Plastic scintillator materials, plastic scintillators comprising such materials and method for distinguishing neutrons from gamma rays using said scintillators

Patent metadata

Field	Value
Publication number	US-9453160-B2
Application number	US-201414773176-A
Country	US
Kind code	B2
Filing date	Mar 6, 2014
Priority date	Mar 7, 2013
Publication date	Sep 27, 2016
Grant date	Sep 27, 2016

Abstract

A plastic scintillator material, a plastic scintillator prepared by shaping the material, a detection portal, and a method for discrimination a signal due to fast neutrons. The plastic scintillator material including a polymeric matrix into which is incorporated at least one fluorescent compound at a mass concentration greater than or equal to 10% by mass of the total mass of the material. The polymeric matrix comprises a crosslinked polymer obtainable by polymerization of a mixture comprising at least one aromatic monomer and at least one monomer which is a crosslinking agent selected from the group consisting of an alkyl diacrylate, an alkyl dimethacrylate, and a mixture thereof, and molar proportions of the crosslinking monomer and of the aromatic monomer in the mixture are from 10% to 50% and from 90% to 50%, respectively.

First claim

The invention claimed is:

1. A plastic scintillator material, comprising a polymeric matrix into which is incorporated at least one fluorescent compound at a mass concentration greater than or equal to 10% by mass of the total mass of the material,
wherein:
the polymeric matrix comprises a crosslinked polymer obtainable by polymerization of a mixture comprising at least one aromatic monomer and at least one monomer which is a crosslinking agent selected from the group consisting of an alkyl diacrylate, an alkyl dimethacrylate, and a mixture thereof; and
molar proportions of the crosslinking monomer and of the aromatic monomer in the mixture are from 10% to 50% and from 90% to 50%, respectively.

2. The material according to claim 1 , wherein the molar proportions of the crosslinking monomer and of the aromatic monomer in the mixture are from 15% to 20% and from 85% to 80%, respectively.

3. The material according to claim 1 , wherein the aromatic monomer is selected from the group consisting of styrene, a styrene substituted with one or several alkyl group(s), vinylnaphtalene, vinylnaphtalene substituted with one or several alkyl group(s), N-vinylcarbazole, and a mixture thereof.

4. The material according to claim 3 , wherein the styrene substituted with one or several alkyl group(s) is selected from the group consisting of t-butylstyrene and its isomers, vinyltoluene and its isomers, and vinylxylene and its isomers.

5. The material according to claim 1 , wherein the crosslinking monomer is 1,4-butanediyl dimethacrylate.

6. The material according to claim 1 , wherein the polymeric matrix comprises, as a fluorescent compound, a first fluorescent compound which is a compound having an absorption spectrum for which the maximum absorption intensity is located between 250 nm and 350 nm, and an emission spectrum which is located between 340 nm and 400 nm.

7. The material according to claim 6 , wherein the first fluorescent compound is biphenyl.

8. The material according to claim 6 , wherein the first fluorescent compound is present in an amount from 10% to 30% by mass, relative to a total mass of the material.

9. The material according to claim 6 , wherein the polymeric matrix further comprises a second fluorescent compound having an absorption spectrum covering the emission spectrum of the first fluorescent compound, and an emission spectrum which is located between 350 nm and 650 nm, and having a maximum emission intensity between 400 and 600 nm.

10. The material according to claim 9 , wherein the second fluorescent compound is selected from the group consisting of bis-methylstyryl benzene (bis-MSB), 1,4-di-[2-(5-phenyloxazolyl)]benzene (POPOP), 9,10-diphenyl anthracene, 4-ethoxy-N-(2′,5′-di-t-butylphenyl)-1,8-naphthalimide and 3-hydroxyflavone.

11. The material according to claim 9 , wherein the second fluorescent compound is present in an amount from 0.01% to 1% by mass, relative to a total mass of the material.

12. The material according to claim 9 , wherein the polymeric matrix further comprises a third fluorescent compound having an absorption spectrum covering the emission spectrum of the second fluorescent compound, and having an emission spectrum for which the maximum emission intensity is located between 500 nm and 650 nm.

13. The material according to claim 12 , wherein the third fluorescent compound is selected from the group consisting of perylene, 4-butylamino-N-(2′,5′-di-t-butylphenyl)-1,8-naphthalimide, a cumarin compound, and acridine yellow.

14. The material according to claim 13 , wherein the cumarin compound is selected from the group consisting of cumarins 1, 6, 30, 102, 151, 314, and 343.

15. The material according to claim 12 , wherein the third fluorescent compound is present in an amount from 0.001% to 0.1% by mass, relative to a total mass of the material.

16. The material according to claim 1 , comprising:
a first fluorescent compound at a concentration of 16.65% by mass of the total mass of the material;
a second fluorescent compound at a concentration from 0.01% to 0.3% by mass; and
in a polymeric matrix comprising a polymer of styrene in an amount of 66.62% by mass of the total mass of the material and of 1,4-butanediyl dimethacrylate, in an amount of 16.65% by mass of the total mass of the material.

17. The material according to claim 16 , wherein
the first fluorescent compound is biphenyl,
the second fluorescent compound is bis-methylstyrylbenzene or 1,4-di[2(5-phenyloxazolyl)]benzene (POPOP), and
the third fluorescent compound is perylene or 4-butylamino-N-(2′,5′-di-t-butylphenyl)-1,8-naphthalimide.

18. The material according to claim 16 , further comprising: a third fluorescent compound at a concentration from 0.002% to 0.05% by mass of the total mass of the material.

19. The material according to claim 1 , wherein the polymeric matrix further comprises at least o boron-containing compound.

20. The material according to claim 19 , wherein the mass concentration of the boron-containing compound is from 1% to 10%.

21. A plastic scintillator prepared by shaping the material according to claim 1 .

22. A plastic scintillator prepared by shaping the material according to claim 19 .

23. A method for discriminating from each other, a signal due to fast neutrons, a signal due to thermal neutrons, and a signal due to gamma rays in a radiation comprising fast neutrons, thermal neutrons and gamma rays emitted by a mixed source, the method comprising:
exposing the plastic scintillator of claim 22 to said radiation emitted by the mixed source; and
separating the signal due to fast neutrons from the signal due to thermal neutrons, and from the signal due to gamma rays, by pulse shape discrimination (PSD).

24. The plastic scintillator according to claim 22 , wherein the scintillator has a volume greater than or equal to 1 L.

25. The plastic scintillator according to claim 21 , wherein the scintillator has a volume greater than or equal to 1 L.

26. A detection portal, comprising the plastic scintillator according to claim 21 .

27. A method for discriminating a signal due to fast neutrons from a signal due to gamma rays in a radiation comp sing fast neutrons and gamma rays emitted by a mixed source, the method comprising:
exposing the plastic scintillator of claim 21 to said radiation emitted by the mixed source; and
separating the signal due to fast neutrons from the signal due to gamma rays by pulse charge discrimination (PSD).

Assignees

• Commissariat Energie Atomique
• Commissariat L Energie Atomique Et Aux Energies Alternatives

Inventors

• Hamel Matthieu
• Blanc Pauline
• Normand Stephane
• Dehe-Pittance Chrystele

Classifications

• C08K5/1545

  Six-membered rings · CPC title

• C09K2211/1096

  containing other heteroatoms · CPC title

• C09K11/06 Primary

  containing organic luminescent materials · CPC title

• C09K11/025

  non-luminescent particle coatings or suspension media · CPC title

• C08K5/3437

  condensed with carbocyclic rings · CPC title