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Determination of ultra-trace sulfur in high-purity metals by isotope dilution inductively coupled plasma sector field mass spectrometry combined with chemical separation procedure

机译:同位素稀释电感耦合等离子体扇区质谱法与化学分离过程相结合的高纯度金属中超痕量硫的测定

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摘要

The analytical method of ultra-trace sulfur (S) in high-purity metal by isotope dilution inductively coupled plasma mass spectrometry (ID-ICP-MS) combined with chemical separation procedure was developed in the present study. In order to determine the ultra-trace S in high-purity metal, a chemical separation with alumina column was carried out before ICP-MS measurement. This method enabled to prevent the polyatomic ion interference arising from the metal matrix and the signal suppression derived from the space charge effect in ICP-MS. In order to achieve high sensitive analysis, an ICP-sector field mass spectrometer (ICP-SFMS) was used. The isolation of polyatomic ion interference with respect to S was also carried out in medium-resolution mode. In addition, measurement conditions including detector dead time, which affects the precision and accuracy of the isotope dilution method, and washout conditions that were employed to reduce memory effects were optimized. The developed method was validated by the determination of S in a high-purity iron reference material (JSS-001-4). The analytical result obtained by the developed method (1.86 mg kg(-1) +/- 0.12 mg kg(-1) (k = 2)) was in good agreement with the certified value (1.90 mg kg(-1) +/- 0.42 mg kg(-1)). The method was also applied to the determination of S in high-purity zinc, revealing a content of 0.08 mg kg(-1) +/- 0.08 mg kg(-1) (k = 2). Since the developed method enabled the determination of ultra-trace S at pig kg(-1) level in the high-purity zinc, it is expected to be useful for high sensitive and accurate determination of ultra-trace S in high-purity metals.
机译:通过同位素稀释电感耦合等离子体质谱法(ID-ICP-MS)与化学分离程序相结合的高纯度金属中的超痕量硫(S)的分析方法是在本研究中进行的。为了确定高纯度金属中的超痕量S,在ICP-MS测量之前进行与氧化铝塔的化学分离。该方法使能防止由金属矩阵产生的多原子离子干扰和ICP-MS中的空间电荷效应所产生的信号抑制。为了实现高敏感性分析,使用ICP扇形场质谱仪(ICP-SFMS)。还在中分辨率模式下进行多种子离子干扰的分离。此外,包括检测器死区时间的测量条件,这影响了同位素稀释方法的精度和准确性,并优化了用于降低记忆效应的冲洗条件。通过在高纯铁参考物质(JSS-001-4)中的测定验证了开发的方法。通过开发方法获得的分析结果(1.86mg kg(-1)+/- 0.12mg kg(-1)(k = 2))与认证值吻合良好(1.90 mg kg(-1)+ / - 0.42 mg kg(-1))。该方法还应用于高纯度锌中S的测定,揭示含量为0.08mg kg(-1)+/- 0.08mg kg(-1)(k = 2)。由于开发方法使得在高纯度锌中的猪kg(-1)水平中的超痕量S测定,预计将可用于高纯度金属中的超痕量型的高敏感和精确测定。

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