Method 8260C by Purge and Trap Gas Chromatography Mass Spectrometry using the Clarus SQ 8
Applications | 2012 | PerkinElmerInstrumentation
Volatile organic compounds (VOCs) are common environmental contaminants that pose risks to human health and ecosystems. Sensitive and reproducible analytical methods are essential for monitoring VOC levels in water, soil, air, and other matrices to ensure regulatory compliance and public safety.
This study evaluates the performance of the PerkinElmer Clarus SQ 8 GC/MS system with a purge and trap sample introduction in accordance with U.S. EPA Method 8260C. The aim is to demonstrate that the system meets or exceeds the method criteria for detection limits, calibration linearity, precision, and accuracy across a wide concentration range.
Gas chromatograph: PerkinElmer Clarus 680 GC with Elite 624 MS capillary column (30 m × 0.25 mm × 1.4 μm)
Mass spectrometer: PerkinElmer Clarus SQ 8C in electron ionization full-scan mode (m/z 35–270)
Sample introduction: Teledyne Tekmar Atomx purge and trap system with Tekmar #9 trap
Samples of 5 mL were purged at 40 °C for 11 minutes using 40 mL/min flow, followed by dry purge and thermal desorption at 200 °C. The GC oven ramped from 40 °C to 200 °C at programmed rates to achieve efficient separation within a short runtime. The MS transfer line and ion source were maintained at 220 °C and 300 °C, respectively. Calibration standards covered nine levels from 0.5 to 200 μg/L, with surrogate and internal standards added at 20 μg/L to ensure quantitation accuracy.
Calibration curves for most VOCs showed linearity with R2 values above 0.990. Method detection limits were below 0.5 μg/L for the majority of analytes. Precision experiments yielded relative standard deviations below 5%, and recovery studies fell within 85–115%. The fast cooling dual-walled GC oven enabled an injection-to-injection cycle under 30 minutes, maximizing sample throughput. Optimized detector voltage settings allowed full-scan detection at trace levels without saturation at higher concentrations.
Emerging acquisition modes such as selected ion full ion (SIFI) and selected ion monitoring (SIM) will further enhance sensitivity for targeted compounds. Integration of automated sample preparation, advanced data processing, and larger spectral libraries will expand applications in environmental monitoring, industrial quality control, and forensic investigations.
The PerkinElmer Clarus SQ 8 GC/MS system with purge and trap sample introduction meets and exceeds EPA Method 8260C requirements, offering reliable, high-throughput analysis of VOCs with excellent sensitivity, precision, and accuracy.
GC/MSD, Purge and Trap, GC/SQ
IndustriesEnvironmental
ManufacturerPerkinElmer
Summary
Importance of the Topic
Volatile organic compounds (VOCs) are common environmental contaminants that pose risks to human health and ecosystems. Sensitive and reproducible analytical methods are essential for monitoring VOC levels in water, soil, air, and other matrices to ensure regulatory compliance and public safety.
Objectives and Study Overview
This study evaluates the performance of the PerkinElmer Clarus SQ 8 GC/MS system with a purge and trap sample introduction in accordance with U.S. EPA Method 8260C. The aim is to demonstrate that the system meets or exceeds the method criteria for detection limits, calibration linearity, precision, and accuracy across a wide concentration range.
Instrumentation Used
Gas chromatograph: PerkinElmer Clarus 680 GC with Elite 624 MS capillary column (30 m × 0.25 mm × 1.4 μm)
Mass spectrometer: PerkinElmer Clarus SQ 8C in electron ionization full-scan mode (m/z 35–270)
Sample introduction: Teledyne Tekmar Atomx purge and trap system with Tekmar #9 trap
Methodology and Instrumentation
Samples of 5 mL were purged at 40 °C for 11 minutes using 40 mL/min flow, followed by dry purge and thermal desorption at 200 °C. The GC oven ramped from 40 °C to 200 °C at programmed rates to achieve efficient separation within a short runtime. The MS transfer line and ion source were maintained at 220 °C and 300 °C, respectively. Calibration standards covered nine levels from 0.5 to 200 μg/L, with surrogate and internal standards added at 20 μg/L to ensure quantitation accuracy.
Key Results and Discussion
Calibration curves for most VOCs showed linearity with R2 values above 0.990. Method detection limits were below 0.5 μg/L for the majority of analytes. Precision experiments yielded relative standard deviations below 5%, and recovery studies fell within 85–115%. The fast cooling dual-walled GC oven enabled an injection-to-injection cycle under 30 minutes, maximizing sample throughput. Optimized detector voltage settings allowed full-scan detection at trace levels without saturation at higher concentrations.
Benefits and Practical Applications
- Full-scan acquisition provides library-searchable spectra even at low concentration levels
- Wide dynamic range (0.5–200 μg/L) allows analysis of trace and elevated VOCs without retuning
- Rapid GC cooling and automated purge and trap enhance laboratory throughput
- Demonstrated precision and accuracy support regulatory compliance in environmental testing
Future Trends and Applications
Emerging acquisition modes such as selected ion full ion (SIFI) and selected ion monitoring (SIM) will further enhance sensitivity for targeted compounds. Integration of automated sample preparation, advanced data processing, and larger spectral libraries will expand applications in environmental monitoring, industrial quality control, and forensic investigations.
Conclusion
The PerkinElmer Clarus SQ 8 GC/MS system with purge and trap sample introduction meets and exceeds EPA Method 8260C requirements, offering reliable, high-throughput analysis of VOCs with excellent sensitivity, precision, and accuracy.
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