Finding the entropy from the heat capacity

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SUMMARY

The discussion focuses on deriving entropy from heat capacity in a canonical ensemble, specifically using the equation for heat capacity, ##C_{V}=\alpha(N,V) T^{n}##. It establishes that entropy can be expressed as ##S(V,T)=\frac{1}{n} \alpha(N,V) T^{n} + f(N,V)##, where ##f(N,V)## accounts for additional terms lost in differentiation. The conversation highlights that while this method works under certain conditions, such as knowing ##S(V,0)=0##, it fails for ideal gases and requires consideration of phase changes in real substances.

PREREQUISITES
  • Understanding of canonical ensembles in statistical mechanics
  • Familiarity with heat capacity equations, specifically ##C_{V}##
  • Knowledge of entropy and its mathematical representation
  • Concept of phase changes in thermodynamics
NEXT STEPS
  • Study the derivation of entropy from heat capacity in various thermodynamic systems
  • Explore the implications of phase transitions on entropy calculations
  • Investigate the behavior of heat capacity for ideal gases and its limitations
  • Learn about the mathematical techniques for integrating complex functions in thermodynamics
USEFUL FOR

This discussion is beneficial for physicists, thermodynamicists, and students studying statistical mechanics, particularly those interested in the relationship between heat capacity and entropy in various substances.

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Let's say that we have some canonical ensemble where I know that the heat capacity is given by

##C_{V}=\alpha(N,V) T^{n}##

Since ##C_{V}=T\frac{\partial S(T,V)}{\partial T}## I know that

##S(V,T)=\frac{1}{n} \alpha(N,V) T^{n} + f(N,V) ##

Where the function ##f(N,V)## has to do with the fact that I'm only taking the derivative wrt. to T and can lose such additional terms in general.

I also know that ##S(V,0)=0## which means that ##f(N,V,)=0## which means I can always use this trick to find the entropy if the heat capacity is known. Obviously if ##C_{V}## is an uglier function of T we'd have to integrate and so on.

##QUESTION##: When is it okay to do such a reasoning and when isn't it?
 
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For an ideal gas, assuming CV is constant, ##S = N(C_vln(T) + R ln(V)+C)##. So this doesn't even work for an ideal gas. For real substances, there are phase changes that occur prior to getting to absolute zero that need to be included also.
 

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