The Enhancement of CO Oxidation Performance and Stability in SO2 and H2S Environment on Pd-Au/FeOX/Al2O3 Catalysts

被引:3
|
作者
He, Qingrong [1 ,2 ]
Wang, Xuwei [2 ]
Liu, Yimeng [1 ,2 ]
Kong, Weimin [2 ]
Ren, Shanshan [2 ]
Liang, Yun [1 ]
Tang, Min [1 ]
Zhou, Shuyuan [1 ,2 ]
Dong, Yanchun [2 ]
机构
[1] South China Univ Technol, Sch Light Ind & Engn, Guangzhou 510640, Peoples R China
[2] State Key Lab NBC Protect Civilian, Beijing 100083, Peoples R China
基金
中国国家自然科学基金;
关键词
Pd-Au; SO2; H2S; CO oxidation; Au/FeOx/Al2O3; PD; NANOPARTICLES; METHANE; PRECIPITATION; ADSORPTION; CONVERSION;
D O I
10.3390/ma16103755
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
Carbon monoxide (CO) is a colourless, odourless, and toxic gas. Long-term exposure to high concentrations of CO causes poisoning and even death; therefore, CO removal is particularly important. Current research has focused on the efficient and rapid removal of CO via low-temperature (ambient) catalytic oxidation. Gold nanoparticles are widely used catalysts for the high-efficiency removal of high concentrations of CO at ambient temperature. However, easy poisoning and inactivation due to the presence of SO2 and H2S affect its activity and practical application. In this study, a bimetallic catalyst, Pd-Au/FeOx/Al2O3, with a Au:Pd ratio of 2:1 (wt%) was formed by adding Pd nanoparticles to a highly active Au/FeOx/Al2O3 catalyst. Its analysis and characterisation proved that it has improved catalytic activity for CO oxidation and excellent stability. A total conversion of 2500 ppm of CO at 30 degrees C was achieved. Furthermore, at ambient temperature and a volume space velocity of 13,000 h(-1), 20,000 ppm CO was fully converted and maintained for 132 min. Density functional theory (DFT) calculations and in situ FTIR analysis revealed that PdAu/FeOx/Al2O3 exhibited stronger resistance to SO2 and H2S adsorption than the Au/FeOx/Al2O3 catalyst. This study provides a reference for the practical application of a CO catalyst with high performance and high environmental stability.
引用
收藏
页数:17
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