Development of a solid-phase microextraction fiber by the chemical binding of graphene oxide on a silver-coated stainless-steel wire with an ionic liquid as the crosslinking agent

被引:15
|
作者
Sun, Min [1 ]
Feng, Juanjuan [1 ]
Bu, Yanan [1 ]
Duan, Huimin [1 ]
Wang, Xiaojiao [1 ]
Luo, Chuannan [1 ]
机构
[1] Univ Jinan, Sch Chem & Chem Engn, Key Lab Chem Sensing & Anal Univ Shandong, Jinan 250022, Peoples R China
基金
中国国家自然科学基金;
关键词
Gas chromatography; Graphene oxide; Ionic liquids; Solid-phase microextraction; Stainless-steel wire; POLYBROMINATED DIPHENYL ETHERS; POLYCYCLIC AROMATIC-HYDROCARBONS; ELECTRON-CAPTURE DETECTION; WALLED CARBON NANOTUBES; WATER SAMPLES; GAS-CHROMATOGRAPHY; AQUEOUS SAMPLES; EXTRACTION; COATINGS; SORBENT;
D O I
10.1002/jssc.201400843
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Graphene oxide was bonded onto a silver-coated stainless-steel wire using an ionic liquid as the crosslinking agent by a layer-by-layer strategy. The novel solid-phase microextraction fiber was characterized by scanning electron microscopy, energy-dispersive X-ray spectroscopy and Raman microscopy. A multilayer graphene oxide layer was closely coated onto the supporting substrate. The thickness of the coating was about 4 mu m. Coupled with gas chromatography, the fiber was evaluated using five polycyclic aromatic hydrocarbons (fluorene, anthracene, fluoranthene, 1,2-benzophenanthrene, and benzo(a) pyrene) as model analytes in direct-immersionmode. Themain conditions (extraction time, extraction temperature, ionic strength, and desorption time) were optimized by a factor-by-factor optimization. The as-established method exhibited a wide linearity range (0.5-200 mu g/L) and low limits of determination (0.05-0.10 mu g/L). It was applied to analyze environmental water samples of rain and river water. Three kinds of the model analytes were quantified and the recoveries of samples spiked at 10 mu g/L were in the range of 92.3-120 and 93.8-115%, respectively. The obtained results indicated the fiber was efficient for solid-phase microextraction analysis.
引用
收藏
页码:3691 / 3698
页数:8
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