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Development of a dispersive liquid–liquid microextraction method for the determination of plastic additives in seawater

Analytical Methods 2024 3 citations ? Citation count from OpenAlex, updated daily. May differ slightly from the publisher's own count.
María-José González-Castro, Jaime Uribe-Ares, Soledad Muniategui‐Lorenzo, E. Beceiro-González

Summary

Researchers developed a sensitive liquid-liquid microextraction method to detect seven plastic additive chemicals — including phthalates, triclosan, and antioxidants — in seawater, achieving good recovery and detection limits in the parts-per-billion range. These additives leach from microplastics into surrounding water and carry their own toxicity, meaning the chemical contamination from plastic pollution extends well beyond the physical particles themselves.

Study Type Environmental

A method using dispersive liquid-liquid microextraction (DLLME) prior to high performance liquid chromatography-diode array detection (HPLC-DAD) was developed to determine seven additives from the plastics industry (butylated hydroxytoluene, diisodecyl phthalate, irgafos 168, lawsone, quercetin, triclosan and vitamin E) in seawater samples. These compounds can reach seawater due to direct discharge from wastewater treatment plants and leaching from plastics and microplastics. The extraction was performed using 25 mL of seawater, 500 μL of 1-octanol (extraction solvent) and a stirring step instead of dispersive solvent. Additive concentrations were determined by LC-DAD on a C18 column with a mobile phase of acetonitrile and phosphoric acid aqueous solution (pH 3.5) by gradient elution. The analytical recoveries ranged from 82 to 93% for all compounds, except for lawsone (60%). Repeatability and intermediate precision were adequate with RSD < calculated values following the Horwitz equation at the concentration levels evaluated (0.06 and 0.24 mg L-1). All additives exhibited linear matrix calibration curves (R2 > 0.99). Detection limits ranged from 0.009 to 0.028 mg L-1 and quantification limits ranged from 0.027 to 0.084 mg L-1. Finally, the application of the method to real samples verified the method as accurate and applicable to seawater.

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