Dose response and post-irradiation characteristics of the Sunna 535-nm photo-fluorescent film dosimeter

Results of characterization studies on one of the first versions of the Sunna photo-fluorescent dosimeter™ have previously been reported, and the performance of the red fluorescence component described. This present paper describes dose response and post-irradiation characteristics of the green fluorescence component from the same dosimeter film (Sunna Model γ), which is manufactured using the injection molding technique. This production method may supply batch sizes on the order of 1 million dosimeter film elements while maintaining a signal precision (1σ) on the order of ±1% without the need to correct for variability of film thickness. The dosimeter is a 1 cm×3 cm polymeric film of 0.5-mm thickness that emits green fluorescence at intensities increasing almost linearly with dose. The data presented include dose response, post-irradiation growth, heat treatment, dosimeter aging, dose rate dependence, energy dependence, dose fractionation, variation of response within a batch, and the stability of the fluorimeter response. The results indicate that, as a routine dosimeter, the green signal provides a broad range of response at food irradiation (0.3–5 kGy), medical sterilization (5–40 kGy), and polymer cross-linking (40–250 kGy) dose levels.     

The effect of humidity on dehydration behavior of nitrofurantoin monohydrate studied by humidity controlled simultaneous instrument for X-ray Diffractometry and Differential Scanning Calorimetry (XRD–DSC)

The dependence of thermal dehydration behavior of nitrofurantoin monohydrate on humidity was studied. Difference in observed crystallinity of resulting anhydrates under three humidity conditions is discussed in relation to the effect of water vapor molecules. Thermal dehydration of nitrofurantoin monohydrate was measured using a humidity controlled simultaneous measurement instrument for X-ray Diffractometry (XRD) and Differential Scanning Calorimetry (DSC) in dry, 27 °C 91% RH and 60 °C 90% RH nitrogen. Dehydration of nitrofurantoin in dry nitrogen gave a mixture of crystalline and amorphous anhydrates in the temperature range of 124–180 °C followed by crystallization around 185–190 °C. Whereas, dehydration in high humidity atmosphere (60 °C 90% RH or 17.7% H₂O–82.3% N₂) gave well crystallized anhydrate at 140 °C soon after dehydration. Dehydration in low humidity nitrogen (27 °C 91% RH or 3.2% H₂O–96.8% N₂) gave not totally crystalline anhydrate, which became pure crystalline at around 190 °C. The effect of high humidity on dehydration and crystallinity of the resulting anhydrate can be attributed to the role of water vapor molecules in two ways such as the acceleration of molecular mobility and high molecular diffusion rate of nitrofurantoin anhydrate, and the formation of hydrogen bonding bridges quickly connecting dehydrated molecules to one another.     

Thermoluminescence characteristics of minerals from irradiated potatoes of different origins of production

Thermoluminescence (TL) characteristics were investigated for minerals, which were separated from potatoes irradiated at 0–1 kGy of different origins of production in Korea. The polyminerals analyzed by X-ray diffractometer were mainly composed of quartz and feldspar, and showed varied contents with producing origins, that contributed to typical TL responses to irradiation. The glow curve of irradiated samples at 0.05–1 kGy peaked at approximately 200°C with high intensity, but that of non-irradiated potatoes was observed at approximately 300°C with low intensity. Discrimination between irradiated (more than 0.05 kGy) and non-irradiated samples was possible just on the basis of the first glow curve, however, normalization of results through a re-irradiation step greatly improved their reliability. The signal intensity of TL decreased with the lapse of post-irradiation time under different storage conditions (0±0.5°C/dark room, 25±5°C/dark room and 25±5°C/naturally lighted room) but was still distinguishable from that of the non-irradiated sample even after one year.     

Sunna dosimeter: an integrating photoluminescent film and reader system; work in progress

A new radiation dosimeter, consisting of an optically-stimulated polymer film containing a photofluorescent sensor, can serve as a routine dosimeter and radiographic imaging medium for high-dose applications in the absorbed dose range 0.1–100 kGy. The flexible, colorless, opalescent film having a uniform thickness of 0.240 (±0.005) mm or certain other films in the thickness range 0.08–0.60 mm, are available in large batches. They can be read rapidly with a simple table-top spectrofluorimeter, excitation wavelength (λ=450 nm) and emission wavelength (λ=670 nm), giving a type A uncertainty of dose evaluation of <±5% at 95% confidence level. It supplies either single integrated dose readings or two-dimensional radiographic images with relatively high spatial resolution. The present work focuses on the following gamma-ray response characteristics of the system: inter- and intra-batch reproducibility, pre- and post-irradiation stability, and dependence of dose interpretations on absorbed dose rate and irradiation temperature.     

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.     

Reduction of Escherichia coli 0157:H7 in shredded iceberg lettuce by chlorination and gamma irradiation

Lettuce was inoculated with a six-strain cocktail of acid-adapted Escherichia coli 0157:H7 at a level of 1×10⁷ CFU/g. Following chlorination at 200 μg/ml, the lettuce was irradiated at 0.15, 0.38, or 0.55 kGy using a ⁶⁰Co source. Survival of E. coli 0157:H7, aerobic mesophiles and yeast and molds were measured over a period of 10 days. For quality analysis, chlorinated lettuce was subjected to irradiation at 0.33 and 0.53 kGy and stored at 1.0°C, 4.0°C or 7.0°C. Changes in texture and color were determined by instrumental means and changes in flavor, odor, and visual quality were determined by sensory testing.

Chlorination plus irradiation at 0.55 kGy produced a 5.4−log reduction in E. coli 0157:H7 levels. Chlorination alone reduced the E. coli 0157:H7 counts by 1–2 logs. Irradiation at 0.55 kGy was also effective in reducing standard plate counts and yeast and mold counts. Irradiation at this level did not cause softening of lettuce and sensory attributes were not adversely affected. In general, appearance and flavor were affected more by the length of storage than by temperature conditions. The 5+log reduction in E. coli counts and lack of adverse effects on sensory attributes indicate that low-dose irradiation can improve the safety and shelf-life of fresh-cut iceberg lettuce for retail sale or food service.     

The system CePO4–K3PO4

The phase diagram of the system CePO₄–K₃PO₄ has been determined based on investigations by differential thermal analysis, X-ray powder diffraction, IR spectroscopy and optical microscopy. The system contains only one intermediate compound K₃Ce(PO₄)₂, which melts incongruently at (1500±20)°C. This compound is stable down to room temperature and exhibits a polymorphic transition at 1180°C. It was confirmed that the low-temperature form β-K₃Ce(PO₄)₂ crystallizes in a monoclinic system, space group P2₁/m with unit cell parameters a=9.579 (5), b=5.634 (6), c=7.468 (5) Å; =γ=90°, β=90.81 (3)°; V=403.083 Å³.     

Syntheses, crystal structures and electronic properties of a series of copper(II) complexes with 3,5-halogen-substituted Schiff base ligands and their solutions

We have systematically investigated the structural features, electronic properties, thermally-induced structural phase transitions and absorption spectra depending on the solvent for ten Cu(II) complexes with 3,5-halogen-substituted Schiff base ligands. Structural characterization of two new complexes, bis(N-R-1-phenylethyl- and N-R,S-2-butyl-5-bromosalicydenaminato-κ²N,O)copper(II), reveals that they afford a compressed tetrahedral trans-[CuN₂O₂] coordination geometry with trans-N–Cu–N = 159.4(2)° and trans-O–Cu–O = 151.7(3)° for the 1-phenylethyl complex and trans-N–Cu–N = 157.9(3)° and trans-O–Cu–O = 151.0(3)° for the 2-butyl one. All the complexes exhibit a structural phase transition by heating in the solid state regardless of their structures at room temperature. The absorption spectra of a series of ten complexes exhibit a slight shift of the d–d band at 16 000–20 000 cm⁻¹ and remarkable shift of the π–π* band at 24 000–28 000 cm⁻¹, which suggests that the dipole moment of the solvents presumably affects the conformation of the π-conjugated moieties of the ligands rather than the coordination environment. We have also attempted ‘photochromic solute-induced solvatochromism’ by a system of bis(N-R-1-phenylethyl-3,5-dichlorosalicydenaminato-κ²N,O)copper(II) and photochromic 4-hydroxyazobenzene in chloroform solution. We successfully observed a change of the d–d and π–π* bands of the complex in the absorption spectra caused by cis–trans photoisomerization of 4-hydroxyazobenzene.     

Raman scattering study of highly fluorinated graphite

Raman spectra of highly fluorinated C_xF samples (1<x<2) prepared at room temperature and 515°C were measured. C_xF samples prepared at room temperature exhibited two Raman bands at 1593–1583 and 1555–1542 cm⁻¹. Graphite samples fluorinated at 515°C for 1 and 2 min also gave similar bands at 1581–1580 and 1550–1538 cm⁻¹. However, graphite samples fluorinated from 15 min to 10 h at 515°C no longer showed such spectra. The Raman peaks shifted to lower frequencies with increasing fluorine concentration in C_xF. This trend is due to the weakening of the C---C bonds of the graphene layers. Observation of both kinds of Raman bands suggests the coexistence of two highly fluorinated phases, C₂F and C₁F, in the samples. The process of formation of graphite fluoride is discussed on the basis of the Raman spectra of C_xF samples obtained at 515°C.     

Effect of gamma radiation on growth and survival of common seed-borne fungi in India

The present work describes radiation-induced effects of major seeds like Oryza sativa Cv-2233, Oryza sativa Cv-Shankar, Cicer arietinum Cv-local and seed-borne fungi like Alternaria sp., Aspergillus sp., Trichoderma sp. and Curvularia sp. ⁶⁰Co gamma source at 25 °C emitting gamma ray at 1173 and 1332 keV energy was used for irradiation. Dose of gamma irradiation up to 3 kGy (0.12 kGy/h) was applied for exposing the seed and fungal spores. Significant depletion of the fungal population was noted with irradiation at 1–2 kGy, whereas germinating potential of the treated grain did not alter significantly. However, significant differential radiation response in delayed seed germination, colony formation of the fungal spores and their depletion of growth were noticed in a dose-dependent manner. The depletion of the fungal viability (germination) was noted within the irradiation dose range of 1–2 kGy for Alternaria sp. and Aspergillus sp., while 0.5–1 kGy for Trichoderma sp. and Curvularia sp. However, complete inhibition of all the selected fungi was observed above 2.5 kGy.     

Infrared and Raman spectra, conformational stability, ab initio calculations of structure, and vibrational assignment of 2-hexyne

The infrared spectra (3500–50 cm⁻¹) of the gas and solid and the Raman spectra (3500–50 cm⁻¹) of the liquid and solid have been recorded for 2-hexyne, CH₃–CC–CH₂CH₂CH₃. Variable temperature studies of the infrared spectrum (3500–400 cm⁻¹) of 2-hexyne dissolved in liquid krypton have also been recorded. Utilizing four anti/gauche conformer pairs, the anti(trans) conformer is found to be the lower energy form with an enthalpy difference of 74±8 cm⁻¹ (0.88±0.10 kJ/mol) determined from krypton solutions over the temperature range −105 to −150 °C. At room temperature it is estimated that there is 42% of the anti conformer present. Equilibrium geometries and energies of the two conformers have been determined by ab initio (HF and MP2) and hybrid DFT (B3LYP) methods using a number of basis sets. Only the HF and DFT methods predict the anti conformer as the more stable form as found experimentally. A vibrational assignment is proposed based on the force constants, relative intensities, depolarization ratios from the ab initio and DFT calculations and on rotational band contours obtained using the calculated equilibrium geometries. From calculated energies it is shown that the CH₃ group exhibits almost completely free rotation which is in agreement with the observation of sub-band structure for the degenerate methyl vibrations from which values of the Coriolis coupling constants, ζ, have been determined. The results are compared to similar properties of some corresponding molecules.     

Practical results of Co production at RBMK-reactors

The paper presents practical results of ⁶⁰Co production in irradiation assemblies (IAs) in RBMK-1000 reactor during 1100 effective days of irradiation. Operational support of irradiation was performed by means of certified software system SAPFIR&RC-RBMK_RT. Integrity of IA in operating reactor was monitored by design system: no leaks in IAs were detected. Activity of ⁶⁰Co contained in each capsule was measured in the hot cell by comparison, using reference dosimeter with absorbed gamma-dose rate measurement uncertainty not more than ±3% at confidence probability P=0.95. Total amount of ⁶⁰Co produced was 2 MCi, average specific activity of ⁶⁰Co—52±7 Ci/g. Achievable specific activity of ⁶⁰Co in RBMK-reactor is 90±7 Ci/g and annual production capacity—about 8 MCi.     

Photo-luminescence of Risø B3 and PVB films for application in radiation dosimetry

Risø B3 film dosimeters (23 μm) prepared from poly(vinyl butyral) (PVB) incorporating pararosaniline cyanide, as the radiation-sensitive element and PVB films (25 μm) prepared from PVB without any additives are investigated for γ-radiation measurement using spectrofluorimetry based on their emission properties. The unirradiated Risø B3 film when excited at 554 nm shows an emission band at 602 nm while PVB film shows an emission band at 305 nm when excited at 235 nm wavelength. The fluorescence intensity of both emission bands decreases with the increase of absorbed dose due to the damage caused by ionizing radiation. The useful dose range of Risø B3 film extends up to 120 kGy while that of PVB film extends up to 60 kGy. The response of Risø B3 film increases with the increase of relative humidity during irradiation while that of PVB has less effect in the humidity range of 20–70%. The percent uncertainty associated with the measurement of the dose response was found to be ±3% (1σ) for both films. Risø B3 and PVB films show good post-irradiation stability in dark and indirect daylight where the deviation in the response overall a 2-month storage period was found to be ±5% for Risø B3 and ±2% for PVB.     

Freezing of water bound in lichen thallus as observed by H NMR. II. Freezing protection mechanisms in a cosmopolitan lichen Cladonia mitis and in Antarctic lichen species at different hydration levels

Proton NMR spectra at 300 MHz for dehydrated and hydrated thallus of Cladonia mitis Sandst. [=C. arbuscula (Wallr.) Flot ssp. Mitis (Sandst.) Ruoss], Himantormia lugubris (Hue) Lamb and Usnea aurantiaco-atra (Jacq.) Bory were recorded. The temperature was decreased from room temperature down to −45 °C. Pulse length was set to π/2=8.3 μs, which allowed the observation of tightly bound and loosely bound/or free water fraction, whereas the signal from solid matrix of thallus was reduced. In hydrated thallus a narrow Lorentzian line coming from loosely bound/free water fraction was recorded. For the temperature range between −5 and −20 °C a discontinuous increase in line halfwidths, accompanied by a decrease in area under the peak, was observed. This was attributed to the cooperative freezing of bulk water present in lichen thallus. In dehydrated thallus the NMR line consists of two components: a narrow, Lorentzian one (coming from loosely bound/free water fraction) and a broad line (from water tightly bound in lichen thallus). The overall area under peak remains unchanged down to −5 °C, and then between −5 and −20 °C it continuously decreases due to non-cooperative water immobilisation. As the temperature is decreased, for temperatures above −5 °C, the contribution made by the broad line component increases at the expense of the narrow line component. The mechanism of loosely-to-tightly bound water transfer is, at least partially, responsible for the freeze-protection of thallus in the lichen species investigated. No significant differences between the freeze protecting loosely-to-tightly bound water transfer mechanism of Antarctic lichens and that of cosmopolitan lichens was noticed.     

Ribosome kinetics and aa-tRNA competition determine rate and fidelity of peptide synthesis

It is generally accepted that the translation rate depends on the availability of cognate aa-tRNAs. In this study it is shown that the key factor that determines translation rate is the competition between near-cognate and cognate aa-tRNAs. The transport mechanism in the cytoplasm is diffusion, thus the competition between cognate, near-cognate and non-cognate aa-tRNAs to bind to the ribosome is a stochastic process. Two competition measures are introduced; C(i) and R(i) (i = 1, 64) are quotients of the arrival frequencies of near-cognates vs. cognates and non-cognates vs. cognates, respectively. Furthermore, the reaction rates of bound cognates differ from those of bound near-cognates. If a near-cognate aa-tRNA binds to the A site of the ribosome, it may be rejected at the anti-codon recognition step or proofreading step or it may be accepted. Regardless of its fate, the near-cognates and non-cognates have caused delays of varying duration to the observed rate of translation. Rate constants have been measured at a temperature of 20 °C by (Gromadski, K.B., Rodnina, M.V., 2004. Kinetic determinants of high-fidelity tRNA discrimination on the ribosome. Mol. Cell 13, 191–200). These rate constants have been re-evaluated at 37 °C, using experimental data at 24.5 °C and 37 °C (Varenne, S., et al., 1984. Translation in a non-uniform process: effect of tRNA availability on the rate of elongation of nascent polypeptide chains. J. Mol. Biol. 180, 549–576). The key results of the study are: (i) the average time (at 37 °C) to add an amino acid, as defined by the ith codon, to the nascent peptide chain is: τ(i) = 9.06 + 1.445 × [10.48C(i) + 0.5R(i)] (in ms); (ii) the misreading frequency is directly proportional to the near-cognate competition, E(i) = 0.0009C(i); (iii) the competition from near-cognates, and not the availability of cognate aa-tRNAs, is the most important factor that determines the translation rate – the four codons with highest near-cognate competition (in the case of E. coli) are [GCC] > [CGG] > [AGG] > [GGA], which overlap only partially with the rarest codons: [AGG] < [CCA] < [GCC] < [CAC]; (iv) based on the kinetic rates at 37 °C, the average time to insert a cognate amino acid is 9.06 ms and the average delay to process a near-cognate aa-tRNA is 10.45 ms and (vii) the model also provides estimates of the vacancy times of the A site of the ribosome – an important factor in frameshifting.     

Characterisation of absorptive sampling with SPME fibres in the EUPHORE photoreactor

The implementation of an experimental set-up for sampling, and characterisation of parameters related to absorptive sampling solid phase microextraction (SPME) in the EUPHORE photoreactor is described. Toluene was taken as probe compound. Optimisation of the sampling and calibration curves are presented. Equilibrium was achieved in just 30 s due to the good agitation in the chambers and the LOD was 0.24 ppbV. The precision was ±0.02 expressed as relative standard deviation (n = 9). The inter-fibre reproducibility was ±0.03 expressed as relative standard deviation. The effect of the temperature and the sun radiation on absorption in the fibre is also studied using a relative method to calculate the ratio K/K₀ (ratio of absorption constants at two different times during the experiment at which temperature and radiation conditions experimented important variations) calculated through known parameters, avoiding in this way the need for external calibrations in the calculation of K. The results showed a difficult to predict dependence of absorption over the combination of temperature and sun radiation and the need to develop sampling systems with absorptive SPME in which sun radiation has no influence. The stability in different conditions of compounds absorbed in the fibre was also subject to study. At room temperature half of the compound absorbed is expected to desorb in 1.21 h. Conversely, when fibres were kept at low temperatures (−86 °C) after 21 days, desorption was negligible.     

On the thermodynamic equilibrium between ice and electrolyte solutions in the conditions of confined geometry

For a small volume (of about 10⁻⁶ cm³) of NaCl and other electrolyte solutions (C = 0.1 and 1 M) in thin (r = 5/10 μm) single quartz capillaries, dependencies of the column length l of frozen solutions on the temperature t were measured using comparator IZA-2 in a thermostated chamber. At temperatures range t > −4 °C (for C = 0.1 M) and t > −8 °C (for C = 1 M) the l(t) dependencies are reversible and therefore correspond to establishment of an equilibrium between ice-1 and the solution.

From the constants mass condition of the dissolved salt in a frozen column, the l(t) expression was derived, which includes thermodynamic relation between solution concentration in an equilibrium with ice, C_s, and the temperature t for bulk systems. Deviations from the data known for bulk solutions were observed in thin capillaries when temperature t decreased to −3 °C (for 0.1 M NaCl) and to −6 °C for 1 M NaCl solution.

This effect may be a result of strong adhesion of the ice column to capillary walls. In this case, some internal stresses arise in frozen solution resulting in a deviation from thermodynamic equilibrium conditions for bulk systems. When approaching the temperature of ice melting, adhesion forces decrease due to formation of a thin non-freezing water interlayer on the capillary wall. In this temperature range the experimental data are in agreement with the predictions for bulk systems. It was supposed that the observed deviation in thin capillaries may be caused by formation of an amorphous ice phase with higher density as compared with the ice-1 during rapid freezing, or by an effect of ice microlenses formation. Both effects will result in a deviation from the phase diagram corresponding to a bulk solution.     

Effects of temperature and humidity during irradiation on the response of radiachromic film dosimeters

The effects of temperature and humidity during γ irradiation on the response of two types of film dosimeters (Far Wesr radiachromic and GafChromic films) were studied in the dose range of 0.3–3 kGy. Both films show a significant effect of temperature and humidity and a simple correction function is proposed. This correction is usually between 5 and 10% for the range studied.

For the GafChromic film, a colour change at temperatures above 50°C was observed and, consequently, this system cannot be used at these temperatures. At lower temperatures down to - 70°C the sensitivity of both films is reduced and a simple correction is possible. In this study and for the dose ranges used, only a slight dependence on humidity was observed for both films from 0 to 60% r.h. Whereas the GafChromic film at humidities up to 90% r.h. shows only a moderate effect, the Far West films shows a considerable inconsistency for the dose range studied. A simple correction function may be applied for humidity effects, except for the Far West film above 60% r.h. where the effect of humidity is also dose dependent.     

Thermal- and photo-induced transformations of N-aryl-N-nitrosohydroxylamine ammonium salts to azoxy compounds

Heating of an ethanolic solution containing N-aryl-N-nitrosohydroxylamine ammonium salts at 78 °C produced the desired azoxy compounds in 80–93% yields. Furthermore, irradiation with UV light (λ≥300 nm) of ethanolic solutions of those ammonium salts at room temperature also provided the desired azoxy compounds in 51–72% yields.     

Phase transformation on heating of an aged cement paste

The standard cement paste (C-43-St) was studied previously by static heating, SH, immediately after 1 month hydration at w/c = 0.4 [J. Therm. Anal. Calorim. 69 (2002) 187]. This paste after 5-year ageing (unprotected from contact with air) was subject to thermal analysis in air and in argon (DTA, DTG and TG), to XRD at various temperatures, T, in a high temperature chamber, to mass spectroscopy (MS) and to IR spectroscopy. The aim of this study was to compare the results of SH (fresh paste) and of TG (the aged one), to verify the assumptions made on SH interpretation and to check the change in hydration products with ageing as measured by phase transformation on heating (ΔM versus the final mass). The sorbed water (EV), escaping at 110 °C from the fresh paste, was bound on ageing with a higher energy and escaped at higher temperatures. The joint water content of hydrates and of C-S-H gel increased on ageing by 1–2% in the dense paste C-43-St and did not change in the less compact one C-43-I. C-S-H gel transformed on heating above 600 °C into C₂S and C₃S. Portlandite content did not change on ageing. In the air atmosphere it became partly carbonated, which was accompanied by an increase in mass between 500 and 600 °C. Carbon dioxide and/or carbonate ions to form carbonates, were sorbed during ageing and were present in the aged paste in some form undetectable by XRD (amorphous or crypto-crystalline). Sensitivity to carbonation ΔM(700–800 °C) increased highly with ageing.