A simple kinetic model for the phase transition of the van der Waals fluid
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Abstract: A simple kinetic model, which is presumably minimum, for the phase transition of the van der Waals fluid is presented. In the model, intermolecular collisions for a dense gas has not been treated faithfully. Instead, the expected interactions as the non-ideal gas effect are confined in a self-consistent force term. Collision term plays just a role of thermal bath. Accordingly, it conserves neither momentum nor energy, even globally. It is demonstrated that (i) by a natural separation of the mean-field self-consistent potential, the potential for the non-ideal gas effect is determined from the equation of state for the van der Waals fluid, with the aid of the balance equation of momentum, (ii) a functional which monotonically decreases in time is identified by the H theorem and is found to have a close relation to the Helmholtz free energy in thermodynamics, and (iii) the Cahn--Hilliard type equation is obtained in the continuum limit of the present kinetic model. Numerical simulations based on the Cahn--Hilliard type equation are also performed.
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- Mean field kinetic theory description of evaporation of a fluid into vacuum
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(8)- Vapor-liquid phase transition: The van der Waals model
- Degenerate Cahn-Hilliard equation: from nonlocal to local
- Molecular kinetic modelling of non-equilibrium transport of confined van der Waals fluids
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