Example Problem with Complete Solution

4F-5 : Performance of an Ideal Gas Cycle
10 pts
An ideal gas, initially at 30°C and 100 kPa, undergoes an internally reversible, cyclic process in a closed system.  The gas is first compressed adiabatically to 500 kPa, then cooled at a constant pressure of 500 kPa to 30°C, and finally expanded isothermally to its original state.
                   
a.) Carefully draw this process in a traditional piston-and-cylinder schematic.
                   
b.) Sketch the process path for this cycle on a PV Diagram.  Put a point on the diagram for each state.  Be sure to include and label all the important features for a complete PV diagram for this system.
 
                   
c.) Calculate Q, W, ΔU and ΔH, in J/mole, for each step in the process and for the entire cycle. Assume that CP = (7/2) R.
 
                   
d.) Is this cycle a power cycle or a refrigeration cycle ?  Explain.  Calculate the thermal efficiency or COP of the cycle, whichever is appropriate.
 
                   
Read : Sketch carefully.  Understanding what is going on in the problem is half the battle.  Apply the 1st Law, the definitions of boundary work, CP and CV to a cycle on an ideal gas with constant heat capacities.  Take advantage of the fact that step 1-2 is both adiabatic and reversible, so it is isentropic.  Power cycles produce a net amount of work and proceed in a clock-wise direction on a PV Diagram.  
Given : T1
303.15
K P1
100
kPa
T2
???
K P2
500
kPa
T3
303.15
K P3
500
kPa
Q12
0
J/mole R
8.314
J/mole-K
CP
29.099
J/mole-K
Find : For each of the three steps and for the entire cycle: ΔU
???
J/mole
  ΔH
???
J/mole
  Q
???
J/mole
    W
???
J/mole
Diagrams :
Part a.) Figure 1.
Part b.) Figure 2.
Assumptions:
  1. Step 1-2 is adaibatic, Step 2-3 is isobaric, Step 3-1 is isothermal.
  2. The entire cycle and all of the steps in the cycle are internally reversible.
  3. Changes in kinetic and potential energies are negligible.Changes in kinetic and potential energies are negligible.
  4. Boundary work is the only form of work interaction during the cycle.
  5. The PVT behavior of the system is accurately described by the ideal gas EOS.
Equations / Data / Solve :
Part c.) Let's begin by analyzing step 1-2, the adiabatic compression.
Begin by applying the 1st law for closed systems to each step in the Carnot Cycle.  Assume that changes in kinetic and potential energies are negligible.
Equation. Eqn 1
Because internal energy is not a function of pressure for an ideal gas, we can determine DU by integrating the equation which defines the constant volume heat capacity.  The integration is simplified by the fact that the heat capacity for the gas in this problem has a constant value.
   
Equation. Eqn 2 Equation. Eqn 3
Combining Eqns 1 & 3 yields: Equation. Eqn 4
The problem is that we do not know T2.  So, our next task is to determine T2.
Since the entire cycle is reversible and this step is also adiabatic, this step is isentropic.
The fastest way to determine T2 is to use one of the PVT relationships for isentropic processes.
 
Equation. Eqn 5
Solve Eqn 5 for T2: Equation. Eqn 6
Now, we need to evaluate γ : Equation. Eqn 7
But for ideal gases : Equation. Eqn 8
Solving Eqn 8 for CV yields : Equation. Eqn 9
Plugging values into Eqn 9 and then Eqn 7 yields : CV
20.785
J/mole-K
γ
1.4
Now, plug values into Eqn 5 to get T2
and plug that into Eqn 4 to get W12 :
T2
480.13
K
W12
-3678.6
J/mole
Plugging values into Eqn 1 yields : ΔU12
3678.6
J/mole
Now, we can get ΔH
from its definition :
Equation. Eqn 10
But, the gas is an ideal gas: Equation. Eqn 11
Combining Eqns 10 & 11 gives us : Equation. Eqn 12
Now, we can plug values into Eqn 12 : ΔH12
5150.1
J/mole
Next, let's analyze step 2-3, isobaric cooling.
T2
480.1349
K P2
500
kPa
T3
303.15
K P3
500
kPa
The appropriate form of the 1st Law is: Equation. Eqn 13
Because we assumed that boundary work is the only form of work that crosses the system boundary, we can determine work from its definition.
 
Equation. Eqn 14 Isobaric process: Equation. Eqn 15
Because the system contains and ideal gas: Equation. Eqn 16
W23
-1471.5
J/mole
     
Next we can calculate ΔU by applying Eqn 3 to step 2-3: Equation. Eqn 17
ΔU23
-3678.6
J/mole
Now, solve Eqn 13 to
determine Q23 :
Equation. Eqn 18
Q23
-5150.1
J/mole
   
Now, we apply Eqn 12 to
step 2-3 to determine ΔH :
Equation. Eqn 19
ΔH23
-5150.1
J/mole
Next, we analyze step 3-1, isothermal expansion.
For ideal gases, U and H are
functions of T only.  Therefore :
ΔU31
0.0
J/mole
  ΔH31
0.0
J/mole
The appropriate form
of the 1st Law is:
Equation. Eqn 20
Again, because we assumed that boundary work is the only form of work that crosses the system boundary, we can determine work from its definition.
   
Equation. Eqn 21 Ideal Gas EOS : Equation. Eqn 22
Solve Eqn 22 for P and
substitute the result into
Eqn 21 to get :
Equation.
Eqn 23
Equation. Eqn 24
Integrating Eqn 24 yields : Equation. Eqn 25
We can use the Ideal Gas EOS to avoid calculating V1 and V3 as follows:
Apply Eqn 22 to both states 3 and 1 : Equation. Eqn 26
Cancelling terms and rearranging leaves : Equation. Eqn 27
Use Eqn 27 to eliminate the V's from Eqn 25 : Equation. Eqn 28
Now, plug values into Eqn 28 and then Eqn 20 : W31 4056.4 J/mole
Q31 4056.4 J/mole
Finally, we can calculate Qcycle and Wcycle from :
   
Equation. Eqn 29 Equation. Eqn 30
Plugging values into Eqns 29 & 30 yields : Wcycle
-1093.7
J/mole
Qcycle
-1093.7
J/mole
This result confirms what an application of the 1st Law to the entire cycle tells us:
Qcycle = Wcycle.
Part d.) The cycle is a refrigeration cycle because both Wcycle and Qcycle  are negative.
The coefficient of performance of a refrigeration cycle is defined as : Equation. Eqn 31
QC is the heat absorbed by the system during the cycle. In this case, QC =Q31.
W is the work input to the system during the cycle. In this case, W = - Wcycle.
Therefore : QC
4056.4
J/mole
W
1093.7
J/mole
Plug values into Eqn 31 to get : COPR 3.709
Verify : The ideal gas assumption needs to be verified.  
We need to determine the specific
volume at each state and check if :
  Equation. Eqn 32
 
V1
25.20
L/mol Equation. Eqn 33
V2
7.98
L/mol
V3
5.04
L/mol
The specific volume at each state is greater than 5 L/mol for all states and Air can be considered to be a diatomic gas, so the ideal gas assumption is valid.
Answers: a.) See diagram above. b.) See diagram above.
c.)
Step
ΔU
ΔH
Q
W
 
1 - 2
3679
5150
0
-3679
All values in this table are in J/mole.
 
2 - 3
-3679
-5150
-5150
-1471
 
3 - 1
0
0
4056
4056
 
Cycle
0
0
-1094
-1094
d.) Refrigeration or Heat Pump Cycle.
COPR
3.7
COPHP 4.7
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