scholarly journals Sintering Behavior and Hardness of Tungsten Prepared by Hard Metal Sludge Recycling Process without Ammonium Paratungstate

2022 ◽  
Vol 60 (1) ◽  
pp. 53-61
Author(s):  
Hanjung Kwon ◽  
Jung-Min Shin

In this paper, we suggest a novel recycling process for hard metal sludge that does not use ammonium paratungstate. Ammonia, which in the conventional recycling process is essential for removing sodium and crystallized tungstate, was not used in the novel process. Instead of ammonia, acid was used to remove the sodium and crystallized tungstate resulting in the formation of tungstic acid (H2WO4). Tungsten powders were successfully synthesized by hydrogen reduction of the tungstic acid through H2O decomposition, WO3 to WO2 reduction, and tungsten metal formation. The tungsten powders prepared from tungstic acid were spherical in shape and had a higher sintering density than the facet-shaped tungsten powders prepared from tungsten oxide. The spherical shape of the tungsten powders enhanced their sinterability and resulted in an increase in the size of grains. This is a result of the high diffusion rate of the atoms along the particle surfaces. Despite having a higher density, the hardness of the sintered tungsten was lower than that of tungsten from tungsten oxide. High energy milling effectively reduced grain size and improved hardness. The hardness of the tungsten prepared from milled tungstic acid was enhanced to a value (max. 471 HV) higher than the best previously reported value (389 HV). In sum, tungsten can be hardened, thereby improving its sinterability and reducing grain size, with tungstic acid prepared using the proposed recycling process.

2017 ◽  
Vol 727 ◽  
pp. 72-75 ◽  
Author(s):  
Xiao Ming Fu

Fine tungsten powder is prepared with blue tungsten oxide (BTO) through the hydrogen reduction. The samples were characterized with the scanning electron microscope (SEM), fisher sub-sieve sizer (FSSS) and the particulate size description analyzer (PSDA). Fine tungsten powder is easily obtained when the reduction temperature is low. With the increasement of the reduction temperature, the grain size of tungsten powder becomes coarse. The increase of the weight of BTO in the ceramic boat leads to the increasement of the thickness of its bed. Therefore, the weight of BTO in the ceramic boat ought to reduce if fine tungsten powder is prepared. Fine tungsten powder can be obtained when the hydrogen flow increases.


2011 ◽  
Vol 2011 ◽  
pp. 1-5 ◽  
Author(s):  
Tae-Wan Kim ◽  
In-Yong Ko ◽  
Jung-Mann Doh ◽  
Jin-Kook Yoon ◽  
In-Jin Shon

A nanopowder ofFe3Alwas synthesized from 3Fe and Al by high-energy ball milling. A dense nanostructuredFe3Alwas consolidated by pulsed current activated sintering method within 2 minutes from mechanically synthesized powders ofFe3Aland horizontally milled powders of 3Fe+Al. The grain size, sintering behavior, and hardness ofFe3Alsintered from horizontally milled 3Fe+Al powders and high-energy ball milledFe3Alpowder were compared.


2010 ◽  
Vol 2010 ◽  
pp. 1-16 ◽  
Author(s):  
Yngve Bergström ◽  
Ylva Granbom ◽  
Dirk Sterkenburg

A dislocation model, accurately describing the uniaxial plastic stress-strain behavior of dual phase (DP) steels, is proposed and the impact of martensite content and ferrite grain size in four commercially produced DP steels is analyzed. It is assumed that the plastic deformation process is localized to the ferrite. This is taken into account by introducing a nonhomogeneity parameter, f(ε), that specifies the volume fraction of ferrite taking active part in the plastic deformation process. It is found that the larger the martensite content the smaller the initial volume fraction of active ferrite which yields a higher initial deformation hardening rate. This explains the high energy absorbing capacity of DP steels with high volume fractions of martensite. Further, the effect of ferrite grain size strengthening in DP steels is important. The flow stress grain size sensitivity for DP steels is observed to be 7 times larger than that for single phase ferrite.


2010 ◽  
Vol 654-656 ◽  
pp. 1106-1109
Author(s):  
Ya Qiong He ◽  
Chang Hui Mao ◽  
Jian Yang

Nanocrystalline Fe-Co alloy powders, which were prepared by high-energy mechanical milling, were nitrided under the mixing gas of NH3/H2 in the temperature range from 380°C to 510°C. X-ray diffraction (XRD) was used to analyze the grain size and reaction during the processing. The magnetic properties of the nitrided powders were measured by Vibrating Sample Magnetometer (VSM). The results show that with the appearance of Fe4N phase after nitride treatment, and the grain-size of FeCo phase decreases with the increase of nitridation temperature between 380°C to 450°C.The saturation magnetization of nitrided alloy powder treated at 480°C is about 18% higher than that of the initial Fe-Co alloy powder, accompanied by the reduction of the coercivity. Transmission electron microscope (TEM) was used, attempting to further analyze the effect of Fe4N phase on microstructure and magnetic properties of the powder mixtures.


2007 ◽  
Vol 534-536 ◽  
pp. 1389-1392
Author(s):  
Young Jung Lee ◽  
Baek Hee Lee ◽  
Gil Su Kim ◽  
Kyu Hwan Lee ◽  
Young Do Kim

Magnetic properties of nanostructured materials are affected by the microstructures such as grain size (or particle size), internal strain and crystal structure. Thus, it is necessary to study the synthesis of nanostructured materials to make significant improvements in their magnetic properties. In this study, nanostructured Fe-20at.%Co and Fe-50at.%Co alloy powders were prepared by hydrogen reduction from the two oxide powder mixtures, Fe2O3 and Co3O4. Furthermore, the effect of microstructure on the magnetic properties of hydrogen reduced Fe-Co alloy powders was examined using XRD, SEM, TEM, and VSM.


2007 ◽  
Vol 29-30 ◽  
pp. 143-146 ◽  
Author(s):  
Aamir Mukhtar ◽  
De Liang Zhang ◽  
C. Kong ◽  
P. R. Munroe

Cu-(2.5 or 5.0vol.%)Al2O3 nanocomposite balls and granules and Cu-(2.5vol.% or 5.0vol.%)Pb alloy powder were prepared by high energy mechanical milling (HEMM) of mixtures of Cu and either Al2O3 or Pb powders. It was observed that with the increase of the content of Al2O3 nanoparticles from 2.5vol.% to 5vol.% in the powder mixture, the product of HEMM changed from hollow balls into granules and the average grain size and microhardness changed from approximately 130nm and 185HV to 100nm and 224HV, respectively. On the other hand, HEMM of Cu–(2.5 or 5.0vol.%) Pb powder mixtures under the same milling conditions failed to consolidate the powder in-situ. Instead, it led to formation of nanostructured fine powders with an average grain size of less than 50nm. Energy dispersive X-ray mapping showed homogenous distribution of Pb in the powder particles in Cu–5vol.%Pb alloy powder produced after 12 hours of milling. With the increase of the Pb content from 2.5 to 5.0 vol.%, the average microhardness of the Cu-Pb alloy powder particles increases from 270 to 285 HV. The mechanisms of the effects are briefly discussed.


2021 ◽  
Vol 0 (0) ◽  
Author(s):  
Bambar Davaasuren ◽  
Qianli Ma ◽  
Alexandra von der Heiden ◽  
Frank Tietz

Abstract Li1.5Al0.5Ti1.5(PO4)3 (LATP) powders were prepared from different NO x -free precursors using an aqueous-based solution-assisted solid-state reaction (SA-SSR). The sintering behavior, phase formation, microstructure and ionic conductivity of the powders were explored as a function of sintering temperature. The powders showed a relatively narrow temperature windows in which shrinkage occurred. Relative densities of 95% were reached upon heating between 900 and 960 °C. Depending on the morphological features of the primary particles, either homogeneous and intact microstructures with fine grains of about <2 µm in size or a broad grain size distribution, micro-cracks and grain cleavages were obtained, indicating the instability of the microstructure. Consequently, the ceramics with a homogeneous microstructure possessed a maximum total ionic conductivity of 0.67 mS cm−1, whereas other ceramics reached only 0.58 mS cm−1 and 0.21 mS cm−1.


Sign in / Sign up

Export Citation Format

Share Document