| Initial processing of chromite ores can be by hand sorting
of lumpy ores, and by heavy media or gravity separation of finer
ores, to remove gangue or waste materials and produce upgraded
ores or concentrates. Magnetic separation and froth flotation
techniques have also been applied in some cases.
Most of the world's production of chromite (95%) is used in
the metallurgical industry in the form of ferrochromium alloys.
The alloys are produced by high temperature reduction (smelting)
of chromite. They are essentially alloys of iron and chromium
with much lesser amounts of carbon and silicon, the amounts
depending upon the grade or type of alloy, and impurities such
as sulphur, phosphorous and titanium.
The conversion of chromite to ferrochromium alloys is dominated
by electric submerged arc furnace smelting with carbonaceous
reductants, predominantly coke, and fluxes to form the correct
slag composition. The electric current is 3-phase Alternating
Current (AC) and the furnaces have three equally spaced consumable
graphite electrodes in a cylindrical, refractory-lined container
with a bottom tap-hole.
Characteristics of the submerged arc furnace for smelting chromite
include:
- Relatively easy to control provided the charge is well
sorted to maintain a permeable overburden which will allow
easy escape of the gases produced.
- Self-regulating with power input determining the rate of
consumption of charge (overburden)
- Some pre-heating and pre- reduction of the overburden by
the hot ascending gases.
Submerged arc furnaces can be open, semi-closed or closed with
correspondingly better thermal efficiency and the ability to
make use of the energy in the off-gases from the closed furnaces.
In the early days of high-carbon ferrochromium production, the
furnaces were supplied with high-grade, lumpy chromite from
countries such as Zimbabwe but with the increasing demand from
the 1970s, other countries, South Africa in particular, commenced
production from their lower-grade ores. The alloy produced from
these ores became known as charge chrome because the chromium
content was lower and the carbon content, and in particular
the ratio of C:Cr, was very much greater than in high-carbon
ferrochromium. This did not suit the stainless steelmakers who
required as little carbon as possible entering their melts for
each chromium unit and who were, therefore, having to use larger
amounts of the more costly low-carbon ferrochromium to compensate.
However, the situation changed radically with the advent of
the argon-oxygen decarburising (AOD) and vacuum-oxygen decarburising
(VOD) processes. These processes enabled the steelmakers to
remove carbon from the stainless melts without excessive oxidation
and losses of chromium.
A more advanced attempt to overcome the problem of ore fines
was the introduction of DC arc, or plasma, furnace technology.
The DC arc furnace uses a single, central hollow graphite electrode
as the cathode, with an electrically conducting refractory furnace
hearth as the anode. The furnace operates with an open bath,
so there is no problem with overburden, and the chromite fines,
together with coal and fluxes, are fed directly into the bath
through the hollow electrode. The furnace has a closed top.
Some of the advantages of DC arc furnace operation are: use
of fine ores without agglomeration, use of cheaper reductants
and greater choice of reductants, higher chromium recoveries,
deliberate changes in the charge composition are reflected rapidly
in the slag or metal, and closed top operation allows furnace
off-gas energy to be used.
Another approach to friable ores has been to pelletise them,
after further grinding if necessary, with binder, reductant
and fluxes and pass them through a rotary kiln where they are
hardened (sintered), pre-heated and pre-reduced to a degree
before charging to a submerged arc furnace.
A further development in treating ore fines by kiln pre-reduction
used unaglomerated chromite fines and low cost coal, with fluxes,
as the feed to the kiln. Self agglomeration of the fines was
achieved close to the discharge from the kiln where the charge
becomes pasty in a high temperature zone of approx. 1,500ºC.
Very high degrees of reduction were achieved (80-90%) so that
the downstream electric furnace (DC arc) became essentially
a melting furnace.
A more recent approach, and one which is being installed by
more plants, is again by pelletising. Pellets are produced with
coke included and these are sintered and partly pre-reduced
on a steel belt sintering system. From there, the pellets are
delivered to pre-heating shaft kilns that are sited above submerged
arc furnaces and which operate as direct feed bins, making use
of the off-gas heat from the furnaces. Lump ore, coke and fluxes
are also directed to the feed bins.
In addition to the technologies already discussed, there have
been various other approaches to smelting chromite. These include
rotary hearth sintering and pre-reduction of pellets, and fluidised
bed pre-heaters for chromite fines.
Some intensive development work has been carried out in Japan
upon entirely coal/oxygen based smelting processes using no
electrical energy, sometimes referred to as smelt-reduction
processes. 
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