Title of Invention

A DIRECT REDUCTION PROCESS

Abstract A direct reduction process for a solid metalliferous material having a particle size distribution that at least in part comprises micron sized particles, comprises supplying the metalliferous material, a solid carbonaceous material, an oxygen-containing gas, and a fluidizing gas into a fluidized bed in a vessel and maintaining the fluidized bed in the vessel, at least partially reducing metalliferous material in the vessel, and discharging a product stream that comprises the at least partially reduced metalliferous material from the vessel. The process is characterized by: (a) establishing and maintaining a carbon-rich zone within the fluidized bed; (b) passing metalliferous material, including metallised material (which term includes partially metallised material), through the carbon-rich zone; and (c) injecting the oxygen-containing gas into the carbon-rich zone and oxidizing metallised material, solid carbonaceous material and other oxidisable solids and gases and causing controlled agglomeration of particles.
Full Text The present invention relates to a direct reduction process for a metalliferous feed ma-
terial, particularly, although by no means exclusively, to a direct reduction process for
an iron-containing feed material, such as iron ore.
The present invention also relates to a process for reducing a metalliferous feed mate-
rial that comprises a direct reduction process for partially reducing metalliferous feed
material in the solid state and a smelting process for melting and further reducing the
partially reduced metalliferous feed material to a molten metal.
The present invention was made during the course of an on-going research project car-
ried out by the applicant to develop the so called "CIRCOFER technology" for the direct
reduction of iron ore.
CIRCOFER technology is a direct reduction process that is capable of reducing iron ore
in the solid state to a metallisation of 50% or higher.
CIRCOFER technology is based on the use of fluidised beds. The main feed materials
to the fluidised beds are fluidising gas, metal oxides (typically iron ore fines), solid car-
bonaceous material (typically coal) and oxygen-containing gas (typically oxygen gas).
The main product produced in the fluidised beds is metallised metal oxides, i.e. metal
oxides that have been at least partially reduced.
One of the findings of the applicant in the research project is that it is possible to oper-
ate the process with relatively fine feed materials and minimise carry-over of iron units
in an off-gas stream from the process and minimise undesirable accretions of materials,
such as metal oxide fines, on exposed surfaces in the fluidised bed apparatus that are
capable of disrupting the process. High carry-over of iron units in off-gas streams and
undesirable accretions on exposed apparatus surfaces are significant issues for com-

mercialisation of the CIRCOFER technology, particularly with metal oxide feed materi-
als that are relatively brittle.
The applicant has found that it is possible to achieve controlled agglomeration of parti-
cles and minimise undesirable accretions of materials, such as metal oxides, by provid-
ing a carbon-rich zone in a fluidised bed, passing metalliferous material through the
zone, and injecting oxygen into the zone and oxidising smaller particles, including
smaller metallised particles.
According to the present invention there is provided a circulating fluidized bed process for
direct reduction of a solid metalliferous material having a particle size distribution that at least
in part comprises micron sized particles, said process comprising: supplying the metalliferous
material, a solid carbonaceous material, an oxygen-rich gas and a fluidizing gas to a vessel,
whereby a fluidized bed is maintained in the vessel, the fluidized bed containing a carbon-rich
zone, withdrawing gas and entrained solids from an upper section of the vessel, separating
solids from the withdrawn gas, and recirculating the separated solids to the vessel, and
discharging a product stream from a lower section of the vessel,
wherein the step of supplying the oxygen-rich gas comprises injecting the oxygen-rich
gas downwardly into the carbon-rich zone using a cooled lance spaced horizontally inward
from side walls of the vessel, whereby heat is generated in the carbon-rich zone by reactions
between oxygen and metallized material, the solid carbonaceous material and other oxidizable
solids and gases in the fluidized bed, metalliferous material is at least partially reduced in a
metal-rich zone below the carbon-rich zone, and the product stream discharged from the vessel
comprises the at least partially reduced metalliferous material, and
wherein the process involves controlling agglomeration of particles by adjusting at least
one of feed rate of the metalliferous material, feed rate of the carbonaceous material and feed
rate of the oxygen-rich gas.
The term "carbon-rich" zone is understood herein to mean a region in the fluidised bed
in which there is a relatively large amount of carbon-containing material in relation to
the amount of metalliferous material than there is in other regions of the fluidised bed.
The applicant does not have a totally clear understanding at this stage of the mecha-
nism or mechanisms that enables controlled agglomeration of metalliferous material to
be achieved. Nevertheless, without wishing to be bound by the following comments, in
the research project the applicant observed that the agglomerates that formed com-
prise smaller particles, particularly fines, adhered to each other and to larger particles.
The applicant speculates that the conditions in the carbon-rich zone, and more particu-

tarty a hot zone within the carbon-rich zone, are such that (a) micron sized partially and
completely reduced, i.e. metallised, iron ore particles react with oxygen and generate
heat and the resultant oxidised particles become sticky (b) fine coal particles react with
oxygen and oxidise and the resultant ash becomes sticky; and (c) fine iron ore particles
become sticky as a consequence of being heated. The applicant also speculates that
these smaller sticky particles, adhere to larger particles that have a higher heat sink
capacity, with the overall beneficial result that there is a reduction in the proportion of
smaller particles in the vessel that can adhere to apparatus surfaces and be carried out
from the vessel in an off-gas stream.
Preferably the process comprises supplying the metalliferous material in the form of
fines.
In the case of reducing metalliferous material in the form of iron ore fines, preferably
the fines are sized at minus 6 mm.
Preferably the fines have an average particle size in the range of 0.1 to 0.8 mm.
One of the advantages of the process is that it can accept a substantial amount of met-
alliferous feed material with a grain size of less than 100 microns without a significant
amount of this material exiting the process entrained in off-gas. This is believed to be
due to an agglomeration mechanism operating within the fluidised bed that promotes a
desirable level of agglomeration between particles of feed materials, particularly sub-
100 micron particles, without appearing to promote uncontrolled agglomeration capable
of interrupting operation of the fluidised bed. Similarly, friable ores that have a ten-
dency to break down during processing and to thereby increase the proportion of parti-
cles in the fluidised bed with a size of less than 100 microns may be processed without
significant loss of feed material in process off-gas.
Preferably the process comprises supplying the metalliferous material with a selected
maximum particle size and controlling agglomeration so that 90% of the particles di-
scharged from the process as a product stream do not exceed the maximum selected
feed size.

Preferably the process comprises supplying the metalliferous material with a selected
maximum particle size and controlling agglomeration so that no more than 30%, prefe-
rably no more than 20%, and more preferably no more than 10% by weight of the total
weight of iron units discharged from the process is carried off in an off-gas stream from
the process.
Preferably the process comprises controlling agglomeration by adjusting the feed rates
of any one or more of the metalliferous material, the carbonaceous material, the reacti-
on temperature and the oxygen-containing gas.
More preferably the process comprises controlling agglomeration by adjusting the feed
rate of the carbonaceous material.
The process has considerable advantages.
By way of example, it has hitherto been thought that CIRCOFER technology requires
amounts of carbon that are at least 20-30% by weight of the total weight of solids in a
fluidized bed to prevent uncontrolled agglomeration leading to undesirable accretions
on exposed surfaces of fluidized bed apparatus that disrupts the process.
The applicant has found that it is possible to operate the process with minimal undesir-
able accretions and with desirable controlled agglomeration with relatively low levels,
typically 5-30%, of carbonaceous material. Low levels of carbonaceous material
means that it is possible to produce a solids product stream with low levels of char and
the product stream can be supplied into smelters with minimal downstream processing.
In addition, controlled agglomeration of metalliferous material fines into larger particles
that become part of the solid products stream rather than being carried out of the proc-
ess as entrained solids in an off-gas stream means that there is higher recovery from
the process and less downstream treatment of off-gas required. This is a particularly
important benefit for iron ores that tend to be brittle and would break down into micron
sized particles in the course of materials handling prior to being supplied to the vessel

and during the course of being processed in the vessel. Such brittle ores include ores
mined in Western Australia, such as Brockman and Mara Maba ores.
On current indications, typically the process can reduce minus 3mm iron ore fines with
the following results.
At least 90% by weight of the iron ore fines supplied to the process being metallised to
some extent and discharged as part of a solids product stream, with less than 50% of
the fines being greater than 2mm.
In the range of 5-30% by weight of the solids product stream comprising carbon.
Less than 20% by weight of the iron ore fines supplied to the process being discharged
from the process with off-gas.
Preferably the process comprises injecting the oxygen-containing gas into a central
region of the vessel, ie a region that is located inwardly of a side wall of the vessel.
Preferably the process comprises injecting the oxygen-containing gas so that there is a
downward flow of the gas in the vessel.
Preferably the process comprises injecting the oxygen-containing gas with a downward
flow in a range of plus or minus 40 degrees to the vertical.
More preferably the process comprises injecting the oxygen with a downward flow in a
range of plus or minus 15 degrees to the vertical.
Preferably the process comprises injecting the oxygen-containing gas via at least one
lance having a lance tip with an outlet positioned in the vessel inwardly of the side wall
of the vessel in the central region of the vessel.
Preferably the lance tip is directed downwardly.
More preferably the lance tip is directed vertically downwardly.

The position of the lance and, more particularly, the height of the outlet of the lance tip,
is determined by reference to factors, such as the oxygen-containing gas injection velo-
city, the vessel pressure, the selection and amounts of the other feed materials to the
vessel, and the fluidised bed density.
Preferably the process comprises water-cooling the lance tip to minimise the possibility
of accretions forming on the lance tip that could block the injection of the oxygen-
containing gas.
Preferably the process comprises water cooling an outer surface of the lance.
Preferably the process comprises injecting the oxygen-containing gas through a central
pipe of the lance.
Preferably the process comprises injecting the oxygen-containing gas with sufficient
velocity to form a substantially solids-free zone in the region of the outlet of the lance
tip to minimise the formation of accretions that could block the injection of the oxygen-
containing gas.
Preferably the oxygen is injected with a velocity in the range 50-300 m/s.
Preferably the process comprises injecting nitrogen and/or steam and/or other suitable
shrouding gas and shrouding the region of the outlet of the lance tip to minimise oxida-
tion of metal that could result in accretions forming on the lance tip that could block the
injection of the oxygen-containing gas.
Preferably the process comprises injecting the shrouding gas into the vessel at a velo-
city that is at least 60% of the velocity of the oxygen-containing gas.
In one embodiment the process comprises establishing reaction zones in a fluidised
bed and moving solids (including metalliferous and carbonaceous materials) and fluidis-
ing gas within the bed so that the solids pass through the reaction zones.

The reaction zones may be contiguous.
One reaction zone is the carbon-rich zone described above.
The other reaction zone is a metal-rich zone in which metalliferous material, such as
iron ore, is reduced in a solid state.
The term "metal-rich" zone is understood herein to mean a region in the fluidised bed in
which there is a relatively large amount of metalliferous material in relation to the
amount of carbon-containing material than there is in other regions of the fluidised bed.
The metal-rich zone is located in a lower section of the fluidised bed and the carbon-
rich zone is located above the metal-rich zone.
The zones may be contiguous.
The fluidised bed comprises upward and downward movement of solids through the
zones.
Preferably the process comprises supplying the metalliferous material, the carbonace-
ous material, the oxygen-containing gas, and the fluidising gas to the fluidised bed and
maintaining the fluidised bed with (a) a downward flow of the oxygen-containing gas,
(b) an upward flow of solids and fluidising gas countercurrent to the downward flow of
the oxygen-containing gas, and (c) a downward flow of solids outwardly of the upward
flow of solids and fluidising gas.
In the fluidised bed described in the preceding paragraph, solids in the upward and
downward flows of solids are heated by heat generated by reactions between the oxy-
gen-containing gas, the carbonaceous material and other oxidisable materials (such as
CO, volatiles, and H2) in the carbon-rich zone. The solids in the downward flow of so-
lids transfer heat to the metal-rich zone.

In addition, the upward and downward flows of solids shield the side wall of the vessel
from radiant heat generated by reactions between the oxygen-containing gas and the
solid carbonaceous material and other oxidisable solids and gases in the fluidised bed.
Preferably the carbonaceous material is coal. In such a situation, the process devolati-
lises the coal to char and at least part of the char reacts with oxygen and forms CO in
the fluidised bed. Coal volatiles also decompose to gases such as CO and H2, which in
turn may further react with oxygen in the fluidised bed.
Preferably the fluidising gas comprises a reducing gas, such as CO and H2.
Preferably the process comprises selecting the amount of H2 in the fluidising gas to be
at least 15% by volume of the total volume of CO and H2 in the gas.
Preferably the process comprises discharging the product stream comprising at least
partially reduced metalliferous material from the lower section of the vessel.
Preferably the product stream also comprises other solids (for example char).
Preferably the process comprises separating at least a portion of the other solids from
the product stream.
Preferably the process comprises returning at least a portion of the other solids to the
vessel.
Preferably the process comprises discharging an off-gas stream containing entrained
solids from an upper section of the vessel.
Preferably the process comprises separating at least a portion of the entrained solids
from the off-gas stream.

Preferably the process comprises maintaining a circulating fluidised bed by separating
entrained solids from the off-gas stream and returning at least a portion of the separa-
ted solids to the vessel.
Preferably the process comprises returning solids separated from the off-gas to the
lower section of the fluidised bed.
Preferably the process comprises preheating metalliferous feed material with the off-
gas from the vessel.
Preferably the process comprises treating the off-gas after the preheating step and re-
turning at least a portion of the treated off-gas to the vessel as the fluidising gas.
Preferably the off-gas treatment comprises one or more of (a) solids removal, (b) coo-
ling, (c) H2O removal; (d) CO2 removal, (e) compression, and (f) reheating.
Preferably the off-gas treatment comprises returning solids to vessel.
The process may be operated to produce a product stream ranging from low to high
metallisation depending on the downstream requirements for the at least partially redu-
ced metalliferous material. The metallisation may range from 30 to In excess of 80%.
In situations in which metallisation greater than 50% is required, preferably the process
comprises operating with reducing gas in the fluidising gas. One option for the fluidi-
sing gas in this instance is treated off-gas from the vessel. In situations in which metal-
lisation less than 50% is required, it is envisaged that it will not be necessary to operate
with reducing gas in the fluidising gas and sufficient reductant can be obtained via solid
carbonaceous material supplied to the process.
The oxygen-containing gas may be any suitable gas.
Preferably the oxygen-containing gas comprises at least 90% by volume oxygen.

The present invention is described further with reference to the accompany drawing
which is a diagram of an apparatus for direct reduction of a metalliferous material by
one embodiment of a process in accordance with the present invention which illustrates
the reaction zones formed by the process within the vessel shown in the Figure.
The following description is in the context of direct reduction of metalliferous material in
the form of iron ore in the solid state. The present invention is not so limited and ex-
tends to direct reduction of other iron-containing materials (such as ilmenite) and more
generally to other metalliferous materials.
The following description is also in the context of direct reduction of iron ore with coal
as a solid carbonaceous material, oxygen as an oxygen-containing gas, and recycled
off-gas containing a mixture of CO and H2 as a fluidising gas. The present invention is
not so limited and extends to the use of any other suitable solid carbonaceous material,
oxygen-containing gas, and fluidising gas.
With reference to the Figure, solid feed materials, namely iron ore (typically fines sized
to less than 6 mm) and coal, oxygen and fluidising gas are supplied to the vessel 3
shown in the Figure and establish a fluidised bed in the vessel.
The solid feed materials are supplied to the vessel via a solids delivery device such as
a screw feed or a solids injection lance 5 that extends through a side wall 7 of the ves-
sel.
The oxygen is injected into the vessel via a lance 9 that has a lance tip 11 with an out-
let that directs the oxygen downwardly in a central region of the vessel, ie spaced in-
wardly from the side wall 7 of the vessel. The lance tip is directed downward in the
vessel. The fluidising gas is injected via a series of tuyeres or nozzles (not shown) in a
base 13 of the vessel.
The above-described supply of solids and gases produces the following reactions in the
vessel.

Devolatilisation of coal fines to char and decomposition of coal volatiles to gaseous
products (such as CO and H2) and reaction of at least part of the char with oxygen to
form CO.
Direct reduction of iron ore to at least partially reduced iron by the CO, H2, which reac-
tions produce CO2 and H2O.
Reaction of CO2 with carbon to form CO (Boudouard reaction).
Oxidation of solids and gases, such as partially reduced iron ore particles, char, coal
volatiles, CO, and H2 (injected as a part of the fluidising gas or produced through de-
composition of coal volatiles) with oxygen which generates heat that assists with main-
taining the reactions described in the preceding dot points and which also contributes
to a desirable controlled agglomeration of the smaller reduced ore particles to form lar-
ger reduced ore particles.
The relative densities of the solids and the above-described injection of the solids and
the gases, including the locations of the solids/gas injection, results in the formation of
reaction zones in the vessel. The zones may be contiguous.
One reaction zone is a carbon-rich zone 17 in the region of the lance tip 11 of the lance
9, i.e. in an intermediate section of the vessel in terms of height. In this zone the pre-
dominant reactions are oxidising reactions involving combustion of metallised material,
char, coal volatiles, CO, and H2 with oxygen which generate heat, particularly in a hot
zone 51 in the immediate vicinity of the lance tip 11.
The other reaction zone is a metal-rich zone 19 in a lower section of the vessel in which
(a) coal is devolatilised and forms char and coal volatiles and (b) iron ore fines are at
least partially reduced and thereby metallised by CO and H2.
The above-described supply of solids and gases produces an upward flow of fluidising
gas and entrained solids in the central region of the vessel. Increasingly, as the solids
move upwardly, the solids disengage from the upward stream of fluidising gas and flow

downwardly in an annular region between the central region and the side wall of the
vessel. Recirculated solids are either entrained again in the upward stream of fluidis-
ing gas or are discharged from the vessel. The movement of solids transports the sol-
ids through the hot zone 51 and the smaller particles, particularly metallised micron
sized particles become sticky and adhere to other particles, particularly larger particles.
As is indicated above, this agglomeration of smaller particles provides substantial ad-
vantages.
The upward stream of fluidising gas and entrained solids in the central region of the
vessel 3 is countercurrent to the downward flow of oxygen gas and is believed to result
in the entrainment of some of the solids in the oxygen gas; The interaction of the
counter current flows of fluidising gas and oxygen is believed to limit the extent to which
solids entrained in or passing through the oxygen flow can contact vessel surfaces and
cause accretions. The formation of accretions is believed to be further limited due to
the central location of the flow of oxygen gas within the vessel.
The above-described downward flow of solids in the annular region between the central
region and the side wall facilitates transfer of heat from the carbon-rich zone to the
metal-rich zone.
In addition, the downward flow of solids partially shields the side wall from direct expo-
sure to radiant heat from the central region of the vessel.
The above-described process also produces a stream of off-gas and entrained solids
that is discharged from the vessel via an outlet 27 in an upper section of the vessel.
The off-gas stream is processed by separating solids from the off-gas and returning the
separated solids to the vessel via a solids return leg 29. Thereafter, the off-gas is
treated by a series of steps including (a) removal of solids, (b) cooling the off-gas, (c)
H2O removal, (d) CO2 removal, (e) compression, and (f) reheating.
The treated off-gas is thereafter returned to the vessel as part of the fluidising gas.

The above-described process produces a stream of solids, including at least partially
reduced iron ore and char, that is discharged from the vessel via an outlet 25 in the
base of the vessel.
The solids stream may be processed by separating the at least partially reduced iron
ore and at least part of the other solids. The other solids, predominantly char, may be
returned to the vessel as a part of the solids feed for the process. The at least partially
reduced iron ore is further processed as required. By way of example, the at least par-
tially reduced iron ore may be supplied to a molten bath-based smelting vessel and
smelted to molten iron, for example by a process such as the so called "Hlsmelt proc-
ess".
As is indicated above, the present invention was made during the course of an on-
going research project carried out by the applicant to develop CIRCOFER technology
for the direct reduction of iron ore. The research project included a series of pilot plant
runs on 350mm diameter and 700mm diameter pilot plant set-ups of the applicant.
The following discussion focuses on research work on the 700 mm diameter vessel
pilot plant.
The pilot plant comprises an apparatus of the type shown in Figure 1 and 2. The pilot
plant was operated as a circulating fluidised bed at atmospheric pressure. The vessel
has a height of 10.7 m. An upper section of the vessel has a height of approximately
8.9 m and an internal diameter of 700 mm. A lower section of the vessel has a height
of approximately 1.8m and an internal diameter of 500 mm. This height of 1.8 m inclu-
des the height of a fluidising grate and a transition section between the 500 mm diame-
ter and the 700 mm diameter sections. The vessel is refractory lined.
Off-gas from the vessel was processed to remove entrained solids by passing the off-
gas successively through 3 cyclones connected in series. The first cyclone (cyclone 1)
received off-gas directly from the vessel. Solids separated in the cyclone were re-
turned to the vessel via a seal pot that provided for pressure sealing. The second cyc-
lone (cyclone 2) received off-gas from cyclone 1. Solids separated in the cyclone were

returned to the vessel via a direct return of solids (i.e. no seal pot). The third cyclone
(cyclone 3) received off-gas from the second 2. Solids separated by cyclone 3 were
not returned to the vessel.
After solids separation by the three cyclones, the off-gas was further treated by a radial
flow scrubber, which further removed solids from the off-gas. These solids were con-
centrated by a thickener and then passed through a drum filter to produce thickener
sludge.
Off-gas leaving the radial flow scrubber was then treated by a tube cooler that operated
to dewater the off-gas by cooling it to within the range 10-30°C. Following treatment by
the tube cooler, the off-gas was combusted.
The fluidised bed was fluidised by air during the initial stages of testing and was later
fluidised by a mixture of nitrogen and hydrogen gas. As there were no provisions for
processing and recycling the process off-gas, e.g. CO2 removal and compression, it
was not possible for it to be returned to the vessel as fluidising gas. In this regard,
hydrogen gas was used to simulate the effect of using processed off-gas as fluidising
gas.
In summary, the research work demonstrated the following:
The concept of a coal based fluidised bed reduction process with oxygen injection, pro-
ducing a reduced product with metallisation levels of up to 78%.
Injecting oxygen into/or close to a fluidised bed with up to 42% metallic iron in the bed
appears to be feasible without the formation of accretions.
The concept of simultaneously reducing iron ore and partially burning coal for energy in
a single bed vessel appears to be feasible, at metallic iron loadings up to 48% in the
product.

The position of the oxygen lance in the vessel is important because of the desirability of
transferring the heat of oxidation back into the bed while minimising the level of iron re-
oxidation. The 4-m position is about right for the conditions tested.
High phosphorus Brockman iron ore was successfully fluidised and reduced without
excessive dust make. (Brockman ore is a friable West Australian iron ore made avail-
able by Hamersley Iron Pty Ltd, Perth, Western Australia.)
Objectives of the experimental program:
The primary objective was to achieve stable operation for a significant amount of time
with high phosphorus Brockman ore (-3mm) and Blair Athol coal.
The plan was to operate with low iron ore feed (up to 20% in product discharge) for two
days with the oxygen lance in a low position (1.9-m above the distributor plate (not
shown in the Figure) of the vessel. The aim was then to operate for three days with
high ore feed (up to 70% in the product) with the oxygen lance in an upper position
(3.8-m above the distributor plate).
Start-up:
The campaign started on the 9th of December 2003 at 0600 hrs with a gradual heat up
of the 700-mm vessel (hereinafter also referred to as a "CFB") using alumina as the
bed material. Once the target temperature was reached, coal and oxygen were intro-
duced into the vessel at 1550 hrs. The oxygen rate was increased up to 105 Nm3/hr
while the coal rate was in the range 300-450 kg/hr.
Operation with coal and oxygen 10/12/03 - 11/12/03
Operation with coal, air and oxygen was conducted on 10/12/03. The operation was
very smooth with the system stabilising fairly quickly and the vessel maintaining its
temperature of 900-930°C without any problems.

The standard operating conditions during this period were as follows.
CFB temperature: 930°C bottom and 900°C top
Fluidising gas flowrate: 140Nm3/hr (N2) and 300Nm3/hr (air)
Pressure drop CFB: 80-140 mbar
Oxygen flowrate: up to 100 Nm3/hr
N2 shield gas flowrate: 30 Nm3/hr
Coal Feed Rate: 340-450 kg/hr
A summary of the results is as follows:
Bed Discharge Rate: 100-160 kg/hr
Cyclone 3 Discharge: 10-14 kg/hr
Offgas Analysis

The discharge product was clean with only some small +2mm pieces which looked like
residual refractory material. The dust make was reasonably low with charge reporting to the final cyclone discharge.
Operation with Iron Ore (10-140 kg/hr), Coal and Oxygen (lance 2-m height) 10/12/03 -
12/12/03
10/12/03 2200 - 11/12/03 0600: Iron Ore at 10 kg/hr
Iron ore ( 10 kg-hr. Hydrogen was also introduced into the fluidising gas at a rate of 20 Nm3/hr to
simulate use of processed off-gas as fluidising gas. The operation was smooth with the
bed AP being maintained at about 100-120 mbar and the temperature profile having a
range of only 10°C between the bottom and the top of the bed.

The product appeared fine without any signs of accretions or agglomerates. However,
on screening the product (at 2mm) some larger scale type material was found but this
was only a very small proportion of the overall product. The scale appeared to be
made up of ash/char and probably formed on the walls of the vessel or distributor plate
in the vessel.
The standard operating conditions and results during this period were as follows.
CFB temperatures: 930°C bottom and 900°C top
Fluidising gas flowrate: 350 Nm3/hr (N2) and 20 Nm3/hr (H2)
Pressure drop CFB: 100-130 mbar
Oxygen flowrate: 100-115 Nm3/hr
N2 shield gas flowrate: 30 Nm3/hr
Coal Feed Rate: 280-360 kg/hr
Iron Ore Feed Rate: 10 kg/hr
A summary of the results is as follows:
Bed Discharge Rate: 125 kg/hr
Cyclone Discharge: 15 kg/hr
Offgas Analysis

11/12/13 0600 - 11/12/03 1200: Iron Ore at 20 kg/hr
The iron ore feed rate was increased up to 20 kg/hr at 0600 on 11/12/03 until 1200
11/12/03 and the hydrogen gas rate was also increased up to 40 Nm3/hr. The operation
continued to be smooth without any disruptions. The vessel bed pressure was being

maintained at about 80-100 mbar and the temperature profile had a range of only 10°C
between the bottom and the top of the bed.
The appearance of the product continued to be good without any signs of accretions or
agglomerates. As before the only exception to this was the odd piece of scale type
material, which appeared to be composed of ash/char.
The standard operating conditions and results during this period were as follows.
CFB temperatures: 952°C bottom and 940°C top
Fluidising gas flowrate: 350 Nm3/hr (N2) and 40 Nm3/hr
Pressure drop CFB: 80-100 mbar
Oxygen flowrate: 112 Nm3/hr
N2 shield gas flowrate: 30 Nm3/hr
Coal Feed Rate: 430 kg/hr
iron Ore Feed Rate: 20 kg/hr
A summary of the results is as follows:
Bed Discharge Rate: 125 kg/hr
Cyclone 3 Discharge: 15 kg/hr
Offgas Analysis

Product Analysis: (0900 11/12/03)


11/12/03 1200 - 12/12/03 0600: Iron Ore at 40 kg/hr
Summary:
The iron ore feed rate was increased up to 40 kg/hr at 1200 on 11/12/03 and operated
with this rate until 0600 12/12/03, while the hydrogen gas rate was maintained at 40
Nm3/hr and the coal rate was around 360-420 kg/hr. The operation continued to be
smooth without any disruptions and the iron product discharge was highly metallised.
Dust make was also low with less than 10% of the total discharge coming from the final
cyclone (i.e. cyclone 3). The vessel bed AP was being maintained at about 90-135
mbar and the temperature profile had a range of less than 10°C between the bottom
and the top of the bed.
Results
The appearance of the product continued to be good without any signs of accretions or
agglomerates.
The standard operating conditions and results during this period were as follows.
CFB temperatures: 953°C bottom and 941 °C top
Fluidising gas flowrate: 370 Nm3/hr (N2) and 40 Nm3/hr (H2)
Pressure drop CFB: 98-130 mbar
Oxygen flowrate: 113 Nm3/hr
N2 shield gas flowrate: 30 Nm3 /hr
Coal Feed Rate: 426 kg/hr
Iron Ore Feed Rate: 40 kg/hr
A summary of the results is as follows:
Bed Discharge Rate: 190-210 kg/hr
Cyclone 3 Discharge: 15-20 kg/hr
Offgas Analysis


The high metallisation achieved (70-77%) indicates that the oxygen lance (even at its
1.9-m position) did not penetrate too far to the bottom of the bed and that there was
good segregation within the bed. The lower part of the bed is iron rich. The higher part
of the bed is carbon rich and this is interacting with the oxygen lance to generate heat
and this heat is then transferred back into the bed by the recirculation of the solids to
the lower parts of the bed. The low CO/CO2 ratio in the off-gas indicates achievement
of high post combustion, with the energy levels being transferred back into the bed,
while maintaining high metallisation levels in the product discharge.

The iron levels in the product and the degree of metallisation indicates that the 700-mm
vessel can be operated in gasification mode with up to 20-25% metallic iron content
without any problems with accretions. This is a significant achievement.
Oxygen Lance Inspection (12/12/03)
The lance was taken out of the 700-mm vessel and inspected on 12/12/03.
In summary, the lance was clean. The water cooled pipe as well as the nozzle tip had
no evidence of any buildup of material.
The lance was repositioned in the vessel at a higher position i.e. 3.8-m above the dis-
tributor plate. The vessel was restarted with coal and oxygen and then once stabilised
iron ore and hydrogen.
Operation with Iron Ore (110-200 kg/hr). Coal and Oxygen (lance 4-m height) 13/12/03
-16/12/03
13/12/03 0600 - 13/12/03 1200: Iron Ore at 110 kg/hr
Summary;
The iron ore feed rate was increased stepwise up to 110 kg/hr at 0625 on 13/12/03 and
operated with this rate until 1200 13/12/03 while the hydrogen gas rate was also in-
creased stepwise up to 110 Nm3/hr over a 2 hr period. The coal rate was around 360-
400 kg/hr. The operation continued to be smooth without any disruptions and the iron
product discharge from the vessel was up to 78% metallised. Dust make was also low
with vessel bed AP was being maintained at about 90-135 mbar and the temperature profile
had a range of less than 5°C between the bottom and the top of the bed.
Increasing the lance height from 1.9m to 3.8m did not seem to impact on the bed tem-
perature profile. In fact, the temperature spread was less than 5°C from top to bottom.

Results:
The appearance of the product continued to be good without any signs of accretions or
agglomerates.
The standard operating conditions and results during this period were as follows.
CFB temperatures: 953°C bottom and 951°C top
Ruidising gas flowrate CFB 10 Nm3/hr (N2) at 860°C, 110 Nm3/hr (N2) at 740°C, 180
Nm3/hr (N2) at 680°C. and 110 Nm3/hr (H2) at 860°C
Pressure drop CFB: 80-100 mbar
Oxygen flowrate: 110 Nm3 /hr
N2 shield gas flowrate: 30-40 Nm3/hr
Coal Feed Rate: 360-400 kg/hr
Iron Ore Feed Rate: 110 kg/hr
A summary of the results is as follows:
Bed Discharge Rate: 162 kg/hr
Cyclone 3 Discharge: 16 kg/hr
Offgas Analysis


With the higher oxygen lance position the uniform bed temperature profile of the lower
lance was maintained. This indicates that even with the oxygen lance at the 3.8m posi-
tion the solids recirculation profile is such that enough heat is transferred back into the
bottom of the bed.
The temperature profile in the vessel and the cyclones indicated that there was proba-
bly no increase in dust make with the increase in iron ore feed rate up to 110 kg/hr.
The discharge from the final cyclone relative to the vessel also did not change signifi-
cantly. This suggests that either the iron ore is not breaking down as much as predicted
or that any fines generated are re-agglomerated in the high temperature region of the
oxygen lance.
13/12/03 1200-16/12/03 0500: Iron Ore at 120 - 230 kg/hr
Summary:
For the first period of this operation from 17:00 13/12/03 to 12:00 15/12/03 the opera-
tion rate was approximately 120 kg/h iron ore feed. This included a period of distur-
bance where there was no feed. The final period operated at approximately 230 kg/h
iron ore feed.
The operation with 230 kg/hr iron ore feed rate was smooth without any disruptions and
the iron product discharge from the CFB ranged from 48% to 78% metallised. Dust
make was also low at bed AP was being maintained at about 80-100 mbar and the temperature profile range
had now increased to about 20°C between the bottom and the top of the bed.
Operating the vessel at the higher iron ore feed rate of 200 kg/hr increased the range of
the CFB temperature profile with the bottom part of the bed now being up to 20°C
colder than the middle of the bed. The metallisation levels were also lower at the
higher iron ore feed rates but they were still in the 60-80% metallisation range.

Results:
The appearance of the product continued to be good without any signs of accretions or
agglomerates.
The standard operating conditions and results during this period were as follows.
CFB temperatures: 947°C bottom and 960°C top
FB gas heater temperature: 740°C and 615°C main heater
Fluidising gas flowrate CFB: 20 Nm3/hr (N2) at 840°C, 100 20 Nm3/hr (N2) at 740°C,
185 20 Nm3/hr (N2) at 615°C, and 140 Nm3/hr (H2) @ 840°C
Pressure drop CFB: 83-96 mbar
Oxygen flowrate: 113 Nm3/hr
N2 shield gas flowrate: 30-40 Nm3/hr
Coal Feed Rate: 380 kg/hr
Iron Ore Feed Rate: 200 kg/hr
A summary of the results is as follows:
Bed Discharge Rate: 227-286 kg/hr
Cyclone 3 Discharge: 18-24 kg/hr
Offgas Analysis (0400 hrs 15/12/03)




At the high iron ore feed rates (200 kg/hr) the discharge from the vessel increased sig-
nificantly while the discharge from the final cyclone only increased slightly. However,
the discharge from the final cyclone relative to the vessel did not seem to change. It
was further observed that the amount of fines the amount of fines breaking down as much as predicted or that any fines generated are re-agglomerated
in the high temperature region of the oxygen lance. The temperature profile through
the cyclones also supports this since there were no significant increases in tempera-
tures through the cyclone system at the higher iron ore feed rates. The product metal-
lisation levels were maintained in the range of 68-78% during the high iron ore feed
rates while the product discharge had up to 48% metallic iron.
Oxygen Lance and Vessel Inspection (16/12/03 and 19/12/03)
The lance was taken out of the 700-mm vessel and inspected on 16/12/03. In sum-
mary, the lance was fairly clean. The water cooled pipe had a thin coating of material
while the nozzle tip was relatively clean. The nature of the build up (flaky and thin)
suggested that this would not lead to any operational problems.
Iron Distribution & Agglomeration
Analysis of the Brockman ore sample used as feed to the fluidised bed indicated a fines
content of approximately 10.6% sub 45 micron. These units were expected to appear
as output from cyclone 3 or as thickener sludge. Due to the friable nature of Brockman
Ore, it was expected that additional fines would be produced during processing. It was
therefore expected that the percentage of iron units exiting the system through cyclone
3 would exceed 10.6%.
It was observed that approximately 7% of the iron units input to the fluidised bed were
discharged through cyclone 3, either as direct output from cyclone 3 (approximately
4%) or as output from the radial flow scrubber (approximately 3%). Analysis of the
main product output from the fluidised bed indicated that an agglomeration mechanism
was present within the process. This mechanism appeared to be primarily smaller par-

tides, typically sub 100 micron particles, agglomerating to each other and to larger par-
ticles.
Many modifications may be made to the embodiments of the present invention shown
in the Figure without departing from the spirit and scope of the invention.

We claim :
1. A circulating fluidized bed process for direct reduction of a solid metalliferous material
having a particle size distribution that at least in part comprises micron sized particles, said process
comprising:
supplying the metalliferous material, a solid carbonaceous material, an oxygen-rich gas and
a fluidizing gas to a vessel, whereby a fluidized bed is maintained in the vessel, the fluidized bed
containing a carbon-rich zone, withdrawing gas and entrained solids from an upper section of the
vessel, separating solids from the withdrawn gas, and recirculating the separated solids to the vessel,
and
discharging a product stream from a lower section of the vessel,
wherein the step of supplying the oxygen-rich gas comprises injecting the oxygen-rich gas
downwardly into the carbon-rich zone using a cooled lance spaced horizontally inward from side walls
of the vessel, whereby heat is generated in the carbon-rich zone by reactions between oxygen and
metallized material, the solid carbonaceous material and other oxidizable solids and gases in the
fluidized bed, metalliferous material is at least partially reduced in a metal-rich zone below the carbon-
rich zone, and the product stream discharged from the vessel comprises the at least partially reduced
metalliferous material, and
wherein the process involves controlling agglomeration of particles by adjusting at least
one of feed rate of the metalliferous material, feed rate of the carbonaceous material and feed rate of
the oxygen-rich gas.
2. A process as claimed in claim 1, wherein the metalliferous material is supplied in the
form of fines.
3. A process as claimed in claim 1, wherein the metalliferous material is supplied in the form
of iron ore fines sized at minus 6 mm.
4. A process as claimed in claim 1, wherein the metalliferous material is supplied in the form
of fines having an average particle size in the range from 0.1 to 0.8 mm.

5. A process as claimed in claim 1, wherein the metalliferous material is supplied to the
vessel with a selected maximum particle size and controlling agglomeration of the particles so that 90%
of the particles discharged from the lower section of the vessel as the product stream do not exceed the
selected maximum particle size.
6. A process as claimed in claim 1, wherein the metalliferous material is supplied to the
vessel with a selected maximum particle size and controlling agglomeration of the particles so that no
more than 30% by weight of the total weight of iron units discharged from the process is carried off in
an off-gas stream from the process.
7. A process as claimed in any of claims 1 to 6, wherein the oxygen-rich gas is injected using
a lance having a tip directed downward at up to 40 degrees from vertical, preferably at up to 15 degrees
from vertical.
8. A process as claimed in claim7, wherein the lance is water cooled.
9. A process as claimed in any of claims 1 to 6, wherein the lance has a central pipe and the
oxygen-rich gas is supplied through the central pipe of the lance.
10. A process as claimed in any of claims 1 to 6, wherein the lance has a lance tip and the
oxygen-rich gas is supplied with sufficient velocity such that a substantially solids-free zone is formed
in the region of the lance tip, whereby formation of accretions that could block injection of the oxygen-
rich gas is minimized.
11. A process as claimed in claim10, wherein the lance has a lance tip and the oxygen-rich gas
is injected with a velocity in the range 50-300 m/s.
12. A process as claimed in any of claims 1 to 6, wherein the lance has a lance tip and a
shrouding gas is injected for shrouding a region of the lance tip.

13. A process as claimed in claim 12, wherein the shrouding gas is injected into the vessel
with a velocity at least 60% of the velocity of the oxygen-rich gas.
14. A process as claimed in any of claimsl to 6, wherein the lance has a lance tip that is spaced
inwardly of side walls of the vessels and has a central pipe, and the lance also has an outer surface, and
the oxygen-rich gas is injected through the central pipe and the outer surface of the lance is water
cooled.
15. A process as claimed in any of claims1 to 6, wherein solids and fluidizing gas are supplied
to the vessel in a manner such that the solids pass through the carbon-rich zone and the reducing zone.
16. A process as claimed in any of claims1 to 6, wherein the fluidized bed is maintained by
supplying a downward flow of the oxygen-rich gas,an upward flow of solids and the fluidizing gas
countercurrent to the downward flow of the oxygen-rich gas, and a downward flow of solids outward
of the upward flow of solids and the oxygen-rich gas.
17. A process as claimed in claim 16, wherein the heat generated in the carbon-rich zone by the
reactions between oxygen and metallized material, the solid carbonaceous material and other
oxidizable solids and gases, heats the solids in the upward and downward flows of solids, whereby
solids in the downward flow of solids transfer heat to the metal-rich zone.
18. A process as claimed in claim 16, wherein the upward and downward flows of solids shield
the side wall of the vessel from radiant heat generated by reactions between the oxygen-containing gas
and the solid carbonaceous material and other oxidizable solids and gases in the fluidized bed.
19. A process as claimed in any of the preceding claims, wherein the carbonaceous material is
coal.
20. A process as claimed in any of the preceding claims, wherein the fluidizing gas comprises a
reducing gas.

21. A process as claimed in claim 20, wherein the fluidizing gas comprises CO and H2 and the
amount of H2 in the fluidizing gas is at least 15% by volume of the total volume of CO and H2 in the
gas.
22. A process as claimed in any of the preceding claims, wherein the product stream comprises
solids other than the at least partially reduced metalliferous material, and at least a portion of the other
solids is separated from the product stream.
23. A process as claimed in claim 22, wherein at least a portion of the other solids is returned to
the vessel.
24. A process as claimed in any of the preceding claims, wherein the separated solids are
recirculated to the lower section of the vessel.
25. A process as claimed in any of the preceding claims, wherein metalliferous material supplied
to the vessel is preheated with gas withdrawn from the upper section of the vessel.
26. A process as claimed in claim 25, wherein the gas withdrawn from the upper section of the
vessel is is treated and the treated gas is returned to the vessel as fluidizing gas.
27. A process as claimed in claim26, wherein the gas withdrawn from the upper section of the
vessel is treated by at least one of (a) solids removal, (b) cooling, (c) H2O removal, (d) CO2 removal,
(e) compression, and (f) reheating.
28. A process as claimed in claim 26, wherein the gas withdrawn from the upper section of the
vessel is treated by solids removal, the treated gas is returned to the vessel as fluidizing gas, and the
removed solids are returned to the vessel.
29. A process as claimed in claim 1, wherein the fluidizing gas contains a reducing gas and
more than 50% of the metalliferous material is reduced.

30. A process as claimed in any of the preceding claims, wherein the oxygen-rich gas
comprises at least 90% by volume oxygen.
31. A process as claimed in any of the preceding claims, wherein reducing gases are released
from the carbonaceous material in the carbon-rich zone and the reducing gases react with metalliferous
material in the metal-rich zone.
32. A process as claimed in claim 1, wherein the metalliferous material is supplied to the
vessel with a selected maximum particle size and agglomeration of the particles is controlled so that no
more than 20% by weight of the total weight of iron units discharged from the process is carried off in
an off-gas stream from the process.
33. A process as claimed in claim 1, wherein the metalliferous material is supplied to the
vessel with a selected maximum particle size and agglomeration of the particles is controlled so that no
more than 10% by weight of the total weight of iron units discharged from the process is carried off in
an off-gas stream from the process.


A direct reduction process for a solid metalliferous material having a particle size distribution that at least in part comprises
micron sized particles, comprises supplying the metalliferous material, a solid carbonaceous material, an oxygen-containing
gas, and a fluidizing gas into a fluidized bed in a vessel and maintaining the fluidized bed in the vessel, at least partially reducing
metalliferous material in the vessel, and discharging a product stream that comprises the at least partially reduced metalliferous
material from the vessel. The process is characterized by: (a) establishing and maintaining a carbon-rich zone within the fluidized
bed; (b) passing metalliferous material, including metallised material (which term includes partially metallised material), through
the carbon-rich zone; and (c) injecting the oxygen-containing gas into the carbon-rich zone and oxidizing metallised material, solid
carbonaceous material and other oxidisable solids and gases and causing controlled agglomeration of particles.

Documents:

03174-kolnp-2006 abstract.pdf

03174-kolnp-2006 claims.pdf

03174-kolnp-2006 correspondence others.pdf

03174-kolnp-2006 description(complete).pdf

03174-kolnp-2006 drawings.pdf

03174-kolnp-2006 form-1.pdf

03174-kolnp-2006 form-3.pdf

03174-kolnp-2006 form-5.pdf

03174-kolnp-2006 international publication.pdf

03174-kolnp-2006 pct others.pdf

03174-kolnp-2006-assignment.pdf

03174-kolnp-2006-correspondence others-1.1.pdf

03174-kolnp-2006-pct others-1.1.pdf

03174-kolnp-2006-priority document.pdf

3174-kolnp-2006-abstract.pdf

3174-kolnp-2006-amanded claims.pdf

3174-KOLNP-2006-ASSIGNMENT.pdf

3174-KOLNP-2006-CORRESPONDENCE 1.1.pdf

3174-KOLNP-2006-CORRESPONDENCE-1.2.pdf

3174-kolnp-2006-description (complete).pdf

3174-kolnp-2006-drawings.pdf

3174-KOLNP-2006-Examination Report Reply Recieved.pdf

3174-KOLNP-2006-EXAMINATION REPORT.pdf

3174-kolnp-2006-form 1.pdf

3174-KOLNP-2006-FORM 18-1.1.pdf

3174-kolnp-2006-form 18.pdf

3174-kolnp-2006-form 2.pdf

3174-KOLNP-2006-FORM 3-1.1.pdf

3174-kolnp-2006-form 3.pdf

3174-KOLNP-2006-FORM 5.pdf

3174-KOLNP-2006-GPA.pdf

3174-KOLNP-2006-GRANTED-ABSTRACT.pdf

3174-KOLNP-2006-GRANTED-CLAIMS.pdf

3174-KOLNP-2006-GRANTED-DESCRIPTION (COMPLETE).pdf

3174-KOLNP-2006-GRANTED-DRAWINGS.pdf

3174-KOLNP-2006-GRANTED-FORM 1.pdf

3174-KOLNP-2006-GRANTED-FORM 2.pdf

3174-KOLNP-2006-GRANTED-SPECIFICATION.pdf

3174-kolnp-2006-others 1.1.pdf

3174-KOLNP-2006-OTHERS-1.1.pdf

3174-KOLNP-2006-OTHERS.pdf

3174-kolnp-2006-pa.pdf

3174-KOLNP-2006-PETITION UNDER RULE 137-1.1.pdf

3174-KOLNP-2006-PETITION UNDER RULE 137.pdf

3174-kolnp-2006-reply to examination report 1.1.pdf

3174-KOLNP-2006-REPLY TO EXAMINATION REPORT-1.2.pdf


Patent Number 251596
Indian Patent Application Number 3174/KOLNP/2006
PG Journal Number 13/2012
Publication Date 30-Mar-2012
Grant Date 26-Mar-2012
Date of Filing 31-Oct-2006
Name of Patentee OUTOKUMPU TECHNOLOGY OYJ
Applicant Address RIIHITONTUNTIE 7, FI-02200 ESPOO, FINLAND
Inventors:
# Inventor's Name Inventor's Address
1 ORTH ANDREAS OBERE ROMERHOFSTRASSE 132, 61381 FRIEDRICHSDORF, GERMANY
2 PHILP DONALD KEITH (DECEASED) 1 SHERBROOK GARDENS,BIBRA LAKE, W.A.6163, AUSTRALIA
3 DRY ROD 326 THE BOULEVARD, CITY BEACH,W.A. AUSTRALIA
4 EICHBERGER HEINZ AM HAAG 12J, 65812 BAD SODEN, GERMANY
PCT International Classification Number C21B 13/00
PCT International Application Number PCT/EP2005/005465
PCT International Filing date 2005-05-20
PCT Conventions:
# PCT Application Number Date of Convention Priority Country
1 2004902898 2004-05-31 Australia