Biotransformation of AFFF Component 6:2 Fluorotelomer Thioether Amido Sulfonate Generates 6:2 Fluorotelomer Thioether Carboxylate under Sulfate-Reducing Conditions

硫醚 生物转化 化学 微观世界 硫酸盐 羧酸盐 生物降解 磺酸盐 硫黄 硫化物 有机化学 环境化学 色谱法
作者
Shan Yi,Katie C. Harding-Marjanovic,Erika Houtz,Ying Gao,Jennifer E. Lawrence,R.V. Nichiporuk,Anthony T. Iavarone,Wei‐Qin Zhuang,Martin Hansen,Jennifer A. Field,David L. Sedlak,Lisa Alvarez‐Cohen
出处
期刊:Environmental Science and Technology Letters [American Chemical Society]
卷期号:5 (5): 283-288 被引量:74
标识
DOI:10.1021/acs.estlett.8b00148
摘要

The fate of per and polyfluoroalkyl substances (PFASs) in aqueous filmforming foams (AFFFs) under anaerobic conditions has not been well characterized, leaving major gaps in our understanding of PFAS fate and transformation at contaminated sites. In this study, the biotransformation of 6:2 fluorotelomer thioether amido sulfonate (6:2 FtTAoS), a component of several AFFF formulations, was investigated under sulfate-reducing conditions in microcosms inoculated with either pristine or AFFF-impacted solids. To identify the transformation products, we used high-resolution mass spectrometry and employed suspect-screening and nontargeted compound identification methods. These analyses demonstrated that 6:2 FtTAoS was transformed primarily to a stable polyfluoroalkyl compound, 6:2 fluorotelomer thioether propionate (6:2 FtTP). It did not undergo further reactions to produce the perfluoroalkyl carboxylates and fluorotelomer sulfonates and carboxylates that were observed during aerobic transformations. Here, the 6:2 FtTP was recalcitrant to biotransformation, indicating the stability of the thioether group under sulfate reducing conditions. The total oxidizable precursor (TOP) assay was used to assess the presence of other PFASs. Although nearly all of the PFAS mass initially present was recovered from the pristine microcosms, only 67% of the initial PFAS mass was recovered from the contaminated microcosms, suggesting the formation of volatile biotransformation products or those that could not be detected by the TOP assay.
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