Machinable metal matrix composite and method for making the same

Abstract

A metal matrix composite comprises and/or consists of a uniform distribution of calcined ceramic particles having an average particle size of between 0.30 and 0.99 microns and a metal or alloy uniformly distributed with the ceramic particles and wherein the ceramic particles include oxides of two separate metals selected from the group consisting of Al, Li, Be, Pb, Fe, Ag, Au, Sn, Mg, Ti, Cu, and Zn, and in which said ceramic particles comprise at least 15 volume percent of the metal matrix sintered together and wherein said metal-matrix being machinable with a high speed steel (HSS) bit for greater than about one minute without excessive wear to the bit.

Claims

1. A metal-matrix composite comprising: a substantially uniform distribution of ceramic particles having an average particle size of between 0.35 and 0.99 microns and a meso-structure of less than 200 microns; and a metal substantially uniformly distributed between the ceramic particles, wherein the metal comprises aluminum, magnesium, or a mixture or alloy thereof; wherein the ceramic particles comprise a mixture of at least aluminum oxide (Al.sub.2O.sub.3) and magnesium oxide (MgO), and wherein the ceramic particles are chemically stable in the metal at a temperature above a melting point of the metal; wherein the metal-matrix composite is no greater than 85% by volume the metal and no less than 15% by volume the ceramic particles, and wherein the ceramic particles are prepared from a ceramic precursor material that is batched according to the following recipe: TABLE-US-00003 Material Per Batch (lbs.) Almatis Calcined Alumina 100.0 A-1000 SG Magchem 10 MgO 325 0.05 Carbon Black N990 22.9 Graphite M-450 31.5 Organic Binders 5.2 Water 82.1 wherein the (Al.sub.2O.sub.3) and MgO are dispersed in de-ionized water to form a first slurry, the first slurry is then milled until an (Al.sub.2O.sub.3) particle size of about 0.5 micron is obtained in a second slurry, the carbon black and the graphite, are then dispersed in the second slurry and milled to obtain a third slurry, after which the organic binders are added to the third slurry to obtain a fourth slurry which is then milled to obtain a final slurry, the final slurry is then dried and pressed into a preform shape and subjected to a thermal treatment process to obtain a ceramic preform having about 65% by volume open cell porosity, the ceramic preform is then placed into an infiltration vessel, along with a volume of the metal, and heated, in a non-oxidizing atmosphere, to a temperature above a melting point of the metal to obtain a molten metal; and a gas pressure is then increased in the infiltration vessel to reach an infiltration pressure sufficient to force the molten metal into the ceramic preform and obtain the metal-matrix composite.

2. The metal-matrix composite according to claim 1, wherein: at least 90 percent of the ceramic particles are uniformly distributed on a scale of two (2) times the average ceramic particle size.

3. The metal-matrix composite according to claim 1, wherein the ceramic particles have an aspect ratio of no greater than about 2:1.

4. The metal-matrix composite according to claim 1, wherein the metal-matrix composite has a tensile modulus which is at least 30 percent greater than the tensile modulus of the metal.

5. The metal-matrix composite according to claim 1, wherein the metal-matrix composite has a tensile strength of at least twice that of the metal and retains a 2:1 tensile strength ratio up to a temperature of about one-half of a melting point of the metal.

6. The metal-matrix composite according to claim 1, wherein the thermal treatment process comprises maintaining the preform shape at a treatment temperature above 750 degrees C. for a treatment period of at least 24 hours.

7. The metal-matrix composite according to claim 1, wherein at least 80% of the ceramic particles are substantially uniformly distributed on a scale of three times the particle size; and wherein the ceramic particles have an aspect ratio no greater than about 3:1.

8. The metal-matrix composite according to claim 7, wherein the ceramic particles comprise magnesium oxide (MgO) particles that where produced by dehydrating magnesium hydroxide (Mg(OH).sub.2).

9. The metal-matrix composite according to claim 7, wherein the final slurry is spray dried under conditions to form spray dried particles having a median particle size of less than 200 microns.

10. The metal-matrix composite according to claim 7, wherein the ceramic particles include magnesium oxide particles that were produced by dehydrating magnesium hydroxide (Mg(OH).sub.2) particles.

11. A metal-matrix composite comprising: a substantially uniform distribution of ceramic particles having an average particle size of between 0.35 and 0.99 microns; and a metal substantially uniformly distributed between the ceramic particles, wherein the metal comprises aluminum, magnesium, or a mixture or alloy thereof; wherein the ceramic particles comprise a mixture of at least aluminum oxide (Al.sub.2O.sub.3) and magnesium oxide (MgO) and wherein the ceramic particles are chemically stable in the metal at a temperature above a melting point of the metal; wherein the metal-matrix composite is no greater than 85% by volume the metal and no less than 15% by volume the ceramic particles, and wherein the ceramic particles are prepared from a ceramic precursor material that is batched according to the following recipe: TABLE-US-00004 Material Per Batch (lbs.) Particulate Oxides 100.0 Carbon Black N990 22.9 Graphite 31.5 Organic Binders 5.2 Water 82.1 wherein the particulate oxides, the carbon black, the graphite, and the organic binders are dispersed in water and milled to form a slurry having an Al.sub.2O.sub.3 particle size of about 0.5 micron, the slurry is then dried and pressed into a preform shape; the preform shape is then subjected to a thermal treatment process to produce a ceramic preform having about 65% by volume open cell porosity, the ceramic preform is then placed into an infiltration vessel, along with a volume of the metal and heated to an infiltration temperature above a melting point of the metal to obtain a molten metal; and the molten metal is then forced into the open cell porosity of the ceramic preform under an infiltration pressure and then cooled to obtain the metal-matrix composite.

12. The metal-matrix composite according to claim 11, wherein: the ceramic particles comprise no more than about 35 vol % of the metal-matrix composite and wherein at least 80 percent of the ceramic particles are uniformly distributed on a scale of three times the average ceramic particle size.

13. The metal-matrix composite according to claim 11, wherein the ceramic particles have an aspect ratio of no greater than about 3:1.

14. The metal-matrix composite according to claim 11, wherein the metal-matrix composite has a ductility of at least about 30 percent of the ductility for the metal and wherein the ceramic particles further comprise an oxide of an additional metal selected from the group consisting of Li, Be, Pb, Fe, Ag, Au, Sn, Ti, Cu, and Zn, and in which the ceramic particles comprise at least 15 volume percent of the metal matrix composite.

15. The metal-matrix composite according to claim 11, wherein the metal-matrix composite has a tensile strength of at least twice that of the metal at temperatures up to about one-half the melting point of the metal.

16. The metal-matrix composite according to claim 11, wherein the metal-matrix composite has a tensile modulus which is at least about 30 percent greater than the tensile modulus of the metal.

17. The metal-matrix composite according to claim 11, wherein: the ceramic particles further comprise an additional oxide, boride, nitride, carbide, carbonate, or a combination thereof; and the metal further comprises a minor portion of an additional metal selected from the group consisting of Li, Be, Pb, Fe, Ag, Au, Sn, Ti, Cu, Zn, or a mixture or alloy thereof.

Description

BRIEF DESCRIPTION OF THE DRAWINGS

(1) Aspects of the present disclosure are best understood from the following detailed description when read with the accompanying FIGURES. It is noted that, in accordance with the standard practice in the industry, various features are not drawn to scale. In fact, the dimensions of the various features may be arbitrarily increased or reduced for clarity of discussion.

(2) FIG. 1 is a graphical illustration of the heating steps for forming a metal matrix composition in accordance with an embodiment of the present invention.

DETAILED DESCRIPTION

(3) The following disclosure provides many different embodiments, or examples, for implementing different features of the provided subject matter. Specific examples of components, values, operations, materials, arrangements, or the like, are described below to simplify the present disclosure. These are, of course, merely examples and are not intended to be limiting. Other components, values, operations, materials, arrangements, or the like, are contemplated. For example, the formation of a first feature over or on a second feature in the description that follows may include embodiments in which the first and second features are formed in direct contact, and may also include embodiments in which additional features may be formed between the first and second features, such that the first and second features may not be in direct contact. In addition, the present disclosure may repeat reference numerals and/or letters in the various examples. This repetition is for the purpose of simplicity and clarity and does not in itself dictate a relationship between the various embodiments and/or configurations discussed.

(4) In the following embodiments of the invention, at least one embodiment is illustrated by the second embodiment. Other embodiments are shown by Examples 1, 3 and 4. To be more specific, Example 1 is an embodiment of the present invention which comprises a 65% by volume 6061 aluminum with a reinforcement of 35% by volume of alumina (Al2O3). The ceramic precursor material is typically batched according to the following recipe:

Example 1

(5) TABLE-US-00001 Material Per Batch (lbs.) Almatis Calcined Alumina 100.0 A-1000 SG Magchem 10 MgO 325 0.05 Carbon Black N990 22.9 Graphite M-450 31.5 Organic Binders 5.2 Water 82.1

(6) Alumina (Al2O3) and/or magnesium oxide (MgO) are dispersed in de-ionized water in a mixing tank while constantly mixing, the primary slurry is then milled until an alumina (Al2O3) particle size of about 0.5 micron is obtained, and then the carbon black is added followed by the graphite into the primary slurry and the entire mixture milled for about another 8 hours, additional binders are added to the secondary slurry which is milled for an additional 4 hours, and then dried. The dried powder is pressed into a desired shape (preform) then fired in a kiln according to the steps in FIG. 1.

(7) The fired alumina preform, which is about 65% by volume inter-connected porosity and placed into a crucible along with 6061 aluminum, all of which is heated under vacuum to a temperature of about 750° C. in a pressure infiltration vessel and the resulting liquid aluminum is then squeezed into the preform by gradually applying inert gas pressure to about 2000 psi and subsequently cooled to room temperature.

(8) Example 2 comprises a composite matrix of 65% by volume aluminum 6061 and a reinforcement of 30% by volume alumina (Al2O3) and about 5% by volume magnesium oxide (MgO). The batching recipe, is the same as in Example 1 except in Example 2 (preferred embodiment) there is 86 pounds of alumina and 13 pounds of magnesium oxide and the firing and infiltration processes are the same as in Example 1.

(9) In Example 3, the composite matrix contains 65% by volume AZ31B magnesium and the reinforcement is 30% by volume magnesium oxide (MgO), 5% by volume alumina (Al2O3) reinforcement and the batching recipe and the firing and infiltration processes are the same as in Example 2 except in Example 3 there is 14 pounds of alumina (Al2O3) and 79 pounds of magnesium oxide (MgO).

(10) Example 4 has a composite matrix of 65% by volume AZ31B magnesium and the reinforcement is 35% by volume magnesium oxide (MgO) and the batching recipe and the firing and infiltration processes are the same as in Example 1 except alumina is 0 pounds and magnesium oxide is 92 pounds.

(11) Particularly attractive finished products are light weight, strong and stiff such as pistons, connecting rods and rocker arms for internal combustion engines and brake components made from the composite, for Example 1. Pistons and brake components made from composite, Example 3, additionally offer exceptionally low weight.

(12) It should also be recognized that the composites of the Examples have a tensile modulus which is at least 30 to 200% greater than the tensile modulus of the metal and wherein the metal ceramic composite has a ductility of at least about 30% of the ductility of the metal and wherein the composite has a tensile strength of at least twice that of the metal and retains the tensile strength ratio at temperatures up to about one-half the melting point of the metal and in which the metal matrix composite is machinable with a high-strength steel bit for greater than about one minute without serious damage to the bit.

(13) A metal-matrix composite comprising a uniform or substantially uniform distribution of calcined ceramic particles having an average particle size of less than about one micron and a metal or alloy substantially uniformly distributed with the ceramic particles and a meso-structure of less than 200 microns.

(14) In a fifth embodiment of the invention at least about 80 percent of the ceramic particles are uniformly distributed on a scale of three (3) times the particle size.

(15) In a sixth embodiment of the invention at least 90 percent of the ceramic particles are uniformly distributed on a scale of two (2) times the particle size.

(16) In a seventh embodiment of the invention the ceramic particles have an aspect ratio of no greater than about three to one (3:1).

(17) Further, in an eighth embodiment of the invention the ceramic particles have an aspect ratio of no greater than about two to one (2:1).

(18) In a ninth embodiment of the invention the composite has a tensile modulus which is at least thirty (30) to two hundred (200) percent greater than the tensile modulus of said metal.

(19) In a tenth example of the invention the metal-matrix composite has a tensile strength of at least twice of said metal and retains said tensile strength ratio at temperatures up to about one-half the melting point of said metal.

(20) According to an eleventh embodiment and/or example of the metal-matrix composite, the metal-ceramic composite has a ductility of at least about 30 percent of the ductility of said metal and in which said metal-matrix composite comprises a uniform distribution of calcined ceramic particles having an average particle size of between 0.35 and 0.99 microns and a metal or alloy substantially uniformly distributed with said ceramic particles and in which said ceramic particles include oxides of two (2) separate metals selected from the group consisting of Al, Li, Be, Pb, Fe, Ag, Au, Sn, Mg, Ti, Cu, and Zn, and in which said ceramic particles comprise at least 15 volume percent of the metal matrix and wherein the metal-matrix composite being machinable with a high speed steel (HSS) bit for greater than about one (1) minute without excessive wear to said bit.

(21) In Example 12, the metal-matrix composite has a tensile strength of at least twice that of the metal and retains said tensile strength ratio at temperatures up to about one-half the melting point of said metal.

(22) In Example 13, the metal-matrix composite in which the metal matrix composite is machinable with a high-speed steel bit for greater than about one (1) minute without excessive wear to the bit.

(23) In Example 14, the metal-matrix composite wherein the composite has a tensile modulus which is at least about thirty (30) to two hundred (200) percent greater than the tensile modulus of the metal.

(24) Example 15 is a metal-matrix composite wherein a uniform or substantially uniform distribution of calcined ceramic particles have an average particle size of no greater than about one (1) micron and a metal or alloy substantially uniform and distributed with the ceramic particles and a meso-structure of less than 200 microns in which the ceramic particles comprise at least about 15 volume percent of the metal-matrix and in which the ceramic particles are thermally stable in the metal-matrix.

(25) In embodiment 16, the metal-matrix composite wherein the ceramic particles are chemically stable in the molten metal or alloy.

(26) In Example 17, the metal-matrix composite in which the ceramic particles comprise an oxide, boride, nitride, carbide, carbon or a combination thereof and a metal or alloy substantially uniformly distributed with the ceramic particles, the metal or alloy comprising Al, Li, Be, Pb, Fe, Ag, Au, Sn, Mg, Ti, Cu, Zn, or a mixture thereof.

(27) In Example 18, the metal-matrix composite in which the metal is selected from the group consisting of aluminum, magnesium and mixtures thereof and the reinforcement is selected from the group consisting of alumina (Al2O3), magnesium oxide (MgO) and mixtures thereof and wherein the composite is 65% by volume 6061 aluminum and 35% by volume a mixture of alumina and magnesia (MgO), and wherein the ceramic precursor material is batched according to the following recipe:

(28) TABLE-US-00002 Material Per Batch (lbs.) Almatis Calcined Alumina 100.0 A-1000 SG Magchem 10 MgO 325 0.05 Carbon Black N990 22.9 Graphite M-450 31.5 Organic Binders 5.2 Water 82.1

(29) Alumina (Al2O3) and/or magnesium oxide (MgO) is dispersed in de-ionized water in a mixing tank while constantly mixing and the primary slurry is then milled until an alumina (Al2O3) particle size of about 0.5 micron is obtained, and the carbon black, followed by the graphite, is dispersed in a primary slurry and a resulting mixture milled for about 8 hours, additional binders are added to the secondary slurry which are milled for an additional 8 hours plus 4 hours, dried and pressed into a desired shape and then fired in a kiln according to the steps in FIG. 1.

(30) The fired alumina preform, which is ˜65% by volume inter-connected porosity, is then placed into a crucible, along with the 6061 aluminum, all of which is heated under vacuum to a temperature of ˜750 degrees C. in a pressure infiltration vessel. The resulting liquid aluminum is then squeezed into the preform by gradually applying inert gas pressure to ˜2000 psi. The resulting billet is then cooled to room temperature.

(31) In Example 19, a metal-matrix composite comprising a uniform or substantially uniform distribution of calcined ceramic particles having an average particle size of between 0.35 and 0.99 microns and a metal or alloy substantially uniformly distributed with the ceramic particles and a meso-structure of less than 200 microns in which the ceramic particles comprise at least 15 volume percent of the metal-matrix and the metal-matrix composites being machinable with a high-speed steel (HSS) for greater than about one (1) minute without excessive wear to the bit and in which the metal is selected from the group consisting of aluminum and magnesium and mixtures thereof; and wherein at least 80% of the ceramic particles are uniformly distributed on a scale of three times the particle size; and in which the ceramic particle have an aspect ratio of no greater than about three to one (3:1).

(32) While one or more embodiments of the present invention have been described in connection with its preferred embodiments it should be recognized that changes and modifications may be made therein without departing from the scope of the appended claims.

(33) In Example 20, the magnesium oxide (MgO) in Examples 1 through 19 is obtained by first batching the mixes with magnesium hydroxide (Mg(OH)2) rather than magnesium oxide (MgO) which is then converted to magnesium oxide (MgO), after pressing into a preform, by dehydration of the magnesium hydroxide (Mg(OH)2).

(34) In Example 20, batching with magnesium hydroxide (Mg(OH)2) is substituted in place of batching with magnesium oxide (MgO) in all embodiments of the invention.