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The photocatalytic degradation of Salmonella choleraesuis subsp. and Vibrio parahaemolyticus in water by TiO2 catalysts was investigated in a batch reactor. After 30 min of irradiation with UV light in the presence of 1 mg/ml of TiO2, death ratio of S. choleraesuis subsp. and V. parahaemolyticus was 60% and 83%, respectively. And complete killing of the cells was achieved after 3 h of illumination in the presence of TiO2. We established the response surface methodology to investigate the effect of principal parameters on the pathogenic bacteria sterilization such as TiO2 concentration, pH and temperature. By applying response surface analysis to the bactericidal effect of S. almonella choleraesuis subsp. and V. parahaemolyticus, we found that the cell death ratio was influenced significantly by the first order term of TiO2 concentration.

In this work, the bactericidal effect of TiO2 on selected typical food pathogenic bacteria, Vibrio parahaemolyticus was studied. V. parahaemolyticus is an important pathogen of humans and aquacultured animals. We established the response surface methodology (Box-Behnken Design) to investigate the effect of principal parameters on the cell sterilization such as TiO2 concentration, UV illumination time, temperature, and pH. The sterilization rate reached maximum value at the TiO2 concentration of 1.0 mg/ml. During irradiation under the time of 30 min with UV light with the 1g-TiO2/l, the sterilization rate was greater than 85%, and 99% or more cell lost their viability with 3 hours of irradiation. Sterilization rate of the cell increased with decrease in the pH and temperature.

In this work, the bactericidal effect of TiO2 on selected typical food pathogenic bacteria, Vibrio parahaemolyticus was studied. V parahaemolyticus is an important pathogen of humans and aqua-cultured animals. We established the response surface methodology (Box-Behnken Design) to investigate the effect of principal parameters on the cell sterilization such as TiO2 concentration, UV illumination time, temperature, and pH. The sterilization rate reached maximum value at the TiO2 concentration of 1.0 mg/ml. During irradiation under the time of 30 min with UV light with the 1g-TiO2/l, the sterilization rate was greater than 85%, and 99% or more cell lost their viability with 3 hours of irradiation. Sterilization rate of the cell increased with decrease in the pH and temperature.