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从X射线光谱中提取特征线强度时的准确性限制。

Limitations to Accuracy in Extracting Characteristic Line Intensities From X-Ray Spectra.

作者信息

Statham Peter J

机构信息

Oxford Instruments Analytical Limited, High Wycombe, HP12 3SE, UK.

出版信息

J Res Natl Inst Stand Technol. 2002 Dec 1;107(6):531-46. doi: 10.6028/jres.107.045. Print 2002 Nov-Dec.

Abstract

The early development of quantitative electron probe microanalysis, first using crystal spectrometers, then energy dispersive x-ray spectrometers (EDXS), demonstrated that elements could be detected at 0.001 mass fraction level and major concentrations measured within 2 % relative uncertainty. However, during this period of extensive investigation and evaluation, EDXS detectors were not able to detect x rays below 1 keV and all quantitative analysis was performed using a set of reference standards measured on the instrument. Now that EDXS systems are often used without standards and are increasingly being used to analyse elements using lines well below 1 keV, accuracy can be considerably worse than is documented in standard textbooks. Spectrum processing techniques found most applicable to EDXS have now been integrated into total system solutions and can give excellent results on selected samples. However, the same techniques fail in some applications because of a variety of instrumental effects. Prediction of peak shape, width and position for every characteristic line and measurement of background intensity is complicated by variations in response from system to system and with changing count rate. However, with an understanding of the fundamental sources of error, even a total system can be tested like a "black box" in areas where it is most likely to fail and thus establish the degree of confidence that should apply in the intended application. This approach is particularly important when the microanalysis technique is applied at lower electron beam voltages where the extraction of line intensities is complicated by extreme peak overlap and higher background levels.

摘要

定量电子探针显微分析的早期发展,先是使用晶体光谱仪,之后是能量色散X射线光谱仪(EDXS),结果表明可以检测到质量分数低至0.001的元素,并且能够在2%的相对不确定度范围内测量主要元素的浓度。然而,在这一广泛研究和评估阶段,EDXS探测器无法检测到能量低于1keV的X射线,所有定量分析都是使用在仪器上测量的一组参考标准进行的。如今,EDXS系统常常在不使用标准的情况下使用,并且越来越多地用于分析能量远低于1keV谱线的元素,其准确性可能比标准教科书所记载的要差得多。现已发现最适用于EDXS的光谱处理技术已被集成到整个系统解决方案中,并且在选定的样品上能够给出出色的结果。然而,由于各种仪器效应,同样的技术在某些应用中会失效。由于不同系统之间以及随着计数率变化响应存在差异,预测每条特征谱线的峰形、宽度和位置以及测量背景强度变得很复杂。然而,了解了误差的基本来源后,即使是整个系统也可以在最可能出现故障的区域像“黑匣子”一样进行测试,从而确定在预期应用中应有的置信度。当在较低电子束电压下应用显微分析技术时,这种方法尤为重要,因为在这种情况下,谱线强度的提取会因极端的峰重叠和更高的背景水平而变得复杂。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/26c1/4863855/3ba8053393a7/j76staf1.jpg

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