Preparation of sol-gel hybrid materials from gamma-methacryloxypropyltrimethoxysilane and tetramethyl orthosilicate: study of the hydrolysis and condensation reactions
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Preparation of sol-gel hybrid materials from gamma-methacryloxypropyltrimethoxysilane and tetramethyl orthosilicate: study of the hydrolysis and condensation reactions
Citation:
Colloid and Polymer Science, (2011), 289(17-18), 1875-1883.
ISSN:
0303-402X (Print) 1435-1536 (Online)
DOI:
10.1007/s00396-011-2504-y
Sponsor:
This work has been supported by the Ministry of Science and Innovation of Spain (Projects MAT2006-04486 and MAT2009-13530) and the Regional Community of Madrid (Project 2009/MAT-1585). AA El hadad acknowledges a predoctoral contract JAE financed by CSIC, and VB acknowledges a Ramon y Cajal researcher contract financed by CSIC-MICINN
Organic-inorganic hybrid materials suitable for the development of sol&-gel coatings for metallic surfaces were prepared by hydrolysis and condensation of gamma-methacryloxypropyltrimethoxysilane (MAPTMS) and tetramethyl orthosilicate (TMOS). The hydrolysis ofOrganic-inorganic hybrid materials suitable for the development of sol&-gel coatings for metallic surfaces were prepared by hydrolysis and condensation of gamma-methacryloxypropyltrimethoxysilane (MAPTMS) and tetramethyl orthosilicate (TMOS). The hydrolysis of MAPTMS/TMOS was carried out in an ethanol/water solution. The prehydrolysis stage of MAPTMS/TMOS system was monitored by Fourier transform infrared spectroscopy (FTIR) and liquid-state 29Si and 13C nuclear magnetic resonance (29Si and 13C NMR). FTIR analysis indicated that the hydrolysis of MAPTMS/TMOS was accomplished as far as the (SiOMe) band corresponding to unhydrolyzed silane disappeared. The concentration of the alkoxy groups and the extent of self-condensation of mono-, di-, and trisubstituted siloxanes (T species) in the sol were estimated by using liquid-state 29Si NMR spectroscopy. The hydrolysis of the prepared sol was also evaluated by liquid-state 13C NMR spectroscopy. The results indicated that under the adopted synthesis strategy conditions, the hydrolysis process requires 4 h to be completed.[+][-]