催化作用
氮氧化物
吸附
无机化学
化学
氧化还原
硫黄
选择性催化还原
氧化物
分解
兴奋剂
硫酸盐
金属
材料科学
有机化学
光电子学
燃烧
作者
Hui Zhang,Zhihua Lian,Chunxi Lin,Ying Zhu,Wenpo Shan,Hong He
标识
DOI:10.1016/j.jcis.2023.08.129
摘要
Ceria-based catalysts for the selective catalytic reduction of NOx with NH3 (NH3-SCR) are always subject to deactivation by sulfur poisoning. In this study, Fe-doped Ce-W mixed oxides, which were synthesized by the co-precipitation method, improved the SCR activity and SO2 durability at low temperatures of undoped Ce-W oxides. The improved low-temperature activity was mainly due to the enhancement of redox properties at low temperatures and more active oxygen species, together with the adsorption and activation of more abundant NOx species, facilitating the “fast SCR” reaction. In the presence of SO2, doping with Fe species effectively prevented sulfate deposition on the CeW catalyst, due to the interaction between Fe, Ce, and W species inducing electron transfer among different metal sites and altering the electron distribution. The competitive adsorption behavior between NO and SO2 was changed by Fe doping, in which the adsorption and oxidation of SO2 were restrained. Besides, the elevated NO oxidation accelerated the decomposition of ammonium bisulfate, causing the SCR reaction to not be greatly suppressed. Hence, Fe-doped Ce-W oxides catalysts showed excellent sulfur resistance. This study helps provide an in-depth understanding of efficient Ce-based catalysts for SO2-tolerance strategies.
科研通智能强力驱动
Strongly Powered by AbleSci AI