Anwei Qin

Excess volume of mixing and equation of state theories

Equation-of state theories of Flory and of Sanchez and Lacombe describe both enthalpy and volume of mixing of binary systems using single component properties and only one binary parameter X12. We have evaluated this parameter from literature enthalpy data for numerous mixtures of two aromatic hydrocarbons, of alkanes with aromatic compounds, and of alkanes with carbonyl compounds. We have used this X12 for calculation of excess volumes and compared the results with our previously measured experimental data. The agreement was fair for mixtures of two nonpolar components. Nevertheless, mixtures containing either cyclohexane or benzene displayed anomalies that could be traced to special packing of molecules in these compounds when pure. For mixtures of carbonyl compounds with alkanes, the theories predicted the qualitative trends correctly, but the quantitative agreement was rather poor. These results tend to support a model in which the enthalpy(cohesive energy) is inversely proportional to volume (as in the theories considered) only for dispersive interaction. When polar-polar interactions are involved, the dependence of excess volume on the excess enthalpy is much weaker.

THERMODYNAMICS OF LIQUID MIXTURES STUDIED BY LIGHT SCATTERING

Abstract The light scattering method for measuring interactions in binary mixtures has been applied to three groups of mixtures of carbonyl compounds with aromatic hydrocarbons; namely, alkyi acetate-benzene mixtures, alkyl acetate-toluene mixtures, and butanonearomatic hydrocarbon mixtures. The interaction coefficients are rather small and, within each group, they exhibit well defined trends. This behavior is explained as a result of a specific interaction between an electron accepting aromatic ring and an electron donating carbonyl.