Li Wen-Cui, Lu An-Hui, Palkovits Regina, Schmidt Wolfgang, Spliethoff Bernd, Schüth Ferdi
Contribution from the Max-Planck-Institut für Kohlenforschung, Kaiser-Wilhelm-Platz 1, D-45470 Mülheim an der Ruhr, Germany.
J Am Chem Soc. 2005 Sep 14;127(36):12595-600. doi: 10.1021/ja052693v.
In this study, we present a synthetic pathway for the fabrication of self-supporting zeolite monoliths consisting of crystallized nanoparticles. A resorcinol-formaldehyde-based organic aerogel is used as a template, and silicalite-1 is used as the zeolite example. The silicalite-1 monoliths obtained consist of individual well-defined zeolite nanocrystals with sizes of 30-40 nm. The monoliths exhibit a high mechanical stability and have hierarchical porosity, with micropores within the zeolite particles, a mesopore system formed by the packing of the nanoparticles, and a macropore system on the monolith level. Such monolithic zeolites show high selectivity typically above 80% to epsilon-caprolactam combined with a high rate of reaction of 0.46 g(caprolactame)/(g(catalyst).h) in the Beckmann rearrangement of cyclohexanone oxime.
在本研究中,我们展示了一种用于制备由结晶纳米颗粒组成的自支撑沸石整体材料的合成途径。以间苯二酚 - 甲醛为基础的有机气凝胶用作模板,硅沸石 -1用作沸石示例。所获得的硅沸石 -1整体材料由尺寸为30 - 40纳米的单个明确的沸石纳米晶体组成。这些整体材料表现出高机械稳定性并具有分级孔隙率,在沸石颗粒内有微孔,由纳米颗粒堆积形成的介孔系统,以及在整体材料层面上的大孔系统。这种整体沸石在环己酮肟的贝克曼重排反应中,对ε-己内酰胺表现出通常高于80%的高选择性,同时反应速率高达0.46克(己内酰胺)/(克(催化剂)·小时)。