2007
DOI: 10.1016/j.jcat.2006.09.012
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Redox features in the catalytic mechanism of the “standard” and “fast” NH3-SCR of NOx over a V-based catalyst investigated by dynamic methods

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Cited by 272 publications
(135 citation statements)
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“…In parallel, a fast decrease in the NO outlet concentration together with a mirror-like increment of the N 2 concentration, associated with the startup of the SCR reaction were observed. The levels of NH 3 , NO and N 2 at steady-state were in all cases consistent with the stoichiometry of the standard SCR reaction (2) [2,3,5,10,12,13,20,21]. Results obtained in the presence of different oxygen contents were qualitatively very similar.…”
Section: Transient Experiments Over the V-based Catalystsupporting
confidence: 74%
See 1 more Smart Citation
“…In parallel, a fast decrease in the NO outlet concentration together with a mirror-like increment of the N 2 concentration, associated with the startup of the SCR reaction were observed. The levels of NH 3 , NO and N 2 at steady-state were in all cases consistent with the stoichiometry of the standard SCR reaction (2) [2,3,5,10,12,13,20,21]. Results obtained in the presence of different oxygen contents were qualitatively very similar.…”
Section: Transient Experiments Over the V-based Catalystsupporting
confidence: 74%
“…The presented models implement kinetic schemes derived from an extensive investigation of reactivity, chemistry and catalytic mechanism of all the main SCR reactions over commercial V 2 O 5 -WO 3 /TiO 2 and Fe-zeolite catalysts performed in our laboratories during the last few years [2][3][4][5][6][7][8][9][10][11][12][13][14].The related rate expressions were fitted to transient data collected over powdered catalysts in the chemical regime, and in their global form allow the kinetic analysis of the full NH 3 -NO/NO 2 SCR reacting system.…”
Section: Introductionmentioning
confidence: 99%
“…A similar trend of desorption was observed for all of the catalysts, except the catalyst calcined at 700 C, where a higher calcination temperature resulted in a reduced production of the oxidizing material. When both NO and NO 2 were included into the feed, a fast SCR may have occurred when compared with the standard SCR of NO Koebel et al, 2002aKoebel et al, , 2002bTronconi et al, 2007). The oxidation activity tests for the conversion of NO to NO 2 by O 2 on the Mn/ TiO 2 catalysts prepared at different calcination temperatures were performed (Figure 7).…”
Section: No Oxidation Activitymentioning
confidence: 99%
“…Extensive research has been undertaken to understand the different aspects of standard V-based SCR catalysts. These efforts were aimed at revealing mechanistic details such as the nature of the active centers and the rate determining steps [10][11][12][13][14][15][16][17], the origin of catalyst aging [18] and the electronic interactions between the various catalyst components and the poisoning phenomena [19][20][21]. For this purpose, parameters such as the synthesis of the TiO2 support material [22,23], the synthesis method, the loading and the nature of WO3 and V2O5 and the structural change upon thermal/hydrothermal treatment have been addressed.…”
Section: Introductionmentioning
confidence: 99%