[0001] The present invention relates to methods for manufacturing reduced metals by reducing
metal oxides by heating. In particular, the present invention relates to an operation
method of a moving hearth furnace which is used for manufacturing a reduced metal
by reducing a metal oxide by heating.
[0002] Hitherto, various methods for obtaining reduced metals by reducing metal oxides such
as iron ores, steel mill waste, and nickel oxides have been proposed. For example,
a shaft-furnace method represented by Midrex method is known as a manufacturing method
of reduced iron by directly reducing an iron oxide source such as an iron ore or an
iron oxide by using a carbonaceous material or a reducing gas. By this method, metallic
iron is obtained by reducing an iron oxide by using a reducing gas which is manufactured
from natural gas or the like. However, since the reducing gas reformed from natural
gas or the like is used as a reducing agent, the cost of the gas significantly affects
the cost of the final product, and the reduction of the cost is difficult.
[0003] A smelting reduction method such as a DIOS method is known as another method for
obtaining reduced iron by directly reducing iron oxide. However, this method requires
complex operations and is lack of versatility with respect to the productivity and
the equipment cost.
[0004] The inventors paid attention to the above-described circumstances and proposed a
method for manufacturing reduced iron by using a rotary-hearth furnace, which is a
type of moving hearth furnace, by reducing an agglomerate which includes a carbonaceous
reducing agent and an iron oxide (hereinafter referred to as "iron oxide pellet including
carbonaceous reducing agent" or simply as "pellet") (for example, in Japanese Unexamined
Patent Application Publication No. 11-61216). By this method, the carbonaceous material,
which is necessary for reduction, is incorporated with pellets, and another carbonaceous
material is applied to the surfaces of the pellets in order to suppress re-oxidation
at the surfaces of the reduced pellets, whereby the ash content of the carbonaceous
material included in the reduced pellets is reduced, thereby elevating the quality
level of the reduced iron.
[0005] In this method for manufacturing reduced iron by using a moving hearth furnace, the
metal oxide pellet including carbonaceous reducing agents are loaded onto the hearth
of a moving hearth furnace, the pellets are heated mainly with heat of combustion
of burners and the radiant heat from furnace walls, and the iron oxide is reduced
by the incorporated carbonaceous material. That is, the pellets must be supplied with
heat from the outside, because the reduction reaction is an endothermic reaction,
when the iron oxide included in the pellets including carbonaceous reducing agent
is reduced by the carbonaceous material included in the pellets. Therefore, heavy
oil, natural gas, pulverized coal, and/or the like has been hitherto used as a fuel
for the burners and an auxiliary fuel. However, there is a limit to the amount of
production of the above fuels, and in particular, heavy oil and natural gas are comparatively
expensive; therefore, reduction of the manufacturing cost has been difficult.
[0006] The inventors have studied to develop technologies in which metallic iron having
high iron purity can be obtained efficiently in a simple process from iron oxides
having high iron-contents as a matter of course and also from iron ores and the like
which have relatively a low iron-content. As a result, the inventors developed a method
described below and proposed the same in, for example, Japanese Unexamined Patent
Application Publication No. 9-256017.
[0007] The method is characterized in that when metallic iron is manufactured by reducing
metal oxide pellet including carbonaceous reducing agents by heating, an outer skin
of the metallic iron is formed and developed by reducing an iron oxide in a solid
phase, the solid-phase reduction is advanced until the inside iron oxide substantially
disappears, heating continues such that slag flows to the outside of the outer skin
of the metallic iron, and the metallic iron and the slag are separated from each other.
The high-purity metallic iron obtained by this method and the produced slag are solidified
by cooling, the solidified slag is crushed, and the granulated metallic iron is separated
from the slag by magnetic separation or by using a screen, or the metallic iron and
the slag are melted by being heated and are separated from each other by using the
difference of specific gravities. Through these processes, metallic iron having high
iron-purity of 95% or more, or 98% or more is obtainable.
[0008] In the viewpoint of effective use of limited resources, a technology for using combustible
waste materials such as waste oil and waste plastics as fuel for blast furnaces and
converters has been also proposed. However, the combustible waste materials are most
likely to include chlorides or sulfides which form HCl or SO
x as a source of air pollution. Additional facilities are required for disposing of
the source of air pollution included in the exhaust gas; therefore, it has been difficult
to efficiently use the combustible waste materials.
[0009] In processes in which reduced iron is obtained by reducing metal oxides such as iron
ores, steel mill waste, or nickel oxides, an exhaust gas which includes acid such
as HCl and SO
x deriving from chlorides and sulfides included in the source ores and the like is
discharged, the exhaust gas causing environmental pollution. Therefore, various technologies
for resolving this problem have been proposed.
[0010] For example, in Japanese Unexamined Patent Application Publication No. 2001-32024,
a problem in the reduction of a metallic oxide using a rotary-hearth furnace is pointed
out in that relatively a large amount of sulfur is brought onto the rotary hearth
because coal, coke, or oil coke as a reducing agent and heavy oil as an auxiliary
fuel, which contain sulfur, are generally used, thereby increasing sulfur concentration
in the exhaust gas. In order to overcome this problem, a technology for desulfurizing
the exhaust gas has been proposed, in that the amount of an alkali metal to be supplied
together with the raw material is set to be not smaller than twice the amount of the
chemical equivalent which reacts to a sulfur oxide to be released into the exhaust
gas. However, although the sulfur concentration in the exhaust gas can be reduced
by this technology, the harmful components of the exhaust gas other than sulfur (in
particular, chlorine, dioxin, and the like which derive from the chlorides contained
in the raw material) are not considered, and such a problem is left to be solved.
[0011] Accordingly, an object of the present invention is to provide an operation method
of a moving hearth furnace, by which effective utilization of resources can be advanced
and the cost can be reduced by using industrial wastes as a fuel for the moving hearth
furnace for reducing metal oxides. Another object of the present invention is to provide
an operation method of a moving hearth furnace, by which air-pollution problems can
be overcome.
[0012] To these ends, according to the present invention, an operation method of a moving
hearth furnace, in which a reduced metal is obtained by loading a metal oxide into
the moving hearth furnace and reducing the metal oxide by heating, comprises the steps
of supplying a fuel including combustible wastes as a heat source into the moving
hearth furnace and burning the fuel.
[0013] According to the present invention, the type of the fuel including combustible wastes
and the way of supply of the fuel as a heat source into a moving hearth furnace may
be one selected from or may be an appropriate combination of those described below.
(1) A liquid is used as the fuel, and one part of the fuel or the entire fuel is sprayed
into the moving hearth furnace.
(2) A liquid is used as the fuel, and one part of the fuel or the entire fuel is poured
into the moving hearth furnace.
(3) One part of the fuel or the entire fuel is mixed with the metal oxide, and the
mixture is loaded into the moving hearth furnace.
[0014] In the above-described method (1), the diameter of each orifice of a spray for spraying
the fuel is preferably set to be not smaller than 1.1 mm, the temperature in the furnace
is preferably set to be not lower than 150°C, and the fuel is preferably ignited by
a pilot burner which is disposed in the vicinity of a position at which the fuel is
sprayed, whereby stable combustion of the fuel can be maintained.
[0015] In the above-described methods (2) and/or (3), the temperature in the furnace is
preferably set to be not lower than 1100°C and the residence time of the fuel in the
furnace is preferably set to be not shorter than three minutes, whereby a stable operation
can be maintained.
[0016] The operation method of a moving hearth furnace, according to the present invention,
preferably further comprises the step of including an alkali metal to the fuel. The
amount of the alkali metal to be included in the fuel is preferably controlled in
accordance with the amount of S and Cl generated in the furnace during the reduction
by heating.
[0017] According to the present invention, the cost of fuel for reduction by heating can
be significantly reduced by using effectively a fuel including combustible wastes
as a fuel for the reduction by heating of a metal oxide in a moving hearth furnace.
[0018] Fig. 1 is an illustration showing a rotary-hearth furnace and processes of treating
exhaust gas which is discharged from the rotary-hearth furnace, according to the present
invention.
[0019] Fig. 2 is an illustration of the rotary-hearth furnace according to the present invention.
[0020] Fig. 3 is a sectional view along line A-A of the rotary-hearth furnace shown in Fig.
2.
[0021] Fig. 4 is a sectional view of the rotary-hearth furnace shown in Fig. 2 extended
in the longitudinal direction.
[0022] The inventors have studied to overcome the above-described problems from different
angles. As a result, they have found a solution of the above problems in that a reduced
metal having the same quality as that of a known reduced metal can be obtained efficiently
at a low cost by using a fuel including combustible wastes as a heat source which
is necessary to reduce a metal oxide by heating in a moving hearth furnace. The present
invention will be described in detail as follows.
[0023] There are various methods for reducing metal oxides by heating, as described above.
A high-quality reduced metaL could be easily obtained by using the method for reducing
by heating a metal oxide in a moving hearth furnace, which the inventors had proposed.
However, heat must be supplied for the reduction by heating of the metal oxide, and
it was a burner that was generally used as a heat source and that used heavy oil or
natural gas, as a fuel, which are limited resources. Therefore, it is inevitable that
the cost of the fuel continues increasing.
[0024] In contrast, the present invention is characterized in that the cost of fuel is reduced
by using a fuel including combustible wastes as a heat source, thereby effectively
utilizing the wastes as secondary resources, when manufacturing a reduced metal by
reducing a metal oxide by heating in a moving hearth furnace. According to the present
invention, the amount of use of the heavy oil and the natural gas can be reduced,
and dumping of combustible wastes or incineration costs thereof can be suppressed.
[0025] The wastes include industrial wastes, specially controlled industrial wastes, and
domestic wastes. In particular, the industrial wastes and the specially controlled
industrial wastes discharged constantly and in a large volume from particular business
places are conveniently used. The industrial wastes include substances regulated by
"Wastes Disposal and Public Cleaning Law" and an enforcement ordinance thereof, such
as burnt residuals, sludge, waste oil, waste acid, waste alkali, waste plastics, wastepaper,
waste woods, waste textiles, animal and vegetable residuals, waste rubber, waste metals,
waste glass and ceramics, slag, construction and demolition wastes, animal feces and
urine, animal carcasses, and ash dust.
[0026] According to the present invention, combustible wastes among the above industrial
wastes are used as a matter of course, because since a metal oxide is reduced in the
moving hearth furnace, when the fuel includes incombustible wastes, substances which
have not burned remain in the furnace, and the substances are mixed in the reduced
metal, whereby the purity (quality level) of the reduced metal is lowered or complex
operations become necessary for selection of the reduced metal from the substances
which have not burned.
[0027] Therefore, according to the present invention, combustible wastes such as the waste
oil and waste plastics among the above-described wastes are used; one or a mixture
of two or more of these combustible wastes may be used. Among these, the wastes including
waste oil are particularly useful. These wastes having high combustibility and large
combustion energy can also serve to assist the combustion of other wastes which have
relatively low combustibility. When the fuel including the combustible wastes is solid,
the fuel is preferably crushed in a powdered state so that stable burning is maintained.
The fuel including combustible wastes to be used according to the present invention
is most preferably liquid, a typical one being waste oil.
[0028] The type of waste oil is not particularly specified, and waste oil such as waste
mineral oil, waste vegetable oil, and waste animal oil can be used effectively. The
waste oil includes, for example, sludge from oil tanks; sludge of gas oil, kerosene,
gasoline, naphtha, and the like; mineral oil waste of machine oil, lubricant oil,
cutting oil, and the like; oil-press residuals of vegetable oil, such as rapeseed
oil, soybean oil, rice bran oil, cottonseed oil, corn oil, palm oil, and sunflower
seed oil; oil wastes of the above vegetable oil used as materials for food; terpene-based
plant oil wastes such as rosin; and animal oil wastes including animal fat-and-oil
waste liquids of beef, pork, mutton, chicken, fish, and the like. The above-described
types of waste oil may be used independently. However, they are preferably used as
a mixture in an appropriate proportion between several types thereof, thereby maintaining
a stable combustion state.
[0029] In the operation method of a moving hearth furnace according to the present invention,
a liquid fuel including combustible wastes is supplied into the furnace in methods
described below:
<1> A method in which the fuel is sprayed into the moving hearth furnace.
<2> A method in which the fuel is poured into the moving hearth furnace.
<3> A method in which the fuel including combustible wastes is mixed with a metal
oxide and the mixture is supplied into the moving hearth furnace.
[0030] The methods <1> to <3> may be individually used, or a combination of two or more
of the methods <1> to <3> may be used. Preferred embodiments of the above methods
<1> to <3> are described in more detail as follows.
<1> Case of spraying the fuel into the moving hearth furnace
[0031] Since the composition of the fuel including combustible wastes is not always uniform,
and a certain content of moisture is contained in the wastes, the calorific value
is generally instable. However, the fuel can be burned efficiently when being sprayed
by using a spray.
[0032] In this method, the diameter of orifice of the spray for spraying the fuel is preferably
φ1.1 mm or more, more preferably φ2.2 mm or more, and more preferably φ3.0 mm or more,
whereby clogging of the orifices can be suppressed and stable spraying can be maintained.
Since the fuel including combustible wastes sometimes includes waste textile, wastepaper,
waste rubber, mineral sludge, and the like, clogging of the orifices can be suppressed
by controlling the diameter of the orifices, as described above. No maximum limit
is set to the value of the diameter of the orifices; it may be any value as long as
the spray can maintain a spray state such that stable combustion is maintained.
[0033] The temperature in the furnace, when the fuel including combustible wastes is sprayed
into the furnace, is preferably set to 150°C or higher, and more preferably to 500°C
or higher. The moving hearth furnace is preferably operated such that a pilot burner
disposed in the vicinity of a position at which the fuel is sprayed ignites the fuel.
That is, when the fuel is sprayed into the furnace in which the temperature is set
to 150°C or higher, the moisture contained in the fuel vaporizes and only combustible
substances remain, whereby the fuel burns efficiently. The combustion starts smoothly
with the pilot burner igniting the fuel, thereby preventing the fuel including combustible
wastes from being sprayed into the furnace without being ignited. On the other hand,
when the temperature in the furnace is lower than 150°C, the fuel including combustible
wastes is not adequately ignited nor burned, and it is difficult to provide a stable
combustion state.
[0034] As a result of confirmation by the inventions, when the temperature in the furnace
is set to 600°C or higher, or preferably to 1000°C or higher, the fuel including combustible
wastes is self-ignited, and a stable combustion state is obtained.
[0035] Although the method of spraying the fuel including combustible wastes is not particularly
specified, a method which uses compressed air or vapor as a spraying medium may be
used. However, since the water content in the fuel must be kept as small as possible
in order to maintain a stable combustion in the furnace, it is preferable to use compressed
air.
<2> Case of pouring the fuel into the moving hearth furnace
[0036] According to the present invention, the fuel including combustible wastes may be
supplied by being poured onto the hearth of the moving hearth furnace, whereby the
fuel can be easily supplied. The position from which the fuel is poured is not particularly
specified. The fuel may be poured through an inlet for supplying a metal oxide into
the furnace, or a supply port for the fuel may be provided in the furnace wall or
ceiling.
[0037] It is recommended to control the flow of the fuel while measuring the amount of supply
of the fuel, which is sprayed (in the above method <1>) or is poured (in the above
method <2>) into the furnace, by using a flowmeter. In this case, there is a risk
in that the flowmeter is damaged or cannot maintain stable supply when it is a positive-displacement
meter because the fuel including combustible wastes generally includes sludge and
the like. Therefore, when a flowmeter is used in the line of supply of the fuel, it
is preferably an electromagnetic flowmeter or a Coriolis-type flowmeter which has
no moving parts in the line. However, when the electric conductivity of the fuel is
low and instable, measurement by using an electromagnetic flowmeter is difficult;
therefore, a Coriolis-type flowmeter is most preferable.
<3> Case of mixing the fuel including combustible wastes and a metal oxide (raw material)
and supplying the mixture into a moving hearth furnace
[0038] According to the present invention, a metal oxide as a raw material for manufacturing
a metal and the fuel including combustible wastes may be mixed with each other so
as to form agglomerate, and the agglomerated mixture may be supplied into the furnace
such that the fuel is burned in the furnace. When a method in which the fuel is mixed
in advance with a raw material to be reduced is used, the fuel can also serve as a
binder and the amount of binder for forming agglomerate of the raw material can be
thereby reduced. A carbonaceous reducing agent which is necessary for the reduction
of a metal oxide is preferably mixed with the agglomerated raw material.
[0039] Any type of carbonaceous reducing agent, such as pulverized coal processed simply
through crushing, screening, and the like after mining, crushed coke, for example,
processed by heating such as dry distillation, or petroleum coke, may be used. For
example, blast furnace dust collected as wastes including carbon may be also used.
However, since the carbonaceous reducing agent is used for efficiently advancing reduction
reaction by heating, the carbon content, which is not strictly specified though, is
preferably 70% or more by mass, and more preferably 80% or more by mass.
[0040] The above agglomerated mixture includes the mixture formed in an arbitrary shape
such as an lump shape, a granule shape, a briquette-shape, a pellet-shape, and a rod-shape.
The method of agglomeration is not particularly specified. For example, tumbling granulation
or pressing may be used.
[0041] According to the present invention, when the fuel is poured into a moving hearth
furnace (in the method <2>) or the fuel is mixed with a metal oxide and is supplied
into the moving hearth furnace (in the method <3>), the temperature in the furnace
is preferably set to 1100°C or higher, more preferably to 1200°C or higher, or more
preferably to 1250°C or higher, and the residence time of the fuel in the furnace
is preferably set to 3 minutes or longer, more preferably to 5 minutes or longer,
or more preferably to 7 minutes or longer. When the temperature in the furnace is
lower than 1100°C, the combustion of the fuel including combustible wastes is instable,
and a part of the fuel remains unburned, the part of the fuel being discharged to
the outside of the system without being burned, whereby there is a risk of reduction
of the utilization efficiency. When the residence time of the fuel in the furnace
is shorter than 3 minutes, a part of the fuel may remain unburned. The residence time
of 3 minutes or longer does not mean that the fuel remains in the same form as when
it was supplied into the furnace, but that it takes at least 3 minutes for the fuel
to completely burn out after the fuel is supplied into the furnace.
[0042] When the fuel including combustible wastes burns in the moving hearth furnace, a
sulfur oxide such as SO
x, or gaseous chlorine such as Cl
2 or HCl is generated from sulfur or chlorine included in the wastes and is discharged
as exhaust gas. The acid gas causes acid corrosion or corrosion by low melting temperature
compound and also air pollution.
[0043] Accordingly, the inventors studied means to avoid problems caused by the acid gas.
As a result, it was found that an alkali metal contained in the fuel serves to avoid
the problems. When an alkali metal is included in the fuel, the alkali metal is simultaneously
vaporized during combustion and is discharged as exhaust gas. In the high-temperature
exhaust gas, the alkali metal reacts with Cl in the exhaust gas and is solidified
as an alkali chloride such as NaCl or KCl. In the same manner, SO
x in the exhaust gas reacts with the alkali metal and is solidified as a sulfate such
as Na
2SO
4 or K
2SO
4. When the exhaust gas containing the alkali chloride and the sulfate is cooled in
exhaust-gas treatment facilities, the alkali chloride and the sulfate are separated
and the concentration of chlorine and sulfur in the exhaust gas can be thereby lowered.
Therefore, desulfurization and dechlorination facilities are not required and the
amount of use of slaked lime can be reduced.
[0044] When carrying out the present invention, the amount of the alkali metal to be blended
with the fuel is preferably controlled in accordance with the amount of S or Cl which
is generated in the furnace during reduction by heating. With this arrangement, chloric
gas such as Cl
2 or HCl and sulfur oxides such as SO
x are prevented from being discharged to the outside. The above-described chlorine
and sulfur can be captured in the same fashion by an alkali metal component which
may be contained in the agglomerate (for example, oxide-containing cores) to be used
for the manufacture of a reduced metal. However, since the alkali metal contained
in the fuel is released into exhaust gas more efficiently than the alkali metal contained
in the agglomerate, it is more effective to control the amount of the alkali metal
contained in the fuel.
[0045] In consideration of the above, according to the present invention, the amount of
the alkali metal to be blended and the amount of S and Cl generated in the furnace
are preferably controlled so as to satisfy the following expression.

[0046] In the expression (1), "other fuel" means additional fuel which does not include
a combustible waste. The examples of "other fuel" are heavy oil, pulverized coal and
so on.
[0047] Although the method of adding the alkali metal to the fuel is not particularly specified,
a method of adding a lubricant containing the alkali metal to the fuel may be used.
By controlling the amount of the lubricant to be blended, the amount of the alkali
metal can be easily controlled.
[0048] S and Cl captured by the alkali metal pass a bag filter mounted in exhaust-gas treating
facilities, in which there is a problem in that the alkali metal in collecting dust
increases, thereby increasing moisture absorption by and deliquescence of the dust
and clogging the bag filter. Therefore, a casing of the bag filter disposed in the
facilities for treating the exhaust gas of the moving hearth furnace is preferably
heat-insulated so that the surface temperature of the bag filter is higher than the
acid dew point by at least 10°C. With this arrangement, the moisture in the exhaust
gas is prevented from condensation in the bag filter, thereby suppressing clogging
of the bag filter.
[0049] According to the present invention, the above-described fuel may be used as a fuel
for the burner disposed in the furnace, or may be used as an auxiliary fuel by being
supplied through a supply port (for example, a spray) disposed in addition to the
burner. The present invention is also applicable to a case in which the above-described
fuel including combustible wastes is used as a mixture with a conventional fuel (for
example, heavy oil). The moving hearth furnace according to the present invention
is not particularly specified. The present invention is also applicable to a rotary-hearth
furnace or a straight hearth furnace .
[0050] The present invention is described below further in detail according to embodiments.
The invention is not limited to these embodiments, and the embodiments may be modified
in design within the technical scope of the present invention to the effect described
above and below.
[0051] Fig. 1 shows a rotary-hearth furnace used for reduction by heating of a metal oxide
and exhaust-gas treating facilities for exhaust gas discharged during the reduction
by heating. Numeral 5 in the drawing denotes a rotary-furnace (extension of a rotary-furnace
shown in Fig. 2). The exhaust gas from the rotary-hearth furnace produced during the
reduction by heating of the metal oxide flows via a path 11. Coarse powder dust and
the like are removed from the exhaust gas in a gas-cooling tower 21. The treated exhaust
gas flows via a path 12 into a heat exchanger 23, and is cooled by exchanging heat
with the air supplied by an air blower 22. The heated air as combustion air is supplied
via a path 14 to a burner which is mounted to the rotary-hearth furnace 5. The surplus
heated-air is discharged via a path 13 and is used as a heat source for related facilities
(boiler and the like).
[0052] The exhaust gas cooled by exchanging heat in the heat exchanger 23 is sent to an
off-gas bag filter 24 for cleaning via a path 15 and is released from a stack 26 via
a path 16 and an ID fan 25.
[0053] A fuel such as heavy oil or natural gas is supplied to the rotary-hearth furnace
5 via a line 17, and another fuel including combustible wastes is supplied thereto
via a line 10.
[0054] Figs. 2 to 4 are schematic illustrations for describing in detail the rotary-hearth
furnace 5 shown in Fig. 1, the rotary-hearth furnace 5 including a dome structure
having a donut-shaped rotary hearth. Fig. 2 is a schematic perspective view. Fig.
3 is a sectional view along line A-A of the rotary-hearth furnace 5 shown in Fig.
2. Fig. 4 is a schematic sectional view of the rotary-hearth furnace shown in Fig.
2 extended in the rotational direction thereof for facilitating description. Numeral
1 in the drawings denotes a rotary hearth and numeral 2 denotes a furnace body which
covers the rotary hearth. The rotary hearth 1 can be driven for rotation at a proper
speed by a driving mechanism not shown.
[0055] A plurality of burners 3 are provided at appropriate positions of walls of the furnace
body 2. Combustion heat of the burners 3 and radiation heat therefrom are transferred
to an agglomerate on the rotary hearth 1, thereby reducing by heating the formed body.
The inside of the furnace body 2 is divided into a first zone Z
1, a second zone Z
2, an exhaust zone, a third zone Z
3, and a fourth zone Z
4 by four baffle walls K
1, K
2, K
3, and K
4. Loading means 4 for raw materials and raw-material additives is disposed opposing
the rotary hearth 1 at the uppermost streamside in the rotational direction of the
furnace body 2. Discharging means 6 for a reduced metal produced by reduction by heating
is provided at the lowermost streamside in the rotational direction (and directly
upstream the loading means 4 in the rotational direction).
[0056] In the operation of the reduction furnace, an agglomerate including iron oxide waste
generated in a steel mill and a carbonaceous material is supplied by the loading means
4 so as to accumulate by an appropriate thickness on the rotary hearth 1 which rotates
at a given speed. The zones Z
1 to Z
4 are heated by the burners 3 so that the temperature therein becomes 1100°C to 1350°C.
The burners 3 are supplied with a fuel such as heavy oil or natural gas via the line
17 and with combustion air via the path 14.
[0057] Although according to the present embodiment, the burners 3 are disposed at the sidewalls,
the burners 3 may be disposed at the ceiling. The inside of the rotary furnace is
divided into each zone by the four baffle walls K
1 to K
4. However, the configuration of the furnace according to the present invention is
not limited to this embodiment, and it may be modified appropriately in accordance
with the size of the furnace, the targeted production capacity, the operation pattern,
and the like.
[Test 1]
[0058] The amount of supply of natural gas was compared between a case in which the burners
3 shown in Fig. 3 were supplied with natural gas as a fuel for manufacturing a reduced
metal and another case in which a fuel including combustible wastes was supplied to
sprays 7, which were provided in addition to the burners 3, and was burned in the
furnace as an auxiliary fuel. The burners 3 are supplied with the natural gas from
the line 17 and with heated air via the path 14. The sprays 7 are supplied with the
fuel including combustible wastes from the line 10 and with the heated air via the
path 14, and spray the fuel into the furnace with compressed air supplied via a path
18. Pilot burners 8 are provided in the vicinities of the sprays 7 for igniting the
fuel.
[0059] A material including iron-oxide-containing dust was used as a metal oxide, which
was formed as pellets having sizes of approximately 12 to 18 mm by using a disc pelletizer
having a diameter of 3000 mm. Regarding the content of carbon, the carbon concentration
is controlled in accordance with the requirement for the reduction of the metal oxide
and the downstream melting process.
[0060] A mixture of waste mineral oil, waste vegetable oil, waste animal oil, and the like
was used as the fuel including combustible wastes (hereinafter sometimes referred
to simply as "the fuel"), and was controlled so as to have a viscosity of 15 cP at
25°C and a higher calorific value of 18.0 to 21.3 MJ/kg. The composition of the fuel
is shown in table 1. The fuel contains moisture of 37 to 49% by mass.
Table 1
Composition (% by mass) |
C |
H |
N |
O |
S |
38 to 46 |
10 to 12 |
0.5 to 1.5 |
37 to 50 |
0.1 to 0.5 |
[0061] When only the burners 3 shown in Fig. 3 were used for reducing by heating a metal
oxide included in pellets weighing 2000 kg which were loaded by the loading means
4 for raw materials and raw-material additives for the rotary-hearth furnace shown
in Fig. 4, the calorific value required of the combustion heat from the supply gas
was 20.9 GJ. When the burners 3 and the sprays 7 were together used, the calorific
value of 6.3 GJ required of the combustion heat from the supply gas was sufficient.
That is, according to the present invention, the fuel cost can be significantly reduced.
[Test 2]
[0062] The relationship between the diameter of the orifices of the sprays 7 and clogging
of the orifices was studied, in which the fuel including combustible wastes was sprayed
into the furnace by using the sprays 7 while changing the diameter of the orifices
of the sprays 7. As a result, the orifices clogged in approximately 15 minutes after
the spray of the fuel started when the diameter of the orifices was 0.6 mm, and the
spray of the fuel could not continue. On the other hand, when the diameter of the
orifices was set to 1.1 mm, the spray of the fuel could continue for an hour without
cleaning of the orifices. When the diameter of the orifices was set to 2.2 mm, the
fuel could continue to be stably sprayed for 24 hours without cleaning of the orifices.
[Test 3]
[0063] A flowmeter to be appropriately used for measuring the flow rate (spray amount) of
the fuel was studied. As a result, measurement by using a positive displacement meter
was impossible because foreign substances included in the fuel were bitten. When an
electromagnetic flowmeter was used, the fuel could continue to be sprayed because
there were no moving parts in flow paths. However, electric conductivity varied according
to the variation in the composition of the fuel, whereby the flow amount could not
be correctly measured sometimes. A stable measurement was possible with a Coriolis-type
flowmeter.
[Test 4]
[0064] The relationship between the temperature in the furnace and the combustion of the
fuel was studied. As shown in Fig. 3, the sprays 7 were provided and the pilot burners
8 were disposed in the vicinities of the sprays 7. The fuel was sprayed by the sprays
7 and was burned. As a result, the pilot burners 8 did not ignite the fuel when the
temperature in the furnace was 100°C. When the temperature in the furnace was increased
to 200°C, the fuel was ignited and burned although slightly instable. When the temperature
in the furnace was increased to 560°C, the fuel was ignited immediately after it was
sprayed into the furnace and a stable combustion state could be maintained. Therefore,
the temperature in the furnace is preferably controlled so as to be not lower than
150°C in order to stably ignite and burn the fuel.
[Test 5]
[0065] The relationship between the temperature in the furnace and the combustion of the
fuel was studied, in which the fuel was supplied by being sprayed by the sprays 7
shown in Fig. 3 and the pilot burners 8 were not used. The temperature in the zone
Z1 of the furnace was controlled so as to be 500°C, 700°C, and 1000°C and the combustion
state of the fuel sprayed into the furnace at each temperature was monitored. As a
result, combustion was difficult and the fuel was not self-ignited at a temperature
of 500°C in the furnace. When the temperature in the furnace was 700°C, the fuel was
burned although slightly instable. When the temperature in the furnace was 1000°C,
the fuel was self-ignited. Since the calorific value of the fuel varies depending
on the composition thereof, the temperature in the furnace is preferably not lower
than 600°C so that the fuel including combustible wastes sprayed into the furnace
is burned (self-burned).
[Test 6]
[0066] The effect on reduction of the amount of gas was studied, in which a mixture of mixed
dust of the metal oxide, a carbonaceous reducing agent, and the fuel including combustible
wastes formed as pellets (briquettes) was loaded into the furnace. Five units of mass
of the fuel including combustible wastes and 100 units of mass of the dust of the
metal oxide mixed with each other were kneaded by a mixer, were compression-molded
to be formed as pellets, and were thrown into the furnace by the loading means 4 for
raw materials and raw-material additives. Only the burners 3 were used as a heat source
for the reduction by heating. As a result, the calorific value from the gas as a fuel
for the burners 3 required for reducing by heating the mixed dust of 1 ton could be
reduced by 0.4 GJ, in comparison with the case where the fuel does not include combustible
wastes.
[Test 7]
[0067] The fuel was poured, without using the sprays 7, into the zone Z
1 shown in Fig. 4 of the furnace. The fuel was poured into the furnace through a fuel-pouring
nozzle 9 shown in Fig. 3 (although the fuel was poured into the furnace from an upper
part thereof, it may be poured from a wall or the like). As a result, although the
fuel was accumulated on the pellets immediately after it was poured, it was found
to have been burned out from the hearth when viewed approximately 3 minutes after
the fuel was poured. No fuel content was detected in the mixed-dust agglomerates (reduced
agglomerates) which were discharged approximately 12 minutes after the fuel was poured
into the furnace. In this case, the calorific value from the supply gas for the burners
3 could be reduced by 2.1 GJ, in comparison with the case where the fuel does not
include combustible wastes.
[0068] When the viscosity of the fuel increases, the fuel becomes difficult to diffuse in
the furnace. Therefore, it is difficult to advance combustion of the fuel. However,
the inventors confirmed that the poured fuel having a viscosity of 50 cP at 20°C was
completely burned in approximately 5 minutes. In this case, the calorific value from
the burners 3 could be reduced also by 2.1 GJ.
[Test 8]
[0069] The effect of an alkali metal contained in the fuel including combustible wastes
was studied.
[0070] The amount of the alkali metal to be included in the fuel was controlled by adding
a lubricant which contains the alkali metal to the fuel including combustible wastes.
The compositions (only S, Cl, Na, and K) of the fuel which satisfies the above expression
(1) are shown in table 2, the fuel being referred to as "fuel containing alkali metal"
in the table. A fuel of which the content of alkali metal is less than 0.1% per chemical
element is referred to as "fuel not containing alkali metal". The result of computation
by using the above expression (1) is as follows.

<In the case of the fuel containing an alkali metal>
[0071] 
<In the case of the fuel not containing alkali metal>
[0072] 
[0073] The higher calorific value is 18.8 MJ/kg in both cases.
Table 2
|
Composition (% by mass) |
|
S |
Cl |
Na |
K |
Fuel containing alkali metal |
0.5 |
0.1 |
0.5 |
0.2 |
Fuel not containing alkali metal |
0.5 |
0.1 |
below
0.1 |
below
0.1 |
[0074] Agglomerate including a metal oxide having a weight of 2000 kg was reduced by heating
by using a "fuel containing an alkali metal" and another "fuel not containing alkali
metal", and the volumes of generated SO
x and HCl were measured at a section (A) shown in Fig. 1. The result is shown in table
3.
Table 3
|
SOx |
Cl-based gas |
Case of fuel containing alkali metal |
24 ppm |
40 ppm |
Case of fuel not containing alkali metal |
30 ppm |
60 ppm |
[0075] As shown in table 3, SO
x and a chloric gas such as HCl included in exhaust gas which is generated during reduction
by heating of a metal can be reduced when an alkali metal is contained in the fuel
including combustible wastes so that the above expression (1) is satisfied.
[Test 9]
[0076] The operational conditions of a bag filter provided in the exhaust-gas treating facilities
of the rotary-hearth furnace were studied. Clogging of the filter was monitored while
the casing of the bag filter was not heat insulated and while it was heat insulated.
As a result, the filter was clogged in approximately one month when it was not heat
insulated. When temperature at the surface of the filter fabric was kept higher than
the acid dew point by 10°C, the moisture contained in the exhaust gas was not condensed,
and clogging of the bag filter due to condensation of the alkali metal could be suppressed.