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1.
The radiolytic stability of a promising extractant for actinide partitioning from high-level radioactive liquid waste, namely N,N,N',N'-tetraoctyl diglycolamide (TODGA) was investigated in the presence of several phase modifiers, viz. N,N-dihexyloctanamide (DHOA), tri-n-butyl phosphate (TBP), 1-decanol, and iso-decanol dissolved in n-dodecane. The distribution ratio of Am(III) decreased with increased radiation dose studied up to 1000 kGy. Nevertheless, all the compositions of extractants showed fairly high extraction of Am(III) up to 500 kGy (DAm: ≥ 50), beyond which significant decrease was observed. However, the DAm values were sufficiently high for process applications for the chosen compositions even at an absorbed dose of 1000 kGy. The stripping behavior of Am(III) with 0.2 M HNO3 was found to be favorable with increased absorbed dose by the solvent up to 1000 kGy. With an increased absorbed dose, the loading of Nd(III) in the organic phase decreased due to depletion of ligand/extractant concentration (TODGA) in the organic phase. There was marginal variation in the hydrodynamic parameters such as density, viscosity, and interfacial tension (IFT) of the irradiated solvents vis-a-vis fresh/unirradiated solvent.  相似文献   

2.
The mechanical properties of poly(ethylene terephthalate)/high-density poly(ethylene) (PET/HDPE) blends were improved by γ-ray irradiation combined with using a cross-linking agent—trimethylol propane trimethacrylate (TMPTA). The effect of the weight ratio of PET/HDPE, the content of TMPTA and the absorbed dose on the phase morphology and the mechanical properties of the PET/HDPE blends were investigated through scanning electron microscopy (SEM), gel fraction, Fourier transform infrared spectroscopy (FTIR), tensile and impact tests. SEM images showed that the phase structure changed significantly as TMPTA coexistence. The results of tensile and impact tests indicated that their mechanical properties depended on their structures. FTIR spectra suggested that a new structure of HDPE-g-PET was generated. When the weight ratio of PET/HDPE blend was 80/20, the content of TMPTA was 1 wt% and the absorbed dose was 30 kGy, the tensile strength, elongation at break and impact strength of irradiated blends were improved greatly compared with non-irradiated blends.  相似文献   

3.
Isotactic polypropylene (PP) was preradiated by γ ray with different absorbed doses and subsequently blended with ethylene‐vinyl acetate (EVA) co‐polymer to prepare PP/EVA blends. The average molecular weight (Mn) of isotactic PP decreased with the increasing radiation absorbed dose, which indicated that high energy radiation of γ ray broke the isotactic long PP chains into shorter ones. The melt flow rate results evidenced that the processing ability of PP/EVA blends was continuously promoted with the increasing absorbed dose. The β crystal was obtained in the PP/EVA blends by the radiation method. The onset temperatures and peaks of crystallization of PP/EVA blends decreased slightly with the increasing radiation absorbed dose, while high energy radiation was inclined to enhance the crystallinity of PP/EVA blends. The Fourier transform infrared spectroscopy (FTIR) tests confirmed an interesting phenomenon that PP tended to move to the surface of the PP/EVA blends with the increasing radiation absorbed dose. Mechanical tests proved that the PP/EVA blends remained a comparative stable mechanical property under the absorbed dose of 30 kGy. The experimental results indicated that PP/EVA blend was a potential candidate for industrial applying. © 2017 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2017 , 134, 45057.  相似文献   

4.
《分离科学与技术》2012,47(5):646-653
The organic solvent phase composed of N,N,N’,N’-tetra-2-ethylhexyl diglycolamide (TEHDGA) and bis(2-ethylhexyl)phosphoric acid (HDEHP) in n-dodecane (n-DD) is regarded as a promising candidate for single-cycle separation of americium (III) from high-level liquid waste. The radiochemical degradation of a solution of TEHDGA + HDEHP/n-DD was investigated by irradiating the solvent to various absorbed dose levels of γ-radiation. The neat extractants or a solution of extractants in n-dodecane were irradiated in the presence and absence of nitric acid. The degree of degradation was assessed by measuring the variation in the extraction behavior of Am(III), Eu(III) and other metal ions in irradiated solvent systems. The distribution ratio of americium and europium decreased with increase of absorbed dose. The presence of n-dodecane enhanced the radiolytic degradation of the solvent; however, the role of nitric acid during degradation was insignificant. The recovery of Am(III) and Eu(III) from the irradiated solvent system was studied. The recovery of Am(III) was quantitative in 3 contacts; however, the separation factor of Eu(III) over Am(III) during stripping decreased marginally with increase of absorbed dose.  相似文献   

5.
Blends of poly(ethylene terephthalate) (PET) and poly(ethylene octene) (POE) were prepared by melt blending with various amounts of trimethylolpropane triacylate (TMPTA). The mechanical properties, phase morphologies, and gel fractions at various absorbed doses of γ‐irradiation have been investigated. It was found that the toughness of blends was enhanced effectively after irradiation as well as the tensile properties. The elongation at break for all studied PET/POE blends (POE being up to 15 wt %) with 2 wt % TMPTA reached 250–400% at most absorbed doses of γ‐irradiation, approximately 50–80 times of those of untreated PET/POE blends. The impact strength of PET/POE (85/15 wt/wt) blends with 2 wt % TMPTA irradiated with as little as 30 kGy absorbed dose exceeded 17 kJ/m2, being approximately 3.4 times of those of untreated blends. The improvement of the mechanical properties was supported by the morphology changes. Scanning electron microscope images of fracture surfaces showed a smaller dispersed phase and more indistinct inter‐phase boundaries in the irradiated blends. This indicates increased compatibility of PET and POE in the PET/POE blends. The changes of the morphologies and the enhancement of the mechanical properties were ascribed to the enhanced inter‐phase boundaries by the formation of complex graft structures confirmed by the results of the gelation extraction and Fourier Transform Infrared analyses. © 2012 Wiley Periodicals, Inc. J. Appl. Polym. Sci., 2013  相似文献   

6.
赵雪娜 《橡胶工业》2018,65(12):1398-1401
本文对氢化丁腈(HNBR)硫化胶进行γ射线的辐照处理,研究不同吸收剂量对HNBR硫化胶物理机械性能、压缩永久变形和回弹性等性能的影响。从HNBR的结构来推理,属于辐照交联型聚合物,我们的实验结果也从宏观上验证了这一结论。随着吸收剂量的增加,其硫化胶的拉伸强度先上升后下降,在200kGy时达到最大值;硫化胶的扯断伸长率随着吸收剂量的增加呈现下降趋势;随着吸收剂量的增大,硫化胶的回弹性呈增大趋势,压缩永久变形呈下降的趋势。  相似文献   

7.
考察了敏化剂和聚合物改性添加剂对聚乙烯的辐射交联效应。测定了敏化剂及添加剂用量,吸收剂量对交联聚乙烯各项性能的影响。结果表明,敏化剂及添加剂的加入能在较低吸收剂量下有效地提高PE的凝胶分数,改善其机械性能,提高了热性能。  相似文献   

8.
Crosslinking of ultra high molecular weight polyethylene fibers (UHMW‐PE fibers) is investigated by means of electron beam irradiation. The structure and mechanical properties of the fibers in different irradiation atmospheres are discussed. The results show that the gel fraction and crosslinking density increase with the increase of absorbed dose. The swelling ratio and average molecular weight of crosslinked net decrease with the increase of absorbed dose. The relation between s + s?1 of the UHMW‐PE fibers and reciprocal irradiation dose 1/R is obtained. The tensile strength and failure elongation decrease with the increase of absorbed dose, and the tensile modulus increases with the increase of absorbed dose. The samples are irradiated in air, vacuum, and acetylene atmospheres, separately. The radiation effects, such as crosslinking fraction and mechanical properties of UHMW‐PE fibers, are the most significant in acetylene atmosphere in comparison with in air and in vacuum. © 2005 Wiley Periodicals, Inc. J Appl Polym Sci 98: 1761–1764, 2005  相似文献   

9.
Abstract

Cobalt dicarbollide and polyethylene glycol in phenyltrifluoromethyl sulfone (HCCD/PEG in FS‐13) is currently under consideration for use in the process‐scale selective extraction of fission product cesium and strontium from acidic radioactive solutions. While the Cs and Sr solvent extraction efficiency of this formulation has been previously characterized, this solvent will be exposed to high radiation doses during use, and has not been adequately investigated for radiation stability. Here, HCCD/PEG was γ‐irradiated to various absorbed doses, to a maximum of 432 kGy, using 60Co. Irradiations were performed for the neat organic phase, and also for the organic phase in contact with 1 M‐nitric acid mixed by air sparging. Post‐irradiation solvent extraction measurements showed that Cs distribution ratios were unaffected; however, strontium distribution ratios decreased with the absorbed dose under both conditions. The decrease in the extraction efficiency for strontium was greater when in contact with the aqueous phase. The stripping performance was not affected. A mechanism, based on reaction with the products of direct diluent radiolysis, is proposed to explain the decreases in the strontium extraction efficiency.  相似文献   

10.
The physicochemical changes of silk fibers irradiated with γ-rays was studied in relation to the amount of absorbed does in the range 0–21 Mrad. The yellowing index (b/L) suddenly increased at low dose for both raw and degummed silk fibers. An equilibrium value was attained from 10 Mrad upward. The tensile properties were significantly affected by exposure to γ-rays. Both strength and elongation at break decreased at almost the same rate and extent, attaining a final value that was one-half of the untreated control. The birefringence and isotropic refractive index of exposed silk fibers decreased, the effect being larger in the low dose range, suggesting a decrease of crystallinity and molecular orientation. X-ray diffraction curves, however, demonstrated that the crystalline structure remained unchanged even after exposure of the highest γ-ray dose. The thermal behavior evaluated by DSC and TMA measurements showed that the γ-irradiation induced a slight decrease of thermal stability in irradiated silk fibers, this effect being detectable only at 21 Mrad of the absorbed dose. The dynamic viscoelastic behavior suggested that the thermal movement of the fibroin molecules in the amorphous and crystalline regions increased with increasing absorbed dose, attributing to the physicochemical modifications induced by the ionizing radiations. © 1994 John Wiley & Sons, Inc.  相似文献   

11.
This study reports the influences of gamma irradiation (GI) in the range of 20–100 kGy on CuO thin films via thermal spray pyrolysis technique on the glass substrates. The results demonstrate significant influences of GI on the crystallographic, microstructural and optical characteristics of CuO thin films. The obtained XRD results showed that the crystallinity of the films deteriorates by gradually decreasing crystallite size (from 59.13 to 46 nm) as applied gamma doses increases. However, the basic monoclinic crystal structure remains same. The dislocation density and lattice strain increased with the rise of GI absorbed dose due to the creation of defects. The values of number of crystallites per unit surface area increased as dose increased indicating the abundance of crystallization of nano CuO thin films. A UV–Vis–NIR spectrophotometer was utilized to determine the optical properties and obtained results indicated that the optical energy band gap (OBG) energies reduced from 2.00 to 1.72 eV as the doses increased from 0 to 100 kGy. No distinctions of the monoclinic phase of virgin CuO thin film have been perceived under applied absorbed doses, notwithstanding the slight deterioration of the crystallinity and narrowing the OBG.  相似文献   

12.
Abstract

N,N,N′,N′-tetra(2-ethylhexyl)diglycolamide (TEHDGA) was found to be a promising extractant for actinide partitioning from high-level waste (HLW) (Part I). In order to evaluate the applicability of TEHDGA to the HLW partitioning process, investigations on its radiolytic stability were carried out. The present work deals with the studies on the uptake of americium by γ-irradiated 0.2 M TEHDGA/n-dodecane in the absence and presence of phase modifiers—di(n-hexyl)octanamide (DHOA), isodecanol and n-decanol—against the absorbed dose up to 1 × 106 Gy in the presence of nitric acid at varying concentrations. The addition of phase modifiers suppressed the radiolysis of TEHDGA in n-dodecane and DHOA was found to be the most effective radiolysis suppressor. Investigations were also carried out on the degradation of neat TEHDGA by γ-irradiation, and it was attempted to isolate and identify its degradation products by instrumental analysis. The radiolysis study showed that the degradation products were formed by the cleavage of the –C-N bond, to eliminate an ethylhexyl group, and the bond adjacent to the ether bond. The results obtained for TEHDGA radiolysis were compared with that of its straight-chain isomer TODGA, and TEHDGA was observed to be more resistant to radiation than TODGA. The changes in the physico-chemical properties of γ-irradiated TEHDGA against the absorbed dose were also investigated.  相似文献   

13.
Two schemes, the first involving ozonation followed by final aerobic biodegradation (phase I experiments), and the second involving initial aerobic biodegradation, followed by ozonation and subsequent final aerobic biodegradation (phase II experiments), were examined for enhanced mineralization of refractory model compounds, viz. gallic acid, tannin and lignin. In all cases, and irrespective of the applied scheme, chemical oxygen demand (COD), total organic carbon (TOC), COD/TOC ratio, and specific UV absorbance at 280 nm attributed to the model compounds decreased with application of increasing ozone dose. The residual organic matter remaining after ozonation exhibited enhanced aerobic biodegradability in all cases. Further, in all cases and irrespective of the applied scheme, the overall amount of COD and TOC removed through the combination of ozonation and biodegradation processes increased with increase in ozone dose for all three model compounds, and more than 90% COD removal could be achieved with an ozone dose of 3 mg ozone absorbed per mg initial TOC, as compared with approximately 40% COD removal when no ozone was applied. Treatment by the first scheme resulted in the fraction of starting COD removed through biodegradation decreasing with increase in ozone dose in all cases, while this fraction increased or remained constant during treatment using the second scheme. In the case of tannin and lignin, similar overall COD removal could be achieved at lower ozone doses using scheme II. Due to incorporation of the initial aerobic biodegradation step in scheme II, the ozone requirement for additional mineralization, ie mineralization over and above that achieved by aerobic biodegradation, was also lower than that in scheme I. Copyright © 2005 Society of Chemical Industry  相似文献   

14.
Crosslinking of homemade low‐density polyethylene (LDPE) was performed by electron‐beam (EB) irradiation. The gel content of the EB‐exposed LDPE was determined by the solvent‐extraction method. The degree of crosslinking was also evaluated by a hot set measuring test. The results obtained from both the gel–sol and the hot set methods showed that the degree of crosslinking was dependent on the deposited energy in LDPE samples. Increasing the absorbed dose increased the degree of network formation. The LDPE with higher molecular weight yielded higher efficiency of crosslinking at the same irradiation dose. The effect of irradiation dose on the molecular weight between crosslinks (Mc), glass‐transition temperature, and free volume were calculated. Mechanical test results showed that the tensile strength of the samples increased with increase in the irradiation dose up to 150 kGy and then slightly decreased with further increasing the deposited energy. The elongation at break decreased with increasing the absorbed dose. The results obtained from differential scanning calorimetry exhibited a small reduction in the melting point and the degree of crystallinity of the EB‐exposed LDPE samples compared to those of the untreated samples. The effect of crosslinking on the electrical properties of the irradiated samples was insignificant. The dielectric constant of the treated samples remained nearly constant within the irradiation dose range, although the dissipation factor increased slightly with increasing the absorbed dose. The results obtained from characterizing the EB‐induced crosslinking of homemade polyethylene, including LH0030 and LH0075, showed the higher molecular weight polyethylene (LH0030) as a preferred option for wire and cable insulation. © 2002 Wiley Periodicals, Inc. J Appl Polym Sci 86: 1959–1969, 2002  相似文献   

15.
High energy electrons have been used to induce chemical crosslinking in 50/50 blend of polypropylene and natural rubber. The blend morphology was generated during melt mixing and not changed by high energy electron treatment in the solid state at room temperature. The variation of absorbed dose (150–350 kGy) at fixed electron energy (1.5 MeV) brings a dramatic change in the properties of the polymer blend. In addition, the effect of a polyfunctional monomer (PFM) and the absorbed dose on the tensile properties of the polymer blend was investigated. The presence of a PFM led to blends having an elongation at break of about 350% and a tensile strength of nearly 14 MPa after the treatment with a comparatively low dose of 150 kGy. The morphology of the blends was found to be co‐continuous. A plausible mechanistic pathway for the phenomenon leading to enhancement of property has been suggested for better understanding of structure–property‐relationship. POLYM. ENG. SCI., 2013. © 2012 Society of Plastics Engineers.  相似文献   

16.
采用电子束高温辐照制备交联聚四氟乙烯(XPTFE),利用环-环立式万能摩擦磨损试验机在干摩擦条件下研究了PTFE和XPTFE的摩擦磨损性能变化规律。结果表明:与PTFE的摩擦系数相比,XPTFE的摩擦系数随剂量的增加而增加。随剂量的增加,XPTFE的耐磨性增大,当吸收剂量为150 kGy时,XPTFE耐磨性提高了近1 000倍。PTFE磨损表面光滑,磨屑为波浪形带状物;XPTFE的磨损表面形成摩擦棱,磨屑为粉状颗粒。XPTFE的三维网状交联结构导致其耐磨性能明显提高。  相似文献   

17.
Natural rubber latex and various concentration of natural antioxidant were blended in different ratios and irradiated at various absorbed doses by gamma rays from Co-60 source at room temperature. The aqueous extraction of Diospyros peregrina was used as natural antioxidant. It was found that the addition of different concentration of natural antioxidant into natural rubber latex improve the aging property of the film. Decreasing in tensile strength of rubber film with 10 phr natural antioxidant and 15 kGy radiation dose after 24 hours aging at 100°C was 9.34% compared to 13.89% for film without natural antioxidant. The tensile strength, tear resistance and modulus at 500% elongation of the rubber film were found to be optimum at 15 kGy radiation dose and with 10 phr natural antioxidant. Elongation at break, permanent set and swelling ratio decreases with the increasing absorbed radiation dose as well as the concentration of the natural antioxidant.  相似文献   

18.
Gamma radiation has been used to initiate the gas phase reaction between iodine and methane. Under appropriate conditions, the products are hydrogen iodide and the iodomethanes. The experiments were conducted over a range of temperature, concentration, and at two levels of total absorbed dose. The existence of a chain reaction is presumed, on the basis of G-values, which were as high as 7 × 107. In view of the propensity of iodine as a radical scavenger, this high efficiency might seem surprising, but may be attributable to the known autocatalyic effect of iodine in substitution reactions.  相似文献   

19.
A new chemically oriented mathematical model for the development step of the LIGA process is presented (LIGA is an acronym for the German words Lithographie, Galvanoformung, and Abformung). The key assumption is that the developer can react with the polymeric resist material to increase the solubility of the latter, thereby partially overcoming the need to reduce the polymer size. The ease with which this reaction takes place is assumed to be determined by the number of side‐chain scissions that occur during the X‐ray exposure phase of the process. The dynamics of the dissolution process are simulated by the solution of the reaction diffusion equations for this three‐component, two‐phase system, the three species being the unreacted and reacted polymers and the solvent. The mass fluxes are described by multicomponent diffusion (Stefan–Maxwell) equations, and the chemical potentials are assumed to be given by the Flory–Huggins theory. Sample calculations are used to determine the dependence of the dissolution rate on key system parameters such as the reaction rate constant, polymer size, solid‐phase diffusivity, and Flory–Huggins interaction parameters. A simple photochemistry model is used to relate the reaction rate constant and the polymer size to the absorbed X‐ray dose. The resulting formula for the dissolution rate as a function of the dose and temperature is fit to an extensive experimental database to evaluate a set of unknown global parameters. The results suggest that reaction‐assisted dissolution is very important at low doses and low temperatures, the solubility of the unreacted polymer being too small for it to be dissolved at an appreciable rate. However, at high doses or at higher temperatures, the solubility is such that the reaction is no longer needed, and dissolution can take place via the conventional route. These results provide an explanation for the observed dependences of both the rate of dissolution and its activation energy on the absorbed dose. © 2005 Wiley Periodicals, Inc. J Appl Polym Sci 97: 25–37, 2005  相似文献   

20.
ABSTRACT

Dicyclohexano- 18-crown-6 (DC18C6), dissolved in chloroform, 1-octanol, toluene or cyclohexane, was irradiated by 60Co γ-rays. Radiolytic destruction of DC18C6, measured by gas chromatography, decreased in the order: chloroform > cyclohexane > 1-octanol > toluene. Distribution coefficients in the solvent extraction of strontium from nitric acid solution were measured. These distribution coefficients were minimally affected by γ-irradiation in toluene solution, but decreased with the absorbed dose in chloroform solution. It was suggested that the distribution coefficient for the liquid-liquid extraction system was influenced by radiolytic products. The effect of radiolytic products on the distribution coefficients was evaluated by considering DC18C6 remaining in the organic phase after irradiation. The distribution coefficient measured for the organic phase with radiolytic products was larger than that without radiolytic products. The radiolytic products were thus shown to contribute to the increase in the distribution coefficient.  相似文献   

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