A new gas chromatography/mass spectrometry (GC/MS) system was designed and
evaluated which we have named 'Supersonic GC/MS'. It is based on a modifica
tion of a commercially available GC/MS system to include a supersonic molec
ular beam (SMB) MS interface. In this system the standard electron ionizati
on (EI) ion source was replaced with a fly-through EI ion source mounted in
the path of the SMB. A hyperthermal surface ionization (HSI) ion source co
mbined with a 90 degrees ion mirror (for the EI-produced ions) was also add
ed, and placed inside the quadrupole mass analyzer in place of its original
EI ion source. The 'Supersonic GC/MS' system requires 18 cm added bench sp
ace plus the addition of an air-cooled 60 L/s diffusion pump and a 537 L/mi
n rotary pump. The system is user friendly since all the gas flow rates, he
ated zones, sampling and data analysis are performed the same way as the or
iginal system and are computer-controlled via the original software. Simila
r EI sensitivity was obtained as with the original system for hexachloroben
zene and octafluoronaphthalene, while improved EI detection limits were dem
onstrated for methyl stearate and eicosane due to the significant enhanceme
nt of their molecular ion abundances. A GC/MS detection limit of 500 ag for
pyrene was demonstrated using HSI. Good supersonic expansion cooling was a
chieved with large alkanes, despite the use of a rotary pump at the nozzle
chamber instead of a diffusion pump. High temperature GC/MS analysis was de
monstrated for large polycyclic aromatic hydrocarbons (PAHs) including oval
ene and decacyclene (ten rings). Library searches with EI mass spectra are
demonstrated, and it is explained why the enhancement of the molecular ion
actually improves the library search in most cases. The analysis of large p
hthalate esters is also described, and the improvement obtained is shown to
originate from their enhanced molecular and high mass fragment ions. Copyr
ight (C) 2001 John Wiley & Sons, Ltd.