Streaming Potential and Associated Electrokinetic Effects through a Channel Filled with Electrolyte Solution Surrounded by a Layer of Immiscible and Dielectric Liquid.

The present article deals with the streaming potential-mediated pressure-driven flow across a channel in which the electrolyte solution is surrounded by a layer of cell membrane. Such a membrane of a biological cell may be modeled as an immiscible and dielectric liquid, which may bear free lipid molecules or charged surfactants. The presence of such additional charged molecules may lead to formation of liquid-liquid interfacial charge. In addition, the dielectric gradient-mediated ion partitioning effect further plays an important role in two-phase electrokinetic motion. We aim to study the generation of streaming potential and electrokinetic conversion efficiency as well as associated electroviscous effect for the undertaken problem. The mathematical model is based on the Poisson-Boltzmann equation for electrostatic potential and the Stokes equation for fluid flow, and the problem is studied considering suitable interfacial conditions for the flow variables along the liquid-liquid interface. The explicit analytical results for velocity and streaming field, electrokinetic energy conversion efficiency, and the parameter indicating the electroviscous effect are derived under the Donnan limit and within the Debye-Hückel electrostatic framework. We further numerically calculated the aforementioned intrinsic electrokinetic parameter associated with the problem undertaken for a wide range of pertinent parameters. The results are illustrated to indicate the impact of pertinent parameters on the generation of the streaming potential and associated electrokinetic effects.

Electrokinetics of Concentrated Suspension of Soft Particles with pH-Regulated Volumetric Charges.

This article presents a theoretical study on the electrokinetics of concentrated suspension of charge-regulated soft particles under a weak electric field and low potential assumptions. The inner core of the undertaken particle is "semisoft" in nature, which allows ion penetration while the fluid cannot flow within it, and the outer soft polymeric shell allows the flow of the ionized fluid. In addition, the inner core and the outer polyelectrolyte layer (PEL) bear pH-regulated basic and acidic functional groups, respectively. The Poisson-Boltzmann equation-based mathematical model was adopted here for electric potential. The fluid flow across the electrolyte medium and PEL is governed by the Stokes equation and the Darcy-Brinkman equation, respectively. The Kuwabara's unit cell model (J. Phys. Soc. Japan, 1959, 14, 522-527) was invoked to observe the effect of the interaction between the neighboring particles in a concentrated suspension. A first order perturbation technique was used to determine the mean electrophoretic mobility of the undertaken soft particles in a concentrated suspension. The effect of pH and concentration of bulk electrolyte, electrohydrodynamic properties of both the inner core and PEL, on the mean electrophoretic mobility has been studied extensively. In addition, the results have been presented for the neutralization factor that measures the fraction of fixed charges neutralized by the mobile counterions.

Electrophoresis of dielectric and immiscible-liquid-layer-encapsulated colloids in aqueous media.

In this paper we consider the electrophoresis of a functionalized nanoparticle in electrolyte solution. The undertaken particle is comprised of a rigid inner core encapsulated with a layer of dielectric liquid (e.g., oil or lipid layer), which is immiscible to the bulk aqueous medium. The peripheral liquid layer of the undertaken nanoparticle contains mobile charges due to presence of solubilized surfactants. The mobile electrolyte ions can penetrate across the peripheral layer depending on the difference in the Born energy of the both phases. Such types of nanoparticles have received substantial attention due to their widespread applications in biomedical research. The electric double layer (EDL) is governed by the linearized Poisson-Boltzmann equation under a low potential limit and the electroosmotic flow field is governed by modified Stokes equation. We adopt the flat-plate formalism to obtain the closed analytical expression for the electrophoretic mobility of the undertaken particle under a thin EDL approximation. The dependence of electrophoretic mobility on the pertinent parameters is also illustrated.

Impact of ion-steric and ion-partitioning effects on electrophoresis of soft particles.

A theoretical study on the electrophoresis of a soft particle is made by taking into account the ion steric interactions and ion partitioning effects under a thin Debye layer consideration with negligible surface conduction. Objective of this study is to provide a simple expression for the mobility of a soft particle which accounts for the finite-ion-size effect and the ion partitioning arise due to the Born energy difference between two media. The Donnan potential in the soft layer is determined by considering the ion steric interactions and the ion partitioning effect. The volume exclusion due to the finite ion size is considered by the Carnahan-Starling equation and the ion partitioning is accounted through the difference in Born energy. The modified Poisson-Boltzmann equation coupled with Stokes-Darcy-Brinkman equations are considered to determine the mobility. A closed-form expression for the electrophoretic mobility is obtained, which reduces to several existing expressions for mobility under various limiting cases.

Importance of core electrostatic properties on the electrophoresis of a soft particle.

The impact of the volumetric charged density of the dielectric rigid core on the electrophoresis of a soft particle is analyzed numerically. The volume charge density of the inner core of a soft particle can arise for a dendrimer structure or bacteriophage MS2. We consider the electrokinetic model based on the conservation principles, thus no conditions for Debye length or applied electric field is imposed. The fluid flow equations are coupled with the ion transport equations and the equation for the electric field. The occurrence of the induced nonuniform surface charge density on the outer surface of the inner core leads to a situation different from the existing analysis of a soft particle electrophoresis. The impact of this induced surface charge density together with the double-layer polarization and relaxation due to ion convection and electromigration is analyzed. The dielectric permittivity and the charge density of the core have a significant impact on the particle electrophoresis when the Debye length is in the order of the particle size. We find that by varying the ionic concentration of the electrolyte, the particle can exhibit reversal in its electrophoretic velocity. The role of the polymer layer softness parameter is addressed in the present analysis.

Numerical study of the influence of solid polarization on electrophoresis at finite Debye thickness.

The influence of solid polarization on the electrophoresis of a uniformly charged dielectric particle for finite values of the particle-to-fluid dielectric permittivity ratio is analyzed quantitatively without imposing the thin Debye length or weak-field assumption. Present analysis is based on the computation of the coupled Poisson-Nernst-Planck and Stokes equations in the fluid domain along with the Laplace equation within the solid. The electrophoretic velocity is determined through the balance of forces acting on the particle. The solid polarization of the charged particle produces a reduction on its electrophoretic velocity compared to a nonpolarizable particle of the same surface charge density. In accordance with the existing thin-layer analysis, our computed results for thin Debye layer shows that the solid polarization is important only when the applied electric field is strong. When the Debye length is in the order of the particle size, the electrophoretic velocity decreases with the rise of the particle permittivity and attains a saturation limit at large values of the permittivity. Our computed solution for electrophoretic velocity is in agreement with the existing asymptotic analyses based on a thin Debye layer for limiting cases.