氮氧化物
催化作用
碱金属
选择性催化还原
化学
吸附
兴奋剂
钴
无机化学
材料科学
有机化学
光电子学
燃烧
作者
Xin Zhe Lan,Yilun Jing,Ruixia Xu,Ling Zhao,Haigang Hao
标识
DOI:10.1016/j.jece.2023.110251
摘要
It is undeniable that catalyst poisoning and deactivation ascribed to alkali metals in exhaust gas is still a thorny matter in selective catalytic reduction of NOx. Herein, under the premise of maintaining the excellent activity of CuCoAlO, Ce doping validly boosts the 3 wt% K resistance of the catalyst, the NOx conversion rate reaches 91% at 250 °C, which is 60% higher than the unmodified K poisoning catalyst. By tracking the evolution of reaction intermediates and combining the theoretical calculation, it was found that the reduced cumulative coverage of stable nitrate species is the main reason for the enhanced alkali resistance. Notably, the introduction of Ce efficiently preserves the reducibility and provides a considerable amount of surface adsorbed oxygen, which accelerates the activation of CO and NO and further benefits the CO-SCR. Hoping this work will provide an inspiration for the design of SCR catalysts with more reliable and distinguished alkaline resistance.
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