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Insights into samarium doping effects on catalytic activity and SO2 tolerance of MnFeOx catalyst for low-temperature NH3-SCR reaction.

Authors :
Chen, Zhichao
Ren, Shan
Wang, Mingming
Yang, Jie
Chen, Lin
Liu, Weizao
Liu, Qingcai
Su, Buxin
Source :
Fuel. Aug2022, Vol. 321, pN.PAG-N.PAG. 1p.
Publication Year :
2022

Abstract

[Display omitted] • Sm-doping strengthened NH 3 -SCR activity and SO 2 tolerance over MnFeO x catalyst. • Enhanced NO 2 cooperated with increased NH 3 (ads) to cause "Fast SCR" reaction. • Sm induced Fe serving as sacrificial sites to preferentially react with SO 2. • Mechanism model for improving activity and SO 2 tolerance with Sm was proposed. The development of catalysts with high NH 3 -SCR activity in the presence of SO 2 was urgent for non-electric industries to control NO x emission at low temperature. Herein, a series of Sm-doping MnFeO x catalysts were synthesized through a typical PEG-assisted co-precipitation method and applied for low-temperature NH 3 -SCR process. SmMnFe-0.1 catalyst significantly broadened the activation temperature window and yielded almost 100% NO conversion from 75 to 200 °C, simultaneously, the NO removal efficiency still maintained at about 90% in the presence of SO 2 and H 2 O. The characterization results confirmed that Sm could optimize the dispersity of active components and enlarge the surface area of catalyst. Furthermore, strong interaction among active ions facilitated more oxygen vacancies and accelerated NO oxidizing to NO 2 , further cooperating with abundant adsorbed NH 3 , leading to cause "Fast SCR" reaction. Both catalysts were dominated by the E-R mechanism despite MnFeO x catalyst also obeyed the L-H pathway. Particularly, the intense redox circles between Sm and Mn inhibited the electron transferring from SO 2 to Mn ions, and induced Fe species serving as sacrificial sites along with Sm to preferentially react with SO 2 , resulting in an excellent SO 2 tolerance, and the possible mechanism model was proposed. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
00162361
Volume :
321
Database :
Academic Search Index
Journal :
Fuel
Publication Type :
Academic Journal
Accession number :
156913779
Full Text :
https://doi.org/10.1016/j.fuel.2022.124113