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模拟太阳光下垃圾渗滤液中 6:2 氟代磺酸盐的间接光解研究:腐殖酸和硝酸盐的影响。

Exploring indirect photolysis of 6:2 fluorotelomer sulfonate in landfill leachate under simulated sunlight: effect of humic acid and nitrate.

机构信息

Civil Engineering, University of British Columbia, 6250 Applied Science Lane, Vancouver, BC, V6T 1Z4, Canada.

Chemical and Biological Engineering, University of British Columbia, 2360 East Mall, Vancouver, BC, V6T 1Z3, Canada.

出版信息

Environ Sci Pollut Res Int. 2021 Feb;28(8):9508-9516. doi: 10.1007/s11356-020-11417-4. Epub 2020 Nov 4.

Abstract

Landfill leachate is exposed to sunlight through on- and off-site leachate treatment and disposal to surface water bodies. Very little is known about the potential phototransformation of fluorotelomer compounds in landfill leachates, which can undergo environmental oxidation and produce perfluorocarboxylic acids (PFCAs). This study investigated phototransformation of spiked 6:2 fluorotelomer sulfonate (FTS) (∼ 100 μg/L) in leachate under simulated sunlight, using a metal halide lamp (wavelength, 390 to 750 nm). To understand the effects of nitrate and humic acid (HA), phosphate buffer (pH 7.1) containing nitrate and HA were spiked with 6:2 FTS and irradiated under simulated sunlight for 72 h. Following irradiation, 6:2 FTS and known transformation products (i.e., PFCAs) were quantified in the samples using LC-MS/MS. The results showed that 6:2 FTS was undergoing indirect photolysis in leachate (half-life of ∼ 15 days), suggesting that indirect photolysis of 6:2 FTS is likely a relevant transformation pathway in sunlit aquatic environments. However, the spiked 6:2 FTS did not show any observable decrease in the presence of nitrate and HA over 72 h. Perfluorohexanoic acid (PFHxA) increased in irradiated leachate background samples (without 6:2 FTS spike) suggesting that phototransformation in sunlit leachate could lead to the formation of persistent PFCAs at environmental concentrations of the precursors. Future studies using probe compounds are recommended to better understand the roles of reactive species in phototransformation of 6:2 FTS.

摘要

垃圾渗滤液通过现场和场外渗滤液处理和处置暴露在阳光下,进而进入地表水。对于垃圾渗滤液中氟调聚物化合物的潜在光转化,人们知之甚少,这些化合物可能会经历环境氧化并产生全氟羧酸(PFCAs)。本研究使用金属卤化物灯(波长 390 至 750nm),在模拟阳光条件下研究了渗滤液中添加的 6:2 氟调聚磺酸盐(FTS)(∼100μg/L)的光转化。为了了解硝酸盐和腐殖酸(HA)的影响,在含有硝酸盐和 HA 的磷酸盐缓冲液(pH7.1)中添加了 6:2 FTS,并在模拟阳光照射下辐照 72 小时。辐照后,使用 LC-MS/MS 定量测定样品中的 6:2 FTS 和已知转化产物(即 PFCAs)。结果表明,6:2 FTS 在渗滤液中经历间接光解(半衰期约为 15 天),这表明 6:2 FTS 的间接光解可能是阳光充足的水生环境中的一种相关转化途径。然而,在 72 小时内,添加的 6:2 FTS 在硝酸盐和 HA 的存在下没有表现出任何可观察到的减少。在辐照的渗滤液背景样品(无 6:2 FTS 添加)中,全氟己酸(PFHxA)增加,这表明阳光充足的渗滤液中的光转化可能导致在环境浓度的前体物下形成持久性的 PFCAs。建议使用探针化合物进行未来的研究,以更好地了解活性物质在 6:2 FTS 光转化中的作用。

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