Effect of sulfur on synergistic corrosion behavior of Q235 and 16Mn steel in sodium aluminate solution

• Published in: Scientific reports 2024-09, Vol.14 (1), p.22301-13, Article 22301
• Main Authors: Li, Dongyu, Quan, Bianli, Li, Junqi, Chen, Chaoyi, Xu, Jun, Wang, Hanli
• Format: Article
• Language: English
• Subjects: 16Mn steel; 639/301; 639/638; Adsorption; Aluminum oxide; Corrosion; Corrosion mechanism; Dynamics; Electrochemistry; Ferric oxide; Humanities and Social Sciences; Iron oxides; Iron sulfides; multidisciplinary; Potentiodynamic polarization; Q235 steel; Science; Science (multidisciplinary); Steel; Sulfide; Sulfur; Sulfur content
• ISSN: 2045-2322; 2045-2322
• DOI: 10.1038/s41598-024-72639-x

In this study, the corrosion electrochemistry and corrosion behavior of two steels were studied under the simulated alumina production conditions. The corrosion rate of 16Mn steel is greater than that of Q235 steel. The effect of S 2− concentration on corrosion rate was significantly higher than that of S 2 O 3 2− . The synergistic corrosion rates of Q235 and 16Mn steels increase at first and then decrease with the sulfur content, and the peak value appears when the concentration of S 2− and S 2 O 3 2− is 4 g/L and 3 g/L respectively. There are two main types of corrosion products: one is surface octahedral grain, which is composed of Fe 2 O 3 , Fe 3 O 4 and Al 2 O 3 .The other is the interlayer corrosion between the surface layer and the matrix, which is composed of FeS, FeS 2 and NaFeO 2 .The formation mechanism of the corrosion and corrosion mechanism were obtained by analyzing the phenomenon of ion competitive adsorption. Further validation and analysis of ion competition adsorption phenomenon were conducted using first-principles calculations based on density functional theory (DFT). The formation of corrosion products on the steel surface was investigated at an ion level, and the adsorption energies of OH − and S 2− at the top site of Fe(110) surface were calculated. It was found that S 2− is more likely to be adsorbed on the Fe(110) surface compared to OH − . The corrosion mechanism of steel is discussed preliminarily.