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YC Kuo

Publications and source records attributed to YC Kuo.

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Dynamic Interactions of Two Electrical Double Layers

The unsteady-state electrical potential and the concentrations of ions between two identical, negatively-charged particles immersed in an a:b electrolyte solution are investigated. In particular, the effects of ionic strength, I, the geometric mean of the diffusivities of counterions Dcon and coions Dco, D, the separation distance between two particles, H, and the surface charge density, sigma0, on these distributions are examined. We conclude that under the following conditions a system needs a longer time for ions to reach equilibrium distributions: (a) small I, (b) small D, (c) large H, and (d) large sigma0. The rate of approach of two particles is faster if both surfaces are maintained at constant potential than if both surfaces are at constant charge density. The dynamic behavior of the relaxation of ions in the double layers has the effect of retarding the motion of particles. The deviation in the contact time between two particles predicted by an equilibrium model, which assumes that the distributions of ions in a double layer reach the Boltzmann distribution instantly, from that estimated by the corresponding dynamic model is on the order of 10%. Copyright 1997 Academic Press. Copyright 1997Academic Press

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The Critical Coagulation Concentration of Counterions: Spherical Particles in Asymmetric Electrolyte Solutions

The ratio of the critical coagulation concentration (CCC) of counterions is evaluated for spherical particles and asymmetric electrolytes. A perturbation method is adopted to solve the Poisson-Boltzmann equation governing the electrical potential distribution of the system under consideration. On the basis of the result obtained, an approximate expression for the CCC is derived. Another approach based on the Derjaguin approximation is also used to estimate the CCC. We show that the CCC ratio of counterions is a complicated function of the valences of the ion species in the liquid phase and the sizes of particles. Depending upon the thickness of the Debye length, the CCC ratio of counterions for various combinations of electrolytes can be estimated. The classic Schulze-Hardy rule for planar particles in a symmetric electrolyte solution can be recovered as a limiting case of the present model. If the surface potential is low, the effect of curvature on the CCC ratio of counterions is negligible.

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