Journal of Chemical Engineering of Japan, Vol.31, No.4, 518-526, 1998
An improved model of second virial coefficients for polar fluids and fluid mixtures
A corresponding-states model was developed empirically for calculating the second virial coefficients of polar fluids and fluid mixtures. In this model, a "nonpolar" and a "polar" acentric factors characterize size/shape and polarity/association effects, respectively. The new model contains a polarity or an association parameter (alpha(P) or alpha(HB)), which can be estimated from fluid's reduced dipole moment through a specific generalized correlation. The temperature function of association contribution was found to depend on fluid's reduced dipole moment. This generalized model predicts well the second virial coefficients for a diversity of polar fluids and strongly hydrogen-bonded substances. The new model with a set of recommended k(ij)'s can reasonably estimate the second virial cross-coefficients.
Keywords:CORRESPONDING-STATES METHOD;EXCESS MOLAR ENTHALPIES;THERMODYNAMIC PROPERTIES;BINARY-MIXTURES;VAPOR-PRESSURES;WATER;GASES;COMPONENTS;EQUATION;METHANE