NOx storage and reduction over copper-based catalysts. Part 2: Ce0.8M0.2Oδ supports (M = Zr, La, Ce, Pr or Nd)

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Campo DCValorIdioma
dc.contributorMateriales Carbonosos y Medio Ambientees_ES
dc.contributor.authorBueno López, Agustín-
dc.contributor.authorLozano-Castello, Dolores-
dc.contributor.authorAnderson, James A.-
dc.contributor.otherUniversidad de Alicante. Departamento de Química Inorgánicaes_ES
dc.contributor.otherUniversidad de Alicante. Instituto Universitario de Materialeses_ES
dc.date.accessioned2016-06-20T10:35:52Z-
dc.date.available2016-06-20T10:35:52Z-
dc.date.issued2016-12-05-
dc.identifier.citationApplied Catalysis B: Environmental. 2016, 198: 234-242. doi:10.1016/j.apcatb.2016.05.066es_ES
dc.identifier.issn0926-3373 (Print)-
dc.identifier.issn1873-3883 (Online)-
dc.identifier.urihttp://hdl.handle.net/10045/56034-
dc.description.abstract5% copper catalysts with Ce0.8M0.2Oδ supports (M = Zr, La, Ce, Pr or Nd) have been studied by rapid-scan operando DRIFTS for NOx Storage and Reduction (NSR) with high frequency (30 s) CO, H2 and 50%CO + 50%H2 micropulses. In the absence of reductant pulses, below 200–250 °C NOx was stored on the catalysts as nitrite and nitro groups, and above this temperature nitrates were the main species identified. The thermal stability of the NOx species stored on the catalysts depended on the acid/basic character of the dopant (M more acidic = NOx stored less stable ⇒ Zr4+ < none < Nd3+ < Pr3+ < La3+ ⇐ M more basic = NOx stored more stable). Catalysts regeneration was more efficient with H2 than with CO, and the CO + H2 mixture presented an intermediate behavior, but with smaller differences among the series of catalyst than observed using CO alone. N2 is the main NOx reduction product upon H2 regeneration. The highest NOx removal in NSR experiments performed at 400 °C with CO + H2 pulses was achieved with the catalyst with the most basic dopant (CuO/Ce0.8La0.2Oδ) while the poorest performing catalyst was that with the most acidic dopant (CuO/Ce0.8Zr0.2Oδ). The poor performance of CuO/Ce0.8Zr0.2Oδ in NSR experiments with CO pulses was attributed to its lower oxidation capacity compared to the other catalysts.es_ES
dc.description.sponsorshipThe authors thank the financial support of Generalitat Valenciana (Project PROMETEOII/2014/010 and grant BEST/2014/250),the Spanish Ministry of Economy and Competitiveness (ProjectsCTQ2015-67597-C2-2-R, MAT2014-61992-EXP, and grantPRX14/00249), and the UE (FEDER funding).es_ES
dc.languageenges_ES
dc.publisherElsevieres_ES
dc.rights© 2016 Published by Elsevier B.V.es_ES
dc.subjectNSRes_ES
dc.subjectdeNOxes_ES
dc.subjectDiesel aftertreatmentes_ES
dc.subjectCopper catalystes_ES
dc.subjectCeriaes_ES
dc.subjectDRIFTSes_ES
dc.subjectOperandoes_ES
dc.subject.otherQuímica Inorgánicaes_ES
dc.titleNOx storage and reduction over copper-based catalysts. Part 2: Ce0.8M0.2Oδ supports (M = Zr, La, Ce, Pr or Nd)es_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
dc.peerreviewedsies_ES
dc.identifier.doi10.1016/j.apcatb.2016.05.066-
dc.relation.publisherversionhttp://dx.doi.org/10.1016/j.apcatb.2016.05.066es_ES
dc.rights.accessRightsinfo:eu-repo/semantics/openAccesses_ES
dc.relation.projectIDinfo:eu-repo/grantAgreement/MINECO//CTQ2015-67597-C2-2-R-
dc.relation.projectIDinfo:eu-repo/grantAgreement/MINECO//MAT2014-61992-EXP-
dc.relation.projectIDinfo:eu-repo/grantAgreement/MECD//PRX14%2F00249-
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