Please use this identifier to cite or link to this item: http://hdl.handle.net/10397/111728
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dc.contributorDepartment of Applied Physics-
dc.creatorHerrera, Jen_US
dc.creatorAguila, Gen_US
dc.creatorZhu, Yen_US
dc.creatorXu, Zen_US
dc.creatorGuerrero, Ruz, Sen_US
dc.date.accessioned2025-03-13T02:25:01Z-
dc.date.available2025-03-13T02:25:01Z-
dc.identifier.issn2470-1343en_US
dc.identifier.urihttp://hdl.handle.net/10397/111728-
dc.language.isoenen_US
dc.publisherAmerican Chemical Societyen_US
dc.rightsThis article is licensed under CC-BY-NC-ND 4.0 (https://creativecommons.org/licenses/by-nc-nd/4.0/)en_US
dc.rights© 2024 The Authors. Published byAmerican Chemical Societyen_US
dc.rightsThe following publication Herrera, J., Aguila, G., Zhu, Y., Xu, Z., & Guerrero Ruz, S. (2024). Calcium-Poison-Resistant Cu/YCeO2–TiO2 Catalyst for the Selective Catalytic Reduction of NO with CO and Naphthalene in the Presence of Oxygen. ACS Omega, 9(39), 40394-40410 is available at https://doi.org/10.1021/acsomega.4c02423.en_US
dc.titleCalcium-poison-resistant cu/yceo2-tio2 catalyst for the selective catalytic reduction of no with co and naphthalene in the presence of oxygenen_US
dc.typeJournal/Magazine Articleen_US
dc.identifier.spage40394en_US
dc.identifier.epage40410en_US
dc.identifier.volume9en_US
dc.identifier.issue39en_US
dc.identifier.doi10.1021/acsomega.4c02423en_US
dcterms.abstractThe pollution from industrial processes based on biomass combustion is still an ongoing problem. In the present contribution, the selective catalytic reduction of NO with CO and naphthalene is carried out in the presence of 10% oxygen. The accumulation of alkaline and alkaline earth metals during biomass combustion is here simulated by the addition of calcium to a Cu-impregnated YCeO2-TiO2 support. The results show that a high dispersion of copper is obtained, which is resistant to the accumulation of calcium. Full conversion of CO and naphthalene is achieved above 200 °C, whereas NO conversions of 80, 90, and 87% are obtained for the catalysts with Ca loadings of 2.6, 5.2, and 13%, respectively, at 350 °C. It is proposed that the high activity of the catalysts is ascribed to the formation of Cu-Ox-Ce species and that the accumulation of Ca acts as a barrier to avoid copper sintering. It was found that different forms of carbonate and nitrite/nitrate species form during reaction, coexisting as adsorbed species during the SCR reaction. The selectivity to N2 was almost 100% in all cases, due to the small presence of NO2 in the reactor outlet (no N2O was detected in any conditions).-
dcterms.accessRightsopen accessen_US
dcterms.bibliographicCitationACS omega, 1 Oct. 2024, v. 9, no. 39, p. 40394-40410en_US
dcterms.isPartOfACS omegaen_US
dcterms.issued2024-10-01-
dc.identifier.scopus2-s2.0-85205933034-
dc.description.validate202502 bcrc-
dc.description.oaVersion of Recorden_US
dc.identifier.FolderNumberOA_Scopus/WOS-
dc.description.fundingSourceOthersen_US
dc.description.fundingTextChilean National Science and Technology Research Funden_US
dc.description.pubStatusPublisheden_US
dc.description.oaCategoryCCen_US
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