Insight into the promotional effect of Mn-modified nitrogenous biochar on the NH3-SCR denitrification activity at low temperatures

被引:17
作者
Feng, Xiangdong [1 ]
Liu, Shanjian [1 ,2 ]
Yue, Kang [1 ]
Wei, Heng [1 ]
Bi, Dongmei [1 ,2 ]
Zhao, Wenjing [1 ]
机构
[1] Shandong Univ Technol, Sch Agr Engn & Food Sci, Zibo 255000, Peoples R China
[2] State Key Lab Woody Oil Resources Utilizat, Zibo 255000, Peoples R China
基金
中国国家自然科学基金;
关键词
Mn doping; Cotton straw biochar; Surface chemistry; Reaction mechanisms; NH3-SCR; SELECTIVE CATALYTIC-REDUCTION; N-DOPED GRAPHENE; ACTIVATED CARBON; SO2; TOLERANCE; NITRIC-OXIDE; NH3; MECHANISM; SCR; NOX; ADSORPTION;
D O I
10.1016/j.energy.2023.129323
中图分类号
O414.1 [热力学];
学科分类号
摘要
A series of Mn-doped nitrided cotton straw biochar catalysts were prepared, and the effect of Mn doping on the denitrification activity at low temperatures was investigated. The microstructure and surface chemistry of the catalyst were studied. The results showed that the low-temperature denitrification activity of the Mn-doped nitride cotton straw biochar was significantly improved, and the optimal reactivity temperature was broadened. The catalyst with 6 wt% Mn/NCAC-1.5-7 (Mn(6)/NCAC-1.5-7) removed 100 % of NO in the temperature range of 140-200 degrees C, and the N2 selectivity is close to 100 % throughout the reaction temperature interval of 50-260 degrees C. The presence of many different Bronsted and Lewis acid sites on the catalyst enhanced its NH3 adsorption capacity. The monodentate nitrite produced by Mn doping could be reduced by NH3 at low temperatures, which may be why the doping of Mn improved the low-temperature denitrification activity of the catalyst. In addition, an Eley-Rideal (E-R) mechanism existed for the reaction of adsorbed NH3 linked to Lewis acid sites with gaseous NO over Mn-modified nitrided cotton straw biochar catalysts. There was also a LangmuirHinshelwood (L-H) mechanism between the adsorbed NH3 and adsorbed NO states. The E-R mechanism dominated the low temperature NH3-SCR reaction.
引用
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页数:13
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