Full correction of the self-absorption of laser-induced plasma beryllium emissions via sample preparation

IF 3.2 2区 化学 Q1 SPECTROSCOPY Spectrochimica Acta Part B: Atomic Spectroscopy Pub Date : 2024-06-01 DOI:10.1016/j.sab.2024.106958
Hui Chen , Zhuhai Chen , Ronggen Luo , Yuehua Chen , Shuolei Wei , Guanqing Mo , Tao Xu
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Abstract

Self-absorption effect is always encountered in laser-induced breakdown spectroscopy (LIBS) and immediately distorts the calibration curves especially for the elemental determination of complex materials. With the aim to provide an expeditious approach for LIBS measurements susceptible to self-absorption effect, an exploratory study for sample preparation by powder mixing is implemented, and the self-absorption of laser-induced plasma beryllium emissions is investigated as a function of the dilution factor. For comparison, boric acid and wax powder are separately used as typical binding agent to mix with beryl powder to produce two sets of pressed pellets with sequential gradient of beryllium content variation. For the resonant lines most prone to self-absorption of Be II emission doublet at 313.042 nm and 313.107 nm, the beryllium spectral line shapes can be directly regulated and improved in the case of both sets of pellets as the dilution factor increases. In addition, the self-absorption effect for the strongly emitting beryllium spectral lines is further assessed by calculating the self-absorption coefficients based on the radiation transport equation. With regard to the both types of binder as diluent, when the dilution factor for beryl increases to 10 with a weight percent of 0.386% for beryllium in the pellet, the SA values may exponentially increase in general to around 0.8 and eventually asymptotically approaches to 1 without exception. Thus the self-absorption effect of laser-induced beryl plasma emissions can be readily overcome with sample preparation by powder mixing. By contrast with laser pulse irradiance in the present work, the dilution factor for powder mixing plays a dominant role in eliminating self-absorption effect. This research proposes a potentially effective approach to reduce self-absorption in laser-induced plasma emissions.

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通过样品制备对激光诱导等离子体铍发射的自吸收进行全面修正
自吸收效应在激光诱导击穿光谱(LIBS)中经常出现,会立即扭曲校准曲线,尤其是在测定复杂材料的元素含量时。为了给易受自吸收效应影响的激光诱导击穿光谱测量提供一种快速方法,我们对通过粉末混合制备样品进行了探索性研究,并研究了激光诱导等离子体铍发射的自吸收与稀释因子的函数关系。为了进行比较,分别使用硼酸和蜡粉作为典型的结合剂,与绿柱石粉末混合,生产出两套铍含量依次梯度变化的压制颗粒。在波长为 313.042 nm 和 313.107 nm 的铍 II 发射双线中,最容易发生自吸收的共振线,随着稀释因子的增加,两组颗粒的铍谱线形状都能得到直接调节和改善。此外,根据辐射传输方程计算自吸收系数,进一步评估了强发射铍谱线的自吸收效应。对于这两种作为稀释剂的粘合剂,当绿柱石的稀释因子增加到 10,铍在颗粒中的重量百分比为 0.386% 时,SA 值一般会呈指数增长,达到 0.8 左右,最终无一例外地渐近于 1。因此,激光诱导的绿柱石等离子体发射的自吸收效应可以通过粉末混合的样品制备方法轻松克服。与本研究中的激光脉冲辐照度相比,混合粉末的稀释因子在消除自吸收效应方面起着主导作用。这项研究提出了一种减少激光诱导等离子体发射自吸收的潜在有效方法。
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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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