Hydrodynamic simulation of viscoelastic phase separation via coupled Model–H and Oldroyd–B equations

Viscoelastic phase separation governs the nonequilibrium demixing dynamics of soft-matter systems. Here, we introduce an efficient continuum framework that couples the Cahn-Hilliard phase-field model with the Oldroyd-B constitutive equation. By treating the mixture as a single incompressible fluid, our model captures macromolecular deformation through a continuous conformation tensor and reveals distinct kinetic pathways across different thermodynamic regimes. In the spinodal regime, the minority polymer-rich phase undergoes morphological inversion into a persistent interconnected network, sustained by intense velocity gradients that stretch polymer chains and generate elastic stresses that suppress coarsening. In the nucleated-droplet regime, the model reveals strain-induced coarsening acceleration, in which highly elongated domains enhance the initial coalescence rate before elastic arrest sets in as the relaxation time increases. Tuning the rheological parameters recovers the classical Newtonian regime, demonstrating that this framework provides a simple, efficient, and robust platform for modeling phase separation in complex fluids.

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Publication Details

Journal
The Journal of Chemical Physics
Published
2026-09-01
DOI
https://doi.org/10.1063/5.0346272
Primary Topic
Block Copolymer Self-Assembly
Type
article
Field-Weighted Citation Impact
0.00

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article

Hydrodynamic simulation of viscoelastic phase separation via coupled Model–H and Oldroyd–B equations

Dixi Yang, Jiaxing Yuan
The Journal of Chemical Physics
Block Copolymer Self-Assembly
article

Hydrodynamic simulation of viscoelastic phase separation via coupled Model–H and Oldroyd–B equations

Dixi Yang, Jiaxing Yuan
article en

Abstract

Viscoelastic phase separation governs the nonequilibrium demixing dynamics of soft-matter systems. Here, we introduce an efficient continuum framework that couples the Cahn-Hilliard phase-field model with the Oldroyd-B constitutive equation. By treating the mixture as a single incompressible fluid, our model captures macromolecular deformation through a continuous conformation tensor and reveals distinct kinetic pathways across different thermodynamic regimes. In the spinodal regime, the minority polymer-rich phase undergoes morphological inversion into a persistent interconnected network, sustained by intense velocity gradients that stretch polymer chains and generate elastic stresses that suppress coarsening. In the nucleated-droplet regime, the model reveals strain-induced coarsening acceleration, in which highly elongated domains enhance the initial coalescence rate before elastic arrest sets in as the relaxation time increases. Tuning the rheological parameters recovers the classical Newtonian regime, demonstrating that this framework provides a simple, efficient, and robust platform for modeling phase separation in complex fluids.

The Journal of Chemical PhysicsVol. 165(9)
Guangzhou University (CN), Guangzhou Institute of Advanced Technology (CN), University of Hong Kong (HK)
National Natural Science Foundation of China, Guangdong Provincial Pearl River Talents Program
Openalex Percentile: Top 24%
Block Copolymer Self-Assembly
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