Self-Assembly of Cetyltrimethylammonium Bromide and Lamellar Zeolite Precursor for the Preparation of Hierarchical MWW Zeolite

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• 作者：Le Xu ; Xinyi Ji ; Shenhui Li ; Zhengyang Zhou ; Xin Du ; Junliang Sun ; Feng Deng ; Shunai Che ; Peng Wu
• 刊名：Chemistry of Materials
• 出版年：2016
• 出版时间：June 28, 2016
• 年：2016
• 卷：28
• 期：12
• 页码：4512-4521
• 全文大小：665K
• 年卷期：0
• ISSN：1520-5002

文摘

Construction of hierarchical zeolite catalysts from lamellar zeolite precursor is challenging and promising for industrial catalysis. Although numerous efforts have been dedicated to control the organization of zeolite nanosheets by postsynthetic approaches or employing complex surfactants in hydrothermal synthesis, there is still no successful case that the hierarchical lamellar zeolite is hydrothermally synthesized by the self-assembly of the commercially available simple surfactant cetyltrimethylammonium bromide (CTAB) and inorganic zeolite precursor. In traditional syntheses, the self-assembly of simple surfactants and the growth of microporous framework are hardly compatible from both thermodynamic and kinetic viewpoints, preferring to cause phase separation. Herein, we approach for the first time the hydrothermal synthesis of a mesostructured multilamellar zeolite ECNU-7P, consisting of an alternative stacking of inorganic MWW zeolite nanosheets and organic CTAB layers with large interlayer spacing (25 Å), by a zeolite seed and CTAB-assisted dissolution–recrystallization route. Correlated 2D ¹H–²⁹Si solid-state NMR, X-ray, electron microscopy, and rotation electron diffraction analyses provide molecular-level insights into the guest–host interactions between organic surfactant and inorganic framework during the self-assembly and structure evolution process. Moreover, the calcined Al-ECNU-7 possessing a hierarchical mesostructure proves to serve as a highly active, selective, and stable solid acid catalyst for triisopropylbenzene cracking as well as acylation of anisole.