Corrosion Activity of Stainless Steel SS430 and Carbon Steel B450C in a Sodium Silicate Modified Limestone-Portland Cement Extract

Stainless steel SS430 and carbon steel B450C were exposed for 30 days to the aqueous extract of sodium silicate-modified limestone-Portland cement as an alternative for the partial replacement of the Portland cement clinker. The initial pH of 12.60 was lowered and maintained at an average of 9.60, a...

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Detalhes bibliográficos
Autores: Bonfil, David, Veleva, Lucien, Feliú Jr., S., Escalante-García, José I.
Formato: artículo
Estado:Versión publicada
Fecha de publicación:2023
País:España
Recursos:Consejo Superior de Investigaciones Científicas (CSIC)
Repositorio:DIGITAL.CSIC. Repositorio Institucional del CSIC
OAI Identifier:oai:digital.csic.es:10261/341229
Acesso em linha:http://hdl.handle.net/10261/341229
Access Level:acceso abierto
Palavra-chave:Corrosion
Carbon steel
Stainless steel
Alkali-activated cement
Portland cement
Cement extract solution
Corrosion potential
pH
SEM-EDS
XPS
EIS
Descrição
Resumo:Stainless steel SS430 and carbon steel B450C were exposed for 30 days to the aqueous extract of sodium silicate-modified limestone-Portland cement as an alternative for the partial replacement of the Portland cement clinker. The initial pH of 12.60 was lowered and maintained at an average of 9.60, associated with air CO dissolution and acidification. As a result, the carbon steel lost its passive state, and the corrosion potential (OCP) reached a negative value of up to 296 mV, forming the corrosion layer of FeO, and FeOOH. In the meaning time, on the stainless steel SS430 surface, a passive layer of CrO grew in the presence of FeO, FeO and Cr(OH) corrosion products; thus, the OCP shifted to more positive values of +150 mV. It is suggested that a self-repassivation process took place on the SS430 surface due to the accumulation of alkaline sulfates on the interface. Because of the chloride attack, SS430 presented isolated pits, while on B450C, their area was extended. The quantitative analysis of EIS Nyquist and Bode diagrams revealed that the Rp of the corrosion process for SS430 was 2500 kΩcm, ≈32 times lower in magnitude than on B450C, for which the passive layer tended to disappear, while that on SS430 was ≈0.82 nm.