Electrophoresis of concentrated colloidal dispersions in low-polar solvents

被引:31
作者
Vissers, Teun [1 ]
Imhof, Arnout [1 ]
Carrique, Felix [2 ]
Delgado, Angel V. [3 ]
van Blaaderen, Alfons [1 ]
机构
[1] Univ Utrecht, Debye Inst Nanomat Sci, NL-3584 CC Utrecht, Netherlands
[2] Univ Malaga, Fac Ciencias, Dept Fis Aplicada 1, E-29071 Malaga, Spain
[3] Univ Granada, Fac Ciencias, Dept Fis Aplicada, E-18071 Granada, Spain
关键词
Colloids; Electrophoresis; Low-polar; Real-space; Zeta-potential; Charge; Self-diffusion; TIME SELF-DIFFUSION; NONAQUEOUS MEDIA; MODEL SYSTEM; HYDRODYNAMIC INTERACTIONS; ELECTROKINETIC PHENOMENA; SPHERICAL-PARTICLES; CHARGED-PARTICLES; VOLUME FRACTION; SUSPENSIONS; MOBILITY;
D O I
10.1016/j.jcis.2011.04.113
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
We present a method to accurately measure the electrophoretic mobility of spherical colloids at high volume fractions in real space using confocal laser scanning microscopy (CLSM) and particle tracking. We show that for polymethylmethacrylate (PMMA) particles in a low-polar, density- and refractive-index-matched mixture of cyclohexylbromide and cis-decahydronaphthalene, the electrophoretic mobility decreases nonlinearly with increasing volume fraction. From the electrophoretic mobilities, we calculate the c-potential and the particle charge with and without correcting for volume fraction effects. For both cases, we find a decreasing particle charge as a function of volume fraction. This is in accordance with the fact that the charges originate from chemical equilibria that represent so-called weak association and/or dissociation reactions. Finally, as our methodology also provides data on particle self-diffusion in the presence of an electric field, we also analyze the diffusion at different volume fractions and identify a nonlinear decreasing trend for increasing volume fraction. (C) 2011 Elsevier Inc. All rights reserved.
引用
收藏
页码:443 / 455
页数:13
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