Densities (rho) at various temperatures ranging from -10 up to +80 degrees C have been measured for N,N-dimethylformamide+2-methoxyethanol+1,2-dimethoxyethane ternary solvent system, employing 66 mixtures covering the whole miscibility field. Polynomial equations describing the dependence on temperature, rho=rho(t/degrees C), and molar composition, rho=rho(X(1),X(2)), have been checked. Furthermore, the excess molar volumes (V-E), derived from rho values, can provide useful suggestions about the formation of solvent-cosolvent complexes. Excess molar volumes have been interpreted on the basis of specific interactions between unlike molecules, taking into account geometric effects and steric hindrances. The V-E quantities have been isothermally fitted by an empirical relation of the type V-E=V-E(X(1),X(2),X(3)) formally derived from the well known Redlich-Kister equation. As a rule, for all the here tested relationships, the calculated values agree very well with the experimental ones, indicating that all the equations can be safely employed fdr predictive calculations in correspondence of the experimental data gaps.
Density and volumic properties of N,N-dimethylformamide +2-methoxyethanol+1,2-dimethoxyethane liquid ternary mixtures / F., Corradini; Marchetti, Andrea; M., Tagliazucchi; Tassi, Lorenzo. - In: BULLETIN OF THE CHEMICAL SOCIETY OF JAPAN. - ISSN 0009-2673. - ELETTRONICO. - 68:(1995), pp. 3373-3381.
Density and volumic properties of N,N-dimethylformamide +2-methoxyethanol+1,2-dimethoxyethane liquid ternary mixtures
MARCHETTI, Andrea;TASSI, Lorenzo
1995
Abstract
Densities (rho) at various temperatures ranging from -10 up to +80 degrees C have been measured for N,N-dimethylformamide+2-methoxyethanol+1,2-dimethoxyethane ternary solvent system, employing 66 mixtures covering the whole miscibility field. Polynomial equations describing the dependence on temperature, rho=rho(t/degrees C), and molar composition, rho=rho(X(1),X(2)), have been checked. Furthermore, the excess molar volumes (V-E), derived from rho values, can provide useful suggestions about the formation of solvent-cosolvent complexes. Excess molar volumes have been interpreted on the basis of specific interactions between unlike molecules, taking into account geometric effects and steric hindrances. The V-E quantities have been isothermally fitted by an empirical relation of the type V-E=V-E(X(1),X(2),X(3)) formally derived from the well known Redlich-Kister equation. As a rule, for all the here tested relationships, the calculated values agree very well with the experimental ones, indicating that all the equations can be safely employed fdr predictive calculations in correspondence of the experimental data gaps.Pubblicazioni consigliate
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