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Optimizing the Analysis of Semi-volatiles by EPA Method 8270

Applications | 2016 | Thermo Fisher ScientificInstrumentation
GC/MSD, GC/SQ
Industries
Environmental
Manufacturer
Thermo Fisher Scientific

Summary

Importance of the topic


The analysis of semi-volatile organic compounds (SVOCs) in environmental samples is critical for assessing pollution levels in soils, waste matrices, water and air sampling media. EPA Method 8270D remains a cornerstone for routine monitoring in environmental and industrial laboratories. Optimizing GC-MS performance ensures reliable detection over a wide concentration range while controlling operational costs.

Objectives and overview of the study


This study evaluated the Thermo Scientific ISQ Series single-quadrupole GC-MS system for compliance with U.S. EPA Method 8270D. Specific goals included:
  • Verifying instrument tuning using DFTPP ion abundance criteria.
  • Establishing calibration linearity from 0.2 to 200 ppm with a single column.
  • Assessing the impact of the Instant Connect Helium Saver Module on helium consumption and analytical performance.

Methodology and instrumentation


System setup and sample preparation followed EPA Method 8270D guidelines:
  • DFTPP tuning mix was injected to meet ion abundance specifications via TraceFinder and Chromeleon software.
  • Calibration standards (0.2–50 ppm splitless and 2–200 ppm split) with six surrogates were prepared in methylene chloride and spiked with internal standards at 5 ppm.
  • Both splitless and split injection modes were evaluated using the same column and liner to simplify workflows.
  • The Instant Connect Helium Saver Module diverted septum purge and split flows to nitrogen, reducing helium usage while maintaining carrier gas purity for the analytical column.

Results and discussion


Key findings demonstrated robust performance across both injection modes:
  • Over 90 % of the 76 target SVOCs achieved relative response factor (RRF) RSD < 20 % with a linear calibration fit.
  • A small subset of compounds required alternative curve fitting, in full compliance with EPA criteria for RRF and correlation coefficients (r2).
  • The Helium Saver Module reduced helium consumption by approximately 90 % without affecting calibration results or compound response factors.
  • The ISQ source design allowed rapid, front-access removal and cleaning of ion optics without system venting, minimizing downtime.

Benefits and practical applications


The optimized GC-MS method offers several advantages for routine environmental analysis:
  • Extended dynamic range (0.2–200 ppm) using a single column and liner reduces consumable costs and simplifies method setup.
  • Automated software reports streamline compliance checks for tune verification, calibration, internal standards and quality control.
  • Significant helium savings lower operating expenses and environmental impact.
  • Modular source design enhances laboratory uptime and flexibility for maintenance or method changes.

Future trends and potential applications


Emerging developments and opportunities include:
  • Integration of cloud-based data management and AI-driven quality control for real-time method validation.
  • Expansion of calibration strategies to cover emerging contaminants and high-throughput screening workflows.
  • Further enhancements in gas-saving technologies and alternative carrier gases for greener GC-MS operation.

Conclusion


The Thermo Scientific ISQ Series single-quadrupole GC-MS system fully meets EPA Method 8270D requirements. Its extended dynamic range, automated compliance software and Helium Saver Module deliver robust SVOC analysis with reduced helium consumption and operational costs. The innovative source design ensures rapid maintenance and sustained performance, making the ISQ platform an efficient solution for environmental laboratories.

Reference


  • U.S. EPA. Method 8270D: Semivolatile Organic Compounds by GC/MS (SW-846), Revision 5, July 2014.
  • Eichelberger J.W., Harris L.E., Budde W.L. Anal. Chem. 1975, 47 (7), 995–1000.
  • Donnelly J.R. J. Assoc. Off. Anal. Chem. 1988, 71 (2), 434–439.
  • Tondeur Y., Niederhüttl W.J., Campana J.E., Mitchum R.K., Sovocool G.W., Donnelly J.R. J. Mass Spectrom. 1988, 15 (8), 429–439.

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