Optically stimulated luminescence and spectral emission features of radioluminescence and thermoluminescence of natural kunzite:
- Alatishe, M A, Ogundare, F O, Folley, Damilola E, Chithambo, Makaiko L, Chikwembani, S
- Authors: Alatishe, M A , Ogundare, F O , Folley, Damilola E , Chithambo, Makaiko L , Chikwembani, S
- Date: 2020
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/160478 , vital:40449 , https://doi.org/10.1016/j.radmeas.2020.106457
- Description: Features of luminescence optically stimulated from natural kunzite using 470 nm blue light are reported. Preparatory measurements of its X-ray excited radioluminescence and thermoluminescence show that the sample has two main bands centered at 360 nm and 600 nm. The optically stimulated luminescence discussed in this report was monitored in the UV region and is presumed to be the same 360 nm emission that appears in the radioluminescence and thermoluminescence spectra. The glow curve shows at least three peaks at 74, 202, 432 oC for heating at 1 oC and the third one is a composite of two. Only the first two peaks are deduced to contribute most of the optically stimulated luminescence.
- Full Text:
- Date Issued: 2020
- Authors: Alatishe, M A , Ogundare, F O , Folley, Damilola E , Chithambo, Makaiko L , Chikwembani, S
- Date: 2020
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/160478 , vital:40449 , https://doi.org/10.1016/j.radmeas.2020.106457
- Description: Features of luminescence optically stimulated from natural kunzite using 470 nm blue light are reported. Preparatory measurements of its X-ray excited radioluminescence and thermoluminescence show that the sample has two main bands centered at 360 nm and 600 nm. The optically stimulated luminescence discussed in this report was monitored in the UV region and is presumed to be the same 360 nm emission that appears in the radioluminescence and thermoluminescence spectra. The glow curve shows at least three peaks at 74, 202, 432 oC for heating at 1 oC and the third one is a composite of two. Only the first two peaks are deduced to contribute most of the optically stimulated luminescence.
- Full Text:
- Date Issued: 2020
Thermoluminescence of SrAl2O4: Eu2+, Dy3+: kinetic analysis of a composite-peak
- Chithambo, Makaiko L, Wako, A H, Finch, A A
- Authors: Chithambo, Makaiko L , Wako, A H , Finch, A A
- Date: 2017
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/124157 , vital:35571 , https://doi.org/10.1016/j.radmeas.2016.12.009
- Description: The kinetic analysis of thermoluminescence of beta-irradiated SrAl2O4:Eu2+,Dy3+ is reported. The glow-curve is dominated by an apparently-single peak. It has been demonstrated using a number of tests including partial dynamic-heating, isothermal heating, phosphorescence and, the effect of fading, that the peak and the glow-curve consists of a set of closely-spaced peaks. In view of the peak being complex, its first few components were abstracted and analysed and for comparison, the peak was also analysed assuming it is genuinely single.
- Full Text: false
- Date Issued: 2017
- Authors: Chithambo, Makaiko L , Wako, A H , Finch, A A
- Date: 2017
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/124157 , vital:35571 , https://doi.org/10.1016/j.radmeas.2016.12.009
- Description: The kinetic analysis of thermoluminescence of beta-irradiated SrAl2O4:Eu2+,Dy3+ is reported. The glow-curve is dominated by an apparently-single peak. It has been demonstrated using a number of tests including partial dynamic-heating, isothermal heating, phosphorescence and, the effect of fading, that the peak and the glow-curve consists of a set of closely-spaced peaks. In view of the peak being complex, its first few components were abstracted and analysed and for comparison, the peak was also analysed assuming it is genuinely single.
- Full Text: false
- Date Issued: 2017
Temperature-dependence of time-resolved optically stimulated luminescence and composition heterogeneity of synthetic α-Al2O3: C
- Chithambo, Makaiko L, Costin, G
- Authors: Chithambo, Makaiko L , Costin, G
- Date: 2017
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/124172 , vital:35573 , https://doi.org/10.1016/j.jlumin.2016.10.038
- Description: The 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.
- Full Text: false
- Date Issued: 2017
- Authors: Chithambo, Makaiko L , Costin, G
- Date: 2017
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/124172 , vital:35573 , https://doi.org/10.1016/j.jlumin.2016.10.038
- Description: The 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.
- Full Text: false
- Date Issued: 2017
Relative features of the principal and secondary luminescence lifetimes in quartz
- Chithambo, Makaiko L, Ogundare, F O
- Authors: Chithambo, Makaiko L , Ogundare, F O
- Date: 2017
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/125821 , vital:35820 , https://doi.10.1002/pssc.200673721
- Description: Quartz is a common natural mineral with properties that make it amenable for application in radiation dosimetry using luminescence methods [1]. The luminescence properties of quartz including its sensitivity and luminescence lifetimes undergo notable changes when the quartz is annealed, and in particular, near its phase inversion temperatures of 573 and 867 oC [2, 3]. The physical processes leading up to the emission of luminescence in quartz may be investigated using time-resolved optical stimulation. The aim of this method is to separate in time the stimulation and emission of luminescence to enable measurement of time-resolved luminescence spectra which may be resolved into associated lifetimes, defined in this sense as the delay between stimulation and emission of luminescence [4, 5]. A number of such studies show that annealing defines the detailed distribution of lifetimes with measurement temperature as well as the irradiation-dependent characteristics of the lifetimes [3, 6]. In particular, it was noted [3] that spectra measured at certain temperatures could be accurately resolved into more than one component, a scenario that pointed to the possibility of involvement of multiple luminescence centers in the emission of luminescence from quartz. The aim of this work is to build on the findings described, specifically to study the influence of measurement temperature and irradiation on the principal and subsidiary luminescence lifetimes in natural quartz.
- Full Text:
- Date Issued: 2017
- Authors: Chithambo, Makaiko L , Ogundare, F O
- Date: 2017
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/125821 , vital:35820 , https://doi.10.1002/pssc.200673721
- Description: Quartz is a common natural mineral with properties that make it amenable for application in radiation dosimetry using luminescence methods [1]. The luminescence properties of quartz including its sensitivity and luminescence lifetimes undergo notable changes when the quartz is annealed, and in particular, near its phase inversion temperatures of 573 and 867 oC [2, 3]. The physical processes leading up to the emission of luminescence in quartz may be investigated using time-resolved optical stimulation. The aim of this method is to separate in time the stimulation and emission of luminescence to enable measurement of time-resolved luminescence spectra which may be resolved into associated lifetimes, defined in this sense as the delay between stimulation and emission of luminescence [4, 5]. A number of such studies show that annealing defines the detailed distribution of lifetimes with measurement temperature as well as the irradiation-dependent characteristics of the lifetimes [3, 6]. In particular, it was noted [3] that spectra measured at certain temperatures could be accurately resolved into more than one component, a scenario that pointed to the possibility of involvement of multiple luminescence centers in the emission of luminescence from quartz. The aim of this work is to build on the findings described, specifically to study the influence of measurement temperature and irradiation on the principal and subsidiary luminescence lifetimes in natural quartz.
- Full Text:
- Date Issued: 2017
Time-resolved luminescence from quartz: an overview of contemporary developments and applications
- Chithambo, Makaiko L, Pagonis, Vasilis, Ankjærgaard, Christina
- Authors: Chithambo, Makaiko L , Pagonis, Vasilis , Ankjærgaard, Christina
- Date: 2016
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/124743 , vital:35658 , https://doi.org/10.1016/j.physb.2015.10.014
- Description: Time-resolved optical stimulation of luminescence has become established as a key method for measurement of optically stimulated luminescence from quartz, feldspar and α-Al2O3:C, all materials of interest in dosimetry. The aim of time-resolved optical stimulation is to separate in time the stimulation and emission of luminescence. The luminescence is stimulated from a sample using a brief light pulse and the emission monitored during stimulation in the presence of scattered stimulating light or after pulsing, over photomultiplier noise only. Although the use of the method in retrospective dosimetry has been somewhat limited, the technique has been successfully applied to study mechanisms in the processes leading up to luminescence emission. The main means for this has been the temperature dependence of the luminescence intensity as well as the luminescence lifetimes determined from time-resolved luminescence spectra. In this paper we review some key developments in theory and applications to quartz including methods of evaluating lifetimes, techniques of evaluating kinetic parameters using both the dependence of luminescence intensity and lifetime on measurement temperature, and of lifetimes on annealing temperature. We then provide an overview of some notable applications such as separation of quartz signals from a quartz–feldspar admixture and the utility of the dynamic throughput, a measure of luminescence measured as a function of the pulse width. The paper concludes with some suggestions of areas where further exploration would advance understanding of dynamics of luminescence in quartz and help address some outstanding problems in its application.
- Full Text: false
- Date Issued: 2016
- Authors: Chithambo, Makaiko L , Pagonis, Vasilis , Ankjærgaard, Christina
- Date: 2016
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/124743 , vital:35658 , https://doi.org/10.1016/j.physb.2015.10.014
- Description: Time-resolved optical stimulation of luminescence has become established as a key method for measurement of optically stimulated luminescence from quartz, feldspar and α-Al2O3:C, all materials of interest in dosimetry. The aim of time-resolved optical stimulation is to separate in time the stimulation and emission of luminescence. The luminescence is stimulated from a sample using a brief light pulse and the emission monitored during stimulation in the presence of scattered stimulating light or after pulsing, over photomultiplier noise only. Although the use of the method in retrospective dosimetry has been somewhat limited, the technique has been successfully applied to study mechanisms in the processes leading up to luminescence emission. The main means for this has been the temperature dependence of the luminescence intensity as well as the luminescence lifetimes determined from time-resolved luminescence spectra. In this paper we review some key developments in theory and applications to quartz including methods of evaluating lifetimes, techniques of evaluating kinetic parameters using both the dependence of luminescence intensity and lifetime on measurement temperature, and of lifetimes on annealing temperature. We then provide an overview of some notable applications such as separation of quartz signals from a quartz–feldspar admixture and the utility of the dynamic throughput, a measure of luminescence measured as a function of the pulse width. The paper concludes with some suggestions of areas where further exploration would advance understanding of dynamics of luminescence in quartz and help address some outstanding problems in its application.
- Full Text: false
- Date Issued: 2016
F-and F+-band radioluminescence and the influence of annealing on its emission spectra in Al2O3: C, Mg:
- Chithambo, Makaiko L, Kalita, Jitumani M, Finch, A A
- Authors: Chithambo, Makaiko L , Kalita, Jitumani M , Finch, A A
- Date: 2020
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/150130 , vital:38942 , https://doi.org/10.1016/j.radmeas.2020.106306
- Description: Radioluminescence spectra of Al2O3:C,Mg monitored at temperatures up to 400 °C is reported. Measurements were made on samples either as received or on ones annealed at 1200 °C. Radioluminescence is observed at 410 nm for the unannealed sample but principally at 330 and 410 nm in the annealed sample with the emission at 330 nm dominant. Both bands are subject to thermal quenching but the change for the F+ band is atypical. Temperature induced effects on these and other bands are discussed, as are complementary measurements of thermoluminescence spectra.
- Full Text:
- Date Issued: 2020
- Authors: Chithambo, Makaiko L , Kalita, Jitumani M , Finch, A A
- Date: 2020
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/150130 , vital:38942 , https://doi.org/10.1016/j.radmeas.2020.106306
- Description: Radioluminescence spectra of Al2O3:C,Mg monitored at temperatures up to 400 °C is reported. Measurements were made on samples either as received or on ones annealed at 1200 °C. Radioluminescence is observed at 410 nm for the unannealed sample but principally at 330 and 410 nm in the annealed sample with the emission at 330 nm dominant. Both bands are subject to thermal quenching but the change for the F+ band is atypical. Temperature induced effects on these and other bands are discussed, as are complementary measurements of thermoluminescence spectra.
- Full Text:
- Date Issued: 2020
Thermoluminescence of the main peak in SrAl2O4: Eu2+, Dy3+: spectral and kinetics features of secondary emission detected in the ultra-violet region
- Authors: Chithambo, Makaiko L
- Date: 2017
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/124197 , vital:35575 , https://doi.org/10.1016/j.radmeas.2016.12.001
- Description: We 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.
- Full Text: false
- Date Issued: 2017
- Authors: Chithambo, Makaiko L
- Date: 2017
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/124197 , vital:35575 , https://doi.org/10.1016/j.radmeas.2016.12.001
- Description: We 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.
- Full Text: false
- Date Issued: 2017
Phosphorescence of orthopaedic–grade ultra high molecular weight polyethylene
- Authors: Chithambo, Makaiko L
- Date: 2008
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/125617 , vital:35801 , https://doi.10.1002/pssc.200776802
- Description: Isothermal 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.
- Full Text:
- Date Issued: 2008
- Authors: Chithambo, Makaiko L
- Date: 2008
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/125617 , vital:35801 , https://doi.10.1002/pssc.200776802
- Description: Isothermal 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.
- Full Text:
- Date Issued: 2008
Time-resolved luminescence of low sensitivity quartz from crystalline rocks
- Chithambo, Makaiko L, Preusser, F, Ramseyer, K, Ogundare, F O
- Authors: Chithambo, Makaiko L , Preusser, F , Ramseyer, K , Ogundare, F O
- Date: 2007
- Language: English
- Type: text , article
- Identifier: vital:6801 , http://hdl.handle.net/10962/d1004164 , https://doi.org/10.1016/j.radmeas.2006.07.005
- Description: preprint , Time-resolved luminescence spectra of low sensitivity natural quartz from crystalline rocks are presented. The luminescence was pulse-stimulated at width using 470 nm blue light from quartz separated from plutonic, metamorphic, volcanic and hydrothermal samples. Measurements were made at 20 °C. All samples show evidence of a short lifetime component less than long although in several cases too weak in intensity to be evaluated accurately. On the other hand, the value of the principal lifetime component varies considerably being about in metamorphic quartz, in plutonic quartz, and in one example of hydrothermal quartz. The results illustrate a new feature of luminescence from quartz for which lifetimes less than or greater than have never been reported at room temperature before. It is argued that the thermal provenance of the quartz and so the annealing it will have experienced influences the size of the observed lifetime. In particular, the results are explained in terms of a model consisting of three luminescence centers with the dominant lifetime linked to preferential recombination at one center depending on the thermal history of the sample and hence the hole concentration of the center.
- Full Text:
- Date Issued: 2007
- Authors: Chithambo, Makaiko L , Preusser, F , Ramseyer, K , Ogundare, F O
- Date: 2007
- Language: English
- Type: text , article
- Identifier: vital:6801 , http://hdl.handle.net/10962/d1004164 , https://doi.org/10.1016/j.radmeas.2006.07.005
- Description: preprint , Time-resolved luminescence spectra of low sensitivity natural quartz from crystalline rocks are presented. The luminescence was pulse-stimulated at width using 470 nm blue light from quartz separated from plutonic, metamorphic, volcanic and hydrothermal samples. Measurements were made at 20 °C. All samples show evidence of a short lifetime component less than long although in several cases too weak in intensity to be evaluated accurately. On the other hand, the value of the principal lifetime component varies considerably being about in metamorphic quartz, in plutonic quartz, and in one example of hydrothermal quartz. The results illustrate a new feature of luminescence from quartz for which lifetimes less than or greater than have never been reported at room temperature before. It is argued that the thermal provenance of the quartz and so the annealing it will have experienced influences the size of the observed lifetime. In particular, the results are explained in terms of a model consisting of three luminescence centers with the dominant lifetime linked to preferential recombination at one center depending on the thermal history of the sample and hence the hole concentration of the center.
- Full Text:
- Date Issued: 2007
Phototransferred thermoluminescence of synthetic quartz: analysis of illumination-time response curves
- Chithambo, Makaiko L, Niyonzima, P, Kalita, Jitumani M
- Authors: Chithambo, Makaiko L , Niyonzima, P , Kalita, Jitumani M
- Date: 2018
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/111020 , vital:33364 , https://doi.org/10.1016/j.jlumin.2018.02.029
- Description: Phototransferred thermoluminescence (PTTL) induced in synthetic quartz by 470 nm blue light is reported. The glow curve measured at 5 °C/s up to 500 °C after irradiation to 100 Gy shows six peaks at 94, 116, 175, 212, 280 and 348 °C labelled I through VI and another one at 80 °C (labelled A1). PTTL is only observed for peaks A1 and I and is induced at peak A1 as long as peak III has been removed by preheating and at peak I after preheating to deplete peak VI. The inducement of PTTL even when all peaks have been removed points to deep electron traps in the quartz also acting as donors in addition to the putative ones below 500 °C. The PTTL intensity as a function of duration of illumination for A1 goes through a peak and decreases monotonically or to a stable value depending on the preheating temperature. The change of PTTL intensity as a function of illumination time is described using a set of coupled linear differential equations. The number of acceptors and donors in a particular system described in this way is influenced by the preheating temperature.
- Full Text: false
- Date Issued: 2018
- Authors: Chithambo, Makaiko L , Niyonzima, P , Kalita, Jitumani M
- Date: 2018
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/111020 , vital:33364 , https://doi.org/10.1016/j.jlumin.2018.02.029
- Description: Phototransferred thermoluminescence (PTTL) induced in synthetic quartz by 470 nm blue light is reported. The glow curve measured at 5 °C/s up to 500 °C after irradiation to 100 Gy shows six peaks at 94, 116, 175, 212, 280 and 348 °C labelled I through VI and another one at 80 °C (labelled A1). PTTL is only observed for peaks A1 and I and is induced at peak A1 as long as peak III has been removed by preheating and at peak I after preheating to deplete peak VI. The inducement of PTTL even when all peaks have been removed points to deep electron traps in the quartz also acting as donors in addition to the putative ones below 500 °C. The PTTL intensity as a function of duration of illumination for A1 goes through a peak and decreases monotonically or to a stable value depending on the preheating temperature. The change of PTTL intensity as a function of illumination time is described using a set of coupled linear differential equations. The number of acceptors and donors in a particular system described in this way is influenced by the preheating temperature.
- Full Text: false
- Date Issued: 2018
Orthopaedic grade ultra–high molecular weight polyethylene: some features of the main thermoluminescence glow curve
- Authors: Chithambo, Makaiko L
- Date: 2006
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/125499 , vital:35789 , https://doi.10.1093/rpd/nci661
- Description: Thermoluminescence (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.
- Full Text:
- Date Issued: 2006
- Authors: Chithambo, Makaiko L
- Date: 2006
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/125499 , vital:35789 , https://doi.10.1093/rpd/nci661
- Description: Thermoluminescence (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.
- Full Text:
- Date Issued: 2006
Optically stimulated luminescence of ultra-high molecular weight polyethylene: a study of dosimetric features
- Chithambo, Makaiko L, Kalita, Jitumani M
- Authors: Chithambo, Makaiko L , Kalita, Jitumani M
- Date: 2018
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/110035 , vital:33217 , https://doi.org/10.1016/j.radmeas.2018.06.006
- Description: We report the dosimetric features of ultra-high molecular weight polyethylene (UHMWPE) using luminescence optically stimulated using 470 nm blue light. Samples irradiated to between 1 and 1000 Gy produces luminescence that increases with irradiation dose to produce a linear dose response between 1 and 1000 Gy. The sample was determined not to be affected by pre-dose in tests using a pre-dose of 4000 Gy. This characteristic precludes the need for elaborate background erasing routines typical of dosimetry experiments. The signal has good reproducibility. We used this property to test recovery of ‘unknown’ doses with encouraging results. It was observed that luminescence can also be stimulated using 870 nm infrared light. The dose response, fading, pre-dose effect and the ability to optically stimulate luminescence from the polymer is discussed in terms of curing involving free-radicals.
- Full Text: false
- Date Issued: 2018
- Authors: Chithambo, Makaiko L , Kalita, Jitumani M
- Date: 2018
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/110035 , vital:33217 , https://doi.org/10.1016/j.radmeas.2018.06.006
- Description: We report the dosimetric features of ultra-high molecular weight polyethylene (UHMWPE) using luminescence optically stimulated using 470 nm blue light. Samples irradiated to between 1 and 1000 Gy produces luminescence that increases with irradiation dose to produce a linear dose response between 1 and 1000 Gy. The sample was determined not to be affected by pre-dose in tests using a pre-dose of 4000 Gy. This characteristic precludes the need for elaborate background erasing routines typical of dosimetry experiments. The signal has good reproducibility. We used this property to test recovery of ‘unknown’ doses with encouraging results. It was observed that luminescence can also be stimulated using 870 nm infrared light. The dose response, fading, pre-dose effect and the ability to optically stimulate luminescence from the polymer is discussed in terms of curing involving free-radicals.
- Full Text: false
- Date Issued: 2018
Phototransferred thermoluminescence of α-Al2O3: C: experimental results and empirical models
- Chithambo, Makaiko L, Seneza, Cleophace, Kalita, Jitumani M
- Authors: Chithambo, Makaiko L , Seneza, Cleophace , Kalita, Jitumani M
- Date: 2017
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/115681 , vital:34215 , https://doi.org/10.1016/j.radmeas.2017.08.009
- Description: The thermoluminescence glow curve of α-Al2O3:C consists of a prominent apparently-single peak and a number of weaker intensity secondary peaks. Phototransferred thermoluminescence (PTTL) from secondary glow peaks in α-Al2O3:C is reported. For completeness and to aid discussion, complementary results for the main peak are included. The problem studied is one of phototransferred thermoluminescence for a system of multiple acceptors and multiple donors. A TL glow curve recorded at 5 °C/s following irradiation to 0.5 Gy shows the main peak (labelled II) at 240 °C and two secondary peaks at 86 °C (peak I) and 360 °C (peak III). Peak I is reproduced under phototransfer after any preheating between 100 and 500 °C. Peak II is also reproduced as a PTTL peak after preheating to any temperature up to 800 °C. For the latter, the duration of preheating matters because if the sample is preheated at 800 °C for say, 6 min, PTTL is obtained but not when this is extended to say, 15 min. No PTTL was observed from peak III at all. A study of the time dependence of the PTTL intensity from peak III, following preheating that removes peaks I and II, shows that its electron trap acts as an acceptor when the duration of illumination to stimulate electrons from deep traps is brief but that when the illumination time is extended, the electron trap for peak III loses some of its trapped electrons to the shallower traps thus acting as a donor trap.
- Full Text: false
- Date Issued: 2017
- Authors: Chithambo, Makaiko L , Seneza, Cleophace , Kalita, Jitumani M
- Date: 2017
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/115681 , vital:34215 , https://doi.org/10.1016/j.radmeas.2017.08.009
- Description: The thermoluminescence glow curve of α-Al2O3:C consists of a prominent apparently-single peak and a number of weaker intensity secondary peaks. Phototransferred thermoluminescence (PTTL) from secondary glow peaks in α-Al2O3:C is reported. For completeness and to aid discussion, complementary results for the main peak are included. The problem studied is one of phototransferred thermoluminescence for a system of multiple acceptors and multiple donors. A TL glow curve recorded at 5 °C/s following irradiation to 0.5 Gy shows the main peak (labelled II) at 240 °C and two secondary peaks at 86 °C (peak I) and 360 °C (peak III). Peak I is reproduced under phototransfer after any preheating between 100 and 500 °C. Peak II is also reproduced as a PTTL peak after preheating to any temperature up to 800 °C. For the latter, the duration of preheating matters because if the sample is preheated at 800 °C for say, 6 min, PTTL is obtained but not when this is extended to say, 15 min. No PTTL was observed from peak III at all. A study of the time dependence of the PTTL intensity from peak III, following preheating that removes peaks I and II, shows that its electron trap acts as an acceptor when the duration of illumination to stimulate electrons from deep traps is brief but that when the illumination time is extended, the electron trap for peak III loses some of its trapped electrons to the shallower traps thus acting as a donor trap.
- Full Text: false
- Date Issued: 2017
Radioluminescence of annealed synthetic quartz
- Chithambo, Makaiko L, Niyonzima, P
- Authors: Chithambo, Makaiko L , Niyonzima, P
- Date: 2017
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/115504 , vital:34150 , https://doi.org/10.1016/j.radmeas.2017.02.005
- Description: The radioluminescence of synthetic quartz annealed at various temperatures up to 1000 °C is reported. The amplitude of the emission bands increases with annealing temperature. In addition, when samples are annealed at temperatures exceeding 700 °C, the intensity of the radioluminescence increases with duration of annealing. The corresponding emission spectra show seven emission bands at 2.04, 2.54, 2.77, 3.04, 3.40, 3.75 and 3.91 eV. The change in dominant emission band with annealing is consistent with annealing-induced variations in lifetimes determined previously from time-resolved optically stimulated luminescence spectra in the same samples.
- Full Text: false
- Date Issued: 2017
- Authors: Chithambo, Makaiko L , Niyonzima, P
- Date: 2017
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/115504 , vital:34150 , https://doi.org/10.1016/j.radmeas.2017.02.005
- Description: The radioluminescence of synthetic quartz annealed at various temperatures up to 1000 °C is reported. The amplitude of the emission bands increases with annealing temperature. In addition, when samples are annealed at temperatures exceeding 700 °C, the intensity of the radioluminescence increases with duration of annealing. The corresponding emission spectra show seven emission bands at 2.04, 2.54, 2.77, 3.04, 3.40, 3.75 and 3.91 eV. The change in dominant emission band with annealing is consistent with annealing-induced variations in lifetimes determined previously from time-resolved optically stimulated luminescence spectra in the same samples.
- Full Text: false
- Date Issued: 2017
Thermoluminescence of annealed synthetic quartz: the influence of annealing on kinetic parameters and thermal quenching
- Dawam, Robert R, Chithambo, Makaiko L
- Authors: Dawam, Robert R , Chithambo, Makaiko L
- Date: 2018
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/110050 , vital:33218 , https://doi.org/10.1016/j.radmeas.2018.06.004
- Description: The thermoluminescence of synthetic quartz annealed at various temperatures up to 900 °C is reported. Glow curves measured at 1 oCs−1 following beta irradiation to 40 Gy from a sample annealed at 500 °C and from an unannealed one consist of a prominent peak at 70 °C and secondary peaks at 110, 180 and 310 °C. In comparison, the glow peak from the sample annealed at 900 °C consists of three peaks but with the main peak at 86 °C and other lower intensity peaks at 170 and 310 °C. Kinetic analysis was carried out on the main peak only in each case. The order of kinetics of this peak was determined to be first order using various methods. The activation energy was evaluated as an average of 0.90±0.02eV for the unannealed sample and the one annealed at 500 °C. However, when the synthetic quartz is annealed at 900 °C, the activation energy decreases to 0.65±0.02eV. The main point of interest however concerns thermal quenching. It was noted that for the sample annealed at 500 °C as well as the unannealed one, the maximum intensity of the main peak decreases with heating rate. This phenomenon is associated with thermal quenching. When the same experiment is carried out using quartz annealed at 900 °C and irradiated to the same dose, namely 40 Gy, the intensity increases with heating rate. This would imply that this sample is not affected by thermal quenching. Using the notion that the radiative and non-radiative recombination routes are competitive, we repeated the experiment using a low dose of 3 Gy. In this case, the intensity decreased with heating rate showing that the process can be tuned. The activation energy for thermal quenching for the samples annealed at 900 °C, 500 °C and unnannealed one was found as 0.65±0.02eV, 0.82±0.02eV and 0.95±0.06eV. Evidently, annealing affects recombination processes in synthetic quartz.
- Full Text: false
- Date Issued: 2018
- Authors: Dawam, Robert R , Chithambo, Makaiko L
- Date: 2018
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/110050 , vital:33218 , https://doi.org/10.1016/j.radmeas.2018.06.004
- Description: The thermoluminescence of synthetic quartz annealed at various temperatures up to 900 °C is reported. Glow curves measured at 1 oCs−1 following beta irradiation to 40 Gy from a sample annealed at 500 °C and from an unannealed one consist of a prominent peak at 70 °C and secondary peaks at 110, 180 and 310 °C. In comparison, the glow peak from the sample annealed at 900 °C consists of three peaks but with the main peak at 86 °C and other lower intensity peaks at 170 and 310 °C. Kinetic analysis was carried out on the main peak only in each case. The order of kinetics of this peak was determined to be first order using various methods. The activation energy was evaluated as an average of 0.90±0.02eV for the unannealed sample and the one annealed at 500 °C. However, when the synthetic quartz is annealed at 900 °C, the activation energy decreases to 0.65±0.02eV. The main point of interest however concerns thermal quenching. It was noted that for the sample annealed at 500 °C as well as the unannealed one, the maximum intensity of the main peak decreases with heating rate. This phenomenon is associated with thermal quenching. When the same experiment is carried out using quartz annealed at 900 °C and irradiated to the same dose, namely 40 Gy, the intensity increases with heating rate. This would imply that this sample is not affected by thermal quenching. Using the notion that the radiative and non-radiative recombination routes are competitive, we repeated the experiment using a low dose of 3 Gy. In this case, the intensity decreased with heating rate showing that the process can be tuned. The activation energy for thermal quenching for the samples annealed at 900 °C, 500 °C and unnannealed one was found as 0.65±0.02eV, 0.82±0.02eV and 0.95±0.06eV. Evidently, annealing affects recombination processes in synthetic quartz.
- Full Text: false
- Date Issued: 2018
Influence of annealing on thermoluminescence of natural quartz: kinetic analysis and experimental study of apparent inverse thermal quenching
- Folley, Damilola E, Chithambo, Makaiko L
- Authors: Folley, Damilola E , Chithambo, Makaiko L
- Date: 2018
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/109996 , vital:33212 , https://doi.org/10.1016/j.radmeas.2018.04.010
- Description: The influence of annealing on the main thermoluminescence glow-peak of natural quartz is reported. For comparison, results from un-annealed quartz are included. The glow-curve measured at 1 °Cs−1 after beta irradiation to 50 Gy revealed six peaks each for quartz annealed at 800 °C for 1 h and the un-annealed sample. The main peak in both quartzes was observed at 72 °C. This report focusses on kinetic analysis of the main peak. The analysis was carried out using various methods consisting of the initial rise, whole glow-peak, peak shape, variable heating rate and phosphorescence-based methods. The activation energy obtained using the various methods ranges between and for the annealed sample and between and for the un-annealed sample. The result suggests that annealing has little effect on the activation energy. The luminescence intensity decreased with heating rate in the un-annealed sample in a manner suggestive of thermal quenching. In contrast, the dependence of intensity on heating rate in the annealed sample is influenced by the dose the sample is irradiated to. Whereas thermal quenching was noted for a dose of 50 Gy in the un-annealed sample, the annealed sample showed evidence of thermal quenching at a low dose of 3 Gy with the opposite effect when irradiated to 50 Gy. The activation energies of thermal quenching were found as and for the un-annealed and annealed samples respectively. We ascribe the apparent dependence of thermal quenching on dose in the annealed sample to competition between radiative and non-radiative transitions at the recombination centre.
- Full Text: false
- Date Issued: 2018
- Authors: Folley, Damilola E , Chithambo, Makaiko L
- Date: 2018
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/109996 , vital:33212 , https://doi.org/10.1016/j.radmeas.2018.04.010
- Description: The influence of annealing on the main thermoluminescence glow-peak of natural quartz is reported. For comparison, results from un-annealed quartz are included. The glow-curve measured at 1 °Cs−1 after beta irradiation to 50 Gy revealed six peaks each for quartz annealed at 800 °C for 1 h and the un-annealed sample. The main peak in both quartzes was observed at 72 °C. This report focusses on kinetic analysis of the main peak. The analysis was carried out using various methods consisting of the initial rise, whole glow-peak, peak shape, variable heating rate and phosphorescence-based methods. The activation energy obtained using the various methods ranges between and for the annealed sample and between and for the un-annealed sample. The result suggests that annealing has little effect on the activation energy. The luminescence intensity decreased with heating rate in the un-annealed sample in a manner suggestive of thermal quenching. In contrast, the dependence of intensity on heating rate in the annealed sample is influenced by the dose the sample is irradiated to. Whereas thermal quenching was noted for a dose of 50 Gy in the un-annealed sample, the annealed sample showed evidence of thermal quenching at a low dose of 3 Gy with the opposite effect when irradiated to 50 Gy. The activation energies of thermal quenching were found as and for the un-annealed and annealed samples respectively. We ascribe the apparent dependence of thermal quenching on dose in the annealed sample to competition between radiative and non-radiative transitions at the recombination centre.
- Full Text: false
- Date Issued: 2018
Phototransferred thermoluminescence and thermally-assisted optically stimulated luminescence dosimetry using α-Al2O3:C,Mg annealed at 1200°C
- Kalita, Jitumani M, Chithambo, Makaiko L
- Authors: Kalita, Jitumani M , Chithambo, Makaiko L
- Date: 2018
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/105422 , vital:32511 , https://doi.org/10.1016/j.jlumin.2018.08.085
- Description: We report phototransferred thermoluminescence (PTTL) and thermally-assisted optically stimulated luminescence (TA-OSL) of α-Al2O3:C,Mg annealed at 1200 °C. PTTL is TL measured from an irradiated phosphor after its exposure to light. The other theme of this study, TA-OSL is the additional amount of luminescence optically stimulated from a sample over and above the amount that would be measured at room temperature. A sample irradiated to 10 Gy and preheated to 230 °C at 1 °C/s followed by illumination by 470 nm blue light produced four PTTL peaks at 53, 80, 102 and 173 °C. The PTTL peaks occur at the same positions as the corresponding conventional TL peaks. Their kinetic parameters are also similar. The intensity of the PTTL peaks increased with duration of illumination to a maximum within 200 s for doses between 1 Gy and 10 Gy. The dose response of each of the PTTL peaks at 80, 102 and 173 °C is linear within 1–15 Gy. The rate of fading is low and the peaks are reproducible. When the irradiated sample is optically stimulated at temperatures between 30 °C and 300 °C, after preheating to 500 °C, the intensity of its TA-OSL goes through a peak with temperature at 200 °C. Using the rising edge of the plot, activation energy of thermal assistance for a deep electron trap was estimated as (0.21 ± 0.02) eV. The TA-OSL dose response is sublinear from 10–250 Gy and saturates thereafter. The PTTL and TA-OSL analyses signify that the concentration of deep traps in α-Al2O3:C,Mg increased after annealing at 1200 °C. As a result, the sample produced better PTTL and TA-OSL response than when annealed at lower temperature.
- Full Text: false
- Date Issued: 2018
- Authors: Kalita, Jitumani M , Chithambo, Makaiko L
- Date: 2018
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/105422 , vital:32511 , https://doi.org/10.1016/j.jlumin.2018.08.085
- Description: We report phototransferred thermoluminescence (PTTL) and thermally-assisted optically stimulated luminescence (TA-OSL) of α-Al2O3:C,Mg annealed at 1200 °C. PTTL is TL measured from an irradiated phosphor after its exposure to light. The other theme of this study, TA-OSL is the additional amount of luminescence optically stimulated from a sample over and above the amount that would be measured at room temperature. A sample irradiated to 10 Gy and preheated to 230 °C at 1 °C/s followed by illumination by 470 nm blue light produced four PTTL peaks at 53, 80, 102 and 173 °C. The PTTL peaks occur at the same positions as the corresponding conventional TL peaks. Their kinetic parameters are also similar. The intensity of the PTTL peaks increased with duration of illumination to a maximum within 200 s for doses between 1 Gy and 10 Gy. The dose response of each of the PTTL peaks at 80, 102 and 173 °C is linear within 1–15 Gy. The rate of fading is low and the peaks are reproducible. When the irradiated sample is optically stimulated at temperatures between 30 °C and 300 °C, after preheating to 500 °C, the intensity of its TA-OSL goes through a peak with temperature at 200 °C. Using the rising edge of the plot, activation energy of thermal assistance for a deep electron trap was estimated as (0.21 ± 0.02) eV. The TA-OSL dose response is sublinear from 10–250 Gy and saturates thereafter. The PTTL and TA-OSL analyses signify that the concentration of deep traps in α-Al2O3:C,Mg increased after annealing at 1200 °C. As a result, the sample produced better PTTL and TA-OSL response than when annealed at lower temperature.
- Full Text: false
- Date Issued: 2018
The effect of annealing and beta irradiation on thermoluminescence spectra of α-Al2O3: C, Mg
- Kalita, Jitumani M, Chithambo, Makaiko L
- Authors: Kalita, Jitumani M , Chithambo, Makaiko L
- Date: 2018
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/112875 , vital:33669 , https://doi.org/10.1016/j.jlumin.2017.12.036
- Description: The effect of annealing on thermoluminescence spectra of beta irradiated α-Al2O3:C,Mg has been studied. Measurements were made on an un-annealed sample and samples annealed at 600, 700 and 900 °C. A glow curve measured at 1 °C/s from samples irradiated to 1 Gy shows a high intensity peak at 163 °C and six secondary peaks of weaker intensity at 43, 73, 195, 280, 329 and 370 °C. When the samples are annealed at 700 or 900 °C, an additional secondary peak appears at 100 °C. The thermoluminescence spectrum of an un-annealed sample measured at 1 °C/s between 300 and 700 nm shows the main emission band at ~ 410 nm and subsidiary emission bands at ~ 325 and 485 nm. The emission from samples annealed at 700 and 900 °C show similar bands except for a decrease in intensity of the emission at 485 nm. The emission bands at 325, 410 and 485 nm are attributed to F+, F and F22+(2Mg) -centres respectively. The decrease of the emission band at 485 nm is deduced to be due to the destruction of the F22+(2Mg) centre at 700 °C. The emission bands are unaffected by irradiation dose between 10 and 320 Gy. However, when the sample is annealed at or beyond 700 °C, any effects on the F+ and F centres emission can be easier distinguished particularly for doses greater than 10 Gy.
- Full Text: false
- Date Issued: 2018
- Authors: Kalita, Jitumani M , Chithambo, Makaiko L
- Date: 2018
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/112875 , vital:33669 , https://doi.org/10.1016/j.jlumin.2017.12.036
- Description: The effect of annealing on thermoluminescence spectra of beta irradiated α-Al2O3:C,Mg has been studied. Measurements were made on an un-annealed sample and samples annealed at 600, 700 and 900 °C. A glow curve measured at 1 °C/s from samples irradiated to 1 Gy shows a high intensity peak at 163 °C and six secondary peaks of weaker intensity at 43, 73, 195, 280, 329 and 370 °C. When the samples are annealed at 700 or 900 °C, an additional secondary peak appears at 100 °C. The thermoluminescence spectrum of an un-annealed sample measured at 1 °C/s between 300 and 700 nm shows the main emission band at ~ 410 nm and subsidiary emission bands at ~ 325 and 485 nm. The emission from samples annealed at 700 and 900 °C show similar bands except for a decrease in intensity of the emission at 485 nm. The emission bands at 325, 410 and 485 nm are attributed to F+, F and F22+(2Mg) -centres respectively. The decrease of the emission band at 485 nm is deduced to be due to the destruction of the F22+(2Mg) centre at 700 °C. The emission bands are unaffected by irradiation dose between 10 and 320 Gy. However, when the sample is annealed at or beyond 700 °C, any effects on the F+ and F centres emission can be easier distinguished particularly for doses greater than 10 Gy.
- Full Text: false
- Date Issued: 2018
Thermally and optically stimulated luminescence of natural red and blue corundum (Al2O3)
- Kalita, Jitumani M, Thomas, Sunil, Chithambo, Makaiko L
- Authors: Kalita, Jitumani M , Thomas, Sunil , Chithambo, Makaiko L
- Date: 2019
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/105177 , vital:32472 , https://doi.org/10.1016/j.jlumin.2018.09.058
- Description: We report the thermoluminescence (TL) and optically stimulated luminescence (OSL) of natural corundum (Al2O3) of two varieties; one red and the other blue. X-ray fluorescence spectroscopy of the samples show that the concentration of Al2O3 in the red corundum is 43.05% and 46.87% in the blue corundum. TL measurements carried out on un-annealed samples and samples annealed at 700 °C, 900 °C and 1200 °C show that the TL sensitivity increases with annealing. The sensitivity of the red corundum reaches a maximum after annealing at 900 °C whereas that of the blue corundum increases with annealing up to the maximum annealing temperature of 1200 °C used in this study. Both samples have a complex glow curve between 30 °C and 500 °C. The composite nature of the glow curves is deduced to be due to a continuum in the trap distribution in the crystal. The activation energy of the traps vary between 0.70 eV and 1.15 eV. The dose response of the red corundum under TL is linear within 100‒1000 Gy whereas that of the blue corundum is superlinear for the same dose range. The TL of both samples is reproducible but the signal fades with time between irradiation and measurement. Both samples produce OSL under 470 nm blue light stimulation. The dose response of the OSL is superlinear within 100‒1000 Gy. It is found that the samples also produce thermally-assisted OSL (TA-OSL) at elevated temperature. The TA-OSL intensity of the red corundum increases with dose up to 400 Gy and saturates thereafter. On the other hand, the intensity of the blue corundum increases consistently with dose from 100 Gy to 1000 Gy.
- Full Text: false
- Date Issued: 2019
- Authors: Kalita, Jitumani M , Thomas, Sunil , Chithambo, Makaiko L
- Date: 2019
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/105177 , vital:32472 , https://doi.org/10.1016/j.jlumin.2018.09.058
- Description: We report the thermoluminescence (TL) and optically stimulated luminescence (OSL) of natural corundum (Al2O3) of two varieties; one red and the other blue. X-ray fluorescence spectroscopy of the samples show that the concentration of Al2O3 in the red corundum is 43.05% and 46.87% in the blue corundum. TL measurements carried out on un-annealed samples and samples annealed at 700 °C, 900 °C and 1200 °C show that the TL sensitivity increases with annealing. The sensitivity of the red corundum reaches a maximum after annealing at 900 °C whereas that of the blue corundum increases with annealing up to the maximum annealing temperature of 1200 °C used in this study. Both samples have a complex glow curve between 30 °C and 500 °C. The composite nature of the glow curves is deduced to be due to a continuum in the trap distribution in the crystal. The activation energy of the traps vary between 0.70 eV and 1.15 eV. The dose response of the red corundum under TL is linear within 100‒1000 Gy whereas that of the blue corundum is superlinear for the same dose range. The TL of both samples is reproducible but the signal fades with time between irradiation and measurement. Both samples produce OSL under 470 nm blue light stimulation. The dose response of the OSL is superlinear within 100‒1000 Gy. It is found that the samples also produce thermally-assisted OSL (TA-OSL) at elevated temperature. The TA-OSL intensity of the red corundum increases with dose up to 400 Gy and saturates thereafter. On the other hand, the intensity of the blue corundum increases consistently with dose from 100 Gy to 1000 Gy.
- Full Text: false
- Date Issued: 2019
Comprehensive kinetic analysis of thermoluminescence peaks of α-Al2O3: C, Mg
- Kalita, Jitumani M, Chithambo, Makaiko L
- Authors: Kalita, Jitumani M , Chithambo, Makaiko L
- Date: 2017
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/116142 , vital:34323 , https://doi.org/10.1016/j.jlumin.2017.01.003
- Description: A comprehensive kinetic analysis of the glow peaks in α-Al2O3:C,Mg is reported. A thermoluminescence glow curve measured at 1 °C/s after beta irradiation to 1 Gy shows a high intensity peak hereafter referred to as the main peak at 161 °C and six lower intensity secondary peaks at 42, 72, 193, 279, 330, 370 °C respectively. For ease of reference, the secondary peaks are labelled as I, II, IV, V, VI and VII respectively and the main peak denoted peak III. Kinetic analysis of the glow peaks has been carried out using the initial rise, whole glow peak, peak shape, variable heating rate and glow curve deconvolution methods as well as by way of phosphorescence. Using Tm-Tstop, Tm-dose and phosphorescence analyses, the order of kinetics of the peaks has been evaluated as first order. Analysis by the peak shape, whole glow peak and deconvolution methods produce the same conclusion. The activation energy of peaks I through VII are calculated as ~0.83, 0.96, 1.37, 1.20, 1.15, 1.61 and 1.94 eV respectively. The frequency factors for all the peaks are of the order of 109 to 1014 s−1. The question of thermal quenching affecting the peaks was considered. The peaks III, IV and V, the only ones that could be conveniently studied in this regard, were found to be affected by thermal quenching. The activation energy for thermal quenching was calculated for peak III as 0.96±0.03 eV, for peak VI as 0.95±0.07 eV and for peak V as 1.26±0.08 eV. The thermal quenching phenomenon has been discussed with reference to F+ and F centres. An energy band model has been developed to discuss the luminescence mechanisms in α-Al2O3:C,Mg in light of finding in this work.
- Full Text: false
- Date Issued: 2017
- Authors: Kalita, Jitumani M , Chithambo, Makaiko L
- Date: 2017
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/116142 , vital:34323 , https://doi.org/10.1016/j.jlumin.2017.01.003
- Description: A comprehensive kinetic analysis of the glow peaks in α-Al2O3:C,Mg is reported. A thermoluminescence glow curve measured at 1 °C/s after beta irradiation to 1 Gy shows a high intensity peak hereafter referred to as the main peak at 161 °C and six lower intensity secondary peaks at 42, 72, 193, 279, 330, 370 °C respectively. For ease of reference, the secondary peaks are labelled as I, II, IV, V, VI and VII respectively and the main peak denoted peak III. Kinetic analysis of the glow peaks has been carried out using the initial rise, whole glow peak, peak shape, variable heating rate and glow curve deconvolution methods as well as by way of phosphorescence. Using Tm-Tstop, Tm-dose and phosphorescence analyses, the order of kinetics of the peaks has been evaluated as first order. Analysis by the peak shape, whole glow peak and deconvolution methods produce the same conclusion. The activation energy of peaks I through VII are calculated as ~0.83, 0.96, 1.37, 1.20, 1.15, 1.61 and 1.94 eV respectively. The frequency factors for all the peaks are of the order of 109 to 1014 s−1. The question of thermal quenching affecting the peaks was considered. The peaks III, IV and V, the only ones that could be conveniently studied in this regard, were found to be affected by thermal quenching. The activation energy for thermal quenching was calculated for peak III as 0.96±0.03 eV, for peak VI as 0.95±0.07 eV and for peak V as 1.26±0.08 eV. The thermal quenching phenomenon has been discussed with reference to F+ and F centres. An energy band model has been developed to discuss the luminescence mechanisms in α-Al2O3:C,Mg in light of finding in this work.
- Full Text: false
- Date Issued: 2017