Deuterated-xylene (xylene-d10; EJ301D): A new, improved deuterated liquid scintillator for neutron energy measurements without time-of-flight

التفاصيل البيبلوغرافية
العنوان: Deuterated-xylene (xylene-d10; EJ301D): A new, improved deuterated liquid scintillator for neutron energy measurements without time-of-flight
المؤلفون: R.S. Raymond, Siobhán Clarke, Michael Febbraro, R. O. Torres-Isea, A. Di Fulvio, Fredrick D. Becchetti, Sara A. Pozzi
المصدر: Nuclear Instruments and Methods in Physics Research Section A: Accelerators, Spectrometers, Detectors and Associated Equipment. 820:112-120
بيانات النشر: Elsevier BV, 2016.
سنة النشر: 2016
مصطلحات موضوعية: Physics, Nuclear and High Energy Physics, Deuterated benzene, Physics::Instrumentation and Detectors, 010308 nuclear & particles physics, Analytical chemistry, Scintillator, 01 natural sciences, Neutron temperature, Neutron spectroscopy, law.invention, Nuclear physics, Time of flight, chemistry.chemical_compound, chemistry, law, 0103 physical sciences, Van de Graaff generator, Neutron detection, Neutron, 010306 general physics, Instrumentation
الوصف: In conjunction with Eljen Technology, Inc. (Sweetwater,TX) we have designed, constructed, and evaluated a 3 in. ×3 in. deuterated-xylene organic liquid scintillator (C8D10; EJ301D) as a fast neutron detector. Similar to deuterated benzene (C6D6; NE230, BC537, and EJ315) this scintillator can provide good pulse-shape discrimination between neutrons and gamma rays, has good timing characteristics, and can provide a light spectrum with peaks corresponding to discrete neutron energy groups up to ca. 20 MeV. Unlike benzene-based detectors, deuterated xylene is less volatile, less toxic, is not known to be carcinogenic, has a higher flashpoint, and hence is much safer for many applications. In addition EJ301D can provide slightly more light output and better PSD than deuterated-benzene scintillators. We show that, as with deuterated-benzene scintillators, the light-response spectra can be unfolded to provide useable neutron energy spectra without need for time-of-flight (ToF). An array of these detectors arranged at many angles close to a reaction target can be much more effective (×10 to ×100 or more) than an array of long-path ToF detectors which must utilize a narrowly-bunched and pulse-selected beam. As we demonstrate using a small Van de Graaff accelerator, measurements can thus be performed when a bunched and pulse-selected beam (as needed for time-of-flight) is not available.
تدمد: 0168-9002
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::e96616c196228694db046e852a32adfb
https://doi.org/10.1016/j.nima.2016.02.058
حقوق: OPEN
رقم الأكسشن: edsair.doi...........e96616c196228694db046e852a32adfb
قاعدة البيانات: OpenAIRE