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Effects of a Protic Ionic Liquid on the Reaction Pathway during Non-Aqueous Sol–Gel Synthesis of Silica: A Raman Spectroscopic Investigation

机译:质子离子液体对二氧化硅非水溶胶-凝胶合成过程中反应路径的影响:拉曼光谱研究

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摘要

The reaction pathway during the formation of silica via a two-component “non-aqueou” sol-gel synthesis is studied by in situ time-resolved Raman spectroscopy. This synthetic route is followed with and without the addition of the protic ionic liquid 1-ethylimidazolium bis(trifluoromethanesulfonyl)imide (C2HImTFSI) in order to investigate its effect on the reaction pathway. We demonstrate that Raman spectroscopy is suitable to discriminate between different silica intermediates, which are produced and consumed at different rates with respect to the point of gelation. We find that half-way to gelation monomers and shorter chains are the most abundant silica species, while the formation of silica rings strongly correlates to the sol-to-gel transition. Thus, curling up of linear chains is here proposed as a plausible mechanism for the formation of small rings. These in turn act as nucleation sites for the condensation of larger rings and thus the formation of the open and polymeric silica network. We find that the protic ionic liquid does not change the reaction pathway per se, but accelerates the cyclization process, intermediated by the faster inclusion of monomeric species.
机译:通过原位时间分辨拉曼光谱研究了通过两组分“非水”溶胶-凝胶合成形成二氧化硅的反应途径。为了研究其对反应途径的影响,在有或没有添加质子离子液体1-乙基咪唑双(三氟甲磺酰基)酰亚胺(C2HImTFSI)的情况下遵循该合成途径。我们证明拉曼光谱法适于区分不同的二氧化硅中间体,这些中间体相对于胶凝点以不同的速率产生和消耗。我们发现,到凝胶化过程中途的单体和较短的链是最丰富的二氧化硅种类,而二氧化硅环的形成与溶胶-凝胶转变密切相关。因此,这里提出线性链的卷曲是形成小环的合理机制。这些继而充当较大环的缩合的成核位点,从而形成开放的聚合二氧化硅网络。我们发现,质子离子液体本身并不会改变反应路径,但会加快环化过程,并以更快地包含单体种类为中介。

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