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在非均相电芬顿活化过硫酸盐氧化体系中,通过硫酸根和羟基自由基的协同作用实现聚对苯二甲酸乙二酯微塑料的高效降解与矿化。

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.

作者信息

Lin Yinghui, Zhang Yuehua, Wang Yonghao, Lv Yuancai, Yang Linyan, Chen Zhijie, Ni Bing-Jie, Chen Xueming

机构信息

College of Environment and Safety Engineering, Fuzhou University, Fuzhou 350116, China.

School of Resources and Environmental Engineering, East China University of Science and Technology, Shanghai 200237, China.

出版信息

J Hazard Mater. 2024 Oct 5;478:135635. doi: 10.1016/j.jhazmat.2024.135635. Epub 2024 Aug 24.

Abstract

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 FeS-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 SO 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.

摘要

水体中聚对苯二甲酸乙二酯(PET)微塑料(MPs)的存在对环境和人类构成了相当大的威胁。在这项工作中,提出了一种以FeS改性碳毡为阴极的非均相电芬顿活化过硫酸盐氧化体系(简称为EF-SR)用于高效降解PET MPs。结果表明:i)EF-SR体系在12小时后去除了100mg/L PET的91.3±0.9%,同时[Fe]的损失量极少(<0.07%);ii)在EF-SR体系中,溶解有机物和纳米塑料首先形成并积累,然后迅速被消耗。除了表面形态的破坏,EF-SR处理后PET的表面结构也有显著变化。除了出现O-H键外,C-O/C=O与C-C的比例从0.25增加到0.35,这证明了PET主链的断裂以及PET表面含氧基团的形成。通过验证SO和OH的参与及贡献,提出了三种可能的途径来描述EF-SR体系中PET通过链断裂和氧化实现完全矿化的降解过程。

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