scholarly journals Electrochemical Behavior of Conventional and Rheo-High-Pressure Die Cast Low Silicon Aluminum Alloys in NaCl Solutions

CORROSION ◽  
10.5006/3254 ◽  
2019 ◽  
Vol 75 (11) ◽  
pp. 1339-1353
Author(s):  
Maryam Eslami ◽  
Flavio Deflorian ◽  
Caterina Zanella

The electrochemical behavior of a low silicon aluminum alloy cast by the conventional and rheo-high-pressure die cast processes is evaluated using polarization test and electrochemical impedance spectroscopy in 0.01 M, 0.05 M, 0.1 M, and 0.6 M sodium chloride solutions. Compared to the conventional high-pressure die cast process, rheocasting introduces some alterations in the microstructure including the presence of aluminum grains with different sizes, formed at different solidification stages. According to the results of the anodic polarization test, conventional cast and rheocast samples show similar breakdown potentials. However, the rheocast samples present enhanced oxygen reduction kinetics compared to the conventional cast sample. Based on scanning electron microscopy examinations, localized microgalvanic corrosion is the main corrosion mechanism for both alloys and it initiates at the interface of aluminum with iron-rich intermetallic particles which are located inside the eutectic regions. The corrosion further develops into the eutectic area. Although the rate of the cathodic reaction can be influenced by the semisolid microstructure, according to the results of anodic polarization and electrochemical impedance spectroscopy tests, the corrosion behavior is not meaningfully affected by the casting process.

2019 ◽  
Vol 306 ◽  
pp. 61-70 ◽  
Author(s):  
Maurilio Pereira Gomes ◽  
Isolda Costa ◽  
Nadine Pébère ◽  
Jesualdo Luiz Rossi ◽  
Bernard Tribollet ◽  
...  

2013 ◽  
Vol 32 (5) ◽  
pp. 493-501
Author(s):  
S.N. Liu ◽  
W. Su ◽  
W.Y. Lu ◽  
Z.F. Wei ◽  
C.L. Zeng

AbstractTo understand the hot corrosion mechanism of materials it is of significance to establish electrochemical measurements under a thin film of fused salts. In this paper, the hot corrosion behavior of Fe-Cr alloys containing 5, 10 and 25wt% Cr, respectively, in the presence of a fused film of 0.9Na2SO4-0.1K2SO4 (mole fraction) at 1173 K in air has been investigated by electrochemical impedance spectroscopy using a two-electrode system. The Nyquist plots for the corrosion of both Fe-5Cr and Fe-10Cr are composed of a very small semicircle at high frequencies and a line at low frequencies indicating that the corrosion is controlled by the diffusion of oxidants in the fused salt film. The alloys were severely corroded, forming a thick porous corrosion layer containing large amounts of non-protective precipitated Fe oxide particles. Conversely, the Nyquist plots for the corrosion of Fe-25Cr are composed of double capacitive loops, with significantly larger impedance values, which are associated with the formation of a protective Cr2O3 scale. Based on the experimental diffusion impedance results and the theoretic solubility and diffusion coefficient of oxygen in molten salts, respectively, a theoretical value of the diffusion flux of molecular O2 has been calculated.


2014 ◽  
Vol 1081 ◽  
pp. 318-321 ◽  
Author(s):  
Dao Bing Huang ◽  
Yuan Qiang Tu ◽  
Ting Hu ◽  
Guang Ling Song ◽  
Xing Peng Guo

The electrochemical behavior of pure Mg in H3PO4 acid (0.42 M) and phosphating solution (0.42 M H3PO4+0.34 M ZnO) was investigated through electrochemical impedance spectroscopy (EIS), potentiodynamic polarization curve and XRD measurements. The results show that Mg has higher corrosion resistance in the phosphating solution than that in the H3PO4 acid which may be due to the relative protective phosphating film on the surface.


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