Calculating Thermodynamic Heat and Work

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Discussion Overview

The discussion revolves around the calculation of thermodynamic heat and work for an ideal gas undergoing isothermal expansion against a constant pressure. Participants explore the implications of the first law of thermodynamics and the relationships between heat, work, and internal energy in this context.

Discussion Character

  • Homework-related
  • Technical explanation
  • Conceptual clarification
  • Debate/contested

Main Points Raised

  • One participant presents a problem involving the isothermal expansion of one mole of ideal gas and attempts to calculate work using the integral of pressure over volume.
  • Another participant suggests that the change in internal energy, ΔE, for an ideal gas in an isothermal process is zero.
  • Some participants propose that since ΔE is zero, the heat q must equal the negative of work w, implying a relationship between heat and work in this scenario.
  • There is a discussion about the validity of two different equations for calculating work, leading to different results, which raises questions about the applicability of each equation in this context.
  • One participant challenges the scenario by stating that an ideal gas cannot expand if both temperature and pressure are held constant, suggesting a fundamental issue with the problem setup.
  • Another participant explains the derivation of the second work equation from the first, noting its relevance to isothermal processes for ideal gases.

Areas of Agreement / Disagreement

Participants generally agree on the zero change in internal energy for an isothermal process, but there is disagreement regarding the applicability of the equations for work and the feasibility of the described scenario.

Contextual Notes

The discussion highlights potential limitations in the problem setup, particularly regarding the assumptions of constant temperature and pressure during the gas expansion, which may not be physically realizable.

Youngster
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Homework Statement



One mole of ideal gas expands isothermally at 20°C against a constant pressure of 1 atm from 20 to 30L. (1 atm = 1.013 x 105Pa; 1 m3 = 1000L

Find q, w, ΔE, and ΔH in Joules

Homework Equations



ΔE = q + w
w = -\intPdV
H = E + PV

The Attempt at a Solution



I solved for work using the second equation listed above. Since pressure is constant, I removed it from the integral and simply integrated the volume from 20L to 30L. This resulted in -10 atm x L.

Converting that to Joules using the conversion factors given, I obtained -1013 J as the thermodynamic work.

But then how do I obtain the thermodynamic heat?
 
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You need to figure out the change in the internal energy of the gas, ##\Delta E##, considering it is ideal.
 
Okay, so what I'm getting is that since it's an isothermal process, the change in internal energy is 0.

That would mean q is just the reverse of w. Does this sound right? That would mean this is reversible too, yes?
 
Youngster said:
Okay, so what I'm getting is that since it's an isothermal process, the change in internal energy is 0.

That would mean q is just the reverse of w. Does this sound right?
Yes. Just to be clear, the energy lost by the gas as it does work is compensated by heat coming in from the environment.

Youngster said:
That would mean this is reversible too, yes?
I guess that it is reasonable to assume that this is the result of a slow (quasistatic) process, for the temperature to be maintained constant during the entire process, and therefore it is reversible.
 
Ah yes, thank you.

I have one more item I'd like to clarify.

I have two equation for thermodynamic work listed in my notes.

1. w = -∫PdV
2. w = -nRT ln\frac{V_{2}}{V_{2}}

I used the first equation to obtain -1013J, but the second equation provides a different value of -987.7J. This is a pretty significant difference, so I'm curious what the differences between the equations are, if any.
 
I didn't pay enough attention to the original statement. The situation described is simply impossible: an ideal gas cannot expand when both temperature and pressure are held constant. Obviously, since ##PV = nR T##, ##V## can't change if ##P##, ##T##, and ##n## are all kept constant.

Otherwise, you get equation 2 from equation 1 by replacing ##P## by ##n R T/V##, and then integrating over ##V## for ##T## constant. Equation 2 is therefore useful for isothermal processes (for an ideal gas only).
 

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