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Occurrence and sorption behaviour of bisphenols and benzophenone UV-filters in e-waste plastic and vehicle fluff

Journal of Hazardous Materials 2021 14 citations ? Citation count from OpenAlex, updated daily. May differ slightly from the publisher's own count. Score: 35 ? 0–100 AI score estimating relevance to the microplastics field. Papers below 30 are filtered from public browse.
Hans Peter H. Arp Gabriela Castro, Kristin Runde, Hans Peter H. Arp Kristin Runde, Hans Peter H. Arp Hans Peter H. Arp Hans Peter H. Arp Hans Peter H. Arp Gabriela Castro, Gabriela Castro, Hans Peter H. Arp Hans Peter H. Arp Kristine Vike-Jonas, Hans Peter H. Arp Hans Peter H. Arp Hans Peter H. Arp Gabriela Castro, Susana Villa González, Hans Peter H. Arp Hans Peter H. Arp Hans Peter H. Arp Hans Peter H. Arp Alexandros G. Asimakopoulos, Kristine Vike-Jonas, Hans Peter H. Arp Hans Peter H. Arp Gabriela Castro, Alexandros G. Asimakopoulos, Hans Peter H. Arp Alexandros G. Asimakopoulos, Hans Peter H. Arp Susana Villa González, Susana Villa González, Hans Peter H. Arp Hans Peter H. Arp Hans Peter H. Arp Alexandros G. Asimakopoulos, Alexandros G. Asimakopoulos, Hans Peter H. Arp Hans Peter H. Arp Hans Peter H. Arp Hans Peter H. Arp Alexandros G. Asimakopoulos, Hans Peter H. Arp Hans Peter H. Arp Hans Peter H. Arp Hans Peter H. Arp

Summary

This study measured bisphenols and benzophenone UV-filter chemicals in e-waste plastics and shredded vehicle materials. Both types of plastic waste contained multiple hazardous chemicals that could leach into the environment during disposal or recycling. The findings highlight the chemical contamination risks associated with plastic waste from electronics and end-of-life vehicles.

Bisphenols and benzophenone UV-filters are hazardous, high production volume chemicals. There is concern that these contaminants could leach into the environment or be recycled into new products during waste management. To investigate this, nine bisphenols and five benzophenones were quantified in Norwegian e-waste and car fluff. To understand their leachability, equilibrium passive sampling methodology, using polyoxymethylene (POM), was calibrated for these substances, many of which for the first time. This method can differentiate freely dissolved substances in the aqueous phase from those sorbed to suspended colloids and microplastics in the leachate water. Equilibrium POM partitioning was reached within 14 days of shaking; all bisphenols and benzophenone UV-filters exhibited linear isotherms (R<sup>2</sup> ranged from 0.83 to 1.0), when deriving POM-water partition coefficients (K<sub>POM</sub>). Bisphenol A and bisphenol F displayed the highest concentrations, with maximum levels of 246,000 and 42,400 ng g<sup>-1</sup>, respectively. Logarithms of waste-water partition coefficients (log K<sub>waste</sub>) ranged from 1.7 (benzophenone 2) to 4.5 (bisphenol P). The established K<sub>POM</sub> values agreed with measured K<sub>waste</sub> values (within a factor of ~3), unlike octanol-water partition coefficients. This indicated that POM is a better surrogate for waste plastic partitioning than octanol. Results are discussed in the context of assessing risks from waste management in a circular economy.

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