[Degradation of Triphenyl Phosphate in Water by UV-driven Advanced Oxidation Processes].

Abstract

As a type of emerging pollutant of concern, organophosphate esters (OPEs) have posed a moderate risk to the remote Antarctic waters. Triphenyl phosphate (TPHP) is a common type of OPEs in water, which has been proven to have toxic effects, bioaccumulation, and amplification effects and pose a great threat to the environment and human health. Fourier transform infrared spectroscopy (FT-IR) and liquid chromatography-tandem mass spectrometry (LC-MS/MS) were used to investigate the degradation process of TPHP in three advanced oxidation processes (UV-AOPs), including ultraviolet-hydrogen peroxide (UV-H₂O₂), ultraviolet-titanium dioxide (UV-TiO₂), and ultraviolet-persulfate (UV-PS) systems. This was the first instance of using FT-IR for the online observation of the change in infrared characteristic peaks in the degradation process of TPHP, and its degradation reaction kinetics, photodegradation products, and degradation pathways were analyzed. The results showed that TPHP could be effectively degraded under UV-H₂O₂, UV-TiO₂, and UV-PS systems, and the photodegradation half-lives were 74, 150, and 89 min, respectively. The UV-H₂O₂ system had the best degradation effect on TPHP. Additionally, the degradation reactions of TPHP in three systems conformed to the first-order kinetics. When the concentration of H₂O₂ was 0-0.097 mol·L^-1, the increase in H₂O₂ concentration promoted the degradation of TPHP, and when the concentration of TiO₂ was 0-0.013 mol·L^-1, the increase in TiO₂ concentration promoted the degradation of TPHP. The photodegradation pathway of TPHP mainly included the P-O-C bond breaking, the C-H bond cleavage of the benzene ring structure and the hydrolysis reaction of TPHP. The UV-H₂O₂ system was used to degrade OPEs in the environmental water of Chengdu, and it was found that the removal rate of TPHP was 66% when the water samples of the park landscape water were degraded for 60 min.