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Impact of CeO2 nanoparticles on the aggregation kinetics and stability of polystyrene nanoplastics: Importance of surface functionalization and solution chemistry

Water Research 2020 108 citations

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Researchers used time-resolved dynamic light scattering to investigate how cerium dioxide nanoparticles influence the aggregation and stability of differently surface-functionalized polystyrene nanoplastics across multiple water chemistries. Results showed that CeO2 nanoparticles promoted heteroaggregation with nanoplastics, with natural organic matter and ionic strength modulating aggregate formation and the environmental mobility of nanoplastics.

Polymers

The increasing application of plastics is accompanied by increasing concern over the stability and potential risk of nanoplastics. Heteroaggregation with metal-based nanoparticles (e.g., CeO-NPs) is critical to the environmental mobility of nanoplastics, as they are likely to be jointly emitted to the aquatic environment. Here, time-resolved dynamic light scattering was employed to evaluate the influence of CeO-NPs on the aggregation kinetics of differentially surface functionalized polystyrene nanoplastics (PS-NPs) in various water types. Natural organic matters and ionic strength were dominating factors influencing the heteroaggregation of PS-NPs and CeO-NPs in surface waters. The critical coagulation concentrations of PS-NPs were dependent on their surface coatings, which decreased in the presence of CeO-NPs due to electrostatic attraction and/or specific adsorption. Incubation of PS-NPs and CeO-NPs under different pH confirmed the importance of electrostatic force in the aggregation of PS NPs. A relatively low humic acid (HA) concentration promoted the heteroaggregation of NH-coated PS-NPs and CeO-NPs because the introduction of a HA surface coating decreased the electrostatic hindrance. At high HA concentrations, the aggregation was inhibited by steric repulsion. The combined effects of high efficiency of double layer compression, bridging and complexation contributed to the high capacity of Ca in destabilizing the particles. These findings demonstrate that the environmental behavior of nanoplastics is influenced by the presence of other non-plastic particles and improve our understanding of the interactions between PS-NPs and CeO-NPs in complex and realistic aqueous environments.

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