Diffusiophoretic mobility of charged porous spheres in electrolyte gradients

JOURNAL OF COLLOID AND INTERFACE SCIENCE

卷:269

Article

Wei, YK ; Keh, HJ

关键词: diffusiophoresis;    polyelectrolyte particles;    charged porous spheres;   

DOI  :  10.1016/j.jcis.2003.08.054

来源: Elsevier

【 摘 要 】

The diffusiophoretic motion of a polyelectrolyte, molecule or charged floc in an unbounded solution of a symmetrically charged electrolyte with a uniform prescribed concentration gradient is analytically studied. The model used for the particle is a porous sphere in which the density of the hydrodynamic frictional segments, and therefore also that of the fixed charges, is constant. The electrokinetic equations which govern the electrostatic potential profile, the ionic concentration distributions (or electrochemical potential energies), and the fluid velocity field inside and outside the porous particle are linearized by assuming that the system is only slightly distorted from equilibrium. Using a regular perturbation method, these linearized equations are solved for a charged porous sphere with the density of the fixed charges as the small perturbation parameter. An analytical expression for the diffusiophoretic mobility of the charged porous sphere in closed form is obtained from a balance between its electrostatic and hydrodynamic forces. This expression, which is correct to the second order of the fixed charge density of the particle, is valid for arbitrary values of kappaa and lambdaa, where kappa is the reciprocal of the Debye screening length, lambda is the reciprocal of the length characterizing the extent of flow penetration inside the particle, and a is the particle radius. Our result to the first order of the fixed charge density agrees with the corresponding solution for the electrophoretic mobility obtained in the literature. In general, the diffusiophoretic mobility of a porous particle becomes greater as the hindrance to the diffusive transport of the solute species inside the particle is more significant. (C) 2003 Elsevier Inc. All rights reserved.

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