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The sorption kinetics and isotherms of sulfamethoxazole with polyethylene microplastics
Summary
The sorption of the antibiotic sulfamethoxazole onto polyethylene microplastics was well described by pseudo-second-order kinetics and Freundlich isotherms, with the process controlled by partitioning into the polymer matrix. The study demonstrates that microplastics can accumulate antibiotics from seawater, raising concerns about contributing to antibiotic resistance through environmental spread of these compounds.
Microplastics and sulfamethoxazole coexist ubiquitously in the marine environment, and microplastics tend to sorb organic pollutants from the surrounding environment. Here, the sorption kinetics and isotherms of sulfamethoxazole on polyethylene (PE) microplastics closely fitted a pseudo-second-order model (R = 0.98) and linear model (R = 0.99), respectively, indicating that the sorption process was partition-dominant interaction. The main binding mechanism was possibly the van der Waals interaction for hydrophilic sulfamethoxazole onto hydrophobic PE microplastics. The effects of pH, dissolved organic matter and salinity on sorption behavior were also studied. The sorption behavior of sulfamethoxazole on PE microplastics was not significantly influenced by pH and salinity, probably because the electrostatic repulsion played a minor role. In addition, the negligible effect of dissolved organic matter was attributed to the greater affinity of sulfamethoxazole to PE microplastics than to dissolved organic matter. Our results demonstrated that PE microplastics may serve as a carrier for sulfamethoxazole in the aquatic environment.
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