Highly efficient degradation of perfluoroalkyl substances (PFAS) by a novel polytetrafluoroetylene piezocatalyst.

J Hazard Mater

School of Materials, Sun Yat-Sen University, Shenzhen 518107, China; State Key Laboratory of Optoelectronic Materials and Technologies, Sun Yat-Sen University, Guangzhou 510275, China. Electronic address:

Published: January 2025

AI Article Synopsis

  • PFAS are toxic pollutants that are tough to break down due to strong chemical bonds.
  • Researchers found a method using PTFE, a harmless material, as a piezocatalyst to degrade PFAS effectively.
  • This technique achieved a 93.4% degradation of PFOA and works on other PFAS compounds, offering a promising solution for cleaning contaminated water.

Article Abstract

Perfluoroalkyl substances (PFAS) are environmentally persistent, bioaccumulative and toxic pollutants. However, thorough degradation of PFAS remains exceptionally difficult due to the high dissociation energy of the C-F bond. Here, we report a viable strategy to markedly degrade PFAS completely by capitalizing on a harmless polytetrafluoroetylene (PTFE) as a piezocatalyst. Remarkably, perfluorooctanoic acid (PFOA), as one of the widely used PFAS, was almost completely removed with a degradation rate of 93.4 % and a defluorination rate of 91.5 % by the ultrasound excitation of PTFE for 1 h. On the basis of the intermediate analysis, we proposed an oxidation mechanism for the piezocatalytic PFOA degradation. Furthermore, this strategy was also efficient for the degradation of perfluoroheptanoic acid (PFNA), perfluorooctane sulfonate (PFOS) and hexafluoropropylene oxide dimer acid (Gen-X), implying its effectiveness to remediate water containing multiple PFAS. Impressively, due to the diverse energy gap between HOMO and LUMO energy of various PFAS, the degradation reaction kinetics of different PFAS are of significant difference. This study provides the deep insight into the piezocatalytic technique for the remediation of persistent and disparate PFAS.

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Source
http://dx.doi.org/10.1016/j.jhazmat.2025.137317DOI Listing

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