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dc.contributor.authorLiu, J.
dc.contributor.authorLiu, Jian
dc.contributor.authorZhao, Z.
dc.contributor.authorWei, Y.
dc.contributor.authorSong, W.
dc.date.accessioned2017-07-27T05:20:17Z
dc.date.available2017-07-27T05:20:17Z
dc.date.created2017-07-26T11:11:18Z
dc.date.issued2017
dc.identifier.citationLiu, J. and Liu, J. and Zhao, Z. and Wei, Y. and Song, W. 2017. Fe-Beta@CeO2 core-shell catalyst with tunable shell thickness for selective catalytic reduction of NOx with NH3. AI Ch E Journal. 63 (10): pp. 4430–4441.
dc.identifier.urihttp://hdl.handle.net/20.500.11937/54266
dc.identifier.doi10.1002/aic.15743
dc.description.abstract

A series of core-shell structural deNO x catalysts using small-grain Beta supporting FeO x nanoparticles as the core and tunable CeO 2 thin film thickness as sheaths were designed and controllably synthesized. Their catalytic performances were tested for selective catalytic reduction of NO x with NH 3 (NH 3 -SCR). It was found that CeO 2 shell thickness plays an important role in influencing the acidity and redox properties of the catalysts. Fe-Beta at CeO 2 core-shell catalysts exhibit excellent resistance to H 2 O and SO 2 and high NO x conversion (above 90%) in the wide temperature range (225-565°C). The kinetics result indicates that the coating of CeO 2 shell significantly increases the pore diffusion resistance of Fe-Beta at CeO 2 catalysts. Furthermore, in situ DRIFT results reveal that CeO 2 shell can promote the formation of NO 2 and cis- N2O2- species. But too thick CeO 2 shell (~20 nm) would result in the formation of inactive nitrate species, and thereby lead to a decrease of high-temperature activity of the catalysts.

dc.publisherJohn Wiley & Sons, Inc.
dc.titleFe-Beta@CeO2 core-shell catalyst with tunable shell thickness for selective catalytic reduction of NOx with NH3
dc.typeJournal Article
dcterms.source.issn0001-1541
dcterms.source.titleAI Ch E Journal
curtin.departmentDepartment of Chemical Engineering
curtin.accessStatusOpen access via publisher


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