Results 271 to 280 of about 225,293 (353)
Some of the next articles are maybe not open access.

Isobaric vapor-liquid equilibrium of a ternary system of ethyl acetate + propyl acetate + dimethyl sulfoxide and binary systems of ethyl acetate + dimethyl sulfoxide and propyl acetate + dimethyl sulfoxide at 101.3 kPa

Journal of Chemical Thermodynamics, 2019
Isobaric vapor-liquid equilibrium data were measured for three systems, namely, ethyl acetate + dimethyl sulfoxide, propyl acetate + dimethyl sulfoxide and ethyl acetate + propyl acetate + dimethyl sulfoxide at 101.3 kPa in this work.
Yinglong Wang   +6 more
semanticscholar   +1 more source

Vapor–liquid equilibrium of three binary systems for acetone, diethylamine and N-methyl pyrrolidone at atmospheric pressure

Journal of Molecular Liquids, 2019
The vapor liquid equilibrium data of diethylamine + acetone, acetone + N-methyl pyrrolidone and diethylamine + N-methyl pyrrolidone were measured at 101.3 kPa in this article. Van Ness and Herington test were used to check the experimental data.
Jingwei Yang   +5 more
semanticscholar   +1 more source

Vapor–liquid equilibrium for binary and ternary systems of tetrahydrofuran, ethyl acetate and N-methyl pyrrolidone at pressure 101.3 kPa

Journal of Molecular Liquids, 2018
Vapor−liquid equilibrium (VLE) data for the binary systems of tetrahydrofuran (THF) + ethyl acetate (EtOAc), THF + N-methyl pyrrolidone (NMP) and EtOAc + NMP, and the ternary systems of THF + EtOAc + NMP were measured at 101.3 kPa.
Jingwei Yang   +6 more
semanticscholar   +1 more source

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

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 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

Low Pressure Vapor-Liquid Equilibrium

1993
Separations using, Distillation, Extraction, Gas Absorption, etc., represent the main unit operations in the Chemical and Petroleum Industries, often reaching 50% of the total plant cost.
openaire   +1 more source

Home - About - Disclaimer - Privacy