MECHANOCHEMICAL SYNTHESIS OF TIAL3/AL2O3 ULTRAFINE GRAINED COMPOSITE

2008 ◽  
Vol 22 (18n19) ◽  
pp. 2914-2923 ◽  
Author(s):  
M. M. VERDIAN ◽  
S. HESHMATI-MANESH

The TiAl 3/ Al 2 O 3 metal-ceramic composite was synthesized using high energy ball milling, powder compaction and thermal treatment. Micron sized powders of titanium oxide ( TiO 2) and aluminum were subjected to high energy ball milling under an argon protected atmosphere. Milling of this powder mixture although reduced crystallites sizes to a nano scale, did not result in a reaction between the reactants. Further compaction of the milled powder and annealing, paved the way to a reduction reaction and led to the formation of an ultrafine grained composite structure. The reaction appeared to proceed through two-steps. Titanium oxide was first reduced to TiO and later on, TiO was reduced to Ti . The resulting Ti was alloyed with extra Al to produce TiAl 3 intermetallic in which alumina particles were dispersed. Also, mechanical activation was found to reduce the reaction temperature between Al and TiO 2. The morphology and phase composition of the milling products were evaluated by scanning electron microscopy (SEM) and X-ray diffraction (XRD) analysis.

2013 ◽  
Vol 401-403 ◽  
pp. 635-638
Author(s):  
Ping Luo ◽  
Shi Jie Dong ◽  
Zhi Xiong Xie ◽  
Wei Yang ◽  
An Zhuo Yangli

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.


2018 ◽  
Vol 44 (6) ◽  
pp. 7291-7295 ◽  
Author(s):  
Xiaorong Zhang ◽  
Zhixiao Zhang ◽  
Bin Nie ◽  
Huanyu Chen ◽  
Guangshuo Wang ◽  
...  

2010 ◽  
Vol 660-661 ◽  
pp. 82-87 ◽  
Author(s):  
Felipe Antunes Santos ◽  
Alfeu Saraiva Ramos ◽  
Claudinei dos Santos ◽  
Paulo Atsushi Suzuki ◽  
Durval Rodrigues Júnior

The present study suggests the use of high energy ball milling to mix (to dope) the phase MgB2 with the AlB2 crystalline structure compound, ZrB2, with the same C32 hexagonal structure than MgB2, in different concentrations, enabling the maintenance of the crystalline phase structures practically unaffected and the efficient mixture with the dopant. The high energy ball milling was performed with different ball-to-powder ratios. The analysis of the transformation and formation of phases was accomplished by X-ray diffractometry (XRD), using the Rietveld method, and scanning electron microscopy. As the high energy ball milling reduced the crystallinity of the milled compounds, also reducing the size of the particles, the XRD analysis were influenced, and they could be used as comparative and control method of the milling. Aiming the recovery of crystallinity, homogenization and final phase formation, heat treatments were performed, enabling that crystalline phases, changed during milling, could be obtained again in the final product.


2006 ◽  
Vol 168 (1-3) ◽  
pp. 1057-1063 ◽  
Author(s):  
Ligia E. Zamora ◽  
G. A. Perez Alcazar ◽  
J. M. Greneche ◽  
S. Suriñach

2007 ◽  
Vol 353-358 ◽  
pp. 1625-1628 ◽  
Author(s):  
Gen Shun Ji ◽  
Qin Ma ◽  
Tie Ming Guo ◽  
Qi Zhou ◽  
Jian Gang Jia ◽  
...  

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.


2006 ◽  
Vol 510-511 ◽  
pp. 698-701
Author(s):  
Pyuck Pa Choi ◽  
Young Soon Kwon ◽  
Ji Soon Kim ◽  
Dae Hwan Kwon

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.


2016 ◽  
Vol 849 ◽  
pp. 844-851
Author(s):  
Juan Zhou ◽  
Yong Chen ◽  
Hong Mei Zhu ◽  
Xiang Fang Fan

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.


2007 ◽  
Vol 353-358 ◽  
pp. 1505-1508
Author(s):  
Zhi Hua Yang ◽  
Yu Zhou ◽  
De Chang Jia ◽  
Qing Chang Meng ◽  
Chang Qing Yu

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.


2011 ◽  
Vol 319-320 ◽  
pp. 61-63 ◽  
Author(s):  
Xiu Yan Guo ◽  
Guo Jin Ma ◽  
Shi Kun Xie ◽  
Rong Xi Yi ◽  
Zhi Gao

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.


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