An insight into aggregation kinetics of polystyrene nanoplastics interaction with metal cations

Once inevitably released into the aquatic environment, polystyrene nanoplastics (PS-NPs) will present complicated environmental behaviors, of which the aggregation is a key process determining their environmental fate and impact. In this study, the aggregation kinetics of different sizes (30 nm and 100 nm) of PS-NPs with metal cations (Na + , K + , Ca 2+ , Mg 2+ and Pb 2+ ) at different solution pH (3, 6 and 8) were investigated. The results showed that the aggregation of PS-NPs increased with cation concentration. Taking Pb 2+ as an example, the adsorption behavior of cations onto PS-NPs was determined by transmission electron microscopy (TEM) and energy dispersive X-ray (EDX) spectroscopy, which demonstrated Pb 2+ could be adhered onto the surface of PS-NPs with the effect of charge neutralization. The critical coagulation concentrations (CCC) of smaller PS-NPs were higher than that of larger PS-NPs for monovalent cations, whereas a different pattern is observed for divalent cations. It was suggested that there were other factors that DLVO theory does not consider affect the stability of NPs with different particle sizes. In addition, it should be noted that PS-NPs had the capacity of adsorbing large amounts of heavy metal cations and carried them transport to a long distance, and the corresponding ecological risks need to further elucidate. The aggregation kinetics of different sizes of polystyrene nanoplastics with metal cations at different solution pH were investigated. The adsorption behavior of cations onto nanoplastics was determined by TEM and EDX, which demonstrated the adherence of cations onto the surface of nanoplastics with the effect of charge neutralization.