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Identification of the arsenic resistance on MoO3 doped CeO2/TiO2 catalyst for selective catalytic reduction of NOx with ammonia
被引:72
作者:
Li, Xiang
[1
]
Li, Xiansheng
[1
]
Li, Junhua
[1
]
Hao, Jiming
[1
]
机构:
[1] Tsinghua Univ, Sch Environm, State Key Joint Lab Environm Simulat & Pollut Con, Beijing 100084, Peoples R China
基金:
中国博士后科学基金;
中国国家自然科学基金;
关键词:
NH3-SCR;
As poisoning;
CO4+ to Ce3+ redox cycle;
MoO3;
NOx adsorbed species;
MIXED-OXIDE CATALYST;
TUNGSTEN-OXIDE;
SCR CATALYSTS;
ACTIVE-SITES;
NITRIC-OXIDE;
NH3;
MECHANISM;
DEACTIVATION;
PERFORMANCE;
ACIDITY;
D O I:
10.1016/j.jhazmat.2016.07.058
中图分类号:
X [环境科学、安全科学];
学科分类号:
08 ;
0830 ;
摘要:
Arsenic resistance on MoO3 doped CeO2/TiO2 catalysts for selective catalytic reduction of NOx with NH3 (NH3-SCR) is investigated. It is found that the activity loss of CeO2-MoO3/TiO2 caused by As oxide is obviousiess than that of CeO2/TiO2 catalysts. The fresh and poisoned catalysts are compared and analyzed using XRD, Raman, XPS, H-2-TPR and in situ DRIFTS. The results manifest that the introduction of arsenic oxide to CeO2/TiO2 catalyst not only weakens BET surface area, surface acid sites and adsorbed NOx species, but also destroy the redox circle of Ce4+ to Ce3+ because of interaction between Ce and As. When MoO3 is added into CeO2/TiO2 system, the main SCR reaction path are found to be changed from the reaction between coordinated NH3 and ad-NOx species to that between an amide and gaseous NO. Additionally, for CeO2-MoO3/TiO2 catalyst, As toxic effect on active sites CeO2 can be released because of stronger As-Mo interaction. Moreover, not only are the reactable Bronsted and Lewis acid sites partly restored, but the cycle of Ce4+ to Ce3+ can also be free to some extent. (C) 2016 Published by Elsevier B.V.
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页码:615 / 622
页数:8
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