长江下游饮用水系统中的全氟和多氟烷基物质(PFAS):来源、归宿和健康风险评估

IF 3.2 3区 环境科学与生态学 Q3 ENGINEERING, ENVIRONMENTAL
Yuan Hong, Qin Ding, Tingting Yang, Xiaoqin Li, Ninghui Song, Juan Zhang
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引用次数: 0

摘要

长江受到中国全氟烷基和多氟烷基物质(PFAS)相关工业活动的严重影响,对饮用水安全构成潜在威胁。到目前为止,我们对河流中PFAS的发生及其在整个饮用水供应系统中的命运的了解仍然有限。采用目标筛选法对江苏省饮用水系统中PFAS进行了全面调查。在整个处理过程水流、源水和家庭自来水中检测到12种全氟烷基酸(PFAAs)和7种新出现的全氟烷基酸(PFAS),并进行了精确量化,浓度为61.34 ~ 90.40 ng/L。PFAAs [PFOA (30.26 ng/L)、PFBS (23.25 ng/L)、PFBA (18.82 ng/L)和PFHxA (16.89 ng/L)]和8:8 pffia (13.63 ng/L)是长江下游的优势污染物。自来水中主要污染物为PFBA (19.92 ng/L)、PFBS (15.02 ng/L)和PFOA (11.94 ng/L)。粉状活性炭在DWTP-B中预处理后,对长链PFAS的去除率为21.36 ~ 65.84%,对PFOA的去除率最高。臭氧氧化对新出现的PFAS的去除率为3.22 ~ 11.06%,但PFAAs浓度有所增加。颗粒活性炭过滤对长链PFAS的去除效果较好,其中DWTP-B的效果优于DWTP-A。pfsa(3.12 ~ 22.09%)的去除率优于PFCAs(- 0.62 ~ 19.54%)。婴儿和儿童通过饮用水摄入PFAS面临中等健康风险,在9个月至1岁年龄组达到峰值(HQ = 2.45)。这些发现强调了改进PFAS去除技术和严格监管PFAS污染的必要性,以减少长江PFAS污染。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Per- and polyfluoroalkyl substances (PFAS) in drinking water systems in the lower Yangtze River: source, fate, and health risk assessment.

The Yangtze River is significantly impacted by industrial activities related to per- and polyfluoroalkyl substances (PFAS) in China, posing potential threats to drinking water safety. So far, our knowledge of PFAS occurrence in the river and their fate in the whole drinking water supply systems remains limited. We conducted a comprehensive investigation of PFAS in Jiangsu's drinking water systems, using the target screening method. 12 perfluoroalkyl acids (PFAAs) and 7 emerging PFAS were detected and precisely quantified in the whole treatment process water flows, as well as source water and household tap water with concentrations of 61.34-90.40 ng/L. PFAAs [PFOA (30.26 ng/L), PFBS (23.25 ng/L), PFBA (18.82 ng/L) and PFHxA (16.89 ng/L)] and 8:8 PFPiA (13.63 ng/L) were the dominant pollutants in the low Yangtze River. PFBA (19.92 ng/L), PFBS (15.02 ng/L) and PFOA (11.94 ng/L) were major contaminants in tap water. The powder activated carbon pre-treatment in DWTP-B could remove 21.36-65.84% of long-chain PFAS, especially PFOA. Ozonation achieved slight emerging PFAS removal (3.22-11.06%), while PFAAs concentrations exhibited an increase. Granular active carbon filtration was effective in removing long-chain PFAS, with DWTP-B outperforming DWTP-A. PFSAs (3.12-22.09%) had a better removal than PFCAs (- 0.62 to 19.54%). Infants and children face a moderate health risk of PFAS intake through drinking water, peaking at the age group of 9 months to 1 year (HQ = 2.45). These findings underscore the necessity for improved PFAS removal technologies and stricter regulation of PFAS contamination in the Yangtze River to reduce exposure.

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来源期刊
Environmental Geochemistry and Health
Environmental Geochemistry and Health 环境科学-工程:环境
CiteScore
8.00
自引率
4.80%
发文量
279
审稿时长
4.2 months
期刊介绍: Environmental Geochemistry and Health publishes original research papers and review papers across the broad field of environmental geochemistry. Environmental geochemistry and health establishes and explains links between the natural or disturbed chemical composition of the earth’s surface and the health of plants, animals and people. Beneficial elements regulate or promote enzymatic and hormonal activity whereas other elements may be toxic. Bedrock geochemistry controls the composition of soil and hence that of water and vegetation. Environmental issues, such as pollution, arising from the extraction and use of mineral resources, are discussed. The effects of contaminants introduced into the earth’s geochemical systems are examined. Geochemical surveys of soil, water and plants show how major and trace elements are distributed geographically. Associated epidemiological studies reveal the possibility of causal links between the natural or disturbed geochemical environment and disease. Experimental research illuminates the nature or consequences of natural or disturbed geochemical processes. The journal particularly welcomes novel research linking environmental geochemistry and health issues on such topics as: heavy metals (including mercury), persistent organic pollutants (POPs), and mixed chemicals emitted through human activities, such as uncontrolled recycling of electronic-waste; waste recycling; surface-atmospheric interaction processes (natural and anthropogenic emissions, vertical transport, deposition, and physical-chemical interaction) of gases and aerosols; phytoremediation/restoration of contaminated sites; food contamination and safety; environmental effects of medicines; effects and toxicity of mixed pollutants; speciation of heavy metals/metalloids; effects of mining; disturbed geochemistry from human behavior, natural or man-made hazards; particle and nanoparticle toxicology; risk and the vulnerability of populations, etc.
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