Preparation of TiB2 sintered compacts by hot pressing

A sintered compact of titanium diboride (TiB₂) was prepared by hot pressing of the synthesized TiB₂ powder, which was obtained by a solid-state reaction between TiN and amorphous boron. Densification of the sintered compact occurred at 20 MPa and 1800° C for 5 to 60 min with the aid of a reaction sintering, including the TiB₂ formation reaction between excess 20 at % amorphous boron in the as-synthesized powder (TiB₂ + 0.2B) and intentionally added 10 at % titanium metal. A homogeneous sintered compact of a single phase of TiB₂, which was prepared by hot pressing for 30 min from the starting powder composition [(TiB₂ + 0.2B) + 0.1 Ti], had a fine-grained microstructure composed of TiB₂ grains with diameters of 2 to 3 m. The bulk density was 4.47 g cm^–3, i.e. 98% of the theoretical density. The microhardness, transverse rupture strength and fracture toughness of the TiB₂ sintered compact were 2850 kg mm^–2, 48 kg mm^–2 and 2.4 MN m^–3/2, respectively. The thermal expansion coefficient increased with increasing temperature up to 400° C and had a constant value of 8.8 x 10^–6 deg^–1 above 500° C.     

Synthesis of TiB2 powder from a mixture of TiN and amorphous boron

TiB₂ powder was synthesized by solid state reaction using amorphous boron and TiN as a source of titanium. The TiB₂ formation did not occur at all in a nitrogen atmosphere even at 1400° C. TiB₂ formed above 1100° C in argon and hydrogen atmospheres. The only crystalline phase of TiB₂ powder was favourably synthesized at 1400° C for 360 min in an argon atmosphere from a starting powder with a composition containing excess boron (B/Ti = 2.2). The synthesized powder was well dispersed and had a particle size of 0.5 to 2 µm. The powder activity was evaluated by sintering at 4 G Pa and 1300 to 1600° C for 15 min.     

电话自动计费集中管理系统的设计与实现

论述了基于电话网的电话自动计费器集中管理系统及配套作用的电话计费器的设计思想。     

Development of a 400 kJ Nb3Sn superconducting magnet for an SMES system

An Nb₃Sn superconducting magnet to store 400 kJ was developed as a unit magnet for a 2.4-MJ SMES system used for stabilization studies of electrical power systems. The superconducting magnet consists of a cryostat and an Nb₃Sn coil. The dimensions of the coil are: 340 mm inner diameter, 700 mm outer diameter and 177 mm axial length. The pool-cooled coil is a stack of 20 Nb₃Sn double pancakes, and the cooling channels are aligned between pancake coils. To reduce Joule loss in electrical power converters, the maximum operating current of the coil is designed to be 350 A, which is one order of magnitude less than the operating currents of similar scale coils for pulse use. The conductor is an Nb₃Sn monolithic conductor with cross section 1.50 × 2.38 mm. For good superconducting stability and high dielectric strength of the coil, the Nb₃Sn double pancakes were wound by the react-and-wind technique. Operation of dc current to 105% (367.5 A) of the design operating current was achieved without quench. After the whole of the coil was exposed out of liquid helium, the coil did not quench under 120 A current operation for more than 2 hours. It was verified that the coil was stable for the SMES system. © 1998 Scripta Technica, Inc. Electr Eng Jpn, 121(3): 44–52, 1997     

Reaction control of TiB2 formation from titanium metal and amorphous boron

TiB₂ powder was synthesized by a controlled formation reaction from titanium metal and amorphous boron. Precursory TiB₂ formed by the pretreatment of the mixed powder (mole ratio: B/Ti=2.0) at 600° C for 60 min in an argon stream. Hollow TiB₂ powder with an average grain size of 15m was obtained by subsequent heat treatment above 900° C for more than 60 min in an argon stream. The formation reaction of TiB₂ powder was further controlled by pretreatment of the mixed powder at 600° C for 60 min in a hydrogen and argon stream and subsequent heat treatment at 1000° C for 360 min in an argon stream, when hollow-free TiB₂ powder was formed by a milder formation reaction between amorphous boron and the reformed titanium metal with hydrogen diffused lattice.     

Mass transfer in polycrystalline ytterbium monosilicate under oxygen potential gradients at high temperatures

Mass transfer in polycrystalline Yb₂SiO₅ wafers with precise composition control was evaluated and analyzed by oxygen permeation experiments at high temperatures using an oxygen tracer. Oxygen permeation proceeded due to mutual grain boundary diffusion of oxide ions and Yb ions without synergistic effects such as acceleration or suppression. The oxygen shielding properties of Yb₂SiO₅ were compared with those of the other line compounds such as Yb₂Si₂O₇ and Al₂O₃ based on the determined mass transfer parameters. It was found that the more preferentially an oxide ion diffuses in the grain boundary compared to the interior of the grain, the greater the effect of suppressing the movement of the oxide ion by applying an oxygen potential gradient becomes.     

Electronic structures of polyacenacene and polyphenanthrophen anthrene. Design of one-dimensional graphite

The electronic structures of polyacenacene (PAA) and its geometrical isomer, polyphenanthrophenanthrene (PPhP) have been studied using the tight-binding SCF-CO (self consistent field-crystal orbital) method with respect to a design of one-dimensional (1D) graphite. The geometry of each polymer is optimized from the energetic point of view. It has been found that from the analysis of the electronic structure of its optimized geometry, PAA favours the structure without the carbon-carbon bond alternations, yielding no band gap. In this sense, PAA is a typical 1D-graphite. On the other hand, it is predicted that the magnitude of the band gap of PPhP in its optimized geometry is almost equal to that of trans-polyacetylene.     

Compensation Schemes for Resettlers in Indonesian Dam Construction Projects

Abstract

The performance of previous involuntary resettlement schemes for dam construction projects leaves much to be desired. The question to be asked is whether the present policy of development aid agencies is appropriate for countries where more dams will be built. This study examines the applicability of Japanese “soft technologies” to determine whether the existing policy is really instrumental in mitigating impacts. The study was carried out through analysis on Saguling and Cirata dam construction projects on the island of Java, Indonesia, in which 3,038 and 6,300 families were resettled, respectively. The emphasis of resettlement plans for these dams was on transmigration and aquaculture. The following findings were made: land-for-land policy was not fully met; transmigration schemes did not work as planned; resettlers failed to enjoy the benefits from aquaculture development fully due to the high capital needed; employment by dam construction projects was limited; and insufficient capital and training prevented resettlers from enjoying profits from secondary development. Lessons learned included: some mechanism should have been established for those who changed jobs from agriculture to other sectors; provision of urban land rather than farmland, as has been practised in Japan, should have been considered; and establishment of funds, as practised in Japan, should have been pursued. Such funds may be used for enhancing the infrastructure of the project area to promote secondary development for the purpose of creating new jobs for resettlers. It may also meet unexpected expenditures incurred after completion of a dam. Funds could also be utilized to give construction firms monetary incentives to employ resettlers. The creation of funds may be instrumental in safeguarding job security of resettlers.     

Oxygen permeation mechanism in polycrystalline mullite at high temperatures

The oxygen permeability of polycrystalline mullite wafers, serving as a model environmental barrier coating layer on SiC fiber‐reinforced SiC matrix composites, was evaluated at temperatures above 1673 h with an oxygen tracer gas (¹⁸O₂). Oxygen permeation occurred by grain‐boundary (GB) diffusion of oxygen from the high oxygen partial pressure (high‐Po ₂) surface to the low‐Po ₂ surface, with simultaneous GB diffusion of aluminum in the opposite direction. This GB interdiffusion of both oxygen and aluminum proceeded without acceleration or retardation, maintaining the Gibbs‐Duhem relationship. Oxygen permeation related to the GB diffusion of silicon was negligibly small compared to that generated by aluminum GB diffusion, resulting in decomposition of the mullite near the low‐Po ₂ surface. The GB diffusion coefficients for oxygen in the vicinity of the high‐Po ₂ surface were determined directly from the SIMS‐¹⁸O line profiles along individual GBs, as assessed from cross sections of the exposed wafer. The coefficients thus obtained were comparable to those determined in the absence of an oxygen potential gradient and those calculated from an oxygen permeation trial under the assumption of nearly ionic conductivity.