Disordering and Reordering Kinetics of a Fe–40A1 B2 Alloy

1994 ◽  
Vol 364 ◽  
Author(s):  
S. Gialanella ◽  
M. D. Baró ◽  
L. Lutterotti ◽  
S. Suriñach
Keyword(s):  
Magnetic Measurements ◽  
High Energy ◽  
Defect Structures ◽  
X Ray Diffraction ◽  
High Concentration ◽  
Scanning Calorimetry ◽  
X Ray ◽  
Energy Ball ◽  
Heating Up ◽  
Kinetics Of

AbstractThe ordered structure of Fe–40A1 B2 powders was completely disordered by high energy ball-milling. The defect structures of the powders disordered to different extents were characterized using X-Ray diffraction. A significant lattice expansion was observed, which we tried to relate to the high concentration of point defects introduced into the material as a consequence of milling.A complete reordering was accomplished by heating up the specimens under an inert Ar atmosphere. We followed the kinetics of the disorder to order transformation by Differential Scanning Calorimetry and Thermogravimetric Magnetic Measurements. The two techniques allowed us to identify the temperature range and the apparent activation energy of the process. As expected, a decrease in the magnetic moment of the originally disordered powders as a consequence of the reordering treatments was also observed.

Microstructural Transformations of an Amorphous Fe90 Zr10 Alloy Induced by High-Energy Ball-Milling

2006 ◽  
Vol 510-511 ◽  
pp. 698-701
Author(s):  
Pyuck Pa Choi ◽  
Young Soon Kwon ◽  
Ji Soon Kim ◽  
Dae Hwan Kwon
Keyword(s):  
Ball Milling ◽  
Milling Time ◽  
High Energy ◽  
High Energy Ball Milling ◽  
X Ray Diffraction ◽  
Scanning Calorimetry ◽  
X Ray ◽  
Melt Spun ◽  
Energy Ball ◽  
Induced Crystallization

Mechanically induced crystallization of an amorphous Fe90Zr10 alloy was studied by means of X-ray diffraction (XRD) and differential scanning calorimetry (DSC). Under high-energy ball-milling in an AGO-2 mill, melt-spun Fe90Zr10 ribbons undergo crystallization into BCC α- Fe(Zr). Zr atoms are found to be solved in the Fe(Zr) grains up to a maximum supersaturation of about 3.5 at.% Zr, where it can be presumed that the remaining Zr atoms are segregated in the grainboundaries. The decomposition degree of the amorphous phase increases with increasing milling time and intensity. It is proposed that the observed crystallization is deformation-induced and rather not attribute to local temperature rises during ball-collisions.

Hydrogen Desorption/Absorption Kinetics of MgH2 Catalyzed with TiO2

2014 ◽  
Vol 986-987 ◽  
pp. 88-91
Author(s):  
Yan Wang ◽  
Shi Wei Wu ◽  
Hao Yu ◽  
Na Na Gong ◽  
Zhong Qiu Cao ◽  
...  
Keyword(s):  
Milling Time ◽  
Hydrogen Desorption ◽  
High Energy ◽  
Absorption Kinetics ◽  
Orthorhombic Structure ◽  
X Ray Diffraction ◽  
X Ray ◽  
Milled Sample ◽  
Energy Ball ◽  
Kinetics Of

We report on the preparation and hydrogen desorption/absorption kinetics of nanocrystalline magnesium hydride (MgH2) added commercial TiO2by high-energy ball milling. The phase and composition of the as-milled powders are characterized by X-ray diffraction (XRD). The results show that the milled sample contained MgH2phase, small amount of Mg and various phases of TiO2such as tetragonal and orthorhombic structure. The effect of the milling time (10, 20 and 30 h) on the hydrogen desorption property of MgH2has been investigated and found that the milling time of 20 h has excellent dehydrogenation properties, which can release 3.3 wt% H2within 60 min at 300oC, which indicates that the kinetics of hydrogen desorption of MgH2-TiO2composite has been greatly enhanced compared to the pure MgH2. Moreover, hydrogen absorption kinetics of the sample milled 20 h has been studied and the hydrogen content is 0.7, 0.8 and 1.2 wt% H2at 250, 280 and 300oC within 60 min, respectively.

Study of Obtainment of NiCrAlC Alloys by High Energy Ball Milling

2012 ◽  
Vol 727-728 ◽  
pp. 190-194 ◽  
Author(s):  
Joéverton I. Pereira ◽  
Alisson K. da Silva ◽  
Selauco Vurobi Jr. ◽  
José Deodoro Trani Capochi ◽  
Osvaldo Mitsuyuki Cintho
Keyword(s):  
Nickel Alloys ◽  
High Energy ◽  
X Ray Diffraction ◽  
Scanning Calorimetry ◽  
Energy Dispersion Spectroscopy ◽  
Chromium Carbides ◽  
X Ray ◽  
Gamma Prime ◽  
Energy Ball ◽  
Prime Phase

This work aims the synthesis of nickel alloys (Ni-Cr-Al-C) with different amounts of carbon, in order to measure the hardness and analyze the chromium carbides distribution and size, as well as for gamma prime phase. It has been used the mechanical alloying technique in order to provide a fine dispersion of chromium carbides in the gamma prime phase matrix. The materials were characterized by x-ray diffraction, differential scanning calorimetry, scanning electron microscopy, energy dispersion spectroscopy, and microhardness test.

Catalytic Effect of Ti on H-Desorption/Absorption Properties in MgH2 Prepared by Ball Milling

2014 ◽  
Vol 687-691 ◽  
pp. 4335-4338
Author(s):  
Yan Wang
Keyword(s):  
Ball Milling ◽  
Milling Time ◽  
Hydrogen Desorption ◽  
High Energy ◽  
X Ray Diffraction ◽  
Absorption Properties ◽  
X Ray ◽  
Milled Sample ◽  
Energy Ball ◽  
Kinetics Of

We report on the preparation and hydrogen desorption/absorption kinetics of nanocrystalline magnesium hydride (MgH2) added commercial Ti by high-energy ball milling. The phase and composition of the as-milled powders are characterized by X-ray diffraction (XRD). The results show that the milled sample contained MgH2phase, Ti phase and small amount of MgO phase. When the milling time is 30 h, the hydrogen desorption property of MgH2has been investigated and found that the sample releases 0.43, 0.86 and 0.90 wt% H2in 200 minutes at 280, 290 and 300oC , respectively. Moreover, the sample absorbs 0.48, 0.0.58 and 0.61 wt% H2in 15 minutes at 280, 290 and 300oC , respectively. It can be seen that the kinetics of hydrogen desorption/absorption of MgH2-Ti composite has been greatly enhanced compared to the pure MgH2.

Synthesis, Magnetic and Mössbauer Studies of Mechanically Alloyed Fe0.63Si0.37 Alloys

2006 ◽  
Vol 514-516 ◽  
pp. 1265-1268
Author(s):  
Benilde F.O. Costa ◽  
Vitor S. Amaral ◽  
Gerard Le Caër ◽  
Gerard Le Caër
Keyword(s):  
Magnetic Measurements ◽  
High Energy ◽  
Alloy Formation ◽  
X Ray Diffraction ◽  
Mechanically Alloyed ◽  
X Ray ◽  
Saturation Magnetic Moment ◽  
Spectral Components ◽  
Energy Ball ◽  
Fesi Alloy

Elemental powder mixtures of Fe and Si were mechanically alloyed with a ball-mill. Mössbauer spectroscopy and X-ray diffraction were used to characterise the microstructural changes of these mixtures which are induced by high-energy ball-milling. Mössbauer spectra are discussed in terms of two main spectral components (corresponding to FeSi alloy and α-Fe) and the time dependence of the alloy formation follows a Johnson-Mehl type law. Calorimetry measurements show that the formed alloy is stable up to 800°C as no crystallisation or phase transformation peaks are observed. From X-ray diffraction, a crystallite size of 9 nm is obtained. Magnetic measurements at low temperature were carried out on the final alloy and the saturation magnetic moment at 4.2K is 0.44 μB/Fe.

scholarly journals Leaching Titaniferous Magnetite Concentrate by Alkaline Aqueous Solution

2021 ◽  
Author(s):  
Ke Guo ◽  
Shaoyan Wang ◽  
Renfeng Song ◽  
Zhiqiang Zhang
Keyword(s):  
Aqueous Solution ◽  
Alkali Concentration ◽  
Water Usage ◽  
X Ray Diffraction ◽  
High Concentration ◽  
X Ray ◽  
Iron Concentrate ◽  
Titaniferous Magnetite ◽  
Magnetite Concentrate ◽  
Kinetics Of

AbstractLeaching titaniferous magnetite concentrate with alkali solution of high concentration under high temperature and high pressure was utilized to improve the grade of iron in iron concentrate and the grade of TiO2 in titanium tailings. The titaniferous magnetite concentrate in use contained 12.67% TiO2 and 54.01% Fe. The thermodynamics of the possible reactions and the kinetics of leaching process were analyzed. It was found that decomposing FeTiO3 with NaOH aqueous solution could be carried out spontaneously and the reaction rate was mainly controlled by internal diffusion. The effects of water usage, alkali concentration, reaction time, and temperature on the leaching procedure were inspected, and the products were characterized by X-ray diffraction, scanning electron microscope, and energy dispersive spectroscopy, respectively. After NaOH leaching and magnetic separation, the concentrate, with Fe purity of 65.98% and Fe recovery of 82.46%, and the tailings, with TiO2 purity of 32.09% and TiO2 recovery of 80.79%, were obtained, respectively.

Study in performance and morphology of polyamide 12 produced by selective laser sintering technology

2018 ◽  
Vol 24 (5) ◽  
pp. 813-820 ◽  
Author(s):  
Junjie Wu ◽  
Xiang Xu ◽  
Zhihao Zhao ◽  
Minjie Wang ◽  
Jie Zhang
Keyword(s):  
Selective Laser Sintering ◽  
Polarized Light ◽  
Chain Scission ◽  
High Energy ◽  
Laser Sintering ◽  
X Ray Diffraction ◽  
Scanning Calorimetry ◽  
Content Type ◽  
X Ray ◽  
Polyamide 12

Purpose The purpose of this paper is to investigate the effect of selective laser sintering (SLS) method on morphology and performance of polyamide 12. Design/methodology/approach Crystallization behavior is critical to the properties of semi-crystalline polymers. The crystallization condition of SLS process is much different from others. The morphology of polyamide 12 produced by SLS technology was investigated using scanning electron microscopy, polarized light microscopy, differential scanning calorimetry, X-ray diffraction and wide-angle X-ray diffraction. Findings Too low fill laser power brought about bad fusion of powders, while too high energy input resulted in bad performance due to chain scission of macromolecules. There were three types of crystal in the raw powder material, denoted as overgrowth crystal, ring-banded spherulite and normal spherulite. Originality/value In this work, SLS samples with different sintering parameters, as well as compression molding sample for the purpose of comparison, were made to study the morphology and crystal structure of sintered PA12 in detail.

Microstructure Evolution of a Fine Grain Al-50wt%Si Alloy Fabricated by High Energy Milling

2011 ◽  
Vol 479 ◽  
pp. 54-61 ◽  
Author(s):  
Fei Wang ◽  
Ya Ping Wang
Keyword(s):  
Grain Growth ◽  
Microstructure Evolution ◽  
Room Temperature ◽  
Milling Time ◽  
High Energy ◽  
X Ray Diffraction ◽  
Scanning Calorimetry ◽  
Laser Method ◽  
X Ray ◽  
Fine Grain

Microstructure evolution of high energy milled Al-50wt%Si alloy during heat treatment at different temperature was studied. Scanning electron microscope (SEM) and X-ray diffraction (XRD) results show that the size of the alloy powders decreased with increasing milling time. The observable coarsening of Si particles was not seen below 730°C in the high energy milled alloy, whereas, for the alloy prepared by mixed Al and Si powders, the grain growth occurred at 660°C. The activation energy for the grain growth of Si particles in the high energy milled alloy was determined as about 244 kJ/mol by the differential scanning calorimetry (DSC) data analysis. The size of Si particles in the hot pressed Al-50wt%Si alloy prepared by high energy milled powders was 5-30 m at 700°C, which was significantly reduced compared to that of the original Si powders. Thermal diffusivity of the hot pressed Al-50wt%Si alloy was 55 mm2/s at room temperature which was obtained by laser method.

scholarly journals Structural Evolution in Wet Mechanically Alloyed Co-Fe-(Ta,W)-B Alloys

Metals ◽  
2021 ◽  
Vol 11 (5) ◽  
pp. 800
Author(s):  
Vladimír Girman ◽  
Maksym Lisnichuk ◽  
Daria Yudina ◽  
Miloš Matvija ◽  
Pavol Sovák ◽  
...  
Keyword(s):  
Structural Changes ◽  
Magnetic Measurements ◽  
Structural Evolution ◽  
High Energy ◽  
Control Agent ◽  
X Ray Diffraction ◽  
Mechanically Alloyed ◽  
X Ray ◽  
Transmission Electron ◽  
X Ray Absorption

In the present study, the effect of wet mechanical alloying (MA) on the glass-forming ability (GFA) of Co43Fe20X5.5B31.5 (X = Ta, W) alloys was studied. The structural evolution during MA was investigated using high-energy X-ray diffraction, X-ray absorption spectroscopy, high-resolution transmission electron microscopy and magnetic measurements. Pair distribution function and extended X-ray absorption fine structure spectroscopy were used to characterize local atomic structure at various stages of MA. Besides structural changes, the magnetic properties of both compositions were investigated employing a vibrating sample magnetometer and thermomagnetic measurements. It was shown that using hexane as a process control agent during wet MA resulted in the formation of fully amorphous Co-Fe-Ta-B powder material at a shorter milling time (100 h) as compared to dry MA. It has also been shown that substituting Ta with W effectively suppresses GFA. After 100 h of MA of Co-Fe-W-B mixture, a nanocomposite material consisting of amorphous and nanocrystalline bcc-W phase was synthesized.

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