Abstract

Nanoplastics (NPs) usually coexist with impurity-bearing ferrihydrite (ImFh), and their interaction is related to their environmental fate. In this study, the aggregation between ImFh (impurities: Al, Mn and Si) and polystyrene nanoplastics (PSNPs), as well as the sedimentation of ImFh-PSNP complex particles in the aqueous phase were investigated systematically with particle concentrations of 100 mg/L ImFh and 10 mg/L PSNPs. Our results revealed that the PSNP suspension was dispersive and stable under various pH values and low ion strength. After coexisting with ImFh, PSNPs aggregated with the positively charged ImFh to form ImFh-PSNP complex particles, which destroyed the stability of PSNPs. The increase in pH and Na+ concentration could inhibit their aggregation, but high Na+ concentration (>20 mM) caused the homoaggregation of PSNPs. The aggregation capacity of PSNPs with ImFh was in the order of Al-bearing Fh > Fh > Mn-bearing Fh > Si-bearing Fh. Zeta potential and Derjaguin–Landau–Verwey–Overbeek (DLVO) calculations indicated that Al-bearing Fh showed higher positive potential than pure Fh, which caused stronger electrostatic interactions with PSNPs. However, Mn and Si in ImFh decreased the positive potential and inhibited the electrostatic interaction with PSNPs, and the effect of Si was greater than that of Mn. The aggregation between ImFh and PSNPs inhibited the sedimentation of their complex particles, and the higher aggregation capacity appeared to have a greater inhibition degree. Due to the “electrostatic patches” effect of PSNPs, the energy barrier of the ImFh-PSNPs particles was higher than that of the ImFh particles. Our findings clarified the influence of impurities on the interaction between ImFh and PSNPs and provided insight regarding their fate in the environment.

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