LAUSR

The molecular interactions of numerous real fluids, like argon, nitrogen, or carbon dioxide, are adequately described by the two-center Lennard-Jones plus quadrupole potential. Applying this model class in molecular dynamics simulations, evaporation is investigated systematically. The influence of the molecular anisotropy and quadrupole as well as the boundary conditions, i.e., bulk liquid temperature and evaporation magnitude, is reported. A method for specifying the evaporation magnitude in terms of hydrodynamic velocity is further developed for that purpose. Analyses show that the largest molar flux and energy flux occur for spherical molecules and that anisotropy and quadrupole influence several quantities. Depending on the bulk liquid temperature, the quadrupole predominantly affects the interface temperature, while the anisotropy of the molecule significantly influences the interface temperature as well as both molar and energy fluxes. In addition, the preferred average orientation of the molecules in the interface region is investigated. The evaporation coefficient is determined, and thermodynamic states traversed during the evaporation process are discussed.