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首页> 外文期刊>The Analyst: The Analytical Journal of the Royal Society of Chemistry: A Monthly International Publication Dealing with All Branches of Analytical Chemistry >Development of a new and environment friendly hollow fiber-supported liquid phase microextraction using vesicular aggregate-based supramolecular solvent
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Development of a new and environment friendly hollow fiber-supported liquid phase microextraction using vesicular aggregate-based supramolecular solvent

机译:使用囊泡聚集体型超分子溶剂开发新型环保型中空纤维支持的液相微萃取

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摘要

Hollow fiber-based liquid phase microextraction (HF-LPME) using conventional solvents is limited by their relative instability and high volatility. The use of supramolecular solvents as a liquid membrane phase could overcome these inconveniences due to their negligible vapour pressure and high viscosity. In the present study, a novel and highly flexible method was developed based on supramolecular solvents constructed of vesicles of decanoic acid, which were used for the first time as a solvent in HF-LPME. This solvent is produced from the coacervation of decanoic acid aqueous vesicles by the action of tetrabutylammonium (Bu _4N ~+). In this work, halogenated anilines as model compounds were extracted from water samples into a supramolecular solvent impregnated in the pores and also filled inside the porous polypropylene hollow fiber membrane. The extracted anilines were separated and determined by high-performance liquid chromatography. The technique requires minimal sample preparation time and toxic organic solvent consumption, and provides a significant advantage over conventional analytical methods. The important parameters influencing the extraction efficiency were studied and optimized utilizing two different optimization methods: one variable at a time and the Box-Behnken design. Under the optimum conditions, the preconcentration factors were in the range of 74 to 203. Linearity of the method was obtained in the range of 1.0-100 μg L ~(-1) with the correlation coefficients of determination (R ~2) ranging from 0.9901 to 0.9986. The limits of detection for the target anilines were 0.5-1.0 μg L ~(-1). The relative standard deviations varied from 3.9% to 6.0%. The relative recoveries of the three halogenated anilines from water samples at a spiking level of 20.0 μg L ~(-1) were in the range of 90.4-107.4%.
机译:使用常规溶剂的中空纤维基液相微萃取(HF-LPME)受其相对不稳定和高挥发性的限制。由于超分子溶剂的蒸气压可忽略不计且粘度高,因此使用超分子溶剂作为液膜相可以克服这些不便之处。在本研究中,基于由癸酸囊泡构成的超分子溶剂,开发了一种新颖且高度灵活的方法,该方法首次在HF-LPME中用作溶剂。该溶剂是由癸酸水溶液囊泡在四丁基铵(Bu _4N〜+)作用下凝聚而产生的。在这项工作中,从水样中将卤代苯胺作为模型化合物从浸入孔中的超分子溶剂中提取,并填充在多孔聚丙烯中空纤维膜的内部。分离提取的苯胺并通过高效液相色谱法测定。该技术需要最少的样品制备时间和有毒的有机溶剂消耗,并且比常规分析方法具有明显的优势。使用两种不同的优化方法研究和优化了影响萃取效率的重要参数:一次变量和Box-Behnken设计。在最佳条件下,预富集因子在74至203范围内。方法的线性在1.0至100μgL〜(-1)范围内,测定的相关系数(R〜2)为0.9901至0.9986。目标苯胺的检出限为0.5-1.0μgL〜(-1)。相对标准偏差从3.9%到6.0%不等。尖峰浓度为20.0μgL〜(-1)时,水样品中三种卤代苯胺的相对回收率在90.4-107.4%的范围内。

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