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Effect of samarium doping on the activity and sulfur resistance of Ce/MnFeO_(x) catalyst for low-temperature selective catalytic reduction of NO_(x) by ammonia    

文献类型:期刊文献

中文题名:Effect of samarium doping on the activity and sulfur resistance of Ce/MnFeO_(x) catalyst for low-temperature selective catalytic reduction of NO_(x) by ammonia

作者:Qiyao Zhang[1];Shuangshuang Zhang[1];Xu Hu[1];Yongmin Huang[1]

机构:[1]Key Laboratory of Specially Functional Polymeric Materials and Related Technology,School of Chemistry and Molecular Engineering,East China University of Science and Technology,Shanghai 200237,China

年份:2024

卷号:71

期号:7

起止页码:272

中文期刊名:Chinese Journal of Chemical Engineering

外文期刊名:中国化学工程学报(英文版)

收录:CSTPCD;;Scopus;CSCD:【CSCD2023_2024】;PubMed;

基金:supported by the Fundamental Research Funds for the Central Universities(222201817001);Shanghai Sailing Program(21YF140800).

语种:英文

中文关键词:SCR;Sm doping;Catalyst;Sulfur resistance;In situ DRIFTS;Selectivity

摘要:The self-made MnFeO_(x) catalysts doped with cerium and samarium were prepared by impregnation method for low-temperature selective catalytic reduction(SCR)by NH3.In this work,the surface properties of the series of MnFe-based catalysts were studied.The results indicate Sm-modified catalyst have superior low-temperature SCR activity;NO_(x) conversion maintained at nearby to 100%at 90℃ to 240℃.In addition,The N_(2) selectivity of Sm doping remains above 80%in the range of 60℃ to 150℃.In SO_(2) poisoning test,the NO_(x) conversion can be remained>90%after 10 h of reaction.The XPS,NH_(3)-TPD and H_(2)-TPR results show the catalyst with Sm doping enhances the acid sites and oxidation catalytic sites of mixed oxides serves for improving oxygen vacancies and transfer electrons.In situ diffuse reflaxions infrared Fourier transformations spectroscopy(DRIFTS)results show that NO_(x) is more easily adsorbed on the surface after Sm doping,which provided favorable conditions for the NH_(3)-SCR reaction to proceed.The reaction at the catalyst surface will follow the L-H reaction mechanism by transient reaction test.

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