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Thermodynamic and transport properties of simple fluids using lattice sums: bulk phases and liquid-vapour interface
Authors:J. LÓPEZ-LEMUS  J. ALEJANDRE
Affiliation:1. Ingeniería Molecular, Instituto Mexicano del Petroleo , Eje Central Lazaro Cárdenas 152, Colonia San Bartolo Atepehuacan, C.P. 07730, México DF;2. Ingeniería Molecular, Instituto Mexicano del Petroleo , Eje Central Lazaro Cárdenas 152, Colonia San Bartolo Atepehuacan, C.P. 07730, México DF;3. Departamento de Química , Universidad Autónoma Metropolitana-Iztapalapa , Av. San Rafael Atlixco 186, Colonia Vicentina, C.P. 09340, Del. Iztapalapa, Mexico DF
Abstract:Molecular dynamics simulations in the canonical ensemble have been performed to obtain the thermodynamic and transport properties of the Lennard-Jones fluid. The dispersion interactions were calculated using lattice sums. This method makes it possible to simulate the full potential avoiding the inclusion of the long range corrections (LRC) during or at the end of simulations. In the calculation of dynamic properties in bulk phases and thermodynamic quantities of inhomogeneous systems where the interface is physically present, in general the LRC cannot easily be included. By using the lattice sums method, the results are independent of the truncation of the potential. In the liquid-vapour interface simulations it is not necessary to make any pre-judgments about the form of the LRC formula to calculate coexisting properties such as the surface tension. The lattice sums method has been applied to evaluate how well the full interaction can be calculated in the liquid phase and in the liquid-vapour interface. In the liquid phase the pressure, configurational energy, diffusion coefficient and shear viscosity were obtained. The results of the thermodynamic properties are compared with those obtained using the spherically truncated and shifted (STS) potential with the LRC added at the end of simulations, and excellent agreement is found. The transport properties are calculated on different system sizes for a state near the triple point. The diffusion coefficient using the lattice sums method increases with the number of molecules, and the results are higher than those of the STS model truncated at 2.5σ (STS2.5). The shear viscosity does not show any system size dependence for systems with more than 256 molecules, and the lattice sums results are essentially the same as those for the STS2.5. In the liquid-vapour equilibria the coexisting densities and vapour pressures for the full potential agree well with those obtained using the Gibbs ensemble and the NPT + test particle methods. The surface tension using lattice sums and truncation of forces at 2.5σ agrees well with STS results using large system sizes and cutoff distances.
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