The initial atmospheric corrosion of ZM (ZnAlMg)-coated steel in humid air (85% RH) and humid argon (85% RH) containing 320 ppb SO2 was studied using in situ infrared reflection absorption spectroscopy (IRRAS), FTIR-ATR focal plane array (FPA) imaging and SEM-EDS. The corrosion products formed in humid air containing SO2 are mainly composed of magnesium sulphites and sulphates, with sulphite-containing corrosion products formed initially while the contribution from sulphates increased with exposure time. The results from FTIR-FPA imaging and SEM-EDS showed that the magnesium sulphite and sulphate are formed mainly on eutectic phases with a higher quantity of corrosion products formed on the binary eutectic (Zn-MgZn2) phases. This is due to presence of microgalvanic elements with the zinc-rich phases as the main sites for the cathodic oxygen reduction while the anodic reactions take place on the eutectic areas. Sulphate content is the highest on the binary eutectic phases, due to the microgalvanic effects and the production of oxidants by the cathodic reaction, which increases the oxidation of sulphite to sulphate.
{"title":"The Effect of Microstructure on Local Corrosion Product Formation during Initial SO2-Induced Atmospheric Corrosion of ZnAlMg Coating Studied by FTIR-ATR FPA Chemical Imaging","authors":"Dan Persson, Dominique Thierry, N. LeBozec","doi":"10.3390/cmd4030026","DOIUrl":"https://doi.org/10.3390/cmd4030026","url":null,"abstract":"The initial atmospheric corrosion of ZM (ZnAlMg)-coated steel in humid air (85% RH) and humid argon (85% RH) containing 320 ppb SO2 was studied using in situ infrared reflection absorption spectroscopy (IRRAS), FTIR-ATR focal plane array (FPA) imaging and SEM-EDS. The corrosion products formed in humid air containing SO2 are mainly composed of magnesium sulphites and sulphates, with sulphite-containing corrosion products formed initially while the contribution from sulphates increased with exposure time. The results from FTIR-FPA imaging and SEM-EDS showed that the magnesium sulphite and sulphate are formed mainly on eutectic phases with a higher quantity of corrosion products formed on the binary eutectic (Zn-MgZn2) phases. This is due to presence of microgalvanic elements with the zinc-rich phases as the main sites for the cathodic oxygen reduction while the anodic reactions take place on the eutectic areas. Sulphate content is the highest on the binary eutectic phases, due to the microgalvanic effects and the production of oxidants by the cathodic reaction, which increases the oxidation of sulphite to sulphate.","PeriodicalId":10693,"journal":{"name":"Corrosion and Materials Degradation","volume":"85 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2023-09-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"80477662","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Robert Sottor, Ricarda Gruen, Kerstin Kremmer, S. Lederer, M. Schneider, Wolfram Fuerbeth
Plasma electrolytic oxidation (PEO) in an alkaline silicate electrolyte containing nanosized sepiolite fibers was carried out on magnesium alloy AZ31. The mineral fibers were loaded with different corrosion inhibitors and incorporated in situ during the PEO treatment. The composition and microstructure of the PEO coatings were investigated by SEM. It was shown that the fibers are located on the surface as well as inside the “weak spots” of the coating, i.e., pores and discharge channels. The fixation of the particles is caused by sintering due to the heat developed during the PEO treatment. Investigations using electrochemical impedance spectroscopy and linear sweep voltammetry in 0.01 M NaCl solution confirmed an improvement of the corrosion protection. The use of the inhibitors shifts the critical pitting potential in the anodic direction. Regarding efficiency, cerium-loaded sepiolite showed the best behavior by shifting the pitting potential by +0.9 V.
在含纳米海泡石纤维的碱性硅酸盐电解质中对镁合金AZ31进行了等离子体电解氧化(PEO)。在PEO处理过程中，矿物纤维被装载了不同的缓蚀剂，并在原位掺入。用扫描电镜研究了PEO涂层的组成和微观结构。结果表明，纤维既位于涂层的表面，也位于涂层的“薄弱点”，即孔隙和放电通道内。由于PEO处理过程中产生的热量，颗粒的固定是由烧结引起的。通过电化学阻抗谱和线性扫描伏安法在0.01 M NaCl溶液中的研究，证实了该材料的防腐性能有所提高。抑制剂的使用使临界点蚀电位向阳极方向移动。在效率方面，载铈海泡石表现出最好的行为，将点蚀电位移动了+0.9 V。
{"title":"Plasma Electrolytic Oxidation on Magnesium AZ31 with Sepiolite as Inhibitor Carrier for Improved Corrosion Protection","authors":"Robert Sottor, Ricarda Gruen, Kerstin Kremmer, S. Lederer, M. Schneider, Wolfram Fuerbeth","doi":"10.3390/cmd4030025","DOIUrl":"https://doi.org/10.3390/cmd4030025","url":null,"abstract":"Plasma electrolytic oxidation (PEO) in an alkaline silicate electrolyte containing nanosized sepiolite fibers was carried out on magnesium alloy AZ31. The mineral fibers were loaded with different corrosion inhibitors and incorporated in situ during the PEO treatment. The composition and microstructure of the PEO coatings were investigated by SEM. It was shown that the fibers are located on the surface as well as inside the “weak spots” of the coating, i.e., pores and discharge channels. The fixation of the particles is caused by sintering due to the heat developed during the PEO treatment. Investigations using electrochemical impedance spectroscopy and linear sweep voltammetry in 0.01 M NaCl solution confirmed an improvement of the corrosion protection. The use of the inhibitors shifts the critical pitting potential in the anodic direction. Regarding efficiency, cerium-loaded sepiolite showed the best behavior by shifting the pitting potential by +0.9 V.","PeriodicalId":10693,"journal":{"name":"Corrosion and Materials Degradation","volume":"47 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2023-08-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"80325030","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Since 2011, there has been an international effort to evaluate the behavior of newer fuel rod materials for the retrofitting of existing light water reactors (LWR). These materials include concepts for the cladding of the fuel and for the fuel itself. The materials can be broadly categorized into evolutionary or improved existing materials and revolutionary or innovative materials. The purpose of the newer materials or accident-tolerant fuels (ATF) is to make the LWRs more resistant to loss-of-coolant accidents and thus increase their operation safety. The benefits and detriments of the three main concepts for the cladding are discussed. These include (i) coatings for existing zirconium alloys; (ii) monolithic iron–chromium–aluminum alloys; and (iii) composites based on silicon carbide. The use of ATF materials may help extend the life of currently operating LWRs, while also being a link to material development for future commercial reactors.
{"title":"Improved and Innovative Accident-Tolerant Nuclear Fuel Materials Considered for Retrofitting Light Water Reactors—A Review","authors":"R. B. Rebak","doi":"10.3390/cmd4030024","DOIUrl":"https://doi.org/10.3390/cmd4030024","url":null,"abstract":"Since 2011, there has been an international effort to evaluate the behavior of newer fuel rod materials for the retrofitting of existing light water reactors (LWR). These materials include concepts for the cladding of the fuel and for the fuel itself. The materials can be broadly categorized into evolutionary or improved existing materials and revolutionary or innovative materials. The purpose of the newer materials or accident-tolerant fuels (ATF) is to make the LWRs more resistant to loss-of-coolant accidents and thus increase their operation safety. The benefits and detriments of the three main concepts for the cladding are discussed. These include (i) coatings for existing zirconium alloys; (ii) monolithic iron–chromium–aluminum alloys; and (iii) composites based on silicon carbide. The use of ATF materials may help extend the life of currently operating LWRs, while also being a link to material development for future commercial reactors.","PeriodicalId":10693,"journal":{"name":"Corrosion and Materials Degradation","volume":"59 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2023-08-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"77266059","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
This research article explores the potential of optical fibers as sensors, highlighting their ability to measure various parameters such as temperature, pressure, stress, and radiation dose. The study focuses on investigating the material compatibility of optical fibers in challenging sensing environments like Gen II/II+ and advance nuclear reactors, as well as concentrated solar power (CSP) plants. Material compatibility tests were conducted to determine the feasibility of using fluorine and germanium optical fiber sensors in these environments. The study found that raw fibers were corrosion-resistant to lead bismuth eutectic at 600 °C, regardless of the coating. In molten salt environments, raw fibers were incompatible with FLiNaK but showed corrosion resistance to MgCl₂-NaCl-KCl. However, the survivability of raw fiber optics improved with a gold coating in FLiNaK. Raw fiber optics were found to be incompatible in high-temperature steam at 1200 °C and in a pressurized water reactor (PWR) at 300 °C.
{"title":"Corrosion of Silica-Based Optical Fibers in Various Environments","authors":"Amanda Leong, S. Rountree, Jinsuo Zhang","doi":"10.3390/cmd4030023","DOIUrl":"https://doi.org/10.3390/cmd4030023","url":null,"abstract":"This research article explores the potential of optical fibers as sensors, highlighting their ability to measure various parameters such as temperature, pressure, stress, and radiation dose. The study focuses on investigating the material compatibility of optical fibers in challenging sensing environments like Gen II/II+ and advance nuclear reactors, as well as concentrated solar power (CSP) plants. Material compatibility tests were conducted to determine the feasibility of using fluorine and germanium optical fiber sensors in these environments. The study found that raw fibers were corrosion-resistant to lead bismuth eutectic at 600 °C, regardless of the coating. In molten salt environments, raw fibers were incompatible with FLiNaK but showed corrosion resistance to MgCl₂-NaCl-KCl. However, the survivability of raw fiber optics improved with a gold coating in FLiNaK. Raw fiber optics were found to be incompatible in high-temperature steam at 1200 °C and in a pressurized water reactor (PWR) at 300 °C.","PeriodicalId":10693,"journal":{"name":"Corrosion and Materials Degradation","volume":"16 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2023-08-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"84350040","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
The alkali–aggregate reactivity (AAR) of concrete, long known for mass concrete, can also induce corrosion of steel in reinforced concrete structures. Several examples are given for which the origin of observed reinforcement corrosion and loss of concrete cover originally was attributed to chloride-induced or to carbonation-induced reinforcement corrosion. Critical reviews of these cases, using available information, suggest that, more likely, the observed crack patterns and concrete deterioration are the result of long-term AAR-induced concrete matrix expansion and loss of concrete strength and that these effects occurred prior to the eventual initiation of reinforcement corrosion. This proposition is supported by finite element and other stress analyses of various concrete–steel ensembles. They show that concrete expansion produces tensile stresses localised at and near exterior concrete surfaces or relative to the reinforcement. The locations of high-stress and -strain zones so produced correlate with field observations of long-term concrete cracking and delamination. The present interpretations highlight that AAR may be a significant contributor to initiation and subsequent long-term development of reinforcement corrosion in structurally reinforced concretes.
{"title":"Concrete Alkali–Aggregate-Reactivity-Induced Steel Reinforcement Corrosion","authors":"R. Melchers, Henry Humphrey","doi":"10.3390/cmd4030022","DOIUrl":"https://doi.org/10.3390/cmd4030022","url":null,"abstract":"The alkali–aggregate reactivity (AAR) of concrete, long known for mass concrete, can also induce corrosion of steel in reinforced concrete structures. Several examples are given for which the origin of observed reinforcement corrosion and loss of concrete cover originally was attributed to chloride-induced or to carbonation-induced reinforcement corrosion. Critical reviews of these cases, using available information, suggest that, more likely, the observed crack patterns and concrete deterioration are the result of long-term AAR-induced concrete matrix expansion and loss of concrete strength and that these effects occurred prior to the eventual initiation of reinforcement corrosion. This proposition is supported by finite element and other stress analyses of various concrete–steel ensembles. They show that concrete expansion produces tensile stresses localised at and near exterior concrete surfaces or relative to the reinforcement. The locations of high-stress and -strain zones so produced correlate with field observations of long-term concrete cracking and delamination. The present interpretations highlight that AAR may be a significant contributor to initiation and subsequent long-term development of reinforcement corrosion in structurally reinforced concretes.","PeriodicalId":10693,"journal":{"name":"Corrosion and Materials Degradation","volume":"68 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2023-07-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"90239723","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
The destruction of the passive oxide can be caused by the action of a radionuclide, which collides with the surface of the oxide. In this case, the β− nuclear particle produced by the decay of tritiated water is considered for corrosion, and it follows that the β− energy is absorbed first into the oxide. The penetration depth is sufficient for all the passive oxides to be destabilized. Destabilization was examined by voltammetry and by the electrochemical circuit in the passive potential. The corresponding pathway leads to the destruction of oxide. Tests carried out using a chaos data analyzer are an aid for expertise. Different behavior may occur depending on the passive potential and the β− density. The synchronization of phase space spectra and tests realized sector by sector make possible the interpretation of divergence leading to unstable oxide and oxide destruction at different passive potentials and for different β− particle densities.
{"title":"Passive Oxide Destruction by Dense Low-Energy Radionuclide i-Analyzed by Voltammetry ii-Analyzed by Chaos","authors":"G. Bellanger","doi":"10.3390/cmd4030021","DOIUrl":"https://doi.org/10.3390/cmd4030021","url":null,"abstract":"The destruction of the passive oxide can be caused by the action of a radionuclide, which collides with the surface of the oxide. In this case, the β− nuclear particle produced by the decay of tritiated water is considered for corrosion, and it follows that the β− energy is absorbed first into the oxide. The penetration depth is sufficient for all the passive oxides to be destabilized. Destabilization was examined by voltammetry and by the electrochemical circuit in the passive potential. The corresponding pathway leads to the destruction of oxide. Tests carried out using a chaos data analyzer are an aid for expertise. Different behavior may occur depending on the passive potential and the β− density. The synchronization of phase space spectra and tests realized sector by sector make possible the interpretation of divergence leading to unstable oxide and oxide destruction at different passive potentials and for different β− particle densities.","PeriodicalId":10693,"journal":{"name":"Corrosion and Materials Degradation","volume":"72 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2023-07-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"78649383","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Lina E. Dominici, K. Duncan, M. Nanny, I. Davidova, Brian H. Harriman, J. M. Suflita
The biocorrosion of carbon steel poses a risk for ships combining seawater and fuel in metal ballast tanks. Ballast tanks were simulated by duplicate reactors containing carbon steel coupons and either petroleum F76 (petro-F76), Fischer–Tropsch F76 (FT-F76), or a 1:1 mix of both fuels, to investigate whether the alternative fuel FT-F76 influenced this risk. The polycarbonate reactors were inoculated with seawater, and the control reactors did not receive fuel. The reactors were monitored for 400 days, and they all reached a pH and open circuit potential where elemental iron was oxidized, indicating corrosion. The reactors containing petro-76 or fuel mix had higher levels of dissolved iron; one of each replicate had lower concentrations of sulfate than the original seawater, while the sulfate concentration did not decrease in the other incubations. The high sulfate reactors, but not the low sulfate reactors, had a high relative abundance of microaerophilic sulfide-oxidizing bacteria. The FT-F76 and the no-fuel reactors had a high relative abundance of iron-sequestering Magnetovibrio. Although dissolved iron and loss of sulfate under anoxic conditions are associated with biocorrosion, our results suggest that in our reactors these indicators were altered by iron-sequestering and sulfide-oxidizing microbes, which is consistent with the slow diffusion of oxygen across the polycarbonate reactors.
{"title":"Microbial Communities Associated with Alternative Fuels in Model Seawater-Compensated Fuel Ballast Tanks","authors":"Lina E. Dominici, K. Duncan, M. Nanny, I. Davidova, Brian H. Harriman, J. M. Suflita","doi":"10.3390/cmd4030020","DOIUrl":"https://doi.org/10.3390/cmd4030020","url":null,"abstract":"The biocorrosion of carbon steel poses a risk for ships combining seawater and fuel in metal ballast tanks. Ballast tanks were simulated by duplicate reactors containing carbon steel coupons and either petroleum F76 (petro-F76), Fischer–Tropsch F76 (FT-F76), or a 1:1 mix of both fuels, to investigate whether the alternative fuel FT-F76 influenced this risk. The polycarbonate reactors were inoculated with seawater, and the control reactors did not receive fuel. The reactors were monitored for 400 days, and they all reached a pH and open circuit potential where elemental iron was oxidized, indicating corrosion. The reactors containing petro-76 or fuel mix had higher levels of dissolved iron; one of each replicate had lower concentrations of sulfate than the original seawater, while the sulfate concentration did not decrease in the other incubations. The high sulfate reactors, but not the low sulfate reactors, had a high relative abundance of microaerophilic sulfide-oxidizing bacteria. The FT-F76 and the no-fuel reactors had a high relative abundance of iron-sequestering Magnetovibrio. Although dissolved iron and loss of sulfate under anoxic conditions are associated with biocorrosion, our results suggest that in our reactors these indicators were altered by iron-sequestering and sulfide-oxidizing microbes, which is consistent with the slow diffusion of oxygen across the polycarbonate reactors.","PeriodicalId":10693,"journal":{"name":"Corrosion and Materials Degradation","volume":"181 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2023-07-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"74382380","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Saleh Ahmed, Yang Hou, K. Lepkova, T. Pojtanabuntoeng
This paper investigated carbon steel corrosion in an enclosed environment, where one set of steel was immersed in 3.5 wt.% NaCl solution and another exposed to humid (condensation) conditions. The study employed electrochemical noise and electrochemical impedance spectroscopy techniques to monitor real time corrosion behaviour. The samples were evaluated with surface characterisation techniques including optical light microscope, scanning electron microscope with energy dispersive X-ray spectroscopy, and Raman spectroscopy. The results showed that carbon steel immersed in the liquid phase at a constant temperature exhibited the highest weight loss. However, the carbon steel exposed to water condensation (gas phase) at 80 °C manifested extensive localised corrosion. EN results agreed with the microscopy findings.
{"title":"Investigation of the Effect Chloride Ions on Carbon Steel in Closed Environments at Different Temperatures","authors":"Saleh Ahmed, Yang Hou, K. Lepkova, T. Pojtanabuntoeng","doi":"10.3390/cmd4030019","DOIUrl":"https://doi.org/10.3390/cmd4030019","url":null,"abstract":"This paper investigated carbon steel corrosion in an enclosed environment, where one set of steel was immersed in 3.5 wt.% NaCl solution and another exposed to humid (condensation) conditions. The study employed electrochemical noise and electrochemical impedance spectroscopy techniques to monitor real time corrosion behaviour. The samples were evaluated with surface characterisation techniques including optical light microscope, scanning electron microscope with energy dispersive X-ray spectroscopy, and Raman spectroscopy. The results showed that carbon steel immersed in the liquid phase at a constant temperature exhibited the highest weight loss. However, the carbon steel exposed to water condensation (gas phase) at 80 °C manifested extensive localised corrosion. EN results agreed with the microscopy findings.","PeriodicalId":10693,"journal":{"name":"Corrosion and Materials Degradation","volume":"85 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2023-06-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"84059879","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pascual Saura Gómez, Javier Sánchez Montero, J. E. Torres Martín, S. Chinchón-Payá, N. Rebolledo Ramos, Óscar Galao Malo
Most regulations on the manufacturing of concrete for reinforced concrete structures rest on durability models that consider the corrosion of reinforcements. Those models are based on factors such as humidity, frost, presence of chlorides, and internal characteristics of the concrete itself, like resistance, porosity, type of cement, water/cement ratio, etc. No regulations, however, adopt a purely constructive perspective when evaluating the risk of corrosion, i.e., the relative position of the reinforced concrete in buildings. The present work focuses on the relationship between the position of the damaged element and the building envelope. A total of 84 elements (columns and reinforced concrete beams) across twenty buildings were analysed in the provinces of Alicante and Murcia (Spain). The reinforcement concrete of these elements underwent carbonation-induced corrosion according to their positions in the buildings: (A) façade columns in contact with the ground; (B) interior columns in contact with the ground; (C) columns of walls in contact with the ground; (D) columns and external beams protected from rain; (E) columns and external beams exposed to rain; (F) columns and beams in air chambers under sanitary slabs; and (G), columns and interior beams. Of all types, elements (E) and (F) suffered carbonation-induced corrosion faster than the models used in the regulations, and type (G) underwent slower carbonation.
{"title":"Carbonation-Induced Corrosion of Reinforced Concrete Elements according to Their Positions in the Buildings","authors":"Pascual Saura Gómez, Javier Sánchez Montero, J. E. Torres Martín, S. Chinchón-Payá, N. Rebolledo Ramos, Óscar Galao Malo","doi":"10.3390/cmd4030018","DOIUrl":"https://doi.org/10.3390/cmd4030018","url":null,"abstract":"Most regulations on the manufacturing of concrete for reinforced concrete structures rest on durability models that consider the corrosion of reinforcements. Those models are based on factors such as humidity, frost, presence of chlorides, and internal characteristics of the concrete itself, like resistance, porosity, type of cement, water/cement ratio, etc. No regulations, however, adopt a purely constructive perspective when evaluating the risk of corrosion, i.e., the relative position of the reinforced concrete in buildings. The present work focuses on the relationship between the position of the damaged element and the building envelope. A total of 84 elements (columns and reinforced concrete beams) across twenty buildings were analysed in the provinces of Alicante and Murcia (Spain). The reinforcement concrete of these elements underwent carbonation-induced corrosion according to their positions in the buildings: (A) façade columns in contact with the ground; (B) interior columns in contact with the ground; (C) columns of walls in contact with the ground; (D) columns and external beams protected from rain; (E) columns and external beams exposed to rain; (F) columns and beams in air chambers under sanitary slabs; and (G), columns and interior beams. Of all types, elements (E) and (F) suffered carbonation-induced corrosion faster than the models used in the regulations, and type (G) underwent slower carbonation.","PeriodicalId":10693,"journal":{"name":"Corrosion and Materials Degradation","volume":"48 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2023-06-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"73189602","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
F. Queiroz, Aline de Fátima Santos Bugarin, Victor H. Ayusso, M. Terada, I. Costa
The AA 2198-T851 is a third-generation Al-Li alloy developed for use in the aircraft industry. Al-Li alloys are susceptible to localized corrosion due to their complex microstructure resulting from the used thermomechanical treatment. In order to prevent localized corrosion, these alloys are usually protected by anodizing in order to avoid a corrosive environment. Subsequently, for anodizing, a sealing treatment is usually performed for parts. Some sealing treatments use hexavalent-chromium-ion-containing solutions. In this investigation, a chromium-free sealing treatment in a solution with cerium ions has been carried out, and the effect on the corrosion resistance of the AA2198-T851 alloy was investigated. Hydrothermally sealed or unsealed samples were also tested for corrosion resistance for comparison reasons. The corrosion resistance of the anodized aluminum alloy, either hydrothermally sealed or in a cerium-ion-containing solution, was evaluated in a sodium chloride solution by electrochemical impedance spectroscopy as a function of immersion time. The samples sealed in a cerium-containing solution increased their corrosion resistance when compared to the hydrothermally sealed. The effectiveness of the sealing process with cerium that was observed in the electrochemical tests indicated that after the corrosive attack of the barrier layer, there was a “sealing” process of the sample surface.
AA 2198-T851是为飞机工业开发的第三代铝锂合金。铝锂合金在热处理过程中组织复杂，易发生局部腐蚀。为了防止局部腐蚀，这些合金通常通过阳极氧化来保护，以避免腐蚀环境。随后，对于阳极氧化，通常对零件进行密封处理。有些密封处理使用含六价铬离子的溶液。研究了在含铈离子溶液中进行无铬密封处理对AA2198-T851合金耐腐蚀性能的影响。为了比较，还对水热密封或未密封的样品进行了耐腐蚀性测试。在氯化钠溶液中，用电化学阻抗谱法评价了水热密封和含铈溶液中阳极氧化铝合金的耐蚀性。与水热密封相比，密封在含铈溶液中的样品提高了其耐腐蚀性。电化学试验中观察到的铈密封过程的有效性表明，在阻挡层腐蚀后，样品表面发生了“密封”过程。
{"title":"Investigation on the Effect of a Chromium-Free Sealing Treatment for the Corrosion Resistance of AA2198-T851 after Tartaric Sulphuric Anodizing (TSA)","authors":"F. Queiroz, Aline de Fátima Santos Bugarin, Victor H. Ayusso, M. Terada, I. Costa","doi":"10.3390/cmd4020017","DOIUrl":"https://doi.org/10.3390/cmd4020017","url":null,"abstract":"The AA 2198-T851 is a third-generation Al-Li alloy developed for use in the aircraft industry. Al-Li alloys are susceptible to localized corrosion due to their complex microstructure resulting from the used thermomechanical treatment. In order to prevent localized corrosion, these alloys are usually protected by anodizing in order to avoid a corrosive environment. Subsequently, for anodizing, a sealing treatment is usually performed for parts. Some sealing treatments use hexavalent-chromium-ion-containing solutions. In this investigation, a chromium-free sealing treatment in a solution with cerium ions has been carried out, and the effect on the corrosion resistance of the AA2198-T851 alloy was investigated. Hydrothermally sealed or unsealed samples were also tested for corrosion resistance for comparison reasons. The corrosion resistance of the anodized aluminum alloy, either hydrothermally sealed or in a cerium-ion-containing solution, was evaluated in a sodium chloride solution by electrochemical impedance spectroscopy as a function of immersion time. The samples sealed in a cerium-containing solution increased their corrosion resistance when compared to the hydrothermally sealed. The effectiveness of the sealing process with cerium that was observed in the electrochemical tests indicated that after the corrosive attack of the barrier layer, there was a “sealing” process of the sample surface.","PeriodicalId":10693,"journal":{"name":"Corrosion and Materials Degradation","volume":"27 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2023-06-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"83986791","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
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