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Catalysts for NOx selective catalytic reduction by hydrocarbons (HC-SCR)

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dc.contributor.author Mrad, Raya
dc.contributor.author Aissat, Aissa
dc.contributor.author Cousin, Renaud
dc.contributor.author Courcot, Dominique
dc.contributor.author Siffert, Stéphane
dc.date.accessioned 2025-01-24T11:21:45Z
dc.date.available 2025-01-24T11:21:45Z
dc.date.issued 2015
dc.identifier.uri http://hdl.handle.net/10938/25305
dc.description.abstract This short review concerns the efficient catalysts for HC-SCR discovered more than 20 years ago. In 1990, Iwamoto proposed Cu ion-exchanged ZSM-5, and it was the first powerful catalyst for HC-SCR. This paper presents first metal ion-exchanged zeolites and the influence of various parameters on the catalysts activities (acidity, O2 content, etc.). In the second part, this paper reviews supported metal catalysts, base metal oxides, hybrid catalysts and the possible reducing agents to remove NOx. It can be inferred that the most active catalysts for HC-SCR should have acidic sites, an active phase like copper or cobalt, or for a wider activity, elements such as silver or a mixture of metals. For low deactivation, they should contain noble metals such as platinum, rhodium or tin. © 2014 Elsevier B.V. All rights reserved.
dc.language.iso en
dc.publisher Elsevier B.V.
dc.relation.ispartof Applied Catalysis A: General
dc.source Scopus
dc.subject Hc-scr
dc.subject Minireview
dc.subject Nox
dc.subject Reduction by hydrocarbons
dc.subject Catalyst activity
dc.subject Heavy ions
dc.subject Hydrocarbons
dc.subject Ion exchange
dc.subject Metal ions
dc.subject Metals
dc.subject Nitrogen oxides
dc.subject Reducing agents
dc.subject Zeolites
dc.subject Acidic sites
dc.subject Active catalyst
dc.subject Base metals
dc.subject Efficient catalysts
dc.subject Hybrid catalysts
dc.subject Ion exchanged zeolites
dc.subject Supported-metal catalysts
dc.subject Selective catalytic reduction
dc.title Catalysts for NOx selective catalytic reduction by hydrocarbons (HC-SCR)
dc.type Article
dc.contributor.department Department of Chemistry
dc.contributor.faculty Faculty of Arts and Sciences (FAS)
dc.contributor.institution American University of Beirut
dc.identifier.doi https://doi.org/10.1016/j.apcata.2014.10.021
dc.identifier.eid 2-s2.0-84942279759


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