APPLICATION OF QUASI-LATTICE THEORY TO ALCOHOL – CARBON TETRACHLORIDE SYSTEMS

1963 ◽  
Vol 41 (2) ◽  
pp. 278-286 ◽  
Author(s):  
B. Dacre ◽  
G. C. Benson
Keyword(s):  
Carbon Tetrachloride ◽  
Thermodynamic Functions ◽  
Lattice Theory ◽  
Experimental Results ◽  
Heats Of Mixing ◽  
Excess Thermodynamic Functions

Values of heats of mixing are reported for methanol, n-butanol, and n-octanol with carbon tetrachloride at 25 °C. The experimental results are combined with data from other sources and an analysis of the excess thermodynamic functions for carbon tetrachloride solutions of methanol, ethanol, n-propanol, n-butanol, and n-octanol in terms of Barker's theory of solutions is described. The behavior of these systems can be reproduced fairly well by the Barker model.

The statistical thermodynamics of solutions of non-spherical molecules. I. The thermodynamic functions

1955 ◽  
Vol 229 (1177) ◽  
pp. 271-280 ◽  
Keyword(s):  
Carbon Tetrachloride ◽  
Equation Of State ◽  
Thermodynamic Functions ◽  
Statistical Thermodynamics ◽  
Intermolecular Forces ◽  
Pure Component ◽  
Experimental Results ◽  
Thermodynamics Of Solutions ◽  
Theory And Experiment

The perturbation treatment of the orientational forces between non-spherical molecules proposed by Cook & Rowlinson (1953) is extended to mixtures by using the theory of solutions put forward by Longuet-Higgins (1951). The thermodynamic functions and the equation of state of such mixtures are expressed in terms of the intermolecular forces and the properties of one pure component. Expressions are derived for the excess (or non-ideal) thermodynamic functions which are compared with the experimental results on the four solutions, benzene+ cyclohexane , benzene+carbon tetrachloride, benzene + ethylene dychloride, and cyclohexane + carbon tetrachloride. The agreement between theory and experiment is improved by taking account of the orientational forces.

Réactions dans le sulfolane. III. Etude des interactions eau–sulfolane

1968 ◽  
Vol 46 (20) ◽  
pp. 3215-3219 ◽  
Author(s):  
R. L. Benoit ◽  
G. Choux
Keyword(s):  
Water Activity ◽  
Thermodynamic Functions ◽  
Proton Acceptor ◽  
Acidity Function ◽  
Vapor Pressures ◽  
Heat Of Solution ◽  
Sulfone Group ◽  
Heats Of Mixing ◽  
Excess Thermodynamic Functions ◽  
System Water

Heats of mixing at 30 °C and vapor pressures at 30, 40, and 50 °C have been measured for the system water–sulfolane. The excess thermodynamic functions ΔGE, ΔHM, and ΔSE have been calculated. The value of the heat of solution [Formula: see text] indicates that the sulfone group is a weak proton acceptor. The effects of water activity on the H− acidity function values in hydroxide media have been compared for the systems water–sulfolane and water–dimethylsulfoxide.

Excess thermodynamic functions of cyclopentane-carbon tetrachloride mixtures

1969 ◽  
Vol 73 (7) ◽  
pp. 2356-2360 ◽  
Author(s):  
T. Boublik ◽  
V. T. Lam ◽  
S. Murakami ◽  
George C. Benson
Keyword(s):  
Carbon Tetrachloride ◽  
Thermodynamic Functions ◽  
Excess Thermodynamic Functions

Heats of mixing of binary mixtures of pyridine base with n-alkane

1988 ◽  
Vol 66 (7) ◽  
pp. 1625-1627 ◽  
Author(s):  
Teresa Kasprzycka-Guttman ◽  
Juan H. Vera
Keyword(s):  
Experimental Data ◽  
Binary Mixtures ◽  
Experimental Results ◽  
Pyridine Base ◽  
Heats Of Mixing

Heats of mixing of 2,4-lutidine and 2,4,6-collidine with n-alkanes were measured at 293.15 K using an isothermal dilution calorimeter. Experimental results were fitted with a Redlich–Kister polynomial. Experimental data and coefficients for the Redlich–Kister polynomials are reported.

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