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Some observations on the preparation and properties of colloidal silicalites. Part I: synthesis of colloidal silicalite-1 and titanosilicalite-1 (TS-1)

奥斯特瓦尔德成熟 结晶 胶体 晶体生长 胶体晶体 胶体二氧化硅 Crystal(编程语言) 沸石 化学工程 材料科学 化学 结晶学 纳米技术 催化作用 物理化学 有机化学 程序设计语言 工程类 计算机科学 涂层
作者
Colin S. Cundy,James O. Forrest,R.J. Plaisted
出处
期刊:Microporous and Mesoporous Materials [Elsevier BV]
卷期号:66 (2-3): 143-156 被引量:104
标识
DOI:10.1016/j.micromeso.2003.08.021
摘要

Possible methods for the preparation of colloidal zeolite sols are discussed: direct synthesis is at present the only practicable procedure. The linear crystal growth rate for colloidal TS-1 (≈2.5 at.% Ti) at 175 °C was estimated to be ⩽80 nm h−1, which is lower than that for colloidal silicalite by at least a factor of 3. The introduction of titanium also caused a reduction in the number of crystals nucleated. These effects are ascribed to the difficulty of incorporating the heteroelement into the lattice. No evidence for Ostwald ripening in colloidal silicalite synthesis was found, even at long reaction times. In seeded growth experiments at 100 °C, (i) TPA-silicalite-1 product crystal size could be closely controlled by the quantity of 43 nm seed added, and (ii) crystal linear growth rates in thermally and microwave heated reactions were the same within experimental error. Ageing the precursor sols at 22 °C before crystallisation at 90–175 °C (microwave or thermal heating) demonstrated the generation of proto-nuclei during the room-temperature ageing process. On subsequent heating, these mature into viable nuclei and grow into crystals. An interpretation of this behaviour establishes the relationship of the present results to those of other workers. This identifies the generation of nuclei with a series of chemical steps which lead from the initial equilibration reactions to the formation of the primary replicating unit.

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