Polyelectrolyte-mediated interparticle forces in aqueous suspensions: Molecular structure and surface forces relationship

被引:17
|
作者
Leong, Yee-Kwong [1 ]
Ong, Ban-Choon [2 ]
机构
[1] Univ Western Australia, Sch Mech & Chem Engn, Crawley, WA 6009, Australia
[2] Ngee Ann Polytech, Sch Life Sci & Chem Technol, Singapore 599489, Singapore
来源
关键词
Steric; Bridging; Patch charge; Hydrophobic brush; PEI; DIBMA alternating copolymer; OPPOSITELY CHARGED POLYELECTROLYTES; LONG-RANGE ATTRACTION; COLLOIDAL PARTICLES; YIELD-STRESS; ADSORBED POLYELECTROLYTES; HYDROPHOBIC SURFACES; STERIC INTERACTIONS; SILICA DISPERSIONS; FLOCCULATION; POLYMER;
D O I
10.1016/j.cherd.2015.07.001
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
Surface forces in suspensions must be controlled if optimum processing is to be achieved as they govern their processing behaviour. Surface chemistry tools such as pH, ionic strength and adsorbed additives are often used to effect and control these forces. Adsorbed polyelectrolytes give rise to a range of non-DLVO surface forces in colloidal dispersions depending upon their molecular and structural properties. These forces are steric, bridging, patch charge, entropic or "hydrophobic" and others. In this paper these polymer-mediated forces will be discussed in relation to the polymer molecular, structural and physical properties. Scientists, process engineers, metallurgists and related practitioners wishing to optimize the handling/processing of colloidal suspension in the processes employed by their industries may find the experimental and theoretical knowledge, and fundamental principles established in this review paper very beneficial. (C) 2015 The Institution of Chemical Engineers. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:44 / 55
页数:12
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