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Clays and Clay Minerals; June 2002; v. 50; no. 3; p. 306-313
© 2002 Clay Minerals Society
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INFRARED EVIDENCE OF DIOCTAHEDRAL-TRIOCTAHEDRAL SITE OCCUPANCY IN PALYGORSKITE

A. Chahi1, S. Petit2,* and A. Decarreau2

1 Université Cadi Ayyad, Faculté des Sciences Semlalia, Boulevard Prince Moulay Abdellah, BP S.15 Marrakech, Morocco
2 Université de Poitiers, UMR 6532 CNRS ’HydrASA’, 40, Avenue du Recteur Pineau, F-86022 Poitiers Cedex, France

* E-mail address of corresponding author: sabine.petit{at}hydrasa.univ-poitiers.fr

A Mg-rich palygorskite sample from phosphorite deposits of Ganntour (Morocco) with the structural formula Si8(Mg2.6Al1.19Fe0.33III{square}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{square}OH, AlFe{square}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.

Key Words: Cation Distribution • FTIR Spectroscopy • Octahedral Occupancy • Palygorskite




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