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首页> 外文期刊>Journal of Analytical Atomic Spectrometry >Ultra-precise titanium stable isotope measurements by double-spike high resolution MC-ICP-MS
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Ultra-precise titanium stable isotope measurements by double-spike high resolution MC-ICP-MS

机译:通过双峰高分辨率MC-ICP-MS进行超精密的钛稳定同位素测量

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摘要

In this contribution, we present a new technique for the ultra-precise determination of titanium stable isotope composition (expressed as δ~(49)Ti or deviation of the ~(49)Ti/~(47)Ti ratio to the reference standard) of geological samples by multi-collection plasma source mass spectrometry (MC-ICPMS) using the double spike method to correct for instrumental mass bias. Tails of polyatomic spectral interferences on ~(46)Ti are accounted for by using sample-standard bracketing in high-resolution mode. Choice of ideal double and triple spike composition is investigated and results show that analytical error for a single measurement is optimised for a ~(47)Ti-~(49)Ti double spike composed of ca. 50% of each spike and mixed with ca. 52% of sample. Measurements of pure Ti solution show that internal error on single measurements of ca. 0.010‰ (95% c.i.) is attainable on δ~(49)Ti, in agreement with the error model. Due to the lack of a widely available reference isotopic standard for titanium, all results are expressed as deviations relative to newly created reference material (OL-Ti standing for Origins Laboratory - titanium) prepared from an ultra-pure titanium metal rod. A range of analytical tests demonstrates the robustness of our method. An external reproducibility of ca. 0.020‰ (2sd) is routinely achievable for Ti stable isotopes. Data for a range of basaltic rock standards as well as a subduction zone basalt reference suite is presented and show that the Ti stable isotope compositions of terrestrial basalt show resolvable variations but are overall very close to the OL-Ti reference standard. The average Ti isotopic composition of the basalts studied here is the present best estimate of the upper mantle composition; δ~(49)Ti = +0.004 ± 0.062‰ (2sd).
机译:在这项贡献中,我们提出了一种超精密测定钛稳定同位素组成的新技术(表示为δ〜(49)Ti或〜(49)Ti /〜(47)Ti比参考标准的偏差)多重采样等离子体源质谱法(MC-ICPMS)使用双尖峰法校正地质样品,以校正仪器的质量偏差。 〜(46)Ti上多原子光谱干扰的尾巴是通过在高分辨率模式下使用样本标准包围来解决的。研究了理想的双尖峰和三尖峰成分的选择,结果表明,对于由(a)组成的〜(47)Ti-〜(49)Ti双尖峰,单次测量的分析误差得到了优化。每个尖峰的50%并与大约样本的52%。纯钛溶液的测量结果表明,单次测量ca的内部误差为。与误差模型一致,在δ〜(49)Ti上可获得0.010‰(95%c.i.)。由于缺乏广泛使用的钛参考同位素标准,所有结果均表示为相对于由超纯钛金属棒制备的新创建的参考材料(代表起源实验室的OL-Ti-钛)的偏差。一系列分析测试证明了我们方法的稳健性。外部重现性约为Ti稳定同位素通常可达到0.020‰(2sd)。给出了一系列玄武岩标准品和俯冲带玄武岩参考品的数据,这些数据表明陆地玄武岩的Ti稳定同位素组成具有可分辨的变化,但总体上非常接近OL-Ti参考标准品。此处研究的玄武岩的平均Ti同位素组成是目前对上地幔成分的最佳估计。 δ〜(49)Ti = +0.004±0.062‰(2sd)。

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  • 来源
    《Journal of Analytical Atomic Spectrometry》 |2014年第8期|1444-1458|共15页
  • 作者单位

    Origins Laboratory, Department of the Geophysical Sciences and Enrico Fermi Institute, The University of Chicago, 5734 S Ellis Avenue, Chicago, IL 60637, USA ,Durham University, Department of Earth Sciences, South Road, Durham DH1 3LE, United Kingdom;

    Origins Laboratory, Department of the Geophysical Sciences and Enrico Fermi Institute, The University of Chicago, 5734 S Ellis Avenue, Chicago, IL 60637, USA;

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