Xinyi Du, Biao Jin, Hans H. Richnow, Lingling Zhang, Shutao Gao, Zhiqiang Yu and Ping'an Peng
{"title":"Stable carbon isotope analysis of fluorinated organic compounds using infrared spectrometer coupled to gas chromatography†","authors":"Xinyi Du, Biao Jin, Hans H. Richnow, Lingling Zhang, Shutao Gao, Zhiqiang Yu and Ping'an Peng","doi":"10.1039/D5JA00168D","DOIUrl":null,"url":null,"abstract":"<p >Compound-specific isotope analysis (CSIA) is a powerful tool for tracing the sources and transformation processes of organic pollutants. With the rising concern on fluorinated organic compounds, there is a pressing need to develop reliable CSIA methods for determining their carbon isotopic compositions. This study developed a gas chromatography–isotope ratio infrared spectrometer (GC-IRIS) method for carbon CSIA of perfluorinated carboxylic acids and ethers. The <em>δ</em><small><sup>13</sup></small>C signatures determined by GC-IRIS were −26.1 ± 0.3‰ for heptafluorobutyric acid, −30.1 ± 0.3‰ for perfluoro-2-butyltetrahydrofuran, −30.2 ± 0.3‰ for trifluoroacetic acid, −41.0 ± 0.2‰ for perfluoropentanoic acid, −45.3 ± 0.2‰ for perfluorobutyl methyl ether, and −55.9 ± 0.4‰ for perfluoropropyl vinyl ether, respectively. Cross-validation using elemental analysis–isotope ratio mass spectrometry (EA-IRMS) confirmed consistency between the two methods, showing good agreement in the <em>δ</em><small><sup>13</sup></small>C values, supporting the reliability of the GC-IRIS method. The method was further applied to resolve carbon isotope fractionation during volatilization of perfluorobutyl methyl ether and perfluoro-2-butyltetrahydrofuran, both exhibiting inverse carbon isotope effects. This work reports a novel and robust GC-IRIS method for carbon CSIA of fluorinated compounds, highlighting the potential for characterizing isotopic signatures and environmental behaviors of different fluorinated organic compounds.</p>","PeriodicalId":81,"journal":{"name":"Journal of Analytical Atomic Spectrometry","volume":" 8","pages":" 1940-1945"},"PeriodicalIF":3.1000,"publicationDate":"2025-07-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Analytical Atomic Spectrometry","FirstCategoryId":"92","ListUrlMain":"https://pubs.rsc.org/en/content/articlelanding/2025/ja/d5ja00168d","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
Compound-specific isotope analysis (CSIA) is a powerful tool for tracing the sources and transformation processes of organic pollutants. With the rising concern on fluorinated organic compounds, there is a pressing need to develop reliable CSIA methods for determining their carbon isotopic compositions. This study developed a gas chromatography–isotope ratio infrared spectrometer (GC-IRIS) method for carbon CSIA of perfluorinated carboxylic acids and ethers. The δ13C signatures determined by GC-IRIS were −26.1 ± 0.3‰ for heptafluorobutyric acid, −30.1 ± 0.3‰ for perfluoro-2-butyltetrahydrofuran, −30.2 ± 0.3‰ for trifluoroacetic acid, −41.0 ± 0.2‰ for perfluoropentanoic acid, −45.3 ± 0.2‰ for perfluorobutyl methyl ether, and −55.9 ± 0.4‰ for perfluoropropyl vinyl ether, respectively. Cross-validation using elemental analysis–isotope ratio mass spectrometry (EA-IRMS) confirmed consistency between the two methods, showing good agreement in the δ13C values, supporting the reliability of the GC-IRIS method. The method was further applied to resolve carbon isotope fractionation during volatilization of perfluorobutyl methyl ether and perfluoro-2-butyltetrahydrofuran, both exhibiting inverse carbon isotope effects. This work reports a novel and robust GC-IRIS method for carbon CSIA of fluorinated compounds, highlighting the potential for characterizing isotopic signatures and environmental behaviors of different fluorinated organic compounds.