Present status of beryllides for fusion and industrial applications in Japan

Beryllides have remarkable characteristics besides their low density, such as high radiation resistance, high chemical stability, low hydrogen isotope retention and good high temperature mechanical strength especially for fusion applications. In order to have a practical usage for industrial applications, it is important to compile a set of quantitative data on such properties. It is also important to develop fabrication and processing paths to assure the processing of inherently brittle beryllides.The characterization and manufacturing technologies development have been carried out mainly on the Be₁₂Ti interemetallic compounds at the Be-rich side of the Be-Ti binary system. In the present paper, up-dated results on several properties are described for the compound fabricated by hot isostatic pressing (HIP) and ingot metallurgy. Mechanical properties of the compounds having a duplex microstructure with neighboring phases are evaluated by compressive tests from room temperature to 1273 K. Radiation damage of the compound is preliminary studied by charged particle irradiation. Oxidation in air and the interaction with water vapor are evaluated. Thermal desorption of the deuterium is examined by using transmission electron microscopy (TEM) and thermal desorption spectrometry (TDS). Through these evaluations it seems that Be₁₂Ti is superior as neutron multiplier with respect to pure Be metal.     

Thermodynamic calculation of phase equilibria of the Bi-Sn-Zn system

A thermodynamic assessment of the Bi-Sn-Zn ternary system was carried out by considering the experimental data including the phase equilibria and thermodynamic properties on the basis of the CALPHAD method. A set of optimized thermodynamic parameters has been obtained, which leads to a very good fit between calculation and experiments. In particular, the thermodynamic calculations in the Sn-rich portion are presented in view of the recent progress in Pb-free solder alloys.     

Environmental stress cracking of poly(acrylonitrile-butadiene-styrene)

The environmental stress cracking (ESC) of acrylonitrile-butadiene-styrene (ABS) copolymer caused by a non-ionic surfactant (poly-oxyethylene alkylether) was studied by constant-load tensile creep tests and edge crack tension (ECT) tests. The fracture surfaces were investigated by a scanning electron microscope (SEM) and the morphology of the crack tip was investigated by a transmission electron microscope (TEM). It was found that the results of the creep tests performed in the non-ionic surfactant were very different from those performed in air. SEM images of the fracture surfaces showed that there were three different mechanisms of fracture and that specimens had a tendency to rupture by ESC when the stress was small. The results of the ECT tests and the TEM images showed that the change in the mechanism of the fracture was attributable to the change of morphology at the crack tip.     

Corrosion resistance of structural materials in high-temperature aqueous sulfuric acids in thermochemical water-splitting iodine–sulfur process

Very harsh environments exist in the iodine–sulfur process for hydrogen production. Structural materials for sulfuric acid vaporizers and concentrators are exposed to high-temperature corrosive environments. Immersion tests were carried out to evaluate the corrosion resistance of ceramics and to evaluate corrosion-resistant metals exposed to environments of aqueous sulfuric acids at temperatures of 320, 380, and 460 °C, and pressure of 2 MPa. The aqueous sulfuric acid concentrations for the temperatures were 75, 85, and 95 wt%, respectively. Ceramic specimens of silicon carbides (SiC), silicon-impregnated silicon carbides (Si–SiC), and silicon nitrides (Si₃N₄) showed excellent corrosion resistance from weight loss measurements after exposure to 75, 85, and 95 wt% sulfuric acid. High-silicon irons with silicon content of 20 wt% showed a fair measure of corrosion resistance. However, evidence of crack formation was detected via microscopy. Silicon enriched steels severely suffered from uniform corrosion with a corrosion rate in 95 wt% sulfuric acid of approximately 1 g m⁻² h⁻¹. Among the tested materials, the ceramics SiC, Si–SiC, and Si₃N₄ were found to be suitable candidates for structural materials in direct contact with the considered environments.     

Use of multivariate analysis for the improvement in prediction accuracy of bacterial aerobic plate count by flow cytometry

Flow cytometry (FCM) and aerobic plate count (APC) by the culture method were performed on green tea samples spiked with Escherichia coli type strain NCTC9001 (ATCC11775) solutions of different concentrations. In FCM, fluorescence signals from multiple stained bacteria and other fluorophores are detected using detector channels, and recorded as events with a voltage at each channel. FCM data were analyzed in two ways: conventional and multivariate analysis. In the former, the number of events with voltages larger than the defined threshold values was regarded as the predicted APC. In the latter, voltage histograms of all channels were obtained and merged horizontally to serve as explanatory variables. Then a partial least squares regression (PLSR) model was built to predict APC from the histogram data. The coefficient of determination (R²) and the root mean square error (RMSE) between APC by the culture method and that predicted by conventional FCM were 0.916 and 1.08 cfu/ml². The APC values predicted by the PLSR model and those measured were in good agreement with R² of 0.982 and RMSE of 0.417 cfu/ml, which verified the potential of the proposed method for improving APC prediction accuracy by FCM.     

Performance improvement of the filter-type ‘transXend’ energy-resolving detector by considering noise sensitivity

The filter-type ‘transXend’ detector is an energy-resolving X-ray detector consisting of an energy-integrating flat-panel detector and multiple filters. In our previous studies, we have shown the effectiveness of the transXend detector, but the filters used were not optimized. To obtain better performance, the filters, especially their thickness and material, should be considered. In this paper, we present a method that can preliminarily estimate filter performance by comparing their noise sensitivity before carrying out numerous experiments. Two kinds of filter sets, Cu–Sn and W–Ag, with various thicknesses were evaluated. The results suggest that to image a 20-cm-thick object with 120-kV X-rays, an unfiltered channel and a channel filtered with 0.5-mm-thick Sn or 0.4-mm-thick Ag may be the best combination. The optimal filter thickness will be smaller if the object is thinner and the tube voltage is lower. For applications that require a wide dynamic range of detector response, a channel with a W filter may be better than an unfiltered channel. To verify the calculation results, computed tomography imaging experiments with a 3-cm-diameter phantom were also performed, and the experimental results showed good agreement with the calculation results.     

Experimental studies of optical Raman amplifiers for 1.3‐µm wavelength band and its application to 20 Gbit/s × 2 WDM transmission

Configurations of a Raman amplifier suitable for a 1.3‐µm wavelength band are discussed and their properties are experimentally investigated. Pump light with a wavelength of 1.23 µm that is necessary for the Raman amplification in the 1.3‐µm wavelength band is obtained using a 1.06‐µm fiber laser and Raman laser technique. Concerning the Raman laser, wavelength conversion from 1.06 µm to 1.23 µm is effectively achieved using a cavity configuration including fiber Bragg gratings and a dispersion‐shifted fiber. On the other hand, a conventional dispersion compensation fiber which has an essential property of high nonlinearity is applied in order to obtain large gain at 1.3 µm. Net gain of 35 dB and output power of 15 dBm are achieved. To confirm the applicability of the Raman amplifiers to high‐speed optical transmissions, experiments of 20 Gbit/s × 2 WDM repeaterless transmission through a 80‐km conventional single‐mode fiber are carried out. The 1.3‐µm signal should be degraded due to the dispersion caused by the dispersion compensation fiber in the Raman amplifier; However, bit error rate of less than 10 to 12 is obtained at both wavelengths, which is sufficient performance for practical uses. © 2003 Wiley Periodicals, Inc. Electr Eng Jpn, 143(1): 58–65, 2003; Published online in Wiley InterScience ( www.interscience.wiley.com ). DOI 10.1002/eej.10137     

Application of conventional activated carbon loaded with dispersed Pt to PEFC catalyst layer

Improvement of the polymer electrolyte fuel cell (PEFC) requires development of highly active electrodes of low cost to facilitate its widespread use. In the present study, the possibility of applying conventional activated carbon particles loaded with Pt to the electrode catalyst layer was tested because the particles were promising in dispersion of Pt and preparation cost. The catalyst layer was formed from the particles and Nafion® and was supported as a thin film on a rotating glassy carbon disk electrode (GC RDE). Activity for oxygen reduction was evaluated by the hydrodynamic voltammetry in perchloric acid to give a current free of the influence of mass transfer in the solution. Compared with a conventional catalyst layer formed from carbon black loaded with Pt, the new catalyst layer exhibited a significant, approximately 6-fold increase in current in the high potential region corresponding to a 100 mV increase in electrode potential. Activity, however, was retarded in the low potential region. This disadvantage was overcome by mixing a conductive agent into the layer and covering it with another layer containing carbon black loaded with Pt. This double catalyst layer exhibited increased activity across all potential regions, indicating the availability of the activated carbon in the electrodes.     

Low-Thermal-Expansion Properties of Sodium- and Lithium-Substituted Cubic Cesium Leucite Compounds

Cubic cesium leucite-based compounds, namely cesium leucites, cesium sodium leucites, and cesium lithium leucites, were synthesized using a multistep solid-state reaction method. The thermal expansion properties, in the temperature range of 298-1273 K, for the synthesized cubic cesium leucite-based compounds were examined using high-temperature powder X-ray diffractometry data. The thermal expansions of the cubic cesium leucite-based compounds were found to vary with the chemical composition. For instance, the thermal expansions of Cs_0.7Na_0.2Al_0.9Si_2.1O₆ and Cs_0.7Li_0.2Al_0.9Si_2.1O₆ were 0.14% at 1273 K and 0.081% at 1073 K, values lower than those of Cs_0.9Al_0.9Si_2.1O₆, which were 0.16% at 1073 K and 0.2% at 1273 K. The results showed that the thermal expansions of the cubic cesium leucite-based compounds changed with ionic substitution at the Cs⁺ sites because of ionic size differences between Cs⁺ and the Na⁺ or Li⁺ substitutional ions.