pH-Metric study of gamma-irradiated table sugar for dosimetry purpose

Table sugar has been studied for a long time as a dosimeter in radiation accident and in high-dose dosimetry by using different analytical techniques especially electron paramagnetic resonance (EPR) and optical absorption spectrometry (OA). In this work, we report the results obtained by pH-metry on gamma-irradiated sugar. Table sugar samples were exposed to gamma radiation with doses of 0.1–58 kGy. Aqueous solutions of sugar were prepared with different concentrations ranged from 1% to 60% (w/w). It was found that sugar solutions showed strong decrease of pH up to concentration of 10% (w/w) followed by a slow decrease for the concentrations between 10 and 60% (w/w). Two possible mechanisms are proposed to explain the acidity increasing of the sugar solutions based on the existence of a carbonyl radical induced by gamma irradiation in solid table sugar with an open ring structure. Results for radiation response, post-irradiation change, reading temperature, dose-rate effect and repeatability are presented in this study. The results showed that pH-metric/sugar solution is an adequate high-dose dosimetric system in the dose range of 0.1–10 kGy.     

Identification of irradiated rice noodles by electron spin resonance spectroscopy

Electron spin resonance (ESR) spectroscopy has been applied to the identification of the irradiation of a wide variety of foods. In this study, ESR was applied to identify irradiated rice noodles. A detailed ESR investigation of irradiated noodles was carried out in the dose range 0.5–3 kGy. The stability of the radiation-induced ESR signal at cold (?4 °C) and room (25 °C) temperatures was studied over a storage period of 24 weeks. Irradiated rice noodle samples exhibited a strong, symmetric doublet ESR signal centered at g = 2.0, whereas unirradiated noodle exhibited a very weak signal. The ESR signal intensity increased linearly with radiation dose ranging from 0.5 to 3 kGy. Keeping the samples at ?4 °C and 25 °C for 24 weeks caused decreases of 50% and 90% in the ESR signal intensities, respectively. However, long-term decay data at room temperature showed that the ESR technique could be used to identify irradiated rice noodles up to 24 weeks following irradiation.     

Development of dry polymer electrolyte based on polyethylene oxide with co-bridging agent crosslinked by electron beam

Polyethylene oxide (PEO)-based electrolytes were crosslinked using electron beam (EB) irradiation. The gel contents of a polymer film were increased after irradiation doses of 0, 140, 280, and 420 kGy, with ionic conductivities of 0.831, 1.55, 6.08, and 7.95 (× 10^? 5) S cm^? 1 at 40 °C, respectively. The slight decrease in conductivity at higher temperatures after irradiation is due to the retardation of polymer motion by crosslinking. The electrolyte with higher EB dose amount exhibits higher conductivity due to stabilization of the amorphous state. The EB crosslinking with a co-bridging agent shows enhanced conductivities of 4.71, 6.59, and 7.18 (× 10^? 5) S cm^? 1 at 40 °C, after irradiation with 140, 280, and 420 kGy. Addition of the co-bridging agent is effective for developing a crosslinked structure with a smaller EB dose. Tensile strength becomes two to three times higher with irradiation compared to the non-treated polymer. Combination of the EB technique with a co-bridging agent is a simple and effective method to prepare strong dry polymer electrolyte films with improved room temperature conductivity.     

TL and EPR studies of CaSO4:Dy phosphor to investigate its efficacy in measurement of food irradiation dose at sub-ambient temperatures

The effects of sub-ambient temperatures of irradiation and dose response of CaSO₄:Dy phosphor was investigated. The irradiation dose in the range 0.5–7.0 kGy was chosen to meet the requirement of commercial food irradiation at low temperature. Commercially available phosphor showed no significant change in glow curve structure with low temperature of irradiation. In order to enhance the sensitivity of the low temperature glow peak (142 °C), the phosphor was subjected to different post-preparation thermal treatments at 700–900 °C. The change in glows and improvement in dose response characteristics were explained by Electron Paramagnetic Resonance (EPR) spectroscopy. At sub-ambient temperature of irradiation, the behavior of thermally treated CaSO₄:Dy phosphor with increasing dose revealed improved linear response of the low temperature glow peak and could be an efficient dosimetry system for the food commodities irradiated at low temperatures.     

Radiation effect studies on some glycine derivatives in solid state

Five glycyl derivatives, glycyl-L-histidine, L-alanyl-glycine, glycine hydrochloride, gly-gly hydrochloride and, gly-gly-glycine in powder form were exposed to 20?kGy doses of ⁶⁰Co gamma radiation to study the effects of ionizing radiation. In these compounds, the paramagnetic centers formed after irradiation were attributed to the R─NHCH─?O^?OH, ?H₂CHNH, H₂NCH₂?O^?OHHCl, NH₂?HCONHCH₂COOHHCl and HNCH₂?O^?OH radicals, respectively. The effect of gamma irradiation to the radical structures and time stability of the radicals were investigated by EPR spectroscopy. The spectra were computer simulated and the hyperfine coupling constants were determined.     

A radiochromic film based on leucomalachite green for high-dose dosimetry applications

A colorless polyvinyl butyral film (PVB) based on radiation-sensitive dye of leucomalachite green (LMG) was investigated as a high-dose dosimeter for gamma radiation processing applications in the dose range of 3–150 kGy. The useful applications for such dose range are food irradiation treatment, medical devices sterilization and polymer modification. Gamma irradiation of the film induces a significant intensity of green color, which can be characterized by a main absorption band at 627 nm and a small band at 425 nm. The variation in response of irradiated film stored in the dark and under laboratory light illumination was less than 3% during the first 6 days of storage. The response of film during irradiation was slightly influenced by relative humidity in the range of 12–76%; however, it was significantly affected by temperature in the range of 5–40 °C. The radiation chemical yield was reported to be 6.76 × 10⁻⁶ mol/J at the absorbed dose of 30 kGy for the film containing 6.5% of LMG dye. The overall uncertainty associated with routine dose monitoring would be less than 6% at a 95% confidence level if the dosimeter was being corrected for irradiation conditions and being calibrated with reference standard dosimeter in the production facility.     

EPR and UV spectroscopic investigations of sucrose irradiated with heavy-ion particles

Crystalline sucrose irradiated with C and Si ions is investigated with EPR and UV spectroscopy. Samples are treated at different doses of radiation in the region 20–300 Gy and linear energy transfer (LET) values of 39.6, 49 and 58 keV μm^?1 for C ions and 60 keV μm^?1 for Si ions. All samples exhibit identical EPR spectra due to radiation-induced stable sucrose radicals. At given constant LET the EPR signal responses are linear to the absorbed doses of Si and C ions. Water solutions of irradiated sucrose exhibit UV absorption maximum at 267 nm due to the product of radical recombination. The intensity of this band is stronger at irradiation with Si than with C ions. UV absorption is more sensitive to heavy-ion species irradiation than the EPR signals.     

Luminescence enhancement by gamma irradiation of nanocomposites for UV dosimetry devices

The aim of this work is to evaluate the influence of gamma radiation on a material constituted by a photonic complex used in a UV dosimetry device embedded in a polymeric composite with multiwalled carbon nanotubes (MWCNT). Films of CNT-free and MWCNT-containing composites were exposed to a gamma radiation beam of ⁶⁰Co. Characterization was performed by X-ray powder diffraction (XRD), thermogravimetric curves (TGA), and luminescence spectroscopy. The results indicate that the presented self-standing hybrid films show improvements to act as a better light conversion molecular device (LCMD) for UV dosimetry applications. Best results are attained after 50 kGy of gamma irradiation (⁶⁰Co) for CNT-free composites, and 5 kGy for MWCNT-containing films.     

Thermoluminescence,photoluminescence and EPR studies on Mn2+ activated yttrium aluminate (YAlO3) perovskite

Thermoluminescence (TL) measurements were carried out on undoped and Mn²⁺ doped (0.1 mol%) yttrium aluminate (YAlO₃) nanopowders using gamma irradiation in the dose range 1–5 kGy. These phosphors have been prepared at furnace temperatures as low as 400 °C by using the combustion route. Powder X-ray diffraction confirms the orthorhombic phase. SEM micrographs show that the powders are spherical in shape, porous with fused state and the size of the particles appeared to be in the range 50–150 nm. Electron Paramagnetic Resonance (EPR) studies reveal that Mn ions occupy the yttrium site and the valency of manganese remains as Mn²⁺. The photoluminescence spectrum shows a typical orange-to-red emission at 595 nm and suggests that Mn²⁺ ions are in strong crystalline environment. It is observed that TL intensity increases with gamma dose in both undoped and Mn doped samples. Four shouldered TL peaks at 126, 240, 288 and 350 °C along with relatively resolved glow peak at 180 °C were observed in undoped sample. However, the Mn doped samples show a shouldered peak at 115 °C along with two well defined peaks at ～215 and 275 °C. It is observed that TL glow peaks were shifted in Mn doped samples. The kinetic parameters namely activation energy (E), order of kinetics (b), frequency factor (s) of undoped, and Mn doped samples were determined at different gamma doses using the Chens glow peak shape method and the results are discussed in detail.     

Characterization of deep energy level defects in α-Al2O3:C using thermally assisted OSL

Commercially available α-Al₂O₃:C powder was studied for deep energy level defects by a newly suggested method using thermally assisted optically stimulated luminescence (TA-OSL) phenomenon. The method involves simultaneous application of continuous wave optically stimulated luminescence (CW-OSL) as well as thermal stimulation up to 400 °C, using a linear heating rate of 4 K/s. By using this method, two well-defined peaks at 121 °C and 232 °C were observed. These TA-OSL peaks have been correlated to two different types of deeper defects which can be bleached at 650 °C and 900 °C respectively on thermal treatment. These deeper defects, having larger thermal trap depth and relatively lower photoionization cross-section at room temperature for stimulation with blue LED (470 nm), are stable up to 500 °C, so they can store absorbed dose information even if the sample is inadvertently exposed to light or temperature. As only a fraction of signal is bleached during TA-OSL readout, multiple readouts could be performed on an exposed sample using this technique. The dose vs TA-OSL response from deep traps of α-Al₂O₃:C was found to be linear up to 10 kGy, thus extending its application for high dose dosimetry. The value of thermally assisted energy (E_A) associated with these traps in α-Al₂O₃:C has been determined to be 0.268 eV and 0.485 eV respectively and the corresponding values of photoionization cross-section at room temperature (25 °C), for optical stimulation with blue light (470 nm), are 5.82 × 10^?20 and 3.70 × 10^?22 cm², respectively. The process of thermally assisted OSL has been formulated analytically as well as theoretically for describing the temperature dependence of optical cross-section and evaluation of thermally assisted energy associated with deep traps.     

Influence of 60Co gamma irradiation on the structural and optical properties of 2-aminopyridinium 4-nitrophenolate 4-nitrophenol crystals

In this article, effect of gamma irradiation on the structural and optical properties of 2-aminopyridinium 4-nitrophenolate 4-nitrophenol (2AP4N) has been reported. The grown crystals of 2AP4N were exposed to ⁶⁰Co gamma rays with a dose of 50 kGy and 100 kGy. The radiation-induced effects were analyzed using X-ray diffraction, FT-IR, UV–visible, photoluminescence techniques. The refractive index was determined using a long arm spectrometer. The structural properties of the pristine and irradiated crystals were studied using powder XRD. The peak intensity decrease after irradiation may be attributed to the formation of point defects. The UV visible study reveals that the energy gap has decreased after irradiation and then has increased for the higher dose. The intensity variation in the PL spectra is due to colour center mechanism. The SHG efficiency of 2AP4N crystals was found to be unaffected by gamma irradiation.     

EPR dosimeter material properties of potassium tartrate hemihydrate

The ability of potassium tartrate hemihydrate as a radiation sensitive material for electron paramagnetic resonance (EPR) dosimetry was investigated. The samples were subjected to different doses, in the range of 1–9 Gy of ⁶⁰Co gamma rays at room temperature. The EPR spectra were investigated through variation of signal intensity with respect to absorbed dose, magnetic field modulation amplitude, microwave power and time stability. The results indicate that the sensitivity of potassium tartrate hemihydrate is about 30% higher than that of alanine. However, the EPR signal is timely less stable within the first two weeks after irradiation.     

Photostimulated luminescence of corrugated fiberboard as an additional screening method for detecting radiated foods

In this study, PSL of non-irradiated and irradiated corrugated fiberboards (CFs) was investigated to evaluate the possibility that CFs can be used as alternative specimens for the screening detection method of food irradiation. The irradiation at a dose of only 0.15 kGy increased PSL signals of the CF over 1 order of magnitude. The PSL signals increased with increasing in gamma irradiation dose and became almost saturated at a dose of 5 kGy. The core of CFs showed PSL signals sufficient for distinguishing irradiated from non-irradiated at least 6 months after irradiation even though the CF was exposed to light and the environmental temperature increased to 50 °C. These results suggest that the PSL property of the core of CFs is useful for detecting irradiation. However, the large variation of PSL signals among CFs made it difficult to set a well-defined “positive” threshold limit to distinguish irradiated from non-irradiated completely. All of the non-irradiated CFs showed PSL signals above 10³ counts, which is much higher than that detected for foods. It is apparent that the threshold limit of EN 13751 is not applicable to detecting irradiated CFs. More detailed collaborative research with large number of samples is needed to establish new threshold limits involving “intermediate” classification.     

Thermally stimulated transformation of the EPR spectra in γ-irradiated bone tissue

γ-irradiated bone tissue annealed at different temperatures is studied by EPR. In powder samples the annealing-induced changes of the EPR spectra are mainly determined by sharp growth of a signal caused by the products of thermal decay of an organic component in the tissue. This signal considerably complicates the analysis of the EPR spectrum shape for the annealed samples. On the other hand, in the spectra of the plates of bone tissue a change in the lineshape of the EPR signal from CO₂⁻ radicals after annealing is more pronounced than in powder, and it is attributed to the change in the contributions from axial and orthorhombic CO₂⁻ radicals. The analysis of different radicals concentrations vs. annealing temperature revealed above 210 °C the temperature-induced transformation of orthorhombic CO₂⁻ radicals into axial ones in bone tissue which (together with organic component) is responsible for the changes of EPR lineshape at annealing.     

Thermoluminescence response in gamma and UV irradiated Dy2O3 nanophosphor

Low temperature solution combustion method was employed to synthesize Dy₂O₃ nanophosphors using two different fuels (sugar and oxalyl dihydrazine (ODH)). Powder X-ray diffraction confirm pure cubic phase and the estimated particle size from Scherrer's method in sugar and ODH fuel was found to be 26 and 78 nm, respectively, and are in close agreement with those obtained using TEM and W–H plot analysis. SEM micrographs reveal porous, irregular shaped particles with large agglomeration in both the fuels. An optical band gap of 5.24 eV and 5.46 eV was observed for Dy₂O₃ for sugar and ODH fuels, respectively. The blueshift observed in sugar fuel is attributed to the particles size effect. Thermoluminescence (TL) response of cubic Dy₂O₃ nanophosphors prepared by both fuels was examined using gamma and UV radiations. The thermoluminescence of sugar used samples shows a single glow peak at 377 °C for 1–4 kGy gamma irradiations. When dose is increased to 5 kGy, two more shouldered peaks were observed at 245 and 310 °C. However, in TL of ODH used samples, a single glow peak at 376 °C was observed. It is observed that TL intensity is found to be more in sugar used samples. In UV irradiated samples a single glow peak at 365 °C was recorded in both the fuels with a little variation in TL intensity. The trapping parameters were estimated by different methods and the results are discussed.     

Egyptian limestone for gamma dosimetry: an electron paramagnetic resonance study

The electron paramagnetic resonance (EPR) properties of limestone from a certain Egyptian site were investigated in order to propose an efficient and low-cost gamma dosimeter. Radiation-induced free radicals were of one type which was produced in the limestone samples at g=2.0066 after exposure to gamma radiation (⁶⁰Co). EPR spectrum was recorded and analyzed. The microwave power saturation curve and the effect of changing modulation amplitude on peak-to- peak signal height were investigated. The response of limestone to different radiation doses (0.5–20 kGy) was studied. Except for the decrease in signal intensities during the first five hours following irradiation, over the period of two months fair stabilities of signal intensities were noticed. From the current results, it is possible to conclude that natural limestone may be a suitable material for radiation dosimetry in the range of irradiation processing.     

EPR and UV spectrometry investigation of sucrose irradiated with carbon particles

Solid state/EPR (SS/EPR) dosimeters of carbon ions irradiated sucrose are studied with EPR, and their water solutions – with UV spectroscopy. Doses between 20 and 200 Gy are used with linear energy transfer (LET) values for carbon ions of 63, 77, 96 and 230 keV μm^?1. After irradiation all samples show typical for irradiated sucrose EPR and UV spectra. The obtained data are compared with those previously reported for nitrogen particles and gamma rays irradiated sucrose. The identical shape of both the EPR and UV spectra of irradiated with various type radiation samples suggests that generated free radicals are not influenced by the nature of radiation. The lack of difference in the line width of the separate lines or the whole EPR spectrum, obtained for gamma and heavy particles irradiation, suggests negligible spin–spin interaction among the radiation-generated free radicals in the samples. The linear dependence of the EPR response on the absorbed dose radiation is found to be higher when generated by gamma rays, than by the same absorbed dose of heavy particles. In addition, the EPR response for carbon ions is higher than that for nitrogen ions. Water solutions of irradiated sucrose exhibit UV spectrum with absorption maximum at 267 nm, attributed to the recombination products of free radicals. The UV band intensity depends on the absorbed dose radiation. The UV spectra obtained for carbon, nitrogen and gamma rays irradiated sucrose are also compared.     

Defect induced paramagnetism in lightly doped ZnS:Fe nanoparticles

Nanoparticles of ZnS:Fe (0, 1, 3, and 5 at%) were synthesized by a refluxing route at 80 °C. All the samples exhibited cubic structure as revealed by X-ray powder diffraction studies. Blue emission of undoped samples was totally quenched by Fe doping. Magnetic measurements showed that the undoped ZnS was diamagnetic whereas all the doped samples were paramagnetic at room temperature. EPR signal characteristic of Fe³⁺ was observed in all the doped samples at room temperature. The paramagnetism of the present samples is attributed to the presence of uncoupled Fe³⁺ ions mediated by cation vacancies.     

Structural Properties of Cr<Superscript>3+</Superscript>-Doped Cadmium Oxide Nanopowders

The Cr³⁺-doped cadmium oxide nanopowder is prepared at room temperature by a mild and simple solution method. The prepared powder is characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), optical, electron paramagnetic resonance (EPR) and Fourier transform infrared (FT-IR) techniques. The XRD powder pattern reveals the lattice structure and cell parameters are evaluated. The SEM image shows the stone-like morphology of the nanopowder. The optical absorption spectrum indicates the distorted octahedral site symmetry of Cr³⁺ ions. The crystal field Dq and interelectronic repulsion parameters B and C are evaluated. The EPR spectrum gives a resonance signal at g = 1.973 for Cr³⁺ ions. The FT-IR spectrum reveals the characteristic vibrations of cadmium oxide.     

Synthesis,characterisation, luminescence and defect centres in solution combustion synthesised CaZrO3:Tb3+ phosphor

Tb³⁺ doped CaZrO₃ has been prepared by an easy solution combustion synthesis method. The combustion derived powder was investigated by X-ray diffraction, Fourier-transform infrared spectrometry and scanning electron microscopy techniques. A room temperature photoluminescence study showed that the phosphors can be efficiently excited by 251 nm light with a weak emission in the blue and orange region and a strong emission in green light region. CaZrO₃:Tb³⁺ exhibits three thermoluminescence (TL) glow peaks at 126 °C, 200 °C and 480 °C. Electron Spin Resonance (ESR) studies were carried out to study the defect centres induced in the phosphor by gamma irradiation and also to identify the centres responsible for the TL peaks. The room temperature ESR spectrum of irradiated phosphor appears to be a superposition of two distinct centres. One of the centres (centre I) with principal g-value 2.0233 is identified as an O^? ion. Centre II with an axial symmetric g-tensor with principal values g_=1.9986 and g_?=2.0023 is assigned to an F⁺ centre (singly ionised oxygen vacancy). An additional defect centre is observed during thermal annealing experiments and this centre (assigned to F⁺ centre) seems to originate from an F centre (oxygen vacancy with two electrons). The F centre and also the F⁺ centre appear to correlate with the observed high temperature TL peak in CaZrO₃:Tb³⁺ phosphor.