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The positive role of Ir0 and OV on the reduction of SO2 by CO over Ir/CeO2
被引:9
作者:

Cao, Jinyan
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Kunming Univ Sci & Technol, Fac Environm Sci & Engn, Kunming 650500, Peoples R China
Kunming Univ Sci & Technol, Natl Reg Engn Ctr Recovery Waste Gases Met & Chem, Kunming 650500, Peoples R China Kunming Univ Sci & Technol, Fac Environm Sci & Engn, Kunming 650500, Peoples R China

Lin, Yutao
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Kunming Univ Sci & Technol, Fac Environm Sci & Engn, Kunming 650500, Peoples R China Kunming Univ Sci & Technol, Fac Environm Sci & Engn, Kunming 650500, Peoples R China

Shao, Tianrun
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Kunming Univ Sci & Technol, Fac Environm Sci & Engn, Kunming 650500, Peoples R China Kunming Univ Sci & Technol, Fac Environm Sci & Engn, Kunming 650500, Peoples R China

Zhang, Qiulin
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Kunming Univ Sci & Technol, Fac Environm Sci & Engn, Kunming 650500, Peoples R China
Kunming Univ Sci & Technol, Natl Reg Engn Ctr Recovery Waste Gases Met & Chem, Kunming 650500, Peoples R China Kunming Univ Sci & Technol, Fac Environm Sci & Engn, Kunming 650500, Peoples R China

Ning, Ping
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Kunming Univ Sci & Technol, Fac Environm Sci & Engn, Kunming 650500, Peoples R China
Kunming Univ Sci & Technol, Natl Reg Engn Ctr Recovery Waste Gases Met & Chem, Kunming 650500, Peoples R China Kunming Univ Sci & Technol, Fac Environm Sci & Engn, Kunming 650500, Peoples R China

Chen, Jianjun
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Kunming Univ Sci & Technol, Fac Environm Sci & Engn, Kunming 650500, Peoples R China
Kunming Univ Sci & Technol, Natl Reg Engn Ctr Recovery Waste Gases Met & Chem, Kunming 650500, Peoples R China Kunming Univ Sci & Technol, Fac Environm Sci & Engn, Kunming 650500, Peoples R China

Tian, Guocai
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机构:
Kunming Univ Sci & Technol, Fac Met & Energy Engn, Kunming 650093, Peoples R China Kunming Univ Sci & Technol, Fac Environm Sci & Engn, Kunming 650500, Peoples R China

Yin, Liangtao
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机构:
Kunming Univ Sci & Technol, Fac Environm Sci & Engn, Kunming 650500, Peoples R China Kunming Univ Sci & Technol, Fac Environm Sci & Engn, Kunming 650500, Peoples R China

Xu, Siyuan
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Kunming Univ Sci & Technol, Fac Environm Sci & Engn, Kunming 650500, Peoples R China Kunming Univ Sci & Technol, Fac Environm Sci & Engn, Kunming 650500, Peoples R China

Nie, Rongbing
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h-index: 0
机构:
Kunming Univ Sci & Technol, Fac Environm Sci & Engn, Kunming 650500, Peoples R China Kunming Univ Sci & Technol, Fac Environm Sci & Engn, Kunming 650500, Peoples R China
机构:
[1] Kunming Univ Sci & Technol, Fac Environm Sci & Engn, Kunming 650500, Peoples R China
[2] Kunming Univ Sci & Technol, Natl Reg Engn Ctr Recovery Waste Gases Met & Chem, Kunming 650500, Peoples R China
[3] Kunming Univ Sci & Technol, Fac Met & Energy Engn, Kunming 650093, Peoples R China
基金:
中国国家自然科学基金;
关键词:
Elemental sulfur;
Ir;
CeO;
2;
catalyst;
Preparation variable;
Catalytic reduction;
Redox mechanism;
CATALYTIC-REDUCTION;
NO REDUCTION;
SELECTIVE REDUCTION;
CRYSTAL-PLANE;
CERIA;
PERFORMANCE;
MORPHOLOGY;
PD/CEO2;
O-2;
NANOPARTICLES;
D O I:
10.1016/j.apsusc.2023.156826
中图分类号:
O64 [物理化学(理论化学)、化学物理学];
学科分类号:
070304 ;
081704 ;
摘要:
Several Ir/CeO2 catalysts were synthesized with different preparation variable, the variable influences the SO2 reduction by CO over Ir/CeO2 catalyst through changing the specific surface area, the content of Ir0 species and the concentration of oxygen vacancies on the surface of catalysts. The characteristic results showed that the asprepared Ir/CeO2-6 catalyst has the highest crystallinity, the smallest grain size and the largest lattice parameter among the synthesized catalysts. All these three catalysts are mesoporous structures, and Ir/CeO2-6 has the largest pore size and specific surface area. DFT results showed that the adsorption energies of CO and SO2 at higher Ir loading is consistent with the stoichiometric ratio. Combining the results of Raman, XPS and H2-TPR, Ir/CeO2-6 has the highest Ce3+ content, OVs content and Ir0 content which exhibited the strongest Ir-O-Ce interaction and caused better catalytic activity. All the as-prepared catalysts follow the redox mechanism during reactions. This study illustrates the preparation method affecting microstructure and then the reaction activity, providing research ideas for modulating the preparation of efficient CeO2-based catalyst for SO2 reduction by CO.
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页数:10
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