Theory of nonionic hydrophobic solutes in mixture solvent: Solvent-mediated interaction and solute-induced phase separation
Abstract
We present a theory of nonionic solutes in a mixture solvent composed of water-like and alcohol-like species. First, we show relationship among the solvation chemical potential, the partial volumes , the Kirkwood-Buff integrals, the second osmotic virial coefficient, and the Gibbs transfer free energy. We examine how the solute density is coupled to the solvent densities and in thermodynamics. In the limit of small compressibility, we show that the space-filling condition nearly holds for inhomogeneous densities , where the concentration fluctuations of the solvent can give rise to a large solute-solute attractive interaction. We also derive a solute spinodal density for solute-induced instability. Next, we examine gas-liquid and liquid-liquid phase transitions induced by a small amount of a solute using the Mansoori, Carnahan, Starling, and Leland model for hard-sphere mixtures { J. Chem. Phys.} {\bf 54}, 1523 (1971). Here, we assume that the solvent is close to its gas-liquid coexistence and the solute interacts repulsively with the water-like species but attractively with the alcohol-like one. We calculate the binodal and spinodal curves in the phase diagrams and examine nucleation for these two phase transitions.
Keywords
Cite
@article{arxiv.1806.05755,
title = {Theory of nonionic hydrophobic solutes in mixture solvent: Solvent-mediated interaction and solute-induced phase separation},
author = {Ryuichi Okamoto and Akira Onuki},
journal= {arXiv preprint arXiv:1806.05755},
year = {2018}
}
Comments
19 pages, 14 figures, accepted for publication in J. Chem. Phys