Journal of the Metal Finishing Society of Japan
Online ISSN : 1884-3395
Print ISSN : 0026-0614
ISSN-L : 0026-0614
Volume 9, Issue 10
Displaying 1-7 of 7 articles from this issue
  • [in Japanese], [in Japanese]
    1958Volume 9Issue 10 Pages 361-365
    Published: October 20, 1958
    Released on J-STAGE: October 30, 2009
    JOURNAL FREE ACCESS
    Zinc immersion treatment on the surface of aluminium alloys was investigated, for the purpose of fixing the conditions for commercial operation as follows:
    (a) Alkaline solution
    NaOH (Sodium hydroxide) 120-525g/l ZnO(Zinc oxide) 20-100g/l
    Temperature 5-25°C Suitable for Al-Siand Al-Cu-Si
    (b) Acid solution
    ZnSO4 (Zinc sulfate) 500-750g/l HF (48% vol) (Hydrofluovic) 0.5-1.5cc/l
    Temperature 10-25°C Suitable for Al-Mg
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  • Hideo NAGASAKA, Takeshi TAKEI
    1958Volume 9Issue 10 Pages 365-370
    Published: October 20, 1958
    Released on J-STAGE: October 30, 2009
    JOURNAL FREE ACCESS
    As reported previonsly, internal stress in flame sprayed procelain enamel coating is larger than that in ordinary baked coating, and by this reason, the flame sprayed porcelain enamel coating is more sensitive for mechanical and thermal schock.
    In order to avoid this defect, the authors tried to improve the method of spraying and got the following results.
    1. By spraying at high temperature (650-750°C), moderately thick intermediate layer is formed between base and coating and the coating is adherent and stands schock as ordinary baked coating.
    2. By the addition of pyrophyllite in the flit, and by shortening the time of melting, good adherent coating is obtained. This is due to the reduction of internal stress in the coating.
    3. By the application of very brittle flit as under coating, shock-resistant adherent coating is obtained. This seems to be due to cusioning action of crack in the under coating.
    4. It is possible to spray porcelain enamel on the old coating. But, in this case, operator should be done with great carefulness in order to avoid crazing, chipping and fishscaling.
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  • Masao MUKAI, Yoshio KAWAI, Shiroh UEDA
    1958Volume 9Issue 10 Pages 371-375
    Published: October 20, 1958
    Released on J-STAGE: October 30, 2009
    JOURNAL FREE ACCESS
    Phosphating practice has been much improved in the bath composition. Heretofore some nitrates have been used as accelerator by adding to the conventional phosphating bath, however, there have appeared the chlorate-acceleraters in the recent literatures and patents. The result of investigation on this new method of chlorate-accelerated phosphating bath is reported in the present paper.
    Some of the behaviours of the bath in solution and the properties of the phosphate coatings were observed. In summary, the followings are proposed:
    1) The suitable compositions of the bath are
    Zinc powder 5-8g/l Acetic acid 3-8g/l
    Phosphoric acid 30-45g/l Potassium chlorate 1-3g/l
    Caustic soda 3-4g/l
    2) This solution exhibits a milky turbid colour followed by development of colloidal suspension, which hardly appears in the solution of composition range under 0.3% KClO3.
    3) The deposition of fine grained phosphate-coating on the steel surface dipped in the bath's, completed in 15min. at 50-60°C.
    4) The thickness of coating is about 17μ and the spontaneous electrode potential in 3% NaCl solution of the coating formed by this method, is nobler than that of the coating formed by the conventional method. Therefore, the coating of the former seems to be more anticorrosive than the later.
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  • Studies on Platinum Plating (3)
    Nobuteru AWA
    1958Volume 9Issue 10 Pages 376-379
    Published: October 20, 1958
    Released on J-STAGE: October 30, 2009
    JOURNAL FREE ACCESS
    (1) Even if (NH4)2HPO4 is added more than 30g the current density and depositing quantity do not increase.
    (2) If Na2HPO4·12H2O is added more than 300g the current density and depositing quantity decrease.
    (3) If much (NH4)2HPO4 is added brightness of plating surface immediately fade away.
    (4) Influence of Na2HPO4·12H2O on brightness of plating surface is very small.
    (5) As plating time goes on color of plating surface changes to light brown, then to brown and then to black.
    (6) The platinum amount of electrodeposition increases with a decrease in pH value in the plating solutions, More than 12.3pH, plate hardly. When the pH value becomes over 12.3 platinum is not deposited.
    (7) When the plating solution of lower pH values is used, the brightness of plating surface soon fades away.
    (8) That the color of plating surface changes to black is accounted for the electrodeposition of platinum black.
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  • [in Japanese], [in Japanese], [in Japanese]
    1958Volume 9Issue 10 Pages 380-382
    Published: October 20, 1958
    Released on J-STAGE: October 30, 2009
    JOURNAL FREE ACCESS
    Download PDF (794K)
  • [in Japanese]
    1958Volume 9Issue 10 Pages 383-387
    Published: October 20, 1958
    Released on J-STAGE: October 30, 2009
    JOURNAL FREE ACCESS
    Download PDF (730K)
  • [in Japanese]
    1958Volume 9Issue 10 Pages 388-394
    Published: October 20, 1958
    Released on J-STAGE: October 30, 2009
    JOURNAL FREE ACCESS
    Download PDF (938K)
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