Influencing mechanism of temperature on the degradation of nitrobenzene in aqueous solution by ceramic honeycomb catalytic ozonation

被引:42
|
作者
Zhao, Lei [1 ]
Ma, Jun [1 ,2 ]
Sun, Zhizhong [3 ]
Liu, Huiling [1 ]
机构
[1] Harbin Inst Technol, Sch Municipal & Environm Engn, Harbin 150090, Peoples R China
[2] Harbin Inst Technol, State Key Lab Urban Water Resources & Environm, Natl Engn Res Ctr Urban Water Resources, Harbin 150090, Peoples R China
[3] Heilongjiang Univ, Sch Chem & Mat Sci, Harbin 150080, Peoples R China
基金
中国国家自然科学基金; 中国博士后科学基金;
关键词
Ceramic honeycomb; Catalytic ozonation; Nitrobenzene; Temperature; Hydroxyl radical ((OH)-O-center dot); ACTIVATED CARBON; WATER-TREATMENT; DRINKING-WATER; OXALIC-ACID; OXIDATION; OZONE; MANGANESE; EFFICIENCY; KINETICS; IRON;
D O I
10.1016/j.jhazmat.2009.01.116
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
The heterogeneous catalytic ozonation of nitrobenzene in aqueous solution has been carried out at different reaction temperatures in a semi-continuous batch reactor where ceramic honeycomb has been used as a catalyst. The experimental results indicated that the presence of ceramic honeycomb catalyst significantly improved the degradation efficiency of nitrobenzene compared to the results from non-catalytic ozonation, and the adsorption of nitrobenzene on the catalytic surface has no significant effect on its degradation efficiency. The degradation of nitrobenzene followed the pseudo-first-order kinetic model in both the processes of ozone alone and ozone/ceramic honeycomb. With the increase of reaction temperature from 278 K to 328 K, the degradation efficiency of nitrobenzene, the reaction rate constants, the utilization efficiency of ozone, the formation of hydroxyl radicals ((OH)-O-center dot) and the removal of total organic carbon (TOC) all increased in the process of ozone/ceramic honeycomb. The enhancement of reaction rate constant and the enhancement of (OH)-O-center dot formation exhibited a good correlation in the reaction temperature scope of 278-328 K. (C) 2009 Elsevier B.V. All rights reserved.
引用
收藏
页码:1119 / 1125
页数:7
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