Bedoukian   RussellIPM   RussellIPM   Piezoelectric Micro-Sprayer


Home
Animal Taxa
Plant Taxa
Semiochemicals
Floral Compounds
Semiochemical Detail
Semiochemicals & Taxa
Synthesis
Control
Invasive spp.
References

Abstract

Guide

Alphascents
Pherobio
InsectScience
E-Econex
Counterpart-Semiochemicals
Print
Email to a Friend
Kindly Donate for The Pherobase

« Previous AbstractComparison of extraction techniques and mass spectrometric ionization modes in the analysis of wine volatile carbonyls    Next AbstractMultiple automated headspace in-tube extraction for the accurate analysis of relevant wine aroma compounds and for the estimation of their relative liquid-gas transfer rates »

J Chromatogr A


Title:Automated and quantitative headspace in-tube extraction for the accurate determination of highly volatile compounds from wines and beers
Author(s):Zapata J; Mateo-Vivaracho L; Lopez R; Ferreira V;
Address:"Laboratory for Flavor Analysis and Enology, Institute of Engineering of Aragon, I3A. Department of Analytical Chemistry, Faculty of Sciences, University of Zaragoza, 50009 Zaragoza, Spain"
Journal Title:J Chromatogr A
Year:2012
Volume:20120121
Issue:
Page Number:1 - 7
DOI: 10.1016/j.chroma.2012.01.037
ISSN/ISBN:1873-3778 (Electronic) 0021-9673 (Linking)
Abstract:"An automatic headspace in-tube extraction (ITEX) method for the accurate determination of acetaldehyde, ethyl acetate, diacetyl and other volatile compounds from wine and beer has been developed and validated. Method accuracy is based on the nearly quantitative transference of volatile compounds from the sample to the ITEX trap. For achieving that goal most methodological aspects and parameters have been carefully examined. The vial and sample sizes and the trapping materials were found to be critical due to the pernicious saturation effects of ethanol. Small 2 mL vials containing very small amounts of sample (20 muL of 1:10 diluted sample) and a trap filled with 22 mg of Bond Elut ENV resins could guarantee a complete trapping of sample vapors. The complete extraction requires 100 x 0.5 mL pumping strokes at 60 degrees C and takes 24 min. Analytes are further desorbed at 240 degrees C into the GC injector under a 1:5 split ratio. The proportion of analytes finally transferred to the trap ranged from 85 to 99%. The validation of the method showed satisfactory figures of merit. Determination coefficients were better than 0.995 in all cases and good repeatability was also obtained (better than 7% in all cases). Reproducibility was better than 8.3% except for acetaldehyde (13.1%). Detection limits were below the odor detection thresholds of these target compounds in wine and beer and well below the normal ranges of occurrence. Recoveries were not significantly different to 100%, except in the case of acetaldehyde. In such a case it could be determined that the method is not able to break some of the adducts that this compound forms with sulfites. However, such problem was avoided after incubating the sample with glyoxal. The method can constitute a general and reliable alternative for the analysis of very volatile compounds in other difficult matrixes"
Keywords:Beer/*analysis Equipment Design Gas Chromatography-Mass Spectrometry/methods Limit of Detection Sensitivity and Specificity Solid Phase Microextraction/*instrumentation Volatile Organic Compounds/*analysis Wine/*analysis;
Notes:"MedlineZapata, Julian Mateo-Vivaracho, Laura Lopez, Ricardo Ferreira, Vicente eng Research Support, Non-U.S. Gov't Validation Study Netherlands 2012/02/22 J Chromatogr A. 2012 Mar 23; 1230:1-7. doi: 10.1016/j.chroma.2012.01.037. Epub 2012 Jan 21"

 
Back to top
 
Citation: El-Sayed AM 2024. The Pherobase: Database of Pheromones and Semiochemicals. <http://www.pherobase.com>.
© 2003-2024 The Pherobase - Extensive Database of Pheromones and Semiochemicals. Ashraf M. El-Sayed.
Page created on 19-12-2024