Features of corrosion and inhibitory protection of steels in acid solutions containing iron(III) salts. Review

Y. Avdeev, A. V. Panova, T. Andreeva
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Abstract

A critical analysis of literature data on corrosion of steels in solutions of mineral acids containing Fe(III) salts and the possibility of inhibitory protection of steels in these environments has been carried out. The accumulation of Fe(III) salts in acid solutions during their operation at metallurgical, oil and gas enterprises, objects of housing and communal services is a result of dissolution of mineral deposits, scale, thermal scale, and rust containing Fe (III) compounds in them. In addition, additional oxidation of Fe(II) salts in acid solutions to Fe(III) compounds is possible. The effect of the redox potential, determined by the ratio of the content of Fe(III) and Fe(II) cations in them, as well as mobility of Fe(III) cations, on the corrosivity of the systems under consideration was examined. The reasons for the accelerating and retarding action of Fe(III) salts on corrosion of steels in acidic media were analyzed. Modern concepts of the mechanism of corrosion of steels in these environments are discussed. The low efficiency of the inhibitory protection of steels in mineral acids containing Fe(III) salts is demonstrated. It is noted that it is possible to increase the protective effect of some corrosion inhibitors (CI) in these environments by reducing their overall aggressiveness. It can be achieved by introducing H3PO4 into them, which is capable of binding Fe(III) into strong complexes that have a lower oxidizing capacity than Fe(III) aqua complexes and mobility in an aggressive environment. The CI used in an aggressive environment must be effective in slowing down not only the cathodic reduction of protons and anodic ionization of iron, but also significantly suppress reduction of Fe(III) cations, which is realized with the diffusion control. These requirements are met by composite CI based on triazoles, which in H2SO4 + H3PO4 and HCl + H3PO4 solutions containing Fe(III) salts are effective in slowing down the corrosion of low-carbon steel.
钢在含铁(III)盐的酸性溶液中的腐蚀和抑制保护特性。审查
对钢在含铁(III)盐的无机酸溶液中腐蚀的文献数据和钢在这些环境中抑制保护的可能性进行了批判性分析。在冶金、石油和天然气企业、住房和公共服务对象的酸性溶液中,铁(III)盐的积累是矿物沉积物、水垢、热垢和含有铁(III)化合物的铁锈溶解的结果。此外,铁(II)盐在酸溶液中额外氧化为铁(III)化合物是可能的。研究了氧化还原电位(由其中铁(III)和铁(II)阳离子含量的比例决定)以及铁(III)阳离子的迁移率对所考虑的体系的腐蚀性的影响。分析了铁(III)盐在酸性介质中加速和延缓钢腐蚀的原因。讨论了钢在这些环境中腐蚀机理的现代概念。结果表明,含铁(III)盐的无机酸对钢的抑制保护效率较低。值得注意的是,在这些环境中,一些缓蚀剂(CI)可以通过降低其整体侵蚀性来增强其保护作用。它可以通过引入H3PO4来实现,H3PO4能够将Fe(III)结合成强配合物,这些配合物的氧化能力比Fe(III)水合物低,并且在侵蚀环境中具有迁移性。在腐蚀性环境中使用的CI不仅要有效地减缓质子的阴极还原和铁的阳极电离,而且要显著抑制Fe(III)阳离子的还原,这是通过扩散控制来实现的。基于三唑的复合CI可以满足这些要求,在含Fe(III)盐的H2SO4 + H3PO4和HCl + H3PO4溶液中,复合CI可以有效减缓低碳钢的腐蚀。
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