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      Onset of Propene Oligomerization Reactivity in ZSM-5 Studied by Inelastic Neutron Scattering Spectroscopy

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          Abstract

          The techniques of quasi-elastic and inelastic neutron scattering (QENS and INS) are applied to investigate the oligomerization of propene over a ZSM-5 zeolite. Investigations are performed at low temperatures, allowing identification of the onset of the oligomerization reaction and observation of the low-energy spectral changes due to intermediate formation that are difficult to observe by optical methods. Oligomerization proceeds via formation of a hydrogen-bonded precursor by an interaction of the propene with an internal acid site followed by protonation and chain growth with protonation being the rate-limiting step. The use of quasi-elastic neutron scattering to observe changes in system mobility with temperature via the elastic window scan technique allows identification of the active temperature range where catalyst activity commences and permits targeting of the more time-consuming INS investigations to conditions of interest. From examination of the product’s spectrum, the structure of the resulting oligomer is deduced to be primarily linear.

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          Most cited references30

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          Mantid—Data analysis and visualization package for neutron scattering and\(\mathrm{\mu }\)SR experiments

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            Recent trends and fundamental insights in the methanol-to-hydrocarbons process

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              The formation and degradation of active species during methanol conversion over protonated zeotype catalysts.

              The methanol to hydrocarbon (MTH) process provides an efficient route for the conversion of carbon-based feedstocks into olefins, aromatics and gasoline. Still, there is room for improvements in product selectivity and catalytic stability. This task calls for a fundamental understanding of the formation, catalytic mechanism and degradation of active sites. The autocatalytic feature of the MTH process implies that hydrocarbons are active species on the one hand and deactivating species on the other hand. The steady-state performance of such species has been thoroughly studied and reviewed. However, the mechanism of formation of the initial hydrocarbon species (i.e.; the first C-C bond) and the evolution of active species into deactivating coke species have received less attention. Therefore, this review focuses on the significant progress recently achieved in these two stages by a combination of theoretical calculations, model studies, operando spectroscopy and catalytic tests.
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                Author and article information

                Journal
                ACS Omega
                ACS Omega
                ao
                acsodf
                ACS Omega
                American Chemical Society
                2470-1343
                30 March 2020
                14 April 2020
                : 5
                : 14
                : 7762-7770
                Affiliations
                []School of Chemistry, University of Glasgow , Joseph Black Building, Glasgow G12 8QQ, U.K.
                []UK Catalysis Hub, Research Complex at Harwell, STFC Rutherford Appleton Laboratory , Chilton, Oxon OX11 0FA, U.K.
                [§ ]ISIS Neutron and Muon Source, STFC Rutherford Appleton Laboratory , Chilton, Oxon OX11 0QX, U.K.
                []Johnson Matthey Technology Centre , Blounts Court, Sonning Common, Reading RG4 9NH, U.K.
                []Department of Chemistry, University of Aberdeen , Aberdeen AB24 3UE, U.K.
                Author notes
                Article
                10.1021/acsomega.9b03503
                7160849
                4325ead6-0142-4700-81e4-cf83891d9da9
                Copyright © 2020 American Chemical Society

                This is an open access article published under a Creative Commons Attribution (CC-BY) License, which permits unrestricted use, distribution and reproduction in any medium, provided the author and source are cited.

                History
                : 20 October 2019
                : 20 February 2020
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                ao9b03503

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