Synthesis of non-equilibrium phases in immiscible metals mechanically mixed by high pressure torsion

The structural changes in mechanically mixed metals of immiscible combinations of elements caused by bulk mechanical alloying (MA) through the use of high pressure torsion (HPT) were investigated in Ag–Ni and Nb–Zr systems. There was no alloying between Ag and Ni on atomic scale even after 100 rotations of HPT. On the other hand, the β-Zr phase started to appear after HPT 2 rotations in the Nb–Zr system, even though β-Zr is a high temperature phase. Further, Nb and Zr were completely mixed to form a bcc structured single phase after HPT 100 rotations. The sequence of alloying in the Nb–Zr system during HPT was discussed. These results clearly suggest that non-equilibrium phases can form in the Nb–Zr system by bulk MA by the use of HPT.     

Plasma treatment on electrode surfaces of bifacial silicon solar cells

To lower the fabrication cost of silicon solar cells, a surface treatment using a dielectric barrier discharge (DBD) instead of a wet cleaning technique was examined on electrode surfaces on silicon solar cells. The fill factor obtained through measuring current–voltage characteristics was evaluated, and the treated surface state was characterized by energy-dispersive X-ray. It was found that the DBD effectively activated the electrode surface and the surface treatment on finger electrodes contributed greatly to improve the fill factor.     

Improvement of Selectivity for Partial Hydrogenation of Benzene by Rare Earth Nitride Upon NH3 Treatment

For the liquid-phase partial hydrogenation of benzene at 483 K, the selectivity toward cyclohexene was greatly improved upon treating rare earth nitride with ammonia. For YbN obtained by thermal decomposition of Yb(NH₂)₂ at 1173 K, the selectivity of the NH₃-treated YbN was 75%, in contrast to nil for the untreated YbN.     

Switching of H∞ controller under constraints and decision of controller state at instance of the controller switching

In real control systems, certain constraints are placed on the input, state, and output values. If such constraints are violated, the system may become unstable, in a worst‐case scenario. One of the promising approaches to solving this problem is to switch the controller according to the state of the closed‐loop system. No useful design strategy for each controller, however, has yet been developed. In addition, the determination of the controller state at the instant of controller switching has not been investigated. First, this paper presents a new design methodology which merges the switching control and H_∞ controller design into one design algorithm. Second, this paper presents a way of determining the controller state at the instant of controller switching. Finally, the proposed method is applied to force control of a one‐DOF manipulator in order to demonstrate the usefulness of the proposed method. © 2002 Wiley Periodicals, Inc. Electr Eng Jpn, 142(2): 68–75, 2003; Published online in Wiley InterScience ( www.interscience.wiley.com ). DOI 10.1002/eej.10082     

Liquid-Phase-Assisted Sintering of Calcium-Doped Lanthanum Chromites

Investigations have been made on the low-temperature sinterability of calcium-doped lanthanum chromites which are to be used as interconnectors in solid oxide fuel cells (SOFCs). Nominally chromium deficient lanthanum calcium chromites (La_0.7Ca_0.3Cr₁-_yO₃, y = 0.02) were found to be sinterable to 94% theoretical density at 1573 K in air, whereas no densification was observed for samples with y = 0. The two-step shrinkage process suggests a liquid phase sintering mechanism with calcium oxychromates playing an important role as the liquid phase. After sintering at 1573 K, calcium-rich substances remained at grain boundaries.     

Thoracic vertebral bone metastasis from uterine leiomyosarcoma

We report a patient with solitary thoracic vertebral bone metastasis (Th 8) from uterine leiomyosarcoma. The vertebral metastatic lesion was treated surgically, and vertebral body replacement with ceramic prosthesis and anterior spinal stabilization were performed. Such aggressive surgical intervention for solitary vertebral bone metastasis may contribute to the improvement of prognosis and maintenance of general quality of life in the patient.     

Oxidation of ferrous iron by acidophilic iron-oxidizing bacteria from a stream receiving acid mine drainage

In this study, the oxidation of ferrous iron by the acidophilic iron-oxidizing bacteria was investigated by field survey and laboratory-scale batch and continuous experiments. The activity of the acidophilic iron-oxidizing bacteria was affected by pH, water temperature and concentration of glucose. The rate of oxidation of pyrite was accelerated by the acidophilic iron-oxidizing bacteria. The number of bacteria attached to the surface of a rotating biological disk changed with the ferrous iron loading.     

CO2 decomposition with oxygen-deficient Mn(II) ferrite

An oxygen-deficient Mn(II) ferrite (Mn_0.97Fe_2.02O_3.92) was synthesized and its reactivity to reduce CO₂ gas into carbon was studied at 300°C. The oxygen-deficient Mn(II) ferrite was obtained by flowing H₂ gas through Mn(II) ferrite with a nearly stoichiometric composition of Mn_0.97Fe_2.02O_4.00 at 300° C. The lattice constant of the oxygen-deficient Mn(II) ferrite (0.8505nm) is larger than that of the Mn(II) ferrite with a nearly stoichiometric composition (0.8498nm). The chemical composition of the Mn(II) ferrite changed from Mn_0.97Fe_2.02O_4.00 to Mn_0.97Fe_2.02O_3.92 during the H₂ reduction process, indicating that the oxygen is deficient in the spinel structure of the Mn(II) ferrite. This was confirmed by Mössbauer spectroscopy and X-ray diffractometry. The efficiency of CO₂ decomposition into carbon at 300°C with the oxygen-deficient Mn(II) ferrite was much lower by about 10⁵ than that of oxygen-deficient magnetite. This is considered to be due to the difference in electron conductivity between Mn(II) ferrite and magnetite, which determines the reductivity for CO₂ into carbon by donation of an electron at the adsorption site.     

Electrical properties and microstructure in the system ceria-alkaline earth oxide

The ionic conduction of oxygen in the ceria-alkaline earth oxide system was investigated as a function of temperature, partial pressure of oxygen and oxide composition, together with its crystal structure, density, and microstructure. Undoped ceria and its solid solution with alkaline earth oxides have a cubic fluorite structure. The ionic conductivity of ceria is greatly enhanced by additions of calcia and strontia, even when they are added in excess of the solubility limit. The conductivities of ceria-calcia and ceria-strontia were much higher than those of calcia-and yttria-stabilized zirconia. Up to the limit of calcia and strontia, the ionic transference number was nearly unity in the temperature range between 600 and 900°C. With an increase in calcia and strontia content, the ionic conductivity was little affected by the presence of a second phase of CaO and SrCeO₃.