Solar photocatalytic degradation of total organic halogen in water using TiO2 catalyst

Disinfection byproducts (DBPs) in treated wastewater effluents pose environmental and health risks during water reuse. Solar-TiO2 photocatalysis is a promising technology for degrading organic pollutants in treated effluents. In this study, total organic halogen (TOX) was used as an analytical tool to determine the efficiency of solar-TiO2 photocatalytic process for the dehalogenation of DBPs in water. Natural solar photocatalytic experiments using TiO2 particles were conducted to evaluate dehalogenation kinetics of different TOX groups formed by fulvic acid including total organic chlorine (TOCl), bromine (TOBr) and iodine (TOI). The results showed that the mixed phase TiO2 (Aeroxide P25) was much more effective at TOX removal than the anatase (Hombikat UV-100) and rutile (TiOxide) TiO2 particles. The TOX photocatalytic degradation rates of different halogen substituents ranked as TOI > TOCl (NH2Cl) > TOBr > TOCl (Cl2). The TOX removal followed first-order kinetics with half-lives of 42.8, 11.0, 5.0 and 2.7 min for TOCl (Cl2), TOBr, TOCl (NH2Cl), and TOI, respectively, at the 100 mg L−1 TiO2 dose. The TOX dehalogenation was enhanced at pH 9 compared to pH 5, and the addition of hydrogen peroxide had limited improvement in the TOX removal. Hydrophobic and molecular weight (MW) > 1 kDa fractions of TOCl (Cl2) were more susceptible to the solar photocatalytic process than the hydrophilic and MW TOCl (NH2Cl) > TOBr > TOCl (Cl2).•Half-lives of different TOX groups by solar-TiO2 treatment: 2.7 – 42.8 min.•High molecular weight TOX degraded faster than low molecular weight TOX.