Entropy For Irrevesible Process

In summary, the conversation discusses the transfer of heat between two 100g aluminum cubes at different temperatures and the resulting change in entropy. The specific heat of aluminum and the temperatures before and after the heat transfer are provided. The conversation also touches upon the use of the Clausius inequality in evaluating entropy changes.
  • #1
morrobay
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Homework Statement


Two 100g Aluminum cubes with T1 = 80° C and T2 = 20°C
Specific heat of Al is .22 cal/g/°C. The cubes are placed in contact and in short period of time
a quantity of heat, dQ , is transferred from T1 cube to T2 cube.
The cubes temperatures now are 75°C and 25°C. After a little math : dQ = 640 Joules
The total entropy of the two cubes before dQ was: 22.3 J/K and after dQ was 27.5 J/K

Homework Equations


S2-S1 > ∫12 dQ/T
ΔS = 5.2 J/K > ∫12 dQ/T This should be evaluated :
ln dQ/T - ln dQ/T . The question on this is what are the T values here ?
Is it necessary to do two evaluations, one for hotter object and another for cooler object ?
,




The Attempt at a Solution


S2-S1 = 5.2J/K
For hotter object ln 460 J/348K - ln 460J/353K = .01
For cooler object ln 460J/293K - ln 460J/298K = .02
 
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  • #2
Throughout the heat interchange, the temperature at the interface between the two cubes was 50C = 323 K. For an irreversible processes, if you are evaluating dQ/T for testing the Clausius inequality, you use the temperature at the boundary (interface). What was the integral of dQ/T for the hotter body? What was the integral of dQ/T for the colder body? What was the sum of these? How does that compare with the actual entropy change?
 
  • #3
In the attempt of solution above is the evaluation of integral for hotter and cooler object correct ?
Total entropy change was + 5.2J/K
dQ/T for 323 K = 640 J/323K = 1.98 J/K

The inequality certainly holds , my question is whether I evaluated the two integrals correctly
with temperatures before and after dQ for both objects.
S2-S1 = 5.2J/K > 1.98 J/K (.03 )
 
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  • #4
morrobay said:
In the attempt of solution above is the evaluation of integral for hotter and cooler object correct ?
Total entropy change was + 5.2J/K
dQ/T for 323 K = 640 J/323K = 1.98 J/K

The inequality certainly holds , my question is whether I evaluated the two integrals correctly
with temperatures before and after dQ for both objects.
S2-S1 = 5.2J/K > 1.98 J/K (.03 )

No. For the hotter body, the dQ/T is -640/323 = -1.98. For the colder body dQ/T is +640/323 = +1.98. So, the total dQ/T for both bodies is zero. This is the value that you are supposed to compare with the sum of the actual entropy changes for the two bodies, which is

[tex]ΔS=mC_v(\ln (348/353)+\ln (298/293))[/tex]
 
  • #5
Chestermiller said:
No. For the hotter body, the dQ/T is -640/323 = -1.98. For the colder body dQ/T is +640/323 = +1.98. So, the total dQ/T for both bodies is zero. This is the value that you are supposed to compare with the sum of the actual entropy changes for the two bodies, which is

[tex]ΔS=mC_v(\ln (348/353)+\ln (298/293))[/tex]

With m = mass = 200g and Cv= specific heat Al = .22cal/g/C
ΔS = 200g*.92J/g/C * ln 348/353 + ln 298/293 = .48J/K
Good news , with math correction total entropy change for both objects S2 - S1 =
27.54J/K - 27.11J/k = .43J/K This value ( see work below ) is very close to above value
arrived at independently

Example for entropy , Q/T, for 100g object at 80 C , specific heat = .92J/g/C before dQ , S1
100g*80 C * .92J/g/C = 7360 J/353K = 20.84J/K + 6.27J/K for 20c object = 27.11J/K
 
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  • #6
ΔShot=92ln(348/353)=-1.05 J/K

ΔScold=92ln(298/293)=+1.55 J/K

(dQ/T)hot=-(92)(5)/323=-1.43 J/K

(dQ/T)cold=+(92)(5)/323=+1.43 J/K

The inequality must be satisfied not only for the system of two masses as a whole, but also for each mass individually. For the system as a whole,

ΔShot+ΔScold=-1.05 +1.55=0.50 J/K

(dQ/T)hot+(dQ/T)cold=-1.43+1.43=0 J/K

For the hot mass:
-1.05>-1.43

For the cold mass:
1.55>+1.43
 
  • #7
As I said in the other forum, you are generally right that T may not even be defined during an irreversible process. I think here you are supposed to assume that the thermal bridge between the two cubes has much lower heat conductance than the aluminium blocks. Then the temperature within the blocks is homogeneous and you can relate it to dQ=C_v dT.
 
  • #8
DrDu said:
As I said in the other forum, you are generally right that T may not even be defined during an irreversible process. I think here you are supposed to assume that the thermal bridge between the two cubes has much lower heat conductance than the aluminium blocks. Then the temperature within the blocks is homogeneous and you can relate it to dQ=C_v dT.

Not really. If the interface is infinitely conductive, then, by symmetry, the temperature at the interface would have to be 50 C throughout the heat exchange in this problem. If you could not be sure what the temperature at the interface would be in any irreversible process, then the temperature in Clausius' inequality would be meaningless, except for a reversible process, in which case the equality would apply.

Chet
 
  • #9
Chestermiller said:
Not really. If the interface is infinitely conductive, then, by symmetry, the temperature at the interface would have to be 50 C throughout the heat exchange in this problem. If you could not be sure what the temperature at the interface would be in any irreversible process, then the temperature in Clausius' inequality would be meaningless, except for a reversible process, in which case the equality would apply.

Chet
I have not seen the Clausius inequality used in this way. The Clausius inequality relates to a cyclical process.

Since entropy is a state function, when the system returns to its original state there is no change in entropy: ΔSsys = ∫dQrev/T = 0.

However, if the cycle is not reversible ∫dQ/T ≤ 0 over the entire cycle where dQ is the actual heat flow into/out of the system (ie. this is strictly a path function, not a state function). This is because for a given amount of heat flow into the system, less work is done than in the reversible case so there is more heat flow out of the system to the cold reservoir than in the reversible case. This makes ∫dQ/T < ∫dQrev/T.

AM
 
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  • #10
Andrew Mason said:
I have not seen the Clausius inequality used in this way. The Clausius inequality relates to a cyclical process.

Since entropy is a state function, when the system returns to its original state there is no change in entropy: ΔSsys = ∫dQrev/T = 0.

However, if the cycle is not reversible ∫dQ/T ≤ 0 over the entire cycle where dQ is the actual heat flow into/out of the system (ie. this is strictly a path function, not a state function). This is because for a given amount of heat flow into the system, less work is done than in the reversible case so there is more heat flow out of the system to the cold reservoir than in the reversible case. This makes ∫dQ/T < ∫dQrev/T.

AM

The form of the Clausius inequality that I am used to is
[tex]dS≥dQ/T[/tex]
There have been numerous recent references to this form of the Clausius inequality on PF.

Chet
 

Related to Entropy For Irrevesible Process

1. What is entropy for irreversible processes?

Entropy for irreversible processes is a measure of the degree of disorder or randomness in a system. It is often described as a measure of the energy that is unavailable for work in a system.

2. How is entropy different for irreversible processes compared to reversible processes?

Entropy for irreversible processes increases over time, while for reversible processes it remains constant. This is because irreversible processes result in a net increase in disorder, while reversible processes do not.

3. How is entropy related to the second law of thermodynamics?

The second law of thermodynamics states that the total entropy of a closed system will always increase over time. This means that for irreversible processes, the total entropy of the system will increase, while for reversible processes it will remain constant.

4. Can entropy be negative for irreversible processes?

No, entropy cannot be negative for irreversible processes. This is because entropy is a measure of disorder and disorder cannot have a negative value. However, for reversible processes, entropy can be both positive and negative.

5. What are some real-life examples of irreversible processes and their impact on entropy?

Examples of irreversible processes include the burning of fuel, the diffusion of gas, and the mixing of two substances. These processes result in an increase in entropy, as they lead to a more disordered state. This can be seen in the release of heat and the dispersal of particles in these processes.

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