| Literature DB >> 29554628 |
A S Ochoa-Chavez1, A Pieczyńska2, A Fiszka Borzyszkowska2, P J Espinoza-Montero1, E M Siedlecka3.
Abstract
In this study, the electrochemical degradation process of 5-fluorouracil (5-FU) in aqueous media was performed using a continuous flow reactor in an undivided cell (system I), and in a divided cell with a cationic membrane (Nafion® 424) (system II). In system I, 75% of 5-FU degradation was achieved (50 mg L-1) with a applied current density japp = 150 A m-2, volumetric flow rate qv = 13 L h-1, after 6 h of electrolysis (kapp = 0.004 min-1). The removal efficiency of 5-FU was higher (95%) when the concentration was 5 mg L-1 under the same conditions. Nitrates (22% of initial amount of N), fluorides (27%) and ammonium (10%) were quantified after 6 h of electrolysis. System II, 77% of 5-FU degradation was achieved (50 mg L-1) after 6 h of electrolysis (kapp = 0.004 min-1). The degradation rate of 5-FU was complete when the concentration was 5 mg L-1 under the same conditions. Nitrates (29% of initial amount of N), fluorides (25%) and ammonium (5%) were quantified after 6 h of electrolysis. In addition, the main organic byproducts identified by mass spectroscopy were aliphatic compound with carbonyl and carboxyl functionalities. Due to, the mineralization of 5-FU with acceptable efficiency of 88% found in system II (japp of 200 A m-2), this system seems to be more promising in the cytostatic drug removal. Moreover the efficiency of 5-FU removal in diluted solutions is better in system II than in system I.Entities:
Keywords: 5-Fluorouracil; BDD anode; Cytostatic drug; Electrochemical oxidation; Flow reactor
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Year: 2018 PMID: 29554628 DOI: 10.1016/j.chemosphere.2018.03.050
Source DB: PubMed Journal: Chemosphere ISSN: 0045-6535 Impact factor: 7.086