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Adsorption of Cu2+ by UV aged polystyrene in aqueous solution

Ecotoxicology and Environmental Safety 2022 73 citations ? Citation count from OpenAlex, updated daily. May differ slightly from the publisher's own count.
Chao Chen, Wei Feng, Liang Ye, Yating Wang, Lulu Long, Changlian Xu, Yinlong Xiao, Yinlong Xiao, Jun Wu, Min Xu, Jinsong He, Gang Yang

Summary

UV-aged polystyrene microplastics showed altered surface chemistry and enhanced adsorption of copper ions compared to virgin particles, with the degree of adsorption increasing with aging duration. The findings indicate that environmental weathering transforms microplastics into more potent heavy metal carriers, intensifying their role as pollutant vectors.

Polymers

Microplastics are the critical carriers of heavy metals in the environment. Thus, investigating the adsorption mechanisms between the microplastics and heavy metals is helpful to understand the migration and transformation pattern of the heavy metals in the environment. The adsorption of microplastics towards heavy metals can be largely affected by natural aging (e.g., UV-aging), environmental pH, and salinity. In this study, the adsorption of polystyrene (PS) towards Cu and the effects of UV-aging, environment pH, and salinity on the adsorption were systematically investigated. The results show that the adsorption capacity of PS towards Cu increased with the UV-aging time, as UV-aging increased the microcracks and oxygen-containing functional groups on the surface of the PS. Adsorption kinetics data followed the pseudo-second-order model, indicating that the interaction between PS and Cu is chemical adsorption. Adsorption isotherms data could be well-described by both the Langmuir and Freundlich models, indicating that the adsorption was multilayer adsorption. As the solution pH and salinity can influence the surface charge of the PS, they could also affect the performance of the PS on Cu adsorption. High pH facilitated the adsorption of PS towards Cu, while high salinity (above 1‰) inhibited the adsorption.

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