Catalytic Combustion of Vinyl Chloride Emission over CeO2-MnOx Catalyst

被引:7
|
作者
Wan Yiling [1 ,2 ]
Zhang Chuanhui [1 ]
Guo Yanglong [1 ]
Guo Yun [1 ]
Lu Guanzhong [1 ]
机构
[1] E China Univ Sci & Technol, Res Inst Ind Catalysis, Shanghai 200237, Peoples R China
[2] Guangdong Ocean Univ, Coll Sci, Zhanjiang 524088, Guangdong, Peoples R China
基金
国家高技术研究发展计划(863计划);
关键词
cerium; manganese; composite oxide; vinyl chloride; catalytic combustion; solid solution; oxygen species; MIXED-OXIDE CATALYSTS; DEEP OXIDATION; CHLOROBENZENE; 1,2-DICHLOROETHANE; PURIFICATION; CEO2;
D O I
10.3724/SP.J.1088.2012.11003
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
CeO2-MnOx catalyst samples with different Mn/(Ce+Mn) molar ratios (0, 1/4, 1/2, 3/4, and 1) prepared by the citric acid (CA) sol-gel method were studied for catalytic combustion of vinyl chloride (VC) emission. The effects of preparation conditions and operation parameters on the catalytic performance of CeO2-MnOx., were investigated. The catalyst samples were characterized by N-2 adsorption, X-ray diffraction (XRD), and H-2 temperature-programmed reduction (H-2-TPR). In the catalytic combustion of VC over CeO2-MnOx, the products containing HCl, CO2, and H2O were produced and there were no byproducts such as chlorohydrocarbons and chlorine. The CeO2-MnOx catalyst with the molar ratio of CA:Mn:Ce = 0.30:0.50:0.50 showed the best catalytic performance and had better operating flexibility over the ranges of gas hourly space velocity (GHSV) of 10000-30000 h(-1) and VC concentration of 0.05%-0.15%. The temperatures at 50% conversion (110 degrees C) and at 99% conversion (220 degrees C) were achieved at VC concentration of 0.1% and GHSV of 15000 h(-1). XRD characterization indicated that only the characteristic diffraction peaks of CeO2 with the cubic fluorite structure appeared and no characteristic diffraction peaks of MnOx species appeared over CeO2-MnOx catalyst. XRD and H-2-TPR results indicated that Mn ions were incorporated into the CeO2 lattice to form Ce-Mn-O solid solution, which was favorable for improving the reactivity of active oxygen species on the catalyst surface and thereby enhanced the catalyst activity.
引用
收藏
页码:557 / 562
页数:6
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