EP0163784A1 - Two stage deoxidation process in steel-making - Google Patents

Two stage deoxidation process in steel-making Download PDF

Info

Publication number
EP0163784A1
EP0163784A1 EP84303555A EP84303555A EP0163784A1 EP 0163784 A1 EP0163784 A1 EP 0163784A1 EP 84303555 A EP84303555 A EP 84303555A EP 84303555 A EP84303555 A EP 84303555A EP 0163784 A1 EP0163784 A1 EP 0163784A1
Authority
EP
European Patent Office
Prior art keywords
steel
molten steel
ladle
silicon
partially
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.)
Granted
Application number
EP84303555A
Other languages
German (de)
French (fr)
Other versions
EP0163784B1 (en
Inventor
Maw-Cheng Shieh
Seng-Jung Chen
Li-Jung Hu
Jin-Luh Su
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.)
China Steel Corp
Original Assignee
China Steel Corp
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 China Steel Corp filed Critical China Steel Corp
Priority to DE8484303555T priority Critical patent/DE3480350D1/en
Priority to AT84303555T priority patent/ATE47727T1/en
Priority to EP84303555A priority patent/EP0163784B1/en
Priority to ZA852015A priority patent/ZA852015B/en
Priority to AU40220/85A priority patent/AU567212B2/en
Publication of EP0163784A1 publication Critical patent/EP0163784A1/en
Application granted granted Critical
Publication of EP0163784B1 publication Critical patent/EP0163784B1/en
Expired legal-status Critical Current

Links

Images

Classifications

    • CCHEMISTRY; METALLURGY
    • C21METALLURGY OF IRON
    • C21CPROCESSING OF PIG-IRON, e.g. REFINING, MANUFACTURE OF WROUGHT-IRON OR STEEL; TREATMENT IN MOLTEN STATE OF FERROUS ALLOYS
    • C21C7/00Treating molten ferrous alloys, e.g. steel, not covered by groups C21C1/00 - C21C5/00
    • C21C7/0056Treating molten ferrous alloys, e.g. steel, not covered by groups C21C1/00 - C21C5/00 using cored wires
    • CCHEMISTRY; METALLURGY
    • C21METALLURGY OF IRON
    • C21CPROCESSING OF PIG-IRON, e.g. REFINING, MANUFACTURE OF WROUGHT-IRON OR STEEL; TREATMENT IN MOLTEN STATE OF FERROUS ALLOYS
    • C21C7/00Treating molten ferrous alloys, e.g. steel, not covered by groups C21C1/00 - C21C5/00
    • C21C7/04Removing impurities by adding a treating agent
    • C21C7/06Deoxidising, e.g. killing

Definitions

  • This invention concerns with Weak Pre-deoxictation practice in steelmaking. Adding Si contained ferroalloy during tapping stage as weak pre-deoxidation practice, this new practice could achieve lower production cost and high quality steel products. For rimmed steel production very mino addition of deoxidizer results in higher freo oxygen contain in molten rimmed steel, which would react with solute element in molten steel, a solid skin layer around the ingot surface is formed. i
  • the deoxidizer (Al, Si, Ti, Mn) added during tapping process is oxidized by the free oxygen in molten steel.
  • the reaction is shown below:
  • the fully killed molten steel could be casted continuous casting process.
  • the production yield and internal quality of the continuous caated products is superior than that of ingot.
  • Lower recovery rate and higher addition amount of deoxidizer for fully killed steel causes higher production costs and results in the residual of deoxidizing formations remained in steel.
  • Such residual deoxidation formations is harmful to processing formability while the Weak Pre-deoxidation process could vanish the defects stated above and provides lower cost higher clenniness and higher quality steel products.
  • alumina cluster (A1 2 0 3 ) forms in molten steel and remains in solid steel as inclusion, which could not be elongated during deformation, thus interfere the cold heading or working formability.
  • the objective of this new process stated above is to overcome the shortness of deoxidation practice, that is to reduce work hardening effect.
  • any Si contained ferroalloy could not be added during steelmaking.
  • Such deoxidation concept is modified by this new deoxidation process, during tapping (of top blowing furnace, bottom blowing furnace, top and bottom combined blowing furnace or electric arc furnace) appropriate amount of S i contained ferroalloy could be added in the condition of no Si remained in molten steel.
  • Free oxygen content of the molten steel in ladle could be reduced as Si contained ferroalloy added then the ladle is transferred to Al-wire feeder system or ladle injection treating station to proceed the final stage deoxidatio: with Al and/or Ti killing, or other composition adjustment.
  • This new process will increase the recovery rate of deoxidizer, decrease the amount of deoxidizer and ferroalloy consumption and save production cost. Because of less deoxidizer and alloy addition, deoxidized formations could be reduced that would remarkably improve the internal cleaniness of the steel products.
  • the major premise of this invention is to add Si contained ferro- alloy as weak pre-deoxidation process with the furance (such as top blowing type, botton blowing type, top and bottom combined type or electric arc furnace) or during tapping,.then following by final stage deoxidation process by Al and/or Ti addition Al-wire feeder system and/or ladle injection treating station are the undeficient equipments for this new deoxidation process.
  • Fig. 3(a) & 3(b) compare the Si content in the liquid steel between WPD Process and non-WFI) Process.
  • Fig. 3(a) shows the distribution of Si contents in the final molten steel treated by weak pre-deoxldizing with Si contained ferroalloy.
  • Fig. 3(b) shows the distribution of Si contents in the final molten steel without WPD treatment.
  • Fig. 3(a) & 3(b) indicates the percent of the number of heats which contain Si less than 0.02% in the liquid steel by using WPD Process is 96.8%, while that of non-WPD Process is 95.8%.
  • the data obviously shows that the proportion of Si content below 0.02% in the liquid steel of WPD Process is even a little bit higher than that of non-WPD Process.
  • the S i content analyzed by spectroscope is total Si content (including silica), thus confirms that S i contained ferroalloy will not cause Si to be retained in the liquid steel.
  • Si will react with free oxygen first and forms silicon dioxide (Si0 2 ) particles, which distribute in the whole liquid steel. Manganese will then reacts with the oxygen around SiO 2 and forms Silicon-manganese oxides, which can float up almost completely after gas stirring. Therefore, it is the characteristics of the present invention that by adding appropriate amount of Si contained ferroalloy during tapping (or into furnace) the free osygen content can be reduced effectively before Al and/or Ti addition, without fearing of Si being retained.
  • Fig. 4 shows the comparison of the rate of Al recovery between Al-killed steel produced by Weak Pre-Deoxidation Process and conventional deoxidation process.
  • the rate of Al recovery was evidently increased by this invention as indicated in Fig. 4, that is due to the content of free oxygen in molten steel is remarkably decreased. Because of higher recovery rate of Al, caused less Al addition, deoxidation formations could be effectively reduced. Consequently, the internal cleaniness and surface quality of the steel product was remarkably improved by this new process.
  • Table 1 shows the comparison of free oxygen content between WPD Process and conventional deoxidation process before aluminum and/or titanium addition.
  • Purpose of this invention is to lower down the free oxygen content of molten steel as possible before the addition of deoxidizers (aluminum and/or titanium). (The key point of this process is to make sure that there is no silicon remained in the molten steel)
  • deoxidizers aluminum and/or titanium.
  • the amount of free oxygen content lowered can be controlled directly by adjusting the amount of Si contained ferroalloy addition. Owing to the decrease of free oxygen content, recovery of aluminum can be improved, cost can bo lowered, and the quality of steel products can be improved remarkably.
  • Table 2 shows the comparison of typical chemical compositions between the general cold working Al-killed steel grade and the steel designed according to this invention for the same end use.
  • the main difference is that typical chemical composition designed according to this invention has lower aluminum content than that of conventional Al-killed steel grade.
  • the reason for this composition design is to decrease the inclusion formation of deoxidation to get cleaner molten steel. Because of more deoxidizers are added, more chances to form inclusions would result and the cost is also higher. Therefore, the principle of chemical composition design by this invention is to lower the addition of deoxidizers such as aluminum and/or titanium under the condition of no poor deoxidation and good formability. And with the aid of WPD Process, the amount of deoxidizers added can be decreased, cleaner steel and lower production cost will be resulted.
  • This deoxidation method is also suitable for any other kind of Al-killed steel grade.
  • Table 3 shows the comparison of estimated index of inclusions between different deoxidation processes.
  • the main prupose of WPD Process is to improve the internal cleaniness, and improve the quality of casted steel.
  • the table obviously shows that under this new process, the estimated index of inclusions is much better than that of conventional process. It can also be sured that the WPI) Process has much improvement on internal quality of casted steel.
  • Table 4 shows the comparison of grinding speed of billets between different deoxidation processes. In respect of quality, the WPD Process improves not only the internal cleaniness of the casted steel, but also its surface quality. Data listed in the table represent pieces of billets to be ground within unit time (per hour).
  • the WPD Process can make much improvement on surfacial quality of casted steel, and save much surface conditioning cost.

Landscapes

  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Metallurgy (AREA)
  • Organic Chemistry (AREA)
  • Treatment Of Steel In Its Molten State (AREA)

Abstract

weak pre-deoxidation process (W.P.D. process) for the production of aluminium- and titanium-killed steel.
In this process an adequate amount of a silicium- containing ferro-alloy is added to the molten steel during its tapping.
The ladle is subsequently transferred to an aluminium wire feeder or to a ladle-injection treating equipment for performing the final stage deoxidation process.

Description

  • This invention concerns with Weak Pre-deoxictation practice in steelmaking. Adding Si contained ferroalloy during tapping stage as weak pre-deoxidation practice, this new practice could achieve lower production cost and high quality steel products. For rimmed steel production very mino addition of deoxidizer results in higher freo oxygen contain in molten rimmed steel, which would react with solute element in molten steel, a solid skin layer around the ingot surface is formed. i
  • Such solid skin layer possessing good surface quality and soft characteristics will improve cold heading formability of the steel products whereas the inner part of rimmed steel could not provided for higher grade application because of its poor cleaniness. High free oxygen in rimmed steel liquid, couldn't be casted by continuous casting process, casted ingot causes lower production yield. Rimmed steel couldn't be provided for special application for the reasons stated as above.
  • For fully killed steel, the deoxidizer (Al, Si, Ti, Mn) added during tapping process is oxidized by the free oxygen in molten steel. The reaction is shown below:
    • Figure imgb0001
      M: Deoxidizer, such as Al, Si, Ti, Mn etc.
    • (C): free oxygen in molten steel
    • x,y: coefficient
  • Because of lower free oxygen after deoxidizing, the fully killed molten steel could be casted continuous casting process. Generally speaking, the production yield and internal quality of the continuous caated products is superior than that of ingot. Lower recovery rate and higher addition amount of deoxidizer for fully killed steel causes higher production costs and results in the residual of deoxidizing formations remained in steel. Such residual deoxidation formations is harmful to processing formability while the Weak Pre-deoxidation process could vanish the defects stated above and provides lower cost higher clenniness and higher quality steel products.
  • producting steel for cold working or forming applications by continuous casting, fully killed steel is usually adopted to avoid casting incident and blow hole formation in steel, Al and/ or Ti is the major deoxidizer in continuous casting process. Killed steel for cold working or forming applications could be classified into Al-killed and Ti-killed steel according to the deoxidizer adopted. Al-killed steel as an example, in order to reduce work hardening effect, any Si contained ferroalloy could not be permitted to add into molten steel during steelmaking process, only Al is used as deoxidizer. Owing to the deoxidation reaction of Al (2A1 + 3[0] = Al2O3). alumina cluster (A1203) forms in molten steel and remains in solid steel as inclusion, which could not be elongated during deformation, thus interfere the cold heading or working formability. The objective of this new process stated above is to overcome the shortness of deoxidation practice, that is to reduce work hardening effect. For conventional Al-killed steel, any Si contained ferroalloy could not be added during steelmaking. Such deoxidation concept is modified by this new deoxidation process, during tapping (of top blowing furnace, bottom blowing furnace, top and bottom combined blowing furnace or electric arc furnace) appropriate amount of Si contained ferroalloy could be added in the condition of no Si remained in molten steel. Free oxygen content of the molten steel in ladle could be reduced as Si contained ferroalloy added then the ladle is transferred to Al-wire feeder system or ladle injection treating station to proceed the final stage deoxidatio: with Al and/or Ti killing, or other composition adjustment.
  • This new process will increase the recovery rate of deoxidizer, decrease the amount of deoxidizer and ferroalloy consumption and save production cost. Because of less deoxidizer and alloy addition, deoxidized formations could be reduced that would remarkably improve the internal cleaniness of the steel products. The major premise of this invention is to add Si contained ferro- alloy as weak pre-deoxidation process with the furance (such as top blowing type, botton blowing type, top and bottom combined type or electric arc furnace) or during tapping,.then following by final stage deoxidation process by Al and/or Ti addition Al-wire feeder system and/or ladle injection treating station are the undeficient equipments for this new deoxidation process. After treating by Al and/or Ti with this new process, good shrouding system should be adopted during continuous casting or ingot teemming process to protect the molten steel from reoxi- dizing by the atmosphere. Consequently, cleaner steel could be acquired by this new process. The explanation of this new process proceeding with various installation is described as following flow chart (Fig.1):
    • This invention will be explained in detail with some figures and tables as following:
    • Fig. 2 shows the relationship between the amount of Si contained ferroalloy added and the free oxygen content before adding aluminium as a deoxidizer into the liquid steel (which has no residual Si).
  • In general, in order to prevent the liquid steel from containing residual Si, no Si contained ferroalloy could be permitted to add into molten steel to adjust the chemical composition in producing Al-killed steel, ferromanganese is usually added. But manganese itself is not a good deoxidizer. Therefore, if weak pre-deoxidation with Si contained ferroalloy is not performed before Al addition in producing Al-killed steel, the residual free oxygen content in the liquid steel will be very high and unstable. Fig. 2 indicates that with appropriate amount of Si contained ferroalloy addition the free oxygen content in the liquid steel before Al deoxidation can evidently be lowered. By using this process, the recovery of deoxidizer can be improved and the oxides retained in the liquid steel after deoxidation can be reduced as well, thus the quality of bloom, slab and ingot can be improved. Fig. 3(a) & 3(b) compare the Si content in the liquid steel between WPD Process and non-WFI) Process. Fig. 3(a) shows the distribution of Si contents in the final molten steel treated by weak pre-deoxldizing with Si contained ferroalloy. Fig. 3(b) shows the distribution of Si contents in the final molten steel without WPD treatment.
  • Fig. 3(a) & 3(b) indicates the percent of the number of heats which contain Si less than 0.02% in the liquid steel by using WPD Process is 96.8%, while that of non-WPD Process is 95.8%. The data obviously shows that the proportion of Si content below 0.02% in the liquid steel of WPD Process is even a little bit higher than that of non-WPD Process. The Si content analyzed by spectroscope is total Si content (including silica), thus confirms that Si contained ferroalloy will not cause Si to be retained in the liquid steel. (It can also be confirmed by microscope.) While Si contained ferroalloy is added into liquid steel, Si will react with free oxygen first and forms silicon dioxide (Si02) particles, which distribute in the whole liquid steel. Manganese will then reacts with the oxygen around SiO2 and forms Silicon-manganese oxides, which can float up almost completely after gas stirring. Therefore, it is the characteristics of the present invention that by adding appropriate amount of Si contained ferroalloy during tapping (or into furnace) the free osygen content can be reduced effectively before Al and/or Ti addition, without fearing of Si being retained.
  • Fig. 4 shows the comparison of the rate of Al recovery between Al-killed steel produced by Weak Pre-Deoxidation Process and conventional deoxidation process. For A1-wire feeder system, the rate of Al recovery was evidently increased by this invention as indicated in Fig. 4, that is due to the content of free oxygen in molten steel is remarkably decreased. Because of higher recovery rate of Al, caused less Al addition, deoxidation formations could be effectively reduced. Consequently, the internal cleaniness and surface quality of the steel product was remarkably improved by this new process.
  • Table 1 shows the comparison of free oxygen content between WPD Process and conventional deoxidation process before aluminum and/or titanium addition.
  • Purpose of this invention is to lower down the free oxygen content of molten steel as possible before the addition of deoxidizers (aluminum and/or titanium). (The key point of this process is to make sure that there is no silicon remained in the molten steel) The data listed in the table obviously show that after WPD Proceas treatment the free oxygen content can be greatly decreased before the addition of deoxidizers.
  • The amount of free oxygen content lowered can be controlled directly by adjusting the amount of Si contained ferroalloy addition. Owing to the decrease of free oxygen content, recovery of aluminum can be improved, cost can bo lowered, and the quality of steel products can be improved remarkably.
  • Table 2 shows the comparison of typical chemical compositions between the general cold working Al-killed steel grade and the steel designed according to this invention for the same end use. The main difference is that typical chemical composition designed according to this invention has lower aluminum content than that of conventional Al-killed steel grade. The reason for this composition design is to decrease the inclusion formation of deoxidation to get cleaner molten steel. Because of more deoxidizers are added, more chances to form inclusions would result and the cost is also higher. Therefore, the principle of chemical composition design by this invention is to lower the addition of deoxidizers such as aluminum and/or titanium under the condition of no poor deoxidation and good formability. And with the aid of WPD Process, the amount of deoxidizers added can be decreased, cleaner steel and lower production cost will be resulted.
  • This deoxidation method is also suitable for any other kind of Al-killed steel grade.
  • Table 3 shows the comparison of estimated index of inclusions between different deoxidation processes. In respect of quality, the main prupose of WPD Process is to improve the internal cleaniness, and improve the quality of casted steel. The table obviously shows that under this new process, the estimated index of inclusions is much better than that of conventional process. It can also be sured that the WPI) Process has much improvement on internal quality of casted steel.
  • Table 4 shows the comparison of grinding speed of billets between different deoxidation processes. In respect of quality, the WPD Process improves not only the internal cleaniness of the casted steel, but also its surface quality. Data listed in the table represent pieces of billets to be ground within unit time (per hour).
  • (The worse in surfacial quality, the bigger in area and depth should be grinding, so less pieces of billets could be treated within unit time in order to get same level of surfacinl quality.)
  • This table shows that the grinding speed of billets treated by the VPD Process is faster than that of conventional deoxidation process.
  • Therefore, the WPD Process can make much improvement on surfacial quality of casted steel, and save much surface conditioning cost.
  • [II) Claims of this patent application:
    • 1) This is an invention of deoxidation process for Al-killed and/or Ti-killed steel for Basic Oxygen or Electric Arc Furnace Steel making processes. It includes:
      • (1) After blowing end or during tapping of Basic Oxygen or Electric Arc Furnace Steel making, Si contained ferroalloy is added to the molten steel as weak pre-deoxidation agent. After adding optimal Si contained ferroalloy, the free oxygen content of molten steel can be lowered efficiently whereas silicon will not remain in molten steel. It is this method which not only increases the recovery of aluminum and/or titanium, saves much production cost, improves surfacial and internal quality of steel which is good for formability, but also keeps steelmaking operation in good stability.
      • (2) According to the statements of this patent application as mentioned in item 1, the feature of the weak pre-deoxidation process is its type of deoxidation which is executed after blowing end and before aluminum and/or titanium deoxidizers addition.
      • (3) According to the statements of this patent application as mentioned in item 1, the weak pre-deoxidation process is quite different from that of conventional process. (conventional process is that Si contained ferroalloy can't be added as deoxidizing agent in Al-killed and/or Ti-killed steel to prevent from silicon retaining in molten steel). So addition of Si contained ferroalloy is a feature of this process.

Claims (10)

1. A method for the deoxidation of molten steel produced in a furnace by a steelmaking process, which method comprises:
(a) subjecting the produced molten steel to a pre-deoxidizing treatment by adding to said molten steel a silicon-containing ferroalloy in an amount effective to partially deoxidize said molten steely then
(b) treating the partially deoxidized molten steel with one or more deoxidizers and obtaining de- oxidized steel without substantial retention of silicon.
2. A method according to claim 1, wherein the produced molten steel is subjected to the pre-deoxidizing treatment in the furnace after a blowing step or during a tapping step of the steelmaking process.
3. A method according to either of claims 1 and 2, wherein molten steel produced by a basic oxygen or electric arc furnace steelmaking process is subjected to the pre-deoxidizing treatment.
4. A method according to any one of claims 1 to 3, wherein the partially deoxidized molten steel is treated with a deoxidizer consisting of one or both of Al or Ti.
5, A method according to any one of claims 1 to 4 wherein after the pre-deoxidizing treatment, silicon oxides are separated from the partially deoxidized molten-steel.
6. A method according to claim 5, wherein the silicon oxides are separated by gas stirring or bubbling.
7. A method according to either of claims 5 or 6 wherein after separation of the silicon oxides, the partially deoxidized molten steel is contained in a ladle and is treated with one or both of Al or Ti added by use of ladle injection treatment equipment or an Al wire or shot feeder.
8. A mathod according to any one of claims I to 7, wherein the free oxygen content. in the partially deoxidized steel is controlled by aajusting the amount of silicon-containing ferroalloy added during the pre-deoxidizing treatment.
9. A mathod according to any one of claims 1 to 8, wherein the obtained de-oxidized steel is continuously cast into steel products.
10. A method for the deoxidation of molten steel produced by a basic oxygen or electric arc furnace steelmaking process, which method comprises:
(a) after tapping the produoed molten steel into a ladle, subjecting the produced molten steel in said ladle to a pre-deoxidizing treatment by adding to said molten steel a silicon-containing ferro- alloy in an astount effective to partially deoxidize said molten steely
(b) separating silicon oxides from the partially deoxidized molten steel by gas stirring or bubbling in the ladle;
(c) treating the partially deoxidized, substantially silicon-free molten steel in a ladle with a deoxidizer consisting of one or both of Al or Ti to obtain deoxidized molten steel.
EP84303555A 1984-05-25 1984-05-25 Two stage deoxidation process in steel-making Expired EP0163784B1 (en)

Priority Applications (5)

Application Number Priority Date Filing Date Title
DE8484303555T DE3480350D1 (en) 1984-05-25 1984-05-25 Two stage deoxidation process in steel-making
AT84303555T ATE47727T1 (en) 1984-05-25 1984-05-25 TWO-STAGE DEOXIDATION PROCESS IN STEEL MANUFACTURE.
EP84303555A EP0163784B1 (en) 1984-05-25 1984-05-25 Two stage deoxidation process in steel-making
ZA852015A ZA852015B (en) 1984-05-25 1985-03-18 Si contained ferro-alloy addition as a weak pre-deoxidation process in steelmaking
AU40220/85A AU567212B2 (en) 1984-05-25 1985-03-21 Pre-deoxidation process in steelmaking

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
EP84303555A EP0163784B1 (en) 1984-05-25 1984-05-25 Two stage deoxidation process in steel-making
AU40220/85A AU567212B2 (en) 1984-05-25 1985-03-21 Pre-deoxidation process in steelmaking

Publications (2)

Publication Number Publication Date
EP0163784A1 true EP0163784A1 (en) 1985-12-11
EP0163784B1 EP0163784B1 (en) 1989-11-02

Family

ID=36838654

Family Applications (1)

Application Number Title Priority Date Filing Date
EP84303555A Expired EP0163784B1 (en) 1984-05-25 1984-05-25 Two stage deoxidation process in steel-making

Country Status (5)

Country Link
EP (1) EP0163784B1 (en)
AT (1) ATE47727T1 (en)
AU (1) AU567212B2 (en)
DE (1) DE3480350D1 (en)
ZA (1) ZA852015B (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2809745A1 (en) * 2000-06-05 2001-12-07 Sanyo Special Steel Co Ltd High cleanness steel production includes adding a deoxidizing agent to a ladle before pouring steel melt into the ladle or adding deoxidizing agent to the melt during pouring of the melt into the ladle
GB2406580A (en) * 2000-06-05 2005-04-06 Sanyo Special Steel Co Ltd High-cleanliness steel and processes for producing the same
GB2410252A (en) * 2000-06-05 2005-07-27 Sanyo Special Steel Co Ltd High-cleanliness steel and process for producing the same

Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2705196A (en) * 1952-02-20 1955-03-29 Manufacturers Chemical Corp Process for de-oxidizing a molten metal
DE957665C (en) * 1957-01-17 Max-Planck-Institut iur Eisenforschung e V, Dussel dorf Method and device for treating iron and steel baths
DE969295C (en) * 1954-01-27 1958-05-22 Hoesch Westfalenhuette Ag Use of steel or mirror iron to pre-deoxidize steel
FR2387292A1 (en) * 1977-04-14 1978-11-10 Siderurgie Fse Inst Rech Two=step deoxidation of steel - by pptn. of oxide(s) followed by slag metal exchange
EP0002929B1 (en) * 1977-12-22 1981-11-11 Uss Engineers And Consultants, Inc. Use of plain low carbon steels for electrical applications

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE957665C (en) * 1957-01-17 Max-Planck-Institut iur Eisenforschung e V, Dussel dorf Method and device for treating iron and steel baths
US2705196A (en) * 1952-02-20 1955-03-29 Manufacturers Chemical Corp Process for de-oxidizing a molten metal
DE969295C (en) * 1954-01-27 1958-05-22 Hoesch Westfalenhuette Ag Use of steel or mirror iron to pre-deoxidize steel
FR2387292A1 (en) * 1977-04-14 1978-11-10 Siderurgie Fse Inst Rech Two=step deoxidation of steel - by pptn. of oxide(s) followed by slag metal exchange
EP0002929B1 (en) * 1977-12-22 1981-11-11 Uss Engineers And Consultants, Inc. Use of plain low carbon steels for electrical applications

Cited By (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2809745A1 (en) * 2000-06-05 2001-12-07 Sanyo Special Steel Co Ltd High cleanness steel production includes adding a deoxidizing agent to a ladle before pouring steel melt into the ladle or adding deoxidizing agent to the melt during pouring of the melt into the ladle
WO2001094648A2 (en) * 2000-06-05 2001-12-13 Sanyo Special Steel Co., Ltd. High-cleanliness steel and process for producing the same
FR2812660A1 (en) * 2000-06-05 2002-02-08 Sanyo Special Steel Co Ltd HIGH-CLEAN STEEL AND PROCESS FOR PRODUCING THE SAME
WO2001094648A3 (en) * 2000-06-05 2002-08-08 Sanyo Special Steel Co Ltd High-cleanliness steel and process for producing the same
GB2381537A (en) * 2000-06-05 2003-05-07 Sanyo Special Steel Co Ltd High-cleanliness steel and process for producing the same
GB2406580A (en) * 2000-06-05 2005-04-06 Sanyo Special Steel Co Ltd High-cleanliness steel and processes for producing the same
GB2410252A (en) * 2000-06-05 2005-07-27 Sanyo Special Steel Co Ltd High-cleanliness steel and process for producing the same
GB2410252B (en) * 2000-06-05 2005-09-07 Sanyo Special Steel Co Ltd High-cleanliness steel and process for producing the same
GB2406580B (en) * 2000-06-05 2005-09-07 Sanyo Special Steel Co Ltd High-cleanliness steel and process for producing the same
GB2381537B (en) * 2000-06-05 2005-09-14 Sanyo Special Steel Co Ltd High-cleanliness steel and process for producing the same
US7396378B2 (en) 2000-06-05 2008-07-08 Sanyo Special Steel Co., Ltd. Process for producing a high cleanliness steel
DE10196303B3 (en) * 2000-06-05 2014-11-13 Sanyo Special Steel Co., Ltd. Process for producing a high purity steel

Also Published As

Publication number Publication date
ATE47727T1 (en) 1989-11-15
AU567212B2 (en) 1987-11-12
ZA852015B (en) 1985-09-19
DE3480350D1 (en) 1989-12-07
EP0163784B1 (en) 1989-11-02
AU4022085A (en) 1986-09-25

Similar Documents

Publication Publication Date Title
CN114085953B (en) Control method for acid dissolution of aluminum in aluminum-containing cold heading steel
EP0829546A1 (en) Process for producing aluminum-killed steel free of cluster
CN114058970B (en) Production method of bearing steel
CN111041352A (en) External refining production method of wire rod for cutting diamond wire
CN114182156A (en) Production method of low-aluminum carbon structural molten steel
CN115404393A (en) Production method of rare earth Ce treated 16MnHIC steel blank for flange
EP0163784A1 (en) Two stage deoxidation process in steel-making
US4741772A (en) Si contained ferroalloy addition as a weak pre-deoxidation process in steelmaking
US4060406A (en) Arc steelmaking
CN108642239B (en) Method for alloying molten steel silicon and treating calcium by using metal-containing calcium-silicon-iron alloy
US4170467A (en) Method for producing high chromium steels having extremely low carbon and nitrogen contents
US4168158A (en) Method for producing alloy steels having a high chromium content and an extremely low carbon content
CA1249724A (en) Si contained ferroalloy addition as a weak pre-deoxidation process in steelmaking
JP3473388B2 (en) Refining method of molten stainless steel
US4014683A (en) Method of making Drawing Quality steel
JPH04218644A (en) Fe-ni alloy cold rolled sheet excellent in cleanliness and etching pierceability and its manufacture
CN113930584B (en) Method for improving production stability of high-silicon aluminum killed steel
KR101018167B1 (en) Method for Manufacturing Steel with Low Sulfur
KR970010981A (en) Manufacturing Method of Silicon Deoxidation 304 Stainless Steel with Excellent Surface Quality
JP3404115B2 (en) Refining method of austenitic stainless steel with excellent hot workability
KR950010171B1 (en) Making method of high purity steel
GB934645A (en) Improvements in or relating to a process of producing refined molten iron and producing alloy steel therefrom
RU2031755C1 (en) Method to apply vacuum treatment to a steel containing too small amount of carbon at continuous casting in a flow line
Turkdogan Ladle deoxidation, desulphurisation and inclusions in steel–Part 2: Observations in practice
SU781218A1 (en) Method of low-alloy steel production

Legal Events

Date Code Title Description
PUAI Public reference made under article 153(3) epc to a published international application that has entered the european phase

Free format text: ORIGINAL CODE: 0009012

AK Designated contracting states

Designated state(s): AT BE CH DE FR GB IT LI LU NL SE

17P Request for examination filed

Effective date: 19860609

17Q First examination report despatched

Effective date: 19870430

GRAA (expected) grant

Free format text: ORIGINAL CODE: 0009210

AK Designated contracting states

Kind code of ref document: B1

Designated state(s): AT BE CH DE FR GB IT LI LU NL SE

REF Corresponds to:

Ref document number: 47727

Country of ref document: AT

Date of ref document: 19891115

Kind code of ref document: T

ITF It: translation for a ep patent filed
REF Corresponds to:

Ref document number: 3480350

Country of ref document: DE

Date of ref document: 19891207

ET Fr: translation filed
ITTA It: last paid annual fee
PLBE No opposition filed within time limit

Free format text: ORIGINAL CODE: 0009261

STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: NO OPPOSITION FILED WITHIN TIME LIMIT

26N No opposition filed
PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: GB

Payment date: 19940506

Year of fee payment: 11

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: SE

Payment date: 19940510

Year of fee payment: 11

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: FR

Payment date: 19940517

Year of fee payment: 11

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: CH

Payment date: 19940526

Year of fee payment: 11

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: BE

Payment date: 19940527

Year of fee payment: 11

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: NL

Payment date: 19940531

Year of fee payment: 11

Ref country code: LU

Payment date: 19940531

Year of fee payment: 11

EPTA Lu: last paid annual fee
EAL Se: european patent in force in sweden

Ref document number: 84303555.1

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: DE

Payment date: 19950505

Year of fee payment: 12

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: LU

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 19950525

Ref country code: GB

Effective date: 19950525

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: SE

Effective date: 19950526

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: AT

Payment date: 19950529

Year of fee payment: 12

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: LI

Effective date: 19950531

Ref country code: CH

Effective date: 19950531

Ref country code: BE

Effective date: 19950531

BERE Be: lapsed

Owner name: CHINA STEEL CORP.

Effective date: 19950531

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: NL

Effective date: 19951201

GBPC Gb: european patent ceased through non-payment of renewal fee

Effective date: 19950525

REG Reference to a national code

Ref country code: CH

Ref legal event code: PL

NLV4 Nl: lapsed or anulled due to non-payment of the annual fee

Effective date: 19951201

EUG Se: european patent has lapsed

Ref document number: 84303555.1

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: FR

Effective date: 19960229

REG Reference to a national code

Ref country code: FR

Ref legal event code: ST

REG Reference to a national code

Ref country code: FR

Ref legal event code: ST

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: AT

Effective date: 19960525

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: DE

Effective date: 19970201