增强花状 SmMnOx 和 SmMnOx-rGO 催化剂的低温选择性催化还原 (SCR) 活性以及耐 H2O 和 SO2 性能

IF 3.4 3区 化学 Q2 CHEMISTRY, PHYSICAL Catalysis Communications Pub Date : 2024-02-01 DOI:10.1016/j.catcom.2024.106908
Yungang He , Sitong Meng , Haofeng Zhu , Kaijiao Duan , Yumei Duan , Jing Zhang , Lijuan Jia , Mingwu Xiang , Vishesh Manjunath , Ezhumalai David , Sivasankar Koppala
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引用次数: 0

摘要

采用共沉淀耦合溶热法成功合成了芦苇花状 SmMnO 和菜花状 SmMnO-rGO 催化剂,用于氮氧化物的选择性催化还原(SCR)。在 75-200 ℃ 的温度范围内,两种催化剂的氮氧化物转化率均超过 90%,SmMnO-rGO 的氮选择性超过 90%。此外,在 100 ℃ 的超低温下,这两种催化剂对 HO 和 SO 的抗性均超过 62%,远远优于共沉淀法制备的蓬松球状 SmMnO。此外,掺杂 rGO 后 Mn/Mn 的比例降低,阻碍了 NH 氧化的副反应,从而提高了掺杂 rGO 的 SmMnO 催化剂的 N 选择性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Enhanced low-temperature selective catalytic reduction (SCR) activity and H2O and SO2 resistance of flower-like SmMnOx and SmMnOx-rGO catalysts

Reed flower-like SmMnOx and cauliflower-like SmMnOx-rGO catalysts were successfully synthesized by a coprecipitation-coupled solvothermal method for selective catalytic reduction (SCR) of NOx. The NOx conversion of the two catalysts is more than 90% in the temperature range of 75–200 °C, and the N2 selectivity of SmMnOx-rGO is above 90%. Moreover, both of them exhibit more than 62% of resistance to H2O and SO2 at a very low temperature of 100 °C, much superior than the fluffy spherical SmMnOx prepared by coprecipitation method. The strong synergy between Mn and Sm endowed by the flower-like structure contributes to a low degree of crystallization, a high ratio of (Mn3++Mn4+)/Mn, more chemisorbed oxygen species, strong redox ability, and more Lewis acid sites, hence effectively enhancing low-temperature SCR activity and resistance to H2O and SO2. In addition, the decreased ratio of Mn4+/Mn after rGO doping hinders the side reaction of NH3 oxidation, thus enhancing the N2 selectivity of rGO-doped SmMnOx catalyst.

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来源期刊
Catalysis Communications
Catalysis Communications 化学-物理化学
CiteScore
6.20
自引率
2.70%
发文量
183
审稿时长
46 days
期刊介绍: Catalysis Communications aims to provide rapid publication of significant, novel, and timely research results homogeneous, heterogeneous, and enzymatic catalysis.
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