Trends for mono-aromatic compounds hydrogenation over sulfided Ni, Mo and NiMo hydrotreating catalysts

The relative hydrogenation activity in typical hydrotreating conditions of toluene, m‐xylene, 1,3,5‐trimethylbenzene and 1,2,4,5‐tetramethylbenzene was unexpectedly found to decrease over a sulfided NiMo/Al2O3 catalyst and to increase over sulfided Ni/Al2O3 and Mo/Al2O3 catalysts. This change of act...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Catalysis letters 1999-01, Vol.61 (3-4), p.167-172
Hauptverfasser: QUARTARARO, J, MIGNARD, S, KASZTELAN, S
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 172
container_issue 3-4
container_start_page 167
container_title Catalysis letters
container_volume 61
creator QUARTARARO, J
MIGNARD, S
KASZTELAN, S
description The relative hydrogenation activity in typical hydrotreating conditions of toluene, m‐xylene, 1,3,5‐trimethylbenzene and 1,2,4,5‐tetramethylbenzene was unexpectedly found to decrease over a sulfided NiMo/Al2O3 catalyst and to increase over sulfided Ni/Al2O3 and Mo/Al2O3 catalysts. This change of activity trend is tentatively interpreted by the formation of a mixed NiMoS phase with a different electronic state compared to Ni or Mo sulfide phases. The nature of the aromatic compound influences strongly the magnitude of the promotion effect of Ni on the activity of the Mo in the sulfided NiMo/Al2O3 catalyst.
doi_str_mv 10.1023/a:1019093410354
format Article
fullrecord <record><control><sourceid>proquest_pasca</sourceid><recordid>TN_cdi_proquest_journals_2259022953</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2259022953</sourcerecordid><originalsourceid>FETCH-LOGICAL-c256t-88fdc03421ed1c4e13fa9910c4d039760435c44aebd2f026a920cd332f4888b23</originalsourceid><addsrcrecordid>eNotjUtLAzEUhYMoWKtrtwFdOnpzk3nEnRRfUHVTobshzaNOmUlqMiP03zvVru7HOR_nEnLJ4JYB8jt1z4BJkFww4Lk4IhOWl5hVpVwejwyMZbzE5Sk5S2kDALJkckLcIlpvEnUh0i74kKkYOtU3murQbcOw7752Joa19WMcPA0_NtI0tK4x1tD35oa-Bar8Hkf4c_toR9evqVa9anepT-fkxKk22YvDnZLPp8fF7CWbfzy_zh7mmca86LOqckYDF8isYVpYxp2SkoEWBrgsCxA810IouzLoAAslEbThHJ2oqmqFfEqu_ne3MXwPNvX1JgzRjy9rxFwCosz5aF0fLJW0al1UXjep3samU3FXM5kXEgv-CxIUZec</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2259022953</pqid></control><display><type>article</type><title>Trends for mono-aromatic compounds hydrogenation over sulfided Ni, Mo and NiMo hydrotreating catalysts</title><source>SpringerLink (Online service)</source><creator>QUARTARARO, J ; MIGNARD, S ; KASZTELAN, S</creator><creatorcontrib>QUARTARARO, J ; MIGNARD, S ; KASZTELAN, S</creatorcontrib><description>The relative hydrogenation activity in typical hydrotreating conditions of toluene, m‐xylene, 1,3,5‐trimethylbenzene and 1,2,4,5‐tetramethylbenzene was unexpectedly found to decrease over a sulfided NiMo/Al2O3 catalyst and to increase over sulfided Ni/Al2O3 and Mo/Al2O3 catalysts. This change of activity trend is tentatively interpreted by the formation of a mixed NiMoS phase with a different electronic state compared to Ni or Mo sulfide phases. The nature of the aromatic compound influences strongly the magnitude of the promotion effect of Ni on the activity of the Mo in the sulfided NiMo/Al2O3 catalyst.</description><identifier>ISSN: 1011-372X</identifier><identifier>EISSN: 1572-879X</identifier><identifier>DOI: 10.1023/a:1019093410354</identifier><language>eng</language><publisher>Dordrecht: Springer</publisher><subject>Aluminum oxide ; Aromatic compounds ; Catalysis ; Catalysts ; Catalytic reactions ; Chemistry ; Electron states ; Exact sciences and technology ; General and physical chemistry ; Hydrogenation ; Molybdenum ; Nickel ; Theory of reactions, general kinetics. Catalysis. Nomenclature, chemical documentation, computer chemistry ; Toluene ; Trimethylbenzene ; Xylene</subject><ispartof>Catalysis letters, 1999-01, Vol.61 (3-4), p.167-172</ispartof><rights>1999 INIST-CNRS</rights><rights>Catalysis Letters is a copyright of Springer, (1999). All Rights Reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c256t-88fdc03421ed1c4e13fa9910c4d039760435c44aebd2f026a920cd332f4888b23</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=1956926$$DView record in Pascal Francis$$Hfree_for_read</backlink></links><search><creatorcontrib>QUARTARARO, J</creatorcontrib><creatorcontrib>MIGNARD, S</creatorcontrib><creatorcontrib>KASZTELAN, S</creatorcontrib><title>Trends for mono-aromatic compounds hydrogenation over sulfided Ni, Mo and NiMo hydrotreating catalysts</title><title>Catalysis letters</title><description>The relative hydrogenation activity in typical hydrotreating conditions of toluene, m‐xylene, 1,3,5‐trimethylbenzene and 1,2,4,5‐tetramethylbenzene was unexpectedly found to decrease over a sulfided NiMo/Al2O3 catalyst and to increase over sulfided Ni/Al2O3 and Mo/Al2O3 catalysts. This change of activity trend is tentatively interpreted by the formation of a mixed NiMoS phase with a different electronic state compared to Ni or Mo sulfide phases. The nature of the aromatic compound influences strongly the magnitude of the promotion effect of Ni on the activity of the Mo in the sulfided NiMo/Al2O3 catalyst.</description><subject>Aluminum oxide</subject><subject>Aromatic compounds</subject><subject>Catalysis</subject><subject>Catalysts</subject><subject>Catalytic reactions</subject><subject>Chemistry</subject><subject>Electron states</subject><subject>Exact sciences and technology</subject><subject>General and physical chemistry</subject><subject>Hydrogenation</subject><subject>Molybdenum</subject><subject>Nickel</subject><subject>Theory of reactions, general kinetics. Catalysis. Nomenclature, chemical documentation, computer chemistry</subject><subject>Toluene</subject><subject>Trimethylbenzene</subject><subject>Xylene</subject><issn>1011-372X</issn><issn>1572-879X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1999</creationdate><recordtype>article</recordtype><sourceid>AFKRA</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><recordid>eNotjUtLAzEUhYMoWKtrtwFdOnpzk3nEnRRfUHVTobshzaNOmUlqMiP03zvVru7HOR_nEnLJ4JYB8jt1z4BJkFww4Lk4IhOWl5hVpVwejwyMZbzE5Sk5S2kDALJkckLcIlpvEnUh0i74kKkYOtU3murQbcOw7752Joa19WMcPA0_NtI0tK4x1tD35oa-Bar8Hkf4c_toR9evqVa9anepT-fkxKk22YvDnZLPp8fF7CWbfzy_zh7mmca86LOqckYDF8isYVpYxp2SkoEWBrgsCxA810IouzLoAAslEbThHJ2oqmqFfEqu_ne3MXwPNvX1JgzRjy9rxFwCosz5aF0fLJW0al1UXjep3samU3FXM5kXEgv-CxIUZec</recordid><startdate>19990101</startdate><enddate>19990101</enddate><creator>QUARTARARO, J</creator><creator>MIGNARD, S</creator><creator>KASZTELAN, S</creator><general>Springer</general><general>Springer Nature B.V</general><scope>IQODW</scope><scope>8FE</scope><scope>8FG</scope><scope>ABJCF</scope><scope>AFKRA</scope><scope>BENPR</scope><scope>BGLVJ</scope><scope>CCPQU</scope><scope>D1I</scope><scope>DWQXO</scope><scope>HCIFZ</scope><scope>KB.</scope><scope>PDBOC</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope></search><sort><creationdate>19990101</creationdate><title>Trends for mono-aromatic compounds hydrogenation over sulfided Ni, Mo and NiMo hydrotreating catalysts</title><author>QUARTARARO, J ; MIGNARD, S ; KASZTELAN, S</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c256t-88fdc03421ed1c4e13fa9910c4d039760435c44aebd2f026a920cd332f4888b23</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1999</creationdate><topic>Aluminum oxide</topic><topic>Aromatic compounds</topic><topic>Catalysis</topic><topic>Catalysts</topic><topic>Catalytic reactions</topic><topic>Chemistry</topic><topic>Electron states</topic><topic>Exact sciences and technology</topic><topic>General and physical chemistry</topic><topic>Hydrogenation</topic><topic>Molybdenum</topic><topic>Nickel</topic><topic>Theory of reactions, general kinetics. Catalysis. Nomenclature, chemical documentation, computer chemistry</topic><topic>Toluene</topic><topic>Trimethylbenzene</topic><topic>Xylene</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>QUARTARARO, J</creatorcontrib><creatorcontrib>MIGNARD, S</creatorcontrib><creatorcontrib>KASZTELAN, S</creatorcontrib><collection>Pascal-Francis</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Technology Collection</collection><collection>Materials Science &amp; Engineering Collection</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central</collection><collection>Technology Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Materials Science Collection</collection><collection>ProQuest Central Korea</collection><collection>SciTech Premium Collection</collection><collection>https://resources.nclive.org/materials</collection><collection>Materials science collection</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><jtitle>Catalysis letters</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>QUARTARARO, J</au><au>MIGNARD, S</au><au>KASZTELAN, S</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Trends for mono-aromatic compounds hydrogenation over sulfided Ni, Mo and NiMo hydrotreating catalysts</atitle><jtitle>Catalysis letters</jtitle><date>1999-01-01</date><risdate>1999</risdate><volume>61</volume><issue>3-4</issue><spage>167</spage><epage>172</epage><pages>167-172</pages><issn>1011-372X</issn><eissn>1572-879X</eissn><abstract>The relative hydrogenation activity in typical hydrotreating conditions of toluene, m‐xylene, 1,3,5‐trimethylbenzene and 1,2,4,5‐tetramethylbenzene was unexpectedly found to decrease over a sulfided NiMo/Al2O3 catalyst and to increase over sulfided Ni/Al2O3 and Mo/Al2O3 catalysts. This change of activity trend is tentatively interpreted by the formation of a mixed NiMoS phase with a different electronic state compared to Ni or Mo sulfide phases. The nature of the aromatic compound influences strongly the magnitude of the promotion effect of Ni on the activity of the Mo in the sulfided NiMo/Al2O3 catalyst.</abstract><cop>Dordrecht</cop><pub>Springer</pub><doi>10.1023/a:1019093410354</doi><tpages>6</tpages></addata></record>
fulltext fulltext
identifier ISSN: 1011-372X
ispartof Catalysis letters, 1999-01, Vol.61 (3-4), p.167-172
issn 1011-372X
1572-879X
language eng
recordid cdi_proquest_journals_2259022953
source SpringerLink (Online service)
subjects Aluminum oxide
Aromatic compounds
Catalysis
Catalysts
Catalytic reactions
Chemistry
Electron states
Exact sciences and technology
General and physical chemistry
Hydrogenation
Molybdenum
Nickel
Theory of reactions, general kinetics. Catalysis. Nomenclature, chemical documentation, computer chemistry
Toluene
Trimethylbenzene
Xylene
title Trends for mono-aromatic compounds hydrogenation over sulfided Ni, Mo and NiMo hydrotreating catalysts
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-28T07%3A35%3A56IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_pasca&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Trends%20for%20mono-aromatic%20compounds%20hydrogenation%20over%20sulfided%20Ni,%20Mo%20and%20NiMo%20hydrotreating%20catalysts&rft.jtitle=Catalysis%20letters&rft.au=QUARTARARO,%20J&rft.date=1999-01-01&rft.volume=61&rft.issue=3-4&rft.spage=167&rft.epage=172&rft.pages=167-172&rft.issn=1011-372X&rft.eissn=1572-879X&rft_id=info:doi/10.1023/a:1019093410354&rft_dat=%3Cproquest_pasca%3E2259022953%3C/proquest_pasca%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=2259022953&rft_id=info:pmid/&rfr_iscdi=true