Polydimethylsiloxane/metal-organic frameworks coated stir bar sorptive extraction coupled to gas chromatography-flame photometric detection for the determination of organophosphorus pesticides in environmental water samples

被引:72
|
作者
Xiao, Zuowei [1 ]
He, Man [1 ]
Chen, Beibei [1 ]
Hu, Bin [1 ]
机构
[1] Wuhan Univ, Dept Chem, Key Lab Analyt Chem Biol & Med, Minist Educ, Wuhan 430072, Peoples R China
基金
中国国家自然科学基金;
关键词
MIL-101-Cr-NH2; Stir bar sorptive extraction; Organophosphorus pesticides; Gas chromatography; Environmental waters; SOLID-PHASE MICROEXTRACTION; POLYCYCLIC AROMATIC-HYDROCARBONS; PERFORMANCE LIQUID-CHROMATOGRAPHY; MASS-SPECTROMETRY; POLYCHLORINATED-BIPHENYLS; FIBER; NANOPARTICLES; OPTIMIZATION; FABRICATION; MIL-101;
D O I
10.1016/j.talanta.2016.05.001
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
In this work, the metal-organic frameworks (MOFs), MIL-101-Cr-NH2 was synthesized via a direct hydrothermal method, and a polydimethylsiloxane (PDMS)/MIL-101-Cr-NH2 coated stir bar was prepared by sol-gel technique. Good reproducibility was obtained for the preparation of PDMS/MIL-101-Cr-NH2 coated stir bar with the relative standard deviations (RSDs) ranging from 3.7 to 5.2% (n=7) in one batch, and from 5.4 to 9.2% (n=7) among different batches. With the high surface area and rich benzene ring structure of MIL-101-Cr-NH2, the prepared PDMS/MIL-101-Cr-NH2 coated stir bar presented higher extraction efficiency for target organophosphorus pesticides (OPPs, including phorate, diazinon, malathion, fenthion, quinalphos and ethion) over PDMS coated stir bar. Based on it, a new method of PDMS/MIL-101-Cr-NH2 coated stir bar sorptive extraction (SBSE) coupled to gas chromatography-flame photometric detection (GC-FPD) was proposed for the determination of six OPPs in environmental water samples. The operation parameters affecting the extraction efficiency of SBSE, including extraction time, stirring rate, desorption time and ionic strength, were investigated. Under the optimal conditions, the limits of detection (S/N=3) were found to be in the range of 0.043-0.085 mu g L-1 for the six target OPPs, and the linear range was 0.5-100 mu g L-1 for malathion and 0.2-100 mu g L-1 for other five OPPs. The RSDs of the proposed method evaluated at 1 mu g L-1 for, each OPP were in the range of 5.9-8.7% (intra-day, n=7) and 6.1-10.7% (inter-day, n=5), respectively. The enrichment factors were varied from 110 to 151 fold (theoretical enrichment factor was 200-fold). The proposed method was applied to the analysis of OPPs in East Lake and pond water samples with recoveries in the range of 89.3-115% and 80.0-113% for the spiked East Lake and pond water samples, respectively. (C) 2016 Elsevier B.V. All rights reserved.
引用
收藏
页码:126 / 133
页数:8
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