Duplex stainless steels have a large number of industrial applications and may replace high cost materials, especially in chloride-containing environments like seawater in off-shore platforms due to their high mechanical properties and good corrosion resistance. The influence of the ferrite content on the performance of duplex stainless steels in these corrosive environments is not well known. For the present paper, new superduplex stainless steels with ferrite between 30 and 60% were developed and their microstructure and corrosion resistance were evaluated by potentiodynamic polarization and electrochemical impedance spectroscopy (EIS) tests in NaCl 3.5% (wt %) at 26°C and 78°C. The results obtained at 26°C showed that the pitting potential (Epitt) is little affected by the ferrite content, but for the materials with higher ferrite it was possible to observe an increase in the repassivation potential with a decrease in the corrosion potential and passive currents due to the presence of more resistive passive films. Tests performed at 78°C indicated a high decrease in the Epitt for all the samples, independently of the ferrite percentage, although maintaining superiority in higher ferrite content. Alloys with a 55% ferrite phase content, i.e. less dependent of Ni element, present a superior performance of corrosion resistance.

INTRODUCTION: The mechanical properties and corrosion resistance of a material are dependent on its microstructure and can be modified by phase transformation. When a phase transformation occurs in a material it usually forms at least one new phase, with physical-chemical characteristics that differ from the original phase. Moreover, most phase transformations do not occur instantly. This paper presents an evaluation of the phase transformation of martensitic stainless steels ASTM 420A and ASTM 440C when submitted to different thermal processes. METHODS: Dilatometry tests were performed with several continuous heating and cooling rates in order to obtain the profiles of the continuous heating transformation (CHT) and continuous cooling transformation (CCT) diagrams for these two types of steel. Also, the temperature ranges for the formation of the different phases (ferrite and carbides; ferrite; austenite and carbides; non-homogeneous and homogeneous austenite phases) were identified. Rockwell hardness (HRC) tests were performed on all thermally treated steels. Anodic and cathodic potential dynamic polarization measurements were carried out through immersion in enzymatic detergent as an electrolyte for different samples submitted to the thermal processes in order to select the best routes for the heat treatment and to recommend steels for the manufacture of surgical tools. RESULTS: The martensitic transformation temperature tends to increase with increasing temperature for the initiation of cooling. The 440C steel had a higher hardness value than the 420A steel at the austenitizing temperature of 1100 °C. Above the austenitizing temperature of 1100 °C, the material does not form martensite at the cooling rate used, which explains the sharp decline in the hardness values. CONCLUSION: The study reported herein achieved its proposed objectives, successfully investigating the issues and indicating solutions to the industrial problems addressed, which are frequently encountered in the manufacture of surgical instruments.

This work reports results of studies on the electrochemical and structural properties of a Ti/Zr-based metal hydride alloy covered by Ni and LaNi4,7Sn0,3 powder additives by ball milling. The effect of this treatment is investigated for the activation time, hydrogen storage capacity and equilibrium pressure, cycling stability and the hydration/dehydration kinetics. Charge and discharge cycles show a significant decrease of the activation time due to an increase of the active area caused by the milling treatment, independent of the additive. However, other results have evidenced little effect of the milling surface treatment on the charge storage capacity, hydrogen equilibrium pressure, and hydration/dehydration kinetics, for both the Ni and LaNi4,7Sn0,3 covered materials.