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Corrosion | 2008

Crevice Corrosion Resistance of Alloy 22 in High-Nitrate, High-Temperature Dust Deliquescence Environments

Tiangan Lian; Gregory E. Gdowski; P. D. Hailey; Raul B. Rebak

Abstract Alloy 22 (UNS N06022) has been selected as the corrosion-resistant barrier for the nuclear waste containers in the proposed repository at Yucca Mountain. Alloy 22 may be susceptible to crevice corrosion in the presence of hot chloride-containing solutions. The nitrate ion (NO3−) is an inhibitor for crevice corrosion of Alloy 22 in chloride (Cl−)-containing aqueous solutions. The higher the ratio, R = [NO3−]/[Cl−], is in the solution, the stronger the inhibition of crevice corrosion by nitrate. Atmospheric desert dust contains both chloride and nitrate salts, generally based on sodium (Na+) and potassium (K+). Some of these salts may deliquesce at relatively low humidity at temperatures on the order of 150°C. The resulting deliquesced brines are highly concentrated and especially rich in nitrate (Ratios R ≫ 1). Electrochemical tests have been performed to explore the anodic behavior of Alloy 22 in high-chloride and high-nitrate electrolytes at temperatures as high as 150°C at ambient pressure. Tes...


210th ECS Meeting | 2007

Corrosion Resistances of Iron-Based Amorphous Metals with Yttrium and Tungsten Additions in Hot Calcium Chloride Brine & Natural Seawater: Fe48Mo14Cr15Y2C15B6 and W-Containing Variants

Joseph C. Farmer; J. J. Haslam; S D Day; Tiangan Lian; Cheng K. Saw; Phillip D. Hailey; Jor-Shan Choi; Nancy Y. C. Yang; Craig A. Blue; William H. Peter; Joe H. Payer; D. J. Branagan

Yttrium-containing SAM1651 (Fe{sub 48.0}Cr{sub 15.0}Mo{sub 14.0}B{sub 6.0}C{sub 15.0}Y{sub 2.0}), has a critical cooling rate (CCR) of approximately 80 Kelvin per second, while SAM2X5 (Fe{sub 49.7}Cr{sub 17.7}Mn{sub 1.9}Mo{sub 7.4}W{sub 1.6}B{sub 15.2}C{sub 3.8}Si{sub 2.4}) with no yttrium has a higher critical cooling rate of approximately 600 Kelvin per second. SAM1651s low CCR enables it to be rendered as a completely amorphous material in practical materials processes. Chromium (Cr), molybdenum (Mo) and tungsten (W) provide corrosion resistance; boron (B) enables glass formation; and rare earths such as yttrium (Y) lower critical cooling rate (CCR). The passive film stability of these Fe-based amorphous metal formulations have been found to be superior to that of conventional stainless steels, and comparable to that of Ni-based alloys, based on electrochemical measurements of the passive film breakdown potential and general corrosion rates.


Nuclear Technology | 2008

Corrosion Resistance of Amorphous Fe49.7Cr17.7Mn1.9Mo7.4W1.6B15.2C3.8Si2.4 Coating: A New Criticality Control Material

Joseph C. Farmer; Jor-Shan Choi; Cheng K. Saw; R. H. Rebak; S D Day; Tiangan Lian; Phillip D. Hailey; Joe H. Payer; D. J. Branagan; Louis F. Aprigliano

An iron-based amorphous metal with good corrosion resistance and a high absorption cross section for thermal neutrons has been developed and is reported here. This amorphous alloy has the approximate formula Fe49.7Cr17.7Mn1.9Mo7.4W1.6B15.2C3.8Si2.4 and is known as SAM2X5. Chromium, molybdenum, and tungsten were added to provide corrosion resistance, while boron was added to promote glass formation and the absorption of thermal neutrons. Since this amorphous metal has a higher boron content than conventional borated stainless steels, it provides the nuclear engineer with design advantages for criticality control structures with enhanced safety. While melt-spun ribbons with limited practical applications were initially produced, large quantities (several tons) of gas-atomized powder have now been produced on an industrial scale, and applied as thermal-spray coatings on prototypical half-scale spent-nuclear-fuel containers and neutron-absorbing baskets. These prototypes and other SAM2X5 samples have undergone a variety of corrosion testing, including both salt-fog and long-term immersion testing. Modes and rates of corrosion have been determined in various relevant environments and are reported here. While these coatings have less corrosion resistance than melt-spun ribbons and optimized coatings produced in the laboratory, substantial corrosion resistance has been achieved.


ASME 2006 Pressure Vessels and Piping/ICPVT-11 Conference | 2006

Corrosion Resistance of Iron-Based Amorphous Metal Coatings

Joseph C. Farmer; J. J. Haslam; S. D. Day; Tiangan Lian; Raul B. Rebak; Nancy Y. C. Yang; Louis F. Aprigliano

New amorphous-metal thermal-spray coatings have been developed recently that may provide a viable coating option for spent nuclear fuel & high-level waste repositories [Pang et al. 2002; Shinimiya et al. 2005; Ponnambalam et al. 2004; Branagan et al. 2000–2004]. Some Fe-based amorphous-metal formulations have been found to have corrosion resistance comparable to that of high-performance alloys such as Ni-based Alloy C-22 [Farmer et al. 2004–2006]. These materials rely on Cr, Mo and W for enhanced corrosion resistance, while B is added to promote glass formation and Y is added to lower the critical cooling rate (CCR). Materials discussed in this paper include yttrium-containing SAM1651 with CCR ∼ 80 K/s and yttrium-free Formula 2C with CCR ∼ 600 K/s. While nickel-based Alloy C-22 and Type 316L stainless steel lose their resistance to corrosion during thermal spraying, Fe-based SAM1651 and Formula 2C amorphous-metal coatings can be applied with thermal spray processes without any significant loss of corrosion resistance. In the future, such corrosion-resistant thermal-spray coatings may enable the development of less expensive containers for spent nuclear fuel (SNF) and high-level waste (HLW), including enhanced multipurpose containers (MPCs), protected closure welds, and shields to protect containers from drips and falling rocks. These materials are extremely hard and provide enhanced resistance to abrasion and gouges from backfill operations. For example, Type 316L stainless steel has a hardness of approximately 150 VHN, Alloy C-22 has a hardness of approximately 250 VHN, while the Fe-based amorphous metals typically have hardness values of 1100–1300 VHN. Both Formula 2C and SAM1651 have high boron content which allow them to absorb neutrons, and therefore be used for enhanced criticality control. Cost savings can also be realized through the substitution of Fe-based alloy for Ni-based materials. Applications are also envisioned in oil & gas industry.© 2006 ASME


Presented at: 2007 ASME Pressure Vessels and Piping Division Conference, San Antonio, TX, United States, Jul 22 - Jul 26, 2007 | 2007

Crevice Repassivation Potential of Alloy 22 in High-Nitrate Dust Deliquescence Type Environments

Tiangan Lian; Gregory E. Gdowski; Phillip D. Hailey; Raul B. Rebak

The nitrate ion (NO{sub 3}{sup -}) is an inhibitor for crevice corrosion of Alloy 22 (N06022) in chloride (Cl{sup -}) aqueous solutions. Naturally formed electrolytes may contain both chloride and nitrate ions. The higher the ratio R = [NO{sub 3}{sup -}]/[Cl{sup -}] in the solution the stronger the inhibition of crevice corrosion. Atmospheric desert dust contains both chloride and nitrate salts, generally based on sodium (Na{sup +}) and potassium (K{sup +}). Some of these salts may deliquescence at relatively low humidity at temperatures on the order of 150 C and higher. The resulting deliquescent brines are highly concentrated and especially rich in nitrate. Electrochemical tests have been performed to explore the anodic behavior of Alloy 22 in high chloride high nitrate electrolytes at temperatures as high as 150 C at ambient atmospheres. Naturally formed brines at temperatures higher than 120 C do not induce crevice corrosion in Alloy 22 because they contain high levels of nitrate. The inhibitive effect of nitrate on crevice corrosion is still active for temperatures higher than 100 C.


Presented at: 2007 ASME Pressure Vessels and Piping Division Conference, San Antonio, TX, United States, Jul 22 - Jul 26, 2007 | 2007

Enhanced Corrosion Resistance of Iron-Based Amorphous Alloys

Raul B. Rebak; S. Daniel Day; Tiangan Lian; Louis F. Aprigliano; Phillip D. Hailey; Joseph C. Farmer

Iron-based amorphous alloys possess enhanced hardness and are highly resistant to corrosion, which make them desirable for wear applications in corrosive environments. It was of interest to examine the behavior of amorphous alloys during anodic polarization in concentrated salt solutions and in the salt-fog testing. Results from the testing of one amorphous material (SAM2X5) both in ribbon form and as an applied coating are reported here. Cyclic polarization tests were performed on SAM2X5 ribbon as well as on other nuclear engineering materials. SAM2X5 showed the highest resistance to localized corrosion in 5 M CaCl{sub 2} solution at 105 C. Salt fog tests of 316L SS and Alloy 22 coupons coated with amorphous SAM2X5 powder showed resistance to rusting. Partial devitrification may be responsible for isolated pinpoint rust spots in some coatings.


Journal of Materials Research | 2006

A High-Performance Corrosion-Resistant Iron-Based Amorphous Metal - The Effects of Composition, Structure and Environment on Corrosion Resistance

Joseph C. Farmer; J. J. Haslam; Dan Day; Tiangan Lian; Cheng K. Saw; Phillip D. Hailey; J-S. Choi; Raul B. Rebak; Nancy Y. C. Yang; Robert Bayles; Louis F. Aprigliano; Joe H. Payer; J.H. Perepezko; K. Hildal; Enrique J. Lavernia; Leo Ajdelsztajn; D. J. Branagan; Brad Beardsley

New corrosion-resistant, iron-based amorphous metals have been identified from published data or developed through combinatorial synthesis, and tested to determine their relative thermal phase stability, microstructure, mechanical properties, damage tolerance, and corrosion resistance. Some alloy additions are known to promote glass formation and to lower the critical cooling rate [F. Guo, S. J. Poon, Applied Physics Letters, 83 (13) 2575-2577, 2003]. Other elements are known to enhance the corrosion resistance of conventional stainless steels and nickel-based alloys [A. I. Asphahani, Materials Performance, Vol. 19, No. 12, pp. 33-43, 1980] and have been found to provide similar benefits to iron-based amorphous metals. Many of these materials can be cast as relatively thick ingots, or applied as coatings with advanced thermal spray technology. A wide variety of thermal spray processes have been developed by industry, and can be used to apply these new materials as coatings. Any of these can be used for the deposition of the formulations discussed here, with varying degrees of residual porosity and crystalline structure. Thick protective coatings have now been made that are fully dense and completely amorphous in the as-sprayed condition. An overview of the High-Performance Corrosion Resistant Materials (HPCRM) Project will be given, with particular emphasis on the corrosion resistance of several different types of iron-based amorphous metals in various environments of interest. The salt fog test has been used to compare the performance of various wrought alloys, melt-spun ribbons, arc-melted drop-cast ingots, and thermal-spray coatings for their susceptibility to corrosion in marine environments. Electrochemical tests have also been performed in seawater. Spontaneous breakdown of the passive film and localized corrosion require that the open-circuit corrosion potential exceed the critical potential. The resistance to localized corrosion is seawater has been quantified through measurement of the open-circuit corrosion potential (E{sub corr}), the breakdown potential (E{sub crit}) and the repassivation potential (E{sub rp}). The greater the difference between the open-circuit corrosion potential and the repassivation potential ({Delta}E), the more resistant a material is to modes of localized corrosion such as pitting and crevice corrosion. Cyclic polarization (CP) was used as a means of measuring the critical potential (E{sub crit}) relative to the open-circuit corrosion potential (E{sub corr}). Linear polarization (LP) has been used to determine the corrosion current (i{sub corr}) and the corresponding corrosion rate. Other aspects of the materials will also be discussed, as well as potential applications.


Corrosion | 2002

Effect of Thermal Aging on the Corrosion Behavior of Wrought and Welded Alloy 22

Raul B. Rebak; T.S. Edgecumbe; Tiangan Lian; R.M. Carranza; Jeffrey R. Dillman; T. Corbin; Paul Crook

Alloy 22 (UNS N06022) is a candidate material for the external wall of the high level nuclear waste containers for the potential repository site at Yucca Mountain. In the mill-annealed (MA) condition, Alloy 22 is a single face centered cubic phase. When exposed to temperatures on the order of 600 C and above for times higher than 1 h, this alloy may develop secondary phases that are brittle and offer a lower corrosion resistance than the MA condition. The objective of this work was to age Alloy 22 at temperatures between 482 C and 800 C for times between 0.25 h and 3,000 h and to study the corrosion performance of the resulting material. Aging was carried out using wrought specimens as well as gas tungsten arc welded (GTAW) specimens. The corrosion performance was characterized using standard immersion tests in aggressive acidic solutions and electrochemical tests in multi-component solutions. Results show that, in general, in aggressive acidic solutions the corrosion rate increased as the aging temperature and aging time increased. However, in multi ionic environments that could be relevant to the potential Yucca Mountain site, the corrosion rate of aged material was the same as the corrosion rate of the MA material.


MRS Proceedings | 1999

A Quantitative Assessment of Microbiological Contributions to Corrosion of Candidate Nuclear Waste Package Materials

Tiangan Lian; S. Martin; J. Horn; D. Jones

The U.S. Department of Energy is contributing to the design of a potential nuclear-waste repository at Yucca Mountain, Nevada. A system to predict the contribution of Yucca Mountain (YM) bacteria to overall corrosion rates of candidate waste-package (WP) materials was designed and implemented. DC linear polarization resistance techniques were applied to candidate material coupons that had been inoculated with a mixture of YM-derived bacteria with potentially corrosive activities or left sterile. Inoculated bacteria caused a 5- to 6-fold increase in corrosion rate of carbon steel C1020 (to approximately 7Ð8mm/yr) and an almost 100-fold increase in corrosion rate of Alloy 400 (to approximately 1mm/yr). Microbiologically influenced corrosion (MIC) rates on more resistant materials (CRMs: Alloy 625, Type 304 Stainless Steel, and Alloy C22) were on the order of hundredths of micrometers per year (mm/yr). Bulk chemical and surfacial end-point analyses of spent media and coupon surfaces showed preferential dissolution of nickel from Alloy 400 coupons and depletion of chromium from CRMs after incubation with YM bacteria. Scanning electron microscopy (SEM) also showed greater damage to the Alloy 400 surface than that indicated by electrochemical detection methods.


MRS Proceedings | 2006

Comparative Study on the Corrosion Resistance of Fe-Based Amorphous Metal, Borated Stainless Steel and Ni-Cr-Mo-Gd Alloy

Tiangan Lian; Daniel Day; Phillip D. Hailey; Jor-Shan Choi; Joseph C. Farmer

Iron-based amorphous alloy Fe{sub 49.7}Cr{sub 17.7}Mn{sub 1.9}Mo{sub 7.4}W{sub 1.6}B{sub 15.2}C{sub 3.8}Si{sub 2.4} was compared to borated stainless steel and Ni-Cr-Mo-Gd alloy on their corrosion resistance in various high-concentration chloride solutions. The melt-spun ribbon of this iron-based amorphous alloy have demonstrated a better corrosion resistance than the bulk borated stainless steel and the bulk Ni-Cr-Mo-Gd alloy, in high-concentration chloride brines at temperatures 90 deg. C or higher. (authors)

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Joseph C. Farmer

Lawrence Livermore National Laboratory

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Raul B. Rebak

Lawrence Livermore National Laboratory

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Phillip D. Hailey

Lawrence Livermore National Laboratory

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J. J. Haslam

Lawrence Livermore National Laboratory

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Joe H. Payer

Case Western Reserve University

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Jor-Shan Choi

Lawrence Livermore National Laboratory

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Cheng K. Saw

Lawrence Livermore National Laboratory

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Louis F. Aprigliano

Oak Ridge National Laboratory

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Nancy Y. C. Yang

Sandia National Laboratories

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S D Day

Sandia National Laboratories

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