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ZSM-5沸石上乙醇制烯烃反应中三配位铝物种的研究

Insight into Three-Coordinate Aluminum Species on Ethanol-to-Olefin Conversion over ZSM-5 Zeolites.

作者信息

Wang Zichun, O'Dell Luke A, Zeng Xin, Liu Can, Zhao Shufang, Zhang Wenwen, Gaborieau Marianne, Jiang Yijiao, Huang Jun

机构信息

Laboratory for Catalysis Engineering, School of Chemical and Biomolecular Engineering & Sydney Nano Institute, The University of Sydney, Sydney, NSW, 2006, Australia.

Department of Engineering, Macquarie University, Sydney, NSW, 2109, Australia.

出版信息

Angew Chem Int Ed Engl. 2019 Dec 9;58(50):18061-18068. doi: 10.1002/anie.201910987. Epub 2019 Oct 30.

Abstract

Commercial bioethanol can be readily converted into ethylene by a dehydration process using solid acids, such as Brønsted acidic H-ZSM-5 zeolites, and thus, it is an ideal candidate to replace petroleum and coal for the sustainable production of ethylene. Now, strong Lewis acidic extra-framework three-coordinate Al species were introduced into H-ZSM-5 zeolites to improve their catalytic activity. Remarkably, Al species working with Brønsted acid sites can accelerate ethanol dehydration at a much lower reaction temperature and shorten the unsteady-state period within 1-2 h, compared to >9 h for those without Al species, which can significantly enhance the ethanol dehydration efficiency and reduce the cost. The reaction mechanism, studied by solid-state NMR, shows that strong Lewis acidic EFAl-Al species can collaborate with Brønsted acid sites and promote ethanol dehydration either directly or indirectly via an aromatics-based cycle to produce ethylene.

摘要

商业生物乙醇可通过使用固体酸(如布朗斯台德酸性H-ZSM-5沸石)的脱水过程轻松转化为乙烯,因此,它是替代石油和煤炭以可持续生产乙烯的理想候选物。现在,将强路易斯酸性的骨架外三配位铝物种引入H-ZSM-5沸石中以提高其催化活性。值得注意的是,与不含铝物种的情况相比,与布朗斯台德酸位点协同作用的铝物种可在低得多的反应温度下加速乙醇脱水,并将非稳态期缩短至1-2小时以内,而不含铝物种的情况则>9小时,这可显著提高乙醇脱水效率并降低成本。通过固体核磁共振研究的反应机理表明,强路易斯酸性的骨架外铝物种(EFAl-Al)可与布朗斯台德酸位点协同作用,并通过基于芳烃的循环直接或间接促进乙醇脱水以生成乙烯。

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