粤港澳大湾区某大城市水库水体全氟和多氟物质及其生态风险

IF 12.3 Q1 ENVIRONMENTAL SCIENCES Environmental Chemistry and Ecotoxicology Pub Date : 2025-01-01 Epub Date: 2025-01-26 DOI:10.1016/j.enceco.2025.01.009
Yiming Ge , Yi Huang , Linshen Xie , Chenglin Li , Xiujuan Qi , Pu Ye , Xixiang Guo , Chen Deng , Rong Hu , Bei Wang , Jinling Wang , Yihong Liu , Jiayi Xu , Tingting Zhu , Shaoyou Lu
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引用次数: 0

摘要

全氟和多氟物质(PFASs)是具有热稳定性和化学稳定性的合成化学品,广泛用于食品包装、消防泡沫、不粘涂料和润滑剂等消费品。它们对人类健康和水生生态系统的潜在威胁促使人们限制了它们的使用。然而,由于它们的环境持久性,它们仍然广泛存在于淡水系统中。鉴于水库是沿海城市居民重要的饮用水源,本研究采集了深圳市及其特别合作区35个水库的水样,量化了17种PFASs。分析了污染物浓度的季节和空间分布,评价了生态风险。结果显示,尽管全氟烷烃磺酸(PFSAs)很少被检测到,但全氟烷基磺酸在各种储层中广泛存在。枯水期ΣPFASs浓度(中位数:20.5 ng/L)显著高于丰水期(6.58 ng/L),可能与降雨后的稀释效应有关。五氟辛酸(中位数:2.76 ng/L)和全氟正丁酸(3.90 ng/L)分别在湿季和旱季占主导地位。在空间分布上,枯水期支流中ΣPFASs浓度明显高于水库中(中位数:58.1 ng/L vs. 20.5 ng/L),这可能是由于污染物湿沉降减少和支流水流流动性降低所致。此外,在旱季,短链PFASs的浓度显著高于长链PFASs(中位数:16.0 ng/L vs. 3.10 ng/L),这可能与短链化合物的广泛应用有关。总体而言,水库中PFASs对生态系统和人类的风险不显著。未来可能有必要制定有关氟化工厂的法规,以减少全氟磺酸的使用和排放。此外,后续的研究可以包括更大范围的样本,以更好地估计具有不同链长和官能团的PFASs对水生环境构成的潜在风险。
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Per- and polyfluorinated substances in reservoir water from a metropolitan city in the Guangdong-Hong Kong-Macao Greater Bay Area, China, and their ecological risks
Per- and polyfluorinated substances (PFASs) are synthetic chemicals with thermal and chemical stability, widely used in consumer products such as food packaging, fire-fighting foams, non-stick coatings, and lubricants. Their potential threats to human health and aquatic ecosystems have prompted restrictions on their usage. However, they are still widely found in freshwater systems due to their environmental persistence. Given that reservoirs are a vital source of drinking water for coastal city residents, this study collected water samples from 35 reservoirs in SZ City and its special cooperation zone to quantify 17 PFASs. Seasonal and spatial distributions of contaminant concentrations were analyzed and ecological risks were assessed. The results showed a widespread presence of PFASs in various reservoirs, although perfluoroalkane sulfonic acids (PFSAs) were infrequently detected. The concentration of ΣPFASs in the dry season (median: 20.5 ng/L) was significantly higher than that in the wet season (6.58 ng/L), likely attributable to a dilution effect after rainfall. Pentadecafluorooctanoic acid (median: 2.76 ng/L) and perfluoro-n-butanoic acid (3.90 ng/L) dominated in the wet and dry seasons, respectively. For spatial distribution, the ΣPFASs concentration in tributaries was markedly higher than that in reservoirs during the dry seasons (median: 58.1 ng/L vs. 20.5 ng/L), probably due to the diminished wet deposition of contaminants and the reduced mobility of tributary water flow. Furthermore, the concentration of short-chain PFASs was significantly greater than that of long-chain PFASs in the dry seasons (median: 16.0 ng/L vs. 3.10 ng/L), possibly related to the widespread application of short-chain compounds. Overall, the risk to the ecosystem and humans from PFASs in reservoirs is not significant. Future regulations on fluorochemical plants may be warranted to reduce the use and discharge of PFASs. Also, subsequent studies could include a wider range of samples to better estimate the potential risk posed by PFASs with varying chain lengths and functional groups to aquatic environment.
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