Heterogeneous photocatalytic degradation of phenanthrene in surfactant solution containing TiO2 particles

Photocatalytic degradation of phenanthrene (PHE) over TiO(2) in aqueous solution containing nonionic surfactant micelles was investigated. All photocatalytic experiments were conducted using a 253.7 nm mercury monochromatic ultraviolet lamp in a photocatalytic reactor. The surfactant micelles could provide a nonaqueous "cage" to result in a higher degradation rate of PHE than in an aqueous solution, but the higher Triton X-100 concentration (more than 2 g/L) lowered the degradation ratio of PHE because the additional surfactant micelles hindered the movement of micelles containing PHE so as to reduce their adsorption onto titania. Pseudo-second-order kinetics was observed for the photocatalytic degradation of PHE. Alkaline solution environment was beneficial to the photocatalytic degradation of PHE. PHE degradation could mainly be attributed to the formation of hydroxyl radicals as evident from the comparison of degradation efficiencies when O(2), H(2)O(2) and tert-butyl alcohol (TBA) were applied as oxidants or hydroxyl radical scavenger. Based on the GC/MS analysis of the intermediates, the possible pathways of the photocatalytic degradation of PHE were proposed.