Mineralization of antibiotic sulfamethoxazole by photoelectro-Fenton treatment using activated carbon fiber cathode and under UVA irradiation

摘要

The mineralization of antibiotic sulfamethoxazole (SMX) of concentrations up to 300 mg L(-1) was examined by photoelectro-Fenton (PEF) using an activated carbon fiber (ACF) cathode with UVA (365 nm) irradiation. Comparative mineralization has been studied by different methods: RuO(2)/Ti anodic oxidation (AO). AO in the presence of electrogenerated H(2)O(2) (AO-H(2)O(2)), AO-H(2)O(2) in the presence of UVA (AO-H(2)O(2)-UVA), and both the electro-Fenton (EF) and PEF processes. PEF treatment at a low applied current of 0.36 A yields a faster and more complete depollution with 80% of the TOC removed after 6 h of electrolysis. The higher oxidative ability of the PEF process can be attributed to the additional hydroxyl radicals (center dot OH) produced by the photo-Fenton reaction. The 63% mineralization in the case of EF treatment was due to the formation of short intermediates, such as carboxylic acids, which were difficult to oxidise with center dot OH. In the AO-H(2)O(2)-UVA process, about 36% of the TOC was removed after 6 h electrolysis, while 28% of the TOC was removed in the AO-H(2)O(2) process. SMX is only slightly mineralized by the AO process, with only 25% of the TOC removed. HPLC-MS analysis allowed for up to six aromatic reaction products to be identified during the SMX degradation in the PEF process, mainly formed from the hydroxylation of the aromatic ring or/and isoxazole ring, accompanied by the substitution of the amine group (on aromatic cycle) or methyl group (on isoxazole ring) by center dot OH. The carboxylic acids generated, including oxalic, maleic, oxamic, formic and acetic acids, were detected by ion-exclusion chromatography. The initial organic nitrogen was mainly converted into NH(4)(+) along with a very small proportion of NO(3)(-) ion. Considering all the oxidation intermediates and end products for SMX degradation in the PEF process, a general mineralization mechanism by center dot OH and UVA was proposed. (C) 2010 Elsevier BM. All rights reserved.