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混合模式色谱法在同时分析 C-C 型全氟烷基物质中的适用性。

Applicability of mixed-mode chromatography for the simultaneous analysis of C-C perfluoroalkylated substances.

机构信息

Department of Analytical Chemistry, Nutrition and Food Sciences, IIAA - Institute for Food Analysis and Research, Universidade de Santiago de Compostela, Constantino Candeira S/N, 15782, Santiago de Compostela, Spain.

出版信息

Anal Bioanal Chem. 2020 Aug;412(20):4849-4856. doi: 10.1007/s00216-020-02434-w. Epub 2020 Jan 31.

Abstract

A new analytical method for the determination of 22 perfluoroalkylated (carboxylic and sulfonic) acids in water samples is presented. The method's objective was to achieve the simultaneous quantification of compounds with different chain lengths (from C to C). To this end, 500 mL of water were extracted with Oasis WAX solid-phase extraction cartridges and eluted with 3 mL of 5% ammonia in methanol. After evaporation to dryness, extracts were reconstituted in methanol:ultrapure water (1:1) and analyzed by mixed-mode liquid chromatography-tandem mass spectrometry (MMLC-MS/MS) using a weak anion exchange/reversed-phase column. The method provided good results, with limits of quantification lower than 1 ng/L in river water for most of compounds, except the two perfluorocarboxylic acids with the longest alkyl chain (>C) and trifluoroacetic acid, for which a blank contamination problem was observed. The method proved good trueness and precision in both ultrapure and river water (R ≥ 81%, RSD ≤ 15%). After validation, the method was applied to the analysis of nine water samples where nine perfluoroalkylated acids were quantified. Seven of them were ultrashort- (C-C) and short-chain (C-C) perfluoroalkylated acids, pointing out the importance of developing methods capable to target such substances for further monitoring.

摘要

一种新的用于测定水样中 22 种全氟烷基化(羧酸和磺酸)酸的分析方法。该方法的目的是实现对不同链长(从 C 到 C)化合物的同时定量。为此,将 500 毫升水用 Oasis WAX 固相萃取小柱萃取,并用 3 毫升 5%氨甲醇洗脱。蒸发至干后,将提取物用甲醇:超纯水(1:1)重新溶解,并通过混合模式液相色谱-串联质谱(MMLC-MS/MS)进行分析,使用弱阴离子交换/反相柱。该方法取得了良好的结果,对于大多数化合物,除了两种最长链烷基(>C)的全氟羧酸和三氟乙酸外,河水中的定量限均低于 1 ng/L,对于这两种化合物,观察到空白污染问题。该方法在超纯水和河水(R≥81%,RSD≤15%)中均表现出良好的准确度和精密度。验证后,该方法应用于九种水样的分析,定量了九种全氟烷基酸。其中七种为超短链(C-C)和短链(C-C)全氟烷基酸,这表明开发能够针对此类物质进行进一步监测的方法非常重要。

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