Copper-ion exchanged Ti-pillared clays for selective catalytic reduction of NO by propylene
dc.contributor.author | Lu, G. | |
dc.contributor.author | Li, Xin Yong | |
dc.contributor.author | Qu, Z. | |
dc.contributor.author | Zhao, Q. | |
dc.contributor.author | Zhao, L. | |
dc.contributor.author | Chen, G. | |
dc.date.accessioned | 2017-01-30T10:30:16Z | |
dc.date.available | 2017-01-30T10:30:16Z | |
dc.date.created | 2015-10-29T04:09:55Z | |
dc.date.issued | 2011 | |
dc.identifier.citation | Lu, G. and Li, X. and Qu, Z. and Zhao, Q. and Zhao, L. and Chen, G. 2011. Copper-ion exchanged Ti-pillared clays for selective catalytic reduction of NO by propylene. Chemical Engineering Journal. 168 (3): pp. 1128-1133. | |
dc.identifier.uri | http://hdl.handle.net/20.500.11937/3335 | |
dc.identifier.doi | 10.1016/j.cej.2011.01.095 | |
dc.description.abstract |
Cu-ion-exchanged titanium-pillared clays (Cu-Ti-PILCs) were prepared using ion exchange strategy under different pH values and used for selective catalytic reduction (SCR) of NO by propylene. The influences of pH value on the catalytic performance and the nature of copper species were investigated. The results of activity test showed that the highest conversion of NO into N2 and the low-temperature activity increased with the increase of pH value up to 6, and then decreased with the further increase of pH value. The characterization results showed that the copper species were well dispersed over the prepared catalysts, and the different ratios of Cu2+/copper species existed over the studied catalysts. The Cu2+ species can enhance the low-temperature activity and the highest conversion of NO into N2. Moreover, the highest conversion of NO into N2 and low-temperature activity increased with the increase of the Cu2+/copper species rate. © 2011 Elsevier B.V. | |
dc.title | Copper-ion exchanged Ti-pillared clays for selective catalytic reduction of NO by propylene | |
dc.type | Journal Article | |
dcterms.source.volume | 168 | |
dcterms.source.number | 3 | |
dcterms.source.startPage | 1128 | |
dcterms.source.endPage | 1133 | |
dcterms.source.issn | 1385-8947 | |
dcterms.source.title | Chemical Engineering Journal | |
curtin.department | Department of Chemical Engineering | |
curtin.accessStatus | Fulltext not available |
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