Chemical potential: Difference between revisions

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Definition:
Definition:


:<math>\mu=\frac{\partial G}{\partial N}</math>
:<math>\mu=\left. \frac{\partial G}{\partial N}\right\vert_{T,p}</math>


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


:<math>\mu= \frac{\partial A}{\partial N}=\frac{\partial (-k_B T \ln Z_N)}{\partial N} = -\frac{3}{2} k_BT \ln \left(\frac{2\pi m k_BT}{h^2}\right) + \frac{\partial \ln Q_N}{\partial N}</math>
:<math>\mu= \left. \frac{\partial A}{\partial N}\right\vert_{T,V}=\frac{\partial (-k_B T \ln Z_N)}{\partial N} = -\frac{3}{2} k_BT \ln \left(\frac{2\pi m k_BT}{h^2}\right) + \frac{\partial \ln Q_N}{\partial N}</math>
where <math>Z_N</math> is the [[partition function]] for a fluid of <math>N</math>
where <math>Z_N</math> is the [[partition function]] for a fluid of <math>N</math>
identical particles
identical particles

Revision as of 15:42, 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