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  1. Home

Ni-doped Effects on Tungsten Copper Electrode

Category: Tungsten Information
Published on 09 December 2015

Except cobalt (Co) element, Nickel (Ni) is also a kind of common additives, and the density, the hardness, the electrical conductivity and other comprehensive properties of tungsten copper electrode will be influenced by the content of Ni. The effect of content of Ni on the density and hardness of tungsten copper W-25Cu electrode as follow:

tungsten copper electrode

The diagram shows that the density and the hardness of tungsten copper electrode is sensitive to the adding Ni element. When the content of Ni is 0.3%, the density rapidly increases 14.9g/cm3 to 17.0g/cm3. Therefore, adding Ni element will improve the density and the hardness of tungsten copper products.

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Mechannism and Operational Conditions of Silicon, Phosphrous, Arsenic Ammonium Paratungstate (APT)

Category: Tungsten Information
Published on 09 December 2015
Ammonium paratungstate (or APT) is a white crystalline salt of ammonium and tungsten, with the chemical formula (NH4)10(H2W12O42)·4H2O.
 
Ammonium paratungstate is produced by separating tungsten from its ore. Once the ammonium paratungstate is prepared, it is heated to its decomposition temperature, 600 °C. Left over is WO3, tungsten(VI) oxide. From there, the oxide is heated in an atmosphere of hydrogen, reducing the tungsten to elemental powder, leaving behind water vapor. From there, the tungsten powder can be fused into any number of things, from wire to bars to other shapes.

The study shows that the precipitation and the distribution ratio (C S/C L) of Si, P, As in solid and liquid phases decrease with the increase of the concentration of WO3 in the crystallization process of APT. With the increase of crystallization ratio of tungsten, the C S/C L ratio of Si, P, As increases first and decreases afterwards. The order of the amount of decrease is SiPAs. The Si, P As contents in APT decreases with the increase of the temperature and shortening of the crystallization time. The reduction of the relative surface area of crystallization tank benefits the decrease of As. The distributions ratio measured in the experiment were: As 0.11~0.37, P 0.10~0.26, Si 0.012~0.15. The theoretical analysis and experimental results showed that the entrainment of Si, P, As in APT in the first stage is possibly a replacement and the possibility of arsenate forms heteropolyacid with tungstate is higher than silicate and phosphorate in the middle stage of the crystallization of APT.

 

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The Average Particle Size of Ammonium Paratungstate Reducing Process

Category: Tungsten Information
Published on 09 December 2015
A process for reducing the average particle size of an ammonium paratungstate powder having the steps of heating the ammonium paratungstate powder at a temperature of between about 110° C to about 205° C for a time sufficient to reduce the average particle size of the ammonium paratungstate powder by at least 20 percent.
 
BACKGROUND
 
While a number of applications exist for ammonium paratungstate (APT) powders, a particularly important application is their use as a source material in the production of tungsten and tungsten carbide powders. In this regard, it is desirable to produce ammonium paratungstate powders having specific particle distributions to influence the size of the resultant metal and carbide powders. It is particularly advantageous to be able to produce small size APT powders (mean particle size less than 80 microns) for use in producing small metal and carbide grades (mean particle size between 0.5 to 2 microns).
 
APT can be made from a number of processes. The primary hydrometallurgical synthesis used involves the formation of a sodium tungstate solution. This solution can then be purified and converted into an ammonium tungstate solution which is then evaporated to yield ammonium paratungstate. The particle size of crystalline APT powders precipitated from solution can be reduced by milling the powder. However, the milling introduces unwanted contamination into the APT powder. Smaller seed crystals of APT can be added to the saturated solutions to induce the formation of smaller APT crystals but milling APT to produce the desired size for the seed crystals may still lead to contamination of the precipitated crystals. Thus, it would be desirable to be able to produce APT powders having the desired particle sizes without milling.
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Co-doped Effects on Tungsten Copper Electrode V

Category: Tungsten Information
Published on 08 December 2015

Since the large part of tungsten copper electrode is used for EDM (Electrical Discharge Machining), the measure of its electrical conductivity is crucial. However, the electrical conductivity is sensitive to the impurities and porosity so that the adding cobalt (Co) has an large effect on the electrical conductivity of tungsten copper electrode. The effect of different content of Co on the electrical conductivity of tungsten copper electrode diagram as follow:

tungsten copper electrode













The diagram shows that the adding Co element dramatically decreases the electrical conductivity of tungsten copper electrode. Before adding Co element, the electrical conductivity is about 34.5%IACS, while adds 0.2% Co element, the electrical conductivity greatly decreases 34.5%IACS to 16.4%IACS. With the constant increase of Co content, the electrical conductivity decrease constantly. However, tungsten dissolving in Co improves the sintering densification, a large number of solid phases connected with each other to form the continuous tungsten skeleton, the infiltration of liquid phase copper has been restricted, which leads to the maldistribution.

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Co-doped Effects on Tungsten Copper Electrode IV

Category: Tungsten Information
Published on 08 December 2015

Use cobalt (Co) powder as activator can greatly promote the solid phase sintering of tungsten skeleton. Some studies have shown that due to the existence of W6CO7 phase or Co atom on the surface of tungsten particle, it has better wettability and improve the rearrangements of particles in sintering. Although the effect of Co additives can not be removed, the high phase boundary diffusion and the transformation of material are enhancing. In the process of tungsten skeleton sintering, W dissolved in Co, firstly formed "carrier phase" on the surface of tungsten particle and then the tungsten atom by spreading the opposing Co phase, when liquid phase sintering is preferentially formed in connecting skeleton. Co-W and Co-Cu binary phase diagram as follow:

tungsten copper electrode
During the infiltration, viscous Cu liquid flows and fills the pores in, which further improve the densification. When the Co content exceeds 0.2%, the pores in the material substantially eliminated, and a large number of solid phase tungsten particles is connected with each other to form continuous skeleton, which limit the flow of liquid Cu, block the increase of densification, and decrease the density because of the growth of tungsten particle.

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Formation of Heterotypic Substitutional Solid Solutions (NH4)10–xKx[H2W12O42] · n H2O in the Ammonium Paratungstate ‘Z'/Potassium Paratungstate ‘Z' System

Category: Tungsten Information
Published on 08 December 2015
The synthesis of four solid solutions (NH4)10–xKx[H2W12O42] · n H2O (x/n: 6.9/9.7, 5.9/9.5, 3.3/8.5, and 2.6/9.0) with the structure of triclinic K10[H2W12O42] · 10 H2O (I) and two solid solutions (x/n: 3.1/4.0, and 2.6/4.0) with the structure of monoclinic (NH4)10[H2W12O42] · 4 H2O (II), was accomplished by a new method from ammoniacal monotungstate solution by adding the appropriate amount of potassium hydroxide and the release of ammonia during evaporative crystallization. The preparation of corresponding single crystals was achieved by slow evaporation of saturated solutions of the corresponding polycrystalline samples according to the method of isothermal evaporation.
 
The study of coordination and space filling behavior of the potassium and ammonium cations, crystal water molecules, and the paratungstate ‘Z' anion revealed that the predominance of the triclinic structure (2.6 ≤ x ≤ 10.0) in the system is effected by the bulkiness of NH4+. The transition area (2.6 ≤ x ≤ 3.1; 4 ≤ n ≤ 8.5) with coexisting triclinic and monoclinic mixed crystals represents the miscibility gap, typical for a heterotypic substitutional solid solution. The ‘resistance' of three specific K+ positions, to be substituted by NH4+, is caused by peculiarities of bond lengths, coordination numbers, and character of coordinated neighbors.
 
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Ammonium Paratungstate Tetrahydrate and Highly Pure Ammonium Paratungstate Tetrahydrate Method Producing

Category: Tungsten Information
Published on 08 December 2015
The invention is directed to a method for the production of ammonium paratungstate tetrahydrate by thermal treatment of ammonium paratungstate decahydrate in an aqueous suspension. The ammonium paratungstate tetrahydrate can be produced with high purity and high yield. The production method may furthermore be carried out in a simple and energy-efficient manner.
 
The invention is related to a process for preparing ammonium paratungstate tetrahydrate which comprises converting ammonium paratungstate decahydrate suspended in an aqueous phase into ammonium paratungstate tetrahydrate by heating.
 
In the light of this prior art, it is an object of the present invention to provide an economical process which allows a highly pure ammonium paratungstate tetrahydrate to be prepared in a high product yield in a simple process.
 
A further object of the invention is to provide an ammonium paratungstate tetrahydrate having a very high purity.
 
Example 
100 liters of an ammonium- and tungsten-containing solution containing 3.5 g/l of NH3, 45.2 g/l of W and 50 liters of deionized water were placed in a heatable 200 liter stirred reactor. 200 kg of APT decahydrate were added while stirring. The suspension was subsequently treated at 85° C. for three hours while stirring. The NH3 concentration of the liquid phase was 3.5 g/l at an NH3:W molar ratio of 0.83:1. The pH at room temperature was 6.9. The mass ratio of solid to aqueous solution was 1.14:1. After the treatment, the suspension was filtered, the product was washed with 10 liters of deionized water and finally dried at 100° C. The amount of product was 190 kg. This corresponded to a yield of 98.1%.
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Co-doped Effects on Tungsten Copper Electrode III

Category: Tungsten Information
Published on 07 December 2015

Sintering additives, which can dissolve tungsten, can be used for decreasing the porosity of tungsten copper electrode. The most common method is to add active elements, which takes advantage of active elements to dissolve tungsten and improve phase precipitation, round and accumulation, to obtain a high density. It can remarkably improve the properties of tungsten copper, decrease the sintering temperature and shorten the sintering time. The effect of different content of Co element on the hardness of tungsten copper electrode as follow:

tungsten copper electrode















We can learn from the graph that the effect of Co element on the hardness of tungsten copper electrode is similar to the density of tungsten copper electrode, which remarkably increases at the beginning and tends to stabilization or decrease. When the content of cobalt is about 0.3%, the density and hardness of tungsten copper electrode reaches the maximum 16.69g/cm3, and HB311.6.

More infomations about Co-doped effects on tungsten copper electrode, click here:

http://news.chinatungsten.com/en/tungsten-information/81018-ti-10447 
http://news.chinatungsten.com/en/tungsten-information/81083-ti-10458

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Co-doped Effects on Tungsten Copper Electrode II

Category: Tungsten Information
Published on 07 December 2015

Adding activate element to promote tungsten dissolution, and of the solid phase sintering and liquid phase diffusion densification during sintering tungsten particles dissolved in the liquid phase precipitation, round and accumulation, to obtain a high density. Its addition can remarkably improve the material properties, reduce the sintering temperature and shortening the sintering time.

However, the addition of these elements will be activated in a certain extent, reduce the thermal conductivity and electrical conductivity of tungsten copper electrode. Therefore, this kind of method is suitable for the occasions, which has lower demands of thermal conductivity and electrical conductivity. The effect of different content of Co on the density of tungsten copper electrode as follow:

tungsten copper electrode















The graph shows that the reaction of tungsten copper electrode density is sensitive to the adding Co element, which increases at the beginning, 14.9g/cm3 rapidly increases to 16.6g/cm3. Afterwards, the content of Co increases constantly, the density of tungsten copper electrode changes a little and has a decreasing trend.

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Thermal Decomposition of Ammonium Paratungstate Hydrate in Air and Inert Gas Atmospheres

Category: Tungsten Information
Published on 07 December 2015
In this study, the thermal decomposition of ammonium paratungstate hydrate was investigated in dynamic air and inert gas (nitrogen and argon) atmospheres by simultaneous thermo-gravimetric analysis (TGA), differential thermal analysis (DTA) and mass spectroscopy (MS). The intermediate and end products obtained during thermal decomposition of ammonium paratungstate hydrate were characterized by X-ray powder diffraction (XRD) and Fourier transform infrared spectroscopy (FT-IR).
 
It was found that the kind of gas was not effective on the thermal decomposition mechanism of ammonium paratungstate hydrate below 665 K. In the first decomposition step, anhydrous ammonium paratungstate was obtained by dehydration. In the second decomposition step, only deammoniation occurred and ammonium hydrogen tungstate was obtained. During the third decomposition step, dehydration, deammoniation and reduction of some tungsten atoms to lower valences were observed. At this stage, first, ammonium hydrogen tungsten oxide bronze and later ammonium tungsten oxide bronze were formed by two serial reactions. In the fourth step which occurs after 665 K, ammonium tungsten oxide bronze formed stoichiometric tungsten oxide in air atmosphere and tungsten suboxide in inert gas atmosphere.
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