Molecular–level insights into the synergistic activation of peracetic acid by ultraviolet and ferrous ions for the degradation of sedimentation sludge water in drinking water treatment plants based on Fourier transform-ion cyclotron resonance mass spectrometry

[Display omitted] •The synergistic activation of PAA by UV and Fe2+ produced dominant ·OH and CH3C(O)OO·.•UV/Fe2+/PAA treatment significantly reduced the aromaticity and fluorescent abundance of SSW.•The primary reaction pathways involve oxygen addition and subsequent dehydrogenation.•Degradation of...

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Veröffentlicht in:Separation and purification technology 2025-03, Vol.355, p.129708, Article 129708
Hauptverfasser: Wang, Ya, Tong, Zhengong, Jiang, Liwen, Peng, Fangqi, Liu, Wei, Chen, Jingkai, Rao, Xuefan, Feng, Guizhen, Kang, Caixia, Fang, Lili
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Sprache:eng
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Zusammenfassung:[Display omitted] •The synergistic activation of PAA by UV and Fe2+ produced dominant ·OH and CH3C(O)OO·.•UV/Fe2+/PAA treatment significantly reduced the aromaticity and fluorescent abundance of SSW.•The primary reaction pathways involve oxygen addition and subsequent dehydrogenation.•Degradation of heteroatom-containing DOM is preferred, particularly S-DOM in SSW. Sedimentation sludge water (SSW) from sedimentation tanks in drinking water treatment plants contains significant amounts of dissolved organic matter (DOM) and precursors of disinfection byproducts, raising increasing concerns about the safety of finished water following SSW recycling. This study explores the alterations in bulk properties and molecular characteristics of DOM in SSW treated with ultraviolet (UV)/ferrous ions (Fe2+) and peracetic acid (PAA) using fluorescence spectroscopy and Fourier transform ion cyclotron resonance mass spectrometry (FT–ICR MS). The primary reactive species, hydroxyl radicals (·OH) and acylperoxy radicals (CH3C(O)OO·) achieved degradation rates of up to 82.0%, eliminating 84.5% of total fluorescent components and reducing molecular intensity and apparent molecular count by 90.9% and 69.8%, respectively. This treatment significantly reduced the aromaticity of DOM, leading to the formation of more oxidized and stable compounds. Reaction mechanisms indicate that ·OH and CH3C(O)OO· primarily facilitate oxygen addition and dehydrogenation, while CH3C(O)OO· promotes decarboxylation through weak electron transfer processes. The treatment preferentially removes complex DOM containing nitrogen and sulfur heteroatoms, which are key precursors of disinfection byproducts. These findings enhance our understanding of DOM transformations during UV/Fe2+/PAA treatment and provide valuable insights into the safe recycling of SSW.
ISSN:1383-5866
DOI:10.1016/j.seppur.2024.129708