scholarly journals Experimental investigation on the formation mechanism of the TiFe alloy by the molten-salt electrolytic titanium concentrate

2011 ◽  
Vol 47 (2) ◽  
pp. 99-104 ◽  
Author(s):  
R. Shi ◽  
C. Bai ◽  
M. Hu ◽  
X. Liu ◽  
J. Du

The ferrotitanium alloy was prepared in the molten CaCl2 system, in which resolidified ilmenite and the graphite crucible were used as cathode and anode. In this study, the electrolytic voltage was fixed at 3.1V, and three different temperatures were applied: 850oC, 875oC and 900?C. Finally, the product was examined by SEM and XRD to determine the phase transformation after the electrolysis. The results show that the ilmenite was firstly reduced to Fe, and finally the TiFe alloy was formed. The intermediate products include CaTiO3, TiO2, Ti2O3, TiO, Fe, TiFe2, and Ti. Different product and structure can be obtained by changing temperature. According to thermodynamic calculation, the principal electroreduction products are Ti and TiFe2 and then Ti and TiFe2 are formed by interdiffusion which is governed by temperature.

2014 ◽  
Vol 35 (6) ◽  
pp. 606-614 ◽  
Author(s):  
Xiaoping Yang ◽  
Xiaoxi Yang ◽  
Frank G.F. Qin ◽  
Runhua Jiang

2009 ◽  
Vol 45 (1) ◽  
pp. 101-109 ◽  
Author(s):  
T.P. Jose ◽  
L. Sundar ◽  
L.J. Berchmans ◽  
A. Visuvasam ◽  
S. Angappan

Barium hexaboride (BaB6) crystals were electrochemically synthesized using molten salt technique. Barium carbonate (BaCO3) and boron trioxide (B2O3) was used as reactants. Lithium fluoride (LiF) was used as the supporting electrolyte. The molten electrolyte consisted of 50 wt % BaCO3 and B2O3 with different stiochiometric ratios of Ba and B and 50 wt % lithium fluoride. DTA/TGA studies were made to determine the eutectic point of the melt and it was found to be around 821oC. The electrolytic cell had a high purity graphite crucible, which served as the electrolyte holding vessel and also as the anode for the electrolysis. An electro-polished molybdenum rod was employed as the cathode. The electrolysis was performed at 870?C under argon atmosphere, at current densities ranging from 0.2-0.5 A/cm2. The electrodeposited crystals were examined for the phase identification using X-ray diffraction technique. The AAS and the chemical analysis were made for the determination of chemical composition of the synthesized crystals. The purity of the crystals was also assessed using ICP-MS, XRF and EDX, which reveal that the crystals were associated with trace amount of impurities like oxygen, carbon and iron. The compound is found to be more than 99 % pure. The morphology of the crystals was examined using Scanning Electron Microscopy (SEM). From the above studies, it is concluded that the molten salt process is a simple preparative procedure for the synthesis of sub-micron size barium hexaboride crystals.


Author(s):  
Kazuto Mizutani ◽  
Takuya HOSHII ◽  
Hitoshi WAKABAYASHI ◽  
Kazuo TSUTSUI ◽  
Edward Yi Chang ◽  
...  

Abstract The effects of 1-nm-thick CeOx capping on 7.5-nm-thick Y-doped HfO2 films on the ferroelectric characteristics are investigated. From the ferroelectric characteristics of the samples annealed at different temperatures from 450 to 600oC and annealing durations, the time (τ) required to stabilize the ferroelectric phase at each temperature was shortened by the capping. The identical activation energy (Ea) of 2.65 eV for ferroelectric stabilization without and with capping suggests the same kinetics for phase transformation. However, an increase in the remnant polarization (Pr) was obtained. Only a few Ce atoms diffused into the underlying HfO2 film even after 600oC annealing. Ferroelectric switching tests revealed an improvement in endurance from 107 to 1010 by the capping, presumably owing to the suppression of conductive filament formation. Therefore, CeOx capping is effective in promoting the ferroelectric phase in HfO2 with high switching endurance.


Author(s):  
Kai Zhao ◽  
Jing Zhou Yang ◽  
Zhao Hui Huang ◽  
Ming Hao Fang ◽  
Yan Gai Liu

Calphad ◽  
2010 ◽  
Vol 34 (1) ◽  
pp. 98-104 ◽  
Author(s):  
Zhongxi Zhu ◽  
Xuping Su ◽  
Jianhua Wang ◽  
Changjun Wu ◽  
Yu Wu

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