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dc.contributor.authorTsakoumis, Nikolaos
dc.contributor.authorDehghan-Niri, Roya
dc.contributor.authorRønning, Magnus
dc.contributor.authorWalmsley, John
dc.contributor.authorBorg, Øyvind
dc.contributor.authorRytter, Erling
dc.contributor.authorHolmen, Anders
dc.date.accessioned2022-08-10T09:21:59Z
dc.date.available2022-08-10T09:21:59Z
dc.date.created2014-06-16T13:50:57Z
dc.date.issued2014
dc.identifier.citationApplied Catalysis A : General. 2014, 479 59-69.en_US
dc.identifier.issn0926-860X
dc.identifier.urihttps://hdl.handle.net/11250/3011048
dc.description.abstractCalcined, reduced and spent Co-Re/γ-Al2O3 catalysts for Fischer–Tropsch synthesis (FTS) were characterized and compared. Co-K-edge and Re-LIII-edge X-ray absorption near edge structure (XANES), X-ray powder diffraction (XRPD), transmission electron microscopy (TEM) and H2 chemisorption were used to provide insight into structural transformations that the catalyst experiences during a month of operation in a semi-commercial FTS plant. Results from the core techniques for nanoparticle size determination suggest that sintering of the cobalt crystallites is an important deactivation mechanism in FTS performed in slurry reactors. In addition, a higher degree of reduction is observed for the spent catalytic material, while Re appears in a partially reduced state before and after reaction. The particle size distribution together with the spread of Co nanoparticles on the γ-Al2O3 surface indicates crystallite migration as the prevailing mechanism.en_US
dc.language.isoengen_US
dc.publisherElsevieren_US
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 Internasjonal*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/deed.no*
dc.titleX-ray absorption, X-ray diffraction and electron microscopy study of spent cobalt based catalyst in semi-commercial scale Fischer-Tropsch synthesisen_US
dc.typePeer revieweden_US
dc.typeJournal articleen_US
dc.description.versionacceptedVersionen_US
dc.source.pagenumber59-69en_US
dc.source.volume479en_US
dc.source.journalApplied Catalysis A : Generalen_US
dc.identifier.doi10.1016/j.apcata.2014.03.035
dc.identifier.cristin1138302
cristin.ispublishedtrue
cristin.fulltextpostprint
cristin.qualitycode1


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Attribution-NonCommercial-NoDerivatives 4.0 Internasjonal
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