Chemical potential: Difference between revisions
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identical particles | identical particles | ||
:<math>Z_N= \left( \frac{2\pi m k_BT}{h^2} \right)^{3N/2} Q_N</math> | :<math>Z_N= \left( \frac{2\pi m k_BT}{h^2} \right)^{3N/2} Q_N</math> | ||
and <math>Q_N</math> is the [ | and <math>Q_N</math> is the | ||
[http://clesm.mae.ufl.edu/wiki.pub/index.php/Configuration_integral_%28statistical_mechanics%29 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== | ==Kirkwood charging formula== | ||
See Ref. 2 | See Ref. 2 |
Revision as of 18:27, 16 January 2008
Classical thermodynamics
Definition:
where is the Gibbs energy function, leading to
where is the Helmholtz energy function, is the Boltzmann constant, is the pressure, is the temperature and is the volume.
Statistical mechanics
The chemical potential is the derivative of the Helmholtz energy function with respect to the number of particles
where is the partition function for a fluid of identical particles
and is the configurational integral
Kirkwood charging formula
See Ref. 2
where is the intermolecular pair potential and is the pair correlation function.
See also
References
- T. A. Kaplan "The Chemical Potential", Journal of Statistical Physics 122 pp. 1237-1260 (2006)
- John G. Kirkwood "Statistical Mechanics of Fluid Mixtures", Journal of Chemical Physics 3 pp. 300-313 (1935)
- G. Cook and R. H. Dickerson "Understanding the chemical potential", American Journal of Physics 63 pp. 737-742 (1995)