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Test for arsenic speciation in waters based on a paper-based analytical device with scanometric detection

机译:基于纸张的分析装置的扫描仪检测试验砷形态

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A rapid, simple and affordable method for arsenic speciation analysis is described in this work. The proposed methodology involves in situ arsine generation, transfer of the volatile to the headspace and its reaction with silver nitrate at the detection zone of a paper-based analytical device (PAD). Thus, silver nitrate acts as a recognition element for arsine in the paper-based sensor. The chemical reaction between the recognition element and the analyte derivative results in the formation of a colored product which can be detected by scanning the detection zone and data treatment with an image processing and analysis program. Detection and injection zones were defined in the paper substrate by formation of hydrophobic barriers, thus enabling the formation of the volatile derivative without affecting the chemical stability of the recognition element present in the PAD. Experimental parameters influencing the analytical performance of the methodology, namely color mode detection, composition of the paper-based sensor and hydride generation and mass transfer conditions, were evaluated. Under optimal conditions, the proposed method showed limits of detection and quantification of 1.1 and 3.6 ng mL(-1), respectively. Remarkably, the limit of detection of the method reported herein was much lower than the maximum contaminant levels set by both the World Health Organization and the US Environmental Protection Agency for arsenic in drinking water, unlike several commercially available arsenic test kits. The repeatability, expressed as relative standard deviation, was found to be 7.1% (n = 8). The method was validated against the European Reference Material ERM (R)-CA615 groundwater and successfully applied to the determination of As(III), As(V) and total inorganic As in different water samples. Furthermore, the method can be used for the screening analysis of total arsenic in waters when a cut-off level of 7 ng mL(-1) is used. (C) 2018 Elsevier B.V. All rights reserved.
机译:在这项工作中描述了一种快速,简单,实惠的砷形式分析方法。所提出的方法涉及原位胂生成,将挥发物转移到顶部空间及其与硝酸银在基于纸的分析装置(PAD)的检测区的硝酸银。因此,硝酸银用作纸张传感器中胂的识别元件。识别元件和分析物衍生物之间的化学反应导致形成彩色产品,其可以通过用图像处理和分析程序扫描检测区域和数据处理来检测。通过形成疏水屏障在纸基材中定义检测和注射区域,从而能够形成挥发性衍生物而不影响垫中存在的识别元件的化学稳定性。评估了影响方法的分析性能的实验参数,即颜色模式检测,纸张传感器和氢化物生成的组成和氢化物生成和传质条件。在最佳条件下,所提出的方法分别显示出1.1和3.6ng ml(-1)的检测和定量的限制。值得注意的是,与几种商业上可获得的砷测试试剂盒不同,本文报告的方法的检测限额远低于世界卫生组织和美国环境保护局的最大污染水平。发现作为相对标准偏差的可重复性为7.1%(n = 8)。该方法针对欧洲参考材料ERM(R)-CA615地下水进行验证,并成功地应用于如(iii),如(v)和不同水样中的总无机。此外,当使用7ng ml(-1)的截止水平时,该方法可用于筛选的水中总砷的筛选分析。 (c)2018 Elsevier B.v.保留所有权利。

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