State Key Laboratory for Mineral Deposits Research & Lunar and Planetary Science Institute, School of Earth Sciences and Engineering, Nanjing University, Nanjing 210023, PR China.
CAS Center for Excellence in Comparative Planetology, Hefei 230026, PR China.
Anal Chem. 2020 Apr 7;92(7):4820-4828. doi: 10.1021/acs.analchem.9b04160. Epub 2020 Mar 23.
Absolute isotopic ratios are required for isobaric interference corrections, spike calibrations, and isotopic analysis by external normalization methods. However, high-precision natural isotopic abundance data are lacking for many elements, particularly those with less than four isotopes or having isobaric isotopes with other elements. In this study, we developed a method for absolute isotope ratio analysis, which integrates the concept of the double-spike method with isotopic analysis of element pairs that have isobaric isotopes. Using multicollector inductively coupled plasma mass spectrometry (MC-ICP-MS), the isotopic composition of a sample can be derived by measuring a series of mixtures of the sample and a spike element that has an isobaric isotope with the element being analyzed. We applied this method to five pairs of elements (Ca-Ti, V-Ti, Cr-Ti, Ni-Zn, and In-Sn) and obtained the absolute isotopic ratios for Ca, V, Cr, Ni, and In, as well as the relative Ca isotopic composition. By simultaneous measurement of Ti and Ca isotopes, a quantitative relationship between the instrumental mass fractionation factors and element masses was developed. After correcting for the difference in instrumental mass fractionation factors, the obtained absolute ratios agree well with the literature data and have per mil level accuracy. This method has considerable potential in measuring the absolute isotopic ratios of elements that have isobaric isotope with other elements. Such precisely determined absolute isotopic ratios and the relationship between the instrumental mass fractionation factors and elemental masses will improve isobaric interference corrections, particularly when chemical purification is imperfect or during laser ablation analysis.
绝对同位素比对于同量异位素干扰校正、内标校准和外部归一化方法的同位素分析是必需的。然而,许多元素,特别是那些只有不到四个同位素或与其他元素具有同量异位素的元素,缺乏高精度的天然同位素丰度数据。在本研究中,我们开发了一种绝对同位素比分析方法,该方法将双内标法的概念与具有同量异位素的元素对的同位素分析相结合。使用多接收电感耦合等离子体质谱仪(MC-ICP-MS),通过测量一系列样品与具有与被分析元素同量异位素的内标元素的混合物,可以推导出样品的同位素组成。我们将该方法应用于五对元素(Ca-Ti、V-Ti、Cr-Ti、Ni-Zn 和 In-Sn),并获得了 Ca、V、Cr、Ni 和 In 的绝对同位素比以及相对 Ca 同位素组成。通过同时测量 Ti 和 Ca 同位素,建立了仪器质量分馏因子与元素质量之间的定量关系。在对仪器质量分馏因子的差异进行校正后,所得到的绝对比值与文献数据吻合良好,精度达到千分位水平。该方法在测量与其他元素具有同量异位素的元素的绝对同位素比方面具有很大的潜力。这种精确确定的绝对同位素比以及仪器质量分馏因子与元素质量之间的关系将改善同量异位素干扰校正,特别是在化学纯化不完全或在激光烧蚀分析期间。