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5 ppb Volatiles in Drinking Water on Rtx®-VMS by EPA Method 524.3

Applications |  | RestekInstrumentation
GC/MSD, Purge and Trap, GC/SQ, GC columns, Consumables
Industries
Environmental
Manufacturer
Agilent Technologies, Restek, EST Analytical

Summary

Significance of the Topic


Volatile organic compounds (VOCs) in drinking water present health risks even at low concentrations. Monitoring trace levels of VOCs ensures regulatory compliance and protects public health. EPA Method 524.3 is a standardized approach for detecting a broad range of halogenated and aromatic volatiles in water. The use of the Rtx®-VMS capillary column enhances resolution of critical isomers, improving confidence in identification and quantitation.

Objectives and Study Overview


This application note demonstrates the analysis of 82 target VOCs at 5 ppb in drinking water using the Rtx®-VMS column and purge-and-trap gas chromatography–mass spectrometry (GC–MS). The goals are to evaluate chromatographic separation, assess sensitivity and reproducibility, and highlight the method’s suitability for routine environmental monitoring under EPA Method 524.3.

Methodology and Instrumentation


The workflow integrates purge-and-trap sample introduction with split injection (30:1) onto a 30 m x 0.25 mm ID, 1.40 µm Rtx®-VMS column. Helium carrier gas is delivered at 0.9 mL/min. The sample matrix comprises reagent-grade water fortified with a 524.3 internal standard/surrogate mix and calibration standards at 5 ng/mL.
  • Instrument: Encon Evolution purge-and-trap concentrator coupled to Agilent 7890A GC and 5975C MS detector.
  • Trap: Vocarb 3000, desorb at 260 °C for 1 min.
  • GC oven program: 45 °C hold for 4.5 min; ramp to 100 °C at 12 °C/min; ramp to 240 °C at 25 °C/min, hold 1.32 min.
  • MS conditions: scan mode 47–300 amu, source 230 °C, quadrupole 150 °C, EI 70 eV, solvent delay 1.5 min.

Main Results and Discussion


Chromatograms show baseline separation of critical compound pairs, including o-xylene and styrene, cis- and trans-isomers, and chlorobenzene isotopologues. Peak shapes are sharp and symmetric across the retention window of 2–14 minutes. Signal-to-noise ratios exceeded 100:1 for most analytes at 5 ppb. Retention time repeatability was within 0.05 minutes, and quantitation accuracy met EPA Method 524.3 criteria (±15%).

Practical Benefits and Applications


This method offers:
  • High throughput: complete run in under 15 minutes.
  • Robust isomer resolution on Rtx®-VMS column.
  • Sensitivity down to low-ppb levels for regulatory compliance.
  • Wide target range covering halogenated and aromatic VOCs.

Suitable for environmental laboratories, water utilities, and QA/QC operations focused on routine drinking water analysis.

Future Trends and Potential Applications


Advances in column technology and high-resolution MS could further lower detection limits and improve identification of emerging contaminants. Automation of sample handling and data processing will streamline workflows. Integration with online monitoring systems and digital reporting platforms will enhance real-time water quality surveillance.

Conclusion


The Rtx®-VMS column paired with purge-and-trap GC–MS fully meets EPA Method 524.3 requirements for VOC analysis in drinking water at 5 ppb. Excellent separation, sensitivity, and reproducibility make this approach a reliable choice for laboratories committed to protecting public health.

References


Restek Corporation. EPA Method 524.3 Volatile Organic Compounds in Drinking Water on Rtx®-VMS. Application Note GC_EV1297.

Content was automatically generated from an orignal PDF document using AI and may contain inaccuracies.

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