Ozonation/UV irradiation of dispersed Ag/AgI nanoparticles in water resources: stability and aggregation.

Abstract

Proliferation of nanoparticles (NPs) as aqueous pollutants is a matter of growing concern today. The aggregation kinetics of colloidal bare silver (Ag, 20.5nm) and silver iodide (AgI, 15.3nm) NPs were investigated during ozone/ultraviolet (O3/UV) oxidation. Dynamic light scattering was applied to monitor the aggregation of NPs, and the z-average of treated samples was considered aggregate diameter. The effect of temperature, pH, and initial concentration of NPs was investigated on the aggregation rate constant and stability ratio. At a short oxidation period of approximately 1min, the lower stability ratio was achieved for Ag NPs (< 50) than AgI NPs (> 100). Under acidic conditions, the negative surface charge of both NPs was neutralized that resulted in faster aggregation. In contrast, the impact of temperature and initial concentration of NPs on the aggregation rate was different for both NPs, which was due to the type of O3/UV interaction with the surface of NPs and the thickness of the electrical double layer surrounding the NPs. The aggregation behavior of Ag NPs obeyed diffusion-limited regime, while an intermediate regime between diffusion- and reaction-limited was observed for AgI NP aggregation. The resulting aggregate morphologies showed that the clusters were ramified for Ag and compressed for AgI NPs. Applying the O3/UV oxidation process for water treatment purposes leads to a significant reduction in aggregation time for inherently unstable Ag and stable AgI toxic NPs from several hours or days to several minutes.