Non-extractable PFAS in functional textiles – characterization by complementary methods: oxidation, hydrolysis, and fluorine sum parameters†

IF 4.3 3区 环境科学与生态学 Q1 CHEMISTRY, ANALYTICAL Environmental Science: Processes & Impacts Pub Date : 2023-07-12 DOI:10.1039/D3EM00131H
Jonathan Zweigle, Catharina Capitain, Fabian Simon, Philipp Roesch, Boris Bugsel and Christian Zwiener
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Abstract

Per- and polyfluoroalkyl substances (PFAS) are widely used for durable water-repellent finishing of different fabrics and textiles such as outdoor clothing, carpets, medical textiles and more. Existing PFAS extraction techniques followed by target analysis are often insufficient for detecting widely used side-chain fluorinated polymers (SFPs) that are barely or non-extractable. SFPs are typically copolymers consisting of a non-fluorinated backbone with perfluoroalkyl side-chains to obtain desired properties. We compared the accessible analytical information and performance of complementary techniques based on oxidation (dTOP and PhotoTOP assays), hydrolysis (THP assay), standard extraction, extractable organic fluorine (EOF), and total fluorine (TF) with five functional textiles and characterized 7 further textiles only by PhotoTOP oxidation. The results show that when applied directly to textile samples, dTOP and PhotoTOP oxidation and also hydrolysis (THP) are able to capture large fractions of TF in the form of perfluoroalkyl side-chains present in the textiles while methods relying on extracts (EOF, target and non-target analysis) yield much lower fractions of TF (e.g., factor ∼25–50 lower). The conversion of large fractions of the measured TF into PFCAs or FTOHs from fluorinated side chains is in contrast to previous studies. Concentrations ranged from <LOQ to over ∼1000 mg F kg−1 after oxidation/hydrolysis and <LOQ to over 2000 mg F kg−1 for TF, while EOF and target PFAS in extracts were detected at much lower concentrations (up to ∼60 mg F kg−1) (amount of fluorine is in the order: extraction ≪ EOF ≪ oxidation/hydrolysis ≤ TF). Perfluoroalkyl carboxylic acids (PFCAs) and fluorotelomer alcohols (FTOHs) from THP hydrolysis and PhotoTOP oxidation both represented chain-length distribution in the textiles showing that long-chain SFPs are still used in current textiles. Further advantages and disadvantages of the applied methods are discussed.

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功能性纺织品中不可提取的PFAS -通过互补方法表征:氧化,水解和氟求和参数†
全氟和多氟烷基物质(PFAS)广泛用于各种织物和纺织品的耐用防水整理,如户外服装、地毯、医用纺织品等。现有的PFAS提取技术,然后进行目标分析,往往不足以检测广泛使用的侧链氟化聚合物(SFPs),这些聚合物几乎不可提取或不可提取。SFPs通常是由非氟化主链与全氟烷基侧链组成的共聚物,以获得所需的性能。我们比较了基于氧化(dTOP和PhotoTOP法)、水解(THP法)、标准萃取、可提取有机氟(EOF)和总氟(TF)的互补技术对5种功能性纺织品的分析信息和性能,并对另外7种纺织品进行了仅用PhotoTOP法氧化的表征。结果表明,当直接应用于纺织品样品时,dTOP和PhotoTOP氧化以及水解(THP)能够以纺织品中存在的全氟烷基侧链的形式捕获大部分TF,而依赖于提取物(EOF,目标和非目标分析)的方法产生的TF含量要低得多(例如,低25-50倍)。从氟化侧链上将大量测得的TF转化为PFCAs或FTOHs与先前的研究相反。氧化/水解后的LOQ范围为- 1000 mg F kg - 1以上,TF的LOQ范围为- 2000 mg F kg - 1以上,而提取液中EOF和目标PFAS的检测浓度要低得多(高达- 60 mg F kg - 1)(氟含量顺序为:提取液≪EOF≪氧化/水解≤TF)。来自THP水解和PhotoTOP氧化的全氟烷基羧酸(PFCAs)和氟端聚物醇(FTOHs)都代表了纺织品中的链长分布,表明长链SFPs仍在当前纺织品中使用。进一步讨论了所采用方法的优缺点。
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来源期刊
Environmental Science: Processes & Impacts
Environmental Science: Processes & Impacts CHEMISTRY, ANALYTICAL-ENVIRONMENTAL SCIENCES
CiteScore
9.50
自引率
3.60%
发文量
202
审稿时长
1 months
期刊介绍: Environmental Science: Processes & Impacts publishes high quality papers in all areas of the environmental chemical sciences, including chemistry of the air, water, soil and sediment. We welcome studies on the environmental fate and effects of anthropogenic and naturally occurring contaminants, both chemical and microbiological, as well as related natural element cycling processes.
期刊最新文献
Correction: Exploring the variability of PFAS in urban sewage: a comparison of emissions in commercial versus municipal urban areas. Validation of a laboratory spray generation system and its use in a comparative study of hexamethylene diisocyanate (HDI) evaluation methods. Fluorinated aromatic PBCTF and 6:2 diPAP in bridge and traffic paints. Sorption of metal ions onto PET-derived microplastic fibres. Reduction of hexavalent chromium by compost-derived dissolved organic matter.
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