Binocular method and apparatus for stoichiometric analysis and imaging using subatomic particle activation

• US 20050195931A1
• Filed: 03/21/2005
• Published: 09/08/2005
• Est. Priority Date: 02/18/1998
• Status: Abandoned Application

• Current Assignee: Bioatom, Calsec California Science & Engineering Corporation, Clear Path Technologies Incorporated, Hiet Acquisition, LLC
• Original Assignee: Calsec California Science & Engineering Corporation
• Inventors: Maglich, Bogdan C.
• Application Number:
  US11/084,963
• Publication Number:
  US 20050195931A1
• Time in Patent Office: Days
• US Class Current: 376/156
• CPC Class Codes: G01N 23/222 using neutron activation analysis [NAA]

Abstract

An apparatus and method for detecting, locating, and analyzing chemical compounds located within a test subject using subatomic particle activation. In a first embodiment, an excitation source excites a target to simultaneously produce beams each consisting of certain subatomic species, for example fast neutrons and alpha particles. The test subject (and chemical compounds contained therein) is irradiated by the fast neutrons, thereby stimulating the emission of prompt gamma rays. Gamma and alpha detectors are positioned relative to the test subject and target(s) so as to detect the emitted prompt gamma rays and alpha particles in substantial coincidence, and the known physical relationship between the beams is used to spatially locate the activated chemical compound. Energy spectra derived from the gamma detectors are filtered to eliminate all non-relevant spectral artifacts, thereby 1) permitting the creation of a plurality of parallel coincidence channels; 2) reducing the subsequent signal processing required; and 3) increasing the overall accuracy and efficiency of the chemical compound identification and analysis processes. In a second embodiment, thermal neutron-induced gamma emissions are detected and analyzed in conjunction with the fast neutron-induced gammas to provide a warning signal of the possible presence of certain types of contraband. A multi-beam/multi-target embodiment is also disclosed for more accurate spatial location. A method for calibrating and evaluating the efficacy of the system under varying test parameters is further disclosed.

Claims

1. A method of providing non-invasive, stoichiometric analysis and imaging of a substance comprising atomic nuclei which emit one or more gamma rays having energies characteristic of the atomic nuclei in response to neutron irradiation, the method comprising:

emitting a first plurality of neutron/alpha particle pairs from a first location separate from the substance, each pair comprising a neutron having an energy of approximately 14 MeV and a corresponding alpha particle, the neutron and the alpha particle generated by the same nuclear reaction, the neutron and the alpha particle propagating in substantially opposite directions;

detecting alpha particles from the first location propagating generally within a first solid angle with respect to the first location away from the substance, the first solid angle generally centered along a first line;

irradiating a region of the substance with neutrons from the first location propagating generally within the first solid angle toward the substance, the region emitting gamma rays in response thereto;

emitting a second plurality of neutron/alpha particle pairs from a second location separate from the substance, each pair comprising a neutron having an energy of approximately 14 MeV and a corresponding alpha particle, the neutron and the alpha particle generated by the same nuclear reaction, the neutron and the alpha particle propagating in substantially opposite directions, the second location spaced from the first location;

detecting alpha particles from the second location propagating generally within a second solid angle with respect to the second location away from the substance, the second solid angle generally centered along a second line different from the first line;

irradiating the region of the substance with neutrons from the second location propagating generally within the second solid angle toward the substance, the region emitting gamma rays in response thereto;

detecting at least a portion of the gamma rays emitted by the substance in response to being irradiated by the neutrons from the first location and by the neutrons from the second location, and generating a plurality of gamma detection signals in response thereto;

energy-filtering the plurality of gamma detection signals to generate a plurality of energy-filtered gamma signals by passing gamma detection signals corresponding to detected gamma rays having energies characteristic of the atomic nuclei of the substance and by rejecting gamma detection signals corresponding to detected gamma rays having energies which are not characteristic of the atomic nuclei of the substance;

detecting coincidences between the energy-filtered gamma signals and the detected alpha particles from the first location; and

detecting coincidences between the energy-filtered gamma signals and the detected alpha particles from the second location.

2. The method of claim 1, further comprising triangulating a position of the region by determining an intersection of the first solid angle and the second solid angle.

3. The method of claim 1, wherein detecting at least a portion of the gamma rays comprises using a solid-state photon detector having an energy resolution less than or equal to approximately 0.5%.

4. The method of claim 3, wherein detecting at least a portion of the gamma rays comprises using a solid-state photon detector having an energy resolution of approximately 0.1%.

5. The method of claim 1, wherein the detected gamma rays have energies between 1.6 MeV and 7.2 MeV.

6. The method of claim 1, wherein the first line and the second line have a nonzero angle therebetween.

7. The method of claim 1, wherein emitting the first plurality of neutron/alpha particle pairs comprises irradiating a first target comprising tritium nuclei with a first plurality of deuterium nuclei, and wherein emitting the second plurality of neutron/alpha particle pairs comprises irradiating a second target comprising tritium nuclei with a second plurality of deuterium nuclei.

8. The method of claim 7, wherein the first plurality of deuterium nuclei and the second plurality of deuterium nuclei are emitted by a charged-particle accelerator.

9. The method of claim 7, wherein the first plurality of deuterium nuclei are emitted by a first charged-particle accelerator and the second plurality of deuterium nuclei are emitted by a second charged-particle accelerator.

10. The method of claim 1, wherein the alpha particles from the first location are detected by a first array of alpha particle detectors and the alpha particles from the second location are detected by a second array of alpha particle detectors.

11. The method of claim 1, wherein the region is irradiated by neutrons from the first location and by neutrons from the second location simultaneously.

12. The method of claim 1, further comprising calculating stoichiometric atomic ratios of atomic nuclei of the substance and identifying the substance using the calculated stoichiometric atomic ratios.

13. The method of claim 12, wherein stoichiometric atomic ratios of carbon-to-nitrogen, carbon-to-oxygen, and nitrogen-to-oxygen are used to identify the substance by its empirical chemical formula.

14. The method of claim 1, wherein the substance comprises a nitrogen-containing explosive material, and the energy-filtered gamma signals comprise gamma detection signals corresponding to detected gamma rays having energies which are characteristic of nitrogen nuclei.

15. The method of claim 1, wherein detecting coincidences between the energy-filtered gamma signals and the detected alpha particles from the first location is performed to within 1 to 100 nanoseconds.

16. The method of claim 1, wherein detecting coincidences between the energy-filtered gamma signals and the detected alpha particles from the second location is performed to within 1 to 100 nanoseconds.

17. A method of providing non-invasive, stoichiometric analysis and imaging of a substance comprising atomic nuclei which emit one or more gamma rays having energies characteristic of the atomic nuclei in response to neutron irradiation, the method comprising:

emitting neutron/alpha particle pairs from a first location separate from the substance and from a second location separate from the substance, the second location spaced from the first location, each pair comprising a neutron and a corresponding alpha particle propagating in substantially opposite directions;

detecting alpha particles from the first location propagating generally within a first solid angle with respect to the first location away from the substance and alpha particles from the second location propagating generally within a second solid angle with respect to the second location away from the substance, the first solid angle generally centered along a first line, the second solid angle generally centered along a second line different from the first line;

irradiating a region of the substance with neutrons from the first location propagating generally within the first solid angle toward the substance and with neutrons from the second location propagating generally within the second solid angle toward the substance, the region emitting gamma rays in response thereto; and

detecting at least a portion of the gamma rays emitted by the substance in response to being irradiated by the neutrons from the first location and by the neutrons from the second location.

18. The method of claim 17, wherein the gamma rays are detected by an n-type solid-state gamma ray detector, the method further comprising:

generating a plurality of gamma detection pulses in response to the detected gamma rays;

selecting at least one energy characteristic of the atomic nuclei of the substance;

energy-filtering the plurality of gamma detection pulses to generate a plurality of energy-filtered gamma pulses by passing gamma detection pulses corresponding to detected gamma rays having the at least one selected energy characteristic of the atomic nuclei of the substance and by rejecting gamma detection pulses corresponding to detected gamma rays not having the at least one energy characteristic of the atomic nuclei of the substance; and

detecting coincidences between the energy-filtered gamma pulses and the detected alpha particles from the first location and between the energy-filtered gamma pulses and the detected alpha particles from the second location.

19. The method of claim 17, wherein the neutrons irradiating the region have a kinetic energy of approximately 14 MeV.

20. A method of providing non-invasive, stoichiometric analysis and imaging of a substance comprising atomic nuclei which emit one or more gamma rays having energies characteristic of the atomic nuclei in response to neutron irradiation, the method comprising:

emitting neutron/alpha particle pairs from a plurality of locations spaced from the substance and from one another, each pair comprising a neutron and a corresponding alpha particle propagating in substantially opposite directions;

detecting alpha particles from the plurality of locations propagating away from the substance;

irradiating a region of the substance with neutrons from the plurality of locations propagating toward the substance, the neutrons corresponding to the detected alpha particles, the region emitting gamma rays in response thereto; and

detecting at least a portion of the gamma rays emitted by the substance in response to being irradiated by the neutrons from the first location and by the neutrons from the second location.

21. The method of claim 20, wherein the gamma rays are detected by a solid-state gamma ray detector, the method further comprising:

generating a plurality of gamma detection signals in response to the detected gamma rays detected by the solid-state gamma ray detector, each gamma detection signal indicative of the energy of the corresponding detected gamma ray;

filtering the plurality of gamma detection signals by gamma ray energy to generate a plurality of filtered signals by passing gamma detection signals corresponding to detected gamma rays having energies characteristic of the atomic nuclei of the substance and by rejecting gamma detection signals corresponding to detected gamma rays having energies which are not characteristic of the atomic nuclei of the substance; and

detecting coincidences between the filtered signals and the detected alpha particles from the plurality of locations.

22. The method of claim 21, wherein detecting coincidences between the filtered signals and the detected alpha particles is performed to within 1 to 100 nanoseconds.