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Research PaperResearchia:202601.29224[Chemical Physics > Chemistry]

The roles of bulk and surface thermodynamics in the selective adsorption of a confined azeotropic mixture

Katie L. Y. Zhou

Abstract

Fluid mixtures that exhibit an azeotrope cannot be purified by simple bulk distillation. Consequently, there is strong motivation to understand the behavior of azeotropic mixtures under confinement. We address this problem using a machine-learning-enhanced classical density functional theory applied to a binary Lennard-Jones mixture that exhibits azeotropic phase behavior. As proof-of-principle of a "train once, learn many" strategy, our approach combines a neural functional trained on a single-component repulsive reference system with a mean-field treatment of attractive interactions, derived within the framework of hyperdensity functional theory (hyper-DFT). The theory faithfully describes capillary condensation and results from grand canonical Monte Carlo simulations. Moreover, by taking advantage of a known accurate equation of state, the theory we present well-describes bulk thermodynamics by construction. Exploiting the computational efficiency of hyper-DFT, we systematically evaluate adsorption selectivity across a wide range of compositions, pressures, temperatures, and wall-fluid affinities. In cases where the wall-fluid interaction is the same for both species, we find that the pore becomes completely unselective at the bulk azeotropic composition. Strikingly, this unselective point persists far from liquid-vapor coexistence, including in the supercritical regime. Analysis of the bulk equation of state across a wide range of thermodynamic state points shows that the azeotropic composition coincides with equal partial molar volumes and an extremum in the isothermal compressibility. A complementary thermodynamic analysis demonstrates that unselective adsorption corresponds to an aneotrope (a point of zero relative adsorption) and an extremum in the interfacial free energy. We also find that the two interfaces of the slit pore behave independently down to remarkably small slits.


Source: arXiv:2601.21591v1 - http://arxiv.org/abs/2601.21591v1 PDF: https://arxiv.org/pdf/2601.21591v1 Original Link: http://arxiv.org/abs/2601.21591v1

Submission:1/29/2026
Comments:0 comments
Subjects:Chemistry; Chemical Physics
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arXiv: This paper is hosted on arXiv, an open-access repository
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