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Leaching kinetics and bioaccumulation potential of additive-derived organophosphate esters in microplastics

Environmental Pollution 2024 9 citations ? Citation count from OpenAlex, updated daily. May differ slightly from the publisher's own count. Score: 45 ? 0–100 AI score estimating relevance to the microplastics field. Papers below 30 are filtered from public browse.
Bingbing Sun, Chang Zhou, Ming Zhu, Siqi Wang, Liuyi Zhang, Chuan Yi, Chuan Yi, Haibo Ling, Mingdeng Xiang, Mingdeng Xiang, Yunjiang Yu

Summary

Researchers studied the leaching kinetics of organophosphate ester additives from microplastics in aquatic environments, finding that these flame retardants and plasticizers are released at rates that depend on temperature and water chemistry, with implications for bioaccumulation in aquatic organisms.

Polymers
Study Type Environmental

Considerable research has been conducted to evaluate microplastics (MPs) as vehicles for the transfer of hazardous pollutants in organisms. However, little effort has been devoted to the chemical release of hazardous additive-derived pollutants from MPs in gut simulations. This study looked at the leaching kinetics of organophosphate esters (OPFRs) from polypropylene (PP) and polystyrene (PS) MPs in the presence of gut surfactants, specifically sodium taurocholate, at two biologically relevant temperatures for marine organisms. Diffusion coefficients of OPFRs ranged from 1.71 × 10 to 4.04 × 10 m s in PP and 2.91 × 10 to 1.51 × 10 m s in PS. The accumulation factors for OPFRs in biota-plastic and biota-sediment interactions ranged from 1.52 × 10-69.1 and 0.02-0.7, respectively. Based on B3LYP/6-31G (d,p) calculations, the biodynamic model analysis revealed a slight increase in the bioaccumulation of OPFRs at a minor dose of 0.05% MPs. However, at higher concentrations (0.5% and 5% MPs), there was a decrease in bioaccumulation compared to the lower concentration for most OPFR compounds. In general, the ingestion of PE MPs notably contributed to the bioaccumulation of OPFRs in lugworms, whereas the contribution of PP and PS MPs was minimal. This could vary among sites exhibiting varying levels of MP concentrations or MPs displaying stronger affinities towards chemicals.

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