Thermodynamic stability of droplets, bubbles and thick films in open and closed pores
Magnus Aa. Gjennestad, {\O}ivind Wilhelmsen

TL;DR
This study investigates the thermodynamic stability of droplets, bubbles, and films of water in pores, revealing how pore size, shape, and boundary conditions influence stability and metastability through a combined capillary and equation of state approach.
Contribution
It introduces a new methodology for analyzing film stability and provides comprehensive phase diagrams for heterogeneous structures in different pore conditions.
Findings
Large pores' stability governed by mechanical stability.
Films in closed pores are often metastable.
Open pores favor homogeneous or droplet/bubble phases.
Abstract
A fluid in a pore can form diverse heterogeneous structures. We combine a capillary description with the cubic-plus-association equation of state to study the thermodynamic stability of droplets, bubbles and films of water at 358 K in a cylindrically symmetric pore. The equilibrium structure depends strongly on the size of the pore and whether the pore is closed or connected to a particle reservoir. A new methodology is presented to analyze the thermodynamic stability of films, where the integral that describes the total energy of the system is approximated by a quadrature rule. We show that, for large pores, the thermodynamic stability limit of adsorbed droplets and bubbles in both open and closed pores is governed by their mechanical stability, which is closely linked to the pore shape. This is also the case for a film in a closed pore. In open pores, the film is chemically unstable…
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