Uses of Titanium Dioxide
Uses of Titanium Dioxide
Uses of Titanium Dioxide
Table 1 Comparison of the two processes for the manufacture of titanium dioxide.
Before the titanium dioxide is extracted, the iron ions must be removed from the solution
so that the colour of the final product is not spoiled. The solution is therefore reacted with
recycled iron sources to convert any iron(lll) ions that may be present to iron(ll) ions:
The solution is allowed to stand so that the unreacted solid settles, and the clear liquid is
poured off before being concentrated by evaporation. Cooling then allows light green
crystals of iron(ll) sulfate to form and to be filtered off. These are sold separately. The
remaining solution contains titanyl sulfate, TiOSO 4
Heating evaporates the water and decomposes any remaining sulfuric acid in the solid.
After cooling, the product is 'milled' to form crystals of the size needed. Crystals may
also be coated with another substance, such as aluminium oxide or silica, to make the
titanium dioxide mix more easily with liquids or to make the water-based paints made
from it last longer.
This coating is achieved by dispersing the dry product from the calciner in water
containing the dissolved coating chemicals which precipitate from solution onto the
TiO2 crystals. The coating is usually between 3 and 8% by weight in the final dried
pigment. This coating is achieved by changing the temperature and pH of the solution.
Each TiO2 crystal needs to be coated uniformly to maximize the effectiveness of the
coating. The coated TiO2 crystals are filtered from the water and dried before being
packed for dispatch to the final customer.
Feedstock containing, titanium dioxide (85% pure) and finely divided coke are
added to chlorine gas in a reactor, where the titanium dioxide undergoes
chlorination reaction at 800 ºC.
The rutile is fed into a heated bed together with a source of carbon, usually coke.
Chlorine is fed into the bed and the reaction takes place to form titanium (IV) chloride in
the vapour form which is removed from the bed. Iron and other metals in the ore are
chlorinated and also leave the bed in the vapour state. The oxygen in the ores is
combined with the carbon to form carbon monoxide and dioxide.
Pressure is maintained at about 1.5 atm and the residence time in the reactor is about 1
hour. The outlet stream from the chlorinator at 800°C is fed to a cooler and cooled to
320°C using water as coolant. Iron chloride condenses and settles down as liquid.
Unreacted solids also settle down and are separated. The vapor stream from the top is
fed to the condenser.
The gas stream from the cooler is cooled to 137ºC where TiCl 4 is condensed. The
effluent gas is then sent to a converter, where Carbon monoxide is converted into Carbon
dioxide. The condensed pure TiCl4 liquid at its bubble point is fed to the oxide burner.
Pure TiCl4 liquid is vaporized and burnt with oxygen to form titanium dioxide solid (0.3μm
particle size) and chlorine gas. The reaction takes place at a temperature of 1000ºC.
The stream containing chlorine gas and titanium dioxide solids are separated using a
high efficiency Cyclone Separator. The Chlorine gas is recycled to the Chlorinator. The
product is removed, cooled and surface treated
(The vapour stream is cooled and the metal chlorides other than titanium (IV) chloride are
condensed and solidified. The titanium (IV) chloride vapour, which contains almost pure
titanium (IV) chloride and has a lower boiling point, is then condensed and stored as
liquid. It is then reboiled and distilled to give a purer product to feed to the next stage.)
The titanium dioxide is formed (by adding seed crystals) as a fine solid in the gas stream
and is filtered out of the waste gases using cyclones or filters. Once again control of
crystal growth is important to give particles of the correct size for pigments. This is done
by adding nucleating agents to the gas stream (e.g. water or aluminium chloride) and by
cooling the products. The chlorine in titanium(IV) chloride is released and recycled to the
chlorination stage of the process above.
The product contains small amounts of absorbed chlorine gas which are removed.