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.

This work presents an investigation of the microstructure development during the application of the quenching and partitioning (Q&P) process to two stainless steels with different Mn content. The results are compared with calculations based on the constrained carbon equilibrium theory, paying special attention to the presence of reactions competing for the carbon available for partitioning and to the effect of alloying element segregation. Results show that chromium carbides must be considered when accounting for the carbon available for austenite stabilisation. Moreover, manganese/chromium segregation bands play an important role in the microstructure development, particularly in martensite formation, with important consequences in the microstructure development during the following processing steps.

Quenching & Partitioning (Q&P) steels owe their good strength-ductility combinations to the martensite/austenite (α’/γ) mechanical interactions and to the formation of mechanically-induced martensite (α′_mech) through the transformation-induced plasticity (TRIP) effect. An essential role is played by carbon, whose distribution among the phases can be modified through the Q&P route. This study presents a methodology to systematically and quantitatively examine the influence of the α’/γ mechanical interactions on the overall work hardening of the steel with respect to the role of carbon in the martensite. The methodology rests on the generation of a 3D micro-mechanical model that allows to derive, by crystal plasticity simulations, the overall response of a mechanically-stable α’/γ virtual microstructure. In combination with theoretical knowledge on hardening, the comparison between the experimental and simulated mechanical responses enables the quantification of the influence of the martensite carbon content and distribution on the overall TRIP strengthening contribution of the steel. The approach is applied to two low carbon Q&P-processed α’/γ microstructures of similar initial volume fractions of austenite and α′_mech formation kinetics with strain, but one containing a Nb-microaddition and displaying improved strength-ductility values. It is shown that the martensite strength and work hardening ability might additionally enhance or partially counteract the strengthening contribution from the austenite-to-α′_mech transformation during uniaxial loading. The results of this study highlight that the processing-dependent properties of the carbon-depleted martensite should be considered in the optimization of Q&P processed steels.