Selective enrichment procedures for the determination of polychlorinated biphenyls and polycyclic aromatic hydrocarbons in environmental samples by gel permeation chromatography

1988 ◽  
Vol 456 ◽  
pp. 155-164 ◽  
Author(s):  
P. Fernández ◽  
C. Porte ◽  
D. Barceló ◽  
J.M. Bayona ◽  
J. Albaigés
Molecules ◽  
2020 ◽  
Vol 25 (16) ◽  
pp. 3727
Author(s):  
Łukasz Dąbrowski

For complex matrices such as environmental samples, there is usually a problem with not fully resolved peaks during GC/MS analysis. The PARADISe computer program (based on the PARFAC2 model) allows the identification of peaks using the deconvoluted mass spectra and the NIST MS library. The number of repetitions required by this software (at least five) is a real limitation for the determination of semi-volatile compounds, like polycyclic aromatic hydrocarbons, polychlorinated biphenyls, and organic pesticides in environmental samples. In this work, the method to overcome this condition was proposed and evaluated. The sets of the five files required by PARADISe were prepared by mathematically modifying the original GC/MS chromatograms obtained for the standard mixture (C = 2 µg/mL of 40 compounds) and real sample extracts (soil samples with different total organic carbon content and one cardboard extract) spiked with standards. Total average match factor for all the substances identified in a standard mixture was 874 (near 900—“excellent match”), and for all the substances in the real samples, it was 786 (near 800—“good match”). The results from PARADISe were comparable to those obtained with other programs: AMDIS (NIST) and MassHunter (Agilent), tested also in this work. PARADISe software can be effectively used for chromatogram deconvolution and substance identification.


2005 ◽  
Vol 88 (4) ◽  
pp. 1247-1254 ◽  
Author(s):  
Sandra Martinez-López ◽  
Asuncion Morales-Noé ◽  
Agustin Pastor-Garcia ◽  
Angel Morales-Rubio ◽  
Miguel de la Guardia

Abstract The determination of 15 polycyclic aromatic hydrocarbons (PAHs) in olive oil samples has been improved in order to obtain a fast methodology with a low limit of detection through the combination of liquid–liquid extraction with acetonitrile and preparative gel permeation chromatography (GPC) prior to the injection of purified extracts into a C18 column. Acetonitrile–water was used as the mobile phase with a gradient from 50 to 95%, w/w, acetonitrile in 30 min. The oven temperature was maintained at 15°C, and fluorometric detection was made at a fixed excitation wavelength of 264 nm and variable, optimal emission wavelength for each analyte ranging from 352 nm for 11-H-benzo(b)fluorene to 500 nm for indeno(1,2,3-cd)pyrene. Recovery for all the compounds studied varied from 75 to 111%, and limit of detection values from 0.05 ng/g for benzo(k)fluoranthene to 0.48 ng/g for indeno(1,2,3-cd)pyrene, corresponding to 0.09 ng/g benzo(a)pyrene. Results were compared with those obtained by liquid–liquid extraction followed by a cleanup on silica and a direct GPC treatment of oil samples diluted in dichloromethane, 2 other methodologies that are appropriate for quantifying PAHs in olive oils. However, the proposed method improves the determination limits, reduces the time of analysis, and provides a highly stable baseline for sample chromatograms.


2008 ◽  
Vol 31 (10) ◽  
pp. 1787-1796 ◽  
Author(s):  
Wilson A. Lopes ◽  
Gisele O. da Rocha ◽  
Pedro A. de P. Pereira ◽  
Fábio S. Oliveira ◽  
Luiz. S. Carvalho ◽  
...  

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