The influence of interfacial structuring on gibbsite interactions in synthetic Bayer liquors

被引:31
作者
Addai-Mensah, J [1 ]
Ralston, J [1 ]
机构
[1] Univ S Australia, Ian Wark Res Inst, Adelaide, SA 5095, Australia
基金
澳大利亚研究理事会;
关键词
Bayer liquor; steric forces; adhesive forces; gibbsite agglomeration; crystallization;
D O I
10.1006/jcis.1999.6237
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 forces between gibbsite particles aging in synthetic, supersaturated sodium and potassium aluminate solutions (Bayer liquors) have been investigated. Compliance with DLVO-type behavior was observed in dilute electrolyte. Under synthetic Bayer conditions, non-DLVO, repulsive steric forces exist. Upon aging, this steric repulsion gradually diminishes and disappears. A structured interfacial layer, displaying inner and outer regions of different compressibility, develops as aging occurs and interparticle adhesion increases. At high particle approach velocities, hydrodynamic forces exist which are dependent upon the viscosity of solution. The steric, adhesive, and hydrodynamic interactions are all greater in NaAl(OH)(4) compared with KAl(OH)(4) liquors of the same concentrations and degree of aging. Solution AI(OH)(4)(-) ion-mediated interfacial structuring is apparently responsible for the time-dependent repulsive and adhesive forces. These interfacial phenomena are perceived to be precursors to, or part of, gibbsite crystal growth and agglomeration mechanisms. (C) 1999 Academic Press.
引用
收藏
页码:124 / 130
页数:7
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