Q and W for Van-der-Waals Gases

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SUMMARY

This discussion focuses on calculating heat (Q) and work (W) for Van-der-Waals gases, specifically addressing the relationship between internal energy change (ΔU), heat, and work. The equation ΔU = Q + W is confirmed, with the participant calculating ΔU as 104.98 J and Q as 7502.55 J based on integration results from Wolfram Alpha. The conversation emphasizes the importance of understanding the differences between ideal gases and Van-der-Waals gases in thermodynamic calculations.

PREREQUISITES
  • Understanding of the first law of thermodynamics (ΔU = Q + W)
  • Familiarity with Van-der-Waals gas equations
  • Basic knowledge of integration techniques in thermodynamics
  • Experience with using computational tools like Wolfram Alpha for verification
NEXT STEPS
  • Study the Van-der-Waals equation and its implications for real gases
  • Learn about the integration of thermodynamic equations for work done in quasi-static processes
  • Explore the differences between ideal gas behavior and real gas behavior
  • Investigate the use of computational tools for thermodynamic calculations
USEFUL FOR

Students and professionals in thermodynamics, particularly those studying real gas behavior, as well as anyone involved in calculating thermodynamic properties of gases.

krootox217
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Homework Statement


I have the following task:

43921_1.PNG


Homework Equations

The Attempt at a Solution



I already managed to calculate Delta Um, but how do I calculate Q und W. Can I use the equations for the isothermic expansion for ideal gases, even if this are Van-der-Waals Gases?
 
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Hello. Welcome to PF!

What is the most basic formula you know for calculating the work done by a system for any quasi-static process? Hint: This formula was probably presented when you first introduced the concept of work in thermodynamics.
 
e701045752be3b1a02f4255078f9754e.png

This one?
 
krootox217 said:
e701045752be3b1a02f4255078f9754e.png

This one?
Yes. They obviously want you to assume that the expansion is reversible. Your equation is correct if W represents the work done by the surroundings on the system.

Chet
 
Ok, thanks a lot!

therefore, Q = -W?
 
krootox217 said:
Ok, thanks a lot!

therefore, Q = -W?
No. ΔUm is not equal to zero.

Chet
 
krootox217 said:
This means, that delta U = Q + W and I have to subtract the Work from Delta U?I have another Question, the integral is according to Wolfram alpha -7397.55 J

http://www.wolframalpha.com/input/?i=-+integral+from+0.001+to+0.020+((8.314*298.15)/(V-(3.2*10^-5))-(0.1105)/(V^2))+dV

And I calculated a Delta U of 104.98J

Therefore my Q is 7502.55J

Are these values posible?
You don't need to ask me this. Why don't you solve the same the same problem using the ideal gas law and see how the numbers compare? Incidentally, why did you need wolframalpha to do the integration for you? Why didn't you do the integration yourself?

Chet
 
I calculated it by myself, but I often use wolfram alpha to check my results, and in this case, the result was the same, so it was easier just to paste the wolfram alpha link :)

Well, since delta U should be =0 for ideal gases, this small change seems possible?
 
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  • #10
krootox217 said:
I calculated it by myself, but I often use wolfram alpha to check my results, and in this case, the result was the same, so it was easier just to paste the wolfram alpha link :)

Well, since delta U should be =0 for ideal gases, this small change seems possible?
Sure. Wouldn't you have expected that?

Chet
 
Last edited:
  • #11
I wasn't sure,

but now it makes sense.

Thanks a lot!
 

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