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Evaluation of wavelength shifters for spectral separation of barium fluoride emissions

dc.contributor.authorDeVol, T. A.en_US
dc.contributor.authorWehe, David K.en_US
dc.contributor.authorKnoll, Glenn F.en_US
dc.date.accessioned2006-04-10T17:57:13Z
dc.date.available2006-04-10T17:57:13Z
dc.date.issued1994-08-21en_US
dc.identifier.citationDeVol, T. A., Wehe, D. K., Knoll, G. F. (1994/08/21)."Evaluation of wavelength shifters for spectral separation of barium fluoride emissions." Nuclear Instruments and Methods in Physics Research Section A: Accelerators, Spectrometers, Detectors and Associated Equipment 348(1): 156-162. <http://hdl.handle.net/2027.42/31384>en_US
dc.identifier.urihttp://www.sciencedirect.com/science/article/B6TJM-473FVJB-C7/2/9e185124c33411fbe15a4028d2f92351en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/31384
dc.description.abstractApplication of the barium fluoride (BaF2) scintillator for characterization of intense radiation fields has been pursued since the fast component was discovered in the early 1980's. Unfortunately, ~ 80% of the scintillator emissions have a slow ~ 600 ns decay time constant. The long decay time hampers the use of BaF2 at high count rates because the slow emissions appear as an afterglow which has an intensity that varies with the interaction rate in the crystal. The temporal separation of BaF2 emissions by spectral separation using wavelength shifting techniques has been explored in this work. Of the wavelength shifting techniques that were examined, the solvent excitation technique showed the greatest potential, but was insufficient by itself to suppress the slow emissions to the desired degree. All the wavelength shifting techniques yield an enhanced ratio of fast to slow photons, but a decreased fast photoelectron yield.en_US
dc.format.extent576878 bytes
dc.format.extent3118 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypetext/plain
dc.language.isoen_US
dc.publisherElsevieren_US
dc.titleEvaluation of wavelength shifters for spectral separation of barium fluoride emissionsen_US
dc.typeArticleen_US
dc.rights.robotsIndexNoFollowen_US
dc.subject.hlbsecondlevelPhysicsen_US
dc.subject.hlbsecondlevelNuclear Engineering and Radiological Sciencesen_US
dc.subject.hlbtoplevelScienceen_US
dc.subject.hlbtoplevelEngineeringen_US
dc.description.peerreviewedPeer Revieweden_US
dc.contributor.affiliationumDepartment of Nuclear Engineering, The University of Michigan, Ann Arbor, MI 48109, USAen_US
dc.contributor.affiliationumDepartment of Nuclear Engineering, The University of Michigan, Ann Arbor, MI 48109, USAen_US
dc.contributor.affiliationumEnvironmental Systems Engineering Department, Clemson University, Anderson, SC 29625, USA; Department of Nuclear Engineering, The University of Michigan, Ann Arbor, MI 48109, USAen_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/31384/1/0000297.pdfen_US
dc.identifier.doihttp://dx.doi.org/10.1016/0168-9002(94)90854-0en_US
dc.identifier.sourceNuclear Instruments and Methods in Physics Research Section A: Accelerators, Spectrometers, Detectors and Associated Equipmenten_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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