Title of article :
Polymeric ionic liquid coatings versus commercial solid-phase microextraction coatings for the determination of volatile compounds in cheeses
Author/Authors :
Trujillo-Rodrيguez، نويسنده , , Marيa J. and Yu، نويسنده , , Honglian and Cole، نويسنده , , William T.S. and Ho، نويسنده , , Tien D. and Pino، نويسنده , , Verَnica and Anderson، نويسنده , , Jared L. and Afonso، نويسنده , , Ana M.، نويسنده ,
Issue Information :
ماهنامه با شماره پیاپی سال 2014
Abstract :
The extraction performance of four polymeric ionic liquid (PIL)-based solid-phase microextraction (SPME) coatings has been studied and compared to that of commercial SPME coatings for the extraction of 16 volatile compounds in cheeses. The analytes include 2 free fatty acids, 2 aldehydes, 2 ketones and 10 phenols and were determined by headspace (HS)-SPME coupled to gas chromatography (GC) with flame-ionization detection (FID). The PIL-based coatings produced by UV co-polymerization were more efficient than PIL-based coatings produced by thermal AIBN polymerization. Partition coefficients of analytes between the sample and the coating (Kfs) were estimated for all PIL-based coatings and the commercial SPME fiber showing the best performance among the commercial fibers tested: carboxen–polydimethylsyloxane (CAR–PDMS). For the PIL-based fibers, the highest Kfs value (1.96±0.03) was obtained for eugenol. The normalized calibration slope, which takes into account the SPME coating thickness, was also used as a simpler approximate tool to compare the nature of the coating within the determinations, with results entirely comparable to those obtained with estimated Kfs values. The PIL-based materials obtained by UV co-polymerization containing the 1-vinyl-3-hexylimidazolium chloride IL monomer and 1,12-di(3-vinylimiazolium)dodecane dibromide IL crosslinker exhibited the best performance in the extraction of the select analytes from cheeses. Despite a coating thickness of only 7 µm, this copolymeric sorbent coating was capable of quantitating analytes in HS-SPME in a 30 to 2000 µg L−1 concentration range, with correlation coefficient (R) values higher than 0.9938, inter-day precision values (as relative standard deviation in %) varying from 6.1 to 20%, and detection limits down to 1.6 µg L−1.
Keywords :
Ionic liquids , Polymeric ionic liquids , Solid-phase microextraction , volatile compounds , Gas-Chromatography