A Modified Fast Analog Technique for Determining Luminescence Decay Times of Scintillators

1994 ◽  
Vol 348 ◽  
Author(s):  
L. Liu ◽  
W. Borst ◽  
C. Palsule ◽  
S. Gangopadhyay

ABSTRACTWe have modified our previous fast analog technique to determine the luminescence decay times of scintillators following an excitation with a Sr90β3-source. In the original technique [1], the sample was excited with a nitrogen-pumped dye laser, and the fluorescence pulses (consisting of typically 50 to 1000 photons) were detected by a multi-channel plate photomultiplier tube (MCP-PMT). The output from the MCP-PMT was directed to a fast waveform digitizer triggered externally by the exciting laser. In the modified technique, the digitizer acquires the fluorescence decay in the internal trigger mode, as no corresponding external trigger pulse is available from the Sr90source. For efficient light collection from scintillators, an ellipsoidal mirror assembly has been tested. The fluorescence decays are acquired as multi-photon pulses and are subsequently corrected for the temporal instrument response by using a deconvolution technique. The overall time resolution of the technique is about 100 ps. The fluorescence decay time obtained using this technique for a commercial scintillator (SCSN-81) agrees well with literature. We also discuss our results on new epoxy-polymer based scintillators prepared in our laboratory. The primary motivation for this work was development of new scintillators with shorter fluorescence decay times for high collision rate experiments.

1980 ◽  
Vol 12 (3) ◽  
pp. 263-266 ◽  
Author(s):  
E.J. Fairley ◽  
A.R. Spowart ◽  
B. Blanzat ◽  
J.P. Denis

1988 ◽  
Vol 43 (6) ◽  
pp. 583-590 ◽  
Author(s):  
Dieter Oelkrug ◽  
Klaus Rempfer ◽  
Ellen Prass ◽  
Herbert Meier

Abstract The absorption and fluorescence of three isomeric distyrylbenzenes are investigated as function of temperature. From the fluorescence decay times and fluorescence quantum yields two classes of oligostyrylarenes can be distinguished. A decisive criterion for this classification is, whether the first excited singlet state S1 belongs to an allowed or forbidden transition S0→S1.


1981 ◽  
Vol 36 (1) ◽  
pp. 30-33 ◽  
Author(s):  
J. Bendig ◽  
D. Kreysig ◽  
A. Kawski

The absorption spectra of the 3 isomeric aza- and the 4 isomeric azinium-anthracenes are discussed on the basis of the absorption anisotropy, the oscillator strenght and the fluorescence decay times. The influence of endocyclic substitution depends on the position of the aza- and aziniumgroup, respectively. In the case of acridine, acridinium, benzo[g]quinolinium and benzo[f]- isoquinolinium the S0 → S2-transition is observable. The spectra of benzo[g]quinoline, benzo[f]- isoquinoline and acridizinium are similar to those of anthracene


1954 ◽  
Vol 44 (3) ◽  
pp. 238 ◽  
Author(s):  
C. F. Ravilious ◽  
R. T. Farrar ◽  
S. H. Liebson

Science ◽  
1967 ◽  
Vol 156 (3777) ◽  
pp. 949-951 ◽  
Author(s):  
R. F. Chen ◽  
G. G. Vurek ◽  
N. Alexander

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