Liu Zhaoyang, Lu Yonglong, Wang Tieyu, Wang Pei, Li Qifeng, Johnson Andrew C, Sarvajayakesavalu Suriyanarayanan, Sweetman Andrew J
State Key Laboratory of Urban and Regional Ecology, Research Center for Eco-Environmental Sciences, Chinese Academy of Sciences, Beijing 100085, China; University of Chinese Academy of Sciences, Beijing 100049, China.
State Key Laboratory of Urban and Regional Ecology, Research Center for Eco-Environmental Sciences, Chinese Academy of Sciences, Beijing 100085, China.
Environ Int. 2016 May;91:69-77. doi: 10.1016/j.envint.2016.02.020. Epub 2016 Feb 22.
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 10km 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 1.86mg/L in the nearby rivers flowing to the Bohai sea together with up to 273μg/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 4km, and at least 3km 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.
全氟烷基酸(PFAAs)可在含PFAA产品的制造和应用过程中释放到水体中。在本研究中,对一个大型氟化工产业园区(FIP)半径10公里范围内地表水和地下水中PFAAs的污染模式、衰减动态、来源、途径和风险分区进行了研究。在检测到的12种PFAAs中,全氟辛酸(PFOA)占主导地位,其次是短链全氟烷基羧酸(PFCAs)。含PFAA的废物从FIP排放,流入渤海的附近河流中其含量达到1.86mg/L,集水区当地地下水中含量高达273μg/L。这些含量对该地点的PFOA和其他短链PFCAs构成了人类健康风险。地表水中∑PFAAs的浓度与当地地下水密切相关。PFAAs的主要污染途径包括:(i)排放到地表水,然后通过渗漏进入地下水;(ii)从FIP进行大气沉降,随后渗入地下水。随着与源头距离的增加,地下水中PFAAs的含量最初急剧下降,随后缓慢下降。FIP场地对地下水中PFAAs的污染信号存在于半径4公里范围内,距离受污染的东朱龙河至少3公里。PFAA衰减过程中的主要控制因素可能是稀释以及向含水层固体的扩散和吸附。在地表水渗漏和在地下水中进一步扩散过程中,PFOA(C8)的相对丰度下降,而短链PFCAs(C4 - C6)的相对丰度增加。