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.

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.

Influence of Magnetic Field on Magnetic Properties of Electrodeposited Co-Ni-P Nanowires

2014 ◽  
Vol 24 (3S1) ◽  
pp. 90-94 ◽  
Author(s):  
Le Tuan Tu ◽  
Luu Van Thiem ◽  
Pham Duc Thang
Keyword(s):  
Magnetic Field ◽  
Magnetic Properties ◽  
Room Temperature ◽  
Hysteresis Loops ◽  
Vibrating Sample Magnetometry ◽  
X Ray Diffraction ◽  
Xrd Pattern ◽  
X Ray ◽  
Structure And Morphology ◽  
The Magnetic Field

The magnetic properties in Co-Ni-P nanowires arrays with diameter of 200 nm were investigated. All the samples were prepared by electrodeposition method with pH of 5.5 and at room temperature. During the deposition, a magnetic field in range of 0 - 750 Oe was applied parallel to the wires axis. The crystalline structure and morphology of the samples were characterized by X-ray Diffraction (XRD) and Scanning Electron Microscopy (SEM), respectively. The hysteresis loops were measured at room temperature using vibrating sample magnetometry (VSM). The mixture of hcp phases of the Co-Ni-P based nanowires has been indicated by the XRD pattern. The obtained results show that with 750 Oe magnetic field applied during deposition we can obtain maximum coercivity value (2180 Oe). The \(M_{r}/M_{s}\) ratio was rapid increased when the magnetic field changed from 0 Oe to 750 Oe.

scholarly journals Nanocrystal, phase transformation and microstructure of Ni50Ti50 shape memory alloy

2018 ◽  
Vol 24 (02) ◽  
pp. 22-25
Author(s):  
Dovchinvanchig M ◽  
Chunwang Zhao
Keyword(s):  
Differential Scanning Calorimetry ◽  
Phase Transformation ◽  
Shape Memory Alloy ◽  
Shape Memory ◽  
X Ray Diffraction ◽  
Scanning Calorimetry ◽  
X Ray ◽  
One Step ◽  
Niti Matrix ◽  
Electronic Microscope

The nanocrystal, phase transformation and microstructure behavior of Ni50Ti50 shape memory alloy was investigated by scanning electronic microscope, X-ray diffraction and differential scanning calorimetry. The results showed that the microstructure of Ni-Ti binary alloy consists of the NiTi2 phase and the NiTi matrix phase. One-step phase transformation was observed alloy.

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.

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.

Darstellung und magnetische Eigenschaften einiger kristalliner Nitroxidradikale/Synthesis and Magnetic Properties of Some Crystalline Nitroxide Radicals

2000 ◽  
Vol 55 (7) ◽  
pp. 567-575 ◽  
Author(s):  
K. Griesar ◽  
E. A. Soto-Bustamante ◽  
W. Haase
Keyword(s):  
Differential Scanning Calorimetry ◽  
Magnetic Properties ◽  
Exchange Interactions ◽  
Antiferromagnetic Exchange ◽  
X Ray Diffraction ◽  
Temperature Dependent ◽  
Nitroxide Radicals ◽  
Scanning Calorimetry ◽  
Polarizing Microscopy ◽  
X Ray

Abstract The syntheses of different nitroxide radicals are reported. The thermal behaviour of the ni­ troxide radicals was examined by polarizing microscopy, differential scanning calorimetry as well as X-ray diffraction experiments. Temperature dependent magnetic susceptibility mea­surements were carried out in order to determine the magnetic properties of these nitroxide radicals. The majority of the radicals presented here show weak antiferromagnetic exchange interactions.

scholarly journals Structure, Microstructure, and Magnetic Properties of Melt Spun Ni50Mn50−xInx Ribbons

2021 ◽  
Vol 7 (5) ◽  
pp. 63
Author(s):  
Karima Dadda ◽  
Safia Alleg ◽  
Joan Saurina ◽  
Lluïsa Escoda ◽  
Joan-Josep Suñol
Keyword(s):  
Magnetic Properties ◽  
Thermal Hysteresis ◽  
Equilibrium Temperature ◽  
Indium Content ◽  
Martensitic Transition ◽  
X Ray Diffraction ◽  
Scanning Calorimetry ◽  
X Ray ◽  
Xrd Patterns ◽  
Microstructure And Magnetic Properties

Structural, microstructural, and magnetic properties of Heusler Ni50Mn50−xInx (x = 5 and 10) ribbons have been investigated by X-ray diffraction (XRD), scanning electron microscopy (SEM) coupled with energy dispersive X-ray spectroscopy (EDS), differential scanning calorimetry (DSC), and vibrating sample magnetometry (VSM). The as quenched Ni50Mn45In5 ribbons exhibit a mixture of monoclinic 14M (a = 4.329(3) Å, b = 5.530(3) Å, and c = 28.916(3) Å), and tetragonal L10 (a = b = 3.533(3) Å, and c = 7.522(3) Å) martensite structures, while Ni50Mn40In10 ribbons display a single monoclinic 14M phase (a = 4.262(3) Å, b = 5.692(3) Å, and c = 29.276(3) Å). After three heating/cooling cycles, in the temperature range of 303–873 K, the Rietveld refinement of the XRD patterns revealed the presence of a single 14M martensite for Ni50Mn45In5 ribbons, and a mixture of cubic L21 (31%) and 14M (69%) phases for Ni50Mn40In10 ribbons. The characteristic temperatures of the martensitic transition (Astart, Afinish, Mstart, and Mfinish), the thermal hysteresis temperature width, and the equilibrium temperature decreased with increasing indium content and heating cycles. The samples show a paramagnetic like behavior in the as quenched state, and a ferromagnetic like behavior after the third heating/cooling cycle.

Y-Type Hexaferrites: Structural, Dielectric and Magnetic Properties

2012 ◽  
Vol 189 ◽  
pp. 209-232 ◽  
Author(s):  
Rajshree B. Jotania ◽  
Hardev Singh Virk
Keyword(s):  
Magnetic Properties ◽  
Quantum Interference ◽  
Room Temperature ◽  
Structural Changes ◽  
Ferromagnetic State ◽  
X Ray Diffraction ◽  
Scanning Calorimetry ◽  
X Ray ◽  
Lcr Meter ◽  
Co Precipitation

This paper attempts to provide a historical survey of structure of various types of hexaferrites. It provides information about synthesis, characterization, structural, magnetic and dielectric properties of Y-type hexagonal ferrites using various chemical routes. We have prepared a series of cobalt doped Sr2Cu2-xCoxFe12O22(x = 0.0 to 1.0) hexaferrites using a wet chemical co-precipitation technique. The prepared hexaferrite precursors were calcined at 950 °C for 4 hours in a furnace and slowly cooled to room temperature. The crystal structure of Y-type hexaferrites is rather complicated. The chemical and structural changes were examined in detail by X-ray diffraction (XRD), Differential scanning calorimetry (DSC), Scanning electron microscopy (SEM), and Fourier transform infra-red (FTIR) spectroscopy. X-ray diffraction studies showed that sintering temperature as low as 950°C was sufficient to produce a single-phase Y-type hexaferrite material. The dielectric measurements were carried out over the frequency range of 100 Hz to 2 MHz at room temperature using an LCR meter to study the variation of dielectric constant and loss tangent with frequency. The magnetic properties of hexaferrite samples were investigated using a vibration sample magnetometer (VSM), and a superconducting quantum interference device (SQUID) magnetometer in the temperature range 30K to 200K. A change from ferromagnetic state to super paramagnetic state has been observed in Co doped Sr2Cu2-xCoxFe12O22(x= 0.6 to 1.0) hexaferrite. The novel applications of all types of hexaferrite materials have been described.

scholarly journals Structural, Thermal and Magnetic Properties of Ga Excess Ni-Mn-Ga

2009 ◽  
Vol 635 ◽  
pp. 43-47 ◽  
Author(s):  
Sanjay Singh ◽  
S. Bhardwaj ◽  
A.K. Panda ◽  
V.K. Ahire ◽  
Amitava Mitra ◽  
...  
Keyword(s):  
Differential Scanning Calorimetry ◽  
Magnetic Properties ◽  
Transition Temperature ◽  
Martensitic Transition ◽  
Martensitic Structure ◽  
X Ray Diffraction ◽  
Scanning Calorimetry ◽  
X Ray ◽  
Ga Doping ◽  
Heat Of Transformation

The martensitic transition and the ferro- to paramagnetic transition have been studied in a series of Ga excess Ni-Mn-Ga specimens [Ni2-xMnGa1+x (0.4≤ x≤ 0.9)] by differential scanning calorimetry and magnetization measurements. The martensitic transition exhibits a hysteresis whose width is similar to Ni2MnGa, indicating that the transition is thermoelastic. The latent heat of transformation is comparable with other Ni-Mn-Ga alloys. A substantial increase in the martensitic transition temperature is observed due to Ga doping. Interestingly, the x-ray diffraction pattern of all the compositions studied show a modulated martensitic structure in the martensitic phase.

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.

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