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dc.date.accessioned2020-02-11T19:26:15Z
dc.date.available2020-02-11T19:26:15Z
dc.date.created2018-07-16T09:47:33Z
dc.date.issued2018
dc.identifier.citationPinilla-Herrero, Irene Borfecchia, Elisa Holzinger, Julian Mentzel, Uffe V. Joensen, Finn Lomachenko, Kirill A. Bordiga, Silvia Lamberti, Carlo Berlier, Gloria Olsbye, Unni Svelle, Stian Skibsted, Jørgen Beato, Pablo . High Zn/Al ratios enhance dehydrogenation vs hydrogen transfer reactions of Zn-ZSM-5 catalytic systems in methanol conversion to aromatics. Journal of Catalysis. 2018, 362, 146-163
dc.identifier.urihttp://hdl.handle.net/10852/72985
dc.description.abstractTwo series of Zn-ZSM-5 catalysts were prepared by ion exchanging two commercial zeolites with different Si/Al ratios (40 and 15) with increasing Zn loadings. The nature of the Zn sites in the zeolite was studied by spectroscopy using laboratory and synchrotron techniques. All the evidences suggest that catalytic activity is associated with [Zn(H2O)n(OH)]+ species located in the exchange positions of the materials with little or no contribution of ZnO or metallic Zn. The effect of Zn/Al ratio on their catalytic performance in methanol conversion to aromatics has been investigated. In all cases, higher Zn content causes an increase in the yield of aromatics while keeping the production of alkanes low. For similar Zn contents, high densities of Al sites favour the hydrogen transfer reactions and alkane formation whereas in samples with low Al contents, and thus higher Zn/Al ratio, the dehydrogenation reactions in which molecular hydrogen is released are favoured.
dc.languageEN
dc.publisherAcademic Press
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 International
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 International
dc.rights.urihttps://creativecommons.org/licenses/by-nc-nd/4.0/
dc.rights.urihttps://creativecommons.org/licenses/by-nc-nd/4.0/
dc.titleHigh Zn/Al ratios enhance dehydrogenation vs hydrogen transfer reactions of Zn-ZSM-5 catalytic systems in methanol conversion to aromatics
dc.typeJournal article
dc.creator.authorPinilla-Herrero, Irene
dc.creator.authorBorfecchia, Elisa
dc.creator.authorHolzinger, Julian
dc.creator.authorMentzel, Uffe V.
dc.creator.authorJoensen, Finn
dc.creator.authorLomachenko, Kirill A.
dc.creator.authorBordiga, Silvia
dc.creator.authorLamberti, Carlo
dc.creator.authorBerlier, Gloria
dc.creator.authorOlsbye, Unni
dc.creator.authorSvelle, Stian
dc.creator.authorSkibsted, Jørgen
dc.creator.authorBeato, Pablo
cristin.unitcode185,15,12,54
cristin.unitnameKatalyse
cristin.ispublishedtrue
cristin.fulltextpostprint
cristin.qualitycode2
dc.identifier.cristin1597396
dc.identifier.bibliographiccitationinfo:ofi/fmt:kev:mtx:ctx&ctx_ver=Z39.88-2004&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.jtitle=Journal of Catalysis&rft.volume=362&rft.spage=146&rft.date=2018
dc.identifier.jtitleJournal of Catalysis
dc.identifier.volume362
dc.identifier.startpage146
dc.identifier.endpage163
dc.identifier.doihttps://doi.org/10.1016/j.jcat.2018.03.032
dc.identifier.urnURN:NBN:no-76143
dc.type.documentTidsskriftartikkel
dc.type.peerreviewedPeer reviewed
dc.source.issn0021-9517
dc.identifier.fulltextFulltext https://www.duo.uio.no/bitstream/handle/10852/72985/1/deponert97948.pdf
dc.type.versionAcceptedVersion


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Attribution-NonCommercial-NoDerivatives 4.0 International
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Attribution-NonCommercial-NoDerivatives 4.0 International
This item's license is: Attribution-NonCommercial-NoDerivatives 4.0 International