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首页> 外文期刊>Analytica chimica acta >Arsenic fractionation in agricultural soil using an automated three-step sequential extraction method coupled to hydride generation-atomic fluorescence spectrometry
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Arsenic fractionation in agricultural soil using an automated three-step sequential extraction method coupled to hydride generation-atomic fluorescence spectrometry

机译:使用自动化的三步连续萃取方法结合氢化物发生原子荧光光谱法对农业土壤中的砷进行分馏

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A fully automated modified three-step BCR flow-through sequential extraction method was developed for the fractionation of the arsenic (As) content from agricultural soil based on a multi-syringe flow injection analysis (MSFIA) system coupled to hydride generation-atomic fluorescence spectrometry (HGAFS). Critical parameters that affect the performance of the automated system were optimized by exploiting a multivariate approach using a Doehlert design. The validation of the flow-based modified-BCR method was carried out by comparison with the conventional BCR method. Thus, the total As content was determined in the following three fractions: fraction 1 (F1), the acid-soluble or interchangeable fraction; fraction 2 (F2), the reducible fraction; and fraction 3 (F3), the oxidizable fraction. The limits of detection (LOD) were 4.0, 3.4, and 23.6 mu g L (1) for F1, F2, and F3, respectively. A wide working concentration range was obtained for the analysis of each fraction, i.e., 0.013-0.800, 0.011-0.900 and 0.079-1.400 mu g L (1) for F1, F2, and F3, respectively. The precision of the automated MSFIA-HG-AFS system, expressed as the relative standard deviation (RSD), was evaluated for a 200 mu g L (1) As standard solution, and RSD values between 5 and 8% were achieved for the three BCR fractions. The new modified three-step BCR flow-based sequential extraction method was satisfactorily applied for arsenic fractionation in real agricultural soil samples from an arsenic-contaminated mining zone to evaluate its extractability. The frequency of analysis of the proposed method was eight times higher than that of the conventional BCR method (6 vs 48 h), and the kinetics of lixiviation were established for each fraction. (C) 2015 Elsevier B.V. All rights reserved.
机译:基于多注射器流动注射分析(MSFIA)系统和氢化物发生-原子荧光光谱法,开发了一种全自动改良的三步BCR流通式顺序萃取方法,用于分离农业土壤中的砷(As)含量(HGAFS)。通过使用Doehlert设计的多变量方法,优化了影响自动化系统性能的关键参数。通过与常规BCR方法进行比较,对基于流程的改进BCR方法进行了验证。因此,总砷含量由以下三个部分确定:部分1(F1),酸可溶或可互换的部分;分数2(F2),可还原分数;和级分3(F3),可氧化级分。 F1,F2和F3的检出限(LOD)分别为4.0、3.4和23.6μg L(1)。对于每个组分的分析,获得了较宽的工作浓度范围,即F1,F2和F3分别为0.013-0.800、0.011-0.900和0.079-1.400μg L(1)。对于200μg L(1)作为标准溶液,评估了自动MSFIA-HG-AFS系统的精度,以相对标准偏差(RSD)表示(3)达到的RSD值在5%至8%之间BCR分数。新的改进的基于三步BCR流动的顺序提取方法已令人满意地应用于来自受砷污染的采矿区的真实农业土壤样品中的砷分馏,以评估其提取能力。所提出方法的分析频率是常规BCR方法的分析频率的八倍(6 vs 48 h),并且为每个级分建立了浸滤动力学。 (C)2015 Elsevier B.V.保留所有权利。

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