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合并校准的原理使得在使用高分辨率连续光源火焰原子吸收光谱法(HR-CS FAAS)测定时,钠(Na)、镁(Mg)和镍(Ni)测量不确定度之间实现完全对应。

The principle of pooled calibrations delivers full correspondence between uncertainties of measurements of Na, Mg and Ni when determined using HR-CS FAAS.

作者信息

Andersen Jens E T, Moemedi Keaboletse, Katse Kebabonye

机构信息

Botswana International University of Science and Technology, Department of Chemical and Forensic Sciences, Plot 10071, Boseja Ward, Private Bag 016, Palapye, Botswana.

出版信息

Heliyon. 2023 Feb 8;9(2):e13562. doi: 10.1016/j.heliyon.2023.e13562. eCollection 2023 Feb.

Abstract

Methods for determination of elements in various types of samples are generally considered to be very precise and highly accurate. For reliable analysis of elements Na, Mg and Ni in food samples is it worthwhile to perform an extensive method validation of high-resolution continuum source flame atomic absorption spectrometry (HR-CS FAAS) according to the principle of pooled calibrations (PoPC). Under routine laboratory conditions of analysis, elevated levels of relative uncertainty of measurement reaching values of more than 50% were detected, which jeopardized the validity of results, even when the measurements in the present study were performed with samples of tap water and borehole water. Comparison of relative uncertainties with corresponding literature results indicates that sample-signal differences may be due to detector noise rather than specimen variations.

摘要

各类样品中元素的测定方法通常被认为非常精确且高度准确。对于食品样品中钠、镁和镍元素的可靠分析,按照合并校准(PoPC)原则对高分辨率连续光源火焰原子吸收光谱法(HR-CS FAAS)进行广泛的方法验证是否值得。在常规实验室分析条件下,检测到测量的相对不确定度水平升高,达到超过50%的值,这危及了结果的有效性,即使本研究中的测量是使用自来水和井水样品进行的。将相对不确定度与相应的文献结果进行比较表明,样品信号差异可能是由于检测器噪声而非样品变化所致。

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