Electrochemical incineration of the antimicrobial sulfamethazine at a boron-doped diamond anode
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文摘
The electrochemical incineration of the antimicrobial sulfamethazine in acidic medium by anodic oxidation (AO) has been studied using an undivided or divided cell with a boron-doped diamond (BDD) anode and a stainless steel cathode. The oxidation power of AO with BDD was greater in the divided than in the undivided cell, as a result of the higher efficiency of reactive hydroxyl radicals generated at the BDD anode from water oxidation. A similar degradation rate was found over the pH range 2.0-6.0. The treatment of a 193 mg dm?3 drug solution in 0.50 mol dm?3 Na2SO4 at controlled pH 3.0 in the anodic compartment of the divided cell yielded 98 % mineralization for current densities ¡Ý 66.6 mA cm?2. Analogous almost total mineralization was attained using the undivided cell with 0.05 mol dm?3 Na2SO4 at current densities ¡Ý 100 mA cm?2, but with lower degradation rate and efficiency. Decreasing current density and increasing drug content enhanced the mineralization current efficiency. Reversed-phase HPLC allowed determining a pseudo-first-order kinetics for sulfamethazine decay, which was faster in the divided cell. 1,2-Benzenediol, 1,4-benzenediol, p-benzoquinone and 4,6-dimethyl-2-pyrimidinamine were identified as aromatic intermediates in the divided cell by gas chromatography-mass spectrometry. Generated carboxylic acids like maleic, fumaric, acetic, formic, oxalic and oxamic were quantified by ion-exclusion HPLC. Ionic chromatography revealed the conversion of the initial N of sulfamethazine into NH4+ ion, along with NO3? ion in much smaller proportion. From all detected intermediates, a reaction pathway for sulfamethazine mineralization in acidic medium by AO with BDD is proposed.

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