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Methylmercury sorption to polyethylene terephthalate (PET) fibers and relevance to environmental exposure

Environmental Toxicology and Chemistry 2025 9 citations ? Citation count from OpenAlex, updated daily. May differ slightly from the publisher's own count. Score: 63 ? 0–100 AI score estimating relevance to the microplastics field. Papers below 30 are filtered from public browse.
H. Frost, Tom Bond, Tom Bond, H. Frost, H. Frost, Tom Sizmur, Mark L. Mallory H. Frost, M. Felipe-Sotelo, Tom Bond, Tom Bond, Tom Bond, Tom Bond, Tom Bond, Tom Bond, Tom Sizmur, Tom Bond, Mark L. Mallory Tom Bond, Mark L. Mallory Tom Sizmur, Mark L. Mallory M. Felipe-Sotelo, M. Felipe-Sotelo, M. Felipe-Sotelo, Mark L. Mallory Mark L. Mallory M. Felipe-Sotelo, M. Felipe-Sotelo, Mark L. Mallory Mark L. Mallory Mark L. Mallory Mark L. Mallory Tom Bond, Mark L. Mallory Mark L. Mallory Mark L. Mallory Mark L. Mallory Mark L. Mallory Nelson J. O’Driscoll, Mark L. Mallory Mark L. Mallory Mark L. Mallory Mark L. Mallory Mark L. Mallory Mark L. Mallory Mark L. Mallory Mark L. Mallory Mark L. Mallory

Summary

Researchers measured how methylmercury, a toxic form of mercury, sticks to polyester (PET) microplastic fibers released from clothing. They found that while the fibers do absorb some mercury, the amount is about 10,000 times lower than what naturally occurs on tiny organisms at the base of the food web. This is actually reassuring news, suggesting that PET microplastic fibers in the environment do not significantly increase mercury exposure for organisms that accidentally eat them.

Polymers

Considerable amounts of polyethylene terephthalate (PET) microplastic fibers are released into the environment by the laundering of polyester clothing. Microplastic fibers can be ingested by organisms in the environment. Therefore, it has been suggested that microplastic fibers act as vectors for adsorbed contaminants, which are subsequently desorbed in the gut of the organism. We undertook sorption isotherm experiments at pH 6, 7, and 8 to quantify the sorption of methylmercury (MeHg) to PET fibers. Sorption isotherms were fit to Langmuir, Freundlich, and Brunauer-Emmett-Teller models. Sorption decreased with increasing pH, which can be explained by physisorption on the negatively charged PET surfaces and the greater presence of neutral or negatively charged MeHg species at higher pH. We used the parameters obtained by the model fits to predict the likely concentration of MeHg on PET microplastic fibers in aquatic ecosystems with environmentally realistic MeHg concentrations. We calculated MeHg concentrations on PET microplastic fibers to be four orders of magnitude lower than previously observed concentrations of MeHg in seston (suspended particles comprising algae and bacteria) at the base of the aquatic food web. The results indicate that the presence of PET microplastic fibers in the environment do not elevate the MeHg exposure to organisms that ingest fibers in the environment.

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