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

催化作用 吸附 化学 X射线光电子能谱 烟气 格式化 氧气 焦炭 水蒸气 无机化学 核化学 化学工程 有机化学 工程类
作者
Xueyu Du,Caiting Li,Lingkui Zhao,Jie Zhang,Lei Gao,Jingjing Sheng,Yaoyao Yi,Jiaqiang Chen,Guangming Zeng
出处
期刊:Applied Catalysis B-environmental [Elsevier BV]
卷期号:232: 37-48 被引量:150
标识
DOI:10.1016/j.apcatb.2018.03.034
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, H2-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 Hg0 (77.51%). NO and SO2 balanced in N2 would inhibit the removal of HCHO, while the addition of 6% O2 weakened the negative effect of SO2 and NO + 6% O2 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.
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