Anion-specific effects on the interaction forces between Al2O3 surfaces and dispersibility of Al2O3 colloids in electrolyte solutions

被引:5
作者
Isobe, Toshihiro [1 ]
Nakagawa, Yosuke [1 ]
Hayashi, Mikiro [1 ]
Matsushita, Sachiko [1 ]
Nakajima, Akira [1 ]
机构
[1] Tokyo Inst Technol, Dept Met & Ceram Sci, Tokyo, Japan
关键词
Atomic force microscopy; Force curve; DLVO theory; ALUMINA SURFACES; SILICA SURFACES; MICA SURFACES; MICROSCOPE; HYDRATION; CERAMICS; WATER; PH;
D O I
10.1016/j.colsurfa.2011.12.072
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 interaction between an Al2O3 colloid and c-sapphire surface (0001) was investigated in an aqueous solution containing citrate ion, Cl-, NO3- or Br- using the colloidal probe method. The force curve measured in electrolyte solutions at pH = 4 showed a good agreement with the force curve predicted by the Derjaguin-Landau-Vervey-Overbeek theory at a long separation distance. The repulsive forces were observed at a shorter separation distance. The order of the strength of the repulsive force was citrate ion > Cl- > NO3- > Br-, corresponding to the Hofmeister series. All the force curves measured in aqueous solutions at pH = 10 were the same. This is caused by the cation (K+) selectively affecting surface interaction because the Al2O3 surface charged to negative at this pH. A particle size distribution measurement of the Al2O3 colloids in the 0.001-0.1 mol/L Cl- and Br- aqueous solution was carried out. The agglomerates of the Al2O3 colloids were observed in 0.1 mol/L Br- solutions. However, Al2O3 colloids were well dispersed in the other aqueous solutions, which are reflected by the force curve results. Jump-in was observed only in the force curve measured in the 0.1 mol/L Br- solutions and not in any other solutions. Crown Copyright (C) 2012 Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:233 / 237
页数:5
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