Classifications

• • C—CHEMISTRY; METALLURGY
  • C21—METALLURGY OF IRON
  • C21C—PROCESSING OF PIG-IRON, e.g. REFINING, MANUFACTURE OF WROUGHT-IRON OR STEEL; TREATMENT IN MOLTEN STATE OF FERROUS ALLOYS
  • C21C7/00—Treating molten ferrous alloys, e.g. steel, not covered by groups C21C1/00 - C21C5/00
  • C21C7/04—Removing impurities by adding a treating agent
  • C21C7/068—Decarburising
• • C—CHEMISTRY; METALLURGY
  • C21—METALLURGY OF IRON
  • C21C—PROCESSING OF PIG-IRON, e.g. REFINING, MANUFACTURE OF WROUGHT-IRON OR STEEL; TREATMENT IN MOLTEN STATE OF FERROUS ALLOYS
  • C21C1/00—Refining of pig-iron; Cast iron
  • C21C1/04—Removing impurities other than carbon, phosphorus or sulfur
• • C—CHEMISTRY; METALLURGY
  • C21—METALLURGY OF IRON
  • C21C—PROCESSING OF PIG-IRON, e.g. REFINING, MANUFACTURE OF WROUGHT-IRON OR STEEL; TREATMENT IN MOLTEN STATE OF FERROUS ALLOYS
  • C21C5/00—Manufacture of carbon-steel, e.g. plain mild steel, medium carbon steel or cast steel or stainless steel
  • C21C5/28—Manufacture of steel in the converter
• • C—CHEMISTRY; METALLURGY
  • C21—METALLURGY OF IRON
  • C21C—PROCESSING OF PIG-IRON, e.g. REFINING, MANUFACTURE OF WROUGHT-IRON OR STEEL; TREATMENT IN MOLTEN STATE OF FERROUS ALLOYS
  • C21C5/00—Manufacture of carbon-steel, e.g. plain mild steel, medium carbon steel or cast steel or stainless steel
  • C21C5/28—Manufacture of steel in the converter
  • C21C5/30—Regulating or controlling the blowing
  • C21C5/35—Blowing from above and through the bath
• • C—CHEMISTRY; METALLURGY
  • C21—METALLURGY OF IRON
  • C21C—PROCESSING OF PIG-IRON, e.g. REFINING, MANUFACTURE OF WROUGHT-IRON OR STEEL; TREATMENT IN MOLTEN STATE OF FERROUS ALLOYS
  • C21C7/00—Treating molten ferrous alloys, e.g. steel, not covered by groups C21C1/00 - C21C5/00
  • C21C7/04—Removing impurities by adding a treating agent
  • C21C7/072—Treatment with gases
• • C—CHEMISTRY; METALLURGY
  • C21—METALLURGY OF IRON
  • C21C—PROCESSING OF PIG-IRON, e.g. REFINING, MANUFACTURE OF WROUGHT-IRON OR STEEL; TREATMENT IN MOLTEN STATE OF FERROUS ALLOYS
  • C21C7/00—Treating molten ferrous alloys, e.g. steel, not covered by groups C21C1/00 - C21C5/00
  • C21C7/10—Handling in a vacuum

Definitions

• the present invention relates to a method that obtains molten steel by decarburizing untreated molten iron with a carbon concentration of 3.0 mass% or lower to reduce the nitrogen concentration in the decarburized molten iron, and thereby obtain low-nitrogen steel.
• this method is suitable for a case in which part or the whole of the untreated molten iron is obtained by melting a cold iron source.
• the nitrogen concentration at the time of discharging the molten steel can be high compared with when refining molten pig iron discharged from a blast furnace, which is hereinafter referred to as "blast furnace molten pig iron", in a converter and discharging the molten steel.
• blast furnace molten pig iron refining molten pig iron discharged from a blast furnace
• nitrogen is removed mainly by having it adsorbed onto bubbles of carbon monoxide that are generated by decarburization, so that the nitrogen concentration at the time of discharging the molten steel is generally low.
• blast-furnace molten pig iron contains about 4 mass% carbon, and the amount of carbon monoxide generated by decarburization refining is large enough to allow smelting of low-nitrogen steel with a nitrogen concentration of about 20 mass ppm.
• the carbon concentration in molten iron resulting from melting the cold iron source is low and the amount of carbon monoxide to be generated is limited, which makes it difficult to remove nitrogen to a low concentration. It is possible to denitrify the molten iron resulting from melting a cold iron source to some extent by subjecting it to a vacuum degassing treatment or the like.
• the upper limit of the nitrogen concentration at which stable smelting is possible is about 40 mass ppm.
• reduced iron contains 0.5 mass% to 2.0 mass% carbon. Therefore, molten iron obtained by melting such reduced iron requires decarburization refining, during which it can be denitrified to some extent. From the viewpoint of increasing the amount of nitrogen to be removed, it is conceivable to increase the carbon concentration in molten iron resulting from melting reduced iron in an electric furnace etc. by, for example, mixing this molten iron with blast-furnace molten pig iron, and then perform decarburization refining in a converter. In the future, however, to reduce CO 2 generation, the amount of blast-furnace molten pig iron produced is likely to decrease and the amount of cold iron source used is likely to increase. Then, the carbon concentration at the time of charging into a converter is expected to become lower, which would make it difficult to sufficiently reduce the nitrogen concentration at the time of discharging the molten steel.
• Patent Literature 1 proposes a method in which molten steel discharged from a converter is recarburized and deoxidized with Al, and then oxygen is blown during a vacuum degassing treatment to perform decarburization refining.
• the N concentration [N] in the molten steel is reduced to 25 mass ppm or lower.
• Patent Literature 2 proposes a molten steel denitrification method in which CaO is fed onto a bath surface of molten steel without recarburization, then an Al-containing substance is added to remove nitrogen from the molten steel into slag as nitride, and further oxygen is blown to remove nitrogen into a gas phase as a nitrogen gas.
• the nitrogen concentration is reduced to 20 mass ppm or lower.
• Patent Literature 3 proposes a vacuum refining method in which, in an RH vacuum degassing treatment device, a hydrocarbon gas is supplied as a circulating gas to be supplied through an immersion pipe to thereby break up bubbles.
• a hydrocarbon gas is supplied as a circulating gas to be supplied through an immersion pipe to thereby break up bubbles.
• the nitrogen concentration is reduced to 20 mass ppm or lower.
• Patent Literature 1 has a problem in that the amount of CO 2 generated increases as an extra carbon source is added to generate bubbles of carbon monoxide, and another problem in that the productivity decreases as performing decarburization again during the vacuum degassing treatment prolongs the treatment time.
• Patent Literature 2 requires adding at least 3 kg of metal Al per ton of molten steel, which leads to a significant cost increase. Moreover, after metal Al is added, Al in the molten steel needs to be removed again through oxidization. Thus, there are problems in that the productivity decreases due to the increased treatment time and that the amount of slag discharged increases.
• the present invention has been devised in view of these circumstances, and an object thereof is to propose a method for refining molten iron that stably produces low-nitrogen steel under the condition of an increased amount of cold iron source used, without causing a significant decrease in productivity or a cost increase, and without adding to the amount of slag generated or the amount of CO 2 generated.
• a method for refining molten iron according to the present invention that advantageously solves the above-described problems is a method in which untreated molten iron with a carbon concentration [C]i between 0.5 mass% and 3.0 mass%, both inclusive, is placed into a vessel, and oxygen is blown onto the untreated molten iron under atmospheric pressure while a hydrogen gas, a hydrocarbon gas, or a mixture gas of these gases is blown in to perform a decarburization and denitrification treatment of the untreated molten iron.
• the present invention makes it possible to stably produce low-nitrogen steel with a nitrogen concentration [N] ⁇ in treated molten steel of 30 mass ppm or lower under the condition of an increased amount of cold iron source used, without causing a significant decrease in productivity or a cost increase, and without adding to the amount of slag generated or the amount of CO 2 generated.
• an iron source is melted and heated using electric energy.
• an electric furnace such as an arc furnace or an induction furnace.
• the iron source not only a solid iron source, such as scrap or reduced iron, but also molten iron that has been melted by another process may be used.
• the heat energy supplied to melt the solid iron source and heat the iron source not only electric energy but also combustion heat of metal etc. may be supplementarily used. It is preferable that these energies be renewable energies from the viewpoint of cutting down on CO 2 emissions.
• the molten iron is discharged into a vessel, such as a ladle.
• a vessel such as a ladle.
• reduced iron is used as the cold iron source
• a large amount of slag attributable to gangue contained in the reduced iron is generated. Therefore, performing slag removal as necessary is desirable.
• Slag removal may be performed using a slag dragger or the like.
• the furnace body may be tilted to flow out the slag.
• the furnace body may be tilted to flow out the slag, and then the slag flown into a vessel, such as a ladle, along with the molten iron may be further removed.
• the molten iron is mixed with molten pig iron, such as blast-furnace molten pig iron, as necessary to adjust the carbon concentration [C]i in the molten iron to between 0.5 mass% and 3.0 mass%, both inclusive. Then, this molten iron is charged into a reaction vessel, and decarburization refining is performed by supplying an oxygen gas through a top-blowing lance etc.
• the carbon concentration [C]i in the untreated molten iron is lower than 0.5 mass%, denitrification may become insufficient due to the small amount of CO gas generated during decarburization.
• the carbon concentration exceeds 3.0 mass% the reducing effect on CO 2 generation lessens.
• the molten pig iron to be mixed is preferable to have a carbon concentration of 2.0 mass% or higher, and may be molten pig iron as discharged from a blast furnace, or may be molten pig iron that has undergone one of desiliconization, dephosphorization, and desulfurization or a combination of two or more of these treatments after being discharged from a blast furnace.
• a converter is preferable in terms of the height of the freeboard (the height from the upper end of the reaction vessel to the surface of the molten iron).
• the reaction vessel should be a vessel in which oxygen blowing is possible, and may also be a ladle or the like.
• Oxygen blowing is not limited to a method of supplying oxygen through a top-blowing lance, and oxygen may instead be supplied through a bottom-blowing tuyere.
• a combination of supplying oxygen through a top-blowing lance and supplying oxygen through a bottom-blowing tuyere may be adopted.
• a gas containing hydrogen atoms formed by a hydrogen gas or a hydrocarbon gas or a mixture gas of these gases is supplied through a porous plug etc. installed at the bottom of the furnace. It is believed that when a gas containing hydrogen atoms is supplied into molten iron, after a dissociation reaction of gas molecules occurs, hydrogen atoms dissolve temporarily into the molten iron and are then generated as fine hydrogen gas bubbles again. The denitrification reaction is believed to progress between the fine bubbles generated here and the molten iron interface.
• Nm 3 means a volume of a gas in a normal state. In this Description, the normal state of a gas is 0°C and 1 atm (101325 Pa).
• supply of the oxygen gas is stopped and, at the same time, supply of the gas containing hydrogen atoms is stopped.
• supply of the gas containing hydrogen atoms after it is stopped, be switched to supply of an inert gas, such as an argon gas.
• the gas containing hydrogen atoms is not limited to being supplied through a porous plug and may instead be supplied using an injection lance (immersion lance), a single pipe, or a double pipe.
• Performing a treatment such that the nitrogen concentration [N] ⁇ in the treated molten iron becomes 30 mass ppm or lower is preferable, because then low-nitrogen steel with a nitrogen concentration N in the product at the stage of crude steel, such as a steel slab, of 30 mass ppm or lower can be produced.
• Performing a treatment such that the nitrogen concentration [N] ⁇ in the treated molten iron becomes 20 mass ppm or lower through adjustment of the treatment conditions so as to increase the amount of hydrogen atoms supplied, for example, by increasing the flow rate of the hydrogen gas or by using a hydrocarbon-based gas containing a large amount of hydrogen per gas volume is further preferable, because this results in extremely low-nitrogen steel.
• a vacuum degassing treatment is performed, and casting is performed preferably after being otherwise adjusted to a predetermined composition.
• hydrogen can be removed.
• This embodiment can prevent a decrease in productivity compared with the technology described in Patent Literature 3 in which a gas containing hydrogen atoms is supplied in a vacuum degassing treatment.
• an RH vacuum treatment device, a DH vacuum treatment device, a facility with a ladle installed inside a vacuum chamber, etc. can be used.
• Scrap or reduced iron as a cold iron source was charged into a 150 t-scale electric furnace and melted. After the molten iron was discharged into a ladle, slag removal was performed. The reduced iron used in the test was reduced iron produced through reduction with a natural gas, and the carbon concentration was analyzed to be 1.0 mass%. The discharged molten iron inside the ladle and blast-furnace molten pig iron were mixed in a converter-charging pot so as to adjust the amount of molten iron to 300 t. After the components of the molten iron were analyzed, the molten iron was charged into a converter and subjected to decarburization blowing.
• the amount of carbon contained in the blast-furnace molten pig iron used as the molten metal to be mixed was 4.3 mass%.
• the mixing ratio between the molten iron obtained by melting a cold iron source and the blast-furnace molten pig iron were changed to various ratios, and the carbon concentration [C]i (mass%) at the time of charging into the converter was also changed to various concentrations.
• An oxygen gas needed for decarburization was supplied through a top-blowing lance, and the amount of oxygen gas to be supplied was determined based on analytical values (represented with a suffix "i") of carbon and others in the molten iron before being charged into the converter.
• a hydrogen gas, a propane gas, or a mixture gas of 50 vol% hydrogen and 50 vol% propane was supplied through a porous plug installed at the bottom of the converter.
• a test was conducted under, as comparative conditions, conditions where an argon gas was supplied as a bottom-blown gas during decarburization refining in a converter. Further, a test was conducted under conditions where only an argon gas was supplied by being bottom-blown during decarburization refining in a converter, and after the molten steel was discharged into a ladle, a hydrogen gas or a hydrocarbon gas was supplied as a circulating gas during a vacuum degassing treatment.
• Molten iron obtained by melting scrap in an electric furnace and blast-furnace molten pig iron were mixed in a converter-charging pot so as to adjust the amount of the mixed molten iron to 300 t.
• the carbon concentration [C] e of the molten iron at the time of discharging from the electric furnace was 0.2 to 0.3 mass%.
• the carbon concentration [C]i after the mixing was 2.5 to 3.5 mass%.
• the molten iron thus mixed was charged into a converter and subjected to decarburization refining.
• an oxygen gas for decarburization was being supplied, an argon gas was supplied at 40 Nm 3 /min through a porous plug installed at the bottom of the converter. After the molten steel was discharged from the converter, the components were analyzed, and further a vacuum degassing treatment was performed. As the circulating gas in this case, an argon gas was used. Upon completion of the degassing treatment, casting was performed using a continuous casting machine.
• Molten iron obtained by melting scrap in an electric furnace and blast-furnace molten pig iron were mixed in a converter-charging pot so as to adjust the amount of the mixed molten iron to 300 t.
• the carbon concentration [C] e of the molten iron at the time of discharging from the electric furnace was 0.2 to 0.3 mass%.
• the carbon concentration [C]i after the mixing was 2.5 to 2.8 mass%.
• the molten iron thus mixed was charged into a converter and subjected to decarburization refining.
• an oxygen gas for decarburization was being supplied, an argon gas was supplied at 40 Nm 3 /min through a porous plug installed at the bottom of the converter. After the molten steel was discharged from the converter, the components were analyzed, and further a vacuum degassing treatment was performed.
• a hydrogen gas or a propane gas was used as the circulating gas in this case.
• casting was performed using a continuous casting machine.
• Molten iron obtained by melting scrap in an electric furnace and blast-furnace molten pig iron were mixed in a converter-charging pot so as to adjust the amount of the mixed molten iron to 300 t.
• the carbon concentration [C] e of the molten iron at the time of discharging from the electric furnace was 0.2 to 0.3 mass%.
• the carbon concentration [C]i after the mixing was 2.5 to 2.8 mass%.
• the molten iron thus mixed was charged into a converter and subjected to decarburization refining.
• an oxygen gas for decarburization was being supplied, an argon gas was supplied at 40 Nm 3 /min through a porous plug installed at the bottom of the converter.
• the components were analyzed, and further a vacuum degassing treatment was performed.
• a hydrogen gas or a propane gas was used as the circulating gas in this case.
• the components were analyzed during the vacuum degassing treatment, and the vacuum treatment was continued until the hydrogen concentration became equal to or lower than a predetermined concentration.
• casting was performed using a continuous casting machine.
• Molten iron obtained by melting scrap in an electric furnace and blast-furnace molten pig iron were mixed in a converter-charging pot so as to adjust the amount of the mixed molten iron to 300 t.
• the carbon concentration [C] e of the molten iron at the time of discharging from the electric furnace was 0.2 to 0.3 mass%.
• the carbon concentration [C]i after the mixing was 0.6 to 2.8 mass%.
• the molten iron thus mixed was charged into a converter and subjected to decarburization refining.
• both the nitrogen concentration [N] ⁇ of the molten steel at the time of discharging from the converter and the crude steel nitrogen concentration N were low.
• the hydrogen concentration [H] f of the molten steel at the time of discharging from the converter was high, the crude steel hydrogen concentration H was low as a result of performing the vacuum degassing treatment.
• the vacuum degassing treatment time was found not to be prolonged.
• Molten iron obtained by melting reduced iron in an electric furnace and blast-furnace molten pig iron were mixed in a converter-charging pot so as to adjust the amount of the mixed molten iron to 300 t.
• the carbon concentration [C] e of the molten iron at the time of discharging from the electric furnace was 1.0 to 1.1 mass%.
• the carbon concentrations [C]i in tests No. 31, 36, and 41 in which unmixed molten iron was used were 0.9 mass%, while the carbon concentrations [C]i of other mixed molten irons were 1.4 to 2.9 mass%.
• unmixed molten iron or mixed molten iron was charged into a converter and subjected to decarburization refining. While an oxygen gas for decarburization was being supplied, a hydrogen gas or a propane gas or a mixture gas of these gases was supplied at 40 Nm 3 /min through a porous plug installed at the bottom of the converter. After the molten steel was discharged from the converter, the components were analyzed, and further a vacuum degassing treatment was performed. As the circulating gas in this case, an argon gas was used. Upon completion of the degassing treatment, casting was performed using a continuous casting machine.
• both the nitrogen concentration [N] ⁇ of the molten steel at the time of discharging from the converter and the crude steel nitrogen concentration N were low.
• the hydrogen concentration [H] f of the molten steel at the time of discharging from the converter was high, the crude steel hydrogen concentration H was low as a result of performing the vacuum degassing treatment.
• the vacuum degassing treatment time was found not to be prolonged.
• the method for refining molten iron according to the present invention can stably produce low-nitrogen steel with a nitrogen concentration of 30 mass ppm or lower under the condition of an increased amount of cold iron source used, without a significant decrease in productivity or cost increase, and without adding to the amount of slag generated or the amount of CO 2 generated.
• This method is industrially useful in that it allows existing integrated ironworks to reduce CO 2 emissions and produce high-grade steels at the same time while using blast-furnace molten pig iron and a cold iron source in combination.

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• Chemical & Material Sciences (AREA)
• Engineering & Computer Science (AREA)
• Materials Engineering (AREA)
• Metallurgy (AREA)
• Organic Chemistry (AREA)
• Manufacturing & Machinery (AREA)
• Treatment Of Steel In Its Molten State (AREA)
• Refinement Of Pig-Iron, Manufacture Of Cast Iron, And Steel Manufacture Other Than In Revolving Furnaces (AREA)

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• 2022
  • 2022-04-19 JP JP2022545913A patent/JP7384294B2/ja active Active
  • 2022-04-19 CN CN202280037168.2A patent/CN117377781A/zh active Pending
  • 2022-04-19 EP EP22811072.2A patent/EP4328330A1/fr active Pending
  • 2022-04-19 US US18/289,918 patent/US20240271233A1/en active Pending
  • 2022-04-19 KR KR1020237037654A patent/KR20230162108A/ko unknown
  • 2022-04-19 WO PCT/JP2022/018168 patent/WO2022249798A1/fr active Application Filing
  • 2022-04-19 BR BR112023024464A patent/BR112023024464A2/pt unknown
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