Before reliable near infrared spectroscopic analysis - the critical sampling proviso. Part 1: Generalised theory of sampling

IF 16.4 1区 化学 Q1 CHEMISTRY, MULTIDISCIPLINARY
K. Esbensen, N. Abu-Khalaf
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引用次数: 1

Abstract

Non-representative sampling of materials, lots and processes intended for near infrared (NIR) analysis is often contributing hidden additions to the full Measurement Uncertainty (MUtotal = TSE + TAENIR). The Total Sampling Error (TSE) can dominate over the Total Analytical Error (TAENIR) by factors ranging from 5 to 10 to even 25 times, depending on material heterogeneity and the specific sampling procedures employed to produce the minuscule aliquot, which is the only material analysed. This review (Parts 1 and 2), extensively referenced with easily available complementing literature, presents a brief of all sampling uncertainty elements in the “lot-to-aliquot” pathway, which must be identified and correctly managed (eliminated or maximally reduced) in order to achieve, and to be able to document, fully minimised MUtotal. The more irregular and pervasive the heterogeneity, the higher the number of increments needed to reach ‘fit-for-purpose representativity’. A particular focus is necessary regarding the sampling bias, which is fundamentally different from the well-known analytical bias. Whereas the latter can easily be subjected to bias correction, the sampling bias is non-correctable by any posteori means, notably not by chemometrics, nor statistics. Instead, all sampling operations must be designed to exclude the so-called Incorrect Sampling Errors (ISE), which are the hidden bias-generating agents. The key element in this endeavour is representative sampling and sub-sampling before analysis, as laid out by the Theory of Sampling (TOS), which is presented here in a novel compact fashion along with a complement of selected examples and demonstrations. TOS includes a safeguard facility, termed the Replication Experiment (RE), which enables estimation of the total sampling-plus-analysis uncertainty level (MUtotal) associated with NIR analysis (the RE is, for practical and logistical reasons, found in Part 2). Neglecting the TSE effects from the before-analysis domain is lack of due diligence. TOS to the fore!
在进行可靠的近红外光谱分析之前——关键采样条件。第1部分:抽样的一般理论
用于近红外(NIR)分析的材料、批次和过程的非代表性采样通常会对整个测量不确定度(MUtotal = TSE + TAENIR)造成隐藏的增加。总抽样误差(TSE)可以在总分析误差(TAENIR)上占主导地位,其因素范围从5到10甚至25倍,这取决于材料的异质性和用于产生微小等同物的特定抽样程序,这是唯一被分析的材料。本综述(第1部分和第2部分)广泛引用了易于获得的补充文献,简要介绍了“批量到相同”路径中所有采样不确定因素,这些因素必须被识别和正确管理(消除或最大限度地减少),以实现并能够记录完全最小化MUtotal。异质性越不规则和普遍,达到“符合目的的代表性”所需的增量数量就越高。需要特别关注抽样偏差,它与众所周知的分析偏差有着根本的不同。尽管后者可以很容易地进行偏差校正,但抽样偏差是无法通过任何后验方法校正的,特别是不能通过化学计量学或统计学。相反,所有的采样操作都必须设计成排除所谓的不正确采样误差(ISE),这是隐藏的偏差产生代理。这项工作的关键要素是分析前的代表性抽样和子抽样,如抽样理论(TOS)所述,在这里以一种新颖紧凑的方式呈现,同时补充了选定的示例和演示。TOS包括一个被称为复制实验(RE)的保障设施,它可以估计与近红外分析相关的总采样加分析不确定性水平(MUtotal)(出于实际和后勤原因,RE在第2部分中找到)。忽略分析前领域的TSE影响是缺乏尽职调查的。加油!
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Accounts of Chemical Research
Accounts of Chemical Research 化学-化学综合
CiteScore
31.40
自引率
1.10%
发文量
312
审稿时长
2 months
期刊介绍: Accounts of Chemical Research presents short, concise and critical articles offering easy-to-read overviews of basic research and applications in all areas of chemistry and biochemistry. These short reviews focus on research from the author’s own laboratory and are designed to teach the reader about a research project. In addition, Accounts of Chemical Research publishes commentaries that give an informed opinion on a current research problem. Special Issues online are devoted to a single topic of unusual activity and significance. Accounts of Chemical Research replaces the traditional article abstract with an article "Conspectus." These entries synopsize the research affording the reader a closer look at the content and significance of an article. Through this provision of a more detailed description of the article contents, the Conspectus enhances the article's discoverability by search engines and the exposure for the research.
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