Surface tension: Difference between revisions
		
		
		
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| === Binder procedure=== | |||
| For given conditions of volume and temperature, the [[Helmholtz  energy function]] is computed as a function of the number of molecules: | For given conditions of volume and temperature, the [[Helmholtz  energy function]] is computed as a function of the number of molecules: | ||
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| to compute the densities of the two phases; <math> \rho_v, \rho_l </math>   | to compute the densities of the two phases; <math> \rho_v, \rho_l </math>   | ||
| === Explicit interfaces === | |||
| == Mixtures == | == Mixtures == | ||
Revision as of 11:06, 1 August 2007
The surface tension, , is a measure of the work required to create a surface.
Thermodynamics
In the Canonical ensemble: two phases;
- ;
where
- is the number of particles
- is the volume
- is the temperature
- is the surface area
- is the Helmholtz energy function
Computer Simulation
A review on different techniques to compute surface (interface) tension can be found in the paper by Gloor et al.
Liquid-Vapour Interfaces of one component systems
Binder procedure
For given conditions of volume and temperature, the Helmholtz energy function is computed as a function of the number of molecules:
The calculation is usually carried out using Monte Carlo simulation
If liquid-vapour equilibrium occurs, the plot of the chemical potential, , as a function of shows a loop.
Using basic thermodynamic procedures (Maxwell construction) it is possible to compute the densities of the two phases;