Low-temperature NH3-SCR activity of M (M = Zr, Ni and Co) doped MnOx supported biochar catalysts

被引:69
作者
Chen, Lin [1 ,2 ]
Ren, Shan [1 ,2 ]
Liu, Weizao [1 ,2 ]
Yang, Jie [1 ,2 ]
Chen, Zhichao [1 ,2 ]
Wang, Mingming [1 ,2 ]
Liu, Qingcai [1 ,2 ]
机构
[1] Chongqing Univ, Coll Mat Sci & Engn, Chongqing 400044, Peoples R China
[2] Chongqing Univ, Chongqing Key Lab Vanadium Titanium Met & New Mat, Chongqing 400044, Peoples R China
来源
JOURNAL OF ENVIRONMENTAL CHEMICAL ENGINEERING | 2021年 / 9卷 / 06期
基金
中国国家自然科学基金;
关键词
MnOx catalysts; Low-temperature NH3-SCR; In situ DRIFTS; Langmuir-Hinshelwood (L-H) mechanism; HIGH SO2 TOLERANCE; MN/TIO2; CATALYST; ALKALI-METAL; REDUCTION; NH3; NO; SCR; CE; RESISTANCE; MECHANISM;
D O I
10.1016/j.jece.2021.106504
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
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.
引用
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页数:12
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