Surface characterization and catalytic properties of La1−x -Sr x CoO3

The surface chemical states of the perovskite-type compounds, strontium doped lanthanum cobalt oxides (La_1?x Sr _x CoO₃), have been investigated using X-ray photoelectron spectroscopy (XPS). Catalytic oxidations of both methane and CO have also been investigated using flow methods. The chemical composition of the surface of La_1?x Sr _x CoO₃ was very different from that in the bulk, which was measured by X-ray fluorescence spectroscopy (XRFS). The catalytic activity of La_1?x Sr _x CoO₃ increased with an increase in the quantity of cobalt atoms on the surface.     

Photoinduced bidirectional phase transitions in single crystals of polydiacetylenes

Photoinduced phase transitions have been observed between the two phases in single crystals of polydiacetylenes with side-groups of alkylurethanes. The threshold of the excitation intensity for the photochromism is extremely low, one absorbed photon per 140 repeated backbone units, indicating a collective nature of the photoconversion. The excitation spectra for the converted fraction clearly show that the photoinduced phase transition is mediated by photogeneration of polaronic species and not of singlet excitons.     

Far-Infrared Reflection Spectra of Dielectric Ceramics for Microwave Applications

Far-infrared reflection spectra of dielectric ceramics, BaSm₂Ti₅O₁₄, BaTi₄O₉, and some pcrovskites such as Ba(Zn_1/3Nb_2/3)O₃, have been measured at room temperature using a Fourier transform infrared spectrometer in order to investigate the effect of the crystal structure on the dielectric properties. As for perovskites, Sr(Zn_1/3Nb_2/3)O₃ and Sr(Mg_1/3Nb_2/3)O₃, in which B site ions are ordered, were also measured. Reflectance data were analyzed by means of a factorized form of dielectric functions instead of the classical dispersion theory, and all of the spectra were well fitted. The values of dielectric constants and tan δ calculated from the reflectance data were in good agreement with resonant cavity measurements at 5 GHz. Furthermore, results of this study have shown that the main contribution to the microwave dielectric properties is caused by low-frequency optically active modes located at 50 to about 300 cm⁻¹, and for perovskite structures it is suggested that the ordering of B site ions is significant in obtaining low dielectric losses.     

A reconfigurable VLSI-based double-lens tracking camera

Watching and tracking an object while seeing a much wider view is one of advantages of the eye system. We proposed and developed a tracking camera system that mimics the eyes by using double-lens modules. In the system, a wide view is captured through the wide-lens module, while the target in it is tracked and magnified through the telescopic lens module. Electronic circuits for tracking control are implemented onto the reconfigurable VLSI or FPGA in order to embed the parallelism in the tracking algorithm into the hardware. A successfully developed FPGA-based prototype performs high-speed tracking at the video-rate. This work was present in part at the 12th International Symposium on Artificial Life and Robotics, Oita, Japan, January 25–27, 2007     

连铸中间包内三维湍流流动的数值模拟

连铸中间包的操作条件决定了其内流动现象的复杂性，为此，本文选择两种不同的湍流模型ｋ－ε和ＬＥＳ（Ｌａｒｇｅｅｄｄｙｓｉｍｕｌａｔｉｏｎ），建立了描述连铸中间包内三维湍流流动的数学模型，并实施了数值计算和模型验证，对单流中间包内的流动现象进行了描述，考察了有，无流动控制情况下中间包内的流动特征和湍流模型的合理性，结果表明，合理的流动控制有利于中间包内非金属夹杂的上浮和吸附，用ｋ－ε模型基本上能够描述     

Influence of activated carbon pore structure on oxygen reduction at catalyst layers supported on rotating disk electrodes

Carbon materials are often used as catalyst supports, and for catalysts in electrodes of a polymer electrolyte fuel cell, carbon black has been used. Recently, it was found, however, that activated carbon could replace carbon black and besides, significantly improve the activity of the electrode catalyst layer for oxygen reduction. In the present study, to optimize the pore structure of activated carbon for further activity improvement, the influence of the pore structure on the activity was investigated using activated carbon of various specific surface areas and mean pore diameters. A catalyst layer was formed from activated carbon loaded with platinum and a polymer electrolyte. The activity of the layer was measured in an oxygen-saturated perchloric acid solution, supporting the layer on a rotating glassy carbon disk electrode. We found that increases in the specific surface area and mean pore diameter increased the activity and that the latter was more effective than the former mainly due to the enhanced mass-transfer in the pores; the catalyst layer formed from activated carbon with the largest mean pore diameter was the most active. Unless pores excessively develop and lose connections between particles, a large pore diameter is therefore desired for the fuel cell electrodes.