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Risk assessment and source identification of perfluoroalkyl acids in surface and ground water:spatial distribution around a mega-fluorochemical industrial park, China

机译:地表水和地下水中全氟烷基酸的风险评估和来源识别:中国超大型氟化工业园区周围的空间分布

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摘要

Perfluoroalkyl acids (PFAAs) can be released to water bodies during manufacturing and application of PFAA-containing products. In this study, the contamination pattern, attenuation dynamics, sources, pathways, and risk zoning of PFAAs in surface and ground water was examined within a 10 km radius from a mega-fluorochemical industrial park (FIP). Among 12 detected PFAAs, perfluorooctanoic acid (PFOA) dominated, followed by shorter-chained perfluoroalkyl carboxylic acids (PFCAs). PFAA-containing waste was discharged from the FIP, with levels reaching 1.86 mg/L in the nearby rivers flowing to the Bohai sea together with up to 273 μg/L in the local groundwater in the catchment. These levels constitute a human health risks for PFOA and other shorter-chained PFCAs within this location. The concentrations of ∑ PFAAs in surface water strongly correlated with the local groundwater. The dominant pollution pathways of PFAAs included (i) discharge into surface water then to groundwater through seepage, and (ii) atmospheric deposition from the FIP, followed by infiltration to groundwater. As the distance increased from the source, PFAAs levels in groundwater showed a sharp initial decrease followed by a gentle decline. The contamination signal from the FIP site on PFAAs in groundwater existed within a radius of 4 km, and at least 3 km from the polluted Dongzhulong River. The major controlling factor in PFAA attenuation processes was likely to be dilution together with dispersion and adsorption to aquifer solids. The relative abundance of PFOA (C8) declined while those of shorter-chained PFCAs (C4–C6) increased during surface water seepage and further dispersion in groundwater.
机译:在制造和使用含PFAA的产品期间,全氟烷基酸(PFAAs)可能释放到水体中。在这项研究中,在距巨型氟化物工业园区(FIP)10公里的半径范围内,研究了地表水和地下水中PFAAs的污染模式,衰减动力学,来源,途径和风险区划。在检测到的12种PFAA中,全氟辛酸(PFOA)占主导,其次是短链全氟烷基羧酸(PFCA)。从FIP排放出含PFAA的废物,在流入渤海的附近河流中,该污染物的浓度达到1.86 mg / L,而在该流域的当地地下水中的含量高达273μg/ L。这些水平对该地点内的PFOA和其他短链PFCA构成了人类健康风险。地表水中的∑ PFAAs浓度与当地地下水高度相关。 PFAAs的主要污染途径包括:(i)渗入地表水,然后通过渗漏排入地下水;(ii)FIP的大气沉积,然后渗入地下水。随着距离源头距离的增加,地下水中PFAAs的含量开始出现急剧下降,然后逐渐下降。来自PFAAs的FIP站点的地下水中的污染信号存在于半径4 km之内,并且距受污染的东祝龙河至少3 km。 PFAA衰减过程中的主要控制因素可能是稀释,分散和对含水层固体的吸附。在地表水渗透和地下水进一步扩散过程中,PFOA(C8)的相对丰度下降,而短链PFCA(C4–C6)的相对丰度增加。

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