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Crystal Growth of Layered Silicate Grafted with Organic Groups on Monodisperse Spherical Silica Particles

Published online by Cambridge University Press:  01 January 2024

Masahiro Yamauchi
Affiliation:
Department of Chemistry and Materials Engineering, Shinshu University, Nagano 380-8553, Japan
Tomohiko Okada*
Affiliation:
Department of Chemistry and Materials Engineering, Shinshu University, Nagano 380-8553, Japan
*
*E-mail address of corresponding author: [email protected]
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Abstract

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Control of the structure and morphology of clay crystals presents a challenge in the synthesis of materials for adsorption and catalysis. In the present study, direct crystallization of a phyllosilicate grafted with organosilyl (methylsilyl and phenylsilyl) groups on the surface of monodisperse spherical silica particles (2.6 μm) is reported. Methyl- and phenyltriethoxysilanes were allowed to react hydrothermally in a Teflon-lined autoclave with silica, MgCl2, and LiF in the presence of urea for 2 or 4 days. X-ray diffraction patterns revealed that the fine platy particles formed were a trioctahedral hectorite-like layered silicate. Greater temperature (150°C) was required to achieve homogeneous coverage of the original spherical silica particles with the hectorite-like particles. The diameter of the initial silica grains increased slightly to 3.0 μm after the hydrothermal reactions, while the original spherical shape and size distribution were maintained. Solid-state 29Si nuclear magnetic resonance analyses confirmed that the presence of resonances attributed to the RSi(OMg)(OSi)2 and RSi(OMg)(OH)(OSi) (R = methyl or phenyl) environments of the silicon proved the formation of covalent bonds between phyllosilicate sheets and the organic moieties. The crystallinity of the layered silicates increased when the reactions ran for a longer time (4 days).

Type
Article
Copyright
Copyright © Clay Minerals Society 2018

Footnotes

This paper was originally presented during the session ‘NT-11. Material's Challenges for Clay Scientist’ during ICC 2017

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