79 research outputs found

    Mathematical Removal of Positron Range Blurring in High Resolution Tomography

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    Monte Carlo Calculations of the Optical Coupling between Bismuth Germanate Crystals and Photomultiplier Tubes

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    Scintillation of tantalate compounds

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    A screening of 63 metal-tantalate-oxides was conducted in search of heavy scintillator materials operating at ambient temperature. While tantalates are known to have slow scintillation decay times, the high atomic number of tantalum (73) provides good stopping power for gamma rays. Screened samples were synthesized by solid state reactions. Scintillation properties of these materials were evaluated by X-ray diffraction, X-ray excited luminescence and pulsed X-ray luminescence. Of the 63 synthesized tantalates examined only 12 had luminosity values greater than 1000 ph/MeV at room temperature. From these, ScTaO4, YTa3O9, and Zn3Ta2O8 have greater than 40% of their emission in the first μs. The brightest and fastest compound of those tested was Zn3Ta2O8 with an estimated luminosity of 26,000 ph/MeV and a main decay time of 600 ns from its crystalline powder. Further attention is given to Zn3Ta2O8 and Mg4Ta2O9 scintillation properties, demonstrating their potential for scintillation applications

    Temperature dependence of CsI(Tl) gamma-ray excited scintillation characteristics

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    The gamma-ray excited, temperature dependent scintillation characteristics of CsI(Tl) are reported over the temperature range of -100 to + 50[deg]C. The modified Bollinger-Thomas and shaped square wave methods were used to measure the rise and decay times. Emission spectra were measured using a monochromator and corrected for monochromator and photocathode spectral efficiencies. The shaped square wave method was also used to determine the scintillation yield as was a current mode method. The thermoluminescence emissions of CsI(Tl) were measured using the same current mode method. At room temperature, CsI(Tl) was found to have two primary decay components with decay time constants of [tau]1 = 679+/-10 ns (63.7%) and [tau]2 = 3.34+/-0.14 [mu]s (36.1%), and to have emission bands at about 400 and 560 nm. The [tau]1 luminescent state was observed to be populated by an exponential process with a resulting rise time constant of 19.6+/-1.9 ns at room temperature. An ultra-fast decay component with a 1 and [tau]2 were determined to be 2.22+/-0.33 [mu]s and 18.0+/-2.59 [mu]s, respectively, while the 400 nm emission band was not observed below -50[deg]C. At +50[deg]C the decay constants were found to be 628 ns (70.5%) and 2.63 [mu]s (29.3%) and both emission bands were present. The scintillation yield of CsI(Tl) was observed to be only slightly temperature dependent between -30 and +50[deg]C, peaking at about -30[deg]C (about 6% above the room temperature yield) and monotonically decreasing above and below this temperature. Four different commercially available CsI(Tl) crystals were used. Minimal variations in the measured scintillation characteristics were observed among these four crystals. Thermoluminescence emissions were observed to have peak yields at -90, -65, -40, +20, and possibly -55[deg]C. The relative magnitudes and number of thermoluminescence peaks were found to vary from crystal to crystal.Peer Reviewedhttp://deepblue.lib.umich.edu/bitstream/2027.42/30984/1/0000659.pd
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