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引导沸石结构形成分级纳米多孔结构。

Directing zeolite structures into hierarchically nanoporous architectures.

机构信息

Center for Functional Nanomaterials, Department of Chemistry, KAIST, Daejeon 305-701, Korea.

出版信息

Science. 2011 Jul 15;333(6040):328-32. doi: 10.1126/science.1204452.

Abstract

Crystalline mesoporous molecular sieves have long been sought as solid acid catalysts for organic reactions involving large molecules. We synthesized a series of mesoporous molecular sieves that possess crystalline microporous walls with zeolitelike frameworks, extending the application of zeolites to the mesoporous range of 2 to 50 nanometers. Hexagonally ordered or disordered mesopores are generated by surfactant aggregates, whereas multiple cationic moieties in the surfactant head groups direct the crystallization of microporous aluminosilicate frameworks. The wall thicknesses, framework topologies, and mesopore sizes can be controlled with different surfactants. The molecular sieves are highly active as catalysts for various acid-catalyzed reactions of bulky molecular substrates, compared with conventional zeolites and ordered mesoporous amorphous materials.

摘要

结晶介孔分子筛一直被视为用于涉及大分子的有机反应的固体酸催化剂。我们合成了一系列具有沸石骨架的结晶微孔壁的介孔分子筛,将沸石的应用扩展到 2 至 50 纳米的介孔范围。六方有序或无序的介孔是通过表面活性剂聚集体产生的,而表面活性剂头基中的多个阳离子部分则指导微孔铝硅酸盐骨架的结晶。不同的表面活性剂可以控制壁厚度、骨架拓扑结构和介孔尺寸。与传统沸石和有序介孔无定形材料相比,这些分子筛作为大体积分子底物的各种酸催化反应的催化剂具有很高的活性。

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