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Infrared Evidence of Dioctahedral-Trioctahedral Site Occupancy in Palygorskite

Published online by Cambridge University Press:  01 January 2024

A. Chahi
Affiliation:
Université Cadi Ayyad, Faculté des Sciences Semlalia, Boulevard Prince Moulay Abdellah, BP S.15 Marrakech, Morocco
S. Petit*
Affiliation:
Universite de Poitiers, UMR 6532 CNRS ‘HydrASA’, 40, Avenue du Recteur Pineau, F-86022 Poitiers Cedex, France
A. Decarreau
Affiliation:
Universite de Poitiers, UMR 6532 CNRS ‘HydrASA’, 40, Avenue du Recteur Pineau, F-86022 Poitiers Cedex, France
*
*E-mail address of corresponding author: sabine.petit@hydrasa.univ-poitiers.fr
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Abstract

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A Mg-rich palygorskite sample from phosphorite deposits of Ganntour (Morocco) with the structural formula Si8(Mg2.6Al1.19Fe0.33III□0.88)Ca0.056Na0.024K0.104O20(OH)2(OH2)4⋅4H2O, was studied by FTIR spectroscopy. In both OH-stretching and OH-bending regions, there is evidence of dioctahedral Al2□OH, AlFe□OH and trioctahedral Mg3OH features, leading to a di-trioctahedral crystallochemical model of octahedral site occupancies in ribbons of Ganntour palygorskite.

This model, established through the IR spectroscopy study of a Mg-rich palygorskite, seems to be appropriate for many other palygorskites with lower Mg content in the octahedral sheet.

Type
Research Article
Copyright
Copyright © 2002, The Clay Minerals Society

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