Catalysts Optimization of WO3‐SiO2 Supported Iridium for NOx Reduction by CO under Excess Oxygen Conditions

催化作用 氮氧化物 选择性催化还原 化学 氧气 X射线光电子能谱 无机化学 烟气 产量(工程) 材料科学 化学工程 物理化学 有机化学 冶金 工程类 燃烧
作者
Yuansong Zhou,Fengyu Gao,Xiaolong Tang,Jingxuan Meng,Ying Du,Honghong Yi
出处
期刊:ChemistrySelect [Wiley]
卷期号:7 (23) 被引量:6
标识
DOI:10.1002/slct.202104557
摘要

Abstract A series of Ir‐based catalysts were prepared by ultrasonic‐assisted equal‐volume impregnation to evaluate the catalytic performance of selective catalytic reduction of NOx by CO (CO‐SCR) with excess O 2 in simulated flue gas. We investigated the effects of different carrier, Ir loading, and composite carrier ratio (W/Si) on the CO‐SCR activities. The results showed that WO 3 and SiO 2 were effective carriers for the CO‐SCR reaction under oxygen‐rich conditions. Results of XRD and H 2 ‐TPR studies indicated that metal Ir strongly interacted with carrier WO 3 and SiO 2 , respectively, which improved the surface dispersion of active component Ir species and was conducive to the removal of NOx and CO. When W/Si molar ratio was 1/9 and Ir loading was 2 wt%, the Ir/WO 3 ‐SiO 2 catalyst reached 49 % NOx conversion and 76 % CO conversion at 225°C, while NO 2 yield was also only 5 ppm. The effects of O 2 , SO 2 , and H 2 O on the structure of Ir/WO 3 ‐SiO 2 were analyzed by XRD and XPS characterization methods. It was found that O 2 could oxidize Ir species to IrO 2 , thereby inhibiting NOx reduction. A low concentration of SO 2 can weaken the process of Ir oxidation, promote NOx reduction, and improve catalytic activity. H 2 O can reduce the NOx conversion rate and inhibit the CO‐SCR reaction, but the inhibition effect is reversible.
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