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Silver nanoparticle-assisted preconcentration of selenium and mercury on quartz reflectors for total reflection X-ray fluorescence analysis

机译:石英反射器上银纳米颗粒辅助的硒和汞的预富集,用于全反射X射线荧光分析

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摘要

In this work, a new analytical approach based on the trapping of Se and Hg vapours using silver nanoparticles (Ag NPs) immobilized on quartz reflectors, prior to their determination by total reflection X-ray fluorescence (TXRF), is proposed. Ag NPs were synthesized by reduction of the metal precursor with a reducing agent in aqueous solution. Silanization with 3-mercaptopropyltrimethoxysilane (MPTMS) was used in order to modify the quartz reflectors and immobilize Ag NPs by interaction between the organosilane compound and Ag NPs. A comprehensive characterization of synthesized Ag NPs was carried out by Scanning Electron Microscopy (SEM) and Transmission Electron Microscopy (TEM). SeH_2 and Hg(0) vapours were generated by means of a continuous flow vapour generation system and trapped onto the quartz reflector containing immobilized Ag NPs. Different parameters involved in both the Ag NP synthesis and the continuous flow system for vapour generation and preconcentration were optimized in order to obtain the best results. Detection limits were 0.18 and 0.55 μq L~(-1) for selenium and mercury, respectively. Enrichment factors of 265 and 175 were obtained for Se and Hg, respectively. The new method was successfully validated against three biological certified reference materials and applied to several seafood samples. Recoveries carried out on three certified reference materials were in the range 94-106% with a relative standard deviation of 5% (N = 5).
机译:在这项工作中,提出了一种新的分析方法,该方法基于使用固定在石英反射器上的银纳米颗粒(Ag NPs)捕获硒和汞蒸气,然后通过全反射X射线荧光(TXRF)测定它们。通过在水溶液中用还原剂还原金属前体来合成Ag NP。使用3-巯基丙基三甲氧基硅烷(MPTMS)进行硅烷化是为了修饰石英反射镜并通过有机硅烷化合物和Ag NP之间的相互作用固定Ag NP。通过扫描电子显微镜(SEM)和透射电子显微镜(TEM)对合成的Ag NPs进行了全面表征。 SeH_2和Hg(0)蒸气是通过连续流动的蒸气发生系统产生的,并被捕获到含有固定化Ag NP的石英反射器上。为了获得最佳结果,优化了Ag NP合成和蒸汽产生和预浓缩连续流系统中涉及的不同参数。硒和汞的检出限分别为0.18和0.55μqL〜(-1)。硒和汞的富集因子分别为265和175。该新方法已针对三种生物认证参考材料进行了成功验证,并已应用于多种海鲜样品。对三种认证标准物质的回收率在94-106%范围内,相对标准偏差为5%(N = 5)。

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  • 来源
    《Journal of Analytical Atomic Spectrometry》 |2014年第4期|696-706|共11页
  • 作者单位

    Departamento de Quimica Analitica y Alimentaria, Area de Quimica Analitica, Facultad de Quimica, Universidad de Vigo, Campus As Lagoas-Marcosende s, 36310 Vigo, Spain;

    Departamento de Quimica Analitica y Alimentaria, Area de Quimica Analitica, Facultad de Quimica, Universidad de Vigo, Campus As Lagoas-Marcosende s, 36310 Vigo, Spain;

    Departamento de Quimica Analitica y Alimentaria, Area de Quimica Analitica, Facultad de Quimica, Universidad de Vigo, Campus As Lagoas-Marcosende s, 36310 Vigo, Spain;

    Departamento de Quimica Analitica y Alimentaria, Area de Quimica Analitica, Facultad de Quimica, Universidad de Vigo, Campus As Lagoas-Marcosende s, 36310 Vigo, Spain;

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