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首页> 外文期刊>International journal of environmental analytical chemistry >Determination of methyl mercury in water samples with electromagnetic induction thermal desorption/pyrolysis coupled to atomic fluorescence spectrometry
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Determination of methyl mercury in water samples with electromagnetic induction thermal desorption/pyrolysis coupled to atomic fluorescence spectrometry

机译:电磁感应热解吸/热解-原子荧光光谱法测定水样中的甲基汞

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摘要

A novel non-chromatographic method for the pre-concentration and determination of trace methyl mercury in water samples has been proposed. This method included two main steps: (1) The methyl mercury in sample solution was adsorbed on PDMS of the Fe/SiO2/PDMS bed enrichment column; (2) the analyte was thermally desorbed from the enrichment column and pyrolysed to Hg-0 in an iron particle bed pyrolysis column by using electromagnetic induction heating technique, and then detected by an on-line coupled atomic fluorescence detector. Several factors affecting the enrichment column preparation and concentration procedure have been investigated and optimised. Under optimal condition, the detection limit (3 sigma) was 0.2ngL(-1), along with relative standard deviations of 2.4% (10ngL(-1), N=11) for the repeatability study. The enrichment factor obtained was 108. The two standard reference materials (GBW08675, GBW10029) were analysed to validate the present method. This method was successfully applied to the determination of ngL(-1) methyl mercury in water samples.
机译:提出了一种新型的非色谱方法,用于水样中痕量甲基汞的富集和测定。该方法包括两个主要步骤:(1)将样品溶液中的甲基汞吸附在Fe / SiO2 / PDMS床富集柱的PDMS上; (2)使用电磁感应加热技术,将分析物从富集塔中热解吸,并在铁颗粒床热解塔中热解为Hg-0,然后通过在线耦合原子荧光检测器进行检测。已经研究和优化了影响浓缩柱制备和浓缩程序的几个因素。在最佳条件下,可重复性研究的检出限(3 sigma)为0.2ngL(-1),相对标准偏差为2.4%(10ngL(-1),N = 11)。获得的富集系数为108。分析了两种标准参考物质(GBW08675,GBW10029)以验证本方法。该方法已成功应用于水样中ngL(-1)甲基汞的测定。

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