Here, we assessed the heteroaggregation of polystyrene (PS) and poly(vinyl chloride) (PVC) nanoplastics with SiO2 as a model of natural colloids. Homoaggregation and heteroaggregation were evaluated as a function of CaCl2 (0-100 mM) and natural organic matter (NOM) (50 mg L-1) at a designated concentration of nanoplastics (200 μg L-1). Critical coagulation concentrations (CCC) of nanoplastics were determined in homoaggregation and heteroaggregation experiments with SiO2 and CaCl2. The attachment efficiency (α) was calculated by quantifying the number of nanoplastics in the presence of CaCl2, NOM, and SiO2 using single-particle inductively coupled plasma mass spectrometry (spICP-MS) and pseudo-first-order kinetics. The calculated α was fed into the SimpleBox4Plastics model to predict the fate of nanoplastics across air, water, soil, and sediment compartments. Nanoplastics exhibited high stability against homoaggregation, while significant heteroaggregation with SiO2 occurred at CaCl2 concentrations above 100 mM. The influence of NOM was also evaluated, showing a reduction in heteroaggregation with SiO2 for both nanoplastic types. Sensitivity analysis indicated that the degradation half-life of the tested nanoplastics had a more significant impact on persistence than did α. The results emphasize the environmental stability of nanoplastics, particularly in freshwater and soil compartments, and the critical role of NOM and emission pathways in determining their fate.

• Klíčová slova
• SimpleBox4Plastics model, freshwater, microplastics, natural organic matter, plastic fate,
• MeSH
• chemické modely MeSH
• chlorid vápenatý chemie   MeSH
• koloidy chemie   MeSH
• nanočástice MeSH
• oxid křemičitý chemie   MeSH
• polystyreny * chemie   MeSH
• polyvinylchlorid * chemie   MeSH
• Publikační typ
• časopisecké články MeSH
• Názvy látek
• chlorid vápenatý MeSH
• koloidy MeSH
• oxid křemičitý MeSH
• polystyreny * MeSH
• polyvinylchlorid * MeSH