Degradation of carbofuran in aqueous solution by Fe(III) aquacomplexes as effective photocatalysts

The photodegradation of carbofuran by excitation of iron(III) aquacomplexes was investigated under UV irradiation. The degradation rate was strongly influenced by the pH, and initial concentration of Fe(III). The degradation efficiency of carbofuran at the difference pH was in good agreement with the initial concentration of Fe(OH)2+ in the solution. An initial carbofuran concentration of 10 mg L−1 was completely degraded within 50 min at pH 2.8 with original Fe(III) concentration of 8 × 10−4 mol L−1. This degradation reaction was found to follow the first order kinetics law and the rate constant of 1.60 × 10−3 s−1 was observed. The decrease of TOC content was observed during the photocatalytic process and the removal percentage obtained was about 70% after 25 h. Furthermore, ammonium ion as an end-product was detected in the solution. Therefore, this process based on the catalytic reaction of Fe(II, III) is responsible for the continuous production of hydroxyl radicals in such system. A gas chromatography-mass spectrometry analysis showed the formation of four photoproducts, such as 2,2-dimethyl-2,3-dihydro-benzofuran-7-ol, etc., revealing that the carbamate branch, C-3 and C-2 positions in furan ring were attack targets of hydroxyl radicals. Based on these results, the photocatalytic system could be useful technology for the treatment and the mineralization of compounds like carbofuran.