Degradation kinetics of 2,4-dichlorophenol by gamma ray irradiation in the presence of ozone

被引:5
作者
Yin, Ya-Nan [1 ]
Hu, Jun [1 ]
Wang, Jian-Long [1 ,2 ]
机构
[1] Tsinghua Univ, Collaborat Innovat Ctr Adv Nucl Energy Technol, INET, Beijing 100084, Peoples R China
[2] Tsinghua Univ, Beijing Key Lab Radioact Waste Treatment, INET, Beijing 100084, Peoples R China
基金
中国国家自然科学基金;
关键词
Advanced oxidation processes; Radiolytic degradation; Chlorophenol; Decholorination; Ozonation; AQUEOUS-SOLUTION; RADIATION; WATER; 4-CHLOROPHENOL; CHLOROPHENOLS; DECOMPOSITION; REMOVAL; ACID;
D O I
10.1007/s41365-016-0074-x
中图分类号
TL [原子能技术]; O571 [原子核物理学];
学科分类号
0827 ; 082701 ;
摘要
Gamma ray-induced degradation of 2,4-dichlorophenol (DCP) in the presence of ozone has been investigated. The results show that ozone can remarkably increase the degradation rate of 2,4-DCP in aqueous solution. The degradation kinetics of 2,4-DCP can be described by the first-order reaction model, and the rate constant was 0.443, 0.490 and 1.247 h(-1), respectively, for gamma-ray irradiation only, gamma- ray irradiation + 13 mg/L O-3 and gamma- ray irradiation + 30 mg/L O-3. High-performance liquid chromatography analysis shows that the dechlorinated products are 4-chlorophenol, 2-chlorophenol and phenol; and the oxidation products are hydroquinone, benzoquinone, maleic, fumaric, acrylic, malonic, oxalic, acetic and formic acids. The possible pathways for 2,4-DCP degradation involving all these oxidation products are tentatively proposed. Combining gamma-ray irradiation with ozonation is a promising technology for removing toxic pollutants from water and wastewater.
引用
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页数:5
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