Colloid stability and electrokinetic characterization of polymer colloids prepared by different methods

被引:32
作者
PeulaGarcia, JM
Hidalgo-Alvarez, R
delasNieves, FJ
机构
[1] UNIV ALMERIA, DEPT APPL PHYS, COMPLEX FLUIDS PHYS GRP, ALMERIA 04120, SPAIN
[2] UNIV GRANADA, DEPT APPL PHYS, BIOCOLLOIDS & FLUIDS PHYS GRP, E-18071 GRANADA, SPAIN
关键词
colloid stability; electrosteric stabilization; sulfonated polystyrene latexes;
D O I
10.1016/S0927-7757(96)03890-3
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
The electrokinetic characterization and colloidal stability of functionalized latexes, two sulfonated polystyrene model colloids prepared by different methods, are described. JM1 latex was synthesized by an emulsion copolymerization process from styrene and sodium styrene sulfonate (NaSS) in the absence of an emulsifier. SN9 latex was prepared by a two-stage ''shot-growth'' emulsion polymerization process without emulsifier and using NaSS as an ionic comonomer. The two latexes had nearly the same particle size but very different surface charge densities. When the electrophoretic mobility of these functionalized model colloids was studied as a function of pH and ionic strength, the latex with the lower surface charge yielded higher mobility values. The experimental results for the electrokinetic characterization suggest that the surface of the particles prepared with a second injection is covered by a layer of oligomers or polymer chains which shift the shear plane towards the bulk solution, increasing the anomalous surface conductance of the particle-electrolyte solution interface. The stability factor and the critical coagulation concentration were studied for the two samples. Better colloidal stability was observed for the latex prepared with the second injection, which has a higher surface charge density. There is an important electrostatic contribution to the stability, but there also seems to be a steric contribution due to the structure of the electric double layer which surrounds the particles. (C) 1997 Elsevier Science B.V.
引用
收藏
页码:19 / 24
页数:6
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