EP0227352A2 - Metal matrix composites - Google Patents

Metal matrix composites Download PDF

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Publication number
EP0227352A2
EP0227352A2 EP86309433A EP86309433A EP0227352A2 EP 0227352 A2 EP0227352 A2 EP 0227352A2 EP 86309433 A EP86309433 A EP 86309433A EP 86309433 A EP86309433 A EP 86309433A EP 0227352 A2 EP0227352 A2 EP 0227352A2
Authority
EP
European Patent Office
Prior art keywords
bismuth
aluminium
filler material
filler
containing alloy
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.)
Ceased
Application number
EP86309433A
Other languages
German (de)
French (fr)
Other versions
EP0227352A3 (en
Inventor
Geoffrey Hugh Broomfield
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.)
UK Atomic Energy Authority
Original Assignee
UK Atomic Energy Authority
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 UK Atomic Energy Authority filed Critical UK Atomic Energy Authority
Publication of EP0227352A2 publication Critical patent/EP0227352A2/en
Publication of EP0227352A3 publication Critical patent/EP0227352A3/en
Ceased legal-status Critical Current

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Classifications

    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22CALLOYS
    • C22C1/00Making non-ferrous alloys
    • C22C1/10Alloys containing non-metals
    • C22C1/1036Alloys containing non-metals starting from a melt
    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22CALLOYS
    • C22C32/00Non-ferrous alloys containing at least 5% by weight but less than 50% by weight of oxides, carbides, borides, nitrides, silicides or other metal compounds, e.g. oxynitrides, sulfides, whether added as such or formed in situ
    • C22C32/001Non-ferrous alloys containing at least 5% by weight but less than 50% by weight of oxides, carbides, borides, nitrides, silicides or other metal compounds, e.g. oxynitrides, sulfides, whether added as such or formed in situ with only oxides
    • C22C32/0015Non-ferrous alloys containing at least 5% by weight but less than 50% by weight of oxides, carbides, borides, nitrides, silicides or other metal compounds, e.g. oxynitrides, sulfides, whether added as such or formed in situ with only oxides with only single oxides as main non-metallic constituents
    • C22C32/0036Matrix based on Al, Mg, Be or alloys thereof
    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22CALLOYS
    • C22C32/00Non-ferrous alloys containing at least 5% by weight but less than 50% by weight of oxides, carbides, borides, nitrides, silicides or other metal compounds, e.g. oxynitrides, sulfides, whether added as such or formed in situ
    • C22C32/0047Non-ferrous alloys containing at least 5% by weight but less than 50% by weight of oxides, carbides, borides, nitrides, silicides or other metal compounds, e.g. oxynitrides, sulfides, whether added as such or formed in situ with carbides, nitrides, borides or silicides as the main non-metallic constituents
    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22CALLOYS
    • C22C32/00Non-ferrous alloys containing at least 5% by weight but less than 50% by weight of oxides, carbides, borides, nitrides, silicides or other metal compounds, e.g. oxynitrides, sulfides, whether added as such or formed in situ
    • C22C32/0089Non-ferrous alloys containing at least 5% by weight but less than 50% by weight of oxides, carbides, borides, nitrides, silicides or other metal compounds, e.g. oxynitrides, sulfides, whether added as such or formed in situ with other, not previously mentioned inorganic compounds as the main non-metallic constituent, e.g. sulfides, glass

Definitions

  • This invention relates to a method of making metal matrix composites where the metal is aluminium or an alloy thereof.
  • Metal matrix composites comprising a refractory inorganic filler material such as silicon carbide or alumina in a matrix of aluminium or an alloy thereof are useful engineering materials, for example where high strength and low density are required as in the motor vehicle and aerospace industries.
  • molten Al or Al alloy cannot wet the solid filler material sufficiently for such composites to be made satisfactorily by stirring the filler into the molten metal.
  • the invention provides a method of making a solid composite material comprising a refractory, inorganic filler material in a matrix of aluminium or an aluminium-containing alloy such as an aluminium base alloy, which comprises
  • the molten Al or alloy takes up at least twice the amount of filler by weight when the bismuth additive is present than when it is absent, and further that the filler is more uniformly dispersed in the matrix when a bismuth additive is used.
  • the filler material may be a material known in the art for enhancing the properties of aluminium and aluminium base alloys.
  • examples are refractory carbides such as silicon carbide and refractory oxides such as alumina.
  • the bismuth additive is a bismuth compound such as bismuth oxide when the dispersion may be prepared in step (i) by intimately mixing fine particle elemental bismuth with particulate filler material, for example of particle size in the range of 5 ⁇ m to 100 ⁇ m wherein the weight of bismuth is preferably less than 10% of the weight of the filler, followed by oxidising the elemental bismuth to bismuth oxide (Bi2O3), e.g. by heating in air at 500°C to 1000°C. Heating in air causes the bismuth to burn and generate smoke thereby facilitating production of a fine oxide dispersion.
  • oxidising the elemental bismuth to bismuth oxide e.g. by heating in air at 500°C to 1000°C. Heating in air causes the bismuth to burn and generate smoke thereby facilitating production of a fine oxide dispersion.
  • step (i) it may however be possible to prepare the dispersion in step (i) in other ways, for example by mixing the filler material with an aqueous solution of a decomposable bismuth salt such as bismuth nitrate followed by heating to decompose the salt to bismuth oxide.
  • a decomposable bismuth salt such as bismuth nitrate
  • Step (ii) may be carried out by the known technique of vacuum stirring wherein the dispersion of step (i) is stirred into the molten aluminium or aluminium base alloy in vacuo.
  • the aluminium or aluminium base alloy may be at a temperature considerably above its liquidus, for example at 150°C above its liquidus.
  • bismuth compounds embrittle aluminium and aluminium base alloys at elevated temperature. It may, therefore, be necessary to add a material capable of reacting with surplus bismuth additive, i.e. a bismuth "getter", between steps (ii) and (iii). Examples of such getters are magnesium and manganese.
  • a bismuth getter may not be necessary in all cases; for example, an aluminium base alloy, if used, may contain a getter as a component thereof and hence provide at sufficient quantity of the getter.
  • the composite material produced in step (iii) may, for example, be pressure die cast, squeeze cast, chill cast or wrought.
  • a shaped composite may be produced directly in step (iii) by cooling the product of step (ii) in a mould.
  • the composite produced by this invention may have a range of compositions subject to product and/or processing requirements and restrictions.
  • Step (ii) The above dispersion was stirred into an aluminium base alloy (LM6, containing ⁇ 10.5% Si) in vacuo for 2 hours in the temperature range of 740°C to 770°C.
  • LM6 aluminium base alloy
  • Step (iii) The molten product of step (ii) was cooled to the freezing point of the alloy in about half an hour.
  • the alloy had taken up about 20% of its weight of alumina which was fairly uniformly distributed therein on a macro scale.
  • the material was capable of being melted and chill cast and pressure die cast without undue difficulty.
  • a sample of the material was heated to 850°C and poured through a 10 mm hole under a head of approximately 20 mm to show that it was sufficiently fluid when molten to be cast.
  • the material was then heated to 850°C and cast into a cast iron mould. Sections of the resulting casting were examined microscopically where it was observed that the alumina filler material had been retained and that its distribution in the matrix was, if anything, more uniform than in the composite material product of step (iii).

Abstract

A composite material comprising a refractory, inorganic filler material (e.g. SiC or Al₂O₃) in a matrix of aluminium or an aluminium-containing alloy is made by incorporating the filler material into the aluminium or aluminium-containing alloy at a temperature above its liquidus, e.g. by vacuum stirring, followed by cooling to solidify the composite. In order to improve the wettability of the filler by the molten metal, the filler has a bismuth additive, for example in the form of a bismuth compound such as bismuth oxide, dispersed therein. This may be done by intimately mixing elemental bismuth with particulate filler followed by oxidation of the bismuth to bismuth oxide. e.g. by heating in air.

Description

  • This invention relates to a method of making metal matrix composites where the metal is aluminium or an alloy thereof.
  • Metal matrix composites comprising a refractory inorganic filler material such as silicon carbide or alumina in a matrix of aluminium or an alloy thereof are useful engineering materials, for example where high strength and low density are required as in the motor vehicle and aerospace industries. However, molten Al or Al alloy cannot wet the solid filler material sufficiently for such composites to be made satisfactorily by stirring the filler into the molten metal.
  • It has now been found that this problem may be ameliorated by using a particular additive with the filler. Thus, the invention provides a method of making a solid composite material comprising a refractory, inorganic filler material in a matrix of aluminium or an aluminium-containing alloy such as an aluminium base alloy, which comprises
    • (i) preparing a uniform dispersion of a bismuth additive in the filler material;
    • (ii) incorporating the dispersion into the aluminium or aluminium-containing alloy, the aluminium or aluminium-­containing alloy being at a temperature above its liquidus; and
    • (iii) cooling the product of step (ii) to produce a solid composite material.
  • It has been found, in specific examples of this method, that the molten Al or alloy takes up at least twice the amount of filler by weight when the bismuth additive is present than when it is absent, and further that the filler is more uniformly dispersed in the matrix when a bismuth additive is used.
  • The filler material may be a material known in the art for enhancing the properties of aluminium and aluminium base alloys. Examples are refractory carbides such as silicon carbide and refractory oxides such as alumina.
  • Preferably the bismuth additive is a bismuth compound such as bismuth oxide when the dispersion may be prepared in step (i) by intimately mixing fine particle elemental bismuth with particulate filler material, for example of particle size in the range of 5 µm to 100 µm wherein the weight of bismuth is preferably less than 10% of the weight of the filler, followed by oxidising the elemental bismuth to bismuth oxide (Bi₂O₃), e.g. by heating in air at 500°C to 1000°C. Heating in air causes the bismuth to burn and generate smoke thereby facilitating production of a fine oxide dispersion.
  • It may however be possible to prepare the dispersion in step (i) in other ways, for example by mixing the filler material with an aqueous solution of a decomposable bismuth salt such as bismuth nitrate followed by heating to decompose the salt to bismuth oxide.
  • Step (ii) may be carried out by the known technique of vacuum stirring wherein the dispersion of step (i) is stirred into the molten aluminium or aluminium base alloy in vacuo. The aluminium or aluminium base alloy may be at a temperature considerably above its liquidus, for example at 150°C above its liquidus.
  • The presence of bismuth compounds is known to embrittle aluminium and aluminium base alloys at elevated temperature. It may, therefore, be necessary to add a material capable of reacting with surplus bismuth additive, i.e. a bismuth "getter", between steps (ii) and (iii). Examples of such getters are magnesium and manganese. However, a bismuth getter may not be necessary in all cases; for example, an aluminium base alloy, if used, may contain a getter as a component thereof and hence provide at sufficient quantity of the getter.
  • To produce a finished shaped article, the composite material produced in step (iii) may, for example, be pressure die cast, squeeze cast, chill cast or wrought. However, a shaped composite may be produced directly in step (iii) by cooling the product of step (ii) in a mould.
  • The composite produced by this invention may have a range of compositions subject to product and/or processing requirements and restrictions.
  • The following example illustrates the invention.
  • EXAMPLE
  • Step (i) Elemental bismuth in the form of fine filings was added to fused and crushed alumina (approximately 9 µm particle size), wherein the weight of bismuth was 2% of that of the alumina, and thoroughly mixed by barrelling. The resulting mixture was then heated in air at 550°C for 2 hours to oxidise the bismuth to bismuth oxide thereby producing a uniform dispersion of bismuth oxide in alumina.
  • Step (ii) The above dispersion was stirred into an aluminium base alloy (LM6, containing ≃ 10.5% Si) in vacuo for 2 hours in the temperature range of 740°C to 770°C.
  • Step (iii) The molten product of step (ii) was cooled to the freezing point of the alloy in about half an hour.
  • In the resulting material, the alloy had taken up about 20% of its weight of alumina which was fairly uniformly distributed therein on a macro scale. The material was capable of being melted and chill cast and pressure die cast without undue difficulty. In particular, a sample of the material was heated to 850°C and poured through a 10 mm hole under a head of approximately 20 mm to show that it was sufficiently fluid when molten to be cast. The material was then heated to 850°C and cast into a cast iron mould. Sections of the resulting casting were examined microscopically where it was observed that the alumina filler material had been retained and that its distribution in the matrix was, if anything, more uniform than in the composite material product of step (iii).
  • The above result was considerably superior to any of those obtained in 19 experiments in which the above process steps were repeated but in the absence of a bismuth additive.

Claims (10)

1. A method of making a solid composite material comprising a refractory, inorganic filler material in a matrix of aluminium or an aluminium-containing alloy, which comprises
(a) incorporating the filler material into the aluminium or aluminium-containing alloy, the aluminium or aluminium-­containing alloy being at a temperature above its liquidus; and
(b) cooling the product of step (a) to produce a solid composite material,
characterised in that the filler material has a bismuth additive uniformly dispersed therein.
2. A method according to claim 1 wherein the bismuth additive is bismuth oxide.
3. A method according to claim 2 wherein the bismuth oxide is dispersed in the filler material by intimately mixing elemental bismuth therewith, followed by oxidising the elemental bismuth to bismuth oxide.
4. A method according to claim 3 wherein the bismuth is oxidised by heating it in air.
5. A method according to claim 4 wherein the temperature of the heating is in the range of 500°C to 1000°C.
6. A method according to any of the preceding claims wherein the filler material has a particle size in the range of 5 µm to 100 µm.
7. A method according to any of the preceding claims wherein step (a) comprises vacuum stirring.
8. A method according to any of the preceding claims wherein the filler material is silicon carbide or alumina.
9. A method according to any of the preceding claims wherein the solid composite material is melted and cast to give a shaped article.
10. A method according to any of the preceding claims wherein the matrix is of an aluminium-base alloy.
EP86309433A 1985-12-17 1986-12-03 Metal matrix composites Ceased EP0227352A3 (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
GB858531070A GB8531070D0 (en) 1985-12-17 1985-12-17 Metal matrix composites
GB8531070 1985-12-17

Publications (2)

Publication Number Publication Date
EP0227352A2 true EP0227352A2 (en) 1987-07-01
EP0227352A3 EP0227352A3 (en) 1989-03-08

Family

ID=10589894

Family Applications (1)

Application Number Title Priority Date Filing Date
EP86309433A Ceased EP0227352A3 (en) 1985-12-17 1986-12-03 Metal matrix composites

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EP (1) EP0227352A3 (en)
JP (1) JPS62146229A (en)
GB (2) GB8531070D0 (en)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH072980B2 (en) * 1990-09-20 1995-01-18 大同メタル工業株式会社 Composite sliding material
GB9302921D0 (en) * 1993-02-13 1993-03-31 Atomic Energy Authority Uk Particulate metal matrix composites

Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE1111836B (en) * 1957-07-05 1961-07-27 Gen Electric Co Ltd Process for the preparation of a suspension of thorium oxide in the melt of a low-melting metal or such an alloy and application to nuclear reactors
FR1276929A (en) * 1960-12-28 1961-11-24 Bendix Corp Improvements to friction materials
GB959442A (en) * 1960-06-13 1964-06-03 Du Pont Improvements in or relating to metalliferous compositions
US4189522A (en) * 1975-08-08 1980-02-19 Daido Metal Company, Ltd. Multi-layer sliding material and method for manufacturing the same

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE1111836B (en) * 1957-07-05 1961-07-27 Gen Electric Co Ltd Process for the preparation of a suspension of thorium oxide in the melt of a low-melting metal or such an alloy and application to nuclear reactors
GB959442A (en) * 1960-06-13 1964-06-03 Du Pont Improvements in or relating to metalliferous compositions
FR1276929A (en) * 1960-12-28 1961-11-24 Bendix Corp Improvements to friction materials
US4189522A (en) * 1975-08-08 1980-02-19 Daido Metal Company, Ltd. Multi-layer sliding material and method for manufacturing the same

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
PATENT ABSTRACTS OF JAPAN, vol. 10, no. 123 (C-344)[2180], 8th May 1986; & JP-A-60 251 150 (OKUNO SEIYAKU KOGYO K.K.) 11-12-1985 *

Also Published As

Publication number Publication date
GB2184133A (en) 1987-06-17
JPS62146229A (en) 1987-06-30
GB8531070D0 (en) 1986-01-29
EP0227352A3 (en) 1989-03-08
GB2184133B (en) 1989-07-12
GB8628885D0 (en) 1987-01-07

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Inventor name: BROOMFIELD, GEOFFREY HUGH