|
■■■■■■■■■■■■■■■■■■■ 川崎製鉄技報 KAWASAKI STEEL GIHO Vol. (1969) No.3 ■■■■■■■■■■■■■■■■■■■ |
| FeおよびFe−0.3％Cuの酸性硫酸塩水溶液中における分極挙動 The Polarization Behavior of Fe and Fe-0.3%Cu in Acidic Sulfate Solutions 後藤 実成(Minari Goto) 細田 博(Hiroshi Hosoda) |
| 要旨 : 0.5M(H2SO4＋Na2SO4)水溶液中におけるFeおよびFe−0.3％Cuのアノードおよびカソード分極挙動を定電位分極法で調べた。Fe中の0.3％Cuはアノード・カソード両分極の過電圧を著しく増すことがわかった。定常分極曲線をもとに，Fe−0.3％Cuのアノード溶解とカソード還元の反応速度式を求めた。両反応のTafel勾配と反応速度のpH依存性は純鉄の場合とほとんど等しく，カソード反応の活性化熱は純Feで12kcal/mol，Fe-.03％Cuで11.5kcal/molであった。したがって，FeとFe-0.3％Cuに関して反応機構は同じと思われ，Fe中に少量のCuを添加したことによる腐食速度の低下は反応点の減少によると推定される。Fe-0.3％Cuの腐食面には純Feでは見られない付着性の弱い黒灰色物質が生成するが，そのほとんどは非晶質物質で，他に微量のCu2Sが依存していることがＸ線回折で判明した。 |
| Synopsis : The anodic and cathodic polarization behavior of Fe and Fe-0.3%Cu has been investigated in 0.5M (H2SO4+Na2SO4) solutions by means of potentiostatic polarization method. 0.3%Cu contained in Fe was found to increase both the anodic and cathodic overvoltage remarkably. The reaction rate equations for the anodic dissolution and the cathodic reduction on Fe-0.3%Cu were determined from the results of the measurement of the steady state polarization curves. The anodic and cathodic Tafel slopes and pH dependencies of each reaction rate for Fe-0.3%Cu were almost coincident with those for pure Fe, and heats of activation for cathodic reactions on pure Fe and Fe-0.3%Cu are 12kcal/mol and 11.5kcal/mol, respectively. This coincidence of these values suggests that the anodic dissolution and the cathodic reduction for pure Fe and Fe-0.3%Cu should be based on the same mechanism. The decrease in corrosion rate by small additions of Cu to Fe may be explained by the decrease in number of reaction sites for the both reactions. Dark gray substance was found loosely adherent to the corroded surface in the case of Fe-0.3%Cu, absent in the case of pure Fe, which was confirmed to consist of certain amorphous substance and a small amount of Cu2S. |
| 本文（PDF: 10P/338kb） |