Environmental Effects on Localized Corrosion of a High-Level Nuclear Waste Container Material

1990 ◽  
Vol 212 ◽  
Author(s):  
N. Sridhar ◽  
G. Cragnolino ◽  
W. Machowski

ABSTRACTThe effect of environmental variables on the localized corrosion behavior of alloy 825 is examined in this paper. Cyclic, potentiodynamic polarization tests based on a two-level, full factorial experimental design were conducted. An index incorporating both the visual and scanning electron microscope examinations of localized corrosion and the electrochemical parameters was used for the statistical analysis. The analysis showed that chloride is the single most important promoter of localized corrosion, while nitrate was the single most important inhibitor. Fluoride was a weak inhibitor, especially at low chloride levels. Sulfate was a weak promoter, especially at high chloride levels. Temperature did not have a significant effect within the chloride levels examined. Separate experiments indicated that silicon, added as metasilicate, did not have any significant effect on localized corrosion. The adverse effect of chloride was observed at concentrations as low as 100 ppm. Addition of H2O2 increased the corrosion potential of alloy 825 to a value above the repassivation potential observed in the 300 ppm chloride solution.

1994 ◽  
Vol 353 ◽  
Author(s):  
Narasi Sridhar ◽  
Darrell Dunn ◽  
Gustavo Cragnolino

AbstractLocalized corrosion in aqueous environments forms an important bounding condition for the performance assessment of high-level waste (HLW) container materials. A predictive methodology using repassivation potential is examined in this paper. It is shown, based on long-term (continuing for over 11 months) testing of alloy 825, that repassivation potential of deep pits or crevices is a conservative and robust parameter for the prediction of localized corrosion. In contrast, initiation potentials measured by short-term tests are non-conservative and highly sensitive to several surface and environmental factors. Corrosion data from various field tests and plant equipment performance are analyzed in terms of the applicability of repassivation potential. The applicability of repassivation potential for predicting the occurrence of stress corrosion cracking (SCC) and intergranular corrosion in chloride containing environments is also examined.


2010 ◽  
Vol 1265 ◽  
Author(s):  
Mauricio Rincon Ortiz ◽  
Martín A. Rodríguez ◽  
Ricardo M. Carranza ◽  
Raul B. Rebak

AbstractAlloy 22 belongs to the Ni-Cr-Mo family and it is highly resistant to general and localized corrosion. It may suffer crevice corrosion in aggressive environmental conditions. This alloy has been considered as a corrosion-resistant barrier for high-level nuclear waste containers. It is assumed that localized corrosion may occurs when the corrosion potential (ECORR) is equal or higher than the crevice corrosion repassivation potential (ER,CREV). The latter is measured by means of different electrochemical techniques using artificially creviced specimens. These techniques include cyclic potentiodynamic polarization (CPP) curves, Tsujikawa-Hisamatsu electrochemical (THE) method or other non-standard methods, such as the PD-GS-PD technique.The aim of the present work was to determine reliable critical or protection potentials for crevice corrosion of Alloy 22 in pure chloride solutions at 90°C. Conservative methodologies (which include extended potentiostatic steps) were applied for determining protection potentials below which crevice corrosion cannot initiate and propagate. Results from PD-GS-PD technique were compared with those from these methodologies in order to assess their reliability. Results from the CPP and the THE methods were also considered for comparison. The repassivation potential resulting from the PD-GS-PD technique was conservative and reproducible, and it did not depend on the amount of previous crevice corrosion propagation.


1993 ◽  
Vol 333 ◽  
Author(s):  
John C. Walton ◽  
Narasi Sridhar ◽  
Gustavo Cragnolino ◽  
Tony Torng ◽  
Prasad Nair

ABSTRACTOne of the requirements for the performance of waste packages prescribed in 10CFR 60.113 is that the high level waste must be “substantially completely” contained for a minimum period of 300 to 1000 years. During this period, the radiation and thermal conditions in the engineered barrier system and the near-field environment are dominated by fission product decay. In the present U.S design of the engineered barrier system, the outer container plays a dominant role in maintaining radionuclide containment. A quantitative methodology for analyzing the performance of the container is described in this paper. This methodology enables prediction of the evolution of the waste package environment in terms of temperature fields, stability of liquid water on the container surface, and concentration of aggressive ions such as chloride. The initiation and propagation of localized corrosion is determined by the corrosion potential of the container material and critical potentials for localized corrosion. The coiTOsion potential is estimated from the kinetics of the anodic and cathodic reactions including oxygen diffusion through scale layers formed on the container surface. The methodology described is applicable to a wide range of metals, alloys and environmental conditions.


1982 ◽  
Vol 15 ◽  
Author(s):  
T. M. Ahn ◽  
B. S. Lee ◽  
J. Woodward ◽  
R. L. Sabatini ◽  
P. Soo

ABSTRACTThe corrosion behavior of TiCode-12 (Ti-0.3 Mo-0.8 Ni) high level nuclear waste container alloy has been studied for a simulated WIPP brine at a temperature of 150°C or below. Crevice corrosion was identified as a potentially important failure mode for this material. Within a mechanical crevice, a thick oxide film was found and shown to be the rutile form of TiO2, with a trace of lower oxide also present. Acidic conditions were found to cause a breakdown of the passive oxide layer. Solution aeration and increased acidity accelerate the corrosion rate. In hydrogen embrittlement studies, it was found that hydrogen causes a significant decrease in the apparent stress intensity level in fracture mechanics samples. Hydride formation is thought to be responsible for crack initiation. Stress corrosion cracking under static loads was not observed. Attention has also been given to methods for extrapolating short term uniform corrosion rate data to extended times.


1999 ◽  
Vol 556 ◽  
Author(s):  
D. S. Dunn ◽  
G. A. Cragnolino ◽  
N. Sridhar

AbstractFor the geologic disposal of the high level nuclear waste (HLW), aqueous corrosion is considered to be the most important factor in the long-term performance of containers, which are the main components of the engineered barrier subsystem. Container life, in turn, is important to the overall performance of the repository system. The proposed container designs and materials have evolved to include multiple barriers and highly corrosion resistant Ni-Cr-Mo alloys, such as Alloys 625 and C-22. Calculations of container life require knowledge of the initiation time and growth rate of localized corrosion. In the absence of localized corrosion, the rate of general or uniform dissolution, given by the passive current density of these materials, is needed. The onset of localized corrosion may be predicted by using the repassivation and corrosion potentials of the candidate container materials in the range of expected repository environments. In initial corrosion tests, chloride was identified as the most detrimental anionic species to the performance of Ni-Cr-Mo alloys. Repassivation potential measurements for Alloys 825, 625, and C-22, conducted over a wide range of chloride concentrations and temperatures, are reported. In addition, steady state passive current density, which will determine the container lifetime in the absence of localized corrosion, was measured for Alloy C-22 under various environmental conditions.


2004 ◽  
Vol 824 ◽  
Author(s):  
Yi-Ming Pan ◽  
Gustavo A. Cragnolino

AbstractA sample of josephinite, a rock containing predominantly a Ni-Fe metallic phase, was evaluated as a natural metal analog to increase confidence in the assessment of waste package performance for the potential high-level radioactive waste repository at Yucca Mountain, Nevada. The josephinite sample was characterized electrochemically in simulated groundwater environments using cyclic potentiodynamic polarization and potentiostatic tests. The passive surface layers formed potentiostatically were examined by X-ray photoelectron spectroscopy. These results were compared to those obtained with a synthetic Ni3Fe alloy with a chemical composition similar to that of josephinite. Electrochemical studies showed that josephinite exhibited passivity at a slightly higher pH than did the cast Ni3Fe alloy and was found to be slightly more susceptible to pitting corrosion. The passive films formed on the josephinite and the cast Ni3Fe alloy have a duplex structure consisting of an Fe-rich hydroxide outer layer and a Ni-rich oxide inner layer. Results obtained from this study provide an appropriate characterization of the environmental conditions leading to the passivity and localized corrosion of josephinite. Extended persistence of a stable passive film, however, is essential for the long-term stability of the josephinite sample. The relationship between the passive behavior and the formation of alteration layers needs to be established for assessing the survivability of josephinite.


Sign in / Sign up

Export Citation Format

Share Document