Tu HJ, Keh HJ
Department of Chemical Engineering, National Taiwan University, Taipei, Taiwan, 106-17, R.O.C.
J Colloid Interface Sci. 2000 Nov 15;231(2):265-282. doi: 10.1006/jcis.2000.7145.
The diffusiophoretic and electrophoretic motions of two colloidal spheres in the solution of a symmetrically charged electrolyte are analyzed using a method of reflections. The particles are oriented arbitrarily with respect to the electrolyte gradient or the electric field, and they are allowed to differ in radius and in zeta potential. The thickness of the electric double layers surrounding the particles is assumed to be small relative to the radius of each particle and to the gap width between the particles, but the effect of polarization of the mobile ions in the diffuse layer is taken into account. A slip velocity of fluid and normal fluxes of solute ions at the outer edge of the thin double layer are used as the boundary conditions for the fluid phase outside the double layers. The method of reflections is based on an analysis of the electrochemical potential and fluid velocity disturbances produced by a single dielectric sphere placed in an arbitrarily varying electrolyte gradient or electric field. The solution for two-sphere interactions is obtained in expansion form correct to O(r(12)(-7)), where r(12) is the distance between the particle centers. Our analytical results are found to be in good agreement with the available numerical solutions obtained using a boundary collocation method. On the basis of a model of statistical mechanics, the results of two-sphere interactions are used to analytically determine the first-order effect of the volume fraction of particles of each type on the mean diffusiophoretic and eletrophoretic velocities in a bounded suspension. For a suspension of identical spheres, the mean diffusiophoretic velocity can be decreased or increased as the volume fraction of the particles is increased, while the mean electrophoretic velocity is reduced with the increase in the particle concentration. Generally speaking, the particle interaction effects can be quite significant in typical situations. Copyright 2000 Academic Press.
利用反射法分析了两个胶体球在对称带电电解质溶液中的扩散电泳和电泳运动。粒子相对于电解质梯度或电场任意取向,并且允许它们在半径和ζ电位上有所不同。假设围绕粒子的双电层厚度相对于每个粒子的半径和粒子之间的间隙宽度较小,但考虑了扩散层中移动离子的极化效应。将流体的滑移速度和薄双电层外边缘处溶质离子的法向通量用作双电层外流体相的边界条件。反射法基于对置于任意变化的电解质梯度或电场中的单个介电球产生的电化学势和流体速度扰动的分析。得到了两球相互作用的展开形式解,精确到O(r(12)(-7)),其中r(12)是粒子中心之间的距离。我们的分析结果与使用边界配置法获得的现有数值解非常吻合。基于统计力学模型,利用两球相互作用的结果来解析确定每种类型粒子的体积分数对有限悬浮液中平均扩散电泳速度和电泳速度的一级效应。对于相同球体的悬浮液,随着粒子体积分数的增加,平均扩散电泳速度可能降低或增加,而平均电泳速度随着粒子浓度的增加而降低。一般来说,在典型情况下,粒子相互作用效应可能相当显著。版权所有2000年学术出版社。