US3717456A - Alloy and method for treatment to produce spheroidal-graphite cast irons - Google Patents

Alloy and method for treatment to produce spheroidal-graphite cast irons Download PDF

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Publication number
US3717456A
US3717456A US00121178A US3717456DA US3717456A US 3717456 A US3717456 A US 3717456A US 00121178 A US00121178 A US 00121178A US 3717456D A US3717456D A US 3717456DA US 3717456 A US3717456 A US 3717456A
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United States
Prior art keywords
weight
treatment
alloy
cast iron
iron
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Expired - Lifetime
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US00121178A
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English (en)
Inventor
J Percheron
L Septier
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Pechiney SA
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Pechiney SA
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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
    • C21C1/00Refining of pig-iron; Cast iron
    • C21C1/10Making spheroidal graphite cast-iron
    • C21C1/105Nodularising additive agents
    • 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
    • C21C1/00Refining of pig-iron; Cast iron
    • 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
    • C21C1/00Refining of pig-iron; Cast iron
    • C21C1/10Making spheroidal graphite cast-iron
    • 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

  • This invention relates to an alloy for the treatment of spheroidal-graphite cast irons.
  • the conventional two-stage treatment often produces unsatisfactory results.
  • it has to be completed by a heat treatment of the solid metal, namely by annealing above the Ac point.
  • annealing gives rise to surface faults which, in turn, produce such tensions, especially in the case of castings having zones of highly variable thickness, that permanent deformations occur.
  • the use of the alloy, according to the invention thus affords a number of advantages. It simplifies the handling of and reduces the losses of heat from the liquid pig iron. The losses of magnesium are reduced, thus allowing substantial quantities of this nodularizing element to be saved and much tighter control of its final content. It is known that magnesium stabilizes carbides thereby increasing the fragile/ductile transition temperature of the cast iron with the result that its content has to be adjusted to the minimum compatible with effective nodularization. On the other hand, it is no longer necessary to adjust the silicon content of the cast iron by the addition of expensive silicon-based alloys after it has been nodularized with magnesium. This is because, by virtue of the novel additional alloys, it is possible to adjust the silicon content in the blast furnace or in the cupola furnace by means of less expensive starting materials.
  • the additive alloy of the present invention is of the Fe-Si-Mg type and contains the Ba-N couple, the nitrogen being introduced, for example, by bubbling.
  • the composition is as follows:
  • the alloy is further characterized by a ratio by weight of MgzBa of 1 part by weight Mg to l-3 parts by weight Ba.
  • the various constituents of the alloy of the invention are balanced to produce not only a ferrite matrix, but also a uniformity in the size of the spheroids precipitated and a level of resistance to the formation of troublesome elements (especially carbide formers) which is reflected in the tolerance, during manufacture of the cast iron, of a recycling rate (introduction of scrap and returns) which can reach 50% and higher.
  • the alloy of this invention is characterized by the following:
  • quantity of alloy to be used is such that the magnesium is usually present in a quantity of from 0.08 to 0.3% of the weight of the cast iron to be treated.
  • cast irons can be nodularized with additive alloys of the Fe-Si-Mg-Ca-N type in which some of the nitrogen is present in the form of a suspension of calcium cyanarnide.
  • A treatment with an alloy according to the invention
  • B- substantially identical treatment except that the alloy contains Ca instead of Ba and then a quantity, equivalent to approximately 0.8% of the weight of the cast iron obtained, of an inoculating alloy which is a ferrosilicon with a silicon content of 75%.
  • the three comparative treatments with alloys A, B and C are carried out on the same basic cast iron made in an induction furnace. Three batches of 600' kg. each are removed from the furnace for each of the treatments described.
  • the temperature of the cast iron during treatments A, B and C is between 1480 C. and 1520 C.
  • the castings and the control specimens are produced at the end of ladle casting
  • the period of time elapsing between the treatment and casting of the specimens under examination was between 10 and 15 minutes.
  • Tables 1 and 2 give the results obtained from micrographic structural examinations and from mechanical tests on the crude cast metal.
  • Liquid cast iron is made in an acid cupola from a batch comprising 50% of new cast iron and 50% of scrap castings, being subsequently desulphurized with CaC by known methods.
  • the cast iron is then transferred to a holding-type induction furnace. Passage through this holding furnace enables the silicon content of the cast iron to be adjusted before treatment A and B so as to obtain, after treatment, a cast iron having a composition comparable to that of a cast iron which has been subjected to treatment of type C.
  • Treatments A and B comprise introducing, in sandwich" form, into the cast iron to be treated, a quantity of approximately 1.8% by weight of this cast iron of an alloy containing for treatment A:
  • Treatment C comprises introducing in sandwich form into the cast iron to be treated, first a quantity equivalent to about 1.8% by weight of this cast iron of a nodularizing Fe-Si-Mg alloy with 8.10% Mg content containing:
  • EXAMPLE 1 2.250 kg. of a master alloy, representing the practice of this invention, containing, in addition to iron and the usual impurities, 48.2% by weight silicon, 9.1% by weight magnesium, 4.75% by weight barium and 0.4% by weight nitrogen, is introduced by means of a known type of plunger into a ladle containing 75 kg. of cast iron, containing carbon and silicon, maintained at a temperature of 1480" C.
  • the resulting cast iron has the following composition:
  • the castings and the control specimens show a precipitation of perfectly spheroidal graphite. No carbide is present in the castings, even in the thin zones.
  • the matrix has a ferrite content.
  • EXAMPLE 2 4 kg. of a master alloy of this invention containing, in addition to iron and the usual impurities, 47.4% silicon, 5.02% magnesium, 2.70% barium, 0.4% calcium and 0.30% nitrogen, are introduced by means of a plunger into a ladle containing 75 kg. cast iron at a temperature of 1510 C.
  • the cast iron has the following composition:
  • the castings show a precipitation of perfectly spheroidal graphite. No carbide is present in the castings, even in the thin areas.
  • the matrix has a ferrite content of 85 to 90%.
  • EXAMPLE 3 13.2 kg. of a master alloy, containing 49.4% by weight Si, 8.8% Mg, 4.85% Ba, 0.32% Ca, 0.46% N, the remainder to 100% consisting of iron and impurities, are introduced by the so-called sandwich technique into a ladle containing 600 kg. of a cast iron prepared in an arc furnace from a batch comprising 40% of scrap iron and 60% of scrap castings at a temperature of 1480 C. (In the sandwich technique, the mother alloy is initially placed at the bottom of a treatment ladle, covered with scrap iron and then the cast iron to be treated is poured into the ladle.)
  • the cast iron contains 3.55% C, 2.70% Si and 0.058% Mg.
  • EXAMPLE 4 600 kg. of cast iron having a temperature of 1480" C. are treated by the sandwich technique with 25 kg. of a master alloy of the invention, containing 43.2% Si, 3.6% Mg, 15% Ba, 0.19% N, the remainder to 100% consisting of iron and impurities.
  • Casting is finished 12 minutes after the treatment.
  • All the castings obtained consist of spheroidal graphite cast iron. Examination reveals a carbide-free ferrite structure in the crude cast state.
  • the average composition is as follows:
  • the method for treatment to produce spheroidal graphite cast irons comprising introducing into the Cast iron while in the molten state an alloy additive consisting essentially of 4055% by weight Si, 3-15% by weight Mg, 1.48.6% by Weight Ba, nitrogen in an amount to provide a weight ratio of Ba: N within the range of 5-50, the remainder being iron plus impurities.

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  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Metallurgy (AREA)
  • Organic Chemistry (AREA)
  • Refinement Of Pig-Iron, Manufacture Of Cast Iron, And Steel Manufacture Other Than In Revolving Furnaces (AREA)
US00121178A 1970-04-16 1971-03-04 Alloy and method for treatment to produce spheroidal-graphite cast irons Expired - Lifetime US3717456A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
FR7013757A FR2087003A5 (de) 1970-04-16 1970-04-16

Publications (1)

Publication Number Publication Date
US3717456A true US3717456A (en) 1973-02-20

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US00121178A Expired - Lifetime US3717456A (en) 1970-04-16 1971-03-04 Alloy and method for treatment to produce spheroidal-graphite cast irons

Country Status (15)

Country Link
US (1) US3717456A (de)
AT (1) AT312646B (de)
BE (1) BE765645A (de)
BR (1) BR7102266D0 (de)
CA (1) CA935670A (de)
CH (1) CH522737A (de)
ES (1) ES390133A1 (de)
FR (1) FR2087003A5 (de)
GB (1) GB1289925A (de)
IL (1) IL36594A (de)
LU (1) LU62982A1 (de)
NL (1) NL169347C (de)
NO (1) NO127201B (de)
SE (1) SE380291B (de)
ZA (1) ZA712390B (de)

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3977868A (en) * 1974-08-16 1976-08-31 Hitachi, Ltd. Nitrogen containing additive for strengthening cast iron
US4024322A (en) * 1975-03-24 1977-05-17 Hooker Chemicals & Plastics Corporation Battery with silicon metal anodes
US4040821A (en) * 1975-08-22 1977-08-09 Ford Motor Company Nodularizing catalyst for cast iron and method of making same
US4306904A (en) * 1977-10-11 1981-12-22 Societe Francaise D'electrometallurgie Sofrem Process of introducing a solid addition into a bath of liquid metal
US5008074A (en) * 1990-04-26 1991-04-16 American Alloys, Inc. Inoculant for gray cast iron
US20100294452A1 (en) * 2006-07-25 2010-11-25 Foseco International Limited Method of Producing Ductile Iron

Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3977868A (en) * 1974-08-16 1976-08-31 Hitachi, Ltd. Nitrogen containing additive for strengthening cast iron
US4024322A (en) * 1975-03-24 1977-05-17 Hooker Chemicals & Plastics Corporation Battery with silicon metal anodes
US4040821A (en) * 1975-08-22 1977-08-09 Ford Motor Company Nodularizing catalyst for cast iron and method of making same
US4306904A (en) * 1977-10-11 1981-12-22 Societe Francaise D'electrometallurgie Sofrem Process of introducing a solid addition into a bath of liquid metal
US5008074A (en) * 1990-04-26 1991-04-16 American Alloys, Inc. Inoculant for gray cast iron
US20100294452A1 (en) * 2006-07-25 2010-11-25 Foseco International Limited Method of Producing Ductile Iron
US8297340B2 (en) * 2006-07-25 2012-10-30 Foseco International Limited Method of producing ductile iron

Also Published As

Publication number Publication date
BR7102266D0 (pt) 1973-06-12
DE2117776A1 (de) 1971-11-04
CA935670A (en) 1973-10-23
AT312646B (de) 1974-01-10
IL36594A0 (en) 1971-06-23
SE380291B (sv) 1975-11-03
ES390133A1 (es) 1975-02-16
DE2117776B2 (de) 1973-01-04
NL169347C (nl) 1982-07-01
FR2087003A5 (de) 1971-12-31
CH522737A (fr) 1972-06-30
GB1289925A (de) 1972-09-20
LU62982A1 (de) 1972-03-02
NL7104866A (de) 1971-10-19
IL36594A (en) 1973-10-25
BE765645A (fr) 1971-10-13
ZA712390B (en) 1972-01-26
NO127201B (de) 1973-05-21

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