色谱 ›› 2025, Vol. 43 ›› Issue (8): 940-949.DOI: 10.3724/SP.J.1123.2024.09004

• 研究论文 • 上一篇    下一篇

我国东部饮用水源水中传统及新型全氟和多氟烷基物质的赋存特征及风险评估

刘姜龙1,2, 张冰1, 古文1, 范德玲1, 王蕾1,*(), 付翯云2, 耿柠波3, 孙帅1,*()   

  1. 1.生态环境部南京环境科学研究所,江苏 南京 210042
    2.南京大学环境学院,江苏 南京 210023
    3.中国科学院大连化学物理研究所,辽宁 大连 116023
  • 收稿日期:2024-09-12 出版日期:2025-08-08 发布日期:2025-07-28
  • 通讯作者: E-mail:sunshuai@nies.org(孙帅);E-mail:wanglei@nies.org(王蕾).
  • 基金资助:
    中央级公益性科研院所基本科研业务专项(ZX2023QT003);中央级公益性科研院所基本科研业务专项(GYZX240403);国家自然科学基金(22306130)

Occurrence, characteristics, and risk assessment of legacy and novel per- and polyfluoroalkyl substances in drinking water sources of Eastern China

LIU Jianglong1,2, ZHANG Bing1, GU Wen1, FAN Deling1, WANG Lei1,*(), FU Heyun2, GENG Ningbo3, SUN Shuai1,*()   

  1. 1. Nanjing Institute of Environmental Sciences,Ministry of Ecology and Environment of the People’s Republic of China,Nanjing 210042,China
    2. School of Environment,Nanjing University,Nanjing 210023,China
    3. Dalian Institute of Chemical Physics,Chinese Academy of Sciences,Dalian 116023,China
  • Received:2024-09-12 Online:2025-08-08 Published:2025-07-28
  • Supported by:
    Central Scientific Research Projects for Public Welfare Research Institutes(ZX2023QT003);Central Scientific Research Projects for Public Welfare Research Institutes(GYZX240403);National Natural Science Foundation of China(22306130)

摘要:

为探明我国东部地区饮用水源水中传统及新型全氟和多氟烷基物质(PFAS)的赋存情况及潜在风险,采用弱阴离子交换固相萃取-超高效液相色谱-三重四极杆质谱法(UPLC-MS/MS)分析了东部地区13处饮用水源地水样中50种传统及新型PFAS的污染水平和分布特征,并开展了生态及健康风险评估。结果表明,我国东部地区饮用水源水中共检出26种PFAS,总含量为80.0~282 ng/L,中位值为153 ng/L。东部地区饮用水源水中PFAS的检出水平相对较高,但全氟辛酸(PFOA)和全氟辛基磺酸(PFOS)的水平远低于我国生活饮用水卫生标准限值。饮用水源水中检出的PFAS以短链的全氟丁酸(PFBA)和全氟丁烷磺酸(PFBS)为主,二者分别占总PFAS含量的27.6%和20.8%;而长链PFAS(碳链长度>9)的占比低于2%。尽管检出水平较低,但在东部地区饮用水源水中已发现多种新型PFAS。相关性分析结果表明,饮用水源水中的PFAS可能具有相同的污染来源。风险评估结果表明,所有点位饮用水源水中的PFAS不会导致明显的生态风险;饮用水源水中全氟己烷磺酸(PFHxS)、全氟壬酸(PFNA)、六氟环氧丙烷二聚酸(HFPO-DA)和PFBS的水平符合美国国家主要饮用水法规对饮用水中PFAS的限量要求。鉴于传统及新型PFAS在饮用水源水中广泛检出,未来需开展持续跟踪监测活动,以保障居民饮用水安全。

关键词: 全氟和多氟烷基物质, 饮用水源水, 污染特征, 风险评估

Abstract:

Per- and polyfluoroalkyl substances(PFAS) are notorious environmental contaminants that are often referred to as “forever chemicals”. Eastern China is a major region that produces and utilizes PFAS. These substances can enter the environment and migrate to drinking water sources, thereby posing potential ecological and health risks. To investigate the occurrence and potential risks of both legacy and novel PFAS in the drinking water sources of this region, a study was conducted on water samples collected from 13 drinking water sources. Anion exchange solid-phase extraction coupled with ultra performance liquid chromatography-triple quadrupole mass spectrometry(UPLC-MS/MS) was used to determine PFAS in water. The pollution levels and spatial distribution characteristics of 50 legacy and novel PFAS in these drinking water sources were studied in detail and their ecological and health risks were also assessed. Twenty-six types of PFAS were detected in the drinking water sources of the eastern region, with total mass concentrations ranging from 80.0 to 282 ng/L and a median mass concentration of 153 ng/L. The relatively high concentrations of PFAS in these drinking water samples is likely due to heavy industrial activities in this region. Nevertheless, the levels of perfluorooctanoic acid(PFOA) and perfluorooctanesulfonic acid(PFOS) in all sampling sites were far below the limits of national drinking water standards of China. The detected PFAS in drinking water sources were predominantly short-chain compounds, such as perfluorobutanoic acid(PFBA) and perfluorobutanesulfonic acid(PFBS), which accounted for 27.6% and 20.8% of the total PFAS concentration, respectively. In contrast, long-chain PFAS(with more than nine carbons) constituted less than 2% of the total PFAS concentration. The observed higher proportions of short-chain PFAS are rationalized by their somewhat higher mobilities in aquatic environments. Low levels of various novel PFAS, such as hexafluoropropylene oxide dimer acid(HFPO-DA), 1H,1H,2H,2H-perfluorooctanesulfonic acid(6∶2 FTS), perfluoro(2-ethoxyethane)sulfonic acid(PFEESA), 9-chlorohexadecafluoro-3-oxanonane-1-sulfonic acid(9Cl-PF3ONS), and perfluorooctanesulfonamide(FOSA) were detected to varying degrees in the drinking water sources. This indicated that novel PFAS are being increasingly produced and used as alternatives to those restricted by international and Chinese regulations. The overall PFAS pollution levels and compositions in the drinking water sources of Eastern China are significantly influenced by nearby industrial activities, with wastewater discharged from chemical industrial parks and related enterprises contributing significantly to the elevated PFAS levels in the drinking water sources. Pearson correlation analysis suggested that the PFAS in these drinking water sources likely arise from common pollution sources. Ecological risk-assessment data reveal that the PFAS risk quotient in the abovementioned drinking water sources ranged from 9.7×10-6 to 8.9×10-³, which suggests that the PFAS levels at the sampling sites in this study evidently pose no ecological risks. The hazard indices for perfluorohexanoic acid(PFHxS), perfluorononanoic acid(PFNA), HFPO-DA, and PFBS in the examined drinking water sources ranged from 0.16 to 0.89. The detected levels of these four PFAS are compliant with the limits set by the national primary drinking water regulations of the United States. This study furnishes foundational data that provide a comprehensive understanding of the pollution profiles of PFAS in drinking water sources in Eastern China. Continuous monitoring is necessary to ensure drinking-water safety for residents given the widespread occurrence of both legacy and novel PFAS in drinking water.

Key words: per- and polyfluoroalkyl substances(PFAS), drinking water sources, pollution characteristics, risk assessment

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