Comparative study of naphthalene removal in different radicals-dominated systems: Kinetics, degradation intermediates, and pathways

被引:0
|
作者
Zeng, Guilu [1 ]
Yang, Rumin [1 ]
Zhou, Zhengyuan [1 ]
Xu, Zhiqiang [1 ]
Lyu, Shuguang [1 ]
机构
[1] East China Univ Sci & Technol, State Environm Protect Key Lab Environm Risk Asses, Shanghai 200237, Peoples R China
基金
中国国家自然科学基金;
关键词
Naphthalene; Different radicals; Kinetics; Degradation intermediate; Toxicity estimation; ADVANCED OXIDATION PROCESSES; UV/H2O2; UV; UV/PERSULFATE; HYDROXYL; PRODUCTS; PEROXYMONOSULFATE; ANION; WATER;
D O I
10.1016/j.jwpe.2023.104659
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
The investigation on naphthalene (NAP) removal has been reported by increasing literatures due to its frequent detection in contaminated sites. However, the degradation intermediates of NAP in different radicals-dominated systems, as well as the estimation of their toxicities, have not been systematically illuminated. In this work, the degradation intermediates and pathways of NAP were thoroughly compared in hydroxyl radical (HO center dot) and sulfate radical (SO4-center dot) driven systems, and the radical addition was the dominant mechanism in both two sys-tems. The toxicological assessment of 27 NAP degradation intermediates were performed, suggesting that the acute toxicity of intermediates produced by SO4-center dot addition could be weakened. Moreover, a kinetic model was established to simulate the kinetics of NAP degradation at various conditions, and the simulated results were in keeping with the experimental values. The effects of chemical concentration (NAP, oxidant, HCO3-, and Cl-) and solution pH on NAP removal were elucidated. The steady-state concentrations of radicals and their contribution to NAP removal were determined by the model. Finally, the performance of significant mineralization of NAP (96.9%) in SO4-center dot-driven system confirmed the superiority of SO4-center dot-based advanced oxidation technique in the remediation of NAP-contaminated site.
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页数:12
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