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Aggregation kinetics of fragmental PET nanoplastics in aqueous environment: Complex roles of electrolytes, pH and humic acid
Summary
Researchers investigated the aggregation kinetics of fragmental PET nanoplastics under varying electrolyte concentrations, pH, and humic acid conditions, finding that aggregation increased with higher electrolyte concentrations and lower pH. Divalent cations caused stronger aggregation than monovalent cations at equal concentrations, and humic acid significantly inhibited aggregation, highlighting how natural water chemistry governs nanoplastic fate.
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. Ca and Mg) 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 CaCl and 2.0 mM MgCl, which increased to 110.4 mM NaCl and 5.6 mM CaCl 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 CaCl (1 mg L 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.