Selective oxidative dehydrogenation of ethane over SnO2-promoted NiO catalysts
Sn-doped NiO catalysts are highly efficient for the oxidative dehydrogenation of ethane. Addition of a tiny amount of tin highly increases selectivity to ethylene. [Display omitted] ► NiSnO mixed oxides catalysts for ethane ODH were prepared and investigated. ► Addition of a tiny amount of tin highl...
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| Veröffentlicht in: | Journal of catalysis 2012-11, Vol.295, p.104-114 |
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| creator | Solsona, B. Concepción, P. Demicol, B. Hernández, S. Delgado, J.J. Calvino, J.J. López Nieto, J.M. |
| description | Sn-doped NiO catalysts are highly efficient for the oxidative dehydrogenation of ethane. Addition of a tiny amount of tin highly increases selectivity to ethylene. [Display omitted]
► NiSnO mixed oxides catalysts for ethane ODH were prepared and investigated. ► Addition of a tiny amount of tin highly increases selectivity to ethylene. ► Changes in the nature of Ni species on the surface of catalysts are observed. ► Changes in the crystal size of NiO particles with Sn-loading are observed.
NiSnO mixed oxides catalysts have been investigated for the oxidative dehydrogenation of ethane. The catalysts were prepared through the evaporation of aqueous solutions of nickel nitrate and tin oxalate and finally calcined in air at 500°C for 2h. These materials have been characterized by several techniques (N2-adsorption, X-ray diffraction, High-Resolution Electron Microscopy, temperature programmed reduction, X-Ray Photoelectron Spectroscopy, Fourier Transformed Infrared Spectroscopy of adsorbed CO and 18O/16O isotope exchange). The addition of just a tiny amount of tin highly increases the selectivity to ethylene (from ca. 40% to 80–90%). Thus, high selectivity to ethylene (near to 90%) is observed on samples with high Ni/Sn atomic ratios (3 |
| doi_str_mv | 10.1016/j.jcat.2012.07.028 |
| format | Article |
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► NiSnO mixed oxides catalysts for ethane ODH were prepared and investigated. ► Addition of a tiny amount of tin highly increases selectivity to ethylene. ► Changes in the nature of Ni species on the surface of catalysts are observed. ► Changes in the crystal size of NiO particles with Sn-loading are observed.
NiSnO mixed oxides catalysts have been investigated for the oxidative dehydrogenation of ethane. The catalysts were prepared through the evaporation of aqueous solutions of nickel nitrate and tin oxalate and finally calcined in air at 500°C for 2h. These materials have been characterized by several techniques (N2-adsorption, X-ray diffraction, High-Resolution Electron Microscopy, temperature programmed reduction, X-Ray Photoelectron Spectroscopy, Fourier Transformed Infrared Spectroscopy of adsorbed CO and 18O/16O isotope exchange). The addition of just a tiny amount of tin highly increases the selectivity to ethylene (from ca. 40% to 80–90%). Thus, high selectivity to ethylene (near to 90%) is observed on samples with high Ni/Sn atomic ratios (3<Ni/Sn<50), in which no influence of ethane conversion on selectivity to ethylene is observed (suggesting high stability of ethylene on these catalysts). Additionally, for low Sn-loadings, an increase in the catalytic activity has also been observed. The enhanced catalytic properties have been explained in terms of changes in the nature of Ni species on the catalyst surface, which can be considered as the active sites. The nature of Ni species is related to changes in the crystal size of NiO particles (and surface area) of catalysts as well as to the presence of SnOx crystals. In addition, the role of the presence of acid sites on the catalyst surface on the selectivity to ethylene is also discussed.</description><identifier>ISSN: 0021-9517</identifier><identifier>EISSN: 1090-2694</identifier><identifier>DOI: 10.1016/j.jcat.2012.07.028</identifier><identifier>CODEN: JCTLA5</identifier><language>eng</language><publisher>Amsterdam: Elsevier Inc</publisher><subject>active sites ; air ; aqueous solutions ; Catalysis ; Catalyst characterization (XPS, HREM, oxygen isotope exchange, FTIR CO adsorbed) ; Catalysts ; catalytic activity ; Catalytic oxidation ; Chemical reactions ; Chemistry ; crystals ; dehydrogenation ; electron microscopy ; ethane ; Ethane ODH ; Ethane oxidation ; Ethylene ; evaporation ; Exact sciences and technology ; General and physical chemistry ; infrared spectroscopy ; isotopes ; nickel ; Nickel oxide ; nitrates ; oxides ; surface area ; Surface physical chemistry ; temperature ; Theory of reactions, general kinetics. Catalysis. Nomenclature, chemical documentation, computer chemistry ; tin ; Tin oxide ; X-ray diffraction ; X-ray photoelectron spectroscopy</subject><ispartof>Journal of catalysis, 2012-11, Vol.295, p.104-114</ispartof><rights>2012 Elsevier Inc.</rights><rights>2015 INIST-CNRS</rights><rights>Copyright © 2012 Elsevier B.V. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c349t-6253b1874b43bef2e4f6a3dbd006a387fde1b6f6365de70057dfb184c7c886043</citedby><cites>FETCH-LOGICAL-c349t-6253b1874b43bef2e4f6a3dbd006a387fde1b6f6365de70057dfb184c7c886043</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0021951712002333$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3537,27901,27902,65306</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=26564766$$DView record in Pascal Francis$$Hfree_for_read</backlink></links><search><creatorcontrib>Solsona, B.</creatorcontrib><creatorcontrib>Concepción, P.</creatorcontrib><creatorcontrib>Demicol, B.</creatorcontrib><creatorcontrib>Hernández, S.</creatorcontrib><creatorcontrib>Delgado, J.J.</creatorcontrib><creatorcontrib>Calvino, J.J.</creatorcontrib><creatorcontrib>López Nieto, J.M.</creatorcontrib><title>Selective oxidative dehydrogenation of ethane over SnO2-promoted NiO catalysts</title><title>Journal of catalysis</title><description>Sn-doped NiO catalysts are highly efficient for the oxidative dehydrogenation of ethane. Addition of a tiny amount of tin highly increases selectivity to ethylene. [Display omitted]
► NiSnO mixed oxides catalysts for ethane ODH were prepared and investigated. ► Addition of a tiny amount of tin highly increases selectivity to ethylene. ► Changes in the nature of Ni species on the surface of catalysts are observed. ► Changes in the crystal size of NiO particles with Sn-loading are observed.
NiSnO mixed oxides catalysts have been investigated for the oxidative dehydrogenation of ethane. The catalysts were prepared through the evaporation of aqueous solutions of nickel nitrate and tin oxalate and finally calcined in air at 500°C for 2h. These materials have been characterized by several techniques (N2-adsorption, X-ray diffraction, High-Resolution Electron Microscopy, temperature programmed reduction, X-Ray Photoelectron Spectroscopy, Fourier Transformed Infrared Spectroscopy of adsorbed CO and 18O/16O isotope exchange). The addition of just a tiny amount of tin highly increases the selectivity to ethylene (from ca. 40% to 80–90%). Thus, high selectivity to ethylene (near to 90%) is observed on samples with high Ni/Sn atomic ratios (3<Ni/Sn<50), in which no influence of ethane conversion on selectivity to ethylene is observed (suggesting high stability of ethylene on these catalysts). Additionally, for low Sn-loadings, an increase in the catalytic activity has also been observed. The enhanced catalytic properties have been explained in terms of changes in the nature of Ni species on the catalyst surface, which can be considered as the active sites. The nature of Ni species is related to changes in the crystal size of NiO particles (and surface area) of catalysts as well as to the presence of SnOx crystals. In addition, the role of the presence of acid sites on the catalyst surface on the selectivity to ethylene is also discussed.</description><subject>active sites</subject><subject>air</subject><subject>aqueous solutions</subject><subject>Catalysis</subject><subject>Catalyst characterization (XPS, HREM, oxygen isotope exchange, FTIR CO adsorbed)</subject><subject>Catalysts</subject><subject>catalytic activity</subject><subject>Catalytic oxidation</subject><subject>Chemical reactions</subject><subject>Chemistry</subject><subject>crystals</subject><subject>dehydrogenation</subject><subject>electron microscopy</subject><subject>ethane</subject><subject>Ethane ODH</subject><subject>Ethane oxidation</subject><subject>Ethylene</subject><subject>evaporation</subject><subject>Exact sciences and technology</subject><subject>General and physical chemistry</subject><subject>infrared spectroscopy</subject><subject>isotopes</subject><subject>nickel</subject><subject>Nickel oxide</subject><subject>nitrates</subject><subject>oxides</subject><subject>surface area</subject><subject>Surface physical chemistry</subject><subject>temperature</subject><subject>Theory of reactions, general kinetics. Catalysis. Nomenclature, chemical documentation, computer chemistry</subject><subject>tin</subject><subject>Tin oxide</subject><subject>X-ray diffraction</subject><subject>X-ray photoelectron spectroscopy</subject><issn>0021-9517</issn><issn>1090-2694</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2012</creationdate><recordtype>article</recordtype><recordid>eNp9kE1r3DAQhkVJoJuPP9BLDaFHOzOSLXkhlxD6BSF72OQsZGmUyGysRHKW7r-vtht6zGlm4Jl3hoexLwgNAsrLsRmtmRsOyBtQDfD-E1sgLKHmctkesQUAx3rZofrMTnIeARC7rl-wuzVtyM5hS1X8E5z51zl62rkUH2kqc5yq6Cuan8xUmC2laj2teP2S4nOcyVV3YVWV22azy3M-Y8febDKdv9dT9vDj-_3Nr_p29fP3zfVtbUW7nGvJOzFgr9qhFQN5Tq2XRrjBAZTaK-8IB-mlkJ0jBdAp5wvfWmX7XkIrTtnFIbe88fpGedZjfEtTOakRUXApUIhC8QNlU8w5kdcvKTybtNMIeu9Nj3rvTe-9aVC6eCtL396jTbZm45OZbMj_N7nsZKukLNzXA-dN1OYxFeZhXYIkFLkd4p64OhBUTGwDJZ1toMmSC6k41y6Gjx75C_h9jC8</recordid><startdate>20121101</startdate><enddate>20121101</enddate><creator>Solsona, B.</creator><creator>Concepción, P.</creator><creator>Demicol, B.</creator><creator>Hernández, S.</creator><creator>Delgado, J.J.</creator><creator>Calvino, J.J.</creator><creator>López Nieto, J.M.</creator><general>Elsevier Inc</general><general>Elsevier</general><general>Elsevier BV</general><scope>FBQ</scope><scope>IQODW</scope><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>20121101</creationdate><title>Selective oxidative dehydrogenation of ethane over SnO2-promoted NiO catalysts</title><author>Solsona, B. ; Concepción, P. ; Demicol, B. ; Hernández, S. ; Delgado, J.J. ; Calvino, J.J. ; López Nieto, J.M.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c349t-6253b1874b43bef2e4f6a3dbd006a387fde1b6f6365de70057dfb184c7c886043</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2012</creationdate><topic>active sites</topic><topic>air</topic><topic>aqueous solutions</topic><topic>Catalysis</topic><topic>Catalyst characterization (XPS, HREM, oxygen isotope exchange, FTIR CO adsorbed)</topic><topic>Catalysts</topic><topic>catalytic activity</topic><topic>Catalytic oxidation</topic><topic>Chemical reactions</topic><topic>Chemistry</topic><topic>crystals</topic><topic>dehydrogenation</topic><topic>electron microscopy</topic><topic>ethane</topic><topic>Ethane ODH</topic><topic>Ethane oxidation</topic><topic>Ethylene</topic><topic>evaporation</topic><topic>Exact sciences and technology</topic><topic>General and physical chemistry</topic><topic>infrared spectroscopy</topic><topic>isotopes</topic><topic>nickel</topic><topic>Nickel oxide</topic><topic>nitrates</topic><topic>oxides</topic><topic>surface area</topic><topic>Surface physical chemistry</topic><topic>temperature</topic><topic>Theory of reactions, general kinetics. Catalysis. Nomenclature, chemical documentation, computer chemistry</topic><topic>tin</topic><topic>Tin oxide</topic><topic>X-ray diffraction</topic><topic>X-ray photoelectron spectroscopy</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Solsona, B.</creatorcontrib><creatorcontrib>Concepción, P.</creatorcontrib><creatorcontrib>Demicol, B.</creatorcontrib><creatorcontrib>Hernández, S.</creatorcontrib><creatorcontrib>Delgado, J.J.</creatorcontrib><creatorcontrib>Calvino, J.J.</creatorcontrib><creatorcontrib>López Nieto, J.M.</creatorcontrib><collection>AGRIS</collection><collection>Pascal-Francis</collection><collection>CrossRef</collection><jtitle>Journal of catalysis</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Solsona, B.</au><au>Concepción, P.</au><au>Demicol, B.</au><au>Hernández, S.</au><au>Delgado, J.J.</au><au>Calvino, J.J.</au><au>López Nieto, J.M.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Selective oxidative dehydrogenation of ethane over SnO2-promoted NiO catalysts</atitle><jtitle>Journal of catalysis</jtitle><date>2012-11-01</date><risdate>2012</risdate><volume>295</volume><spage>104</spage><epage>114</epage><pages>104-114</pages><issn>0021-9517</issn><eissn>1090-2694</eissn><coden>JCTLA5</coden><abstract>Sn-doped NiO catalysts are highly efficient for the oxidative dehydrogenation of ethane. Addition of a tiny amount of tin highly increases selectivity to ethylene. [Display omitted]
► NiSnO mixed oxides catalysts for ethane ODH were prepared and investigated. ► Addition of a tiny amount of tin highly increases selectivity to ethylene. ► Changes in the nature of Ni species on the surface of catalysts are observed. ► Changes in the crystal size of NiO particles with Sn-loading are observed.
NiSnO mixed oxides catalysts have been investigated for the oxidative dehydrogenation of ethane. The catalysts were prepared through the evaporation of aqueous solutions of nickel nitrate and tin oxalate and finally calcined in air at 500°C for 2h. These materials have been characterized by several techniques (N2-adsorption, X-ray diffraction, High-Resolution Electron Microscopy, temperature programmed reduction, X-Ray Photoelectron Spectroscopy, Fourier Transformed Infrared Spectroscopy of adsorbed CO and 18O/16O isotope exchange). The addition of just a tiny amount of tin highly increases the selectivity to ethylene (from ca. 40% to 80–90%). Thus, high selectivity to ethylene (near to 90%) is observed on samples with high Ni/Sn atomic ratios (3<Ni/Sn<50), in which no influence of ethane conversion on selectivity to ethylene is observed (suggesting high stability of ethylene on these catalysts). Additionally, for low Sn-loadings, an increase in the catalytic activity has also been observed. The enhanced catalytic properties have been explained in terms of changes in the nature of Ni species on the catalyst surface, which can be considered as the active sites. The nature of Ni species is related to changes in the crystal size of NiO particles (and surface area) of catalysts as well as to the presence of SnOx crystals. In addition, the role of the presence of acid sites on the catalyst surface on the selectivity to ethylene is also discussed.</abstract><cop>Amsterdam</cop><pub>Elsevier Inc</pub><doi>10.1016/j.jcat.2012.07.028</doi><tpages>11</tpages></addata></record> |
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| subjects | active sites air aqueous solutions Catalysis Catalyst characterization (XPS, HREM, oxygen isotope exchange, FTIR CO adsorbed) Catalysts catalytic activity Catalytic oxidation Chemical reactions Chemistry crystals dehydrogenation electron microscopy ethane Ethane ODH Ethane oxidation Ethylene evaporation Exact sciences and technology General and physical chemistry infrared spectroscopy isotopes nickel Nickel oxide nitrates oxides surface area Surface physical chemistry temperature Theory of reactions, general kinetics. Catalysis. Nomenclature, chemical documentation, computer chemistry tin Tin oxide X-ray diffraction X-ray photoelectron spectroscopy |
| title | Selective oxidative dehydrogenation of ethane over SnO2-promoted NiO catalysts |
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