微塑料
降级(电信)
阳极
聚乙烯
焦耳加热
材料科学
焦耳(编程语言)
化学工程
电化学
炭黑
环境化学
复合材料
化学
电极
计算机科学
工程类
物理化学
电信
功率(物理)
天然橡胶
物理
量子力学
作者
Dan Shao,Weipeng Zhao,Shiyu Ji,Changan Yang,Jikun Zhang,Ruixi Guo,Bo Zhang,Wei Lyu,Jiangtao Feng,Hao Xu,Wei Yan,Haojie Song
标识
DOI:10.1016/j.apcatb.2024.124281
摘要
Polyethylene (PE) microplastics (MPs) in water was rapidly degraded using a "Joule heat assisting electrochemical degradation" strategy. In a tailor-made reactor, PE MPs were captured by anode, being softened or even melted by the interface Joule heat, enabling direct electron transfer and making the maximum use of short-lived active species. Within a few hours, above 99 % of PE MPs (∼ 1 g·L−1) vanished, and residual solid products with higher carbonyl index (CI) and O/C ratio inclined to combine, avoiding creating more harmful nanoplastics (NPs), just leaving a few low-threatening soluble products with unsaturated carbon chains. Compared with SO42- and S2O82-, the presence of Cl- water matrix could facilitate the chain-scission degradation and make solid products fusion more significant. After proposing a novel MPs degradation mechanism and verifying the universality of this novel strategy by degrading other five kinds of MPs. Subsequently, a techno-economic analysis was conducted.
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