使用酸消化生物参考材料进行全反射 X 射线荧光测量时,优化样品制备过程中的干燥方法

IF 3.2 2区 化学 Q1 SPECTROSCOPY
Paula Kasprzyk, Paweł M. Wróbel, Wiktoria Tokarczyk, Magdalena Szczerbowska-Boruchowska
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引用次数: 0

摘要

样品处理是采用全反射 X 射线荧光 (TXRF) 方法进行分析的关键步骤之一。然而,为测量准备样品本身会带来许多困难,并在测量结果中引入许多可见误差。在这项工作中,我们试图验证在生物样本的情况下,应用的样本干燥程序是否会造成这种影响。为此,我们对苹果叶、番茄叶、牡蛎组织和牛肝这四种参考材料进行了酸消化。为每种参考材料制备了 10 个重复样本,并使用以下五种方法进行干燥:层流室(LFC)、100 毫巴真空室(VC)、250 瓦红外灯(IR)和使用两种加热温度(即 45 ℃ 和 75 ℃)的热板(HP45、HP75)。结果表明,在测量多元素样品时,干燥方法的选择对 TXRF 的最终定量结果没有明显影响。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Optimisation of the drying method during sample preparation for total reflection X-ray fluorescence measurements using acid digested biological reference materials

Optimisation of the drying method during sample preparation for total reflection X-ray fluorescence measurements using acid digested biological reference materials
Sample processing is one of the key steps in the analysis by the Total Reflection X-ray Fluorescence (TXRF) method. However, the preparation of the sample itself for measurement can present many difficulties and introduce many errors visible in the measurement results. In this work, we have attempted to verify whether, in the case of biological specimens, such an effect can be caused by the applied sample drying procedure. For this purpose samples of four reference materials - apple leaves, tomato leaves, oyster tissue and beef liver, were acid digested. Ten replicates were prepared for each reference material and dried using five methods: laminar flow chamber (LFC), 100 mbar vacuum chamber (VC), 250 W infrared lamp (IR) and hot-plate with the use of two heating temperatures i.e. 45 °C and 75 °C (HP45, HP75). The results showed that, in the context of measuring a multi-element sample, the choice of drying method has no significant effect on the final TXRF quantitative results.
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来源期刊
CiteScore
6.10
自引率
12.10%
发文量
173
审稿时长
81 days
期刊介绍: Spectrochimica Acta Part B: Atomic Spectroscopy, is intended for the rapid publication of both original work and reviews in the following fields: Atomic Emission (AES), Atomic Absorption (AAS) and Atomic Fluorescence (AFS) spectroscopy; Mass Spectrometry (MS) for inorganic analysis covering Spark Source (SS-MS), Inductively Coupled Plasma (ICP-MS), Glow Discharge (GD-MS), and Secondary Ion Mass Spectrometry (SIMS). Laser induced atomic spectroscopy for inorganic analysis, including non-linear optical laser spectroscopy, covering Laser Enhanced Ionization (LEI), Laser Induced Fluorescence (LIF), Resonance Ionization Spectroscopy (RIS) and Resonance Ionization Mass Spectrometry (RIMS); Laser Induced Breakdown Spectroscopy (LIBS); Cavity Ringdown Spectroscopy (CRDS), Laser Ablation Inductively Coupled Plasma Atomic Emission Spectroscopy (LA-ICP-AES) and Laser Ablation Inductively Coupled Plasma Mass Spectrometry (LA-ICP-MS). X-ray spectrometry, X-ray Optics and Microanalysis, including X-ray fluorescence spectrometry (XRF) and related techniques, in particular Total-reflection X-ray Fluorescence Spectrometry (TXRF), and Synchrotron Radiation-excited Total reflection XRF (SR-TXRF). Manuscripts dealing with (i) fundamentals, (ii) methodology development, (iii)instrumentation, and (iv) applications, can be submitted for publication.
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