TECHNICAL FIELD
[0001] This disclosure relates to quasiparticles for sintering that are used as raw material
for sintering to be placed on a palette of, e.g. a downward suction-type Dwight Lloyd
sintering machine, for the purpose of producing sintered ore for blast furnaces, and
to a method of producing the same.
BACKGROUND
[0002] In general, sintered ore that is used as raw material for blast furnaces is produced
by a sintering raw material processing method as follows. Firstly, for example, as
illustrated in FIG. 1, iron ore with a particle size of 10 mm or less, SiO
2-containing raw material with a particle size of 10 mm or less that is formed of silica
stone, serpentinite, nickel slag, or the like, limestone-based raw material that contains
powder CaO, and powder coke or solid fuel-based raw material such as anthracite as
heat source, are placed in a drum mixer with addition of a suitable amount of water,
then mixed and granulated to form granulated products called quasiparticles. Such
mixed raw materials formed of the granulated products are charged on a palette of
a Dwight Lloyd sintering machine to a suitable thickness, e.g. 500 mm to 700 mm, solid
fuel in the surface layer is ignited, and after the ignition solid fuel is combusted
while air is drawn downwardly. Consequently the mixed sintering raw materials are
sintered by the heat of combustion, and sinter cake is formed. The sinter cake is
crushed into uniformly-sized particles to obtain sintered ore with a particle size
equal to or larger than a predetermined size. Other sintered ore with a smaller particle
size is return ore, which is reusable as sintering raw material.
[0003] It is important for such sintered ore thus produced to exhibit, among other things,
good reducibility, which greatly affects blast furnace operations. Reducibility of
sintered ore is normally defined by JIS M8713 ("JIS" stands for Japanese Industrial
Standard), and is denoted herein as JIS-RI. As illustrated in FIG. 2, there is a positive
correlation between reducibility of sintered ore (JIS-RI) and gas utilization rate
in a blast furnace (ηco) and, as illustrated in FIG. 3, there is a negative correlation
between gas utilization rate and fuel ratio in a blast furnace. From this follows
that reducibility of sintered ore (JIS-RI) has a good negative correlation with fuel
ratio via gas utilization rate (ηco) in a blast furnace, and accordingly fuel ratio
will decrease as reducibility of sintered ore improves in the blast furnace.
It this regard, gas utilization rate (ηco) and fuel ratio are defined as:
ηco = CO
2 (%)/(CO (%) + CO
2 (%))
, where CO
2 (%) and CO (%) are both concentrations expressed in volume percent in the gas at
the furnace top of the blast furnace.

[0004] Cold strength of sintered ore is also an important factor in guaranteeing permeability
in a blast furnace. Individual blast furnaces have lower limits on cold strength for
proper operation.
Therefore, sintered ore that has excellent reducibility and high cold strength is
desirable as blast furnace raw material.
In this respect, Table 1 lists the reducibility and tensile strength (cold strength)
of primary mineral structures forming sintered ore, calcium ferrite (CF): nCaO·Fe
2O
3, hematite (He): Fe
2O
3, FeO-containing calcium silicate (CS): CaO·xFeO·y SiO
2, and magnetite (Mg): Fe
3O
4. Note that tensile strength was measured by subjecting disk-shaped ore test pieces
to splitting tensile test (radial compression test or Brazilian test). As can be seen
from Table 1, hematite (He) shows high reducibility and calcium ferrite (CF) has high
tensile strength.
[Table 1]
[0005]
Table 1
|
Calcium Ferrite (CF) |
Hematite (He) |
Calcium Silicate (CS) |
Magnetite (Mg) |
Reducibility (%) |
34 |
50 |
3 |
27 |
Tensile Strength (MPa) |
102 |
49 |
19 |
58 |
[0006] Therefore, a sintering structure that is suitable for sintered ore is obtained by,
as schematically illustrated in FIG. 4, forming calcium ferrite (CF), which is high
in strength, on the surface of a lump and forming hematite (He), which is high in
reducibility, inside the lump. It is preferable for such sintering structure to minimize
the formation of FeO-containing calcium silicate (CS) low in reducibility and strength.
In most conventional sintering machines, however, iron ore, SiO
2-containing raw material, limestone-based raw material, and solid fuel-based raw material
are mixed at the same time as mentioned above and, as a consequence, in a quasiparticle
structure obtained by mixing and granulating raw materials as illustrated in FIG.
5, powder ore, lime, and coke are present, in a mixed manner, on the circumference
of coarse core ore. A sintered ore structure obtained by sintering such quasiparticles
will include a mixture of four types of mineral structures: hematite (He), calcium
ferrite (CF), calcium silicate (CS) containing FeO, and magnetite (Mg).
[0007] In such a situation, many attempts have been made to form more calcium ferrite (CF)
and hematite (He). For example, considering the fact that FeO-containing calcium silicate
(CS) forms more when sintered at high temperature, one technique is described in JPS63149331A
(PTL 1) that involves granulating powder iron ore with addition of a binder or limestone,
coating the surfaces of the granules with coke breeze as heat source to increase combustibility
of coke, and performing sintering at low temperature to improve reducibility.
[0008] According to the conventional method proposed, however, CaO reside in close proximity
to SiO
2 or SiO
2-based raw material in the iron-based raw material, which fact inevitably generates
a large amount of FeO-containing calcium silicate (CS). Consequently, a structure
that is formed mainly of calcium ferrite (CF) and hematite (He) may not always be
provided.
[0009] To address the above problem,
WO2001092588A (PTL 2) describes that by using as raw material such quasiparticles that does not
require any large-scale apparatus as pretreatment for producing sintered ore and that
have a layered structure in which iron ore raw material is separated from limestone-based
raw material and solid fuel-based raw material, it becomes possible to produce sintered
ore having the structure such that calcium ferrite (CF) with high strength is selectively
formed on the surface of the sintered ore and hematite (He) with high reducibility
is selectively formed on the inside of the sintered ore, and the sintered ore thus
obtained exhibits improved cold strength and improved reducibility.
CITATION LIST
Patent Literature
SUMMARY
(Technical Problem)
[0011] With the technique described in PTL 2, as illustrated in FIG. 6, if iron ore and
SiO
2-containing raw material, each containing SiO
2 in large quantities, are used with quasiparticles that are separated from limestone-based
raw material and from solid fuel-based raw material, in production of sintered ore,
it becomes possible to delay reaction between CaO and SiO
2 during a sintering process, thereby reducing formation of calcium silicate (CS) containing
FeO, which is poor in reducibility and low in cold strength. The resulting sintered
ore has the structure such that calcium ferrite (CF) with high strength is selectively
formed on the surface of the sintered ore and hematite (He) with high reducibility
is selectively formed on the inside of the sintered ore.
[0012] By applying the quasiparticles for sintering as described in PTL 2, sintered ore
with excellent reducibility and high cold strength can be obtained. To achieve, however,
low-reduction-agent-ratio operations of blast furnaces (low RAR (Reduction Agent Ratio)
operations are operations with a reduction in the total amount of reducing agents
blown in from tuyeres and coke charged in from the furnace top per 1 t of produced
pig iron) by further improving reducibility of sintered ore in blast furnaces, there
is a need for further improvement of reducibility (JIS-RI) of sintered ore.
(Solution to Problem)
[0013] Upon carefully examining, in particular, the way of improving reducibility of sintered
ore that is produced with quasiparticles for sintering having a layered structure
that are obtained by separating iron ore raw material from limestone-based raw material
and from solid fuel-based raw material, we newly discovered that to include an alkali
metal in iron ore raw material within a particular range is effective for increasing
the advantages of quasiparticles for sintering having a layered structure.
[0014] We thus provide:
- 1. A quasiparticle for sintering comprising, at least, iron ore raw material, limestone-based
raw material, and solid fuel-based raw material, each being used to produce sintered
ore for blast furnaces,
wherein the iron ore raw material forms a core of the quasiparticle, and the limestone-based
raw material and the solid fuel-based raw material are coated on the circumference
of the core, and
wherein the core formed of the iron ore raw material contains high-alkaline iron ore
having an alkali metal content of 0.05 mass% or more.
In this case, examples of the alkali metal include lithium, sodium, potassium, rubidium,
and cesium; among these, sodium and potassium are suitably used as the iron ore raw
material for sintered ore.
- 2. The quasiparticle for sintering according to aspect 1, wherein the core formed
of the iron ore raw material comprises:
a first layer that is formed of general iron ore having an alkali metal content of
less than 0.05 mass%; and
a second layer that is formed of the high-alkaline iron ore having an alkali metal
content of 0.05 mass% or more and that covers the surface of the first layer.
- 3. The quasiparticle for sintering according to aspect 1, wherein the core formed
of the iron ore raw material comprises:
a first layer that is formed of the high-alkaline iron ore having an alkali metal
content of 0.05 mass% or more; and
a second layer that is formed of the general iron ore having an alkali metal content
of less than 0.05 mass% and that covers the surface of the first layer.
- 4. The quasiparticle for sintering according to any one of aspects 1 to 3, wherein
the iron ore raw material contains the high-alkaline iron ore having an alkali metal
content of 0.05 mass% or more in an amount of 20 mass% or more.
- 5. The quasiparticle for sintering according to any one of aspects 1 to 4, wherein
the high-alkaline iron ore having an alkali metal content of 0.05 mass% or more has
a mean particle size of 2 mm or more, and the general iron ore having an alkali metal
content of less than 0.05 mass% has a mean particle size of less than 2 mm.
- 6. The quasiparticle for sintering according to any one of aspects 1 to 5, wherein
the alkali metal content of the high-alkaline iron ore having an alkali metal content
of 0.05 mass% or more is 0.30 mass% or less.
- 7. The quasiparticle for sintering according to any one of aspects 1 to 6, wherein
the limestone-based raw material and the solid fuel-based raw material are coated
layer-by-layer on the circumference of the core.
- 8. The quasiparticle for sintering according to any one of aspects 1 to 7, wherein
a mixed layer of the limestone-based raw material and the solid fuel-based raw material
is coated on the circumference of the core.
- 9. A method of producing a quasiparticle for sintering, the method comprising:
when mixing and granulating, at least, iron ore raw material, limestone-based raw
material, and solid fuel-based raw material, each being used to produce sintered ore
for blast furnaces,
mixing and granulating the iron ore raw material containing high-alkaline iron ore
having an alkali metal content of 0.05 mass% or more to obtain a granulated particle;
and
causing the limestone-based raw material and the solid fuel-based raw material to
be adhered to the granulated particle and, subsequently, performing granulation.
- 10. A method of producing a quasiparticle for sintering, the method comprising:
when mixing and granulating, at least, iron ore raw material, limestone-based raw
material, and solid fuel-based raw material, each being used to produce sintered ore
for blast furnaces,
mixing and granulating general iron ore having an alkali metal content of less than
0.05 mass% and SiO2-containing raw material to form a first layer;
causing high-alkaline iron ore having an alkali metal content of 0.05 mass% or more
to be adhered to the surface of the first layer, and subsequently performing granulation
to form a second layer; and
causing the limestone-based raw material and the solid fuel-based raw material to
be adhered to the surface of the second layer and, subsequently, performing granulation.
- 11. A method of producing a quasiparticle for sintering, the method comprising:
when mixing and granulating, at least, iron ore raw material, limestone-based raw
material, and solid fuel-based raw material, each being used to produce sintered ore
for blast furnaces,
mixing and granulating high-alkaline iron ore having an alkali metal content of 0.05
mass% or more to form a first layer;
causing general iron ore having an alkali metal content of less than 0.05 mass% to
be adhered to the surface of the first layer, and subsequently performing granulation
to form a second layer; and
causing the limestone-based raw material and the solid fuel-based raw material to
be adhered to the surface of the second layer and, subsequently, performing granulation.
- 12. The method of producing a quasiparticle for sintering according to any one of
aspects 7 to 11, wherein the high-alkaline iron ore having an alkali metal content
of 0.05 mass% or more has a mean particle size of 2 mm or more, and the general iron
ore having an alkali metal content of less than 0.05 mass% has a mean particle size
of less than 2 mm.
- 13. The method of producing a quasiparticle for sintering according to any one of
aspects 7 to 12, wherein mixed powder of the limestone-based raw material and the
solid fuel-based raw material is adhered and, subsequently, granulation is performed.
- 14. The method of producing a quasiparticle for sintering according to any one of
aspects 7 to 12, wherein after the adhering of the limestone-based raw material, the
solid fuel-based raw material is adhered to an outer surface of a layer of the limestone-based
raw material and, subsequently, granulation is performed.
(Advantageous Effect)
[0015] According to the present disclosure, it is possible to provide quasiparticles that
are optimal raw material for achieving further improvement of reducibility of sintered
ore.
BRIEF DESCRIPTION OF THE DRAWING
[0016] In the accompanying drawings:
FIG. 1 is a diagram illustrating the flow of mixture and granulation of sintering
raw material in a conventional example;
FIG. 2 is a graph illustrating the relation between reducibility JIS-RI (%) of sintered
ore and gas utilization rate ηco (%) in a blast furnace;
FIG. 3 is a graph illustrating the relation between gas utilization rate ηco (%) and
fuel ratio (kg/t-pig) in a blast furnace;
FIG. 4 illustrates a desirable sintered ore structure;
FIG. 5 illustrates a conventional quasiparticle structure and a conventional sintered
ore structure;
FIG. 6 illustrates a conventionally desirable quasiparticle structure;
FIG. 7 illustrates a basic quasiparticle structure according to the disclosure;
FIG. 8 illustrates a flow (process A) of mixture and granulation of sintering raw
material according to the disclosure;
FIG. 9 illustrates a flow (process B) of mixture and granulation of sintering raw
material according to the disclosure; and
FIG. 10 illustrates a flow (process C) of mixture and granulation of sintering raw
material according to the disclosure.
DETAILED DESCRIPTION
[0017] In the following, quasiparticles for sintering according to the disclosure are described
in detail with reference to the accompanying drawings.
[0018] As quasiparticles for sintering used to produce sintered ore with excellent reducibility
and high cold strength, quasiparticles for sintering contain at least iron ore raw
material, limestone-based raw material, and solid fuel-based raw material, and have
a basic structure, as illustrated in FIG. 7, such that the iron ore raw material is
contained as core 1, and layer 2 formed of the limestone-based raw material and solid
fuel-based raw material is coated on the circumference of core 1.
[0019] In other words, such quasiparticles can be produced by containing iron ore raw material
as core 1 in a state in which core 1 is separated from limestone-based raw material
and does not contain limestone. Layer 2, which is formed of limestone-based raw material
and solid fuel-based raw material and which covers the surface of core 1, enables
a calcium ferrite (CF)-based melt to be formed during a sintering process at the interface
between limestone-based raw material and iron ore so that the CF covers the circumference
of the iron ore, thereby providing sufficient cold strength. The sintered ore that
is obtained by using the above quasiparticles for sintering as sintering raw material
has calcium ferrite (CF) with high strength on the surface and hematite (He) with
high reducibility on the inside.
[0020] Note that layer 2 may be a mixed layer of limestone-based raw material and solid
fuel-based raw material, or a lamination of a limestone-based raw material layer (inside)
and a solid fuel-based raw material layer (outside). In either case, limestone contents
in layer 2 allow calcium ferrite (CF) with high strength to be formed on the surface
of the sintered ore.
[0021] In this respect, it is important for the iron ore raw material of core 1 to contain
iron ore having an alkali metal content of 0.05 mass% or more (also referred to hereinafter
as "high-alkaline iron ore"). In other words, by containing high-alkaline iron ore
in the iron ore raw material of core 1, a catalytic effect can be obtained via an
alkali metal, and close arrangement of calcium ferrite can be achieved, thereby further
improving reducibility of sintered ore. It is difficult to obtain the above effect
if the alkali metal content of the high-alkaline iron ore is less than 0.05 mass%.
[0022] It is preferred, however, that the alkali metal content of the high-alkaline iron
ore having an alkali metal content of 0.05 mass% or more is 0.30 mass% or less. The
reason is that if the alkali metal content is excessively high, the proportion of
the alkali metal obtained in the sintering machine increases even when the mix proportion
is small, and the amount of the alkali metal in the blast furnace increases accordingly.
This may cause accumulation of the alkali metal in the furnace, and formation of layers
of alkali metals and adhesion to the furnace wall, thereby disturbing proper blast
furnace operations. The dispersibility of the alkali metal in the sintered ore may
also decrease, thereby reducing the above effect.
[0023] In the iron ore raw material, the mix proportion of the high-alkaline iron ore is
preferably 20 mass% to 60 mass%. The reason is that a mix proportion of less than
20 mass% is less effective for improving reducibility, while a mix proportion of more
than 60 mass% increases the proportion of the alkali metal in the sintered ore obtained
in the sintering machine, which may result in an increase in alkali contents in the
blast furnace, accumulation of the alkali metal in the furnace, and formation of alkali
metal layers and adhesion to the furnace wall, which may adversely affect blast furnace
operations. There is another concern that the reduction-disintegration index of the
sintered ore may excessively increase, thereby deteriorating permeability in the blast
furnace and resulting in an increased coke ratio. The remaining part of the iron ore
raw material other than the high-alkaline iron ore is iron ore having an alkali metal
content of less than 0.05 mass% (also referred to hereinafter as "general iron ore").
Moreover, SiO
2 raw material may optionally be added to the iron ore raw material.
[0024] The iron ore raw material preferably forms core 1 such that the core takes any of
Forms I to III below. In each case, the above action can be provided by the alkali
metal. Each form has the following characteristics.
Form I: Mixed layer of general iron ore and high-alkaline iron ore
[0025] In this Form A, a mixed layer of general iron ore and high-alkaline iron ore enables
an alkali metal to be uniformly dispersed within the sintered ore. As a consequence,
it becomes possible to increase reducibility by increasing the surface area of the
alkali metal which exhibits catalytic action, and by enhancing the catalytic effect.
Additionally, the strength of the sintered ore may also mitigate formation of a brittle
zone, thereby ensuring cold strength.
Form II: Lamination of a first layer formed of general iron ore and a second layer
formed of high-alkaline iron ore covering the surface of the first layer
[0026] In this Form B, an alkali metal which exhibits catalytic action is present on the
surface side of the core. As a consequence, it becomes possible to fully make use
of the catalytic effect of the alkali metal, thereby increasing reducibility.
Form III: Lamination of a first layer formed of high-alkaline iron ore and a second
layer formed of general iron ore covering the surface of the first layer
[0027] In this Form C, high-alkaline iron ore is present inside the core of each quasiparticle
before subjection to sintering, and the proportion of an alkali metal present in the
calcium ferrite phase formed in the surface of the sintered ore is reduced. As a consequence,
reduction disintegration properties can be improved without interfering with the catalytic
action of the alkali metal.
[0028] It is also preferred that the high-alkaline iron ore has a mean particle size of
2 mm or more, and the general iron ore has a mean particle size of less than 2 mm.
As used herein with respect to each iron ore, a mean particle size refers to an arithmetic
mean of the weight ratio and the representative particle size of the iron ore when
classified by particle size using a sieve.
[0029] Specifically, the high-alkaline iron ore preferably has a mean particle size of 2
mm or more for the following reason. During the process of granulating the raw material
to be fed to the sintering machine into quasiparticles, ore having a relatively large
particle size will be unevenly distributed in the center of each quasiparticle, which
fact is advantageous for reducing the proportion of an alkali metal present in the
calcium ferrite phase that is formed in the surface of iron ore after sintering the
quasiparticles. If an alkali metal is contained in large quantities in the calcium
ferrite phase, reduction disintegration properties deteriorate. Thus, setting the
mean particle size of the high-alkaline iron ore to 2 mm or more is advantageous for
producing sintered ore that has a low reduction-disintegration index.
[0030] On the other hand, the general iron ore preferably has a mean particle size of less
than 2 mm for the following reason.
[0031] Specifically, during the process of granulating into quasiparticles, ore having a
small mean particle size will be unevenly distributed on the outside of quasiparticles,
which fact may mitigate incorporation of large amounts of high-alkaline ore and calcium
ferrite phase.
[0032] A method of producing quasiparticles for sintering according to the disclosure will
now be described below.
[0033] Firstly, FIG. 8 illustrates an exemplary granulation flow (process A) for producing
a desirable quasiparticle structure according to the disclosure. In this process A,
the aforementioned high-alkaline iron ore 1a and general iron ore 1b, and optionally
SiO
2-containing raw material 1c are charged from the mixer inlet of a drum mixer 4. Then,
limestone-based raw material 2a and solid fuel-based raw material 2b are added to
the drum mixer 4 from the mixer outlet of the drum mixer 4 and granulated therein,
and quasiparticles for sintering, in the form of Form I above, can be obtained with
limestone-based raw material 2a and solid fuel-based raw material 2b adhered to the
circumference of a core with mixture of the high-alkaline iron ore 1a and the general
iron ore 1b.
[0034] In addition, FIG. 9 illustrates an exemplary granulation flow (process B) for producing
quasiparticles according to the disclosure. In this process B, the following materials
are subjected to pre-granulation using a granulator 3: high-alkaline iron ore and
general iron ore, e.g. high-alkaline iron ore 1a that has an alkali metal content
of approximately 0.05 mass% to 1.0 mass% and a mean particle size of 2 mm or more,
and general iron ore 1b that has an alkali metal content of less than 0.05 mass% and
a mean particle size of less than 2 mm; and, optionally, fine SiO
2-containing raw material 1c (such as iron ore, silica stone, serpentinite, and Ni
slag) that has a SiO
2 content of approximately 0.5 % to 5.0 % and a mean particle size of less than 2 mm,
e.g. approximately 0.1 mm to 1.0 mm. In this pre-granulation, a first layer is formed
by the general iron ore 1b and optionally added SiO
2, and the high-alkaline iron ore 1a is caused to be adhered, as a second layer, to
the circumference of the first layer.
[0035] By changing the order of granulation in the pre-granulation process, the layering
order of the high-alkaline iron ore 1a and the general iron ore 1b can be altered.
That is, opposite to the above, the high-alkaline iron ore 1a and optionally added
SiO
2 may be formed as a first layer, and a second layer may be formed by adhering the
general iron ore 1b to the circumference of the first layer.
[0036] Subsequently, limestone-based raw material 2a alone, or limestone-based raw material
2a and solid fuel-based raw material 2b as heat source (such as coke and anthracite)
are further added to, and mixed and granulated in the drum mixer 4 to thereby obtain
quasiparticles for sintering in Form II or III, as described above, such that limestone-based
raw material 2a and solid fuel-based raw material 2b are adhered to the circumference
of each core of the iron ore raw material that comprises a first layer formed of high-alkaline
iron ore 1a and a second layer formed of general iron ore 1b adhered to the circumference
of the first layer.
[0037] Further, FIG. 10 illustrates an exemplary granulation flow (process C) for producing
another desirable quasiparticle structure according to the disclosure. In this process
C, a plurality of (in this example, two) drum mixers are provided, and the aforementioned
high-alkaline iron ore 1a and general iron ore 1b, and optionally SiO
2-containing raw material 1c are charged from the inlet of the drum mixer 4 and granulated
therein, limestone-based raw material 2a alone, or limestone-based raw material 2a
and solid fuel-based raw material 2b are added from the inlet of the final stage drum
mixer 4' located at the position pointed to by broken arrow, or from the outlet located
at the position pointed to by solid arrow, and granulated. If only limestone-based
raw material 2a is added, solid fuel-based raw material 2b may be added subsequently,
and the limestone-based raw material 2a and the solid fuel-based raw material 2b may
be granulated layer-by-layer. Note that if the limestone-based raw material 2a and
the solid fuel-based raw material 2b have a mean particle size of 0.5 mm or less,
preferably 0.25 mm or less, they can adhere to each other more easily, enabling the
solid fuel-based raw material 2b to cover the surface of the limestone-based raw material
2a.
[0038] According to Process A, B, or C, iron ore raw material including high-alkaline iron
ore may be formed as a core, and limestone-based raw material and solid fuel-based
raw material as heat source may be adhered to the circumference of the core, so that
the resulting quasiparticle can be coated and granulated with more than one layer.
This configuration enables delaying the reaction between CaO and SiO
2 during a sintering process of sintering raw material formed of quasiparticles, mitigating
the formation of calcium silicate (CS) with low cold strength, and causing calcium
ferrite (CF) with high strength to be selectively formed on the surface of the lump
and hematite (He) with high reducibility to be selectively formed on the inside of
the lump. As a result, sintered ore that is rich in fine pores, excellent in reducibility,
and high in cold strength may be stably produced.
EXAMPLES
[0039] Sintering raw materials were formulated as illustrated in Table 2, and quasiparticles
for sintering were granulated by Process A or B in FIG. 8 or 9 according to the disclosure.
The quasiparticles were transported to a Dwight Lloyd sintering machine and charged
on a palette. For comparison, an operation was also conducted in which quasiparticles
were granulated by the process of simultaneously mixing iron ore raw material, SiO
2-containing raw material, limestone-based raw material, and coke powder, and the quasiparticles
were transported to the Dwight Lloyd sintering machine and charged on the palette.
Then sintering was performed on the palette, and measurement was made of the reducibility
(JIS-RI), reduction-disintegration index (RDI), and sintering strength (TI) of the
resulting sintered ore. The measurement results are shown in Table 3.
[0040] The reducibility (JIS-RI) was measured in conformance with JIS M8713. The reduction-disintegration
index (RDI) was measured in accordance with JIS M8720. The sintering strength was
determined by measuring the tumble strength (tumbler strength TI) of sintered ore
products in accordance with JIS M8712.
[Taable 2]
[0041]
Table 2
Formulation |
Unit |
a |
b |
c |
d |
e |
High-alkaline Iron Ore |
mass% |
0 |
20 |
40 |
60 |
80 |
General Iron Ore |
mass% |
85 |
65 |
45 |
25 |
5 |
SiO2-containing Raw Material |
kg/t-sintered ore |
15 |
15 |
15 |
15 |
15 |
Limestone-based Powder Raw Material |
kg/t-sintered ore |
13 |
13 |
13 |
13 |
13 |
Solid Fuel-based Powder Raw Material |
kg/t-sintered ore |
5 |
5 |
5 |
5 |
5 |
Notes:
(1) In the formulation, the total amount of high-alkaline iron ore, genral iron ore,
and SiO2-containing raw material is taken as 100 %, excluding limestone-based raw material
and solid fuel-based raw material.
(2) As the SiO2-containing raw material, limestone-based powder raw material, and solid fuel-based
powder raw material, the following used:
SiO2-containing raw material: silica sand
Limestone-based poweder raw material: limestone, quick lime
Solid fuel-based powder raw material: coke, anthracite |
[Table 3-1]
[0042]
Table 3-1
No |
Formulation |
FormofQuasiparticle |
Alkali Metal Content (mass%) |
Mean Particle Size (mm) |
Carbonaceous Material (kg/t-sintered ore) |
JIS-RI (%) |
RDI (%) |
TI (%) |
Remarks |
High-alkaline Ore |
General Ore |
High-alkaline Ore |
General Ore |
Lime |
Solid Fuel |
|
|
|
|
1 |
a |
Simultaneous Mixing |
- |
0.02 |
- |
1.4 |
(13) |
(5) |
56.5 |
35.2 |
90.2 |
Comparative Example 1 |
2 |
a |
Form I |
- |
0.02 |
- |
1.4 |
13 |
5 |
60.5 |
30.0 |
90.1 |
Comparative Example 2 |
3 |
a |
Simultaneous Mixing |
- |
0.045 |
- |
1.4 |
(13) |
(5) |
58.2 |
38.3 |
90.0 |
Comparative Example 3 |
4 |
a |
Form I |
- |
0.045 |
- |
1.4 |
13 |
5 |
61.1 |
31.4 |
90.1 |
Comparative Example 4 |
5 |
b |
Simultaneous Mixing |
0.1 |
0.02 |
1.4 |
1.4 |
(13) |
(5) |
58.9 |
39.2 |
90.2 |
Comparative Example 5 |
6 |
b |
Form I |
0.1 |
0.02 |
1.4 |
1.4 |
13 |
5 |
65.8 |
33.2 |
90.4 |
Example 1 |
Note: In "Carbonaceous Material Coating," parentheses indicate simultaneous mixing
of lime, solid fuel, and ore (Form of Quasiparticle corresponds to "Simultaneous Mixing"). |
[Table 3-2]
[0043]
Table 3-2
No |
Formulation |
Form of Quasiparticle |
Alkali Metal Content (mass%) |
Mean Particle Size (mm) |
Carbonaceous Material Coating (kg/t-sintered ore) |
JIS-RI (%) |
RDI (%) |
TI (%) |
Remarks |
High-alkaline Ore |
General Ore |
High-alkaline Ore |
General Ore |
Lime |
Solid Fuel |
|
|
|
|
7 |
b |
Form I |
0.12 |
0.02 |
2.5 |
1.4 |
13 |
5 |
65.3 |
32.2 |
89.8 |
Example 2 |
8 |
b |
Form II |
0.12 |
0.02 |
2.5 |
1.4 |
13 |
5 |
63.3 |
33.4 |
89.9 |
Example 3 |
9 |
b |
Form III |
0.12 |
0.02 |
2.5 |
1.4 |
13 |
5 |
66.5 |
32.6 |
90.1 |
Example 4 |
10 |
c |
Form I |
0.12 |
0.02 |
2.5 |
1.4 |
13 |
5 |
66.2 |
30.7 |
90.1 |
Example 5 |
11 |
c |
Form II |
0.12 |
0.02 |
2.5 |
1.4 |
13 |
5 |
64.3 |
31.8 |
90.0 |
Example 6 |
12 |
c |
Form III |
0.12 |
0.02 |
2.5 |
1.4 |
13 |
5 |
67.4 |
31.4 |
90.0 |
Example 7 |
13 |
d |
Form I |
0.12 |
0.02 |
2.5 |
1.4 |
13 |
5 |
65.8 |
31.4 |
90.1 |
Example 8 |
14 |
d |
Form II |
0.12 |
0.02 |
2.5 |
1.4 |
13 |
5 |
63.7 |
32.7 |
89.8 |
Example 9 |
15 |
d |
Form III |
0.12 |
0.02 |
2.5 |
1.4 |
13 |
5 |
66.8 |
32.1 |
89.9 |
Example 10 |
16 |
e |
Form I |
0.3 |
0.02 |
2.5 |
1.4 |
13 |
5 |
65.3 |
40.2 |
90.1 |
Example II |
17 |
e |
Form II |
0.3 |
0.02 |
2.5 |
1.4 |
13 |
5 |
63.3 |
41.7 |
90.1 |
Example 12 |
18 |
e |
Form III |
0.3 |
0.02 |
2.5 |
1.4 |
13 |
5 |
66.2 |
41.4 |
90.1 |
Example 13 |
[Table 3-3]
[0044]
Table 3-3
No |
Formulation |
Form of Quasiparticle |
Alkali Metal Content (mass%) |
Mean Particle Size (mm) |
Carbonaceous Material Coating (kg/t-sintered ore) |
JIS-RI (%) |
RDI (%) |
TI (%) |
Remarks |
High-alkaline Ore |
General Ore |
High-alkalin e Ore |
General Ore |
Lime |
Solid Fuel |
|
|
|
|
19 |
c |
Form III |
0.05 |
0.02 |
2.5 |
1.4 |
13 |
5 |
66.3 |
29.4 |
89.8 |
Example 14 |
20 |
c |
Form III |
0.10 |
0.02 |
2.5 |
1.4 |
13 |
5 |
67.1 |
31.1 |
90.0 |
Example 15 |
21 |
c |
Form III |
0.15 |
0.02 |
2.5 |
1.4 |
13 |
5 |
67.7 |
32.0 |
89.8 |
Example 16 |
22 |
c |
Form III |
0.30 |
0.02 |
2.5 |
1.4 |
13 |
5 |
69.6 |
33.4 |
90.1 |
Example 17 |
23 |
c |
Form III |
0.35 |
0.02 |
2.5 |
1.4 |
13 |
5 |
69.2 |
38.4 |
89.8 |
Example 18 |
24 |
c |
Form III |
0.12 |
0.02 |
0.5 |
1.0 |
13 |
5 |
62.3 |
34.9 |
89.8 |
Example 19 |
25 |
c |
Form III |
0.12 |
0.02 |
1.0 |
1.0 |
13 |
5 |
62.6 |
34.8 |
89.9 |
Example 20 |
26 |
c |
Form III |
0.12 |
0.02 |
1.5 |
1.0 |
13 |
5 |
62.7 |
34.7 |
89.8 |
Example 21 |
27 |
c |
Form III |
0.12 |
0.02 |
2.0 |
1.0 |
13 |
5 |
63.5 |
33.3 |
89.9 |
Example 22 |
28 |
c |
Form III |
0.12 |
0.02 |
2.5 |
1.0 |
13 |
5 |
64.5 |
31.6 |
90.0 |
Example 23 |
[0045] It can be seen from Table 3 that Nos. 6 to 28, in which limestone-based raw material
and coke powder were coated on the circumference of each core formed of iron ore raw
material according to the present disclosure, were all improved in reducibility (JIS-RI)
over Nos. 1, 3, and 5, in which iron ore raw material, SiO
2-containing raw material, limestone-based raw material, and coke powder were mixed
simultaneously. Moreover, Nos. 6 to 28 differ from Nos. 2 and 4, in which limestone-based
raw material and coke powder were also coated on the circumference of each core formed
of iron ore raw material, in that Nos. 6 to 28 contained high-alkaline iron ore in
each core formed of the iron ore raw material. This difference contributes to improved
reducibility.
1. A quasiparticle for sintering comprising, at least, iron ore raw material, limestone-based
raw material, and solid fuel-based raw material, each being used to produce sintered
ore for blast furnaces,
wherein the iron ore raw material forms a core of the quasiparticle, and the limestone-based
raw material and the solid fuel-based raw material are coated on the circumference
of the core, and
wherein the core formed of the iron ore raw material contains high-alkaline iron ore
having an alkali metal content of 0.05 mass% or more.
2. The quasiparticle for sintering according to claim 1, wherein the core formed of the
iron ore raw material comprises:
a first layer that is formed of general iron ore having an alkali metal content of
less than 0.05 mass%; and
a second layer that is formed of the high-alkaline iron ore having an alkali metal
content of 0.05 mass% or more and that covers the surface of the first layer.
3. The quasiparticle for sintering according to claim 1, wherein the core formed of the
iron ore raw material comprises:
a first layer that is formed of the high-alkaline iron ore having an alkali metal
content of 0.05 mass% or more; and
a second layer that is formed of the general iron ore having an alkali metal content
of less than 0.05 mass% and that covers the surface of the first layer.
4. The quasiparticle for sintering according to any one of claims 1 to 3, wherein the
iron ore raw material contains the high-alkaline iron ore having an alkali metal content
of 0.05 mass% or more in an amount of 20 mass% or more.
5. The quasiparticle for sintering according to any one of claims 1 to 4, wherein the
high-alkaline iron ore having an alkali metal content of 0.05 mass% or more has a
mean particle size of 2 mm or more, and the general iron ore having an alkali metal
content of less than 0.05 mass% has a mean particle size of less than 2 mm.
6. The quasiparticle for sintering according to any one of claims 1 to 5, wherein the
alkali metal content of the high-alkaline iron ore having an alkali metal content
of 0.05 mass% or more is 0.30 mass% or less.
7. The quasiparticle for sintering according to any one of claims 1 to 6, wherein the
limestone-based raw material and the solid fuel-based raw material are coated layer-by-layer
on the circumference of the core.
8. The quasiparticle for sintering according to any one of claims 1 to 7, wherein a mixed
layer of the limestone-based raw material and the solid fuel-based raw material is
coated on the circumference of the core.
9. A method of producing a quasiparticle for sintering, the method comprising:
when mixing and granulating, at least, iron ore raw material, limestone-based raw
material, and solid fuel-based raw material, each being used to produce sintered ore
for blast furnaces,
mixing and granulating the iron ore raw material containing high-alkaline iron ore
having an alkali metal content of 0.05 mass% or more to obtain a granulated particle;
and
causing the limestone-based raw material and the solid fuel-based raw material to
be adhered to the granulated particle and, subsequently, performing granulation.
10. A method of producing a quasiparticle for sintering, the method comprising:
when mixing and granulating, at least, iron ore raw material, limestone-based raw
material, and solid fuel-based raw material, each being used to produce sintered ore
for blast furnaces,
mixing and granulating general iron ore having an alkali metal content of less than
0.05 mass% and SiO2-containing raw material to form a first layer;
causing high-alkaline iron ore having an alkali metal content of 0.05 mass% or more
to be adhered to the surface of the first layer, and subsequently performing granulation
to form a second layer; and
causing the limestone-based raw material and the solid fuel-based raw material to
be adhered to the surface of the second layer and, subsequently, performing granulation.
11. A method of producing a quasiparticle for sintering, the method comprising:
when mixing and granulating, at least, iron ore raw material, limestone-based raw
material, and solid fuel-based raw material, each being used to produce sintered ore
for blast furnaces,
mixing and granulating high-alkaline iron ore having an alkali metal content of 0.05
mass% or more to form a first layer;
causing general iron ore having an alkali metal content of less than 0.05 mass% to
be adhered to the surface of the first layer, and subsequently performing granulation
to form a second layer; and
causing the limestone-based raw material and the solid fuel-based raw material to
be adhered to the surface of the second layer and, subsequently, performing granulation.
12. The method of producing a quasiparticle for sintering according to any one of claims
7 to 11, wherein the high-alkaline iron ore having an alkali metal content of 0.05
mass% or more has a mean particle size of 2 mm or more, and the general iron ore having
an alkali metal content of less than 0.05 mass% has a mean particle size of less than
2 mm.
13. The method of producing a quasiparticle for sintering according to any one of claims
7 to 12, wherein mixed powder of the limestone-based raw material and the solid fuel-based
raw material is adhered and, subsequently, granulation is performed.
14. The method of producing a quasiparticle for sintering according to any one of claims
7 to 12, wherein after the adhering of the limestone-based raw material, the solid
fuel-based raw material is adhered to an outer surface of a layer of the limestone-based
raw material and, subsequently, granulation is performed.