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微塑料和全氟辛烷磺酸的气-水相互作用与沉积。

Microplastics and PFAS air-water interaction and deposition.

作者信息

Wang Yuxin, Good Kelly D

机构信息

Systems Science and Industrial Engineering, State University of New York at Binghamton, United States of America.

Civil and Environmental Engineering, Villanova University, United States of America.

出版信息

Sci Total Environ. 2024 Dec 1;954:176247. doi: 10.1016/j.scitotenv.2024.176247. Epub 2024 Sep 12.

DOI:10.1016/j.scitotenv.2024.176247
PMID:39277013
Abstract

Although microplastics (MPs) and per- and polyfluoroalkyl substances (PFAS) have received tremendous attention separately, understanding their ubiquitous presence in the environment, persistence and toxicity requires comprehensive study of the fate and transport of co-existing MPs and PFAS. MPs may have large sorption capacity and can serve as vectors for PFAS to undergo long-range transport in water. Atmospheric deposition of both PFAS and MPs has been reported in urban, rural, and remote areas. This review identifies types and levels of PFAS and MPs in air, their interactions, and environmental factors contributing to their air-water deposition. MPs in combination with PFAS may carry combined toxicity and pose elevated risks to ecosystems and human health. Our review shows that air-water deposition of MPs and PFAS can be governed by environmental factors including precipitation, humidity, UV, wind, and particulate matter levels in the air. Increasing humidity may increase MP particle size due to hygroscopic growth, which affects its distribution and deposition rate. Humidity has been observed to have both positive and negative impacts on PFAS partitioning onto MPs. More attention should be paid to MPs and PFAS co-occurrence when addressing their transport behavior in air and deposition to aquatic systems.

摘要

尽管微塑料(MPs)和全氟及多氟烷基物质(PFAS)已分别受到广泛关注,但要了解它们在环境中的普遍存在、持久性和毒性,需要对共存的微塑料和全氟及多氟烷基物质的归宿和迁移进行全面研究。微塑料可能具有较大的吸附能力,并可作为全氟及多氟烷基物质在水中进行长距离迁移的载体。在城市、农村和偏远地区均已报道了全氟及多氟烷基物质和微塑料的大气沉降。本综述确定了空气中全氟及多氟烷基物质和微塑料的类型和水平、它们之间的相互作用以及导致它们进行空气-水沉降的环境因素。微塑料与全氟及多氟烷基物质结合可能具有联合毒性,并对生态系统和人类健康构成更高风险。我们的综述表明,微塑料和全氟及多氟烷基物质的空气-水沉降可能受包括降水、湿度、紫外线、风以及空气中颗粒物水平等环境因素的影响。湿度增加可能会由于吸湿增长而增加微塑料颗粒大小,这会影响其分布和沉降速率。已观察到湿度对全氟及多氟烷基物质在微塑料上的分配既有正面影响也有负面影响。在研究它们在空气中的迁移行为以及向水生系统的沉降时,应更加关注微塑料和全氟及多氟烷基物质的共存情况。

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