US3800630A - Procedure and installation for continuous steel making - Google Patents

Procedure and installation for continuous steel making Download PDF

Info

Publication number
US3800630A
US3800630A US3800630DA US3800630A US 3800630 A US3800630 A US 3800630A US 3800630D A US3800630D A US 3800630DA US 3800630 A US3800630 A US 3800630A
Authority
US
United States
Prior art keywords
slag
iron
steel
stream
metal
Prior art date
Legal status (The legal status 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 status listed.)
Expired - Lifetime
Application number
Other languages
English (en)
Inventor
I Tripsa
I Potoceanu
C Popescu
C Cazan
I Nisipeanu
C Velicov
N Furnicescu
E Berceanu
D Cosma
O Tanasescu
N Deica
I Martin
D Dulama
N Kraft
G Driscu
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
CONSILUIL NAT PENTRU STIINTA S
CONSILUIL NAT PENTRU STIINTA SI TECHNOLOGIE RU
Original Assignee
CONSILUIL NAT PENTRU STIINTA S
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 CONSILUIL NAT PENTRU STIINTA S filed Critical CONSILUIL NAT PENTRU STIINTA S
Application granted granted Critical
Publication of US3800630A publication Critical patent/US3800630A/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Images

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
    • C21C5/00—Manufacture of carbon-steel, e.g. plain mild steel, medium carbon steel or cast steel or stainless steel
    • C21C5/56—Manufacture of steel by other methods
    • C21C5/567—Manufacture of steel by other methods operating in a continuous way
    • 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
    • Y02P10/143—Reduction of greenhouse gas [GHG] emissions of methane [CH4]
    • 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
    • Y02P10/20—Recycling

Definitions

  • ABSTRACT 'A process for the continuous production of steel wherein a stream of iron, admixed with alloying ing redients, slag-forming elements and the like is atomized with compressed air at a pressure of 7 to 8 atmospheres to remove phosphorous, silicon andmanganese.
  • the melt is continuously drawn from the collecting basin in this chamber beneath the slag layer and is then atomizedby directing a blast of oxygen at the stream of iron to decarburize the melt which is thereupon collected, separated from slag and finely vacuum-processed and alloyed, all in a continuous stream.
  • liquid cast iron is introduced vertically and continuously into the apparatus through a funnel and is atomized by means of oxygen under pressure which sweeps away powdery fusing agents as, for example, lime and fluorine, the latter being necessary in the refining process.
  • the drops of cast iron react quickly with the oxygen and the fusing agents and are turned into steel, which is collected at the lower part of the apparatus, is deoxidized and is cast by means of a continuous casting machine.
  • cast iron is continuously introduced into a container and is intensely blown upon with the oxygen and fusing agents introduced through a nozzle similar to those used in oxygen converters. Owing to the carbon oxide given off,'the metal bath mixes with the slagand is turned into emulsion, which overflows into a second container, where the steel thus made separates from slag, is deoxidized and is discharged into a continuous casting machine.
  • the disadvantage of the two procedures lies in the high loss in of iron swept away with the discharged gases, for oxidation occurs at high temperatures, the cast iron having a high carbon content while on the other hand such losses are due to the fact that iron drops are mechanically swept away by the slag, which is directly discharged from the atomizing aggregate without any previous decanting.
  • the combustion gases with a high carbon oxide content given off in the decarburization stage are burnt with preheated air above the decanting, alloying and final deoxidation baths, after which their heat content is recovered in conventional regenerators and final alloying and deoxidation are effected, the melt being protected by a layer of synthetic slag introduced in powdery form and discharged from the respective bath in counter-current with thesteel made, and recirculated, also in counter-current, during the decarburization stage, whence, together with the slag resulting during the latter stage, it is recirculated in the cast iron atomizing unit where, recirculating in counter-current with the metal melt, it assimilates the silicon oxides given off in the respective stage so that a basicity ranging from 1.8 to 2.2 is reached.
  • the installation for carrying out the method of the present invention is made up of a mixer into which molten cast iron flows continuously from the furnace in a strain.
  • the unit is shaped like the frustum of a cone and provided with a funnel with a calibrated orifice for feeding molten metal, with means for feeding fusing agents and compressed air and with a sole-plate continued at one end by a melt-discharging channel and at the other end, by a slag-discharging trough.
  • the installation also includes a cylindrical decarburization container provided with facilities for blowing oxygen and additional ferrous material.
  • the capacity of these facilities is at least fifteen times greater than the per minute output of metal melt.
  • a lateral orifice connects the blowing facilities with a decanting vessel, which may be directly connected with the final deoxidation and alloying vessel by means of a siphon trap or may be initially connected to the ascending pipe of a vacuum processing aggregate which has an oblong, possibly an oval, vacuum chamber and is connected by means of a descending pipe to the final alloying and deoxidation vessel.
  • the latter vessel is provided with orifices for the introduction and discharge of synthetic slag in counter-current; the slag is-recirculated in the decanting vessel and is further recirculated, together with the slag resulting from decarburization in the cast iron atomizing aggregate through suitable orifices.
  • the cast iron discharged from one or several furnaces flows in the form of a molten-iron stream 1 along a trough 2 where a layer of furnace slag 3 is separated by means of a conventional device 4 in a mixer 5.
  • the mixer 5 is provided with devices for the introduction of powdery reagents, preferably by means of a gas (nitrogen or methane); and for the separation 'of desulphurization slag, which is subsequently discharged.
  • the slag in the mixer 5 or along the trough 2 is treated with common active desulphurization agents, for example lime, sodium carbonate, calcium carbide, aluminum., which are introduced with the assistance of a proportioning device 6, sulphur activity during this stage being at its highest owing to the high carbon, silicon and phosphorus content.
  • desulphurization agents for example lime, sodium carbonate, calcium carbide, aluminum.
  • the liquid cast iron is separated from a first slag layer 7 by means of a conventional device (eg stripper 8), and flows continuously into a funnel 9 with a calibrated orifice through which the molten-metal stream is passed with a view to atomization.
  • the calibrated orifice of the funnel 9 may have any section desiredincluding a circular one, though to minimize thelpressure of the air necessary for suitable cast iron atomizing, a rectangular or elongated section is tobe preferred, so that atomization of the cast iron jet in the form of small drops should be achieved with air at a pressure of 2-8 atm.
  • Compressed air is intro symbolized through two pipes (10a and 10b), which are parallel to' the flat cast iron jet; the pipes are water-cooled and slope radially at an acute angle of 10 to 80 as against the vertical.
  • the inside diameter of the horizontal pipes (10a and 10b is 10-50 times greater than the width of the slits through which compressed air is blown in.
  • the atomized cast iron flows in the form of fine drops 12 into an atomizing unit 13.
  • the second stage of the metal melt processing takes place, during which the silicon, manganese and phosphorus are eliminated, the cast iron being atomized with the help of air and fusing agents and moderate temperatures (1,300l,400C) being thus obtained. At these temperatures these elements are practically completely eliminated while the carbon in the cast iron is partially oxidized, the carbon content being maintained over 2.5 3 percent. The lower temperatures result in smaller losses of iron swept away with the discharged gases as well as in enhanced durability of the lining of the cast iron atomizing unit.
  • the atomizing unit 13 has a metal body in the shape of the frustum of a pyramid lined with refractory materials able to withstand the temperatures developed as a result of the intensive reactions in the oxidation of the silicon, manganese and phosphorus in the cast iron, and of part of the carbon in the cast iron, as well as full combustion of the carbon oxides produced.
  • the unit is provided with a basin 15, in which the metal melt and the slag collect; at one end the sole-plate continues as the channel 19 for continuous discharge of the melt after continuous separation of another slag layer 14. It is through channel 19 that the metal melt is introduced into the decarburization container 20.
  • the sole-plate 14 of the atomizing unit 13 terminates in an elongated trough 16 where the metal drops in the slag are decanted and the iron oxides in the slag are reduced.
  • the discharged slag 14 is introduced into a water-jet granulation device which is not shown.
  • the decarburization chamber 20, which is preferably cylindrical is in a vertical position and has a capacity at least fifteen times greater than the per minute output of the metal bath.
  • the channel 19 along which the metal melt flows into the chamber 20 may have any section and can be located at various levels, though it is preferable that the melt should be introduced tangentially at the bottom of the chamber 20 to ensure good mixing of the metal bath in the container and consequently rapid dilution of the carbon content in the fresh portions of the metal bath.
  • the decarburization chamber 20 is provided with one or more conventional nozzles 22 designed for blowing pure technical oxygen, as well as with orifices 23 and conventional devices (which are not shown in the drawing) feeding powdery fusing agents (lime, fluorides, ore, cinder, etc.) and additional iron for cooling the bath, in the form of scrap iron, metallized pellets or iron sponge.
  • powdery fusing agents limestone, fluorides, ore, cinder, etc.
  • additional iron for cooling the bath, in the form of scrap iron, metallized pellets or iron sponge.
  • the decarburization-chamber 20 sustains the third stage in the processing of the metal melt; the latter reacts intensely with oxygen and fusing agents, a steel and slag emulsion being thus obtained, which is discharged through a lateral opening 25 of the chamber 20 into a decanting vessel 23.
  • the metal bath in the decarburization chamber 20 In order to reduce the loss of iron, which is swept away with the discharged gases, the metal bath in the decarburization chamber 20 always contains,'as has been shown above, a volume at least 15 times greater than the per minute output of metal melt so that the carbon content is diluted after introduction of every portion of the melt into the chamber 20.
  • the carbon content in the decarburization container 16 being kept constant, at a value ranging from 0.2 to 0.8 percent C depending on the quality of the steel to. be made, losses of iron with the burnt gases are diminished to a minimum.
  • the metal bath is overheated and, in order to keep the temperature at a constant level l,520 1,670C, depending on the brand of the steel to be made cooling materials must be introduced.
  • the necessary quantities of iron oxide (cinder) and metal iron in the form of pieces of calibrated dimensions, scrap iron, metallized pellets and iron sponge, are continuously introduced into the chamber through the orifice 23. This results inoptimum use of the reaction heat, a rise in steel making efficiency and dilution of the carbon content of the metal melt in the decarburization chamber 20.
  • the decarburization chamber 20 has a discharge orifice (which is not shown in the drawing.) which is generally closed but maybe opened in order to discharge the melt upon a prolonged interruption in the running of the installation.
  • the decarburization vessel 29 has a vault 24 which it shares with the decarburization chamber 20; the latter is provided with an orifice 26 through which the preheated air required for the burning of gases yielded I in the decarburization stage is blown.
  • the gases contain carbon oxide.
  • the recuperator in which the air is pre-heated is not shown in the FIGURE.
  • the burnt gases are directed towards the stage of final decarburization and alloying of steel by means of a channel 42 located at the upper part of the' decanting vessel 29.
  • the decanting vessel 23 is also provided with a channel' 26b, which serves to discharge the slag layer 70 resulting from decarburization and has an orifice 28,
  • the vacuum chamber has an elongated, oval, section about seven times greater than its width so that the time during which the vacuum acts on the same portion of steel is 3-4 timeslonger than the time it takes the steel to pass through the vacuum installation commonly used, or is equivalent to the sum total of the time during which the vacuum acts on the steel, if there is repeated passage after recirculation through installations of this type.
  • argon penetrates into pipe 31 for admission of the metal melt, as the latter consists of rimming steel able to generate a sufficient amount which is generally blockedfand whichserves to discharge steel when the installation is brought to standstill.
  • THe vessel has a siphon trap 29, through which rimming steel is discharged towards the casting installation, and an orifice 30 to which a pipe' 31a is connected, the latter coming from an aggregate 32 processing the metal melt under vacuum when killed steel is to be obtained. 7 q
  • the vacuum processing aggregate 32 has a vacuum chamber of anelongated, possibly oval, shape, two pipes 31a and 31b for feeding and discharging steel, a pipe 31c connected to the vacuum pump for gas discharge, and locks 33 for addition of ferro-alloys and fusing agent's under vacuum conditions, if necessary.
  • Two or more vacuum processing aggregates 32 may be mounted in parallel so that, in case one unit is disabled, another-aggregate may be used and the continuous steel-making installation is not be kept at a standstill for a long time.
  • the fourth technological stage takes place in the chamber of the vacuum processing aggregate32; it-consists of deoxidation by the carbon in the metal melt, and in the removal of gas from the melt. A low content of gases and non-metal inclusions is thus ensured in the steel made.
  • the vessel 35 in the vessel serves to introduce the necessary ferroalloys (ferro-manganese, ferro-silicon, etc.) in granulated or melted condition and in the quantities needed to obtain the chemical composition prescribed for the various brands of steel to be made, including alloy steel.
  • ferroalloys ferro-manganese, ferro-silicon, etc.
  • the steel is discharged, preferably into continuous casting machines, thoughcommon ladles may also be used.
  • the steel is introduced into ingot or casting molds so that ingots or castings are obtained.
  • a second casting machine or several such casting machines may be used without the continuous making of steel being interrupted.
  • the vessel for final deoxidization and alloying of killed steel 34 is shaped like an elongated trough and is provided, as has already been shown, with an orifice 35a feeding powdery or liquid ferro-alloys, with another orifice 35b feeding a powdery mixture that forms deoxidizing slag, with a siphon trap for steel discharge without anyslag being swept along towards the continuous or common casting machines 40, with yet another orifice 41, which is permanently stopped and serves to discharge the contents when the installation is brought to a standstill for along time, and with a channel 43 through which the burnt gases are discharged towards the chimney stack.
  • the burnt gases are directed from the decarburization stage through channel 42.
  • the-slag 14 goes along a trough 16 where the metal drops swept away mechanically are decanted, and is subsequently discharged. It is in the same trough that the iron oxides in the slag can be reduced by means of the carbon in the metal bath or, if
  • the slag discharged possesses a comparatively reduced basicity (1.8-2.2) owing to assimilation of the silicon oxides produced in the atomizing installation andcan consequently be used as building material, the
  • the installation may be provided with various orifices for visual monitoring, gauges to check the running of all aggregates, facilities for centralization of the controls of the installation at one or morecontrol points as well as with facilities enabling the use of electronic computers with a static or dynamic operation regime to control the steel-making process in the respective installation.
  • the silicon content decreases to the final value of 0.48 to 1.03 wt percent; the manganese content decreases from its initial value of 0.83 to 1.22 wt percent to values below 0.05 wt percent; the phosphorus content decreases from its initial value of 0.051 to 0.107 wt percent to 0.008 to 0.036 wt percent; the sulphur content further decreases from 0.013 to 0.042 wt percent tothe final value of 0.002 to 0.021 wt percent, and the carbon content decreases from its initial value of 3.79 to 4.21 wt percent to 2.84 to 3.09 wt percent. Consequently on issuing from the atomizing aggregate 13 the metal melt practically consists only of iron and carbon.
  • the carbon content decreases to 0.2 wt percent for example, and this value is kept constant in the container.
  • the carbon content of the metal melt further decreases owing to intense reaction with emulsion slag, so that the carbon content in the decanting bath is kept constant: 0.10 wt percent, in the example given above.
  • the final composition of steel is obtained by adding the required quantities of ferro-alloys to the final deoxidization and alloying bath 36, to achieve a pre-established rise in the content of carbon, silicon, manganese and other alloying elements.
  • the present invention offers the following advantages: I
  • the heat is used to heat the metal melt and maintain it at the required temperature of 1,5201,670C until the steel is discharged from the installation; to smelt iron waste, metallized pellets and iron sponge, and to reduce the iron oxides in the cinder and other materials introduced into the decarburization container. To this end complete combustion of the gases resulting from the decarburization process is ensured in the steel-making installation, and part of the physical heat of the discharged gases is recovered and is used to preheat the combustion air.
  • Oxygen consumption per ton of steel is reduced to a minimum for the processes of silicon, manganese and phosphorus oxidation and about 25 percent of the oxidation of the carbon in the cast iron are achieved by means of the oxygen used in the atomizing of cast iron. Furthermore for the oxidation of the carbon in the decarburization container use is made of part of the oxygen brought by the iron oxides in the cinder and in the other materials that are added.
  • a method of making a steel comprising the steps of:
  • step (b) continuously atomizing the molten iron stream treated in step (a) and depositing, the atomized droplets of molten iron'through a slag layer into a first molten-metal bath;

Landscapes

  • Engineering & Computer Science (AREA)
  • Chemical & Material Sciences (AREA)
  • Manufacturing & Machinery (AREA)
  • Materials Engineering (AREA)
  • Metallurgy (AREA)
  • Organic Chemistry (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)
US3800630D 1970-10-08 1971-10-01 Procedure and installation for continuous steel making Expired - Lifetime US3800630A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
RO6463270A RO55785A2 (de) 1970-10-08 1970-10-08

Publications (1)

Publication Number Publication Date
US3800630A true US3800630A (en) 1974-04-02

Family

ID=20088210

Family Applications (1)

Application Number Title Priority Date Filing Date
US3800630D Expired - Lifetime US3800630A (en) 1970-10-08 1971-10-01 Procedure and installation for continuous steel making

Country Status (9)

Country Link
US (1) US3800630A (de)
AT (1) AT318676B (de)
AU (1) AU464758B2 (de)
BE (1) BE773038A (de)
BR (1) BR7106734D0 (de)
DE (1) DE2144962C3 (de)
FR (1) FR2112273B1 (de)
GB (1) GB1350499A (de)
RO (1) RO55785A2 (de)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0233404A1 (de) * 1986-01-15 1987-08-26 Italimpianti Of America Incorporated Verfahren und Anlage zur kontinuierlichen Herstellung von Stahl aus Erz
US4890821A (en) * 1980-04-08 1990-01-02 Nixon Ivor G Metallurgical processes

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
LU86689A1 (fr) * 1985-12-03 1987-05-04 Centro Speriment Metallurg Procede d'epuration continue de fonte en fusion

Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2665982A (en) * 1949-05-05 1954-01-12 Air Reduction Desulfurization and decarburization of iron and iron alloys
US2969282A (en) * 1959-05-06 1961-01-24 British Oxygen Co Ltd Treatment of ferrous metal
US3519059A (en) * 1967-07-12 1970-07-07 Viktor Grigorievich Voskoboini Method of vacuum slag refining of metal in the course of continuous casting
US3663205A (en) * 1966-09-23 1972-05-16 British Iron Steel Research Method of refining ferrous metals
US3672870A (en) * 1966-05-23 1972-06-27 British Iron Steel Research Spray refining

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2665982A (en) * 1949-05-05 1954-01-12 Air Reduction Desulfurization and decarburization of iron and iron alloys
US2969282A (en) * 1959-05-06 1961-01-24 British Oxygen Co Ltd Treatment of ferrous metal
US3672870A (en) * 1966-05-23 1972-06-27 British Iron Steel Research Spray refining
US3663205A (en) * 1966-09-23 1972-05-16 British Iron Steel Research Method of refining ferrous metals
US3519059A (en) * 1967-07-12 1970-07-07 Viktor Grigorievich Voskoboini Method of vacuum slag refining of metal in the course of continuous casting

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4890821A (en) * 1980-04-08 1990-01-02 Nixon Ivor G Metallurgical processes
EP0233404A1 (de) * 1986-01-15 1987-08-26 Italimpianti Of America Incorporated Verfahren und Anlage zur kontinuierlichen Herstellung von Stahl aus Erz

Also Published As

Publication number Publication date
BR7106734D0 (pt) 1973-04-05
FR2112273B1 (de) 1975-02-07
AT318676B (de) 1974-11-11
AU3407071A (en) 1973-04-05
FR2112273A1 (de) 1972-06-16
BE773038A (fr) 1972-01-17
DE2144962C3 (de) 1974-06-12
AU464758B2 (en) 1975-09-04
DE2144962B2 (de) 1973-11-15
DE2144962A1 (de) 1972-04-13
GB1350499A (en) 1974-04-18
RO55785A2 (de) 1974-01-03

Similar Documents

Publication Publication Date Title
US4457777A (en) Steelmaking
JP4195106B2 (ja) 合金鋼の製造方法および合金鋼の製造プラント
US3565605A (en) Process for the continuous refining of metals
US4612043A (en) Steel making method
US4726839A (en) Process and an arrangement for the production of steel from sponge iron
US3356490A (en) Refining pig iron
US4052197A (en) Process for making steel from pig iron
EP0328677B1 (de) Ofen und verfahren zur reduktion eines chromvorproduktes durch schmelzen
US4808219A (en) Method for treating metal melts and apparatus for carrying out the method
US3800630A (en) Procedure and installation for continuous steel making
US4944799A (en) Method of producing stainless molten steel by smelting reduction
US3672869A (en) Continuous metallurgical process
US4094495A (en) Method and apparatus for the production of quality steels
RU2566230C2 (ru) Способ переработки в кислородном конвертере низкокремнистого ванадийсодержащего металлического расплава
JP3719056B2 (ja) 清浄性に優れた極低炭素鋼の製造方法
KR900002710B1 (ko) 급속탈탄 제강공정
JP4686880B2 (ja) 溶銑の脱燐方法
JP3333339B2 (ja) 脱炭滓をリサイクルする転炉製鋼法
US4199350A (en) Method for the production of quality steels
US3251679A (en) Method of refining an iron melt
US3782921A (en) Production of steel with a controlled phosphorus content
JP3668172B2 (ja) 溶銑の精錬方法
US4676825A (en) Hot metal desulphurizing and dephosphorizing process
SU594181A1 (ru) Способ производства нержавеющей стали
KR100377273B1 (ko) 레이들 슬래그 조제방법