Virial equation of state: Difference between revisions
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The [[second virial coefficient]] represents the initial departure from ideal-gas behavior | The [[second virial coefficient]] represents the initial departure from ideal-gas behavior | ||
:<math>B_{2}(T)= \frac{ | :<math>B_{2}(T)= \frac{N_A}{2V} \int .... \int (1-e^{-\Phi/k_BT}) ~d\tau_1 d\tau_2</math> | ||
where <math> | where <math>N_A</math> is [[Avogadro constant | Avogadros number]] and <math>d\tau_1</math> and <math>d\tau_2</math> are volume elements of two different molecules | ||
in configuration space. | in configuration space. | ||
Revision as of 13:54, 19 February 2008
The virial equation of state is used to describe the behavior of diluted gases. It is usually written as an expansion of the compressibility factor, , in terms of either the density or the pressure. Such an expansion was first introduced by Kammerlingh Onnes. In the first case:
- .
where
- is the pressure
- is the volume
- is the number of molecules
- is the (number) density
- is called the k-th virial coefficient
Virial coefficients
The second virial coefficient represents the initial departure from ideal-gas behavior
where is Avogadros number and and are volume elements of two different molecules in configuration space.
One can write the third virial coefficient as
where f is the Mayer f-function (see also: Cluster integrals). See also:
Convergence
See Ref. 3.
References
- H. Kammerlingh Onnes "", Communications from the Physical Laboratory Leiden 71 (1901)
- James A Beattie and Walter H Stockmayer "Equations of state", Reports on Progress in Physics 7 pp. 195-229 (1940)
- J. L. Lebowitz and O. Penrose "Convergence of Virial Expansions", Journal of Mathematical Physics 5 pp. 841-847 (1964)