Chun B, Ladd A J C
Department of Chemical Engineering, University of Florida, Gainesville, FL 32611-6005, USA.
J Colloid Interface Sci. 2004 Jun 15;274(2):687-94. doi: 10.1016/j.jcis.2004.03.066.
We have investigated the hydrodynamic drag force between charged particles in electrolyte solutions, specifically the electroviscous force that arises from the distortion of the electrical double layers by the flow field. We report an improvement on the thin-double-layer theory (S.G. Bike, D.C. Prieve, J. Colloid Interface Sci. 136 (1990) 95-112), using a more accurate boundary condition for the radial charge current. The differences become important when the double layers start to overlap. We have found that nonlinear hydrodynamic effects are small, whereas nonlinear electric effects can be significant, in some instances leading to qualitatively different behavior. If the ion diffusivities are highly asymmetric, the electroviscous force can be reduced by an order of magnitude when there is an excess of the mobile ions in the double layer. The common supposition that there are substantial differences in the electroviscous force predicted by constant-charge and constant-potential boundary conditions is incorrect; our calculations show that it is an artifact introduced by the Debye-Hückel approximation.
我们研究了电解质溶液中带电粒子之间的流体动力学阻力,特别是由流场导致的电双层畸变所产生的电黏滞力。我们报告了对薄双层理论(S.G. 比克、D.C. 普里夫,《胶体与界面科学杂志》136 (1990) 95 - 112)的改进,采用了更精确的径向电荷电流边界条件。当双层开始重叠时,这些差异变得很重要。我们发现非线性流体动力学效应很小,而非线性电效应可能很显著,在某些情况下会导致定性不同的行为。如果离子扩散率高度不对称,当双层中存在过量的可移动离子时,电黏滞力可降低一个数量级。认为恒定电荷和恒定电位边界条件所预测的电黏滞力存在实质性差异的常见假设是不正确的;我们的计算表明这是德拜 - 休克尔近似引入的假象。