Issue 8, 2005

Silylation of laponite clay particles with monofunctional and trifunctional vinyl alkoxysilanes

Abstract

We report in this work the grafting of laponite clay particles with monofunctional γ-methacryloxypropyl dimethyl methoxy silane (γ-MPTDES) and trifunctional γ-methacryloxypropyl trimethoxy silane (γ-MPTMS) coupling agents. The evolution of the grafted amount and of the grafting yield was monitored as a function of the reaction time and of the initial silane concentration. We showed that the grafted amount increased with time and with the silane content up to a plateau value. The amount of chemisorbed silane at saturation varied from 0.56 to 1.9 mmol g−1 depending on the nature of the coupling agent, the reaction time and the grafting conditions. While the trifunctional silane was capable of both reaction with the clay edges and formation of complex polysiloxane oligomers in the bulk which were further deposited on the particulate surface, the monofunctional silane formed a monolayer coverage on the border of the clay plates with the carbonyl groups being directed toward the surface as attested by Fourier transform infrared (FTIR) spectroscopy. The properties of the organosilane-modified laponite were examined by various analytical techniques such as wide-angle X-ray diffraction (WAXD), nitrogen adsorption and thermogravimetric analysis (TGA). The monofunctional silane exhibited nearly no effect on the physicochemical properties of the clay whereas grafting of the trifunctional silane resulted in decreased porosity, increased interlamellar distance and higher hydrophobicity.

Graphical abstract: Silylation of laponite clay particles with monofunctional and trifunctional vinyl alkoxysilanes

Supplementary files

Article information

Article type
Paper
Submitted
08 Oct 2004
Accepted
17 Nov 2004
First published
13 Dec 2004

J. Mater. Chem., 2005,15, 863-871

Silylation of laponite clay particles with monofunctional and trifunctional vinyl alkoxysilanes

N. N. Herrera, J. Letoffe, J. Reymond and E. Bourgeat-Lami, J. Mater. Chem., 2005, 15, 863 DOI: 10.1039/B415618H

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