New Route to Toxic Nitro and Nitroso Products upon Irradiation of Micropollutant Mixtures Containing Imidacloprid: Role of NOx and Effect of Natural Organic Matter

Abstract

In this study, we reveal the capacity of imidacloprid (a neonicotinoid insecticide) to photoinduce the nitration and nitrosation of three aromatic probes (phenol, resorcinol, and tryptophan) in water. Using a gas-flow reactor and a NOx analyzer, the production of gaseous NO/NO2 was demonstrated during irradiation (300-450 nm) of imidacloprid (10-4 M). Quantum calculations showed that the formation of NOx proceeds via homolytic cleavage of the RN-NO2 bond in the triplet state. In addition to gaseous NO/NO2, nitrite and nitrate were also detected in water, with the following mass balance: 40 ± 8% for NO2, 2 ± 0.5% for NO, 52 ± 5% for NO3-, and 16 ± 2% for NO2-. The formation of nitro/nitroso probe derivatives was evidenced by high-resolution mass spectrometry, and their yields were found to range between 0.08 and 5.1%. The contribution of NO3-/NO2- to the nitration and nitrosation processes was found to be minor under our experimental conditions. In contrast, the addition of natural organic matter (NOM) significantly enhanced the yields of nitro/nitroso derivatives, likely via the production of triplet excited states (3NOM*) and HO•. These findings reveal the importance of investigating the photochemical reactivity of water contaminants in a mixture to better understand the cocktail effects on their fate and toxicity.