Bismuth-charged structured solid organic scintillator

Abstract

A scintillator for imaging using X-rays or gamma rays or charged particles, includes a network of glass capillaries with an inner diameter no greater than 500 micrometers. The capillaries are filled with a polymer material made up of at least (i) a monomer selected from the group comprising vinyltoluene, styrene and vinylxylene and the isomers thereof, (ii) a cross-linking agent made up of a divinylbenzene or a dimethacrylate having a central chain which includes 1 to 12 carbon atoms, and (iii) triphenylbismuth. The cross-linking agent is provided to make up 10 wt % to 60% wt of the mixture thereof with the monomer, and the triphenylbismuth makes up at least 5 wt %. The cross-linking agent is provided in a ratio of 0.75 to 2.25 times the weight content of the triphenylbismuth.

Claims

1. A scintillator for imaging using X-rays or gamma-rays or charged particles, comprising: a network of glass capillaries having an inner diameter at most equal to 500 micrometers, the capillaries filled with a polymer material comprising at least, (i) a monomer selected from the group constituted by vinyltoluene, styrene and vinylxylene and their isomers, (ii) a cross-linking agent constituted by a dimethacrylate having a central chain comprising from 1 to 12 carbon atoms or by divinylbenzene, and (iii) triphenylbismuth, wherein the polymer material includes 10 wt. % to 60 wt. % cross-linking agent in combination with the monomer, and at least 5 wt. % triphenylbismuth, and a proportion of the cross-linking agent is 0.75 to 1.25 times the weight of triphenylbismuth.

2. The scintillator according to claim 1, wherein the cross-linking agent is divinylbenzene.

3. The scintillator according to claim 1, wherein the cross-linking agent is 1,4 butanediyl dimethacrylate.

4. The scintillator according to claim 1, wherein the polymer material comprises the monomer and the cross-linking agent in a weight ratio of between 2 and 4.

5. The scintillator according to claim 4, wherein the monomer and the cross-linking agent are in a weight ratio of between 2.9 and 3.1.

6. The scintillator according to claim 1, wherein the cross-linking agent and the triphenylbismuth are in a weight ratio of between 0.9 and 1.1.

7. The scintillator according to claim 1, wherein the polymer material further comprises at least 8 wt. % Bi.

8. The scintillator according to claim 1, wherein the polymer material further comprises at least one fluorophore capable of generating light in the visible spectrum.

9. The scintillator according to claim 1, wherein a face of the scintillator opposite an X-ray or gamma-ray or charged-particle ray includes a reflective coating suitable for reflecting light towards the other face.

10. The scintillator according to claim 9, wherein the capillaries include an internal coating of a reflective material.

11. The scintillator according to claim 1, wherein a face of the scintillator opposite an X-ray or gamma-ray or charged-particle ray includes a scattering coating suitable for sending light towards the other face.

12. The scintillator according to claim 11, wherein the capillaries include an internal coating of a reflective material.

13. The scintillator according to claim 1, wherein the capillaries have an inner diameter no more than 20 micrometers.

Description

BRIEF DESCRIPTION OF THE DRAWING

(1) Objects of the invention will become apparent from the following description, given by way of non-limitative illustrative example, in the light of the attached drawing in which:

(2) FIG. 1 is a graph representing the decay (in arbitrary units) of the signal emitted against time for a scintillator in accordance with the invention,

(3) FIG. 2a is a diagram of a bare capillary

(4) FIG. 2b is a diagram of a capillary provided with a reflective coating on the rear face

(5) FIG. 2c is a diagram of a capillary the inner surface of which comprises a reflective coating

(6) FIG. 2d is a diagram of a capillary combining a reflective coating on the inner wall and a reflective or light-scattering coating on the rear face,

(7) FIGS. 3a to 3c are figures showing illuminance corresponding to the capillaries of FIGS. 2a to 2c,

(8) FIG. 3d is a figure showing illuminance corresponding to the case of a capillary according to FIG. 2d with a reflective coating,

(9) FIG. 3e is a figure showing illuminance corresponding to the case of a capillary according to FIG. 2d with a light-scattering coating.

DETAILED DESCRIPTION

(10) In general, the invention consists of producing structured organic scintillators from a mixture comprising at least one monomer selected from the following monomers (including their isomers): Vinyltoluene Styrene Vinylxylene
to which is added at least one cross-linking agent chosen from the group constituted by divinylbenzene and dimethacrylates having a central chain comprising 1 to 12 carbon atoms (such as 1,4 butanediyl dimethacrylate), while respecting the condition that the proportions of cross-linking agent and of monomer are comprised between 10%-60% and 90%-40%, with respect to the mixture of monomers and of constituents. This means that there may be from 10% to 60% of cross-linking agent, with respect to the mixture of monomers and of cross-linking agent.

(11) After adding an appropriate proportion of triphenylbismuth (in practice at least equal to 5% by weight of the mixture of monomer and cross-linking agent and triphenylbismuth), an organic scintillator is obtained that combines the advantages of a capillary scintillator and a high-Z scintillator: in fact, this scintillator combines a good spatial resolution and a good sensitivity, without involving a significant thickness, and without the risk of deterioration of the transparency over time.

(12) The content of cross-linking agent is advantageously selected as a function of the triphenylbismuth content, in practice between 0.75 and 2.25 times this content, preferably between 0.9 and 1.1 times this content, which amounts to saying that, preferably, the content of cross-linking agent is at least approximately equal to the triphenylbismuth content.

(13) A scintillator of the aforementioned type has an intrinsic light emission in the UV when it is subjected to an ionizing radiation. This is why one option of the invention consists of incorporating fluorophores into the organic material of the scintillator in order to convert the preferential emission in the UV thereof to the red region. This makes it possible to adapt the scintillator to the image sensors such as CCD sensors for example.

(14) The fluorophores used in the invention are preferably derivatives of 1,8-naphthalimide.

(15) Without wishing to be limited thereto, it is noteworthy that particularly useful results have been obtained by using two primary fluorophores, 2,5-diphenyloxazole or biphenyl.

(16) Very particularly advantageously, the invention utilizes another fluorophore which is either a compound with a structure close to the naphthalimides (bis-N-(2,5-di-t-butylphenyl)-3,4,9,10-perylenetetracarbodiimide), or Nile Red.

(17) Other fluorophores can be envisioned provided that the energy transfers are carried out from the near UV to the red region with a good quantum efficiency, determined by the overlapping of the successive emission/absorption spectra.

(18) It is noteworthy that the set of fluorophores provided above make it possible to retain a decay time of the order of approximately ten nanoseconds.

(19) Thus, the invention makes it possible to develop plastic scintillators the wavelength of which is easily adjustable. In other words, it is possible according to the invention to add up to three or even four different fluorophores, which convert the incident radiant energy from the UV to the red region.

(20) To this end it is possible to select: A first fluorophore (primary fluorophore) that is soluble in the apolar solvents at concentrations comprised between 0.5 and 15% by weight, preferably between 3% and 15% by weight, having a maximum absorption wavelength close to 300 nm and emitting light at around 360 nm, having a quantum efficiency of fluorescence greater than 20% and a luminescence decay constant less than 20 ns; A second fluorophore (secondary fluorophore) that is soluble in the apolar solvents at concentrations comprised between 0.01 and 4% by weight, having a maximum absorption wavelength close to 360 nm and emitting light at around 420 nm, having a quantum efficiency of fluorescence greater than 40% and a luminescence decay constant less than 20 ns; A third fluorophore (tertiary fluorophore) that is soluble in the apolar solvents at concentrations comprised between 0.01 and 1% by weight, having a maximum absorption wavelength close to 420 nm and emitting light at around 510 nm, having a quantum efficiency of fluorescence greater than 40% and a luminescence decay constant less than 20 ns; A fourth fluorophore (quaternary fluorophore) that is soluble in the apolar solvents at concentrations comprised between 0.01 and 1% by weight, having a maximum absorption wavelength close to 510 nm and emitting light at around 590 nm, having a quantum efficiency of fluorescence greater than 40% and a luminescence decay constant less than 20 ns.

(21) FIG. 1 represents a time-resolved measurement of the spectrum for an excitation of the scintillator at 330 nm, expressing a measurement of the decay time of the scintillator. The decay profile over time at the wavelength of interest is measured then approximated by a single or double decreasing exponential function. The decay time is then defined as the time constant of the first exponential function.

(22) The capillary matrix utilized in the invention is made from glass, in practice according to a staggered arrangement, with optional spacers between the capillaries. The utilization of capillaries made from plastic material cannot be envisioned because in the vast majority of cases the glass transition temperature is below 100° C. or very slightly above (with the notable exception of the family of polycarbonates). As the polymerization of the heavy-metal loaded scintillators passes through thermal cycles exceeding 100° C., the integrity of the assembly cannot then be ensured.

(23) The optical index of the heavy-metal loaded organic scintillator is close to 1.57. The index of the glass constituting the cladding must therefore be less than this value in order to ensure guiding according to Snell-Descartes law. As scintillation is intrinsically isotropic, the waveguide thus constituted must have a numerical aperture (the formula of which is provided below) that is as high as possible in order to reduce unguided light losses. To this end, the index of the glass constituting the cladding must be well below that of the index of the scintillating plastic.

(24) $\mathrm{NA}=\sqrt{n_c^2-n_{\mathrm{cl}}^2}\mathrm{with}\{\begin{array}{c}{n}_c\mathrm{core}\mathrm{index}\\ n_{\mathrm{cl}}\mathrm{cladding}\mathrm{index}\end{array}$

(25) FIG. 2a shows a capillary comprising a glass tube 1 (the index n is substantially equal to 1.47) and a polymerized material 2 (in the case in question, its index n was 1.57); an X-ray coming from the right is intercepted there within the material, at a site denoted by the arrow P, so as to generate a photon flowing towards the left, while being reflected off the inner surface of the capillary.

(26) According to an advantageous feature of the invention, a reflective layer 3 is added on the face of the scintillator which, being perpendicular to the capillary matrix, is in direct view of the ionizing radiation; this makes it possible to recover the light propagating in the opposite direction to the X-ray (see FIG. 2b, in comparison with the basic configuration in FIG. 2a).

(27) According to another advantageous feature of the invention, between the capillaries or along their inner surface a material (not shown) is added, absorbing the visible light in order to reduce the cross-talk between waveguides. As the scintillation is isotropic, while the waveguide constituted by the scintillating core and the glass cladding has a limited acceptance angle, the addition of the absorbent also reduces unguided stray light, thereby improving the spatial resolution.

(28) According to yet another variant, a reflective metallic deposit 4 is formed on the inner walls of the glass capillaries (see FIG. 2c). In fact, while the previous versions lose over 50% of the light signal due to the limited acceptance angle of the step-index waveguide, the addition of the reflective deposit allows the light generated by the scintillator to be guided with a minimum of loss. Nevertheless, due to the scintillator/air interface, a portion of the guided light remains trapped inside the waveguide. In order to recover this light, the inventors provide, moreover, to add a mirror 3 or a light-scattering coating 5 on the rear face of the capillary matrix (see FIG. 2d).

(29) The benefit of the aforementioned additions is apparent from comparison of FIGS. 3a to 3e: FIG. 3a shows the illumination map obtained for a waveguide formed from a bare capillary, for a 1 W isotropic point source in the middle of the guide, with a linear color scale from 0 to 7.7 10.sup.6 W/m.sup.2 (the measured loss was 89%), FIG. 3b shows the illumination map obtained under the same conditions, in the case of a capillary equipped with a mirror on the rear face (FIG. 2b); the measured loss was 76%, FIG. 3c shows the illumination map obtained under the same conditions, in the case of a capillary the inner surface of which is made reflective (FIG. 2c); the measured loss was 88%, FIG. 3d shows the illumination map obtained under the same conditions, in the case of a capillary combining an inner reflective surface and a mirror on the rear face (FIG. 2d); the measured loss was 76%, and FIG. 3e shows the illumination map obtained under the same conditions, in the case of a capillary combining an inner reflective surface and a light-scattering coating on the rear face (FIG. 2d); the measured loss was 14%.

(30) It is noteworthy that, in comparison with the case of a bare capillary, the presence of a reflective coating on the inside of the capillary has practically no effect (it seems that, in the case in question, the inner surface of the capillary already had a significant reflective effect). The presence of a mirror on the rear face has a positive effect; on the other hand, surprisingly, the losses are significantly reduced by placing a scatter material on the rear face.

(31) By way of example, an organic scintillator is produced from a poly(styrene)-poly(1,4-butanediyle dimethacrylate) mixture placed in the presence of a determined proportion of triphenylbismuth; the glass used for the glass capillaries (reference 8250 from the manufacturer Schott) has an optical index of 1.57. The numerical aperture of the bundle of scintillating fibers then creates a numerical aperture of 0.52 corresponding to an angle of 31.6°. The glass capillaries have an inner diameter of at most 100 μm, or even less than 50 μm, or even at most equal to 20 or even 10 μm In order to avoid too large an inhomogeneity of illumination of the scintillator, a strict control of the thickness of the glass (difference between outer/inner diameter) and of the glass index was carried out. In fact, a wide divergence of this thickness leads to significant fluctuations in density and index between capillaries.

(32) Fluorophores are incorporated in order to maximize the fluorescence intensity under X-rays. The best scintillation yields were obtained for weight percentages of bismuth close to 10%.

(33) A particular example of composition is given below, in a ratio of 8% Pb:

(34) TABLE-US-00001 % by weight of styrene 60 % by weight of 1,4 butanediyl dimethacrylate 20 % by weight of triphenylbismuth 20 % by weight of bismuth 8.18 % by weight of PPO 15 % by weight of N-(2′,5′-di-t-butylphenyl)-4- 0.3 butylamino-1,8-naphthalimide % by weight of bis-N-(2′,5′-di-t-butylphenyl)- 0.02 3,4,9,10-perylenetetracarbodiimide λ absorption (nm) <500 λ max fluorescence (nm) 580 Decay time (ns) 6

(35) The contents are given with reference to the mixture of the first three constituents; the monomer and the cross-linking agent are present here in a weight ratio of 2/1, while the cross-linking agent has a content by weight equal to that of the triphenylbismuth.

(36) Similar proportions can be utilized for a mixture of vinyltoluene (or of vinylxylene) with 1,4 butanediyl dimethacrylate (or another dimethacrylate having a central chain comprising from 1 to 12 carbon atoms), or with divinylbenzene as cross-linking agent, while achieving satisfactory results.

(37) Preferably, the scintillator of the invention has a maximum emission towards wavelengths above 570 nm. By way of example, the fluorescent compounds incorporated into the scintillators studied are derivatives of 1,8-naphthalimides, perylene carbodiimides and Nile Red.

(38) In a simplified version of the invention, it is possible to prepare scintillators fluorescing in any visible wavelength range whatsoever.

(39) By way of example, in order to produce a bismuth scintillator defined above, pure 1,4 butanediyl dimethacrylate, pure styrene, triphenylbismuth, N-(2′,5′-di-t-butylphenyl)-4-butylamino-1,8-naphthalimide, bis-N-(2′,5′-di-t-butylphenyl)-3,4,9,10-perylenetetracarbodiimide and 2,5-diphenyloxazole are mixed under inert atmosphere in a dry flask. The mixture is fully degassed using the method known as “freeze-pump-thaw”, then it is poured carefully into a mold having the dimensions of the capillary matrix, which will give the final form of the scintillator.

(40) The capillary matrix, the inner diameter of which is a few tens of micrometers (at most 20, or even 10 micrometers), is then introduced into the mold so that the liquid forcibly enters the spaces left free in the glass matrix over a length of several centimeters.

(41) The preparation of the mixture, its introduction into the mold, then the introduction of the capillary matrix are carried out at ambient temperature, a temperature at which good solubilization of the various constituents of the mixture is ensured.

(42) After a heat cycle adapted to putting the scintillator into form and allowing all the monomers to polymerize, the product is removed from the mold, then polished until a surface condition is obtained that is compatible with imaging applications. The dimensions of the scintillator are, for example, 40 mm in length and width (perpendicularly to the length of the capillaries) and 5 mm thick (parallel to these capillaries). The main emission wavelength is 580 nm.