Characterization and corrosion behavior of NiTi–Ti2Ni–Ni3Ti multiphase intermetallics produced by vacuum sintering

An in-situ synthesis method was employed to produce NiTi–Ti₂Ni–Ni₃Ti multiphase intermetallics. In this regard, the amorphous/nanocrystalline Ni–Ti powders were sintered at 1300 °C for 2 hrs to obtain Ni–Ti alloys with dense structure. Tafel polarization tests were employed to study corrosion behavior of multiphase materials in 3.5% NaCl and 0.1 M H₂SO₄ corrosive media. The results indicated that the microstructure of sintered samples consists of NiTi(Fe) and Ti₂Ni/Ti₄Ni₂O_x phases embedded in a Ni₃Ti matrix. The synthesized multiphase materials had microhardness up to 873 HV1 kg.Further investigations showed the corrosion performance of multiphase samples in 3.5% NaCl solution was inferior to that of wrought NiTi alloy. In contrast, the corrosion resistance of multiphase samples in 0.1 M H₂SO₄ solution was comparable to that of wrought NiTi alloy.     

Corrosion behavior of Zr41.2Ti13.8Ni10Cu12.5Be22.5 bulk metallic glass in various aqueous solutions

In this study electrochemical corrosion behavior of Zr_41.2Ti_13.8Ni₁₀Cu_12.5Be_22.5 bulk metallic glass (BMG) in various aqueous solutions (3.5% NaCl, 1 N HNO₃, H₂SO₄ and HCl) in order to compare with 316L stainless steel were thoroughly investigated. Scanning electron microscopy (SEM) was used to evaluate the influence of corrosion on the surface topography in immersion specimens to examine where the corrosion pits initiated. Corrosion rate of Zr_41.2Ti_13.8Ni₁₀Cu_12.5Be_22.5 BMG in 3.5% NaCl solution was ∼0.6 mpy and its excellent corrosion resistance can be concluded. Polarization and SEM results also vouched a remarkable corrosion resistance of Zr_41.2Ti_13.8Ni₁₀Cu_12.5Be_22.5 BMG in 3.5% NaCl aqueous solution in comparison with 316L stainless steel.     

Determination of corrosion rate of orthodontic wires based on nickel‐titanium alloy in artificial saliva

The goal of this study was to determine corrosion behavior of three orthodontic wires based on nickel‐titanium alloy (NiTi) in artificial saliva at temperature of 37 °C as function of immersion time. Following orthodontic wires were used: uncoated (NiTi), rhodium coated (Rh NiTi) and nitrified (N NiTi) orthodontic wires. Corrosion of investigated orthodontic wires were monitored by measuring of Ni²⁺ and Ti⁴⁺ ions released in artificial saliva by inductively coupled plasma‐optical emission spectroscopy (ICP‐OES) after 3, 7, 14, 21 and 28 days of immersion. Obtained results indicate that corrosion reaction of the NiTi wires in artificial saliva follows the parabolic rate law. According to the obtained values of parabolic corrosion rate constants, corrosion susceptibility of orthodontic wires decreases in the following order: Rh NiTi wire (K_p = 2.48 μg²/cm⁴ h) > NiTi wire (K_p = 1.6 × 10^–3 μg²/cm⁴ h) > N NiTi wire (K_p = 6.0 × 10^–4 μg²/cm⁴ h). These results indicate that in comparison with uncoated NiTi wire, rhodium coating significantly increases corrosion susceptibility, while nitrification effectively suppresses the release of Ni²⁺ and Ti⁴⁺ ions.     

Formation of reactive layers in brazed Ti and Cu using a melt-spun Zr41.2Ti13.8Ni10.0Cu12.5Be22.5 alloy

Investigations on the microstructure of brazed Ti and Cu when using a Zr_41.2Ti_13.8Ni_10.0Cu_12.5Be_22.5 alloy revealed that mainly Ti-rich compounds were formed at the brazed joint after brazing at 790 °C for 10 min. However, detailed microstructural investigations revealed that the interfacial areas close to the Cu consisted of orthorhombic Cu₄Ti, orthorhombic Cu₃Ti, hexagonal Cu₂TiZr and tetragonal CuTi compounds. The formation of a Cu₂TiZr Laves phase at the interfacial areas close to the Cu possibly suppresses a diffusion of Cu into the central areas of the brazed joint due to its characteristics of a high solubility and high melting temperature.     

Corrosion behaviour of amorphous Ti48Cu52, Ti50Cu50 and Ti60Ni40 alloys investigated by potentiodynamic polarization method

Potentiodynamic polarization studies were carried out on virgin specimens of amorphous alloys Ti₄₈Cu₅₂, Ti₅₀Cu₅₀ and Ti₆₀Ni₄₀ in 0.5 M HNO₃, 0.5 M H₂SO₄ and 0.5 M NaOH aqueous media at room temperature. The value of the corrosion current density (I_corr) was maximum for Ti₄₈Cu₅₂ alloy in all the three aqueous media as compared to the remaining two alloys. The value of I_corr for the alloy Ti₄₈Cu₅₂ was maximum (I_corr = 2.6 × 10^{- 5} A/cm²) in 0.5 M H₂SO₄ and minimum (I_corr = 3.5 × 10^{- 6} A/cm²) in 0.5 M NaOH aqueous solutions. In contrast, the alloy Ti₆₀Ni₄₀ exhibited the least corrosion current density in 0.5 M HNO₃ (I_corr = 40 × 10^{- 7}A/cm²) and in 0.5 M NaOH (I_corr = 5.5 × 10^{- 7} A/cm²) aqueous media as compared to those for Ti-Cu alloys, while its value in 0.5 M H₂SO₄ was comparable to that for Ti₄₀Cu₅₀. It is suggested that the alloy Ti₆₀Ni₄₀ is more corrosion resistant than the alloys Ti₄₈Cu₅₂ and Ti₅₀Cu₅₀ in all the three aqueous media.     

Influence of heat treatment on the fatigue life of a laser-welded NiTi alloy wire

The influence of heat treatment on the rotating–bending fatigue of a laser-welded superelastic NiTi alloy wire was investigated. In comparison with the as-welded and annealed at 500 °C for 1 h specimens, the specimen annealed at 400 °C for 1 h shows the best fatigue resistance. The difference of fatigue life in the heat-treated materials is attributed to the different Ti₃Ni₄ precipitate size. Heat treatment to produce smaller coherent precipitates (10 nm) improves the fatigue resistance of the laser-welded NiTi alloy wire. When the Ti₃Ni₄ precipitates become coarse, the fatigue resistance decreases.     

The electrochemical behavior of a Ti50Ni47Fe3 shape memory alloy

The corrosion performance of Ti₅₀Ni₄₇Fe₃ alloy in 0.9% NaCl physiological, artificial saliva and Hank's solutions with different pH values at 37 °C was investigated by means of open circuit potential (OCP) measurement and linear polarization (LP) measurement techniques, respectively. The OCP stabilized at − 0.2925, − 0.3111 and − 0.3454 mV/SCE in sequence for 0.9% NaCl, artificial saliva and Hank's solutions, respectively. LP results demonstrated that the Ti₅₀Ni₄₇Fe₃ alloy has a low passive current and a wide passive range. The surface roughness and in-depth distribution of the passive films after immersion in corrosion media was characterized by using Atomic Force Measurement (AFM) and X-ray electron spectroscopy (XPS). AFM results shows that the electrochemical measurements have little influence on the surface roughness of the Ti₅₀Ni₄₇Fe₃ alloy, and the XPS analysis results revealed that the outer passive film consisting mainly of a layer of TiO₂ which is deemed to be important for all biomaterials.     

Effects of anodic oxidation in H2SO4 electrolyte on the biocompatibility of NiTi shape memory alloy

Effects of anodic oxidation in H₂SO₄ electrolyte on the biocompatibility of NiTi shape memory alloy (SMA) were investigated by characterizing surface structure, blood compatibility, wettability, release of harmful Ni ions of anodized NiTi SMA. Although titania film resulting from anodic oxidation in H₂SO₄ electrolyte has a porous structure, it can effectively block out-diffusion of Ni from NiTi SMA to simulated body fluid (SBF). Comparing with chemical polishing, anodic oxidation in H₂SO₄ electrolyte can also improve the wettability, blood compatibility, thromboresistance of NiTi SMA.     

Multiple-step martensitic transformations in the Ni51Ti49 single crystal

Multiple-step martensitic transformations of an aged Ni₅₁Ti₄₉ single crystal using calorimetric method were investigated. Results show that for short aging times (10–45 min) multiple-step martensitic transformations on cooling occur in two steps. Applying intermediate aging times (1.25–4 h) results in three steps and long aging times (more than 8 h) lead to two-step martensitic transformations again. This behavior has not been recognized in NiTi single crystals in literatures. It can be related to the heterogeneity of composition and stress fields around Ni₄Ti₃ precipitates.     

Effect of aging on martensitic transformation behavior of Ti48.8Ni50.8V0.4 alloy

In this article, the effect of aging on martensitic transformation of Ti_48.8Ni_50.8V_0.4 alloy was investigated. The results show that the martensitic transformation of the solution-treated shape memory alloy is a typical single-stage transformation process. The transformation temperatures of the samples aged at different temperatures for 0.5 h were lower as compared to that of the solution-treated alloy. With the increase of aging temperature, the transformation temperatures increase. After aging at 500 °C, the samples exhibit a multiple-stage transformation. The samples after aging at 500 °C for more than 5 h resulted in the transformation sequence of A → R→M1 and A → M2 upon cooling and M2 → A and M1 → A upon heating.     

Phase formation in Ti/Ni dissimilar welds

We explore phase formation in Ti/Ni dissimilar welds using a combination of microscopy and composition analysis (TEM, SEM and EDS). Main microstructural features are NiTi dendrites and Ti₂Ni grains in the inter-dendritic space. The high temperature B2 phase of NiTi is found to transform to trigonal ‘R’-phase, B19^′martensite, and rhombohedral Ni₄Ti₃ phase; these different transformation products highlight the composition inhomogeneity in the parent B2 phase and probable non-equilibrium solidification events during rapid cooling of the weld. Solidification sequence of NiTi and Ti₂Ni was found to vary depending on local conditions in the weld. Formation of impurity nitride phases of titanium is observed which signify incomplete shielding during welding.     

Preparation of NixTiy compound via Ni plating followed by thermal treatment of Ti powder

In this research, Ni_xTi_y compound was prepared by thermal treatment of Ni-plated Ti powder. For this purpose, Ti powder was plated in an electroless Ni bath for various times (120, 225, 300, and 720?min). Hydrazine hydrate was used as a reductant for the deposition of pure Ni on the Ti particles. The plated powder (225?min) was heat treated under argon atmosphere to achieve Ni_xTi_y powder. Finally, the heated/plated powder was pressed by CIP followed by sintering at 980°C for prepare the Ni_xTi_y bulk sample. The plated powders as well as sintered one were characterized using scanning electron microscopy, energy dispersive spectrometer, X-ray fluorescence, X-ray diffraction and differential scanning calorimetric. The NiTi₂, NiTi, and Ni₃Ti phases were detected in the XRD patterns of heated/plated Ti powder. According to DSC data, the heated/plated Ti powder showed reversible martensitic transformation at temperature range of ?38.0°C to +38.1°C, while sintered/heated/plated Ti powder displayed reversible transformation at temperature range of 16.0°C–15.4°C.     

Fabrication and characterization of NiTi shape memory alloy synthesized by Ni electroless plating of titanium powder

In this work NiTi shape memory alloy was fabricated from mixed elemental powders, Ni plated titanium powder and Ni heated/plated titanium powder by Ar-sintering. Electroless plating process was utilized to fabricate Ni plated titanium powder. For this purpose titanium powder was plated in an electroless Ni bath for 225?min and hydrazine hydrate was used as a reductant to deposit pure nickel on the titanium particles. Ni plated titanium powder was heat treated under an argon atmosphere at 1000?°C to prepare Ni heated/plated titanium powder. Finally, the three sample powders were pressed by CIP followed by sintering at 980?°C for 8?h to manufacture NiTi shape memory alloy. The prepared powders, as well as sintered samples, were characterized by scanning electronic microscopy (SEM), energy dispersive spectrometer analysis (EDS), X-ray fluorescence (XRF), X-ray diffraction (XRD) and differential scanning calorimetric (DSC). The results indicated the presence of NiTi phase and also non-transformable phases (NiTi₂ and Ni₃Ti) in the heated/plated Ti powder and sintered samples. NiTi compound was dominated phase in the heated/plated sintered sample. All three sintered samples, as well as heated/plated powder, showed one-step phase transformation (B2???B19′).     

Crystallization kinetics and martensitic transformation of Ti49Ni46.5Ce4.5 alloy thin film

The Ti₄₉Ni_46.5Ce_4.5 alloy thin film was prepared by direct current (DC) magnetron sputtering system for the first time. Crystallization kinetics, phase composition and the behaviors of martensitic transformation were studied. The results by X-ray diffraction (XRD) and differential scanning calorimeter (DSC) demonstrated that the primary second phase of TiNiCe alloy thin films was Ce₂Ni₇ phase, apparent activation energy was determined to be 510 kJ/mol at the continuous heating process, Avrami exponents for different isothermal temperature were in the range of 1.1-1.88 between 713 and 730 K, one-step martensitic transformation was observed in the crystallized Ti₄₉Ni_46.5Ce_4.5 alloy thin films. The influence of thermal process on martensitic transformation temperature was investigated with non-isothermal and isothermal crystallization. The reason behind the transformation temperature change was also discussed.     

Effects of plate thickness on reverse martensitic transformation of prestrained NiTi/NiTi alloy

In this paper, differential scanning calorimeter (DSC) was used to study the effects of predeformation and plate thickness on the reverse martensitic transformation of explosively welded NiTi/NiTi alloy. Results showed that there was a constraint between Ni_50.4Ti (NiTi-1) and Ni_49.8Ti (NiTi-2), which led to that the thickness of NiTi-1 or NiTi-2 strongly affected the reverse martensitic transformation behavior because residual stress variations in thickness wound enable bias force to be built inside the composite. The DSC measurements showed that after deformation, the reverse martensitic transformation temperature of the composite was increased with the increasing thickness of NiTi-2. Also, the XRD results revealed that the microstructure of NiTi/NiTi alloy changed from B2 phase to B19’ phase along the thickness direction.     

Microstructure and martensitic transformation and mechanical properties of cast Ni rich NiTiCo shape memory alloys

Abstract

The influence of Co additions on the microstructure, second phase precipitates, phase transformation and mechanical properties of cast Ni_51?xTi₄₉Co_x (x?=?0, 0·5, 1·5 and 4 at-%) shape memory alloys was investigated. At the expense of Ni, Co added to NiTi alloy significantly increases the martensitic transformation temperature. The matrix phase in the microstructure of Ni₅₁Ti₄₉Co₀ alloy is the austenite phase (B2) in addition to martensite phase (B19′) and precipitates of NiTi intermetallic compounds. However, the parent phase in the other three alloys, Ni_50·5Ti₄₉Co_0·5, Ni_49·5Ti₄₉Co_1·5 and Ni₄₇Ti₄₉Co₄, is martensite. Ti₂Ni phase was found in the microstructures of the all investigated alloys; however, Ni₃Ti₂ phase precipitated only in the NiTi alloy with 0 at-%Co. The volume fraction of Ti₂Ni phase decreased by the additions of 0·5 and 1·5 at-%Co, while it is slightly increased with 4 at-%Co. The hardness value of NiTi alloy is affected by Co additions.     

A study on the hot corrosion behavior of Ti-6Al-4V alloy

The titanium alloys are potential materials for high temperature applications in turbine components due to their very high temperature strength and lightweight properties. However, hot corrosion is a life-limiting factor when Ti alloys are exposed to different chemical environments at high temperature. In the present paper, hot corrosion behavior of Ti-6Al-4V (Ti-31) alloy in different salt environments viz. air, Na₂SO₄-60% V₂O₅ and Na₂SO₄-50% NaCl at 750 °C was studied. The parabolic rate constants were calculated for different environments from the thermo-gravimetric data obtained for the samples and they show that corrosion rate is minimum in air when compared to chemical environment. The scale formed on the samples upon hot corrosion was characterized by using X-ray diffraction (XRD), SEM, and EDAX analysis to understand the degradation mechanisms.     

Effect of Ba deoxidation on oxygen content in NiTi alloys and non-metallic inclusions

The effect of Ba deoxidation on the oxygen content and non-metallic inclusions in NiTi alloys was investigated. The NiTi alloy melt was held in a CaO crucible at 1673 K under Ar gas flow for 0–600 s. Metallic Ba (0.5–1.5 mass% with respect to NiTi alloy melt) was added to the melt. After melting, oxygen content of 710 and 330 mass ppm decreased to 210 and 130 mass ppm, respectively, after a holding time of 300 s after the addition of Ba. The oxygen in the melts was reduced to as low as 64 mass ppm after a second Ba deoxidation. The non-metallic inclusions observed in the NiTi alloys were the Ti₄Ni₂O _X and Ti(C,N,O) _X types. Decreased oxygen content through Ba deoxidation caused a change in the main phase of the non-metallic inclusions from the Ti₄Ni₂O _X type to the Ti(C,N,O) _X type, and a decrease in the area percents of the non-metallic inclusions.     

Microstructure development during dissimilar welding: Case of laser welding of Ti with Ni involving intermetallic phase formation

Development of solidification microstructure in a laser welded Ti/Ni dissimilar binary couple is presented. At the fusion interfaces in both Ti and Ni, growth of the base metal grains into the weld pool is inhibited by the presence of composition gradients in the melt. Ti₂Ni dendrites grow toward the base metal at the Ti fusion interface. In the Ni side, appearance of a nickel solid solution phase is followed by layers of Ni₃Ti, Ni₃Ti+NiTi eutectic, and NiTi. NiTi dendrites and Ti₂Ni constitute the microstructure in the middle of the weld. Isolated titanium dendrites are observed throughout the weld, but their preferential occurrence toward the top surface of the weld is more prominent. Results are rationalised on the basis of interplay of the transport processes in the weld with the thermodynamics of the Ti-Ni system.     

Microstructure and martensitic transformation of Ti49Ni51 − xHfx high temperature shape memory alloys

In present work, the microstructure and martensitic transformation of Ti₄₉Ni_51 − xHf_x (x = 3-15) alloys were studied. The microstructure of Ti₄₉Ni_51 − xHf_x alloys consists of B19′ martensite and (Ti,Hf)₂Ni phase at room temperature. The martensitic transformation behavior is characterized by a single-stage transformation. With increasing Hf content, the transformation temperature increases from 75 to 279 °C resulting from the reduced valence electron concentration, indicating that the replacement of Hf for Ni is effective in increasing the transformation temperatures. The results suggest that the Ti₄₉Ni_51 − xHf_x shape memory alloy is one of potential candidates for high temperature applications.