The molar surface Gibbs energy and its application to the binary mixtures of N-butylpyridinium dicyanamide [C4py][DCA] with alcohols

The density and surface tension for the binary mixtures of ionic liquid (IL) [C4py][DCA] with ethanol, 1-propanol and 2-propanol were measured across the entire range of mole fraction (x1 = 0.0000-1.0000) at T = (288.15-318.15) K. The average molar volume and the thermal expansion coefficient of the binary mixtures were calculated from the experimental density. The excess molar volumes, VE, of the binary mixtures were also calculated and well fitted by Redlich−Kister equation. The obtained VE are negative values over the whole composition range. The values of VE are related to the alcohol chain length and temperature. In order to predict the surface tension of the mixtures, the new function - the molar surface Gibbs energy of mixtures was obtained from Li's model improved by us in this work. So, the molar surface Gibbs energy, gs, and its excess function, gsE, of mixtures for [C4py][DCA] with ethanol, 1-propanol and 2-propanol were calculated. The excess molar surface Gibbs energy, gsE, was well fitted by Redlich−Kister equation. In terms of the Redlich−Kister's parameters, a new method for predicting the surface tension, γ, of the mixtures is proposed and the predicted values, γ (pre.), are in good agreement with the corresponding experimental ones, γ(exp.). On a basis of molar surface Gibbs energy of mixtures, a new EÓ§tvÓ§s equation was obtained and applied to binary mixtures of [C4py][DCA] with alcohols. The absolute value of the slope of the new Eötvös equation is the mole surface entropy, s, and the intercept is the molar surface enthalpy, h, which is temperature-independent.