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Removal and transformation of pharmaceuticals in wastewater treatment plants and constructed wetlands

机译:废水处理厂和人工湿地中药物的去除和转化

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摘要

Since trace organic compounds such as pharmaceuticals in surface water have been a relevant threat to drinking water supplies, in this study removal of pharmaceuticals and transformation of pharmaceuticals into metabolites were investigated in the main source of micropollutants such as WWTPs and engineered constructed wetlands. Pharmaceuticals were effectively removed by different WWTP processes and wetlands. Pharmaceutical metabolites with relatively low log D value were resulted in the low removal efficiencies compared to parent compounds with relatively high log D value, indicating the stability of metabolites. And the constructed wetlands fed with wastewater effluent were encouraged to prevent direct release of micropollutants into surface waters. Among various pharmaceuticals, different transformation pattern of ibuprofen was observed with significant formation of 1-hydroxy-ibuprofen during biological treatment in WWTP, indicating preferential biotransformation of ibuprofen. Lastly, transformation of pharmaceuticals depending on their structural position was investigated in terms of electron density, and, the electron rich C1 = C2 bond of carbamazepine was revealed as an initial transformation position.
机译:由于地表水中的痕量有机化合物(例如药物)已成为饮用水供应的相关威胁,因此在这项研究中,我们在诸如WWTP和工程人工湿地等微污染物的主要来源中研究了药物的去除以及药物向代谢物的转化。通过不同的污水处理厂工艺和湿地有效地去除了药品。与具有相对较高log D值的母体化合物相比,具有相对较低log D值的药物代谢物的去除效率较低,这表明代谢物的稳定性。并鼓励人工喂养的废水进入湿地,以防止微量污染物直接释放到地表水中。在各种药物中,观察到不同的布洛芬转化模式,在污水处理厂的生物处理过程中会形成1-羟基-布洛芬,这表明布洛芬具有优先的生物转化能力。最后,根据电子密度研究了取决于其结构位置的药物转化,并将卡马西平的富电子C1 = C2键显示为初始转化位置。

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