Vapor pressures and vapor liquid equilibria in the systems: (1) acetone – chloroform, (2) acetone – carbon tetrachloride, (3) benzene – carbon tetrachloride

1970 ◽  
Vol 48 (20) ◽  
pp. 3173-3184 ◽  
Author(s):  
A. N. Campbell ◽  
G. M. Musbally

The saturation vapor pressures of ten mixtures of the binary systems (1) acetone – chloroform, (2) acetone – carbon tetrachloride, and (3) benzene – carbon tetrachloride have been determined, from 100 to 230° for system 1 and from 100° up to the highest temperature at which liquid and vapor coexist for systems 2 and 3. The system acetone – chloroform could not be studied at higher temperatures because of decomposition.The gas–liquid critical temperatures of the three binary systems have been determined by the disappearance of meniscus method. The orthobaric compositions of the vapour–liquid equilibria of the binary systems have been measured from 100 to 180° for system 1 and from 100° to the critical region for systems 2 and 3, using a glass bomb enclosed in a steel bomb.From the vapour–liquid composition curves and the vapor pressure curves at constant temperatures (100, 150, 160, 170, and 180°), the existence of an azeotrope in the system acetone–chloroform at these temperatures, and having a composition of 36.2 mole% acetone at 100°, was confirmed. The composition of the azeotrope shifts towards lower acetone content as the temperature is raised. Azeotropes were not found in the systems acetone – carbon tetrachloride and benzene – carbon tetrachloride, over the ranges of temperature and pressure of this research.The data of the binary systems were treated thermodynamically to yield the liquid phase activity coefficients and, as suggested by Chueh and Prausnitz, the Redlick–Kwong equation was used in a modified form to obtain the fugacity coefficients of components in the vapor phase. Several liquid phase parameters, such as the binary interaction constant, Henry's constant, and dilation constant have been calculated, using the van Laar equation as modified by Chueh and Prausnitz.

1970 ◽  
Vol 48 (2) ◽  
pp. 277-285 ◽  
Author(s):  
A. N. Campbell ◽  
R. M. Chatterjee

The saturation pressures and vapor–liquid compositions of 7 mixtures of the system acetone–benzene have been determined from a temperature of 100 °C and a pressure of about 2 atm up to the highest temperatures and pressures at which liquid and vapor coexist. The critical temperatures were determined by the disappearance-of-meniscus method.The P–T–X relations at the liquid–vapor phase boundaries, as obtained by the determination of the bubble-point pressure vs. temperature curves of a series of mixtures of known composition, do not indicate the existence of an azeotrope in the range of temperature and pressure of this research. The binary data have been treated thermodynamically to yield the liquid-phase activity coefficients. The partial molal volumes in the liquid mixture required for the Poynting correction (effect of pressure on liquid phase properties) for liquid-phase activity coefficients have also been obtained. The fugacity coefficient of a component in the vapor mixture has been obtained by a modified Redlich–Kwong equation, as suggested by Chueh and Prausnitz. Following their modification of the van Laar equation, several binary liquid phase parameters, such as the binary interaction constant, Henry's constant and dilation constant, as required for the solution model for excess Gibbs energy, have been calculated.


2021 ◽  
Author(s):  
Simon Stephan ◽  
Hans Hasse

Properties of vapor-liquid equilibria and planar interfaces of binary Lennard-Jones truncated and shifted mixtures were investigated with molecular dynamics simulations, density gradient theory, and conformal solution theory at constant liquid phase composition and temperature. The results elucidate the influence of the liquid phase interactions on the interfacial properties (surface tension, surface excess, interfacial thickness, and enrichment). The studied mixtures differ in the ratios of the dispersion energies of the two components ɛ2/ɛ1 and the binary interaction parameter ξ. By varying ξ and ɛ2/ɛ1, a variety of types of phase behavior is covered by this paper. The dependence of the interfacial properties on the variables ξ and ɛ2/ɛ1 reveals regularities that can be explained by conformal solution theory of the liquid phase. It is thereby shown that the interfacial properties of the mixtures are dominated by the mean liquid phase interactions whereas the vapor phase has only a minor influence.


Fluids ◽  
2021 ◽  
Vol 6 (10) ◽  
pp. 354
Author(s):  
Otto G. Piringer

In this manuscript, a function is derived that allows the interactions between the atoms/molecules in nanoparticles, nanodrops, and macroscopic liquid phases to be modeled. One goal of molecular theories is the development of expressions to predict specific physical properties of liquids for which no experimental data are available. A big limitation of reliable applications of known expressions is that they are based on the interactions between pairs of molecules. There is no reason to suppose that the energy of interaction of three or more molecules is the sum of the pairwise interaction energies alone. Here, an interaction function with the limit value w = e2π/e is presented, which allows for the derivation of the atomic mass unit and acts as a bridge between properties of elementary particles and emergent properties of macroscopic systems. The following properties of liquids are presented using the introduced interaction function: melting temperatures of n-alkanes, nanocrystals of polyethylene, melting temperatures of metal nanoparticles, solid–liquid phase transition temperatures for water in nanopores, critical temperatures and critical pressures of n-alkanes, vapor pressures in liquids and liquid droplets, self-diffusion coefficients of compounds in liquids, binary liquid diffusion coefficients, diffusion coefficients in liquids at infinite dilution, diffusion in polymers, and viscosities in liquids.


Molecules ◽  
2021 ◽  
Vol 26 (2) ◽  
pp. 460
Author(s):  
Ratna Surya Alwi ◽  
Chandrasekhar Garlapati ◽  
Kazuhiro Tamura

Solubility of several anthraquinone derivatives in supercritical carbon dioxide was readily available in the literature, but correcting ability of the existing models was poor. Therefore, in this work, two new models have been developed for better correlation based on solid–liquid phase equilibria. The new model has five adjustable parameters correlating the solubility isotherms as a function of temperature. The accuracy of the proposed models was evaluated by correlating 25 binary systems. The proposed models observed provide the best overall correlations. The overall deviation between the experimental and the correlated results was less than 11.46% in averaged absolute relative deviation (AARD). Moreover, exiting solubility models were also evaluated for all the compounds for the comparison purpose.


Sign in / Sign up

Export Citation Format

Share Document