化学
煅烧
硅酸盐
结晶
碱金属
氟化物
离子键合
固态
退火(玻璃)
离子
固溶体
无机化学
沸石
金属
矿物学
催化作用
物理化学
有机化学
冶金
材料科学
作者
J.M. Chézeau,L. Delmotte,J.L. Guth,Z. Gabélica
出处
期刊:Zeolites
[Elsevier]
日期:1991-07-01
卷期号:11 (6): 598-606
被引量:116
标识
DOI:10.1016/s0144-2449(05)80011-9
摘要
The formation and annealing of various kinds of defects in the framework of highly siliceous MFI-type zeolites, as evidenced by high-resolution solid-state 29Si n.m.r., can be explained by considering the systematic influence of synthesis parameters and postsynthesis treatments. High pH values and high concentrations of alkali metal and fluoride ions prevent a complete polycondensation of the silicate species and generate materials that contain significant levels of nonbonding point defects. By contrast, a high crystallization temperature results in the ready hydrolysis of the terminal Si-O− groups, leading to structures containing fewer defects. A large number of T vacancies (hydroxyl nests) are created in zeolites crystallized at low temperatures in the presence of high Pr4N+ concentations and in the absence of F− or Na+ ions. Such conditions favor the formation of double-5-ring silicate anions. The hypothesis, that such species may further condense, conducting to frameworks with an important number of empty T-sites, is proposed. On the basis of these findings, ideal synthesis conditions can be proposed to produce (Si) MFI zeolites that contain a minimum number of defects. Various postsynthesis treatments, namely, different calcination conditions followed, or preceded, by selected ionic (akali cation) exchanges, result in a partial or a nearly total healing of these defects in the final materials.
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