Softening phenomenon by remilling of styrene–butadiene copolymer rubber–general-purpose polystyrene resin blend

The softening phenomenon by remilling of uncured blends of various commercia styrene—butadiene copolymer rubber (styrene content, 23.5 to 48 wt-%, styrene block 0 to 18 wt-%) with general-purpose polystyrene resin was mainly studied by examining the blend ratio dependence of hardness and compression modulus (in logarithmic form), with special attention to the state of dispersion of the polymers. It was found that the blend of styrene—butadiene copolymer rubber with general-purpose polystyrene resin forms a microheterogeneous polymer blend system and that the hardness and the compression modulus change in S-shaped curves versus blend ratio. However, the degree of softening phenomenon by remilling (roll surface temperature, 70°–90°C) was found to be different for the two blend systems, i.e., random styrene—butadiene copolymer rubber and block styrene—butadiene copolymer rubber. The softening phenomenon is more pronounced in random-type rubbers; and in some block-type rubbers, no softening phenomenon was observed. The influence of the styrene content of the polymer is small. Further discussions have shown us that the strong interaction between the polystyrene block of the copolymer and the styrene homopolymer of the general-purpose polystyrene resin controls the state of dispersion of polymers thereby causing this difference in the softening phenomena among the different kinds of styrene—butadiene copolymer rubbers.     

Study on high performance ice slurry formed by cooling emulsion in ice storage (discussion on adaptability of emulsion to thermal storage material)

This study focuses on an emulsion as a new thermal storage material for ice storage. Two types of emulsions were formed using an oil–water mixture with a small amount of additive. A silicone, light and lump oils were used. The water contents of the emulsions were 70, 80 and 90%. The additive was an amino group modified silicone oil. No depression of freezing point was observed for the emulsions because of their hydrophobic properties. In order to determine the structure of the emulsions, their electrical resistances were measured. Moreover, components of the liquids separating from the emulsions were analyzed. The results indicated that one emulsion was a W/O type emulsion, while the other was an O/W type. Finally, adaptability of the two emulsions to ice storage was discussed, it was concluded that a high performance ice slurry could be formed by the W/O type emulsion.     

金属注射成形冷作工具钢的超声疲劳性能

用超声疲劳试验研究了金属注射成形(MIM)冷作工具钢和锻轧钢(JIS SKD11)的高周疲劳性能。锻轧钢试样于423K回火1h。另一方面，为了评估回火温度对疲劳性能的影响，将MIM钢试样于不同温度下进行了回火。在N=103～108疲劳寿命范围内进行了超声疲劳试验。MIM钢试样的疲劳强度和锻轧钢试样相同。MIM钢试样的疲劳强度随着回火温度升高而减低。显微组织的观察结果表明，MIM钢试样的碳化物的直径与形状比锻轧钢试样的均一。     

Formation of Tetravalent Fe Ions in LaFeO3 Perovskite Through Mechanochemical Modification by Ball Milling

Mechanochemical modification of previously synthesized LaFeO₃ perovskite‐type oxide by a high‐energy ball milling was investigated to introduce Fe⁴⁺ ions or transform some Fe³⁺ into Fe⁴⁺ in LaFeO₃. X‐ray absorption fine structure studies revealed that the formation of Fe⁴⁺ ions into LaFeO₃ perovskite has been achieved at first time by ball milling at room temperature without any additives or replacement of La³⁺ ions by some divalent cations. The structural model of Fe⁴⁺ containing LaFeO₃ could be described as with a modified perovskite having equal amounts of La and Fe vacancies, which is supported by a good correlation between the results of Fe K‐edge XANES spectra and O₂‐TPD. The synthesis of Fe⁴⁺‐containing LaFeO₃ perovskite by ball milling was able to produce the O₂ adsorption capacity of nonsubstituted perovskite‐type oxide.     

Study on anisotropy of growth rate of ice crystal in supercooled water

The purpose of this research was to investigate the ice growth of a single crystal in three dimensions. Three-dimensional pattern of ice crystal growth in supercooled water was observed using Mach–Zehnder spectro-interferometer. Temperature was varied from −0.3 to −1.6 °C. It was found that the ice crystal began to grow as a single crystal at the tip of the capillary tube and propagated freely in supercooled water. Time variation of the shape of dendrite on a–c plane was obtained. It was found that half parabola fits the shape very closely, and the coefficient of squared term, a, of a quadratic function was calculated. The coefficient, a varied in time but at quasi steady state it was found to be depending mostly upon the degree of supercooling. Furthermore, the growth velocity in c-axis at the flat surface was calculated from the thickness measured. It was found that the velocity in c-axis is independent of the degree of supercooling but depends upon time, in other words, the thickness in c-axis.     

Mechanism of superconductivity in the polyhedral-network compound Ba8Si46

The silicon clathrates--materials composed of metal-doped Si(20) dodecahedra--were identified as the first superconductors based on pure silicon networks. The mechanism of superconductivity in these materials can be obtained by studying their phonon modes, as modified by isotope substitution, and specific-heat measurements. Here, we present experimental studies that provide strong evidence that superconductivity in Ba(8)Si(46) is explained in the framework of phonon-mediated Bardeen-Cooper-Schriefer theory. Analyses using the McMillan approximation of the Eliashberg equation indicate that the superconducting mechanism is in the medium coupling regime, but at the high-end limit. The large density of states at the Fermi level, which arises from hybridization of the Si(20) cluster and Ba orbitals, is responsible for the unexpectedly high superconducting temperature. The temperature evolution of the specific heat unambiguously shows that this is an s-wave symmetry superconductor.     

A Trial Thermal Rectifier

We have prepared a trial oxide thermal rectifier made of two cobalt oxides with different thermal conductivities based on a theoretical design. We created an experimental system to measure the thermal rectification and found that the rectifying coefficient defined by the ratio of heat current in a forward direction to that in the opposite direction was 1.43. We verified the thermal rectification by analyzing it quantitatively.     

Termini and main-chain composition of monomethoxy-terminated poly(ethylene glycol) studied by two-dimensional column chromatography

Samples of poly(ethylene glycol) especially those with functionalized ends have dimeric, trimeric, and tetrameric components at twice, three times, and four times as high a molecular weight (MW) as that of the main component. We used two-dimensional column chromatography to evaluate the MW and identify the terminal groups in each component. The first step is high osmotic pressure chromatography to prepare a sufficient amount of fractions that contain different percentages of the multimeric components. In the second step, each of the fractions was characterized by using regular size exclusion chromatography and high-resolution NMR. Decomposition of the chromatogram combined with isolation of the terminal methoxy peak in the NMR spectrum led to unique identification of the terminal groups. We thus found that the monomeric component is monomethoxy-terminated whereas the dimeric and other multimeric components are mostly dihydroxy-terminated.     

Influence of cocations on catalytic activity of copper ion-exchanged ZSM-5 zeolite for reduction of nitric oxide with ethene in the presence of oxygen

The coexistence of alkaline earth (Ca and Sr) and transition metal (Fe, Co and Ni) cations with Cu ions in ZSM-5 zeolite is effective in the promotion of the maximum activity and the expansion of the active temperature range for the reduction of nitric oxide with ethene in the presence of excess oxygen.     

Adsorption and photocatalytic decomposition of methylene blue on mesoporous metallosilicates

Mesoporous silica and mesoporous metallosilicates with Al, Ti and Fe as foreign metal species were successfully synthesized by the rapid room temperature method. Mesoporous metallosilicates with low contents of foreign metals possessed high surface area (S_a), large mesopore volume (V_mp) and highly ordered hexagonal mesoporous structure. Increases in foreign metal contents caused disordering the mesoporous structures and lowering the S_a and V_mp values. Bleaching of aqueous methylene blue (MB) by mesoporous silica and metallosilicates was investigated. Mesoporous aluminosilicate and ferrosilicate with cation-exchangeable ability showed the excellent property for the adsorption of MB of cationic dye, while mesoporous ferrosilicate and titanosilicate which absorbed UV lights catalyzed the photocatalytic decomposition of MB under UV-illumination.