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Diclofenac removal by pyrite-Fenton process: Performance in batch and fixed-bed continuous flow systems

机译:黄铁矿-Fenton工艺去除双氯芬酸:间歇和固定床连续流系统的性能

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This study provides experimental results from batch and column studies to investigate diclofenac degradation by pyrite-Fenton process under variable chemical conditions (e.g., pyrite loading). Batch experiments show that diclofenac removal increased with increasing hydrogen peroxide and pyrite concentration. On the other hand, the addition of organic chelating agents such as citrate had an adverse effect on diclofenac removal by pyrite-Fenton process in batch systems due to scavenging effect of these agents for hydroxyl radicals. Batch results showed a direct correlation between the rate of diclofenac degradation and the rate of iron dissolution from pyrite, suggesting that diclofenac removal by pyrite-Fenton process was mainly controlled by solution phase hydroxyl radical attack on aromatic structure. Column experiments show that the effluent diclofenac concentration initially reached a peak value, and then sharply decreased to zero at higher pore volumes. The initial diclofenac breakthrough coincided well with the highest Fe(II) concentration observed in the breakthrough curve, implying that the generation of excess Fe(II) had a detrimental effect on removal efficiency due to scavenging effect of excess Fe(II) for hydroxyl radicals. The column system continued to function with 100% diclofenac removal efficiency when the effluent Fe(II) concentration decreased to a level at which the scavenging effect was minimized. (C) 2019 Elsevier B.V. All rights reserved.
机译:这项研究提供了批次研究和柱研究的实验结果,以研究在可变化学条件(例如黄铁矿负载)下黄铁矿-Fenton工艺降解双氯芬酸的过程。批处理实验表明,双氯芬酸的去除随着过氧化氢和黄铁矿浓度的增加而增加。另一方面,由于这些螯合剂对羟基自由基的清除作用,添加有机螯合剂例如柠檬酸盐对黄铁矿-芬顿法在批料系统中的双氯芬酸去除有不利影响。批处理结果表明双氯芬酸的降解速率与铁从黄铁矿中溶解的速率之间存在直接相关性,这表明黄铁矿-芬顿法去除双氯芬酸主要受溶液相羟基自由基对芳族结构的攻击所控制。色谱柱实验表明,出水双氯芬酸浓度最初达到峰值,然后在较高的孔体积下急剧降至零。双氯芬酸的初始突破与在突破曲线中观察到的最高Fe(II)浓度很好地吻合,这表明由于过量Fe(II)对羟基自由基的清除作用,过量Fe(II)的产生对去除效率有不利影响。 。当流出液中的Fe(II)浓度降至清除效果最小的水平时,色谱柱系统继续以100%的双氯芬酸去除效率运行。 (C)2019 Elsevier B.V.保留所有权利。

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