Modified PT-LJ-SAFT Density Functional Theory: I. Prediction of surface properties and phase equilibria of non-associating fluids

Abstract

Listen

Translate article

A new modified version of a Perturbation Density Functional Theory (PT-DFT) based on the Statistical Association Fluid Theory (SAFT) with a Lennard–Jones interaction potential is proposed to model the vapor–liquid phase equilibrium and to predict the interfacial behavior of non-associating hydrocarbon fluids. In the interaction model for the Helmholtz free energy functional the molecules are separated into m spherical segments interacting via a Lennard–Jones potential. The segments form chains of tangent spheres. In the perturbation approximation to Density Functional Theory the interaction potential is split according to WCA and the attractive term to the free energy functional consists of a suitable modification of the perturbation expression. This modification to PT-DFT yields surface tensions for the Lennard–Jones sphere fluid ( m = 1.0) which are in perfect agreement with simulation data. The new PT-DFT model combines the high flexibility of the SAFT free energy functional with a modified density functional approach that enables to perform accurate calculations of interfacial properties. To take into account the contributions to surface tension resulting from mesoscale thermal fluctuations a semiempirical model is proposed that allows to correct the microscopic intrinsic surface tension. The model is used to describe the phase equilibrium of lower alkanes and aromatics. The results demonstrate the capability to fit vapor–liquid equilibrium data and to predict very accurately the surface properties of these fluids within the uncertainties of the experimental data.