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Amorphous Fe±M±B (M¸Zr, Nb) based alloys with nanometer-sized crystallites have attracted attention due to their magnetic properties. Although corrosion resistance is a desirable property in such alloys, no study concerning this aspect has been reported. The eect of metalloid content and partial crystallization on corrosion resistance of Fe±M±B (M¸Zr, Nb) amorphous alloys, Fe 84 Nb 7 B 9 , Fe 84 Zr 7 B 9 and Fe 83 Zr 3X5 Nb 3X5 B 9 Cu 1 , was investigated. Corrosion resistance measurements were carried out by mass loss, potentiodynamic polarization, and thermogravimetric mass gain measurements. The partial crystallization of the amorphous alloy results in a decrease of the corrosion resistance for all the compositions analyzed. We also observed a greater corrosion resistance when Nb was present in comparison to the case when Zr was present. These results are an eect of the super®cial passive ®lm protector formed.

The biocompatibility of commercially pure (cp) titanium stems from its chemical stability within an organism, due to a fine film of impermeable titanium oxide covering the metal surface, which guarantees its resistance to corrosion. Despite its biocompatible characteristic, this material does not promote the formation of a hydroxyapatite layer, therefore, many research groups have sought to alter the material's surface, introducing modifications that might influence corrosion resistance. The electrochemical behavior of cp Ti, with hydroxyapatite coating and without hydroxyapatite coating, commonly used in implant materials, was investigated using an artificial saliva solution at 25 o C and pH=7.4. In the conditions of the study it was observed that the hydroxyapatite layer influences the properties of corrosion resistance. This study of the behavior of cp Ti with and without hydroxyapatite coating, in naturally aerated artificial saliva solution at 25 o C, was based on open circuit potential measurements and potentiodynamic polarization curves. At approximately 1x10 -6 A/cm 2 the potential for cp Ti with and without hydroxyapatite coating begins to increase at a faster rate, but at -74mV (SCE) for coated cp Ti and at 180mV (SCE) for uncoated cp Ti the increase in potential begins to slow. This behavior, characterized by a partial stabilization of current density, indicates that in those potential ranges a protective passive film is formed.