Addition of Transition Metals to Improve Physico-Mechanical Properties of Radiation-Vulcanized Natural Rubber Latex Films

The effect of transition metals as a promoter of physico-mechanical properties of radiation-vulcanized natural rubber latex (RVNRL) films was investigated. RVNRL films were prepared by the addition of transition metals (Fe, Mn, etc.) of different concentrations (0–30 ppm) in natural rubber (NR) latex and irradiated with various radiation doses (0–20 kGy). The concentrations of metal ions and radiation doses were optimized and found to be 20 ppm and 12 kGy, respectively. Tensile strength, tear strength, and cross-linking density of the irradiated rubber films were increased with increasing concentration of metal ions as well as radiation doses. The mechanical properties of the films were enhanced by approximately 20% at the optimum conditions. In contrast, elongation at break, permanent set, and swelling ratio of the films were decreased under the same conditions. The comparative effect of metal ions can be explained by Fajan's rules, reported in this article.     

Effect of Manganese on Radiation Vulcanization of Natural Rubber

Manganese was added as a promoter to investigate physico-mechanical properties of radiation-vulcanized natural rubber latex (RVNRL) films. RVNRL films were prepared by the addition of Mn with the concentration range 0–30 ppm to natural rubber latex and irradiated with various radiation doses (0–20 kGy). Tensile strength, tear strength, and cross-linking density of the irradiated rubber films increased with increasing the concentration of Mn ions as well as radiation doses. In contrast, elongation at break, permanent set, and swelling ratio of the films were decreased under the same conditions. The concentration of Mn ions and radiation doses were optimized and found to be 20 ppm and 12 kGy, respectively. The maximum tensile and tear strengths of irradiated rubber films were observed as 29.12 MPa and 44.78 N/mm, respectively at the optimum conditions. The mechanical properties of the films increased markedly with the addition of Mn until they attained the highest values of 33.88 MPa and 54.77 N/mm, respectively. These enhancements, which reached approximately 20% at the most favorable conditions, can be explained by the effect of transition metals in view of Fajan’s rules regarding the covalent character of ionic bonds and suggest that the higher the difference in charges between cation and anion, the higher the ability to form distortion or polarization of ions.     

Role of Divalent Metals in Polymer Degradation

The role of divalent metals in the degradation of the physico-mechanical properties of radiation-vulcanized natural rubber latex (RVNRL) films was investigated. RVNRL films were prepared by the addition of metals (Cu, Mg, etc.) of different concentrations (0–30ppm) to natural rubber latex and irradiated with various radiation doses (0–20kGy). The radiation doses were optimized (12kGy), and the adverse effect of metal ions was studied against a reference film prepared with no metal ions. Tensile strength, tear strength, and cross-linking density of the irradiated rubber films decreased with increasing metal ion concentrations and decreasing radiation doses. The mechanical properties of the films were reduced by 10–15% for 30ppm metal ions and at the optimum dose. In contrast, elongation at break, permanent set, and swelling ratio of the films increased at the same conditions. The relative effect of metal ions can be explained by the classical electron concept, reported in this article.     

Gamma-Irradiated Gelatin-Based Films Modified by HEMA for Medical Application

The present article describes the synthesis and characterization of bi-component polymer systems based on gelatin films incorporated with 2-hydroxyethyl methacrylate (HEMA) monomer, developed for medical application. Gelatin films were prepared by the addition of HEMA of different concentrations (0–30 wt.%) and irradiated with various radiation doses (0–5 kGy). Tensile strength and tear strength of the irradiated gelatin films were found to increase with increasing HEMA up to 20 wt.% as well as radiation doses (1 kGy) as optimized. The maximum tensile and tear strengths of irradiated gelatin films with HEMA were found to be 79.1 MPa and 83.2 N/mm, respectively, at the optimum conditions, and these values were about double that of a reference film prepared without additives. In addition, morphological analysis was done by scanning electron microscopy (SEM) and showed how HEMA cemented and was covered with gelatin in the blend. Thermomechanical analysis was carried out to investigate the shifting of glass transition temperature (T_g) towards higher temperature due to HEMA addition, and the effect of this film was tested on the human body in order to determine whether it can be applied for medical purposes.     

Studies on radiation grafting of methyl methacrylate onto natural rubber for improving modulus of latex film

Methyl methacrylate (MMA) can be grafted onto natural rubber (NR) in latex by gamma irradiation for improving the mechanical properties of the dry films. Physical blending of MMA-grafted NR latex with radiation vulcanized natural rubber latex (RVNRL) or simultaneous radiation grafting and crosslinking are found to be useful techniques for improving the properties of latex films. Moduli of the films are improved with increasing MMA content; however, tensile strength is reduced. High modulus without much reduction in tensile strength can be achieved if the MMA content is 50–60 parts per hundred rubber.     

Fabrication and characterization of gamma-irradiated recycled (thermoplastic/elastomer) matrix filled with feldspar composites

A composite of waste polyethylene, recycled waste rubber powder and reactive compatibilizing agent maleic anhydride, 60/40/2 mass%, was loaded with increasing contents, up to 20 mass%, of the reinforcing filler, feldspar [K (Al SiO₃O₈)]. The composites were gamma-irradiated at various doses up to 150 kGy. Selected physical, mechanical, and thermal parameters were investigated as functions of radiation dose and filler content. Gamma irradiation led to a significant improvement in the properties for all composites irradiated with 150 kGy. Similarly, the increase in feldspar content provided substantial improvement in properties as a result of development in the interfacial adhesion between the filler particles and composite components. The results were confirmed by examining the fracture surfaces using scanning electron microscopic techniques.     

Radiation-assisted synthesis of iridium and rhodium nanoparticles supported on polyvinylpyrrolidone

The controlled synthesis of rhodium (Rh) and iridium (Ir) nanoparticles was carried out by gamma irradiation of aqueous solutions containing the metal precursor salt and polyvinylpyrrolidone (PVP). The nanoparticles were synthesized at various PVP and precursor concentrations with absorbed doses between 20 and 60 kGy. Nanoparticles with average sizes of 2.4 and 2.6 nm and narrow particle size distributions were obtained at metal precursor/PVP concentrations of 6/0.3 and 6/3 mM for Ir and Rh when irradiated at 60 kGy. The interaction of the nanoparticles surfaces with the PVP was studied.     

The sensitizing effect of acrylates on radiation vulcanization of natural rubber latex

The sensitizing effect of acrylates on radiation vulcanization of natural rubber latex was studied. The results indicate that Gc value of crosslinking (Gc) will be higher at the same radiation dose when a sensitizer exists, and Gc value decreases with the increase of radiation dose (D) conforming to the formula Gc=KD^-α, where K and α are constants depending on sensitizers. The more sensitizers added, the greater the Gc value. However, the viscosity of the natural rubber latex also increases rapidly along with the increase of sensitizers added.Some sensitizers, such as TMPTA, can decrease the optimum dose from about 200 kGy to approximately 20 kGy according to our experiment. The tensile strength of the film can reach round 20 MPa. Other physical properties are comparable to those of unsensitized.     

Ammonia Decomposition Using Electron Beam

This study was carried out to determine the decomposition characteristics of ammonia using an electron beam (EB). Factors influencing these decomposition characteristics such as background gases (air, N₂, O₂, and He), initial ammonia concentration (50–150 ppm), relative humidity (0 or 90 %), and absorbed dose (1–15 kGy) were investigated. In the results of removal characteristics by different background gases, the decomposition efficiency of ammonia was lower (approximately 45 % at 5 kGy) when He was used as a background gas compared to the efficiencies when other background gases were selected. Ammonia removal efficiencies, when initial concentrations were 50 and 150 ppm, were 95 and 75 %, respectively, at 15 kGy. Ozone generation by EB irradiation increased from 2.5 kGy and reached a maximum of 45 ppm when 5 kGy of the absorbed dose was irradiated. However, ozone generation started to decrease when the absorbed dose exceeded 5 kGy and decreased to 0.27 ppm at 15 kGy.     

Radiodegradation of nadolol in the solid state and identification of its radiolysis products by UHPLC–MS method

Nadolol ((2R*,3S*)-5-{[(2R*)-3-(tert-butylamino)-2-hydroxypropyl]oxy}-1,2,3,4 tetrahydronaphthalene-2,3-diol) in substantia was exposed to ionizing radiation generated by a beam of high-energy electrons in an accelerator, in the standard sterilisation dose of 25 kGy and in higher doses of 50 ? 400 kGy. The irradiated and non-irradiated (control) samples were analysed by the infrared spectrophotometry, electron paramagnetic resonance, differential scanning calorimetry (DSC) and ultra-high performance liquid chromatography coupled with mass spectrometry (UHPLC–MS). The irradiated samples were found to contain free radicals in concentrations much higher than that observed for the other irradiated β-blockers. On the basis of UHPLC–MS results, it was possible to establish structures of 11 compounds of the impurities and/or products of nadolol decomposition. The main product of radiodegradation was concluded to be formed as a result of abstraction of the hydroxyl group and aromatization of the tetrahydronaphthalene ring. The results of DSC measurements confirmed the presence of radiolysis products in the irradiated samples of nadolol. A shift of the endothermic peak corresponding to melting towards lower temperatures (by 4.4 °C at the dose of 400 kGy) was directly proportional to the doses of radiation used, which permits concluding that this method is sensitive and suitable for evaluation of radiodegradation of nadolol in solid phase.     

STUDY ON THE PROPERTIES OF BLEND OF NATURAL RUBBER LATEX/METHYL METHACRYLATE GRAFTED RUBBER LATEX BY GAMMA RADIATION

Natural rubber latex(NRL)and methyl methacrylate(MMA)grafted rubber latex were blended in different ratios and irradiated at various absorbed doses by gamma rays from Co-60 source at room temperature.The tensile properties, swelling ratio and permanent set were measured.The maximum tensile strength and modulus at 500% elongation were obtained at an absorbed dose of 8 kGy.Modulus increases from 6.99 MPa to 9.87 MPa for an increase in proportion of MMA grafted rubber from 40% to 60% in the blend at similar absorbed dose.Elongation at break and swelling ratio decrease with increasing absorbed dose as well as the MMA grafted rubber content in the blends.The decreasing trend of permanent set is high up to 5 kGy absorbed dose,and beyond that dose,it becomes almost flat.     

A STUDY ON RADIATION CROSSLINKING OFPOLYDIMETHYLSILOXANE （PDMS） RUBBER LATEX

Polydimethylsiloxane (PDMS) rubber latex with two sorts of sensitizers, trimethylol propane tri-methacrylate (TMPTMA) and diethylene glycol di-acrylate (DEGDA), was irradiated with y-rays and electron beams in various conditions. The radiation crosslinking reaction of PDMS occurs in the inner phase of the latex and is relatively isolated from the water phase. Therefore the oxygen and the radicals produced by the radiolysis reaction of water almost have no effect on the crosslinking reaction of polymer. The experimental data correspond with the Charlesby-Pinner relationship in the main. The gelation doses, degree of crosslinking and degradation as well as G values of crosslinking were calculated. From them, the sensitization coefficients were derived to offer a quantitative measurement of the enhancing effect of sensitizer on the radiation crosslinking.     

Analytical study on irradiated methylxanthine derivatives

The effect of ionising radiation on the physico-chemical properties of three derivatives of xanthine: caffeine, theophylline and theobromine, has been studied. The above-drugs in the solid phase have been irradiated with E-beam of the energy 9.96 MeV with the doses varied from 25 to 400 kGy. The effects of the irradiation have been examined by differential scanning calorimetry (DSC), electron paramagnetic resonance (EPR) and high-performance liquid chromatography (HPLC). The results have shown that the methylxanthine derivatives studied are resistant to ionising irradiation in the doses usually used for sterilisation (<50 kGy), which means that they are relatively radiochemically stable and can be sterilised by irradiation.     

Gamma radiation effects on molecular characteristic of vegetable tannins

The influence of gamma radiation on tannins extracted from Pinus caribaea bark and on tannin acid has been investigated in this study with the aim of searching for evidences of structural and/or conformational changes. To fulfill this purpose, the samples of tannins, such as tannic acid and P. caribaea tannin bark, were irradiated at different doses (from 5 to 35 kGy) using a cobalt-60 gamma irradiator. The changes were analyzed by a Fourier transform infrared spectrometry and by high resolution liquid chromatography. The results pointed out some structural and conformational changes under the effects of gamma radiation for doses higher than 5 kGy for P. caribaea tannin bark. However, no changes were detected on the irradiated tannic acid. The observed behavior suggests the loss of carbonyl groups. This could be associated to a decarboxylation process with the corresponding release of CO₂ from the molecule. Evidences of some conformational changes were also noted.     

The effect of gamma irradiation on mechanical, and thermal properties of recycling polyethylene terephthalate and low density polyethylene (R-PET/LDPE) blend compatibilized by ethylene vinyl acetate (EVA)

A study has been made on the compatibility of recycled polyethylene terephthalate (R-PET) and low density polyethylene (LDPE) blend in the presence of ethylene vinyl acetate (EVA) as a compatibilizing agent prepared by extrusion hot stretching process. EVA content in the blend as a compatibilizing agent was an enhancement effect on radiation crosslinking of R-PET/EVA/LDPE blends and the highest radiation crosslinking was obtained when the EVA content was reached at 10 % EVA when irradiated by gamma irradiation. Blends containing different (EVA) ratios were irradiated to different doses of gamma irradiation 25, 50 and 100 kGy. The effect of the compatibilizer and radiation on mechanical, thermal properties of R-PET together with LDPE and morphology has been investigated. It was found that gamma irradiation together with the presence of compatibilizing agent (EVA) has positive effect on the mechanical and thermal properties of R-PET/LDPE blend. The structural properties of R-PET/LDPE modified by gamma irradiation and EVA as compatibilizing agent was examined by SEM. Also, it was found that the optimum concentration of EVA and gamma irradiation dose was found to be 10 % EVA and 100 kGy, respectively.     

Effect of gamma radiation on the physico-chemical properties of alginate-based films and beads

Alginate solution (3%, w/v) was prepared using deionized water from its powder. Then the solution was exposed to gamma radiation (0.1?25 kGy). The alginate films were prepared by solution casting. It was found that gamma radiation has strong effect on alginate solution. At low doses, mechanical strength of the alginate films improved but after 5 kGy dose, the strength started to decrease. The mechanism of alginate radiolysis in aqueous solution is discussed. Film formation was not possible from alginate solution at doses >5 kGy. The mechanical properties such as puncture strength (PS), puncture deformation (PD), viscoelasticity (Y) coefficient of the un-irradiated films were investigated. The values of PS, PD and Y coefficient of the films were 333 N/mm, 3.20 mm and 27%, respectively. Alginate beads were prepared from 3% alginate solution (w/v) by ionotropic gelation method in 5% CaCl₂ solution. The rate of gel swelling improved in irradiated alginate-based beads at low doses (up to 0.5 kGy).     

Fabrication and mechanical characterization of biodegradable and synthetic polymeric films: Effect of gamma radiation

Chitosan (1 wt%, in 2% aqueous acetic acid solution) and starch (1 wt%, in deionised water) were dissolved and mixed in different proportions (20–80 wt% chitosan) then films were prepared by casting. Tensile strength and elongation at break of the 50% chitosan containing starch-based films were found to be 47 MPa and 16%, respectively. It was revealed that with the increase of chitosan in starch, the values of TS improved significantly. Monomer, 2-butane diol-diacrylate (BDDA) was added into the film forming solutions (50% starch-based), then casted films. The BDDA containing films were irradiated under gamma radiation (5–25 kGy) and it was found that strength of the films improved significantly. On the other hand, synthetic petroleum-based polymeric films (polycaprolactone, polyethylene and polypropylene) were prepared by compression moulding. Mechanical and barrier properties of the films were evaluated. The gamma irradiated (25 kGy) films showed higher strength and better barrier properties.     

Radiation immobilization of poly(methyloctylsiloxane) on silica for use in HPLC: a uniform layer model.

Poly(methyloctylsiloxane) (PMOS) was sorbed into the pores of HPLC silica by a solvent evaporation procedure, then irradiated with gamma rays from a cobalt-60 source to absorbed doses in the range from 0 to 200 kGy (1Gy = 1J kg-1). Non-irradiated and irradiated samples were characterized by solvent extraction, specific surface area determination, infrared spectroscopy and reversed-phase column performance. Solvent extraction data reveal that about 40% of the PMOS is not extractable prior to irradiation and this increases to about 75% with radiation doses of 50 kGy or higher. Column performance was improved by the radiation treatment, reaching a maximum efficiency in the dose range of 80-140 kGy while the peak symmetry changed from As = 1.7 to 1.1. The improvement is attributed to the increased mass of polymer immobilized by the radiation treatment and to a more uniform distribution of the immobilized polymer in the silica pore system. A multi-layer stationary-phase model is presented in which the first layer consists of an adsorbed monolayer of PMOS and the second layer is immobilized by gamma radiation.     

Potential use of the activation energy value calculated from the thermoluminescence glow curves to detect irradiated food

We herein report on the calculation of the activation energy (E _a) from the thermoluminescence (TL) glow curves performed by the initial rise method that allows us to discriminate between irradiated and non-irradiated sesame seeds. E _a values of natural TL (0.68 ± 0.03 eV) and gamma-induced TL (never lower than 0.82 ± 0.02 eV) appear as a complementary criterion to be used differentiating between irradiated and non-irradiated foodstuffs with the position and the intensity of the main peak of the TL emission. In addition, E _a values taken from irradiated sesame samples at different doses (1, 5 and 10 kGy) and stored up to 15 months after being processed were compared to a ‘positive’ Spanish blend (i.e. at least one component was commercially irradiated).     

Gamma irradiation of protein-based textiles for historical collections decontamination

In order to investigate the effect of gamma rays on cultural heritage materials, samples of silk and wool fabrics were subjected to accelerated ageing testing and then irradiated with different gamma-ray doses: 10 and 25 kGy. In the data analysis, combining thermal analysis (TG and DTG), infrared spectroscopy (FTIR-ATR) and mechanical tests allowed us to explore the changes in physical and chemical features for silk and wool, in relationship to the radiation doses. This analytical protocol offers a way to examine the behaviour of the textiles made of wool and silk within museum collections and their response to gamma-rays irradiation treatment. An exposure to a dose of 10 kGy did not cause significant changes in the tested properties; however, higher doses initiated irreversible loss in the physical and chemical stability of protein-based fabrics. Increasing the irradiation dose above 10 kGy has drastic effects in the loss of elasticity and the mechanical resistance of the tested yarns.