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铁离子诱导增强紫外蒸气发生-原子荧光光谱法测定地表水中超痕量无机砷

Ferric ion induced enhancement of ultraviolet vapour generation coupled with atomic fluorescence spectrometry for the determination of ultratrace inorganic arsenic in surface water.

作者信息

Wang Yuelong, Lin Lingling, Liu Jixin, Mao Xuefei, Wang Jianhua, Qin Deyuan

机构信息

Institute of Quality Standard and Testing Technology for Agro-products, Chinese Academy of Agricultural Sciences, and Key Laboratory of Agro-food Safety and Quality, Ministry of Agriculture, Beijing 100081, China.

Research Center for Analytical Sciences, Northeastern University, Shenyang 110819, China.

出版信息

Analyst. 2016 Feb 21;141(4):1530-6. doi: 10.1039/c5an02489g.

Abstract

A novel method of ultraviolet vapour generation (UVG) coupled with atomic fluorescence spectrometry (AFS) was developed for the determination of ultratrace inorganic arsenic (iAs) in surface water. In this work, different ferric species were utilised for the first time as an enhancement reagent for the ultraviolet vapour generation of As(III), and their UVG efficiencies for volatile species of arsenic were investigated. 15 mg L(-1) of ferric chloride provided the greatest enhancement of approximately 10-fold, using 20% acetic acid combined with 4% formic acid with 30 s ultraviolet irradiation at 200 mL min(-1) Ar/H2 flow rate. Under the optimised conditions, the linear range was 1.0 μg L(-1)-100.0 μg L(-1), and the spiked recoveries were 92%-98%. The limit of detection was 0.05 μg L(-1) for iAs, and the relative standard deviation (RSD) value of the repeated measurements was 2.0% (n = 11). This method was successfully applied to the determination of ultratrace iAs in tap water, river water, and lake water samples using 0.2% H2SO4 (v : v) as the sample preserver. The obtained values for the water samples of certified reference materials (CRMs) including GSB-Z50004-200431, GBW08605 and GBW(E)080390 were all within the certified ranges.

摘要

开发了一种将紫外蒸气发生(UVG)与原子荧光光谱法(AFS)联用的新方法,用于测定地表水中的超痕量无机砷(iAs)。在这项工作中,首次使用不同的铁物种作为砷(III)紫外蒸气发生的增强试剂,并研究了它们对砷挥发性物种的UVG效率。在200 mL min(-1)的Ar/H2流速下,使用20%乙酸与4%甲酸并结合30 s紫外照射,15 mg L(-1)的氯化铁提供了约10倍的最大增强效果。在优化条件下,线性范围为1.0 μg L(-1)-100.0 μg L(-1),加标回收率为92%-98%。iAs的检测限为0.05 μg L(-1),重复测量的相对标准偏差(RSD)值为2.0%(n = 11)。该方法使用0.2% H2SO4(v : v)作为样品保存剂,成功应用于自来水、河水和湖水样品中超痕量iAs的测定。包括GSB-Z50004-200431、GBW08605和GBW(E)080390在内的标准参考物质(CRMs)水样的测定值均在认证范围内。

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