Technical Field
[0001] The present invention relates to fired pellets for reduction that can be effectively
used in a solid reduction furnace, and a method for producing the same.
Background Art
[0002] In recent years, various technologies have been developed to reduce CO
2 emissions in order to avoid global warming due to an increase in the CO
2.
[0003] Under such a circumstance, also in the field of the iron making industry, an ironmaking
method performed with a solid reduction furnace, which is a hydrogen-based reduction
process, has been gaining attention, and studies have been made on fired pellets used
for such a method. Incidentally, it is known that a raw material (fired pellets) fed
into the furnace, when passing through a high-temperature zone in such a solid reduction
furnace, causes a degradation phenomenon accompanied by volume expansion as the hematite
phase in the fired is reduced and transformed into magnetite phases. It is also known
to cause contact and fusion between metallic irons and between low-melting-temperature
slags. This results in clustering in the furnace, or a hanging phenomenon such that
the pellets in the furnace become immovable and thus cannot be removed from the bottom
of the furnace. Such clustering is a significant problem to be solved for, in particular,
a solid reduction furnace for performing hydrogen-based reduction.
[0004] Under such a circumstance, there have been proposed several prior arts for preventing
the clustering observed in a solid reduction furnace as described above. For example,
Patent Literature 1 proposes a method for covering the surfaces of pellets with, for
example, Ca(OH)
2 or Mg(OH)
2. Patent Literature 2 proposes a method for preventing reduction-degradation and obtaining
a fired pellet with fewer blisters by covering the surface of sintered agglomerated
ore (pellet) with a powdery solid fuel. Patent Literature 3 is directed to prevent
the occurrence of clustering in a solid reduction furnace as well as reduce heat loss
and improve the operation efficiency by covering the surface of a fired pellet with
iron ore mixed with cement. Further, Patent Literature 4 proposes a method for performing
covering with a material containing a calcium-iron compound represented by CaxFeyOz
(1<y/x≤2; 1≤z).
Citation List
Patent Literature
Summary of Invention
Technical Problem
[0006] Each of the above conventional methods (Patent Literatures 1 to 4) is a method for
reducing the contact between metallic irons after reduction, which can cause clustering
observed around a high-temperature zone (500 to 600°C) in a solid reduction furnace,
such as a shaft furnace, by mainly interposing non-metallic components therebetween.
However, according to the inventors' research, such clustering prevention methods
of the conventional technologies are insufficient. These methods have a problem in
that it also requires to adapt a covering step of non-metallic components, which increases
the cost, and the addition of a dedicated facility.
[0007] Accordingly, an object of the present invention is to propose, in producing fired
pellets for use in a solid reduction furnace, fired pellets that is effective in preventing
clustering by reducing the possibility of contact between low-melting-temperature
slags and thus preventing the fusion between the slags, and a method for producing
such fired pellets.
Solution to Problem
[0008] The present invention relates to a method that can solve the above problems of the
conventional technologies and has been developed to achieve the above object. First,
the present invention proposes fired pellets for reduction characterized in that a
ratio of high-viscosity slag components (Al
2O
3+MgO+SiO
2) to total Fe (T.Fe) satisfies the following Expression (1):
where Al2O3 represents a concentration (mass%) of Al2O3 in the fired pellets,
MgO represents a concentration (mass%) of MgO in the fired pellet,
SiO2 represents a concentration (mass%) of SiO2 in the fired pellets, and
T.Fe represents a concentration (mass%) of T.Fe in the fired pellets.
[0009] Second, the present invention proposes a method for producing the above fired pellets
for reduction, comprising performing reduction and firing by using an iron-containing
raw material formulated to achieve an average LOI (Loss on Ignition) of 5% or more.
[0010] Note that the fired pellets for reduction of the present invention may include the
following feature that is considered to be able to provide a more preferable embodiment.
- (a) A proportion of high-viscosity slag components (Al2O3+MgO+SiO2) to total Fe (T.Fe) satisfies the following Expression (2):

where Al2O3 represents a concentration (mass%) of Al2O3 in the fired pellets,
MgO represents a concentration (mass%) of MgO in the fired pellets,
SiO2 represents a concentration (mass%) of SiO2 in the fired pellets, and
T.Fe represents a concentration (mass%) of T.Fe in the fired pellets.
- (b) The porosity is 20% or more.
- (c) The porosity is 30% or more.
[0011] In addition, the production of the fired pellets for reduction may include the following
feature that is considered to be able to provide a more preferable embodiment.
(d) The iron-containing raw material has been subjected to a crystal water removal
pretreatment in advance so as to achieve an average LOI (Loss on Ignition) of 2% or
less.
(e) The pretreatment for removal of crystal water involves heating and drying using
a rotary kiln and using a measurement value of a sample at the exit side of the kiln
as the average LOI (Loss on Ignition) of the iron-containing raw material.
(f) A mixed raw material containing 4 mass% to 24 mass% M.Fe is prepared by mixing
a raw material containing M.Fe, and the mixed raw material is granulated and fired.
(g) The raw material is reduced iron having a particle size of 3 mm or less that has
been reduced in a solid reduction furnace.
(h) The reduced iron contains 78 mass% or more M.Fe. M.Fe hereinafter refers to metallic
iron.
Advantageous Effects of Invention
[0012] The fired pellets for reduction of the present invention according to the above-described
configuration contain high-viscosity slag components (Al
2O
3, MgO, and SiO
2) at a high proportion relative to the total iron can reduce the generation of low-melting-temperature
slag due to FeO during reduction in a solid reduction furnace and its fluidity. Consequently,
it is possible to prevent the possibility of contact or fusion between the pellets
due to such interposed slag and thus effectively prevent the above-described clustering
in the reduction furnace that is a problem to be solved.
[0013] In addition, the production method according to the present invention involves the
use of a high-LOI raw material formulated as an iron-containing raw material, causing
the obtained fired pellets to be porous. Thus, the possibility of contact between
the metallic irons is reduced, thereby effectively preventing clustering and increasing
the operation efficiency of a solid reduction furnace.
Brief Description of Drawing
[0014] [Fig. 1] Fig. 1 is a graph illustrating the relationship between (Al
2O
3+MgO+SiO
2)/T.Fe and LOI of Australian iron ore that is an iron-containing raw material to be
mixed.
Description of Embodiments
[0015] A solid reduction furnace used in the present invention is a furnace for reducing
fed fired pellets for reduction to Fe having a reduction degree of 90% or more by
using a hydrogen gas, etc., as a reducing gas. In the operation of such a solid reduction
furnace, the properties of raw material fed into the furnace, that is, the fired pellets
are important.
[0016] What is most important for the fired pellets is whether the pellets can be prevented
from contacting or fusing with each other, which would otherwise result in clustering,
in a high-temperature zone (500 to 800°C) of the solid reduction furnace as described
above. In response to such demand, in the present invention, studies have been made
on the relationship between an iron-containing raw material such as metallic iron,
iron oxide such as iron ore, iron sulfide, or ironmaking dust and high-viscosity slag
components. As a result, from the viewpoint of the fluidity of the various raw materials
in the furnace, it is found preferable to appropriately manage the relationship particularly
between the iron-containing raw material and high-viscosity slag components. That
is, the high-viscosity slag is always controlled to be generated in the furnace so
that an undesirable flow in the high-temperature zone is suppressed. This can prevent
the fusion between slags, thereby preventing clustering.
[0017] As described previously, in the present invention, it has been found to be effective
to include the high-viscosity slag components in a given ratio in an iron-containing
raw material, iron ore, or an auxiliary material to be mixed.
[0018] As the components that can be the high-viscosity slag, focus is placed on (Al
2O
3, MgO, and SiO
2), in particular. When the total content of such components is maintained at a predetermined
ratio relative to the total iron
[0019] (T.Fe), it becomes possible to effectively prevent the slag-to-slag fusion caused
in the furnace.
[0020] This can be achieved when the fired pellets for reduction have a component composition
such that the high-viscosity slag components (Al
2O
3+MgO+SiO
2) are contained in a given ratio relative to the total iron (T.Fe) in the iron-containing
raw material. That is, when the fired pellets satisfy the relationship of Expression
(1) below.

[0021] In Expression (1) above, Al
2O
3 represents the concentration (mass%) of Al
2O
3 in the fired pellets for reduction. MgO represents the concentration (mass%) of MgO
in the fired pellets for reduction. SiO
2 represents the concentration (mass%) of SiO
2 in the fired pellets for reduction. T.Fe represents the total Fe concentration (mass%)
in the fired pellets for reduction.
[0022] In the present invention, there exists a more preferable relationship between the
high-viscosity slag components (Al
2O
3+MgO+SiO
2) and the total iron (T.Fe) from the viewpoint of preventing the contact or fusion
between the slags in the high-temperature range of the furnace, which is Expression
(2) below. The relationship indicates that the high-viscosity slag components are
contained in a higher amount.

[0023] In Expression (2) above, Al
2O
3 represents the concentration (mass%) of Al
2O
3 in the fired pellets for reduction. MgO represents the concentration (mass%) of MgO
in thefired pellets for reduction. SiO
2 represents the concentration (mass%) of SiO
2 in the fired pellets for reduction. T.Fe represents the total Fe concentration (mass%)
in the fired pellets for reduction.
[0024] Note that in the present invention, the total Fe in the iron-containing raw material
refers to the total value of the iron concentrations including the concentrations
of metallic iron (M.Fe) and iron compounds (iron oxide, iron sulfide, calcium ferrite,
etc.). Meanwhile, the high-viscosity slag components refer to the total value of the
concentrations of Al
2O
3, MgO, and SiO
2 contained in the iron-containing raw material, such as iron ore or ironmaking dust;
an auxiliary material (limestone, quicklime, dolomite, etc.); and a binder (bentonite,
etc.).
[0025] The Al
2O
3, MgO, and SiO
2 concentrations can be determined as follows. First, the Al concentration, Mg concentration,
and Si concentration are measured by elemental analysis such as fluorescent X-ray
analysis, for example. Then, each oxide concentration can be determined by multiplying
the element concentration thus determined by (the molecular weight of the oxide per
element/atomic weight). Specifically, for example, the Al
2O
3 concentration can be determined by multiplying the Al concentration measured by elemental
analysis, such as fluorescent X-ray analysis, by (the Al
2O
3 molecular weight/2)/the Al atomic weight = 50.98/26.98 = 1.890.
[0026] It is also critical to control the porosity of the fired pellets for reduction according
to the present invention, That is, when the fired pellets for reduction are made porous
(20% or more, preferably 30% or more), the number of contact points between the pellets
can be reduced, which can also reduce the contact between metallic irons and prevent
fusion, thereby contributing to the prevention of the clustering described above.
In this respect, a porosity of less than 20% is not effective in preventing fusion.
The upper limit is approximately 60% from the viewpoint of strength.
[0027] Next, the method for producing the fired pellets according to the present invention
will be described. When producing the fired pellets for reduction according to the
present invention, in order for the fired pellets to satisfy the above relationship
between the high-viscosity slag components (Al
2O
3+MgO+SiO
2) and the total iron (T.Fe), for example, it is possible to use an iron ore originally
having a composition of components satisfying the above relationship, or to selectively
use and mix a plurality of iron ores to satisfy the above relationship. For example,
one or more of iron ores (brands) shown in Fig. 1, which are Australian iron ores,
may be mixed, followed by granulation with a binder, such as bentonite, and an auxiliary
material, such as quicklime, added thereto as appropriate.
[0028] When feeding the above fired pellets into the solid reduction furnace and reducing
the pellets therein it is critical that these pellets do not have properties that
would cause clustering in a high-temperature reducing atmosphere in the furnace. Therefore,
in the present invention, focus is placed particularly on LOI (Loss on Ignition),
the appropriate value of which has been studied. That is, in the production method
according to the present invention, some of the types of iron ore (A to Z) shown in
Fig. 1 are selectively used (mixed) to achieve a LOI (Loss on Ignition) value of 5%
or more so that LOI≥5% is satisfied, thereby reducing clustering more effectively.
This is because when volatile components, such as crystal water, in the pellets are
dissociated and vaporized in the firing process for pellets, and then dissipate to
the outside of the pellets, the volume of the mineral phases remaining in the pellets
is reduced, resulting in voids between the adjacent mineral phases.
[0029] Next, in the production method according to the present invention, for the iron-containing
raw material to achieve the relation LOI ≥ 5%, it is preferable to apply a pretreatment
such as a process for removing crystal water to the iron ore to be used in advance
so as to achieve LOI ≤ 2%. Since many iron-containing raw materials such as raw material
iron ore have a high crystal water content, pellets often burst during granulation
due to water vapor generated from the crystal water. Thus, it would be unavoidable
to increase the temperature slowly. This would reduce productivity.
[0030] In the pretreatment such as a process for removing crystal water, it is preferable
to use values measured at the exit side of the granulator such as rotary kiln for
LOI evaluation.
[Examples]
<Embodiment 1>
[0031] The Examples (including Comparative Examples) show how the relationship between T.Fe
and high-viscosity slag components (Al
2O
3+MgO+SiO
2) in fired pellets for reduction affects the clustering in a solid reduction furnace.
[0032] As the iron-containing raw material, i.e. iron ore used herein, mainly one or more
types of Australian iron ores (A to Z) shown in Fig.1 were mixed with an auxiliary
material and reagent (e.g., commercially available Al
2O
3 reagent) as appropriate. Table 1 shows examples of the component compositions of
the mixtures.
[0033] All raw materials including one or more types of the Australian raw materials described
above (exemplified in Fig. 1) (A to Z) were ground in a ball mill and then granulated
with a pelletizer while adding water to achieve a size of 9 to 16 mm. Then, the pellets
after granulation were placed in a dryer to perform drying treatment at 110 °C for
24hr. The pellets were then fed into an electric furnace to be heated at 7 °C/min.,
held at 1250 °C for 10hr, and then cooled at 7 °C/min. Each of the fired pellets obtained,
shown in Table 1, was evaluated using a porosity and a clustering index.
(Clustering evaluation test)
[0034] A sample weighing 500g was fed into a vertical cylindrical furnace with a diameter
ϕ of 100 mm and heated to 1000°C in an N
2 atmosphere. When the temperature of the sample reached 1000°C, a reducing gas was
introduced into the furnace at a rate of 24 NL/min. The composition of the reducing
gas was set to a volume ratio of H
2:N
2=20:80. The sample was then loaded at a rate of 1 kg/cm
2 and held in this state for three hours, followed by cooling in an N
2 atmosphere, so that reduced iron was produced. The reduced iron obtained was then
sieved through a 16 mm sieve mesh, which is the maximum size of a single fired pellet,
to measure the weight Wa (g) of the fired pellets remaining on the sieve. The fired
pellets remaining on the sieve were put into a cylindrical shape vessel (132 mmϕ ×
700 mmL) of an I-type testing machine and were rotated at a rotational speed of 30
rpm for five minutes, to measure the weight Wb (g) of the fired pellets remaining
on the sieve mesh of 16 mm. The fired pellets were evaluated based on a clustering
index that is proportional to the non-crushing clustering proportion Wb/Wa.
(Porosity)
[0035] The porosity of the fired pellets was evaluated by measuring the apparent density
of the pellets and then measuring the real density of the pellets. As shown in Table
1, it is confirmed that each of the fired pellets of Examples 1 to 5 in which (Al
2O
3+MgO+SiO
2)/T.Fe is 0.09 or more has a clustering index of less than 7, and thus has excellent
properties.
[Table 1]
|
LOI (%) of Iron Ore Before Firing |
(Al2O3+MgO+SiO2) /T.Fe |
Porosity (vol%) |
Clustering Index |
Comparative Example 1 |
0.3 |
0.03 |
13 |
52 |
Comparative Example 2 |
0.4 |
0.07 |
8 |
25 |
Example 1 |
5.1 |
0.09 |
22 |
7 |
Example 2 |
7.2 |
0.12 |
20 |
0 |
Example 3 |
8.8 |
0.18 |
23 |
0 |
Example 4 |
9.1 |
0.09 |
33 |
0 |
Example 5 |
10.3 |
0.09 |
49 |
0 |
[0036] Note that Table 2 below shows the component compositions of the fired pellets obtained
in Examples 1 and 2 of Table 1.
[Table 2]
(mass%) |
|
T.Fe |
FeO |
SiO2 |
CaO |
Al2O3 |
MgO |
C/S |
Example 1 |
64.9 |
0.2 |
3.1 |
1.2 |
2.7 |
0.2 |
0.4 |
Example 2 |
62.5 |
0.4 |
4.9 |
2.9 |
2.3 |
0.3 |
0.6 |
<Embodiment 2>
[0037] Next, an evaluation test was conducted to determine whether granulation and firing
can be achieved without breakage during granulation, by subjecting the sample in Example
5, shown in Table 1, to a crystal water removal pretreatment. It should be noted that
the heating rate was set at 200°C/min.
[0038] The result shows that breakage would be caused, when, for example, a number of pores
remains in the ores with crystal water removed, rather than when crystal water was
removed by the crystal water removal treatment. Meanwhile, breakage would not be caused
when the crystal water removal treatment was sufficiently completed, and furthermore,
as long as the LOI of the ore before the treatment was sufficiently high, it is possible
to produce good quality pellets even if the LOI of the ore after the crystal water
removal treatment was low.
[Table 3]
|
LOI (%) of Iron Ore After Crystal Water Removal Treatment |
Results |
Porosity (%) |
Comparative Example 3 |
10.3 |
Breakage |
- |
Comparative Example 4 |
5.2 |
Breakage |
- |
Example 6 |
2 |
Satisfactory |
45 |
Example 7 |
0.7 |
Satisfactory |
43 |
<Embodiment 3>
[0039] Reduced iron (a sample when Wa was measured) obtained by the same method as the method
of Comparative Example 2 in Embodiment 1 (clustering evaluation test) was ground into
particles with a size of 3 mm or less. The resulting particles were mixed with the
unfired raw material of Comparative Example 2. The mixture was used to produce fired
pellets by the method of Embodiment 1. The crushing strength of the resulting fired
pellets was then measured. The measurement results are shown in Table 4.
[0040] In Table 4, "M.Fe" is derived from metallic iron (M.Fe) contained in the reduced
iron. In Examples 10 to 12, reduced iron containing M.Fe = 78 mass% was used. In Example
13, reduced iron containing M.Fe = 80 mass% was used. As a result, it was found that
mixing M.Fe with the raw material can increase the strength of the resulting pellets.
Since clustering is promoted as the amount of powder increases, it is possible to
suppress clustering by increasing the strength of the fired pellets. The reason why
mixing M.Fe with the raw material can increase the strength of the resulting fired
pellets is considered that reduced iron powder is oxidized and generates heat when
the pellet is fired, thus promoting fusion between adjacent particles.
[Table 4]
|
M.Fe (mass%) |
(Al2O3+MgO+SiO2)/T.Fe |
Pellet Strength (kgf) |
Comparative Example 2 |
0 |
0.07 |
178 |
Example 10 |
4 |
0.07 |
218 |
Example 11 |
8 |
0.07 |
221 |
Example 12 |
24 |
0.07 |
233 |
Example 13 |
8 |
0.09 |
255 |
[0041] In this specification, the unit "L" of volume represents 10
-3 m
3. Symbol "N" added to the unit of the volume of a gas represents the volume of the
gas in the standard state, that is, at a temperature of 0°C and a pressure of 101325
Pa. The unit "rpm" of a rotational speed represents the number of rotations per min.
Industrial Applicability
[0042] The fired pellets for solid reduction according to the present invention are the
method that has been developed to be mainly applied to a hydrogen-based direct reduction
process, for example. However, as a matter of course, such fired pellets can also
be used as a raw material for use in a blast furnace, etc.
1. Fired pellets for reduction,
characterized in that
a proportion of high-viscosity slag components (Al2O3+MgO+SiO2) to total Fe (T.Fe) satisfies the following Expression (1):

where Al2O3 represents a concentration (mass%) of Al2O3 in the fired pellets,
MgO represents a concentration (mass%) of MgO in the fired pellets,
SiO2 represents a concentration (mass%) of SiO2 in the fired pellets, and
T.Fe represents a concentration (mass%) of T.Fe in the fired pellets.
2. Fired pellets for reduction,
characterized in that
a proportion of high-viscosity slag components (Al2O3+MgO+SiO2) to total Fe (T.Fe) satisfies the following Expression (2):

where Al2O3 represents a concentration (mass%) of Al2O3 in the fired pellets,
MgO represents a concentration (mass%) of MgO in the fired pellets,
SiO2 represents a concentration (mass%) of SiO2 in the fired pellets, and
T.Fe represents a concentration (mass%) of T.Fe in the fired pellets.
3. The fired pellets for reduction according to claim 1 or 2,
wherein a porosity is 20% or more.
4. The fired pellets for reduction according to any of claims 1 to 3,
wherein a porosity is 30% or more.
5. A method for producing the fired pellets for reduction according to any of claims
1 to 4, wherein
reduction and firing are performed by using an iron-containing raw material formulated
to achieve an average LOI (Loss on Ignition) of 5% or more.
6. The method for producing the fired pellets for reduction according to claim 5, wherein
the iron-containing raw material has been subjected to a crystal water removal pretreatment
in advance so as to achieve an average LOI (Loss on Ignition) of 2% or less.
7. The method for producing the fired pellets for reduction according to claim 5 or 6,
wherein
the crystal water removal pretreatment comprises heating and drying using a rotary
kiln and using a measurement value of a sample at the exit side of the kiln as the
average LOI (Loss on Ignition) of the iron-containing raw material.
8. A method for producing fired pellets for reduction, characterized in that
a mixed raw material containing 4 mass% to 24 mass% M.Fe is prepared by mixing a raw
material containing M.Fe, and the mixed raw material is granulated and fired.
9. The method for producing fired pellets for reduction according to claim 8, wherein
the raw material is reduced iron having a particle size of 3 mm or less that has been
reduced in a solid reduction furnace.
10. The method for producing fired pellets for reduction according to claim 9, wherein
the reduced iron contains 78 mass% or more M.Fe.