CN112453403A - Preparation method of low-cost powder metallurgy aluminum lithium alloy - Google Patents
Preparation method of low-cost powder metallurgy aluminum lithium alloy Download PDFInfo
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- 229910001148 Al-Li alloy Inorganic materials 0.000 title claims abstract description 38
- JFBZPFYRPYOZCQ-UHFFFAOYSA-N [Li].[Al] Chemical compound [Li].[Al] JFBZPFYRPYOZCQ-UHFFFAOYSA-N 0.000 title claims abstract description 38
- 239000001989 lithium alloy Substances 0.000 title claims abstract description 37
- 238000004663 powder metallurgy Methods 0.000 title claims abstract description 25
- 238000002360 preparation method Methods 0.000 title claims abstract description 9
- WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 claims abstract description 27
- 229910052744 lithium Inorganic materials 0.000 claims abstract description 27
- 239000000843 powder Substances 0.000 claims abstract description 25
- WMFOQBRAJBCJND-UHFFFAOYSA-M Lithium hydroxide Chemical compound [Li+].[OH-] WMFOQBRAJBCJND-UHFFFAOYSA-M 0.000 claims abstract description 21
- 238000000034 method Methods 0.000 claims abstract description 18
- KWGKDLIKAYFUFQ-UHFFFAOYSA-M lithium chloride Chemical compound [Li+].[Cl-] KWGKDLIKAYFUFQ-UHFFFAOYSA-M 0.000 claims abstract description 16
- FUJCRWPEOMXPAD-UHFFFAOYSA-N lithium oxide Chemical compound [Li+].[Li+].[O-2] FUJCRWPEOMXPAD-UHFFFAOYSA-N 0.000 claims abstract description 9
- 229910001947 lithium oxide Inorganic materials 0.000 claims abstract description 9
- XGZVUEUWXADBQD-UHFFFAOYSA-L lithium carbonate Chemical compound [Li+].[Li+].[O-]C([O-])=O XGZVUEUWXADBQD-UHFFFAOYSA-L 0.000 claims abstract description 8
- 229910052808 lithium carbonate Inorganic materials 0.000 claims abstract description 6
- 238000000498 ball milling Methods 0.000 claims description 26
- 238000005245 sintering Methods 0.000 claims description 21
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 14
- 239000011812 mixed powder Substances 0.000 claims description 14
- XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 claims description 12
- 150000001875 compounds Chemical class 0.000 claims description 11
- 229910045601 alloy Inorganic materials 0.000 claims description 9
- 239000000956 alloy Substances 0.000 claims description 9
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 claims description 9
- 239000000463 material Substances 0.000 claims description 9
- 238000002156 mixing Methods 0.000 claims description 9
- MCMNRKCIXSYSNV-UHFFFAOYSA-N Zirconium dioxide Chemical compound O=[Zr]=O MCMNRKCIXSYSNV-UHFFFAOYSA-N 0.000 claims description 8
- 238000001192 hot extrusion Methods 0.000 claims description 8
- 229910052757 nitrogen Inorganic materials 0.000 claims description 7
- 238000003825 pressing Methods 0.000 claims description 7
- 229910052786 argon Inorganic materials 0.000 claims description 6
- 238000000227 grinding Methods 0.000 claims description 6
- HBBGRARXTFLTSG-UHFFFAOYSA-N Lithium ion Chemical compound [Li+] HBBGRARXTFLTSG-UHFFFAOYSA-N 0.000 claims description 5
- 229910052593 corundum Inorganic materials 0.000 claims description 4
- 239000010431 corundum Substances 0.000 claims description 4
- 238000001035 drying Methods 0.000 claims description 4
- 229910052580 B4C Inorganic materials 0.000 claims description 3
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims description 3
- INAHAJYZKVIDIZ-UHFFFAOYSA-N boron carbide Chemical compound B12B3B4C32B41 INAHAJYZKVIDIZ-UHFFFAOYSA-N 0.000 claims description 3
- 238000000465 moulding Methods 0.000 claims description 3
- 238000004321 preservation Methods 0.000 claims description 3
- HBMJWWWQQXIZIP-UHFFFAOYSA-N silicon carbide Chemical compound [Si+]#[C-] HBMJWWWQQXIZIP-UHFFFAOYSA-N 0.000 claims description 3
- 229910010271 silicon carbide Inorganic materials 0.000 claims description 3
- 238000009694 cold isostatic pressing Methods 0.000 claims description 2
- 238000000280 densification Methods 0.000 claims description 2
- 230000001681 protective effect Effects 0.000 claims description 2
- 238000005303 weighing Methods 0.000 claims description 2
- 238000004519 manufacturing process Methods 0.000 abstract description 4
- 230000000694 effects Effects 0.000 abstract description 2
- 238000003860 storage Methods 0.000 abstract description 2
- 239000013585 weight reducing agent Substances 0.000 abstract 1
- 238000003466 welding Methods 0.000 abstract 1
- 230000006835 compression Effects 0.000 description 5
- 238000007906 compression Methods 0.000 description 5
- 238000000748 compression moulding Methods 0.000 description 5
- 238000010438 heat treatment Methods 0.000 description 5
- 238000005728 strengthening Methods 0.000 description 5
- 229910000838 Al alloy Inorganic materials 0.000 description 4
- 229910052782 aluminium Inorganic materials 0.000 description 4
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 4
- 238000001125 extrusion Methods 0.000 description 4
- 239000000126 substance Substances 0.000 description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
- 238000001816 cooling Methods 0.000 description 3
- 239000006185 dispersion Substances 0.000 description 3
- 239000011159 matrix material Substances 0.000 description 3
- 238000005266 casting Methods 0.000 description 2
- 230000001276 controlling effect Effects 0.000 description 2
- 239000013078 crystal Substances 0.000 description 2
- 229910001868 water Inorganic materials 0.000 description 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
- 229910000861 Mg alloy Inorganic materials 0.000 description 1
- 229910000676 Si alloy Inorganic materials 0.000 description 1
- 238000003723 Smelting Methods 0.000 description 1
- CSDREXVUYHZDNP-UHFFFAOYSA-N alumanylidynesilicon Chemical compound [Al].[Si] CSDREXVUYHZDNP-UHFFFAOYSA-N 0.000 description 1
- SNAAJJQQZSMGQD-UHFFFAOYSA-N aluminum magnesium Chemical compound [Mg].[Al] SNAAJJQQZSMGQD-UHFFFAOYSA-N 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 230000007797 corrosion Effects 0.000 description 1
- 238000005260 corrosion Methods 0.000 description 1
- 230000007547 defect Effects 0.000 description 1
- 238000004880 explosion Methods 0.000 description 1
- 239000000446 fuel Substances 0.000 description 1
- 230000004927 fusion Effects 0.000 description 1
- 239000012535 impurity Substances 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 230000005012 migration Effects 0.000 description 1
- 238000013508 migration Methods 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- RVTZCBVAJQQJTK-UHFFFAOYSA-N oxygen(2-);zirconium(4+) Chemical compound [O-2].[O-2].[Zr+4] RVTZCBVAJQQJTK-UHFFFAOYSA-N 0.000 description 1
- JTJMJGYZQZDUJJ-UHFFFAOYSA-N phencyclidine Chemical compound C1CCCCN1C1(C=2C=CC=CC=2)CCCCC1 JTJMJGYZQZDUJJ-UHFFFAOYSA-N 0.000 description 1
- 239000011148 porous material Substances 0.000 description 1
- 230000001105 regulatory effect Effects 0.000 description 1
- 239000002760 rocket fuel Substances 0.000 description 1
- 230000035900 sweating Effects 0.000 description 1
- 229910001928 zirconium oxide Inorganic materials 0.000 description 1
Classifications
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- 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
- B22F3/00—Manufacture of workpieces or articles from metallic powder characterised by the manner of compacting or sintering; Apparatus specially adapted therefor ; Presses and furnaces
- B22F3/12—Both compacting and sintering
- B22F3/16—Both compacting and sintering in successive or repeated steps
-
- 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
- B22F3/00—Manufacture of workpieces or articles from metallic powder characterised by the manner of compacting or sintering; Apparatus specially adapted therefor ; Presses and furnaces
- B22F3/20—Manufacture of workpieces or articles from metallic powder characterised by the manner of compacting or sintering; Apparatus specially adapted therefor ; Presses and furnaces by extruding
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C1/00—Making non-ferrous alloys
- C22C1/04—Making non-ferrous alloys by powder metallurgy
- C22C1/0408—Light metal alloys
- C22C1/0416—Aluminium-based alloys
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C1/00—Making non-ferrous alloys
- C22C1/04—Making non-ferrous alloys by powder metallurgy
- C22C1/05—Mixtures of metal powder with non-metallic powder
- C22C1/051—Making hard metals based on borides, carbides, nitrides, oxides or silicides; Preparation of the powder mixture used as the starting material therefor
- C22C1/053—Making hard metals based on borides, carbides, nitrides, oxides or silicides; Preparation of the powder mixture used as the starting material therefor with in situ formation of hard compounds
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C21/00—Alloys based on aluminium
-
- 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
- B22F3/00—Manufacture of workpieces or articles from metallic powder characterised by the manner of compacting or sintering; Apparatus specially adapted therefor ; Presses and furnaces
- B22F3/20—Manufacture of workpieces or articles from metallic powder characterised by the manner of compacting or sintering; Apparatus specially adapted therefor ; Presses and furnaces by extruding
- B22F2003/208—Warm or hot extruding
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- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Mechanical Engineering (AREA)
- Materials Engineering (AREA)
- Metallurgy (AREA)
- Organic Chemistry (AREA)
- Manufacturing & Machinery (AREA)
- Powder Metallurgy (AREA)
Abstract
本发明提供了一种低成本粉末冶金铝锂合金的制备方法，属于粉末冶金技术领域。本发明选择氢氧化锂、碳酸锂、氯化锂、氧化锂中的一种或几种作为锂源配制铝锂合金粉末，锂源容易获得，成本低廉。将配制好的粉末经过成形、烧结、挤压等工序得到粉末冶金铝锂合金。与传统熔铸铝锂合金相比，该方法制造成本低廉，锂源选择范围广泛，更易保存与制备，产业化前景良好。获得的粉末冶金铝锂合金密度低，具有良好的减重效果，室温/高温性能和焊接性能优异，在航空航天等领域具有极为广阔的应用前景。The invention provides a preparation method of low-cost powder metallurgy aluminum-lithium alloy, which belongs to the technical field of powder metallurgy. The present invention selects one or more of lithium hydroxide, lithium carbonate, lithium chloride and lithium oxide as the lithium source to prepare the aluminum-lithium alloy powder, the lithium source is easy to obtain and the cost is low. The prepared powder is formed, sintered, extruded and other processes to obtain powder metallurgy aluminum-lithium alloy. Compared with the traditional cast aluminum-lithium alloy, the method has the advantages of low manufacturing cost, wide selection of lithium sources, easier storage and preparation, and good industrialization prospects. The obtained powder metallurgy aluminum-lithium alloy has low density, good weight reduction effect, excellent room temperature/high temperature performance and welding performance, and has extremely broad application prospects in aerospace and other fields.
Description
Technical Field
The invention relates to a preparation method of a low-cost powder metallurgy aluminum lithium alloy, belonging to the technical field of powder metallurgy.
Technical Field
In the aerospace field, the light weight of key components (such as rocket fuel tanks) can not only reduce fuel cost, but also reduce carbon emission and improve carrying capacity. The lithium is used as the lightest metal element, the density of the alloy can be reduced by 3% and the elastic modulus can be increased by 6% when 1% of lithium is added into the aluminum alloy, and compared with the traditional aluminum alloy, the aluminum-lithium alloy has the advantages of low density, high specific strength, high specific rigidity, high fracture toughness, good corrosion resistance and the like, so that the aluminum-lithium alloy has a great application prospect in the field of aerospace.
At present, the method for preparing the aluminum lithium alloy internationally is a fusion casting method. However, lithium is very active in property, and is very easy to react with oxygen, nitrogen, water and the like, a lithium simple substance or an aluminum lithium intermediate alloy is generally added in the smelting process, so that lithium loss is very easy to cause by burning loss, the plasticity of the cast aluminum lithium alloy is poor, the processing yield is low, and the production cost of the conventional cast aluminum lithium alloy is high.
Disclosure of Invention
The invention aims to provide a preparation method of a low-cost powder metallurgy aluminum lithium alloy, which solves the problem of high cost of the aluminum lithium alloy prepared by the traditional casting method.
The technical scheme of the invention is as follows: lithium source compounds such as lithium oxide, lithium carbonate, lithium chloride and lithium oxide are dried in vacuum to remove moisture impurities, so that residual water vapor is prevented from hindering the sintering process. And then ball-milling and mixing the dried lithium source compound powder with pure aluminum powder, alloy element powder or alloy powder, and carrying out the working procedures of forming, sintering, extruding and the like on the prepared mixed powder to obtain the powdery aluminum-lithium alloy. During sintering, the compound of aluminum and lithium reacts to generate lithium and uniformly distributed dispersed phase, and the excellent performance of the aluminum-lithium alloy is obtained through the functions of powder metallurgy fine grain strengthening and dispersion strengthening.
In order to realize the technical scheme of the invention, the specific process steps comprise the following contents:
a) preparing mixed powder: weighing one or more of pure aluminum powder, alloy element powder or alloy powder and a lithium source compound according to required components, and preparing mixed powder by ball milling, wherein the mass fraction of lithium element in the mixed powder is 0.5-5 wt.%.
b) Molding: and (3) performing compression molding on the mixed aluminum lithium alloy powder by adopting one or two of cold isostatic pressing or mould pressing, wherein the compression pressure is 100-500MPa, and the pressure maintaining time is 30-300 s.
c) And (3) sintering: sintering densification is carried out in the protective atmosphere of vacuum, nitrogen or argon, the sintering temperature is 500-630 ℃, and the heat preservation time is 1-10h, so as to obtain the compact powder metallurgy aluminum lithium alloy sintering blank.
d) Deformation processing: and carrying out hot extrusion on the sintered billet at the temperature of 300-500 ℃ to obtain the low-cost powder metallurgy aluminum-lithium alloy with excellent performance.
Preferably, the lithium source compound in step 1) is one or more of lithium hydroxide, lithium carbonate, lithium chloride and lithium oxide.
Preferably, the lithium source compound of step 1) is dried in vacuum before mixing, the drying temperature is 80-170 ℃, and the drying time is 1-5 h.
Preferably, the mixed powder is prepared by ball milling in the step 1), the ball milling tank and the grinding balls are made of one or more of corundum, agate, zirconia, silicon carbide and boron carbide, and the ball milling environment is vacuum (the vacuum degree is 10)-1-10-2Pa), high-purity nitrogen and high-purity argon, wherein the ball-material ratio is 1:1-10:1, and the ball milling time is 1-10 h.
The technical key points of the invention are as follows:
1. lithium hydroxide, lithium carbonate, lithium chloride and lithium oxide which are low in price, wide in source and stable in property are used as lithium sources, and the problems that in the traditional process, a lithium simple substance is easy to oxidize, is difficult to store and is high in manufacturing cost are solved.
2. The lithium source compound is dried in vacuum before mixing, so that the moisture in the lithium source compound can be more fully volatilized, on one hand, the pressure in a ball-milling tank is increased due to the volatilization of water vapor caused by the heating of ball-milling mixing, and the explosion risk exists when the tank is opened; on the other hand, the water can increase the molding difficulty of the mixed powder, so that the strength of a molded green body is reduced, and the green body is easy to delaminate and lack edges.
3. By controlling the sintering temperature and the heat preservation time, the powder metallurgy aluminum lithium alloy sintering blank generates dispersed phase alumina in the preparation process, and the dispersed phase alumina is uniformly distributed in an aluminum matrix to play a role in dispersion strengthening. If the temperature during sintering is too low, dispersed phase alumina cannot be generated and cannot be uniformly distributed in the aluminum matrix. If the sintering temperature is too high, low-melting-point components (such as lithium) in the alloy can generate substance migration from defects such as crystal boundary, holes and the like, the crystal boundary phase is separated out and excessively grows, so that the mechanical property and the processing property of the material are seriously deteriorated, the phenomenon of sweating can be generated at the same time, the burning loss of lithium elements is serious, the utilization rate of a lithium source is reduced, and the cost is increased.
4. The sintered billet is subjected to hot extrusion at the temperature of 300-500 ℃, and the hot extrusion plays a role in regulating and controlling the formability, so that on one hand, residual pores in the sintered billet are further eliminated, the relative density of the material reaches 100 percent, and the toughness of the material is improved; on the other hand, the powder metallurgy aluminum lithium alloy with the required specification is obtained.
Compared with the prior art, the invention has the following advantages:
(1) the invention adopts lithium hydroxide, lithium carbonate, lithium chloride and lithium oxide as lithium sources, is easy to prepare, store and transport, solves the problems of easy oxidation, difficult storage and higher manufacturing cost of lithium simple substances in the traditional process, and is easy to realize industrialization.
(2) The dispersed phase alumina is generated in the preparation process, is uniformly distributed in an aluminum matrix, plays a role in dispersion strengthening, and has more excellent performance due to the powder metallurgy fine grain strengthening effect.
Detailed Description
Example 1
The lithium hydroxide powder was dried by heating under vacuum at 150 ℃ for 2 h. Ball milling and mixing 2020 aluminum alloy powder and dried lithium hydroxide powder to obtain lithiumThe mass fraction of the elements in the mixed powder was 1 wt.%. The corundum ball milling tank and the agate grinding balls are adopted at the vacuum degree of 10-1Ball milling is carried out in a Pa environment, the ball-material ratio is 1:1, and the ball milling time is 1 h. And (3) performing compression molding on the mixed aluminum lithium alloy powder by adopting isostatic cool pressing, wherein the compression pressure is 100MPa, and the pressure maintaining time is 300 s. Subjecting the molded green body to vacuum atmosphere (vacuum degree of 10)-1Pa), the sintering temperature is 580 ℃, the temperature is kept for 2h, and the sintering is cooled along with the furnace. And (3) carrying out hot extrusion on the sintered blank at 500 ℃, wherein the extrusion ratio is 10:1, and the low-cost powder metallurgy aluminum-lithium alloy with excellent performance is obtained.
Example 2
The lithium oxide powder was dried by heating under vacuum at 80 ℃ for 5 h. Mixing pure aluminum powder with dried lithium oxide powder, wherein the mass fraction of lithium element in the mixed powder is 3 wt.%. A silicon carbide ball milling tank and zirconia grinding balls are adopted for ball milling in a high-purity nitrogen environment, the ball-material ratio is 5:1, and the ball milling time is 4 hours. And (3) performing compression molding on the mixed aluminum lithium alloy powder by adopting isostatic cool pressing, wherein the compression pressure is 200MPa, and the pressure maintaining time is 180 s. And sintering the molded green body in high-purity nitrogen at the sintering temperature of 630 ℃, preserving heat for 7 hours, and cooling along with the furnace. And (3) carrying out hot extrusion on the sintered blank at 300 ℃, wherein the extrusion ratio is 15:1, and obtaining the low-cost powder metallurgy aluminum-lithium alloy with excellent performance.
Example 3
The lithium carbonate powder was dried by heating in a vacuum oven at 170 ℃ for 1 h. Mixing pure aluminum powder, aluminum-silicon alloy powder, aluminum-magnesium alloy powder, electrolytic copper powder and dry lithium carbonate powder, wherein the mass fraction of lithium element in the mixed powder is 0.5 wt.%. Ball milling is carried out in a high-purity argon environment by adopting a zirconium oxide ball milling tank and boron carbide grinding balls, the ball-material ratio is 3:1, and the ball milling time is 6 hours. And (3) performing compression molding on the mixed aluminum lithium alloy powder by adopting isostatic cool pressing, wherein the compression pressure is 400MPa, and the pressure maintaining time is 30 s. And sintering the molded green body in high-purity argon at 500 ℃, preserving heat for 4 hours, and cooling along with the furnace. And (3) carrying out hot extrusion on the sintered blank at the temperature of 410 ℃, wherein the extrusion ratio is 20:1, and the low-cost powder metallurgy aluminum lithium alloy with excellent performance is obtained.
Example 4
The lithium chloride powder was dried by heating in a vacuum oven at 120 ℃ for 3 h. Mixing 7050 aluminum alloy powder with dry lithium chloride powder, wherein the mass fraction of lithium element in the mixed powder is 5 wt.%. Adopts a zirconia ball milling tank and a corundum grinding ball at the vacuum degree of 10-2Ball milling is carried out in a Pa environment, the ball-material ratio is 10:1, and the ball milling time is 10 h. And (3) performing compression molding on the mixed aluminum lithium alloy powder by adopting isostatic cool pressing, wherein the compression pressure is 500MPa, and the pressure maintaining time is 120 s. Subjecting the molded green body to vacuum atmosphere (vacuum degree of 10)-2Pa), the sintering temperature is 540 ℃, the temperature is kept for 10h, and the furnace cooling is carried out. And (3) carrying out hot extrusion on the sintered blank at 350 ℃, wherein the extrusion ratio is 10:1, and the low-cost powder metallurgy aluminum-lithium alloy with excellent performance is obtained.
Claims (4)
1. A preparation method of low-cost powder metallurgy aluminum lithium alloy is characterized by comprising the following process steps:
a) preparing mixed powder: weighing one or more of pure aluminum powder, alloy element powder or alloy powder and a lithium source compound according to required components, and preparing mixed powder by ball milling, wherein the mass fraction of lithium element in the mixed powder is 0.5-5 wt%;
b) molding: the mixed aluminum lithium alloy powder is pressed and formed by adopting one or two of cold isostatic pressing or mould pressing, the pressing pressure is 100-500MPa, and the pressure maintaining time is 30-300 s;
c) and (3) sintering: sintering densification is carried out in the protective atmosphere of vacuum, nitrogen or argon, the sintering temperature is 500-630 ℃, and the heat preservation time is 1-10h, so as to obtain a compact powder metallurgy aluminum lithium alloy sintering blank;
d) deformation processing: and carrying out hot extrusion on the sintered billet at the temperature of 300-500 ℃ to obtain the low-cost powder metallurgy aluminum-lithium alloy with excellent performance.
2. The method for preparing the low-cost powder metallurgy aluminum lithium alloy according to claim 1, wherein the method comprises the following steps: the lithium source compound in the step 1) is one or more of lithium hydroxide, lithium carbonate, lithium chloride and lithium oxide.
3. The method for preparing the low-cost powder metallurgy aluminum lithium alloy according to claim 2, wherein the method comprises the following steps: the lithium source compound is dried in vacuum before mixing, the drying temperature is 80-170 ℃, and the drying time is 1-5 h.
4. The method for preparing the low-cost powder metallurgy aluminum lithium alloy according to claim 1, wherein the method comprises the following steps: preparing mixed powder by ball milling in the step 1), wherein the ball milling tank and the grinding balls are made of one or more of corundum, agate, zirconia, silicon carbide and boron carbide, and the ball milling environment is vacuum (the vacuum degree is 10)-1-10-2Pa), high-purity nitrogen and high-purity argon, wherein the ball-material ratio is 1:1-10:1, and the ball milling time is 1-10 h.
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Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN113564398A (en) * | 2021-07-06 | 2021-10-29 | 北京科技大学 | Preparation method of powder metallurgy lithium-containing aluminum-based composite material added with sintering activator |
| CN116875839A (en) * | 2023-09-06 | 2023-10-13 | 山东伟盛铝业有限公司 | Aluminum lithium alloy profile and preparation method thereof |
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| US5330704A (en) * | 1991-02-04 | 1994-07-19 | Alliedsignal Inc. | Method for producing aluminum powder alloy products having lower gas contents |
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| CN116875839A (en) * | 2023-09-06 | 2023-10-13 | 山东伟盛铝业有限公司 | Aluminum lithium alloy profile and preparation method thereof |
| CN116875839B (en) * | 2023-09-06 | 2023-12-12 | 山东伟盛铝业有限公司 | Aluminum lithium alloy profile and preparation method thereof |
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