Electrochemical degradation of aqueous solutions containing antibiotic amoxicillin (AMX) has been extensively studied in an undivided electrolytic cell using a sub-stoichiometric titanium oxide (TiO) anode, elaborated by plasma deposition. Oxidative degradation of AMX by hydroxyl radicals was assessed as a function of applied current and was found to follow pseudo-first order kinetics. The use of carbon-felt cathode enhanced oxidation capacity of the process due to the generation of HO. Comparative studies at low current intensity using dimensional stable anode (DSA) and Pt anodes led to the lower mineralization efficiencies compared to TiO anode: 36 and 41% TOC removal for DSA and Pt respectively compared to 69% for TiO anode. Besides, the use of boron doped diamond (BDD) anode under similar operating conditions allowed reaching higher mineralization (94%) efficiency. Although TiO anode provides a lesser mineralization rate compared to BDD, it exhibits better performance compared to the classical anodes Pt and DSA and can constitutes an alternative to BDD anode for a cost effective electro-oxidation process. Moreover several aromatic and aliphatic oxidation reaction intermediates and inorganic end-products were identified and a plausible mineralization pathway of AMX involving these intermediates was proposed.
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http://dx.doi.org/10.1016/j.watres.2016.09.056 | DOI Listing |
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