Selective Extraction of PCBs from Fish Tissue Using Accelerated Solvent Extraction
Applications | 2013 | Thermo Fisher ScientificInstrumentation
Accelerated solvent extraction (ASE) offers rapid and automated sample preparation for extraction of persistent organic pollutants like PCBs from complex matrices. The removal of lipids and coextractives in fish tissue is critical to ensure accurate and interference-free chromatographic analysis.
This work evaluates a selective ASE approach combining a nonpolar solvent with in-cell alumina sorbent to extract PCBs from fish tissue while minimizing lipid coextraction. The goal is to compare recoveries, precision, and cleanup requirements against conventional nonselective ASE followed by postextraction treatments like sulfuric acid and size-exclusion chromatography.
Sample preparation involves mixing 3 g of homogenized fish tissue reference material (ground whole carp, CARP-1) with diatomaceous earth dispersant, drying to remove moisture, and loading into a 33 mL ASE cell containing cellulose filters and 5 g acid-activated alumina. Extraction uses hexane at 100 °C and 1500 psi for two static cycles of 5 minutes each, totaling 17 minutes per sample. Extracts are analyzed directly by GC-ECD without further cleanup, following U.S. EPA Method 8081. Nonselective extractions use methylene chloride/acetone (1:1) with a postextraction sulfuric acid cleanup for comparison.
Selective ASE with in-cell alumina achieved PCB recoveries largely within certified 95% confidence intervals and exhibited superior precision (RSDs generally <5%). Chromatograms showed removal of lipid interferences compared to nonselective hexane or dichloromethane/acetone extractions, eliminating the need for acid or size-exclusion cleanup. Conventional ASE with sulfuric acid cleanup delivered more variable recoveries and occasional out-of-range values.
Advancements may include integration with on-line cleanup modules, exploration of alternative sorbents for a broader range of analytes, and coupling ASE with mass spectrometry for improved detection limits. Scaling selective ASE to handle higher sample throughput and varied matrices could broaden its industrial and regulatory adoption.
Selective accelerated solvent extraction using a hexane solvent and in-cell alumina sorbent provides a fast, automated, and effective method for PCB analysis in fish tissues. It eliminates extensive lipid cleanup, delivers reliable recoveries, and streamlines chromatographic workflows.
GC, Sample Preparation
IndustriesFood & Agriculture
ManufacturerThermo Fisher Scientific
Summary
Significance of the Topic
Accelerated solvent extraction (ASE) offers rapid and automated sample preparation for extraction of persistent organic pollutants like PCBs from complex matrices. The removal of lipids and coextractives in fish tissue is critical to ensure accurate and interference-free chromatographic analysis.
Objectives and Study Overview
This work evaluates a selective ASE approach combining a nonpolar solvent with in-cell alumina sorbent to extract PCBs from fish tissue while minimizing lipid coextraction. The goal is to compare recoveries, precision, and cleanup requirements against conventional nonselective ASE followed by postextraction treatments like sulfuric acid and size-exclusion chromatography.
Methodology and Instrumentation
Sample preparation involves mixing 3 g of homogenized fish tissue reference material (ground whole carp, CARP-1) with diatomaceous earth dispersant, drying to remove moisture, and loading into a 33 mL ASE cell containing cellulose filters and 5 g acid-activated alumina. Extraction uses hexane at 100 °C and 1500 psi for two static cycles of 5 minutes each, totaling 17 minutes per sample. Extracts are analyzed directly by GC-ECD without further cleanup, following U.S. EPA Method 8081. Nonselective extractions use methylene chloride/acetone (1:1) with a postextraction sulfuric acid cleanup for comparison.
Used Instrumentation
- Thermo Scientific Dionex ASE 200 Accelerated Solvent Extractor (11–33 mL cells)
- Analytical balance
- Gas chromatograph with electron-capture detector
Key Results and Discussion
Selective ASE with in-cell alumina achieved PCB recoveries largely within certified 95% confidence intervals and exhibited superior precision (RSDs generally <5%). Chromatograms showed removal of lipid interferences compared to nonselective hexane or dichloromethane/acetone extractions, eliminating the need for acid or size-exclusion cleanup. Conventional ASE with sulfuric acid cleanup delivered more variable recoveries and occasional out-of-range values.
Benefits and Practical Applications
- Substantially reduces sample preparation time from hours to minutes
- Minimizes solvent usage and manual cleanup steps
- Enhances analytical accuracy by selective removal of lipids
- Maintains high recoveries and reproducible results for trace PCB analysis in fish tissues
Future Trends and Applications
Advancements may include integration with on-line cleanup modules, exploration of alternative sorbents for a broader range of analytes, and coupling ASE with mass spectrometry for improved detection limits. Scaling selective ASE to handle higher sample throughput and varied matrices could broaden its industrial and regulatory adoption.
Conclusion
Selective accelerated solvent extraction using a hexane solvent and in-cell alumina sorbent provides a fast, automated, and effective method for PCB analysis in fish tissues. It eliminates extensive lipid cleanup, delivers reliable recoveries, and streamlines chromatographic workflows.
Reference
- U.S. EPA Method 8081: Organochlorine Pesticides and PCBs by Gas Chromatography
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