Photocatalytic Degradation of Selected Organophosphorus Pesticides Using Titanium Dioxide and UV Light

Abstract

The photocatalytic degradation of five selected organophosphorus pesticides (OPPs), azinphos methyl, azinphos ethyl, disulfoton, dimethoate, and fenthion, has been investigated using TiO2 (photocatalyst) and UV irradiation. The addition of H2O2 (oxidant agent) into the illuminated aquatic suspensions was also surveyed. The degradation kinetics was studied under different experimental conditions such as pesticides’ and catalyst’s concentration. Experiments were performed in a Pyrex UV laboratory-constructed photoreactor equipped with 4 × 18 W low-pressure Hg lamps emitting at 365 nm (maximum intensity 14.5 mW cm−2 at distance 15 cm). The concentration of pesticides was determined by GC-NPD means. The extent of pesticide mineralization was assessed through TOC measurements. The results demonstrated that photolysis of target organophosphates in the absence of catalyst or oxidant is a slow process resulting in incomplete mineralization. Contradictory, studied pollutants were effectively degraded in the presence of TiO2; evolution of inorganic heteroatoms (SO4 2−, PO4 3−, NO2 −, NO3 −, and NH4 +) as final products provided evidence that pesticide deterioration occurred. The photolysis efficiencies decreased in the order: disulfoton > azinphos ethyl > azinphos methyl > fenthion > dimethoate. Furthermore, a synergistic effect was observed with the addition of H2O2 in the pesticide-TiO2 suspensions. In all cases examined, reduction process appeared to follow pseudo first-order kinetics (Langmuir-Hinshelwood model). In conclusion, both catalytic systems investigated (UV-TiO2 and UV-TiO2-H2O2) have good potential for small-scale applications.