Study on initial corrosion behavior of bogie steels with ferrite plus pearlite and granular bainite structures immersed in sulfur-containing environment

被引:3
|
作者
Song, Jialiang [1 ]
Zhang, Hao [1 ]
Yin, Chenghui [1 ]
Chen, Junhang [1 ]
Yu, Wei [2 ]
Zhou, Herong [3 ]
Wu, Junsheng [1 ]
Xiao, Kui [1 ]
机构
[1] Univ Sci & Technol Beijing, Inst Adv Mat & Technol, Beijing 100083, Peoples R China
[2] Univ Sci & Technol Beijing, Natl Engn Res Ctr Efficient Rolling, Beijing 100083, Peoples R China
[3] Wuhan Univ Sci & Technol, State Key Lab Refractories & Met, Wuhan 430081, Peoples R China
关键词
Bogie steel; Initial corrosion; Microstructure; Surface rust layer characteristic; Micro-galvanic effect; S-containing environment; WEATHERING STEEL; ATMOSPHERIC CORROSION; LOCALIZED CORROSION; RESISTANCE; MECHANISM; MARINE; MICROSTRUCTURE; TEMPERATURE; PROPAGATION; PERFORMANCE;
D O I
10.1016/j.jmrt.2024.01.263
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
The corrosion behavior of bogie steel with two different structures immersed in a sulfur-containing environment for 12 h was studied, including ferrite + pearlite structure (the heating temperature is 1473 K, the final rolling temperature is 1123 K, the final cooling temperature is 873 K, and the cooling rate is controlled at 7-9 K/s) and granular bainite structure (the heating temperature is 1223 K, keep warm for 2 h, cooling in water is 10 min, the cooling rate is greater than 100 K/s). The results show that there is no significant difference in the initial corrosion rate between ferrite + pearlite and granular bainite structures. The former is affected by the microregion galvanic effect and local residual stress to jointly promote corrosion initiation, while the latter has a uniform distribution of local residual stress on the surface, which is the main factor for corrosion initiation. After the sample is immersed, a dense thin rust layer quickly forms on the surface, blocking O-2 in the solution, resulting in the dissolution of the ferrite matrix of the two structures is mainly affected by the reduction of H+ and SO32-/SO42-.
引用
收藏
页码:2188 / 2203
页数:16
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