In situ atomic force microscopy (AFM) investigation of kaolinite dissolution in highly caustic environments

Clays are a common component of bauxite, and reactive silica, in the form of clays, is an important precursor of desilication products. Despite this, the behaviour of clays in highly caustic environments is not well investigated and this is due to the nature of the corrosive environment as well as t...

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Main Authors: Chaliha, D., Gomes, J.F., Smith, P., Jones, Franca
Format: Journal Article
Language:English
Published: ROYAL SOC CHEMISTRY 2022
Subjects:
Online Access:http://purl.org/au-research/grants/arc/LE130100053
http://hdl.handle.net/20.500.11937/88970
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author Chaliha, D.
Gomes, J.F.
Smith, P.
Jones, Franca
author_facet Chaliha, D.
Gomes, J.F.
Smith, P.
Jones, Franca
author_sort Chaliha, D.
building Curtin Institutional Repository
collection Online Access
description Clays are a common component of bauxite, and reactive silica, in the form of clays, is an important precursor of desilication products. Despite this, the behaviour of clays in highly caustic environments is not well investigated and this is due to the nature of the corrosive environment as well as the temperatures normally encountered (normally ∼90 °C for the desilication process unit). Atomic force microscopy has been used in this work to image the dissolution of kaolinite in situ at various temperatures (25-55 °C) and in different solutions (pure caustic, synthetic Bayer liquor and synthetic Bayer liquor with added waterglass). This work has shown that the dissolution behaviour is similar in all these solutions. Little impact of temperature is expected on dissolved silicate in the range studied though some of the results may be impacted by the batch nature of the set-up. In the synthetic Bayer liquor, due to the aluminate present, it can also be concluded that the aluminate sheet of the kaolinite should dissolve more slowly than the silicate sheet. The dissolution of kaolinite steps in the Bayer liquor is slightly faster compared to the pure caustic case. In addition, there is a fast and slow dissolution direction for the steps observed on kaolinite. However, the size of the particles or features also changes suggesting that edges are the fastest features to dissolve and this is supported by the initial formation of aluminosilicates at kaolinite edges.
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spelling curtin-20.500.11937-889702023-03-20T03:38:33Z In situ atomic force microscopy (AFM) investigation of kaolinite dissolution in highly caustic environments Chaliha, D. Gomes, J.F. Smith, P. Jones, Franca Science & Technology Physical Sciences Chemistry, Multidisciplinary Crystallography Chemistry SPENT BAYER LIQUOR SMECTITE DISSOLUTION MOLECULAR-DYNAMICS ROOM-TEMPERATURE MECHANISM DESILICATION SODALITE KINETICS SOLUBILITY CANCRINITE Clays are a common component of bauxite, and reactive silica, in the form of clays, is an important precursor of desilication products. Despite this, the behaviour of clays in highly caustic environments is not well investigated and this is due to the nature of the corrosive environment as well as the temperatures normally encountered (normally ∼90 °C for the desilication process unit). Atomic force microscopy has been used in this work to image the dissolution of kaolinite in situ at various temperatures (25-55 °C) and in different solutions (pure caustic, synthetic Bayer liquor and synthetic Bayer liquor with added waterglass). This work has shown that the dissolution behaviour is similar in all these solutions. Little impact of temperature is expected on dissolved silicate in the range studied though some of the results may be impacted by the batch nature of the set-up. In the synthetic Bayer liquor, due to the aluminate present, it can also be concluded that the aluminate sheet of the kaolinite should dissolve more slowly than the silicate sheet. The dissolution of kaolinite steps in the Bayer liquor is slightly faster compared to the pure caustic case. In addition, there is a fast and slow dissolution direction for the steps observed on kaolinite. However, the size of the particles or features also changes suggesting that edges are the fastest features to dissolve and this is supported by the initial formation of aluminosilicates at kaolinite edges. 2022 Journal Article http://hdl.handle.net/20.500.11937/88970 10.1039/d1ce01572a English http://purl.org/au-research/grants/arc/LE130100053 http://purl.org/au-research/grants/arc/LE140100150 http://purl.org/au-research/grants/arc/LE0775551 ROYAL SOC CHEMISTRY fulltext
spellingShingle Science & Technology
Physical Sciences
Chemistry, Multidisciplinary
Crystallography
Chemistry
SPENT BAYER LIQUOR
SMECTITE DISSOLUTION
MOLECULAR-DYNAMICS
ROOM-TEMPERATURE
MECHANISM
DESILICATION
SODALITE
KINETICS
SOLUBILITY
CANCRINITE
Chaliha, D.
Gomes, J.F.
Smith, P.
Jones, Franca
In situ atomic force microscopy (AFM) investigation of kaolinite dissolution in highly caustic environments
title In situ atomic force microscopy (AFM) investigation of kaolinite dissolution in highly caustic environments
title_full In situ atomic force microscopy (AFM) investigation of kaolinite dissolution in highly caustic environments
title_fullStr In situ atomic force microscopy (AFM) investigation of kaolinite dissolution in highly caustic environments
title_full_unstemmed In situ atomic force microscopy (AFM) investigation of kaolinite dissolution in highly caustic environments
title_short In situ atomic force microscopy (AFM) investigation of kaolinite dissolution in highly caustic environments
title_sort in situ atomic force microscopy (afm) investigation of kaolinite dissolution in highly caustic environments
topic Science & Technology
Physical Sciences
Chemistry, Multidisciplinary
Crystallography
Chemistry
SPENT BAYER LIQUOR
SMECTITE DISSOLUTION
MOLECULAR-DYNAMICS
ROOM-TEMPERATURE
MECHANISM
DESILICATION
SODALITE
KINETICS
SOLUBILITY
CANCRINITE
url http://purl.org/au-research/grants/arc/LE130100053
http://purl.org/au-research/grants/arc/LE130100053
http://purl.org/au-research/grants/arc/LE130100053
http://hdl.handle.net/20.500.11937/88970