Cationic polymerization behavior of β‐methylglycidyl ether derivatives and physical properties of their cationically cured materials

β‐Methylglycidyl ethers have been applied to Electrical and Electronic adhesives. However, there is no report about the detailed polymerization behavior and physical properties of their cured products. Hence, we investigated cationic polymerization behavior of bisphenol A di(β‐methylglycidyl) ether (Me‐BADGE) and physical properties of the cured products containing Me‐BADGE. DSC analysis suggested that Me‐BADGE could be cured completely at lower temperature than bisphenol A diglycidyl ether (BADGE). Physical properties were analyzed by dynamic viscoelastic analysis. Glass transition temperature (T_g) of BADGE homopolymer was 194°C. In contrast, the copolymer of BADGE (50 wt %) with Me‐BADGE (50 wt %) showed T_g at 124°C. According to the data of E’ and tan δ, crosslink density of the cured products decreased with increasing the Me‐BADGE content. The analysis of cationic polymerization of monofunctional β‐methylglycidyl ether suggested that the cationic polymerization proceeded not only through oxonium cation but also through carbocation formed by ring‐opening reaction of oxonium cation. © 2015 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2015 , 132, 42377.     

Functional binders for reversible lithium intercalation into graphite in propylene carbonate and ionic liquid media

Poly(acrylic acid) (PAA), poly(methacrylic acid) (PMA), and poly(vinyl alcohol) (PVA), which have oxygen species as functional groups, were utilized as a binder for graphite electrodes, and the electrochemical reversibility of lithium intercalation was examined in PC medium and ionic liquid electrolyte, lithium bis(trifluoromethanesulfonyl)amide dissolved in 1-butyl-1-methylpyrrolidinium bis(trifluoromethanesulfonyl)amide (BMP-TFSA). Columbic efficiency of 75–80% with more than 300 mAh g^?1 was achieved upon first reduction/oxidation cycle in both electrolytes using these binding polymers, which were significantly improved in comparison to a conventional PVdF binder (less than 45% of columbic efficiency for the first cycle). For the graphite-PVdF electrode, co-intercalation and/or decomposition of PC molecules solvating to Li ions were observed by the electrochemical reduction, resulting in the cracking of graphite particles. In contrast, the co-intercalation and decomposition of PC molecules and BMP cations for the first reduction process were completely suppressed for the graphite electrodes prepared with the polymers containing oxygen atoms. It was proposed that the selective permeability of lithium ions was attained by the uniform coating of the graphite particles with PAA, PMA, and PVA polymers, because the electrostatic interaction between the positively charged lithium ions and negatively charged oxygen atom in the polymer should modulate the desolvation process of lithium ions during the lithium intercalation into graphite, showing the similar functions like artificial solid-electrolyte interphase.     

Influence of phosphate species on green rust I transformation and local structure and morphology of γ-FeOOH

To clarify the role of phosphate in the formation of corrosion products, the transformation of GRI(Cl⁻) with the addition of phosphate was characterized through XRD, TEM, and solution analysis. Electrochemical analysis showed that the transformation of GRI(Cl⁻) was delayed and the size of the final products, i.e., γ-FeOOH was reduced in the phosphate added case. X-ray absorption spectroscopy indicated that the neighboring Fe–Fe coordination number of FeO₆ octahedral unit in γ-FeOOH was decreased. These effects of phosphate are attributed to its adsorption on GRI(Cl⁻) and nucleated γ-FeOOH that prevented particle growth during oxidation process.     

Improvement of sensing characteristics of self‐sensing active magnetic bearings

A winding‐current interference model of self‐sensing magnetic bearings (AMBs) and an improvement technique of position‐sensing characteristics are proposed. In the self‐sensing AMB systems, the electromagnets work not only as actuators suspending the rotor but also as position sensors. The self‐sensing position signal, however, includes errors because of nonlinearity of the magnetic circuits. In the proposed model, the current is directly transmitted to the self‐sensing position signal. This transmission means degradation of the self‐sensing characteristics. This winding‐current interference to the self‐sensing signal is reduced by the proposed compensation method. The characteristics of the proposed self‐sensing method agree well with a reference sensor signal up to over 1 kHz. © 2008 Wiley Periodicals, Inc. Electr Eng Jpn, 166(2): 70– 77, 2009; Published online in Wiley InterScience ( www.interscience.wiley.com ). DOI 10.1002/eej.20732 Copyright © 2004 Wiley Periodicals, Inc.     

Fabrication of aluminium foams from powder by hot extrusion and foaming

In order to produce aluminium foams for light-weight and energy absorbing structures of automobiles, a method for fabricating aluminium foam from powder mixed with a foaming agent by using a mould is proposed. The method consists of four sequential processes: powder compacting, extruding, foaming and moulding. In the experiment for fabricating aluminium foam from powder, the conditions of powder extrusion and foaming by the heated die are determined from the density of the aluminium foams made without a mould. The experimental results show that the relative density of the aluminium foam made under appropriate conditions is 0.22. In moulding of aluminium foam, a stainless steel pipe is used as a mould and the cylindrical aluminium foam is produced by filling into the pipe mould. The distribution of relative density within the aluminium foam bar is in a range of 0.2–0.3 by rapid cooling of the pipe. To examine the ratio of deformation energy to weight of the pipe including the aluminium foam, a compression test using a press is carried out. The deformation energy of the pipe can be increased with aluminium foam filled by the proposed method.     

Methacrylate-based ionic liquid: radical polymerization/copolymerization with methyl methacrylate and evaluation of molecular weight of the obtained homopolymers

Azobisisobutyronitlite (AIBN)-induced free radical polymerization of a methacrylate-based ionic liquid monomer, 1-(2-methacryloxyethyl)-3-methylimidazolium bis(trifluoromethanesulfonyl)imide (Met-IL) was carried out in a common organic solvent, N,N-dimethylformamide (DMF), and an ionic liquid, 1-ethyl-3-methylimidazolium bis(trifluoromethanesulfonyl)imide (EMImTFSI). The molecular weight of the obtained poly(Met-IL) was evaluated by transforming it to non-ionic poly(methyl methacrylate) with hydrolysis of the imidazolium-salt-substituted pendant ester groups and methyl esterification. Radical copolymerization with methyl methacrylate (MMA) was also carried out in both DMF and EMImTFSI. Analysis of copolymer composition revealed that the reactivity of Met-IL was lower than that of MMA in both DMF and EMImTFSI solutions.     

Distributions of density and fission products in the reaction product between irradiated MOX fuel and molten zircaloy-2

Two- and three-dimensional images were obtained by X-ray CT in the reaction product between zircaloy-2 cladding tube and MOX fuel. The gamma-ray intensity distributions in the same specimen were also obtained by gamma-ray measurements of two fission products (Cs-137 and Eu-154) and one neutron-activated nuclide (Co-60). The average values of the fuel density (about 10.5 g/cm³) and the cladding density (about 6.55 g/cm³) were obtained in the metallic phase region by evaluation of the density distributions on two-dimensional X-ray CT images. The distributions of the crushed fuel pellet and the pores were also clearly observed in the three-dimensional X-ray CT images. The following results were found from the gamma-ray measurement. First, Cs-137 was observed in the unreacted fuel region and the pore region in the metallic phase region. Second, Eu-154 was widely distributed to all regions. Finally, Co-60 was confirmed only in the metallic phase region.