Pitting Corrosion Behavior of Sintered SUS444 Stainless Steel in MgCl2 Solution

2007 ◽  
Vol 539-543 ◽  
pp. 3255-3260 ◽  
Author(s):  
Satoshi Sunada ◽  
Yusuke Miyazaki ◽  
Kazuhiko Majima
Keyword(s):  
Aqueous Solution ◽  
Stainless Steel ◽  
Corrosion Behavior ◽  
Pitting Corrosion ◽  
Stainless Steels ◽  
Corrosion Potential ◽  
Corrosion Morphology ◽  
Sem Observation ◽  
Porosity Ratio

The pitting corrosion behavior of sintered SUS 444 stainless steels (P/M specimens) with different kinds of porosity ratios of 13.3, 9.11 and 6.88 % was studied in an aqueous solution containing MgCl2 compared with a conventionally processed SUS 444 stainless steel(I/M specimen). The pitting corrosion potential decreased almost linearly as porosity ratio increased, and the I/M specimen showed the best resistance against the initiation of pitting corrosion. The pitting corrosion morphology by SEM observation showed that more small pits were observed on the specimen with larger porosity ratio while less number but larger diameter pits were observed on the specimen with smaller porosity ratio, and it was also confirmed that the I/M specimen had the least number but the largest and deepest pits.

scholarly journals Nitriding of 304 Steel by a Nitrogen Plasma: Increasing Corrosion Resistance

1999 ◽  
Vol 23 (1) ◽  
pp. 38-39
Author(s):  
N. Bellakhal ◽  
K. Draou ◽  
J. L. Brisset
Keyword(s):  
Aqueous Solution ◽  
Stainless Steel ◽  
Corrosion Potential ◽  
Steel Sample ◽  
Nitrogen Plasma ◽  
304 Stainless Steel ◽  
Stainless Steel Sample ◽  
Protective Properties ◽  
Inductively Coupled ◽  
Working Parameters

Exposure of a 304 stainless steel sample to an inductively coupled low pressure radio frequency (RF) nitrogen plasma leads to the formation of a nitriding layer. The protective properties of this layer are investigated by electrochemical methods. The corrosion potential of the steel in an aqueous solution depends on the working parameters of the plasma such as the time exposure and the distance between the steel sample and the high voltage (HV) coil of the treatment reactor.

scholarly journals Influence of Molybdenum on Microstructure and Pitting Corrosion Behavior of Solution-Treated Duplex Stainless Steel in a Lithium Chloride Solution

2019 ◽  
Vol 22 (suppl 1) ◽  
Author(s):  
Stephania Cappellari de Rezende ◽  
Isabela Dainezi ◽  
Raíra Chefer Apolinario ◽  
Lucíola Lucena de Sousa ◽  
Neide Aparecida Mariano
Keyword(s):  
Stainless Steel ◽  
Duplex Stainless Steel ◽  
Corrosion Behavior ◽  
Lithium Chloride ◽  
Pitting Corrosion ◽  
Chloride Solution ◽  
Solution Treated ◽  
Lithium Chloride Solution

Corrosion Resistance Evaluation of a Stainless-Steel Brazed Joint in HCl Solution

2021 ◽  
Vol 1016 ◽  
pp. 997-1002
Author(s):  
Hikaru Nagata ◽  
Masa Ono ◽  
Yasuyuki Miyazawa ◽  
Yuji Hayashi ◽  
Yoshio Bizen
Keyword(s):  
Aqueous Solution ◽  
Stainless Steel ◽  
Corrosion Resistance ◽  
Base Metal ◽  
Corrosion Behavior ◽  
Anodic Polarization ◽  
Filler Metal ◽  
Brazed Joint ◽  
In Situ Observations

To clarify the effect of the acid solution type on corrosion resistance, the corrosion behavior of stainless steel brazed joints in HCl aqueous solution was evaluated through electrochemical measurements. Anodic polarization curves of a ferritic stainless-steel base metal, Ni-based brazing filler metals, and a brazed joint were recorded. In addition, in situ observations were conducted to observe the corrosion behavior of each structure of the brazed joint. Corrosion potentials of the brazing filler metal were lower than that of the base metal. In situ observations of the brazed joint revealed the order of corrosion in aqueous hydrochloric acid. According to the electrochemical measurements, under an actual corrosive environment, the brazing filler metal can function as an anode and selectively corrode. In addition, the anodic polarization curve of the brazed joint showed values between those of the polarization curves of the brazing filler metal and the base metal, indicating that the corrosion resistance could be electrochemically evaluated in HCl aqueous solution.

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