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Isobaric vapor–liquid and vapor–liquid–liquid equilibrium data for the system water+ethanol+cyclohexane [PDF]

open access: yesFluid Phase Equilibria, 2005
Isobaric vapor–liquid (VLE) and vapor–liquid–liquid equilibria (VLLE) were measured for the ternary system water + ethanol + cyclohexane at 101.3 kPa. The experimental determination was carried out in a dynamic equilibrium still with circulation of both
Alicia Font, V Gomis
exaly   +2 more sources

Isothermal (liquid + liquid) equilibrium data at T= 313.15 K and isobaric (vapor + liquid + liquid) equilibrium data at 101.3 kPa for the ternary system (water + 1-butanol + p-xylene)

open access: yesJournal of Chemical Thermodynamics, 2014
The (vapor + liquid), (liquid + liquid) and (vapor + liquid + liquid) equilibria of the ternary system (water + 1-butanol + p-xylene) have been determined.
Vicente Gomis Yagües   +2 more
exaly   +2 more sources
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Molecular Simulations of Vapor–Liquid Equilibrium of Isocyanates

The Journal of Physical Chemistry B, 2021
The wide range of applications of the isocyanates across multiple industries sparks the interest in the study of their phase behavior. A molecular simulation is a powerful tool that can go beyond experimental investigations relying on a molecular structure of a chemical.
Alina Emelianova, Gennady Y. Gor
openaire   +2 more sources

Vapor−Liquid Equilibrium in Electric Field Gradients

The Journal of Physical Chemistry B, 2010
We investigate the vapor-liquid coexistence of polar and nonpolar fluids in the presence of a nonuniform electric field. We find that a large enough electric field can nucleate a gas bubble from the liquid phase or a liquid droplet from the vapor phase. The surface tension of the vapor-liquid interface is determined within squared-gradient theory. When
Sela Samin, Yoav Tsori
openaire   +2 more sources

Vapor–Liquid Equilibrium

2010
Every time a fluid is confined at a nanometer scale, the predominance of the fluid–substrate interactions strongly distorts its intrinsic properties. For instance, it is observed that the amount of fluid adsorbed in a nanoporous substrate is not a single-valued function of the chemical potential and may present a hysteresis.
openaire   +1 more source

Vapor-liquid equilibrium in capillary distillation

Desalination, 1991
Abstract With the advent of capillary distillation (12, 28, 29 30, 31,32) vapor-liquid equilibrium data of solutions in small capillaries have become important. These data for various alcohol-water mixtures have been obtained and published recently (13). Although the experimental method used is simple, it is very time-consuming.
G.C. Yeh   +5 more
openaire   +1 more source

Vapor-liquid equilibrium of methyl chloride

AIP Conference Proceedings, 1995
An intermolecular site‐site (CH3 and Cl) potential has been used with the Gibbs ensemble Monte Carlo method to calculate the vapor‐liquid equilibrium coexistence and critical properties of methyl chloride. The calculations have been carried out in the triple point (175 K)‐critical point (417 K) range.
F. F. Martins Freitas   +1 more
openaire   +1 more source

Group contributions in vapor‐liquid equilibrium

The Canadian Journal of Chemical Engineering, 1969
AbstractAn empirical method has been developed for the prediction of vapor‐liquid equilibrium data, both composition and temperature, for a series of binaries of chain hydrocarbons with carbon tetrachloride. The maximum and absolute average deviations in vapor composition are 0.035 and 0.006 mole fraction, respectively, and in temperature are 1.5 and 0.
Alan J. Rodger   +2 more
openaire   +1 more source

Vapor-Liquid Equilibrium

Industrial & Engineering Chemistry, 1954
Ju Chin Chu   +3 more
openaire   +1 more source

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