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Co-photoaging inhibited the heteroaggregation between polystyrene nanoplastics and different titanium dioxide nanoparticles
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Co-photoaging of polystyrene nanoplastics and titanium dioxide nanoparticles reduced their tendency to aggregate together in water, altering the environmental fate and potential ecological risks of both contaminants.
Heteroaggregation between nanoplastics (NPs) and titanium dioxide nanoparticles (TiONPs) determines their environmental fates and ecological risks in aquatic environments. However, the co-photoaging scenario of NPs and TiONPs, interaction mechanisms of TiONPs with (aged) NPs, as well as the dependence of their heteroaggregation on TiONPs facets remain elusive. We found the critical coagulation concentration (CCC) of polystyrene nanoplastics (PSNPs) with coexisting RTiONPs was 1.9 - 2.2 times larger than that with coexisting ATiONPs, suggesting a better suspension stability of PSNPs+RTiONPs. In addition, CCC of TiONPs with coexisting photoaged PSNPs (APSNPs) was larger 1.7 - 2.2 times than that with PSNPs coexisting, indicating photoaging inhibited their heteroaggregation due to increasing electrostatic repulsion derived from increased negative charges on APSNPs and the polymer-derived dissolved organic carbon. Coexisted TiONPs promoted oxidation of PSNPs with the action of HO· and O under UV light, leading to inhibited heteroaggregation. Moreover, Van der Waals and Lewis-acid interaction dominated the formation of primary heteroaggregates of PSNPs-TiONPs (E = ‒2.20 ∼ ‒2.78 eV) and APSNPs-TiONPs (E = ‒3.29 ∼ ‒3.67 eV), respectively. The findings provide a mechanistic insight into the environmental process of NPs and TiONPs, and are significant for better understanding their environmental risks in aquatic environments.
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Photoaging-induced variations in heteroaggregation of nanoplastics and suspended sediments in aquatic environments: A case study on nanopolystyrene
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Researchers investigated how photoaging affects the aggregation behavior of polystyrene nanoplastics with suspended sediments in water. They found that 30 days of photoaging retarded aggregation in sodium chloride solutions due to steric hindrance from leached organic matter, but promoted aggregation in calcium chloride solutions through calcium bridging of newly formed oxygen-containing surface groups. The study provides mechanistic insights into how environmental weathering changes the transport and fate of nanoplastics in aquatic systems.
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Researchers found that polystyrene nanoplastics reduced the toxic effects of nano-titanium dioxide on marine algae by forming larger aggregates that decreased the bioavailability of both particle types. The combined exposure led to lower oxidative stress and reduced cellular damage compared to nano-titanium dioxide alone. The study demonstrates that interactions between different types of nanoparticles in marine environments can produce antagonistic effects that alter their individual toxicity profiles.
Influence of differently functionalized polystyrene microplastics on the toxic effects of P25 TiO2 NPs towards marine algae Chlorella sp.
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Differently functionalized polystyrene microplastics (plain, amino, carboxyl) were tested for their influence on the toxicity of TiO₂ nanoparticles to marine algae Chlorella sp., finding that microplastics altered TiO₂ aggregation behavior and modified its effective toxicity in a surface-chemistry-dependent manner. The study demonstrates that microplastic-nanoparticle interactions in marine environments can change the ecotoxicological outcome of either contaminant alone.
Combined effects of photoaging and natural organic matter on the colloidal stability of nanoplastics in aquatic environments
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Researchers found that photoaging of polystyrene nanoplastics alters how natural organic matter interacts with their surfaces — reducing humic acid adsorption while increasing protein adsorption — with downstream effects on the nanoplastics' stability and transport in aquatic environments.
Impact of CeO2 nanoparticles on the aggregation kinetics and stability of polystyrene nanoplastics: Importance of surface functionalization and solution chemistry
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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.
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