Changes induced in structure and optical properties of PM-355 nuclear track detector due to laser irradiation

PM-355 is a class of polymeric solid-state nuclear track detectors which has a lot of applications in several radiation detection fields. Samples from sheets of PM-355 have been exposed to infrared (IR) laser fluences ranging from 1 to 12.8?J/cm². The effect of IR laser radiation on the structural properties of PM-355 has been investigated using X-ray diffraction and Fourier transform infrared spectroscopy. The results indicate that the samples exhibit chain scission under the effect of laser irradiation up to 4.2?J/cm², thus producing free radicals that led to the formation of new bonds started and continued until 12.8?J/cm². This reduces the ordering structure, giving the PM-355 polymer more resilience. In addition, the laser irradiation at the fluence range 4.2–12.8?J/cm² led to a more compact structure of PM-355, which resulted in an improvement in its isotropic nature with an increase in Vickers hardness and refractive index. Further, the color changes due to laser irradiation were computed using the transmission data in the wavelength range of 370–780?nm. It is found that the color intensity, which is the color difference between the irradiated samples and the non-irradiated one, increases with increasing the laser fluence, largely depending on the proportions of the blue color component.     

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.     

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 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.     

High energy electron irradiation effects on polystyrene films

The effect of an 8 MeV electron-beam on the structural, optical and dielectric properties of polystyrene films has been investigated respectively by means of Fourier transform infrared (FTIR) spectroscopy, ultraviolet–visible (UV–VIS) spectroscopy and electrical impedance (LCR) analysis over a radiation dose in the range of 50–250 kGy using a Microtron accelerator. The FTIR spectral analysis shows no change in the overall structure of the irradiated polystyrene films, except a minor change in the intensity of a few peaks in the FTIR spectrum, indicating that polystyrene is resistant to electron-beam irradiation over the range of radiation doses investigated. The optical band gap analysis using the UV–VIS absorption spectra of the polystyrene shows a small decrease in the optical band gap (E _g) and the activation energy with an increase in electron doses. Further, the dielectric measurements over a frequency range of 100 Hz to 1 MHz for the electron-beam-irradiated polystyrene films show that both the dielectric constant and the dielectric loss increase with an increase in electron radiation dose, which may be ascribed to the formation of defect sites in the band gap of polystyrene as a consequence of molecular chain scission in the polymer films upon irradiation.     

Effect of fast neutron irradiation on the structural and optical properties of Makrofol DE 1-1 CC polycarbonate

Samples from sheets of the polymeric material Makrofol DE 1-1 CC have been exposed to neutrons of incident energy in the range of 0.8–19.2 MeV. The modifications induced in Makrofol samples due to neutron 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. Infrared spectroscopy indicated that cross-linking is the dominant mechanism in the energy range of 2.3–19.2 MeV. The cross-linking reported by FTIR spectroscopy destroyed the degree of ordering in the Makrofol samples, as revealed by the XRD technique. Also, this cross-linking led to an increase in the values of intrinsic viscosity from 0.41 to 0.68 at 28 °C, indicating an increase in the average molecular mass, associated with an increase in the refractive index. Additionally, the non-irradiated Makrofol samples showed significant color sensitivity toward neutron irradiation. The sensitivity toward neutron irradiation can be seen by the change in the blue color component of the non-irradiated Makrofol film to yellow after the samples are exposed to neutrons up to 19.2 MeV. This is accompanied by a net increase in the darkness of the samples.     

Gamma irradiation effects on structural and optical properties of amorphous and crystalline Nb<Subscript>2</Subscript>O<Subscript>5</Subscript> thin films

The structural and optical properties of RF sputtered Nb₂O₅ thin films are studied before and after gamma irradiation. The films are subjected to structural and surface morphological analyses by using X-ray (XRD) and field emission scanning electron microscope techniques. In the wavelength range of 300–2000 nm, the optical parameters for amorphous and crystalline Nb₂O₅ thin films are estimated at differently exposed γ-irradiation doses (0, 50, 100 and 200 kGy). The optical constants, such as optical energy band gap, absorption coefficient, refractive index and oscillators parameters of amorphous and crystalline Nb₂O₅ thin films are calculated. The optical band gaps of γ-irradiated amorphous and crystalline Nb₂O₅ thin films are determined. In the non-absorbing region, the real part of the refractive index of amorphous and crystalline Nb₂O₅ thin films slightly increases with the increase in the exposed γ-irradiation dose.     

Effect of electron beam irradiation on the structural,thermal and optical properties of poly(vinyl alcohol) thin film

Poly(vinyl alcohol) (PVA) polymer was prepared using the casting technique. The obtained PVA thin films have been irradiated with electron beam doses ranging from 20 to 300 kGy. The resultant effect of electron beam irradiation on the structural properties of PVA has been investigated using X-ray diffraction (XRD) and Fourier transform infrared spectroscopy (FTIR), while the thermal properties have been investigated using thermo-gravimetric analysis and differential thermal analysis (DTA). The onset temperature of decomposition T ₀ and activation energy of thermal decomposition E _a were calculated, results indicate that the PVA thin film decomposes in one main weight loss stage. Also, the electron beam irradiation in dose range 95–210 kGy led to a more compact structure of the PVA polymer, which resulted in an improvement in its thermal stability with an increase in the activation energy of thermal decomposition. The variation of transition temperatures with electron beam dose has been determined using DTA. The PVA thermograms were characterized by the appearance of an endothermic peak due to melting. In addition, the transmission of the PVA samples and any color changes were studied. The color intensity Δ E was greatly increased with increasing electron beam dose, and was accompanied by a significant increase in the blue color component.     

Electron beam induced modifications in crystalline structure of polyvinylidene fluoride/nanoclay composites

PVDF/nanoclay nanocomposites were prepared via melt mixing method. The intercalated dispersion of the nanoclay in PVDF matrix was confirmed by XRD. According to FTIR, DSC and XRD results, the presence of nanoclay facilitated transition from α-to-β crystalline phase. Electron beam irradiation decreased the melting point of the nanocomposites. The decrease in melting point of the nanocomposites was about 11 °C at 500 kGy. The crystallinity of nanocomposites increased at an irradiation dose of 100 kGy and decreased at higher irradiation doses. The extent of crosslinking of the nanocomposites increased significantly with irradiation up to 300 kGy. The nanoclay intensified the increase in yield strength with irradiation doses up to 300 kGy. The combination of nanoclay and irradiation had a synergistic effect on the increase of yield strength.     

Structural and optical modifications in gamma-irradiated polyimide/silica nanocomposite

The structural and optical properties of thin films of polyimide composites with nanosilica particle content of 15?wt%, prepared via sol–gel process, were studied as a function of the gamma dose. The resultant effect of gamma irradiation on the properties of polyimide/silica nanocomposite has been investigated using X-ray diffraction and UV spectroscopy. Absorption and reflectance spectra were collected by a spectrophotometer giving UV-radiation of wavelength range 200–800?nm. The optical data obtained were analyzed and the calculated values of the optical energy gap exhibited gamma dose dependence. The direct optical energy gap for the nonirradiated polyimide/silica nanocomposite is about 2.41?eV, and increases to a value of 2.65?eV when irradiated with gamma doses up to 300?kGy. It was found that the calculated refractive index of the polyamide/silica increases with the gamma dose in the range 50–300?kGy.     

Gamma induced changes in the structural and optical properties of Makrofol LS 1–1 polycarbonate

ABSTRACT

Samples from sheets of the polymeric material Makrofol LS 1–1 have been exposed to gamma radiation in the dose range 10–250?kGy. The modifications induced in Makrofol samples due to gamma irradiation have been studied through different characterization techniques such as intrinsic viscosity as a measure of the average molecular mass, Fourier Transform Infrared spectroscopy FTIR, refractive index and color difference studies. The results indicate that the crosslinking dominates at the dose range 50–250?kGy. The crosslinking reported by viscosity measurements is supported by the trend of the function groups present in the sample with the gamma dose. Also, the increase in intrinsic viscosity indicating an increase in the average molecular mass was associated with an increase in the refractive index. Additionally, the non-irradiated Makrofol samples showed significant color sensitivity towards gamma irradiation. The color intensity ΔE, which is the color difference between the non-irradiated sample and those irradiated with different gamma doses, increased (0–5.56) with increasing the dose up to 250?kGy, convoyed by an increase in the red and yellow color components.     

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.     

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.     

Modifications induced by gamma irradiation upon structural,optical and chemical properties of polyamide nylon-6,6 polymer

The effects of gamma rays were studied on the optical, structural and chemical properties of the PA-66 polymer samples. The polymer samples obtained from Goodfellow (Cambridge, UK) were irradiated with gamma rays at various doses ranging from 100 to 1250 kGy. The pristine and gamma rays irradiated samples were characterized by UV–visible (UV–VIS) spectroscopy, X-ray diffraction (XRD) and Fourier transform infrared (FTIR) spectroscopy. UV–VIS shows a shift in absorption toward the visible region for irradiated samples and a decrease in band gap energy (E_g). The XRD analyses show an increase in the crystalline nature of the polymer at higher doses as a result of significant decrease in the peak width of XRD patterns. The FTIR spectra show decrease in intensity and shift of various bands with increase in gamma dose.     

Effect of gamma irradiation on the structural and optical properties of PVA/CdS nanocomposite films prepared by ex-situ technique

ABSTRACT

For a comprehensive understanding of the PVA/CdS nanocomposite properties, it is essential to select the suitable method for their preparation as well as elucidate the interfacial interactions, which still need support. CdS nanoparticles have been prepared by thermolysis method under the flow of nitrogen. Rietveld refinement of x-ray data shows that all the CdS samples have both cubic and hexagonal structures. Then PVA/CdS films were prepared by ex-situ technique. Samples from PVA/CdS nanocomposite have been irradiated with gamma doses in the range 10–120?kGy. The implanting of CdS NPs into PVA matrix was confirmed by XRD hand in hand with UV–vis and FTIR spectroscopic techniques. UV/VIS absorption spectra confirm the formation of hybridized film CdS/PVA nanocomposite with a refractive index in the range of 1.32–1.48 (at 500?nm). UV/VIS measurements were also used in calculating different optical parameters such as refractive index, extinction coefficient and optical band gap energy. Additionally, Tauc’s relation was used to determine the type of electronic transition. It is found that the gamma irradiation in the dose range 30-90?kGy led to a more compact structure of PVA/CdS nanocomposite and causes proper dispersion of CdS nanoparticles in the PVA matrix. This led to the formation of coordination reaction between OH of PVA and CdS nanoparticles, resulted in an increase in refractive index and the amorphous phase. Also, the gamma irradiation reduces the optical energy gap from 4.53 to 2.19?eV, and accompanied with an increase in the Urbach energy from 2.28 to 4.46?eV, at that dose range which could be attributed to the increase in structural disorder of the irradiated PVA/CdS nanocomposites due to crosslinking. Further, the color intensity ΔE, which is the color difference between the non-irradiated sample and the irradiated ones, was increased, from 0 to 10.8, with increasing the gamma dose, convoyed by an increase in the red and yellow color components.     

The Chain Segment Motion and Traps in γ‐Irradiation Crystalline Nylon 1010

The chain segment motion, charge trapping and detrapping in γ‐irradiated nylon 1010 films (doses in the range 0–2,000 kGy were used) have been investigated by means of thermally stimulated depolarization current (TSDC). There are three current peaks (named α, ρ₁ and ρ₂, respectively) in the TSDC spectra, corrected by spontaneous current, above room temperature. By analyzing the characteristic parameters of the three peaks, it is found that the chain segment motion in the amorphous regions becomes more difficult at low irradiation dose (<100 kGy) and then becomes easier with further increasing irradiation dose. The stability of the traps at the crystalline‐amorphous interfaces increases at low irradiation dose (<500 kGy) and then decreases with further increasing irradiation dose; the irradiation promotes the creation of traps and the stability of traps in the crystalline regions.     

Optical and electrical properties of swift heavy ion beam-irradiated polycarbonate/polystyrene bilayer films

Polycarbonate/polystyrene bilayer films prepared by solvent-casting method were irradiated with 55 MeV carbon ion beam at different fluences ranging from 1×10¹¹ to 1×10¹³ ions cm^?2. The structural, optical, surface morphology and dielectric properties of these films were investigated by X-ray diffraction (XRD), UV–visible spectroscopy, Fourier-transform infrared (FTIR) spectroscopy, optical microscopy and dielectric measurements. The XRD pattern shows that the percentage of crystallinity decreases while inter-chain separations increase with ion fluence. UV–visible spectroscopy shows that the energy band gap decreases and the number of carbon atoms in nanoclusters increase with the increase in ion fluences. The refractive index is also found to decrease with the increase in the ion fluence. Optical microscopy shows that after irradiation polymeric bilayer films color changes with ion fluences. The FTIR spectra evidenced a very small change in cross-linking and chain scissoring at high fluence. Dielectric constant decreases while dielectric loss and AC conductivity increase with ion fluences.     

Molecular and optical modifications in poly(vinyl chloride) due to N-phenylmaleimide additives and gamma irradiation

The effects of N-phenylmaleimide (NPMI) concentration and gamma dose on the molecular and optical properties of poly(vinyl chloride) (PVC) have been studied. The results reveal an improvement in the intrinsic viscosity of PVC in the presence of an organic material. The effective concentration that enhanced the intrinsic viscosity, from 1.02 to 1.28, was found to be 10 mmol NPMI per 100 g PVC. The effect of gamma irradiation on the PVC polymer stabilized with this concentration of NPMI has been studied. Samples from the 0.01 g NPMI/1 g PVC were irradiated with gamma doses in the range 5–180 kGy. It is found that irradiation in the dose range 120–180 kGy enhances the intrinsic viscosity of the samples. In addition, the transmission of these irradiated samples in the wavelength range 200–2500 nm, as well as any color changes was studied. The color intensity (Δ E) was greatly increased with the increasing gamma dose, and was accompanied by darkness with a significant increase in the yellow color component.     

Electron beam induced modifications in conductivity and dielectric property of polymer electrolyte film

This paper describes the effect of 8 MeV of electron beam (EB) energy irradiation on the electrical conductivity and dielectric properties of sodium fluoride NaF-doped polyethylene oxide (PEO) film. The structural and chemical characterizations were employed using X-ray diffractometry (XRD) and Fourier Transform Infrared (FTIR) techniques respectively before and after irradiation. The morphology study carried out using Scanning Electronic Microscopy (SEM) analysis. The DC electrical conductivity showed increases with dose and temperature and was consistent with Arrhenius behavior. The maximum conductivity of 1.1 × 10⁻⁵ S/cm and minimum activation energy of 0.25 eV were obtained at 25 kGy, 338 K; further increases in the dose resulted in a reduction in conductivity. The real (ε′) and imaginary (ε″) part of the dielectric constant suddenly decreased in a low frequency region (40–640 Hz), subsequently independent at higher frequency. The AC conductivity showed increases with frequency and temperature for all films. The dielectric constant and AC conductivity increased at the 25 kGy dose due to chain scission. Further increases in dose such as 50 and 75 kGy, resulted in a decrease in dielectric constant and AC conductivity due to cross-linking. The electric modulus approach was used to calculate the dielectric relaxation time (τ), which decreased at 25 kGy and then increased at 50 and 75 kGy doses. The modulus data were fitted using a non-exponential Kohlrausch–Williams–Watts (KWW) function ϕ (t), and the results indicate the existence of a non-Debye relaxation.