Electrochemical behavior of carbon steel in alkaline sour environments measured by electrochemical impedance spectroscopy

2000 ◽  
Vol 46 (4) ◽  
pp. 487-497 ◽  
Author(s):  
R Cabrera-Sierra ◽  
I Garcı́a ◽  
E Sosa ◽  
T Oropeza ◽  
I González
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.


2013 ◽  
Vol 652-654 ◽  
pp. 1432-1435
Author(s):  
Qian Hu ◽  
Jing Liu ◽  
Jie Zhang ◽  
Feng Huang ◽  
Xing Peng Guo

The crevice corrosion behaviors of X52 carbon steel in two typical Cl--containing solutions were investigated by electrochemical noise and electrochemical impedance spectroscopy. Results show that oxygen concentration difference leads to the coupled current in NaCl + NaHCO3 solution while HAc concentration difference causes the coupled current in NaCl solution saturated with CO2 in the presence of HAc. There exists an apparent incubation stage during the crevice corrosion process of X52 carbon steel in the former. However, no obvious incubation period of crevice corrosion can be observed in the latter. Micrography shows that the crevice corrosion occurs indeed and the corrosion inside the crevice is not uniform.


2018 ◽  
Vol 4 (1) ◽  
pp. 47-54 ◽  
Author(s):  
Nilesh S. Bagal ◽  
Vaibhav S. Kathavate ◽  
Pravin P. Deshpande

AbstractThe present study aims at deposition of zinc phosphate coatings on low carbon steel with incorporated nano- TiO2 particles by chemical phosphating method. The coated low carbon steel samples were assessed in corrosion studies using electrochemical impedance spectroscopy and potentiodynamic polarization techniques (Tafel) in 3.5% NaCl solution. Morphology and chemical composition of the coatings were analyzed by scanning electron microscopy and energy dispersive X-ray spectroscopy in order to observe growth of coating. Significant variations in the coating weight, porosity and corrosion resistance were observed with the addition of nano- TiO2 in the phosphating bath. Corrosion rate of nano-TiO2 chemical phosphate coated samples was found to be 3.5 milli inches per year which was 3 times less than the normal phosphate-coated sample (8 mpy). Electrochemical impedance spectroscopy studies reveal reduction of porosity of nano-TiO2 phosphate coated samples. It was found that nano-TiO2 particles in the phosphating solution yielded uniform phosphate coatings of higher coating weight, fewer defects and enhanced corrosion resistance than the normal zinc phosphate coatings (developed using normal phosphating bath).


2019 ◽  
Vol 43 (1) ◽  
pp. 71-77 ◽  
Author(s):  
Adriano H. Akita ◽  
Cecílio S. Fugivara ◽  
Idalina V. Aoki ◽  
Assis V. Benedetti

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