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In austenitic stainless steels, plastic deformation can induce martensite formation. The induced martensite is related to the austenite (γ) instability at temperatures close or below room temperature. The metastability of austenite stainless steels increases with the decreasing of stacking fault energy (SFE). In this work, the deformation induced martensite was analyzed by X ray diffraction, electron back scatter diffraction (EBSD), magnetic methods and atomic force microscope (AFM) in samples of a low SFE austenitic stainless steel, AISI 301LN and compared with a medium SFE stainless steel, AISI 316L. Both techniques, X ray diffraction and EBSD, presented similar quantities for the α'-martensite. Texture results indicate that the crystallographic orientation of the formed α'-martensite is {001}<110> and {103}<110>. The morphology of α'-martensite was analyzed by AFM. Corrosion tests showed that deformation reduces pitting corrosion and generalized corrosion resistance in both steels.

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O composto 5-(4-pyridinyl)-1,3,4-oxadiazole-2-thiol (Hpyt) adsorve espontaneamente sobre ouro formando SAMs ("Self-Assembled Monolayers") que, de acordo com os resultados eletroquímicos e de STM ("Scanning Tunneling Microscopy"), contêm poros através dos quais as moléculas dos complexos [Fe(CN) 6 ] 4-, a dependência da corrente faradáica com o pH da solução eletrolítica permitiu o cálculo do pKa da molécula de Hpyt adsorvida sobre ouro (4,2). Os parâmetros termodinâmicos, H ads and G ads , para o processo de adsorção desta molécula foram estimados em -20,01 e -39,39 kJ mol -1 , respectivamente, utilizando-se o modelo de Langmuir. O processo redox da metaloproteína citocromo c foi estudado utilizando-se a SAM de Hpyt. A constante de velocidade heterogênea de transferência de elétrons foi calculada em 2,29 10 -3 cm s -1 .5-(4-pyridinyl)-1,3,4-oxadiazole-2-thiol (Hpyt) spontaneously adsorbs on gold forming SAMs (self-assembled monolayers) that, based on STM (Scanning Tunneling Microscopy) and electrochemical data, contain pinholes through which [Fe(CN) 6 ] 4-and [Ru(NH 3 ) 6 ] 3+ probe molecules access the underlying gold electrode. For the former molecule, the dependence of the faradaic current on the electrolyte solution pH value allowed the evaluation of the surface pKa as 4.2. The thermodynamic parameters H ads and G ads for the Hpyt adsorption process could be described by the Langmuir model and were calculated as -20.01 and -39.39 kJ mol -1 , respectively. Electrodic redox reaction of cytochrome c metalloprotein was accessed by using the Hpyt SAM with a heterogeneous electron transfer rate constant of 2.29 10 -3 cm s -1 .