Understanding Reversible Adiabatic Processes in Thermodynamics

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Homework Help Overview

The discussion revolves around reversible adiabatic processes in thermodynamics, specifically focusing on the ability to plot process paths in P-V-T coordinates and the implications of non-reversible processes. Participants explore the conditions under which the ideal gas law applies and the differences between reversible and non-reversible processes.

Discussion Character

  • Conceptual clarification, Assumption checking, Problem interpretation

Approaches and Questions Raised

  • Participants discuss the nature of reversible adiabatic processes and their equilibrium conditions, contrasting them with non-reversible processes. Questions arise regarding the applicability of the ideal gas law in different scenarios, particularly when systems are not in equilibrium.

Discussion Status

The discussion is active, with participants offering insights and questioning assumptions about equilibrium and the ideal gas law. Some participants express uncertainty about their understanding, while others provide examples to illustrate their points. There is no explicit consensus, but various interpretations and clarifications are being explored.

Contextual Notes

Participants are navigating the complexities of thermodynamic processes, particularly the definitions and conditions that govern reversible versus non-reversible adiabatic processes. The implications of sudden expansions and the concept of equilibrium are central to the discussion.

asdf1
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Why in a reversible adiabatic process you can plot the exact process path in the P-V-T coordinates, but you can't do so under different conditions?
 
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I'll take a stab at this although I'm not sure if I understand the question:

Could this be referring to the fact that an isothermal process must be performed "quasi-statically"? That is, to get close to isothermal, you would have to progress very slowly to allow for the system to canstantly return to equilibrium. The real isothermal process would appear to be a "staircase" that is overlaid on a perfect isotherm.

Stop me now if I'm on the wrong path. I could go on.
 
asdf1 said:
Why in a reversible adiabatic process you can plot the exact process path in the P-V-T coordinates, but you can't do so under different conditions?
I assume that "under different conditions" refers to a non-reversible adiabatic process. An example of such a process would be a sudden expansion of gas in an insulated container due to a sudden reduction of outside pressure. Such a process is generally thought to be adiabatic since there is no exchange of heat with the surroundings.

When this occurs, however, the system is not in equilibrium. So PV=nRT does not apply until the gas reaches equilibrium, which is after expansion has stopped and the translational kinetic energy of the gas has been converted to heat of the gas. Consequently, we cannot provide precise values for P, V and T during the process.

A reversible adiabatic process requires the system to be in equilibrium at all times during the process (an very slow expansion of gas in an insulated container). In such a process PV=nRT applies at all times so we can determine exactly what P, V and T will be at all times.

AM
 
I thought that PV=nRT is true no matter what for ideal gases. Why can't it be true if the system isn't in equilibrium?
 
asdf1 said:
I thought that PV=nRT is true no matter what for ideal gases. Why can't it be true if the system isn't in equilibrium?
PV=nRT is a relationship between P, V and T in a gas that is in equilibrium. Suppose you have a can of compressed air and open it up in outer space. [itex]P_0V_0 =nRT_0[/itex] = the energy of the compressed gas, and the gas does no work in a free expansion and no heat is exchanged with the surroundings. Does P'V' (pressure and volume at time t', say) represent the energy of the expanding gas? If so, it must be the same as the original energy: [itex]P'V' = P_0V_0 =nRT_0 = nRT'[/itex]. This would mean that the temperature is constant. Is that true? How do you define the temperature of an expanding gas? What about the translational kinetic energy of the gas molecules? Where does that fit into PV=nRT?

AM
 
Thank you! :)
 

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