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首页> 外文期刊>Journal of Analytical Atomic Spectrometry >On-line speciation of inorganic arsenic in natural waters using polyaniline (PANI) with determination by flow injection-hydride generation-inductively coupled plasma mass spectrometry at ultra-trace levels
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On-line speciation of inorganic arsenic in natural waters using polyaniline (PANI) with determination by flow injection-hydride generation-inductively coupled plasma mass spectrometry at ultra-trace levels

机译:使用聚苯胺(PANI)在线分析天然水中的无机砷,并通过流动注射氢化物发生-电感耦合等离子体质谱法测定超痕量水平

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摘要

A home made PTFE micro-column loaded with polyaniline (50mg), prepared freshly by a chemical method was used for the on-line separation of arsenite [As(Ⅲ)] and arsenate [As(Ⅴ)] followed by determination at ultra trace levels in natural waters by flow injection-hydride generation-inductively coupled plasma mass spectrometry (FI-HG-ICPMS). The species were determined using time resolved mode of data acquisition, by monitoring ~(75)As. The volume of sample injected was 100μl. Both the species eluted within 3min. The effects of variation in sample pH, eluent concentration and the hydride generation conditions were investigated. The calibration in the range of 0.5-50μg L~(-1) was found to be linear with a regression coefficient, R~2 ≥ 0.997. The detection limits (3σ) were calculated to be 0.05 and 0.09μg L~(-1) for As(Ⅲ) and As(Ⅴ) respectively and the precision (%RSD) at 1μg L~(-1) level was found to be 2.0% for As(Ⅲ) and 2.5% As(Ⅴ). The method validation was carried out by analyzing two BCR groundwater certified reference materials, BCR609 and BCR610, certified for total arsenic. The developed speciation method has been applied to groundwater samples collected from West Bengal, India, where there have been many instances of arsenic contamination.
机译:化学方法新鲜制备的载有聚苯胺(50mg)的自制PTFE微柱用于在线分离亚砷酸盐[As(Ⅲ)]和砷酸盐[As(Ⅴ)],然后超痕量测定流动注射氢化物发生-电感耦合等离子体质谱法(FI-HG-ICPMS)测定天然水中的三价。通过监测〜(75)As,使用时间分辨数据采集模式确定物种。进样量为100μl。两种物种均在3分钟内洗脱。研究了样品pH,洗脱液浓度和氢化物生成条件变化的影响。在0.5〜50μgL〜(-1)范围内校正为线性,回归系数为R〜2≥0.997。计算出As(Ⅲ)和As(Ⅴ)的检出限(3σ)分别为0.05和0.09μgL〜(-1),发现在1μgL〜(-1)浓度下的精密度(%RSD)为砷(Ⅲ)为2.0%,砷(Ⅴ)为2.5%。通过对两种BCR地下水认证参考物质BCR609和BCR610进行总砷认证,对方法进行了验证。发达的物种形成方法已应用于从印度西孟加拉邦收集的地下水样本,那里有许多砷污染的实例。

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  • 来源
    《Journal of Analytical Atomic Spectrometry》 |2010年第8期|P.1348-1353|共6页
  • 作者单位

    National Centre for Compositional Characterization of Materials (C.C.C.M.), Bhabha Atomic Research Centre, D.A.E.,ECIL Post, Hyderabad, 500062, India;

    National Centre for Compositional Characterization of Materials (C.C.C.M.), Bhabha Atomic Research Centre, D.A.E.,ECIL Post, Hyderabad, 500062, India;

    National Centre for Compositional Characterization of Materials (C.C.C.M.), Bhabha Atomic Research Centre, D.A.E.,ECIL Post, Hyderabad, 500062, India;

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