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Ordered Mesoporous MnAlOx Oxides Dominated by Calcination Temperature for the Selective Catalytic Reduction of NOx with NH3 at Low Temperature
被引:4
|作者:
Hou, Qixiong
[1
]
Liu, Yongjin
[1
,2
]
Hou, Yaqin
[1
]
Han, Xiaojin
[1
]
Huang, Zhanggen
[1
,2
]
机构:
[1] Chinese Acad Sci, Inst Coal Chem, State Key Lab Coal Convers, Taiyuan 030001, Peoples R China
[2] Univ Chinese Acad Sci, Beijing 100049, Peoples R China
来源:
基金:
中国国家自然科学基金;
关键词:
ordered mesoporous MnAlOx;
calcination temperature;
SCR;
low temperature;
CARBON NANOTUBES;
SUPPORTED MANGANESE;
SPINEL PERFORMANCE;
EFFICIENT CATALYST;
METAL;
SCR;
MN;
FE;
MECHANISM;
ADSORPTION;
D O I:
10.3390/catal12060637
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:
Manganese alumina composited oxides (MnAlOx) catalysts with ordered mesoporous structure prepared by evaporation-induced self-assembly (EISA) method was designed for the selective catalytic reduction (SCR) of NOx with NH3 at low temperature. The effect of calcination temperature of MnAlOx catalysts was investigated systematically, and it was correlated with SCR activity. Results showed that with an increase in calcination temperature, the SCR activity of MnAlOx catalysts increased. When the calcination temperature was raised up to 800 degrees C, the NOx conversion was more than 90% in the operation temperature range of 150 similar to 240 degrees C. Through various characterization analysis, it was found that MnAlOx-800 degrees C catalysts possessed enhanced redox capacities as the higher content of Mn4+/(Mn3+ + Mn4+). Moreover, the improved redox properties could contribute to a higher NOx adsorption and activation ability, which lead to higher SCR performance of MnAlOx-800 degrees C catalysts. In situ DRIFTs revealed that the adsorbed NO2 and bidentate nitrate are the reactive intermediate species, and NH3 species bonded to Lewis acid sites taken part in SCR progress. The SCR progress predominantly followed E-R mechanism, while L-H mechanism also takes effect to a certain degree.
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页数:18
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