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首页> 外文期刊>Journal of Analytical Atomic Spectrometry >A novel purification method for high precision measurement of Ni isotopes by double spike MC-ICP-MS
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A novel purification method for high precision measurement of Ni isotopes by double spike MC-ICP-MS

机译:双峰MC-ICP-MS纯化镍同位素的高精度纯化新方法

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摘要

Nickel (Ni) isotopes have been developed as a potential biosignature and proxy for tracing the occurrence of the Great Oxidation Event. However, the precise measurement of Ni isotopes is still hindered by the costly operation, complicated procedures and/or high procedural blanks of the chemical purification schemes. Here, a novel purification scheme, utilizing only dimethylglyoxime (DMG) and acetone as organic reagents, is proposed to separate Ni from samples through a four-step procedure with five chromatographic columns. Steps I, II and III are designed to effectively eliminate major matrix elements, including 99% Fe, Ca, Ti, and Al, 85% Mn, 55% K, even for samples with [Ca]/[Ni] approximate to 4600 and [Mg]/[Ni] approximate to 1900. Step IV utilizes the formation of Ni(DMG)(2) complexes in an aqueous medium containing 0.5 M HCl, 95% acetone and 0.1 M DMG, which can remove residual elements such as 45% K; this step avoids the use of Ni-specific resin, which requires careful pH tuning. Steps III and I can be repeated to obtain high-purity Ni. The Ni yield through these four steps is greater than 92%, with a maximum loss of similar to 8% occurring in Step II for low-Ni samples. The total procedural blank is 0.4 to 1.2 ng. When double spiking (Ni-61-Ni-60) is used to correct for instrument mass bias and purification-related isotope fractionation, small sample sizes (600-800 ng) are sufficient for achieving high-precision Ni isotope determination. Nickel isotopes for standards such as SRM 986 and geological reference materials (GRMs) such as BHVO-2, NOD-P-1, and NOD-A were determined on a Nu Plasma III MC-ICP-MS. The long-term reproducibility is 0.05 parts per thousand (2SD, n = 134) for pure solution and 0.06 parts per thousand (2SD, n = 18) for GRMs, and the average delta Ni-60 values are in excellent agreement with previous studies. These results show that our new purification method can be applied to various samples. Using this new method, we measured a set of granite, sediment, diamictite and loess samples and preliminarily constrained the delta Ni-60 of the upper continental crust to be 0.11 +/- 0.14 parts per thousand (2SD, n = 17).
机译:镍(Ni)同位素已被开发为潜在的生物特征和跟踪大氧化事件发生的替代物。然而,镍同位素的精确测量仍然受到昂贵的操作,复杂的程序和/或化学纯化方案的高程序空白的阻碍。在此,提出了一种仅使用二甲基乙二肟(DMG)和丙酮作为有机试剂的新型纯化方案,该方法通过具有五个色谱柱的四步过程从样品中分离出Ni。步骤I,II和III旨在有效消除主要基质元素,包括99%Fe,Ca,Ti和Al,85%Mn,55%K的元素,即使对于[Ca] / [Ni]约为4600和[Mg] / [Ni]大约为1900。步骤IV利用Ni(DMG)(2)络合物在含有0.5 M HCl,95%丙酮和0.1 M DMG的水性介质中的形成,该介质可以除去残留的元素,例如45 %K;此步骤避免了使用需要对pH进行仔细调节的Ni专用树脂。可以重复步骤III和I,以获得高纯度Ni。通过这四个步骤的镍产率大于92%,对于低镍样品,在步骤II中发生的最大损失接近8%。整个程序空白为0.4到1.2 ng。当使用两次加标(Ni-61-Ni-60)校正仪器的质量偏差和与纯化有关的同位素分馏时,小样本量(600-800 ng)足以实现高精度的Ni同位素测定。在Nu Plasma III MC-ICP-MS上测定了诸如SRM 986等标准品的镍同位素和诸如BHVO-2,NOD-P-1和NOD-A等地质参考物质(GRM)。纯溶液的长期重现性为0.05千分之(2SD,n = 134),GRMs为0.06千分之二(2SD,n = 18),平均Ni-60平均值与先前的研究非常吻合。这些结果表明我们的新纯化方法可应用于各种样品。使用这种新方法,我们测量了一组花岗岩,沉积物,铁矾土和黄土样品,并初步将上大陆壳的δNi-60约束为千分之0.11 +/- 0.14(2SD,n = 17)。

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  • 来源
    《Journal of Analytical Atomic Spectrometry 》 |2019年第8期| 1639-1651| 共13页
  • 作者单位

    China Univ Geosci Beijing, State Key Lab Geol Proc & Mineral Resources, Beijing 100083, Peoples R China;

    China Univ Geosci Beijing, State Key Lab Geol Proc & Mineral Resources, Beijing 100083, Peoples R China;

    Univ S Alabama, Dept Marine Sci, Mobile, AL 36688 USA|Dauphin Isl Sea Lab, Dauphin Isl, AL 36528 USA;

    China Univ Geosci Beijing, State Key Lab Geol Proc & Mineral Resources, Beijing 100083, Peoples R China;

    Chinese Acad Sci, Inst Geochem, State Key Lab Environm Geochem, Guiyang 550081, Guizhou, Peoples R China;

    China Univ Geosci Beijing, State Key Lab Geol Proc & Mineral Resources, Beijing 100083, Peoples R China;

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