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dc.contributor.authorWang, Hai-Zhi
dc.contributor.authorZhang, Wei
dc.contributor.authorJiang, Jia-Wei
dc.contributor.authorSui, Zhi-Jun
dc.contributor.authorZhu, Yi-An
dc.contributor.authorYe, Guang-Hua
dc.contributor.authorChen, De
dc.contributor.authorZhou, Xing-Gui
dc.contributor.authorYuan, Wei-Kang
dc.date.accessioned2020-01-28T13:48:49Z
dc.date.available2020-01-28T13:48:49Z
dc.date.created2019-05-28T13:38:57Z
dc.date.issued2019
dc.identifier.citationCatalysis science & technology. 2019, 9 (3), 867-876.nb_NO
dc.identifier.issn2044-4753
dc.identifier.urihttp://hdl.handle.net/11250/2638394
dc.description.abstractIntroducing sulfur species into Pt catalysts has been proven to be an effective method to improve their performance in various reactions. However, the role of sulfur addition on Pt catalysts catalyzing propane dehydrogenation (PDH) is still not clear. This work combines catalyst characterizations, catalytic kinetics studies and DFT calculations to understand the influence of H2S addition in the feed on Pt/θ-Al2O3 catalyzed PDH from a mechanistic perspective. With the addition of a trace amount of H2S in the feed (3 ppm), the propylene selectivity increases from 79% to 96% and the deactivation factor decreases from 33% to 18%, at the expense of a slight activity loss. The improved catalytic performance can be partially attributed to the electron transfer from sulfur species to Pt atoms as indicated by CO-DRIFTS results. DFT calculations show that H2S could be the dominating sulfur species on Pt particles and donate electrons to Pt atoms, which further proves that sulfur species improve the catalytic performance by donating electrons. In addition, the repulsion between sulfur species and C3 hydrocarbons also explains the improved catalytic performance.nb_NO
dc.language.isoengnb_NO
dc.publisherRoyal Society of Chemistrynb_NO
dc.titleThe role of H2S addition on Pt/Al2O3 catalyzed propane dehydrogenation: a mechanistic studynb_NO
dc.typeJournal articlenb_NO
dc.typePeer reviewednb_NO
dc.description.versionacceptedVersionnb_NO
dc.source.pagenumber867-876nb_NO
dc.source.volume9nb_NO
dc.source.journalCatalysis science & technologynb_NO
dc.source.issue3nb_NO
dc.identifier.doi10.1039/c8cy02393j
dc.identifier.cristin1700882
dc.description.localcode© 2019. This is the authors' accepted and refereed manuscript to the article. The final authenticated version is available online at: https://doi.org/10.1039/C8CY02393Jnb_NO
cristin.unitcode194,66,30,0
cristin.unitnameInstitutt for kjemisk prosessteknologi
cristin.ispublishedtrue
cristin.fulltextpostprint
cristin.qualitycode0


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