Heats of dilution of ternary aqueous solutions containing alkan-1-ols and alkane-1,2-diols or alkane-alpha,omega -diols have been determined at 298.15 K by flow microcalorimetry. The pairwise interaction coefficients of the virial expansion of the excess enthalpies were evaluated and compared to those formerly obtained for binary aqueous solutions of alkan-m-ols or alkane-m,n-diols. The results were interpreted using the "preferential configuration" model, namely in terms of preferential interactions between hydrophilic domains and of repulsive interactions between hydrophobic and hydrophilic domains. Hydroxyl groups present a different efficiency in promoting hydrophobic interactions in dependence of their number and position in the interacting molecules. (C) 2000 Elsevier Science B.V. All rights reserved.
Efficiency of hydroxyl groups in promoting hydrophobic interactions. A calorimetric study of ternary aqueous solutions of alkan-1-ols and alkane-m,n-diols / Castronuovo, Giuseppina; V., Elia; S., Perez Casas; F., Velleca. - In: JOURNAL OF MOLECULAR LIQUIDS. - ISSN 0167-7322. - STAMPA. - 88:(2000), pp. 163-173. [10.1016/S0167-7322(00)00151-3]
Efficiency of hydroxyl groups in promoting hydrophobic interactions. A calorimetric study of ternary aqueous solutions of alkan-1-ols and alkane-m,n-diols.
CASTRONUOVO, GIUSEPPINA;
2000
Abstract
Heats of dilution of ternary aqueous solutions containing alkan-1-ols and alkane-1,2-diols or alkane-alpha,omega -diols have been determined at 298.15 K by flow microcalorimetry. The pairwise interaction coefficients of the virial expansion of the excess enthalpies were evaluated and compared to those formerly obtained for binary aqueous solutions of alkan-m-ols or alkane-m,n-diols. The results were interpreted using the "preferential configuration" model, namely in terms of preferential interactions between hydrophilic domains and of repulsive interactions between hydrophobic and hydrophilic domains. Hydroxyl groups present a different efficiency in promoting hydrophobic interactions in dependence of their number and position in the interacting molecules. (C) 2000 Elsevier Science B.V. All rights reserved.I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.