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中空纤维液相微萃取结合超临界流体色谱-质谱联用技术用于水样中多类新兴污染物的定量分析。

Hollow fiber liquid-phase microextraction combined with supercritical fluid chromatography coupled to mass spectrometry for multiclass emerging contaminant quantification in water samples.

机构信息

Facultad de Ciencias Químicas, Universidad de Colima, Carretera Colima-Coquimatlán km 9, 28400, Coquimatlán, Colima, Mexico.

Facultad de Ciencias, Universidad de Colima, c/ Bernal Díaz del Castillo 340, 28045, Colima, Mexico.

出版信息

Anal Bioanal Chem. 2021 Apr;413(9):2467-2479. doi: 10.1007/s00216-021-03202-0. Epub 2021 Feb 3.

DOI:10.1007/s00216-021-03202-0
PMID:33532915
Abstract

The hollow fiber liquid-phase microextraction allows highly selective concentration of organic compounds that are at trace levels. The determination of those analytes through the supercritical fluid chromatography usage is associated with many analytical benefits, which are significantly increased when it is coupled to a mass spectrometry detector, thus providing an extremely sensitive analytical technique with minimal consumption of organic solvents. On account of this, a hollow fiber liquid-phase microextraction technique in two-phase mode combined with supercritical fluid chromatography coupled to mass spectrometry was developed for quantifying 19 multiclass emerging contaminants in water samples in a total chromatographic time of 5.5 min. The analytical method used 40 μL of 1-octanol placed in the porous-walled polypropylene fiber as the acceptor phase, and 1 L of water sample was the donor phase. After extraction and quantification techniques were optimized in detail, a good determination coefficient (r > 0.9905) in the range of 0.1 to 100 μg L, for most of the analytes, and an enrichment factor in the range of 7 to 28,985 were obtained. The recovery percentage (%R) and intraday precision (%RSD) were in the range of 80.80-123.40%, and from 0.48 to 16.89%, respectively. Limit of detection and quantification ranged from 1.90 to 35.66 ng L, and from 3.41 to 62.11 ng L, respectively. Finally, the developed method was successfully used for the determination of the 19 multiclass emerging contaminants in superficial and wastewater samples.

摘要

中空纤维液相微萃取允许对痕量水平的有机化合物进行高度选择性的浓缩。通过超临界流体色谱的使用来测定这些分析物与许多分析优势相关联,当与质谱检测器耦合时,这些优势会显著增加,从而提供一种极其灵敏的分析技术,有机溶剂的消耗量最小。因此,开发了一种两相模式的中空纤维液相微萃取技术与超临界流体色谱-质谱联用,用于在 5.5 分钟的总色谱时间内定量测定水样中的 19 种多类新兴污染物。该分析方法使用 40μL 置于多孔壁聚丙烯纤维中的 1-辛醇作为接受相,1L 水样作为供体相。在详细优化了萃取和定量技术后,对于大多数分析物,在 0.1 至 100μg L 的范围内获得了良好的测定系数(r>0.9905)和 7 至 28985 的富集因子。回收率(%R)和日内精密度(%RSD)分别在 80.80-123.40%和 0.48-16.89%的范围内。检出限和定量限范围分别为 1.90 至 35.66ng L 和 3.41 至 62.11ng L。最后,该方法成功用于测定地表和废水样品中的 19 种多类新兴污染物。

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本文引用的文献

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A rapid method for quantification of persistent and mobile organic substances in water using supercritical fluid chromatography coupled to high-resolution mass spectrometry.使用超临界流体色谱与高分辨质谱联用快速定量水中的持久性和可移动有机物质。
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Supercritical fluid chromatography-a technical overview and its applications in medicinal plant analysis: an update covering 2012-2018.超临界流体色谱技术概述及其在药用植物分析中的应用:2012-2018 年的更新综述。
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Simultaneous determination of multiresidue and multiclass emerging contaminants in waters by rotating-disk sorptive extraction-derivatization-gas chromatography/mass spectrometry.旋转盘吸附萃取-衍生化-气相色谱/质谱法同时测定水中多种残留和多类新兴污染物
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Solid phase extraction of pesticides from environmental waters using an MSU-1 mesoporous material and determination by UPLC-MS/MS.使用MSU-1介孔材料从环境水样中固相萃取农药并通过超高效液相色谱-串联质谱法测定
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