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dc.contributor.authorChaliha, D.
dc.contributor.authorGomes, J.F.
dc.contributor.authorSmith, P.
dc.contributor.authorJones, Franca
dc.date.accessioned2022-07-20T01:41:40Z
dc.date.available2022-07-20T01:41:40Z
dc.date.issued2022
dc.identifier.citationChaliha, D. and Gomes, J.F. and Smith, P. and Jones, F. 2022. In situ atomic force microscopy (AFM) investigation of kaolinite dissolution in highly caustic environments. CrystEngComm. 24 (11): pp. 2042-2049.
dc.identifier.urihttp://hdl.handle.net/20.500.11937/88970
dc.identifier.doi10.1039/d1ce01572a
dc.description.abstract

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.

dc.languageEnglish
dc.publisherROYAL SOC CHEMISTRY
dc.relation.sponsoredbyhttp://purl.org/au-research/grants/arc/LE130100053
dc.relation.sponsoredbyhttp://purl.org/au-research/grants/arc/LE140100150
dc.relation.sponsoredbyhttp://purl.org/au-research/grants/arc/LE0775551
dc.subjectScience & Technology
dc.subjectPhysical Sciences
dc.subjectChemistry, Multidisciplinary
dc.subjectCrystallography
dc.subjectChemistry
dc.subjectSPENT BAYER LIQUOR
dc.subjectSMECTITE DISSOLUTION
dc.subjectMOLECULAR-DYNAMICS
dc.subjectROOM-TEMPERATURE
dc.subjectMECHANISM
dc.subjectDESILICATION
dc.subjectSODALITE
dc.subjectKINETICS
dc.subjectSOLUBILITY
dc.subjectCANCRINITE
dc.titleIn situ atomic force microscopy (AFM) investigation of kaolinite dissolution in highly caustic environments
dc.typeJournal Article
dcterms.source.volume24
dcterms.source.number11
dcterms.source.startPage2042
dcterms.source.endPage2049
dcterms.source.titleCrystEngComm
dc.date.updated2022-07-20T01:41:35Z
curtin.departmentSchool of Molecular and Life Sciences (MLS)
curtin.accessStatusOpen access
curtin.facultyFaculty of Science and Engineering
curtin.contributor.orcidJones, Franca [0000-0002-8461-8291]
curtin.contributor.researcheridJones, Franca [K-7651-2013]
dcterms.source.eissn1466-8033
curtin.contributor.scopusauthoridJones, Franca [7401454856]


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