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Synthesis of kaolinite from micas and K-depleted micas

Published online by Cambridge University Press:  01 January 2024

Yunchul Cho  and
Sridhar Komarneni
Yunchul Cho
Affiliation:
Department of Crop and Soil Sciences and Materials Research Institute, The Pennsylvania State University, University Park, Pennsylvania 16802, USA
Sridhar Komarneni*
Affiliation:
Department of Crop and Soil Sciences and Materials Research Institute, The Pennsylvania State University, University Park, Pennsylvania 16802, USA
*
*E-mail address of corresponding author: [email protected]
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Abstract

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The weathering stages of K-depleted biotite, K-depleted phlogopite, and natural biotite were investigated using hydrothermal treatment with A1C13 solution at 200°C for 12 to 72 h. Although there were some differences in the degree of weathering of the two K-depleted micas, both first transformed to hydroxy-Al interlayered vermiculite (HIV), which then altered to kaolinite. In case of the natural biotite, the biotite first transformed to a K-depleted mica-like phase, which then altered to kaolinite. The natural biotite had resisted weathering to kaolinite more than did the K-depleted biotite, as expected. The K-depleted phlogopite had less resistance in weathering to kaolinite than the K-depleted biotite. The transformation process changed the color of the micas. The K-depleted biotite changed from greenish-black through yellow to pale gray whereas the natural biotite changed from greenish-black through beige to yellow. However, in the case of K-depleted phlogopite, there was no significant color change during the transformation process. The presence of the interlayer K+ ions and the structural Fe2+ ions in mica appear to have contributed to the differences in the degree of weathering to kaolinite among the micas investigated.

Keywords

Hydrothermal TreatmentHydroxy Al-interlayered Vermiculite (HIV)KaoliniteK-depleted BiotiteK-depleted PhlogopiteTransformationWeathering
Type
Research Article
Information
Clays and Clay Minerals , Volume 55 , Issue 6 , December 2007 , pp. 565 - 571
Copyright
Copyright © 2007, The Clay Minerals Society

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