Absorption characterization of Ca2+, Na+, and K+ on irradiation crosslinked carboxymethyl sago pulp hydrogel

Hydrogel of carboxymethyl sago pulp (CMSP) of various degree of substitution (DS) was prepared by electron beam irradiation of various radiation doses. The CMSP hydrogels were subjected to swelling in different ionic strength solutions of KCl, NaCl, and CaCl₂. The CMSP hydrogels, due to its polyelectrolyte nature, were found to be highly sensitive to ionic strength of the medium. All the CMSP hydrogels showed the absorption of K⁺ and Ca²⁺ increases with the increase in the concentrations of the respective cation solutions. The cation absorption also decreases with DS and % gel fraction (%GF) of the CMSP hydrogels. Subjecting the CMSP hydrogels in NaCl results in deswelling and releases Na⁺ to swelling medium where the Na⁺ release increases with the increase of DS and %GF. The sorption capacity depends on the extent of crosslinking and decreases with the increase in the extent of crosslinking. © 2012 Wiley Periodicals, Inc. J. Appl. Polym. Sci., 2013     

Preparation of crosslinked chitosan by electron beam irradiation in the presence of CCl4

In this article, we report the synthesis of crosslinked chitosan using 8 MeV electron beam (EB) irradiation in the presence of carbon tetrachloride. The crosslinked chitosan is characterized by dissolution, Fourier transform infrared spectroscopy (FTIR), X‐ray diffraction (XRD), scanning electron microscopy (SEM), differential scanning colorimetry (DSC), and nanoindentation studies. The insolubility of irradiated films in acetic acid indicates that chitosan has undergone crosslinking reaction. FTIR analysis also confirms the crosslinked structure of chitosan. Mechanical properties such as elastic modulus and hardness are calculated from the nanoindentation data. Modulus and hardness of chitosan increase with increase in the irradiation dose due to the increase in the crosslinking. © 2008 Wiley Periodicals, Inc. J Appl Polym Sci, 2009     

电子束辐照法在水处理中的应用

在介绍电子束辐照机理的基础上，概述了其在环境保护中的应用，并着重从降解有毒有害和难降解的有机污染物、重金属离子的去除等方面对国外就电子束辐照在水处理中的研究和应用现状进行综述，最后对电子束辐照和其他的水处理工艺进行了比较，就其自身可以实现对有毒有害有机物混合液的同时处理、与γ辐射相比具有操作方便、安全的特点，但是自由基与有机物反应的选择性差、易受自由基消耗剂的影响，所需剂量一般较大。并对其在水处理中的应用前景进行了展望。     

Mechanical relaxation of medical grade UHMWPE of different crosslink density as prepared by electron beam irradiation

Dynamic mechanical thermal analysis (DMTA) has been applied on medical grade ultra high molecular weight polyethylene of different crosslink density as prepared by electron beam irradiation to probe for contributions from crosslinking as well as crystallization. The crosslinking proceeds at a crystalline structure with a crystallinity about 50%. With increasing irradiation dose from 0 to 110 kGy, the molar mass between adjacent crosslinks decreases significantly to reach 3170 g/mol at lowest, whereas the crystallite thickness changes and new thin lamellae grow at almost constant degree of crystallinity. From DMTA in the entire temperature range from ?150 to +140°C and the angular frequency range from 0.6 to 135.4 Hz, three relaxation processes γ, β, and α of different temperature position and activation energy are distinguished. The corresponding chain mobility has been discussed as a sensitive discriminator for the coexisting crosslinked and lamellar phases showing the same dimension of a couple of 10 of nanometres. © 2009 Wiley Periodicals, Inc. J Appl Polym Sci, 2009     

Intermolecular crosslinking of poly(acrylic acid) in aqueous solution by electron beam irradiation

Poly(acrylic acid) (PAA) was dissolved in water, and the solution was irradiated with high‐energy electrons. The formation of macroscopic gel was studied as a function of the radiation dose, the pH of the aqueous solution, and the concentration of added salt. Gelation by intermolecular crosslinking was found at low pH values of 2–4, whereas at pH greater or equal to 5, no gel was formed by electron beam irradiation. Nevertheless, by adding monovalent salt the gel formation was enhanced at intermediate pH values. The intermolecular crosslinking was assumed to be inhibited by electrostatic repulsive forces when the macromolecules of PAA are negatively charged and the ionic strength of the solution is low. © 2010 Wiley Periodicals, Inc. J Appl Polym Sci, 2010     

Variation of lexan polycarbonate properties by electron beam

The modifications in microstructural, optical, and photoluminescence properties of the Lexan polycarbonate (bisphenol‐A‐polycarbonate) films exposed to different electron doses have been studied using UV–vis spectroscopy, Fourier transform infrared spectroscopy (FTIR), positron annihilation lifetime spectroscopy, photoluminescence spectroscopy, and scanning electron microscopy (SEM). The obtained UV–vis spectroscopy results showed decrease in optical energy gap, optical activation energy, and increase in number of carbon atoms per cluster with increase in electron dose. The chemical changes in electron irradiated polymers due to chain scission and reconstruction have been observed from FTIR spectroscopy. The correlation of positron lifetime study with optical measurement is obtained, and electron irradiation‐induced microstructural modifications within the polymer is understood. SEM result shows the degradation of Lexan polymer after electron irradiation. The mechanical properties and average molecular weight of Lexan decrease after irradiation, whereas average number of chain scissions per original polymer molecule increases. © 2012 Wiley Periodicals, Inc. J. Appl. Polym. Sci., 2013     

Structure and morphology of isotactic polypropylene functionalized by electron beam irradiation

The structure and morphology of isotactic polypropylene (iPP), functionalized by electron beam irradiation at room temperature in air, are investigated by elementary analysis, FT‐infrared (FTIR) spectroscopy, electron spectroscopy for chemical analysis (ESCA), polariscope, and static contact angle. Elementary analysis reveals that the element oxygen has been introduced onto iPP chains after electron beam irradiation. In addition, as shown from FTIR spectra, oxygen‐containing groups, such as carbonyl, carboxyl, and ether groups, are introduced onto iPP molecular chains. The dependence of oxygenation extent (as measured by O_1S/C_1S value of ESCA spectra) on electron beam dose is obtained. Under polariscope, it can be observed that the dominant alpha phase appears to become more enhanced, and there is no crystalline phase transition. The static contact angle of iPP decreases with increasing dose. © 2000 John Wiley & Sons, Inc. J Appl Polym Sci 76: 75–82, 2000     

Adsorption of methylene blue onto powdered activated carbon immobilized in a carboxymethyl sago pulp hydrogel

The potential of crosslinked carboxymethyl sago pulp (CMSP) beads immobilized with powdered activated carbon (PAC) as an adsorbent for methylene blue (MB) adsorption was investigated. The finely powdered PAC had an excellent adsorption capacity for MB but was disadvantageous for the separation process from treated effluents. To ease the separation process, the CMSP medium could be advantageous for the process by acting an immobilizing medium for PAC. The MB adsorption reached equilibrium at the 14th hour, and further adsorption was studied to determine the effects of the CMSP concentration, PAC dosage, and pH. Different CMSP concentrations in the preparation of CMSP–PAC beads showed no significant differences; this proved that CMSP–PAC adsorbed more MB than CMSP did. The MB adsorption increased with increasing PAC concentration, whereas the CMSP–PAC beads disintegrated at pH 11.5. In the equilibrium study, the Langmuir isotherm fit well into the experimental data with a linear correlation coefficient (R ²) of 0.9837 and a maximum adsorption capacity of 250 mg/g. The kinetic study showed that pseudo‐second‐order kinetics accommodated the experimental data well with an R ² value of 0.9512 and a pseudo‐second‐order rate constant value of 3.61 × 10^?3 min^?1. The crosslinked CMSP–PAC beads have the potential to remove MB dye, and this could be exploited as an alternative to treating colored dye effluents produced by industries such as the textile, printing, and cosmetics industries. © 2016 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2017 , 134 , 44271.     

Crosslinking of cis-1,4-polyisoprene rubber by electron beam irradiation

Various unsaturated polyfunctional monomers were kneaded into cis-1,4-polyisoprene containing fillers under 80°C and then irradiated using an electron beam accelerator to prepare vulcanized rubber with good quality. Results showed that 2G (diethyleneglycol dimethacrylate) is the best sensitizer. The optimal tensile strength of vulcanized IR was obtained by using 14 phr 2G and irradiated to 180 kGy. Compared with the sulfur vulcanizate, greater values of tensile strength, elongation at break, and 100% stress were found with the radiation-cured IR. Their Young's modulus and tan σ were similar. © 1997 John Wiley & Sons, Inc. J Appl Polym Sci 66: 113–116, 1997     

微波辐照合成聚丙烯酸水凝胶及其性能研究

采用微波辐照法合成了聚丙烯酸水凝胶,并对其溶胀性能进行了研究。所制得的凝胶不仅具有pH敏感性和良好的pH反复性,而且在pH<4的酸性溶液中表现出温度敏感性,其溶胀比随温度的升高而上升。     

Electron beam irradiation of polytetrafluoroethylene in vacuum at elevated temperature: An infrared spectroscopic study

Electron beam irradiation of polytetrafluoroethylene (PTFE) has been performed in vacuum both at elevated temperature above the melting point of PTFE and at room temperature for comparison. The changes in the chemical structure were studied by Fourier‐transform infrared (FTIR) spectroscopy. The formation of double bonds in PTFE was confirmed as a result of irradiation in vacuum. Moreover, trifluoromethyl (CF₃) branches were detected. The concentration of CF₃ branches was found to be much higher in irradiation at elevated temperature than in room temperature irradiation. The CF₃ branches are assumed to cause the reduced crystallinity indicated by the transparency of PTFE specimens irradiated in the molten state. © 1999 John Wiley & Sons, Inc. J Appl Polym Sci 74: 1571–1576, 1999     

Synthesis of starch‐based plastic films by electron beam irradiation

Starch‐based plastic films were prepared by the electron beam irradiation of starch and poly(vinyl alcohol) (PVA) in a physical gel state at room temperature. The influence of starch/PVA composition, irradiation dose, and plasticizer (glycerol) on the properties of the plastic films was investigated. The gel fraction of the starch/PVA films increased with both the radiation dose and PVA content in the plastic film and decreased with increasing glycerol concentration. The starch/PVA compatibility was determined by measurement of the thermal properties of the starch/PVA blends with various compositions with differential scanning calorimetry. The swelling of the starch/PVA films increased with increasing PVA content and decreasing irradiation dose. Mechanical studies were carried out, and the tensile strength of the films decreased at high starch ratios in the starch‐based mixture. This was due to the decrease in the degree of crosslinking of starch. Furthermore, when PVA, a biodegradable and flexible‐chain polymer, was incorporated into the starch‐based films, the properties of the films, such as the flexibility (elongation at break), were obviously improved. The tensile strength of the films decreased with increasing glycerol concentration, but elongation at break increased up to a maximum value at a 20% glycerol concentration, and then, it leveled off and decreased slightly. Biodegradation of the starch/PVA plastic films was indicated by weight loss (%) after burial in soil and morphological shape, which was detected by scanning electron microscopy. © 2007 Wiley Periodicals, Inc. J Appl Polym Sci 104: 504–513, 2007     

Influence of electron beam sterilization on polymers when incubated in different media

Polyurethane catheters were irradiated with electron‐beam. We looked at the way the catheter is physically and chemically modified after incubation in different media. An extracting medium (methanol) was compared to other oxidative, enzymatic, and saline aqueous media, mimicking some aspects of biological fluids. Irradiation had a strong impact on the stability of polymer during incubation. For nonirradiated samples incubated in aqueous media, only a small diffusion of additives was observed; no oligomer release was put into evidence, and the polymer was almost not degraded. But the chain branching that occurred because of irradiation created some weaknesses in the polymer chains: irradiated samples were mostly sensitive to chain scission and oligomers released during incubation; this trend increased with the irradiation dose. © 2008 Wiley Periodicals, Inc. J Appl Polym Sci, 2009     

Dynamic mechanical analysis of polyethylene and ethylene vinylacetate copolymer blends irradiated by electron beam

Dynamic mechanical properties of nonirradiated and irradiated blends of polyethylene (PE) and ethylene vinylacetate (EVA) copolymer have been determined. Effect of addition of EVA and radiational crosslinking on loss and storage modulus, tan δ, and transition temperatures were determined. Increase in transition temperatures on exposure to radiation and decrease in transition temperatures with addition of EVA is observed. Peak broadening is observed on exposure to radiation. Values of the storage modulus increase while that of loss modulus and tan δ decrease on crosslinking. © 2002 Wiley Periodicals, Inc. J Appl Polym Sci 86: 2429–2434, 2002     

Effect of electron beam irradiation on polyacrylonitrile precursor fibers and stabilization process

The electron beam was imposed on the polyacrylonitrile precursor fibers before the fibers were stabilized. The effect of electron beam irradiation on the chemical structure, transverse section, and surface morphology and thermal properties of the fibers in the process of stabilization was characterized by the use of Fourier transform infrared spectroscopy (FTIR), scanning electron microscope (SEM), and differential scanning calorimeter, respectively. A parameter η = I(C?N)/[I(C?N) + I(C?N)] was defined to evaluate the extent of cyclization in the stabilization process. The kinetic parameters, viz. activation energy (E) and pre‐exponential factor (A) of the stabilization reactions, were calculated by Kissinger method. FTIR analysis indicated that the cyclization of nitrile groups was initiated at room temperature by electron beam irradiation. The transformation of C?N groups to C?N ones was accelerated in the process of stabilization. The extent of cyclization of the stabilized fibers was increased. SEM analysis indicated that irradiation could also decrease the internal and surface defects of the stabilized fibers treated at 300°C. The activation energy of cyclization reaction was reduced from 302 to 280 kJ/mol and 260 kJ/mol through 100 and 200 kGy electron beam irradiation, respectively. The reaction temperature range was expanded, and the exothermic rate was slowed down in the process of stabilization, which was the reason why the stabilized fibers have improved cyclization degree and less internal defects. © 2011 Wiley Periodicals, Inc. J Appl Polym Sci, 2011     

Effects of γ‐aminopropyltriethoxylsilane on morphological characteristics of hybrid nylon‐66‐based membranes before electron beam irradiation

Nylon‐66 is a typical semicrystalline polymer that can be crosslinked using crosslinking agents and electron beam irradiation. Hybrid nylon‐66‐based membranes are more porous but denser compared to the pure nylon‐66 membrane. Besides that, hybrid nylon‐66 membranes exhibit higher water uptake and severe swelling in water. Si/nylon‐66 membranes were prepared by adding γ‐aminopropyltriethoxylsilane (APTEOS). Crosslinked silica in nylon‐66 membranes is confirmed with high gel content and Fourier transform infrared peaks, but XRD results showed that there is a low crystalline degree in these membranes. The thermal stability of hybrid nylon‐66 membranes is also less affected by APTEOS. The crosslinking agent only improves storage modulus in hybrid nylon‐66 membranes. After irradiation, it is learned that APTEOS improves separation performance of nylon‐66 membranes. However, excessive APTEOS causes the ratio of effective thickness over porosity (Δx/A_k) reduces significantly resulting a lower permeability membrane. © 2011 Wiley Periodicals, Inc. J Appl Polym Sci, 2011     

电子束辐射接枝对PAN基碳纤维的表面改性

采用电子束加速器辐射接枝方法对聚丙烯腈(PAN)基碳纤维进行表面改性,研究了接枝单体种类对接枝率及其环氧树脂基复合材料力学性能的影响,分析了辐射接枝前后PAN基碳纤维的表面形貌与化学结构以及其复合材料界面断口的形貌变化。结果表明:电子束辐射接枝改性的PAN基碳纤维表面粗糙度增加,表面活性官能团增多,与树脂的机械锲合作用增强,其树脂基复合材料断口表而较为平整;乙二胺/水溶液体系是辐射接枝改性的理想溶液,在200 kGy的电子束辐射下,PAN基碳纤维表面的接枝率为6.66%,复合材料的层间剪切强度提高了45.1%。     

Degradation of poly(D,L‐lactic acid)‐b‐poly(ethylene glycol) copolymer and poly(L‐lactic acid) by electron beam irradiation

This article investigated the effects of electron beam (EB) irradiation on poly(D ,L ‐lactic acid)‐b‐poly(ethylene glycol) copolymer (PLEG) and poly(L ‐lactic acid) (PLLA). The dominant effect of EB irradiation on both PLEG and PLLA was chain scission. With increasing dose, recombination reactions or partial crosslinking of PLEG can occur in addition to chain scission, but there was no obvious crosslinking for PLLA at doses below 200 kGy. The chain scission degree of irradiated PLEG and PLLA was calculated to be 0.213 and 0.403, respectively. The linear relationships were also established between the decrease in molecular weight with increasing dose. Elongation at break of the irradiated PLEG and PLLA decreased significantly, whereas the tensile strength and glass transition temperature of PLLA decreased much more significantly compared with PLEG. The presence of poly(ethylene glycol) (PEG) chain segment in PLEG was the key factor in its greater stability to EB irradiation compared with PLLA. © 2010 Wiley Periodicals, Inc. J Appl Polym Sci, 2011     

Modification of nylon 66 by electron beam irradiation for improved properties and superior performances

Nylon 66 has been transformed into a material with significantly improved properties like hardness, tensile strength, and flexural modulus by processing it under the optimized dose rate of electron beam in the presence of suitable crosslinkers. Furthermore, percent water absorption of nylon 66 was reduced substantially on irradiation. Thermogravimetric analysis revealed that thermal stability of nylon 66 improved with increasing dose of radiation. Improvement of mechanical and thermal properties and reduction of water absorption of nylon 66 were due to the crosslinking of polyamide molecules made possible by the high energy radiation. Increase of crosslinking with increasing radiation dose was verified by the increase of gel content at higher doses. Differential scanning calorimetry showed that both melting and crystallization temperatures along with percent crystallinity of nylon 66 were decreased with the increasing dose of radiation leading to the development of more amorphous character in this semicrystalline polymer. © 2011 Wiley Periodicals, Inc. J Appl Polym Sci, 2011.     

PAA/PNIPAAm互穿网络水凝胶的微波合成与性能研究

以微波为辐射源,对丙烯酸(AA)水溶液进行辐照制得了PAA水凝胶。将脱水后的PAA水凝胶浸泡于含引发剂过硫酸钾(K_2S_2O_8)和交联剂N,N’-亚甲基双丙烯酰胺(BIS)的N-异丙基丙烯酰胺(NIPAAm)水溶液中,待溶胀平衡后取出,进行第二次微波辐照反应,制备了聚丙烯酸/聚N-异丙基丙烯酰胺互穿聚合物网络(PAA/PNIPAAm IPN)水凝胶,并对其溶胀性能进行了研究。研究结果表明,合成的IPN水凝胶兼具pH敏感性和温度敏感性,有望在药物控制释放领域得到应用。