A Ce/hopcalite catalyst for low-temperature oxidation of CO:Preparation, performance and mechanism

被引:6
|
作者
Fan, Xiaohui [1 ]
Ma, Shihui [1 ]
Gan, Min [1 ]
Ji, Zhiyun [1 ]
Sun, Zengqing [1 ]
Liu, Lincheng [1 ]
机构
[1] Cent South Univ, Sch Minerals Proc & Bioengn, 932 South LushanRoad, Changsha 410083, Hunan, Peoples R China
基金
中国国家自然科学基金;
关键词
Hopcalite catalysts; Carbon monoxide; Surface modification; Low -temperature activity; Binding stability; MANGANESE OXIDE CATALYSTS; CARBON-MONOXIDE OXIDATION; CO OXIDATION; PREFERENTIAL OXIDATION; MIXED OXIDES; IONIC-CONDUCTIVITY; CUMNOX CATALYSTS; SURFACE-DEFECTS; EXCESS HYDROGEN; SOLID-SOLUTIONS;
D O I
10.1016/j.cej.2024.149636
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
The utilization of atomic-scale doping in catalysts has been recognized as an effective strategy for enhancing CO oxidation catalytic activity. This work adjusted the lattice structure of hopcalite (CuMnOx) catalysts via Cedoping. Ce species was uniformly dispersed on the surface of amorphous porous catalysts, which built abundant interfaces along with many active sites. The lattice distortion degree can be regulated by changing Ce dosage. The modified catalysts with 7.5 wt%Ce-doping exhibited the optimal intrinsic activity for CO oxidation. Compared with the original sample, the CO conversion increased by 50 % at room temperature, and the reaction rate was eight-fold faster, superior to most reported hopcalite catalysts. Integrating with the various characterizations, the enhancing of low-temperature activity mainly originates from the weakened binding of oxygen atoms by lattice distortions. Moreover, the experiments and characterization results revealed that the reactivity of both adsorbed and lattice oxygen is enhanced on Ce-modified samples at low temperature. This work provides new insights into the rational modulation of reactive oxygen species and reinforces the utility of hopcalite catalysts for oxidizing CO at low temperature.
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页数:14
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