Unveiling the effect of W and Co on PbO resistance over FeCe catalyst for low-temperature NH3-SCR of NO

被引:0
|
作者
She, Yuan [1 ,2 ]
Meng, Hao [1 ]
Shen, Zhenghua [1 ]
Niu, Wenkang [1 ]
Peng, Changqing [1 ]
Li, Kai [1 ]
Miao, Hongsheng [2 ]
Xing, Xiangdong [1 ]
Zhang, Zhaohui [1 ]
机构
[1] Xian Univ Architecture & Technol, Sch Met Engn, Xian 710055, Shaanxi, Peoples R China
[2] Xining Special Steel Co Ltd, Xining 810005, Peoples R China
关键词
Co-doping; PbO-resistance; FeCe catalyst; NH3-SCR reaction; REDUCTION; OXIDES; NH3; MN;
D O I
10.1016/j.jhazmat.2025.137221
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
The presence of PbO in the flue gas can poison FeCe catalyst, reducing its denitrification efficiency. In this work, the mechanism of PbO poisoning of FeCe catalyst, along with the effects of W and Co co-doping on the NO oxidation performance and PbO resistance of FeCe catalyst were investigated. The SBET of FeCe catalyst decreased and the crystallinity increased obviously after PbO poisoning. PbO could destroy the Bronsted acid sites and redox properties of FeCe catalyst. In addition, the conversion of NO to NO2 molecules and monodentate nitrites was also inhibited on FeCe catalyst. The NO conversion rate of the PWCo-FeCe catalyst reached 76 % at 220 degrees C, with larger SBET and lower degree of crystallization compared to PbO-FeCe catalyst. Besides, the codoping of W and Co facilitated the right shift of the Fe2 + + Ce4+ <-> Fe3+ + Ce3+ redox cycle, leading to a higher ratio of Fe3+ and Ce3+. Moreover, incorporation of W and Co boosted the number of Br & oslash;nsted acid sites and enhanced the formation of NO2 molecules and monodentate nitrite, which mitigated the suppressive effect of PbO on the NH3-SCR reaction. The FeCe and WCo-FeCe catalysts operated via E-R and L-H mechanisms, and PbO poisoning did not affect the established reaction pathways.
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页数:16
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