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Electrochemical Oxidation of Pharmaceuticals on a Pt-SnO2/Ti Electrode

机译:Pt-SnO2/Ti电极上药物的电化学氧化

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The application of an advanced oxidation process, electrochemical oxidation, was evaluated for the degradation of the non-steroidal anti-inflammatory substance, diclofenac (DCF), by using an electrode (anode) of Pt-SnO2 on a titanium substrate (Pt-SnO2/Ti). An increased decomposition rate of DCF was recorded. Different experimental parameters such as current intensity, initial concentration of substrate, irradiation, and pH were evaluated. The effects of bicarbonate and chloride ions and humic acid (HA) were also assessed. It was found that the electrochemical degradation follows pseudo-first-order kinetic with respect to the initial substrate concentration. The kinetics rate constant was shown to increase with increasing chloride concentration and current intensity, while it decreased with increasing initial DCF concentration. Additionally, the results showed that the concentration of bicarbonate ions slightly diminishes the process yield, while ultraviolet A (UVA) irradiation does not accelerate DCF decomposition. In contrast, lower pH values contributed to faster degradation of the target substance. The effect of the aqueous matrix was also evaluated. A higher rate of DCF decomposition within a shorter time interval was recorded when secondary effluent (WW) was used. On the contrary, HA was found to slow down the process. Finally, experiments were carried out to investigate the degradation of another pharmaceutical, sulfamethoxazole (SMX). It was found that SMX was degraded at 73.1 in 30 min, while for the same time; the abatement of DCF was 44.5. This study demonstrates the efficiency of electrochemical oxidation for the abatement of pharmaceuticals with an anode of platinum-tin dioxide on titanium substrate in water matrices.
机译:通过使用钛基板 (Pt-SnO2/Ti) 上的 Pt-SnO2 电极(阳极),评估了先进氧化工艺电化学氧化的应用,以降解非甾体抗炎物质双氯芬酸 (DCF)。记录到DCF的分解速率增加。评估了电流强度、底物初始浓度、辐照度和pH值等不同实验参数。还评估了碳酸氢盐和氯离子以及腐植酸(HA)的影响。结果发现,电化学降解相对于初始衬底浓度遵循准一级动力学。动力学速率常数随氯化物浓度和电流强度的增加而增加,而动力学速率常数随初始DCF浓度的增加而降低。此外,结果表明,碳酸氢根离子的浓度会略微降低工艺产率,而紫外线A(UVA)照射不会加速DCF分解。相反,较低的pH值有助于更快地降解目标物质。还评估了水性基质的影响。当使用二次流出物 (WW) 时,在较短的时间间隔内记录了更高的 DCF 分解速率。相反,医管局被发现会减慢这一过程。最后,进行了实验,研究了另一种药物磺胺甲噁唑(SMX)的降解情况。结果发现,SMX在30 min内降解率为73.1%,而在同一时间;DCF的减少率为44.5%。本研究证明了电化学氧化对水基质中钛基底上二氧化铂锡阳极的药物减排的效率。

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