US2018284066A1PendingUtilityA1
System and method for trace detection using dual ionization sources
Est. expiryMar 24, 2035(~8.7 yrs left)· nominal 20-yr term from priority
G01N 33/0036G01N 27/622H01J 49/107H01J 37/08G01N 33/227
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Claims
Abstract
A dual source ionizer includes a first ionization source and a second ionization source. The first ionization source is configured to generate a first electric field. The first electric field has a first field strength that is insufficient to form NOx− ions. The second ionization source is configured to generate a second electric field. The second electric field has a second field strength that is sufficient to form ozone and the NOx− ions.
Claims
exact text as granted — not AI-modified1 . A dual source ionizer comprising:
a first ionization source configured to generate a first electric field, the first electric field having a first field strength insufficient to form NO x − ions; and a second ionization source configured to generate a second electric field, the second electric field having a second field strength sufficient to form ozone and the NO x − ions.
2 . The dual source ionizer of claim 1 further comprising a controller configured to disable said second ionization source for a period of time while said first ionization source is enabled.
3 . The dual source ionizer of claim 1 wherein said first ionization source comprises a radioactive ionization source.
4 . The dual source ionizer of claim 1 wherein the first ionization source comprises a photoionization source.
5 . The dual source ionizer of claim 1 wherein the first ionization source comprises an X-ray source.
6 . The dual source ionizer of claim 1 wherein the first field strength is no greater than 10 megavolts per meter, and wherein the first electric field is generated in a volume having a pressure of substantially 1 atmosphere.
7 . The dual source ionizer of claim 1 wherein the second ionization source comprises an electrical discharge radiation source.
8 . The dual source ionizer of claim 1 wherein the second field strength is at least 12.5 megavolts per meter, and wherein the second electric field is generated in a volume having a pressure of substantially 1atmosphere.
9 . A method of ionizing a gas, the method comprising:
ionizing the gas using a first ionization source configured to generate one of the group consisting of a low-strength electric field and no electric field; enabling a second ionization source for a duration; and ionizing the gas using the second ionization source configured to generate a high-strength electric field.
10 . The method of claim 9 , wherein ionizing the gas using the first ionization source is carried out over a scan duration that is determined according to a vaporization time of a chemical substance sample.
11 . The method of claim 9 , wherein the duration the second ionization source is enabled is a portion of the scan duration.
12 . The method of claim 9 further comprising disabling the first ionization source before enabling the second ionization source.
13 . The method of claim 9 further comprising performing spectrometry on ions of the gas to screen for a target chemical substance.
14 . The method of claim 13 , wherein performing spectrometry comprises performing mass spectrometry.
15 . The method of claim 13 , wherein performing spectrometry further comprises screening for a nitrate-based explosive and for a non-nitrate-based explosive.
16 . A trace detection system comprising:
a chamber configured to contain a gas composed of at least vapor of a chemical substance sample; a first ionization source configured to generate a low-strength electric field in said volume to ionize the gas; a second ionization source configured to generate a high-strength electric field in said volume to ionize the gas; and a switch configured to enable said second ionization source for a portion of a scan duration and to disable said second ionization source.
17 . The trace detection system of claim 16 further comprising a spectrometer configured to screen ions of the gas for a nitrate-based explosive and for non-nitrate-based explosives.
18 . The trace detection system of claim 17 , wherein said chamber comprises a first chamber within which said first ionization source operates, and a second volume, distinct from said first volume, within which said second ionization source operates.
19 . The trace detection system of claim 18 , wherein said spectrometer is further configured to screen ions from said first volume for the nitrate-based explosives, and to screen ions from said second volume for the non-nitrate-based explosives.
20 . The trace detection system of claim 16 , wherein said low-strength electric field is configured to:
liberate a free electron from a molecule of the gas; and accelerate the free electron to a first kinetic energy level, the first kinetic energy level insufficient to break chemical bonds of diatomic oxygen.
21 . (canceled)Join the waitlist — get patent alerts
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