English

Theory of nonionic hydrophobic solutes in mixture solvent: Solvent-mediated interaction and solute-induced phase separation

Soft Condensed Matter 2018-08-01 v1

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 viv_i, the Kirkwood-Buff integrals, the second osmotic virial coefficient, and the Gibbs transfer free energy. We examine how the solute density n3n_3 is coupled to the solvent densities n1n_1 and n2n_2 in thermodynamics. In the limit of small compressibility, we show that the space-filling condition ivini=1\sum_i v_i n_i=1 nearly holds for inhomogeneous densities nin_i, where the concentration fluctuations of the solvent can give rise to a large solute-solute attractive interaction. We also derive a solute spinodal density n3spin_3^{\rm spi} 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