Rapid response mass spectrometer system

Radiant energy – Ionic separation or analysis – Ion beam pulsing means with detector synchronizing means

Reexamination Certificate

Rate now

  [ 0.00 ] – not rated yet Voters 0   Comments 0

Details

C250S288000, C250S292000, C250S42300F

Reexamination Certificate

active

06326615

ABSTRACT:

BACKGROUND OF THE INVENTION
1. Field of the Invention
The present invention relates to a mass spectrometer which has a glow discharge ionizer and a photoionizer that are coupled to a mass detector(s) by quadrupole ion traps.
2. Background Information
Terrorists have been known to use explosives to hijack commercial aircraft. For this reason, there has been a desire to provide an explosive detection system that can be operated “on-site” at an airport terminal. An on-site detection system must be capable of detecting extremely low concentrations of an explosive(s) material in a relatively fast time frame to minimize the time delays in air travel for the passengers.
U.S. Pat. No. 5,854,431 issued to Linker et al. and assigned to Sandia Corporation (“Sandia”) discloses a preconcentrator system that generates a flow of air to dislodge explosive material from a passenger. The dislodged explosive material is captured by a screen of the system. The air flow across the passenger is temporarily terminated to allow the captured explosive material to be removed from the screen by a secondary flow of air. The explosive material removed from the screen is directed into a particle detector. The preconcentrator disclosed in the Sandia patent increases the concentration of explosive material provided to the detector.
U.S. Pat. No. 4,849,628 issued to McLuckey et al. (“McLuckey”) discloses a mass detection system that can detect relatively low concentrations of a trace molecule(s). McLuckey utilizes a glow discharge ionizer which ionizes an “atmospheric” sample. Providing an air sample at atmospheric pressures increases the density of the sample and the number of ionized molecules. Increasing the number of ions improves the sensitivity of the detector.
The glow discharge ionizer includes a pair of electrodes separated by a chamber. A voltage potential is created between the electrodes to induce a glow discharge which ionizes a gas sample within the chamber. The glow discharge ionizer of McLuckey is coupled to a quadrupole mass spectrometer that can detect a trace molecule such as an explosive material.
The quadrupole mass spectrometer includes a scanning circuit which provides a continuously varying voltage field across the poles of the spectrometer. The continuously varying voltage field sequentially ejects ionized molecules from the quadrupole to a detector. The excitation circuit and detector can be coupled to a computer which correlates detected molecules with the excitation voltage. Explosive materials will provide detection at a predetermined voltage(s). The computer can correlate detection with an explosive material and inform an operator that an explosive has been detected.
Quadrupole mass spectrometers are relatively slow because of the time required to vary the excitation voltage to sequentially eject the ionized trace molecules. The prior art does include time of flight mass spectrometers, which simultaneously accelerate all of the ionized molecules toward a detector and then detect the different times when the molecules arrive. The mass of the molecules varies with the different arrival times. Time of flight mass spectrometers are not effective when used with a continuous ionization source such as a glow discharge ionizer. It would be desirable to provide a monitor that can quickly detect trace molecules in relatively low concentrations.
Glow discharge ionizers are efficient in ionizing molecules with high electron affinity but are not generally effective for molecules with low ionization potentials, which generally have low electron affinity. It would also be desirable to provide a monitor that can quickly detect a variety of different trace molecules in relatively low concentrations. For example, it would be desirable to provide an on-site airport terminal detector that can detect explosives as well as other threats and contraband such as chemical weapons and drugs.
SUMMARY OF THE INVENTION
The present invention includes an embodiment of a monitor for detecting a trace molecule from a gas sample. The monitor may include a glow discharge ionizer and a threshold photoionizer, which can ionize a trace molecule from the gas sample. The ionized trace molecule is trapped within a quadrupole ion trap. The quadrupole ion trap is coupled to a mass detector which can detect the ionized trace molecule.


REFERENCES:
patent: 4365157 (1982-12-01), Unsold et al.
patent: 4540884 (1985-09-01), Stafford et al.
patent: 4733073 (1988-03-01), Becker et al.
patent: 4780608 (1988-10-01), Cross et al.
patent: 4849628 (1989-07-01), McLuckey et al.
patent: 4861988 (1989-08-01), Henion et al.
patent: 4931640 (1990-06-01), Marshall et al.
patent: 5070240 (1991-12-01), Lee et al.
patent: 5206594 (1993-04-01), Zipf
patent: 5283436 (1994-02-01), Wang
patent: 5393979 (1995-02-01), Hsi
patent: 5397895 (1995-03-01), Leone et al.
patent: 5504328 (1996-04-01), Bonser
patent: 5554846 (1996-09-01), Regiee et al.
patent: 5569917 (1996-10-01), Buttrill, Jr. et al.
patent: 5631462 (1997-05-01), Reents, Jr.
patent: 5808299 (1998-09-01), Syage
patent: 5854431 (1998-12-01), Linker et al.
patent: 5869832 (1999-05-01), Kang et al.
patent: 6011259 (2000-01-01), Whitehouse et al.
patent: 6040575 (2000-03-01), Whitehouse et al.
patent: 6140638 (2000-10-01), Tanner et al.
Mahon, McIlrath, Myerscough, Koopman, Third-Harmonic Generation in Argon, Krypton, and Xenon: Bandwidth Limitations in the Vicinity of Lyman-&agr;, 1979, Eight (8) pages, vol. QE-15, IEEE.
R. Wallenstein, Generation of Narrowband Tunable VUV Radiation at the Lyman -&agr; Wavelength, Apr. 1980, Four (4) pages, vol. 33 No. 1, Optics Communication, West Germany.
R. Hilbig and R. Wallenstein, Tunable VUV Radiation Generated by Two-Photon Resonant Frequency Mixing in Xenon, Feb. 1983, vol. QE-19, IEEE.
C. Rettner, E. Marinero, R. Zare, A. Kung, Pulsed Free Jets: Novel Nonlinear Media for Generation of Vacuum Ultrviolet and Extreme Ultrviolet Radiation, 1984, Seven (7) pages, American Chemical Society.
Roger Tembreull and David M. Lubman, Pulsed Laser Desorption of Biological Molecules in Supersonic Beam Mass Spectrometry with Resonant Two-Photon Ionization Detection, Apr. 15, 1987, Seven (7) pages, Analytical Chemistry, vol. 59, No. 8, Michigan.
E.R. Rohwer, R.C. Beavis, C. Koster, J. Lindner, J. Grotemeyer and E.W. Schlag, Fast Pulsed Laser Induced Electron Generation for Electron Impact Mass Spectrometry, Nov. 23, 1988.
Russell G. Tonkyn and Michael G. White, Compact Vacuum Ultrviolet Source for Photoelectron Spectroscopy, Mar. 20, 1989, Seven (7) pages, American Institute of Physics.
J.G. Boyle, L.D. Pfefferle, E.E. Gulcicek, S.D. Colson, Laser-driven Electron Ionization for a VUV Photoionization Time-of-Flight Mass Spectrometer, Oct. 1990, Eleven (11) pages, American Institute of Physics.
David M. Lubman, Lasers and Mass Spectrometry, 1990, Twelve (12) pages, Oxford University Press, New York, Oxford.
Jack A. Syage, Real-Time Detection of Chemical Ageuis Using Molecular Beam Laser Mass Spectrometry, 1990, Five (5) pages, American Chemical Society.
R. Frey, A. Holle, H. Betzold, W. Ulke, U. Boest, Real-Time Vehicle Exhaust Analysis Using a Laser TOF Mass Spectrometer, 1992, Two (2) pages.
Steven M. Michael, Mingta Chien and David M. Lubman, An Ion Trap Storage/Time-of-Flight Mass Spectrometer, Jun. 17, 1992, Four (4) pages, American Institute of Physiscs, Michigan.
P.Y.Cheng and H.L. Dai, A Photoemitted Electron-Impact Ionization Method for Time-of-Flight Mass Spectrometers, May 12, 1993, Four (4) pages, American Institute of Physics.
U. Boesl, R. Weinkauf, C. Weickhardt, E.W. Schlag, Laser Ion Sources for Time-of-Flight Mass Spectrometry, Thirty-Eight (38) pages, Sep. 14, 1993.
Dale R. Nesselrodt and Tomas Baer, Cyclic Ketone Mixture Analysis Using 2+1 Resonance-Enhanced Multiphoton Ionization Mass Spectrometry, Aug. 1, 1994, Eight (8) pages, vol. 66, No. 15, Analytical Chemistry.
Mark G. Qian and David M. Lubman, A Marriage made in MS, Apr. 1, 1995, Four (4) pages, vol. 67, No. 7, Analytical Chemistry.

LandOfFree

Say what you really think

Search LandOfFree.com for the USA inventors and patents. Rate them and share your experience with other people.

Rating

Rapid response mass spectrometer system does not yet have a rating. At this time, there are no reviews or comments for this patent.

If you have personal experience with Rapid response mass spectrometer system, we encourage you to share that experience with our LandOfFree.com community. Your opinion is very important and Rapid response mass spectrometer system will most certainly appreciate the feedback.

Rate now

     

Profile ID: LFUS-PAI-O-2592771

  Search
All data on this website is collected from public sources. Our data reflects the most accurate information available at the time of publication.