Please use this identifier to cite or link to this item: https://scholarbank.nus.edu.sg/handle/10635/90732
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dc.titleSynthesis and characterization of nanoscale CeO 2 catalyst for deNOx
dc.contributor.authorKawi, S.
dc.contributor.authorTang, Y.P.
dc.contributor.authorHidajat, K.
dc.contributor.authorYu, L.E.
dc.date.accessioned2014-10-09T07:08:31Z
dc.date.available2014-10-09T07:08:31Z
dc.date.issued2005
dc.identifier.citationKawi, S.,Tang, Y.P.,Hidajat, K.,Yu, L.E. (2005). Synthesis and characterization of nanoscale CeO 2 catalyst for deNOx. Journal of Metastable and Nanocrystalline Materials 23 : 95-98. ScholarBank@NUS Repository.
dc.identifier.issn14226375
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/90732
dc.description.abstractHydrothermal and precipitation methods have been applied to synthesize nanoscale CeO 2 catalysts for selective catalytic reduction of NO with hydrocarbon under oxygen-rich condition. The former procedure has the advantage of enhancing the hydrothermal stability of nanomaterial. BET results show that their surface areas are about 30-80 m 2/g. Based on TEM results, hydrothermally prepared CeO 2 shows very uniform grain shaped particles with size around 10-20 nanometers. Its thermal stability up to 1200°C has been confirmed by in-situ XRD. Furthermore, deNOx reaction with propene as reducing agent in the presence of 5% oxygen has been carried out to compare catalysts prepared by the above two methods. Results show that hydrothermally prepared catalyst is more active than the one prepared by precipitation method. The latter one lost half of its activity in the presence of 5% water vapor, while the former one could stand up to 10% water vapor in the gas mixture without losing much activity.
dc.sourceScopus
dc.subjectCeria
dc.subjectDeNOx
dc.subjectHydrothermal Synthesis
dc.subjectIn Situ XRD
dc.typeConference Paper
dc.contributor.departmentCHEMICAL & BIOMOLECULAR ENGINEERING
dc.description.sourcetitleJournal of Metastable and Nanocrystalline Materials
dc.description.volume23
dc.description.page95-98
dc.identifier.isiutNOT_IN_WOS
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