Promotional removal of HCHO from simulated flue gas over Mn-Fe oxides modified activated coke

被引:142
|
作者
Du, Xueyu [1 ,2 ]
Li, Caiting [1 ,2 ]
Zhao, Lingkui [1 ,2 ,3 ]
Zhang, Jie [1 ,2 ]
Gao, Lei [1 ,2 ]
Sheng, Jingjing [1 ,2 ]
Yi, Yaoyao [1 ,2 ]
Chen, Jiaqiang [1 ,2 ]
Zeng, Guangming [1 ,2 ]
机构
[1] Hunan Univ, Coll Environm Sci & Engn, Changsha 410082, Hunan, Peoples R China
[2] Hunan Univ, Minist Educ, Key Lab Environm Biol & Pollut Control, Changsha 410082, Hunan, Peoples R China
[3] Xiangtan Univ, Coll Environm Sci & Resources, Xiangtan 411105, Peoples R China
关键词
HCHO; Mn-Fe oxides; Activated coke; Catalytic removal; EFFICIENT CATALYTIC REMOVAL; ELEMENTAL MERCURY REMOVAL; COMPLETE OXIDATION; ROOM-TEMPERATURE; GASEOUS FORMALDEHYDE; SELECTIVE OXIDATION; AMBIENT-TEMPERATURE; ORGANIC POLLUTANTS; GOLD CATALYSTS; SPINEL FERRITE;
D O I
10.1016/j.apcatb.2018.03.034
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
A series of MnxFey/AC catalysts synthesized by impregnation method were investigated on the efficient and stable removal of HCHO in the fix-bed reactor. Extensive characterizations, BET, SEM, XRD, H-2-TPR, XPS and FT-IR, were conducted to study the physicochemical properties, HCHO oxidation and surface reaction of catalysts. The optimal Mn0.75Fe6.02/AC showed enhanced HCHO removal efficiency of 98.30%, as well as excellent performance for simultaneous removal of HCHO (89.96%) and Hg-0 (77.51%). NO and SO2 balanced in N-2 would inhibit the removal of HCHO, while the addition of 6% O-2 weakened the negative effect of SO2 and NO + 6% O-2 facilitated the removal of HCHO. Besides, the slight promotion effect of water vapor was contributed to the regeneration of consumed -OH via the activation of surface oxygen by adsorbed H2O. Characterization results indicated that Mn0.75Fe6.02/AC possessed larger BET surface area, well-developed porosity and better dispersion of active components. Mn0.75Fe6.02/AC exhibited higher reducibility due to the synergistic effect between MnOx and FeOx and the interaction between Mn-Fe oxides and AC support. At the same time, the oxygen-containing functional groups (C-O-, COO), abundant active surface oxygen and -OH facilitated both adsorption and oxidation of HCHO. Besides, the formate and carbonate intermediates formed on the surface of Mn0.75Fe6.02/AC in HCHO removal process, which could be further oxidized into CO2 and H2O. On the basis of above investigations, the mechanism of enhanced HCHO catalytic removal over MnxFey/AC was proposed.
引用
收藏
页码:37 / 48
页数:12
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