Pit initiation in quenching and partitioning processed martensitic stainless steels
G. Li (TU Delft - Team Peyman Taheri)
Z. Li (TU Delft - Team Arjan Mol)
Ehsan Rahimi (TU Delft - Team Arjan Mol)
Marta Muratori (Acerinox Europa SAU)
Ali Smith (RINA)
Maria J. Santofimia Navarro (TU Delft - Team Maria Santofimia Navarro)
Yaiza Gonzalez Gonzalez Garcia (TU Delft - Team Yaiza Gonzalez Garcia)
More Info
expand_more
Other than for strictly personal use, it is not permitted to download, forward or distribute the text or part of it, without the consent of the author(s) and/or copyright holder(s), unless the work is under an open content license such as Creative Commons.
Abstract
The present article investigates the influence of chemical composition and phase fractions on the corrosion behaviour of industrially produced quenching and partitioning (Q&P) martensitic stainless steels. Localised corrosion was analysed by scanning Kelvin probe force microscopy (SKPFM) and scanning electrochemical microscopy (SECM) in 3.5 wt.% NaCl solution. SKPFM revealed a Volta-potential difference of around 40 mV between inclusions and the matrix, which is larger than the Volta potential variations within the matrix. This difference in surface potential is a driving force for selective dissolution (corrosion initiation) at inclusions and inclusion/matrix interfaces. SECM detected early pitting initiation, particularly in alloys containing MnS and TiN inclusions. Results suggest that pitting initiation and propagation occur at those specific regions. This study emphasised that irrespective of chemical composition and phase fraction, localised corrosion initiation in Q&P-processed martensitic stainless steels is predominantly governed by the presence of inclusions.