Blast Furnace Slides, IIT Roorkee
Blast Furnace Slides, IIT Roorkee
Blast Furnace Slides, IIT Roorkee
o
250 C
CO+N2
Stack
o
1200 C
Bosh
o
1700 C
Tuyeres
o
1500 C
o
1350 C
Hearth
In the upper part of the
furnace, free moisture is
driven off from the
burden materials and
hydrates and carbonates
are disassociated.
In the lower part of the blast
furnace shaft, indirect
reduction of the iron
oxides by carbon
monoxide and hydrogen
occurs at 700-1,000 C.
In the Bosh area of the
furnace where the
burden starts to soften
and melt, direct reduction
of the iron [and other]
oxides and carbonization
by the coke occurs at
1,000-1,600 C. Molten
iron and slag start to drip
through to the bottom of
the furnace [the hearth].
Modern blast furnace runs continuously day and night for some three to seven years and
thereafter the furnace must be shut down for repairs.
Charge: Lumpy iron ore (10/40mm), in the form of hematite or magnetite or iron oxide in the
form of pellets and sinters, flux and metallurgical coke form the charge to the blast furnace. The
physical nature of the solid material and lateral distribution of the charge are of great
importance- fundamentally the action of the iron blast furnace (or any shaft furnace) involves
the chemical reaction between the solid charge and the rising column the gas in the furnace.
The charge must, therefore, be uniformly porous to permit a uniform flow of gas through the
interstices.
A blast furnace cannot be charged with all the fine material because a good deal of it would be
blown out by the gas current, and part of it would pack in such a way as to cause the gases to
channel and leave portions of the charge cold and un-smelted.
Smelting Action: The iron blast furnace operates on a counter-current principle: the charge
moves slowly down in the furnace shaft and current of gas that reacts with the charge moves
upward. This operation is reduction smelting.
•The impurities (are removed) react with calcium oxide to make a liquid slag that floats on top of the molten
iron. The slag is collected after the denser iron has been run out of a tap hole near the bottom of the furnace.
The production of iron in a Blast Furnace is a continuous process.
•The furnace is heated constantly and is re-charged with raw materials from the top while it is being tapped
from the bottom. Iron making in the furnace usually continues for about ten years before the furnace linings
have to be renewed.
Refining iron
•The metal that leaves the Blast Furnace contains between 4% and 5% of carbon. This much carbon makes a
very hard but brittle metal which is not much use. The next step in the production of steel is to reduce the
levels of carbon and other impurity elements in the hot metal.
Segregation and angle of repose
Coke 35 - 38 deg.
Sinter 29 - 33 deg.
Pellets 25 - 26 deg.
Temperature profile of the
blast furnace
• The performance level of blast furnace has enhanced remarkably during the last 2 decades
leading to higher cost efficiency.
• Presently, a single large size furnace produces more than 10000 tons of hot metal per day
(tpd).
•Notable features of the efficient BF in good International scenarios are:
•Productivity, t/day/cu m .. >2.5, Coke rate, kg/ton of hot metal (thm) <300, Coal rate, kg/ton of
hot metal (thm) ~200, Silicon content, % 0.3, Sulphur content, % 0.020, Utilisation, % .. >98%,
Campaign life, years .. >15
The Blast Furnace as a countercurrent mass and heat exchanger
The driving force i.e., the counter current process creates voidage at the indicated areas
causing the burden to descend
Burden Weight
• Pellet:
• Porous hematite:
Oxide Pure Fe
Blast furnace
Tops
Coke only: Plug flow Coke/ore layers
Upward Force by Liquid in Hearth
Resulting upward force:
6.5 ton/m³
Weight of coke:
1.0 ton/m³
Reduction progress:
quenched furnace
The principal reducing agent is the CO in the gas and
equation (1-4) indicates that iron oxide are reduced by CO.
The coke itself has practically no reducing action in the
upper part of the furnace. At high temperature carbon
oxidises carbon (6) and CO2 can not exist over 10000C in
the presence of free carbon; CO therefore can not act as a
reducing agent in the lower part of the furnace, without
being oxidised to CO2.