Abstract

High-energy photon interrogation has established itself as a valuable tool for detecting special nuclear materials and characterizing nuclear waste. Previous research predominantly uses around 9-MV linear electron accelerators (LINACs) as photon sources and limited exploration has been conducted on the use of organic scintillators to determine the energy deposited in the detector and to separate photon and neutron radiation, crucial when the photon interrogation is based on the measurement of the neutron emission. The challenge arises from the intense photon flux typically produced by electron accelerators, resulting in issues such as pulse pile-up, detector saturation, and a suboptimal signal-to-background ratio. This study aims to extend the applicability of the conventional Active Photon Interrogation (API) techniques by introducing a novel method enabling the detection, in addition to nuclear materials, of light elements—specifically nitrogen, oxygen, and carbon—known to be present in conventional explosives, narcotics, and chemical weapons. The approach relies on active photon interrogation at high energies above 12 MeV, coupled with photoneutron spectrometry. Using a 22-MV electron LINAC, pulse shape discrimination with an organic liquid scintillator demonstrated promising performance. Our results highlight that the conventional pulse shape discrimination capabilities and rapid time-scale operation of organic scintillators enable the detection of fast neutrons from (γ,Xn) reactions, even in a mixed short-pulsed field of photon and neutron radiation with intense photon flashes. This exploration of the initial experimental aspects of photoneutron detection induced by high-energy photons establishes a foundation for a promising new method for the detection of illicit materials.

Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.