Electrodiffusiophoresis: Particle motion in electrolytes under direct current
Name
Bazant_Electrodiffusiophoresis particle.pdf
Size
1013.96 KB
Format
Adobe PDF
Checksum (MD5)
af431db4be0def9493a8e5d8421695cd
Author(s) •
Rica, Raul A.
Bazant, Martin Z.
Date Issued
November 2010
Journal
Physics of Fluids
Publisher
American Institute of Physics
Citation
Rica, Raúl A., and Martin Z. Bazant. “Electrodiffusiophoresis: Particle motion in electrolytes under direct current.” Physics of Fluids 22.11 (2010) : 112109. © 2010 American Institute of Physics
Version
Final published version
Abstract
Colloidal particles in electrolytes move in response to electric fields (electrophoresis) and salt concentration gradients (diffusiophoresis), and related flows also occur at fixed surfaces (electro-osmosis and diffusio-osmosis, respectively). In isolation, these electrokinetic phenomena are well understood, e.g., electrophoresis without far-field concentration gradients and diffusiophoresis without applied electric fields. When the electrolyte passes direct current, however, concentration gradients accompany the bulk electric field (concentration polarization) and the resulting particle motion, called “electrodiffusiophoresis,” involves a nonlinear combination of electrophoresis and diffusiophoresis, depending on ion transference numbers and particle properties. In this work, we analyze the electrodiffusiophoresis of spherical particles in the limit of thin double layers, neglecting surface conduction (Du<<1) and convection (Pe<<1), considering both nonpolarizable (fixed charge) and ideally polarizable (induced-charge) surfaces. Via asymptotic approximations and numerical solutions, we develop a physical picture to guide potential applications in electrochemical cells, such as analyte focusing, electrophoretic deposition, and microfluidic mixing near membranes or electrodes. By controlling the mean salt concentration, particle size, current, and concentration gradient, significant motion of particles (or fluid) is possible toward either electrode and toward high or low concentration.
MIT Department
Massachusetts Institute of Technology. Department of Chemical Engineering
Massachusetts Institute of Technology. Department of Mathematics
Terms of Use
Article is made available in accordance with the publisher's policy and may be subject to US copyright law. Please refer to the publisher's site for terms of use.
Persistent DSpace Link
DOI of Published Version
https://doi.org/10.1063/1.3496976