Kiwi twig biochar recycling promoting the reduction of NO by a MnO2 catalyst

被引:9
作者
Fan, Hao [1 ,2 ]
Shen, Zhenxing [1 ,2 ]
Wang, Xiuru [1 ]
Fan, Jie [1 ]
Sun, Jian [1 ]
Chang, Tian [3 ]
Huang, Yu [2 ]
Wang, Xin [4 ]
Sun, Jiaxiang [5 ]
机构
[1] Xi An Jiao Tong Univ, Dept Environm Sci & Engn, Xian Key Lab Solid Waste Recycling & Resource Rec, Xian 710049, Peoples R China
[2] Chinese Acad Sci, Inst Earth Environm, State Key Lab Loess & Quaternary Geol, Xian 710049, Peoples R China
[3] Shaanxi Univ Sci & Technol, Sch Environm Sci & Engn, Xian 710021, Peoples R China
[4] Georgia Inst Technol, Sch Chem & Biomol Engn, Atlanta, GA 30332 USA
[5] Xi An Jiao Tong Univ, Instrumental Anal Ctr, Xian 710049, Peoples R China
关键词
Kiwi twigs; Oxygen vacancy; Selective catalytic reaction; Reaction mechanism; High value utilization; LOW-TEMPERATURE NH3-SCR; SCR; NH3; CE; NANOTUBES; OXIDATION; GRAPHENE; TITANIA; OXIDES; CARBON;
D O I
10.1016/j.apsusc.2022.153644
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Kiwi twigs have abundant vessels and sieve tubes, which may provide abundant nanotube structures and active sites. In this study, kiwi twig biochar was used to modify the alpha-manganese dioxide (MnO2) catalyst through facile potassium hydroxide solution (KOH) activation to improve N-2 selectivity in selective catalytic reduction (SCR). Results suggested that the C10.5MnO2 catalyst exhibited higher NO conversion (approximately 90%) and N-2 selectivity (> 95%) at 100 ?C-250 ?C. Moreover, biochar C1, which was directly mixed with KOH, increased the number of acid sites and lattice defects in the C10.5MnO2 catalyst; thus, the redox and acid cycles more easily occurred on the surface of the C10.5MnO2 catalyst than on that of the C(20.5)MnO2 catalyst. Moreover, the SCR process of the modified catalysts involved both Langmuir-Hinshelwood and Eley-Rideal mechanisms. This study demonstrated the effect of biochar on reaction sites and processes, providing a new perspective for the application of biochar in the field of catalysis.
引用
收藏
页数:9
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