Sonocatalytic facilitation of hydroxyl radical generation in the presence of TiO2.

The generation of hydroxyl (OH) radicals was investigated during ultrasonic irradiation and in the presence of TiO(2). The effect of TiO(2) on an ultrasonic system's oxidation power was evaluated by examining the oxidation of salicylic acid. The generation of the salicylic acid derivatives, 2,3-dihydroxybenzoic acid (DHBA) and 2,5-DHBA, was measured by high-performance liquid chromatography coupled with electrochemical detection under different experimental conditions. The presence of TiO(2) enhanced the generation of DHBA during ultrasonic irradiation, thus indicating a higher oxidation power in the ultrasonic system. Al(2)O(3) also increased the generation of DHBA during irradiation; however, the effect of TiO(2) was found to be higher than that of Al(2)O(3). The addition of OH radical scavengers such as dimethylsulfoxide (DMSO), methanol and mannitol significantly suppressed the production of DHBA, and DMSO was found to have the highest suppressive effect among all scavengers. The effects of dissolved gases on the generation of OH radicals were further studied, and their power was found to be in the order Xe > Ar > O(2) > N(2). The degassing of the irradiation solution completely suppressed the generation of OH radicals. These results indicate that the presence of TiO(2) accelerates the generation of OH radicals during ultrasonic irradiation, and that the process may be mediated through the induction of cavitation bubbles in irradiating solutions.

Decolorization of methylene blue in aqueous suspensions of titanium peroxide.

The pretreatment of TiO(2)-photocatalysts in solutions of H(2)O(2) was studied by examining the decolorization of methylene blue in the dark. Incubation of TiO(2) particles in H(2)O(2) solutions increased the oxidizing capacity of TiO(2). Methylene blue (0.3 mM) was degraded in the presence of pretreated TiO(2), and a decolorizing ratio of 47% was obtained after a 48-h incubation period in the presence of 5.0 g/L pretreated TiO(2). Titanium peroxide as a stable oxidant, which can be synthesized with the reaction of titanium sulfate and H(2)O(2), was studied in the decolorizing process of methylene blue. Concentrations of methylene blue were significantly reduced in the presence of titanium peroxide, and a greater extent of decolorization was obtained with larger amounts of titanium peroxide. A 63% decrease in methylene blue concentration was achieved in 5h incubation in the presence of 4.0 g/L titanium peroxide. H(2)O(2) accelerated the decolorizing process in the presence of titanium peroxide. The addition of 100 mM H(2)O(2) to a methylene blue solution containing 2.0 g/L titanium peroxide increased the decolorizing ratio to 85% after 5 h incubation. The addition of a hydroxyl radical scavenger, dimethyl sulfoxide, significantly decreased the decolorizing ratio, indicating the role of hydroxyl radicals in the oxidation process.

Sonocatalytic degradation of methylene blue with TiO2 pellets in water.

A series of experiments were carried out to study the degradation of methylene blue by the irradiation of ultrasound onto TiO(2) in aqueous solution. A statistically significant decrease in the concentration of methylene blue was observed after 60 min irradiation. While the reduction was 22% of the initial concentration without H(2)O(2), addition of H(2)O(2) significantly enhanced the degradation of methylene blue for the TiO(2) containing system (85% reduction of the initial concentration). The addition of H(2)O(2) had no effect on the methylene blue degradation when the system contained Al(2)O(3). The degradation ratio of methylene blue was dependent on the amount of TiO(2) and also the specific surface area of TiO(2) in the solution. The effects of radical scavenging agents on the degradation of methylene blue were also investigated for the system with TiO(2). It was found that the radical scavenging agents dimethyl sulfoxide (DMSO), methanol, and mannitol suppressed the degradation, with DMSO being the most effective. The effect of pH on the degradation of methylene blue was further investigated. An U-shaped change in the concentration of methylene blue in the presence of TiO(2) was observed along with the change in pH values (pH 3-12), and the highest degradation ratio was observed at around pH 7. In conclusion, ultrasound irradiation of TiO(2) in aqueous solution resulted in significant generation of hydroxyl radicals, and this process may have potential for the treatment of organic dyes in wastewater.

Disinfection of Legionella pneumophila by ultrasonic treatment with TiO2.

An ultrasonic treatment system, using a TiO2 photocatalyst, was used to disinfect Legionella pneumophila. A kinetic study of the process indicates that TiO2 significantly improves the disinfection process. The concentrations of viable cells were reduced to 6% of the initial concentrations in the presence of 0.2g/ml TiO2 after a 30 min of treatment period, while only an 18% reduction was observed in the absence of TiO2 . The potency of the disinfection could be enhanced, to some extent, by increasing the amount of TiO2 used. Cell concentrations were decreased by an order of 3 within 30 min of treatment in the presence of 1.0 g/ml TiO2 . The disinfection power in the presence of TiO2 versus Al2O3 was also compared and the findings showed that TiO2 induced a higher cell killing. No significant effect of initial cell concentration on the disinfection was found in the range of 10(2)-10(7) CFU/ml after a 30 min of treatment period. The mechanism of cell killing was investigated by examining the effects of OH radical scavengers such as ascorbic acid, histidine and glutathione. The disinfection power was reduced in samples that contained these radical scavengers, thus indicating the importance of OH radicals.