Chlorobenzene oxidation using ozone over iron oxide and manganese oxide catalysts

NCU Institutional Repository > 工學院 > 環境工程研究所 > 期刊論文 > Item 987654321/50137

jsp.display-item.identifier=請使用永久網址來引用或連結此文件: http://ir.lib.ncu.edu.tw/handle/987654321/50137

题名:	Chlorobenzene oxidation using ozone over iron oxide and manganese oxide catalysts
作者:	Wang,HC;Liang,HS;Chang,MB
贡献者:	環境工程研究所
关键词:	CO OXIDATION;CARBON-MONOXIDE;DECOMPOSITION;BENZENE;ELIMINATION;1,2-DICHLOROBENZENE;ALPHA-FE2O3;COMPOSITES;PCDD/PCDF;BEHAVIOR
日期:	2011
上传时间:	2012-03-27 17:04:18 (UTC+8)
出版者:	國立中央大學
摘要:	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.
關聯:	JOURNAL OF HAZARDOUS MATERIALS
显示于类别:	[環境工程研究所 ] 期刊論文

文件中的档案:

档案	描述	大小	格式	浏览次数
index.html		0Kb	HTML	672	检视/开启

在NCUIR中所有的数据项都受到原著作权保护.

社群 sharing

数据加载中.....