Atmospheric Corrosion Behavior of 2A12 Aluminum Alloy in a Tropical Marine Environment

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Zhongyu Cui

2015-01-01

Full Text Available Atmospheric corrosion behavior of 2A12 aluminum alloy exposed to a tropical marine environment for 4 years was investigated. Weight loss of 2A12 alloy in the log-log coordinates can be well fitted with two linear segments, attributing to the evolution of the corrosion products. EIS results indicate that the corrosion product layer formed on the specimens exposed for 12 months or longer presents a good barrier effect. Corrosion morphology changes from pitting corrosion to severe intergranular corrosion with the extension of exposure time, resulting in the reduction of the mechanical properties.

The Moessbauer spectroscopy in the characterization of atmospheric corrosion products

International Nuclear Information System (INIS)

Hernandez Torres, D.; Leiva Ronda, P.; Gomez, J.; Ronda, M.

1996-01-01

A study of corrosion products on mild steel formed after 1 and 5 years exposure in two industrial coastal weathering stations in the Bay from Matanzas City, Cuba, has been carried out. Structural analysis was conducted using mainly transmission Moessbauer Spectroscopy and the X-ray diffraction as complementary technique. The main phases found in the specimen exposed to high chloride containing environment were: lepidocrocite (γ- FeOOH), goethite (α- FeOOH) and magnetite concentration was the lowest, the phases found were γ- FeOOH and α- FeOOH, and the phase transformation proposed was γ- FeOOh -> α- Fe-OOH. In this station were found also amorphous corrosion products. There amorphous phases could be responsible for the lowest levels of corrosion on steel in this station

Timescale Correlation between Marine Atmospheric Exposure and Accelerated Corrosion Testing

Science.gov (United States)

Montgomery, Eliza L.; Calle, Luz Marina; Curran, Jerone C.; Kolody, Mark R.

2011-01-01

Evaluation of metal-based structures has long relied on atmospheric exposure test sites to determine corrosion resistance in marine environments. Traditional accelerated corrosion testing relies on mimicking the exposure conditions, often incorporating salt spray and ultraviolet (UV) radiation, and exposing the metal to continuous or cyclic conditions of the corrosive environment. Their success for correlation to atmospheric exposure is often a concern when determining the timescale to which the accelerated tests can be related. Accelerated laboratory testing, which often focuses on the electrochemical reactions that occur during corrosion conditions, has yet to be universally accepted as a useful tool in predicting the long term service life of a metal despite its ability to rapidly induce corrosion. Although visual and mass loss methods of evaluating corrosion are the standard and their use is imperative, a method that correlates timescales from atmospheric exposure to accelerated testing would be very valuable. This work uses surface chemistry to interpret the chemical changes occurring on low carbon steel during atmospheric and accelerated corrosion conditions with the objective of finding a correlation between its accelerated and long-term corrosion performance. The current results of correlating data from marine atmospheric exposure conditions at the Kennedy Space Center beachside corrosion test site, alternating seawater spray, and immersion in typical electrochemical laboratory conditions, will be presented. Key words: atmospheric exposure, accelerated corrosion testing, alternating seawater spray, marine, correlation, seawater, carbon steel, long-term corrosion performance prediction, X-ray photoelectron spectroscopy.

Understanding corrosion via corrosion product characterization: II. Role of alloying elements in improving the corrosion resistance of Zn-Al-Mg coatings on steel

International Nuclear Information System (INIS)

Volovitch, P.; Vu, T.N.; Allely, C.; Abdel Aal, A.; Ogle, K.

2011-01-01

Highlights: → Origins of better corrosion resistance of ZnAlMg coatings than galvanized steel. → Comparative study of corrosion products formed on ZnAlMg, ZnMg and Zn coatings. → Modeling of dissolution and precipitation stages of corrosion. → At early stages Mg stabilizes protective zinc basic salts during dry-wet cycling. → At later stages Al dissolves at high pH forming protective layered double hydroxides. - Abstract: Corrosion products are identified on Zn, ZnMg and ZnAlMg coatings in cyclic corrosion tests with NaCl or Na 2 SO 4 containing atmospheres. For Mg-containing alloys the improved corrosion resistance is achieved by stabilization of protective simonkolleite and zinc hydroxysulfate. At later stages, the formation of layered double hydroxides (LDH) is observed for ZnAlMg. According to thermodynamic modeling, Mg 2+ ions bind the excess of carbonate or sulfate anions preventing the formation of soluble or less-protective products. A preferential dissolution of Zn and Mg at initial stages of corrosion is confirmed by in situ dissolution measurement. The physicochemical properties of different corrosion products are compared.

The effects of air pollution and climatic factors on atmospheric corrosion of marble under field exposure

International Nuclear Information System (INIS)

Lan, Tran Thi Ngoc; Nishimura, Rokuro; Tsujino, Yoshio; Satoh, Yukihiro; Thi Phuong Thoa, Nguyen; Yokoi, Masayuki; Maeda, Yasuaki

2005-01-01

The atmospheric corrosion of marble was evaluated in terms of SO 2 concentration as air pollution and climatic factors such as rainfall, relative humidity, temperature and so on under the field exposure. Marble of calcite type (CaCO 3 ) was exposed to outdoor atmospheric environment with and without a rain shelter at four test sites in the southern part of Vietnam for 3-month, 1- and 2-year periods from July 2001 to September 2003. The thickness loss of marble was investigated gravimetrically. X-ray diffraction and X-ray fluorescent methods were applied to study corrosion products on marble. The corrosion product of marble was only gypsum (CaSO 4 . 2H 2 O) and was washed out by rain under the unsheltered exposure condition. It was found that the most substantial factors influencing the corrosion of marble were rainfall, SO 2 concentration in the air and relative humidity. Based on the results obtained, we estimated the dose-response functions for the atmospheric corrosion of marble in the southern part of Vietnam

Atmospheric Corrosion Behavior and Mechanism of a Ni-Advanced Weathering Steel in Simulated Tropical Marine Environment

Science.gov (United States)

Wu, Wei; Zeng, Zhongping; Cheng, Xuequn; Li, Xiaogang; Liu, Bo

2017-12-01

Corrosion behavior of Ni-advanced weathering steel, as well as carbon steel and conventional weathering steel, in a simulated tropical marine atmosphere was studied by field exposure and indoor simulation tests. Meanwhile, morphology and composition of corrosion products formed on the exposed steels were surveyed through scanning electron microscopy, energy-dispersive x-ray spectroscopy and x-ray diffraction. Results indicated that the additive Ni in weathering steel played an important role during the corrosion process, which took part in the formation of corrosion products, enriched in the inner rust layer and promoted the transformation from loose γ-FeOOH to dense α-FeOOH. As a result, the main aggressive ion, i.e., Cl-, was effectively separated in the outer rust layer which leads to the lowest corrosion rate among these tested steels. Thus, the resistance of Ni-advanced weathering steel to atmospheric corrosion was significantly improved in a simulated tropical marine environment.

Validation of a chromatographic method and its use in the determination of sulphates in the products of atmospheric corrosion of zinc exposed to SO2 and NO2

International Nuclear Information System (INIS)

Montoya, Paula; Castano, Juan G

2005-01-01

The role of SO 2 and NO 2 in the atmospheric corrosion of zinc was studied by determining sulphates as the main products of corrosion when this metal is exposed to atmospheres containing SO 2 and NO 2 , scanning electron microscopy (SEM/EDX) and Ion Exchange Chromatography (IC) were used as instrumental techniques, the former was used to establish the morphology and the elementary qualitative determination of corrosion products, and the latter to quantify sulphates, before conducting the chromatographic analyses a series of parameters such as selectivity, linearity, precision, accuracy, limit of quantification, and detection limit, were evaluated to validate the method and to have the statistical certainty of its utility in the sulphate quantification, the results showed that when the metal is exposed to an atmosphere containing SO 2 and NO 2 , the sulphate formation increases with exposure time, a synergetic effect of both polluting agents on sulphate formation was found with respect to the sulphate formation in atmospheres containing only SO 2

Atmospheric corrosion of metals in industrial city environment

OpenAIRE

Kusmierek, Elzbieta; Chrzescijanska, Ewa

2015-01-01

Atmospheric corrosion is a significant problem given destruction of various materials, especially metals. The corrosion investigation in the industrial city environment was carried out during one year exposure. Corrosion potential was determined using the potentiometric method. The highest effect of corrosion processes was observed during the winter season due to increased air pollution. Corrosion of samples pre-treated in tannic acid before the exposure was more difficult compared with the s...

Atmospheric corrosion in subtropical areas: XRD and electrochemical study of zinc atmospheric corrosion products in the province of Santa Cruz de Tenerife (Canary Islands, Spain)

Energy Technology Data Exchange (ETDEWEB)

Morales, J. [Departamento de Quimica Fisica, Universidad de La Laguna, 38071 La Laguna, Tenerife (Spain)]. E-mail: jmorales@ull.es; Diaz, F. [Departamento de Quimica Fisica, Universidad de La Laguna, 38071 La Laguna, Tenerife (Spain); Hernandez-Borges, J. [Departamento de Quimica Analitica, Nutricion y Bromatologia, Universidad de La Laguna, 38071 La Laguna, Tenerife (Spain); Gonzalez, S. [Departamento de Quimica Fisica, Universidad de La Laguna, 38071 La Laguna, Tenerife (Spain)

2006-02-15

In the present paper, zinc sheets have been exposed for 4 years to the action of different atmospheres in 35 test sites located in the province of Santa Cruz de Tenerife, Canary Islands, Spain. Corrosion products formed on the surface of the samples have been identified by means of X-ray diffraction (XRD) for the first and second year of exposure. Zincite, hydrozincite, simonkolleite, zinc chlorohydroxysulphate, zinc oxysulphate and zinc hydroxysulphate have been identified in the test sheets. Preliminary results of an electrochemical study of the breakdown potential of zinc samples are also presented in order to test the protective effect of the film formed on the surface of the samples. It was found that the protective effect of this film increases linearly with exposure time.

Mechanisms of the multi-secular atmospheric corrosion of ferrous alloys: The case of the Metz cathedral reinforcements

International Nuclear Information System (INIS)

Bouchar, Marie

2015-01-01

The study of the mechanisms of the multi-secular atmospheric corrosion of ferrous alloys has various applications, from the preservation and restoration of cultural heritage metals, to the evaluation of their long term behaviour, specifically when they are used for the storage containers surrounding nuclear wastes. The study of the corrosion product layers (CPL) developed during 5 centuries on the Metz cathedral reinforcements brings new results for a better understanding of the complex processes involved in the formation of the atmospheric CPL. The phases and chemical elements constituting the CPL of these reinforcements were characterized at the micrometric scale (μDRX, Raman μ-spectroscopy (μRS), SEM-EDS). Results specifically showed that these CPL differ from other multi-secular systems previously studied by their very high content in ferri-hydrite (5Fe 2 O 3 , 9H 2 O). This very reactive phase is distributed in the whole CPL and mixed at the microscopic scale with goethite (a-FeOOH) and lepidocrocite (g-FeOOH). Diffusion experiments of bromide ions followed by in situ X-ray μ-fluorescence allowed a better understanding of the transport of dissolved species in the porous network of the CPL. Furthermore, a test of the corrosion system behavior in conditions simulating the wetting stage of the RH cycle of atmospheric corrosion, also followed in situ by μRS, highlighted the reduction of ferri-hydrite at the metal/CPL interface. These results allowed to verify for the first time a fundamental hypothesis about the mechanisms of very long term atmospheric corrosion. Finally, re-corrosion experiments of the corrosion system were monitored in a climatic chamber simulating accelerated atmospheric cycles in an 18 O-labelled environment. Then the detection of the 18 O isotope linked to the precipitated phases, by nuclear reaction analysis using a nuclear microprobe, allowed to localise the formation sites of the new corrosion products. All these results improve the

Corrosion in marine atmospheres. Effect of distance from the coast

International Nuclear Information System (INIS)

Chico, B.; Otero, E.; Morcillos, M.; Mariaca, L.

1998-01-01

In marine atmospheres the deposition of saline particles on the surface of metals intensifies the metallic corrosion process. However, quantitative information about the effect of atmospheric salinity on metallic corrosion is very scarce. This paper reports the relationship between salinity and metallic corrosion, where a clear linear relation (r=0.97) has been found for a broad interval of salinities (4-500 mg Cl''-/m''2.d), as well as the relationship between salinity (or metallic corrosion) and distance from the coast. A hyperbolic function seems to be established both variables; there is an exponential drop in salinity (or corrosion) as shoreline distance increases tending towards and asymptotic value. The study has been based on information obtained from field research conducted at a marine atmosphere in Tarragona (Spain) and data compiled from the literature. (Author) 14 refs

Atmospheric corrosion tests along the Norwegian-Russian border. Part II

Energy Technology Data Exchange (ETDEWEB)

Henriksen, J.F.; Mikhailov, A.A.

1997-12-31

A bilateral exposure programme was carried out along the Norwegian-Russian border in 1990-1991, 1992-1993 and 1993-1994 to evaluate quantitatively the effect of sulphur pollutants on the atmospheric corrosion of important materials in sub-arctic climate. The first part of the programme demonstrated that also in subarctic climate do metals corrode depending on the atmospheric corrosivity, and dose-response functions were derived which combined the effects of SO{sub 2} and time of wetness. The second part of the programme, which is described in this report, involved exposures of carbon steel, zinc and copper at two sites in Norway and three sites in Russia. It is concluded that the accelerated atmospheric corrosion of metals in regions along the border is mainly due to dry deposition of sulphur. At some sites, dry deposition of Cl contributes because of sea-salt aerosols. The corrosivity of acid precipitation is certain but could not be represented as a function because of the small differences observed in the pH values at the different sites. At all test sites the kinetics of corrosion of steel, zinc and copper are characterized by a reduced corrosion rate after one year of exposure. Time of wetness is an important parameter in predicting atmospheric corrosion of metals even on a regional scale. Hence, for monitoring and for trend-effect analysis, it is very important to determine the corrosivity of SO{sub 2} with time of wetness. In accordance with dose-response functions obtained, the yearly corrosion rate for steel and zinc are higher for the areas with higher amounts of dry deposition of Cl than for areas with analogous but only SO{sub 2}-containing atmosphere. 6 refs., 8 figs., 15 tabs.

Characterization of corrosion products of Zn and Zn–Mg–Al coated steel in a marine atmosphere

International Nuclear Information System (INIS)

Diler, E.; Rouvellou, B.; Rioual, S.; Lescop, B.; Nguyen Vien, G.; Thierry, D.

2014-01-01

Highlights: • The corrosion behaviour of Zn–Mg–Al alloy in marine environment is characterized. • Zn–Mg–Al alloy shows a better corrosion resistance than Zn. • Strong enhancement of NaZn 4 Cl(OH) 6 SO 4 ·6H 2 O in the corrosion products is observed. • Al 3+ and Mg 2+ induced quenching effects in corrosion activity are described. - Abstract: The corrosion behaviour of pure zinc and zinc–magnesium–aluminium alloy (ZMA) has been studied during 6 months of exposure in marine environment (Brest, France). The composition of corrosion products is analysed using infrared spectroscopy (FTIR), X-ray diffraction (XRD), and X-ray photoelectron spectroscopy (XPS). An improved corrosion resistance of ZMA is observed. This improvement is found to be connected to Mg 2+ and Al 3+ induced quenching of corrosion activity and to the enhancement of NaZn 4 Cl(OH) 6 SO 4 ·6H 2 O in the formed corrosion product

Timescale Correlation between Marine Atmospheric Exposure and Accelerated Corrosion Testing - Part 2

Science.gov (United States)

Montgomery, Eliza L.; Calle, Luz Marina; Curran, Jerome C.; Kolody, Mark R.

2012-01-01

Evaluation of metals to predict service life of metal-based structures in corrosive environments has long relied on atmospheric exposure test sites. Traditional accelerated corrosion testing relies on mimicking the exposure conditions, often incorporating salt spray and ultraviolet (UV) radiation, and exposing the metal to continuous or cyclic conditions similar to those of the corrosive environment. Their reliability to correlate to atmospheric exposure test results is often a concern when determining the timescale to which the accelerated tests can be related. Accelerated corrosion testing has yet to be universally accepted as a useful tool in predicting the long-term service life of a metal, despite its ability to rapidly induce corrosion. Although visual and mass loss methods of evaluating corrosion are the standard, and their use is crucial, a method that correlates timescales from accelerated testing to atmospheric exposure would be very valuable. This paper presents work that began with the characterization of the atmospheric environment at the Kennedy Space Center (KSC) Beachside Corrosion Test Site. The chemical changes that occur on low carbon steel, during atmospheric and accelerated corrosion conditions, were investigated using surface chemistry analytical methods. The corrosion rates and behaviors of panels subjected to long-term and accelerated corrosion conditions, involving neutral salt fog and alternating seawater spray, were compared to identify possible timescale correlations between accelerated and long-term corrosion performance. The results, as well as preliminary findings on the correlation investigation, are presented.

Real time corrosion monitoring in atmosphere using automated battery driven corrosion loggers

DEFF Research Database (Denmark)

Prosek, T.; Kouril, M.; Hilbert, Lisbeth Rischel

2008-01-01

diminishes due to corrosion. Zinc, iron, copper and nickel sensors at several thicknesses are available. Sensitivity of the corrosion measurement varies from 1 to 10 nm depending on the type and thickness of the sensor. Changes in the air corrosivity can be thus detected within hours or even tens of minutes......A logger enabling continuous measurement of corrosion rate of selected metals in indoor and outdoor atmospheres has been developed. Principle of the measurement method is based on the increasing electrical resistance of a measuring element made of the material concerned as its cross-sectional area....... The logger lifetime in medium corrosive environments is designed to be 2 years with full autonomy. Data on the sensor corrosion rate are available any time through GPRS connection or by a non-contact inductive reading without the need of retracting the logger from the exposure site....

Review: Results of studying atmospheric corrosion in Vietnam 1995–2005

Directory of Open Access Journals (Sweden)

Le Thi Hong Lien, Pham Thy San and Hoang Lam Hong

2007-01-01

Full Text Available Vietnam is situated in the wet tropical zone; thus, atmospheric conditions are characterized by high temperatures and a long time of wetness (TOW. In addition, the salt air coming in from the sea causes a high chloride concentration in coastal areas. Furthermore, Vietnam is a developing country, which means that air pollution is increasing with the development of industry. These factors result in significant damage to materials by atmospheric corrosion. In this report, the results of a recent study on the corrosion of carbon steel and zinc-galvanized steel at 6–8 testing sites in Vietnam over 10 recent years (1995–2005 are focused on as well as the effects of environmental factors on atmospheric corrosion. The results showed that the corrosion of carbon steel is dominated by TOW, whereas zinc-galvanized-steel corrosion strongly depends on the chloride ion concentration in the air. The corrosion losses of both carbon- and zinc-galvanized steel fit the power model well with high correlation coefficients. In addition, the characteristics of the Vietnamese climate are introduced in the form of distribution maps of temperature (T, relative humidity (RH, total rainfall and TOW. A relationship between TOW, T and RH was found that enabled the calculation of TOW from T and RH data, which are available at meteorological stations. Finally, atmospheric corrosivity is determined on the basis of data on TOW, Cl− and SO2 concentrations, and the carbon steel corrosion rate. It is shown that in Vietnam, TOW is so long that the corrosion rate of carbon steel is in the C3 category; nevertheless, Cl− and SO2 concentrations in the atmosphere are not high.

New fundamental and environmental aspects of atmospheric corrosion

Directory of Open Access Journals (Sweden)

Leygraf, C.

2009-06-01

Full Text Available Atmospheric corrosion involves chemical, electrochemical, and physical processes in three phases (solid, liquid, and gas and two interfaces (solid/liquid and liquid/gas. Because of inherent experimental and conceptual difficulties, scientific efforts to characterize this highly complex interfacial regime came relatively late into the field. With the access and development of surface and interface sensitive analytical techniques, it has lately become possible to perform molecular in situ analyses of the interfaces involved in atmospheric corrosion. This lecture presents some highlights from our fundamental research in atmospheric corrosion, performed at the Royal Institute of Technology in Stockholm, Sweden. It includes results from the most recent efforts in our research group to provide a molecular understanding of the interfacial regime that governs atmospheric corrosion. Using copper or zinc as substrate and carboxylic acid as corrosion stimulator in the humidity-containing atmosphere, results have been obtained with particular emphasis on probing the metal oxide/water interface (by infrared reflection absorption spectroscopy (IRAS combined with the quartz crystal microbalance (QCM and sum frequency generation (SFG and the water/gas interface (by SFG, respectively. While research in atmospheric corrosion traditionally has aimed at understanding how the environment influences the metal, the opposite question- how the metal influences the environment during atmospheric corrosion- may be of equally technical importance. Some examples of on-going research on new environmental aspects of atmospheric corrosion of zinc will also be presented.

La corrosión atmosférica implica procesos químicos, electroquímicos y físicos en tres fases (sólido, liquido y gas y dos interfases (sólido/líquido y líquido/gas. A causa de dificultades experimentales y conceptuales los esfuerzos científicos para caracterizar el proceso, interfacial

Long-Term Atmospheric Corrosion Behavior of Epoxy Prime Coated Aluminum Alloy 7075-T6 in Coastal Environment

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Sheng Zhang

2018-06-01

Full Text Available The atmospheric corrosion of epoxy prime coated aluminum alloy 7075-T6 exposed for 7, 12 and 20 years was investigated. The remaining thicknesses of epoxy prime coatings for macroscopically intact coating areas followed a normal distribution and decreased linearly. EIS results demonstrated that the corrosion resistance of the coating decreased with exposure time. After 20 years of exposure, the epoxy coating had lost its protection as cracks existed within the coating and exfoliation corrosion had occurred on the substrate. The substrate was sensitive to exfoliation corrosion through metallographic and TEM analysis. The corrosion products were mainly hydroxides of aluminum. The morphology and chemical compositions of the coating bubbling area and propagation characterizations of exfoliation corrosion were analyzed by SEM, EPMA and EDS. Cracks between the lumps of corrosion products provided the channels for the transmission of corrosion mediums. Furthermore, the mechanical model was proposed to analyze the propagation characterization of exfoliation corrosion.

Metallic corrosion in the polluted urban atmosphere of Hong Kong.

Science.gov (United States)

Liu, Bo; Wang, Da-Wei; Guo, Hai; Ling, Zhen-Hao; Cheung, Kalam

2015-01-01

This study aimed to explore the relationship between air pollutants, particularly acidic particles, and metallic material corrosion. An atmospheric corrosion test was carried out in spring-summer 2012 at a polluted urban site, i.e., Tung Chung in western Hong Kong. Nine types of metallic materials, namely iron, Q235 steel, 20# steel, 16Mn steel, copper, bronze, brass, aluminum, and aluminum alloy, were selected as specimens for corrosion tests. Ten sets of the nine materials were all exposed to ambient air, and then each set was collected individually after exposure to ambient air for consecutive 6, 13, 20, 27, 35, 42, 49, 56, 63, and 70 days, respectively. After the removal of the corrosion products on the surface of the exposed specimens, the corrosion rate of each material was determined. The surface structure of materials was observed using scanning electron microscopy (SEM) before and after the corrosion tests. Environmental factors including temperature, relative humidity, concentrations of gaseous pollutants, i.e., sulfur dioxide (SO₂), nitrogen dioxide (NO₂), carbon monoxide (CO), ozone (O₃), and particulate-phase pollutants, i.e., PM₂.₅ (FSP) and PM₁₀ (RSP), were monitored. Correlation analysis between environmental factors and corrosion rate of materials indicated that iron and carbon steel were damaged by both gaseous pollutants (SO₂ and NO₂) and particles. Copper and copper alloys were mainly corroded by gaseous pollutants (SO₂ and O₃), while corrosion of aluminum and aluminum alloy was mainly attributed to NO₂ and particles.

Corrosion study of steels exposed over five years to the humid tropical atmosphere of Panama

Energy Technology Data Exchange (ETDEWEB)

Jaén, Juan A., E-mail: juan.jaen@up.ac.pa [Departamento de Química Física, Edificio de Laboratorios Científicos-VIP (Panama); Iglesias, Josefina [Laboratorio de Análisis Industriales y Ciencias Ambientales (Panama)

2017-11-15

The results of assessing five-year corrosion of low-carbon and conventional weathering steels exposed to the Panamanian tropical atmosphere is presented. Two different test sites, one in Panama City: 5 km from the shoreline of the Pacific Ocean, and another in the marine environment of Fort Sherman, Caribbean coast of Panama; namely, Fort Sherman Coastal site: 100 m from coastline. The corrosion products, formed in the skyward and earthward faces in the studied tropical environment, were mainly identified using room temperature and low temperature (15 K) Mössbauer spectroscopy, and ATR-FTIR. In all samples, lepidocrocite (γ-FeOOH) and goethite (α-FeOOH) were the main constituents. Some maghemite (γ-Fe{sub 2}O{sub 3}), was also identified in Tocumen by Mössbauer spectroscopy and traces of feroxyhyte (δ-FeOOH) using ATR-FTIR. The corrosion rate values obtained are discussed in light of the atmospheric exposure conditions and atmospheric pollutants.

Atmospheric corrosion performance of different steels in early exposure in the coastal area region West Java, Indonesia

Science.gov (United States)

Nuraini, Lutviasari; Prifiharni, Siska; Priyotomo, Gadang; Sundjono, Gunawan, Hadi; Purawiardi, Ibrahim

2018-05-01

The performance of carbon steel, galvanized steel and aluminium after one month exposed in the atmospheric coastal area, which is in Limbangan and Karangsong Beach, West Java, Indonesia was evaluated. The corrosion rate was determined by weight loss method and the morphology of the steel after exposed was observed by Scanning Electron Microscopy(SEM)/Energy Dispersive X-Ray Analysis(EDX). The site was monitored to determine the chloride content in the marine atmosphere. Then, the corrosion products formed at carbon steel were characterized by X-Ray diffraction (XRD). The result showed the aggressively corrosion in Karangsong beach, indicated from the corrosion rate of carbon steel, galvanized steel and aluminium were 38.514 mpy; 4.7860 mpy and 0.5181 mpy, respectively. While in Limbangan Beach the corrosion rate of specimen carbon steel, galvanized steel and aluminium were 3.339; 0.219 and 0.166 mpy, respectively. The chloride content was found to be the main factor that influences in the atmospheric corrosion process in this area. Chloride content accumulated in Karangsong and Limbangan was 497 mg/m2.day and 117 mg/m2.day, respectively. The XRD Analysis on each carbon steel led to the characterization of a complex mixture of iron oxides phases.

Morphology of the ash corrosion products on the P92 steel

International Nuclear Information System (INIS)

Hernas, A.; Imosa, M.

2004-01-01

The P92 steel, owing to its high mechanical strength at an elevated temperature, is one of the new steel types intended for the components of modern boilers in the power engineering industry. Currently, attempts are being undertaken to use the P92 steel for the components of boiler units in municipal waste incineration plants. Therefore, it is important that an analysis be made of the P92 steel resistance to the high-temperature chlorine - sulfur corrosion impact, the latter being the main factor which limits durability of boilers in waste incineration plants. The present article presents the investigation of P92 steel corrosion resistance under the conditions of high-temperature chlorine- sulfur corrosion in an atmosphere of flue gas with ashes. The analyses were conducted by means of laboratory tests in an atmosphere containing sulfur and chlorine compounds. The morphology of corrosion products was determined by scanning microscopy and X-ray analysis methods. (author)

Annual and long-term prediction of the atmospheric corrosion of metals

International Nuclear Information System (INIS)

Morcillo, M.

1998-01-01

The atmospheric corrosion of metals is known to be a discontinuous electrochemical process which takes place only when the metallic surface is wet or moistened by different meteorological phenomena (rain, humidity condensation, fog, etc.) The magnitude of atmospheric corrosion would be relatively low if it were not for the presence of certain pollutants in the atmosphere, mainly sulphur dioxide (anthropogenic pollutant) and marine chlorides (natural pollutant). The literature contains different models for predicting the atmospheric metals over short periods (generally one year) and long periods (15, 20 or more years) of atmospheric exposure. In addition to the different meteorological factors (volume of precipitation, days of rain, relative humidity (RH), T, etc.), atmospheric SO 2 deposition rate and atmospheric salinity (Cl - ) appear as independent variables in all of these models. (Author)

The Moessbauer spectroscopy in the characterization of atmospheric corrosion products; La espectroscopia Moessbauer en la caracterizacion de productos de corrosion atmosferica

Energy Technology Data Exchange (ETDEWEB)

Hernandez Torres, D; Leiva Ronda, P [Centro de Estudios Aplicados al Desarrollo Nuclear (CEADEN), La Habana (Cuba); Gomez, J; Ronda, M [Centro de Investigaciones del Petroleo, La Habana (Cuba)

1996-07-01

A study of corrosion products on mild steel formed after 1 and 5 years exposure in two industrial coastal weathering stations in the Bay from Matanzas City, Cuba, has been carried out. Structural analysis was conducted using mainly transmission Moessbauer Spectroscopy and the X-ray diffraction as complementary technique. The main phases found in the specimen exposed to high chloride containing environment were: lepidocrocite ({gamma}- FeOOH), goethite ({alpha}- FeOOH) and magnetite concentration was the lowest, the phases found were {gamma}- FeOOH and {alpha}- FeOOH, and the phase transformation proposed was {gamma}- FeOOh -> {alpha}- Fe-OOH. In this station were found also amorphous corrosion products. There amorphous phases could be responsible for the lowest levels of corrosion on steel in this station.

Corrosion of bismuth-based superconductor wires by some atmospheric agents

International Nuclear Information System (INIS)

Ben Azzouz, F.; M'chirgui, A.; Ben Salem, M.; Yangui, B.; Lamine, C.; Nitsche, S.; Boulesteix, C.

2000-01-01

Superconducting wires (SWs) were previously prepared in our group by heat treatment of bismuth-based superconductor coatings on a metal core. This paper presents an analysis of the corrosion process by some atmospheric agents on the SWs. SWs with different concentrations of a (Bi, Pb)-2223 phase have been exposed to water vapour saturated air, to pure water vapour or to dry carbon dioxide. Each of these atmospheric agents was found to act differently on the SWs. However, all the studied corrosion processes present a high sensitivity to the concentration of the (Bi, Pb)-2223 phase. For a higher concentration of this phase, the SWs are less sensitive to atmospheric agents. (author)

Zn-10.2% Fe coating over carbon steel atmospheric corrosion resistance. Comparison with zinc coating

International Nuclear Information System (INIS)

Arnau, G.; Gimenez, E.; Rubio, M.V.; Saura, J.J.; Suay, J.J.

1998-01-01

Zn-10.2% Fe galvanized coating versus hot galvanized coating over carbon steel corrosion performance has been studied. Different periods of atmospheric exposures in various Valencia Community sites, and salt spray accelerated test have been done. Carbon steel test samples have been used simultaneously in order to classify exposure atmosphere corrosivity, and environmental exposure atmosphere characteristics have been analyzed. Corrosion Velocity versus environmental parameters has been obtained. (Author) 17 refs

Atmospheric corrosion: statistical validation of models

International Nuclear Information System (INIS)

Diaz, V.; Martinez-Luaces, V.; Guineo-Cobs, G.

2003-01-01

In this paper we discuss two different methods for validation of regression models, applied to corrosion data. One of them is based on the correlation coefficient and the other one is the statistical test of lack of fit. Both methods are used here to analyse fitting of bi logarithmic model in order to predict corrosion for very low carbon steel substrates in rural and urban-industrial atmospheres in Uruguay. Results for parameters A and n of the bi logarithmic model are reported here. For this purpose, all repeated values were used instead of using average values as usual. Modelling is carried out using experimental data corresponding to steel substrates under the same initial meteorological conditions ( in fact, they are put in the rack at the same time). Results of correlation coefficient are compared with the lack of it tested at two different signification levels (α=0.01 and α=0.05). Unexpected differences between them are explained and finally, it is possible to conclude, at least in the studied atmospheres, that the bi logarithmic model does not fit properly the experimental data. (Author) 18 refs

Kinetics of atmospheric corrosion of mild steel, zinc, galvanized iron and aluminium at 10 exposure stations in India

International Nuclear Information System (INIS)

Natesan, M.; Venkatachari, G.; Palaniswamy, N.

2006-01-01

As a part of updating Corrosion Map of India project, atmospheric corrosion behaviour of commercially available engineering materials such as mild steel, galvanized iron, zinc and aluminium metals was studied in marine, industrial, urban, and rural environments by weight loss method at 10 exposure stations in India over a period of 5 years. The results of these studies demonstrated that galvanized iron, zinc and aluminium metals were several times more durable than mild steel. Compared to galvanized iron and zinc, aluminium provided superior protection in industrial and marine environment except at Mormugao Port Trust (MPT). It also offered much better resistance to corrosion in rural environments. At certain places, galvanized iron proved to be more durable than aluminium. The results obeyed well with the empirical kinetics equation of the form C = Kt n , where K and C are the corrosion losses in μm after 1 and 't' years of the exposure, respectively, and 'n' is a constant. Based on 'n' values, the corrosion mechanisms of these metals are predicted. The corrosion products formed on the metal samples in Chennai marine atmosphere were identified by X-ray diffraction analysis

Moessbauer study of corrosion products formed on Fe80B20 and Fe40Ni40 (MoB)20 amorphous alloys in an SO2-polluted atmosphere

International Nuclear Information System (INIS)

Davalos, J.; Marco, J.F.; Gracia, M.; Gancedo, J.R.; Greneche, J.M.

1990-01-01

ICEMS, XPS, XRD, and AES have been used to study the corrosion layers formed on two metallic glasses, Fe 80 B 20 and Fe 40 Ni 40 (MoB) 20 (2605 and 2826 MB, Allied Company), exposed to an SO 2 -polluted humid atmosphere. The iron-containing corrosion products are the same found for pure iron in the same environment, but different relative concentrations were clearly evidenced by ICEMS results. Elemental sulphur, Ni(OH) 2 , and B(OH) 3 , the latter enriched at the surface, were found by XPS, XRD and AES. (orig.)

A brief review on the atmospheric corrosion of mild steel in Iran

Directory of Open Access Journals (Sweden)

E. Shafiei

2014-12-01

Full Text Available This paper presents a review on the atmospheric corrosion of steel, at three sites, in Iran. Corrosion rate values, time of wetness, and the level of pollutants, namely of SO2 and chlorides were determined for the first year of exposure in order to establish the aggressiveness of the atmospheres. The results obeyed well with the empirical kinetics equation of the form C = Ktn.

A Moessbauer and Electrochemical Characterization of the Corrosion Products Formed from Marine and Marine-Antartic Environments

Energy Technology Data Exchange (ETDEWEB)

Ohanian, M.; Caraballo, R.; Dalchiele, E. A.; Quagliata, E. [Instituto de Ingenieria Quimica, Facultad de Ingenieria (Uruguay)

2003-06-15

Corrosion products formed on low alloy steel under two marine environments are characterised. Both environments are classified as C4 according to the ISO 9223 Standard. The corrosion products are identified and their relative proportion is determined by Moessbauer spectroscopy (transmission geometry). Free potentials of corrosion are measured to evaluate the activity of their surfaces. Structural characterisation by XRD were performed on selected samples. It is concluded that the principal phases are goethite, lepidocrocite, ferrihidrite and maghemite. The relative amount of each of them changes with time and with the atmospheric dynamics of each environment.

A Moessbauer and Electrochemical Characterization of the Corrosion Products Formed from Marine and Marine-Antartic Environments

International Nuclear Information System (INIS)

Ohanian, M.; Caraballo, R.; Dalchiele, E. A.; Quagliata, E.

2003-01-01

Corrosion products formed on low alloy steel under two marine environments are characterised. Both environments are classified as C4 according to the ISO 9223 Standard. The corrosion products are identified and their relative proportion is determined by Moessbauer spectroscopy (transmission geometry). Free potentials of corrosion are measured to evaluate the activity of their surfaces. Structural characterisation by XRD were performed on selected samples. It is concluded that the principal phases are goethite, lepidocrocite, ferrihidrite and maghemite. The relative amount of each of them changes with time and with the atmospheric dynamics of each environment.

High-Temperature, Dual-Atmosphere Corrosion of Solid-Oxide Fuel Cell Interconnects

Science.gov (United States)

Gannon, Paul; Amendola, Roberta

2012-12-01

High-temperature corrosion of ferritic stainless steel (FSS) surfaces can be accelerated and anomalous when it is simultaneously subjected to different gaseous environments, e.g., when separating fuel (hydrogen) and oxidant (air) streams, in comparison with single-atmosphere exposures, e.g., air only. This so-called "dual-atmosphere" exposure is realized in many energy-conversion systems including turbines, boilers, gasifiers, heat exchangers, and particularly in intermediate temperature (600-800°C) planar solid-oxide fuel cell (SOFC) stacks. It is generally accepted that hydrogen transport through the FSS (plate or tube) and its subsequent integration into the growing air-side surface oxide layer can promote accelerated and anomalous corrosion—relative to single-atmosphere exposure—via defect chemistry changes, such as increased cation vacancy concentrations, decreased oxygen activity, and steam formation within the growing surface oxide layers. Establishment of a continuous and dense surface oxide layer on the fuel side of the FSS can inhibit hydrogen transport and the associated effects on the air side. Minor differences in FSS composition, microstructure, and surface conditions can all have dramatic influences on dual-atmosphere corrosion behaviors. This article reviews high-temperature, dual-atmosphere corrosion phenomena and discusses implications for SOFC stacks, related applications, and future research.

A discussion for stabilization time of carbon steel in atmospheric corrosion

Science.gov (United States)

Zhang, Zong-kai; Ma, Xiao-bing; Cai, Yi-kun

2017-09-01

Stabilization time is an important parameter in long-term prediction of carbon steel corrosion in atmosphere. The range of the stabilization time of carbon steel in atmospheric corrosion has been published in many scientific literatures. However, the results may not precise because engineering experiences is dominant. This paper deals with the recalculation of stabilization time based on ISO CORRAG program, and analyzes the results and makes a comparison to the data mentioned above. In addition, a new thinking to obtain stabilization time will be proposed.

corrosion problems and their relationship with the environment in the Colombian productive system

International Nuclear Information System (INIS)

Arroyave P, Carlos E; Herrera B, Francisco J; Delgado L, Juan; Cuervo T, Joaquin

1999-01-01

As a part of a broad study on the corrosion problems in the Colombian industry, it was included an assessment of the effect of the main corrosive environments (atmosphere, soil, salad and drinking water, and chemicals), on materials stability. On the other hand, the impact of the corrosion processes on the environmental constituents (live species, atmosphere, soil, materials, and water) was also assessed. Main conclusions are: Atmosphere is the more extensively corrosive environment, and, all the environmental constituents are affected by corrosion without significant differences

Indoor atmospheric corrosion of historical ferrous alloys. System characterisation, mechanisms and modelling discussion

International Nuclear Information System (INIS)

Monnier, J.

2008-12-01

Understanding the mechanisms of indoor atmospheric corrosion in iron alloys is of primary importance in several fields, including for the conservation of Middle Ages monuments or the long term storage of nuclear waste. In this research, a double approach was developed, combining fine characterisation of corrosion systems and design of experiments to answers specific questions related to mechanisms understanding. Iron indoor atmospheric corrosion was investigated on samples coming from the reinforcing chain of the Amiens cathedral (15. century). In the first stage, the corrosion system has been extensively characterised from the macroscopic to the nano-metric scale. In particular, structural micro-analysis (μ-Raman, μ-XRD, μ-XAS) has been used to locate, identify and quantify the oxidised phases. Rust layers are composed of a matrix of nano-metric goethite, with low quantities of lepidocrocite and akaganeite mostly located in the extern part of the corrosion system. In addition, clear marblings are dispersed in the matrix, which are sometimes connected with the metal core. Although these may contain maghemite, these marblings are generally made of ferri-hydrite/feroxyhite phases. In the second stage, specific experiments have been carried out in an unsaturated marked medium to locate oxygen reduction sites in the rust layers. Several cases were evidenced, depending on the rust layer morphology. In addition, reduction processes of model phases have been studied in situ, using an electrochemical cell coupled with structural characterisation techniques. This combination highlighted the influence of reduction mode and pH on the type of reduced phase formed. From the obtained results, several mechanisms are proposed to explain the long term indoor atmospheric corrosion of iron, including rust layers morphology and phases properties. The different hypotheses have been integrated in a proposed method to diagnosis ancient ferrous systems stability. These hypotheses also

The effect of surface treatment and gaseous rust protection paper on the atmospheric corrosion stability of aluminium alloy

International Nuclear Information System (INIS)

Gao Guizhong

1992-03-01

The experimental results of atmospheric corrosion of 166 aluminium alloy of Al-Mg-Si-Cu system and 167 aluminium alloy of Al-Mg-Si-Cu-Fe-Ni system for different surface treatment and different wrapping papers used are introduced. The results show: 1. The composition of aluminium alloy has some effect on the performance of atmospheric corrosion stability and the local corrosion depth for 167 aluminium alloy specimen is considerable. 2. After 8 years storage, the 167 aluminium alloy tubular specimen, which was treated with surface treatment in deionized water at 100 ∼ 230 C degree, has no spot of atmospheric corrosion found. 3. Within the test period, the performance of atmospheric corrosion stability by sulphuric-acid anodization film is remarkable. 4. The No. 19 gaseous rust protection paper has no effect of atmospheric corrosion stability on the 166 and 167 aluminium alloys which were treated with quenching and natural ageing method

Localized Corrosion Behavior of Type 304SS with a Silica Layer Under Atmospheric Corrosion Environments

International Nuclear Information System (INIS)

E. Tada; G.S. Frankel

2006-01-01

The U.S. Department of Energy (DOE) has proposed a potential repository for spent nuclear fuel and high-level radioactive waste at the Yucca Mountain site in Nevada. [I] The temperature could be high on the waste packages, and it is possible that dripping water or humidity could interact with rock dust particulate to form a thin electrolyte layer with concentrated ionic species. Under these conditions, it is possible that highly corrosion-resistant alloys (CRAs) used as packages to dispose the nuclear waste could suffer localized corrosion. Therefore, to better understand long-term corrosion performance of CRAs in the repository, it is important to investigate localized corrosion under a simulated repository environment. We measured open circuit potential (OCP) and galvanic current (i g ) for silica-coated Type 304SS during drying of salt solutions under controlled RH environments to clarify the effect of silica layer as a dust layer simulant on localized corrosion under atmospheric environments. Type 304SS was used as a relatively susceptible model CRA instead of the much more corrosion resistant alloys, such as Alloy 22, that are being considered as, waste package materials

Corrosion behaviors of SMART materials in the ammonia atmosphere

International Nuclear Information System (INIS)

Baek, J. H.; Lee, M. H.; Choi, B. S.; Kim, J. P.; Jung, Y. H.; Lee, D. J.

1999-01-01

The corrosion characteristics of the zirconium-based alloy(Low-Sn Zircaloy-4) and titanium-based alloys(PT-7M and ASTM Gr.2), which would be used for fuel cladding tube and steam generator tube in the SMART, were investigated at 360 deg C, 400 deg C, 500 deg C, and 520 deg C in the ammonia atmosphere. In all test conditions, the resistance to uniform and nodular corrosion of zirconium-based alloy was inferior to that of titanium-based alloys. In the case of 360 deg C test, the corrosion rate of zirconium-based alloy decreased slightly with increasing the ammonia concentration, while that of titanium-based alloys increased. The test results above 400 deg C showed that the corrosion resistance of PT-7M alloys was superior to that of ASTM Gr.2 alloy and was not influenced from the variation of ammonia concentration

Application Of Fractal Dimension On Atmospheric Corrosion Of Galvanized Iron Roofing Material

Directory of Open Access Journals (Sweden)

Issa A.K

2015-08-01

Full Text Available Abstract Corrosion rates of galvanized iron roofing sheet In yola north eastern part of Nigeria were assessed and determined by weight loss method and scanner fractal analysis method. Scanning electronic machine SEM was used to transform corrosion coupons to electronic form for image j processing and analysing software The result of corrosion rates for these two methods after six months of the samples exposure in industrial. Coastal market and urban areas in the region are 1.51 1.079 1.051 0.779 and 1.9941 1.9585 1.9565 1.9059 for weight loss and scanner fractal dimension methods respectively. and the results from the two methods were in agreement This establish the reliability of fractal dimension in measuring atmospheric corrosion this research also provides alternative method of measuring atmospheric corrosion and overcome the limitation of conventional weight loss technique in its inability to measure corrosion rate which is not significantly change over a long period of time moreover weight loss cannot demonstrate the area of concentration of corrosion on the surface of the coupon it rather gives the weight loss value and this will aid in determining the real level or extent of corrosion damage in the material and this can be obtained when measuring the material through fractal analysis these results clearly indicate that corrosion is heavier on locations close to the industrial areas. This also shows the negative impact of industrial activities on the corrodible materials and consequently on the plants and environment.

Atmospheric corrosion monitoring at the US Department of Energy's Oak Ridge K-25 Site

International Nuclear Information System (INIS)

Rao, M.

1995-01-01

Depleted uranium hexafluoride (UF 6 ) at the US Department of Energy's K-25 Site at Oak Ridge, TN has been stored in large steel cylinders which have undergone significant atmospheric corrosion damage over the last 35 years. A detailed experimental program to characterize and monitor the corrosion damage was initiated in 1992. Large amounts of corrosion scale and deep pits are found to cover cylinder surfaces. Ultrasonic wall thickness measurements have shown uniform corrosion losses up to 20 mils (0.5 mm) and pits up to 100 mils (2.5 mm) deep. Electrical resistance corrosion probes, time-of-wetness sensors and thermocouples have been attached to cylinder bodies. Atmospheric conditions are monitored using rain gauges, relative humidity sensors and thermocouples. Long-term (16 years) data are being obtained from mild steel corrosion coupons on test racks as well as attached directly to cylinder surfaces. Corrosion rates have been found to intimately related to the times-of-wetness, both tending to be higher on cylinder tops due to apparent sheltering effects. Data from the various tests are compared, discrepancies are discussed and a pattern of cylinder corrosion as a function of cylinder position and location is described

Mössbauer investigation of the influence of the sea atmosphere on the corrosion of steel constructions in Sochi

International Nuclear Information System (INIS)

Filippov, V. P.; Lauer, D. E.; Lauer, Yu. A.; Kargin, N. I.; Goloborodko, P. G.; Goloborodko, I. V.; Poliakov, A. M.

2013-01-01

A study of the sea atmosphere influence on the corrosion products of steel constructions near Sochi at difference distances from the sea has been made. The phases and compositions of the corrosion products formed on different sides of steel construction elements were examined by using Mössbauer spectroscopy (at 298 and 78 K). The results show that phases and composition distributions in oxide films are different on different parts of the constructions. The differences depend not only on the distance from the sea, but from their relative orientation to the sea also. The phase structure of the oxide films on different positions is identified.

VVER vessel steel corrosion at interaction with molten corium in oxidizing atmosphere

Energy Technology Data Exchange (ETDEWEB)

Bechta, S.V. [Alexandrov Research Institute of Technologies (NITI), Sosnovy Bor (Russian Federation)], E-mail: bechta@sbor.spb.su; Granovsky, V.S.; Khabensky, V.B.; Krushinov, E.V.; Vitol, S.A.; Sulatsky, A.A. [Alexandrov Research Institute of Technologies (NITI), Sosnovy Bor (Russian Federation); Gusarov, V.V.; Almiashev, V.I. [Institute of Silicate Chemistry, Russian Academy of Sciences (ISCh RAS), St. Petersburg (Russian Federation); Lopukh, D.B. [SPb State Electrotechnical University (SPbGETU), St. Petersburg (Russian Federation); Bottomley, D. [EUROPAISCHE KOMMISSION, Joint Research Centre Institut fuer Transurane (ITU), Karlsruhe (Germany); Fischer, M. [AREVA NP GmbH, Erlangen (Germany); Piluso, P. [CEA/DEN/DSNI, Saclay (France); Miassoedov, A.; Tromm, W. [Forschungszentrum Karlsruhe, Karlsruhe (Germany); Altstadt, E. [Forschungszentrum Rossendorf (FZR), Dresden (Germany); Fichot, F. [IRSN/DPAM/SEMCA, St. Paul lez Durance (France); Kymalainen, O. [FORTUM Nuclear Services Ltd., Espoo (Finland)

2009-06-15

The long-term in-vessel corium retention (IVR) in the lower head bears a risk of the vessel wall deterioration caused by steel corrosion. The ISTC METCOR Project has studied physicochemical impact of prototypic coria having different compositions in air and steam and has generated valuable experimental data on vessel steel corrosion. It is found that the corrosion rate is sensitive to corium composition, but the composition of oxidizing above-melt atmosphere (air, steam) has practically no influence on it. A model of the corrosion process that integrates the experimental data, is proposed and used for development of correlations.

VVER vessel steel corrosion at interaction with molten corium in oxidizing atmosphere

International Nuclear Information System (INIS)

Bechta, S.V.; Granovsky, V.S.; Khabensky, V.B.; Krushinov, E.V.; Vitol, S.A.; Sulatsky, A.A.; Gusarov, V.V.; Almiashev, V.I.; Lopukh, D.B.; Bottomley, D.; Fischer, M.; Piluso, P.; Miassoedov, A.; Tromm, W.; Altstadt, E.; Fichot, F.; Kymalainen, O.

2009-01-01

The long-term in-vessel corium retention (IVR) in the lower head bears a risk of the vessel wall deterioration caused by steel corrosion. The ISTC METCOR Project has studied physicochemical impact of prototypic coria having different compositions in air and steam and has generated valuable experimental data on vessel steel corrosion. It is found that the corrosion rate is sensitive to corium composition, but the composition of oxidizing above-melt atmosphere (air, steam) has practically no influence on it. A model of the corrosion process that integrates the experimental data, is proposed and used for development of correlations.

Some Clarifications Regarding Literature on Atmospheric Corrosion of Weathering Steels

Directory of Open Access Journals (Sweden)

I. Díaz

2012-01-01

Full Text Available Extensive research work has thrown light on the requisites for a protective rust layer to form on weathering steels (WSs in the atmosphere, one of the most important is the existence of wet/dry cycling. However, the abundant literature on WS behaviour in different atmospheres can sometimes be confusing and lacks clear criteria regarding certain aspects that are addressed in the present paper. What corrosion models best fit the obtained data? How long does it take for the rust layer to stabilize? What is the morphology and structure of the protective rust layer? What is an acceptable corrosion rate for unpainted WS? What are the guideline environmental conditions, time of wetness (TOW, SO2, and Cl−, for unpainted WS? The paper makes a review of the bibliography on this issue.

Insight into the product film formed on Ni-advanced weathering steel in a tropical marine atmosphere

Science.gov (United States)

Wu, Wei; Cheng, Xuequn; Hou, Huaxing; Liu, Bo; Li, Xiaogang

2018-04-01

The product film formed on Ni-advanced weathering steel in a tropical marine environment was investigated in detail through outdoor exposure by using diverse surface analysis techniques combined with electrochemical impedance spectroscopy and scanning kelvin probe measurements. The results showed that the product film was mainly composed of nanophasic goethite in the inner layer and maghemite, akaganeite, and hematite in the outer layer. Moreover, the resistance to atmospheric corrosion gradually increased from the outermost product film to the innermost film. Ni was significantly enriched in the inner layer in the form of the spinel phase NiFe2O4, which transformed lepidocrocite to fine-grained goethite, withstood the invasion of chloridion, and improved the corrosion potential of the product film in a tropical marine atmosphere.

Penetration of corrosion products and corrosion-induced cracking in reinforced cementitious materials

DEFF Research Database (Denmark)

Michel, Alexander; Pease, Brad J.; Peterova, Adela

2014-01-01

This paper describes experimental investigations on corrosion-induced deterioration in reinforced cementitious materials and the subsequent development and implementation of a novel conceptual model. Rejnforced mortar specimens of varying water-to-cement ratios were subjected to current-induced c......This paper describes experimental investigations on corrosion-induced deterioration in reinforced cementitious materials and the subsequent development and implementation of a novel conceptual model. Rejnforced mortar specimens of varying water-to-cement ratios were subjected to current......-dependent concentrations of corrosion products averaged through the specimen thickness. Digital image correlation (DIC) was used to measure corrosion-induced deformations including deformations between steel and cementitious matrix as well as formation and propagation of corrosion-induced cracks. Based on experimental...... observations, a conceptual model was developed to describe the penetration of solid corrosion products into capillary pores of the cementitious matrix. Only capillary pores within a corrosion accommodating region (CAR), i.e. in close proximity of the steel reinforcement, were considered accessible...

Corrosion-product inventory: the Bruce-B secondary system

International Nuclear Information System (INIS)

Sawicki, J.A.; Price, J.; Brett, M.E.

1995-01-01

Corrosion inspection and corrosion-product characterization in water and steam systems are important for component and systems maintenance in nuclear power stations. Corrosion products are produced, released and redeposited at various sites in the secondary system. Depending on the alloys used in the condenser and feedwater heaters, particulate iron oxides and hydroxides can account for about 95-99% of the total corrosion-product transport. Where brass or cupro-nickel alloys are present, copper and zinc contribute significantly to the total transport and deposition. Particulates are transported by the feedwater to the steam generators, where they accumulate and can cause a variety of problems, such as loss of heat transfer capability through deposition on boiler tubes, blockage of flow through boiler-tube support plates and accelerated corrosion in crevices, either in deep sludge piles or at blocked tube supports. The influx of oxidized corrosion products may have a particularly adverse effect on the redox environment of steam generator tubing, thereby increasing the probability of localized corrosion and other degradation mechanisms. In this paper, there is a description of a survey of general corrosion deposits in Bruce-B, Units 5-8, which helps to identify the origin, evolution and inventory of corrosion products along the secondary system of Candu reactors

Exposure testing of fasteners in preservative treated wood: Gravimetric corrosion rates and corrosion product analyses

Energy Technology Data Exchange (ETDEWEB)

Zelinka, Samuel L., E-mail: szelinka@fs.fed.u [USDA Forest Products Laboratory, One Gifford Pinchot Drive, Madison, WI 53726 (United States); Sichel, Rebecca J. [College of Engineering, University of Wisconsin, Madison, WI 53706 (United States); Stone, Donald S. [Department of Materials Science and Engineering, College of Engineering, University of Wisconsin, Madison, WI 53706 (United States)

2010-12-15

Research highlights: {yields} The composition of the corrosion products was similar for the nail head and shank. {yields} Reduced copper was not detected on any of the fasteners. {yields} Measured corrosion rates were between 1 and 35 {mu}m year{sup -1}. - Abstract: Research was conducted to determine the corrosion rates of metals in preservative treated wood and also understand the mechanism of metal corrosion in treated wood. Steel and hot-dip galvanized steel fasteners were embedded in wood treated with one of six preservative treatments and exposed to 27 {sup o}C at 100% relative humidity for 1 year. The corrosion rate was determined gravimetrically and the corrosion products were analyzed with scanning electron microscopy, energy dispersive X-ray spectroscopy, and X-ray diffraction. Although the accepted mechanism of corrosion in treated wood involves the reduction of cupric ions from the wood preservative, no reduced copper was found on the corrosion surfaces. The galvanized corrosion products contained sulfates, whereas the steel corrosion products consisted of iron oxides and hydroxides. The possible implications and limitations of this research on fasteners used in building applications are discussed.

49 CFR 195.583 - What must I do to monitor atmospheric corrosion control?

Science.gov (United States)

2010-10-01

... SAFETY TRANSPORTATION OF HAZARDOUS LIQUIDS BY PIPELINE Corrosion Control § 195.583 What must I do to... 49 Transportation 3 2010-10-01 2010-10-01 false What must I do to monitor atmospheric corrosion control? 195.583 Section 195.583 Transportation Other Regulations Relating to Transportation (Continued...

49 CFR 195.581 - Which pipelines must I protect against atmospheric corrosion and what coating material may I use?

Science.gov (United States)

2010-10-01

... corrosion and what coating material may I use? 195.581 Section 195.581 Transportation Other Regulations... Corrosion Control § 195.581 Which pipelines must I protect against atmospheric corrosion and what coating... atmosphere, except pipelines under paragraph (c) of this section. (b) Coating material must be suitable for...

Experimental Study of Removing Surface Corrosion Products from Archaeological Iron Objects and Alternating Iron Corrosion Products by Nd:YAG Laser Cleaning System

Energy Technology Data Exchange (ETDEWEB)

Lee, Hye Youn; Cho, Nam Chul [Kongju National University, Daejeon (Korea, Republic of); Lee, Jong Myoung [IMT co. Ltd, Suwon (Korea, Republic of); Yu, Jae Eun [National Research Institute of Cultural Heritage, Daejeon (Korea, Republic of)

2012-05-15

The corrosion product of archaeological iron objects is supposed to be removed because it causes re-corrosion. So far it is removed by scapel and sand blaster but they depend on the skill and experience of a conservator and the glass-dust of the sand blaster is harmful to humans. Therefore this study applies a laser cleaning system which is used in various industrial cleaning processes, to remove corrosion product from archaeological iron objects. In addition, this work studies the alternation of corrosion product after laser irradiation, which evaluates the reliability of the laser cleaning system. Optical microscopy, SEM-EDS, XRD, Raman have been used to observe and analyse the surface of the objects. The results show the capacity of laser cleaning some corrosion product, but blackening appears with increasing pulses and laser energy, and some corrosion products, goethite and hematite, are partially altered to magnetite. These problems, blackening and alternation of corrosion product, should be solved by further studies which find the optimal laser irradiation condition and use a wetting agent.

Techniques for the identification of corrosion products

International Nuclear Information System (INIS)

Ramanathan, L.V.

1988-12-01

This paper presents the different techniques that can be used to identify corrosion/oxidation products through determination of either their composition or their structure, chemical analysis and spectrochemical analysis are commonly used to determine the composition of gross corrosion products. Surface anaLysis techniques such as electron microprobe, AES, ESCA, SIMS, ISS, neutron activation analysis, etc., can be used not only to detect the concentration of the various elements present, but also to obtain the concentration profiles of these elements through the corrosion products. The structure of corrosion products is normally determined with the aid of either X-ray or electron diffraction techniques. This paper describes the basic principles, typical characteristics, limitations and the types of information that can be obtained from each of the techniques along with some typical examples. (author) [pt

Corrosion products in power generating systems

International Nuclear Information System (INIS)

Lister, D.H.

1980-06-01

The important mechanisms of corrosion and corrosion product movement and fouling in the heat transport systems of thermal electric generating stations are reviewed. Oil- and coal-fired boilers are considered, along with nuclear power systems - both direct and indirect cycle. Thus, the fireside and waterside in conventional plants, and the primary coolant and steam-raising circuits in water-cooled reactors, are discussed. Corrosion products in organic- and liquid-metal-cooled reactors also are shown to cause problems if not controlled, while their beneficial effects on the cooling water side of condensers are described. (auth)

Spectrophotometric Method for the Determination of Atmospheric Cr Pollution as a Factor to Accelerated Corrosion

Directory of Open Access Journals (Sweden)

Dereje Homa

2017-01-01

Full Text Available The effect of Cr(VI pollution on the corrosion rate of corrugated iron roof samples collected from tanning industry areas was investigated through simulated laboratory exposure and spectrophotometric detection of Cr(III deposit as a product of the reaction. The total level of Cr detected in the samples ranged from 113.892 ± 0.17 ppm to 53.05 ± 0.243 ppm and showed increasing trend as sampling sites get closer to the tannery and in the direction of tannery effluent stream. The laboratory exposure of a newly manufactured material to a simulated condition showed a relatively faster corrosion rate in the presence of Cr(VI with concomitant deposition of Cr(III under pH control. A significant (P = 0.05 increase in the corrosion rate was also recorded when exposing scratched or stress cracked samples. A coupled redox process where Cr(VI is reduced to a stable, immobile, and insoluble Cr(III accompanying corrosion of the iron is proposed as a possible mechanism leading to the elevated deposition of the latter on the materials. In conclusion, the increased deposits of Cr detected in the corrugated iron roof samples collected from tanning industry zones suggested possible atmospheric Cr pollution as a factor to the accelerated corrosion of the materials.

Spectrophotometric Method for the Determination of Atmospheric Cr Pollution as a Factor to Accelerated Corrosion.

Science.gov (United States)

Homa, Dereje; Haile, Ermias; Washe, Alemayehu P

2017-01-01

The effect of Cr(VI) pollution on the corrosion rate of corrugated iron roof samples collected from tanning industry areas was investigated through simulated laboratory exposure and spectrophotometric detection of Cr(III) deposit as a product of the reaction. The total level of Cr detected in the samples ranged from 113.892 ± 0.17 ppm to 53.05 ± 0.243 ppm and showed increasing trend as sampling sites get closer to the tannery and in the direction of tannery effluent stream. The laboratory exposure of a newly manufactured material to a simulated condition showed a relatively faster corrosion rate in the presence of Cr(VI) with concomitant deposition of Cr(III) under pH control. A significant ( P = 0.05) increase in the corrosion rate was also recorded when exposing scratched or stress cracked samples. A coupled redox process where Cr(VI) is reduced to a stable, immobile, and insoluble Cr(III) accompanying corrosion of the iron is proposed as a possible mechanism leading to the elevated deposition of the latter on the materials. In conclusion, the increased deposits of Cr detected in the corrugated iron roof samples collected from tanning industry zones suggested possible atmospheric Cr pollution as a factor to the accelerated corrosion of the materials.

Corrosion-product transport, oxidation state and remedial measures

International Nuclear Information System (INIS)

Sawicki, J.A.; Brett, M.E.; Tapping, R.L.

1998-01-01

The issues associated with monitoring and controlling corrosion-product transport (CPT) in the balance-of-plant (BOP) and steam generators (SG) of CANDU stations are briefly reviewed. The efforts are focused on minimizing corrosion of carbon steel, which is used extensively in the CANDU primary and secondary systems. Emphasis is placed on the corrosion-product oxidation state as a monitor of water chemistry effectiveness, and as a monitor of system corrosion effects. The discussion is based mostly on the results and observations from Ontario Hydro plants, and their comparisons with PWRs. The effects of low oxygen and elevated hydrazine chemistry are reviewed, as well as the effects of lay-up and various start-up conditions. Progress in monitoring electrochemical potential (ECP) at Ontario Hydro plants and its relationship to the oxidation state of corrosion products is reviewed. Observations on corrosion-product transport on the primary side of steam generators are also discussed. (author)

Effect of Ni on the corrosion resistance of bridge steel in a simulated hot and humid coastal-industrial atmosphere

Science.gov (United States)

Li, Dong-liang; Fu, Gui-qin; Zhu, Miao-yong; Li, Qing; Yin, Cheng-xiang

2018-03-01

The corrosion resistance of weathering bridge steels containing conventional contents of Ni (0.20wt%, 0.42wt%, 1.50wt%) and a higher content of Ni (3.55wt%) in a simulated hot and humid coastal-industrial atmosphere was investigated by corrosion depth loss, scanning electron microscopy-energy-dispersive X-ray spectroscopy, Raman spectroscopy, X-ray diffraction, X-ray photoelectron spectroscopy, and electrochemical methods. The results showed that, with increasing Ni content, the mechanical properties of the bridge steel were markedly improved, the welding parameters were satisfactory at room temperature, and the corrosion resistance was enhanced. When the Ni content was low (≤0.42wt%), the crystallization process of the corrosion products was substantially promoted, enhancing the stability of the rust layer. When the Ni content was higher ( 3.55wt%), the corrosion reaction of the steel quickly reached a balance, because the initial rapid corrosion induced the formation of a protective rust layer in the early stage. Simultaneously, NiO and NiFe2O2 were generated in large quantities; they not only formed a stable, compact, and continuous oxide protective layer, but also strongly inhibited the transformation process of the corrosion products. This inhibition reduced the structural changes in the rust layer, thereby enhancing the protection. However, when the Ni content ranged from 0.42wt% to 1.50wt%, the corrosion resistance of the bridge steel increased only slightly.

Regularities of transition of steel corrosion products into aqueous medium

International Nuclear Information System (INIS)

Nikitin, V.I.; Gvozd', A.M.; Karpova, T.Ya.

1981-01-01

Effect of different factors on a degree of steel corrosion product transition to a water medium has been studied. Ratio of a specific masm qsub(c) of the corrosion products transferring to the water and a specific masm q of all the steel corrosion products produced under the given conditions was used as a criterium characterizing a degree of corrosion product transition from steel surfaces to water. The transition degree to water at a high temperature of different kind steel corrosion products differs relatively few (qsub(c)/q=0.5-0.7) in the water containing oxygen and different salts on increasing temperature, the corrosion process is characterized with continuous decrease of a relative amount of the corrosion products transferring to the medium. On the contrary, in the deaerated water the transition degree of perlite steel corrosion products to water remains constant in a wide temperature range (100-320 deg C). Besides chromium, nickel being a part of austenitic steel composition affects positively decrease of the transition degree of the corrosion products to water as well as q and qsub(c) reduction. The most difference in corrosion characteristics and the transition degree to water is observed when affecting colant steels in the low-temperature zone of the steam generator [ru

Corrosion behaviors and effects of corrosion products of plasma electrolytic oxidation coated AZ31 magnesium alloy under the salt spray corrosion test

International Nuclear Information System (INIS)

Wang, Yan; Huang, Zhiquan; Yan, Qin; Liu, Chen; Liu, Peng; Zhang, Yi; Guo, Changhong; Jiang, Guirong; Shen, Dejiu

2016-01-01

Highlights: • Corrosion behaviors of a PEO coating was investigated after the salt spray test. • Corrosion products have significant effects on corrosion behaviors of the coating. • An electrochemical corrosion model is proposed. - Abstract: The effects of corrosion products on corrosion behaviors of AZ31 magnesium alloy with a plasma electrolytic oxidation (PEO) coating were investigated under the salt spray corrosion test (SSCT). The surface morphology, cross-sectional microstructure, chemical and phase compositions of the PEO coating were determined using scanning electron microscopy (SEM) equipped with energy dispersive X-ray spectroscopy (EDS) and X-ray diffraction analysis (XRD), respectively. Further, the corrosion process of the samples under the SSCT was examined in a non-aqueous electrolyte (methanol) using electrochemical impedance spectroscopy (EIS) coupled with equivalent circuit. The results show that the inner layer of the coating was destroyed firstly and the corrosion products have significant effects on the corrosion behaviors of the coating. The results above are discussed and an electrochemical corrosion model is proposed in the paper.

Corrosion behaviors and effects of corrosion products of plasma electrolytic oxidation coated AZ31 magnesium alloy under the salt spray corrosion test

Energy Technology Data Exchange (ETDEWEB)

Wang, Yan; Huang, Zhiquan; Yan, Qin; Liu, Chen; Liu, Peng; Zhang, Yi [State Key Laboratory of Metastable Materials Science and Technology, College of Materials Science and Engineering, Yanshan University, Qinhuangdao 066004 (China); Guo, Changhong; Jiang, Guirong [College of Mechanical Engineering, Yanshan University, Qinhuangdao 066004 (China); Shen, Dejiu, E-mail: DejiuShen@163.com [State Key Laboratory of Metastable Materials Science and Technology, College of Materials Science and Engineering, Yanshan University, Qinhuangdao 066004 (China)

2016-08-15

Highlights: • Corrosion behaviors of a PEO coating was investigated after the salt spray test. • Corrosion products have significant effects on corrosion behaviors of the coating. • An electrochemical corrosion model is proposed. - Abstract: The effects of corrosion products on corrosion behaviors of AZ31 magnesium alloy with a plasma electrolytic oxidation (PEO) coating were investigated under the salt spray corrosion test (SSCT). The surface morphology, cross-sectional microstructure, chemical and phase compositions of the PEO coating were determined using scanning electron microscopy (SEM) equipped with energy dispersive X-ray spectroscopy (EDS) and X-ray diffraction analysis (XRD), respectively. Further, the corrosion process of the samples under the SSCT was examined in a non-aqueous electrolyte (methanol) using electrochemical impedance spectroscopy (EIS) coupled with equivalent circuit. The results show that the inner layer of the coating was destroyed firstly and the corrosion products have significant effects on the corrosion behaviors of the coating. The results above are discussed and an electrochemical corrosion model is proposed in the paper.

Corrosion/95 conference papers

International Nuclear Information System (INIS)

Anon.

1995-01-01

The papers in this conference represent the latest technological advances in corrosion control and prevention. The following subject areas are covered: cathodic protection in natural waters; materials for fossil fuel combustion and conversion systems; modern problems in atmospheric corrosion; innovative ideas for controlling the decaying infrastructure; deposits and their effects on corrosion in industry; volatile high temperature and non aqueous corrosion inhibitors; corrosion of light-weight and precoated metals for automotive application; refining industry corrosion; corrosion in pulp and paper industry; arctic/cold weather corrosion; materials selection for waste incinerators and associated equipment; corrosion measurement technology; environmental cracking of materials; advancing technology in the coating industry; corrosion in gas treating; green inhibition; recent advances in corrosion control of rail equipment; velocity effects and erosion corrosion in oil and gas production; marine corrosion; corrosion of materials in nuclear systems; underground corrosion control; corrosion in potable and industrial water systems in buildings and its impact on environmental compliance; deposit related boiler tube failures; boiler systems monitoring and control; recent developments and experiences in reactive metals; microbiologically influenced corrosion; corrosion and corrosion control for steel reinforced concrete; international symposium on the use of 12 and 13 Cr stainless steels in oil and gas production environments; subsea corrosion /erosion monitoring in production facilities; fiberglass reinforced pipe and tubulars in oilfield service; corrosion control technology in power transmission and distribution; mechanisms and methods of scale and deposit control; closing the loop -- results oriented cooling system monitoring and control; and minimization of aqueous discharge

Aluminum corrosion product release kinetics

Energy Technology Data Exchange (ETDEWEB)

Edwards, Matt, E-mail: Matthew.Edwards@cnl.ca; Semmler, Jaleh; Guzonas, Dave; Chen, Hui Qun; Toor, Arshad; Hoendermis, Seanna

2015-07-15

Highlights: • Release of Al corrosion product was measured in simulated post-LOCA sump solutions. • Increased boron was found to enhance Al release kinetics at similar pH. • Models of Al release as functions of time, temperature, and pH were developed. - Abstract: The kinetics of aluminum corrosion product release was examined in solutions representative of post-LOCA sump water for both pressurized water and pressurized heavy-water reactors. Coupons of AA 6061 T6 were exposed to solutions in the pH 7–11 range at 40, 60, 90 and 130 °C. Solution samples were analyzed by inductively coupled plasma atomic emission spectroscopy, and coupon samples were analyzed by secondary ion mass spectrometry. The results show a distinct “boron effect” on the release kinetics, expected to be caused by an increase in the solubility of the aluminum corrosion products. New models were developed to describe both sets of data as functions of temperature, time, and pH (where applicable)

Behaviour of steel corrosion products under neutral-oxidizing water conditions

International Nuclear Information System (INIS)

Martynova, O.I.; Petrova, T.I.; Samojlov, Yu.F.; Kharitonova, N.L.

1985-01-01

Results of laboratory experiments on studying the solubility of iron and cobalt corrosion products are given. It is established that oxygen dosage doesn't influence practically on the iron corrosion product solubility but cobalt corrosion product solubility decreases, the presence of hydrogen peroxide in an initial solution leads to increase of the iron corrosion product solubility especially at 125 deg C. It is shown that hydrogen peroxide affects unambiguously the cobalt corrosion product solubility: at hydrogen peroxide concentration of about 400 μg/l at 50-275 deg C temperature their solubility is minimum

Electrochemical properties of corrosion products formed on Zn-Mg, Zn-Al and Zn-Al-Mg coatings in model atmospheric conditions

Czech Academy of Sciences Publication Activity Database

Stoulil, J.; Prošek, T.; Nazarov, A.; Oswald, Jiří; Kříž, P.; Thierry, D.

2015-01-01

Roč. 66, č. 8 (2015), s. 777-782 ISSN 0947-5117 Institutional support: RVO:68378271 Keywords : corrosion products * electrochemical properties * zinc coating Subject RIV: JK - Corrosion ; Surface Treatment of Materials Impact factor: 1.450, year: 2015

Influence of temperature on corrosion rate and porosity of corrosion products of carbon steel in anoxic bentonite environment

International Nuclear Information System (INIS)

Stoulil, J.; Kaňok, J.; Kouřil, M.; Parschová, H.; Novák, P.

2013-01-01

Highlights: •The corrosion rate is not significantly dependent on temperature. •Corrosion products at higher temperatures have different color. •Corrosion products at higher temperatures are more compact. •The change in corrosion products nature is reversible. -- Abstract: The study focuses on the porosity of layers of corrosion products and its impact on corrosion rate of carbon steel in moist bentonite. Measurements were performed in an aggressive Czech type of bentonite – Rokle B75 at temperatures of 90 and 40 °C. Aggressiveness of B75 bentonite consists in low content of chlorides. Presence of chlorides in pore solution allows formation of more protective magnetite. The evaluation was made by electrochemical techniques (red/ox potential, open circuit potential, linear polarization resistance, impedance spectroscopy) and resistometric sensor measurements. The result imply that the higher the temperature the more compact is the layer of corrosion products that slightly decelerates corrosion rate compared to the state at 40 °C. The state of corrosion products at both temperatures is reversible

Influence of temperature on corrosion rate and porosity of corrosion products of carbon steel in anoxic bentonite environment

Energy Technology Data Exchange (ETDEWEB)

Stoulil, J., E-mail: jan.stoulil@vscht.cz [Department of Metals and Corrosion Engineering, Institute of Chemical Technology, Prague (Czech Republic); Kaňok, J.; Kouřil, M. [Department of Metals and Corrosion Engineering, Institute of Chemical Technology, Prague (Czech Republic); Parschová, H. [Department of Power Engineering, Institute of Chemical Technology, Prague (Czech Republic); Novák, P. [Department of Metals and Corrosion Engineering, Institute of Chemical Technology, Prague (Czech Republic)

2013-11-15

Highlights: •The corrosion rate is not significantly dependent on temperature. •Corrosion products at higher temperatures have different color. •Corrosion products at higher temperatures are more compact. •The change in corrosion products nature is reversible. -- Abstract: The study focuses on the porosity of layers of corrosion products and its impact on corrosion rate of carbon steel in moist bentonite. Measurements were performed in an aggressive Czech type of bentonite – Rokle B75 at temperatures of 90 and 40 °C. Aggressiveness of B75 bentonite consists in low content of chlorides. Presence of chlorides in pore solution allows formation of more protective magnetite. The evaluation was made by electrochemical techniques (red/ox potential, open circuit potential, linear polarization resistance, impedance spectroscopy) and resistometric sensor measurements. The result imply that the higher the temperature the more compact is the layer of corrosion products that slightly decelerates corrosion rate compared to the state at 40 °C. The state of corrosion products at both temperatures is reversible.

Investigation of the cut-edge corrosion of organically-coated galvanized steel after accelerated atmospheric corrosion test

Directory of Open Access Journals (Sweden)

Reşit Yıldız

2015-11-01

Full Text Available The cut edge corrosion of organically coated (epoxy, polyurethane and polyester galvanized steel was investigated using electrochemical impedance spectroscopy (EIS. Measurements were performed on specimens that had been tested in an accelerated atmospheric corrosion test. The samples were subjected to 10 s fogging and 1 h awaiting cycles in an exposure cabinet (120 and 180 days with artificial acid rain solution. According to the investigation, the coatings were damaged from the cut edge into the sheet, this distance was about 0.8 cm. These defects were more pronounced at after 180 days in proportion to after 120 days.

Durability of bare and anodised aluminium in atmosphere of very different corrosivities I. Bare aluminium

International Nuclear Information System (INIS)

Gonzalez, J. A.; Escudero, E.; Lopez, V.; Simancas, J.; Morcillo, M.

2004-01-01

The behaviour of bare aluminium is studied in atmospheric exposure at 11 natural testing stations with salinity levels ranging between 2.1 and 684 mg Cl''- m''-2 d''-1. In atmospheres of low or moderate aggressivity aluminium behaves as a passive material, though the insignificant corrosion that is produced is sufficient to spoil its appearance. In contrast, at salinity levels of 50 mg Cl''- m''-2 ''-1 or above, aluminium is susceptible to pitting corrosion even in the first year of atmospheric exposure, or in the second year at salinities of ≤ 10 mg Cl''- m''-2 d''-1. For comparative purposes, results are included for aluminium protected with an anodic film of 28 μm thickness exposed at the same testing stations. A 28 μm anodic film, correctly sealed, prevents the risk of localised corrosion even in the most unfavourable situations. (Author) 23 refs

Study on corrosion products from ear piercing studs

International Nuclear Information System (INIS)

Rogero, Sizue O.; Costa, Isolda; Saiki, Mitiko

2000-01-01

In this work instrumental neutron activation analysis was applied to analyse elemental composition of commercial gold coated ear piercing substrate and metals present in their corrosion products. The cytotoxic effect was also verified in these corrosion product extracts, probably, due to the lixiviation of Ni present in high quantity in their substrates. The analysis of gold coated ear piercing surfaces by scanning electron microscopy before and after the corrosion test showed coating defects and the occurrence of corrosion process. (author)

Mechanism of Early Stage Corrosion for Boric-sulfuric Acid Anodized 2A97 Al-Cu-Li Alloy Under Tropical Marine Atmosphere

Directory of Open Access Journals (Sweden)

LUO Chen

2016-09-01

Full Text Available Optical microscopy(OM, scanning electron microscopy(SEM, EDX and EIS combined with ultramicrotomy were employed to investigate the micro morphology, chemical composition and electrochemical properties of anodized 2A97 Al-Cu-Li alloy before and after atmospheric corrosion. The results show that when electrolytes containing combinations of tartaric-sulfuric or boric-sulfuric acid are used to grow the films at different temperatures, boric acid addition and higher temperature allow for higher current density that speeds up the film growth. The pore geometry and structure is similar for different electrolytes. Dispersive dark rusty spots composed of O, Al, Cl, Cu are present on the boric-sulfuric acid anodized specimen after exposure in tropical marine atmosphere for 1 month. Deposition of white corrosion product is found on the specimen surface as well. Severe pitting occurs and develops deeply into the alloy substrate after elongated outdoor exposure. Corrosion propagation is associated with θ-phase particles.

Device of capturing for radioactive corrosion products

International Nuclear Information System (INIS)

Ohara, Atsushi; Fukushima, Kimichika.

1984-01-01

Purpose: To increase the area of contact between the capturing materials for the radioactive corrosion products contained in the coolants and the coolants by producing stirred turbulent flows in the coolant flow channel of LMFBR type reactors. Constitution: Constituent materials for the nuclear fuel elements or the reactor core structures are activated under the neutron irradiation, corroded and transferred into the coolants. While capturing devices made of pure metal nickel are used for the elimination of the corrosion products, since the coolants form laminar flows due to the viscosity thereof near the surface of the capturing materials, the probability that the corrosion products in the coolants flowing through the middle portion of the channel contact the capturing materials is reduced. In this invention, rotating rolls and flow channels in which the balls are rotated are disposed at the upstream of the capturing device to forcively disturb the flow of the liquid sodium, whereby the radioactive corrosion products can effectively be captured. (Kamimura, M.)

57Fe Moessbauer spectroscopic study on surface products of thin iron plates exposed to ambient atmosphere as a means of environmental monitoring

International Nuclear Information System (INIS)

Matsuo, Motoyuki; Kobayashi, Takaaki

1993-01-01

Conversion electron and transmission Moessbauer spectroscopy were applied to the analysis of thin iron plates exposed to the ambient atmosphere. The degree of corrosion of the iron plates was classified into three categories according to the kind and thickness of rust evaluated by Moessbauer spectra. The severe corrosion took place in seaside and roadside areas. The medium corrosion was observed in urban areas, and the weak corrosion occurred in suburban and mountainous areas. This fact implies that the surface products of iron plates can successfully reflect the ambient atmosphere to which the plates were exposed. (orig.)

High Temperature Corrosion under Laboratory Conditions Simulating Biomass-Firing: A Comprehensive Characterization of Corrosion Products

DEFF Research Database (Denmark)

Okoro, Sunday Chukwudi; Montgomery, Melanie; Jappe Frandsen, Flemming

2014-01-01

characterization of the corrosion products. The corrosion products consisted of three layers: i) the outermost layer consisting of a mixed layer of K2SO4 and FexOy on a partly molten layer of the initial deposit, ii) the middle layer consists of spinel (FeCr2O4) and Fe2O3, and iii) the innermost layer is a sponge......-like Ni3S2 containing layer. At the corrosion front, Cl-rich protrusions were observed. Results indicate that selective corrosion of Fe and Cr by Cl, active oxidation and sulphidation attack of Ni are possible corrosion mechanisms....

Emissions of the corrosion radionuclides in an atmosphere

International Nuclear Information System (INIS)

Vardanyan, M.

2010-01-01

In area of Armenian nuclear power plant location, in atmospheric air in majority of cases log two technogenic radionuclides: l 37 C s and 9 0 S r. Presence of these radionuclides basically is caused by global fall out (consequences of tests of the nuclear weapon and Chernobyl NPP accident), whose contribution to the contents of these radionuclides in atmosphere is incomparably greater, than emissions from the NPP. However there are some cases when in an atmosphere are registered the technogenic radionuclides, caused by emissions from NPP. In the present work such case is considered. Gas-aerosol releases of NPP in the atmosphere are carefully purified by means of various high-efficiency filters and gas-cleaning systems. Nevertheless, one should forecast and measure, the possible impact of these releases on the environment in the regions surrounding the NPP. Radioactive releases of the Armenian NPP (ANPP) contain the set of radionuclides characteristic for NPPs of this type. They may be divided into three groups: 1 31 I , 1 37 C s, 1 34 C s, 9 0 S r and 8 9 S r fission fragments, isotopes of noble gases krypton and xenon and other radionuclides; corrosion originated radionuclides: 6 0 C o, 1 10m A g, 5 4 M n, 5 l C r and others; activation products of the heat-transfer agent itself. It should be noted that the amount of radioactive materials released in the environment by the ANPP during the whole period of its operation was much lower than the admissible quantities specified in the corresponding legal documents (RSN, NPPSP) acting in Armenia, which are practically identical to the internationally accepted norms. The amounts of releases and their radionuclides composition for the ANPP are given

Spatial distribution of crystalline corrosion products formed during corrosion of stainless steel in concrete

Energy Technology Data Exchange (ETDEWEB)

Serdar, Marijana [Department of Materials, Faculty of Civil Engineering, University of Zagreb, 10000 Zagreb (Croatia); Meral, Cagla [Middle East Technical University, Department of Civil Engineering, Ankara (Turkey); Kunz, Martin [Lawrence Berkeley National Laboratory, 1 Cyclotron Road, Berkeley, CA 94720 (United States); Bjegovic, Dubravka [Department of Materials, Faculty of Civil Engineering, University of Zagreb, 10000 Zagreb (Croatia); Wenk, Hans-Rudolf [Department of Earth and Planetary Science, University of California, Berkeley, CA 94720 (United States); Monteiro, Paulo J.M., E-mail: monteiro@ce.berkeley.edu [Department of Civil and Environmental Engineering, University of California, Berkeley, CA 94720 (United States)

2015-05-15

The mineralogy and spatial distribution of nano-crystalline corrosion products that form in the steel/concrete interface were characterized using synchrotron X-ray micro-diffraction (μ-XRD). Two types of low-nickel high-chromium reinforcing steels embedded into mortar and exposed to NaCl solution were investigated. Corrosion in the samples was confirmed by electrochemical impedance spectroscopy (EIS). μ-XRD revealed that goethite (α-FeOOH) and akaganeite (β-FeOOH) are the main iron oxide–hydroxides formed during the chloride-induced corrosion of stainless steel in concrete. Goethite is formed closer to the surface of the steel due to the presence of chromium in the steel, while akaganeite is formed further away from the surface due to the presence of chloride ions. Detailed microstructural analysis is shown and discussed on one sample of each type of steel. - Highlights: • Synchrotron micro-diffraction used to map the distribution of crystalline phases. • Goethite and akaganeite are the main corrosion products during chloride induced corrosion in mortar. • Layers of goethite and akaganeite are negatively correlated. • EDS showed Cr present in corrosion products identified by SEM.

Spatial distribution of crystalline corrosion products formed during corrosion of stainless steel in concrete

International Nuclear Information System (INIS)

Serdar, Marijana; Meral, Cagla; Kunz, Martin; Bjegovic, Dubravka; Wenk, Hans-Rudolf; Monteiro, Paulo J.M.

2015-01-01

The mineralogy and spatial distribution of nano-crystalline corrosion products that form in the steel/concrete interface were characterized using synchrotron X-ray micro-diffraction (μ-XRD). Two types of low-nickel high-chromium reinforcing steels embedded into mortar and exposed to NaCl solution were investigated. Corrosion in the samples was confirmed by electrochemical impedance spectroscopy (EIS). μ-XRD revealed that goethite (α-FeOOH) and akaganeite (β-FeOOH) are the main iron oxide–hydroxides formed during the chloride-induced corrosion of stainless steel in concrete. Goethite is formed closer to the surface of the steel due to the presence of chromium in the steel, while akaganeite is formed further away from the surface due to the presence of chloride ions. Detailed microstructural analysis is shown and discussed on one sample of each type of steel. - Highlights: • Synchrotron micro-diffraction used to map the distribution of crystalline phases. • Goethite and akaganeite are the main corrosion products during chloride induced corrosion in mortar. • Layers of goethite and akaganeite are negatively correlated. • EDS showed Cr present in corrosion products identified by SEM

Corrosion-product transport, oxidation state and remedial measures

International Nuclear Information System (INIS)

Sawicki, J.A.; Brett, M.E.; Tapping, R.L.

1998-10-01

The issues associated with monitoring and controlling corrosion-product transport (CPT) in the balance-of-plant (BOP) and steam generators (SG) of CANDU stations are briefly reviewed. Efforts are focused on minimizing corrosion of carbon steel, which is used extensively in the CANDU primary and secondary systems. Emphasis is placed on the corrosion-product oxidation state as a monitor of water chemistry effectiveness and as a monitor of system corrosion effects. The discussion is based mostly on the results of observations from Ontario Hydro plants, and their comparisons with pressurized-water reactors. The effects of low oxygen and elevated hydrazine chemistry are reviewed, as well as the effects of layup and various startup conditions. Progress in monitoring electrochemical potential (ECP) at Ontario Hydro plants and its relationship to the oxidation state of corrosion products is reviewed. Observations on CPT on the primary side of SGs are also discussed. (author)

On the Effects of Atmospheric Particles Contamination and Humidity on Tin Corrosion

DEFF Research Database (Denmark)

D’Angelo, L.; Verdingovas, V.; Ferrero, L.

2017-01-01

The effects of hygroscopic atmospheric particles are investigated in relation to the corrosion of tin. Surface insulation resistance test boards were directly contaminated both with ambient particles sampled in the field at Milan, Italy, and with pure saline particles generated in the laboratory....... An innovative particle deposition device was used to uniformly coat circular spots on to the test board surfaces. Deliquescence and crystallization of the water-soluble compounds were detected by observing the impedance response to varying relative humidity (RH) conditions with a gradual and continuous ramps....... The effects of the adsorption/desorption kinetics and of the temperature on the deliquescence and crystallization RH values were also investigated. Leakage current measurements at 5-V dc highlighted the ability of atmospheric particles to promote corrosion and electrochemical migration at RH levels far below...

atmospheric corrosion of mild steel in the niger delta region of ...

African Journals Online (AJOL)

xtz

ABSTRACT. The atmospheric corrosion of Calabar, Cross River State environment has been investigated for 12 months using weight loss technique. The extent of pollution of the environment was also determined via measurements of the precipitation and air quality parameters. Apart from the suspended particulate.

Development and evaluation of an instantaneous atmospheric corrosion rate monitor

Science.gov (United States)

Mansfeld, F.; Jeanjaquet, S. L.; Kendig, M. W.; Roe, D. K.

1985-06-01

A research program was carried out in which a new instantaneous atmospheric corrosion rate monitor (ACRM) was developed and evaluated, and equipment was constructed which will allow the use of many sensors in an economical way in outdoor exposures. In the first task, the ACRM was developed and tested in flow chambers in which relative humidity and gaseous and particulate pollutant levels can be controlled. Diurnal cycles and periods of rain were simulated. The effects of aerosols were studied. A computerized system was used for collection, storage, and analysis of the electrochemical data. In the second task, a relatively inexpensive electronics system for control of the ACRM and measurement of atmospheric corrosion rates was designed and built. In the third task, calibration of deterioration rates of various metallic and nonmetallic materials with the response of the ACRMs attached to these materials was carried out under controlled environmental conditions using the system developed in the second task. A Quality Assurance project plan was prepared with inputs from the Rockwell International Environmental Monitoring and Service Center and Quality Assurance System audits were performed.

Effect of hydrogen chloride on the corrosion of an FeCrAlY alloy in simulated coal gasifier atmospheres

Energy Technology Data Exchange (ETDEWEB)

Coley, K.S.; Rhoades-Brown, J.E.; Blick, K.

1989-03-01

An iron chromium aluminium yttrium steel was exposed to a simulated coal gasifier atmosphere containing 1000 ppm and 2200 ppm hydrogen chloride at 450/sup 0/C. Increasing hydrogen chloride content was found to accelerate reaction rates, and significantly alter the microstructure and composition of the corrosion product. Tentative explanations for these results, involving vapour phase transport of metal chlorides are proposed.

Corrosion behaviors and effects of corrosion products of plasma electrolytic oxidation coated AZ31 magnesium alloy under the salt spray corrosion test

Science.gov (United States)

Wang, Yan; Huang, Zhiquan; Yan, Qin; Liu, Chen; Liu, Peng; Zhang, Yi; Guo, Changhong; Jiang, Guirong; Shen, Dejiu

2016-08-01

The effects of corrosion products on corrosion behaviors of AZ31 magnesium alloy with a plasma electrolytic oxidation (PEO) coating were investigated under the salt spray corrosion test (SSCT). The surface morphology, cross-sectional microstructure, chemical and phase compositions of the PEO coating were determined using scanning electron microscopy (SEM) equipped with energy dispersive X-ray spectroscopy (EDS) and X-ray diffraction analysis (XRD), respectively. Further, the corrosion process of the samples under the SSCT was examined in a non-aqueous electrolyte (methanol) using electrochemical impedance spectroscopy (EIS) coupled with equivalent circuit. The results show that the inner layer of the coating was destroyed firstly and the corrosion products have significant effects on the corrosion behaviors of the coating. The results above are discussed and an electrochemical corrosion model is proposed in the paper.

High temperature corrosion during biomass firing: improved understanding by depth resolved characterisation of corrosion products

DEFF Research Database (Denmark)

Okoro, Sunday Chukwudi; Montgomery, Melanie; Jappe Frandsen, Flemming

2015-01-01

changes within the near surface region (covering both the deposit and the steel surface). Such cross-section analysis was further complemented by plan view investigations (additionally involving X-ray diffraction) combined with removal of the corrosion products. Improved insights into the nature......The high temperature corrosion of an austenitic stainless steel (TP 347H FG), widely utilised as a superheater tube material in Danish power stations, was investigated to verify the corrosion mechanisms related to biomass firing. KCl coated samples were exposed isothermally to 560 degrees C...... of the corrosion products as a function of distance from the deposit surface were revealed through this comprehensive characterisation. Corrosion attack during simulated straw-firing conditions was observed to occur through both active oxidation and sulphidation mechanisms....

Influence of stripping and cooling atmospheres on surface properties and corrosion of zinc galvanizing coatings

International Nuclear Information System (INIS)

Yasakau, K.A.; Giner, I.; Vree, C.; Ozcan, O.; Grothe, R.; Oliveira, A.; Grundmeier, G.; Ferreira, M.G.S.; Zheludkevich, M.L.

2016-01-01

Highlights: • Stripping/cooling atmosphere affects surfaces chemical composition of Zn and Zn-Al-Mg galvanized coatings. • Higher peel forces of model adhesive films were obtained on zinc alloys samples prepared under nitrogen atmosphere. • Localized corrosion attack originates at grain boundaries on Zn galvanized coating. • Visible dissolution of MgZn_2 phase was observed by in situ AFM only at binary eutectics and not at ternary ones. - Abstract: In this work the influence of stripping/cooling atmospheres used after withdrawal of steel sheet from Zn or Zn-alloy melt on surface properties of Zn (Z) and Zn-Al-Mg (ZM) hot-dip galvanizing coatings has been studied. The aim was to understand how the atmosphere (composed by nitrogen (N_2) or air) affects adhesion strength to model adhesive and corrosive behaviour of the galvanized substrates. It was shown that the surface chemical composition and Volta potential of the galvanizing coatings prepared under the air or nitrogen atmosphere are strongly influenced by the atmosphere. The surface chemistry Z and ZM surfaces prepared under N_2 contained a higher content of metal atoms and a richer hydroxide density than the specimens prepared under air atmosphere as assessed by X-ray photoelectron spectroscopy (XPS). The induced differences on the microstructure of the galvanized coatings played a key role on the local corrosion induced defects as observed by means of in situ Atomic force microscopy (AFM). Peel force tests performed on the substrates coated by model adhesive films indicate a higher adhesive strength to the surfaces prepared under nitrogen atmosphere. The obtained results have been discussed in terms of the microstructure and surface chemical composition of the galvanizing coatings.

Removal of corrosion products of construction materials in heat carrier

International Nuclear Information System (INIS)

1975-01-01

A review of reported data has been made on the removal of structural material corrosion products into the heat-carrying agent of power reactors. The corrosion rate, and at the same time, removal of corrosion products into the heat-carrying agent (water) decreases with time. Thus, for example, the corrosion rate of carbon steel in boiling water at 250 deg C and O 2 concentration of 0.1 mg/1 after 3000 hr is 0.083 g/m 2 . day; after 9000 hr the corrosion rate has been reduced 2.5 times. Under static conditions the transfer rate of corrosion products into water has been smaller than in the stream and also depends on time. The corrosion rate of carbon steel under nuclear plant operating conditions is almost an order higher over that of steel Kh18N10T

Atmospheric Corrosivity at Australian and Overseas Airbases and Airports

Science.gov (United States)

2014-07-01

climatic conditions, the correlation between the GCIA and weight loss data from aluminium alloy coupons exposed in the open at 38 sites in the US...corrosivity. The test consists of an aluminium wire wrapped around a copper bolt exposed in the atmosphere for three months; the weight loss of the wire...Abbreviations/Acronyms AAC Army Aviation Centre AB Air Base ADF Australian Defence Force AFB Air Force Base Al aluminium ANGB Air National Guard Base

Simulation study on insoluble granular corrosion products deposited in PWR core

International Nuclear Information System (INIS)

Yang Xu; Zhou Tao; Ru Xiaolong; Lin Daping; Fang Xiaolu

2014-01-01

In the operation of reactor, such as fuel rods, reactor vessel internals etc. will be affected by corrosion erosion of high pressure coolant. It will produce many insoluble corrosion products. The FLUENT software is adopted to simulate insoluble granular corrosion products deposit distribution in the reactor core. The fluid phase uses the standard model to predict the flow field in the channel and forecast turbulence variation in the near-wall region. The insoluble granular corrosion products use DPM (Discrete Phase Model) to track the trajectory of the particles. The discrete phase model in FLUENT follows the Euler-Lagrange approach. The fluid phase is treated as a continuum by solving the Navier-Stokes equations, while the dispersed phase is solved by tracking a large number of particles through the calculated flow field. Through the study found, Corrosion products particles form high concentration area near the symmetry, and the entrance section of the corrosion products particles concentration is higher than export section. Corrosion products particles deposition attached on large area for the entrance of the cladding, this will change the core neutron flux distribution and the thermal conductivity of cladding material, and cause core axial offset anomaly (AOA). Corrosion products particles dot deposit in the outlet of cladding, which can lead to pitting phenomenon in a sheath. Pitting area will cause deterioration of heat transfer, destroy the cladding integrity. In view of the law of corrosion products deposition and corrosion characteristics of components in the reactor core. this paper proposes regular targeted local cleanup and other mitigation measures. (authors)

Atmospheric corrosion of metals in tropics and subtropic. 2. Corrosion resistance of different metals and alloys

International Nuclear Information System (INIS)

Strekalov, P.V.

1993-01-01

Data from 169 sources concerning corrosion of different metals, alloys and means of protection, obtained for a 30-year period (up to 1987) in different continent including Europe (Bulgaria, Spain, Italy, France, USSR); America (USA, Panama, Cuba, Venezuela, Brasil, Argentine); Africa (Nigeria, SAR); Australia, New Zeland, Papua-Newguinea, Philippines, are systemized. Actual results of full-scal atmospheric testings of iron, zinc, copper, cadmium, aluminium, tin, lead, carbon, low-alloys. Stainless steels, cast irons, halvanic coatings, copper, aluminium, nickel, titanium, magnesium alloys are presented. Data on the fracture rate can be used for creating the data base in banks on atmospheric resistance of metal materials

A modelling of the mechanisms occurring during the atmospheric corrosion of iron

International Nuclear Information System (INIS)

Marechal, L.; Perrin, S.; Hoerle, S.; Mazaudier, F.; Dillmann, P.

2004-01-01

In order to predict the long-term corrosion of metallic containers in storage conditions, a modelling of atmospheric corrosion of iron is proposed. This modelling takes into account the mechanisms which occur during the three stages of a wet-dry cycle. During the wetting stage, the reduction of lepidocrocite (g-FeOOH), a constituent of the rust layer, is considered to be the rate-limiting step of the corrosion. During the second stage of the cycle, the wet period, the reduction of dissolved oxygen on the lepidocrocite, previously reduced, is controlling the mechanism. The amount of oxidized metal depends on the quantity of reduced lepidocrocite and also on the oxygen diffusion in the electrolyte and the rust layer. At the end of the cycle, the blocking of the anodic sites is considered to describe the extinction of electrochemical corrosion during the drying. It appears that each stage of the cycle depends mainly on the chemical and morphological properties of the rust layer. (authors)

Studies on dissolution characteristics of simulated corrosion products on pressurized water reactor primary coolant loops. Pt.2: Cobalt simulated corrosion product

International Nuclear Information System (INIS)

Li Shan; Zhou Xianyu

1997-01-01

The studies on the dissolution characteristics of simulated corrosion product of cobalt on pressurized water reactor primary coolant loops in aqueous solution of citric acid, hydrogen peroxide and citric acid-hydrogen peroxide have been performed. The results show that the portion of the dissolved simulated corrosion product of cobalt in citric acid aqueous solution clearly increases with a rise in citric acid concentration and is ten times above the corresponding value of iron. The portion of the products that dissolve is the largest at pH 3.00 in the pH range of 2.33∼4.50 and at 70 degree C in the range of 60∼80 degree C. It is shown that the portion of the dissolved simulated corrosion product of cobalt in hydrogen peroxide aqueous solution is smaller than the corresponding value in citric acid, and that the portion of the dissolved simulated corrosion product of cobalt in aqueous solution of hydrogen peroxide-citric acid is larger than the corresponding value in single citric acid aqueous solution

A non-destructive test method to monitor corrosion products and corrosion-induced cracking in reinforced cement based materials

DEFF Research Database (Denmark)

Michel, Alexander; Pease, Bradley Justin; Peterova, Adela

2011-01-01

) was conducted to describe the impact of water-to-cement ratio and corrosion current density (i.e., corrosion rate) on the reinforcement corrosion process. Focus was placed, in particular on the determination of the corrosion accommodating region (CAR) and time to corrosion-induced cracking. Experimental results...... showed that x-ray attenuation measurements allow determination of the actual concentrations of corrosion products averaged through the specimen thickness. The total mass loss of steel measured by x-ray attenuation was found to be in very good agreement with the calculated mass loss obtained by Faraday......’s law. Furthermore, experimental results demonstrated that the depth of penetration of corrosion products as well as time to corrosion-induced cracking is varying for the different water-to-cement ratios and applied corrosion current densities....

Concrete Cracking Prediction Including the Filling Proportion of Strand Corrosion Products

Science.gov (United States)

Wang, Lei; Dai, Lizhao; Zhang, Xuhui; Zhang, Jianren

2016-01-01

The filling of strand corrosion products during concrete crack propagation is investigated experimentally in the present paper. The effects of stirrups on the filling of corrosion products and concrete cracking are clarified. A prediction model of crack width is developed incorporating the filling proportion of corrosion products and the twisting shape of the strand. Experimental data on cracking angle, crack width, and corrosion loss obtained from accelerated corrosion tests of concrete beams are presented. The proposed model is verified by experimental data. Results show that the filling extent of corrosion products varies with crack propagation. The rust filling extent increases with the propagating crack until a critical width. Beyond the critical width, the rust-filling extent remains stable. Using stirrups can decrease the critical crack width. Stirrups can restrict crack propagation and reduce the rust filling. The tangent of the cracking angle increases with increasing corrosion loss. The prediction of corrosion-induced crack is sensitive to the rust-filling extent. PMID:28772367

Influence of stripping and cooling atmospheres on surface properties and corrosion of zinc galvanizing coatings

Energy Technology Data Exchange (ETDEWEB)

Yasakau, K.A., E-mail: kyasakau@ua.pt [Department of Materials and Ceramic Engineering, CICECO—Aveiro Institute of Materials, University of Aveiro, 3810-193 Aveiro (Portugal); Giner, I. [Universität Paderborn, Fakultät NW—Department Chemie, Technische und Makromolekulare Chemie, Warburger Strasse 100, D-33098 Paderborn (Germany); Vree, C. [Salzgitter Mannesmann Forschung, GmbH Division Surface Technology, Eisenhüttenstrasse 99, 38239 Salzgitter (Germany); Ozcan, O.; Grothe, R. [Universität Paderborn, Fakultät NW—Department Chemie, Technische und Makromolekulare Chemie, Warburger Strasse 100, D-33098 Paderborn (Germany); Oliveira, A. [Department of Materials and Ceramic Engineering, CICECO—Aveiro Institute of Materials, University of Aveiro, 3810-193 Aveiro (Portugal); Grundmeier, G. [Universität Paderborn, Fakultät NW—Department Chemie, Technische und Makromolekulare Chemie, Warburger Strasse 100, D-33098 Paderborn (Germany); Ferreira, M.G.S. [Department of Materials and Ceramic Engineering, CICECO—Aveiro Institute of Materials, University of Aveiro, 3810-193 Aveiro (Portugal); Zheludkevich, M.L. [Department of Materials and Ceramic Engineering, CICECO—Aveiro Institute of Materials, University of Aveiro, 3810-193 Aveiro (Portugal); Department of Corrosion and Surface Technology, Institute of Materials Research Helmholtz-Zentrum Geesthacht, Max-Planck Str. 1, 21502 Geesthacht (Germany)

2016-12-15

Highlights: • Stripping/cooling atmosphere affects surfaces chemical composition of Zn and Zn-Al-Mg galvanized coatings. • Higher peel forces of model adhesive films were obtained on zinc alloys samples prepared under nitrogen atmosphere. • Localized corrosion attack originates at grain boundaries on Zn galvanized coating. • Visible dissolution of MgZn{sub 2} phase was observed by in situ AFM only at binary eutectics and not at ternary ones. - Abstract: In this work the influence of stripping/cooling atmospheres used after withdrawal of steel sheet from Zn or Zn-alloy melt on surface properties of Zn (Z) and Zn-Al-Mg (ZM) hot-dip galvanizing coatings has been studied. The aim was to understand how the atmosphere (composed by nitrogen (N{sub 2}) or air) affects adhesion strength to model adhesive and corrosive behaviour of the galvanized substrates. It was shown that the surface chemical composition and Volta potential of the galvanizing coatings prepared under the air or nitrogen atmosphere are strongly influenced by the atmosphere. The surface chemistry Z and ZM surfaces prepared under N{sub 2} contained a higher content of metal atoms and a richer hydroxide density than the specimens prepared under air atmosphere as assessed by X-ray photoelectron spectroscopy (XPS). The induced differences on the microstructure of the galvanized coatings played a key role on the local corrosion induced defects as observed by means of in situ Atomic force microscopy (AFM). Peel force tests performed on the substrates coated by model adhesive films indicate a higher adhesive strength to the surfaces prepared under nitrogen atmosphere. The obtained results have been discussed in terms of the microstructure and surface chemical composition of the galvanizing coatings.

Corrosion and anticorrosion. Industrial practice

International Nuclear Information System (INIS)

Beranger, G.; Mazille, H.

2002-01-01

This book comprises 14 chapters written with the collaboration of about 50 French experts of corrosion. It is complementary to another volume entitled 'corrosion of metals and alloys' and published by the same editor. This volume comprises two parts: part 1 presents the basic notions of corrosion phenomena, the properties of surfaces, the electrochemical properties of corrosion etc.. Part 2 describes the most frequent forms of corrosion encountered in industrial environments and corresponding to specific problems of protection: marine environment, atmospheric corrosion, galvanic corrosion, tribo-corrosion, stress corrosion etc.. The first 8 chapters (part 1) treat of the corrosion problems encountered in different industries and processes: oil and gas production, chemical industry, phosphoric acid industry, PWR-type power plants, corrosion of automobile vehicles, civil engineering and buildings, corrosion of biomaterials, non-destructive testing for the monitoring of corrosion. The other chapters (part 2) deal with anticorrosion and protective coatings and means: choice of materials, coatings and surface treatments, thick organic coatings and enamels, paints, corrosion inhibitors and cathodic protection. (J.S.)

Study of the effect of the NO{sub 2} in the atmospheric corrosion of copper; Estudio del efecto del NO{sub 2} en la corrosion atmosferica del cobre

Energy Technology Data Exchange (ETDEWEB)

Mariaca Rodriguez, Liboria

1997-12-31

Factors as the increase of the power consumption and the development of new combustion technologies, together with the increasing campaigns for the diminution of the SO{sub 2} emissions, have given rise to an increase of the relative importance of other atmospheric polluting agents, among which the nitrogen oxides occupy preponderant place. This new situation has motivated that during the last years greater attention is appearing to the effect these oxides can have on the stability of the materials. However, the results still are scarce and sometimes contradictory. With the purpose of contributing to the understanding of the effect of the NO{sub x} in the atmospheric corrosion, the investigation that is shown here was made. The effect that the NO{sub 2} has in the atmospheric corrosion of copper was studied, considering cases with and without the simultaneous presence of SO{sub 2}, with different relative humidities (RH) and temperatures of the atmospheric air. For this purpose one resorted to the simulation of atmospheres of interest by means of laboratory chambers that allowed the control of the temperature, RH and the contamination level. In each atmosphere completely clean copper coupons were exposed, and withdrawn at 7, 14, 21 and 28 days. Gravimetric analyses of gain and loss of mass and one complete characterization the corrosion products formed was made, mainly by means of X ray diffraction techniques by grazing angle (DRS), and photo electronic X ray spectroscopy (XPS or ESCA). Also, the applicability in these conditions of the electrochemical techniques of DC (RP, CP and RE) and of alternating current (EIE). From the results obtained it is worth mentioning as the more important the following ones: The corrosion of copper in atmospheres contaminated solely with NO{sub 2} depends fundamentally on the RH, not existing, as in the case of other metals, a critical RH (CRH), from which the kinetics of the corrosion process increases; all the opposite, the copper

Quantitative assessment of the effect of corrosion product buildup on occupational exposure

International Nuclear Information System (INIS)

Divine, J.R.

1982-10-01

The program was developed to provide a method for predicting occupational exposures caused by the deposition of radioactive corrosion products outside the core of the primary system of an operating power reactor. This predictive capability will be useful in forecasting total occupational doses during maintenance, inspection, decontamination, waste treatment, and disposal. In developing a reliable predictive model, a better understanding of the parameters important to corrosion product film formation, corrosion product transport, and corrosion product film removal will be developed. This understanding can lead to new concepts in reactor design to minimize the buildup and transport of radioactive corrosion products or to improve methods of operation. To achieve this goal, three objectives were established to provide: (1) criteria for acceptable coolant sampling procedures and sampling equipment that will provide data which will be used in the model development; (2) a quantitative assessment of the effect of corrosion product deposits on occupational exposure; and (3) a model which describes the influence of flow, temperature, coolant chemistry, construction materials, radiation, and other operating parameters on the transport and buildup of corrosion products

Oxidation kinetics of reaction products formed in uranium metal corrosion.

Energy Technology Data Exchange (ETDEWEB)

Totemeier, T. C.

1998-04-22

The oxidation behavior of uranium metal ZPPR fuel corrosion products in environments of Ar-4%O{sub 2} and Ar-20%O{sub 2} were studied using thermo-gravimetric analysis (TGA). These tests were performed to extend earlier work in this area specifically, to assess plate-to-plate variations in corrosion product properties and the effect of oxygen concentration on oxidation behavior. The corrosion products from two relatively severely corroded plates were similar, while the products from a relatively intact plate were not reactive. Oxygen concentration strongly affected the burning rate of reactive products, but had little effect on low-temperature oxidation rates.

Oxidation kinetics of reaction products formed in uranium metal corrosion

International Nuclear Information System (INIS)

Totemeier, T. C.

1998-01-01

The oxidation behavior of uranium metal ZPPR fuel corrosion products in environments of Ar-4%O 2 and Ar-20%O 2 were studied using thermo-gravimetric analysis (TGA). These tests were performed to extend earlier work in this area specifically, to assess plate-to-plate variations in corrosion product properties and the effect of oxygen concentration on oxidation behavior. The corrosion products from two relatively severely corroded plates were similar, while the products from a relatively intact plate were not reactive. Oxygen concentration strongly affected the burning rate of reactive products, but had little effect on low-temperature oxidation rates

Evaluation of corrosion products formed by sulfidation as inhibitors of the naphthenic corrosion of AISI-316 steel

Science.gov (United States)

Sanabria-Cala, J. A.; Montañez, N. D.; Laverde Cataño, D.; Y Peña Ballesteros, D.; Mejía, C. A.

2017-12-01

Naphthenic acids present in oil from most regions worldwide currently stand as the main responsible for the naphthenic corrosion problems, affecting the oil-refining industry. The phenomenon of sulfidation, accompanying corrosion processes brought about by naphthenic acids in high-temperature refining plant applications, takes place when the combination of sulfidic acid (H2S) with Fe forms layers of iron sulphide (FeS) on the material surface, layers with the potential to protect the material from attack by other corrosive species like naphthenic acids. This work assessed corrosion products formed by sulfidation as inhibitors of naphthenic corrosion rate in AISI-316 steel exposed to processing conditions of simulated crude oil in a dynamic autoclave. Calculation of the sulfidation and naphthenic corrosion rates were determined by gravimetry. The surfaces of the AISI-316 gravimetric coupons exposed to acid systems; were characterized morphologically by X-Ray Diffraction (XRD) and X-ray Fluorescence by Energy Dispersive Spectroscopy (EDS) combined with Scanning Electron Microscopy (SEM). One of the results obtained was the determination of an inhibiting effect of corrosion products at 250 and 300°C, where lower corrosion rate levels were detected. For the temperature of 350°C, naphthenic corrosion rates increased due to deposition of naphthenic acids on the areas where corrosion products formed by sulfidation have lower homogeneity and stability on the surface, thus accelerating the destruction of AISI-316 steel. The above provides an initial contribution to oil industry in search of new alternatives to corrosion control by the attack of naphthenic acids, from the formation of FeS layers on exposed materials in the processing of heavy crude oils with high sulphur content.

Bearing assembly and the like for use in corrosive and non-corrosive atmospheres

International Nuclear Information System (INIS)

Mashburn, D.N.; Woodall, H.C.; Wright, R.R.

1979-01-01

This invention relates to a novel machine element characterized by mutually rubbing surfaces which are composed of dissimilar materials having high hardness, a low coefficient of friction, and resistance to corrosion by halogen-containing atmospheres. As exemplified by the preferred embodiment for use in gaseous UF 6 , the rubbing surfaces are chemically deposited nickel and anodized aluminum. These surfaces permit jam-free operation despite long-term exposure to UF 6 . Preferably, both surfaces have a hardness of at least about 500 HV 100 on the Vickers hardness scale, and preferably the anodized-aluminum surface is of type having comparatively little tendency to sorb uranium hexafluoride

A process for the production of a scale-proof and corrosion-resistant coating on graphite and carbon bodies

Science.gov (United States)

Fitzer, E.

1981-01-01

A process for the production of a corrosion resistant coating on graphite and carbon bodies is described. The carbon or graphite body is coated or impregnated with titanium silicide under the addition of a metal containing wetting agent in a nitrogen free atmosphere, so that a tight coating is formed.

Deposition of corrosion products in-core

International Nuclear Information System (INIS)

Burrill, K.A.

1994-11-01

Data on corrosion product deposits on fuel sheaths are presented for a variety of operating conditions and water chemistries: boiling and non-boiling water; surface heat flux; pH, dissolved hydrogen concentration. Corrosion product behaviour in-core may be interpreted in terms of the solubility of magnetite and how it changes with water chemistry and temperature. A hypothesis of the deposition and release mechanisms was proposed in the 1970s in which particles deposited onto the sheath and subsequently dissolved in the heated water while being irradiated. Some of the deposition data may be interpreted using a model of these mechanisms. (author). 5 refs., 6 tabs., 8 figs

New Insights in the Long-Term Atmospheric Corrosion Mechanisms of Low Alloy Steel Reinforcements of Cultural Heritage Buildings

Directory of Open Access Journals (Sweden)

Marie Bouchar

2017-06-01

Full Text Available Reinforcing clamps made of low alloy steel from the Metz cathedral and corroded outdoors during 500 years were studied by OM, FESEM/EDS, and micro-Raman spectroscopy. The corrosion product layer is constituted of a dual structure. The outer layer is mainly constituted of goethite and lepidocrocite embedding exogenous elements such as Ca and P. The inner layer is mainly constituted of ferrihydrite. The behaviour of the inner layer under conditions simulating the wetting stage of the RH wet/dry atmospheric corrosion cycle was observed by in situ micro-Raman spectroscopy. The disappearance of ferrihydrite near the metal/oxide interface strongly suggests a mechanism of reductive dissolution caused by the oxidation of the metallic substrate and was observed for the first time in situ on an archaeological system.

Effects of Si as alloying element on corrosion resistance of weathering steel

International Nuclear Information System (INIS)

Mejía Gómez, J.A.; Antonissen, J.; Palacio, C.A.; De Grave, E.

2012-01-01

Highlights: ► Weathering steels with different concentrations of Si as alloying element were exposed to laboratory atmospheric conditions. ► The iron oxides formed as corrosion products were characterized and analyzed by XRD, TEM and Mössbauer spectroscopy. ► Silicon affects the corrosion resistance of weathering steels. ► Silicon promotes the formation of goethite as corrosion product with small particle size. - Abstract: The corrosion resistance in saline conditions of weathering steel with different concentrations of Si (1, 2 and 3 wt.%) exposed to dip dry tests (simulating wet/dry cycles of atmospheric corrosion) was studied by weight loss, X-ray diffraction, Mössbauer spectroscopy and transmission electron microscopy. The results showed that the steels exhibit better corrosion performance with increasing Si concentration. The formation of Fe-oxides such as goethite, lepidocrocite and magnetite was observed. Superparamagnetic goethite is the dominant phase in the rust developed on the Si steels, indicating that Si favors the formation of goethite with small particle size.

Quantifying movements of corrosion products in reinforced concrete using x-ray attenuation measurements

DEFF Research Database (Denmark)

Pease, Bradley Justin; Michel, Alexander; Stang, Henrik

2011-01-01

Corrosion of steel reinforcement, embedded in concrete, may substantially degrade concrete structures due to the expansive nature of corrosion products. Expansion of corrosion products cause tensile stresses to develop and cracks to form in concrete. Extensive research has focused on corrosion...... of corrosion products move into the concrete without generating tensile stresses and cracks in the concrete. Typically, corrosion products are thought to occupy pores, interfacial defects, and/or air voids located near the concrete-steel interface and stresses develop only after filling of these pores. Further....... X-ray attenuation measurements are also capable of detecting cracks. Therefore, this approach provides a direct measurement of the amount and location of reinforcement corrosion products required to induce cracking. Results of a parametric investigation on the impact of water-to-cement ratio (0...

Corrosion products study of alcohol by Mossbauer spectroscopy

International Nuclear Information System (INIS)

Velazquez, R.; Gil de Larre, M.

1995-01-01

Simulated corrosion essays in alcohol is presented and corrosion products of storage tanks (CAPASA) were analyzed. The analysis by Mossbauer absortion and transmission spectroscopy shows the formation of hematite substratum in the rust of the storage tanks of carburetant and burning alcohol. In the sample of corrosion with strong rum shows the formation of lepidocrocite and with destilled water besides of lepidocrocite, magnetite (Fe3 O4) is detected

Influence of stripping and cooling atmospheres on surface properties and corrosion of zinc galvanizing coatings

Science.gov (United States)

Yasakau, K. A.; Giner, I.; Vree, C.; Ozcan, O.; Grothe, R.; Oliveira, A.; Grundmeier, G.; Ferreira, M. G. S.; Zheludkevich, M. L.

2016-12-01

In this work the influence of stripping/cooling atmospheres used after withdrawal of steel sheet from Zn or Zn-alloy melt on surface properties of Zn (Z) and Zn-Al-Mg (ZM) hot-dip galvanizing coatings has been studied. The aim was to understand how the atmosphere (composed by nitrogen (N2) or air) affects adhesion strength to model adhesive and corrosive behaviour of the galvanized substrates. It was shown that the surface chemical composition and Volta potential of the galvanizing coatings prepared under the air or nitrogen atmosphere are strongly influenced by the atmosphere. The surface chemistry Z and ZM surfaces prepared under N2 contained a higher content of metal atoms and a richer hydroxide density than the specimens prepared under air atmosphere as assessed by X-ray photoelectron spectroscopy (XPS). The induced differences on the microstructure of the galvanized coatings played a key role on the local corrosion induced defects as observed by means of in situ Atomic force microscopy (AFM). Peel force tests performed on the substrates coated by model adhesive films indicate a higher adhesive strength to the surfaces prepared under nitrogen atmosphere. The obtained results have been discussed in terms of the microstructure and surface chemical composition of the galvanizing coatings.

Inhibition treatment of the corrosion of lead artefacts in atmospheric conditions and by acetic acid vapour: use of sodium decanoate

International Nuclear Information System (INIS)

Rocca, E.; Rapin, C.; Mirambet, F.

2004-01-01

The efficiency of linear sodium decanoate, CH 3 (CH 2 ) 8 COONa (noted NaC 10 ), as corrosion inhibitor of lead was determined by electrochemical techniques in two corrosive mediums: ASTM D1384 standard water and acetic acid-enriched solutions. Best results were obtained with 0.05 mol l -1 of NaC 10 solution. In these conditions, the inhibition efficiency can be estimated of 99.9%. The corrosion inhibition effect was confirmed by cyclic atmospheric tests in a climatic chamber in two different conditions: water saturated vapour, and acid acetic enriched vapour simulating the atmosphere in the wooden displays in museums. Surface analyses by SEM and X-ray diffraction indicate that the metal protection is due to the formation of a protective layer mainly composed of lead decanoate Pb(C 10 ) 2 (metallic soap). This inhibition treatment was applied on objects of metallic cultural heritage: gallo-roman sarcophagus in lead. Electrochemical methods confirm the efficiency of treatment on archaeological materials. In conclusion, this inhibitor treatment seems to be very promising against the atmospheric corrosion and the corrosion by organic acid vapour in museums

Corrosion and protection of metals in the rural atmosphere of El Pardo Spain (PATINA/CYTED project)

International Nuclear Information System (INIS)

Simancas, J.; Castano, J. G.; Morcillo, M.

2003-01-01

Atmospheric corrosion tests of metallic and organic coatings on steel, zinc and aluminium have been conducted in el Pardo (Spain) as part of the PATINA/CYTED project Anticorrosive Protection of Metals in the Atmosphere. This is a rural atmosphere with the following ISO corrosivity categories: C2 (Fe), C'' (Zn), Cu (Cu) and C1 (Al). Its average temperature and relative humidity is 13 degree centigrade and 62.8, respectively, and it has low SO 2 and C1''- contents. Results of 42 months exposure are discussed. Atmospheric exposure tests were carried out for the following types of coatings: conventional paint coatings for steel and hot-dip galvanized steel (group 1), new painting technologies for steel and galvanized steel (group 2), zinc-base metallic coatings (group 3), aluminium-base metallic coatings (group 4), coatings on aluminium (group 5) and coil-coatings on steel, hot-dip galvanized steel and 55% Al-Zn coated steel (group 6). (Author) 9 refs

Corrosion products of reinforcement in concrete in marine and industrial environments

International Nuclear Information System (INIS)

Vera, R.; Villarroel, M.; Carvajal, A.M.; Vera, E.; Ortiz, C.

2009-01-01

The corrosion products formed on embedded steel in concrete under simulated marine and industrial conditions and natural marine environment were studied. A 0.50 water/cement ratio concrete was used and 3.5% NaCl and 180 g L -1 of H 2 SO 4 with 70 ppm of chloride ions solutions were used to simulate the synthetic medium. The initial electrochemical variables of the steel and pH, chlorides and sulfates profiles were measured according to the concrete depth. The morphology of the corrosive attack was determined via scanning electron microscopy (SEM), and the composition of the corrosion products was determined using an X-ray analyzer and an X-ray diffractometer (XRD). The protective power of the corrosion products was evaluated through anodic polarization curves in a saturated Ca(OH) 2 solution. The results from XRD and SEM show that all the resulting corrosion products correspond to lepidocrocite, goethite and magnetite mixtures; moreover, akaganeite was also identified under natural and simulated marine environments. Siderite was only detected in samples exposed to a natural marine environment. Concerning the protective nature of the corrosion products, these show lower performance in a simulated industrial environment, where the corrosion rate of the steel is up to 1.48 μm year -1

Corrosion products of reinforcement in concrete in marine and industrial environments

Energy Technology Data Exchange (ETDEWEB)

Vera, R. [Instituto de Quimica, Facultad de Ciencias, Pontificia Universidad Catolica de Valparaiso, Avenida Brasil 2950, Casilla 4059, Valparaiso (Chile)], E-mail: rvera@ucv.cl; Villarroel, M. [Instituto de Quimica, Facultad de Ciencias, Pontificia Universidad Catolica de Valparaiso, Avenida Brasil 2950, Casilla 4059, Valparaiso (Chile); Carvajal, A.M. [Facultad de Ingenieria, Escuela de Construccion Civil, Pontificia Universidad Catolica de Chile, Av. Vicuna Mackenna 4860, Macul, Santiago (Chile); Vera, E.; Ortiz, C. [Universidad Pedagogica y Tecnologica de Colombia, Avenida Central Norte, Km 2, Tunja (Colombia)

2009-03-15

The corrosion products formed on embedded steel in concrete under simulated marine and industrial conditions and natural marine environment were studied. A 0.50 water/cement ratio concrete was used and 3.5% NaCl and 180 g L{sup -1} of H{sub 2}SO{sub 4} with 70 ppm of chloride ions solutions were used to simulate the synthetic medium. The initial electrochemical variables of the steel and pH, chlorides and sulfates profiles were measured according to the concrete depth. The morphology of the corrosive attack was determined via scanning electron microscopy (SEM), and the composition of the corrosion products was determined using an X-ray analyzer and an X-ray diffractometer (XRD). The protective power of the corrosion products was evaluated through anodic polarization curves in a saturated Ca(OH){sub 2} solution. The results from XRD and SEM show that all the resulting corrosion products correspond to lepidocrocite, goethite and magnetite mixtures; moreover, akaganeite was also identified under natural and simulated marine environments. Siderite was only detected in samples exposed to a natural marine environment. Concerning the protective nature of the corrosion products, these show lower performance in a simulated industrial environment, where the corrosion rate of the steel is up to 1.48 {mu}m year{sup -1}.

The anaerobic corrosion of carbon steel in concrete

International Nuclear Information System (INIS)

Naish, C.C.; Balkwill, P.H.; O'Brien, T.M.; Taylor, K.J.; Marsh, G.P.

1990-11-01

The report describes the work of a two year programme investigating the anaerobic corrosion of carbon steel embedded in a range of candidate repository cements and concretes at laboratory ambient temperatures. The factors investigated in the study were the rate of the anaerobic corrosion reaction, the effect of hydrogen overpressure on the reaction rate and the form of the corrosion product. Both electrochemical and sample weight loss corrosion rate measurements were used. The cements and concretes used were prepared both with and without small additions of chloride (2% by weight of mix water). The results indicate that the corrosion rate is low, <1 μm/year, the effect of hydrogen overpressure is not significant over the range of pressures investigated, 1-100 atmospheres, and that the corrosion product is dependent on the cement used to cast the samples. Magnetite was identified in the case of blast furnace slag replacement cements but for pulverised fuel ash and ordinary Portland cements no corrosion product was evident either from X-ray diffraction or laser Raman measurements. (Author)

High temperature corrosion in chloridizing atmospheres: development of material quasi-stability diagrams and coatings

Energy Technology Data Exchange (ETDEWEB)

Doublet, S.; Schuetze, M. [Karl-Winnacker-Institut der DECHEMA e.V., Theodor-Heuss-Allee 25, D-60486 Frankfurt am Main (Germany)

2004-07-01

Chlorine gas is widely encountered in chemical industries, e. g. in waste incinerators and plastic/polymer decomposition mills. The presence of chlorine may significantly reduce the life-time of the components. Although metallic materials have been widely used under such conditions there is still a need for data on the role of the different alloying elements in commercial alloys. The purpose of this work is to produce a clear picture of which alloying elements play a detrimental role and which elements are beneficial. These results can be used as a tool for general assessment of metallic alloys with regard to their performance in chloridizing high temperature environments. A previous study has already been performed in oxidizing-chloridizing atmospheres and led to the elaboration of material quasi-stability diagrams. As a follow-up the present work has been performed in reducing-chloridizing atmospheres in order to validate these diagrams at low partial pressures of oxygen. The behaviour of 9 commercial materials where the content of the major alloying elements was varied in a systematic manner was investigated in reducing-chloridizing atmospheres (in Ar containing up to 2 vol.% Cl{sub 2} and down to 1 ppm O{sub 2}) at 800 deg. C. As the thermodynamical approach to corrosion in such atmospheres could not explain all the phenomena which occur, kinetics calculations i.e. diffusion calculations were carried out. Pack cementation and High Velocity Oxy-Fuel (HVOF) coatings were also developed from the best alloying elements previously found by the calculations and the corrosion experiments. Corrosion tests on the coated materials were then performed in the same conditions as the commercial alloys. (authors)

Characterisation of corrosion products on pipeline steel under cathodic protection

Energy Technology Data Exchange (ETDEWEB)

Lanarde, Lise [Gaz de France Research and Development Division, 361 avenue du President Wilson, BP33, 93211 Saint Denis La Plaine (France)]|[UPR15 du CNRS, Laboratoire des Interfaces et Systemes Electrochimiques, Universite Pierre et Marie Curie, C.P. 133, 4 Place Jussieu, 75252 Paris Cedex 05 (France); Campaignolle, Xavier; Karcher, Sebastien; Meyer, Michel [Gaz de France Research and Development Division, 361 avenue du President Wilson, BP33, 93211 Saint Denis La Plaine (France); Joiret, Suzanne [UPR15 du CNRS, Laboratoire des Interfaces et Systemes Electrochimiques, Universite Pierre et Marie Curie, C.P. 133, 4 Place Jussieu 75252 Paris Cedex 05 (France)

2004-07-01

Onshore gas transmission lines are conjointly protected against external corrosion by cathodic protection (CP) and organic coatings. If both protection systems are simultaneously faulty, the pipe may be subjected to local loss of protection criteria. Consequently, the development of a corrosion due to the ground intrinsic corrosiveness may occur. To guarantee an optimal and safe use of its 31000 km buried gas transmission network, Gaz de France regularly inspects its pipelines. When indications of metal damage are suspected, excavations are realized to carry out a finer diagnosis and, if necessary, to repair. Whenever, corrosions are encountered, although it occurs very scarcely, it is necessary to evaluate its degree of gravity: activity, mechanism, and kinetics. Among corrosion defects, it is indeed essential to differentiate those active, from those older inactive at the time of excavation, since those last ones may possibly have been annihilated, by a PC reinforcement for instance. Eventually, the identification of the corrosion mechanism and its associated rate will provide an assessment of the risks encountered by other sections of the pipeline similar to that excavated. This study investigates to what extent the degree of gravity (activity, kinetics) of a corrosion can be determined by the characterization and identification of its associated corrosion products. Moreover, it will attempt to relate it to the close environment features as well as to the operating conditions of the pipe. The preliminary results presented in this paper consist in a laboratory study of the time evolution of corrosion products formed on the surface of ordinary low carbon steel samples. The specimens have been previously subjected to various polarization conditions in various aqueous media. The selected solutions are characteristic of ground waters. The main parameters considered for the definition of the media were its initial chemical composition, pH and dissolved gas composition

Effect of high temperature filtration on out-core corrosion product activity

International Nuclear Information System (INIS)

Horvath, G.L.; Bogancs, J.

1983-01-01

Investigation of the effect of high temperature filtration on corrosion product transport and out-core corrosion product activity has been carried out for VVER-440 plants. In the physico-chemical model applied particulate and dissolved corrosion products were taken into account. We supposed 100% effectivity for the particulate filter. It was found that about 0,5% 160 t/h/ of the main flow would result in an approx.50% reduction of the out-core corrosion product activity. Investigation of the details of the physico-chemical model in Nuclear Power Plant Paks showed a particle deposition rate measured during power transients fairly agreeing with other measurements and data used in the calculations. (author)

Corrosion Testing Facility

Data.gov (United States)

Federal Laboratory Consortium — The Corrosion Testing Facility is part of the Army Corrosion Office (ACO). It is a fully functional atmospheric exposure site, called the Corrosion Instrumented Test...

The anaerobic corrosion of carbon steel in concrete

International Nuclear Information System (INIS)

Naish, C.C.; Balkwill, P.H.; O'Brien, T.M.; Taylor, K.J.; Marsh, G.P.

1990-11-01

The report describes the work of a two year programme investigating the anaerobic corrosion of carbon steel embedded in a range of candidate repository cements and concretes at laboratory temperatures. The factors investigated in the study were the rate of the anaerobic corrosion reaction, the effect of hydrogen overpressure on the reaction rate and the form of the corrosion product. Both electrochemical and sample weight loss corrosion rate measurements were used. The cements and concretes used were prepared both with and without small additions of chloride (2% by weight of mix water). The results indicate that the corrosion rate is low, < 1 μm/year, the effect of hydrogen overpressure is not significant over the range of pressures investigated, 1-100 atmospheres, and that the corrosion product is dependent on the cement used to cast the samples. Magnetite was identified in the case of blast furnace slag replacement cements but for pulverised fuel ash and ordinary Portland cements no corrosion product was evident either from X-ray diffraction or laser Raman measurements. Further work is presently underway to investigate the effects of elevated temperatures and chloride levels on the anaerobic corrosion reaction and the rate of hydrogen gas production. (author)

Modeling of atmospheric corrosion environments and its application to constant dew-point corrosion test; Yagai taiki fushoku kankyo no modeling to sore ni motozuku teirotengata saikuru fushoku shikenho no kaihatsu

Energy Technology Data Exchange (ETDEWEB)

Muto, I. [Nippon Steel Corp., Tokyo (Japan)] Sugimoto, K. [Tohoku Univ., Sendai (Japan)

1998-08-15

Recently, stainless steel is increasing its demand for corrosion resistant building materials. Then, as it is necessary to develop and accelerating testing method capable of accurately estimating weatherability at sea side area, such testing method has no been developed yet because of difficulty to quantify corrosive environment relating to atmospheric corrosion phenomenon. As air temperature and relative humidity in outdoor change in complex, specific temperature and relative humidity cannot be used for their representative values. And, construction of corrosive factors such as sea salt particles, and so on are also much different at each area. However, at coastal area, a dew water dissolving the sea salt particles, so called droplets of chlorides aqueous solution is formed onto material surface. Then, in this study, on a base of drying and humidity absorption behavior and daily change behavior of temperature and humidity in outdoor, modeling of atmospheric corrosion environment was tried. An accelerating testing method according to this modeling was developed, long-term weathering test was compared with the corrosion behavior of the same steel, and validity of a new accelerating testing method was evaluated. 22 refs., 12 figs., 2 tabs.

A study of the evolution of rust on Mo–Cu-bearing fire-resistant steel submitted to simulated atmospheric corrosion

International Nuclear Information System (INIS)

Hao Long; Zhang Sixun; Dong Junhua; Ke Wei

2012-01-01

Highlights: ► The rusting evolution of a Mo–Cu-bearing fire-resistant steel in a simulated industrial atmosphere was investigated. ► The rusting evolution of the steel is related to the rust composition, structure, and electrochemical characteristics. ► Increased content of α-FeOOH and decreased γ-FeOOH and Fe 3 O 4 indicate the enhanced resistance of the rust. ► Mo and Cu are involved in the formation of molybdate and Cu(I)-bearing compounds in the rust. - Abstract: The corrosion evolution of a Mo–Cu-bearing fire-resistant steel in a simulated industrial atmosphere was investigated by corrosion weight gain, XRD, EPMA, XPS, and polarization curves. The results indicate that the corrosion kinetics is closely related to the rust composition and electrochemical properties. As the corrosion proceeds, the relative content of γ-FeOOH and Fe 3 O 4 decreases and α-FeOOH increases, and the rust layer becomes compact and adherent to steel substrate. Molybdenum and copper enrich in the inner rust layer, especially at the bottom of the corrosion nest, forming non-soluble molybdate and Cu(I)-bearing compounds responsible for enhanced corrosion resistance of the rust layer.

XPS and Auger investigation of mechanisms affecting corrosion inhibition of metals

International Nuclear Information System (INIS)

Holmes, R.M.; Surman, D.J.

1989-01-01

Atmospheric corrosion of metal surfaces need not be extremely obvious to cause extensive damage to many products. Very small corrosion pits and spots can cause defects in critical copper sources, often resulting in the catastrophic failure of complete electronic assemblies. Microscopic corrosion in steel can lead to the complete failure of subsequently added coatings or furnishings, the automotive industry has become aware. In addition, corrosion at its earliest stages can initiate other corrosion at a later date, resulting in inferior finishings or coatings. A major interest in atmospheric corrosion is in the mechanism by which the initial corrosion initiated and propagated. The initial phase involves the attack of the very other surface layers, hence it is difficult to observe with conventional techniques such as SEM/EDX. This paper presents some of the results obtained by both Auger electron spectroscopy and x- ray photoelectron spectroscopy, of steel and copper samples exposed to corrosive materials under controlled conditions

Corrosion mechanism of model zinc-magnesium alloys in atmospheric conditions

International Nuclear Information System (INIS)

Prosek, T.; Nazarov, A.; Bexell, U.; Thierry, D.; Serak, J.

2008-01-01

Recently, superior corrosion properties of zinc coatings alloyed with magnesium have been reported. Corrosion behaviour of model zinc-magnesium alloys was studied to understand better the protective mechanism of magnesium in zinc. Alloys containing from 1 to 32 wt.% magnesium, pure zinc, and pure magnesium were contaminated with sodium chloride and exposed to humid air for 28 days. Composition of corrosion products was analyzed using infrared spectroscopy (FTIR), ion chromatography (IC), and Auger electron spectroscopy (AES). The exposure tests were completed with scanning Kelvin probe (SKP) and electrochemical measurements. Weight loss of ZnMg alloys with 1-16 wt.% magnesium was lower than that of pure zinc. Up to 10-fold drop in weight loss was found for materials with 4-8 wt.% Mg in the structure. The improved corrosion stability of ZnMg alloys was connected to the presence of an Mg-based film adjacent to the metal surface. It ensured stable passivity in chloride environment and limited the efficiency of oxygen reduction

Atmospheric corrosion Monitoring with Time-of-Wetness (TOW) sensor and Thin Film Electric Resistance (TFER) sensor

International Nuclear Information System (INIS)

Jung, Sung Won; Kim, Young Geun; Song, Hong Seok; Lee, Seung Min; Kho, Young Tai

2002-01-01

In this study, TOW sensor was fabricated with the same P. J. Serada's in NRC and was evaluated according to pollutant amount and wet/dry cycle. Laboratorily fabricated thin film electric resistance (TFER) probes were applied in same environment for the measurement of corrosion rate for feasibility. TOW sensor could not differentiate the wet and dry time especially at polluted environment like 3.5% NaCl solution. This implies that wet/dry time monitoring by means of TOW sensor need careful application on various environment. TFER sensor could produce instant atmospheric corrosion rate regardless of environment condition. And corrosion rate obtained by TFER sensor could be differentiated according to wet/dry cycle, wet/dry cycle time variation and solution chemistry. Corrosion behaviors of TFER sensor showed that corrosion could proceed even after wet cycle because of remained electrolyte at the surface

Corrosion products in the primary circuits of PWRs

International Nuclear Information System (INIS)

Darras, R.

1983-01-01

The characteristics of PWR primary circuits are recalled, particularly the chemical specifications of the medium and the various materials used (austenitic steel, nickel alloys, cobalt-based alloys and zirconium alloys). The behaviour of these materials as regards general corrosion in nominal and transient conditions is then outlined briefly, special emphasis being laid on the effect of the determining parameters on the quantity of corrosion products formed. The release of the latter into the primary coolant is caused by two main processes: solubilization and erosion. Particular attention was given therefore to the laws governing the solubility of the oxides involved, especially as a function of temperature and pH. Erosion, or release in the form of solid particles, is relatively severe during transient events. As these corrosion products are then carried through all circuits, they cause deposits to form in favourable places on the walls as a result either of precipitation of soluble species or of sedimentation followed by consolidation of suspended particles. The presence of corrosion products in the primary circuits creates a particular impact since they become radioactive as they pass through the core and especially when they remain in it in the form of deposits; as a result, the products are capable of contaminating the entire system. Finally, although long-term reliability is obviously an essential condition for materials developed, attention must also be given to problems associated with a build-up of corrosion products in the cooling circuits and efforts made to minimize them. To that end, a number of precautions are recommended, and various remedies can be applied: selecting materials which are not readily activated, keeping structures clean, purifying fluids properly, restricting solubilization and precipitation, and perhaps, periodic decontamination. (author)

IN DRIFT CORROSION PRODUCTS

Energy Technology Data Exchange (ETDEWEB)

D.M. Jolley

1999-12-02

As directed by a written development plan (CRWMS M&O 1999a), a conceptual model for steel and corrosion products in the engineered barrier system (EBS) is to be developed. The purpose of this conceptual model is to assist Performance Assessment Operations (PAO) and its Engineered Barrier Performance Department in modeling the geochemical environment within a repository drift, thus allowing PAO to provide a more detailed and complete in-drift geochemical model abstraction and to answer the key technical issues (KTI) raised in the NRC Issue Resolution Status Report (IRSR) for the Evolution of the Near-Field Environment (NFE) Revision 2 (NRC 1999). This document provides the conceptual framework for the in-drift corrosion products sub-model to be used in subsequent PAO analyses including the EBS physical and chemical model abstraction effort. This model has been developed to serve as a basis for the in-drift geochemical analyses performed by PAO. However, the concepts discussed within this report may also apply to some near and far-field geochemical processes and may have conceptual application within the unsaturated zone (UZ) and saturated zone (SZ) transport modeling efforts.

Evolutionary Computation Techniques for Predicting Atmospheric Corrosion

Directory of Open Access Journals (Sweden)

Amine Marref

2013-01-01

Full Text Available Corrosion occurs in many engineering structures such as bridges, pipelines, and refineries and leads to the destruction of materials in a gradual manner and thus shortening their lifespan. It is therefore crucial to assess the structural integrity of engineering structures which are approaching or exceeding their designed lifespan in order to ensure their correct functioning, for example, carrying ability and safety. An understanding of corrosion and an ability to predict corrosion rate of a material in a particular environment plays a vital role in evaluating the residual life of the material. In this paper we investigate the use of genetic programming and genetic algorithms in the derivation of corrosion-rate expressions for steel and zinc. Genetic programming is used to automatically evolve corrosion-rate expressions while a genetic algorithm is used to evolve the parameters of an already engineered corrosion-rate expression. We show that both evolutionary techniques yield corrosion-rate expressions that have good accuracy.

A mini-catalogue of metal corrosion products studied by Raman microscopy

International Nuclear Information System (INIS)

Bouchard, M.; Smith, D.C.

2000-01-01

Full text.The extensive development of physical methods of analysis since the beginning of this century has revolutionised the classical observation techniques most frequently used by the archaeologist. Raman Microscopy (RM) appears to be one of the most promising tools due to the many advantages that it offers: e.g. non-destructive, in situ, micro-analysis. RM is being applied to many archaeological fields as well as to industrial or environmental sectors. In relation with parallel studies made on the identification of corrosion products on archaeological materials, and according to the principal condition for the RM characterisation of an unknown product being the comparison of its Raman spectrum with known standard spectra, the essential aim of this study is to build a mini-catalogue of standard corrosion products susceptible to be found on metallic objects; these could be from archaeological as well as from modern contexts. However, it is noted that the identification of a corrosion product may suggest either an urgent intervention from the restoration team (in the case of active corrosion products), or a stabilisation of the corrosion layer if this is considered to be a protective layer. All the standard samples are natural minerals coming from the Museum National d'Histoire Naturelle in Paris (France) and correspond to the corrosion products most frequently found on metals such copper, zinc, lead or tin. These samples have been analyzed by RM and also confirmed by powder x-ray diffraction analysis. This catalogue, including more than 30 standard species corresponding to the most common metal corrosion products, is very useful for the different studies in progress in collaboration with different archaeological metal restoration teams. The near future will probably see a mobile Raman Microprobe (MRM) equipped with many different mini-catalogues on the site of a corroded mettalic bridge, a corroded canalisation or under the sea to rapidly identify the different

GCR dismantling: corrosion of vessel internals during decay storage

International Nuclear Information System (INIS)

Gras, J.M.

1991-06-01

Gas-cooled reactor decommissioning confronts EDF with the problem of the corrosion resistance of vessel internals over a decay storage period fixed at 50 years. The layer of magnetite previously formed in the C0 2 should protect structural steelwork from atmospheric corrosion. In any case, estimated steel corrosion after 50 years may be put at below or equal to 0.1 mm and the corresponding swelling induced by corrosion products at 0.2 mm. There should be no risk of hydrogen embrittlement or stress corrosion cracking of threaded fasteners. Corrosion tests aimed at providing further insight into the effects of the magnetite layer and a program for the surveillance of post-decommissioning structural corrosion should nevertheless be envisaged

The effect of zinc addition on PWR corrosion product deposition on zircaloy-4

International Nuclear Information System (INIS)

Walters, W.S.; Page, J.D.; Gaffka, A.P.; Kingsbury, A.F.; Foster, J.; Anderson, A.; Wickenden, D.; Henshaw, J.; Zmitko, M.; Masarik, V.; Svarc, V.

2002-01-01

During the period 1995 to 2001 a programme of loop irradiation tests have been performed to confirm the effectiveness of zinc additions on PWR circuit chemistry and corrosion. The programme included two loop irradiation experiments, and subsequent PIE; the experiments were a baseline test (no added zinc) and a test with added zinc (10 ppb). This paper addresses the findings regarding corrosion product deposition and activation on irradiated Zircaloy-4 surfaces. The findings are relevant to overall corrosion of the reactor primary circuit, the use of zinc as a corrosion inhibitor, and activation and transport of corrosion products. The irradiation experience provides information on the equilibration of the loop chemistry, with deliberate injection of zinc. The PIE used novel and innovative techniques (described below) to obtain samples of the oxide from the irradiated Zircaloy. The results of the PIE, under normal chemistry and zinc chemistry, indicate the effect of zinc on the deposition and activation of corrosion products on Zircaloy. It was found that corrosion product deposition on Zircaloy is enhanced by the addition of zinc (but corrosion product deposition on other materials was reduced in the presence of zinc). Chemical analysis and radioisotope gamma counting results are presented, to interpret the findings. A computer model has also been used to simulate the corrosion product deposition and activation, to assist in the interpretation of the results. (authors)

TEM characterization of corrosion products formed on a SS-15ZR alloy

International Nuclear Information System (INIS)

Luo, J. S.; Abraham, D. P.

2000-01-01

The corrosion products formed on a stainless steel-15Zr (SS-15Zr) alloy have been characterized by transmission electron microscopy (TEM) and energy dispersive x-ray spectroscopy (EDS). Examination of alloy particles that were immersed in 90 C deionized water for two years revealed that different corrosion products were formed on the stainless steel and intermetallic phases. Two corrosion products were identified on an austenite particle: trevorite (NiFe 2 O 4 ) in the layer close to the metal and maghemite (Fe 2 O 3 ) in the outer layer. The corrosion layer formed on the intermetallic was uniform, adherent, and amorphous. The EDS analysis indicated that the layer was enriched in zirconium when compared with the intermetallic composition. High-resolution TEM images of the intermetallic-corrosion layer interface show an interlocking metal-oxide interface which may explain the relatively strong adherence of the corrosion layer to the intermetallic surface. These results will be used to evaluate corrosion mechanisms and predict long-term corrosion behavior of the alloy waste form

Nuclear reactor structural material forming less radioactive corrosion product

International Nuclear Information System (INIS)

Nakazawa, Hiroshi.

1988-01-01

Purpose: To provide nuclear reactor structural materials forming less radioactive corrosion products. Constitution: Ni-based alloys such as inconel alloy 718, 600 or inconel alloy 750 and 690 having excellent corrosion resistance and mechanical property even in coolants at high temperature and high pressure have generally been used as nuclear reactor structural materials. However, even such materials yield corrosion products being attacked by coolants circulating in the nuclear reactor, which produce by neutron irradiation radioactive corrosion products, that are deposited in primary circuit pipeways to constitute exposure sources. The present invention dissolves dissolves this problems by providing less activating nuclear reactor structural materials. That is, taking notice on the fact that Ni-58 contained generally by 68 % in Ni changes into Co-58 under irradiation of neutron thereby causing activation, the surface of nuclear reactor structural materials is applied with Ni plating by using Ni with a reduced content of Ni-58 isotopes. Accordingly, increase in the radiation level of the nuclear reactor structural materials can be inhibited. (K.M.)

Corrosion in systems for storage and transportation of petroleum products and biofuels identification, monitoring and solutions

CERN Document Server

Groysman, Alec

2014-01-01

This book treats corrosion as it occurs and affects processes in real-world situations, and thus points the way to practical solutions. Topics described include the conditions in which petroleum products are corrosive to metals; corrosion mechanisms of petroleum products; which parts of storage tanks containing crude oils and petroleum products undergo corrosion; dependence of corrosion in tanks on type of petroleum products; aggressiveness of petroleum products to polymeric material; how microorganisms take part in corrosion of tanks and pipes containing petroleum products; which corrosion monitoring methods are used in systems for storage and transportation of petroleum products; what corrosion control measures should be chosen; how to choose coatings for inner and outer surfaces of tanks containing petroleum products; and how different additives (oxygenates, aromatic solvents) to petroleum products and biofuels influence metallic and polymeric materials. The book is of interest to corrosion engineers, mat...

Standard guide for estimating the atmospheric corrosion resistance of low-alloy steels

CERN Document Server

American Society for Testing and Materials. Philadelphia

2004-01-01

1.1 This guide presents two methods for estimating the atmospheric corrosion resistance of low-alloy weathering steels, such as those described in Specifications A242/A242M, A588/A588M, A606 Type 4, A709/A709M grades 50W, HPS 70W, and 100W, A852/A852M, and A871/A871M. One method gives an estimate of the long-term thickness loss of a steel at a specific site based on results of short-term tests. The other gives an estimate of relative corrosion resistance based on chemical composition. 1.2 The values stated in SI units are to be regarded as standard. No other units of measurement are included in this standard.

The study of the corrosion protection of the low-carbon steel using film-products

International Nuclear Information System (INIS)

Aiancului, L.; Millet, Jean-Pierre

2001-01-01

The paper reports studies on the efficiency of the film-inhibitors that covered low-carbon steel placed in a humid medium, and also, the optimization of the working conditions to improve the resistance to corrosion. The analyzes were done in the Industrial Physical - Chemical Laboratories of INSA - Lyon by electrochemical stationary techniques. The experimental device was a potentiometer of type EGG PAR (Princeton Applied Research). It was connected with a computer and three potential electrodes introduced in a cell with NaCl 30 g/l solution to acquire the data and to process the information. The film-products used were organic hydrosoluble polymers with diphosphonic 'heads' that permit a very good absorption at the metallic surface. This research is used to protect the installations of low-carbon steel against the atmospheric and high temperature corrosion. (authors)

An X-ray diffraction study of corrosion products from low carbon steel

International Nuclear Information System (INIS)

Morales, A. L.

2003-01-01

It was found in earlier work a decrease in the corrosion rate from low carbon steel when it was subjected to the action of a combined pollutant concentration (SO 4 ''2-=10''-4 M+Cl=1.5x 10''-3 M). It was also found that large magnetic content of the rust was related to higher corrosion rates. In the present study corrosion products are further analyzed by means of X-ray diffraction to account for composition changes during the corrosion process. it is found that lepidocrocite and goethite are the dominant components for the short-term corrosion in all batches considered while for log-term corrosion lepidocrite and goethite dominates if the corrosion rates is low and magnetite dominates if the corrosion rate is high. The mechanism for decreasing the corrosion rate is related to the inhibition of magnetite production at this particular concentration. (Author) 15 refs

Effect of Aluminum and Silicon on Atmospheric Corrosion of Low-alloying Steel under Containing NaHSO3 Wet/dry Environment

International Nuclear Information System (INIS)

Xinhua, Chen; Junhua, Dong; Enhou, Han; Wei, Ke

2008-01-01

The atmospheric corrosion performance of Al-alloying Si-alloying and Al-Si-alloying steel were studied by wet/dry cyclic corrosion tests (CCT) at 30 .deg. C and 60% relative humidity (RH). The corrosion electrolyte used for CCT was 0.052 wt% NaHSO 3 (pH∼4) solution. The result of gravimetry demonstrated that Al-Si-bearing steels showed lower corrosion resistance than other rusted steels. But the rusted 0.7%Si-alloying steel showed a better corrosion resistance than rusted mild steel. Polarization curves demonstrated that Al-/Si-alloying and Al-Si-alloying improved the rest potential of steel at the initial stage: and accelerated the cathodic reduction and anodic dissolution after a rust layer formed on the surfaces of steels. XRD results showed that Al-Si-alloying decreased the volume fraction of Fe 3 O 4 and α-FeOOH. The recycle of acid accelerated the corrosion of steel at the initial stage. After the rust layer formed on the steel, the leak of rust destabilized the rust layer due to the dissolution of compound containing Al (such as FeAl 2 O 4 , (Fe, Si) 2 (Fe, Al)O 4 ). Al-Si-alloying is hence not suitable for improving the anti-corrosion resistance of steel in industrial atmosphere

Chemical and mechanical control of corrosion product transport

Energy Technology Data Exchange (ETDEWEB)

Hede Larsen, O; Blum, R [I/S Fynsvaerket, Faelleskemikerne, Odense (Denmark); Daucik, K [I/S Skaerbaekvaerket, Faelleskemikerne, Fredericia (Denmark)

1996-12-01

The corrosion products formed in the condensate and feedwater system of once-through boilers are precipitated and deposited inside the evaporator tubes mainly in the burner zone at the highest heat flux. Depositions lead to increased oxidation rate and increased metal temperature of the evaporator tubes, hereby decreasing tube lifetime. This effect is more important in the new high efficiency USC boilers due to increased feedwater temperature and hence higher thermal load on the evaporator tubes. The only way to reduce the load on the evaporator tubes is to minimise corrosion product transport to the boiler. Two general methods for minimising corrosion product transport to the boiler have been evaluated through measurement campaigns for Fe in the water/steam cycle in supercritical boilers within the ELSAM area. One method is to reduce corrosion in the low temperature condensate system by changing conditioning mode from alkaline volatile treatment (AVT) to oxygenated treatment (OT). The other method is to filtrate part of the condensate with a mechanical filter at the deaerator. The results show, that both methods are effective at minimising Fe-transport to the boiler, but changing to OT has the highest effect and should always be used, whenever high purity condensate is maintained. Whether mechanical filtration also is required, depends on the boiler, specifically the load on the evaporator. A simplified calculation model for lifetime evaluation of evaporator tubes has been developed. This model has been used for evaluating the effect of corrosion product transport to the boiler on evaporator tube lifetime. Conventional supercritical boilers generally can achieve sufficient lifetime by AVT and even better by OT, whereas all measures to reduce Fe-content of feedwater, including OT and mechanical filtration, should be taken, to ensure sufficient lifetime for the new boilers with advanced steam data - 290 bar/580 deg. C and above. (au)

Standard practice for conducting atmospheric corrosion tests on metals

CERN Document Server

American Society for Testing and Materials. Philadelphia

2010-01-01

1.1 This practice covers and defines conditions for exposure of metals and alloys to the weather. It sets forth the general procedures that should be followed in any atmospheric test. It is presented as an aid in conducting atmospheric corrosion tests so that some of the pitfalls of such testing may be avoided. As such, it is concerned mainly with panel exposures to obtain data for comparison purposes. 1.2 The values stated in inch-pound units are to be regarded as standard. The values given in parentheses are mathematical conversions to SI units that are provided for information only and are not considered standard. 1.3 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of whoever uses this standard to consult and establish appropriate safety and health practices and determine the applicability of regulatory limitations prior to use.

Surface area and chemical reactivity characteristics of uranium metal corrosion products

International Nuclear Information System (INIS)

Totemeier, T. C.

1998-01-01

The results of an initial characterization of hydride-containing corrosion products from uranium metal Zero Power Physics Reactor (ZPPR) fuel plates are presented. Sorption analyses using the BET method with a Kr adsorbate were performed to measure the specific areas of corrosion product samples. The specific surface areas of the corrosion products varied from 0.66 to 1.01 m 2 /g. The reactivity of the products in Ar-9%O 2 and Ar-20%O 2 were measured at temperatures between 35 C and 150 C using a thermo-gravimetric analyzer. Ignition of the products occurred at temperatures of 150 C and above. The oxidation rates below ignition were comparable to rates observed for uranium metal

Electrochemical noise evaluation of anodized aluminum. Comparative study against corrosion behaviour in the atmosphere

International Nuclear Information System (INIS)

Betancourt, N.; Corvo, F.; Mendoza, A.; Simancas, J.; Morcillo, M.; Gonzalez, J. A.; Fragata, F.; Pena, J. J.; Sanchez de Villalaz, M.; Flores, S.; Almeida, E.; Rivero, S.; Rincon, O. T. de.

2003-01-01

The present work reports the evaluation of aluminum and anodized aluminum by electrochemical noise, as a part of the PATINE/CYTED project of the working group NS5. A visual examination is also made. The samples were exposed at several Ibero-American atmospheres up to 2 years of exposure. Different thickness of anodized aluminum were evaluated. The electrochemical potential noise of the 5 μm unexposed sample (pattern) showed a different behaviour to that showed by the other anodized specimens. This could be due to a slower sealed of the samples of higher thickness. The same behavior was observed on the samples exposed at the rural station. el Pardo. According to the visual examination, the samples of bare aluminum and those of anodized 5 μm thickness were the most affected by pitting corrosion in the highly polluted atmospheres. A good correlation between corrosion behaviour determined by visual examination and EN was obtained. (Author) 4 refs

Recent Research and Development in Solving Atmospheric Corrosion Problems of Steel Industries in Japan

International Nuclear Information System (INIS)

Yamashita, M.; Uchida, H.

2002-01-01

A rust layer, so called 'protective' rust layer, on a weathering low-alloy steel has strong protective ability for atmospheric corrosion of the steel. We have recently found through a large number of spectroscopic studies including Moessbauer spectroscopy that the protective rust layer forms after long-term phase transformation. The phase and structure of the rust definitely control the protective ability of the rust layer. From this recent knowledge, some new technologies have been developed. One is the surface-treatment technique that provides a possibility for obtaining the protective rust layer in a relatively short period even in the severe environments such as in marine and chloride (de-icing salts) containing environments. Others are based on selection of effective alloying elements for steel materials. These are particularly important for application in areas where protective rust layer formation may be hindered or prevented. In this paper, we mention recent progress in research and development on rusting protection by rust for atmospheric corrosion of steels in Japan.

Bioaccumulation and food chain transfer of corrosion products from radioactive stainless steel

International Nuclear Information System (INIS)

Young, J.S.

1986-07-01

Two sets of experiments were conducted to determine if corrosion products from radioactive Type 347 stainless steel could be biologically transferred from sediment through a marine food chain, and whether corrosion products dissolved in seawater could be bioaccumulated and then eliminated. Corrosion products containing 60 Co and 63 Ni from the radioactive stainless steel were introduced into marine sediments. Infaunal polychaete worms exposed to these sediments bioaccumulated the radionuclides. The feeding of these worms to shrimp and fish resulted in a trophic transfer of the radioactive products across a one-step food chain. The magnitude of the transfers are described in terms of transfer factors. Dissolved corrosion products as measured by the radionuclides were also bioaccumulated by shrimp and fish concentrating more than fish. Concentration factors were calculated

Surface area and chemical reactivity characteristics of uranium metal corrosion products.

Energy Technology Data Exchange (ETDEWEB)

Totemeier, T. C.

1998-02-17

The results of an initial characterization of hydride-containing corrosion products from uranium metal Zero Power Physics Reactor (ZPPR) fuel plates are presented. Sorption analyses using the BET method with a Kr adsorbate were performed to measure the specific areas of corrosion product samples. The specific surface areas of the corrosion products varied from 0.66 to 1.01 m{sup 2}/g. The reactivity of the products in Ar-9%O{sub 2} and Ar-20%O{sub 2} were measured at temperatures between 35 C and 150 C using a thermo-gravimetric analyzer. Ignition of the products occurred at temperatures of 150 C and above. The oxidation rates below ignition were comparable to rates observed for uranium metal.

Corrosion resistance of zinc-magnesium coated steel

International Nuclear Information System (INIS)

Hosking, N.C.; Stroem, M.A.; Shipway, P.H.; Rudd, C.D.

2007-01-01

A significant body of work exists in the literature concerning the corrosion behaviour of zinc-magnesium coated steel (ZMG), describing its enhanced corrosion resistance when compared to conventional zinc-coated steel. This paper begins with a review of the literature and identifies key themes in the reported mechanisms for the attractive properties of this material. This is followed by an experimental programme where ZMG was subjected to an automotive laboratory corrosion test using acidified NaCl solution. A 3-fold increase in time to red rust compared to conventional zinc coatings was measured. X-ray diffraction, X-ray photoelectron spectroscopy and scanning electron microscopy were used to characterize the corrosion products formed. The corrosion products detected on ZMG included simonkolleite (Zn 5 Cl 2 (OH) 8 . H 2 O), possibly modified by magnesium uptake, magnesium hydroxide (Mg(OH) 2 ) and a hydroxy carbonate species. It is proposed that the oxygen reduction activity at the (zinc) cathodes is reduced by precipitation of alkali-resistant Mg(OH) 2 , which is gradually converted to more soluble hydroxy carbonates by uptake of atmospheric carbon dioxide. This lowers the surface pH sufficiently to allow thermodynamically for general precipitation of insoluble simonkolleite over the corroding surface thereby retarding the overall corrosion reactions, leaving only small traces of magnesium corrosion products behind. Such a mechanism is consistent with the experimental findings reported in the literature

Analysis of corrosion product transport in PWR primary system under non-convective condition

International Nuclear Information System (INIS)

Han, Byoung Sub

1992-02-01

The increase of occupational radiation exposure (ORE) due to the increase of the operational period at existing nuclear power plant and also the publication of the new version of ICRP recommendation (ICRP publication No. 60) for radiological protection require much more strict reduction of radiation buildup in the nuclear power plant. The major sources of the radiation, i.e. the radioactive corrosion-products, are generated by the neutron activation of the corrosion products at the reactor core, and then the radioactive corrosion products are transported to the outside of the core, and accumulated near the steam generator side at PWR. Major radioactive corrosion-products of interest in PWR are Cr 51 ,: Mn 54 ,: Co 58 ,: Fe 59 and Co 60 . Among them Co 58 and Co 60 are known to contribute approximately more than 70% of the total ORE. Thus our main concerns are focused on predicting the transport and deposition of the Co radionuclides and suggesting the optimizing method which can minimize and control the ORE of the nuclear power plant. It is well known that Co-source is most effectively controlled by pH-solubility radiation control, and also some complex computer codes such as CORA and PACTOLE have been developed and revised to predict the corrosion product behavior. However these codes still imply some intrisic problems in simulating the real behavior of corrosion products in the reactor because of 1) the lack of important experimental data, coefficients and parameters of the transport and reactions under actual high temperature and pressure conditions, 2) no general theoretical modelling which can describe such many different mechanisms involved in the corrosion product movements, 3) the newly developed and measured behavior of the corrosion product transport mechanism. Since no sufficient and detailed information is available from the above-mentioned codes (also due to propriority problems), we concentrate on developing a new computer code, CP-TRAN (Corrosion

Characterization of uranium corrosion products involved in the March 13, 1998 fuel manufacturing facility pyrophoric event

International Nuclear Information System (INIS)

Totemeier, T.C.

1999-01-01

Uranium metal corrosion products from ZPPR fuel plates involved in the March 13, 1998 pyrophoric event in the Fuel Manufacturing Facility at Argonne National Laboratory-West were characterized using thermo-gravimetric analysis, X-ray diffraction, and BET gas sorption techniques. Characterization was performed on corrosion products in several different conditions: immediately after separation from the source metal, after low-temperature passivation, after passivation and extended vault storage, and after burning in the pyrophoric event. The ignition temperatures and hydride fractions of the corrosion product were strongly dependent on corrosion extent. Corrosion products from plates with corrosion extents less than 0.7% did not ignite in TGA testing, while products from plates with corrosion extents greater than 1.2% consistently ignited. Corrosion extent is defined as mass of corrosion products divided by the total mass of uranium. The hydride fraction increased with corrosion extent. There was little change in corrosion product properties after low-temperature passivation or vault storage. The burned products were not reactive and contained no hydride; the principal constituents were UO 2 and U 3 O 7 . The source of the event was a considerable quantity of reactive hydride present in the corrosion products. No specific ignition mechanism could be conclusively identified. The most likely initiator was a static discharge in the corrosion product from the 14th can as it was poured into the consolidation can. The available evidence does not support scenarios in which the powder in the consolidation can slowly self-heated to the ignition point, or in which the powder in the 14th can was improperly passivated

Characterization of uranium corrosion products involved in the March 13, 1998 fuel manufacturing facility pyrophoric event.

Energy Technology Data Exchange (ETDEWEB)

Totemeier, T.C.

1999-04-26

Uranium metal corrosion products from ZPPR fuel plates involved in the March 13, 1998 pyrophoric event in the Fuel Manufacturing Facility at Argonne National Laboratory-West were characterized using thermo-gravimetric analysis, X-ray diffraction, and BET gas sorption techniques. Characterization was performed on corrosion products in several different conditions: immediately after separation from the source metal, after low-temperature passivation, after passivation and extended vault storage, and after burning in the pyrophoric event. The ignition temperatures and hydride fractions of the corrosion product were strongly dependent on corrosion extent. Corrosion products from plates with corrosion extents less than 0.7% did not ignite in TGA testing, while products from plates with corrosion extents greater than 1.2% consistently ignited. Corrosion extent is defined as mass of corrosion products divided by the total mass of uranium. The hydride fraction increased with corrosion extent. There was little change in corrosion product properties after low-temperature passivation or vault storage. The burned products were not reactive and contained no hydride; the principal constituents were UO{sub 2} and U{sub 3}O{sub 7}. The source of the event was a considerable quantity of reactive hydride present in the corrosion products. No specific ignition mechanism could be conclusively identified. The most likely initiator was a static discharge in the corrosion product from the 14th can as it was poured into the consolidation can. The available evidence does not support scenarios in which the powder in the consolidation can slowly self-heated to the ignition point, or in which the powder in the 14th can was improperly passivated.

Application of electromagnetic fields to improve the removal rate of radioactive corrosion products

International Nuclear Information System (INIS)

Kong, Tae Young; Lee, Kun Jai; Song, Min Chul

2004-01-01

To comply with increasingly strict regulations for protection against radiation exposure, many nuclear power plants have been working ceaselessly to reduce and control both the radiation sources within power plants and the radiation exposure experienced by operational and maintenance personnel. Many research studies have shown that deposits of irradiated corrosion products on the surfaces of coolant systems are the main cause of occupational radiation exposure in nuclear power plants. These corrosion product deposits on the fuel-clad surface are also known to be main factors in the onset of Axial Offset Anomaly (AOA). Hence, there is a great deal of ongoing research on water chemistry and corrosion processes. In this study, a magnetic filter with permanent magnets was devised to remove the corrosion products in the coolant stream by taking advantage of the magnetic properties of the corrosion particles. Experiments using permanent magnets to filter the corrosion products demonstrated a removal efficiency of over 90% for particles above 5 μm. This finding led to the construction of an electromagnetic device that causes the metallic particulates to flocculate into larger aggregates of about 5 μm in diameter by using a novel application of electromagnetic flocculation on radioactive corrosion products

Capturing device for radioactive corrosion products

International Nuclear Information System (INIS)

Ono, Kiyoshi.

1987-01-01

Purpose: To render the flow channel area uniform for each of coolants over the entire capturing device and reduce the corrosion of capturing materials due to coolants. Constitution: Most of radioactivity caused by radioactive corrosion products are due to Mn-54 radioactive nuclides and it has been known that the nuclides are readily deposited to the surface of nickel material in sodium at high temperature. It is difficult in a conventional capturing device constituted by winding a nickel plate fabricated with protrusions in a multiple-coaxial configuration, that the flow channel area is reduced in a portion of the flow channel and it is difficult to make the flow of the coolants uniform. In view of the above, by winding a nickel plate having a plurality of protrusions at the surface formed integrally by way of an electrolytic process into a multiple-coaxial or spiral shape, those having high resistance to the coolant corrosion can be obtained. (Takahashi, M.)

Application of Moessbauer spectroscopy on corrosion products of NPP

Energy Technology Data Exchange (ETDEWEB)

Dekan, J., E-mail: julius.dekan@stuba.sk; Lipka, J.; Slugen, V. [Institute of Nuclear and Physical Engineering, Faculty of Electrical Engineering and Information Technology, SUT (Slovakia)

2013-04-15

Steam generator (SG) is generally one of the most important components at all nuclear power plants (NPP) with close impact to safe and long-term operation. Material degradation and corrosion/erosion processes are serious risks for long-term reliable operation. Steam generators of four VVER-440 units at nuclear power plants V-1 and V-2 in Jaslovske Bohunice (Slovakia) were gradually changed by new original 'Bohunice' design in period 1994-1998, in order to improve corrosion resistance of SGs. Corrosion processes before and after these design and material changes in Bohunice secondary circuit were studied using Moessbauer spectroscopy during last 25 years. Innovations in the feed water pipeline design as well as material composition improvements were evaluated positively. Moessbauer spectroscopy studies of phase composition of corrosion products were performed on real specimens scrapped from water pipelines or in form of filters deposits. Newest results in our long-term corrosion study confirm good operational experiences and suitable chemical regimes (reduction environment) which results mostly in creation of magnetite (on the level 70 % or higher) and small portions of hematite, goethite or hydrooxides. Regular observation of corrosion/erosion processes is essential for keeping NPP operation on high safety level. The output from performed material analyses influences the optimisation of operating chemical regimes and it can be used in optimisation of regimes at decontamination and passivation of pipelines or secondary circuit components. It can be concluded that a longer passivation time leads more to magnetite fraction in the corrosion products composition.

Properties of Douglas Point Generating Station heat transport corrosion products

International Nuclear Information System (INIS)

Montford, B.; Rummery, T.E.

1975-09-01

Chemical, radiochemical and structural properties of circulating and fixed corrosion products from the Douglas Point Generating Station are documented. Interaction of Monel-400 and carbon steel corrosion products is described, and the mechanisms of Monel-400 surface deposit release, and activity buildup in the coolant system, are briefly discussed. Efficiencies of filters and ion-exchangers for the removal of released radionuclides are given. (author)

Effect of corrosive marine atmosphere on construction materials in Tanzania: Exposure sites and preliminary results

International Nuclear Information System (INIS)

Mmari, A.G.; Uiso, C.B.S.; Makundi, I.N.; Potgieter-Vermaak, S.S.; Potgieter, J.H.; Van Grieken, R.

2007-01-01

Air pollution studies in Africa are limited and the influence of ambient air quality on buildings and constructions have not been investigated in the larger part of Sub-Saharan Africa. The increasing burden of emission from industry, traffic and coal power plants on ambient air pollution in Sub-Saharan Africa necessitated reviewing previous and current studies. In South Africa a 20-year exposure program, focusing on the effect of ambient exposure on various metals and alloys, showed that the amount of rainfall, relative humidity, atmospheric pollution, wind speed, solar radiation and structural design are some of the factors controlling atmospheric corrosion. Tanzania, being among the Sub-Saharan African countries and partly bordered by Indian ocean, the main source of marine atmosphere, experiences corrosive degradation on metal roofing and cementitious materials. This paper describes the exposure site set-up and will report on some preliminary results of air quality and its relation with the meteorological conditions, as well as surface changes observed, for the year one of exposure. These will thereafter be compared to the completed European and Asian studies, as reported by CLRTAP and RAPIDC respectively. (author)

Evolution of corrosion of MnCuP weathering steel submitted to wet/dry cyclic tests in a simulated coastal atmosphere

International Nuclear Information System (INIS)

Hao Long; Zhang Sixun; Dong Junhua; Ke Wei

2012-01-01

Highlights: ► The evolution of rust on MnCuP weathering steel submitted to a simulated coastal atmosphere has been investigated. ► The corrosion evolution of MnCuP weathering steel can be divided into two stages with distinct rust properties. ► A protective rust layer with higher amounts of α-FeOOH and lower Fe 3 O 4 forms as the corrosion proceeds. ► The rust initially enhances and then stabilizes the cathodic process, but the anodic process tends to be inhibited. - Abstract: The evolution of rust on MnCuP weathering steel submitted to a simulated coastal atmosphere was investigated by corrosion weight gain, scanning electron microscopy, X-ray diffraction, and electrochemical methods. The results indicate that the higher corrosion rate during the first stage than that during the second stage is related closely to the rust composition and electrochemical properties. The corrosion rate evolution is caused by the formation of a protective rust layer with a higher relative amount of α-FeOOH. The rust initially enhances and then stabilizes the cathodic process, but the anodic process tends to be inhibited by the protective rust layer.

Technical investigation of a pyrophoric event involving corrosion products from HEU ZPPR fuel plates

International Nuclear Information System (INIS)

Totemeier, T. C.

2000-01-01

A pyrophoric event recently occurred which involved corrosion products collected from highly-enriched uranium (HEU) fuel plates used in the Zero Power Physics Reactor (ZPPR). This paper summarizes the event and its background, and presents the results of an investigation into its source and mechanism. The investigation focused on characterization of corrosion product samples similar to those involved in the event using thermo-gravimetric analysis (TGA). Burning curve TGA tests were performed to measure the ignition temperature and hydride fractions of corrosion products in several different conditions to assess the effects of passivation treatment and long-term storage on chemical reactivity. The hydride fraction and ignition temperature of the corrosion products were found to be strongly dependent on the corrosion extent of the source metal. The results indicate that the energy source for the event was a considerable quantity of uranium hydride present in the corrosion products, but the specific ignition mechanism could not be identified

Accelerated Test Method for Corrosion Protective Coatings Project

Science.gov (United States)

Falker, John; Zeitlin, Nancy; Calle, Luz

2015-01-01

This project seeks to develop a new accelerated corrosion test method that predicts the long-term corrosion protection performance of spaceport structure coatings as accurately and reliably as current long-term atmospheric exposure tests. This new accelerated test method will shorten the time needed to evaluate the corrosion protection performance of coatings for NASA's critical ground support structures. Lifetime prediction for spaceport structure coatings has a 5-year qualification cycle using atmospheric exposure. Current accelerated corrosion tests often provide false positives and negatives for coating performance, do not correlate to atmospheric corrosion exposure results, and do not correlate with atmospheric exposure timescales for lifetime prediction.

Corrosion mechanisms of containment glasses for fission products

International Nuclear Information System (INIS)

Nogues, J.L.

1984-01-01

After a review of nuclear energy production and waste vitrification principles, the aqueous corrosion mechanisms of the containment glasses and the various parameters affecting the corrosion are studied: effects of glass composition, temperature, lixiviation agent pH, lixiviation duration and mode. Conventional mass loss measurement and solution analyses are coupled to sophisticated surface analysis techniques. The hydrolyzed layer formation and the solubility limits are discussed. 87 figs., 30 tabs., 144 refs

Some in-reactor loop experiments on corrosion product transport and water chemistry

International Nuclear Information System (INIS)

Balakrishnan, P.V.; Allison, G.M.

1978-01-01

A study of the transport of activated corrosion products in the heat transport circuit of pressurized water-cooled nuclear reactors using an in-reactor loop showed that the concentration of particulate and dissolved corrosion products in the high-temperature water depends on such chemical parameters as pH and dissolved hydrogen concentration. Transients in these parameters, as well as in temperature, generally increase the concentration of suspended corrosion products. The maximum concentration of particles observed is much reduced when high-flow, high-temperature filtration is used. Filtration also reduces the steady-state concentration of particles. Dissolved corrosion products are mainly responsible for activity accumulation on surfaces. The data obtained from this study were used to estimate the rate constants for some of the transfer processes involved in the contamination of the primary heat transport circuit in water-cooled nuclear power reactors

Mitigation of corrosion product ingress into SG's

International Nuclear Information System (INIS)

Han, S.H.

1988-01-01

Design and operation experiences to mitigate corrosion product ingress into SGs in Korea nuclear power plants are briefly reviewed. Maintaining the feedwater pH above 9.6 with morpholine seems to contribute significantly to reduction of iron transport to SGs. Measured iron transport rates were 4.8 g/hr/100 MWe at pH 9.8 and 2.8 g/hr/100 MWe at 9.3, respectively. Removal of corrosion products through SG blowdown is very limited. Its removal efficiency at the higher pH plant was in the neighborhood of 10 %. In one of the Korea Nuclear Units, a large amount of sludge piles were found in the middle of tube bundles especially on the cold leg side. Damaged tubes were identified by the multi-frequency eddy current tests and plugged later during the refueling period. Intermittent blowdown-rate increase was tried to enhance ionic impurity removal through SG blowdown. Even though it was not effective against Na, removal other impurity was improved, resulting in prolonged condensate polisher operation periods by 1 - 2 days. Two-bed polisher design, a cation bed followed by a mixed bed, was chosen for future PWR plants to enhance corrosion product filtering capability of the polishers. Condensate pump discharge polishing and divided hot well polishing methods are currently in consideration. (Nogami, K.)

Copper corrosion experiments under anoxic conditions

Energy Technology Data Exchange (ETDEWEB)

Ollila, Kaija [VTT Technical Research Centre of Finland, Espoo (Finland)

2013-06-15

This report gives results from the corrosion experiments with copper under anoxic conditions. The objective was to study whether hydrogen-evolving corrosion reaction could occur. Copper foil samples were exposed in deaerated deionized water in Erlenmeyer flasks in the glove box with inert atmosphere. Four corrosion experiments (Cu1, Cu2, Cu3 and Cu4) were started, as well as a reference test standing in air. Cu1 and Cu2 had gas tight seals, whereas Cu3 and Cu4 had palladium foils as hydrogen permeable enclosure. The test vessels were stored during the experiments in a closed stainless steel vessel to protect them from the trace oxygen of the gas atmosphere and light. After the reaction time of three and a half years, there were no visible changes in the copper surfaces in any of the tests in the glove box, in contrast the Cu surfaces looked shiny and unaltered. The Cu3 test was terminated after the reaction time of 746 days. The analysis of the Pd-membrane showed the presence of H2 in the test system. If the measured amount of 7.2{center_dot}10{sup 5} mol H{sub 2} was the result of formation of Cu{sub 2}O this would correspond to a 200 nm thick corrosion layer. This was not in agreement with the measured layer thickness with SIMS, which was 6{+-}1 nm. A clear weight loss observed for the Cu3 test vessel throughout the test period suggests the evaporation of water through the epoxy sealing to the closed steel vessel. If this occurred, the anaerobic corrosion of steel surface in humid oxygen-free atmosphere could be a source of hydrogen. A similar weight loss was not observed for the parallel test (Cu4). The reference test standing in air showed visible development of corrosion products.

Influence of climatic factors and pollution on the atmospheric corrosion of steels. Laboratory measurements

International Nuclear Information System (INIS)

Muylder, Jean van; Pourbaix, Marcel

1977-01-01

The influence of climatic and polluting factors on the atmospheric corrosion of four steels has been examined in the laboratory by an original accelerated electrochemical testing method. This research has led notably to the following conclusions: the corrosion behavior of the steels very much depends on the chloride- and SO 2 -contents of the rain water, as well as on the temperature of the metal during the drying periods. The best patinas have been obtained by submitting the steel successively to the corroding action of a solution of bisulphite and to the alternate actions of non-polluted rains and of drying, preferably at about 60 0 C. As a result of this, the formation of a protective patina may be accelerated by different methods. The relative merits of different steels under different conditions of atmospheric exposure may be predetermined by laboratory tests lasting several weeks. It is useful, when exposing steels in natural exposure sites, to measure as often as feasible the electrode potentials and the temperature of the steel specimens

Rhenium Uptake as Analogue 96Tc by Steel Corrosion Products

International Nuclear Information System (INIS)

K.M. Krupka; C.F. Brown; H. Todd Schaef; S. M. Heald; M. M. Valenta; B. W. Arey

2006-01-01

Static batch experiments were used to examine the sorption of dissolved perrhenate [Re(VII)], as a surrogate for pertechnetate [Tc(VII)], on corrosion products of A-516 carbon steel coupons contacted with synthetic groundwater or dilute water. After 109 days of contact time, the concentration of dissolved Re(VII) in the synthetic groundwater matrix decreased by approximately 26%; the dilute water matrix experienced a 99% decrease in dissolved Re(VII) over the same time period. Bulk x-ray diffraction (XRD) results for the corroded steel coupons showed that the corrosion products consisted primarily of maghemite, lepidocrocite, and goethite. Analyses of the coupons by scanning electron microscopy/energy dispersive spectroscopy (SEM/EDS) indicated that Re was present with the morphologically complex assemblages of Fe oxide/hydroxide corrosion products for samples spiked with the highest dissolved Re(VII) concentration (1.0 mmol/L) used for these experiments. Analyses of corroded steel coupons contacted with solutions containing 1.0 mmol/L Re(VII) by synchrotron-based methods confirmed the presence of Re sorbed with the corrosion product on the steel coupons. Analyses showed that the Re sorbed on these corroded coupons was in the +7 oxidation state, suggesting that the Re(VII) uptake mechanism did not involve reduction of Re to a lower oxidation state, such as +4. The results of our studies using Re(VII) as an analogue for 99 Tc(VII) suggest that 99 Tc(VII) would also be sorbed with steel corrosion products and that the inventory of 99 Tc(VII) released from breached waste packages would be lower than what is now conservatively estimated

Corrosion-electrochemical behavior of nickel in an alkali metal carbonate melt under a chlorine-containing atmosphere

Science.gov (United States)

Nikitina, E. V.; Kudyakov, V. Ya.; Malkov, V. B.; Plaksin, S. V.

2013-08-01

The corrosion-electrochemical behavior of a nickel electrode is studied in the melt of lithium, sodium, and potassium (40: 30: 30 mol %) carbonates in the temperature range 500-600°C under an oxidizing atmosphere CO2 + 0.5O2 (2: 1), which is partly replaced by gaseous chlorine (30, 50, 70%) in some experiments. In other experiments, up to 5 wt % chloride of sodium peroxide is introduced in a salt melt. A change in the gas-phase composition is shown to affect the mechanism of nickel corrosion.

Characterization of the corrosion products formed on mild steel in acidic medium with N-octadecylpyridinium bromide as corrosion inhibitor

Energy Technology Data Exchange (ETDEWEB)

Nava, N., E-mail: tnava@imp.mx; Likhanova, N. V. [Direccion de Investigacion y Posgrado, Instituto Mexicano del Petroleo (Mexico); Olivares-Xometl, O. [Benemerita Universidad Autonoma de Puebla, Facultad de Ingenieria Quimica (Mexico); Flores, E. A. [Direccion de Investigacion y Posgrado, Instituto Mexicano del Petroleo (Mexico); Lijanova, I. V. [CIITEC, Instituto Politecnico Nacional (Mexico)

2011-11-15

The characterization of the corrosion products formed on mild steel SAE 1018 after 2 months exposure in aqueous sulfuric acid with and without corrosion inhibitor N-octadecylpyridinium bromide has been carried out by means of transmission {sup 57}Fe Moessbauer spectroscopy and X-ray powder diffraction (XRD). The major constituent of the rust formed in this environment without corrosion inhibitor is goethite ({alpha}-FeOOH). The samples with N-octadecylpyridinium bromide contain rozenite and large amounts of melanterite in the corrosion layers.

Synthesis and Structures of Pb3O2(CH3COO)2 · 0.5H2O and Pb2O(HCOO)2: Two Corrosion Products Revisited

International Nuclear Information System (INIS)

Mauck, Catherine M.; van den Heuvel, Titus W.P.; Hull, Michaela M.; Zeller, Matthias; Oertel, Catherine M.

2010-01-01

Reactions of carboxylic acids with lead play an important role in the atmospheric corrosion of lead and lead-tin alloys. This is of particular concern for the preservation of lead-based cultural objects, including historic lead-tin alloy organ pipes. Two initial corrosion products, Pb 3 O 2 (CH 3 COO) 2 · 0.5H 2 O (1) and Pb 2 O(HCOO) 2 (2), had been identified through powder diffraction fingerprints in the Powder Diffraction File, but their structures had never been determined. We have crystallized both compounds using hydrothermal solution conditions, and structures were determined using laboratory and synchrotron single-crystal X-ray diffraction data. Compound 1 crystallizes in P t , and 2 in Cccm. These compounds may be viewed as inorganic-organic networks containing single and double chains of edge-sharing Pb 4 O tetrahedra and have structural similarities to inorganic basic lead compounds. Bond valence sum analysis has been applied to the hemidirected lead coordination environments in each compound. Atmospheric exposure experiments contribute to understanding of the potential for conversion of these short-term corrosion products to hydrocerussite, Pb 3 (CO 3 ) 2 (OH) 2 , previously identified as a long-term corrosion product on lead-rich objects. Each compound was also characterized by elemental analysis, thermogravimetric analysis and differential scanning calorimetry (TGA-DSC), and Raman spectroscopy.

Corrosion '98: 53. annual conference and exposition, proceedings

International Nuclear Information System (INIS)

Anon.

1998-01-01

This conference was divided into the following sections: Corrosion in Gas Treating; Problems and Solutions in Commercial Building Water Systems; Green Corrosion/Scale Inhibitors; Atmospheric Corrosion; AIRPOL Update/98; Rubber Lining--Answers to Many Problems; Interference Problems; Environmental Assisted Cracking: Fundamental Research and Industrial Applications; Corrosion in Nuclear Systems; New Developments in Scale and Deposit Control; Corrosion and Corrosion Protection in the Transportation Industries; What's All the Noise About--Electrochemical That Is; Refining Industry Corrosion; Corrosion Problems in Military Hardware: Case Histories, Fixes and Lessons Learned; Cathodic Protection Test Methods and Instrumentation for Underground and On-grade Pipelines and Tanks; Recent Developments in Volatile Corrosion Inhibitors; Corrosion in Supercritical Fluids; Microbiologically Influenced Corrosion; Advances in Understanding and Controlling CO 2 Corrosion; Managing Corrosion with Plastics; Material Developments for Use in Exploration and Production Environments; Corrosion in Cold Regions; The Effect of Downsizing and Outsourcing on Cooling System Monitoring and Control Practices; New Developments in Mechanical and Chemical Industrial Cleaning; Mineral Scale Deposit Control in Oilfield Related Operations; Biocides in Cooling Water; Corrosion and Corrosion Control of Reinforced Concrete Structures; Materials Performance for Fossil Energy Conversion Systems; Marine corrosion; Thermal Spray--Coating and Corrosion Control; Flow Effects on Corrosion in Oil and Gas Production; Corrosion Measurement Technologies; Internal Pipeline Monitoring--Corrosion Monitoring, Intelligent Pigging and Leak Detection; Cathodic Protection in Natural Waters; Corrosion in Radioactive Liquid Waste Systems; On-line Hydrogen Permeation Monitoring Equipment and Techniques, State of the Art; Water Reuse and Recovery; Performance of Materials in High Temperature Environments; Advances in Motor

Simulations of corrosion product transfer with the OSCAR V1.2 code

International Nuclear Information System (INIS)

Dacquait, F.; Francescatto, J.; Broutin, F.; Genin, J.B.; Benier, G.; Girard, M.; You, D.; Ranchoux, G.; Bonnefon, J.; Bachet, M.; Riot, G.

2012-09-01

Activated Corrosion Products (ACPs) generate a radiation field in PWRs, which is the major contributor to the dose absorbed by nuclear power plant staff working during shutdown operations and maintenance. Therefore, a thorough understanding of the mechanisms that control the corrosion product transfer is of the highest importance. Since the 1970's, the R and D strategy in France has been based on experiments in test loops representative of PWR conditions, on in-situ gamma spectrometry measurements of the PWR primary system contamination and on simulation code development. The simulation of corrosion product transfers in PWR primary circuits is a major challenge since it involves many physical and chemical phenomena including: corrosion, dissolution, precipitation, erosion, deposition, convection, activation... In addition to the intrinsic difficulty of multi-physics modelling, the primary systems present severe operating conditions (300 deg. C, 150 bar, neutron flux, fluid velocity up to 15 m.s -1 and very low corrosion product concentrations). The purpose of the OSCAR code, developed by the CEA in cooperation with EDF and AREVA NP, is to predict the PWR primary system contamination by corrosion and fission products. The OSCAR code is considered to be not only a tool for numerical simulations and predictions (operational practices improvements and new-built PWRs design) but also one that might combine and organise all new knowledge useful to progress on contamination. The OSCAR code for Products of Corrosion, OSCAR PC, allows researchers to analyse the corrosion product behaviour and to calculate the ACP volume and surface activities of the primary and auxiliary systems. In the new version, OSCAR PC V1.2, the corrosion product transfer in the particulate form is enhanced and a new feature is the possibility to simulate cold shutdowns. In order to validate this version, the contamination transfer has been simulated in 5 French PWRs with different operating and

Corrosion of beryllium

International Nuclear Information System (INIS)

Mueller, J.J.; Adolphson, D.R.

1987-01-01

The corrosion behavior of beryllium in aqueous and elevated-temperature oxidizing environments has been extensively studied for early-intended use of beryllium in nuclear reactors and in jet and rocket propulsion systems. Since that time, beryllium has been used as a structural material in les corrosive environments. Its primary applications include gyro systems, mirror and reentry vehicle structures, and aircraft brakes. Only a small amount of information has been published that is directly related to the evaluation of beryllium for service in the less severe or normal atmospheric environments associated with these applications. Despite the lack of published data on the corrosion of beryllium in atmospheric environments, much can be deduced about its corrosion behavior from studies of aqueous corrosion and the experiences of fabricators and users in applying, handling, processing, storing, and shipping beryllium components. The methods of corrosion protection implemented to resist water and high-temperature gaseous environments provide useful information on methods that can be applied to protect beryllium for service in future long-term structural applications

Long term corrosion of iron in concrete and in atmospheric conditions: a contribution of archaeological analogues to mechanism comprehension

International Nuclear Information System (INIS)

Burger, E.; Demoulin, A.; Dillman, Ph.; Neff, D.; Berge, P.; Burger, E.; Perrin, St.; L'hostis, V.; Dillman, Ph.; Millard, A.

2009-01-01

Full text of publication follows: The prediction of iron (or low alloy steel) corrosion on very long term period is necessary in two different purposes: (i) the preservation and conservation of cultural heritage and (ii) the French storage and repository concept for the radioactive wastes. In order to determine the evolution of corrosion processes for very long period, mechanistic models have been developed. In these models that are based on a phenomenological approach to evaluate the average corrosion rates, two different environments are considered: concrete (steel reinforcements) and atmospheric. The study of archaeological analogues is a very pertinent tool for the validation of these models. First, physico-chemical analysis on old corrosion layers lead to a precise localisation and identification of the phases present in the corrosion system. Moreover, experimental reinduced corrosions of ancient samples under controlled parameters (temperature, relative humidity) bring new insight on the mechanisms involved. In particular, one crucial question related to the wet-dry cycle is the localisation of oxygen reduction sites in the rust layer. For this purpose, specific experiments have been set up to re-corrode the ancient samples in marked medium (using 18 O 2 ). Samples were exposed to cycling between high and low relative humidity, produced by saline saturated solutions. Then cross-sections of samples obtained were investigated by nuclear reaction analysis (NRA) 18 O(p,α) 15 N on the Pierre Sue Laboratory nuclear microprobe. In this presentation the 18 O distribution profiles are discussed and interpreted in order to bring new insight on corrosion mechanisms. A comparative interpretation is made for each medium (concrete and atmosphere)

Corrosion behavior of metals and alloys in marine-industrial environment

Directory of Open Access Journals (Sweden)

Mariappan Natesan, Subbiah Selvaraj, Tharmakkannu Manickam and Gopalachari Venkatachari

2008-01-01

Full Text Available This work deals with atmospheric corrosion to assess the degrading effects of air pollutants on ferrous and non-ferrous metals and alloys, which are mostly used as engineering materials. An exposure study was conducted in the Tuticorin port area located on the east coast of South India, in the Gulf of Mannar with Sri Lanka to the southeast. Common engineering materials, namely mild steel, galvanized iron, Zn, Al, Cu and Cu–Zn alloys (Cu–27Zn, Cu–30Zn and Cu–37Zn, were used in the investigation. The site was chosen where the metals are exposed to marine and industrial atmospheres. Seasonal 1 to 12 month corrosion losses of these metals and alloys were determined by a weight loss method. The weight losses showed strong corrosion of mild steel, galvanized iron, Cu and Zn and minor effect on Al and Cu–Zn alloys. Linear regression analysis was conducted to study the mechanism of corrosion. The composition of corrosion products formed on the metal surfaces was identified by x-ray diffraction and Fourier transform infrared spectroscopy.

Corrosion products in the coolant circuits of PWR nuclear power plants

International Nuclear Information System (INIS)

Darras, R.

1984-01-01

The characteristics of corrosion products formed in the primary and secondary circuits of pressurized light water nuclear power plants are first briefly recalled. The problem set by the pollution of coolants and metallic surfaces is then examined. Finally, the measures of precaution to take and the possible solutions to minimize the disturbing effects of this pollution by corrosion products are presented [fr

A contribution to the modelling of atmospheric corrosion of iron

International Nuclear Information System (INIS)

Hoerle, S.; Mazaudier, F.

2003-01-01

With the aim of predicting the long term atmospheric corrosion behaviour of iron, the characteristics of the rust layer formed during this process and the mechanisms occurring inside the rust layer during a wet-dry cycle are considered. A first step in modelling the behaviour is proposed, based on the description of the cathodic reactions associated with iron oxidation: reduction of a part of the rust layer (lepidocrocite) and reduction of dissolved oxygen on the rust layer. The modelling, by including some composition and morphological data of the rust layer as parameters, is able to account for the metal damage after one Wet-Dry cycle. (authors)

Study on Increasing High Temperature pH(t) to Reduce Iron Corrosion Products

International Nuclear Information System (INIS)

Shin, Dong Man; Hur, Nam Yong; Kim, Waang Bae

2011-01-01

The transportation and deposition of iron corrosion products are important elements that affect both the steam generator (SG) integrity and secondary system in pressurized water reactor (PWR) nuclear power plants. Most of iron corrosion products are generated on carbon steel materials due to flow accelerated corrosion (FAC). The several parameters like water chemistry, temperature, hydrodynamic, and steel composition affect FAC. It is well established that the at-temperature pH of the deaerated water system has a first order effect on the FAC rate of carbon steels through nuclear industry researches. In order to reduce transportation and deposition of iron corrosion products, increasing pH(t) tests were applied on secondary system of A, B units. Increasing pH(t) successfully reduced flow accelerated corrosion. The effect of increasing pH(t) to inhibit FAC was identified through the experiment and pH(t) evaluation in this paper

Activation of the IFMIF Lithium Loop Corrosion Products

Energy Technology Data Exchange (ETDEWEB)

Cambi, G [Department of Physics, Bologna University, Via Irnerio 46, 40126 Bologna (Italy); Cepraga, D G [ENEA FIS-MET, Via Don Fiammelli 2, 40128 Bologna (Italy); Frisoni, M [Athena s.a.s., Via del Battiferro 3, 40129 Bologna (Italy); Pinna, T [Associazione EURATOM- ENEA sulla Fusione, Via Enrico Fermi 45, I-00044 Frascati (RM), (Italy)

2006-07-01

The assessment of the activation of steel corrosion products generated in one year of IFMIF lithium loop operation due to the interaction between lithium and Stainless Steel SS-304 has been performed. This paper is mainly focused on the neutron activation and it describes the approach used for and present the results obtained. A preliminary estimate of the accelerator deuteron beam contribute to the activation is also presented. The study was accomplished through the following phases: 1) neutron spectrum calculation in the lithium target via MCNP-4C2 with McEnea neutron source model based on the measurements of neutron emission spectra produced in Li(d,n) reactions for a thick lithium target performed at the '' Cyclotron and Radioisotope Center (CYRIC) '', Tohoku University, Japan; 2) inventories calculations and decay gamma sources production via ANITA-IEAF activation code package; the calculations were performed by considering a lithium mix composition containing lithium impurities and corrosion products referred to 200 wppm of Steel SS-304 corresponding to a corrosion rate of 0.2 {mu}m/y and a SS-304 wetted surface of 572 m{sup 2} ; an irradiation scenario reproducing the integrated (in eleven months of operation) neutron flux responsible for the activation of the circulating corrosion products facing the deuteron beam was considered; 3) decay gamma transport analysis for dose rate evaluations via both VITENEA-IEF/SCALENEA-1 and MCNP-4C2 systems for the Longest Pipe of the Lithium loop. The following conclusions can be drawn by the results analysis: {center_dot} dose rates at 50 cm from the Longest Pipe are 198 {mu}Sv/h and 85{mu}Sv/h at 1 day and 1 week from the plant shutdown, respectively {center_dot} considering the average 20 mSv/a regulatory limit in Europe for '' Radiation Worker '' and the four-week period of annual maintenance activities in Li loop, the zone around the piping, exceeding 125 mSv/h, has to be declared '' Restricted Access Area '' {center

Activation of the IFMIF Lithium Loop Corrosion Products

International Nuclear Information System (INIS)

Cambi, G.; Cepraga, D.G.; Frisoni, M.; Pinna, T.

2006-01-01

The assessment of the activation of steel corrosion products generated in one year of IFMIF lithium loop operation due to the interaction between lithium and Stainless Steel SS-304 has been performed. This paper is mainly focused on the neutron activation and it describes the approach used for and present the results obtained. A preliminary estimate of the accelerator deuteron beam contribute to the activation is also presented. The study was accomplished through the following phases: 1) neutron spectrum calculation in the lithium target via MCNP-4C2 with McEnea neutron source model based on the measurements of neutron emission spectra produced in Li(d,n) reactions for a thick lithium target performed at the '' Cyclotron and Radioisotope Center (CYRIC) '', Tohoku University, Japan; 2) inventories calculations and decay gamma sources production via ANITA-IEAF activation code package; the calculations were performed by considering a lithium mix composition containing lithium impurities and corrosion products referred to 200 wppm of Steel SS-304 corresponding to a corrosion rate of 0.2 μm/y and a SS-304 wetted surface of 572 m 2 ; an irradiation scenario reproducing the integrated (in eleven months of operation) neutron flux responsible for the activation of the circulating corrosion products facing the deuteron beam was considered; 3) decay gamma transport analysis for dose rate evaluations via both VITENEA-IEF/SCALENEA-1 and MCNP-4C2 systems for the Longest Pipe of the Lithium loop. The following conclusions can be drawn by the results analysis: · dose rates at 50 cm from the Longest Pipe are 198 μSv/h and 85μSv/h at 1 day and 1 week from the plant shutdown, respectively · considering the average 20 mSv/a regulatory limit in Europe for '' Radiation Worker '' and the four-week period of annual maintenance activities in Li loop, the zone around the piping, exceeding 125 mSv/h, has to be declared '' Restricted Access Area '' · the worker radiation protection

75 FR 55745 - Corrosion-Resistant Carbon Steel Flat Products From the Republic of Korea: Preliminary Results...

Science.gov (United States)

2010-09-14

... Products covered by this order are certain corrosion-resistant carbon steel flat products from Korea. These... DEPARTMENT OF COMMERCE International Trade Administration [C-580-818] Corrosion-Resistant Carbon... review of the countervailing duty (CVD) order on corrosion-resistant carbon steel flat products (CORE...

Spectral Analysis of CO2 Corrosion Product Scales on 13Cr Tubing Steel

International Nuclear Information System (INIS)

Guan-fa, Lin; Zhen-quan, Bai; Yao-rong, Feng; Xun-yuan, Xu

2008-01-01

CO 2 corrosion product scales formed on 13 Cr tubing steel in autoclave and in the simulated corrosion environment of oil field are investigated in the paper. The surface and cross-section profiles of the scales were observed by scanning electron microscopy (SEM), the chemical compositions of the scales were analyzed using energy dispersion analyzer of X-ray (EDAX), X-ray diffraction (XRD) and X-ray photoelectron spectroscopy (XPS) to confirm the corrosion mechanism of the 13 Cr steel in the simulated CO 2 corrosion environment. The results show that the corrosion scales are formed by the way of fashion corrosion, consist mainly of four elements, i.e. Fe, Cr, C and O, and with a double-layer structure, in which the surface layer is constituted of bulky and incompact crystals of FeCO 3 , and the inner layer is composed of compact fine FeCO 3 crystals and amorphous Cr(OH) 3 . Because of the characteristics of compactness and ionic permeating selectivity of the inner layer of the corrosion product scales, 13 Cr steel is more resistant in CO 2 corrosion environment

In-situ investigations of corrosion processes on glass and metal surfaces by scanning probe microscopy (SPM)

International Nuclear Information System (INIS)

Nicolussi-Leck, G.

1996-09-01

The corrosion of potash-lime-silica glass was observed in-situ by AFM (atomic force microscopy) for the first time. The topographic changes with time due to the interaction of a replica glass with the ambient atmosphere were studied. A comparison of dynamic mode AFM and static mode AFM has demonstrated their potential for the investigation of soft, sensitive specimens. A combination of both methods yielded a correlation between structural changes during the corrosion process and different corrosion products on glass. The activation of surface reactions by the tip touching the surface could be observed with dynamic mode AFM. In-situ sample preparation and introduction of a defined atmosphere consisting of nitrogen with adjustable amounts of relative humidity and varying contents of SO 2 and NO 2 allowed model studies of the atmospheric corrosion. A replica glass with medieval composition was used in order to investigate the impact of the above described conditions. Besides the influence of the relative humidity the effects of SO 2 and NO 2 as well as their, synergistic effects could be studied. The evaluation of the phase signal in dynamic mode AFM in addition to the topographic information allowed the identification of humid domains in and on corrosion products, respectively. The observed contrast and thus the adhesion forces, are mainly related to the different water coverage of the surface regions or the hydroscopic properties, respectively. Furthermore, the topographic changes of copper-nickel, and palladium surfaces exposed to humidified nitrogen with SO 2 have been observed in-situ. Contrary to the assumption of the metal surfaces being covered by a homogeneous layer of corrosion products, distinct clusters of products could be observed. In case of different kinds of products these clusters were arranged adjacent to each other rather than in different stacked layers. (author)

A Study on the Effect of Electrolyte Thickness on Atmospheric Corrosion of Carbon Steel

International Nuclear Information System (INIS)

Chung, Kyeong Woo; Kim, Kwang Bum

1998-01-01

Effect of electrolyte layer thickness and increase in concentration of electrolyte during electrolyte thining on the atmospheric corrosion of carbon steel were investigated using EIS and cathodic polarization technique. The electrolyte layer thickness was controlled via two methods : one is mechanical method with microsyringe applying a different amount of electrolyte onto the metal surface to give different electrolyte thickness with the same electrolyte concentration. The other is drying method in which water layer thickness decreases through drying, causing increase in concentration of electrolyte during electrolyte thinning. In the region whose corrosion rate is controlled by cathodic reaction, corrosion rate for mechanical method is larger than that for drying method. However, for the electrolyte layers thinner than 20 ∼ 30 m, increase in concentration of electrolyte cause a higher corrosion rate for the case of the mechanical method compared with that of drying method. For a carbon steel covered with 0.1M Na 2 SO 4 , maximum corrosion rate is found at an electrolyte thickness of 45 ∼ 55 μm for mechanical method. However, maximum corrosion rate is found at an electrolyte thickness of 20 ∼ 35 μm for drying method. The limiting current is inversely proportional to electrolyte thickness for electrolyte thicker than 20 ∼ 30 μm. However, further decrease of the electrolyte thickness leads to an electrolyte thickness-independent limiting current reagion, where the oxygen rate is controlled by the solvation of oxygen at the electrolyte/gas interface. Diffusion limiting current for drying method is smaller compared with that for mechanica control. This can be attributed to decreasing in O 2 solubility caused by increase in concentration of electrolyte during electrolyte thining

Corrosion of metallic materials. Dry corrosion, aqueous corrosion and corrosion by liquid metal, methods of protection

International Nuclear Information System (INIS)

Helie, Max

2015-01-01

This book is based on a course on materials given in an engineering school. The author first gives an overview of metallurgy issues: metallic materials (pure metals, metallic alloys), defects of crystal lattices (point defects, linear defects or dislocations), equilibrium diagrams, steels and cast, thermal processing of steels, stainless steels, aluminium and its alloys, copper and its alloys. The second part addresses the properties and characterization of surfaces and interfaces: singularity of a metal surface, surface energy of a metal, energy of grain boundaries, adsorption at a material surface, metal-electrolyte interface, surface oxide-electrolyte interface, techniques of surface analysis. The third chapter addresses the electrochemical aspects of corrosion: description of the corrosion phenomenon, free enthalpy of a compound and free enthalpy of a reaction, case of dry corrosion (thermodynamic aspect, Ellingham diagram, oxidation mechanisms, experimental study, macroscopic modelling), case of aqueous corrosion (electrochemical thermodynamics and kinetics, experimental determination of corrosion rate). The fourth part addresses the different forms of aqueous corrosion: generalized corrosion (atmospheric corrosion, mechanisms and tests), localized corrosion (galvanic, pitting, cracking, intergranular, erosion and cavitation), particular cases of stress cracking (stress corrosion, fatigue-corrosion, embrittlement by hydrogen), and bi-corrosion (of non alloyed steels, of stainless steels, and of aluminium and copper alloys). The sixth chapter addresses the struggle and the protection against aqueous corrosion: methods of prevention, scope of use of main alloys, geometry-based protection of pieces, use of corrosion inhibitors, use of organic or metallic coatings, electrochemical protection. The last chapter proposes an overview of corrosion types in industrial practices: in the automotive industry, in the oil industry, in the aircraft industry, and in the

Corrosion Measurements by Titration, (CMT). Alone or Combined With Electrochemical Measurements(EC). Examples: Corrosion of Zinc, Nickel, Aluminium and Iron

DEFF Research Database (Denmark)

Bech-Nielsen, Gregers

1998-01-01

rate (EC) can be made, at intervals, during a recording of CMT measurements, and by comparison of the two kinds of measurements possible differences can be interpreted in terms of such phenomena as metal disintegration during corrosion (chunk effects), effects of dissolution of low valence metal...... measurements should be recognized: Non-buffer solutions at pH values between 3 and 9 are preferable, an atmosphere free of acid or alkaline components is required, and deposition of corrosion products as hydroxides or carbonates should be excluded....

Corrosion of tinplate T54S and T61 in humid atmosphere and saline solution

Energy Technology Data Exchange (ETDEWEB)

Zhu, X.; Sandenbergh, R.F. [Dept. of Materials Science and Metallurgical Engineering, Univ. of Pretoria (South Africa)

2001-09-01

The initial corrosion mechanism and corrosion behaviors of tinplate T54S and T61 were investigated by chemical stripping layer by layer, humid atmosphere exposure, SEM and potentiodynamic method in saline solutions with the addition of a small amount of components simulating foods and tomato sauce. The results show that T54S initially corroded in the form of pitting at the bottom of grease marks on the surface while T61 displayed the initial corrosion along the steel base on the interface of the tin coating and steel, and both were driven by galvanic corrosion between tin coating as a cathode and base steel as an anode. In the solution of 3.5% NaCl, the free corrosion potential from the outer layer to steel base shifted to negative with an addition of 100 ppm HNO{sub 3} but the potential order reversed as HNO{sub 2} replaced HNO{sub 3} at equivalent content. With an addition of 100 ppm NaHS, a high cathodic peak for either the middle or the inner layers was ascribed to the involvement of the reduction of extra hydrogen, i.e. HS{sup -}. T54S displayed a wider anodic passive zone and lower passive current density than T61, which resulted from the effect of the alloy layer. (orig.)

Investigations of the diverse corrosion products on steel in a hydrogen sulfide environment

International Nuclear Information System (INIS)

Bai, Pengpeng; Zheng, Shuqi; Zhao, Hui; Ding, Yu; Wu, Jian; Chen, Changfeng

2014-01-01

Highlights: • Diverse corrosion products on steel are investigated in H 2 S environment. • The sequence of the main corrosion products is mackinawite + cubic FeS → troilite. • The large single beam-shaped troilite has a growth pattern along the c axis. • The flower-like troilite develops from beam- or hexagonal wire-shaped grains. • The corresponding crystal structure and morphology of the products are provided. - Abstract: The corrosion products of carbon steel in aqueous H 2 S environment are investigated. The products, which include mackinawite, cubic FeS, troilite, and pyrite, are characterized through their shapes, chemical compositions and crystal structures. Mackinawite appears with a flake shape. Cubic FeS has a perfect/truncated octahedral shape, and pyrite is framboid-shaped. Flower-shaped troilite is developed from beam- or hexagonal wire-shaped grains by electrostatic interactions along a certain lattice plane. The large single beam-shaped troilite has a growth pattern along the c axis. The corresponding crystal structure and micro-morphology of the corrosion products are provided, and the three-dimensional models of them are generated

Methodology for the accelerated simulation of the deterioration that by atmospheric corrosion appears in electronic equipment; Metodologia para la simulacion acelerada del deterioro que por corrosion atmosferica se presenta en equipo electronico

Energy Technology Data Exchange (ETDEWEB)

Ortiz Prado, A.; Schouwenaars, R.; Cerrud Sanchez, S.M. [Facultad de Ingenieria, UNAM, Mexico, D.F. (Mexico)

2002-12-01

The corrosion resistance of systems and electronic parts which are designed to work in atmospheric conditions have been tested for decades; some of these methods were the Cyclic Humidity Test, Field Tests and Salt Spray (Fog) Testing, the latter was one of the most popular methods. However, the salt spray test and most of the other existing methods do not show strong relationships with the real conditions of service. For this reason, it is necessary to develop appropriated methods and equipment for the accelerated simulation of real atmospheric corrosion phenomena. This article seeks to demonstrate the need to develop a test and the necessary equipment to reproduce the damage in electronic systems and equipment by atmospheric corrosion. [Spanish] Para la evaluacion de la resistencia a la corrosion de sistemas y equipo electronico que trabajaran bajo condiciones de deterioro generadas por el medio ambiente, se han aplicado una serie de ensayos, donde el mas popular es el de camara de niebla salina. Sin embargo, este y otros que se han elaborado para tal efecto no tienen ninguna relacion con las condiciones reales de servicio, por lo que es necesario un metodo de evaluacion que permita simular de forma acelerada los fenomenos de deterioro por efectos ambientales. Este articulo pretende demostrar la necesidad de desarrollar una prueba, que en forma acelerada, reproduzca el dano que sufre el material por efecto de la atmosfera; el cual se orienta a la evaluacion de equipo electrico y electronico.

Correlation between the surface chemistry and the atmospheric corrosion of AZ31, AZ80 and AZ91D magnesium alloys

International Nuclear Information System (INIS)

Feliu, S.; Pardo, A.; Merino, M.C.; Coy, A.E.; Viejo, F.; Arrabal, R.

2009-01-01

X-ray photoelectron spectroscopy (XPS) was used in order to investigate the correlation between the surface chemistry and the atmospheric corrosion of AZ31, AZ80 and AZ91D magnesium alloys exposed to 98% relative humidity at 50 deg. C. Commercially pure magnesium, used as the reference material, revealed MgO, Mg(OH) 2 and tracers of magnesium carbonate in the air-formed film. For the AZ80 and AZ91D alloys, the amount of magnesium carbonate formed on the surface reached similar values to those of MgO and Mg(OH) 2 . A linear relation between the amount of magnesium carbonate formed on the surface and the subsequent corrosion behaviour in the humid environment was found. The AZ80 alloy revealed the highest amount of magnesium carbonate in the air-formed film and the highest atmospheric corrosion resistance, even higher than the AZ91D alloy, indicating that aluminium distribution in the alloy microstructure influenced the amount of magnesium carbonate formed.

Design considerations of fission and corrosion product in primary system of MONJU

International Nuclear Information System (INIS)

Yanagisawa, T.; Akagane, K.; Yamamoto, K.; Kawashima, K.

1976-01-01

General influence of fission and corrosion products in primary system on MONJU plant design is reviewed. Various research and development works are now in progress to decrease the generation rate, to remove the products more effectively and to develop the methods of evaluation the behaviour of radioactive products. The inventory and distribution of fission and corrosion products in the primary circuit of MONJU are given. The radiation levels on the primary components are estimated to be several roentgens per hour. (author)

Mechanical properties of layers of corrosion products at steel / concrete interface

International Nuclear Information System (INIS)

Dehoux, Anita

2012-01-01

To take account of the development of corrosion products layers in residual lifetime calculations of reinforced concrete structures requires a good knowledge of the mechanical properties of these products. Our study aims to determine the mechanical properties of layers of corrosion products. The approach consists of an identification of the microstructure properties complemented by homogenization calculations to calculate a mesoscopic behavior in linear elasticity of layers of corrosion products. The study includes a series of experimental campaigns at the microscopic scale. Vickers micro indentation tests analyzed by a Gaussian mixture model approach allowed the acquisition of hardness and elastic moduli at the microscale. An identification of the microstructure products is performed by Raman microspectrometry. The microstructure's characterization brings valuable information for homogenization calculations. The first approach has consisted of calculations of random media homogenization by self-consistent and generalized self-consistent schemes. In the second approach, effective modulus calculations were performed using numerical microstructures resulting from 2D images taken with an optical microscope. The corpus is composed of samples of different ages and origins, their microstructures were compared. (author) [fr

Spatial distribution of crystalline corrosion products formed during corrosion of stainless steel in concrete

KAUST Repository

Serdar, Marijana

2015-05-01

© 2015 Elsevier Ltd All rights reserved. The mineralogy and spatial distribution of nano-crystalline corrosion products that form in the steel/concrete interface were characterized using synchrotron X-ray micro-diffraction (μ-XRD). Two types of low-nickel high-chromium reinforcing steels embedded into mortar and exposed to NaCl solution were investigated. Corrosion in the samples was confirmed by electrochemical impedance spectroscopy (EIS). μ-XRD revealed that goethite (α-FeOOH) and akaganeite (β-FeOOH) are the main iron oxide-hydroxides formed during the chloride-induced corrosion of stainless steel in concrete. Goethite is formed closer to the surface of the steel due to the presence of chromium in the steel, while akaganeite is formed further away from the surface due to the presence of chloride ions. Detailed microstructural analysis is shown and discussed on one sample of each type of steel.

Spatial distribution of crystalline corrosion products formed during corrosion of stainless steel in concrete

KAUST Repository

Serdar, Marijana; Meral, Cagla; Kunz, Martin; Bjegovic, Dubravka; Wenk, Hans-Rudolf; Monteiro, Paulo J.M.

2015-01-01

© 2015 Elsevier Ltd All rights reserved. The mineralogy and spatial distribution of nano-crystalline corrosion products that form in the steel/concrete interface were characterized using synchrotron X-ray micro-diffraction (μ-XRD). Two types of low-nickel high-chromium reinforcing steels embedded into mortar and exposed to NaCl solution were investigated. Corrosion in the samples was confirmed by electrochemical impedance spectroscopy (EIS). μ-XRD revealed that goethite (α-FeOOH) and akaganeite (β-FeOOH) are the main iron oxide-hydroxides formed during the chloride-induced corrosion of stainless steel in concrete. Goethite is formed closer to the surface of the steel due to the presence of chromium in the steel, while akaganeite is formed further away from the surface due to the presence of chloride ions. Detailed microstructural analysis is shown and discussed on one sample of each type of steel.

STEEL CORROSION AT 600°C IN SINGLE AND DUAL CONDITION IN OXYFUEL ATMOSPHERE

Directory of Open Access Journals (Sweden)

Daniel Massari de Souza Coelho

2014-10-01

Full Text Available Coal-fired power plants using the Oxyfuel process are being developed to produce electricity with zero CO2 emission. Steels used in this and other processes are often exposed to different atmospheres in each side of the material, especially in heat exchangers and solid oxide fuel cells. Some studies have shown that steels exposed to different hydrogen partial pressures in each side have a different corrosion behavior from steels exposed to a single atmosphere condition. In this investigation, two experimental steels were studied at 600°C and 1 atm in dual atmospheres containing water vapor in one side and flue gas in the other and they were compared to steels oxidized in single atmospheres. The gas composition used is similar to the ones found in Oxyfuel coal power plants, where there is a great concentration of CO2, and also H2O and SO2. Analyses were made using SEM and TEM.

Material selection and corrosion control practices in petroleum production

International Nuclear Information System (INIS)

Tuttle, R.N.

1980-01-01

The intent of this paper is to review briefly the current state of the art and to discuss some of the anticipated future oil and gas drilling and production activities which may challenge the materials selection and corrosion technologies. The current state of art discussions in this paper have been augmented by providing a list of references so that interested engineers may delve into each subject in more detail as desired. The technological areas which appear to require additional input to meet future needs include high strength tubular goods for sour gas service, corrosion resistant high strength alloys, definition of the effects of pressure, temperature, and fluid composition on corrosion behavior, and fatigue properties of various steels in seawater

Atmospheric corrosion of low carbon steel in a polar marine environment. Study of the effect of wind regime; Corrosion atmosferica del acero bajo en carbono en un ambiente marino polar. Estudio del efecto del regimen de vientos

Energy Technology Data Exchange (ETDEWEB)

Rivero, S.; Chico, B.; Fuente, D. de la; Morcillo, M.

2007-07-01

The present work studies the atmospheric corrosion of carbon steel (UNE-EN 10130) in a sub-polar marine environment (Artigas Antarctic Scientific Base (BCAA), Uruguay) as a function of site atmospheric salinity and exposure time. A linear relationship is established between corrosion rate and airborne salinity deposition rate, valid in the deposition range encountered (125-225 mg Cl-l/m{sup 2}.d) and a bi logarithmic relationship established between corrosion and exposure time (1-4 years). Atmospheric salinity is related with the monthly wind speed average, based on the concept of the wind run. chloride ion deposition rates of less than 300 mg Cl-l/m{sup 2}.d are related with remote (oceanic) winds and coastal winds basically of speeds between 1-40 km/h, while higher deposition rates (300-700 mg Cl-/m{sup 2}.d) correspond to coastal marine winds of a certain persistence with speeds of between 41-80 km/h. (Author) 39 refs.

Corrosion control for low-cost reliability

International Nuclear Information System (INIS)

Anon.

1993-01-01

This conference was held September 19-24, 1993 in Houston, Texas to provide a forum for exchange of state-of-the-art information on corrosion. Topics of interest focus on the following: atmospheric corrosion; chemical process industry corrosion; high temperature corrosion; and corrosion of plant materials. Individual papers have been processed separately for inclusion in the appropriate data bases

Phase Analysis of Corrosion Products from Nuclear Power Plants

International Nuclear Information System (INIS)

Lipka, J.; Slugen, V.; Toth, I.; Hascik, J.; Lehota, M.

2002-01-01

The variability of the properties and the composition of the corrosion products of the stainless CrNi and mild steels in dependence on the conditions (temperature, acidity, etc.) is of such a range that, in practice, it is impossible to determine the properties of the corrosion products for an actual case from the theoretical data only. Since the decontamination processes for the materials of the water-cooled reactor (VVER-440) secondary circuits are in a process of development, it is necessary to draw the needed information by the measurement and analysis of the real specimens. The corrosion layer was separated by scraping the rust off the surface and the powder samples were studied by transmission Moessbauer spectroscopy. It should be noted that the gamma spectroscopic measurements give no evidence of the presence of low-energy gamma radiation emitted from the samples. The scrapped specimen powder was homogenised (using the 50 μm sieve) and fixed into the special holder. The 57 Co in Rh matrix was used as the radioactive Moessbauer source. Measured spectra were fitted using program NORMOS SITE. According to the results obtained from Moessbauer spectra, it is possible to establish that the main component of secondary circuit's corrosion products is magnetite Fe 3 O 4 . Next components are hematite α-Fe 2 O 3 and hydroxide akagenite β-FeOOH, which is characterised by a significant paramagnetic doublet in the middle of the spectra. The sextets corresponding to base materials (martensite and austenite steels) were identified in all measured spectra.

Corrosion of copper-based materials in irradiated moist air systems

International Nuclear Information System (INIS)

Reed, D.T.; Van Konynenburg, R.A.

1991-06-01

The atmospheric corrosion of oxygen-free copper (CDA-102), 70/30 copper-nickel (CDA-715), and 7% aluminum bronze (CDA-613) in an irradiated moist air environment was investigated. Experiments were performed in both dry and 40% RH (at sign 90 degree C) air at temperatures of 90 and 150 degree C. Initial corrosion rates were determined based on a combination of weight gain and weight loss measurements. Corrosion products observed were identified. These experiments support efforts by the Yucca Mountain Project (YMP) to evaluate possible metallic barrier materials for nuclear waste containers. 8 refs., 1 fig., 2 tabs

Sulphide production and corrosion in seawaters during exposure to FAME diesel.

Science.gov (United States)

Lee, Jason S; Ray, Richard I; Little, Brenda J; Duncan, Kathleen E; Oldham, Athenia L; Davidova, Irene A; Suflita, Joseph M

2012-01-01

Experiments were designed to evaluate the corrosion-related consequences of storing/transporting fatty acid methyl ester (FAME) alternative diesel fuel in contact with natural seawater. Coastal Key West, FL (KW), and Persian Gulf (PG) seawaters, representing an oligotrophic and a more organic- and inorganic mineral-rich environment, respectively, were used in 60 day incubations with unprotected carbon steel. The original microflora of the two seawaters were similar with respect to major taxonomic groups but with markedly different species. After exposure to FAME diesel, the microflora of the waters changed substantially, with Clostridiales (Firmicutes) becoming dominant in both. Despite low numbers of sulphate-reducing bacteria in the original waters and after FAME diesel exposure, sulphide levels and corrosion increased markedly due to microbial sulphide production. Corrosion morphology was in the form of isolated pits surrounded by an intact, passive surface with the deepest pits associated with the fuel/seawater interface in the KW exposure. In the presence of FAME diesel, the highest corrosion rates measured by linear polarization occurred in the KW exposure correlating with significantly higher concentrations of sulphur and chlorine (presumed sulphide and chloride, respectively) in the corrosion products.

Enhanced corrosion resistance and hemocompatibility of biomedical NiTi alloy by atmospheric-pressure plasma polymerized fluorine-rich coating

Energy Technology Data Exchange (ETDEWEB)

Li, Penghui; Li, Limin [Department of Physics and Materials Science, City University of Hong Kong, Tat Chee Avenue, Kowloon, Hong Kong (China); Wang, Wenhao [Department of Physics and Materials Science, City University of Hong Kong, Tat Chee Avenue, Kowloon, Hong Kong (China); Division of Spine Surgery, Department of Orthopaedics and Traumatology, Pokfulam, Hong Kong (China); Jin, Weihong [Department of Physics and Materials Science, City University of Hong Kong, Tat Chee Avenue, Kowloon, Hong Kong (China); Liu, Xiangmei [Department of Physics and Materials Science, City University of Hong Kong, Tat Chee Avenue, Kowloon, Hong Kong (China); Ministry of Education Key Laboratory for the Green Preparation and Application of Functional Materials, Hubei University, Wuhan, Hubei 430062 (China); Yeung, Kelvin W.K. [Division of Spine Surgery, Department of Orthopaedics and Traumatology, Pokfulam, Hong Kong (China); Chu, Paul K., E-mail: paul.chu@cityu.edu.hk [Department of Physics and Materials Science, City University of Hong Kong, Tat Chee Avenue, Kowloon, Hong Kong (China)

2014-04-01

Highlights: • Fluoropolymer is deposited on NiTi alloy via atmospheric-pressure plasma polymerization. • The corrosion resistance of NiTi alloy in SBF and DMEM is evidently improved. • The adsorption ratio of albumin to fibrinogen is increased on the coated surface. • The reduced platelet adhesion number indicates better in vitro hemocompatibility. - Abstract: To improve the corrosion resistance and hemocompatibility of biomedical NiTi alloy, hydrophobic polymer coatings are deposited by plasma polymerization in the presence of a fluorine-containing precursor using an atmospheric-pressure plasma jet. This process takes place at a low temperature in air and can be used to deposit fluoropolymer films using organic compounds that cannot be achieved by conventional polymerization techniques. The composition and chemical states of the polymer coatings are characterized by fourier transform infrared spectroscopy (FTIR) and X-ray photoelectron spectroscopy (XPS). The corrosion behavior of the coated and bare NiTi samples is assessed and compared by polarization tests and electrochemical impedance spectroscopy (EIS) in physiological solutions including simulated body fluids (SBF) and Dulbecco's Modified Eagle's medium (DMEM). The corrosion resistance of the coated NiTi alloy is evidently improved. Protein adsorption and platelet adhesion tests reveal that the adsorption ratio of albumin to fibrinogen is increased and the number of adherent platelets on the coating is greatly reduced. The plasma polymerized coating renders NiTi better in vitro hemocompatibility and is promising as a protective and hemocompatible coating on cardiovascular implants.

In situ Raman identification of corrosion products on galvanized steel sheets

International Nuclear Information System (INIS)

Bernard, M.C.; Hugot le Goff, A.; Massinon, D.; Phillips, N.; Thierry, D.

1992-01-01

In situ Raman spectroscopy was used to identify corrosion products on zinc immersed in chloride solutions. In aerated 0,03 M NaCl solution, zinc carbonate was identified as the main corrosion product. Even with higher chloride concentrations, for which zinc hydroxychloride was also detected, the carbon dioxide concentration is likely to be the rate controlling factor of the corrosion process. In a confinement experiment, Raman analysis revealed that the upper face of the sample was covered with zinc carbonate, whereas hydroxychlorides were identified on the confined face. This result confirmed the hypothesis of a differential aeration mechanism responsible for the formation of zinc hydroxychloride. This is in good agreement with Raman spectroscopy results obtained in the case of painted galvanized steel

The effects of corrosion product colloids on actinide transport

International Nuclear Information System (INIS)

Gardiner, M.P.; Smith, A.J.; Williams, S.J.

1991-11-01

This report assesses the possible effects of colloidal corrosion products on the transport of actinides from the near field of radioactive waste repositories. The desorption of plutonium and americium from colloidal corrosion products of iron and zirconium was studied under conditions simulating a transition from near-field to far-field environmental conditions. Desorption of actinides occurred slowly from the colloids under far-field conditions. Measurements of particle stability showed all the colloids to be unstable in the near field. Stability increased under far-field conditions or as a result of the evolution of the near field. Migration of colloids from the near field is unlikely except in the presence of organic materials. (Author)

Corrosivity Index Copper and Steel at Two Locations in Villahermosa, Tabasco

Directory of Open Access Journals (Sweden)

Tejero-Rivas María Candelaria

2015-03-01

Full Text Available This paper presents a study of the atmospheric corrosion of copper and carbon steel made ​​in two environments Villahermosa, Tabasco for six months. The test site of the industrial zone started Villahermosa Institute of Technology (ITVH and rural-urban site at the Technological University of Tabasco (UTTAB. Aluminum in combination with a screw carbon steel provided the index marine corrosivity (MA, the brass screw gives the index of industrial corrosivity (IA; wire method of screw according to ASTM G116-93 was used and the plastic screw nylon gives the rate of rural-urban corrosivity (RUA. The determination of air pollutants (sulfur dioxide and chlorides, was with the methods of wet candle and sulfation plates according to ISO 9225. Morphology studies were performed on the corrosion products formed on the specimens screw, using scanning electron microscopy coupled with energy dispersive. The corrosion products that formed on the surface of copper and carbon steel, having a bulb-shaped morphology characteristic of the addition of soluble salts, particularly sulphates and chlorides, were identified in the two stations.

New approach to the elucidation of corrosion mechanism of ceramics by the ion implantation

International Nuclear Information System (INIS)

Saito, J.; Hayashi, K.; Tachi, Y.; Kano, S.

1998-08-01

Ceramics possessing high temperature strength are promising materials for the structural application in severe environment. The development of ceramics has been carried out in order to use them in FBR environment such as liquid sodium. In particular, corrosion behavior of ceramics has been investigated to improve the corrosion resistance in liquid sodium. However, the corrosion mechanism of ceramics was not comprehended in detail even now. Because corrosion products which were deposited on the surface of test pieces during corrosion test and played an important role in corrosion behavior, were not detected distinctly after thr corrosion test. In this study, an ion implantation technique was applied to understand the corrosion mechanism of ceramics in stead of the conventional corrosion test. Sodium ions were implanted in ceramics (100 keV, 1.9 x 10 17 ions/cm 2 ) and then heat treatment was performed at either 923 K or 823 K for 36 ks in argon atmosphere. After that, products on the surface were analyzed using SEM and TEM observation and X-ray diffraction. Consequently, the corrosion products were not identified exactly, but their presence was confirmed on the surface. It was caused by the minute amount of corrosion products. In future, it is necessary to carry systematically out the implantation and heat treatment under various conditions. Therefore, it seems that the beneficial information will be obtained to understand the corrosion mechanism of ceramics. (author)

Corrosion and corrosion control

International Nuclear Information System (INIS)

Khanna, A.S.; Totlani, M.K.

1995-01-01

Corrosion has always been associated with structures, plants, installations and equipment exposed to aggressive environments. It effects economy, safety and product reliability. Monitoring of component corrosion has thus become an essential requirement for the plant health and safety. Protection methods such as appropriate coatings, cathodic protection and use of inhibitors have become essential design parameters. High temperature corrosion, especially hot corrosion, is still a difficult concept to accommodate in corrosion allowance; there is a lack of harmonized system of performance testing of materials at high temperatures. In order to discuss and deliberate on these aspects, National Association for Corrosion Engineers International organised a National Conference on Corrosion and its Control in Bombay during November 28-30, 1995. This volume contains papers presented at the symposium. Paper relevant to INIS is indexed separately. refs., figs., tabs

Analysis of corrosion products of carbon steel in wet bentonite

International Nuclear Information System (INIS)

Osada, Kazuo; Nagano, Tetsushi; Nakayama, Shinichi; Muraoka, Susumu

1992-02-01

As a part of evaluation of the long-term durability for the overpack containers for high-level radioactive waste, we have conducted corrosion tests for carbon steel in wet bentonite, a candidate buffer material. The corrosion rates were evaluated by weight difference of carbon steel and corrosion products were analyzed by Fourier transform infrared spectroscopy (FT-IR) and colorimetry. At 40degC, the corrosion rate of carbon steel in wet bentonite was smaller than that in pure water. At 95degC, however, the corrosion rate in wet bentonite was much higher than that in pure water. This high corrosion rate in wet bentonite at 95degC was considered to result from evaporation of moisture in bentonite in contact with the metal. This evaporation led to dryness and then to shrinkage of the bentonite, which generated ununiform contact of the metal with bentonite. Probably, this ununiform contact promoted the local corrosion. The locally corroded parts of specimen in wet bentonite at 95degC were analyzed by Fourier transform infrared microspectroscopy (micro-FT-IR), and lepidocrocite γ-FeO(OH) was found as well as goethite α-FeO(OH). In wet bentonite at 95degC, hematite α-Fe 2 O 3 was identified by means of colorimetry. (author)

Corrosion Cost and Corrosion Map of Korea - Based on the Data from 2005 to 2010

International Nuclear Information System (INIS)

Kim, Y. S.; Lim, H. K.; Kim, J. J.; Hwang, W. S.; Park, Y. S.

2011-01-01

Corrosion of metallic materials occurs by the reaction with corrosive environment such as atmosphere, marine, soil, urban, high temperature etc. In general, reduction of thickness and cracking and degradation are resulted from corrosion. Corrosion in all industrial facilities and infrastructure causes large economic losses as well as a large number of accidents. Economic loss by corrosion has been reported to be nearly 1-6% of GNP or GDP. In order to reduce corrosion damage of industrial facilities, corrosion map as well as a systematic investigation of the loss of corrosion in each industrial sector is needed. The Corrosion Science Society of Korea in collaboration with 15 universities and institutes has started to survey on the cost of corrosion and corrosion map of Korea since 2005. This work presents the results of the survey on cost of corrosion by Uhlig, Hoar, and input-output methods, and the evaluation of atmospheric corrosion rate of carbon steel, weathering steel, galvanized steel, copper, and aluminum in Korea. The total corrosion cost was estimated in terms of the percentage of the GDP of industry sectors and the total GDP of Korea. According to the result of Input/output method, corrosion cost of Korea was calculated as 2.9% to GDP (2005). Time of wetness was shown to be categories 3 to 4 in all exposure areas. A definite seasonal difference was observed in Korea. In summer and fall, time of wetness was higher than in other seasons. Because of short exposure period (12 months), significant corrosion trends depending upon materials and exposure corrosion environments were not revealed even though increased mass loss and decreased corrosion rate by exposure time

The corrosion products in the coolant circuits of pressurized water nuclear power plants

International Nuclear Information System (INIS)

Darras, R.

1983-01-01

The characteristics of the corrosion products formed in the primary and secondary coolant circuits of light-water pressurized reactors are reviewed. The problem induced by the pollution of coolants and metallic surface are examined. Then, the recommendations to follow to minimize the disturbing effects of this pollution by the corrosion products are indicated [fr

Rhenium corrosion in chloride melts

International Nuclear Information System (INIS)

Stepanov, A.D.; Shkol'nikov, S.N.; Vetyukov, M.M.

1989-01-01

The results investigating rhenium corrosion in chloride melts containing sodium, potassium and chromium ions by a gravimetry potentials in argon atmosphere in a sealing quarth cell are described. Rhenium corrosion is shown to be rather considerable in melts containing CrCl 2 . The value of corrosion rate depending on temperature is determined

A study on structural analysis of highly corrosive melts at high temperature

CERN Document Server

Ohtori, N

2002-01-01

When sodium is burned at high temperature in the atmosphere, it reacts simultaneously with H sub 2 O in the atmosphere so that it can produce high temperature melt of sodium hydroxide as a solvent. If this melt includes peroxide ion (O sub 2 sup 2 sup -), it will be a considerably active and corrosive for iron so that several sodium iron double oxides will be produced as corrosion products after the reaction with steel structures. The present study was carried out in order to investigate the ability of presence of peroxide ion in sodium hydroxide solvent at high temperature and that of identification of the several corrosion products using laser Raman spectroscopy. The measurement system with ultraviolet laser was developed simultaneously in the present work to improve the ability of the measurement at high temperature. As results from the measurements, the possibility of the presence of peroxide ion was shown up to 823K in sodium peroxide and 823K in the melt of sodium hydroxide mixed with sodium peroxide. A...

Corrosion of beryllium exposed to celotex and water

International Nuclear Information System (INIS)

Hill, M.A.; Butt, D.P.; Lillard, R.S.

1997-01-01

Celotex is a commercial rigid cellulose fiberboard product primarily used in the building construction industry. Currently celotex is being used as a packing material in AL-R8 containers. Ion chromatography of celotex packing material at Lawrence Livermore National Laboratory (LLNL) has indicated that this material contains aggressive anions, including chloride, which may accelerate corrosion. It is well known that beryllium is susceptible to pitting corrosion when exposed to chloride containing environments. Levy noted pitting in beryllium at the open circuit potential when exposed to 0.1 M NaCl solution. This investigation attempts to evaluate the potential risk of accelerated beryllium corrosion from celotex and water which may occur naturally when celotex dust comes into contact with moisture from the atmosphere

Mössbauer effect study of corrosion products from a Brazilian oil refinery

Science.gov (United States)

da Costa, M. I.; Kunrath, J. I.; Moro, J. T.; da Cunha, J. B. M.; Englert, G.; Comparsi, L. U.; Muller, I. L.

1993-04-01

Corrosion of an oil refining plant in southern Brazil is controlled by placing metallic coupons in strategic places of the unit. The amount of the corrosion products formed after two months of exposure of the coupons is then obtained by weight loss measurements. To have a better insight of these products an analysis by Conversion Electron and transmission Mössbauer spectroscopies was done on some of the coupons. This paper reports some of the findings.

The formation, composition and structure of corrosion products in CANDU nuclear power reactors

International Nuclear Information System (INIS)

Rummery, T.E.

1978-01-01

To gain a better understanding of the formation and transport of corrosion products in CANDU-PHW power reactors, and the role played by these products in the generation and subsequent fixation of radioactive species, we have examined in detail several surfaces removed from the Douglas Point Generating Station (Douglas Point, Ontario). Results are given for the surface of the primary-side of a Monel-400 boiler tube, and surfaces of carbon steel piping at the inlet and outlet of the boiler. The experimental techniques that were used included sequential acid stripping, X-ray diffractometry, scanning electron microscopy and energy dispersive X-ray spectrometry. The corrosion products on the Monel-400 were mainly nickel, copper, nickel oxide and nickel-deficient nickel ferrite and varied in composition and quantity as a function of both distance from the boiler inlet, and depth in the corrosion layer. The radioactive cobalt ( 60 Co) content was localized in 'streaks' deposited in the straight sections of the boiler tube, but distributed uniformly over the whole surface in the downstream bend section. The material covering the carbon steel surface comprised three phases: magnetite, aluminosilicate particles at the outermost surface, and a mixed cation spinel phase uniformly distributed over the surface at the corrosion film-water interface. The formation, composition and structure of the corrosion products are discussed. (author)

78 FR 55241 - Corrosion-Resistant Carbon Steel Flat Products From the Republic of Korea: Preliminary Results of...

Science.gov (United States)

2013-09-10

... merchandise covered by this Order \\2\\ is certain corrosion- resistant carbon steel flat products from Korea... DEPARTMENT OF COMMERCE International Trade Administration [C-580-818] Corrosion-Resistant Carbon... the countervailing duty (CVD) order on corrosion-resistant carbon steel flat products (CORE) from the...

Modeling of corrosion product migration in the secondary circuit of nuclear power plants with WWER-1200

Science.gov (United States)

Kritskii, V. G.; Berezina, I. G.; Gavrilov, A. V.; Motkova, E. A.; Zelenina, E. V.; Prokhorov, N. A.; Gorbatenko, S. P.; Tsitser, A. A.

2016-04-01

Models of corrosion and mass transfer of corrosion products in the pipes of the condensate-feeding and steam paths of the secondary circuit of NPPs with WWER-1200 are presented. The mass transfer and distribution of corrosion products over the currents of the working medium of the secondary circuit were calculated using the physicochemical model of mass transfer of corrosion products in which the secondary circuit is regarded as a cyclic system consisting of a number of interrelated elements. The circuit was divided into calculated regions in which the change in the parameters (flow rate, temperature, and pressure) was traced and the rates of corrosion and corrosion products entrainment, high-temperature pH, and iron concentration were calculated. The models were verified according to the results of chemical analyses at Kalinin NPP and iron corrosion product concentrations in the feed water at different NPPs depending on pH at 25°C (pH25) for service times τ ≥ 5000 h. The calculated pH values at a coolant temperature t (pH t ) in the secondary circuit of NPPs with WWER-1200 were presented. The calculation of the distribution of pH t and ethanolamine and ammonia concentrations over the condensate feed (CFC) and steam circuits is given. The models are designed for developing the calculation codes. The project solutions of ATOMPROEKT satisfy the safety and reliability requirements for power plants with WWER-1200. The calculated corrosion and corrosion product mass transfer parameters showed that the model allows the designer to choose between the increase of the correcting reagent concentration, the use of steel with higher chromium contents, and intermittent washing of the steam generator from sediments as the best solution for definite regions of the circuit.

Corrosion resistance of ceramic materials in pyrochemical reprocessing atmosphere by using molten salt for spent nuclear oxide fuel. Corrosion research under chlorine gas condition

International Nuclear Information System (INIS)

Takeuchi, Masayuki; Hanada, Keiji; Koizumi, Tsutomu; Aose, Shinichi; Kato, Toshihiro

2002-12-01

Pyrochemical reprocessing using molten salts (RIAR process) has been recently developed for spent nuclear oxide fuel and discussed in feasibility study. It is required to improve the corrosion resistance of equipments such as electrolyzer because the process is operated in severe corrosion environment. In this study, the corrosion resistance of ceramic materials was discussed through the thermodynamic calculation and corrosion test. The corrosion test was basically carried out in alkali molten salt under chlorine gas condition. And further consideration about the effects of oxygen, carbon and main fission product's chlorides were evaluated in molten salt. The result of thermodynamic calculation shows most of ceramic oxides have good chemical stability on chlorine, oxygen and uranyl chloride, however the standard Gibb's free energies with carbon have negative value. On the other hand, eleven kinds of ceramic materials were examined by corrosion test, then silicon nitride, mullite and cordierite have a good corrosion resistance less than 0.1 mm/y. Cracks were not observed on the materials and flexural strength did not reduce remarkably after 480 hours test in molten salt with Cl 2 -O 2 bubbling. In conclusion, these three ceramic materials are most applicable materials for the pyrochemical reprocessing process with chlorine gas condition. (author)

78 FR 19210 - Corrosion-Resistant Carbon Steel Flat Products From the Republic of Korea: Final Results of...

Science.gov (United States)

2013-03-29

.... Scope of the Order Products covered by this order are certain corrosion-resistant carbon steel flat... DEPARTMENT OF COMMERCE International Trade Administration [C-580-818] Corrosion-Resistant Carbon... countervailing duty (CVD) order on corrosion-resistant carbon steel flat products from the Republic of Korea for...

Hanford transuranic storage corrosion review

International Nuclear Information System (INIS)

Nelson, J.L.; Divine, J.R.

1980-12-01

The rate of atmospheric corrosion of the transuranic (TRU) waste drums at the US Department of Energy's Hanford Project, near Richland, Washington, was evaluated by Pacific Northwest Laboratory (PNL). The rate of corrosion is principally contingent upon the effects of humidity, airborne pollutants, and temperature. Results of the study indicate that actual penetration of barrels due to atmospheric corrosion will probably not occur within the 20-year specified recovery period. Several other US burial sites were surveyed, and it appears that there is sufficient uncertainty in the available data to prevent a clearcut statement of the corrosion rate at a specific site. Laboratory and site tests are recommended before any definite conclusions can be made. The corrosion potential at the Hanford TRU waste site could be reduced by a combination of changes in drum materials (for example, using galvanized barrels instead of the currently used mild steel barrels), environmental exposure conditions (for example, covering the barrels in one of numerous possible ways), and storage conditions

Corrosion products, activity transport and deposition in boiling water reactor recirculation systems

International Nuclear Information System (INIS)

Alder, H.P.; Buckley, D.; Grauer, R.; Wiedemann, K.H.

1992-01-01

The deposition of activated corrosion products in the recirculation loops of Boiling Water Reactors produces increased radiation levels which lead to a corresponding increase in personnel radiation dose during shut down and maintenance. The major part of this dose rate is due to cobalt-60. Based on a comprehensive literature study concerning this theme, it has been attempted to identify the individual stages of the activity build-up and to classify their importance. The following areas are discussed in detail: The origins of the corrosion products and of cobalt-59 in the reactor feedwaters; the consolidation of the cobalt in the fuel pins deposits (activation); the release and transport of cobalt-60; the build-up of cobalt-60 in the corrosion products in the recirculation loops. Existing models of the build-up of circuit radioactivity are discussed and the operating experiences from selected reactors are summarized. 90 refs, figs and tabs

77 FR 31877 - Corrosion-Resistant Carbon Steel Flat Products From Germany and Korea; Scheduling of Full Five...

Science.gov (United States)

2012-05-30

... INTERNATIONAL TRADE COMMISSION [Investigation Nos. 701-TA-350 and 731-TA-616 and 618 (Third Review)] Corrosion-Resistant Carbon Steel Flat Products From Germany and Korea; Scheduling of Full Five-Year Reviews... corrosion-resistant carbon steel flat products from Korea and the antidumping duty orders on corrosion...

78 FR 16832 - Corrosion-Resistant Carbon Steel Flat Products From Germany and the Republic of Korea: Revocation...

Science.gov (United States)

2013-03-19

...] Corrosion-Resistant Carbon Steel Flat Products From Germany and the Republic of Korea: Revocation of... ``ITC'') that revocation of the antidumping duty (``AD'') orders on corrosion-resistant carbon steel... (``Sunset'') Review, 77 FR 85 (January 3, 2012). \\2\\ See Corrosion-Resistant Carbon Steel Flat Products From...

Deposition of SiOx on Metal Surface with a DBD Plasma Gun at Atmospheric Pressure for Corrosion Prevention

International Nuclear Information System (INIS)

Han Erli; Chen Qiang; Zhang Yuefei; Chen Fei; Ge Yuanjing

2007-01-01

In this study, SiO x films were deposited by a dielectric barrier discharge (DBD) plasma gun at an atmospheric pressure. The relationship of the film structures with plasma powers was investigated by Fourier transform infrared spectroscopy (FTIR), and scanning electron microscope (SEM). It was shown that an uniform and cross-linking structure film was formed by the DBD gun. As an application, the SiO x films were deposited on a carbon steel surface for the anti-corrosion purpose. The experiment was carried out in a 0.1 M NaCl solution. It was found that a very good anti-corrosive property was obtained, i.e., the corrosion rate was decreased c.a. 15 times in 5% NaCl solution compared to the non-SiO x coated steel, as detected by the potentiodynamic polarization measurement

Corrosion behaviour of metallic containers during long term interim storages

International Nuclear Information System (INIS)

Desgranges, C.; Feron, D.; Mazaudier, F.; Terlain, A.

2001-01-01

Two main corrosion phenomena are encountered in long term interim storage conditions: dry oxidation by the air when the temperature of high level nuclear wastes containers is high enough (roughly higher than 100 C) and corrosion phenomena as those encountered in outdoor atmospheric corrosion when the temperature of the container wall is low enough and so condensation is possible on the container walls. Results obtained with dry oxidation in air lead to predict small damages (less than 1μm on steels over 100 years at 100 C) and no drastic changes with pollutants. For atmospheric corrosion, first developments deal with a pragmatic method that gives assessments of the indoor atmospheric corrosivities. (author)

Evaluation of hydrogen production from CO2 corrosion of steel drums in SFR, Part 2

International Nuclear Information System (INIS)

Dugstad, A.; Videm, K.

1987-06-01

An experimental program has been carried out for the investigation of the hydrogen formation due to corrosion of steel by water containing CO 2 produced by microbiologic decomposition of paper in waste drums. The hydrogen production will be limited by a limited rate of CO 2 production, as CO 2 is consumed by corrosive reactions producing carbonate containing corrosion products. Experiments indicated that also iron oxide and hydroxides were formed together with FeCO 3 at low CO 2 partial pressures but at a rate which leads to a rather slow increase in hydrogen production. Hydrogen evaluation has been overestimated in previous reports on this subject. (authors)

Molten salt corrosion behavior of structural materials in LiCl-KCl-UCl3 by thermogravimetric study

Science.gov (United States)

Rao, Ch Jagadeeswara; Ningshen, S.; Mallika, C.; Mudali, U. Kamachi

2018-04-01

The corrosion resistance of structural materials has been recognized as a key issue in the various unit operations such as salt purification, electrorefining, cathode processing and injection casting in the pyrochemical reprocessing of spent metallic nuclear fuels. In the present work, the corrosion behavior of the candidate materials of stainless steel (SS) 410, 2.25Cr-1Mo and 9Cr-1Mo steels was investigated in molten LiCl-KCl-UCl3 salt by thermogravimetric analysis under inert and reactive atmospheres at 500 and 600 °C, for 6 h duration. Insignificant weight gain (less than 1 mg/cm2) in the inert atmosphere and marginal weight gain (maximum 5 mg/cm2) in the reactive atmosphere were observed at both the temperatures. Chromium depletion rates and formation of Cr-rich corrosion products increased with increasing temperature of exposure in both inert and reactive atmospheres as evidenced by SEM and EDS analysis. The corrosion attack by LiCl-KCl-UCl3 molten salt, under reactive atmosphere for 6 h duration was more in the case of SS410 than 9Cr-1Mo steel followed by 2.25Cr-1Mo steel at 500 °C and the corrosion attack at 600 °C followed the order: 9Cr-1Mo steel >2.25Cr-1Mo steel > SS410. Outward diffusion of the minor alloying element, Mo was observed in 9Cr-1Mo and 2.25Cr-1Mo steels at both temperatures under reactive atmosphere. Laser Raman spectral analysis of the molten salt corrosion tested alloys under a reactive atmosphere at 500 and 600 °C for 6 h revealed the formation of unprotected Fe3O4 and α-as well as γ-Fe2O3. The results of the present study facilitate the selection of structural materials for applications in the corrosive molten salt environment at high temperatures.

Effects of amalgam corrosion products on human cells

Energy Technology Data Exchange (ETDEWEB)

Goldschmidt, P R; Cogen, R B; Taubman, S B [Departments of Periodontics and Pathology, University of Connecticut Health Center, Farmington, Connecticut, U.S.A.

1976-01-01

Using three independent criteria, we have found that 10/sup -4/,10/sup -6/M concentrations of ions presumably liberated from the corrosion of dental amalgam produce injurious effects on either human gingival fibroblasts or HeLa cells when the cells are grown in culture. Release of /sup 51/Cr and uptake of trypan blue dye were seen with 10/sup -5/M Hg/sup + +/ and Ag/sup +/. Inhibition of amino acid incorporation into protein-like material was seen with eluates of amalgam and with ionic solutions of most metals comprising dental amalgam. Stannous ion showed little if any cytotoxic potential. These results suggest that corrosion products of amalgam are capable of causing cellular injury or destruction.

Corrosion behavior of Ni-based structural materials for electrolytic reduction in lithium molten salt

International Nuclear Information System (INIS)

Cho, Soo Haeng; Park, Sung Bin; Lee, Jong Hyeon; Hur, Jin Mok; Lee, Han Soo

2011-01-01

In this study, the corrosion behavior of new Ni-based structural materials was studied for electrolytic reduction after exposure to LiCl-Li 2 O molten salt at 650 deg. C for 24-216 h under an oxidizing atmosphere. The new alloys with Ni, Cr, Al, Si, and Nb as the major components were melted at 1700 deg. C under an inert atmosphere. The melt was poured into a preheated metallic mold to prepare an as-cast alloy. The corrosion products and fine structures of the corroded specimens were characterized by scanning electron microscope (SEM), Energy Dispersive X-ray Spectroscope (EDS), and X-ray diffraction (XRD). The corrosion products of as cast and heat treated low Si/high Ti alloys were Cr 2 O 3 , NiCr 2 O 4 , Ni, NiO, and (Al,Nb,Ti)O 2 ; those of as cast and heat treated high Si/low Ti alloys were Cr 2 O 3 , NiCr 2 O 4 , Ni, and NiO. The corrosion layers of as cast and heat treated low Si/high Ti alloys were continuous and dense. However, those of as cast and heat treated high Si/low Ti alloys were discontinuous and cracked. Heat treated low Si/high Ti alloy showed the highest corrosion resistance among the examined alloys. The superior corrosion resistance of the heat treated low Si/high Ti alloy was attributed to the addition of an appropriate amount of Si, and the metallurgical evaluations were performed systematically.

Positive aspects issued from bio corrosion studies: from hydrogen production to biofuel cells

International Nuclear Information System (INIS)

Silva Munoz, L. de

2007-12-01

Microbially influenced corrosion or bio corrosion is a problem that generates heavy global economic losses (several billion euros per year). In spite of the progress made on the understanding of the underlying mechanisms, the complexity of the phenomenon has prevented finding definitive solutions to the problem and continues to inspire many research works. The participation in bio corrosion of catalytic mechanisms induced by weak acids was studied in this work. Another objective of the thesis has been to take advantage from catalytic phenomena found in bio corrosion research to apply them in other areas: energy production with biofuel cells or electrochemical hydrogen production in mild conditions. This work has shown that the presence of weak acids and amino acids inside bio-films could play a major role in steel bio corrosion accelerating the phenomenon through the catalysis of the water reduction reaction. The reversibility of this mechanism, discerned and proved here, could explain the corrosion increase when hydrogen is removed (bacterial consumption, agitation...). In addition, phosphates allow the production of hydrogen by electrolysis in mild pH conditions (pH 4.0 - 8.0) with an equal or better performance than those found in alkaline electrolysis. Finally, industrial materials like stainless steel and titanium could be used in the fabrication of enzymatic electrodes for biosensors or microsystems. The use of the glucose oxidase/glucose system in an aqueous fuel cell with a stainless steel cathode, allows the improvement of the cell performance thanks to the production of hydrogen peroxide that is easily reduced. Moreover, the use of materials with micro-structured surfaces like sandblasted steels deserve to be studied in detail to exploit the remarkable reactivity they present compared to smooth electrodes. (author)

Positive aspects issued from bio-corrosion studies: from hydrogen production to biofuel cells

International Nuclear Information System (INIS)

De Silva Munoz, Leonardo

2007-01-01

Microbially influenced corrosion or bio-corrosion is a problem that generates heavy global economic losses (several billion euros per year). In spite of the progress made on the understanding of the underlying mechanisms, the complexity of the phenomenon has prevented finding definitive solutions to the problem and continues to inspire many research works. The participation in bio-corrosion of catalytic mechanisms induced by weak acids was studied in this work. Another objective of the thesis has been to take advantage from catalytic phenomena found in bio corrosion research to apply them in other areas: energy production with biofuel cells or electrochemical hydrogen production in mild conditions. This work has shown that the presence of weak acids and amino acids inside bio films could play a major role in steel bio-corrosion accelerating the phenomenon through the catalysis of the water reduction reaction. The reversibility of this mechanism, discerned and proved here, could explain the corrosion increase when hydrogen is removed (bacterial consumption, agitation...). In addition, phosphates allow the production of hydrogen by electrolysis in mild ph conditions (pH 4.0 - 8.0) with an equal or better performance than those found in alkaline electrolysis. Finally, industrial materials like stainless steel and titanium could be used in the fabrication of enzymatic electrodes for biosensors or microsystems. The use of the glucose oxidase / glucose system in an aqueous fuel cell with a stainless steel cathode, allows the improvement of the cell performance thanks to the production of hydrogen peroxide that is easily reduced. Moreover, the use of materials with micro-structured surfaces like sandblasted steels deserve to be studied in detail to exploit the remarkable reactivity they present compared to smooth electrodes. (author) [fr

The external beam facility used to characterize corrosion products in metallic statuettes

International Nuclear Information System (INIS)

Rizzutto, M.A.; Tabacniks, M.H.; Added, N.; Barbosa, M.D.L.; Curado, J.F.; Santos, W.A.; Lima, S.C.; Melo, H.G.; Neiva, A.C.

2005-01-01

To open new possibilities in nuclear applied physics research, mainly for the analysis of art objects in air, an external beam facility was installed at LAMFI (Laboratorio de Analise de Materiais por Feixes Ionicos) of University of Sao Paulo. PIXE measurements were made using an XR-100CR (Si-PIN) X-ray detector pointed to the sample mounted after an approximate 11 mm air path, hence with effective beam energy of 0.9 MeV. This setup was used to characterize the corrosion products of two ethnological metallic statuettes from the African collection of the Museum of Archaeology and Etnology. PIXE analysis of the corrosion free base of one statuette showed that Cu and Zn are the main components of the alloy, while Pb is present in smaller amount. The analysis of some corrosion products showed a Zn:Cu relationship higher than that of the base, evidencing selective corrosion. The main components of the other statuette were Cu and Pb, while S and Zn were found in smaller amounts

Corrosion and hydrogen permeation of A216 Grade WCA steel in hydrothermal magnesium-containing brines

International Nuclear Information System (INIS)

Haberman, J.H.; Frydrych, D.J.; Westerman, R.E.

1988-03-01

Corrosion rates determined at 1 month in 150/degree/C brine increased with magnesium concentration. The structure of the corrosion product, as determined by x-ray diffraction, depended upon the magnesium concentration. In brines with less than 10,000 ppM magnesium, the primary corrosion product had a spinel structure characteristic of magnetite or magnesioferrite. In brines containing magnesium concentrations greater than 20,000 ppM, the primary corrosion product had the amakinite structure characteristic of a complex iron-magnesium hydroxide. The high corrosion rates observed in brines containing high magnesium concentrations suggest that the corrosion products having the amakinite structure is less protective than corrosion products having the spinel structure. Corrosion rates in high-magnesium (inclusion) brine determined over a 6-month test duration were essentially constant. Hydrogen permeation rates observed in exposing mild steel to high-Mg/sup 2/plus// brine at 150/degree/C could be potentially damaging to a mild steel waste package container. The rate of hydrogen permeation was proportional to the brine flow rate in the autoclave. Thiourea additions to the brine increased the hydrogen permeation rate; sulfate and bromide ion additions did not. The maximum gaseous hydrogen pressure attainable is not known (based on 3Fe /plus/ 4H 2 O /plus/ Fe(sub 3)O /plus/ 4H 2 , would be /approximately/900 atmospheres), and the dependence of permeation rate on temperature is not known. 8 refs., 13 figs., 3 tabs

Corrosion products, activity transport and deposition in boiling water reactor recirculation systems

International Nuclear Information System (INIS)

Alder, H.P.; Buckley, D.; Grauer, R.; Wiedemann, K.H.

1989-09-01

The deposition of activated corrosion products in the recirculation loops of Boiling Water Reactors produces increased radiation levels which lead to a corresponding increase in personnel radiation dose during shut down and maintenance. The major part of this dose rate is due to cobalt-60. The following areas are discussed in detail: - the origins of the corrosion products and of cobalt-59 in the reactor feedwaters, - the consolidation of the cobalt in the fuel pin deposits (activation), - the release and transport of cobalt-60, - the build-up of cobalt-60 in the corrosion products in the recirculation loops. Existing models of the build-up of circuit radioactivity are discussed and the operating experiences from selected reactors are summarised. Corrosion chemistry aspects of the cobalt build-up in the primary circuit have already been studied on a broad basis and are continuing to be researched in a number of centers. The crystal chemistry of chromium-nickel steel corrosion products poses a number of yet unanswered questions. There are major loopholes associated with the understanding of activation processes of cobalt deposited on the fuel pins and in the mass transfer of cobalt-60. For these processes, the most important influence stems from factors associated with colloid chemistry. Accumulation of data from different BWRs contributes little to the understanding of the activity build-up. However, there are examples that the problem of activity build-up can be kept under control. Although many details for a quantitative understanding are still missing, the most important correlations are visible. The activity build-up in the BWR recirculation systems cannot be kept low by a single measure. Rather a whole series of measures is necessary, which influences not only cobalt-60 deposition but also plant and operation costs. (author) 26 figs., 13 tabs., 90 refs

Corrosion product layers on magnesium alloys AZ31 and AZ61: Surface chemistry and protective ability

Energy Technology Data Exchange (ETDEWEB)

Feliu, S., E-mail: sfeliu@cenim.csic.es; Llorente, I.

2015-08-30

Highlights: • Surface chemistry of the corrosion product layers on magnesium alloys. • Influence of the type of alloy on the carbonate surface enrichment. • Relation between surface composition and protection properties. - Abstract: This paper studies the chemical composition of the corrosion product layers formed on magnesium alloys AZ31 and AZ61 following immersion in 0.6 M NaCl, with a view to better understanding their protective action. Relative differences in the chemical nature of the layers were quantified by X-ray photoelectron spectroscopy (XPS), scanning electron microscopy (SEM), energy dispersive analysis of X-ray (EDX) and low-angle X-ray diffraction (XRD). Corrosion behavior was investigated by Electrochemical Impedance Spectroscopy (EIS) and hydrogen evolution measurement. An inhibitive effect from the corrosion product layers was observed from EIS, principally in the case of AZ31, as confirmed by hydrogen evolution tests. A link was found between carbonate enrichment observed by XPS in the surface of the corrosion product layer, concomitant with the increase in the protective properties observed by EIS.

Corrosion product layers on magnesium alloys AZ31 and AZ61: Surface chemistry and protective ability

International Nuclear Information System (INIS)

Feliu, S.; Llorente, I.

2015-01-01

Highlights: • Surface chemistry of the corrosion product layers on magnesium alloys. • Influence of the type of alloy on the carbonate surface enrichment. • Relation between surface composition and protection properties. - Abstract: This paper studies the chemical composition of the corrosion product layers formed on magnesium alloys AZ31 and AZ61 following immersion in 0.6 M NaCl, with a view to better understanding their protective action. Relative differences in the chemical nature of the layers were quantified by X-ray photoelectron spectroscopy (XPS), scanning electron microscopy (SEM), energy dispersive analysis of X-ray (EDX) and low-angle X-ray diffraction (XRD). Corrosion behavior was investigated by Electrochemical Impedance Spectroscopy (EIS) and hydrogen evolution measurement. An inhibitive effect from the corrosion product layers was observed from EIS, principally in the case of AZ31, as confirmed by hydrogen evolution tests. A link was found between carbonate enrichment observed by XPS in the surface of the corrosion product layer, concomitant with the increase in the protective properties observed by EIS

Corrosion and pyrophoricity of ZPPR fuel plates: Implications for basin storage

International Nuclear Information System (INIS)

Totemeier, T.C.; Hayes, S.L.; Pahl, R.G.; Crawford, D.C.

1997-01-01

This paper presents the results of recent experimentation and analysis of the pyrophoric behavior of corroded Zero Power Physics Reactor (ZPPR) HEU fuel plates and the implications of these results for the handling, drying, and passivation of uranium metal fuels stored in water basins. The ZPPR plates were originally clad in 1980; crevice corrosion of the uranium metal in a dry storage environment has occurred due to the use of porous cladding end plugs. The extensive corrosion has resulted in bulging and, in some cases, breaching of the cladding over a 15 year storage period. Processing of the plates has been initiated to recover the highly enriched uranium metal and remove the storage vulnerability identified with the corroded plates, which have been shown to contain significant quantities of the pyrophoric compound uranium hydride (UH 3 ). Experiments were undertaken to determine effective passivation techniques for the corrosion product; analysis and modeling was performed to determine whether heat generated by rapid hydride re-oxidation could ignite the underlying metal plates. The results of the initial passivation experiment showed that simple exposure of the hydride-containing corrosion product to an Ar-3 vol.% O 2 environment was insufficient to fully passivate the hydride--flare-up of the product occurred during subsequent vigorous handling in air. A second experiment demonstrated that corrosion product was fully stable following grinding of the product to a fine powder in the Ar-3 vol.% O 2 atmosphere. Numerical modeling of a corroded plate indicated that ignition of the plate due to the heat from hydride re-oxidation was likely if hydride fractions in the corrosion product exceeded 30%

Modelling and numerical simulation of the corrosion product transport in the pressurised water reactor primary circuit

International Nuclear Information System (INIS)

Marchetto, C.

2002-05-01

During operation of pressurised water reactor, corrosion of the primary circuit alloys leads to the release of metallic species such as iron, nickel and cobalt in the primary fluid. These corrosion products are implicated in different transport phenomena and are activated in the reactor core where they are submitted to neutron flux. The radioactive corrosion products are afterwards present in the out of flux parts of primary circuit where they generate a radiation field. The first part of this study deals with the modelling of the corrosion: product transport phenomena. In particular, considering the current state of the art, corrosion and release mechanisms are described empirically, which allows to take into account the material surface properties. New mass balance equations describing the corrosion product behaviour are thus obtained. The numerical resolution of these equations is implemented in the second part of this work. In order to obtain large time steps, we choose an implicit time scheme. The associated system is linearized from the Newton method and is solved by a preconditioned GMRES method. Moreover, a time step auto-adaptive management based on Newton iterations is performed. Consequently, an efficient resolution has been implemented, allowing to describe not only the quasi-steady evolutions but also the fast transients. In a last step, numerical simulations are carried out in order to validate the new corrosion product transport modelling and to illustrate the capabilities of this modelling. Notably, the numerical results obtained indicate that the code allows to restore the on-site observations underlining the influence of material surface properties on reactor contamination. (author)

Corrosion products behaviour under VVER primary coolant conditions

International Nuclear Information System (INIS)

Grygar, T.; Zmitko, M.

2002-01-01

The aim of this work was to collect data on thermodynamic stability of Cr, Fe, and Ni oxides, mechanisms of hydrothermal corrosion of stainless steels and to compare the real observation with the theory. We found that the electrochemical potential and pH in PWR and VVER are close to the thermodynamic boundary between two fields of stable spinel type oxides. The ways of degradation of the passivating layers due to changes in water chemistry were considered and PWR and VVER systems were found to be potentially endangered by reductive attack. In certain VVER systems the characteristics of the passivating layer on steels and also concentration of soluble corrosion products seem to be in contradiction with the theoretical expectations. (author)

Characterization of corrosion products from Nd-Fe-B magnets used in dental prostheses

Energy Technology Data Exchange (ETDEWEB)

Saiki, Mitiko; Rogero, Sizue O.; Costa, Isolda; Dantas, Elisabeth; Oliveira, Mara C.L. [Instituto de Pesquisas Energeticas e Nucleares (IPEN), Sao Paulo, SP (Brazil)

2002-07-01

A special group of magnets composed mainly by Nd-Fe-B has been widely used in dental applications as retentive devices for overdentures, due to their strong force and compactness. Dental materials should present high corrosion resistance and be innocuous to human tissues, however, Nd-Fe-B magnets are highly susceptible to corrosion. This work presents results obtained in the elemental analysis of Nd-Fe-B magnets and their corrosion products. The corrosion products were analyzed in the extracts of culture medium where the magnets had been immersed for 10 days at 37 deg C. Elements B, Co, Fe, La, Nd, Dy, Pr, Sm, Ho, Yb and Lu were found in the magnet and the analysis of extract indicated that Co, Fe and Nd are released from the magnet to the extract. Toxicity was also investigated in this extract using the neutral red uptake cytotoxicity assay. Acknowledgements: To FAPESP and CNPq for financial support. (author)

Characterization of corrosion products from Nd-Fe-B magnets used in dental prostheses

International Nuclear Information System (INIS)

Saiki, Mitiko; Rogero, Sizue O.; Costa, Isolda; Dantas, Elisabeth; Oliveira, Mara C.L.

2002-01-01

A special group of magnets composed mainly by Nd-Fe-B has been widely used in dental applications as retentive devices for overdentures, due to their strong force and compactness. Dental materials should present high corrosion resistance and be innocuous to human tissues, however, Nd-Fe-B magnets are highly susceptible to corrosion. This work presents results obtained in the elemental analysis of Nd-Fe-B magnets and their corrosion products. The corrosion products were analyzed in the extracts of culture medium where the magnets had been immersed for 10 days at 37 deg C. Elements B, Co, Fe, La, Nd, Dy, Pr, Sm, Ho, Yb and Lu were found in the magnet and the analysis of extract indicated that Co, Fe and Nd are released from the magnet to the extract. Toxicity was also investigated in this extract using the neutral red uptake cytotoxicity assay. Acknowledgements: To FAPESP and CNPq for financial support. (author)

MODIS/Aqua Atmosphere Aeronet Subsetting Product

Data.gov (United States)

National Aeronautics and Space Administration — The MODIS/Aqua Atmosphere Aeronet Subsetting Product (MYDARNSS) consists of MODIS Atmosphere and Ancillary Products subsets that are generated over a number of...

Stress corrosion cracking of U-0.1% Cr in humid helium atmosphere

International Nuclear Information System (INIS)

Zalkind, S.; Eshkenazy, R.; Harush, S.; Halperin, D.; Moreno, D.; Abramov, E.; Venkert, A.

1994-01-01

Rivets were matched into adapted drilled holes in plates, both made of U-0.1% Cr alloy and were placed in different environments containing dry air and helium and humid air and helium for a variety of exposure times. After opening, the most significant amounts of corrosion products were detected in the specimens that stayed for three years in humid helium (5% RH) environment. Radial cracks, developed in the bore edge, were detected in the specimens. X-ray diffraction patterns of the corrosion products gave the composition of UH 3 and UO 2 . The microstructure was examined using light and electron microscopy techniques. The hydride phase that was observed, formed mainly beneath the oxide layer and penetrated into the metal matrix as needle-like forms. The formation of a lower density hydride phase, yielded in a large volume change causing the development of high stresses at the rivet-bore interface. The combination of the high stress and the weakening of the bore edge due to the presence of the brittle hydride phase led to radial crack formation around the bore edge. (orig.)

Humid-air and aqueous corrosion models for corrosion-allowance barrier material

International Nuclear Information System (INIS)

Lee, J.H.; Atkins, J.E.; Andrews, R.W.

1995-01-01

Humid-air and aqueous general and pitting corrosion models (including their uncertainties) for the carbon steel outer containment barrier were developed using the corrosion data from literature for a suite of cast irons and carbon steels which have similar corrosion behaviors to the outer barrier material. The corrosion data include the potential effects of various chemical species present in the testing environments. The atmospheric corrosion data also embed any effects of cyclic wetting and drying and salts that may form on the corroding specimen surface. The humid-air and aqueous general corrosion models are consistent in that the predicted humid-air general corrosion rates at relative humidities between 85 and 100% RH are close to the predicted aqueous general corrosion rates. Using the expected values of the model parameters, the model predicts that aqueous pitting corrosion is the most likely failure mode for the carbon steel outer barrier, and an earliest failure (or initial pit penetration) of the 100-mm thick barrier may occur as early as about 500 years if it is exposed continuously to an aqueous condition at between 60 and 70 degrees C

Estimation of elastic modulus of reinforcement corrosion products using inverse analysis of digital image correlation measurements for input in corrosion-induced cracking model

DEFF Research Database (Denmark)

Pease, Bradley Justin; Michel, Alexander; Thybo, Anna Emilie A.

2012-01-01

A combined experimental and numerical approach for estimating the elastic modulus of reinforcement corrosion products is presented. Deformations between steel and mortar were measured using digital image correlation during accelerated corrosion testing at 100 μA/cm2 (~1.16 mm/year). Measured defo...

Accelerated cyclic corrosion tests

Directory of Open Access Journals (Sweden)

Prošek T.

2016-06-01

Full Text Available Accelerated corrosion testing is indispensable for material selection, quality control and both initial and residual life time prediction for bare and painted metallic, polymeric, adhesive and other materials in atmospheric exposure conditions. The best known Neutral Salt Spray (NSS test provides unrealistic conditions and poor correlation to exposures in atmosphere. Modern cyclic accelerated corrosion tests include intermittent salt spray, wet and dry phases and eventually other technical phases. They are able to predict the material performance in service more correctly as documented on several examples. The use of NSS should thus be restricted for quality control.

Durability of bare and anodised aluminium in atmosphere of very different corrosivities. II Anodised aluminium; Durabilidad del aluminio desnudo y anodizado en atmosfera de muy diferentes corrosividades. II. Aluminio anodizado

Energy Technology Data Exchange (ETDEWEB)

Lopez, V.; Escudero, E.; Gonzalez, J. A.; Otero, E.; Morcillo, M.

2004-07-01

The behaviour of three anodic films with thicknesses of approximately 7, 17 and 28 {mu}m is studied in atmospheric exposure at 11 natural testing stations with salinity levels ranging between 2.1 and 684 mg Cl''- m''-2 d''-1. To evaluate the results, use was made of gravimetric techniques, electrochemical impedance spectroscopy (EIS), EDX microanalysis, standard quality control tests, optical microscopy and, occasionally, electron microscopy. It is shown that anodising with correct sealing is an appropriate solution for preventing localised corrosion of aluminium and conserving its appearance, even in atmospheres of high corrosivity, provided that an ill-defined minimum thickness threshold is passed. The 7 {mu}m anodic films suffer corrosion after the second annual cycle in the most aggressive environments. Corrosion, when it occurs, is localised in the form of pitting or filiform corrosion. (Author) 23 refs.

Analysis of corrosion products of carbon steel in wet bentonite

International Nuclear Information System (INIS)

Osada, K.; Nagano, T.; Kozai, N.; Nakashima, S.; Nakayama, S.; Muraoka, S.

1991-01-01

The following conclusions were obtained; (1) At 40degC, the average corrosion rate of SS41 carbon steel in wet bentonite was 0.025 mm/y. This is smaller than the value of 0.042 mm/y obtained in pure water at 40degC. However, at 95degC, the corrosion rate of SS41 carbon steel in wet bentonite was 0.27 mm/y, which is much larger than that in pure water at 95degC. (2) At 95degC, γ-FeO(OH) (lepidocrocite) was formed only in wet bentonite, and it was absent in pure water. Evaporation of moisture resulted in the formation of partial covering of bentonite, which promoted local corrosion. Consequently, γ-FeO(OH) was considered to be formed. (3) In wet bentonite at 95degC, α-Fe 2 O 3 (hematite) can be identified by means of colorimetry. The color of corrosion products is orangish, indicating the contribution of α-Fe 2 O 3 in iron hydroxides. (author)

EUROCORR 2007 - The European corrosion congress - Progress by corrosion control. Book of Abstracts

International Nuclear Information System (INIS)

2007-01-01

This book of abstracts contains lectures, workshops and posters which were held on the European Corrosion Congress 2007 in Freiburg (Germany). The main topics of the sessions and posters are: 1. Corrosion and scale inhibition; 2. Corrosion by hot gases and combustion products; 3. Nuclear corrosion; 4. Environment sensitive fracture; 5. Surface Science; 6. Physico-chemical methods of corrosion testing; 7. Marine corrosion; 8. Microbial corrosion; 9. Corrosion of steel in concrete; 10. Corrosion in oil and gas production; 11. Coatings; 12. Corrosion in the refinery industry; 13. Cathodic protection; 14. Automotive Corrosion; 15. Corrosion of polymer materials. The main topics of the workshops are: 1. High temperature corrosion in the chemical, refinery and petrochemical industries; 2. Bio-Tribocorrosion; 3. Stress corrosion cracking in nuclear power plants; 4. Corrosion monitoring in nuclear systems; 5. Cathodic protection for marine and offshore environments; 6. Self-healing properties of new surface treatments; 7. Bio-Tribocorrosion - Cost 533/Eureka-ENIWEP-Meeting; 8. Drinking water systems; 9. Heat exchangers for seawater cooling

Complementary Methods for the Characterization of Corrosion Products on a Plant-Exposed Superheater Tube

DEFF Research Database (Denmark)

Okoro, Sunday Chukwudi; Nießen, Frank; Villa, Matteo

2017-01-01

In this work, complex corrosion products on a superheater tube exposed to biomass firing were characterized by the complementary use of energy-dispersive synchrotron diffraction, electron microscopy, and energy-dispersive X-ray spectroscopy. Non-destructive synchrotron diffraction in transmission......-rich austenite phase to selective removal of Fe and Cr from the alloy, via a KCl-induced corrosion mechanism. Compositional variations were related to diffraction results and revealed a qualitative influence of the spinel cation concentration on the observed diffraction lines.......In this work, complex corrosion products on a superheater tube exposed to biomass firing were characterized by the complementary use of energy-dispersive synchrotron diffraction, electron microscopy, and energy-dispersive X-ray spectroscopy. Non-destructive synchrotron diffraction in transmission...... geometry measuring with a small gauge volume from the sample surface through the corrosion product allowed depth-resolved phase identification and revealed the presence of (Fe,Cr)2O3 and FeCr2O4. This was supplemented by microstructural and elemental analysis correlating the additional presence of a Ni...

A comparative study of accelerated tests to simulate atmospheric corrosion

International Nuclear Information System (INIS)

Assis, Sergio Luiz de

2000-01-01

In this study, specimens coated with five organic coating systems were exposed to accelerated tests for periods up to 2000 hours, and also to weathering for two years and six months. The accelerated tests consisted of the salt spray test, according to ASTM B-117; Prohesion (ASTM G 85-98 annex 5A); Prohesion combined with cyclic exposure to UV-A radiation and condensation; 'Prohchuva' a test described by ASTM G 85-98 using a salt spray with composition that simulated the acid rain of Sao Paulo, but one thousand times more concentrated, and 'Prohchuva' combined with cyclic exposure to UV-A radiation and condensation. The coated specimens were exposed with and without incision to expose the substrate. The onset and progress of corrosion at and of the exposed metallic surface, besides coating degradation, were followed by visual observation, and photographs were taken. The coating systems were classified according to the extent of corrosion protection given to the substrate, using a method based on ASTM standards D-610, D-714, D-1654 and D-3359. The rankings of the coatings obtained from accelerated tests and weathering were compared and contrasted with classification of the same systems obtained from literature, for specimens exposed to an industrial atmosphere. Coating degradation was strongly dependent on the test, and could be attributed to differences in test conditions. The best correlation between accelerated test and weathering was found for the test Prohesion alternated with cycles of exposure to UV-A radiation and condensation. (author)

Corrosion-product filtration in PWRs: Topical report

International Nuclear Information System (INIS)

Balakrishnan, P.V.; Buckley, L.P.

1988-04-01

As part of a programme on the optimization of pressurized water reactor (PWR) secondary side water treatment, laboratory-scale studies on filtration of the feedwater using materials having chemically active adsorbing surfaces were carried out. Graphite, zirconia and titania were identified, from a review of existing literature, as suitable filtration media, the last two because of their ion-exchange capability. The efficiency of filters packed with granular graphite for filtration of simulated feed train corrosion products and the pressure drop across the filters were determined as functions of filter dimensions and operating parameters at room temperature. A rough sizing of a full-flow feedwater filter using granular graphite was done on the basis of observations from the room temperature tests. Further studies are suggested at low concentrations of the corrosion product and at high temperature typical of steam generator feedwater after the high pressure heaters to derive realistic design parameters for a filter for installation in the PWR secondary circuit. Zirconia was produced in the form of spherical particles using a sol-gel process. The zirconia behaved as an anion exchanger at low pH and as a cation exchanger at high pH. Its suitability for purification of water at high temperature should be determined by futher studies. 30 refs., 16 figs., 8 tabs

77 FR 27438 - Certain Corrosion-Resistant Carbon Steel Flat Products From Korea: Final Results of Expedited...

Science.gov (United States)

2012-05-10

... DEPARTMENT OF COMMERCE International Trade Administration [C-580-818] Certain Corrosion-Resistant... order on certain corrosion-resistant carbon steel flat products (``CORE'') from the Republic of Korea.... Scope of the Order The merchandise covered by the order includes flat-rolled carbon steel products, of...

Corrosion behavior of Ni-based structural materials for electrolytic reduction in lithium molten salt

Energy Technology Data Exchange (ETDEWEB)

Cho, Soo Haeng, E-mail: nshcho1@kaeri.re.kr [Korea Atomic Energy Research Institute, 1045 Daedeokdaero Yuseong-gu, Daejeon 305-353 (Korea, Republic of); Park, Sung Bin [Korea Atomic Energy Research Institute, 1045 Daedeokdaero Yuseong-gu, Daejeon 305-353 (Korea, Republic of); Lee, Jong Hyeon, E-mail: jonglee@cnu.ac.kr [Graduate School of Green Energy Technology, Chungnam National University, 79 Daehak-ro, Yuseong-gu, Daejeon 305-764 (Korea, Republic of); Hur, Jin Mok; Lee, Han Soo [Korea Atomic Energy Research Institute, 1045 Daedeokdaero Yuseong-gu, Daejeon 305-353 (Korea, Republic of)

2011-05-01

In this study, the corrosion behavior of new Ni-based structural materials was studied for electrolytic reduction after exposure to LiCl-Li{sub 2}O molten salt at 650 deg. C for 24-216 h under an oxidizing atmosphere. The new alloys with Ni, Cr, Al, Si, and Nb as the major components were melted at 1700 deg. C under an inert atmosphere. The melt was poured into a preheated metallic mold to prepare an as-cast alloy. The corrosion products and fine structures of the corroded specimens were characterized by scanning electron microscope (SEM), Energy Dispersive X-ray Spectroscope (EDS), and X-ray diffraction (XRD). The corrosion products of as cast and heat treated low Si/high Ti alloys were Cr{sub 2}O{sub 3}, NiCr{sub 2}O{sub 4}, Ni, NiO, and (Al,Nb,Ti)O{sub 2}; those of as cast and heat treated high Si/low Ti alloys were Cr{sub 2}O{sub 3}, NiCr{sub 2}O{sub 4}, Ni, and NiO. The corrosion layers of as cast and heat treated low Si/high Ti alloys were continuous and dense. However, those of as cast and heat treated high Si/low Ti alloys were discontinuous and cracked. Heat treated low Si/high Ti alloy showed the highest corrosion resistance among the examined alloys. The superior corrosion resistance of the heat treated low Si/high Ti alloy was attributed to the addition of an appropriate amount of Si, and the metallurgical evaluations were performed systematically.

Corrosion of copper containers prior to saturation of a nuclear fuel waste disposal vault

International Nuclear Information System (INIS)

King, F.; Kolar, M.

1997-12-01

The buffer material surrounding the containers in a Canadian nuclear fuel waste disposal vault will partially desiccate as a result of the elevated temperature at the container surface. This will lead to a period of corrosion in a moist air atmosphere. Corrosion will either take the form of slow oxidation if the container surface remains dry or aqueous electrochemical corrosion if the surface is wetted by a thin liquid film. The relevant literature is reviewed, from which it is concluded that corrosion should be uniform in nature, except if the surface is wetted, in which case localized corrosion is a possibility. A quantitative analysis of the extent and rate of uniform corrosion during the unsaturated period is presented. Two bounding cases are considered: first, the case of slow oxidation in moist air following either logarithmic or parabolic oxide-growth kinetics and, second, the case of electrochemically based corrosion occurring in a thin liquid film uninhibited by the growth of corrosion products. (author)

Solubility of corrosion products of plain steel in oxygen-containing water solutions at high parameters

International Nuclear Information System (INIS)

Martynova, O.I.; Samojlov, Yu.F.; Petrova, T.I.; Kharitonova, N.L.

1983-01-01

Technique for calculation of solubility of iron corrosion products in oxygen-containing aqueous solutions in the 298-573 K temperature range is presented. Solubility of corrosion products of plain steel in deeply-desalinizated water in the presence of oxygen for the such range of the temperatures is experimentally determined. Rather good convergence between calculated and experimental data is noted

Drying characteristics of thorium fuel corrosion products

Energy Technology Data Exchange (ETDEWEB)

Smith, R.-E. E-mail: rzl@inel.gov

2004-07-01

The open literature and accessible US Department of Energy-sponsored reports were reviewed for the dehydration and rehydration characteristics of potential corrosion products from thorium metal and thorium oxide nuclear fuels. Mixed oxides were not specifically examined unless data were given for performance of mixed thorium-uranium fuels. Thorium metal generally corrodes to thorium oxide. Physisorbed water is readily removed by heating to approximately 200 deg. C. Complete removal of chemisorbed water requires heating above 1000 deg. C. Thorium oxide adsorbs water well in excess of the amount needed to cover the oxide surface by chemisorption. The adsorption of water appears to be a surface phenomenon; it does not lead to bulk conversion of the solid oxide to the hydroxide. Adsorptive capacity depends on both the specific surface area and the porosity of the thorium oxide. Heat treatment by calcination or sintering reduces the adsorption capacity substantially from the thorium oxide produced by metal corrosion.

Impact of β- radiolysis and transient products on irradiation-enhanced corrosion of zirconium alloys

International Nuclear Information System (INIS)

Lemaignan, C.

1992-01-01

An analysis has been undertaken of the various cases of local enhancement of the corrosion rate of zirconium alloys under irradiation. It is observed that in most cases a strong emission of energetic β - is present leading to a local energy desorption rate higher than the core average. This suggests that the local transient radiolytic oxidising species produced in the coolant by the β - particles could contribute to corrosion enhancement, by increasing the local corrosion potential. This process is applicable to the local enhanced corrosion found in front of stainless steels structural parts, due to the contribution of Mn, in front of Pt inserts and Cu-rich cruds. It explains also the irradiation corrosion enhancement of Cu-rich Zr alloys. Enhanced corrosion around neutron absorbing material is explained similarly by pair production from conversion of high energy capture photons in the cladding, leading to energetic electrons. The same process was found to be active with other highly ionising species like α in Ni-rich alloys and fission products in homogeneous reactors. This mechanism, applicable for an explanation of localised irradiation-enhanced corrosion, is proposed to be extended to the reactor core, where the general enhancement of Zr-alloy corrosion under irradiation would be due to the general radiolysis. It suggests that care should be taken to avoid any source of β - emission or other ionising species in the reactor core that could give an increase of energy deposition rate for radiolysis. Also the corrosion testing conditions for the materials to be used in reactors have to be relevant to the radiolytic environments found in the reactor cores. (orig.)

Oxidation kinetics of hydride-bearing uranium metal corrosion products

International Nuclear Information System (INIS)

Totemeier, T.C.; Pahl, R.G.; Frank, S.M.

1998-01-01

The oxidation behavior of hydride-bearing uranium metal corrosion products from zero power physics reactor (ZPPR) fuel plates was studied using thermo-gravimetric analysis (TGA) in environments of Ar-4%O 2 , Ar-9%O 2 , and Ar-20%O 2 . Ignition of corrosion product samples from two moderately corroded plates was observed between 125 C and 150 C in all environments. The rate of oxidation above the ignition temperature was found to be dependent only on the net flow rate of oxygen in the reacting gas. Due to the higher net oxygen flow rate, burning rates increased with increasing oxygen concentration. Oxidation rates below the ignition temperature were much slower and decreased with increasing test time. The hydride contents of the TGA samples from the two moderately corroded plates, determined from the total weight gain achieved during burning, were 47-61 wt% and 29-39 wt%. Samples from a lightly corroded plate were not reactive; X-ray diffraction (XRD) confirmed that they contained little hydride. (orig.)

Spectroscopic study of the final protective corrosion product on weathering steel

International Nuclear Information System (INIS)

Yamashita, M.; Misawa, T.

1998-01-01

Recent progress in understanding the structure and properties of final protective rust layer on weathering steel and its application for structural steels is shown based on the data obtained mainly by spectroscopic characterization. The main constituent of the weathering steel rust layer is changed with exposure period from γ- FeOOH (less than a few years) via, amorphous substance (several years), to α-FeOOH goethite phase (decades). The corrosion rate of the weathering steel decreased with this phase transformation. The final protective rust layer possesses the structure of α- (Fe 1 - X p Cr x)O OH, Cr substitute goethite; the crystal size decreases with its Cr-content. It is shown that the Cr content in the Cr-substituted goethite increases gradiently with reaching the rust/steel interface. This increase in the Cr content and resultant aggregation of fine crystals lead a densely packed Cr-substituted goethite rust layers which provides higher protective ability for atmospheric corrosives. It is found that the Cr-substituted goethite possesses the cation selective ability at the vicinity of the rust/steel interface where the Cr content can be estimated approximately 5-10 mass %. Thus, the final protective rust layer of the Cr-substituted goethite impedes the penetration of aggressive corrosive anions such as Cl - and SO 4 2- , besides the physically prevention effect of its densely aggregated structure for corrosive penetration. It is found that Cr 2 (SO 4 ) 3 is effective for obtaining the final protective rust layer in a short period. SO 4 2 accelerates rust formation and Cr 3- substitutes goethite crystal lattice point at the initial stage of corrosion; resultantly the rust layer formed suppresses dissolution of the steel even in the severe environment. (Author)

Deposition and incorporation of corrosion product to primary coolant suppressing method

International Nuclear Information System (INIS)

Tsuzuki, Yasuo; Hasegawa, Naoyoshi; Fujioka, Tsunaaki.

1992-01-01

In a PWR type nuclear power plant, the concentration of dissolved nitrogen in primary coolants is increased by controlling the nitrogen partial pressure in a volume controlling tank gas phase portion or addition of water in a primary system water supply tank containing dissolved nitrogen to a primary system. Then ammonium is formed by a reaction with hydrogen dissolved in the primary coolants in the field of radiation rays, to control the concentration of ammonium in the coolants within a range from 0.5 to 3.5 ppm, and operate the power plant. As a result, deposition and incorporation of corrosion products to the structural materials of the primary system equipments during plant operation (pH 6.8 to 8.0) are suppressed. In other words, deposition of particulate corrosion products on the surface of fuel cladding tubes and the inner surface of pipelines in the primary system main equipments is prevented and incorporation of ionic radioactive corrosion products to the oxide membranes on the inner surface of the pipelines of the primary system main equipments is suppressed, to greatly reduce the radiation dose rate of the primary system pipelines. Thus, operator's radiation exposure can be decreased upon shut down of the plant. (N.H.)

Corrosion product layers on magnesium alloys AZ31 and AZ61: Surface chemistry and protective ability

Science.gov (United States)

Feliu, S.; Llorente, I.

2015-08-01

This paper studies the chemical composition of the corrosion product layers formed on magnesium alloys AZ31 and AZ61 following immersion in 0.6 M NaCl, with a view to better understanding their protective action. Relative differences in the chemical nature of the layers were quantified by X-ray photoelectron spectroscopy (XPS), scanning electron microscopy (SEM), energy dispersive analysis of X-ray (EDX) and low-angle X-ray diffraction (XRD). Corrosion behavior was investigated by Electrochemical Impedance Spectroscopy (EIS) and hydrogen evolution measurement. An inhibitive effect from the corrosion product layers was observed from EIS, principally in the case of AZ31, as confirmed by hydrogen evolution tests. A link was found between carbonate enrichment observed by XPS in the surface of the corrosion product layer, concomitant with the increase in the protective properties observed by EIS.

Localized corrosion of high performance metal alloys in an acid/salt environment

Science.gov (United States)

Macdowell, L. G.; Ontiveros, C.

1991-01-01

Various vacuum jacketed cryogenic supply lines at the Space Shuttle launch site at Kennedy Space Center use convoluted flexible expansion joints. The atmosphere at the launch site has a very high salt content, and during a launch, fuel combustion products include hydrochloric acid. This extremely corrosive environment has caused pitting corrosion failure in the thin walled 304L stainless steel flex hoses. A search was done to find a more corrosion resistant replacement material. The study focussed on 19 metal alloys. Tests which were performed include electrochemical corrosion testing, accelerated corrosion testing in a salt fog chamber, and long term exposure at a beach corrosion testing site. Based on the results of these tests, several nickel based alloys were found to have very high resistance to this corrosive environment. Also, there was excellent agreement between the electrochemical tests and the actual beach exposure tests. This suggests that electrochemical testing may be useful for narrowing the field of potential candidate alloys before subjecting samples to long term beach exposure.

Electrochemical corrosion studies on a selected carbon steel for application in nuclear waste disposal containers: Influence of radiolytic products on corrosion in brines

International Nuclear Information System (INIS)

Farvaque-Bera, A.M.; Smailos, E.

1994-07-01

In previous corrosion studies, carbon steels were identified as promising materials for the manufacturing of long-lived high-level waste containers that could act as a radionuclide barrier in a rock-salt repository. In the present work, the influence of some important oxidizing radiolytic products generated in gamma irradiated brines on the electrochemical corrosion behaviour of the preselected fine-grained steel TStE 355 was studied. The steel was examined by potentiodynamic and potentiostatic polarization methods at 90 C in a disposal relevant NaCl-rich brine containing radiolytic products such as H 2 O 2 , ClO - , ClO 3 - and ClO 4 - at concentrations between 10 -4 and 10 -2 M/l. The significance of the radiolytic products to steel corrosion depends on their concentration at the metal-brine interface, which in turn, depends on many factors such as the dose rate, the amount of water present in the disposal area, the escape of gases (e.g. H 2 )

The atmospheric corrosion: an important technical-economic and nuclear safety factor during storage in the construction of nuclear power plants

International Nuclear Information System (INIS)

Rodriguez, R.; Rodriguez, J.; Diaz, J.; Gomez, J.; Galeano, N.

1993-01-01

The purpose of this work is to show the results of the research performed to determine the atmospheric corrosion in the region of Juragua nuclear power plant and to offer some practical recommendations to increase the efficiency during the storage of materials, considering technical-economic and nuclear safety aspects

Underground pipeline corrosion

CERN Document Server

Orazem, Mark

2014-01-01

Underground pipelines transporting liquid petroleum products and natural gas are critical components of civil infrastructure, making corrosion prevention an essential part of asset-protection strategy. Underground Pipeline Corrosion provides a basic understanding of the problems associated with corrosion detection and mitigation, and of the state of the art in corrosion prevention. The topics covered in part one include: basic principles for corrosion in underground pipelines, AC-induced corrosion of underground pipelines, significance of corrosion in onshore oil and gas pipelines, n

Modeling of Corrosion-induced Concrete Damage

DEFF Research Database (Denmark)

Thybo, Anna Emilie A.; Michel, Alexander; Stang, Henrik

2013-01-01

In the present paper a finite element model is introduced to simulate corrosion-induced damage in concrete. The model takes into account the penetration of corrosion products into the concrete as well as non-uniform formation of corrosion products around the reinforcement. To ac-count for the non...... of corrosion products affects both the time-to cover cracking and the crack width at the concrete surface.......In the present paper a finite element model is introduced to simulate corrosion-induced damage in concrete. The model takes into account the penetration of corrosion products into the concrete as well as non-uniform formation of corrosion products around the reinforcement. To ac-count for the non......-uniform formation of corrosion products at the concrete/reinforcement interface, a deterministic approach is used. The model gives good estimates of both deformations in the con-crete/reinforcement interface and crack width when compared to experimental data. Further, it is shown that non-uniform deposition...

75 FR 18153 - Corrosion-Resistant Carbon Steel Flat Products from the Republic of Korea: Extension of Time...

Science.gov (United States)

2010-04-09

... DEPARTMENT OF COMMERCE International Trade Administration [C-580-818] Corrosion-Resistant Carbon Steel Flat Products from the Republic of Korea: Extension of Time Limit for Preliminary Results of... countervailing duty order on corrosion-resistant carbon steel flat products (CORE) from Korea. See Countervailing...

77 FR 16810 - Corrosion-Resistant Carbon Steel Flat Products From the Republic of Korea: Extension of Time...

Science.gov (United States)

2012-03-22

... DEPARTMENT OF COMMERCE International Trade Administration [C-580-818] Corrosion-Resistant Carbon Steel Flat Products From the Republic of Korea: Extension of Time Limit for Preliminary Results of... Register the countervailing duty order on corrosion-resistant carbon steel flat products (CORE) from Korea...

76 FR 20954 - Corrosion-Resistant Carbon Steel Flat Products From the Republic of Korea: Extension of Time...

Science.gov (United States)

2011-04-14

... DEPARTMENT OF COMMERCE International Trade Administration [C-580-818] Corrosion-Resistant Carbon Steel Flat Products From the Republic of Korea: Extension of Time Limit for Preliminary Results of... Register the countervailing duty order on corrosion-resistant carbon steel flat products (CORE) from Korea...

Analysis of corrosion-product transport using nondestructive XRF and MS techniques

International Nuclear Information System (INIS)

Sawicka, B.D.; Sawicki, J.A.

1998-01-01

This paper describes the application of X-ray fluorescence (XRF) and Moessbauer spectroscopy (MS) techniques to monitor corrosion-product transport (CPT) in water circuits of nuclear reactors. The combination of XRF and MS techniques was applied in studies of CPT crud filters from both primary- and secondary-side water circuits (i.e., radioactive and nonradioactive specimens) of CANDU reactors. The XRF-MS method allows nondestructive analysis of species collected on filters and provides more complete information about corrosion products than commonly used digestive methods of chemical analysis. Recent analyses of CPT specimens from the Darlington Nuclear Generating Station (NGS) primary side and the Bruce B NGS feedwater system are shown as examples. Some characteristics of primary and secondary water circuits are discussed using these new data. (author)

Simulation of corrosion product activity in pressurized water reactors under flow rate transients

International Nuclear Information System (INIS)

Mirza, Anwar M.; Mirza, Nasir M.; Mir, Imran

1998-01-01

Simulation of coolant activation due to corrosion products and impurities in a typical pressurized water reactor has been done under flow rate transients. Employing time dependent production and losses of corrosion products in the primary coolant path an approach has been developed to calculate the coolant specific activity. Results for 24 Na, 56 Mn, 59 Fe, 60 Co and 99Mo show that the specific activity in primary loop approaches equilibrium value under normal operating conditions fairly rapidly. Predominant corrosion product activity is due to Mn-56. Parametric studies at full power for various ramp decreases in flow rate show initial decline in the activity and then a gradual rise to relatively higher saturation values. The minimum value and the time taken to reach the minima are strong functions of the slope of linear decrease in flow rate. In the second part flow rate coastdown was allowed to occur at different flow half-times. The reactor scram was initiated at 90% of the normal flow rate. The results show that the specific activity decreases and the rate of decrease depends on pump half time and the reactor scram conditions

77 FR 25405 - Corrosion-Resistant Carbon Steel Flat Products From the Republic of Korea: Extension of Time...

Science.gov (United States)

2012-04-30

... antidumping duty order on corrosion-resistant carbon steel flat products from the Republic of Korea, covering... DEPARTMENT OF COMMERCE International Trade Administration [A-580-816] Corrosion-Resistant Carbon Steel Flat Products From the Republic of Korea: Extension of Time Limit for the Preliminary Results of...

76 FR 21332 - Corrosion-Resistant Carbon Steel Flat Products From the Republic of Korea: Extension of Time...

Science.gov (United States)

2011-04-15

... antidumping duty order on corrosion-resistant carbon steel flat products from the Republic of Korea, covering... DEPARTMENT OF COMMERCE International Trade Administration [A-580-816] Corrosion-Resistant Carbon Steel Flat Products From the Republic of Korea: Extension of Time Limits for the Preliminary Results of...

75 FR 25841 - Corrosion-Resistant Carbon Steel Flat Products From the Republic of Korea: Extension of Time...

Science.gov (United States)

2010-05-10

... antidumping duty order on corrosion-resistant carbon steel flat products from the Republic of Korea, covering... DEPARTMENT OF COMMERCE International Trade Administration [A-580-816] Corrosion-Resistant Carbon Steel Flat Products From the Republic of Korea: Extension of Time Limits for the Preliminary Results of...

Corrosion in the oil industry

Energy Technology Data Exchange (ETDEWEB)

Brondel, D [Sedco Forex, Montrouge (France); Edwards, R [Schlumberger Well Services, Columbus, OH (United States); Hayman, A [Etudes et Productions Schlumberger, Clamart (France); Hill, D [Schlumberger Dowell, Tulsa, OK (United States); Mehta, S [Schlumberger Dowell, St. Austell (United Kingdom); Semerad, T [Mobil Oil Indonesia, Inc., Sumatra (Indonesia)

1994-04-01

Corrosion costs the oil industry billions of dollars a year, a fact that makes the role of the corrosion engineer an increasingly important one. Attention is paid to how corrosion affects every aspect of exploration and production, from offshore rigs to casing. Also the role of corrosion agents such as drilling and production fluids is reviewed. Methods of control and techniques to monitor corrosion are discussed, along with an explanation of the chemical causes of corrosion. 21 figs., 32 refs.

Construction and Application of a National Data-Sharing Service Network of Material Environmental Corrosion

Directory of Open Access Journals (Sweden)

Xiaogang Li

2007-12-01

Full Text Available This article discusses the key features of a newly developed national data-sharing online network for material environmental corrosion. Written in Java language and based on Oracle database technology, the central database in the network is supported with two unique series of corrosion failure data, both of which were accumulated during a long period of time. The first category of data, provided by national environment corrosion test sites, is corrosion failure data for different materials in typical environments (atmosphere, seawater and soil. The other category is corrosion data in production environments, provided by a variety of firms. This network system enables standardized management of environmental corrosion data, an effective data sharing process, and research and development support for new products and after-sale services. Moreover this network system provides a firm base and data-service platform for the evaluation of project bids, safety, and service life. This article also discusses issues including data quality management and evaluation in the material corrosion data sharing process, access authority of different users, compensation for providers of shared historical data, and finally, the related policy and law legal processes, which are required to protect the intellectual property rights of the database.

Strontium concentrations in corrosion products from residential drinking water distribution systems.

Science.gov (United States)

Gerke, Tammie L; Little, Brenda J; Luxton, Todd P; Scheckel, Kirk G; Maynard, J Barry

2013-05-21

The United States Environmental Protection Agency (US EPA) will require some U.S. drinking water distribution systems (DWDS) to monitor nonradioactive strontium (Sr(2+)) in drinking water in 2013. Iron corrosion products from four DWDS were examined to assess the potential for Sr(2+) binding and release. Average Sr(2+) concentrations in the outermost layer of the corrosion products ranged from 3 to 54 mg kg(-1) and the Sr(2+) drinking water concentrations were all ≤0.3 mg L(-1). Micro-X-ray adsorption near edge structure spectroscopy and linear combination fitting determined that Sr(2+) was principally associated with CaCO3. Sr(2+) was also detected as a surface complex associated with α-FeOOH. Iron particulates deposited on a filter inside a home had an average Sr(2+) concentration of 40.3 mg kg(-1) and the associated drinking water at a tap was 210 μg L(-1). The data suggest that elevated Sr(2+) concentrations may be associated with iron corrosion products that, if disturbed, could increase Sr(2+) concentrations above the 0.3 μg L(-1) US EPA reporting threshold. Disassociation of very small particulates could result in drinking water Sr(2+) concentrations that exceed the US EPA health reference limit (4.20 mg kg(-1) body weight).

Oxidation kinetics of hydride-bearing uranium metal corrosion products

Science.gov (United States)

Totemeier, Terry C.; Pahl, Robert G.; Frank, Steven M.

The oxidation behavior of hydride-bearing uranium metal corrosion products from Zero Power Physics Reactor (ZPPR) fuel plates was studied using thermo-gravimetric analysis (TGA) in environments of Ar-4%O 2, Ar-9%O 2, and Ar-20%O 2. Ignition of corrosion product samples from two moderately corroded plates was observed between 125°C and 150°C in all environments. The rate of oxidation above the ignition temperature was found to be dependent only on the net flow rate of oxygen in the reacting gas. Due to the higher net oxygen flow rate, burning rates increased with increasing oxygen concentration. Oxidation rates below the ignition temperature were much slower and decreased with increasing test time. The hydride contents of the TGA samples from the two moderately corroded plates, determined from the total weight gain achieved during burning, were 47-61 wt% and 29-39 wt%. Samples from a lightly corroded plate were not reactive; X-ray diffraction (XRD) confirmed that they contained little hydride.

Corrosion behaviour of Mg/Al alloys in high humidity atmospheres

Energy Technology Data Exchange (ETDEWEB)

Arrabal, R.; Pardo, A.; Merino, M.C.; Mohedano, M.; Casajus, P. [Facultad de Quimicas, Departamento de Ciencia de Materiales, Universidad Complutense, 28040 Madrid (Spain); Merino, S. [Departamento de Tecnologia Industrial, Universidad Alfonso X El Sabio, Villanueva de la Canada, 28691 Madrid (Spain)

2011-04-15

The influence of relative humidity (80-90-98% RH) and temperature (25 and 50 C) on the corrosion behaviour of AZ31, AZ80 and AZ91D magnesium alloys was evaluated using gravimetric measurements. The results were compared with the data obtained for the same alloys immersed in Madrid tap water. The corrosion rates of AZ alloys increased with the RH and temperature and were influenced by the aluminium content and alloy microstructure for RH values above 90%. The initiation of corrosion was localised around the Al-Mn inclusions in the AZ31 alloy and at the centre of the {alpha}-Mg phase in the AZ80 and AZ91D alloys. The {beta}-Mg{sub 17}Al{sub 12} phase acted as a barrier against corrosion. (Copyright copyright 2011 WILEY-VCH Verlag GmbH and Co. KGaA, Weinheim)

Microbially influenced corrosion of zinc and aluminium - Two-year subjection to influence of Aspergillus niger

Energy Technology Data Exchange (ETDEWEB)

Juzeliunas, Eimutis [Institute of Chemistry, A.Gostauto 9, 01108 Vilnius (Lithuania)], E-mail: ejuzel@ktl.mii.lt; Ramanauskas, Rimantas; Lugauskas, Albinas; Leinartas, Konstantinas; Samuleviciene, Meilute; Sudavicius, Aloyzas; Juskenas, Remigijus [Institute of Chemistry, A.Gostauto 9, 01108 Vilnius (Lithuania)

2007-11-15

Aspergillus niger. Tiegh., a filamentous ascomycete fungus, was isolated from the metal samples exposed to marine, rural and urban sites in Lithuania. Al and Zn samples were subjected to two-year influence of A. niger under laboratory conditions in humid atmosphere. Electrochemical impedance spectroscopy (EIS) ascertained microbially influenced corrosion acceleration (MICA) of Zn and inhibition (MICI) of Al. EIS data indicated a two-layer structure of corrosion products on Zn. The microorganisms reduced the thickness of the inner layer, whose passivating capacity was much higher when compared to that of the outer layer. An increase in aluminium oxide layer resistance but decrease in the layer thickness implied that MICI affected primarily the sites of localized corrosion of Al (pores, micro-cracks, etc.). X-ray diffraction (XRD) and X-ray photoelectron spectroscopy (XPS) studies indicated that bioproducts (i.e. organic acids) did not form crystalline phases with corrosion products of zinc. The study suggested a hypothesis that microorganisms could be used as corrosion protectors instead of toxic chemicals, application of which tends to be increasingly restricted.

Microbially influenced corrosion of zinc and aluminium - Two-year subjection to influence of Aspergillus niger

International Nuclear Information System (INIS)

Juzeliunas, Eimutis; Ramanauskas, Rimantas; Lugauskas, Albinas; Leinartas, Konstantinas; Samuleviciene, Meilute; Sudavicius, Aloyzas; Juskenas, Remigijus

2007-01-01

Aspergillus niger. Tiegh., a filamentous ascomycete fungus, was isolated from the metal samples exposed to marine, rural and urban sites in Lithuania. Al and Zn samples were subjected to two-year influence of A. niger under laboratory conditions in humid atmosphere. Electrochemical impedance spectroscopy (EIS) ascertained microbially influenced corrosion acceleration (MICA) of Zn and inhibition (MICI) of Al. EIS data indicated a two-layer structure of corrosion products on Zn. The microorganisms reduced the thickness of the inner layer, whose passivating capacity was much higher when compared to that of the outer layer. An increase in aluminium oxide layer resistance but decrease in the layer thickness implied that MICI affected primarily the sites of localized corrosion of Al (pores, micro-cracks, etc.). X-ray diffraction (XRD) and X-ray photoelectron spectroscopy (XPS) studies indicated that bioproducts (i.e. organic acids) did not form crystalline phases with corrosion products of zinc. The study suggested a hypothesis that microorganisms could be used as corrosion protectors instead of toxic chemicals, application of which tends to be increasingly restricted

Durability of bare and anodised aluminium in atmosphere of very different corrosivities I. Bare aluminium; Durabilidad del aluminio desnudo y anodizado en atmosferas de muy diferentes corrosividades. I. Aluminio desnudo

Energy Technology Data Exchange (ETDEWEB)

Gonzalez, J. A.; Escudero, E.; Lopez, V.; Simancas, J.; Morcillo, M.

2004-07-01

The behaviour of bare aluminium is studied in atmospheric exposure at 11 natural testing stations with salinity levels ranging between 2.1 and 684 mg Cl''- m''-2 d''-1. In atmospheres of low or moderate aggressivity aluminium behaves as a passive material, though the insignificant corrosion that is produced is sufficient to spoil its appearance. In contrast, at salinity levels of 50 mg Cl''- m''-2 ''-1 or above, aluminium is susceptible to pitting corrosion even in the first year of atmospheric exposure, or in the second year at salinities of {<=} 10 mg Cl''- m''-2 d''-1. For comparative purposes, results are included for aluminium protected with an anodic film of 28 {mu}m thickness exposed at the same testing stations. A 28 {mu}m anodic film, correctly sealed, prevents the risk of localised corrosion even in the most unfavourable situations. (Author) 23 refs.

Mass transfer of corrosion products in high temperature, high pressure water circuits

International Nuclear Information System (INIS)

Rodd, J.T.; Nicholson, F.D.

1976-01-01

The CWL-3 loop is used to study the mass transfer of corrosion products in water at 270 0 C for pressures up to 6.9 MPa. Two parallel Zircaloy-2 test sections are heated directly by a low voltage a.c. electrical current to give a heat flux up to 500 W cm -2 and a heat rating up to 1500 W cm -1 . Coolant flow rates can be varied up to 0.4 kg cm -2 s -1 with or without boiling. A tracer technique has been developed to monitor continuously the deposition of corrosion products in the test sections during operation of the loop. Magnetite deposits 2.6 nm thick can be readily detected. (author)

Standard Practice for Recording Data from Atmospheric Corrosion Tests of Metallic-Coated Steel Specimens

CERN Document Server

American Society for Testing and Materials. Philadelphia

2010-01-01

1.1 This practice covers a procedure for recording data of atmospheric corrosion tests of metallic-coated steel specimens. Its objective is the assurance of (1) complete identification of materials before testing, (2) objective reporting of material appearance during visual inspections, and (3) adequate photographic, micrographic, and chemical laboratory examinations at specific stages of deterioration, and at the end of the tests. 1.2 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety and health practices and determine the applicability of regulatory limitations prior to use.

Corrosion evaluation technology

International Nuclear Information System (INIS)

Kim, Uh Chul; Han, Jeong Ho; Nho, Kye Ho; Lee, Eun Hee; Kim, Hong Pyo; Hwang, Seong Sik; Lee, Deok Hyun; Hur, Do Haeng; Kim, Kyung Mo.

1997-09-01

A multifrequency ACPD system was assembled which can measure very small crack. Stress corrosion cracking test system with SSRT operating high temperature was installed. Stress corrosion cracking test of newly developed alloy 600 and existing alloy 600 was carried out in steam atmosphere of 400 deg C. No crack was observed in both materials within a test period of 2,000 hrs. Corrosion fatigue test system operating at high temperature was installed in which fatigue crack was measured by CDPD. Lead enhanced the SCC of the Alloy 600 in high temperature water, had a tendency to modify a cracking morphology from intergranular to transgranular. Pit initiation preferentially occurred at Ti-rich carbide. Resistance to pit initiation decreased with increasing temperature up to 300 deg C. Test loop for erosion corrosion was designed and fabricated. Thin layer activation technique was very effective in measuring erosion corrosion. Erosion corrosion of a part of secondary side pipe was evaluated by the Check Family Codes of EPRI. Calculated values of pipe thickness by Check Family Codes coincided with the pipe thickness measured by UT with an error of ± 20%. Literature review on turbine failure showed that failure usually occurred in low pressure turbine rotor disc and causes of failure are stress corrosion cracking and corrosion fatigue. (author). 12 refs., 20 tabs., 77 figs

Catalysis of copper corrosion products on chlorine decay and HAA formation in simulated distribution systems.

Science.gov (United States)

Zhang, Hong; Andrews, Susan A

2012-05-15

This study investigated the effect of copper corrosion products, including Cu(II), Cu(2)O, CuO and Cu(2)(OH)(2)CO(3), on chlorine degradation, HAA formation, and HAA speciation under controlled experimental conditions. Chlorine decay and HAA formation were significantly enhanced in the presence of copper with the extent of copper catalysis being affected by the solution pH and the concentration of copper corrosion products. Accelerated chlorine decay and increased HAA formation were observed at pH 8.6 in the presence of 1.0 mg/L Cu(II) compared with that observed at pH 6.6 and pH 7.6. Further investigation of chlorine decay in the presence of both Suwannee River NOM and Cu(II) indicated that an increased reactivity of NOM with dissolved and/or solid surface-associated Cu(II), rather than chlorine auto-decomposition, was a primary reason for the observed rapid chlorine decay. Copper corrosion solids [Cu(2)O, CuO, Cu(2)(OH)(2)CO(3)] exhibited catalytic effects on both chlorine decay and HAA formation. Contrary to the results observed when in the absence of copper corrosion products, DCAA formation was consistently predominant over other HAA species in the presence of copper corrosion products, especially at neutral and high pH. This study improves the understanding for water utilities and households regarding chlorine residuals and HAA concentrations in distribution systems, in particular once the water reaches domestic plumbing where copper is widely used. Copyright © 2012 Elsevier Ltd. All rights reserved.

Radioactive corrosion products in circuit of fast reactor loop with dissociating coolant

International Nuclear Information System (INIS)

Dolgov, V.M.; Katanaev, A.O.

1982-01-01

The results of experimental investigation into depositions of radionuclides of corrosion origin on the surfaces of a reactor-in-pile loop facility with a dissociating coolant are presented. It is stated that the ratio of radionuclides in fixed depositions linearly decreases with decrease of the coolant temperature at the core-condenser section. The element composition of non-fixed compositions quantitatively and qualitatively differs from the composition of structural material, and it is more vividly displayed for the core-condenser section. The main mechanism of circuit contamination with radioactive corrosion products is substantiated: material corrosion in the zones of coolant phase transfer, their remove by the coolant in the core, deposition, activation and wash-out by the coolant from the core surfaces

Influence of stainless steel Internals on Corrosion of tower wall materials

Science.gov (United States)

Chen, Bing; Ren, Ke

2017-12-01

In view of the galvanic corrosion of the tower wall material in the tower of a refinery atmospheric vacuum distillation unit, the electrochemical behavior of Q345R steel, stainless steel (201, 304 cold-rolled plate, 304 hot rolled plate and 316L) in 3.5%NaCl solution was studied by electrochemical method. The results show that the corrosion potential of Q345R is much lower than that of stainless steel, and the corrosion rate of Q345R is higher than that of stainless steel. As the anode is etched as the anode corrosion, the anode polarizability of stainless steel shows strong polarization ability, which is anodic polarization control, and Q345R is anode Active polarization control; Q345R / 201 galvanic pair may be the most serious corrosion, and Q345R/316L galvanic couple may be relatively slight. Therefore, in the actual production of tower equipment, material design or tower to upgrade the replacement, it are recommended to use the preferred anode and cathode potential difference with the use of materials.

Synergy effect of naphthenic acid corrosion and sulfur corrosion in crude oil distillation unit

Science.gov (United States)

Huang, B. S.; Yin, W. F.; Sang, D. H.; Jiang, Z. Y.

2012-10-01

The synergy effect of naphthenic acid corrosion and sulfur corrosion at high temperature in crude oil distillation unit was studied using Q235 carbon-manganese steel and 316 stainless steel. The corrosion of Q235 and 316 in corrosion media containing sulfur and/or naphthenic acid at 280 °C was investigated by weight loss, scanning electron microscope (SEM), EDS and X-ray diffractometer (XRD) analysis. The results showed that in corrosion media containing only sulfur, the corrosion rate of Q235 and 316 first increased and then decreased with the increase of sulfur content. In corrosion media containing naphthenic acid and sulfur, with the variations of acid value or sulfur content, the synergy effect of naphthenic acid corrosion and sulfur corrosion has a great influence on the corrosion rate of Q235 and 316. It was indicated that the sulfur accelerated naphthenic acid corrosion below a certain sulfur content but prevented naphthenic acid corrosion above that. The corrosion products on two steels after exposure to corrosion media were investigated. The stable Cr5S8 phases detected in the corrosion products film of 316 were considered as the reason why 316 has greater corrosion resistance to that of Q235.

Iron Drinking Water Pipe Corrosion Products: Concentrators of Toxic Metals

Science.gov (United States)

2013-01-01

health risk. In addition Pb corrosion products may be sinks for other metals such as chromium (Cr), copper (Cu), manganese (Mn), and zinc (Zn). These...Vanadium K-Edge X-ray Absorption Near-Edge Structure Interpretation: Application to the Speciation of Vanadium in Oxide Phases from Steel Slag ’, Journal

Corrosion Product Measurements to ensure integrity of the Steam Generators in Beznau NPP

International Nuclear Information System (INIS)

Mailand, Irene; Franz, Patrick; Venz, Hartmut

2012-09-01

The Nuclear Power Plant Beznau comprises two identical 380 MWe PWR units with two loops each, commissioned in 1969 and 1971. Westinghouse was responsible for the primary part of the plant and BBC/ABB for the secondary circuit. The original materials used in the secondary systems were made of several copper-based alloys, such as for the Condensers, the Low Pressure Pre-heaters and the Moisture Separator Re-heater. The original Steam Generator Tubes were made of Inconel 600 MA. Regarding its age, the NPP Beznau has to be qualified as an old plant. However, in fact particularly in the last 20 years the plant has undergone an extensive modernisation programme in which about 1.5 billion Swiss Francs have been invested. Important measures were the replacements of the Steam Generators with tubes comprising Inconel 690 TT which was realized at unit 1 in 1993 and at unit 2 in 1999. Copper was completely banished from the secondary system and replaced by stainless and chromium steel. The Condensers were fitted with titanium tubes. The secondary water chemistry had to be changed by these replacements and moved step by step from Low-AVT with a pH of about 9.3 to High-AVT with a pH of 9.8 to 9.9, currently. To ensure the integrity of the new Steam Generators as well as of the whole Secondary System a corrosion product programme was introduced at the end of the Nineties. Several investigations which are performed periodically are represented by analyses of corrosion products, measurements of sludge mass and composition in the Steam Generators, Hide-Out-Return- and mass balance measurements of corrosion products in the whole circuit. Objectives of these investigations are assessments of the efficiency of the water chemistry and trend considerations regarding to the transport of corrosion products and pollutants into the Steam Generator, as well as of the potential danger of deposits and stored or absorbed pollutants. The main target of all measures is to avoid any chemical

Effect of boron control of environment on corrosion and resistance to low-cycle corrosion fatigue in structural steels

International Nuclear Information System (INIS)

Babej, Yu.I.; Zhitkov, V.V.; Zvezdin, Yu.I.; Liskevich, I.Yu.; Nazarov, A.A.

1982-01-01

Tests of the specimens on total, contact and crevice corrosion, corrosion cracking and low-cycle fatigue are conducted for determination of corrosion and corrosion-fatigue characteristics in the 15Kh3NMFA, 10N3MFA, 10Kh16N4B, 05Kh13N6M2 structural steels, used in energetics. The environment is subjected to boron control and contacting with atmosphere for simulation of stop and operation modes of the facility. The experiments are carried out in the distilled water with 12g/l H 3 BO 3 and 10 mg/l Cl' at 25, 60, 100 deg C under contacting with atmosphere. It is established, that the pearlitic steels 15Kh3NMFA, 10N3MFA, as well as transition and martensitic 05Kh13N6M2 and 10Kh16N4B steels are highly stable to total, crevice and contact corrosion at the high parameters of aqueous boron-containing medium. Steel resistance to low-cycle fracture decreases slightly under the conditions similar to the operation ones, in the water with 12 g/l H 3 BO 3 . Durability of the pearlitic steels at the simulation of stop conditions decreases more noticeably, crack formation as a rule, initiating from corrosion spots

NASA's Corrosion Technology Laboratory at the Kennedy Space Center: Anticipating, Managing, and Preventing Corrosion

Science.gov (United States)

Calle, Luz Marina

2015-01-01

The marine environment at NASAs Kennedy Space Center (KSC) has been documented by ASM International (formerly American Society for Metals) as the most corrosive in North America. With the introduction of the Space Shuttle in 1981, the already highly corrosive conditions at the launch pads were rendered even more severe by the highly corrosive hydrochloric acid (HCl) generated by the solid rocket boosters (SRBs). Numerous failures at the launch pads are caused by corrosion. The structural integrity of ground infrastructure and flight hardware is critical to the success, safety, cost, and sustainability of space missions. NASA has over fifty years of experience dealing with unexpected failures caused by corrosion and has developed expertise in corrosion control in the launch and other environments. The Corrosion Technology Laboratory at KSC evolved, from what started as an atmospheric exposure test site near NASAs launch pads, into a capability that provides technical innovations and engineering services in all areas of corrosion for NASA, external partners, and customers.This paper provides a chronological overview of NASAs role in anticipating, managing, and preventing corrosion in highly corrosive environments. One important challenge in managing and preventing corrosion involves the detrimental impact on humans and the environment of what have been very effective corrosion control strategies. This challenge has motivated the development of new corrosion control technologies that are more effective and environmentally friendly. Strategies for improved corrosion protection and durability can have a huge impact on the economic sustainability of human spaceflight operations.

High temperature chlorosilane corrosion of iron and AISI 316L stainless steel

Science.gov (United States)

Aller, Joshua Loren

Chlorosilane gas streams are used at high temperatures (>500°C) throughout the semiconductor, polycrystalline silicon, and fumed silica industries, primarily as a way to refine, deposit, and produce silicon and silicon containing materials. The presence of both chlorine and silicon in chlorosilane species creates unique corrosion environments due to the ability of many metals to form both metal-chlorides and metal-silicides, and it is further complicated by the fact that many metal-chlorides are volatile at high-temperatures while metal-silicides are generally stable. To withstand the uniquely corrosive environments, expensive alloys are often utilized, which increases the cost of final products. This work focuses on the corrosion behavior of iron, the primary component of low-cost alloys, and AISI 316L, a common low-cost stainless steel, in environments representative of industrial processes. The experiments were conducted using a customized high temperature chlorosilane corrosion system that exposed samples to an atmospheric pressure, high temperature, chlorosilane environment with variable input amounts of hydrogen, silicon tetrachloride, and hydrogen chloride plus the option of embedding samples in silicon during the exposure. Pre and post exposure sample analysis including scanning electron microscopy, x-ray diffraction, energy dispersive x-ray spectroscopy, and gravimetric analysis showed the surface corrosion products varied depending on the time, temperature, and environment that the samples were exposed to. Most commonly, a volatile chloride product formed first, followed by a stratified metal silicide layer. The chlorine and silicon activities in the corrosion environment were changed independently and were found to significantly alter the corrosion behavior; a phenomenon supported by computational thermodynamic equilibrium simulations. It was found that in comparable environments, the stainless steel corroded significantly less than the pure iron. This

The Influence of Pseudomonas fluorescens on Corrosion Products of Archaeological Tin-Bronze Analogues

Science.gov (United States)

Ghiara, G.; Grande, C.; Ferrando, S.; Piccardo, P.

2018-01-01

In this study, tin-bronze analogues of archaeological objects were investigated in the presence of an aerobic Pseudomonas fluorescens strain in a solution, containing chlorides, sulfates, carbonates and nitrates according to a previous archaeological characterization. Classical fixation protocols were employed in order to verify the attachment capacity of such bacteria. In addition, classical metallurgical analytical techniques were used to detect the effect of bacteria on the formation of uncommon corrosion products in such an environment. Results indicate quite a good attachment capacity of the bacteria to the metallic surface and the formation of the uncommon corrosion products sulfates and sulfides is probably connected to the bacterial metabolism.

Chemical vapour deposition at atmospheric pressure of graphene on molybdenum foil: Effect of annealing time on characteristics and corrosion stability of graphene coatings

International Nuclear Information System (INIS)

Naghdi, Samira; Jevremović, Ivana; Mišković-Stanković, Vesna; Rhee, Kyong Yop

2016-01-01

Highlights: • Atmospheric pressure chemical vapor deposition of graphene on molybdenum foils. • Quality and domain size of graphene layers increased with longer annealing times. • The number of graphene layers decreased with longer annealing times. • Graphene coatings on molybdenum foils exhibited corrosion inhibitive properties. - Abstract: In this work, the effect of pre-annealing of Mo substrate on the quality of graphene layers grown by chemical vapour deposition was investigated by X-ray diffraction, X-ray photoelectron spectroscopy, and Raman spectroscopy. Moreover, different electrochemical techniques were employed to investigate the corrosion stability of the graphene coated Mo in 0.1 M NaCl. Longer annealing time resulted in less defective graphene coatings with fewer layers. Graphene coating on the annealed Mo provided better protection against corrosion during the initial exposure times, while after prolonged exposure times, both graphene coatings on annealed and non-annealed Mo exhibited nearly the same corrosion inhibitive properties.

Evaluation of atmospheric corrosion on electroplated zinc and zinc nickel coatings by Electrical Resistance (ER) Monitoring

DEFF Research Database (Denmark)

Møller, Per

2013-01-01

ER (Electrical Resistance) probes provide a measurement of metal loss, measured at any time when a metal is exposed to the real environment. The precise electrical resistance monitoring system can evaluate the corrosion to the level of nanometers, if the conductivity is compensated for temperature...... and magnetic fields. With this technique very important information about the durability of a new conversion coatings for aluminum, zinc and zinc alloys exposed to unknown atmospheric conditions can be gathered. This is expected to have a major impact on a number of industrial segments, such as test cars...

Evaluation of CRUDTRAN code to predict transport of corrosion products and radioactivity in the PWR primary coolant system

International Nuclear Information System (INIS)

Lee, C.B.

2002-01-01

CRUDTRAN code is to predict transport of the corrosion products and their radio-activated nuclides such as cobalt-58 and cobalt-60 in the PWR primary coolant system. In CRUDTRAN code the PWR primary circuit is divided into three principal sections such as the core, the coolant and the steam generator. The main driving force for corrosion product transport in the PWR primary coolant comes from coolant temperature change throughout the system and a subsequent change in corrosion product solubility. As the coolant temperature changes around the PWR primary circuit, saturation status of the corrosion products in the coolant also changes such that under-saturation in steam generator and super-saturation in the core. CRUDTRAN code was evaluated by comparison with the results of the in-reactor loop tests simulating the PWR primary coolant system and PWR plant data. It showed that CRUDTRAN could predict variations of cobalt-58 and cobalt-60 radioactivity with time, plant cycle and coolant chemistry in the PWR plant. (author)

76 FR 55004 - Certain Corrosion-Resistant Carbon Steel Flat Products From the Republic of Korea: Preliminary...

Science.gov (United States)

2011-09-06

... DEPARTMENT OF COMMERCE International Trade Administration [A-580-816] Certain Corrosion-Resistant...) is conducting the seventeenth administrative review of the antidumping order on corrosion-resistant carbon steel flat products (CORE) from the Republic of Korea \\1\\ (Korea). This review covers eight...

Effect of Rare Earth on Corrosion Products and Impedance Behavior of AZ91 Magnesium Alloy Under Dry-wet Cycles

Directory of Open Access Journals (Sweden)

ZHAO Xi

2017-04-01

Full Text Available The effect of mischmetal of lanthanum and cerium on the composition and structure of the corrosion products on the surface of AZ91 Mg alloy in deicing salt solution under dry-wet cycles was investigated by scanning electron microscopy (SEM, X-ray diffraction (XRD and energy dispersive spectrometer (EDS. The results show that the corrosion products of AZ91 Mg alloy without mischmetal addition (La,Ce are mainly composed of Mg(OH2, MgO, CaCO3 and Mg6Al2CO3(OH16·4H2O; and (La,CeAlO3 can be found in the products of AZ91 with mischmetal addition, meanwhile dense layer occurs in the corrosion products. Electrochemical impedance spectroscopy (EIS measurements show that the charge transfer resistance of AZ91 alloy with mischmetal addition tested in the same dry-wet cycles is much higher than that of AZ91 alloy, the addition of mischmetal helps to reduce the dispersing effect of impedance spectroscopy, indicating that the corrosion resistance of AZ91 Mg alloy and the stability of corrosion product films can be improved by mischmetal of La and Ce.

Task E container corrosion studies: Annual report

International Nuclear Information System (INIS)

Bunnell, L.R.; Doremus, L.A.; Topping, J.B.; Duncan, D.R.

1994-06-01

The Pacific Northwest Laboratory is conducting the Solid Waste Technology Support Program (SWTSP) for Westinghouse Hanford Company (WHC). Task E is the Container Corrosion Study Portion of the SWTSP that will perform testing to provide defensible data on the corrosion of low-carbon steel, as used in drums to contain chemical and radioactive wastes at the Hanford Site. A second objective of Task E is to provide and test practical alternative materials that have higher corrosion resistance than low-carbon steel. The scope of work for fiscal year (FY) 1993 included initial testing of mild steel specimens buried in Hanford soils or exposed to atmospheric corrosion in metal storage sheds. During FY 1993, progress was made in three areas of Task E. First, exposure of test materials began at the Soil Corrosion Test Site where low-carbon steel specimens were placed in the soil in five test shafts at depths of 9 m (30 ft). Second, the corrosion measurement of low-carbon steel in the soil of two solid waste trenches continued. The total exposure time is ∼ 500 days. Third, an atmospheric corrosion test of low-carbon steel was put initiated in a metal shed (Building 2401-W) in the 200 West Area. This annual report describes the Task E efforts and provides a current status

Study on metal material corrosion behavior of packaging of cement solidified form

International Nuclear Information System (INIS)

He Zhouguo; Lin Meiqiong; Fan Xianhua

1997-01-01

The corrosion behavior of A3 carbon steel is studied by the specimens that are exposed to atmosphere, embedded in cement solidified form or immersed in corrosion liquid. The corrosion rate is determined by mass change of the specimens. In order to compare the corrosion resistant performance of various coatings, the specimens painted with various material such as epoxide resin, propionic acid resin, propane ether resin and Ti-white paint are tested. The results of the tests show that corrosion rate of A3 carbon steel is less than 10 -3 mm·a -1 in the atmosphere and the cement solidified from, less than 0.1 mm·a -1 in the corrosion liquids, and pH value in the corrosion liquids also affect the corrosion rate of A3 carbon steel. The corrosion resistant performance of Ti-white paint is better than that of other paints. So, A3 carbon steel as packaging material can meet the requirements during storage

The Behavior of Environmentally Friendly Corrosion Preventative Compounds in an Aggressive Coastal Marine Environment

Science.gov (United States)

Montgomery, Eliza L.; Calle, Luz Marina; Curran Jerome C.; Kolody, Mark R.

2013-01-01

The shift to use environmentally friendly technologies throughout future space-related launch programs prompted a study aimed at replacing current petroleum and solvent-based Corrosion Preventive Compounds (CPCs) with environmentally friendly alternatives. The work in this paper focused on the identification and evaluation of environmentally friendly CPCs for use in protecting flight hardware and ground support equipment from atmospheric corrosion. The CPCs, while a temporary protective coating, must survive in the aggressive coastal marine environment that exists throughout the Kennedy Space Center, Florida. The different protection behaviors of fifteen different soft film CPCs, both common petroleum-based and newer environmentally friendly types, were evaluated on various steel and aluminum substrates. The CPC and substrate systems were subjected to atmospheric testing at the Kennedy Space Center's Beachside Atmospheric Corrosion Test Site, as well as cyclic accelerated corrosion testing. Each CPC also underwent physical characterization and launch-related compatibility testing . The initial results for the fifteen CPC systems are reported : Key words: corrosion preventive compound, CPC, spaceport, environmentally friendly, atmospheric exposure, marine, carbon steel, aluminum alloy, galvanic corrosion, wire on bolt.

The effect of corrosion product colloids on actinide transport

International Nuclear Information System (INIS)

Gardiner, M.P.; Smith, A.J.; Williams, S.J.

1992-01-01

The near field of the proposed UK repository for ILW/LLW will contain containers of conditioned waste in contact with a cementious backfill. It will contain significant quantities of iron and steel, Magnox and Zircaloy. Colloids deriving from their corrosion products may possess significant sorption capacity for radioelements. If the colloids are mobile in the groundwater flow, they could act as a significant vector for activity transport into the far field. The desorption of plutonium and americium from colloidal corrosion products of iron and zirconium has been studied under chemical conditions representing the transition from the near field to the far field. Desorption R d values of ≥ 5 x 10 6 ml g -1 were measured for both actinides on these oxides and hydroxides when actinide sorption took place under the near-field conditions and desorption took place under the far-field conditions. Desorption of the actinides occurred slowly from the colloids under far-field conditions when the colloids had low loadings of actinide and more quickly at high loadings of actinide. Desorbed actinide was lost to the walls of the experimental vessel. (author)

Solubility of corrosion products in high temperature water

International Nuclear Information System (INIS)

Srinivasan, M.P.; Narasimhan, S.V.

1995-01-01

A short review of solubility of corrosion products at high temperature in either neutral or alkaline water as encountered in BWR, PHWR and PWR primary coolant reactor circuits is presented in this report. Based on the available literature, various experimental techniques involved in the study of the solubility, theory for fitting the solubility data to the thermodynamic model and discussion of the published results with a scope for future work have been brought out. (author). 17 refs., 7 figs

77 FR 54891 - Certain Corrosion-Resistant Carbon Steel Flat Products from the Republic of Korea: Preliminary...

Science.gov (United States)

2012-09-06

... DEPARTMENT OF COMMERCE International Trade Administration [A-580-816] Certain Corrosion-Resistant...) is conducting the 18th administrative review of the antidumping order on corrosion-resistant carbon steel flat products (CORE) from the Republic of Korea \\1\\ (Korea). This review covers seven...

Establishing empirical relationships to predict porosity level and corrosion rate of atmospheric plasma-sprayed alumina coatings on AZ31B magnesium alloy

Directory of Open Access Journals (Sweden)

D. Thirumalaikumarasamy

2014-06-01

Full Text Available Plasma sprayed ceramic coatings are successfully used in many industrial applications, where high wear and corrosion resistance with thermal insulation are required. In this work, empirical relationships were developed to predict the porosity and corrosion rate of alumina coatings by incorporating independently controllable atmospheric plasma spray operational parameters (input power, stand-off distance and powder feed rate using response surface methodology (RSM. A central composite rotatable design with three factors and five levels was chosen to minimize the number of experimental conditions. Within the scope of the design space, the input power and the stand-off distance appeared to be the most significant two parameters affecting the responses among the three investigated process parameters. A linear regression relationship was also established between porosity and corrosion rate of the alumina coatings. Further, sensitivity analysis was carried out and compared with the relative impact of three process parameters on porosity level and corrosion rate to verify the measurement errors on the values of the uncertainty in estimated parameters.

High temperature corrosion in the thermochemical hydrogen production from nuclear heat

International Nuclear Information System (INIS)

Coen-Porisini, F.; Imarisio, G.

1976-01-01

In the production of hydrogen by water decomposition utilizing nuclear heat, a multistep process has to be employed. Water and the intermediate chemical products reach in chemical cycles giving hydrogen and oxygen with regeneration of the primary products used. Three cycles are examined, characterized by the presence of halide compounds and particularly hydracids at temperatures up to 800 0 C. Corrosion tests were carried out in hydrobromic acid, hydrochloric acid, ferric chloride solutions, and hydriodic acid

Improving by postoxidation of corrosion resistance of plasma nitrocarburized AISI 316 stainless steels

Science.gov (United States)

Yenilmez, A.; Karakan, M.; Çelik, İ.

2017-01-01

Austenitic stainless steels are widely used in several industries such as chemistry, food, health and space due to their perfect corrosion resistance. However, in addition to corrosion resistance, the mechanic and tribological features such as wear resistance and friction are required to be good in the production and engineering of this type of machines, equipment and mechanic parts. In this study, ferritic (FNC) and austenitic (ANC) nitrocarburizing were applied on AISI 316 stainless steel specimens with perfect corrosion resistance in the plasma environment at the definite time (4 h) and constant gas mixture atmosphere. In order to recover corrosion resistance which was deteriorated after nitrocarburizing again, plasma postoxidation process (45 min) was applied. After the duplex treatment, the specimens' structural analyses with XRD and SEM methods, corrosion analysis with polarization method and surface hardness with microhardness method were examined. At the end of the studies, AISI 316 surface hardness of stainless steel increased with nitrocarburizing process, but the corrosion resistance was deteriorated with FNC (570 °C) and ANC (670 °C) nitrocarburizing. With the following of the postoxidation treatment, it was detected that the corrosion resistance became better and it approached its value before the process.

Siderite as a Corrosion Product on Archaeological Iron from a Waterlogged Environment

DEFF Research Database (Denmark)

Matthiesen, H.; Hilbert, Lisbeth Rischel; Gregory, D.J.

2003-01-01

This paper discusses the occurrence of siderite (FeCO3) on iron artifacts excavated from the waterlogged peat and gyttja sediment of the Danish Iron Age site Nydam Mose. Siderite was identified by means of X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FTIR) and scanning electron...... microscopy with energy-dispersive spectrometry (SEM-EDS), which showed only minor contents of other minerals in the corrosion scales. The implications of the formation of siderite as a corrosion product are discussed in terms of its possible passivating properties and thermodynamic stability in situ...

The marine corrosion program developed by Nuclebras

International Nuclear Information System (INIS)

Moreira, P.A.P.; Quinan, M.A.

1986-01-01

A marine corrosion program is being developed by NUCLEBRAS and NUCLEN. This program consists in carrying out non-accelerated experiments in marine atmosphere, with immersion in sewater and laboratory accelerated tests. The purpose is to obtain a correlation between the corrosion rates observed in non-accelerated conditions and laboratory tests. Through these results it is inteded, only with laboratory tests, to estimate the bahavior of similar materials when tsted in similar marine atmosphereic conditions. Some aspects observed in the implementation of the program and some results so far obtained are discussed. (Author) [pt

XPS response in the corrosion products analysis for copper exposed at clean air environment

International Nuclear Information System (INIS)

Mariaca, L.; Morcillo, M.; Feliu Jr, S.; Gonzalez, J.A.

1998-01-01

In this work is presented the obtained response for superficial analysis technique by X-ray photoelectron spectroscopy (XPS or ESCA), to determine the corrosion products formed during the copper exposure at environment without pollutants (clean air) at 50, 70 and 90 % of relative humidity at 35 Centigrade. One of the copper corrosion products most knew is Cu 2 O. This oxide is formed instantly to be exposed the copper at air. However in function of the exposure time and the relative humidity at it is exposed, the Cu 2 O oxide is transformed at Cu O and Cu(OH) 2 (Author)

Corrosion resistance of metals and alloys in molten alkalies

International Nuclear Information System (INIS)

Zarubitskij, O.G.; Dmitruk, B.F.; Minets, L.A.

1979-01-01

Literature data on the corrosion of non-ferrous and noble metals, iron and steels in the molten alkalis and mixtures of their base are presented. It is shown that zirconium, niobium and tantalum are characterized by high corrosion stability in the molten NaOH. Additions of NaOH and KOH to the alkali chloride melts result in a 1000 time decrease of zirconium corrosion rate at 850 deg. The data testify to the characteristic passivating properties of OH - ions; Mo and W do not possess an ability to selfpassivation in hydroxide melts. Corrosion resistance of carbon and chromium-nickel steels in hydroxide melts depends considerably on the temperature, electrolyte composition and atmosphere over them. At the temperatures up to 600 deg C chromium-nickel steel is corrosion resistant in the molten alkali only in the inert atmosphere. Corrosion rate of chromium-nickel alloy is the lower the less chromium and the more nickel it contains. For the small installations the 4Kh18N25S2 and Kh23N28M3D3T steels can be recommended

Evaluation of protective effect of deposits formed by naphthenic corrosion and sulfidation on carbon steel and steel 5Cr-0.5Mo exposed in atmospheric distillation fractions

Directory of Open Access Journals (Sweden)

Gloria Duarte

2017-05-01

Full Text Available Refining of so-called opportunity crude oils with a high level of naphthenic acids and sulfur compounds has been increasing interest due to limited availability of light crude oils, however, considerable corrosive effects in the processing to high temperature on pipes and distillation towers mainly by the attack of naphthenic acids and sulfur compounds; sulfur compounds could be corrosive or can reduce the attack of naphthenic acids due to the formation of sulfides layers on the metal surface. In this work was evaluated the performance of deposits formed on the surface of carbon steel AISI SAE 1020 and 5% Cr-0.5% Mo steel exposed in crude oil fractions obtained from atmospheric distillation tower. For this, gravimetric tests were performed in dynamic autoclave using metal samples pre-treated in a crude oil fraction obtained from the atmospheric distillation tower of the Crude Distillation Unit (CDU # 1 in order to form layers of sulfides on the surface of the two materials and subsequently to expose pre-treated and non-pretreated samples in two different crude oil fractions obtained from atmospheric distillation tower of Crude Distillation Unit (CDU # 2. The evaluation showed that the samples pretreated decreased tendency to corrosion by naphthenic acids and sulfidation compared to untreated samples.

Atmospheric-Induced Stress Corrosion Cracking of Grade 2205 Duplex Stainless Steel—Effects of 475 °C Embrittlement and Process Orientation

Directory of Open Access Journals (Sweden)

Cem Örnek

2016-07-01

Full Text Available The effect of 475 °C embrittlement and microstructure process orientation on atmospheric-induced stress corrosion cracking (AISCC of grade 2205 duplex stainless steel has been investigated. AISCC tests were carried out under salt-laden, chloride-containing deposits, on U-bend samples manufactured in rolling (RD and transverse directions (TD. The occurrence of selective corrosion and stress corrosion cracking was observed, with samples in TD displaying higher propensity towards AISCC. Strains and tensile stresses were observed in both ferrite and austenite, with similar magnitudes in TD, whereas, larger strains and stresses in austenite in RD. The occurrence of 475 °C embrittlement was related to microstructural changes in the ferrite. Exposure to 475 °C heat treatment for 5 to 10 h resulted in better AISCC resistance, with spinodal decomposition believed to enhance the corrosion properties of the ferrite. The austenite was more susceptible to ageing treatments up to 50 h, with the ferrite becoming more susceptible with ageing in excess of 50 h. Increased susceptibility of the ferrite may be related to the formation of additional precipitates, such as R-phase. The implications of heat treatment at 475 °C and the effect of process orientation are discussed in light of microstructure development and propensity to AISCC.

Effect of flue gas composition on deposit induced high temperature corrosion under laboratory conditions mimicking biomass firing. Part I: Exposures in oxidizing and chlorinating atmospheres

DEFF Research Database (Denmark)

Okoro, Sunday Chukwudi; Kiamehr, Saeed; Montgomery, Melanie

2017-01-01

on hightemperature corrosion of an austenitic superheater material under laboratoryconditions mimicking biomass firing is investigated in this work. Exposuresinvolving deposit (KCl)-coated and deposit-free austenitic stainless steel (TP347H FG) samples were conducted isothermally at 560 8C for 72 h, under...... only in an oxidizing-chlorinating atmosphere, otherwise corrosionresults in formation of a duplex oxide. Corrosion attack on deposit-coatedsamples was higher than on deposit-free samples irrespective of the gaseousatmosphere. Specifically, severe volatilization of alloying elements occurred ondeposit-coated...

Corrosion of metal iron in contact with anoxic clay at 90 °C: Characterization of the corrosion products after two years of interaction

International Nuclear Information System (INIS)

Schlegel, Michel L.; Bataillon, Christian; Brucker, Florence; Blanc, Cécile; Prêt, Dimitri; Foy, Eddy; Chorro, Matthieu

2014-01-01

Highlights: • Generalized, heterogeneous corrosion is observed. • The corrosion interface is made of several layers with distinct mineralogy. • Magnetite, chukanovite, Fe-phyllosilicate, ankerite are identified from metal to clay. • The estimated corrosion damage (15 μm in two years) supports surface passivation. • The corrosion products contain only half of oxidized Fe. - Abstract: Chemical and mineralogical properties of solids formed upon free corrosion of two iron probes (one massive iron rod, and one model overpack made by two pipes covering the ends of a glass rod) in saturated clay rock (Callovo-Oxfordian formation, East of Paris Basin, France) at 90 °C over two years were investigated by microscopic and spectroscopic techniques (X-ray tomography, scanning electron microscopy coupled with energy-dispersive X-ray analysis, Raman microspectroscopy, micro-X-ray diffraction, and micro-X-ray Absorption Fine Structure spectroscopy). The corrosion rate of the massive rod was monitored in situ by electrochemical impedance spectrometry, and found to decrease from about 90 μm/year during the first month of reaction, to less than 1 μm/year after two years. X-ray tomography revealed the presence of several fractures suggesting the presence of preferential flow and diffusion pathways along the iron samples. Microscopic observations revealed similar corrosion interfaces for both samples. Corrosion heterogeneously affected the interface, with damaged thickness from ∼0 to 80 μm. In extensively damaged areas, an inner discontinuous layer of magnetite in contact with metal, an intermediate chukanovite (Fe 2 CO 3 (OH) 2 ) layer (only when magnetite is present, and only for the overpack), and an outer layer of poorly ordered Fe phyllosilicate were observed. In areas with little damage, only the Fe-silicate solids are observed. The clay transformation layer is predominantly made of ankerite ((Fe,Ca,Mg)CO 3 ) forming a massive unit near the trace of the original

78 FR 70076 - Aging Management of Internal Surfaces, Fire Water Systems, Atmospheric Storage Tanks, and...

Science.gov (United States)

2013-11-22

... Systems, Atmospheric Storage Tanks, and Corrosion Under Insulation AGENCY: Nuclear Regulatory Commission... Internal Surfaces, Fire Water Systems, Atmospheric Storage Tanks, and Corrosion Under Insulation.'' This LR... related to internal surface aging effects, fire water systems, atmospheric storage tanks, and corrosion...

Corrosion product balances for the Ringhals PWR plants based on extensive fuel crud and water chemistry measurements

International Nuclear Information System (INIS)

Lundgren, K.; Wikmark, G.; Bengtsson, B.

2010-01-01

The corrosion product balance in a PWR plant is of great importance for the fuel performance as well as for the radiation field buildup. This balance is of special concern in connection to steam generator replacement (SGR) and power uprate projects. The Ringhals PWRs are all of Westinghouse design. Two of the plants have performed Steam Generator Replacement (SGR) to I-690 SG tubes and such a replacement is being planned in the third and last unit in 2011. Two of the units are in different phases of power uprate projects. The plants are all on 10-14-months cycles operating with medium to high fuel duty. Water chemistry is controlled by a pH300 in the range ∼7.2 to 7.4 from beginning of cycle to end of cycle (BOC-EOC) in the units with new SGs while kept at a coordinated pH of 7.2 in the one still using I-600. The maximum Li content has recently been increased to about 4.5 to 5 ppm in all units. In order to be able to improve the assessment of corrosion product balances in the plants, comprehensive fuel crud measurements were performed in 2007. Improved integrated reactor water sampling techniques have also been introduced in order to make accurate mass balances possible. The corrosion products covered in the study are the main constituents, Ni, Fe and Cr in the primary circuit Inconel and stainless steel, together with Co. The activated corrosion products, Co-58, Co-60, Cr-51, Fe-59 and Mn-54, are all mainly produced through neutron irradiation of the covered corrosion products. The main results of the corrosion product balances are presented. Observed differences between the plants, indicating significant impact of pH control and SG tube materials, are presented and discussed. The importance of accurate sampling techniques is especially addressed in this paper. (author)

Release of corrosion products from construction materials containing cobalt. Pt.2: Inconel X750

International Nuclear Information System (INIS)

Falk, I.

1978-02-01

This report describes experimental work aimed at determining the release rate for corrosion products from 18Cr8Ni steel and Inconel X750 in BWR environments. For test purposes these environments were simulated in a high pressure loop, where irradiated samples of the materials were exposed for 720 hours. The amounts of released products were determined using gamma spectrometric analysis. The results show that the release from Inconel X750 is higher than that from 18Cr8Ni steel. The release calculated from Co58 measurements is 7 times higher and from Co60 measurements it is 1.5 times higher. Both the filtered and the deposited fractions of the released corrosion products exhibit the same relative concentrations of Co58 and Co60. (author)

Effects of environmental variables on the crack initiation stages of corrosion fatigue of high strength aluminum alloys

Science.gov (United States)

Poteat, L. E.

1981-01-01

Fatigue initiation in six aluminum alloys used in the aircraft industry was investigated. Cyclic loading superimposed on a constant stress was alternated with atmospheric corrosion. Tests made at different stress levels revealed that a residual stress as low as 39% of the yield strength caused stress corrosion cracking in some of the alloys. An atmospheric corrosion rate meter developed to measure the corrosivity of the atmosphere is described. An easily duplicated hole in the square test specimen with a self-induced residual stress was developed.

Guidelines for prediction of CO{sub 2} corrosion in oil and gas production systems

Energy Technology Data Exchange (ETDEWEB)

Nyborg, Rolf

2009-09-15

A group of corrosion experts from different oil companies has prepared guidelines for use of CO{sub 2} corrosion prediction tools. The guidelines are intended for use in design and engineering practice applied by companies operating oil and gas production facilities. This document attempts to set minimum guidelines that should be common to most companies. The document is sufficiently flexible to allow individual companies to adapt the information set forth in this document to their own environment and requirements. A methodology for defining the Iikelihood of corrosion and the impact on CO{sub 2} prediction is developed. The CO{sub 2} prediction is based on existing tools. An overview of available CO{sub 2} corrosion prediction models evaluated by the participants is given. It is the responsibility of the operator to select which model to use. (Author)

Grain boundary defects initiation at the outer surface of dissimilar welds: corrosion mechanism studies

International Nuclear Information System (INIS)

De Bouvier, O.; Yrieix, B.

1995-11-01

Dissimilar welds located on the primary coolant system of the French PWR I plants exhibit grain boundary defects in the true austenitic zones of the first buttering layer. If grain boundaries reach the interface, they can extend to the martensitic band. Those defects are filled with compact oxides. In addition, the ferritic base metal presents some pits along the interface. Nowadays, three mechanisms are proposed to explain the initiation of those defects: stress corrosion cracking, intergranular corrosion and high temperature intergranular oxidation. This paper is dealing with the study of the mechanisms involved in the corrosion phenomenon. Intergranular corrosion tests performed on different materials show that only the first buttering layer, even with some δ ferrite, is sensitized. The results of stress corrosion cracking tests in water solutions show that intergranular cracking is possible on a bulk material representative of the first buttering layer. It is unlikely on actual dissimilar welds where the ferritic base metal protects the first austenitic layer by galvanic coupling. Therefore, the stress corrosion cracking assumption cannot explain the initiation of the defects in aqueous environment. The results of the investigations and of the corrosion studies led to the conclusion that the atmosphere could be the only possible aggressive environment. This conclusion is based on natural atmospheric exposure and accelerated corrosion tests carried out with SO 2 additions in controlled atmosphere. They both induce a severe intergranular corrosion on true sensitized austenitic materials. This corrosion studies cannot conclude definitively on the causes of the defect initiation on field, but they show that the atmospheric corrosion could produce intergranular attacks in the pure austenitic zones of the first buttering layer of the dissimilar welds and that this corrosion is stress assisted. (author). 1 ref., 6 figs., 4 tabs

75 FR 55769 - Certain Corrosion-Resistant Carbon Steel Flat Products From the Republic of Korea: Notice of...

Science.gov (United States)

2010-09-14

... DEPARTMENT OF COMMERCE International Trade Administration [A-580-816] Certain Corrosion-Resistant...) is conducting the sixteenth administrative review of the antidumping order on corrosion-resistant carbon steel flat products (CORE) from the Republic of Korea (Korea).\\1\\ This review covers eight...

77 FR 14501 - Certain Corrosion-Resistant Carbon Steel Flat Products From the Republic of Korea: Notice of...

Science.gov (United States)

2012-03-12

... DEPARTMENT OF COMMERCE International Trade Administration [A-580-816] Certain Corrosion-Resistant... the preliminary results of the antidumping duty administrative review for certain corrosion-resistant carbon steel flat products (CORE) from the Republic of Korea (Korea).\\1\\ This review covers eight...

Corrosion of Steel in Concrete, Part I – Mechanisms

DEFF Research Database (Denmark)

Küter, André; Møller, Per; Geiker, Mette Rica

2006-01-01

prematurely. Reinforcement corrosion is identified to be the foremost cause of deterioration. Steel in concrete is normally protected by a passive layer due the high alkalinity of the concrete pore solution; corrosion is initiated by neutralization through atmospheric carbon dioxide and by ingress...... of depassivation ions, especially chloride ions. The background and consequences of deterioration of reinforced concrete structures caused by steel corrosion are summarized. Selected corrosion mechanisms postulated in the literature are briefly discussed and related to observations. The key factors controlling...... initiation and propagation of corrosion of steel in concrete are outlined....

Study of the corrosion products in the primary system of PWR plants as the source of radiation fields build-up

International Nuclear Information System (INIS)

Brabant, R. van; Regge, P. de.

1982-01-01

In the first part the behaviour of the corrosion products in the primary system of PWR plants is depicted on the basis of a literature review of the field. Water chemistry, corrosion processes and activation of corrosion products are the main topics. In the second part the results of the characterization of corrosion particles in the primary coolant circuit of the Doel 1 and 2 reactors are described, during steady state operation and transient phases. In the third part the possibilities for radiation control at nuclear power plants are outlined. The filtration possibilities for the reactor coolant are explored in detail. (author)

Analysis of Gamma Dose Rate Caused by Corrosion Products inside the Containment Building of Yonngwang Nuclear Power Plant Unit 3 During Shutdown Period

Energy Technology Data Exchange (ETDEWEB)

Ha, Wi Ho; Kim, Jae Cheon; Kim, Soon Young; Kim, Jong Kyung [Hanyang Univ., Seoul (Korea, Republic of)

2005-07-01

Occupational radiation exposure(ORE) of nuclear power plant(NPP) workers mainly occurs during the shutdown period. Major radioactive sources are the corrosion products released from the reactor coolant system(RCS). The corrosion products consist of circulating crud and deposited crud. Major radioactive corrosion products, {sup 58}Co and {sup 60}Co, are known to contribute approximately more than 70% of the total ORE. In this study, the corrosion products regarding cobalt were evaluated during the shutdown period, and gamma dose rates caused by them were calculated at the main working area inside the containment building of the Yonggwang NPP Unit 3.

Kinetics of corrosion products release from nickel-base alloys corroding in primary water conditions. A new modeling of release

International Nuclear Information System (INIS)

Carrette, F.; Guinard, L.; Pieraggi, B.

2002-01-01

The radioactivity in the primary circuit arises mainly from the activation of corrosion products in the core of pressurised water reactors; corrosion products dissolve from the oxide scales developed on steam generator tubes of alloy 690. The controlling and modelling of this process require a detailed knowledge of the microstructure and chemical composition of oxide scales as well as the kinetics of their corrosion and dissolution. Alloy 690 was studied as tubes and sheets, with three various surface states (as-received, cold-worked, electropolished). Corrosion tests were performed at 325 C and 155 bar in primary water conditions (B/Li - 1000/2 ppm, [H 2 ] 30 cm 3 .kg -1 TPN, [O 2 ] < 5 ppb); test durations ranged between 24 and 2160 hours. Corrosion tests in the TITANE loop provided mainly corrosion and oxidation kinetics, and tests in the BOREAL loop yielded release kinetics. This study revealed asymptotic type kinetics. Characterisation of the oxide scales grown in representative conditions of the primary circuit was performed by several techniques (SEM, TEM, SIMS, XPS, GIXRD). These analyses revealed the essential role of the fine grained cold-worked scale present on as-received and cold-worked materials. This scale controls the corrosion and release phenomena. The kinetic study and the characterisation of the oxide scales contributed to the modelling of the corrosion/release process. A growth/dissolution model was proposed for corrosion product scales grown in non-saturated dynamic fluid. This model provided the temporal evolution of oxide scales and release kinetics for different species (Fe, Ni, Cr). The model was validated for several surface states and several alloys. (authors)

Corrosion behavior of corrosion resistant alloys in stimulation acids

Energy Technology Data Exchange (ETDEWEB)

Cheldi, Tiziana [ENI E and P Division, 20097 San Donato Milanese Milano (Italy); Piccolo, Eugenio Lo; Scoppio, Lucrezia [Centro Sviluppo Materiali, via Castel Romano 100, 00128 Rome (Italy)

2004-07-01

In the oil and gas industry, selection of CRAs for downhole tubulars is generally based on resistance to corrosive species in the production environment containing CO{sub 2}, H{sub 2}S, chloride and in some case elemental sulphur. However, there are non-production environments to which these materials must also be resistant for either short term or prolonged duration; these environments include stimulation acids, brine and completion fluids. This paper reports the main results of a laboratory study performed to evaluate the corrosion and stress corrosion behaviour to the acidizing treatments of the most used CRAs for production tubing and casing. Laboratory tests were performed to simulate both 'active' and 'spent' acids operative phases, selecting various environmental conditions. The selected steel pipes were a low alloyed steel, martensitic, super-martensitic, duplex 22 Cr, superduplex 25 Cr and super-austenitic stainless steels (25 Cr 35 Ni). Results obtained in the 'active' acid environments over the temperature range of 100-140 deg. C, showed that the blend acids with HCl at high concentration and HCl + HF represented too much severe conditions, where preventing high general corrosion and heavy localised corrosion by inhibition package becomes very difficult, especially for duplex steel pipe, where, in some case, the specimens were completely dissolved into the solution. On the contrary, all steels pipes were successfully protected by inhibitor when organic acid solution (HCOOH + CH{sub 3}COOH) were used. Furthermore, different effectiveness on corrosion protection was showed by the tested inhibitors packages: e.g. in the 90% HCl at 12% + 10 CH{sub 3}COOH acid blend. In 'spent' acid environments, all steel pipes showed to be less susceptible to the localised and general corrosion attack. Moreover, no Sulphide Stress Corrosion Cracking (SSC) was observed. Only one super-austenitic stainless steel U-bend specimen showed

Synergy effect of naphthenic acid corrosion and sulfur corrosion in crude oil distillation unit

Energy Technology Data Exchange (ETDEWEB)

Huang, B.S., E-mail: yinwenfeng2010@163.com [College of Materials Science and Engineering, Southwest Petroleum University, Sichuan, Chengdu, 610500 (China); Yin, W.F. [College of Mechatronic Engineering, Southwest Petroleum University, Sichuan, Chengdu, 610500 (China); Sang, D.H. [Sheng Li Construction Group International Engineering Department, Shandong, Dongying, 257000 (China); Jiang, Z.Y. [College of Materials Science and Engineering, Southwest Petroleum University, Sichuan, Chengdu, 610500 (China)

2012-10-15

Highlights: Black-Right-Pointing-Pointer The corrosion of a carbon-manganese steel and a stainless steel in sulfur and/or naphthenic acid media was investigated. Black-Right-Pointing-Pointer The corrosion rate of the carbon-manganese steel increased with the increase of the acid value and sulfur content. Black-Right-Pointing-Pointer The critical values of the concentration of sulfur and acid for corrosion rate of the stainless steel were ascertained respectively. Black-Right-Pointing-Pointer The stainless steel is superior to the carbon-manganese steel in corrosion resistance because of the presence of stable Cr{sub 5}S{sub 8} phases. - Abstract: The synergy effect of naphthenic acid corrosion and sulfur corrosion at high temperature in crude oil distillation unit was studied using Q235 carbon-manganese steel and 316 stainless steel. The corrosion of Q235 and 316 in corrosion media containing sulfur and/or naphthenic acid at 280 Degree-Sign C was investigated by weight loss, scanning electron microscope (SEM), EDS and X-ray diffractometer (XRD) analysis. The results showed that in corrosion media containing only sulfur, the corrosion rate of Q235 and 316 first increased and then decreased with the increase of sulfur content. In corrosion media containing naphthenic acid and sulfur, with the variations of acid value or sulfur content, the synergy effect of naphthenic acid corrosion and sulfur corrosion has a great influence on the corrosion rate of Q235 and 316. It was indicated that the sulfur accelerated naphthenic acid corrosion below a certain sulfur content but prevented naphthenic acid corrosion above that. The corrosion products on two steels after exposure to corrosion media were investigated. The stable Cr{sub 5}S{sub 8} phases detected in the corrosion products film of 316 were considered as the reason why 316 has greater corrosion resistance to that of Q235.

78 FR 55057 - Corrosion-Resistant Carbon Steel Flat Products from the Republic of Korea: Preliminary Results of...

Science.gov (United States)

2013-09-09

... DEPARTMENT OF COMMERCE International Trade Administration [A-580-816] Corrosion-Resistant Carbon... Department) is conducting an administrative review of the antidumping duty order on corrosion-resistant carbon steel flat products (CORE) from the Republic of Korea (Korea), covering the period [[Page 55058...

78 FR 16247 - Corrosion-Resistant Carbon Steel Flat Products From the Republic of Korea; Final Results of...

Science.gov (United States)

2013-03-14

... DEPARTMENT OF COMMERCE International Trade Administration [A-580-816] Corrosion-Resistant Carbon... preliminary results of the administrative review of the antidumping duty order on corrosion-resistant carbon steel flat products (CORE) from the Republic of Korea (Korea).\\1\\ This review covers seven manufacturers...

76 FR 4291 - Corrosion-Resistant Carbon Steel Flat Products From the Republic of Korea: Partial Rescission of...

Science.gov (United States)

2011-01-25

... DEPARTMENT OF COMMERCE International Trade Administration [C-580-818] Corrosion-Resistant Carbon... Commerce (the Department) initiated an administrative review of the countervailing duty order on corrosion- resistant carbon steel flat products from the Republic of Korea covering the period January 1, 2009, through...

Major activated corrosion products cobalt, silver and antimony in the primary coolant of PWR power plants

International Nuclear Information System (INIS)

Xu Mingxia

2012-01-01

The production of the major activated corrosion products such as cobalt, silver and antimony in the primary coolant of PWR power plants and the impacts on the increase of the dose rates caused by these corrosion products during the shutdown are described in the paper. Investigating the corrosion product behavior during the operation and shutdown periods aims at detecting the appearance of these radiological pollutants in the early time and searching relevant solutions that may enable eventually to decrease the dose rate. The solutions may include: Replacing critical material in the primary system's equipment and components, which contact with primary coolant circuit to possibly limit the source term, Elaborating strictly the specific chemical and shutdown procedure to optimize the purification capacity and to minimize the over-contaminations; Improving purification techniques according to the real operation circumstance, and limiting the impacts of these pollutants. It is obvious in the real practices that implementing appropriate solution will be benefit to decrease or limit the pollutants species like cobalt, silver and antimony. (author)

NASA's Corrosion Technology Laboratory at the Kennedy Space Center: Anticipating, Managing, and Preventing Corrosion

Science.gov (United States)

Calle, Luz Marina

2014-01-01

Corrosion is the degradation of a material that results from its interaction with the environment. The marine environment at NASAs Kennedy Space Center (KSC) has been documented by ASM International (formerly American Society for Metals) as the most corrosive in the United States. With the introduction of the Space Shuttle in 1981, the already highly corrosive conditions at the launch pads were rendered even more severe by the 70 tons of highly corrosive hydrochloric acid that were generated by the solid rocket boosters. Numerous failures at the launch pads are caused by corrosion.The structural integrity of ground infrastructure and flight hardware is critical to the success, safety, cost, and sustainability of space missions. As a result of fifty years of experience with launch and ground operations in a natural marine environment that is highly corrosive, NASAs Corrosion Technology Laboratory at KSC is a major source of corrosion control expertise in the launch and other environments. Throughout its history, the Laboratory has evolved from what started as an atmospheric exposure facility near NASAs launch pads into a world-wide recognized capability that provides technical innovations and engineering services in all areas of corrosion for NASA and external customers.This presentation will provide a historical overview of the role of NASAs Corrosion Technology in anticipating, managing, and preventing corrosion. One important challenge in managing and preventing corrosion involves the detrimental impact on humans and the environment of what have been very effective corrosion control strategies. This challenge has motivated the development of new corrosion control technologies that are more effective and environmentally friendly. Strategies for improved corrosion protection and durability can have a huge impact on the economic sustainability of human spaceflight operations.

Airborne bacteria associated with corrosion of mild steel 1010 and aluminum alloy 1100.

Science.gov (United States)

Rajasekar, Aruliah; Xiao, Wang; Sethuraman, Manivannan; Parthipan, Punniyakotti; Elumalai, Punniyakotti

2017-03-01

A novel approach to measure the contribution of airborne bacteria on corrosion effects of mild steel (MS) and aluminum alloy (AA) as a function of their exposure period, and the atmospheric chemical composition was investigated at an urban industrial coastal site, Singapore. The 16S rRNA and phylogenetic analyses showed that Firmicutes are the predominant bacteria detected in AA and MS samples. The dominant bacterial groups identified were Bacillaceae, Staphylococcaceae, and Paenibacillaceae. The growth and proliferation of these bacteria could be due to the presence of humidity and chemical pollutants in the atmosphere, leading to corrosion. Weight loss showed stronger corrosion resistance of AA (1.37 mg/cm 2 ) than MS (26.13 mg/cm 2 ) over the exposure period of 150 days. The higher corrosion rate could be a result of simultaneous action of pollutants and bacterial exopolysaccharides on the metal surfaces. This study demonstrates the significant involvement of airborne bacteria on atmospheric corrosion of engineering materials.

Enhanced corrosion resistance of stainless steel type 316 in sulphuric acid solution using eco-friendly waste product

Science.gov (United States)

Sanni, O.; Popoola, A. P. I.; Fayomi, O. S. I.

2018-06-01

Literature has shown that different organic compounds are effective corrosion inhibitors for metal in acidic environments. Such compounds usually contain oxygen, nitrogen or sulphur and function through adsorption on the metal surface, thereby creating a barrier for corrosion attack. Unfortunately, these organic compounds are toxic, scarce and expensive. Therefore, plants, natural product and natural oils have been posed as cheap, environmentally acceptable, abundant, readily available and effective molecules having low environmental impact. The corrosion resistance of austenitic stainless steel Type 316 in the presence of eco-friendly waste product was studied using weight loss and potentiodynamic polarization techniques in 0.5 M H2SO4. The corrosion rate and corrosion potential of the steel was significantly altered by the studied inhibitor. Results show that increase in concentration of the inhibitor hinders the formation of the passive film. Experimental observation shows that its pitting potential depends on the concentration of the inhibitor in the acid solution due to adsorption of anions at the metal film interface. The presence of egg shell powder had a strong influence on the corrosion resistance of stainless steel Type 316 with highest inhibition efficiency of 94.74% from weight loss analysis, this is as a result of electrochemical action and inhibition of the steel by the ionized molecules of the inhibiting compound which influenced the mechanism of the redox reactions responsible for corrosion and surface deterioration. Inhibitor adsorption fits the Langmuir isotherm model. The two methods employed for the corrosion assessment were in good agreement.

Modelling the behaviour of corrosion products in the primary heat transfer circuits of pressurised water reactors

International Nuclear Information System (INIS)

Rodliffe, R.S.; Polley, M.V.; Thornton, E.W.

1985-05-01

The redistribution of corrosion products from the primary circuit surfaces of a water reactor can result in increased flow resistance, poorer heat transfer performance, fuel failure and radioactive contamination of circuit surfaces. The environment is generally sufficiently well controlled to ensure that the first three effects are not limiting. The last effect is of particular importance since radioactive corrosion products are major contributors to shutdown fields and since it is necessary to ensure that the radiation exposure of personnel is as low as reasonably achievable. This review focusses attention on the principles which must form the basis for any mechanistic model describing the formation, transport and deposition of radioactive corrosion products. It is relevant to all water reactors in which the primary heat transfer medium is predominantly single-phase water and in which steam is generated in a secondary circuit, i.e. including CANDU pressurised heavy water reactors, Sovient VVERs, etc. (author)

X-ray diffraction phase analysis of crystalline copper corrosion products after treatment in different chloride solutions

International Nuclear Information System (INIS)

Chmielova, M.; Seidlerova, J.; Weiss, Z.

2003-01-01

The corrosion products Cu 2 (OH) 3 Cl, Cu 2 O, and CuCl 2 were identified on the surface of copper plates after their four days treating in three different sodium chloride, sodium/magnesium, and sodium/calcium chloride solutions using X-ray diffraction powder analysis. However, the quantitative proportions of individual corrosion products differ and depend on the type of chloride solution used. Treating of copper plates only in the sodium chloride solution produced the mixture of corrosion products where Cu 2 O is prevailing over the Cu 2 (OH) 3 Cl and CuCl 2 was not identified. The sample developed after treating of the cooper surface in the sodium/magnesium chloride solution contains Cu 2 (OH) 3 Cl and CuCl 2 prevailing over the Cu 2 O, while the sample developed after treatment of copper in sodium/calcium chloride solution contains Cu 2 (OH) 3 Cl prevailing over CuCl 2 and Cu 2 O was not identified

Activity of corrosion products in pool type reactors with ascending flow in the core

International Nuclear Information System (INIS)

Andrade e Silva, Graciete S. de; Queiroz Bogado Leite, Sergio de

1995-01-01

A model for the activity of corrosion products in the water of a pool type reactor with ascending flow is presented. The problem is described by a set of coupled differential equations relating the radioisotope concentrations in the core and pool circuits and taking into account two types of radioactive sources: i) those from radioactive species formed in the fuel cladding, control elements, reflector, etc, and afterwards released to the primary stream by corrosion (named reactor sources) and ii) those formed from non radioactive isotopes entering the primary stream by corrosion of the circuit components and being activated when passing through the core (named circuit sources). (author). 6 refs, 3 figs, 4 tabs

Semiquantitative analysis of corrosion products in iron channel by the X-ray diffraction technique

International Nuclear Information System (INIS)

Bueno, C.R.E.; Varela, J.A.

1995-01-01

The corrosion in the us very important in the slag line region, but in others regions over and above this line there is a corrosion process still important. We have made a detailed mapping of phases present in seven different regions in the iron channel in three distinct positions. After the phases identifications, it was made a deconvolution of the diffractograms using Gaussian functions. The analysis of the relative intensity of each phase gave an idea for a semi-quantitative analysis and we have proposed a mechanism of the refractory corrosion. It was observed that the calcium oxide migrates by diffusion to different regions originating low melting point products like pseudo-wolastonite, anorthite and guelenite. (author)

78 FR 59652 - Certain Corrosion-Resistant Carbon Steel Flat Products From the Republic of Korea: Notice of...

Science.gov (United States)

2013-09-27

... DEPARTMENT OF COMMERCE International Trade Administration [A-580-816] Certain Corrosion-Resistant... corrosion-resistant carbon steel flat products (``CORE'') from the Republic of Korea (``Korea''), pursuant... administrative review of the antidumping duty order on CORE from Korea covering the period of review (``POR'') of...

76 FR 77775 - Corrosion-Resistant Carbon Steel Flat Products from the Republic of Korea: Extension of Time...

Science.gov (United States)

2011-12-14

... DEPARTMENT OF COMMERCE International Trade Administration [C-580-818] Corrosion-Resistant Carbon... results of the administrative review of the countervailing duty order on corrosion-resistant carbon steel flat products from the Republic of Korea covering the period January 1, 2009, through December 31, 2009...

78 FR 59651 - Certain Corrosion-Resistant Carbon Steel Flat Products From the Republic of Korea: Notice of...

Science.gov (United States)

2013-09-27

... DEPARTMENT OF COMMERCE International Trade Administration [A-580-816] Certain Corrosion-Resistant... duty order on certain corrosion-resistant carbon steel flat products (``CORE'') from the Republic of... covering the period of review (``POR'') of August 1, 2006 through July 31, 2007, with respect to the...

The effect of brazing parameters on corrosion behavior of brazed aluminum joints

Science.gov (United States)

Ghasimakbari, Farzam; Hadian, Ali Mohammad; Ershadrad, Soheil; Omidazad, Amir Mansour

2018-01-01

Fluid transmission pipes made of aluminum are widely used in petrochemical industries. For many applications, they have to be brazed to each other. The brazed joints, in many cases, are encountered with corrosive medias. This paper reports a part of a work to investigate the corrosion behavior of brazed AA6061 using AA4047 as filler metal with and without the use of flux under different brazing atmospheres. The samples brazed under air, vacuum, argon, and hydrogen atmospheres. The interfacial area of the joints was examined to ensure being free of any defects. The sides of each test piece were covered with an insulator and the surface of the joint was encountered to polarization test. The results revealed a significant difference of corrosion resistance. The samples that brazed under argon and hydrogen atmospheres had better corrosion resistance than other samples. The microstructure of the corroded joints revealed that the presence of defects, impurities due to use of flux and depth of filter metal penetration in base metal are crucial variables on the corrosion resistance of the joints.

Corrosion of aluminum and zinc in containment following a LOCA and potential for precipitation of corrosion products in the sump

International Nuclear Information System (INIS)

Niyogi, K.K.; Lunt, R.R.; Mackenzie, J.S.

1982-01-01

Following a loss-of-coolant accident (LOCA) in a LWR containment, certain materials in the containment come in contact with alkaline emergency cooling and containment spray solutions and may corrode yielding hydrogen gas. The problems associated with the production of hydrogen gas and the control of combustible gas concentration have been extensively explored in recent years. However, the phenomenon of corrosion and its consequences in the long term cooling of the reactor and the containment have drawn very little attention. United Engineers and Constructors Inc. has made an extensive effort to study through literature survey the solubility of the corrosion products from aluminum and zinc in order to assess the potential for precipitation in the containment sump. The analysis presented in this article is based on parameters for a typical large dry reactor containment with caustic/boric acid buffered spray solution. Parameters used in this study may vary from one plant to another. However, they are not expected to affect the overall conclusions

Reduction of air pollutants - a tool for control of atmospheric corrosion

Directory of Open Access Journals (Sweden)

Kucera, V.

2003-12-01

Full Text Available In most urban areas in Europe and Northern America serious corrosion impacts on buildings and cultural monuments have been caused by emissions of pollutants. The rapidly increasing pollution levels in many of the developing countries also exert a serious threat to materials. Beside the very important role of SO₂ also the direct or synergistic effect of NO_x and O₃, the particulates and rain acidity may contribute in an important way to materials degradation. Results from extensive international field exposure programs i.e. within the UN/ECE have enabled development of dose-response relations which describe the effect of dry and wet deposition of pollutants on corrosion of different material groups. In most of the industrialized countries decreasing trends of sulphur and nitrogen pollutants and of acidity of precipitation have resulted in decreased corrosion rates. The concept of acceptable levels of pollutants is a useful tool in planning of abatement strategies and for defining of conditions for a suitable development in the field of corrosion of constructions in the atmosphere.

La contaminación de la atmósfera ha sido la principal razón del grave deterioro de las edificaciones y de los monumentos en numerosas ciudades de Europa y Norteamérica. De otro lado, el acelerado incremento de los niveles de contaminación en los países menos desarrollados está poniendo en peligro la estabilidad de los materiales utilizados. Además del importante papel que en este sentido juega el SO₂, la acción directa o el efecto sinérgico de los NO_x y el O₃, al igual que el material particulado y las lluvias acidas contribuyen a agravar el problema. Resultados de vastos programas internacionales de investigación como, por ejemplo, el UN/ECE, han permitido desarrollar relaciones dosis-respuesta que describen el efecto de la deposición de los contaminantes sobre la corrosión de

Water side corrosion prevention in boilers

International Nuclear Information System (INIS)

Zeid, A.

1993-01-01

Corrosion may be defined as a naturally occurring physical and chemical deterioration of a material due to reaction with the environment or surrounding atmosphere. In boilers the material is subjected on both sides to two different media which may cause severe corrosion. At the water side the content of O 2 considered one of the principal factors which determine the extent of corrosion in the boiler tubes. This paper deals with certain conditions that result in the increase of O 2 in the boiler water and hence increase the corrosion rate, to minimize the effect of these conditions a chemical treatment was carried out the results obtained indicated the success of the treatment procedure in corrosion prevention and boiler material protection. The treatment is traditional. But the study indicates how a simple mean could be applied to solve a serious problem. 4 tab

Effect of corrosion product layer on SCC susceptibility of copper containing type 304 stainless steel in 1 M H2SO4

International Nuclear Information System (INIS)

Asawa, M.; Devasenapathi, A.; Fujisawa, M.

2004-01-01

The effect of surface corrosion product layer on the stress corrosion cracking (SCC) susceptibility of type 304 stainless steel with Cu was studied in 1 kmol/m 3 (1 M) sulfuric acid at 353 K temperature. Studies based on the intermittent removal of surface corrosion product layer indicated that the surface film governs the SCC behavior of the alloy by accelerating both the crack initiation and propagation stages. The electrochemical impedance and polarization studies showed the surface layer to be promoting SCC initiation by lowering the uniform corrosion rate and the propagation by shifting the surface corrosion potential to a more noble direction. The elemental analysis of the corrosion product both by the energy dispersive X-ray (EDX) spectroscopy and by X-ray diffraction (XRD) analysis along with the thermodynamic calculations showed the layer to be constituted mainly of metallic copper (Cu) and the mono-hydrated iron sulfate which acts as cathode promoting SCC

Effectiveness of using pure copper and silver coupon corrosivity monitoring (CCM) metal strips to measure the severity levels of air pollutants in indoor and outdoor atmospheres

CSIR Research Space (South Africa)

Foax, LJ

2008-10-01

Full Text Available Severity levels of air pollutants rich in oxides, chlorides and sulphides were successfully measured in indoor and outdoor atmospheres using pure copper and silver coupon corrosivity monitoring (CCM) metal strips when the maximum exposure periods...

The mechanisms underlying corrosion product formation and deposition in nuclear power plant circuits through the action of galvanic and thermal electromotive forces

International Nuclear Information System (INIS)

Brusakov, V.P.; Sedov, V.M.; Khitrov, Yu.A.; Brusov, K.N.; Razmashkin, N.V.; Versin, V.V.; Rybalchenko, I.L.

1983-01-01

From a theoretical standpoint, the processes of formation of corrosion products in nuclear power plant circuits, deposition of corrosion products on the circuit surfaces, formation of an equilibrium concentration of corrosion products in the coolant, and distribution of radionuclides resulting from corrosion in different parts of the circuit are considered. It is shown that the main driving forces for the mass-transfer processes in the circuits are the thermal and galvanic electromotive forces (EMF) of the microcouples. On the basis of the theoretical concepts developed the authors have obtained analytical dependences for calculating the individual stages of the process of corrosion product transfer in the circuits. The mechanisms underlying the processes which occur as a result of thermal and galvanic EMFs are considered, together with the factors influencing these processes. The results of verification of the dependences by computational methods are given and they are compared with operational data from nuclear and conventional thermal power plants and with experimental data. (author)

Electrochemical Characterisation of Filiform Corrosion on Aluminium Rolled Products

NARCIS (Netherlands)

Huisert, M.

2001-01-01

When aluminium is protected by an organic coating a special form of corrosion can occur underneath the organic coating; filiform corrosion. This form of corrosion manifests itself as threadlike filaments under the coating, it causes local delamination of the coating and the coating cannot protect

Electrochemical noise evaluation of anodized aluminum. Comparative study against corrosion behaviour in the atmosphere

Directory of Open Access Journals (Sweden)

Betancourt, N.

2003-12-01

Full Text Available The present work reports the evaluation of aluminum and anodized aluminum by electrochemical noise, as a part of the PATINA/CYTED project of the working group Nº 5. A visual examination is also made. The samples were exposed at several Ibero-American atmospheres up to 2 years of exposure. Different thickness of anodized aluminum were evaluated. The electrochemical potential noise of the 5 μm unexposed sample (pattern showed a different behaviour to that showed by the other anodized specimens. This could be due to a slower sealed of the samples of higher thickness. The same behaviour was observed on the samples exposed at the rural station El Pardo. According to the visual examination, the samples of bare aluminum and those of anodized 5 μm thickness were the most affected by pitting corrosion in the highly polluted atmospheres. A good correlation between corrosion behaviour determined by visual examination and EN was obtained.

Como parte de las investigaciones de la Red PATINA el grupo de trabajo Nº 5 dedicó su atención al comportamiento del aluminio desnudo y anodizado con diferentes espesores en diferentes atmósferas de Iberoamérica. En el presente trabajo se presenta una evaluación de patrones de aluminio 99,5 % de pureza desnudo y anodizado con espesores de 15 y 25 μm, mediante ruido electroquímico. Los resultados obtenidos se comparan con el comportamiento determinado en diferentes atmósferas durante un período de 2 años. El ruido de voltaje del patrón de 5 μm de espesor presenta un comportamiento diferente al de los restantes espesores, lo que coincide con una mayor susceptibilidad a la corrosión picadura de este primer anodizado. Se reportan también algunas diferencias en el ruido de corriente. Se concluye que mediante la utilización del ruido electroquímico es posible caracterizar el aluminio con respecto a su sensibilidad a la corrosión picadura en condiciones atmosféricas.

Risk based inspection for atmospheric storage tank

Science.gov (United States)

Nugroho, Agus; Haryadi, Gunawan Dwi; Ismail, Rifky; Kim, Seon Jin

2016-04-01

Corrosion is an attack that occurs on a metallic material as a result of environment's reaction.Thus, it causes atmospheric storage tank's leakage, material loss, environmental pollution, equipment failure and affects the age of process equipment then finally financial damage. Corrosion risk measurement becomesa vital part of Asset Management at the plant for operating any aging asset.This paper provides six case studies dealing with high speed diesel atmospheric storage tank parts at a power plant. A summary of the basic principles and procedures of corrosion risk analysis and RBI applicable to the Process Industries were discussed prior to the study. Semi quantitative method based onAPI 58I Base-Resource Document was employed. The risk associated with corrosion on the equipment in terms of its likelihood and its consequences were discussed. The corrosion risk analysis outcome used to formulate Risk Based Inspection (RBI) method that should be a part of the atmospheric storage tank operation at the plant. RBI gives more concern to inspection resources which are mostly on `High Risk' and `Medium Risk' criteria and less on `Low Risk' shell. Risk categories of the evaluated equipment were illustrated through case study analysis outcome.

Hot corrosion behavior of magnesia-stabilized ceramic material in a lithium molten salt

Energy Technology Data Exchange (ETDEWEB)

Cho, Soo-Haeng, E-mail: nshcho1@kaeri.re.kr [Korea Atomic Energy Research Institute, Daejeon 305-353 (Korea, Republic of); Kim, Sung-Wook [Korea Atomic Energy Research Institute, Daejeon 305-353 (Korea, Republic of); Kim, Dae-Young [Graduate School of Energy Science and Technology, Chungnam National University, Daejeon 305-764 (Korea, Republic of); Lee, Jong-Hyeon, E-mail: jonglee@cnu.ac.kr [Graduate School of Energy Science and Technology, Chungnam National University, Daejeon 305-764 (Korea, Republic of); Graduate School of Advanced Materials Engineering, Chungnam National University, Daejeon 305-764 (Korea, Republic of); Rapidly Solidified Materials Research Center, Chungnam National University, Daejeon 305-764 (Korea, Republic of); Hur, Jin-Mok [Korea Atomic Energy Research Institute, Daejeon 305-353 (Korea, Republic of)

2017-07-15

The isothermal and cyclic corrosion behaviors of magnesia-stabilized zirconia in a LiCl-Li{sub 2}O molten salt were investigated at 650 °C in an argon atmosphere. The weights of as-received and corroded specimens were measured and the microstructures, morphologies, and chemical compositions were analyzed by scanning electron microscopy, X-ray energy dispersive spectroscopy, and X-ray diffraction. For processes where Li is formed at the cathode during electrolysis, the corrosion rate was about five times higher than those of isothermal and thermal cycling processes. During isothermal tests, the corrosion product Li{sub 2}ZrO{sub 3} was formed after 216 h. During thermal cycling, Li{sub 2}ZrO{sub 3} was not detected until after the completion of 14 cycles. There was no evidence of cracks, pores, or spallation on the corroded surfaces, except when Li was formed. We demonstrate that magnesia-stabilized zirconia is beneficial for increasing the hot corrosion resistance of structural materials subjected to high temperature molten salts containing Li{sub 2}O. - Highlights: •Corrosion mechanism of MSZin LiCl-Li{sub 2}O molten salt is proposed. •Formation of Li{sub 2}ZrO{sub 3}is main corrosion mechanism. •There were no cracks, pores and spallation after corrosion test. •MSZ shows high corrosion resistance to LiCl-Li{sub 2}O molten salt.

Influence of Element Substitution on Corrosion Behavior of Bi2Te3-Based Compounds

Science.gov (United States)

Kohri, Hitoshi; Yagasaki, Takayoshi

2018-02-01

Atmospheric water may condense on the surface of Bi2Te3-based compounds constituting the Peltier module, depending on the operating environment used. In the stage of disposal, Bi2Te3-based compounds may come into contact with water in waste disposal sites. There are very few publications about the influence of condensed water on Peltier modules. Bi2Te3-Sb2Te3 or Bi2Te3-Bi2Se3 pseudo binary system compounds are used as p-type material or n-type material, respectively. The lattice distortion will be induced in the crystal of Bi2Te3-based compounds by element substitution due to the reduction in their thermal conductivity. However, the influence of element substitution on the corrosion behavior of Bi2Te3-based compounds remains unclear. In this study, the influence of element substitution on the corrosion behavior of Bi2Te3-based compounds with practical compositions has been investigated. Bi0.5Sb1.5Te3 or Bi2Te2.85Se0.15 was prepared by the vertical Bridgman method. The electrochemical properties at room temperature were evaluated by cyclic voltammetry in a standard three-electrode cell. The working electrolyte was a naturally aerated 0.6 or 3.0 mass% NaCl solution. From the tendency for corrosion potential for all the samples, the corrosion sensitivity of ternary compounds was slightly higher than that of binary compounds. From the trend of current density, it was found that Bi0.5Sb1.5Te3 had a corrosion resistance intermediate between Bi2Te3 and Sb2Te3. On the other hand, corrosion resistance was affected despite a small amount of Se substitution, and the corrosion resistance of Bi2Te2.85Se0.15 was close to or lower than that of Bi2Se3. From the observation results of the corrosion products, the trends of morphology and composition of corrosion products for Bi0.5Sb1.5Te3 or Bi2Te2.85Se0.15 were consistent with those of Sb2Te3 or Bi2Se3, respectively. From the results of x-ray photoelectron spectroscopy for the electrolyte after testing, the possibility that a

Influence of Element Substitution on Corrosion Behavior of Bi2Te3-Based Compounds

Science.gov (United States)

Kohri, Hitoshi; Yagasaki, Takayoshi

2018-06-01

Atmospheric water may condense on the surface of Bi2Te3-based compounds constituting the Peltier module, depending on the operating environment used. In the stage of disposal, Bi2Te3-based compounds may come into contact with water in waste disposal sites. There are very few publications about the influence of condensed water on Peltier modules. Bi2Te3-Sb2Te3 or Bi2Te3-Bi2Se3 pseudo binary system compounds are used as p-type material or n-type material, respectively. The lattice distortion will be induced in the crystal of Bi2Te3-based compounds by element substitution due to the reduction in their thermal conductivity. However, the influence of element substitution on the corrosion behavior of Bi2Te3-based compounds remains unclear. In this study, the influence of element substitution on the corrosion behavior of Bi2Te3-based compounds with practical compositions has been investigated. Bi0.5Sb1.5Te3 or Bi2Te2.85Se0.15 was prepared by the vertical Bridgman method. The electrochemical properties at room temperature were evaluated by cyclic voltammetry in a standard three-electrode cell. The working electrolyte was a naturally aerated 0.6 or 3.0 mass% NaCl solution. From the tendency for corrosion potential for all the samples, the corrosion sensitivity of ternary compounds was slightly higher than that of binary compounds. From the trend of current density, it was found that Bi0.5Sb1.5Te3 had a corrosion resistance intermediate between Bi2Te3 and Sb2Te3. On the other hand, corrosion resistance was affected despite a small amount of Se substitution, and the corrosion resistance of Bi2Te2.85Se0.15 was close to or lower than that of Bi2Se3. From the observation results of the corrosion products, the trends of morphology and composition of corrosion products for Bi0.5Sb1.5Te3 or Bi2Te2.85Se0.15 were consistent with those of Sb2Te3 or Bi2Se3, respectively. From the results of x-ray photoelectron spectroscopy for the electrolyte after testing, the possibility that a

Accelerated atmospheric corrosion testing using a cyclic wet/dry exposure test

International Nuclear Information System (INIS)

Lyon, S.B.; Thompson, G.E.; Johnson, J.E.; Wood, G.C.

1989-01-01

Aluminum corrosion is important in overhead electrical conductors constructed from aluminum wire centrally reinforced by galvanized steel strands. Inspection of conductor after long service has implicated rubber bushing material, on the outside, and the galvanized strands, on the inside, as providing potential galvanic sites for the initiation of rapid aluminum corrosion. Therefore, the galvanic corrosion of aluminum in contact with graphite-loaded neoprene rubber, hot-dip galvanized steel and steel was assessed in a cyclic wet/dry exposure test using mixed-salts spray solutions containing appropriate ratios of sulfate and chloride ion. Aluminum was found to corrode at between 3 to 6 times its uncoupled rate when associated with the rubber material. While the eta-phase, relatively pure Zn, galvanized layer remained intact, galvanic corrosion of aluminum was slow. However, on exposure of the zeta-phase, Zn/Fe intermetallic layer, aluminum corroded about 35 times faster than expected in a solution with a high level of Cl - ion. The importance of these data to conductor lifetime is discussed

On the mechanisms of the corrosion of weathering steel by SO{sub 2} in laboratory studies: influence of the environmental parameters

Energy Technology Data Exchange (ETDEWEB)

Marco, J. F., E-mail: jfmarco@iqfr.csic.es [Instituto de Química Física “Rocasolano”, CSIC (Spain)

2017-11-15

We report here on the mechanisms underlying the corrosion of weathering steel in accelerated laboratory tests using artificially polluted SO{sub 2}-atmospheres. The role of corrosion parameters such as the SO{sub 2} concentration, the exposure time, the relative humidity and temperature of the environment are discussed in detail. Through the extensive use of Mössbauer spectroscopy in both its transmission and electron detection modes, as well as with the help of other analysis techniques, the characterization of the different corrosion products at the various stages of the corrosion process has been carried out. The results complement the data obtained in field studies and help to understand the mechanisms involved in this complex phenomenon.

Application Of Fractal Dimension On Atmospheric Corrosion Of Galvanized Iron Roofing Material

OpenAIRE

Issa A.K; Abba. M. Aji

2015-01-01

Abstract Corrosion rates of galvanized iron roofing sheet In yola north eastern part of Nigeria were assessed and determined by weight loss method and scanner fractal analysis method. Scanning electronic machine SEM was used to transform corrosion coupons to electronic form for image j processing and analysing software The result of corrosion rates for these two methods after six months of the samples exposure in industrial. Coastal market and urban areas in the region are 1.51 1.079 1.051 0....

Corrosion and protection of metals in the rural atmosphere of "El Pardo" Spain (PATINA / CYTED project

Directory of Open Access Journals (Sweden)

Simancas, J.

2003-12-01

Full Text Available Atmospheric corrosion tests of metallic and organic coatings on steel, zinc and aluminium have been conducted in "El Pardo" (Spain as part of the PATINA/CYTED project "Anticorrosive Protection of Metals in the Atmosphere". This is a rural atmosphere with the following ISO corrosivity categories: C2 (Fe, C2 (Zn, C3 (Cu and Cl (Al. Its average temperature and relative humidity is 13 °C and 62.8 %, respectively, and it has low SO₂ and Cl^- contents. Results of 42 months exposure are discussed. Atmospheric exposure tests were carried out for the following types of coatings: conventional paint coatings for steel and hot-dip galvanized steel (group 1, new painting technologies for steel and galvanized steel (group 2, zinc-base metallic coatings (group 3, aluminium-base metallic coatings (group 4, coatings on aluminium (group 5 and coil-coatings on steel, hot-dip galvanized steel and 55 % Al-Zn coated steel (group 6.

Como parte del proyecto PATINA/CYTED "Protección anticorrosiva de metales en la atmósfera" se han llevado a cabo en la estación de ensayo de "El Pardo" (España, ensayos de corrosión atmosférica de recubrimientos metálicos y orgánicos sobre acero, zinc y aluminio. Se trata de una atmósfera rural según la clasificación ISO de grado de corrosividad: C2 (Fe, C2 (Zn, C3 (Cu y Cl (Al. La temperatura y humedad relativa media es de 13 °C y 62,8 %, respectivamente, y tiene bajos contenidos de SO₂ y Cl^-. Se discuten los resultados obtenidos después de 42 meses de exposición. Los ensayos de corrosión atmosférica se llevaron a cabo para tres tipos de recubrimientos: recubrimientos de pintura convencional sobre acero y acero zincado (grupo 1, nuevas tecnologías en pinturas para acero y acero galvanizado (grupo 2, recubrimientos metálicos base zinc (grupo 3, recubrimientos metálicos base aluminio (grupo 4, recubrimientos sobre aluminio (grupo 5 y recubrimientos de banda en continuo

Study of the formation and transport of corrosion products in PWR primary circuit simulators

International Nuclear Information System (INIS)

Noe, M.; Frejaville, G.; Camp, J.J.

1983-01-01

The formation, migration and deposition of corrosion products in PWR primary circuits are studied in out-of-reactor loops. The aim of these studies is to limit the build-up of the radiation fields impinging on out-of-flux walls and to reduce the danger of rapid corrosion of fuel cans, taking into account the tougher conditions imposed on current trends in the operation of such industrial plants. Four simulator loops and their respective possibilities and research methods are described. (author)

Task E container corrosion studies: Annual report. Revision 1

International Nuclear Information System (INIS)

Bunnell, L.R.; Doremus, L.A.; Topping, J.B.; Duncan, D.R.

1994-06-01

The Pacific Northwest Laboratory is conducting the Solid Waste Technology Support Program (SWTSP) for Westinghouse Hanford Company (WHC). Task E is the Container Corrosion Study Portion of the SWTSP that will perform testing to provide defensible data on the corrosion of low-carbon steel, as used in drums to contain chemical and radioactive wastes at the Hanford Site. A second objective of Task E is to provide and test practical alternative materials that have higher corrosion resistance than low-carbon steel. The scope of work for fiscal year (FY) 1993 included initial testing of mild steel specimens buried in Hanford soils or exposed to atmospheric corrosion in metal storage sheds. During FY 1993, progress was made in three areas of Task E. First, exposure of test materials began at the Soil Corrosion Test Site where low-carbon steel specimens were placed in the soil in five test shafts at depths of 9 m (30 ft). Second, the corrosion measurement of low-carbon steel in the soil of two solid waste trenches continued. The total exposure time is ∼ 500 days. Third, an atmospheric corrosion test of low-carbon steel was initiated in a metal shed (Building 2401-W) in the 200 West Area. This annual report describes the Task E efforts and provides a current status

Modeling of Metal Structure Corrosion Damage: A State of the Art Report

Directory of Open Access Journals (Sweden)

Francesco Portioli

2010-07-01

Full Text Available The durability of metal structures is strongly influenced by damage due to atmospheric corrosion, whose control is a key aspect for design and maintenance of both new constructions and historical buildings. Nevertheless, only general provisions are given in European codes to prevent the effects of corrosion during the lifetime of metal structures. In particular, design guidelines such as Eurocode 3 do not provide models for the evaluation of corrosion depth that are able to predict the rate of thickness loss as a function of different influencing parameters. In this paper, the modeling approaches of atmospheric corrosion damage of metal structures, which are available in both ISO standards and the literature, are presented. A comparison among selected degradation models is shown in order to evaluate the possibility of developing a general approach to the evaluation of thickness loss due to corrosion.

A thermogravimetric analyzer for corrosive atmospheres, and its application to the chlorination of ZrO2-C mixtures

International Nuclear Information System (INIS)

Pasquevich, Daniel; Caneiro, Alberto

1990-01-01

A thermogravimetric analyzer built on the basis of a Cahn 2000 electrobalance, suitable for using with corrosive atmospheres, is reported. The corrections for buoyancy and gas-flow effects, which strongly modify the thermogravimetric curves are discussed. As an application, the kinetics of a reaction between chlorine and a mixture of zirconia and carbon has been studied. It has been able to measure the uptake of chlorine by carbon and the reaction rate within the first 50 seconds. Evidence of a transition to quite a different reaction rate at longer times is presented. (Author)