Chemical potential: Difference between revisions

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and <math>Q_N</math> is the [[configurational integral]]
and <math>Q_N</math> is the [[configurational integral]]
:<math>Q_N = \frac{1}{N!} \int ... \int \exp (-U_N/k_B T) dr_1...dr_N</math>
:<math>Q_N = \frac{1}{N!} \int ... \int \exp (-U_N/k_B T) dr_1...dr_N</math>
==Kirkwood charging formula==
See Ref. 2
:<math>\beta \mu_{\rm ex} = \rho \int_0^1 d\lambda \int \frac{\partial \beta \Phi_{12} (r,\lambda)}{\partial \lambda} {\rm g}(r,\lambda) dr</math>
where <math>\Phi_{12}(r)</math> is the [[intermolecular pair potential]] and <math>{\rm g}(r)</math> is the [[Pair distribution function | pair correlation function]].
==See also==
==See also==
*[[Ideal gas: Chemical potential]]
*[[Ideal gas: Chemical potential]]
==References==
==References==
#[http://dx.doi.org/10.1007/s10955-005-8067-x T. A. Kaplan "The Chemical Potential", Journal of Statistical Physics '''122''' pp. 1237-1260 (2006)]
#[http://dx.doi.org/10.1007/s10955-005-8067-x T. A. Kaplan "The Chemical Potential", Journal of Statistical Physics '''122''' pp. 1237-1260 (2006)]
#[http://dx.doi.org/10.1063/1.1749657  John G. Kirkwood "Statistical Mechanics of Fluid Mixtures", Journal of Chemical Physics '''3''' pp. 300-313 (1935)]
[[category:classical thermodynamics]]
[[category:classical thermodynamics]]
[[category:statistical mechanics]]
[[category:statistical mechanics]]

Revision as of 09:41, 8 June 2007

Classical thermodynamics

Definition:

μ=∂G∂N|T,p

where G is the Gibbs energy function, leading to

μ=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=−32kBTln(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

See Ref. 2

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

  1. T. A. Kaplan "The Chemical Potential", Journal of Statistical Physics 122 pp. 1237-1260 (2006)
  2. John G. Kirkwood "Statistical Mechanics of Fluid Mixtures", Journal of Chemical Physics 3 pp. 300-313 (1935)