JOURNAL ARTICLE
Ultraviolet‐enhanced Fe0‐activated H2O2 process for the removal of refractory organic matter from landfill leachate: Performance and mechanism.
Published In: Water Environment Research (10614303), 2025, v. 97, n. 2. P. 1 1 of 3
Database: Academic Search Ultimate 2 of 3
Authored By: Zhao, Guonan; Feng, Ke 3 of 3
Abstract
The Fenton‐like process, utilizing zero‐valent iron (Fe0) and hydrogen peroxide (H2O2), is employed to degrade refractory organic matter in membrane bioreactor (MBR) effluent derived from landfill leachate. However, the rate‐limiting Fe2+/Fe3+ redox step diminishes treatment efficacy and generates substantial iron sludge. This study elucidates the mechanism by which ultraviolet (UV) irradiation augments the Fe0/H2O2 process for the removal of refractory organic matter in MBR effluent. The results show that the UV‐ enhanced H2O2 process effectively disrupts the aromatic structure of organic compounds, reducing molecular weight, degree of polymerization, and humification. Compared with the Fe0/H2O2 process, the removal efficiency of UV254, color number, and total organic carbon in the effluent treated by the UV/Fe0/H2O2 process increased by 24.16%, 14.62%, and 57.46%, respectively. Concurrently, the generation of iron sludge was reduced by 21.6%. This enhancement is primarily attributed to UV's ability to intensify the Fe2+/Fe3+ redox cycle and expedite the surface corrosion of Fe0, yielding more iron oxides. This accelerates the decomposition of H2O2, generating a higher quantity of •OH through both homogeneous and heterogeneous Fenton‐like reactions. The refractory organic matter is removed through the oxidation by •OH, as well as the adsorption and precipitation facilitated by iron‐based colloids. Practitioner Points: UV promotes Fe0/H2O2 process to degrade refractory organic matter in MBR effluent.UV promotes Fe0 to dissolve more Fe2+ and the redox cycle of Fe2+ and Fe3+.The dosage of H2O2 or Fe0 influences the treatment effect of the process. [ABSTRACT FROM AUTHOR]
Additional Information
- Source:Water Environment Research (10614303). 2025/02, Vol. 97, Issue 2, p1
- Document Type:Article
- Subject Area:Chemistry
- Publication Date:2025
- ISSN:1061-4303
- DOI:10.1002/wer.70022
- Accession Number:183851373
- Copyright Statement:Copyright of Water Environment Research (10614303) is the property of Wiley-Blackwell and its content may not be copied or emailed to multiple sites without the copyright holder's express written permission. Additionally, content may not be used with any artificial intelligence tools or machine learning technologies. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)
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