Gas at a constant pressure: using Cv.dT correctly

Click For Summary

Homework Help Overview

The discussion revolves around the application of the equation for internal energy change (dU) in the context of a gas at constant pressure, specifically focusing on the use of Cv*dT. Participants are exploring the implications of sign conventions and the correct interpretation of temperature changes in this context.

Discussion Character

  • Conceptual clarification, Assumption checking, Mathematical reasoning

Approaches and Questions Raised

  • Participants discuss the order of temperatures in the dT calculation and its impact on sign conventions. There are inquiries about the relationship between dU, dW, and dQ in different processes, particularly adiabatic and isobaric. Some participants express confusion regarding the overlap of these quantities and seek clarification on the underlying principles.

Discussion Status

The conversation is ongoing, with participants providing insights and corrections to each other's reasoning. Some guidance has been offered regarding the correct interpretation of the first law of thermodynamics and the implications of different sign conventions. Multiple interpretations of the processes are being explored, and participants are actively questioning their assumptions.

Contextual Notes

Participants are navigating the complexities of thermodynamic processes, including adiabatic and isobaric conditions, while adhering to homework constraints. There is a focus on understanding the definitions and relationships between heat, work, and internal energy changes without reaching definitive conclusions.

chopnhack
Messages
53
Reaction score
3
Hello, my questions is not so much homework, but a request for a definition. When we use Cv*dT to solve for dU (internal energy) in a constant pressure example, what is the order of the temperatures entered into dT?
Is one to assume its final temp minus initial temp? I ask because it leads to sign convention and I want to make sure I understand it properly.

Thanks!
 
Physics news on Phys.org
Yes, dT represents final temperature minus initial temperature for an infinitesimal change in temperature.

Positive dT corresponds to a temperature increase, which also corresponds to an increase in internal energy of the gas. It doesn't matter whether the pressure is constant or not.
 
  • Like
Likes   Reactions: chopnhack
Thank you, that helped me a lot!

Could you point me in the right direction for the last part of this problem? I tried to simply sum up the dQ's, dU's and dW's, but noticed that there was overlap where in some cases dU = dW... I then thought out the process and how the gas starts at a certain temperature and pressure, the gas loses heat while expanding and regains said heat while contracting. I thought that they might cancel each other out. The gas returns to its original starting point, temperature and pressure - no net W done.

Thanks in advance.
 

Attachments

  • 2.pdf
    2.pdf
    101.4 KB · Views: 966
chopnhack said:
Thank you, that helped me a lot!

Could you point me in the right direction for the last part of this problem? I tried to simply sum up the dQ's, dU's and dW's, but noticed that there was overlap where in some cases dU = dW... I then thought out the process and how the gas starts at a certain temperature and pressure, the gas loses heat while expanding and regains said heat while contracting. I thought that they might cancel each other out. The gas returns to its original starting point, temperature and pressure - no net W done.

Thanks in advance.
In step 1, ##\Delta U## is negative, since the temperature decreased. If you correct this, then you will find that ##\Delta U## for the cycle is equal to zero. You should also then find that W for the cycle is equal to Q for the cycle.
 
  • Like
Likes   Reactions: chopnhack
Chestermiller said:
In step 1, ##\Delta U## is negative, since the temperature decreased. If you correct this, then you will find that ##\Delta U## for the cycle is equal to zero. You should also then find that W for the cycle is equal to Q for the cycle.
I was close!
I missed the fact that the calculation was final temperature minus initial temperature for dT which yielded the negative value for dU and dW for process one.

Process 1: Adiabatic

dQ = 0 No heat added in an Adiabatic expansion, the gas expands using internal energy.

dU = dW = Cv×dT = 12.471 JK-1 × (389K-588K) --> -2,482 J

But now that I look at the other parts, my process for isobaric would need to yield a positive value to have the whole system balance out with 993J Q and W
My understanding of the equation was that final volume minus initial volume in this case will yield a negative value...
Where have I gone wrong?

Process 2: Isobaric

W = P(V2-V1)--> 3.59x10^4Pa (0.0484m3- 0.0899m3) --> -1,490 J work done on the gas - final volume is less.

dU = Cv×dT à 12.471 JK-1 × (209.4K-389K) = -2,239 J

dQ = -2,239 J + -1,490 J = -3,729 J
 
chopnhack said:
I was close!
I missed the fact that the calculation was final temperature minus initial temperature for dT which yielded the negative value for dU and dW for process one.

Process 1: Adiabatic

dQ = 0 No heat added in an Adiabatic expansion, the gas expands using internal energy.

dU = dW = Cv×dT = 12.471 JK-1 × (389K-588K) --> -2,482 J

No. $$\Delta U=Q-W$$so, if Q = 0, $$W=-\Delta U=+2482 J$$
But now that I look at the other parts, my process for isobaric would need to yield a positive value to have the whole system balance out with 993J Q and W
My understanding of the equation was that final volume minus initial volume in this case will yield a negative value...
Where have I gone wrong?

Process 2: Isobaric

W = P(V2-V1)--> 3.59x10^4Pa (0.0484m3- 0.0899m3) --> -1,490 J work done on the gas - final volume is less.

dU = Cv×dT à 12.471 JK-1 × (209.4K-389K) = -2,239 J

dQ = -2,239 J + -1,490 J = -3,729 J
Process 2 calc is correct.
 
  • Like
Likes   Reactions: chopnhack
Chestermiller said:
No. $$\Delta U=Q-W$$so, if Q = 0, $$W=-\Delta U=+2482 J$$

Process 2 calc is correct.
Ok, I see the manipulation, simply restating the Q=U+W equation, solve for U instead. What would lead me to do that though? The lecture notes showed us many derivations and the one that came to mind when solving this problem was dU = dW = Cv×dT (for adiabatic process). Is this equation wrong? Forgive my questioning, but I am trying to understand the why. I don't want to simply plod through the mechanics of the math.

(Looking at it from a strict definition standpoint it makes sense - for an adiabatic process - internal energy changes as much as work done, but since the work done come from the gas itself, the value changes!)
 
chopnhack said:
Ok, I see the manipulation, simply restating the Q=U+W equation, solve for U instead. What would lead me to do that though? The lecture notes showed us many derivations and the one that came to mind when solving this problem was dU = dW = Cv×dT (for adiabatic process). Is this equation wrong? Forgive my questioning, but I am trying to understand the why. I don't want to simply plod through the mechanics of the math.
There are two sign conventions used in the literature for the first law: $$\Delta U=Q-W$$where W is the work done by the system on the surroundings, and $$\Delta U=Q+W$$whereW is the work done by the surroundings on the system? Which sign convention are you using?
 
  • Like
Likes   Reactions: chopnhack
Chestermiller said:
There are two sign conventions used in the literature for the first law: $$\Delta U=Q-W$$where W is the work done by the system on the surroundings, and $$\Delta U=Q+W$$whereW is the work done by the surroundings on the system? Which sign convention are you using?
Can we use dW = -dU?

Process 1: Adiabatic

dQ = 0 No heat added in an Adiabatic expansion, the gas expands using internal energy.

dW = -Cv×dT = 12.471 JK-1 × (389K-588K) à +2,482 J

dU = -dW = -2,482 J
 
  • #10
chopnhack said:
Can we use dW = -dU
Only if Q = 0. Otherwise $$\Delta U=Q-W$$and$$W=Q-\Delta U$$

(Please don't use d's when you mean ##\Delta##'s or, in the case of path-dependent quantities like heat and work, capitalized symbols Q and W).
 
  • Like
Likes   Reactions: chopnhack
  • #11
Chestermiller said:
Only if Q = 0. Otherwise $$\Delta U=Q-W$$and$$W=Q-\Delta U$$

(Please don't use d's when you mean ##\Delta##'s or, in the case of path-dependent quantities like heat and work, capitalized symbols Q and W).
Got it! only for adiabatic. Sorry, I was using what the professor taught us. He did mention not to call it 'd' but delta. Maybe he had a hard time with his software ;-)
Thank you for helping me understand this better. I was having fits with it!
 

Similar threads

  • · Replies 2 ·
Replies
2
Views
3K
Replies
8
Views
2K
  • · Replies 4 ·
Replies
4
Views
2K
  • · Replies 2 ·
Replies
2
Views
2K
Replies
16
Views
4K
  • · Replies 12 ·
Replies
12
Views
7K
  • · Replies 7 ·
Replies
7
Views
3K
Replies
2
Views
1K
  • · Replies 8 ·
Replies
8
Views
2K
  • · Replies 4 ·
Replies
4
Views
3K