Device and method for analysis of material by neutron interrogation
10527561 ยท 2020-01-07
Assignee
Inventors
Cpc classification
G01V5/234
PHYSICS
G01V5/22
PHYSICS
G01N23/20066
PHYSICS
G01N23/2208
PHYSICS
G01N23/20
PHYSICS
International classification
G01V5/00
PHYSICS
G01N23/20066
PHYSICS
G01N23/20
PHYSICS
Abstract
Material analysis device (100) comprising a neutron generator (10) for emitting neutrons towards a material to be analysed in pulsed mode; an alpha particle detector (13) for locating the neutrons emitted in a given solid angle by detecting alpha particles associated with these neutrons; at least one gamma ray detector (14) for measuring energy of gamma photons generated by interaction of the neutrons emitted in the given solid angle with the material to be analysed; at least two Compton cameras (15), each for measuring energy of the gamma photons generated by interaction of the neutrons with the material to be analysed and for calculating an incidence cone of these gamma photos; and an electronic circuit adapted for three-dimensionally mapping the presence of at least one chemical element of interest in the material to be analysed based on data provided by the alpha particle detector (13), the gamma ray detector (14) and the Compton cameras (15).
Claims
1. Material analysis device comprising: a neutron generator for emitting neutrons towards a material to be analysed, wherein the neutron generator comprises a neutron tube equipped with an electrical supply enabling the neutron generator to operate in pulsed mode; an alpha particle detector allowing location of neutrons emitted at a given solid angle by detecting alpha particles associated with these neutrons; at least one gamma ray detector for measuring energy of gamma photons generated by interaction of the neutrons emitted in the given solid angle with the material to be analysed; at least two Compton cameras each for measuring energy of gamma photons generated by neutron interaction with the material to be analysed and for calculating an incidence cone of these gamma photons; an electronic circuit adapted for three-dimensionally mapping the presence of at least one chemical element of interest in the material to be analysed based on data provided by the alpha particle detector, the gamma ray detector and the Compton cameras.
2. Material analysis device according to claim 1, wherein the electronic circuit is configured to implement a method of analysis by associated particle imaging, or API method, and a method of thermal neutron analysis, or TNA method, in order to three-dimensionally map the presence of the chemical element(s) of interest.
3. Material analysis device according to claim 1, wherein the electronic circuit processes energy measurements provided by the gamma ray detector and/or at least one of the Compton cameras for selecting the chemical element of interest among elements constituting the material to be analysed.
4. Material analysis device according to claim 1, wherein the electronic circuit executes a three-dimensional localisation algorithm in which only data relating to the chemical element of interest, among data provided by the Compton cameras, are used as algorithm input data.
5. Material analysis device according to claim 1, wherein the electronic circuit executes a three-dimensional localisation algorithm in which only data associated with the chemical element of interest, among data provided by the alpha particle detector, are used as algorithm input data.
6. Material analysis device according to claim 1, combined with a displacement system adapted to create a relative movement between the device and the material to be analysed.
7. Vehicle equipped with a material analysis device according to claim 1.
8. Material analysis method employing a material analysis device according to claim 1.
9. Material analysis method according to claim 8, comprising the following stages: emission at a moment t of neutrons towards the material to be analysed, by means of the neutron generator operating in pulsed mode; data acquisition by the alpha particle detector and the gamma ray detector (14) within a time window t that follows moment t; data acquisition by the Compton cameras, within a time window t that follows moment t+t; and processing of the acquired data to produce three-dimensional mapping of the presence of the chemical element of interest in the material to be analysed.
10. Material analysis method according to claim 9, wherein the data processing implements a method of analysis by associated particle imaging, or API method, and a method of thermal neutron analysis, or TNA method, in order to produce said three-dimensional mapping.
11. Material analysis method according to claim 9, wherein, before the three-dimensional mapping is performed, the chemical element of interest is selected from among elements constituting the material to be analysed by analysing the energy measurements provided by the gamma ray detector and/or at least one of the Compton cameras.
12. Material analysis method according to claim 9, wherein only data relating to the chemical element of interest, among data provided by the Compton cameras, are used as input data of a three-dimensional localisation algorithm.
13. Material analysis method according to claim 9, wherein only data associated with the chemical element of interest, among data provided by the alpha particle detector, are used as input data of a three-dimensional localisation algorithm.
14. Material analysis method according to claim 9, used to detect explosive substances, wherein the chemical element of interest is characteristic of an explosive substance.
Description
BRIEF DESCRIPTION OF THE DRAWINGS
(1) The appended drawings are schematic and are not to scale; their purpose is above all to illustrate the principles of the invention.
(2) In these drawings, from one figure (FIG) to another, identical elements (or parts of elements) are identified by the same reference signs.
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DETAILED DESCRIPTION OF EXAMPLES
(9) Exemplary embodiments are described in detail below, with reference to the appended drawings. These examples illustrate the characteristics and advantages of the invention. It should be remembered however that the invention is not limited to these examples.
(10) An example of a material analysis device is illustrated schematically in
(11) The two Compton cameras 15 and the gamma ray detectors 14 can be arranged radially around the neutron source of the neutron generator 10, as shown in
(12) The device 100 may be arranged over the surface 101A of the material 101 to be analysed, as illustrated in
(13) The neutron generator 10 emits neutrons towards the material 101 to be analysed. It comprises a neutron tube 11 equipped with an electrical supply 12. The electrical supply 12 enables the neutron generator 10 to operate in pulsed mode.
(14) The neutron tube 11 exploits, for example, the fusion reaction between a deuterium nucleus (D or deuton) and a tritium nucleus (T or triton) to generate neutrons, as shown by the following equation: D+T.fwdarw.n+.
(15) Collision between a deuterium nucleus and a tritium nucleus provides a neutron n with an energy of approximately 14 MeV and simultaneously, an alpha particle with an energy of approximately 3.5 MeV. Consequently and according to the laws of conservation of energy and quantity of motion, a neutron emitted along a path 201 is associated with an alpha particle along a path 202 at 180 to the path 201, as shown in
(16) A neutron tube 11 may comprise a target 23, a deuterium and/or tritium reservoir 20, an ion source 21 and an accelerating electrode 22. The target 23 is the site of the nuclear reaction between the deuterium and/or tritium nuclei of which it is composed and a beam of incident deuterons and/or tritons (or their molecular form). In order to cause the beam of deutons and/or tritons to collide with the target 23, the beam of deutons and/or tritons is accelerated by an intense electrical field resulting from application of a major voltage difference between the target (cathode) 23 and the accelerating electrode (anode) 22. The beam of deutons and/or tritons is preferably obtained by means of an ion source 22 in which a gaseous mixture of deuterium and tritium originating from the reservoir 20 is ionised. The ions thus generated are subsequently extracted in the acceleration space, forming the beam of deutons and/or tritons.
(17) The neutron tube 11 is equipped with a high voltage electrical supply 12 to generate an intense electrical field resulting from application of a major voltage difference between the target (cathode) 23 and the accelerating electrode (anode) 21. The electrical supply 12 operates in pulsed mode. Pulsed mode means that the electrical supply emits a THT voltage for a pulse duration t.sub.0 and subsequently the electrical supply no longer emits any voltage for a duration t.sub.1. In pulsed mode, this voltage change from 0 to a non-zero THT value is repeated periodically. The THT emitted by the electrical supply causes acceleration of the beam of deutons and/or tritons on the cable and thus emission of neutrons for the pulse duration t.sub.0. Then, no neutrons are emitted for the duration t.sub.1. This is known as operation of the neutron generator in pulsed mode. Neutron emission pulsation can also be obtained by maintaining a direct THT voltage between the target 23 and the accelerating electrode 21. In the latter case, it is the electrical supply of the ion source 21 that operates in pulsed mode, being increased periodically to a HT voltage for a pulse duration t.sub.0 and subsequently zeroed for a duration t.sub.1.
(18) As mentioned above and with reference to
(19) The alpha particle detector 13 may for example be an Yttrium Aluminium Perovskite (YAP) scintillator, equipped with a set of photomultiplier tubes or a multianode photomultiplier tube. The analysis device 100 could comprise several alpha particle detectors 13.
(20) The neutron emitted by the neutron generator 10 will interact with the material to be analysed 101 by multiple interactions. The first interaction of the neutron with the material 101 will almost instantaneously generate emission of a gamma photon (). The energy of this gamma photon will depend on the atom of the material that has interacted with the neutron. Thus, measuring the energy of the gamma photon will allow identification of the nature of the atom. Furthermore, the temporal coincidences between the alpha particles detected at a moment t.sub. and the gamma rays resulting from the first interaction detected at a moment t.sub. are analysed. Knowing the solid angle of emission of the neutron and the speeds of the particles involved (for example 1 cm/ns for particles of 3.5 MeV, 5 cm/ns for neutrons of 14 MeV and 30 cm/ns for photons ), the geometric configuration of the system (relative positions of the alpha particle detector and the gamma ray detector with respect to the target 23 emitting neutrons), it is possible to identify a three-dimensional pixel, or voxel, containing the atom that interacted with the neutron in question. This method corresponds to the method of analysis by detection of associated alpha particles, or API method, mentioned above.
(21) The gamma ray detectors 14 allow detection and measurement of the energy of the gamma photons emitted by interaction between the neutrons and the material and thus establishment of the energetic spectrum of these gamma rays. A gamma ray detector may comprise, for example, a scintillating crystal, a photomultiplier and an electronic circuit. The scintillating crystal, or scintillator, may be of the LaBr.sub.3, BGO or NaI type, etc. and of sufficient volume to completely arrest incident gamma rays of up to some ten MeV of energy for example. The photomultiplier may be a silicon-based digital component consisting of a matrix in which each pixel is an independent photomultiplier. The electronic circuit can perform a first level of processing of the signal, allowing construction of an energy spectrum.
(22) The resolution of the API method will depend on the resolution in (x, y) of the alpha ray detection matrix and the time bins considered during the test for coincidence (time of flight of the neutron). Thus, each useful coincidence identified is associated with a voxel of the medium. By measuring each time the energy E.sub. of the gamma photon which is the source of this coincidence, the system determines an energy spectrum that can be used mathematically (deconvolution, spectral decomposition or search for specific lines) to estimate the elemental chemical composition of this voxel and thereby determine the nature of the material analysed.
(23) The data obtained by the API method, which utilises the initial interaction between the neutrons and the material to be analysed, will be supplemented by the data obtained using the so-called TNA (Thermal Neutron Analysis) method presented below, which utilises the last interaction between the neutrons and the material.
(24) When a neutron passes through the material to be analysed, it gives up much of its energy as multiple diffusion reactions (elastic or inelastic) occur. This deceleration by a succession of collisions with the nuclei of the material is known as thermalisation. After a certain period of time, typically ranging from a few microseconds to a few hundred microseconds (which is considerable compared to the period of a few nanoseconds elapsing between emission and the first interaction), the neutron has an increasing probability of being absorbed by a nucleus of the medium. When this absorption is accompanied by the prompt emission of a gamma photon, this is called radiative capture.
(25) The gamma photons obtained from the radiative captures are detected by the two Compton cameras 15 in order to obtain information on three-dimensional localisation of the nucleus which is the source of the radiative capture.
(26) Generally speaking, a Compton camera comprises a first part known as the diffuser and a second part known as the absorber. An incident photon of a certain energy undergoes initial Compton scattering in the diffuser. Following other interactions, the scattered photon is finally absorbed in the absorber. The operating principle of the Compton cameras 15 is illustrated in the diagram in
(27) When a gamma photon of incident energy E.sub.0 enters the scintillator 31, it has a non-zero probability of undergoing Compton scattering. During this scattering, an energy E.sub.1 is transferred to the medium. This energy E.sub.1 and the position of interaction are measured by the first scintillator 31. If, following the initial Compton scattering, the photon continues its travel to the second scintillator 32, it can then undergo a second Compton scattering during which it gives up an energy E.sub.2 and subsequently further Compton scatterings or other mechanisms of interaction such as the photoelectric effect or the creation of pairs until its entire remaining energy has been given up, e.g. it gives up the energies E.sub.3, . . . , E.sub.N, where N is a whole number greater than or equal to four in this example. With the position of the second Compton interaction and the total energy deposited by the second photomultiplier 34, it is possible to know the angle between the line traversed by the initial incident gamma photon and the direction defined by the two Compton interaction points by means of the following relationship:
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Where M.sub.e is the mass of the electron at rest, c is the speed of light in free space and E.sub.0=E.sub.1+E.sub.2+E.sub.3+ . . . +E.sub.N.
(29) Thus, for a photon of energy E.sub.0, the Compton camera calculates the half angle of the cone defining all possible directions of incidence of this photon. By analysing a sufficient quantity of events corresponding to the same initial energy E.sub.0 and if the original source of these photons is relatively ad hoc, the most probable direction of incidence of these photons of energy E.sub.0 can be calculated by integrating all the cones calculated at each event.
(30) Total deposition in the second scintillator 32 of the energy remaining after interaction in the first scintillator 31 is a particularity of the Compton cameras 15, compared with the gamma ray detectors 14 in which the entire initial energy E.sub.0 of the gamma photons can be deposited in the single scintillator of the detector 14. In order to ensure that the total energy is deposited in the second scintillator 32, the latter must be of sufficient size (typically on the order of 1 L) to ensure that the entire energy of the gamma photon is deposited, even for very high energies (up to 11 MeV).
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(32) Advantageously, only the data relating to gamma photons of a highly specific energy, corresponding to radiative capture by one or more chemical elements of interest among all the constituent elements of the material to be analysed, undergo treatment, so that only these elements of interest are located in the material. By way of an example, nitrogen and/or chlorine isotopes, which are found in the chemical composition of many explosives, may be involved.
(33) Indeed, the localisation algorithms of the API method and above all of the TNA method may be complex and the associated processing times may be longue. Therefore, it is advantageous to restrict the input data of these algorithms to the data relating to the chemical element of interest. For this purpose, a broad energy spectrum representative of the composition of the material 101 can be rapidly produced by the gamma ray detectors 14 and/or the Compton cameras 15. This may be an energy spectrum obtained from the initial interaction between the neutrons and the material, or the radiative capture of the neutrons. In particular, the gamma ray detectors 14 are used to produce an energy spectrum, for example for energies corresponding to radiative capture of the neutrons.
(34) The aforementioned localisation algorithms are applied by one or more circuits associated with the detectors 13, 14 and with the cameras 15. These circuits can be completely or partly integrated in the detectors and cameras, or be completely or partly external circuits. These electronic circuits include, for example, microprocessors, computer memories and a set of connections to link the electronic components of the circuits, the detectors 13, 14 and the cameras 15. All these circuits form an electronic circuit within the meaning of the present disclosure.
(35) The angle of orientation of the Compton cameras 15 in relation to the surface of the material to be analysed determines the analysis depth for which the capture gamma ray detection efficiency is optimal. Hence, orientation mechanisms are provided to vary the angle of orientation of the Compton cameras 15 with respect to the surface of the material to be analysed. Such mechanisms allow exploration of the material at different depths.
(36) Owing to their design and in particular, the fact that they include a scintillator and a photomultiplier, Compton cameras 15 can also help to determine the energy spectrum of the gamma photons in the API method. On other words, Compton cameras 15 can not only be used for the TNA method, but also to replace or supplement gamma ray detectors 14 in implementing the API method. In such a case, Compton cameras 15 play a dual role. This makes it possible to reduce the number of gamma ray detectors 14 used. It should be noted however that it is not economically viable to replace all the gamma ray detectors 14 with Compton cameras 15, since the latter are more costly than the gamma ray detectors 14 in this type of device.
(37) An exemplary method for analysis of material by neutron interrogation is illustrated in
(38) It should be noted that the neutron generator operates in pulsed mode so as not to confuse the gamma rays obtained from the initial interactions (inelastic diffusions) of the neutrons with the material to be analysed with those obtained from the last interactions (radiative captures) of the neutrons with the material to be analysed. Both these types of interaction are characterised by different times: the first occurs a few nanoseconds after emission of the neutrons and the last occurs a few microseconds to a few hundreds of microseconds after emission of the neutrons. Thus, a first time window t is defined when emission of the neutrons is in progress in order to identify the gamma rays generated by the first interaction and of which the origin can be traced by the associated alpha particle and a second time window t is defined in the absence of neutron emission in order to measure the energy of the gamma rays generated by the last interaction.
(39) The embodiments or examples described in the present disclosure are provided by way of illustration and are non-restrictive; a person skilled in the art can easily, in the light of this disclosure, modify these embodiments or examples, or contemplate others, while remaining within the scope of the invention.
(40) Furthermore, the different characteristics of the embodiments or examples described in the present disclosure may be considered separately or combined with each other. When combined, these characteristics may be combined as described above or differently, the invention not being limited to the specific combinations described above. In particular, unless otherwise specified or technically incompatible, a characteristic described in relation to one embodiment or example may be applied in a manner similar to another embodiment or example.