scholarly journals Selective Catalytic Reduction of NOx with Ammonia over Cu and Fe Promoted Zeolite Catalysts

2013 ◽  
Vol 19 (3) ◽  
pp. 287-294 ◽  
Author(s):  
Ho-Jung Ha ◽  
Ju-Hwan Hong ◽  
Joon-Hwan Choi ◽  
Jong-Dae Han
2019 ◽  
Author(s):  
Julian Rudolph ◽  
Christoph R. Jacob

<div> <div> <div> <p>We computationally investigate the mechanism of the reduction half-cycle of the selective catalytic reduction (SCR) of nitrogen oxides with ammonia. We compare both Fe- and Cu-doped zeolite catalysts and aim at exploring all accessible reaction pathways. From our calculations, a comprehensive picture emerges that unifies sev- eral previous mechanistic proposals. We find that both for Fe and for Cu catalysts, different reaction pathways are feasible, but some of the possible reaction pathways differ in these two cases. Our computational results provide a basis for the inter- pretation of in situ spectroscopic investigations that can possibly distinguish the different mechanistic pathways. </p> </div> </div> </div>


2014 ◽  
Vol 118 (19) ◽  
pp. 10204-10212 ◽  
Author(s):  
Dmitry E. Doronkin ◽  
Maria Casapu ◽  
Tobias Günter ◽  
Oliver Müller ◽  
Ronald Frahm ◽  
...  

2020 ◽  
Vol 44 (3) ◽  
pp. 817-831 ◽  
Author(s):  
Junqiang Xu ◽  
Yahua Qin ◽  
Honglin Wang ◽  
Fang Guo ◽  
Jiaqing Xie

This paper highlights the design strategies of the copper-based zeolite catalysts with excellent catalytic activity at low temperature for HC-SCR.


2018 ◽  
Vol 237 ◽  
pp. 263-272 ◽  
Author(s):  
Peirong Chen ◽  
Abhishek Khetan ◽  
Magdalena Jabłońska ◽  
Johannes Simböck ◽  
Martin Muhler ◽  
...  

2019 ◽  
Author(s):  
Julian Rudolph ◽  
Christoph R. Jacob

<div> <div> <div> <p>We computationally investigate the mechanism of the reduction half-cycle of the selective catalytic reduction (SCR) of nitrogen oxides with ammonia. We compare both Fe- and Cu-doped zeolite catalysts and aim at exploring all accessible reaction pathways. From our calculations, a comprehensive picture emerges that unifies sev- eral previous mechanistic proposals. We find that both for Fe and for Cu catalysts, different reaction pathways are feasible, but some of the possible reaction pathways differ in these two cases. Our computational results provide a basis for the inter- pretation of in situ spectroscopic investigations that can possibly distinguish the different mechanistic pathways. </p> </div> </div> </div>


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