CORROSION ENGINEERING DIGEST
Online ISSN : 1884-1155
Print ISSN : 0010-9355
ISSN-L : 0010-9355
Volume 14, Issue 2
Displaying 1-7 of 7 articles from this issue
  • [in Japanese]
    1965Volume 14Issue 2 Pages 49-55
    Published: February 15, 1965
    Released on J-STAGE: November 25, 2009
    JOURNAL FREE ACCESS
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  • Zen-ichi Tanabe
    1965Volume 14Issue 2 Pages 56-59
    Published: February 15, 1965
    Released on J-STAGE: November 25, 2009
    JOURNAL FREE ACCESS
    Dealuminification in Cu-Al alloys is similar in mechanism to the dezincification that occurs in brass. Dealuminification was studied by means of accelerated immersion tests and anodic polarization measurements of various Cu-Al alloys, in which the content of Al was less than 12.4%. A mixed solution of 1/2mol CuSO4+1/3mol CH3COONa+1/3mol KCl+2/3mol CH3COOH(pH=3.3) was used in both cases.
    The results obtained were as follows:
    (1) Dealuminification current that is obtained by deducting the anodic current of Cu at -0.05V from that of each alloys at -0.05V corresponds to the dealuminification rate of its alloy.
    (2) Only α Cu-Al alloys have high resistivity to dealuminification.
    (3) Dealuminification is increased by the appearence of phases other than α phase.
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  • Takaaki Shimose, Akira Takamura, Hiroaki Hirose
    1965Volume 14Issue 2 Pages 60-65
    Published: February 15, 1965
    Released on J-STAGE: November 25, 2009
    JOURNAL FREE ACCESS
    Passivation and activation of titanium in deaerated non-oxidizing acid solutions were studied in order to investigate on the passivity of titanium. Critical potential for passivity and Flade potential shift towards noble direction with increasing chloride and hydrogen ion concentration, thus passivation becoming difficult. The critical potentials are expressed as E=E0+mlog[Cl-]-n(RT/0.4343F)pH, where R, the gas constant, T, absolute temperature, F, Faraday constant, E0 and m are constants. The constant n varies from 0.9 to 3.0 with environmental conditions such as temperature and kind of anion. Such different pH dependence of the critical potentials is attributed to the presence of different equilibrium surface reactions corresponding to passivation or activation for the respective corrosion conditions. The equilibrium reactions are considered to be
    Tia++2H2O=TiO2+4H++(4-a)e,
    2Tib++3H2O=Ti2O3+6H++(6-2b)e,
    Ti+2H2O=TiO2+4H++4e,
    2Ti+3H2O=Ti2O3+6H++6e.
    When the critical potentials expressed as equilibrium potentials of two former reactions, passivation or stability of passivity is affected directly by titanium ion. In such cases, as demonstrated for titanium-palladium alloy, corrosion resistance of titanium depends on the concentration of titanium ion in corrosive media.
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  • A. S. Couper, [in Japanese]
    1965Volume 14Issue 2 Pages 66-71
    Published: February 15, 1965
    Released on J-STAGE: November 25, 2009
    JOURNAL FREE ACCESS
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  • J. Kruger, H. T. Yolken, [in Japanese]
    1965Volume 14Issue 2 Pages 72-76
    Published: February 15, 1965
    Released on J-STAGE: November 25, 2009
    JOURNAL FREE ACCESS
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  • S. G. Vedenkin, V. S. Sinyabskii, [in Japanese]
    1965Volume 14Issue 2 Pages 76-79
    Published: February 15, 1965
    Released on J-STAGE: November 25, 2009
    JOURNAL FREE ACCESS
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  • J. C. Scully, T. P. Hoar, [in Japanese]
    1965Volume 14Issue 2 Pages 80-83
    Published: February 15, 1965
    Released on J-STAGE: November 25, 2009
    JOURNAL FREE ACCESS
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