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用于水体中极性有机微量污染物的化合物特异性同位素分析的分子印迹聚合物。

Molecularly Imprinted Polymers for Compound-Specific Isotope Analysis of Polar Organic Micropollutants in Aquatic Environments.

机构信息

Eawag , Swiss Federal Institute of Aquatic Science and Technology , CH-8600 Dübendorf , Switzerland.

Institute of Biogeochemistry and Pollutant Dynamics , ETH Zürich , CH-8092 Zürich , Switzerland.

出版信息

Anal Chem. 2018 Jun 19;90(12):7292-7301. doi: 10.1021/acs.analchem.8b00493. Epub 2018 Jun 4.

DOI:10.1021/acs.analchem.8b00493
PMID:29779374
Abstract

Compound-specific isotope analysis (CSIA) of polar organic micropollutants in environmental waters requires a processing of large sample volumes to obtain the required analyte masses for analysis by gas chromatography/isotope-ratio mass spectrometry (GC/IRMS). However, the accumulation of organic matter of unknown isotopic composition in standard enrichment procedures currently compromises the accurate determination of isotope ratios. We explored the use of molecularly imprinted polymers (MIPs) for selective analyte enrichment for C/C and N/N ratio measurements by GC/IRMS using 1 H-benzotriazole, a typical corrosion inhibitor in dishwashing detergents, as example of a widely detected polar organic micropollutant. We developed procedures for the treatment of >10 L of water samples, in which custom-made MIPs enabled the selective cleanup of enriched analytes in organic solvents obtained through conventional solid-phase extractions. Hydrogen bonding interactions between the triazole moiety of 1 H-benzotriazole, and the MIP were responsible for selective interactions through an assessment of interaction enthalpies and N isotope effects. The procedure was applied successfully without causing isotope fractionation to river water samples, as well as in- and effluents of wastewater treatment plants containing μg/L concentrations of 1 H-benzotriazole and dissolved organic carbon (DOC) loads of up to 28 mg C/L. MIP-based treatments offer new perspectives for CSIA of organic micropollutants through the reduction of the DOC-to-micropollutant ratios.

摘要

环境水中的极性有机微量污染物的化合物特异性同位素分析(CSIA)需要处理大量的样品体积,以获得通过气相色谱/同位素-比质谱(GC/IRMS)分析所需的分析物质量。然而,目前在标准富集程序中积累的未知同位素组成的有机物会影响同位素比的准确测定。我们探索了使用分子印迹聚合物(MIPs)进行选择性分析物富集,用于通过 GC/IRMS 进行 C/C 和 N/N 比测量,以 1H-苯并三唑(一种典型的洗碗洗涤剂中的腐蚀抑制剂)为例,作为广泛检测到的极性有机微量污染物的例子。我们开发了处理超过 10 L 水样的程序,其中定制的 MIPs 能够在通过常规固相萃取获得的有机溶剂中选择性地净化富集的分析物。1H-苯并三唑的三唑部分与 MIP 之间的氢键相互作用,通过评估相互作用焓和 N 同位素效应,负责选择性相互作用。该程序成功地应用于河水样品,以及含有μg/L 浓度的 1H-苯并三唑和高达 28mg C/L 的溶解有机碳(DOC)负荷的污水处理厂的进水和出水,而不会引起同位素分馏。基于 MIP 的处理方法通过降低 DOC-与微量污染物的比例,为有机微量污染物的 CSIA 提供了新的视角。

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