Multi-residue Analysis of PAHs, PCBs and OCPs on an Agilent J&W FactorFour VF-5ms GC Column
Applications | 2010 | Agilent TechnologiesInstrumentation
Multi-residue gas chromatography–mass spectrometry (GC–MS) is essential for efficient environmental monitoring of persistent organic pollutants. Combining analysis of PAHs, PCBs, and OCPs in a single run reduces processing time and resource use while maintaining analytical performance.
This application note details a method to simultaneously quantify 16 PAHs, 17 PCBs, and 24 OCPs in environmental samples. By adjusting concentrations to reflect typical sample levels (PAHs at 1 µg/mL; PCBs and OCPs at 0.1 µg/mL), the study evaluates the method’s throughput, resolution, and quantification accuracy within a single 32-minute run.
The approach utilizes an Agilent J&W Factor Four VF-5ms column and a quadrupole mass spectrometer in selected ion monitoring (SIM) mode. Key parameters include:
The optimized method achieved baseline separation for most analytes within 32 minutes. Challenges arose for coeluting pairs:
Emerging trends include higher-resolution stationary phases, faster temperature programs, integration with high-resolution mass spectrometry, and automated sample preparation workflows. Such advances will further streamline multi-residue analysis for regulatory monitoring and research.
The described GC–MS method on a VF-5ms column enables rapid, reliable separation and quantification of 57 target pollutants in a single 32-minute run. The approach balances throughput and selectivity, making it a versatile tool for environmental and regulatory laboratories.
GC/MSD, GC columns, Consumables
IndustriesEnvironmental, Food & Agriculture
ManufacturerAgilent Technologies
Summary
Importance of the Topic
Multi-residue gas chromatography–mass spectrometry (GC–MS) is essential for efficient environmental monitoring of persistent organic pollutants. Combining analysis of PAHs, PCBs, and OCPs in a single run reduces processing time and resource use while maintaining analytical performance.
Study Objectives and Overview
This application note details a method to simultaneously quantify 16 PAHs, 17 PCBs, and 24 OCPs in environmental samples. By adjusting concentrations to reflect typical sample levels (PAHs at 1 µg/mL; PCBs and OCPs at 0.1 µg/mL), the study evaluates the method’s throughput, resolution, and quantification accuracy within a single 32-minute run.
Methodology and Instrumentation
The approach utilizes an Agilent J&W Factor Four VF-5ms column and a quadrupole mass spectrometer in selected ion monitoring (SIM) mode. Key parameters include:
- Column: VF-5ms, 30 m × 0.25 mm ID, 0.25 µm film thickness
- Oven program: 60 °C (2 min) → 175 °C at 20 °C/min → 250 °C at 5 °C/min → 325 °C at 10 °C/min (5 min hold)
- Injection: 1 µL, splitless, injector ramp from 60 °C to 300 °C
- Carrier gas: Helium at 1 mL/min constant flow
- Detector: Quadrupole MS, EI source at 230 °C, transfer line at 280 °C, SIM acquisition
Main Results and Discussion
The optimized method achieved baseline separation for most analytes within 32 minutes. Challenges arose for coeluting pairs:
- PAHs: benzo[b]/benzo[k]-fluoranthene and indeno[1,2,3-cd]pyrene/dibenz[a,h]anthracene required careful monitoring of m/z differences.
- PCBs/OCPs: PCB 138/PCB 163 and p,p'-DDD/o,p'-DDT share similar mass spectra; cis/trans-heptachlor epoxide pair mandates additional m/z confirmation in SIM mode.
Benefits and Practical Applications
- Significant reduction in analysis time compared to separate runs for each compound class
- Comprehensive profiling of PAHs, PCBs, and OCPs in environmental matrices
- Enhanced laboratory throughput for routine monitoring and compliance testing
- Improved sensitivity due to low column bleed of the VF-5ms phase
Future Trends and Potential Applications
Emerging trends include higher-resolution stationary phases, faster temperature programs, integration with high-resolution mass spectrometry, and automated sample preparation workflows. Such advances will further streamline multi-residue analysis for regulatory monitoring and research.
Conclusion
The described GC–MS method on a VF-5ms column enables rapid, reliable separation and quantification of 57 target pollutants in a single 32-minute run. The approach balances throughput and selectivity, making it a versatile tool for environmental and regulatory laboratories.
References
- Anon (2005) Report of the Joint FAO/WHO Expert Committee on Food Additives, Sixty-fourth meeting, 8–17 February 2005, Rome, Italy.
- U.S. Environmental Protection Agency. Overview of PCBs as environmental contaminants.
- University of Illinois at Chicago, SPH Great Lakes Center. What are PCBs?
- Alaska Community Action on Toxics. Organochlorine Pesticide Fact Sheet.
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