Thermodynamics: An Engineering Approach
Thermodynamics: An Engineering Approach
9th Edition
ISBN: 9781259822674
Author: Yunus A. Cengel Dr., Michael A. Boles
Publisher: McGraw-Hill Education
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Chapter 14.7, Problem 88P

Atmospheric air at 1 atm, 32°C, and 95 percent relative humidity is cooled to 24°C and 60 percent relative humidity. A simple ideal vapor-compression refrigeration system using refrigerant-134a as the working fluid is used to provide the cooling required. It operates its evaporator at 4°C and its condenser at a saturation temperature of 39.4°C. The condenser rejects its heat to the atmospheric air. Calculate the exergy destruction, in kJ, in the total system per 1000 m3 of dry air processed.

Chapter 14.7, Problem 88P, Atmospheric air at 1 atm, 32C, and 95 percent relative humidity is cooled to 24C and 60 percent

Expert Solution & Answer
Check Mark
To determine

The exergy destruction in the total system per 1000m3 of dry air.

Answer to Problem 88P

The exergy destruction in the total system per 1000m3 of dry air is 6758kJ_.

Explanation of Solution

Show the T-s diagram for the simple ideal vapour-compression refrigeration system.

Thermodynamics: An Engineering Approach, Chapter 14.7, Problem 88P

Express the mass of air.

ma=V1v1 (I)

Here, volume at state 1 is V1 and specific volume at state 1 is v1.

Express the water mass balance and energy balance equations to the combined cooling and dehumidification section.

For water mass balance:

m˙w,in=m˙w,outm˙a1ω1=m˙a2ω2+m˙wmw=ma(ω1ω2) (II)

For energy balance:

Write the energy balance equation using steady-flow equation.

E˙inE˙out=ΔE˙system (III)

Here, the rate of total energy entering the system is Ein, the rate of total energy leaving the system is Eout, and the rate of change in the total energy of the system is ΔEsystem.

Substitute 0 for ΔEsystem in Equation (III)

E˙in=E˙outm˙inhin=Q˙out+m˙outhoutQ˙out=m˙a1h1+(m˙a2h2+m˙whw)Qout=ma(h1h2)mwhw (IV)

Here, the specific enthalpy at the state 1 and 2 are h1andh2.

Write the formula for mass flow rate of refrigerant-134a.

mR=QLh1h4 (V)

Write the formula for amount of heat rejected from the condenser.

QH=mR(h2h3) (VI)

Calculate the exergy destruction in the components of the refrigeration cycle.

For the process 1-2,

Xdest,12=mRT0(s2s1)=0

Here, the process 1-2 is an isentropic.

For the process 2-3,

Xdest,23=T0(mR(s3s2)+QHTH) (VII)

For the process 3-4,

Xdest,34=mRT0(s4s3) (VIII)

Write the entropy change of water vapour in the air stream.

ΔSvapor=ma(ω2sg2ω1sg1) (IX)

Write the entropy of water leaving the cooling section.

Sw=mwsf@28°C (X)

Determine the partial pressure of water vapour at state 1 for air steam.

Pvap,1=ϕ1×Pg1=ϕ1×Psat@100°F (XI)

Determine the partial pressure of dry air at state 1 for air steam.

Pa1=P1Pvap,1 (XII)

Here, the pressure at the state 1 is P1.

Determine the partial pressure of water vapour at state 2 for air steam.

Pvap,2=ϕ2×Pg2=ϕ2×Psat@50°F (XIII)

Determine the partial pressure of dry air at state 2 for air steam.

Pa2=P2Pvap,2 (XIV)

Here, the pressure at the state 2 is P2.

Write the formula for entropy change of dry air.

ΔSa=ma(s2s1)=ma(cplnT2T1RlnPa2Pa1) (XV)

Write the formula for entropy change R-134a in the evaporator.

ΔSR,41=mR(s1s4) (XVI)

Write the formula for an entropy balance on the evaporator.

Sgen,evaporator=ΔSR,41+ΔSvapor+ΔSa+Sw (XVII)

Write the formula for an exergy destruction in the evaporator.

Xdest=T0Sgen,evaporator (XVIII)

Write the formula for the total exergy destruction.

Xdest,total=Xdest,compressor+Xdest,condenser+Xdest,throttle+Xdest,evaporator (XIX)

Conclusion:

Refer Figure A-31, “psychometric chart at 1 atm total pressure”, and write the properties corresponding to total pressure of 1 atm.

h1=106.8kJ/kgdryairω1=0.0292kgH2O/kgdryairv1=0.905m3/kgdryair

h2=52.7kJ/kgdryairω2=0.00112kgH2O/kgdryair

Refer Table A-4, “saturated water-temperature table”, and write the specific enthalpy of condensate water at temperature of 28°C using an interpolation method.

hw=hf@28°C (XX)

Here, entropy of saturation liquid at temperature of 28°C is hf@28°C.

Write the formula of interpolation method of two variables.

y2=(x2x1)(y3y1)(x3x1)+y1 (XXI)

Here, the variables denote by x and y is temperature and specific enthalpy of condensate water at state 2 respectively.

Show the specific enthalpy of condensate water at corresponding to temperature as in Table (1).

Temperature

T(°C)

Specific enthalpy of condensate water

hw@hf(kJ/kg)

25 (x1)104.83 (y1)
28 (x2)(y2=?)
30 (x3)125.74 (y3)

Substitute 25°C,28°Cand30°C for x1,x2andx3 respectively, 104.83kJ/kg for y1 and 125.74kJ/kg for y3 in Equation (XXI).

y2=(28°C25°C)(125.74kJ/kg104.83kJ/kg)(30°C25°C)+104.83kJ/kg=117.37kJ/kg117.4kJ/kg

Substitute 117.4kJ/kg for hw@hf(kJ/kg) in Equation (XX).

hw=117.4kJ/kg

Substitute 1000m3 for V1 and 0.905m3/kgdryair for v1 in Equation (I).

ma=1000m30.905m3/kgdryair=1105kg

Substitute 1105 kg for ma, 0.0292kgH2O/kgdryair for ω1, and 0.00112kgH2O/kgdryair for ω2 in Equation (II).

mw=[(1105kg)×(0.0292kgH2O/kgdryair0.00112kgH2O/kgdryair)]=(1105kg)(0.018kgH2O/kgdryair)=19.89kg

Substitute 1105 kg for ma, 106.8kJ/kg for h1, 52.7kJ/kg for h2, 19.89kg for mw, and 117.4kJ/kg for hw in Equation (IV).

Qout=[(1105kg)×(106.852.7)kJ/kg(19.89kg)×(117.4kJ/kg)]=[(1105kg)×54.1kJ/kg(19.89kg)×(117.4kJ/kg)]=[59780.5kJ(2335.086kJ)]=57,445kJ

From the Table A-11 “Saturated Refrigerant-134a-Pressure Table”, obtain the value of the specific enthalpy and entropy at state 1 of 4°C of temperature as

h1=hg@4°C=252.77kJ/kgs1=sg@4°C=0.92927kJ/kgK

Refer Table A-13 “Saturated Refrigerant-134a-Pressure Table”, and write the specific enthalpy at state 2 in 1 MPa of pressure and entropy of 0.92927kJ/kgK using an interpolation method Equation (XXI).

h2=275.29kJ/kg

From the Table A-12 “Saturated Refrigerant-134a-Pressure Table”, obtain the value of the specific enthalpy and entropy at state 3 of 39.4°C of temperature as

h3=hf@1MPa=107.32kJ/kgs3=sf@1MPa=0.39189kJ/kgK

Here, the specific enthalpy at the state 4 and 3 are equal in the throttling.

Calculate the value of x4

h4=hf+x4hfgx4=h4hfhfg (XXII)

From the Table A-11 “Saturated Refrigerant-134a-Pressure Table”, obtain the value of the specific enthalpy and entropy of saturated liquid and change upon vaporization at state 4 of 4°C of temperature as

hf=57.23kJ/kghfg=195.58kJ/kgsf=0.22381kJ/kgKsfg=0.70565kJ/kgK

Substitute 107.32kJ/kg for h4, 57.23kJ/kg for hf, and 195.58kJ/kg for hfg in Equation (XXII).

x4=107.32kJ/kg57.23kJ/kg195.58kJ/kg=50.09kJ/kg195.58kJ/kg=0.2561

Calculate the value of specific entropy of the state 4.

s4=sf+x4sfg (XXIII)

Substitute 0.22381kJ/kgK for sf, 0.70565kJ/kgK for sfg, and 0.2561 for x4 in Equation (XXIII).

s4=(0.22381kJ/kgK)+(0.2561)×(0.70565kJ/kgK)=(0.22381kJ/kgK)+(0.180717kJ/kgK)=0.4045kJ/kgK

Substitute 57,445kJ for QL, 252.77kJ/kg for h1, and 107.23kJ/kg for h3 in Equation (V).

mR=57,445kJ(252.77107.32)kJ/kg=57,445kJ145.45kJ/kg=394.9kg395kg

Substitute 395kg for mR, 275.29kJ/kg for h2, and 107.32kJ/kg for h3 in Equation (VI).

QH=(395kg)(275.29107.32)kJ/kg=(395kg)×(167.97kJ/kg)=66348kJ

Substitute 32°C for T0, 395kg for mR, 0.39189kJ/kgK for s3, 0.92927kJ/kgK for s2, and 66348kJ for QH in Equation (VII).

Xdest,23=(32°C)((395kg)(0.391890.92927)kJ/kgK+(66,348kJ)(32°C))=(32°C+273)((212.265)kJ/kgK+(66,348kJ)(32°C+273))=1607.145kJ

Substitute 32°C for T0, 395kg for mR, 0.39189kJ/kgK for s3, and 0.4045kJ/kgK for s4 in Equation (VIII)

Xdest,34=(395kg)(32°C)(0.40450.39189)kJ/kgK=(395kg)(32°C+273)(0.01261)kJ/kgK=1519kJ

Refer Table A-4 “Saturated water-temperature Table”, and write the specific entropy at state 1 at 32°C of temperature using an interpolation method Equation (XXI).

sg1=sg@32°C=8.4114kJ/kgK

Refer Table A-4 “Saturated water-temperature Table”, and write the specific entropy at state 1 at 24°C of temperature using an interpolation method Equation (XXI).

sg2=sg@24°C=8.5782kJ/kgK

Substitute 1105kg for ma, 8.4114kJ/kgK for sg1, 8.5782kJ/kgK for sg2, 0.0292kgH2O/kgdryair for ω1, and 0.00112kgH2O/kgdryair for ω2 in Equation (IX).

ΔSvapor=(1105kg)(0.00112kgH2O/kgdryair×8.5782kJ/kgK0.0292kgH2O/kgdryair×8.4114kJ/kgK)=[(1105kg)(0.096076kJ/kgK0.245613kJ/kgK)]=(1105kg)(0.14954kJ/kgK)=165.238kJ/K

Substitute 19.89kg for mw and 0.4091kJ/kgK for sf@28°C in Equation (X).

Sw=(19.89kg)×(0.4091kJ/kgK)=8.136kJ/K8.14kJ/K

Substitute 0.95 for ϕ1 and 4.760kPa for Psat@32°C in Equation (XI).

Pvap,1=(0.95)×(4.760kPa)=4.522kPa

Substitute 101.325kPa for P1 and 4.522kPa for Pvap,1 in Equation (XII).

Pa1=(101.3254.522)kPa=96.80kPa

Substitute 0.60 for ϕ2 and 2.986kPa for Psat@50°F in Equation (XIII).

Pvap,2=(0.60)×(2.986kPa)=1.792kPa

Substitute 101.325kPa for P2 and 1.792kPa for Pvap,2 in Equation (XIV).

Pa2=(101.3251.792)kPa=99.53kPa

Substitute 1105kg for ma, 1.005 for cp, 4°C for T2, 32°C for T1, 0.287kJ/kgK for R, 99.53kPa for Pa,2, and 96.80kPa for Pa1 in Equation (XV).

ΔSa=(1105kg)×[(1.005)ln4°C32°C(0.287)ln99.53kPa96.80kPa]=(1105kg)×[(1.005)ln4°C+27332°C+273(0.287)ln99.53kPa96.80kPa]=(1105kg)×[(1.005)ln(0.908197)(0.287)ln(1.028202kPa)]=38.34kJ/kgdryair

Substitute 395kg for mR, 0.92927kJ/kgK for s1, and 0.4045kJ/kgK for s4 in Equation (XVI).

ΔSR,41=(395kg)(0.929270.4045)kJ/kgK=(395kg)(0.52477kJ/kgK)=207.28kJ/K207.3kJ/K

Substitute 207.3kJ/K for ΔSR,41, 165.2kJ/K for ΔSvapor, 38.34kJ/K for ΔSa, and 8.14kJ/K for Sw in Equation (XVII).

Sgen,evaporate=(207.3+(165.2)+(38.34)+8.14)kJ/K=11.90kJ/K

Substitute 32°C for T0 and 11.90kJ/K for Sgen,evaporate in Equation (XVIII).

Xdest=(32°C)(11.90kJ/K)=(32°C+273)(11.90kJ/K)=3630kJ

Substitute 0 for Xdest,compressor, 1609kJ for Xdest,condenser, 1519kJ for Xdest,throttle, and 3630KJ for Xdest,evaporator in Equation (XIX).

Xdest,total=(0+1609+1519+3630)kJ=6758kJ

Thus, the exergy destruction in the total system per 1000m3 of dry air is 6758kJ_.

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Chapter 14 Solutions

Thermodynamics: An Engineering Approach

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