In situ sulphated CuOx/ZrO2 and CuOx/sulphated-ZrO2 as catalysts for the reduction of NOx with NH3 in the presence of excess O2 (Articolo in rivista)

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  • In situ sulphated CuOx/ZrO2 and CuOx/sulphated-ZrO2 as catalysts for the reduction of NOx with NH3 in the presence of excess O2 (Articolo in rivista) (literal)
Anno
  • 2005-01-01T00:00:00+01:00 (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#doi
  • 10.1016/j.apcatb.2005.02.025 (literal)
Alternative label
  • Pietrogiacomi D., Magliano A., Sannino D., Campa M.C., Ciambelli P., Indovina V. (2005)
    In situ sulphated CuOx/ZrO2 and CuOx/sulphated-ZrO2 as catalysts for the reduction of NOx with NH3 in the presence of excess O2
    in Applied catalysis. B, Environmental (Print); Elsevier, Amsterdam (Paesi Bassi)
    (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#autori
  • Pietrogiacomi D., Magliano A., Sannino D., Campa M.C., Ciambelli P., Indovina V. (literal)
Pagina inizio
  • 83 (literal)
Pagina fine
  • 92 (literal)
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  • http://www.sciencedirect.com/science/article/pii/S0926337305001232 (literal)
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  • 60 (literal)
Rivista
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  • fasc. (1-2). Elsevier. (literal)
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  • 10 (literal)
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  • 1-2 (literal)
Note
  • ISI Web of Science (WOS) (literal)
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  • a) Dipartimento di Chimica, Università degli Studi di Roma \"La Sapienza\", Piazzale Aldo Moro 5, 00185 Rome, Italy b) Dipartimento di Ingegneria Chimica e Alimentare, Università di Salerno, 84084 Fisciano (Salerno), Italy. c) Sezione ''MICE'' dell'Istituto I.S.C. (CNR), c/o Dipartimento di Chimica, Universita` di Roma ''La Sapienza'', Piazzale Aldo Moro 5, 00185 Roma, Italy (literal)
Titolo
  • In situ sulphated CuOx/ZrO2 and CuOx/sulphated-ZrO2 as catalysts for the reduction of NOx with NH3 in the presence of excess O2 (literal)
Abstract
  • Sulphated catalysts containing the same amount of sulphates (2.6 SO4 nm-2) and a different amount of copper (0.3-3.9 Cu atoms nm-2), Cu/SZ, were prepared by impregnation of sulphated-ZrO2 with toluene solutions of Cu(acetylacetonate)2. Sulphated catalysts containing the same amount of copper (0.3 or 2.5 atoms nm-2) and a different amount of sulphates (up to 4.9 SO2 nm-2), Cu/ZSg, were prepared by sulphation of CuOx/ZrO2 (Cu/Z) via the gas-phase. Samples were characterised by Fourier transformed IR spectroscopy. The selective catalytic reduction of NO with NH3 in the presence of excess O2 (SCR reaction), the NH3 + O2 and the NO + O2 reactions were studied in a flow apparatus. Activity and selectivity did not depend on the sulphation method used for catalyst preparation but depended on the amount of copper and sulphate, particularly on the sulphate/copper ratio. As on Cu/Z, on Cu/SZ CuII was active for both SCR and NH3 + O2 reactions. The presence of covalent sulphates caused lower reducibility of CuII to CuI and higher Lewis acid strength of CuI in Cu/SZ than in Cu/Z. For (i) SCR, (ii) NH3 + O2 and (iii) NO + O2, Cu/ZSg were less active than the parent Cu/Z. As the sulphate content in Cu/ZSg increased, the NO yield in the NH3 + O2 reaction markedly decreased, thus accounting for the increased selectivity in the SCR reaction. In CuOx/sulphated-ZrO2 copper ions were less prone reversibly to undergo the redox process CuII/CuI. These findings provide new information on the role of copper and sulphate in determining the activity and selectivity for the SCR with NH3. (literal)
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