dc.contributor.author | Peng, Chong | |
dc.contributor.author | Guo, Rong | |
dc.contributor.author | Feng, Xiang | |
dc.contributor.author | Fang, Xiangchen | |
dc.date.accessioned | 2019-03-20T13:19:34Z | |
dc.date.available | 2019-03-20T13:19:34Z | |
dc.date.created | 2018-11-22T14:16:06Z | |
dc.date.issued | 2018 | |
dc.identifier.issn | 1385-8947 | |
dc.identifier.uri | http://hdl.handle.net/11250/2590872 | |
dc.description.abstract | Ever-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.iso | eng | nb_NO |
dc.publisher | Elsevier | nb_NO |
dc.rights | Attribution-NonCommercial-NoDerivatives 4.0 Internasjonal | * |
dc.rights.uri | http://creativecommons.org/licenses/by-nc-nd/4.0/deed.no | * |
dc.title | Tailoring the structure of Co-Mo/mesoporous γ-Al2O3 catalysts by adding multi-hydroxyl compound: A 3000 kt/a industrial-scale diesel ultra-deep hydrodesulfurization study | nb_NO |
dc.type | Journal article | nb_NO |
dc.type | Peer reviewed | nb_NO |
dc.description.version | acceptedVersion | nb_NO |
dc.source.journal | Chemical Engineering Journal | nb_NO |
dc.identifier.doi | 10.1016/j.cej.2018.08.092 | |
dc.identifier.cristin | 1633813 | |
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.unitcode | 194,66,30,0 | |
cristin.unitname | Institutt for kjemisk prosessteknologi | |
cristin.ispublished | true | |
cristin.fulltext | postprint | |
cristin.qualitycode | 1 | |