Photodegradation of 2,4-D induced by NO2- in aqueous solutions：The role of NO2
Chunyan Yu , Hua Wang , Xuan Liu , Xie Quan
,
Shuo Chen
,
Jianlin Zhang
,
Peng Zhang
DOI:10.1016/j.jes.2014.05.002
Received August 26, 2013,Revised November 22, 2013, Accepted , Available online July 09, 2014
Volume 26,2014,Pages 1383-1388
To elucidate the effect of nitrite ion (NO2-) on the photodegradation of organic pollutants, a 300 W mercury lamp and Pyrex tubes restricting the transmission of wavelengths below 290 nm were used to simulate sunlight, and the photodegradation processes of 2,4-dichlorophenoxyacetic acid (2,4-D) with different concentrations of NO2- in freshwater and seawater were studied. The effect of reactive oxygen species (ROS) on the photolysis of 2,4-D was also demonstrated using electron paramagnetic resonance (EPR). The results indicated that the 2,4-D photolysis reaction followed the first-order kinetics in freshwater and seawater under different concentrations of NO2-. Meanwhile, the photochemical reaction rate of 2,4-D increased with increasing concentration of NO2-. When the concentration of NO2- was lower than 23 mg/L, the photodegradation rate of 2,4-D in seawater was higher than that in freshwater. However, when the concentration of NO2- was reached 230 mg/L, 2,4-D degradation slowed down in seawater. It was important to note that EPR spectra showed NO2 U radical was generated in theNO2- solution under simulated sunlight irradiation, indicating that 2,4-D photodegradation could be induced by NO2 U. These results show the key role of NO2- in photochemistry and are helpful for better understanding of the phototransformation of environmental contaminants in natural aquatic systems.
