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dc.contributor.authorRytter, Erling
dc.contributor.authorSalman, Ata ul Rauf
dc.contributor.authorTsakoumis, Nikolaos
dc.contributor.authorMyrstad, Rune
dc.contributor.authorYang, Jia
dc.contributor.authorLögdberg, Sara
dc.contributor.authorHolmen, Anders
dc.contributor.authorRønning, Magnus
dc.date.accessioned2017-12-05T10:06:49Z
dc.date.available2017-12-05T10:06:49Z
dc.date.created2017-12-04T08:52:54Z
dc.date.issued2018
dc.identifier.citationCatalysis Today. 2018, 299 20-27.nb_NO
dc.identifier.issn0920-5861
dc.identifier.urihttp://hdl.handle.net/11250/2469223
dc.description.abstractEight different silanes with chloro or methoxy active ligands have been examined to modify the surface of a standard γ-alumina support to investigate the effect of surface acidity and hydrophobicity in Fischer-Tropsch synthesis (FTS) at common operating conditions (210 °C; 20 bar; H2/CO = 2.1). Silanes were impregnated prior to cobalt (Pre) or after cobalt impregnation and calcination (Post). Samples were characterized by standard techniques (FTIR, XRD, TPD, TPR, TGA, BET). In the Post series, cobalt crystallite size is maintained, while it is reduced when cobalt impregnation is performed on a partly hydrophobic surface. Both series of catalysts have FTS performances that deviate significantly from a reference catalyst and, in combination with characterization data, the silanes have modified all the 15 examined catalysts. The Pre series offer options for improved selectivity to higher hydrocarbons in FTS. The effects of silylation on FT performance mechanisms are discussed in terms of gas diffusion limitations, strain in cobalt particles and partial blocking of CO activation sites.nb_NO
dc.language.isoengnb_NO
dc.publisherElseviernb_NO
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 Internasjonal*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/deed.no*
dc.titleHydrophobic Catalyst Support Surfaces by Silylation of γ-Alumina for Co/Re Fischer-Tropsch Synthesisnb_NO
dc.typeJournal articlenb_NO
dc.typePeer reviewednb_NO
dc.description.versionacceptedVersionnb_NO
dc.source.pagenumber20-27nb_NO
dc.source.volume299nb_NO
dc.source.journalCatalysis Todaynb_NO
dc.identifier.doi10.1016/j.cattod.2017.04.031
dc.identifier.cristin1522220
dc.relation.projectNorges forskningsråd: 174893nb_NO
dc.description.localcode© 2017. This is the authors’ accepted and refereed manuscript to the article. LOCKED until 3.5.2019 due to copyright restrictions. This manuscript version is made available under the CC-BY-NC-ND 4.0 license http://creativecommons.org/licenses/by-nc-nd/4.0/nb_NO
cristin.unitcode194,66,30,0
cristin.unitnameInstitutt for kjemisk prosessteknologi
cristin.ispublishedtrue
cristin.fulltextpostprint
cristin.qualitycode2


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Attribution-NonCommercial-NoDerivatives 4.0 Internasjonal
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