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首页> 外文期刊>Journal of Analytical Atomic Spectrometry >A low-blank two-column chromatography separation strategy based on a KMnO_4 oxidizing reagent for Cr isotope determination in micro-silicate samples by thermal ionization mass spectrometry
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A low-blank two-column chromatography separation strategy based on a KMnO_4 oxidizing reagent for Cr isotope determination in micro-silicate samples by thermal ionization mass spectrometry

机译:基于KMnO_4氧化剂的低空白两柱色谱分离策略,通过热电离质谱法测定微硅酸盐样品中的Cr同位素

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摘要

This study has led to a new technique for the separation of Cr from small silicate samples (0.3-2 mg) and determination of stable Cr isotopes in silicates by double spike thermal ionization mass spectrometry (DS-TIMS). Based on our recent two-step exchange resin scheme (Li et al., JAAS, 2016, 31, 2375), we further significantly reduced the procedural blank and improved Cr recovery (94.7-97.5%) from a range of complex silicate rocks varying in composition from andesite to ultra-mafic, and carbonates as well. The key improvement is that KMnO_4 was employed to replace conventional (NH_4)_2S_2O_8 as the oxidizing reagent, which reduces the procedural blank from 1-20 ng in previous studies to 0.15 ± 0.04 ng (n = 8). In addition, the inhibition effect on the Cr signal caused by residual SO_4~(2-) in the Cr fraction using the conventional method has been completely eliminated during TIMS measurements. This permits the high precision determination of Cr isotopic ratios from geological samples as small as ~46 ng. This chemical procedure was verified using a variety of silicate rocks in the size range of 0.3-2 mg. A series of analyses demonstrated that it is possible to attain internal precisions (2 SE) of ±0.03 to 0.06‰. Replicate digestions and analyses of basalt standard BIR-1 with a sample size of 0.3 mg (δ~(53)Cr = -0.158 ± 0.052‰, 2 SD) demonstrated that good intermediate precision is obtainable for extremely small silicate samples.
机译:这项研究导致了一种从小硅酸盐样品(0.3-2 mg)中分离铬并通过双峰热电离质谱法(DS-TIMS)测定硅酸盐中稳定的铬同位素的新技术。基于我们最近的两步交换树脂方案(Li等,JAAS,2016,31,2375),我们进一步减少了一系列复杂硅酸盐岩石中的程序空白并提高了铬的回收率(94.7-97.5%)从安山岩到超镁铁质以及碳酸盐的组成。关键的改进是使用KMnO_4代替了传统的(NH_4)_2S_2O_8作为氧化剂,这将程序空白从以前的研究中的1-20 ng降低到0.15±0.04 ng(n = 8)。此外,在TIMS测量过程中,已经完全消除了使用常规方法由Cr级分中残留SO_4〜(2-)对Cr信号的抑制作用。这样可以从小至46 ng的地质样品中高精度测定Cr同位素比。使用大小范围为0.3-2 mg的各种硅酸盐岩验证了该化学程序。一系列分析表明,有可能获得±0.03至0.06‰的内部精度(2 SE)。样品大小为0.3 mg(δ〜(53)Cr = -0.158±0.052‰,2 SD)的玄武岩标准品BIR-1的重复消化和分析表明,对于极小的硅酸盐样品,可以获得良好的中间精度。

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  • 来源
    《Journal of Analytical Atomic Spectrometry》 |2017年第10期|1938-1945|共8页
  • 作者单位

    State Key Laboratory of Lithospheric Evolution, Institute of Geology and Geophysics, Chinese Academy of Sciences, Beijing 100029, China;

    State Key Laboratory of Lithospheric Evolution, Institute of Geology and Geophysics, Chinese Academy of Sciences, Beijing 100029, China;

    The Institute for Geoscience Research (TIGeR), Department of Applied Geology, Curtin University, GPO Box U1987, Penh, WA6845, Australia,School of Earth Science and Resource, Chang'an University, Xi'an 710054, China;

    The Institute for Geoscience Research (TIGeR), Department of Applied Geology, Curtin University, GPO Box U1987, Penh, WA6845, Australia;

    State Key Laboratory of Lithospheric Evolution, Institute of Geology and Geophysics, Chinese Academy of Sciences, Beijing 100029, China;

    State Key Laboratory of Lithospheric Evolution, Institute of Geology and Geophysics, Chinese Academy of Sciences, Beijing 100029, China;

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