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Hydro-treating of Asphaltenes in Supercritical Toluene with MgO-Supported Fe, Ni, NiMo, and CoMo Catalysts
For the first time, the AVTB-derived asphaltenes (containing very high concentrations of sulfur (7.70 wt % S) and nitrogen (1.08 wt % N)) were hydrotreated over novel MgO-supported Fe, Ni, NiMo, and CoMo catalysts in supercritical toluene at 380 °C under hydrogen of 5 MPa (cold pressure) in a batch...
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Published in: | Energy & fuels 2009-07, Vol.23 (7), p.3645-3651 |
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creator | Xu, Chunbao (Charles) Su, Huasu Ghosh, Mainak |
description | For the first time, the AVTB-derived asphaltenes (containing very high concentrations of sulfur (7.70 wt % S) and nitrogen (1.08 wt % N)) were hydrotreated over novel MgO-supported Fe, Ni, NiMo, and CoMo catalysts in supercritical toluene at 380 °C under hydrogen of 5 MPa (cold pressure) in a batch reactor. The supercritical toluene alone without any catalyst was found to be effective for conversion of the highly aromatic asphaltenes (AS) to less aromatic maltenes (MA) through a thermal cracking mechanism. All the MgO-supported catalysts proved to be effective for hydro-conversion of AS to MA in supercritical toluene. The activities of these catalysts for AS conversion showed the order of sequence of Fe/MgO < Ni/MgO < CoMo/MgO < NiMo/MgO. Among all the MgO-supported catalysts tested, NiMo/MgO was found to be the most active one for promoting the removal of sulfur and AS. The sulfur/nitrogen/AS removal efficiencies for the NiMo/MgO catalyst increased with the treatment time, and the efficiencies at 120 min of treatment attained as high as 43%, 30%, and 70%, respectively. The MgO-supported catalysts showed excellent performance for preventing and retarding the formation of highly condensed aromatics or coke in the hydro-treatment of AS in supercritical toluene. With the presence of NiMo/MgO catalyst, hydro-treating AS in the supercritical toluene for a reaction time up to 120 min produced a strikingly low yield ( |
doi_str_mv | 10.1021/ef900126v |
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The supercritical toluene alone without any catalyst was found to be effective for conversion of the highly aromatic asphaltenes (AS) to less aromatic maltenes (MA) through a thermal cracking mechanism. All the MgO-supported catalysts proved to be effective for hydro-conversion of AS to MA in supercritical toluene. The activities of these catalysts for AS conversion showed the order of sequence of Fe/MgO < Ni/MgO < CoMo/MgO < NiMo/MgO. Among all the MgO-supported catalysts tested, NiMo/MgO was found to be the most active one for promoting the removal of sulfur and AS. The sulfur/nitrogen/AS removal efficiencies for the NiMo/MgO catalyst increased with the treatment time, and the efficiencies at 120 min of treatment attained as high as 43%, 30%, and 70%, respectively. The MgO-supported catalysts showed excellent performance for preventing and retarding the formation of highly condensed aromatics or coke in the hydro-treatment of AS in supercritical toluene. With the presence of NiMo/MgO catalyst, hydro-treating AS in the supercritical toluene for a reaction time up to 120 min produced a strikingly low yield (<0.7%) of toluene-insoluble product.</description><identifier>ISSN: 0887-0624</identifier><identifier>EISSN: 1520-5029</identifier><identifier>DOI: 10.1021/ef900126v</identifier><identifier>CODEN: ENFUEM</identifier><language>eng</language><publisher>Washington, DC: American Chemical Society</publisher><subject>Applied sciences ; Crude oil, natural gas and petroleum products ; Energy ; Exact sciences and technology ; Fossil Fuels ; Fuels ; Processing of crude oil and oils from shales and tar sands. Processes. Equipment. Refinery and treatment units</subject><ispartof>Energy & fuels, 2009-07, Vol.23 (7), p.3645-3651</ispartof><rights>Copyright © 2009 American Chemical Society</rights><rights>2015 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-a326t-c68e30a52360ec8c3557e3c1003759fa40bc783eb62cabee79a2219d4e728baf3</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>309,310,314,780,784,789,790,23930,23931,25140,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=22082262$$DView record in Pascal Francis$$Hfree_for_read</backlink></links><search><creatorcontrib>Xu, Chunbao (Charles)</creatorcontrib><creatorcontrib>Su, Huasu</creatorcontrib><creatorcontrib>Ghosh, Mainak</creatorcontrib><title>Hydro-treating of Asphaltenes in Supercritical Toluene with MgO-Supported Fe, Ni, NiMo, and CoMo Catalysts</title><title>Energy & fuels</title><addtitle>Energy Fuels</addtitle><description>For the first time, the AVTB-derived asphaltenes (containing very high concentrations of sulfur (7.70 wt % S) and nitrogen (1.08 wt % N)) were hydrotreated over novel MgO-supported Fe, Ni, NiMo, and CoMo catalysts in supercritical toluene at 380 °C under hydrogen of 5 MPa (cold pressure) in a batch reactor. The supercritical toluene alone without any catalyst was found to be effective for conversion of the highly aromatic asphaltenes (AS) to less aromatic maltenes (MA) through a thermal cracking mechanism. All the MgO-supported catalysts proved to be effective for hydro-conversion of AS to MA in supercritical toluene. The activities of these catalysts for AS conversion showed the order of sequence of Fe/MgO < Ni/MgO < CoMo/MgO < NiMo/MgO. Among all the MgO-supported catalysts tested, NiMo/MgO was found to be the most active one for promoting the removal of sulfur and AS. The sulfur/nitrogen/AS removal efficiencies for the NiMo/MgO catalyst increased with the treatment time, and the efficiencies at 120 min of treatment attained as high as 43%, 30%, and 70%, respectively. The MgO-supported catalysts showed excellent performance for preventing and retarding the formation of highly condensed aromatics or coke in the hydro-treatment of AS in supercritical toluene. With the presence of NiMo/MgO catalyst, hydro-treating AS in the supercritical toluene for a reaction time up to 120 min produced a strikingly low yield (<0.7%) of toluene-insoluble product.</description><subject>Applied sciences</subject><subject>Crude oil, natural gas and petroleum products</subject><subject>Energy</subject><subject>Exact sciences and technology</subject><subject>Fossil Fuels</subject><subject>Fuels</subject><subject>Processing of crude oil and oils from shales and tar sands. Processes. Equipment. 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Processes. Equipment. Refinery and treatment units</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Xu, Chunbao (Charles)</creatorcontrib><creatorcontrib>Su, Huasu</creatorcontrib><creatorcontrib>Ghosh, Mainak</creatorcontrib><collection>Pascal-Francis</collection><collection>CrossRef</collection><jtitle>Energy & fuels</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Xu, Chunbao (Charles)</au><au>Su, Huasu</au><au>Ghosh, Mainak</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Hydro-treating of Asphaltenes in Supercritical Toluene with MgO-Supported Fe, Ni, NiMo, and CoMo Catalysts</atitle><jtitle>Energy & fuels</jtitle><addtitle>Energy Fuels</addtitle><date>2009-07-16</date><risdate>2009</risdate><volume>23</volume><issue>7</issue><spage>3645</spage><epage>3651</epage><pages>3645-3651</pages><issn>0887-0624</issn><eissn>1520-5029</eissn><coden>ENFUEM</coden><abstract>For the first time, the AVTB-derived asphaltenes (containing very high concentrations of sulfur (7.70 wt % S) and nitrogen (1.08 wt % N)) were hydrotreated over novel MgO-supported Fe, Ni, NiMo, and CoMo catalysts in supercritical toluene at 380 °C under hydrogen of 5 MPa (cold pressure) in a batch reactor. The supercritical toluene alone without any catalyst was found to be effective for conversion of the highly aromatic asphaltenes (AS) to less aromatic maltenes (MA) through a thermal cracking mechanism. All the MgO-supported catalysts proved to be effective for hydro-conversion of AS to MA in supercritical toluene. The activities of these catalysts for AS conversion showed the order of sequence of Fe/MgO < Ni/MgO < CoMo/MgO < NiMo/MgO. Among all the MgO-supported catalysts tested, NiMo/MgO was found to be the most active one for promoting the removal of sulfur and AS. The sulfur/nitrogen/AS removal efficiencies for the NiMo/MgO catalyst increased with the treatment time, and the efficiencies at 120 min of treatment attained as high as 43%, 30%, and 70%, respectively. The MgO-supported catalysts showed excellent performance for preventing and retarding the formation of highly condensed aromatics or coke in the hydro-treatment of AS in supercritical toluene. With the presence of NiMo/MgO catalyst, hydro-treating AS in the supercritical toluene for a reaction time up to 120 min produced a strikingly low yield (<0.7%) of toluene-insoluble product.</abstract><cop>Washington, DC</cop><pub>American Chemical Society</pub><doi>10.1021/ef900126v</doi><tpages>7</tpages></addata></record> |
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subjects | Applied sciences Crude oil, natural gas and petroleum products Energy Exact sciences and technology Fossil Fuels Fuels Processing of crude oil and oils from shales and tar sands. Processes. Equipment. Refinery and treatment units |
title | Hydro-treating of Asphaltenes in Supercritical Toluene with MgO-Supported Fe, Ni, NiMo, and CoMo Catalysts |
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