催化作用
选择性催化还原
烟气
空间速度
X射线光电子能谱
化学工程
化学
氧化物
氮氧化物
兴奋剂
傅里叶变换红外光谱
材料科学
无机化学
燃烧
物理化学
有机化学
选择性
光电子学
工程类
作者
Shilin Zhao,Junlin Peng,Yuxin Qian,Zhiqiang Sun
标识
DOI:10.1016/j.fuproc.2023.107704
摘要
Low-temperature deNOx selective catalytic reduction (SCR) catalysts are of great significance to prolong catalyst life and reduce flue gas temperature. In this work, the low-temperature deNOx performance of different zFeCexMny catalysts was investigated on a simulated flue gas fixed-bed experimental bench. BET, XRD, XPS, NH3-TPD, and in situ FT-IR were used to characterize the physical-chemical properties of the samples. The optimum ratio and deNOx mechanism of the catalysts were explored. The results show 4FeMn7Ce3 doped with 4 wt% Fe based on Mn7Ce3 has the best deNOx performance. Its deNOx efficiency is over 90% at 120–220 °C and GHSV = 50,000 h−1, with the peak value of 98% at 150 °C. The Fe doping makes the oxide distributed uniformly on the catalyst's surface, promotes the valence cycle of the catalyst, yields more Mn4+ and Ce3+ species, and prompts the optimal deNOx temperature to the low temperature direction. Meanwhile, Lewis acid sites on the catalyst's surface are enhanced, which can promote the amide species formation that is beneficial for the deNOx reaction. Combined with in situ FTIR, the E-R mechanism and the L-H mechanism coexist in the deNOx process of zFeCexMny catalysts. These findings are helpful for the development of high-performance low-temperature deNOx catalysts.
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