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首页> 外文期刊>Analytica chimica acta >Assessing the internal standardization of the direct multi-element determination in beer samples through microwave-induced plasma optical emission spectrometry
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Assessing the internal standardization of the direct multi-element determination in beer samples through microwave-induced plasma optical emission spectrometry

机译:通过微波诱导的等离子体光发射光谱法评估啤酒样品中直接多元素测定的内部标准化

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An evaluation of different elements (Be, Ga, In, Sc, and Y) as internal standards was performed to determine the content of Al, Ba, Co, Cr, Cu, Fe, Mn, Ni, Sr, Zn, Ca, Mg, Na, K in beer samples through microwave induced plasma optical emission spectrometry. The analytes were determined after simple dilutions of the samples with a 1.0 M nitric acid solution at a 1:4 ratio (sample: acid solution) with the addition of the IS. The analytical performance for each potential IS was established based on the limit of detection, limit of quantification, addition and recovery tests and accuracy obtained in the determination of each analyte. Each analyte responded differently when internal standardization was applied, and as such, the evaluation of each IS is important in the development of the method. In the presence of the recommended internal standard, the limit of detection varied, in mu g L-1, from 0.23 to 4.6 for the microelements and between 10 and 620 for the macroelements. The limit of quantification, in mu g L-1, was between 0.78 and 15.4 and between 30 and 970 for the microelements and macroelements, respectively. The precisions of the measurements, expressed as the relative standard deviation (n = 10; 0.50 and 3.0 mg L-1 of each analyte), were lower than 1.0% for all analytes. The proposed method was applied for the multi-element determination in commercial beer samples and the results were compared with those obtained by inductively coupled plasma optical emission spectrometry after sample digestion. (C) 2019 Elsevier B.V. All rights reserved.
机译:进行作为内部标准的不同元素(如,GA,IN,SC和Y)以确定Al,Ba,Co,Cr,Cu,Fe,Mn,Ni,Sr,Zn,Ca,Mg的含量,Na,K通过微波诱导等离子体光发射光谱法在啤酒样品中。通过添加为1:4的比例(样品:酸溶液)的1.0μm硝酸溶液简单地稀释样品后测定分析物。基于检测极限,定量限制,添加和恢复试验和测定中的测定中获得的准确度来建立每个电位的分析性能。当应用内部标准化时,每个分析物的响应不同,因此,每个分析性的评估在该方法的发展中是重要的。在推荐的内标存在下,检测极限在MU G L-1中变化,为微量元件的0.23至4.6和宏观测量的10和620。在MU G L-1中定量的极限分别为0.78和15.4和30至970之间,微量元素和宏观测量。测量的精确性表示为相对标准偏差(每个分析物的N = 10; 0.50和3.0mg L-1),对所有分析物的1.0%低于1.0%。施加的方法用于商业啤酒样品中的多元素测定,并将结果与​​样品消化后通过电感耦合等离子体光发射光谱法获得的结果进行比较。 (c)2019年Elsevier B.V.保留所有权利。

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