Journal
JOURNAL OF ENVIRONMENTAL CHEMICAL ENGINEERING
Volume 9, Issue 6, Pages -Publisher
ELSEVIER SCI LTD
DOI: 10.1016/j.jece.2021.106504
Keywords
MnOx catalysts; Low-temperature NH3-SCR; In situ DRIFTS; Langmuir-Hinshelwood (L-H) mechanism
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Funding
- National Natural Science Foundation of China [52174298, 51874058]
- Graduate Research and Innovation Foundation of Chongqing [CYB21002]
- Chongqing Talents Plan for Young Talents [CQYC201905017]
- Chongqing Human Resources and Social Security Bureau [cx2020028]
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By doping different metal oxides and studying their effects on the low-temperature SCR activity of catalysts, it was found that the Zr-Mn/BC catalyst exhibited the best performance, including higher NO conversion rate and better resistance. Furthermore, Zr doping also influenced the reaction mechanism of the catalysts.
Several metal (Zr, Ni and Co) oxides doped biochar (BC) supported Mn oxide (MnOx) catalysts were prepared by impregnation method, and their effects on the low-temperature selective catalytic reduction with NH3(LT NH3-SCR) activity were studied. Zr-Mn/BC catalyst exhibited the highest NO conversion of around 87% at 200 degrees C and the best N-2 selectivity of the four catalysts. Furthermore, Zr-Mn/BC catalyst showed better resistance of SO2 and H2O than that of Mn/BC catalyst. Metal oxides were evenly distributed on the surface of the four catalysts. ZrMn/BC catalyst, Ni-Mn/BC catalyst and Co-Mn/BC catalyst had lower surface area compared with Mn/BC catalyst. Moreover, the high activity of Zr-Mn/BC catalyst was related to its higher concentration of Mn4+, more surface oxygen (O-alpha), excellent redox property and more Lewis acid sites and Bronsted acid sites. From in situ DRIFTS, the Zr-Mn/BC catalyst followed Langmuir-Hinshelwood (L-H) reaction mechanism: the NH4+ species or NH3ads reacted with the NxOy species (NO2,ads, NO2-, NO3-), finally generated N-2 and H2O. In which the Zr doping could avoid the formation of N2O by restraining the decomposition of NH4NO3 intermediate.
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