MOE Key Laboratory of Pollution Processes and Environmental Criteria, College of Environmental Science and Engineering , Nankai University , Tianjin 300071 , China.
Wadsworth Center, New York State Department of Health, and Department of Environmental Health Sciences, School of Public Health , State University of New York at Albany , Albany , New York 12201 , United States.
Environ Sci Technol. 2018 Aug 7;52(15):8263-8271. doi: 10.1021/acs.est.8b00544. Epub 2018 Jul 11.
Industrial facilities can be point sources of per- and polyfluoroalkyl substances (PFASs) emission to the surrounding environment. In this study, 25 neutral and ionizable PFASs were analyzed in 94 multimedia samples including air, rain, outdoor settled dust, soil, plant leaves, river water, surface sediment, and shallow groundwater from two fluorochemical manufacturing parks (FMPs) in Fuxin, China, to elucidate the multimedia distribution and transfer pattern of PFASs from a point source. The concentrations of individual PFASs in air, outdoor settled dust, and surface river water decreased exponentially as the distance increases from the FMPs, whereas the concentrations of short-chain (C2-C4) perfluoroalkyl carboxylic acids (PFCAs) remained high (3000 ng/L) in the surface water 38 km away. At FMPs, air concentrations of fluorotelomer alcohols and iodides were found dominant with levels of up to 7900 pg/m and 920 pg/m, respectively. Trifluoroacetic acid was directly released from FMPs and occurred in all the environmental matrices at levels 1-2 orders of magnitude higher than other PFCAs. Higher air-water concentration ratios of short-chain PFCAs (C2-C4) suggested their transfer tendency from air to water. Both short-chain (C2) and long-chain (>C6) PFCAs have greater sediment-water distribution coefficients and deposit dust-air coefficients, which have great influences on the long-range transport potential of different analogues.
工业设施可能是向周围环境排放全氟和多氟烷基物质 (PFASs) 的点源。在这项研究中,分析了来自中国阜新的两个氟化学制造园区 (FMPs) 的 94 个多介质样本中的 25 种中性和可离子化的 PFASs,包括空气、雨水、室外沉降灰尘、土壤、植物叶片、河水、表层沉积物和浅层地下水,以阐明从点源 PFASs 的多介质分布和转移模式。随着与 FMPs 的距离增加,空气中、室外沉降灰尘中和地表水的个别 PFASs 浓度呈指数下降,而短链 (C2-C4) 全氟烷基羧酸 (PFCAs) 的浓度在 38 公里外的地表水仍保持高位 (3000ng/L)。在 FMPs 中,发现氟调聚物醇和碘化物的空气浓度占主导地位,分别达到 7900pg/m 和 920pg/m。三氟乙酸直接从 FMPs 释放出来,并在所有环境介质中出现,浓度比其他 PFCAs 高 1-2 个数量级。短链 (C2-C4) PFCAs 的空气-水浓度比较高,表明它们从空气向水中转移的趋势。短链 (C2) 和长链 (>C6) PFCAs 都具有更大的沉积物-水分配系数和沉积灰尘-空气系数,这对不同类似物的远距离迁移潜力有很大影响。