KGa-priderite and related compound for the selective reduction of nitrogen monoxide with propylene

The catalytic activity of KGa-priderite, K_1.6Ga_1.6Ti_6.4O₁₆, and its related compound KGa₈Ga₉Ti₁₅O₅₆ was investigated for the selective reduction of nitrogen monoxide (NO) with propylene (C₃H₆) in the presence of high oxygen concentrations. The KGa-priderite showed significant activity during this reaction, but the related compound showed only a little activity. These compounds are quite different from the conventional catalysts for NO_x selective reduction and are characterized by the fact that their properties are free from the effects of solid acidity and support metals. This difference was attributable to the NO desorption rate at the surface of these compounds. It has become clear that the KGa-priderite catalyst remarkably adsorbed NO, and it is suggested that the amount of NO adsorbed and the amount of catalytic activity are able to be increased by the design of priderite structure.     

Relation between axial compressive strength of reinforcing fibres and fibre diameter

Attempts were made to estimate the fibre axial compressive strength of pitch-based graphitized and polyarylate fibres, and the relationship between the compressive strength and fibre diameter was investigated. The estimated compressive strength of fibres decreases with increasing temperature. This decrease in compressive strength may be accounted for by a decrease in the radial compressing force. There is a linear relationship between the estimated compressive strength and radial compressing force in a temperature range from room temperature to 80°C. The real compressive strength of the fibres, determined by extrapolating this straight line until the radial compressing force is zero, increases with decreasing fibre diameter, but remains almost unchanged at a diameter range smaller than 10 m. In order to obtain reinforcing fibres having a higher compressive strength, it will be necessary to prepare fibres having a diameter smaller than 10 m.     

Measurements ofPVTx properties of refrigerant mixture HFC-32+HFC-125 in the gaseous phase

The experimental 156PVTx properties of an important binary refrigerant mixture, HFC-32 (difluoromethane)+HFC-125 (pentafluorethane), have been measured for three compositions, i.e., 50, 60, and 80 wt% HFC-32, by a constant-mass-method coupled with expansion procedure in an extensive range of temperaturesT from 320 to 440 K, of pressuresP from 1.8 to 5.3 M Pa, and of densities p from 50 to 124 kg · m^–3. The experimental uncertainties of the present measurements are estimated to be within ±7 mK in temperature, ±2 kPa in pressure, ±0.2% in density and ±0.02 wt% of HFC-32. The sample purities are 99.998 wt% for HFC-32 and 99.99 wt% for HFC-125. Seventy-eight second and third virial coeflicients for temperatures from 320 to 440 K have been determined by the present measurements.Paper presented at the Twelfth Symposium on Thermophysical Properties, June 19–24, 1994, Boulder, Colorado, U.S.A.     

Pulse-Width Dependence in Current-Driven Magnetization Reversal Using GaMnAs-Based Double-Barrier Magnetic Tunnel Junction

We have investigated the current pulse width dependence on current-driven magnetization reversal in double-barrier structures using GaMnAs-based magnetic tunneling junctions (MTJ) in order to clarify the origin of low threshold current density for current-driven magnetization reversal. Comparing with the case of single-barrier MTJ, the pulse-width dependence reveals that threshold current density is reduced by double-barrier MTJ. We confirmed that the threshold current density in the order of 10⁴ A/cm² is estimated considering the effect of current pulse width.     

Preparation of porous sheet composite impregnated with TiO<Subscript>2</Subscript> photocatalyst by a papermaking technique

Titanium dioxide (TiO₂) powder-containing sheet composites, called TiO₂ sheet, were prepared by a papermaking technique, and their photocatalytic efficiency was investigated. The TiO₂ powders were homogeneously scattered over the fiber-mix networks tailored within the catalyst sheet. Under UV irradiation, the TiO₂ paper could decompose p-hydroxyacetophenone (p-HAP), although the degradation efficiency by the TiO₂ sheet was lower than that by the TiO₂ powder. Scanning electron microscopy revealed that coverage of the TiO₂ particles inside the sheet by alumina binder which was used to improve the sheet strength caused the deterioration of the photocatalytic performance. Internal addition of alumina binder made the TiO₂ sheet porous and such a TiO₂ sheet exhibited high photocatalytic performance equivalent to that of TiO₂ powder. The porous structure of TiO₂ sheet might contribute to effective transport of p-HAP to the surface of TiO₂ particles inside the sheet, resulting in high degradation performance. In addition, TiO₂ sheet prepared using TiO₂ sol showed higher photocatalytic efficiency than TiO₂ powder and it was indicated that the porous sheet structure might provide suitable conditions for TiO₂ catalysis for photodecomposition.     

Molecular dynamics study of deposition mechanism of cubic boron nitride

We have performed molecular dynamics simulations of bombardment of graphitic boron nitride (gBN) by energetic boron and nitrogen particles in order to examine the roles of ion bombardment in ion/plasma-assisted deposition of cubic boron nitride (cBN) thin films. We have found that the interaction of the energetic particles with gBN creates four-fold coordinated local structures (sp³-formation) inside gBN. We have also found that clusters of sp³-formations are created as a result of successive bombardment, some of which have cBN-like structures. On the basis of these results, we propose an atomic-scale model of cBN nucleation in which successive sp³-formation converts gBN into cBN.     

Efficient characterization for protein crystals using confocal Raman spectroscopy

Confocal Raman spectroscopy was applied to the characterization of various states emerging in the screening of protein crystallization. Four main characterized states, namely single crystals, microcrystals, precipitates, and clear drops without solid materials, appear in a droplet for crystallization; the first three states should be critically distinguished and characterized because of the limitations of visual observation under an optical microscope. Using lysozyme and other proteins, crystallization was performed by the hanging drop vapor diffusion technique and was monitored through an automated confocal Raman system. Prior to the spectroscopic analysis, an optical microscope with a charge-coupled device (CCD) camera and associated image processing software were used to rapidly identify the XY locations to be measured spectroscopically by focusing the laser beam on a test sample. Instead of the current image analysis by optical microscopy, confocal Raman spectroscopy with a high spatial resolution was used to identify the state of protein crystallization. Such real-time Raman monitoring also distinguished real protein crystals from pseudo-protein crystals emerging in a crystallization droplet.     

950 keV, 3.95 MeV and 6 MeV X-band linacs for nondestructive evaluation and medicine

We are developing compact X-band linac X-ray sources for nondestructive evaluation and medicine. First, we develop a portable X-ray system by a 950 keV 9.4 GHz X-band linac to realize on-site inspection. We use a low power (250 kW) magnetron as an RF source for compactness of the whole system. Since the RF power source is quite small and the stored energy in the structure is also small, we faced the problem of beam loading and current/RF-power oscillation. We are analyzing the problem by the circuit model. We plan to use this system for erosion inspection of metal pipes of petrochemical complex. By adopting a side-coupling cavity design to avoid the oscillation, we have developed 6 MeV X-band (9.3 GHz) linac for pinpoint dynamic tracking cancer therapy. Furthermore, we are manufacturing 3.95 MeV X-band (9.3 GHz) linac X-ray source with flexible waveguides for on-site bridge inspection. Updated results and situations are presented.     

Environmental protection: researches in National Institute of Radiological Sciences

Some studies for radiological protection of the environment have been made at the National Institute of Radiological Sciences (NIRS). Transfer of radionuclides and related elements has been investigated for dose estimation of non-human biota. A parameter database and radionuclide transfer models have been also developed for the Japanese environments. Dose (rate)-effect relationships for survival, growth and reproduction have been investigated in conifers, Arabidopsis, fungi, earthworms, springtails, algae, duckweeds, daphnia and medaka. Also genome-wide gene expression analysis has been carried out by high coverage expression profiling (HiCEP). Effects on aquatic microbial communities have been studied in experimental ecosystem models, i.e., microcosms. Some effects were detected at a dose rate of 1 Gy day(-1) and were likely to arise from interspecies interactions. The results obtained at NIRS have been used in development of frameworks for environmental protection by some international bodies, and will contribute to environmental protection in Japan and other Asian countries.     

Improvement of the photostability for YVO4:Bi,Eu nanoparticles synthesized by the citrate route

YVO₄:Bi³⁺,Eu³⁺ nanophosphor synthesized by the citrate route shows the photobleaching behavior, i.e., the decrease in photoluminescence intensity under the continuous irradiation of excitation light. This photobleaching property is remarkably suppressed by the washing post-treatment combined with centrifugation and the hydrothermal post-treatment. A relation between the fraction of photobleach and the amount of citrate ions coordinating to metallic ions at the surface of nanoparticles verifies that the photobleaching behavior of YVO₄:Bi³⁺,Eu³⁺ nanophosphor originates from the redox reaction between the citrate ions and V⁵⁺ in YVO₄ host crystal. The long-term light fastness test reveals that the hydrothermally treated YVO₄:Bi³⁺,Eu³⁺ nanophosphor has sufficient photostability for practical use over 15 years outside.