Low-Temperature Selective Catalytic Reduction of NO with NH3 over a Biochar-Supported Perovskite Oxide Catalyst

被引:8
|
作者
Fan, Xiaoxiong [1 ,2 ]
Hao, Lifang [1 ,2 ,3 ]
Gu, Xiangyu [1 ,4 ]
Li, Songgeng [1 ,2 ,3 ]
机构
[1] Chinese Acad Sci, Inst Proc Engn, State Key Lab Multiphase Complex Syst, Beijing 100190, Peoples R China
[2] Univ Chinese Acad Sci, Sino Danish Coll, Beijing 100049, Peoples R China
[3] Univ Chinese Acad Sci, Sch Chem Engn, Beijing 100049, Peoples R China
[4] Sino Danish Ctr Educ & Res, Beijing 100190, Peoples R China
关键词
MILD AIR OXIDATION; ACTIVATED CARBON; ENHANCED PERFORMANCE; NITROGEN-OXIDES; NH3-SCR; SCR; RESISTANCE; PYROLYSIS; MECHANISM; BIOMASS;
D O I
10.1021/acs.energyfuels.2c04291
中图分类号
TE [石油、天然气工业]; TK [能源与动力工程];
学科分类号
0807 ; 0820 ;
摘要
Maintaining high denitration efficiency for the selective catalytic reduction with ammonia (NH3-SCR) at low temperatures is challenging. In this work, a modified biochar-supported perovskite oxide catalyst was synthesized and implemented to NO conversion in the low temperature range of 100-250 degrees C. Different modification methods were compared, where the combination of nitric acid and air oxidation treatment endowed biochar with abundant acidic surface oxygen-containing groups and a higher specific surface area as a support. The perovskite oxide (LaMnO3) and the LaMnO3/biochar catalysts were prepared to investigate the interactions between the catalyst and the support. The LaMnO3/biochar catalyst exhibited excellent denitration efficiency and good N2 selectivity, achieving over 80% NO conversion within the entire temperature range of 100-250 degrees C (SN2 > 90%), and the highest NO conversion reached 95.8% at 225 degrees C (SN2 = 95.4%). This catalyst provided synergistic adsorption capacity for NH3 as a result of the acidic function of perovskite oxide and acidic oxygen-containing functional groups of the modified biochar support. Additionally, LaMnO3 showed an eminent redox capability for NO conversion due to the high content of Mn4+ and chemically adsorbed oxygen species. Finally, NH3-SCR reaction mechanisms were proposed on the basis of transient response experiments and in situ diffuse reflectance infrared Fourier transform spectra (DRIFTS) characterization.
引用
收藏
页码:7339 / 7352
页数:14
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