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青霉素生产废水处理厂及受纳河流中青霉素G及其降解产物的测定

Determination of penicillin G and its degradation products in a penicillin production wastewater treatment plant and the receiving river.

作者信息

Li Dong, Yang Min, Hu Jianying, Zhang Yu, Chang Hong, Jin Fen

机构信息

State Key Laboratory of Environmental Aquatic Chemistry, Research Center for Eco-Environmental Sciences, Chinese Academy of Sciences, Beijing 100085, China.

出版信息

Water Res. 2008 Jan;42(1-2):307-17. doi: 10.1016/j.watres.2007.07.016. Epub 2007 Jul 20.

Abstract

To investigate the fate of penicillin G (PEN G) in the wastewater from a PEN G production facility and the receiving river, an analytical method was developed for the simultaneous detection of PEN G and five degradation products using liquid chromatography-electrospray ionization mass spectrometry (LC-ESI/MS). PEN G had already undergone transformation before entering into the wastewater treatment plant (WWTP), with concentrations of 153+/-4 microg/L in raw wastewater. Most of the PEN G could be eliminated following successive treatments of anaerobic, hydrolysis, and two aerobic units under a hydraulic residence time (HRT) of 30 h, and the final concentrations were 1.68+/-0.48 microg/L in treated water. In the receiving river, the concentration of PEN G decreased from 0.31+/-0.04 microg/L at the discharging point to under the detection limit (0.03 microg/L) at the last sampling site (about 30 km from the discharging point). The main PEN G degradation products in surface water were found to be penilloic acid, penicilloic acid and isopenillic acid, which occupied 65.8%, 20.4% and 12.9%, respectively, of the total concentration at the last site. This is the first study on the behaviors of PEN G and its main degradation products in wastewater treatment processes and the aquatic environment.

摘要

为了研究青霉素G(PEN G)在青霉素生产设施废水及受纳河流中的去向,开发了一种采用液相色谱-电喷雾电离质谱(LC-ESI/MS)同时检测青霉素G及其五种降解产物的分析方法。青霉素G在进入污水处理厂(WWTP)之前就已经发生了转化,原废水中的浓度为153±4μg/L。在水力停留时间(HRT)为30小时的情况下,经过厌氧、水解和两个好氧单元的连续处理后,大部分青霉素G可以被去除,处理后水中的最终浓度为1.68±0.48μg/L。在受纳河流中,青霉素G的浓度从排放点的0.31±0.04μg/L降至最后一个采样点(距离排放点约30公里)的检测限(0.03μg/L)以下。地表水中青霉素G的主要降解产物为青霉噻唑酸、青霉酸和异青霉酸,在最后一个采样点分别占总浓度的65.8%、20.4%和12.9%。这是关于青霉素G及其主要降解产物在废水处理过程和水环境中行为的首次研究。

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