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Materials-Metals 2017

Page 40

November 16-17, 2017 Paris, France

13

th

Annual Conference on

Materials Science, Metal and Manufacturing

Journal of Materials Science and Nanotechnology

Volume 1 Issue 2

Electrochemical fabrication of V-4Cr-4Ti alloys

from the mixed oxides in a eutectic CaCl

2

-NaCl

melt

Xiaozhou Cao

1,2

, Qiuyue Li

1,2

, Yuanyuan Shi

3

, He Yang

1,2

, Tao Jiang

1,2

and

Xiangxin Xue

1,2

1

Northeastern University, China

2

Key Laboratory of Recycling Science for Metallurgical Resource, China

3

Chinalco Shenyang Non-ferrous Metal Processing Co., Ltd, China

V

-4Cr-4Ti alloys exhibit important advantages as a

candidate structural material for fusion reactor first-wall

and blanket applications. V-4Cr-4Ti alloys were prepared

by direct electrochemical reduction of the solid mixture

of V

2

O

3

, Cr

2

O

3

and TiO

2

in molten CaCl

2

-NaCl melt at

1073K. The influence of cell voltage and electrolysis time on

the electrolysis process was reported. The microstructure

and phase compositions of the products were analyzed by

scanning electron microscopy (SEM) and X-ray diffraction

(XRD) during the electrolysis process. The results showed

that V-4Cr-4Ti alloys can be obtained at the voltage of 3.1V

and the time of 0.5h. The reduction process involved Cr

2

O

3

was reduced to Cr metal firstly, thereafter V

2

O

3

and TiO

2

was

reduced to low-valence oxide of vanadium and titanium.

The reduction rate increases with increasing cell voltage, lots

of perovskite oxide formed during the electrolysis process.

With the increase of the voltage, electrochemical reduction

rate increased on the surface of electrode, the current rapidly

decreased, and finally reached a stable value at a short time,

which is beneficial to accelerate the transferring of oxygen

ions. With the increase of time, the particles size of new

generated product is less than1μm after 120min of electrolysis

it becomes smaller and uniform.

Figure 1:

XRD patterns of the products at different electrolysis

time.

Figure 2:

Current-time plots of electro-deoxidation oxide

mixture at different electrolytic voltage.

Recent Publications

• Barabash V, Federici G, Linke J, Wu C H (2003) Material/

plasma surface interaction issues following neutron

damage. Journal of Nuclear Materials. 313-316:42-51.

• Xiao W, Wang D H (2014) The electrochemical reduction

processes of solid compounds in high temperaturemolten

salts. Chemical Social Reviews. 43(10):3215-3228.

• Kar P, Evans J W (2008) A model for the electrochemical

reduction of metal oxides in molten salt electrolyte.

Electrochimica Acta 54:835-843.

• Juzeliunas E, Cox A, Fray D J (2012) Electro-deoxidation

of thin silica layer in molten salt-Globular structures

with effective light absorbance. Electrochimica Acta

68:123-127.

• Alexander D T L, Schwandt C, Fray D J (2011) The

electro-deoxidation of dense titanium dioxide precursors

in molten calcium chloride giving a new reaction

pathway. Electrochimica Acta.56:3286-3295.

Biography

Xiaozhou Cao received his BS in 2003, MS and PhD degrees in 2008 with

Professor Zhuxian Qiu from Institute of Nonferrous Metallurgy at Northeastern

University. He joined the Institute of Metallurgical Resources and Environmental

Engineering at Northeastern University since 2008. His current research

focuses on molten salt and ionic liquid electrochemistry to seek a simple and

environmentally friendly way to produce the corresponding parent metals and

alloys.

caoxz@smm.neu.edu.cn

Xiaozhou Cao et al., Mater Sci Nanotechnol 2017, 1:2