Effect of High Energy Ball Milling on Structures and Properties of Atomization Fe-Based Nanocrystalline Soft Magnetic Powders

2016 ◽  
Vol 849 ◽  
pp. 844-851
Author(s):  
Juan Zhou ◽  
Yong Chen ◽  
Hong Mei Zhu ◽  
Xiang Fang Fan
Keyword(s):  
Ball Milling ◽  
High Energy ◽  
High Energy Ball Milling ◽  
Magnetic Alloy ◽  
X Ray Diffraction ◽  
Soft Magnetic ◽  
Soft Magnetic Alloy ◽  
Structures And Properties ◽  
Energy Ball ◽  
Saturation Magnetic Induction

The microstructure and strain of gas atomization and water collection Fe73Si3B24 soft magnetic alloy powder treated by high energy ball milling were investigated via SEM and X-ray diffraction. And the magnetic properties of those powders were studied via VSM (Vibrating Sample Magnetometer). The results show that the atomization powders almost exhibited spheric or ellipsoidal shape. The averaged particle size was 104.94 μm. The main phases were composed of α-Fe (Si) and amorphous phase. As ball milling time went on, the interplanar space, amount of amorphous and crystal microstrain of the powders increased, while the grain size decreased. The peak for the (110) crystal plane of α-Fe (Si) phase widened, while the peaks for (200), (211) crystal planes weakened. These three peaks shifted towards to small angle direction. The saturation magnetic induction of treated powders was steady, and the coercivity of samples increased.

Mössbauer, X-ray diffraction and magnetization studies of Fe–Mn–Al–Nb alloys prepared by high energy ball milling

2006 ◽  
Vol 168 (1-3) ◽  
pp. 1057-1063 ◽  
Author(s):  
Ligia E. Zamora ◽  
G. A. Perez Alcazar ◽  
J. M. Greneche ◽  
S. Suriñach
Keyword(s):  
Ball Milling ◽  
High Energy ◽  
High Energy Ball Milling ◽  
X Ray Diffraction ◽  
X Ray ◽  
Energy Ball

Nickel Silicides Synthesized by High Energy Ball Milling

2007 ◽  
Vol 353-358 ◽  
pp. 1625-1628 ◽  
Author(s):  
Gen Shun Ji ◽  
Qin Ma ◽  
Tie Ming Guo ◽  
Qi Zhou ◽  
Jian Gang Jia ◽  
...  
Keyword(s):  
Mechanical Alloying ◽  
Ball Milling ◽  
Milling Time ◽  
High Energy ◽  
Planetary Mill ◽  
High Energy Ball Milling ◽  
X Ray Diffraction ◽  
Microstructure Morphology ◽  
Energy Ball ◽  
Xrd Patterns

The high energy ball milling of Ni-50 atom % Si elemental powder mixtures was carried out using a planetary mill. X-ray diffraction (XRD) was used to identify the phase evolutions during the high energy ball milling period. The microstructure morphology of the powders milled different time was determined by field emission scanning electron microscope (FESEM). The beginning time of mechanical alloying was determined by back scattered electrons (BSE) images. The XRD patterns showed that the nickel peaks intensity and the silicon peaks intensity obviously decreased with milling time increased to 1 hour. BSE images revealed that nickel and silicon powders were not blended uniformly for 1 hour of milling. It was found that NiSi formed as the milling time increased to 5 hours, simultaneously, the nickel peaks and the silicon peaks almost disappeared. That means the obvious mechanical alloying started from 5 hours of milling. BSE images agreed with the result analyzed from XRD patterns. With the milling time further increased from 10 to 75 hours, the NiSi peaks decreased gradually, at the same time, the Ni2Si peaks appeared and then increased gradually.

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.

BBPPAmorphous Si-B-C-N Ceramics Fabricated by High Energy Ball Milling and Hot Pressing

2007 ◽  
Vol 353-358 ◽  
pp. 1505-1508
Author(s):  
Zhi Hua Yang ◽  
Yu Zhou ◽  
De Chang Jia ◽  
Qing Chang Meng ◽  
Chang Qing Yu
Keyword(s):  
Ball Milling ◽  
Hot Pressing ◽  
Hexagonal Boron Nitride ◽  
High Energy ◽  
High Energy Ball Milling ◽  
X Ray Diffraction ◽  
X Ray ◽  
Transmission Electron ◽  
Energy Ball ◽  
Amorphous Si

Amorphous Si-B-C-N ceramics obtained by high energy ball milling and hot pressing using hexagonal boron nitride (h-BN), graphite (C) and amorphous Si as starting materials have been studied. The mechanical milling with high energy resulted in the generation of large amounts of amorphous composites only milled for 5 h. Si-B-C-N powders were consolidation by hot pressing at 1850 °C. X-ray diffraction (XRD) and transmission electron microscopy (TEM) show that small amount of BN and SiC crystal lies in the amorphous matrix. The flexural strength reached the maximal value of 137.2 MPa at a mole ratio of BN/(Si+C) being 0.6.

Preparation of C/Cu Composite Powders by High-Energy Ball-Milling

2011 ◽  
Vol 319-320 ◽  
pp. 61-63 ◽  
Author(s):  
Xiu Yan Guo ◽  
Guo Jin Ma ◽  
Shi Kun Xie ◽  
Rong Xi Yi ◽  
Zhi Gao
Keyword(s):  
Ball Milling ◽  
Graphite Powder ◽  
High Energy ◽  
Lattice Parameter ◽  
High Energy Ball Milling ◽  
X Ray Diffraction ◽  
Composite Powders ◽  
Mixed Powder ◽  
X Ray ◽  
Energy Ball

Cu-4% mixed-powder consisting of rough copper powder and graphite powder was separately mechanical alloyed by high-energy ball milling. The phases and micrograph of these powders were determined by X-ray diffraction and scanning electron microscopy (SEM). The results show an increase in the lattice parameter of copper with milling times, up to a saturation value of about 24h; There was an absence of graphite reflections from X-ray diffractograms after longer milling times.

High Energy Ball-Milling of Tin Titanate Zirconate for Use in Microwave Applications

2006 ◽  
Vol 45 ◽  
pp. 480-485 ◽  
Author(s):  
V.L. Arantes ◽  
Dulcina P.F. Souza
Keyword(s):  
Particle Size ◽  
Dielectric Properties ◽  
Ball Milling ◽  
High Energy ◽  
Liquid Phase Sintering ◽  
High Energy Ball Milling ◽  
X Ray Diffraction ◽  
Microwave Frequencies ◽  
Particle Size Analyzer ◽  
Energy Ball

Tin titanate zirconate (ZTS) is widely known for its good dielectric properties at high frequencies and has been widely employed as a dielectric resonator. ZTS does not sinter easily by solid state difusion and it is necessary to introduce sintering aids capable of increasing diffusion coefficients and/or leading to liquid phase sintering. Consequently, the dielectric properties in microwave frequencies can be reduced. This work focused on the utilization of high energy ball-milling as a method of reducing initial particle size and further improving sintering of ZTS.The powders obtained were characterized by X-ray diffraction as a function of milling time, as well as by a light scattering particle size analyzer.

In Situ Synthesis of TiC-TiB2 Composites via High Energy Ball Milling and Pressureless Sintering

2013 ◽  
Vol 401-403 ◽  
pp. 635-638
Author(s):  
Ping Luo ◽  
Shi Jie Dong ◽  
Zhi Xiong Xie ◽  
Wei Yang ◽  
An Zhuo Yangli
Keyword(s):  
Ball Milling ◽  
Milled Powder ◽  
High Energy ◽  
High Energy Ball Milling ◽  
Sintering Process ◽  
Composite Ceramics ◽  
X Ray Diffraction ◽  
Powder Mixtures ◽  
Energy Ball

TiC-TiB2 composite ceramics were successfully fabricated via planetary ball milling of 72 mass% Ti and 28 mass % B4C powders, followed by low temperature sintering process at 1200°C. The microstructure of the ball-milled powder mixtures and composite ceramics were characterized by Differential thermal analysis equipment (DTA), field emission scanning electron microscopy (FESEM) and X-ray diffraction (XRD). The results showed that the ball-milled powder mixtures (Ti and B4C powders) were completely transformed to TiC-TiB2 composite ceramics as the powders were milled for 60 h and sintered at 1200°C for 1 h. The formation mechanism of the TiC-TiB2 composite was discussed. The high energy ball milling and necessary sintering for the powder mixtures plays an important role in the formation of the composites.

Structural and Microstructural Properties of Si-C and Si-C-B Powders Obtained by High-Energy Ball Milling

2016 ◽  
Vol 869 ◽  
pp. 19-24
Author(s):  
Lucas Moreira Ferreira ◽  
D.S. Mégda ◽  
A.C. de Souza ◽  
Rodrigo Fernando Costa Marques ◽  
Erika Coaglia Trindade Ramos ◽  
...  
Keyword(s):  
Ball Milling ◽  
Structural Modification ◽  
High Energy ◽  
High Energy Ball Milling ◽  
Fracture Mechanisms ◽  
Microstructural Properties ◽  
X Ray Diffraction ◽  
Powder Mixtures ◽  
X Ray ◽  
Energy Ball

This work evaluated on the structural modification during high-energy ball milling of the Si-50C, Si-42.9C-19.1B e Si-33.3C-44.4B (at.-%) powder mixtures from elemental powders. Electron images revealed on occurrence of continuous fracture mechanisms in brittle particles during their processing, which presented rounded particles lower than 10 μm. X-ray diffraction results of Si-50C powders indicated that the intensity of Si peaks was slightly reduced after milling for 17 h, which were moved to the direction of larger diffraction angles after 7 h of milling, suggesting that carbon atoms were dissolved into the Si lattice in order to form an extended solid solution. Following, these values were increased due to the discrete exothermic formation of the SiC compound. In Si-C-B powder mixtures, the SiC and B4C compounds were formed after milling for 7 h.

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