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Tungsten coil atomic emission spectrometry combined with dispersive liquid–liquid microextraction: A synergistic association for chromium determination in water samples

机译:钨线圈原子发射光谱法与分散液-液微萃取相结合:水样中铬的协同测定

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摘要

A novel and environment friendly analytical method is reported for total chromium determination and chromium speciation in water samples, whereby tungsten coil atomic emission spectrometry (WCAES) is combined with in situ ionic liquid formation dispersive liquid–liquid microextraction (in situ IL-DLLME). A two stage multivariate optimization approach has been developed employing a Plackett–Burman design for screening and selection of the significant factor involved in the in situ IL-DLLME procedure, which was later optimized by means of a circumscribed central composite design. The optimum conditions were complexant concentration: 0.5% (or 0.1%); complexant type: DDTC; IL anion: View the MathML sourcePF6−; [Hmim][Cl] IL amount: 60 mg; ionic strength: 0% NaCl; pH: 5 (or 2); centrifugation time: 10 min; and centrifugation speed: 1000 rpm. Under the optimized experimental conditions the method was evaluated and proper linearity was obtained with a correlation coefficient of 0.991 (5 calibration standards). Limits of detection and quantification for both chromium species were 3 and 10 µg L−1, respectively. This is a 233-fold improvement when compared with chromium determination by WCAES without using preconcentration. The repeatability of the proposed method was evaluated at two different spiking levels (10 and 50 µg L−1) obtaining coefficients of variation of 11.4% and 3.6% (n=3), respectively. A certified reference material (SRM-1643e NIST) was analyzed in order to determine the accuracy of the method for total chromium determination and 112.3% and 2.5 µg L−1 were the recovery (trueness) and standard deviation values, respectively. Tap, bottled mineral and natural mineral water samples were analyzed at 60 µg L−1 spiking level of total Cr content at two Cr(VI)/Cr(III) ratios, and relative recovery values ranged between 88% and 112% showing that the matrix has a negligible effect. To our knowledge, this is the first time that combines in situ IL-DLLME and WCAES.
机译:报道了一种新颖且环保的分析方法,用于测定水中的总铬和铬形态,将钨线圈原子发射光谱法(WCAES)与原位离子液体形成分散液-液微萃取(原位IL-DLLME)结合使用。已经开发了一种采用Plackett-Burman设计的两阶段多元优化方法,用于筛选和选择原位IL-DLLME程序中涉及的重要因素,随后通过外接中央复合设计对其进行了优化。最佳条件是络合剂浓度:0.5%(或0.1%);络合物类型:DDTC; IL阴离子:查看MathML sourcePF6-。 [Hmim] [Cl] IL量:60 mg;离子强度:0%NaCl; pH:5(或2);离心时间:10分钟;离心速度:1000rpm。在优化的实验条件下,对该方法进行了评估,并获得了具有0.991(5个校准标准品)的相关系数的适当线性。两种铬的检出限和定量限分别为3和10 µg L-1。与不使用预浓缩的WCAES测定铬相比,这提高了233倍。在两种不同的加标水平(10和50 µg L-1)下评估了所提出方法的可重复性,分别获得11.4%和3.6%的变异系数(n = 3)。为了确定总铬测定方法的准确性,对经过认证的参考物质(SRM-1643e NIST)进行了分析,回收率(真实度)和标准偏差值分别为112.3%和2.5 µg L-1。在两个Cr(VI)/ Cr(III)比值下,以60 µg L-1的总Cr峰值水平分析自来水,瓶装矿物质和天然矿泉水样品,相对回收率值在88%和112%之间,表明基质的影响可忽略不计。据我们所知,这是首次将原位IL-DLLME和WCAES相结合。

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