Chromite ore: X-ray fluorescence spectral analysis of Kβ and L-lines by WD-XRF

IF 1.7 4区 化学 Q3 CHEMISTRY, MULTIDISCIPLINARY
Ashok Kumar Maurya, Ashish Kumar Pandey, Piyali Deb Barman
{"title":"Chromite ore: X-ray fluorescence spectral analysis of Kβ and L-lines by WD-XRF","authors":"Ashok Kumar Maurya, Ashish Kumar Pandey, Piyali Deb Barman","doi":"10.1007/s12039-024-02280-8","DOIUrl":null,"url":null,"abstract":"<p>This work delves into the utility of chromium’s X-ray fluorescence (XRF) lines for the analysis of chromite ores, employing a wavelength-dispersive XRF spectrometer. The CrL<i>α</i><sub>1,2</sub> and CrL<i>β</i><sub>1</sub> fluorescence lines, despite not involving electronic transitions from valence to K-core shell, offer substantial insights into the valence state of chromium. This study examines these relatively unexplored but potentially valuable lines and compares them with the CrK<i>β</i> series fluorescence lines. Intriguingly, our investigation reveals striking differences in the L-line fluorescence spectra between metallic chromium (Cr(0)), chromite ores (Fe, Mg)Cr<sub>2</sub>O<sub>4</sub>, and K<sub>2</sub>Cr<sub>2</sub>O<sub>7</sub>. Chemical shifts and peak shapes emerge as key discriminators, surpassing the sensitivity of the CrK<i>β</i><sub>1,3</sub> lines. Notably, the chemical shifts of L-lines are amplified, showcasing a clear trend: Cr(III) exhibits a larger shift than Cr(VI), mirroring the pattern observed in the K<i>β</i>-lines. The fluorescence peak shapes of L<i>α</i><sub>1,2</sub> and L<i>β</i><sub>1</sub> for metallic chromium and chromite ores (both have unpaired 3d-electrons) are similar, whereas those of K<sub>2</sub>Cr<sub>2</sub>O<sub>7</sub> differ considerably in peak shape, indicating that unpaired 3d-electrons influence these peaks. A linear relationship was found between the area under the curve ratio for L<i>α</i><sub>1,2</sub> and L<i>β</i><sub>1</sub> and the valence state of chromium.</p><h3 data-test=\"abstract-sub-heading\">Graphical Abstract</h3>\n","PeriodicalId":616,"journal":{"name":"Journal of Chemical Sciences","volume":null,"pages":null},"PeriodicalIF":1.7000,"publicationDate":"2024-05-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Chemical Sciences","FirstCategoryId":"92","ListUrlMain":"https://doi.org/10.1007/s12039-024-02280-8","RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 0

Abstract

This work delves into the utility of chromium’s X-ray fluorescence (XRF) lines for the analysis of chromite ores, employing a wavelength-dispersive XRF spectrometer. The CrLα1,2 and CrLβ1 fluorescence lines, despite not involving electronic transitions from valence to K-core shell, offer substantial insights into the valence state of chromium. This study examines these relatively unexplored but potentially valuable lines and compares them with the CrKβ series fluorescence lines. Intriguingly, our investigation reveals striking differences in the L-line fluorescence spectra between metallic chromium (Cr(0)), chromite ores (Fe, Mg)Cr2O4, and K2Cr2O7. Chemical shifts and peak shapes emerge as key discriminators, surpassing the sensitivity of the CrKβ1,3 lines. Notably, the chemical shifts of L-lines are amplified, showcasing a clear trend: Cr(III) exhibits a larger shift than Cr(VI), mirroring the pattern observed in the Kβ-lines. The fluorescence peak shapes of Lα1,2 and Lβ1 for metallic chromium and chromite ores (both have unpaired 3d-electrons) are similar, whereas those of K2Cr2O7 differ considerably in peak shape, indicating that unpaired 3d-electrons influence these peaks. A linear relationship was found between the area under the curve ratio for Lα1,2 and Lβ1 and the valence state of chromium.

Graphical Abstract

Abstract Image

铬铁矿:利用 WD-XRF 对 Kβ 和 L 线进行 X 射线荧光光谱分析
这项研究利用波长色散 XRF 光谱仪,深入研究了铬的 X 射线荧光 (XRF) 线在分析铬铁矿石中的用途。CrLα1,2和CrLβ1荧光线尽管不涉及从价层到K核壳的电子跃迁,但却为了解铬的价态提供了大量信息。本研究考察了这些相对未开发但具有潜在价值的荧光线,并将它们与 CrKβ 系列荧光线进行了比较。有趣的是,我们的研究揭示了金属铬(Cr(0))、铬铁矿石(Fe, Mg)Cr2O4 和 K2Cr2O7 之间 L 线荧光光谱的显著差异。化学位移和峰形是关键的判别因素,其灵敏度超过了 CrKβ1,3 线。值得注意的是,L 线的化学位移被放大,呈现出明显的趋势:Cr(III)的化学位移比 Cr(VI) 的大,这与在 Kβ 线中观察到的模式如出一辙。金属铬和铬矿石(都有未配对的 3d 电子)的 Lα1,2 和 Lβ1 荧光峰形状相似,而 K2Cr2O7 的荧光峰形状差别很大,这表明未配对的 3d 电子影响了这些荧光峰。发现 Lα1,2 和 Lβ1 的曲线下面积比与铬的价态之间存在线性关系。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
Journal of Chemical Sciences
Journal of Chemical Sciences CHEMISTRY, MULTIDISCIPLINARY-
CiteScore
3.10
自引率
5.90%
发文量
107
审稿时长
1 months
期刊介绍: Journal of Chemical Sciences is a monthly journal published by the Indian Academy of Sciences. It formed part of the original Proceedings of the Indian Academy of Sciences – Part A, started by the Nobel Laureate Prof C V Raman in 1934, that was split in 1978 into three separate journals. It was renamed as Journal of Chemical Sciences in 2004. The journal publishes original research articles and rapid communications, covering all areas of chemical sciences. A significant feature of the journal is its special issues, brought out from time to time, devoted to conference symposia/proceedings in frontier areas of the subject, held not only in India but also in other countries.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信