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+.