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At least 253 records · Page 14

Features of Crystallization of Rapidly Quenched Ni{sub 45}Ti{sub 32}Hf{sub 18}Cu{sub 5} and Ni{sub 25}Ti{sub 32}Hf{sub 18}Cu{sub 25} Alloys from Melt with High-Temperature Shape Memory Effect

A comparative study of the structure and the chemical and phase composition of Ni{sub 45}Ti{sub 32}Hf{sub 18}Cu{sub 5} and Ni{sub 25}Ti{sub 32}Hf{sub 18}Cu{sub 25} amorphous alloys obtained by fast-quenching of melt stream by spinning has been carried out by transmission and scanning electron microscopy and X-ray diffraction. The critical temperatures of their devitrification were determined by the data of temperatures measurements of electrical resistance. The features of the formation of ultrafine structure and the phase transformation at the vitrification depending on the regimes of heat treatment and chemical composition of alloy have been established.

75 CONDENSED MATTER PHYSICS, SUPERCONDUCTIVITY AND↗

Magnetic structure and phase transition of Ni 2 Mn 1.48 Sb 0.52 magnetic shape memory compound

Here, a comprehensive study of the structural and magnetic properties of the Ni 2 Mn 1.48 Sb 0.52 compound is presente using neutron diffraction and magnetic measurements. It is found that Mn atoms on 4a and 4 sites are ferrimagnetic coupled in the austenitic phase. At 300 K, the magnetic moments of Mn (4a) an Mn (4b) are determined to be 2.72(3) μ B and -2.67(5) μ B , respectively. From 260 K to 4 K, the compound is in martensite phase and the magnetic moments of Mn (2a), Mn (2f), Mn (2b), Mn (2e) at 4 K ar 2.2(5) μ B , 2.3(5) μ B , -2.1(5) μ B , and -2.6(5) μ B , respectively.

36 MATERIALS SCIENCE↗

Influence of Cobalt and Molybdenum Additives on the Structure and Shape Memory Parameters of Reaction-Sintered Porous Nickel Titanium Alloys

We have studied the structure and properties of porous nickel titanium (TiNi) alloys obtained upon reaction sintering of Ti and Ni powders with Co and Mo additives. It is established that Co and Mo doping additives retain the compaction of Ni powder achieved at the initial stage of sintering. The maximum deformation of porous samples loaded in the austenite state was observed upon adding Co, while the addition of Mo resulted in minimum deformation. The addition of Co leads to single-stage martensitic transformation in TiNi phase, while the addition of Mo leads to the two-stage transformation that is more homogeneous over the volume. Both Co and Mo additives lead to increase in the maximum accumulated strain due to the formation of favorably oriented stress-induced martensite and reoriented quench-induced martensite.

75 CONDENSED MATTER PHYSICS, SUPERCONDUCTIVITY AND↗

Formation of microcraters and hierarchically-organized surface structures in TiNi shape memory alloy irradiated with a low-energy, high-current electron beam

The regularities of surface cratering in TiNi alloy irradiated with a low-energy, high-current electron beam (LEHCEB) in dependence on energy density and number of pulses are studied. LEHCEB processing of TiNi samples was carried out using RITM-SP facility. Energy density E{sub s} was varied from 1 to 5 J/cm{sup 2}, pulse duration was 2.5–3.0 μs, the number of pulses n = 1–128. The dominant role of non-metallic inclusions [mainly, TiC(O)] in the nucleation of microcraters was found. It was revealed that at small number of pulses (n = 2), an increase in energy density leads both to increasing average diameter and density of microcraters. An increase in the number of pulses leads to a monotonic decrease in density of microcraters, and, therefore, that of the proportion of the area occupied by microcraters, as well as a decrease in the surface roughness. The multiple LEHCEB melting of TiNi alloy in crater-free modes enables to form quasi-periodical, hierarchically-organized microsized surface structures.

36 MATERIALS SCIENCE↗

Effects of Heat Input on Weld-Bead Geometry, Surface Chemical Composition, Corrosion Behavior and Thermal Properties of Fiber Laser-Welded Nitinol Shape Memory Alloy

Bead-on-plate laser welding was carried out on 1-mm-thick Nitinol sheets at different heat input values. The variations in weld-bead geometry and variations in microstructures across the bead were studied. The effects of heat input on surface layer composition of the welded samples, corrosion properties and phase transformation temperature were examined. From x-ray photoelectron spectroscopy (XPS), it was clear that relative intensity of elemental Ni peak was higher in parent material and the oxidation state of Ti was Ti{sup 4+}. It was further observed from Auger electron spectroscopy (AES) that the Ti to Ni ratio on the top surface of the welded samples was more than 1, and as a result of this the stability of TiO{sub 2} layer was enhanced, which eventually helped to improve the corrosion property of the welded samples. The polarization resistance of the welded samples was increased by more than ten times compared to that of the un-welded samples. From differential scanning calorimetry (DSC), it became evident that phase transformation temperatures got changed due to welding.

36 MATERIALS SCIENCE↗

Stacking faults and alternate crystal structures for the shape-memory alloy NiTi

Here, we use ab initio calculations to study the role of stacking faults in connecting the high-temperature B2 and the theoretically predicted low-temperature B33 NiTi phases. In contrast with prior work, we describe the B 2 → B 33 phase transformation in terms of alternate bilayer shifts by 1 2 [100] on the ( 011 ) B 2 plane, obtaining a viable pathway; the same mechanism could also work with the B19 parent phase. We then examine B33-like structures built from alternate stacking sequences of B19 bilayers, constructed to have monoclinic tilt angles close to the experimentally reported NiTi B19' martensite, and find four low-energy stacking-fault variants with energies 5.8–8.5 meV/atom above the calculated B19' martensite structure, suggesting that such structures might appear as a part of the NiTi martensite phase at low temperatures. Investigating further the occurrence of specific coordinated planar shifts in NiTi systems, we report a dynamically stable NiTi B27 phase and find that it is only 1.2 meV/atom above the calculated B33 ground-state structure, thus having a potential to also play a role in NiTi martensitic phase transformation.

36 MATERIALS SCIENCE↗

Protective Properties of Aluminum Nitride Coatings by DC-PVD Sputtering on Cu-10Al-13Mn Shape Memory Alloy

The AlN coating was applied on the surface of a Cu-10Al-13Mn alloy using the DC-PVD sputtering method. The substrate was set at three different temperatures which were ambient, 100 and 200 °C. The effect of the substrate temperature on the quality of AlN coating was modeled by simulating stress on the coating and substrate. The preparation, microstructure, and corrosion resistance of the coating were studied. The surface morphology and element distribution of the coating were investigated by scanning electron microscopy (SEM) and energy distribution spectroscopy (EDS), respectively. In addition, the corrosion resistance of coating was measured using electrochemical impedance spectroscopy (EIS) method in 1 M NaCl solution. The results showed that the AlN coating was formed on the Cu-10Al-13Mn alloy by DC-PVD sputtering method and the AlN coating considerably improved the corrosion resistance of Cu-10Al-13Mn alloy in the given corrosive media. According to EIS test, polarization resistance increased from approximately 1.6 to 115 KΩ, at 200 °C for uncoated and coated samples, respectively. Thus, corrosion resistance of AlN coating improved with the increase in the substrate temperature during the DC-PVD sputtering process.

36 MATERIALS SCIENCE↗

On the fast kinetics of B2–L2 1 ordering in Ni-Co-Mn-In metamagnetic shape memory alloys

B2–L2 1 configurational order resulting from thermal processing of Ni-Co-Mn-In Heusler alloys is one of the main factors defining the characteristics of the martensitic transformation experienced by these alloys. While the effects of the quenched-in disorder on the martensitic transformation have been extensively investigated, the kinetics of the ordering process is not well known and mostly inferred from the indirect results such as the dependence of the martensitic transformation or magnetic transition temperatures to thermal processing. However, recent results suggested that the kinetics of B2– L 2 1 ordering could have a more significant role than expected in the final state of the material and its functional properties. In the current work, an attempt has been made to investigate the kinetics of B2–L2 1 ordering in order to evaluate the dependence of the quenched-in disorder on the different variables of the thermal procedures. Results showed that ordering rate has a strong dependence on annealing temperature. Below 600 K, slow kinetics is forcing the crystal to always contain a certain amount of quenched-in disorder at room temperature. Between 600 K and 750 K, kinetics is fast enough to reach thermal equilibrium state within tens of minutes during the annealing process. Above 750 K, kinetics is very fast and thermal equilibrium can be reached during heating, so no isothermal holding is required. Furthermore, these predictions have been confirmed using differential scanning calorimetry and in-situ high-energy X-Ray diffraction measurements for non-direct estimations of the degree of order.

36 MATERIALS SCIENCE↗

Shape memory in self-adapting colloidal crystals

We report reconfigurable, mechanically responsive crystalline materials are central components in many sensing, soft robotic, and energy conversion and storage devices1,2,3,4. Crystalline materials can readily deform under various stimuli and the extent of recoverable deformation is highly dependent upon bond type1,2,5,6,7,8,9,10. Indeed, for structures held together via simple electrostatic interactions, minimal deformations are tolerated. By contrast, structures held together by molecular bonds can, in principle, sustain much larger deformations and more easily recover their original configurations. In this report we study the deformation properties of well-faceted colloidal crystals engineered with DNA. These crystals are large in size (greater than 100 µm) and have a body-centred cubic (bcc) structure with a high viscoelastic volume fraction (of more than 97%). Therefore, they can be compressed into irregular shapes with wrinkles and creases, and, notably, these deformed crystals, upon rehydration, assume their initial well-formed crystalline morphology and internal nanoscale order within seconds. For most crystals, such compression and deformation would lead to permanent, irreversible damage. The substantial structural changes to the colloidal crystals are accompanied by notable and reversible optical property changes. For example, whereas the original and structurally recovered crystals exhibit near-perfect (over 98%) broadband absorption in the ultraviolet–visible region, the deformed crystals exhibit significantly increased reflection (up to 50% of incident light at certain wavelengths), mainly because of increases in their refractive index and inhomogeneity.

36 MATERIALS SCIENCE↗

Shape memory polymer blend materials

An object comprising: a blend of (i) a phenol-containing polymer and (ii) a nitrile butadiene rubber; wherein the phenol-containing polymer is present in an amount of at least 5 wt % and up to about 95 wt % by total weight of components (i) and (ii). The object may further contain an electrically conducting component dispersed within the blend or on a surface of the blend. Also described is a method of thermal-activated reversible mechanical deformation of the object by (i) deforming the object at a first temperature, which is at or above the glass transition temperature of the object, and applying a stress on the object; (ii) fixing the deformed state by cooling the object to a second temperature of no more than 0° C. while under stress, and removing the stress; and (iii) recovering the object to the original shape by raising the temperature of the object to the first temperature.

Naskar, Amit K.↗

Harvesting Mechanical and Thermal Energy by Combining ZnO Nanowires and NiTi Shape Memory Alloy

In the expanding world of small scale energy harvesting, the ability to combine thermal and mechanical harvesting is growing ever more important. Here, we demonstrate the feasibility of using ZnO nanowires to harvest both mechanical and low-quality thermal energy in simple, scalable devices. These devices were fabricated on kapton films and used ZnO nanowires with the same growth direction to assure alignment of the piezoelectric potentials of all of the wires. Mechanical harvesting from these devices was demonstrated using a periodic application of force, modeling the motion of the human body. Tapping the device from the top of the device with a wood stick, for example yielded an Open Circuit Voltage (OCV) of 0.2 - 4 V, which is in an ideal range for device applications. In order to demonstrate thermal harvesting from low quality heat sources, a commercially available Nitinol (Ni-Ti alloy) foil was attached to the nanowire piezoelectric device to create a compound thermoelectric. When bent at room temperature and then heated to 50°C, the Nitinol foil was restored to its original flat shape, which yielded an output voltage of nearly 1 V from the ZnO nanowire device.

36 MATERIALS SCIENCE↗