AI Article Synopsis

  • Hexabromocyclododecane (HBCDD) is a brominated flame retardant flagged for elimination due to its environmental persistence and potential harmful effects.
  • The study successfully isolated and characterized the six main HBCDD stereoisomers using innovative enantioselective supercritical fluid chromatography methods.
  • The research demonstrates the effectiveness of packed column supercritical fluid chromatography as an eco-friendly technique for analyzing environmental contaminants, achieving baseline separation of all HBCDD enantiomers.

Article Abstract

Hexabromocyclododecane (HBCDD) is an additive brominated flame retardant which has been listed in Annex A of the Stockholm Convention for elimination of production and use. It has been reported to persist in the environment and has the potential for enantiomer-specific degradation, accumulation, or both, making enantioselective analyses increasingly important. The six main stereoisomers of technical HBCDD (i.e., the (+) and (-) enantiomers of α-, β-, and γ-HBCDD) were separated and isolated for the first time using enantioselective packed column supercritical fluid chromatography (pSFC) separation methods on a preparative scale. Characterization was completed using published chiral liquid chromatography (LC) methods and elution profiles, as well as X-ray crystallography, and the isolated fractions were definitively identified. Additionally, the resolution of the enantiomers, along with two minor components of the technical product (δ- and ε-HBCDD), was investigated on an analytical scale using both LC and pSFC separation techniques, and changes in elution order were highlighted. Baseline separation of all HBCDD enantiomers was achieved by pSFC on an analytical scale using a cellulose-based column. The described method emphasizes the potential associated with pSFC as a green method of isolating and analyzing environmental contaminants of concern.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6273052PMC
http://dx.doi.org/10.3390/molecules21111509DOI Listing

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