Cu/Al2O3 catalysts for soot oxidation: Copper loading effect

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Títol: Cu/Al2O3 catalysts for soot oxidation: Copper loading effect
Autors: López Suárez, Franz Edwin | Bueno López, Agustín | Illán-Gómez, María José
Grups d'investigació o GITE: Materiales Carbonosos y Medioambiente
Centre, Departament o Servei: Universidad de Alicante. Departamento de Química Inorgánica
Paraules clau: Soot | NOx | Alumina | Copper catalyst
Àrees de coneixement: Química Inorgánica
Data de creació: de març-2008
Data de publicació: de desembre-2008
Editor: Elsevier
Citació bibliogràfica: LÓPEZ SUÁREZ, Franz Edwin; BUENO LÓPEZ, Agustín; ILLÁN GÓMEZ, María José. "Cu/Al2O3 catalysts for soot oxidation: Copper loading effect". Applied Catalysis B: Environmental. Vol. 84, Issues 3-4 (1 Dec. 2008). ISSN 0926-3373, pp. 651-658
Resum: Cu/Al2O3 catalysts with metal loading from 0.64 to 8.8 wt.% have been prepared and characterized by different techniques: N2 adsorption at −196 °C (BET surface area), ICP (Cu loading), XRD, selective copper surface oxidation with N2O (Cu dispersion), TPR-H2 (redox properties), and XPS (copper surface species). The catalytic activity for soot oxidation has been tested both in air and NOx/O2. The activity in air depends on the amount of easily-reduced Cu(II) species, which are reduced around 275 °C under TPR-H2 conditions. The amount of the most active Cu(II) species increases with the copper loading from Cu_1% to Cu_5% and remains almost constant for higher copper loading. In the presence of NOx, the first step of the mechanism is NO oxidation to NO2, and the catalytic activity for this reaction depends on the copper loading. For catalysts with copper loading between Cu_1% and Cu_5%, the catalytic activity for soot oxidation in the presence of NOx depends on NO2 formation. For catalysts with higher copper loading this trend is not followed because of the low reactivity of model soot at the temperature of maximum NO2 production. Regardless the copper loading, all the catalysts improve the selectivity towards CO2 formation as soot oxidation product both under air and NOx/O2.
Patrocinadors: MEC (project CTQ2005-01358); FELS thanks University of Alicante (International Cooperation Office) his thesis grant.
URI: http://hdl.handle.net/10045/8242
ISSN: 0926-3373
DOI: 10.1016/j.apcatb.2008.05.019
Idioma: eng
Tipus: info:eu-repo/semantics/article
Revisió científica: si
Versió de l'editor: http://dx.doi.org/10.1016/j.apcatb.2008.05.019
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