Van der Waal expansion and delivered work

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SUMMARY

The discussion focuses on the isothermal expansion of one mole of an ideal van der Waals fluid, utilizing the equation dW_{RWS} = (1 - T_{RHS}/T)(-dQ) + (-dW) to calculate work delivered to a reversible work source (RWS). The key equations include the van der Waals equations for pressure and entropy, which are essential for understanding the energy and entropy conservation principles involved. The participant successfully integrates the equations but identifies a critical error regarding the ratio T_c/T_h, indicating a misunderstanding of the heat sources involved. Clarification is sought on the correct interpretation of the heat terms in the equations.

PREREQUISITES
  • Understanding of van der Waals equations and their application in thermodynamics.
  • Familiarity with concepts of isothermal processes and reversible work sources.
  • Knowledge of energy and entropy conservation laws in thermodynamic systems.
  • Ability to perform integration of thermodynamic equations.
NEXT STEPS
  • Study the derivation and implications of the van der Waals equation for real gases.
  • Learn about the principles of reversible and irreversible thermodynamic processes.
  • Explore the concept of heat transfer in thermodynamic systems, focusing on the role of thermal reservoirs.
  • Investigate common pitfalls in thermodynamic calculations, particularly regarding energy and entropy conservation.
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Students and professionals in thermodynamics, particularly those studying or working with ideal and real gas behaviors, as well as researchers focusing on energy transfer and conservation in thermodynamic systems.

Dazed&Confused
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Homework Statement


Assume that one mole of an ideal van der Waals fluid is expanded isothermally, at temperature T_h from an initial volume V_i to a final volume V_f. A thermal reselvoir at temperature T_c is available. Apply <br /> dW_{RWS} = \left ( 1 - \frac{T_{RHS}}{T} \right ) (-dQ) +(-dW)
to a differential process and integrate to calculate the work delivered to a reversible work source (RWS). RHS is reversible heat source. Corroborate by overall energy and entropy conservation.

Hint: remember to add the direct work transfer pdV to obtain the total work delivered to the reversible work source.

Homework Equations


Van der Waal equations:
<br /> u + a/v = cRT<br />
where u, a, v, c, R, T are, respectively, energy per mole, constant, volume per mole, another constant, temperature.
<br /> p = \frac{RT}{v-b} - \frac{a}{v^2}<br />

The entropy is
<br /> S = NR\log [ (v-b)(cRT)^c] + Ns_0<br />
where N is the number of moles and b is another constant.

The Attempt at a Solution


[/B]
Using the first equation with T=T_h, T_{RHS} = T_c and -dW = pdV and integrating we get
<br /> W_{RHS} = - \left ( 1- \frac{T_c}{T_h} \right) Q + RT_h \log \left ( \frac{v_f-b}{v_i - b} \right) + \frac{a}{v_f} - \frac{a}{v_i}<br />
Also energy conservation gives
<br /> \Delta u + W + Q =0<br />
and entropy conservation
R \log \left ( \frac{v_f-b}{v_i - b} \right) + \frac{Q}{T_c} = 0<br />
Finally the energy change is
<br /> \Delta u = \frac{a}{v_i} - \frac{a}{v_f}<br />
Everything seems to work out except that fraction T_c/T_h is the wrong way round and I see no way of dealing with this. Help would be appreciated.
 
Last edited:
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I see my problem: there are two Qs. The first equation was the heat from the subsystem and the energy and entropy the heat RHS.
 

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