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Development of a solid-phase microextraction fiber by chemical binding of polymeric ionic liquid on a silica coated stainless steel wire

机译:通过聚合物离子液体在涂有二氧化硅的不锈钢丝上的化学结合来开发固相微萃取纤维

摘要

A novel approach was developed for the fabrication of solid-phase microextraction (SPME) fiber by coating stainless steel fiber with a polymeric ionic liquid (PIL) through covalent bond. The stainless steel fiber was sequentially coated with a gold film by replacement reaction between Fe and Au when immerged in chloroauric acid, assembled with a monolayer of 3-(mercaptopropyl) triethoxysilane on the gold layer through the Au-S bond, and coated with a silica layer by the hydrolysis and polycondensation reaction of the surface-bonded siloxane moieties and the active silicate solution. Then, 1-vinyl-3-(3-triethoxysilylpropyl)-4,5-dihydroimidazolium chloride ionic liquid was anchored on the silica layer by covalent bond, and the PIL film was further formed by free radical copolymerization between 1-vinyl-3-(3-triethoxysilylpropyl)-4,5-dihydroimidazdium and vinyl-substituted imidazolium with azobisisobutyronitrile (AIBN) as initiator. Parameters influencing the preparation of PIL fiber were optimized, and the developed SPME fiber has a coating thickness of similar to 20 mu m with good thermal stability and long lifetime. The performance of the PIL fiber was evaluated by analysis of polycyclic aromatic hydrocarbons (PAHs) in water samples. The developed PIL fiber showed good linearity between 0.5 and 20 mu g l(-1) with regression coefficient in the range of 0.963-0.999, detection limit ranging from 0.05 to 0.25 mu g l(-1), and relative standard deviation of 9.2-29% (n = 7). This developed PIL fiber exhibited comparable analytical performance to commercial 7 p,m thickness PDMS fiber in the extraction of PAHs. The spiked recoveries for three real water samples at 0.5-5 mu g l(-1) levels were 49.6-111% for the PIL fiber and 40.8-103% for the commercial PDMS fiber. (C) 2012 Elsevier B.V. All rights reserved.
机译:通过共价键将聚合物离子液体(PIL)涂覆在不锈钢纤维上,开发了一种用于固相微萃取(SPME)纤维制造的新方法。当浸入氯金酸时,通过Fe和Au之间的置换反应在不锈钢纤维上依次涂上金膜,然后通过Au-S键在金层上用3-(巯基丙基)三乙氧基硅烷单层组装,并用二氧化硅层通过表面键合的硅氧烷部分和活性硅酸盐溶液的水解和缩聚反应而形成。然后,通过共价键将1-乙烯基-3-(3-三乙氧基甲硅烷基丙基)-4,5-二氢咪唑鎓氯化物离子液体锚定在二氧化硅层上,并且通过1-乙烯基-3-之间的自由基共聚进一步形成PIL膜。 (3-三乙氧基甲硅烷基丙基)-4,5-二氢咪唑鎓和乙烯基取代的咪唑鎓,偶氮二异丁腈(AIBN)作为引发剂。优化了影响PIL纤维制备的参数,开发的SPME纤维的涂层厚度接近20μm,具有良好的热稳定性和长寿命。通过分析水样品中的多环芳烃(PAHs)来评估PIL纤维的性能。研制的PIL纤维在0.5和20 mu gl(-1)之间表现出良好的线性,回归系数在0.963-0.999范围内,检出限在0.05-0.25 mu gl(-1)之间,相对标准偏差为9.2-29 %(n = 7)。这种开发的PIL纤维在PAH的萃取中表现出与商用7微米厚的PDMS纤维相当的分析性能。以PIL纤维为0.5-5μg l(-1)的三个真实水样的加标回收率为49.6-111%,商业PDMS纤维为40.8-103%。 (C)2012 Elsevier B.V.保留所有权利。

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    Pang Long; Liu Jing-Fu;

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