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污水污泥和住宅泵站中全氟烷基和多氟烷基物质前体含量升高。

Elevated PFAS Precursors in Septage and Residential Pump Stations.

作者信息

Penrose Michael, Deighton Jacob, Glassmeyer Susan T, Brougham Andrew, Bessler Scott M, Mcknight Taryn, Ateia Mohamed

机构信息

ORISE Participant at Center for Environmental Solutions & Emergency Response, U.S. Environmental Protection Agency, Cincinnati, Ohio 45220, United States.

Metropolitan Sewer District of Greater Cincinnati, Cincinnati, Ohio 45204, United States.

出版信息

Environ Sci Technol Lett. 2025 Mar 25;12(4):454-460. doi: 10.1021/acs.estlett.5c00246.

Abstract

Residential wastewater, with no industrial inputs, is an underrecognized source of per- and polyfluoroalkyl substances (PFAS). This study provides the first direct comparison of PFAS in septage and pump stations, targeting 70 PFAS compounds and employing the total oxidizable precursor (TOP) assay. Septage exhibited markedly higher PFAS and precursors concentrations than pump stations, with median post-TOP levels of 687.5 ng/L vs 84.2 ng/L, respectively. FTCAs were fully oxidized, while diPAPs showed incomplete oxidation due to high organic loads. Septic systems function as PFAS reservoirs, increasing risks of groundwater contamination, particularly in areas with shallow aquifers. Pump stations contributed to episodic PFAS spikes, likely affecting downstream wastewater treatment. The detection of 27 PFAS compounds, including short-chain alternatives, highlights shifting contamination patterns. Findings emphasize the need for tailored analytical frameworks and pretreatment technologies to mitigate PFAS risks across decentralized and centralized wastewater systems. Integrating precursor analysis is critical for accurate risk assessment, as targeted PFAS measurements underestimate contamination. These results provide new insights into PFAS behavior in residential wastewater, guiding future mitigation efforts.

摘要

没有工业排放的生活污水是一种未得到充分认识的全氟和多氟烷基物质(PFAS)来源。本研究首次对化粪池污水和泵站中的PFAS进行了直接比较,针对70种PFAS化合物并采用总可氧化前体(TOP)分析法。化粪池污水中的PFAS和前体浓度明显高于泵站,TOP分析后的中位数水平分别为687.5 ng/L和84.2 ng/L。全氟三羧酸(FTCAs)被完全氧化,而二聚全氟辛烷磺酸(diPAPs)由于有机负荷高而显示出不完全氧化。化粪池系统充当PFAS的储存库,增加了地下水污染的风险,特别是在浅层含水层地区。泵站导致PFAS出现间歇性峰值,可能影响下游污水处理。检测到27种PFAS化合物,包括短链替代品,突出了污染模式的变化。研究结果强调需要有针对性的分析框架和预处理技术,以降低分散式和集中式废水系统中的PFAS风险。整合前体分析对于准确的风险评估至关重要,因为针对PFAS的测量会低估污染程度。这些结果为PFAS在生活污水中的行为提供了新的见解,指导未来的缓解措施。

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