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Study of the hydrolysis and condensation of γ-Aminopropyltriethoxysilane by FT-IR spectroscopy

机译:FT-IR光谱研究γ-氨丙基三乙氧基硅烷的水解缩合反应

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摘要

The hydrolysis and condensation reactions of γ-APS have been studied in different acid content aqueous solution by using Fourier Transform infrared (FT-IR) spectroscopy. The hydrolysis of γ-APS under the studied conditions can be followed by the increase of the ethanol band located at 882 cm?1 and the decrease of the band due to the ρ(CH3) of γ-APS molecules located at 959 cm?1. Hydrolysis reaction is faster by increasing both H2O and acid concentrations, and it is completed when 3 moles of H2O per mole of γ-APS are used. The increase of the vibrational band located at 1146 cm?1 shows that condensation of the hydrolysed γ-APS molecules take place forming linear chains in poorly cross-linked structures. Besides, both 8-membered cyclic siloxane formations and poorly cross-linked structures are formed and increase as the water and acid content are increased. On the other hand, highly connected cross-linked structures do not appear due to the steric hindrance of the non-hydrolysable aminopropyl group. The silanol band shows that hydrolysis is faster than condensation except for samples with the lowest H2O content.
机译:通过傅立叶变换红外光谱(FT-IR)研究了在不同酸含量的水溶液中γ-APS的水解和缩合反应。在所研究的条件下,γ-APS的水解可以通过增加位于882 cm?1 处的乙醇带和由于γ-的ρ(CH3 )引起的带的减小来实现。 APS分子位于959 cm?1 。通过同时增加H2O和酸浓度,水解反应更快,并且每摩尔γ-APS使用3摩尔H2O即可完成水解反应。 1146 cm?1处振动带的增加表明水解的γ-APS分子发生缩合,形成交联不良的线性链。此外,随着水和酸含量的增加,形成了8元环状硅氧烷并形成了不良的交联结构。另一方面,由于不可水解的氨丙基的位阻,没有出现高度连接的交联结构。硅烷醇谱带表明,除具有最低H2O含量的样品外,水解比缩合反应快。

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