2022
DOI: 10.1016/j.jcis.2022.08.084
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Hydrodynamic interactions between charged and uncharged Brownian colloids at a fluid-fluid interface

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Cited by 4 publications
(4 citation statements)
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“…The properties of particle-laden layers at the equilibrium depend on the nature of the interface, the particle-interface interactions, and inter-particle interactions. To predict the adsorption equilibrium, one should take into account the van der Waals and electrostatic interactions between all species, the interactions induced by the interface, such as the electrical double layer forces, capillary interactions, hydrodynamic interactions [62], and sometimes, also, externally actuated interactions. The interactions can be additionally modulated by the environmental conditions, for example pH, ionic strength, or temperature.…”
Section: Chemically Homogeneous Particles At Fluid-fluid Interfaces 2...mentioning
confidence: 99%
See 1 more Smart Citation
“…The properties of particle-laden layers at the equilibrium depend on the nature of the interface, the particle-interface interactions, and inter-particle interactions. To predict the adsorption equilibrium, one should take into account the van der Waals and electrostatic interactions between all species, the interactions induced by the interface, such as the electrical double layer forces, capillary interactions, hydrodynamic interactions [62], and sometimes, also, externally actuated interactions. The interactions can be additionally modulated by the environmental conditions, for example pH, ionic strength, or temperature.…”
Section: Chemically Homogeneous Particles At Fluid-fluid Interfaces 2...mentioning
confidence: 99%
“…As a result, the shape of the particle changes, which in turn affects its ability to be trapped in the interface. Thus, the temperature is the important parameter controlling the adsorption of hairy particles on fluid-fluid interfaces [62].…”
Section: Individual Hairy Particles At Fluid-fluid Interfacesmentioning
confidence: 99%
“…We simply treat the medium fluid as a bulk with constant viscosity η and use the fast Stokesian dynamics method described in ( 38 ) to account for hydrodynamic interactions between particles. This approximation is reasonable because the particles that we consider are jammed on the droplet interface and do not move much relative to each other, rendering interfacial corrections to the hydrodynamic mobility higher order ( 39 , 40 ). Furthermore, the literature has shown that even with the full resolution of a two-phase Stokesian fluid, corrections to the bulk hydrodynamic mobility are typically less than 10% ( 41 ).…”
Section: Methodsmentioning
confidence: 99%
“…While reports are available in the literature on the impacts of various particle attributes on the resulting interfacial microstructure at the air–water interface [ 31 , 32 , 33 , 34 , 41 , 42 , 47 , 48 , 49 , 50 , 51 ], understanding how the particle characteristics affect the resulting interparticle interactions and how to exploit these attributes in engineering the rheological properties of such interfacial particle network is an active area of research [ 52 , 53 ]. Moreover, the potential environmental concerns associated with some nanoparticles are driving a shift towards the use of larger particles in applications [ 54 ].…”
Section: Introductionmentioning
confidence: 99%