Simultaneous NO Reduction and Hg0 Oxidation over La0.8Ce0.2MnO3 Perovskite Catalysts at Low Temperature

被引:46
|
作者
Yang, Jianping [1 ]
Zhang, Mingguang [1 ]
Li, Hailong [1 ]
Qu, Wenqi [1 ]
Zhao, Yongchun [2 ]
Zhang, Junying [2 ]
机构
[1] Cent S Univ, Sch Energy Sci & Engn, Changsha 410083, Hunan, Peoples R China
[2] Huazhong Univ Sci & Technol, Sch Energy & Power Engn, State Key Lab Coal Combust, Wuhan 430074, Hubei, Peoples R China
基金
中国国家自然科学基金;
关键词
COMBUSTION FLUE-GAS; ELEMENTAL MERCURY OXIDATION; CUCL2 MODIFIED MAGNETOSPHERES; SIMULTANEOUS REMOVAL; FLY-ASH; CUO-CEO2/TIO2; CATALYST; OXYFUEL COMBUSTION; MNOX/TIO2; EFFICIENT REMOVAL; SO2; RESISTANCE;
D O I
10.1021/acs.iecr.8b01431
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
La(1-x)A(x)Mn(1-y)B(y)O(3) (A = Ca, Sr and Ce, B = Cu, Co and Fe, x = 0/0.2, y = 0/0.2) perovskite catalysts were employed for simultaneous NO and Hg-0 removal. The perovskite structure is beneficial for low temperature catalysis. The substitution of A-site cations with cerium (Ce) cations significantly improved the catalytic activity of perovskite catalyst. 90% NO conversion and 98% Hg-0 oxidation was attained using La0.8Ce0.2MnO3 catalyst at 200 degrees C. Hg-0 oxidation posed negligible effect on NO reduction. Compared to the N-2 plus 4% O-2 atmosphere, Hg-0 oxidation was significantly facilitated by selective catalytic reduction atmosphere. The enhancement in Hg-0 oxidation was probably attributed to NO2 originated from NO. Furthermore, a possible reaction mechanism was proposed, in which surface oxygen, Mn(4+ )and Ce4+ contributed to NO and Hg-0 removal. Such knowledge provides useful information for the development of effective and economical NO and Hg-0 removal technology for power plants.
引用
收藏
页码:9374 / 9385
页数:12
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