分辨率、光谱窗和背景对开路傅里叶变换红外光谱多变量校准的影响

Brian K. Hart, R. James Berry, Peter R. Griffiths
{"title":"分辨率、光谱窗和背景对开路傅里叶变换红外光谱多变量校准的影响","authors":"Brian K. Hart,&nbsp;R. James Berry,&nbsp;Peter R. Griffiths","doi":"10.1002/(SICI)1520-6521(1999)3:2<117::AID-FACT7>3.0.CO;2-V","DOIUrl":null,"url":null,"abstract":"<p>The performance of CLS, PLS-2, and PLS-1 on calibration/validation sets of mixtures of five short-chain alcohols was examined as a function of resolution, spectral window, and type of background single beam to determine the feasibility of achieving automated calibrations for open-path Fourier-transform infrared (OP-FTIR) spectrometry. The backgrounds used in the study were created by ratioing actual single-beam OP-FTIR spectra. Some backgrounds were created by ratioing spectra measured at the same path length, and others were created by ratioing a long-path sample spectrum against a short-path reference. After conversion to absorbance, these background spectra provided a noise term that is representative of what is seen in actual field deployment. The absorbance spectra of mixtures of the spectra of up to five short-chain alcohols (chosen because of their spectral similarity) were added to these spectral baselines. CLS was shown to perform well only when using equidistant backgrounds and TO-16 spectral window selection, with average errors of 2–20%. CLS calibrations under other conditions tested typically produced average errors of greater than 100%. Under most conditions the measurement of OP-FTIR spectra at low (8 cm<sup>−1</sup>) resolution produced an increase in the accuracy of the determinations over higher-resolution spectra. Both PLS-1 and PLS-2 were able to predict the concentrations of the alcohols under any conditions, including short-path backgrounds, with an error of less than 5%; errors of less than 2% were achieved in most cases. The results indicate that an automated calibration system is feasible for OP-FTIR spectra measured at low resolution, even when a short-path background is used. © 1999 John Wiley &amp; Sons, Inc. Field Analyt Chem Technol 3: 117–130, 1999</p>","PeriodicalId":100527,"journal":{"name":"Field Analytical Chemistry & Technology","volume":"3 2","pages":"117-130"},"PeriodicalIF":0.0000,"publicationDate":"1999-04-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1002/(SICI)1520-6521(1999)3:2<117::AID-FACT7>3.0.CO;2-V","citationCount":"10","resultStr":"{\"title\":\"Effects of resolution, spectral window, and background on multivariate calibrations used for open-path Fourier-transform infrared spectrometry\",\"authors\":\"Brian K. Hart,&nbsp;R. James Berry,&nbsp;Peter R. Griffiths\",\"doi\":\"10.1002/(SICI)1520-6521(1999)3:2<117::AID-FACT7>3.0.CO;2-V\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p>The performance of CLS, PLS-2, and PLS-1 on calibration/validation sets of mixtures of five short-chain alcohols was examined as a function of resolution, spectral window, and type of background single beam to determine the feasibility of achieving automated calibrations for open-path Fourier-transform infrared (OP-FTIR) spectrometry. The backgrounds used in the study were created by ratioing actual single-beam OP-FTIR spectra. Some backgrounds were created by ratioing spectra measured at the same path length, and others were created by ratioing a long-path sample spectrum against a short-path reference. After conversion to absorbance, these background spectra provided a noise term that is representative of what is seen in actual field deployment. The absorbance spectra of mixtures of the spectra of up to five short-chain alcohols (chosen because of their spectral similarity) were added to these spectral baselines. CLS was shown to perform well only when using equidistant backgrounds and TO-16 spectral window selection, with average errors of 2–20%. CLS calibrations under other conditions tested typically produced average errors of greater than 100%. Under most conditions the measurement of OP-FTIR spectra at low (8 cm<sup>−1</sup>) resolution produced an increase in the accuracy of the determinations over higher-resolution spectra. Both PLS-1 and PLS-2 were able to predict the concentrations of the alcohols under any conditions, including short-path backgrounds, with an error of less than 5%; errors of less than 2% were achieved in most cases. The results indicate that an automated calibration system is feasible for OP-FTIR spectra measured at low resolution, even when a short-path background is used. © 1999 John Wiley &amp; Sons, Inc. Field Analyt Chem Technol 3: 117–130, 1999</p>\",\"PeriodicalId\":100527,\"journal\":{\"name\":\"Field Analytical Chemistry & Technology\",\"volume\":\"3 2\",\"pages\":\"117-130\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"1999-04-15\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://sci-hub-pdf.com/10.1002/(SICI)1520-6521(1999)3:2<117::AID-FACT7>3.0.CO;2-V\",\"citationCount\":\"10\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Field Analytical Chemistry & Technology\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://onlinelibrary.wiley.com/doi/10.1002/%28SICI%291520-6521%281999%293%3A2%3C117%3A%3AAID-FACT7%3E3.0.CO%3B2-V\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Field Analytical Chemistry & Technology","FirstCategoryId":"1085","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/%28SICI%291520-6521%281999%293%3A2%3C117%3A%3AAID-FACT7%3E3.0.CO%3B2-V","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 10

摘要

研究了CLS、PLS-2和PLS-1在5种短链醇混合物的校准/验证集上的性能,并将其作为分辨率、光谱窗口和背景单光束类型的函数,以确定实现开路傅里叶变换红外(OP-FTIR)光谱自动校准的可行性。研究中使用的背景是通过对实际的单束OP-FTIR光谱进行比对而产生的。一些背景是通过对相同路径长度测量的光谱进行比率来创建的,而另一些背景是通过对长路径样品光谱与短路径参考光谱进行比率来创建的。在转换为吸光度后,这些背景光谱提供了一个噪声项,代表了实际现场部署中看到的情况。最多五种短链醇的光谱混合物的吸光度光谱(因为它们的光谱相似而选择)被添加到这些光谱基线中。CLS仅在等距背景和to -16光谱窗口选择时表现良好,平均误差为2-20%。在其他条件下测试的CLS校准通常产生大于100%的平均误差。在大多数情况下,在低分辨率(8 cm−1)下测量的OP-FTIR光谱比高分辨率光谱的测定精度更高。PLS-1和PLS-2都能在任何条件下预测醇的浓度,包括短路径背景,误差小于5%;在大多数情况下,误差小于2%。结果表明,自动校准系统对于低分辨率下的OP-FTIR光谱测量是可行的,即使在使用短径背景时也是如此。©1999 John Wiley &儿子,Inc。化学工程学报(英文版),1999
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Effects of resolution, spectral window, and background on multivariate calibrations used for open-path Fourier-transform infrared spectrometry

The performance of CLS, PLS-2, and PLS-1 on calibration/validation sets of mixtures of five short-chain alcohols was examined as a function of resolution, spectral window, and type of background single beam to determine the feasibility of achieving automated calibrations for open-path Fourier-transform infrared (OP-FTIR) spectrometry. The backgrounds used in the study were created by ratioing actual single-beam OP-FTIR spectra. Some backgrounds were created by ratioing spectra measured at the same path length, and others were created by ratioing a long-path sample spectrum against a short-path reference. After conversion to absorbance, these background spectra provided a noise term that is representative of what is seen in actual field deployment. The absorbance spectra of mixtures of the spectra of up to five short-chain alcohols (chosen because of their spectral similarity) were added to these spectral baselines. CLS was shown to perform well only when using equidistant backgrounds and TO-16 spectral window selection, with average errors of 2–20%. CLS calibrations under other conditions tested typically produced average errors of greater than 100%. Under most conditions the measurement of OP-FTIR spectra at low (8 cm−1) resolution produced an increase in the accuracy of the determinations over higher-resolution spectra. Both PLS-1 and PLS-2 were able to predict the concentrations of the alcohols under any conditions, including short-path backgrounds, with an error of less than 5%; errors of less than 2% were achieved in most cases. The results indicate that an automated calibration system is feasible for OP-FTIR spectra measured at low resolution, even when a short-path background is used. © 1999 John Wiley & Sons, Inc. Field Analyt Chem Technol 3: 117–130, 1999

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
自引率
0.00%
发文量
0
×
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