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dc.date.accessioned2018-09-11T10:10:40Z
dc.date.available2018-10-23T22:31:40Z
dc.date.created2017-11-14T14:21:30Z
dc.date.issued2017
dc.identifier.citationRojo-Gama, Daniel Nielsen, Malte Wragg, David Dyballa, Michael Martin Holzinger, Julian Falsig, Hanne Lundegaard, Lars Fahl Beato, Pablo Brogaard, Rasmus Yding Lillerud, Karl Petter Olsbye, Unni Svelle, Stian . A Straightforward Descriptor for the Deactivation of Zeolite Catalyst H-ZSM-5. ACS Catalysis. 2017, 7(12), 8235-8246
dc.identifier.urihttp://hdl.handle.net/10852/64608
dc.description.abstractZSM-5 is a widely used zeolite catalyst and is employed industrially for the methanol to gasoline (MTG) process. Even so, deactivation of ZSM-5 by coke formation constitutes a major technical and also fundamental challenge. We investigate the deactivation of a range of ZSM-5 catalysts through catalytic testing, physicochemical characterization, and powder X-ray diffraction (XRD). It is demonstrated that the unit cell changes upon deactivation. Periodic density functional theory is used to show that the change is induced by certain methyl substituted benzenes in the channel intersection in ZSM-5. This finding is corroborated by Rietveld refinement of XRD data obtained for deactivated catalysts. We are able to establish a direct correlation between the difference in the length of the a- and b-unit cell vectors and the total amount of coke, the remaining acidity, and the remaining surface area of the catalysts. This a- minus b-parameter is a straightforward descriptor that carries the essential information regarding the degree of deactivation of a ZSM-5 catalyst, and a routine measurement of a diffractogram of the catalyst can be used to quantitatively assess the degree of deactivation.en_US
dc.languageEN
dc.publisherAmerican Chemical Society
dc.titleA Straightforward Descriptor for the Deactivation of Zeolite Catalyst H-ZSM-5en_US
dc.typeJournal articleen_US
dc.creator.authorRojo-Gama, Daniel
dc.creator.authorNielsen, Malte
dc.creator.authorWragg, David
dc.creator.authorDyballa, Michael Martin
dc.creator.authorHolzinger, Julian
dc.creator.authorFalsig, Hanne
dc.creator.authorLundegaard, Lars Fahl
dc.creator.authorBeato, Pablo
dc.creator.authorBrogaard, Rasmus Yding
dc.creator.authorLillerud, Karl Petter
dc.creator.authorOlsbye, Unni
dc.creator.authorSvelle, Stian
cristin.unitcode185,15,0,0
cristin.unitnameDet matematisk-naturvitenskapelige fakultet
cristin.ispublishedtrue
cristin.fulltextpostprint
cristin.qualitycode1
dc.identifier.cristin1514017
dc.identifier.bibliographiccitationinfo:ofi/fmt:kev:mtx:ctx&ctx_ver=Z39.88-2004&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.jtitle=ACS Catalysis&rft.volume=7&rft.spage=8235&rft.date=2017
dc.identifier.jtitleACS Catalysis
dc.identifier.volume7
dc.identifier.issue12
dc.identifier.startpage8235
dc.identifier.endpage8246
dc.identifier.doihttp://dx.doi.org/10.1021/acscatal.7b02193
dc.identifier.urnURN:NBN:no-67145
dc.type.documentTidsskriftartikkelen_US
dc.type.peerreviewedPeer reviewed
dc.source.issn2155-5435
dc.identifier.fulltextFulltext https://www.duo.uio.no/bitstream/handle/10852/64608/2/Manuscript_JCatal24854.pdf
dc.type.versionAcceptedVersion
dc.relation.projectNOTUR/NORSTORE/NN4683K
dc.relation.projectNFR/237080
dc.relation.projectEC/FP7/606965


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