催化作用
路易斯酸
选择性催化还原
无机化学
氧化物
金属
生物炭
分解
氧化还原
化学
选择性
过渡金属
核化学
热解
有机化学
作者
Lin Chen,Shan Ren,Weizao Liu,Jie Yang,Zhichao Chen,Mingming Wang,Qingcai Liu
标识
DOI:10.1016/j.jece.2021.106504
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 oC and the best N2 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. Zr-Mn/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 (Oα), excellent redox property and more Lewis acid sites and Brønsted acid sites. From in situ DRIFTS, the Zr-Mn/BC catalyst followed Langmuir-Hinshelwood (L-H) reaction mechanism: the NH4+ species or NH3,ads reacted with the NxOy species (NO2,ads, NO2-, NO3-), finally generated N2 and H2O. In which the Zr doping could avoid the formation of N2O by restraining the decomposition of NH4NO3 intermediate.
科研通智能强力驱动
Strongly Powered by AbleSci AI