Peracetic acid combined with ultraviolet for ibuprofen degradation: Activation mechanism and reactive species contribution

被引:7
|
作者
Fan, Gongduan [1 ,2 ]
Li, Yujian [1 ]
Du, Banghao [1 ,3 ]
Yao, Lei [1 ]
Cai, Chenjian [1 ]
Li, Hao [1 ,4 ]
Chen, Shoubin [4 ]
Zou, Jianyong [5 ]
Hong, Zhanglin [6 ]
Xu, Kai-Qin [1 ]
机构
[1] Fuzhou Univ, Coll Civil Engn, Fuzhou 350116, Fujian, Peoples R China
[2] Fujian Prov Key Lab Elctrochem Energy Storage Mat, Fuzhou 350002, Fujian, Peoples R China
[3] Shandong Agr Univ, Coll Water Conservancy & Civil Engn, Tai An 271018, Peoples R China
[4] Fuzhou City Construct Design & Res Inst Co Ltd, Fuzhou 350001, Fujian, Peoples R China
[5] Anhui Urban Construct Design Inst Co Ltd, Hefei 230051, Anhui, Peoples R China
[6] China Construct Third Bur First Engn Co Ltd, Wuhan 430040, Hubei, Peoples R China
基金
中国国家自然科学基金;
关键词
UV; PAA; Reactive oxygen species; Pharmaceuticals; Degradation pathways; Toxicity analysis; UV/PERACETIC ACID; PEROXYL RADICALS; KINETICS; UV/H2O2; WATER; PHARMACEUTICALS; DECOMPOSITION; PRODUCTS; ACETATE;
D O I
10.1016/j.psep.2023.09.012
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
As an emerging advanced oxidation technology, ultraviolet/peracetic acid (UV/PAA) shows great potential in removing pharmaceuticals and personal care products (PPCPs) in the field of wastewater treatment. In this work, ibuprofen (IBP) was chosen as the contaminant to study the degradation effects and PAA activation mechanisms by UV irradiation. The experimental results showed that UV/PAA had an excellent degradation efficiency (99.22 %) of IBP after 15 min reaction, and the synergistic effect between UV and PAA was also observed. Increasing the dosage of PAA caused the increase in IBP degradation reaction rate. Under acidic conditions, the increase in pH values increased the degradation reaction rate, whereas the opposite was true in alkaline conditions. In addition, the coexisting substrates (e.g., NO3- , CO32-, Ca2+, and HA) could exert inhibition on the degradation. Quenching experiments were carried out using various quenchers to identify reactive oxygen species (ROSs) in the system. The results demonstrated that center dot OH and carbon centered radicals (R-C center dot) played a dominant part in the degradation, and the contribution of CH3C(O)OO center dot,center dot O2- , CH3C(O)O center dot, center dot OH, and direct photolysis were estimated to be 29.9 %, 26.9 %, 21.5 %, 14.5 %, and 7.2 %, respectively. The results of IBP intermediates identification indicated that the degradation process was mainly related to its side chain decarboxylation, oxidative dehydrogenation, demethylation, and the oxidation of the aromatic ring. Furthermore, Toxicity Estimation Software Tool (T.E.S.T.) and ECOSAR were applied to evaluate the toxicity of the intermediate products was further evaluated. This study enriched the understanding of the PAA activation mechanism by UV involved, and improved the theory and technology of removing PPCPs by UV/PAA process.
引用
收藏
页码:157 / 167
页数:11
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