Structure of Mn–Zr mixed oxides catalysts and their catalytic performance in the gas-phase oxidation of chlorocarbons
The catalytic activity and selectivity of manganese zirconia mixed oxides were evaluated for the oxidation of two common chlorinated pollutants found in waste streams, namely 1,2-dichloroethane (DCE) and trichloroethylene (TCE). Mixed oxides with varying Mn–Zr content were prepared by coprecipitatio...
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creator | Gutiérrez-Ortiz, Jose I. de Rivas, Beatriz López-Fonseca, Rubén Martín, Susana González-Velasco, Juan R. |
description | The catalytic activity and selectivity of manganese zirconia mixed oxides were evaluated for the oxidation of two common chlorinated pollutants found in waste streams, namely 1,2-dichloroethane (DCE) and trichloroethylene (TCE). Mixed oxides with varying Mn–Zr content were prepared by coprecipitation via nitrates, and subsequent calcination at 600
°C for 4
h in air. These catalysts were characterised by means of several techniques such as atomic emission spectrometry, N
2 adsorption–desorption, powder X-ray diffraction, temperature-programmed desorption of ammonia, pyridine adsorption followed by diffuse reflectance infrared spectroscopy and temperature-programmed reduction with hydrogen.
The active catalytic behaviour of Mn–Zr mixed oxides was ascribed to a substantial surface acidity combined with readily accessible active oxygen species. Hence, the mixed oxide with 40
mol% manganese content was found to be an optimum catalyst for the combustion of both chlorocarbons with a
T
50 value around 305 and 315
°C for DCE and TCE oxidation, respectively. The major oxidation products were carbon dioxide, hydrogen chloride and chlorine. It was observed that the formation of both CO
2 and Cl
2 was promoted with Mn loading. |
doi_str_mv | 10.1016/j.chemosphere.2007.02.025 |
format | Article |
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°C for 4
h in air. These catalysts were characterised by means of several techniques such as atomic emission spectrometry, N
2 adsorption–desorption, powder X-ray diffraction, temperature-programmed desorption of ammonia, pyridine adsorption followed by diffuse reflectance infrared spectroscopy and temperature-programmed reduction with hydrogen.
The active catalytic behaviour of Mn–Zr mixed oxides was ascribed to a substantial surface acidity combined with readily accessible active oxygen species. Hence, the mixed oxide with 40
mol% manganese content was found to be an optimum catalyst for the combustion of both chlorocarbons with a
T
50 value around 305 and 315
°C for DCE and TCE oxidation, respectively. The major oxidation products were carbon dioxide, hydrogen chloride and chlorine. It was observed that the formation of both CO
2 and Cl
2 was promoted with Mn loading.</description><identifier>ISSN: 0045-6535</identifier><identifier>EISSN: 1879-1298</identifier><identifier>DOI: 10.1016/j.chemosphere.2007.02.025</identifier><identifier>PMID: 17395240</identifier><identifier>CODEN: CMSHAF</identifier><language>eng</language><publisher>Oxford: Elsevier Ltd</publisher><subject>1,2-Dichloroethane ; Applied sciences ; Atmospheric pollution ; Catalysis ; Catalysts: preparations and properties ; Catalytic oxidation ; Chemistry ; Chlorinated VOC ; Ethylene Dichlorides - chemistry ; Exact sciences and technology ; Gases - chemistry ; General and physical chemistry ; General processes of purification and dust removal ; Manganese - chemistry ; Manganese–zirconium mixed oxides ; Oxides - chemistry ; Pollution ; Prevention and purification methods ; Theory of reactions, general kinetics. Catalysis. Nomenclature, chemical documentation, computer chemistry ; Trichloroethylene ; Trichloroethylene - chemistry ; Zirconium - chemistry</subject><ispartof>Chemosphere (Oxford), 2007-06, Vol.68 (6), p.1004-1012</ispartof><rights>2007 Elsevier Ltd</rights><rights>2007 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c467t-fcf925119b84904f7729242eaf84fe018588f2f54d5084cfc36664fc9394ccbc3</citedby><cites>FETCH-LOGICAL-c467t-fcf925119b84904f7729242eaf84fe018588f2f54d5084cfc36664fc9394ccbc3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.chemosphere.2007.02.025$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3550,27924,27925,45995</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=18791312$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/17395240$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Gutiérrez-Ortiz, Jose I.</creatorcontrib><creatorcontrib>de Rivas, Beatriz</creatorcontrib><creatorcontrib>López-Fonseca, Rubén</creatorcontrib><creatorcontrib>Martín, Susana</creatorcontrib><creatorcontrib>González-Velasco, Juan R.</creatorcontrib><title>Structure of Mn–Zr mixed oxides catalysts and their catalytic performance in the gas-phase oxidation of chlorocarbons</title><title>Chemosphere (Oxford)</title><addtitle>Chemosphere</addtitle><description>The catalytic activity and selectivity of manganese zirconia mixed oxides were evaluated for the oxidation of two common chlorinated pollutants found in waste streams, namely 1,2-dichloroethane (DCE) and trichloroethylene (TCE). Mixed oxides with varying Mn–Zr content were prepared by coprecipitation via nitrates, and subsequent calcination at 600
°C for 4
h in air. These catalysts were characterised by means of several techniques such as atomic emission spectrometry, N
2 adsorption–desorption, powder X-ray diffraction, temperature-programmed desorption of ammonia, pyridine adsorption followed by diffuse reflectance infrared spectroscopy and temperature-programmed reduction with hydrogen.
The active catalytic behaviour of Mn–Zr mixed oxides was ascribed to a substantial surface acidity combined with readily accessible active oxygen species. Hence, the mixed oxide with 40
mol% manganese content was found to be an optimum catalyst for the combustion of both chlorocarbons with a
T
50 value around 305 and 315
°C for DCE and TCE oxidation, respectively. The major oxidation products were carbon dioxide, hydrogen chloride and chlorine. It was observed that the formation of both CO
2 and Cl
2 was promoted with Mn loading.</description><subject>1,2-Dichloroethane</subject><subject>Applied sciences</subject><subject>Atmospheric pollution</subject><subject>Catalysis</subject><subject>Catalysts: preparations and properties</subject><subject>Catalytic oxidation</subject><subject>Chemistry</subject><subject>Chlorinated VOC</subject><subject>Ethylene Dichlorides - chemistry</subject><subject>Exact sciences and technology</subject><subject>Gases - chemistry</subject><subject>General and physical chemistry</subject><subject>General processes of purification and dust removal</subject><subject>Manganese - chemistry</subject><subject>Manganese–zirconium mixed oxides</subject><subject>Oxides - chemistry</subject><subject>Pollution</subject><subject>Prevention and purification methods</subject><subject>Theory of reactions, general kinetics. Catalysis. Nomenclature, chemical documentation, computer chemistry</subject><subject>Trichloroethylene</subject><subject>Trichloroethylene - chemistry</subject><subject>Zirconium - chemistry</subject><issn>0045-6535</issn><issn>1879-1298</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2007</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNksFu1DAQhiMEokvhFZA5wC3L2LGT-IhWUJCKOAAXLpbXGROvkjjY3tLe-g68IU-Cw0YqtyKNZMn-5h_Ln4viBYUtBVq_PmxNj6OPc48Btwyg2QLLJR4UG9o2sqRMtg-LDQAXZS0qcVY8ifEAkJuFfFyc0aaSgnHYFD8_p3A06RiQeEs-Tr9vf30LZHTX2BF_7TqMxOikh5uYItFTR1KPLqx7yRkyY7A-jHoySNy0HJPvOpZzryP-TdDJ-WkJN_3ggzc67P0UnxaPrB4iPlvX8-Lru7dfdu_Ly08XH3ZvLkvD6yaV1ljJBKVy33IJ3DYNk4wz1LblFoG2om0ts4J3AlpurKnquubWyEpyY_amOi9enXLn4H8cMSY1umhwGPSE_hhVA7yqAap7QQY1h5qJe0HKWxCNgAzKE2iCjzGgVXNwow43ioJaPKqD-sejWjwqYLmWIc_XIcf9iN1d5youAy9XQEejBxuyABfvuPwLaEVZ5nYnDvMjXzkMKhqHWVbnApqkOu_-4zp_ALJvxA8</recordid><startdate>20070601</startdate><enddate>20070601</enddate><creator>Gutiérrez-Ortiz, Jose I.</creator><creator>de Rivas, Beatriz</creator><creator>López-Fonseca, Rubén</creator><creator>Martín, Susana</creator><creator>González-Velasco, Juan R.</creator><general>Elsevier Ltd</general><general>Elsevier</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7ST</scope><scope>C1K</scope><scope>SOI</scope><scope>7QH</scope><scope>7TV</scope><scope>7UA</scope><scope>7X8</scope></search><sort><creationdate>20070601</creationdate><title>Structure of Mn–Zr mixed oxides catalysts and their catalytic performance in the gas-phase oxidation of chlorocarbons</title><author>Gutiérrez-Ortiz, Jose I. ; de Rivas, Beatriz ; López-Fonseca, Rubén ; Martín, Susana ; González-Velasco, Juan R.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c467t-fcf925119b84904f7729242eaf84fe018588f2f54d5084cfc36664fc9394ccbc3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2007</creationdate><topic>1,2-Dichloroethane</topic><topic>Applied sciences</topic><topic>Atmospheric pollution</topic><topic>Catalysis</topic><topic>Catalysts: preparations and properties</topic><topic>Catalytic oxidation</topic><topic>Chemistry</topic><topic>Chlorinated VOC</topic><topic>Ethylene Dichlorides - chemistry</topic><topic>Exact sciences and technology</topic><topic>Gases - chemistry</topic><topic>General and physical chemistry</topic><topic>General processes of purification and dust removal</topic><topic>Manganese - chemistry</topic><topic>Manganese–zirconium mixed oxides</topic><topic>Oxides - chemistry</topic><topic>Pollution</topic><topic>Prevention and purification methods</topic><topic>Theory of reactions, general kinetics. Catalysis. Nomenclature, chemical documentation, computer chemistry</topic><topic>Trichloroethylene</topic><topic>Trichloroethylene - chemistry</topic><topic>Zirconium - chemistry</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Gutiérrez-Ortiz, Jose I.</creatorcontrib><creatorcontrib>de Rivas, Beatriz</creatorcontrib><creatorcontrib>López-Fonseca, Rubén</creatorcontrib><creatorcontrib>Martín, Susana</creatorcontrib><creatorcontrib>González-Velasco, Juan R.</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Environment Abstracts</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Environment Abstracts</collection><collection>Aqualine</collection><collection>Pollution Abstracts</collection><collection>Water Resources Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Chemosphere (Oxford)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Gutiérrez-Ortiz, Jose I.</au><au>de Rivas, Beatriz</au><au>López-Fonseca, Rubén</au><au>Martín, Susana</au><au>González-Velasco, Juan R.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Structure of Mn–Zr mixed oxides catalysts and their catalytic performance in the gas-phase oxidation of chlorocarbons</atitle><jtitle>Chemosphere (Oxford)</jtitle><addtitle>Chemosphere</addtitle><date>2007-06-01</date><risdate>2007</risdate><volume>68</volume><issue>6</issue><spage>1004</spage><epage>1012</epage><pages>1004-1012</pages><issn>0045-6535</issn><eissn>1879-1298</eissn><coden>CMSHAF</coden><abstract>The catalytic activity and selectivity of manganese zirconia mixed oxides were evaluated for the oxidation of two common chlorinated pollutants found in waste streams, namely 1,2-dichloroethane (DCE) and trichloroethylene (TCE). Mixed oxides with varying Mn–Zr content were prepared by coprecipitation via nitrates, and subsequent calcination at 600
°C for 4
h in air. These catalysts were characterised by means of several techniques such as atomic emission spectrometry, N
2 adsorption–desorption, powder X-ray diffraction, temperature-programmed desorption of ammonia, pyridine adsorption followed by diffuse reflectance infrared spectroscopy and temperature-programmed reduction with hydrogen.
The active catalytic behaviour of Mn–Zr mixed oxides was ascribed to a substantial surface acidity combined with readily accessible active oxygen species. Hence, the mixed oxide with 40
mol% manganese content was found to be an optimum catalyst for the combustion of both chlorocarbons with a
T
50 value around 305 and 315
°C for DCE and TCE oxidation, respectively. The major oxidation products were carbon dioxide, hydrogen chloride and chlorine. It was observed that the formation of both CO
2 and Cl
2 was promoted with Mn loading.</abstract><cop>Oxford</cop><pub>Elsevier Ltd</pub><pmid>17395240</pmid><doi>10.1016/j.chemosphere.2007.02.025</doi><tpages>9</tpages></addata></record> |
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subjects | 1,2-Dichloroethane Applied sciences Atmospheric pollution Catalysis Catalysts: preparations and properties Catalytic oxidation Chemistry Chlorinated VOC Ethylene Dichlorides - chemistry Exact sciences and technology Gases - chemistry General and physical chemistry General processes of purification and dust removal Manganese - chemistry Manganese–zirconium mixed oxides Oxides - chemistry Pollution Prevention and purification methods Theory of reactions, general kinetics. Catalysis. Nomenclature, chemical documentation, computer chemistry Trichloroethylene Trichloroethylene - chemistry Zirconium - chemistry |
title | Structure of Mn–Zr mixed oxides catalysts and their catalytic performance in the gas-phase oxidation of chlorocarbons |
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