Hydrodechlorination of Carbon Tetrachloride over Pt/MgO
Hydrodechlorination of carbon tetrachloride (CCl4) has been studied at various reaction temperatures, mole ratios (H2/CCl4), and WHSVs over 1% Pt/MgO. The main factors determining conversion of CCl4and deactivation of the catalyst were reaction temperature and H2/CCl4mole ratio. The optimum reaction...
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| Veröffentlicht in: | Journal of Catalysis 1996-07, Vol.161 (2), p.790-797 |
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| container_issue | 2 |
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| container_title | Journal of Catalysis |
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| creator | Chul Choi, Hyun Choi, Sun Hee Yang, O Bong Lee, Jae Sung Lee, Kyung Hee Kim, Young Gul |
| description | Hydrodechlorination of carbon tetrachloride (CCl4) has been studied at various reaction temperatures, mole ratios (H2/CCl4), and WHSVs over 1% Pt/MgO. The main factors determining conversion of CCl4and deactivation of the catalyst were reaction temperature and H2/CCl4mole ratio. The optimum reaction conditions for obtaining stable and high conversions of CCl4above 90% were the reaction temperature of 413 K, H2/CCl4mole ratio of 9, and WHSV of 9000 liters/kg/h. The surface area of catalyst decreased due to phase change of MgO to MgCl2·xH2O during reaction. Relative to fresh catalyst, the amounts of carbon and chlorine increased and that of oxygen decreased in used catalyst, especially in deactivated catalyst. The catalyst used for the steady-state reaction did not chemisorb H2at room temperature, but chemisorbed nearly the same amounts of H2as those observed for the fresh catalyst at 373 K. From the XPS and XAFS measurements the active phase of Pt during hydrodechlorination appeared to be a surface Pt(II) species with Cl ligands, while the bulk remained as Pt metal. |
| doi_str_mv | 10.1006/jcat.1996.0242 |
| format | Article |
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The main factors determining conversion of CCl4and deactivation of the catalyst were reaction temperature and H2/CCl4mole ratio. The optimum reaction conditions for obtaining stable and high conversions of CCl4above 90% were the reaction temperature of 413 K, H2/CCl4mole ratio of 9, and WHSV of 9000 liters/kg/h. The surface area of catalyst decreased due to phase change of MgO to MgCl2·xH2O during reaction. Relative to fresh catalyst, the amounts of carbon and chlorine increased and that of oxygen decreased in used catalyst, especially in deactivated catalyst. The catalyst used for the steady-state reaction did not chemisorb H2at room temperature, but chemisorbed nearly the same amounts of H2as those observed for the fresh catalyst at 373 K. From the XPS and XAFS measurements the active phase of Pt during hydrodechlorination appeared to be a surface Pt(II) species with Cl ligands, while the bulk remained as Pt metal.</description><identifier>ISSN: 0021-9517</identifier><identifier>EISSN: 1090-2694</identifier><identifier>DOI: 10.1006/jcat.1996.0242</identifier><identifier>CODEN: JCTLA5</identifier><language>eng</language><publisher>Amsterdam: Elsevier Inc</publisher><subject>40 CHEMISTRY ; CARBON TETRACHLORIDE ; Catalysis ; CATALYST SUPPORTS ; CATALYSTS ; CATALYTIC EFFECTS ; Catalytic reactions ; Chemistry ; DECHLORINATION ; Exact sciences and technology ; General and physical chemistry ; HYDROGENATION ; MAGNESIUM OXIDES ; PHOTOELECTRON SPECTROSCOPY ; PLATINUM ; Theory of reactions, general kinetics. Catalysis. Nomenclature, chemical documentation, computer chemistry</subject><ispartof>Journal of Catalysis, 1996-07, Vol.161 (2), p.790-797</ispartof><rights>1996 Academic Press</rights><rights>1996 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c341t-98e6ab98a3ec5d6ea5b68e800320e1c7d68bee46fe7444444c90160bf2dcf8823</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0021951796902420$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,881,3537,27901,27902,65306</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=3183923$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.osti.gov/biblio/447123$$D View this record in Osti.gov$$Hfree_for_read</backlink></links><search><creatorcontrib>Chul Choi, Hyun</creatorcontrib><creatorcontrib>Choi, Sun Hee</creatorcontrib><creatorcontrib>Yang, O Bong</creatorcontrib><creatorcontrib>Lee, Jae Sung</creatorcontrib><creatorcontrib>Lee, Kyung Hee</creatorcontrib><creatorcontrib>Kim, Young Gul</creatorcontrib><title>Hydrodechlorination of Carbon Tetrachloride over Pt/MgO</title><title>Journal of Catalysis</title><description>Hydrodechlorination of carbon tetrachloride (CCl4) has been studied at various reaction temperatures, mole ratios (H2/CCl4), and WHSVs over 1% Pt/MgO. The main factors determining conversion of CCl4and deactivation of the catalyst were reaction temperature and H2/CCl4mole ratio. The optimum reaction conditions for obtaining stable and high conversions of CCl4above 90% were the reaction temperature of 413 K, H2/CCl4mole ratio of 9, and WHSV of 9000 liters/kg/h. The surface area of catalyst decreased due to phase change of MgO to MgCl2·xH2O during reaction. Relative to fresh catalyst, the amounts of carbon and chlorine increased and that of oxygen decreased in used catalyst, especially in deactivated catalyst. The catalyst used for the steady-state reaction did not chemisorb H2at room temperature, but chemisorbed nearly the same amounts of H2as those observed for the fresh catalyst at 373 K. From the XPS and XAFS measurements the active phase of Pt during hydrodechlorination appeared to be a surface Pt(II) species with Cl ligands, while the bulk remained as Pt metal.</description><subject>40 CHEMISTRY</subject><subject>CARBON TETRACHLORIDE</subject><subject>Catalysis</subject><subject>CATALYST SUPPORTS</subject><subject>CATALYSTS</subject><subject>CATALYTIC EFFECTS</subject><subject>Catalytic reactions</subject><subject>Chemistry</subject><subject>DECHLORINATION</subject><subject>Exact sciences and technology</subject><subject>General and physical chemistry</subject><subject>HYDROGENATION</subject><subject>MAGNESIUM OXIDES</subject><subject>PHOTOELECTRON SPECTROSCOPY</subject><subject>PLATINUM</subject><subject>Theory of reactions, general kinetics. Catalysis. Nomenclature, chemical documentation, computer chemistry</subject><issn>0021-9517</issn><issn>1090-2694</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1996</creationdate><recordtype>article</recordtype><recordid>eNp1UD1PwzAQtRBIlMLKHCTWhLOTOPaIKqBIRWUos-XYF3BV4sq2KvXfkzSIjVvupHsfd4-QWwoFBeAPW6NTQaXkBbCKnZEZBQk547I6JzMARnNZ0-aSXMW4BaC0rsWMNMujDd6i-dr54HqdnO8z32ULHdph2mAKetpZzPwBQ_aeHt4-19fkotO7iDe_fU4-np82i2W-Wr-8Lh5XuSkrmnIpkOtWCl2iqS1HXbdcoAAoGSA1jeWiRax4h011KiOBcmg7Zk0nBCvn5G7S9TE5FY1Lw6nG9z2apKqqoawcMMWEMcHHGLBT--C-dTgqCmqMRo3RqDEaNUYzEO4nwl5Ho3dd0L1x8Y9VUlHKk66YYDg8eHAYRn_sDVoXRnvr3X8OP1IodoI</recordid><startdate>19960701</startdate><enddate>19960701</enddate><creator>Chul Choi, Hyun</creator><creator>Choi, Sun Hee</creator><creator>Yang, O Bong</creator><creator>Lee, Jae Sung</creator><creator>Lee, Kyung Hee</creator><creator>Kim, Young Gul</creator><general>Elsevier Inc</general><general>Elsevier</general><scope>IQODW</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>OTOTI</scope></search><sort><creationdate>19960701</creationdate><title>Hydrodechlorination of Carbon Tetrachloride over Pt/MgO</title><author>Chul Choi, Hyun ; Choi, Sun Hee ; Yang, O Bong ; Lee, Jae Sung ; Lee, Kyung Hee ; Kim, Young Gul</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c341t-98e6ab98a3ec5d6ea5b68e800320e1c7d68bee46fe7444444c90160bf2dcf8823</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1996</creationdate><topic>40 CHEMISTRY</topic><topic>CARBON TETRACHLORIDE</topic><topic>Catalysis</topic><topic>CATALYST SUPPORTS</topic><topic>CATALYSTS</topic><topic>CATALYTIC EFFECTS</topic><topic>Catalytic reactions</topic><topic>Chemistry</topic><topic>DECHLORINATION</topic><topic>Exact sciences and technology</topic><topic>General and physical chemistry</topic><topic>HYDROGENATION</topic><topic>MAGNESIUM OXIDES</topic><topic>PHOTOELECTRON SPECTROSCOPY</topic><topic>PLATINUM</topic><topic>Theory of reactions, general kinetics. Catalysis. Nomenclature, chemical documentation, computer chemistry</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Chul Choi, Hyun</creatorcontrib><creatorcontrib>Choi, Sun Hee</creatorcontrib><creatorcontrib>Yang, O Bong</creatorcontrib><creatorcontrib>Lee, Jae Sung</creatorcontrib><creatorcontrib>Lee, Kyung Hee</creatorcontrib><creatorcontrib>Kim, Young Gul</creatorcontrib><collection>Pascal-Francis</collection><collection>CrossRef</collection><collection>OSTI.GOV</collection><jtitle>Journal of Catalysis</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Chul Choi, Hyun</au><au>Choi, Sun Hee</au><au>Yang, O Bong</au><au>Lee, Jae Sung</au><au>Lee, Kyung Hee</au><au>Kim, Young Gul</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Hydrodechlorination of Carbon Tetrachloride over Pt/MgO</atitle><jtitle>Journal of Catalysis</jtitle><date>1996-07-01</date><risdate>1996</risdate><volume>161</volume><issue>2</issue><spage>790</spage><epage>797</epage><pages>790-797</pages><issn>0021-9517</issn><eissn>1090-2694</eissn><coden>JCTLA5</coden><abstract>Hydrodechlorination of carbon tetrachloride (CCl4) has been studied at various reaction temperatures, mole ratios (H2/CCl4), and WHSVs over 1% Pt/MgO. The main factors determining conversion of CCl4and deactivation of the catalyst were reaction temperature and H2/CCl4mole ratio. The optimum reaction conditions for obtaining stable and high conversions of CCl4above 90% were the reaction temperature of 413 K, H2/CCl4mole ratio of 9, and WHSV of 9000 liters/kg/h. The surface area of catalyst decreased due to phase change of MgO to MgCl2·xH2O during reaction. Relative to fresh catalyst, the amounts of carbon and chlorine increased and that of oxygen decreased in used catalyst, especially in deactivated catalyst. The catalyst used for the steady-state reaction did not chemisorb H2at room temperature, but chemisorbed nearly the same amounts of H2as those observed for the fresh catalyst at 373 K. From the XPS and XAFS measurements the active phase of Pt during hydrodechlorination appeared to be a surface Pt(II) species with Cl ligands, while the bulk remained as Pt metal.</abstract><cop>Amsterdam</cop><pub>Elsevier Inc</pub><doi>10.1006/jcat.1996.0242</doi><tpages>8</tpages></addata></record> |
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| subjects | 40 CHEMISTRY CARBON TETRACHLORIDE Catalysis CATALYST SUPPORTS CATALYSTS CATALYTIC EFFECTS Catalytic reactions Chemistry DECHLORINATION Exact sciences and technology General and physical chemistry HYDROGENATION MAGNESIUM OXIDES PHOTOELECTRON SPECTROSCOPY PLATINUM Theory of reactions, general kinetics. Catalysis. Nomenclature, chemical documentation, computer chemistry |
| title | Hydrodechlorination of Carbon Tetrachloride over Pt/MgO |
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