Effect of Thiosulfate on Pitting Corrosion of Ni-Cr-Fe Alloys in Chloride Solutions

Pitting corrosion of Alloys 600, 690, and 800 (UNS N06600, N06690, and N08800) was studied in 1 M NaCl solution with different concentrations of thiosulfate (). Alloys exhibited vastly different electrochemical behavior, depending on the concentration and chromium content of the alloy. Alloy 600 exhibited a breakdown and repassivation potential that decreased with decreasing concentration, in the range from 1 M to 10−4 M. Breakdown and repassivation potentials decreased about 300 mV and 600 mV, respectively, when 10−4 M was added to a 1 M NaCl solution. For Alloys 690 and 800, additions of in the range of 1 M to 0.01 M caused a decrease in the breakdown and repassivation potentials. Dilute solutions were more aggressive, and a 0.01 M addition of to a 1 M NaCl solution caused a decrease in breakdown and repassivation potentials of about 300 mV. In a solution containing 0.001 M Na2S2O3 + 1 M NaCl, Alloys 690 and 800 showed two different submodes of pitting, each one of them existing at a different range of potential. Chloride pitting corrosion was observed at high potentials and was characterized by pits with a lacy cover. The stable pit initiation potential associated with this process in both alloys was near 300 mVAg/AgCl and was preceded by frequent metastable events. Chloride plus pitting was observed at low potentials (near −225 mVAg/AgCl) and was characterized by hemispherical pits. In potentiodynamic curves, this submode of pitting showed a characteristic anodic peak of approximately 120 mV width and a maximum current density of 10 μA/cm2 for both alloys. Potentiostatic tests at potentials within this anodic peak led to stable pit growth. Those pits could be repassivated by scanning the potential either in noble or active directions. Low-potential and high-potential pitting submodes were separated by a stable passivity range, as determined by potentiodynamic curves. Upon a further decrease in concentration down to 10−4 M, only high-potential pitting corrosion was observed, with pitting and repassivation potentials similar than those in 1 M NaCl solution.

Effects of Alloying Elements on the Corrosion Behavior of Sputter–deposited Zr–(12–21)Cr–W Alloys in 0.5 M NaCl Solution

The synergistic effect of the simultaneous additions of tungsten and zirconium in thesputter-deposited amorphous or nanocrystalline Zr-(12-21)Cr-W alloys is studied in 0.5 MNaCl solution open to air at 25°C using corrosion tests and open circuit potentialmeasurements. Corrosion rates of the sputter-deposited Zr-(12-21)Cr-W alloys containing10-80 at % tungsten (that is, 0.95-1.85 x 10-2 mm.y-1) are more than one order of magnitudelower than that of the sputter-deposited tungsten and even lower than those of zirconium aswell as chromium in 0.5 M NaCl solution. The addition of 8-73 at % zirconium content inthe sputter-deposited binary W-(12-21)Cr alloys seems to be more effective to improve thecorrosion-resistant properties of the sputter-deposited ternary Zr-Cr-W alloys containing12-21 at % chromium in 0.5 M NaCl solution. The sputter-deposited Zr-(17-21)Cr-W alloyscontaining an adequate amounts of zirconium metal showed the more stable passivity andshowed higher corrosion resistance than those of alloy-constituting elements in 0.5 M NaClsolution open to air at 25°C.Keywords: Zr-(12-21)Cr-W alloys, sputter deposition, corrosion test, open circuit potential,0.5 M NaCl.DOI: 10.3126/jncs.v25i0.3305Journal of Nepal Chemical Society Volume 25, 2010 pp 75-82