CN108728707A - A kind of crushing failure at high speed high-strength wrought magnesium alloys and preparation method thereof - Google Patents
A kind of crushing failure at high speed high-strength wrought magnesium alloys and preparation method thereof Download PDFInfo
- Publication number
- CN108728707A CN108728707A CN201810673189.9A CN201810673189A CN108728707A CN 108728707 A CN108728707 A CN 108728707A CN 201810673189 A CN201810673189 A CN 201810673189A CN 108728707 A CN108728707 A CN 108728707A
- Authority
- CN
- China
- Prior art keywords
- alloy
- high speed
- magnesium alloys
- preparation
- wrought magnesium
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Pending
Links
- 229910000861 Mg alloy Inorganic materials 0.000 title claims abstract description 31
- 238000002360 preparation method Methods 0.000 title claims abstract description 14
- 238000001125 extrusion Methods 0.000 claims abstract description 32
- 239000010949 copper Substances 0.000 claims abstract description 31
- 229910052802 copper Inorganic materials 0.000 claims abstract description 24
- 239000011777 magnesium Substances 0.000 claims abstract description 21
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 claims abstract description 15
- 229910052782 aluminium Inorganic materials 0.000 claims abstract description 14
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 claims abstract description 13
- 229910052749 magnesium Inorganic materials 0.000 claims abstract description 13
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 claims abstract description 12
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 claims abstract description 12
- 229910018182 Al—Cu Inorganic materials 0.000 claims abstract description 5
- 239000012535 impurity Substances 0.000 claims abstract description 3
- 239000000956 alloy Substances 0.000 claims description 55
- 229910045601 alloy Inorganic materials 0.000 claims description 54
- 239000002994 raw material Substances 0.000 claims description 23
- CPLXHLVBOLITMK-UHFFFAOYSA-N Magnesium oxide Chemical compound [Mg]=O CPLXHLVBOLITMK-UHFFFAOYSA-N 0.000 claims description 14
- 239000007788 liquid Substances 0.000 claims description 13
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 9
- 239000011812 mixed powder Substances 0.000 claims description 9
- OWXLRKWPEIAGAT-UHFFFAOYSA-N [Mg].[Cu] Chemical compound [Mg].[Cu] OWXLRKWPEIAGAT-UHFFFAOYSA-N 0.000 claims description 8
- 239000000395 magnesium oxide Substances 0.000 claims description 8
- 238000000034 method Methods 0.000 claims description 8
- 239000004698 Polyethylene Substances 0.000 claims description 7
- 238000005275 alloying Methods 0.000 claims description 7
- -1 polyethylene Polymers 0.000 claims description 7
- 229920000573 polyethylene Polymers 0.000 claims description 7
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 7
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 claims description 6
- 238000010791 quenching Methods 0.000 claims description 6
- 238000000265 homogenisation Methods 0.000 claims description 5
- 238000004321 preservation Methods 0.000 claims description 5
- 230000000171 quenching effect Effects 0.000 claims description 5
- 238000011282 treatment Methods 0.000 claims description 5
- 239000000314 lubricant Substances 0.000 claims description 4
- 230000001681 protective effect Effects 0.000 claims description 3
- 238000010438 heat treatment Methods 0.000 claims description 2
- 238000002844 melting Methods 0.000 claims description 2
- 230000008018 melting Effects 0.000 claims description 2
- 238000005507 spraying Methods 0.000 claims description 2
- 239000004411 aluminium Substances 0.000 claims 3
- 238000005266 casting Methods 0.000 claims 3
- 239000011248 coating agent Substances 0.000 claims 2
- 238000000576 coating method Methods 0.000 claims 2
- 229910000838 Al alloy Inorganic materials 0.000 claims 1
- 235000019441 ethanol Nutrition 0.000 claims 1
- 125000005909 ethyl alcohol group Chemical group 0.000 claims 1
- 238000010422 painting Methods 0.000 claims 1
- 239000000843 powder Substances 0.000 claims 1
- 238000010792 warming Methods 0.000 claims 1
- 238000012545 processing Methods 0.000 abstract description 4
- 238000005516 engineering process Methods 0.000 abstract description 3
- 230000007547 defect Effects 0.000 abstract description 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 12
- 239000000155 melt Substances 0.000 description 10
- 229910052742 iron Inorganic materials 0.000 description 6
- 239000007921 spray Substances 0.000 description 6
- 238000003756 stirring Methods 0.000 description 6
- 230000000052 comparative effect Effects 0.000 description 5
- 238000012986 modification Methods 0.000 description 3
- 230000004048 modification Effects 0.000 description 3
- 229910052761 rare earth metal Inorganic materials 0.000 description 3
- 229910019021 Mg 2 Sn Inorganic materials 0.000 description 2
- 229910003023 Mg-Al Inorganic materials 0.000 description 2
- 229910019074 Mg-Sn Inorganic materials 0.000 description 2
- 229910019382 Mg—Sn Inorganic materials 0.000 description 2
- 238000010586 diagram Methods 0.000 description 2
- AXZKOIWUVFPNLO-UHFFFAOYSA-N magnesium;oxygen(2-) Chemical compound [O-2].[Mg+2] AXZKOIWUVFPNLO-UHFFFAOYSA-N 0.000 description 2
- TWNQGVIAIRXVLR-UHFFFAOYSA-N oxo(oxoalumanyloxy)alumane Chemical compound O=[Al]O[Al]=O TWNQGVIAIRXVLR-UHFFFAOYSA-N 0.000 description 2
- 239000003973 paint Substances 0.000 description 2
- 150000002910 rare earth metals Chemical class 0.000 description 2
- 239000000243 solution Substances 0.000 description 2
- 238000005728 strengthening Methods 0.000 description 2
- 229910019086 Mg-Cu Inorganic materials 0.000 description 1
- 229910000691 Re alloy Inorganic materials 0.000 description 1
- 238000003723 Smelting Methods 0.000 description 1
- 229910018725 Sn—Al Inorganic materials 0.000 description 1
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- 238000005336 cracking Methods 0.000 description 1
- 230000007812 deficiency Effects 0.000 description 1
- 238000004090 dissolution Methods 0.000 description 1
- 230000009977 dual effect Effects 0.000 description 1
- 238000001192 hot extrusion Methods 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 239000007769 metal material Substances 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 238000011017 operating method Methods 0.000 description 1
- 239000011148 porous material Substances 0.000 description 1
- 238000012827 research and development Methods 0.000 description 1
- 230000035939 shock Effects 0.000 description 1
- 239000002893 slag Substances 0.000 description 1
- 239000006104 solid solution Substances 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C23/00—Alloys based on magnesium
-
- 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
- C22C1/02—Making non-ferrous alloys by melting
- C22C1/03—Making non-ferrous alloys by melting using master alloys
-
- 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
- C22F1/008—Using a protective surface layer
-
- 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
- C22F1/06—Changing the physical structure of non-ferrous metals or alloys by heat treatment or by hot or cold working of magnesium or alloys based thereon
Landscapes
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Mechanical Engineering (AREA)
- Metallurgy (AREA)
- Organic Chemistry (AREA)
- Physics & Mathematics (AREA)
- Thermal Sciences (AREA)
- Crystallography & Structural Chemistry (AREA)
- Extrusion Of Metal (AREA)
- Powder Metallurgy (AREA)
Abstract
本发明公开了一种快速挤压高强度变形镁合金,是由以下质量百分比的组分组成:工业纯锡:5%~7%;工业纯铝:1%~2%;铜:0.1%~3%;其余为工业纯镁和微量杂质元素;本发明还提供了高强度变形镁合金制备方法,采用快速挤压方法,操作简单、方便,便于推广应用。本发明通过快速挤压方法制备的Mg‑Sn‑Al‑Cu变形镁合金,在具有较高的强度的同时仍保持较好的延伸率,解决了现有的镁合金挤压加工制备方法中无法采用快速挤压工艺,型材缺陷多等问题,使其加工效率和成品率得以提高。
The invention discloses a rapidly extruded high-strength deformed magnesium alloy, which is composed of the following components by mass percentage: industrial pure tin: 5%~7%; industrial pure aluminum: 1%~2%; copper: 0.1%~ 3%; the rest is industrial pure magnesium and trace impurity elements; the invention also provides a preparation method of high-strength wrought magnesium alloy, which adopts a rapid extrusion method, is simple and convenient to operate, and is convenient for popularization and application. The Mg-Sn-Al-Cu deformed magnesium alloy prepared by the rapid extrusion method in the present invention has high strength while still maintaining a good elongation, which solves the problem that cannot be solved in the existing magnesium alloy extrusion processing preparation method. The use of rapid extrusion technology, many defects in the profile, etc., improve the processing efficiency and yield.
Description
技术领域technical field
本发明涉及金属材料领域,特别是涉及一种无稀土的含铜的高强度变形镁合金及其制备方法。The invention relates to the field of metal materials, in particular to a rare-earth-free high-strength wrought magnesium alloy containing copper and a preparation method thereof.
背景技术Background technique
镁合金具有密度小、比刚度和比强度高、优越的减震性能、良好的机械性能、等一系列优点,是很有前景的轻质结构材料之一。目前得到广泛应用的镁合金合金化元素包括有铝,锌,稀土等。这些合金的综合性能提高的同时,也有一定的局限行。其中Mg-Al合金的高温应用受到限制,Mg-Zn-RE合金具有优异的力学性能和较好的高温服役能力,但是稀土元素高昂的价格和日渐稀缺的储量限制其在民用领域的大规模应用和推广。因此,为推广镁合金材料的应用,研发新型不含稀土的轻质高强镁合金的需求日益增加。在这样的背景下,Mg-Sn合金愈发受到了研究者们的关注。此外,针对目前应用广泛的Mg-Al系挤压合金无法采用快速挤压工艺的缺点,Mg-Sn系变形镁合金中的Mg2Sn相具有较高的熔点,在高速挤压的过程中并不会发生第二相溶解而导致合金型材变形开裂。Magnesium alloy has a series of advantages such as low density, high specific stiffness and specific strength, superior shock absorption performance, good mechanical properties, etc., and is one of the promising lightweight structural materials. Alloying elements of magnesium alloys widely used at present include aluminum, zinc, rare earth and so on. While the comprehensive properties of these alloys are improved, they also have certain limitations. Among them, the high-temperature application of Mg-Al alloy is limited, and Mg-Zn-RE alloy has excellent mechanical properties and good high-temperature service ability, but the high price and increasingly scarce reserves of rare earth elements limit its large-scale application in the civil field. and promotion. Therefore, in order to promote the application of magnesium alloy materials, the demand for research and development of new lightweight high-strength magnesium alloys that do not contain rare earths is increasing. In this context, Mg-Sn alloys have attracted more and more attention from researchers. In addition, in view of the disadvantage that the currently widely used Mg-Al series extrusion alloy cannot adopt the rapid extrusion process, the Mg 2 Sn phase in the Mg-Sn series wrought magnesium alloy has a relatively high melting point, and is not formed during the high-speed extrusion process. There will be no second phase dissolution to cause deformation and cracking of the alloy profile.
发明内容Contents of the invention
针对上述的不足,本发明提供了快速挤压高强度变形镁合金及其制备方法,本发明是通过以下技术方案实现的:In view of the above-mentioned deficiencies, the present invention provides rapid extruding high-strength deformed magnesium alloys and a preparation method thereof, and the present invention is achieved through the following technical solutions:
一种快速挤压高强度变形镁合金,该合金为Mg-Sn-Al-Cu变形镁合金,原料组分及质量百分含量如下:A rapidly extruded high-strength deformed magnesium alloy, the alloy is a Mg-Sn-Al-Cu deformed magnesium alloy, and the raw material components and mass percentages are as follows:
工业纯锡:5%~7%;工业纯铝:1%~2%;铜(以铜的质量分数计量):0.1%~3%;余量为工业纯镁和微量杂质元素;制备所用的工业纯镁、工业纯铝以及工业纯锡纯度都在99%以上。Industrial pure tin: 5%~7%; industrial pure aluminum: 1%~2%; copper (measured by the mass fraction of copper): 0.1%~3%; the balance is industrial pure magnesium and trace impurity elements; The purity of industrial pure magnesium, industrial pure aluminum and industrial pure tin is above 99%.
优选地,铜是以铜的质量分数计量,添加时以Mg-30wt.%Cu中间合金的形式添加。Preferably, copper is measured by the mass fraction of copper, and is added in the form of Mg-30wt.%Cu master alloy.
上述所述的一种快速挤压高强度变形镁合金的制备方法,按照下述步骤进行:The preparation method of a kind of rapid extrusion high-strength deformed magnesium alloy described above is carried out according to the following steps:
(1)清理干净合金化坩埚,将其预热至250℃-300℃,将所用原料预热至80℃-100℃,通入保护气体,将工业纯镁和工业纯锡投入合金化坩埚在710℃-730℃的温度范围内融化成合金液体;(1) Clean up the alloying crucible, preheat it to 250°C-300°C, preheat the raw materials used to 80°C-100°C, pass in protective gas, put industrial pure magnesium and industrial pure tin into the alloying crucible Melt into alloy liquid within the temperature range of 710°C-730°C;
(2)按原料配比,在步骤(1)中得到的合金液体中加入工业纯铝和镁铜中间合金,在710℃-730℃的温度范围内融化成合金液体;(2) According to the ratio of raw materials, industrial pure aluminum and magnesium-copper master alloy are added to the alloy liquid obtained in step (1), and the alloy liquid is melted in the temperature range of 710°C-730°C;
(3)将在步骤(2)中得到的合金液体,在700℃-720℃静置30-40分钟,并充分搅拌1-3分钟,打掉表面的浮渣和氧化皮,得到合金液体;(3) Let the alloy liquid obtained in step (2) stand at 700°C-720°C for 30-40 minutes, and fully stir for 1-3 minutes to remove the scum and scale on the surface to obtain the alloy liquid;
(4)随后取出合金液体冷却至700℃,在气体保护的条件下将步骤(3)中得到的合金液体,浇注至预热到150℃-200℃的铁模中,制备出铸锭;(4) Then take out the alloy liquid and cool it to 700°C, and pour the alloy liquid obtained in step (3) into an iron mold preheated to 150°C-200°C under the condition of gas protection to prepare an ingot;
(5)均匀化处理:将步骤(4)所制备的铸锭表面均匀喷涂涂料,在300℃-330℃的条件下保温8-10小时,经1小时升温到450℃-500℃,保温12-14小时,然后水淬,得到均匀化处理的试样;(5) Homogenization treatment: evenly spray paint on the surface of the ingot prepared in step (4), keep it warm for 8-10 hours at 300°C-330°C, heat it up to 450°C-500°C in 1 hour, and keep it warm for 12 -14 hours, then quenched in water to obtain a homogenized sample;
(6)挤压:将步骤(5)所均匀化处理后得到的镁合金铸锭,车皮之后放入电阻炉中在300℃~350℃下预热2小时,在模具型腔和顶杆涂覆上润滑剂,在300~400℃下放入挤压机进行挤压成型,即可得到高强度变形镁合金。(6) Extrusion: cast the magnesium alloy ingot obtained after the homogenization treatment in step (5), put it into a resistance furnace after the car body, and preheat it at 300°C~350°C for 2 hours, and coat the mold cavity and ejector pin Cover it with lubricant, put it into an extruder at 300~400°C for extrusion molding, and then you can get a high-strength deformed magnesium alloy.
优选地,在熔炼过程中通入的保护气为SF6和CO2混合气体,体积比例为1:100。Preferably, the protective gas introduced during the smelting process is a mixed gas of SF 6 and CO 2 with a volume ratio of 1:100.
优选地,铸锭表面喷涂的涂料为氧化镁和氧化铝混合粉末,质量比例为3:1,采用无水乙醇混合,每10g混合粉末配用45-50ml无水乙醇。Preferably, the paint sprayed on the surface of the ingot is a mixed powder of magnesium oxide and aluminum oxide with a mass ratio of 3:1, mixed with absolute ethanol, and 45-50 ml of absolute ethanol is used for every 10 g of the mixed powder.
优选地,模具型腔和顶杆所涂覆的润滑剂为聚乙烯蜡。Preferably, the lubricant coated on the mold cavity and ejector pin is polyethylene wax.
优选地,采用直接加热快速挤压工艺,挤压比为30:1,挤压速度为6~10m/ min。Preferably, the direct heating rapid extrusion process is adopted, the extrusion ratio is 30:1, and the extrusion speed is 6-10m/min.
附图说明Description of drawings
图1:实施例2制备的挤压合金金相图。Figure 1: Metallographic diagram of the extruded alloy prepared in Example 2.
图2:对比例1制备的挤压合金金相图。Figure 2: Metallographic diagram of the extruded alloy prepared in Comparative Example 1.
图3:对比例3制备的预挤压铸锭车皮后的表面宏观形貌图片。Fig. 3: A picture of the surface macroscopic appearance of the pre-extruded ingot car skin prepared in Comparative Example 3.
有益效果Beneficial effect
1.本发明所提出的Mg-Sn-Al-Cu合金是一种新型无稀土的含铜镁合金,采用的合金化元素都是价格低廉的金属。在Mg-Sn-Al三元体系中,只有Mg17Al12,Mg2Sn和α-Mg三相,添加Cu后还形成了Mg-Cu相和Al-Cu相,因此合金化元素的添加对合金起到固溶强化和第二相强化的双重结果。经过热挤压后制备出具有较高强度的镁合金型材。1. The Mg-Sn-Al-Cu alloy proposed by the present invention is a novel rare earth-free copper-magnesium alloy, and the alloying elements used are all cheap metals. In the Mg-Sn-Al ternary system, there are only three phases of Mg 17 Al 12 , Mg 2 Sn and α-Mg, and Mg-Cu phase and Al-Cu phase are also formed after adding Cu, so the addition of alloying elements has a great influence on The alloy plays a dual role of solid solution strengthening and second phase strengthening. After hot extrusion, a magnesium alloy profile with high strength is prepared.
2.本发明采用较为简单的快速挤压的加工工艺,通过合理调控预热温度和挤压温度,实现快速、大挤压比挤压加工,挤压速度最高可达10m/min,平均挤压比30:1,挤压型材表面平整光洁,没有明显的缺陷和裂纹,致密度高。所获得的挤压合金强度超过大部分的AZ系列变形镁合金,与商用的稀土变形镁合金WE54相当。2. The present invention adopts a relatively simple rapid extrusion processing technology, and realizes rapid extrusion processing with a large extrusion ratio by reasonably adjusting the preheating temperature and extrusion temperature. The extrusion speed can reach up to 10m/min, and the average extrusion The ratio is 30:1, the surface of the extruded profile is smooth and clean, without obvious defects and cracks, and the density is high. The strength of the extruded alloy obtained exceeds most of the AZ series wrought magnesium alloys, and is comparable to the commercial rare earth wrought magnesium alloy WE54.
具体实施方式Detailed ways
下面对本发明的实施例作详细说明,本实施例在以本发明技术方案为前提下进行实施,给出了详细的实施方式和具体的操作过程,但本发明的保护范围不限于下述的实施例。The embodiments of the present invention are described in detail below. This embodiment is implemented on the premise of the technical solution of the present invention, and detailed implementation methods and specific operating procedures are provided, but the protection scope of the present invention is not limited to the following implementation example.
实施例1Example 1
(1)按照质量百分比称取合金原料:Sn:6%;Al:1%;Cu:0.5%(以纯铜的质量分数计量,以Mg-30wt.%Cu中间合金的形式添加);余量为Mg。(1) Weigh the alloy raw materials according to the mass percentage: Sn: 6%; Al: 1%; Cu: 0.5% (measured by the mass fraction of pure copper, added in the form of Mg-30wt.%Cu master alloy); the balance is Mg.
(2)清理干净合金化坩埚,将其预热至250℃-300℃,将所用原料预热至80℃-100℃,体积比为1:100的SF6和CO2混合气体保护下,先对工业纯镁和工业纯锡在710℃-730℃的温度范围内进行熔炼,待全部融化后,加入的工业纯铝和镁铜中间合金,待原料完全融化后将熔体在720℃静置35分钟,并充分搅拌1-3分钟,打掉表面的浮渣和氧化皮。随后取出熔体冷却至700℃,在气体保护的条件下浇注至预热到150℃-200℃的铁模中,制备出铸锭。(2) Clean up the alloyed crucible, preheat it to 250°C-300°C, and preheat the raw materials to 80°C-100°C, under the protection of a mixed gas of SF 6 and CO 2 with a volume ratio of 1:100, first Melt industrial pure magnesium and industrial pure tin at a temperature range of 710°C-730°C. After they are completely melted, add industrial pure aluminum and magnesium-copper master alloy. After the raw materials are completely melted, let the melt stand at 720°C 35 minutes, and fully stir for 1-3 minutes to remove the scum and scale on the surface. Then take out the melt and cool it to 700°C, pour it into an iron mold preheated to 150°C-200°C under the condition of gas protection, and prepare an ingot.
(3)将所制备的铸锭表面均匀喷涂上采用无水乙醇混合的质量比为3:1的氧化镁和氧化铝的混合粉末,在330℃的条件下保温10小时后,经1小时升温到450℃,保温12小时,然后水淬,得到均匀化处理的试样;(3) Evenly spray the surface of the prepared ingot with the mixed powder of magnesia and alumina mixed with anhydrous ethanol at a mass ratio of 3:1, heat it at 330°C for 10 hours, and then heat it up for 1 hour Heat at 450°C for 12 hours, then quench in water to obtain a homogenized sample;
(4)将均匀化处理后的铸锭,车皮之后在350℃下预热2小时,在模具型腔和顶杆涂覆上聚乙烯蜡,在400℃下进行挤压;挤压比为30:1,挤压速度为6m/min,制备出挤压型材,该合金抗拉强度为300.1MPa,延伸率为7.42%。(4) Preheat the homogenized ingot and wagon at 350°C for 2 hours, coat the mold cavity and ejector pin with polyethylene wax, and extrude at 400°C; the extrusion ratio is 30 : 1, the extrusion speed is 6m/min, and an extruded profile is prepared. The tensile strength of the alloy is 300.1MPa, and the elongation is 7.42%.
实施例2Example 2
(1)按照质量百分比称取合金原料:Sn:6%;Al:1%;Cu:1%(以纯铜的质量分数计量,以Mg-30wt.%Cu中间合金的形式添加);余量为Mg。(1) Weigh the alloy raw materials according to the mass percentage: Sn: 6%; Al: 1%; Cu: 1% (measured by the mass fraction of pure copper, added in the form of Mg-30wt.%Cu master alloy); the balance is Mg.
(2)清理干净合金化坩埚,将其预热至250℃-300℃,将所用原料预热至80℃-100℃,体积比为1:100的SF6和CO2混合气体保护下,先对工业纯镁和工业纯锡在710℃-730℃的温度范围内进行熔炼,待全部融化后,加入的工业纯铝和镁铜中间合金,待原料完全融化后将熔体在720℃静置35分钟,并充分搅拌1-3分钟,打掉表面的浮渣和氧化皮。随后取出熔体冷却至700℃,在气体保护的条件下浇注至预热到150℃-200℃的铁模中,制备出铸锭。(2) Clean up the alloyed crucible, preheat it to 250°C-300°C, and preheat the raw materials to 80°C-100°C, under the protection of a mixed gas of SF 6 and CO 2 with a volume ratio of 1:100, first Melt industrial pure magnesium and industrial pure tin at a temperature range of 710°C-730°C. After they are completely melted, add industrial pure aluminum and magnesium-copper master alloy. After the raw materials are completely melted, let the melt stand at 720°C 35 minutes, and fully stir for 1-3 minutes to remove the scum and scale on the surface. Then take out the melt and cool it to 700°C, pour it into an iron mold preheated to 150°C-200°C under the condition of gas protection, and prepare an ingot.
(3)将所制备的铸锭表面均匀喷涂采用无水乙醇混合的质量比为3:1的氧化镁和氧化铝的混合粉末,在330℃的条件下保温10小时后,经1小时升温到450℃,保温12小时,然后水淬,得到均匀化处理的试样;(3) Evenly spray the surface of the prepared ingot with the mixed powder of magnesia and alumina mixed with absolute ethanol at a mass ratio of 3:1, keep it at 330°C for 10 hours, and then heat it up to 450°C, heat preservation for 12 hours, and then water quenching to obtain a homogenized sample;
(4)将均匀化处理后的铸锭,车皮之后在350℃下预热2小时,在模具型腔和顶杆涂覆上聚乙烯蜡,在400℃下进行挤压;挤压比为30:1,挤压速度为8m/min,制备出挤压型材。该合金抗拉强度为310MPa,延伸率为6.60%。(4) Preheat the homogenized ingot and wagon at 350°C for 2 hours, coat the mold cavity and ejector pin with polyethylene wax, and extrude at 400°C; the extrusion ratio is 30 : 1, the extrusion speed is 8m/min, and an extruded profile is prepared. The alloy has a tensile strength of 310MPa and an elongation of 6.60%.
实施例3Example 3
(1)按照质量百分比称取合金原料:Sn:6%;Al:1%;Cu:2%(以纯铜的质量分数计量,以Mg-30wt.%Cu中间合金的形式添加);余量为Mg。(1) Weigh the alloy raw materials according to the mass percentage: Sn: 6%; Al: 1%; Cu: 2% (measured by the mass fraction of pure copper, added in the form of Mg-30wt.%Cu master alloy); the balance is Mg.
(2)清理干净合金化坩埚,将其预热至250℃-300℃,将所用原料预热至80℃-100℃,体积比为1:100的SF6和CO2混合气体保护下,先对工业纯镁和工业纯锡在710℃-730℃的温度范围内进行熔炼,待全部融化后,加入的工业纯铝和镁铜中间合金,待原料完全融化后将熔体在720℃静置35分钟,并充分搅拌1-3分钟,打掉表面的浮渣和氧化皮。随后取出熔体冷却至700℃,在气体保护的条件下浇注至预热到150℃-200℃的铁模中,制备出铸锭。(2) Clean up the alloyed crucible, preheat it to 250°C-300°C, and preheat the raw materials to 80°C-100°C, under the protection of a mixed gas of SF 6 and CO 2 with a volume ratio of 1:100, first Melt industrial pure magnesium and industrial pure tin at a temperature range of 710°C-730°C. After they are completely melted, add industrial pure aluminum and magnesium-copper master alloy. After the raw materials are completely melted, let the melt stand at 720°C 35 minutes, and fully stir for 1-3 minutes to remove the scum and scale on the surface. Then take out the melt and cool it to 700°C, pour it into an iron mold preheated to 150°C-200°C under the condition of gas protection, and prepare an ingot.
(3)将所制备的铸锭表面均匀喷涂采用无水乙醇混合的质量比为3:1的氧化镁和氧化铝的混合粉末,在330℃的条件下保温10小时后,经1小时升温到480℃,保温12小时,然后水淬,得到均匀化处理的试样;(3) Evenly spray the surface of the prepared ingot with the mixed powder of magnesia and alumina mixed with absolute ethanol at a mass ratio of 3:1, keep it at 330°C for 10 hours, and then heat it up to 480°C, heat preservation for 12 hours, and then water quenching to obtain a homogenized sample;
(4)将均匀化处理后的铸锭,车皮之后在350℃下预热2小时,在模具型腔和顶杆涂覆上聚乙烯蜡,在400℃下进行挤压;挤压比为30:1,挤压速度为8m/min,制备出挤压型材。该合金抗拉强度为282.6MPa,延伸率为7.20%。(4) Preheat the homogenized ingot and wagon at 350°C for 2 hours, coat the mold cavity and ejector pin with polyethylene wax, and extrude at 400°C; the extrusion ratio is 30 : 1, the extrusion speed is 8m/min, and an extruded profile is prepared. The alloy has a tensile strength of 282.6MPa and an elongation of 7.20%.
实施例4Example 4
(1)按照质量百分比称取合金原料:Sn:6%;Al:1.5%;Cu:1%(以纯铜的质量分数计量,以Mg-30wt.%Cu中间合金的形式添加);余量为Mg。(1) Weigh the alloy raw materials according to the mass percentage: Sn: 6%; Al: 1.5%; Cu: 1% (measured by the mass fraction of pure copper, added in the form of Mg-30wt.%Cu master alloy); the balance is Mg.
(2)清理干净合金化坩埚,将其预热至250℃-300℃,将所用原料预热至80℃-100℃,体积比为1:100的SF6和CO2混合气体保护下,先对工业纯镁和工业纯锡在710℃-730℃的温度范围内进行熔炼,待全部融化后,加入的工业纯铝和镁铜中间合金,待原料完全融化后将熔体在720℃静置35分钟,并充分搅拌1-3分钟,打掉表面的浮渣和氧化皮。随后取出熔体冷却至700℃,在气体保护的条件下浇注至预热到150℃-200℃的铁模中,制备出铸锭。(2) Clean up the alloyed crucible, preheat it to 250°C-300°C, and preheat the raw materials to 80°C-100°C, under the protection of a mixed gas of SF 6 and CO 2 with a volume ratio of 1:100, first Melt industrial pure magnesium and industrial pure tin at a temperature range of 710°C-730°C. After they are completely melted, add industrial pure aluminum and magnesium-copper master alloy. After the raw materials are completely melted, let the melt stand at 720°C 35 minutes, and fully stir for 1-3 minutes to remove the scum and scale on the surface. Then take out the melt and cool it to 700°C, pour it into an iron mold preheated to 150°C-200°C under the condition of gas protection, and prepare an ingot.
(3)将所制备的铸锭表面均匀喷涂采用无水乙醇混合的质量比为3:1的氧化镁和氧化铝的混合粉末,在330℃的条件下保温10小时后,经1小时升温到480℃,保温12小时,然后水淬,得到均匀化处理的试样;(3) Evenly spray the surface of the prepared ingot with the mixed powder of magnesia and alumina mixed with absolute ethanol at a mass ratio of 3:1, keep it at 330°C for 10 hours, and then heat it up to 480°C, heat preservation for 12 hours, and then water quenching to obtain a homogenized sample;
(4)将均匀化处理后的铸锭,车皮之后在350℃下预热2小时,在模具型腔和顶杆涂覆上聚乙烯蜡,在400℃下进行挤压;挤压比为30:1,挤压速度为10m/min,制备出挤压型材。该合金抗拉强度为298.5MPa,延伸率为7.18%。(4) Preheat the homogenized ingot and wagon at 350°C for 2 hours, coat the mold cavity and ejector pin with polyethylene wax, and extrude at 400°C; the extrusion ratio is 30 : 1, the extrusion speed is 10m/min, and an extruded profile is prepared. The alloy has a tensile strength of 298.5MPa and an elongation of 7.18%.
实施例5Example 5
(1)按照质量百分比称取合金原料:Sn:7%;Al:2%;Cu:1%(以纯铜的质量分数计量,以Mg-30wt.%Cu中间合金的形式添加);余量为Mg。(1) Weigh the alloy raw materials according to the mass percentage: Sn: 7%; Al: 2%; Cu: 1% (measured by the mass fraction of pure copper, added in the form of Mg-30wt.%Cu master alloy); the balance is Mg.
(2)清理干净合金化坩埚,将其预热至250℃-300℃,将所用原料预热至80℃-100℃,体积比为1:100的SF6和CO2混合气体保护下,先对工业纯镁和工业纯锡在710℃-730℃的温度范围内进行熔炼,待全部融化后,加入的工业纯铝和镁铜中间合金,待原料完全融化后将熔体在720℃静置35分钟,并充分搅拌1-3分钟,打掉表面的浮渣和氧化皮。随后取出熔体冷却至700℃,在气体保护的条件下浇注至预热到150℃-200℃的铁模中,制备出铸锭。(2) Clean up the alloyed crucible, preheat it to 250°C-300°C, and preheat the raw materials to 80°C-100°C, under the protection of a mixed gas of SF 6 and CO 2 with a volume ratio of 1:100, first Melt industrial pure magnesium and industrial pure tin at a temperature range of 710°C-730°C. After they are completely melted, add industrial pure aluminum and magnesium-copper master alloy. After the raw materials are completely melted, let the melt stand at 720°C 35 minutes, and fully stir for 1-3 minutes to remove the scum and scale on the surface. Then take out the melt and cool it to 700°C, pour it into an iron mold preheated to 150°C-200°C under the condition of gas protection, and prepare an ingot.
(3)将所制备的铸锭表面均匀喷涂采用无水乙醇混合的质量比为3:1的氧化镁和氧化铝的混合粉末,在330℃的条件下保温10小时后,经1小时升温到480℃,保温12小时,然后水淬,得到均匀化处理的试样;(3) Evenly spray the surface of the prepared ingot with the mixed powder of magnesia and alumina mixed with absolute ethanol at a mass ratio of 3:1, keep it at 330°C for 10 hours, and then heat it up to 480°C, heat preservation for 12 hours, and then water quenching to obtain a homogenized sample;
(4)将均匀化处理后的铸锭,车皮之后在350℃下预热2小时,在模具型腔和顶杆涂覆上聚乙烯蜡,在400℃下进行挤压;挤压比为30:1,挤压速度为10m/min,制备出挤压型材。该合金抗拉强度为283.0MPa,延伸率为6.88%。(4) Preheat the homogenized ingot and wagon at 350°C for 2 hours, coat the mold cavity and ejector pin with polyethylene wax, and extrude at 400°C; the extrusion ratio is 30 : 1, the extrusion speed is 10m/min, and an extruded profile is prepared. The alloy has a tensile strength of 283.0MPa and an elongation of 6.88%.
对比例1Comparative example 1
按照质量百分比称取合金原料:Sn:6%;Al:1%;Cu:1%(以纯铜的形式添加);余量为Mg。Alloy raw materials are weighed according to mass percentage: Sn: 6%; Al: 1%; Cu: 1% (added in the form of pure copper); the balance is Mg.
制备方法同实施例2。The preparation method is the same as in Example 2.
制备出的合金的抗拉强度为255.3MPa,延伸率为5.30%。The tensile strength of the prepared alloy is 255.3MPa, and the elongation is 5.30%.
对比例2Comparative example 2
按照质量百分比取:Sn:2.7%,Al:30.8%,Cu:1.9%(以纯铜的质量分数计量,以Mg-30wt.%Cu中间合金的形式添加);余量为Mg;According to the mass percentage: Sn: 2.7%, Al: 30.8%, Cu: 1.9% (measured by the mass fraction of pure copper, added in the form of Mg-30wt.%Cu master alloy); the balance is Mg;
制备方法同实施例2。The preparation method is the same as in Example 2.
制备出的合金的抗拉强度为193.7MPa,延伸率为3.50%。The tensile strength of the prepared alloy is 193.7MPa, and the elongation is 3.50%.
对比例3Comparative example 3
将实施例2中“步骤(3)将所制备的铸锭表面均匀喷涂采用无水乙醇混合的质量比为3:1的氧化镁和氧化铝的混合粉末”此步骤去除,其他按照实施例2所述的原料配比及其制备方法制备合金,所制备的合金的缺点为:预挤压铸锭表面出现黑色的氧化层以及较深的氧化烧损的蚀坑,车皮至相应尺寸仍有部分保留,挤压后的型材内部出现夹渣和气孔。其抗拉强度为268.5MPa,延伸率为4.36%。In Example 2, the step "step (3) evenly spraying the surface of the prepared ingot with the mixed powder of magnesium oxide and aluminum oxide mixed with absolute ethanol at a mass ratio of 3:1" was removed, and the others were as in Example 2 The alloy is prepared according to the ratio of raw materials and its preparation method. The disadvantages of the prepared alloy are: a black oxide layer and deep pits of oxidized burning appear on the surface of the pre-extruded ingot, and the car body still partially remains when it reaches the corresponding size. , Slag inclusions and pores appear inside the extruded profile. Its tensile strength is 268.5MPa and its elongation is 4.36%.
显然,本领域的技术人员可以对本发明进行各种改动和变型而不脱离本发明的精神和范围。这样,倘若本发明的这些修改和变型属于本发明权利要求及其等同技术的范围之内,则本发明也意图包含这些改动和变型在内。Obviously, those skilled in the art can make various changes and modifications to the present invention without departing from the spirit and scope of the present invention. Thus, if these modifications and variations of the present invention fall within the scope of the claims of the present invention and equivalent technologies thereof, the present invention also intends to include these modifications and variations.
Claims (7)
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN201810673189.9A CN108728707A (en) | 2018-06-27 | 2018-06-27 | A kind of crushing failure at high speed high-strength wrought magnesium alloys and preparation method thereof |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN201810673189.9A CN108728707A (en) | 2018-06-27 | 2018-06-27 | A kind of crushing failure at high speed high-strength wrought magnesium alloys and preparation method thereof |
Publications (1)
Publication Number | Publication Date |
---|---|
CN108728707A true CN108728707A (en) | 2018-11-02 |
Family
ID=63931009
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CN201810673189.9A Pending CN108728707A (en) | 2018-06-27 | 2018-06-27 | A kind of crushing failure at high speed high-strength wrought magnesium alloys and preparation method thereof |
Country Status (1)
Country | Link |
---|---|
CN (1) | CN108728707A (en) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN109518050A (en) * | 2018-12-18 | 2019-03-26 | 济南大学 | A kind of medium temperature crushing failure at high speed high-strength and high ductility wrought magnesium alloy and preparation method thereof |
CN110669967A (en) * | 2019-09-23 | 2020-01-10 | 山东南山铝业股份有限公司 | Rapid-extrusion high-strength wrought aluminum alloy and preparation method thereof |
CN110983128A (en) * | 2019-09-23 | 2020-04-10 | 山东南山铝业股份有限公司 | High-strength heat-resistant wrought aluminum alloy and preparation method thereof |
Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN103114231A (en) * | 2013-03-07 | 2013-05-22 | 重庆大学 | Mg-Sn-Al wrought magnesium alloy and preparation method thereof |
CN105603283A (en) * | 2016-03-31 | 2016-05-25 | 哈尔滨理工大学 | Method for preparing and forming high-strength high-toughness wrought magnesium alloy |
CN107326235A (en) * | 2017-07-20 | 2017-11-07 | 重庆大学 | A kind of high-strength Mg Zn Al series deformation magnesium alloys containing Cu and preparation method thereof |
-
2018
- 2018-06-27 CN CN201810673189.9A patent/CN108728707A/en active Pending
Patent Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN103114231A (en) * | 2013-03-07 | 2013-05-22 | 重庆大学 | Mg-Sn-Al wrought magnesium alloy and preparation method thereof |
CN105603283A (en) * | 2016-03-31 | 2016-05-25 | 哈尔滨理工大学 | Method for preparing and forming high-strength high-toughness wrought magnesium alloy |
CN107326235A (en) * | 2017-07-20 | 2017-11-07 | 重庆大学 | A kind of high-strength Mg Zn Al series deformation magnesium alloys containing Cu and preparation method thereof |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN109518050A (en) * | 2018-12-18 | 2019-03-26 | 济南大学 | A kind of medium temperature crushing failure at high speed high-strength and high ductility wrought magnesium alloy and preparation method thereof |
CN110669967A (en) * | 2019-09-23 | 2020-01-10 | 山东南山铝业股份有限公司 | Rapid-extrusion high-strength wrought aluminum alloy and preparation method thereof |
CN110983128A (en) * | 2019-09-23 | 2020-04-10 | 山东南山铝业股份有限公司 | High-strength heat-resistant wrought aluminum alloy and preparation method thereof |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
CN100432258C (en) | Quasi crystal phase fortified magnesium lithium alloy and its preparation method | |
CN101787472B (en) | Heat-resistant forged magnesium-rare earth alloy and preparation method thereof | |
CN105132772B (en) | Low-cost non-rare-earth type high-strength magnesium alloy and preparing method thereof | |
CN102766789B (en) | Preparation method of aluminum alloy | |
CN101407879A (en) | Yb-containing deformation magnesium alloy and dynamic precipitation strengthening-toughening preparation thereof | |
CN113737060B (en) | AlSiLi phase time-effect strengthened low-density aluminum alloy and preparation method thereof | |
CN103938045A (en) | Calcium-containing deforming magnesium alloy and preparation method of calcium-containing deforming magnesium alloy bar | |
CN104032195A (en) | Efficiently-extrudable low-cost high-performance heat-conducting magnesium alloy and preparation method thereof | |
WO2020155578A1 (en) | Low-alloy high-performance superplastic magnesium alloy and preparation method therefor | |
CN101871066A (en) | A kind of high-strength toughness magnesium alloy containing tin and zinc and preparation method thereof | |
CN103143582B (en) | A kind of aluminium alloy plate extrusion molding apparatus of high conductivity and technique | |
CN108728707A (en) | A kind of crushing failure at high speed high-strength wrought magnesium alloys and preparation method thereof | |
CN103498084A (en) | Novel high-strength high-conductivity aluminium-alloy conductor and production method thereof | |
CN106319314A (en) | High-speed extrusion high-strength deforming magnesium alloy and preparation method thereof | |
CN104498797A (en) | High-strength casting magnesium alloy with low hot cracking tendency and preparation method for high-strength casting magnesium alloy | |
CN101279361A (en) | A kind of preparation method of high strength and toughness magnesium alloy | |
CN101871068B (en) | A kind of high-strength high-plasticity magnesium alloy containing tin and aluminum and preparation method thereof | |
CN110643870A (en) | Corrosion-resistant high-performance wrought magnesium alloy and preparation method thereof | |
CN103659181A (en) | Preparation technology for aluminum alloy groove piece | |
CN103103398A (en) | A kind of smelting preparation method of anti-corrosion aluminum alloy profile | |
CN101805866B (en) | Deformed magnesium alloy for high-speed extrusion and preparation method thereof | |
CN104018049B (en) | A kind of superplastic magnesium alloy and preparation method thereof | |
CN102925775B (en) | Low-deformation-resistance wrought magnesium alloy and preparation method thereof | |
CN101824572B (en) | High-intensity and anti-corrosion Mg-Al-Zn-RE extruded magnesium alloy rich in Y-base rare earth alloy as well as production method and application thereof | |
CN108425052A (en) | A kind of heat-resistance high-strength wrought magnesium alloy and preparation method thereof |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
PB01 | Publication | ||
PB01 | Publication | ||
SE01 | Entry into force of request for substantive examination | ||
SE01 | Entry into force of request for substantive examination | ||
RJ01 | Rejection of invention patent application after publication | ||
RJ01 | Rejection of invention patent application after publication |
Application publication date: 20181102 |