O objetivo do presente trabalho foi investigar o efeito do teor de carbono e nitrogênio em aços inoxidáveis ferríticos com 17%Cr (16%Cr-0,04%C-0,032%N; 17,2%Cr-0,02%C-0,0062%N; 18,5%Cr-0,008%C-0,0213%N) sobre o grau de sensitização (GS). Os aços foram solubilizados a 1200°C e resfriados em água. Tratamentos isotérmicos foram realizados a 600°C entre 5 minutos e 16 horas. Foi realizado o ensaio de reativação eletroquímica potenciodinâmica de ciclo duplo (DL-EPR) em solução 0,5M H2SO4 a (25 ± 2)°C. O GS foi medido através da relação entre as densidades de correntes anódicas máximas nas etapas de reversão, i r, e ativação, i a. O exame microestrutural dos corpos-de-prova foi realizado nos microscópios óptico e eletrônico de varredura após ataque metalográfico com reagente Vilella. Os resultados mostram variação do GS com o tempo. Um máximo de GS foi obtido para cada aço e, posteriormente, foi observada diminuição do GS. A intensidade do GS e o tempo de ocorrência variaram em função dos teores de carbono e nitrogênio nos aços.

The purpose of this work was to investigate the effect of carbon and nitrogen in 17%Cr ferritic stainless steels (16%Cr-0.04%C-0.032%N; 17.2%Cr-0.02%C-0.0062%N; 18.5%Cr-0.008%C-0.0213%N) on the degree of sensitization (DOS). These steels were solution annealed at 1200°C and quenched in water. Isothermal treatments were carried out at 600°C between 5 minutes and 16 hours. The Double Loop Electrochemical Potentiokinetic Reactivation test (DL-EPR) was carried out in a 0.5M H2SO4 solution at (25 ± 2)°C. The DOS was evaluated using a ratio between maximum anodic current density in reversion, i r, and activation, i a. The microstructural examination of specimens was carried out using optical and scanning electron microscopy after metallographic etching with Vilella's reagent. The results showed a DOS variation with time. Maximum values of DOS were obtained for each steel, followed by its reduction. The intensity of DOS and its kinetics vary in function of the carbon and nitrogen content in steels.

An apparatus to conduct high temperature erosion-oxidation studies up to 850 °C and with particle impact velocities up to 15 m.s-1 was designed and constructed in the Corrosion Laboratories of IPEN. The erosion-oxidation behavior of high velocity oxy fuel (HVOF) sprayed alloy and cermet coatings of Ni20Cr, WC 20Cr7Ni and Cr3C2 Ni20Cr on a steel substrate has been studied. Details of this apparatus and the erosion-oxidation behavior of these coatings are presented and discussed. The erosion-oxidation behavior of HVOF coated Cr3C2 25(Ni20Cr) was better than that of WC 20Cr7Ni, and the erosion-oxidation regimes have been identified for these coatings at particle impact velocity of 3.5 m.s-1, impact angle of 90° and temperatures in the range 500 to 850 °C.

In this investigation the corrosion resistance of four Al-Si hypereutectic alloys in a solution typical of condensate from automotive fuel combustion products, and referred to here as synthetic condensed automotive solution, has been studied. Three commercial alloys that are used for cylinder liners, and a laboratory made alloy, were studied by electrochemical impedance spectroscopy and measurements were taken after increasing times of immersion in this solution. Comparison of the electrochemical response of the four alloys in the corrosive solution was carried out. Although the mechanisms by which the four alloys corroded were similar, the results indicated differences in corrosion resistances of these alloys, and these differences could be related to their microstructures. The laboratory prepared alloy showed increased susceptibility to pitting corrosion compared to the commercial alloys. The surfaces of the alloys were examined, before and after the corrosion test, by scanning electron microscopy and analyzed by energy dispersive spectroscopy. The results indicated preferential attack of the aluminium matrix phase in all the alloys. The alloy with higher copper content and prepared by spray forming was more susceptible to pitting compared to the other alloys. The EIS response at low frequencies indicated a diffusion-controlled process, probably that of oxygen to the alloy interface.