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 8.8, Problem 66P

a)

To determine

The rate of exergy destroyed during the process and the exit temperature (T4) of the air when the outer surface of air conditioner is insulated.

a)

Expert Solution
Check Mark

Answer to Problem 66P

The rate of exergy destroyed during the process is 0.594kW_.

The exit temperature (T4) of the air is 257.2Kor(15.8°C)_.

Explanation of Solution

Draw the schematic diagram of the flow of refrigerant-134a through evaporator section as shown in Figure (1).

Thermodynamics: An Engineering Approach, Chapter 8.8, Problem 66P

Write the expression for the mass balances equation for the heat exchanger.

m˙inm˙out=Δm˙system

Here, mass flow rate of refrigerant at inlet is m˙in, mass flow rate of refrigerant at outlet is m˙out, and net mass flow rate of refrigerant through system is Δm˙system.

Since net mass flow rate of refrigerant-134a and air through system is 0.

m˙inm˙out=0

From Figure (1), the mass flow rate of refrigerant-134a at state1and2 is equal.

m˙1=m˙2=m˙R (I)

Here, initial and final mass flow rate of refrigerant at state1and2 is m˙1andm˙2 respectively, and mass flow rate of refrigerant is m˙R.

From Figure (1), the mass flow rate of air at state3and4 is equal.

m˙3=m˙4=m˙a (II)

Here, mass flow rate of air at state3and4 is m˙3andm˙4 respectively, and mass flow rate of air is m˙a.

Write the expression for the enthalpy at state 1 (h1).

h1=hf+x1hfg (III)

Write the expression for the entropy at state 1(s1).

s1=sf+x1sfg (IV)

Write the expression for the mass flow rate of air (m˙a).

m˙a=P3V˙3RT3 (V)

Here, gas constant of air is R, temperature at state 3 is T3, pressure at state 3 is P3, and volume flow rate of air at state 3 is V˙3.

Write the expression for energy balance for the heat exchanger

E˙inE˙out=ΔE˙system (VI)

Here, rate of net energy transfer in to the control volume is E˙in, rate of net energy transfer exit from the control volume is E˙out and rate of change in internal energy of system is ΔE˙system.

Substitute 0 for ΔE˙system in Equation (VI), and re-write the energy balance as follows:

E˙inE˙out=0E˙in=E˙outm˙1h1+m˙3h3=m˙2h2+m˙4h4m˙2h2m˙1h1=m˙3h3m˙4h4

m˙2(h2h1)=m˙3(h3h4)m˙R(h2h1)=m˙a(h3h4)=m˙acp(T3T4)T4=T3m˙R(h2h1)m˙acp (VII)

Here, mass flow rate at state1,2,3and4 is m˙1,m˙2,m˙3andm˙4 respectively, enthalpy at state1,2,3and4 is h1,h2,h3andh4 respectively, constant pressure specific heat of air at room temperature is cp, temperature at state3and4 is T3andT4 respectively.

Write the expression for the entropy balance for the steady flow system as;

S˙inS˙out+S˙gen=ΔS˙system (VIII)

Here, rate of entropy generation is S˙gen, rate of change in entropy is ΔS˙system, rate of entropy at inlet condition is S˙in, and rate of entropy at outlet condition is S˙out.

At steady state, rate of change in entropy of the system is zero.

Substitute 0 for ΔS˙system in Equation (VIII), and re-write the entropy balance as follows:

S˙inS˙out+S˙gen=0m˙1s1+m˙3s3m˙2s2+m˙4s4+S˙gen=0m˙Rs1+m˙as3m˙Rs2+m˙as4+S˙gen=0S˙gen=m˙R(s2s1)+m˙a(s4s3) (IX)

Here, entropy at state1,2,3and4 is s1,s2,s3ands4 respectively.

Write the expression for the change between state 4 entropy (s4) and state 3 entropy (s3).

s4s3=cpln(T4T3)Rln(P4P3) (X)

Here, temperature at state 3and4 is T3andT4 and pressure at state 3and4 is P4andP3.

Write the expression for the exergy destroyed rate during the process (X˙destroyed).

X˙destroyed=T0S˙gen (XI)

Here, dead state temperature is T0.

Conclusion:

Refer to Table A-12, “Saturated refrigerant-134a-Pressure table”, obtain the following properties at the pressure (P1) of 120kPa and state 1 quality (x1) of 0.3 as;

hf=22.47kJ/kghfg=214.52kJ/kgsf=0.09269kJ/kgKsfg=0.85520kJ/kgK

Here, enthalpy of saturated liquid is hf, enthalpy of evaporation is hfg, entropy of saturated liquid is sf and entropy of evaporation is sfg.

Substitute 22.47kJ/kg for hf, 0.3 for x1 and 214.52kJ/kg for hfg in equation (III)

h1=(22.47kJ/kg)+(0.3)(214.52kJ/kg)=22.47kJ/kg+64.356kJ/kg=86.83kJ/kg

Substitute 0.09269kJ/kgK for sf, 0.3 for x1 and 0.85520kJ/kgK for sfg in equation (IV).

s1=(0.09269kJ/kgK)+(0.3)(0.85520kJ/kgK)=0.09269kJ/kgK+0.25656kJ/kgK=0.34925kJ/kgK

Refer to Table A-12, “Saturated refrigerant-134a-Pressure table”, obtain the following properties at the pressure (P1) of 120kPa and quality is saturated vapor as;

h2,hg@120kPa=236.99kJ/kgs2,sg@120kPa=0.94789kJ/kgK

Here, enthalpy at state 2 is h2, entropy at state 2 is s2, enthalpy of saturated vapor is hg and entropy of saturated vapor is sg.

From the Table A-2, “Ideal-gas specific heats of various common gases table”, select the gas constant of air gas (R) as 0.287kPam3/kgK.

Substitute 100kPa for P3, 6m3/min for V˙3, 0.287kPam3/kgK for R and 27°C for T3 in equation (V).

m˙a=(100kPa)(6m3/min)(0.287kPam3/kgK)(27°C)=(100kPa)(6m3/min)(0.287kPam3/kgK)(27+273)K=(100kPa)(6m3/min)(0.287kPam3/kgK)(300K)=6.969kg/min

At steady state, rate of change in internal energy of the system is zero.

From the Table A-2, “Ideal-gas specific heats of various common gases table”, select the constant pressure specific heat (cp) of air as 1.005kJ/kg°C.

Substitute 1.005kJ/kg°C for cp, 27°C for T3, 236.99kJ/kg for h2, 86.83kJ/kg for h1, and 6.969kg/min for m˙a and 2kg/min for m˙R in Equation (VII).

T4=(27°C)(2kg/min)(236.9986.83)kJ/kg(6.969kg/min)(1.005kJ/kg°C)=27°C300.32kJ/min7.0038kJ/min°C=27°C42.879°C=15.8°C

=(15.8+273)K=257.2K

Thus, the exit temperature (T4) of the air is 257.2Kor(15.8°C)_.

Substitute 1.005kJ/kgK for cp, 257.2K for T4, 27°C for T3, 0.287kPam3/kgK for R, 0 for P4, and 100kPa for P3 in Equation (X).

s4s3=(1.005kJ/kgK)ln(257.2K27°C)(0.287kPam3/kgK)ln(0100kPa)=(1.005kJ/kgK)ln[257.2K(27+273)K]0=(1.005kJ/kgK)[ln(257.2K300K)]=0.1550kJ/kgK

Substitute 2kg/min for m˙R, 6.969kg/min for m˙a, 0.1550kJ/kgK for s4s3, 0.94789kJ/kgK for s2 and 0.34925kJ/kgK for s1 in Equation (IX) to get S˙gen.

S˙gen={(2kg/min)[(0.947890.34925)kJ/kgK]+(6.969kg/min)(0.1550kJ/kgK)}=1.19728kJ/minK1.0801kJ/minK=0.1170kJ/minK

Substitute 32°C for T0 and 0.1170kJ/minK for S˙gen in Equation (XI).

X˙destroyed=(32°C)(0.1170kJ/minK)=(32+273)K(0.1170kJ/minK)=(305K)(0.1170kJ/minK)=35.685kJ/min(1min60s)

=0.594kJ/s(kWkJ/s)=0.594kW

Thus, the rate of exergy destroyed during the process is 0.594kW_.

b)

To determine

The exit temperature of the air and the rate of exergy destroyed during the process without insulation.

b)

Expert Solution
Check Mark

Answer to Problem 66P

The exit temperature of the air without insulation is 261.4K or (11.6°)_.

The rate of exergy destroyed during the process without insulation is 0.68kW_.

Explanation of Solution

Write the expression for the state 4 temperature (T4) from steady-flow energy equation.

Q˙in=m˙R(h2h1)+m˙acp(T4T3)T4=T3+Q˙inm˙R(h2h1)m˙acp (XII)

Here, heat gain is from the surrounding Q˙in.

Write the expression for the entropy balance For an extended system as;

S˙inS˙out+S˙gen=ΔS˙systemQ˙inT0+m˙1s1+m˙3s3m˙2s2+m˙4s4+S˙gen=0Q˙inT0+m˙Rs1+m˙as3m˙Rs2+m˙as4+S˙gen=0S˙gen=m˙R(s2s1)+m˙a(s4s3)Q˙inT0 (XIII)

Conclusion:

Substitute 27°C for T3, 30kJ/min for Q˙in, 2kg/min for m˙R, 236.99kJ/kg for h2, 86.83kJ/kg for h1, 6.969kg/min for m˙a and 1.005kJ/kg°C for cp in Equation (XII) to get T4.

T4=27°C+30kJ/min[(2kg/min)(236.9986.83)kJ/kg](6.969kg/min)(1.005kJ/kg°C)=27°C+30kJ/min300.32kJ/min7.0038kg/min°C=27°C38.59°C=11.6°C

=(11.6+273)K=261.4K

Thus, the exit temperature of the air is 261.4K or (11.6°)_.

substitute 1.005kJ/kgK for cp, 261.4K for T4, 27°C for T3, 0.287kPam3/kgK for R, 0 for P4, and 100kPa for P3 in Equation (XIII).

s4s3=(1.005kJ/kgK)ln(261.4K27°C)(0.287kPam3/kgK)ln(0100kPa)=(1.005kJ/kgK)ln[261.4K(27+273)K]0=(1.005kJ/kgK)[ln(261.4K300K)]

=0.1384kJ/kgK

Substitute 30kJ/min for Q˙in, 2kg/min for m˙R, 6.969kg/min for m˙a, 0.94789kJ/kgK for s2 and 0.34925kJ/kgK for s1, 0.1384kJ/kgK for s4s3, and 27°C for T0 in Equation (XIII) to get S˙gen.

S˙gen={(2kg/min)[(0.947890.34925)kJ/kgK]+(6.969kg/min)(0.1384kJ/kgK)30kJ/min27°C}=1.19728kJ/minK0.9645kJ/minK30kJ/min300K=1.19728kJ/minK0.9645kJ/minK0.1kJ/minK=0.13278kJ/minK

Substitute 32°C for T0 and 0.13278kJ/minK S˙gen in Equation (XI).

X˙destroyed=T0S˙gen=(32°C)(0.13278kJ/minK)=(32+273)K(0.13278kJ/minK)=(305K)(0.13278kJ/minK)

=40.5kJ/min(1min60s)=0.68kJ/s(kWkJ/s)=0.68kW

Thus, the rate of exergy destroyed during the process is 0.68kW_.

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Chapter 8 Solutions

Thermodynamics: An Engineering Approach

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