CN114774728A - Wear-resistant aluminum alloy and preparation method thereof - Google Patents
Wear-resistant aluminum alloy and preparation method thereof Download PDFInfo
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- 229910000838 Al alloy Inorganic materials 0.000 title claims abstract description 65
- 238000002360 preparation method Methods 0.000 title claims abstract description 17
- 238000005096 rolling process Methods 0.000 claims abstract description 22
- 238000011282 treatment Methods 0.000 claims abstract description 20
- 238000009768 microwave sintering Methods 0.000 claims abstract description 18
- 238000000137 annealing Methods 0.000 claims abstract description 15
- 229910052802 copper Inorganic materials 0.000 claims abstract description 11
- 229910052759 nickel Inorganic materials 0.000 claims abstract description 11
- 229910052710 silicon Inorganic materials 0.000 claims abstract description 11
- 229910052726 zirconium Inorganic materials 0.000 claims abstract description 11
- 229910052804 chromium Inorganic materials 0.000 claims abstract description 10
- 229910052750 molybdenum Inorganic materials 0.000 claims abstract description 10
- 229910052718 tin Inorganic materials 0.000 claims abstract description 10
- 229910052720 vanadium Inorganic materials 0.000 claims abstract description 10
- 229910052748 manganese Inorganic materials 0.000 claims abstract description 9
- 238000000713 high-energy ball milling Methods 0.000 claims abstract description 5
- 229910052751 metal Inorganic materials 0.000 claims abstract description 5
- 239000002184 metal Substances 0.000 claims abstract description 5
- 238000001816 cooling Methods 0.000 claims abstract 3
- 239000000843 powder Substances 0.000 claims description 34
- 238000000498 ball milling Methods 0.000 claims description 24
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 22
- 239000000463 material Substances 0.000 claims description 19
- 239000000956 alloy Substances 0.000 claims description 18
- 229910045601 alloy Inorganic materials 0.000 claims description 17
- 238000000034 method Methods 0.000 claims description 17
- 239000007788 liquid Substances 0.000 claims description 11
- 229910052757 nitrogen Inorganic materials 0.000 claims description 11
- 238000001035 drying Methods 0.000 claims description 10
- 238000005245 sintering Methods 0.000 claims description 9
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical group CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 8
- MCMNRKCIXSYSNV-UHFFFAOYSA-N Zirconium dioxide Chemical compound O=[Zr]=O MCMNRKCIXSYSNV-UHFFFAOYSA-N 0.000 claims description 8
- 238000009694 cold isostatic pressing Methods 0.000 claims description 8
- 229910052742 iron Inorganic materials 0.000 claims description 8
- 229910052758 niobium Inorganic materials 0.000 claims description 8
- 229910052719 titanium Inorganic materials 0.000 claims description 8
- 238000010438 heat treatment Methods 0.000 claims description 5
- 238000004519 manufacturing process Methods 0.000 claims description 5
- 239000002245 particle Substances 0.000 claims description 5
- 238000005275 alloying Methods 0.000 claims description 4
- 230000006698 induction Effects 0.000 claims description 4
- 238000001291 vacuum drying Methods 0.000 claims description 4
- 238000005507 spraying Methods 0.000 claims description 3
- 238000005303 weighing Methods 0.000 claims description 3
- 238000002791 soaking Methods 0.000 claims 2
- 238000002156 mixing Methods 0.000 claims 1
- 238000004321 preservation Methods 0.000 claims 1
- PXHVJJICTQNCMI-UHFFFAOYSA-N nickel Substances [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 abstract description 15
- 239000010949 copper Substances 0.000 abstract description 11
- 239000011651 chromium Substances 0.000 abstract description 10
- 239000011135 tin Substances 0.000 abstract description 10
- XEEYBQQBJWHFJM-UHFFFAOYSA-N iron Substances [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 abstract description 9
- 239000011572 manganese Substances 0.000 abstract description 9
- 239000010936 titanium Substances 0.000 abstract description 8
- 238000005516 engineering process Methods 0.000 abstract description 5
- 238000005551 mechanical alloying Methods 0.000 abstract description 5
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 abstract description 4
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 abstract description 4
- QCWXUUIWCKQGHC-UHFFFAOYSA-N Zirconium Chemical compound [Zr] QCWXUUIWCKQGHC-UHFFFAOYSA-N 0.000 abstract description 4
- 239000010703 silicon Substances 0.000 abstract description 4
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 abstract description 3
- ZOKXTWBITQBERF-UHFFFAOYSA-N Molybdenum Chemical compound [Mo] ZOKXTWBITQBERF-UHFFFAOYSA-N 0.000 abstract description 3
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 abstract description 3
- 239000013078 crystal Substances 0.000 abstract description 3
- 239000011733 molybdenum Substances 0.000 abstract description 3
- PWHULOQIROXLJO-UHFFFAOYSA-N Manganese Chemical compound [Mn] PWHULOQIROXLJO-UHFFFAOYSA-N 0.000 abstract description 2
- 239000006104 solid solution Substances 0.000 abstract description 2
- 150000002739 metals Chemical class 0.000 abstract 1
- 230000002787 reinforcement Effects 0.000 abstract 1
- 239000000126 substance Substances 0.000 abstract 1
- LEONUFNNVUYDNQ-UHFFFAOYSA-N vanadium atom Chemical compound [V] LEONUFNNVUYDNQ-UHFFFAOYSA-N 0.000 abstract 1
- 239000000203 mixture Substances 0.000 description 9
- 230000000052 comparative effect Effects 0.000 description 8
- 238000012360 testing method Methods 0.000 description 8
- 239000010955 niobium Substances 0.000 description 7
- 230000008569 process Effects 0.000 description 5
- 229910000831 Steel Inorganic materials 0.000 description 4
- 230000006872 improvement Effects 0.000 description 4
- 238000002844 melting Methods 0.000 description 4
- 230000008018 melting Effects 0.000 description 4
- 239000010959 steel Substances 0.000 description 4
- 229910001008 7075 aluminium alloy Inorganic materials 0.000 description 3
- 229910052782 aluminium Inorganic materials 0.000 description 3
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 3
- 230000008901 benefit Effects 0.000 description 3
- 230000007797 corrosion Effects 0.000 description 3
- 238000005260 corrosion Methods 0.000 description 3
- 238000002474 experimental method Methods 0.000 description 3
- 238000011056 performance test Methods 0.000 description 3
- 238000007745 plasma electrolytic oxidation reaction Methods 0.000 description 3
- 230000003068 static effect Effects 0.000 description 3
- 238000005266 casting Methods 0.000 description 2
- 230000007547 defect Effects 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 238000003912 environmental pollution Methods 0.000 description 2
- 238000000227 grinding Methods 0.000 description 2
- 238000004372 laser cladding Methods 0.000 description 2
- 239000000314 lubricant Substances 0.000 description 2
- 238000001755 magnetron sputter deposition Methods 0.000 description 2
- WPBNNNQJVZRUHP-UHFFFAOYSA-L manganese(2+);methyl n-[[2-(methoxycarbonylcarbamothioylamino)phenyl]carbamothioyl]carbamate;n-[2-(sulfidocarbothioylamino)ethyl]carbamodithioate Chemical compound [Mn+2].[S-]C(=S)NCCNC([S-])=S.COC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OC WPBNNNQJVZRUHP-UHFFFAOYSA-L 0.000 description 2
- 238000012545 processing Methods 0.000 description 2
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- 239000000243 solution Substances 0.000 description 2
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- 238000004381 surface treatment Methods 0.000 description 2
- GPPXJZIENCGNKB-UHFFFAOYSA-N vanadium Chemical compound [V]#[V] GPPXJZIENCGNKB-UHFFFAOYSA-N 0.000 description 2
- 229910000733 Li alloy Inorganic materials 0.000 description 1
- 229910000861 Mg alloy Inorganic materials 0.000 description 1
- 238000003723 Smelting Methods 0.000 description 1
- 229910001069 Ti alloy Inorganic materials 0.000 description 1
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 1
- 239000003082 abrasive agent Substances 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 229910052783 alkali metal Inorganic materials 0.000 description 1
- 150000001340 alkali metals Chemical class 0.000 description 1
- JRBRVDCKNXZZGH-UHFFFAOYSA-N alumane;copper Chemical class [AlH3].[Cu] JRBRVDCKNXZZGH-UHFFFAOYSA-N 0.000 description 1
- CSDREXVUYHZDNP-UHFFFAOYSA-N alumanylidynesilicon Chemical compound [Al].[Si] CSDREXVUYHZDNP-UHFFFAOYSA-N 0.000 description 1
- -1 aluminum-zinc-magnesium-copper series Chemical class 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 230000015556 catabolic process Effects 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 238000006731 degradation reaction Methods 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 230000009977 dual effect Effects 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
- 238000007654 immersion Methods 0.000 description 1
- 239000001989 lithium alloy Substances 0.000 description 1
- 238000005461 lubrication Methods 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 239000003607 modifier Substances 0.000 description 1
- 239000002159 nanocrystal Substances 0.000 description 1
- GUCVJGMIXFAOAE-UHFFFAOYSA-N niobium atom Chemical compound [Nb] GUCVJGMIXFAOAE-UHFFFAOYSA-N 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 238000005728 strengthening Methods 0.000 description 1
- 229910052712 strontium Inorganic materials 0.000 description 1
- CIOAGBVUUVVLOB-UHFFFAOYSA-N strontium atom Chemical compound [Sr] CIOAGBVUUVVLOB-UHFFFAOYSA-N 0.000 description 1
- 230000009466 transformation Effects 0.000 description 1
- 238000003466 welding Methods 0.000 description 1
- 229910052727 yttrium Inorganic materials 0.000 description 1
- VWQVUPCCIRVNHF-UHFFFAOYSA-N yttrium atom Chemical compound [Y] VWQVUPCCIRVNHF-UHFFFAOYSA-N 0.000 description 1
Classifications
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- 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
- C21—METALLURGY OF IRON
- C21D—MODIFYING THE PHYSICAL STRUCTURE OF FERROUS METALS; GENERAL DEVICES FOR HEAT TREATMENT OF FERROUS OR NON-FERROUS METALS OR ALLOYS; MAKING METAL MALLEABLE, e.g. BY DECARBURISATION OR TEMPERING
- C21D1/00—General methods or devices for heat treatment, e.g. annealing, hardening, quenching or tempering
- C21D1/04—General methods or devices for heat treatment, e.g. annealing, hardening, quenching or tempering with simultaneous application of supersonic waves, magnetic or electric fields
-
- 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
- C22C21/02—Alloys based on aluminium with silicon as the next major constituent
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22F—CHANGING THE PHYSICAL STRUCTURE OF NON-FERROUS METALS AND NON-FERROUS ALLOYS
- C22F1/00—Changing the physical structure of non-ferrous metals or alloys by heat treatment or by hot or cold working
- C22F1/02—Changing the physical structure of non-ferrous metals or alloys by heat treatment or by hot or cold working in inert or controlled atmosphere or vacuum
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22F—CHANGING THE PHYSICAL STRUCTURE OF NON-FERROUS METALS AND NON-FERROUS ALLOYS
- C22F1/00—Changing the physical structure of non-ferrous metals or alloys by heat treatment or by hot or cold working
- C22F1/04—Changing the physical structure of non-ferrous metals or alloys by heat treatment or by hot or cold working of aluminium or alloys based thereon
- C22F1/043—Changing the physical structure of non-ferrous metals or alloys by heat treatment or by hot or cold working of aluminium or alloys based thereon of alloys with silicon as the next major constituent
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P10/00—Technologies related to metal processing
- Y02P10/25—Process efficiency
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- Metallurgy (AREA)
- Organic Chemistry (AREA)
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- Thermal Sciences (AREA)
- Crystallography & Structural Chemistry (AREA)
- Powder Metallurgy (AREA)
Abstract
Description
技术领域technical field
本发明属于铝合金材料领域,具体涉及一种新型高耐磨铝合金及其制备方法。The invention belongs to the field of aluminum alloy materials, and particularly relates to a novel high wear-resistant aluminum alloy and a preparation method thereof.
背景技术Background technique
铝合金密度低,但强度比较高,接近或超过优质钢,塑性好,可加工成各种型材,具有优良的导电性、导热性和抗蚀性,工业上广泛使用,使用量仅次于钢;但是铝合金的耐磨性能和硬度一般低于其他合金,这导致了其适用范围受限。Aluminum alloy has low density, but relatively high strength, close to or surpassing high-quality steel, good plasticity, can be processed into various profiles, has excellent electrical conductivity, thermal conductivity and corrosion resistance, widely used in industry, second only to steel However, the wear resistance and hardness of aluminum alloys are generally lower than those of other alloys, which leads to a limited range of applications.
随着世界各国对能源需求的日益扩大,密度小、比强度和比刚度高的材料越来越受到设计者和材料科技工作者的重视;目前,世界各国研究的轻量化材料主要有:铝合金、镁合金、锂合金和钛合金等;由于铝的资源丰富,并且铝合金具有密度小、强度重量比大、耐腐蚀性能强、加工性能和焊接性能好等特点,使铝合金已经广泛地应用于航空、航天、汽车、机械等各领域;以铝代钢可以大大减轻零件的重量、节约能源、降低成本和减少环境污染。With the increasing demand for energy in various countries in the world, materials with low density, high specific strength and specific stiffness have been paid more and more attention by designers and material scientists. , magnesium alloys, lithium alloys and titanium alloys, etc.; due to the rich resources of aluminum, and the characteristics of aluminum alloys with low density, large strength-to-weight ratio, strong corrosion resistance, good processing performance and welding performance, aluminum alloys have been widely used. Used in aviation, aerospace, automobile, machinery and other fields; replacing steel with aluminum can greatly reduce the weight of parts, save energy, reduce costs and reduce environmental pollution.
对于航空、航天产品而言,提高飞机、导弹等性能的重要环节就是对其结构部件的减重;铝合金作为航空产品的主要结构材料之一,适用于铸造生产形状复杂、比强度要求高、整体性能要求均一的零件;在现代汽车工业,由于能源、环境、安全方面的原因,对汽车轻量化的要求也越来越迫切;铝合金作为汽车轻量化的首选材料,已经广泛应用于汽车的底盘、车身、发动机、转向系统、制动器及各种附件。For aviation and aerospace products, an important part of improving the performance of aircraft and missiles is to reduce the weight of their structural components; aluminum alloy, as one of the main structural materials of aviation products, is suitable for casting production with complex shapes, high specific strength requirements, Parts with uniform overall performance are required; in the modern automobile industry, due to energy, environmental and safety reasons, the requirements for lightweight automobiles are becoming more and more urgent; as the preferred material for lightweight automobiles, aluminum alloys have been widely used in automobiles. Chassis, body, engine, steering system, brakes and various accessories.
然而,作为机械部件材料的铝合金本身具有硬度低、耐磨损性能差、摩擦系数高、不容易润滑等缺陷,这些都大大限制了铝合金的应用范围;因为铝合金表面耐磨损性能差,导致工件的使用寿命缩短;又由于铝合金表面摩擦系数高,既加速了自身的磨损、增加了能量的损耗、也导致了对偶材料的磨损;因此,改善铝合金表面的摩擦学性能有利于节约能源、降低成本、提高生产率和经济效益。However, the aluminum alloy itself as a material for mechanical parts has defects such as low hardness, poor wear resistance, high friction coefficient, and not easy lubrication, which greatly limit the application range of aluminum alloys; because the surface wear resistance of aluminum alloys is poor. , resulting in a shortened service life of the workpiece; and due to the high friction coefficient of the aluminum alloy surface, it not only accelerates its own wear, increases the energy loss, but also leads to the wear of the dual material; therefore, improving the tribological properties of the aluminum alloy surface is conducive to Save energy, reduce costs, increase productivity and economic efficiency.
近年来,为了改善铝合金表面的摩擦学性能,许多学者对铝合金进行了一些表面处理,这些表面处理方法主要有:表面喷涂、磁控溅射、激光熔覆、粘结固体润滑剂、阳极氧化和微弧氧化等;表面喷涂虽然工艺较简单,但是所得膜层的硬度、致密性和膜基结合力通常难以达到理想的效果;磁控溅射和激光熔覆往往需要较高的处理温度,这样容易造成基体的退化,而且这两种工艺的成本太高;在铝合金基体上粘结的固体润滑剂膜层并没有一定的硬度,不适合重载的工况应用条件;阳极氧化膜层的厚度和硬度还不够要求,而且前处理过程复杂,处理过程对温度要求严格;微弧氧化因其特殊的成膜原理和成膜过程,制备的膜层不可避免的存在微孔及微裂纹、表面粗糙、主要物相耐酸腐蚀性差等缺点,这限制了微弧氧化膜层性能的改善。In recent years, in order to improve the tribological properties of aluminum alloy surfaces, many scholars have carried out some surface treatments on aluminum alloys. These surface treatment methods mainly include: surface spraying, magnetron sputtering, laser cladding, bonded solid lubricants, anodes Oxidation and micro-arc oxidation, etc.; although the surface spraying process is relatively simple, the hardness, compactness and bonding force of the obtained film are usually difficult to achieve the desired effect; magnetron sputtering and laser cladding often require higher processing temperatures , it is easy to cause the degradation of the substrate, and the cost of these two processes is too high; the solid lubricant film layer bonded on the aluminum alloy substrate does not have a certain hardness, which is not suitable for heavy-duty working conditions; anodized film The thickness and hardness of the layer are not enough, and the pretreatment process is complicated, and the treatment process has strict requirements on temperature; because of the special film-forming principle and film-forming process of micro-arc oxidation, the prepared film inevitably has micropores and microcracks , rough surface, poor acid corrosion resistance of the main phase, etc., which limit the improvement of the performance of the micro-arc oxidation film.
发明内容SUMMARY OF THE INVENTION
本发明的目的在于提供一种新型高耐磨的铝合金及其制备方法,解决现有铝合金耐磨性不佳、硬度较低的问题。The purpose of the present invention is to provide a novel high wear-resistant aluminum alloy and a preparation method thereof, so as to solve the problems of poor wear resistance and low hardness of the existing aluminum alloys.
本发明的目的是通过以下技术方案实现的:The purpose of this invention is to realize through the following technical solutions:
一种耐磨铝合金的制备方法,其特征在于,包括以下步骤:A preparation method of wear-resistant aluminum alloy, characterized in that, comprising the following steps:
步骤(1)称量铝合金粉末:将Si、Zr、Ti、Cu、Sn、Mn、Nb、Fe、Ni、 Cr、V、Mo的粉末,按照以下质量百分比组成称量混合,10.4~11.8%的Si、1.5~2.5%的Zr、1.2~2.2%的Ti、0.05~0.1%的Cu、1.2~1.7%的Sn、0.5~0.7%的Mn、1.4~2.4%的Nb、0.07~0.2%的Fe、0.03~0.15%的Ni、0.05~0.15%的Cr、0.14~0.22%的V、0.2~0.25%的Mo,余量为Al;粉末的粒度在100-200目;Step (1) Weighing the aluminum alloy powder: the powders of Si, Zr, Ti, Cu, Sn, Mn, Nb, Fe, Ni, Cr, V, Mo are weighed and mixed according to the following mass percentages, 10.4-11.8% Si, 1.5-2.5% Zr, 1.2-2.2% Ti, 0.05-0.1% Cu, 1.2-1.7% Sn, 0.5-0.7% Mn, 1.4-2.4% Nb, 0.07-0.2% Fe, 0.03-0.15% Ni, 0.05-0.15% Cr, 0.14-0.22% V, 0.2-0.25% Mo, the balance is Al; the particle size of the powder is 100-200 mesh;
步骤(2)高能球磨合金化:混合的金属粉末装入氧化锆球磨罐中,将球磨罐抽真空,采用行星式球磨机进行球磨、干燥后,获得合金化的铝合金粉末;Step (2) high-energy ball milling alloying: the mixed metal powder is loaded into a zirconia ball mill jar, the ball mill jar is evacuated, and the alloyed aluminum alloy powder is obtained after ball milling and drying with a planetary ball mill;
步骤(3)冷等静压成型:将步骤(2)制备的铝合金粉末放入橡胶模具中进行冷等静压成型,静压力400MPa,保压时间30min,得到生坯;Step (3) cold isostatic pressing: put the aluminum alloy powder prepared in step (2) into a rubber mold for cold isostatic pressing, with a static pressure of 400 MPa and a holding time of 30 minutes to obtain a green body;
步骤(4)微波烧结:将步骤(3)所得的生坯放入微波烧结马弗炉中进行微波烧结;Step (4) microwave sintering: put the green body obtained in step (3) into a microwave sintering muffle furnace for microwave sintering;
步骤(5)低温轧制:将步骤(4)所得的微波烧结试样放入液氮中浸泡,之后进行低温轧制;Step (5) low-temperature rolling: put the microwave sintered sample obtained in step (4) into liquid nitrogen for immersion, and then perform low-temperature rolling;
步骤(6)真空退火:将步骤(5)低温轧制之后的试样进行真空退火处理;Step (6) vacuum annealing: vacuum annealing the sample after the low temperature rolling in step (5);
步骤(7)磁场深冷处理:将步骤(6)所得的试样放入磁场中进行深冷处理。Step (7) Magnetic field cryogenic treatment: put the sample obtained in step (6) into a magnetic field for cryogenic treatment.
进一步地,所述步骤(2)中,磨球时,球磨球按照15mm大球、10mm中球、5mm小球的数量按质量比1:2:4来配比,球料比按5:1,球磨介质为无水乙醇,无水乙醇与粉料比为3:5。Further, in the step (2), when grinding the balls, the ball grinding balls are proportioned according to the mass ratio of 1:2:4 according to the number of 15mm large balls, 10mm medium balls and 5mm small balls, and the ball-to-material ratio is 5:1 , the ball milling medium is anhydrous ethanol, and the ratio of anhydrous ethanol to powder is 3:5.
进一步地,球磨转速为320~400r/min,球磨时间为8~12个小时;当球磨结束后,将制备好的合金粉末用真空干燥箱干燥,干燥温度70~80℃,干燥时间 36h。Further, the ball milling speed is 320-400 r/min, and the ball-milling time is 8-12 hours; when the ball-milling is finished, the prepared alloy powder is dried in a vacuum drying oven at a drying temperature of 70-80 °C and a drying time of 36 hours.
进一步地,步骤(4)中所述微波烧结采用的参数为:升温速率为35~50℃ /min,烧结温度为570~700℃,烧结时间为60~80min。Further, the parameters used in the microwave sintering in step (4) are: the heating rate is 35-50° C./min, the sintering temperature is 570-700° C., and the sintering time is 60-80 min.
进一步地,步骤(5)中轧制前先将试样浸泡于液氮中保持10~20min,使试样温度降低至液氮温度;轧制过程中在轧辊上喷淋液氮;轧制的变形量为 10%~70%。Further, in step (5), before rolling, the sample is immersed in liquid nitrogen for 10-20 minutes, so that the temperature of the sample is lowered to the temperature of liquid nitrogen; during the rolling process, liquid nitrogen is sprayed on the roll; The amount of deformation is 10% to 70%.
进一步地,步骤(6)中所述的真空退火是:在真空条件下采用分步退火,第一步在400~500℃,保温时间1~3h,然后空冷至室温,第二步在220~300℃,保温20~40min,然后空冷至室温。Further, the vacuum annealing described in step (6) is: adopting step-by-step annealing under vacuum conditions, the first step is at 400~500°C, the holding time is 1~3h, then air-cooled to room temperature, and the second step is at 220~500°C 300℃, keep warm for 20-40min, and then air-cool to room temperature.
进一步地,步骤(7)中所述的磁场深冷处理所采用的磁场为脉冲磁场,磁感应强度为2.5~3T,脉冲数30次。Further, the magnetic field used in the magnetic field cryogenic treatment described in step (7) is a pulsed magnetic field, the magnetic induction intensity is 2.5-3T, and the number of pulses is 30 times.
进一步地,步骤(7)中所述的磁场深冷处理的温度为-110℃~-196℃,深冷时间为24~48小时。Further, the temperature of the magnetic field cryogenic treatment in step (7) is -110°C to -196°C, and the cryogenic time is 24 to 48 hours.
所述制备方法制备的耐磨铝合金。The wear-resistant aluminum alloy prepared by the preparation method.
本发明的有益效果为:The beneficial effects of the present invention are:
1)本发明通过多元素微合金化,提高合金的硬度和耐磨性,在合金中添加硅、锆、钛、铜、锡、锰、铌、铁、镍、铬、钒和钼元素,能显著提高铝合金的耐磨性能。与现有的铝-硅系铸造耐磨铝合金和铝-锌-镁-铜系、铝-铜系高强耐磨铝合金相比,不使用资源少、价格高的钇、锶等稀土类、碱金属类变质剂,降低环境污染和成本;本发明通过优选硅、锆、铜、镍、锰等元素的含量,并加入铬、钒、钼、锡元素,这些元素与铝、硅、锆、铜、镍、锰易于通过机械合金化的方法生成高强韧耐磨合金;材料的抗拉强度提高到800MPa以上,比现有的高强铝合金提高约30%以上,合金硬度高、弥散强化相细小,耐磨性比七系耐磨铝合金显著提高,约18.09%。1) The present invention improves the hardness and wear resistance of the alloy through multi-element microalloying, and adds elements of silicon, zirconium, titanium, copper, tin, manganese, niobium, iron, nickel, chromium, vanadium and molybdenum to the alloy, which can improve the hardness and wear resistance of the alloy. Significantly improve the wear resistance of aluminum alloys. Compared with the existing aluminum-silicon cast wear-resistant aluminum alloys and aluminum-zinc-magnesium-copper series and aluminum-copper series high-strength wear-resistant aluminum alloys, it does not use rare earths such as yttrium, strontium and other rare earths with less resources and high prices. Alkali metal modifiers reduce environmental pollution and cost; the present invention optimizes the content of elements such as silicon, zirconium, copper, nickel, and manganese, and adds chromium, vanadium, molybdenum, and tin elements, which are combined with aluminum, silicon, zirconium, Copper, nickel and manganese are easy to form high-strength, tough and wear-resistant alloys by mechanical alloying; the tensile strength of the material is increased to more than 800MPa, which is about 30% higher than the existing high-strength aluminum alloys. The alloy has high hardness and fine dispersion strengthening phase. , The wear resistance is significantly higher than that of the seven series wear-resistant aluminum alloy, about 18.09%.
2)相比于传统的熔融制备方法,本发明所用的机械合金化是一种通过非平衡的手段进行不同元素的原子与原子之间的强行固溶,最后可以获得晶粒细小、成分和组织分布均匀的合金粉末的化合技术;机械合金化的优点在于它能够不用考虑原料的熔点问题,不论是熔化温度过高还是熔点差别过大,都能够有效地解决使它们化合在一起,而且得到的合金成分均匀不存在偏析的现象,用这种方法制备的合金不会存在缩松缩孔的问题,而且合金的晶粒尺寸比较细小,能够有效地提高铝合金的硬度和耐磨性。2) Compared with the traditional melting preparation method, the mechanical alloying used in the present invention is a kind of forced solid solution between atoms of different elements through non-equilibrium means, and finally, fine grains, composition and structure can be obtained. The compound technology of uniformly distributed alloy powder; the advantage of mechanical alloying is that it can effectively solve the problem of combining them without considering the melting point of the raw materials, whether the melting temperature is too high or the melting point difference is too large, and the obtained The alloy composition is uniform and there is no segregation phenomenon. The alloy prepared by this method does not have the problem of shrinkage porosity, and the grain size of the alloy is relatively small, which can effectively improve the hardness and wear resistance of the aluminum alloy.
3)本发明中,运用了微波烧结技术,其拥有低温快烧的优点,可使材料内部形成均匀的细晶结构和高致密性,从而改善材料性能;同时微波烧结加热时,材料各部分几乎没有温差,颗粒均匀地分布在粉末中,几乎没有诸如偏析等缺陷,并且极大地改善了铝合金性能。3) In the present invention, the microwave sintering technology is used, which has the advantages of low temperature and fast sintering, and can form a uniform fine-grained structure and high density inside the material, thereby improving the material properties; There is no temperature difference, the particles are uniformly distributed in the powder, there are almost no defects such as segregation, and the aluminum alloy properties are greatly improved.
4)本发明中,运用了液氮低温轧制,随着轧制变形量的提高,材料的强度和塑性同时提高,强度的提高是因为塑性变形引起了位错密度的增加,塑性的提高是因为高密度的预存位错在应力作用下开动并形成了纳米晶和亚晶。4) In the present invention, liquid nitrogen low-temperature rolling is used. With the increase of rolling deformation, the strength and plasticity of the material are improved at the same time. The improvement of strength is due to the increase of dislocation density caused by plastic deformation, and the improvement of plasticity is Because of the high density of pre-existing dislocations under stress, nanocrystals and subcrystals are formed.
5)本发明中,运用了,促进孪晶和亚晶组织生成,促进相变,提高材料致密度,从而提高了材料的耐磨性。5) In the present invention, it is used to promote the formation of twin crystals and sub-crystal structures, promote phase transformation, and improve the density of the material, thereby improving the wear resistance of the material.
具体实施方式Detailed ways
为使本领域技术人员更好地理解本发明的技术方案,这些实施例只是为了举例说明本发明,而非以任何方式限制本发明的范围;在以下的实施例中,未详细描述的各种过程和方法是本领域中公知的常规方法。In order to make those skilled in the art better understand the technical solutions of the present invention, these embodiments are only for illustrating the present invention, rather than limiting the scope of the present invention in any way; The procedures and methods are conventional methods well known in the art.
铝合金的显微硬度实验在数显显微硬度计上进行;铝合金的磨损实验在 MMU-5GA微机控制高温摩擦磨损试验机上进行;试样尺寸:4.8mm×12.7mm的销试样,对磨材料为GCr15钢加工成D54mm×8mm的盘试样;采用干滑动摩擦磨损,实验温度采取25℃,载荷选取150N,转动速度为50r/min,磨损时间为20min;耐磨性用磨损失重来表达。The microhardness test of aluminum alloy was carried out on a digital microhardness tester; the wear test of aluminum alloy was carried out on a MMU-5GA microcomputer-controlled high-temperature friction and wear tester; sample size: 4.8mm×12.7mm pin sample, for The abrasive material is GCr15 steel processed into a D54mm×8mm disk sample; dry sliding friction and wear are used, the experimental temperature is 25°C, the load is 150N, the rotation speed is 50r/min, and the wear time is 20min; the wear resistance is based on wear loss. Express.
实施例1:Example 1:
本实施例中的耐磨铝合金的组成为:10.4%的Si、1.5%的Zr、1.2%的Ti、0.05%的Cu、1.2%的Sn、0.5%的Mn、1.4%的Nb、0.07%的Fe、0.03%的Ni、0.05%的 Cr、0.14%的V、0.2%的Mo,余量为Al。The composition of the wear-resistant aluminum alloy in this embodiment is: 10.4% Si, 1.5% Zr, 1.2% Ti, 0.05% Cu, 1.2% Sn, 0.5% Mn, 1.4% Nb, 0.07% Fe, 0.03% Ni, 0.05% Cr, 0.14% V, 0.2% Mo, and the balance is Al.
本发明的耐磨铝合金的制备方法采用以下步骤:The preparation method of the wear-resistant aluminum alloy of the present invention adopts the following steps:
步骤(1)、配制铝合金粉末:Step (1), prepare aluminum alloy powder:
将Si、Zr、Ti、Cu、Sn、Mn、Nb、Fe、Ni、Cr、V、Mo的粉末,按照所述权利要求1的质量百分比组成配制,所有这些粉末的粒度在100-200目,纯度为 99.9%级别。The powders of Si, Zr, Ti, Cu, Sn, Mn, Nb, Fe, Ni, Cr, V, and Mo are prepared according to the mass percentage composition of claim 1, and the particle size of all these powders is 100-200 mesh, The purity is 99.9% grade.
步骤(2)、高能球磨合金化:Step (2), high-energy ball milling alloying:
按照步骤(1)配制的金属粉末装入氧化锆球磨罐中,然后将球磨罐抽真空,采用行星式球磨机进行球磨,磨球按直径分三个级别,大球:15mm;中球:10mm;小球:5mm,球磨球数量配比按质量比1:2:4,球料比按5:1,球磨介质为无水乙醇,无水乙醇与粉料比为3:5,球磨转速为400r/min,球磨时间为10个小时;当球磨结束后,将制备好的合金粉末用真空干燥箱干燥,干燥温度75℃,干燥时间36h,获得合金化粉末。The metal powder prepared according to step (1) is put into a zirconia ball mill jar, then the ball mill jar is evacuated, and a planetary ball mill is used for ball milling. Small ball: 5mm, the ratio of ball mill balls is 1:2:4 by mass, the ratio of ball to material is 5:1, the ball milling medium is anhydrous ethanol, the ratio of anhydrous ethanol to powder is 3:5, and the ball milling speed is 400r /min, the ball milling time is 10 hours; when the ball milling is finished, the prepared alloy powder is dried in a vacuum drying oven, the drying temperature is 75 °C, and the drying time is 36 h to obtain alloyed powder.
步骤(3)、冷等静压成型:Step (3), cold isostatic pressing:
将步骤(2)制备的合金化粉末放入橡胶模具中进行冷等静压成型,静压力400MPa,保压时间30min,得到生坯。The alloyed powder prepared in step (2) is put into a rubber mold for cold isostatic pressing with a static pressure of 400 MPa and a pressure holding time of 30 minutes to obtain a green body.
步骤(4)、微波烧结:Step (4), microwave sintering:
将步骤(3)所得的生坯放入微波烧结马弗炉中进行微波烧结,烧结温度为 570℃,烧结时间为80min,升温速率为35℃/min。The green body obtained in step (3) is put into a microwave sintering muffle furnace for microwave sintering, the sintering temperature is 570°C, the sintering time is 80min, and the heating rate is 35°C/min.
步骤(5)、低温轧制:Step (5), low temperature rolling:
将步骤(4)所得的微波烧结试样放入液氮中浸泡10min,之后进行低温轧制,轧制的变形量为20%。The microwave sintered sample obtained in step (4) was soaked in liquid nitrogen for 10 minutes, and then low-temperature rolling was performed, and the rolling deformation amount was 20%.
步骤(6)、真空退火:Step (6), vacuum annealing:
将步骤(5)低温轧制之后的试样进行真空退火处理,在真空条件下采用分步退火,第一步在400℃,保温时间2h,然后空冷至室温,第二步在220℃,保温30min,然后空冷至室温。The sample after low-temperature rolling in step (5) is subjected to vacuum annealing treatment, and step-by-step annealing is adopted under vacuum conditions. 30min, then air-cooled to room temperature.
步骤(7)、磁场深冷处理:Step (7), magnetic field cryogenic treatment:
将步骤(6)所得的试样放入磁场中进行深冷处理,磁场为脉冲磁场,磁感应强度为2.5T,脉冲数30次;深冷处理的温度为-110℃,深冷时间为24h。Put the sample obtained in step (6) into a magnetic field for cryogenic treatment, the magnetic field is a pulsed magnetic field, the magnetic induction intensity is 2.5T, and the number of pulses is 30 times; the cryogenic treatment temperature is -110°C, and the cryogenic time is 24h.
对实施例1制备的铝合金进行摩擦磨损试验和显微硬度试验,实验结果如表1所示。A friction and wear test and a microhardness test were performed on the aluminum alloy prepared in Example 1, and the experimental results are shown in Table 1.
实施例2:Example 2:
本实施例的耐磨铝合金的组成为:10.9%的Si、2%的Zr、1.7%的Ti、0.07%的Cu、1.5%的Sn、0.6%的Mn、1..7%的Nb、0.15%的Fe、0.12%的Ni、0.1%的 Cr、0.19%的V、0.21%的Mo,余量为Al。The composition of the wear-resistant aluminum alloy of this embodiment is: 10.9% Si, 2% Zr, 1.7% Ti, 0.07% Cu, 1.5% Sn, 0.6% Mn, 1..7% Nb, 0.15% Fe, 0.12% Ni, 0.1% Cr, 0.19% V, 0.21% Mo, and the balance is Al.
本发明的耐磨铝合金的制备方法采用以下步骤:The preparation method of the wear-resistant aluminum alloy of the present invention adopts the following steps:
步骤(1)、配制铝合金粉末:Step (1), prepare aluminum alloy powder:
将Si、Zr、Ti、Cu、Sn、Mn、Nb、Fe、Ni、Cr、V、Mo的粉末,按照所述权利要求1的质量百分比组成配制,所有这些粉末的粒度在100-200目,纯度为 99.9%级别。The powders of Si, Zr, Ti, Cu, Sn, Mn, Nb, Fe, Ni, Cr, V, and Mo are prepared according to the mass percentage composition of claim 1, and the particle size of all these powders is 100-200 mesh, The purity is 99.9% grade.
步骤(2)、高能球磨合金化:Step (2), high-energy ball milling alloying:
按照步骤(1)配制的金属粉末装入氧化锆球磨罐中,然后将球磨罐抽真空,采用行星式球磨机进行球磨,磨球按直径分三个级别,大球:15mm;中球:10mm;小球:5mm,球磨球数量配比按质量比1:2:4,球料比按5:1,球磨介质为无水乙醇,无水乙醇与粉料比为3:5,球磨转速为400r/min,球磨时间为10个小时;当球磨结束后,将制备好的合金粉末用真空干燥箱干燥,干燥温度75℃,干燥时间36h,获得合金化粉末。The metal powder prepared according to step (1) is put into a zirconia ball mill jar, then the ball mill jar is evacuated, and a planetary ball mill is used for ball milling. Small ball: 5mm, the ratio of ball mill balls is 1:2:4 by mass, the ratio of ball to material is 5:1, the ball milling medium is anhydrous ethanol, the ratio of anhydrous ethanol to powder is 3:5, and the ball milling speed is 400r /min, the ball milling time is 10 hours; when the ball milling is finished, the prepared alloy powder is dried in a vacuum drying oven, the drying temperature is 75 °C, and the drying time is 36 h to obtain alloyed powder.
步骤(3)、冷等静压成型:Step (3), cold isostatic pressing:
将步骤(2)制备的合金化粉末放入橡胶模具中进行冷等静压成型,静压力400MPa,保压时间30min,得到生坯。The alloyed powder prepared in step (2) is put into a rubber mold for cold isostatic pressing with a static pressure of 400 MPa and a pressure holding time of 30 minutes to obtain a green body.
步骤(4)、微波烧结:Step (4), microwave sintering:
将步骤(3)所得的生坯放入微波烧结马弗炉中进行微波烧结,烧结温度为 620℃,烧结时间为70min,升温速率为40℃/min。The green body obtained in step (3) is put into a microwave sintering muffle furnace for microwave sintering, the sintering temperature is 620°C, the sintering time is 70min, and the heating rate is 40°C/min.
步骤(5)、低温轧制:Step (5), low temperature rolling:
将步骤(4)所得的微波烧结试样放入液氮中浸泡15min,之后进行低温轧制,轧制的变形量为45%。The microwave sintered sample obtained in step (4) was soaked in liquid nitrogen for 15 minutes, and then low-temperature rolling was performed, and the rolling deformation amount was 45%.
步骤(6)、真空退火:Step (6), vacuum annealing:
将步骤(5)低温轧制之后的试样进行真空退火处理,在真空条件下采用分步退火,第一步在450℃,保温时间1h,然后空冷至室温,第二步在250℃,保温20min,然后空冷至室温。The sample after low-temperature rolling in step (5) is subjected to vacuum annealing treatment, and step-by-step annealing is adopted under vacuum conditions. 20min, then air-cooled to room temperature.
步骤(7)、磁场深冷处理:Step (7), magnetic field cryogenic treatment:
将步骤(6)所得的试样放入磁场中进行深冷处理,磁场为脉冲磁场,磁感应强度为3T,脉冲数30次;深冷处理的温度为-196℃,深冷时间为36h。The sample obtained in step (6) is placed in a magnetic field for cryogenic treatment, the magnetic field is a pulsed magnetic field, the magnetic induction intensity is 3T, and the number of pulses is 30 times; the cryogenic treatment temperature is -196°C, and the cryogenic time is 36h.
对实施例2制备的铝合金进行摩擦磨损试验和显微硬度试验,实验结果如表1所示。A friction and wear test and a microhardness test were performed on the aluminum alloy prepared in Example 2, and the experimental results are shown in Table 1.
对比例1:Comparative Example 1:
为说明本发明的技术效果,选择商业化7075铝合金进行性能对比实验,对比例1采用市售的7075变形铝合金,对其进行摩擦磨损试验和显微硬度实验,方法详见具体实施方式,实验结果如表1所示。In order to illustrate the technical effect of the present invention, commercialized 7075 aluminum alloy is selected to carry out a performance comparison experiment. Comparative example 1 adopts a commercially available 7075 deformed aluminum alloy, and carries out a friction and wear test and a microhardness test. The method is detailed in the specific embodiments. The experimental results are shown in Table 1.
对比例2:Comparative Example 2:
采用与实施例1完全相同的铝合金成分,采用熔炼合金化-吹气精炼-半连铸成型-T6热处理的传统生产耐磨铝合金的方法制备了铝合金铸坯,取铸坯试样进行与对实施例1完全相同的性能测试实验,得到对比例2的实验对比数据,汇总至表1,从对比结果可知,采用本发明的制备方法,材料耐磨性和硬度都有显著提升。Using the exact same aluminum alloy composition as in Example 1, the aluminum alloy casting billet was prepared by the traditional method of producing wear-resistant aluminum alloy by smelting alloying-air refining-semi-continuous casting-T6 heat treatment. The same performance test experiment as in Example 1 was carried out, and the experimental comparison data of Comparative Example 2 were obtained, which were summarized in Table 1. From the comparison results, it can be seen that the wear resistance and hardness of the material were significantly improved by using the preparation method of the present invention.
对比例3:Comparative Example 3:
采用与对比例1完全相同的7075铝合金成分,只采用本发明的制备方法,制备过程与实施例2完全相同,获得了7075铝合金块体,取对比例3的试样进行与对实施例2完全相同的性能测试实验,得到对比例3的实验对比数据,汇总至表1,从对比结果可知,采用本发明的制备方法,材料耐磨性和硬度都有显著提升。The same 7075 aluminum alloy composition as in Comparative Example 1 was used, and only the preparation method of the present invention was used. The preparation process was exactly the same as that in Example 2, and a 7075 aluminum alloy block was obtained. 2. The same performance test experiment was carried out, and the experimental comparison data of Comparative Example 3 was obtained, which was summarized in Table 1. It can be seen from the comparison results that the wear resistance and hardness of the material were significantly improved by the preparation method of the present invention.
表1不同铝合金摩擦磨损性能和显微硬度Table 1 Friction and wear properties and microhardness of different aluminum alloys
通过表1的实施例和对比例的性能测试结果对比可以看出,由本发明耐磨铝合金及制备方法,相对比与目前商业化的耐磨铝合金在成分和制备方法方面都具有性能方面的优势,体现了本发明的进步性,也就是按照本发明,能够制备出一种具有高耐磨性的铝合金。It can be seen from the comparison of the performance test results of the examples in Table 1 and the comparative examples that the wear-resistant aluminum alloy of the present invention and the preparation method are relatively comparable to the current commercial wear-resistant aluminum alloys in terms of composition and preparation method. The advantages reflect the progress of the present invention, that is, according to the present invention, an aluminum alloy with high wear resistance can be prepared.
所述实施例为本发明的优选的实施方式,但本发明并不限于上述实施方式,在不背离本发明的实质内容的情况下,本领域技术人员能够做出的任何显而易见的改进、替换或变型均属于本发明的保护范围。The embodiments are preferred embodiments of the present invention, but the present invention is not limited to the above-mentioned embodiments, and any obvious improvement, replacement or All modifications belong to the protection scope of the present invention.
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