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首页> 外文期刊>Journal of Analytical Atomic Spectrometry >Multi-element ion-exchange chromatography and high-precision MC-ICP-MS isotope analysis of Mg and Ti from sub-mm-sized meteorite inclusions
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Multi-element ion-exchange chromatography and high-precision MC-ICP-MS isotope analysis of Mg and Ti from sub-mm-sized meteorite inclusions

机译:亚毫米大小陨石包裹体中Mg和Ti的多元素离子交换色谱法和高精度MC-ICP-MS同位素分析

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摘要

The analytical improvement of new generation mass spectrometers has reached a level required for high-precision isotope analysis of very small and unique natural samples. The multi-element isotopic signatures of meteorite inclusions can potentially provide detailed insight into the origin of our solar system. As such, in-line separation and isotope analysis of multiple elements from such unique samples is highly desirable, but rarely accommodated by current chromatographic purification procedures necessary for accurate isotope analysis using multiple collector inductively coupled plasma source mass spectrometry (MC-ICP-MS). Here, we report a new multi-element ion chromatographic purification procedure, specifically developed for the separation of very small amounts of Mg (~5 μg) and Ti (0.7-1 ng) from individual samples. Highly isotopically anomalous sub-mm sized materials, such as Ca-AI-rich inclusions in primitive meteorites, can be routinely analysed for their mass-independent μ(~26)Mg~*, μ~(45)Ti~*,μ~(48)Ti~*, μ~(49)Ti~* and μ~(50)Ti~* isotope compositions with an estimated external reproducibility of 4.1, 11, 8.8, 18 and 12 ppm (2sd), respectively. These procedures consume significantly less material than previous methods and as such represents a 6- to 10-fold improvement in precision. The method ensures >99.9% Mg and >97% Ti recovery, thereby allowing for the accurate determination of mass-dependent compositions with a precision better than ~60 ppm amu~(-1) for both Mg and Ti. It can further be adapted to accommodate the in-line separation of e.g. Ca, Cr, Fe, Ni, W, Mo, Ru, V, Zr and Hf from the same sample matrices. Doping tests on a synthetic Ti standard demonstrate that isobaric interference can be adequately corrected for provided that atomic ratios are Ca/Ti < 0.07, V/Ti < 0.04 and Cr/Ti < 0.005 and Zr~(2+), Mo~(2+) and Ru~(2+) have no influence on Ti measurements when atomic ratios are Zr/Ti < 0.002, Mo/Ti < 0.01 and Ru/Ti < 0.001, which is ensured by the chromatographic procedures. Magnesium and titanium isotope data for terrestrial geostandards and isotopically anomalous chondrite meteorites (OC, CR, CV, and Cl) and two CV CAIs are in excellent agreement with literature values, demonstrating the accuracy of our methods. The two CAIs plot on an extension of the mass-independent correlation line between μ~(46)Ti~* and μ~(50)Ti~* defined by inner solar system materials, suggesting residual nucleosynthetic effects in CAI.
机译:新一代质谱仪的分析改进已达到对非常小的独特自然样品进行高精度同位素分析所需的水平。陨石包裹体的多元素同位素特征可能提供对我们太阳系起源的详细了解。因此,非常需要从此类独特样品中进行多种元素的在线分离和同位素分析,但很少使用使用多收集器电感耦合等离子体源质谱(MC-ICP-MS)进行准确同位素分析所必需的当前色谱纯化程序提供。在这里,我们报告了一种新的多元素离子色谱纯化程序,专门用于从单个样品中分离非常少量的Mg(〜5μg)和Ti(0.7-1 ng)。高度同位素异常的亚毫米大小的材料,例如原始陨石中富含Ca-Al的夹杂物,可以常规分析其质量无关的μ(〜26)Mg〜*,μ〜(45)Ti〜*,μ〜 (48)Ti〜*,μ〜(49)Ti〜*和μ〜(50)Ti〜*同位素组成,其估计的外部重现性分别为4.1、11、8.8、18和12 ppm(2sd)。这些程序比以前的方法消耗的材料少得多,因此,其精度提高了6到10倍。该方法可确保> 99.9%的Mg和> 97%的Ti回收率,从而可以精确测定质量相关的成分,而Mg和Ti的精度均优于〜60 ppm amu〜(-1)。它可以进一步适合于适应例如来自相同样品基质的Ca,Cr,Fe,Ni,W,Mo,Ru,V,Zr和Hf如果原子比为Ca / Ti <0.07,V / Ti <0.04和Cr / Ti <0.005并且Zr〜(2+),Mo〜(2当原子比为Zr / Ti <0.002,Mo / Ti <0.01和Ru / Ti <0.001时,+)和Ru〜(2+)对Ti的测量没有影响,这是通过色谱程序确保的。陆地地质标准和同位素异常球粒陨石(OC,CR,CV和Cl)和两个CV CAI的镁和钛同位素数据与文献数据非常吻合,证明了我们方法的准确性。这两个CAI绘制在由内部太阳系材料定义的μ〜(46)Ti〜*和μ〜(50)Ti〜*之间的质量独立相关线的延长线上,表明了CAI中残留的核合成效应。

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  • 来源
    《Journal of Analytical Atomic Spectrometry 》 |2018年第4期| 613-628| 共16页
  • 作者单位

    Centre for Star and Planet Formation, Natural History Museum of Denmark, University of Copenhagen, DK-1350, Denmark;

    Centre for Star and Planet Formation, Natural History Museum of Denmark, University of Copenhagen, DK-1350, Denmark;

    Centre for Star and Planet Formation, Natural History Museum of Denmark, University of Copenhagen, DK-1350, Denmark;

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