Phase-field models for particle-stabilized emulsions

Particle-stabilized emulsions are a cornerstone of soft matter science due to their broad applications and fundamental relevance. Computer simulations provide key insights into the formation and behavior of these emulsions; yet, current methods are limited by the spatiotemporal scales accessible for study. The principal issue is that particles are resolved individually. In this work, an alternative strategy is introduced based on phase-field theory, for which we establish the framework. By evolving continuous fields, large-scale dynamics can be simulated in a computationally efficient manner. Our approach is then applied to model the complex formation of a bicontinuous interfacially jammed emulsion gel (bijel) via solvent-transfer-induced phase separation (STrIPS). By resolving the coupled dynamics of liquid phase separation and nanoparticle adsorption, the model allows for the characterization of the influence of nanoparticles on the morphology. Higher concentrations of nanoparticles are found to reduce the average domain size of STrIPS bijels, in line with previous experimental evidence. The presented phase-field model thus represents a promising approach for the morphological investigation of complex particle-stabilized emulsions.

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Publication Details

Journal
The Journal of Chemical Physics
Published
2026-03-23
DOI
https://doi.org/10.1063/5.0329556
Primary Topic
Block Copolymer Self-Assembly
Type
article
Field-Weighted Citation Impact
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article

Phase-field models for particle-stabilized emulsions

Joost de Graaf, Jesse M. Steenhoff, Martin F. Haase, Elisabeth C. Eij
The Journal of Chemical Physics
Block Copolymer Self-Assembly
article

Phase-field models for particle-stabilized emulsions

Joost de Graaf, Jesse M. Steenhoff, Martin F. Haase, Elisabeth C. Eij
article en

Abstract

Particle-stabilized emulsions are a cornerstone of soft matter science due to their broad applications and fundamental relevance. Computer simulations provide key insights into the formation and behavior of these emulsions; yet, current methods are limited by the spatiotemporal scales accessible for study. The principal issue is that particles are resolved individually. In this work, an alternative strategy is introduced based on phase-field theory, for which we establish the framework. By evolving continuous fields, large-scale dynamics can be simulated in a computationally efficient manner. Our approach is then applied to model the complex formation of a bicontinuous interfacially jammed emulsion gel (bijel) via solvent-transfer-induced phase separation (STrIPS). By resolving the coupled dynamics of liquid phase separation and nanoparticle adsorption, the model allows for the characterization of the influence of nanoparticles on the morphology. Higher concentrations of nanoparticles are found to reduce the average domain size of STrIPS bijels, in line with previous experimental evidence. The presented phase-field model thus represents a promising approach for the morphological investigation of complex particle-stabilized emulsions.

The Journal of Chemical PhysicsVol. 164(12)
University of Applied Sciences Utrecht (NL), Utrecht University (NL), Instituto de Física Teórica (ES)
Openalex Percentile: Top 13%
Block Copolymer Self-Assembly
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