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Solvent-Free Extraction Technique for Determination of Semi-Volatile Organic Compounds in Water Samples by EPA Method 8270

Applications | 2018 | ENTECHInstrumentation
GC/MSD, HeadSpace, Thermal desorption, GC/SQ
Industries
Environmental
Manufacturer
Agilent Technologies, ENTECH

Summary

Significance of the Topic


Water contamination by semi-volatile organic compounds (SVOCs) poses serious health and environmental concerns. The drive to detect trace SVOCs at sub-ppb levels with minimal solvent use has led to innovations in sample preparation. Solvent-free, automated extraction methods can improve sensitivity, reduce matrix interferences, and streamline laboratory workflows in compliance with EPA Method 8270.

Objectives and Overview of the Study


This work presents a combined Vacuum Assisted Sorbent Extraction (VASE) and Pulsed Vacuum Assisted Sorbent Extraction (Pulsed VASE) approach for extracting pesticides, cannabinoids, and polycyclic aromatic hydrocarbons (PAHs) from water samples. The goal is to achieve exhaustive SVOC recovery from 1–5 mL water in a fully automated, solvent-free process, paired with GC-MS analysis for quantitative, reproducible results.

Methodology


The extraction workflow comprises:
  • VASE: In-vial vacuum extraction using a 70 mg Sorbent Pen to capture GC-compatible compounds followed by direct thermal desorption into the GC.
  • Pulsed VASE: Cyclic heating (bottom at ~100 °C, top at 50–60 °C) and cooling (~30 °C bottom) under vacuum to promote evaporation–condensation agitation that maximizes headspace transfer of low-volatility SVOCs onto the adsorbent.

Instrumentation


The analytical system includes:
  • Entech 5800 Sorbent Pen Desorption Unit (SPDU) with dual-column, split/splitless injection capability.
  • Entech Sample Preparation Rail (SPR) autosampler for automated Sorbent Pen handling.
  • Agilent 7890B GC coupled to a 5977 MS detector, operated in full-scan (33–450 m/z) with Helium carrier gas (1.5 mL/min) and a GC oven program from 40 °C to 310 °C.

Main Results and Discussion


Calibration curves for pesticides, Δ9-THC, and PAHs displayed excellent linearity down to sub-ppb levels. Independent Sorbent Pens yielded consistent response factors, demonstrating low carryover and high reproducibility. Pulsed VASE accelerated extraction kinetics compared to static headspace, enabling quantitative recoveries from just 1 mL water—comparable to traditional solvent extraction of 1 L samples but without solvent cleanup.

Benefits and Practical Applications


This method offers:
  • Solvent-free extraction, reducing environmental impact and operational costs.
  • Broad SVOC range coverage without matrix contact artifacts.
  • Fast, automated workflows suitable for routine water quality monitoring and EPA 8270 compliance.
  • Reduced sample volumes and simplified sample preparation.

Future Trends and Potential Applications


Future developments include application to complex matrices (soil, biological fluids), integration with tandem MS for enhanced selectivity, and validation with field water samples. High-throughput autosampler integration will further improve laboratory efficiency and lower detection limits.

Conclusion


The combined VASE/Pulsed VASE workflow delivers a robust, reproducible, and efficient solvent-free extraction of SVOCs in water. It meets trace-level detection requirements, simplifies sample preparation, and supports regulatory compliance under EPA Method 8270.

Reference


Cardin D.B.; Noad V.L. Solvent-Free Extraction Technique for Determination of Semi-Volatile Organic Compounds in Water Samples by EPA Method 8270. Entech Instruments Application Note V-3742-01, 2018.

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