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Conference Paper: Performance of transition metal ions exchanged zeolite 13X in greenhouse gas reduction

TitlePerformance of transition metal ions exchanged zeolite 13X in greenhouse gas reduction
Authors
KeywordsMethane
Transition ions
Zeolite 13X
Catalytic combustion
Greenhouse gas
Issue Date2008
Citation
ASME International Mechanical Engineering Congress and Exposition, Proceedings, 2008, v. 15, p. 101-106 How to Cite?
AbstractThis study investigated the performance of multi-transition metal (Cu, Cr, Ni and Co) ions exchanged zeolite 13X catalysts on methane emission abatement, especially at methane level of the exhaust from natural gas fueled vehicles. Catalytic activity of methane combustion using multi-ions exchanged catalyst was studied under different parameters: mole % of metal loading, inlet velocity and inlet methane concentration at atmospheric pressure and 500°C. Performance of the catalysts was investigated and explained in terms of the apparent activation energy, number of active sites and BET surface area of the catalyst. This study showed that the multi-ions exchanged catalyst outperformed the single-ions exchanged and the acidified 13X catalysts. Lengthening the residence time could also lead to higher methane conversion %. Catalytic activity of the catalysts was influenced by the mole % of metal loading which played important roles in affecting the apparent activation energy of methane combustion, active sites and also the BET surface area of the catalyst. Increasing mole % of metal loading in the catalyst decreased the apparent activation energy for methane combustion and also the BET surface area of the catalyst. In view of these, there existed an optimized mole % of metal loading where the highest catalytic activity was observed. Copyright © 2007 by ASME.
Persistent Identifierhttp://hdl.handle.net/10722/255893

 

DC FieldValueLanguage
dc.contributor.authorHui, K. S.-
dc.contributor.authorChao, Christopher Y.H.-
dc.contributor.authorKwong, C. W.-
dc.contributor.authorWan, M. P.-
dc.date.accessioned2018-07-16T06:13:58Z-
dc.date.available2018-07-16T06:13:58Z-
dc.date.issued2008-
dc.identifier.citationASME International Mechanical Engineering Congress and Exposition, Proceedings, 2008, v. 15, p. 101-106-
dc.identifier.urihttp://hdl.handle.net/10722/255893-
dc.description.abstractThis study investigated the performance of multi-transition metal (Cu, Cr, Ni and Co) ions exchanged zeolite 13X catalysts on methane emission abatement, especially at methane level of the exhaust from natural gas fueled vehicles. Catalytic activity of methane combustion using multi-ions exchanged catalyst was studied under different parameters: mole % of metal loading, inlet velocity and inlet methane concentration at atmospheric pressure and 500°C. Performance of the catalysts was investigated and explained in terms of the apparent activation energy, number of active sites and BET surface area of the catalyst. This study showed that the multi-ions exchanged catalyst outperformed the single-ions exchanged and the acidified 13X catalysts. Lengthening the residence time could also lead to higher methane conversion %. Catalytic activity of the catalysts was influenced by the mole % of metal loading which played important roles in affecting the apparent activation energy of methane combustion, active sites and also the BET surface area of the catalyst. Increasing mole % of metal loading in the catalyst decreased the apparent activation energy for methane combustion and also the BET surface area of the catalyst. In view of these, there existed an optimized mole % of metal loading where the highest catalytic activity was observed. Copyright © 2007 by ASME.-
dc.languageeng-
dc.relation.ispartofASME International Mechanical Engineering Congress and Exposition, Proceedings-
dc.subjectMethane-
dc.subjectTransition ions-
dc.subjectZeolite 13X-
dc.subjectCatalytic combustion-
dc.subjectGreenhouse gas-
dc.titlePerformance of transition metal ions exchanged zeolite 13X in greenhouse gas reduction-
dc.typeConference_Paper-
dc.description.naturelink_to_subscribed_fulltext-
dc.identifier.doi10.1115/IMECE2007-41360-
dc.identifier.scopuseid_2-s2.0-44349127392-
dc.identifier.volume15-
dc.identifier.spage101-
dc.identifier.epage106-

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