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Modeling the Adsorption of Organic Dye Molecules to Kaolinite

Published online by Cambridge University Press:  01 January 2024

Rodney G. Harris*
Affiliation:
Colloid and Environmental Chemistry Laboratory, La Trobe University, PO Box 199, Bendigo, Victoria 3552, Australia
John D. Wells*
Affiliation:
Colloid and Environmental Chemistry Laboratory, La Trobe University, PO Box 199, Bendigo, Victoria 3552, Australia
Michael J. Angove
Affiliation:
Colloid and Environmental Chemistry Laboratory, La Trobe University, PO Box 199, Bendigo, Victoria 3552, Australia
Bruce B. Johnson
Affiliation:
Colloid and Environmental Chemistry Laboratory, La Trobe University, PO Box 199, Bendigo, Victoria 3552, Australia
*
Present address: Brewing Research International, Lyttel Hall, Nutfield, Surrey RH1 4HY, UK
*E-mail address of corresponding author: j.wells@latrobe.edu.au
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Abstract

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Simple extended constant capacitance surface complexation models have been developed to represent the adsorption of polyaromatic dyes (9-aminoacridine, 3,6-diaminoacridine, azure A and safranin O) to kaolinite, and the competitive adsorption of the dyes with Cd. The formulation of the models was based on data from recent publications, including quantitative adsorption measurements over a range of conditions (varying pH and concentration), acid-base titrations and attenuated total reflectance-Fourier transform infrared spectroscopic data. In the models the dye molecules adsorb as aggregates of three or four, forming outer-sphere complexes with sites on the silica face of kaolinite. Both electrostatic and hydrophobic interactions are implicated in the adsorption processes. Despite their simplicity, the models fit a wide range of experimental data, thereby supporting the underlying hypothesis that the flat, hydrophobic, but slightly charged silica faces of kaolinite facilitate the aggregation and adsorption of the flat, aromatic, cationic dye molecules.

Type
Research Article
Copyright
Copyright © 2006, The Clay Minerals Society

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