How Does the Van der Waals Equation Define Adiabatic Processes for Real Gases?

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SUMMARY

The discussion focuses on the application of the van der Waals equation, specifically the equation \(\left(P+\frac{a}{v^2}\right)(v-b)=RT\), to derive the relationship for adiabatic processes in real gases. The key conclusion is that for a gas with a temperature-dependent heat capacity \(c_v\), the adiabatic process can be expressed as \(T(v-b)^{R/c_v}=constant\). This indicates that while the heat capacity for ideal gases is constant, the heat capacity for van der Waals gases varies with temperature but aligns with the ideal gas heat capacity in certain conditions. Understanding this relationship is crucial for engineers and physicists when analyzing real gas behavior.

PREREQUISITES
  • Understanding of the van der Waals equation for real gases
  • Knowledge of thermodynamic concepts, particularly adiabatic processes
  • Familiarity with heat capacity definitions and their implications
  • Basic calculus for integration and differential equations
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  • Study the derivation of the van der Waals equation and its implications for real gases
  • Learn about the relationship between heat capacity and temperature for real gases
  • Explore the differences between ideal and real gas behavior in thermodynamics
  • Investigate the applications of the van der Waals equation in engineering scenarios
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Students and professionals in thermodynamics, chemical engineering, and physics who are analyzing the behavior of real gases and their adiabatic processes.

arpon
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Homework Statement


Show that for a gas obeying the van der Waals equation ##\left(P+\frac{a}{v^2}\right)(v-b)=RT##, with ##c_v## a function of ##T## only, an equation for an adiabatic process is $$T(v-b)^{R/c_v}=constant$$

Homework Equations


##TdS=c_vdT+T\left(\frac{\partial P}{\partial T}\right)_v dv##

The Attempt at a Solution


For reversible adiabatic process, ##dS=0##.
So, from the third ##TdS## equation,
$$c_vdT+T\left(\frac{\partial P}{\partial T}\right)_v dv=0$$
$$c_vdT+T\left(\frac{R}{v-b}\right)dv=0~~~$$ [Using equation of state]
$$c_v\frac{dT}{T}=-\frac{RdV}{v-b}$$
If ##c_v## is a constant, integrating both sides, we have:
$$T(v-b)^{R/c_v}=constant$$
But, in this case, ##c_v## is a function of ##T##.
Any help would be appreciated.
 
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I guess they must be assuming that, over the range of temperatures for the process, the heat capacity is nearly constant. We certainly often do this for an ideal gas, and, since the heat capacity for a van der waals gas is a function only of temperature, it must be identical to the ideal gas heat capacity.
 
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Chestermiller said:
since the heat capacity for a van der waals gas is a function only of temperature, it must be identical to the ideal gas heat capacity
Could you please explain this part? The heat capacity for ideal gas is a constant while for van der waals gas, it is a function of temperature. What did you actually mean by they are identical?
 
arpon said:
Could you please explain this part? The heat capacity for ideal gas is a constant while for van der waals gas, it is a function of temperature. What did you actually mean by they are identical?
The heat capacity of a real gas, in the limit of very low pressures, is a function of temperature. We engineers take this into account in our definition of an ideal gas (by regarding an ideal gas as having a temperature-dependent heat capacity), but physicists have idealized it further (by regarding an ideal gas as having a constant heat capacity). Now, if the heat capacity of a van der Waals gas is a function of temperature only (and not volume and pressure), it must be the same temperature-dependent function as we engineers refer to for an ideal gas.
 
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