Spike(软件开发)
生物系统
计算机科学
先验与后验
同位素
样品(材料)
基质(化学分析)
分馏
算法
分析化学(期刊)
化学
色谱法
量子力学
生物
认识论
软件工程
物理
哲学
作者
Martijn Klaver,Christopher D. Coath
摘要
Ever‐increasing precision in isotope ratio measurements requires a concomitant small bias within and between laboratories. The double spike technique is the most suitable method to obtain reliable isotope composition data that are accurately corrected for instrumental mass fractionation. Compared with other methods, such as sample‐calibrator bracketing (SCB), only the double spike technique can correct for all sources of fractionation after equilibration of the sample with the double spike, such as that incurred during chemical separation and measurement. In addition, it is not dependent on a priori assumptions of perfect matrix matching of samples to reference materials or quantitative recovery of the sample through the chemical separation procedure to yield accurate results. In this review article, we present a detailed discussion of the merits of the double spike technique, how to design and calibrate a suitable double spike and analytical strategies. Our objective is to offer a step‐by‐step introduction to the use of the double spike technique in order to lower potential barriers that researchers new to the subject might face, such that double spiking will replace SCB as the measurement method of choice.
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