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以锶为例,MC ICP-MS测量同位素丰度比的评估策略与不确定度计算

Evaluation strategies and uncertainty calculation of isotope amount ratios measured by MC ICP-MS on the example of Sr.

作者信息

Horsky Monika, Irrgeher Johanna, Prohaska Thomas

出版信息

Anal Bioanal Chem. 2016 Jan;408(2):351-67. doi: 10.1007/s00216-015-9003-9.

Abstract

This paper critically reviews the state-of-the-art of isotope amount ratio measurements by solution-based multi-collector inductively coupled plasma mass spectrometry (MC ICP-MS) and presents guidelines for corresponding data reduction strategies and uncertainty assessments based on the example of n((87)Sr)/n((86)Sr) isotope ratios. This ratio shows variation attributable to natural radiogenic processes and mass-dependent fractionation. The applied calibration strategies can display these differences. In addition, a proper statement of uncertainty of measurement, including all relevant influence quantities, is a metrological prerequisite. A detailed instructive procedure for the calculation of combined uncertainties is presented for Sr isotope amount ratios using three different strategies of correction for instrumental isotopic fractionation (IIF): traditional internal correction, standard-sample bracketing, and a combination of both, using Zr as internal standard. Uncertainties are quantified by means of a Kragten spreadsheet approach, including the consideration of correlations between individual input parameters to the model equation. The resulting uncertainties are compared with uncertainties obtained from the partial derivatives approach and Monte Carlo propagation of distributions. We obtain relative expanded uncertainties (U rel; k = 2) of n((87)Sr)/n((86)Sr) of < 0.03 %, when normalization values are not propagated. A comprehensive propagation, including certified values and the internal normalization ratio in nature, increases relative expanded uncertainties by about factor two and the correction for IIF becomes the major contributor.

摘要

本文批判性地综述了基于溶液的多接收电感耦合等离子体质谱法(MC ICP-MS)测量同位素丰度比的技术现状,并以(n(^{87}Sr)/n(^{86}Sr))同位素比值为例,给出了相应数据处理策略和不确定度评估的指导方针。该比值显示出因自然放射性过程和质量相关分馏导致的变化。所应用的校准策略能够体现这些差异。此外,对测量不确定度进行恰当表述,包括所有相关影响量,是计量学的前提条件。本文针对(Sr)同位素丰度比,使用三种不同的仪器同位素分馏(IIF)校正策略:传统内标校正、标准-样品分段分析以及二者结合(以(Zr)作为内标),给出了计算合成不确定度的详细指导程序。不确定度通过Kragten电子表格方法进行量化,包括考虑模型方程中各个输入参数之间的相关性。将所得不确定度与通过偏导数方法和蒙特卡洛分布传播获得的不确定度进行比较。当不传播归一化值时,我们得到(n(^{87}Sr)/n(^{86}Sr))的相对扩展不确定度((U_{rel});(k = 2))小于(0.03%)。全面传播,包括认证值和自然界中的内部归一化比值,会使相对扩展不确定度增加约两倍,并且IIF校正成为主要贡献因素。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ec99/4709391/3b5ac7c12435/216_2015_9003_Fig1_HTML.jpg

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