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Sorption of tetrabromobisphenol A onto microplastics: Behavior, mechanisms, and the effects of sorbent and environmental factors

Ecotoxicology and Environmental Safety 2021 77 citations ? Citation count from OpenAlex, updated daily. May differ slightly from the publisher's own count.
Shengsheng Li, Ruixue Ma, Xiaohui Zhu, Chang Liu, Liangzhong Li, Ziling Yu, Xichao Chen, Zongrui Li, Yan Yang

Summary

The sorption of the flame retardant tetrabromobisphenol-A (TBBPA) onto four types of microplastics — polyethylene, polypropylene, polystyrene, and polyvinyl chloride — was studied in aqueous environments. Results revealed that polymer type, surface area, and hydrophobic interactions were key factors controlling how much TBBPA accumulates on microplastic surfaces.

Microplastics (MPs) and halogenated organic pollutants coexist in ambient water and MPs tend to sorb organic pollutants from surrounding environments. Herein, a study on the sorption behavior of tetrabromobisphenol-A (TBBPA) onto four different MPs, namely, polyethylene (PE), polypropylene (PP), polystyrene (PS), and polyvinyl chloride (PVC) was carried out. Effects of MPs properties and environmental factors, including the type, surface charge and pore volume as well as the ionic strength (Ca2+) and humic acid (HA) on the sorption of TBBPA were discussed. Results showed that the sorption of TBBPA onto the MPs could reached an equilibrium within 24 h, and the sorption capacities decreased in the following order -PVC (101.85 mg kg-1) >PS (78.95 mg kg-1) >PP (58.57 mg kg-1) >PE (49.43 mg kg-1). Adsorption kinetics data fitted by intraparticle diffusion model revealed both surface sorption and intraparticle diffusion contributed, in the interfacial diffusion stage approximately 11-29% of TBBPA slowly diffused onto the surface of the MPs, and finally, in the intraparticle diffusion stage. The increase of Ca2+ concentration could promote the sorption of TBBPA by PE, PP, and PS, but no significant alteration for PVC. For all the four MPs, HA was found to exert a negative effect on TBBPA sorption. The adsorption was mainly driven by hydrophobic partition and electrostatic interactions.

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