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Mee 216 Continuation

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Mee 216 Continuation

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Basic Concepts and Laws of Thermodynamics // 75 Upon solutién Q) = 312.5 kJ/min (from source at 600 K) 2 = 1000 ~ 1.6 x 312.5 = 500 kj/min _ (from source at 800 K) @ = 06 Q, = 3125 « 06 = 1875 Kj/min (from source at 1000 K) E: ENTROPY 1.27. WHAT IS ENTROPY ? From Clausius theorem, the cyclic integral of the quantity 80/'T for a reversible process is zero “his suggests that the quantity 5Q/Tis a point function and hence a property of the system. This Property is called entropy (denoted by §) and its change from initial equilibrium state 1 to final equilibrium state 2 during a reversible process is (22). =Jor-s-5, say 1 = 4. Entropy is an extensive property as it depends on the mass of the system. The unit of entropy is kJ/K while that of specific entropy (entropy per unit mass) is kJ/kg K. The entropy of a system increases with absorption of heat and decreases with heat rejection. For a reversible adiabatic process 6Q = 0 and so will be the entropy change. Thus it may be stated that entropy is a property of the system that remains constant during a reversible adiabatic process. The reversible adiabatic process during which entropy remains constant is called isentropic process. However, an isentropic process need not be an adiabatic process as the entropy during a particular process may be kept constant by heat transfer-to or from the system. Essentialy entropy is a measure of the degree of randomness of the molecules comprising the system. Higher the disorder, greater is the increase in entropy. 1.28. ENTROPY IS A POINT FUNCTION Consider a system taken from initial state 1 to final state 2 by following the reversible path A. Subsequently the system may be brought back to initial state by following the reversible paths B or C. The paths A and B together constitute a zeversible cycle and so do the paths A and C. Then in accordance with Clausius theorem ia 1 vin B 20 50, 50 A 1 7 oft g a 278450 50 no é 60 F F t 1 2 | Ga (52) en by §Q dS> |“ Hence, for the general case, it may be stated that 8Q 15 ds > 82 3) S 2 or 5,-5, 2f2 (143) The equality process. The equation 1.43 shows that entropy i ° ; j . served (remains constant) during a reversi NG an itteversible process and is com (whether reversible or irrev 0 ‘ and, therefore, change is zero in a reversible adiabati 2 r oe iabatic process, and greater th; i 1 sign holds good for a reversible process and the inequality sign for an irreversible lat for an adiabatic process 4S 2 0. This implies that entrop! ‘2n ero in an irreversible adiabatic 1.30. ENTROPY PRINCIPLE _ “Entropy of an isolated sys An isolated system d surroundings, and the total system (80 = 0), item either increases it or, in the limit, remaiy » remains constant, ” loes not undergo an nt. energy ofall postbie ne' 8 (work or heat) interaction with thé *Femains constant. Therefore, for an isola! (as), > 0 For a reversible process : (45),,, = 0 or S For an irreversible process : (dS) aay = constant iso” 0 oF entropy increases Basic Concepts and Laws of Thermody a eencepts and | Thusit may b single boundary. The isolated 5 affected by the process, Refer to the isolated system, consisting of its surroundings, as shown in Fi occurs irreversible transfer of a system and 8-146. If T,.>T,.,, there heat from the syste: to the surroundings. (as), « 282 ere a . entropy principle 3Q ds). = 22 (San = 5 Therefore, entropy change for the isolated system or surroundings is (S)ig = (dS),y, + (dS), 1 1 = 6Q}——-— (1.46) | " Z| s Since T,,, is less than T,,, = We can write (ds);., > 0 That s the entropy of an isolated system increases if the isolated system undergoes an irreversible Process. Incase T.,,=T.,,, the process would occur reve rsibly and the entropy will remain constant Thus we may generalise and state that system, Since the universe is an ‘solated system and all real processes are irreversible, the entropy of the universe must be increasing, Thus it is an age of entropy growth progressively and the entropy of the world ten. maximum ids towards a 1.31. TEMPERATURE - ENTROPY PLOT When a system is taken, reversibly from initial state 1 to final state 2, 2 Qyey = J TUS 1 This implies that the area under Tepresents the quantity of heat int tis to be noted that : acurve for a reversible process plotted on T—S co-ordinates ‘eraction during the process. reversible adiabatic ~ During a reversible adiabatic process, 6Q=OandsoS= constant is a ve Process is represented by a vertical (constant entropy) line on T~ § diag F aa : erefore, ~ During a reversible isothermal process, T = constant and, therefo 2 Qo = FFAS = T (S,~ $4) 1 78 || Basics of Mechanical Engineering _ —— , y a horizontal (constant tempera The reversible isothermal process is represented by a hori tg on T=S diagram, 7 T T Adiabatic process eel 1 >S 2 ob------ S, ele & a Fig, 1.47. Temperature entropy plots Recapitulate that a Carnot cycle consists of two reversible isothermals and two reversipy acliabatics. Accordingly a Carnot cycle would plot as a rectangle on TS diagram, Process a ~ b: Isothermal expansion at constant temperature T, during which heat Q, is ‘Suppl: to the system, Q, = area under the process line a—b = T,dS Provess bc: Adiabatic expansion during which work is done by the system, Process ¢-d : Isothermal compression at constant temperature T, during which heat Qi rejected by the system, y = area under the process line c—d = T, dS Processi—a: Adiabatic compression during which work a oA is done on the system n a Efficieney of Carnot cycle, n= Workdone percyele _ Q,-9, 1 heat supplied per cycle ~~ @, _TdS-Tds T,- 1! ¢ vale ec oS . U Uhcates of therectangleabed represents the work a out per cycle and it equals, an See Q-Q =(T,-7,) a5 Fig, 1.48. Carnot cycle EXAMPLE 1.69 ; undergoes a reveraible proc ing which’ f . ess at 500 K di whic receives 0.75 M) of heat. Determine the inereres in specific eattone of the eet wot the system for the same initial and final states be affect® ble (ii) heat supply hy; ly had by Solution : Heat supplied per kg of fluid, s cen doubled, 0.5 MJ = Su iy | _ 89 500 change in entropy, dr = > = 500 71 ki/kg k . Basic Concepts and Laws of Thermad Entropy, like any other property, is dependent entirely upon th independent of the path or heat supplied to achieve that state. Ther irreversible and the heat supply is doubled, the change in spe 1KI/kg K. of the system and is vif the proces temperature, Solution : Refer Fig. 1.52, From the correlation: 84 = T ds Heat flow = area under the line air = base x mean ordinate “ 1 H = (4.25 ~ 4) x = (280 + 360) 4 c 2 ( 4 425 S 0 KI/kg Fig. 1.49. Total heat flow, 8Q =m &q=5* 80 = 400 kj EXAMPLE 1.71. A heat engine c Solution : Refer Fig. 1.53 One cm? of area on T—$ plane is a measure of =100*0.1=10Kj Area on T—S diagram represents heat transfer accordance with first law of thermodynamics §eo = gow and in fherefore, the cyclic area on T~S diagram gives the sel work output | * Work output per cycle = area of the circle abed 1 ° ® , = = 4mem? = 4x «10 = 40m kj} Fig. 1.50. Power developed = work don '¢ per second = 40x x 10 = 400n KJ/s = 1256.6 KW Heat supplied, Q, = area under abe = area abe + area acef A(x | 2 =5|Z*4 |4+5x4 = n+ 20) cm AE (2x + 20) Qn + 20) x 1 area under cda Heat rejected, Q A(x ) ema = -s{4x4?] = (20-20) em = 5x4 i{Ex t = (20 - 2m) x 10 = 137.2 kI/eycle 80 // Basics of Mechanical Engineering Thermal efficiency of engine, 262.8 - 137.2 = 0.478 or 47.8% 262.8 EXAMPLE 1.72, Heat flows from a reservoir at 800 K to another reservoir at 250 f entropy change of the ha reservoir is - 4 kJ/K, determine the entropy change of the cold reservoir. Q Solution : Entropy change is defined as, dS = == z- Heat lost by the hot reservoir, Q = T dS = 800 (- 4) = - 3200 kJ ‘An equivalent amount of heat is received by the cold reservoir. +. Entropy change of cold reservoir, 3200 = Sep 128k) = EXAMPLE 1.73 Heat flows from a hot reservoir at 800 K to another reservoir at 250 the entropy change of the overall proces is 4.25 kV/K, make calculations for the heat flowing out of the high temperature reservoir, Solution : Let Q be the heat that flows out of the hot reservoir. An equivalent amount will be the heat received by the cold reservoir. For the high temperature reservoir, (48), For the low temperature reservoir, (dS), = Q) t Net entropy change, (4S), = (48), + (dS), -72, 2 425 = soy a5} Q= 1545.45 kg EXAMPLE 1.74, A Lump of ae es f is at 1000 Kis dropped in 80 kg of oil at 300 K. Make calculations se of steel, i i iii osuyng sangeet sumeiland the universe. Take specific heats of steel and oil as Solution : Let Tbe the final equity 7 equilibrium temperature. Then fr iple bet ety ea © One Principle of energy conservation (6,47 see 805 x (1000-7) = 80 x3 j Entropy change of steel, T, i £ (5g * eB . 309.86, + 8% 0.5>log, 0.86 == A686 yk Basic Concepts and Laws of Thermodynamics // 84 i Entropy change of oil, (dS),,, = me, loge A = 80x3, ae 3.5 x log, = 9.0547 kj/K + Net change of entropy (i-e., entropy change of universe) is, (48) criverse = (AS) sti * (AS), = - 4.686 + 9.0547 = 4,369 kj/K (increase) 309.8¢ 300 EXAMPLE 1.75. Ina certain heat exchanger, 50 kg of water is heated per minute from 50°C to 110°C by hot gases which enter the heat exchanger at 250°C. If the flow rate of gases is 100 kg/min, estimate the net change of entropy. Sp (water) = 4.186 ki/kg K; ¢, (gas) = 1 kI/kg K Solution : Assuming no loss of heat to surroundings, the principle of energy conservation gives, heat lost by gases = heat gained by water (AT) gas = (MC, AT) water 100 * 1.0 x (250 ~ t,,) = 50 x 4.186 (110 - 50) +. Final temperature of hot gas, t,,= 124.42°C T, Entropy change of gases, (45)... = mcy log, oi i 124.42 +273 = .0 log, = - 07.46 1d /ky 100%1.0 log, J/kg Entropy change of water, (AS) yar = MC, tog, 22 ‘el 110 +273 = 50x 4.1861og, ~~ = 35.66 KJ/ky 50x 4.186 0g, 73 = 35.66 K]/kg Net change of entropy, (dS) n) = (4S)zo,* (49), =~ 27.46 + 35.66 = 8.2 kI/kg EXAMPLE 1.76 | \ A hot iron forging (specific heat 0.5 kJ/kg K) weighs 30 kg and has a temperature of 500°C. The forging is dropped into 200 kg oil mass (sp heat 2.5 kJ/kg K) at 25°C for quenching. Make calculations for the entropy change of forging, entropy change of oil and entropy change the composite system. It may be presumed that there is no Joss of heat to the ear Solution : Let suffix f and’o represent the forging and oil respectively. From the princip! energy conservation, { heat lost by the forging = heat gained by the oil myo(Th, = Ty) = ty Cy (Ty ~ Toy) where T,, is the common temperature of the composite system Ty, = 500+ 273 = 773K T,, = 25 +273 = 298 K+ net water 82 // Basics of Mechanical Engineering ; T,,= 311.83 K 30 x 0.5 (773 - T,,) = 200 * 2.5 (Ty, - 298); T= 31 311.83 773 Entroj e of forging = 7 Jn = - 13.617 kJ/K i f forging = my Cy loge 7 = 30x 0.5 loge 13. S/) (0) py change of forging T, 311.83 Tw = = 22.682 kj/K (ii) Entropy change of oil = "Cv !OBe 7p = 200 x 2.5 log. Fog (iii) Change in entropy of the system is (€S)guten = (45) orgng * @5)o = - 13.617 + 22.682 = 9.065 kJ/K (increase) EXAMPLE 1.77. 5 kg of water at 30 °C is mixed with 1 kg of ice at 0 °C. The process of mixing is adiabatic ang the system is open to atmosphere . Make calculations for the temperature of mixture and the change of entropy for the spontaneous mixing process. Take specific heat of water = 4.187 kJ/kg K and latent heat of ice = 335 kJ/kg. Solution : Let T,, be the temperature of the mixture after adiabatic mixing. From the principle of energy conservation, heat lost by water = heat gained by ice 5 x 4.187 (30 - £,,) = 335 + 4.187 (t,, - 0) ; f,, = 11.67°C. (i) Change in entropy of water is given by (4S),sater = entropy change due to cooling of water from 30°C to 11.67°C I, 11.07 +273 = me,!0Ber = 5x 4.187 log, "=" = 1.3004 /K mnej}9Be, = 5% 4.187 log, / (ii) Change in entropy of ice is given by (aS)... = entropy change due to melting of ice at constant temperature + entropy change due to heating of ice water from 0°C to 11.67°C = a veg. 35 11.67 +273 =75 44 " = c 273 * 1X 4-187 log, 273 = 1.4024 KI/K (iii) Change in entropy of the system is (4S)sytom = (A)eater * (lS)ic ~~ 1.3064 + 1.4024 = 0.096 Kj/K (increase) EXAMPLE 1.78. A block of mass m, , specifi another block of correspon ic heat c, and temperature T the process of thermal equi | a is brought into thermal contact wit! ‘ding parameters m,, cyandT, ‘libri. Show that the e ii ij librium is necessarily positive, at he change in entrogy Solution: Let it be presumed that initially the bl lock A is at a hi er 2, ie, T, > Ty & Such the block A will ose heat which will be taken up by the tiene mere i, Ty > Th energy conservation, lock B. ‘Then from the principle ¢ heat lost by block A = heat gained by block B =m, ¢, dt, = my cy dt, Basic Concepts and Laws of Thermodynarn The negative sign stems from the fa ct that dt, is negative, Overall entropy-change, dS = 45 + 4s, MCadta | mycpdty . a ib The terms ( change is positive. EXAMPLE 1.79. 1 kg of water at T, is isobarically and adiabatically mixed with my kg of water at T; (T, > T,). Show that for equal masses of water, the entropy change of the mixture is given by T4T, (4S) mnigerse = 2G og.) 12 ¢ 8 2 [ily and prove that the change is necessarily positive. Solution : Let T, conservation, be the final temperature of the mixture. Then from the principle of energy heat lost by m, kg of water = heat gained by m, kg of water Gy (Ty = T) * 96 (y= Ty) T, + mT or Ty tt my + my Change in entropy of 1m, kg of water, whose temperature decreases from T, to T,is mT, + mT, (my + my)T; Change in entropy of m, kg of water whose temperature increases from T, to Tyis yt ' (45), = mt, log. se = mc loge 1 mT, + pT, Ty + yTy T 5 Le (aS), = mye, log, mn og. (im + Ty *: Change in entropy of universe is mT, + mT (im, +), , iverse takes the form {fm = my =m, then the above expression for change in entropy of universe takes the forn +h T+T +e, log. 27, 8 oT, = a = m6 | ingTy + mT; (in + my (45) sniverse = (dS), + (dS).= me, log, + my loge (45) universe = ™ 1OBe 84 // Basics of Mechanical Engineering T+h] bog, 242 A 5 08, = mG oe 2g, 108.5 TET, which is the required expression. T+h 2 sii greater than geome, The term represents the arithmetic mean and this is always grea Beomety, T+h i ositive and as such the ¢! mean represented by T,T, . Accordingly the term log, s pi hay, isi ing. in entropy is always positive, ie, the entropy of the universe is increasing, EXAMPLE 1.80. - A heat engine operates between two thermal reservoirs; source at temperature T, and sink, temperature T,. If the source and sink are of mass m and specific heat c, set up the followin, expression for the maximum work output possible W rae = 0 € (NT, - VT)? Solution : For maximum work output or maximum efficiency, the heat engine must be reversity 3 co and for a reversible cycle engine; Clausius equation gives se = 0. This implies that entrop change for a reversible cycle is zero. Let T,, be the common temperature when the working of the engine stops. Then, (4S) source * (45) sing = 0 Ty Tn me loge s+ mclog, 2 = 9 TT [Sou 1 b Q, mos tog) a 1 W+—{(_) Heat engi 2 me log. = g Th yo Ty? ToT, se log. —" =g9= 2 BT 70 log. ret ig. 1.51. 2. fe TNT or Ty = Ji Now, work done = = heat supplied ~ heat rejected “me(T-T,,) me (Ty, = T,) “Me = me VT -mels ~1 = me[T, +7, WTB] = me ( ANGE DURING A p| ty, motion, electtici Vt ~ Jey In the absence of gravi can be expressed as Basic Concepts and Laws of Thermadynarnics // 88 8q = du + Bw for unit mass of substance Further if the process is reversible ; 8w = p dv (84),ep = du + p dv From the definition of entropy : Tds = (89),,,, and, therefore, Tds =du+pdv (i) Also, h=utpo dh = du + pdv +vdp and thus Tds =dh-vdp (ii) Expressions (i) and (ii) can be used to work out the entropy change during any process ; whether reversible or irreversible. 4.32.1. Constant Volume Process : For unit mass of subsiance or or Fig. 1.52. T-s diagram constant volume process (1.46) 4.32.2. Constant Pressure Process For unit mass of substance or or Integrating both sides, we get hic ec if fas =S| 1 1 8 2 Th a Fig. 1.53. T-s diagram 69751 = Gp lOBege= SIBeG (AT) oe Sr pone 1 1.32.3. Isothermal Process iy For unit mass of substance 8 = du + pdv te Since the temperature remains constant, du = Qand thereto! 8q =p dv 86 // Basics of Mechanical Engineering yp dv 4 Pw e Re °F Tan, 2 do ds=R2 or is= Ro Integrating both sides, we get A 24 Jas = JS lo 1 2 827, = Rog. Rog. (1.48) Fig. 1.54. T-s diagram: ° a isothermal process Thereversible isothermal processis represented by ahorizontal (constant temperature) line on the T-s diagram. 1.32.4. Reversible Adiabatic (Isentropic) Process During an adiabatic process, heat is neither supplied to or rejected by the system. This shows that the entropy remains constant during.a reversible adiabatic process, and the process is represented by a vertical (constant entropy) line on the T-s diagram, ‘The reversible adiabatic process is known as isentropic process. 1.32.5. Polytropic Process For unit mass of substance $1 = 82 Fig. 1.55. T-s diagram Adiabatic process 8q = du + pdv=c,dT + pdv aT or 2 co + Bao aT dv a Tre rds wea Re : ‘Upon integration between the initial and final states 2 2 aT pay ds = cy fT, (ae J IF +R f ; . b Fig. 1.56, T-s diagram ¢, log, 7, * Rog. a (1.49) Polytropic process This is the expression for entropy change in t cra ee ¥ change in terms of temperature and volume and change * Equation 1.49 can be recast as 2 Basic Concepts and Laws of Thermadyr = cylog. 2 + ¢, log.” + R log”? Pi 80, Bo, Pr v; clog, 2 + (R + 6,) log, 2 Bp, *(R + 6) log. = P2 2 5 = clog 22 + ¢ log. 2 (1.50) Bp, * ple This is the expression for entropy change in terms of pressure and volume. « Equation 1.49 can be recast as I nN =, +R) log.= + R log, 2 ot R)logag? + Rlog. =c log. 2 A = Gplog.ge + Rog, 1.51) This is the expression for entropy change in terms of pressure and temperature. Constant volume and constant pressure lines on T~S diagram For unit mass of substance, the entropy changes are aT ds = oor for constant volume process, and ds = ¢,“ for constant pressure process Ly s \& Gy Bde ~ Fig. 1.57. Constant volume and constant pressure lineas on T-S diagram Therefore, slope of the constant volume line on T~ S$ diagram, ar tT ' mines Fig. 1.58, Two reversible adiabatics intersecting each ather a 88 // Basics of Mechanical Engineering And slope of the constant pressure line on T—$ diagram aT T “i sty Since ¢,> ,, the above expressions indicate that constant volume line on T~ $ diagran, ; ~ ey & t steeper than constant pressure line wotking between the same temperature limits. Further, ce ¢, and ¢, are constant 2) «T both for the constant pressure and constant volume Processes Can two reversible adiabatic paths intersect each other : : For a reversible adiabatic process, heat interaction is zero and so is the change in entra (dS = 8Q/T). Two constant entropy curves S, and S, have been depicted onp-v diagram. IF we assume that these curves intersect at point A as shown, then at the point of intersection, there wil be two values of entropy. However, entropy is a property and point function, and cannot have two values at any point. Further, let a reversible isothermal be plotted of the p—v diagram and let it intersect the reversible adiabatics at B and C. The reversible processes AB, BC, CA then constitute a reversible cycle. The included area ABC represents the net work output. However, this work has been obtained from an engine which exchanges heat with a single thermal reservoir during the isothermal process BC ( there is no heat intraction during the adiabatics AB and CB). This is im violation of the elvin-Planck statement of the second law. Hence, our assumption of intersection of two reversible adiabatics is wrong, Through one point, there can pass only one reversible adiabatic. EXAMPLE 1.81 7 A rigid cylinder containing 0.005 m? of nitrogen (molecular mass 28) at 1 bar and 290 K is heated reversibly until the temperature becomes 360 K. Determine the heat supplied and entropy change. Assume nitrogen to be perfect gas and take y=14, t Solution : A rigid cylinder implies that the heating of the gas is done at constant volume. Reig Gas constant, R = ———wla__ 8314 molecular mass ~~ 9g ~ 196.93 J/kg K therefore, es ? 1x 10° x 0.005 a - 296.93 x 299 ~ 5.806% 10 kg, 296.93 ay. [ary 774232 J/kg k Heat supplied = me,(T, .'r,) : — =.5.806 x 10-3 x 742.39 (360 - 290) = 301.694 = 0,302 Ky Change in entropy, (5, - 5.) = me,log, & “ 1 = 5,806 x 103749 32log, 360 290 = 0.9319 kg K = 0.932 x 193 ki/kg K L Basic Concepts and Laws of Thermadynamics // 89 EXAMPLE 1.82 _ A piston-cylinder arrangement contains 0.03 m3 moves inwards and the gas is compressed isotherm 4 bar. Determine change in entropy and work d of nitrogen at 1 bar and 290 K. The piston ally and reversibly until the pressure becomes lone. Assume nitrogen to be a perfect gas. :Gas constant, +R = ——Rma _____-8314 politics molecular mass ~~g = 296.93 J/kg K Pim _ 1x10° x 0.03 m 0 «0.03 _ T, 296.98 «290, ~ 9.03484 ke For an isothermal process, the change in entropy is given by 0 . (S-S,) mRlog, 2 =mRlog, P= 0,03484 x 296.93 log, i p 1 ” ~ 14.341 J/K = - 0.01434 KJ/K (Sy - $,) = 290 x (- 0.01434) = - 4.1586 KJ During an isothermal process, work done equals the heat interaction Work done = - 4.1586 ky Heat interaction, Q 2, 5 Alternatively, Work done = Pi? log, => = piv, log, 2 = 110° x0,03lo: 1 2 = - 4158.88 J = - 4.1589 kJ ply Be 4 EXAMPLE 1.83. A piston-cylinder arrangement contains 1 kg of air at pressure 1 bar and temperature 300 K. When 10 kj of work is done on air, its parameters change to 2.5 bar and 310 K. If the piston - cylinder assembly exchanges heat only with a reservoir maintained at 300 K, make calculations for entropy change of the air, entropy change of the reservoir and heat transfer from the air. Comment on the truth or falsehood of the claim. For air ¢, = 1.005 k]/kg K and R = 0.287 ki/kg K Solution : In terms of pressure and temperature, the entropy change is I, PL S,~ S, = me, log. 22 + mR log, ZL ao een, Pr = 131.005 log, S20 +1 x 0.287 log, oF = 0.03295 - 0.26298 = - 0.23 kJ/K aU = mc,aT = m (c, - R) dT = 1 (1.005 - 0.287) (310 - 300) = 7.18 kj} From principle of energy conservation, 8Q = dU - 8W=7.18 - 10 = - 2.82 k] | This heat transfer out of the air is received by the reservoir, and therefore, entropy change for the reservoir is = 0.0094 kJ/K 90 // Basics of Mechanical Engineering Overall entropy change = (d5)qi, + (48)yesercoir = 025 +0008" -022061/ impossible and as But negative entropy change for a composite system (universe) is imp e *Stchy claim is false. 1.33. THIRD LAW OF THERMODYNAMICS (NERNST TAM) upon its temperat ivi bstance depen« ure 5 f atomic or molecular activity of a sul : esl he res fre oe ea becomes equal to zero. This is the essence of third law of thermody: pane ; es the “At absolute zero temperature, the entropy of all homogeneous crystalline (condensed) suf stances, 4 state of equilibrium becomes zero.” . i t When expressed mathematically : dt $=0. This implies that at absolute zero temperaty, the entropy ceases to be a function of state and approaches a constant value independeyy oft Parameters ofthe state, However, for many substances like alloys, all amorphous bodies, cheng compounds CO, NO ete,, the entropy does not tend to zero as T — 0, but takes a finite posi, value. This is because these substances are not found in equilibrium state. The third law provides an absolute base from which the entropy of each substance cany measured. The entropy relative to this base is referred to as the absolute entropy. Further, is Jaw is helpful in _ Measurement of chemical affinity, ie, the action of chemical forces of the reacting substance ~ explaining the behaviour of solids at very low temperatures. — analysing the chemical and phase equilibrium. REVIEW QUESTIONS A. Conceptual and conventional questions : Define system, boundary and surrounding, 2. Explain the concept of close : d system, an open system and an isolated system. Give suitable examplest illustrate your answer. ‘What is meant by thermodynamic equilibrium? Give thermodynamic definition of wor What is a perfect gas? Enumerate the Define the characteristic gas constant, these constants, Kk. What is positive and negative work? loss of perfect loss How does it difer from universl gas constant? Write the unis # lar mass is same! ee » Write its mathematical expression for, 11. 12. process and acyclic pros 13. (a) State the second law of () Prove the equivaince thermodynamics. Basic Concepts id Laws of The: {u) What the processes involved in a Carnot cycle 7 (i) Derive an expression for the thermal efficiency of a Carnot eyck 15, Name and define the property that remains constant during a reversible adiabatic procs 16 What expression for heat tranfer is equivalent to the term p dv for work wanster? 17, What does the principle of entropy increase, specify? 8a \ 48. show that whenever a system executes a complete cyclic process, is js less than ze70 or int js equal to zero. Hence, prove that entropy is a property of the system. . Hill in the blanks with appropriate word/words 1, Asystem is separated from its surroundings-by a system exchanges neither mass nor energy with another syste which may be sce OF m or with the surroundir 2 3, _ property of the system remains the same whether one considers the whole system oF 2 4, The state is the condition of a system identified by its 5, Zeroth law of thermodynamics forms the basis of ....-..n+ measurement 6. First law of thermodynamics refers to conservation of . 7. Inthe context of a closed non-flow system, the difference between heat added to and work done by the system equals the change in 8. As per the essence of 9, Refrigerators and heat pumps are 40, The processes involved in a Carnot cycle are two . Taw of thermodynamics, no engine can be 100 percent efficient sy heat engines. onun Processes and two processes. Answers: . 1 boundary, rigi, flexible; 2. an isolated; 3, intensive; 4. thermodynamic properties; 5. temperature; 6. ners 7 internal energy; 8. second; 9. reversed; 10. adiabatic, isothermal. C. Multiple choice questions: 1. A thermodynamic system refers to (@) any defined region in space (B) a specific mass in fluid flow (©) a specified region of constant volume (@) a prescribed and identifiable quantity of mat! 2. A system and its environment put together constitute (@) an adiabatic system (b) an isolated system (©) a segregated system (a) a composite system 3. Which of the following represents a closed system ? (®) bomb calorimater (W) boiler (0) universe (@ centrifugal pumy gal pump 4. The value of an extensive property is essentially dependent on (a) mass or extent of the system (b) nature of boundaries, rigid oF flexible (0) path followed by the system in going from one state to another (a) interaction of system with the surroundings. 5. Which one of the properties given below is an extensive property of the system ? (a) pressure (b) temperature (©) volume (a) density 6. Which amongst the following is not a property of the system ? (a) heat (b) composition (0) specific volume (d) thermal conductivity 4 92 // Basics of Mechanical Engineering 7. Choose the correct statement (a) temperature is an extensive property (©) the system boundaries may expand or collapse (@) an isolated system allows exchange of energy © ° 8. Which of the following statement does not represent the essence of the eat law of thermodynan, (@) heat input to a system equals the network done plus change in internal enetBy (B) the sum of heat and work inputs will be zero if the system undergoes a cycle (©) heat input cannot be more than the work output (d)_ for an isolated system, energy remains constant. 9. Heat cannot be transported from a system at low temperature to a system at high temperature wig the aid of external agency. —_ This statement of second law of thermodynamics is attributed to (a) Sadi Carnot (® Clausius (c) Kelvin-Planck (d) Joule-Thomson 10. For a heat engine operating in Carnot cycle, the work output is ¥ith of heat rejected to the sink 7, thermal efficiency of the engine would be (@) 10% (&) 20% (9) 30% (@ 50% 11. If the thermal efficiency of a Carnot heat engine is 40 percent, then coefficient of performance of, refrigerator working within the same temperature limits would be (b) mass remains same in an open syste ynly in the form of heat. (@ 15 () 25 (35 @45 12, Zeroth law ; temperature :: second law (a). internal energy () entropy (© enthalpy (@) availability 13. During an isothermal process, change occurs in (a) pressure (6) temperature (0) pressure volume (@) internal energy 14. The third law of thermodynamics (a) defines internal energy (H) provides a base from which entropy is measured (©) gives availability of heat for conversion into work (d) decides whether a process is reversible or irreversible. 15. Which amongst the following gases has the lowest value of characieristic gas constant ? (@ Hydrogen (b) Nitrogen (Q Air (d) Carbon dioxide 16. Consider the following properties of a thermodynamic system (a) Kinematic energy (6) thermal conductivi Which of these are intensive properties : EN aie (a@) land 2 (b) 2and3 () 2.3 and4 (@) 1,3 and 4 17. Two blocks which are a differe (2) Zeroth First 18. The entropy of universe (@) is always zero (0) tends to be minimum (©) tends to be maximums (4) remains constant at a certain finite value Answers: : ae a O ne {9° 30 6 ® 7 15. (d) 16. (c) 17. @) 18. HH 5 12. 0) 13. €@) v4. eh D, State True of False. If false write the 1 Basic Concepts and Laws of Thermodynamics // 83 correct statement : A closed thermodynamic system is one in which there is no energy bar or mass transfer across the boundary. 2. A real gas obeys perfect gas laws at very high temperature and pressure conditions. 3, Mole is a unit of mass. 4. Internal energy of an ideal gas is a function of temperature alone 5. Change in enthalpy in a closed system is equal to heat transferred if the reversible process takes place at constant volume. 6 Internal energy of a substance does not include any energy that it may possess as a result of its macroscopic position or movement. 7, All constant entropy processes are adiabatic, but all adiabatic Processes are not isentropic. 8 The sum of entropy of all the bodies taking part in a process always increases. 9. COP of a heat pump is less than COP of its refrigerator version. 10. Assigning the basic dimension to mass, length, time and temperature respectively as M. L, T and 0, the dimensions of entropy are META gt Answers: 1 False, no mass transfer but energy transfer exits; 2. False, high temperature and low pressure; 3 False, A 22.41 m® of volume is known as mole. Obviously mole is a bigger unit of volume 4. Trae; 5. False; constant pressure; 6. True; 7. True; 8. True; 9. False, (COP) pup = (COP) ep + 1; 10. False, entropy = ——tet energy MET? ao ga temperature temperature 0 E. Each of the next items consists of two statements, one labeled as the Assertion (A) and the other as Reason (R). You are to examine these two ‘statements carefully and select the answers to these items using the codes given below: Codes: (a) Both A and R are individually true and R is the correct explanation of A (b) Both A and R are individually true but R is not the correct explanation of A (c) A is true but R is false (d) A is false but R is true 1. Assertion (A): A thermodynamic system may be considered as a quantity of working substance with which interactions of work and heat are studied. Reason (R) : Energy in the form of work and heat are convertible, 2. Assertion (A): The change in heat and work cannot be expressed as difference between the end states. Reason (R) : Heat and work are both exact differentials, 3. 5. Assertion (A): Specific heat at constant pressure for an ideal gas is always greater than the specific heat at constant volume. Reason (R) : Heat added at constant volume is not utilised for doing any external work. Assertion (A): Efficiency of a reversible engine operating between temperature limits, T, and T, is maximum. Reason (R): Efficiency of a reversible engine is greater than that of an irreversible engine. Assertion (A): Second law of thermodynamics is called the law of degradation of energy. . Reason (R) : Energy does not degrade each time it flows through a finite temperature ditterence Answers : 1, (b) 2. (c) 3. (a) 4. (a) 5. (b) aan Chapter 2 Steam and its Properties Steam is the most common working substance employed as working medium in steam hu nes, steam turbines and in atomic power plants for power generation. There occurs a change in the properties of steam during a process and that helps to attain the desired effect. Steam also finds application in process industries, and also acts as heat carrying agent in heat exchange equipment, ‘This chapter deals with the process of steam generation, properties of steam and the heating and expansion processes of vapours. The utility of Mollier chart in the solution of problems dealing with steam vapour has also been dealt with. | 2.4, PURE SUBSTANCE AND PHASE pure substance is one which corisists of only single species with characteristic feature of being sf homogeneous and invariable composition irrespective of phase or phases in which it exists pure substance can exist in three different states, e.g., water can be formed as solid (ice), liquid id gas (water vapour or steam). A system composed of liquid and vapour phases of water is also a pure substance. Even if some of the liquid is vaporised during a process, the system will still be chemically homogeneous and unchanged in chemical composition. However, it is not physically homogeneous because the liquid density is usually much greater than the vapour density. Air which is a mixture of 79% nitrogen and 21% oxygen by volume can also be treated as pure substance if its composition does not change when it undergoes a cooling/heating or expansion/compression process. However, when it is cooled and a part of it liquifies, it is no longer a pure substance. Other examples of pure substance are the vapours of Fr-12, Fr-22 and NH, ete. which are used in refrigeration and air conditioning system for producing cooling effect The characteristic features of a pure substance can be represented by the following thermodynamic diagrams p-V, p-T, T=», T-s, h~s (Mollier diagram) and p—h diagrams. The three conditions of a pure substance namely solid, liquid, vapour (or gas) are known as phases. Thus a phase is any homogeneous part of a system that is physically distinctive. It is essentially the homogeneous, chemical and physical state of aggregation of molecules comprising the substances. Each phase of a system is separated from other phases by interfaces called phase boundaries. Consider a system of an ice cube in liquid water. There are two phases, solid and liquid, and the phase boundary is the surface of ice cube. The transition from one phase to another namely melting, freezing, vaporisation/ condensation are known as changes of phases. Whenever a change of phase occurs, all the mass of substence does not change its phase simultaneously. For example, evaporation of water starts when its temperature is raised to the boiling point. However. all the water in the container is not simultaneously transformed to the gaseous phase. It remains ina mixed phase of gas and liquid, and the substance of this mixed phase is called vapour. Unlik? 94 Steam and its Properties // 95 gas, a vapour can be easily liquil - - jaws0f perfect gases do eee by applying pressure at constant temperature, The simple in charts and listed in acieee Y to vapours, hence variation between their properties are depicted 2.2, VAPORISATION, EVAPORATION AND BOILING Vaporisation refers to the process that Water vapours can be obtained by ev saporati Eoaporation is the process of vapour generation only from the surface of aliquid. The molecules having greater velocity, i.e,, kinetic energy br: i . y break away fi surrounding atmosphere. Evaporation ee yy from the liquid surface and escape to the s urs at any temy 7 i with rise in temperature of the liquid anne to a Sana involves change from the liquid phase to vapour phase. aporation and steam by boiling a baat ar reece ‘ai, it stars boiling and vapours get generated both from the free 5 © it. Boiling refers to the process of vapour formation that takes place in the whole mass of the liquid, All the liquid gets converted into vapour, when vaporisation takes place in an infinite space, ic,, in an open vessel. However, when the vessel is closed, vapours escaping from the liquid fill the free space above it and a fraction of these vapours return back into the liquid. Saturation temperature and saturation pressure : Boiling takes place at a definite temperature which depends upon physical properties of the liquid and pressure. This temperature, denoted by [,, iscalled the saturation temperature and it remains constant until all the liquid has transformed into vapour. At the saturation temperature, the boiling liquid is in equilibrium with its own vapour. The pressure at a specific temperature, at which the liquid boils or is in equilibrium with its own vapour, is called saturation pressure, At standard atmospheric pressure (p = 1.01325 bar), water boils at 100 °C. As such, at p = 1.01325 bar, the saturation temperature of water is 100 °C. Likewise, the saturation pressure at 100 °C boiling is 1.01325 bar. Quite often, the saturation pressure@s referred to as vapour pressure. 2.3. SATURATED AND SUPERHEATED STEAM Depending on its properties, a steam may be saturated or superheated. The steam is called saturated when the molecules escaping from the liquid become equal to the molecules returning to it. The saturated steam has a maximum density at a given temperature and is in thermal equilibrium with the liquid. The temperature of saturated steam (vapour) and the liquid in contact with it is called the saturation point or boiling point. The liquid at its boiling point at a specified pressure is called a saturated liquid. Such a liquid isin equilibrium with its own vapour at specified temperature/ pressure. At standard atmospheric pressure, the water boils at 100 °C and generates its own vapour. Thus corresponding to standard atmospheric pressure, the water at 100 °C is a saturated liquid. Saturated steam may be dry or wet. When the saturated vapour contains particles of liquid evenly distributed over the entire mass of vapour, it is called wet saturated steam, Wet steam is characterised by its dryness fraction which is defined as the ratio of mass of dry saturated Vapour to the total mass of the mixture. That is mass of dry saturated vapour Dryness fraction, x = Se ae es 20) m — mp+My Where m is mass of mixture, m, is mass of dry saturated steam and my (saturated liquid) in suspension with the saturated dry steam. is the mass of water vapout 96 // Basics of Mechanical Engineering The dryness fraction when expressed in percentage is called amatity of ste Wetness fraction is another term associated with wet cau noes ie eer! of water vapour or moisture in suspension with the total mass of » my my my + My ore my + My Wetness fraction, y sd priming. Thus, The wetness fraction when expressed in percentage is called priming. Thi i = jt. ality + priming = 100 percen / Saturated liquid which contains no liquid particle is called dry saturated steam. For dry saturated steam, x = 1, . Steam becomes superheated, if at a given pressure, ils temperature is higher than that of saturation temperature. The state/condition of superheated steam is Prescribed by its Preseli and temperature (,,, The temperature difference (I,,,~ f,) is known as degree of super 4 Degree of superheat = fay, ~ f, f23) where fy is the temperature of superheated steam and is the saturation temperature. Higher the degree of superheat, greater the volume occupied by steam, This implies greater distance between molecules and smaller the influence of molecular forces of attraction. At high superh the behaviour of steam becomes identical to that of ideal gases 2.4, STEAM GENERATION The process of steam generation can be divided into three stages namely (i) heating of water upto boiling point, (ii) evaporation of boiling water and its conversion into dry saturated steam (iii) transformation of dry saturated steam into superheated steam These stages have been depicted in T— 1 kg of ice at ~ 10 °C ( below freezing point by point 1. Q T-vand p ~v diagrams in Fig, 2.1. by considering t). The initial state of the substance has been denoted (1) When heat is supplied, its temperature rises to 0 (2-8). During the process of melting (phase change fr * there exists a mixed phase of ice and water * the temperature of mixed phase remains at 0 °C * there is nominal decrease in volume ; liquid water at 0 °C is hei for normal substances there is increase in volume when cha to liquid phase. °C (273 K) and thereafter, melting starts ‘om solid to liquid), avier than ice. However Be Occurs from solid phase phase from solid to liquid is called the metti sic fice, and thy d is call ing or fusion of ice, an Deny ofheat required fice into water at constant temperatit® equals 335 Kj/ kg. heric pressure of 1.01325 bar (1 atm), i (2) When the entire ice has melted (point 3) * there is only one phase, ic, liquid water at 0° * rise in temperature of water occurs with suppl Se pply of heat Point is reached, The boiling point depends upon the oon” supplied. The boiling temperature is called saturation temperature and at nor dimospheric pressure its value is 100°C The pressure cere ending to sat temperature is called saturation pressure. Thus pena ‘no At Py = 1.01325 bar, f.,, = 100 °C lat continues till boiling Pressure at which heat is be ee L— = Steam and its Properties // 97 + there is decrease in volume when temperature rises from 0 °C to 4 °C (process 3-3) and thereafter the volume increases upto the commencement of boiling (point 4) The heat required for change from liquid state to-vaporisation/ boiling point is called sensible eat 11) if 1-2 Solid state 2-3 Melting 3-4 Liquid state ° 4-5 Vaporisation 2 5-6 Vapour state 6 2 ‘Superheating & f 373| Evaporation 273p- Q 1K) For any general ° pure substance 2 6 § 373 7 B ; 2 t 277 273 7 —> Volume v Pp ' Mixture of Critical point solid and Mixture of liquid + vapour Saturated vapour line 6 — Pressure Vapour or gas —> volume Fig. 2.1. Process of steam generation 98 // Basics of Mechanical Engineering (3) When more heat is added, evaporation of water starts and ones again phase occurs. During this. phase change front state point 4 to state p , + there exists a two phase mixture of water and its vapour + the temperature remains constant til] all the water gets converte of vaporisation is thus both isobaric and isoth + there is considerable increase in volume. sto of stam at ths point called gl i i he sti At state point 5, all the water has vaporised and th S ; and are steam, The phase transformation from liquid to vapour is called vaporisation, ang the heat required for complete transformation of water fo its vapor at ora temperature called the latent heat of vaporisation. For water evaporating at 100 °C under spheric condition of 1.01325 bar, the latent heat equals 2256.9 kJ/kg. (4) Since the saturation temperature 1s a function of pressure, See can bees place along any one of the lines 4—5, 4° —5' or 4” —5", The joining of points 4—4’— gives liquid Tine and the joining of points 5—5’ —5” forms a line called the satura ted vapour line. On the let of liquid line, there exists water in the liquid phase, and on the right of saturated vapour line the water is said to exist in the superheated phase. Between state points 4 and 5 there is a mixture of steam and water, ie., wet saturated steam with varying dryness fraction. A shift in the state point A towards the vapour line makes the steam drier and drier. The saturated liquid curve is steeper compared to the dry saturated vapour line because the volume of liquid changes at much slower rate with incréase in temperature. (5) The horizontal distance between saturated liquid line and the dry saturated vapour line becomes less and less with increase of pressure and saturation temperature. The point at which this distance becomes zerois called the critical point. Critical point represents the highest temperature and pressure above which a liquid cannot exist. At the critical point, * the liquid is directly and fully converted into dry vapour without going into the phase of evaporation, ic,, latent heat is zero * the liquid and vapour are indistinguishable + the properties of saturated liquid and saturated vapour are identical. ‘The temperature and pressure at the critical point are called critical temperature t, and critical pressure p,. ; ‘ another change g 0 vapour. The proces: ermal For water, the critical values are : critial temperature 1, = 374.14 °C ; critical pressi a i zi 5 A ure p. = volume BP ere P € p, = 220.9 bar and critical volun wit ones tbe a sty and saturated state, its temperature and volume start increasiNé su] of heat. i i i " theese pe ly \e steam so ee is called superheated steam and it behav Follawing advantages occur by using superheated steam in steam power plants : y increased work capacity without having to increase its pressure ii). greater heat content of the su : iperheated steam leads to | i ae output and that results in saving in the cost of fuel, Sieemeconsumpron ors (iii) moisture content of steam leaving th i i Accordingly, the heat losses 6 the steam turbine/ engine can be kept within safe sie Ib sses due to condensation of steam are avoided to a large &%" ((2) superheating is done by utilizing the heat tof = , . uselessly to ihe inonphere 8 waste furnace gases which otherwise P* Steam and its Properties // ss 'ssed above, has been under standard atmospheric pressure Ssure, the nature of the various processes will be identical different values. In actual practice, the steam is generated atdifferent pressures below critical pre: ut the saturation temperature will have at pressure varying from 10 to 200 bar, In recent times, methods ha critical pressure of 220.9 bar. The steam so formation takes place without boiling or bubbling of water ve been developed to produce steam at pressures much above the produced at p > p,is called super pressure steam and its 2.5. SOLID—LIQUID—VAPOQUR EQUILIBRIUM Fig. 22 shows the Phase (p versus 7) diagram for water in which regions of solid, liquid and vapour are indicated. Its salient features are + 1. The single phase regions are separated from each other by saturation lines. Along the sublimation line 1-T there is - equilibrium between the solid and vapour phase, ie, the solid and vapour phases co-exist. The solid and liquid phases co-exist in equilibrium along the fusion line T—2. There is equilibrium between the liquid and vapour phase along the evaporation line T—C. Fusion line Critical point Liquid > —f---> Melting Evaporation Evaporation line Vapour Triple Point The fusion line for water has a negative slope (dp/8T <0) indicating that melting point of ice decreases with increasing pressure. However, for most substances, the slope of fusion curve is positive. Solid ——> Pressure

Temperature Fig. 2.2. Phase equilibrium diagram on P-T co-ordinates 4. The sublimation, fusion and evaporation lines meet at point T, called the triple point. The triple point may thus be defined as the point at which all the three phases - solid, liquid and vapour co-exist in equilibrium. The triple point exists at a definite pressure and temperature. For water, triple point values are tyy = 0.01 °C and p,, = 0.611 kPa 5. Sublimation refers to the heating process where solid water or ice gets directly transformed to saturated vapour phase without first melting into water. The reverse of sublimation is referred to as ablimation, -®.6. ENTHALPY CHANGES DURING FORMATION OF STEAM nt Fig. 2.1 (a) which represents formation of steam from ice at = 10°C, Since supply of dot “stage so Pressure, the heat input can be taken equal to change in enthalpy. During the process of steam formation, the enthalpy changes are as follows : () Enthalpy changes from - 10 °C to 0 °C (process 1-2) 100 // Basics of Mechanical Engineering ————__ t of ice (dit) 12 = jdt where ¢/18 the specific heal 2.09 {0 - (-10)} = 20.9 KI/ke ng, of ice at 0 °C (process 2~3) heat of fusion of ice = 335 J/kg ling /saturation temperatur, (i) Enthalpy change during melti (alt) 9-3 = latent °C to the boi (ii) Enthalpy change during heating of water from 0 °C fo 100°C (process 3-4) (ait) c., dt where ¢,, is the specific heat of water Pai we 4.186 (100 -0) = 418.6 KJ/kg (io) Enthalpy change during vaporisation at 100 °C (process 4—5) (dit) 4.5 = latent heat of vaporisation = 2256.9 kJ/kg. (2) Enthalpy change during heating of dry saturated steam upto say 250 °C. (process 5~6) (dt) 5.6 = Ss at where ¢,, is specific heat of superheated steam = 2.1 (250 -100) = 315 kJ/kg It is to be noted that enthalpy quantities are always measured from some datum. The transformation of water from 0 °C into steam involves two Kinds of changes that take place on supply of heat at constant pressure. — temperature of water changes but phase remains the same. — phase changes but temperature remains constant. ‘The corresponding heat inputs are defined as : Sensible heat (/r,) : It is the quantity of heat required to raise the temperature of 1 kg of water from 0 °C to the boiling point or saturation temperature at a given pressure. Sensible heat is denoted by letter ly, and is also called total heat (or enthalpy) of water. Sensible heat increases as the pressure increases. Latent heat of vaporisation (Ij,) : It is the quantity of heat required to convert 1 kg of water at saturation temperature for a given pressure into dry and saturated steam at thal temperature and pressure. The value of latent heat is not constant, it decreases as the pressure increases and becomes zero when the critical pressure is reached. Depending upon the condition of steam, the heat or enthalpy values are defined as : () Total heat of wet steam : It represents the quantity of heat required to convert 1 kg ¢f Water at 0°C into wet steam at constant pressure Iggy = y+ X Ng (24) where x is the dryness fraction of wet steam. The sensible heat increases with pressure. ii) Tot : it (i) To fat heat of dry saturated steam :Tt represents the quantity of heat required to convert 8 of water at 0°C into dry saturated steam at constant pressure hh = ligt hg = hy The enthalpy of dry saturated steam increases with pressure, 5) -F 104 Steam and its Proper ) Total neat of superheated steam : It represents the quantity of heat required to convert 1 kg of water at 0°C into superheated steam at constant pressure Thay = ligt Ig + o,, (b (26) value of specific heat of. ia The value of specific heat of steam at constant pressure, depends upoa the degree of superheat and the pressure of steam generation, Its average value is taken from 2.0 to 2.1 kI/ke, 2.7. VOLUME OF DRY, WET AND SUPERHEATED STEAM The specific volume of a fluid is the volume occupied by a unit mass of the fluid. For dry saturated steam, it is denoted by the letter v,. Its value decreases with increase in pressure, and the values corresponding to different pressures are listed in steam tables. sup 4) Wet steam : The volume of 1 kg of wet steam equals the volume of dry portion of stzam plus the volume of water in suspension. If x is the dryness fraction of wet steam, then 1 kg of wet steam consists x kg of dry steam and (1 - x) kg of water in suspension. Thus the volume of wet steam is Vp = XV, + (1 - x) (2.7) where vyis the specific volume of water and v, is the specific volume of dry saturated steam. By re-arrangement, x = When x > 0.8 and p < 30 bar, the specific volume of water is practically insignificant and can be neglected. Accordingly, Pw Uy = xy and x= y (2.8) Superheated steam : The superheated steam behaves like a perfect gas and, therefore, its volume can be worked out by applying Charles law to steam at the beginning and at the end of superheating process. Thus (2.9) np where v, and T, are respectively the specific volume and absolute temperature of dry saturated Seam ang ANd Tay Fe respectively the specific volume and absolute temperature of superheated steam, 2.8. EXTERNAL WORK AND INTERNAL LATENT HEAT When water evaporates to form steam, its volume increases from v, to v, at constant »-ressure. The work is thus done by steam in increasing its volume. This work is called external work of evaporation. External work = p (2, - %) At low pressures, specific volume of water vis. extremely small compared to ¢ neglected. Then External work = p dg In case of wet steam with dryness fraction x, the volume of steam would be: and hence e210) and accordingly amy External work = p x 0 102 // Basics of Mechanical Engineering A certain amount of latent heat supplied to water during the evaporation process! Utilized in expanding the volume and thus producing external work. The latent heat of steam minus th external work is called the internal latent heat. Internal latent heat = Iyg ~ p 2 (212) 2.9. INTERNAL ENERGY OF STEAM The actual heat energy above the freezing point of water stored in energy of steam. The work of evaporation is utilized in doing stored in the steam, Accordingly, internal energy of steam can the steam is known as interngy external work ‘and is thus no, be determined by subtracting work of evaporation from the total heat/enthalpy of steam. That is : w= Nt - po For wet steam : w= (yt x hg) ~ pxey For dry saturated steam: — u = (lip + lig) ~ Pg For superheated steam = ligt liyg + Cys (toup ~£9) ~ P Psup +-(2.13) 2.10. ENTROPY OF STEAM The heating and evaporation of water during the steam formation process takes place at constant pressure. Even superheating of steam is done at constant pressure. The entropy of steam can, therefore, be calculated by using the relations for entropy change at constant pressure. Entropy of water (s,) : Let one kg of water be heated from temperature T, to T, at constant pressure. Entropy change is then given by 8Q aT = =o, . T cays Upon integration from initial state 1 to final state 2, ds T a= Gee If 0°C is taken as datum : s, = 0 and T, = 273 K. That gives 5 = log, f= Be o73 where s,is the entropy of water at any temperature T above freezing point of water. If heating of water continues upto saturation temperature Ts, then log, J 5, = G log. ws 14) Entropy of evaporation (s,) : Evaporation of water takes place at constant pressure and constant temperature T,. The quantity of heat supplied during evaporation equals x Ii. if the steam is wet at the end of heat supply, and equals hg if the steam is dry saturated at the end of heat supply. Thus change of entropy during evapofation . = 7 for dry atid saturated steam xh ia . 7 for wet saturated steam with dryness fraction ¥ ww ee Steam and its Properties // 103 Thus entropy of wet steam reckoned above the freezing point of water (0 °C) is given by wer ~ entropy of water + entropy change during evaporation xh Be TE Tt eh = 5+ x (5,-8) Likewise, the entropy of dry saturated steam (i, x = 1) (2.15) reckoned above 0 °C works out i Sdry = 5p “5+ 6 S)=5 (2.16) Entropy of superheated steam : Entropy change during superheating, which takes place at constant pressure, is given by heat of superheat _ 89 aT ds = SE superheat _ dy _, aT T T BT If T,,» is the temperature of superheated steam, and T, is the saturation temperature at the considered pressure, then T, hp ps 108. rT ds = Thus the total entropy of superheated steam reckoned above the freezing point of water 0°C)is Toy Seup = 57+ Spy + Cys log, fa 2217) ‘The specific heat of superheated steam, c,,, varies from 2.0 to 2.3 kJ/kg K depending upon degree of superheat and superheating pressure. ~ 2.11, STEAM TABLES ‘Thesimple laws of perfect gases donot apply to vapours, hence variations between their properties are depicted on charts and tables. The preparation of steam tables has been made possible by studying experimentally the various properties of steam at different conditions of steam formation. The experimental data was then utilized to formulate suitable equations of state in different regions, and subsequently obtain comprehensive data on steam properties. The steam tables give values of specific volume, enthalpy and entropy for saturated liquid and dry saturated vapour tabulated against pressure (p) or corresponding saturation temperature (I,). A typical structure of such ‘ables is given in Table 2.1. Such tables make it possible to rapidly find the basic characteristics of steam according to the en parameters. The method of interpolation is used to find the parameters for intermediate ‘Wes of pressure and temperature (not given in tables). ____ The properties of superheated steam are tabulated separately. The values of specific volume, Snthalpy and entropy not only depend on pressure but also on temperature or degree of superheat. A typical structure of such tables is given below. . sive val = — Table 7.1. 1, Properties of Dry Saturated steam Absolute | Saturation ] Specific Volume Specific enthalpy Specific entropy Pressure, bar | temperature m3/kg kJ/kg Kj/kg K P t % 2, hy hy h, s Se 5 10 1799 | 0.001127 | 0194 762.6 | 2013.6 | 27762 | 21382 | aas4e | 6.5825 30 2838 | 0.001216 | 0.0666 | 10084 | 17939 | 28023 | 26455 | 35382 | 6asa7 2. Properties of Dry Saturated steam Temperature | Absolute | Specific Volume Specific enthalpy Specific entropy °C pressure m/kg Ki/kg Wi/kgK bar t, P % ¥, hy Ig hy 5 al 10 0.0123 | 0.001004] 106.4 420 | 24777 | 25197 | 0151 | 8750 | soo 50 0.1235 | 0.0c1012 | 1203 | 2093 | 23827 | 25827 | aos | 7372 | sor Buaaulbug jes1ueysayy Jo solseg // POL | operties // 105 =o Steam aan ive Table 2.2, Properties of Superheated Steam FR = —— 7 fe a > as 250 300 350 | 400 2 8) jz a 0.474 05s | 0570 | O6i7 | @ . B.A 2960.7 3064 3167.7 3271.9 | § 7.059 7271 7A6 7.633 | 779% | e |G mae 0.152 0.169 o1s7 | 0.203 | (198.3) 4 2796.8 2923.3 3037.6 314.75 3255.8 | * S25 6.709 6.918 7.102 7.269 | The first horizontal line gives the tem column gives the absolute pressure in bi tothat pressure. The perature of steam in degrees celcius and the first vertical s ars alongwith the saturation temperture corresponding second, third and fourth horizontal lines show the specific volume, enthalpy and entropy of superheated steam arranged in increasing order of magnitude. EXAMPLE 2.1 Calculate the dryness fraction of steam which has 1.25 kg of water in suspension with 40 kg of steam. Solution : m, = 40 kg and m,,= 1.25 kg m, 40 tm, = 40+ 1.25 7 0.9696 = 0.97 Dryness fraction, x EXAMPLE 2.2 Using steam tables, determine the mean specific heat for superheated steam at 1 bar and between 150°C and 200°C. Solution : From steam tables of superheated steam and at 1 bar pressure, we have At 150°C: Igy, = 2776.4 KI/kg At200°C: Heyy = 2875.3 KJ/kg 2875.3 = 2776.4 + c,, (200 - 150) 75.3 — 5 oa Bie = 1978 ki/kg K EXAMPLE 2.3 Determine the state of steam, i.e., whether is wet, dry or superheated in the following cases (i) Steam has a pressure of 10 bar and specific volume 0.175 m’/kg. ii) Steam has a pressure of 15 bar and a temperature of 220 °C. (iii) Steam has a pressure of 20 bar and if 2700 kJ/kg of heat is required to generate the steam from water at 0 °C. Solution : (i) From steam tables, specific volume of dry saturated steam at 10 bar is v, = 0.194 m°/kg Since the specific volume of the steam whose quality is to be determined is less than the specific Volume of dry saturated steam, the steam is wet and its dryness fraction is given by specific volume of given steam at 10 bar Dryness fraction, x = “ral energy and entropy of superheated steam al ressure and 220 °C. The volume of water may be neglected and take specific heat of superheat equal to 2.2 Ki/kg K, golution : Corresponding to 15 bar Pressure, the following values can be read from the steam tables + Uy = 0.132 m3/kg ; hyp= 844.7 Kj/kg ; Ng = 1945.2 KI/ kg, ; 5, = 2.314 kJ/kg K ; Sg = 41261 ki/kg K and beg = 198.3 °C (0 Total heat of 1 kg of superheated steam ig Mayy = hy eg + Cy, (sup ~ at) ~ 844.7 + 1945.2 + 2.2 (220 - 198.3) =2837.64 kykg (i) The superheated steam behaves like a perfect Bas and as such cout by applying Charles’ law, ie, T, uy xe sup = 1: . 220 +273 5 © 0132 * 396-3 4 975 = 0.1381 m/kg (ii) External work = pv = 15 x 108 x 0.1381 = 207150 J = 207.15 kj Internal energy, u = h ,,, ~ external work = 2837.64 - 207.15 = 2630.49 kj/kg (iv) The entropy of superheated steam is log, Sup = 8 5+ ops 1080 2204273 = log, 04223 2.314. + 4.1261 + 2.2 log, 798.34373 7 6539 Ki/kg K EXAMPLE 2.12 Steam at 10 bar and 200 °C is cooled till it becomes dry saturated and is then throttled to 1 bar Pressure. Determine the change in enthalpy and heat transferred during each process. Also find the quality of steam at the end of throttling process. Take c,, = 2.25 kJ/kg K for superheated steam, 10 bar 4 10 bar Solution : 200°C ry saturated ae cooling throttling Fig. 2.3. At 10 bar and 200 °C (steam is superheated) y= Iayyq = 2827.9 KJ/kg At 10 bar and dry saturated, hy = lig + ly = 762.6 + 2013.6 = 2776.2 kI/kg, * Change in enthalpy during cooling, = hy ~ hy = 2827.9 - 2776.2 = 51.7 kI/kg OS 4 1110 // Basics of Mechanical Engineering 4 (ii) Throttling is a constant enthalpy process, i.e., Ah = 0 during process 23. Therefore, ¢ the throttling process, we can write hy = hy Atl bar: hg 417.5 kJ/kg and lijs = 2257.9 kJ/kg, 2776.2 = hg + Iigg + Spe At = 417.5 + 2257.9 + 2.25 At 2776.2 - 417.5 — 2257.9 _ ° -. Degree of superheat At = 555 44.8 °C EXAMPLE 2.13 — Steam from a boiler is delivered at an absolute pressure of 15 bar and dryness fraction of 0.¢5 into a steam supetheater in which the steam receives additional heat at constant pressure ang its temperature increases upto 300 °C, Determine the amount of heat added and the change in internal energy for unit mass of steam. Solution : For the initial state of steam at p = 15 bar and x = 0.95, we have from steam tables ny = tpn +1 Iga = 844.7 + 0.95 x 1945.2 = 2692.64 kJ/kg, Dy = % Vg = 0.95 * 0.132 = 0.1254 m3/kg y= hy PP 5x10! = 2692.64 - eee = 2504.54 kJ/kg The enthalpy and the specific volume of steam in the final state are found from tables for superheated steam (p = 15 bar and ¢ = 300 °C) hy = 3037.6 kJ/kg and v, = 0.169 m3/kg, 15 x10° x 0.169 Td = 2784.1 kJ/kg 3037.6 Uy = hy - po. +. Quantity of heat supplied in the superheater is 4 = hy ~ hy = 3037.6 ~ 2692.64 = 344.96 kj/kg, and change in internal energy is du = ty ~ u, = 2784.1 ~ 2504.54 = 279.56 ki/kg, EXAMPLE 2.14 Steam is supplied from the boiler at a pressure of 16 bar and 98 percent dry to a steam engin’ As the steam flows through the pipeline, its pressure remains constant but it loses 25 KVM of heat due to poor pipe insulation. What would be the condition (temperature and drynt* fraction) of steam at the engine end of pipe line ? Solution : Let suffix 1 and 2 refer to the state of steam at the boiler end and at the engine & of the pipe line. From steam tables at pressure 16 bar : f, = 201.4 °C Nig. = Mp = 858.6 KI/KR 5 gy = Igy = 1993.2 KJ/kg hy = fy + Iga = 858.6 + 0.98 x 1933.2 = 2753.14, kI/kg Mtg = Higa + 2 hygg = 858.6 + xy * 1933.2 Steam and its Properties // 144 According (0 the given condition : ji, ~ 25 = Ny 2753.14 - 25 = 858.6 + 1933.2 x, — 2753.14 ~25 ~ 858.6 = Ee 3 ~ 858.6 2 1933.2 eae Thus the steam is 0.967 dry and has a temperature of 201.4 EXAMPLE 2.15 Aclosed metallic boiler drum of 0.25 m’ capacity holds steam at 10 bar pressure and 195°C. Determine the quantity of steam in the drum. (b) At what pressure in the drum the si cooled? (c) What would be the pressure and condition of steam in the drum if the cooling continues till the temperature of steam becomes 120.2°C ? Solution : The saturation temperature corresponding to 10 bar pressure is 179.9°C. The given steam has a temperature of 195°C which is higher than the saturation temperature. Therefore the given steam is superheated and its volume is given by Psy Teup _ 0.194 x (195 +273) _ a7 aT (179.9 + 273) volume of boiler drum specific volume of steam 0.25 °C at the engine end. team would become dry saturated if the drum is mm Mass of water = mass of steam = 25 kg 0.2 (b) At V_ = Vg, = 0.2 m’, the saturation pressure is 9.7 bar (0) After subsequent cooling the temperature becomes 120.2°C. At this temperature, saturation pressure = 2 bar specific volume of dry saturated steam = 0.885m°/kg Then ; 0.2=x% 0885; x= 0.225 Thus, when cooled to 120°C, the steam will be at 2 bar pressure and 0.225 dryness fraction. Heating and Expansion of Vapours Constant volume process: Consider unit mass of steam undergoing constant volume heating Process from initial wet state 1 (pressure p, and dryness fraction %,) to the final superheated State 2 (pressure P2 and temperature Tyupo) P. T Closed rigid 2 vessel Heat input v 5 4112 // Basics of Mechanical Engineering 4 dysy (i) Work done w, ve -ocess. Obvious the work done is zero in a constant volume Pr (ii) Applying the first law of thermodynamics ala 8q = Sw + du = uy - My + buey The enthalpy lt and internal energy are correl Quen = (lt, ~ Pav2)— (Ih ~ Pata) The enthalpy values at the end states are hy = Ny, +1 ftg, and hy = Nig, +p (Teupa —Teatt) “The heating or cooling of steam in a closed rigid vessel represents a constant volume proces EXAMPLE 2.16 © ——————————$—$____{$_$_$_$_ Steam at 10 bar pressure and 0.9 dryness fraction is cooled at constant volume at 160 °C. Why lated as h = u + pv. Then, will be its final condition ? Solution : Initial volume v, = (= x) By + Uy (1-22) Bf) + & Up volume remains constant, », = v2, and therefore, (La) Up #4 Ug, = CL ~ 2) Op * yO Neglecting specific volume of water, we may write, Final volume v, Sine X1 Up From steam tables : at 10 bar, 0 “0.9 x 0.194 X Ugo 2% 0.194 m3/kg and at 160 °C , v4 = 0.306 m?/kg xy * 0.306 0.9 0,194 0.306 EXAMPLE 2.17 -ssa SSS ee A pressure cooker contains 2 kg of steam at 5 bar pressure and 0.9 dryness fraction. Find tht quantity of steam which must be transferred so as the quality of steam becomes 60% dry. Al calculate the pressure and temperature of the steam that exists in the cooker after the he rejection, Solution: From steam tables corresponding to 5 bar pressure = 3, . ° ; 2, = 0.375 m?/kg ; It, = 640.1 kJ/kg and Ing = 2107.4 kJ/kg, Specific internal energy at the initial state 1, my = hy pyr = Opa + Mea) ~ Prt Oy = 0.5706 or 57.06% = (6401 +09 x 1074) - 520°(09x0.975) 10 = 2536.76 - 168.75 = 2368.01 KI/kg rties / 193 Steam a its Prop As the volume remains constant during the cooling process : Per = XpV_9 go = Ao, = 98 0.375 = 0.5625 m3/kg, ea) 0.6 . B The corresponding steam Properties as read from the steam tables are : P2 = 3.25 bar; ty = 136.25°C hy = 573.2 K)/kg ; hygy = 2155.1 kJ/kg Now : up = Itpy + x2 Ngo ~ Po Xp gp = (673.2 + 0.6 x 2155.1) - 2:25%210" x (0.6 x 0.5625) a pues) = 1866.25 - 109.68 = 1756.57 kJ/kg Heat to be transferred Q = du =u, - uy = 1756.57 ~ 2368.01 = - 611.44 J/kg Total heat transferred = 2 x (— 611.44) = - 1222.88 kj The - ve sign implies that heat is rejected from the system. The steam remaining in the pressure cooker after rejection of heat is at : pressure = 3.25 bar and temperature = 136°25 C EXAMPLE 2.18 Arigid tank of 1 m? volume contains dry saturated steam at 0.2 MPa. Due to poor insulation, there is heat transfer to the surroundings and the pressure drops to 0.1 MPa after some time. Make calculations for the final condition of the steam and the amount of heat transferred. Solution : At 0.2 MPa (2 bar) 0 = Y,1 = 0.885 m?/kg ve 1 1” 0.885 At 0.1 MPa (1 bar) v2 = (1 ~ x2) Up + Xp Ugp = X:Vyp = 1.694 xy Since the tank is rigid, the volume remains constant (v, = v,) and therefore, 1.694 x, = 0.885; x, = 0.522 7 was the final condition of steam corresponds to wet steam of dryness fraction 0.522 at a (i), = hg, (dry steam at 0.2 MPa) = 2706.3 kJ/kg hy = Ng + Xz Ngo (wet steam at 0.1 MPa) = 417.5 + 0.522 x 2257.9 = 1596.12 kJ/kg For a constant volume process work done is zero and therefore, from principle of energy Conservation Mass of steam m = = 113 kg 2 = du = (ug ~ uy) = (hy = Poa) ~ (hy ~ PyPs) = (tp - In) - 1 2 - Pv) 0.885 (0.1 - 0.2) x 108 = (1596.12 - 2706.3) - { 0 = - 1021.68 kJ/kg gineering ——— 414 11 Basics of Mechanical En — red as neat 10 te surroundings «Total energy transfer = mh? : 13 * (2021-68) = = 11585 ng ofsteam undergone 288 Os fraction *1) © the fina constant pressure heat, 1 | superheat nit M Constant Pressure Proc myn process from initial wet state (pressures Pap temperature Topo)? Pa : 2 2 (pressure p and P ‘ess: Consider sssure, Py v Heat input Fig. 2.5- ‘The specific volumes and specific enthalpies at the initial and final states can be found frox the steam tables. aM 7 ny = + Mt er 1 = U2 OOF On = OP Tata 2 (i) Work done 1).2 = fi (Taupo * Tet2) hy = hg, +p paVv= ple, - %) are correlated as h = u +P? Then (lig =I) - P22 PA”) iy ~ hy) - Pr ~ %1) (ii) Applying the first law of thermodynamics By = but du; 2 =P2-%) * (hy = (ty - fy) nstant pressure is equal to changes in enthalpy. ant pressure heating process: 1 {i The enthalpy ft and internal enerBy Change in internal energy (H ~ %) = = hy) - pz - 2) Apparently the heat transfer at co ‘The generation of steam in a boiler represents a const EXAMPLE 2.19 aa accep ly contains one kg of wet steam of quality 0.8 at 0.1 Ml akes place at constant pre’ i ‘ ii Make calculations for the work done and Terenas temperature of stam #36510 Solution : For a constant pressure process ,_ » = tt iin For steam tables at 0.1 MPa (1 bar) aie 2, _ Eners! (Pa. Rd 4 - (Lom) eat a M1 =m My = 0.8 x 1.694 = 1.3552 m*/kg Vsyp (1 bar and 350 °C) ; by interpol 552 m*/kg 2.639 43.103 polation = 2.871 m3/k; Worl 4 fork done w,_) = 0.1 x 108 (2.871 - 1.3552) = 151580 J = 151.58 kJ/kg yr _—— Steam and its Properties // 115 (i Again from steam tables at 0.1 MPa (1 bar) hy = hy + x, Ne 74175 + 0.8 x 2257.9 = 2923.82 kj/kg 2 =Msyp (1 bar and 356 °C) ~ 3074.3 + 3278.2 TS = 3176.25 1 /kg For a constant pressure process the heat interaction e Heat interaction = (h, - hy) h, quals the change in enthalpy = 3176.25 ~ 2223.82 = 952.43 ki/kg EXAMPLE 2.20 Wet steam at 20 bar pressure and 0.9 dryness fraction is heated reversibly at constant pressure toa temperature of 300 °C. Make calc: ulations for the work done, heat supplied and changes in internal energy and entropy. Rep: resent the process on T—s diagram and indicate there upon the area which represents the heat interaction. Solution : Refer to Fig 2.6. For a constant pressure process, Wy2 =P @)- %) From steam tables at 20 bar 21 = (L~) on +x, Og = By = 0.9 * 0.0995 = 0.08955 m3/kg, V2 = yy» (20 bar and 300 °C) 2p =20bar Heat suppliod ‘Temperature —> = 0.125 m3/kg ! + Work done w,_, = 2 * 105 (0.125 - 0.08955) " entropy ——» = 70900 J/kg = 70.9 kJ Fig. 2.6. Again from steam tables at 20 bar, 4, 4 tn +8 Men = 907 + 0.9 x 1693 = 2430.7 kJ/kg My = Wgyy (20 bar and 300 °C) = 2772.6 kJ/kg “ Change in internal energy du = (up~ 1,) = 2772.6 - 2430.7 = 341.3 ki/kg From the principle of energy conservation, 2 = Wy + du = 70.9 + 341.3 = 412.2 kifkg Altematively : For a constant pressure process, the heat interaction equals the change in enthalpy. hy Ng +X Igy * caf 108.6 + 0.9 x 1888.6 = 2608.34 kJ/kg j hy = Itayy (20 bar and 300 °C) = 3023.5 kJ/kg *: Heat interaction = hy - hy = 3023.5 - 2608.34 = 415.16 kJ/kg 416 || Basics of Mechanical ‘Again from steam t 1 ables at () bars +x, Sit N70! 25,948 K)/ke °C) = 6.766 kJ/ kB K 20 bar and 300 _ 0.818 Ki/k6 & 5q = Soup |. Entropy change 82 ~ 51> 66 - 5.998 = ene steam undergoing Leven from initial superheated state 1 (pressure p, and te . ction %) “ sion process adiabatic expan: fe 2 (pressure I’2 to final wet stat ( During isentropic process, entropy remains constant. Thus, Tour 5, = 5) Sa + cp lopez Sh +225 fen sat - I, sy, +Cploge p lOBe Sf “n reais ” fis (i) Change in internal energy, hs reeDA 7 ty = My = (ty ~ Pa2) ~ (i - Pr?) where 0; = %_, % = 1a ey Mae and B= 2M, h ) and hy My, +2 eat y= Ia, pCtags Ten ‘or a re i i smal wersible adiabatic process, no heat ad. ded to or subtracted from the * 4270 Then from first law of thermodynami eee ce 2 = (Ny = py?) ~ (ly - ppp) cen ee asl # Dry saturated steam ini i 1m initiall cylinder fitted with a fri ly at a pressu af ressure of 60 ; expands to a pressure fricionless piton, As th 0 kPa is contained | kPa. Calculate the wi pion moves aieah a thermally # ark done by s y outwards, # y steam. Solution : At i state point?: —p, = 600 kPa (6 by ar) and ri 700 en an wate : 1 = Sy 6,761 k| oK 1 point 2: py = 60 kPa (0.6 ing Roms ap © Mm and its Pi sf 497 129 kj /ke, = 1.145 kJ/kg K and 5), = 6.386 kJ/kg K 2 8 5, = 6.386 kj/ kg K since the cylinder is perfectly insulated, te te and therefore, 60 kJ/kg 5 Wye there is no heat interaction, iv., the process is adial Sp 46.761 = 1.145 + x, x 6,386 6.761 ~1.145, 6.386 and ty = up + xy oi = 0.879 4 2 = 360 + 0.879 x 2129 = 2231.39 kJ/kg, From the non-flow energy equation ha = M2 (ly - 4) 0 = wy.» + (2231.39 - 2568) +: Work done w, = 2568 - 2231.39 = 336.61 ki/kg, . Constant temperature (isothermal) process: Consider unit mass of steam undergoing heat addition at constant temperature from initial wet state 1 (pressure p, and dryness fraction x,) to final superheated state 2 (pressure p, and temperature Tuya) . Fig. 2.8. For an isothermal process, the temperature and pressure remain constant in the wet region, ie, p, =p, and T, = T,. Once the steam is in superheated region, it behaves like a perfect gas and obeys the gas laws. Apparently then the expansion process - 2 in superheated region is hyperbolic, ie, py, = py dy The entire process 1-2 can be analysed in two parts : (i Process 1-a: Heating of wet steam at a constant temperature till it becomes dry saturated. s is similar to heating at constant pressure and accordingly Wy-g = Pq ~ 2) where p; =p, =P = (hy ~ Fy) ~ Pa ~ %) Gra =H ~ By . (ii) Process a-2: Heating of steam at constant temperature in the superheated region is hyperbolic, “2, it follows the Boyle’s law pv = constant. For that e : = Pata Pag = Po Vsup2 f 0 Po Then the temperature Tuy can be-worked out by applying Charle's law. That ts a Tr Ty 418 // Basics of Mechanical Engineering where T, = saturation temperature corresponding to pressure p, ( p,) and 0, = specific volume of dry saturated steam at pressure p, Polytropic process (po" = constant): Consider unit mass of steam undergoind polytrop;, process from initial state 1 (pressure p,, dryness fraction x,) to final state (pressure p,, drynes, fraction x,). Then Prey Poy"; Pr(% Vg)" = Pr (Fa ep,)" \ ata (ar Us, | P2 Depending on the value of x, the steam at its final state would be wet (if x» <1); dry saturate (if x, = 1) and superheated (if x, > 1) ; The volume and temperature of the superheated steam can be determined as follows : ny" Put)" = pa(Oaga)” 5 ay = 31%, () FE P2 Usup2 v; Veup2 . roe Tyg = Tet. Tsp ~ Tear ‘sep? 2, ‘a where T.,. is the saturation temperature corresponding to pressure Pz ()) Work done w,_, = PLP = P2t2 m1 (ii) Change in internal energy du =u, ~ u, = (Ita ~ Py.) - (hy - p24) (iii) Heat absorbed or heat transferred M2 = Wy2 + du = wy_5 + (uy ~ uy) The enthalpy values are read from the steam values corresponding to the initial and final conditions of steam, That is Iho My +t hg, and hy = hy tx hp, = hy +hp, for sry saturated state = lp, + tg, + ¢p Tsao ~ Toya) for superheated state EXAMPLE 2.22 for wet state Steam at 10 bar and 250°C expands polytro b 0 Pically to a pressure of 1 bar. If tn for the polytropic process is 1.2, calculate (i) specific volume and tem; ante fe Sansa (a heat interaction, and (iif) change in entropy, aad Solution : At 10 bar and 250 °C (steam is superheated) 2 = 0.2328 m3/kg ju, = 2711 Ki/kg hy = 2944 \J/kg and 926 kI/kg K AS PrP" = P20" 5 02 = 0, (py/py)V/n a V2 = 0.2328 x (10) 1/12 = At 1 bar (state point 2) », 694 m3/kg & 17 ISG i Wp = 2089 KI/kg = 1 1.586 mike / "a Np = 417 Ki/kg ; 258 KI ky , Sp = 1.303 ite and Spa = 6.056 kJ/kg, ince ®> < Y%2_ the steam is wet with dryness fraction 2, _ 1.586 1.694 7 0.936 x)= Pen ‘The temperature after expansion will be the saturation te 99.6 °C mperature corresponding ies 3 My “Up +X Wa = 417 + 0.936 x 2089 = 23728 kI/ke hy = hip * x2 Ngo = 417 + 0.936 x 2258 = 2530.5 kJ/kg 82 = Sp + Xp Seo = 1.303 + 0.936 x 6.056 = 6.971 kJ/kg Pi = P20» done w,_5 = Work done w,. = PL=P = 10x 10° x 0.2328 - 1x 10° x 1.586 oS ae = 371000 J = 371 kJ From principle of energy conservation, Heat interaction = q)_9 = (uy ~ 1) + w,_> = (2372.8 - 2711) + 371 = 32.8 ki/kg, Entropy change = s, ~ s, = 6.971 - 6.926 = 0.045 kJ/kg K EXAMPLE 2.23 Wet steam at 1.5 bar and 9.8 dry occupies a volume of 0.05 m? ina cylinder where compression takes place so that pv = constant (that is hyperbolically) until the volume has fallen to one- fifth of the original volume. Determine the work and heat transfers and the final condition of steam, Solution : Specific volume of dry saturated steam at 1.5 bar = 1.159 m3/kg Mass of steam, m = 7359 3<0,8 = 0.0539 kg Vy _ 0.05 Final volume, V, = oh 7001 m? VY Final pressure, p= Pi (] =15%5=7.5 bar A If x, is the dryness fraction of steam after compression to 7.5 bar, then 27 Taxa ~ 0.0530x 0.2565 ~ 0728 where 0) = Saree (by interpolation) 0.2565 is the specific volume of dry saturated steam at 7.5 bar My yt et = 467 + 0.8 x 2052 = 2108.6 KI/ky Hy = Mp + Xp Mhgo = BOAT 723( _ 1687) = 2057.8 kI/kg + Total change in internal energy m (Wy = 4) = 0.0539 (2057.8 - 2108.6) Work done during compression ~ 2.738 kJ (decrease) y seas toe 2 =p, Vy Bey = 1.5 * 10° « 0.05 log, = - 12070.8 J = - 12.07 kJ The negative sign implies that work was done on the system From non-flow energy equation, 8Q = ow+du = -12.07 + (- 2.738) = - 14.81 kJ The negative sign implies that heat will flow from steam to walls of cylinder. 2.12. TEMPERATURE-ENTROPY (T-s) AND ENTHALPY-ENTROPY (h-s) DIAGRAMS The solutions to problems dealing with steam vapour as working substance are easily and rapid) obtained by referring to charts/diagrams which have been Prepared by having the data fre steam tables. The salient features of two such plots which are of considerable importance = mentioned below : (a) Temperature-entropy (I-s) diagram: () The absolute temperature is plotted on the axis of ordinate and entropy on the abscis (i) The liquid boundary line originates at the axis of ordinates at a temperature of 273164 this has to be so because entropy of liquid at the triple point is equal to zero. (ii) The boundary curves (liquid line ABCDE) and the saturated vapour line (EFGHI) di the diagram into three parts ; to the left of AE is the liquid region, between the line! ; and Elis the wet vapour region, and to the Tight of line E1 is the region of superheated St" (2) The boundary curves meet at point E which is the critical point of water with prose 221.2 bar and temperature 647.31 K, (v) The constant pressure lines are parallel to the constant temperature lines in the wet 2 ., These lines become curved in the superheated region, oO re een or constant ene fraction and constant volume ie ee (ei) Theslopesof constant pressurelineinfhelinnah oer ea nes the superested ty the tata She liquid, wet and superheated region are gev ar (z)- Steam and its Propert 121 (Critical point 647.31 K E Temperature Isothermal 0.00611 bar 273.16 K s Entropy Fig. 2.9. Temperature-Entropy Diagram (ix) The area confined between the line of a reversible process and the abscissa represents the quantity of heat added to 1 kg of working medium, and is equal to q = fras. (2) An isothermal process plots as horizontal line and a reversible represented by a vertical line. The temperature-entropy diagram permits observation of change in the temperature of working medium and makes it possible to find the quantity of heat involved in the process. Accordingly itis put to an extensive use in the investi igation of thermodynamic processes and cycles, (6) Enthalpy-entropy (h—s) diagram : Steam generation is done at constant pressure and for constant pressure heating 5q = dit. Thus calculations for heat supplied can be done readily if enthalpy-entropy diargam is drawn tather than. temperature-entropy diagram. In the enthalpy-entropy (ht — diagram, enthalpy is laid along the axis of ordinate and entropy along the axis of abscissa. Such a diagram was suggested. by Mollier in 1904 and it is usually referred to as the Mollier diagram, The following observations (in be made from Fig. 2.10 which shows the general characteristics of h — s diagram showing Water line and saturation line as one-curve : adiabatic process is (The diagram can be divided into three regions. Below boundary curves 1—A~2 is the tegion of wet saturated steam. The region of superheated steam lies above the “per boundary curve A—2, and that of liquid is to the left of lower boundary curve 1—A. Bez ds A are and have converging tendency towards origin. In this region, the constant tempera lines coincide with the constant pressure lines. dh (ii) Constant pressure lines are straight in the wet region as their slope is equal to 7 122 // Basics of Mechanical Engineering oe Region of superheated steam Enthaipy Upper boundary curve Lower boundary curve Region of wet steam Constant quality lines os Entropy Fig. 2.10. Enthalpy-Entropy Diagram (Mollier Chart) (ti). In the region of superheated steam, the isobaric and isothermal lines diverge; the isobar lines have a positive slope and turn upwards, and the constant temperature lines tend towards a horizontal straight line. This may be attributed to the fact that at high temperatures the behaviour of superheated steam approaches that of an ideal gas : I= f (7) alone. (iv) Lines of constant dryness fraction, shown in the wet region, issue from point A. They a? approximately parallel to the saturation line which corresponds to quality equal to unit’ (v) Anetwork of constant volume lines may also be plotted ; these isochors rise more steep! upwards compared with the isobars. (i) The throttling process, which is a constant enthalpy process, appears as a horizontal lin A reversible adiabatic process plots as a vertical line. The saturated liquid region is not required for solving engineering problems. This makes Possible to make the working part of the diagram on a larger scale {or greater convenien® Accordingly, in the commercial Mollier charts, the water line is dispensed with and only the d" the usual constant temperature, constant press and constant quality lines, The throttling process has been shown represented by line 1-2 and the isentropic process by line a~b~c. The Mollier chart is a useful t turbin 3 ant such as no. with an ae ‘ol in the analysis of steady flow device: 'es. The chart makes it possible to Tapidly determine the steam paramet ee sufficient for practical purposes and toa change in the state of steam, h am and its Properties / 183 Sives solution to many thermodynamic pre Constant temperature lines Dry saturated line Constant ° pressure lines . Constant quality lines Entropy Fig. 2.11. Commercial Mollier chart EXAMPLE 2.24 Represent the following processes on h—s co-ordinates and use the Mollier diagram for obtaining solution to these processes for the mentioned conditions : (a) Steam initially dry and saturated at 15 bar is throttled to a pressure of 1.5 bar. What is the final condition of steam and the entropy change during the process ? | ©) Steam initially at 0.95 dry and 12 bar expands isentropically in a non-flow process to a final dryness fraction of 0.8. What is the final pressure of steam and enthalpy change during the process ? Solution : Refer Fig. 2.12. (®) ( Locate the state point 1 which is the point of intersection of constant pressure line 15 bar and the dry saturated line. (i) Enthalpy remains constant during throttling and as such the throttling Process is represented by a horizontal straight line. Draw a horizontal straight line from Point 1 until it meets the constant __ Pressure line 1.5 bar at point 2. (ii) Drop perpendiculars from the initial and final state points on the axis of abscissa.

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