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Organomineral Derivatives Obtained by Reacting Organochlorosilanes with the Surface of Silicates in Organic Solvents

Published online by Cambridge University Press:  01 July 2024

E. Ruiz-Hitzky  and
J. J. Fripiat
E. Ruiz-Hitzky*
Affiliation:
University of Louvain, Laboratoire de Physico-Chimie Minérale, Place Croix du Sud 1, 1348, Louvain-la-Neuve, Belgium
J. J. Fripiat*
Affiliation:
University of Louvain, Laboratoire de Physico-Chimie Minérale, Place Croix du Sud 1, 1348, Louvain-la-Neuve, Belgium
*
*Instituto de Edafología y Biología Vegetal, C.S.I.C., c/Serrano 115 dpdo., Madrid 6.
†Centre de Recherche sur les Solides á Organisation Cristalline Imparfaite, C.N.R.S., Orleans-Cedex, 45045, France.
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Abstract

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Stable organomineral derivatives are formed by reaction of organochlorosilanes with certain phyllosilicates. Organosiloxyl functions are grafted on silanol groups present at external mineral surfaces.

Water molecules adsorbed on external mineral surfaces may cause hydrolysis of the reactant organosilicon products, with liberation of HCl. This, in turn, may react with the silicate: octahedral cations are extracted from the lattice and fresh Si-OH groups, capable of further grafting, are formed on the mineral surface.

On the other hand, when difunctional reagents such as methylvinyldichlorosilane are used and if the ratio of adsorbed water to added reactive is adequate, then polymeric species with polysiloxane chains are grafted on the mineral.

Because of its high content of silanol groups, sepiolite forms organomineral compounds having a relatively high organic matter content. With chrysotile, the amount of organic matter grafted to the silicate, is considerably smaller, but it increases appreciably if water is added to the reacting products. This is attributed to hydrolysis of the organic reactant and subsequent destruction of external “brucitic” layers by acid attack.

Type
Research Article
Information
Clays and Clay Minerals , Volume 24 , Issue 1 , February 1976 , pp. 25 - 30
Copyright
Copyright © 1976 The Clay Minerals Society

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