Optimization of the sensitivity and stability of the PRESAGE™ dosimeter using trihalomethane radical initiators

The aim of this study is to investigate the effect of trihalomethane radical initiators on the radiological properties, radiation dose sensitivity and post response photo-stability of the PRESAGE dosimeter. Different PRESAGE dosimeters containing 50 and 100 mM of iodoform (CHI₃), bromoform (CHBr₃) or chloroform (CHCl₃) radical initiators where fabricated and irradiated with 6 MV photons for a range of radiation doses from 0 to 30 Gy. A comparison between sensitivity and radiological properties of the PRESAGE dosimeters with the different radical initiators was carried out. Optical density changes of the dosimeters before and after irradiation were measured using a spectrophotometer. The incorporation of different radical initiators in the composition of the PRESAGE dosimeter resulted in variation of the radiation dose sensitivity and radiological properties of the dosimeters depending on the type and concentration of the radical initiator used, with iodoform showing the highest dose-response slope followed by bromoform and chloroform. However, at 100 mM iodoform, the effective atomic number was significantly higher than water (Z_eff=16). This enhancement in dose-response was found to be directly related to the carbon–halogen bond dissociation energy and to the radiological properties of each individual radical initiator used in this study. Furthermore, the post-response stability of the PRESAGE dosimeters over two weeks remained stable regardless of the trihalomethane radical initiator employed, with negligible change in the post-response stability and linearity of the PRESAGE dosimeters.     

Dyed polyvinyl chloride films for use as high-dose routine dosimeters in radiation processing

Characteristics of the polyvinyl chloride (PVC) films containing 0.11 wt% of malachite green oxalate or 6GX-setoglausine and about 100 μm in thickness were studied for use as routine dosimeters in radiation processing. These films show basically color bleaching under irradiation with ⁶⁰Co γ-rays in a dose range of 5–50 kGy. The sensitivity of the dosimeters and the linearity of dose-response curves are improved by adding 2.5% of chloral hydrate [CCl₃CH(OH)₂] and 0.15% hydroquinone [HOC₆H₄OH]. These additions extend the minimum dose limit to 1 kGy covering dosimetry requirements of the quality assurance in radiation processing of food and healthcare products. The dose responses of both dyed PVC films at irradiation temperatures from 20°C to 35°C are constant relative to those at 25°C, and the temperature coefficients for irradiation temperatures from 35°C to 55°C were estimated to be (0.43±0.01)%/°C. The dosimeter characteristics are stable within 1% at 25°C before and 60 days after the end of irradiation.     

Dμ—A new concept in industrial low-energy electron dosimetry

Irradiation with low-energy electrons (100–300 keV) results in dose gradients across the thickness of the dosimeters that are typically used for dose measurement at these energies. This leads to different doses being measured with different thickness dosimeters irradiated at the same electron beam, resulting in difficulties in providing traceable dose measurements using reference dosimeters. In order to overcome these problems a new concept is introduced of correcting all measured doses to the average dose in the first micrometer—D_μ. We have applied this concept to dose measurements with dosimeters of different thickness at two electron accelerators operating over a range of energies. The uncertainties of the dose measurements were evaluated, and it was shown that the dose in terms of D_μ was the same at each energy for all dosimeters within the measurement uncertainty. Using the concept of D_μ it is therefore possible to calibrate and measure doses from low-energy electron irradiations with measurement traceability to national standards.     

Selfcalibrated alanine/EPR dosimeters: A new generation of solid state/EPR dosimeters

Alanine/EPR dosimeters are well established as secondary, reference dosimeters for high-energy radiation. However, there are various sources of uncertainty in the evaluation of absorbed dose. This arises primarily from the necessity to calibrate each EPR spectrometer and each batch of dosimeters before their use. In order to overcome this disadvantage, a new generation alanine/EPR dosimeter has been developed, and its possibilities as a radiation detector are reported. Principally, it is a mixture of alanine, some quantity of EPR active substance, and a binding material. The EPR active substance, acting as an internal EPR standard, is chosen to have EPR parameters which are independent of the irradiation dose. The simultaneous recording of the spectra of both the sample and the standard under the same experimental conditions and the estimation of the ratioI _alanine/I _Mn as a function of the absorbed dose strongly reduces the uncertainties. The response of these dosimeters for⁶⁰Co γ-radiation exhibits excellent linearity and reproducibility in the range of absorbed dose, 10²−5·10⁴ Gy.     

Dosimetric calibration of an annular60Co gamma-ray source

Precise dosimetric calibration of the radiation field of the Gammacell irradiator has been carried out. For measuring spatial dose distribution a cavity ionization chamber in conjuction with a Farmer dosimeter and CaF₂ thermoluminescent dosimeters were used. The results make possible the calculation of doses received by samples of different sizes and shapes.     

Some Physico-Technical Aspects of the New Generation of Self-Calibrated Alanine/EPR Dosimeter and Results from the International Intercomparison trial

Some physico-technical parameters of the self-calibrated alanine/EPR dosimeters are described. Principally, this new type of solid state/EPR dosimeter contains radiation sensitive diamagnetic material (in the present case, alanine), some quantity of EPR active, but radiation insensitive, substance (for example, Mn²⁺/MgO) playing roles of an internal standard and a binding material. Thus with this dosimeter the EPR spectra of alanine and the internal standard Mn²⁺ are recorded simultaneously and the dose response is represented as a ratio of EPR signal intensities of alanine versus Mn²⁺ as a function of absorbed dose. As a result, the data of the present study have shown that there is practically no interference of the dosimeter EPR response (expressed as the ratio I _alanine/I _Mn) from the way of preparation (homogeneity), behavior after irradiation (fading of EPR signals with time, influence of different meteorological conditions) as well as specific spectrometer setting conditions. These dosimeters show satisfactory reproducibility of preparation and reading as well as stability on keeping. Thus, fulfilling the described physico-technical data of this type of dosimeters, the reproducibility of the readings is significantly improved particularly when intercomparison among different laboratories is performed. This conclusion is confirmed by independent studies of the described self-calibrated alanine/EPR dosimeters in several laboratories in Europe. Results of which are also reported.     

Modeling of Free‐radical Crosslinking Copolymerization of Acrylamide and N,N′‐Methylenebis(acrylamide) for Radiation Dosimetry

Over the past decade there has been much interest in the development of three‐dimensional gel dosimeters to aid in the determination of the distribution and magnitude of absorbed dose in clinical radiation therapy. A widely used dosimeter for verification of spatial dose distribution is the polyacrylamide system, sometimes termed polyacrylamide gel (PAG). In this paper, we develop a model to describe the kinetic mechanisms in this gel dosimeter, based on the radiation‐induced copolymerization of acrylamide and bisacrylamide monomers in water and gelatin. Using the proposed model, the conversion of both monomers and total vinyl groups, the concentrations of pendant double bonds (PDB), cyclized groups and crosslinks along the polymer chains as well as temperature changes were simulated. The model predictions and experimental findings in PAG dosimeters agree for a variety of recipes and spatially uniform radiation conditions. Further experiments are required to obtain accurate kinetic parameter estimates and to verify model predictions.

Comparison between the temperatures changes predicted by the model (dotted lines) and experimental data (solid lines) for PAGs irradiated to different doses.     

A New Manufacturing Process to Obtain Thermoluminescent Dosimeters Using Sol-Gel Method

A new manufacturing process using sol-gel method to obtain thermoluminescent dosimeters—TLDs is described. A LiF/SiO₂ thermoluminescent dosimeter in the form of reusable solid chip was prepared using an acid-catalyzed sol-gel process, with tetramethoxysilane (TMOS) and LiF powder as precursors. In comparison with the manufacturing process of typical lithium fluoride based dosimeters, the method optimizes the manufacturing process. The new dosimeter has a dose response over a dose range varying from 0.1 Gy to 160 Gy and can be used to detect higher doses using the typical commercial TLD readers without special adjustments. Furthermore, the process may be used for the preparation of other TLDs using a simple chemical processing.     

Three-dimensional polymer gel dosimetry: basic physical properties of the dosimeter

This study concentrated on assessment of the basic physical properties of a polymer gel dosimeter evaluated by NMR. For this, BANG-2 type polymer gel was prepared. The dosimeters were irradiated by ⁶⁰Co gamma photons and by 4, 6 and 18 MV X-ray photons for doses in the range 0–50 Gy. The multi-echo CPMG sequence was used for the evaluation of T₂-relaxation times in the irradiated gel dosimeters. Dependence of 1/T₂ in terms of the following factors was studied: absorbed dose, energy of applied radiation, temperature during NMR evaluation, time between irradiation and NMR evaluation and strength of the magnetic field. An exponential dependence of the 1/T₂ response on absorbed dose in the range 0–50 Gy was observed, while in the range 0–10 Gy the data could be fitted by a linear function. This paper also describes the dependence of 1/T₂ response on: radiation energy, strength of magnetic field and time from irradiation of the dosimeters to NMR evaluation. Increase of gel dosimeter 1/T₂ response with the decrease of the temperature during NMR evaluation has been qantitatively described. The polymer gel dosimetry system used in this study proved that it is a reliable system for three-dimensional dose distribution measurement.     

Optimizing the sensitivity and radiological properties of the PRESAGE® dosimeter using metal compounds

The aim of this study is to investigate the radiation-modifying effects of incorporating commercially available bismuth-, tin- and zinc-based compounds in the composition of the PRESAGE^® dosimeter, and the feasibility of employing such compounds for radiation dose enhancement. Furthermore, we demonstrate that metal compounds can be included in the formulation to yield water-equivalent PRESAGE^® dosimeters with enhanced dose response. Various concentrations of the metal compounds were added to a newly developed PRESAGE^® formulation and the resulting dosimeters were irradiated with 100 kV and 6 MV photon beams. A comparison between sensitivity and radiological properties of the PRESAGE^® dosimeters with and without the addition of metal compounds was carried out. Optical density changes of the dosimeters before and after irradiation were measured using a spectrophotometer. In general, when metal compounds were incorporated in the composition of the PRESAGE^® dosimeter, the sensitivity of the dosimeters to radiation dose increased depending on the type and concentration of the metal compound, with the bismuth compound showing the highest dose enhancement factor. In addition, these metal compounds were also shown to improve the retention of the post-response absorption value of the PRESAGE^® dosimeter over a period of 2 weeks. Thus, incorporating 1–3 mM (ca. 0.2 wt%) of any of the three investigated metal compounds in the composition of the PRESAGE^® dosimeter is found to be an efficient way to enhance the sensitivity of the dosimeter to radiation dose and stabilize its post-response for longer times. Furthermore, the addition of small amounts of the metal compounds also accelerates the polymerization of the PRESAGE^® dosimeter precursors, significantly reducing the fabrication time. Finally, a novel water-equivalent PRESAGE^® dosimeter formula optimized with metal compounds is proposed for clinical use in both kilovoltage and megavoltage radiotherapy dosimetry.     

Characterization of aqueous solution of cresol red as food irradiation dosimeter

Dilute aqueous solution of cresol red has been evaluated spectrophotometrically as possible gamma rays dosimeter. A 0.10 mM solution of cresol red was irradiated by gamma rays using a cobalt-60 radiation source. The absorbance spectra of the unirradiated and irradiated solutions were recorded using double beam scanning spectrophotometer. The absorbance of the solution before and after irradiation was measured at 434 nm (λ_max) as well as at other wavelengths (415, 448 and 470 nm). Various parameters, such as Absorbance (A), ΔA, %A, -log A and log A_o/A_i were plotted against radiation dose, in order to check the response of cresol red solution and its possible use as chemical dosimeter. The response plots of A, ΔA, and %A versus absorbed dose showed that the solution can be used as a radiation dosimeter in a dose range up to 0.82 kGy. Using response plots of -log A and log A_o/A_i, the useful dose range can be extended up to 1.65 kGy; which are useful dose ranges for food irradiation applications. Stability studies of cresol red solution at different light and temperature conditions for pre- and post-irradiated storage of the dosimetric solutions suggested that aqueous solution of cresol red is highly stable in dark, under fluorescence light and at room temperature up to 150 days     

Radiochromic dye dosimeter solutions as reference measurement systems

Solutions of leucocyanides of triphenylmethane dyes in organic solvents are designed as stable reference dosimeters for large radiation doses, with useful characteristics, both for steady-state and pulsed radiation fields. These radiochromic solutions may be used in conventional glass ampoules to cover the absorbed dose range 10²–10⁴kGy, when analyzed spectrophotometrically at visible wavelengths at the maxima of radiation-induced absorption bands. The radiation chemical yields of dye formation (G-values) and molar linear absorption coefficients (ϵ_m) of the dyes in several formulations, with and without dissolved polymer and weak oxidizing agents, are established. The most stable formulation before and after irradiation consists of new fuchsin cyanide in a mixture of dimethyl sulfoxide and triethyl phosphate containing small amounts of acetic acid, p-nitrobenzoic acid and polyvinyl butyral. The useful range of doses for this solution is 10²-4 x 10³ Gy when measured at 557 nm wavelength. The radiation chemical yield, G-value for dye production, is 3.35 x 10¹⁵ molec J^-1 (0.0055 μmol J^-1) and the value of ϵ_m at this wavelength is 1.32 x 10⁵ M^-1 cm^-1.     

A study on the role of gelatin in methacrylic-acid-based gel dosimeters

In radiotherapy treatment, polymer gel dosimetry can be used for verifying three-dimensional (3D) dose distributions. Gelatin is generally used as a gelling agent in the dosimeters. In this paper, another role of gelatin in a methacrylic-acid-based gel dosimeter (MAGAT) is investigated. Temperature increases due to exothermic polymerization in the irradiated gel are measured directly. Dose–R₂ responses are also obtained using MRI. It is shown that no appreciable increases in either temperature or R₂ are observed in MAGAT dosimeters made without gelatin, and that significant temperature and R₂ increases are observed when very low gelatin concentrations are used. These results indicate that gelatin is an important enabler for radiation-induced free-radical polymerization in methacrylic-acid-based gels. When gelatin is replaced by amino acids, changes in temperature are observed, along with small changes in R₂. The resulting dosimeter solutions remain transparent because the polymer does not precipitate as it does in regular MAGAT dosimeters containing gelatin. When the amino acids are replaced by acids without amino groups, no temperature or R₂ changes are observed, indicating that no polymer forms. These results show that amino groups (and possibly other functional groups) on the gelatin catalyze the radiation-induced free-radical polymerization that occurs in MAGAT dosimeters.     

Radiochromic film containing methyl viologen for radiation dosimetry

Poly(vinyl alcohol) (PVA) films containing methyl viologen (MV²⁺) that colours blue upon exposure to ionizing radiation were investigated as possible dosimeters for use in radiation processing applications. In order to find the most suitable composition of the PVA-MV²⁺ film, different concentrations of the dye have been studied. The absorbance values at selected wavelengths, obtained from irradiation of the PVA film containing the most suitable MV²⁺ concentration, can be satisfactorily related to the absorbed dose over a wide range, from 50 Gy up to 40 kGy. The effects of dose, dose rate, humidity and temperature on the response of the PVA-MV²⁺ dosimeter film have been studied under laboratory conditions. We conclude that the PVA film containing MV²⁺ is a promising tool for the absorbed dose measurements in several industrial applications of ionizing radiations.     

A study of radiation-chemical conversion of synthetic oil derived from oil-bitumen rock

The results of research in the radiation processing of synthetic oil derived from oil-bitumen rock of the Balakhany deposit in Azerbaijan are presented. The study has been conducted on a ⁶⁰Co gamma-source at a dose rate of P = 0.5 Gy/s and various absorbed doses of D = 43–216 kGy. Samples of synthetic oil from natural bitumen rocks have been analyzed by chromatography, gas chromatography-mass spectrometry, and IR spectroscopy, and their radiation resistance has been evaluated. The results of the study allow for both assessment of the feasibility of manufacturing petrochemicals for various applications by radiation processing and use of these materials for isolating radioactive sources to preclude their impact on the environment.     

Muscle and plastic equivalent glass dosimeter for high-dose dosimetry

The alkali-silicate glass dosimeter is made up of 66.8% SiO₂, 31.2% Li₂O, 2% K₂O. It is nearly colourless before irradiation and then takes on an amber colour with increasing doses of gamma-radiation. This colouration is represented by the appearance of broad absorption bands at 405 nm and 600 nm wavelengths. The change in absorbance is linear with the absorbed dose in the range 0.1–4.5 kGy, when measured at its 405 nm absorption band maximum. This glass dosimeter simulates low-z plastics and muscle tissue in terms of gamma-ray absorption properties over broad radiation spectra (0.1 MeV to 10 MeV).     

Dosimetric applications of α-alanine

Irradiation of solid polycrystalline alanine creates a free radical, whose concentration can be measured from its ESR signal. The radical CH₃HCOO^– of practically unlimited stability at room temperature shows an electronic absorption spectrum in the UV. Modern methods of diffuse reflectance spectrophotometry allow to measure the radical concentration which is proportional to the absorbed dose of radiation. The alanine dosimeter is prepared in a thin layer, adequate both for the congested isodose curves in the case of accelerated electrons irradiation and the method of measurement. Thus the proposed dosimeter is applicable not only for gamma, but also for EB radiation processing in the range of 0.1 to 50 kGy. The application of the dosimeter does not demand to use the ESR spectrometer, even of the type dedicated to alanine dosimetry only, but may be performed by a UV-VIS spectrophotometer equipped with an integrating sphere, permitting measurements of the Kubelka-Munk function.     

A new label dosimetry system based on pentacosa-diynoic acid monomer for low dose applications

The dosimetric characteristics of γ-radiation sensitive labels based on polyvinyl butyral (PVB) and a conjugated diacetylene monomer, 10,12-pentacosa-diynoic acid (PCDA) have been investigated using reflectance colorimeter. Two types of labels (colourless and yellow) based on PCDA monomer were prepared using an Automatic Film Applicator System. Upon γ-ray exposure, the colourless label turns progressively blue, while the yellow colour label turns to green then to dark blue. The colour intensity of the labels is proportional to the radiation absorbed dose. The useful dose range was 15 Gy-2 kGy depending on PCDA monomer concentration. The expanded uncertainty of dose measurement of the colourless label was 6.06 (2σ).     

Enhancement in sensitivity of nitro blue tetrazolium polyvinyl alcohol film dosimeters by sodium formate and Triton X-100

Nitro blue tetrazolium polyvinyl alcohol film dosimeters, NBT-PVA were prepared and evaluated based on radiation-induced reduction of NBT²⁺. NBT-PVA film dosimeters containing different concentrations of NBT dye from 1 to 5 mM were prepared in a solution of ethanol. The dosimeters were irradiated with ?-ray from ⁶⁰Co source at doses up to 50 kGy. UV/vis spectrophotometer was used to investigate the optical density of un-irradiated and irradiated films in terms of absorbance at 529 nm. The absorbance increases with absorbed dose up to 50 kGy for NBT-PVA film dosimeters. The dose sensitivity of NBT-PVA film increases strongly with increase of concentrations of NBT dye. The effects of irradiation temperature, humidity, dose rate and the stability of the response of the films after irradiation were investigated. A considerable increase was observed in the dose response of NBT-PVA film by adding appropriate concentration of sodium formate and Triton X-100.     

Combustion synthesis and luminescent properties of metal yttrium borates M3Y2 (BO3)4:Eu3+ (M = Ba,Sr) for PDPs applications

The polycrystalline powder samples of Eu³⁺ activated; mixed metal yttrium borate phosphors M₃Y₂(BO₃)₄ (M = Ba, Sr) with improved color purity of red emission for plasma display panels (PDPs) were prepared by solution combustion technique. The synthesis is based up on the exothermic reaction between the fuel (Urea) and oxidizer (Ammonium nitrate) .The heat generated in the reaction is utilized for auto combustion of ingredients. The formation of desired product and crystal structure was confirmed by powder XRD technique; while particle morphology was studied using FE-SEM. Samples under 254 and 147 nm excitation showed intense and pure red emission around 613 nm corresponding to the electric dipole ⁵D₀ → ⁷F₂ transition of Eu³⁺, CIE chromaticity coordinates of synthesized phosphors was found to be (x = 0.67, y = 0.32) close to National Television Standard Committee (NTSC) for red color; found suitable to employ in plasma display panels (PDPs) applications.