clothianidin and titanium-dioxide

Clothianidin served as the model pollutant to investigate the performance and mechanism of pollutant removal by dielectric barrier discharge plasma (DBD) combined with the titanium dioxide-reduced graphene oxide (rGO-TiO

Topics: Catalysis; Graphite; Guanidines; Neonicotinoids; Thiazoles; Titanium

This research focused on photocatalytic degradation of imidacloprid, thiamethoxam and clothianidin employing a tailor-made photoreactor with six polychromatic fluorescent UVA (broad maximum at 355 nm) lamps and immobilised titanium dioxide (TiO(2)) on glass slides. The disappearance was followed by high pressure liquid chromatography (HPLC-DAD) analyses, wherein the efficiency of mineralization was monitored by measurements of total organic carbon (TOC). Within 2h of photocatalysis, all three neonicotinoids were degraded following first order kinetics with rate constants k=0.035 ± 0.001 min(-1) for imidacloprid, k=0.019 ± 0.001 min(-1) for thiamethoxam and k=0.021 ± 0.000 min(-1) for clothianidin. However, the rate of mineralization was low, i.e. 19.1 ± 0.2% for imidacloprid, 14.4 ± 2.9% for thiamethoxam and 14.1 ± 0.4% for clothianidin. This indicates that several transformation products were formed instead. Some of them were observed within HPLC-DAD analyses and structures were proposed according to the liquid chromatography-electro spray ionization tandem mass spectrometry analyses (LC-ESI-MS/MS). The formation of clothianidin, as thiamethoxam transformation product, was reported for the first time.

Topics: Catalysis; Chromatography, High Pressure Liquid; Chromatography, Liquid; Guanidines; Imidazoles; Insecticides; Kinetics; Neonicotinoids; Nitro Compounds; Oxazines; Photolysis; Tandem Mass Spectrometry; Thiamethoxam; Thiazoles; Titanium