Pressure equation: Difference between revisions
		
		
		
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| Carl McBride (talk | contribs) No edit summary | Carl McBride (talk | contribs)  m (Added internal link) | ||
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| :<math>p^*=\frac{\beta p}{\rho}= \frac{pV}{Nk_BT} = 1 - \beta \frac{2}{3} \pi  \rho \int_0^{\infty} \left( \frac{{\rm d}\Phi(r)} {{\rm d}r}~r \right)~{\rm g}(r)r^2~{\rm d}r</math> | :<math>p^*=\frac{\beta p}{\rho}= \frac{pV}{Nk_BT} = 1 - \beta \frac{2}{3} \pi  \rho \int_0^{\infty} \left( \frac{{\rm d}\Phi(r)} {{\rm d}r}~r \right)~{\rm g}(r)r^2~{\rm d}r</math> | ||
| where <math>\beta = 1/k_BT</math>, | where <math>\beta := 1/k_BT</math>, | ||
| <math>\Phi(r)</math> is a ''central'' [[Intermolecular pair potential | potential]] and <math>{\rm g}(r)</math> is the [[pair distribution function]]. | <math>\Phi(r)</math> is a ''central'' [[Intermolecular pair potential | potential]] and <math>{\rm g}(r)</math> is the [[pair distribution function]]. | ||
| ==See also== | |||
| *[[Virial pressure]] | |||
| ==References== | ==References== | ||
| [[category: statistical mechanics]] | [[category: statistical mechanics]] | ||
Revision as of 18:04, 27 February 2008
For particles acting through two-body central forces alone one may use the thermodynamic relation
Using this relation, along with the Helmholtz energy function and the canonical partition function, one arrives at the so-called pressure equation (also known as the virial equation):
where , is a central potential and is the pair distribution function.