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Article: Methane emissions abatement by multi-ion-exchanged zeolite A prepared from both commercial-grade zeolite and coal fly ash

TitleMethane emissions abatement by multi-ion-exchanged zeolite A prepared from both commercial-grade zeolite and coal fly ash
Authors
Issue Date2008
Citation
Environmental Science and Technology, 2008, v. 42, n. 19, p. 7392-7397 How to Cite?
AbstractThe performance of multimetal-(Cu, Cr, Zn, Ni, and Co)-ion-exchanged zeolite A prepared from both a commercial-grade sample and one produced from coal fly ash in methane emissions abatement was evaluated in this study. The ion-exchange process was used to load the metal ions in zeolite A samples. The methane conversion efficiency by the samples was studied under various parameters including the amount of metal loading (7.3-19.4 wt%), reaction temperature (25-500°C), space velocity (8400-41 900 h-1), and methane concentration (0.5-3.2 vol %). At 500°C, the original commercial-grade zeolite A catalyzed 3% of the methane only, whereas the addition of different percentages of metals in the sample enhanced the methane conversion efficiency by 40-85%. Greater methane conversion was observed by increasing the percentage of metals added to the zeolite even though the BET surface area of the zeolite consequently decreased. Higher percentage methane conversion over the multi-ion-exchanged samples was observed at lower space velocities indicating the importance of the mass diffusion of reactants and products in the zeolite. Compared to the multi-ion-exchanged zeolite A prepared from the commercial-grade zeolite, the one produced from coal fly ash demonstrated similar performances in methane emissions abatement, showing the potential use of this low cost recycled material in gaseous pollutant treatment. © 2008 American Chemical Society.
Persistent Identifierhttp://hdl.handle.net/10722/255837
ISSN
2021 Impact Factor: 11.357
2020 SCImago Journal Rankings: 2.851
ISI Accession Number ID

 

DC FieldValueLanguage
dc.contributor.authorHui, K. S.-
dc.contributor.authorChao, C. Y.H.-
dc.date.accessioned2018-07-16T06:13:49Z-
dc.date.available2018-07-16T06:13:49Z-
dc.date.issued2008-
dc.identifier.citationEnvironmental Science and Technology, 2008, v. 42, n. 19, p. 7392-7397-
dc.identifier.issn0013-936X-
dc.identifier.urihttp://hdl.handle.net/10722/255837-
dc.description.abstractThe performance of multimetal-(Cu, Cr, Zn, Ni, and Co)-ion-exchanged zeolite A prepared from both a commercial-grade sample and one produced from coal fly ash in methane emissions abatement was evaluated in this study. The ion-exchange process was used to load the metal ions in zeolite A samples. The methane conversion efficiency by the samples was studied under various parameters including the amount of metal loading (7.3-19.4 wt%), reaction temperature (25-500°C), space velocity (8400-41 900 h-1), and methane concentration (0.5-3.2 vol %). At 500°C, the original commercial-grade zeolite A catalyzed 3% of the methane only, whereas the addition of different percentages of metals in the sample enhanced the methane conversion efficiency by 40-85%. Greater methane conversion was observed by increasing the percentage of metals added to the zeolite even though the BET surface area of the zeolite consequently decreased. Higher percentage methane conversion over the multi-ion-exchanged samples was observed at lower space velocities indicating the importance of the mass diffusion of reactants and products in the zeolite. Compared to the multi-ion-exchanged zeolite A prepared from the commercial-grade zeolite, the one produced from coal fly ash demonstrated similar performances in methane emissions abatement, showing the potential use of this low cost recycled material in gaseous pollutant treatment. © 2008 American Chemical Society.-
dc.languageeng-
dc.relation.ispartofEnvironmental Science and Technology-
dc.titleMethane emissions abatement by multi-ion-exchanged zeolite A prepared from both commercial-grade zeolite and coal fly ash-
dc.typeArticle-
dc.description.naturelink_to_subscribed_fulltext-
dc.identifier.doi10.1021/es801099y-
dc.identifier.pmid18939576-
dc.identifier.scopuseid_2-s2.0-54849190600-
dc.identifier.volume42-
dc.identifier.issue19-
dc.identifier.spage7392-
dc.identifier.epage7397-
dc.identifier.isiWOS:000259603700059-
dc.identifier.issnl0013-936X-

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