A novel discharge source of hydronium ions for proton transfer reaction ionization: design, characterization, and performance
Article first published online: 15 FEB 2006
Copyright © 2006 John Wiley & Sons, Ltd.
Rapid Communications in Mass Spectrometry
Volume 20, Issue 6, pages 1025–1029, 30 March 2006
How to Cite
Inomata, S., Tanimoto, H., Aoki, N., Hirokawa, J. and Sadanaga, Y. (2006), A novel discharge source of hydronium ions for proton transfer reaction ionization: design, characterization, and performance. Rapid Commun. Mass Spectrom., 20: 1025–1029. doi: 10.1002/rcm.2405
- Issue published online: 15 FEB 2006
- Article first published online: 15 FEB 2006
- Manuscript Accepted: 21 JAN 2006
- Manuscript Revised: 20 JAN 2006
- Manuscript Received: 28 DEC 2005
A novel ion source based on direct current (d.c.) discharge has been developed for proton transfer reaction ionization operated at relatively high ion drift tube pressure. The shape and geometry of the ion source are designed to maximize overall ion intensity and to minimize interference from sample air. The initial performance of the technique, including speciation and intensity of reagent ions, their stability, and the impact of artifact signals, is evaluated by means of a proton transfer reaction time-of-flight mass spectrometer (PTR-TOFMS) newly built in our laboratory. Intensities of the hydronium (H3O+) ions are typically (5–7) × 105 counts for a 1-min integration time with a duty cycle of ∼1%. The fluctuations of the ion signals over a period of hours are within 4%. Although the formation of artifact ions from sample air (NO+ and O), which react with volatile organic compounds (VOCs) and subsequently cause fragmentation, is observed as background signals in addition to hydronium and mono- and di-hydrate H3O+ ions, intensities of both NO+ and O ions are only ∼0.5% of those of H3O+ ions. Using our PTR-TOFMS system at a drift tube pressure of ∼5 Torr, the detection sensitivities are significantly improved and the detection limits for propene, acetaldehyde, acetone, isoprene, benzene, toluene, and p-xylene are estimated to be at the sub-ppbv level for 1-min integration. Copyright © 2006 John Wiley & Sons, Ltd.