Determining the sources of (sub)permil-level inaccuracy during laser ablation-MC-ICPMS boron isotope measurements of carbonates†

IF 3.1 2区 化学 Q2 CHEMISTRY, ANALYTICAL
Douglas Coenen, David Evans, Hana Jurikova, Matthew Dumont, James Rae and Wolfgang Müller
{"title":"Determining the sources of (sub)permil-level inaccuracy during laser ablation-MC-ICPMS boron isotope measurements of carbonates†","authors":"Douglas Coenen, David Evans, Hana Jurikova, Matthew Dumont, James Rae and Wolfgang Müller","doi":"10.1039/D4JA00154K","DOIUrl":null,"url":null,"abstract":"<p >Recent developments in spatially-resolved boron isotopic analysis using laser ablation as a means of sample introduction to MC-ICPMS instruments (LA-MC-ICPMS) increasingly allow researchers to explore the spatial heterogeneity of the boron isotopic composition of a range of geochemical applications, for example in palaeoclimatology and mantle petrology. However, previous work has shown that a diffuse interference centred near <small><sup>10</sup></small>B, when measuring samples with a calcium-rich matrix, can significantly bias especially the measurement on <small><sup>10</sup></small>B, affecting the accuracy of boron isotope measurements. Although several correction approaches have yielded sufficiently accurate analyses of <em>δ</em><small><sup>11</sup></small>B in calcium carbonate, the root cause of this interference is still not fully resolved. Here, we explore the various potential sources of inaccuracy in boron isotope measurements made using (LA-)MC-ICPMS by experimenting with dry and wet plasma conditions, in both solution and laser ablation mode (in the former case, our solution (Ca–Mg)/B ratios broadly mimic those found in natural samples). In solution mode, we find that irrespective of wet or dry plasma conditions, the introduction of a Ca-containing matrix yields a baseline up to ∼4 and ∼14 times higher around <em>m</em>/<em>z</em> ≈ 10 for wet and dry plasma conditions, respectively, compared to both a Mg-only matrix and lack of matrix. In order to explore this further, we performed mass scans around <em>m</em>/<em>z</em> ≈ 10 during laser ablation of different carbonates with varying matrix [Ca]. These show that the <em>m</em>/<em>z</em> ≈ 10 interference scales linearly with a mixture of the calcium content of the analyte matrix and <small><sup>40</sup></small>Ar<small><sup>4+</sup></small> ion beam intensity, as previously hypothesised. Moreover, by experimenting with different plasma loading scenarios during the ablation of CaCO<small><sub>3</sub></small>, <em>i.e.</em> varying laser spot sizes, we find that permil-level inaccuracies in <em>δ</em><small><sup>11</sup></small>B may occur when the analyte ablated mass is significantly different than that of the standard used to calibrate instrumental mass bias. This is important given that we also show that different commonly-used reference materials ablate at very different rates, which illustrates the need for a careful standardisation approach irrespective of broader matrix effects when sub-permil level accuracy and precision are desirable when utilising LA-MC-ICPMS.</p>","PeriodicalId":81,"journal":{"name":"Journal of Analytical Atomic Spectrometry","volume":" 10","pages":" 2409-2420"},"PeriodicalIF":3.1000,"publicationDate":"2024-07-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://pubs.rsc.org/en/content/articlepdf/2024/ja/d4ja00154k?page=search","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Analytical Atomic Spectrometry","FirstCategoryId":"92","ListUrlMain":"https://pubs.rsc.org/en/content/articlelanding/2024/ja/d4ja00154k","RegionNum":2,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, ANALYTICAL","Score":null,"Total":0}
引用次数: 0

Abstract

Recent developments in spatially-resolved boron isotopic analysis using laser ablation as a means of sample introduction to MC-ICPMS instruments (LA-MC-ICPMS) increasingly allow researchers to explore the spatial heterogeneity of the boron isotopic composition of a range of geochemical applications, for example in palaeoclimatology and mantle petrology. However, previous work has shown that a diffuse interference centred near 10B, when measuring samples with a calcium-rich matrix, can significantly bias especially the measurement on 10B, affecting the accuracy of boron isotope measurements. Although several correction approaches have yielded sufficiently accurate analyses of δ11B in calcium carbonate, the root cause of this interference is still not fully resolved. Here, we explore the various potential sources of inaccuracy in boron isotope measurements made using (LA-)MC-ICPMS by experimenting with dry and wet plasma conditions, in both solution and laser ablation mode (in the former case, our solution (Ca–Mg)/B ratios broadly mimic those found in natural samples). In solution mode, we find that irrespective of wet or dry plasma conditions, the introduction of a Ca-containing matrix yields a baseline up to ∼4 and ∼14 times higher around m/z ≈ 10 for wet and dry plasma conditions, respectively, compared to both a Mg-only matrix and lack of matrix. In order to explore this further, we performed mass scans around m/z ≈ 10 during laser ablation of different carbonates with varying matrix [Ca]. These show that the m/z ≈ 10 interference scales linearly with a mixture of the calcium content of the analyte matrix and 40Ar4+ ion beam intensity, as previously hypothesised. Moreover, by experimenting with different plasma loading scenarios during the ablation of CaCO3, i.e. varying laser spot sizes, we find that permil-level inaccuracies in δ11B may occur when the analyte ablated mass is significantly different than that of the standard used to calibrate instrumental mass bias. This is important given that we also show that different commonly-used reference materials ablate at very different rates, which illustrates the need for a careful standardisation approach irrespective of broader matrix effects when sub-permil level accuracy and precision are desirable when utilising LA-MC-ICPMS.

Abstract Image

确定激光烧蚀-MC-ICPMS 碳酸盐硼同位素测量过程中(亚) permil 级误差的来源
利用激光烧蚀作为将样品引入 MC-ICPMS 仪器(LA-MC-ICPMS)的一种手段,空间分辨硼同位素分析的最新发展越来越多地使研究人员能够探索一系列地球化学应用(例如古气候学和地幔岩石学)中硼同位素组成的空间异质性。然而,以往的工作表明,在测量富含钙基质的样品时,以 10B 附近为中心的弥散干扰会严重偏差 10B 的测量,从而影响硼同位素测量的准确性。尽管有几种校正方法可以充分准确地分析碳酸钙中的δ11B,但这种干扰的根本原因仍未完全解决。在这里,我们通过在溶液模式和激光烧蚀模式(在前一种情况下,我们的溶液(Ca-Mg)/硼比率与天然样品中的比率大致相同)下的干和湿等离子体条件下进行实验,探讨了使用(LA-)MC-ICPMS 进行硼同位素测量不准确的各种潜在原因。在溶液模式下,我们发现无论在干湿等离子体条件下,还是在湿等离子体条件下,引入含钙基质后,m/z ≈ 10 附近的基线分别比纯镁基质和不含镁基质的基线高出 4 和 14 倍。为了进一步探讨这个问题,我们在激光烧蚀不同碳酸盐(基质[Ca]不同)的过程中,对 m/z ≈ 10 附近进行了质量扫描。结果表明,m/z ≈ 10 干扰基本上与分析基质的钙含量和 40Ar4+ 离子束强度呈线性关系,这与之前的假设一致。此外,通过对 CaCO3 烧蚀过程中的不同等离子加载情况(即不同的激光光斑尺寸)进行实验,我们发现当烧蚀的分析物质量明显大于用于校准仪器质量偏差的标准质量时,δ11B 的永久级误差可能会出现。这一点非常重要,因为我们还发现不同的常用参考材料的消融速度非常不同,这说明在使用 LA-MC-ICPMS 时,如果希望获得亚毫微米级的准确度和精确度,就需要采用谨慎的标准化方法,而不考虑更广泛的基质效应。
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
CiteScore
6.20
自引率
26.50%
发文量
228
审稿时长
1.7 months
期刊介绍: Innovative research on the fundamental theory and application of spectrometric techniques.
×
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