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电过氧协同作用工艺去除二级出水中的药物。

Removal of pharmaceuticals from secondary effluents by an electro-peroxone process.

机构信息

School of Environment, Beijing Key Laboratory for Emerging Organic Contaminants Control, State Key Joint Laboratory of Environmental Simulation and Pollution Control, Tsinghua University, Beijing 100084, China.

School of Environment, Beijing Key Laboratory for Emerging Organic Contaminants Control, State Key Joint Laboratory of Environmental Simulation and Pollution Control, Tsinghua University, Beijing 100084, China.

出版信息

Water Res. 2016 Jan 1;88:826-835. doi: 10.1016/j.watres.2015.11.024. Epub 2015 Nov 12.

Abstract

This study compared the removal of pharmaceuticals from secondary effluents of wastewater treatment plants (WWTPs) by conventional ozonation and the electro-peroxone (E-peroxone) process, which involves electrochemically generating H2O2 in-situ from O2 in sparged O2 and O3 gas mixture (i.e., ozone generator effluent) during ozonation. Several pharmaceuticals with kO3 ranging from <0.1 to 6.8 × 10(5) M(-1) s(-1) were spiked into four secondary effluents collected from different WWTPs, and then treated by ozonation and the E-peroxone process. Results show that both processes can rapidly remove ozone reactive pharmaceuticals (diclofenac and gemfibrozil), while the E-peroxone process can considerably accelerate the removal of ozone-refractory pharmaceuticals (e.g., ibuprofen and clofibric acid) via indirect oxidation with OH generated from the reaction of sparged O3 with electro-generated H2O2. Compared with ozonation, the E-peroxone process enhanced the removal kinetics of ozone-refractory pharmaceuticals in the four secondary effluents by ∼40-170%, and the enhancement was more pronounced in secondary effluents that had relatively lower effluent organic matter (EfOM). Due to its higher efficiency for removing ozone-refractory pharmaceuticals, the E-peroxone process reduced the reaction time and electrical energy consumption required to remove ≥90% of all spiked pharmaceuticals from the secondary effluents as compared to ozonation. These results indicate that the E-peroxone process may provide a simple and effective way to improve existing ozonation system for pharmaceutical removal from secondary effluents.

摘要

本研究比较了传统臭氧氧化法和电过氧(E-peroxone)工艺从污水处理厂(WWTP)二级出水去除药物的效果,后者涉及在臭氧氧化过程中通过电化学原位从注入的 O2 和 O3 气体混合物(即臭氧发生器流出物)中产生 H2O2。将几种 kO3 值范围为 <0.1 至 6.8×10(5) M(-1) s(-1) 的药物加入到从四个不同 WWTP 收集的四个二级出水中,然后用臭氧氧化法和 E-peroxone 工艺进行处理。结果表明,两种工艺都可以快速去除臭氧反应性药物(双氯芬酸和吉非贝齐),而 E-peroxone 工艺可以通过与注入的 O3 反应生成的 OH 间接氧化,显著加快臭氧难降解药物(如布洛芬和氯贝酸)的去除。与臭氧氧化相比,E-peroxone 工艺在四个二级出水中增强了臭氧难降解药物的去除动力学,提高了约 40-170%,在有机污染物(EfOM)相对较低的二级出水中,增强效果更为显著。由于 E-peroxone 工艺在去除二级出水中所有添加药物时所需的反应时间和电能消耗方面的效率更高,因此可用于改善现有的臭氧氧化系统以去除药物。

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