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

被引:8
作者
del Carmen Salvatierra-Stamp, Vilma [1 ]
Ceballos-Magana, Silvia G. [2 ]
Susana Pano-Farias, Norma [3 ]
Belisario Leyva-Morales, Jose [4 ]
Pineda-Urbina, Kayim [1 ]
Muniz-Valencia, Roberto [1 ]
机构
[1] Univ Colima, Fac Ciencias Quim, Carretera Colima Coquimatlan Km 9, Colima 28400, Mexico
[2] Univ Colima, Fac Ciencias, C Bernal Diaz del Castillo 340, Colima 28045, Mexico
[3] CIDAM AC, Ctr Innovac & Desarrollo Agroalimentario Michoaca, Antigua Carretera Patzcuaro Km 8, Morelia 58341, Michoacan, Mexico
[4] Univ Autonoma Occidente, Dept Salud, Unidad Guasave, Av Univ S-N, Guasave 81044, Sinaloa, Mexico
关键词
Multiclass emerging contaminants; Hollow fiber liquid-phase microextraction; Supercritical fluid chromatography; Water samples; EXTRACTION; EFFICIENCY;
D O I
10.1007/s00216-021-03202-0
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
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 mu L 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(2) > 0.9905) in the range of 0.1 to 100 mu g L-1, 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-1, and from 3.41 to 62.11 ng L-1, respectively. Finally, the developed method was successfully used for the determination of the 19 multiclass emerging contaminants in superficial and wastewater samples.
引用
收藏
页码:2467 / 2479
页数:13
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