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Gold-Coated Silica as a Preconcentration Phase for the Determination of Total Dissolved Mercury in Natural Waters Using Atomic Fluorescence Spectrometry

机译:原子荧光光谱法测定天然水中总溶解汞的预浓缩相-镀金二氧化硅

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A novel solid-phase preconcentration method is reported, using in-house gold-coated silica adsorbent packed in a microcolumn, for the determination of dissolved mercury in natural waters by atomic fluorescence spectrometry (AFS). The adsorbent was prepared by chemical reduction of a Au(III) solution with hydroxylamine in the presence of suspended silica particles. The resulting Au nanoparticles on the silica surface were highly efficient for adsorbing different mercury species from acidified waters without additional reagents. The acidified aqueous samples were passed over the microcolumn, either incorporated in a fully automated flow injection (FI) system directly coupled to the AFS or as part of a portable FI system for in situ preconcentration. After rinsing and drying of the column, Hg~(0) was released by heating and directed to the AFS cell for quantification. The method offers significant advantages because no reagents are needed for species conversion, preconcentration, sample storage, or desorption and therefore the risk of contamination is minimized and blank values are lowered. This results in a low detection limit of 180 pg L~(-1) using a sample volume of only 7 mL and good reproducibility, with relative standard deviations <3.2percent (n velence 10, [Hg] velence 5 ng L~(-1)). Recoveries were all >90percent in spiked river waters (spiked [Hg] velence 0, 1, 5, 10 ng L~(-1)), and the experimental value for the certified reference material ORMS-4 (elevated mercury in river water) was 22.3 +- 2.6 ng Hg L~(-1) which was in good agreement with the certified value of 22.0 +- 1.6 ng Hg L~(-1) (recovery velence 101percent). The method was successfully applied to seven different natural waters and wastewaters ([Hg] 0.5-4.6 ng L~(-1)) from south west England.
机译:报道了一种新颖的固相预浓缩方法,该方法使用装在微柱中的室内镀金二氧化硅吸附剂,通过原子荧光光谱法(AFS)测定自然水中的溶解汞。通过在悬浮的二氧化硅颗粒存在下用羟胺化学还原Au(III)溶液来制备吸附剂。二氧化硅表面上生成的金纳米粒子无需其他试剂即可高效地从酸化水中吸附不同种类的汞。使酸化的含水样品通过微柱,该微柱可以掺入直接与AFS直接耦合的全自动流动注射(FI)系统中,也可以作为便携式FI系统的一部分进行原位预浓缩。冲洗并干燥色谱柱后,通过加热释放Hg〜(0),并将其导向AFS池进行定量。该方法具有显着的优势,因为不需要试剂进行物质转化,预浓缩,样品存储或解吸,因此污染风险降至最低,空白值降低。使用仅7 mL的样品体积,可实现低检测限180 pg L〜(-1),重现性好,相对标准偏差<3.2%(n velence 10,[Hg] velence 5 ng L〜(- 1))。在加标的河水中(加标浓度为[Hg] velence 0、1、5、10 ng L〜(-1))的回收率均> 90%,经认证的参考物质ORMS-4(河水中的高汞)的实验值为22.3±2.6 ng Hg L〜(-1),与标准值22.0±1.6 ng Hg L〜(-1)吻合良好(回收率101%)。该方法已成功应用于英格兰西南部的7种不同的天然水和废水([Hg] 0.5-4.6 ng L〜(-1))。

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