WO2001044530A1 - New alloy and method for producing same - Google Patents

New alloy and method for producing same Download PDF

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Publication number
WO2001044530A1
WO2001044530A1 PCT/SE2000/002550 SE0002550W WO0144530A1 WO 2001044530 A1 WO2001044530 A1 WO 2001044530A1 SE 0002550 W SE0002550 W SE 0002550W WO 0144530 A1 WO0144530 A1 WO 0144530A1
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WO
WIPO (PCT)
Prior art keywords
cast iron
magnesium
inclusions
alloy according
sulfide
Prior art date
Application number
PCT/SE2000/002550
Other languages
French (fr)
Inventor
Wolfgang Troschel
Ralf TÖLLER
Original Assignee
Sintercast Ab
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
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Application filed by Sintercast Ab filed Critical Sintercast Ab
Priority to DE60003952T priority Critical patent/DE60003952T2/en
Priority to KR1020027007747A priority patent/KR20020062761A/en
Priority to US10/149,653 priority patent/US7081151B2/en
Priority to JP2001545607A priority patent/JP2003517099A/en
Priority to AU25639/01A priority patent/AU2563901A/en
Priority to EP00989092A priority patent/EP1252353B1/en
Publication of WO2001044530A1 publication Critical patent/WO2001044530A1/en

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Classifications

    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22CALLOYS
    • C22C37/00Cast-iron alloys
    • C22C37/04Cast-iron alloys containing spheroidal graphite
    • 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
    • C21C1/08Manufacture of 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
    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22CALLOYS
    • C22C33/00Making ferrous alloys
    • C22C33/08Making cast-iron alloys
    • C22C33/10Making cast-iron alloys including procedures for adding magnesium
    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22CALLOYS
    • C22C37/00Cast-iron alloys
    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22CALLOYS
    • C22C37/00Cast-iron alloys
    • C22C37/10Cast-iron alloys containing aluminium or silicon

Definitions

  • the present invention relates to a novel magnesium-treated cast iron containing inclusions, preferably manganese sulfide (MnS) or molybdenium sulfide (MoS 2 ) inclusions.
  • the invention also relates to a procedure for preparing the novel cast iron, cast iron products comprising the novel cast iron, as well as using the novel iron for manufacturing cylinder blocks, cylinder heads, bedplates, transmission housings, axle housings or brake drums and discs.
  • Magnesium treated cast irons such as compacted graphite iron (CGI) and ductile cast iron (SG) are widely used for a variety of applications. Unfortunately, however, in comparison to conventional grey cast iron these alloys are relatively difficult to machine. This factor has prevented their application to many high volume products which require large amounts of machining.
  • CGI compacted graphite iron
  • SG ductile cast iron
  • CGI and SG Although the higher strength, stiffness and ductility of CGI and SG relative to conventional grey cast irons accounts for much the difference in machinability between these materials, other factors may also be active.
  • One such factor is the presence of 1-5 ⁇ m diameter manganese sulfide (MnS) inclusions in grey cast iron. These inclusions are known to adhere to the cutting edge of the machining tools, thus forming a protective layer and reducing tool wear. The effect is particularly significant at high cutting speeds (400-1 000 m/min) when using cubic boron nitride (CBN) or ceramic cutting materials. It is also known that high sulfur and manganese additions improve the machinability of steels. Such steel alloys are referred to in the trade as "free-machining steels".
  • the mechanism for improved machinability relates to the formation of a protective MnS layer on the cutting insert and/or a lubricating effect of the sulfide inclusions between the cutting insert and the workpiece and/or chip.
  • manganese sulfide inclusions are not stable in magnesium-treated cast irons due to the lower free-energy of magnesium sulfide at ironmaking temperatures ( Figure 1). Therefore, a previous patent (SE 9800750-3), incorporated by reference, disclosed a method to convert the existing MgO.Si0 2 inclusions in magnesium-treated cast irons to soft calcium-bearing inclusions.
  • MnS and MoS 2 are not stable in the presence of magnesium.
  • said cast iron can also be formed by adding said sulfides directly to the iron after the magnesium reaction has taken place and an in situ equilibrium has been established between magnesium , oxygen and sulfur. Another option is to begin with a sulfur content in excess of the stoichiometric amount required to combine with the added magnesium, thus ensureing an amount of left-over sulfur to promote the formation of the desired sulfide inclusions.
  • inclusion-fo ⁇ ning compound generally relates to all non-metallic non-organic compounds with hexagonal or face-centred cubic crystal structures and melting points of at least 1100 °C.
  • manganese sulfide or molybdenium sulfide is used in relation to the present invention.
  • the present invention relates to a magnesium-treated cast iron containing inclusions which either lubricate the cutting insert or contribute to the formation of a protective layer on the cutting edge of the insert.
  • the inclusions preferably consist of manganese sulfide (MnS) or molybdenium sulfide (MoS 2 ).
  • the sulfides are added to a molten base iron as 1 - 100 ⁇ m particles. In the presence of heat (1400 - 1500 °C), these particles will become individual spheroids with a uniformly distributed by the convection currents present in the molten iron.
  • This base iron is then treated with magnesium at the last possible moment, preferably when the molten cast iron has been poured into a mould.
  • the present invention will be disclosed with reference to the enclosed figure 1 which shows temperature dependencies of free precipitation energies ⁇ G S ° for some oxides, sulfides, oxysulfides, nitrides and carbides in molten iron.
  • reaction [1] proceeds rapidly to the right. It is therefore important to delay reaction [1] until the last possible moment to prevent reduction of the desired MnS inclusions.
  • the magnesium addition be made as late as possible, preferably just before the iron is dispensed into the mould or in-the-mould itself.
  • the present invention requires that the molten cast iron is not treated with magnesium until the last possible moment before casting.
  • the magnesium can be added immediately before dispensing the molten iron into the mould, but preferably the magnesium is added to the melt after dispensing the molten iron into the mould.
  • the amount of magnesium added in this step is calibrated in advance. Typically the magnesium content of the final cast iron melt is 0.001 - 0.030% (wt).
  • MnS particles or other known solid lubricant particles, such as MoS 2
  • a post-addition of MnS particles, or other known solid lubricant particles, such as MoS 2 may be made to the iron after the magnesium reaction has taken place and an in-situ equilibrium has been established between magnesium, oxygen and sulfur. This will allow the MnS or MoS 2 particles to remain in the solidified casting.
  • 1 - 100 ⁇ m manganese sulfide particles of are added.
  • the addition of these particles result in an amount of manganese in the final melt of at least 0.1 % (wt), and typically about 0.6 %.
  • An amount of of about 4 kg manganese sulfide per tonne molten cast iron is typically added, corresponding to
  • a proposed composition for such a master alloy for adding either MnS or MoS 2 particles is as follows:
  • this alternative method comprises the steps of a) preparing a molten base iron according toper se known methods; b) adding a predetermined amount of magnesium to the molten base iron and allowing establishment of an equilibrium between magnesium, oxygen and sulfur; c) adding a predetermined amount of manganese sulfide and/or molybdenium sulfide; and finally d) casting the melt according to per se known methods.
  • a final option for the stabilisation of MnS in the standard CGI or SG base iron is to increase the sulfur content beyond the typical level of 0.005 - 0.020 % S. In this way , the higher amount of sulfur increases the probability that MnS will form, and indeed survive until the moment of solidification. Thus, the presence of 0.04 % sulfur or more, in the CGI or SG base iron has been shown to result in the presence of MnS inclusions in the final cast products, thus improving their machinability.

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  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Metallurgy (AREA)
  • Organic Chemistry (AREA)
  • Mechanical Engineering (AREA)
  • Manufacturing & Machinery (AREA)
  • Refinement Of Pig-Iron, Manufacture Of Cast Iron, And Steel Manufacture Other Than In Revolving Furnaces (AREA)
  • Treatment Of Steel In Its Molten State (AREA)
  • Heat Treatment Of Articles (AREA)

Abstract

It is possible to generate a desirable form (soft, pliable) of sulfide inclusions in magnesium-treated cast irons. Thermodynamically, MnS and MoS2 are not stable in the presence of magnesium. However, by adding magnesium to a cast iron melt containing manganese sulfide/molybdenium sulfide as late as possible, and preferably when the molten cast iron has been dispensed into the mould, such sulfide inclusions may be preserved in magnesium-treated cast irons. Alternatively, said cast iron can also be formed by adding said sulfides directly to the iron after the magnesium reaction has taken place and an in situ equilibrium has been established between magnesium, oxygen and sulfur. Another option is to begin with a sulfur content in excess of the stoichiometric amount required to combine with the added magnesium, thus ensureing an amount of left-over sulfur to promote the formation of the desired sulfide inclusions.

Description

New Alloy and method for producing same
The present invention relates to a novel magnesium-treated cast iron containing inclusions, preferably manganese sulfide (MnS) or molybdenium sulfide (MoS2) inclusions. The invention also relates to a procedure for preparing the novel cast iron, cast iron products comprising the novel cast iron, as well as using the novel iron for manufacturing cylinder blocks, cylinder heads, bedplates, transmission housings, axle housings or brake drums and discs.
Technical background
Magnesium treated cast irons, such as compacted graphite iron (CGI) and ductile cast iron (SG) are widely used for a variety of applications. Unfortunately, however, in comparison to conventional grey cast iron these alloys are relatively difficult to machine. This factor has prevented their application to many high volume products which require large amounts of machining. One example is automotive cylinders blocks.
Although the higher strength, stiffness and ductility of CGI and SG relative to conventional grey cast irons accounts for much the difference in machinability between these materials, other factors may also be active. One such factor is the presence of 1-5 μm diameter manganese sulfide (MnS) inclusions in grey cast iron. These inclusions are known to adhere to the cutting edge of the machining tools, thus forming a protective layer and reducing tool wear. The effect is particularly significant at high cutting speeds (400-1 000 m/min) when using cubic boron nitride (CBN) or ceramic cutting materials. It is also known that high sulfur and manganese additions improve the machinability of steels. Such steel alloys are referred to in the trade as "free-machining steels". Again, the mechanism for improved machinability relates to the formation of a protective MnS layer on the cutting insert and/or a lubricating effect of the sulfide inclusions between the cutting insert and the workpiece and/or chip. Unfortunately, manganese sulfide inclusions are not stable in magnesium-treated cast irons due to the lower free-energy of magnesium sulfide at ironmaking temperatures (Figure 1). Therefore, a previous patent (SE 9800750-3), incorporated by reference, disclosed a method to convert the existing MgO.Si02 inclusions in magnesium-treated cast irons to soft calcium-bearing inclusions. However, there are no available methods for producing a magnesium-treated cast iron alloy containing soft and pliable inclusions.
Summary of the invention
Now, it has surprisingly turned out that it is possible to generate a desirable form (soft, pliable) of sulfide inclusions in magnesium-treated cast irons. Thermodynamically, MnS and MoS2 are not stable in the presence of magnesium. However, by adding magnesium to a cast iron melt containing manganese sulfide/molybdenium sulfide as late as possible, and preferably when the molten cast iron has been dispensed into the mould, such sulfide inclusions may be preserved in magnesium-treated cast irons. Alternatively, said cast iron can also be formed by adding said sulfides directly to the iron after the magnesium reaction has taken place and an in situ equilibrium has been established between magnesium , oxygen and sulfur. Another option is to begin with a sulfur content in excess of the stoichiometric amount required to combine with the added magnesium, thus ensureing an amount of left-over sulfur to promote the formation of the desired sulfide inclusions.
Detailed description of the invention.
As disclosed herein, the term "inclusion-foπning compound" generally relates to all non-metallic non-organic compounds with hexagonal or face-centred cubic crystal structures and melting points of at least 1100 °C. Preferably manganese sulfide or molybdenium sulfide is used in relation to the present invention. Accordingly, the present invention relates to a magnesium-treated cast iron containing inclusions which either lubricate the cutting insert or contribute to the formation of a protective layer on the cutting edge of the insert. The inclusions preferably consist of manganese sulfide (MnS) or molybdenium sulfide (MoS2). Typically, the sulfides are added to a molten base iron as 1 - 100 μm particles. In the presence of heat (1400 - 1500 °C), these particles will become individual spheroids with a uniformly distributed by the convection currents present in the molten iron. This base iron is then treated with magnesium at the last possible moment, preferably when the molten cast iron has been poured into a mould.
The present invention will be disclosed with reference to the enclosed figure 1 which shows temperature dependencies of free precipitation energies ΔGS° for some oxides, sulfides, oxysulfides, nitrides and carbides in molten iron.
The theory behind the invention is the following: Prior to the addition of magnesium, an equilibrium will have been established between manganese and sulfur in the base iron as a function of the holding temperature. Once the addition of magnesium is made, the stronger sulfide capacity of the magnesium will reduce the MnS according to the reaction:
MnS + Mg = MgS + Mn
ΔG° = -73 kJoules/mol at 1 450°C
The strongly negative free energy and the exothermic nature of the reaction, combined with the small size, high quantity (approximately 10 MnS inclusions per tonne of liquid iron), suggests that reaction [1] proceeds rapidly to the right. It is therefore important to delay reaction [1] until the last possible moment to prevent reduction of the desired MnS inclusions. Thus, it is proposed that the magnesium addition be made as late as possible, preferably just before the iron is dispensed into the mould or in-the-mould itself. The process according to the present invention starts with preparing a molten cast iron according to per se known methods with a typical base iron chemistry for ductile iron and for compacted graphite iron production:
C: 3.5 - 3.9 % S: 0.005 - 0.020 %
Si 1.8 - 2.2 % Mn 0.1 - 0.5 %
The presence of Mn and S in the base iron will naturally lead to the formation of MnS inclusions according to the thermodynamic equilibrium at the holding temperature. Thereafter, in contrast to typical ductile iron and CGI production techniques which may add the magnesium as much as ten minutes before the start- of-pour, the present invention requires that the molten cast iron is not treated with magnesium until the last possible moment before casting. The magnesium can be added immediately before dispensing the molten iron into the mould, but preferably the magnesium is added to the melt after dispensing the molten iron into the mould. In order to minimise formation of magnesium sulfide after the magnesium addition it is also possible to chill the mould filled with molten magnesium-treated and inclusion-containing cast iron, so that the solidification process is accelerated.
The amount of magnesium added in this step is calibrated in advance. Typically the magnesium content of the final cast iron melt is 0.001 - 0.030% (wt).
Alternatively, a post-addition of MnS particles, or other known solid lubricant particles, such as MoS2, may be made to the iron after the magnesium reaction has taken place and an in-situ equilibrium has been established between magnesium, oxygen and sulfur. This will allow the MnS or MoS2 particles to remain in the solidified casting. In this case, 1 - 100 μm manganese sulfide particles of are added. The addition of these particles result in an amount of manganese in the final melt of at least 0.1 % (wt), and typically about 0.6 %. An amount of of about 4 kg manganese sulfide per tonne molten cast iron is typically added, corresponding to
S 1
10 - 10 inclusions per tonne molten cast iron, depending on the efficiency of dissolution and assimilation into the melt. A proposed composition for such a master alloy for adding either MnS or MoS2 particles is as follows:
Si: 0 - 90 % Al: 0 - 10 %
Ca: 0 - 10 % Ba: 0 - 10 %
Sr: 0 - 10 % Zr: 0 - 10 %
Re: 0 - 20 % Mn: 10 - 90 %
MnS: 20 - 70 % MoS2: 20 - 70 %
Fe: 0 - balance.
Accordingly, this alternative method comprises the steps of a) preparing a molten base iron according toper se known methods; b) adding a predetermined amount of magnesium to the molten base iron and allowing establishment of an equilibrium between magnesium, oxygen and sulfur; c) adding a predetermined amount of manganese sulfide and/or molybdenium sulfide; and finally d) casting the melt according to per se known methods.
A final option for the stabilisation of MnS in the standard CGI or SG base iron is to increase the sulfur content beyond the typical level of 0.005 - 0.020 % S. In this way , the higher amount of sulfur increases the probability that MnS will form, and indeed survive until the moment of solidification. Thus, the presence of 0.04 % sulfur or more, in the CGI or SG base iron has been shown to result in the presence of MnS inclusions in the final cast products, thus improving their machinability.

Claims

Claims
1. A magnesium-treated cast iron such as compacted graphite cast iron (CGI) or ductile cast iron (SG) containing inclusions of mclusion-forming compounds, which either lubricate the cutting insert or contribute to the formation of a protective layer on the cutting edge.
2. A cast iron alloy according to claim 1, characterized in that the inclusions are manganese sulfids (MnS).
3. A cast iron alloy according to claim 1, characterized in that the inclusions are molybdenum disulfide (MoS2).
4. A cast iron alloy according to any of claims 1-3, characterized in that the desired inclusions are preserved by adding the magnesium alloy at the latest possible moment.
5. A cast iron alloy according to any of claims 1-3, characterized in that the desired inclusions are preserved by adding the magnesium alloy in-the-mould.
6. A cast iron alloy according to any of claims 1-3, characterized in that the desired inclusions are formed by adding a master alloy containing the inclusions at the latest possible moment.
7. A cast iron alloy according to any of claims 1-3, characterized in that the desired inclusions are formed by adding the master alloy in the mould.
8. A cast iron alloy according to any of claims 1 - 3, characterised in that the desired inclusions are formed by increasing the sulfur content to at least 0.04 % before casting.
. A cast iron product comprising an alloy according to any of claims 1-3.
10. The use of a cast iron alloy according to any of claims 1-3 to produce a cylinder block.
11. The use of a cast iron alloy according to any of claims 1-3 to produce a cylinder head.
12. The use of a cast iron alloy according to any of claims 1-3 to produce a bedplate.
13. The use of a cast iron alloy according to any of claims 1-3 to produce a transmission housing or axle housing.
14. The use of a cast iron alloy according to any of claims 1-3 to produce a brake drum or disc.
15. A method for producing a magnesium-treated cast iron containing inclusions, which either lubricate the cutting insert or contribute to the formation of a protective layer on the cutting edge, comprising the steps of: a) preparing a molten base iron according toper se known methods; b) allowing the equilibrium to form inclusions in the base iron; and c) immediately before or after casting, treating the melt with a predetermined amount of magnesium; and d) casting the melt in a per se known manner.
16. A method for producing a magnesium-treated cast iron containing inclusions, which either lubricate the cutting insert or contribute to the formation of a protective layer on the cutting edge, comprising the steps of: a) preparing a molten base iron according toper se known methods; b) adding a predetermined amount of magnesium to the molten base iron and allowing establishment of an equilibrium between magnesium, oxygen and sulfur; c) adding a predetermined amount of manganese sulfide and/or molybdenium sulfide; and finally d) casting the melt according to per se known methods.
17. A method for producing a magnesium-treated cast iron containing inclusions, which either lubricate the cutting insert or contribute to the formation of a protective layer on the cutting edge, comprising the steps of: a) preparing a molten base iron according to per se known methods, said base iron containing at least 0.1 % Mn; b) increasing the amount of sulfur to at least 0.04 %; c) adding a predetermined amount of magnesium; and d) casting the melt according toper se known methods.
18. A method according to anyone of claims 15 - 17, further comprising chilling the mould after the casting operation in order to maximise the amount of sulfide inclusions.
PCT/SE2000/002550 1999-12-17 2000-12-15 New alloy and method for producing same WO2001044530A1 (en)

Priority Applications (6)

Application Number Priority Date Filing Date Title
DE60003952T DE60003952T2 (en) 1999-12-17 2000-12-15 NEW ALLOY AND PRODUCTION METHOD THEREFOR
KR1020027007747A KR20020062761A (en) 1999-12-17 2000-12-15 New alloy and method for producing same
US10/149,653 US7081151B2 (en) 1999-12-17 2000-12-15 Alloy and method for producing same
JP2001545607A JP2003517099A (en) 1999-12-17 2000-12-15 Novel alloy and its manufacturing method
AU25639/01A AU2563901A (en) 1999-12-17 2000-12-15 New alloy and method for producing same
EP00989092A EP1252353B1 (en) 1999-12-17 2000-12-15 New alloy and method for producing same

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
SE9904668A SE9904668D0 (en) 1999-12-17 1999-12-17 New alloy and method for producing same
SE9904668-2 1999-12-17

Publications (1)

Publication Number Publication Date
WO2001044530A1 true WO2001044530A1 (en) 2001-06-21

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Country Status (8)

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EP (1) EP1252353B1 (en)
JP (1) JP2003517099A (en)
KR (1) KR20020062761A (en)
AU (1) AU2563901A (en)
DE (1) DE60003952T2 (en)
RU (1) RU2002119009A (en)
SE (1) SE9904668D0 (en)
WO (1) WO2001044530A1 (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN111676383A (en) * 2020-06-09 2020-09-18 江苏亚峰合金材料有限公司 Vermiculizer for heat-resistant cast iron and preparation method thereof

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4874576A (en) * 1988-01-23 1989-10-17 Metallgesellschaft Aktiengesellschaft Method of producing nodular cast iron
SE512201C2 (en) * 1998-03-06 2000-02-14 Sintercast Ab Process for the preparation of Mg-treated iron with improved processability

Family Cites Families (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS616250A (en) * 1984-12-10 1986-01-11 Honda Motor Co Ltd Corrosion resistant cast iron
SE8701987L (en) * 1987-05-26 1988-11-15 Fischer Ag Georg MAGNESIUM TREATED, COOLING ANGLE CAST IRON MATERIAL
GB9207139D0 (en) * 1992-04-01 1992-05-13 Brico Eng Sintered materials
JP3763603B2 (en) * 1996-01-30 2006-04-05 日本ピストンリング株式会社 Abrasion-resistant cast iron and method for producing the same
JPH108121A (en) * 1996-06-25 1998-01-13 Hitachi Metals Ltd Inoculant for producing cv graphite cast iron and production of cv graphite cast iron using the inoculant
SE520028C2 (en) * 1998-07-03 2003-05-13 Sintercast Ab Process for the preparation of compact graphite iron alloy, this article, and the use of compact graphite alloy

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4874576A (en) * 1988-01-23 1989-10-17 Metallgesellschaft Aktiengesellschaft Method of producing nodular cast iron
SE512201C2 (en) * 1998-03-06 2000-02-14 Sintercast Ab Process for the preparation of Mg-treated iron with improved processability

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN111676383A (en) * 2020-06-09 2020-09-18 江苏亚峰合金材料有限公司 Vermiculizer for heat-resistant cast iron and preparation method thereof

Also Published As

Publication number Publication date
EP1252353A1 (en) 2002-10-30
RU2002119009A (en) 2005-01-10
AU2563901A (en) 2001-06-25
SE9904668D0 (en) 1999-12-17
DE60003952T2 (en) 2004-05-27
JP2003517099A (en) 2003-05-20
KR20020062761A (en) 2002-07-29
EP1252353B1 (en) 2003-07-16
DE60003952D1 (en) 2003-08-21

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