Photodegradation of dimethyl phthalate (DMP) by UV-TiO2 in aqueous solution: operational parameters and kinetic analysis.

In this paper, the adsorption and degradation phenomenon involved in the photocatalytic degradation of dimethyl phthalates (DMPs) by titanium dioxide (TiO₂) was studied. A variety of operating variables were selected firstly. Then, it was proved that even for such weak adsorption properties molecules as DMP, adsorption was still an important prerequisite for photolysis. A surface-mediated reaction process was proposed that the photodegradation of DMP assisted by TiO₂ particles occurred primarily at the surface of the photocatalyst rather than in the homogeneous phase. According to Langmuir-Hinshelwood model, the adsorption constant determined from the dark adsorption was far less than that obtained in the light condition. Enhanced DMP adsorption on the surface of TiO₂ under irradiation was the possible reason for the improvement of photodegradation efficiency. Under the irradiation of light, a synergistic mechanism of adsorption and photocatalysis was responsible for DMP degradation. The quantitative analysis by adding scavengers indicated that ^·OH radical was primarily responsible for the photodegradation of DMP. It was further verified that ^·OH was produced much more from conduction band electrons rather than valance band holes toward photodegradation of DMP by adding foreign Cu²⁺. [ABSTRACT FROM AUTHOR]