Microstructural evolution of Al–Fe powder mixtures during high-energy ball milling

1998 ◽  
Vol 33 (10) ◽  
pp. 2519-2527 ◽  
Author(s):  
F Cardellini ◽  
V Contini ◽  
R Gupta ◽  
G Mazzone ◽  
A Montone ◽  
...  
Keyword(s):  
Ball Milling ◽  
Microstructural Evolution ◽  
High Energy ◽  
High Energy Ball Milling ◽  
Powder Mixtures ◽  
Fe Powder ◽  
Energy Ball

X-ray diffraction study of microstructural evolution of some ZrO2–Y2O3–MgO powder mixtures induced by high-energy ball milling

2004 ◽  
Vol 379 (1-2) ◽  
pp. 216-221 ◽  
Author(s):  
Nada Stubičar ◽  
Vladimir Bermanec ◽  
Mirko Stubičar ◽  
Darko Popović ◽  
Wolfgang A. Kaysser
Keyword(s):  
Diffraction Study ◽  
Ball Milling ◽  
Microstructural Evolution ◽  
High Energy ◽  
High Energy Ball Milling ◽  
X Ray Diffraction ◽  
Powder Mixtures ◽  
X Ray ◽  
Energy Ball

An Investigation on the Mechanical Alloying of TiFe Compound by High-Energy Ball Milling

2010 ◽  
Vol 660-661 ◽  
pp. 329-334 ◽  
Author(s):  
Railson Bolsoni Falcão ◽  
Edgar Djalma Campos Carneiro Dammann ◽  
Cláudio José da Rocha ◽  
Ricardo Mendes Leal Neto
Keyword(s):  
Ball Milling ◽  
High Energy ◽  
High Energy Ball Milling ◽  
Low Density Polyethylene ◽  
Low Density ◽  
Powder Mixtures ◽  
Milling Parameters ◽  
Process Route ◽  
Partial Formation ◽  
Energy Ball

This work reports the efforts to obtain TiFe intermetallic compound by high-energy ball milling of Ti and Fe powder mixtures. This process route has been used to provide a better hydrogen intake in this compound. Milling was carried out in a SPEX mill at different times. Strong adherence of material at the vial walls was seen to be the main problem at milling times higher than 1 hour. Attempts to solve this problem were accomplished by adding different process control agents, like ethanol, stearic acid, low density polyethylene, benzene and cyclohexane at variable quantities and keeping constant other milling parameters like ball to powder ration and balls size. Better results were attained with benzene and cyclohexane, but with partial formation of TiFe compound even after a heat treatment (annealing) of the milled samples.

Structure and Thermal Stability of Nanostructured Iron-doped Zirconia Prepared by High-energy Ball Milling

1999 ◽  
Vol 14 (4) ◽  
pp. 1343-1352 ◽  
Author(s):  
J. Z. Jiang ◽  
F. W. Poulsen ◽  
S. Mørup
Keyword(s):  
Ball Milling ◽  
Unit Cell Volume ◽  
High Energy ◽  
High Energy Ball Milling ◽  
Iron Ions ◽  
Monoclinic Zirconia ◽  
Maximum Solubility ◽  
Powder Mixtures ◽  
Energy Ball ◽  
Thermal Stability Of

Fully stabilized cubic zirconia doped with iron oxide has been synthesized by high-energy ball milling from powder mixtures of monoclinic zirconia and hematite. It is found that the iron ions dissolved in cubic ZrO2 are in substitutional positions with a maximum solubility of approximately 18.5 mol% α–Fe2O3. The unit-cell volume of the cubic ZrO2 phase decreases with increasing iron content. During heating the cubic-to-tetragonal transition occurs at approximately 827 °C and the tetragonal-to-monoclinic transition seems to be absent at temperatures below 950 °C. During cooling the tetragonal-to-monoclinic transition occurs at 900–1100 °C.

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.

High energy ball milling of titania and titania–ceria powder mixtures

2014 ◽  
Vol 254 ◽  
pp. 591-596 ◽  
Author(s):  
Erika Furlani ◽  
Eleonora Aneggi ◽  
Carla de Leitenburg ◽  
Stefano Maschio
Keyword(s):  
Ball Milling ◽  
High Energy ◽  
High Energy Ball Milling ◽  
Powder Mixtures ◽  
Energy Ball
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