Ozonation catalyzed by cerium supported on activated carbon for the degradation of typical pharmaceutical wastewater

被引:76
作者
Dai, Qizhou [1 ]
Wang, Jiayu [1 ]
Chen, Jun [1 ]
Chen, Jianmeng [1 ]
机构
[1] Zhejiang Univ Technol, Coll Biol & Environm Engn, Hangzhou 310032, Zhejiang, Peoples R China
基金
中国国家自然科学基金; 高等学校博士学科点专项科研基金;
关键词
Catalytic ozonation; Cerium catalyst; p-Toluenesulfonic acid; Reaction mechanism; ADVANCED OXIDATION PROCESSES; OZONE-ENHANCED OXIDATION; AQUEOUS-SOLUTION; OXALIC-ACID; COBALT CATALYSTS; SURFACE WATERS; REMOVAL; MANGANESE; NITROBENZENE; PERFORMANCE;
D O I
10.1016/j.seppur.2014.01.032
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
The catalyst of cerium supported on activated carbon (Ce/AC) for ozonation was prepared and the catalytic activity was evaluated by the degradation of p-toluenesulfonic acid (p-TSA). The results showed that Ce/AC catalyst could not only greatly enhance the degradation of p-TSA but also significantly increase the efficiency of COD removal by ozonation. The COD removal could reach 74.1% with the Ce/AC catalyst at 60 min, while the effects of activated carbon (AC) catalyst and without catalyst were only 62.4% and 50.8%, respectively. The superiority of Ce/AC catalyst was attributed to the fact that cerium increased the generation of hydroxyl radicals (OH), which could react with p-TSA and intermediate to form oxidized products rapidly. Based on the intermediates detected by GC/MS. IC and HPLC, a possible degradation pathway of p-TSA was proposed. Our aim is to provide basic data and theoretical support for pharmaceutical wastewater treatment by catalytic ozonation. (c) 2014 Published by Elsevier B.V.
引用
收藏
页码:112 / 120
页数:9
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