2009
DOI: 10.1016/j.apcatb.2009.09.028
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On the mechanism of the SCR reaction on Fe/HBEA zeolite

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Cited by 106 publications
(88 citation statements)
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“…In addition, Brandenberger et al 111 concluded that the Brønsted acid sites might not be required directly in the SCR process for adsorbing or activating NH 3 , but they were necessary to bind and disperse the reactive Fe 3+ ions in the preparation process for Fe-based zeolite catalysts, similar to the results reported by Iwasaki et al 104 Furthermore, the zeolite support with Brønsted acidity could also play a role as an NH 3 reservoir, regardless of the form in which the NH 3 was stored, and in the NH 3 -SCR reaction the stored NH 3 could migrate to the active sites so as to undergo a reaction with NO. 111 A similar spill-over effect of NH 3 on the zeolite support to the active Fe 3+ sites in the NH 3 -SCR reaction was also reported by Klukowski et al 112 on their Fe-HBEA catalyst. Therefore, in brief summary, nowadays researchers basically agree that in the standard NH 3 -SCR reaction the oxidation function of Fe-based zeolite catalysts and the amount of active Fe species, but not the acidic properties of the zeolite supports, are the main factors controlling the deNO x efficiency.…”
Section: Nh 3 -Scr Of No X Over Zeolite Catalystssupporting
confidence: 72%
“…In addition, Brandenberger et al 111 concluded that the Brønsted acid sites might not be required directly in the SCR process for adsorbing or activating NH 3 , but they were necessary to bind and disperse the reactive Fe 3+ ions in the preparation process for Fe-based zeolite catalysts, similar to the results reported by Iwasaki et al 104 Furthermore, the zeolite support with Brønsted acidity could also play a role as an NH 3 reservoir, regardless of the form in which the NH 3 was stored, and in the NH 3 -SCR reaction the stored NH 3 could migrate to the active sites so as to undergo a reaction with NO. 111 A similar spill-over effect of NH 3 on the zeolite support to the active Fe 3+ sites in the NH 3 -SCR reaction was also reported by Klukowski et al 112 on their Fe-HBEA catalyst. Therefore, in brief summary, nowadays researchers basically agree that in the standard NH 3 -SCR reaction the oxidation function of Fe-based zeolite catalysts and the amount of active Fe species, but not the acidic properties of the zeolite supports, are the main factors controlling the deNO x efficiency.…”
Section: Nh 3 -Scr Of No X Over Zeolite Catalystssupporting
confidence: 72%
“…Furthermore, the zeolite support with Brønsted acidity could play a role as NH 3 reservoir no matter what form of NH 3 was stored, and in the NH 3 -SCR reaction, the stored NH 3 could migrate to the active sites so as to undergo a reaction with NO [50]. A similar spillover effect of NH 3 on the zeolite support to the active Fe 3+ sites in the NH 3 -SCR reaction was also reported by Klukowski et al [51] on their Fe-HBEA catalyst.…”
Section: Acid Sites Of Fe-zeolite Catalysts In the Nh 3 -Scr Reactionsupporting
confidence: 56%
“…Recent in situ UV-vis and combined XAFS/XRD studies confirmed that such species remain intact during NH 3 -SCR and are thus responsible for the high catalytic activity [5,9]. A similar conclusion has recently been put forward for the high activity of Fe-BEA systems for the same reaction, the active species being proposed to be monomeric Fe 3+ species [10].…”
Section: Introductionmentioning
confidence: 77%