岩石样品中铈同位素组成的精确测量

Akio Makishima, Eizo Nakamura
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引用次数: 46

摘要

报道了一种采用静态多收集质谱法测定138Ce142Ce比的高精度分析方法。该技术将数据采集时间缩短了2小时。对400个比率和改进的分析重现性为±0.002% (n-16)和精度为±0.002-0.003%。采用较大的离子束[142Ce16O为(2-7)·10−11 a],较短的数据采集时间和分析过程中18O16O比的原位测量,建立了较好的精度和再现性。为了减少空白效应对Ce同位素分析的影响,采用小型离子交换树脂床柱(4 cm长× 3 mm直径)改进了分离Ce的化学步骤,将程序总空白降低到0.04 ng,从20 mg BCR-1中提取Ce的回收率为90%。为了确认该技术的重复性,包括化学过程,从USGS标准BCR-1中分离出6个Ce同位素分析,分析重复性为±0.002%。有了这些分析精度、再现性和归一化到BCR-1,以消除任何实验室间的偏差,现在可以将LaCe同位素系统与其他同位素系统(如SmNd和RbSr)结合应用于陆地和地外样品。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Precise measurement of cerium isotope composition in rock samples

A high-precision analytical method for the measurement of 138Ce142Ce ratios is reported using static multicollection mass spectrometry. This technique reduced the data acquisition time for 2 hr. for 400 ratios and improved analytical reproducibility to ±0.002% (n-16) and precision to ±0.002–0.003%. The better precision and reproducibility were established collecting a large ion beam [142Ce16O of (2–7) · 10−11 A], short data acquisition time and in situ measurement of 18O16O ratios during the analysis.

To reduce the blank effect to the Ce isotope analysis, the chemical procedure for separation of Ce was refined using a small ion-exchange resin bed column (4 cm length × 3 mm diameter) with which the procedural total blank was lowered to 0.04 ng and the recovery yield of Ce from 20 mg BCR-1 was 90%. In order to confirm the reproducibility of this technique including the chemical procedure, six Ce isotope analyses individually separated from the USGS standard BCR-1, were carried out with an analytical reproducibility of ±0.002%.

With these analytical precision and reproducibility and normalization to BCR-1 in order to eliminate any inter-laboratory biases, it is now possible to apply the LaCe isotope system to the terrestrial and extraterrestrial samples combined with other isotope systems, such as SmNd and RbSr.

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