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TiO2 is the most commonly used photocatalyst in water treatment. The particle size of TiO2 is an important factor that significantly influences its activity during photocatalytic degradation. In the presence of liquid, the properties of nanopowders composed of exactly the same product clearly differ according to their aggregation size. In this study, TiO2 nanoparticles with a controlled size were fabricated by focused ultrasound dispersion. The high energy generated by this system was used to control the size of TiO2 particles in the suspension. The constant high energy released by cavitation enabled the dispersion of the particles without a surfactant. The activities of the prepared TiO2 photocatalysts for methylene blue (MB) degradation were then compared. The dye degradation effect of the photocatalyst was as high as 61.7% after 10 min when the size of the powder was controlled in the solution, but it was only as high as 41.0% when the aggregation size was not controlled. Furthermore, when the TiO2 concentration exceeded a certain level, the photocatalytic activity of TiO2 decreased. Controlling the size of the aggregated photocatalyst particles is, therefore, essential in water-treatment technologies utilizing TiO2 photocatalytic properties, and adjusting the TiO2 concentration is an important economic factor in this photocatalytic technology. This study contributes to the development of processes for degrading dyes, such as MB, released from wastewater into aquatic environments.

Titanium dioxide (TiO2) nanoparticles are used in a wide variety of products, such as renewable energy resources, cosmetics, foods, packaging materials, and inks. However, large quantities of surfactants are used to prepare waterborne TiO2 nanoparticles with long-term dispersion stability, and very few studies have investigated the development of pure water dispersion technology without the use of surfactants and synthetic auxiliaries. This study investigated the use of focused ultrasound to prepare surfactant-free waterborne TiO2 nanoparticles to determine the optimal conditions for dispersion of TiO2 nanoparticles in water. Under 395–400 kHz and 100–105 W conditions, 1 wt% TiO2 colloids were prepared. Even in the absence of a surfactant, in the water dispersion state, the nanoparticles were dispersed with a particle size distribution of ≤100 nm and did not re-agglomerate for up to 30 days, demonstrating their excellent dispersion stability.

Titanium dioxide nanoparticles (TiO2 NPs) have wide commercial applications, owing to their small size, however, the biosafety of TiO2 NPs should be evaluated further. In this study, we aimed to investigate the cytotoxicity of TiO2 NPs in the presence and absence of ultraviolet A (UVA) irradiation in human keratinocyte HaCaT cells. TiO2 NPs did not significantly affect cell viability in the absence of UVA irradiation. Nonetheless, UVA-irradiated TiO2 NPs induced caspase-dependent apoptosis of HaCaT cells. Exposure of HaCaT cells to TiO2 NPs and UVA resulted in reactive oxygen species (ROS) generation and lysosomal membrane permeabilization (LMP), both effects were not observed in the absence of UVA irradiation. An analysis of the relationship between LMP and ROS, using CA-074 as a cathepsin inhibitor or NAC as an antioxidant, showed that LMP stimulates ROS generation under these conditions. These results imply that LMP-dependent oxidative stress plays a critical role in the UVA phototoxicity of TiO2 NPs in HaCaT cells.