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全氟和多氟烷基物质替代品的未竟之述:水生环境中替代品的赋存、生态毒理学影响及去除策略的研究进展。

The untold story of PFAS alternatives: Insights into the occurrence, ecotoxicological impacts, and removal strategies in the aquatic environment.

机构信息

Faculty of Science and Marine Environment, Universiti Malaysia Terengganu, 21030 Kuala Nerus, Terengganu, Malaysia; Ocean Pollution and Ecotoxicology (OPEC) Research Group, Universiti Malaysia Terengganu, Malaysia.

College of Marine Sciences, South China Agricultural University, Guangzhou 510641, China.

出版信息

Water Res. 2024 Feb 15;250:121044. doi: 10.1016/j.watres.2023.121044. Epub 2023 Dec 23.

Abstract

Due to increasing regulations on the production and consumption of legacy per- and polyfluoroalkyl substances (PFAS), the global use of PFAS substitutes increased tremendously, posing serious environmental risks owing to their bioaccumulation, toxicity, and lack of removal strategies. This review summarized the spatial distribution of alternative PFAS and their ecological risks in global freshwater and marine ecosystems. Further, toxicological effects of novel PFAS in various freshwater and marine species were highlighted. Moreover, degradation mechanisms for alternative PFAS removal from aquatic environments were compared and discussed. The spatial distribution showed that 6:2 chlorinated polyfluorinated ether sulfonate (6:2 CI-PFAES, also known as F-53B) was the most dominant emerging PFAS found in freshwater. Additionally, the highest levels of PFBS and PFBA were observed in marine waters (West Pacific Ocean). Moreover, short-chain PFAS exhibited higher concentrations than long-chain congeners. The ecological risk quotients (RQs) for phytoplankton were relatively higher >1 than invertebrates, indicating a higher risk for freshwater phytoplankton species. Similarly, in marine water, the majority of PFAS substitutes exhibited negligible risk for invertebrates and fish, and posed elevated risks for phytoplanktons. Reviewed studies showed that alternative PFAS undergo bioaccumulation and cause deleterious effects such as oxidative stress, hepatoxicity, neurotoxicity, histopathological alterations, behavioral and growth abnormalities, reproductive toxicity and metabolism defects in freshwater and marine species. Regarding PFAS treatment methods, photodegradation, photocatalysis, and adsorption showed promising degradation approaches with efficiencies as high as 90%. Finally, research gaps and future perspectives for alternative PFAS toxicological implications and their removal were offered.

摘要

由于对传统全氟和多氟烷基物质 (PFAS) 的生产和消费的监管日益加强,PFAS 替代品在全球范围内的使用量大幅增加,由于其生物累积性、毒性和缺乏去除策略,对环境构成了严重的风险。本综述总结了全球淡水和海洋生态系统中替代 PFAS 的空间分布及其生态风险。此外,还强调了新型 PFAS 对各种淡水和海洋物种的毒理学影响。此外,还比较和讨论了替代 PFAS 从水生环境中去除的降解机制。空间分布表明,6:2 氯代全氟醚磺酸(6:2 CI-PFAES,也称为 F-53B)是在淡水中发现的最主要的新兴 PFAS。此外,在海洋水中观察到 PFBS 和 PFBA 的最高水平。此外,短链 PFAS 的浓度高于长链同系物。浮游植物的生态风险商 (RQ) 相对较高 (>1),表明淡水浮游植物物种的风险更高。同样,在海水中,大多数 PFAS 替代品对无脊椎动物和鱼类的风险可忽略不计,对浮游植物的风险较高。综述研究表明,替代 PFAS 会发生生物累积,并对淡水和海洋物种造成有害影响,如氧化应激、肝毒性、神经毒性、组织病理学改变、行为和生长异常、生殖毒性和代谢缺陷。关于 PFAS 的处理方法,光降解、光催化和吸附显示出有前途的降解方法,效率高达 90%。最后,提出了替代 PFAS 毒理学影响及其去除的研究空白和未来展望。

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