ESCA-studies of the structure and composition of the passive film formed on stainless steels by various immersion times in 0.1 M NaCl solution

1987 ◽  
Vol 42 (2) ◽  
pp. 149-165 ◽  
Author(s):  
S. Jin ◽  
A. Atrens
2012 ◽  
Vol 727-728 ◽  
pp. 85-89
Author(s):  
Luzinete P. Barbosa ◽  
Elki C. Souza ◽  
Lucio Salgado ◽  
I. Costa

In this work, the effect of sintering atmosphere on the corrosion resistance of sintered titanium has been evaluated in 0.9 % aqueous NaCl solution to simulate physiological environment. Corrosion tests were performed on titanium porous sintered under vacuum and vacuum plus dynamic argon. The results showed better passive properties associated to the titanium sintered under argon plus vacuum atmosphere than to the vacuum sintered titanium. The better corrosion resistance of the argon plus vacuum sintered titanium was attributed to the formation of a thin passive film on the titanium surface during sintering due the low oxygen content present in this atmosphere.


2017 ◽  
Vol 11 (2) ◽  
pp. 91-95 ◽  
Author(s):  
Eliza Romańczuk ◽  
Zbigniew Oksiuta

AbstractIn this work two austenitic stainless steels, REX734 and 316LV were tested in terms of their microstructure and corrosion properties. The REX734 is a newer generation stainless steel, with modified chemical composition, in comparison to the 316LV grade. Potentiodynamic study of corrosion resistance was conducted in physiological saline solution (0.9% NaCl solution). In spite of the similarities of microstructure, grain size and phase structure in both materials, the corrosion tests revealed that the REX734, with lower nickel and higher nitrogen content, had better corrosion resistance than 316LV. Repassivation potential in the REX734 was almost six times higher than for the 316LV steel. Superior corrosion resistance of the REX734 steel was also confirmed by surface observations of both materials, since bigger and more densely distributed pits were detected in 316LV alloy.


CORROSION ◽  
1993 ◽  
Vol 49 (11) ◽  
pp. 877-884 ◽  
Author(s):  
D. Li ◽  
X. Mao ◽  
R. Zhu

Abstract Kinetics of passive film formation on the bare surface of scratched stainless steels SS in magnesium chloride (MgCl2) solutions were studied using the rapid scratching technique under potentiostatic conditions. An experimental device was designed to record data at the rate of 20,000 points/s, with the rotating rate of the specimen at 3,000 rpm and a scratch scar length of about 4.6 mm to 4.8 mm. A new phenomenon was observed in that two peaks were seen rather than a continuous decay in the curve of current decay on scratched SS in MgCl2 solutions. Current decayed steeply to approximately passive current within about 2.5 ms to 3 ms after the diamond knife was moved away from the specimen. Current rose again for about 2 ms to 3 ms. This phenomenon was considered to represent the processes of adsorbed layer formation on the bare surface and transformation of the adsorbed layer into a passive film. Results were affected by the recording rate of experimental data, the specimen rotating rate, and the scratch scar length. The kinetics of passive film growth were shown empirically by i(t) = I0exp(−βt) with I0 and β being constants. Passive film growth was controlled by ion conduction in a strong electric field, as defined by i = A exp(BV/x).


2007 ◽  
Vol 364-366 ◽  
pp. 215-220
Author(s):  
Shuo Jen Lee ◽  
J.J. Lai ◽  
Yu Ming Lee ◽  
Ming Der Ger ◽  
S.W. Cheng

Passive film of stainless steels possesses good corrosion resistant property. However, the passive film formed in nature is not uniform and the quality is not consistent. It is the major causes for local corrosion. The pitting potential test is a traditional method to test local corrosion of stainless steels. The local corrosion is usually induced by the break-down of the passive film. Therefore, it can be utilized to evaluate the quality of the passive film. Also, because the pitting test is quick and inexpensive, many tests can be performed to evaluate the uniformity of the passive film. This study focuses on SS316 stainless steel. The specimens were treated with electropolishing processes. The original and the processed specimens were tested by pitting potential tests. From these results, the distribution and the uniformity of passive film could be evaluated. An efficient and inexpensive index of the uniformity of the passive film is proposed.


2016 ◽  
Vol 171 ◽  
pp. 239-246 ◽  
Author(s):  
Babatunde Abiodun Obadele ◽  
Anthony Andrews ◽  
Mxolisi Brendon Shongwe ◽  
Peter Apata Olubambi

2011 ◽  
Vol 299-300 ◽  
pp. 427-431
Author(s):  
Yun Li ◽  
Shi Zhi Shang ◽  
Ming Cheng ◽  
Liang Xu ◽  
Shi Hong Zhang

The corrosion behavior of Zr53.5Cu26.5Ni5Al12Ag3 bulk amorphous alloy in 3.5% NaCl solution was investigated by using potentiodynamic polarization experiments and electrochemical impedance spectroscopy (EIS). The results show that Zr53.5Cu26.5Ni5Al12Ag3 bulk amorphous alloy has the better corrosion resistance than its corresponding crystal alloy. During the bath in the 3.5% NaCl solution at 25°C, Zr53.5Cu26.5Ni5Al12Ag3 alloy has the lower corrosion current density than the corresponding crystal alloy. After 100h, the corrosion current densities of Zr53.5Cu26.5Ni5Al12Ag3 and the corresponding crystal alloy are 3.8415×10-8A/cm2 and 5.2827×10-7A/cm2, respectively. The results of EIS test indicate that Zr53.5Cu26.5Ni5Al12Ag3 bulk amorphous alloy has the excellent corrosion resistance because passive film with stable structure formed on the surface in 3.5% NaCl solution. With an increase in the immersion time, the passive film becomes thicker. It leads to impedance resistance and corrosion resistance decrease. The surface of Zr53.5Cu26.5Ni5Al12Ag3 bulk amorphous alloy in 3.5% NaCl solution for 100h was analyzed by SEM and EDS. The results show that the corrosive pitting can be found at both the amorphous alloy and the corresponding crystal alloy. However, the amorphous alloy has the better corrosive pitting resistance than the crystal one because the corrosion products formed by selective dissolving of Zr and Al elements. Moreover, the addition of Ag element helps to improve the corrosion resistance of the amorphous alloy greatly.


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