Boosting NO removal performance of selective catalytic reduction with NH3 on hydrotalcite derived NiCuFe mixed oxides synthesized via urea hydrothermal method

被引:1
|
作者
Yang, Fan [1 ]
Wang, Xinpeng [1 ]
Qu, Chao [1 ]
Meng, Fanwei [1 ]
Liu, Wenyi [1 ]
Ye, Qing [1 ]
机构
[1] Beijing Univ Technol, Coll Environm & Energy Engn, Dept Environm Sci, Key Lab Beijing Reg Air Pollut Control, Beijing 100124, Peoples R China
基金
中国国家自然科学基金;
关键词
NH3-SCR; NiCuFeOx; LDO; Heterogeneous catalysis; Urea Hydrothermal; ENHANCED NH3-SCR; SCR; CE; OXIDATION; ACIDITY; REDOX; DRIFT; FE; CU;
D O I
10.1007/s11144-024-02590-5
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
NiCuFe layered double oxide (LDO) catalysts were synthesized using co-precipitation, impregnation, and urea hydrothermal methods. The NH3-SCR activity of NiCuFe-LDO catalysts was investigated to determine the effect of different synthesis methods. All NiCuFe-LDO samples exhibited good catalytic performance at low temperatures, with the sample synthesized using the urea hydrothermal method (NiCuFe-LDO-3) being the most efficient catalyst. The NiCuFe-LDO-3 catalyst achieved over 80% NO conversion in the temperature range of 180(degrees)C to 280 C-degrees, with a peak of 95.13% at 240(degrees)C. The physicochemical properties of the samples were systematically characterized using XRD, SEM, BET, NH3-TPD, H-2-TPR, XPS, and in-situ DRIFTS. The results showed that the NiCuFe-LDO-3 sample had the best crystallinity, as demonstrated by XRD and SEM. BET analysis revealed that the NiCuFe-LDO-3 sample had the largest specific surface area. The NiCuFe-LDO-3 sample was found to have more acidic sites and a better redox capacity than the other samples, according to the H-2-TPR and NH3-TPD results. In-situ DRIFTS analysis showed that the catalyst operates through both E-R and L-H reaction mechanisms.
引用
收藏
页码:1435 / 1454
页数:20
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