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Optimization of microwave-assisted solvent extraction of polycyclic aromatic hydrocarbons in marine sediments using a microwave extraction system with high-performance liquid chromatography-fluorescence detection and gas chromatography-mass spectrometry
- Source :
- Journal of Chromatography A. 723:259-271
- Publication Year :
- 1996
- Publisher :
- Elsevier BV, 1996.
-
Abstract
- In the present study, a microwave-assisted solvent extraction (MASE) technique using a microwave extraction system (MES) has been developed for the extraction of polycyclic aromatic hydrocarbons (PAHs) from marine sediment. The optimum MASE conditions can be obtained by performing the mixed-level orthogonal array design (OAD) procedure. A comparison between the Soxhlet extraction method and the MASE technique showed that although both techniques gave comparable results on certified reference materials (CRM) HS-4 and HS-6, the MASE technique allows the use of less solvent and is also time-saving and cost-effective without affecting its extraction efficiency. The optimum MASE technique was coupled to two analytical techniques: high-performance liquid chromatography (HPLC) with both ultraviolet (UV) and fluorescence detectors and gas chromatography-mass spectrometry (GC-MS) for the qualitative and quantitative screening of PAHs in CRM and “real world” samples. Recoveries of PAHs from two CRMs were all above 73.3%. The concentration of PAHs in marine sediment collected from primary industrial areas was between 0.03 and 0.35 μg/g on a dry weight basis.
- Subjects :
- chemistry.chemical_classification
Chromatography
Organic Chemistry
Extraction (chemistry)
Analytical chemistry
General Medicine
Mass spectrometry
Biochemistry
High-performance liquid chromatography
Analytical Chemistry
Solvent
Hydrocarbon
Certified reference materials
chemistry
Gas chromatography
Gas chromatography–mass spectrometry
Subjects
Details
- ISSN :
- 00219673
- Volume :
- 723
- Database :
- OpenAIRE
- Journal :
- Journal of Chromatography A
- Accession number :
- edsair.doi...........919a12062086f4be9d0c47f2a027ff94
- Full Text :
- https://doi.org/10.1016/0021-9673(95)00882-9