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               <dc:title>Fast and complete removal of the 5-fluorouracil drug from water by electro-Fenton oxidation</dc:title>
               <dc:creator>Ganzenko, Oleksandra</dc:creator>
               <dc:creator>Oturan, Nihal</dc:creator>
               <dc:creator>Sirés Sadornil, Ignacio</dc:creator>
               <dc:creator>Huguenot, David</dc:creator>
               <dc:creator>Hullebusch, Eric D. van</dc:creator>
               <dc:creator>Esposito, Giovanni</dc:creator>
               <dc:creator>Oturan, Mehmet A.</dc:creator>
               <dc:subject>Medicaments antineoplàstics</dc:subject>
               <dc:subject>Contaminació de l'aigua</dc:subject>
               <dc:subject>Descontaminació</dc:subject>
               <dc:subject>Antineoplastic agents</dc:subject>
               <dc:subject>Water pollution</dc:subject>
               <dc:subject>Decontamination</dc:subject>
               <dc:description>Cytostatic drugs are a troublesome class of emerging pollutants in water owing to their potential effects on DNA. Here we studied the removal of 5-fluorouracil from water using the electro-Fenton process. Galvanostatic electrolyses were performed with an undivided laboratory-scale cell equipped with a boron-doped diamond anode and a carbon felt cathode. Results show that the fastest degradation and almost complete mineralization was obtained at a Fe2+ catalyst concentration of 0.2 mM. The absolute rate constant for oxidation of 5-fluorouracil by hydroxyl radicals was 1.52 × 109 M−1 s−1. Oxalic and acetic acids were initially formed as main short-chain aliphatic by-products, then were completely degraded. After 6 h the final solution mainly contained inorganic ions (NH4 +, NO3 − and F−) and less than 10% of residual organic carbon. Hence, electro-Fenton constitutes an interesting alternative to degrade biorefractory drugs.</dc:description>
               <dc:date>2019-05-22T09:23:17Z</dc:date>
               <dc:date>2019-05-22T09:23:17Z</dc:date>
               <dc:date>2018-03</dc:date>
               <dc:date>2019-05-22T09:23:17Z</dc:date>
               <dc:type>info:eu-repo/semantics/article</dc:type>
               <dc:type>info:eu-repo/semantics/acceptedVersion</dc:type>
               <dc:relation>Versió postprint del document publicat a: https://doi.org/10.1007/s10311-017-0659-6</dc:relation>
               <dc:relation>Environmental Chemistry Letters, 2018, vol. 16, num. 1, p. 281-286</dc:relation>
               <dc:relation>https://doi.org/10.1007/s10311-017-0659-6</dc:relation>
               <dc:rights>(c) Springer Verlag, 2018</dc:rights>
               <dc:rights>info:eu-repo/semantics/openAccess</dc:rights>
               <dc:publisher>Springer Verlag</dc:publisher>
               <dc:source>Articles publicats en revistes (Ciència dels Materials i Química Física)</dc:source>
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