A comparative study for the removal of imidacloprid insecticide from water by chemical-less UVC, UVC/TiO2 and UVC/ZnO processes

• Published in: Journal of environmental health science and engineering 2019-06, Vol.17 (1), p.337-351
• Main Authors: Yari, Khadije, Seidmohammadi, Abdolmotaleb, Khazaei, Mohammad, Bhatnagar, Amit, Leili, Mostafa
• Format: Article
• Language: English
• Subjects: Aqueous solutions; Catalysis; Comparative literature; Comparative studies; Earth and Environmental Science; Environment; Environmental Economics; Environmental Engineering/Biotechnology; Environmental Health; Environmental Law/Policy/Ecojustice; Health risks; Illumination; Imidacloprid; Insecticides; Intermediates; Kinetics; Low pressure; Mercury; Mercury lamps; Mercury vapor; Methods; Mineralization; Nanoparticles; Occupational health; Organic chemistry; Oxidation; Oxidation-reduction reactions; Pesticides; pH effects; Photocatalysis; Photodegradation; Photolysis; Public health; Quality of Life Research; Radiation (Physics); Reaction kinetics; Research Article; Sewage treatment; Titanium dioxide; Ultraviolet radiation; Waste Management/Waste Technology; Water; Zinc oxide
• ISSN: 2052-336X; 2052-336X
• DOI: 10.1007/s40201-019-00352-3

Background Chloronicotinic insecticide are a class of pesticides that are commonly used as insecticides. Among the frequently used chloronicotinic pesticide, imidacloprid (IM) was developed in 1986. The residual of this insecticide or any pesticides may have serious public health threats. Methods Both degradation and mineralization of the imidacloprid (IM) in aqueous solution was studied under various experimental conditions using different advanced oxidation processes namely, ultraviolet C (UVC), UVC + TiO 2 , and UVC + ZnO. All the experiments were performed using a lab-scale batch photoreactor with a working volume of 100 mL equipped with low-pressure mercury vapor lamp (9 W, 18 cm long, Philips Co.), emitting UV radiation with maximum intensity at 254 nm. The possible intermediates and a reaction pathway for photocatalytic degradation of the IM were also evaluated. Results It was observed that under optimal condition for UVC/TiO 2 process (C 0  = 100 mg/L, pH = 7.5, t = 20 min, TiO 2 dose = 100 mg/L), IM was effectively degraded (88.15%) and followed the first order kinetics model. The degradation efficiency increased with increasing of illumination time and is more favorable in alkaline pH compared to acidic pH. Degradation of the IM in photocatalytic process was compared with photolysis showing a significant synergy effect in the case of the photocatalytic degradation process, leading at 20 min illumination time to a 36.7% increase of the IM removal efficiency in comparison to the single UVC. The GC/MS chromatograms before and after treatment confirmed the effectiveness of the UVC/TiO 2 process in simplifying the nature of IM and its conversion to more simple and degradable compounds. Conclusion The heterogeneous UVC/TiO 2 process was found to be an efficient chemical-less method that is appropriate for degradation of IM from aqueous phase.