2002•Developments in Chemical Engineering and Mineral ProcessingRequires access

Aggregation Behaviour of Gibbsite Crystals in Supersaturated Sodium and Potassium Aluminate Liquors

Jonas Addai‐Mensah, Jun Li, Clive A. Prestidge

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Abstract

Abstract The aggregation behaviour of colloidal size gibbsite crystals in synthetic supersaturated caustic aluminate liquors has been investigated as a function of solution alkali metal ion type and Al(III) relative supersaturation in crystallization studies. The results indicate that alkali metal ions (Na+ versus K+) and supersaturation play an influential role in the particle aggregation mechanism. The initial particle aggregation rate is linearly dependent upon Al(III) relative supersaturation, and is significantly greater in Na+ rather than in K+ based suspensions. The study demonstrates that the initial orthokinetic aggregation and subsequent cementation both lead to faster agglomeration in sodium than in potassium aluminate liquors

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Abstract The aggregation behaviour of colloidal size gibbsite crystals in synthetic supersaturated caustic aluminate liquors has been investigated as a function of solution alkali metal ion type and Al(III) relative supersaturation in crystallization studies. The results indicate that alkali metal ions (Na+ versus K+) and supersaturation play an influential role in the particle aggregation mechanism. The initial particle aggregation rate is linearly dependent upon Al(III) relative supersaturation, and is significantly greater in Na+ rather than in K+ based suspensions. The study demonstrates that the initial orthokinetic aggregation and subsequent cementation both lead to faster agglomeration in sodium than in potassium aluminate liquors

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Abstract The aggregation behaviour of colloidal size gibbsite crystals in synthetic supersaturated caustic aluminate liquors has been investigated as a function of solution alkali metal ion type and Al(III) relative supersaturation in crystallization studies. The results indicate that alkali metal ions (Na+ versus K+) and supersaturation play an influential role in the particle aggregation mechanism. The initial particle aggregation rate is linearly dependent upon Al(III) relative supersaturation, and is significantly greater in Na+ rather than in K+ based suspensions. The study demonstrates that the initial orthokinetic aggregation and subsequent cementation both lead to faster agglomeration in sodium than in potassium aluminate liquors

Key concepts: Supersaturation, Sodium aluminate, Gibbsite, Chemistry, Alkali metal, Potassium, Crystallization, Aluminate

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