How to make Tungsten Carbide Tools
Tungsten
carbide, often simply “carbide,” is a familiar material around the industry.
This compound of tungsten and carbon has revolutionized the metal-cutting world
over the decades, enabling increased speeds and feeds and providing longer tool
life.
It was first
theorized as a tool for cutting material in 1925, by Dr. Samuel Hoyt, a scientist
of the Research Laboratory of the General
Electric Company at Schenectady. He also developed Carboloy, an
alloy of tungsten, carbide, and cobalt which later GEC opened as the Carboloy
division to produce tungsten carbide cutting tools. In the late 1930s, Philip
M. McKenna, founder of Kennametal, found out that by adding a titanium compound
to the mix, it made the tools work better at higher speeds. This began the forward
march toward today’s lightning-fast cutting speeds.
Tungsten carbide (WC) is an inorganic non-natural compound composed of
equal parts of tungsten (W) and carbon (C) atoms. Tungsten Carbide exhibits
a hexagonal structure lattice made of a grid of those tungsten
and carbon. It’s most striking properties, that make it useful for making
tools, are a high density, a very high melting point of 2600 °C. It is
also a very hard compound and also has the metal-like, high values of
electric and thermal conductivity. Tungsten carbide is approximately twice
as strong as steel.
Prior
to 1945, tungsten carbide was prepared by melting tungsten, carbon black and
metal oxides at a temperature of 2000 °C but the tools made from this metal
were found to be far too brittle for industrial use.
Making of Tungsten Carbide Tools
Mining & Processing
There are
several tungsten ores that can be mined and refined into tungsten or made into
tungsten carbide. Wolframite is the best known. Scheelite and/or wolframite are commonly located in narrow
veins which are very slightly inclined and often widen with the depth.
The ore is then crushed,
heated and treated with chemicals. The result: tungsten oxide. Then, the fine
particles of tungsten oxide are carburized, turning them into tungsten carbide.
In one method, the tungsten oxide is mixed with graphite (carbon). This mixture
is then processed continuously and heated to over 1200˚ C (2200˚ F) which
causes a chemical reaction that removes the oxygen from the oxide and combines
the carbon with the tungsten to yield tungsten carbide.
Grain
Size and Grading
Once processing is
done, the carbide grain sizes will determine the mechanical properties of the
final product. This is key in its processing. The size of the tungsten oxide
particles, and how long and at the temperature that the oxide/carbon mixture
may have been processed decided or as such creates the size of the carbide
grain.
So, as consequences go, if the size of the
grain is too large and the percentage of binder used is much higher in
comparison, the carbide deforms under this pressure. Now, one of the major
advantages of carbide to be alloyed with tungsten is its proficiency to cope
under pressure or compressive force. If the alloy now is too soft it loses that
ability.
The tungsten carbide
particles processed are received at a fraction of the size of a grain of sand.
A series of sieves are used to sort out the different grain sizes: less than
one micron, one and one half microns, and so forth.
Now, the tungsten
carbide grains, after sieving, are ready for blending into “grade powder.” In
the tungsten carbide industry, one speaks of grades rather than alloys, but
they mean the same thing.
The story of Tungsten Carbide (WC) and its powder metallurgy,
and particularly that of the hard metal industry, is depicted by a
progressively widening range of available grain sizes; whilst simultaneously
narrowing the grain size distribution for each grade of WC powder.
The tungsten carbide
grains go into a mixing vessel with the other components of the grade. Powdered
cobalt metal is made to act as the “glue” to hold all the components. The other
materials, such as titanium carbide, tantalum carbide and niobium carbide are
added to improve the properties of the material when cutting.
Pressing
Once the mixing process
is completed, the liquid must now be removed. This generally happens in a spray
dryer, that looks similar to a stainless steel silo. An inert, drying gas, one
of nitrogen or argon, is blown into the spray dryer from the bottom up. Once all
the liquid is removed, the sand like remaining dry material is the “grade
powder”
The grade powder then goes
into insert shaped molds that are specially designed and made to allow for the
shrinkage that will happen later on in the process to create the cutter inserts.
Just as pharmaceutical tablets are formed, in a process similar to that, the
powder is compressed into the molds.
Heating
After pressing is
completed, it is fairly delicate and the form looks like oversized inserts.
These inserts are then removed from the like-shaped molds and are placed on
graphite or molybdenum trays, and go into a sintering furnace where they are
heated in a low-pressure hydrogen atmosphere to 1100-1300˚ C (about 2000- 2400˚
F). Any cobalt present melts. The insert in the furnace consolidates into a
solid, smaller size.
The inserts are removed
from the furnace and are now cooled. On cooling, they become dense and hard. A
quality control check is performed. The inserts, after the check, are usually
ground or honed to achieve the correct dimensions and cutting edge. Honing, done
to a radius of 0.001″ is typical, though some of these parts receive a
cutting-edge radius of half a thousandth or as large as 0.002″, and some of
these are left extremely sharpened as sintered in the furnace.
The next step is
grinding and other such operations. Even still, some of the types and designs
of inserts retrieved from the sintering furnace are in their final shape and
have the correct edge as well. Hence, they do not need further grinding.
Introducing Tungsten
Tungsten
occurs naturally in nature as Wolframite, FeMnW04, and Scheelite, Ca W04.
The
ore is digested in hydrochloric acid to remove the calcium and to precipitate
tungstic acid, H2W04, which is then dissolved in ammonia
and crystallized as ammonium tungstate, (NH4)2W04.
Ammonium tungstate is evaporated by boiling to give ammonium paratungstate, or
APT, 5(NH4)2O.12W03.5H20. At
temperatures below 500C, fine APT is obtained. By calcining APT or
tungstic acid, tungsten oxide, W03, is obtained. The lower the
temperature, finer the W03 produced. When W03 is reduced
in hydrogen, tungsten, W, is produced: because oxygen forms a more stable.
Coating
Cutting conditions may
not be optimal and hence the tools’ lives need to be prolonged so as to face
these conditions. Many types and combinations of coatings have been developed.
They can be applied in two ways: by chemical vapor deposition (CVD) or physical
vapor deposition (PVD). Both types are applied in furnaces.
Chemical vapor deposition
For CVD, the coating is
usually 5- 20 microns thick. Milling and drilling inserts usually receive
5–8 icrons, as these operations require better surface finish, and they
encounter more impact, so they require greater edge toughness. For turning
applications, the coatings tend to be in the range of 8–20 microns. In turning,
heat and abrasion tend to be more of a concern.
In its simplest explanation, CVD involves flowing a
precursor gas or gases into a chamber containing one or more heated objects to
be coated. Chemical reactions occur on and near the hot surfaces, resulting
in the deposition of a thin film on the surface.
Physical vapor deposition
PVD coatings are
typically about 2-4 microns thick. Different manufacturers use different
numbers of layers. These PVD coatings are well-suited to applications cutting
high temperature, nickel-based, cobalt-based or titanium-based materials, and
sometimes steel and stainless steel.
Tool manufacturers are
meeting the pressures for ever increasing feeds and speeds, and the need for
longer tool life and lower costs, by continually improving the designs of
tungsten carbide cutting tools and developing better and better coating
technologies.
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