Abstract
ABSTRACTThe solution behavior of solvophobic polymers is crucial to the development of polymer coatings and polymeric drug delivery vehicles. In this article, the role of dipolar interactions is investigated in the solvophobic coalescence of polystyrene in binary correlated polar solvent mixtures. A simple model for coalescence thermodynamics is derived from correlations between thermally rotating dipole moments in the solvent. The stabilizing correlations lost to the solvent due to a solute's presence give rise to a driving force for the coalescence of solutes. This stabilization is offset by the entropy of mixing that favors the dispersion of solutes. Predictions are compared to the measured point of coalescence of polystyrene in acetone when different alcohols are titrated. The model is shown to capture this point of coalescence and conformation for a variety of systems. Our results suggest the significant property determining the solubility of nonpolar polymers in a polar liquid is a free energy resulting from attractive dispersion interactions between thermally rotating solvent dipole moments. © 2016 Wiley Periodicals, Inc. J. Polym. Sci., Part B: Polym. Phys. 2016, 54, 948–955
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