Characterization of NiTi Shape Memory Wires by Differential Scanning Calorimetry and Transmission X-ray Diffraction

1991 ◽  
Vol 246 ◽  
Author(s):  
Ming-Yuan Kao ◽  
Sepehr Fariabi ◽  
Paul E. Thoma ◽  
Husnu Ozkan ◽  
Louis Cartz
Keyword(s):  
Heat Treatment ◽  
Differential Scanning Calorimetry ◽  
Heat Treatment Temperature ◽  
Room Temperature ◽  
Cold Work ◽  
Treatment Temperature ◽  
X Ray Diffraction ◽  
Scanning Calorimetry ◽  
X Ray ◽  
Niti Wires

AbstractThe reversible transformations between the Austenite (A) and Martensite (M) phases of NITI shape memory wires having a 78°C austenlte finish temperature (950°C annealed) were studied In the cold work and heat treatment ranges between 14 to 62% and 400 to 525°C respectively. The ranges of peak Transformation Temperatures (TI), determined by Differential Scanning Calorimetry (DSC) at a 10°C/min rate, were found to be 56 to 75°C, -28 to 33°C, and 38 to 52°C for the respective high temperature A, low temperature M, and the Intermediate Rhombohedral (R) phases. The degree of cold work and heat treatment had significant effects on the TT of NITI wires. The peak TT of A and M decreases with Increasing cold work. Except for the 14% cold worked wires, the peak TT Increases with Increasing heat treatment temperature for M, and Increases with Increasing heat treatment temperature for A for temperatures higher than 450°C. The peak IT of R Increases with Increasing cold work and decreasing heat treat temperature.Using MoKα radiation, transmission x-ray diffraction analysis was utilized to determine the phases at room temperature on wires thinned down to 0.05 to 0.01 mm in diameter. The diffraction patterns of body-centered cubic austenite (132) and monodlinic martenslte (B19) for NITi were both Identified. In addition, extra diffraction lines observed for various samples were tentatively assigned to M and the Intermediate R-phase. Depending on the thermal history and the processing conditions, the NITI wires consist of either a pure M, a mixture of A and R, or a mixture of A, R, and M at room temperature.

Influence of Gd Addition on the Structure and Capability of Ni-Mn-In Metamagnetic Shape Memory Alloys

2012 ◽  
Vol 535-537 ◽  
pp. 950-953
Author(s):  
Li Na Bai ◽  
Gui Xing Zheng ◽  
Zhi Jian Duan ◽  
Jian Jun Zhang
Keyword(s):  
Differential Scanning Calorimetry ◽  
Magnetic Properties ◽  
Magnetic Property ◽  
Transition Temperature ◽  
Martensitic Transformation ◽  
Room Temperature ◽  
Vibrating Sample Magnetometry ◽  
X Ray Diffraction ◽  
Scanning Calorimetry ◽  
X Ray

The influences of Gd concentration on martensitic transformation and magnetic properties of NiMnIn alloys were investigated by differential scanning calorimetry (DSC) , vibrating sample magnetometry (VSM), X-ray diffraction (XRD) and etc. It is Observed through the experiment: the addition of Gd enhances martensite transition temperature;X-ray diffraction analysis of experimental alloys is revealed that to the mixture is martensite and austenite at room temperature; content of Gd is not proportional to the improvement of magnetic property.

Study of thermal properties of Ga0.5In1.5Se3 by differential scanning calorimetry

2021 ◽  
pp. 2150407
Author(s):  
S. I. Ibrahimova
Keyword(s):  
Crystal Structure ◽  
Differential Scanning Calorimetry ◽  
Thermal Properties ◽  
Thermal Effects ◽  
Room Temperature ◽  
Structural Studies ◽  
X Ray Diffraction ◽  
Hexagonal Symmetry ◽  
Scanning Calorimetry ◽  
X Ray

The crystal structure and thermal properties of the [Formula: see text] compound have been investigated. Structural studies were performed by X-ray diffraction at room temperature. The crystal structure of this compound was found to correspond to the hexagonal symmetry of the space group P61. Thermal properties were studied using a differential scanning calorimetry (DSC). It was found in the temperature range [Formula: see text] that thermal effects occur at temperatures [Formula: see text] and [Formula: see text]. The thermodynamic parameters of these effects are calculated.

Preparation and Catalytic Performance of Ti(SO4)2/γ-Al2O3 Catalysts for Oligomerization of 1-Butene

2013 ◽  
Vol 634-638 ◽  
pp. 696-700
Author(s):  
Lin Jiu Xiao ◽  
Peng Li ◽  
Yong Gang Sheng
Keyword(s):  
Heat Treatment ◽  
Physicochemical Properties ◽  
Heat Treatment Temperature ◽  
Catalytic Performance ◽  
Treatment Temperature ◽  
Impregnation Method ◽  
X Ray Diffraction ◽  
Isothermal Adsorption ◽  
X Ray ◽  
Adsorption Desorption

A series of Ti(SO4)2/γ-Al2O3 catalysts were prepared by impregnation method and the catalytic performance of these catalysts in 1-butene oligomerization was investigated. The heat treatment temperature played great influences on the catalytic performance of these catalysts in the oligomerization. 90.1 wt.% conversion of 1-butene and 92.2 wt.% selectivity of dimers were obtained on Ti(SO4)2/γ-Al2O3(450) catalyst at 80 °C, 1.0 Mpa and LHSV=0.6 h−1. The heat treatment temperature determined the crystallinity of TiOSO4 and specific surface area of these catalysts, which affected the catalytic performance of these catalysts in 1-butene oligomerization. In addition, the physicochemical properties of these catalysts were comparatively characterized by powder X-ray diffraction (XRD), N2 isothermal adsorption-desorption techniques.

scholarly journals Influence of Different Heat Treatment Temperatures on the Microstructure, Corrosion, and Mechanical Properties Behavior of Fe-Based Amorphous/Nanocrystalline Coatings

Coatings ◽  
2019 ◽  
Vol 9 (12) ◽  
pp. 858
Author(s):  
Shenglin Liu ◽  
Yongsheng Zhu ◽  
Xinyue Lai ◽  
Xueping Zheng ◽  
Runnan Jia ◽  
...  
Keyword(s):  
Heat Treatment ◽  
Corrosion Resistance ◽  
Heat Treatment Temperature ◽  
Annealing Treatment ◽  
Treatment Temperature ◽  
X Ray Diffraction ◽  
Crystalline Phases ◽  
X Ray ◽  
Different Temperatures ◽  
Sprayed Coating

Fe-based amorphous/nanocrystalline coatings with smooth, compact interior structure and low porosity were fabricated via supersonic plasma spraying (SPS). The coatings showed outstanding corrosion resistance in a 3.5% NaCl solution at room temperature. In order to analyze the effect of annealing treatment on the microstructure, corrosion resistance and microhardness, the as-sprayed coating was annealed for 1 h under different temperatures such as 350, 450, 550 and 650 °C, respectively. The results showed that the number of oxides and cracks in the coatings presented an obvious increase with increasing annealing temperature, and the corrosion resistance of the coatings showed an obvious reduction. However, the microhardness of coatings showed an important increase. The microhardness of the coating could reach 1018 HV when the heat treatment temperature reached 650 °C. The X-ray diffraction (XRD) results showed that there appeared a number of crystalline phases in the coating when the heat treatment temperature was at 650 °C. The crystalline phases led to the increase of the microhardness.

Synthesis of nanocomposite coating of electrodeposed amorphic layers of the Ni–P–W system

2020 ◽  
pp. 53-60
Author(s):  
A. V. Krasikov
Keyword(s):  
Electron Microscopy ◽  
Heat Treatment ◽  
Differential Scanning Calorimetry ◽  
Phase Composition ◽  
Diffraction Analysis ◽  
Nanocomposite Coating ◽  
Nanocrystalline Phase ◽  
X Ray Diffraction ◽  
Scanning Calorimetry ◽  
X Ray

The processes of the formation of the nanocomposite coating of Ni–11.5% P–5%W were studied during the heat treatment of amorphous electrodeposited layers. Using the method of differential scanning calorimetry, the temperature of the onset of crystallization of the nanocrystalline phase Ni3P was determined. X-ray diffraction analysis showed that heat treatment produces Ni3P phosphides and, presumably, Ni5P2, the size of which, according to electron microscopy, is 5–50 nm. The influence of the duration of heat treatment on the phase composition and microhardness of coatings is investigated.

Crystal Polymorphs and Multiple Crystallization Pathways of Highly Pressurized 1-Ethyl-3-Methylimidazolium Nitrate

2019 ◽  
Vol 72 (2) ◽  
pp. 87 ◽  
Author(s):  
Hiroshi Abe ◽  
Takahiro Takekiyo ◽  
Yukihiro Yoshimura ◽  
Nozomu Hamaya ◽  
Shinichiro Ozawa
Keyword(s):  
Differential Scanning Calorimetry ◽  
High Pressure ◽  
Room Temperature ◽  
Ambient Pressure ◽  
Optical Microscope ◽  
X Ray Diffraction ◽  
Scanning Calorimetry ◽  
X Ray ◽  
Low Temperature Crystallization ◽  
Temperature Crystallization

Crystal polymorphs and multiple crystallization pathways of a room-temperature ionic liquid (RTIL) were observed only under high pressure (HP). The RTIL was 1-ethyl-3-methylimidazolium nitrate, [C2mim][NO3]. The HP-crystal polymorphs were related to conformations of the C2mim+ cation, and the HP-crystal pathways determined by the presence or absence of the planar′ (P′) conformation of the C2mim+ cation were switched at the bifurcation pressure (PB). Above PB, modulated crystal structures derived from the HP-inherent P′ conformer. Simultaneous X-ray diffraction and differential scanning calorimetry measurements, accompanied by optical microscope observations, confirmed the normal low-temperature crystallization of [C2mim][NO3] under ambient pressure.

Adjusting Microstructure and Magnetic Properties of Ni-Mn-In Metamagnetic Shape Memory Alloys by Addition of Gd

2012 ◽  
Vol 535-537 ◽  
pp. 959-963
Author(s):  
Li Na Bai ◽  
Gui Xing Zheng ◽  
Jing Xin ◽  
Jian Jun Zhang
Keyword(s):  
Magnetic Field ◽  
Differential Scanning Calorimetry ◽  
Magnetic Properties ◽  
Shape Memory ◽  
Room Temperature ◽  
Vibrating Sample Magnetometry ◽  
X Ray Diffraction ◽  
Scanning Calorimetry ◽  
X Ray ◽  
Microstructure And Magnetic Properties

The influences of Gd concentration on martensitic transformation and magnetic properties of NiMnIn alloys were investigated by differential scanning calorimetry (DSC) , vibrating sample magnetometry (VSM), X-ray diffraction (XRD) and etc. It shows that addition of Gd enhances martensite transition temperature and that X-ray diffraction analysis of experimental alloys is revealed which the mixture is martensite and austenite at room temperature. These alloys show promise as a metamagnetic shape memory alloy with magnetic-field-induced shape memory effect.

Preparation and Characterization of β-Eucryptite Glass Ceramics

2012 ◽  
Vol 624 ◽  
pp. 134-137 ◽  
Author(s):  
Ping Zhai ◽  
Xiao Feng Duan ◽  
Da Qian Chen ◽  
Chong Hai Wang
Keyword(s):  
Heat Treatment ◽  
Expansion Coefficient ◽  
Heat Treatment Temperature ◽  
Glass Ceramics ◽  
Treatment Temperature ◽  
Structure And Properties ◽  
X Ray Diffraction ◽  
Solid Reaction ◽  
X Ray

In this paper, β-eucryptite glass ceramics were synthesized by using solid reaction method. Phase constitution, structure and properties of the material were studied by X-ray diffraction (XRD) and differential thermal analysis (DTA). Furthermore, the effects of heat treatment temperature and preservation time on the thermal expansion coefficient were also analyzed. The results showed that the crystallization temperature of β-eucryptite glass ceramics was in the range of 810-860 °C and the content was more than 90%. With the increase of heat treatment temperature, the material expansion coefficient decreased.

Synthesis of pure amorphous Fe2O3

1997 ◽  
Vol 12 (2) ◽  
pp. 402-406 ◽  
Author(s):  
X. Cao ◽  
R. Prozorov ◽  
Yu. Koltypin ◽  
G. Kataby ◽  
I. Felner ◽  
...  
Keyword(s):  
Differential Scanning Calorimetry ◽  
Particle Size ◽  
Room Temperature ◽  
Nitrogen Atmosphere ◽  
X Ray Diffraction ◽  
Scanning Calorimetry ◽  
X Ray ◽  
Air Atmosphere ◽  
Transmission Electron ◽  
Amorphous Nanoparticles

A method for the preparation of pure amorphous Fe2O3 powder with particle size of 25 nm is reported in this article. Pure amorphous Fe2O3 can be simply synthesized by the sonication of neat Fe(CO)5 or its solution in decalin under an air atmosphere. The Fe2O3 nanoparticles are converted to crystalline Fe3O4 nanoparticles when heated to 420 °C under vacuum or when heated to the same temperature under a nitrogen atmosphere. The crystalline Fe3O4 nanoparticles were characterized by x-ray diffraction and M¨ossbauer spectroscopy. The Fe2O3 amorphous nanoparticles were examined by Transmission Electron Micrography (TEM), Differential Scanning Calorimetry (DSC), Thermogravimetric Analysis (TGA), and Quantum Design SQUID magnetization measurements. The magnetization of pure amorphous Fe2O3 at room temperature is very low (<1.5 emu/g) and it crystallizes at 268 °C.

scholarly journals Crystal Structures and Thermal Properties of L-MnC4H4O6•2H2O and DL-MnC4H4O6•2H2O

2019 ◽  
Vol 12 (1) ◽  
pp. 78
Author(s):  
Takanori Fukami ◽  
Shuta Tahara ◽  
Arbi Dimyati
Keyword(s):  
Thermal Analysis ◽  
Differential Scanning Calorimetry ◽  
Room Temperature ◽  
Structural Parameters ◽  
Silica Gels ◽  
X Ray Diffraction ◽  
Scanning Calorimetry ◽  
X Ray ◽  
Weight Losses ◽  
Group Symmetries

Manganese L-tartrate dihydrate, L-MnC4H4O6&middot;2H2O, and manganese DL-tartrate dihydrate, DL-MnC4H4O6&middot;2H2O, crystals were grown at room temperature by the gel method using silica gels as the growth medium. Differential scanning calorimetry, thermogravimetric-differential thermal analysis, and X-ray diffraction measurements were performed on both crystals. The space group symmetries (monoclinic P21 and P2/c) and structural parameters of the crystals were determined at room temperature. Both structures consisted of slightly distorted MnO6 octahedra, C4H4O6 and H2O molecules, and O&ndash;H&middot;&middot;&middot;O hydrogen-bonding frameworks between adjacent molecules. Weight losses due to thermal decomposition of the crystals were found to occur in the temperature range of 300&ndash;1150 K. We inferred that the weight losses were caused by the evaporation of bound 2H2O molecules, and the evolutions of gases from C4H4O4 and of (1/2)O2 gas from MnO2, and that the residual black substance left in the vessels after decomposition was manganese oxide (MnO).

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