TY - GEN
T1 - Electrochemical behavior of Al 356 metallic foams in choride media
AU - Vásquez, M.
AU - Calderón, J. A.
AU - Fernández, P.
PY - 2011
Y1 - 2011
N2 - Aluminium metallic foams are part of a new family of materials called cellular metals CM, which have a porous structure that give them an excellent combination of physical, chemical and mechanical properties. In our work we used the 356 Al alloy for the manufacture of metallic foams from NaCl Soluble Preform Infiltration method. Despite the potential application of these foams, their performance may be affected by corrosion caused by salt remnant that could be inside of the foams due to poor washing practices. To study the electrochemical behavior of the 356 Al alloy in NaCl, polarization curves and electrochemical impedance spectroscopy were performed in rotating disk electrode RDE, and in porous rotating disk electrode PRDE made from aluminium foams. The results showed that cathodic reaction of oxygen reduction is the crucial stage of the process of dissolution of the material for both electrodes. In the corrosion process there is also an effect of oxygen transport, which limits the overall process of corrosion of the material. In addition it was found that due to the large surface area of the foams, the cathodic limiting current is much greater than for a solid electrode, thereby obtaining a dissimilar behavior to that described by Levich. The behavior of the porous electrode was quite similar to that found by Bomi Nam and coworkers in their work, where the limiting current reaches a highest value at very high electrode rotation speed. Nyquist plots were performed at -20 mV vs OCP to avoid the scatter in the curves that is typical in curves obtain at OCP values. The pitting potential of the aluminium at these conditions coincides with the corrosion potential, making impossible the system to get stable.
AB - Aluminium metallic foams are part of a new family of materials called cellular metals CM, which have a porous structure that give them an excellent combination of physical, chemical and mechanical properties. In our work we used the 356 Al alloy for the manufacture of metallic foams from NaCl Soluble Preform Infiltration method. Despite the potential application of these foams, their performance may be affected by corrosion caused by salt remnant that could be inside of the foams due to poor washing practices. To study the electrochemical behavior of the 356 Al alloy in NaCl, polarization curves and electrochemical impedance spectroscopy were performed in rotating disk electrode RDE, and in porous rotating disk electrode PRDE made from aluminium foams. The results showed that cathodic reaction of oxygen reduction is the crucial stage of the process of dissolution of the material for both electrodes. In the corrosion process there is also an effect of oxygen transport, which limits the overall process of corrosion of the material. In addition it was found that due to the large surface area of the foams, the cathodic limiting current is much greater than for a solid electrode, thereby obtaining a dissimilar behavior to that described by Levich. The behavior of the porous electrode was quite similar to that found by Bomi Nam and coworkers in their work, where the limiting current reaches a highest value at very high electrode rotation speed. Nyquist plots were performed at -20 mV vs OCP to avoid the scatter in the curves that is typical in curves obtain at OCP values. The pitting potential of the aluminium at these conditions coincides with the corrosion potential, making impossible the system to get stable.
KW - Al foams
KW - Cellular Metals
KW - Electrochemical techniques
KW - PRDE
KW - RDE
KW - Soluble Preform Infiltration
UR - http://www.scopus.com/inward/record.url?scp=84867242234&partnerID=8YFLogxK
M3 - Ponencia publicada en las memorias del evento con ISBN
AN - SCOPUS:84867242234
SN - 9781618393630
T3 - 18th International Corrosion Congress 2011
SP - 936
EP - 942
BT - 18th International Corrosion Congress 2011
T2 - 18th International Corrosion Congress 2011
Y2 - 20 November 2011 through 24 November 2011
ER -