Electrochemical incineration of the antibiotic ciprofloxacin in sulfate medium and synthetic urine matrix

Autor: Sergi Garcia-Segura, Enric Brillas, V. S. Antonin, Mauro C. Santos
Rok vydání: 2015
Předmět:
Zdroj: Water Research. 83:31-41
ISSN: 0043-1354
DOI: 10.1016/j.watres.2015.05.066
Popis: The degradation of 100 mL of 0.245 mM of the antibiotic ciprofloxacin in 0.05 M Na 2 SO 4 at pH 3.0 has been studied by electrochemical oxidation with electrogenerated H 2 O 2 (EO-H 2 O 2 ), electro-Fenton (EF), UVA photoelectro-Fenton (PEF) and solar PEF (SPEF). Electrolyses were performed with a stirred tank reactor using either a boron-doped diamond (BDD) or Pt anode and an air-diffusion cathode. In EF, PEF and SPEF, ciprofloxacin was rapidly removed due to its oxidation with • OH formed from Fenton's reaction between added Fe 2+ and H 2 O 2 generated at the cathode. The larger electrochemical incineration of the antibiotic was achieved by SPEF with BDD with 95% mineralization thanks to the additional attack by hydroxyl radicals formed from water oxidation at the BDD anode surface and the photolysis of final Fe(III)-oxalate and Fe(III)-oxamate species from sunlight. Up to 10 primary intermediates and 11 hydroxylated derivatives were identified by LC-MS, allowing the proposal of a reaction sequence for ciprofloxacin mineralization. A different behavior was found when the same antibiotic concentration was oxidized in a synthetic urine matrix with high urea content and a mixture of PO 4 3 − , SO 4 2 − and Cl − ions. Since Fenton's reaction was inhibited in this medium, only EO and EO-H 2 O 2 processes were useful for mineralization, being the organics mainly degraded by HClO formed from Cl − oxidation. The EO process with a BDD/stainless steel cell was found to be the most powerful treatment for the urine solution, yielding 96% ciprofloxacin removal and 98% mineralization after 360 min of electrolysis at optimum values of pH 3.0 and current density of 66.6 mA cm −2 . The evolution of released inorganic ions was followed by ion chromatography.
Databáze: OpenAIRE