Threshold ionisation mass spectrometry (TIMS); a complementary quantitative technique to conventional mass resolved mass spectrometry

• Published in: Vacuum 2014-03, Vol.101, p.416-422
• Main Authors: Davies, S., Rees, J.A., Seymour, D.L.
• Format: Article
• Language: English
• Subjects: Carbon monoxide; Deuterium; Electron energy; Gas sampling; Mass spectrometers; Mass spectrometry; Mathematical analysis; Metastable; Quadrupole mass spectrometer (QMS); Quadrupoles; Separation; Threshold ionisation mass spectrometry (TIMS); Thresholds
• ISSN: 0042-207X; 1879-2715
• DOI: 10.1016/j.vacuum.2013.06.004

The mass analysis of gas mixtures using quadrupole mass spectrometers is a well developed analytical technique which is routinely used with great success. The spectrometer's ionisation source is commonly one in which electrons from a heated filament are accelerated to around 70 eV before impacting with the gas samples. There are significant advantages, however, in being able to use other electron energies. Lower energies are particularly useful and are used in a so-called Threshold Ionisation mass spectrometry (TIMS) mode. The work described here applies the TIMS technique to a variety of problems which historically have proved to be difficult, and in some cases intractable, using the conventional mass resolved mode of mass spectrometry. The problems tackled include 4He/D2 and 3He/HD separation in nuclear fusion research, measuring trace levels of NH3 in air, and the separation of contributions from nitrogen and carbon monoxide to the QMS mass peak at m/z = 28. Finally, for measurements at higher gas pressures in the mass spectrometer, data for the production of long-lived metastable species are described. •Threshold ionisation MS (TIMS) quantitatively complements conventional MS analysis.•TIMS can quantitatively resolve challenging MS problems (e.g. NH3/OH and D2/He).•Novel high source pressure QMS to identify metastables in plasma and gas analysis.