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Material Type: Exam; Class: Thermodynamics and Statistical Mechanics; Subject: Physics; University: University of Colorado - Boulder; Term: Fall 2008;
Typology: Exams
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Physics 4230, Fall 2008, Midterm Exam 2, Solutions
1 T
N,V
= slope of S(U ). (1)
Since system B has a smaller slope of S(U ), it has a larger temperature. (b) Here, Q is the heat flowing from the hotter system to the colder one. So, it’s the heat flowing from B to A. We define QA to be the heat added to A, and QB the heat added to B. We have QA = Q, and QB = −Q. The change in entropy of system A is
U=UA
U=UA
The partial derivative is evaluated at constant N and V (not explicitly written above), and it’s evaluated at U = UA. Similarly, the change in entropy of B is
U=UB
U=UB
So the total change in entropy is
U=UA
U=UB
dU = T dS − P dV. (5)
Now, since the temperature is held constant during this process, the energy U doesn’t change, since the energy of a diatomic ideal gas is just U = (5/2)N kT. Therefore we can set dU = 0. Since we’re interested in the change in entropy, we can solve the thermodynamic identity for dS:
dS =
dV =
N kT V
dV =
N k V
dV. (6)
In the second equality above, I used the ideal gas law to plug in P = N kT /V. Let’s get the change in entropy for the gas on the left and right separately (∆SL and ∆SR), and then add them up to get the final answer. We find the entropy change by integrating dS from the initial to the final volume. For the gas on the left, the initial volume is V and the final volume is 5V , so
∫ (^) Vf
Vi
dS =
V
N k V
dV = N k
V
dV V
= N k ln(V )
5 V V
= N k
ln(5V ) − ln(V )
= N k ln
= N k ln 5. (8)
For the gas on the right, everything is the same, except now the initial volume is 9V and the final volume is 5V. So we have
∆SR = N k
9 V
dV V =^ N k
ln(5V ) − ln(9V )
= N k ln(5/9). (9)
The total change in entropy is
∆S = ∆SL + ∆SR = N k
ln 5 + ln(5/9)
= N k ln(25/9). (10)
(c) Since temperature is held constant, we have
∆F = ∆U − T ∆S. (11)
We already showed ∆U = 0 in part (a), and in part (b) we found ∆S = N k ln(25/9). Therefore we have
∆F = −N kT ln(25/9). (12)
(d) The change in entropy is the same as it was in part (b), ∆S = N k ln(25/9). The reason is that, here, the initial and final states of the gas are the same as they were in part (b). Since entropy only depends on the state of a system, the change in entropy only depends on the initial and final states, not on how one gets between them.
ec =
Qh 1
Qc 2 W =^
Qc 2 Qh 1 = COP,^ (13)
the COP of the combined refrigerator. Now, from the discussion in class and in Schroeder, we know
e ≤ emax = 1 −
Tc 1 Th 1
c ≤ cmax =
Tc 2 Th 2 − Tc 2
Therefore,
COP ≤ COPmax = emaxcmax =
1 − Tc^1 Th 1
) (^) Tc 2 Th 2 − Tc 2
dUR = TRdSR − PRdVR + μRdNR = TRdSR + μRdNR. (17)
Because the reservoir does not exchange volume with the system, we took dVR = 0 in the second equality.