SE545831C2 - Method for Producing Steel - Google Patents

Method for Producing Steel

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Publication number
SE545831C2
SE545831C2 SE2151144A SE2151144A SE545831C2 SE 545831 C2 SE545831 C2 SE 545831C2 SE 2151144 A SE2151144 A SE 2151144A SE 2151144 A SE2151144 A SE 2151144A SE 545831 C2 SE545831 C2 SE 545831C2
Authority
SE
Sweden
Prior art keywords
stream
predetermined amount
steel
iron ore
vessel
Prior art date
Application number
SE2151144A
Other languages
Swedish (sv)
Other versions
SE2151144A1 (en
Inventor
Stefan Källander
Torsten Granberg
Original Assignee
Plagazi Ab
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Plagazi Ab filed Critical Plagazi Ab
Priority to SE2151144A priority Critical patent/SE545831C2/en
Priority to PCT/SE2022/050806 priority patent/WO2023043358A1/en
Publication of SE2151144A1 publication Critical patent/SE2151144A1/en
Publication of SE545831C2 publication Critical patent/SE545831C2/en

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22BPRODUCTION AND REFINING OF METALS; PRETREATMENT OF RAW MATERIALS
    • C22B5/00General methods of reducing to metals
    • C22B5/02Dry methods smelting of sulfides or formation of mattes
    • C22B5/12Dry methods smelting of sulfides or formation of mattes by gases
    • CCHEMISTRY; METALLURGY
    • C21METALLURGY OF IRON
    • C21BMANUFACTURE OF IRON OR STEEL
    • C21B13/00Making spongy iron or liquid steel, by direct processes
    • C21B13/0073Selection or treatment of the reducing gases
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10JPRODUCTION OF PRODUCER GAS, WATER-GAS, SYNTHESIS GAS FROM SOLID CARBONACEOUS MATERIAL, OR MIXTURES CONTAINING THESE GASES; CARBURETTING AIR OR OTHER GASES
    • C10J3/00Production of combustible gases containing carbon monoxide from solid carbonaceous fuels
    • C10J3/72Other features
    • C10J3/723Controlling or regulating the gasification process
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10KPURIFYING OR MODIFYING THE CHEMICAL COMPOSITION OF COMBUSTIBLE GASES CONTAINING CARBON MONOXIDE
    • C10K1/00Purifying combustible gases containing carbon monoxide
    • C10K1/002Removal of contaminants
    • C10K1/003Removal of contaminants of acid contaminants, e.g. acid gas removal
    • C10K1/005Carbon dioxide
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10KPURIFYING OR MODIFYING THE CHEMICAL COMPOSITION OF COMBUSTIBLE GASES CONTAINING CARBON MONOXIDE
    • C10K1/00Purifying combustible gases containing carbon monoxide
    • C10K1/04Purifying combustible gases containing carbon monoxide by cooling to condense non-gaseous materials
    • C10K1/046Reducing the tar content
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10KPURIFYING OR MODIFYING THE CHEMICAL COMPOSITION OF COMBUSTIBLE GASES CONTAINING CARBON MONOXIDE
    • C10K3/00Modifying the chemical composition of combustible gases containing carbon monoxide to produce an improved fuel, e.g. one of different calorific value, which may be free from carbon monoxide
    • C10K3/02Modifying the chemical composition of combustible gases containing carbon monoxide to produce an improved fuel, e.g. one of different calorific value, which may be free from carbon monoxide by catalytic treatment
    • C10K3/04Modifying the chemical composition of combustible gases containing carbon monoxide to produce an improved fuel, e.g. one of different calorific value, which may be free from carbon monoxide by catalytic treatment reducing the carbon monoxide content, e.g. water-gas shift [WGS]
    • CCHEMISTRY; METALLURGY
    • C21METALLURGY OF IRON
    • C21BMANUFACTURE OF IRON OR STEEL
    • C21B13/00Making spongy iron or liquid steel, by direct processes
    • C21B13/004Making spongy iron or liquid steel, by direct processes in a continuous way by reduction from ores
    • CCHEMISTRY; METALLURGY
    • C21METALLURGY OF IRON
    • C21BMANUFACTURE OF IRON OR STEEL
    • C21B13/00Making spongy iron or liquid steel, by direct processes
    • C21B13/02Making spongy iron or liquid steel, by direct processes in shaft furnaces
    • CCHEMISTRY; METALLURGY
    • C23COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
    • C23CCOATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
    • C23C8/00Solid state diffusion of only non-metal elements into metallic material surfaces; Chemical surface treatment of metallic material by reaction of the surface with a reactive gas, leaving reaction products of surface material in the coating, e.g. conversion coatings, passivation of metals
    • C23C8/06Solid state diffusion of only non-metal elements into metallic material surfaces; Chemical surface treatment of metallic material by reaction of the surface with a reactive gas, leaving reaction products of surface material in the coating, e.g. conversion coatings, passivation of metals using gases
    • C23C8/08Solid state diffusion of only non-metal elements into metallic material surfaces; Chemical surface treatment of metallic material by reaction of the surface with a reactive gas, leaving reaction products of surface material in the coating, e.g. conversion coatings, passivation of metals using gases only one element being applied
    • C23C8/20Carburising
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10JPRODUCTION OF PRODUCER GAS, WATER-GAS, SYNTHESIS GAS FROM SOLID CARBONACEOUS MATERIAL, OR MIXTURES CONTAINING THESE GASES; CARBURETTING AIR OR OTHER GASES
    • C10J2300/00Details of gasification processes
    • C10J2300/16Integration of gasification processes with another plant or parts within the plant
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10JPRODUCTION OF PRODUCER GAS, WATER-GAS, SYNTHESIS GAS FROM SOLID CARBONACEOUS MATERIAL, OR MIXTURES CONTAINING THESE GASES; CARBURETTING AIR OR OTHER GASES
    • C10J2300/00Details of gasification processes
    • C10J2300/18Details of the gasification process, e.g. loops, autothermal operation
    • C10J2300/1861Heat exchange between at least two process streams
    • C10J2300/1892Heat exchange between at least two process streams with one stream being water/steam
    • CCHEMISTRY; METALLURGY
    • C21METALLURGY OF IRON
    • C21BMANUFACTURE OF IRON OR STEEL
    • C21B2100/00Handling of exhaust gases produced during the manufacture of iron or steel
    • C21B2100/20Increasing the gas reduction potential of recycled exhaust gases
    • C21B2100/28Increasing the gas reduction potential of recycled exhaust gases by separation
    • C21B2100/282Increasing the gas reduction potential of recycled exhaust gases by separation of carbon dioxide
    • CCHEMISTRY; METALLURGY
    • C21METALLURGY OF IRON
    • C21BMANUFACTURE OF IRON OR STEEL
    • C21B2100/00Handling of exhaust gases produced during the manufacture of iron or steel
    • C21B2100/40Gas purification of exhaust gases to be recirculated or used in other metallurgical processes
    • C21B2100/44Removing particles, e.g. by scrubbing, dedusting
    • CCHEMISTRY; METALLURGY
    • C21METALLURGY OF IRON
    • C21BMANUFACTURE OF IRON OR STEEL
    • C21B2100/00Handling of exhaust gases produced during the manufacture of iron or steel
    • C21B2100/60Process control or energy utilisation in the manufacture of iron or steel
    • C21B2100/66Heat exchange
    • YGENERAL 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
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02PCLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
    • Y02P10/00Technologies related to metal processing
    • Y02P10/10Reduction of greenhouse gas [GHG] emissions
    • Y02P10/122Reduction of greenhouse gas [GHG] emissions by capturing or storing CO2
    • YGENERAL 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
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02PCLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
    • Y02P10/00Technologies related to metal processing
    • Y02P10/10Reduction of greenhouse gas [GHG] emissions
    • Y02P10/134Reduction of greenhouse gas [GHG] emissions by avoiding CO2, e.g. using hydrogen

Abstract

Method for producing steel, which comprises the steps of: providing a predetermined amount of iron ore to a vessel, reducing said iron ore to a predetermined amount of Fe, and carburizing said predetermined amount of Fe in order to produce steel. The steps of reducing and carburizing is performed using a main stream of CO and H2 being divided into at least two streams. In a first stream, H2 is removed from the stream and is fed to the vessel (9) for reducing said iron ore. A second stream comprising CO is fed to the vessel for carburizing said predetermined amount of Fe for producing steel with a predetermined content of C. The disclosure is also related to a system for producing steel according to the method.

Description

TECHNICAL FIELD The present disclosure relates to a method for producing steel according to claim 1 and to a system for producing steel according to claim BACKGROUND ART The conventional way of producing steel from iron ore requires a large amount of carbon rich coke to melt, reduce and carburize the steel. The steel industry is therefore one of the largest CO2 polluters in the world. lt is therefore of utmost importance to reduce the CO2 ppllution from steel production. To this fact it has been suggested to instead of using coke, it is possible to use hydrogen. See for example the document GB2112019A discussing such a method where the iron is reduced out from the iron ore.
SUMMARY OF THE INVENTION There is a need to provide steel out of the reduced iron ore.
An object of the present disclosure is to provide a method for producing steel wherein some of the problems with prior art technologies are mitigated or at least alleviated.
The disclosure proposes a method for producing steel. The method comprises the steps of: providing a predetermined amount of iron ore to a vessel, reducing the iron ore to a predetermined amount of Fe and carburizing the predetermined amount of Fe in order to produce steel. The steps of reducing and carburizing is performed using a main stream of CO and H2 being divided into at least two streams. ln a first stream, H2 is removed from the stream and is fed to the vessel for reducing the iron ore. A second stream comprising CO is fed to the vessel for carburizing the predetermined amount of Fe for producing steel with a predetermined content of C.
The advantage of the method is that the carbon content in the resulting steel is controlled in an accurate and reliable way by controlling the amount of CO and H2 in the first and second stream, respectively to a vessel to which iron ore is fed. No coke or methane is used upon reduction and carburization of the steel. Thus, the method provides for an environmentally friendly way of producing steel (so-called green steel) since very small amounts of C02 is formed in the vessel. Much less CO2 is formed upon production of the steel according to the present method as compared to the conventional steel production process. ln the conventionalprocess, more than 800 kg C02/ton iron ore is produced to be compared with about 450 kg C02 per 1000 kg iron ore of the present method. ln addition, the C02 formed in the present process is not formed in the vessel, instead it is formed in the process where it is co||ected thereby preventing C02 emission to the atmosphere. Thus, the proposed method is environmental friendly as compared With conventional steel production.
According to a further development, the amount of the second stream being fed to the vessel is controlled such that all carbon atoms from C0 of the second stream are bonded to Fe atoms when carburizing the predetermined amount of Fe.
The advantage is that a reliable and accurate way of producing steel with a predetermined content of C is provided.
According to a further development, the predetermined amount of Fe is carburized according the following formula, 3Fe+C0+H2=>Fe3C+H The carbon content in the steel is in the range of 0.0002 % to 10 %, preferably in the range of 0.002 % to 6.5 %, most preferably in the range of 0.02 to 2.5 %.
The advantage is that the carbon content of the steel is controlled.
According to a further development, the main stream of CO and H2 originates from syngas.
The advantage is that by using syngas upon producing steel according the present method very small amounts of C02 is formed in the vessel as compared to conventional steel production where coke for reducing and carburizing. By using syngas, the predetermined content of C in the steel is reliably and accurately controlled.
According to a further development, the syngas is extracted from waste, such as auto shredder residue, ASR, carbon fibre reinforced plastics, glass fibre reinforced plastics, sewage sludge, and/or municipal solid waste, MSW.
The advantage is that the energy bound in the waste is recovered. Furthermore, landfill which typically is the endpoint of many types of waste is reduced. Materials, such as metals, from the waste may be separated and recycled after formation of the syngas. By using waste for extraction of syngas, the method is very cost efficient.
According to a further development, the syngas is formed by allowing the waste to be heated to a temperature of at least 3000 °C. 3 The advantage is that syngas may be extracted from waste without the need of separating different parts of the waste, such as cabling and car upholstery of auto shredder residue, prior to recycling the different parts.
According to a further development, heat generated at the formation of syngas is used upon the steps of reducing and carburizing, such as for heating the vessel prior to or upon reducing the iron ore and/or carburizing of the Fe.
The advantage is that heat generated upon the formation of the syngas may be recovered upon production of the steel, such as for heating the vessel. The heat may also be recovered and used for heating other arrangements, such as buildings.
According to a further development, the syngas is subject to at least one cleaning step prior to forming the main stream of CO and H The advantage is that by cleaning the syngas, syngas having a high purity is formed. Thereby, the control of the predetermined amount of C in the steel becomes very reliable and accurate.
According to a further development, the step of reducing the iron ore to a predetermined amount of Fe, takes place according to the following formulas, 3Fe2O3 + H2 => 2Fe3O4 + H20, Fe3O4 + H2 => 3FeO + H20, and FeO + H2 => Fe + H2O.
The advantage by using H2 for reducing of the iron ore is that only Fe and H20 is formed. Thus, the proposed method is very environmentally friendly as compared to conventional methods for producing steel in which a large amount of C02 is formed upon reduction of the iron ore.
According to a further development, in the first stream the H2 is removed from the stream according to the following formula, CO + H2O => H2 + CO The advantage is that a high yield of H2 is removed from the first stream of H2 and CO in a very efficient way.
According to a further development, the method further comprises a step of separating the CO2 and H2 and collecting the CO2 in a sealed container.This provides for improved handling of the C02 formed by the proposed method as compared to conventional production of steel where C02 is formed in the vessel. The advantage is that C02 formed upon removing of H2 in the first stream, is co||ected in a sea|ed container thereby preventing emission of C02 to the atmosphere. The separated C02 may be subject to carbon capture and utilization, CCU, where the C02 is recycled.
According to a further development, in the step of providing a predetermined amount of iron ore to a vessel also a predetermined amount of scrap iron is provided to the vesseL This provides for that scrap iron is recycled and is used in the process for producing steel. By the use of scrap iron, a smaller amount of iron ore is used, thereby the process becomes more energy efficient and cost efficient.
The disclosure further proposes a system for producing steel according to the method. The system comprises at least one vessel. The vessel comprises an inlet for iron ore, an inlet for H2 and one inlet for C0 + H2 and an outlet for produced steel with a predetermined carbon content.
The system is able to produce steel according to the proposed method. Thus, the system provides for production of steel having all the above-mentioned advantages. ln addition, the system may be modular comprising a number of units, thus the system may be designed and redesigned depending on the needs of the steel producer.
BRIEF DESCRIPTION OF THE DRAWINGS Fig. 1 schematically illustrates an example of a system for producing steel according to the method of the present disclosure.
Fig. 2 illustrates the method according to the present disclosure.
DETAILED DESCRIPTION The present disclosure relates to a method for producing steel.
Fig. 1 schematically illustrates an example of a system 100 for producing steel according to the method of the present disclosure.The system 100 may be modular and comprises a number of different units which will be described more in detail below. The modularity of the system 100 may facilitate design and redesign of the system 100. The system 100 may be tailor-made for example depending on type and size of a feedstock being fed into the system. Standard conduits for liquids and gases may be used for connecting the different units of the system 100 to each other.
The system 100 comprises at least one vessel 9 comprising an inlet 15 for iron ore, an inlet 17 for H2 and one inlet 18 for CO + H2 and an outlet 16 for produced steel with a predetermined carbon content.
The system 100 may further comprise a water-gas-shift unit 7, a pressure swing adsorption (PSA) unit 8, at least one valve 14a, 14b and a control unit 10. The system may further comprise a cleaning unit 6, a heat recovery unit 4, a container for inorganic material 5, a gasification unit 2, a container for slug collection 3, an oxygen generator 12, a chopper/shredder unit 1, a container for collecting C02 11, and/or a pump system As illustrated in Fig. 1, the system may comprise a chopper/shredder unit 1 to which a feedstock, i.e. a raw material, is provided. The chopper/shredder unit 1 is arranged for chopping/shredding the feedstock into a desired size. The system may comprise a plurality of chopper/shredder units 1. The size and type of the chopper/shredder unit 1 chosen may depend on the size and type of feedstock the system is arranged to process. ln a further example, the feedstock is provided in a desired size and/or shape prior to entering the system 100 and a chopper/shredder unit 1 is not needed. ln such case, the feedstock may be directly fed into a gasification unit 2, which will be described in detail below.
The feedstock may comprise waste, such as auto shredder residue, ASR, carbon fibre reinforced plastics, glass fibre reinforced plastics, sewage sludge and/or municipal solid waste, MSW. The feedstock may comprise other types of organic materials and/or inorganic materials, such as metals. Typically, the feedstock comprises a mix of organic and inorganic materials. ln one example, the feedstock comprises very large objects, such as wind blades from wind turbines and hulls from plastic boats. ln another example, the feedstock comprises parts from car interiors, such as car upholstery, car dashboards and cablings.The system may comprise a gasification unit 2. The system 100 may further comprise a feeding unit (not shown) for feeding the feedstock into a gasification unit 2. The feeding unit may for example be a screw arrangement.
The gasification unit 2 may comprise a pyrolysis zone and a plasma zone. The pyrolysis zone may be arranged for combusting of the feedstock in presence of a predetermined amount of oxygen. The oxygen may be provided from an oxygen generator 12. The oxygen generator 12 may comprise a pressure swing adsorption (PSA) unit and a compressor. The amount of oxygen provided may be controlled manually or automatically by means of a valve (not shown). The amount of oxygen provided and the temperature upon combustion may depend on the desired degree of combustion of the feedstock. The temperature upon combustion of the feedstock, i.e. in the pyrolysis zone, may be in the range of about 600 to 900 °C. The combusted feedstock, i.e. ash, may then be provided to the plasma zone of the gasification unit 2. The plasma zone of the gasification unit 2 may be heated to a temperature of at least 3000 °C. The plasma zone may comprise a light arc in which the formation into plasma of the combusted feedstock takes place. Due to the very high temperature, the chemical bonds of the compounds of the combusted feedstock are broken and the compounds may be decomposed into a plasma. 0xygen may be provided by the oxygen generator to the plasma zone in order to form CO of carbon being released upon the formation of plasma. The plasma formed in the gasification unit 2 comprises syngas. By providing pure oxygen instead of air, it is avoided that the resulting syngas comprises unnecessarily high amounts nitrogen or nitrogen compounds.
Syngas, also known as synthesis gas, is a gas mixture comprising primarily of H2 and CO. Depending on the process in which the syngas is formed, such as the material of the feedstock and temperatures in the pyrolysis zone and the plasma zones of the gasification unit 2. The syngas may also comprise small amounts of other gases, such as H20, C02, N2 and CH4. As an example, cooled syngas may comprise about 5 % N2 and about 5 % C02. Before being cooled, the syngas may also comprise up to 25 % of H Upon formation of the syngas, there may also be some residual materials formed in the gasification unit 2, such as inorganic materials, which is condensed before the gas is leaving the plasma zone or is not fully decomposed into plasma. These materials may be collected in a slag collection unit 3. The materials collected in the slag collection unit 3 are typically materials having a relatively high boiling point. Examples of such materials are metals, such as copper (Cu), and silicon (Si). The materialscollected in the slag collection unit 3 may be recycled and reused in manufacturing industry.
The system 100 may comprise more than one gasification unit 2 in order to ensure a high utilization of material of the feedstock.
The system 100 may further comprise a heat recovery unit 4. The heat recovery unitis arranged to cool the syngas being formed in the gasification unit ln the heat recovery unit 4, the syngas may be cooled by a working fluid, such as water. The working f|uid may be arranged to circu|ate in a closed system 19 by means of a pump system 13. The heating f|uid may be circulated to different units of the system 100, thereby heating and/or cooling different units of the system 100. ln one example (shown in Fig. 1), the closed system may be arranged to circu|ate the working liquid from the heat recovery unit 4 to a water-gas-shift unit 7, to a vessel 9 and back to the heat recovery unit 4. Typically, heat is generated in the recovery unitand/or in the water-gas-shift unit As will be discussed more in detail below, heat generated in the heat recovery unit 4 and/or in the water-gas-shift unit 7 may be used to heat the vessel 9 upon reducing and carburizing. For example, the heat may be used for pre-heating of the iron ore in the vessel 9. Alternatively, the heat generated in the recovery unit 4 and/or in the water-gas-shift unit 7 may be used for heating other arrangements.
Upon cooling of the syngas, condensed inorganic materials may be collected in a container 5. The materials collected in the container 5 is typically materials having a boiling point which is lower than the boiling point of the materials being collected in the slag collection unit 3. Examples of materials being collected in the container 5 is aluminum and cadmium. The materials collected in the container 5 may be recycled and reused in manufacturing industry.
The system may further comprise a cleaning unit 6. The cleaning unit 6 is arranged for cleaning and purifying of the syngas. ln one example, the syngas may be led from the heat recovery unit 4 to the cleaning unit 6 by means of a fan device (not shown).
The cleaning unit 6 may comprise filters and/or a cleaning liquid which is circulated in the cleaning unit 6 by means of a pump system. ln one example, the syngas is firstly led through one or more filters in order to purify the syngas from undesired compounds. Secondly, the syngas is “showered” by the cleaning liquid. The cleaning liquid may typically be water. ln this step, H20 and water-soluble compounds may beseparated from the syngas. The syngas may be repeatedly circulated within the cleaning unit 6 until the syngas has reached a desired purity.
The system 100 may comprise a plurality of cleaning units 6 arranged after one another. ln one example, the plurality of cleaning units 6 may comprise different types of filters and/or cleaning liquids. The syngas resulting from the cleaning unit 6 typically comprises H2 and CO in the ratio of 1:1. ln addition, the syngas may comprise small amounts of CO2, N2 and traces of CH The syngas resulting from the cleaning unit 6 may, but need not, be compressed by a compressor (not shown).
The system 100 may further comprise at least one valve 14a, 14b. ln one example, the at least one valve 14a may be arranged for controlling the amount of H2 and CO being divided into the first stream and at least one valve 14b is arranged for controlling the amount of H2 and CO being divided into the second stream. ln one example, the at least one valve 14a, 14b is manually controlled by an operator. ln yet an example, the system may comprise a control unit 10 which may be arranged to control the at least one valve 14a, 14b automatically.
The control unit 10 may be arranged to control the at least one valve based on a predetermined carbon content of the steel. ln one example, the control unit 10 may be arranged to divide the main stream into 30 % to the second stream and the remaining 70 % to the first stream.
The main stream of syngas may have been formed in the gasification unit 2 and may, as described above, have been subject to cooling in the heat recovery unit 4 and/or cleaning in the cleaning unit 6. ln a first stream, H2 is removed from the stream and is fed to the vessel (9) for reducing said iron ore. The second stream comprising of CO and H2 is fed to the vessel 9 for carburizing the predetermined mount of Fe.
The system 100 may further comprise a water-gas-shift unit 7, to which the first stream of CO and H2 (syngas) is fed. The water-gas-shift unit 7 is arranged for removing CO from the first stream. ln the water-gas-shift unit 7, water steam is provided, wherein CO from the syngas reacts with water, thereby forming CO2 and H2. The water-gas-shift unit 7 may be a commercial available water-gas-shift unit. As discussed above, the water-gas-shift unit 7 may generate heat which may be arranged to heat the working liquid in the closed loopThe system 100 may further comprise a pressure swing adsorption, PSA, unit 8. Pressure swing adsorption is a well-known technique used to separate some gas species from a mixture of gases. ln the system 100, the pressure swing adsorption unit 8 is arranged for separating C02 and H2. The resulting H2 being separated by the swing adsorption unit 8 has a high purity, typically in the range of 99.999 %.
The C02 being separated in the PSA unit 8 may preferably be liquefied and be stored in a sealed container 11. The separated C02 may be subject to carbon capture and utilization, CCU. CCU is a process where carbon dioxide is captured and is recyc|ed for further usage. The aim of CCU is to convert the captured carbon dioxide into e.g. plastics, concrete or biofue| in a controlled way, thereby preventing the C02 from reaching the atmosphere. Alternatively, the C02 may be subject to carbon capture and storage, CCS, wherein the C02 may be permanently stored in an underground geo|ogica| formation, thereby preventing the C02 from reaching the atmosphere.
The system further comprises at least one vessel 9. The vessel 9 comprises an inlet for iron ore 15, an inlet for H2 17, and one inlet for C0 + H2 18 and an outlet for produced steel 16 with a predetermined carbon content.
The vessel 9 is arranged for reducing iron ore (iron oxides) and for carburization of iron into steel. The vessel 9 may be a commercial available MlDREX® shaft furnace. lron ore is provided to an inlet 15, which typically is arranged at the top of the vessel 9. The iron ore descends downwards in the vessel 9 due to gravity wherein the iron ore is reduced to a predetermined amount of Fe and a predetermined amount of Fe is carburized in order to produce steel.
As mentioned above, the resulting H2 being removed from the first stream is fed into the vessel 9 for reducing the iron ore. The H2 is fed to the vessel via the inlet 17. A second stream comprising C0 and H2 is fed to the vessel 9 for carburizing the predetermined mount of Fe. The second stream is fed to the vessel via inlet 18. Upon reducing the iron ore and carburizing the predetermined amount of Fe, the vessel 9 may be heated to a temperature of about 1500 °C. Details regarding the reduction of iron ore and carburization of Fe are discussed in detail with reference to the method below. As shown in Fig. 1, the resulting steel is output from the outlet 16, which typically is arranged at the lower end of the vessel As mentioned above, and being illustrated in Fig. 1, the heat circulating in a closed loop 19 from the heat recovery unit 4 and/or the water-gas-shift unit 7 may be used for heating the vessel 9, upon the steps of reducing and carburizing. ln one example, the working liquid in the closed loop 19 may be used for heating the vessel 9 prior to or upon reducing the iron ore and/or carburizing of the Fe.
The system described above may be used for the method of producing steel according to the present disclosure. Fig. 2 schematically i||ustrated the method according to the present disclosure.
The method for producing steel comprises a step of providing a predetermined amount of iron ore to a vessel 9. lron ores comprises rocks and minerals from which metallic iron may be extracted. The iron ore typically comprises different types of iron oxides, such as magnetite (Fe3O4), hematite (FezOs) and FeO (wüstite). By “predetermined amount” is meant the amount of iron ore from which it is desired to extract iron. ln the step of providing a predetermined amount of iron ore to a vessel also a predetermined amount of scrap iron may be provided to the vessel 9. By scrap iron is meant for example parts of steel from scrapped vehicles.
The method further comprises a step of reducing said iron ore to a predetermined amount of Fe. ln the step of reducing the iron ore, oxygen is removed from the iron ore. By reduction is meant the gain of electrons or decrease in the oxidation state of an atom, an ion or of certain atoms in a molecule. As will be discussed more in detail below, H2 is used for reducing the iron ore in the method of the present disclosure. By “predetermined amount” is meant the amount of iron which is desired to be carburized in order to produce steel.
The method further comprises a step of carburizing said predetermined amount of Fe in order to produce steel. By carburizing is meant that Fe or steel absorbs carbon while the Fe is heated in the presence of a high carbon content material. The reason for carburizing the iron is to provide steel with desired properties, such as a desired hardness of the steel. Thus, by controlling the carbon content in the resulting steel, the hardness of the resulting steel is controlled.
The steps of reducing and carburizing is performed using a main stream of CO and H2. The main stream of CO and H2 may be syngas.
The syngas may be extracted from waste, such as auto shredder residue, ASR, carbon fibre reinforced plastics, glass fibre reinforced plastics, sewage sludge, and/or municipal solid waste, MSW. The formation of syngas from waste was discussed in detail above with reference to the system.The main stream of CO and H2 is divided into at least two streams. ln a first stream, H2 is removed from the stream and is fed to the vessel 9 for reducing said iron ore. A second stream is fed to the vessel 9 for carburizing the predetermined amount of Fe for producing steel with a predetermined amount of C. The ratio of CO to H2 is typically 1:1 in the main stream as well as in the first and second streams.
As described with reference to the system above, the amount of the main stream of CO and H2 being divided into the at least two streams is controlled by the control unit 10. Alternatively, the amount of the main stream of CO and H2 being divided into the at least two streams is manually controlled by at least one valve 14a, 14b. The ratio of the first and the second stream is controlled based on the amount of carbon from the CO needed in order to produce steel with a predetermined content of C.
The amount of the second stream being fed to the vessel may be controlled such that all carbon atoms from CO of the second stream are bonded to Fe atoms when carburizing the predetermined amount of Fe. lf there is an excess of CO and/or carbon atoms in the second stream not all of the carbon atoms may be bonded to Fe. Thus, an excess of CO may result in an undesired high carbon content of the steel and/or formation of undesired CO2 in the vessel.
The amount of compressed H2 and CO (syngas) needed for reducing and carburizing 1000 kg of iron ore (Fe2O3) is in the range of 10-50 kg, depending on the amount of the desired carbon content in the resulting steel. ln one example, 25 kg H2 and CO (syngas) results in a carbon content in the steel of about 1 %.
The remaining portion of the main stream may then be provided into the first stream. Alternatively, also the amount of the main stream being divided into the second stream is controlled. The amount of H2 and CO (syngas) in the first stream needs to be high enough to produce an amount of resulting H2 needed to reduce the carbon ore into a predetermined amount of Fe in the vessel. However, an excess of H2 in the vessel upon reducing of the iron ore as well as upon carburization does not affect the carbon content in the steel. Thus, an excess of H2 in the vessel does not adversely affect the production of the steel. ln a first stream, H2 is removed from the stream and is fed to the vessel 9 for reducing said iron ore. The H2 may be removed from the stream by means of a water-gas-shift unit as described with reference to the system above. The H2 may be removed according to the following formula, CO + H2O => H2 + COAs described above, the CO2 may be separated from the H2 by means of a pressure swing adsorption unit, PSA unit, and may be collected in a sealed container.
The step of reducing the iron ore to a predetermined amount of Fe may take place according to the following formulas, 3Fe2O3 + H2 => 2Fe3O4 + H2O Exothermic reaction FesO4 + H2 => 3FeO + H2O, and Endothermic reaction FeO + H2 => Fe + H20 Endothermic reaction Thus, upon the step of reducing the iron ore, a predetermined amount of Fe is formed. As will be described more in detail below, the resulting predetermined amount of Fe is carburized in order to produce steel. As noted above, H2O formed during the reducing of iron ore. The H2O vaporizes due to the high temperature in the vessel. Typically the vaporized H2O is may be led out via a chimney (not shown) which is arranged on the vessel. The heat from the vaporized H2O may also be recovered and used for heating purposes.
The second stream is fed to the vessel for carburizing said predetermined amount of Fe for producing steel with a predetermined content of C.
The amount of the second stream being fed to the vessel is controlled such that all carbon atoms from CO of the second stream are bonded to Fe atoms when carburizing said predetermined amount of Fe. As described above with reference to the system, the control of the amount of the main stream being divided into the first stream and the second stream may be performed by the control unit. An excess of CO may result in an undesired high C content in the steel and/or undesired formation of CO2 in the vessel. The predetermined amount of Fe may be carburized according the following formula, 3Fe + CO + H2 => Fe3C + H2O.
The carbon content in the steel may be in the range of 0.0002 % to 10 %, preferably in the range of 0.002 % to 6.5 %, most preferably in the range of 0.02 to 2.5 %.
The amount of H2 and CO of the first and second stream, respectively, is determined depending on the desired properties of the resulting steel, such as the desired hardness of the resulting steel. The properties of the steel depends on the amount of carbon bonded to the Fe atoms in the steel. An increased amount of CO provided tothe predetermined amount of Fe, thus results in an increased percentage of carbon in the steel. Typically, the amount of CO and H2 that is needed for the desired carbon content in the steel is provided for the carburizing (second stream) and then the remaining amount of CO and H2 is divided into the first stream in which the H2 is removed from the stream and fed to the vessel. The amount of CO needed in order to carburize the iron depends on the amount of iron ore provided to the vessel. ln one example, 70 % of the CO and H2 is provided in the first stream and 30 % of the CO and H2 is provided in the second stream. By this method, all carbon atoms in the steel originates from CO.
Conventional method for production of steel for comparison Production of steel typically results in formation of large amounts of carbon dioxide. The conventional reduction process of iron ore (iron oxides) typically takes place by carbon monoxide from coke according to the following chemical reactions below: 3Fe2 Og + CO => 2Fe3O4 + CO2 Exothermic reaction Fe3O4 + CO => 3FeO + CO2 Endothermic reaction FeO + CO => Fe + CO2 Exothermic reaction Further, conventional carburization of iron takes place according to the following reaction: 3Fe + 2CO => FegC + CO2 Exothermic reaction As seen above, carbon dioxide is formed during both the reduction and carburization steps upon the conventional method for producing steel.

Claims (1)

  1. CLAIMS Method for producing steel (200), which comprises the steps of: providing (210) a predetermined amount of iron ore to a vesse| (9), reducing (220) said iron ore to a predetermined amount of Fe, carburizing (230) said predetermined amount of Fe in order to produce steel, wherein the steps of reducing and carburizing is performed using a main stream of CO and H2 being divided into at least two streams, wherein in a first stream H2 is removed from the stream and is fed to the vesse| (9) for reducing said iron ore, and a second stream comprising CO is fed to the vesse| (9) for carburizing said predetermined amount of Fe for producing steel with a predetermined content of C. _ The method (200) according to claim 1,wherein the amount of the second stream being fed to the vesse| is controlled such that all carbon atoms from CO of the second stream are bonded to Fe atoms when carburizing said predetermined amount of Fe. The method (200) according to claim any of the preceding claims, wherein the predetermined amount of Fe is carburized according the following formula, 3F6+CO+H2=>F63C+H2O, wherein carbon content in the steel is in the range of 0_0002 % to 10 %, preferably in the range of 0.002 % to 6.5 %, most preferably in the range of 0.02 to 2.5 %_ _ The method (200) according to any of the preceding claims, wherein the main stream of CO and H2 originates from syngas. The method (200) according to claim 4, wherein said syngas is extracted from waste, such as auto shredder residue, ASR, carbon fibre reinforced plastics, glass fibre reinforced plastics, sewage sludge, and/or municipal solid waste, MSW. _ The method (200) according to claim 5, wherein said syngas is formed by allowing the waste to be heated to a temperature of at least 3000 °C__ The method (200) according to claim 6, wherein heat generated at the formation of syngas is used upon the steps of reducing and carburizing, such as for heating the vessel prior to or upon reducing the iron ore and/or carburizing of the Fe. _ The method (200) according to claim any of claims 4 to 7, wherein the syngas is subject to at least one c|eaning step prior to forming the main stream of CO and H The method (200) according to any of the preceding claims, wherein the step of reducing the iron ore to a predetermined amount of Fe, takes place according to the following formulas, 3FG2Û3 + H2 => 2FG3Û4 + H2O, FG3Û4 + H2 => 3FGO + H2Û, and FeO + H2 => Fe + H The method (200) according to any of the preceding claims, wherein in the first stream the H2 is removed from the stream according to the following formula, CO + H2O => H2 + CO .The method (200) according to claim 10, further comprising a step of separating the CO2 and H2 and collecting the CO2 in a sealed container. 12.The method (200) according to any of the preceding claims, wherein in the step of providing (210) a predetermined amount of iron ore to a vessel (9) also a predetermined amount of scrap iron is provided to the vessel (9). 13.System (100) for producing steel comprising at least one vessel (9) comprising an inlet (15) for iron ore, an inlet for H2 (17) and one inlet for CO + H2 (18) and an outlet (16) for produced steel with a predetermined carbon content, wherein said system is arranged for producing steel according to the method of any of claims 1-12.
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US7854786B2 (en) * 2006-01-31 2010-12-21 Danieli & C. Officine Meccaniche S.P.A. Reduction process and plant
DE202021001452U1 (en) * 2021-04-20 2021-05-26 EAT Anlagenbau UG (haftungsbeschränkt) Plant for the production of fluid fuels
US20210246521A1 (en) * 2018-06-12 2021-08-12 Primetals Technologies Austria GmbH Method for Carburization of HDRI produced in H2 based Direct Reduction Process

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GB2112019A (en) 1981-12-18 1983-07-13 British Steel Corp Reduction of agglomerated iron ore
US10316376B2 (en) * 2015-06-24 2019-06-11 Midrex Technologies, Inc. Methods and systems for increasing the carbon content of sponge iron in a reduction furnace

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US7854786B2 (en) * 2006-01-31 2010-12-21 Danieli & C. Officine Meccaniche S.P.A. Reduction process and plant
US20210246521A1 (en) * 2018-06-12 2021-08-12 Primetals Technologies Austria GmbH Method for Carburization of HDRI produced in H2 based Direct Reduction Process
DE202021001452U1 (en) * 2021-04-20 2021-05-26 EAT Anlagenbau UG (haftungsbeschränkt) Plant for the production of fluid fuels

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