O2对L80-13Cr不锈钢在注水井环境中腐蚀行为的影响

    Effect of O2 on Corrosion Behavior of L80-13Cr Stainless Steel in Water Injection Well Environment

    • 摘要: 采用浸泡腐蚀试验,结合电化学测试分析,研究了O2对L80-13Cr在注水井环境中腐蚀行为的影响。结果表明,在含氧和不含氧的环境中,二者的平均腐蚀速率相近,含氧环境中的最大点蚀速率较大且表面点蚀坑更深。当溶液中存在O2时,钝化膜构成中出现一些疏松多孔的FeOOH、Fe3O4,并在表面分布着不均匀的粗大碳酸钙棒状晶粒,易构成氧浓差电池从而加剧L80-13Cr钢的局部腐蚀。O2的存在会使13Cr自腐蚀电流密度增大,吸氧腐蚀替代氢的去极化反应成为主要的阴极反应,进而加速阳极反应;且经7 d腐蚀后的钝化膜电阻值Rf和金属基体/膜界面的的电荷转移电阻Rct均比无氧环境下的低,含氧环境下的钝化膜的保护能力差,自修复能力弱,易发生稳态点蚀。

       

      Abstract: The influence of O2 on the corrosion behavior of L80-13Cr in water injection well environments was studied using immersion corrosion test combined with electrochemical testing analysis. The results show that the average corrosion rates of both oxygen containing and non oxygen containing environments are similar, and the maximum pitting rate in oxygen containing environment is larger and the surface pitting pits are deeper. When there is O2 in the solution, some loose and porous FeOOH and Fe3O4 appear in the passive film composition, and uneven coarse calcium carbonate rod like grains are distributed on the surface, which is easy to form an oxygen concentration cell, thus intensifying the local corrosion of L80-13Cr steel. The presence of O2 increase the self corrosion current density of 13Cr, and oxygen absorption corrosion replaces the depolarization reaction of hydrogen as the main cathodic reaction, thus accelerating the anodic reaction. Moreover, the resistance value of the passive film Rf and the charge transfer resistance Rct of the metal substrate/film interface after 7 d corrosion are both lower than those in the oxygen free environment. The passive film in the oxygen containing environment has poor protection ability and weak self-healing ability, and is prone to steady-state pitting corrosion.

       

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