Eawag, Swiss Federal Institute of Aquatic Science and Technology, Dübendorf 8600, Switzerland.
Institute of Biogeochemistry and Pollutant Dynamics, ETH Zürich, Zürich 8092, Switzerland.
Environ Sci Technol. 2020 Apr 7;54(7):4110-4120. doi: 10.1021/acs.est.9b07085. Epub 2020 Mar 25.
This study presents a nontarget approach to detect discharges from pharmaceutical production in municipal wastewater treatment plant (WWTP) effluents and to estimate their relevance on the total emissions. Daily composite samples were collected for 3 months at two WWTPs in Switzerland, measured using liquid chromatography high-resolution mass spectrometry, and time series were generated for all features detected. The extent of intensity variation in the time series was used to differentiate relatively constant domestic inputs from highly fluctuating industrial emissions. We show that an intensity variation threshold of 10 correctly classifies compounds of known origin and reveals clear differences between the two WWTPs. At the WWTP receiving wastewater from a pharmaceutical manufacturing site, (i) 10 times as many potential industrial emissions were detected as compared to the WWTP receiving purely domestic wastewater; (ii) for 11 pharmaceuticals peak concentrations, >10 μg/L and up to 214 μg/L were quantified, which are clearly above typical municipal wastewater concentrations; and (iii) a pharmaceutical not authorized in Switzerland was identified. Signatures of potential industrial emissions were even traceable at the downstream Rhine monitoring station at a >4000-fold dilution. Several of them occurred repeatedly, suggesting that they were linked to regular production, not to accidents. Our results demonstrate that small wastewater volumes from a single industry not only left a clear signature in the effluents of the respective WWTP but also influenced the water quality of one of Europe's most important river systems. Overall, these findings indicate that pharmaceutical production is a relevant emission source even in highly developed countries with a strong focus on water quality, such as Switzerland.
本研究提出了一种非靶向方法,用于检测医药生产厂排放的物质在城市污水处理厂(WWTP)废水中的排放情况,并估计其对总排放量的相关性。在瑞士的两个 WWTP 中,每天采集三个月的混合样本,使用液相色谱高分辨率质谱进行测量,并为所有检测到的特征生成时间序列。时间序列中强度变化的程度用于区分相对恒定的生活污水输入和高度波动的工业排放。我们表明,强度变化阈值为 10 可以正确分类已知来源的化合物,并揭示了两个 WWTP 之间的明显差异。在接收制药厂废水的 WWTP 中,(i) 检测到的潜在工业排放是接收纯生活污水 WWTP 的 10 倍;(ii) 定量了 11 种药物的峰值浓度,>10μg/L 至 214μg/L,明显高于典型的城市污水浓度;(iii) 发现了一种未在瑞士授权的药物。即使在下游莱茵河监测站以 >4000 倍的稀释度,也能追踪到潜在工业排放的特征。其中一些特征反复出现,表明它们与常规生产有关,而不是与事故有关。我们的研究结果表明,即使在像瑞士这样对水质高度重视的高度发达的国家,来自单个行业的少量废水不仅在各自 WWTP 的废水中留下了明显的特征,而且还影响了欧洲最重要的河流系统之一的水质。总的来说,这些发现表明,即使在像瑞士这样高度发达、高度重视水质的国家,医药生产也是一个重要的排放源。