Improved solid-phase microextraction extraction procedure to detect trace-level epichlorohydrin in municipal water systems by HS-SPME-GC/MS

被引:3
作者
Lei, Ping [1 ]
Wang, Lu [1 ]
Yan, Yun [1 ]
Deng, Wubin [1 ]
Gao, Jingsi [2 ]
Zhu, Jia [2 ]
Liang, Miaoqing [2 ]
Wen, Jiaheng [2 ]
Lv, Jianfeng [2 ]
Zhou, Jianfeng [3 ]
机构
[1] Shenzhen Hydrol & Water Qual Ctr, Shenzhen, Guangdong, Peoples R China
[2] Shenzhen Polytech, Shenzhen, Guangdong, Peoples R China
[3] Tianjin Univ GTSI, Georgia Tech Shenzhen Inst, Shenzhen, Guangdong, Peoples R China
来源
FRONTIERS IN CHEMISTRY | 2022年 / 10卷
关键词
epichlorohydrin; headspace solid phase microextraction; sodium sulfate; drinking water systems; gas chromatography mass spectrometry; GAS-CHROMATOGRAPHY; MASS; HEADSPACE; IONS;
D O I
10.3389/fchem.2022.1004269
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Epichlorohydrin (ECH) is toxic to humans via multiple routes and is a potential carcinogen. The accurate measurement of ECH at trace level (< 0.1 mu g/L) is still an obstacle hindering the monitoring and regulation of municipal water systems. In this study, an improved headspace solid-phase microextraction (HS-SPME) procedure is developed and optimized to extract and enrich ECH with high sensitivity, accuracy, and precision. A total 17.4-time enhancement in extraction efficiency is achieved compared with the default condition. Specifically, the AC/PDMS/DVB fiber offered a 4.4-time enhancement comparing with the PDMS/DVB fiber. The effects of different mineral salts in SPME were studied and it was found that an addition of 3 g Na2SO4 in the SPME head achieved an additional 3.3-time increase. The pattern how sodium sulfate enhanced ECH extraction by salting out is discussed. The optimization of extraction conditions (pH = 7, 35 & DEG;C, and 20 min extraction duration) brought another 1.2 times further. Combined with gas chromatography with mass spectrometry, the optimized method exhibits curve linearity in the range of 0.02-1.00 mu g/L with an R-2 of 0.998. The limit of detection, precision, and accuracy of the method are 0.006 mu g/L, 2.6%-5.3%, and -3.5% to -2.0%, respectively. The recovery of ECH spiking in tap water and surface water was investigated, with recovery rates of 88.0%-116% and 72.5%-108%, respectively. Adhering to the requirements of existing water quality regulations, our method shows a high potential to be applied in drinking water quality monitoring and water treatment process assessment.
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页数:8
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