首页> 外文期刊>Talanta: The International Journal of Pure and Applied Analytical Chemistry >Ionic liquid-based miniaturized aqueous biphasic system to develop an environmental-friendly analytical preconcentration method
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Ionic liquid-based miniaturized aqueous biphasic system to develop an environmental-friendly analytical preconcentration method

机译:基于离子液体的小型化水性双相系统,开发一种环保的分析预浓缩方法

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Two ILs containing guanidinium cations (butylguanidinium chloride -C(4)Gu-Cl- and hexylguanidinium chloride -C(6)Gu-Cl-) were synthesized and characterized. Their cytotoxicity was also assessed, obtaining adequate CC50 values of 680 +/- 99 mg.L-1 for C(4)Gu-Cl and 135 +/- 8 mg.L-1 for C(6)Gu-Cl. Miniaturized aqueous biphasic systems (mu-ABSs) were developed using amounts lower than 1% (w/w) of these synthesized guanidinium-based Its, K3PO4 as salting-out agent, and ultrapure water. The phases diagrams of both systems were determined, and the C(4)Gu-Cl-based mu-ABS was selected for the development of a microextraction method in combination with high performance liquid chromatography (HPLC) with fluorescence detection (FD) for the determination of five polycyclic aromatic hydrocarbons (PAHs) as model analytes. A point of the biphasic region of the C(4)Gu-Cl-based mu-ABS corresponding to a mixture of 0.75% (w/w) of the IL, 37.7% (w/w) of K3PO4 and 61.55% (w/w) of ultrapure water, and 30 min of equilibrium time, were selected as optimum conditions to obtain high enrichment factors and proper analytical microextraction performance. The C(4)Gu-Cl-based mu-ABS-HPLC-FD method exhibited low limits of detection, between 0.010 ng.L-1 and 2.0 ng.L-1, average relative recoveries of 96.7%, high enrichment factors ranging from 44.1 to 60.4, average extraction efficiencies of 61.7%, and intermediate precision relative standard deviations lower than 17% for a concentration level of 12 ng.L-1. The developed method was applied successfully in the analysis of different tap water samples.
机译:合成含有胍阳离子(氯胍-C(4)Gu-Cl-和氯化胍-C(6)GU-CL-)的两种ILS。还评估了它们的细胞毒性,得到了C(4)GU-Cl的980 +/- 99mg.L-1和135 +/- 8mg.L-1的足够CC 50值。使用小于1%(w / w)的这些合成的胍基的其基于K3PO4作为盐析药和超纯水来开发小型化的双相系统(MU-ABS)。确定了两个系统的阶段图,并选择C(4)基于C1的MU-ABS,用于开发与高性能液相色谱(HPLC)组合的微萃取方法,具有荧光检测(FD)测定五个多环芳烃(PAHS)作为模型分析物。 C(4)基于C(4)的基于C(4)的u-ang的两种点对应于IL的0.75%(w / w)的混合物,37.7%(w / w)的K3po4和61.55%(w选择超纯水和30分钟的平衡时间,选择最佳条件,以获得高富集因子和适当的分析微萃取性能。基于C(4)的基于GU-CL的MU-ABS-HPLC-FD方法表现出低的检测限,0.010ng.L-1和2.0ng.L-1,平均相对回收率为96.7%,高富集因子测量从44.1至60.4,平均提取效率为61.7%,中间精度相对标准偏差低于12ng.L-1的浓度水平低于17%。在分析不同自来水样品的分析中成功应用了开发方法。

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