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首页> 外文期刊>Talanta: The International Journal of Pure and Applied Analytical Chemistry >Optimization of dispersive liquid-liquid microextraction of copper (II) by atomic absorption spectrometry as its oxinate chelate: Application to determination of copper in different water samples
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Optimization of dispersive liquid-liquid microextraction of copper (II) by atomic absorption spectrometry as its oxinate chelate: Application to determination of copper in different water samples

机译:原子吸收光谱法测定含氧螯合剂铜(II)的分散液-液微萃取的优化:在不同水样中测定铜的应用

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摘要

In this study a dispersive liquid-liquid microextraction (DLLME) method based on the dispersion of an extraction solvent into aqueous phase in the presence of a dispersive solvent was investigated for the preconcentration of Cu2+ ions. 8-Hydroxy quinoline was used as a chelating agent prior to extraction. Flame atomic absorption spectrometry using an acetylene-air flame was used for quantitation of the analyte after preconcentration. The effect of various experimental parameters on the extraction was investigated using two optimization methods, one variable at a time and central composite design. The experimental design was performed at five levels of the operating parameters. Nearly the same results for optimization were obtained using both methods: sample size 5 mL; volume of dispersive solvent 1.5 mL; dispersive solvent methanol; extracting solvent chloroform; extracting solvent volume 250 mu L; 8-hydroxy quinoline concentration and salt amount do not affect significantly the extraction. Under the optimum conditions the calibration graph was linear over the range 50-2000 mu g L-1. The relative standard deviation was 5.1% for six repeated determinations at a concentration of 500 mu g L-1. The limit of detection (S/N = 3) was 3 mu g L-1. (C) 2007 Elsevier B.V. All rights reserved.
机译:在这项研究中,研究了基于分散溶剂存在下萃取溶剂向水相中分散的分散液-液微萃取(DLLME)方法对Cu2 +离子的预浓缩。在萃取之前,将8-羟基喹啉用作螯合剂。使用乙炔-空气火焰的火焰原子吸收光谱法用于对预浓缩后的分析物进行定量。使用两种优化方法研究了各种实验参数对提取的影响,其中一种是一次变量,另一种是中央复合设计。实验设计是在五个级别的操作参数上进行的。使用两种方法获得的优化结果几乎相同:样品量5 mL;分散溶剂体积1.5 mL;分散溶剂甲醇;萃取溶剂氯仿;提取溶剂量250μL; 8-羟基喹啉浓度和盐量不会显着影响提取。在最佳条件下,校准曲线在50-2000μg L-1范围内呈线性。在500μg L-1的浓度下进行六次重复测定,相对标准偏差为5.1%。检测限(S / N = 3)为3μg L-1。 (C)2007 Elsevier B.V.保留所有权利。

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