Claudine Dorémieux-Morin *, Claudine Martin, Jean-Marie Brégeault, Jacques Fraissard
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引用次数: 32
摘要
商用硅铝含有与氧四和六配位的铝原子。在370 K以上的温度下,在1 Pa条件下脱水后,其1h MAS NMR谱显示硅醇基团和OH与铝原子成键,但没有酸性桥接OH基团。在较低温度下脱水的样品光谱为这种酸性OH基团提供了明确的证据。低硅浓度二氧化硅-氧化铝的29Si MAS和CP-MAS NMR谱主要表现为SiO4四面体和硅原子与OH基团的键合,其29Si的化学位移比通常归因于端SiOH或双相Si(OH)2的化学位移要高。共沉淀法制备的SiO2:Al2O3 = 75:25样品中SiO4四面体的环境是随机的。
Multinuclear high-resolution solid-state nuclear magnetic resonance studies of amorphous silica-aluminas
Commercial silica-aluminas contain aluminium atoms tetra- and hexacoordinated to oxygen. After dehydration at 1 Pa at temperatures above 370 K, their1H MAS NMR spectra show silanol groups and OH groups bonded to aluminium atoms but no acidic bridging OH groups. Spectra of samples dehydrated at lower temperature give clear evidence for such acidic OH groups.29Si MAS and CP-MAS NMR spectra of silica-aluminas with low silica concentration show mainly SiO4 tetrahedra bonded to four others and silicon atoms, bonded to OH groups, whose29Si chemical shift is upfield of that generally attributed to terminal SiOH or geminal Si(OH)2. The environment of SiO4 tetrahedra in the sample with SiO2:Al2O3 = 75:25, prepared by coprecipitation, is random.