Gamma-photon induced modifications in Polyvinylchloride (PVC) film

Gamma photon induced modifications in Polyvinylchloride (PVC) polymer have been studied in the dose range of 10¹-10⁶Gy at room temperature. Polyvinylchloride films have been irradiated with different doses of gamma radiation from a ⁶⁰Co source. To monitor the chemical and structural changes caused by gamma radiation IR and UV-Vis spectroscopy of pristine and irradiated PVC have been performed and using the spectral data some changes in the properties have been investigated. The spectral studies have indicated that at a dose of 10⁶Gy scissioning of the C-a bonds takes place. This scissioning of the chain initiates decomposition at a lower temperature. Thermal stability of the polymer reduces due to irradiation but the decomposition patterns remain the same. The optical band-gap is found to decrease due to irradiation at doses bigher than 10³Gy.     

Spectroscopic and thermal studies of gamma irradiated polypropylene polymer

Thin films of polypropylene have been irradiated with different doses of gamma radiation from a ⁶⁰Co source. IR, UV-VIS spectra of this polymer before and after irradiation have been recorded and from the spectral data some modifications in the properties have been investigated. The spectra indicated that polypropylene film was oxidised at the dose of 10⁶ Gy. Due to the removal of additives, total destruction of the polymer takes place at this dose. Isotactic arrangement of the polymer is no longer present after irradiation. Growth of carbon cluster takes place above a gamma dose of 10² Gy. Thermal stability of the polymer changes due to irradiation and the polymer seems to decompose in four different steps at the highest dose of 10⁶ Gy.     

Effect of gamma irradiation on the structural,thermal and optical properties of Makrofol BL 2–4

Makrofol BL 2–4 is an extrusion film based on Makrolon polycarbonate. It comprises excellent die-cutting performance combined with high light transmission and moderate light scattering properties. It is a class of polymeric solid state nuclear track detectors which has many applications in various radiation detection fields. In the present work, Makrofol samples were irradiated using different gamma doses ranging from 10 to 350 kGy. The structural modifications in the gamma-irradiated Makrofol samples have been studied as a function of dose using different characterization techniques such as X-ray diffraction, intrinsic viscosity, Fourier transform infrared spectroscopy, thermogravimetric analysis, refractive index and color difference studies. The gamma irradiation in the dose range 20–200 kGy led to a more compact structure of Makrofol polymer, which resulted in an improvement in its thermal stability with an enhancement in its structural and optical properties.     

Changes produced in etching parameters of CR-39 by high-dose pre- and post-γ irradiation

The effect of post- and pre-high doses of γ–radiation in CR-39 plastic detectors has been studied in the dose range of 3×10¹?10⁶ Gy. Some properties like bulk-etch rate (V _B), track-etch rate (V _T), sensitivity (V _T/V _B) and efficiency have been found out for different gamma doses from a ⁶⁰Co source in CR-39. It is found that V _B and V _T remain almost invariant up to gamma doses of 10⁴ Gy. Then they start increasing slowly till 10⁵ Gy. Between 10⁵ Gy and 10⁶ Gy there is a sharp increase of V _B and V _T values for pre- and post-gamma exposed samples. The present data are compared with the previous literature.     

A comparative study of gamma radiation effects on track properties of different PADC detectors

Track properties of gamma-irradiated polyallyldiglycol carbonate (PADC) detectors (Homalite, Pershore and Trastrack) are studied in the dose range of 10¹–10⁶ Gy. Results show that the bulk and track etch rates of all three types of PADC detector increase at doses higher than 10⁴ Gy. This increase is more pronounced in post-gamma exposed detectors. The change in etch rate ratio (S) for post-gamma exposed PADC–Homalite detectors is more significant when compared with the other detectors. The critical angle for etching shows that etching at a low temperature of 60 °C is more effective, and the critical angle value is decreased to a significant extent for all three types of PADC detectors. Etching efficiency of post-gamma exposed samples is found to be much higher than the pre-gamma exposed sample at the highest dose of 10⁶ Gy. When compared, it was found that of the three PADC detectors, PADC–Homalite detectors seem to be more sensitive to gamma irradiation.     

Modification induced by gamma irradiation in Bayfol CR 1-4 polycarbonate

Bayfol CR 1-4 polycarbonate is a class of polymeric solid state nuclear track detector which has many applications in various radiation detection fields. Samples from sheets of Bayfol have been irradiated with gamma doses ranging from 100 to 620 kGy. The structural modifications in the gamma-irradiated Bayfol samples have been studied as a function of dose, using different characterization techniques such as X-ray diffraction (XRD), Fourier-transform infrared (FTIR) spectroscopy, intrinsic viscosity and refractive index. The results indicate that the carbonyl group (C?O) degraded under irradiation up to 200 kGy. This degradation, reported by FTIR spectroscopy enhanced the degree of ordering in the degraded samples as revealed by the XRD technique. Above 200 and up to 620 kGy, cross-linking is achieved, leading to an increase in the intrinsic viscosity from 0.41 to 0.78 at 35°C, indicating an increase in the average molecular mass. On the other hand, the resultant effect of gamma irradiation on the thermal properties of Bayfol has been investigated using thermo-gravimetric analysis, results indicating that the gamma irradiation in the dose range 200–620 kGy led to a more compact structure of Bayfol polymer, which resulted in an improvement in its thermal stability with an increase in the activation energy of thermal decomposition due to cross-linking. In addition, the V–I characteristics of the polymer samples were performed, results indicated that at higher voltage, the conduction mechanism of Bayfol CR 1-4 was identified as the Poole–Frenkel type.     

A study of the effect of gamma and laser irradiation on the thermal,optical and structural properties of CR-39 nuclear track detector

A comparative study of the effect of gamma and laser irradiation on the thermal, optical and structural properties of the CR-39 diglycol carbonate solid state nuclear track detector has been carried out. Samples from CR-39 polymer were classified into two main groups: the first group was irradiated by gamma rays with doses at levels between 20 and 300 kGy, whereas the second group was exposed to infrared laser radiation with energy fluences at levels between 0.71 and 8.53 J/cm². Non-isothermal studies were carried out using thermogravimetry, differential thermogravimetry and differential thermal analysis to obtain activation energy of decomposition and transition temperatures for the non-irradiated and all irradiated CR-39 samples. In addition, optical and structural property studies were performed on non-irradiated and irradiated CR-39 samples using refractive index and X-ray diffraction measurements. Variation in the onset temperature of decomposition T _o, activation energy of decomposition E _a, melting temperature T _m, refractive index n and the mass fraction of the amorphous phase after gamma and laser irradiation were studied.

It was found that many changes in the thermal, optical and structural properties of the CR-39 polymer could be produced by gamma irradiation via degradation and cross-linking mechanisms. Also, the gamma dose has an advantage of increasing the correlation between thermal stability of the CR-39 polymer and bond formation created by the ionizing effect of gamma radiation. On the other hand, higher laser-energy fluences in the range 4.27–8.53 J/cm² decrease the melting temperature of the CR-39 polymer and this is most suitable for applications requiring molding of the polymer at lower temperatures.     

Some thermo-stimulated luminescence parameters of quartz arenite relevant to gamma dosimetry

The thermo-stimulated luminescence (TSL) green emission band of natural quartz arenite was studied. The natural glow curve displayed a broad peak with the maximum at ～288 °C. The gamma (γ)-induced glow curves showed TSL peaks at 70 °C, 90 °C, 135 °C, 220 °C and 320 °C over the dose range of 1–10⁴ Gy. The trap parameters were calculated using the initial rise procedure. The γ-dose vs. TSL response was linear (uncertainty was within±3%) in the dose range of 1–100 Gy, above which sublinearity sets in. For the investigated material, the batch homogeneity has been calculated to be 0.28. Fading studies over a period of 5 days show that the γ-irradiated aliquots have a stable signal of 84%. The results are of importance in TSL dating, nuclear accident dosimetry, industry and for high-dose measurements.     

Effect of cobalt-60 gamma irradiation on graphene: Raman and field emission investigations

Electrophoretically deposited graphene (HG) on silicon is irradiated using a cobalt-60 gamma radiation source with the radiation dose up to 22.7 kGy. The effect of gamma irradiation on the field emission current noise behavior of HG is investigated. The power spectra of pristine and irradiated HG exhibit 1/f^α type of noise, with α ～ 0.8. The magnitude of noise power is observed to increase with the radiation dose. The variations in the turn on field and noise power in the emission current are attributed to the structural modifications of HG, as revealed from the field emission scanning electron microscopic and Raman spectroscopic studies.     

Thermoluminescence characterization of the Cu(Tb,Tm)-12CaO-7AL2O3 compounds obtained by combustion synthesis

The thermoluminescence (TL) properties of dode-calcium hepta-aluminate (Ca₁₂Al₁₄O₃₃) enabled by 12CaO-7Al₂O₃ doped with rare earth and transitions metals ions have been studied and their suitability for radiation dosimetry applications is discussed. It was observed that this calcium aluminate phase doped with Tm-Cu at concentration of 0.1 mol% is a good candidate for dosimetric applications since it presents well-defined single peak observed at 240 °C and 320 °C and a linear response to gamma radiation dose from 5 × 10⁻³ Gy up to 100 Gy.     

TL,OA and ESR of spessartine garnet

Thermoluminescence (TL), optical absorption (OA), electron spin resonance (ESR) and their relation to point defects in spessartine have been investigated. The TL glow curve presented four peaks at 150, 220, 260 and 335 °C. The 150 and 335 °C TL peaks growth curves presented a linear growth with radiation dose up to about 400 Gy, supralinearity above this dose, and saturation around 800–1000 Gy. The OA spectrum presented allowed spin transition bands due to Fe³⁺ and Mn²⁺ in dodecahedral environment. Absorption bands due to ultraviolet charge transfer of Fe³⁺ in octahedral and tetrahedral positions were also observed. Two ESR, a strong one around g?～?2 due to Fe³⁺ in octahedral position, and another weaker one at g?～?4 due to Fe³⁺ in tetrahedral position, have been detected. The effect of high temperature annealing (600–900 °C) before irradiation was also investigated.     

The real-time gamma radiation dosimetry with TeO2 thin films

A detailed study of the effect of gamma radiation on the current–voltage characteristics of the TeO₂ thin films of different thicknesses, prepared by thermal evaporation in a vacuum, has been carried out for a much wider range of the gamma radiation doses than made here-to-fore. Subsequently, for the thin films of different thicknesses at different applied voltages, the variations of the current density with dose have been obtained. The current density increases near linearly with the gamma radiation dose up to a critical radiation dose, a dose value higher for the thicker films and decreases thereafter. The sensitivities of these TeO₂ thin films at different applied voltages have been found to be in the range 1.2–37.0 nA/cm²/μGy. Correspondingly, the detection limits have also been estimated and have been found to be in the range 0.22–2.16 mGy. Clearly, the TeO₂ thin films have high potential for their use as real-time gamma radiation dosimeters in monitoring the gamma radiation doses under a variety of practical situations involving low level to high level of the doses.     

Gamma ray photon-induced modifications in Triafol-TN and Triafol-BN polymeric track detectors

Photon induced modifications in Triafol-TN and Triafol-BN polymers have been studied in the dose range of 10¹–10⁶ Gy at room temperature using a ⁶⁰Co source. To monitor the chemical and structural changes induced by gamma rays, UV, IR, and ESR studies were carried out. Thermal studies were also conducted for understanding the effects of gamma irradiations on these polymers. Variation of track etching characteristics and activation energy for bulk etching have been studied at different gamma rays doses. The experimental results are presented and discussed.     

Enhancement in electrochemical properties of ionic liquid-based nanocomposite polymer electrolytes by 100 MeV Si9+ swift heavy ion irradiation

Swift heavy ion (SHI) irradiation has been used as a tool to enhance the electrochemical properties of ionic liquid-based nanocomposite polymer electrolytes dispersed with dedoped polyaniline (PAni) nanorods; 100 MeV Si⁹⁺ ions with four different fluences of 5?×?10¹⁰, 1?×?10¹¹, 5?×?10¹¹, and 1?×?10¹² ions cm^?2 have been used as SHI. XRD results depict that with increasing ion fluence, crystallinity decreases due to chain scission up to fluence of 5?×?10¹¹ ions cm^?2, and at higher fluence, crystallinity increases due to cross-linking of polymer chains. Ionic conductivity, electrochemical stability, and dielectric properties are enhanced with increasing ion fluence attaining maximum value at the fluence of 5?×?10¹¹ ions cm^?2 and subsequently decrease. Optimum ionic conductivity of 1.5?×?10^?2 S cm^?1 and electrochemical stability up to 6.3 V have been obtained at the fluence of 5?×?10¹¹ ions cm^?2. Ac conductivity studies show that ion conduction takes place through hopping of ions from one coordination site to the other. On SHI irradiation, amorphicity of the polymer matrix increases resulting in increased segmental motion which facilitates ion hopping leading to an increase in ionic conductivity. Thermogravimetric analysis (TGA) measurements show that SHI-irradiated nanocomposite polymer electrolytes are thermally stable up to 240–260 °C.     

Induced Electronic and Thermal Effects of 86 MeV Nickel Ions in Bisphenol-A Polycarbonate

Bisphenol-A polycarbonate films were irradiated with 86 MeV swift heavy nickel ions at varying fluences, ranging from 1 × 10¹¹ to 1 × 10¹³ ions cm^?2, under vacuum at room temperature, to analyze the induced electrical and thermal modifications. AC conductivity measurements and UV-visible spectroscopy, Fourier transform infra-red (FTIR) spectroscopy, thermo-gravimetric analysis (TGA), differential scanning calorimetry (DSC), and X-ray diffraction (XRD) techniques were applied to analyze the changes. A significant, exponential increase in conductivity at higher frequency was observed with the increase of nickel ion fluence. UV-visible analysis corroborated the results of the AC conductivity measurement, revealing the increase in size of the carbon clusters embedded in the polymer network, with the increase of heavy ion fluence. FTIR analysis revealed the formation of alkene and alkyne end groups at higher doses, which further supported the suggestion that the variation in electrical properties induced by the ion irradiation of the polymer was due to development of a carbonaceous phase inside the polymer due to the irradiation. Thermal analysis, i.e., TGA and DSC patterns, showed that chain-scission was the leading phenomena in the heavy ion-irradiated polycarbonate samples, resulting in degradation of their thermal stability.     

Carbon (70 MeV) and copper (120 MeV) ions irradiation effects in Makrofol-N

Makrofol-N polycarbonate was irradiated with carbon (70 MeV) and copper (120 MeV) ions to analyze the induced effects with respect to optical and structural properties. In the present investigation, the fluence for carbon and copper beams was kept in the range of 1×10¹¹– 1×10¹³ ions/cm² to study the swift heavy ion induced modifications. UV–VIS, FTIR and XRD techniques were utilized to study the induced changes. The analysis of UV–VIS absorption studies revealed that the optical energy gap was reduced by 17% on carbon irradiation, whereas the copper beam leads to a decrease of 52% at the highest fluence of 1×10¹³ ions/cm². The band gap can be correlated to the number of carbon atoms, N, in a cluster with a modified Robertson's equation. In copper (120 MeV) ions irradiated polycarbonate, the number of carbon atoms in a cluster was increased from 63 to 269 with the increase of ion fluence from 0 to 1×10¹³ ions/cm², whereas N is raised only up to 91 when the same polymer films were irradiated with carbon (70 MeV) ions under similar conditions. FTIR analysis showed a decrease in almost all characteristic absorption bands under irradiation. The formation of hydroxyl (? OH) and alkene (C?C) groups were observed in Makrofol-N at higher fluence on irradiation with both types of ions, while the formation alkyne end (R? C≡ CH) group was observed only after copper ions irradiation. The radii of the alkyne production of about 3.3 nm were deduced for copper (120 MeV) ions. XRD measurements show a decrease in intensity of the main peak and an increase of the average intermolecular spacing with the increase of ion fluence, which may be attributed to the structural degradation of Makrofol-N on swift ion irradiation.     

In-phantom neutron dose distribution for bladder cancer cases treated with high-energy photons

This work presents an estimation of the neutron dose distribution for common bladder cancer cases treated with high-energy photons of 15 MV therapy accelerators. Neutron doses were measured in an Alderson phantom, using TLD 700 and 600 thermoluminescence dosimeters, resembling bladder cancer cases treated with high-energy photons from 15 MV LINAC and having a treatment plan using the four-field pelvic box technique. Thermal neutron dose distribution in the target area and the surrounding tissue was estimated. The sensitivity of all detectors for both gamma and neutrons was estimated and used for correction of the TL reading. TLD detectors were irradiated with a Co⁶⁰ gamma standard source and thermal neutrons at the irradiation facility of the National Institute for Standards (NIS). The TL to dose conversion factor was estimated in terms of both Co⁶⁰ neutron equivalent dose and thermal neutron dose. The dose distribution of photo-neutrons throughout each target was estimated and presented in three-dimensional charts and isodose curves. The distribution was found to be non-isotropic through the target. It varied from a minimum of 0.23 mSv/h to a maximum of 2.07 mSv/h at 6 cm off-axis. The mean neutron dose equivalent was found to be 0.63 mSv/h, which agrees with other published literature. The estimated average neutron equivalent to the bladder per administered therapeutic dose was found to be 0.39 mSv Gy^?1, which is also in good agreement with published literature. As a consequence of a complete therapeutic treatment of 50 Gy high-energy photons at 15 MV, the total thermal neutron equivalent dose to the abdomen was found to be about 0.012 Sv.     

X-ray irradiation-induced changes in Bayfol DPF 5023 polycarbonate

Samples from sheets of the polymeric material Bayfol DPF 5023 have been exposed to X-ray radiation in the dose range 100–2300 Gy. The modifications induced in Bayfol samples due to X-ray irradiation have been studied through different characterization techniques such as X-ray diffraction (XRD), Fourier transform infrared (FTIR) spectroscopy, intrinsic viscosity, refractive index and color difference studies. The infrared spectroscopy indicated that crosslinking is the dominant mechanism at the dose range of 200–2300 Gy. The crosslinking reported by FTIR spectroscopy destroyed the degree of ordering in the Bayfol samples, as revealed by the XRD technique. Also, this crosslinking led to an increase in the value of intrinsic viscosity from 0.54 for the non-irradiated sample to 0.63 for the sample irradiated with 2300 Gy at 30 °C, indicating an increase in the average molecular mass. This was associated with an increase in the refractive index. Additionally, the non-irradiated Bayfol samples showed significant color sensitivity toward X-ray irradiation. This sensitivity appeared in the change of the blue color component of the non-irradiated Bayfol film to yellow after exposure to X-ray doses up to 2300 Gy. This is accompanied by a net increase in the darkness of the samples.     

Effect of nano-size fumed silica on ionic conductivity of PVdF-HFP-based plasticized nano-composite polymer electrolytes

Nano-composite polymer electrolytes containing poly(vinylidene fluoride-co-hexafluoropropylene) (PVdF-HFP), ammonium tetrafluoroborate (NH₄BF₄), and nano-size fumed silica (SiO₂) have been prepared and characterized by complex impedance spectroscopy. Ionic conductivity of polymer has been found to increase with the addition of NH₄BF₄, and a maximum conductivity of 3.62 × 10^?6 S/cm has been obtained at 30 wt% NH₄BF₄. The formation of ion aggregates at high concentration of salt has been explained by Bjerrum’s law and mass action considerations. The conductivity of polymer electrolytes has been increased by three orders of magnitude (10^?6 to 10^?3 S/cm) with the addition of plasticizer, and a maximum conductivity of 1.10 × 10^?3 S/cm has been observed at 80 wt% DMA. An increase in conductivity with the addition of nano-size fumed silica is attributed due to the formation of space-charge layers. A maximum conductivity of 7.20 × 10^?3 S/cm has been observed for plasticized nano-composite polymer electrolytes at 3 wt% SiO₂. X-ray diffraction analysis of polymer electrolyte system was also carried out. A small change in conductivity of nano-composite polymer electrolytes observed over the 30–130 °C temperature range and for a period of 30 days is also desirable for their use in various applications.     

Polyamide woven fabrics with 2,3,5-triphenyltetrazolium chloride or nitro blue tetrazolium chloride as 2D ionizing radiation dosimeters

The development of flat woven fabric-based ionizing radiation 2D dosimeters is reported in this work. Polyamide fabric was surface modified with radiation-sensitive 2,3,5-triphenyltetrazolium chloride (TTC) or nitro blue tetrazolium chloride (NBT). These samples responded to gamma radiation of ⁶⁰Co through a colour change: red and blue for TTC and NBT, respectively. The tinge intensity was observed to depend on the absorbed dose, which allowed for the reflectance of light (R) measurements and calculation of the calibration parameters: dose range, quasi-linear range, threshold dose and sensitivity. Oxygen was shown to be an important factor determining the dose response of the samples. For this reason, a range of additional modifications to the TTC- and NBT-polyamide fabric was proposed which lead to a decrease in the threshold dose and increase in the sensitivity to irradiation of the samples. For instance, a dosimeter made of polyamide fabric modified with 10 g/dm³ TTC, 0.5 mol/dm³ tert-butyl alcohol, 7.5% gelatine hydrogel at pH 10 (vacuum packed) showed the lowest dose threshold (50 Gy), dose range up to 2.8 kGy and the highest sensitivity to irradiation (?0.0396%/Gy) among the compositions studied. In consequence, this dosimeter was examined in terms of response to inhomogeneous irradiation from a ¹⁹²Ir brachytherapy radiation source. The relative dose distribution profiles across the source's longitudinal axis were calculated. This showed potential of the textile dosimeters for 2D dose distribution measurements; however, further modifications towards improvement of the dosimeter's low dose response can be considered.