Surface tension: Difference between revisions
Jump to navigation
Jump to search
mNo edit summary |
|||
Line 21: | Line 21: | ||
=== 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: | ||
Line 35: | Line 35: | ||
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;