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    Please use this identifier to cite or link to this item: http://ir.lib.ncu.edu.tw/handle/987654321/50137


    Title: Chlorobenzene oxidation using ozone over iron oxide and manganese oxide catalysts
    Authors: Wang,HC;Liang,HS;Chang,MB
    Contributors: 環境工程研究所
    Keywords: CO OXIDATION;CARBON-MONOXIDE;DECOMPOSITION;BENZENE;ELIMINATION;1,2-DICHLOROBENZENE;ALPHA-FE2O3;COMPOSITES;PCDD/PCDF;BEHAVIOR
    Date: 2011
    Issue Date: 2012-03-27 17:04:18 (UTC+8)
    Publisher: 國立中央大學
    Abstract: A low-temperature catalytic oxidation of chlorobenzene (CB) has been performed at temperatures of 60-210 degrees C using ozone (O(3)) over iron oxide and manganese oxide, respectively. In the absence of ozone. CB conversion achieved with these two catalysts at 200 degrees C was below 10%. However, addition of 1200 ppm ozone results in a remarkable increase in CB conversion and the conversion reaches 91.7% at 150 degrees C for iron oxide, while 81.5% conversion is achieved with manganese oxide at 90 degrees C. The activation energy of manganese oxide (48 kJ mol(-1)) is higher than that of iron oxide (43 kJ mol(-1)) without ozone. However, as ozone is added, the activation energy is significantly reduced to 20.0 kJ mol(-1) for iron oxide. CO and CO(2) are the only carbon-containing products detected in the effluent gas stream. For the long-term test, no obvious deactivation was found in iron oxide and ozone. However, in the case of manganese oxide and ozone. 3% reduction of CB conversion was observed. Slight deactivation might be attributed to a small amount of reaction byproducts (carboxylic acid species) and residual chloride (MnCl(2)) being deposited on the active sites of the catalysts. (C) 2010 Elsevier B.V. All rights reserved.
    Relation: JOURNAL OF HAZARDOUS MATERIALS
    Appears in Collections:[環境工程研究所 ] 期刊論文

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