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Thermoluminescence of natural quartz
Get PDFThe kinetic and dosimetric features of the main thermoluminescence peak of quartz have been investigated in unannealed as well in quartz annealed at 500˚C for 10 minutes. The main peak is found at 92 and 86˚C respectively for aliquots of unannealed and annealed samples irradiated to 10 Gy and heated at 5.0˚C/s. For each sample, the intensity of the main peak is enhanced with repetitive measurement whereas its maximum temperature is unaffected. The peak position of the main peak in each sample is independent of the irradiation dose and this, together with its fading characteristics are consistent with first-order kinetics. For low doses, typically between 2 and 10 Gy, the dose response of the main peak in each sample is linear. In the intermediate dose range from 10 to 60 Gy, the growth of the main peak in each sample is sub-linear and for greater doses, in the range from 60 Gy to 151 Gy, it is linear again. The half-life of the main peak of the unannealed sample is about 1.3 h whereas that of the annealed sample is about 1.2 h. The main peak in each sample can be approximated to a first-order glow peak. As the heating rate increases, the intensity of the main peak in each sample decreases. This is evidence of thermal quenching. The main peak in each sample is the only peak regenerated by phototransfer. The resulting phototransferred peak occurs at the same temperature as the original peak and has similar kinetic and dosimetric features. For a preheat temperature of 120˚C, the intensity of the phototransferred peak in each sample increases with illumination time up to a maximum and decreases afterwards. At longer illumination times (such as 30 min up to 1 h), no further decrease in the intensity of the phototransferred peak is observed. The traps associated with the 325˚C peak are the main source of the electrons responsible for the regenerated peak. Radioluminescence emission spectra were also measured for quartz annealed at various temperatures. Emission bands in quartz are affected by annealing and irradiation. A strong enhancement of the 3.4 eV (~366 nm) emission band is observed in quartz annealed at 500˚C. A new emission band which grows with annealing up to 1000˚C is observed at 3.7 eV (~330 nm) for quartz annealed at 600˚C. An attempt has been made to correlate the changes in radioluminescence emission spectra due to annealing with the influence of annealing on luminescence lifetimes in quartz
Thermoluminescence of the main peak in SrAl2O4: Eu2+, Dy3+: spectral and kinetics features of secondary emission detected in the ultra-violet region
No full textWe report the thermoluminescence of SrAl2O4:Eu2+,Dy3+ measured in the ultra-violet region of the spectrum between 300 and 400 nm. Complementary measurements of X-ray excited optical luminescence confirm emission bands of stimulated luminescence in this region. As a further test, optically stimulated luminescence was also measured in this region. The glow curve measured at 1 °C s−1 following irradiation to various doses appears simple and single but is in reality a collection of several components. This was shown by results from the Tm-Tstop method on both ends of the peak, application of thermal cleaning beyond the peak maximum as well as the dependence of the peak on fading. The latter shows that new peaks appear as preceding ones fade. Kinetic analysis of some of the main peaks was carried out giving an activation energy of 0.6 eV. The implication of the results on measurement of phosphorescence, interpretation of dose response and fading is discussed
Phosphorescence of orthopaedic–grade ultra high molecular weight polyethylene
Get PDFIsothermal luminescence decay curves have been measured from orthopaedic–standard ultra high molecular weight polyethylene between 35 and 70 ˚C on the rising edge of the main glow peak at 70 ˚C. Preparatory peak-shape analysis of the temperature-resolved glow peak at 70 ˚C measured at 1 ˚C s–1 gave a geometrical factor close to 0.5 suggestive of second order kinetics for both the isothermal and thermally stimulated luminescence. The results of analysis of the phosphorescence of transformed monotonic-to-peak isothermal decay curves are also second order, as is the conclusion from thermoluminescence glow-curve de-convolution. All methods of analysis give an activation energy of about 0.7 eV
On the correlation between annealing and variabilities in pulsed-luminescence from quartz
Get PDFProperties of luminescence lifetimes in quartz related to annealing between 500 and 900ºC have been investigated. The luminescence was pulse-stimulated at 470 nm from sets of granular quartz annealed at 500, 600, 700, 800, and 900ºC. The lifetimes decrease with annealing temperature from about 42 to 33 µѕ when the annealing temperature is increased from 500 to 900ºC. Luminescence lifetimes are most sensitive to duration of annealing at 600ºC, decreasing from 40.2 ± 0.7 µѕ by as much as 7 µѕ when the duration of annealing is changed from 10 to 60 min. However, at 800–900ºC lifetimes are essentially independent of annealing temperature at about 33 µѕ. Increasing the exciting beta dose causes an increase in the lifetimes of the stimulated luminescence in the sample annealed at 800ºC but not in those annealed at either 500 or 600ºC. The temperature-resolved distribution of luminescence lifetimes is affected by thermal quenching of luminescence. These features may be accounted for with reference to two principal luminescence centres involved in the luminescence emission process
Concerning secondary thermoluminescence peaks in α-Al_2_O_3_:C
Get PDFThermoluminescence characteristics of two subsidiary glow peaks, one below 100°C and the other above 300°C, have been studied for measurements between 30°C and 500°C in α-Al_2_O_3_:C. The thermoluminescence intensity of the lower temperature peak decreased with storage with a half-life of about 150 s. In contrast, the intensity of the higher temperature peak increased with storage towards some maximum. The peak-temperature of each of the secondary glow peaks was essentially constant with dose, whereas that of the main peak decreased with irradiation. The dose response for the three peaks was similar except for sublinear growth in the higher temperature peak at low dose values. These effects are discussed in terms of changes in the concentration of F+ luminescence precursors brought about by competitive electron retrapping at deep electron-traps or hole-traps. This work refines the physics and application of α-Al_2_O_3_:C luminescence in radiation dosimetry
Orthopaedic grade ultra–high molecular weight polyethylene: some features of the main thermoluminescence glow curve
Get PDFThermoluminescence (TL) characteristics of orthopaedic–grade ultra–high molecular weight polyethylene have been investigated between 20 and 200_C. The TL at 1_C s_1 consists of two glow curves, a weaker intensity peak at 115_C and the main peak at 70_C, studied in this work. TL intensity increases with beta irradiation but with a dose–response influenced by heating rate. On the other hand, the peak maximum is affected by both irradiation and repeated use of a sample. The glow curve shifts to higher temperatures with increase in heating rate but only slightly so with change in beta irradiation dose, properties suggestive of first-order kinetics. Kinetic analysis for activation energy and order of kinetics, based on the discrete trap model, produce somewhat conflicting results. Whereas qualitative analysis of peak symmetry show that first-order kinetics apply, geometrical analysis of the peak shape suggests that the order of kinetics might be other than first-order. Values of activation energy evaluated using the initial rise method were found to be dose dependent and for a given beta dose are in agreement with calculations from peak shape and initial rise methods but less so with results from variable heating rate method
On the correlation between annealing and variabilities in pulsed-luminescence from quartz
Get PDFProperties of luminescence lifetimes in quartz related to annealing between 500 and 900ºC have been investigated. The luminescence was pulse-stimulated at 470 nm from sets of granular quartz annealed at 500, 600, 700, 800, and 900ºC. The lifetimes decrease with annealing temperature from about 42 to 33 µѕ when the annealing temperature is increased from 500 to 900ºC. Luminescence lifetimes are most sensitive to duration of annealing at 600ºC, decreasing from 40.2 ± 0.7 µѕ by as much as 7 µѕ when the duration of annealing is changed from 10 to 60 min. However, at 800–900ºC lifetimes are essentially independent of annealing temperature at about 33 µѕ. Increasing the exciting beta dose causes an increase in the lifetimes of the stimulated luminescence in the sample annealed at 800ºC but not in those annealed at either 500 or 600ºC. The temperature-resolved distribution of luminescence lifetimes is affected by thermal quenching of luminescence. These features may be accounted for with reference to two principal luminescence centres involved in the luminescence emission process
A study of the kinetics of a high temperature thermoluminescence peak in annealed natural quartz
No full textThermoluminescence of a high temperature secondary glow-peak in natural quartz annealed at 900 °C is reported. The glow-curve of a sample irradiated to 10 Gy and measured at 1 °C/s shows three peaks; the main peak at 71 °C and two other weaker-intensity peaks at 125 °C and 177 °C. For reference, the peaks are labelled as I, II and III. This study is concerned with the secondary peak at 177 °C (peak III). The electron trap responsible for peak III is stable at ambient temperature as determined by monitoring the peak intensity after various delays between irradiation and measurement. The activation energy and frequency factor of the peak were estimated as ~1.24 eV and ~10¹² s⁻¹ respectively. The dose response of the peak in the range 1–300 Gy is sublinear. The influence of either partial heating or irradiation dose on the peak position suggest that the peak follows non-first-order kinetics
Temperature-dependence of time-resolved optically stimulated luminescence and composition heterogeneity of synthetic α-Al2O3: C
No full textThe relationship of pulse-width, lifetime and measurement temperature in describing intensity of time-resolved luminescence optically stimulated at 470 nm from α-Al2O3:C is reported. The change of luminescence intensity with stimulation temperature is discussed in terms of the signal integrated over a complete time-resolved luminescence spectrum or in terms of ratios of the signal emitted either during or after pulsed stimulation to the total signal obtained per spectrum. The temperature-induced change in these parameters depends on whether the pulse-width is less or more than the luminescence lifetime. This is because the lifetime in α-Al2O3:C varies with measurement temperature. We have developed and applied new models to distinguish thermal assistance from different traps and to use this information as an additional means to analyse thermal quenching by using the luminescence intensity integrated from time-resolved spectra. Using a model based on use of the throughput, the activation energy for thermal assistance was determined for the shallow trap as 0.054±0.001 eV and as 0.53±0.03 eV for the main trap. The activation energy for thermal quenching was then evaluated using luminescence yield during the pulse as 1.09±0.01 eV and as 1.12±0.01 eV using the throughput after the pulse. Using the new analytical method based on integrated intensity, the activation energy for thermal quenching was found as 1.00±0.07 eV. These values are self-consistent and show that the methods for analyzing temperature-induced changes in intensity and the attendant thermal effects, such as thermal assistance can be successfully applied. We have also reported a general mathematical model that accounts for the temperature-dependence of time-resolved luminescence from α-Al2O3:C. The luminescence study was complemented by investigation of the phase and composition heterogeneity of the samples
Thermoluminescence of K-Mg-Al-Zn fluorophosphate glass
No full textThe thermoluminescence of beta irradiated K-Mg-Al-Zn fluorophosphate glass is reported. A glow-curve corresponding to 10 Gy measured at 1 °C/s shows two peaks, a weaker-intensity one at 70 °C and a more prominent one at 235 °C, the subject of this report. The main peak was observed to fade with delay between irradiation and measurement and specifically, by 11% in 15 h. Its dose response is superlinear in the dose range 1–190 Gy although the change was linear for the initial 10 Gy. Regarding kinetic analysis, the activation energy of the higher temperature peak was evaluated as 1.31 eV and that of the lower temperature peak was found as 0.47 eV. It was also noted that the main peak is affected by thermal quenching with an activation energy for thermal quenching equal to 1.37 eV. It is proposed that the mechanism associated with the thermoluminescence in K-Mg-Al-Zn fluorophosphate glass is that electrons trapped by the metal cations are released during heating and then recombine with holes at oxygen sites
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