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Register a new userNeutron hardness of EJ-276 scintillation material
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This paper presents the results of the fast neutron irradiation (E$_n$ > 0.5MeV) of an EJ-276 scintillator performed in the MARIA research reactor with fluence up to 5.3$times$10$^{15}$ particles/cm$^2$. In our work, four samples with size $phi$25.4~mm$times$5~mm were tested. The changes in the light yield, emission and absorption spectrum and neutron/gamma discrimination using PuBe source before and after irradiation are presented. The figure of merit in neutron/gamma discrimination based on the charge integration method for different neutron fluences and different short gate integration times are determined.
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An organic glass scintillator developed by Sandia National Laboratories was characterized in terms of its light output and pulse shape discrimination (PSD) properties and compared to commercial liquid (EJ-309) and plastic (EJ-276) organic scintillators. The electron light output was determined through relative comparison of the $^{137}$Cs Compton edge location. The proton light yield was measured using a double time-of-flight technique at the 88-Inch Cyclotron at Lawrence Berkeley National Laboratory. Using a tunable broad-spectrum neutron source and an array of pulse-shape-discriminating observation scintillators, a continuous measurement of the proton light yield was performed for EJ-309 (200 keV$-$3.2 MeV), EJ-276 (170 keV$-$4.9 MeV), and the organic glass (50 keV$-$20 MeV). Finally, the PSD properties of the organic glass, EJ-309, and EJ-276 were evaluated using an AmBe source and compared via a figure-of-merit metric. The organic glass exhibited a higher electron light output than both EJ-309 and EJ-276. Its proton light yield and PSD performance were comparable to EJ-309 and superior to that of EJ-276. With these performance characteristics, the organic glass scintillator is well poised to replace current state-of-the-art PSD-capable scintillators in a range of fast neutron detection applications.
Ensuring the radiation hardness of PbWO4 crystals was one of the main priorities during the construction of the electromagnetic calorimeter of the CMS experiment at CERN. The production on an industrial scale of radiation hard crystals and their certification over a period of several years represented a difficult challenge both for CMS and for the crystal suppliers. The present article reviews the related scientific and technological problems encountered.
Ionization and scintillation produced by nuclear recoils in gaseous xenon at approximately 14 bar have been simultaneously observed in an electroluminescent time projection chamber. Neutrons from radioisotope $alpha$-Be neutron sources were used to induce xenon nuclear recoils, and the observed recoil spectra were compared to a detailed Monte Carlo employing estimated ionization and scintillation yields for nuclear recoils. The ability to discriminate between electronic and nuclear recoils using the ratio of ionization to primary scintillation is demonstrated. These results encourage further investigation on the use of xenon in the gas phase as a detector medium in dark matter direct detection experiments.
In this work we study the performance of silicon photomultiplier (SiPM) light sensors after exposure to the JULIC cyclotron proton beam, of energy $sim$ 39 MeV, relative to their performance before exposure. The SiPM devices used in this study show a significant change in their behavior and downward shift of their breakdown voltage by as much as $sim$ 0.4$pm$0.1 V. Single photon measurements appear to be no longer possible for the SiPMs under study after exposure to a dose of $sim$ 0.2 Gy (corresponding to an integrated proton flux of $sim$$phi_{p}$=1.06x10$^{8}$ p/cm$^{2}$). No visible damage to the surface of the devices was caused by the exposure.
Scintillation from noble gases is an important technique in particle physics including neutrino beam experiments, neutrino-less double beta-decay and dark matter searches. In liquid argon, the possibility of enhancing the light yield by the addition of a small quantity of xenon (doping at 10-1000 ppm) has been of particular interest. While the pathway for energy transfer between argon and xenon excimers is well known, the time-dependence of the process has not been fully studied in the context of a physics-based model. In this paper we present a model of the energy transfer process together with a fit to xenon-doped argon data. We have measured the diffusion limited rate constant as a function of xenon dopant. We find that the time dependence of the energy transfer is consistent with diffusion-limited reactions. Additionally, we find that commercially obtained argon can have a small xenon component (4 ppm). Our result will facilitate the use of xenon-doped liquid argon in future experiments.
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