Abstract
The motion of a spherical particle undergoing electrophoresis in weakly inertial or viscoelastic shear flow is quantified via asymptotic analysis. We are motivated by several experimental studies reporting cross-streamline migration of electrophoretic colloids in Poiseuille microchannel flow. Specifically, particles migrate in a Newtonian liquid to the center (walls) of a channel when their electrophoretic velocity is in the opposite (same) direction to (as) the flow. Here, we calculate that weak fluid inertia causes a leading-order cross-streamline lift force of magnitude for electrophoresis along the velocity axis of an unbounded simple shear flow, where and denote the particle zeta potential and radius, respectively; , , and are the fluid density, viscosity, and permittivity, respectively; is the shear rate of the ambient flow; and is the strength of the imposed electric field. This force acts to propel the sphere to shear streamlines that, in a frame translating with the particle, are directed reverse to the electrophoretic motion, which is consistent with the above-mentioned experiments. Other recent experiments have observed migration of electrophoretic particles in Poiseuille flow of a viscoelastic polymer solution: the migration direction is opposite to that in a Newtonian liquid. Here, we calculate a leading-order cross-streamline lift force of magnitude for electrophoresis in simple shear flow of a second-order fluid, where and are the first and second normal stress coefficients, respectively. The lift is toward streamlines moving in the direction of electrophoresis for (a reasonable assumption for polymeric liquids, where and are negative and positive, respectively), which is consistent with the experiments. Finally, an estimation of the magnitude of the lift forces and associated drift velocities further suggests that the cumulative effect of weak instantaneous inertia or viscoelasticity is responsible, or at least contributes appreciably, to the observed migration.
- Received 11 July 2019
- Accepted 19 February 2020
DOI:https://doi.org/10.1103/PhysRevFluids.5.033702
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