Monitoring Tensile Fatigue of Superelastic NiTi Wire in Liquids by Electrochemical Potential
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Fatigue of superelastic NiTi wires was investigated by cyclic tension in simulated biofluid. The state of the surface of the fatigued NiTi wire was monitored by following the evolution of the electrochemical open circuit potential (OCP) together with macroscopic stresses and strains. The ceramic TiO2 oxide layer on the NiTi wire surface cannot withstand the large transformation strain and fractures in the first cycle. Based on the analysis of the results of in situ OCP experiments and SEM observation of cracks, it is claimed that the cycled wire surface develops mechanochemical reactions at the NiTi/liquid interface leading to cumulative generation of hydrogen, uptake of the hydrogen by the NiTi matrix, local loss of the matrix strength, crack transfer into the NiTi matrix, accelerated crack growth, and ultimately to the brittle fracture of the wire. Fatigue degradation is thus claimed to originate from the mechanochemical processes occurring at the excessively deforming surface not from the accumulation of defects due to energy dissipative bulk deformation processes. Ironically, combination of the two exciting properties of NiTi—superelasticity due to martensitic transformation and biocompatibility due to the protective TiO2 surface oxide layer—leads to excessive fatigue damage during cyclic mechanical loading in biofluids.
KeywordsNitinol Shape memory alloy Corrosion Fatigue Tensile test Electrochemistry Hydrogen embrittlement
NiTi-based alloys have established themselves as key shape memory alloy material for wide range of engineering applications  exploiting their unique functional thermomechanical behaviors due to the martensitic transformation driven by the stress and temperature. The key phenomena are the large recoverable superelastic and shape memory strains and strong stress–temperature coupling. When trying to utilize these phenomena in applications designs, NiTi alloys are considered to be exposed to long-time cyclic variations of large stress (<700 MPa), large reversible strains (<7 %), wide range of temperatures (−150 °C to +120 °C), or even corrosive environments (water, blood, biofluids, oil, vapors, hydrogen). Depending on the imposed strain amplitude, the NiTi alloys exhibit thousands to millions of cycles to failure in (thermo)mechanical cycling, no other metallic materials can even approach such a superior fatigue performance at comparable conditions. In successful practical applications, however, the conditions are frequently limited. In this context, the “limited thermomechanical fatigue performance of NiTi” represents an obstacle hindering further development of many engineering applications of NiTi (superelastic stents, orthodontic implants and tools, vibration damping elements, actuator springs, HTSMA actuators).
Fatigue of phase-transforming NiTi has been investigated in the literature both experimentally [2, 3, 4, 5, 6, 7, 8] and theoretically [7, 8]. Although the stress and/or temperature driven martensitic transformation proceeds cyclically in all fatigue tests, fatigue of superelastic medical stents, orthodontic wires and implants, thermomechanical fatigue of actuator wires or springs or fatigue of high temperature actuators seems to be governed by different rules and hence must be dealt with separately.
Functional fatigue (cyclic degradation of functional response)  and structural fatigue  have to be distinguished and possible links between them shall be identified. In spite of the attention paid to the drift of the cyclic stress–strain–temperature responses in the literature [3, 4], it is not still clear how the drift is exactly related to the structural fatigue. There seems to be a general agreement in the literature on a dissipation energy-based fatigue criterion —the more dissipated energy is stored in the material during the transformation cycle, the shorter is the fatigue lifetime. In other words, if there is no energy dissipation, there should be no fatigue and full strain superelastic cycling shall be feasible for millions of cycles. But energy dissipation and hysteresis are intrinsically related to the martensitic transformation and lattice defects are created by phase interfaces propagating during cyclic martensitic transformations . The accumulating defects lead to the microstructure evolution during the thermomechanical cycling  which is believed to control the fatigue performance [3, 6]. But is this really responsible for the experimentally observed preliminary failure of superelastically cycled NiTi? No one proved that yet. Reliable experimental data on the link from the microstructure evolution to the structural fatigue performance of NiTi are still missing. Many researchers, particularly in the community of researchers from NiTi suppliers and medical device companies, believe that the size and shape of nonmetallic inclusions, which cannot deform together with the superelastic NiTi, are primarily responsible for its poor fatigue performance. There are many problems related with the experimental investigation superelastic fatigue of NiTi wire in tension. If the tests are performed at slow strain rates, they are painfully long. At higher strain rates in the air, however, the stress–strain responses are affected by the heat effects , particularly to the latent heat, thermomechanical coupling and heat exchange with the environment. If the fast cyclic loading tests are performed on NiTi wires immersed in fluids, this is not so serious due to much better heat exchange with the fluid, but there is a danger of environmental effects affecting the fatigue performance. The optimum solution for fatigue testing of NiTi wires seems to be mechanical cycling at high frequencies in fluids. Rotating bending fatigue testing on wires  or pulsating fatigue on NiTi stents  is popular in the medical device field. A complication is that the acting surface stresses and strains are not directly measured in rotating bending fatigue tests and interpretation of the results is less straightforward compared to the case of a wire fatigued in cyclic tension.
This work deals with an experimental investigation of structural fatigue of superelastic NiTi wire transforming cyclically in simulated biofluids at constant body temperature under cyclic tension. A motivation comes from our earlier work on fatigue of superelastic NiTi springs cycled in simulated biofluids [13, 14, 15] targeting particularly the problem of unexpected failure of gastrointestinal esophageal, and/or tracheal NiTi stents  braided from NiTi wires or orthodontic wires which are exposed to mechanical loads in corrosive biofluids—i.e., NiTi implants which transform martensitically in the body. Clinical reports of unexpected random failures of implanted braided NiTi stents show that the NiTi wires of implanted stents unexpectedly fractured soon after implantation and the explanted stents exhibited serious embrittlement . Physical origin of the failure remained unclear and corrosion was simply blamed responsible without specifying the exact fatigue damage and failure mechanism.
In a sharp contrast with that, there is vast experimental evidence in the biomedical literature [18, 19, 20] suggesting that carefully engineered TiO2 surface oxide layer on the superelastic NiTi wire separating the liquid environment from the bare metal provides the NiTi with safe protection even against highly corrosive bioenvironments. The TiO2 layer created by furnace oxidation on NiTi consists presumably of mixed polycrystalline anatase with amorphous phase . XPS measurements show excess Ni on top of TiO2 surface (native or heat-treated oxide) in a form of Ni “hut-clusters” (~5 nm) top [22, 23]. The experimentally observed growth of metallic and ionic bonded Ni–O overlayer on the top of TiO2 was explained using the application of the valence bond theory [22, 24].
A question whether the unexpected embrittlement and fracture of implanted NiTi stents shall be ascribed to mechanical fatigue stemming from the bulk or to corrosion attack stemming from the surface was addressed in our recent work [13, 14, 15]. It was concluded that both are probably involved in the gradual fatigue degradation and that cracking of the thin TiO2 oxide layer (grown by thermal oxidation on the wire surface during the shape setting heat treatment) probably plays a key role in the degradation process. The hard ceramic oxide cannot withstand large surface strains due to stress-induced martensitic transformation and fractures when the surface strains exceed 1 % . If the surface oxide does not fracture, the number of cycles to failure quickly increases with the decreasing strain amplitude and reaches a run out number of cycles. It was concluded that the fatigue limit evaluated in NiTi spring tests [13, 15] is controlled by the surface oxide damage. The actual failure mechanism, however, remained unclear.
The presence of the oxide cracks, however, does automatically imply neither degradation of the corrosion properties nor degradation of the fatigue performance of NiTi, though the cracking has been found to result in accelerated Ni release . The oxide layer is too thin to pose any mechanical threat to the wire. Moreover, the damage to the oxide layer caused by the excessive surface deformation gets quickly “repaired” by fast passivation reaction in the biofluid . Nevertheless, NiTi springs superelastically cycled in water and/or biofluids survive only several thousands of tensile cycles (much less than in the air  for the same stroke amplitude) and ultimately fail in a brittle manner. This clearly suggests that the liquid environment does have an adverse effect on the fatigue performance of superelastically cycled NiTi springs. It brought us to the suspicion that chemical reactions proceeding periodically within the cracked surface oxide layer might be responsible for the poor fatigue performance of NiTi wire immersed in biofluid.
Chemical processes at the solid/liquid interface of deforming metals can be conveniently studied by electrochemical methods applied during mechanical loading [26, 27, 28, 29]. In such in situ tests, the deformed metal serves as the working electrode connected in electrochemical cell with inert reference electrode and processes on its surface are tracked down by evaluating electrochemical signals (potential, current, impedance, etc.) during the mechanical loads. These methods were applied in the literature to plastically deformed metals . Mechanochemistry of surface reactions on deformed metals has been explored theoretically . First experiments on NiTi for simultaneous assessment of the electrochemical and structural fatigue properties were designed by Neelakantan et al. .
We have recently performed in situ electrochemical experiments on NiTi wires and springs superelastically cycled in fluids . Basic experiment involves evaluation of the electrochemical Open Circuit Potential/OCP/(potential difference of the working electrode against the reference electrode) during the cyclic tensile loads. The experimentally measured OCP generally depends on the metal, electrolyte, surface layer, temperature, and time of the exposure of the material to the electrolyte. If all this is constant, the experimentally measured changes of the OCP reflect the mechanically induced damage of the surface oxide and the progress of the chemical reactions on the surface triggered by this damage. Potentially very interesting information on the mechanochemical processes occurring on the surface of the fatigued wire can be obtained in this way. In particular, the in-situ recorded OCP signal reflects periodic straining of the surface oxide, cracking of the oxide at large strain amplitudes, crack opening/closing upon tensile cycling or chemical passivation of the mechanically damaged surface.
Physical meaning of the results, particularly how the in situ recorded OCP signals are related to the mechanical data and fatigue performance of NiTi, however, is not clear yet since the method has never been systematically applied to NiTi. This is the main goal of this work.
Superelastic NiTi Wires
Medical grade superelastic NiTi wires were studied in present experiments (Fort Wayne Metals #1, d = 0.2 mm, straight wires with etched, mechanically polished and naturally oxidized surface). The wire samples were prepared from the same batch, given heat treatment in a fluid furnace at 510 °C for 4 min and cooled in water for 3 min. As a result of this treatment, all wire samples used in this study have the same microstructure and same surface oxide as the NiTi spring samples studied in our earlier closely related work [13, 14, 15] (~70 nm TiO2 layer with excess Ni on the top and ~40-nm-thick Ni-enriched layer underneath ). Capillaries were clamped on both ends of the wire sample, electrically isolated with Teflon and epoxy and gripped into the testing rig. All wire samples were 27 mm long and had equal surface area exposed to the electrolyte as the working electrode. All tests were performed on virgin wires.
Electrochemical Testing of Superelastic NiTi Wire Deformed in Liquids
The electrochemical measurements of open circuit potential (OCP), which is also called the corrosion potential (E corr), were performed in a 0.9 % NaCl solution at temperature 37 °C (25, 40, 50 °C) using a GAMRY Reference 600 potentiostat. The acidity of the solution was adjusted to pH = 3 by adding few drops of dilute HCl in order to simulate physiological and corrosive environment the medical stents are exposed to.
The volume of the solution in the electrochemical cell was 130 ml. Potentials were measured against a reference silver chloride electrode (Ag/AgCl, −0.025 V vs SCE). The surface area of the thin NiTi wire acting as the working electrode was as small as 0.170 cm2. This lead to very low electrochemical current, suppression of capacitive currents and ensured non-polarizability of the reference electrode. The distance between the reference and working electrode was less than 1 mm. There was no need to use IR compensation.
The OCP value measured in the in situ electrochemical test on NiTi wire acting as the working electrode in the electrochemical cell thus characterizes an electrochemical quasiequilibrium at the NiTi/liquid interface reflecting the kinetics of both half-cell reactions. When this equilibrium is changed by the mechanical deformation of the NiTi surface, the kinetics of chemical reactions changes and the experimentally measured OCP reflects this change and evolves in time. Increase of the OCP in time evidences progress of the oxidation process (Eq. 1), while decrease suggests prevailing reduction process (Eq. 2) at the NiTi/liquid interface.
In Situ Electrochemical Testing During Tensile Cycling of Superelastic NiTi Wire
Two types of in situ electrochemical tests were performed: (a) kinetics experiments on deformed NiTi wires and (b) cyclic experiments. In the kinetics experiments, the wires were strained (unloaded) in the liquid up to a preset strain level using defined strain rate, while the OCP response was evaluated during the straining and predefined period of time afterwards. In the cyclic experiments, the wires were subjected to cyclic tensile tests characterized by test parameters as e.g., mean strain, strain amplitude, strain rate, temperature and the OCP response was continuously evaluated during the cycling.
As introduced above, the experimentally recorded OCP signal reflects mechanically induced local breakdown of the passive oxide layers triggering the chemical reactions on the wire surface. Note that the oxide damage is brought about by the excessive superelastic deformation caused by the stress-induced MT in the NiTi matrix underneath the oxide. While the damage to the oxide layer caused by the NiTi deformation is instantaneous, the progress of chemical reaction (Eqs. 1, 2) is delayed. The surface strains vary periodically during the cyclic tensile tests, unfortunately the localized deformation of NiTi in tension complicates the issue significantly.
The in situ recorded OCP signal was stored together with external force, elongation and temperature. The OCP sampling rate in kinetics tests was set at 1000 Hz. High sampling rate is essential to evaluate the minimum value of OCP established as a result of deformation-induced damage followed by very fast passivation of NiTi wire. The OCP minimum approaches the true corrosion potential of the bare NiTi alloy exposed to electrolyte.
Characterization of the Cracked Surface Oxide by SEM
SEM/FIB techniques were employed to characterize the surface defects introduced by the cyclic tensile deformation. SEM observation was performed using FIB/SEM TESCAN FERA3 electron microscope on the NiTi wire sample, which was previously subjected to the tensile fatigue test (strain rate = 1 % s−1, simulated biofluid, T = 37 °C, N F = 1500). The wire was stretched using a special tensile holder to 6 % strain. A part of the wire was still in austenite structure with closed surface oxide cracks (~1 % strain), while the majority of the wire was in the martensite shearband (~7 % strain) with surface oxide cracks open. Subsequently, cross sections were cut through the wire in areas of interest using the FIB with Ga+ ions using the TESCAN LYRA SEM perpendicularly to the major oxide cracks. Final polishing was carried out using current of 560 pA and cracks penetrating into the NiTi matrix were studied on the polished cross sections. Finally, 3D reconstruction of subsurface distribution of microcracks was performed using cross-sectioning method by automated FIB milling combined with SE scanning of the bulk 40 × 10 × 17 μm (400 slices in steps of 100 nm).
Cyclic Tensile Deformation of Superelastic NiTi Wire in Biofluid and in the Air
The essential point is that the number of cycles till failure is significantly lower in the liquid than in the air. In the small amplitude range, the NiTi wire survived 100 mil. cycles at strain amplitude 0.5 % while only N f = 4000 cycles in biofluid. This suggests that the fatigue limit is different in the liquid and in the air. We did not perform sufficient number of tests at different stress amplitudes to construct Wohler curves, but we made enough tests to learn that the experimental results under given test conditions (strain amplitude, mean strain, strain rate, temperature, environment) are reproducible with a very small scatter ΔN f < 5 %. This is due to the fact that all samples have same microstructure, same surface oxide and particularly that all tests are performed in thermally controlled chamber (air or liquid) isolated from the surrounding environment. The fact that number of cycles till failure is lower in the biofluid than in the air turned our attention towards the surface Ti02 oxide, as already explained in the introduction. We started to doubt whether the evolution of the bulk microstructure, which is responsible for drift of the cyclic stress–strain curve upon cycling (Fig. 3c), has a decisive impact on the fatigue lifetime of NiTi wires cycled in biofluid. In other words, we started to suspect that the fatigue damage originates from the mechanochemical processes at the wire surface, as common for the environmentally assisted fatigue. Hence, we decided to monitor the accumulation of the surface damage during tensile cycling by employing the in situ OCP method.
OCP Kinetics Tests on Strained NiTi Wires
Regardless of the applied strain, the OCP of the deformed wire increases in the long run (~3600 s) up to starting level in all kinetics tests, similarly as shown in Fig. 4a. It shall be noted that, except the lowest applied strains, the NiTi wire is exposed to the liquid in partially martensitic state with the surface oxide cracks opened. The surface oxide is yet virgin (uncracked) in the rest of the wire, though homogeneously strained to about 1 % due to the external stress applied in the kinetics test. Please note that, as a consequence of the strain localization in shear bands, the oxide cracks on top of the shear band are kept in opened state by the surface strain ~7 %, regardless of the actual magnitude of the applied strain.
As the experimentally measured evolution of the OCP is an integral value from the whole wire, modeling has to be employed to interpret the meaning of the in situ OCP experimental data in view of the actual processes occurring at the wire surface upon straining. This exceeds the scope of this work. Here, the aim was mainly to overview what kind of in situ OCP information can be obtained from the kinetics tests.
It was found that, by following the evolution of the OCP of the wire subjected to straining, we can detect the mechanically induced damage to the surface layer as well as the progress of the subsequent chemical reactions. The chemical reactions proceed extremely fast once the surface oxide damage occurs and continue to proceed with gradually slowing down rate. Studying their kinetics in detail is essential for cyclic superelastic fatigue of NiTi wires, since the progress of the periodical surface oxide damage and passivation during tensile cycling cannot be understood without understanding the kinetics of the mechanically triggered chemical reactions.
In Situ OCP Experiments During Cyclic Tensile Loading
With this knowledge from kinetics tests, let us proceed to the in situ OCP studies of NiTi wire subjected to tensile cycling, where the damage and passivation processes occur periodically. The key point is that superelastic strains as large as 8 % are reversible in cyclic tensile tests and the same of course is the case for surface strains. This means that reversible surface strains as large as 8 % occur repeatedly during the cyclic tensile test. Not only the oxide layer fractures but also the subsurface layer of the NiTi matrix is periodically stressed, strained, and martensitically transformed from the austenite to martensite. All this potentially affects the mechanochemical processes at the wire surface.
Due to the nonlinear hysteretic character of the superelastic stress–strain response of NiTi, we make a distinction between the elastic deformation in austenite state at small strains (Δε < 1 %, “Cyclic Loading in Austenite Elastic Range” section), and superelastic deformation at larger strains (Δε = 1–7 %, “Superelastic Cycling Involving Stress Induced Martensitic Transformation” section). Further on, we investigate the effect of strain rate, mean strain, strain amplitude, and temperature on fatigue performance. Let us, finally, note that the in situ OCP method is noninvasive in electrochemical sense.
Cyclic Loading in Austenite Elastic Range
There are significant differences between the OCP responses of NiTi and tungsten. Neglecting the very different OCP values for both wires, which is most likely due to different surface oxides and different electrochemical reactions, main difference is that the NiTi shows much larger OCP variation during single cycle. Since the damage prevails over passivation in the first 30 cycles, the OCP gradually decreases upon cycling. Later on, however, the situation reverses and OCP gradually increases.
Superelastic Cycling Involving Stress-Induced Martensitic Transformation
It shall be pointed out that, although the OCP value gradually increases upon cycling, the average value of the cycled wire remains low (<−200 mV) compared to that of the static NiTi wire (~−50 mV). The superelastically cycled NiTi wire in simulated biofluid is thus exposed for most of the lifetime to much more negative electrochemical potential than the static or elastically cycled NiTi wire.
Effect of Strain Rate
These results suggest that the passivation of the surface damage is less effective when the cyclic test is carried out with higher strain rate. It might have an impact on the number of cycles till failure, on the other hand, the higher transformation stress at higher strain rates might affect the fatigue performance of the wire as well.
Effects of Mean Strain and Strain Amplitude
The number of cycles till failure is largest (N F = 16,000) when the test is performed at largest mean strain 7.5 % in the martensite state and smallest (N F = 1050) for the mean strain in the transformation range at 4 %. This is very surprising taking into account that the stress applied during the tensile cycling in the martensitic state is by far highest (Fig. 14b). These tests were performed 3 times and the results are very well reproducible. The fatigue performance of the wire fatigued at the mean strain 4 %, where the shear band front moves, is worst.
Effect of Temperature
Damage Accumulation, Strength, and Failure
In view of this, the correlation of the OCP evolution with the degradation of the strength of the cycled NiTi wire was investigated (Fig. 18). When the OCP reached maximum (S1) or entered the decreasing stage beyond the maximum (S2, S3), the cyclic tests were stopped and the wires were loaded in tension up to the fracture. It was found that the strength did not change with the increasing number of cycles for most of the fatigue lifetime. After the OCP approached the maximum, the strength decreased rapidly (Fig. 18a, c). This shows that the OCP decreasing after reaching the maximum correlates with the rapid deterioration of the strength of the wire.
This confirms that the accelerated growth of fatigue cracks into the NiTi matrix is indeed related to the OCP decrease. The OCP is very sensitive to the surface damage. Because of that, it heralds the upcoming wire fracture even if the stress–strain–electrical resistance response fails in that respect.
No detachment of the oxide layer, oxide flaking, or any other oxide damage induced by tensile cycling was ever observed.
An appealing question was whether the tiny oxide cracks serve as nucleation sites for fatigue cracks growing later upon cycling into the NiTi matrix. To find an answer, FIB cross sections perpendicularly to the larger cracks were observed by SEM (Fig. 20c–e). A dense array of short matrix cracks (typically 100–300 nm long and ~500 nm separated) was observed on the cross sections right under the surface oxide layer. Major cracks growing several microns deep into the NiTi bulk were observed underneath the major surface cracks. A one-to-one correlation between the tiny oxide cracks and short matrix cracks was clearly confirmed (Fig. 22). The cracks were also studied in detail by 3D reconstruction technique by automated FIB milling combined with SE scanning. The results will be reported separately.
Corrosion properties of NiTi immersed in biofluids have been studied since the very beginning of the development of superelastic technologies. Overwhelming literature evidence supports the view that carefully engineered Ti02 surface oxide layer provides excellent protection to static NiTi implants immersed in biofluids [18, 19, 20] and reasonable protection to NiTi implants deforming elastically in biofluids [12, 19]. The results presented above suggest that the situation might be very different in case of NiTi implants that deform superelastically in body fluids.
Cracked Ti02 Oxide
When NiTi deforms superelastically in liquids, the ceramic oxide layer on its surface cannot withstand the large superelastic strain accompanying propagation of the shear band and fractures in the very first tensile cycle (Fig. 1). Following that, the surface oxide contains array of regularly spaced nanocracks arranged perpendicularly to the wire axis. The surface of superelastically cycled NiTi wire is thus covered not by the surface oxide but by the “cracked surface oxide.” The density (separation) of the oxide cracks is assumed to correlate with the plateau strain, though no specific investigations were carried out.
When shear band transformation proceeds in the cyclic superelastic tensile test, the surface deformation changes periodically from ~1 to ~7 % at the moving shear band front. The damage of the already cracked surface oxide layer upon cycling is assumed to be limited to the existing oxide cracks. The stress in the oxide areas among the existing cracks is expected to be lower than it was at the peak elastic stress in the first cycle, which is why it does not fracture anymore upon tensile cycling and why the small cracks (length, density) look similar after the 1st cycle and 1500th cycle. The damage introduced into the surface in each superelastic cycle is thus assumed to be localized into the tips of the existing oxide cracks.
Although, the actual chemical reactions occurring at the fresh surface of reactor steel and NiTi are different, similar approach is currently being developed for environmental fatigue of NiTi, taking into account the strain reversibility—i.e., that the activated area fraction A* is up to some extent reversible upon unloading. The results will be reported separately.
Mechanochemical Reactions at the NiTi Surface
In reality, the TiO2 surface oxide is never ideal, there are inhomogeneities, notches, inclusions, etc., where the chemical reactions do proceed and hence the OCP is different from zero. Since the negative potentials prevail in case of the NiTi, cathodic current dominates the cell current and hence OCP levels typically approach slightly negative values (~−50 mV in case of heat-treated NiTi with thicker oxide (Fig. 21b) and ~−200 mV in case of mechanically polished NiTi wire with thinner oxide). Note that there is an anomaly on the Potentiodynamic polarization curve of the oxide-free wire around 0 mV (Fig. 21a). This is assumed to be due to the massive oxidation reaction taking place upon increasing the potential in the test on the mechanically polished wire in which the reactions are controlled by the externally applied potential.
The stable electrochemical situation at the passivated surface of the NiTi wire immersed for about an hour changes dramatically when the surface oxide is mechanically damaged by loading the wire and the electrolyte comes into contact with the bare NiTi surface. Even slightest deformation of the metal may introduce nanocracks into the brittle surface oxide which instantaneously affects the chemical reactions (Eqs. 1, 2), particularly, the anodic reaction (Eq. 1) massively releases free electrons into the NiTi metal and shifts the potential of the NiTi alloy to more negative values in response to the damage. The electrochemical cell reacts by instantaneous change of the OCP potential to more negative values. The negative potential in turn slows down the anodic reaction and speeds up the cathodic reaction (passivation), which is the reduction of hydrogen ions H+ giving rise to atomic hydrogen. As a result, the OCP increases back to the more positive (noble) values.
This would be the general scenario. NiTi, however, is somehow special. Separately, both Ni and Ti have different electrochemical behaviors. According to the nobility classification of metals , Ni is more noble than Ti (Fig. 21a). However, equiatomic NiTi alloy, similarly as Ti, forms protective titanium oxides (Fig. 21b) which provide these metals with excellent protective passivation ability in contact with aggressive environments. In chemical terms, titanium is passivated by galvanic coupling with nickel. If cathode (Ti) and anode (Ni) area ratio is 1:1, exchange current dramatically decreases. The mixed potential of the Ni–Ti galvanic couple is thus even more noble than that of the Ti (Fig. 21a). Hence, NiTi alloys immersed in liquid environments with the concentration of H+ are even more easily passivable than the unalloyed Ti and belong, because of this, among the noblest metals.
Hydrogen Uptake and Transport by the Cyclically Deformed NiTi
Because of the high values of its diffusion coefficient, hydrogen can relatively easily move through the NiTi lattice even at 37 °C and just as easily be removed from it . As the diameter of a hydrogen atom is very small, it occupies the interstitial sites at room temperature. As in other titanium alloys, hydrogen in NiTi also tends to form titanium hydrides . Since the specific volume of titanium hydride is larger compared to that of the NiTi lattice, stress concentrations arise around it. NiTi can be hydrogenated either by exposing it to hydrogen atmosphere at high temperatures or by charging it electrolytically at room temperature. Virgin TiO2 layer prevents hydrogen from entering the NiTi from the electrolyte. When the surface oxide fractures, NiTi can be hydrogenated electrolytically even more easily. The hydrogen absorbed by the NiTi, however, suppresses the martensitic transformation . In superelastically transforming NiTi, suppression of the transformation inevitably leads to the increase of the local stress, plasticity or possibly even to cracking. According to the literature , the effect of absorbed interstitial hydrogen on the kinetics of dislocation and transformation processes is confined to a narrow temperature and strain rate windows, outside of which, solute hydrogen can have very different, even opposite effects.
Yokoyama and coworkers systematically investigated embrittlement of hydrogenated NiTi (see [38, 39, 40] and references there). They hydrogenated NiTi both by exposing it to gaseous hydrogen at high temperatures and by the electrolytic route to find out that the adsorbed hydrogen brings about severe decrease of the strength [37, 38] and leads to brittle fracture [38, 41]. Particularly, they claimed that the hydrogen adsorption rate is much faster, when the NiTi is electrolytically hydrogenated while it transforms during cyclic mechanical loads , compared to the cases when it is stress free, under constant stress or cyclically loaded in elastic range.
Although the actual mechanism of the hydrogen embrittlement of NiTi needs to be investigated further, there should be no doubt that both the suppression of the martensitic transformation  and the formation of Ti hydrides  would lead to the acceleration of the crack growth and promotion of brittle fracture of superelastically cycled NiTi. However, this is the case for the intentionally hydrogenated NiTi. The hydrogen-free NiTi immersed in biofluids should be perfectly safe from the hydrogen embrittlement, as generally argued in the literature [18, 19, 20, 42].
At the same time, when the NiTi wire is exposed to the biofluid for a long time, as is the case of medical implants, it is possible that the corrosive chemical processes proceeding for a long time may decrease the strength of the NiTi wire. Inspection of the fractured wire segments from explanted esophageal NiTi stents reported in the literature [16, 17] confirm significant corrosion damage. This apparently supported the widespread view within the community that corrosion has to be taken seriously as the possible origin of the apparently random NiTi fractures. We have performed a series of long-time immersion tests, in which this NiTi wire was exposed to various simulated biofluids in virgin state as well as in deformed state (wire was wound around 2 mm plastic bar) for up to 72 days. No effect of the long-time immersion on strength and functional properties of the NiTi wire was found at all. This excluded possible effect of the chemical attack during the long-term corrosion on the strength even for immersed NiTi wire, including the wire with cracked surface oxide and stress-induced martensite in the subsurface matrix.
As introduced in the section “Mechanochemical reactions at the NiTi surface,” hydrogen is produced by the mechanically driven chemical reactions (5, 6) triggered by the electrolyte coming into contact with the bare NiTi within the oxide cracks as suggested in Fig. 22. The oxide/NiTi matrix interface was investigated by atomistic modeling in Ref. . An interesting structural relaxation giving rise to a columnar structure in which alternating long and short Ni–Ti bonds are present in each surface and subsurface plane is reported. A thermodynamic analysis suggested that the most stable interface structure is that with Ti vacancies in the NiTi surface. This is in perfect agreement with frequent literature evidence [14, 18] for Ni-rich layer in the subsurface NiTi matrix.
Such oxide/alloy interface structure would be relatively open for hydrogen adsorption. The solubility of hydrogen in liquids is greater at low temperatures . Both adsorption and dissociative chemisorption of hydrogen accompanying the crack growth suggested in Fig. 22 depend on hydrogen charging conditions, temperature, and mechanical loading, which cannot be understood without performing dedicated experiments.
The mechanically driven chemical reactions (5, 6), however, can only lead to the hydrogen embrittlement, if sufficient amount of hydrogen is generated at the surface and if this hydrogen diffuses into the bulk at the 37 °C temperature. Due to the strong potential dependence, extreme hydrogen concentrations can be accommodated just underneath the surface . Concerning the hydrogen diffusion in the NiTi matrix, martensitic phase transformation makes the assessment complicated. It is well known that atomic hydrogen in metals tends to be concentrated in the so-called “hydrogen traps.” Most of the structural inhomogeneities, as grain boundaries or dislocations, act as hydrogen traps. The hydrogen trapping might be reversible or irreversible, depending on whether the trapped hydrogen is easily released or tightly bounded. From this point of view, nano-sized partially recrystallized microstructure of heavily cold-worked medical grade NiTi wires  with its grain boundaries, defects, and internal stresses should absorb hydrogen more easily than the fully annealed NiTi. Martensite with internal twins and variant interfaces should be theoretically even more open for hydrogen diffusion than the austenite phase.
Additionally, the phase-transforming NiTi contains high density of moving phase interfaces that generate slip dislocations during cyclic mechanical loadings [9, 10]. Assuming that the hydrogen diffuses along the core of the dislocations within the moving interfaces , one can imagine a very efficient hydrogen transport from the surface to the bulk along the paths, where the interfaces repeatedly move during the cyclic superelastic deformation. Such mechanism would explain the experimental results of Yokoyama et al. [39, 40]. Considering that the adsorbed hydrogen locally suppresses the martensitic transformation [35, 41, 46], one can deduce that the local internal stress necessary to drive martensitic transformation in the hydrogenated areas gradually increases with the increasing hydrogen content. Eventually, the crystal lattice might locally stop to deform superelastically, which would accelerate propagation of cracks in the hydrogenated areas (Fig. 22). Similarly hydrides and hydrogen traps would benefit crack growth (Fig. 22 right).
Since the hydrogen is produced only during the short time after the oxide damage event when the electrolyte reaches the bare NiTi surface, it is evident that the surface oxide damage must occur repeatedly in a cyclic manner in order to assure sufficient hydrogen production. At the same time, very efficient hydrogen transport to the bulk will be assured by the periodically moving phase interfaces and dislocations, as introduced above. Hydrogen transport by periodically moving interfaces and dislocations leads to enhanced hydrogen concentrations at inhomogeneities as grain boundaries or inclusions, where hydrogen traps form. Both conditions are ideally fulfilled in parts of the wire, where shear band fronts periodically move upon tensile cycling.
The periodical oxide damage is localized at the crack tips (Figs. 1, 22, 23), while the uncracked oxide areas among the cracks probably passivate continuously upon cycling, equally as the areas unreached by the moving shear band fronts. Because of this, the opening/closing oxide cracks under the moving shear band fronts are assumed to be the locations of preferential hydrogen production, the matrix cracks are assumed to be initiated there and this is where the wire ultimately fractures, when major cracks develop and grow deep into the matrix.
Mechanochemical Reactions upon Cycling Evidenced by the In Situ OCP
As the shear band front(s) move forward and back during the cyclic superelastic tensile loading, the surface oxide cracks open/close in a response to the surface strain varying from 1 to 7 %. While the strain increases, fresh new bare NiTi surface becomes periodically exposed to the electrolyte (Figs. 1, 20, 22, 23). The experimentally measured OCP provides information about the chemical processes triggered by the mechanical damage at the surface. Although the OCP starts to decrease already in the elastic range before the shear band is nucleated (Figs. 4, 5, 6, 7, 8), major drop of the OCP is related to shear band nucleation and consequent oxide cracking. The NiTi surface, however, has intrinsic ability to recover the mechanically induced damage by the passivation (chemical reaction 5) pushing the OCP to higher values and restoring thus the electrochemical equilibrium at the solid/liquid interface. This scenario was deduced from the analysis of the results of the kinetics tests (Figs. 4, 5, 6, 7, 8). When the wire was deformed till elastic strains only, the surface oxide was deformed elastically but not broken. OCP decreased in response to the cyclic straining. This probably introduced into the oxide layer a homogeneously distributed damage but not the cracks. There was no sharp OCP minimum since there was no subsequent passivation after the damage (see kinetics tests in Figs. 6a, 7a). The existence of the OCP minimum on OCP–time curves recorded in kinetics tests up to larger applied strains is thus considered to be related to the massive oxide cracking accompanying the shear band nucleation. Once the surface oxide fractures and the bare NiTi surface is suddenly exposed to the electrolyte, OCP sharply fells but, at the same time, the passivation reaction starts pushing the OCP up again. The increase of the OCP [lasts only for ~250 ms in the fast kinetics tests (Fig. 7)] thus evidences the massive oxidation taking place at the bare metal surface at the opened crack tips. When the tensile deformation is imposed slowly (Fig. 6) in the kinetics test, the situation is more complex due to the overlapping kinetics of the reactions proceeding in various locations on the nonhomogeneously deforming wire surface. The oxidation reaction occurs already, while the wire is being deformed and short time after that (~250 ms) (Fig. 6c, d). Recall that the oxidation reaction is responsible for the hydrogen generation. The mechanically driven chemical reactions thus effectively work as a kind of “pump supplying atomic hydrogen to NiTi,” as introduced in “Mechanochemical reactions at the NiTi surface” section.
Since the oxidation processes are inhomogeneously distributed over the surface of the inhomogeneously deforming wire, the OCP kinetics curves (Figs. 4, 5, 6, 7) can only be interpreted via dedicated modeling based on the kinetics Eq. 4. The overlapping damage and passivation during the kinetics tests also rationalizes the experimentally observed dependence of the value of the OCP minimum on the imposed strain and strain rate (Fig. 8). The results of the modeling of the kinetics tests are going to be reported in a separate article.
Selected results concerning cyclic elastic loading of the NiTi wire in austenite state, where the surface damage is supposed to be homogeneous, are shown in Fig. 9a, b. Based on the gradual decrease of the OCP in the first 30 cycles (Fig. 9b), it can be deduced that the damage is introduced into the oxide layer gradually (Fig. 23 top). The OCP starts to increase when the passivation reaction prevails over the damage. The NiTi wire exhibits much stronger tendency for the passivation than the Tungsten wire. Although this is very interesting, we will not pay further attention to the cyclic loading of NiTi in the elastic range, since this article focusses on the superelastic fatigue.
As introduced above, the essential problem for the analysis of the OCP recorded during the superelastic cycling is that the experimentally recorded evolution of the OCP reflects the progress of mechanochemical reactions integrated over the whole surface of the wire but the shear band nucleation and propagation during the superelastic deformation are strongly localized in space and the shear band front(s) move. The evolution of the OCP recorded during the superelastic test (Figs. 10, 11) is thus very different from that observed in the elastic loading test where the deformation is homogeneous. The OCP fells to a deep minimum during the first forward tensile loading and then gradually increases upon further cycling (Figs. 10c, 11a). Since the experimentally measured OCP is an integrated value over the whole wire surface, one cannot directly deduce what happens at the propagating shear band front (Fig. 1) from the experimentally recorded OCP–strain response during a single cycle (Fig. 11a). Dedicated modeling of the nonhomogeneous and time-dependent damage and passivation is again needed. In particular, even if we do not see any sharp OCP minimum on the OCP–strain curve, we anticipate that the oxide damage followed by passivation events (Eqs. 4, 5, 6) proceeds locally at the propagating shear band front and that this repeats during the tensile cycling. As the passivation reaction tends to dominate over the damage from the second cycle, the average OCP gradually increases upon cycling.
The surface of the NiTi wire subjected to superelastic cycling is thus exposed to the periodical sequence of the breakdown/passivation events. The essential point is that, within the periodically opening/closing oxide cracks (Fig. 23 middle), the bare NiTi matrix is repeatedly exposed to the biofluid which triggers the chemical reactions (Eqs. 5, 6) leading to hydrogen generation, as introduced in “Mechanochemical reactions at the NiTi surface” section. To confirm this role of the hydrogen, we applied negative electrochemical potential of ~−700 mV during the superelastic fatigue test. This promoted the activity of the chemical reaction (5) which accelerated the hydrogen generation upon the tensile cycling. As a result, the number of cycles till failure was reduced to ~600.
The Effect of Test Parameters on Fatigue Performance
The results of the systematic investigation of the effect of various test parameters (strain rate (Figs. 12, 13), mean strain (Fig. 14), strain amplitude (Fig. 15), and temperature [Figs. 16, 17)] on fatigue performance show that there is a correlation between the in situ evaluated OCP and number of cycles till failure. Some of the results as discussed below are intriguing.
Very surprising is the fatigue performance of the wire improving with the increasing mean strain (Fig. 14). The number of cycles till failure in case of the 7.5 % mean strain is about 15 times larger than for the mean strain 4 % and this is very reproducible. How can it be? Recall that in case of 0.5 % mean strain and 7.5 % mean strain, there are no shear bands and the deformation is homogeneous. In case of the 0.5 % mean strain, the wire is cycled in austenite elastic range and the OCP decreases gradually upon cycling (Fig. 14c). The damage is thus expected to prevail over passivation till ~30th cycle (Fig. 23 top), when the passivation starts to prevail and OCP starts to increase. In case of the mean strain 4 %, the situation is very different. The shear band front(s) somewhere in the wire (Fig. 1) move very little in response to the externally imposed small strain amplitude, as can be deduced from the marginal stress hysteresis observed in Fig. 14b. Although the damage is localized into the very narrow region, where the shear band front(s) move, it results in lower OCP recorded in the 100th cycle (Fig. 14b). The highest OCP value observed in case of the mean strain 7.5 % can be rationalized by assuming that passivation reaction in the widely opened crack (Fig. 23 bottom) leads to accumulation of the TiO2 gel at the crack tip and steady increase of the OCP upon cycling. The bare NiTi surface is not directly exposed to the electrolyte in case of the mean strain 7.5 %, as a result of which the generation of hydrogen is minimal and fatigue performance dramatically improves in spite of largest strain and stress.
In addition, the above introduced “hydrogen pump” works homogeneously over the wire surface and the surface strain variations are rather small (<1 %) in case of the mean strain 0.5 and 7.5 %. But in the case of the 4 % mean strain, hydrogen generation concentrates into the surface areas, where shear band front(s) move (Fig. 1) and the local surface strain variations are large (~6 %). The localized hydrogen generation at the moving shear band front is much more effective since the strain is large. This is the key argument explaining the shortest lifetime observed in case of the 4 % mean strain. Second argument, however, is the already mentioned fast hydrogen transport by the moving interfaces which is obviously active only in case of the 4 % mean strain. Even if the “hydrogen pump” would produce same amount of hydrogen per cycle for all three mean strains, building upon this argument, the hydrogen would be fastest adsorbed and transported into the bulk in case of the 4 % mean strain. Due to the hydrogen-induced loss of the strength, the number of cycles till failure would be lowest in this case. Third argument for the shortest lifetime of the wire cycled at the 4 % mean strain is based on the concentration of stress in location where the shear band front intersects with the wire surface. We have recently evaluated the topology of the shear band front and stresses around it experimentally by performing a unique 3D XRD experiment on thin NiTi wire stretched in tension . It shall be mentioned that the increasing number of cycles till failure with the increasing mean strain was already reported in the literature before, e.g., by Pelton et al. , who performed fatigue tests on stent-like V-shape specimens processed from Nitinol microtubing. Since there are no shear bands in case of the V-shape samples, the observation of better fatigue performance of NiTi at larger mean strains in the martensite state in yet some other studies  might be of general relevance.
The increase of number of cycles till failure with the increasing strain amplitude (Fig. 15) is even more curious. Although this is ridiculous from the point of view of conventional fatigue behaviors of metals, it is perfectly understandable in the context of the hydrogen embrittlement due to mechanically driven chemical reactions on the surface of NiTi wire deforming via shear band front propagation. To break the wire, there is no need to make it brittle everywhere along its length, it is enough if this occurs in places where the shear band front moves. The larger is the strain amplitude, the less negative is the OCP (Fig. 15b), meaning that the passivation is more effective. As the strain amplitude gets smaller, the “hydrogen pump” operates efficiently only in the part of the surface swept periodically by the moving shear band front(s). Since the OCP continuously increases in the rest of the wire surface, the integral OCP eventually becomes least negative in case of the smallest strain amplitude. Locally, however, in the part of the wire regularly swept by the moving shear band front(s), the mechanochemical reaction might work even more efficiently at smaller strain amplitudes, since there is little time left for the passivation. The second argument (the hydrogen uptake by phase-transforming wire) and third argument (the increased stress at the shear band front) proposed in the previous paragraph would favor the increasing fatigue lifetime with the increasing strain amplitude as well. It comes out, that to assess the fatigue performance of superelastic NiTi wire in cyclic tension, it is very useful to plot fatigue limit in the mean strain–strain amplitude space, as proposed by Pelton et al. . We did not do it since we did not have enough data points.
The number of cycles till failure decreasing with the increasing strain rate (Figs. 12, 13) is not common as well. The effect is, however, relatively small. The decrease of the OCP with the increasing strain rate (Figs. 12a, 13) is evident. Since the passivation is a time-dependent process, there is simply less time for it in tests performed with higher strain rates. Whether this is directly related to the decreasing number of cycles till failure or not is, however, questionable. The strain rate also affects the superelastic response (Fig. 13) and its evolution upon cycling (Fig. 12d). The higher transformation stress at higher strain rates most likely originates from the impact of the latent heat effects on superelasticity  and fatigue performance might worsen with the increasing stress (Fig. 12d).
Finally, the increasing temperature has negligible effect on the in situ recorded OCP (Figs. 16, 17) suggesting that the effect of temperature on the mechanochemical reactions at the surface is marginal. The number of cycles till failure, nevertheless, decreases with the increasing temperature. The decrease of the fatigue lifetime with the increasing temperature might be due to the transformation stress increasing with the increasing temperature.
Damage Accumulation and Fracture
What is it actually the “damage” evidenced by the sharply decreasing OCP? Neglecting the early elastic range, where it could be related to the stresses in the surface oxide, the damage consists mainly in the oxide cracking. Later, when cracks appear at the surface and grow into the NiTi matrix, the oxide gel at the crack tip is disrupted by the straining and exposes the bare metal to the liquid again and again (Figs. 22, 23). In this respect, major damage occurs in the first superelastic cycle when the virgin oxide is firstly broken into the cracked oxide layer with millions of nanometer-sized cracks (Fig. 1).
The oxide cracks periodically open/close upon tensile cycling (Figs. 19, 20) and the damage/passivation events (Figs. 22, 23) are localized there. The SEM observation of the small cracks on the surface showing one-to-one correspondence with the small cracks observed on cross section of the fatigued wire (Fig. 22) clearly supports that view. The fact that the OCP increases during superelastic tests suggests that the surface damage is in fact gradually “cured” in spite of the cyclic mechanical loading. The real irreversible damage, however, cannot be detected by the surface SEM observations, since it consists in the local hydrogen embrittlement of the NiTi matrix underneath the oxide cracks enabled by the mechanochemical reactions, nucleation of matrix cracks, and their growth in the embrittled NiTi lattice.
In addition, there are those major cracks appearing frequently at inclusions and notches on the surface of the fatigued wire (Fig. 19), which penetrate several microns deep into the NiTi matrix (Fig. 20). This can be readily understood based on the fact that the hard elastic inclusions that cannot deform together with the superelastic NiTi matrix act as natural stress concentrators. On top of that, it is likely that the hydrogen adsorption can be accelerated at the oxide or carbide inclusions on the surface (Fig. 19) and that the inclusions thus act as a kind of “surface hydrogen traps.” This would explain why major cracks, the propagation of which leads to the fracture, are frequently connected to the surface inclusions in view of the hereabout introduced mechanism.
fracture of the TiO2 surface layer by dense network of thin oxide cracks,
periodical opening/closing of the oxide cracks exposing the bare NiTi repeatedly to the electrolyte,
hydrogen generation by the mechanochemical reaction (passivation) at the NiTi/liquid interface,
uptake of the atomic hydrogen by the bare NiTi surface,
transport of the hydrogen into bulk NiTi enhanced by the periodically moving phase interfaces during the cyclic martensitic transformation,
local loss of the strength of the NiTi matrix due to the hydrogen embrittlement and suppression of martensitic transformation,
transfer of the oxide cracks into the embrittled NiTi matrix,
propagation of selected cracks along the hydrogen traps causing ultimately the brittle fracture of the wire.
Ironically, combination of the two exciting properties of NiTi—superelasticity due to martensitic transformation and biocompatibility due to TiO2 surface oxide layer—thus leads to accelerated fatigue damage during cyclic loading in biofluids. The hydrogen-based fatigue degradation mechanism is proposed especially for NiTi, other SMAs, as e.g., Ti–Nb–Ta or Ti–Nb–Zr medical alloys might behave differently as recent electrochemical studies  show. A question remains whether the mechanism may also operate in atmospheric moisture.
The essential point is that the mechanism originates from the surface not from the microstructure evolution in the bulk, though the bulk deformation processes play significant role in it, since they allow for the excessive surface deformation and for the hydrogen transport. The mechanism might potentially pose a threat for any low modulus Ti alloy-based implants covered by Ti oxides. However, note that medical implants designed as a “structural elements” undergo much smaller surface strains than the thin NiTi wire and that the cyclic martensitic transformation required in step v is missing. Another likely consequence of the mechanochemical reactions during the superelastic cycling of NiTi wires immersed in biofluids is presumably a drastic increase of the Ni release from the cycled wire compared to the static NiTi wire (virgin or deformed  ). This shall be taken as a prediction that should be verified by dedicated experiments.
It shall be mentioned that the local hydrogenation and consequent decrease of the strength of NiTi due to the cyclic superelastic deformation in fluids is not the same as the homogeneous hydrogenation of NiTi by conventional means [38, 39, 40, 41, 42, 46, 49, 50]. Minor homogeneous absorption of hydrogen by NiTi does not have to necessarily decrease its strength. It may have even beneficial effect on, e.g., corrosion  or damping properties . Hydrogenated NiTi recovers its strength upon long-time aging even at room temperature .
Finally, it shall be pointed out that fatigue performance of the thin NiTi wires in cyclic tensile tests depends critically on the type and quality of the oxide layer resulting from the surface finishing treatment. NiTi wires with different oxide layers exhibit very different number of cycles till failure. Recall that all samples studied in this work had exactly the same surface oxide layer achieved by the same heat treatment. We shall admit that this particular oxide layer  definitely did not provide the wire with the best fatigue performance. But this is not considered to be an issue here, since the goal of this work was to reveal the degradation mechanism and to develop a method that can be used to evaluate various surface finishing treatments of NiTi wires in view of the best superelastic fatigue performance in simulated body fluids. Fatigue testing of NiTi wires having same microstructure but various surface oxides due to various surface finishing treatments is currently in progress.
Fatigue of oxidized superelastic NiTi wires was investigated by cyclic tensile tests in simulated biofluid. Although the static NiTi wire is highly corrosion resistant thanks to the thin passive TiO2 oxide layer covering its surface, the same NiTi wire, when strained cyclically in the liquid, suffers from environmentally induced fatigue degradation and preliminary failure. As the thin TiO2 surface oxide cannot withstand the large superelastic strains, the wire is in fact covered by a “cracked surface oxide” containing dense array of regularly spaced microcracks that open/close periodically upon cycling and expose fresh NiTi surface to the liquid. Fatigue lifetime of superelastically NiTi wire is shorter in the liquid compared to the air.
The state of the surface of the cyclically deformed NiTi wire was continuously monitored by following the evolution of the electrochemical Open Circuit Potential alongside with the macroscopic stress and strain. The OCP signal reflects mechanically induced local breakdown of the passive oxide layers triggering the chemical reactions on the wire surface. Microcracks on the surface of the stretched fatigued wire as well as on the FIBed cross section were observed by SEM. Based on the results, it is claimed that fatigue lifetime of superelastic NiTi wire deforming cyclically in simulated biofluid is controlled by mechanically driven chemical reactions (passivation) at the excessively stretched surface leading to hydrogen generation at the tips of the periodically opening/closing cracks (freshly opened bare NiTi/liquid interface).
Mechanism of environmental fatigue degradation of NiTi is proposed consisting in the adsorption of the generated hydrogen by the mechanically loaded surface, diffusional transfer of the adsorbed hydrogen into the bulk facilitated by the interfaces moving during the cyclic martensitic transformation, and local suppression of the martensitic transformation in hydrogen-affected areas. This mechanism assists crack nucleation under the surface oxide cracks and facilitates growth of selected cracks into the matrix, which ultimately leads to the brittle fracture of the NiTi wire. Major cracks always nucleate at inclusions or notches on the surface.
The mechanism explains the origin of clinical observations of random embrittlement and fractures of NiTi wires taken from explanted tracheal and esophageal NiTi stents.
Support from the research Projects GAČR 14-36566G (J. Racek), P107/12/0800 (L. Heller), and GA14-15264S (P. Šittner) of the Grant Agency of the Czech Republic and project FUNBIO - CZ.2.16/3.1.00/21568 is acknowledged. The authors thank Ing. J. Pilch and Ing. L. Kaderavek for their assistance with the design and fabrication of the in situ electrochemical loading rig and Ing. K. Hiřmanová, who carried out the long-time immersion tests. The authors thank the company TESCAN ORSAY HOLDING for assistance with special SEM experiments.
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