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dc.contributor.authorPeng, Chong
dc.contributor.authorGuo, Rong
dc.contributor.authorFeng, Xiang
dc.contributor.authorFang, Xiangchen
dc.date.accessioned2019-03-20T13:19:34Z
dc.date.available2019-03-20T13:19:34Z
dc.date.created2018-11-22T14:16:06Z
dc.date.issued2018
dc.identifier.issn1385-8947
dc.identifier.urihttp://hdl.handle.net/11250/2590872
dc.description.abstractEver-increasing concern on environmental impacts (e.g., sulfur pollution) by fossil fuels has triggered the research on hydrodesulfurization (HDS). In this work, Co-Mo nanoparticles were deposited on the mesoporous γ-Al2O3 support with the addition of organic compound, and the physico-chemical properties of the catalysts (Co-Mo-C/mesoporous γ-Al2O3) were then characterized by multi-techniques such as H2-TPR, HRTEM, XPS, N2 physisorption. It is found that the Co-Mo-C/mesoporous γ-Al2O3 catalyst is easier to be reduced when organic compound is added, enhancing the sulfuration. This results in better dispersion of Co-Mo-S species and more Co-Mo-S II active sites, which significantly enhance diesel ultra-deep hydrodesulfurization activity. Furthermore, this novel catalyst was also tested for HDS reaction in a 3000 kt/a industrial-scale plant. Gratifyingly, this catalyst showed effective reduction of sulfur content from 9000 to less than 10 μg/g and also high stability over 5000 h. The results are of great significance to the design and development of industrial HDS catalysts.nb_NO
dc.language.isoengnb_NO
dc.publisherElseviernb_NO
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 Internasjonal*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/deed.no*
dc.titleTailoring the structure of Co-Mo/mesoporous γ-Al2O3 catalysts by adding multi-hydroxyl compound: A 3000 kt/a industrial-scale diesel ultra-deep hydrodesulfurization studynb_NO
dc.typeJournal articlenb_NO
dc.typePeer reviewednb_NO
dc.description.versionacceptedVersionnb_NO
dc.source.journalChemical Engineering Journalnb_NO
dc.identifier.doi10.1016/j.cej.2018.08.092
dc.identifier.cristin1633813
dc.description.localcode© 2018. This is the authors’ accepted and refereed manuscript to the article. Locked until 14 August 2020 due to copyright restrictions. This manuscript version is made available under the CC-BY-NC-ND 4.0 license http://creativecommons.org/licenses/by-nc-nd/4.0/nb_NO
cristin.unitcode194,66,30,0
cristin.unitnameInstitutt for kjemisk prosessteknologi
cristin.ispublishedtrue
cristin.fulltextpostprint
cristin.qualitycode1


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Attribution-NonCommercial-NoDerivatives 4.0 Internasjonal
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