Aggregation kinetics of fragmental PET nanoplastics in aqueous environment: Complex roles of electrolytes, pH and humic acid

The aggregation kinetics of fragmental polyethylene glycol terephthalate (PET) nanoplastics under various chemistry conditions in aqueous environment were firstly investigated in this work. The aggregation of PET nanoplastics increased with increasing electrolyte concentrations and decreasing solution pH, which became stronger with the presence of divalent cations (e.g. Ca2+ and Mg2+) than that of monovalent cations (e.g. Na+ and K+). The effect of cations with the same valence on the aggregation of PET nanoplastics was similar. The measured critical coagulation concentrations (CCC) for PET nanoplastics at pH 6 were 55.0 mM KCl, 54.2 mM NaCl, 2.1 mM CaCl2 and 2.0 mM MgCl2, which increased to 110.4 mM NaCl and 5.6 mM CaCl2 at pH 10. In addition, the aggregation of PET nanoplastics was significantly inhibited with the presence of humic acid (HA), and the CCC values increased to 558.8 mM NaCl and 12.3 mM CaCl2 (1 mg L-1 HA). Results from this study showed that the fragmental PET nanoplastics had the quite higher CCC values and stability in aqueous environment. In addition, the aggregation behaviors of PET nanoplastics can be successfully predicted by the Derjguin Landau Verwey Overbeek (DLVO) theory. (C) 2020 Elsevier Ltd. All rights reserved.

Automated summary

The aggregation kinetics of fragmental polyethylene glycol terephthalate (PET) nanoplastics in aqueous environment were studied under various chemistry conditions. It was found that the aggregation of PET nanoplastics increased with higher electrolyte concentrations and lower solution pH, especially in the presence of divalent cations. Additionally, the presence of humic acid was shown to significantly inhibit the aggregation of PET nanoplastics.