Comparative activity of TiO2 microspheres and P25 powder for organic degradation: Implicative importance of structural defects and organic adsorption

Abstract TiO 2 microspheres have been employed as a promisingly new photocatalyst for water and wastewater treatment. P25 TiO 2 is commonly employed and its properties are well established as photocatalyst. In this study, photocatalytic activities of the two TiO 2 samples are compared by degrading sulfosalicylic acid (SSA), phenol, and 2,4-Dichlorophenoxyacetic acid (2,4-D) under 365 nm UV illumination in a suspension system at neutral pH and associated optimized TiO 2 dosages. The results showed that the three organic compounds unexceptionally degraded more rapidly on P25 than on TiO 2 microspheres in terms of the concentration–time curves and total organic carbon removals at 120 min. This might me attributed the presence of oxygen vacancies and Ti(III) defects already present on P25 as determined by electron paramagnetic resonance, implying that the defects played an important role for the enhancement of the charge transfer step as rate-determining step. The degradations of three organic compounds on P25 and TiO 2 microspheres could be well described by the first-order rate equation, while the degradation kinetics of SSA on TiO 2 microspheres was quite different. The difference was ascribed to the medium adsorption ability of SSA on the TiO 2 surface.