Recent advances in the synthesis of hierarchically nanoporous zeolites

Recent advances in the development of synthesis strategies for hierarchically nanoporous zeolites are comprehensively reviewed. [Display omitted] ► Recent advances in the synthesis of hierarchically nanoporous zeolite are reviewed. ► Post-synthetic demetallation for the generation of mesoporosity. ►...

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Published inMicroporous and mesoporous materials Vol. 166; pp. 3 - 19
Main Authors Na, Kyungsu, Choi, Minkee, Ryoo, Ryong
Format Journal Article Conference Proceeding
LanguageEnglish
Published San Diego, CA Elsevier Inc 15.01.2013
Elsevier
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Summary:Recent advances in the development of synthesis strategies for hierarchically nanoporous zeolites are comprehensively reviewed. [Display omitted] ► Recent advances in the synthesis of hierarchically nanoporous zeolite are reviewed. ► Post-synthetic demetallation for the generation of mesoporosity. ► Hard- and soft-templating synthesis strategy. ► Zeolite-structure-directing surfactant-driven synthesis route. ► Catalytic contributions of hierarchically nanoporous zeolites. Hierarchically nanoporous zeolites possessing mesopores as well as the inherent micropores of zeolite structures are garnering attention as a solution to the diffusion limitation problem of solely microporous classical zeolites. The hierarchical structure enables zeolites to have maximum structural functions in a limited space and volume owing to the high diffusion efficiency. Hierarchical zeolites are in high demand for the development of advanced materials for applications in adsorption, separation and catalysis. Herein, recent advances in synthesis routes to hierarchically nanoporous zeolites are reviewed with their catalytic contributions. Particular emphasis is given to the recently developed synthesis method which uses surfactants that are functionalized with a zeolite-structure-directing group. This type of surfactants can direct porous structures in micro- and meso-length scales simultaneously.
ISSN:1387-1811
1873-3093
DOI:10.1016/j.micromeso.2012.03.054