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.     

Proton-induced changes in Bayfol CR 1-4 nuclear track detector

Samples from the polymeric material Bayfol CR 1-4 have been exposed to 1 MeV protons with fluencies in the range 10¹¹–10¹⁴ ions/cm ². The resultant effect of proton irradiation on the thermal properties of Bayfol CR 1-4 has been investigated using thermo-gravimetric analysis (TGA). The onset temperature of decomposition T ₀ and activation energy of thermal decomposition E _a were calculated, results indicated that the Bayfol detector decomposes in one weight loss stage. In addition, the structural modifications in the proton-irradiated Bayfol samples have been studied as a function of fluence using X-ray diffraction and intrinsic viscosity of the liquid samples. Furthermore, the refractive index was measured for the non-irradiated and irradiated Bayfol samples. The results indicated that the degradation is the dominant mechanism in the fluence range 1×10¹¹–5×10¹⁴ ions/cm ². These results have been compared with those obtained in our previous work for Bayfol CR 6-2.     

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.     

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.     

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.     

Structural modifications induced in Bayfol polycarbonate due to heavy highly energetic ions irradiations

The effects of 28 GeV ⁵⁶Fe and 13.72 GeV ²⁸Si ion irradiation on the structural properties of two types of Bayfol, namely DPF 5023 and CR 1–4 polycarbonates, have been investigated. It is worth mentioning that this report is almost the first one dealing with the topic of material changes in such a high energy range. Samples from each type of Bayfol were classified into two groups. The first group has been exposed to Fe ion fluences at levels between 2000 and 8000 ion/cm². The second group has been exposed to Si ions with similar fluences. The total energy deposited is between 27.44 and 224 E12 eV. The modifications induced in Bayfol samples due to ion irradiation have been studied using X-ray diffraction (XRD) and Fourier Transform Infrared spectroscopy. The results indicate that the Fe ion irradiation causes crosslinking in Bayfol DPF 5023, reflected as a decrease in the ordering character. Also, the tendency of Bayfol CR 1–4 to crosslinking due to Fe ion irradiation is lower than that of Bayfol DPF 5023. On the other hand, the Si ion irradiation causes mainly chain scission at the carbonate site of both types of Bayfol associated with the formation of hydroxyl group.     

X-ray irradiation-induced structural modifications in PM-355 polymeric nuclear track detector film

Samples from sheets of the polymeric material PM-355 have been exposed to X-rays from a 50 kV X-ray tube in the dose range of 10–300 kGy. The resultant effect of X-ray irradiation on the structural properties of PM-355 has been investigated using different techniques such as X-ray diffraction (XRD), Fourier transform infrared (FTIR) spectroscopy, Vickers hardness and refractive index measurements. The results indicate that the X-ray irradiation of PM-355 in the dose range of 10–20 kGy causes initially chain scission. Above 20 and up to 100 kGy, the active free radicals produced from scission contribute to chemical reactions that lead to the crosslinking. Thus, the X-ray irradiation in the dose range of 20–100 kGy leads to a more compact structure of the PM-355 polymer, resulting in an enhancement of its Vickers hardness and refractive index. Moreover, the irradiation in the dose range of 100–300 kGy leads to the predominance of the degradation. This degradation is reported by FTIR spectroscopy and enhances the degree of ordering in the degraded samples as revealed by XRD technique. Additionally, it decreases both the Vickers hardness and refractive index of the PM-355 samples.     

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.     

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.     

Gamma radiation effects on mechanical properties and morphology of a polyurethane derivate from castor oil

In this study, an adhesive of a polyurethane derivate from castor oil was irradiated with gamma radiation from a ⁶⁰Co source, at doses from 0.2 to 25 kGy. This adhesive polyurethane is considered for use in hospital furniture because it does not liberate dangerous solvents. Hardness and elastic modulus were measured by instrumented indentation with a pyramidal Berkovich indenter, using loads from 0.08–40 mN with a nanoindenter XP. The instrumented indentation hardness was 110 MPa for an untreated sample, increasing to 124 MPa after irradiation with 25 kGy, at penetration depths of about 5 μm. The increases in elastic modulus induced by radiation were less pronounced. This polyurethane is naturally cross-linked and the relative modifications in the hardness are attributed to an additional cross-linking process induced by radiation. X-ray diffraction indicates a slight increase in crystallinity. The roughness measured by atomic force microscopy increases after 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.     

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.     

Effect of gamma irradiation on HPMC/ZnO nanocomposite films

The present work looks into the structural, chemical, mechanical, optical and thermal modification in ZnO nanoparticle incorporated hydroxypropyl methylcellulose (HPMC) polymer films, induced by gamma irradiation. The irradiation process was performed in a gamma chamber at room temperature using Cobalt-60 source (average energy of 1.25?MeV) at different doses: 0, 50, 100, 150 and 200?kGy. The modifications in structural, chemical, mechanical, optical and thermal properties, due to gamma irradiation in HPMC/ZnO nanocomposite films, have been studied using wide angle X-ray scattering (XRD), Fourier transform infrared spectroscopy, universal testing machine, ultraviolet–visible spectrophotometry and thermogravimetric analysis. It is found that gamma irradiation improves the mechanical and thermal properties of nanocomposite films.     

Effect of gamma irradiation on hydrothermally synthesized barium titanate nanoparticles

The effect of gamma irradiation on hydrothermally synthesized BaTiO₃ nanoparticles has been investigated. Gamma irradiation was carried out at room temperature from 0, 50, 100, 150, 200?kGy to a maximum dose up to 250?kGy, source being ⁶⁰Co gamma radiations. The structure, size and chemical changes of the BaTiO₃ were studied using X-ray diffraction, Fourier-transform infrared spectrophotometry (FTIR) techniques and scanning electron microscopy (SEM). The optical band gap has been computed by UV–Visible spectroscopy data. From the results obtained, it is evident that the gamma irradiation increases the crystallinity, whereas the particle size of BaTiO₃ nanoparticles is altered. UV–Visible spectroscopy shows a noticeable change in the energy band gap due to gamma irradiation. Significant changes in anharmonicity constant computed using FTIR data due to irradiation has been observed. SEM shows the size and deviation from uniformity of particles.     

Gamma-irradiation effect on a commercial composite anticorrosive pigment and acidity-to-alkalinity conversion

A commercial composite anticorrosive pigment based on aluminum dihydrogen tripolyphosphate was studied after exposure to gamma irradiation (Co⁶⁰, 0, 20, 50, 100 and 150?kGy) using FTIR, XRD, TGA and acid-base titration technologies. Although the FTIR spectra showed that the effect of the irradiation on functional groups in the pigments was not obvious, the decrease in the crystal lattice parameters of the irradiated pigments was observed in the XRD spectra compared to the non-irradiated sample. But the extent of the lattice parameter decrease monotonically with the increase of absorbed dose from 20 to 150?kGy, which was attributed to the decomposition of water and the simultaneous occurrence of lattice damage when the pigments were exposed to gamma rays. Of particular significance was the displayed basicity of the aqueous solutions of the irradiated pigments compared to the acidity of the solution of the non-irradiated pigment, which was attributed to the decomposition of P-OH groups (combined water).     

Structural,electrical and optical properties of gamma irradiated methyl para-hydroxy benzoate single crystals

ABSTRACT

Nonlinear optical materials (NLO) have been garnering attention due to their role in optical data storage, optical communication and laser technology. Organic crystals have emerged as an extremely important class of NLO materials, since their NLO properties compare very well with traditional inorganic NLO materials like KCl, LiNbO₃, KDP (potassium dihydrogen phosphate), etc. They offer the additional advantage that they can be grown relatively inexpensively from solution close to room temperature, unlike the inorganic NLO materials which are grown from high temperature melts. In the present work, organic transparent single crystals of methyl para-hydroxy benzoate (MHB) were grown by slow evaporation solution growth technique (SEST) from aqueous solution at room temperature. The changes in structural, electrical and optical properties of gamma irradiated MHB single crystals were studied using X-ray diffraction (XRD), UV–Visible absorption spectroscopy, Photo-luminescence (PL), Fourier transform infrared (FTIR) spectroscopy and AC conductivity measurements at room temperature. The polished MHB single crystals were irradiated with gamma rays of doses 10 and 15 kilogray (kGy). From the XRD analysis, it was observed that gamma irradiation for these doses drastically decreases the crystallinity. The optical absorption constants were examined by UV-Visible absorption spectroscopy, measured over the wavelength range of 200–800?nm, at normal incidence. The optical band gap as estimated from the Tauc plot ((αhν)² vs hν) was found to be reduced with increasing gamma irradiation doses. PL spectra showed emission at wavelengths of 361?nm (3.43?eV) and 452?nm (2.74?eV), with enhanced intensities for the irradiated crystals. FTIR spectroscopy was utilised to identify the functional groups of MHB and indicated the rupture of specific types of bonds with gamma irradiation. Apart from that, the enhancement of AC conductivity with gamma irradiation was also observed for the gamma irradiated crystals.     

Electron-beam irradiation effects on poly(ethylene-co-vinyl acetate) polymer

Poly(ethylene-co-vinyl acetate) (EVA) films were irradiated with a 1.2 MeV electron beam at varied doses over the range 0–270 kGy in order to investigate the modifications induced in its optical, electrical and thermal properties. It was observed that optical band gap and activation energy of EVA films decreased upon electron irradiation, whereas the transition dipole moment, oscillator strength and number of carbon atoms per cluster were found to increase upon irradiation. Further, the dielectric constant, the dielectric loss, and the ac conductivity of EVA films were found to increase with an increase in the dose of electron radiation. The result further showed that the thermal stability of EVA film samples increased upon electron irradiation.     

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.     

Polydimethylsiloxane rubber gamma radiation effect studies by positron annihilation lifetime spectroscopy

Polydimethylsiloxane rubber was irradiated at various radiation doses up to 800 kGy in air. The lifetime and intensity of the long component τ₃ were obtained by positron annihilation lifetime spectroscopy (PALS). The crystallization property and the molecular flexibility were estimated using the differential scanning calorimetry and dynamic thermomechanic analysis. Thermal volatile property was determined by thermogravimetry analysis. It was proved that the cross-linking reaction made the chain flexibility of the rubber to reduce gradually during gamma radiation, which resulted in the reduction of the o-Ps intensity observed by PALS. Although the degradation effect existed during gamma radiation, it was still less significant than the cross-linking effect when the radiation dose was up to 800 kGy.