Chan Derek Y C, Healy Thomas W, Supasiti Tharatorn, Usui S
Department of Mathematics and Statistics, University of Melbourne, Victoria 3010, Australia.
J Colloid Interface Sci. 2006 Apr 1;296(1):150-8. doi: 10.1016/j.jcis.2005.09.003. Epub 2005 Oct 4.
Models of surfaces with intrinsic ionisable amphoteric surface sites governed by the dissociation of acid-base potential determining ion species together with the capacity for the adsorption of anion and cations of the supporting electrolyte are required to describe both the results of electrokinetic and titration measurements of inorganic oxides. The Gouy-Chapman-Stern-Grahame (CGSG) model is one such model that has been widely used in the literature. The electrical double layer interaction between two dissimilar CGSG surfaces has been studied by Usui recently [S. Usui, J. Colloid Interface Sci. 280 (2004) 113] where erroneous discontinuities in the slope of the pressure-separation relation were observed. We revisit this calculation and provide a simple general methodology to analyse the electrical double layer interaction between dissimilar ionisable surfaces with ion adsorption.
为了描述无机氧化物的电动和滴定测量结果,需要建立具有内在可电离两性表面位点的表面模型,这些位点由酸碱电位决定离子物种的解离以及支持电解质的阴离子和阳离子的吸附能力所控制。古伊-查普曼-斯特恩-格雷厄姆(CGSG)模型就是这样一种在文献中被广泛使用的模型。最近,臼井[S. Usui, J. Colloid Interface Sci. 280 (2004) 113]研究了两个不同的CGSG表面之间的电双层相互作用,其中观察到压力-分离关系斜率存在错误的不连续性。我们重新审视了这一计算,并提供了一种简单的通用方法来分析具有离子吸附的不同可电离表面之间的电双层相互作用。