Efficient degradation and mineralization of polyethylene terephthalate microplastics by the synergy of sulfate and hydroxyl radicals in a heterogeneous electro-Fenton-activated persulfate oxidation system

被引:0
|
作者
Lin, Yinghui [1 ]
Zhang, Yuehua [1 ]
Wang, Yonghao [1 ]
Lv, Yuancai [1 ]
Yang, Linyan [2 ]
Chen, Zhijie [3 ]
Ni, Bing-Jie [3 ]
Chen, Xueming [1 ]
机构
[1] Fuzhou Univ, Coll Environm & Safety Engn, Fuzhou 350116, Peoples R China
[2] East China Univ Sci & Technol, Sch Resources & Environm Engn, Shanghai 200237, Peoples R China
[3] Univ New South Wales, Sch Civil & Environm Engn, Sydney, NSW 2052, Australia
关键词
Electro-Fenton; Hydroxyl radical; Microplastics; Polyethylene terephthalate; Sulfate radical; PEROXYMONOSULFATE;
D O I
10.1016/j.jhazmat.2024.135635
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
The presence of polyethylene terephthalate (PET) microplastics (MPs) in waters has posed considerable threats to the environment and humans. In this work, a heterogeneous electro-Fenton-activated persulfate oxidation system with the FeS2-modified carbon felt as the cathode (abbreviated as EF-SR) was proposed for the efficient degradation of PET MPs. The results showed that i) the EF-SR system removed 91.3 +/- 0.9 % of 100 mg/L PET after 12 h at the expense of trace loss (< 0.07 %) of [Fe] and that ii) dissolved organics and nanoplastics were first formed and accumulated and then quickly consumed in the EF-SR system. In addition to the destruction of the surface morphology, considerable changes in the surface structure of PET were noted after EF-SR treatment. On top of the emergence of the O-H bond, the ratio of C-O/C=O to C-C increased from 0.25 to 0.35, proving the rupture of the backbone of PET and the formation of oxygen-containing groups on the PET surface. With the verified involvement and contributions of SO4 center dot- and (OH,)-O-center dot three possible paths were proposed to describe the degradation of PET towards complete mineralization through chain cleavage and oxidation in the EF-SR system.
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页数:8
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