Class T%T> _/, Book • M 7 % TO GopyriglitK? SZa COPYRIGHT DEPOSm ELEMENTS OF ENGINEERING THERMODYNAMICS BY JAMES A. MOYER Director of the Massachusetts Department of University Extension formerly Professor of Mechanical Engineering in the Pennsylvania State College JAMES P. CALDERWOOD Professor of Mechanical Engineering in the Kansas State Agricultural College ANDREY A. POTTER Dean of Engineering at Purdue University, formerly Dean of Engineering at the Kansas State Agricultural College NEW YORK JOHN WILEY & SONS, Inc. London: CHAPMAN & HALL, Limited 1920 < 3^ Copyright, 1920, by JAMES A. MOYER, JAMES P. CALDERWOOD AND ANDREY A. POTTER £o-/t$te Manufactured in the U.S.A. CCT I5IS20 ©CI.A576885 PREFACE This treatise is an extension of a briefer work entitled " Engi- neering Thermodynamics" by James A. Moyer and James P. Calderwood. The additions and changes are made to suit the needs of those who had successful experience in using the original publication and found it desirable to add supplementary material to make it sufficiently inclusive for special institutional require- ments. A great deal of the new material is supplied by A. A. Potter. This book is intended to bring out the fundamental principles of Engineering Thermodynamics, and is particularly intended for use in technical colleges where it is possible to give special courses on the subjects of steam turbines, internal combustion engines, refrigeration and other applications of thermody- namics. The new material includes the theory of the hot air engine and internal combustion engine cycles. The appendix includes logarithmic tables, the properties of gases, the properties of steam, ammonia, sulphur dioxide and carbon dioxide. Every engineering student should become familiar with stand- ard works on the subject of thermodynamics. This book should consequently be supplemented by references to standard works on this subject. A representative list of such reference books is given in a table of the appendix. The authors are particularly indebted to the following pro- fessors and instructors in Mechanical Engineering Departments who gave valuable suggestions and criticisms: Edwin A. Fessen- den, Pennsylvania State College; J. E. Emswiler, University of Michigan; G. L. Christensen, Michigan College of Mines; Roy in IV PREFACE B. Fehr, formerly of Pennsylvania State College; H. L. Seward, Yale University; J. R. Wharton, University of Missouri; and J. J. Wilmore, Alabama Polytechnic Institute. J. A. MOYER, J. P. CALDERWOOD, A. A. POTTER. CONTENTS Pages Chapter I. — Thermodynamic Principles and Definitions 1-13 Definition, Scope and Object of Thermodynamics; Heat; Temperature; Thermometers; Absolute Zero; Units of Heat; Specific Heat; Pressure; Volume; Work; Power; Indicated Horse-power; Brake Horse-power; Mechanical Equivalent of Heat; First Law of Thermodynamics; Second Law of Thermodynamics; Effects of Heat Application; The Heat Engine; Thermal Efficiency of a Heat Engine; Problems. Chapter II. — Properties of Perfect Gases 14-25 Perfect Gas Defined; Relation between Pressure, Volume, and Temper- ature of a Perfect Gas; Boyle's Law; Charles' Law; Combination of Boyle's and Charles' Laws; The Law of Perfect Gases; Heat and its Effect upon a Gas; External Work; Internal Energy; Joule's Law; Relation of Specific Heats and the Gas Constant; Ratio of the Two Specific Heats; Values of the Specific Heats; Problems. Chapter III. — Expansion and Compression of Gases 26-39 Expansion at Constant Pressure; Expansion at Constant Volume; Expansion at Constant Temperature, or Isothermal; Adiabatic Expan- sion and Compression; Change of Internal Energy during Adiabatic Processes; Relation between Volume, Pressure and Temperature in Adiabatic Expansion of a Perfect Gas; Problems. Chapter IV. — Cycles of Heat Engines using Gas 40-61 (1) The Carnot Cycle; Reversible Cycles. (2) Hot Air Engine Cycle. The Stirling Engine; The Ericsson Engine. (3) Internal Combustion Engine Cycles. The Lenoir Engine; The Otto Cycle; The Brayton Cycle; the Diesel Cycle. Problems. Chapter V. — Properties of Vapors 62-90 Saturated and Superheated Vapors; Theory of Vaporization; Vapor Tables; Relation between Temperature, Pressure and Volume of Satu- rated Steam; Heat in the Liquid (Water); Latent Heat of Evaporation; External Work of Evaporation; Total Heat of Steam; Internal Energy of Evaporation and of Steam; Steam formed at Constant Volume; Wet Steam; Superheated Steam; Drying of Steam by Throttling or Wire- VI CONTENTS i • ^ • , , Pages drawing; Determination of the Moisture in Steam; Throttling or Superheating Calorimeter; Barrus Throttling Calorimeter; Separating Calorimeters; Condensing or Barrel Calorimeter; Equivalent Evapo- ration and Factor of Evaporation; Vapors as Refrigerating Media; Problems. Chapter VI. — Entropy 91-103 Entropy Changes during Constant Pressure Expansions of Gases; Entropy Changes of Gases at Constant Volume; Entropy Changes during Isothermal Processes of a Gas; Entropy Changes during Reversible Adiabatic Processes of Gases; Entropy Changes during a Carnot Cycle; Temperature-Entropy Diagrams for Steam; Calculation of Entropy for Steam; Total Entropy of Steam; The Mollier Chart; Temperature- Entropy Diagram for the Steam Power Plant; Problems. Chapter VII. — Expansion and Compression of Vapors 104-116 Expansion of Wet Steam at Constant Volume; Expansion of Super- heated Steam at Constant Volume; Expansion at Constant Pressure; Isothermal Lines of Steam; Adiabatic Lines for Steam; Quality of Steam during Adiabatic Expansion; Graphical Determination of Quality of Steam by Throttling Calorimeter and Total Heat-Entropy Diagram; Poly tropic Expansion (n = 1); Problems. Chapter VIII. — Cycles of Heat Engines using Vapors 11 7-149 Carnot Cycle; Rankine Cycle; Practical or Actual Steam Engine Cycle; Efficiency of an Engine Using Steam Without Expansion; Adiabatic Expansion and Available Energy; Available Energy of Wet Steam; Available Energy of Superheated Steam; Application of Temperature- Entropy Diagram to Analysis of Steam Engine; Combined Indicator Card of Compound Engine; Hirn's Analysis; Clayton's Analysis; Prob- lems. Chapter IX. — Flow of Fluids 150-177 Flow Through a Nozzle or Orifice; Weight per Cubic Foot; Maximum Discharge; Shape of Nozzle; Flow of Air Through an Orifice; Receiver Method of Measuring Air; Flow of Vapors; Velocity of Flow as Affected by Radiation; Friction Loss in a Nozzle; Impulse Nozzles; Turbine Losses; Reaction Nozzles; Coefficient of Flow; Injectors; Weight of Feed Water Supplied by an Injector per Pound of Steam; Thermal Effi- ciency of an Injector; Mechanical Efficiency of an Injector; Orifice Measurements of the Flow of Steam; Flow of Steam Through Nozzles; Flow of Steam when the Final Pressure is more than 0.58 of the Initial Pressure; Length of Nozzles; Efficiency of Nozzles; Under- and Over- Expansion; Non-expanding Nozzles; Materials for Nozzles; Problems. CONTENTS VU Page Chapter X. — Applications of Thermodynamics to Compressed Atr and Refrigerating Machinery 178-196 Compressed Air; Air Compressors; Work of Compression; Effect of Clearance upon Volumetric Efficiency; Two Stage Compression; Re- frigerating Machines or Heat Pumps; Unit of Refrigeration; Systems of Mechanical Refrigeration; The Air System of Refrigeration; The Vapor Compression System of Refrigeration; The Vapor Absorption System of Refrigeration; Coefficient of Performance of Refrigerating Machines; Problems. SYMBOLS A = area in square feet, also used to represent the reciprocal of the mechanical equivalent of heat, y-fg-. B.t.u. = British thermal units (= 778 ft.-lbs.). Cp = specific heat at constant pressure in B.t.u. per pound per degree. Cv = specific heat at constant volume in B.t.u. per pound per degree. C = a general constant in equations of perfect gases. E = external work in B.t.u. per pound; also sometimes used to express effi- ciency, usually as a decimal. E a = available energy in B.t.u. per pound. F = force in pounds. H = heat per pound in B.t.u.* Hsup. = total heat of superheated steam, B.t.u. per pound. In = total internal energy of steam (above 32 F.) in B.t.u. per pound, some- times designated by E and i". I L = internal energy of evaporation of steam in B.t.u. per pound, sometimes designated by p. J = mechanical equivalent of heat = 778 (use becoming obsolete). K = specific heat in foot-pound units. L = latent heat of evaporation in B.t.u. per pound. P = pressure in general or pressure in pounds per square foot. Q = quantity of heat in B.t.u. R = thermodynamic constant for gases; for air it is 53.3 (in foot-pound units per pound.) T = absolute temperature, in Fahr. degrees = 460 + t. V = volume in cubic feet, also specific volume and velocity in feet per second. W = work done in foot-pounds. a = area in square inches. c = constant of integration. d = distance in feet. e = subscript to represent base of natural logarithms. g = acceleration due to gravity = 32.2 feet per second per second. h = heat of the liquid per pound in B.t.u. (above 32 ° F.) also designated by q and i' . i' = heat of liquid in B.t.u. per pound (above 32 F.). i" = total internal energy of steam. k = a constant, log = logarithm to base 10. loge = logarithm to natural base e (Naperian). * In steam tables it is total heat above 32° F. ix SYMBOLS n = general exponent for V (volume) in equations of perfect gases, also some- times used for entropy of the liquid in B.t.u. per degree of absolute tem- perature. p = pressure in pounds per square inch. q = sometimes used for heat of the liquid in B.t.u. per pound (above 3 2° F.). r = ratio of expansion also sometimes used for latent heat of evaporation in B.t.u. per pound. s' = entropy of the liquid. s" = total entropy of vapors. t = temperature in ordinary Fahr. degrees. u = difference between the specific volume of a vapor and that of the liquid from which it is formed. v = specific volume, in cubic feet per pound (in some steam tables) . w = weight per cubic foot = density, also used to designate weight of a sub- stance in pounds. x = quality of steam expressed as a decimal. r< y = ratio of specific heats — . Cp 4> = total entropy -^f, sometimes designated by S". 6 — entropy of the liquid in B.t.u. per pound per degree of absolute tem- perature, p = internal energy of evaporation, B.t.u. per pound. °°° Brake Horse Power represents the actual power which an engine can deliver for the purposes of work. The difference between indicated and brake horse power of an engine represents the horse power lost in friction. The brake horse power can be measured by some form of friction brake, which absorbs the power measured, and is called an absorption dynamometer, or by a transmission dynamometer. In either type of dynamometer, if F is the effective pull in pounds, L the lever arm, in feet, through which the weight is exerted, and N the number of revo- lutions of the shaft per minute, the brake horse power is -,, 2TFLN , , B.h.p. = (10) 33>°°° • Mechanical Equivalent of Heat. There is a definite quantita- tive relation between work expended and heat produced. This relation between heat and work is called the mechanical equiva- lent of heat and is designated by /. In the English system, J = 778 foot-pounds or 1 B.t.u. =778 foot-pounds. EFFECTS OF HEAT APPLICATION 9 In the metric system, / = 427 kilogrammeters or 1 calorie = 427 kilogrammeters. The reciprocal of J, or the heat equivalent of work, is designated by A. where A = — - in the English system or in the metric 778 6 427 system. First Law of Thermodynamics. The statement of the definite relation between heat and mechanical work constitutes what is known as the first law of thermodynamics. It is usually expressed: "Heat and mechanical energy are mutually convertible and heat requires for its production and produces by its disappear- ance mechanical work in the ratio of the mechanical equivalent of heat." In other words, this law is a statement of the conserva- tion of energy as regards the equivalence of mechanical work and heat. Second Law of Thermodynamics. "In order to transform the heat of a body into work, heat must pass from that body into another at a lower temperature." Thus, there must be a dif- ference of level in the transformation of heat energy into work and heat cannot be transformed from one body to another at a higher temperature, unless work is expended in order to produce such a transfer of heat. This law states as regards heat engines the limits to their pos- sible performance, which would be otherwise unlimited, if only the "first law" of thermodynamics is considered. It means, also, that no heat engine converts or can convert into work all of the heat supplied to it. A very large part of the heat supplied is necessarily rejected by the engine in the form of unused heat. Effects of Heat Application. If a quantity of heat Q is im- parted to a body, the following effects will be produced: 1. The temperature of the body will rise; 2. The volume of the body will increase; 3. The body will be capable of doing external work. IO THERMODYNAMIC PRINCIPLES AND DEFINITIONS Representing the above effects by S, V and W, Q = S+V + W, (n) in which S represents that quantity of heat, termed the sensible heat, which was utilized in raising the temperature of the body; V represents that quantity of heat which was absorbed by the body in increasing its store of internal energy other than that associated with the sensible heat; and W is the heat which was absorbed to perform the external work in increasing the volume of the body against the resistance offered by external substances. S + V represents that portion of the heat that was chargeable to the increase of internal work. This may be termed the intrinsic energy increase and designated by /. Thus, for the addition of an infinitesimal quantity of heat, dQ = dI + dW or Q = | ~dl - f *PdV. (12) In equation (12), which represents the effect of heat application, the intrinsic energy change / dl depends on the physical state of the body, that is, whether it is a solid, a liquid, a vapor, or a /■» V-t P dV depends on the char- Vi acter of the path in the work diagram. The Heat Engine. The heat engine is a machine which con- verts the heat energy of solid, liquid or gaseous fuel into work. This conversion depends on the variation in the pressure, volume and temperature of a gas or a vapor and can be accomplished in two ways: First, by "external combustion," in which case the fuel is burned outside of the engine cylinder; the heat developed by the combustion of the fuel is conducted to the working substance or heat medium through walls; this working substance does work on a piston in the case of a reciprocating engine or on a vane or THERMAL EFFICIENCY OF A HEAT ENGINE n " blade " in a turbine. To this class belong steam engines of the reciprocating, turbine or rotary types and also external-combus- tion hot air engines. Thus, in the case of the steam engine, the fuel, which may be coal, wood, petroleum or gas, is burned out- side of the boiler shell and the resulting heat is transmitted by conduction through the metal of the shell to the working sub- stance, which is water. When enough heat has been added to the water to produce a change in its physical state, water vapor or steam is formed at the required pressure. This vapor, which may be dry, wet or superheated, if allowed to act on the piston of the engine, will do work. Another method of converting heat into mechanical energy is by burning the fuel rapidly or slowly inside of an engine cylinder or in a communicating vessel, the products of combustion being allowed to act directly on the piston of the engine. To this class belong gas, petroleum and alcohol engines which are called " internal combustion " engines. Thermal Efficiency of a Heat Engine. By thermal efficiency (E) is meant the ratio of the heat converted into work (AW) to the heat supplied by the engine (Qi), or 77 AW E - -^-. (13) Since only a part of the heat supplied to an engine can be con- verted into work, the above ratio is a fraction always less than unity. PROBLEMS 1. Give examples of the transfer of heat by conduction, radiation and convection. 2. Show that the kilogram calories per kilogram X 1.8 give B.t.u. per pound. 3. Prove that the product of a pressure in pounds per square foot and a volume in cubic feet results in foot-pounds of work. 4. If the specific heat of a substance is 0.65, how many B.t.u. are re- quired to raise the temperature of 10 lbs. of the substance through io° F.? 5. The specific heat of a substance is expressed by the equation, C = O.S — O.C2 t. 12 THERMODYNAMIC PRINCIPLES AND DEFINITIONS What heat is required to raise the temperature of 5 lbs. of the substance from io° to ioo° F.? 6. Convert — 40 C. into degrees Fahrenheit. 7. Change 350 F., 212 F. and 160 C. to absolute Fahrenheit tempera- tures. 8. Prove that the weight of 1 cu. in. of mercury is equal to 0.491 lb. 9. If the barometric reading is 29.2 ins., change 140 lbs. per sq. in. gage and also 27 ins. vacuum into pounds per square inch absolute pressure. 10. Calculate the indicated horse power of a 12" X 13" steam engine which operates at a speed of 265 r.p.m. The mean effective pressure of the head end is 27.5 lbs. per sq. in. and of the crank end 27.8 lbs. per sq. in. The diameter of the piston rod is 1 f inches. 11. Calculate the brake horse power developed by an engine as measured by a Prony brake, the effective pull being 32 lbs. at 250 r.p.m. and the lever arm 32 inches long. 12. One pound of fuel has a heating value of 14,500 B.t.u. How many foot-pounds of work is it capable of producing, if all this heat is converted into work? 13. An engine developed 15,560 foot-pounds of work. How much heat in B.t.u. was theoretically required? 14. A heat engine receives 100,000 B.t.u. of heat in the form of fuel and during the same period 30,000 B.t.u. are converted into work. What per- centage (thermal efficiency) of the heat received by the engine was converted into work? 15. A gas engine receives 20,000 B.t.u. of heat in the form of fuel and during the same period 3,11 2,000 foot-pounds of work are developed. What is the thermal efficiency of the engine? 16. It is claimed that a certain motor generates 300,000 foot-pounds of work per hour and during this period receives 400 B.t.u. of heat in the form of fuel. Are such results possible? 17. An oil engine uses 0.74 lb. of fuel per b.h.p. per hour. Calculate the thermal efficiency of this engine if the oil has a calorific value of 18,600 B.t.u. per lb. 18. An engine receives 200 B.t.u. of heat per minute and exhausts during the same period 100 B.t.u. If no losses of heat occur within the cylinder, (a) How many B.t.u. of heat are being transformed into work? (b) What number of foot-pounds does this heat produce? (c) What horse power is being developed? (d) What is the thermal efficiency of the engine? 19. In the manufacture of certain explosives, acids are mixed with an oxidizable substance. During the process the mixture must be constantly agitated by a stirring mechanism to maintain uniform conditions, and the PROBLEMS 13 temperature of the mixture must be kept below a certain predetermined value to prevent explosion. If during the process of manufacture 5000 foot-pounds of work are delivered per minute to the agitator, and 1000 B.t.u. are generated during the same period by the chemical reaction, how much heat must be absorbed per hour to maintain the temperature of the mixture constant? 20. Prove that one horse power developed for one hour is equivalent to the consumption of 2545 B.t.u. of heat in the same period. CHAPTER II PROPERTIES OF PERFECT GASES In the study of thermodynamics, the working substance, or heat medium, through which the heat engine converts heat into work, is in the condition of a perfect gas or vapor. The laws governing the action of the two classes of substances differ. For this reason the study of thermodynamics is divided into the thermodynamics of gases and of vapors. When the term " gas " is used it refers to what is more properly called a perfect gas. A perfect gas may be defined as a fluid which remains in the gaseous state when subjected to changes in pressure or in temperature. Gases which are near their point of condensation are not perfect gases. Oxygen, hydrogen, nitro- gen, air and carbon dioxide are practical examples of perfect gases. Vapors are fluids which are readily transformed into liquids by a very moderate reduction in temperature or increase in pressure. Common examples of vapors are steam and ammonia. Relation between Pressure, Vol- ume and Temperature of a Per- fect Gas. In practically all heat engines, work is done by changes of volume of a fluid, and the amount of work performed depends only on the relation of pressure to volume during such change and not at all on the form of the vessel containing this fluid. Figure 2 shows a vessel containing a perfect gas and surrounded by a jacket filled with cracked ice. Its temperature will, there- 14 Connection to Air Pump WJUIMEWa Fig — Constant Temperature Apparatus for Demonstrating Relation between Pressure and Volume of a Gas. BOYLE'S LAW 1 5 fore, be at 32 F. This vessel has a tightly fitting piston P of which the lower flat side has an area of one square foot. In the position shown the piston is two feet from the bottom of the vessel, so that the volume between the piston and the bottom of the vessel is two cubic feet. The pressure on the gas is that due to the piston and the weights shown. Assume this total weight is 100 pounds and that the air pump connected to the top of the vessel maintains a vacuum above the piston. Then the pressure on the gas below the piston is 100 pounds per square foot. If now the weights are increased to make the pressure on the gas 200 pounds per square foot the piston will sink down until it is only one foot from the bottom of the vessel, provided the ice keeps a constant temperature. If the temperature is not maintained constant, because of the tendency of gases to expand with in- crease in temperature, it will be necessary to apply a total weight greater than 200 pounds to reduce the volume to one cubic foot. Similarly, if the weight on the gas were reduced to 50 pounds and the vessel were made high enough, the lower side of the piston would then be four feet from the bottom of the vessel. Examination of the above figures shows that if the temperature is constant the product of pressure and volume is a constant, and in this particular case it is always equal to 200 foot-pounds. These facts are expressed by Boyle's Law which can be stated as follows : Boyle's Law. If a unit weight of gas is compressed or ex- panded at constant temperature, the pressure varies inversely as the volume, or the product of pressure and volume remains a constant. Thus, if P h V± are the initial pressure and volume and P 2 , V 2 the final pressure and volume, PiV 1 = P 2 V 2 . (14) The laws of thermodynamics dealing with volume and pressure changes corresponding to temperature variations may be stated as follows: (1) Under constant pressure the volume of a given mass of gas varies directly as the absolute temperature. 16 PROPERTIES OF PERFECT GASES (2) Under constant volume the absolute pressure of a given mass of gas varies directly as the absolute temperature. These fundamental principles, often called Gay-Lussac's or Charles* Laws, may also be stated thus: V T With pressure constant, — - = — -, (15) V 2 T 2 p j» With volume constant, — - = — -, (16) "2 1 2 where V\ and V 2 are respectively the initial and final volumes, Pi and P 2 are the initial and final absolute pressures, and 7\ and T 2 are the absolute temperatures corresponding to the pressures and volumes of the same subscripts. The following problem shows applications of Charles' laws: A gas has a volume of 2 cubic feet, a pressure of 14.7 pounds per square inch absolute and a temperature of 6o° F. (a) What will be the volume of this gas if the temperature is increased to 120 F., the pressure remaining constant? (b) What will be the pressure if the temperature is increased as in (a) but the volume remains constant? Solution, (a) Since the pressure remains constant and the substance is a gas, the volume varies directly as the absolute temperature. Letting Vi and T\ be the initial conditions and V 2 and T 2 be the final conditions, then 60 + 460 120 + 460' V 2 = 2.23 cubic feet. (b) Since the volume remains constant, Pi T\ 14.7 60 + 460 or V, T, 2 or v 2 T 2 v 2 P 2 T 2 P 2 120 + 460* P 2 = 16.39 pounds per square inch absolute. Combination of Boyle's and Charles' Laws. Equations (14), (15), and (16) cannot often be used as they stand, because it COMBINATION OF BOYLE'S AND CHARLES' LAWS 17 does not often happen that any one of the three variables (P, V and P) remains constant. A more general law must be developed, therefore, allowing for variations in all of the terms P, V and P. This is accomplished by combining the above equations. Assume a pound of gas of which the initial conditions of pres- sure, volume and temperature are represented by P h Vi and T 1} while the corresponding final conditions are given by P 2 , V 2 and P 2 . The first step is in changing the volume from Vi to V 2 and the pressure from Pi to some intervening pressure Pi while the temperature Pi remains constant. This change can be expressed by Boyle's law (equation 14). With constant temperature (Pi), from which, by solving, V, Pi v 2 = pT (i7) Pi = ^ ( l8 ) where Pi is the resulting pressure of the gas when its volume is changed from Vi to V 2 , with the temperature remaining constant at Pi. The second step is in the change in pressure from Pi to P 2 and in temperature from Pi to T 2 , while the volume remains con- stant at V 2 . This step is expressed as follows: With constant volume (T 2 ), Pi Pi / \ T, = T,' (l9) which may be written D P 2 T 2 , x P2 = ~y— (20) Substituting now the value of Pi from (18) in (20), we have P > = -F5T.' (2l) 1 8 PROPERTIES OF PERFECT GASES which may be arranged to read, P1V1 P2V2 (22) The following problem shows the application of equation (22): A quantity of air at atmospheric pressure has a volume of 2000 cubic feet when the barometer reads 28.80 inches of mercury and the temperature is 40 C. What will be the volume of this air at a temperature of o°C. when the barometer reads 29.96 inches of mercury? Solution. Volume, pressure and temperature vary in this case as in the following equation, P1F1 P 2 V 2 then T x T 2 Letting P h Vi, T\ = initial conditions, P2, V 2) T 2 = final conditions, 28.80 X 2000 29.96 X V 2 40 + 273 o + 273 V 2 = 1676 cubic feet. Now, since P 2 , V 2 and T 2 in equation (22) represent any simultaneous condition of the gas, we may also write the follow- ing more general relations: PiVx P 2 V 2 P 3 V = a constant, (23) 2\ T 2 T 3 and, therefore, PV = RT, (24) PV where R is the " gas constant," and is equal to — - The Law of Perfect Gases. Equation (24) expresses the law connecting the relation between pressure, volume and tempera- ture of a perfect gas. In this equation V is the specific volume, or the volume occupied by a unit weight of a gas at the absolute pressure P and absolute temperature T; R is the gas constant THE LAW OF PERFECT GASES 19 in foot-pounds and depends on the density of the gas and on the units of measurement adopted. By means of equation (24) if the pressure, volume and tem- perature of a gas for one given condition are known, the value of R can be determined. Example 1. If the volume of air at freezing point and atmos- pheric pressure is 12.39 cubic feet per pound, calculate the value of R in the English units. Solution.. R = M* = I4 -7 X 144 X 12.39 _ 5 . To 32 + 460 Example 2. If one pound of air occupies 5 cubic feet at a temperature of 200 F., find the corresponding pressure. Solution. Using the value of R for air as calculated above „ RTi ^.3 (460 + 200) , Px = — — = °° ° v ^ - = 7040 pounds Vi 5 per square foot absolute, which is the same as 34.2 pounds per square inch gage pressure. In calculating R by equation (24) care must be taken not to confuse the units of measurement. It must also be remembered that the method, as illustrated in the above examples, gives the value of R for one pound of air, or for one unit weight of the gas in question; for w pounds, the value of the constant is wR, or: PV = wRT, (25) where P = absolute pressure in pounds per square foot, V = volume in cubic feet, w = weight of gas in pounds, R = the "gas constant" for one pound of gas in foot- pound units, T = the absolute temperature in Fahrenheit degrees. This equation is applicable to any perfect gas within the limits of pressure and temperature employed in common engineering practice. The " thermodynamic" state of a gas is known when its pressure, volume, temperature, weight and composition are known; when any four of these quantities are known the fifth can be found by equation (25). 20 PROPERTIES OF PERFECT GASES Heat and Its Effect Upon a Gas. In equation (12) it was shown that in general the effect of adding heat upon a substance was to increase the intrinsic energy and to overcome the external resistances producing work. This law can be stated as follows: Heat supplied = increase in intrinsic energy + the external work done. The converse of this statement is equally true. The heat abstracted from a gas equals the decrease in intrinsic energy plus the negative work done. External Work. The external work or the work done by a gas in its expansion is represented graphically by Fig. 3. The area under the expansion line BC ^/w//w//m;w;mm//m/z Pi i 1 I • 1 1 1 B C Sm 3 !/J Cfl V u Qui is proportional to the work done "^ in the expansion. If the initial condition of the gas at B as re- gards pressure and volume is rep- resented by Pi and Vi and the final condition at C by Pi and V 2 (expansion being at constant pres- Vi V 2 sure), the force P moved through Volume / N a distance of abscissas (k 2 — m) Fig. 3. -External Work of Expansion. is & measure of the WQrk done> Obviously the area under the line BC divided by the horizontal length (V 2 — Vi) is the average value of the force P. If, further, and in general, we represent the area under BC by the symbol A, then we can write, — — = average value of P, V 2 — ML whether or not P is constant. And also, Work done = A T _ X (7 2 - Fi) = A. The same principle applies whether the line BC is a straight line, as shown in Fig. 3, or a very irregular curve, as will be shown later. INTERNAL ENERGY 21 Internal Energy. The heat energy possessed by a gas or vapor, or the heat energy which is contained in a gas or vapor in a form similar to " potential " energy, is called its internal energy. It is also called intrinsic energy, since it may be said to " reside " within the substance and has not been transferred to any other substance. Thus, an amount of heat added to a substance when no work is performed is all added to the internal energy of that substance. On the other hand, when heat is added while work is being performed, the internal energy is increased only by the difference between the heat added and the work done. Internal energy may also be denned as the energy which a gas or vapor possesses by virtue of its temperature, and for one pound of gas may be expressed as follows : Internal energy '= C v dT (in B.t.u.), where T is the absolute temperature and C v the specific heat at constant volume. From the paragraph on specific heat it will be remembered that C v takes into account only that heat required to raise the temperature, since under constant volume conditions no external work is done; and, therefore, in dealing with internal energy, C v is always used. Increase in internal energy in B.t.u. (for one pound of a gas) = C v (r 2 - 2\). (26) Joule's Law. In the case of ideally perfect gases, such as thermodynamic equations must deal with, it is assumed, when a gas expands without doing external work and without taking in or giving out heat (and, therefore, without changing its stock of internal energy), that its temperature does not change. It was for a long time supposed that when a gas expanded without doing work, and without taking in or giving out heat, that its tempera- ture did not change. This fact was based on the famous experi- ments of Joule. Later investigations by Lord Kelvin and Linde have shown that this statement is not exactly correct as all known gases show a change in temperature under these conditions. This change in temperature is known as the " Joule-Thomson" effect. 22 PROPERTIES OF PERFECT GASES Relation of Specific Heats and the Gas Constant. If heat is added at constant pressure, then Q = wC P (T 2 - 7\). (27) Also, by equation (26), the increase in internal energy when heat is added = wC,(T 2 - 7\). (28) External work = P (V 2 — Vi) foot-pounds - P (F2 7 Fl) B.t.u. (2 9 ) 778 yy Since the heat added = increase in internal energy + external work, wc p (t 2 - ro = wc v (t 2 - r x ) + ISXi^JA. ( 3o) 778 By equation (25), P 2 V 2 = wRT 2 and P X V X = wRTl Substituting these values in (30), wC p (T 2 - - Ti) = wC v (T 2 — Ti) + w — 778 - (31) Simplifying, C = C 4- • (32) C P -C =—= AR. 778 (33) Equation (33) shows that the difference between the two specific heats is equal to the gas constant R, which when measured in foot-pounds represents the external work done by one pound of a gas when its temperature is increased by one degree under constant pressure. Example. The specific heat of air at constant pressure (C p ) is 0.2375 B.t.u. and R = 53.3 foot-pounds. Calculate the spe- cific heat at constant volume (C») . Solution. C v = C p — AR = 0.2375 — ^|- = 0.1690 B.t.u. 778 RATIO OF THE TWO SPECIFIC HEATS 2 3 Ratio of the Two Specific Heats (^r). The constant repre- senting the ratio of the two specific heats of a perfect gas is represented by 7 where n/ = — =- J ( \ 7 C v r AR AR K34) Example. Calculate the value of 7 for air. C v = 0.2375 B.t.u. R = 53.3 foot-pounds. Solution. 7 = r— = = 1.40s. j -AR T 53-3 C p 778 x 0.2375 The constant designating the relation between the specific heats of air is often designated by k instead of 7. Values of the Specific Heats. Regnault after carrying on experiments on the specific heat of hydrogen, oxygen, air and •carbon dioxide concluded that all gases have a constant specific heat under varying pressures and temperatures. Recent experi- ments ' tend to show that the specific heats of substances vary with the pressure and temperature. The variability in the values of the specific heats does not influence to any very great extent most thermodynamic computations. In the application of thermodynamics to internal combustion engines the exact values of the specific heats are of considerable importance. Tables 1 and 2 in the appendix give constants for various gases. PROBLEMS 1. Air at constant pressure with an initial volume of 2 cu. ft. and temper- ature of 6o° F. is heated until the volume is doubled. What is the resulting temperature in degrees Fahrenheit? 2. Air is cooled at constant volume. The initial pressure is 30 lbs. per 24 PROPERTIES OF PERFECT GASES sq. in. absolute and the initial temperature is ioi° F. The final condition has a temperature of 50 F. What is the final pressure? 3. One pound of hydrogen is cooled at constant pressure from a volume of 1 cu. ft. and temperature of 300 F. to a temperature of 6o° F. What is the resulting volume? 4. A tank whose volume is 50 cu. ft. contains air at 105 lbs. per sq. in. absolute pressure and temperature of 8o° F. How many pounds of air does the tank contain? 5. An automobile tire has a mean diameter of 34 inches and a width of 4 inches. It is pumped to 80 lbs. per sq. in. gage pressure at a temperature of 6o° F.; atmospheric pressure 14.6 lbs. per sq. in. absolute. (a) How many pounds of air does the tire contain? (b) Assuming no change of volume, what would be the gage pressure of the tire if placed in the sun at ioo° F.? 6. A gas tank is to be made to hold 0.25 lb. of acetylene when the pres- sure is 250 lbs. per sq. in. gage, atmospheric pressure 14.4 lbs. per sq. in. absolute, and the temperature of the gas 70 F. What will be its volume in cubic feet? 7. A quantity of air at a temperature of 70 F. and a pressure of 15 lbs. per sq. in. absolute has a volume of 5 cu. ft. What is the volume of the same air when the pressure is changed at constant temperature to 60 lbs. per sq. in. absolute? 8. How many pounds of air are required for the conditions in problem 7? 9. The volume of a quantity of air is 10 cu. ft. at a temperature of 6o° F. when the pressure is 15 lbs. per sq. in. absolute. What is the pressure of this air when the volume becomes 60 cu. ft. and the temperature 6o° F.? 10. How many pounds of air are required for the conditions in problem 9? 11. A tank contains 200 cu. ft. of air at a temperature of 6o° F. and under a pressure of 200 lbs. per sq. in. absolute. (a) What weight of air is present? (b) How many cubic feet will this air occupy at 14.7 lbs. per sq. in. absolute and at a temperature of ioo° F.? 12. The volume of a quantity of air at 70 F. and at a pressure of 14.2 lbs. per sq. in. absolute is 20 cu. ft. What is the temperature of this air when the volume becomes 5 cu. ft. and the pressure 80 lbs. per sq. in. absolute? 13. If the specific heat of carbon dioxide under constant pressure C v is 0.2012 and the value of R is 35.10, find the value of the specific heat under constant volume C v . 14. How many B.t.u. are required to double the volume of one pound of air at constant pressure from 50 F. 15. A tank filled with 200 cu. ft. of air at 15 lbs. per sq. in. absolute and 6o° F. is heated to 150 F. PROBLEMS 25 (a) What will be the resulting air pressure in the tank? (b) How many B.t.u. will be required to heat the air? 16. A tank contains 200 cu. ft. of air at 6o° F. and 40 lbs. per sq. in. abso- lute. If 500 B.t.u. of heat are added to it, what will be the resulting pres- sure and temperature? CHAPTER III EXPANSION AND COMPRESSION OF GASES The equation of the perfect gas in the form PV = wRT for the expansion or compression of gases has three related variables, (i) pressure, (2) volume and (3) temperature. For a given weight of gas with any two of these variables known the third is fixed. As regards the analysis of the action of heat engines, the pressure and volume relations are most important, and graphical diagrams, called pressure-volume or P-V diagrams, are frequently needed to assist in the analysis. The indicator diagram is a pres- sure-volume diagram drawn autographically by the mechanism of an engine indicator. A pressure- volume diagram is shown in Fig. 4, in which the vertical scale of coordinates represents pressures and the horizontal, ^ volumes. Assume that the pres- '^'m 1 ^ V3 7 Vl ~ v * sure and volume of a pound of a « gas are given by the coordinates P and Vi, which are plotted in the middle of the diagram. It & 24 6 8 io will be assumed further that Volume, eu. ft. the pressure remains constant in Fig. 4. — Diagram of Expansion and , , -, i • 1 • 1 ~ . . r, , . t> the changes to be indicated. Compression at Constant Pressure. to Now if the gas is expanded until its volume becomes V 2 , then its condition as regards pressure and volume would be represented by P Vi. If, on the other hand, the gas had been compressed while a constant pressure was maintained, its final condition would be represented by the point PVz to the left of PV\. Similarly, any line whether straight or curved extending from the initial condition of the gas at PV\ will represent an expansion when drawn in the direction away 26 CD EXPANSION AT CONSTANT PRESSURE 27 from the zero of volumes and will represent a compression when tending toward the same zero. It has been shown (page 20) that areas on such diagrams repre- sent the product of pressure and volume, and, therefore, work or energy. Thus in Fig. 4 the area under the curve PV 3 to PV 2 represents on the scales given 100 (pounds per square foot) X (9 — 1) cubic feet or 800 foot-pounds irrespective of whether it is an expansion or a compression from the initial condition. Most of the lines to be studied in heat engine diagrams are either straight or else they can be exactly or approximately represented by an equation in the form PV n = a, constant, (35) where the index n, as experimentally determined, has varying numerical values, but is constant for any one curve. When the lines of the diagram are straight the areas of simple rectangles and triangles need only be calculated to find the work done. The two most common forms of curves to be dealt with in ex- pansions are (1) when there is expansion with addition of heat at such a rate as to maintain the temperature of the gas con- stant throughout the expansion. Such an expansion is called isothermal. The other important kind of expansion (2) occurs when work is done by the gas without the addition or abstraction of heat. To do this work some of the internal heat energy contained in the gas must be transformed in proportion to the amount of work done. Such an expansion is called adiabatic. The following problems show the application of the foregoing principles to various types of expansions: 1. Expansion at Constant Pressure. One pound of air having an initial temperature of 6o° F. is expanded to ioo° F. under constant pressure. Find (a) External work during expansion; (b) Heat required to produce the expansion. Solution. The heat added equals the increase in internal energy plus the external work done. In solving for the heat added or required during any expansion it is only necessary to 28 EXPANSION AND COMPRESSION OF GASES find the external work (which is equal to the area under the ex- pansion curve) and add to it the heat needed to increase the internal energy. The external work = W = P l (V 2 -V 1 ). (36) Its equivalent is: wR (T 2 — 7\). (37) W = 1 X 53.3 [(100 -f- 460) — (60 + 460)] = 2i32ft.-lbs. The increase in internal energy: I = wC v (T 2 - TO (38) / = I X 0.169 [(100 + 460) — (60 + 460)] = 6.76 B.t.u. Heat required (Q) = 6.75 H — = 9.50 B.t.u. 778 Another method of computing the heat required to produce the expansion is: e = ^c P (r 2 -r 1 ). (39) Q = 1 x 0.237 [( IO ° +.460) — (60 + 460)] = 9.50 B.t.u. approximately. 2. Expansion at Constant Volume. One pound of air having an initial temperature of 6o° F. is heated at constant volume until the final temperature is 120 F. Find: (a) External work; (b) Heat required. » Solution. Heat added (Q) = increase in internal energy -f- external work. External work = o. Then Heat added = increase in internal energy + o = wC v (T 2 - Ti) + o = 1 X 0.169 [(100 + 460) — (60 + 460)] + o = 6.76 B.t.u. 3. Expansion and Compression at Constant Temperature (Isothermal). In an isothermal expansion or compression the ISOTHERMAL EXPANSION AND COMPRESSION 29 temperature of the working substance is kept constant through- out the process. The form of the isothermal curve on pressure- volume coordinates depends upon the substance. In the case of perfect gases Boyle's Law (equation 14) applies and we have: PV = C = a constant. (40) Equation (40) is that of a rectangular hyperbola. It is the special case of the general equation PV n = constant (35), in which the index n = 1 and is represented by Fig. 5. Volume dV Fig. 5. — Work done during Isothermal Expansion and Compression. The external work performed is shown graphically by the shaded area under the curve between A and B (Fig. 5). The two vertical lines close together in the figure are the limits of a narrow closely shaded area and indicate an infinitesimal volume change dV. Work done during this small change of volume is, the JW = P dV, and for a finite change of volume of any size as from V\ to V 2 the work done, W (foot-pounds), is: W PdV. (41) 30 EXPANSION AND COMPRESSION OF GASES For the integration of this form it is necessary to substitute P in terms of V. Assume that P and V are values of pressure and volume for any point on the curve of expansion of a gas of which the equation is PV = C. Then P = £• Substituting this value of P in equation (41), tv *dV Vl v W = C (log. V 2 - loge FO. (42) Since the initial conditions of the gas are Pi and Vi, we have PV = C = PxFi, and substituting this value of C in equation (42), we obtain W = PxFi (log, F 2 - log e 70 or T7 = P1V1 loge :==? (in foot-pounds). (43) r 1 Units of weight do not enter in equations (42) and (43). For a certain weight of gas under the same conditions, since Vo P P1V1 = wRT (in foot-pounds) and — = -=^> Vi P% then the work for w pounds is : V P W = wRT loge — = wRT log e -5^ (in foot-pounds). (44) V I P2 . V* Often the ratio — is called the ratio of expansion and is rep- V\ resented by r. Making this substitution we have, W = wRT log s r. (45) Equations (42), (43), (44) and (45) refer to an expansion from P1V1 to P2V2. If, on the other hand, the work done is the result of a compression from P1V1 to P3V3 the curve of compression ISOTHERMAL EXPANSION AND COMPRESSION 31 would be from A to C and the area under it would be its graphical representation. Equations (43), (44) and (45) would represent the work done for compression the same as for expansion, except that the expression would have a negative value; that is, work is to be done upon the gas to decrease its volume. The isothermal expansion or compression of a perfect gas causes no change in its stock of internal energy since the temper- ature T is constant. During such an expansion the gas must take in an amount of heat just equal to the work it does, and conversely during an isothermal compression it must reject an amount of heat just equal to the work spent upon it. This quantity of heatQ (in B.t.u.) is, from equation (45), n wRT , V 2 t ,, Q = w ge v; (46) The following problem shows the application of the foregoing formulas to isothermal expansions: Air having a pressure of 100 pounds per square inch absolute and a volume of 1 cubic foot expands isothermally to a volume of 4 cubic feet. Find (a) External work of the expansion; (b) Heat required to produce the expansion; (c) Pressure at end of expansion. Solution, (a) Since the expansion is isothermal, External work, W = Pi7i log e * ^ = IOO X 144 X I x 1.3848 = 19,940 foot-pounds. (b) Since the heat added equals increase in internal energy plus external work, and since the temperature remains constant (requiring therefore no heat to increase the internal energy), the internal energy equals zero and the heat added equals the work done. * 2.3 X log base 10 = log base e. Tables of natural logarithms are given in the appendix. 32 EXPANSION AND COMPRESSION OF GASES Then: Heat added = external work = 9>94Q = 25.6 B.t.u. 778 (c) then Since P1V1 100 X 1 P 2 P 2 F 2 , P 2 x 4, 25 pounds per square inch absolute. If a gas expands and does external work without receiving a supply of heat from an external source, it must derive the amount of heat needed to do the work from its own stock of internal energy. This process is then necessarily accompanied by a low- ering of temperature and the expansion obviously is not iso- thermal. 4. Adiabatic Expansion and Compression. In the adiabatic mode of expansion or compression the working substance neither receives nor rejects heat as it expands or is compressed. A curve which shows the relation of pressures to volumes in such a process is called an adiabatic line (see Fig. 6). In any adiabatic Volume Fig. 6. — Isothermal and Adiabatic Expansion Lines. process the substance is neither gaining nor losing heat by conduction, radiation or internal chemical action. Hence the work which a gas does in such an expansion is all done at the expense of its stock of internal energy, and the work which is done upon a gas in such a compression all goes to increase its internal energy. Ideally adiabatic action could be secured by a gas expanding, or being compressed, in a cylinder which in all parts was a perfect non-conductor of heat. The compression of a gas in a cylinder is approximately adiabatic when the process is very rapidly performed, but when done so slowly that the heat ADIABATIC EXPANSION AND COMPRESSION 33 has time to be dissipated by conduction the compression is more nearly isothermal. Fig. 6 shows on a pressure-volume diagram the relation between an isothermal and an adiabatic form of ex- pansion or compression from an initial condition P1V1 at A to final conditions at B and C for expansions, and at D and E for compressions. In order to derive the pressure-volume relation for a gas expanding adiabatically, consider the fundamental equation (page 20): Heat added = increase in internal energy + external work, or: .<2 = wK v (T 2 - TO + PdV (foot-pounds), (47) where K v is the specific heat in foot-pound units, i.e., 778 C v . In the adiabatic expansion no heat is added to or taken away from the gas by conduction or radiation, and, therefore, the left hand member of the above equation becomes zero. Furthermore, since equation (25) can always be applied to perfect gases, the following simultaneous equations may be written: o = wK v dT + P dV, (48) PV = wRT. (49) When P, V and T vary, as they do in adiabatic expansion, equation (49) may be written as follows: PdV+ VdP = wRdT, (50) and PdV + VdP dT = wR Substituting the value of dT in (48), n^T/ , v PdV + VdP , , PdV + wK v l — = o. (51) wR RPdV + K V P dV + K V V dP = o. 34 EXPANSION AND COMPRESSION OF GASES To separate the variables divide by PV: W 4. K dV + K dF p dV dV dP . . R — + K, — + K, — = o. (52) Collecting terms, (i? + K.) ^ + tf. ^ = o. Integrating, (R + K v ) log e F + A% log e P = a constant = c. (53) *±*'log a F + log.P = C . Ay ig + gp lo ge PF * =c, (54) since from equation (^), R + K v = Kp y where K v and A% are respectively the specific heats at constant pressure and at constant volume in foot-pound units, then equa- tion (54) becomes: From equation (34), \og & PV Kv =c. therefore : r~ = y > or k~ = 7 > PV 7 = a constant. (55) Following the method used for obtaining an expression for the work done in isothermal expansion (equation 43), the work done, W (in foot-pounds), for a change of volume from Vi to F 2 , Jf*Vi PdV. (56) W V 2 For purposes of integration, P can be substituted in terms of V as outlined below. In the general expression PV n = c,sl con- stant (see equation 35), where P and V are values of pressure and volume for any point on the curve of expansion of a gas of which ADIABATIC EXPANSION AND COMPRESSION 35 the initial condition is given by the symbols Pi and V h we can then write, p = — (57) And substituting (57) in (56), r v~ n+1 Y 2 L- n + ij 7l = 1 i-„ J (59) Since PV n = c = PiV? = P 2 V 2 n , we can substitute for c in (59) the values corresponding to the subscripts of V as follows: P 2 V 2 n V 2 l ~ n - PiF/% 1 -" W = w = 1 — n P 2 V 2 - P 1 V 1 ) 1 — n or W = ^ ^^ (foot-pounds). (60) n — 1 Since PF = wPP, PT = wR (Tl ~ T2) - (foot-pounds). (61) n — 1 Equations (60) and (61) apply to any gas undergoing expan- sion or compression according to PV n = a constant. In the case of an adiabatic expansion of a perfect gas n = 7 (see equation 55). Change of Internal Energy During Adiabatic Processes. Since in an adiabatic expansion no heat is conducted to or away from the gas, the work is done at the expense of the internal energy and, therefore, the latter decreases by an amount equiva- lent to the amount of work performed. This loss in internal energy is readily computed by equation (60) or (61). The result must be divided by 778 in order to be in B.t.u. During an adiabatic compression the reverse occurs, i.e., there 36 EXPANSION AND COMPRESSION OF GASES is a gain in internal energy and the same formulas apply, the result coming out negative, because work has been done on the gas. Relation between Volume, Pressure and Temperature in Adiabatic Expansion of a Perfect Gas. Since P, V and T vary during an adiabatic expansion, it will be necessary to develop for- mulas for obtaining these various quantities. It will be remem- bered that equation (25), applies to perfect gases at all times. Therefore, in the case of an adiabatic expansion or compression we can write the two simultaneous equations: ■££-.££•• (A) ±1 1 2 p x v x y = p 2 v 2 y . (B) By means of these two equations we can find the final condi- tions of pressure, volume and temperature, having given two initial conditions and one final condition. For instance, having given V\, V 2 and T h to find T 2) divide (A ) by {B), member for member. Then V 1 V 2 TxV^ T 2 V 2 y T 2 = Vj-v T 2 = T,' or In like manner the following formulas can be obtained: (63) p -rM y . («4) ADIABATIC EXPANSION AND COMPRESSION 37 P* = Pi (ffi*. (65) V, = V 1 (^p, (66) 1 Fs=Fl (S) 71 ' (67) It should be noted that the above formulas can be used for any expansion of a perfect gas following PF" = a constant, provided y in the formulas is replaced by n. It is also to be noted that these equations can be used for any system of units so long as the same system of units is employed throughout an equation. There are many cases of expansions which are neither adiabatic nor isothermal and which are not straight lines on P-V diagrams. It will be observed from the equations in the discussion of the internal work done by an expanding gas and for the change of internal energy, that if in the general equation PV n = a. constant the exponent or index n is less than y, the work done is greater than the loss in internal energy. In other words for such a case, the expansion lies between an adiabatic and isothermal and the gas must be taking in heat as it expands. On the other hand, if n is greater than y the work done is less than the loss of internal energy. Example. Given a quantity of pure air in a cylinder at a tem- perature of 6o° F. (7\ = 460 + 60 = 520 degrees absolute) which is suddenly (adiabatically) compressed to half its original volume. Then — 1 = -— , and taking y as 1.405, the temperature immediately V 2 1 after compression is completed, T 2 , is calculated by equation (62) as follows: /FA 7-1 /2V- 405 - 1 T 2 = Ti I y) = 520 I- J = 520 X 2 0405 = 688° absolute, or t 2 in ordinary Fahrenheit is 688 — 460 or 228 degrees. 38 EXPANSION AND COMPRESSION OF GASES The work done in adiabatic compression of cAe pound of this air is calculated by equation (61): w= wRjT.-T,) = 53.3(520-688) = 53-3 (-168) = _ 22jIIQ 7-1 1.405 -1 0.405 foot-pounds per pound of air compressed. The negative sign means that work has been done on the gas or the gas was com- pressed. If the sign had been positive it would have indicated an expansion. As the result of this compression the internal energy of the gas has been increased by — B.t.u., but if the cylinder is a con- _ 778 ductor of heat, as in practice it always is, the whole of this heat will become dissipated in time by conduction to surrounding air and other bodies, and the internal energy will gradually return to its original value as the temperature of the gas comes back to the initial temperature of 6o° F. PROBLEMS 1. Calculate the heat required to produce a temperature change of 50 F. in three pounds of air at constant pressure. 2. How many foot-pounds of work are done by 2 lbs. of air in expand- ing to double its volume at a constant temperature of ioo° F.? 3. Three pounds of air are to be compressed from a volume of 2 to 1 cu. ft. at a constant temperature of 6o° F. How many B.t.u. of heat must be rejected from the air? 4. An air compressor has a cylinder volume of 2 cu. ft. If it takes air at 14.4 lbs. per sq. in. absolute and 70 F. and compresses it isothermally to 100 lbs. per sq. in. absolute, find (a) Pounds of air in cylinder at beginning of compression stroke. (b) The final volume of the compressed air. (c) The foot-pounds of work done upon the gas during compres- sion. (d) The B.t.u. absorbed by the air in increasing the internal energy, (c) The B.t.u. to be abstracted from the cylinder. 5. A cubic foot of air at a pressure of 150 lbs. per sq. in. gage expands isothermally until its pressure is 50 lbs per sq. in. gage. Calculate the work done during this expansion. PROBLEMS 39 6. Air at ioo lbs per sq. in. absolute and a volume of 2 cu. ft. expands along an» = 1 curve to 25 lbs. per sq. in. absolute pressure. Find (a) Work done by the expansion. (b) Heat to be supplied. 7. A quantity of air at 100 lbs. per sq. in. absolute pressure has a tem- perature of 8o° F. It expands isothermally to a pressure of 25 lbs. per sq. in. absolute when it has a volume of 4 cu. ft. Find (1) the mass of air present, (2) Work of the expansion in foot-pounds, (3) Heat required in B.t.u. 8. Air at 100 lbs. per sq. in. absolute pressure and 2 cu. ft. expands to 25 lbs. per sq. in. absolute adiabatically. What is the final volume? 9. One cubic foot of air at 6o° F. and a pressure of 15 lbs. per sq. in. absolute is compressed without loss or addition of heat to 100 lbs. per sq. in. absolute pressure. Find the final temperature and volume. 10. Two pounds of air are expanded from a temperature of 300 F. to 200 F. adiabatically. How many foot-pounds of work are developed? 11. A quantity of air having a volume of 1 cu. ft. at 6o° F. under a pres- sure of 100 lbs. per sq. in. absolute is expanded to 5 cu. ft. adiabatically^ Find the pounds of air present, the final temperature of the air and the work done during this expansion. 12. Data the same as in Problem 4 but the compression is to be adiabatic. Find (a) The final volume of the compressed air. (b) The final temperature of the compressed air. (c) The foot-pounds of work required to compress this air. (d) The B.t.u. absorbed by the air in increasing the internal energy. (e) The B.t.u. to be abstracted from the gas. 13. A pound of air at 32 F. and atmospheric pressure is compressed to 4 atmospheres (absolute). What will be the final volume and the work of compression if the compression is (a) isothermal, (b) adiabatic? 14. Plot the curve PV n = C, when n = 1.35. Initial pressure is 460 lbs. per sq. in. gage, initial volume 0.5 cu. ft., and final volume 8 cu. ft. 15. Prove that the work of an adiabatic expansion can be expressed by the formula: "—[-(in CHAPTER IV CYCLES OF HEAT ENGINES USING GAS The Heat Engine Cycle. In the heat engine, the working sub- stance or heat medium undergoes changes in its physical proper- ties converting heat into mechanical work. The series of such changes by the repetition of which the conversion of heat into work takes place forms the heat engine cycle.* The heat engine cycle usually consists of four events which are: heating, cooling, expansion, and compression. i. THE CARNOT CYCLE Very important conclusions regarding theoretically perfect heat engines are to be drawn from the consideration of the action of an ideal engine in which the working substance is a perfect gas which is made to go through a cycle of changes involving both isothermal and adiabatic expansions and compressions. This ideal cycle of operations was invented and first explained in 1824 by Carnot, a French engineer. This cycle gave the first theoretical basis for comparing heat engines with an ideally perfect engine. The ideal Carnot cycle requires an engine, illustrated in Fig. 7, which consists of the following parts: (1) A piston and cylinder, as shown in Fig. 7, composed of perfectly non-conducting material, except the cylinder-head (left- hand end of the cylinder) which is a good conductor of heat. The space in the cylinder between the piston and the cylinder head is occupied by the working substance, which can be assumed to be a perfect gas. * A thermodynamic machine performing a cycle in which heat is changed into work is called a heat engine, and one performing a cycle in which heat is trans- ferred from a medium at a low temperature to one at a higher temperature is called a refrigerating machine. 40 THE CARNOT CYCLE 41 (2) A hot body H of unlimited heat capacity, always kept at a temperature TV. (3) A perfectly non-conducting cover N. (4) A refrigerating or cold body R of unlimited heat receiving capacity, which is kept at a constant temperature T% (lower than Ti). H N Fig. 7. — Apparatus and Diagram Illustrating a Reversible (Carnot) Cycle. It is arranged that H, N or R can be applied, as required, to the cylinder head. Assume that there is a charge of one pound of gas in the cylinder between the piston and the cylinder head, which at the beginning of the cycle, with the piston in the posi- tion shown, is at the temperature T h has a volume V a , and has a pressure P a . The subscripts attached to the letters V and P refer to points on the pressure- volume diagram shown in Fig. 7. 42 CYCLES OF HEAT ENGINES USING GAS This diagram shows, by curves connecting the points a, b, c and d, the four steps in the cycle. The operation of this cycle will be described in four parts as follows: (i) Apply the hot body or heater H to the cylinder head at the left-hand side of the figure. The addition of heat to the gas will cause it to expand isothermally along the curve ab, because the temperature will be maintained constant during the process at T\. The pressure drops slightly to P b when the volume be- comes Vb. During this expansion external work has been done in advancing the piston and the heat equivalent of this work has been obtained from the hot body H. (2) Take away the hot body H and at the same time attach to the cylinder head the non-conducting cover N. During this time the piston has continued to advance toward the right, doing work without receiving any heat from an external source, so that the expansion of the gas in this step has been done at the expense of the stock of internal energy in the gas along the adiabatic curve be. The temperature has continued to drop in proportion to the loss of heat to the value T 2 . Pressure is then P c and the volume is V c . (3) Take away the non-conductor N and apply the refriger- ator R. Then force the piston back into the cylinder. The gas will be compressed isothermally at the temperature T 2 . In this compression, work is being done on the gas, and heat is developed, but all of it goes into the refrigerator R, in which the temperature is always maintained constant at T 2 . This com- pression is continued up to a point d in the diagram, so selected that a further compression (adiabatic) in the next (fourth) stage will cause the volume, pressure and temperature to reach their initial values as at the beginning of the cycle* (4) Take away the refrigerator R and apply the non-conduct- ing cover N. Then continue the compression of the gas without * Briefly the third stage of the cycle must be stopped when a point d is reached, so located that an adiabatic curve (PV 7 = constant) drawn from it will pass through the "initial" point a. THE CARNOT CYCLE 43 the addition of any heat. It will be the adiabatic curve da. The pressure and the temperature will rise and, if the point d has been properly selected, when the pressure has been brought back to its initial value P a the temperature will also have risen to its initial value 2\. The cycle is thus finished and the gas is ready for a repetition of the same series of processes comprising the cycle. To define the Carnot cycle completely we must determine how to locate algebraically the proper place to stop the third step (the location of d). During the second step (adiabatic ex- pansion from b to c) by applying equation (62), the following temperature and volume relations exist: Ti [Vol 7 - 1 T 2 lV b ] ' also for the adiabatic compression the fourth step can be sirni- lary stated, Hence, wr - wr Simplifying and transposing, we have V b V c v. v, < 68) V — is the ratio of expansion r for the isothermal expansion in V a the first step of the cycle. This has been shown (Equation 68) to be equal to — - in the isothermal compression in the third step in order that the adiabatic compression occurring in the fourth step shall complete the cycle. A summary of the heat changes to and from the working gas (per pound) in the four steps of the Carnot cycle is as fol- lows: 44 CYCLES OF HEAT ENGINES USING GAS (ab). Heat taken in from hot body (by equation (45), in foot-pounds) is: RTl\0g e ^- (69) • V a (be). No heat taken in or rejected. (cd). Heat rejected to refrigerator (by equation (45), in foot-pounds) is: V V * RT 2 log, — = - RT 2 log e -/• (70) V c V d (da). No heat taken in or rejected. Hence, the net amount of work done, W, by the gas in this cycle, being the mechanical equivalent (foot-pounds) of the excess of heat taken in over that rejected, is the algebraic sum of (69) and (70): W = r(t 1 log, y a -T, log, £) =R(T l - r 2 ) loge £• (71) The thermal or heat efficiency of a cycle is defined as the ratio of Heat equivalent of work done Heat taken in The heat equivalent of work done is, by equation (71), ic^-T^log,^, and the heat taken in is, by equation (69), The ratio above representing the efficiency E is: r (z\ - r 2 ) log. ^ E ^ = T -^- (72) RT, log, £ V a Log ---togpj. REVERSIBLE CYCLES 45 The efficiency of the Carnot cycle as expressed by equation (72) is the maximum possible theoretical efficiency which may be obtained with any heat engine working between the temperature limits 7\ and T 2 . This equation can be used as a standard for the comparison of the efficiencies of actual heat engines working between two temperature limits. Reversible Cycles. A heat engine which is capable of dis- charging to the "source of heat" when running in the reverse direction from that of its normal cycle the same quantity of heat that it would take from this source when it is running direct and doing work is said to operate with its cycle reversed, or, in other words, the engine is reversible. A reversible heat engine then is one which, if made to follow its indicator diagram in the reverse direction, will require the same horse power to drive it as a refrigerating machine as the engine will deliver when running direct, assuming that the quantity of heat used is the same in the two cases. An engine following Carnot's cycle is, for example, a reversible engine. The thermodynamic idea of reversibility in engines is of very great value because no heat engine can be more efficient than a reversible engine when both work between the same limits of temperature; that is, when both engines take in the same amount of heat at the same higher temperature and reject the same amount at the same lower temperature. It was first proved conclusively by Carnot that no other heat engine can be more efficient than a reversible engine when both work between the same temperature limits. To illustrate this principle, assume that there are two engines A and B. Of these let us say A is reversible and B is not. In their operation both take heat from a hot body or heater H and reject heat to a refrig- erator or cold body R. Let Q H be the quantity of heat which the reversible engine A takes in from the hot body H for each unit of work performed, and let Q B be the quantity of heat per unit of work which it discharges to the refrigerator R. For the purpose of' this discussion, assume that the non- reversible engine B is more efficient than the reversible engine A. 46 CYCLES OF HEAT ENGINES USING GAS Under these circumstances it is obvious that the engine B will take in less heat than A and it will reject correspondingly less heat to R per unit of work performed. The heat taken in by the non-reversible engine B from the hot body H we shall designate then by a quantity less than Q H , or Q H — X, and the heat rejected by B to the refrigerator R by Q R — X. Now if the non-reversible engine B is working direct (when converting heat into work) and is made to drive the reversible engine A according to its reverse cycle (when converting work into heat), then for every unit of work done by the engine B in driving the reversible engine A, the quantity of heat mentioned above, that is, Q H — X, would be taken from the hot body H by the non-reversible engine B and, similarly, the quantity of heat represented by Q H would be returned to the hot body H by the reverse action of the cycle of operations performed by A. This follows because the engine A is reversible and it returns, therefore, to H, when operating on the reverse cycle, the same amount of heat as it would take in from H when working on its direct cycle. By this arrangement the hot body H would be continually receiving heat, in the amount represented by X for each unit of work performed. At the same time the non-reversible engine B dis- charges to the refrigerator R a quantity of heat represented by Q R — X, while the reversible engine A removes from the refriger- ator R a quantity represented by Q R . As a result of this last operation the cold body will be losing continually per unit of work performed a quantity of heat equal to X. The combined per- formances of the two engines, one working direct as a normal heat engine and the other, according to its reverse cycle, as a com- pressor or what might be called a "heat pump/' gives a constant removal of heat from the refrigerator R to the hot body H, and as a result a degree of infinite coldness must be finally pro- duced in the refrigerator. If we assume that there is no mechanical friction, this com- bined machine, consisting of a normal heat engine and com- pressor, will require no power from outside the system. For this reason the assumption that the non-reversible engine B REVERSIBLE CYCLES 47 can be more efficient than the reversible engine A has brought us to a result which is impossible from the standpoint of expe- rience as embodied in the statement of the " Second Law of Thermodynamics "; that is, it is impossible to have a self-acting engine capable of transferring heat, infinite in quantity, from a cold body to a hot body. We should, therefore, conclude that no non-reversible engine, as B for example, can be more efficient than a reversible engine A when both engines operate between the same temperature limits. More briefly, when the source of heat and the cold receiver are the same for both a reversible heat engine and any other engine, then the reversible engine must have a higher possible efficiency; and if both engines are reversible it follows that neither can be more efficient than the other. A reversible engine is perfect from the viewpoint of efficiency; that is, its efficiency is the best obtainable. No other engine than a reversible engine which takes in and discharges heat at identical temperatures will transform into work a greater part of the heat which it takes in. Finally, it should be stated as regards this efficiency that the nature of the substance being expanded or compressed has absolutely no relation to the thermal efficiency as outlined above. If an engine operating on Carnot's cycle is reversed in its action, so that the same indicator diagram shown in Fig. 7 would be traced in the opposite direction, the reversed cycle, when begin- ning as before at point a with a perfect gas at the temperature Ti, will consist of the following stages: (1) When the non-conductor N is applied and the piston is advanced toward the right by the source of power performing the reversed cycle, the gas will expand, tracing the adiabatic curve ad, with constant lowering of temperature which at the point d will be T 2 . (2) When the non-conductor N is now removed, the refrig- erator R is applied, and the piston continues on its outward stroke. The gas will expand isothermally at the constant temperature T 2 , tracing the curve dc. During this stage the gas is taking heat from the refrigerator R. 48 CYCLES OF HEAT ENGINES USING GAS (3) When the refrigerator R is removed and the non-conductor N is again applied, which will be on the back stroke of the engine, the gas will be compressed, and on the indicator diagram another adiabatic curve cb will be traced. At the point b the temper- ature will be obviously T\. (4) When the non-conductor N is removed and the hot body H is again applied, with the compression continuing along the isothermal curve ba, heat will be discharged to the hot body H, while the temperature is maintained constant at 7\. The cycle has now been traced in a reverse direction from the beginning back to the starting point at a, and is now complete. During this process an amount of work represented by the area of the indicator diagram, equivalent in foot-pounds to R log e — - (7\ — T 2 ) (see equation 71), V a has been converted into heat. First, heat was taken from the refrigerator R, represented in amount by RT 2 logo ■=£■> V d and second, heat was rejected to the hot body H in the amount RTylog^ or -2?7\log3. As in direct operation of Carnot's cycle no heat is given or lost in the first and third stages outlined above. The algebraic sum of these two quantities, remembering that — = -=^- } gives the V a V d net amount of work done, W, on the gas, and, therefore, the net amount of heat (foot-pound units) transferred from the cold body R to the hot body H or, W = RT 2 log e ^ - RT, log, £ = -R log c £ (7\ - T 2 ). (73) V a y a y a HOT-AIR ENGINE CYCLES 49 Since the result is the same as given by equation (72), although opposite in sign on account of being work of compression, it will be observed that in the reverse cycle the same amount of heat is given to the hot body H as was taken from it in the direct operation of the same cycle, and that the same amount of heat is now taken from the refrigerator R as was in the other case given to it. 2. HOT-AIR ENGINE CYCLES The hot-air engine is a non-explosive type of external combus- tion heat engine, the working substance being atmospheric air which undergoes no change in its physical state. This type of prime-mover was invented about 100 years ago. It is little used on account of the difficulty in transmitting heat through the metallic walls to the dry gas air. Then the hot-air engine is very bulky in proportion to its power. There are also difficul- ties in carrying out practically the theoretical cycles of operation, on account of the rapid deterioration of the heat-conducting sur- faces. The mechanical efficiency of the hot-air engine is also low. The advantages of the hot-air engine are ease of operation and safety. Also its speed being low, on account of the rate of heat transmission, it is well suited for the driving of small pumps and for other domestic uses where small powers are required and also where the fuel-economy is a matter of minor importance. Hot-air engine cycles are divided into two groups : — Group I. External-combustion hot-air engines with a closed cycle and constant- volume temperature changes. Group II. External-combustion hot-air engines with an open cycle and constant-pressure temperature changes. In the hot-air engines an attempt was made to put in practice a cycle of the ideal Carnot type with the addition of a regenera- tor. The regenerator was a storage-battery of heat, its function being to absorb, store and return heat rapidly, replacing the adiabatic expansion curves of the Carnot cycle by lines of con- stant volume in group I and by lines of constant pressure in 5o CYCLES OF HEAT ENGINES USING GAS group II. The regenerator consists of a chamber containing strips of metal, coils of wire, or any other heat-absorbing material arranged in such a manner as to present a very large surface to the air passing through it. The Stirling Engine Cycle. The Stirling engine belongs to group I, the regenerator being so arranged that the pressure chops with the temperature at such a rate as to keep the vol- ume constant. It is an external-combustion engine and its I ) \> V*- N& ^&> ^ a v> X r 4„ d Volume Fig. 8. — Stirling Engine Cycle. cycle of operation is closed, the same air is used over and over again, any loss by leakage being supplied by a small force-pump. The engine consists, essentially, of a pair of dis- placer cylinders, a double-acting working cylinder, a regenera- tor and a refrigerator. In the earlier forms the displacer cyl- inder had a double wall, the regenerator and refrigerator being placed in the annular space surrounding the displacer cylinder. In the latter forms the regenerator and refrigerator are arranged separately from the displacer cylinder but in direct communi- cation with its top and bottom. A plunger works in the dis- placer cylinder, this plunger being filled with a non-conducting material such as brick-dust. The engine derives its heat by STIRLING ENGINE CYCLE 5 1 conduction from a furnace which is placed beneath the displac- ing cylinder. In the cycle represented by Fig. 8, the action of the engine is carried out as follows: 1. The substance, air, having a volume V a , a pressure P a and a temperature T a receives heat at constant volume by passing through the regenerator, and receives also heat from the furnace. As a result of the heat addition, its pressure is increased to P b , its temperature to T b , this process being represented by the constant volume line ab, Fig. 8. During this event the plunger is moving up. 2. The pressure under the working piston increases as a result of the addition of heat and the expansion of the air follows, producing the working stroke. This expansion is represented by be and is an isothermal, the air receiving heat from the furnace plates and the temperature remaining 7\. 3. The plunger descends, displacing the hot air and forcing the same through the regenerator and refrigerator. As a result of this, the temperature drops from T c to T& and the pressure is decreased from P c to P d , the volume remaining constant as shown by the line cd. 4. Due to this cooling effect the working piston descends com- pressing the air. This compression, represented by da, is iso- thermal, the air being cooled during the process by the regenera- tor and refrigerator to remain at the temperature TV Referring to Fig. 8 of the Stirling cycle, the useful work W is in foot-pounds, W = (jP b V b log, y>) - (p d V d log, y)' (H) The mean effective pressure is in pounds per square foot, M.E.P. = W ■ (75) V d — V a The horse power developed can be represented by H.P. = 5^- ( 7 6) 33,000 where N = revolutions (cycles) per minute. 52 CYCLES OF HEAT ENGINES USING GAS Since the expansion and compression processes are isothermal, the efficiency of the Stirling cycle is: P b V b log e ^-P d V d log ] E Vt V a P b V b log e Vc V b (77) Since V a = V b and V c = V d , also RTi = P b V b and RT 2 = PdV d , equation (77) becomes, E = RTr loge — c - RT^loge -=/ Vb V b Vc RT ± loge ^r Vb Tt -T 2 (78) The Ericsson Engine Cycle. This engine belongs to group II, the regenerator changing the temperature at constant pressure. This engine consists of five parts : a compressing pump, a receiver, a regenerator, a refrigerator and a working cylinder. The ideal a' 6 m CL, a b \Ti • NO* r ^ \Isothermal ^^sothermal • -r d Volume Fig. 9. — The Ericsson Engine Cycle. cycle for this engine is represented by Fig. 9, the order of events being as follows : Atmospheric air is drawn into the compressing pump as shown by d'd. This air is compressed isothermally to a, during the return stroke of the pump; it is then forced into a receiver as shown by aa! . Thus d'daa' represents the pump cycle. As the working cylinder begins its forward or up stroke, the THE LENOIR ENGINE 53 compressed air is admitted into the working cylinder at constant pressure. As this admission from a to b is through the regenera- tor, the entering air takes up heat increasing in temperature from Ti to T\. As soon as the supply of compressed air is cut off, the air expands isothermally along be to atmospheric pressure, while heat is being supplied by a furnace at the bottom of the working cylinder. During the return stroke of the working pis- ton, the air is discharged at constant pressure through the regen- erator, giving up its heat and is cooled to the temperature T 2 . In Fig. 9, a' bed' is the cycle of the working cylinder, the net work being represented by abed. The Ericsson cycle has the same efficiency as the Stirling cycle, the regenerator process being carried out at constant pressure instead of at constant volume. 3. INTERNAL-COMBUSTION ENGINE CYCLES The internal-combustion engine utilizes as its working sub- stance a mixture of air and gas or air and petroleum vapor. Combustion of the mixture takes place inside the engine cylinder, or in a communicating vessel, and the heat generated is converted into work. As the specific heat and the specific volume of the mixture do not differ much from that of air, the cyclical analy- sis and the theory of the internal-combustion engine are developed on the assumption that the working substance is air. The internal-combustion engine cycles can be divided into the follow- ing groups: Group I. Engines without compression. Group II. Compression engines. Group I. Internal-Combustion Engines Without Compression The Lenoir Engine. An engine of this group, invented by Pierre Lenoir in i860, was the first successful practical gas engine. The action of this type of engine is as follows : As the piston leaves the dead center it draws into the cylinder a charge of gas and air which is proportioned at the admission 54 CYCLES OF HEAT ENGINES USING GAS valve to form an explosive mixture. Admission is cut off some- what before half-stroke and this is followed by the ignition of the mixture by means of an electric spark. The explosion produces a rapid rise in pressure above atmospheric, thus forcing the piston to the end of the stroke. The exhaust valve opens near the end of the stroke and the burnt products are expelled during the return stroke of the piston. A fly-wheel carries the piston over during the exhaust stroke as well as also, during the suction stroke. The above series of operations takes place at each end of the piston, producing two impulses for each revolution. Fig. 10 represents the cycle of operations of the Lenoir engine Volume Fig. io. — Ideal Lenoir Cycle. on P-V coordinates. The drawing in of the mixture of gas and air at atmospheric pressure is represented by ab. Ignition takes place at b and is followed by the constant volume combustion line be. The working stroke, an adiabatic expansion, takes place to atmospheric pressure, as shown by cd, and the products of combustion are rejected during the return stroke of the piston da. Calling P, V, T the absolute pressure in pounds per square foot, the specific volume in cubic feet per pound of mixture, and the absolute temperature in degrees Fahrenheit respectively; also using subscripts b, c, d to designate the points at the corners bed of Fig. io, the following expressions will be obtained: THE LENOIR ENGINE 55 If the heat developed by the complete combustion of the mixture be designated by Q h then 6i = wC v (T c -T b ). (79) Since the combustion of the mixture takes place at constant volume, V c = V b T c = T b + 2*. (80) For unit weight, p. = p> £• (81) l 6 1 (82) The expansion cd being adiabatic (n = 7), If Q 2 is the heat rejected by the engine after performing its cycle of operations, Q 2 = wC v (T d - T b ). .(84) The useful work available is : W = J(Q 1 - Q 2 ). (85) The mean effective pressure is the average unbalanced pressure on the piston of the engine in pounds per unit area, and using symbols and units as on page 51, M.E.P. = ir i V- (S6) V d — V b The horse power developed would be found by equation h.p. = K2S2L, (87) 33,000 where N designates the number of explosions per minute. The cycle efficiency for the conditions of the problem is: 7? _ Qi ~ & ft _ T d — T b , RR x E -^or- I -Q 1 - t T zwr (88) 56 CYCLES OF HEAT ENGINES USING GAS Group II. Compression Engines The first compression engine was patented as early as 1799 by Philip Lebon. The thermodynamic advantages of compression before ignition will be evident from the demonstrations which follow. A mechanical advantage due to compression is the re- duced shock due to the explosion and the resulting improved, balance of parts. 1. The Otto Cycle. The Otto cycle, embodying the principles first proposed by Beau de Rochas in 1862, resulted in the most successful internal-combustion engine of to-day. This cycle was adopted by Dr. Otto in 1876, the operations being carried out in four consecutive equal strokes of the piston, requiring two com- plete revolutions of the engine crank-shaft. The ideal diagram Volume Fig. 11. — Otto Cycle. for the Otto cycle takes the form shown by Fig. 11, the operation being as follows: A mixture of gas and air is drawn in during the complete for- ward stroke of the piston, as shown by a' a. The return of the piston compresses the mixture along the adiabatic curve ab. Explosion of the compressed charge takes place at b, with the consequent combustion at constant volume to c. cd is the adia- THE BRAYTON CYCLE 57 batic expansion producing the second forward stroke. The ex- haust valve opens at d, cooling the gases to the exhaust pressure a, and rejecting them to the atmosphere. The heat added during the combustion from b to c is <2i = wC, (T c - T b ). (89) The heat rejected from d to a is ft = wC, (T d - T a ). (90) The cycle efficiency is E _ Qi-Q2 _ wC v {T c - T b ) -wC, {T d - T a ) _ Tg-Tg , . Qx wC v {T c -T b ) J T c -T b ' l9Ij Since the expansion and compression are adiabatic the follow- ing relations will hold: T a Va n - 1 = T b V b n ~\ and T c V c n - 1 = TaV^ 1 d Since V c = V b and V a = V d , d -L c . I J- d J- a J- a 7JT — 7fT> 2I S0 — — — — • J- a J- b -L c — J- & i&. Smce Tr(vj -Ur „ T a /VA"- 1 /PA"— i \ E = I -Tr I -{va) =i -{pJ n - (92) Equation (92) shows that the efficiency of the Otto cycle de- pends on the amount of compression before explosion. 2. The Brayton Cycle. This cycle is often called the Joule cycle after its inventor, or the Brayton cycle after George B. Brayton, who in 1872 designed an engine with gradual constant pressure combustion. In this engine a mixture of gas and air is first compressed in a separate pump and forced into a receiver. On the way from the receiver to the engine cylinder the mixture is ignited by a gas jet which burns steadily without sudden expkx sion, producing temperature and volume changes at constant pressure. After expansion the piston drives out the products of combustion at atmospheric pressure. The cycle of operations for the Brayton engine is represented 58 CYCLES OF HEAT ENGINES USING GAS by Fig. 12. a' a represents the supply of the combustible mixture to the pump where it is compressed adiabatically to b and forced into a receiver, be represents the burning of the compressed 6'- a'- b c - VAdiabatic \~~Adiabatic ^d a Volume Fig. 12. — Bray ton Cycle. mixture at constant pressure. As the mixture enters the working cylinder, it expands adiabatically along cd. This is followed by the rejection of the burnt gases along the atmospheric line da. The heat added during the constant pressure combustion from b to c is Qi = wC P (Tc - T b ). (93) The heat rejected from d to a is Q 2 = wC P (T d — T a ). (94) E The cycle efficiency is = Qi — Q2 = wCp (Tc — Tb) —wC p (Tg — Tg) _ Td — Tg , , Qi wC v (T c -Tb) _I T c -Tb {95) Since the expansion and compression phases of the cycle are adiabatic and P c = Pb\ Pa = Pa, therefore, Td _ Tc Tg Tb J- d -La -L a Tc-Tb ~ Y b " X and or =■-©" « Equation (96) is the same as equation (92) and shows that the cycle efficiencies of the Otto and Br ay ton cycles are the same, THE DIESEL CYCLE 59 under the same initial conditions, and depend on the amount of compression of the charge before explosion. 3. The Diesel Cycle. This cycle is carried out in four strokes of equal length, as in the case of the Otto cycle. Atmospheric air is drawn in during the complete forward stroke of the piston as shown by la (Fig. 13). The return of the piston compresses Fig. 13. — Diesel Engine Cycle. the air adiabatically to b, a pressure of about 500 pounds per square inch. At the end of the compression stroke a charge of the liquid fuel is injected in a finely divided form by an auxiliary pump or compressor and burns nearly at constant pressure when it comes in contact with the highly compressed air: The supply and combustion of the fuel, as represented by the combustion line be, is cut off at one-tenth to one-sixth the working stroke, depending upon the load. Expansion takes place during the balance of the stroke as shown by the adiabatic expansion line cd. Release occurs at d with the consequent drop in pressure, and the burnt gases are rejected during the fourth stroke of the cycle. The heat added (Qi) during the combustion of the fuel is: Q x = wC P (T c - T b ). (97) The heat rejected from d to a is Q 2 = wC v (T d - T a ). (98) The cycle efficiency is then, 60 CYCLES OF HEAT ENGINES USING GAS E „ ft -Q2 „ wC P (Tc. - T b ) - wC v (T d - T a ) Qi ' wC P (T c - T b ) C v (T d — T a \ I (T d — T a \ / x " X -C, Kf^Yj = '-yKf^Tj (99) PROBLEMS i. A Carnot engine containing 10 lbs. of air has at the beginning of the expansion stroke a volume of 10 cu. ft. and a pressure of 200 lbs. per sq. in. absolute. The exhaust temperature is o° F. If 10 B.t.u. of heat are added to the cycle, find (a) Efficiency of the cycle. (b) Work of the cycle. 2. A Carnot cycle has at the beginning of the expansion stroke a pressure of 75 lbs. per sq. in. absolute, a volume of 2 cu. ft. and a temperature of 200 F. The volume at the end of the isothermal expansion is 4 cu. ft. The exhaust temperature is $0° F. Find (a) Heat added to cycle. (b) Efficiency of cycle. (c) Work of cycle. 3. A cycle made up of two isothermal and two adiabatic curves has a pressure of 100 lbs. per sq. in. absolute and a volume of 1 cu. ft. at the begin- ning of the isothermal expansion. At the end of the adiabatic expansion the pressure is 10 lbs. per sq. in. absolute and the volume is 8 cu. ft. Find (a) Efficiency of cycle. (b) Heat added to cycle. (c) Net work of cycle. 4. In a Carnot cycle the heat is added at a temperature of 400 F. and rejected at 70 F. The working substance is 1 lb. of air which has a volume of 2 cu. ft. at the beginning and a volume of 4 cu. ft. at the end of the isothermal expansion. Find (a) Volume at end of isothermal compression. (b) Heat added to the cycle. (c) Heat rejected from cycle. (d) Net work of the cycle. 5. Air at a pressure of 100 lbs. per sq. in. absolute, having a volume of 1 cu. ft. and a temperature of 200 F., passes through the following opera- tions: 1st. Heat is supplied to the gas while expansion takes place under constant pressure until the volume equals 2 cu. ft. PROBLEMS 6l 2d. It then expands adiabatically to 15 lbs. per sq. in. absolute pressure. 3d. Heat is then rejected while compression takes place at con- stant pressure. 4th. The gas is then compressed adiabatically to its original volume of 1 cu. ft. Find (a) Pounds of air used. (b) Temperature at end of constant pressure expansion. (c) Heat added to the cycle. (d) Net work of cycle. (e) Efficiency of cycle. 6. A Stirling hot-air engine having a piston 16 inches in diameter and a stroke of 4 ft. makes 28 r.p.m. The upper temperature is 650 F., while the lower temperature is 150 F. Assuming that the volume of the working cylinder is one-half that of the displacer cylinder, calculate the pressures and volumes at each point of the cycle (Fig. 8) ; also calculate the mean effective pressure, the horse power developed, and the cycle efficiency. 7. Plot the Stirling engine cycle from the results of problem 6. 8. Compare the cycle efficiencies of internal-combustion engines working on the Otto cycle using the fuels and compression pressures as indicated below: Gasoline, 75; producer gas, 150; and blast furnace gas, 200 lbs. per sq. in. gage pressure. 9. Calculate the theoretical pressures, volumes and temperatures at each point of an Otto cycle, as well as the mean effective pressure, horse power, and cycle efficiency for the following conditions of Fig. 11. Assume that the pressure after compression is 180 lbs. per sq. in. gage, that 80 B.t.u. are added during combustion and that n in PV n = 1.4 : P a = 14.7 lbs. per sq. in., V a = 13.5 cu. ft., T a = 7° + 459-5 = 5 2 9-5° F. absolute. 10. Prove that cycle efficiency of the Diesel engine depends not only upon the compression pressure before ignition but also upon the point of cut-off C in Fig. 13. 11. In what respects do the actual cycles of internal-combustion engines differ from the theoretical Otto and Diesel cycles? 12. The demonstrations in the text for the various gas cycles were based on the assumption that the specific heats of gases are constant. Since the specific heats of gases vary at high temperatures, show the effect of this variability on the cyclic analysis. Refer to Lucke's Engineering Thermo- dynamics, Levin's Modern Gas Engines and the Gas Producer, and Clerk's Gas, Petrol and Oil Engines, Vol. II. CHAPTER V PROPERTIES OF VAPORS Saturated and Superheated Vapors. As was explained in the chapter on the properties of perfect gases, a vapor can be liqui- fied by pressure or temperature changes alone. At every pres- sure there is a fixed point, called the point of vaporization, at which a liquid can be changed into a vapor by the addition of heat. A vapor near the point of vaporization is called a saturated vapor and has a definite vaporization temperature for any given pressure. When a vapor is heated so that its temperature is greater than the vaporization temperature corresponding to a given pressure, it is said to be a superheated vapor. Superheated vapors only when far removed from the vaporization tempera- ture approach nearly the laws of perfect gases. Theory of Vaporization. When heat is added to a liquid its temperature will rise with a slight volume increase until the point of vaporization is reached. This is always a definite point for any given pressure and depends on the character of the liquid. Thus the point of vaporization of water at the atmospheric pres- sure of 14.7 pounds per square inch is 21 2 F., while that at a pres- sure of 150 pounds absolute is 358 F. On the other hand, the vaporization temperature of ammonia vapor at a pressure of 1 50 pounds absolute is 79 F. The increased temperature of vapori- zation with the pressure increase is due to the fact that the mole- cules being crowded, the velocity per molecule, or temperature, must be great enough to overcome not only molecular attraction but also external pressure before vaporization can take place. When the point of vaporization is reached, any further addition of heat will not cause any temperature increase, but internal work accompanied by vaporization will be produced as well as an enormous increase in volume. The heat required to entirely 62 VAPOR TABLES 63 vaporize a unit weight of a substance at a given pressure is termed the latent heat of vaporization. The volume developed when one unit weight of the liquid has been completely evaporated is called the specific volume of the dry vapor, this volume depending on the pressure. When vaporization is incomplete the vapor is termed a wet saturated vapor, which means that the vapor is in contact with the liquid from which it is formed. The percentage dryness in the vapor is called its quality. Thus the quality of steam is 0.97 when one pound of it consists of 97 per cent steam and 3 per cent water. While the volume of a vapor increases with the quality, the temperature is constant between the point of vaporization and the point of superheat for any given pressure. Thus the temperature of steam vapor corresponding to 150 pounds abso- lute is 358 F., no matter whether the quality is 0.10, 0.75 or 1.00. Further addition of heat after complete vaporization will cause temperature as well as volume changes, the substance being in the superheated vapor condition. Vapor Tables. The exact quantities of heat required to pro- duce the above effects under various conditions, as well as the 100 80 60 40 20 M = Marl 1 s and Da% is G = P = Good Peal) enou ody ffh M = 302.S G = 302.9 P = 302.95 ( ( M = h= 292.7 292.7 292.7 Ui^. <\ M = 267.3 G= 267.2 . P = 267.26 ( IM = 281.0 ' density pounds per cubic foot I- or -J, internal latent heat (p, i or I). In some tables will also be found a column for the total heat of vapor (H = q + r), external latent heat (APu) and entropy. Relation between Temperature, Pressure and Volume of Saturated Steam. The important relations of temperature, pres- sure and volume were first determined in a remarkable series of experiments conducted by a French engineer named Regnault, and it has been on the basis of his data, first published in 1847, that even our most modern steam tables were computed. Later experimenters have found, however, that these data were some- what in error, especially for values near the dry saturated condition. These errors resulted because it was difficult in the original apparatus to obtain steam entirely free from moisture. The pressure of saturated steam increases very rapidly as the temperature increases in the upper limits of the temperature scale. It is very interesting to examine a table of the properties of steam to observe how much more rapidly the pressure must be increased in the higher limits for a given range of temperature. It should be observed that in most tables the pressure is almost invariably given in terms of pounds per square inch, while in nearly ail our thermodynamic calculations the pressure must be used in pounds per square foot. The specific volume of saturated steam (v or s) is equal to the sum of the volumes of water (a) and of the increase in volume during vaporization («) , or V = a + U. (100) 66 PROPERTIES OF VAPORS Heat in the Liquid (Water) (h or q). The essentials of the process of making steam have been described in a general way. The relation of this process to the amount of heat required will now be explained. If a pound of water which is initially at some temperature t is heated at a constant pressure P (pounds per square foot) to the boiling point corresponding to this pres- sure and then converted into steam, heat will first be absorbed in raising the . temperature of the water from to to t, and then in producing vaporization. During the first stage, while the temperature is rising, the amount of heat taken in is approxi- mately (t — t ) heat units, that is, British thermal units (B.t.u.), because the specific heat of water is approximately unity and practically constant. This number of B.t.u. multiplied by 778 gives the equivalent number of foot-pounds of work. For the purpose of stating in steam tables the amount of heat required for this heating of water, the initial temperature t must be taken at some definite value; for convenience in numerical calculations and also because of long usage, the temperature 32 F. is invari- ably used as an arbitrary starting point for calculating the amount of heat " taken in." The symbol h (or sometimes i' or q) is used to designate the heat required to raise one pound of water from 32 F. to the temperature at which it is vaporized into steam. In other words, " the heat of the liquid" (h) is the amount of heat in B.t.u. required to raise one pound of water from 3 2 F. to the boiling point, or: h = \C dt. (101) C is the specific heat of water at constant pressure, U is the freezing point of water, / is the temperature to which the water is raised. As C is very nearly unity, the value of the heat absorbed by water in being raised to the steaming temperature (h) in B.t.u. can be expressed, approximately, by the formula h = t — 32 (in B.t.u.). (102) Values of h, taking into consideration the variation in the EXTERNAL WORK OF EVAPORATION 67 specific heat of water, will be found in the usual steam tables (Table 3). During this first stage, before any steaming has occurred, prac- tically all the heat applied is used to increase the stock of internal energy. The amount of external work done by the expansion of water as a liquid is practically negligible. Latent Heat of Evaporation (L or r). In the second stage of the formation of steam as described, the water at the temperature t, corresponding to the pressure, is changed into steam at that temperature. Although there is no rise in temperature, very much heat is nevertheless required to produce this evaporation or vaporization. The heat taken in during this stage is the latent heat of steam. In other words, the latent heat of steam may be defined as the amount of heat which is taken in by a pound of water while it is changed into steam at constant pres- sure, the water having been previously heated up to the tem- perature at which steam forms. The symbol L (also sometimes r) is used to designate this latent heat of steam. Its value varies with the particular pressure at which steaming occurs being somewhat smaller in value at high pressures than at low. The latent heat (L or r) of saturated steam can be approxi- mately calculated by the formula: L = 97O.4 — O.655 Q — 212) — O.OOO45 (t — 2T2) 2 . (103) External Work of Evaporation (Apu). A part of the heat taken in during the " steaming " process is spent in doing external work. Only a small part of the heat taken in is represented by the external work done in making the steam in the boiler, and the remainder of the latent heat (L) goes to increase the internal energy of the steam. The amount of heat that goes into the performing of external work is equal to P (the pressure in pounds per square foot) times the change of volume (u) occurring when the water is changed into steam, or Pu. Example. At the usual temperatures of the working fluid in steam engines the volume of a pound of water a is about sV of a cubic foot. The external work done in making one . pound of 68 PROPERTIES OF VAPORS steam having finally a volume of V (cubic feet) at a constant pres- sure P (pounds per square foot) may be written in foot-pounds: External work = Pu = P (V — -gV). C 1 ^) This last equation can be expressed in British thermal units (B.t.u.) by APu where A = yfg-. It is apparent also from this equation that the external work done in making steam is less at low pressure than at high,* because there is less resistance to over- come, or, in other words, P in equation (104) is less. The heat equivalent of the external work is, therefore, a smaller propor- tion of the heat added at low temperature than at high. Total Heat of Steam (H). The heat added during the process represented by the first and second stages in the formation of a pound of steam, as already described, is called the total heat of saturated steam or, for short, total heat of steam, and is repre- sented by the symbol H. Using the symbols already defined, we can write, per pound of steam, H = h + L (B.t.u.). (105) In other words, this total heat of steam is the amount of heat required to raise one pound of water from 32 F. to the tempera- ture of vaporization and to vaporize it into dry steam at that temperature under a constant pressure. Remembering that h for water is approximately equal to the temperature less 32 degrees corresponding to the pressure at which the steam is formed (t) the total heat of steam is approxi- mately, H = (t - 32) + L. (106) To illustrate the application of equation (106) calculate the total heat of steam being formed in a boiler at an absolute pres- sure of 1 1 5 pounds per square inch. * Although at the lower pressure the volume of a given weight of steam is greater than at a higher pressure, the change of pressure is relatively so much greater in the process of steam formation that the product of pressure and change of volume, P (V2 — Vi), which represents the external work done, is less for low pressure steam than for high. INTERNAL ENERGY OF EVAPORATION AND OF STEAM 69 From the steam tables (Table 3) the temperature t of the steam at a pressure of 115 pounds per square inch absolute is 338 F., the latent heat of vaporization is 880 B.t.u. per pound and the total heat of the steam is 1189 B.t.u. per pound. To check these values with equation (106), by substituting values of L and t, E = (338 - 3 2 ) + 880 = 1186 B.t.u. per pound. When steam is condensed under constant pressure, the process which was called the " second stage " is reversed and the amount of heat equal to the latent heat of evaporation (L) is given up during the change that occurs in the transformation from steam to water. Internal Energy of Evaporation and of Steam. It was ex- plained in a preceding paragraph that when steam is forming not all of the heat added goes into the internal or " intrinsic " energy of the steam, but that a part of it was spent in performing external work. If, then, the internal energy of evaporation is represented by the symbol I L , U-L-PZ-^. (107) This equation represents the increase in internal energy which takes place in the changing of a pound of water at the tem- perature t into steam at the same temperature. In all the formulas dealing with steam the state of water at 32 F. has been adopted as the arbitrary starting point from which the taking in of heat was calculated. This same arbitrary starting point is used also in expressing the amount of internal energy in the steam. This is the excess of the heat taken in over the external work done in the process. The total internal energy (L H ) of a pound of saturated steam at a pressure P in pounds per square foot is equal to the total heat (H) less the heat equivalent of the external work done; thus, i a = n-p {V ~/ t) - (108) 778 70 PROPERTIES OF VAPORS Such reference is made here to the internal energy of steam because it is very useful in calculating the heat taken in and rejected by steam during any stage of its expansion or com- pression. Heat taken in = increase of internal energy + external work done. When dealing with a compression instead of an expansion the last term above (external work) will be a negative value to indi- cate that work is done upon the steam instead of the steam doing work by expansion. The following problem shows the calculation of internal energy and external work: Example. A boiler is evaporating water into dry and satu- rated steam at a pressure of 300 pounds per square inch abso- lute. The feed Water enters the boiler at a temperature of 145 F. The internal energy of evaporation per pound of steam is I - l P ( V ~ ^ = Sn 3 °° X I44 ^' 551 ~ 7 ^ 778 " ' 6 778 - = 811.3 — 85.3 = 726.0 B.t.u., or taken directly from saturated steam tables equals 726.8 B.t.u. The total internal energy supplied above 32 F. per pound of steam is I H = H - P ( V ~ ^ = 1204.1 - 85.3 = 1118.8 B.t.u., or taken directly from saturated steam tables equals 11 18.5 B.t.u. External work done above 32 F. per pound of steam as calcu- lated from steam tables is H — I H = 1204.1 — 1118.5 = 85.6 B.t.u. External work of evaporation per pound of steam as calcu- lated from the steam tables is L -I L = 811.3 - 726.8 = 84.5 B.t.u. The external work done in raising the temperature of a pound of water from 32 F. to the boiling point is 85.6 - 84.5 = 1.1 B.t.u. WET STEAM 7 1 The external work done in raising the temperature of a pound of water from 3 2° F. to 145 F. is 300 X 144 (0.0163 — 0.01602) -p. £ ttfL ^ - = 0.01 B.t.u. 778 The external work done in forming the steam from water at 145 F. is, then, 84.5 + 1. 10 — 0.01 = 85.59 B.t.u. as compared with 85.3 B.t.u. as calculated from P (V ~ A) 778 It is to be noticed that the external work done during the addi- tion of heat when the liquid is raised to the vaporization tem- perature is small as compared with other values, and for most engineering work it is customary to assume that no external work is done during the addition of heat to the water. With this assumption I H = h + L- Piy ~ A) =H - (Z, - I L ). (109) 778 Steam Formed at Constant Volume. When saturated steam is made in a boiler at constant volume, as, for example, when the piping connections from the boiler to the engines are closed, then no external work is done, and all the heat taken in is converted into and appears as internal energy I H of the steam. This quantity is less than the total heat H of steam, representing its formation at constant pressure, by quantity P (V — ^V) -5- 778, where P represents the absolute pressure at which the steam is formed in pounds per square foot and V is the volume of a pound of steam at this pressure in cubic feet. Wet Steam. In all problems studied thus far, dealing with saturated steam, it has been assumed that the steaming process was complete and that the water had been completely converted into steam. In actual practice it is not at all unusual to have steam leaving boilers which is not perfectly and completely vapor- 72 PROPERTIES OF VAPORS ized; in other words, the boilers are supplying to the engines a mixture of steam and water. This mixture we call wet steam. It is steam which carries actually in suspension minute particles of water, which remain thus in suspension almost indefinitely. The temperature of wet steam is always the same as that of dry saturated steam as given in the steam tables, so long as any steam remains uncondensed. The ratio of the weight of moisture or water in a pound of wet steam to a pound of completely saturated steam is called the degree of wetness; and when this ratio is expressed as a per cent, it is called the percentage of moisture or " per cent wet." If in a pound of wet steam there is 0.04 pound of water in suspen- sion or entrained, the steam is four per cent wet. Another term, called the quality of steam, which is usually expressed by the symbol x, is also frequently used to represent the condition of wet steam. Quality of steam may be denned as the proportion of the amount of dry or completely evaporated steam in a pound of wet steam. To illustrate with the example above, if there is 0.04 pound of water in a pound of wet steam; the quality in this case would be 1 — 0.04 or 0.96. In this case the quality of this steam is ninety-six one-hundredths. With this understanding of the nature of wet steam it is obvi- ous that latent heat of a pound of wet steam is xL. Similarly, the total heat of a pound of wet steam is h + xL, and the volume of a pound of wet steam is x (V — ^V) + ih — xV + ^ (1 — x), or approximately it is equal to xV, because the term A (1 — x) is negligibly small except in cases where the steam is so wet as to consist mostly of water. Similarly, the internal energy in a pound of wet steam is Superheated Steam. When the temperature of steam is higher than that corresponding to saturation as taken from the steam tables, and is, therefore, higher than the standard temperature corresponding to the pressure, the steam is said to be super- THE TOTAL HEAT OF SUPERHEATED STEAM 73 heated. In this condition steam begins to depart and differ from its properties in the saturated condition, and when super- heated to a very high degree it begins to behave somewhat like a perfect gas. There are tables of the properties of superheated steam just as there are tables of saturated steam. (See Marks and Davis', Goodenough's or Peabody's Steam Tables.) When dealing with saturated steam there is always only one possible temperature and only one specific volume to be considered. With superheated steam, on the other hand, for a given pressure there may be any temperature above that of saturated steam, and corresponding to each temperature there will be, of course, definite values for specific volume and total heat. Like a perfect gas the specific volume or the cubic feet per pound increases with the increase in temperature. The total heat of superheated steam is obviously greater than the total heat of saturated steam.* Thus, since the total heat of dry saturated steam is, as before, h + L, the total heat of superheated steam with D degrees of superheat is Us = h + L + C p X D; (in) or if the temperature of the superheated steam is / sup . and / sa t. is the temperature of saturated steam corresponding to the pressure, H s = h + L + C p (4u P . — feat.). (112) H s (equations in and 112) is the total heat of superheated steam or is the amount of heat required to produce a pound of steam with the required degrees of superheat from water at 32 F. To obtain the amount of internal energy of a pound of steam (superheated) corresponding to this total heat as stated above, the external work expended in the steaming process must be subtracted; that is, * In practice steam is called dry saturated when it is exactly saturated and has no moisture. It is the condition known simply as saturated steam as regards the properties given in the ordinary steam tables. The dry saturated condition is the boundary between wet steam and superheated steam. 74 PROPERTIES OF VAPORS I H = h + L - P (F Sat - ~ A) + Cp (/ sup , - feaO - jP(7sUP ~ Fsat - ) 778 778 = ft -- 1; — Lsp \tsup. fsat.j r 7 778 ^ 0/ The term ^ can be neglected in the equations above for prac- tically all engineering calculations as the maximum error from this is not likely to be more than one in one thousand or xV per cent.* The accuracy of our steam tables for values of latent and total heat is not established to any greater degree. Making this approximation, the equation above becomes Ih = h -f- L -f- Cp (/sup. — /sat.) — ( • ) = H s '-' \ 778 / 778 If examination is made of the properties of superheated steam as given in Marks and Davis' or in Goodenough's Steam Tables for superheated steam at 165 pounds per square inch absolute pressure and 150 F. superheat, the following results are secured: Marks & Davis Goodenough Temperature (/) 516.0 516.1 Volume (7, v) 3.43 34i Total Heat (H, or h\ or i) 1277.6 1280.8 The values of h and L for saturated steam at this pressure are respectively 338.2 and 856.8. From the curves given, Fig. i7,{ * The error in the value of total internal energy due to neglecting the term -fa in the exercise worked out on page 70 is 0.85 B.t.u. per pound (one per cent of the external work), or an error of .076 per cent in the final result. f In their tables Marks and Davis represent the total heat of superheated steam by h. In this book the symbol Hs is used for greater clearness and to be consistent with the symbols used in the preceding formulas. They use also v for specific volume in place of V as above. J The curves for values of Cp, as given in Fig. 17, are for average and not for instantaneous values such as are given in Fig. 18, of Marks and Davis' Tables and Diagrams. Great caution must be observed in the use of curves of this kind. Those giving instantaneous values can only be used for the value of Cp in the form- ulas given for the total heat of superheated steam after the average value has been found by integrating the curve representing these values for a given pressure. DRYING OF STEAM BY THROTTLING OR WIRE-DRAWING 75 the specific heat of superheated steam at constant pressure (C p ) is 0.552. From these data, E s = h + L + C v X 150 = 338.2 + 856.8 + 0.552 X 150 = 1277.7. This value agrees very nearly with that given in the tables as previously indicated. .66 'J4 M .SO ■m * a J» "g oq .56 S | | 1 .54 Lb s. , Vbs - 227.2 " A 0, .52 3 ? "170.4 -142.2- -113.6 4! a ^0 - 85.2 » I - -5C.8 » 48 | 1 ■ — 28.4 ,, [ ■* - " .46 ,.44 ,.42 Fig. 17. 200 250 300 350 400 450 500 550 COO 650 700 750 Temperature ° P - Mean Values of Cp Calculated by Integration from Knoblauch and Jakob's Data. V = \ 0.5962 T—p (1+0.0014^) (- ■0.0833 |> (114) IP The specific volume (V) is calculated from the empirical form- ula derived from experimental results and is expressed as follows: '150 ,300,000 where p is in pounds per square inch, V is in cubic feet per pound and T = t + 460 is the absolute temperature on the Fahrenheit scale.* Drying of Steam by Throttling or Wire-drawing. When steam expands by passing through a very small opening, as, for example, * The value of 7 or ■=- of superheated steam used in ordinary engineering calculations is 1.3. 7 6 PROPERTIES OF VAPORS through a valve only partly open in a steam line, the pressure is considerably reduced. This effect is called throttling or wire- drawing. The result of expansion of this kind when the pressure O.90 ioo° 150 -200 250 o 300 temperature G. •350 Fig. i8. — Values of the "True" Specific Heat of Superheated Steam. is reduced and no work is done is that if the steam is initially wet it will be drier and if it is initially dry or superheated the degree of superheat will be increased. The reason for this is that the total heat required to form a pound of dry saturated steam (H) is considerably less at low pressure than at high, but obviously the total quantity of heat in a pound of steam must be THROTTLING OR SUPERHEATING CALORIMETERS 77 the same after wire- drawing as it was before, neglecting radiation. Now if steam is initially wet and the quality is represented by Xi, then the total heat in the steam is represented by fa plus XiLi, in which fa and Li represent the heat of the liquid and the latent heat of the steam at the initial pressure. If, also, the quality, heat of liquid and the latent heat of the steam after wire-drawing are represented respectively by X2, fa and Z2, then fa .+ X1L1 = fa + X2L2, or X1L1 + fa - fa . N X2= - (115) This drying action of steam in passing through a small open- ing or an orifice is very well illustrated by steam discharging from a small leak in a high pressure boiler into the atmosphere. It will be observed that no moisture is visible in the steam a few inches from the leak but farther off it becomes condensed by loss of heat, becomes clouded and plainly visible. An im- portant application of the throttling principle is also to be found in the throttling calorimeter (page 80). Determination of the Moisture in Steam. Unless the steam used in the power plant is superheated it is said to be either dry or wet, depending on whether or not it contains water in sus- pension. The general types of steam calorimeters used to de- termine the amount of moisture in the steam may be classified under three heads: 1 . Throttling or superheating calorimeters. 2. Separating calorimeters. 3. Condensing calorimeters. Throttling or Superheating Calorimeters. The type of steam calorimeter used most in engineering practice operates by passing a sample of the steam through a very small orifice, in which it is superheated by throttling. A very satisfactory calorimeter of this kind can be made of pipe fittings as illustrated in Fig. 19. It consists of an orifice O discharging into a chamber C, into which a thermometer T is inserted, and a mercury manometer 78 PROPERTIES OF VAPORS is usually attached to the cock V 3 for observing the pressure in the calorimeter. It is most important that all parts of calorimeters of this type, as well as the connections leading to the main steam pipe, should be very thoroughly lagged by a covering of good insu- lating material. One of the best materials for this use is hair felt, and it is particularly well suited for covering the more or less temporary pipe fittings, valves and nipples through which steam is brought to the calorimeter. Throttling calorimeters have been found useless because the small pipes leading to the calorimeters were not properly lagged, so that there was too much radiation, producing, of course, condensation, and the calorimeter did not get a true sample. It is obvious that if the entering steam contains too much moisture the drying action due to the throttling in the orifice may not be sufficient to super- heat. It may be stated in general that unless there are about 5° to io° F. of superheat in the calorimeter, or, in other words, unless the temperature on the low pressure side of the orifice is at least about 5 to io° F. higher than that corresponding to the pressure in the calorimeter, there may be some doubt as to the accuracy of results.* The working limits of throttling calo- rimeters vary with the initial pressure of the steam. For 35 pounds per square inch absolute pressure the calorimeter ceases to superheat when the percentage of moisture exceeds about 2 per cent; for 150 pounds absolute pressure when the moisture exceeds about 5 per cent; and for 250 pounds absolute pressure when it is in excess of about 7 per cent. For any given pressure the exact limit varies slightly, however, with the pressure in the calorimeter. * The same general statement may be made as regards determinations of superheat in engine and turbine tests. Experience has shown that tests made with from o to 10 degrees Fahrenheit superheat are not reliable, and that the steam consumption in many cases is not consistent when compared with results obtained with wet or more highly superheated steam. The errors mentioned when they occur are probably due to the fact that in steam, indicating less than 10 degrees Fahrenheit superheat, water in the liquid state may be taken up in "slugs" and carried along without being entirely evaporated. THROTTLING OR SUPERHEATING CALORIMETERS 79 In connection with a report on the standardizing of engine tests, the American Society of Mechanical Engineers * published instructions regarding the method to be used for obtaining a fair sample of the steam from the main pipes. It is recom- mended in this report that the calorimeter shall be con- nected with as short intermediate piping as possible with a so-called calorimeter nipple made of J-inch pipe and long enough to extend into the steam pipe to within | inch of the opposite wall. The end of this nipple is to be plugged so that the steam must enter through not less than twenty f-inch holes drilled around and along its length. None of these holes shall be less than J inch from the inner side of the steam pipe. The sample of steam should always be taken from a vertical pipe as near as possible to the engine, turbine or boiler being tested. A good example of a calorimeter nipple is illustrated in Fig. 20. The discharge valve V 2 should not be closed or adjusted without' first closing the gage cock V 3 . Unless this precaution is taken, the pressure may be suddenly increased in chamber C, so that if a manometer is used the mercury will be blown out of it; and if, on the other hand, a low-pressure steam gage is used it may be ruined by exposing it to a pressure much beyond its scale. Usually it is a safe rule to begin to take observations of tem- perature in calorimeters after the thermometer has indicated a maximum value and has again slightly receded from it. The quality or relative dryness of wet steam is easily calculated by the following method and symbols : pi = steam pressure in main, pounds per square inch absolute, p 2 = steam pressure in calorimeter, pounds per square inch absolute, t c = temperature in calorimeter, degrees Fahrenheit, L\ and hi = heat of vaporization and heat of liquid corre- sponding to pressure p h B.t.u., H 2 and t 2 = total heat (B.t.u.) and temperature (degrees Fahrenheit) corresponding to pressure p 2 , * Proceedings American Society of Mechanical Engineers, vol. XXI. 8o PROPERTIES OF VAPORS Op specific heat of superheated steam. Assume 0.47 for low pressures existing in calorimeters, initial quality of steam. Connection for Manometer Fig. 19. — Simple Throttling Steam Calorimeter. Total heat in a pound of wet steam flowing into orifice is XiU + h h and after expansion, assuming all the moisture is evaporated, the total heat of the same weight of steam is H 2 ~r Lp \pc — W). Then assuming no heat losses and putting for C p its value 0.47 : X1L1 + h = H 2 + 0.47 (t e — t 2 ) (116) H 2 + 0.47 (t c — t 2 ) — hi Xi = JU (117) BARRUS, THROTTLING CALORIMETER 8l The following example shows the calculations for finding the quality of steam from the observations taken with a throttling calorimeter : Example. Steam at a pressure of ioo pounds per square inch absolute passes through a throttling calorimeter. In the calo- rimeter the temperature of the steam becomes 243 ° F. and the pressure 15 pounds per square inch absolute. Find the quality. Solution. By taking values directly from tables of properties of superheated steam,* the total heat of the steam in the calorim- eter at 15 pounds per square inch absolute pressure and 243 ° F. is 1 164.8 B.t.u. per pound or can be calculated as follows: E + C v {t c - t 2 ) = 1150.7 + 0.47 ( 2 43 - 2I 3) = 1 164.8 B.t.u. per pound. (Note. t c = temperature in calorimeter and t 2 = temperature corresponding to calorimeter pressure.) The total heat of the steam before entering the calorimeter is h + xL. At 100 pounds per square inch absolute pressure, this is 298.3 + 888.0 x in B.t.u. per pound. Since the heat in the steam per pound in the calorimeter is obviously the same as before it entered the instrument, we can equate as follows: 298.3 + 888.0 x = 1164.8 x = 0.976 or the steam is 2.4 per cent wet. Barrus Throttling Calorimeter. This is an important varia- tion from the type of throttling calorimeter shown in Fig. 19 and has been quite widely introduced by Mr. George H. Barrus. In this apparatus the temperature of the steam admitted to the calorimeter is observed instead of the pressure and a very free exhaust is provided so that the pressure in the calorimeter is atmospheric. This arrangement simplifies very much the obser- vations to be taken, as the quality of the steam X\ can be calcu- lated by equation (117) by observing only the two temperatures * Marks and Davis' Steam Tables and Diagrams (1st ed.), page 24 or Goodenough's Properties of Steam and Ammonia (2d ed.), page 47. 82 PROPERTIES OF VAPORS Fig. 20. Barms' Throttling Steam Calorimeter. /1 and t c , taken respectively on the high and low pressure sides of the orifice in the calorimeter. This calorimeter is illustrated in Fig. 20. The two thermometers required are shown in the figure. Arrows indicate the path of the steam.* The orifice in such calorimeters is usually made about ft- inch in diameter, and for this size of orifice the weight of steam | discharged per hour at 175 pounds per square inch absolute pressure is about 60 pounds. It is impor- tant that the orifice should always be kept clean, because if it be- comes obstructed there will be a reduced quantity of steam passing through the instrument, making the error due to radiation rela- tively more important. In order to free the orifice from dirt or other obstructions the connecting pipe to be used for attaching the calorimeter to the main steam pipe should be blown out thoroughly with steam before the calorimeter is put in place. The connecting pipe and valve should be covered with hair felting not less than f inch thick. It is desirable also that there should be no leak at any point about the apparatus, as in the stuffing-box of the supply valve, the pipe joints or the union. With the help of a diagramf giving the quality of steam directly the Barrus calorimeter is particularly well suited for use in power plants, where the quality of the steam is entered regu- larly on the log sheets. The percentage of moisture is obtained immediately from two observations without any calculations. Separating Calorimeters. It was explained that throttling calorimeters cannot be used for the determination of the quality of steam when for comparatively low pressures the moisture * Transactions of American Society of Mechanical Engineers, vol. XI, page 790. f In boiler tests corrections should be made for the steam discharged from the steam calorimeters. J See page 113, and also Moyer's Power Plant Testing, (2d ed.), pages 58-60. SEPARATING CALORIMETERS 83 -z = Steam Water is in excess of 2 per cent, and when for boiler pressures commonly used it exceeds 5 per cent. For higher percentages of moisture than these low limits separating calorimeters are most generally used. In these instruments the water is removed from the sample of steam by mechanical separation just as it is done in the ordinary steam separator installed in the steam mains of a power plant. There is pro- vided, of 'course, a device for de- termining, while the calorimeter is in operation, usually by means of a calibrated gage glass, the amount of moisture collected. This me- chanical separation depends for its action on changing very abruptly the direction of flow and reducing the velocity of the wet steam. Then, since the moisture (water) is nearly 300 times as heavy as steam at the usual pressures de- livered to the engine, the moisture will be deposited because of its greater inertia. Fig. 21 illustrates a form of sep- arating calorimeter having a steam jacketing spaqe which receives live steam at the same temperature as the sample. Steam is supplied through a pipe A, discharging into a cup B. Here the direction of the flow is changed through nearly 180 degrees, causing the moisture to be thrown outward through the meshes in the cup into the vessel V. The dry steam passes upward through the spaces between the webs W, into the top of the outside jacketing chamber J, and is finally discharged from the bottom of this steam jacket through the nozzle N. This nozzle is consider- ably smaller than any other section through which the steam flows, so that there is no appreciable difference between the pres- sures in the calorimeter proper and the jacket. The scale Fig. 21. — Separating Calorimeter. 84 PROPERTIES OF VAPORS opposite the gage glass G is graduated to show, in hundredths of a pound, at the temperature corresponding to steam at ordinary working pressures, the variation of the level of the water accumulating. A steam pressure gage P indicates the pressure in the jacket J, and since the flow of steam through the nozzle N is roughly proportional to the pressure, another scale in addition to the one reading pressures is provided at the outer edge of the dial. A petcock C is used for draining the water from the instrument, and by weighing the water col- lected corresponding to a given difference in the level in the gage G the graduated scale can be readily calibrated. Too much reliance should not be placed on the readings for the flow of steam as indicated by the gage P unless it is frequently calibrated. Usually it is very little trouble to connect a tube to the nozzle N and condense the steam discharged in a large pail nearly filled with water. When a test for quality is to be made by this method the pail nearly filled with cold water is carefully weighed, and then at the moment when the level of the water in the water gage G has been observed the tube attached to the nozzle N is immedi- ately placed under the surface of the water in the pail. The test should be stopped before the water gets so hot that some weight is lost by " steaming." The gage P is generally cali- brated to read pounds of steam flowing in ten minutes. For the best accuracy it is desirable to use a pail with a tightly fitting cover into which a hole just the size of the tube has been cut. If W is the weight of dry steam flowing through the orifice N and w is the weight of moisture separated, the quality of the steam is W + w Condensing or Barrel Calorimeter. For steam having a large percentage of moisture (over 5 per cent) the condensing or barrel calorimeter will give fairly good results if properly used. In its simplest form it consists of a barrel placed on a platform scale and containing a known weight of cold water. The steam is introduced by a pipe reaching nearly to the bottom of the EQUIVALENT EVAPORATION AND FACTOR OF EVAPORATION 85 barrel. The condensation of the steam raises the temperature of the water, the loss of heat by the wet steam being equal to the gain of heat by the cold water. It will, therefore, be neces- sary to observe the initial and final weights, the initial and final temperatures of the water in the barrel and the temperature of the steam. Let W = original weight of cold water, pounds. w = weight of wet steam introduced, pounds. tx — temperature of cold water, degrees Fahrenheit. t 2 = temperature of water after introducing steam. t s = temperature of steam. L = latent heat of steam at temperature t s . x = quality of steam. Then, Heat lost by wet steam = heat gained by water. wxL + w (t s — h) = W (t 2 — h) X = wl (lI9) The accuracy of the results depends obviously upon the accu- racy of the observation, upon thorough stirring of the water so that a uniform temperature is obtained and upon the length of time required. The time should be just long enough to obtain accurate differences in weights and temperatures; otherwise, losses by radiation will make the results much too low. Equivalent Evaporation and Factor of Evaporation. For the comparison of the total amounts of heat used for generating steam (saturated or superheated) under unlike conditions it. is necessary to take into account the temperature t Q at which the water is put into the boiler as well as also the pressure P at which the steam is formed.* These data are of much impor- tance in comparing the results of steam boiler tests. The basis * As the pressure P increases the total heat of the steam also increases; but as the initial temperature of the water ("feed temperature") increases the value of the heat of the liquid decreases. 86 PROPERTIES OF VAPORS of this comparison is the condition of water initially at the boil- ing point for "atmospheric" pressure or at 14.7 pounds per square inch; that is, at 212 F. and with steaming taking place at the same temperature. For this standard condition, then, h = o and H = L = 970.4 B.t.u. per pound. Evaporation under these conditions is described as, " from (a feed-water temperature of) and at (a pressure corre- sponding to the temperature of) 212 F." To illustrate the application of a comparison with this stand- ard condition, let it be required to compare it with the amount of heat required to generate steam at a pressure of 200 pounds per square inch absolute with the temperature of the water sup- plied (feed water) at 190 F. For P = 200 pounds per square inch absolute the heat of the liquid h = 354.9 B.t.u. per pound and the heat of evaporation (L) is 843.2 B.t.u. per pound. For t = 190 F. the heat of the liquid (ho) is 157.9 B.t.u. per pound. The total heat actually required in generating steam at these conditions is, therefore, 843.2 + (354.9 — I57-9) = 1040-2 B.t.u. per pound. The ratio of the total heat actually used for evaporation to that necessary for the condition defined by " from and at 212 F." is called the factor of evaporation. In this case it is the value 1040.2 t- 970.4 = 1.07. Calling F the factor of evaporation, h and L respectively the heats of the liquid and of evaporation corresponding to the steam pressure and h Q the heat of the liquid corresponding to the tem- perature of feed water, then ^ = L + (h-ho) . (i2q) 970.4 The actual evaporation of a boiler (expressed usually in pounds of steam per hour) multiplied by the factor of evaporation is called the equivalent evaporation. PROBLEMS 87 Vapors as Refrigerating Media. Ammonia is generally used as the refrigerating medium in connection with mechanical refrigeration. Carbon dioxide and sulphur dioxide are also used to a limited extent as refrigerating media. The value of a substance as a refrigerating medium depends upon its latent heat, its vaporization temperature, its cost, and upon its chemical properties. The greater the latent heat of a refrigerating medium the more heat will it be capable of abstract- ing by evaporation. Upon the vaporization temperature of the refrigerant at different pressures depends the degree of cold it can produce as well as its practicability for use in hot climates where low temperature cooling water cannot be secured. Goodenough's Tables of Properties of Steam and Ammonia give the various physical properties of saturated, superheated and liquid ammonia. Peabody's Tables give the properties of ammonia, sulphur dioxide, carbon dioxide and of other vapors used as refrigerating media. Table 4 is an abridged table based upon Goodenough's values for saturated ammonia. Tables 5 and 6, based upon Peabody's Tables, show some of the properties of sulphur dioxide (S0 2 ) and of carbon dioxide (C0 2 ). PROBLEMS 1. Dry and saturated steam has a pressure of 100 lbs. per sq. in. absolute. Calculate the temperature of the steam, the volume per pound, the heat of the liquid, the latent heat, and the total heat above 32 F. per pound of this steam. 2. Dry and saturated steam has a temperature of 300 F. What is its pressure, heat of the liquid, latent heat, and total heat? 3. A closed tank contains 9 cu. ft. of dry and saturated steam at a pressure of 150 lbs. per sq. in. absolute. (a) What is its temperature? (b) How many pounds of steam does the tank contain? 4. A boiler generates dry and saturated steam under a pressure of 200 lbs. per sq. in. absolute. The feed water enters the boiler at 6o° F. (a) What is the temperature of the steam? (b) How many British thermal units are required to generate 1 lb. of this steam if this feed water is admitted at 32 F.? 88 PROPERTIES OF VAPORS (c) How many British thermal units are required to generate i lb. of this steam from feed water at 60 ° F. into the steam at the pressure stated at the beginning of this prob- lem? 5. One pound of dry and saturated steam is at a pressure of 250 lbs. per sq. in. absolute. (a) What is its internal energy of evaporation? (b) What is its total internal energy above 32 F.? (c) How much external work was done during its formation from 32° F.? (d) How much external work was done during the evaporation? (e) How much external work was done during the change in temperature of the water from 32 degrees to the boiling point corresponding to the pressure? 6. Dry and saturated steam is generated in a boiler and has a tempera- ture of 400 F. The feed water enters the boiler at 200 F. (a) What pressure is carried in the boiler? (b) What is the total heat supplied to generate 1 lb. of this steam? (c) How much external work was done during its formation? (d) How much heat was used in increasing the internal energy? Check this by (hi — hi + II) noting that this assumes no external work done in the heating of the liquid. 7. One pound of steam at a pressure of 100 lbs. per sq. in. absolute has a quality of 90 per cent dry. What is its temperature? 8. How many British thermal units would be required to raise the pound of steam in the above problem from 32 F. to the boiling point corre- sponding to the pressure stated? 9. What would be the volume of a pound of steam for the conditions stated in problem 7? 10. How many heat units (latent heat) are required to evaporate the steam in problem 7? 11. What is the amount of the total heat (above 32 F.) of the steam in problem 7? 12. What would be the external work of evaporation of the steam in problem 7? 13. How much external work (above 32 F.) is done in making steam as in problem 7? 14. What is the internal energy of evaporation of the steam in problem 7? 15. What is the total internal energy of the steam in problem 7? 16. A tank contains 9 cu. ft. of steam at 100 lbs. per sq. in. absolute pressure which has a quality of 0.95. How many pounds of steam does the tank contain? PROBLEMS 89 17. Two pounds of steam have a volume of 8 cu. ft. at a pressure of 100 lbs. per sq. in. absolute. What is the quality? Calculate its total heat above 32 F. 18. One pound of steam having a quality of 0.95 has a temperature of 3 2 5 F. What is the pressure? 19. One pound of steam at a pressure of 225 lbs. per sq. in. absolute has a temperature of 441. 9 F. (a) Is it superheated or saturated? (b) What is the total heat required to generate such steam from water at 32 F.? (c) What is its volume? (d) How much external work was done (above 32 F.) in generat- ing it? (e) How much internal energy above 32 F. does it contain? 20. One pound of steam at a pressure of 300 lbs. per sq. in. absolute has a volume of 1.80 cu. ft. (a) Is it saturated or superheated? (b) What is its temperature? (c) How much is its total heat above 32 F.? (d) What is its total internal energy? 21. Steam in a steam pipe has pressure of 110.3 lbs. per sq. in. by the gage. A thermometer in the steam registers 385 F. Atmospheric pres- sure is 14 lbs. per sq. in. absolute. Is the steam superheated, and if superheated how many degrees? 22. Steam at a pressure of 200 lbs. per sq. in. absolute passes through a throttling calorimeter.. After expansion into the calorimeter the tem- perature of this steam is 250 F. and the pressure 15 lbs. per sq. in. abso- lute. What is the quality? 23. Steam at a temperature of 325 F. passes through a throttling calorimeter. In the calorimeter the steam has a pressure of 16 lbs. per sq. in. absolute and a temperature of 236. 3 F. What is the quality? 24. Steam at 150 lbs. per sq. in. absolute pressure passes through a throttling calorimeter. Assuming that the lowest condition in the calorim- eter for measuring the quality is io° F. superheat and the pressure in the calorimeter is 15 lbs. per sq. in. absolute, what is the largest percentage of wetness the calorimeter is capable of measuring under the above conditions? 25. Prepare a chart by means of which can be determined the largest percentages of wetness a throttling calorimeter will measure at all pressures from 50 to 300 lbs. per sq. in. absolute. 26. In a ten-minute test of a separating calorimeter the quantity of dry steam passing through the orifice was 9 pounds. The quantity of water separated was 1 pound. What was the quality? 90 PROPERTIES OF VAPORS 27. A barrel contained 400 lbs. of water at a temperature of 50 F. Into this water steam at a pressure of 125 lbs. per sq. in. absolute was admitted until the temperature of the water and condensed steam in the barrel reached a temperature of ioo° F. The weight of the water in the barrel was then 418.5 lbs. What was the quality? 28. Calculate the factor of evaporation and the equivalent evaporation per pound of coal for a boiler under the following conditions: Steam pres- sure, 190 lbs. per sq. in. gage; feed water temperature, 203 F.; steam appar- ently evaporated per pound of coal i\ pounds; steam 3 per cent wet. 29. Plot on one chart the pressure-temperature relations of ammonia, SO2, and CO2. 30. Plot on one chart the pressure-latent heat relations of ammonia, SO2, and CO2. 31. What conclusions do you reach from the graphic results in problems 29 and 30? 32. If cooling water for condensing ammonia cannot be secured at a tem- perature less than 90 F., what will be the pressure of the ammonia at the inlet to the condenser of the refrigerating system? CHAPTER VI t I ■3 w SQ / dQ T .i Entropy- 4> - Analysis of Entropy Diagram. • ENTROPY Pressure-volume diagrams are useful for determining the work (in foot-pounds), done during any process or a cycle, but they are of very limited use in analyz- ing the heat changes involved. It has, therefore, been found desirable to make use of a diagram which shows directly by an area the number of heat units (instead of foot-pounds) in- volved during any process. In order that an area shall represent this value the coordinates must be such that their product will give heat units. If the ordinates are in absolute temperature, Fig. 22. the abscissas must be heat units per degree of absolute temperature, that is, -^> for then T X^ = Q, the amount of heat added during the process. Suppose that the heat Q, which is required to produce a process, such as an expansion or a compression, is divided up into a number of small increments dQ (Fig. 22) and that each small increment of heat is divided by the average absolute temperature at which the heat change occurs. There will then be a series of expressions -^ which, when integrated, will give the total change in the abscissas. This quantity I -^ when multiplied by the average absolute temperature between C and D will give the total amount of heat involved during the process. Mathematically expressed, the change in the abscissas is dQ T - v T or = f (121) 92 ENTROPY The heat change involved is dQ = Td or Q = Ct d. (122) The quantity in the equations is known as the increase in en- tropy of the substance, and may be denned as a quantity which, when multiplied by the average absolute temperature occurring during a process, will give the number of heat units (in B.t.u.) added or abstracted as heat during the process. The " increase in entropy" is employed rather than entropy itself, because only the differences in entropy are important. This definition of entropy states that in a temperature-entropy diagram such as Fig. 22, where the ordinates are absolute tem- peratures, and the abscissas are entropies as calculated above some standard temperature, the area under any line CD gives the number of heat units added to the substance in passing from a temperature T\ and entropy <£i = Oe to a temperature T 2 and entropy <£ 2 = Of (or the number of heat units abstracted in pass- ing from T 2 to 7\) . Entropy Changes During Constant Pressure Expansions of Gases. The heat supplied or abstracted during a constant pressure expansion or compression of a gas may be stated: dQ = wCpdt, (123) or (^ = wC p (r 2 — Ti). (124) From equation (121) the change in entropy is Assuming the specific heat C v constant, the change in entropy becomes : r T *dt = wCp J - (126) = WC P (loge T 2 — l0g e Ti) = wC P \og e7 ^- (127) I 1 ENTROPY CHANGES 93 Entropy Changes of Gases at Constant Volume. The heat supplied or abstracted during a constant volume change of a gas may be stated: dQ = wCvdt, (128) or Q = wC v (T 2 — Ti). (129) Assuming, as before, the specific heat under constant volume (C v ) constant and substituting in equation (121), the change in entropy is = wC v J - (130) = WCv (l0g e T 2 - lOge Ti) (131) = wC v log e7 ^' (132) 1 1 Entropy Changes During Isothermal Processes of a Gas. During an isothermal change the temperature remains constant. The heat supplied or abstracted is consequently equal to the heat equivalent of the work done, which in terms of weight and temperature is wRTloge-^ ? - (133) Vl Since the temperature remains constant, the change in entropy is = «* ri °*£; (134) = WR \0g e ^. (135) V 1 Entropy Changes During Reversible Adiabatic Processes of Gases. The heat supplied to or abstracted from an adiabatic expansion or compression is, by definition, zero. The entropy change in such a process is *=r?=°- (i36) Hence during an adiabatic process no change of entropy occurs. "7 d - s T X A B H - T 2 D c (V ■»-> 3 f-H o OQ .Q e / 94 ENTROPY It is possible for adiabatic processes to occur which are not reversible. These are processes in which, not only no heat is added or abstracted, but a portion or all the work of the process may reappear in the working medium as heat. In such a process the entropy does not remain constant. Reversible adiabatic processes are sometimes called isoentropic (equal entropy) to distinguish them from the irreversible adiabatic processes.^ Entropy Changes During a Carnot Cycle. A pound of the working substance is first expanded isothermally. On a T-cj> (temperature-entropy) diagram (Fig. 23), this process would be represented by line AB, where the temperature re- mains constant at T\, and where the entropy increases from Oe to Of, be- cause of the addition of heat that is re- Entropy-0 quired to keep the temperature constant. Fig. 23. — Entropy Diagram The next process is adiabatic expan- of Carnot Cycle. • r t> 4. 't tt ^ • *i_i 3 sion from ii to 1 2 - Heat is neither added to nor abstracted from the substance during this expan- sion. Hence the entropy remains constant, as indicated by BC. The substance is now isothermally compressed along CD, the temperature remaining constant at T 2 and the entropy decreasing because of the abstraction of heat. The last process of the cycle is the adiabatic compression from D to A, no heat being added or abstracted, and the entropy, therefore, remaining constant. The heat supplied during the cycle is represented by the area, ABfe and equals ($f - 4>e) Tl (137) The heat abstracted during the cycle is represented by the area, CDef, and equals (0/ - e ) T 2 . (138) Since the work of the cycle, in terms of heat, equals the heat added minus the heat rejected, TEMPERATURE-ENTROPY DIAGRAMS FOR STEAM 95 Work = Area ABfe — area CDef = Area ABCD. In terms of entropy, Work = (/ — e ) Ti — (/ — 4> e ) T 2 = (7\ - T 2 ) (0/ - e ). (139) Efficiency of cycle is, „ Area ABCD E = Area ABfe (7\ - - T 2 ) (0/ - 4>c) = T, - T 2 T\ (0/ — 0e) 2\ (140) From the foregoing discussion two important conclusions may be drawn in regard to the use of the T-<$> diagram : 1. If any heat process be represented by a curve on a T- diagram, the heat involved during the process is equal to the area under the curve, that is, between the curve and the axis of absolute temperature. 2. If a cycle of heat processes be represented on a T-0 diagram by a closed figure, the net work done is equal to the enclosed area, that is, the enclosed area measures the amount of heat that was converted into work. T-0 diagrams are useful for analyzing heat processes, and find particularly useful application in steam engineering, as indicated by the following: 1. Graphical analysis of heat transfers in a steam engine cylinder. 2. Determination of quality of steam during adiabatic ex- pansion. 3. Calculations of steam engine cycle efficiencies. 4. Steam turbine calculations. Temperature-Entropy Diagrams for Steam. A temperature- entropy diagram for steam is shown in Fig. 24. The various shaded areas represent the heats added to water at 32 F. to completely vaporize it at the pressure Pi. The area ABCD is the heat added to the water to bring it to the temperature of vaporization, or represents the heat of the liquid (h) for the pres- 9 6 ENTROPY sure P\. Further heating produces evaporation at the constant temperature T\ corresponding to the pressure Pi, and is repre- sented by the area under the line CE. When vaporization is complete, the latent heat, or the heat of vaporization (Z), is the area DCEF. If, after all the water is vaporized, more heat is added, the steam becomes superheated, and the additional heat required would be represented by an area to the right of E. Dry Steam or Saturation Line 1.5 2.0 0.5 1.0 Entropy (0) Fig. 24. — Temperature-entropy Diagram of Steam. Calculation of Entropy for Steam. In order to lay off the increase in entropy as abscissas in the heat diagram for steam, it is necessary to determine various values. For convenience 3 2 F. has been adopted as the arbitrary starting point for cal- culating increase of entropy, as well as for the other thermal properties of steam. Referring to Fig. 25 the entropy of water is seen to be o at 32 F. In order to raise the temperature from To to Ti, h heat units are required, and by the equation (121), the entropy of one pound of the liquid 6 will be C Tl dh ( , = / -57> 04i) To T or, assuming the specific heat of water to be unity we can write T = l0ge T X - l0g e To = l0g e —-- 1 (142) CALCULATION OF ENTROPY FOR STEAM 97 In order to evaporate the water into steam at the boiling point Tij the latent heat, L, must be added at constant temperature 7\. The increase of entropy during the "steaming" process is represented by — and is equal to, in this case, Ora. Eahr. 328+788 (143) k ft Entropy- logr e T 2 — H log e Tx- Fig. 25. — Diagram for Calculation of Entropy of Steam. Further heating would produce superheated steam and the change in entropy would be Entropy of superheat = / = C p log rsu p- Cpdt Ts&t. * ' T J- sup. sat. (144) (145) where C P = specific heat of the superheated steam at constant pressure. T S uv. = absolute temperature of the superheated steam. Ts*t. = absolute temperature of the saturated steam. 98 * ENTROPY Total Entropy of steam, which is the sum of entropies, corre- sponding to the various increments making up the total heat of the steam, depends upon the quality of the steam. For dry saturated steam the total entropy above 32 F. and temperature 7\ is equal to the sum of the entropy of the liquid and the entropy of evaporation for dry saturated steam. This may be written 0sat. = #1 + — (l46) J- 1 = log e -^ + -^ (147) i J- 1 Similarly, for wet steam whose quality is x, the total entropy is 0wet = 01 + -=- (l48) J- 1 , 7\ xLi J- i 1 For superheated steam whose final temperature is T sup . and the temperature corresponding to saturation is 7\, the total entropy is, by equation (144), *_-* + £ +■/•*■*£* • ■ ( I49 ) 1 1 «^r sa t. J- = loge ^ + -£ + C p \0ge -^ ' (i 50) 1 2 J- I JL sat. Values of these entropies will be found in steam tables. Referring to Fig. 25, the line Tic represents the increase of entropy due to the latent heat added during the steaming process. If this steaming process had stopped at some point such that the steam was wet, having a quality x, this condition of the steam could be denoted by the point s, where This relation is obvious, for a distance along Tic represents the entropy of steam, which is proportional to the latent heat added, which in turn is proportional to the amount of dry steam THE MOLLIER CHART 99 rrt formed from one pound of water. In like manner, — ^— is the T 2 d quality of steam at the point m that has been formed along T 2 d at the temperature T 2 . It is thus apparent that any point on a T-cj> diagram will give full information in regard to the steam. The proportional dis- tances on a line drawn through the given point between the water and the dry steam lines and parallel to the X-axis give the quality of the steam as shown above. The ordinate of the point gives the temperature and corresponding pressure, while its position relative to other lines, such as constant volume and constant total heat lines which can be drawn on the same dia- gram, will give further important data. The Mollier Chart. While the temperature-entropy diagram is extremely useful in analyzing various heat processes, its use. in representing the various conditions of steam is not so conven- ient as that of the Mollier chart. This chart is illustrated in Plate 1 of the Appendix. The coordinates consist of the total heat of the steam above 32 F. and entropy. The saturation curve marks the boundary between the superheated and satu- rated regions. In the wet region lines of constant volume are drawn and in the superheated regions the lines of equal super- heats appear. In both the superheated and saturated regions, lines of constant pressure are drawn and the absolute pressures of the various curves are labeled. By means of the Mollier chart (Appendix) the curve for adiabatic expansion can be very readily drawn on a pressure- volume diagram when the initial quality of steam at cut-off is known. Assume that one pound of wet steam at a pressure of 150 pounds per square inch absolute and quality 0.965 dry is admitted to the engine cylinder per stroke, and that there is previously in the clearance space 0.2 cubic foot of steam (see Fig. 26), at exactly the same condition. The volume of a pound of dry saturated steam at this initial pressure of 1 50 pounds is, from the steam-tables, 3.012 cubic feet. At 0.965 quality it will be 1 (0.965 X 3.012) = 2.905 cubic feet. On the IOO ENTROPY scale of abscissas this amount added to the 0.20 cubic foot in the clearance gives 3.105 cubic feet, the volume to be plotted at cut-off. Other points in the adiabatic expansion curve can be readily plotted after determining the quality by the method given on page no. ^7 Clearance Steam Admission t Cut-off 0.20 3.15 Volume of Steam in Cylinder (Cu. ft.) Fig. 26. — Illustrative Indicator Diagram of Engine using Steam with Expansion. Temperature-entropy Diagram for the Steam Power Plant. Fig. 27 illustrates the heat process going on when feed water is received in the boilers of a power plant at ioo° F., is heated and converted into steam at a temperature of 400 F., and then loses heat in doing work. When the feed water first enters the boiler its temperature must be raised from ioo° to 400 F. before any " steaming" begins. The heat added to the liquid is the area MNCD. This area represents the difference between the heats of the liquid (374 — 68) or about 306 B.t.u. The horizontal or entropy scale shows that the difference in entropy between water at ioo° and 400 F. is about 0.436.* The curve NC is constructed by plotting from the steam tables the values of the entropy of the liquid for a number of different temperatures between ioo° and 400 F. If water at 400 F. is converted into steam at that temperature, * As actually determined from Marks and Davis' Steam Tables (pages 9 and 15), the difference in entropy is 0.5663 — 0.1295 or 0.4368. Practically it is im- possible to construct the scales in the figure very accurately. TEMPERATURE-ENTROPY DIAGRAM IOI the curve representing the change is necessarily a constant tem- perature line and therefore a horizontal, CE. Provided the evaporation has been complete, the heat added in the " steaming " process is the latent heat or the heat of evaporation of steam (L) at 400 F., which is approximately 827 B.t.u. 400 • •5100 § 32! u 1 C3 -460 M Supei heated Steam 0.130 .566 1.528 Entropy —

diagram, an adiabatic (isentropic) line is represented by a line parallel to the T-axis, i.e., by a line of constant entropy. If steam is initially wet and is expanded adia- batically, it becomes wetter as a rule.* In general, in any expansion, in order to keep steam at the same relative dryness as it was initially, while it is doing work, some heat must be supplied. If the expansion is adiabatic so that no heat is taken in, a part of the steam will be condensed and will form very small particles of water suspended in the steam, or it will be condensed as a sort of dew upon the surface of the enclosing vessel. The relation between pressure and temperature as indicated by the steam-tables continues throughout an expansion, pro- vided the steam is initially dry and saturated or wet. * When the percentage of water in steam is very great and the steam is ex- panded adiabatically there is a tendency for the steam to become drier. This is very evident from an inspection of diagrams like Fig. 25. HO EXPANSION AND COMPRESSION OF VAPORS Adiabatic Curve for Steam. Whether steam is initially dry and saturated or wet, the adiabatic curve may be represented by the formula: PV n = constant. The value of the index n depends on the initial dryness of the steam. Zeuner has deter- mined the following relation: n = 1.035 + — (i55) 10 Solving this when x = unity (dry and saturated steam) the value of n is 1.135, and when x is 0.75, n has the value 1.11.* While the work during an adiabatic expansion may be cal- culated from the value of n as determined from Zeuner's relation (equation 155), the following method is more commonly used. Since by definition the heat added or abstracted during an adiabatic process is zero, the heat equation becomes, Q = I 2 -h + W = 0, or W = h - 1 2 (156) The work done by an adiabatic process can then be determined by the difference between the internal energies at the beginning and end of the process. In order to calculate the internal energies the qualities must be known and these may be found from the entropies. Quality of Steam During Adiabatic Expansion. Since in an adiabatic expansion no heat transfer takes place, the entropy remains constant, and, therefore, on a T- diagram, this condition is represented by a straight vertical line as cgf (Fig. 25) or smk. Thus for wet steam: cf> = 6 + x-, (157) where x = the quality or dryness fraction of the steam, = * Rankine gave the value of n = V, which obviously from the results given is much too low if the steam is at all near the dry and saturated condition. His value would be about right for the condition when x = 0.75. In an actual steam engine, the expansion of steam has, however, never a close approximation to the adiabatic condition, because there is always some heat being transferred to and from the steam and the metal of the cylinder and piston. QUALITY OF STEAM DURING ADIABATIC EXPANSION III the total entropy of saturated steam, and = the entropy of the water. Since in adiabatic expansion the entropy remains constant, the following equation can be written 0i = 02 (total entropies) or Bi + xM = e 2 + xM- (i 5 8) il 1 2 Knowing the initial conditions of steam, the quality of the steam at any time during adiabatic expansion can be readily determined* Thus, suppose the initial pressure of dry satu- rated steam to be 100 pounds per square inch absolute, and the final pressure after adiabatic expansion 1 7 pounds per square inch. From the steam tables we find that the total entropy 0i, for dry steam at 100 pounds pressure, is 1.6020; that is 0i = 1.6020. The entropies at 17 pounds pressure are also obtained from the tables, 1.6020 = 0.3229 -f- # 2 14215, whence #2 = 0.899. For a rapid and convenient means of checking the above result, the " Total Heat-entropy " diagram in the Appendix can be used. From the intersection of the 100-pound pressure line and that of unit quality (" saturation line") is dropped a vertical line (line of constant entropy = 1.602) to the 17-pound pressure line. This latter intersection is found to He on the 0.90 quality line. Example. One pound of steam having a quality of 0.95 at a pressure of 100 pounds per square inch absolute expands adia- batically to 15 pounds per square inch absolute. 1. What is the quality at the final condition? The total entropy at the initial condition equals + x- = 0.4743 + 0.95 x 1. 1277 = 1.5456. 112 EXPANSION AND COMPRESSION OF VAPORS The total entropy at the end of the expansion equals + x - = 0.3133 + 1.4416 x. Since entropy is constant in adiabatic expansion 0.3133 + 1.4416 s = i.545 6 > from which the final condition is: x = 0.854. 2. How much work is done during the expansion? Since there is no heat added the work done equals the loss in internal energy. The internal energy at the end of the expansion equals h + X2P2 = 181. o + 0.854 X 896.8 = 946.9 B.t.u. The internal energy at the initial condition equals h + Xipi = 298.3 + 0.95 X 806.6 = 1064.6 B.t.u. The work equals 1064.6 — 946.9 = 1 1 7.7 B.t.u. or 91,576 foot-pounds. Poly tropic Expansion {n — 1). Example. One pound of steam has a pressure of 100 pounds per square inch absolute and a quality of 0.95. It expands along an n = 1 curve to 20 pounds per square inch absolute. What is the quality at the end of the expansion? Solution. The volume of the steam at the initial condition is X X F S at. x X F S at. = 0.95 X 4.429 = 4.207 cubic feet. Obviously, PxV? = P 2 V 2 n and since n — 1, 100 X 4.207 = 20 X V2, V 2 = 21.035 cubic feet. The volume of dry saturated steam at the end of the expan- sion or at 20 pounds per square inch is 20.08. Therefore the steam is superheated at end of expansion. How is this known? GRAPHICAL DETERMINATION OF QUALITY OF STEAM 113 Graphical Determination of Quality of Steam by Throttling Calorimeter and Total Heat-entropy Diagram. It will be re- membered that the throttling calorimeter (pages 77 to 81) de- pends for its action upon the fact that the total heat of steam which expands without doing work remains the same, the heat in excess of that required to keep the steam dry and saturated going to superheat the steam. Suppose that steam enters the calorim- d.50 1.60 1.70 1.80 Entropy Fig. 28. — Mollier Diagram for Determining Quality of Steam. eter at a pressure of 150 pounds per square inch absolute, and is throttled down to 1 7 pounds per square inch, the actual tempera- ture being 24o ? F. Since the saturation temperature for steam at 17 pounds pressure is 219.4, the steam in the calorimeter is superheated 240 — 219.4 or 20.6 degrees. In order to find the quality of the live steam refer to the " Mollier Diagram " (Appen- dix or Fig. 28) and find the intersection of the 20.6 degrees super- heat line with the 1 7-pound pressure line. From this point follow 114 EXPANSION AND COMPRESSION OF VAPORS a horizontal line (line of constant total heat) to the left until it intersects the 150-pound pressure line. This point of intersec- tion is found to lie on the 0.96 quality line. Formula 117 (page 80) gives the following result in close agreement with the diagram: _ 1153.1 + 047 (240 ~ 2194) - 330.2 Xl ~ 863.2 = 0.965. PROBLEMS 1. Dry saturated steam at 100 lbs. per sq. in. absolute pressure contained in a closed tank is cooled until its pressure drops to 15 lbs. per sq. in. abso- lute. What is the final quality and the heat removed from each pound of steam? 2. One pound of steam at 15 lbs. per sq. in. absolute has a volume of 1 2.36 cu. ft. It is heated under constant volume until the pressure becomes 50 lbs. per sq. in. absolute, (a) What is the quality before and after the heating? (b) How much heat was supplied? 3. A closed tank containing dry and saturated steam at 15 lbs. per sq. in. absolute pressure is submerged in a body of water at a temperature of 59 F. What will be the ultimate pressure and quality of steam within the tank? 4. Prove that for a constant pressure expansion the heat supplied equals the difference between the total heats of the vapor at the beginning and at the end of the expansion. 5. One pound of steam at 100 lbs. per sq. in. absolute pressure and 50 per cent dry expands at constant pressure. What work is done and what heat is required to double the volume? "What is the temperature at the beginning and at the end of the expansion? 6. One pound of steam at a pressure of 100 lbs. per sq. in. absolute and 50 per cent dry is expanded isothermally until it is dry and saturated. Find the heat supplied and the work done. 7. One pound of steam at a pressure of 150 lbs. per sq. in. absolute has a quality of 0.90. What work is done and what heat is required to double its volume at constant pressure? 8. If steam at 200 lbs. per sq. in. absolute, 95 per cent dry, is caused to expand adiabatically to 228 F., what are the properties of this steam at the lower point? (That is, final total entropy, entropy of evaporation, quality and volume.) 9. What will be the final total heat of dry saturated steam that is ex- panded adiabatically from 150. lbs. per sq. in. absolute down to 10 lbs. per sq. in. absolute? PROBLEMS 115 10. Steam having a quality of 0.20 dry is compressed along an adiabatic curve from a pressure of 20 lbs. per sq. in. absolute to a pressure correspond- ing to a temperature of 293 F. What is the final quality? 11. Determine the final quality of the steam and find the quantity of work performed by 2 lbs. of steam in expanding adiabatically from 250 lbs. per sq. in. absolute pressure to 100 lbs. per sq. in. absolute, the steam being initially dry and saturated. 12. One pound of steam at 150 lbs. per sq. in. absolute, and 200 F. superheat, expands adiabatically. What is the pressure when the steam becomes dry and saturated? What is the work done during the expan- sion? 13. One pound of dry and saturated steam at 15 lbs per. sq. in. absolute pressure is compressed adiabatically to 100 lbs. per sq. in. absolute pressure. What is the quality at the end of the compression and the negative work done? 14. One pound of steam at 100 lbs. per sq. in. absolute pressure has a quality of 0.80. It expands along an n = 1 curve to a pressure of 15 lbs. per sq. in. absolute, (a) What is the volume at the beginning and at the end of the expansion, (b) the quality at the end of the expansion, (c) the work done during the expansion, (d) the heat supplied to produce the expan- sion? 15. One pound of steam at 150 lbs. per sq. in. absolute expands along an n = 1 curve to 15 lbs. per sq. in. absolute. The quality of the steam at 15 pounds is to be dry and saturated, (a) What must be the quality at the initial conditions? (b) What work will be done by the expansion? (c) What heat must be supplied? 16. Steam at a pressure of 100 lbs. per sq. in. absolute having a quality of 0.50 expands adiabatically to 15 lbs. per sq. in. absolute. What is the quality at the end of the expansion? 17. One pound of steam at a pressure of 100 lbs. per sq. in. absolute has a volume of 4 cu. ft. and expands adiabatically to 15 lbs. per sq. in. absolute. (a) What is the quality at the initial and final conditions? (b) What is the work done during the expansion? 18. One pound of steam having a pressure of 125 lbs. per sq. in abso- lute and volume of 4.17 cu. ft. expands adiabatically to 25 lbs. per sq. in. absolute. (a) What is the quality at the initial and final conditions? (b) What is the work of expansion? 19. Given the steam as stated in problem 18 but with expansion complete at 100 lbs. per sq. in. absolute. What is the quality at this pressure? 20. What would be the pressure if the steam in problem 18 were expanded adiabatically until it became dry and saturated? n6 EXPANSION AND COMPRESSION OF VAPORS 21. One pound of steam at a temperature of 360 F. has a quality of 0.50, and expands under constant pressure to a volume of 3.4 cu. ft. (a) What is the quality at the final condition? (b) What is the work of the expansion? (c) What heat is required? 22. Two pounds of steam at a pressure of 100 lbs. per sq. in. absolute have a volume of 4 cu. ft., and expand under constant temperature to a volume of 8 cu. ft. (a) What is the quality at the initial and final conditions? (b) What is the work of the expansion? (c) How much heat is required? CHAPTER VIII CYCLES OF HEAT ENGINES USING VAPORS Carnot Cycle. The Carnot cycle using a vapor employs the same apparatus as was explained on page 40. The cycle is made up of two isothermals and two adiabatics, but differs from the cycle using gas as the working medium in that the isothermal curves are lines of constant pressure. Volume Fig. 29. — Camot Cycle using Vapors. As an illustration, assume that the vapor in the cylinder is in the liquid state and at a temperature T\ when the heat is applied. The heating process continues until the vapor becomes dry and saturated. In order to maintain the temperature constant the heat must be supplied at such a rate as to maintain the pressure constant. The volume increases during this change from that of the specific volume of the liquid to the specific volume of the dry saturated vapor at the temperature TV This change is represented by the lines ah on the PV and temperature-entropy diagrams, Figs. 29 and 30. 117 n8 CYCLES OF HEAT ENGINES USING VAPORS The cylinder is then removed from the source of heat and the adiabatic expansion is produced. This is represented in Figs. 29 and 30 by the curves be. The isothermal compression curve cd is produced when the cylinder is placed in communi- cation with the refrigerator or condenser and heat is absorbed from the vapor. Since the cyl- inder contains a saturated va- por, the process results in a constant pressure curve at tem- perature, r 2 . The adiabatic compression curve da follows when the cyl- inder is removed from the re- frigerator. The vapor in its final condition is reduced to a liquid at the temperature 7\. The heat added to the cycle is that required to produce the line ab, Figs. 29 and 30. For the assumed case this is: <2i = H b - h a = L h (159) where H b = total heat of dry saturated steam at the pressure P b , h a = heat of liquid above 32 F. for condition at a. The heat rejected from the cycle is that absorbed by the refrigerator and for each pound of vapor it is equal to Q2 = (h c + XcL c ) — {h d + XdLa). (160) From the temperature-entropy diagram, Fig. 30, the heat added and heat rejected are Qi = T x (fa - <£«), (161) ft = T 2 (fa - 0d). (162) Since ( c — <*) = (<£& — a), Q 2 = T 2 (» - 4> a ). (163) Entropy-^ Fig. 30. — Temperature-entropy Diagram of Carnot Cycle using Vapors. THE RANKINE CYCLE 119 The work of the cycle may be determined from the algebraic sums of the work under the individual curves, but can be more simply calculated from the temperature-entropy diagram, Fig. 30. The area abed is proportional to the work and since it is a rectangle, work of cycle = (T 2 — 7\) ( — <£ a ). From equations (161) and (163), the efficiency of the cycle is 77 _ (T2 — Ti) ((f> b — a ) T\ (& — a) T 2 -T x (164) Equation (164) shows that the efficiency of Carnot's cycle is not affected by the character of the working substance and is dependent only upon its initial and final temperatures. The Rankine Cycle.* The Carnot cycle gives the maximum efficiency obtainable for a heat engine operating between given limits of temperature. In order that a steam engine may work on a Carnot cycle, the steam must be evaporated in the cylinder instead of in a separate boiler, and condensed in the cylinder instead of being rejected to the air or to a separate condenser. Such conditions are obviously impracticable, and it has, therefore, been found necessary to adopt some other cycle which conforms more with practical conditions. The most efficient practical steam cycle, and the one which has been adopted as the standard with which the efficiency of all steam engines may be compared is the Rankine Cycle. The pressure- volume diagram of this cycle is shown in Fig. 31. Steam is admitted at constant pressure and temperature along ab to a cylinder without clearance. At b cut- off occurs, and the steam expands adiabatically from b to c, some of i condensing during the process. The steam is then dis- charged at constant pressure and temperature along the back pressure line cd. Line da represents the rise in temperature and * Also known as the Clausius Cycle, having been published simultaneously and independently by Clausius. 120 CYCLES OF HEAT ENGINES USING VAPORS pressure at constant volume when the condensed steam is con- verted into a vapor. The four stages of the Rankine cycle may be stated as follows: (i) Feed water raised from temperature of exhaust to tem- perature of admission steam. (Line da.) (2) Evaporation at constant admission temperature. (Line ab.) (3) Adiabatic expansion down to back pressure. (Line be.) (4) Rejection of steam at the constant temperature corre- sponding to the back pressure. (Line cd.) Volume Fig. 31. — Indicator Diagram of Ideal Rankine Cycle. The net work done in the cycle, assuming one pound of wet steam, is calculated as follows: 1. External work of evaporation (in B.t.u.), (W») = tIs (PiFi*i). (165) 2. Loss in internal energy, (W bc ) = fa + Km — (fa + X2P2) B.t.u. (166) 3. External work of evaporation at temperature of exhaust (B.t.u.), W dc = - Thf (PcVc) = - T^8 (P2V 2 X 2 ). (167) 4. W da - O. (168) THE RANKINE CYCLE 121 Adding, Net work of cycle, W = -ffaPiViXi + hi + xipi - h- x 2 p 2 — TT 8" -P2 V 2 X 2 , but •yyg P^V\ + pi — -£1. Therefore, Tf = h + X1Z1 - (fe + x 2 L 2 ) (B.t.u.). (169) Thus the net work of the Rankine cycle is equal to the dif- ference between the total heat of the steam admitted and the total heat of the steam exhausted. This statement applies whether the steam is initially wet, dry or superheated. The heat added during the cycle is Qi = h a + -XbLj, — h d . (170) The heat rejected during the cycle is Q 2 = XcLc. (171) The efficiency of the Rankine cycle is E __ Qi— Q2 = h a + x b L b — ha — XcLc t Qi h a + x^ — h d Since h a = h b and h c = h d , 77 f^b ~~ X^L,^ He XcL/c / \ rt b -j- XfrL b lie Fig. 32 is the T- diagram for a Rankine cycle using dry saturated steam. The letters abed refer to the corresponding points in the pressure- volume diagram Fig. 31. The net work of the cycle is the area B + C, which is the difference between the total heats at admission and exhaust. The heat added per cycle is represented by the areas A + B + C + D and the B + C Thermal efficiency = A + B + Q + D (173) hi + X\Li — h 2 — x 2 L 2 ( \ = j — ; j 7 ^74; hi + X1L1 — rh * The final quality can be determined by equation (158). 122 CYCLES OF HEAT ENGINES USING VAPORS fe in the denominator must always be subtracted from hi + X\L\ (the total heat above 3 2° F.), in order to give the total heat above the temperature of feed water, which in engine tests is always assumed for the purpose of comparison to be the same as the exhaust temperature. Entropy— Fig. 32. — Temperature-entropy Diagram of Rankine Cycle. Example. One pound of steam at a pressure of 160 pounds per square inch absolute and quality of 0.95 performs a Rankine cycle exhausting at 5 pounds per square inch absolute. 1. What is the quality of the exhaust? The total entropy at the initial condition = 0.5208 + 0.95 X 1.0431. The total entropy at the exhaust = 0.2348 + 1.608 x. Then 0.5208 + 0.95 X 1.0431 = 0.2348 + 1.6084 #. From which x = 0.794. 2. What is the net work of the cycle? Work = Hi - H 2 = 335.6 + 0.95 X 858.8 - 130.1 - 0.794 x 1000.3 = 227.2 B.t.u. 3. What is the efficiency of the cycle? THE RANKINE CYCLE 123 Efficiency = 227.2 335.6 + 0.95x858.8-130.1 = 0.222 or 22.2 per cent. In the actual steam engine cycle it is impractical to expand the steam down to the back-pressure line. The Rankine cycle for the actual steam engine is similar to that described, except that the adiabatic expansion terminates at a pressure higher than that of the back-pressure, that is, the expansion is incomplete. The pressure-volume and T-4> diagrams of this modified Rankine cycle using dry saturated steam are shown in Figs. 33 and 34. The cylinder is without clearance. Steam is admitted Volume Fig. 33. — Rankine Cycle, Incomplete Expansion. at constant pressure and temperature along ab. Cut-off occurs at point b and the steam expands adiabatically to the terminal pressure c. Part of the steam is discharged at constant volume cd. The remainder is exhausted during the back-pressure stroke de. Line ea represents the rise in temperature of the feed water from T 2 to 2\. The net work of the cycle can best be calculated by dividing Fig* 33 into the two areas abed and e'ede. The area abed is that of the theoretical or ideal Rankine cycle, while dede is that of the rectangle. The net work of the cycle is equal to the sum of these two areas. 124 CYCLES OF HEAT ENGINES USING VAPORS The heat equivalent of the area abed is hb + XbLb — h c — XcL c . The area e'ede is Tb (Pc - Pa) (Va - o). The total heat equivalent of the work of the cycle is (Pc - Pa) Va h + XbLb — h c — XcLc + The heat added to the cycle is hb + XbLb — ha. The efficiency of the cycle is 778 hbXbLb — h c —XcLc + E = {Pc - Pa) Va 778 * hb + XbLb — ha (i75) (176) (i77) (178) (i79) In the T- diagram, Fig. 34, the letters abede refer to corresponding points in the pressure-volume diagram (Fig. 33). The net work of the cycle is represented by the area B + C. The heat added to the cycle is represented by the area A + B + C + D. The incomplete Rankine cy- cle (Figs. 33 and 34) is less efficient than the ideal cycle (Figs. 31 and 32), because of failure to expand the steam completely. This loss is repre- sented in Figs. 33 and 34 graphi- cally by the area cdf. This cycle is sometimes used as a standard in preference to the ideal Rankine cycle when the efficiencies of engines are com- pared. Example. One pound of steam at a pressure of 160 pounds per square inch absolute and quality of 0.95 goes through a Entr.opy-0 Fig. 34. — Rankine Cycle, Incomplete Expansion. THE PRACTICAL OR ACTUAL STEAM ENGINE CYCLE 125 Rankine cycle. The terminal pressure is 15 pounds per square inch absolute and the exhaust pressure 5 pounds per square inch absolute. What is (a) the work of the cycle, (b) the heat added to the cycle, and (c) the efficiency of the cycle? Solution. The total entropy of the steam at the initial con- dition is 0.5208 + 0.95 X 1.0431. The total entropy of the steam at the terminal pressure is 0.3133 + x (1.4416). Then 0.5208 + 0.95 X 1.0431 = 0.3133 + x (1.4416) from which the quality at the terminal pressure is x = 0.831. The volume of the steam at the terminal pressure is 0.831 X 26.27 = 21.83. The total heat of the steam at the initial condition is 335.6 + 0.95 X 858.8 = 1151.5. The total heat of the steam at the terminal pressure is 181.0 + 0.831 X 969.7 = 986.8. The work of the cycle is then (in terms of heat units), Trr on o . ( T 5 ~ 5) X X 44 X 21.83 w = 1151.5 - 986.8 + ^-2 — D/ r* * = 205.1. 778 The heat added to the cycle is 335.6 + 0.95 x 858.8 — 130.1 = 1021.4 B.t.u. The efficiency of the cycle is = 20.08 per cent. 1 02 1. 4 The Practical or Actual Steam Engine Cycle. In the steam engine designed for practical operation it is impossible to expand the steam down to the back-pressure line; and, furthermore, it 126 CYCLES OF HEAT ENGINES USING VAPORS is evident that some mechanical clearance must be provided. The result is that in the indicator diagram from the actual steam engine, we have to deal with a clearance volume, and both incom- plete expansion and incomplete compression as shown in Fig. 35. In order to calculate the theoretical efficiency of this prac- 9 b c\ h a % [ 83 \ - Volume Fig. 36. — Indicator Diagram of an Engine using Steam without Expansion. 128 CYCLES OF HEAT ENGINES USING VAPORS E = work done = (P x - P 4 ) (F 2 - V x ) ^ . g , heat taken in 778 (x^Li + h — fe) ? where the denominator represents the amount of heat taken in, with the feedwater at temperature of exhaust, t 2 . In actual practice the efficiency of engines using steam without expansion is about 0.06 to 0.07, when the temperature of condensation is about ioo° F. When steam is used in an engine without ex- pansion and also without the use of a condenser the value of this efficiency is still lower. It will be observed that under the most favorable conditions obtainable the efficiency of an engine without expansion cannot be made under normal conditions to exceed about 7 per cent. In the actual Newcomen steam engines the efficiency was very much lower than any of the values given because at every stroke of the piston a very much larger amount of steam had to be taken in than that corresponding to the volume swept through by the piston on account of a considerable quantity of steam condensing on the walls of the cylinder. Adiabatic Expansion and Available Energy. A practical ex- ample as to how the temperature-entropy diagram can be used to show how much work can be obtained by a theoretically per- fect engine from the adiabatic expansion of a pound of steam will now be given. When steam expands adiabatically — with- out a gain or loss of heat by conduction — its temperature falls. Remembering that areas in the temperature-entropy diagram represent quantities of heat and that in this expansion there is no exchange of heat, it is obvious that the area under a curve of adiabatic expansion must be zero ; this condition can be satisfied only by a vertical line which is a line of constant entropy. The work done during an adiabatic process, while it cannot be obtained from a "heat diagram," can very readily be determined from the area under the adiabatic curve of a pressure-volume diagram, or better still by the use of steam- tables as follows: In an adiabatic expansion the amount of work done is the mechani- cal equivalent of the loss in internal energy as explained in Chap- ter III. Therefore, it is only necessary to determine the internal ADIABATIC EXPANSION AND AVAILABLE ENERGY 129 energy of the steam at the beginning and end of the adiabatic expansion. h = h x + Xipi, (182) I 2 = h 2 + x 2 p 2 . (183) Work during adiabatic expansion = loss in internal energy W = (hi + Xipi — Jh — X2P2) 778 (foot-pounds). (184) Fig- 37 is a temperature-entropy diagram representing dry saturated steam which is expanded adiabatically from an ini- tial temperature Z\ (corresponding to a pressure Pi) to a lower final temperature T 2 (corresponding to a pressure P 2 ), The C / T, P, \ E JlBB "J ^^^^^^^^^ G \ g 1 F F' & Entropy a -r 2 Fig. 37. — Temperature-entropy Diagram for Dry Saturated Steam Expanded Adiabatically. initial and final conditions of total heat (H) and entropy (i) 2V* (185) * It should be observed that this form is for the case where the steam is initially dry and saturated. For the case of superheated steam a slightly differ- ent form is required. 130 CYCLES OF HEAT ENGINES USING VAPORS An application of this equation will be made to determine the heat energy available from the adiabatic expansion of a pound of dry saturated steam from an initial pressure of 165 pounds per square inch absolute to a final pressure of 15 pounds per square inch absolute. Example. Pi = 165 7\ = 826 degrees, from steam tables. P 2 = IS T 2 = 673.0 #1 = 1195.0B.tu. " #2 = 1150.7 B.t.u. " 01 = I-56I5 X = Xi 7jT + 01, 01 — #6 = -J (i — #l). 1 1 ll 132 CYCLES OF HEAT ENGINES USING VAPORS Example. Calculations for the velocity resulting from adia- batic expansion for the same conditions given in the preceding example, except that the steam is initially 5 per cent wet, are given below. Pi = 165 lbs. absolute. Ti = 826 degrees from tables P 2 = 15 lbs. absolute. T 2 = 673.0 degrees Hi = 1195.0 B.t.u. H 2 = 1150.7 " 0i = 1.5615 02 = 1-7549 Li = 856.8 B.t.u. Xi = 1. 00 — 0.05 = 0.95 E c (1195.0 - 1150.7) + (i.7549 - 1-5615) 673 - 856.8 826 X (i - 0.95) (826 - 673) = 44.3 + 130.2 - 7.93 Eaw = 166.5 B.t.u. per pound of wet steam V = 223.8 VeZ = 223.8 x V166.5 = 223.8 X 12.9 = 2886 feet per second. This result can be checked very quickly by the "total heat- entropy" or "Mollier" diagram (Appendix). The intersection of the 0.95 quality line and 165 pounds pressure line is found to lie on the n 52 B.t.u. total heat line. Since the expansion is adiabatic, the entropy remains constant. Therefore, following the vertical or constant entropy line (entropy = about 1.507) down to its intersection with the 1 5 pounds pressure line, we find that the total heat at the end of adiabatic expansion is 985 B.t.u and 1 152 — 985 = 167 B.t.u. available energy, as above. If the steam were initially superheated, the available energy during adiabatic expansion could be obtained in the same way by means of the diagram. Available Energy of Superheated Steam. The amount of energy that becomes available in the adiabatic expansion of superheated steam is very easily expressed with the help of Fig. 39. Two conditions after expansion must be considered: AVAILABLE ENERGY OF SUPERHEATED STEAM 1 S3 (i) When the steam in the final condition is superheated, (2) When the steam in the final condition is wet (or dry saturated). Using Fig. 39 with the notation as before except E as is the avail- able energy from the adiabatic expansion of steam initially super- heated in B.t.u. per pound, S and H s are respectively the total entropy and the total heat of the superheated steam at the T 3 H3 l* Ti Entropy — Fig. 39. — Temperature-entropy Diagram for Superheated Sxeam. initial condition, then from the diagram, when the steam is wet at the final condition, • E fls = H S -H 2 + (0 2 - s ) T 2 . (189) When the steam is superheated at the final condition, E as = H s - H 2 ; - (0, - 2 O TV. (190) It will be observed that these equations (189) and (190) are the same in form as (184), and that equation (190) differs only in hav- 134 CYCLES OF HEAT ENGINES USING VAPORS ing the terms H s and fa in the place of Hi and fa. In other words equation (184) can be used for superheated steam if the total heat and entropy are read from the steam tables for the required degrees of initial superheat. The following examples illustrate the simplicity of calcula- tions with these equations: Example 1. Steam at 150 pounds per square inch absolute pressure and 300 F. superheat is expanded adiabatically to 1 pound per square inch absolute pressure. How much energy in B.t.u. per pound is made available for doing work? Solution. H s = 1348.8 B.t.u. per pound, H 2 = 1 103.6 " fa = 1.980, 4>> = i-73 2 > . T 2 = 559-6° F, Eas = I348.8 - IIO3.6 + (1.980 - I.732) 559.6 = 383.9 B.t.u. per pound. The result above may be checked with the total heat-entropy chart (Appendix) and obtain thus (1349 — 967) or 382 B.t.u. per pound. Example 2. Data the same as in preceding example except that the final pressure is now 35 pounds per square inch absolute. (Final condition of steam is superheated.) Calculate Eas. Solution. H s = 1348.8 B.t.u. per pound, HJ = 1 166.8 " " " fa = 1.732, fa' = 1.6868, TV = 718.9° F., Eas = 1348.8 - 1166.8 - (1.7320 - 1.6868) 718.9 = 149.5 B.t.u. per pound. Application of Temperature-entropy Diagram to Analysis of Steam Engine. The working conditions of a steam engine, as stated before, can be shown not only by the indicator card, but also by the employment of what is known as a "temperature- APPLICATION OF TEMPERATURE-ENTROPY DIAGRAM 135 entropy" diagram. This diagram represents graphically the amount of heat actually transformed into work, and in addition the distribution of losses, in the steam engine. For illustration, a card was taken from a Corliss steam engine having a cylinder volume of 1.325 cubic feet, with a clearance volume of 7.74 per cent, or 0.103 cubic feet; the weight of steam in pounds per stroke (cylinder feed plus clearance) was 0.14664 pounds. Barometer registered atmospheric condition as 14.5 pounds per square inch. The scale of the indicator spring used in getting the card was 80 pounds to the inch. Steam chest pressure was taken as 153 pounds per square inch (absolute), and a calorimeter determination showed the steam to be dry and saturated. The preliminary work in transferring the indicator card to a T- diagram, consists first in preparing the indicator card as follows: It was divided into horizontal strips at pressure intervals of 10 pounds with the absolute zero line taken as a reference; this line was laid off 14.5 pounds below atmospheric conditions. (See Fig. 40.) For reference, the saturation curve was drawn. Knowing the weight of steam consumed per stroke and the specific volume of the steam (from the Steam Tables), for various pressures taken from the card, the corresponding actual volumes could be obtained; this operation is, merely, weight of steam per stroke multiplied by specific volume for some pressure (0.14664 X column 5 in the table below), the resulting value be- ing the volume in cubic feet for that condition. These pressures and volumes were plotted on the card and the points joined, re- sulting in the saturation curve, 2 // -6"-8 // -o/ / . The next step consisted in constructing the " transformation table " with the columns headed as shown. All the condensing and evaporation processes are assumed to take place in the cylin- der and the T-cf> diagram is then worked up for a total weight of one pound of steam as is customary. Column 1 shows the re- spective point numbers that were noted on the card; column 2, the absolute pressures for such points; column 3, the corre- sponding temperatures for such pressures; column 4, the vol- 136 CYCLES OF HEAT ENGINES USING VAPORS ENTROPY DIAGRAM 1.0 Entropy Fig. 40. — Temperature-entropy Diagram of Actual Steam Engine Indicator Diagram. APPLICATION OF TEMPERATURE-ENTROPY DIAGRAM 137 ume in cubic feet up to the particular point measured from the reference line of volumes; column 5, the specific volume of a pound of dry and saturated steam at the particular pressure (Steam Tables); column 6, the volume of actual steam per pound, obtained by dividing the volumes in column 4 by 0.14664 pound (total weight of steam in cylinder per stroke) ; column 7, the dryness fraction "x," found by dividing column 6 by column 5 ; column 8 is the entropy of evaporation ( — J f or particular con- ditions (Steam Tables); column 9 is the product of column 7 and column 8; column 10 is the entropy of the liquid at various conditions as found in the Steam Tables; column 11 is the sum of column 9 and column 10, giving the total entropy. TRANSFORMATION TABLE I 2 3 4 5 6 7 8 9 IO 11 u 0> .a 6 a u xn u 1-4 O.S •^ s.s >8 in ."gto "c3 CJ»- ' _ C8 «... O ft** -1 8 6 3 O w > CO C O .2 P. njH O U \ 'B a"— u a a 2 H 1 2 5 9 12 is 18 20 145 140 I20 48 20 8 8 3° 356 353 34i 279 228 183 183 250 0.1050 0.2250 0.4230 0.8500 1 .4225 0.9758 0.3500 0.1825 3 3 3 8 20 47 47 13 11 22 73 84 08 27 27 74 0.716 1-536 2 .89O 5-8io 9.700 6.660 2.390 1.245 0.2302 0.4770 0.7740 0.6580 0.4830 0.1410 . 0506 0.0907 I .0612 I .0675 1-0954 1-2536 1-3965 1-5380 1-5380 I-33H O . 2440 O . 5090 0.8475 O.825O O.674O 0.2l68 O.O778 O . I 208 0.5107 0.5072 0.4919 0.4077 0-3355 0.2673 0.2637 0.3680 0.7547 1 .0162 1-3394 1.2327 1.0095 0.4841 0-345I 0.4888 Above table is employed for transferring the P-V diagram to the T- diagram. After this table was completed, columns 3 and 1 1 were plotted (Fig. 40). Convenient scales were selected, the ordinates as tem- peratures and the abscissas as entropies. The various points, properly designated, were connected as shown on the T- dia- gram, the closed diagram resulting. This area shows the amount of heat actually transformed into work. This diagram is the actual temperature-entropy diagram for the card taken and may 138 CYCLES OF HEAT ENGINES USING VAPORS • be superimposed upon the Rankine cycle diagram in order to determine the amount and distribution of heat losses. The water line, A-A', and the dry steam line, C-C , were drawn directly by the aid of Steam Table data, i.e., the entropy of the liquid and the entropy of the steam taken at various temperatures, and plotted accordingly. Before the figure could be studied to any extent, the theoreti- cal (Rankine) diagram had to be plotted, assuming that the steam reaches cut-off under steam-chest conditions; that it then ex- pands adiabatically down to back pressure and finally exhausts at constant pressure to the end of the stroke without compres- sion. This diagram is marked, A-C-E-H, on the T-4> plane. The steam-chest pressure of 153 pounds per square inch absolute fixes the point, C, when the temperature line cuts the steam line, C-C . The rest of the cycle is self-evident. Referring to the T- diagram, Fig. 40, H-A-C-E is the Ran- kine cycle with no clearance for one pound of working fluid. The amount of heat supplied is shown by the area, Mi-H-A-C-N, and of this quantity, the area M\-H-E-N * would be lost in the exhaust while the remainder, H-A-C-E, would go into work. This is theoretical, but in practice there are losses, and for that reason, the Rankine cycle is used merely for comparison with the actual card as taken from a test. The enclosed irregu- lar area, 1-2-3 • • • 22-2 3> * s the amount of heat going into actual work. By observation, it is evident that a big area re- mains; this must represent losses of some sort or other. That quantity of work represented by the area, i-5-5 / -i / , is lost on account of wire-drawing; the area $'-C-D-F shows a loss due to initial condensation; the loss due to early release is shown by the area F-12-14-F' for the real card, and by D-G-E for the modified Rankine cycle (such a loss, in other words, is due to incomplete expansion); that quantity represented by 22-B-i f -i is lost on account of incomplete compression, and H-A-B-iS is * The areas Mi HACN and Mi HEN should have added to them, the rectangu- lar area between MiN, and the absolute zero line, which is not shown on the diagram (Fig. 40). APPLICATION OF TEMPERATURE-ENTROPY DIAGRAM 139 1.6 2.0 Entropy Fig. 41. — Temperature (absolute) -entropy Diagram of Actual Steam Engine Indicator Diagram. 140 CYCLES OF HEAT ENGINES USING VAPORS the loss due to clearance. The expansion line from 5 on to 9 in- dicates that there is a loss of heat to the cylinder walls, causing a decrease of entropy; from 9 on to 10, re-evaporation is taking place (showing a gain of entropy). All of the heat losses are not necessarily due to the transfer of heat to or from the steam, as there may be some loss of steam due to leakage. In general, however, the T- diagram is satis- factory in showing heat losses. Fig. 41 was constructed for the purpose of showing how the actual thermal efficiency and the theoretical thermal efficiency (based on the Rankine cycle) can be obtained from the T- diagram. The letters in Fig. 40 refer to the same points as in Fig. 41, the only difference between the two diagrams being the addition of the absolute zero temperature line to Fig. 41. Thermal efficiency = Actual thermal efficiency = Work done Heat added Shaded area W M^H-A-C-N'' = —7^ — . (Planimeter) 20.00 sq. in. = 0.096, or 9.6 per cent.* Rankine cycle efficiency (theoretical thermal efficiency) H-A-C-E " Mi'-H-A-C-N'' = ~.* " (by planimeter) 20.00 = 0.203, or 20.3 per cent. Combined Indicator Card of Compound Engine. The method of constructing indicator diagrams to a common scale of vol- * This value may be regarded as the actual thermal efficiency for one stroke. inasmuch as in the succeeding strokes the "cushion" steam will be used over and over again and hence will not constitute a heat loss. The actual thermal efficiency W of a steam engine under running conditions would then be given by , ^rff where 18 BCE is a Rankine cycle with clearance and complete compression. COMBINED INDICATOR CARD OF COMPOUND ENGINE 141 ume and pressure shows where the losses peculiar to a compound steam engine occur, and, to the same scale, the relative work areas. As the first step divide the length of the original indicator dia- grams into any number of equal parts (Fig. 42), erecting per- pendiculars at the points of division. In constructing a combined card, select a scale of absolute pressure for the ordinates and a scale of volumes in cubic feet 145.6* S7.ir Zero Line Fig. 42. — High and Low Pressure Indicator Diagram of Compound Steam Engine. for the abscissas. To the scale adopted draw in the atmos- pheric pressure (" at.") line, see Fig. 43. Lay off the low-pressure clearance volume on the x-axis to the scale selected. In like manner lay off the piston displace- ment of the low-pressure cylinder and divide this length into the same number of equal parts as the original indicator diagrams were divided. From the original low-pressure card (Fig. 42), de- termine the pressures at the points of intersection of the perpen- diculars erected above the line of zero pressure, taking care that the proper indicator-spring scale is used. Lay off these pressures along the ordinates (Fig. 43), connect the points and the result will be the low-pressure diagram transferred to the new volume and pressure scales. 142 CYCLES OF HEAT ENGINES USING VAPORS The high-pressure diagram is transferred to the new volume and pressure scale by exactly the same means as described for the low-pressure diagram. The saturation curve is next drawn. This curve represents the curve of expansion which would be obtained if all the steam in the cylinder was dry and saturated. It is very probable that the saturation curve for each cylinder will not be continuous since the weight of the cushion steam in the low-pressure cylin- der is usually not the same as that in the high-pressure cylinder. The saturation curve would be continuous for the two cards only when the weight of cushion steam in the high-pressure and low- pressure cylinders is the same (assuming no leakage or other losses). On the assumption that the steam caught in the clearance spaces at the beginning of compression is dry and saturated, the weight of the cushion steam can be calculated from the pressure at the beginning or end of compression, the corresponding cylin- der volumes and the specific volumes corresponding to the pres- sure (as obtained from steam- tables). The total weight of steam in the cylinder is the weight of steam taken into the engine per stroke plus the weight of steam caught in the clearance space (cushion steam). The saturation curves may now be drawn by plotting the volumes which the total weight of steam will occupy at different pressures, assuming it to be dry throughout the stroke. The quality curve (Fig. 43) shows the condition of the steam as the expansion goes on. At any given absolute pressure, the volume up to the expansion line shows the volume of the wet vapor, while the volume up to the saturation curve shows the volume that the weight of the wet vapor would have if it were dry. Thus at any given absolute pressure, the ratio of the vol- ume of the wet vapor (as given by the expansion line of the indicator card) to the total volume of the dry vapor (as obtained from the saturation curve) is the measure of the quality of the steam. Showing the quality by the use of the figure, we have Vol. COMBINED INDICATOR CARD OF COMPOUND ENGINE 143 160 155 150 145 140 135 130 125 120 115 110 105 100 ^95 cr <» 90 Ft D f«85 £ § 80 o S 75 70 65 60 55 60 45 40 85 30 25 20 15 10 5 155 61* H. P. Qua lity < "urvk 100 * y \r 175* \ 1 \l45 .6# |'l Q.P. £ atui altioi lCu •ye r a & |c I .1 0.61 # \ \ \ \ \ \ I LP. Cai \ \ i 1 ^ Qi A Jr. mIe =4§.5 .p.\ \ \ \ L. ?.Qi lalit; Cui •ve j 75* \ \ ! E 0* X 1 * ita! 56 * 1 11* — J37. v. 27.96 £ 428. 36# s \ -..f L.P Sati irati on C urve / L •P Cai d ■s ^^^ / A v\JM.E P.= 11.22 l Ltm. Lin" _L 4l2.7< 5* """ *-— ■ — 1 — "da # -■-t* ? -6.76 ,5 1 1.5 2 2.5 3 3.5 4 4.5 Volume- Cu. Ft, Fig. 43. — Combined Indicator Diagrams for Compound Engine. 144 CYCLES OF HEAT ENGINES USING VAPORS ab -v- Vol. ac = quality. By laying off this ratio from a hori- zontal line to any scale desired as shown, the quality curve may be constructed. Hirn's Analysis. In the study of steam-engine performance the action of the steam in and the influence of the walls of the cylinder become a matter of considerable importance. The amount of heat lost, restored and transformed into work as a result of variation in the condition of the steam throughout the engine-cycle can be determined either by means of the entropy- temperature diagram, or by calorimetric method based on Hirn's theory. The calorimetric method, or more popularly called Hirn'r, Analysis, was developed by Professor V. Develshauvers-Devy of Liege. (See Table of the Properties of Steam by V. Devels- hauvers-Devy, Trans. Am. Soc. Mech. Eng., Vol. XI; also Pea- body's Thermodynamics.) In order to apply Hirn's Analysis to engine testing besides the usual readings the following items must be determined : i. Absolute pressures at cut-off, release and compression from indicator cards, 2. Per cent of stroke at cut-off, release and compression from indicator cards, 3. Weight of steam per stroke determined by weighing the condensed steam or boiler feed water and computing the steam used per stroke, 4. Weight of the cooling water and its temperature at inlet and outlet from condenser, 5. Temperature of the condensed steam. Let w = pounds of steam supplied to the cylinder per stroke at pressure p and quality x. Then the amount of heat brought in by the steam into the cylinder per stroke, Q = w (h + xL), (191) where L = heat of vaporization and h = heat of the liquid above the freezing point. HIRN'S ANALYSIS 145 At the end of compression a certain amount of steam is left in the clearance space and this steam mingles with the w pounds of steam at admission. Calling the weight of the steam caught in the clearance space Wi, the total amount of steam at admission is w -f- w\. According to thermodynamic laws the addition of heat to a substance produces in that substance internal and external changes, the internal changes being volume and temperature variations which are called intrinsic energy changes, while the Volume Fig. 44. — The Steam Engine Cycle. external changes are changes in external potential energy or work done. Thus the steam brought into the cylinder per stroke on account of its available heat produces intrinsic energy changes and is capable of doing external work in overcoming resistance. On the other hand the steam W\ caught in the clearance space at compression is able to produce only internal or intrinsic energy changes. The intrinsic energy changes can be calculated knowing the heat equivalent of internal work or internal latent heat (p) and the heat of the liquid Qi) . The external work can be deter- mined from the indicator cards. Referring to Fig. 44 and calling the heat absorbed by the cylinder walls during admission and expansion Q a and Q b ', that restored during exhaust and compression Q c and Q d ] the intrinsic 146 CYCLES OF HEAT ENGINES USING VAPORS energy at the points of admission, cut-off, release, and compres- sion /1, I 2 , Iz, I *', the external work in heat units AW a , AW b , AW C , AWd, during the events of the stroke, where A = t™; also if the temperature of the condensed steam is t s and that of the cooling water U and U at inlet and outlet, the total weight of cooling water used being G, we have the following relations: Qa = Q + h ~ h ~ AWa. (192) Q b = h-h- AW b . (193) Q c = I3 — I4 — wh s — G (h — hi) — AW C . (194) Q d = h-h + AW d . (195) In equations (192), (193), (194), and (195) Q can be determined from Q = w (h + xL). The values of G can be determined by weighing cooling water; h , ht, and h s by taking the temperature t 0i U, and t s by thermometers and finding h , hi, and h s from steam tables. The intrinsic energy at the events of the stroke are calcu- lated by means of the following equations: h = Wi (h + tfipi), (196) h = (wi -J- w) (h 2 + X2P2), (197) h = (wi + w) (h z + ^sPs), (198) 7 4 = Wi (h + ^4p4), (199) in which W\ — weight of steam caught in clearance space. w — weight of steam brought into the cylinder per stroke. hi, 1h, h z , hi = heat of the liquid at events of stroke. Pi, p2, P3, pi = internal latent heats at the events of stroke. %i, x 2 , x 3 , x± = quality of steam at events of stroke. From the above it is evident that Xi, x 2 , x 3 , #4, and w are un- known, these values being determined by the following procedure: The volume of w pounds of steam in cubic feet is V = w (xu + 0). (200) x = quality of steam, u = the increase in volume produced by the vaporization of one pound of water of volume a into dry CLAYTON'S ANALYSIS OF CYLINDER PERFORMANCE 147 steam of volume S, or u = S — a. Calling the volume of the steam caught in the clearance space Vi and that at cut-off, release and compression V 2 , V3, F 4 , Vi = Wi(xiUi + a). (201) Vi + V 2 = (w + Wi) (x 2 u 2 + a). (202) Vi + V 3 = (w + Wi) (X3U3 + a). (203) Vi + Va = W\ (X4U4 + (208) H V 2 g X 778/ / V 2 \ Superheated Vapor, h + \L ) F V 2 g X 778/ +c y (r SUP -r sa t.)- jP(w 7 z;sat) , (209) 778 V 2 where is the kinetic energy in B.t.u. per pound of the 2 g X 778 substance as it passes a section, V = velocity in feet per second and g = 32.2 feet. If Q represents in B.t.u. per pound the heat units added to the substance between the sections A and B (Fig. 45), the energy equation for air and similar gases can be found by equating the total heat energy put in at A plus the energy added between A and B to the energy discharged at B. This general formula reduces to F 2 2 - TV = 2 g [j^ (P 1 v 1 - P 2 v 2 ) + 778 <2~j or = 2 g X 778 [C 9 (Xi - T 2 ) + Q]. (210) * See equation (61). 152 FLOW OF FLUIDS This thermodynamic equation is the usual form for the flow of air or similar gases. The energy equation for superheated steam can be derived by the use of the same general formula stated above, on the assumption that the substance is superheated at A and B. This formula reduces to -= [h + L\ + C p (r si ,p. — Taa,t)i] 2 g X 778 — [h 2 + l 2 + c P (r SUP . — r sa t.) 2 ] + Q, (211) or V 2 2 — V1 2 = 2 g X 778 [Tabular heat content* — Tabu- lar heat content^ + Q], (212) From a thermodynamic standpoint, the relation between the initial and final condition is that of adiabatic expansion when all the heat which disappears as such is used in changing the veloc- ity, provided the nozzle is properly shaped and Q is zero. The diagram in Fig. 46 represents this condition of affairs on a tem- perature-entropy diagram for air and similar substances. The area acdf is C v (T 2 — 492), and the area abef is C p ( Ji — 492). The quantity of heat energy changed into kinetic energy is there- fore the area bcde and is the difference between the internal energy in the substance at the beginning and end of the opera- tion, together with the excess of work done to maintain the pres- sure of P± at A over the pressure of P 2 at B. The line cd would incline to the right if heat were added in the nozzle, since the effect would be to increase the velocity or increase the area cdeb. The line cd would incline to the left from c if heat were lost, since the area cdeb would decrease. In Fig. 47 the diagram represents the conditions for super- heated vapor. The area aa'cdf represents the heat required to raise the substance from a liquid at 32 F. to superheated vapor at the temperature of Tisup. The area ab'bdf is the heat con- tent at b, the final condition. The area a'cbb' represents, there- fore, the heat available for increasing the velocity. The areas * Tabular heat content means the total heat of superheated steam as read from tables of the properties of superheated steam. FLOW THROUGH A NOZZLE OR ORIFICE 153 representing the heat available for increasing the velocity in Fig. 46 and Fig. 47 are shown by the cross-hatched area in Fig. 48 and are really the representation of the work done (theoretically) in an engine giving such an indicator diagram. Evidently the greater the drop in pressure, the greater will be the cross-hatched area in Fig. 48 and the greater will be the velocity, T 2 c n T, g\ V a/ 492 T.- Ent.- Diagram i 1 / la d\\ t^up. OJ Tjsat. a' 1 T 2 sup. / \ 6 T2 sat. / \ r U T.-Ent.-Diagram d Fig. 46. — Temperature- entropy Diagram of Heat Available in Air. Fig. 47. — Temperature-entropy Dia- gram of the Heat Available in Superheated Steam for Increasing Velocity. regardless of the substance. The line ab in Fig. 49 represents p the velocity curve with V as ordinates and -^ as abscissas, but " 1 since with any substance ex- ! i panding the weight of a cubic foot decreases as the pressure drops, the line cd will repre- sent to some scale not here, determined the weight of a cubic foot at any discharge pressure Fig. 48. — Heat (Work) Available for Increasing Velocity. Since the product of the area through which the discharge takes place, the velocity and the weight per cubic foot of the 154 FLOW OF FLUIDS substance is equivalent to the weight in pounds of the substance discharged per second, the product of the ordinates at any point of the curves ab and cd is proportional to the weight discharged from a pressure of P\ to a condition where the pressure is P 2 . The line ceb represents this product. Evidently there is some low pressure into which the weight discharged per square foot will be a maximum, and this will be the pressure corresponding to the high point e on the curve. a V e \f v in.p ^ /4 d \ c & ^ f $? l/c b .2 .5 .6 .7 .9 1.0 Fig. 49. — Illustrative Curves of Weight, Discharge and Velocity. Weight per Cubic Foot. From the formula for adiabatic ex- pansion the weight per cubic foot can be obtained if the sub- stance is similar to air.* The general formula (applied to air) is (213) (214) * The exponent in the formula is the ratio of the specific heats (of air in this case). P^l-40 B P2^- 40 , q be reduced to 1 1 P 2 14 X Pi, t Pi 1 - 4 X RTi or -,- p 0.286 p 0.714 v 2 RTi FLOW OF AIR THROUGH AN ORIFICE 155 which is the weight in pounds per cubic foot of discharge. Pres- sures are in pounds per square foot. If the supply to the nozzle is from a large reservoir so that V± can be taken as zero then the discharge velocity is T 0.4 v, - V/Vx^Wx-g) v, = 109.6 \/ r, [1 - (0' 286 ]- (21s) All quantities on the right-hand side of this equation must be obtained from the data of tests. • Weight in pounds discharged through the area A (in square feet) is P 0.286 P„0-714 w = A x Fl Jj xi Kl 1 o 9 .6v/ r,[i - (0""} (216) Maximum Discharge. This weight is a maximum when — - = o or when P 2 = 0.525 Pi. The maximum quantity of air aP 2 will be discharged when the low pressure is 52.5 per cent of the high pressure. Shape of Nozzle. See page 167, on the flow of steam. Flow of Air through an Orifice. Air under comparatively high pressure is usually measured in practice by means of pressure and temperature observations made on the two sides of a sharp- edged orifice in a diaphragm. The method requires the use of two pressure gages on opposite sides of the orifice and a ther- mometer for obtaining the temperature ti at the initial or higher pressure pi. The flow of air w, in pounds per second, may then be calculated by Fliegner's formulas : w = 0.530 X f X a— t^z when pi is greater than 2 p 2 , (217) vTi w = 1.060 Xf X a 1 /P2 (Pi ~ P2) w hen p x is less than 2 p 2 , (218) V Ti 156 FLOW OF FLUIDS where a is the area of the orifice in square inches, f is a coeffi- cient, Ti is the absolute initial temperature in degrees Fahren- heit at the absolute pressure pi in the " reservoir or high-pressure side" and p 2 is the absolute discharge pressure, both in pounds per square inch. When the discharge from the orifice is directly into the atmosphere, p2 is obviously the barometric pressure. Westcott's and Weisbach's experiments show that the values of f are about 0.925 for equation (217) and about 0.63 for equa- tion (218). For small pressures it is often desirable to substitute manom- eters for pressure gages. One leg of a U-tube manometer can be connected to the high-pressure side of the orifice and the other leg to the low-pressure side. Valves or cocks are sometimes inserted between the manometer and the pipe in which the pressure is to be observed for the purpose of " dampening" oscillations. This practice is not to be recommended as there is always the possi- bility that the pressure is being throttled.* A better method is to use a U-tube made with a restricted area at the bend between the two legs. This will reduce oscillations and not affect the accuracy of the observations. Discharge from compressors and the air supply for gas engines are frequently obtained by orifice methods. When pi — p 2 is small compared with pi, the simple law of discharge f of fluids can be used as follows: * Report of Power Test Committee, Journal A. S.M.E., Nov., 191 2, page 1695. f If the density is fairly constant, 144 pi v£ 144 p 2 Vq2 s + 2g s i "2g' where Vi is the velocity in feet per second in the "approach" to the orifice, and v is the velocity in the orifice itself. Since Vi should be very small compared with v , Vq2 144 (p x - pa) 2g s ' Vo = V /: w 2 g X 144 (p x - p 2 ) . = favosa fas y ^^fo-p.) , FLOW OF AIR THROUGH AN ORIFICE 157 fa w = V 2 g X 144 (Pi - P2) s, (219) 144 where f is a coefficient from experiments, g is the acceleration due to gravity (32.2), and s is the unit weight of the gas meas- ured, in pounds per cubic foot, for the average of the initial and final conditions of temperature and pressure. If the difference in pressure is measured in inches of water h with a manometer, then 144 (pi — p 2 ) = — — X h (expressed in terms of pounds per square foot), w = y 2 ghs X — — (pounds per second), (220) 144 ^2 where 62.4 is the weight of a cubic foot of water (density) at usual "room" temperatures. This equation can also be transformed so that a table of the weight of air is not needed, since by elementary thermodynamics 144 pv = 53.3 T, where v is the volume in cubic feet of one pound and T is the absolute temperature in Fahrenheit. Since v is the reciprocal of s, then s = 144 p + 53.3 T, and w = 0.209 fa V/^ ( 221 ) Here p and T should be the values obtained by averaging the initial and final pressures and temperatures. Great care should be exercised in obtaining correct temperatures. For accurate work, corrections of s for humidity must be made.* For measurements made with orifices with a well-rounded entrance and a smooth bore so that there is practically no Con- or w = fa VsTg x 144 (pi — p 2 )s. Professor A. H. Westcott has computed from accurate experiments that the value of the coefficient f in these equations is approximately 0.60. * Tables of the weight of air are given on page 181 and tables of humidity on page 368 in Moyer's Power Plant Testing (2d Edition). 158 FLOW OF FLUIDS traction of the jet the coefficient f in equations (217) and (218) may be taken as 0.98. In the rounding portion of the entrance to such a nozzle the largest diameter must be at least twice the diameter of the smallest section. For circular orifices with sharp corners Professor Dalby * stated that the coefficient for his sharp-edged orifices in a thin plate of various sizes from 1 inch to 5 inches in diameter was in all cases approximately 0.60; and these data agree very well with those published by Durley.j When p 2 -J- pi = 0.99 the values obtained with this coefficient are in error less than J per cent; and when p 2 -f- pi = 0.93 the error is less than 2 per cent. Receiver Method of Measuring Air. None of the preceding methods are adaptable for measuring the volume of air at high pressures as in the case of measuring the discharge in tests of air compressors. Pumping air into a suitably strong receiver is a method often used. The compressor is made to pump against any desired pressure which is kept constant by a regu- lating valve on the discharge pipe: Pi and P 2 = absolute initial and final pressures for the test, pounds per square inch. Ti and T 2 = mean absolute initial and final temperatures, de- grees Fahrenheit. Wi and w 2 = initial and final weight of air in the receiver, pounds. V = volume of receiver, cubic feet. PiV = wRTi, and P 2 V = w 2 RT 2 , 'where R is the constant 53.3 for air, then weight of air pumped L (h _ h\ i.3 VT, Tj w 2 - wi = — - (—- — )• (222) In accurate laboratory tests the humidity of the air entering the compressor should be measured in order to reduce this * Engineering (London), Sept. 9, 19 10, page 380, and Ashcroft in Proc. Insti- tution of Civil Engineers, vol. 173, page 289. f Transactions American Society of Mechanical Engineers, vol. 27 (1905), page 193. FLOW OF VAPORS 159 weight of air to the corresponding equivalent volume at atmos- pheric pressure and temperature. The principal error in this method is due to difficulty in measur- ing the average temperature in the receiver. Whenever practi- cable the final pressure should be maintained in the receiver at the end of the test until the final temperature is fairly constant. Flow of Vapors. In Fig. 45 suppose the sections A and B are so proportioned that the velocity of the substance passing section A is the same as that at section B. Such a condition might arise in a calorimeter or in the expansion of ammonia through a throttling or expansion valve, as in an ice machine. The pressure at A will be Pi which is greater than the pressure at B of P 2 . Fig. 50 represents the entropy dia- gram for such a condition. As the pressure falls from Pi to P 2 the maxi- mum heat available to produce veloc- ity through the nozzle is the area acde. The value of the quality, rep- resented bv the symbol x for the substance after leaving the nozzle FlG ' S °'~ Q ^%^ T n ° Ve ~ corresponds to that of point c and the area acde is the excess kinetic energy represented by the increased velocity. This excess kinetic energy is destroyed by coming into contact with the more slowly moving particles at B and with the sides of the vessel. The area acde is equal to (h a + x a L a ) — (h c + x c L c ) and the relation of x a to x c is obvi- ously adiabatic. The area ohdbf equals area oheag (thus the heat content at b is the same as at a). The location of b can be found as follows: I 6 ' Pi a Id c b / *" h T-Ent.-Diagram 9 f Xb Ha ~T~ Xa-L*a »^& (223) The curve shown in Fig. 51 represents the discharge of a mix- ture of steam and water (x = 0.6 at 100 pounds per square inch absolute pressure) into a vessel having the pressures shown. The i6o FLOW OF FLUIDS points on this curve cannot be determined by entropy tables. At ioo pounds per square inch pressure the total heat of the wet steam is h + 0.6 L or 298.5 + 0.6 X 887.6 = 831. 1 B.t.u. per pound. 2.00 1.75 1.50 o a o o £ 1.25 o o 1 is ^ 1 1.00 ra 03 a .75 .50 .25 4/ to/ 7 10 20 30 40 50 60 70 80 90 100 Discharge Pressureln. lbs. per sq. in. Fig. 51. — Discharge of Steam Under Various Pressures. At 60 pounds per square inch absolute pressure the total heat may be found by the use of the entropy diagram shown in Fig. 52. The entropy values are taken directly from steam tables. The entropy for the initial point is, then, ab = 0.4748 + 0.6 X 1. 1273 = 1.1512. The distance dc = ab — 0.4279 = 0.7233, and x at 60 pounds is : dc 0.7233 = = 0.595. 1. 2154 1. 2154 The total heat at 60 pounds pressure is h + 0.595 L = 262 -4 + 0.595 X 914.3 = 805.4. FRICTION LOSS IN A NOZZLE 161 The velocity of flow is V2 x 32.2 x 778 (831. 1 — 805.4) = 1135 feet per second. The volume of one pound is 0.016 (1.0 — 0.595) + 7.166 X 0.595 = 4.27 cubic feet, and the weight per cubic foot is 4.27 = 0.2342 pound. 1.1273- 1.1512- 1.2154- T-Ent.-Diagram The weight discharged per square inch per second is 1135 X 0.2342 _ , — — ^- = 1. 8 s pounds. 144 F Velocity of Flow as Affected by Radiation. Fig. 53 shows the radia- ,..,.,....., tion losses. The condition at entrance tropy Diagram for Calculating is represented at a and the area acde the Weight of Discharge of represents the quantity of heat lost team * by radiation. Area aefg represents the velocity change while the point e represents, the condition of the moving substance. If, after passing through the nozzle, the velocity is reduced to that of en- trance, a point located as at b will represent the condition of the sub- stance. This point would be so located that area aefg . , x (224) T.- Ent.- Diagram eb = L f Friction Loss in a Nozzle. Fig. 54 shows the friction loss. The energy converted into heat by friction varies with the square of the velocity. In Fig. 53. — Diagram illustrating this figure, a is the initial condition Radiation Loss in Nozzle. and acfg ^ ^ energy available for change in velocity provided there is no frictional loss. The ratio of the areas acde to acfg is the proportional loss by friction. The point c represents the condition of the substance at the l62 FLOW OF FLUIDS return of the friction heat to the substance. The heat is returned in exactly the same way as if it came from an outside source. The distance ch is the area acde -T- L c . The area edfg represents the energy expended in the velocity change and the point h represents the state of the substance at the point of discharge. This condition is found existing in the fixed nozzle of most turbines. Point a represents the condition on the high-pressure side of the nozzle and point h, the low-pressure side. The absolute velocity of discharge is T.- Ent.- Diagram n I d a Fig. 54. — Diagram Illustrating really caused by the energy repre- Friction Loss in Nozzle. S ented by the area edfg. Impulse Nozzles. Suppose that the substance is discharged with an absolute velocity corresponding to the area edfg (Fig. 54), and that it passes into a mov- ing nozzle, having the same pressure on the discharge as on the intake side. The energy represented by the area edfg would be used up in the following ways: (1) by the fric- tion in moving nozzle; (2) residual absolute velocity; (3) and energy used in driving the moving nozzle against the resistance. Fig. 55 shows the quantities used up by each. Point a represents the condition of the substance before passing into the fixed nozzle while point h shows its condition leaving the fixed nozzle, the velocity corre- sponding to the area edfg. Area klde represents the energy used up in friction in the moving nozzle; area klnm residual T.- Ent.- Diagram Fig. 55. — Diagram of Heat Losses in a Steam Nozzle (Impulse). TURBINE LOSSES 163 velocity after leaving moving nozzle and area mnfg represents useful work used in moving the nozzle against its resistance. The condition of the substance leaving the nozzle is shown at q and not at h, the distance h r- q being the area edlk divided by Ln. The substance leaves the moving nozzle with a velocity corresponding to the area klnm and it will have done work corresponding to the area mnfg. Turbine Losses. Fig. 56 is a simple velocity diagram show- ing, for an impulse nozzle such as occurs in many turbines, the relative value of those various losses. A is a stationary nozzle e v Fig. 56. — Impulse Nozzle and Velocity Diagrams. discharging against the movable blades B. The path of the steam is shown by the dotted line. The line db marked v represents the velocity of discharge of the stationary nozzle, which makes an^angle a with the direction of motion of the moving blades. Call ev the velocity of the moving blades, then h is the amount and direction of the relative velocity of the steam over the surface of the moving blades. It loses a portion of this velocity as it passes over the surface of the blades and Ih becomes the actual relative velocity of discharge. The direction of Ih is de- termined by the discharge edge of the moving blades, the angles a and /3 being as shown. The residual absolute velocity is rep- resented by r. The total energy equivalent of the velocity developed in B.t.u. per pound = 2g (225) 164 FLOW OF FLUIDS w The residual energy per pound = — 2 i (226) n T.- Ent.- Diagram Reaction Nozzles. When the substance leaving the station- ary nozzle passes into a moving nozzle having the pressure at the intake greater than at the discharge, the conditions differ from those just discussed. The velocity in this case is changed in passing through the moving nozzle. In the equations given in the previous discussion it was assumed that the moving nozzles were entirely filled with the sub- stance, and when partly filled in the expanding portion, coefficients of correction were applied, but in this case the nozzles should be so de- signed that the substance entirely fills them, as the corrections are un- known. In Fig. 57 the lines of Fig. 55 are reproduced together with those re- lating directly to the reaction nozzle. Point a corresponds to the condition on entering the stationary nozzle, Fig. 57. -Diagram of Heat Losses •<. h ^ condition on leaving ft in a Steam Nozzle (Reaction). . with a velocity corresponding to the area edfg. Point k represents the pressure at the discharge end of the moving nozzle, and if no friction losses or impact loss occur in the moving nozzle, point k would represent the condition of the discharged substance and the area egmkhd would be accounted for as useful work done and residual velocity. But since friction losses and impact loss do occur a portion of this area edhkno can be set aside to represent these losses, a portion noqp represents the residual velocity, while the remaining area pqgm represents the useful work done. The condition of the substance leaving the moving nozzle is , , ,, ,. . , , 1 • area edhkno . given by k, the distance kl being Area onpq rep- Li resents the residual velocity. INJECTORS 165 Coefficient of Flow. Few experiments have been carried on for determining the flow of steam in nozzles proportioned for maxi- mum discharge. For a nozzle having a well rounded entrance and with the parallel portion of least diameter from 0.25 to 1.5 times the length of the converging entrance, the coefficient of discharge is about 1.05. For properly shaped entrances and for areas of orifices between 0.125 square inch and 0.75 square inch the coefficient of discharge varies from 0.94, the two pressures being nearly alike, to unity, the ratio of the pressures being 0.57. For an orifice through a thin plate the coefficient is about 0.82, the ratio of the pressures being 0.57. Injectors. In an injector, steam enters at A in Fig. 58 at the pressure of the supply. The quantity of water entering at C, the cross-section of the pipe, and the pressure of the water determine the pressure at B. At D the pressure should be zero (atmos- pheric) or equal to the pressure in the water supply pipe to which D Fig. 58. --Essential Parts of an may be connected. 'The total hy- draulic head should exist as velocity head at this point. At E the pressure should be sufficient to raise the check valve into the boiler and the velocity sufficient to carry the intended supply into the discharge pipe. The shape of the nozzle from A to B should be such as to con- vert the energy in the steam at A into velocity at B. At B the water and steam meet, condensing the steam, heating the water and giving to the water a velocity sufficient to carry it through the nozzle B-D. All the energy accounted for at A and C must be accounted for at E. The heat lost by radiation may be neglected. The veloc- ity at any section of the nozzle equals volume passing in cubic feet area of section in square feet or V A = — » where a = area at any section corresponding to velocity V and a a = area at section A . 1 66 FLOW OF FLUIDS Weight of Feed Water Supplied by an Injector per Pound of Steam. Assuming the steam supply to be dry the heat units contained in the steam and feed water per pound and the heat in the mixture of steam and feed water per pound may be easily calculated. Knowing the rise of temperature of the water passing through the injector and neglecting radiation losses, the pounds of feed water supplied per pound of steam used by the injector may be obtained. Thus : Heat units lost by steam = Kinetic energy of jet + Heat units gained by feed water. The kinetic energy of jet may be neglected since it is very small, then, H — h/ = w (km — hf) H -h f , v W = =-> (227) rim — hf where w = the weight of feed water lifted per pound of steam. h m = heat of liquid of mixture of condensed steam and feed water. hf = heat of liquid of entering feed water. Thermal Efficiency of Injector. The thermal efficiency of an injector neglecting radiation losses is unity. All the heat ex- pended is restored either as work done or in heat returned to the boiler. Mechanical Efficiency of Injector. The mechanical work per- formed by the injector consists in lifting the weight of feed water and delivering it into the boiler against the internal pressure. The efficiency, considering the injector as a pump, is Work done B.t.u. given up by steam to perform the work or where U = [wl s + (w + 1) l P ] -f- 778 (in heat units). FLOW OF STEAM THROUGH NOZZLES 167 Is = W = pressure head corresponding to boiler gage pressure, in feet, suction head in feet, pounds of water delivered per pound of steam. Orifice Measurements of the flow of steam are sometimes used for ascertaining the steam consumption of the "auxiliaries" in a power plant. This method commends itself particularly because of its simplicity and accuracy. It is best applied by inserting a plate § inch thick with an orifice one inch in diameter, with square edges, at its center, between the two halves of a pair of flanges on the pipe through which the steam passes. Accurately cali- brated steam gages are required on each side of the orifice to determine the loss of pressure. The weight of steam for the various differences of pressure may be determined by arranging the apparatus so that the steam passing through the orifice will be discharged into a tank of water placed on a platform scales. The flow through this orifice in pounds of dry saturated steam per hour when the discharge pressure at the orifice is 100 pounds by the gage is given by the following table: Pressure drop, lbs. per sq. in. Flow of dry steam per hour, lbs. Pressure drop, lbs. per sq. in. Flow of dry steam per hour, lbs. 1 2 I 2 3 4 430 6i5 930 1200 1400 5 10 15 20 1560 2180 2640 3050 Flow of Steam through Nozzles. The weight of steam dis- charged through any well-designed nozzle with a rounded inlet, similar to those illustrated in Figs. 59 and 60, depends only on the initial absolute pressure (Pi), if the pressure against which the nozzle discharges (P 2 ) does not exceed 0.58 of the initial pressure. This important statement is well illustrated by the following example. If steam at an initial pressure (Pi) of 100 pounds per square inch absolute is discharged from a nozzle, the i68 FLOW OF FLUIDS weight of steam flowing in a given time is practically the same for all values of the pressure against which the steam is dis- charged (P 2 ), which are equal to or less than 58 pounds per square inch absolute. If, however, the final pressure is more than 0.58 of the initial, the weight of steam discharged will be less, nearly in proportion as the difference between the initial and final pressures is re- duced. The most satisfactory and accurate formula for the " constant flow " con- dition, meaning when the final pressure is 0.58 of the initial pressure or less, is the following, due to Grashof,* where w is the flow of steam f (initially dry saturated) in pounds per second, A Q is the area of the smallest section of the nozzle in square inches, and Pi is the initial abso- lute pressure of the steam in pounds per square inch, Fig. 59. — Example of a Well- designed Nozzle. or, in terms of the area, w = A, = ApPj 60 60 w 97 Pi 97 (229) (230) * Grashof, Theoretische Maschinenlehre, vol. 1, iii; Hiitte Taschenbuch, vol. 1, page 2>2>Z- Grashof states the formula, w = 0.01654 A oPr 9696 , but the formula given in equation (229) is accurate enough for all practical uses. t Napier's formula is very commonly used and is accurate enough for most calculations. It is usually stated in the form w = 70 where w, Pi, and Ao have the same significance as in Grashof s formula. The following formula is given by Rateau, but is too complicated for convenient use: w = 0.001 A0P1 [15.26 — 0.96 (log Pi + log 0.0703)]. Common or base 10 logarithms are to be used in this formula. FLOW OF STEAM THROUGH NOZZLES 169 These formulas are for the flow of steam initially dry and saturated. An illustration of their applications is given by the following practical example. Example. The area of the smallest section (A ) of a suitably designed nozzle is 0.54 square inch. What is the weight of the DeLaval Type. Nozzle* Diaphragm, Curtis Type. Fig. 60. — Examples of Standard Designs of Nozzles. flow (w) of dry saturated steam per second from this nozzle when the initial pressure (Pi) is 135 pounds per square inch absolute and the discharge pressure (P 2 ) is 15 pounds per square inch ab- solute? Here P 2 is less than 0.58 Pi and Grashof's formula is applicable, 170 FLOW OF FLUIDS O.54 (l3$) -97 or, w = D ^ ) OJ/ > 60 0.54 X 1 16.5* , , w = __^z — ^l_ = L040 pounds per second. 60 When steam passes through a series of nozzles one after the other as is the case in many types of turbines, the pressure is reduced and the steam is condensed in each nozzle so that it becomes more moist each time. In the low-pressure nozzles of a turbine, therefore, the steam may be very wet although initially it was dry. Turbines are also sometimes designed to operate with steam which is initially wet, and this is usually the case when low-pressure steam turbines are operated with the exhaust from non-condensing reciprocating engines. In all these cases the nozzle area must be corrected for the moisture in the steam. For a given nozzle the weight discharged is greater for wet than for dry steam; but the percentage increase in the discharge is not nearly in proportion to the percentage of mois- ture as is often stated. The general equation for the theoretic discharge (w) from a nozzle" is in the form f * The flow (w) calculated by Napier's formula for this example is w = -^ — 70 = 1. 04 1 pounds per second. f The general equation for the theoretic flow is / r 2 g+1 -1 where the symbols w, A , Pi, and g are used as in equations (228) and (229). P 2 is the pressure at any section of the nozzle, vi is the volume of a pound of steam at the pressure Pi, and k is a constant. The flow, w, has its maximum value when 2 i-fl I m-m is a maximum. Differentiating and equating the first differential to zero gives 1 il = ( 2 V" 1 Pi U + i/ ' P 2 is now the pressure at the smallest section, and writing for .clearness P for P 2 , and substituting this last equation in the formula for flow (w) above, we have FLOW OF STEAM 1 71 fp w = K K /—, (231) where Pi is the initial absolute pressure and Vi is the specific vol- ume (cubic feet in a pound of steam at the pressure Pi). Now, neglecting the volume of the water in wet steam, which is a usual approximation, the volume of a pound of steam is proportional to the quality (xi). For wet steam the equation above becomes then (232) The equation shows, therefore, that the flow of wet steam is inversely proportional to the square root of the quality (xi). Grashof's equations can be stated then more generally as w = ^r_ <*»> . 60 W A / V = _ p^ — (234) These equations become the same as (229) and (230) for the case where X\ = 1. Flow of Steam when the Final Pressure is more than 0.58 of the Initial Pressure. For this case the discharge depends upon the final pressure as well as upon the initial. No satisfactory formula can be given in simple terms, and the flow is most easily calculated with the aid of the curve in Fig. 61, due to Rateau. -Wm?M Now regardless of what the final pressure may be, the pressure (P ) at the smallest section of a nozzle (Aq) is always nearly 0.58 Pi for dry saturated steam. Making then in the last equation P = 0.58 Pi and putting for k Zeuner's value of 1.135 for dry saturated steam, we may write in general terms the form stated above, V Vi where K is another constant. See Zeuner's Theorie der Turbinen, page 268 (Ed. of 1899)- 172 FLOW OF FLUIDS This curve is used by determining first the ratio of the final to p the initial pressure — -, and reading from -the curve the corre- sponding coefficient showing the ratio of the required discharge to that calculated for the given conditions by either of the equa- tions (229) or (233). The coefficient from the curve times the 1.0 1 1 — ' _ qT ,9 lC I- .8 S§' 7 1 1- 6 * * ja <3 .5 -? +3 CO § £ A ^ 2 & a <3 n © r° .3 O PH *° .2 i :o uo .8 .7 «£ Batio of FfnaT to Initial PressureJ^L , Pi .5 Fig. 61. — Coefficients of the Discharge of Steam when the Final Pressure is Greater than 0.58 of the Initial Pressure. flow calculated from equations (229) or (233) is the required re- sult. Obviously the discharge for this condition is always less than the discharge when the final pressure is equal to or less than 0.58 of the initial. Length for Nozzles. The length of the nozzle is usually made to depend only on the initial pressure. In other words, the length of a nozzle for 150 pounds per square inch initial pressure is usually made the same for a given type regardless of the final pressure. And if it happens that there is crowding for space, one or more of the nozzles may be made a little shorter than the others. UNDER- AND OVER-EXPANSION m Designers of De Laval nozzles follow practically the same " elastic " method. The divergence of the walls of non-con- densing nozzles is about 3 degrees from the axis of the nozzle, and condensing nozzles for high vacuums may have a divergence of as much as 6 degrees * for the normal rated pressures of the turbine. One of the authors has used successfully the following empirical formula to determine a suitable length, L, of the nozzle between the throat and the mouth (in inches) : L = V I5 A Q j (235) where A is the area at the throat in square inches. Under- and Over-expansion. The best efficiency of a nozzle is obtained when the expansion required is that for which the nozzle ao $0 P « ° '» & o * « I So .2 « 1*2 * — r+- / / 1 1 1 i 1 i 1 -4- 30 25 20 15 10 ^ 5 "Percentage Nozzle is too Small^ at Mouth (Under Expansion) 5 10 15 20 25 30 Percentage Nozzle is too Larger at Month (Over Expansion) Fig. 62. — Curve of Nozzle Velocity Loss. was designed, or when the expansion ratio for the condition of the steam corresponds with the ratio of the areas of the mouth and throat of the nozzle. A little under-expansion is far better, however, than the same amount of over-expansion, meaning that a nozzle that is too small for the required expansion is more * According to Dr. O. Recke, if the total divergence of a nozzle is more than 6 degrees, eddies will begin to form in the jet. There is no doubt that a too rapid divergence produces a velocity loss. f Moyer's Steam Turbines. 174 FLOW OF FLUIDS efficient than one that is correspondingly too large.* Fig. 62 shows a curve representing average values of nozzle loss | used to determine discharge velocities from nozzles under the condi- tions of under- or over-expansion. Non-expanding Nozzles. All the nozzles of Rateau steam turbines and usually also those of the low-pressure stages of Curtis turbines are made non-expanding; meaning, that they have the same area at the throat as at the mouth. For such conditions it has been suggested that instead of a series of separate nozzles in a row a single long nozzle might be used of which the sides .*-■*! 1(U9 J6.19£H Fig. 63. — Non-expanding Nozzles. were arcs of circles corresponding to the inside and outside pitch diameters of the blades. Advantages would be secured both on account of cheapness of construction and because a large amount of friction against the sides of nozzles would be eliminated by omitting a number of nozzle walls. Such a construction has not proved desirable, because by this method no well-formed jets are secured and the loss from eddies is excessive. The general statement may be made that the throat of a well-designed nozzle should have a nearly symmetrical shape, as for example a circle, a square, etc., rather than such shapes as ellipses and long rect- * It is a very good method to design nozzles so that at the rated capacity the nozzles under-expand at least 10 per cent, and maybe 20 per cent. The loss for these conditions is insignificant, and the nozzles can be run for a large overload (with increased pressures) in nearly all types without immediately reducing the efficiency very much. f C. P. Steinmetz, Proc. Am. Soc. Mech. Engineers, May, 1908, page 628; J. A. Moyer, Steam Turbines. MATERIALS FOR NOZZLES 1 75 angles. The shape of the mouth is not important. In Curtis turbines an approximately rectangular mouth is used because the nozzles are placed close together (usually in a nozzle plate like Fig. 60) in order to produce a continuous band of steam; and, of course, by using a section that is rectangular rather than circular or elliptical, a band of steam of more nearly uniform velocity and density is secured. Fig. 63 shows a number of designs of non-expanding nozzles used by Professor Rateau. The length of such nozzles beyond the throat is practically negligible. Curtis non-expanding noz- zles are usually made the same length as if expanding and the length is determined by the throat area. Materials for Nozzles. Nozzles for saturated or slightly super- heated steam are usually made of bronze. Gun metal, zinc alloys, and delta metal are also frequently used. All these metals have unusual resistance for erosion or corrosion from the use of wet steam. Because of this property as well as for the reason that they are easily worked with hand tools * they are very suitable materials for the manufacture of steam turbine nozzles. Superheated steam, however, rapidly erodes all these alloys and also greatly reduces the tensile strength. For nozzles to be used with highly superheated steam, cast iron is generally used, and except that it corrodes so readily is a very satisfactory material. Commercial copper (about 98 per cent) is said to have been used with a fair degree of success with high super- heats; but for such conditions its tensile strength is very low. Steel and cupro-nickel (8 Cu + 2 Ni) are also suitable materials, and the latter has the advantage of being practically non-cor- rodible. The most important part of the design of a nozzle is the deter- mination of the areas of the various sections — especially the smallest section, if the nozzle is of an expanding or diverging type. In order to calculate the areas of nozzles we must know how to determine the quantity of steam (flow) per unit of time passing through a unit area. It is very essential that the * Nozzles of irregular shapes are usually filed by hand to the exact size. 176 FLOW OF FLUIDS nozzle is well rounded on the " entrance " side and that sharp edges along the path of the steam are avoided. Otherwise it is not important whether the shape of the section is circular, elliptical, or rectangular with rounded corners. Whether the nozzle section is throughout circular, square, or rectangular (if these last sections have rounded corners) the efficiency as measured by the velocity will be about 96 to 97 per cent, corresponding to an equivalent energy efficiency of 92 to 94 per cent. PROBLEMS 1. Air at a temperature of ioo° F. and pressure of 100 lbs. per sq. in. ab- solute flows through a nozzle against a back pressure of 20 lbs. per sq. in. absolute. Assuming the initial velocity to be zero, what will be the ve- locity of discharge? 2. If the area at the mouth of the above nozzle is 0.0025 sq. ft. and the coefficient of discharge is unity, how many pounds of air will be discharged per minute? 3. What will be the theoretical kinetic energy per minute of the above jet assuming no frictional losses? 4. Steam at a pressure of 150 lbs. per sq. in. absolute and 3 per cent moisture flows through a nozzle against a back pressure of 17 lbs. per sq. in. absolute. Calculate the velocity at the throat of the nozzle. What will be the velocity at the end of the nozzle? 5. Steam at a pressure of 200 lbs. per sq. in. absolute, temperature 530 F., expands in a nozzle to a vacuum of 28.5 ins. (30-in. barometer). Calculate the absolute velocity of the steam leaving the nozzle. 6. The area of a nozzle at its smallest section is 0.75 sq. in. It is sup- plied with dry saturated steam at 160 lbs. per sq. in. absolute pressure and the exhaust pressure is 2 lbs. per sq. in. absolute. How many pounds of steam per hour will the nozzle discharge? 7. A steam nozzle is to be designed that will discharge 500 lbs. of steam per hour. The pressure of the steam is 175 lbs. per sq. in. absolute and has ioo° F. superheat. The exhaust pressure is 28 ins. vacuum (barometer 29.82). What will be the area of the nozzle at its smallest section and at its end? 8. A safety valve is to be designed for a 200 horse power boiler generating steam at 150 lbs. per sq. in. absolute pressure and 5 per cent moisture. Assuming that the safety valve should have a capacity such that it will release the boiler of all steam when generating double its rated capacity, what will be the smallest sectional area of the valve? PROBLEMS 177 9. An injector supplies water to a boiler. The boiler pressure is 100 lbs. per sq. in. absolute and the steam generated is dry and saturated, the tem- perature of the entering feed water is 6o° F. and the temperature of the dis- charged mixture of condensed steam and feed water is 180 F. The suction head is 3 ft. What is the weight of feed water supplied to the boiler per pound of steam? What is the mechanical efficiency of the injector? 10. Design a nozzle to deliver 400 lbs. of steam per hour, initial pressure 175 lbs. per sq. in. absolute, final pressure atmospheric (barometer 28.62 ins.), temperature of steam 6oo° F. CHAPTER X APPLICATIONS OF THERMODYNAMICS TO COMPRESSED AIR AND REFRIGERATING MACHINERY COMPRESSED AIR Air when compressed may be used as the working medium in an engine, in exactly the same way as steam. Furthermore, it is an agent for the transmission of power and can be distributed very easily from a central station for the purpose of driving engines, operating quarry drills and various other pneumatic tools. Air Compressors. The type of machine used for the compres- sion of air is that known as a piston-compressor and consists of a cylinder provided with valves and a piston. The work performed in the air-cylinder of a compressor can best be studied successfully from an indicator diagram. If the compression is performed very slowly in a conducting cylinder, so that the air within may lose heat by conduction to the atmos- phere as fast as heat is generated by compression, the process will in that case be isothermal, at the temperature of the atmos- phere. Also if the compressed air is distributed to be used in compressed air motors * or engines without a change of temper- ature, and that the process of expansion in the compressed air motors or engines is also indefinitely slow and consequently isothermal, then (if we neglect the losses caused by friction in pipes) there would be no waste of power in the whole process of transmission. The indicator diagram would then be the same per pound of air in the compressor as in the air motor or engine, although the course of the cycle would be the reverse — that is, it would retrace itself. * Compressed air motors are similar to steam engines, but use compressed air instead of steam. 178 WORK OF COMPRESSION 179 Adiabatic compression and expansion take place approximately if the expansion and compression are performed very quickly, or when the air is not cooled during compression, — in such a case the temperature of the air would rise. The theoretical indicator diagram of the compressor, Fig. 64, is FCBE and that 3Y Volume Fig. 64. — Diagram of Compressor. Volume Fig. 65. — Diagram of Air Engine. of the air engine, Fig. 65, is EADF. CB and AD are both adiabatic lines. The change of volume of the compressed air from that of EB to EA occurs through its cooling in the dis- tributing pipes, from the temperature produced by adiabatic compression down to the temperature of the atmosphere. Suppose both diagrams of the compressor and of the air engine are superimposed as in Fig. 66, and then an imaginary isothermal line is drawn between the points A and C. P D Volume FlG. 66. — Superimposed Diagrams of Figs. 21 and 22. It is then evident that the use of adiabatic compression causes a waste of power which is measured by the area ABC, while the use of the adiabatic expansion in the air engine involves a further waste, shown by the area ACD. Work of Compression. Assuming no clearance in the com- pressor and isothermal compression, the pressure-volume diagram will be similar to Fig. 64. The work of the cycle will be l8o COMPRESSED AIR AND REFRIGERATING MACHINERY W = PcVc ~ PcVdoge^ V b PbV bV b, which becomes, since P C V, W = P b V b , Vc Vb \ -PcVAoge^. V c (236) (237) In practice the compression cannot be made strictly isother- mal, as the operation of the piston would be too slow. The dif- ference between isothermal and adiabatic compression (and ex- pansion) can be shown graphically as in Figs. 67 and 68. In Volume Fig. 67. — Compression Diagram. Volume Fig. 68. — Expansion Diagram. these illustrations the terminal points are correctly placed for a certain ratio for both compression and expansion. Note that in the compressing diagram (Fig. 67) the area between the two curves, ABC, represents the work lost in compressing due to heat- ing, and the area between the two curves, ACMNF (in Fig. 68), shows the work lost by cooling during the expansion. The isothermal curve AC will be the same for both cases. The temperature of the air is prevented as far as possible from rising during the compression by injecting water into the compressing cylinder, and in this way the compression curve will change. The curves which would have been PV = a constant, if isothermal, and PV 14 = a constant, if adiabatic, will be very much modified. In perfectly adiabatic conditions the exponent u n" = 1 .40 for air, but in practice the compressor cylinders are water- jacketed, and thereby part of the heat of compression is con- ducted away, so that " n" becomes less than 1.40. This value of " n" varies with conditions; generally the value is between 1.2 and 1.3. EFFECT OF CLEARANCE UPON VOLUMETRIC EFFICIENCY 181 When the compression curve follows the law, PV n equals a constant, work of compression (Fig. 64) is w = p c v c + PcVc ~ PbVb - P b V b n — 1 (PcVc - P b V b ), (238) n — 1 1 since P C V» = P»V»*; V b = V c (Q" (239) Combining equations (238) and (239), W-^P.V.[i-[^) J- (240) The Effect of Clearance upon Volumetric Efficiency. It is impossible to construct a compressor without clearance, con- sequently the indicator diagram differs from the ideal case. At the end of the discharge stroke, the clearance volume is rilled with compressed air. When the piston moves on its outward stroke, the clearance air expands and the suction valves of the compres- sor will be held shut until the piston has moved a sufficient dis- tance to permit the entrapped air to expand to atmospheric pressure. When that point is reached any further movement of the piston opens the suction valves and external air is drawn into the cylinder. Thus the entire stroke of the compressor piston is not effective in pumping air. The ratio of the volume of air pumped to the volume swept by the piston, or piston displace- ment of the cylinder, is termed volumetric efficiency. Fig. 69 illustrates an ideal compressor diagram with clearance. The air entrapped in the clearance space equals v 3 = CV S , where V s = volume swept or piston displacement of the cylinder. C = percentage of clearance. The air in Fig. 69 expands to F 4 at which point the inlet valves open. The air drawn into the cylinder is represented by the 182 COMPRESSED AIR AND REFRIGERATING MACHINERY difference in volume between Vi and F 4 . This air, as well as the clearance air, is compressed to point 2, while the compressed air is discharged from points 2 to 3. Knowing the per cent of clear- ex, v 3 =cy s L I 3 ft a\ i\ 1 \ 1 ^ 1 1 1 1 1 1 v% \4 \w ^^-— _ 1 i< 1 — 1 u v* 1 1 \f 1 t J f*— v s 1 Volume Fig. 69. — Ideal Air Compressor with Clearance. ance, the volume swept by the piston (V s ), and the initial and final pressure, the volumetric efficiency (Vet) may be deter- mined from the following equations: P% (CV s ) n = PiVi". 1 V* = (£)CV S , since V x = V s + CV S , V 1 - V, = V s + CV S -®y CV S i\ -1 i + Cii - p s v V s . TWO STAGE COMPRESSION 183 Therefore volumetric efficiency is Vet. = V s = i+C 1-1 i-m (241) The volumetric efficiency also decreases with the altitude, as the weight of a cubic foot of air decreases as the altitude increases. Two Stage Compression. The problem of economy, obviously,' becomes one of abstracting the heat generated in the air during the process of compression. As previously mentioned, this is partially accomplished by water-jacketing the cylinders, and also by water injection. Nevertheless, owing to the short interval within which the compression takes place, and the comparatively small volume of air actually in contact with the cylinder walls, very little cooling really occurs. The practical impossibility of proper cooling to prevent waste of energy leads to the alternative of discharging air from one cylinder after partial compression has been effected, into a so-called inter-cooler, intended to absorb the heat generated during the first compression, and then compressing the air to the final pressure in another cylinder. Volume Fig. 70. — Indicator Diagram of Two-stage Air Compressor. This operation is termed " two-stage " compression and when repeated one or more times for high pressures the term " multi- stage " compression applies. Referring to Fig. 70 and assuming the compression in a two- stage compressor to be adiabatic for each cylinder, the compres- 184 COMPRESSED AIR AND REFRIGERATING MACHINERY sion curve is represented by the broken line ABDE ; the compres- sion proceeds adiabatically in the first or low-pressure cylinder to B; the air is then taken to a cooler and cooled under practi- cally constant pressure until its initial temperature is almost reached, and its volume reduced from HB to HD; it is then introduced to the second or high-pressure cylinder and com- pressed adiabatically along the line DE to the final pressure condition that was desired. It is seen that the compression curve approaches the isothermal line FA.* The isothermal con- dition is obviously desired and, in consequence, air-machines are built to approach that condition as nearly as possible. Referring to Fig. 70, the work of each stage from equation (240) will be W (1st stage) = W (2d stage) n n — n r p °4 - ffi) " )• The total work of compression is W (total) = W (1st stage) + W (2d stage) n n PaVa 1—^7- n—V + PaV c B-n ©' With perfect cooling P a V a = P d V a ; also P 6 = P d ; P c = Pe, then n— 1 / n— 1\ "" W (total) n n -PaVa Cold Low Pressure Air Warmed Low Pressure Air / " \ V 1 < B - • 1 ' Brine Tank 1 ~ " j* [Circulating Brine] Warm i Pipes \lcold j jBrine Brine Fig. 72. — Dense Air System of Refrigeration. system, because a compressor is used to raise the pressure of the vapor and deliver it to the condenser after removing it from the evaporator. (C) The absorption system, using ammonia, and so-called be- THE AIR SYSTEM OF REFRIGERATION 189 cause a weak water solution removes vapor from the evaporator by absorption, the richer aqua ammonia so formed being pumped into a high-pressure chamber called a generator in communica- tion with the condenser, where the ammonia is discharged from the liquid solution to the condenser by heating the generator, to which the solution is delivered by the pump. No matter what system is used, circulating water is employed to receive the heat, the temperature of which limits the highest temperature allowable in the system and indirectly the highest pressure. The Air System of Refrigeration. The dense or closed air system is illustrated in Fig. 72, in which air, previously freed of moisture, is continuously circulated. The engine cylinder E furnishes power * to drive the compressor cylinder F. This cylinder delivers hot-compressed air into a cooler A where it is cooled, and then passed on to the expansion cylinder G (tan- dem-connected to both, the compressor F and to the engine cylinder E), which in turn sends cold low-pressure air first through the refrigerating coils in the brine tank B and then back to the compressor cylin- der F; thus the air cycle is completed. The courses of the circulating water and also of the brine are shown by the dotted lines. The dense-air cycle in a pressure- volume Fig. 73. — Pressure- vol- diagram is represented in Fig. 73, in which um e Diagram of Dense Air BC is the delivered volume of hot-corn- Cycle of Ref ^re- pressed air; CM is the volume of cooled air admitted in the ex- pansion cylinder; MB the reduction in volume due to the water cooler; MN the expansion; NA the refrigeration or heating of the air by the brme, and AB the compression. This operation is but a reproduction of that previously described. The work W c expended in the compression cylinder F is DABC * Since the work done by the expansion of the cool-compressed air is less than that necessary for the compressing of the air taken from the brine coils through the same pressure conditions, a means must be employed to make up for the dif- ference, and for this purpose the engine cylinder is used. 190 COMPRESSED AIR AND REFRIGERATING MACHINERY (Fig. 73) ; that done by the expansion cylinder G is W e = DCMN. The shaded area MB AN represents the work which must be sup- plied by the engine E. If w pounds of air are passing through the refrigerating machine per minute, the heat withdrawn from the cold room or absorbed by the brine along NA (Fig. 73) is Qna = wC P (t a — h). (245) The work expended in compressing w pounds of air, assuming poly tropic compression, is, by equation (240), If the compression is adiabatic, W c =wP a Va-^ L - 7 - I since -=?- = ( — ) v also AR = C v — C v = C v I- J If the expansion is complete in the expansion cylinder, the work done in expansion is We=^(t m '-h). (247) The net work of the engine E required to produce refrigeration becomes W = Wc - We = ^ (h ~ t a - t m + *„). (248) Since, from equation (245), w = -77^ (ta — t n ), equation (248) becomes l/*& ~~ ta — tm ~j~ tn\ \ t a -t n / 7—7 \/NA[tb — t a — tm ~T t n \ W = j-( : — ; ) * ( 2 49) THE VAPOR COMPRESSION SYSTEM OF REFRIGERATION 1 91 The Vapor Compression System of Refrigeration. The com- pression system for ammonia or similar condensable vapors is shown in Fig. 74. The figure illustrates the essential mem- bers of a complete compression refrigerating system. B repre- High Pres-> ' Bure Liquid R Ammonia Receiver Circulating Y Water I w Condenser <■ ->- High Pres- Asure Vapor Compressor Cylinder E Engine Cylinder Throttling or Expansion Valve Low Pressure Liquid Low Pres- sure Vapor t= — Circulating Brine- J Pipes I Warm f \ Cold Brine I j Brine Fig. 74. — Compression System of Refrigeration. sents the direct-expansion coil in which the working medium is evaporated; F, the compressor or pump, for increasing the pres- sure of the gasified ammonia; E, the engine cylinder, — the source of power; W, the condenser, for cooling and liquefying the gasi- fied ammonia; and V, a throttling valve, by which the flow of 192 COMPRESSED AIR AND REFRIGERATING MACHINERY liquefied ammonia under the condenser pressure is controlled as it flows from the receiver R to the expansion coils; B, the brine tank, in which a materially lower pressure is maintained by the pump or compressor in order that the working medium may boil at a sufficiently low temperature to take heat from and con- sequently refrigerate the brine which is already cooled. The operation of the compressor F (Fig. 74) is theoretically a reversed Rankine cycle (Figs. 31 and 32). If one pound of vapor is passed through the system, the work (Wc) of the compressor is W c = (#2 - #1) (B.t.u.), where Hi = the total heat of the vapor at entrance to the com- pressor, H 2 = the total heat of the vapor discharged from the com- pressor. The vapor entering the compressor may be treated as though it were dry and saturated. The entropy-temperature diagram (Fig. 75) illustrates this case. The vapor discharged by the compressor will then be superheated, having a temperature t s at a pressure P 2 . The condition of the discharged vapor is determined by equating the entropies at the inlet and discharge pressures. The total heat (H 2 ) of the discharged vapor will be H 2 = [fa + L 2 + C P (t s - k)]. (250) The horse power of the compressor is, if w pounds of vapor is circulated per minute: _ ^-#0 778, ( j 33,000 The heat absorbed per minute by w pounds of vapor passing through the refrigerating or brine coils will be Q r = w (fa + Li - fa) = w (Hi - fa). (252) fa = the liquid heat of the vapor after leaving the condenser. THE VAPOR ABSORPTION SYSTEM OF REFRIGERATION 193 The heat absorbed per minute by the condenser (Q c ) is w (H 2 - ho) (B.t.u.). (253) The heat absorbed by the condenser is theoretically equal to the sum of the heat absorbed in the refrigerator and the heat equivalent of the work of compression. Ammonia compressors are operated either on the dry or on the wet system. In the dry system the ammonia entering the compressor is a dry vapor as illustrated in Fig. 75. In the wet system the ammonia enters the compressor in the wet state, the heat developed during the com- pression being used in evapo- rating the liquid ammonia into a vapor. The Vapor Absorption Sys- tem of Refrigeration. The ab- sorption system depends upon the fact that anhydrous am- monia possesses the property of forming aqua ammonia. The amount of ammonia water will absorb depends upon the temperature of the water; the colder the water, the greater are its absorptive powers. The absorption system differs from the vapor compression system in that the absorption system replaces the compressor by an absorber, where the anhydrous ammonia is changed into aqua ammonia, a pump which transfers the ammonia from the absorber to the generator, and a generator, where the aqua ammonia is heated. Both systems have a condenser where the ammonia is cooled and liquefied and an expansion valve or throttling valve by means of which the flow of liquid ammonia to the expansion coils is controlled. In the absorption system the anhydrous ammonia vapor flows from the expansion coils to T 2 T/' / p 2 y / , \ Si S a £ H Fig. 75. Entropy -0 — Entropy -Temperature Dia- gram for Ammonia. 194 COMPRESSED AIR AND REFRIGERATING MACHINERY the absorber, in which the anhydrous vapor comes in contact with weak aqua ammonia. The weak ammonia absorbs the ammonia vapor. From the absorber the ammonia is pumped into the generator, where it is heated by steam coils. The vapor driven off in the generator passes to the condenser and from there through the expansion or throttle valve to the expansion coils which are located in the brine tank or in the refrigerating room. The absorption system is usually provided with a rectifier to thoroughly dry the gas before it enters the condenser, an ex- changer which heats the strong ammonia by cooling the weak ammonia, and with other auxiliary equipment to reduce the heat losses in the system. COEFFICIENT OF PERFORMANCE OF REFRIGERATING MACHINES The Coefficient of Per- 1 ___ Heat extracted from the cold body formance j" Work expended This ratio may be taken as a coefficient of performance in esti- mating the merits of a refrigerating machine. When the limits of temperature 2\ and T 2 are assigned it is very easy to show by a slight variation of the argument used in Chapter IV that no refrigerating machine can have a higher coefficient of performance than one. which is reversible according to the Carnot method. For let a refrigerating machine S be driven by another R which is reversible and is used as a heat-engine in driving S. Then if S had a higher coefficient of performance than R it would take from the cold body more heat than R (working reversed) rejects to the cold body, and hence the double machine, although purely self-acting, would go on extracting heat from the cold body in violation of the Second Law of Thermodynamics. Reversi- bility, then, is the test of perfection in a refrigerating machine just as it is in a heat-engine. When a reversible refrigerating machine takes in all its heat, namely Q c at T 2j and rejects all, namely Q a at T\, and if we repre- sent the heat equivalent of the work done by W = Q a — Qc, then the coefficient of performance is, as already denned, PROBLEMS 195 Qc _ Qc T 2 W Qa-Qc ZV-T, (254) Hence, the smaller the range of temperature, the better is the performance. To cool a large mass of any substance through a few degrees will require much less expenditure of energy than to cool one-fifth of the mass through five times as many degrees, although the amount of heat extracted is the same in both cases. If we wish to cool a large quantity of a substance it is better to do this by the direct action of a refrigerating machine working through the desired range of temperature, than to cool a portion through a wider range and then let this mix with the rest. This is only another instance of a wide, general principle, that any mixture of substances at different temperatures is ther- modynamically wasteful because the interchange of heat between them is irreversible. An ice-making machine, for example, should have its lower limit of temperature only so much lower than 3 2 F. as will allow heat to be conducted to the working fluid with sufficient rapidity from the water that is to be frozen. PROBLEMS 1. If 200 cu. ft. of free air per minute (sea-level) is compressed isother- mally and then delivered into a receiver, the internal pressure of which is 102.9 lbs. per sq. in. absolute, find the theoretical horse power required. 2. What will be the net work done in foot-pounds per stroke by an air compressor displacing 3 cu. ft. per stroke and compressing air from atmos- pheric pressure to a gage pressure of 75 lbs.? (Isothermal compression.) 3. What horse power will be needed to compress adiabatically 1500 cu. ft. of free air per minute to a gage pressure of 58.8 lbs., when n equals 4. A compressed-air motor without clearance takes air at a condition of 200 lbs. per sq. in. (gage) and operates under a cut-off at one-fourth stroke. What is the work in foot-pounds that can be obtained per cubic foot of compressed air, assuming free air pressure of 14.5 lbs. and n equal to 1 .41? 5. Find the theoretical horse power developed by 3 cu. ft. of air per minute having a pressure of 200 lbs. per sq. in. absolute, if it is admitted and expanded in an air engine with one-fourth cut-off. The value of n is 1.2. (Neglect clearance.) 196 COMPRESSED AIR AND REFRIGERATING MACHINERY 6. Compute the net saving in energy that is effected by compressing isothermally instead of adiabatically 50 cu. ft. of free air to a pressure of 200 lbs. per sq. in. gage. Barometer = 14 lbs. per sq. in., and a tempera- ture of 70 F. What is the increase in intrinsic energy during each kind of compression? How much heat is lost to the jacket-water during each kind of compression? 7. Let a volume of 12 cu. ft. of free air be adiabatically compressed in a one stage air compressor from atmospheric pressure (15 lbs.) to 85 lbs. gage; the initial temperature of the air being 70 F. (a) What is the volume and temperature of the air after the com- pression? (b) Suppose this heated and compressed air is cooled to an initial temperature of 6o° F. at constant volume, what is its pressure for that condition? (c) Now if the air occupies such a volume as found in (a) and at an absolute pressure as determined in (b), at a temperature of 6o° F., and is then allowed to expand adiabatically down to atmospheric pressure (15 lbs.), what is the temperature and volume of the expanded air in Fahrenheit degrees? 8. Compare the work required to compress one pound of air from atmos- pheric pressure and a temperature of 6o° F. to a pressure of 200 lbs. per sq. in. absolute in (1) a one-stage and (2) in a two-stage compressor. Assume n = 1.25. 9. Using equation 249 as a basis, deduce a formula for the horse power required to abstract a given number of heat units per minute by an air refrigerating machine. 10. Calculate the approximate dimensions of a ten-ton air refrigerating machine and the power required to drive it. Pressure in the cold chamber is atmospheric and the temperature 32 F. Pressure of air delivered by compressor is 90 lbs. per sq. in. gage. The temperature of the air coming from condenser is 85 F. and the machine operates at 60 r.p.m. Allow 12 lbs. drop in pressure between the compressor and the expanding cylinder. 11. Calculate the approximate dimensions of a ten-ton ammonia com- pression refrigerating machine and the power required to drive it. The temperature in the expansion coils is 15 F. and the temperature in the con- denser is 8 5 F. The machine is double acting and operates at a speed of 80 r.p.m. 12. What is the ice-making capacity per twenty-four hours of the machine in problem 11? The temperature of the water to be frozen is 8o° F. APPENDIX Table I SPECIFIC HEAT OF GASES AND VAPORS (Taken from Smithsonian Physical Tables) Substance Air. Alcohol, (ethyl) Alcohol, (methyl) Ammonia . Benzene. Carbon Dioxide Carbon Monoxide Ether. Hydrogen. . Nitrogen Sulphur Dioxide Water Range of Temp.° C. -30-10 0-100 0-200 20-100 Mean 108-220 101-223 23-100 27-200 24-216 Mean 34-iiS 35-i8o 116-218 -28-77 15-100 11-214 Mean 23-99 26-198 69-224 27-189 25-1 1 1 Mean -28-9 12-198 21 — 100 Mean 0-200 16-202 128-217 100-125 Mean Cv 0.23771 0.23741 0.23751 0.2389 0.23788 0-4534 0.4580 0.5202 o.5356 0.5125 0.5228 0.2990 0.3325 0-3754 0.1843 0.2025 0.2169 0.2012 0.2425 0.2426 •4797 .4618 .4280 ■4565 •3996 .4090 .4100 .4062 .2438 ■1544 .4805 3787 4296 Authority Regnault 1 1 1 1 Wiedemann Regnault Regnault Wiedemann Regnault Wiedemann < < Regnault Regnault Wiedemann Regnault Wiedemann Regnault Wiedemann Regnault Regnault Regnault Gray, Macfarlane, Cv C V 1 .4066 i.i3 6 131 1.300 1-403 1 .029 1 .410 1 .410 1 .26 1.300 Authority Various Jaeger, j Neyreneuf / Cazin, Wiillner Wiillner Rontgen, Cazin, Wiillner Muller Cazin Cazin Cazin Muller Various Calcu- lated Co O.1691 O.3991 O.3991 O.1548 O.1729 O.4436 2.419 0.1729 O.1225 0.3305 197 198 APPENDIX Table II DENSITY OF GASES (Taken from Smithsonian Physical Tables) Gas Specific gravity Grams per cubic centimeter Pounds per cubic foot Air , Ammonia I .OOO 0.597 I.529 O.967 O.320-O.740 O.0696 1 .191 0.559 O.972 1 .105 2.247 O.OOI293 O.OOO770 O.OOI974 O.OO1234 . 000414-0 . 00095 7 0.000090 0.001476 0.000727 0.001257 0.001430 0.002785 O.08071 O.04807 O.12323 O.07704 O.02583-O.05973 0.00562 O.09214 0.04538 O.07847 O.08927 O.17386 Carbon dioxide. ...... Carbon monoxide Coal gas Hydrogen Hydrogen sulphide. . . Marsh gas Nitrogen Oxygen Sulphur dioxide APPENDIX 199 Density Weight per Cubic Foot, Pounds. 3 OO H OMOO PO W On rj- voO lOV)iO^- W)H O O von rrO n 10 w On O POO On cm 10OO m ^tf- N O N^tOvO hi O m\0 O "^O OOOhhihicmcmcmpo 1000 m POO 00 m POO 00 O OOOOOOOOOOOOHIMMHICMCMCMCMPO 000000000000000000000 000000000000000000000 a! p. •» PO Ovo NO 00 O O OOOOOOOOOnOvovoio pOOO 10 cm co co m po lO^H tj- CM HI N CM N PO POOO O PO HI fONNOO lO CM tO pi 't Q> ^ ^O HO f)N h OnNNiO'^-'^-pOpOpO Omo O no ioi- ^-t^toH w CM HI H Si + OO NIOO CM Tj- fO -r^.r^r^ CMCMCMCMCMCMCMHIHIHIHIHIHIHIH1HHHIHIHIH1 Entropy of the Vapor. k]I^ O r}- *0 O PO 10O NOO N h OO •^■■^•w O CM N 10O VO O POPOH lorCtNN CO Tj- M 00 M0000 O rr OO N.H n ^- h aNin^- ^too rj-Ooo 10 po cm 000 n w O O On On 000 00 00 00 r^O OO 10 10 10 10 10 "t ^|- CMCMCMHIHIHIHIHIHIHIHIHIH1HIHHIHIHIHHIH Entropy of the Liquid. <£> CM POO OO O^N !OlON O00 00 00 M O POO CM CM N O CM TJ- O CM CM HI OnO CM Tj- O Oi» Heat Equivalent of" Internal Work. a POM N ^VO On NOO N ©N'tO "3- O -^ CM -"tf- O00 00 N lO N CM NfOO N to CM O O 00 CM n cm 00 tt O n -^- M Q On OnOO O000 NNNio^J-rOrOM cm m m m O O O On On On On On On On On On On O On On On On On On On On M HI + II &5 NOO OnO O M POCM O^OO IOIONIOO M H ON to •sj- CM N M CM OnO f-~0 lOlOTj-T}--^POPOPOCM m O O On OnOO OOOO NN OOOOOOOOOOOOOOOnOnOnOnOnOOn HHMHHHMMHHMhHMM Heat of the Liquid. •« lOtOMOH TTOO tO H O CM to On N CO hi Tf POOO O 'ct - On h On NOO N h N a C)h N O N POOO HO On^OO O N -<3- O O h to On CM PO ^r ^" VO IOO O O "On O CM PO CO *3" 10 IOO MMMMMHMMHM Tempera- ture, Degrees F. - CO to On h 00 cmoOO co co to cm mOOO too N cm too O m tt OnO CO h 0 O "3-00 MO m pocm OO CMOO ro N H PO IOO N t>.00 On On On O CM tJ- 10O !>• r^OO 00 On On O Absolute Pressure, Pounds per Square Inch. ■fc. h cm po ^f IOO N00 On OOOOOOOOOmcmpOtJ- 10O N00 0> O h cm H — ■!■ ■!■ H M M a 200 APPENDIX < ft co. P ft H < ft ft O CO ft i— i ft ft ft O ft ft 3 < Density Weight per Cubic Foot, Pounds. § O 0\«\0 o POO toOW rrOO m ^ ifl io to »t (O N m O^t^'sJ-HOO PO to t^OO O^h N -t toO f^OO a O m N N POrj-iovo PO PO PO fO ^O t^OO OO H N W) toO t-»00 Os O m M OOOOOOOOOmi-iihmmmmmmw»0 Os to N O O **» PONNNNMHHM el + "t - N O w to M O O O O ■* » r-» N N r-» t>.vo OOOOOOOOOOOOOO MHMHMMHMHHtHHHMMMHHWI-tM Entropy of the Vapor. •^Ih Os po NO to ^t h O m •^-oo ON O TfO 00 to M M N N PO N >t h vO O hO rh rj-O O O PO Os NO O O O N so to tt tt OsO poOCOso -^pOih OOO NO to Tf PO N ^-^r^-TrPOCOCOCONNCSNNNMMHHHMH Entropy of the Liquid. <*> lO HI OO f)>0« OOO O M POO N TfM TJ- lO O ^" ^- PO N 00 h PO to PO00 so »tv.r^.t^t^t^r^t>»t>-t^t^.i>.r^ noo oo oo oo oo oo oo Heat Equivalent of Internal Work. a O <0O 000000 O w Os CO O NO rt-PO tOOO PO O NO »r^ l>-00 OO 00 00 00 00 WMHHHWHMMMHHMHMHIIHI-IHIMH HHHMHWMHH.HMMHHMMMHMMH Heat of Vaporiza- tion. hj M ON'Jtt^O O m OsPONtoO O^O N N(Oh OsOsO Tf H O Os O -0 POOO -00 OOOsOMNPO^to too O t*» t>-O0 OO Os Os Os HMHHMNNNNNNNNCNNNCSNNNCS Tempera- ture, Degrees F. - MOO OOtoO O O m POPOPOtoO h t^ O OsO ^0 pO O 00 lO Os N POOO O O ON't H N N00 N t>-NO O ^ t"* O O h h n ^io toO t^oo OOOsOsOOmmnnn NNNNNNNlNN^- i^O t^OO O O m cn co ■>*• 100 t^OO O cn ■<*■ O tj- - to ■<*■ m On cn cn O rf- co to cn CO00 O O O t^. r^OO H \0 TJ- rj- O O M com m m CN toiONO COO O Tt" On COOO co On tJ- O CN tOOO to co cn m O QnCO r-^O Oio^-^-cocncnmihOOO OnOO O to Tf ^ tO to to to COCOCOCOCNCN*CNCNCNCNCNCNCNCNCNCNCNCNCNCNMMMM O cn r^ co On r-* 00 ^O Nt^O O O OnOO 00 00 to to to to to to r^f^O\■ f>-00 0O O Os ON O O M M M CM » t^OO O HI COO m CN cm CN cn cn cn cocOfOfOCOCTO(Oit , ti - i'i' , t't , t , J -, t^' l/ ' l O , O l O 0OOOOOOO0O0OO00OO0COO0OOO00OOO00O00OO0O00O0OO0O0O0O0OO000O0O »0 N aMO O toO N^-HOOO iO'^-'!i- , ^-^-^J- too 00 O CO tOOO "cj- CN 00 COO N lO N O MO N 000 to CO M O^N") fO H O^t^lO-^-CN O 00 tO- f*~ r^NO OOOO totototototo-rtTj-TfcoCN cn 0000 cOOO cn 00 'd-O toO rj- On rt-oO f^NH tooo cm O On cn On tooo h t^00 00 On O m 00 00 OO 00 On On m cn cn co^Tl-toto too O r*» t^-00 0000 O^ ON On O O m cn^ OnO^OnOnO^OnOnOnOnOnO^OnOnOnCnOnO^O^O^O o o o o CN tOOO N Nt-00 OO O O cn tJ-O On cn •rj-oo io ^OO co to cn ONt^^J"ONH lOTfCN CN CN CN cOcO0 O m cococococococococococococococococooO O O toO CO Tf ^ to toO O f^ t~^O0 OOOiO>OOhhN(NI«5tj->ONO 202 APPENDIX Table IV. — PROPERTIES OF SUPERHEATED STEAM Reproduced by permission from Marks and Davis' "Steam Tables and Diagrams." (Copyright, 1909, by Longmans, Green & Co.) Pressure, Satu- Degrees of Superheat. Pressure, Pounds rated Pounds Absolute. Steam. 50 100 150 200 250 300 Absolute. t 162.3 212.3 262 .3 312.3 362.3 412.3 462.3 / 5 V 73-3 79-7 85-7 91.8 97-8 103.8 109.8 V 5 h "30- 5 H53-5 1176.4 H99-5 1222 .5 1245.6 1268.7 h t 193.2 243.2 293.2 343-2 393-2 443-2 493-2 t 10 V 38.4 4i-5 44.6 47-7 50.7 53-7 56.7 V 10 h 1143.1 1166.3 1189.5 1212 .7 1236.0 1259-3 1282.5 h t 213.0 263 .0 3I3-0 363-0 4i3-o 463.0 5i3- t *5 V 26.27 28.40 30.46 32.50 34-53 36.56 38.58 V 15 h 1150.7 1174.2 1197.6 1221 .0 1244.4 1267 .7 1291 .1 h t 228.0 278.0 328.O 378.0 428.0 478.0 528.0 t 20 V 20.08 21 .69 23-25 24.80 26.33 27-85 29-37 V 20 h 1156.2 1179.9 1203.5 1227. 1 1250.6 1274-1 1297.6 h t 240.1 290.1 340.I 390.I 440.1 490.1 54o.i t 25 V 16.30 17 .60 18.86 20.10 21.32 22.55 23-77 V 25 h 1160.4 1 184. 4 1208.2 1231-9 1255-6 1279.2 1302 .8 h t 250.4 300.4 350.4 400.4 45o.4 500.4 55o.4 t 30 V 13-74 14-83 15.89 16.93 17.97 18.99 20.00 V 30 h 1163.9 1188.1 1212 .1 1236 .0 12597 1283.4 1307-1 h t 259-3 309-3 359-3 409-3 459-3 509-3 559-3 t 35 V 11.89 12.85 13-75 14.65 15-54 16.42 17.30 V 35 h 1166.8 1191.3 1215-4 1239.4 1263.3 1287. 1 1310.8 h t 267.3 317-3 367.2 417-3 467-3 517-3 567-3 t 40 V 10.49 n-33 12.13 12.93 13.70 14.48 15-25 V 40 h 1169.4 1 194.0 1218.4 1242 .4 1266.4 1290.3 1314.1 h t 274-5 324-5 374-5 424-5 474-5 524-5 574-5 t 45 V 9-39 10.14 10.86 n-57 12 .27 12 .96 1365 V 45 h 1171 .6 1196.6 1221 .0 1245.2 1269.3 1293.2 1317.0 h t 281 .0 33IO 381.0 431.0 481 .0 53i -o 581.0 t 50 V 8.51 9.19 9.84 10.48 11 .11 11.74 12.36 V 5o h 1173.6 1198.8 1223.4 1247.7 1271 .8 1295.8 I3I9-7. h t 287.1 337-1 387-1 437-1 487.1 537-1 587.1 t 55 V 7.78 8.40 9.00 9-59 10.16 10.73 11.30 V 55 h H75-4 1 200 . 8 1225.6 1250.0 1274.2 1298. 1 1322.0 h t 292 .7 342.7 392.7 442.7 492.7 542.7 592.7 t 60 V 7.17 7-75 8.30 8.84 9-36 9.89 10.41- V 60 h 1177.0 1202 .6 1227.6 1252. 1 1276.4 1300.4 1324-3 h t 298.0 348.0 398 -o 448.0 498.0 548.0 598.0 t 65 V 6.65 7.20 7.70 8.20 8.69 9.17 9-65 V 65 h 1178.5 1204.4 1229.5 1254.0 . 1278.4 1302.4 1326.4 h t 302.9 352.9 402.9 452.9 502.9 552.9 602.9 t 70 v. 6.20 6.71 7.18 7-65 8. 11 8.56 9.01 V 70 h 1179.8 1205.9 1231 .2 1255-8 1280.2 1304-3 1328.3 h t 307.6 357-6 407.6 457-6 507.6 557-6 607.6 t 75 V 5.8i 6.28 6.73 7.17 7.60 8.02 8.44 V 75 h 1181.1 1207.5 1232 .8 1257-5 1282 .0 1306. 1 1330 - 1 h t 312.0 362 .0 412 .0 462 .0 512.0 562.0 612 .0 t 80 V 5-47 5-92 6-34 6-75 7.17 7.56 7-95 V 80 h 1182.3 1208.8 1234.3 1259.0 1283.6 1307.8 I33L9 h t 3i6-3 366.3 416.3 466.3 516.3 566.3 616.3 t 85 V 5-i6 5-59 6-99 6.38 6.76 7.14 7-51 V 85 h 1183.4 1210. 2 1235-8 1260.6 1285.2 I309-4 1333-5 h t = Temperature, deg. Fahr. v = Specific volume, in cubic feet, per pou tid. h = Tot£ d heat froi n water at 32 degree s, B.t.u. APPENDIX Table IV. — Continued 203 Pressure, Satu- Degrees of Superheat. Pressure, Pounds Absolute. rated Steam. Pounds Absolute. 50 IOO 150 200 250 300 t 320.3 370.3 420.3 470.3 520.3 570.3 620.3 t 90 V 4.89 5-29 5-67 6.04 6.40 6.76 7 11 V 90 h 1184.4 I2II .4 1237.2 1262 .0 1286.6 1310.8 1334 9 h t 324-1 374-1 424.1 474-1 524-1 574-1 624 1 t 95 V 4-65 5-03 5-39 5-74 6.09 6-43 6 76 V 95 h 1185.4 1212 .6 1238.4 1263.4 1288. 1 1312.3 1336 4 h t 327.8 377-8 427.8 477-8 527.8 577-8 627 8 t IOO V 4-43 4-79 5-i4 5-47 5.80 6.12 6 44 V IOO h 1186.3 1213.8 1239.7 1264.7 1289.4 1313-6 1337 8 h t 331-4 381.4 431-4 481.4 531-4 581.4 631 4 t 105 V 4-23 4-58 4.91 5-23 5-54 5-8 5 6 15 V 105 h 1187.2 1214.9 1 240 . 8 1265.9 1290.6 13*4-9 1339 1 h t 334-8 384-8 434-8 484.8 534-8 584.8 634 8 t no V 4-05 4-38 4.70 5-oi 5-3i 5-6i 5 90 V no h 1188.0 1215.9 1242 .0 1267. 1 1291 .9 1316.2 1340 4 h t 338.1 388.1 438.1 488.1 538.1 588.1 638 1 t 115 V 3-88 4.20 4-5i 4.81 5-09 5-38 5 66 V II 5 h 1188.8 1216.9 1243. 1 1268.2 1293.0 I3I7-3 1341 5 h t 341-3 391-3 441-3 491-3 541-3 591-3 641 3 t 120 V 3-73 4.04 4-33 4.62 4.89 5-i7 5 44 V 120 h 1189.6 1217.9 1244. 1 1269.3 1 294. 1 1318.4 1342 7 h t ' 344-4 394-4 444.4 494.4 544-4 594-4 644 4 t 125 V 3-58 3.88 4-i7 4-45 4-7i 4-97 5 23 V I2 5 h 1190.3 1218.8 1245. 1 1270.4 1295.2 I3I9-5 1343 8 h t 347-4 397-4 447-4 497-4 547-4 597-4 647 4 t 130 V 3-45 3-74 4.02 4.28 4-54 4.80 5 05 V 130 h 1191 .0 1219.7 1246. 1 1271 .4 1296.2 1320.6 1344 9 h t 35o.3 400.3 45o.3 500.3 55o.3 600.3 650 3 t 135 V 3-33 3.61 3.88 4.14 4.38 4-63 4 87 V J 35 h 1191 .6 1220.6 1247.0 1272.3 1297 .2 1321 .6 1345 9 h t 353 - 1 403- 1 453-1 503- 1 553-1 603.1 653 1 t 140 V 3-22 3-49 3-75 4.00 4.24 4.48 4 7i V 140 h 1192 .2 1221 .4 1248.0 1273-3 1298.2 1322 .6 1346 9 h t 355-8 405.8 455-8 505-8 555-8 605.8 655 8 t 145 V 3.12 3-38 3 63 3-87 4.10 4-33 4 56 V J 45 h 1192 .8 1222 .2 1248.8 1274.2 1 299. 1 1323.6 1347 9 h t 358.5 408.5 458.5 508.5 558.5" 608.5 658 5 t 150 V 3.01 3-27 3-5i 3-75 3-97 4.19 4 41 V 150 h H93-4 1223 .0 1249.6 1275. 1 1300.0 1324-5 1348 8 h t 361.0 411 .0 461 .0 511. 561.0 611 .0 661 t 155 V 2 .92 3-*7 3-4i 3-t>3 3-85 4.06 4 28 V !55 h 1 194.0 1223 .6 1250.5 1276.0 1300.8 13253 1349 7 h t 363-6 413.6 463-6 513-6 563-6 613.6 663 6 t 160 V 2.83 3-07 3-3o 3-53 3-74 3-95 4 15 V 160 h "94-5 1224.5 1251.3 1276.8 1301.7 1326 . 2 1350 6 h t 366.0 416.0 466.0 516.0 566.0 616.0 666 t 165 V 2-75 2.99 3.21 3-43 3 64 3 84 4 04 V 165 h 1195.0 1225 . 2 1252.0 1277.6 1302.5 1327-1 i35i 5 h t 368.5 418.5 468.5 518.5 568.5 618.5 668 5 t 170 V 2.68 2 .91 3.12 3-34 3-54 3-73 3 92 V 170 h II95-4 1225.9 1252.8 1278.4 I303-3 1327.9 1352.3 h t — Temperature, deg. Fahr. v = Specific volume, in cubic feet, per pound. h = Total heat from water at 32 degrees, B.t.u. 204 APPENDIX Table IV. — Continued Pressure, Satu- Degrees of Superheat. Pressure. Pounds T~% Absolute. IdLLU Steam. irounas Absolute So 100 150 200 250 300 t 370.8 420.8 470.8 520.8 57o.8 620.8 670.8 t 175 V 2 .60 2.83 3 04 3-24 3-44 3 63 3-82 V 175 h H95-9 1226.6 1253.6 1279. 1 1304-1 1328.7 1353-2 h t 373-1 423.1 473-1 523-1 573-1 623.1 673.1 t 180 V 2-53 2-75 2 .96 3.16 3-35 3-54 3-72 V 180 h 1196.4 1227. 2 1254-3 1279.9 1304.8 13295 1353-9 h t 375-4 425-4 475-4 525-4 575-4 625.4 675-4 t 185 V 2.47 2.68 2.89 3.08 3-27 3-45 3 63 V 185 h 1196.8 1227.9 1255-0 1280.6 1305-6 1330.2 1354-7 h t 377-6 427.6 477.6 527.6 577-6 627.6 677.6 t 190 V 2 .41 2 .62 2.81 3.00 3-19 3-37 3-55 V 190 h H97-3 1228.6 1255-7 1281.3 1306.3 1330.9 1355-5 h t 379-8 429.8 479.8 529.8 579-8 629.8 679.8 t 195 V 2-35 2-55 -2.75 2-93 3-ii 3-29 3 46 V i95 h 1197.7 1229.2 1256.4 1282 .0 1307.0 1331-6 1356.2 h t 381.9 431-9 481.9 531-9 581.9 631.9 681.9 t 200 V 2 .29 2.49 2.68 2.86 3-04 3.21 3-38 V 200 h 1198.1 1229.8 1257. 1 1282 .6 1307.7 1332.4 1357 h t 384.0 434 -o 484.0 534 584.0 634.0 684.0 t 205 V 2.24 2-44 2 .62 2.80 2.97 3 14 3 30 V 205 h 1198.5 1230.4 1257-7 1283.3 1308.3 i333-o 1357-7 h t 386.0 436.0 486.0 536.o 586.0 636.0 686.0 t 210 V 2 .19 2.38 2.56 2.74 2 .91 3-07 3-23 V 210 h 1198.8 1 231 .0 1258.4 1284.0 1309.0 1333-7 1358.4 h t 388.0 438.0 488.0 538.o 588.0 638.0 688.0 t 215 V 2 .14 2-33 2.51 2.68 2.84 3.00 3.16 V 215 h 1199.2 1231 .6 1259.0 1284.6 1309 . 7 1334-4 1359- 1 h t 389-9 439-9 489.9 539-9 589-9 639-9 689.9 t 220 V 2 .09 2.28 2-45 2 .62 2.78 2-94 3.10 V 220 h 1199.6 1232 .2 1259.6 1285 .2 i3 IO -3 1335- 1 1359-8 h t 39 J -9 441.9 491.9 541-9 591-9 641.9 691.9 t 225 V 2.05 2.23 2 .40 2-57 2 .72 2.88 3-03 V 225 h 1199.9 1232.7 1260.2 1285.9 1310.9 1335-7 1360.3 h t 393-8 443-8 493-8 543-8 593-8 643-8 693-8 t 230 V 2 .00 2.18 2-35 . 2.51 2 .67 2.82 2.97 V 230 h 1200.2 1233.2 1260.7 1286.5 1311.6 1336.3 1361 .0 h t 395-6 445-6 495-6 545-6 595-6 645.6 695.6 t 235 V 1 .96 2 .14 2.30 2.46 2 .62 2-77 2 .91 V 235 h 1 200 . 6 1233-8 1261 .4 1287. 1 1312 . 2 I337-0 1361.7 h t 397-4 447-4 497-4 547-4 597-4 647.4 697.4 t 240 V 1 .92 2 .09 2 .26 2 .42 2-57 2 .71 2.85 V 240 h 1200.9 1234-3 1261 .9 1287.6 1312.8 1337-6 1362.3 h t 399-3 449-3 499-3 549-3 599-3 649-3 699-3 t 245 V 1.89 2.05 2 .22 2-37 2.52 2.66 2.80 V 245 h 1 201 .2 1234.8 1262 .5 1288.2 I3I3-3 1338.2 1362.9 h t 401 .0 451.0 501.0 55i -o 601 .0 651.0 701 .0 t 250 V 1-85 2 .02 2 .17 2-33 2-47 2 .61 2-75 V 250 h 1201.5 1235-4 1263 .0 1288.8 13*3-9 1338.8 1363-5 h t 402 .8 452.8 502.8 552.8 602.8 652.8 702.8 t 255 V 1. 81 1.98 2 .14 2.28 2-43 2.56 2 .70 V 255 h 1 201 .8 12359 1263 .6 1289.3 1314-5 1339-3 1364-1 h t = Temperature, deg. Fahr. v = Specific volume, in cubic feet, per pound. h = Total heat from water at 32 degrees, B.t.u. APPENDIX 205 Table V. — SATURATED VAPOR OF SULPHUR DIOXIDE Reproduced by permission from Peabody's " Steam and Entropy Tables." English Units. fii uA g -4-> G 0>«-i a Temperatui Degrees Fa renheit. Pressure, Pounds pe Square Inc •G . "o'g -n cr ■ U l-H O HH ft > Heat Equiva of Interna Work. Heat Equival of Externa Work. P. o* c !3 > '0 a> Pi t P A H L P Apu 9 5 -40 3-14 -29 166 195 182 13 —0.0632 23.O — -20 5 90 — 21 169 190 176 14 -0.0447 12.7 O io.35 -13 172 185 170 15 —0.0268 7-54 IO i3-4i - 9 173 182 167 15 —0.0182 5-93 20 I7-I5 - 5 174 179 164 15 —0.0098 4.72 30 21 .66 — I 176 177 162 15 —0.0016 3.8i 40 27.06 3 177 174 158 16 . 0064 3.10 50 33-45 7 178 171 155 16 0.0144 2.58 60 40.98 11 179 168 152 16 0.0221 2. 11 70 49-75 15 181 166 ISO 16 0.0297 1.78 Table VI. — PROPERTIES OF CARBON DIOXIDE Reproduced from Marks' " Mechanical Engineers' Handbook." .fe-8 Heat Content G UO G u O G 13 13 S 3 "o -nperatu grecs F, renheit J3 coi-i 13 n ; Equiv Extern Work *o > §•3 w G £; G-— 3 ° (D Pi m ►h O 03 t £ h ' H z. P .A^M s 20 221 .O -24-75 IOO.50 125-25 IO9.O 16.3 0.4173 -O.0513 308.O — 16.00 101 .00 117 00 IOI 3 15-7 0.2918 -O.0325 10 362.5 -11.36 100.89 112 35 96 9 15-4 0.2450 — O.0227 20 421 .6 — 6.40 100.43 I06 83 91 8 150 . 2060 — O.OI26 30 488.8 — 1 .04 99-43 IOO 47 86 7 14.2 0.1724 — 0.002I 40 564-5 4-36 98.25 93 89 80 4 13-5 0.1444 O.O087 50 650.0 10.76 96.30 85 54 73 3i 12.2 0.1205 O.O205 60 744.o 17-85 93-54 75 69 64 90 10.8 0.0986 O.0334 70 847.0 26.02 89-35 63 33 54 03 9-3 0.0816 O.0483 Table VII. — NAPERIAN LOGARITHMS Reproduced by permission from Goodenough's " Properties of Steam and Ammonia." e =2.7182818 log e = 0.4342945 = M 1.0 1.1 1.2 1.3 1.4 1.5 1.6 1.7 1.8 1.9 2.0 2.1 2.2 2.3 2.4 2.5 2.6 2.7 2.8 2.9 3.0 3.1 3.2 3.3 3.4 3.5 3.6 3.7 3.8 3.9 4.0 4.1 4.2 4.3 4.4 4.5 4.6 4.7 4.8 4.9 5.0 5.1 5.2 5.3 5.4 5.5 5.6 0. 0000 0.09531 0.1823 0.2624 0.3365 0. 4055 0. 4700 0.5306 0.5878 0.6418 0.6931 0.7419 0.7884 0.8329 0.8755 0.9163 0.9555 0.9933 1.0296 1.0647 1.0986 1.1314 1.1632 1.1939 1.2238 1.2528 1.2809 1.3083 1.3350 1.3610 1.3863 1.4110 1.4351 1.4586 1.4816 1.5041 1.5261 1.5476 1.5686 1.5892 1.6094 1.6292 1.6487 1.6677 1.6864 1.7047 1.7228 1.6114 1.6312 1.6506 1.6696 1.6882 1.7066 1.7246 0.00995 0. 1044 0. 1906 0. 2700 0.3436 0.4121 0.4762 0.5365 0.5933 0.6471 0.6981 0.7467 0.7930 0.8372 0.8796 0.9203 0.9594 0.9969 1.0332 0682 1.1019 1.1346 1.1663 1.1969 1.2267 1.2556 1.2837 1.3110 1.3376 1.3635 1.3888 1.4134 1.4375 1.4609 1.4839 1.5063 1.5282 1.5497 1.5707 1.5913 0.01980 0.1133 0. 1988 0.2776 0.3507 0.4187 0. 4824 0.5423 0.5988 0.6523 0.7031 0.7514 0.7975 0.8416 0.8838 0.9243 0.9632 1.0006 1.0367 1.0716 1.1053 1.1378 1.1410 1.1694 1.1725 1.2000 1.2030 0.02956 0.1222 0.2070 0. 2852 0.3577 0.4253 0. 4886 0.5481 0. 6043 0.6575 0. 7080 0.7561 0.8020 0.8459 0.8879 0.9282 0.9670 1.0043 1.0403 1.0750 1.1086 1.1119 0.03922 0.1310 0.2151 0.2927 0.3646 0.4318 0.4947 0.5539 0.6098 0.6627 0.7129 0.7608 0.8065 0. 8502 0. 8920 0.9322 0.9708 1.0080 1.0438 1.0784 1.2296 1.2585 1.2865 1.3137 1.3403 1.3661 1.3913 1.4159 1.4398 1.4633 1.4861 1.5085 1.5304 1.5518 1.5728 1.5933 1.6134 1.6332 1.6525 1.6715 1.6901 1.7884 1.7263 1.2326 1.2613 1.2892 1.3164 1.3429 1.3686 1.3938 1.4183 1.4422 1.4656 1.4884 1.5107 1.5326 1.5539 1.5748 1.5953 1.6154 1.6351 1.6544 1.6734 1.6919 1.7102 1.7281 1.1442 1.1756 1.2060 1.2355 1.2641 1.2920 1.3191 1.3455 1.3712 1.3962 1.4207 1.4446 1.4679 1.4907 1.5129 1.5347 1.5560 1.5769 1.5974 1.6174 1.6371 1.6563 1.6752 1.6938 1.7120 1.7299 206 0. 04879 0. 1398 0.2231 0.3001 0.3716 0.4382 0.5008 0.5596 0.6152 0. 6678 0.7178 0.7655 0.8109 0. 8544 0.8961 0.9361 0.9746 1.0116 1.0473 1.0818 1.1151 1.1474 1.1787 1.2090 1.2384 1.2669 1.2947 1.3218 1.3481 3737 1.3987 1.4231 1.4469 1.4702 1.4929 1.5151 1.5369 1.5581 1.5790 1.5994 1.6194 1.6390 1.6582 1.6771 1.6956 1.7138 1.7317 0.05827 0. 1484 0.2311 0.3075 0.3784 0.4447 0.5068 0. 5653 0. 6206 0.6729 0. 7227 0.7701 0.8154 0. 8587 0.9002 0.9400 0.9783 1.0152 1.0508 1.0852 1.1184 1.1506 1.1817 1.2119 1.2413 1.2698 1.2975 1.3244 1.3507 1.3762 0. 06766 0. 1570 0.2390 0.3148 0.3853 0.4511 0.5128 0.5710 0.6259 0. 6780 0.7275 0. 7747 0.8198 0.8629 0.9042 0.9439 0.9821 1.0188 1.0543 1.0886 1.1217 1.1537 1.1848 1.2149 1.2442 1.2726 1.3002 1.3271 1.3533 1.3788 8 1.4012 1.4036 1.4061 1.4255 1.4493 1.4725 1.4951 1.5173 1.5390 1.5602 1.5810 1.6014 1.6214 1.6409 1.6601 1.6790 1.6974 1.7156 1.7334 0. 07696 0. 1655 0.2469 0. 3221 0.3920 0.4574 0.5188 0. 5766 0.6313 0.6831 0.7324 0.7793 0.8242 0.8671 0.9083 0. 9478 0. 9858 0.08618 0. 1739 0.2546 0.3293 0.3988 0.4637 0.5247 0. 5822 0.6366 0.6881 0.7372 0. 7839 0.8286 0.8713 0.9123 0.9517 0.9895 1.0225 1.0260 1.0578 1.0613 1.0919 1.0953 1.1249 1.1282 1.1569 1.1878 1.2179 1.2470 1.2754 1.3029 1.3297 1.3558 1.3813 1.4279 1.4516 1.4748 1.4974 1.5195 1.5412 1.5623 1.5831 1.6034 1.6233 1.6429 1.6620 1.6808 1.6993 1.7174 1.7352 1.4303 1.4540 1.4770 1.4996 1.5217 1.5433 1.5644 1.5851 1.6054 1.6253 1.6448 1.6639 1.6827 1.7011 1.7192 1.7370 1.1600 1.1909 1.2208 1.2499 1.2782 1.3056 1.3324 1.3584 1.3838 1.4085 1.4327 1.4563 1.4793 1.5019 1.5239 1.5454 1.5665 1.5872 1.6074 1.6273 1.6467 1.6658 1.6845 1.7029 1.7210 1.7387 Table VII. — Continued. NAPERIAN LOGARITHMS 1 2 3 4 5 6 7 8 9 5.7 5.8 5.9 1.7405 1.7579 1.7750 1.7422 1.7596 1.7766 1.7440 1.7613 1.7783 1.7457 1.7630 1.7800 1.7475 1.7647 1.7817 1.7492 1.7664 1.7834 1.7509 1.7681 1.7851 1.7527 1.7699 1.7867 1.7544 1.7716 1.7884 1.7561 1.7733 1.7901 6.0 1.7918 1.7934 1.7951 1.7967 1.7984 1.8001 1.8017 1.8034 1.8050 1.8066 6.1 6.2 6.3 1.8083 1.8245 1.8405 1.8099 1.8262 1.8421 1.8116 1.8278 1.8437 1.8132 1.8294 1.8453 1.8148 1.8310 1.8469 1.8165 1.8326 1.8485 1.8181 1.8342 1.8500 1.8197 1.8358 1.8516 1.8213 1.8374 1.8532 1.8229 1.8390 1.8547 6.4 6.5 6.6 1.8563 1.8718 1.8871 1.8579 1.8733 1.8886 1.8594 1.8749 1.8901 1.8610 1.8764 1.8916 1.8625 1.8779 1.8931 1.8641 1.8795- 1.8946 1.8656 1.8810 1.8961 1.8672 1.8825 1.8976 1.8687 1.8840 1.8991 1.8703 1.8856 1.9006 6.7 6.8 6.9 1.9021 1.9169 1.9315 1.9036 1.9184 1.9330 1.9051 1.9199 1.9344 1.9066 1.9213 1.9359 1.9081 1.9228 1.9373 1.9095 1.9242 1.9387 1.9110 1.9257 1.9402 1.9125 1.9272 1.9416 1.9140 1.9286 1.9430 1.9155 1.9301 1.9445 7.0 1.9459 1.9473 1.9488 1.9502 1.9516 1.9530 1.9544 1.9559 1.9573 1.9587 7.1 7.2 7.3 L9601 1.9741 1.9879 1.9615 1.9755 1.9892 1.9629 1.9769 1.9906 1.9643 1.9782 1.9920 1.9657 1.9796 1.9933 1.9671 1.9810 1.9947 1.9685 1.9824 1.9961 1.9699 1.9838 1.9974 1.9713 1.9851 1.9988 1.9727 1.9865 2.0001 7.4 7.5 7.6 2.0015 2.0149 2.0281 2.0028 2.0162 2.0295 2. 0042 2.0176 2.0308 2.0055 2.0189 2.0321 2.0069 2.0202 2. 0334 2. 0082 2.0215 2. 0347 2.0096 2.0229 2.0360 2.0109 2.0242 2.0373 2.0122 2.0255 2.0386 2.0136 2.0268 2.0399 7.7 7.8 7.9 2.0412 2.0541 2.0668 2. 0425 2.0554 2.0681 2.0438 2.0567 2.0694 2.0451 2.0580 2.0707 2. 0464 2.0592 2.0719 2. 0477 2.0605 2.0732 2. 0490 2.0618 2.0744 2.0503 2.0631 2.0757 2.0516 2.0643 2.0769 2.0528 2.0656 2. 0782 8.0 2.0794 2.0807 2.0819 2.0832 2.0844 2.0857 2.0869 2.0881 2.0894 2.0906 8.1 8.2 8.3 2.0919 2.1041 2-1163 2.0931 2.1054 2.1175 2.0943 2.1066 2.1187 2.0956 2.1078 2.1199 2.0968 2.1090 2.1211 2. 0980 2.1102 2. 1223 2.0992 2.1114 2.1235 2. 1005 2.1126 2. 1247 2.1017 2.1138 2.1258 2. 1029 2.1150 2. 1270 8.4 8.5 8.6 2. 1282 2.1401 2.1518 2. 1294 2.1412 2.1529 2.1306 2.1424 2. 1541 2.1318 2.1436 2.1552 2.1330 2. 1448 2.1564 2.1342 2.1459 2.1576 2.1353 2.1471 2.1587 2.1365 2. 1483 2. 1599 2. 1377 2.1494 2.1610 2.1389 2.1506 2. 1622 8.7 8.8 8.9 2.1633 2. 1748 2.1861 2. 1645 2.1759 2.1872 2.1656 2. 1770 2. 1883 2.1668 2.1782 2. 1894 2.1679 2.1793 2. 1905 2.1691 2.1804 2.1917 2. 1702 2.1815 2. 1928 2.1713 2.1827 2.1939 2.1725 2.1838 2.1950 2.1736 2.1849 2.1961 9.0 2.1972 2.1983 2.1994 2.2006 2.2017 2.2028 2.2039 2.2050 2.2061 2.2072 9.1 9.2 9.3 2.2083 2.2192 2.2300 2.2094 2.2203 2.2311 2.2105 2.2214 2.2322 2.2116 2.2225 2.2332 2.2127 2.2235 2.2343 2.2138 2. 2246 2.2354 2.2148 2.2257 2.2364 2.2159 2.2268 2.2375 2.2170 2.2279 2.2386 2.2181 2.2289 2.2396 9.4 9.5 9.6 2. 2407 2.2513 2.2618 2.2418 2.2523 2.2628 2. 2428 2.2534 2.2638 2. 2439 2.2544 2.2649 2. 2450 2. 2555 2.2659 2.2460 2.2565 2. 2670 2.2471 2.2576 2.2680 2.2481 2.2586 2.2690 2.2492 2.2597 2.2701 2. 2502 2.2607 2.2711 9.7 9.8 9.9 2.2721 2.2824 2. 2925 2.2732 2.2834 2.2935 2.2742 2. 2844 2.2946 2.2752 2.2854 2.2956 2.2762 2.2865 2.2966 2.2773 2.2875 2.2976 2.2783 2. 2885 2.2986 2.2793 2.2895 2.2996 2.2803 2.2905 2.3006 2.2814 2.2915 2.3016 10.0 2.3026 207 Table VIII. — LOGARITHMS Reproduced by permission from Goodenough's " Properties of Steam and Ammonia." Nat. Nos. Proportional Parts. 1 2 3 4 5 6 7 8 9 1 2 3 4 5 6 7 8 9 10 0000 0043 0086 0128 0170 0212 0253 0294 0334 0374 4 8 12 17 21 25 29 33 37 11 0414 0453 0492 0531 0569 0607 0645 0682 0719 0755 4 8 11 15 19 23 26 30 34 12 0792 0828 0864 0899 0934 0969 1004 1038 1072 1106 3 7 10 14 17 21 24 28 31 13 1139 1173 1206 1239 1271 1303 1335 1367 1399 1430 3 6 10 13 16 19 23 26 29 14 1461 1492 1523 1553 1584 1614 1644 1673 1703 1732 3 6 9 12 15 18 21 24 27 15 1761 1790 1818 1847 1875 1903 1931 1959 1987 2014 3 6 8 11 14 17 20 22 25 16 2041 2068 2095 2122 2148 2175 2201 2227 2253 2279 3 5 8 11 13 16 18 21 24 17 2304 2330 2355 2380 2405 2430 2455 2480 2504 2529 2 5 7 10 12 15 17 20 22 18 2553 2577 2601 %25 2648 2672 2695 2718 2742 2765 2 5 7 9 12 14 16 19 21 19 2788 2810 2833 2856 2878 2900 2923 2945 2967 2989 2 4 7 9 11 13 16 18 20 20 3010 3032 3054 3075 3096 3118 3139 3160 3181 3201 2 4 6 8 11 13 15 17 19 21 3222 3243 3263 3284 3304 3324 3345 3365 3385 3404 2 4 6 8 10 12 14 16 18 22 ' 3424 3444 3464 3483 3502 3522 3541 3560 3579 3598 2 4 6 8 10 12 14 15 17 23 3617 3636 3655 3674 3692 3711 3729 3747 3766 3784 2 4 6 7 9 11 13 15 17 24 3802 3820 3838 3856 3874 3892 3909 3927 3945 3962 2 4 5 7 9 11 12 14 16 25 3979 3997 4014 4031 4048 4065 4082 4099 4116 4133 2 3 5 7 9 10 12 14 15 26 4150 4166 4183 4200 4216 4232 4249 4265 4281 4298 2 3 5 7 8 10 11 13 15 27 4314 4330 4346 4362 4378 4393 4409 4425 4440 4456 2 3 5 6 8 9 11 13 14 28 4472 4487 4502 4518 4533 4548 4564 4579 4594 4609 2 3 5 6 8 9 11 12 14 29 4624 4639 4654 4669 4683 4698 4713 4728 4742 4757 1 3 4 6 7 9 10 12 13 30 4771 4786 4800 4814 4829 4843 4857 4871 4886 4900 1 3 4 6 7 9 10 11 13 31 4914 4928 4942 4955 4969 4983 4997 5011 5024 5038 1 3 4 6 7 8 10 11 12 32 5051 5065 5079 5092 5105 5119 5132 5145 5159 5172 1 3 4 5 7 8 9 11 12 33 5185 5198 5211 5224 5237 5250 5263 5276 5289 5302 1 3 4 5 6 8 9 10 12 34 5315 5328 5340 5353 5366 5378 5391 5403 5416 5428 1 3 4 5 6 8 9 10 11 35 5441 5453 5465 5478 5490 5502 5514 5527 5539 5551 1 2 4 5 6 7 9 10 11 36 5563 5575 5587 5599 56115623 5635 5647 5658 5670 1 2 4 5 6 7 8 10 11 37 5682 5694 5705 5717 5729 5740 5752 5763 5775 5786 1 2 3 5 6 7 8 9 10 38 5798 5809 5821 5832 5843 5855 5866 5877 5888 5899 12 3 5 6 7 8 9 10 39 5911 5922 5933 5944 5955 5966 5977 5988 5999 6010 1 2 3 4 5 7 8 9 10 40 6021 6031 6042 6053 6064 6075 6085 6096 6107 6117 1 2 3 4 5 6 8 9 10 41 6128 6138 6149 6160 6170 6180 6191 6201 6212 6222 1 2 3 4 5 6 7 8 9 42 6232 6243 6253 6263 6274 6284 6294 6304 6314 6325 1 2 3 4 5 6 7 8 9 43 6335 6345 6355 6365 6375 6385 6395 6405 6415 6425 1 2 3 4 5 6 7 8 9 44 6435 6444 6454 6464 6474 6484 6493 6503 6513 6522 1 2 3 4 5 6 7 8 9 45 6532 6542 6551 6561 6571 6580 6590 6599 6609 6618 1 2 3 4 5 6 7 8 9 46 6628 6637 6646 6656 6665 6675 6684 6693 6702 6712 1 2 3 4 5 6 7 7 8 47 6721 6730 6739 6749 6758 6767 6776 6785 6794 6803 1 2 3 4 5 5 6 7 8 48 6812 6821 6830 6839 6848 6857 6866 6875 6884 6893 1 2 3 4 4 5 6 7 8 49 6902 6911 6920 6928 6937 6946 6955 6964 6972 6981 1 2 3 4 4 5 6 7 8 50 6990 6998 7007 7016 7024 7033 7042 7050 7059 7067 1 2 3 3 4 5 6 7 8 51 7076 7084 7093 7101 7110 7118 7126 7135 7143 7152 1 2 3 3 4 5 6 7 8 52 7160 7168 7177 7185 7193 7202 7210 7218 7226 7235 1 2 2 3 4 5 6 7 7 53 7243 7251 7259 7267 7275 7284 7292 7300 7308 7316 1 2 2 3 4 5 6 6 7 54 7324 7332 7340 7348 7356 7364 7372 7380 7388 7396 1 2 2 3 4 5 6 6 7 208 Table VIII. — Continued. LOGARITHMS Proportional Parts. Nat. Nos. 1 2 3 4 5 6 7 8 9 12 3 4 5 6 7 8 9 55 7404 7412 7419 7427 7435 7443 7451 7459 7466 7474 1 2 2 3 4 5 5 6 7 56 7482 7490 7497 7505 7513 7520 7528 7536 7543 7551 12 2 3 4 5 5 6 7 57 7559 7566 7574 7582 7589 7597 7604 7612 7619 7627 1 2 2 3 4 5 5 6 7 58 7634 7642 7649 7657 7664 7672 7679 7686 7694 7701 1 1 2 3 4 4 5 6 7 59 7709 7716 7723 7731 7738 7745 7752 7760 7767 7774 1 1 2 3 4 4 5 6 7 60 7782 7789 7796 7803 7810 7818 7825 7832 7839 7846 1 1 2 3 4 4 5 6 6 61 7853 7860 7868 7875 7882 7889 7896 7903 7910 7917 1 1 2 3 4 4 5 6 6 62 7924 7931 7938 7945 7952 7959 7966 7973 7980 7987 1 1 2 3 3 4 5 6 6 63 7993 8000 8007 8014 8021 8028 8035 8041 8048 8055 1 1 2 3 3 4 5 5 6 64 8062 8069 8075 8082 8089 8096 8102 8109 8116 8122 1 1 2 3 3 4 5 5 6 65 8129 8136 8142 8149 8156 8162 8169 8176 8182 8189 1 1 2 3 3 4 5 5 6 66 8195 8202 8209 8215 8222 8228 8235 8241 8248 8254 1 1 2 3 3 4 5 5 6 67 8261 8267 8274 8280 8287 8293 8299 .8306 8312 8319 1 1 2 3 3 4 5 5 6 68 8325 8331 8338 8344 8351 8357 8363 837C 8376 8382 1 1 2 3 3 4 4 5 6 69 8388 8395 8401 8407 8414 8420 8426 8432 8439 8445 1 1 2 2 3 4 4 5 6 70 8451 8457 8463 8470 8476 8482 8488 8494 8500 8506 1 1 2 2 3 4 4 5 6 71 8513 8519 8525 8531 8537 8543 8549 8555 8561 8567 1 1 2 2 3 4 4 5 5 72 8573 8579 8585 8591 8597 8603 8609 8615 8621 8627 1 1 2 2 3 4 4 5 5 73 8633 8639 8645J8651 8657 8663 8669 8675 8681 8686 1 1 2 2 3 4 4 5 5 74 8692 8698 8704 8710 8716 8722 8727 873S 8739 8745 1 1 2 2 3 4 4 5 5 75 8751 8756 87628768 8774 8779 8785 8791 8797 8802 1 1 2 2 3 3 4 5 5 76 8808 8814 8820 8825 8831 8837 8842 8848 8854 8859 1 1 2 2 3 3 4 5 5 77 8865 887118876 8882 8887 8893 8899 8904 8910 8915 1 1 2 2 3 3 4 4 5 78 8921 8927 8932 8938 8943 8949 8954 8960 8965 8971 1 1 2 2 3 3 4 4 5 79 8976 8982 8987 8993 8998 9004 9009 9015 9020 9025 1 1 2 2 3 3 4 4 5 80 9031 9036 9042 9047 9053 9058 9063 9069 9074 9079 1 1 2 2 3 3 4 4 5 81 9085 9090 9096 9101 9106 9112 9117 9122 9128 9133 1 1 2 2 3 3 4 4 5 82 9138 9143 9149 9154 9159 9165 9170 9175 9180 9186 1 1 2 2 3 3 4 4 5 83 9191 9196 9201 9206 9212 9217 9222 9227 9232 9238 1 1 2 2 3 3 4 4 5 84 85 9243 9248 9253 9258 9263 9269 9274 9279 9284 9289 1 1 2 2 3 3 4 4 5 9294 9299 9304 9309 9315 9320 9325 9330 9335 9340 1 1 2 2 3 3 4 4 5 86 9345 9350 9355 9360 9365 9370 9375 9380 9385 9390 1 1 2 2 3 3 4 4 5 87 9395 9400 9405 9410 9415 9420 9425 9430 9435 9440 1 1 2 2 3 3 4 4 88 9445 9450 9455 9460 9465 9469 9474 9479 9484 9489 1 1 2 2 3 3 4 4 89 9494 9499 9504 9509 9513 9518 9523 9528 9533 9538 1 1 2 2 3 3 4 4 90 9542 9547 9552 9557 9562 9566 9571 9576 9581 9586 1 1 2 2 3 3 4 4 91 9590 9595 9600 9605 9609 9614 9619 9624 9628 9633 1 1 2 2 3 3 4 4 92 9638 9643 9647 9652 9657 9661 9666 9671 9675 9680 1 1 2 2 3 3 4 4 93 9685 9689 9694 9699 9703 9708 9713* 9717 9722 9727 1 1 2 2 3 3 4 4 94 9731 9736 9741 9745 9750 9754 9759 9763 9768 9773 1 1 2 2 3 3 4 4 95 9777 9782 9786 9791 9795 9800 9805 9809 9814 9818 1 1 2 2 3 3 4 4 96 9823 9827 9832 9836 9841 9845 9850 9854 9859 9863 1 1 2 2 3 3 4 4 97 9868 9872 9877 9881 9886 9890 9894 9899 9903 9908 1 1 2 2 3 3 4 4 98 9912 9917 9921 9926 9930 9934 9939 9943 9948 9952 1 1 2 2 3 3 4 4 99 9956 1 9961 9965 9969 9974 9978 9983 9987 9991 9996 1 1 2 2 3 3 3 4 209 2IO APPENDIX Table IX REFERENCES ON ENGINEERING THERMODYNAMICS Engineering Thermodynamics. Charles E. Lucke. McGraw-Hill Book Co., New York City, N. Y. Heat Engineering. Arthur M. Greene, Jr. McGraw-Hill Book Co., New York City, N. Y. Applied Thermodynamics. Wm. D. Ennis. D. Van Nostrand Co., New York City, N. Y. Principles of Thermodynamics. G. A. Goodenough. H. Holt & Co., New York City, N. Y. Thermodynamics of the Steam Engine and Other Heat Engines. Cecil H. Peabody. John Wiley & Sons, Inc., New York City, N. Y. Elements of Heat Power Engineering. Hirshfeld and Barnard. John Wiley & Sons, Inc., New York City, N. Y. Thermodynamics. Dr. Max Planck, Alex. Ogg, Trans. Longmans, Green & Co., New York City, N. Y. Thermodynamics. De Volson Wood. John Wiley & Sons, Inc., New York City, N. Y. Technical Thermodynamics. Gustav Zeuner, J. F. Klein, Trans. D. Van Nos- trand Co., New York City, N. Y. Thermodynamics of Heat Engines. Sidney A. Reeve. MacMillan Company, New York City, N. Y. An Introduction to General Thermodynamics. Henry A. Perkins. John Wiley & Sons, Inc., New York City, N. Y. Thermodynamics of Technical Gas Reactions. Dr. F. Haber. Longmans, Green & Co., New York City, N. Y. The Thermodynamic Principles of Engine Design. L. M. Hobbs. C. Griffin & Co., London. An Outline of the Theory of Thermodynamics. Edgar Buckingham. MacMillan Company, New York City, N. Y. The Temperature-Entropy Diagram. Charles W. Berry. John Wiley & Sons, Inc., New York City, N. Y. The Steam Engine and Other Steam Motors. Robert C. H. Heck. D. Van Nostrand Co., New York City, N. Y. The Steam Engine and Turbine. Robert C. H. Heck. D. Van Nostrand Co., New York City, N. Y. Steam Engine, Theory and Practice. Wm. Ripper. Longmans, Green & Co., New York City, N. Y. Internal Combustion Engines. R. C. Carpenter, and Diederichs. D. Van Nos- trand Co., New York City, N. Y. Gas, Petrol and Oil Engines, Vol. I. Dugald Clerk. John Wiley & Sons, Inc., New York City, N. Y. Gas, Petrol and Oil Engines, Vol II. Clerk and Burls. John Wiley & Sons, Inc., New York City, N. Y. The Design and Construction of Internal Combustion Engines. Hugo Guldner. D. Van Nostrand Co., New York City, N. Y. APPENDIX 211 Gas Engine Design. C. E. Lucke. D. Van Nostrand Company, New York City, N. Y. Modern Gas Engine and the Gas Producer. A. M. Levin. John Wiley & Sons, Inc., New York City, N. Y. The Gas Turbine. H. Holzwarth. C. G. Griffin Company, London. Physical Significance of Entropy. J. F. Klein. D. Van Nostrand Co., New York City, N. Y. Practical Treatise on the "Otto" Cycle Gas Engine. Wm. Norris. Longmans, Green & Co., New York City, N. Y. Steam Tables and Diagrams. Marks & Davis. Longmans, Green & Co., New York City, N. Y. Properties of Steam and Ammonia. G. A. Goodenough, John Wiley & Sons, Inc., New York City, N. Y. Tables of the Properties of Steam and Other Vapors and Temperature Entropy Table. Cecil H. Peabody. John Wiley ^ Sons, Inc., New York City, N. Y. Thermodynamic Properties of Ammonia. Robert B. Brownlee, Frederick G. Keyes. John Wiley & Sons, Inc., New York City, N. Y. Reflections on the Motive Power of Heat and on Machines fitted to Develop Power. N. L. S. Carnot. Edited by R. H. Thurston, John Wiley & Sons, Inc., New York City, N. Y. Energy. Sidney A. Reeve. McGraw-Hill Book Co., New York City, N. Y. A New Analysis of the Cylinder Performance of Reciprocating Engines. J. P. Clayton, University of Illinois. Univ. of 111. Bulletin, Vol. IX, No. 26. Urbana, 111. 191 2. Thermal Properties of Steam. G. A. Goodenough. Bulletin of the University of Illinois, Urbana, 111. Vol. XII, No. 1. 1914. INDEX Absolute temperature, 3, 15. pressure, 6. zero, 3. Absorption system of refrigeration, 1 Adiabatic expansion, 27, 32, 36, 43, no, 128. compression, 32, 36, 43. lines of steam, 109. Air compressor, 178. engines, 49. Ammonia machine, 191. Apu, 67. Available energy of steam, 128-134. Barrel calorimeter, 84. Barrus' calorimeter, 81, 82. Boyle's law, 15, 29. Brake horse power, 8. Brayton cycle, 57. British thermal unit, 3. Calorie, 3. Calorimeter, steam, 77-85. Carnot, 40. Carnot cycle, 40, 117. cycle, efficiency of, 44. cycle, entropy changes, 94. cycle, reversed, 45. Centigrade, 2, 3. Charles' law, 16. Clausius, 119. cycle, 119. Clayton's analysis, 147. Coefficient of flow, 165. of performance, 194. Combined diagrams, 140. Combination law, 16. Compound engine, 140. Compressed air, 178-185. Compression, adiabatic, 32, 36, 43. Compression, isothermal, 27, 42. of gases, 26. of vapors, 104. 93. Compressor, air, 178. 94, Condensing calorimeters, 84. Conservation of energy, 9. Conversion of temperatures, 2, 3. Cycle, Brayton, 57. Carnot, 40. Clausius, 119. definition of, 40. hot-air engine, 49. internal-combustion engine, 53. Otto, 56. Rankine, 119, 140. reversible, 45. steam engine, 125. Stirling, 50. Density, 65, 154, 198. Diagram, temperature-entropy, 95, 134. heat-entropy, in. indicator, 26, 47, 140. Mollier, 99, 113, (Appendix). total heat-entropy, 1 1 1 , 113. Discharge, maximum, 135. Dry saturated steam, 71. Drying of steam by throttling, 75. Efficiency, air engines, 52, 53. Carnot cycle, 44. Ericsson engine, 53. Rankine cycle, 119, 140. refrigerating machine, 94. Stirling engine, 52. thermal, n, 140. volumetric, 181, 183. Energy, available, 128-134. internal, 21, 35, 69. intrinsic, 69. 213 214 INDEX Engine, Ericsson, 52. compound, 140. hot-air, 49. Lenoir, 53. Stirling, 50. Entropy, 91. diagram, 94-102. of the evaporation, 97. of the liquid, 96. Equivalent evaporation, 85. Ericsson hot-air engine, 52. Evaporation, equivalent, 85. external work of, 67. factor of, 85. internal energy of, 69. latent heat of, 67. Expansion of gases, 26. of vapors, 104. Expansions, adiabatic, 27, 32, 36, 43. isothermal, 27, 28, 42, 94. poly tropic, 112. External work, 67. work in steam formation, 67. Factor of evaporation, 85. First law of thermodynamics, 9. Fliegner's formulas, 155. Flow of air, 155. in nozzles, 150. in orifices, 150 of steam, 167, 171. Foot-pound, 6. Foot, square, 6. Gas constant (it), 18, 22. Gas, perfect, 14, 18. Gram-calorie, 3. Grashof, 168. h (heat of liquid), 66. H (total heat of steam), 68. Heat engine efficiencies, 40-60. of liquid, 66. units, 3. Heat-entropy diagram, 111. Hirn's analysis, 144. Hot-air engine, 49. Hyperbolic logarithms, 31, (Appendix). Horse power, 8. Indicator diagram, 26, 47, 140. diagram, combined, 140. Injectors, 165. efficiency of, 166. Internal energy, 21, 35, 69. of evaporation, 69. Intrinsic energy, 69. Isothermal expansion, 27, 28, 42, 94. compression, 27, 42. lines of steam, 108. Joule's law, 21. v Kelvin, 21. L (latent heat of steam), 67. Latent heat of evaporation, 67. Laws of perfect gases, 18. of thermodynamics, 9. Logarithms, natural, 31, (Appendix). "common" or ordinary, 31. Losses, turbine, 163. Mean specific heat, 74, 75. Mechanical equivalent of heat, 8. Moisture in steam, 72, 77. Mollier diagram, 99, 113 (Appendix). Naperian logarithms, 31, (Appendix). Napier's formula, 168. Natural logarithms, 31, (Appendix). Non-expansive cycle, 127. Non-reversible cycle, 45. Nozzle, flow through, 150. Nozzle losses, 173. Nozzles, impulse, 162. reaction, 164. Orifice, flow through, 150. Otto cycle, 56. Per cent wet, 72. Perfect gas, 14, 18. INDEX 2I 5 Porous plug experiment, 21. Power plant diagrams, 100. Pressure-temperature relation, 16, 36. units, 6. Properties of gases, 197. of steam, 63. of vapors, 62. g, 66. Quality of steam, 72, no, 113. R (thermodynamic or "gas" constant), 18, 22, 48. r, 67. Rankine cycle, 119, 140. Ratio of expansion (r), 30. of specific heats, 23, 154. Receiver method, 158. References, 198. Refrigerating machines, 40, 178. media, 87. Refrigeration, applications of, 178. unit of, 187. Regenerator, 51. Reversibility, 45. Reversible cycle, 45. Saturated steam, 62, 65. Saturation curve, 142. Scales, the rmo metric, 2, 3. Second law of thermodynamics, 9. Separating calorimeter, 82. Small calorie, 3. Specific heat, 4, 23. heat at constant pressure, 5, 197. heat at constant volume, 5, 197. heat, instantaneous values of, 76. heat, mean value of, 75. heat, ratio of, 23. heat of gases, 197. heat of superheated steam, 75, 76. heat of water, 4. volume of gases, 6, 198. volume of saturated steam, 65. volume of superheated steam, 75. Steam, dry, 71. Steam engines, efficiencies of, 119. engines, power plant, 100. entropy for, 96. saturated, 71. superheated, 72, 73. tables, (Appendix). total heat of, 68. turbine, 163. wet, 71. Stirling engine, 50. Superheated steam, 72. Superheating calorimeter, 77, 132. Symbols, ix, x. Tables, steam, (Appendix). vapor, 63. Temperature, absolute, 3. -entropy diagrams, 95-102, 134. -entropy diagram for power plant, 100. Thermal efficiency, n, 140. unit, British, 3. Thermodynamics, definition of, 1. Thermo metric scales, 2, 3. Throttling, 75. Throttling calorimeter, 77, 80, 81. Total heat-entropy diagram, in, 113. heat of saturated steam, 68. heat of superheated steam, 73. internal energy of steam, 69. Turbine, steam, 163. Under-expansion, 173. Unit of heat, 3. Vaporization (see evaporation). Vapors, 62, 104. properties of, 62. Velocity, 155. Volume, specific, 6, 65, 75, 198. Volumetric efficiency, 181, 183. Water, specific heat of, 4. Watt, 8. Weight, units of, 3 (footnote). Wet steam, 71, no, 131. 2l6 INDEX Wetness of steam, 72. Wire-drawing, 75. Work, external, 6, 67. of adiabatic expansion, 67. of Carnot cycle, 44. of Clausius cycle, 120. Work, of compression, 179. of Rankine cycle, 120. x (quality of steam), 72, no. Zero, absolute, 3. TOTAL HEAT-ENTROPY DIAGRAM. The ordinates are Total Heats. The abscissae are Entropies. Vertical lines are lines of constant entropy. Horizontal lines are lines of constant total heat. Reproduced by permission from Marks and Davis' Steam Tables. S 178 1.82 i.fls 1.90 J □ 1.M 1.88 wer Plant Engineering." EqnlT. Velocity Ft. lb«. B.T.U. Ft. per of Work second " . 1300 — — :— 6oo' _ — 1000 I — Z - 60 " ErlMO' soooo" Z ~ =- - — =-2000' - ioo- =- = . 100000 5-2600' E. " 160 " ZT" — — — i — — — =^■8000' 16001)0 - 200~ = — — — k " 260 ~ —8500' 200000 - — — jam. JUL 35000oT-460 -fc r Moli n r Chart Reproduced by permission from Gebhardt's " Steam Power Plant Engineering.