期刊
CHINESE JOURNAL OF CHEMICAL ENGINEERING
卷 50, 期 -, 页码 301-309出版社
CHEMICAL INDUSTRY PRESS CO LTD
DOI: 10.1016/j.cjche.2022.05.028
关键词
NH3-SCR; NbCe catalyst; Cu modification; NO2 promoting effect; Fast-SCR; Flue gas
资金
- National Natural Science Foundation of China, China [21972062, 21976081, 21976111]
A simple Cu modification strategy was proposed to broaden the operation temperature window of NbCe catalyst. The study revealed that Cu modification significantly enhanced the activity and resistance of the catalyst, improving the efficiency of the NH3-SCR reaction through enhanced redox behavior and additional adsorption and activation sites.
A simple strategy of Cu modification was proposed to broaden the operation temperature window for NbCe catalyst. The best catalyst Cu-0.010/Nb1Ce3 presented over 90% NO conversion in a wide temperature range of 200-400 degrees C and exhibited an excellent H2O or/and SO2 resistance at 275 degrees C. To understand the promotional mechanism of Cu modification, the correlation among the activity-structure-property were tried to establish systematically. Cu species highly dispersed on NbCe catalyst to serve as the active component. The strong interaction among Cu, Nb and Ce promoted the emergence of NbO4 and induced more Bronsted acid sites. And Cu modification obviously enhanced the redox behavior of the NbCe catalyst. Besides, EPR probed the Cu species exited in the form of monomeric and dimeric Cu2+, the isolated Cu2+ acted as catalytic active sites to promote the reaction: Cu2+-NO3-+NO(g) -> Cu2+-NO2-+NO2(g). Then the generated NO2 would accelerate the fast-SCR reaction process and thus facilitated the low-temperature deNO(x) efficiency. Moreover, surface nitrates became unstable and easy to decompose after Cu modification, thus providing additional adsorption and activation sites for NH3, and ensuring the improvement of catalytic activity at high temperature. Since the NH3-SCR reaction followed by E-R reaction pathway efficaciously over Cu-0.010/Nb1Ce3 catalyst, the excellent H2O and SO2 resistance was as expected. (C) 2022 The Chemical Industry and Engineering Society of China, and Chemical Industry Press Co., Ltd. All rights reserved.
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