Related Experiment Video
Updated: Apr 21, 2026

High-pressure Sapphire Cell for Phase Equilibria Measurements of CO2/Organic/Water Systems
Published on: January 24, 2014
Universal thermodynamics at the liquid-vapor critical point
Isaac C Sanchez1, Kevin L Boening
1McKetta Chemical Engineering Department, University of Texas , Austin, Texas 78712, United States.
Abstract:
For 68 fluids that include hydrogen bonding and quantum fluids, the fugacity coefficient that defines the residual chemical potential adopts a near universal value of 2/3 at the critical point. More precisely, the reciprocal of the fugacity coefficient equals 1.52 ± 0.02 and includes fluids as diverse as helium (1.50), dodecafluoropentane (1.50), and water (1.53). For 65 classical fluids, a dimensionless thermal pressure coefficient and internal pressure attain critical values of 1.88 ± 0.11 and 1.61 ± 0.11, respectively. From equations of state, values of these new critical constants have been calculated and agree favorably with experimental values. Specifically, for the critical fugacity coefficient, the following results were obtained for its reciprocal: van der Waals (1.44), lattice gas (1.43), scaled particle theory (1.46), and the Redlich-Kwong eq (1.50). The semiempirical Redlich-Kwong equation is also the most accurate for the thermal pressure coefficient (1.86) and internal pressure (1.53). Physical interpretations of these results are discussed as well as their implications for other critical phenomena.
Related Concept Videos
pV-Diagrams
Thermodynamic Properties of Ideal Solutions
Vapor Pressure
Vapor Pressure of Fluid
When a liquid is placed in a closed container with a small air space, and the space is evacuated, vapor molecules will...
Distillation: Vapor–Liquid Equilibria
Two Components: Liquid–Liquid Systems

