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, R. James Berry, 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 & 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, R. James Berry, 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 & 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