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

微塑料 过硫酸盐 矿化(土壤科学) 激进的 降级(电信) 硫酸盐 化学 环境化学 聚对苯二甲酸乙二醇酯 化学发光 羟基自由基 化学工程 催化作用 有机化学 材料科学 电信 计算机科学 氮气 工程类 复合材料
作者
Yinghui Lin,Yuehua Zhang,Yonghao Wang,Yuancai Lv,Linyan Yang,Zhijie Chen,Bing‐Jie Ni,Xueming Chen
出处
期刊:Journal of Hazardous Materials [Elsevier BV]
卷期号:478: 135635-135635 被引量:38
标识
DOI:10.1016/j.jhazmat.2024.135635
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•- and OH, 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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