MAGNESIUM ALLOY AND METHOD FOR PRODUCING SAME
20260125780 ยท 2026-05-07
Inventors
- Yoshihito KAWAMURA (Chuo-ku, Kumamoto-shi Kumamoto, JP)
- Shinichi INOUE (Chuo-ku, Kumamoto-shi Kumamoto, JP)
Cpc classification
C22C23/04
CHEMISTRY; METALLURGY
B22D21/007
PERFORMING OPERATIONS; TRANSPORTING
International classification
C22C23/04
CHEMISTRY; METALLURGY
B22D21/00
PERFORMING OPERATIONS; TRANSPORTING
Abstract
Provided is a magnesium alloy having high strength and high thermal conductivity containing a atom % of Zn and b atom % of Y, a remainder consisting of Mg and unavoidable impurities, where a and b satisfy formulas 1 to 8. The magnesium alloy contains an Mg.sub.3Zn.sub.3Y.sub.2 phase or both an Mg.sub.3Zn.sub.3Y.sub.2 phase and an Mg.sub.3Zn.sub.6Y phase and does not contain a long period stacking ordered phase. (Formula 1) a=0.5 (0.25b1.2) (Formula 2) b=1.2 (0.5a1.62) (Formula 3) a=1.35b (1.2b3) (Formula 4) b=3 (4.05a7) (Formula 5) a=7 (0.25b3) (Formula 6) b=0.25 (0.5a7) (Formula 7) a=4.2b+0.7 (0.25b1.5) (Formula 8) b=0.25 (0.5a1.75).
Claims
1. A magnesium alloy comprising: a atom % of Zn; b atom % of Y; and a remainder consisting of Mg and unavoidable impurities, wherein a Zn content of the a atom % and a Y content of the b atom % are set in a range enclosed by straight lines represented by the following (1) to (8) according to coordinates (b, a) where a is taken on a vertical axis and b is taken on a horizontal axis, the magnesium alloy contains a Mg.sub.3Zn.sub.3Y.sub.2 phase or both a Mg.sub.3Zn.sub.3Y.sub.2 phase and a Mg.sub.3Zn.sub.6Y phase, and the magnesium alloy does not contain a long period stacking ordered structure phase. (1) When b is in a range defined by the following Formula 1a, a straight line represented by the following Formula 1b is obtained.
2. The magnesium alloy according to claim 1, wherein the magnesium alloy has a thermal conductivity of 90 W/m.Math.K or more.
3. The magnesium alloy according to claim 1, wherein the magnesium alloy contains any one element selected from the group consisting of Yb in an amount of 0.05 atom % or more and 0.6 atom % or less, Be in an amount of 0.03 atom % or more and 0.3 atom % or less, Ca in an amount of 1.0 atom % or more and 2.0 atom % or less, and Sr in an amount of 0.1 atom % or more and 2.0 atom % or less.
4. The magnesium alloy according to claim 1, wherein Zn/Y, which is a composition ratio of Zn to Y in the magnesium alloy, is in a range of 2 or more and 5 or less.
5. The magnesium alloy according to claim 1, wherein the magnesium alloy has a structure in which the Mg.sub.3Zn.sub.3Y.sub.2 phase is not formed in a network shape at grain boundaries or a structure in which both the Mg.sub.3Zn.sub.3Y.sub.2 phase and the Mg.sub.3Zn.sub.6Y phase are not formed in a network shape at grain boundaries.
6. The magnesium alloy according to claim 1, wherein the magnesium alloy has a yield strength of 300 MPa or more and an elongation of 5% or more.
7. A method for manufacturing a magnesium alloy containing an a atom % of Zn, a b atom % of Y, and a remainder consisting of Mg and unavoidable impurities, the method comprising: a step (a) of forming a cast material by casting the magnesium alloy at a solidification rate of less than 1000 K/sec, wherein a Zn content of a atom % and a Y content of b atom % are set in a range enclosed by straight lines represented by the following (1) to (8) according to coordinates (b, a) where a is taken on a vertical axis and b is taken on a horizontal axis, the cast material contains a Mg.sub.3Zn.sub.3Y.sub.2 phase or both a Mg.sub.3Zn.sub.3Y.sub.2 phase and a Mg.sub.3Zn.sub.6Y phase, and the cast material does not contain a long period stacking ordered structure phase. (1) When b is in a range defined by the following Formula 1a, a straight line represented by the following Formula 1b is obtained.
8. The method for manufacturing a magnesium alloy according to claim 7, further comprising: a step (b) of forming a heat-treated material by performing heat treatment on the cast material after the step (a), wherein the heat-treated material has a thermal conductivity of 90 W/m K or more, the heat-treated material contains the Mg.sub.3Zn.sub.3Y.sub.2 phase or both the Mg.sub.3Zn.sub.3Y.sub.2 phase and the Mg.sub.3Zn.sub.6Y phase, and the heat-treated material does not contain the long period stacking ordered structure phase.
9. The method for manufacturing a magnesium alloy according to claim 8, wherein conditions for performing the heat treatment are set to at a temperature of 200 C. or more and 500 C. or less and a heat treatment time of 48 hours or less.
10. The magnesium alloy according to claim 7, wherein the magnesium alloy contains any one element selected from the group consisting of Yb in an amount of 0.05 atom % or more and 0.6 atom % or less, Be in an amount of 0.03 atom % or more and 0.3 atom % or less, Ca in an amount of 1.0 atom % or more and 2.0 atom % or less, and Sr in an amount of 0.1 atom % or more and 2.0 atom % or less.
11. The method for manufacturing a magnesium alloy according to any one of claim 7, wherein Zn/Y, which is a composition ratio of Zn to Y in the cast material, is in a range of 2 or more and 5 or less.
12. The method for manufacturing a magnesium alloy according to claim 8, further comprising: a step (c) of forming a plastically processed material by performing plastic processing on the heat-treated material after the step (a) or the step (b), wherein the plastically processed material has a structure in which the Mg.sub.3Zn.sub.3Y.sub.2 phase is not formed in a network shape at grain boundaries or a structure in which both the Mg.sub.3Zn.sub.3Y.sub.2 phase and the Mg.sub.3Zn.sub.6Y phase are not formed in a network shape at grain boundaries.
13. The method for manufacturing a magnesium alloy according to claim 12, wherein the plastically processed material has a yield strength of 300 MPa or more and an elongation of 5% or more.
Description
BRIEF DESCRIPTION OF THE DRAWINGS
[0042]
[0043]
[0044]
[0045]
[0046]
[0047]
DETAILED DESCRIPTION OF THE EMBODIMENTS
[0048] Hereinafter, embodiments of the invention will be described in detail with reference to the drawings. However, the invention is not limited to the following description, and it will be easily understood by those skilled in the art that the modes and details of the invention can be modified in various forms without departing from the concept and scope of the invention.
[0049] Therefore, the invention should not be interpreted as being limited to the contents of the embodiments shown below.
First Embodiment
<Composition of Magnesium Alloy>
[0050]
[0051] In addition, it is preferable that the magnesium alloys according to one aspect of the invention have a thermal conductivity of 90 W/m.Math.K or more (preferably 100 W/m.Math.K or more, more preferably 110 W/m.Math.K or more, and still more preferably 130 W/m.Math.K or more).
[0052] In addition, in this specification, the cast materials refer to cast materials that are cast at a solidification rate of less than 1000 K/s, and includes cast materials produced by casting methods such as metal mold casting, sand casting, and semi-continuous casting, as well as die casting, injection molding, and twin-roll casting.
[0053] In addition, in this specification, the heat-treated cast materials refer to heat-treated materials obtained by heat-treating the above-described cast materials.
[0054] In addition, in this specification, the plastically processed cast materials include both plastically processed materials produced by subjecting the above-described heat-treated materials to plastic processing such as extrusion, rolling, forging, wire drawing, and the solidification and molding of chipping material, and plastically processed materials produced by subjecting the above-described cast materials to plastic processing such as extrusion, rolling, forging, wire drawing, and the solidification and molding of chipping material without performing heat treatment on the above-described cast materials.
[0055] The magnesium alloys according to the present embodiment have the following composition range. The magnesium alloys contain a atom % of Zn, b atom % of Y, and a remainder consisting of Mg and unavoidable impurities.
[0056] As shown in
[0057] (1) When b is in a range defined by the following Formula 1a, a straight line represented by the following Formula 1b is obtained.
[0058] (2) When b is in a range defined by the following Formula 2a, a straight line represented by the following Formula 2b is obtained.
[0059] (3) When a is in a range defined by the following Formula 3a, a straight line represented by the following Formula 3b is obtained.
[0060] (4) When b is in a range defined by the following Formula 4a, a straight line represented by the following Formula 4b is obtained.
[0061] (5) When a is in a range defined by the following Formula 5a, a straight line represented by the following Formula 5b is obtained.
[0062] (6) When b is in a range defined by the following Formula 6a, a straight line represented by the following Formula 6b is obtained.
[0063] (7) When b is in a range defined by the following Formula 7a, a straight line represented by the following Formula 7b is obtained.
[0064] (8) When a is in a range defined by the following Formula 8a, a straight line represented by the following Formula 8b is obtained.
<Constituent Phases of Magnesium Alloy>
[0065] As shown in
[0066] As shown in
[0067] By subjecting each of the cast materials and the heat-treated cast materials of the magnesium alloys shown in
[0068] By performing plastic processing such as extrusion on the MgZnY alloy having high thermal conductivity shown in
[0069] According to the present embodiment, by setting the composition range of Zn and Y, which have a large negative mixing enthalpy, to the range shown in
[0070]
[0071] According to
[0072] In addition, the reason that the lower limit of Ca to be added is set to 1.0 atom % is that a CaO film starts to form on the outermost layer when the amount of Ca added is equal to or greater than this amount, and the reason that the upper limit of Ca is set to 2.0 atom % is to suppress adverse effects on mechanical properties.
[0073] In addition, in addition to Yb and Ca, it can be expected that the above-described magnesium alloys can also be made non-flammable by adding Be in an amount of 0.03 atom % or more and 0.3 atom % or less or Sr in an amount of 0.1 atom % or more and 2.0 atom % or less to the magnesium alloys.
[0074] The reason that non-flammability can also be achieved by adding Be is that it has been reported that the ignition temperature of an alloy containing Y is improved. The reason that the lower limit of Be is set to 0.03 atom % is that this concentration improves the oxygen barrier performance of the Y.sub.2O.sub.3 film, and the reason that the upper limit of Be is set to 0.3 atom % is that the ignition temperature is not improved at this concentration or higher.
[0075] The reason that non-flammability can also be achieved by adding Sr is that it has been reported that the ignition temperature of an alloy containing Y is improved. The reason that the lower limit of Sr is set to 0.1 atom % is that this concentration improves the oxygen barrier performance of the Y.sub.2O.sub.3 film, and the reason that the upper limit of Sr is set to 2.0 atom % is to prevent an increase in the volume fraction of intermetallic compounds.
[0076]
[0077] As shown in
Second Embodiment
<Method for Manufacturing Magnesium Alloy>
[0078] A magnesium alloy having the composition range according to the first embodiment is melted at a predetermined temperature in a non-flammable gas atmosphere (for example, in an Ar atmosphere), and then is cast at a solidification rate of less than 1000 K/s.
[0079] The magnesium alloy ingot after casting is cut into a predetermined shape. Accordingly, a cast material is produced. The cast material contains the Mg.sub.3Zn.sub.3Y.sub.2 phase or both the Mg.sub.3Zn.sub.3Y.sub.2 phase and the Mg.sub.3Zn.sub.6Y phase, and does not contain the long period stacking ordered structure phase.
[0080] Next, a heat-treated cast material is formed by performing heat treatment on the cast material at a temperature of 200 C. or more and 450 C. or less (preferably 300 C. or more and 450 C. or less) for 0 hour or more and 48 hours or less. The heat-treated cast material has a thermal conductivity of 90 W/m.Math.K or more (preferably 100 W/m.Math.K or more, more preferably 110 W/m.Math.K or more, and still more preferably 130 W/m.Math.K or more). In addition, the heat-treated cast material contains the Mg.sub.3Zn.sub.3Y.sub.2 phase or both the Mg.sub.3Zn.sub.3Y.sub.2 phase and the Mg.sub.3Zn.sub.6Y phase, and does not contain the long period stacking ordered structure phase. Incidentally, the above-described heat treatment may be performed in an air atmosphere.
[0081] Next, plastic processing is performed on the heat-treated cast material. The plastic processing includes extrusion, rolling, forging, wire drawing, severe plastic deformation, and the like. The severe plastic deformation includes equal-channel-angular-extrusion (ECAE) processing.
[0082] The plastically processed material on which the above-described plastic processing has been performed has a structure in which the Mg.sub.3Zn.sub.3Y.sub.2 phase is not formed in a network shape at grain boundaries (a structure in which a network is formed in a collapsed state) or a structure in which both the Mg.sub.3Zn.sub.3Y.sub.2 phase and the Mg.sub.3Zn.sub.6Y phase are not formed in a network shape at grain boundaries (a structure in which a network is formed in a collapsed state). In addition, the plastically processed material has a yield strength of 300 MPa or more and an elongation of 5% or more.
[0083] Incidentally, in the present embodiment, plastic processing is performed on the heat-treated cast material; however, plastic processing may be performed on the above-described cast material.
[0084] In addition, it is preferable that the plastically processed materials obtained by performing plastic processing on each of the cast material and the heat-treated cast material described above contain the Mg.sub.3Zn.sub.3Y.sub.2 phase or both the Mg.sub.3Zn.sub.3Y.sub.2 phase and the Mg.sub.3Zn.sub.6Y phase, and do not contain the long period stacking ordered structure phase.
[0085] In addition, each of the cast material and the plastically processed materials described above also has high thermal conductivity.
<Casting Chip Solidification>
[0086] A cast material is produced using the same method as the above-described casting method. Next, for example, a chip material chipped into a size of 1 to 2 mm is formed by cutting the cast material using a machine. Next, a solidified molded material is formed by solidifying and molding the chip material at room temperature through pressure molding.
[0087] In addition, before the chip material is formed, the same heat treatment as that of the above-described casting method may be performed on the cast material. In addition, before the solidified molded material is formed, the same heat treatment as that of the above-described casting method may be performed on the chip material. In addition, the same heat treatment as that of the above-described casting method may be formed on the solidified molded material. The solidified molded material after the heat treatments has a thermal conductivity of 90 W/K.Math.m or more (preferably 100 W/m.Math.K or more, more preferably 110 W/m.Math.K or more, and still more preferably 130 W/m.Math.K or more).
[0088] In addition, each of the chip material, the heat-treated chip material on which heat treatment has been performed, the heat-treated material obtained by performing heat treatment on the chip material, and the solidified molded material described above contains the Mg.sub.3Zn.sub.3Y.sub.2 phase or both the Mg.sub.3Zn.sub.3Y.sub.2 phase and the Mg.sub.3Zn.sub.6Y phase, and does not contain the long period stacking ordered structure phase.
[0089] Incidentally, plastic processing may be performed on the solidified molded material. Accordingly, a plastically processed material having a yield strength of 300 MPa or more and an elongation of 5% or more.
<Injection Molding Method>
[0090] An injection-molded material is produced by heating and melting a magnesium alloy having the composition range according to the first embodiment at a predetermined temperature in a non-flammable gas atmosphere (for example, in an Ar atmosphere), and injecting the molten magnesium alloy melt into a mold and cooling and solidifying the molten magnesium alloy melt. It is preferable that the cooling rate is 1000 K/sec or less.
[0091] Next, a heat-treated injection-molded material is formed by performing the same heat treatment as that of the above-described casting method on the above-described injection-molded material. It is preferable that the heat-treated injection-molded material has a thermal conductivity of 90 W/m.Math.K or more (preferably 100 W/m.Math.K or more, more preferably 110 W/m.Math.K or more, and still more preferably 130 W/m.Math.K or more).
[0092] In addition, each of the injection-molded material and the heat-treated injection-molded material described above contains the Mg.sub.3Zn.sub.3Y.sub.2 phase or both the Mg.sub.3Zn.sub.3Y.sub.2 phase and the Mg.sub.3Zn.sub.6Y phase, and does not contain the long period stacking ordered structure phase.
<Die Casting Method>
[0093] A die-cast material is produced by heating and melting a magnesium alloy having the composition range according to the first embodiment at a predetermined temperature in a non-flammable gas atmosphere (for example, in an Ar atmosphere), and pressure-feeding the molten magnesium alloy melt into a mold. It is preferable that the cooling rate at this time is less than 1000 K/sec. Incidentally, the die casting method is a casting method for mass-producing castings with high dimensional accuracy in a short period of time.
[0094] Next, a heat-treated die-cast material is formed by performing the same heat treatment as that of the above-described casting method on the above-described die-cast material. It is preferable that the heat-treated die-cast material has a thermal conductivity of 90 W/m.Math.K or more (preferably 100 W/m.Math.K or more, more preferably 110 W/m.Math.K or more, and still more preferably 130 W/m.Math.K or more).
[0095] In addition, each of the die-cast material and the heat-treated die-cast material described above contains the Mg.sub.3Zn.sub.3Y.sub.2 phase or both the Mg.sub.3Zn.sub.3Y.sub.2 phase and the Mg.sub.3Zn.sub.6Y phase, and does not contain the long period stacking ordered structure phase.
EXAMPLE
[0096]
[0097] The W phase shown in
[0098] According to
[0099] Cast ingots were produced by weighing raw materials for the samples having the compositions shown in
[0100] The samples are processed into 5 mm1-3 mm or 551-3 mm.sup.3. After the dimensions and weights of the samples are measured, blackening treatment is performed on the surfaces of the samples using a dry carbon spray. After the blackening treatment, weight measurement is performed again, and then the thermal diffusivity of the samples is measured using the laser flash method. The product of the obtained thermal diffusivity, the specific gravity, and the specific heat capacity of the samples is the thermal conductivity.
[0101] Next, heat-treated cast materials were formed by performing heat treatment on the above-described cast materials of the samples at a temperature of 360 C. for 15 hours. The results of measuring the thermal conductivity of these heat-treated cast materials are shown in
[0102] Next, extrusion materials were formed by performing extrusion on the heat-treated cast materials. The extrusion conditions at this time were set to an extrusion ratio of 15, an extrusion temperature of 250 C., and an extrusion rate of 1.0 mm/s. The extrusion materials can realize excellent yield stress and ductility while maintaining high thermal conductivity.
[0103]
[0104]
[0105]
[0106]
[0107] According to