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首页> 外文期刊>Atomic Spectroscopy >Use of Chemometric Tools for HG-AAS Instrumental Optimization in the Determination of Se in Nuts Grown in Brazil
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Use of Chemometric Tools for HG-AAS Instrumental Optimization in the Determination of Se in Nuts Grown in Brazil

机译:化学计量工具对HG-AAS乐器优化的使用,在巴西种植的螺母中的纯化中的优化

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摘要

The determination of total selenium (Se) is described in nuts such as bacuri (Platonia insignis Mart.), baru (Dipteryx alata Vog.), bocaiuva (Acrocomia aculeata (Jacq.) Lodd), and cashew (Anacardium occidentale L.) (other than the well-known Brazilian nut) using hydride generation coupled to a flame atomic absorption spectrometer (HG-AAS). The best experimental conditions to generate the volatile hydride (H2Se) were established by multivariate statistical analysis. The conditions of the pre-reduction step to generate the Se hydride were optimized using the Pareto diagram and Doehlert design. Best results were achieved when 0.6 mol L-1 HCl, 1.0% (m/v) NaBH4 in 0.5% (m/v) NaOH, and a 00-cm reaction coil were used. For Se determination by HG-AAS, analytical curves were built in the 0.50 - 25.0 mu g L-1 range resulting in a linear coefficient correlation better than 0.9970. The accuracy of the sample preparation procedure and HG-AAS determination were evaluated by addition and recovery tests, and the recoveries were found in the 90.3-95.8% range with a relative standard deviation (%RSD) of <4.7%. Using the proposed methodology, the limit of detection obtained was 0.1315 mu g L-1 with a %RSD up to 1.9%. The Se concentrations in the samples were in the 0.515 +/- 0.017-0.657 +/- 0.029 mu g g(-1) Se range. The multivariate analysis applied to the experimental results showed to be a useful tool because it allows reducing the number of experiments (from 60 to 8) with satisfactory accuracy.
机译:全硒(SE)的测定是用BACURI(PLATONIA INSIGNIS MART。),BARU(DIPTERYX ALATA VOG。),BOCAIUVA(acrocomia Aculeata(JACQ)LODD)等螺母中描述,以及腰果(AnaCardium Occidentale L.)(除了众所周知的巴西螺母外,使用氢化物​​产生耦合到火焰原子吸收光谱仪(HG-AAS)。通过多变量统计分析建立产生挥发性氢化物(H2SE)的最佳实验条件。使用帕累托图和道光泽设计优化了产生SE氢化物的预还原步骤的条件。使用0.6mol L-1 HCl,1.0%(M / V)NaOH,1.0%(M / V)NaOH和00-CM反应线圈,实现了最佳结果。对于HG-AAS的SE测定,构建在0.50-25.0μg的分析曲线范围内,导致线性系数相关性优于0.9970。通过加法和回收试验评估样品制备方法和HG-AAS测定的准确性,并在90.3-95.8%范围内发现回收率,相对标准偏差(%RSD)为<4.7%。使用所提出的方法,得到的检测极限为0.1315μgl-1,%RSD高达1.9%。样品中的Se浓度为0.515 +/- 0.017-0.657 +/- 0.029 mu G(-1)SE范围。应用于实验结果的多变量分析显示是一种有用的工具,因为它允许以满意的精度降低实验数量(从60〜8)。

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