Abstract
Due to the similarity in chemical and physicochemical properties between analytes (chlorinated fatty acids) and matrix compounds (nonchlorinated fatty acids), conventional cleanup procedures were not successful in analysis of chlorinated fatty acids in extracts of freshwater fish. A new approach was devised of utilizing reversed‐phase high performance liquid chromatography (HPLC) for its high separation power, and the halogen specific detector (XSD) for its high selectivity for organochlorine. The bulk of nonchlorinated matrix was removed by HPLC fractionation, and target chlorinated analytes were selectively enriched. The enrichment effect was assessed by a universal detector, a flame ionization detector (FID). Methyl esters of chlorinated fatty acids were completely nondetectable prior to HPLC fractionation, but were present as moderate or small, yet discernible, peaks after the HPLC enrichment. This enrichment method is efficient with good selectivity, reproducibility, and predictability.
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
More From: Journal of Liquid Chromatography & Related Technologies
Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.