Entropy change in a irreversible adiabatic process

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Discussion Overview

The discussion revolves around the entropy change in an irreversible adiabatic process involving an ideal monatomic gas. Participants explore the implications of adiabatic conditions, the definition of reversible versus irreversible processes, and the calculation of entropy changes in such scenarios.

Discussion Character

  • Exploratory
  • Technical explanation
  • Conceptual clarification
  • Debate/contested

Main Points Raised

  • Some participants assert that in adiabatic processes, q = 0, leading to questions about whether dS can be zero.
  • Others clarify that dS is not zero in all adiabatic processes and that dS = dq/T applies only to reversible processes.
  • One participant proposes a reversible isothermal expansion as a potential reversible path to calculate entropy change.
  • Another participant agrees with the proposed reversible isothermal expansion, indicating it aligns with their thoughts.
  • There is a question about the nature of reversible and irreversible processes, specifically regarding the possibility of a reversible adiabatic path being equivalent to the irreversible one.
  • Participants discuss the necessity of maintaining constant temperature in reversible processes and the implications of doing work against a vacuum in the context of the problem.
  • Clarifications are made regarding the differences between isothermal and adiabatic paths on a p-v diagram, emphasizing that they are not the same line.

Areas of Agreement / Disagreement

Participants generally agree on the distinction between reversible and irreversible processes, but multiple competing views remain regarding the specifics of entropy change calculations and the nature of the paths involved.

Contextual Notes

Limitations include the assumptions made about the ideal gas behavior, the definitions of reversible and irreversible processes, and the specific conditions under which temperature and pressure are controlled.

chemkid01
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One mole of an ideal monatomic gas initially at 298 k expands from 1.0 L to 10.0 L. Assume the expansion is irreversible, adiabatic, and no work is done. Calculate delta S of the gas and delta S of the surroundings.

I know that delta dS = dq/T but q = 0 in adiabatic processes right? So does dS = 0 in all adiabatic processes?
 
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chemkid01 said:
One mole of an ideal monatomic gas initially at 298 k expands from 1.0 L to 10.0 L. Assume the expansion is irreversible, adiabatic, and no work is done. Calculate delta S of the gas and delta S of the surroundings.

I know that delta dS = dq/T but q = 0 in adiabatic processes right? So does dS = 0 in all adiabatic processes?
Hi chemkid01. Welcome to Physics Forums!

dS is not equal to zero in all adiabatic processes, and dS is not equal to dq/T, except in reversible processes. Your process is not a reversible process. To figure out what the entropy change is for an irreversible process, you need to dream up a reversible path between the exact same initial equilibrium state of the system and the exact same final equilibrium state. For that path, dS = dq/T, and you can get the entropy change. For more details on this, see my Blog at my PF home page.
 
Ok, so for this case, since the process is adiabatic and q = 0 and no work is done, then delta U = q + w = 0. And since it's an ideal gas, U only depends on T so T is constant as well. So could my dreamed up reversible process be a reversible isothermal expansion from 1.0 L to 10.0 L at 298 k?
 
chemkid01 said:
Ok, so for this case, since the process is adiabatic and q = 0 and no work is done, then delta U = q + w = 0. And since it's an ideal gas, U only depends on T so T is constant as well. So could my dreamed up reversible process be a reversible isothermal expansion from 1.0 L to 10.0 L at 298 k?
Yes. Nice analysis. That's the one I was thinking of.

Chet
 
Ok, thanks for the help! One more thing, I'm not exactly sure what makes a process reversible/irreversible. For example, the question says that it is an irreversible, adiabatic expansion from 1.0 L to 10.0 L. Why can't my alternate reversible path simply be a reversible, adiabatic expansion from 1.0 L to 10.0 L. Is that possible?
 
chemkid01 said:
Ok, thanks for the help! One more thing, I'm not exactly sure what makes a process reversible/irreversible. For example, the question says that it is an irreversible, adiabatic expansion from 1.0 L to 10.0 L. Why can't my alternate reversible path simply be a reversible, adiabatic expansion from 1.0 L to 10.0 L. Is that possible?
No, because you won't be able to hold the temperature constant over that reversible path. So, the initial and final equilibrium states won't be the same as for the original irreversible path.

Chet
 
Hmm, ok, I don't think I quite understand reversibility. Could you explain what it is about the path being reversible that makes it so you won't be able to hold the temperature constant? Also, on a side note, since a reversible, isothermal expansion does bring you from the same initial state to the same final state as the irreversible, adiabatic expansion, does that mean that in this case, on the p-v diagram, the isotherm and the adiabat are the same line? Thanks a lot for your help by the way!
 
chemkid01 said:
Hmm, ok, I don't think I quite understand reversibility.

Again, I refer you to my Blog. If a process is carried out irreversibly, the temperature and/or the pressure will vary with spatial position within the system. To go from the initial state to the final state reversibly, you need to control the temperature and the pressure at the interface with the surroundings such that the variations of temperature and pressure within the system are vanishingly small. This can be done by changing the temperature and pressure at the interface very gradually, so the system has time to respond, and such that, at any instant of time during the transition, the system is only vanishingly removed from thermodynamic equilibirum.
Could you explain what it is about the path being reversible that makes it so you won't be able to hold the temperature constant?
In the case you are studying, no work is being done by the expanding gas, because the gas is essentially expanding against a vacuum. To carry out the process reversibly (and isothermally), you need to provide a force against the expansion, and very gradually back off on this force. This allows the system to do work against the force. To hold the temperature constant during this reversible path, you need to add heat Q. If you try to do it adiabatically, ΔU=-W, and the temperature will drop. So the reversible path between the initial and final states (which, for your problem are at the same temperature) can't be accomplished unless you add heat.

Also, on a side note, since a reversible, isothermal expansion does bring you from the same initial state to the same final state as the irreversible, adiabatic expansion, does that mean that in this case, on the p-v diagram, the isotherm and the adiabat are the same line?

No. The reversible path between the initial and final states is not adiabatic.

Chet
 

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