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dc.contributor.authorSun, W.
dc.contributor.authorLi, Xin Yong
dc.contributor.authorZhao, Q.
dc.contributor.authorTade, M.
dc.contributor.authorLiu, Shaomin
dc.date.accessioned2017-01-30T11:46:31Z
dc.date.available2017-01-30T11:46:31Z
dc.date.created2016-04-26T19:30:22Z
dc.date.issued2016
dc.identifier.citationSun, W. and Li, X.Y. and Zhao, Q. and Tade, M. and Liu, S. 2016. WaMn1 - aox Catalysts Synthesized by a One-Step Urea Co-precipitation Method for Selective Catalytic Reduction of NOx with NH3 at Low Temperatures. Energy and Fuels. 30 (3): pp. 1810-1814.
dc.identifier.urihttp://hdl.handle.net/20.500.11937/14862
dc.identifier.doi10.1021/acs.energyfuels.5b02252
dc.description.abstract

Selective catalytic reduction (SCR) of NOx with NH3 (NH3-SCR) at low temperatures is a promising technology for DeNOx (removal of NOx) as a result of its high NOx conversion, excellent selectivity, and broad application prospect. As a result of the remarkable activity under low temperature for SCR performance, Mn-based catalysts have attracted extensive attention. In this work, a series of WαMn1 – αOx (α = 0, 0.25, 0.33, 0.5, or 1) catalysts were synthesized by a one-step urea co-precipitation method and characterized by X-ray diffraction, Raman, X-ray photoelectron spectroscopy, thermogravimetric analysis, and scanning electron microscopy. Thereamong, the W0.33Mn0.66Ox catalyst showed the highest NH3-SCR activity within a broad temperature range of 230–470 °C. In addition, the active Mn and W species were in highly amorphous or poorly crystalline states. It was revealed that the interaction of W and Mn increased the chemistry oxygen content of the catalysts, thus enhancing the low-temperature SCR performance.

dc.publisherAmerican Chemical Society
dc.titleWaMn1 - aox Catalysts Synthesized by a One-Step Urea Co-precipitation Method for Selective Catalytic Reduction of NOx with NH3 at Low Temperatures
dc.typeJournal Article
dcterms.source.volume30
dcterms.source.number3
dcterms.source.startPage1810
dcterms.source.endPage1814
dcterms.source.issn0887-0624
dcterms.source.titleEnergy and Fuels
curtin.departmentDepartment of Chemical Engineering
curtin.accessStatusFulltext not available


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