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JP3485720B2 - Manufacturing method of metal matrix composite material - Google Patents
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JP3485720B2 - Manufacturing method of metal matrix composite material - Google Patents

Manufacturing method of metal matrix composite material

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Publication number
JP3485720B2
JP3485720B2 JP11214796A JP11214796A JP3485720B2 JP 3485720 B2 JP3485720 B2 JP 3485720B2 JP 11214796 A JP11214796 A JP 11214796A JP 11214796 A JP11214796 A JP 11214796A JP 3485720 B2 JP3485720 B2 JP 3485720B2
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JP
Japan
Prior art keywords
particles
metal
composite material
stirring
molten metal
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.)
Expired - Lifetime
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JP11214796A
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Japanese (ja)
Other versions
JPH09279268A (en
Inventor
喜和 弦間
好樹 恒川
尚武 毛利
正洋 奥宮
優子 棚田
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Toyota Motor Corp
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Toyota Motor Corp
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Description

【発明の詳細な説明】 【0001】 【発明の属する技術分野】本発明は、金属または合金か
ら成る第一相マトリックス中に第二相粒子を分散させた
金属基複合材料を、渦流攪拌を用いた鋳造法により製造
する方法に関する。 【0002】 【従来の技術】金属基複合材料(MMC:Metal Matrix
Composite)の典型例としては、金属または合金から成
るマトリックス(第一相もしくは基材)中に第二相とし
てセラミック等の強化粒子を分散させたものが知られて
いる。強化粒子等の第二相粒子の形状としては、粒状、
ウィスカー、繊維等が用いられる。特に、アルミニウム
基、マグネシウム基の金属基複合材料は、軽量性、比強
度、比剛性等の点で優れている。 【0003】金属基複合材料の代表的な製造方法として
は、溶射法、鋳造法、焼結法、メッキ法等がある。その
うちでも特に鋳造法は、高い生産性が得られるため、既
に多くの実用化例が知られている(例えば、雑誌「金
属」1992年、5月号、48〜55頁を参照)。鋳造
法においては、鋳造すべき金属または合金の溶湯(以下
「金属溶湯」と略称)中に強化粒子等の第二相粒子を分
散させる液相プロセスが、マトリックス中に第二相粒子
を均一分散させる上で特に重要である。液相プロセスの
代表的なものとして、溶浸法および渦流攪拌法がある
が、特に第二相粒子としてセラミック粒子等の、金属溶
湯に対する濡れ性が低い粒子を用いる場合には、いずれ
の場合にも特別な設備や処理あるいは合金組成の調整が
必要となる。 【0004】すなわち、溶浸法では、低い濡れ性を補う
のに必要な高圧を負荷するための大規模な設備が必要に
なる。また、渦流攪拌法では、粒子を分散させるために
長時間の攪拌が必要なばかりでなく、たとえ攪拌を長時
間行っても微粒子を均一に分散せることは極めて困難で
ある。例えばセラミック粒子のアルミニウム溶湯に対す
る濡れ性を表す一つのパラメータとして、セラミック粒
子に働く重力(体積に起因する沈降力)と表面張力(表
面積に起因する浮上力)とのバランスがあるが、粒子が
小さくなるほど、体積に対して表面積の影響が大きくな
り、金属溶湯中に微粒子を移行させることが困難にな
る。 【0005】このように、第二相粒子をマトリックス中
に均一分散させる上で、両者間の濡れ性が低いことが大
きな障害となる。そのため従来は、濡れ性を改善する目
的で、粒子表面にコーティング処理を行ったり、金属溶
湯の温度を高くしたり、あるいは金属溶湯中に濡れ性向
上のための合金元素としてMg、Li、Ca、Sr、T
i、Cu等を添加したりする方法が採られていた。 【0006】 【発明が解決しようとする課題】本発明は、第二相粒子
がセラミック粒子のような金属溶湯との濡れ性が低い粒
子であっても、またサブミクロン級の微粒子であって
も、マトリックス中に均一に分散させることができる、
渦流攪拌を用いた鋳造法により金属基複合材料の製造方
法を提供することを目的とする。 【0007】 【課題を解決するための手段】上記の目的は、本発明に
よれば、Al−5mass%Mg合金から成る第一相マトリ
クス中にAlから成る第二相粒子を分散させた金
属基複合材料を、渦流攪拌を用いた鋳造法により製造す
る方法において、上記Al−5mass%Mg合金の溶湯に
上記第二相粒子を添加し、該溶湯に超音波振動を印加し
ながら上記渦流攪拌を行なうことを特徴とする金属基複
合材料の製造方法によって達成される。本発明において
超音波振動としては、一般に20kHz以上の周波数の
振動を用いる。 【0008】 【発明の実施の形態】図1に、鋳造法により金属基複合
材料を製造する際に、本発明の方法により金属溶湯に第
二相粒子を分散混合するための超音波渦流攪拌装置の構
成例を示す。この装置は、超音波振動子1と超音波ホー
ン2と超音波振動板3がこの順に接続されて構成された
超音波振動系を備えている。超音波振動子1で発生した
超音波振動は、ホーン2を介して超音波振動板3から坩
堝14内の金属溶湯13に伝達される。超音波振動子1
には、超音波信号発生器および高周波増幅器から成る発
振部4と、共振周波数追尾回路5とが接続されている。
追尾回路5により共振周波数を所定周波数(例えば20
kHz)に維持する。 【0009】所定の金属または合金を坩堝14内に装入
し、加熱手段15により加熱して溶湯13を形成する。
溶湯13を渦流攪拌するために、モータドライバー6に
よりモータ7を制御駆動し、モータ7の軸の先端に取り
付けた回転子8を300〜1000rpm程度で定速回
転させる。 【0010】ホッパー12に貯留されている強化粒子等
の第二相粒子9は、ボンベ10からのキャリアガス(例
えば窒素)により予熱炉11を経た後に溶湯13上に供
給される。 【0011】 【実施例】図1に示した装置を用い、本発明により、A
lまたはAl−5mass%Mg合金をマトリックスとしA
2 3 を強化粒子とする金属基複合材料を製造した。
Al2 3 粒子の直径は、50μm、3μm、0.1μ
mとした。比較のために、図1に示した超音波振動系を
作動させずに従来の渦流攪拌のみを用いた方法の行っ
た。 【0012】本発明法および比較法について、用いたプ
ロセス条件、金属溶湯、Al2 3強化粒子の直径をま
とめて示す。 【0013】 【表1】【0014】先ず顆粒状あるいは断片状等のAlまたは
Al−5mass%Mg合金を坩堝14内に装入し、窒素ガ
ス雰囲気中にて加熱装置15により1023Kまで加熱
し溶解した。坩堝13内に形成された溶湯13中で攪拌
子8を300rpmで定速回転させて渦流攪拌しなが
ら、超音波振動系により共振周波数20kHzで振動板
3を超音波振動させた。ただし比較法では超音波振動は
行わなかった。種々の攪拌時間後に鋳造して、本発明に
よる実施例サンプル1〜4と従来法による比較例サンプ
ル5〜8を得た。 【0015】図2に、得られた各サンプルについて、攪
拌時間とAl2 3 粒子体積率との関係を示す。いずれ
も、塗り潰したプロットは本発明による実施例サンプル
のデータであり、白抜きのプロットは従来法による比較
例のサンプルのデータである。ここでAl2 3 粒子体
積率は、図3に示したビッカース硬さとの関係を予め求
めておき、各サンプルについてビッカース硬さの測定値
から粒子体積率に換算した。 【0016】まず、Al溶湯中に直径50μmのAl2
3 粒子を添加した場合について、本発明のサンプル1
と比較例のサンプル5とを比較する。従来通り超音波振
動を印加せずに渦流攪拌のみを行った比較例サンプル5
(図2中の△プロット(以下同様))では、1800秒
の攪拌を行ってもAl2 3粒子体積率は0 vol%であ
り、Alマトリックス中へのAl2 3 粒子の分散はな
されておらず、複合化されていない。 【0017】これに対して、本発明により超音波振動を
印加しながら渦流攪拌を行った実施例サンプル1(▲)
では、攪拌時間900秒で既に2.5 vol%程度の体積
率が得られており、攪拌時間が長くなるとともに体積率
は増加し、攪拌時間1800秒では5 vol%程度の体積
率が得られている。次に、Al−5mass%Mg合金溶湯
中に直径50μm、3μm、または0.1μmのAl2
3 粒子を添加した場合について、本発明のサンプル2
〜4と比較例のサンプル6〜8とを比較する。 【0018】粒子径50μmの場合は、従来通り渦流攪
拌のみを行った比較例サンプル6(○)でも、攪拌時間
300秒から1800秒についてAl2 3 粒子体積率
として5 vol%程度から7.5 vol%程度が得られてい
る。これに対して、本発明により超音波振動を印加しな
がら渦流攪拌を行った実施例サンプル2(●)では、同
じ範囲の攪拌時間について9 vol%から10 vol%の体
積率が得られており、Al2 3 粒子体積率が著しく向
上していることが分かる。 【0019】粒子径3μmおよび0.1μmの場合は、
渦流攪拌のみを行った比較例サンプル7(□)および8
(◇)では1800秒までの渦流攪拌で全く複合化され
なかった。これに対して、本発明により超音波振動を印
加しながら渦流攪拌を行った実施例サンプル3(■)お
よび4(◆)では、攪拌時間1800秒でそれぞれ7vo
l%および2.5 vol%程度のAl2 3 粒子体積率が
得られており、従来は複合化できなかった小さい直径の
粒子についても複合化されていることが分かる。 【0020】また、各サンプルの断面の顕微鏡観察を行
い、Al2 3 粒子の複合化状態を調べた。Al−5ma
ss%Mgマトリックス、Al2 3 粒子直径50μm、
攪拌時間900秒の場合の断面組織を、比較例サンプル
6および実施例サンプル2について、図4(a)および
(b)にそれぞれ示す。図4(a)に示したように、従
来通り渦流攪拌のみを行った比較例サンプル6では、A
2 3 粒子が金属溶湯に完全に濡れていなかったた
め、空洞としての欠陥部分(球形でない黒色部分)が多
数認められた。 【0021】これに対して、図4(b)に示したよう
に、本発明により超音波振動を印加しながら渦流攪拌を
行った実施例サンプル2では、Al2 3 粒子が金属溶
湯に完全に濡れたことにより、欠陥は全く認められず、
Al−5mass%Mgマトリックス中にAl2 3 粒子が
均一に分散している。 【0022】 【発明の効果】以上説明したように、金属溶湯に超音波
振動を印加しながら渦流攪拌する本発明の方法によれ
ば、単に渦流攪拌のみを用いた従来の方法に比べて短時
間の攪拌により高い体積率で第二相粒子を均一に分散さ
せた金属基複合材料を製造することができる。更に、本
発明によれば、従来では複合化が極めて困難であった数
μm以下の微粒子でも容易に複合化することができる。
また、超音波振動の印加により第二相粒子の表面が完全
に濡れ、欠陥が発生しない。
Description: BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a metal-based composite material in which a second-phase particle is dispersed in a first-phase matrix made of a metal or an alloy. The present invention relates to a method of manufacturing by a casting method. [0002] Metal Matrix Composite (MMC)
As a typical example of Composite, there is known a matrix in which reinforcing particles such as ceramics are dispersed as a second phase in a matrix (first phase or base material) made of a metal or an alloy. As the shape of the second phase particles such as reinforcing particles, granular,
Whiskers, fibers and the like are used. In particular, aluminum-based and magnesium-based metal-based composite materials are excellent in light weight, specific strength, specific rigidity, and the like. [0003] Typical production methods for metal matrix composite materials include thermal spraying, casting, sintering, and plating. Among them, particularly, the casting method has already been known for many practical applications since high productivity can be obtained (for example, see the magazine “Metal”, May, 1992, pages 48 to 55). In the casting method, a liquid phase process in which second phase particles such as reinforcing particles are dispersed in a molten metal or alloy to be cast (hereinafter abbreviated as “metal molten metal”) involves uniformly dispersing the second phase particles in a matrix. It is particularly important in making Typical examples of the liquid phase process include an infiltration method and a vortex stirring method.In particular, when particles having low wettability to a molten metal, such as ceramic particles, are used as the second phase particles, in any case, However, special equipment, treatment or adjustment of the alloy composition is required. That is, the infiltration method requires a large-scale facility for applying a high pressure necessary to compensate for low wettability. In addition, in the vortex stirring method, not only long time stirring is required to disperse the particles, but even if stirring is performed for a long time, it is extremely difficult to uniformly disperse the fine particles. For example, as one parameter indicating the wettability of ceramic particles to molten aluminum, there is a balance between gravity (settling force due to volume) acting on ceramic particles and surface tension (lifting force due to surface area). Indeed, the effect of the surface area on the volume increases, making it difficult to transfer fine particles into the molten metal. [0005] As described above, in uniformly dispersing the second phase particles in the matrix, low wettability between the two is a major obstacle. Therefore, conventionally, for the purpose of improving the wettability, a coating treatment is performed on the particle surface, or the temperature of the molten metal is increased, or Mg, Li, Ca, as an alloy element for improving the wettability in the molten metal, Sr, T
The method of adding i, Cu, etc. has been adopted. SUMMARY OF THE INVENTION The present invention relates to a method for producing a second phase particle, which is a particle having a low wettability with a molten metal such as a ceramic particle, or a submicron class particle. Can be evenly dispersed in the matrix,
An object of the present invention is to provide a method for producing a metal matrix composite material by a casting method using vortex stirring. SUMMARY OF THE INVENTION According to the present invention, there is provided, in accordance with the present invention, a method of dispersing second phase particles of Al 2 O 3 in a first phase matrix of an Al- 5 mass % Mg alloy. In the method for producing the metal-based composite material by a casting method using vortex stirring, the above-mentioned second phase particles are added to the above-mentioned molten metal of Al-5 mass % Mg alloy, This is achieved by a method for producing a metal-based composite material, which comprises performing vortex stirring. In the present invention, vibration having a frequency of 20 kHz or more is generally used as the ultrasonic vibration. FIG. 1 shows an ultrasonic vortex stirrer for dispersing and mixing second phase particles in a molten metal by a method of the present invention when a metal matrix composite material is manufactured by a casting method. An example of the configuration will be described. This apparatus includes an ultrasonic vibration system in which an ultrasonic vibrator 1, an ultrasonic horn 2, and an ultrasonic vibration plate 3 are connected in this order. Ultrasonic vibration generated by the ultrasonic vibrator 1 is transmitted from the ultrasonic vibration plate 3 to the molten metal 13 in the crucible 14 via the horn 2. Ultrasonic transducer 1
Is connected to an oscillation section 4 composed of an ultrasonic signal generator and a high-frequency amplifier, and a resonance frequency tracking circuit 5.
The tracking circuit 5 sets the resonance frequency to a predetermined frequency (for example, 20
(kHz). [0009] A predetermined metal or alloy is charged into a crucible 14 and heated by a heating means 15 to form a molten metal 13.
In order to vortex the molten metal 13, the motor 7 is controlled and driven by the motor driver 6, and the rotor 8 attached to the tip of the shaft of the motor 7 is rotated at a constant speed of about 300 to 1000 rpm. The second phase particles 9 such as reinforced particles stored in the hopper 12 are supplied onto the molten metal 13 after passing through a preheating furnace 11 by a carrier gas (for example, nitrogen) from a cylinder 10. DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS The apparatus shown in FIG.
l or Al-5mass% Mg alloy as matrix
to produce a metal matrix composite material to strengthen particles l 2 O 3.
The diameter of the Al 2 O 3 particles is 50 μm, 3 μm, 0.1 μm.
m. For comparison, a conventional method using only vortex agitation without operating the ultrasonic vibration system shown in FIG. 1 was performed. For the method of the present invention and the comparative method, the process conditions used, the molten metal, and the diameter of the Al 2 O 3 reinforcing particles are shown together. [Table 1] First, Al or Al-5 mass% Mg alloy in the form of granules or fragments was charged into the crucible 14 and heated and melted to 1023 K in a nitrogen gas atmosphere by the heating device 15. The vibrating plate 3 was ultrasonically vibrated at a resonance frequency of 20 kHz by an ultrasonic vibration system while vortexing and stirring the stirrer 8 at a constant speed of 300 rpm in the molten metal 13 formed in the crucible 13. However, no ultrasonic vibration was performed in the comparative method. Casting was performed after various stirring times to obtain Examples 1 to 4 according to the present invention and Comparative Examples 5 to 8 according to the conventional method. FIG. 2 shows the relationship between the stirring time and the volume fraction of Al 2 O 3 particles for each of the obtained samples. In each case, the filled plot is the data of the sample of the example according to the present invention, and the white plot is the data of the sample of the comparative example according to the conventional method. Here, the relationship between the Al 2 O 3 particle volume ratio and the Vickers hardness shown in FIG. 3 was obtained in advance, and the particle volume ratio was converted from the measured value of the Vickers hardness for each sample. First, Al 2 having a diameter of 50 μm was placed in an Al melt.
Sample 1 of the present invention when O 3 particles were added
And Sample 5 of Comparative Example are compared. Comparative example sample 5 in which only vortex agitation was performed without applying ultrasonic vibration as before.
In the plot (△ plot in FIG. 2 (the same applies hereinafter)), the volume ratio of Al 2 O 3 particles is 0 vol% even after stirring for 1800 seconds, and the Al 2 O 3 particles are dispersed in the Al matrix. Not complexed. On the other hand, according to the present invention, sample 1 of the embodiment in which vortex agitation is performed while applying ultrasonic vibration (▲).
In the above, a volume ratio of about 2.5 vol% has already been obtained with a stirring time of 900 seconds, and the volume ratio increases with increasing stirring time, and a volume ratio of about 5 vol% is obtained with a stirring time of 1800 seconds. ing. Next, a 50 μm, 3 μm, or 0.1 μm diameter Al 2 was added into the Al-5 mass% Mg alloy melt.
In the case where O 3 particles were added, Sample 2 of the present invention was used.
4 and Comparative Examples 6 to 8 are compared. In the case of a particle diameter of 50 μm, even in the comparative sample 6 ()) in which only vortexing was performed as in the past, the volume ratio of Al 2 O 3 particles was about 5 vol% to 7.000 for a stirring time of 300 seconds to 1800 seconds. About 5 vol% is obtained. In contrast, in Example 2 (●) in which vortex stirring was performed while applying ultrasonic vibration according to the present invention, a volume ratio of 9 vol% to 10 vol% was obtained for the same range of stirring time. It can be seen that the volume ratio of Al 2 O 3 particles is remarkably improved. When the particle diameters are 3 μm and 0.1 μm,
Comparative samples 7 (□) and 8 in which only vortex stirring was performed
In (◇), no compound was formed by vortex stirring up to 1800 seconds. On the other hand, in the sample samples 3 (お よ び) and 4 (◆) in which vortex stirring was performed while applying ultrasonic vibration according to the present invention, each of the samples was 7 vowels with a stirring time of 1800 seconds.
Al 2 O 3 particle volume ratios of about 1% and 2.5 vol% were obtained, and it can be seen that particles having a small diameter, which could not be compounded conventionally, were also compounded. The cross section of each sample was observed under a microscope to examine the composite state of the Al 2 O 3 particles. Al-5ma
ss% Mg matrix, Al 2 O 3 particle diameter 50 μm,
FIGS. 4A and 4B show the cross-sectional structures when the stirring time is 900 seconds for Comparative Sample 6 and Example Sample 2, respectively. As shown in FIG. 4A, in Comparative Sample 6 in which only vortex stirring was performed as in the conventional case, A
Since the l 2 O 3 particles were not completely wetted by the molten metal, a large number of defective portions (black portions that were not spherical) were recognized as cavities. On the other hand, as shown in FIG. 4B, in the sample 2 of the present invention in which the vortex agitation is performed while applying the ultrasonic vibration according to the present invention, the Al 2 O 3 particles are completely in the molten metal. Defects are not recognized at all by getting wet,
Al 2 O 3 particles are uniformly dispersed in an Al- 5 mass% Mg matrix. As described above, according to the method of the present invention in which vortex stirring is performed while applying ultrasonic vibration to a molten metal, a shorter time is required as compared with the conventional method using only vortex stirring. By the stirring, a metal matrix composite material in which the second phase particles are uniformly dispersed at a high volume ratio can be manufactured. Further, according to the present invention, even fine particles having a size of several μm or less, which were conventionally extremely difficult to be composited, can be easily composited.
Further, the surface of the second phase particles is completely wetted by the application of the ultrasonic vibration, and no defect occurs.

【図面の簡単な説明】 【図1】図1は、本発明による金属基複合材料の製造方
法を行うための超音波渦流攪拌装置の構成例を示す配置
図である。 【図2】図2は、図1の装置を用いて製造したAl基ま
たはAl−5mass%Mg合金基の金属基複合材料中のA
2 3 粒子体積率と攪拌時間との関係を、従来法によ
る比較例と比較して示すグラフである。 【図3】図3は、Al2 3 粒子体積率と硬さとの関係
を示すグラフである。 【図4】図4は、本発明および従来法により製造したA
l−5mass%Mg合金基複合材料の金属組織を示す顕微
鏡写真である。 【符号の説明】 1…超音波振動子 2…超音波ホーン 3…超音波振動板 4…発振部 5…共振周波数追尾回路 6…モータドライバー 7…モータ 8…回転子 9…第二相粒子 10…ボンベ 11…予熱炉 12…ホッパー 13…金属溶湯 14…坩堝 15…加熱手段
BRIEF DESCRIPTION OF THE DRAWINGS FIG. 1 is a layout diagram showing a configuration example of an ultrasonic vortex stirrer for performing a method for producing a metal matrix composite material according to the present invention. FIG. 2 is a diagram showing A in an Al-based or Al-5 mass% Mg alloy-based metal-based composite material manufactured using the apparatus of FIG. 1;
the relationship between l 2 O 3 particle volume ratio and stirring time is a graph showing comparison with a comparative example according to the conventional method. FIG. 3 is a graph showing the relationship between Al 2 O 3 particle volume ratio and hardness. FIG. 4 shows A and A produced by the present invention and the conventional method.
It is a microscope picture which shows the metal structure of a 1-5 mass% Mg alloy base composite material. [Description of Signs] 1 ... Ultrasonic vibrator 2 ... Ultrasonic horn 3 ... Ultrasonic vibrating plate 4 ... Oscillator 5 ... Resonance frequency tracking circuit 6 ... Motor driver 7 ... Motor 8 ... Rotator 9 ... Second phase particle 10 ... cylinder 11 ... preheating furnace 12 ... hopper 13 ... molten metal 14 ... crucible 15 ... heating means

───────────────────────────────────────────────────── フロントページの続き (72)発明者 弦間 喜和 愛知県豊田市トヨタ町1番地 トヨタ自 動車株式会社内 (72)発明者 恒川 好樹 愛知県岡崎市竜美南2−5−8 (72)発明者 毛利 尚武 愛知県名古屋市天白区八事石坂661−51 (72)発明者 奥宮 正洋 愛知県名古屋市天白区天白町大字島田字 黒石3785番地の3391 (72)発明者 棚田 優子 愛知県名古屋市天白区久方2−12 豊田 工業大学内 (56)参考文献 特開 平2−197536(JP,A) 特開 平5−65564(JP,A) 特公 平3−46533(JP,B2) 特公 平6−13721(JP,B2) (58)調査した分野(Int.Cl.7,DB名) C22C 1/10 B22D 19/00 B22D 19/14 ────────────────────────────────────────────────── ─── Continuing on the front page (72) Inventor Yoshika Tsuruma 1 Toyota Town, Toyota City, Aichi Prefecture Inside Toyota Motor Corporation (72) Inventor Yoshiki Tsunekawa 2-5-8 Ryumi Minami, Okazaki City, Aichi Prefecture (72 Inventor Naotake Mohri 661-51 Yagoto Ishizaka, Tempaku-ku, Nagoya City, Aichi Prefecture (72) Inventor Masahiro Okumiya 3785, Kuroishi, Shimada, Tenjiro-cho, Tenpaku-ku, Nagoya City, Aichi Prefecture 3391 (72) Inventor Yuko Tanada, Nagoya City, Aichi Prefecture 2-12 Hisakata, Tenpaku-ku Toyota Technological Institute (56) References JP-A-2-197536 (JP, A) JP-A-5-65564 (JP, A) JP 3-46533 (JP, B2) Kohei 6-13721 (JP, B2) (58) Fields investigated (Int. Cl. 7 , DB name) C22C 1/10 B22D 19/00 B22D 19/14

Claims (1)

(57)【特許請求の範囲】 【請求項1】 Al−5mass%Mg合金から成る第一相
マトリクス中にAlから成る第二相粒子を分散さ
せた金属基複合材料を、渦流攪拌を用いた鋳造法により
製造する方法において、 上記Al−5mass%Mg合金の溶湯に上記第二相粒子を
添加し、該溶湯に超音波振動を印加しながら上記渦流攪
拌を行なうことを特徴とする金属基複合材料の製造方
法。
(57) [Claim 1] Vortex stirring of a metal matrix composite material in which second phase particles made of Al 2 O 3 are dispersed in a first phase matrix made of an Al- 5 mass % Mg alloy. Wherein the second phase particles are added to a molten metal of the Al-5 mass % Mg alloy, and the vortex stirring is performed while applying ultrasonic vibration to the molten metal. A method for producing a metal matrix composite material.
JP11214796A 1996-04-10 1996-04-10 Manufacturing method of metal matrix composite material Expired - Lifetime JP3485720B2 (en)

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CN102108450B (en) * 2009-12-25 2012-08-29 清华大学 Method for preparing magnesium-based composite material
CN102108455B (en) * 2009-12-25 2013-11-06 清华大学 Preparation method of aluminum-base composite material
CN101851716B (en) * 2010-06-14 2014-07-09 清华大学 Magnesium base composite material and preparation method thereof, and application thereof in sounding device

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