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首页> 外文期刊>Journal of chromatography, A: Including electrophoresis and other separation methods >Multiple headspace solid-phase microextraction of 2-cyclopentyl-cyclopentanone in polyamide 6.6: possibilities and limitations in the headspace analysis of solid hydrogen-bonding matrices
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Multiple headspace solid-phase microextraction of 2-cyclopentyl-cyclopentanone in polyamide 6.6: possibilities and limitations in the headspace analysis of solid hydrogen-bonding matrices

机译:聚酰胺6.6中2-环戊基-环戊酮的多次顶空固相微萃取:固体氢键合基质顶空分析的可能性和局限性

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The interactions between a polar analyte, 2-cyclopentyl-cyclopentanone, and a solid polar matrix, polyamide 6.6, during multiple headspace solid-phase microextraction (MHS-SPME) were studied. Strong hydrogen bonding between the analyte and the matrix was observed and shown to cause slow migration and adsorption of the analyte. These matrix effects led to erroneous quantitation despite the use of multiple headspace extraction. Addition of water disrupted the hydrogen bonding between the analyte and the matrix and a valid quantitation was achieved. The addition of water also increased the sensitivity and allowed the identification of 2,5-bis(cyclopentyl)-1-cyclopentanone. The amount of 2-cyclopentyl-cyclopentanone in five different polyamide 6.6 samples was measured using the developed multiple headspace solid-phase microextraction method with water-displacer. The measured concentrations were in the range of 1.44-15.61 mug/g. These concentrations were up to 30% higher than the concentrations measured after microwave-assisted extraction (MAE), which indicates incomplete recovery by MAE. The use of water as a displacer eliminated the matrix effects and complete recovery of the analyte was achieved by MHS-SPME. (C) 2004 Elsevier B.V. All rights reserved.
机译:研究了多次顶空固相微萃取(MHS-SPME)过程中极性分析物2-环戊基-环戊酮与固体极性基质聚酰胺6.6的相互作用。观察到分析物与基质之间的强氢键结合,显示出导致分析物缓慢迁移和吸附的原因。尽管使用了多个顶空萃取,但这些基质效应仍导致定量错误。加水破坏了分析物与基质之间的氢键,实现了有效的定量。加水还增加了灵敏度,并允许鉴定2,5-双(环戊基)-1-环戊酮。使用开发的带有水置换器的多顶空固相微萃取方法测量了五个不同的聚酰胺6.6样品中2-环戊基-环戊酮的含量。测得的浓度在1.44-15.61马克杯/克的范围内。这些浓度比微波辅助萃取(MAE)后测得的浓度高30%,这表明MAE回收的不完全。使用水作为置换剂消除了基体效应,并且通过MHS-SPME实现了分析物的完全回收。 (C)2004 Elsevier B.V.保留所有权利。

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