Forward-Scattering and Multiple-Scattering Sources of Errors in UV-Visible Spectroscopy of Microspheres.

IF 6.7 1区 化学 Q1 CHEMISTRY, ANALYTICAL Analytical Chemistry Pub Date : 2024-11-25 DOI:10.1021/acs.analchem.4c04912
Azizeh Alidoust Ghatar, Baptiste Auguié, Eric C Le Ru
{"title":"Forward-Scattering and Multiple-Scattering Sources of Errors in UV-Visible Spectroscopy of Microspheres.","authors":"Azizeh Alidoust Ghatar, Baptiste Auguié, Eric C Le Ru","doi":"10.1021/acs.analchem.4c04912","DOIUrl":null,"url":null,"abstract":"<p><p>Conventional UV-visible spectroscopy instruments measure the extinction spectrum of solutions in a transmission configuration. Because of the finite (nonzero) acceptance angle in detection, errors due to forward scattering and multiple scattering can be introduced when measuring scattering samples. We here experimentally quantify these errors using polystyrene spheres of different sizes for two representative analytical/research UV-visible instruments, one based on a single-beam diode array and the other on a double-beam scanning configuration. The measured spectra for particles larger than 1 μm are shown to differ between the two instruments, even at low concentrations, and also vary with concentration (in contradiction with the Beer-Lambert law). We show that systematic errors in the range of 10-40% are common in such measurements. We propose a model accounting for both forward- and multiple-scattering errors and demonstrate its agreement with our experimental results. This model could reduce systematic errors in measurements of scattering samples by up to 40%.</p>","PeriodicalId":27,"journal":{"name":"Analytical Chemistry","volume":" ","pages":""},"PeriodicalIF":6.7000,"publicationDate":"2024-11-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Analytical Chemistry","FirstCategoryId":"92","ListUrlMain":"https://doi.org/10.1021/acs.analchem.4c04912","RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, ANALYTICAL","Score":null,"Total":0}
引用次数: 0

Abstract

Conventional UV-visible spectroscopy instruments measure the extinction spectrum of solutions in a transmission configuration. Because of the finite (nonzero) acceptance angle in detection, errors due to forward scattering and multiple scattering can be introduced when measuring scattering samples. We here experimentally quantify these errors using polystyrene spheres of different sizes for two representative analytical/research UV-visible instruments, one based on a single-beam diode array and the other on a double-beam scanning configuration. The measured spectra for particles larger than 1 μm are shown to differ between the two instruments, even at low concentrations, and also vary with concentration (in contradiction with the Beer-Lambert law). We show that systematic errors in the range of 10-40% are common in such measurements. We propose a model accounting for both forward- and multiple-scattering errors and demonstrate its agreement with our experimental results. This model could reduce systematic errors in measurements of scattering samples by up to 40%.

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
微球紫外可见光谱分析中的正向散射和多重散射误差源。
传统的紫外-可见光谱仪测量的是透射结构中溶液的消光光谱。由于检测中的接受角是有限的(非零),因此在测量散射样品时可能会引入正向散射和多重散射造成的误差。在此,我们使用两种具有代表性的分析/研究紫外可见光仪器(一种基于单光束二极管阵列,另一种基于双光束扫描配置),使用不同大小的聚苯乙烯球对这些误差进行了实验量化。结果表明,即使在低浓度条件下,两台仪器对大于 1 μm 的颗粒所测得的光谱也不尽相同,而且还随浓度的变化而变化(与比尔-朗伯定律相矛盾)。我们的研究表明,在这种测量中,10%-40% 的系统误差是很常见的。我们提出了一个同时考虑前向散射和多重散射误差的模型,并证明了该模型与实验结果的一致性。该模型可将散射样品测量中的系统误差减少多达 40%。
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 去求助
来源期刊
Analytical Chemistry
Analytical Chemistry 化学-分析化学
CiteScore
12.10
自引率
12.20%
发文量
1949
审稿时长
1.4 months
期刊介绍: Analytical Chemistry, a peer-reviewed research journal, focuses on disseminating new and original knowledge across all branches of analytical chemistry. Fundamental articles may explore general principles of chemical measurement science and need not directly address existing or potential analytical methodology. They can be entirely theoretical or report experimental results. Contributions may cover various phases of analytical operations, including sampling, bioanalysis, electrochemistry, mass spectrometry, microscale and nanoscale systems, environmental analysis, separations, spectroscopy, chemical reactions and selectivity, instrumentation, imaging, surface analysis, and data processing. Papers discussing known analytical methods should present a significant, original application of the method, a notable improvement, or results on an important analyte.
期刊最新文献
How Machine Learning and Gas Chromatography-Ion Mobility Spectrometry Form an Optimal Team for Benchtop Volatilomics Protein-Induced Electrochemiluminescence Enhancement of Tetraphenylvinyl Derivatives for Ultrasensitive Bioanalysis Ultrahigh Resolving Power Ion Mobility Spectrometry with a Simple Pulser Circuitry Blood Screening of Femtomole Level Multiple Alzheimer's Disease Biomarkers by Metal Isotopic DNA Walkers. Development of a Platform for High-Resolution Ion Mobility Separations Coupled with Messenger Tagging Infrared Spectroscopy for High-Precision Structural Characterizations.
×
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
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 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 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1