Solid phase microextraction of polycyclic aromatic hydrocarbons by using an etched stainless-steel fiber coated with a covalent organic framework

被引:58
|
作者
Yang, Xiumin [1 ]
Wang, Junmin [1 ]
Wang, Wenjin [1 ]
Zhang, Shuaihua [1 ]
Wang, Chun [1 ]
Zhou, Junhong [2 ]
Wang, Zhi [1 ]
机构
[1] Hebei Agr Univ, Coll Sci, Baoding 071001, Peoples R China
[2] Chinese Acad Sci, Shanghai Inst Organ Chem, Shanghai 200032, Peoples R China
基金
中国国家自然科学基金;
关键词
Density functional theory; Gas chromatography; Mass spectrometry; Response surface methodology; Real water samples; EXTRACTION; CHEMISTRY; RICH;
D O I
10.1007/s00604-019-3258-3
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
A new covalent organic framework (COF) was synthesized by the amide coupling between 1,3,5-tris(4-aminophenyl)benzene and trimesoyl chloride at room temperature. The COF was applied as a steelfiber coating for the solid phase microextraction of polycyclic aromatic hydrocarbons (PAHs) from water samples. The effect of extraction time, salt concentration, and extraction temperature on the efficiency of SPME was optimized by a Box-Behnken design. The PAHs were quantified by gas chromatography with mass spectrometric detection. Figures of merit include (a) a wide linear range (typically from 0.2ngL(-1) to 2gL(-1)), (b) low limits of detection (0.29 to 0.94ngL(-1) at S/N=3), and (c) high enrichment factors (EFs; 819-2420). Density functional theory was employed to study the interaction between the COF cluster and the PAHs. The results demonstrated that the EFs increase with the enhancement of stacking interaction. The repeatability (one fiber; n=5) and reproducibility (fiber to fiber; n=5), expressed as the relative standard deviations were in the range of 4.3%-8.4% and 8.5-11.0%, respectively. The recoveries of the PAHs from water samples spiked at levels of 20.0 and 100ngL(-1) ranged from 79.0% to 105.0%.
引用
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页数:8
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