Related Experiment Video
Updated: Nov 27, 2025

High-pressure Sapphire Cell for Phase Equilibria Measurements of CO2/Organic/Water Systems
Published on: January 24, 2014
Vapor-liquid equilibria and cohesive r-4 interactions
1Centre for Computational Innovations, Swinburne University of Technology, P.O. Box 218, Hawthorn, Victoria 3122, Australia.
Abstract:
The role of cohesive r-4 interactions on the existence of a vapor phase and the formation of vapor-liquid equilibria is investigated by performing molecular simulations for the n-4 potential. The cohesive r-4 interactions delay the emergence of a vapor phase until very high temperatures. The critical temperature is up to 5 times higher than normal fluids, as represented by the Lennard-Jones potential. The greatest overall influence on vapor-liquid equilibria is observed for the 5-4 potential, which is the lowest repulsive limit of the potential. Increasing n initially mitigates the influence of r-4 interactions, but the moderating influence declines for n > 12. A relationship is reported between the critical temperature and the Boyle temperature, which allows the critical temperature to be determined for a given n value. The n-4 potential could provide valuable insight into the behavior of non-conventional materials with both very low vapor pressures at elevated temperatures and highly dipolar interactions.
Related Concept Videos
Vapor Pressure
Vapor Pressure Lowering
Clausius-Clapeyron Equation
Phase Transitions: Vaporization and Condensation
Ideal Solutions
Van der Waals Equation
First, the attractive forces between molecules, which are stronger at higher densities and reduce the pressure, are considered by adding to the pressure a term equal to the square of the molar density multiplied by a positive coefficient a. Second, the volume...

