Hydrothermal deactivation of Fe-ZSM-5 catalysts for the selective catalytic reduction of NO with NH sub(3)
The hydrothermal deactivation of Fe-ZSM-5 catalysts for the reduction of NO with NH sub(3) in the presence of 10% H sub(2)O was studied. Aged and fresh catalysts were characterized by H-TPR, DRIFTS, super(27)Al NMR, super(29)Si NMR, XAS and nitrogen physisorption. The analysis of deactivated catalys...
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Veröffentlicht in: | Applied catalysis. B, Environmental Environmental, 2011-01, Vol.101 (3-4), p.649-659 |
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description | The hydrothermal deactivation of Fe-ZSM-5 catalysts for the reduction of NO with NH sub(3) in the presence of 10% H sub(2)O was studied. Aged and fresh catalysts were characterized by H-TPR, DRIFTS, super(27)Al NMR, super(29)Si NMR, XAS and nitrogen physisorption. The analysis of deactivated catalysts indicated that, under moderately aging conditions, dealumination due to hydrolysis occurs only on Al sites that bear a Broensted acidic proton. Furthermore, the results showed that the cause of hydrothermal aging is Fe migration, which leads to the formation of FeO sub(x) clusters that increase in size as the age of the catalyst increases. This Fe migration was not strongly related to the process of dealumination and the stability with respect to SCR activity depends more on the stability of the active iron species in ion exchange sites than the stability of the framework itself. The hydrothermal stability of these active iron sites was not significantly influenced by the presence of Broensted acid protons. The remaining activity after hydrothermal aging is caused by isolated iron ions located at ion exchange sites. Based on these results a general mechanism for aging under hydrothermal conditions was developed that differentiates between dealumination, migration and clustering of Fe oxides and the temporal sequence of these processes. |
doi_str_mv | 10.1016/j.apcatb.2010.11.006 |
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Aged and fresh catalysts were characterized by H-TPR, DRIFTS, super(27)Al NMR, super(29)Si NMR, XAS and nitrogen physisorption. The analysis of deactivated catalysts indicated that, under moderately aging conditions, dealumination due to hydrolysis occurs only on Al sites that bear a Broensted acidic proton. Furthermore, the results showed that the cause of hydrothermal aging is Fe migration, which leads to the formation of FeO sub(x) clusters that increase in size as the age of the catalyst increases. This Fe migration was not strongly related to the process of dealumination and the stability with respect to SCR activity depends more on the stability of the active iron species in ion exchange sites than the stability of the framework itself. The hydrothermal stability of these active iron sites was not significantly influenced by the presence of Broensted acid protons. The remaining activity after hydrothermal aging is caused by isolated iron ions located at ion exchange sites. Based on these results a general mechanism for aging under hydrothermal conditions was developed that differentiates between dealumination, migration and clustering of Fe oxides and the temporal sequence of these processes.</description><identifier>ISSN: 0926-3373</identifier><identifier>DOI: 10.1016/j.apcatb.2010.11.006</identifier><language>eng</language><subject>Aluminum ; Catalysis ; Catalysts ; Deactivation ; Iron ; Migration ; Nuclear magnetic resonance ; Reduction ; Stability</subject><ispartof>Applied catalysis. 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Aged and fresh catalysts were characterized by H-TPR, DRIFTS, super(27)Al NMR, super(29)Si NMR, XAS and nitrogen physisorption. The analysis of deactivated catalysts indicated that, under moderately aging conditions, dealumination due to hydrolysis occurs only on Al sites that bear a Broensted acidic proton. Furthermore, the results showed that the cause of hydrothermal aging is Fe migration, which leads to the formation of FeO sub(x) clusters that increase in size as the age of the catalyst increases. This Fe migration was not strongly related to the process of dealumination and the stability with respect to SCR activity depends more on the stability of the active iron species in ion exchange sites than the stability of the framework itself. The hydrothermal stability of these active iron sites was not significantly influenced by the presence of Broensted acid protons. The remaining activity after hydrothermal aging is caused by isolated iron ions located at ion exchange sites. Based on these results a general mechanism for aging under hydrothermal conditions was developed that differentiates between dealumination, migration and clustering of Fe oxides and the temporal sequence of these processes.</description><subject>Aluminum</subject><subject>Catalysis</subject><subject>Catalysts</subject><subject>Deactivation</subject><subject>Iron</subject><subject>Migration</subject><subject>Nuclear magnetic resonance</subject><subject>Reduction</subject><subject>Stability</subject><issn>0926-3373</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2011</creationdate><recordtype>article</recordtype><recordid>eNp9jDtPAkEYRafQRET_gcV0YrHrN--Z0hARE4RCKhsyO4-wZGFxZ1bDvxcitlY3uffcg9AdgZIAkY-b0u6dzVVJ4VSREkBeoAEYKgvGFLtC1yltAIAyqgdoMz34rs3r0G1tg32wLtdfNtftDrcRT0Lx8f5WCHw02uaQcsKx7fARxyk04cSG85Zrh7vge_f3nS_wd53XeD7Fqa9G7OEGXUbbpHB7ziFaTp6X42kxW7y8jp9mxV4KUWhnqI3cRc64ZFo67p3XggjjmKqY4F6AE0SbSCvrqaVKgDeRR-UNDTKwIbr_1e679rMPKa-2dXKhaewutH1aaSEUMM3FkRz9SxKlFGFgJLAfYK9onQ</recordid><startdate>20110114</startdate><enddate>20110114</enddate><creator>Brandenberger, Sandro</creator><creator>Kroecher, Oliver</creator><creator>Casapu, Maria</creator><creator>Tissler, Arno</creator><creator>Althoff, Roderik</creator><scope>7SR</scope><scope>7SU</scope><scope>7U5</scope><scope>8BQ</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>JG9</scope><scope>KR7</scope><scope>L7M</scope><scope>7ST</scope><scope>SOI</scope></search><sort><creationdate>20110114</creationdate><title>Hydrothermal deactivation of Fe-ZSM-5 catalysts for the selective catalytic reduction of NO with NH sub(3)</title><author>Brandenberger, Sandro ; Kroecher, Oliver ; Casapu, Maria ; Tissler, Arno ; Althoff, Roderik</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-p655-8c92af4cf4346386c4dcd85159c37b354d50c5189f2bad2a2750d9f4f7d92e6e3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2011</creationdate><topic>Aluminum</topic><topic>Catalysis</topic><topic>Catalysts</topic><topic>Deactivation</topic><topic>Iron</topic><topic>Migration</topic><topic>Nuclear magnetic resonance</topic><topic>Reduction</topic><topic>Stability</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Brandenberger, Sandro</creatorcontrib><creatorcontrib>Kroecher, Oliver</creatorcontrib><creatorcontrib>Casapu, Maria</creatorcontrib><creatorcontrib>Tissler, Arno</creatorcontrib><creatorcontrib>Althoff, Roderik</creatorcontrib><collection>Engineered Materials Abstracts</collection><collection>Environmental Engineering Abstracts</collection><collection>Solid State and Superconductivity Abstracts</collection><collection>METADEX</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>Materials Research Database</collection><collection>Civil Engineering Abstracts</collection><collection>Advanced Technologies Database with Aerospace</collection><collection>Environment Abstracts</collection><collection>Environment Abstracts</collection><jtitle>Applied catalysis. B, Environmental</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Brandenberger, Sandro</au><au>Kroecher, Oliver</au><au>Casapu, Maria</au><au>Tissler, Arno</au><au>Althoff, Roderik</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Hydrothermal deactivation of Fe-ZSM-5 catalysts for the selective catalytic reduction of NO with NH sub(3)</atitle><jtitle>Applied catalysis. B, Environmental</jtitle><date>2011-01-14</date><risdate>2011</risdate><volume>101</volume><issue>3-4</issue><spage>649</spage><epage>659</epage><pages>649-659</pages><issn>0926-3373</issn><abstract>The hydrothermal deactivation of Fe-ZSM-5 catalysts for the reduction of NO with NH sub(3) in the presence of 10% H sub(2)O was studied. Aged and fresh catalysts were characterized by H-TPR, DRIFTS, super(27)Al NMR, super(29)Si NMR, XAS and nitrogen physisorption. The analysis of deactivated catalysts indicated that, under moderately aging conditions, dealumination due to hydrolysis occurs only on Al sites that bear a Broensted acidic proton. Furthermore, the results showed that the cause of hydrothermal aging is Fe migration, which leads to the formation of FeO sub(x) clusters that increase in size as the age of the catalyst increases. This Fe migration was not strongly related to the process of dealumination and the stability with respect to SCR activity depends more on the stability of the active iron species in ion exchange sites than the stability of the framework itself. The hydrothermal stability of these active iron sites was not significantly influenced by the presence of Broensted acid protons. The remaining activity after hydrothermal aging is caused by isolated iron ions located at ion exchange sites. Based on these results a general mechanism for aging under hydrothermal conditions was developed that differentiates between dealumination, migration and clustering of Fe oxides and the temporal sequence of these processes.</abstract><doi>10.1016/j.apcatb.2010.11.006</doi><tpages>11</tpages></addata></record> |
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subjects | Aluminum Catalysis Catalysts Deactivation Iron Migration Nuclear magnetic resonance Reduction Stability |
title | Hydrothermal deactivation of Fe-ZSM-5 catalysts for the selective catalytic reduction of NO with NH sub(3) |
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