CA2232177A1 - Aluminium matrix composite material and process of producing same - Google Patents
Aluminium matrix composite material and process of producing same Download PDFInfo
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- CA2232177A1 CA2232177A1 CA002232177A CA2232177A CA2232177A1 CA 2232177 A1 CA2232177 A1 CA 2232177A1 CA 002232177 A CA002232177 A CA 002232177A CA 2232177 A CA2232177 A CA 2232177A CA 2232177 A1 CA2232177 A1 CA 2232177A1
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- Prior art keywords
- aluminium
- fibre
- preform
- composite material
- matrix composite
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- 239000002131 composite material Substances 0.000 title claims abstract description 51
- 239000011159 matrix material Substances 0.000 title claims abstract description 49
- 239000004411 aluminium Substances 0.000 title claims abstract description 42
- 229910052782 aluminium Inorganic materials 0.000 title claims abstract description 42
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 title claims abstract description 42
- 238000000034 method Methods 0.000 title claims abstract description 25
- 230000008569 process Effects 0.000 title claims abstract description 24
- 239000000835 fiber Substances 0.000 claims abstract description 52
- 229910000838 Al alloy Inorganic materials 0.000 claims abstract description 16
- 239000000155 melt Substances 0.000 claims abstract description 6
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 claims abstract description 5
- 229910052710 silicon Inorganic materials 0.000 claims abstract description 5
- 239000010703 silicon Substances 0.000 claims abstract description 5
- 239000000463 material Substances 0.000 claims description 29
- 229910045601 alloy Inorganic materials 0.000 claims description 9
- 239000000956 alloy Substances 0.000 claims description 9
- 230000008595 infiltration Effects 0.000 claims description 8
- 238000001764 infiltration Methods 0.000 claims description 8
- 229910052751 metal Inorganic materials 0.000 claims description 7
- 239000002184 metal Substances 0.000 claims description 7
- 239000011148 porous material Substances 0.000 claims description 7
- 238000005266 casting Methods 0.000 claims description 5
- 238000004512 die casting Methods 0.000 claims description 5
- XEEYBQQBJWHFJM-UHFFFAOYSA-N iron Substances [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 claims description 5
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 claims description 4
- YPFNIPKMNMDDDB-UHFFFAOYSA-K 2-[2-[bis(carboxylatomethyl)amino]ethyl-(2-hydroxyethyl)amino]acetate;iron(3+) Chemical compound [Fe+3].OCCN(CC([O-])=O)CCN(CC([O-])=O)CC([O-])=O YPFNIPKMNMDDDB-UHFFFAOYSA-K 0.000 claims description 2
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 claims description 2
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 claims description 2
- 239000010941 cobalt Substances 0.000 claims description 2
- 229910017052 cobalt Inorganic materials 0.000 claims description 2
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 claims description 2
- 229910052802 copper Inorganic materials 0.000 claims description 2
- 239000010949 copper Substances 0.000 claims description 2
- 229910000765 intermetallic Inorganic materials 0.000 claims description 2
- 229910052749 magnesium Inorganic materials 0.000 claims description 2
- 239000011777 magnesium Substances 0.000 claims description 2
- 230000003647 oxidation Effects 0.000 claims description 2
- 238000007254 oxidation reaction Methods 0.000 claims description 2
- 229910021324 titanium aluminide Inorganic materials 0.000 claims description 2
- WFKWXMTUELFFGS-UHFFFAOYSA-N tungsten Chemical compound [W] WFKWXMTUELFFGS-UHFFFAOYSA-N 0.000 claims description 2
- 229910052721 tungsten Inorganic materials 0.000 claims description 2
- 239000010937 tungsten Substances 0.000 claims description 2
- 239000000274 aluminium melt Substances 0.000 claims 2
- 238000000605 extraction Methods 0.000 claims 2
- 229910001151 AlNi Inorganic materials 0.000 claims 1
- 229910017150 AlTi Inorganic materials 0.000 claims 1
- 229910000951 Aluminide Inorganic materials 0.000 claims 1
- 229920000914 Metallic fiber Polymers 0.000 claims 1
- 229910000990 Ni alloy Inorganic materials 0.000 claims 1
- 229910000545 Nickel–aluminium alloy Inorganic materials 0.000 claims 1
- NPXOKRUENSOPAO-UHFFFAOYSA-N Raney nickel Chemical compound [Al].[Ni] NPXOKRUENSOPAO-UHFFFAOYSA-N 0.000 claims 1
- -1 aluminium silicon magnesium zinc Chemical compound 0.000 claims 1
- 239000011651 chromium Substances 0.000 claims 1
- UPHIPHFJVNKLMR-UHFFFAOYSA-N chromium iron Chemical compound [Cr].[Fe] UPHIPHFJVNKLMR-UHFFFAOYSA-N 0.000 claims 1
- 238000009792 diffusion process Methods 0.000 claims 1
- 230000005484 gravity Effects 0.000 claims 1
- UGKDIUIOSMUOAW-UHFFFAOYSA-N iron nickel Chemical compound [Fe].[Ni] UGKDIUIOSMUOAW-UHFFFAOYSA-N 0.000 claims 1
- 150000002739 metals Chemical class 0.000 claims 1
- 230000000704 physical effect Effects 0.000 claims 1
- 238000005245 sintering Methods 0.000 claims 1
- 239000000126 substance Substances 0.000 claims 1
- 239000000919 ceramic Substances 0.000 description 8
- 238000009736 wetting Methods 0.000 description 6
- 238000003754 machining Methods 0.000 description 4
- 238000004519 manufacturing process Methods 0.000 description 4
- 239000000203 mixture Substances 0.000 description 3
- 239000003921 oil Substances 0.000 description 3
- 230000015572 biosynthetic process Effects 0.000 description 2
- 238000002485 combustion reaction Methods 0.000 description 2
- 230000001419 dependent effect Effects 0.000 description 2
- 229910052742 iron Inorganic materials 0.000 description 2
- 239000007769 metal material Substances 0.000 description 2
- 230000000630 rising effect Effects 0.000 description 2
- 229910000831 Steel Inorganic materials 0.000 description 1
- 238000005299 abrasion Methods 0.000 description 1
- 230000001133 acceleration Effects 0.000 description 1
- 238000004873 anchoring Methods 0.000 description 1
- 238000007664 blowing Methods 0.000 description 1
- JEZHBSJTXKKFMV-UHFFFAOYSA-N calcium nickel Chemical compound [Ca].[Ni] JEZHBSJTXKKFMV-UHFFFAOYSA-N 0.000 description 1
- 229910052918 calcium silicate Inorganic materials 0.000 description 1
- 239000000378 calcium silicate Substances 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 230000007797 corrosion Effects 0.000 description 1
- 238000005260 corrosion Methods 0.000 description 1
- 238000009826 distribution Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000002347 injection Methods 0.000 description 1
- 239000007924 injection Substances 0.000 description 1
- 150000001247 metal acetylides Chemical class 0.000 description 1
- 229910052759 nickel Inorganic materials 0.000 description 1
- 150000004767 nitrides Chemical class 0.000 description 1
- 239000011224 oxide ceramic Substances 0.000 description 1
- 229910052574 oxide ceramic Inorganic materials 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 238000004064 recycling Methods 0.000 description 1
- 230000003014 reinforcing effect Effects 0.000 description 1
- 238000007789 sealing Methods 0.000 description 1
- 230000035939 shock Effects 0.000 description 1
- 238000007711 solidification Methods 0.000 description 1
- 230000008023 solidification Effects 0.000 description 1
- 238000001228 spectrum Methods 0.000 description 1
- 239000010959 steel Substances 0.000 description 1
- 230000003746 surface roughness Effects 0.000 description 1
- 230000007704 transition Effects 0.000 description 1
- 230000000007 visual effect Effects 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C47/00—Making alloys containing metallic or non-metallic fibres or filaments
- C22C47/02—Pretreatment of the fibres or filaments
- C22C47/025—Aligning or orienting the fibres
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B22—CASTING; POWDER METALLURGY
- B22D—CASTING OF METALS; CASTING OF OTHER SUBSTANCES BY THE SAME PROCESSES OR DEVICES
- B22D19/00—Casting in, on, or around objects which form part of the product
- B22D19/14—Casting in, on, or around objects which form part of the product the objects being filamentary or particulate in form
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B22—CASTING; POWDER METALLURGY
- B22F—WORKING METALLIC POWDER; MANUFACTURE OF ARTICLES FROM METALLIC POWDER; MAKING METALLIC POWDER; APPARATUS OR DEVICES SPECIALLY ADAPTED FOR METALLIC POWDER
- B22F1/00—Metallic powder; Treatment of metallic powder, e.g. to facilitate working or to improve properties
- B22F1/06—Metallic powder characterised by the shape of the particles
- B22F1/062—Fibrous particles
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B15/00—Layered products comprising a layer of metal
- B32B15/14—Layered products comprising a layer of metal next to a fibrous or filamentary layer
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B5/00—Layered products characterised by the non- homogeneity or physical structure, i.e. comprising a fibrous, filamentary, particulate or foam layer; Layered products characterised by having a layer differing constitutionally or physically in different parts
- B32B5/14—Layered products characterised by the non- homogeneity or physical structure, i.e. comprising a fibrous, filamentary, particulate or foam layer; Layered products characterised by having a layer differing constitutionally or physically in different parts characterised by a layer differing constitutionally or physically in different parts, e.g. denser near its faces
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B5/00—Layered products characterised by the non- homogeneity or physical structure, i.e. comprising a fibrous, filamentary, particulate or foam layer; Layered products characterised by having a layer differing constitutionally or physically in different parts
- B32B5/22—Layered products characterised by the non- homogeneity or physical structure, i.e. comprising a fibrous, filamentary, particulate or foam layer; Layered products characterised by having a layer differing constitutionally or physically in different parts characterised by the presence of two or more layers which are next to each other and are fibrous, filamentary, formed of particles or foamed
- B32B5/24—Layered products characterised by the non- homogeneity or physical structure, i.e. comprising a fibrous, filamentary, particulate or foam layer; Layered products characterised by having a layer differing constitutionally or physically in different parts characterised by the presence of two or more layers which are next to each other and are fibrous, filamentary, formed of particles or foamed one layer being a fibrous or filamentary layer
- B32B5/26—Layered products characterised by the non- homogeneity or physical structure, i.e. comprising a fibrous, filamentary, particulate or foam layer; Layered products characterised by having a layer differing constitutionally or physically in different parts characterised by the presence of two or more layers which are next to each other and are fibrous, filamentary, formed of particles or foamed one layer being a fibrous or filamentary layer another layer next to it also being fibrous or filamentary
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C47/00—Making alloys containing metallic or non-metallic fibres or filaments
- C22C47/02—Pretreatment of the fibres or filaments
- C22C47/06—Pretreatment of the fibres or filaments by forming the fibres or filaments into a preformed structure, e.g. using a temporary binder to form a mat-like element
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C47/00—Making alloys containing metallic or non-metallic fibres or filaments
- C22C47/08—Making alloys containing metallic or non-metallic fibres or filaments by contacting the fibres or filaments with molten metal, e.g. by infiltrating the fibres or filaments placed in a mould
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C49/00—Alloys containing metallic or non-metallic fibres or filaments
- C22C49/02—Alloys containing metallic or non-metallic fibres or filaments characterised by the matrix material
- C22C49/04—Light metals
-
- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F02—COMBUSTION ENGINES; HOT-GAS OR COMBUSTION-PRODUCT ENGINE PLANTS
- F02F—CYLINDERS, PISTONS OR CASINGS, FOR COMBUSTION ENGINES; ARRANGEMENTS OF SEALINGS IN COMBUSTION ENGINES
- F02F7/00—Casings, e.g. crankcases or frames
- F02F7/0085—Materials for constructing engines or their parts
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B22—CASTING; POWDER METALLURGY
- B22F—WORKING METALLIC POWDER; MANUFACTURE OF ARTICLES FROM METALLIC POWDER; MAKING METALLIC POWDER; APPARATUS OR DEVICES SPECIALLY ADAPTED FOR METALLIC POWDER
- B22F2998/00—Supplementary information concerning processes or compositions relating to powder metallurgy
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B22—CASTING; POWDER METALLURGY
- B22F—WORKING METALLIC POWDER; MANUFACTURE OF ARTICLES FROM METALLIC POWDER; MAKING METALLIC POWDER; APPARATUS OR DEVICES SPECIALLY ADAPTED FOR METALLIC POWDER
- B22F2999/00—Aspects linked to processes or compositions used in powder metallurgy
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C2204/00—End product comprising different layers, coatings or parts of cermet
-
- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F05—INDEXING SCHEMES RELATING TO ENGINES OR PUMPS IN VARIOUS SUBCLASSES OF CLASSES F01-F04
- F05C—INDEXING SCHEME RELATING TO MATERIALS, MATERIAL PROPERTIES OR MATERIAL CHARACTERISTICS FOR MACHINES, ENGINES OR PUMPS OTHER THAN NON-POSITIVE-DISPLACEMENT MACHINES OR ENGINES
- F05C2253/00—Other material characteristics; Treatment of material
- F05C2253/16—Fibres
Landscapes
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Mechanical Engineering (AREA)
- Materials Engineering (AREA)
- Metallurgy (AREA)
- Organic Chemistry (AREA)
- Nanotechnology (AREA)
- Combustion & Propulsion (AREA)
- General Engineering & Computer Science (AREA)
- Crystallography & Structural Chemistry (AREA)
- Manufacture Of Alloys Or Alloy Compounds (AREA)
- Forging (AREA)
- Powder Metallurgy (AREA)
- Chemical Or Physical Treatment Of Fibers (AREA)
- Laminated Bodies (AREA)
Abstract
The invention relates to an aluminium matrix composite material consisting of a porous fibre preform which is embedded in an aluminium alloy and which has a higher strength and an improved wear behaviour as compared to the aluminium matrix, wherein the fibre preform consists of a shaped fibre member which comprises a metallic and/or intermetallic structure and into which there is infiltrated a silicon-containing aluminium alloy melt, with the Si-content of the melt amounting to 5 - 14 % by weight. Furthermore, the invention relates to a process of producing an aluminium matrix composite material which consists of a porous fibre preform infiltrated with an aluminium alloy.
Description
VAN motor GmbH 28th January 1998 Friedrich-Wohler-Str. 2 MW/scb (allO771) 53117 Bonn P96906EO10 Aluminium matrix composite material and process of producing same Description The invention relates to an aluminium matrix composite material consisting of a porous fibre preform which is embedded in an aluminium alloy and which has a higher strength and an improved wear behaviour as compared to the aluminium matrix, and to a process of producing such composite materials.
Such aluminium matrix composite materials are produced for example in the form of single cylinder blocks or multi-cylinder blocks from an aluminium alloy, and into the cylinder there is cast a hollow-cylindrical member consisting of ceramic fibres with silicon members inserted into same, which hollow-cylindrical member forms the cylinder barrel and is penetrated by a hypoeutectic aluminium alloy. The purpose of this measure is to improve the tribological properties of the cylinder barrel face.
One problem which occurs when subjecting such composite materials to mechanical loads consists in that the high silicon content results in an increase in tool wear when machining the cylinder block and causes piston wear under operational conditions. Said disadvantage can be reduced in that the proportion of fibres and the percentage of sicilon grains are calculated to be such that a large area of contact between the aluminium alloy matrix of the cylinder and the tool and piston respectively is avoided. Nevertheless, the piston shank has to be provided with a layer of iron in order to keep the piston shank wear within acceptable limits.
A further problem of the prior art fibre composite materials consists in that the raw materials can only be re-used if they are subjected to expensive recycling processes which include additional separating stages for the fibres. Such processes are not able to separate metallic and non-metallic materials completely which, therefore, subsequently, have to be processed separately.
Furthermore, the wetting behaviour of ceramic fibres when coming into contact with metal melts is known to be very disadvantageous. Therefore, it has so far been regarded as necessary to allow the aluminium alloy melt to act under high pressures of up to 3000 bar up to the point of solidification. This greatly increases the costs of producing aluminium matrix composite materials.
The same applies to reinforcing elements which are produced from spray-compacted materials and which, in accordance with EP O 271 222 A2, may consist of several layers of fireproof materials. However, in this case there is a risk of a reaction between the fibre material and the melt, so that infiltration times have to be kept short to prevent the formation of metal carbides or metal nitrides.
Furthermore, following a large number of tests it has been found that, as a result of the different temperature behaviour of ceramics and metal materials, there may occur very disadvantageous tolerance ranges under the different operating conditions of internal combustion engines. Under extreme conditions, these differences lead to the formation of grooves between the piston shank and the cylinder barrel or, in another extreme case, to increased oil losses due to through-blowing effects.
It is the object of the present invention to improve the tribological properties of prior art aluminium matrix composite materials, especially when used for cylinder sleeves for engine blocks and to narrow the tolerance range by adapting the temperature-dependent material properties to one another, with the disadvantages of prior art aluminium matrix composite materials being avoided by improving the wetting behaviour during infiltration.
This objective is achieved by the characteristics listed in the claims.
The wear behaviour of an aluminium matrix composite material produced in accordance with the invention can be influenced as follows:
1. For the first time, it has become possible to produce pairs of the same type of (metallic) material for the friction partners of fibre-reinforced materials, with the temperature-dependent strength behaviour of same being improved considerably.
Such aluminium matrix composite materials are produced for example in the form of single cylinder blocks or multi-cylinder blocks from an aluminium alloy, and into the cylinder there is cast a hollow-cylindrical member consisting of ceramic fibres with silicon members inserted into same, which hollow-cylindrical member forms the cylinder barrel and is penetrated by a hypoeutectic aluminium alloy. The purpose of this measure is to improve the tribological properties of the cylinder barrel face.
One problem which occurs when subjecting such composite materials to mechanical loads consists in that the high silicon content results in an increase in tool wear when machining the cylinder block and causes piston wear under operational conditions. Said disadvantage can be reduced in that the proportion of fibres and the percentage of sicilon grains are calculated to be such that a large area of contact between the aluminium alloy matrix of the cylinder and the tool and piston respectively is avoided. Nevertheless, the piston shank has to be provided with a layer of iron in order to keep the piston shank wear within acceptable limits.
A further problem of the prior art fibre composite materials consists in that the raw materials can only be re-used if they are subjected to expensive recycling processes which include additional separating stages for the fibres. Such processes are not able to separate metallic and non-metallic materials completely which, therefore, subsequently, have to be processed separately.
Furthermore, the wetting behaviour of ceramic fibres when coming into contact with metal melts is known to be very disadvantageous. Therefore, it has so far been regarded as necessary to allow the aluminium alloy melt to act under high pressures of up to 3000 bar up to the point of solidification. This greatly increases the costs of producing aluminium matrix composite materials.
The same applies to reinforcing elements which are produced from spray-compacted materials and which, in accordance with EP O 271 222 A2, may consist of several layers of fireproof materials. However, in this case there is a risk of a reaction between the fibre material and the melt, so that infiltration times have to be kept short to prevent the formation of metal carbides or metal nitrides.
Furthermore, following a large number of tests it has been found that, as a result of the different temperature behaviour of ceramics and metal materials, there may occur very disadvantageous tolerance ranges under the different operating conditions of internal combustion engines. Under extreme conditions, these differences lead to the formation of grooves between the piston shank and the cylinder barrel or, in another extreme case, to increased oil losses due to through-blowing effects.
It is the object of the present invention to improve the tribological properties of prior art aluminium matrix composite materials, especially when used for cylinder sleeves for engine blocks and to narrow the tolerance range by adapting the temperature-dependent material properties to one another, with the disadvantages of prior art aluminium matrix composite materials being avoided by improving the wetting behaviour during infiltration.
This objective is achieved by the characteristics listed in the claims.
The wear behaviour of an aluminium matrix composite material produced in accordance with the invention can be influenced as follows:
1. For the first time, it has become possible to produce pairs of the same type of (metallic) material for the friction partners of fibre-reinforced materials, with the temperature-dependent strength behaviour of same being improved considerably.
2. By controlling the pore size it is possible to influence the distribution of volume of the matrix and of the fibre content, so that the stength values and friction pairs can be set locally.
3. In an extreme case, the friction faces can be produced entirely from fibre materials and the visual faces can be produced entirely from a metal matrix.
The extreme case referred to above can be explained with the help of the following example:
When used for the cylinder barrels of a single- or multi-cylinder engine, the inventive aluminium matrix composite material can be provided with particularly advantageous properties when tolerances and clearances have to be compensated for. By using the same type of material (infiltration material) for cylinder sleeve faces and outer piston faces, no dimensional deviations between the used materials have been identified, neither when cold-starting an engine nor under continuous operating conditions, neither during acceleration cycles nor full throttle cycles. This means that also the emission behaviour of the inventive running faces of single- or multi-cylinder engines has been improved considerably over the entire operational range, as compared to conventionally produced composite materials reinforced by fully ceramic fibres.
A further advantage refers to the advantageous wetting behaviour during infiltration because the metallic and/or intermetallic fibres can be wetted particularly easily by an aluminium casting alloy, i.e. also in a pressure-less way. This is particularly important in connection with automated processes, for example in the case of pressure die casting processes, because the individual process stages can take place in a relatively short time while nevertheless ensuring complete wetting of the fibres of the fibre preform. Satisfactory wetting means that the die is well filled and that the fibre preform is well anchored in the matrix, so that the dimensional stability of the composite material in accordance with the invention is at least twice as high as that of a conventionally die-cast aluminium matrix material with oxide-ceramic fibres.
As a result of the improved dimensional stability of the fibre preform it is also possible to achieve high production speeds when using modern production processs.
For instance, it is possible to speed up the injecting sequence while simultaneously increasing the injection pressure during the pressure die casting process, so that, while the number of rejects is reduced, the production output is more than three times as high as that of comparable composite materials based on ceramics.
The proportion of fibres of the inventive aluminium matrix composite material can be adapted to the loads applied in the respective application. It is thus possible to produce new composite materials with a gradient structure and specific strength/elongation properties. Production costs are thus reduced, especially in the case of components with complicated shapes.
Comprehensive machining operations on the working surface with the improved rheological properties can be avoided if the part is designed accordingly. The process in accordance with the invention makes it possible to provide a component with both highly loaded sliding faces and temperature-loaded sealing faces, e.g. in the cylinder head region. Even tensioned parts with an improved elongation behaviour can be produced by a cost-effective overall process.
Decisive factors in this context are the structure, design and composition of the fibre preform which may comprise anopen-pore metallic structure in the porosity range of 30 - 97% with pore sizes of 1 ~ to 3 mm.
Furthermore, the surface roughness of the porous structure can be varied, which means that the ability of the melt to infiltrate the porous structure can be influenced. It is thus possible to achieve very good mechanical anchoring of the fibres with the help of a rough structure, whereas with a smooth fibre surface, the porous structure can be infiltrated more easily.
As the inventive aluminium matrix composite material consists of constituents of the same type, it has a homogeneous strength structure which results in a very good thermal shock behaviour, and since, furthermore, because of its metallic basis, its thermal conductivity reaches very high values, it is particularly suitable for being used in internal combustion engines. In addition, it is very suitable for chip-forming and non-chip-forming machining operations, especially in the transition zone between purely metallic and aluminium matrix composite materials, which so far led to problems due to different material structures.
To be able to use cylinder barrels made of composite materials it is necessary for the expansion coefficient of the shaped fibre members to be largely adapted to the matrix material and the base alloy. This has been achieved for the first time with the aluminium matrix composite material in accordance with the invention because the shaped fibre member consisting of a metallic and/or intermetallic fibre material can be largely adapted to its metallic environment by changing its composition. Porous ceramic structures, on the other hand, have a very limited spectrum of properties.
For optimising the wear properties, there are available the base materials of iron and nickel or the intermetallics such as iron-, nickel-, titanium-aluminides, tungsten, copper, cobalt, magnesium. Depending on requirements, it is possible, by selecting a suitable combination, advantageously to combine specific properties such as low density, good thermal conductivity, good corrosion resistance and good machining properties.
In addition to selecting the material, it is possible in the case of the aluminium matrix composite material, to achieve a gradient structure in the fibre preform.
For example, said member may comprise a rising or falling porosity or a rising or falling pore size across its cross-section. In this way it is possible to ensure that the properties of the metal matrix fibre composite meet the load requirements.
Below, there will be described an example of producing the inventive aluminium matrix composite material and some specific preferred applications which demonstrate the inventive idea and reveal further advantageous properties. In particular, reference is made to using the above material as a bearing material according to Figure 2, for a cylinder barrel according to Figure 3, and for a valve seat according to Figure 4.
As can be seen in Figure 1, process stage I, first a shaped fibre member 9 is connected, and provided with a firm structure, by being sintered in a furnace 10.
After the shaped fibre member has cooled down, it can be converted into a fibre preform 11.
During process stage II, an aluminium alloy forming the matrix material 12 is cast around the fibre preform 11.
There is then produced an aluminium matrix composite material 13 which can be used as a bearing material, for a cyllnder barrell or a valve guide.
When the aluminium matrix composite material 13 is used as a bearing material as shown in Figure 2, it is proposed that the shaft 1 and the bearing bush 2 consist of aluminium alloys, for example that the shaft consists of a wrought aluminium alloy and the bearing bush of a cast aluminium alloy in the form of an infiltrated fibre preform, which means that materials of the same type are being paired. The outer casing 3 can consist of a pure matrix metal, for example of an easily weldable AlMgSi or AlZnMg alloy.
When the inventive material is used for a cylinder barrel, the paired materials as used for the piston 4 and the inliner 5 according to Figure 3 lead to improved sliding properties. For example, the piston 4 consists of aluminium and the cylinder barrel (inliner 5) of an infiltrated gradient material based on aluminium. There is no need for any clearances to be compensated for, because the outer layer of the infiltrated fibre preform features an almost identical thermal expansion behaviour to the outer piston face.
In the third application as illustrated in Figure 4, the valve seat and the valve 6 are produced from different materials. Whereas the valve material, for instance steel, must have very good strength properties and a high thermal resistance, the valve guide 7 is produced from an infiltrated gradient material with an aluminium matrix alloy. The wear behaviour of the latter can be adapted by means of the gradient structure to the wear behaviour of the valve shank 8.
As can be seen from the above examples, the engine-specific running properties and the engine-specific wear behaviour can be greatly improved by using the paired materials as described. It is to be expected that the running performance is considerably improved by the constant wear behaviour and the constant tolerance values.
Furthermore, oil consumption and thus emission behaviour are improved in those areas where the inventive composite materials are used. These expectations result from the knowledge that the tribological properties of the materials used and the emission behaviour are closely related to one another. Oil adhesion is improved as a result of the specific surface of the inventive composite materials.
The abrasion behaviour of the inventive composite materials is comparable to that of the nickel calcium silicate layers which comprise a very advantageous wear behaviour. The expansion behaviour is very similar to that of ceramic composites. By using oxidation-resistant alloys, infiltration of the fibre preform is so advantageous that it is correct to speak of complete wetting of the composite materials.
To achieve a specific structure of the inventive composite materials it is also possible to use directed fibre structures; they are directed magnetically into a predetermined shape. In this way it is possible to produce any shape of asymmetric fibre preforms whose individual fibres are orientated into the direction where the load is applied.
In spite of the large number of applications and the different possible alloy compositions in the infiltrated fibre preform and in the matrix, the inventive composite materials can be very easily recycled. The previously required complicated cleansing operations and procedures of separating non-ceramic fibres no longer have to be carried out.
The extreme case referred to above can be explained with the help of the following example:
When used for the cylinder barrels of a single- or multi-cylinder engine, the inventive aluminium matrix composite material can be provided with particularly advantageous properties when tolerances and clearances have to be compensated for. By using the same type of material (infiltration material) for cylinder sleeve faces and outer piston faces, no dimensional deviations between the used materials have been identified, neither when cold-starting an engine nor under continuous operating conditions, neither during acceleration cycles nor full throttle cycles. This means that also the emission behaviour of the inventive running faces of single- or multi-cylinder engines has been improved considerably over the entire operational range, as compared to conventionally produced composite materials reinforced by fully ceramic fibres.
A further advantage refers to the advantageous wetting behaviour during infiltration because the metallic and/or intermetallic fibres can be wetted particularly easily by an aluminium casting alloy, i.e. also in a pressure-less way. This is particularly important in connection with automated processes, for example in the case of pressure die casting processes, because the individual process stages can take place in a relatively short time while nevertheless ensuring complete wetting of the fibres of the fibre preform. Satisfactory wetting means that the die is well filled and that the fibre preform is well anchored in the matrix, so that the dimensional stability of the composite material in accordance with the invention is at least twice as high as that of a conventionally die-cast aluminium matrix material with oxide-ceramic fibres.
As a result of the improved dimensional stability of the fibre preform it is also possible to achieve high production speeds when using modern production processs.
For instance, it is possible to speed up the injecting sequence while simultaneously increasing the injection pressure during the pressure die casting process, so that, while the number of rejects is reduced, the production output is more than three times as high as that of comparable composite materials based on ceramics.
The proportion of fibres of the inventive aluminium matrix composite material can be adapted to the loads applied in the respective application. It is thus possible to produce new composite materials with a gradient structure and specific strength/elongation properties. Production costs are thus reduced, especially in the case of components with complicated shapes.
Comprehensive machining operations on the working surface with the improved rheological properties can be avoided if the part is designed accordingly. The process in accordance with the invention makes it possible to provide a component with both highly loaded sliding faces and temperature-loaded sealing faces, e.g. in the cylinder head region. Even tensioned parts with an improved elongation behaviour can be produced by a cost-effective overall process.
Decisive factors in this context are the structure, design and composition of the fibre preform which may comprise anopen-pore metallic structure in the porosity range of 30 - 97% with pore sizes of 1 ~ to 3 mm.
Furthermore, the surface roughness of the porous structure can be varied, which means that the ability of the melt to infiltrate the porous structure can be influenced. It is thus possible to achieve very good mechanical anchoring of the fibres with the help of a rough structure, whereas with a smooth fibre surface, the porous structure can be infiltrated more easily.
As the inventive aluminium matrix composite material consists of constituents of the same type, it has a homogeneous strength structure which results in a very good thermal shock behaviour, and since, furthermore, because of its metallic basis, its thermal conductivity reaches very high values, it is particularly suitable for being used in internal combustion engines. In addition, it is very suitable for chip-forming and non-chip-forming machining operations, especially in the transition zone between purely metallic and aluminium matrix composite materials, which so far led to problems due to different material structures.
To be able to use cylinder barrels made of composite materials it is necessary for the expansion coefficient of the shaped fibre members to be largely adapted to the matrix material and the base alloy. This has been achieved for the first time with the aluminium matrix composite material in accordance with the invention because the shaped fibre member consisting of a metallic and/or intermetallic fibre material can be largely adapted to its metallic environment by changing its composition. Porous ceramic structures, on the other hand, have a very limited spectrum of properties.
For optimising the wear properties, there are available the base materials of iron and nickel or the intermetallics such as iron-, nickel-, titanium-aluminides, tungsten, copper, cobalt, magnesium. Depending on requirements, it is possible, by selecting a suitable combination, advantageously to combine specific properties such as low density, good thermal conductivity, good corrosion resistance and good machining properties.
In addition to selecting the material, it is possible in the case of the aluminium matrix composite material, to achieve a gradient structure in the fibre preform.
For example, said member may comprise a rising or falling porosity or a rising or falling pore size across its cross-section. In this way it is possible to ensure that the properties of the metal matrix fibre composite meet the load requirements.
Below, there will be described an example of producing the inventive aluminium matrix composite material and some specific preferred applications which demonstrate the inventive idea and reveal further advantageous properties. In particular, reference is made to using the above material as a bearing material according to Figure 2, for a cylinder barrel according to Figure 3, and for a valve seat according to Figure 4.
As can be seen in Figure 1, process stage I, first a shaped fibre member 9 is connected, and provided with a firm structure, by being sintered in a furnace 10.
After the shaped fibre member has cooled down, it can be converted into a fibre preform 11.
During process stage II, an aluminium alloy forming the matrix material 12 is cast around the fibre preform 11.
There is then produced an aluminium matrix composite material 13 which can be used as a bearing material, for a cyllnder barrell or a valve guide.
When the aluminium matrix composite material 13 is used as a bearing material as shown in Figure 2, it is proposed that the shaft 1 and the bearing bush 2 consist of aluminium alloys, for example that the shaft consists of a wrought aluminium alloy and the bearing bush of a cast aluminium alloy in the form of an infiltrated fibre preform, which means that materials of the same type are being paired. The outer casing 3 can consist of a pure matrix metal, for example of an easily weldable AlMgSi or AlZnMg alloy.
When the inventive material is used for a cylinder barrel, the paired materials as used for the piston 4 and the inliner 5 according to Figure 3 lead to improved sliding properties. For example, the piston 4 consists of aluminium and the cylinder barrel (inliner 5) of an infiltrated gradient material based on aluminium. There is no need for any clearances to be compensated for, because the outer layer of the infiltrated fibre preform features an almost identical thermal expansion behaviour to the outer piston face.
In the third application as illustrated in Figure 4, the valve seat and the valve 6 are produced from different materials. Whereas the valve material, for instance steel, must have very good strength properties and a high thermal resistance, the valve guide 7 is produced from an infiltrated gradient material with an aluminium matrix alloy. The wear behaviour of the latter can be adapted by means of the gradient structure to the wear behaviour of the valve shank 8.
As can be seen from the above examples, the engine-specific running properties and the engine-specific wear behaviour can be greatly improved by using the paired materials as described. It is to be expected that the running performance is considerably improved by the constant wear behaviour and the constant tolerance values.
Furthermore, oil consumption and thus emission behaviour are improved in those areas where the inventive composite materials are used. These expectations result from the knowledge that the tribological properties of the materials used and the emission behaviour are closely related to one another. Oil adhesion is improved as a result of the specific surface of the inventive composite materials.
The abrasion behaviour of the inventive composite materials is comparable to that of the nickel calcium silicate layers which comprise a very advantageous wear behaviour. The expansion behaviour is very similar to that of ceramic composites. By using oxidation-resistant alloys, infiltration of the fibre preform is so advantageous that it is correct to speak of complete wetting of the composite materials.
To achieve a specific structure of the inventive composite materials it is also possible to use directed fibre structures; they are directed magnetically into a predetermined shape. In this way it is possible to produce any shape of asymmetric fibre preforms whose individual fibres are orientated into the direction where the load is applied.
In spite of the large number of applications and the different possible alloy compositions in the infiltrated fibre preform and in the matrix, the inventive composite materials can be very easily recycled. The previously required complicated cleansing operations and procedures of separating non-ceramic fibres no longer have to be carried out.
Claims (21)
1. An aluminium matrix composite material consisting of a porous fibre preform which is embedded in an aluminium alloy and which has a higher strength and an improved wear behaviour as compared to the aluminium matrix, characterised in that the fibre preform consists of a shaped fibre member which comprises a metallic and/or intermetallic structure and into which there is infiltrated a silicon-containing aluminium alloy melt, with the Si-content of the melt amounting to 5 - 14 % by weight.
2. An aluminium matrix composite material according to claim 1, characterised in that the fibres of the shaped fibre member are connected by being sintered at the points of intersection.
3. An aluminium matrix composite material according to any one of the preceding claims, characterised in that the composite material comprises at least one working surface with an improved wear behaviour, with the embedded fibre preform, on its side pointing towards the working surface, having lower porosity values than on the side of the composite material facing away from the working surface.
4. An aluminium matrix composite material according to any one of the preceding claims, characterised in that the working surface is formed by the preform structure of the composite material.
5. An aluminium matrix composite material according to any one of the preceding claims, characterised in that the preform structure, if viewed across its cross-section, comprises a gradient, with the porosity values ranging between 20 and 98 %.
6. An aluminium matrix composite material according to any one of the preceding claims, characterised in that the preform contains homogeneous regions with a porosity ranging between 20 and 98%.
7. An aluminium matrix composite material according to any one of the preceding claims, characterised in that the preform is layered, having a supporting layer with a coarse-pore preform structure and an outer layer with a fine-pore preform structure, which layers are sintered together at the points of intersection.
8. An aluminium matrix composite material according to any one of the preceding claims, characterised in that the layers consist of fibres with different chemical and physical properties.
9. An aluminium matrix composite material according to any one of the preceding claims, characterised in that the fibre preform consists of fibres of an iron chromium aluminium alloy which is insensitive to oxidation, with Fe = 50 - 85 % by weight, Cr = 10 - 30 %
by weight, A1 = 5 - 20 % by weight, from which alloy there were obtained, by melt extraction, individual threads of a length L = 0.5 - 5 mm with a fibre diameter of 1 - 50 µm.
by weight, A1 = 5 - 20 % by weight, from which alloy there were obtained, by melt extraction, individual threads of a length L = 0.5 - 5 mm with a fibre diameter of 1 - 50 µm.
10. An aluminium matrix composite material according to any one of the preceding claims, characterised in that for producing melt-extracted fibres, use is made of an aluminium nickel alloy with aluminium contents of 7 up to 40%.
11. An aluminium matrix composite material according to any one of the preceding claims, characterised in that the fibres are produced from an iron nickel aluminium alloy.
12. An aluminium matrix composite material according to any one of the preceding claims, characterised in that the fibres of the shaped fibre member consist of intermetallic aluminides of type AlFe, AlTi, AlNi.
13. A process of producing aluminium matrix composite materials consisting of a porous fibre preform into which an aluminium alloy was infiltrated, characterised in that the fibres of the fibre preform are produced by a melt extraction process, are processed to obtain a homogenous or gradient structure and are connected by sintering to form a firm, porous preform;
that the fibre preform is pre-heated to a temperature of > 200 °C; and that subsequently, a silicon-containing aluminium casting alloy melt is infiltrated into the fibre preform.
that the fibre preform is pre-heated to a temperature of > 200 °C; and that subsequently, a silicon-containing aluminium casting alloy melt is infiltrated into the fibre preform.
14. A. process according to any one of the preceding claims, characterised in that the fibre preform is provided in the form of a shaped fibre member with a specific fibre orientation of the metallic fibres, with the points of intersection being sintered.
15. A process according to the preceding claim, characterised in that infiltration takes place in accordance with the gravity casting process.
16. A process according to any one of the preceding claims, characterised in that infiltration takes place in accordance with the pressure die casting process at a gating speed of >
5m/sec.
5m/sec.
17. A process according to any one of the preceding claims, characterised in that a pressure die casting alloy is infiltrated into the fibre preform in a pressure die casting die at a minimum pressure of 80 bar.
18. A process according to any one of the preceding claims, characterised in that the fibre preform comprises an open porosity of 20 - 98 %, with porosity being controlled by the fibre geometry and the fibre orientation during the layering operation.
19. A process according to any one of the preceding claims, characterised in that the pore size of the fibre preform is determined by the fibre content per unit of volume of the preform, ranging from 20 µm to 1000 µm.
20. A process according to any one of the preceding claims, characterised in that infiltration takes place during a pressure-assisted casting process, with the pressure being maintained until a diffusion zone has formed between the fibre material and the matrix.
21. A process according to any one of the preceding claims, characterised in that while aluminium melt is being infiltrated, or after aluminium melt has been infiltrated, a matrix material is cast around the fibre preform, which matrix material is selected from one one or several metals of the following group:
aluminium silicon magnesium zinc (casting materials) in combination with the intermetallics of iron-, nickel-, titanium-aluminides tungsten, copper, cobalt and/or magnesium.
aluminium silicon magnesium zinc (casting materials) in combination with the intermetallics of iron-, nickel-, titanium-aluminides tungsten, copper, cobalt and/or magnesium.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE19712624A DE19712624C2 (en) | 1997-03-26 | 1997-03-26 | Aluminum matrix composite and process for its manufacture |
DE19712624.3-24 | 1997-03-26 |
Publications (1)
Publication Number | Publication Date |
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CA2232177A1 true CA2232177A1 (en) | 1998-09-26 |
Family
ID=7824630
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
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CA002232177A Abandoned CA2232177A1 (en) | 1997-03-26 | 1998-03-16 | Aluminium matrix composite material and process of producing same |
Country Status (7)
Country | Link |
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EP (1) | EP0867517B1 (en) |
JP (1) | JPH10265870A (en) |
AT (1) | ATE194170T1 (en) |
BR (1) | BR9806333A (en) |
CA (1) | CA2232177A1 (en) |
DE (2) | DE19712624C2 (en) |
HU (1) | HU216623B (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2014096376A1 (en) * | 2012-12-21 | 2014-06-26 | Jaguar Land Rover Limited | Component comprising a metal matrix reinforcement member and method of formation thereof |
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DE19909675B4 (en) * | 1999-03-05 | 2005-07-14 | Mtu Aero Engines Gmbh | Layer structure and method for its production |
DE60032728T2 (en) * | 1999-08-10 | 2007-04-26 | NHK Spring Co., Ltd., Yokohama | PISTON WITH A METALLIC COMPOSITE |
DE10012787B4 (en) * | 2000-03-16 | 2008-04-10 | Volkswagen Ag | Process for producing light metal castings with cast-in bushings |
DE10121928A1 (en) * | 2001-05-05 | 2002-11-14 | Univ Friedrich Alexander Er | Production of locally reinforced light metal parts comprises placing porous reinforcing element made from sintered ceramic with sponge-like structure on the site to be reinforced in die casting mold, and infiltrating with melt |
KR20030000544A (en) * | 2001-06-26 | 2003-01-06 | 현대자동차주식회사 | cylinder head with valve seat and a preparing method thereof |
DE10133757A1 (en) * | 2001-07-11 | 2003-02-13 | Mahle Ventiltrieb Gmbh | Use as the base area of a cylinder head |
DE10157478A1 (en) * | 2001-11-23 | 2003-06-05 | Fne Gmbh | Compound metal material is a shaped first metal, e.g. a wire coil, embedded in a ground matrix of the second metal. |
DE10251426A1 (en) * | 2002-11-05 | 2004-05-13 | Volkswagen Ag | Method for casting a sleeved cylinder block for IC engine with the sleeve prepared from high quality sintered material with a coarse outer surface to bond to the cast block |
DE102004005799A1 (en) * | 2004-02-06 | 2005-09-01 | Daimlerchrysler Ag | Method for producing a local reinforcement for a component of an internal combustion engine |
DE102004039306A1 (en) * | 2004-08-12 | 2006-02-23 | Bayerische Motoren Werke Ag | Process to manufacture automotive crankcase with embedded supra-eutectic lightweight metal containing silicon |
DE102005043193A1 (en) * | 2005-09-09 | 2007-03-15 | Ks Aluminium-Technologie Ag | Cylinder crankcase for motor vehicles |
DE102006007148A1 (en) * | 2006-02-16 | 2007-08-30 | Volkswagen Ag | Piston for internal combustion engines and method for producing a piston for internal combustion engines |
JP5185178B2 (en) | 2009-03-31 | 2013-04-17 | トヨタ自動車株式会社 | MMC cylinder liner and manufacturing method thereof |
BR112012012525A2 (en) * | 2009-12-01 | 2019-09-24 | Applied Nanostructured Sols | electrical matrix composite materials containing carbon nanotube infused fiber materials and methods for their production |
CA2785803A1 (en) | 2010-02-02 | 2011-11-24 | Applied Nanostructured Solutions, Llc | Carbon nanotube-infused fiber materials containing parallel-aligned carbon nanotubes, methods for production thereof, and composite materials derived therefrom |
US9017854B2 (en) | 2010-08-30 | 2015-04-28 | Applied Nanostructured Solutions, Llc | Structural energy storage assemblies and methods for production thereof |
JP2013027936A (en) * | 2012-10-24 | 2013-02-07 | Tpr Co Ltd | Support member |
DE102013215020A1 (en) | 2013-07-31 | 2015-02-05 | Mahle International Gmbh | Infiltratable insert |
CN107841659A (en) * | 2017-10-27 | 2018-03-27 | 黄林海 | A kind of preparation method of high-strength corrosion-resisting Al alloy composite |
JP7381011B2 (en) * | 2019-10-26 | 2023-11-15 | 株式会社フジキン | safety valve |
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DE3025636A1 (en) * | 1980-07-07 | 1982-02-04 | Alfred Teves Gmbh, 6000 Frankfurt | MOLDED WORKPIECE |
GB2106433B (en) * | 1981-09-22 | 1985-11-06 | Ae Plc | Squeeze casting of pistons |
DE3418405A1 (en) * | 1983-05-18 | 1984-11-29 | Mazda Motor Corp., Hiroshima | Method for the production of castings from aluminium alloy and of pistons composed of an aluminium alloy |
DE3404092C1 (en) * | 1984-02-07 | 1985-06-13 | Daimler-Benz Ag, 7000 Stuttgart | Process for the production of fiber-reinforced light metal castings by die casting |
JPS61166935A (en) * | 1985-01-18 | 1986-07-28 | Mazda Motor Corp | Composite member superior in wear resistance and its manufacture |
JPS6267132A (en) * | 1985-09-19 | 1987-03-26 | Nippon Kokan Kk <Nkk> | Production of composite metallic material |
EP0271222A3 (en) * | 1986-11-12 | 1989-07-12 | Alcan International Limited | Production of metal matrix composites |
BR8700527A (en) * | 1987-01-29 | 1988-08-16 | Metal Leve Sa | PUMP AND PUMP MANUFACTURING PROCESS FOR INTERNAL COMBUSTION ENGINES |
JP2909545B2 (en) * | 1988-04-30 | 1999-06-23 | トヨタ自動車株式会社 | Manufacturing method of metal matrix composite material |
JPH0636984B2 (en) * | 1990-04-27 | 1994-05-18 | 東海カーボン株式会社 | Method for manufacturing partial composite member |
DE4115057A1 (en) * | 1991-05-08 | 1992-11-12 | Austria Metall | METHOD AND DEVICE FOR INFILTRATING MOLTEN METAL |
DE4328619C2 (en) * | 1993-08-26 | 1995-08-10 | Peak Werkstoff Gmbh | Partially reinforced cast aluminum component and process for its production |
GB9414660D0 (en) * | 1994-07-20 | 1994-09-07 | Gkn Sankey Ltd | An article and method for its production |
-
1997
- 1997-03-26 DE DE19712624A patent/DE19712624C2/en not_active Expired - Fee Related
-
1998
- 1998-01-31 DE DE59800182T patent/DE59800182D1/en not_active Expired - Fee Related
- 1998-01-31 AT AT98101659T patent/ATE194170T1/en not_active IP Right Cessation
- 1998-01-31 EP EP98101659A patent/EP0867517B1/en not_active Expired - Lifetime
- 1998-03-16 CA CA002232177A patent/CA2232177A1/en not_active Abandoned
- 1998-03-23 JP JP10093973A patent/JPH10265870A/en active Pending
- 1998-03-25 HU HU9800652A patent/HU216623B/en not_active IP Right Cessation
- 1998-03-25 BR BR9806333-2A patent/BR9806333A/en not_active Application Discontinuation
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2014096376A1 (en) * | 2012-12-21 | 2014-06-26 | Jaguar Land Rover Limited | Component comprising a metal matrix reinforcement member and method of formation thereof |
CN104870124A (en) * | 2012-12-21 | 2015-08-26 | 捷豹路虎有限公司 | Component comprising a metal matrix reinforcement member and method of formation thereof |
Also Published As
Publication number | Publication date |
---|---|
HUP9800652A1 (en) | 1998-10-28 |
HU216623B (en) | 1999-07-28 |
EP0867517A1 (en) | 1998-09-30 |
DE59800182D1 (en) | 2000-08-03 |
ATE194170T1 (en) | 2000-07-15 |
JPH10265870A (en) | 1998-10-06 |
BR9806333A (en) | 1999-12-14 |
EP0867517B1 (en) | 2000-06-28 |
MX9802324A (en) | 1998-12-31 |
DE19712624C2 (en) | 1999-11-04 |
HU9800652D0 (en) | 1998-05-28 |
DE19712624A1 (en) | 1998-10-01 |
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