Please use this identifier to cite or link to this item:
https://hdl.handle.net/20.500.14279/11035
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Costa, Costas | - |
dc.contributor.author | Efstathiou, A. M. | - |
dc.contributor.author | Stathopoulos, V. N. | - |
dc.contributor.author | Belessi, Vassiliki | - |
dc.date.accessioned | 2018-05-10T09:08:45Z | - |
dc.date.available | 2018-05-10T09:08:45Z | - |
dc.date.issued | 2001-01-25 | - |
dc.identifier.citation | Journal of Catalysis, 2001, vol. 197, no. 2, pp. 350-364 | en_US |
dc.identifier.issn | 00219517 | - |
dc.identifier.uri | https://hdl.handle.net/20.500.14279/11035 | - |
dc.description.abstract | The NO/H2/O2 reaction has been studied under lean-burn conditions in the 100-400°C range over 0.1 wt% Pt supported on La0.5Ce0.5MnO3 (mixed oxide containing LaMnO3, CeO2, and MnO2 phases). For a critical comparison, 0.1 wt% Pt was supported on γ-Al2O3 and tested under the same reaction conditions. The maximum in the NO conversion has been observed at 140°C (74% conversion) for the Pt/La0.5Ce0.5MnO3 and at 125°C (66% conversion) for the Pt/γ3-Al2O3 catalyst using a GHSV of 80, 000 h−1. Addition of 5% H2O in the feed stream influenced the performance of the catalyst in a positive way. In particular, it widened the operating temperature window of the catalyst above 200°C with appreciable NO conversion and had no negative effect on the stability of the catalyst for a 20-h run on reaction stream. Remarkable N2 selectivity values in the 80-90% range have been observed on the Pt/La0.5Ce0.5MnO3 catalyst in the 100-200°C range either in the absence or in the presence of water in the feed stream. This result is reported for the first time for the NO/H2/O2 lean-deNOx reaction at least on Pt-based catalysts. A maximum specific integral reaction rate of 397 μmol of N2/s.g of Pt metal was measured at 140°C during reaction with 0.25% NO/1% H2/5% O2/5% H2O/He gas mixture on the 0.1 wt% Pt/La0.5Ce0.5MnO3 catalyst. This value was found to be higher by 40% than that observed on the 0.1 wt% Pt/γ-Al2O3 catalyst at 125°C, and it is the highest value ever reported in the 100-200°C range. A TOF value of 0.49 s−1 was calculated at 140°C for the Pt/La0.5Ce0.5MnO3 catalyst. Temperature-programmed desorption (TPD) of NO and transient titration experiments of the catalyst surface following reaction have revealed important information concerning several mechanistic steps of the present catalytic system. A hydrogen-assisted NO dissociation step and a nitrogen-assisted mechanism for N2 and N2O formation are proposed to explain all the transient experiments performed in a satisfactory manner. | en_US |
dc.format | en_US | |
dc.language.iso | en | en_US |
dc.relation.ispartof | Journal of Catalysis | en_US |
dc.rights | © Elsevier | en_US |
dc.rights | Attribution-NonCommercial-NoDerivs 3.0 United States | * |
dc.rights.uri | http://creativecommons.org/licenses/by-nc-nd/3.0/us/ | * |
dc.subject | Lean de-NOx | en_US |
dc.subject | NO reduction | en_US |
dc.subject | NO TPD | en_US |
dc.subject | Perovskites | en_US |
dc.title | An investigation of the NO/H2/O2 (Lean-deNOx) reaction on a highly active and selective Pt/La0.5Ce0.5MnO3 catalyst | en_US |
dc.type | Article | en_US |
dc.collaboration | University of Cyprus | en_US |
dc.collaboration | University of Ioannina | en_US |
dc.subject.category | Chemical Sciences | en_US |
dc.country | Greece | en_US |
dc.country | Cyprus | en_US |
dc.subject.field | Natural Sciences | en_US |
dc.publication | Peer Reviewed | en_US |
dc.identifier.doi | 10.1006/jcat.2000.3101 | en_US |
dc.relation.issue | 2 | en_US |
dc.relation.volume | 197 | en_US |
cut.common.academicyear | 2000-2001 | en_US |
dc.identifier.spage | 350 | en_US |
dc.identifier.epage | 364 | en_US |
item.openairetype | article | - |
item.cerifentitytype | Publications | - |
item.fulltext | No Fulltext | - |
item.grantfulltext | none | - |
item.openairecristype | http://purl.org/coar/resource_type/c_6501 | - |
item.languageiso639-1 | en | - |
crisitem.author.dept | Department of Chemical Engineering | - |
crisitem.author.faculty | Faculty of Geotechnical Sciences and Environmental Management | - |
crisitem.author.orcid | 0000-0002-8459-0356 | - |
crisitem.author.parentorg | Faculty of Geotechnical Sciences and Environmental Management | - |
crisitem.journal.journalissn | 0021-9517 | - |
crisitem.journal.publisher | Elsevier | - |
Appears in Collections: | Άρθρα/Articles |
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