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dc.contributor.authorWang, Haizhi
dc.contributor.authorSun, Lili
dc.contributor.authorSui, Zhi Jun
dc.contributor.authorZhu, Yi-an
dc.contributor.authorYe, Guanghua
dc.contributor.authorChen, De
dc.contributor.authorZhou, Xing-Gui
dc.contributor.authorYuan, Wei-kang
dc.date.accessioned2019-06-03T14:19:14Z
dc.date.available2019-06-03T14:19:14Z
dc.date.created2018-12-15T17:47:01Z
dc.date.issued2018
dc.identifier.citationIndustrial & Engineering Chemistry Research. 2018, 57 (26), 8647-8654.nb_NO
dc.identifier.issn0888-5885
dc.identifier.urihttp://hdl.handle.net/11250/2599773
dc.description.abstractCatalyst deactivation by coking is one major problem for propane dehydrogenation (PDH). To develop catalysts with high resistance to coke, the analysis of coke becomes essential. In this work, an analysis procedure is proposed and validated to acquire the detailed locations and compositions of the coke formed on an as-synthesized Pt–Sn/Al2O3 catalyst. This procedure combines high-resolution transmission electron microscopy (HRTEM), FT-IR, Raman, thermogravimetric analysis (TG), and pyrolysis GC-MS; with this procedure, the systematic and quantitative analysis of coke can be achieved. The results show that the coke is located on the metal, in the vicinity of the metal, and on the support. Besides, aliphatics, aromatics, and pregraphite cokes are identified, and they account for 69.0, 4.4, and 26.6 wt %, respectively. Finally, an in situ DRIFT study is performed, and the results show that the aliphatic coke can be transformed into the aromatic coke and this transformation is related to the deep dehydrogenation reactions.nb_NO
dc.language.isoengnb_NO
dc.publisherAmerican Chemical Societynb_NO
dc.titleCoke Formation on Pt–Sn/Al2O3 Catalyst for Propane Dehydrogenationnb_NO
dc.typeJournal articlenb_NO
dc.typePeer reviewednb_NO
dc.description.versionacceptedVersionnb_NO
dc.source.pagenumber8647-8654nb_NO
dc.source.volume57nb_NO
dc.source.journalIndustrial & Engineering Chemistry Researchnb_NO
dc.source.issue26nb_NO
dc.identifier.doi10.1021/acs.iecr.8b01313
dc.identifier.cristin1643685
dc.description.localcode© American Chemical Society 2018. This is the authors accepted and refereed manuscript to the article. Locked until 8.6.2019 due to copyright restrictions.nb_NO
cristin.unitcode194,66,30,0
cristin.unitnameInstitutt for kjemisk prosessteknologi
cristin.ispublishedtrue
cristin.fulltextoriginal
cristin.qualitycode2


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