Abstract
The present study reports result from research into vapor–liquid–liquid phase equilibrium for n-octane highly diluted in water and water highly diluted in n-octane blends, using a dynamic method implemented in a constant volume CREC-VL-Cell. In the CREC-VL-Cell, a very high level of mixing is achieved, allowing for dispersions to be formed in the liquid phase and good mixing in the gas phase. This VL-Cell and its auxiliary equipment provide an increasing temperature ramp in the 30–110 °C range. It is found that the CREC-VL-Cell is of special value, for studying immiscible or partially miscible blends, such as is the case of n-octane in water. With the data obtained, which includes vapor pressures and temperatures, data analyses involving mass and molar balances, allow establishing overall liquid and vapor molar fractions. The recorded vapor pressures together with the calculated liquid and vapor molar fractions offer valuable data for VL thermodynamic model discrimination. For instance, it can be shown that vapor pressures, vapor and liquid molar fractions, as calculated with the Aspen-Hysys Peng Robinson Equation of State (Hysys-Aspen PR-EoS) provide only a first approximation of the experimental data, with significant discrepancies in the prediction of an n-octane disengagement temperatures. Thus, the determination of combined measured vapor pressures and calculated overall liquid molar fractions in the CREC-VL-Cell, offers a valuable and accurate procedure for thermodynamic model validation and discrimination.
Thermodynamic Model of Liquid−Liquid Phase Equilibrium in Solutions of Alkanethiol-Coated Nanoparticles
