Chemical potential: Difference between revisions

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:<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>
==See also==
==See also==
*[[Ideal gas chemical potential]]
*[[Ideal gas: Chemical potential]]

Revision as of 15:43, 22 May 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

See also