Department of Environmental Science and Analytical Chemistry (ACES), Stockholm University , 10691 Stockholm, Sweden.
Environ Sci Technol. 2016 Jun 7;50(11):5614-21. doi: 10.1021/acs.est.5b06327. Epub 2016 May 19.
A considerable knowledge gap exists with respect to the fate and environmental relevance of transformation products (TPs) of polar organic micropollutants in surface water. To narrow this gap we investigated the fate of 20 parent compounds (PCs) and 11 characteristic TPs in four wastewater-impacted rivers. Samples were obtained from time-integrated active sampling as well as passive sampling using polar organic chemical integrative samplers (POCIS). Seventeen out of the 20 PCs were detected in at least one of the rivers. All the PCs except acesulfame, carbamazepine, and fluconazole were attenuated along the studied river stretches, with the largest decrease found in the smallest river which had an intense surface water-pore water exchange. Seven TPs were detected, all of which were already present directly downstream of the WWTP outfall, suggesting that the WWTPs were a major source of TPs to the recipients. For anionic compounds, attenuation was the highest in the two rivers with the lowest discharge, while the pattern was not as clear for neutral or cationic compounds. For most compounds the results obtained from active sampling were not significantly different from those using POCIS, demonstrating that the cost and labor efficient POCIS is suitable to determine the attenuation of organic micropollutants in rivers.
对于极性有机微污染物在地表水环境中的归趋和环境相关性,存在着相当大的知识空白。为了缩小这一差距,我们研究了 20 种母体化合物(PCs)和 11 种特征转化产物(TPs)在四条受废水影响的河流中的归趋。通过时间积分主动采样和使用极性有机化学整合采样器(POCIS)进行的被动采样,采集了样品。在所研究的河流中,至少有一条河流中检测到了 17 种 PC。除了乙酰磺胺酸、卡马西平和氟康唑外,所有的 PC 都沿着研究的河段被衰减,在最小的河流中发现的衰减最大,因为这条河流有强烈的地表水-孔隙水交换。检测到了 7 种 TPs,它们都直接在污水处理厂出水口的下游存在,这表明污水处理厂是这些 TPs 的主要来源。对于阴离子化合物,在两个流量最低的河流中衰减率最高,而对于中性或阳离子化合物,情况则不那么明显。对于大多数化合物,主动采样的结果与 POCIS 的结果没有显著差异,这表明成本和劳动效率高的 POCIS 适合于确定河流中有机微污染物的衰减。