| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 4410362 | Chemosphere | 2011 | 6 Pages |
Photolysis of Enro in water was investigated under simulated sunlight irradiation using a Xenon lamp. The results showed that Enro photolysis followed apparent first-order kinetics. Increasing Enro concentration from 5.0 to 40.0 mg L−1 led to the decrease of the photolysis rate constant from 1.6 × 10−2 to 3.0 × 10−3 min−1. Compared with the acidic and basic conditions, the photolysis rate was faster at neutral condition. Both of nitrate and humic acid can markedly decrease the photolysis rate of Enro because they can competitively absorb photons with Enro. The electron spin resonance and reactive oxygen species scavenging experiments indicated that Enro underwent self-sensitized photooxidation via OH and 1O2. After irradiation for 90 min, only 13.1% reduction of TOC occurred in spite of fast photolysis of 58.9% of Enro, indicating that Enro was transformed into intermediates without complete mineralization. The photolysis of Enro involved three main pathways: decarboxylation, defluorination, and piperazinyl N4-dealkylation. The bioluminescence inhibition rate using Vibrio fischeri increased to 67.2% at 60 min and then decreased to 56.9% at 90 min, indicative of the generation of some more toxic intermediates than Enro and then the degradation of the intermediates. The results will help us understand fundamental mechanisms of Enro photolysis and provide insight into the potential fate and transformation of Enro in surface waters.
► Both of nitrate and humic acid can markedly decrease the photolysis rate of Enro. ► Enro undergoes both direct and self-sensitized photolysis via OH and 1O2. ► The photolysis of Enro involves three main pathways. ► Photolysis of Enro reduces the toxicity to the environment ecosystem function.
