Sensitivity traps for electronic trace detection having explosives or narcotics embedded in a plasticized polymer matrix

Patent metadata

Field	Value
Publication number	US-12411122-B2
Application number	US-202117318917-A
Country	US
Kind code	B2
Filing date	May 12, 2021
Priority date	May 12, 2020
Publication date	Sep 9, 2025
Grant date	Sep 9, 2025

Abstract

Embodiments of the present specification provide methods and systems for sensitivity traps that contain a polymer matrix made from an inert polymer material for encapsulation of trace amounts of explosives and narcotics and a suitable plasticizer material, the types and ratios of which may be selected based on type of analyte that is to be used with the sensitivity trap. The plasticizer material functions by breaking up intra and inter-molecular polymer chain interactions resulting in a larger diffusion coefficient of the analyte within the polymer matrix. Therefore, in embodiments, sufficient amounts of plasticizers are added to the sensitivity trap, which also reduces a glass transition temperature of the polymer matrix and the trap.

First claim

We claim:

1. A method of manufacturing a sensitivity trap, wherein the sensitivity trap comprises a polymer matrix made of a polymer material, and at least one analyte embedded within the polymer matrix, and wherein the sensitivity trap is defined by a target glass transition temperature, the method comprising:
selecting an amount and a type of plasticizer, wherein the amount and the type of the plasticizer is based upon a type of the at least one analyte and at least one of the target glass transition temperature or a diffusion coefficient of the at least one analyte and wherein said amount of plasticizer is sufficient to increase a diffusion coefficient of the at least one analyte such that, when the sensitivity trap is inserted into an ion mobility spectrometer (IMS) and exposed to a heating rate of approximately 33° C. per second, the at least one analyte is released from the mixture with sufficient desorption intensity to reach at least 2000 a.u. as measured by the IMS within 4 seconds of initiating heating;
dissolving a polymer and the selected amount and type of plasticizer in a solvent to form a mixture;
adding the at least one analyte to the mixture;
removing the solvent from the mixture; and
depositing the mixture onto a carrier to form the sensitivity trap.

2. The method of claim 1 , further comprising depositing a predefined amount of the mixture on a surface.

3. The method of claim 1 , wherein the at least one analyte comprises at least one of an explosive material, a narcotic material, or a combination of an explosive and a narcotic material.

4. The method of claim 1 , wherein an amount of the at least one analyte in the polymer matrix is less than 100 nanograms.

5. The method of claim 1 , wherein the at least one analyte comprises at least one of a nitroaromatic composition, a nitramine composition, a nitro-ester composition, a nitrate composition, or a peroxide composition.

6. The method of claim 1 , wherein the polymer is a polycarbonate composition.

7. The method of claim 6 , further comprising adjusting the target glass transition temperature.

8. The method of claim 7 , wherein the plasticizer is diisooctyl phthalate.

9. The method of claim 8 , wherein the target glass transition temperature is in a range of −30 to 140 degrees Celsius.

10. The method of claim 1 , further comprising determining a rate of release of the analyte from the sensitivity trap by adjusting the amount and type of the plasticizer.

11. The method of claim 1 , wherein the polymer material is a polycarbonate composition and wherein the plasticizer is diisooctyl phthalate.

12. The method of claim 11 , wherein the amount of the plasticizer is between 4 and 24 W t percent.

13. The method of claim 11 , wherein the amount of the plasticizer is approximately 14 W t percent.

14. The method of claim 1 , wherein the plasticizer is at least one of tributyl citrate, acetyl triethyl citrate, diisooctyl phthalate, or triisononyl trimellitate.

15. The method of claim 1 , wherein the polymer material is at least one of an inert organic polymer material, polystyrene, polycarbonate, or polylactic-co-glycolic acid.

16. The method of claim 1 , wherein the carrier comprises at least one of metal, glass and ceramic material.

17. A sensitivity trap defined by a target glass transition temperature, comprising:
a polymer matrix made of a polymer material;
at least one analyte embedded within the polymer matrix;
a plasticizer, wherein an amount and a type of the plasticizer is based upon the target glass transition temperature and a type of the at least one analyte and wherein said amount of plasticizer is sufficient to increase a diffusion coefficient of the at least one analyte such that, when the sensitivity trap is inserted into an ion mobility spectrometer (IMS) and exposed to a heating rate of approximately 33° C. per second, the at least one analyte is released from the mixture with sufficient desorption intensity to reach at least 2000 a.u. as measured by the IMS within 4 seconds of the onset of heating; and
a carrier material upon which the polymer matrix, at least one analyte, and plasticizer are deposited.

18. The sensitivity trap of claim 17 , wherein the at least one analyte comprises at least one of an explosive material, a narcotic material, or a combination of an explosive and a narcotic material.

19. The sensitivity trap of claim 18 , wherein the explosive material comprises at least one of a nitroaromatic composition, a nitramine composition, a nitro-ester composition, a nitrate composition, or a peroxide composition.

20. The sensitivity trap of claim 17 , wherein an amount of the at least one analyte in the polymer matrix is less than 100 nanogram in a solvent-cast membrane.

21. The sensitivity trap of claim 17 , wherein the polymer material is a polycarbonate composition and wherein the plasticizer is diisooctyl phthalate.

22. The sensitivity trap of claim 21 , wherein the amount of the plasticizer is between 4 and 24 W t percent.

23. The sensitivity trap of claim 21 , wherein the amount of the plasticizer is approximately 14 W t percent.

24. The sensitivity trap of claim 21 , wherein the glass transition temperature is in a range of −30 to 140 degrees Celsius.

25. The sensitivity trap of claim 17 , wherein the plasticizer is at least one of tributyl citrate, acetyl triethyl citrate, diisooctyl phthalate, or triisononyl trimellitate.

26. The sensitivity trap of claim 17 , wherein the polymer material is at least one of an inert organic polymer material, polystyrene, polycarbonate, or polylactic-co-glycolic acid.

27. The sensitivity trap of claim 17 , wherein the carrier material is at least one of metal, glass and ceramic.

Assignees

• Rapiscan Systems Inc

Inventors

• Verkerk Udo H
• Romanov Vladimir
• Schmidt Hartwig
• Lukow Stefan
• Macrae Robert
• Andersen Zachary

Classifications

• G01N33/15

  Medicinal preparations {; Physical properties thereof, e.g. dissolubility} · CPC title

• H01J49/0027

  Methods for using particle spectrometers · CPC title

• G01N27/622

  Ion mobility spectrometry · CPC title

• G01N27/62

  by investigating the ionisation of gases, e.g. aerosols; by investigating electric discharges, e.g. emission of cathode · CPC title

• G01N33/0011

  Sample conditioning (preparing specimens for investigation G01N1/28) · CPC title