Highly Sensitive and Specific GC-MS/MS Method for the Analysis of Boron in Drinking Water and Other Beverages
Posters | 2011 | Agilent TechnologiesInstrumentation
GC/MSD, GC/MS/MS, GC/QQQ
IndustriesEnvironmental
ManufacturerAgilent Technologies
Summary
Importance of the Topic
Boron is a trace element crucial for bone health and plant growth, yet excessive exposure can adversely affect development and reproduction. Accurate quantification of boron in drinking water and beverages is essential for regulatory compliance and public health.Objectives and Study Overview
This study describes a highly sensitive and selective gas chromatography–tandem mass spectrometry (GC-MS/MS) method for measuring boron in drinking water and complex beverage matrices. The approach leverages derivatization, advanced inlet technology, and multiple reaction monitoring (MRM) to achieve low detection limits and robust matrix tolerance.Methodology and Instrumentation
- Derivatization: Boric acid is reacted with triethanolamine (0.5% w/v in acetonitrile) at 50 °C for one hour, then dried and reconstituted in ethyl acetate.
- Gas Chromatography: Agilent 7890A GC equipped with an HP-5ms column (15 m × 0.25 mm × 0.25 μm), temperature ramp from 100 °C to 280 °C at 35 °C/min.
- Injection System: Multi-Mode Inlet (MMI) operated in pulsed splitless cold-injection mode, 1 μL injection volume, ultimate-union backflush to remove high-boiling matrix compounds.
- Mass Spectrometry: Agilent 7000B triple quadrupole, electron ionization at 260 °C, MRM transitions 126→98 and 126→86 with optimized collision energies for high selectivity.
Main Results and Discussion
The method achieved a limit of detection of 2 ppb and a limit of quantitation of 15 ppb in a tomato-based vegetable matrix, significantly outperforming GC-MS SIM (80 ppb LOQ) and ICP-OES (150 ppb LOQ). Backflush dramatically reduced matrix carryover and preserved column longevity, while cold splitless injection enhanced signal-to-noise ratios. The targeted MRM transitions eliminated isobaric interferences in challenging samples.Benefits and Practical Applications
The protocol offers enhanced sensitivity and specificity for boron analysis in water and beverages, improved matrix tolerance via backflush and MS/MS discrimination, and reduced instrument maintenance through minimized contamination.Future Trends and Potential Applications
Future developments may include automated derivatization, application to soil and plant extracts, exploration of alternative derivatizing agents to further lower detection limits, and integration with online sampling for real-time environmental monitoring.Conclusion
This GC-MS/MS method delivers a rapid, robust, and highly selective tool for quantifying boron at part-per-billion levels in complex matrices, supporting regulatory compliance and quality control in water and beverage analysis.References
- Brown P, Hu H. Mechanism of boron toxicity in crop plants. 2010.
- Parks JL, Edwards M. Boron in the Environment. Crit Rev Env Sci Technol. 2005;35:81–114.
- Zeng LM, Wang HY, Guo YL. Fast quantitative analysis of boric acid by gas chromatography-mass spectrometry coupled with a simple and selective derivatization reaction using triethanolamine. J Am Soc Mass Spectrom. 2010;21(3).
- Sabarudin A, Oshita K, Oshima M. Synthesis of cross-linked chitosan possessing N-methyl-d-glucamine moiety for adsorption/concentration of boron in water samples and its accurate measurement by ICP-MS and ICP-OES. Talanta. 2005;66:136–144.
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