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Effect of Dissolved Oxygen and Immersion Time on the Corrosion Behaviour of Mild Steel in Bicarbonate/Chloride Solution

机译:溶解氧和浸入时间对低碳钢在碳酸氢盐/氯化物溶液中腐蚀行为的影响

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摘要

The electrochemical behavior of mild steel in bicarbonate solution at different dissolved oxygen (DO) concentrations and immersion times has been studied under dynamic conditions using electrochemical techniques. The results show that both DO and immersion times influence the morphology of the corrosion products. In comparative tests, the corrosion rate was systematically found to be lower in solutions with lower DO, lower HCO3 concentrations and longer immersion time. The SEM analyses reveal that the iron dissolution rate was more severe in solutions containing higher DO. The decrease in corrosion rate can be attributed to the formation of a passive layer containing mainly α-FeO (OH) and (γ-Fe2O3/Fe3O4) as confirmed by the X-ray diffractometry (XRD) and X-ray photoelectron spectroscopy (XPS). Passivation of mild steel is evident in electrochemical test at ≈ −600 mVSCE at pH  ≥ 8 in dearated ( ≤ 0.8 ppm DO) chloride bicarbonate solution under dynamic conditions.
机译:在动态条件下,使用电化学技术研究了低碳钢在碳酸氢盐溶液中不同溶解氧(DO)浓度和浸入时间的电化学行为。结果表明溶解氧和浸入时间均会影响腐蚀产物的形貌。在对比试验中,系统地发现在溶解氧较低,HCO3 -浓度较低且浸泡时间较长的溶液中,腐蚀速率较低。 SEM分析表明,在溶解度较高的溶液中,铁的溶解速率更为严重。 X射线衍射仪(XRD)和X射线光电子能谱仪(XPS)证实,腐蚀速率的降低可归因于形成了主要包含α-FeO​​(OH)和(γ-Fe2O3/ Fe3O4)的钝化层。 )。低碳钢的钝化在动态条件下,在昂贵的(≤0.8 ppm DO)氯化氢碳酸氢盐溶液中,在pH≥8的≈-600 mVSCE的电化学测试中明显可见。

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