CA2534863A1 - Process and plant for reducing solids containing iron oxide - Google Patents
Process and plant for reducing solids containing iron oxide Download PDFInfo
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- CA2534863A1 CA2534863A1 CA002534863A CA2534863A CA2534863A1 CA 2534863 A1 CA2534863 A1 CA 2534863A1 CA 002534863 A CA002534863 A CA 002534863A CA 2534863 A CA2534863 A CA 2534863A CA 2534863 A1 CA2534863 A1 CA 2534863A1
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- iron oxide
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- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22B—PRODUCTION AND REFINING OF METALS; PRETREATMENT OF RAW MATERIALS
- C22B5/00—General methods of reducing to metals
- C22B5/02—Dry methods smelting of sulfides or formation of mattes
- C22B5/18—Reducing step-by-step
-
- C—CHEMISTRY; METALLURGY
- C21—METALLURGY OF IRON
- C21B—MANUFACTURE OF IRON OR STEEL
- C21B13/00—Making spongy iron or liquid steel, by direct processes
- C21B13/0033—In fluidised bed furnaces or apparatus containing a dispersion of the material
-
- C—CHEMISTRY; METALLURGY
- C21—METALLURGY OF IRON
- C21B—MANUFACTURE OF IRON OR STEEL
- C21B13/00—Making spongy iron or liquid steel, by direct processes
- C21B13/008—Use of special additives or fluxing agents
-
- C—CHEMISTRY; METALLURGY
- C21—METALLURGY OF IRON
- C21B—MANUFACTURE OF IRON OR STEEL
- C21B13/00—Making spongy iron or liquid steel, by direct processes
- C21B13/0086—Conditioning, transformation of reduced iron ores
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22B—PRODUCTION AND REFINING OF METALS; PRETREATMENT OF RAW MATERIALS
- C22B1/00—Preliminary treatment of ores or scrap
- C22B1/14—Agglomerating; Briquetting; Binding; Granulating
- C22B1/24—Binding; Briquetting ; Granulating
- C22B1/248—Binding; Briquetting ; Granulating of metal scrap or alloys
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22B—PRODUCTION AND REFINING OF METALS; PRETREATMENT OF RAW MATERIALS
- C22B5/00—General methods of reducing to metals
- C22B5/02—Dry methods smelting of sulfides or formation of mattes
- C22B5/12—Dry methods smelting of sulfides or formation of mattes by gases
- C22B5/14—Dry methods smelting of sulfides or formation of mattes by gases fluidised material
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P10/00—Technologies related to metal processing
- Y02P10/10—Reduction of greenhouse gas [GHG] emissions
- Y02P10/134—Reduction of greenhouse gas [GHG] emissions by avoiding CO2, e.g. using hydrogen
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- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Manufacturing & Machinery (AREA)
- Organic Chemistry (AREA)
- Metallurgy (AREA)
- Materials Engineering (AREA)
- Mechanical Engineering (AREA)
- Geology (AREA)
- Geochemistry & Mineralogy (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Life Sciences & Earth Sciences (AREA)
- Environmental & Geological Engineering (AREA)
- Dispersion Chemistry (AREA)
- Manufacture And Refinement Of Metals (AREA)
- Manufacture Of Iron (AREA)
Abstract
This invention relates to a process for reducing solids containing iron oxide, such as iron ore, in which fine-grained solids are heated and at least partly calcined in a pre heating stage (2, 9). In a first fluidized-bed reactor (14) downstream of the preheating stage (2, 9), the solids are prereduced and reduced further in a second fluidized-bed reactor (16). Downstream of the second reactor (16) a briquetting stage (20) is pro vided, in which the solids are briquetted at a temperature above 500~C To increase the energy efficiency of the process and improve the flowability of the solids in the briquetting stage (20), magnesite is added to the preheating stage (2, 9) together with the solids containing iron oxide, which magnesite is at least partly calcined in the preheating stage (2, 9) to obtain magnesium oxide. Furthermore, the invention relates to a corresponding plant.
Description
s ~ CA 02534863 2006-02-06 ~PCTIEP200 4 / 0 0 7 9 Q 4 '" _1_ PROCESS AND PLANT FOR REDUCING SOLIDS CONTAINING IRON OXIDE
The present invention relates to a process and a plant for reducing solids containing iron oxide, in particular iron ore, in which fine-grained solids are heated and at least partly calcined in a preheating and/or calcining stage, are prereduced in a first fluidized-bed reactor downstream of the preheating and/or calcining stage, and are reduced in a second fluidized-bed reactor and briquetted in a briquetting stage downstream of the second reactor at a temperature above 500°C.
From DE 44 10 093 C1 there is known such a process for the direct reduction of iron ores to obtain sponge iron (DRI), in which in a first reactor with circulating fluidized bed a prereduction is effected at temperatures between 550 and 650°C. In a downstream second reactor with classical fluidized bed, into which heated gas containing hydrogen is introduced as reducing agent for fluidizing purposes, the solids are further reduced, so that the product for instance has a degree of metallization of more than 90%.
During the transport of sponge iron (DRI), the iron is usually briquetted for safety rea-sons, for instance because of the risk of fire and because of the better handling (forma-tion of dust). Such briquetting is effected subsequent to the reduction of the iron, the still hot sponge iron mostly being cooled while being supplied to the briquetting plant.
For increasing the strength of the briquet it is, however, desirable that briquetting takes place at rather high temperatures of e.g. about 700°C. At this temperature, however, the fine-grained sponge iron has a very poor flow behavior, which makes briquetting more difficult. To improve the flow behavior of spong iron and ensure a good proc-essability, about 0.5 wt-% magnesium oxide (Mg0) is added to the sponge iron prior to briquetting through a pressure feeder upstream of the briquetting plant.
Magnesium oxide has no measurable negative influence on the strength or stability of the sponge iron briquet, but it is expensive due to costly processing steps, so that the manufactur-ing costs for sponge iron briquets are also rising. In addition, magnesium oxide is hygroscopic and very fine-grained, usually with a grain size below 100 Nm, so that it is difficult to store and to use.
13 July 2004 O 1 P 96 WO
The present invention relates to a process and a plant for reducing solids containing iron oxide, in particular iron ore, in which fine-grained solids are heated and at least partly calcined in a preheating and/or calcining stage, are prereduced in a first fluidized-bed reactor downstream of the preheating and/or calcining stage, and are reduced in a second fluidized-bed reactor and briquetted in a briquetting stage downstream of the second reactor at a temperature above 500°C.
From DE 44 10 093 C1 there is known such a process for the direct reduction of iron ores to obtain sponge iron (DRI), in which in a first reactor with circulating fluidized bed a prereduction is effected at temperatures between 550 and 650°C. In a downstream second reactor with classical fluidized bed, into which heated gas containing hydrogen is introduced as reducing agent for fluidizing purposes, the solids are further reduced, so that the product for instance has a degree of metallization of more than 90%.
During the transport of sponge iron (DRI), the iron is usually briquetted for safety rea-sons, for instance because of the risk of fire and because of the better handling (forma-tion of dust). Such briquetting is effected subsequent to the reduction of the iron, the still hot sponge iron mostly being cooled while being supplied to the briquetting plant.
For increasing the strength of the briquet it is, however, desirable that briquetting takes place at rather high temperatures of e.g. about 700°C. At this temperature, however, the fine-grained sponge iron has a very poor flow behavior, which makes briquetting more difficult. To improve the flow behavior of spong iron and ensure a good proc-essability, about 0.5 wt-% magnesium oxide (Mg0) is added to the sponge iron prior to briquetting through a pressure feeder upstream of the briquetting plant.
Magnesium oxide has no measurable negative influence on the strength or stability of the sponge iron briquet, but it is expensive due to costly processing steps, so that the manufactur-ing costs for sponge iron briquets are also rising. In addition, magnesium oxide is hygroscopic and very fine-grained, usually with a grain size below 100 Nm, so that it is difficult to store and to use.
13 July 2004 O 1 P 96 WO
A process of producing sponge iron from oxidic iron ores is also known from DE-458 756, in which the reduction should be effected at rather high temperatures. To avoid an effect known as bogging or fouling, which occurs during the reduction at such high temperatures and in which the solids stick or weld together to form agglomerates, so that the fluidized bed sinks down in the reduction reactor, the addition of about 0.05 wt-% of very finely ground oxides or carbonates of magnesium is proposed.
These additives should be rather fine-grained and preferably have a grain size of distinctly less than 297 pm, in particular less than 44 pm. However, this also leads to the above-described problems during the storage or use of the additives. In addition, in this proc-ess the additives must be added to the iron ore e.g. via a pressure feeder before the reduction stage. This leads to a rise in the investment costs for a plant for performing the process. Due to the lower temperatures in the reduction stage, a comparatively poor calcination is achieved in this known process, when carbonates of magnesium are added to the reduction stage. This can only be compensated by longer retention times, which are, however, likewise undesirable. On the other hand, these problems do not occur when magnesium oxide is added to the reduction stage instead of carbonates of magnesium. However, this involves the above-mentioned disadvantages of the high costs and the poor handling properties of magnesium oxide.
Therefore, it is the object of the present invention to provide a process and a plant for reducing solids containing iron oxide, which is characterized by an improved flow be-havior of the product and a lower consumption of energy.
In accordance with the invention, this object is solved by a process as mentioned above, in which magnesite (MgC03) together with the solids containing iron oxide is added to the preheating andlor calcining stage, which magnesite is at least partly calcined in the preheating and/or calcining stage to obtain magnesium oxide.
As com-pared to magnesium oxide, magnesite is available at a distinctly lower price, so that the costs for producing briquets from sponge iron can be decreased. Since the magnesite is at least partly calcined to obtain magnesium oxide, the flowability of the sponge iron prior to briquetting is improved. Briquetting therefore can also take place at high tem-peratures, at which the flow behavior of the sponge iron usually is deteriorated. By means of this hot briquetting, the strength of the briquet is increased as compared to cold briquetting at lower temperatures.
These additives should be rather fine-grained and preferably have a grain size of distinctly less than 297 pm, in particular less than 44 pm. However, this also leads to the above-described problems during the storage or use of the additives. In addition, in this proc-ess the additives must be added to the iron ore e.g. via a pressure feeder before the reduction stage. This leads to a rise in the investment costs for a plant for performing the process. Due to the lower temperatures in the reduction stage, a comparatively poor calcination is achieved in this known process, when carbonates of magnesium are added to the reduction stage. This can only be compensated by longer retention times, which are, however, likewise undesirable. On the other hand, these problems do not occur when magnesium oxide is added to the reduction stage instead of carbonates of magnesium. However, this involves the above-mentioned disadvantages of the high costs and the poor handling properties of magnesium oxide.
Therefore, it is the object of the present invention to provide a process and a plant for reducing solids containing iron oxide, which is characterized by an improved flow be-havior of the product and a lower consumption of energy.
In accordance with the invention, this object is solved by a process as mentioned above, in which magnesite (MgC03) together with the solids containing iron oxide is added to the preheating andlor calcining stage, which magnesite is at least partly calcined in the preheating and/or calcining stage to obtain magnesium oxide.
As com-pared to magnesium oxide, magnesite is available at a distinctly lower price, so that the costs for producing briquets from sponge iron can be decreased. Since the magnesite is at least partly calcined to obtain magnesium oxide, the flowability of the sponge iron prior to briquetting is improved. Briquetting therefore can also take place at high tem-peratures, at which the flow behavior of the sponge iron usually is deteriorated. By means of this hot briquetting, the strength of the briquet is increased as compared to cold briquetting at lower temperatures.
Since the magnesite is heated in the preheating and/or calcining stage together with the solids containing iron oxide, the supply of heat to the two reactors for reducing the solids containing iron oxide need not be ensured by a strong heating of the reducing agent, e.g. hydrogen. The energy efficiency of the endothermal reduction process hence can be increased in that the solids containing iron oxide and the magnesite are heated already in the preheating andlor calcining stage to the temperature required for reduction.
Due to the common supply of the solids containing iron oxide and the magnesite into the preheating and/or calcining stage it is not necessary to add additional magnesium oxide to the solids before a pressure feeder upstream of the reactors. In this way, the investment costs for the commonly used separate supply of magnesium oxide are also eliminated. The magnesite frequently contains impurities such as iron oxide andlor limestone, which do not disturb the further processing steps, but are in part even de-sired for the further processing of the iron.
The energy efficiency of the process of the invention can further be increased in that the magnesite together with the solids containing iron oxide is calcined in the preheat-ing and/or calcining stage at temperatures of 400 to 1250°C, in particular at 540 to 1000°C. In accordance with the invention, the temperature range for calcining can also lie between 1000 and about 1250°C. Due to the particularly high temperatures in the preheating and/or calcining stage, as compared to the known processes, the supply of heat for the endothermal reduction of iron oxide by means of hydrogen need not be effected by a strong heating of the hydrogen commonly used as reducing agent.
In accordance with a preferred embodiment of the invention, more than 50 %, prefera-bly about 90 %, of the magnesite added to the preheating and/or calcining stage to-gether with the solids containing iron oxide have a grain size between 300 pm and 3 mm, in particular between 400 pm and 1 mm. For the process in accordance with the invention there can also be used magnesite with a grain size between 1.25 and 3 mm.
The storage and the handling properties of the magnesite are improved thereby without deteriorating the flowability of the sponge iron. In the course of the process, the rela-tively coarse-grained magnesite or the magnesium oxide is ground in the preheating and/or calcining stage or in the reactors provided downstream of the same. The appli-cability of the magnesium oxide in briquetting thereby is increased without deteriorating the handling properties of the additives.
An improved flow behavior and a good processability of sponge iron, in particular in the briquetting stage, is achieved in accordance with the invention when between 0.1 and 5 wt-%, in particular about 0.5 wt-% magnesite is added to the solids containing iron oxide before and/or during the supply into the preheating and/or calcining stage. The solids supplied to the briquetting stage from the second reactor contain for instance between 0.1 and 5 wt-°I°, in particular about 0.5 wt-°lo magnesium oxide, which was obtained by calcining the magnesite in the preheating and/or calcining stage.
To further improve the processability of the solids reduced in the second reactor in the briquetting stage, the same can be heated together with the magnesium oxide in a heating stage upstream of the briquetting stage to a temperature above 600°C, in particular about 700°C, and can be introduced into the briquetting stage in the hot condition. This pro-vides for a further reduction of the energy required for forming in the briquetting stage.
To largely avoid the formation of agglomerates in the reactors during the reduction, the solids containing iron oxide are reduced in the first and second reactors, preferably at temperatures below 700°C, in particular at about 630°C. At these temperatures, the bogging effect known from the prior art does not occur. As a result, the magnesite supplied to the preheating and/or calcining stage is not required already in the reduc-tion stage for forming magnesium oxide, but ensures the flowability of the sponge iron during the supply to a briquetting plant. The degree of fluidization of the solids contain-ing iron oxide in the first and second reactors hence is particularly high during the reduction, so that there can occur a good transfer of heat and a good reaction with the reducing agent. The solids containing iron oxide are reduced in the first and second reactors to obtain metallic iron with a degree of metallization of more than 75 %, in particular more than 90 %.
The object underlying the invention is further solved with a plant for reducing solids containing iron oxide, comprising a preheating and/or calcining stage, a first and a second reactor each constituting a fluidized-bed reactor, and a briquetting stage, in that the preheating stage includes means for the simultaneous continuous or discontinuous introduction of iron-oxide-containing solids and magnesite, and that upstream of the briquetting stage a heating stage is provided. Since iron-oxide-containing solids and magnesite are introduced together, the same are heated in the preheating and/or calcining stage, so that the heat required for the subsequent endothermal reduction of 5 the iron oxide need not be ensured by a strong heating of the reducing agent. The heating stage upstream of the briquetting stage also makes it possible that the sponge iron withdrawn from the reduction reactors together with magnesium oxide obtained from the magnesite can be heated to a temperature of for instance about 700°C, which is optimal for briquetting. The reduction can be effected at comparatively low tempera-tares, so that the inclination of the iron oxide to form agglomerates is largely sup-pressed.
The two series-connected reactors, in which the reduction takes place, can for instance be fluidized-bed reactors with a stationary fluidized bed. To provide for improved mass 15' and heat transfer conditions during the reduction, at least one of the two reactors should, however, preferably be a fluidized-bed reactor with a circulating fluidized bed or an annular fluidized bed.
In accordance with a preferred embodiment of the invention, the first and/or the second reactor has a plurality of nozzles or inlet openings for supplying a heated, gaseous reducing agent, such as hydrogen. The reducing agent can also be used for fluidizing the solids reduced in the reactors.
The energy efficiency of the plant in accordance with the invention can be improved in that the preheating and/or calcining stage includes a first preheater, for instance a Venturi preheater, with a downstream first cyclone and a second preheater (calcining stage) with a downstream second cyclone, the first and/or the second cyclone being connected with the first Venturi preheater via a conduit for recirculating dust separated from waste gas. The dust heated in the preheating and/or calcining stage thus is util-ized for preheating the solids containing iron oxide and the magnesite.
Further developments, advantages and possible applications of the invention can also be taken from the subsequent description of an embodiment and the drawing. All fea-tures described and/or illustrated in the drawing form the subject-matter of the invention per se or in any combination, independent of their inclusion in the claims or their back-reference.
The only Figure shows a process diagram of a process and a plant in accordance with an embodiment of the present invention. In the process for reducing solids containing iron oxide as shown in the Figure, for instance moist iron ore together with magnesite (MgC03) is introduced via a supply conduit 1 into a Venturi preheater 2, in which the solids containing iron oxide and the magnesite are dried and heated. Via conduit 3, the solids containing iron oxide together with the magnesite are introduced into a cyclone 4, in which the dust-laden waste gases are separated from solids.
Via conduit 5, the dust-laden waste gases are supplied to a filter 6, for instance an electrostatic precipitator or a scrubber, from which the dust is recirculated to the pre-heating stage via conduit 7.
The solids separated from the waste gas in the cyclone 4 are supplied via conduit 8 to a calcining stage 9 or a second preheater to which a burner 9a is associated, by means of which a major part of the energy is supplied to the process. In the calcining stage 9, the solids and the magnesite are preheated to a temperature of for instance about 850°C. Due to this high temperature in the calcining stage 9, the magnesite is calcined to obtain magnesium oxide, which together with the solids containing icon oxide is supplied via conduit 10 to a second cyclone 11. Therein, the solids are separated from .
dust-laden waste gas, which is supplied to the first Venturi preheater 2 via conduit 12.
As a result, the solids containing iron oxide and the magnesite are heated and dried in the Venturi preheater 2 by the waste gases of the second cyclone 11.
The solids separated in the second cyclone 11 are supplied via a conduit 13 with pres-sure feeder to a first reactor 14, which for instance includes a circulating fluidized bed.
By supplying hydrogen, the heated ore containing iron oxide is prereduced in the first reactor 14 and via conduit 15 introduced into a second reactor 16, which can be a stationary fluidized-bed reactor. Heated hydrogen as reducing agent is also introduced into the second reactor 16, so that the iron oxide is reduced in the second reactor 16.
Due to the common supply of the solids containing iron oxide and the magnesite into the preheating and/or calcining stage it is not necessary to add additional magnesium oxide to the solids before a pressure feeder upstream of the reactors. In this way, the investment costs for the commonly used separate supply of magnesium oxide are also eliminated. The magnesite frequently contains impurities such as iron oxide andlor limestone, which do not disturb the further processing steps, but are in part even de-sired for the further processing of the iron.
The energy efficiency of the process of the invention can further be increased in that the magnesite together with the solids containing iron oxide is calcined in the preheat-ing and/or calcining stage at temperatures of 400 to 1250°C, in particular at 540 to 1000°C. In accordance with the invention, the temperature range for calcining can also lie between 1000 and about 1250°C. Due to the particularly high temperatures in the preheating and/or calcining stage, as compared to the known processes, the supply of heat for the endothermal reduction of iron oxide by means of hydrogen need not be effected by a strong heating of the hydrogen commonly used as reducing agent.
In accordance with a preferred embodiment of the invention, more than 50 %, prefera-bly about 90 %, of the magnesite added to the preheating and/or calcining stage to-gether with the solids containing iron oxide have a grain size between 300 pm and 3 mm, in particular between 400 pm and 1 mm. For the process in accordance with the invention there can also be used magnesite with a grain size between 1.25 and 3 mm.
The storage and the handling properties of the magnesite are improved thereby without deteriorating the flowability of the sponge iron. In the course of the process, the rela-tively coarse-grained magnesite or the magnesium oxide is ground in the preheating and/or calcining stage or in the reactors provided downstream of the same. The appli-cability of the magnesium oxide in briquetting thereby is increased without deteriorating the handling properties of the additives.
An improved flow behavior and a good processability of sponge iron, in particular in the briquetting stage, is achieved in accordance with the invention when between 0.1 and 5 wt-%, in particular about 0.5 wt-% magnesite is added to the solids containing iron oxide before and/or during the supply into the preheating and/or calcining stage. The solids supplied to the briquetting stage from the second reactor contain for instance between 0.1 and 5 wt-°I°, in particular about 0.5 wt-°lo magnesium oxide, which was obtained by calcining the magnesite in the preheating and/or calcining stage.
To further improve the processability of the solids reduced in the second reactor in the briquetting stage, the same can be heated together with the magnesium oxide in a heating stage upstream of the briquetting stage to a temperature above 600°C, in particular about 700°C, and can be introduced into the briquetting stage in the hot condition. This pro-vides for a further reduction of the energy required for forming in the briquetting stage.
To largely avoid the formation of agglomerates in the reactors during the reduction, the solids containing iron oxide are reduced in the first and second reactors, preferably at temperatures below 700°C, in particular at about 630°C. At these temperatures, the bogging effect known from the prior art does not occur. As a result, the magnesite supplied to the preheating and/or calcining stage is not required already in the reduc-tion stage for forming magnesium oxide, but ensures the flowability of the sponge iron during the supply to a briquetting plant. The degree of fluidization of the solids contain-ing iron oxide in the first and second reactors hence is particularly high during the reduction, so that there can occur a good transfer of heat and a good reaction with the reducing agent. The solids containing iron oxide are reduced in the first and second reactors to obtain metallic iron with a degree of metallization of more than 75 %, in particular more than 90 %.
The object underlying the invention is further solved with a plant for reducing solids containing iron oxide, comprising a preheating and/or calcining stage, a first and a second reactor each constituting a fluidized-bed reactor, and a briquetting stage, in that the preheating stage includes means for the simultaneous continuous or discontinuous introduction of iron-oxide-containing solids and magnesite, and that upstream of the briquetting stage a heating stage is provided. Since iron-oxide-containing solids and magnesite are introduced together, the same are heated in the preheating and/or calcining stage, so that the heat required for the subsequent endothermal reduction of 5 the iron oxide need not be ensured by a strong heating of the reducing agent. The heating stage upstream of the briquetting stage also makes it possible that the sponge iron withdrawn from the reduction reactors together with magnesium oxide obtained from the magnesite can be heated to a temperature of for instance about 700°C, which is optimal for briquetting. The reduction can be effected at comparatively low tempera-tares, so that the inclination of the iron oxide to form agglomerates is largely sup-pressed.
The two series-connected reactors, in which the reduction takes place, can for instance be fluidized-bed reactors with a stationary fluidized bed. To provide for improved mass 15' and heat transfer conditions during the reduction, at least one of the two reactors should, however, preferably be a fluidized-bed reactor with a circulating fluidized bed or an annular fluidized bed.
In accordance with a preferred embodiment of the invention, the first and/or the second reactor has a plurality of nozzles or inlet openings for supplying a heated, gaseous reducing agent, such as hydrogen. The reducing agent can also be used for fluidizing the solids reduced in the reactors.
The energy efficiency of the plant in accordance with the invention can be improved in that the preheating and/or calcining stage includes a first preheater, for instance a Venturi preheater, with a downstream first cyclone and a second preheater (calcining stage) with a downstream second cyclone, the first and/or the second cyclone being connected with the first Venturi preheater via a conduit for recirculating dust separated from waste gas. The dust heated in the preheating and/or calcining stage thus is util-ized for preheating the solids containing iron oxide and the magnesite.
Further developments, advantages and possible applications of the invention can also be taken from the subsequent description of an embodiment and the drawing. All fea-tures described and/or illustrated in the drawing form the subject-matter of the invention per se or in any combination, independent of their inclusion in the claims or their back-reference.
The only Figure shows a process diagram of a process and a plant in accordance with an embodiment of the present invention. In the process for reducing solids containing iron oxide as shown in the Figure, for instance moist iron ore together with magnesite (MgC03) is introduced via a supply conduit 1 into a Venturi preheater 2, in which the solids containing iron oxide and the magnesite are dried and heated. Via conduit 3, the solids containing iron oxide together with the magnesite are introduced into a cyclone 4, in which the dust-laden waste gases are separated from solids.
Via conduit 5, the dust-laden waste gases are supplied to a filter 6, for instance an electrostatic precipitator or a scrubber, from which the dust is recirculated to the pre-heating stage via conduit 7.
The solids separated from the waste gas in the cyclone 4 are supplied via conduit 8 to a calcining stage 9 or a second preheater to which a burner 9a is associated, by means of which a major part of the energy is supplied to the process. In the calcining stage 9, the solids and the magnesite are preheated to a temperature of for instance about 850°C. Due to this high temperature in the calcining stage 9, the magnesite is calcined to obtain magnesium oxide, which together with the solids containing icon oxide is supplied via conduit 10 to a second cyclone 11. Therein, the solids are separated from .
dust-laden waste gas, which is supplied to the first Venturi preheater 2 via conduit 12.
As a result, the solids containing iron oxide and the magnesite are heated and dried in the Venturi preheater 2 by the waste gases of the second cyclone 11.
The solids separated in the second cyclone 11 are supplied via a conduit 13 with pres-sure feeder to a first reactor 14, which for instance includes a circulating fluidized bed.
By supplying hydrogen, the heated ore containing iron oxide is prereduced in the first reactor 14 and via conduit 15 introduced into a second reactor 16, which can be a stationary fluidized-bed reactor. Heated hydrogen as reducing agent is also introduced into the second reactor 16, so that the iron oxide is reduced in the second reactor 16.
From the second reactor 16, sponge iron with a high degree of metallization is with-drawn together with magnesium oxide and via conduit 17 introduced into a heating stage 18, in which the solids are heated to a temperature of about 700°C and via con-duit 19 are introduced into a briquetting stage 20 in the hot condition.
Downstream of the reactors 14 and 16 recirculating cyclones can be provided, in which dust-like solids are separated from the gases leaving the reactors. In a waste gas treatment stage 21, these waste gases can be cleaned and be heated in a heater 22, before they are recirculated to the reactors 14, 16.
Example (Reduction of Iron Ore) In a plant corresponding to the Figure, 61.2 t/h of moist iron ore with 7.8 %
moisture and 300 kg/h of magnesite with a grain size of less than 1 mm were supplied to the Venturi preheater 2 via conduit 1. Together with the magnesite, the iron ore was dried and heated in the Venturi preheater 2 and introduced via the cyclone 4 into the calcin-ing stage 9, in which the iron ore and the magnesite were heated to a temperature of 850°C.
From the dust-laden waste gases separated in the cyclone 4, 2.6 t/h of dust were separated in the filter 6, which dust contained 25 kg/h of magnesium oxide.
This dust was recirculated to the preheating stage via conduit 7.
54.2 t/h of the iron ore heated to 850°C in the preheater 9 together with 150 kg/h of magnesite calcined to magnesium oxide were introduced via conduit 13 with pressure feeder into the reactor 14 and the reactor 16 provided downstream of the same.
The reduction in the reactors 14 and 16 at a temperature of about 630°C
provided 37 t/h of a product with a degree of metallization of 91 %. The product which contained about 34 t/h of metallic iron and 150 kg/h of magnesium oxide was introduced via conduit 17 into the further heating stage 18. In the same, the metallic iron and the magnesium oxide were heated to 700°C and via conduit 19 were introduced into the briquetting stage 20 in the hot condition.
Downstream of the reactors 14 and 16 recirculating cyclones can be provided, in which dust-like solids are separated from the gases leaving the reactors. In a waste gas treatment stage 21, these waste gases can be cleaned and be heated in a heater 22, before they are recirculated to the reactors 14, 16.
Example (Reduction of Iron Ore) In a plant corresponding to the Figure, 61.2 t/h of moist iron ore with 7.8 %
moisture and 300 kg/h of magnesite with a grain size of less than 1 mm were supplied to the Venturi preheater 2 via conduit 1. Together with the magnesite, the iron ore was dried and heated in the Venturi preheater 2 and introduced via the cyclone 4 into the calcin-ing stage 9, in which the iron ore and the magnesite were heated to a temperature of 850°C.
From the dust-laden waste gases separated in the cyclone 4, 2.6 t/h of dust were separated in the filter 6, which dust contained 25 kg/h of magnesium oxide.
This dust was recirculated to the preheating stage via conduit 7.
54.2 t/h of the iron ore heated to 850°C in the preheater 9 together with 150 kg/h of magnesite calcined to magnesium oxide were introduced via conduit 13 with pressure feeder into the reactor 14 and the reactor 16 provided downstream of the same.
The reduction in the reactors 14 and 16 at a temperature of about 630°C
provided 37 t/h of a product with a degree of metallization of 91 %. The product which contained about 34 t/h of metallic iron and 150 kg/h of magnesium oxide was introduced via conduit 17 into the further heating stage 18. In the same, the metallic iron and the magnesium oxide were heated to 700°C and via conduit 19 were introduced into the briquetting stage 20 in the hot condition.
List of reference numerals:
1 conduit 2 (first) Venturi preheater 3 conduit 4 (first) cyclone 5 conduit 6 filter 7 conduit 8 conduit 9 calcining stage (second preheater) 9a burner 10 conduit 11 (second) cyclone 12 conduit 13 conduit with pressure feeder 14 (first) reactor 15 conduit 16 (second) reactor 17 conduit 18 heating stage 19 conduit 20 briquetting stage 21 waste gas treatment stage 22 heater
1 conduit 2 (first) Venturi preheater 3 conduit 4 (first) cyclone 5 conduit 6 filter 7 conduit 8 conduit 9 calcining stage (second preheater) 9a burner 10 conduit 11 (second) cyclone 12 conduit 13 conduit with pressure feeder 14 (first) reactor 15 conduit 16 (second) reactor 17 conduit 18 heating stage 19 conduit 20 briquetting stage 21 waste gas treatment stage 22 heater
Claims (12)
1. A process for reducing solids containing iron oxide, in particular iron ore, in which fine-grained solids are heated and at least partly calcined in a preheating and/or calcining stage (2, 9), are prereduced in a first fluidized-bed reactor (14) downstream of the preheating and/or calcining stage (2, 9), and are reduced in a second fluidized-bed reactor (16) and briquetted in a briquetting stage (20) downstream of the second reac-tor (16) at a temperature above 50°C, characterized in that magnesite together with the solids containing iron oxide is added to the preheating and/or calcining stage (2, 9), which magnesite is at least partly calcined in the preheating and/or calcining stage (2, 9) to obtain magnesium oxide.
2. The process as claimed in claim 1, characterized in that the magnesite to-gether with the solids containing iron oxide is calcined in the preheating and/or calcin-ing stage (2, 9) at temperatures of 400 to 1250°C, in particular at 540 to 1000°C.
3. The process as claimed in claim 1 or 2, characterized in that more than 50 %, in particular about 90 %, of the magnesite added to the preheating and/or calcining stage (2, 9) together with the solids containing iron oxide has a grain size between 300 pm and 3 mm, in particular between 400 pm and 1 mm.
4. The process as claimed in any of the preceding claims, characterized in that between 0.1 and 5 wt-%, in particular about 0.5 wt-% of magnesite are added to the solids containing iron oxide before and/or during the supply into the preheating and/or calcining stage (2, 9).
5. The process as claimed in any of the preceding claims, characterized in that the solids supplied to the briquetting stage (20) from the second reactor (16) contain between 0.1 and 5 wt-%, in particular about 0.5 wt-%, of magnesium oxide.
6. The process as claimed in any of the preceding claims, characterized in that in a heating stage (18) upstream of the briquetting stage (20) the solids reduced in the second reactor (16) together with the magnesium oxide are heated to a temperature above 600°C, in particular about 700°C, and are introduced into the briquetting stage (20) in the hot condition.
7. The process as claimed in any of the preceding claims, characterized in that the solids containing iron oxide are reduced in the first and second reactors (14, 16) at temperatures below 700°C, in particular at about 630°C, to obtain metallic iron with a degree of metallization of more than 75 %, in particular more than 90 %.
8. Use of magnesite as flux material which in a process for producing sponge iron briquets, in particular as claimed in any of the preceding claims, is charged together with solids containing iron oxide, in order to increase the flowability of hot sponge iron during the supply from a reduction stage into a briquetting stage.
9. A plant for reducing solids containing iron oxide, in particular for performing a process as claimed in any of claims 1 to 7, comprising a preheating and/or calcining stage (2, 9), a first and a second reactor (14, 16) each constituting a fluidized-bed reactor, and a briquetting stage (20), characterized in that the preheating and/or calcining stage (2, 9) includes means (1 ) for the simultaneous continuous or discon-tinuous introduction of iron-oxide-containing solids and magnesite, and that upstream of the briquetting stage (20) a heating stage (18) is provided.
10. The plant as claimed in claim 9, characterized in that at least one of the two reactors (14, 16) is a fluidized-bed reactor with a circulating fluidized bed and/or an annular fluidized bed.
11. The plant as claimed in claim 10, characterized in that the first and second reactors (14, 16) have a plurality of nozzles or inlet openings for supplying a heated gaseous reducing agent such as hydrogen.
12. The plant as claimed in any of claims 9 to 11, characterized in that the preheating and/or calcining stage (2, 9) includes a first Venturi preheater (2) with a downstream first cyclone (4) and a second preheater (9) with a downstream second cyclone (11), the first and/or the second cyclone (4, 11) being connected with the first Venturi preheater (2) via conduit (5, 7) for recirculating dust separated from waste gas.
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE10336676A DE10336676C5 (en) | 2003-08-09 | 2003-08-09 | Process and plant for the reduction of iron oxide-containing solids |
| DE10336676.8 | 2003-08-09 | ||
| PCT/EP2004/007904 WO2005014866A2 (en) | 2003-08-09 | 2004-07-16 | Process and plant for reducing solids containing iron oxide |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CA2534863A1 true CA2534863A1 (en) | 2005-02-17 |
Family
ID=34129525
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CA002534863A Abandoned CA2534863A1 (en) | 2003-08-09 | 2004-07-16 | Process and plant for reducing solids containing iron oxide |
Country Status (9)
| Country | Link |
|---|---|
| US (1) | US20070079666A1 (en) |
| CN (1) | CN100366757C (en) |
| AU (1) | AU2004262646A1 (en) |
| BR (1) | BRPI0413371A (en) |
| CA (1) | CA2534863A1 (en) |
| DE (1) | DE10336676C5 (en) |
| EA (1) | EA011430B1 (en) |
| WO (1) | WO2005014866A2 (en) |
| ZA (1) | ZA200600898B (en) |
Families Citing this family (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE102009038052B4 (en) | 2009-08-19 | 2012-09-27 | Wolfgang Krumm | Smelting process by using a pre-reduced Ilmeniterzstromes and / or Hematitezstromes |
| DE102015107433A1 (en) * | 2015-05-12 | 2016-11-17 | Outotec (Finland) Oy | Process and plant for the production of calcined petroleum coke |
| DE102016103349A1 (en) * | 2016-02-25 | 2017-08-31 | Outotec (Finland) Oy | Method and device for thermal treatment of a contaminated solid |
| CN109136539B (en) * | 2018-07-05 | 2020-06-23 | 沈阳化工大学 | Integrated process of fluidized bed two-stage gasification and flash light burning magnesite |
| CN115341061B (en) * | 2021-05-13 | 2024-01-02 | 中国科学院过程工程研究所 | Method for efficiently fluidizing and reducing vanadium titano-magnetite fine powder |
| DE102021205828A1 (en) * | 2021-06-09 | 2022-12-15 | Refratechnik Holding Gmbh | Process and apparatus for producing a calcined material |
Family Cites Families (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2792298A (en) * | 1954-04-09 | 1957-05-14 | Freeman Horace | Iron oxide reduction |
| DE1458756A1 (en) * | 1964-09-21 | 1969-02-06 | Esso Res & Engineering Company | Process for the production of sponge iron from oxidic iron ores |
| US3393066A (en) * | 1964-09-21 | 1968-07-16 | Exxon Research Engineering Co | Process for reduction of iron ore in staged fluid beds without bogging |
| AT404735B (en) * | 1992-10-22 | 1999-02-25 | Voest Alpine Ind Anlagen | METHOD AND INSTALLATION FOR THE PRODUCTION OF LIQUID PIPE IRON OR LIQUID STEEL PRE-PRODUCTS |
| DE4410093C1 (en) * | 1994-03-24 | 1995-03-09 | Metallgesellschaft Ag | Process for the direct reduction of materials containing iron oxides |
| DK0630975T3 (en) * | 1993-06-19 | 1997-09-01 | Metallgesellschaft Ag | Method for direct reduction of iron oxide-containing substances. |
| CN1070926C (en) * | 1997-12-20 | 2001-09-12 | 浦项综合制铁株式会社 | Apparatus for manufacturing molten pig iron and reduced iron by utilizing fluidized bed, and method therefor |
-
2003
- 2003-08-09 DE DE10336676A patent/DE10336676C5/en not_active Expired - Lifetime
-
2004
- 2004-07-08 ZA ZA200600898A patent/ZA200600898B/en unknown
- 2004-07-16 US US10/567,821 patent/US20070079666A1/en not_active Abandoned
- 2004-07-16 EA EA200600389A patent/EA011430B1/en not_active IP Right Cessation
- 2004-07-16 AU AU2004262646A patent/AU2004262646A1/en not_active Abandoned
- 2004-07-16 CN CNB2004800208324A patent/CN100366757C/en active Active
- 2004-07-16 CA CA002534863A patent/CA2534863A1/en not_active Abandoned
- 2004-07-16 BR BRPI0413371-4A patent/BRPI0413371A/en not_active IP Right Cessation
- 2004-07-16 WO PCT/EP2004/007904 patent/WO2005014866A2/en active Application Filing
Also Published As
| Publication number | Publication date |
|---|---|
| WO2005014866A3 (en) | 2005-03-31 |
| US20070079666A1 (en) | 2007-04-12 |
| AU2004262646A1 (en) | 2005-02-17 |
| BRPI0413371A (en) | 2006-10-17 |
| WO2005014866A2 (en) | 2005-02-17 |
| CN1826416A (en) | 2006-08-30 |
| CN100366757C (en) | 2008-02-06 |
| DE10336676C5 (en) | 2011-03-31 |
| ZA200600898B (en) | 2007-05-30 |
| EA011430B1 (en) | 2009-02-27 |
| EA200600389A1 (en) | 2006-08-25 |
| DE10336676A1 (en) | 2005-03-17 |
| DE10336676B4 (en) | 2005-09-29 |
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