CN116005039B - A kind of foamed aluminum and preparation method thereof - Google Patents
A kind of foamed aluminum and preparation method thereof Download PDFInfo
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- 229910052782 aluminium Inorganic materials 0.000 title claims abstract description 102
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 title claims abstract description 102
- 238000002360 preparation method Methods 0.000 title claims abstract description 11
- 230000003014 reinforcing effect Effects 0.000 claims abstract description 72
- 229910052751 metal Inorganic materials 0.000 claims abstract description 47
- 239000002184 metal Substances 0.000 claims abstract description 47
- 239000000843 powder Substances 0.000 claims abstract description 46
- 238000000034 method Methods 0.000 claims abstract description 36
- 238000005187 foaming Methods 0.000 claims abstract description 34
- 239000006260 foam Substances 0.000 claims abstract description 28
- 239000002994 raw material Substances 0.000 claims abstract description 25
- 238000004663 powder metallurgy Methods 0.000 claims abstract description 20
- 239000002243 precursor Substances 0.000 claims abstract description 18
- 239000002245 particle Substances 0.000 claims description 38
- 239000004088 foaming agent Substances 0.000 claims description 12
- 238000002156 mixing Methods 0.000 claims description 9
- 229920000049 Carbon (fiber) Polymers 0.000 claims description 8
- 239000004917 carbon fiber Substances 0.000 claims description 8
- 239000000919 ceramic Substances 0.000 claims description 7
- 239000010949 copper Substances 0.000 claims description 7
- KZHJGOXRZJKJNY-UHFFFAOYSA-N dioxosilane;oxo(oxoalumanyloxy)alumane Chemical compound O=[Si]=O.O=[Si]=O.O=[Al]O[Al]=O.O=[Al]O[Al]=O.O=[Al]O[Al]=O KZHJGOXRZJKJNY-UHFFFAOYSA-N 0.000 claims description 7
- 229910000765 intermetallic Inorganic materials 0.000 claims description 7
- 239000011777 magnesium Substances 0.000 claims description 7
- 229910052863 mullite Inorganic materials 0.000 claims description 7
- 239000000835 fiber Substances 0.000 claims description 6
- 229910052802 copper Inorganic materials 0.000 claims description 5
- 229910052749 magnesium Inorganic materials 0.000 claims description 5
- 229910052596 spinel Inorganic materials 0.000 claims description 5
- 239000011029 spinel Substances 0.000 claims description 5
- 239000011135 tin Substances 0.000 claims description 5
- 229910000048 titanium hydride Inorganic materials 0.000 claims description 5
- 229910000838 Al alloy Inorganic materials 0.000 claims description 4
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 claims description 4
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 claims description 4
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 claims description 4
- 229910045601 alloy Inorganic materials 0.000 claims description 4
- 239000000956 alloy Substances 0.000 claims description 4
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 claims description 3
- 229910052593 corundum Inorganic materials 0.000 claims description 3
- 229910052718 tin Inorganic materials 0.000 claims description 3
- -1 titanium hydride Chemical group 0.000 claims description 3
- 229910001845 yogo sapphire Inorganic materials 0.000 claims description 3
- AZDRQVAHHNSJOQ-UHFFFAOYSA-N alumane Chemical compound [AlH3] AZDRQVAHHNSJOQ-UHFFFAOYSA-N 0.000 claims description 2
- 238000002844 melting Methods 0.000 claims description 2
- 230000008018 melting Effects 0.000 claims description 2
- 238000007873 sieving Methods 0.000 claims description 2
- 239000011863 silicon-based powder Substances 0.000 claims description 2
- 239000011159 matrix material Substances 0.000 abstract description 24
- 230000008569 process Effects 0.000 abstract description 14
- 230000006835 compression Effects 0.000 abstract description 6
- 238000007906 compression Methods 0.000 abstract description 6
- 238000004519 manufacturing process Methods 0.000 abstract description 4
- 238000003825 pressing Methods 0.000 abstract description 2
- 230000002787 reinforcement Effects 0.000 description 27
- 230000006872 improvement Effects 0.000 description 12
- 239000000463 material Substances 0.000 description 6
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 6
- 101001121408 Homo sapiens L-amino-acid oxidase Proteins 0.000 description 5
- 102100026388 L-amino-acid oxidase Human genes 0.000 description 5
- 239000000203 mixture Substances 0.000 description 5
- 239000011248 coating agent Substances 0.000 description 4
- 238000000576 coating method Methods 0.000 description 4
- 239000002131 composite material Substances 0.000 description 4
- 230000000694 effects Effects 0.000 description 4
- 239000011148 porous material Substances 0.000 description 4
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 3
- 238000010521 absorption reaction Methods 0.000 description 3
- 239000006261 foam material Substances 0.000 description 3
- 239000002923 metal particle Substances 0.000 description 3
- 238000007747 plating Methods 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- 229910018072 Al 2 O 3 Inorganic materials 0.000 description 2
- 239000004484 Briquette Substances 0.000 description 2
- 230000009286 beneficial effect Effects 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 239000002041 carbon nanotube Substances 0.000 description 2
- 229910021393 carbon nanotube Inorganic materials 0.000 description 2
- 230000008021 deposition Effects 0.000 description 2
- 238000009826 distribution Methods 0.000 description 2
- 238000009713 electroplating Methods 0.000 description 2
- 238000011065 in-situ storage Methods 0.000 description 2
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- 101000827703 Homo sapiens Polyphosphoinositide phosphatase Proteins 0.000 description 1
- 102100023591 Polyphosphoinositide phosphatase Human genes 0.000 description 1
- 101100012902 Saccharomyces cerevisiae (strain ATCC 204508 / S288c) FIG2 gene Proteins 0.000 description 1
- 101100233916 Saccharomyces cerevisiae (strain ATCC 204508 / S288c) KAR5 gene Proteins 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
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- 229910052799 carbon Inorganic materials 0.000 description 1
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- 238000006243 chemical reaction Methods 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 239000002360 explosive Substances 0.000 description 1
- 239000011888 foil Substances 0.000 description 1
- 230000036541 health Effects 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 229910001385 heavy metal Inorganic materials 0.000 description 1
- 238000009775 high-speed stirring Methods 0.000 description 1
- 238000009776 industrial production Methods 0.000 description 1
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Abstract
Description
技术领域Technical Field
本发明属于泡沫铝制造技术领域,更具体地说,涉及一种泡沫铝及其制备方法。The invention belongs to the technical field of foam aluminum manufacturing, and more specifically, relates to foam aluminum and a preparation method thereof.
背景技术Background Art
泡沫铝是一种多孔结构功能一体化材料,集轻质、吸能、减震、缓冲、隔音、隔热、电磁屏蔽等多种优异功能于一身,满足系统减重、结构承载和多功能综合需求,在未来航空航天、汽车制造、轨道交通等领域具有广阔的开发及应用前景。Foam aluminum is a porous structural functional integrated material that integrates multiple excellent functions such as light weight, energy absorption, shock absorption, cushioning, sound insulation, heat insulation, electromagnetic shielding, etc. It meets the system's weight reduction, structural load-bearing and multi-functional comprehensive needs, and has broad development and application prospects in the future aerospace, automobile manufacturing, rail transit and other fields.
提高泡沫铝压缩强度是扩大泡沫铝应用的重要途径之一,粉末冶金法制备泡沫铝的发泡时间一般较短,很难通过控制基体成分组成,实现在短暂的发泡过程中原位自生成增强相,因此,目前主要通过外加增强相来提升泡沫铝材料的力学性能。增强相主要有陶瓷颗粒、晶须与短纤维等,同原位反应自生成的增强相相比,外加增强相在与基体的化学相容性及润湿性方面表现更差,导致增强效果不佳。在熔体发泡法制备泡沫铝过程中,虽然增强相作为第二相外加,但增强相与基体之间通过固-液结合,结合界面具有较好的润湿性;相比之下,粉末冶金法制备泡沫铝时外加的增强相只能与基体通过固-固物理结合,润湿性较差。但粉末冶金法在制备泡沫铝填充件及异形件上优势突出,为扩大优势,通过提升外加增强相与泡沫铝基体润湿性来提高其力学性能是值得研究的重要创新点。虽然有研究报道通过在增强相外表面镀金属来改善其与基体的润湿性能,但操作过程较为复杂。Improving the compressive strength of aluminum foam is one of the important ways to expand the application of aluminum foam. The foaming time of aluminum foam prepared by powder metallurgy is generally short, and it is difficult to achieve in-situ self-generation of reinforcing phases in a short foaming process by controlling the composition of the matrix. Therefore, the mechanical properties of aluminum foam materials are currently mainly improved by adding reinforcing phases. The reinforcing phases mainly include ceramic particles, whiskers and short fibers. Compared with the reinforcing phases generated by in-situ reactions, the added reinforcing phases have worse chemical compatibility and wettability with the matrix, resulting in poor reinforcement effect. In the process of preparing aluminum foam by melt foaming, although the reinforcing phase is added as the second phase, the reinforcing phase and the matrix are combined through solid-liquid bonding, and the bonding interface has good wettability; in contrast, when preparing aluminum foam by powder metallurgy, the added reinforcing phase can only be physically combined with the matrix through solid-solid bonding, and the wettability is poor. However, the powder metallurgy method has outstanding advantages in the preparation of aluminum foam fillings and special-shaped parts. In order to expand the advantages, it is an important innovation point worthy of research to improve its mechanical properties by improving the wettability of the added reinforcing phase and the aluminum foam matrix. Although some studies have reported that the wetting performance between the reinforcement phase and the substrate can be improved by plating metal on the outer surface of the reinforcement phase, the operation process is relatively complicated.
经检索,专利公开号为CN101798665A,发明名称为一种铝基泡沫材料的制备方法,首先在碳纤维表明镀覆一层金属,向铝或铝合金熔体中加入带有金属镀层的碳纤维,然后加入氢化钛并搅拌均匀,发泡后取出并冷却得到碳纤维增强的铝基泡沫材料。本发明将碳纤维引入泡沫铝材料的制备之中,实现了气泡的稳定和材料性能的提高。与现有技术相比,本发明制备的泡沫铝材料的压缩强度高于6MPa,冲击韧性提高约30%,能量吸收能力提高50%以上。然而电镀法工艺操作复杂,电镀过程中使用大量的酸、碱、重金属和易燃、易爆及危险化学品等原料,并产生危害人体健康和污染环境的废水、废气、废渣;同样,化学镀法工艺复杂,镀液成分对环境也会造成污染。另外,两种工艺获得的镀层厚度均较薄,不利于增强相与泡沫铝之间形成金属间化合物。After searching, the patent publication number is CN101798665A, and the invention name is a method for preparing an aluminum-based foam material. First, a layer of metal is plated on the surface of the carbon fiber, and the carbon fiber with the metal coating is added to the aluminum or aluminum alloy melt, and then titanium hydride is added and stirred evenly. After foaming, it is taken out and cooled to obtain a carbon fiber-reinforced aluminum-based foam material. The present invention introduces carbon fiber into the preparation of the foam aluminum material, and realizes the stability of the bubbles and the improvement of the material performance. Compared with the prior art, the compression strength of the foam aluminum material prepared by the present invention is higher than 6MPa, the impact toughness is increased by about 30%, and the energy absorption capacity is increased by more than 50%. However, the electroplating process is complicated, and a large amount of acid, alkali, heavy metals and flammable, explosive and dangerous chemicals are used in the electroplating process, and waste water, waste gas and waste residue that are harmful to human health and pollute the environment are generated; similarly, the chemical plating process is complicated, and the composition of the plating solution will also cause pollution to the environment. In addition, the coating thickness obtained by the two processes is relatively thin, which is not conducive to the formation of intermetallic compounds between the reinforcement phase and the foam aluminum.
此外,专利公开号为CN105624451A,发明名称为一种高强高韧泡沫铝及其制备方法。泡沫铝的密度为0.4~1g/cm3,泡孔平均尺寸为2~5mm,其孔壁由铝基体以及均匀弥散在其中的增强颗粒构成,增强颗粒与铝基体形成高强度结合的冶金界面。首先将铝基体粉、增强颗粒和发泡剂颗粒均匀混合并冷压制成粗坯,粗坯经真空热除气之后热变形加工制成可发泡的预制体,经加热发泡制得泡沫铝。按照增强颗粒的体积百分含量为3~25%的比例将铝基体粉末和增强颗粒进行混合。大塑性变形有助于铝基体与增强颗粒实现高强度结合的冶金界面,从而改善发泡过程中增强颗粒与融熔铝基体的润湿性,减少颗粒偏聚,有助于获得颗粒分布均匀的泡沫铝。专利公开号为CN109321787A,发明名称为一种铝基复合材料的制备方法。以可塑性变形的金属颗粒为载体,连同TiH2及增强相进行球磨,使TiH2和增强相镶嵌吸附在载体上,制备得发泡混合体;将铝或铝合金熔体置入坩埚内,在指定温度下,添加适量铝箔包裹的发泡混合体,并进行高速搅拌;取出搅拌设备,对坩埚进行保温沉积;达到指定保温沉积时间后,取出坩埚,并对其冷却,获得泡沫体底部的铝基复合材料。上述方案中首先将金属颗粒、增强相和发泡剂颗粒均匀混合制得发泡混合体,其不足之处在于,获得的增强材料泡孔分布极不均匀,其上部为泡沫层,下部为无泡层的铝基复合材料;并且,增强相连同发泡剂一起与金属颗粒混合,造成增强相包覆不完全,不利于增强相与泡沫金属之间形成金属间化合物。In addition, the patent publication number is CN105624451A, and the invention name is a high-strength and high-toughness foamed aluminum and its preparation method. The density of the foamed aluminum is 0.4-1g/ cm3 , the average size of the pores is 2-5mm, and the pore wall is composed of an aluminum matrix and reinforced particles uniformly dispersed therein, and the reinforced particles and the aluminum matrix form a high-strength metallurgical interface. First, the aluminum matrix powder, the reinforced particles and the foaming agent particles are uniformly mixed and cold-pressed into a rough blank, and the rough blank is heat-degassed by vacuum heat and then heat-deformed to form a foamable preform, and the foamed aluminum is obtained by heating and foaming. The aluminum matrix powder and the reinforced particles are mixed according to a volume percentage of 3-25% of the reinforced particles. Large plastic deformation helps the aluminum matrix and the reinforced particles to achieve a high-strength metallurgical interface, thereby improving the wettability of the reinforced particles and the molten aluminum matrix during the foaming process, reducing particle segregation, and helping to obtain a foamed aluminum with uniform particle distribution. The patent publication number is CN109321787A, and the invention name is a method for preparing an aluminum-based composite material. Plastically deformable metal particles are used as carriers, and ball milling is performed together with TiH2 and a reinforcing phase, so that TiH2 and the reinforcing phase are embedded and adsorbed on the carrier to prepare a foamed mixture; aluminum or aluminum alloy melt is placed in a crucible, and at a specified temperature, an appropriate amount of the foamed mixture wrapped in aluminum foil is added, and high-speed stirring is performed; the stirring device is taken out, and the crucible is subjected to heat preservation deposition; after reaching the specified heat preservation deposition time, the crucible is taken out and cooled to obtain an aluminum-based composite material at the bottom of the foam. In the above scheme, the metal particles, the reinforcing phase and the foaming agent particles are first uniformly mixed to obtain a foamed mixture. The disadvantage is that the obtained reinforcement material has extremely uneven pore distribution, and the upper part is a foam layer and the lower part is an aluminum-based composite material without a foam layer; and the reinforcing phase is mixed with the metal particles together with the foaming agent, resulting in incomplete coating of the reinforcing phase, which is not conducive to the formation of intermetallic compounds between the reinforcing phase and the foamed metal.
发明内容Summary of the invention
1.要解决的问题1. Problem to be solved
针对现有粉末冶金法制备泡沫铝过程中增强相与泡沫铝基体润湿性差的问题,本发明提供一种泡沫铝及其制备方法,利用该方法制得的增强相与泡沫铝基体润湿性好。In view of the problem of poor wettability between a reinforcing phase and a foamed aluminum matrix in the process of preparing foamed aluminum by the existing powder metallurgy method, the present invention provides a foamed aluminum and a preparation method thereof, wherein the reinforcing phase prepared by the method has good wettability with the foamed aluminum matrix.
2.技术方案2. Technical solution
为了解决上述问题,本发明所采用的技术方案如下:In order to solve the above problems, the technical solution adopted by the present invention is as follows:
本发明提供一种泡沫铝的制备方法,具体步骤如下:The present invention provides a method for preparing foamed aluminum, and the specific steps are as follows:
步骤S1、增强相预处理:将增强相与塑性金属粉末按一定质量比混合均匀后压块,破碎、过筛,获得一定粒径且外表面被塑性金属包裹的增强相,记为改性增强相;Step S1, pretreatment of the reinforcement phase: the reinforcement phase and the plastic metal powder are mixed uniformly in a certain mass ratio, and then briquetting is performed, crushing and sieving to obtain a reinforcement phase with a certain particle size and the outer surface of which is coated with the plastic metal, which is recorded as a modified reinforcement phase;
所述增强相为陶瓷颗粒、晶须或短纤维中的一种,所述陶瓷颗粒为SiC或Al2O3颗粒,粒径为200~400目;晶须为莫来石或尖晶石晶须,直径0.2~0.5μm,长径比20~60;短纤维为碳纤维,长度在20~80μm。其中颗粒增强相主要通过陶瓷颗粒的高强度,均匀分散在基体中起到增强作用;晶须与纤维主要利用增强相的高长径比,均匀交织在基体中,起到网状增强效果。所述塑性金属粉末选自铝、铜、镁或锡粉中的一种或多种,其和铝合金形成熔点位于400-550℃的金属间化合物,从而在发泡之前,金属间化合物先熔化对增强相进行润湿,所述塑性金属粉末的粒径范围为500~800目,小于增强相粒径,能最大程度上保证增强相外表面被粒径较小的塑性金属完全包裹。所述增强相与塑性金属粉末的质量比为1:(2~6),增强相过多则包覆率低,导致性能提升率较低;塑性金属粉末过多则增强相添加量相对过低,同样导致性能提升率低。相较于现有技术【马有草.快速粉末冶金发泡法制备碳纳米管增强泡沫铝复合材料及其压缩性能[D].天津大学.】中将碳纳米管直接包覆在泡沫铝基体表面,本发明采用陶瓷相作为增强相,增强效果更显著。The reinforcing phase is one of ceramic particles, whiskers or short fibers. The ceramic particles are SiC or Al2O3 particles with a particle size of 200-400 meshes; the whiskers are mullite or spinel whiskers with a diameter of 0.2-0.5 μm and an aspect ratio of 20-60; the short fibers are carbon fibers with a length of 20-80 μm. The particle reinforcing phase mainly plays a reinforcing role by being evenly dispersed in the matrix due to the high strength of the ceramic particles; the whiskers and fibers mainly utilize the high aspect ratio of the reinforcing phase to be evenly interwoven in the matrix to achieve a mesh reinforcing effect. The plastic metal powder is selected from one or more of aluminum, copper, magnesium or tin powder, and it forms an intermetallic compound with an aluminum alloy with a melting point of 400-550°C, so that before foaming, the intermetallic compound first melts to wet the reinforcing phase. The particle size of the plastic metal powder ranges from 500 to 800 meshes, which is smaller than the particle size of the reinforcing phase, and can ensure to the greatest extent that the outer surface of the reinforcing phase is completely wrapped by the plastic metal with a smaller particle size. The mass ratio of the reinforcing phase to the plastic metal powder is 1:(2-6). If there is too much reinforcing phase, the coating rate is low, resulting in a low performance improvement rate; if there is too much plastic metal powder, the amount of reinforcing phase added is relatively low, which also results in a low performance improvement rate. Compared with the prior art [Ma Youcao. Preparation of carbon nanotube reinforced aluminum foam composite material by rapid powder metallurgy foaming method and its compression performance [D]. Tianjin University.], in which carbon nanotubes are directly coated on the surface of aluminum foam matrix, the present invention uses ceramic phase as reinforcing phase, and the reinforcing effect is more significant.
由于粉末冶金法制备泡沫铝的原料基体为金属粉末,进行发泡之前,要进行压制获得致密度较高的发泡前驱体;由于粉末冶金法制备泡沫铝时外加的增强相与基体只能通过固-固物理结合,结合力较差,导致发泡前驱体致密度不高,因此,本发明在发泡之前将增强相与塑性金属粉末混合,形成表面具有塑性金属包裹的增强相,再与原料基体混合,增强相被塑性较好的金属大范围包裹,在压制过程中将会与金属粉末结合致密,提高了致密度,利于后续发泡。Since the raw material matrix for preparing foamed aluminum by powder metallurgy is metal powder, it is necessary to press before foaming to obtain a foamed precursor with higher density; since the added reinforcing phase and the matrix can only be physically bonded to each other through solid-solid physical bonding when preparing foamed aluminum by powder metallurgy, the bonding force is poor, resulting in low density of the foamed precursor. Therefore, the present invention mixes the reinforcing phase with plastic metal powder before foaming to form a reinforcing phase with plastic metal wrapped on the surface, and then mixes it with the raw material matrix. The reinforcing phase is widely wrapped by the metal with better plasticity, and will be densely combined with the metal powder during the pressing process, thereby improving the density and facilitating subsequent foaming.
所述压块过程在压力为400~600MPa下压块,获得压块厚度为1~2mm,直径为50mm的圆柱体;将压块破碎后过筛,得到粒径范围在100~300目被塑性金属包裹的增强相,记为改性增强相;The briquetting process comprises briquetting under a pressure of 400-600 MPa to obtain a cylindrical briquette with a thickness of 1-2 mm and a diameter of 50 mm; the briquette is crushed and sieved to obtain a reinforcing phase wrapped by plastic metal with a particle size range of 100-300 meshes, which is recorded as a modified reinforcing phase;
步骤S2、制备泡沫铝:取一定质量步骤S1所得改性增强相加入金属粉末原料和发泡剂中混匀,进行泡沫铝的制备,使得增强相与泡沫铝基体润湿性得到改善,从而获得性能增强的泡沫铝材料。粉末冶金法制备泡沫铝的原料包括金属粉末原料、改性增强相和发泡剂,所述改性增强相的加入量为粉末冶金法制备泡沫铝的原料的3.0wt%~9.0wt%,过多则导致发泡过程中基体粘度增大,形成的泡孔结构较差,过少则对泡沫铝的屈服强度提升率有限。改性增强相的包覆率越高,屈服强度越高,当包覆率一定时,改性增强相的添加量越大,屈服强度越高,如图3-4所示,当包覆率一定,为95%时,屈服强度在改性增强相的添加量为3wt%-9wt%的范围内先增大后减小,在添加量为6wt%时,屈服强度提升效果最好。所述金属粉末原料选自200~400目的Al粉、Mg粉或AlMg50合金粉、Si粉或AlSi12合金粉、Cu粉和Sn粉;制备过程中,按Al的质量分数为74~90%、Mg为3~6%、Si为3~8%、Cu为2~6%、Sn为2~6%进行组合形成金属粉末原料;所述发泡剂为氢化钛,发泡剂的加入量为粉末冶金法制备泡沫铝的原料的0.5wt%~1.0wt%,其余组分为金属粉末原料。将改性增强相与金属粉末原料和发泡剂混匀后制备发泡前驱体;发泡前驱体在发泡温度为580~620℃,保温5~20min后冷却获得性能增强的泡沫铝。Step S2, preparing foamed aluminum: taking a certain mass of the modified reinforcing phase obtained in step S1, adding it to the metal powder raw material and the foaming agent, and mixing it, preparing the foamed aluminum, so that the wettability of the reinforcing phase and the foamed aluminum matrix is improved, thereby obtaining a foamed aluminum material with enhanced performance. The raw materials for preparing foamed aluminum by powder metallurgy include metal powder raw materials, modified reinforcing phases and foaming agents. The amount of the modified reinforcing phase added is 3.0wt% to 9.0wt% of the raw materials for preparing foamed aluminum by powder metallurgy. Too much will increase the viscosity of the matrix during the foaming process, and the formed pore structure is poor. Too little will limit the yield strength improvement rate of the foamed aluminum. The higher the coverage rate of the modified reinforcing phase, the higher the yield strength. When the coverage rate is constant, the greater the amount of the modified reinforcing phase added, the higher the yield strength. As shown in Figure 3-4, when the coverage rate is constant, which is 95%, the yield strength increases first and then decreases within the range of 3wt%-9wt% of the modified reinforcing phase added. When the addition amount is 6wt%, the yield strength improvement effect is best. The metal powder raw material is selected from 200-400 mesh Al powder, Mg powder or AlMg50 alloy powder, Si powder or AlSi12 alloy powder, Cu powder and Sn powder; during the preparation process, the metal powder raw material is formed by combining Al with a mass fraction of 74-90%, Mg with a mass fraction of 3-6%, Si with a mass fraction of 3-8%, Cu with a mass fraction of 2-6%, and Sn with a mass fraction of 2-6%; the foaming agent is titanium hydride, and the amount of the foaming agent added is 0.5wt%-1.0wt% of the raw material for preparing foamed aluminum by powder metallurgy, and the remaining components are metal powder raw materials. The modified reinforcing phase is mixed with the metal powder raw material and the foaming agent to prepare a foaming precursor; the foaming precursor is kept at a foaming temperature of 580-620°C for 5-20 minutes and then cooled to obtain foamed aluminum with enhanced performance.
3.有益效果3. Beneficial effects
相比于现有技术,本发明的有益效果为:Compared with the prior art, the present invention has the following beneficial effects:
(1)本发明的一种泡沫铝的制备方法中,采用塑性金属粉末对增强相进行改性,制得的泡沫铝前驱体致密度高,泡沫铝因增强相与基体润湿性能改善使其压缩性能好;(1) In a method for preparing aluminum foam of the present invention, a plastic metal powder is used to modify the reinforcing phase, and the obtained aluminum foam precursor has a high density. The aluminum foam has good compression performance due to the improved wettability between the reinforcing phase and the matrix;
(2)制备过程简单,操作方便,可与粉末冶金法制备泡沫铝工艺实现设备完全共享,不需要任何新增设备,在工业化生产上优势明显。(2) The preparation process is simple and easy to operate. It can fully share equipment with the powder metallurgy process for preparing foamed aluminum, and does not require any additional equipment, which has obvious advantages in industrial production.
附图说明BRIEF DESCRIPTION OF THE DRAWINGS
以下将结合附图和实施例来对本发明的技术方案作进一步的详细描述,但是应当知道,这些附图仅是为解释目的而设计的,因此不作为本发明范围的限定。此外,除非特别指出,这些附图仅意在概念性地说明此处描述的结构构造,而不必要依比例进行绘制。The technical solution of the present invention will be further described in detail below in conjunction with the accompanying drawings and embodiments, but it should be understood that these drawings are designed only for explanation purposes and are not intended to limit the scope of the present invention. In addition, unless otherwise specified, these drawings are intended only to conceptually illustrate the structural configurations described herein and are not necessarily drawn to scale.
图1为实施例3经改性增强相扫描电镜照片;FIG1 is a scanning electron microscope photograph of the modified enhanced phase of Example 3;
图2为实施例3增润湿性改善前后的泡沫铝压缩性能对比;FIG2 is a comparison of the compression properties of aluminum foam before and after the improvement of wettability in Example 3;
图3为改性增强相包覆率对泡沫铝屈服强度提升率的影响,所述改性增强相为莫来石晶须;FIG3 is an effect of the coverage of a modified reinforcing phase on the yield strength improvement rate of aluminum foam, wherein the modified reinforcing phase is mullite whiskers;
图4为改性增强相添加量对泡沫铝屈服强度提升率的影响,所述改性增强相为莫来石晶须。FIG4 shows the effect of the amount of modified reinforcing phase added on the yield strength improvement rate of foamed aluminum, wherein the modified reinforcing phase is mullite whiskers.
具体实施方式DETAILED DESCRIPTION
下文对本发明的示例性实施例的详细描述参考了附图,该附图形成描述的一部分,在该附图中作为示例示出了本发明可实施的示例性实施例。尽管这些示例性实施例被充分详细地描述以使得本领域技术人员能够实施本发明,但应当理解可实现其他实施例且可在不脱离本发明的精神和范围的情况下对本发明作各种改变。下文对本发明的实施例的更详细的描述并不用于限制所要求的本发明的范围,而仅仅为了进行举例说明且不限制对本发明的特点和特征的描述,以提出执行本发明的最佳方式,并足以使得本领域技术人员能够实施本发明。因此,本发明的范围仅由所附权利要求来限定。The following detailed description of exemplary embodiments of the present invention refers to the accompanying drawings, which form a part of the description, and in which exemplary embodiments of the present invention that can be implemented are shown as examples. Although these exemplary embodiments are described in sufficient detail to enable those skilled in the art to implement the present invention, it should be understood that other embodiments can be implemented and various changes can be made to the present invention without departing from the spirit and scope of the present invention. The following more detailed description of the embodiments of the present invention is not intended to limit the scope of the claimed invention, but is only for the purpose of illustrating and not limiting the description of the characteristics and features of the present invention, so as to propose the best mode for performing the present invention and to enable those skilled in the art to implement the present invention. Therefore, the scope of the present invention is limited only by the appended claims.
表1本发明实施例1-5组分参数Table 1 Component parameters of Examples 1-5 of the present invention
表2本发明实施例1-5工艺参数Table 2 Process parameters of Examples 1-5 of the present invention
实施例1Example 1
实施例1提供一种泡沫铝的制备方法,具体步骤如下:Example 1 provides a method for preparing foamed aluminum, and the specific steps are as follows:
步骤S1、增强相预处理:将粒径为400目的SiC颗粒增强相与粒径为800目的铝粉按质量比1:6混合均匀后,在压力为500MPa下压块,获得厚度为1.5mm,直径为50mm的圆柱体,再破碎、过200目筛,获得被金属铝包裹的SiC增强相,其微观形貌类似于图1所示;Step S1, reinforcement phase pretreatment: SiC particle reinforcement phase with a particle size of 400 mesh and aluminum powder with a particle size of 800 mesh are uniformly mixed in a mass ratio of 1:6, and then pressed into blocks at a pressure of 500 MPa to obtain a cylinder with a thickness of 1.5 mm and a diameter of 50 mm, which is then crushed and passed through a 200-mesh sieve to obtain a SiC reinforcement phase wrapped by metal aluminum, whose microstructure is similar to that shown in Figure 1;
步骤S2、制备泡沫铝:取质量分数为7%的经以上预处理的SiC增强相加入粉末冶金法制备泡沫铝的粉末原料中混匀,制备发泡前驱体;发泡前驱体在发泡温度为620℃,保温5min后冷却获得性能增强的泡沫铝。Step S2, preparing foamed aluminum: taking 7% by mass of the SiC reinforcing phase pretreated as above and adding it to the powder raw material for preparing foamed aluminum by powder metallurgy method, mixing, and preparing a foaming precursor; the foaming precursor is kept at a foaming temperature of 620° C. for 5 minutes and then cooled to obtain foamed aluminum with enhanced performance.
制得的改性增强相被塑性金属包裹的包覆率较高,利用该改性增强相制得的泡沫铝压缩性能高,相较于增强相未经改性的泡沫铝,其屈服强度提升率达到95%。The modified reinforcing phase has a high coverage rate of being wrapped by the plastic metal. The foamed aluminum prepared using the modified reinforcing phase has high compression performance. Compared with the foamed aluminum with unmodified reinforcing phase, the yield strength improvement rate reaches 95%.
实施例2Example 2
实施例2提供一种泡沫铝的制备方法,具体步骤如下:Embodiment 2 provides a method for preparing foamed aluminum, and the specific steps are as follows:
步骤S1、增强相预处理:将粒径为200目的Al2O3颗粒增强相与粒径为500目的铝粉按质量比1:3.5混合均匀后,在压力为500MPa下压块,获得厚度为1.5mm,直径为50mm的圆柱体,再破碎、过100目筛,获得被金属铝包裹的Al2O3增强相,其微观形貌类似于图1所示;Step S1, reinforcement phase pretreatment: after uniformly mixing Al 2 O 3 particle reinforcement phase with a particle size of 200 mesh and aluminum powder with a particle size of 500 mesh at a mass ratio of 1:3.5, briquetting was performed at a pressure of 500 MPa to obtain a cylinder with a thickness of 1.5 mm and a diameter of 50 mm, and then crushing and passing through a 100 mesh sieve to obtain an Al 2 O 3 reinforcement phase wrapped by metal aluminum, whose microstructure is similar to that shown in FIG1 ;
步骤S2、制备泡沫铝:取质量分数为9%的经以上预处理的Al2O3增强相加入粉末冶金法制备泡沫铝的粉末原料中混匀,制备发泡前驱体;发泡前驱体在发泡温度为580℃,保温20min后冷却获得性能增强的泡沫铝。Step S2, preparing foamed aluminum: adding 9% of the pretreated Al2O3 reinforcing phase to the powder raw material for preparing foamed aluminum by powder metallurgy and mixing them evenly to prepare a foaming precursor; the foaming precursor is kept at a foaming temperature of 580°C for 20 minutes and then cooled to obtain foamed aluminum with enhanced performance.
实施例3Example 3
实施例3提供一种泡沫铝的制备方法,具体步骤如下:Example 3 provides a method for preparing foamed aluminum, and the specific steps are as follows:
步骤S1、增强相预处理:将直径为0.5μm,长径比为20的莫来石晶须增强相与粒径为600目的锡粉按质量比1:4混合均匀后,在压力为400MPa下压块,获得厚度为1mm,直径为50mm的圆柱体,再破碎、过200目筛,获得被金属铜包裹的莫来石晶须增强相,其微观形貌如图1所示;Step S1, reinforcement phase pretreatment: a mullite whisker reinforcement phase with a diameter of 0.5 μm and an aspect ratio of 20 and a tin powder with a particle size of 600 mesh are uniformly mixed in a mass ratio of 1:4, and then pressed into blocks at a pressure of 400 MPa to obtain a cylinder with a thickness of 1 mm and a diameter of 50 mm, which is then crushed and passed through a 200-mesh sieve to obtain a mullite whisker reinforcement phase wrapped by metal copper, the microstructure of which is shown in FIG1 ;
步骤S2、制备泡沫铝:取质量分数为7.5%的经以上预处理的莫来石晶须增强相加入粉末冶金法制备泡沫铝的粉末原料中混匀,制备发泡前驱体;发泡前驱体在发泡温度为600℃,保温15min后冷却获得性能增强的泡沫铝,润湿性能改善前后获得的泡沫铝力学性能对比如图2所示。Step S2, preparing foamed aluminum: taking 7.5% by mass of the mullite whisker reinforcement phase pretreated as above, adding it to the powder raw material for preparing foamed aluminum by powder metallurgy method and mixing it evenly to prepare a foaming precursor; the foaming precursor is foamed at a temperature of 600°C, kept warm for 15 minutes and then cooled to obtain foamed aluminum with enhanced performance. The mechanical properties of the foamed aluminum obtained before and after the improvement of the wettability are compared as shown in Figure 2.
实施例4Example 4
实施例4提供一种泡沫铝的制备方法,具体步骤如下:Example 4 provides a method for preparing foamed aluminum, and the specific steps are as follows:
步骤S1、增强相预处理:将直径为0.2μm,长径比为60的尖晶石晶须增强相与粒径为500目的镁粉按质量比1:4混合均匀后,在压力为400MPa下压块,获得厚度为2mm,直径为50mm的圆柱体,再破碎、过200目筛,获得被金属镁包裹的尖晶石晶须增强相,其微观形貌类似于图1所示;Step S1, reinforcement phase pretreatment: a spinel whisker reinforcement phase with a diameter of 0.2 μm and an aspect ratio of 60 and a magnesium powder with a particle size of 500 mesh are uniformly mixed in a mass ratio of 1:4, and then pressed into blocks at a pressure of 400 MPa to obtain a cylinder with a thickness of 2 mm and a diameter of 50 mm, which is then crushed and passed through a 200-mesh sieve to obtain a spinel whisker reinforcement phase wrapped by metal magnesium, whose microstructure is similar to that shown in FIG1 ;
步骤S2、制备泡沫铝:取质量分数为5%的经以上预处理的尖晶石晶须增强相加入粉末冶金法制备泡沫铝的粉末原料中混匀,制备发泡前驱体;发泡前驱体在发泡温度为610℃,保温10min后冷却获得性能增强的泡沫铝。Step S2, preparing foamed aluminum: taking 5% by mass of the spinel whisker reinforcement phase pretreated as above and adding it to the powder raw material for preparing foamed aluminum by powder metallurgy method, mixing, and preparing a foaming precursor; the foaming precursor is kept at a foaming temperature of 610° C. for 10 minutes and then cooled to obtain foamed aluminum with enhanced performance.
实施例5Example 5
实施例5提供一种泡沫铝的制备方法,具体步骤如下:Example 5 provides a method for preparing foamed aluminum, and the specific steps are as follows:
步骤S1、增强相预处理:将长度为40μm碳纤维增强相与粒径为500目的铜粉按质量比1:2混合均匀后,在压力为600MPa下压块,获得厚度为1mm,直径为50mm的圆柱体,再破碎、过300目筛,获得被金属锡包裹的碳纤维增强相,其微观形貌类似于图1所示;Step S1, reinforcement phase pretreatment: a carbon fiber reinforcement phase with a length of 40 μm and a copper powder with a particle size of 500 mesh are uniformly mixed in a mass ratio of 1:2, and then pressed into blocks at a pressure of 600 MPa to obtain a cylinder with a thickness of 1 mm and a diameter of 50 mm, which is then crushed and passed through a 300-mesh sieve to obtain a carbon fiber reinforcement phase wrapped by metal tin, whose microstructure is similar to that shown in FIG1 ;
步骤S2、制备泡沫铝:取质量分数为3%的经以上预处理的碳纤维增强相加入粉末冶金法制备泡沫铝的粉末原料中混匀,制备发泡前驱体;发泡前驱体在发泡温度为590℃,保温15min后冷却获得性能增强的泡沫铝。Step S2, preparing foamed aluminum: taking 3% by mass of the carbon fiber reinforcement phase pretreated as above and adding it to the powder raw material for preparing foamed aluminum by powder metallurgy method, mixing them evenly, to prepare a foaming precursor; the foaming precursor is kept at a foaming temperature of 590° C. for 15 minutes and then cooled to obtain foamed aluminum with enhanced performance.
以上所述仅为本发明的优选实施方案,应当指出,对于本技术领域的普通技术人员来说,在不脱离本发明技术原理的前提下,还可以做出若干改进和润饰,这些改进和润饰也应视为本发明的保护范围。The above is only a preferred embodiment of the present invention. It should be pointed out that for ordinary technicians in this technical field, several improvements and modifications can be made without departing from the technical principles of the present invention. These improvements and modifications should also be regarded as the scope of protection of the present invention.
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| CN109317690A (en) * | 2018-09-28 | 2019-02-12 | 天津大学 | A kind of preparation method of graphene reinforced aluminum-based composite foam material |
| CN111979440A (en) * | 2020-08-20 | 2020-11-24 | 安徽工业大学 | Aluminum alloy component for preparing foamed aluminum by powder metallurgy method and foaming method |
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| DE102011118295A1 (en) * | 2011-11-10 | 2013-05-16 | Daimler Ag | Producing an aluminum foam body, comprises providing a microporous body made of aluminum alloy reinforced with hard material particles, and melting the microporous body and then treating a melt under vacuum by acting upon with vibrations |
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| CN111979440A (en) * | 2020-08-20 | 2020-11-24 | 安徽工业大学 | Aluminum alloy component for preparing foamed aluminum by powder metallurgy method and foaming method |
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