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Ultra hydrothermal stability of CeO2-WO3/TiO2 for NH3-SCR of NO compared to traditional V2O5-WO3/TiO2 catalyst

Paper ID Volume ID Publish Year Pages File Format Full-Text
53879 46988 2015 6 PDF Available
Title
Ultra hydrothermal stability of CeO2-WO3/TiO2 for NH3-SCR of NO compared to traditional V2O5-WO3/TiO2 catalyst
Abstract

•Compared Ce-W/Ti and commercial V-W/Ti catalyst.•The novel Ce-W/Ti catalyst exhibited much better resistance to hydrothermal aging at 670 °C in 5% H2O/air for 64 h.•CeO2 inhibit TiO2 sintering and TiO2 phase transition from anatase to rutile.•Reducibility and surface acidity are studied by TPR and In-situ DRIFTS spectra methods.

To meet stringent emission standard above European VI, the hydrothermal stability of NH3-SCR catalyst is very important for removal of NOx from diesel engines. In this work, V2O5-WO3/TiO2 (denotes as V-W/Ti) and CeO2-WO3/TiO2 (denotes as Ce-W/Ti) catalysts were prepared by impregnation method. The NH3-SCR activity of fresh and hydrothermal aged catalysts was studied. Comparing with traditional V-W/Ti catalyst, the novel Ce-W/Ti catalyst exhibited much better resistance to hydrothermal aging. More than 80% of NO conversion was obtained over Ce-W/Ti catalyst in the temperature range of 238–573 °C even after hydrothermal treatment at 670 °C in 5% H2O/air for 64 h. The characterization results revealed that the existence of Ce4+-Ce3+ couple contribute to provide more oxygen vacancies and improve the surface Lewis acid of catalyst and affect the surface adsorbed NH3 species. CeO2 could inhibit the segregation and crystallization of WOx species due to the solid state reactions (Ce2(WO4)3) provided more Brønsted acid sites (W-O-W or WO modes of Ce2(WO4)3). In addition, CeO2 inhibit the sintering or phase transition of anatase TiO2 and make the catalyst keep the high surface area, which was favorable to keep more acid sites.

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Keywords
DeNOx; NH3-SCR; V2O5-WO3/TiO2; CeO2-WO3/TiO2; Hydrothermal Stability.
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Ultra hydrothermal stability of CeO2-WO3/TiO2 for NH3-SCR of NO compared to traditional V2O5-WO3/TiO2 catalyst
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Publisher
Database: Elsevier - ScienceDirect
Journal: Catalysis Today - Volume 258, Part 1, 1 December 2015, Pages 11–16
Authors
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Subjects
Physical Sciences and Engineering Chemical Engineering Catalysis
Get Full-Text Now
Don't Miss Today's Special Offer
Price was $35.95
You save - $31
Price after discount Only $4.95
100% Money Back Guarantee
Full-text PDF Download
Online Support
Any Questions? feel free to contact us