Theory of nonionic hydrophobic solutes in mixture solvent: Solvent-mediated interaction and solute-induced phase separation
Ryuichi Okamoto, Akira Onuki

TL;DR
This paper develops a theoretical framework for understanding how nonionic hydrophobic solutes interact within a mixture solvent, revealing how solute density couples with solvent composition and induces phase separation.
Contribution
It introduces a comprehensive theory linking solvation properties, thermodynamic coupling, and phase behavior of nonionic solutes in mixed solvents, including phase transition predictions.
Findings
Large solute-solute attraction due to solvent fluctuations.
Derived solute spinodal density for instability.
Predicted phase diagrams for 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,…
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