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A Study on Flow-Accelerated Corrosion Mechanism of Low Alloy Tip- in Alkaline Solution using Rotating Cylinder Electrode

机译:旋转圆柱电极研究低合金尖头在碱性溶液中的流动加速腐蚀机理

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摘要

Activation and mass transfer process was studiedusing rotating cylinder electrode regarding the flow-acceleratedcorrosion of low alloy steel (ASME SA106 Grade C) in roomtemperature alkaline solution. The reducing agent diffusedeasily as rotating speed increased, and caused corrosionpotential to shift upward. Passive film formed from pH 9.8according to the mechanism of oxidation and subsequentprecipitation of ferrous species. Above pH 10.4, film formationprocess was active and stable. Corrosion current showedincrement with rotating velocity in pH 6.98, while it soonsaturated in above pH 9.8. On the other hand the limiting current,which governs pure mass transfer phenomenon of reducingspecies, increased with the rotating speed regardless of pH value.This indicates that activation reactions, which constituteoxidation of ferrous ion and formation of passive film on thebare metal surface, controls the entire corrosion process.
机译:利用旋转圆柱电极研究了低合金钢(ASME SA106 C级)在室温碱性溶液中的流动加速腐蚀,从而研究了活化和传质过程。随着转速的增加,还原剂容易扩散,并导致腐蚀电位向上移动。 pH值为9.8时形成的钝化膜,其氧化机理与随后发生的铁离子沉淀有关。在pH 10.4以上,成膜过程是活跃且稳定的。在pH值为6.98时,腐蚀电流随转速的升高而升高,而在pH 9.8以上时腐蚀电流很快饱和。另一方面,不管pH值如何,控制还原物种的纯质量传递现象的极限电流随旋转速度的增加而增加。这表明构成亚铁离子的氧化和在裸露的金属表面上形成钝化膜的活化反应控制着金属的氧化。整个腐蚀过程。

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