Lanthanide doped barium phosphorous oxide scintillators
The present invention provides for a composition comprising an inorganic scintillator comprising a lanthanide-doped barium phosphorous oxide useful for detecting nuclear material.
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The present invention provides for a composition comprising an inorganic scintillator comprising a lanthanide-doped barium phosphorous oxide useful for detecting nuclear material.
Nuclear facilities sometimes use hand-held plastic scintillator detectors to detect attempts to divert special nuclear material in situations where portal monitors are impractical. MCNP calculations have been performed to determine the neutron and gamma radiation field arising from a Category I quantity of weapons-grade plutonium in various shielding configurations. The shields considered were composed of combinations of lead and high-density polyethylene such that the mass of the plutonium plus shield was 22.7 kilograms. Monte-Carlo techniques were also used to determine the detector response to each of the shielding configurations. The detector response calculations were verified using field measurements of high-, medium-, and low- energy gamma-ray sources as well as a Cf-252 neutron source.
The present invention provides for a composition comprising an inorganic scintillator comprising a lanthanide-doped strontium barium mixed halide useful for detecting nuclear material.
The present invention provides for a composition comprising an inorganic scintillator comprising an optionally lanthanide-doped strontium-barium, optionally cesium, halide, useful for detecting nuclear material.
In one embodiment, a transparent ceramic of sintered nanoparticles includes gadolinium lutetium oxide doped with europium having a chemical composition (Lu.sub.1-xGd.sub.x).sub.2-YEu.sub.YO.sub.3, where X is any value within a range from about 0.05 to about 0.45 and Y is any value within a range from about 0.01 to about 0.2, and where the transparent ceramic exhibits a transparency characterized by a scatter coefficient of less than about 10%/cm. In another embodiment, a transparent ceramic scintillator of sintered nanoparticles, includes a body of sintered nanoparticles including gadolinium lutetium oxide doped with a rare earth activator (RE) having a chemical composition (Lu.sub.1-xGd.sub.x).sub.2-YRE.sub.YO.sub.3, where RE is selected from the group consisting of: Sm, Eu, Tb, and Dy, where the transparent ceramic exhibits a transparency characterized by a scatter coefficient of less than about 10%/cm.
The present invention provides for a composition comprising an inorganic scintillator comprising a lanthanide-doped strontium barium mixed halide useful for detecting nuclear material.
The present invention relates to sorohalide compounds having formula A.sub.3B.sub.2X.sub.9, where A is an alkali metal, B is a rare earth metal, and X is a halogen. Optionally, the sorohalide includes a dopant D. Such undoped and doped sorohalides are useful as scintillation materials or phosphors for any number of uses, including for radiation detectors, solid-state light sources, gamma-ray spectroscopy, medical imaging, and drilling applications.
A bulk semiconducting scintillator device, including: a Li-containing semiconductor compound of general composition Li-III-VI.sub.2, wherein III is a Group III element and VI is a Group VI element; wherein the Li-containing semiconductor compound is used in one or more of a first mode and a second mode, wherein: in the first mode, the Li-containing semiconductor compound is coupled to an electrical circuit under bias operable for measuring electron-hole pairs in the Li-containing semiconductor compound in the presence of neutrons and the Li-containing semiconductor compound is also coupled to current detection electronics operable for detecting a corresponding current in the Li-containing semiconductor compound; and, in the second mode, the Li-containing semiconductor compound is coupled to a photodetector operable for detecting photons generated in the Li-containing semiconductor compound in the presence of the neutrons.
The Deep Underground Neutrino experiment will conduct a broad program of physics research by studying a beam of neutrinos from Fermilab, atmospheric neutrinos, neutrinos from potential supernovae, and potential nucleon decay events. In pursuit of these studies, the experiment will deploy four 10kt fiducial mass liquid argon time projection chambers underground in Lead, South Dakota. Liquid argon time projection chambers allow high-resolution tracking and energy measurements. A precise timing signal is needed to provide the necessary time stamp to localize events in the drift direction. As liquid argon is a natural scintillator, a photon detection system will be deployed to provide such a signal, especially for non-beam events. In the baseline design for the single-phase time projection chamber, the detectors are contained within the anode plane assemblies. The design of two prototypes utilizing wavelength shifters and light guides are presented, and aspects of the research and development program are discussed.
We present a multi-channel, fast neutron/gamma ray detector array system that utilizes ZnS(Ag) scintillator detectors. The system employs field programmable gate arrays (FPGAs) to do real-time all digital neutron/gamma ray discrimination with pulse height and time histograms to allow count rates in excess of 1,000,000 pulses per second per channel. The system detector number is scalable in blocks of 16 channels.
According to one embodiment, a scintillator includes a host material having the chemical formula: A 2 BX 6 , where A includes a monovalent ion, B includes a tetravalent ion, and X includes a halide ion.
One of the primary goals of scintillator-based gamma-ray detector development is to obtain spatial resolutions in bulk crystals at the millimeter level in all three spatial dimensions. An even more challenging goal is to disentangle multiple simultaneous energy depositions with comparable spatial resolutions. We are exploring a new technique to achieve this level of performance through the use of close-coupled, coded-aperture shadow masks placed between the crystal and a position-sensitive phototransducer. We report on simulations of such a device using Monte Carlo light transport simulations performed with GEANT4. Initial indications are promising; however, the technique will require a very high level of performance from the phototransducer.
A chalcopyrite, colquiriite, neutron absorber loaded glass, or plastic scintillator based fiber optic plate for use in a neutron imaging system, including: a plurality of optical fiber segments disposed side-by-side adjacent to one another in a parallel array; and a binder material disposed between and coupling the plurality of optical fiber segments together. A diffuse reflective material is optically coupled to the plurality of first ends of the plurality of optical fiber segments. An optical detector device is optically coupled to the plurality of second ends of the plurality of optical fiber segments opposite the diffuse reflective material. Optionally, the fiber optic plate further includes a diffuse reflective material disposed one or more of on an exterior surface of each of the plurality of optical fiber segments and between the plurality of optical fiber segments.
A single crystal composition includes an alkali halide crystal doped with a divalent element in the amount of 0.5 to 5 weight percent, the doped crystal having an optical transmission of at least 45% at at least one wavelength. An alkali halide doped with at least one of europium and ytterbium is particularly useful as a scintillator.
The present invention provides for a composition comprising an inorganic scintillator comprising a doped halide, useful for detecting nuclear material.
We have developed radionuclide identification algorithms for radiation portal monitor applications. One algorithm uses a spectral angle mapper to match the power spectral density of modified cumulative distribution functions of measured pulse height distributions to reference spectra, while the others rely on the decomposition of the observed spectrum as a linear mixture of known radionuclide spectra. Three algorithms were then tested for their ability to perform on-the-fly radionuclide identification on datasets acquired with a liquid organic scintillator-based pedestrian radiation portal monitor on moving special nuclear material and industrial radiological sources, as well as common medical isotopes. We quantified and compared the relative efficacies of the algorithms considered using F-score analysis. Measured radiation sources included 51 g of highly enriched uranium, 6.6 g of weapons grade plutonium, 241 Am, 133 Ba, 57 Co and 137 Cs sources with activities of several hundred kBq, as well as 260 kBq liquid solution samples of the medical isotopes 99m Tc, 111 In, 67 Ga, 123 I, 131 I, and 201 Tl. We achieved 100% positive identification, for three-second measurements of single sources moving at a source-transit speed of 1.2 m/s. For mixed sources with strongest and weakest sources having no more than a 5:1 ratio of detected counts, encouraging positive identification results were achieved with the un-mixing algorithms. Current radiation portal monitor designs suffer from a high incidence rate of nuisance radiation alarms caused in radiation portal monitor primary screenings by recent nuclear medicine patients and cargo containing large amounts of naturally occurring radioactive materials. Integrating reliable on-the-fly radionuclide identification into the radiation portal monitors could lower the number of nuisance alarms requiring time-consuming secondary inspections.
A mixed compound glass scintillator includes a first compound and a second compound. The first compound has a Tg greater than 25° C., is organic, is capable of generating luminescence in the presence of ionizing radiation. The first compound includes a central species and a luminescent organic group bonded to the central species or to an optional organic linker group. The central species is selected from the group consisting of: carbon, silicon, and tin. The optional organic linker group, if present, is bonded to the central species and the luminescent organic group. The second compound also has a Tg greater than 25° C. The first and second compound are mixed and melted to form a glass material.
The present invention provides for a composition comprising an inorganic scintillator comprising an optionally lanthanide-doped barium mixed halide, useful for detecting nuclear material.