'Exact' solutions of the full electrokinetic model for soft spherical colloids: Electrophoretic mobility

被引:92
作者
Hill, RJ [1 ]
Saville, DA
机构
[1] McGill Univ, Dept Chem Engn, 3640 Univ St, Montreal, PQ H3A 2B2, Canada
[2] McGill Univ, McGill Inst Adv Mat, Montreal, PQ H3A 2B2, Canada
[3] Princeton Univ, Dept Chem Engn, Princeton, NJ 08542 USA
关键词
electrophoretic mobility; electrokinetic phenomena; soft colloids; polymer-coated colloids; sterically stabilized colloids; stealth liposomes; human erythrocytes; charged micelles;
D O I
10.1016/j.colsurfa.2005.06.035
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
Numerical solutions of the standard electrokinetic model provide a basis for interpreting a variety of electrokinetic phenomena involving 'bare' colloids. However, the model rests on the classical notion of a shear or slipping plane, whose location is unknown when surfaces are coated with permeable polymer. Consequently, an electrokinetic model for 'soft', 'hairy' or 'fuzzy' colloids has been developed, but until recently solutions were available only for several restricted cases, most notably for particles with thin, uniform layers, and without polarization and relaxation. Here we present numerically exact solutions of the full model for a variety of soft colloids, including PEG-coated liposomes, PEO-coated latices, human erythrocytes, and polyelectrolyte micelles. Particular attention is given to linking the thickness, density and permeability of the coatings, which are key parameters in the model, to "physical" quantities, such as the polymer molecular weight, adsorbed amount, and hydrodynamic layer thickness. This paper also identifies limits - on the ionic strength, particle size, layer thickness and permeability - beyond which earlier theories breakdown. In short, polarization and relaxation are as influential on the mobility of soft colloids as they are for 'bare' particles. (c) 2005 Elsevier B.V. All rights reserved.
引用
收藏
页码:31 / 49
页数:19
相关论文
共 28 条
[1]  
Anderson JL, 1996, CHEM ENG COMMUN, V150, P291
[2]   Ionizable polyelectrolyte brushes: brush height and electrosteric interaction [J].
Biesheuvel, PM .
JOURNAL OF COLLOID AND INTERFACE SCIENCE, 2004, 275 (01) :97-106
[3]   Electrokinetic measurement of hydrodynamic properties of grafted polymer layers on liposome surfaces [J].
Cohen, JA ;
Khorosheva, VA .
COLLOIDS AND SURFACES A-PHYSICOCHEMICAL AND ENGINEERING ASPECTS, 2001, 195 (1-3) :113-127
[4]   Capillary electrophoresis of associative diblock copolymers [J].
Cottet, H ;
Gareil, P ;
Guenoun, P ;
Muller, F ;
Delsanti, M ;
Lixon, P ;
Mays, JW ;
Yang, J .
JOURNAL OF CHROMATOGRAPHY A, 2001, 939 (1-2) :109-121
[5]  
DUKHIN SS, 1970, KOLLOID ZH, V32, P360
[6]   Analytical approximation to the Scheutjens-Fleer theory for polymer adsorption from dilute solution. 2. Adsorbed amounts and structure of the adsorbed layer [J].
Fleer, GJ ;
van Male, J ;
Johner, A .
MACROMOLECULES, 1999, 32 (03) :845-862
[7]  
FLEER GJ, 1988, POLYM INTERFACES
[8]   Electrophoretic behavior of bare and polymer-coated latices [J].
Gittings, MR ;
Saville, DA .
LANGMUIR, 2000, 16 (16) :6416-6421
[9]   Ionic strength and curvature effects in flat and highly curved polyelectrolyte brushes [J].
Hariharan, R ;
Biver, C ;
Mays, J ;
Russel, WB .
MACROMOLECULES, 1998, 31 (21) :7506-7513
[10]  
Hermans J. J., 1955, P K NED AKAD B PHYS, V58, P182