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首页> 外文期刊>Journal of Analytical Atomic Spectrometry >Pulsed radiofrequency glow discharge time of flight mass spectrometry for coated glass analysis
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Pulsed radiofrequency glow discharge time of flight mass spectrometry for coated glass analysis

机译:镀膜玻璃分析的脉冲射频辉光放电飞行时间质谱

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摘要

The analytical potential of radiofrequency pulsed glow discharge time of flight mass spectrometry (rf- PGD-ToFMS) is investigated for quantitative depth profiling analysis of glasses and thin conductive and non-conductive layers on glasses. PGD in combination with ToFMS can allow the reduction or even removal of spectral interferences by selecting a proper GD pulse interval. Thus, discrimination of potential polyatomic interferences for several analytes (e.g., ~(28)Si~+, ~(39)K~+, ~(44)Ca~+, and ~(48)Ti~+) was investigated by selecting appropriate time positions along the GD pulse profile. In this paper, the determination of compositional depth profiles of coated glasses was performed by resorting to a multi-matrix calibration procedure. For this purpose, conductive as well as non-conductive certified reference materials were employed to build the analytical calibration curves. Results show that rf-PGD-ToFMS allows us to discriminate the different layers of the samples and the nominal values for element concentrations and layer thicknesses were in agreement with experimental results obtained using the proposed quantification strategy. Moreover, the capability of rf-PGD-ToFMS to provide a full mass spectrum every 33 μs enable the identification of unexpected elements which can be present as contaminants in very thin layers (e.g. Cd, Sn, Te and Sb).
机译:研究了飞行脉冲质谱仪(rf-PGD-ToFMS)的射频脉冲辉光放电时间的分析潜力,用于对玻璃以及玻璃上的导电薄层和非导电层进行定量深度分析。通过选择适当的GD脉冲间隔,将PGD与ToFMS结合使用可以减少甚至消除频谱干扰。因此,通过选择研究了对几种分析物(例如,〜(28)Si〜+,〜(39)K〜+,〜(44)Ca〜+和〜(48)Ti〜+)的潜在多原子干扰的区分。沿GD脉冲轮廓的适当时间位置。在本文中,通过采用多矩阵校准程序来确定镀膜玻璃的成分深度分布。为此,采用了导电和非导电认证的参考材料来建立分析校准曲线。结果表明,rf-PGD-ToFMS可以区分样品的不同层,元素浓度和层厚度的标称值与使用所提出的定量策略获得的实验结果一致。此外,rf-PGD-ToFMS每33μs提供一次完整质谱的能力使得能够鉴定出意料之外的元素,这些元素可能以污染物形式存在于非常薄的层中(例如Cd,Sn,Te和Sb)。

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  • 来源
    《Journal of Analytical Atomic Spectrometry》 |2015年第5期|1108-1116|共9页
  • 作者单位

    Department of Physical and Analytical Chemistry, Faculty of Chemistry, University of Oviedo, Julian Claveria, 8, 33006 Oviedo, Spain;

    Department of Physical and Analytical Chemistry, Faculty of Chemistry, University of Oviedo, Julian Claveria, 8, 33006 Oviedo, Spain;

    Department of Physics, University of Oviedo, Spain;

    Department of Physical and Analytical Chemistry, Faculty of Chemistry, University of Oviedo, Julian Claveria, 8, 33006 Oviedo, Spain;

    Department of Physical and Analytical Chemistry, Faculty of Chemistry, University of Oviedo, Julian Claveria, 8, 33006 Oviedo, Spain;

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