Tiwest JV
Tiwest JV mines and processing plants: The Tiwest JV mines and processing plants operate in an
integrated manner such that ilmenite originating from the mines is processed through to the finished product
of titanium dioxide pigment.
HMC is produced at the primary concentrating plants (“PCP”) at Cooljarloo then transported to Chandala.
Mineral products are produced in the MSP at Chandala. Ilmenite from the MSP is taken directly into the
adjacent synthetic rutile plant (“SRP”). Synthetic rutile either is transported to the pigment plant at Kwinana
or exported. Waste products from the processing plants at Chandala and Kwinana are returned to Cooljarloo
for final disposal.
Separate PCPs operate in the two mining areas at Cooljarloo. In the Cooljarloo South mine two dredges mine
in parallel to feed the PCP at 2,200tph, which floats in the dredge pond. In the Cooljarloo North mine scrapers
dump ore into a slurrying hopper to feed the land-based PCP at 650tph. This PCP can be relocated when the
mine advances beyond an economic pumping distance. The PCPs have similar flowsheets.
Gravel, rock and clay lumps are removed from the slurried ore by a rotating trommel. The resulting sand slurry
is deslimed by hydrocyclones before treatment in a conventional spiral circuit. HMC containing approximately
96% heavy minerals is stockpiled by hydrocyclone. Sand tailing is pumped back to the mined out area to
reform the land surface. Slime tailing from the North mine, derived from higher slime containing ore, is thickened before pumping to shallow solar drying areas. Slime tailing from the South mine settles in the
dredge pond from where it can also be pumped to solar drying areas when required. The combined output of
concentrate from the two PCPs is up to 800,000tpa. The two concentrates are blended before trucking to
Chandala.
The maximum treatment rate of HMC at the MSP is 90tph. The total consumption is 740ktpa leaving the
possibility of stockpile accumulation at the mines. The flowsheet required to separate mineral products in the
MSP is complex. The HMC is first attritioned to remove coatings from the mineral grains and screened to
remove coarse oversize grains. The resulting concentrate is dried and heated before electrostatic separation
to separate the conducting minerals ilmenite, rutile and leucoxene from the non-conducting mineral zircon and
most of the trash minerals including quartz, monazite and kyanite. Ilmenite, rutile and leucoxene are
separated into products by magnetic separators. The non-conducting minerals are classified into two size
ranges and magnetically cleaned before reslurrying then concentrating on wet tables, spirals and Kelsey jigs.
The concentrates are dried then zircon is produced after many stages of electrostatic and magnetic
separation. A small output of staurolite, derived from the coarse non-conductor magnetics, has recently been
added to the products.
The Becher Process employed in the Chandala SRP is an elegant combination of pyro and hydrometallurgy
which removes most of the iron oxide portion of ilmenite and about 50% of the manganese oxide impurity
resulting in synthetic rutile containing up to 93% TiO2.
Ilmenite and Collie sub-bituminous coal are mixed in a rotary kiln. The coal is combusted to provide carbon
monoxide for reduction and heat up to 1,100ºC. Iron oxide is reduced to metallic iron within the ilmenite grains.
Sulphur is also introduced to the kiln to sulphidise manganese oxide within the grains. The reduced ilmenite
is cooled and separated from coal char, which is recycled to the kiln.
Excess char is cleaned for sale as activated carbon. The reduced ilmenite is then slurried in aeration tanks
with a weak solution of the oxidising catalyst ammonium chloride. Each batch is sparged with air while being
agitated until the metallic iron has been reoxidised. During this process iron migrates from the reduced
ilmenite to form separate particles of iron oxide less than 5 microns in diameter. Iron oxide is separated from
synthetic rutile by hydrocyclones. The synthetic rutile is then agitated with dilute sulphuric acid to remove
manganese sulphide and residual iron.
Treatment and disposal of waste products is a major part of the process, which occurs in the waste
management plant. Iron oxide slurry is thickened and filtered. Acidic effluent is neutralised and the
precipitates thickened and filtered. Sulphurous liquor from the kiln waste gas scrubber is treated with a double
alkali process and the precipitates thickened and filtered. All liquors are recycled to the SRP. All filter cakes
are returned to the mine for disposal.
The capacity of the SRP has been gradually increased to 220ktpa. An increase to 240ktpa is currently
underway and is forecast to produce at that rate in 2006. Ilmenite consumption will rise to a maximum of
400ktpa, which still allows excess ilmenite from the MSP to be stockpiled at Chandala. This stockpiled
ilmenite of high quality has the potential to maximise kiln capacity in the future if blended with lower quality
ilmenite from orebodies developed to replace Cooljarloo North.
Kwinana Pigment Plant: The plant is situated in Kwinana, Western Australia where the process employed is
the Chloride Process. The technology is provided by the Tronox Inc of Oklahoma. The initial capacity of the
plant was 54.6ktpa when the plant was commissioned in 1991. The plant has since been expanded, largely
by de-bottlenecking, to the point where the capacity is now 108,000tpa.
The feedstock for the plant is synthetic rutile (“SR”) which is obtained from the Tiwest JV synthetic rutile
production plant located near Muchea about 70km north of Perth. The feedstock has a TiO2 grade of around
93%. The TiO2 part of the synthetic rutile comprises mainly iron oxide as well as other metal oxides. The
impurity – TiO2 metal oxides – must be separated from the TiO2 because, in general, these TiO2 metals impart
colour to pigment other than the desired white colour. The separation of the TiCl4 from the other metal
chlorides is achieved as described below.
Firstly almost all the SR is converted to a metal chloride vapour. Titanium tetrachloride (“TiCl4”) is one of the
most volatile of the metal chlorides and has the convenient property that TiCl4 is a liquid at ambient
temperature and pressure. The SR is reacted with chlorine and coke to produce a mixture of metal chloride
vapour (mainly TiCl4), carbon monoxide, carbon dioxide and a small amount of hydrochloric acid vapour. This
reaction is carried out in a fluid bed reactor referred to as a chlorinator. On leaving the chlorinator the exit gas
is cooled. As the exit gas cools most of the metal chlorides other than TiCl4 freeze out as solids.These solids
are separated in a waste solids cyclone and are quenched with water to form an acidic metal chloride solution
which is then transferred to the Effluent Treatment Plant. The gas passing through the waste solids cyclone now contains TiCl4 vapour, carbon monoxide, carbon dioxide and a small amount of hydrochloric acid vapour.
The gas is further cooled to condense out the TiCl4 as a liquid. This TiCl4 liquid is then treated and distilled
to produce a pure form of TiCl4. This purified TiCl4 is stored prior to being used as the feedstock for the
Oxidation Plant. The non-condensable gases report to the Waste Gas Scrubbing train. Waste gas is scrubbed
with water to remove the hydrochloric acid vapour and forms a saleable 28% Hydrochloric Acid product.
TiCl4 can be burned with oxygen in a special burner (called an Oxidizer) to form rutile (one of the crystal forms
of TiO2) crystal particles in a size range where they exhibit maximum light scattering properties. Light
scattering translates to hiding power, which is the chief commercial property of TiO2 pigment. In order to
stabilise the rutile crystal it is doped with a small amount of aluminium, which is achieved by dissolving a small
amount of aluminium chloride in TiCl4 prior to oxidation. Gaseous oxygen is obtained from the L’Air Liquide
plant in Kwinana by pipeline.
During the oxidation process chlorine is liberated from the TiCl4. This chlorine is separated from the TiO2
product and is recycled to the Chlorination Plant. The TiO2 product from the Oxidation Plant is referred to as
Raw Pigment. Raw Pigment particles do not mix into paint resins very well. To facilitate the incorporation of
Raw Pigment into resins an alumina coating is applied to the Raw Pigment particles. Some grades of pigment
will also be coated with silica and zirconia to enhance the durability of the paint. These coating steps are
carried out in the Pigment Finishing Area. The main reagents consumed in the process to carry out these
coatings include Sodium Aluminate, Sodium Silicate, Zirconium Oxychloride, Caustic Soda and Sulphuric Acid.
Raw Pigment slurry is first subjected to Sand Milling to breakup agglomerates of pigment. The product from
the Sand Milling section is then cycloned and screened to remove remaining oversize particles. The screened
Raw Pigment slurry is then fed to the Treatment Tanks where the coatings are applied. The product slurry
from the treatment section is washed on rotary vacuum filters to remove remaining soluble chemical from the
treatment process. The washed pigment slurry is then fed to gas-fired Dryers which remove water from the
pigment. The pigment is then micronised. Micronisation is a process whereby pigment agglomerates are
broken into particles of only a few microns in size. This is accomplished using high pressure steam jets in a
device known as a microniser. The micronised pigment is then cooled and bagged into 25kg paper bags or
bulker bags. The major part of the pigment produced goes into paper bags. The paper bags are shipped on
pallets which are shrink-wrapped for protection against moisture.
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