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dc.contributor.authorRadstake, Paul B.
dc.contributor.authorRønning, Magnus
dc.contributor.authorHolmen, Anders
dc.date.accessioned2018-04-05T06:58:46Z
dc.date.available2018-04-05T06:58:46Z
dc.date.created2018-04-03T11:58:41Z
dc.date.issued2018
dc.identifier.citationCatalysis Letters. 2018, 148 1055-1066.nb_NO
dc.identifier.issn1011-372X
dc.identifier.urihttp://hdl.handle.net/11250/2492696
dc.description.abstractThe oxygen-assisted dehydrogenation of ethane at 650 °C shows that adding Sn to the Pt catalyst results in increased conversion and selectivity to ethylene. Even the smallest amount of tin (0.16 wt%) has a significant effect. The addition of tin also increases the stability of the Pt/Al2O3 catalyst, in particular it reduces the amount of carbon or carbonaceous species. Adding hydrogen to the feed had a remarkable effect on the selectivity, but the conversion of ethane was almost unaffected for Pt–Sn catalysts. The selectivity to ethylene increased substantially and the selectivity to CO/CO2 decreased even for the smallest amount of tin used. Unexpected values for the selectivity to other compounds were also observed, in particular for the selectivity to acetylene. The importance of possible Pt–Sn alloys or the necessity of contact between Pt and Sn was studied using a physical mixture of Pt/Al2O3 and Sn/Al2O3. However, almost the same effect was obtained by using the physical mixture as with the co-impregnated sample, i.e. the Pt–Sn catalysts.nb_NO
dc.language.isoengnb_NO
dc.publisherSpringer Verlagnb_NO
dc.titleInfluence of H2 on the Oxygen-Assisted Dehydrogenation of Ethane over Al2O3-supported Pt–Sn Catalystsnb_NO
dc.typeJournal articlenb_NO
dc.typePeer reviewednb_NO
dc.description.versionacceptedVersionnb_NO
dc.source.pagenumber1055-1066nb_NO
dc.source.volume148nb_NO
dc.source.journalCatalysis Lettersnb_NO
dc.identifier.doi10.1007/s10562-018-2334-3
dc.identifier.cristin1576771
dc.relation.projectNorges forskningsråd: 182531nb_NO
dc.description.localcodeThis is a post-peer-review, pre-copyedit version of an article published in [Catalysis Letters] Locked until 23.2.2019 due to copyright restrictions. The final authenticated version is available online at: https://link.springer.com/article/10.1007%2Fs10562-018-2334-3nb_NO
cristin.unitcode194,66,30,0
cristin.unitnameInstitutt for kjemisk prosessteknologi
cristin.ispublishedtrue
cristin.fulltextpostprint
cristin.qualitycode1


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