US3131058A - Method of manufacturing fine grained and clean steels - Google Patents

Method of manufacturing fine grained and clean steels Download PDF

Info

Publication number
US3131058A
US3131058A US177425A US17742562A US3131058A US 3131058 A US3131058 A US 3131058A US 177425 A US177425 A US 177425A US 17742562 A US17742562 A US 17742562A US 3131058 A US3131058 A US 3131058A
Authority
US
United States
Prior art keywords
steels
alloy
fine grained
steel
carbon
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
US177425A
Inventor
Ototani Tohei
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.)
RES INST IRON STEEL
RESEARCH INSTITUTE FOR IRON
Original Assignee
RES INST IRON STEEL
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 RES INST IRON STEEL filed Critical RES INST IRON STEEL
Priority to US177425A priority Critical patent/US3131058A/en
Application granted granted Critical
Publication of US3131058A publication Critical patent/US3131058A/en
Anticipated expiration legal-status Critical
Expired - Lifetime 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
    • C21C7/0006Adding metallic additives

Definitions

  • the present invention relates to a method of manufacturing ordinary steels of eutectoid and hypo-eutectoid structures containing less than 0.85% carbon and alloy steels containing less than 2.0% carbon and also to such steels and alloy steels manufactured by the method.
  • the method of the invention is characterized in that ordinary steels of eutectoid and hypo-eutectoid structures containing less than 0.85% of C or an alloy steel containing less than 2.0% of C are made to contain 0.0001 to 0.05 of calcium by adding to the melt of the above steels a mixture of one or more elements of Al, Ti, V, Zr, Nb and N together with low carbon manganese-calcium base alloy.
  • the principal object of the invention is to produce ordinary steels and/ or alloy steels having fine grained structure by reducing non-metallic inclusions and having improved toughness, fatigue limit and machinability.
  • the known CaSiaMn alloys used for deoxidizing irons use is made of the low carbon 'Mn-Al-Ca-Si addition alloys which contain 22 to 80% of Mn, 0.2 to 35% of Ca, 0.1 to 60% of Al, less than 10% of Fe and the balance substantially of Si, which is within the range of 2 to A of Mn, and more particularly the alloys may contain in addition alkaline earth metals other than Ca and rare earth elements at an amount of about A of the content of Ca.
  • the above alloys manufactured for commercial purposes contain usually 5 to 6% of iron as impurities.
  • Mn-Al-Ca-Si addition alloys containing higher amount of Mn than the heretofore known Ca-Si-Mn alloy can be manufactured easily.
  • the new alloys have higher specific gravity due to the high Mn-content, the ratio of Mn to Si being 1:2 to 4: 1, while it was 1:3 to 1:7 in the latter alloy and owing to low Si-content the new alloy serves as a very favorable addition agent for refining steels.
  • compositions which are in the molten state at a temperature below about 1,600 C. are limited to only those which contain more quantity of -MnO than that as shown at the point C on the diagram, Where the ratio MnOzSiO is 35:65 (about 1:2). This ratio corresponds to 1:13 in the ratio Mn:Si.
  • the ratio Mn:Si is raised and defined to such an extent that all of the oxide products in the molten steel should be in the liquid state.
  • the known Si-Mn alloys contain a large quantity of C as manganese carbide, yet the alloys of the invention have the specialty that they contain a very small amount of carbon as the alloys are decarbonized by the existence of 0.2 to 35% of Ca.
  • the carbon content of the resulting alloy reduces to 0.25%.
  • the carbon content of an ordinary Si-Mn alloy is 0.9 to 2.5%, whilst the carbon content of the present alloy is within the range of 0.1 to 1%.
  • a desired fine grained and clean steel can be obtained Without effecting the perfect deoxidation and de-sulfurization to such an extent less than 0.001 to 0.005% of oxygen and 0.003 to 0.015% of sulfur, i.e., at more than 0.015% of sulfur content and more than 0.005% of oxygen content,
  • the casting or steel ingot has fine grained and clean structure so that it is not necessary to retain more than 0.05% of Ca.
  • the purpose of previously containing Ce, V, Be, Li, Sr and Mg except Ca in the alloy is to expedite the de-sulfurization and deoxidation at the same time to raise the cleanliness of steel and in the manufacture of the addition alloy, it is more convenient to previously add these elements at an amount less than A of the calcium content.
  • the present invention differs from U.S. Patent 3,000,- 7 31 in that the alloy is added together with one or more elements of Al, Ti, Va, Zr, Nb and the like forced deoxiding agent and nitrogen.
  • the above elements may be previously alloyed with Mn-Ca base all-0y.
  • the method of the invention using the Mn-Al-Ca-Si addition alloy is used together with the known process, for instance, if it is used in parallel to the aluminum process the calcium in the said addition alloy reduces alumina in the melt to produce metallic aluminum and aluminum nitride. Accordingly, by the increase of metallic aluminum and aluminum nitride the grains of steel become considerably refined so that it is more effective if compared with the case when using Mn-Ca base alloy alone.
  • the calcium accelerates the reducing action of alumina in the melt and the deoxidizing action, and simultaneously improves the cleanliness of steel.
  • the method of the invention can be applied to ordinary steels containing less than 0.85% of C and alloy steels containing less than 2.0% of C, that is, the invention can be eifectively applied to ordinary steel-s of eutectoid and hypo-eutectoid structure naturally and also the alloy steels containing less than 2.0% of C and one or more of special elements, such as, Si, Mn, Ni, Co, Cr, Cu, Al, W, Mo, V, Ti and Zr.
  • the steel subjected to the above treatment has fine grained and clean structure and its elongation and the reduction of area increase Without substantial change in the strength and also the notched impact value increases considerably and at the same time the machinability is improved and the remarkable improvement in mechanical properties is recognized especially in quenched and tempered steels.
  • Example 1 A steel containing 0.6% of carbon was melted in a basic high frequency electric furnace and deoxidized at a temperature of 1,-630 C. with 0.5% term-manganese, 0.2% Si and 0.06% Al. The steel ingot treated with 0.8% of Mn-Ca base alloy (Ca 24.1%) and untreated one were taken as samples and after forged the grain size and grain coarsening temperature were studied, and the following results were obtained:
  • a process for producing fine grained and clean steels from steels having the composition of carbon steels with less than 0.85% carbonand'having upon solidification entectoid and hypoeutectoid structures and alloy steels containing up to 2% carbon the Steps which comprise adding to a melt of the steels which contain after preliminary deoxidation with manganese and silicon 0.001- 0.3% of the elements selected from the group consisting of Ti, V, Zr, and Nb together with N in an amount of 0.001 to 0.3% and then adding an alloy consisting essentially of 22%80% Mn, 0.2 to 35% Ca, 0.1 to Al, less than 10% Fe and the balance substantially Si, wherein Si is within the range of 2 to A of Mn, said alloy being in an amount sufficient to leave 0001-005 Ca in thesteel, thereby forming a nitride of said group and producing said clean and fine grained steel.

Description

A ril 28, 1964 TOHEI OTOTANI 3,131,058
METHOD OF MANUFACTURING FINE GRAINED AND CLEAN STEELS Filed March 5, 1962 Binar dia ram of Nn0mi0z United States Patent hoe 3,131,058 METHOD OF MANUFACTURING FINE GRAINED AND CLEAN STEELS Tohei Ototani, Kawauchi, Sendai City, Japan, assignor to The Research Institute for Iron, Steel and Other Metals of The Tohoku University, Sendai City, Japan Filed Mar. 5, 1962, Ser. No. 177,425 2 Claims. (Cl. 75-129) The present invention relates to a method of manufacturing ordinary steels of eutectoid and hypo-eutectoid structures containing less than 0.85% carbon and alloy steels containing less than 2.0% carbon and also to such steels and alloy steels manufactured by the method.
The method of the invention is characterized in that ordinary steels of eutectoid and hypo-eutectoid structures containing less than 0.85% of C or an alloy steel containing less than 2.0% of C are made to contain 0.0001 to 0.05 of calcium by adding to the melt of the above steels a mixture of one or more elements of Al, Ti, V, Zr, Nb and N together with low carbon manganese-calcium base alloy.
The principal object of the invention is to produce ordinary steels and/ or alloy steels having fine grained structure by reducing non-metallic inclusions and having improved toughness, fatigue limit and machinability.
It has heretofore been known in the art that the control of the size of the grain in steels is attained by adding a suitable quantity of one or more elements of Al, Ti, V, Zr and the like elements, and as the cleanliness of steel is effected by the deoxidation and the resultant oxides, a small quantity of Al was added after the deoxidation by means of Mn and Si.
The known CaSiaMn alloys used for deoxidizing irons On the other hand, in accordance with the invention use is made of the low carbon 'Mn-Al-Ca-Si addition alloys which contain 22 to 80% of Mn, 0.2 to 35% of Ca, 0.1 to 60% of Al, less than 10% of Fe and the balance substantially of Si, which is within the range of 2 to A of Mn, and more particularly the alloys may contain in addition alkaline earth metals other than Ca and rare earth elements at an amount of about A of the content of Ca. The above alloys manufactured for commercial purposes contain usually 5 to 6% of iron as impurities.
According to the invention, it has been found that Mn-Al-Ca-Si addition alloys containing higher amount of Mn than the heretofore known Ca-Si-Mn alloy can be manufactured easily. The new alloys have higher specific gravity due to the high Mn-content, the ratio of Mn to Si being 1:2 to 4: 1, while it was 1:3 to 1:7 in the latter alloy and owing to low Si-content the new alloy serves as a very favorable addition agent for refining steels.
For a better understanding of the invention reference is taken to the accompanying drawing, a single figure of which illustrates the binary state diagram of MnO and SiO;;,.
Re-fern'ng to the drawing, the compositions which are in the molten state at a temperature below about 1,600 C. are limited to only those which contain more quantity of -MnO than that as shown at the point C on the diagram, Where the ratio MnOzSiO is 35:65 (about 1:2). This ratio corresponds to 1:13 in the ratio Mn:Si.
It is apparent from the drawing that when an alloy in 3,131,058 Patented Apr. 28, 1964 which the ratio of Mn to Si is more than 1:13 is added to a steel the resultant oxides, i.e., non-metallic inclusion in the steel produced by the alloy has the composition which should be in a molten state at a temperature below 1,600 C.
According to the invention, if compared with known Si-tMn-Ca alloys, the ratio Mn:Si is raised and defined to such an extent that all of the oxide products in the molten steel should be in the liquid state. Moreover, though the known Si-Mn alloys contain a large quantity of C as manganese carbide, yet the alloys of the invention have the specialty that they contain a very small amount of carbon as the alloys are decarbonized by the existence of 0.2 to 35% of Ca.
If, for instance, about 7.5% of Ca is added to a melt of Si-Mn alloy containing 1.2% of C, 20% of Si and 61% of Mn, the carbon content of the resulting alloy reduces to 0.25%. The carbon content of an ordinary Si-Mn alloy is 0.9 to 2.5%, whilst the carbon content of the present alloy is within the range of 0.1 to 1%.
In carrying out the method of the invention, a desired fine grained and clean steel can be obtained Without effecting the perfect deoxidation and de-sulfurization to such an extent less than 0.001 to 0.005% of oxygen and 0.003 to 0.015% of sulfur, i.e., at more than 0.015% of sulfur content and more than 0.005% of oxygen content,
if a suitable quantity of Al, Ti, V, Zr, Nb and nitrogen is retained and if the retained quantity of Ca is more than 0.0001% the casting or steel ingot has fine grained and clean structure so that it is not necessary to retain more than 0.05% of Ca. The purpose of previously containing Ce, V, Be, Li, Sr and Mg except Ca in the alloy is to expedite the de-sulfurization and deoxidation at the same time to raise the cleanliness of steel and in the manufacture of the addition alloy, it is more convenient to previously add these elements at an amount less than A of the calcium content.
The present invention differs from U.S. Patent 3,000,- 7 31 in that the alloy is added together with one or more elements of Al, Ti, Va, Zr, Nb and the like forced deoxiding agent and nitrogen. One or more of the above elements may be previously alloyed with Mn-Ca base all-0y.
After deoxidation by means of manganese and silicon in the final refining period of molten steel, 0.001 to 0.3% of N and Al, Ti, Va, Zr and the like elements to be added as a small quantity of forced deoxidizing agent combines with oxygen in the melt and a part forms a compound and another part forms nitride and the remaining is alloyed with the melt. If, however, the elements of these forced deoxidizing agents are contained in the MnAl-Ca-Si addition alloy such elements act more effectively on the melt so that it is sufiicient to use /2 to /3 the quantity of the former deoxidizing agent if used alone. Only in this case Mn-Al-Ca-Si addition alloy is added without said forced deoxidizing elements.
According to the invention, it has been found that if the method of the invention using the Mn-Al-Ca-Si addition alloy is used together with the known process, for instance, if it is used in parallel to the aluminum process the calcium in the said addition alloy reduces alumina in the melt to produce metallic aluminum and aluminum nitride. Accordingly, by the increase of metallic aluminum and aluminum nitride the grains of steel become considerably refined so that it is more effective if compared with the case when using Mn-Ca base alloy alone.
Further, according to the invention, the calcium accelerates the reducing action of alumina in the melt and the deoxidizing action, and simultaneously improves the cleanliness of steel.
The method of the invention can be applied to ordinary steels containing less than 0.85% of C and alloy steels containing less than 2.0% of C, that is, the invention can be eifectively applied to ordinary steel-s of eutectoid and hypo-eutectoid structure naturally and also the alloy steels containing less than 2.0% of C and one or more of special elements, such as, Si, Mn, Ni, Co, Cr, Cu, Al, W, Mo, V, Ti and Zr.
The steel subjected to the above treatment has fine grained and clean structure and its elongation and the reduction of area increase Without substantial change in the strength and also the notched impact value increases considerably and at the same time the machinability is improved and the remarkable improvement in mechanical properties is recognized especially in quenched and tempered steels. I
The invention will be explained further in detail with examples.
Example 1 A steel containing 0.6% of carbon was melted in a basic high frequency electric furnace and deoxidized at a temperature of 1,-630 C. with 0.5% term-manganese, 0.2% Si and 0.06% Al. The steel ingot treated with 0.8% of Mn-Ca base alloy (Ca 24.1%) and untreated one were taken as samples and after forged the grain size and grain coarsening temperature were studied, and the following results were obtained:
Steel containing 0.82% was melted in a basic high frequency electric furnace and after deoxidation wit-h 0.5% Mn and 0.2% Si at 1,620 c. the molten steel 4 was divided into 2 portions, to one of which was added 4 0.8% of Mn-Ca base alloy (Ca 24.8%, A1 3.2%) and to the other 0.05% of Al and after casting the samples were forged and the grain size was tested and obtained the following results:
What I claim is:
1. A process for producing fine grained and clean steels from steels having the composition of carbon steels with less than 0.85% carbonand'having upon solidification entectoid and hypoeutectoid structures and alloy steels containing up to 2% carbon, the Steps which comprise adding to a melt of the steels which contain after preliminary deoxidation with manganese and silicon 0.001- 0.3% of the elements selected from the group consisting of Ti, V, Zr, and Nb together with N in an amount of 0.001 to 0.3% and then adding an alloy consisting essentially of 22%80% Mn, 0.2 to 35% Ca, 0.1 to Al, less than 10% Fe and the balance substantially Si, wherein Si is within the range of 2 to A of Mn, said alloy being in an amount sufficient to leave 0001-005 Ca in thesteel, thereby forming a nitride of said group and producing said clean and fine grained steel.
2. A method of manufacturing fine grained and clean steels according to claim 1, which comprises using said Mn-Al, Ca-Si addition alloy containing rare earth metals and alkaline earth metals other than calcium at an amount less than A of the calcium content.
References Cited in the file of this patent UNITED STATES PATENTS 2,291,842 Strauss Aug. 4, 1942 2,370,389 Chandler Feb. 27, i945 3,000,731 Ototani Sept. 19, 1961

Claims (1)

1. A PROCESS FOR PRODUCING FINE GRAINED AND CLEAN STEELS FROM STEELS HAVING THE COMPOSITION OF CARBON STEELS WITH LESS THAN 0.85% CARBON AND HAVING UPON SOLIDIFICATION EUTECTOID AND HYPOEUTECTOID STRUCTURES AND ALLOY STEELS CONTAINING UP TO 2% CARBON, THE STEPS WHICH COMPRISE ADDING TO A MELT OF THE STEELS WHICH CONTAIN AFTER PRELIMINARY DEOXIDATION WITH MANGANESE AND SILICON 0.0010.3% OF THE ELEMENTS SELECTED FROM THE GROUP CONSISTING OF TI, V, ZR, AND NB TOGETHER WITH N IS AN AMOUNT JOF 0.001 TO 0.3% AND THEN ADDING AN ALLOY CONSISTING ESSENTIALLY OF 22%-80% MN, J0.2 TO 35% CA, 0.1 TO 60% AL, LESS THAN 10% FE AND THE BALANCE SUBSTANTIALLY SI, WHEREIN SI IS WITHIN THE RANGE OF 2 TO 1/4 OF MN, SAID ALLOY BEING IN AN AMOUNT SUFFICINET TO LEAVE 0.001-0.05 CA IN THE STEEL, THEREBY FORMING A NITRIDE OF SAID GROUP AND PRODUCING SAID CLEAN AND FINE GRAINED STEEL.
US177425A 1962-03-05 1962-03-05 Method of manufacturing fine grained and clean steels Expired - Lifetime US3131058A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
US177425A US3131058A (en) 1962-03-05 1962-03-05 Method of manufacturing fine grained and clean steels

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US177425A US3131058A (en) 1962-03-05 1962-03-05 Method of manufacturing fine grained and clean steels

Publications (1)

Publication Number Publication Date
US3131058A true US3131058A (en) 1964-04-28

Family

ID=22648550

Family Applications (1)

Application Number Title Priority Date Filing Date
US177425A Expired - Lifetime US3131058A (en) 1962-03-05 1962-03-05 Method of manufacturing fine grained and clean steels

Country Status (1)

Country Link
US (1) US3131058A (en)

Cited By (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3364015A (en) * 1963-06-24 1968-01-16 Grace W R & Co Silicon alloys containing rare earth metals
US3383202A (en) * 1966-01-19 1968-05-14 Foote Mineral Co Grain refining alloy
US3540882A (en) * 1967-07-24 1970-11-17 Res Inst Iron Steel Metal refining agent consisting of al-mn-ca alloy
US3649253A (en) * 1968-10-14 1972-03-14 Sueddeutsche Kalkstickstoff Deoxidation of aluminum-killed molten steel
US3951645A (en) * 1974-08-16 1976-04-20 Jones & Laughlin Steel Corporation Steelmaking practice for production of a virtually inclusion-free semi-killed product
DE2830850A1 (en) * 1977-07-13 1979-02-01 Carpenter Technology Corp CASE-ALLOY STEEL
US6077326A (en) * 1997-07-01 2000-06-20 Rock Creek Aluminum Steel additive for processing molten steel
US20040109784A1 (en) * 2001-04-04 2004-06-10 Alireza Arbab Steel and steel tube for high- temperature use
US20110044845A1 (en) * 2008-04-22 2011-02-24 Vitatech GmbH 'kazakhstanskiy' alloy for steel deoxidation and alloying

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2291842A (en) * 1940-07-18 1942-08-04 Vanadium Corp Production of steel
US2370389A (en) * 1941-05-06 1945-02-27 Harold E Bessin Art of taking impressions of eyeballs
US3000731A (en) * 1958-02-03 1961-09-19 Res Inst Iron Steel Fine-grained steels

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2291842A (en) * 1940-07-18 1942-08-04 Vanadium Corp Production of steel
US2370389A (en) * 1941-05-06 1945-02-27 Harold E Bessin Art of taking impressions of eyeballs
US3000731A (en) * 1958-02-03 1961-09-19 Res Inst Iron Steel Fine-grained steels

Cited By (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3364015A (en) * 1963-06-24 1968-01-16 Grace W R & Co Silicon alloys containing rare earth metals
US3383202A (en) * 1966-01-19 1968-05-14 Foote Mineral Co Grain refining alloy
US3540882A (en) * 1967-07-24 1970-11-17 Res Inst Iron Steel Metal refining agent consisting of al-mn-ca alloy
US3649253A (en) * 1968-10-14 1972-03-14 Sueddeutsche Kalkstickstoff Deoxidation of aluminum-killed molten steel
US3951645A (en) * 1974-08-16 1976-04-20 Jones & Laughlin Steel Corporation Steelmaking practice for production of a virtually inclusion-free semi-killed product
DE2830850A1 (en) * 1977-07-13 1979-02-01 Carpenter Technology Corp CASE-ALLOY STEEL
US6077326A (en) * 1997-07-01 2000-06-20 Rock Creek Aluminum Steel additive for processing molten steel
US20040109784A1 (en) * 2001-04-04 2004-06-10 Alireza Arbab Steel and steel tube for high- temperature use
US20110044845A1 (en) * 2008-04-22 2011-02-24 Vitatech GmbH 'kazakhstanskiy' alloy for steel deoxidation and alloying
US8795587B2 (en) * 2008-04-22 2014-08-05 RSE the National Center on Complex Processing of Mineral Raw Material of the Republic Kazakhstan ‘Kazakhstanskiy’ alloy for steel deoxidation and alloying

Similar Documents

Publication Publication Date Title
JP3512873B2 (en) High life induction hardened bearing steel
JPH083682A (en) High carbon type long life bearing steel
JP3294245B2 (en) High carbon steel wire with excellent drawability and fatigue resistance after drawing
US3131058A (en) Method of manufacturing fine grained and clean steels
JPH08193247A (en) Carburized bearing steel with long service life
US3000731A (en) Fine-grained steels
JPH09157787A (en) High tensile strength steel for welding excellent in toughness in very large heat input welded heat affected zone
JPH07188847A (en) Machine-structural carbon steel excellent in machiniability
US3178318A (en) Process for producing nonageing super deep-drawing steel sheets
US2537103A (en) Production of nitrogen-bearing stainless steel
JPH08325635A (en) Production of high strength and high toughness steel excellent in hic resistance
US3304174A (en) Low oxygen-silicon base addition alloys for iron and steel refining
JP2991796B2 (en) Melting method of thin steel sheet by magnesium deoxidation
RU2337148C2 (en) Band out of medium carbon boron containing steel of upgraded hardenability and cutability
JP3537685B2 (en) Slab for thin steel sheet with less inclusion defect and method for producing the same
JP3757633B2 (en) Steel plate for cans with excellent workability
CN112789363B (en) Non-oriented electrical steel sheet and method for producing slab cast sheet as material thereof
US3119688A (en) Manganese aluminum alloy for deoxidizing steel
JPS6234801B2 (en)
CN115491569B (en) Production method of non-oriented silicon steel and non-oriented silicon steel
US2316948A (en) Aluminum-treated cast steel
JPH08193245A (en) Bearing steel and its production
JPH0726175B2 (en) Method for manufacturing high speed tool steel
JP3653990B2 (en) Hot rolled steel sheet with extremely good secondary work brittleness resistance after ultra deep drawing
US3540882A (en) Metal refining agent consisting of al-mn-ca alloy