Photodegradation of Neonicotinoid Active Ingredients and Their Commercial Formulations in Water by Different Advanced Oxidation Processes

• Published in: Water, air, and soil pollution air, and soil pollution, 2014-05, Vol.225 (5), p.1-10, Article 1954
• Main Authors: Banic, Nemanja D, Sojic, Daniela V, Krstic, Jugoslav B, Abramovic, Biljana F
• Format: Article
• Language: English
• Subjects: acetamiprid; active ingredients; Adsorption; Analysis; aqueous solutions; Atmospheric Protection/Air Quality Control/Air Pollution; Bioremediation; Calypso; Catalysts; Climate Change/Climate Change Impacts; Earth and Environmental Science; Efficiency; Environment; Environmental monitoring; Experiments; Free radicals; Hydrogen peroxide; Hydrogeology; Hydroxyl radicals; Imidacloprid; Insecticides; iron; Irradiation; Light; Mineralization; Nuclear radiation; Organic contaminants; Oxidation; Oxidation-reduction reaction; Pesticides; Photocatalysis; Photodegradation; Photolysis; Photoreduction; Pollutants; Soil contamination; Soil Science & Conservation; Studies; Thiacloprid; Thiamethoxam; Titanium dioxide; Ultraviolet radiation; Water pollution; Water Quality/Water Pollution
• ISSN: 0049-6979; 1573-2932
• DOI: 10.1007/s11270-014-1954-5

This contribution is concerned with the comparison of the efficiency of the removal of four pure neonicotinoid active ingredients (AIs) and their commercial formulations (CFs) from aqueous solutions by using different advanced oxidation processes at the pH 2.8. The AIs of thiamethoxam and imidacloprid, and their CFs (Actara and Confidor), having a nitroguanidine functional group, exhibited low persistence to photolysis. In contrast to them, thiacloprid and acetamiprid and their CFs (Calypso and Mospilan), containing a cyanoimine functional group, were stable during the UV irradiation period. As expected, the degradation rate of the studied neonicotinoids increased significantly in the combined action of UV radiation and H₂O₂. In the case of thiacloprid and acetamiprid and their CFs, the reaction of the OH radicals formed and molecules of these insecticides was the major destruction pathway. The increased photodegradation efficiency of the UV/7.2Fe/TiO₂/H₂O₂ and vis/7.2Fe/TiO₂/H₂O₂ processes was attributed to the surface photoreduction of Fe³⁺ to Fe²⁺, which produces new OH radicals in the reaction with H₂O₂. In the presence of visible light, the efficiency may be partly due to the formation of the H₂O₂–TiO₂ complexes. For the 7.2Fe/TiO₂/H₂O₂ process in the presence of UV or visible radiation, no significant influence on the efficiency of photodegradation was observed in dependence of the structural differences of selected neonicotinoids. These results strongly suggest that highly reactive hydroxyl radicals, generated on the catalyst’s surface in the reaction involving H₂O₂, are responsible for this oxidation. In order to investigate degree of mineralization for all insecticides, TOC measurements were also conducted. Also, it was observed that the removal of pure AIs and their CFs by dark adsorption was almost negligible.