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Supported CuO+Ag/Partially Stabilized Zirconia Catalysts for the Selective Catalytic Reduction of NOx under Lean Burn Conditions: 1. Bulk and Surface Properties of the Catalysts Full article

Общее Language: Английский, Genre: Full article,
Status: Published, Source type: Original
Journal Journal of Catalysis
ISSN: 0021-9517 , E-ISSN: 1090-2694
Output data Year: 2001, Volume: 200, Number: 1, Pages: 117-130 Pages count : 14 DOI: 10.1006/jcat.2001.3193
Tags Adsorption properties, Bulk and surface structure, Characterization, CO, Mesoporosity, NOx, Partially stabilized zirconia, Silver, Supported copper oxide, Synthesis
Authors Sadykov Vladislav A. 1,2 , Bunina R.V. 1 , Alikina G.M. 1 , Ivanova A.S. 1 , Kochubey D.I. 1 , Novgorodov B.N. 1 , Paukshtis E.A. 1,2 , Fenelonov V.B. 1 , Zaikovskii V.I. 1 , Kuznetsova T.G. 1 , Beloshapkin S.A. 1,2 , Kolomiichuk V.N. 1 , Moroz E.M. 1 , Matyshak V.A. 3 , Konin G.A. 3 , Rozovskii A.Y. 4 , Ross J.R. 5 , Breen J.P. 5
Affiliations
1 Boreskov Institute of Catalysis, Siberian Branch of the Russian Academy of Sciences, Lavrentieva 5, Novosibirsk 630090, Russia
2 Novosibirsk State University, Pirogova 1, Novosibirsk 630090, Russia
3 Semenov Institute of Chemical Physics RAS, Moscow, Russia
4 Topchiev Institute of Petrochemical Synthesis RAS, Moscow, Russia
5 University of Limerick, Limerick, Ireland

Funding (1)

1 International Association for the Promotion of Co-operation with Scientists from the New Independent States of the Former Soviet Union 97-11720

Abstract: Thermally stable cubic mesoporous zirconia samples stabilized by the alkaline-earth cations (Ca, Sr, Ba) were synthesized via the coprecipitation route followed by refluxing in the presence of surfactants. These systems were used as supports for copper cations and then modified by the addition of silver nanoparticles using impregnation or photoassisted deposition techniques. The structural, textural, and surface features of these nanosystems were studied by using TEM, X-ray diffraction, EXAFS, nitrogen adsorption isotherms, SAXS, FTIRS of adsorbed CO, and TPD of adsorbed NOx species. Partially stabilized zirconia samples were found to possess a disordered cubic structure. A higher tendency of bulky Ba cation to segregate in the surface layer is reflected in a higher degree of surface disordering, higher concentration of hydroxyls, and greater coordination unsaturation of isolated copper cations. In contrast to such traditional supports as γ-alumina, stabilized zirconia supports appear to favor formation of small reactive (probably, three-dimensional) clusters of copper cations possessing an increased reactivity and decreased strength of oxygen bonding with these cations. It is reflected in decreased thermal stability of surface nitrite and nitrate species located at these centers as compared with such species on the surface of CuO/alumina catalysts. This feature seems to be primarily determined by the specificity of the surface structure of fluorite-like supports (ceria, zirconia). Silver incorporation into copper oxidic clusters decreases the strength of copper–oxygen bonds as well as the thermal stability of adsorbed nitrite–nitrate species. For samples prepared via the photodeposition route, the clustering degree of copper cations is usually lower than in the case of samples obtained by traditional impregnation procedure.
Cite: Sadykov V.A. , Bunina R.V. , Alikina G.M. , Ivanova A.S. , Kochubey D.I. , Novgorodov B.N. , Paukshtis E.A. , Fenelonov V.B. , Zaikovskii V.I. , Kuznetsova T.G. , Beloshapkin S.A. , Kolomiichuk V.N. , Moroz E.M. , Matyshak V.A. , Konin G.A. , Rozovskii A.Y. , Ross J.R. , Breen J.P.
Supported CuO+Ag/Partially Stabilized Zirconia Catalysts for the Selective Catalytic Reduction of NOx under Lean Burn Conditions: 1. Bulk and Surface Properties of the Catalysts
Journal of Catalysis. 2001. V.200. N1. P.117-130. DOI: 10.1006/jcat.2001.3193 publication_identifier_short.wos_identifier_type publication_identifier_short.scopus_identifier_type publication_identifier_short.rinz_identifier_type
Dates:
Submitted: Oct 6, 2000
Accepted: Feb 2, 2001
Published online: Apr 11, 2001
Published print: May 1, 2001
Identifiers:
publication_identifier.wos_identifier_type WOS:000168939800013
publication_identifier.scopus_identifier_type 2-s2.0-0035527139
publication_identifier.rinz_identifier_type 13380828
publication_identifier.accession_number_identifier_type 2001:305613
publication_identifier.chemical_accession_number_identifier_type 135:111200
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