Relating solute interactions to interfacial properties
Abstract
Liquid interfaces are both ubiquitous and also critically important for many commercial products, modern technologies, biological processes, and environmental phenomena. The properties of these interfaces can depend quite sensitively upon the composition of the bulk liquid phase. In this work, we develop a dilute solution theory (DST) for the influence of dilute cosolutes upon the interface between coexisting liquid and vapor phases. We employ a grand canonical perturbation theory to rigorously relate the interfacial free energy to the concentration of the liquid solution. We leverage a corresponding Gibbs ensemble to treat liquid-vapor coexistence and to eliminate the contribution of the bulk phases from this free energy. We express the coefficients of the resulting expansion in terms of microscopic partition functions. By treating solute-solute interactions to lowest order, we distinguish between the intrinsic and effective interfacial preferences of solutes. While the former reflects only solute-solvent interactions, the latter depends upon the solution composition and reflects the influence of solute-solute interactions. We assess this DST with molecular dynamics simulations of binary and ternary mixtures of Lennard-Jones spheres. These simulations demonstrate that DST accurately models the interfacial properties of these systems up to relatively high concentrations. Moreover, the simulations illustrate the impact of attractive solute-solute interactions in converting weak intrinsic surfactants into weak effective depletants.
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BibTeX
@misc{mandalaparthy2026relating,
title = {{Relating solute interactions to interfacial properties}},
author = {Varun Mandalaparthy and Benjamin M. Curlee and William G. Noid},
howpublished = {arXiv},
year = {2026},
month = sep,
doi = {10.48550/arxiv.2609.02762},
eprint = {2609.02762},
archivePrefix = {arXiv},
url = {https://arxiv.org/abs/2609.02762},
note = {CC BY 4.0},
}
RIS
TY - UNPB
TI - Relating solute interactions to interfacial properties
AU - Varun Mandalaparthy
AU - Benjamin M. Curlee
AU - William G. Noid
PY - 2026
DA - 2026/09/02
PB - arXiv
DO - 10.48550/arxiv.2609.02762
UR - https://arxiv.org/abs/2609.02762
AB - Liquid interfaces are both ubiquitous and also critically important for many commercial products, modern technologies, biological processes, and environmental phenomena. The properties of these interfaces can depend quite sensitively upon the composition of the bulk liquid phase. In this work, we develop a dilute solution theory (DST) for the influence of dilute cosolutes upon the interface between coexisting liquid and vapor phases. We employ a grand canonical perturbation theory to rigorously relate the interfacial free energy to the concentration of the liquid solution. We leverage a corresponding Gibbs ensemble to treat liquid-vapor coexistence and to eliminate the contribution of the bulk phases from this free energy. We express the coefficients of the resulting expansion in terms of microscopic partition functions. By treating solute-solute interactions to lowest order, we distinguish between the intrinsic and effective interfacial preferences of solutes. While the former reflects only solute-solvent interactions, the latter depends upon the solution composition and reflects the influence of solute-solute interactions. We assess this DST with molecular dynamics simulations of binary and ternary mixtures of Lennard-Jones spheres. These simulations demonstrate that DST accurately models the interfacial properties of these systems up to relatively high concentrations. Moreover, the simulations illustrate the impact of attractive solute-solute interactions in converting weak intrinsic surfactants into weak effective depletants.
ER -