Surface tension: Difference between revisions

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== Thermodynamics ==  
== Thermodynamics ==  
In the [[Canonical ensemble]]: two phases;
In the [[Canonical ensemble]] the surface tension is formally given as:


:<math> \gamma = \frac{ \partial A (N,V,T, {\mathcal A} )}{\partial  {\mathcal A} } </math>;
:<math> \gamma = \frac{ \partial A (N,V,T, {\mathcal A} )}{\partial  {\mathcal A} } </math>;
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*<math> {\mathcal A} </math> is the surface area
*<math> {\mathcal A} </math> is the surface area
*<math>A</math> is the [[Helmholtz energy function]]
*<math>A</math> is the [[Helmholtz energy function]]
==Computer Simulation==
==Computer Simulation==



Revision as of 12:09, 1 August 2007

The surface tension, γ, is a measure of the work required to create a surface.

Thermodynamics

In the Canonical ensemble the surface tension is formally given as:

γ=∂A(N,V,T,A)∂A;

where

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:

A(N;V,T)

The calculation is usually carried out using Monte Carlo simulation

If liquid-vapour equilibrium occurs, the plot of the chemical potential, μ≡(∂A/∂N)V,T, as a function of N shows a loop.

Using basic thermodynamic procedures (Maxwell construction) it is possible to compute the densities of the two phases; ρv,ρl

Explicit interfaces

Mixtures

References

category