Electrochemical Corrosion Behaviour of Stainless Steels AISI 304 and 316L in Caribbean Sea Water

2015 ◽  
Vol 227 ◽  
pp. 95-98
Author(s):  
D.M. Herrera-Zamora ◽  
Lucien Veleva ◽  
Juan Luis López

AISI 304 and 316L flat samples were exposed during 3 months in Carribean sea water.At the end of the experiment Ecorrof AISI 316L reached one-half the negative potential value than that of AISI 304. The tendencies of Ecorrwere correlated with the pitting corrosion development. They could be considered as a consequence of the opposition between the nucleation of new pits and repassivation of active sites. The analysis of Ecorrfluctuations was carried out with the potential spectral density (PSD)vs.frequency in logarithmic scale. The decrease of the PSD slopes, exponentbvalues, indicated a release of spontaneous energy with the advance of pits formation on the stainless steel surface. The data showed that in the range of low frequencies the process that occurs on both stainless steels surfaces could be considered as fractional Brownian motion, an anti-persistent non-stationary process, while in the range of higher frequencies as fractional Gaussian noise, an persistent stationary.

Author(s):  
Vishnu R. ◽  
Jiten Das ◽  
S. B. Arya ◽  
Manish Roy

Recently, ZrN has been attracting interest for its excellent corrosion resistance, biocompatibility, high hardness, good lubricity and ductility. Although tribological study of ZrN coating has been carried out extensively, investigation related to corrosion of ZrN film is limited. In view of this and in view of possible applications of ZrN film in several engineering components, the present investigation has been undertaken to evaluate the corrosion response of ZrN film in seawater solution, Hank's solution, 0.5M H2SO4solution and 0.5M HCl solutions. Towards that purpose, potentiostatic, open circuit potential and potentiodynamic study of ZrN film deposited on plain carbon steel has been carried out in all these solutions. Results indicate that stable protective film is formed on the surface of ZrN coating in all these solution except 0.5M H2SO4 solution. The formation of protective film on ZrN coating is fastest in sea water solution and it is slowest in the Cl¯ ions containing media, 0.5 M HCl. The corrosion current is highest for 0.5M H2SO4 acid solution and least for Hank's solution.


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