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Sol-gel preparation of mesoporous Al2O3-SiO2 glasses: structural evolution monitored by solid state NMR

机译:溶胶-凝胶法制备介孔Al2O3-SiO2玻璃:通过固态NMR监测结构演变

摘要

Glasses along the composition line 0.5Al2O3–xSiO2 (1 ≤ x ≤ 6) were prepared via a novel sol-gel route using tetraethylorthosilicate and aluminum lactate as precursors. The structural evolution from solution to gel to glass is monitored by standard 27Al and 29Si nuclear magnetic resonance (NMR) spectroscopies, revealing important insights about molecular level mechanisms occurring at the various stages of glass formation. Under the experimental conditions reported, silica and alumina precursors undergo homoatomic condensation processes when the gel is heat treated at about 100 and 300 °C, respectively, and only little heteroatomic co-condensation occurs in this temperature range. The latter is promoted only upon elimination of the residual lactate and water ligands upon annealing the gels above 300 °C. Following calcination at 650 °C, mesoporous glasses are obtained, having average pore diameter of about 3 nm and a surface areas near 500 m2/g. Si-O-Al connectivities are detected by 29Si magic angle spinning (MAS)-NMR. 27Al MAS-NMR spectra reveal aluminum in four-, five- and six-coordination. The spectra differ significantly from those of other sol-gel derived Al2O3-SiO2 materials prepared from different precursor routes, suggesting that the lactate route results in a higher degree of compositional homogeneity.
机译:沿组成线0.5Al2O3-xSiO2(1≤x≤6)的玻璃是通过新颖的溶胶凝胶法制备的,使用原硅酸四乙酯和乳酸铝作为前体。通过标准的27Al和29Si核磁共振(NMR)光谱监测从溶液到凝胶再到玻璃的结构演变,揭示了有关在玻璃形成各个阶段发生的分子水平机制的重要见解。在报道的实验条件下,当凝胶分别在约100和300°C进行热处理时,二氧化硅和氧化铝前体会经历均相缩合过程,在此温度范围内只有很少的杂原子共缩合发生。只有在300°C以上的凝胶退火后,消除残留的乳酸和水配体后,才能促进后者。在650℃下煅烧后,获得具有约3nm的平均孔径和约500m2 / g的表面积的中孔玻璃。 Si-O-Al连接性通过29Si幻角旋转(MAS)-NMR检测。 27Al MAS-NMR光谱显示铝的四,五和六配位。光谱与由不同前体路线制得的其他溶胶-凝胶衍生的Al2O3-SiO2材料的光谱存在显着差异,这表明乳酸路线导致了更高的组成均匀性。

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