首页> 外文期刊>Journal of Analytical Atomic Spectrometry >Automated headspace single-drop microextraction via a lab-in-syringe platform for mercury electrothermal atomic absorption spectrometric determination after in situ vapor generation
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Automated headspace single-drop microextraction via a lab-in-syringe platform for mercury electrothermal atomic absorption spectrometric determination after in situ vapor generation

机译:在原位蒸气生成后通过实验室平台自动顶空单滴微萃取进行汞电热原子吸收光谱测定

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摘要

A novel fully automated headspace single drop microextraction system based on a programmable lab-in-syringe platform hyphenated to electrothermal atomic absorption spectrometry (ETAAS) for in situ vapor generation assays, was developed. Mixing of precise metered volumes of sample and stannous chloride solutions along with generation of mercury vapor were accomplished inside the microsyringe under reduced pressure environment in a closed manner excluding the possibility of analyte losses. The released of Hg~0 vapor was trapped on the surface of a 25 μL aqueous microdrop consisting of finely dispersed Pd~0 via amalgamation process. Reduced pressure conditions during the preconcentration step increased the extraction rates, resulting in a shorter cycle of analysis and higher sampling frequency. The proposed preconcentration system was fully characterized through optimization of the relevant parameters affecting the generation and sequestration of the vapor of mercury. For 3.5 mL sample, an enhancement factor of 75 was obtained. The detection limit and the precision expressed as relative standard deviation (RSD) were 0.48 μg L~(-1) and 4.2% (at 5.0 μg L~(-1) Hg(Ⅱ) concentration level) respectively. The proposed LIS-SH-SDME-ETAAS method was evaluated by analyzing the IAEA-350 and BCR 278-R certified reference materials as well as environmental water samples.
机译:开发了一种新颖的全自动顶空单滴微萃取系统,该系统基于连接到电热原子吸收光谱法(ETAAS)的可编程注射器实验室平台进行原位蒸汽生成测定。在减压条件下,在微型注射器内部以密闭方式完成了精确计量体积的样品和氯化亚锡溶液的混合以及汞蒸气的产生,排除了分析物损失的可能性。通过汞齐化过程,释放出的Hg〜0蒸气被捕集在由微分散的Pd〜0组成的25μL水微滴的表面上。预浓缩步骤中减压条件的提高提高了萃取率,从而缩短了分析周期并提高了采样频率。通过优化影响汞蒸气产生和隔离的相关参数,对拟议的预浓缩系统进行了全面表征。对于3.5 mL样品,获得的增强因子为75。相对标准偏差(RSD)的检出限和精密度分别为0.48μgL〜(-1)和4.2%(在5.0μgL〜(-1)Hg(Ⅱ)浓度水平下)。通过分析通过IAEA-350和BCR 278-R认证的参考材料以及环境水样品,对提出的LIS-SH-SDME-ETAAS方法进行了评估。

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  • 来源
    《Journal of Analytical Atomic Spectrometry》 |2014年第8期|1491-1498|共8页
  • 作者单位

    Laboratory of Analytical Chemistry, Department of Chemistry, Aristotle University, Thessaloniki 54124, Greece;

    Laboratory of Analytical Chemistry, Department of Chemistry, Aristotle University, Thessaloniki 54124, Greece;

    Laboratory of Analytical Chemistry, Department of Chemistry, Aristotle University, Thessaloniki 54124, Greece;

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