Determination of 2-Methylisoborneol, Geosmin and 2,4,6-Trichloroanisole in Drinking Water by Dynamic Headspace Coupled to Selectable 1D/2D GC-MS with Simultaneous Olfactory Detection
Applications | 2011 | GERSTELInstrumentation
Earthy off-flavor compounds such as 2-methylisoborneol, geosmin and 2,4,6-trichloroanisole introduce musty odors in drinking water and require highly sensitive analytical methods at ng/L levels due to their low odor thresholds.
This work presents a fully automated protocol combining dynamic headspace extraction with selectable one-dimensional/two-dimensional gas chromatography–mass spectrometry and simultaneous olfactory detection (DHS-1D/2D GC-O/MS) for trace analysis of off-flavor compounds in water samples.
The method offers solvent-free, highly sensitive extraction with minimal sample volume. Two-dimensional separation eliminates interferences and enhances quantitative reliability. Simultaneous olfactory detection provides additional confirmation of analyte identity.
Anticipated developments include integration of high-throughput online monitoring, expansion to other trace volatiles in environmental and food matrices, and further system miniaturization for routine QA/QC workflows.
DHS-1D/2D GC-O/MS constitutes a robust, fully automated platform for ultratrace analysis of off-flavor compounds in drinking water, delivering sub-ng/L sensitivity, enhanced selectivity and sensory confirmation suitable for water quality management.
GCxGC, GC/MSD, HeadSpace, Thermal desorption, GC/SQ
IndustriesEnvironmental
ManufacturerAgilent Technologies, GERSTEL
Summary
Significance of the Topic
Earthy off-flavor compounds such as 2-methylisoborneol, geosmin and 2,4,6-trichloroanisole introduce musty odors in drinking water and require highly sensitive analytical methods at ng/L levels due to their low odor thresholds.
Objectives and Study Overview
This work presents a fully automated protocol combining dynamic headspace extraction with selectable one-dimensional/two-dimensional gas chromatography–mass spectrometry and simultaneous olfactory detection (DHS-1D/2D GC-O/MS) for trace analysis of off-flavor compounds in water samples.
Methodology and Instrumentation
- Sample preparation: 10 mL of water spiked, salted with 30% NaCl and incubated at 80 °C.
- Extraction: GERSTEL DHS module with Tenax TA adsorbent trap; optimized dry purge of 600 mL N₂ to remove water.
- Thermal desorption: Integrated TDU unit and PTV inlet for transfer to GC.
- Chromatography: Dual LTM GC system using DB-Wax (1D) and DB-5 (2D) columns with heart-cutting and fast temperature programming (100 °C/min).
- Detection: Agilent 7890 GC with 5975C MSD in SIM mode (m/z 95, 108, 112, 125, 195, 197) and an olfactory detection port.
Main Results and Discussion
- Heart-cutting and fast 2D GC significantly reduced background and sharpened analyte peaks.
- Signal-to-noise ratios improved by factors of 12 for MIB, 9 for geosmin and 3 for TCA compared to 1D GC-O/MS.
- Calibration was linear over 1–100 ng/L (r² > 0.9942); LODs ranged from 0.15 to 0.22 ng/L.
- Simultaneous MS and olfaction confirmed compound identities at concentrations as low as 1 ng/L.
Benefits and Practical Applications
The method offers solvent-free, highly sensitive extraction with minimal sample volume. Two-dimensional separation eliminates interferences and enhances quantitative reliability. Simultaneous olfactory detection provides additional confirmation of analyte identity.
Future Trends and Potential Applications
Anticipated developments include integration of high-throughput online monitoring, expansion to other trace volatiles in environmental and food matrices, and further system miniaturization for routine QA/QC workflows.
Conclusion
DHS-1D/2D GC-O/MS constitutes a robust, fully automated platform for ultratrace analysis of off-flavor compounds in drinking water, delivering sub-ng/L sensitivity, enhanced selectivity and sensory confirmation suitable for water quality management.
Reference
- Benanou D., Acobas F., De Roubin M.R., David F., Sandra P., Anal Bioanal Chem, 2003, 376, 69.
- Malleret L., Bruchet A., Hennion M.-C., Anal Chem, 2001, 73, 1485.
- Karlsson S., Kaugare S., Grimvall A., Boren H., Savenhed R., Water Sci Technol, 1995, 31, 99.
- Zhang L., Hu R., Yang Z., Water Res, 2006, 40, 699.
- Nakamura S., Daishima S., Anal Chim Acta, 2005, 548, 79.
- Saito K., Okamura K., Kataoka H., J Chromatogr A, 2008, 1186, 434.
- Ochiai N., Sasamoto K., Takino M., Yamashita S., Daishima S., Heiden A., Hoffmann A., Analyst, 2001, 126, 1652.
- Nakamura S., Nakamura N., Ito S., J Sep Sci, 2001, 24, 674.
- Sasamoto K., Ochiai N., J Chromatogr A, 2010, 1217, 2903.
- Luong J., Gras R., Young G., Cortes H., Mustacich R., J Sep Sci, 2008, 31, 3385.
- Pawliszyn J., Solid Phase Microextraction Theory and Practice, Wiley-VCH, 1997, p. 137.
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