We present the design, characterization, and testing of a laboratory prototype radiological search and localization system. The system, based on time-encoded imaging, uses the attenuation signature of neutrons in time, induced by the geometrical layout and motion of the system. We have demonstrated the ability to detect a ∼1mCi252Cf radiological source at 100m standoff with 90% detection efficiency and 10% false positives against background in 12min. This same detection efficiency is met at 15s for a 40m standoff, and 1.2s for a 20m standoff.
This is a high-risk effort to leverage knowledge gained from previous work, which focused on detector development leading to better energy resolution and reconstruction errors. This work seeks to enable applications that require precise elemental characterization of materials, such as chemical munitions remediation, offering the potential to close current detection gaps.
We present the design and performance of a proof-of-concept 32 channel material identification system. Our system is based on the energy-dependent attenuation of fast neutrons for four elements: hydrogen, carbon, nitrogen and oxygen. We describe a new approach to obtaining a broad range of neutron energies to probe a sample, as well as our technique for reconstructing the molar densities within a sample. The system's performance as a function of time-of-flight energy resolution is explored using a Geant4-based Monte Carlo. Our results indicate that, with the expected detector response of our system, we will be able to determine the molar density of all four elements to within a 20-30% accuracy in a two hour scan time. In many cases this error is systematically low, thus the ratio between elements is more accurate. This degree of accuracy is enough to distinguish, for example, a sample of water from a sample of pure hydrogen peroxide: the ratio of oxygen to hydrogen is reconstructed to within 8 0.5% of the true value. Finally, with future algorithm development that accounts for backgrounds caused by scattering within the sample itself, the accuracy of molar densities, not ratios, may improve to the 5-10% level for a two hour scan time. Experimental performance was evaluated with various thicknesses of polyethylene. The detector response in terms of energy, particle identification, and timing are presented as well.
We present the design and expected performance of a proof-of-concept 32 channel material identification system. Our system is based on the energy-dependent attenuation of fast neutrons for four elements: hydrogen, carbon, nitrogen and oxygen. We describe a new approach to obtaining a broad range of neutron energies to probe a sample, as well as our technique for reconstructing the molar densities within a sample. The system's performance as a function of time-of-flight energy resolution is explored using a Geant4-based Monte Carlo. Our results indicate that, with the expected detector response of our system, we will be able to determine the molar density of all four elements to within a 20–30% accuracy in a two hour scan time. In many cases this error is systematically low, thus the ratio between elements is more accurate. This degree of accuracy is enough to distinguish, for example, a sample of water from a sample of pure hydrogen peroxide: the ratio of oxygen to hydrogen is reconstructed to within 8±0.5% of the true value. Finally, with future algorithm development that accounts for backgrounds caused by scattering within the sample itself, the accuracy of molar densities, not ratios, may improve to the 5–10% level for a two hour scan time.
Dual plane neutron scatter cameras have shown promise for localizing fast neutron sources. The condition that a neutron must scatter in both planes of the camera produces low counting efficiencies. Counting efficiency can be improved using an alternative design that uses a single, optically segmented volume of scintillation material. Using Geant4, we simulated pulses from neutron elastic scatter events at different locations throughout an EJ-204 scintillator bar. We used nonlinear regression on low light pulses to determine the position along the bar where the scatter event occurred.
A transportable fast neutron detection system has been designed and constructed for measuring neutron energy spectra and flux ranging from tens to hundreds of MeV. The transportability of the spectrometer reduces the detector-related systematic bias between different neutron spectra and flux measurements, which allows for the comparison of measurements above or below ground. The spectrometer will measure neutron fluxes that are of prohibitively low intensity compared to the site-specific background rates targeted by other transportable fast neutron detection systems. To measure low intensity high-energy neutron fluxes, a conventional capture-gating technique is used for measuring neutron energies above 20 MeV and a novel multiplicity technique is used for measuring neutron energies above 100 MeV. The spectrometer is composed of two Gd containing plastic scintillator detectors arranged around a lead spallation target. To calibrate and characterize the position dependent response of the spectrometer, a Monte Carlo model was developed and used in conjunction with experimental data from gamma ray sources. Multiplicity event identification algorithms were developed and used with a Cf-252 neutron multiplicity source to validate the Monte Carlo model Gd concentration and secondary neutron capture efficiency. The validated Monte Carlo model was used to predict an effective area for the multiplicity and capture gating analyses. For incident neutron energies between 100 MeV and 1000 MeV with an isotropic angular distribution, the multiplicity analysis predicted an effective area of 500 cm2 rising to 5000 cm2. For neutron energies above 20 MeV, the capture-gating analysis predicted an effective area between 1800 cm2 and 2500 cm2. The multiplicity mode was found to be sensitive to the incident neutron angular distribution.
Nuclear Instruments and Methods in Physics Research, Section A: Accelerators, Spectrometers, Detectors and Associated Equipment
Sweany, Melinda D.; Dazeley, S.; Askins, M.; Bergevin, M.; Bernstein, A.; Bowden, N.S.; Jaffke, P.; Rountree, S.D.; Shokair, T.M.
Here we present the first results of WATCHBOY, a water Cherenkov detector designed to measure the yield of β-neutron emitting radionuclides produced by cosmic ray muons in water. In addition to the β-neutron measurement, we also provide a first look at isolating single-β producing radionuclides following muon-induced hadronic showers as a check of the detection capabilities of WATCHBOY. The data taken over 207 live days indicates a 9Li production yield upper limit of 1.9× 10-7μ-1g-1 cm2 at ∼400 m water equivalent (m.w.e.) overburden at the 90% confidence level. In this work the 9Li signal in WATCHBOY was used as a proxy for the combined search for 9Li and 8He production. This result will provide a constraint on estimates of antineutrino-like backgrounds in future water-based antineutrino detectors.
We present a neutron detector system based on time-encoded imaging, and demonstrate its applicability toward the spatial mapping of special nuclear material. We demonstrate that two-dimensional fast-neutron imaging with 2° resolution at 2 m stand-off is feasible with only two instrumented detectors.
Material Identification by Resonant Attenuation is a technique that measures the energy-dependent attenuation of 1-10 MeV neutrons as they pass through a sample. Elemental information is determined from the neutron absorption resonances unique to each element. With sufficient energy resolution, these resonances can be used to categorize a wide range of materials, serving as a powerful discrimination technique between explosives, contraband, and other materials. Our proposed system is unique in that it simultaneously down-scatters and time tags neutrons in scintillator detectors oriented between a d-T generator and sample. This allows not only for energy measurements without pulsed neutron beams, but for sample interrogation over a large range of relevant energies, vastly improving scan times. Our system’s core advantage is a potential breakthrough ability to provide detection discrimination of threat materials by their elemental composition (e.g. water vs. hydrogen peroxide) without opening the container. However, several technical and computational challenges associated with this technique have yet to be addressed. There are several open questions: what is the sensitivity to different materials, what scan times are necessary, what are the sources of background, how do each of these scale as the detector system is made larger, and how can the system be integrated into existing scanning technology to close current detection gaps? In order to prove the applicability of this technology, we will develop a validated model to optimize the design and characterize the uncertainties in the measurement, and then test the system in a real-world scenario. This project seeks to perform R&D and laboratory tests that demonstrate proof of concept (TRL 3) to establishing an integrated system and evaluating its performance (TRL 4) through both laboratory tests and a validated detector model. The validated model will allow us to explore our technology’s benefits to explosive detection in various applications.
This note summarizes an effort to characterize the effects of adding water-based liquid scintillator to the WATCHMAN detector. A detector model was built in the Geant4 Monte Carlo toolkit, and the position reconstruction of positrons within the detector was compared with and without scintillator. This study highlights the need for further modeling studies and small-scale experimental studies before inclusion into a large-scale detector, as the benefits compared to the associated costs are unclear.
A spallation based multiplicity detector has been constructed and deployed to the Kimballton Underground Research Facility to measure the cosmogenic fast neutron flux anti-coincident from the initiating muon. Two of the three planned measurements have been completed (~380 and ~600 m.w.e) with sufficient statistics. The third measurement at level 14 (~4450 m.w.e.) is currently being performed. Current results at ~600 m.w.e. compare favourably to the one previous measurement at 550 m.w.e. For neutron energies between 100 and 200 MeV measurements at ~380 m.w.e. produce fluxes between 1e-8 and 7e-9 n/cm2/s/MeV and at ~600 m.w.e. measurements produce fluxes between 7e-9 and 1e-11 n/cm2/s/MeV.
Antineutrino monitoring of nuclear reactors has been demonstrated many times, however the technique has not as of yet been developed into a useful capability for treaty verification purposes. The most notable drawback is the current requirement that detectors be deployed underground, with at least several meters-water-equivalent of shielding from cosmic radiation. In addition, the deployment of liquid-based detector media presents a challenge in reactor facilities. We are currently developing a detector system that has the potential to operate above ground and circumvent deployment problems associated with a liquid detection media: the system is composed of segments of plastic scintillator surrounded by 6LiF/ZnS:Ag. ZnS:Ag is a radio-luminescent phosphor used to detect the neutron capture products of lithium-6. Because of its long decay time compared to standard plastic scintillators, pulse-shape discrimination can be used to distinguish positron and neutron interactions resulting from the inverse beta decay (IBD) of antineutrinos within the detector volume, reducing both accidental and correlated backgrounds. Segmentation further reduces backgrounds by identifying the positron’s annihilation gammas, which are absent for most correlated and uncorrelated backgrounds. This work explores different configurations in order to maximize the size of the detector segments without reducing the intrinsic neutron detection efficiency. We believe this technology will ultimately be applicable to potential safeguards scenarios such as those recently described.
