Heating-, Cooling- and Vacuum-Assisted Solid-Phase Microextraction (HCV-SPME) for Efficient Sampling of Environmental Pollutants in Complex Matrices

This research introduces a novel solid-phase microextraction technology, in which the features of heating of sample, cooling of sorbent, and extraction under vacuum condition have been merged. Heating-, cooling- and vacuum-assisted solid-phase microextraction (HCV-SPME) method was developed as an ef...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Chromatographia 2020-04, Vol.83 (4), p.531-540
Hauptverfasser: Ghiasvand, Alireza, Yazdankhah, Fatemeh, Paull, Brett
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
Beschreibung
Zusammenfassung:This research introduces a novel solid-phase microextraction technology, in which the features of heating of sample, cooling of sorbent, and extraction under vacuum condition have been merged. Heating-, cooling- and vacuum-assisted solid-phase microextraction (HCV-SPME) method was developed as an efficient solution for the direct extraction of volatile and semi-volatiles species in complex solid samples. HCV-SPME was coupled with an in-needle capillary adsorption trap (HCV-INCAT) and applied to the direct extraction of polycyclic aromatic hydrocarbons (PAHs) within soil samples. It consisted of polythiophene/carboxylic acid modified multi-walled carbon nanotube nanocomposite, which was synthesized and wall-coated within a platinized stainless-steel needle via electropolymerization. The influential experimental variables (desorption conditions, sample temperature, adsorption temperature, sampling flow rate, and vacuum level) on the extraction efficiency were optimized. The developed HCV-INCAT technique was used in conjunction with GC-FID and applied for the extraction and determination of PAHs in contaminated soil samples, closely matching with those obtained using a validated ultrasonic-assisted solvent extraction procedure. Under the optimal conditions, linear dynamic ranges, limits of detection, and relative standard deviations were obtained 0.007–5 µg g −1 , 8–20 pg g −1 , and 7.1–12.1%, respectively, for direct extraction of naphthalene, fluorene, phenanthrene, fluoranthene, and pyrene from solid samples.
ISSN:0009-5893
1612-1112
DOI:10.1007/s10337-020-03869-0