US3158466A - Product for refining effervescent, quiescent and semi-quiescent steel in the casting - Google Patents

Product for refining effervescent, quiescent and semi-quiescent steel in the casting Download PDF

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Publication number
US3158466A
US3158466A US83619A US8361961A US3158466A US 3158466 A US3158466 A US 3158466A US 83619 A US83619 A US 83619A US 8361961 A US8361961 A US 8361961A US 3158466 A US3158466 A US 3158466A
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US
United States
Prior art keywords
steel
quiescent
product
casting
refining
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
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US83619A
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English (en)
Inventor
Muller Guillaume
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.)
Prochirhin SA
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Prochirhin SA
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Filing date
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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
    • C21C7/04Removing impurities by adding a treating agent
    • C21C7/076Use of slags or fluxes as treating agents
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02PCLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
    • Y02P10/00Technologies related to metal processing
    • Y02P10/20Recycling

Definitions

  • the present invention relates to a product for refining effervescent, quiescent and semi-quiescent steel in the casting.
  • traces of refractory material or of lime may be carried along by the molten steel, either into the middle or just underneath the skin of the ingot.
  • bubbles may be produced at such points and form objectionable inclusions which often lead to the production of undesirable lines during subsequent rolling.
  • the steel is subjected to the action of energetically stirred air which saturates the steel ⁇ m'th oxygen which is associated with that of the oxides already contained in the metal.
  • the conventional methods of purification resort to silicon as a purifying agent, in the form of a Fe-Si or Fe-Cr-Si alloy or the like silicon alloy with low carbon contents, or else, to aluminium, or a mixture of silicon and aluminium, or again, to manganese alloyed with iron or in the form of aptaisen.
  • the formation of slags by the inclusions is more marked when the steel is more fluid, that is when it is hotter and when the inclusions are larger.
  • alkaline or the like fluorinated derivatives are used, either in admixture with suitable derivatives of boron, or as chemical combinations with the latter, e.g. in the form of fluoborates, either alone or in association with alkaline or the like hydroborons.
  • a flux such as e.g. fluorides, chiefly sodium, lithium or potassium fluorides and a reducing agent such as carbon, silicon, manganese or aluminium.
  • the reduction is activated by the presence of alkaline carbonates, the basic character of which forms an essential factor for such a reduction.
  • a typical composition of such refining powders is as follows, by weight:
  • the anhydrous alkaline borates are admixed with alka line fluorides by incorporating with the mixture alkaline carbonates and highly subdivided carbon in a stable condition, such as graphite, or else, boric acid is admixed with alkaline fluorides in the presence of alkaline fluxes, or again, alkaline fluorides or the like fluoborates are admixed with fluoboric acid or alkaline or the like fluorides, fluosilicates or fluotitanates.
  • the alkaline derivatives may be replaced entirely or partly by fluorides of rare earth elements, such as cerium fluoride, fluoborate or fluosilicate.
  • the carbon may be replaced in the above mixtures, either partly or entirely, by elements of the fourth group of Mendeleevs Periodic Table. Boron may be replaced similarly in the above mixtures, either totally or partly, by elements of the third group such as titanium.
  • the steels with which the mixture may be incorporated are chiefly effervescent steels, but it may also be incorporated, under certain conditions, with quiescent or semiquiescent steels.
  • the powder tobe incorporated with the steel should, in its most active form, contain a proportion of the solvent and reducing product as high as and even and never underneath these values, so as to prevent the slag formed from showing a too great compacity.
  • the product obtained is introduced into the molten steel in amounts lower than or equal to 0.1 kg. per metric ton, but the conditions of operation may require lowering these amounts down to 0.01 kg, or else, one uses 1 or even 2 kg. per metric ton.
  • a large fraction of the nitrides formed is solubilized in the fluid slag produced under the action of the refining powder and the boronitrides, formed during operation and which are stable up to 2,000 C., modify substantially the crystalline structure and lead to a clear improvement in the grade of the steel, this being due, in particular, to a substantial increase in the mechanical resistance of the latter.
  • the product may be added, either by a shovel, at the moment of the casting in a ladle orin an ingot mold, or else, it maybe introduced inside gauged cardboard boxes, each of which contains an accurate weight of the product adapted for the casting conditions and the grade of the steel. It may also be carried by blisterpreventing cardboards, generally positioned at the bottom of the ingot mold, before the casting, and this increases not only the protective action of these cardboards, but also forms a reliable safeguard, whereby one makes sure the product has been actually added at the proper moment during the casting. Lastly, it allows obtaining through adjustment of the length of the cardboard introduced into the ingot mold, the automatic measurement of the product in accordance with the size of the block.
  • Example 1 22 metric tons of mild steel are treated with 120 kg.
  • Example 2 50 metric tons of steel for strip iron are treated with 250 kg. of an alloy of Fe-Mn and 30 kg. of anthracite and there is added at the moment of the casting 1,000 gr. of the same refining powder into an ingot mold for ingets of 7 tons.
  • Total waste treated steel 2.9%; non-treated steel 13%.
  • said contents are lowered from 0.015% down to 0.004% through a treatment of 25 tons of steel by 50 kg. of the refining powder.
  • the steels treated in accordance with the present invention may be considered as more highly refined from all points of view.
  • An alkaline refining product for steel adapted to be incorporated into said steel during its casting at a ratio of 0.01 kg. to 2 kg. per metric ton
  • said alkaline refining product consisting of a mixture about of anhydrous borax, about 10% of sodium fluoride,

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)
  • Continuous Casting (AREA)
US83619A 1960-01-21 1961-01-19 Product for refining effervescent, quiescent and semi-quiescent steel in the casting Expired - Lifetime US3158466A (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
FR6841A FR1245440A (fr) 1960-01-21 1960-01-21 Produits d'affinage pour aciers effervescents, calmés ou semi-calmés
FR6915A FR77793E (fr) 1960-01-21 1960-05-25 Produits d'affinage pour aciers effervescents, calmés ou semi-calmés

Publications (1)

Publication Number Publication Date
US3158466A true US3158466A (en) 1964-11-24

Family

ID=35615539

Family Applications (1)

Application Number Title Priority Date Filing Date
US83619A Expired - Lifetime US3158466A (en) 1960-01-21 1961-01-19 Product for refining effervescent, quiescent and semi-quiescent steel in the casting

Country Status (5)

Country Link
US (1) US3158466A (de)
BE (1) BE599338A (de)
DE (1) DE1408878C3 (de)
FR (2) FR1245440A (de)
GB (1) GB979427A (de)

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3436209A (en) * 1966-10-31 1969-04-01 Metallurg Exoproducts Corp Production of rimmed steels
US3639117A (en) * 1970-05-14 1972-02-01 Bethlehem Steel Corp Method for producing bearing grade alloy steels
US4189316A (en) * 1978-01-30 1980-02-19 Tulsky Proektno-Konstruktorsky Tekhnologichesky Institut Mashinostroenia Iron modifier and method of using same
US4224063A (en) * 1979-04-26 1980-09-23 Peregudov Lev V Method of using iron modifier
US4314847A (en) * 1980-06-23 1982-02-09 Nisshin Steel Company, Ltd. Process for dephosphorization and denitrification of chromium-containing iron

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4869749A (en) * 1988-11-23 1989-09-26 Air Products And Chemicals, Inc. Chemical dehydrogenation of molten ferrous alloys using a halogen-containing compound

Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US1975084A (en) * 1932-03-07 1934-10-02 Davies Edith Vail Composition of matter and process of treating molten metals
US2173205A (en) * 1936-12-28 1939-09-19 Roechlingsche Eisen & Stahl Process for the deoxidation of steel baths
US2196853A (en) * 1938-10-27 1940-04-09 Special Chemicals Corp Flux composition
US2357014A (en) * 1941-07-07 1944-08-29 William L Ulmer Flux composition
US2829078A (en) * 1955-05-19 1958-04-01 Henry B Aull Flux composition
US2932564A (en) * 1957-06-21 1960-04-12 Norman R Evans Mica treated metals

Patent Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US1975084A (en) * 1932-03-07 1934-10-02 Davies Edith Vail Composition of matter and process of treating molten metals
US2173205A (en) * 1936-12-28 1939-09-19 Roechlingsche Eisen & Stahl Process for the deoxidation of steel baths
US2196853A (en) * 1938-10-27 1940-04-09 Special Chemicals Corp Flux composition
US2357014A (en) * 1941-07-07 1944-08-29 William L Ulmer Flux composition
US2829078A (en) * 1955-05-19 1958-04-01 Henry B Aull Flux composition
US2932564A (en) * 1957-06-21 1960-04-12 Norman R Evans Mica treated metals

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3436209A (en) * 1966-10-31 1969-04-01 Metallurg Exoproducts Corp Production of rimmed steels
US3639117A (en) * 1970-05-14 1972-02-01 Bethlehem Steel Corp Method for producing bearing grade alloy steels
US4189316A (en) * 1978-01-30 1980-02-19 Tulsky Proektno-Konstruktorsky Tekhnologichesky Institut Mashinostroenia Iron modifier and method of using same
US4224063A (en) * 1979-04-26 1980-09-23 Peregudov Lev V Method of using iron modifier
US4314847A (en) * 1980-06-23 1982-02-09 Nisshin Steel Company, Ltd. Process for dephosphorization and denitrification of chromium-containing iron

Also Published As

Publication number Publication date
DE1408878A1 (de) 1968-12-12
FR1245440A (fr) 1960-11-04
DE1408878C3 (de) 1975-07-17
BE599338A (fr) 1961-05-16
FR77793E (fr) 1962-04-20
GB979427A (en) 1965-01-06

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