Interlaboratory comparison of limits of detectic in negative chemical ionization mass spectrometry

Data are presented on the limits of detection for a series of nine compounds in negative chemical ionization (NCI) mass spectra obtained in five different mass spectrometers: Finnigan 4000 with a 4500 ion source, Kratos MS-80, Hewlett-Packard 5985 and two Finnigan 4500s. The nine compounds undergo either resonance capture or dissociative capture of an electron at optimum energies ranging from 0.0 to 1.1 eV. The limits of detection generally increased with increasing optimum electron energy. The limit of detection as a function of optimum electron capture energy is expected to provide information about the electron energy distribution in the ion source. The data showed scatter within and between instruments. The scatter is believed to the due primarily to reactions with low levels of adventitious gases such as oxygen in the ion source. The data also suggested wide variations in electron energies between the instruments. The variation in the electron energy distribution is thought to have been caused by variations in the ion optical fields within the instruments. The results suggest that the requirements for reproducibility in NCI mass spectra at the limit of detection are rigorous control of trace gases in the ion source, control of the electric fields within the source including ion optical fields that penetrate the source aperture and control of pressure, temperature and other factors that influence NCI mass spectra

[1]  R. Hites,et al.  A systematic study of instrumental parameters affecting electron capture negative ion mass spectra , 1988 .

[2]  R. Hites,et al.  Electron capture negative ion mass spectra of halogenated diphenylethane derivatives , 1988 .

[3]  M. Deinzer,et al.  Interlaboratory comparison of methane electron capture negative ion mass spectra. , 1988, Analytical chemistry.

[4]  M. Oehme,et al.  Comparison of the reproducibility of negative ion chemical ionization mass spectra obtained by different reagent gases on two commercial quadrupole instruments , 1986 .

[5]  D. Stöckl,et al.  Negative chemical ionization spectra of aromatic acids and esters or are negative chemical ionization spectra of use only if one knows what one is looking for , 1982 .

[6]  G. Alton Aspects of the physics, chemistry, and technology of high intensity heavy ion sources , 1981 .

[7]  H. Budzikiewicz Mass Spectrometry of Negative Ions , 1981 .

[8]  L. Christophorou Negative ions of polyatomic molecules. , 1980, Environmental health perspectives.

[9]  L. Christophorou,et al.  Fragmentation of aliphatic chlorocarbons under low‐energy (≲10 eV) electron impact , 1977 .

[10]  T. S. Green Intense ion beams , 1974 .

[11]  L. Christophorou,et al.  Electron attachment and ‘carrier gas’ energy distribution functions☆ , 1969 .

[12]  L. Christophorou,et al.  Electron Attachment to Halogenated Aliphatic Hydrocarbons , 1968 .

[13]  G. S. Hurst,et al.  Dissociative Electron Capture by Benzene Derivatives , 1966 .

[14]  E. W. McDaniel,et al.  Collision phenomena in ionized gases , 1964 .