Chemical potential: Difference between revisions

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where <math>G</math> is the [[Gibbs energy function]], leading to  
where <math>G</math> is the [[Gibbs energy function]], leading to  


:<math>\mu=\frac{A}{Nk_B T} + \frac{pV}{Nk_BT}</math>
:<math>\frac{\mu}{k_B T}=\frac{G}{N k_B T}=\frac{A}{N k_B T}+\frac{p V}{N k_B T}</math>


where <math>A</math> is the [[Helmholtz energy function]], <math>k_B</math>
where <math>A</math> is the [[Helmholtz energy function]], <math>k_B</math>

Revision as of 15:39, 18 August 2014

Classical thermodynamics

Definition:

μ=∂G∂N|T,p=∂A∂N|T,V

where G is the Gibbs energy function, leading to

μkBT=GNkBT=ANkBT+pVNkBT

where A is the Helmholtz energy function, kB is the Boltzmann constant, p is the pressure, T is the temperature and V is the volume.

Statistical mechanics

The chemical potential is the derivative of the Helmholtz energy function with respect to the number of particles

μ=∂A∂N|T,V=∂(−kBTlnZN)∂N=−kBT[32ln(2πmkBTh2)+∂lnQN∂N]

where ZN is the partition function for a fluid of N identical particles

ZN=(2πmkBTh2)3N/2QN

and QN is the configurational integral

QN=1N!∫...∫exp(−UN/kBT)dr1...drN

Kirkwood charging formula

The Kirkwood charging formula is given by [1]

βμex=ρ∫01dλ∫∂βΦ12(r,λ)∂λg(r,λ)dr

where Φ12(r) is the intermolecular pair potential and g(r) is the pair correlation function.

See also

References

Related reading