Method of making aluminum or magnesium based composite engine blocks or other parts with in-situ formed reinforced phases through squeeze casting or semi-solid metal forming and post heat treatment
09999921 ยท 2018-06-19
Assignee
Inventors
- Yucong Wang (West Bloomfield, MI, US)
- Richard J. Osborne (Rochester, MI, US)
- Brian J. McClory (Royal Oak, MI, US)
Cpc classification
B22F5/008
PERFORMING OPERATIONS; TRANSPORTING
C22C1/1073
CHEMISTRY; METALLURGY
B22D17/08
PERFORMING OPERATIONS; TRANSPORTING
C22C1/1073
CHEMISTRY; METALLURGY
B22F2999/00
PERFORMING OPERATIONS; TRANSPORTING
C22C32/00
CHEMISTRY; METALLURGY
B22D27/20
PERFORMING OPERATIONS; TRANSPORTING
B22F2998/10
PERFORMING OPERATIONS; TRANSPORTING
B22F2998/10
PERFORMING OPERATIONS; TRANSPORTING
B22D17/007
PERFORMING OPERATIONS; TRANSPORTING
B22F2999/00
PERFORMING OPERATIONS; TRANSPORTING
B22D21/007
PERFORMING OPERATIONS; TRANSPORTING
B22D25/02
PERFORMING OPERATIONS; TRANSPORTING
International classification
B22D21/00
PERFORMING OPERATIONS; TRANSPORTING
B22D27/20
PERFORMING OPERATIONS; TRANSPORTING
B22D17/08
PERFORMING OPERATIONS; TRANSPORTING
B22D25/02
PERFORMING OPERATIONS; TRANSPORTING
Abstract
A method of making a reinforced metal alloy component, the method including introducing a reinforcing phase precursor into a bulk alloy that is selected from the group consisting of high-entropy alloys, aluminum-based alloys, magnesium-based alloys and combinations thereof. The precursor is converted to a reinforcing phase by exposing the bulk alloy and precursor to an elevated temperature during one or more of a subsequent heat treating step, squeeze casting shaping or semi-solid metal shaping.
Claims
1. A method of making a reinforced metal alloy component, said method comprising: introducing at least one reinforcing phase precursor into a bulk alloy that is selected from the group consisting of aluminum-based alloys, magnesium-based alloys, high-entropy alloys and combinations thereof; and forming said component as a composite of said bulk alloy and at least one reinforcing phase that is produced upon activation of said at least one reinforcing phase precursor by using either squeeze casting or semi-solid metal forming such that a linear dimension of said at least one reinforcing phase is in the nanometer to micrometer range.
2. The method of claim 1, wherein said activation comprises catalyzing said at least one reinforcing phase precursor by increasing the temperature of said bulk alloy above its solidus temperature.
3. The method of claim 2, wherein said activation further takes place in at least one subsequent heat treating step.
4. The method of claim 2, wherein said introducing by said squeeze casting comprises having said bulk alloy be in melted form at the time said at least one reinforcing phase precursor is added thereto.
5. The method of claim 4, wherein said forming comprises: maintaining said composite in a substantially melted form; placing said substantially melted composite into a shot sleeve; forcing said substantially melted composite into a substantially final shape die cavity; and maintaining an elevated pressure on said substantially melted composite until a final shape of said component defined by said final shape die cavity has substantially solidified.
6. The method of claim 5, wherein said substantially final shape die cavity is shaped to define an automobile component.
7. The method of claim 5, further comprising heat treating said component once it has been has substantially solidified.
8. The method of claim 1, wherein said activation comprises catalyzing said at least one reinforcing phase precursor by at least one of increasing the pressure on said reinforcing phase precursor, applying ultrasonic vibration to said reinforcing phase precursor and applying an electromagnetic field to said reinforcing phase precursor.
9. The method of claim 1, wherein said aluminum-based bulk alloy is selected from the group consisting of eutectic alloys, near-eutectic alloys, hypoeutectic alloys, hypereutectic alloys and forged alloys.
10. The method of claim 1, wherein said reinforcing phase defines a higher modulus of elasticity than said bulk alloy.
11. The method of claim 1, wherein said reinforcing phase is selected from the group consisting of ceramics, intermetallics, rare earth elements and dispersoids.
12. The method of claim 1, wherein said introducing by said semi-solid metal forming comprises providing said bulk alloy in particulate form at the time said at least one reinforcing phase precursor is introduced thereto.
13. The method of claim 12, wherein said forming comprises: introducing said composite into a substantially preliminary shape die cavity; and providing a combination of heat and pressure until a preliminary shape of said component defined by said preliminary shape die cavity has substantially solidified.
14. The method of claim 13, further comprising: transferring said solidified composite to a substantially final shape die cavity; heating said substantially final shape die cavity such that said solidified composite therein is at least partially melted; and applying additional pressure to said at least partially melted composite until a final shape of said component defined by said final shape die cavity has substantially solidified.
15. The method of claim 14, wherein said substantially final shape die cavity is shaped to define an automotive engine block.
16. The method of claim 13, further comprising heat treating said component once it has been has substantially solidified.
17. The method of claim 1, wherein said introducing by said semi-solid metal forming comprises: maintaining said composite in a substantially melted form; placing said substantially melted composite into a substantially preliminary shape die cavity; and providing a combination of heat and pressure until said substantially melted composite defined by said preliminary shape die cavity has substantially solidified.
18. The method of claim 17, further comprising: transferring said solidified composite from said preliminary shape die cavity to a substantially final shape die cavity; heating said substantially final shape die cavity such that said solidified composite therein is at least partially melted; and applying additional pressure to said at least partially melted composite until a final shape of said component defined by said final shape die cavity has substantially solidified.
19. A method of making a reinforced metal alloy component, said method comprising: introducing at least one reinforcing phase precursor into a bulk alloy that is selected from the group consisting of high-entropy alloys, aluminum-based alloys, magnesium-based alloys and combinations thereof; catalyzing said reinforcing phase precursor such that a reinforcing phase will grow therefrom; and forming said component as a composite of said bulk alloy and said reinforcing phase using one of squeeze casting and semi-solid metal, said forming comprising: heating said composite until it is in an at least partially melted form; placing said at least partially melted composite into a die cavity; and imparting an elevated pressure on said at least partially melted composite until a shape of said component defined by said die cavity has substantially solidified.
20. The method of claim 19, wherein said bulk alloy is in a substantially solid powder form at the time said at least one reinforcing phase precursor is introduced thereto.
21. The method of claim 19, wherein said bulk alloy is in a substantially melted liquid form at the time said at least one reinforcing phase precursor is introduced thereto.
22. The method of claim 19, wherein said reinforcing phase is selected from the group consisting of ceramics, intermetallics, rare earth elements and dispersoids.
23. A method of making a reinforced metal alloy component, said method comprising: introducing at least one reinforcing phase precursor into a bulk alloy that is selected from the group consisting of high-entropy alloys, aluminum-based alloys, magnesium-based alloys and combinations thereof; and shaping said component as a composite of said bulk alloy and a reinforcing phase that is formed by activation of said reinforcing phase precursor, said shaping selected from the group consisting essentially of squeeze casting and semi-solid metal forming, said shaping comprising: heating said composite until it is in an at least partially melted form; placing said at least partially melted composite into a die cavity; and imparting an elevated pressure on said at least partially melted composite until a shape of said component defined by said die cavity has substantially solidified.
24. The method of claim 23, wherein said activation comprises catalyzing said at least one reinforcing phase precursor by increasing the temperature of said bulk alloy during at least one of said shaping or at least one subsequent heat treating step.
25. The method of claim 24, wherein said activation comprises catalyzing said at least one reinforcing phase precursor by increasing the temperature of said bulk alloy above its solidus temperature during said shaping and increasing the temperature of said reinforced metal alloy component during at least one subsequent heat treating step.
Description
BRIEF DESCRIPTION OF THE DRAWINGS
(1) The following detailed description of the preferred embodiments of the present invention can be best understood when read in conjunction with the following drawings, where like structure is indicated with like reference numerals and in which:
(2)
(3)
(4)
(5)
DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS
(6) Referring first to
(7) Referring next to
(8) As mentioned above, SSM-based microstructures have superior flow characteristics when compared to those with dendritic microstructure, as the equiaxed microstructure of the billet feedstock can be heated to the semi-solid temperature range to convert the fine grained billet microstructure into the globulitic microstructure which allows a relatively free flowing (yet still viscous) fluid behavior. This in turn allows higher metal flow velocities without the attendant turbulence problems, which in turn significantly improves component production rates. In addition to SSM forming producing no turbulence during filling, it also uses a lower incoming metal temperature so that there less thermal shock to the tooling, employs shorter cycle times due to lower incoming metal temperature, and involves no handling of liquid metal, and produces a fine microstructure with low or no porosity and high mechanical properties. Squeeze casting affords similar advantages, including enjoying the benefit of: producing good surface finish (which contributes to reduced post-cast finishing), producing near net shape parts with almost no material waste, permitting on-site melting of any residual material as a way to reduce waste, and leaves the resulting components with fine microstructure, low or no porosity and high mechanical properties.
(9) Referring with particularity to
(10) Referring with particularity to
(11) Regardless of which of the two parallel paths 300A, 300B are used, subsequent steps include transferring the solid preliminarily-shaped part to a final shaped die 350, heating the finally-shaped part and die in order to partially melt the part 360, applying elevated pressure to the partially-melted part 370 in order to help solidify it in a substantially final shape 380, ejecting the solidified part 390 and performing any optional post-ejection heat treatment 400. In one preferred form, the post-ejection heat treatment 400 may help to further develop the desired microstructures, including uniformly distributed reinforcing phases of different sizes ranging from nanometers to micrometers. With appropriate selection of the precursors to seed the nucleation sites, the particles of the reinforcing phase will be higher in elastic modulus than the bulk alloy, thereby providing additional stiffness of the resulting composite part. In a preferred form, the precursor would be soluble in the alloy at a temperature above which the alloy is solid such that a catalyzing activation arising from increases in temperature, pressure or other energy source (such as ultrasound, vibration or electromagnetism) will promote the formation of the nucleation sites so that the reinforcing phase particles will grow at the nucleation sites to micro size because of one or more of structure, size and composition at the site. The resultant reinforcing particles will themselves be insoluble in the alloy at some temperature below the temperature at which they nucleated, and may be in the form of compounds including (but not limited to) ceramics, intermetallics or dispersoids, as well as a combination of them. Such ceramics may include silicon carbide, silicon nitride, silicon oxide, boron carbide, boron nitride, titanium nitride, titanium carbide, titanium oxide, silicon aluminum oxynitride, steatite (magnesium silicates), aluminum oxide (alumina) and zirconium dioxide (zirconia, which can be chemically stabilized in several different forms, or in metastable structures that can impart transformation toughening, such as the less brittle partially stabilized zirconia). Likewise, suitable intermetallics may include FeAl, Fe.sub.3Al, FeAl.sub.3, FeCo, Cu.sub.3Al, NiTi, NiAl, Ni.sub.3Al, Ag.sub.3Sn, Cu.sub.3Sn, TiSi.sub.2, MgCu.sub.2, MgZn.sub.2, MgNi.sub.2, CuZn, Cu.sub.31Sn.sub.8, SbSn as well as others containing three or more elements. Compounds of low cost rare earth elements such as Ce and La may also be used. The precursors that lead to the reinforcing particles can be added separately or together during the process, depending on the need. Significantly, the precursor achieves two things: first, it provides nucleation sites at which the reinforcing phase particles can grow, and second, it provides the elements which will feed the reinforcing phase growth. As such, they may (or may not) be made from a single composition. Moreover, they may be coated (as discussed below) so that the outside composition is different from that of the core that is controlled by the growth of the various reinforcing phases.
(12) In one preferred form, activation that results in forming the reinforcing phases at the nucleation sites includes catalyzing the one or more precursors through increasing the temperature of the bulk alloy above its solidus temperature. Once the precursor has been catalyzed, the resulting reinforcing phase avoids reverting back in the presence of the liquid melt by virtue of their relatively high melting temperatures in conjunction with their nucleation taking place at temperatures around or above the liquidus temperature T.sub.L of common aluminum and magnesium die casting alloys. In fact, these reinforcing phases (preferably in the form of particles) actually can be nucleated over a fairly wide range of temperature (for example, between about 200 to 800 C.), depending on the solution in which the nucleation happens, as well as upon the size of the reinforcing phase. For example, smaller radius particles form at lower melting temperature due to their high surface energy. In situations where use of an aluminum-based material is contemplated, the present inventors believe an activation temperature range of about 500 C. to 800 C. would be sufficient, while an activation temperature range of about 425 C. to 700 C. would be proper for a magnesium-based material. Within the context of the present invention, it is expected that the nucleation to occur around the liquidus temperature T.sub.L of typical casting alloys examples of which are shown in the table below.
(13) TABLE-US-00001 Solidus Temperatures Liquidus Temperatures Alloy C. F. C. F. Al 356.0 557 1035 613 1135 Al 380.0 538 1000 593 1100 Al 2014 507 945 638 1180 Mg AZ91 470 878 595 1100 Mg AM60 545 1010 615 1140
(14) Proper choice of the reinforcing phases will ensure that they remain solid even in the very hot bulk alloy due to their high melting point. For example, the melting temperature of one typical reinforcing oxide particle, titanium dioxide TiO.sub.2, is 1843 C. or 3350 F. As is understood by those skilled in the art, liquidus temperature T.sub.L and solidus temperature Ts such as those depicted in the table above are a function of materials compositions based on phase diagrams. Thus, a good solidus Ts temperature range for aluminum would be between about 500 C. and 700 C., while a desirable liquidus temperature T.sub.L range would be between about 550 C. and 750 C. Likewise, a preferred solidus temperature T.sub.S range for magnesium alloys would be between about 425 C. and 600 C., with a corresponding liquidus temperature T.sub.L range of about 550 C. to 700 C.
(15) Moreover, activation of the precursors through the catalyzation steps discussed herein improves wettability through reduced interfacial energy; this in turn produces improvements in the desired reinforcing phases. Thus, in addition to controlling the size of the reinforcing phase, the precursors can be coated (especially when in ceramic form) with metals that generally have low-melting points, or compound particles by mechanical milling, as well as by mixing them in a solvent and then dried. The solvent or carrier (which may remain or be removed after processing) may be used to improve transformation process efficiency or effectiveness by helping reduce the interfacing energy between the surfaces of particles, as well as to avoid particle clustering. The solvent or carrier can be organic or inorganic chemicals, such as alcohol, chlorinated solvents, or commercially-available industrial solvent, as well as solid lubricant such as boron nitride powder, molybdenum disulfide (MbS.sub.2) powder or the like.
(16) A significant benefit to using squeeze casting or SSM forming with the present composite-generating approach is that nontraditional compositions of aluminum or magnesium casting alloys may be used, including those with significant non-eutectic compositions thatwhile possessing valuable attributes for engine blocks and related automotive componentshave hitherto been avoided due in part to the difficulty in casting such alloys into repeatable, high-quality finished products. Likewise, alloys traditionally associated with forged materials (such as aluminum-copper, aluminum-magnesium (either with or without additional alloying ingredients) may be used with the present invention, thereby opening up the range of usable materials to ones deemed hitherto inappropriate for low-cost, high-volume component manufacture. By way of example, the hypereutectic Alloy 390 is traditionally difficult to use because of the inability to maintain a desirable microstructure as a way to control the size and distribution of primary silicon during the casting process. By reducing the influence of the high heat of fusion associated with formation of primary silicon, the combination of squeeze casting or liquid forging with the in-situ composite formation discussed herein avoids traditional long cycle times and concomitant shortened tool life that previously limited the applicability of this (as well as other) alloys. The possibility of using hard-to-cast alloys (such as from the Al/Cu class of alloys) is especially desirable in the formation of engine block 100 in that the cylinder bores defined therein may be produced in a bare-bore configuration where no separate iron-based cylinder liners or other inserts would be needed. Moreover, traditional hypoeutectic alloys (such as Alloys 319 and 356, each with roughly 6 to 7 percent Si) that the Assignee of the present disclosure currently uses for engine blocks, as well as near-eutectic alloys (such as Alloy 380, with roughly 9% Si) may be beneficially used with the methods disclosed herein.
(17) It is noted that terms like preferably, commonly, and typically are not utilized herein to limit the scope of the claimed invention or to imply that certain features are critical, essential, or even important to the structure or function of the claimed invention. Rather, these terms are merely intended to highlight alternative or additional features that may or may not be utilized in a particular embodiment of the present invention. Moreover, the term substantially is utilized herein to represent the inherent degree of uncertainty that may be attributed to any quantitative comparison, value, measurement, or other representation. As such, it may represent the degree by which a quantitative representation may vary from a stated reference without resulting in a change in the basic function of the subject matter at issue.
(18) Having described the invention in detail and by reference to specific embodiments thereof, it will be apparent that modifications and variations are possible without departing from the scope of the invention defined in the appended claims. More specifically, although some aspects of the present invention are identified herein as preferred or particularly advantageous, it is contemplated that the present invention is not necessarily limited to these preferred aspects of the invention.