Simultaneous improvement of ammonia mediated NOx SCR and soot oxidation for enhanced SCR-on-Filter application

被引:22
作者
Martinovic, Ferenc [1 ]
Andana, Tahrizi [1 ]
Piumetti, Marco [1 ]
Armandi, Marco [1 ,2 ]
Bonelli, Barbara [1 ,2 ]
Deorsola, Fabio Alessandro [1 ]
Bensaid, Samir [1 ]
Pirone, Raffaele [1 ]
机构
[1] Politecn Torino, Dept Appl Sci & Technol, Corso Duca Abruzzi 24, I-10129 Turin, Italy
[2] Torino Politecn, INSTM Unit, Corso Duca Abruzzi 24, I-10129 Turin, Italy
关键词
SCR on filter; Soot oxidation; SCR; Fe-ZSM-5; Cu-ZSM-5; SELECTIVE CATALYTIC-REDUCTION; HYBRID CATALYSTS; NITROGEN-OXIDES; DIESEL; PERFORMANCE; COMBUSTION; EMISSIONS; POTASSIUM; COMPONENT; AG/AL2O3;
D O I
10.1016/j.apcata.2020.117538
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The integration of NOx reduction and catalytic soot oxidation was investigated for the SCRoF (Selective Catalytic Reduction on Filter) applications. By physically mixing a commercial SCR catalyst (either Fe-ZSM-5 and Cu-ZSM-5) with a soot oxidation catalyst (K/CeO2-PrO2), it was possible to lower the soot oxidation temperature by more than 150 degrees and, by optimizing the catalysts mass ratio in the mixture, NOx conversion simultaneously increased, because NO oxidation induced a fast SCR reaction pathway, unlike during standard SCR. Such an improvement in NOx conversion was more pronounced with the Fe-ZSM-5 than with the Cu-ZSM-5 zeolite, as the latter was more sensitive to the NO2/NOx ratio. In order to make the soot oxidation catalyst inactive towards ammonia oxidation, poisoning of the surface acid sites with 3.0 wt% K2CO3 (corresponding to only 1.0 wt.% K) was performed. In the soot oxidation and SCR catalysts physical mixture, the soot was oxidized mainly by O-2 and the contribution of NO2 to oxidation was negligible, as NO2 itself was a key reactant in the (kinetically much faster) SCR reaction.
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页数:10
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