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Photocatalytic Enhancement of Metal Ion Release from Oxides in the Presence of Polystyrene: Environmental Implications in Marine Pollution
Summary
Polystyrene fragments dramatically enhanced UV-induced metal ion release from ZnO and Cu2O in aqueous media, increasing zinc concentrations by 70% and copper concentrations by 24-fold, driven by interfacial photooxidation at the polymer-oxide boundary rather than polymer degradation. This reveals a previously underappreciated mechanism by which plastic pollution amplifies metal bioavailability in marine environments, compounding the toxicological risks of microplastic contamination.
The coexistence of plastics and metal-based materials in aquatic systems introduces complex interfacial processes that influence pollutant speciation and mobility. This study investigates the role of polystyrene (PS) in promoting UV-induced dissolution of ZnO and Cu2O in aqueous media, revealing a plastic-mediated pathway for metal ion mobilization. Post-use expanded PS fragments were co-dispersed with the oxides and irradiated at 254 nm for 24 h. Ion concentrations were quantified by ICP-MS, while PS morphology and chemistry were characterized by SEM, EDX, FTIR, Raman, and DSC. The presence of PS markedly enhanced metal release, bringing Zn2+ from 29.9 to 50.6 ppm and Cu2+ from 1.1 to 26.5 ppm under irradiation, compared to minimal dissolution in the dark. Spectroscopic analyses indicated negligible polymer degradation, suggesting that enhanced dissolution arises from interfacial photooxidation and associated redox/pH microgradients at the polymer–oxide boundary. These findings demonstrate that PS may serve as a catalytic interface that accelerates UV-driven dissolution of otherwise poorly soluble metal oxides. This mechanism expands current understanding of plastic–pollutant interactions and has implications for predicting metal bioavailability and designing strategies to mitigate pollutant release in sunlit marine and coastal environments.