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Vanadium catalyst based on a tungsten trioxide structure modified with antimony in NH3-selective catalytic reduction for improved low-temperature activity
被引:16
作者:
Shin, JungHun
[1
]
Choi, GyeongRyun
[1
]
Hong, SungChang
[2
]
机构:
[1] Kyonggi Univ, Grad Sch, Dept Environm Energy Engn, 94-6 San, Suwon 443760, Gyeonggi Do, South Korea
[2] Kyonggi Univ, Dept Environm Energy Engn, 94-6 San, Suwon 443760, Gyeonggi Do, South Korea
关键词:
Antimony;
NH3-selective catalytic reduction;
Diffuse reflectance infrared Fourier transform spectroscopy Vanadium;
Reaction route;
Ammonia;
FAST SCR REACTION;
V2O5/TIO2;
CATALYST;
NH3-SCR ACTIVITY;
DOPED MN/TIO2;
FE-ZEOLITE;
NOX;
PERFORMANCE;
NH3;
OXIDE;
CERIA;
D O I:
10.1016/j.apsusc.2021.151571
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:
For NH3-selective catalytic reduction (SCR) of NO, a catalyst that exhibits effective DeNOx performance and SO2 resistance at low temperatures is necessary. In V2O5-WO3/TiO2 systems, a WO3 structure enhanced by Sb addition is effective in improving the SCR performance and SO2 resistance. In this study, the addition of Sb5+ to the WO3 structure increased NH3 adsorption due to Lewis acid formation. Furthermore, the increased electron density on the catalyst surface resulted in the formation of a higher number of W = O, which may serve as active sites for SCR, and improved oxygen mobility at low temperatures. This property subsequently caused an increase in the amount of oxygen used in SCR and improved the re-oxidation capacity in the rate-determining step to enhance the DeNOx performance. Furthermore, the NO2- produced during SCR induced the Fast-SCR reaction in V/WSb2Ti. Therefore, V/WSb2Ti produced more N-2 than that produced by V/WTi during SCR over a short time, as established using Fourier transform infrared spectroscopy and quadrupole mass spectrometer.
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页数:14
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