Degradation and detoxification of 6PPD-quinone in water by ultraviolet-activated peroxymonosulfate: Mechanisms, byproducts, and impact on sediment microbial community

•6PPD-Q can be completely removed when the initial ratio of PMS to 6PPD-Q was 60:1.••OH and SO4•− played a dominant role in 6PPD-Q degradation in the UV/PMS system.•Twenty-one degradation products of 6PPD-Q were identified by UPLCOrbitrap-MS/MS.•All identified products exhibited lower predicted toxi...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Water research (Oxford) 2024-10, Vol.263, p.122210, Article 122210
Hauptverfasser: Yu, Wenyan, Tang, Shaoyu, Wong, Jonathan W.C., Luo, Zhujun, Li, Zongrui, Thai, Phong K., Zhu, Minghan, Yin, Hua, Niu, Junfeng
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
Beschreibung
Zusammenfassung:•6PPD-Q can be completely removed when the initial ratio of PMS to 6PPD-Q was 60:1.••OH and SO4•− played a dominant role in 6PPD-Q degradation in the UV/PMS system.•Twenty-one degradation products of 6PPD-Q were identified by UPLCOrbitrap-MS/MS.•All identified products exhibited lower predicted toxicity compared to 6PPD-Q.•UV/PMS possesses superior detoxifying capability of 6PPD-Q to sediment microbiome. N-(1,3-dimethylbutyl)-N′-phenyl-p-phenylenediamine quinone (6PPD-Q) has been identified to induce acute toxicity to multifarious aquatic organisms at exceptionally low concentrations. The ubiquity and harmful effects of 6PPD-Q emphasize the critical need for its degradation from water ecosystems. Herein, we explored the transformation of 6PPD-Q by an ultraviolet-activated peroxymonosulfate (UV/PMS) system, focusing on mechanism, products and toxicity variation. Results showed that complete degradation of 6PPD-Q was achieved when the initial ratio of PMS and 6PPD-Q was 60:1. The quenching experiments and EPR tests indicated that SO4•− and •OH radicals were primarily responsible for 6PPD-Q removal. Twenty-one degradation products were determined through high-resolution orbitrap mass spectrometry, and it was postulated that hydroxylation, oxidative cleavage, quinone decomposition, ring oxidation, as well as rearrangement and deamination were the major transformation pathways of 6PPD-Q. Toxicity prediction revealed that all identified products exhibited lower acute and chronic toxicities to fish, daphnid and green algae compared to 6PPD-Q. Exposure experiments also uncovered that 6PPD-Q considerably reduced the community diversity and altered the community assembly and functional traits of the sediment microbiome. However, we discovered that the toxicity of 6PPD-Q degradation solutions was effectively decreased, suggesting the superior detoxifying capability of the UV/PMS system for 6PPD-Q. These findings highlight the underlying detrimental impacts of 6PPD-Q on aquatic ecosystems and enrich our understanding of the photochemical oxidation behavior of 6PPD-Q. [Display omitted]
ISSN:0043-1354
1879-2448
1879-2448
DOI:10.1016/j.watres.2024.122210