Photocatalytic degradation of a phenylurea, chlortoluron, in water using an industrial titanium dioxide coated media

The degradation of an herbicide, chlortoluron, by UV/TiO₂ photocatalysis in water using industrial titanium dioxide coated non-woven paper was studied. The influence of parameters such as adsorption capacity, initial concentration and TiO₂ implementation (coated or in suspension) was investigated. The results emphasize the importance of operational conditions and reactor geometry on the kinetic degradation rate. The analysis of the first organic by-products suggests that a hydroxyl radical attack occurs on the phenyl ring and methyl groups of the chlortoluron before the opening of the aromatic ring. The fate of hetero-atoms has been investigated. The fates of the two nitrogen atoms in the molecule are different, not only did it depend on their initial oxidation degree, as both had the same oxidation degree, but also on the initial oxidation state of neighboring carbons. The chlorine atoms were completely released as chloride ions. The study of the influence of the oxygen concentration showed the importance of the oxygen mass transfer when designing an industrial photocatalytic reactor. An original calculation process was carried out to evaluate the adsorption constant of oxygen over the whole photocatalysis period and not only in the initial conditions as previously provided. This work points out the necessity of extending the understanding of the efficiency of chlortoluron removal or of the removal of various complex pesticide mixtures found in agricultural wastewater, using alternative, more industrially realistic, reactors.