Impact of sample preparation on bitumen content measurement using laser-induced breakdown spectroscopy

IF 3.2 2区 化学 Q1 SPECTROSCOPY Spectrochimica Acta Part B: Atomic Spectroscopy Pub Date : 2024-11-22 DOI:10.1016/j.sab.2024.107083
Shubho Mohajan , Foroogh Mehravaran , Sakila Ansari , Liam Droog , Nicholas F. Beier , Fatima Keserwan , Yingchao Huang , Abdul Bais , Robert Fedosejevs , Mohamed Gamal El-Din , Amina E. Hussein
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Abstract

The impact of sample preparation on bitumen content measurement using LIBS was investigated by collecting spectra from wet and dry tailings. A multivariate data analysis model was developed using optimal wavelength selection for bitumen content classification and prediction in tailings. Wet tailings can be classified into three classes (low, medium, and high bitumen) with 12.1 % error, while dry tailings have a classification error of 6.1 %. Quantitative analysis showed a bitumen content prediction error of 4.7 % for wet tailings and 8.9 % for dry tailings. Wet tailings showed a 1.8–2.5 times improvement in the limit of detection range compared to dry tailings. Plasma density and crater size measurements revealed that plasma density fluctuation was 2.7 times lower in wet tailings due to consistent crater formation from laser-tailings interaction. The lower plasma density fluctuation indicates a stable mass ablation for wet samples, which is attributed as the primary reason for significant LIBS performance improvement on wet tailings.

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样品制备对激光诱导击穿光谱测量沥青含量的影响
通过采集干尾矿和湿尾矿的光谱,研究了样品制备对LIBS测定沥青含量的影响。建立了基于最佳波长选择的多变量数据分析模型,用于尾矿中沥青含量的分类和预测。湿尾矿可分为低、中、高沥青三类,误差为12.1%,干尾矿的分类误差为6.1%。定量分析表明,湿尾砂沥青含量预测误差为4.7%,干尾砂沥青含量预测误差为8.9%。湿尾砂检测范围的极限是干尾砂的1.8 ~ 2.5倍。等离子体密度和弹坑尺寸测量表明,湿尾砂中等离子体密度波动比湿尾砂低2.7倍,这是由于激光与尾砂相互作用形成的一致的弹坑。较低的等离子体密度波动表明湿样质量烧蚀稳定,这是湿尾砂LIBS性能显著提高的主要原因。
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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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