Accession Number:

AD1083460

Title:

Enabling Mobile Neutron Detection Systems with CLYC

Descriptive Note:

Technical Report,01 Oct 2016,12 Sep 2019

Corporate Author:

AIR FORCE INSTITUTE OF TECHNOLOGY WRIGHT-PATTERSON AFB OH WRIGHT-PATTERSON AFB United States

Personal Author(s):

Report Date:

2019-09-12

Pagination or Media Count:

138.0

Abstract:

Cs2LiYCl6Ce3 CLYC has the desirable property of being sensitive to both gamma rays and neutrons while producing waveforms suitable for pulse shape discrimination PSD to determine which radiation was detected. This dissertation examines the behavior of CLYC to support its further development for mobile and portable applications. First, the feasibility of performing PSD with CLYC and an inexpensive data acquisition system was examined. This system was able to clearly distinguish both events with a figure of merit of 1.42. Next, the performance of a SiPM was compared to a traditional PMT. Analysis showed that the SiPM degraded the energy resolution by an average of 34.00.7 at 662 keV. Measurements were also taken using a CLYC crystal with two optical windows which was rotated to determine the direction of a neutron source with an accuracy of 10. An analysis of the ability of clustering algorithms to discriminate between gamma ray and neutron interactions was also performed. A methodology was developed and applied to separate these two interactions and provide the ability to isolate the 35Cln,p35S interaction with thermal neutrons, which occurs close to the gamma ray region and is difficult to separate visually. Finally, the effect of temperature on a 7Li 99 enriched CLYC crystal important when the 35Cl n,p35S interaction is more desirable than 6Lin,t interaction was examined. Measurements agreed with previous results from 6Li 95 enriched CLYC, but also indicated that identifying the cluster corresponding to thermal neutrons interacting with 35Cl was temperature dependent.

Subject Categories:

  • Nuclear Physics and Elementary Particle Physics

Distribution Statement:

APPROVED FOR PUBLIC RELEASE