Ti/Ta2O5/Pt-RuO2-IrO22电极上阿莫西林的电化学降解

A. F. T. Auguste, L. Ouattara
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引用次数: 4

摘要

本文研究了阿莫西林的降解,阿莫西林是人类和兽药中常用的抗生素之一。采用Pt-RuO2-IrO2 (PRI)电极作为阳极,对电流密度(20 ~ 100 mA/cm2)、支撑电解质和氯化物等参数进行监测。结果表明,阿莫西林氧化反应受扩散控制,其降解速率随外加电流的增大而增大。在没有氯化物的情况下,PRI电极对阿莫西林的降解率很低,不到COD消减率的10%。但是,在氯离子存在下,PRI电极上阿莫西林的降解导致其矿化。在电解过程中,氯化物在pH ?下被氧化成HClO形式的氯。在pH > 8的条件下,导致阿莫西林的显著降解。无氯和有氯时,阿莫西林的去除率从0.83%提高到73.8%。,电解10h后分别为。此外,阿莫西林在HClO4中的降解动力学比在KClO4中快10倍,并遵循准一级反应。
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Electrochemical Degradation of Amoxicillin on a Ti/Ta2O5/Pt-RuO2-IrO22 Electrode
This work deals with the degradation of Amoxcillin which is one of the antibiotics commonly used in human and veterinary medicine. For such an investigation, Pt-RuO2-IrO2 (PRI) electrode was used as anode and various parameters such as current density (20 - 100 mA/cm2), supporting electrolyte and chloride were monitored. The results showed that the amoxicillin oxidation reaction is diffusion controlled and its degradation rate increases as the applied current increases. The degradation of amoxicillin on the PRI electrode, in the absence of chloride, is very low with less than 10% of the COD abatement rate. But, in the presence of chloride, the degradation of the Amoxicillin on PRI electrode leads to its mineralization. During electrolysis, chloride was oxidized into chlorine under the form HClO at pH ? at pH > 8 that contribute to a significant degradation of the Amoxicillin. The amoxicillin removal rate goes from 0.83% to 73.8% in the absence and in the presence of Cl?, respectively after 10 h of electrolysis. In addition, the degradation kinetic of amoxicillin in HClO4 is 10 times faster than in KClO4 and follows pseudo first-order reaction.
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