Journal of the Japan Society of Powder and Powder Metallurgy
Online ISSN : 1880-9014
Print ISSN : 0532-8799
ISSN-L : 0532-8799
Volume 9, Issue 3
Displaying 1-3 of 3 articles from this issue
  • (II) Studies on the Process of Reduction of Tungsten Trioxide
    Yungpil Ahn
    1962 Volume 9 Issue 3 Pages 93-101
    Published: June 25, 1962
    Released on J-STAGE: May 22, 2009
    JOURNAL FREE ACCESS
    The process of reduction of tungsten trioxide in both dry and wet hydrogen was studied by means of the weight loss measurement, the X-ray analysis, the surface area measurement and the observation by electronmicroscope. The results obtained are as follows.
    (1) The reduction rate differs from each stage of the reaction mentioned above and it also changes with the time duration of reduction. However, the reduction rate of α-tungsten oxide to metallic tungsten maintains a constant value until the reaction almost completes.
    (2) The average size of the tungsten particles produced by the reduction in hydrogen is affected mainly by the reduction temperature and also by the partial pressure of water vapor in hydrogen.
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  • Kiyoshi Tamura, Toru Takeda
    1962 Volume 9 Issue 3 Pages 102-108
    Published: June 25, 1962
    Released on J-STAGE: December 04, 2009
    JOURNAL FREE ACCESS
    With the object of atomizing high melting metals by some suitable design of jet using air, steam, water or other expansible fluid, the present authors newly designed ring-type atomizing nozzle, by which molten copper was atomized with air.
    In the present work, the effects of certain atomizing variables upon the characteristics of the produced copper powder and its particle size distribution have been examined.
    The results are as follows;
    1) When other atomizing variables remain constant, the peak of particle size distribution curve always occurs at the range of 40 to 50 microns in spite of increasing compressed air pressure.
    2) Molten copper atomized with air develops a powder the particles of which are substantially spherical, and this leads to powder of high apparent density-usually between 5.0 and to 5.5 g/cm3 and of good flow factor, -approximately 15 sec.
    3) The microstructure of the powder shows that copper atomized with air includes Cu2O and its concentration becomes higher with approaching outer surface, and also the smaller the particle size, the lower Cu2O concentration.
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  • Yasumasa Goto, Toshio Kitamura
    1962 Volume 9 Issue 3 Pages 109-113
    Published: June 25, 1962
    Released on J-STAGE: May 22, 2009
    JOURNAL FREE ACCESS
    The pressure versus temperature diagram of the chromium oxides (Cr2O5, CrO2 and Cr2O3) was determined by the closed vessel method in the range of higher oxygen pressures up to 600 atms. Chromium pentaoxide Cr2O5 is comparatively stable below 200°C, but it dissociates into CrO2 above this temperature. The stable ranges of CrO2 and Cr2O3 in the diagram are separated by the dissociation pressure curve of CrO2 which rises exponentially with increasing temperature through the points (450°C, 100 atms.) and (520°C, 600 atms.). The presence of Cr3O8, which had been reported to be stable at room temperature, was not confirmed above 200°C in the present experiments. The results of determination of oxygen contents in CrO2 phase indicate that this phase is non-stoichiometric; their composition varies from CrO1.92 to CrO2.02 depending on the equilibrium conditions. The ratio of O/Cr increases with the fall of temperature and incresing oxygen pressure. The lattice constants of CrO2+X (rutile type structure) decrease with increasing oxygen contents. The latter effect is quite consistent when we assume that the excess Cr ion are present as interstitials at the interlattice points of oxygen. The accurate lattice constants of stoichiometric compound CrO2 are found to be a=4.408, c=2.910 a.u., a/c=1.51. The saturation magnetization of CrO2+X at room temperature seems to increase with increasing O/Cr ratio. The ferromagnetic Curie point of them, how-ever, seems not to change with O/Cr ratio by more than 10°C.
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