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dc.contributor.authorDuan, Xuezhi
dc.contributor.authorZhang, Yanfang
dc.contributor.authorPan, Minjian
dc.contributor.authorDong, Hua
dc.contributor.authorChen, Bingxu
dc.contributor.authorMa, Yuanyuan
dc.contributor.authorQian, Gang
dc.contributor.authorZhou, Xinggui
dc.contributor.authorYang, Jia
dc.contributor.authorChen, De
dc.date.accessioned2019-03-22T09:28:19Z
dc.date.available2019-03-22T09:28:19Z
dc.date.created2018-12-15T16:43:05Z
dc.date.issued2018
dc.identifier.citationAIChE Journal. 2018, 64 (11), 3979-3987.nb_NO
dc.identifier.issn0001-1541
dc.identifier.urihttp://hdl.handle.net/11250/2591245
dc.description.abstractUnderstanding of selective base‐free oxidation of glycerol to dihydroxyacetone (DHA) over Pt‐based catalysts is of paramount scientific and industrial importance. In this work, a comparative study between differently sized SbOx‐promoted and unpromoted Pt/CNTs catalysts is carried out to decouple the promoter effects from the metal size effects. The introduction of SbOx appears to enhance both the glycerol oxidation activity and the DHA selectivity, and the largely sized promoted Pt/CNTs catalysts afford a relatively high DHA yield and less C–C bond cleavage. X‐ray photoelectron spectroscopy measurements reveal that the Sb species are mainly in the form of SbOx, and the differently sized promoted catalysts show similar metal binding energies. Furthermore, theoretical studies on the promotional effects of SbOx are carried out by DFT calculations. It is found that the presence of the promoter on the catalyst surface favors the preferential activation of the secondary hydroxyl group.nb_NO
dc.language.isoengnb_NO
dc.publisherWileynb_NO
dc.titleSbOx‐promoted pt nanoparticles supported on CNTs as catalysts for base‐free oxidation of glycerol to dihydroxyacetonenb_NO
dc.typeJournal articlenb_NO
dc.typePeer reviewednb_NO
dc.description.versionacceptedVersionnb_NO
dc.source.pagenumber3979-3987nb_NO
dc.source.volume64nb_NO
dc.source.journalAIChE Journalnb_NO
dc.source.issue11nb_NO
dc.identifier.doi10.1002/aic.16217
dc.identifier.cristin1643681
dc.description.localcode© 2018 American Institute of Chemical Engineers. Locked until 19 June 2019 due to copyright restrictions. This is the peer reviewed version of an article, which has been published in final form at https://doi.org/10.1002/aic.16217. This article may be used for non-commercial purposes in accordance with Wiley Terms and Conditions for Self-Archiving.nb_NO
cristin.unitcode194,66,30,0
cristin.unitnameInstitutt for kjemisk prosessteknologi
cristin.ispublishedtrue
cristin.fulltextpostprint
cristin.qualitycode2


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