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dc.contributor.authorLei, Jiaqi
dc.contributor.authorDong, Hua
dc.contributor.authorDuan, Xuezhi
dc.contributor.authorChen, Wenyao
dc.contributor.authorQian, Gang
dc.contributor.authorChen, De
dc.contributor.authorZhou, Xinggui
dc.date.accessioned2018-05-08T11:49:05Z
dc.date.available2018-05-08T11:49:05Z
dc.date.created2016-09-14T21:19:25Z
dc.date.issued2016
dc.identifier.citationIndustrial & Engineering Chemistry Research. 2016, 55 (2), 420-427.nb_NO
dc.identifier.issn0888-5885
dc.identifier.urihttp://hdl.handle.net/11250/2497583
dc.description.abstractTwo kinds of activated carbon (AC)-supported Pt catalysts with similar particle sizes were respectively synthesized using the polyol method and incipient wetness impregnation method, and then tested for glycerol oxidation in a base-free condition. It is revealed that the initial reaction rate on the Pt catalyst prepared by the polyol method (Pt/ACPO) is nearly triple that on the Pt catalyst prepared by incipient wetness impregnation method (Pt/ACIWI), and the Pt/ACIWI catalyst favors further oxidation of glyceraldehyde to glyceric acid and more C–C bond cleavage, which might mainly arise from the difference in relative coverage of oxygen to glycerol caused by the different electronic properties of Pt as well as the difference in the catalyst surface properties. Moreover, the deactivation mechanisms of both catalysts were also investigated. The results show that strongly adsorbed intermediates contribute significantly to the deactivation of the Pt/ACPO catalyst, while both the oxygen poison and the adsorption of intermediates on Pt surfaces cause the deactivation of the Pt/ACIWI catalyst.nb_NO
dc.language.isoengnb_NO
dc.publisherAmerican Chemical Societynb_NO
dc.titleInsights into Activated Carbon-Supported Platinum Catalysts for Base-Free Oxidation of Glycerolnb_NO
dc.typeJournal articlenb_NO
dc.typePeer reviewednb_NO
dc.description.versionpublishedVersionnb_NO
dc.source.pagenumber420-427nb_NO
dc.source.volume55nb_NO
dc.source.journalIndustrial & Engineering Chemistry Researchnb_NO
dc.source.issue2nb_NO
dc.identifier.doi10.1021/acs.iecr.5b03076
dc.identifier.cristin1381503
dc.relation.projectNorges forskningsråd: 243749nb_NO
dc.description.localcodeThis article will not be available due to copyright restrictions (c) 2016 by American Chemical Societynb_NO
cristin.unitcode194,66,30,0
cristin.unitnameInstitutt for kjemisk prosessteknologi
cristin.ispublishedtrue
cristin.fulltextoriginal
cristin.qualitycode2


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