Hydrodynamic Interactions Between Charged and Uncharged Brownian Colloids at a Fluid-Fluid Interface
Archit Dani, Mohsen Yeganeh, Charles Maldarelli

TL;DR
This study uses Langevin dynamic simulations to explore how hydrodynamic interactions and thermal fluctuations influence the self-assembly of charged and uncharged colloids at a fluid-fluid interface, revealing conditions for clustering and ordering.
Contribution
It introduces a detailed simulation framework that accounts for hydrodynamic interactions, electrostatic forces, and thermal fluctuations at fluid interfaces, advancing understanding of colloidal self-assembly.
Findings
Clustering and ordered structures occur at high Pe numbers.
Lower Pe numbers lead to uncorrelated, widely separated particles.
Hydrodynamic interactions significantly influence particle assembly behavior.
Abstract
Hypothesis: The collective dynamics and self-assembly of colloids floating at a fluid/fluid interface is a balance between deterministic lateral interaction forces, viscous resistance to colloid motion along the surface and thermal (Brownian) fluctuations. As the colloid size decreases, thermal forces become important and can affect the self assembly into ordered patterns and crystal structures that are the starting point for various materials applications. Numerics: Langevin dynamic simulations involving two particles straddling a liquid/liquid interface with a high viscosity contrast are presented to describe the lateral interfacial assembly of particles in Brownian and non-Brownian dominated regimes. These simulations incorporate capillary attraction, electrostatic repulsion, thermal fluctuations and HI between particles (including the effect of the particle immersion depth).…
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Taxonomy
TopicsPickering emulsions and particle stabilization
