首页> 外文期刊>Talanta: The International Journal of Pure and Applied Analytical Chemistry >Electro-enhanced hollow fiber membrane liquid phase microextraction of Cr(VI) oxoanions in drinking water samples
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Electro-enhanced hollow fiber membrane liquid phase microextraction of Cr(VI) oxoanions in drinking water samples

机译:饮用水样品中Cr(VI)含氧阴离子的电增强中空纤维膜液相微萃取

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Hollow fiber membrane liquid phase microextraction (HF-LPME) of metal oxoanions was studied using an ionic carrier enhanced by the application of an electric field (electro-enhanced HF-LPME). The Cr(VI) oxoanion was used as the model. The transportation of Cr(VI) oxoanions across the supported liquid membrane (SLM) was explored via the ion-exchange process and electrokinetic migration. The type of SLM, type of acceptor solution, extraction time, electric potential, and stirring rate were investigated and optimized using MilliQ water. Electra-enhanced HF-LPME provided a much higher enrichment factor compared to conventional HF-LPME (no electric potential) for the same extraction time. A mixture of an anion exchange carrier (methyltrialkyl-ammonium chloride, Aliquat 336) in the SLM facilitated the transportation of Cr(VI) oxoanions. The SLM that gave the best performance was 1-heptanol mixed with 5% Aliquat 336 with 1 M NaOH as the acceptor. Linearity was obtained in the working range of 3-15 mu g L-1 Cr(VI) (R-2 > 0.99) at 30 V with a 5 min extraction time. The limit of detection was below 5 mu g L-1. The relative standard deviation was less than 12%. The method was applied to drinking water samples. The recoveries of spiked Cr(VI) in drinking water samples were in the range of 96-101% based on the matrix-matched calibration curves. The method was limited to samples containing low levels of ions due to the occurrence of electrolysis. The type of SLM, particularly regarding its resistance, should be tuned to control this problematic phenomenon. (C) 2015 Elsevier B.V. All rights reserved.
机译:对金属含氧阴离子的中空纤维膜液相微萃取(HF-LPME)进行了研究,使用了通过施加电场增强的离子载体(电增强HF-LPME)。 Cr(VI)含氧阴离子用作模型。通过离子交换过程和电动迁移,探索了Cr(VI)氧阴离子在载体液膜(SLM)上的运输。使用MilliQ水对SLM的类型,受体溶液的类型,萃取时间,电势和搅拌速率进行了研究和优化。与传统的HF-LPME(无电位)相比,在相同的萃取时间内,电增强的HF-LPME提供了更高的富集因子。 SLM中阴离子交换载体(甲基三烷基氯化铵,Aliquat 336)的混合物促进了Cr(VI)含氧阴离子的运输。提供最佳性能的SLM是1庚醇与5%Aliquat 336的混合液,其中1 M NaOH为受体。在30 V的3-15μgL-1 Cr(VI)(R-2> 0.99)的工作范围内,以5分钟的萃取时间获得了线性。检测限低于5μgL-1。相对标准偏差小于12%。该方法适用于饮用水样品。根据基质匹配的校准曲线,饮用水样品中加标的Cr(VI)的回收率在96-101%的范围内。由于发生电解,该方法仅限于离子含量低的样品。 SLM的类型,尤其是其抵抗力,应调整以控制这种有问题的现象。 (C)2015 Elsevier B.V.保留所有权利。

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