Origins of the non-DLVO force between glass surfaces in aqueous solution

被引:81
|
作者
Adler, JJ [1 ]
Rabinovich, YI [1 ]
Moudgil, BM [1 ]
机构
[1] Univ Florida, Dept Mat Sci & Engn, Engn Res Ctr Particle Sci & Technol, Gainesville, FL 32611 USA
基金
美国国家科学基金会;
关键词
structural force; hydration force; non-DLVO; atomic force microscope; silica; glass; gel; silicic acid; transition layer; van der Waals;
D O I
10.1006/jcis.2001.7466
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
Direct measurement of surface forces has revealed that silica surfaces seem to have a short-range repulsion that is not accounted for in classical DLVO theory. The two leading hypotheses for the origin of the non-DLVO force are (i) structuring of water at the silica interface or (ii) water penetration into the surface resulting in a gel layer. In this article, the interaction of silica surfaces will be reviewed from the perspective of the non-DLVO force origin. In an attempt to more accurately describe the behavior of silica and glass surfaces, alternative models of how surfaces with gel layers should interact are proposed. It is suggested that a lessened van der Waals attraction originating from a thin gel layer may explain both the additional stability and the coagulation behavior of silica. It is important to understand the mechanisms underlying the existence of the non-DLVO force which is likely to have a major influence on the adsorption of polymers and surfactants used to modify the silica surface for practical applications in the ceramic, mineral, and microelectronic industries. (C) 2001 Academic Press.
引用
收藏
页码:249 / 258
页数:10
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