Values of electrochemical parameters for Stainless Steels in artificial seawater, at 26ºC and pH 8.2 
A major concern in the design of engineering structures is the ability of components to maintain their integrity during their entire life service even when subjected to a combination of fluctuating loads and aggressive environments. The requirement for reliable structural integrity is particularly important for structures, involved in fundamental fields such as transportation, oil and gas production and energy generation. Fatigue and corrosion fatigue failures take place in components and structures as result of complex loading histories. There are different stages of fatigue damage in engineering components where defects may nucleate on initially smooth or undamaged sections, followed by microstructural crack formation, stable propagation and finally unstable crack propagation where catastrophic failure occurs.
Total fatigue life is often considered as a process of fourth major stages [1,2]:
Initiation or nucleation of fatigue cracks: substructural and microstructural which cause nucleation or permanent damage,
Small-Crack growth: the creation and growth of microscopic cracks,
Macro-Crack propagation: the growth and coalescence of microscopic flawsto form “dominant cracks” and stable propagation of dominant macrocracks
Final fracture: structural instability or complete fracture.
Then, fatigue life of engineering components and structures can be deﬁned as the period during which cracks initiate from defects and propagate. The largest fraction of fatigue life is spent in the crack propagation stage. However, when engineering structures operate under severe conditions, the problem of fatigue failure is raised, especially in presence of aggressive environments. Under such severe conditions, the crack initiation stage is dramatically reduced as the case of structures in marine environments.
On the other hand, the stresses operating on structures can be mechanically applied (constant or cyclic), residual, and in some cases, thermal which depend on the operation conditions.
Stainless steels are an important group of materials for diverse engineering applications. This kind of corrosion resistant materials was introduced with the aim of reducing maintenance costs involved with materials such ascarbon steel. However, there are several cases around the world, [3-8] in which the failure frequency of stainless steel piping systems on offshore platforms is very high, resulting in unacceptable maintenance costs.
Unfortunately the degradation process is more complex than just localized electrochemical reactions at the metal surface. It is documented [5,9,10] that the corrosion of stainless steels (SS) is more severe in natural seawater than in sterile or synthetic seawater due to microorganisms activity. There is agreement among researchers that the increased corrosion is due to biofilm formation [4,5,7,8] Electrochemical reactions are influenced by the chemical micro-environments generated by formation of biofilms at the metal surface. In seawater applications, the most widely used stainless steel grade, namely, 316L, suffers from localized corrosion. Even the substantial amount of data published about studies of localized corrosion of 316 and 316L stainless steels, frequently affected by pitting and crevice corrosion, the problem of structural failure in marine environments remains.
An outstanding problem in corrosion science and engineering involves the prediction, of damage caused by corrosion fatigue during the early stages of damage. This problem is particularly important because localized attack, such as pitting corrosion fatigue (PCF), normally occurs on passive alloys with minimal metal weight loss, and is commonly detected when the failure of the component is complete.
The most important aspect of corrosion fatigue assessment on components and structures in real service is the prediction of their residual life when there is a risk of undergoing localized attack as precursor of fatigue cracks. The conventional fracture mechanics tools are limited to provide information concerning the type and rate of damage occurring during the early stages of damage and consequently provide limited insight into the mechanism of pitting corrosion fatigue failure process. It is important to understand the role of the environment on the early stages of corrosion fatigue damage. In this sense, very sensitive electrochemical techniques have been used in corrosion fatigue studies by the authors of this chapter, where the main aim has been to determine the early stages of corrosion fatigue damage. This chapter presents a review of information obtained from applied sensitive electrochemical techniques to stainless steels exposed to seawater and chloride ions media to observe Early Corrosion Fatigue Damage.
2. Corrosion fatigue
It must be recognized, however, that there is no generally accepted definition as to what constitutes initiation or when the initiation phase is complete and propagation commences. The net cycles to failure represents the sum of both, crack initiation and propagation.
The complex task associated with fatigue resistance evaluation is the fact that individual factors may be synergically interactive, so a change in one must be assumed to affect the role of the others. Thus, the accumulation of damage during the fatigue lifetime of a component depends not only on its load history, but also of the synergistic effects of stress and surrounding environment [13,14]. Then, corrosion fatigue is defined as a synergistic effect in which corrosion and fatigue occur simultaneously. The combined effect of an aggressive environment, such as seawater, with a cyclic stress or strain is, invariably, more severe than the sum of the two effects of corrosion and fatigue acting separately. The effect of the environment on fatigue resistance is well documented in the form of stress vsnumber of cycles to failure (
Fatigue and CF studies address the following regimes:
LEFM (long crack) regime, were cracks are of the order of millimeters (i.e. propagation)
EPFM (physical short cracks) regime, were cracks of the order hundreds of micrometers
MFM (short crack) regime, were cracks of the order of tends of micrometers develop early in the lifetime and exhibit growth rate variations through the microstructure (i.e. nucleation).
The most important aspect of corrosion fatigue assessment on components and structures in real service is the prediction of their residual life when there is a risk of undergoing localized attack as precursor of fatigue cracks.
In passive alloys, it is recognized that pitting corrosion plays a very important role in CF crack initiation [16, 17, 19]. CF lifetime prediction turns complex because of the need to account main processes leading to fatigue failure from a 'defect-free' surface [14, 20], where the early corrosion fatigue damage includes:
breakdown of the surface passive film
pit initiation and growth,
transition from pit to short crack nucleation,
short crack growth
The selection of the techniques used to evaluate and study corrosion depends on the kind of corrosion taking place. The principal aim of the corrosion scientist is to determine the mechanism of the corrosion process including intermediate reactions and the kinetics of these processes. Sometimes it is necessary to use intrusive methods (electrochemical methods) in which the system is stimulated externally and the response of the system to that perturbation is measured. Other techniques are able to measure electrochemical activity without the necessity of any kind of externalperturbation to the system, the electrochemical noise technique (ENT), the scanning reference electrode technique (SRET) and scanning vibrating electrode technique (SVET) are examples of non-intrusive techniques. The most important aspect of corrosion assessment on components and structures in real service is the prediction of their residual life when there is a risk of undergoing localized attack. In that respect the use of electrochemical methods for studying localized corrosion is an important part of the evaluation since the kinetics of localized corrosion is different with respect to general (uniform) corrosion.
From a structural integrity point of view general corrosion does not represent a serious problem for the corrosion engineer due to the fact that stress concentrators are not generated. Therefore general corrosion can be assessed using basic electrochemistry concepts and techniques [21,22]. In the case of localized corrosion, the measurement of the corrosion rate becomes more complicated due to unequal anodic and cathodic area ratios and therefore the effects of this kind of damage on the structural integrity of structures are much more severe.
2.1. Localized corrosion concepts
Due to their recurrent nature, localized corrosion processes often cause major practical problems affecting the performance of technologically important metallic materials, like stainless steels, nickel, aluminium, and many others metals and their alloys in different environments, especially those containing chlorides.
It can be considered that the corrosion process results from changes in the nature and composition of metals exposed to environments of homogeneous composition. The point of interest is “what happens when metals with approximately uniform composition are exposed to electrolytic environments in which composition changes makes them heterogeneous, e.g. differential aeration?" In this case we are dealing with concentration cells, i.e. localised corrosion.
One of the established essential principles of corrosion is that: The sum of the rates of the cathodic reactions must be equal to the sum of the rates of the anodic reactions, irrespective of whether the attack is uniform or localized , so the following equation must be satisfied:
whereIc and Ia denote the cathodic and anodic currents respectively which has a direct relation with the reaction rate of the electrochemical process.
If it is considered that the attack is uniform and assuming that there is only a single predominant anodic and cathodic reaction, then:
whereia and ic are the anodic and cathodic current densities assuming the area of the cathode Sc equals the area of the anode Sa.
When the corrosion attack is localized the anode area is very small compared with the cathode area, Sa<Sc and as a consequence ia>ic, and the larger the ratio ia:ic, the more intensive the attack. Thus localized attack usually involves a corrosion cell consisting of a large cathodic area and a small anodic area.
It is now known that many aqueous corrosion processes of great technical interest occur under conditions in which the access of electrolyte is restricted. This can be due to the special geometry of the corroding material e.g. structures with riveted plates, flange joints, gaskets; and also due to the existence of some deposits such as corrosion products or scales on the corroding surface. In the cases where corrosion occurs under conditions of restricted diffusion, the chemical composition of the corroding environment inside the occluded cavity may be very different from that of the composition of the bulk solution. One of the most important effects is that changes in oxygen or ionic concentration in the electrolyte give rise to changes in corrosion potential. Under normal circumstances where the aggressive environment is aerated, the surface of the corroding alloy outside the occluded cavities is often passive as a result of the formation of an oxide film of corrosion products. Passivation takes place at these sites because they are in direct contact with the oxygen dissolved within the electrolyte. These surfaces act as aerated cathodes where oxygen takes part in the reduction reaction of the corrosion process. In this reaction the oxygen is reduced with the consequent increase of pH according to the following reaction for the case of basic or neutral solutions :
or in a solution of low pH:
The surface, which is inside the occluded cavity, is active and acts as anode as a consequence of the very low concentration of oxygen in the solution inside the cavity. At these surfaces the metal undergoes dissolution. Additionally, the hydrolysis reaction takes place with a decrease in the pH of the solution according to the following reaction sequence:
Much effort has been made in the last 40 years for a better understanding of the processes involved in localized corrosion, the majority of these studies being focusedprincipally on aspects of the growth and stability of the sites undergoing localized attack. On the other hand, the mechanisms of nucleation and early stages of damage are not yet completely understood.
An important improvement on the present state of knowledge is achieved when the global process of localized corrosion can be partitioned into a nucleation stage (initiation), and a successive metastable growth stage, which eventually is followed either by rapid repassivation or stable pit growth. If the active condition inside a crevice or pit is stable over a longer period of time, rapid metal dissolution usually takes place. The rate controlling reaction during the localized corrosion processes such as activation, diffusion, or ohmic control, has a significant influence on the shape and geometry of the crevices or pits produced.
The theoretical models, that have been proposed to describe the initiation of the localized corrosion process, can be grouped into [24,25]:
Ion migration and penetration models
Mechanical film breakdown theories.
Substantial research has been carried out to study the structural parameters involved in localized corrosion processes. From these, it has been demonstrated that defects in the metal structure, such as non-metallic inclusions or dislocations may generally act as sites for pit initiation on passive metal surfaces . Stainless Steels (SS’s) with higher concentrations of alloying elements were found to have an increased pitting resistance due to the formation of passive films containing fewer defects and greater stability.
Despite the efforts made to understand this phenomenon, localized corrosion is a non-predictable degradation process of metals and alloys in contact with aggressive environments. Given that most of the information related to the stable stage of localized corrosionhas been obtained throughout studies of pitting and crevice corrosion, this aspect of the localized attack will be presented in the next section dedicated to pitting corrosion.
3. Pitting corrosion fatigue
3.1. Breakdown of the surface passive film
Corrosion is an electrochemical reaction process between a metal or metal alloy and its environment , which involves complex mass and charge transfer taking place at the metal-electrolyte interface. These charge transfer reactions at the interface are the origin of the instability of metals. The high corrosion resistance of Austenitic SS’s is primarily attributed to the adherent metal-oxide film formed on its surface called passive film. This natural coating acts as a barrier that avoids the contact between fresh metal surface and the electrolyte limiting the corrosion reactionand such alloy is said to be passive. When stainless steels are exposed to oxygen containing electrolytes, a chemically stable, non soluble film is formed from a mixture of iron and chromium oxides, with hydroxide and water-containing compounds located in the outermost region of the ﬁlm, and chromium oxide enrichment at the metal-ﬁlm interface . However, the resistance of this passive ﬁlm is determined by the environmental conditions to which the SS is exposed to, as well as by the alloy composition. Many metals and alloys become covered with oxide films on exposure to aqueous environments. Copper, aluminum or tin and their alloys develop thick films, while metals which exhibit passive behaviour like stainless steels have a very thin film of the order of 9 to 20 nm. The passive films are cathodic to the metal matrix. However, the susceptibility of passive films to suffer local breakdown depends upon the nature of the film, the quantity and nature of non metallic inclusions, the chemical composition of the electrolyte or solution, and the electrochemical state at the metal/solution interface, but also to a possible stress state.
For CF test, when the passive metal or alloy is subjected to cyclic loading, the passive film is damaged mechanically due to the creation of slip steps from beneath and following a repeated process of microdeformation-activation-dissolution-repassivation.
During the initial cyclic loading, fine slip lines appear on the specimen surface because dislocations, at or near the surface, the stress in localized sites can exceed the nominal stress. By using microscopic techniques has been possible to observe localized plasticity at microscopic scale in the grains, where fatigue damage is caused by microplasticity produced by large shear stresses.
Processes of nucleation and formation of fatigue slips bands often precedes at grain boundaries as is shown in figure 2. Mughrabi et al.  showed that nucleation at grain boundaries occur at sites where persistent slip bands (PSBs) impinge.
In smooth surfaces of SS’s, during the early corrosion fatigue damage, the permanent slip bands are associated with breakdown of the passive film. The breakdown of the passive film causes dissolution of the non-covered active metal in contact with the electrolyte, which acts as a small anode against the large cathodic. This small anode is a vulnerable area on the metal surface, where a high local metal dissolution takes place, and leading cavities such as pits and/or crevice. Extensive development of techniques to study electrochemical reactions have simulated the analysis of potential and current fluctuations taking place during electrochemical processes which are translated in to electrochemical noise (EN) signals.
EN is defined as spontaneous fluctuations in current and potential generated by corrosion reactions [30-34]. In this context, the study of spontaneous current or potential fluctuations to characterize corrosion processes have received considerable attention, such as the study of corrosion potential (Ecorr) and current fluctuations applied to monitor the onset of events characterizing pitting [35-36] or stress corrosion cracking (SCC) [37-39] The noise is typically measured potentiostatically, galvanostatically, or in a Zero Resistance Ammeter (ZRA) mode [30,31,34]. With ZRA mode, both the potential and current fluctuations can be measured using two nominally identical electrodes, connected through a ZRA; where a net current and changes in the potential are observed at free corrosion conditions according to the corrosion process.
During the Corrosion Fatigue tests conducted in natural seawater , the potential time series obtained from electrochemical noise measurements had a common characteristic pattern of quick drop and slow recovery. Common explanations for these patterns of quick drop and slow recovery have been associated to anodic dissolution, passive film breakdown, metastable and stable pitting corrosion, or with the crack initiation and crack growth due to microstrain and local mechanical stress conditions .
The figure 3 shows patterns of quick drop and slow recovery, indicating that passive film eventually is broken, due to applied mechanical stress and the interaction with the electrolyte, turning it in an active dissolution of metal. Also, on figure 3, the surface damage after
3.2. Pit nucleation and growth
According to Szklarska-Smialowska , the susceptibility of a metal or alloy to pitting can be estimated by determination of one of the following criteria:
Characteristic pitting potential
Critical pitting temperature,
Number of pits per unit area, or weight loss and
The lowest concentration of chloride ions that may cause pitting
One of the most important parameter to determine an alloy’s susceptibility to pitting corrosion is the pitting potential, i. e., the potential at which the passive film starts to break down locally. The potential above which pits nucleate is denoted by Ep and the potential below which pitting does not occur and above which the nucleated pits can grow is often indicated by Epp (Figure 4 and Table 1).
As mentioned above, pitting corrosion involves localised attack of very small areas of metal surface undergo localisedattack whilst the rest of the surface is largely unaffected and remains passive. Pitting is a particularly insidious form of localized corrosion because
the extent of metal dissolution reaction is small but the attack is rapid and penetrates into the metal. The location of pits on metals that develop passive films is often unpredictable, and the pits tend to be randomly dispersed on the metal surface [41-43]. However, Sedriks[44,45] indicates the importance of different types of heterogeneities at the material surface during pit initiation, because the location of pits is to some extent defined by the microstructure of the alloy and the geometry of the system. In chloride containing aqueous solutions, the uniform corrosion rate of stainless steels in the passive state is insignificant, i.e. 0.15 to 15.0 μm per year . However, pitting corrosion of this type of alloys is very common in these environments , where the local dissolution rate of metal can be up to 12 mm per year .
Pitting corrosion can occur when a local breakdown of the passive film takes place in an aqueous solution on a microscopic scale (nucleation process). This process involves small and sudden increments of anodic current, which are characterized by current spikes, leading to oxidation and dissolution of less than 0.01 μm3 of metal. The nucleation process is unstable and in most cases it will stop by the regenerationof the passive film. Another possibility is that a nucleation event develops into the second stage of initiation, i.e. the metastable pit growth. During this step, a gradualand bigger increase of the anodic current takes place. This stage stops if repassivation of the micro-pit occurs. A volume of up to several μm3 of metal can be dissolved in stainless steel during the metastable growth. In some cases the metastable pit growth precedes stable pitting. On the other hand, if repassivation of metastable micro-pit does not occur, the growth of stable pits can take place (figure 5).
Measurements of the physical separation of anodic and cathodic areas, the currents flowing between them as well as the mapping of potentials in electrolytic solutions have been successfully used for the study of the processes of localized corrosion of different systems [47-53]. A schematic drawing of a local corrosion cell is shown in figure 6.
With the aim of determining the velocity of metal dissolution directly in active pits during pitting corrosion, Rosenfeld and Danilov, designed an apparatus to measure the field strength in the electrolyte directly above an active pit. They employed a twin probe method by using two reference electrodes, which makes it possible to measure the potential difference ∆E in any direction between two points in the electrolyte with the aid of two non-polarizable electrodes, for example calomel electrodes.
The equipment used for the measurements of the potential difference ∆E (ohmic potential gradients) is called the Scanning Reference Electrode (SRET). With the measurement of the electric field strength in the electrolyte over the pits it was possible to determine the current flowing from the anode points, based on the fact that, the vector of the normal component of the current density at a pre-determined point (i') in a uniform field is equal to the product of the electric field strength E and the specific conductivity of the medium κ. The resolution of the SRET depends upon the proximity of the scanning probes to the corroding sites and the magnitude of the corrosion currents from each site. As shall be shown later, the distance between the probe and specimen surface and the conductivity of the solution governs the sensitivity of the technique. It has been reported the capability of the SRET to identify the position of localized activity in the metal surface however did not report any assessment of pit size or shape from the performed SRET measurements [48-51]. The growth of corrosion pits is the next stage of the localized attack process.
Pit growth law
Pit growth studies have received less attention than its initiation. The kinetics of pit growth is generally assessed by electrochemical and metallographic methods. However, a combination of the two methods is usually preferred. A wide variety of pit growth laws have been reported for different systems metal - electrolyte, but the theory of pits growth remains unclear. Although stainless steel 304 is a very common and extensively used alloy, the determination of pit growth in NaCl solutions at open circuit potential has not been possible in terms of reproducible and reliable measurements. This is essentially due to the tendency for spontaneous repassivation of the pits when the steel is at open circuit potential . An approach has been the determination of the pit growth kinetics on potentiostatically generated pits in specific metal – electrolyte systems. Dzib-Pérez  generated corrosion pits potentiostatically on specimens type 304 SS in stationary conditions in two electrolytes: 3.5% wtNaCl solution (κ=55.8 mS/cm) and natural seawater (κ=50.6 mS/cm). Specimens were initially polarized potentiostatically in natural seawater for 105 s at a potential of 365 mV vs SCE (to induce the formation of pits) and immediately after, the electrode potential was stepped down to a value of 300 mV vs SCE (to induce the growth of the initiallyformed pits avoiding the formation of new pits). The chronoamperometries obtained for 304 steel in natural seawater are shown at Figure 7.
All chronoamperometries obtained showed a rapid increase in current during the time the stainless steel specimen was polarized potentiostatically above the pit potential, which is associated to induced nucleation and fast pitgrowth.
Most of the generated pits quickly repassivated when the potential was stepped down to a potential level below the pitting potential. Under this condition 1 to 3 pits grew steadily until the end of polarisation. The increase of current as a function of time can be associated with two processes taking place under potentiostatic polarization: mainly the active dissolution of nucleated pits (one to three pits) and the simultaneous dissolution of the metal surface in the passive state. From the integration of the area beneath the curve current vs time the electric charge was obtained, from which the quantity of dissolved metal per pit was calculated using Faraday's law according to the chemical composition of the 304 stainless steel .
And the other hand, Figure 8 shows the amount of material dissolved as function of time of anodic polarization, also includes the fit (solid and dotted lines) performed through the following power equation:
Once determined the amount of dissolved material per pit as a function of anodic polarization time and knowing the density of stainless steel (ρ= 8.03 g/cm3), the volume of dissolved metal was determined.Using a material removal procedure described in detail by Gonzalez Sanchez and Dzib-Pérez [40-55] to determine the pit depth as a function of time of anodic polarization the empirical pit growth law was established for corrosion pits in 304 stainless steel. Figure 9 shows the Maximum Pit Depth (
From fitting of these relationships, represented by solid and dotted line, was obtained the empirical equation for the pits growth law for each experimental condition, which has the shape of an exponential equation :
Has been reported that the growth rate of a pit is characterized by a gradual increase in the current at constant potential, which is proportional to t2 or t3. Gonzalez-Sanchez  generated pitting on stainless steel 304 and 316L using the same electrochemical process used in this study. This author reported an empirical equation for the pit-growth law of the form Pd=
316L in artificial seawater,
and for 304 stainless steel, also in artificial seawater, the following equation:
The MPD generated on the 304 stainless steel in artificial sea water, reported by Gonzalez-Sanchez  were slightly lower, but with a trend similar to those obtained by Dzib-Pérez . These forms contribute to assess the first stage of damage (pitting).
Newman  reported the pit growth under potentiostatic polarization on a 304 stainless steel in a 1M NaCl solution containing 0.04 M Na2S2O3. The pits generated had a hemispherical morphology. These authors found good agreement between results obtained via Faraday's law and those obtained from microscopic analysis. Researchers had reported the pits growth under potentiostatic polarization on 304 and 316L stainless steels in artificial seawater (Gonzalez-Sanchez, 2002) and natural seawater . The shape of pits generated at both stainless steels was semi-elliptical [40, 56]. Gonzalez-Sanchez  reported a good agreement between the results obtained from Scanning Reference Electrode Technique (SRET) measurements with those obtained of a method of material removal.
In the present document, pits were generated under potentiostatic polarization on 304 stainless steels in 3.5% wtNaCl solution and in natural seawater as well as at open circuit potential in a solution of 1M FeCl3. The pits generated had hemispherical morphology as seen in Figure 10.
In order to determine the correct morphology (semi-elliptical or hemispherical) of pits generated in this investigation the volume of each pit was calculated according to the geometry of an ellipse or an sphere and compared with results obtained from the chronoamperometries. The results indicate that the volumes calculated based on a spherical geometry are closer to the volume calculated from the chronoamperometry curves, as seen in Figure 11. Therefore, the volume of a pit, obtained from removal of material, calculated according to a spherical geometry was used for comparison and analysis with the results obtained using electrochemical techniques. The values of the volume per pit as a function of growth time were used to calculate the corresponding amount of dissolved material for a pit grown under potentiostatic control on 304 SS in 3.5 wt% NaCl solution and in seawater natural. In Figure 12 shows the amount of dissolved material, determined chronoamperometries and by a method of material removal, as a function of pits growth time on the 304 stainless steel in NaCl solution and in water natural sea. Also, the figure 13 illustrates the pit nucleation and growth process obtained from SRET Maps.
Acuña has observed that on the maximum tensile stress zone of bent-beam specimens, after
3.2. Pit to small crack transition
Pit to short crack transition involves the determination of the critical pit size for the transition from pit to fatigue crack. In this stage, the microstructure and the state of stresses around the corrosion pit play a very important role. The conditions for the pit to crack transition are generally defined phenomenologically by using a Linear Elastic Fracture Mechanics (LEFM) approach. A major concern is that the threshold stress intensity factor range defined for corrosion fatigue cracking is determined considering long cracks and can not be applied to microscopically small cracks (MSC) initiated from pits.
Two criteria are used to describe the transition processes:
the stress intensity factor associated with the equivalent surface crack growth at which the corrosion pit reaches the threshold stress intensity factor for the fatigue crack growth,
Corrosion fatigue crack growth rate also exceeds the pit growth rate,
Akidet. al.  have shown that in some cases pit development overcomes the nucleation stage of the corrosion fatigue cracking process. However, it appears that transition from pit to short fatigue crack occurs at some critical size associated with microstructure, applied stress level, mode of load and stress state around the pit. In order to describe the stress state and the stress intensity conditions around the pit, several models, based in pitting corrosion fatigue mechanisms have been proposed [58-61]. They have been assumed that corrosion pits behave as sites for fatigue crack initiation through a purely mechanical micro-notch effect in smooth surfaces. Real components are normally undergoing complex stress conditions which induce mixed loading modes; where it has been reported that the threshold stress intensity factor for short fatigue cracks in structures subjected to mixed loading modes is lower than for structures subject to simple loading mode conditions .
The general aim of this section is dedicated to determine the influence of mixed stress conditions on the initiation of fatigue cracks from corrosion pits. Here we present the results obtained from the analysis of the stress state and the threshold stress intensity around hemispherical corrosion pits developed on austenitic stainless steel samples immersed in natural seawater. The concept of pits as surface semi-elliptic cracks is introduced throughout a linear elastic fracture mechanics analysis. Pit depth to major mouth axes ratio (a/c) and the effect of stress orientation were analyzed in terms of variations of the stress state and mixed load modes. Also the pit to short crack transition and short crack growth is reported through sensitive electrochemical techniques.
From the SEM analysis conducted on the metallic specimens after 15 days of immersion in natural seawater, semi-elliptic corrosion pits with different depth /major mouth axes (a/c aspect ratio) values: 0.33, 0.47, 0.56, 0.62 and 0.74 were found. Figure 15 presents corrosion pits formed on the surface of a specimen after
Pits developed on grain boundaries, mainly at triple point grain boundary. Small cracks (~ 5 μm long) had grown from nucleation sites (Figure 15c). From the earliest stage, the cracks grew by interconnecting several smaller cracks following the grain boundary pattern. Crack nucleation events and the early crack growth could be associated with the patterns of quick drop and slow recovery, of amplitudes of 20 and 70 mV and current density between 0.10 and 0.60 μA/cm2 where these signals had higher intensity and higher frequency. Small cracks could grow from a multitude of nucleation sites and coalesce to form large cracks in a relatively short time. Large intergranular crack growth events can be associated with those patterns of 200 mV in amplitude and a cathodic current density of 8.0 μA/cm2 (in the figure 15 (a) indicated with ellipses on the potential and current EN patrons). The potential transients could be the result of crack wall dissolution and a possible long active dissolution out of the crack, associated to current transients related to cracking by the reduction processes, where the cathodic reaction consumes electrons that are removed from the surface and the electrochemical double layer present on metal surface, both external to the crack and on the crack walls.
In order understand the role of cyclic stress on pit development and growth, local electrochemical measurements were made using SRET on tubular samples of 316L steelimmersed in 0.05%FeCl3 solutionpH~1.9, conductivity 11.6 mS/cm; under fatigue conditions with an applied stress range of 185 MPa (75%
The current density at which the pit–crack transition occurs can then be used to determine the threshold stress intensity for the onset of cracking for damage from smooth surfaces. Figures 15(a) and 16(a) indicate that the first period was dominated by pitting corrosion and the CF cracks incubation took place; the second period corresponds to the nucleation and initial growth of short CF cracks from grain bonding triple points which is associated with a drastic decrease in potential (15 (a)) and current (16(a)). And finally, the third period where the electrochemical current noise signal recovered a synchronized pattern and also the current density from SRET measurements presented a change to higher values that may be related to the arrest of the CF cracks as their Faradaic contribution disappeared.
As above mentioned, the pit to a small crack transition is not governed solely by the stress distribution around the defect (pit), but is also determined by the local electrochemistry which controls pit growth, all together in a synergic phenomenon. We suggest that despite the solution chemistry is not be the same in large cracks as that found in inside a pit, and the microplasticity is generated by the stress concentration generated by the pit geometry for the case of austenitic stainless steels (susceptible to work hardening), the ΔKth is a parameter that could be used to determine the stress intensity around of pit and pit contour. There are basically two reasons why the cyclic plastic deformation is higher just at the surface: concentration of plastic deformation due to higher stresses near the surface, and the low constraint on near-surface volumes of cyclically loaded material. In complex engineering components, higher surface stresses result from either micronotches (i.e. pits) or bending and twisting, both of which lead to stress gradients with the highest stress on the surface. Usually, under conditions of uniaxial load, the geometry of a pit-like crack tends to keep a semicircular shape, whereas for the case of bending load, the surface cracks adopt a semi-elliptic configuration during their propagation . It is for this reason that the direction of the applied stress plays an important role in the nucleation and propagation of fatigue cracks from corrosion pits.
In this section, the threshold stress intensity factor range (Δ
Redefining the coordinate system to make the new axes coincide with the pit-like crack orientation, it is possible to resolve the applied stress on normal and tangential components. The relationship between the transformed stresses and the normal applied stress are given for equations (13) and (14).
The stress components associated to the plane x’y’ where the crack is located are
where a/c is ≤ 1, and
The value of the threshold stress intensity factor for load mode II (
Equations 15, 16 and 17 were used to determine the stress intensity factor for load mode I, II and III respectively developed at the pit contour defined by the angle φ: (φ = 0˚, φ = 45˚ and φ = 90˚). Considering two different normal applied stress values
Table 3, presents the values of ΔKI, ΔKII and ΔKIII as a function of the orientation angle
In order to define the conditions for the initiation of fatigue cracks from pits on components subject to mixed load modes, a direct equivalence of stress intensity factor to the energy approach was considered. The approach where the elastic strain energy release rate (
Equation 18 indicates that
Figure 20 shows the values of the ΔG as a function of the orientation angle for different locations along the pit contour: at the surface
The fracture resistance value
The orientation of the applied stress plays an important role in the nucleation and propagation of fatigue cracks from this kind of surface flaws (Figure 21). The asymmetry of the applied load induces normal and tangential stresses which along with the aspect ratio have a strong influence on the stress intensity factors which is observed in the variation of
For angles lower than 30, tension stress are favoured (load mode I) and become the dominant stress.The orientation of the stress in an angle relative to the pit-like crack plane generates a normal tension stress at the microscopic plane of the crack that can be even higher than the externally applied stress. This induces a stress singularity that makes theperpendicular tension stress component sufficiently high toactivate the crack initiation from the pit.
The analysis indicates that
Stress and strain distributions are viewed perpendicular to loading axis. Equivalent Von-Mises Stress and (b) total deformation of a pit with pit depth Pd=168μm. The plane stress had been assumed in the present analysis and the stress distribution around of semi-elliptic pit-like crack was done by considering biaxial loading conditions. Figures 22 and 23 show the Finite Element Analysis performed using ANSYS 11.0 . A 3-D version of a thin-walled 350 μm tube specimen was modeled and pits were created half way along the length of the specimen. A reﬁned mesh was developed in the region around the pit to enhance the accuracy of stress and strain predictions. The von Misescriterionmodel was used in the analysis to characterize the elastic-plastic behaviour of the material. The FE model was applied to a hemispherical shaped pit of 168 μm, 274 μm and 291 μm deep. The aspect ratio is found to generally increase with increasing pit depth. Table 4 reports the results of ΔK and ΔG obtained for 3 pits depth configuration.Pit shape was obtained by a method of material removal and after modelled using Finite Element Method.
Specimen under cyclic loading at a stress level around 90%
This plastic strain at pit bottom induces higher constrain than those observed just near to wall pit surface. Therefore, the pit to short crack transitions is done closer to the pit wall surface, as is shown in figure 22.
From figure 21 and table 3, it can be seen that for load mode I, when
Tangential stress has a coupled influence with tension stress for angles from 30º to 55º (load modes I and II). For angles lower than 30, tension stress are favoured (load mode I) and become the dominant stress.
The orientation of the stress in an angle relative to the pit-like crack plane generates a normal tension stress at the microscopic plane of the crack that can be even higher than the externally applied stress. This induces a stress singularity that makes the perpendicular tension stress component sufficiently high to activate the crack initiation from the pit. Based on the observations about the stress conditions around the pit-like cracks, the direction for crack initiation will be a function of the ratio, due to that the normal and tangential stresses vary with the orientation angle. Thus a crack will preferentially nucleate at sites of maximum principal normal stress as is indicated in figure 22 (a) and corroborated by figure 22 (b).
From results obtained on corrosion fatigue tests using Electrochemical Noise and SRET, it was possible to determine the pit initiation time, pit activity and pit localization on specimen surface. The changes in dissolution current obtained from SRET measurements and the increment in the amplitude and frequency of potential transients observed through the Electrochemical Noise tests, gave semi-quantitative information of the early stages of corrosion fatigue damage and cracking. Despite the inability to spatially resolve either the pit or crack size or shape from SRET measurements in FeCl3, the change detected in electrochemical activity can be related to the transition from localized metal dissolution to crack nucleation; which may involve a redistribution of current over the new crack surfaces. Tests on corrosion fatigue, performed by the authors, were aimed to establish a relationship between Electrochemical Noise and SRET results in order to determine in a semi-quantitative base, the localized corrosion rate and the pit to crack transition process.
FEM analysis corroborated that the local stress conditions for crack initiation in mixed mode, in a semi-elliptic surface pit, overcome the minimum stress level or single threshold stress established from the fatigue limit concept. Superposition ofcyclic shear (ΔKII or ΔKIII> 0) to cyclic tension can lower the mode I threshold stress intensity range, ΔKI, below which crack growth is presumed dominant.
Based on ΔG data, crack initiation will mainly depend on the pit-like crack a/c ratio (α) as well as orientation angle (θ). From theoretical results, it could be assumed that the condition for crack growth initiation at the surface zone (φ = 0˚) are favoured when α ≥ 0.56 and θ ranges from 5˚ to 75º, being the most manifest when θ~45˚.
The alignment of corrosion pit with respect of the direction of applied nominal stress has a strong influence on the conditions for crack initiation. The crack initiation hot points are a function of a/c, θ and φ.
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