Heterogenous Perfluorooctanoic Acid Degradation with Molecular Copper Electrocatalyst

11 September 2024, Version 1
This content is a preprint and has not undergone peer review at the time of posting.

Abstract

The increasing emission of chemically resistant perfluorinated compounds (PFCs) into the natural environment, along with their global presence in natural and treated waters and in both human and animal organisms, presents a significant environmental challenge. A cost-effective method for the successful degradation of perfluorooctanoic acid (PFOA) in aqueous solutions is crucial. Electrochemical oxidation has been demonstrated to uniquely degrade PFOA. In this study, we present a molecular copper (I) complex, [CuT2]•ClO4, in a heterogeneous aqueous system capable of degrading PFOA by up to 84% with a defluorination rate of 91% through anodic oxidation using controlled current electrolysis (CCE). Furthermore, we utilized ESI/MS to identify the degradation products from the electrochemical oxidation of PFOA. The shortening of the PFOA chain results in reduced toxicity due to decreased persistence. Thus, the findings of this study show that the [CuT2]•ClO4 complex is an efficient catalyst for the degradation and defluorination of PFOA.

Supplementary materials

Title
Description
Actions
Title
Supporting Information
Description
Instrumental information, experimental details, and supporting figures.
Actions

Comments

Comments are not moderated before they are posted, but they can be removed by the site moderators if they are found to be in contravention of our Commenting Policy [opens in a new tab] - please read this policy before you post. Comments should be used for scholarly discussion of the content in question. You can find more information about how to use the commenting feature here [opens in a new tab] .
This site is protected by reCAPTCHA and the Google Privacy Policy [opens in a new tab] and Terms of Service [opens in a new tab] apply.