Tao, D., Zhou, Y., Carter, L. orcid.org/0000-0002-1146-7920 et al. (4 more authors) (Cover date: June 2025) Overlooked formation of chlorinated coupling byproducts during phenol degradation with ferrate(VI) oxidation technology. Journal of Environmental Sciences, 152. pp. 429-441. ISSN 1001-0742
Abstract
Currently, ferrate(VI) oxidation technology (FOT) has been regarded as one of the most promising options for the degradation of emerging organic pollutants. However, the role and transformation of chloride ions (Cl−) in FOT have not been well explored. The current study aims to investigate the formation of chlorinated phenolic byproducts upon ferrate(VI) oxidation processes. The obtained results indicate that chlorides suffering ferrate(VI) attack will be transformed to active chlorine species (ACS), which will subsequently lead to the formation of highly toxic aromatic chlorinated byproducts. The identified byproducts include common chlorinated phenolic derivatives, as well as complex chlorinated oligomer byproducts with ether structures (mainly dimers and trimers). While the formation of common chlorophenols can be ascribed to the electrophilic substitution reactions mediated by ACS, the oligomer byproducts are generated via coupling reactions between chlorinated phenoxy radicals. ECOSAR software predicts that the generated chlorinated oligomer byproducts exhibit high ecotoxicological effects. As a whole, the above findings shed light on the potential risk of FOT in real practice.
Metadata
Item Type: | Article |
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Authors/Creators: |
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Copyright, Publisher and Additional Information: | © 2024 The Research Center for Eco-Environmental Sciences, Chinese Academy of Sciences. Published by Elsevier B.V. This is an author produced version of an article published in Journal of Environmental Sciences. Uploaded in accordance with the publisher's self-archiving policy. This manuscript version is made available under the CC-BY-NC-ND 4.0 license http://creativecommons.org/licenses/by-nc-nd/4.0/. |
Keywords: | Ferrate(VI) oxidation, Chlorinated oligomers, Toxicity calculation, Reaction mechanism |
Dates: |
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Institution: | The University of Leeds |
Academic Units: | The University of Leeds > Faculty of Environment (Leeds) > School of Geography (Leeds) > River Basin Processes & Management (Leeds) |
Depositing User: | Symplectic Publications |
Date Deposited: | 17 May 2024 13:22 |
Last Modified: | 08 Aug 2024 09:09 |
Published Version: | https://www.sciencedirect.com/science/article/pii/... |
Status: | Published |
Publisher: | Elsevier |
Identification Number: | 10.1016/j.jes.2024.05.024 |
Open Archives Initiative ID (OAI ID): | oai:eprints.whiterose.ac.uk:212561 |
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