Editor’s Choice Articles

In this paper, time/frequency domain data processing was proposed to analyse the EN signal recorded during stress corrosion cracking on precipitation-hardening martensitic stainless steel in a chloride environment. Continuous Wavelet Transform, albeit with some limitations, showed a suitable support in the discriminatory capacity among transient signals related to the different stress corrosion cracking mechanisms. In particular, the aim is to propose the analysis of electrochemical noise signals under stress corrosion cracking conditions in the time–frequency domain by using the Hilbert–Huang approach. The Hilbert–Huang Transform (performed by the Empirical Mode Decomposition approach) was finally proposed to carry out an identification of the corrosion mechanisms in comparison to conventional data processing methods. By using this approach, a detailed simultaneous decomposition of the original electrochemical noise data in the time and frequency domain was carried out. The method gave useful information about transitions among different corrosion mechanisms, allowing us to (i) identify a specific characteristic response for each corrosion damaging phenomenon induced by stress corrosion cracking, (ii) time each corrosion of the damaging phenomenon, and (iii) provide a topological description of the advancing SCC damaging stages. This characteristic evidences that the Hilbert–Huang Transform is a very powerful technique to potentially recognize and distinguish the different corrosion mechanisms occurring during stress corrosion cracking. Full article

Tribocorrosion, a research field that has been evolving for decades, has gained renewed attention in recent years, driven by increased demand for wear- and corrosion-resistant materials from biomedical implants, nuclear power generation, advanced manufacturing, batteries, marine and offshore industries, etc. In the United States, wear and corrosion are estimated to cost nearly USD 300 billion per year. Among various important structural materials, passive metals such as aluminum alloys are most vulnerable to tribocorrosion due to the wear-accelerated corrosion as a result of passive film removal. Thus, designing aluminum alloys with better tribocorrosion performance is of both scientific and practical importance. This article reviews five decades of research on the tribocorrosion of aluminum alloys, from experimental to computational studies. Special focus is placed on two aspects: (1) The effects of alloying and grain size on the fundamental wear, corrosion, and tribocorrosion mechanisms; and (2) Alloy design strategies to improve the tribocorrosion resistance of aluminum alloys. Finally, the paper sheds light on the current challenges faced and outlines a few future research directions in the field of tribocorrosion of aluminum alloys. Full article

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. Full article

Polymer-based coatings are a long-established category of protective coatings for metals and alloys regarding corrosion inhibition. The polymer films can degrade, and when coated on metallic substrates, the degradation facilitates moisture and oxygen penetration, reducing the polymer film’s adhesion to the metallic substrate and exposing the substrate to extreme conditions capable of corrosion. For this reason, pigments, inhibitors, and other compatible blends are added to the polymer coating formulations to enhance adhesion and protection. To prevent the possible deterioration of inhibitor-spiked polymer coatings, inhibitors are encapsulated through diverse techniques to avoid leakage and to provide a controlled release in response to the corrosion trigger. This review discusses polymer-based coating performance in corrosion-causing environments to protect metals, focusing more on commercial steels, a readily available construction-relevant material used in extensive applications. It further beams a searchlight on advances made on polymer-based coatings that employ metal–organic frameworks (MOFs) as functional additives. MOFs possess a tailorable structure of metal ions and organic linkers and have a large loading capacity, which is crucial for corrosion inhibitor delivery. Results from reviewed works show that polymer-based coatings provide barrier protection against the ingress of corrosive species and offer the chance to add several functions to coatings, further enhancing their anti-corrosion properties. Full article

Magnesium (Mg) and its alloys are promising materials for temporary bone implants due to their mechanical properties and biocompatibility. The most challenging aspect of Mg-based implants involves adapting the degradation rate to the human body, which requires extensive in vitro and in vivo testing. Given that in vivo tests are significantly more labour-intensive than in vitro and ethics prohibit direct experiments on animals or humans, attempts are commonly undertaken to infer conclusions on in vivo degradation behavior from in vitro experiments. However, there is a wide gap between these tests, and in vitro testing is often a poor predictor of in vivo outcomes. In the development of biodegradable Mg-based implants, considerable efforts are being made to reduce the overall time and cost of in vitro and in vivo testing. Finding a suitable alternative to predict the degradation of Mg alloys, however, remains challenging. We present computational modelling as a possible alternative to bridge the gap between in vitro and in vivo testing, thus reducing overall cost, duration and number of experiments. However, traditional modelling approaches for complex biodegradable systems are still rather time-consuming and require a clear definition of the relations between input parameters and the model result. In this study, Kriging surrogate models based on the peridynamic in vitro degradation model were developed to simulate the degradation behavior for two main alloys, Mg-5Gd and Mg-10Gd, for both in vitro and in vivo cases. Using Kriging surrogate models, the simulation parameters were calibrated to the volume loss data from in vitro and in vivo experiments. In vivo degradation of magnesium has one order of magnitude higher apparent diffusion coefficients than in vitro degradation, thus yielding the higher volume loss observed in vivo than in vitro. On the basis of the diffusivity of the Mg${}^{2+}$ ions modeled under in vitro degradation, Kriging surrogate models were able to simulate the in vivo degradation behavior of Mg-xGd with a ratio between 0.46 and 0.5, indicating that the surrogate-modelling approach is able to bridge the gap between in vitro and in vivo degradation rates for Mg-xGd implants. Full article

Hydrogen, due to corrosion processes, can degrade high strength steels (HSS) through embrittlement and stress corrosion cracking mechanisms. Scanning Kelvin probe (SKP) mapping of surface potential was applied, to visualize the locations with an increased subsurface concentration of hydrogen in mild steel and martensitic HSS. This work can help to determine the reasons behind hydrogen localization in a steel microstructure, leading to embrittlement and hydrogen-assisted cracking. Cathodic charging was used to insert hydrogen, which decreased the steel potential. Hydrogen effusion in air passivates steel, increasing the potential of HSS and mild steel. The passivation of steels was monitored depending on different conditions of cathodic pre-charging and the amount of absorbed hydrogen. The SKP could determine the area of diffusible hydrogen and the area of cracks. In addition, low potential locations linked to the hydrogen trapped in the deformed HSS microstructure were also determined, which delayed the steel passivation. Mild steel showed a uniform potential distribution related to interstitial hydrogen, without potential extremes attributed to locally accumulated hydrogen. Thus, SKP sensing can detect locations containing increased concentrations of hydrogen and sensitive to steel cracking. Full article

A critical review is presented on modeling of the radiolysis of the coolant water in nuclear power reactors with emphasis on ITER. The review is presented in two parts: In Part I, we assess previous work in terms of compliance with important chemical principles and conclude that no model proposed to date is completely satisfactory, in this regard. Thus, some reactions that have been proposed in various radiolysis models are not elementary in nature and can be decomposed into two or more elementary reactions, some of which are already included in the models. These reactions must be removed in formulating a viable model. Furthermore, elementary reactions between species of like charge are also commonly included, but they can be discounted upon the basis of Coulombic repulsion under the prevailing conditions (T < 350 °C) and must also be removed. Likewise, it is concluded that the current state of knowledge with respect to radiolytic yields (i.e., G-values) is also unsatisfactory. More work is required to ensure that the yields used in radiolysis models are truly “primary” yields corresponding to a time scale of nanoseconds or less. This is necessary to ensure that the impact of the reactions that occur outside of the spurs (ionizing particle tracks in the medium) are not counted twice. In Part II, the authors review the use of the radiolysis models coupled with electrochemical models to predict the water chemistry, corrosion potential, crack growth rate in Type 304 SS, and accumulated damage in the coolant circuits of boiling water reactors, pressurized water reactors, and the test fusion reactor, ITER. Based on experience with fission reactors, the emphasis should be placed on the control of the electrochemical corrosion potential because it is the parameter that best describes the state of corrosion in coolant circuits. Full article

Cathodic protection efficiency of complex carbon steel structures in confined seawater environment was studied using a specific experimental device. Schematically, this device consisted of a Plexiglas matrix, crossed by a channel 50 cm long, 5 mm deep, 1.5 to 5 cm wide, which moreover included four bends at 90°. Seawater flowed continuously inside the channel over 12 steel coupons embedded in the Plexiglas matrix. Cathodic protection was applied at a constant potential of −1060 mV vs. Ag/AgCl-seawater with respect to a reference electrode located outside the channel, at the seawater flow entry. The potential of four selected coupons was monitored over time via a microelectrode set close to each coupon. It varied significantly with the distance separating the coupons from the channel entry. At the end of the 3.5-month experiment, a polarization curve was acquired. The residual corrosion rate under cathodic protection was estimated via the extrapolation of the anodic Tafel line. It varied from <1 µm yr⁻¹ to 16 µm yr⁻¹, depending on the potential reached by the coupon (between −900 and −1040 mV vs. Ag/AgCl-seawater) at the end of the experiment and on the properties of the calcareous deposit formed on the steel surface. Full article

Organic-inorganic coatings based on polymethyl methacrylate (PMMA)–silica–lithium are an efficient alternative to protect metals against corrosion. Although the preparation methodology is established and the thin coatings (~10 µm) are highly protective, the use of an environmentally friendly solvent has not yet been addressed. In this work, PMMA–silica coatings were synthesized using 2-propanol as a solvent and deposited on aluminum alloy AA7075, widely used in the aeronautical industry. Different concentrations of lithium carbonate (0–4000 ppm) were incorporated into the hybrid matrix to study the structural and inhibitive effects of Li⁺ in terms of barrier efficiency of the coatings in contact with saline solution (3.5% NaCl). Structural and morphological characterization by low-angle X-ray scattering, X-ray photoelectron spectroscopy, atomic force microscopy, thermogravimetric analysis, thickness, and adhesion measurements, showed for intermediate lithium content (500–2000 ppm) the formation of a highly polymerized PMMA phase covalently cross-linked by silica nodes, which provide strong adhesion to the aluminum substrate (15 MPa). Electrochemical impedance spectroscopy (EIS) results revealed an excellent barrier property in the GΩ cm² range and durability of more than two years in a 3.5% NaCl solution. This performance can be attributed to the formation of a highly reticulated phase in the presence of Li, which hinders the permeation of water and ions. Additionally, the self-healing ability of scratched samples was evidenced by EIS assays showing a fast Li-induced formation of insoluble products in damaged areas; thus, constituting an excellent eco-friendly solution for corrosion protection of aerospace components. Full article

Environmental cracking- and fatigue-related failures threaten all major industries and, to combat such degradation, numerous residual stress impingement (RSI) methods have been developed with varying levels of efficacy and ease of use. Some of the most commonly used RSI methods, such as shot peening, laser shock peening, and low plasticity burnishing, as well as new methods, such as ultrasonic nanocrystal surface modification, are reviewed in the context of corrosion, corrosion fatigue, and environmental cracking mitigation. The successes and limitations of these treatments are discussed, with a focus on their efficacy against these three damage modes based on the available literature. Case studies are reviewed that demonstrate how these treatments have been adopted and advanced by industry, and application-specific research efforts are explored with a focus on future opportunities. Research is identified that illustrates how the utility of these surface treatments may vary between alloy systems, and where the benefits must be weighed against the risks to a component’s service performance. Full article

Corrosion-induced maintenance is a significant cost driver and availability degrader for aircraft structures. Although well-established analyses enable assessing the corrosion impact on structural integrity, this is not the case for fatigue nucleation and crack growth. This forces fleet managers to directly address detected corrosion to maintain flight safety. Corrosion damage occurs despite protection systems, which inevitably degrade. In particular, pitting corrosion is a common potential source of fatigue. Corrosion pits are discontinuities whose metrics can be used to predict the impact on the fatigue lives of structural components. However, a damage tolerance (DT) approach would be more useful and flexible. A potential hindrance to DT has been the assumption that corrosion-induced fatigue nucleation transitions to corrosion fatigue, about which little is known for service environments. Fortunately, several sources indicate that corrosion fatigue is rare for aircraft, and corrosion is largely confined to ground situations because aircraft generally fly at altitudes with low temperature and humidity Thus, it is reasonable to propose the decoupling of corrosion from the in-flight dynamic (fatigue) loading. This paper presents information to support this proposition, and provides an example of how a DT approach can allow deferring corrosion maintenance to a more opportune time. Full article

The corrosion performance of Aluminium (Al) and zinc (Zn) is of interest in repositories for radioactive waste as the production of hydrogen gas during their anoxic corrosion may create open pathways for the transport of radioactive ions. Al and Zn rods were embedded in concrete cylinders and immersed in artificial groundwater at anaerobic conditions for 2 weeks and up to 2 years in laboratory conditions. Corrosion rates were determined to enable predictions and estimations of risks for gas evolution and the assessment of the potential impact of corrosion on the structural integrity of concrete in the final repository of low and intermediate level metal-containing waste from dismantled nuclear power plants. Samples were collected after 2, 4, 12, 26, 52 and 104 weeks. The observed corrosion rates were higher for Al compared with Zn, as expected, but both materials revealed comparatively high initial corrosion rates that decreased with time, reaching steady state after 26–52 weeks. Some of the Al containing concrete cylinders were cracked as a result of the corrosion processes after 2 years of exposure, thereby providing free passage between the embedded metal and the surrounding environment. No such effects were observed for Zn. Comparative studies were performed on non-concrete-embedded Al and Zn immersed in artificial groundwater. Observed long-term corrosion rates (1–2 years) were similar to corresponding corrosion rates in concrete. The results indicate that immersion studies in artificial groundwater can be used to estimate the long-term corrosion performance of Zn and Al in concrete. Full article

Corrosion of the reinforced concrete (RC) structures has been affecting the major infrastructures in U.S. and in other continents, causing the recent several bridge collapses and incidents. While the theoretical understanding is well-established, the reliable prediction of the corrosion process in the RC structural systems has hardly been successful due to the inherent uncertainties existed in the electrochemical corrosion process and the associated material and environmental conditions. The paper proposes a computational framework to develop evidence-based probabilistic corrosion initiation models for the reinforcing steels in the RC structures, which predicts the corrosion initiation time and quantifies the inherent variances considering various acting parameters. The framework includes: probabilistic modeling with Bayesian updating based on the sets of previously generated experimental data; Bayesian model/parameter selection considering various parameters, such as material properties and environmental conditions; corrosion reliability analyses to predict the probabilities of the corrosion initiation at given time t, structural configurations, and environmental conditions; and sensitivity analyses to measure and to rank the influences of each acting parameter and its uncertainty to the probabilities of the corrosion initiation. Total of 284 sets of experimental data exposed to the coastal atmospheric environments are used for the modeling. The goal of the Bayesian model selection presented in this paper is to obtain the most accurate and unbiased model using the simplest form of expression. The developed example corrosion model is currently limited to the initiation of diffusion-induced corrosion. The model can be updated, improved, or modified upon future available sets of data. The research contributes to the decision making to improve the corrosion reliability, corrosion control, and further the structural reliability of corroding structures. Full article

This article presents a synthesis of recent studies focused on the corrosion product layers forming on carbon steel in natural seawater and the link between the composition of these layers and the corrosion mechanisms. Additional new experimental results are also presented to enlighten some important points. First, the composition and stratification of the layers produced by uniform corrosion are described. A focus is made on the mechanism of formation of the sulfate green rust because this compound is the first solid phase to precipitate from the dissolved species produced by the corrosion of the steel surface. Secondly, localized corrosion processes are discussed. In any case, they involve galvanic couplings between anodic and cathodic zones of the metal surface and are often associated with heterogeneous corrosion product layers. The variations of the composition of these layers with the anodic/cathodic character of the underlying metal surface, and in particular the changes in magnetite content, are thoroughly described and analyzed to enlighten the self-sustaining ability of the process. Finally, corrosion product layers formed on permanently immersed steel surfaces were exposed to air. Their drying and oxidation induced the formation of akaganeite, a common product of marine atmospheric corrosion that was, however, not detected on the steel surface after the permanent immersion period. Full article