Mechanical response of high density polyethylene to gamma radiation from a Cobalt-60 irradiator

The response of High Density Polyethylene (HDPE) to gamma irradiation is important for a variety of applications, from the durability of hip replacements after gamma sterilization to the degradation of power cable insulation that guides the licensing and regulation of nuclear power plants. HDPE samples are irradiated with up to 58.8 kGy from a Cobalt-60 gamma irradiator, and mechanical properties are examined using models assuming exponential behavior. Increasing the radiation dose led to increases to the ultimate strength and the Rockwell hardness with a corresponding reduction in the maximum elongation at ultimate strength, supporting the hypothesis that the samples increased their strength and brittleness.     

Effects of gamma irradiation on chemical composition and ruminal protein degradation of canola meal

Gamma irradiation of canola meal (at doses of 25, 50 and 75 kGy) could alter its ruminal protein degradation characteristics by cross-linking of the polypeptide chains. This processing resulted in decrease (linear effect, P<0.001) of ruminal protein degradation and increase (linear effect, P<0.001) of intestinal protein digestibility. The results showed that gamma irradiation at doses higher than 25 kGy can be used as a cross-linking agent to improve protein properties of supplements in ruminant nutrition.     

γ‐Irradiation Degradation of Methamidophos

The irradiation degradation of methamidophos in aqueous solutions by ⁶⁰Co‐γ rays was investigated. The effects of absorbed doses, saturated gas, and the additive of H₂O₂ on the degradation were also studied. The results showed that the oxidative radical, such as ·OH, played an important role in the irradiation degradation of methamidophos; while the reductive radicals, e^?_aq and ·H, had no contribution to the degradation. The degradation rate of methamidophos increased with the increase of the irradiation dosage. At certain irradiation dosage, methamidophos could be degraded completely. The degradation rate of methamidophos in the solution saturated with oxygen was higher than those saturated with other gases, which reached 100% when the absorbed dose was 8 kGy. H₂O₂ degraded methamidophos slowly when it was used alone, but could accelerate the degradation obviously when it was used with irradiation together.     

Photo- and Radiation Creep and Durability of Polymers

The creep behavior of polycarbonate, polycaproamide, and polystyrene samples upon simultaneous and successive irradiation by fast electrons and optical-frequency radiation (photo- and radiation impact) was studied. The action of visible light in conjunction with electrons or immediately after electron irradiation leads to a dramatic increase in the creep rate. The absorbed doses of the onset of polymer degradation upon photo- and radiation impact are about an order of magnitude lower than those for electron irradiation alone. Macroradicals and stable radiolytic products absorbing light in a longer wavelength spectral region as compared with the initial polymers are assumed to be responsible for the photo- and radiation creep and durability of the polymers.     

Gamma-Irradiation-Induced Degradation of the Water-Soluble Polysaccharide from Auricularia polytricha and Its Anti-Hypercholesterolemic Activity

The water-soluble polysaccharides (APPs) isolated from the edible mushroom Auricularia polytricha were irradiated by γ-ray at doses of 10, 100, and 1000 kGy. The effect of gamma irradiation on the degradation of the polysaccharide was investigated. After irradiation treatment, the viscosity and molecular weight of APPs decreased with the increase in the irradiation dose. The changes in the enthalpy of APPs after irradiation treatment were observed. Meanwhile, SEM showed that R-APPs were crushed into fragments and the surfaces became smooth and wrinkled after irradiation. In further spectrum analysis, it was found that the glycoside bonds of the polysaccharides were broken and accompanied by the formation of double bonds. This suggested that gamma irradiation could cause the depolymerization and oxidation of polysaccharides. In addition, irradiated APPs could reduce the body weight of hyperlipidemia mice. The levels of serum and liver TC, TG, and serum LDH-c significantly decreased in hyperlipidemia mice after treatment by irradiated APPs. It indicated that gamma irradiation significantly improved the anti-hypolipidemic activity of APPs. The relationship between the physicochemical properties and hypolipidemic activity of polysaccharides was interpreted, which provides a theoretical basis for the further development of APP products. Gamma irradiation is a viable technology for macromolecular modification for degradation.     

Degradation behavior of poly (l-lactide-co-glycolide) films through gamma-ray irradiation

Gamma-ray irradiation is a very useful tool to improve the physicochemical properties of various biodegradable polymers without the use of a heating and crosslinking agent. The purpose of this study was to investigate the degradation behavior of poly (l-lactide-co-glycolide) (PLGA) depending on the applied gamma-ray irradiation doses. PLGA films prepared through a solvent casting method were irradiated with gamma radiation at various irradiation doses. The irradiation was performed using 60Co gamma-ray doses of 25–500 kGy at a dose rate of 10 kGy/h.The degradation of irradiated films was observed through the main chain scission. Exposure to gamma radiation dropped the average molecular weight (M_n and M_w), and weakened the mechanical strength. Thermograms of irradiated film show various changes of thermal properties in accordance with gamma-ray irradiation doses. Gamma-ray irradiation changes the morphology of the surface, and improves the wettability. In conclusion, gamma-ray irradiation will be a useful tool to control the rate of hydrolytic degradation of these PLGA films.     

Chemical, sensory and microbiological changes of gamma irradiated coconut cream powder

A study was carried out to determine optimum decontamination dose for a locally manufactured coconut cream powder. Samples were gamma irradiated (0–15 kGy) and ageing process was achieved using GEER oven at 60 °C for 7 days, which is equivalent to one-year storage at room temperature. Iodine value (IV), ranging from 4.8 to 6.4, was not affected by radiation doses and storage, however peroxide value and thiobarbituric acid (TBA) generally increased with radiation doses. In most samples, peroxide value (meq/kg) reduced after storage, whilst the TBA (mg malonaldehyde/kg), indicator for product quality, slightly increased. The sensory evaluation conducted using 25 taste panellists indicated that scores on odour, creamy taste and overall acceptance for all irradiated samples at more than 5 kGy were significantly lower (P<0.05) than the control. However, the panellists could not detect any significant differences among the irradiation doses (P>0.05). All stored products were significantly different in colour, creamy taste, odour and overall acceptance (P<0.05) when compared to the non-stored non-irradiated control. Microbiological count of the samples prior to irradiation was in the range of 1×10²–1.7×10³ cfu/g with no detection of Salmonella sp. and Escherichia coli. No microbial colonies were detected after irradiation. Based on the TBA and overall sensory acceptance, gamma irradiation of 5 kGy was found to be the optimum dose and lower doses can be considered to decontaminate coconut cream powder.     

Comparison of the efficacy of gamma and UV irradiation in sanitization of fresh carrot juice

As there is no pasteurization procedure for the manufacture of fresh vegetable juice, both industry and consumers have sought a method for improving the storage stability and shelf-life of this category of products. In this study, the effects of commercially available, non-thermal pasteurization processes, such as gamma and UV irradiation, were compared for their efficacy in sanitizing fresh carrot juice (FCJ). FCJ was manufactured, packaged, and gamma irradiated with doses of 0, 1, 3, and 5 kGy. The manufactured FCJ was also passed through 4 UV light lamps at doses of 3.67, 4.69, and 6.50 kGy. The total aerobic bacterial count of the FCJ approached the legal limit (10⁵ CFU/mL) after manufacturing. Both treatments were effective in reducing the number of total aerobic bacteria, and the reduced number was maintained during storage for 7 days. Gamma irradiation was more effective in suppressing microbial growth during storage. When the doses for UV treatment and gamma irradiation were higher, the inactivation effects were higher. The reduction of ascorbic acid content was greater upon gamma irradiation than UV treatment. No difference was found in the contents of flavonoids and polyphenols in FCJ after either treatment. After 3 days of refrigerated storage, the sensory scores of gamma- or UV-irradiated FCJ were superior to those of the control. The results indicate that both non-thermal treatments were effective in improving storage stability and extending shelf-life, but gamma irradiation was slightly better in suppressing microbial growth after treatment.     

Studies of the degradation of organotin stabilizers in poly(vinyl chloride) during gamma irradiation

Organotin stabilizers of the type Bu₂SnX₂ (X = SCH₂CO₂C₈H₁₇ or O₂CCH?CHCO₂C₈H₁₇) present in poly(vinyl chloride) (PVC) and subjected to varying doses of gamma irradiation in the range 1–200 kGy (0.1–20 Mrad) are shown to suffer degradation with dealkylation to form monobutyltin trichloride and tin(IV) chloride, which have been characterized by a subsequent alkylation procedure followed by gas chromatographic analysis. The extent of degradation of the stabilizers on prolonged gamma irradiation is much more severe than during thermal degradation leading to comparable blackening of the polymer.     

电子束辐照与电化学还原联用技术——一种用于煤炭直接液化的新方法

对电子束辐照与电化学联用技术提高煤炭液化率的新型方法进行了研究。利用高能电子束对煤炭样品进行辐照,并通过四氢呋喃萃取出辐照后的可能产物并计算其提取率。实验结果发现,提取产率随着辐照剂量的增加而增加,并得到在氧气气氛下25 kGy的最佳辐照条件。辐照的样品进一步在氢氧化钠电解液中电化学还原液化,并采用元素分析法、傅里叶红外光谱法、阴极极化曲线法、核磁共振法和计时电流法等来检测辐照对煤炭电化学还原的影响。     

Emanation thermal analysis of low-density polyethylene irradiated by electron beam

The thermal behaviour of low-density polyethylene (LDPE) as powder and pellet have been characterised by means of the emanation thermal analysis (ETA) during heating in air. The ETA was used in the study of LDPE polymer before and after irradiation to various doses of high energy electrons. It was shown that the ETA reflects microstructure changes taking place as the result of thermal degradation and oxidation pyrolysis of the polymer samples. It was shown in the study of LDPE products, resulting after the electron-beam treatment, that the results of ETA reflect structural changes caused by the radiation over the range of absorbed doses from 0 to 20 MGy. The annealing chemical radicals produced by the electron-beam irradiation was assessed by comparing ETA curves measured during first and second heating runs.     

Oxidation of benzalkonium chloride by gamma irradiation: kinetics and decrease in toxicity

The gamma degradation of toxic non-oxidizing biocide dodecyl dimethyl benzyl ammonium chloride (DDBAC) was investigated. The degradation of DDBAC achieved 70–100% depending on the initial concentration and the absorbed dose, but only 10–33% dissolved organic carbon was removed. The presence of NO₃ ^?, HCO₃ ^?, 2-propanol and tert-butanol inhibited the degradation of DDBAC. The DDBAC degradation rate constant ratios of ·OH, ·H and e _aq ^? was calculated as 7.4:1.4:1. The acute toxicity of 10 mg L^?1 DDBAC was removed by 60% at absorbed doses of 0.5–3.0 kGy. The results showed that gamma irradiation was effective to remove DDBAC and its toxicity.     

Effect of gamma irradiation on ethylene–octene copolymers

Two ethylene–octene copolymers (POE) were irradiated with ⁶⁰Co gamma radiation and influence of irradiation atmosphere, absorbed dose and heat treatment of samples on the crosslinking were studied. Thermal properties and crystalline morphology of non-irradiated and irradiated POE were determined by using differential scanning calorimetry (DSC) and wide-angle X-ray diffraction (WAXS), respectively. The Charlesby–Pinner equation was used to describe the relationship between absorbed dose and sol fraction. The gel fraction of irradiated POE was lower and decreased with the increase of octene content when irradiated in oxygen, compared to irradiation in nitrogen atmosphere. The gel fraction increased significantly with the increasing of absorbed dose for the two copolymers. Heat treatment of samples prohibited the crosslinking of irradiated POE. The DSC results indicated that a subtle change of thermal properties of POE was observed before and after gamma irradiation at low dose. No change was found from the WAXS spectra of non-irradiated and irradiated POE. For heat-treating samples, the Charlesby–Pinner equation can not fit perfectly with the relationship between the sol fraction and absorbed dose, but it fits well with the crosslinking reaction of POE pellets.     

Radiation modified high impact polystyrene

The purpose of applying high energy (ionising) radiation with absorbed doses up to 1 MGy was to achieve controllable changes in mechanical properties of high impact polystyrene (PS-HI) and, at the same time, to investigate the possibility of using reprocessed irradiated polymeric material. Dielectric relaxation of a radiation modified high impact polystyrene (PS-HI) has been investigated by the time dependence of charging and discharging current. The transient currents for the irradiated PS-HI were well approximated by the power function of the logarithm of time and related to the fractal dimension. It was also shown that yield strength and tensile strength increase while elongation at break decreases with increasing absorbed dose. The specimen prepared by a post-irradiation moulding gave higher melt flow rate than those of specimen formed before irradiation. These results indicate that after radiation the system of PS-HI is reprocessable. It is concluded that an oxygen environment at the beginning of irradiation leads to enhanced chain scission at the expense of crosslinks via peroxide formation and causes oxidative degradation of the main polymer chain of irradiated PS-HI at a low absorbed dose. However, at higher absorbed doses the quasi-inert environment has been established and crosslinking, due to recombination of macroradicals, is dominant.     

Investigation on the effects of beta and gamma irradiation on conducting polymers for sensor applications

Two conductive polymers were evaluated to be the active materials in a sensor device for the detection of beta radiation. This was accomplished by characterizing the changes in conductivity of electrically conducting polymer films caused by exposure to tritium gas for varying lengths of time. The behavior of these materials when exposed to gamma radiation was also studied to gain further insight into the mechanism of conductivity degradation by ionizing radiation. Two types of conductive polymer, polyaniline (PANi) and poly(3,4-ethylenedioxythiophene) (PEDOT), were chosen as candidate materials for their widespread commercial use. The change of surface resistance (conductivity) of PANi and PEDOT films when exposed to gamma radiation in both air and deuterium environments was evaluated as well as tritium exposures in 10⁴ and 10⁵ Pa gas. Raman and absorbance spectra of gamma irradiated samples were obtained to determine the mechanism of conductivity degradation in both polymers. Post-irradiation gas analysis of the samples contained in deuterium revealed very little (or no) hydrogen in the containment vessel, indicating that hydrogen–deuterium isotopic exchange was not responsible for the decrease in surface conductivity due to gamma exposure. The effects of irradiation-induced oxidation were also studied for both conductive polymers during gamma irradiation. It was concluded that chain scission via free radical formation and chain cross-linking are most likely the two dominant mechanisms for conductivity change and not de-protonation of the polymer.     

Thermogravimetric and calorimetric study of cellulose paper at low doses of gamma irradiation

The study of the behaviour of cellulose materials at low doses of ionizing radiation regained the interest because of the recent results showing that physical properties of the paper have less or no changes for absorbed doses below 10 kGy, despite the high decrease of the degree of polymerization. The understanding of the relationship among molecular, microscopic and macroscopic changes in cellulose materials may change the current opinion that irradiation of paper is not the best choice for conservation of cultural heritage. The aim of this study is to reveal the changes in gamma-irradiated pure cellulose paper by simultaneous TG/DSC analysis. For cellulose fibres, the thermal decomposition parameters depend on the cellulose degree of polymerization. For high irradiation doses, there is established a relationship between the absorbed dose and the degree of polymerization. However, a direct relationship between absorbed dose and the parameters of cellulose thermal decomposition for low irradiation doses was not established either in the literature or in our study. By using a peak separation technique, we studied the changes in the region of water loss (70–150 °C) and physical ageing (160–300 °C) for Whatman paper with low initial water content (<1 %), previously gamma irradiated at doses between 0 and 30 kGy. We concluded that strength of the hydrogen bond structure is increasing up to a point when the stress produces fractures in the fibrilar structure. This may explain the results reported for mechanical tests at low dose irradiation and it is in agreement with scanning electron microscopy pictures showing changes in fibril structure at high irradiation doses. Cellulose irradiated at low doses maintains its original hydrogen bond structure despite the decrease of the degree of polymerization.     

Stability of a salicylate-based poly(anhydride-ester) to electron beam and gamma radiation

The effect of electron beam and gamma radiation on the physicochemical properties of a salicylate-based poly(anhydride-ester) was studied by exposing polymers to 0 (control), 25 and 50 kGy. After radiation exposure, salicylic acid release in vitro was monitored to assess any changes in drug release profiles. Molecular weight, glass transition temperature and decomposition temperature were evaluated for polymer chain scission and/or crosslinking as well as changes in thermal properties. Proton nuclear magnetic resonance and infrared spectroscopies were also used to determine polymer degradation and/or chain scission. In vitro cell studies were performed to identify cytocompatibility following radiation exposure. These studies demonstrate that the physicochemical properties of the polymer are not substantially affected by exposure to electron beam and gamma radiation.     

The effect of neutron and mixed gamma and neutron irradiation on the solar properties of borosilicate glass

Neutron and mixed gamma and neutron irradiation, at different absorbed doses, of borosilicate glass with four different chemical compositions was conducted to investigate the effects on the solar properties of the glass. Irradiation was performed in the tangential beam tube and central thimble of a nuclear reactor. The effect of thermal and epithermal neutrons on such solar properties as secondary heat-transfer factor, solar factor (the total solar energy transmittance), and shading coefficient of the borosilicate glass were investigated to determine the effect on the solar properties of borosilicate glass, because of its neutron absorbance property.     

Production of palladium nanoparticles supported on multiwalled carbon nanotubes by gamma irradiation

Palladium nanoparticles were produced and supported on multiwalled carbon nanotubes (MWCNT) by gamma irradiation. A solution with a specific ratio of 2:1 of water-isopropanol was prepared and mixed with palladium chloride and the surfactant sodium dodecyl sulfate (SDS). The gamma radiolysis of water ultimately produces Pd metallic particles that serve as nucleation seeds. Isopropanol is used as an ion scavenger to balance the reaction, and the coalescence of the metal nanoparticles was controlled by the addition of SDS as a stabilizer. The size and distribution of nanoparticles on the carbon nanotubes (CNT) were studied at different surfactant concentrations and radiation doses. SEM, STEM and XPS were used for morphological, chemical and structural characterization of the nanostructure. Nanoparticles obtained for doses between 10 and 40 kGy, ranged in size 5-30 nm. The smaller nanoparticles were obtained at the higher doses and vice versa. Histograms of particle size distributions at different doses are presented.     

Radiation effects on viscosimetry of protein based solutions

Due to their good functional properties allied to their excellent nutritional value, milk protein isolates and soy protein concentrates have gained a crescent interest. These proteins could have their structural properties improved when some treatments are applied, such as gamma irradiation, alone or in presence of other compounds, as a plasticizer. In this work, solutions of those proteins were mixed with a generally recognized as safe plasticizer, glycerol. These mixtures (8% protein (w/v) base) at two ratios 1:1 and 2:1 (protein:glycerol) were submitted to a gamma irradiation treatment (⁶⁰Co), at doses 0, 5, 15 and 25 kGy, and their rheological performance was studied. As irradiation dose increased viscosity measurements decayed significantly (p<0.05) for mixture soy/glycerol and calcium caseinate/glycerol. The mixture sodium caseinate/glycerol showed a trend to form aggregation of macromolecules with dose of 5 kGy, while the apparent viscosity for dispersions containing whey/glycerol remained almost constant as irradiation dose increases. In the case of soy protein isolate and sodium caseinate, a mixture of 2:1 showed a significant higher viscosity (p<0.05) than a mixture of 1:1.