Multifunctionalized Covalent Organic Frameworks for Broad-Spectrum Extraction and Ultrasensitive Analysis of Per- and Polyfluoroalkyl Substances

化学 阳离子聚合 萃取(化学) 复矩阵 检出限 色谱法 固相萃取 广谱 环境化学 组合化学 有机化学
作者
Chenchen Song,Juan Zheng,Qidong Zhang,Hang Yuan,Ajuan Yu,Wenfen Zhang,Shusheng Zhang,Gangfeng Ouyang
出处
期刊:Analytical Chemistry [American Chemical Society]
卷期号:95 (19): 7770-7778 被引量:27
标识
DOI:10.1021/acs.analchem.3c01137
摘要

The contamination of surface and ground water by per- and polyfluoroalkyl substances (PFASs) has become a growing concern, and the structural diversity of PFASs is the major challenge for their ubiquitous applications. Strategies for monitoring coexistent anionic, cationic, and zwitterionic PFASs even at trace levels in aquatic environments are urgently demanded for effective pollution control. Herein, novel amide group and perfluoroalkyl chain-functionalized covalent organic frameworks (COFs) named COF-NH-CO-F9 are successfully synthesized and used for highly efficient extraction of broad-spectrum PFASs, attributing to their unique structure and the multifunctional groups. Under the optimal conditions, a simple and high-sensitivity method is established to quantify 14 PFASs including anionic, cationic, and zwitterionic species by coupling solid-phase microextraction (SPME) with ultrahigh-performance liquid chromatography–triple quadrupole mass spectrometry (UHPLC-MS/MS) for the first time. The established method displays high enrichment factors (EFs) of 66–160, ultrahigh sensitivity with low limits of detection (LODs) of 0.0035–0.18 ng L–1, a wide linearity of 0.1–2000 ng L–1 with correlation coefficient (R2) ≥0.9925, and satisfactory precision with relative standard deviations (RSDs) ≤11.2%. The excellent performance is validated in real water samples with recoveries of 77.1–108% and RSDs ≤11.4%. This work highlights the potential of rational design of COFs with the desired structure and functionality for the broad-spectrum enrichment and ultrasensitive determination of PFASs in real applications.
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