scholarly journals Optimization of Solid-Phase Microextraction for the Gas Chromatography/Mass Spectrometry Analysis of Persistent Organic Pollutants

2004 ◽  
Vol 87 (4) ◽  
pp. 1021-1027 ◽  
Author(s):  
Ana Gago-Martínez ◽  
María J Nogueiras ◽  
Sandra Rellán ◽  
Juan Prado ◽  
María F Alpendurada ◽  
...  

Abstract In this work, solid-phase microextraction (SPME) has been applied as an alternative for the selective extraction of 3 polybrominated diphenyl ethers (PBDEs), 2,2′,4,4′-tetrabromodiphenyl ether (PBDE-47); 2,2′,4,4′,5-pentabromodiphenyl ether (PBDE-99); and 2,2′,4,4′,6-pentabromodiphenyl ether (PBDE-100), and 2 alkylphenols, 4-tert-OP and 4-NP, prior to their analysis by gas chromatography/mass spectrometry (GC/MS). The advantages of this technique are mainly its simplicity, cost-effectiveness, and time-saving sample preparation, as well as being a solvent-free technique. With the aim of optimizing the conditions for an efficient extraction of the studied compounds, different fiber coatings and the main parameters affecting the extraction procedure have been evaluated. The results obtained showed a good linearity in the range of concentrations investigated, and adequate relative standard deviation values were found according to the range accepted for SPME. Recovery values were in the range of 78–108%, and good detection and quantitation limits at ppt levels were obtained for both methods, allowing the determination of the selected compounds in samples at trace levels. The results obtained clearly show the potential of SPME for efficient concentration of the target compounds and also demonstrate the reliability of this extraction technique for their GC/MS analysis.

2000 ◽  
Vol 83 (5) ◽  
pp. 1082-1086 ◽  
Author(s):  
Maurizio Guidotti

Abstract A method was developed for the selective determination of Se4+ in drinkable water by solid-phase microextraction (SPME) and gas chromatography/mass spectrometry (GC/MS). Se4+ was selectively derivatized to ethane, 1,1′-selenobis by reaction with sodium tetraethylborate, extracted by the SPME fiber, and determined by GC/MS. Both headspace (HS)–SPME and direct SPME were studied. The method requires only a few milliliters of sample and 20 min for completion. At 2.0 μg/L concentration, the relative standard deviation was 10.1% for HS–SPME and 9.1% for direct SPME. For HS–SPME, the theoretical detection limit was 81 ng/L and 166 ng/L for direct SPME. The recovery rate was 95%. The method was used to determine Se4+ in 10 tap water samples.


2019 ◽  
Vol 14 (6) ◽  
pp. 1934578X1985912
Author(s):  
Andreas Douros ◽  
Anastasia Christopoulou ◽  
Stefanos Kikionis ◽  
Konstantinos Nikolaou ◽  
Helen Skaltsa

In the present study, the heartwood and the sapwood of a thick wood disc from a dated Cedrus brevifolia trunk, and the resin were analyzed for their volatile components. All samples were subjected to headspace solid-phase microextraction followed by gas chromatography mass spectrometry analysis. The main constituents were β-himachalene (22.2 %) in heartwood and (25.0 %) in sapwood, and α-pinene (37.8 %) in resin.


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