Title: Isolation and Analysis of Polycyclic Aromatic Hydrocarbons from Natural Water Using Accelerated Solvent Extraction Followed by Gas Chromatography-mass Spectrometry
Authors: OLIVELLA Angels
Citation: TALANTA vol. 69 no. 1 p. 267-275
Publisher: ELSEVIER SCIENCE BV
Publication Year: 2006
JRC N°: JRC32560
URI: http://publications.jrc.ec.europa.eu/repository/handle/JRC32560
Type: Articles in Journals
Abstract: An innovative analytical procedure for the analysis of polycyclic aromatic hydrocarbons (PAHs) from large-volume water samples is presented. It involves sample preparation, sampling and the elution process in an automated continuous procedure involving the ASE technique. Prior to sampling, a XAD-2 resin column is prepared on the basis of a commercial accelerated solvent extraction (ASE) cartridge so that the resin bed is permanently fixed. Then, the XAD column inside the ASE cartridge is cleaned and conditioned. The sampling procedure involves conventional filtration with subsequent isolation of dissolved PAHs on an XAD-2 resin contained in the ASE cartridge. After sampling, the XAD-2 resin content inside the cartridge is eluted by ASE without any further sample preparation and subsequently reused. In order to validate the procedure, the PAHs were isolated from water samples from the Lake Maggiore (North of Italy) using both XAD-2 resin adsorption and hexane liquid–liquid extraction according to the International Standard Methodology ISO 17993. The mean percentages of deviation between concentrations obtained by both methodologies range from 6% for benzo(a)pyrene to 15% for fluoranthene and benzo(b,k)fluoranthene. Compared to the traditional techniques, this procedure offers numerous practical advantages: easy to perform, fast, savings in solvent volume and in time, all steps are fully automated thus avoiding any XAD-2 resin manipulation during and between steps and moreover, low detection limits were provided (0.001 ng l−1 for chrysene, benzo(b,k)fluoranthene, benzo(a)pyrene, dibenz(a,h)anthracene, benzo(g,h,i)perylene and indeno(1,2,3-cd)pyrene, and 0.01 ng l−1 for acenaphthylene and fluoranthene).
JRC Institute:Institute for Environment and Sustainability

Files in This Item:
There are no files associated with this item.


Items in repository are protected by copyright, with all rights reserved, unless otherwise indicated.