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Optimised accelerated solvent extraction of PCBs and PAHs from compost
Authors:Rahel C. Brändli  Thomas Kupper  Franz X. Stadelmann  Joseph Tarradellas
Affiliation:1. Ecole Polytechnique Fédérale de Lausanne (EPFL) , Laboratory of Environmental Chemistry and Ecotoxicology (CECOTOX), Faculty of Architecture, Civil and Environmental Engineering , CH-1015 Lausanne, Switzerland;2. Agroscope FAL Reckenholz , Swiss Federal Institute for Agroecology and Agriculture , Reckenholzstrasse 191, CH-8046 Zürich, Switzerland;3. EAWAG , Aquatic Research, Urban Water Management , CH-6800 Dübendorf, Switzerland;4. Agroscope FAL Reckenholz , Swiss Federal Institute for Agroecology and Agriculture , Reckenholzstrasse 191, CH-8046 Zürich, Switzerland;5. Ecole Polytechnique Fédérale de Lausanne (EPFL) , Laboratory of Environmental Chemistry and Ecotoxicology (CECOTOX), Faculty of Architecture, Civil and Environmental Engineering , CH-1015 Lausanne, Switzerland
Abstract:This study is the first thorough method optimisation for accelerated solvent extraction (ASE) of polychlorinated biphenyls (PCBs) and polycyclic aromatic hydrocarbons (PAHs) from chemically dried compost. For PCBs, optimised solvent composition, temperature, pressure, number of static cycles, duration, and flush volume were as follows: toluene/acetone 1?:?3 (v/v), 120°C, 2000?psi, 3?×?5?min, and 50%, respectively. Limits of quantification and method precision were between 0.16 and 2.46?µg?kg?1 dw and 6–17% respectively for individual PCBs. Absolute recoveries of isotope-labelled extraction standards used for each of the analytes ranged from 65 to 105% and relative recoveries were between 85 and 99%. The method proofed to be robust and was successfully applied to different compost samples.

The optimisation of PAHs extraction was performed and resulted in the following conditions: solvent: hexane/acetone 1/3 (v:v), temperature: 140°C, pressure: 1500?psi, extraction time: 3?×?5?min, and 50% flush volume. Limits of detection and method precision for individual PAHs were between 1.1 and 37.2?µg?kg?1?dw and 12–34% respectively. Absolute and relative recoveries ranged from 24 to 68% and from 85 to 99%, respectively. Optimal extraction conditions for PAHs were more difficult to determine due to the inhomogeneous distribution of PAHs in samples. However, the method appeared to be feasible and suggestions for further improvements are presented.
Keywords:ASE  Polychlorinated biphenyls  Polycyclic aromatic hydrocarbons  Sample preparation
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