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dc.contributor.authorQi, Yanying
dc.contributor.authorYang, Jia
dc.contributor.authorChen, De
dc.contributor.authorHolmen, Anders
dc.date.accessioned2018-05-08T12:02:01Z
dc.date.available2018-05-08T12:02:01Z
dc.date.created2015-01-09T12:41:24Z
dc.date.issued2015
dc.identifier.citationCatalysis Letters. 2015, 145 (1), 145-161.nb_NO
dc.identifier.issn1011-372X
dc.identifier.urihttp://hdl.handle.net/11250/2497591
dc.description.abstractDuring the last years it has been an increasing focus on fundamental studies of the Fischer–Tropsch synthesis (FTS). Steady-state isotopic transient kinetic analysis and first principles investigation have proven to be important methods in studying the reaction mechanism of FTS. The present contribution deals with recent progresses in understanding of the F–T mechanism on Co catalysts based on combined DFT calculations, in situ characterization, steady-state isotopic transient kinetic analysis and microkinetics. A brief outlook into future perspectives of the FTS for converting synthesis gas from different carbon sources to fuels and chemicals is also provided.nb_NO
dc.language.isoengnb_NO
dc.publisherSpringer Verlagnb_NO
dc.titleRecent Progresses in Understanding of Co-Based Fischer–Tropsch Catalysis by Means of Transient Kinetic Studies and Theoretical Analysisnb_NO
dc.typeJournal articlenb_NO
dc.typePeer reviewednb_NO
dc.description.versionpublishedVersionnb_NO
dc.source.pagenumber145-161nb_NO
dc.source.volume145nb_NO
dc.source.journalCatalysis Lettersnb_NO
dc.source.issue1nb_NO
dc.identifier.doi10.1007/s10562-014-1419-x
dc.identifier.cristin1193974
dc.relation.projectNorges forskningsråd: 209337nb_NO
dc.description.localcodeThis article will not be available due to copyright restrictions (c) 2014 by Springer Verlagnb_NO
cristin.unitcode194,66,30,0
cristin.unitnameInstitutt for kjemisk prosessteknologi
cristin.ispublishedtrue
cristin.fulltextoriginal
cristin.qualitycode1


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