Compressibility equation: Difference between revisions
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The '''compressibility equation''' (<math>\chi</math>) can be derived from the density fluctuations of the [[grand canonical ensemble]] (Eq. 3.16 | The '''compressibility equation''' (<math>\chi</math>) can be derived from the density fluctuations of the [[grand canonical ensemble]] (Eq. 3.16 in Ref. 1). For a homogeneous system: | ||
For a homogeneous system: | |||
:<math> | :<math>k_B T \left.\frac{\partial \rho }{\partial p}\right\vert_{T} = 1+ \rho \int h(r) ~{\rm d}{\mathbf r} = 1+\rho \int [{\rm g}^{(2)}({\mathbf r}) -1 ] {\rm d}{\mathbf r} | ||
= \frac{ \langle N^2 \rangle - \langle N\rangle^2}{\langle N\rangle}=\rho k_B T \chi_T</math> | |||
where <math>p</math> is the [[pressure]], <math>T</math> is the [[temperature]], <math>h</math> is the [[total correlation function]], <math>{\rm g}^{(2)}(r)</math> is the [[pair distribution function]] and <math>k_B</math> is the [[Boltzmann constant]]. | |||
For a spherical potential | For a spherical potential | ||
:<math>\frac{1}{ | :<math>\frac{1}{k_BT} \left.\frac{\partial p}{\partial \rho}\right\vert_{T} = 1 - \rho \int_0^{\infty} c(r) ~4 \pi r^2 ~{\rm d}r \equiv 1- \rho \hat{c}(0) | ||
\equiv \frac{1}{1+\rho \hat{h}(0)} \equiv \frac{1}{ 1 + \rho \int_0^{\infty} h(r) ~4 \pi r^2 ~{\rm d}r}</math> | \equiv \frac{1}{1+\rho \hat{h}(0)} \equiv \frac{1}{ 1 + \rho \int_0^{\infty} h(r) ~4 \pi r^2 ~{\rm d}r}</math> | ||
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is valid even when the inter-particle forces are not pairwise additive. | is valid even when the inter-particle forces are not pairwise additive. | ||
==References== | ==References== | ||
#[http://dx.doi.org/10.1088/0034-4885/28/1/306 J. S. Rowlinson "The equation of state of dense systems", Reports on Progress in Physics '''28''' pp. 169-199 (1965)] | |||
[[category: statistical mechanics]] |
Latest revision as of 18:24, 14 February 2008
The compressibility equation () can be derived from the density fluctuations of the grand canonical ensemble (Eq. 3.16 in Ref. 1). For a homogeneous system:
where is the pressure, is the temperature, is the total correlation function, is the pair distribution function and is the Boltzmann constant.
For a spherical potential
Note that the compressibility equation, unlike the energy and pressure equations, is valid even when the inter-particle forces are not pairwise additive.