Determination of yttrium in phosphorus powder from fluorescent lamps by microwave-induced optical emission spectrometry (MIP OES) after ultrasound-assisted extraction

IF 2.7 3区 化学 Q2 CHEMISTRY, ANALYTICAL
Glaucia Gisele M. Machado, Graziela S. Silva, Pamela S. M. Rocha, André S. Araújo, Eduardo da S. G. de Castro and Ricardo J. Cassella
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Abstract

In this work, we propose a novel method for yttrium determination by microwave-induced optical emission spectrometry (MIP OES). It is based on the ultrasound-assisted extraction of yttrium with a diluted HNO3 solution and was applied to yttrium determination in phosphorus powder from fluorescent lamps. The method was optimized employing a multivariate strategy, based on a Box–Behnken design, taking into account three experimental factors: mass of the sample (25 to 75 mg), sonication time (15 to 165 min) and HNO3 concentration in the extractant solution (2.0 to 6.0 mol L−1). According to the data obtained in the optimization process, only the sonication time and the HNO3 concentration had an influence on the extraction of yttrium from the samples. The data also indicated that yttrium must be strongly linked to the matrix, since its quantitative extraction was only possible when using the maximum values of the two factors. Therefore, under optimized conditions, we could quantitatively extract yttrium from 75 mg of sample using a 6 mol per L HNO3 solution and a sonication time of 165 min. The limits of detection and quantification for the method were 0.4 and 1.2 μg g−1, respectively, and the intermediary precision (three days) was 14%. The concentration of Y in the analyzed samples varied from 5.37 ± 1.82 to 298 ± 31 μg g−1, and recoveries of 91.0 ± 34.6 and 106 ± 23% were obtained in comparison to total digestion. The results obtained by the proposed method were not statistically different (at the 95% confidence level) from those obtained after the total digestion of the samples when applying the Student's t-test.

Abstract Image

超声辅助萃取后利用微波诱导光学发射光谱法 (MIP OES) 测定荧光灯磷粉中的钇含量
在这项工作中,我们提出了一种利用微波诱导光学发射光谱法(MIP OES)测定钇含量的新方法。该方法以稀释的 HNO3 溶液超声辅助萃取钇为基础,应用于荧光灯磷粉中钇的测定。该方法采用方框-贝肯设计(Box-Behnken design)的多元策略进行优化,考虑了三个实验因素:样品质量(25 至 75 毫克)、超声时间(15 至 165 分钟)和萃取剂溶液中的 HNO3 浓度(2.0 至 6.0 摩尔/升)。根据优化过程中获得的数据,只有超声时间和 HNO3 浓度对样品中钇的萃取有影响。数据还表明,钇必须与基质密切相关,因为只有在使用这两个因子的最大值时,才能对钇进行定量萃取。因此,在优化条件下,使用 6 mol L-1 HNO3 溶液和 165 分钟的超声时间,我们可以从 75 毫克样品中定量提取钇。该方法的检出限和定量限分别为 0.4 和 1.2 µg g-1,中间精度(三天)为 14%。分析样品中 Y 的浓度范围为 5.37± 1.82 至 298 ± 31 µg g-1,与全消解法相比,回收率分别为 91.0 ± 34.6 和 106 ± 23%。通过学生 t 检验,拟议方法得出的结果与样品完全消解后得出的结果没有统计学差异(置信度为 95%)。
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来源期刊
Analytical Methods
Analytical Methods CHEMISTRY, ANALYTICAL-FOOD SCIENCE & TECHNOLOGY
CiteScore
5.10
自引率
3.20%
发文量
569
审稿时长
1.8 months
期刊介绍: Early applied demonstrations of new analytical methods with clear societal impact
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