Calculating Work in Isothermal Processes of Carnot Cycle

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Discussion Overview

The discussion revolves around calculating the work done in the isothermal processes of the Carnot cycle, specifically focusing on the relationships between volumes during these processes. Participants explore the equations for work in isothermal conditions and the implications of the first law of thermodynamics in the context of the Carnot cycle.

Discussion Character

  • Technical explanation
  • Mathematical reasoning
  • Debate/contested

Main Points Raised

  • Abbigale questions the equality of volume ratios (\(\frac{V_{A}}{V_{\text{B}}} = \frac{V_{D}}{V_{C}}\)) in the context of calculating work done in isothermal processes.
  • Some participants suggest that the equality arises from the mathematical relationships derived from the first law of thermodynamics, where the work done in the cycle is equal to the heat transferred during isothermal processes.
  • Others propose that the relationship can be demonstrated using the PV diagram, contingent on the scale being shown.
  • AM introduces adiabatic equations for ideal gases and discusses how they relate to the isothermal processes, suggesting that the ratios of volumes can be derived from these equations.
  • There is mention of the need to be careful with the logic surrounding the definitions of thermodynamic temperature and its relationship to ideal gas behavior.

Areas of Agreement / Disagreement

Participants express differing views on the justification of the volume ratio equality, with some supporting it through thermodynamic principles while others seek visual or mathematical proofs. The discussion remains unresolved regarding the clarity of the relationship between the volumes.

Contextual Notes

Limitations include the dependence on ideal gas assumptions and the need for clarity in the definitions of temperature and volume ratios in the context of the Carnot cycle.

Abigale
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Hallo,

I read about thr Carnot-Cycle and got a problem.

A->B: isothermal
B->C: adiabatic
C->D: isothermal
D->A: adiabatic


I want to understand how to calculate the work done in the isothermal processes.
I have read:

[itex] W_{AB}= T_{H}Nk\ln{(\frac{V_{A}}{V_{\text{B}}})}\\<br /> <br /> W_{CD}= -T_{n}Nk\ln{(\frac{V_{A}}{V_{\text{B}}})}[/itex]

But if i callculate i get:
[itex] W_{CD}= -T_{n}Nk\ln{(\frac{V_{D}}{V_{C}})}[/itex]

So the question is, why is:
[itex] (\frac{V_{A}}{V_{\text{B}}}) = (\frac{V_{D}}{V_{C}})[/itex] ?

Thx
Abbigale :wink:
 
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Abigale said:
Hallo,

I read about thr Carnot-Cycle and got a problem.

A->B: isothermal
B->C: adiabatic
C->D: isothermal
D->A: adiabatic


I want to understand how to calculate the work done in the isothermal processes.
I have read:

[itex] W_{AB}= T_{H}Nk\ln{(\frac{V_{A}}{V_{\text{B}}})}\\<br /> <br /> W_{CD}= -T_{n}Nk\ln{(\frac{V_{A}}{V_{\text{B}}})}[/itex]

But if i callculate i get:
[itex] W_{CD}= -T_{n}Nk\ln{(\frac{V_{D}}{V_{C}})}[/itex]

So the question is, why is:
[itex] (\frac{V_{A}}{V_{\text{B}}}) = (\frac{V_{D}}{V_{C}})[/itex] ?
Abigale,

From the first law we know that ΔU + W = Q where W is the work done BY the gas. But since ΔU = 0 in one complete cycle, W = Q = heat flow in from hot register - heat flow out to cold register = |Qh| - |Qc|. Heat flow occurs only from A-B and C-D, so the difference in these heat flows is the work done for the entire cycle. That means the work done in the adiabatic parts nets out to 0.

The efficiency is:

[tex]\eta = 1 - \frac{|Q_c|}{|Q_h|} = 1 - \frac{T_cNk\ln\left(\frac{V_D}{V_C}\right)}{T_hNk\ln\left(\frac{V_A}{V_B}\right)}[/tex]

But we also know that for a Carnot cycle:

ΔS = Qh/Th + Qc/Th = 0 so |Qc/Qh| = Tc/Th

This necessarily means that [itex](\frac{V_{A}}{V_{\text{B}}}) = (\frac{V_{D}}{V_{C}})[/itex]

AM
 
Hey,
but is it possible to schow the Relation, just by looking at the pv-diagram?
 
Abigale said:
Hey,
but is it possible to show the Relation, just by looking at the pv-diagram?
Yes, if the PV graph showed the scale.

AM
 
The equations you give for isothermal work are for an ideal gas.

Since we're dealing with an ideal gas we can use the adiabatic equations for an ideal gas, for BC and DA.

So [itex]p_B V_B^{\gamma} = p_C V_C^{\gamma}[/itex]

and [itex]p_A V_A^{\gamma} = p_D V_D^{\gamma}[/itex]

dividing: [itex]\frac{p_B}{p_A} \frac{V_B^{\gamma}}{V_A^{\gamma}} = \frac{p_C}{p_D} \frac{V_C^{\gamma}} {V_D^{\gamma}}[/itex]

But for the isothermals: [itex]\frac{p_B}{p_A} = \frac{V_A}{V_B}[/itex] and [itex]\frac{p_C}{p_D} = \frac{V_D}{V_C}.[/itex]

We can now eliminate the pressure ratios from the previous equation, giving...

[itex]\frac{V_B^{\gamma - 1}}{V_A^{\gamma - 1}} = \frac{V_C^{\gamma - 1}} {V_D^{\gamma - 1}}[/itex]

So [itex]\frac{V_B}{V_A} = \frac{V_C} {V_D}[/itex]
 
Philip Wood said:
The equations you give for isothermal work are for an ideal gas.

Since we're dealing with an ideal gas we can use the adiabatic equations for an ideal gas, for BC and DA.

So [itex]p_B V_B^{\gamma} = p_C V_C^{\gamma}[/itex]

and [itex]p_A V_A^{\gamma} = p_D V_D^{\gamma}[/itex]

dividing: [itex]\frac{p_B}{p_A} \frac{V_B^{\gamma}}{V_A^{\gamma}} = \frac{p_C}{p_D} \frac{V_C^{\gamma}} {V_D^{\gamma}}[/itex]

But for the isothermals: [itex]\frac{p_B}{p_A} = \frac{V_A}{V_B}[/itex] and [itex]\frac{p_C}{p_D} = \frac{V_D}{V_C}.[/itex]

We can now eliminate the pressure ratios from the previous equation, giving...

[itex]\frac{V_B^{\gamma - 1}}{V_A^{\gamma - 1}} = \frac{V_C^{\gamma - 1}} {V_D^{\gamma - 1}}[/itex]

So [itex]\frac{V_B}{V_A} = \frac{V_C} {V_D}[/itex]
It might be easier to use the adiabatic condition in terms of temperature and volume:

[itex]TV^{\gamma - 1} = K[/itex] from which it is apparent that adiabatic paths between the same two temperatures result in the same proportional changes in volume.

AM
 
Much neater – if you can remember TVγ-1 = K. [Though, I suppose TVanything = K would suffice!]

We've got to be careful of the logic here. OP's argument leads to [itex]\left| \frac{Q_{AB}}{Q_{CD}} \right| = \frac{T_{AB}}{T_{CD}}[/itex]. The temperatures which appear in this equation are (in my interpretation of the above argument) ideal gas scale temperatures, effectively defined by pV = nRT. But the Second Law leads to a definition of thermodynamic temperature based on Carnot cycles for any working substance (not just an ideal gas) that is essentially [itex]\frac{T_{AB}}{T_{CD}} = \left| \frac{Q_{AB}}{Q_{CD}} \right|[/itex]. Hence the OP's argument shows the equivalence of the thermodynamic scale and the ideal gas scale.
 
Last edited:

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