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Mechanistic Rolesof Microplastics in the Phototransformationof Silver Ions in Aquatic Environments

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Yuantong Chi (6989237), Dongfang Xu (1848991), Zhuomiao Liu (14124561), Fei Dang (2101855), Wenli Su (807046), Jianjun Wang (67330), Xia Liu (117318), Yanhui Dai (4162675), Tongtao Yue (2090485), Jian Zhao (219525), Zhenyu Wang (580934), Baoshan Xing (1430896)

Summary

Researchers investigated the mechanistic role of polystyrene microplastics in the phototransformation of silver ions (Ag+) in aquatic environments, finding that Ag-based nanoparticles ranging from 21.0-177.0 nm formed from Ag+ in the presence of PS microplastics after both natural light and UV irradiation. Using single-particle ICP-MS (sp-ICP-MS), they revealed that microplastics act as a photoreductive substrate that accelerates silver ion conversion to nanoparticles, potentially altering silver toxicity and bioavailability in aquatic systems.

Polymers

The role of microplastics (MPs) in transforming coexisting contaminants in aquatic environments is poorly understood. Herein, the mediation of polystyrene (PS) MPs on the phototransformation of silver ions (Ag+) was investigated. Ag-based nanoparticles (21.0–177.0 nm) formed from Ag+ in the presence of PS MPs (8.3–41.9 μm) after 40-day natural light and 96-h UV light irradiation, as detected by single-particle inductively coupled plasma mass spectrometry (sp-ICP-MS). Using a successive dissolution method, the species were identified as Ag0, Ag2O, and Ag2S nanoparticles. After 96 h of UV irradiation, Ag0 was the main nanoparticle species (93.4%), accounting for 78.0% of the total Ag. Both the MPs surface and the liquid phase were confirmed as Ag0 nanoparticle formation sites, whereas Ag2O and Ag2S were mainly formed in the liquid phase. Free radicals (superoxide radicals, oxygen-centered persistent free radicals) and oxygen-containing groups (aldehyde groups) on the MPs surface and dissolved organic matter in the liquid phase played crucial roles in Ag0 nanoparticle formation. Furthermore, sulfur species (e.g., S2– and S2O32–) in the liquid phase were responsible for the Ag2S nanoparticle formation. These findings are crucial for better understanding the environmental fate, geochemical cycle, and risk of both MPs and Ag+.

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