JPH0122331B2 - - Google Patents
Info
- Publication number
- JPH0122331B2 JPH0122331B2 JP56190833A JP19083381A JPH0122331B2 JP H0122331 B2 JPH0122331 B2 JP H0122331B2 JP 56190833 A JP56190833 A JP 56190833A JP 19083381 A JP19083381 A JP 19083381A JP H0122331 B2 JPH0122331 B2 JP H0122331B2
- Authority
- JP
- Japan
- Prior art keywords
- fibers
- fiber
- metal
- inorganic
- nickel
- 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
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Landscapes
- Manufacture Of Alloys Or Alloy Compounds (AREA)
Description
本発明は無機繊維強化金属複合材料に関するも
のである。
近時軽量で、耐熱性にすぐれ、かつ圧縮強度、
引張強度などの機械強度が大きい材料がタービン
ブレード航空機部材などの材料として要望される
ようになつた。
この種の材料としてチタン又はニツケルなどの
金属を炭素繊維、ボロン繊維、アルミナ繊維又は
シリコンカーバイド繊維などの無機繊維で強化し
た無機繊維強化複合材料が提案されている。
従来、この無機繊維強化複合材料はチタン、ニ
ツケルなどの金属粉を無機繊維とともに成形型内
に配列して加熱することにより得られていた。し
かしこの方法で得た無機繊維強化金属複合材料は
例えば無機繊維にシリコンカーバイドを用い、金
属にニツケルを用いた場合には焼結工程において
のニツケルがニツケルカーバイド及びニツケルけ
い素に転化するので、得られる製品の強度が低下
し脆くなる欠点を有している。また、無機繊維に
炭素繊維を、金属にチタンを用いた場合には、得
られる製品はチタンが炭化されるので、上述の複
合材料と同じように強度が弱く脆い欠点がある。
また、ボロン繊維、アルミナ繊維の複合も繊維
と金属界面でやはり反応が起こり十分な複合がな
されない。
本発明者らはこのような欠点を排除した無機繊
維強化金属複合材料を製造する方法を提供するよ
う研究した結果、ボロン繊維、アルミナ繊維、又
はシリコンカーバイド繊維から選ばれた無機繊維
とチタン、ニツケル及びこれらを主体とする合金
との間に限定された厚みのアルミニウム層を介在
させて複合させれば、複合すべき金属は無機繊維
と反応する時間が激減されて複合金属の炭化物又
はけい素化物等が生成せず得られる無機繊維金属
複合材は高度に強化されるとの知見を得て、本発
明を完成するにいたつた。
本発明の要旨はボロン繊維、アルミナ繊維、又
はシリコンカーバイド繊維から選ばれた無機繊維
の表面に0.5〜10μ厚みのアルミニウムの皮膜を形
成し、その無機繊維と粉末又は箔状のチタン、ニ
ツケル及びこれらを主体とする合金とを成形型内
に配列し、ついで加圧下で加熱成形して無機繊維
強化金属複合材料を製造するものである。繊維の
径が5〜140μ程度のアルミナ繊維、シリコンカ
ーバイド繊維が好適に使用される。
複合する金属にはチタン、ニツケル、及びこれ
らを主体とした合金が有効である。
アルミニウムを無機繊維に皮膜を形成するには
イオンプレーテイング法(蒸着法)、含浸法又は
浸漬法によつて得られる。
含浸法はアルミニウムの溶湯の中に無機繊維を
浸し、加圧する方法でありこの場合溶湯の温度は
700〜750℃、圧力は50〜100Kg/cm2が目安となる。
溶湯中減圧下で無機繊維表面に低溶融点金属の薄
膜が形成する場合には溶湯の温度は700〜750℃で
1torr以下で行なう。
アルミニウム皮膜の厚みは0.5〜10μであること
が好ましい。この範囲の皮膜を形成させる程度で
はアルミニウムと繊維とはカーバイドを形成しな
い。厚みは溶湯の温度又は蒸着法の場合には蒸着
量によつて調整される。厚みが0.5μ以下であると
金属と無機繊維とが反応し合うので好ましくな
く、厚みが10μ以上であると低溶融点金属が多く
なり、複合する金属の接着効果が薄れるので好ま
しくない。
複合する金属は箔状(厚み50〜100μ)あるい
は粉末状(粒径40μ以下)のものを使用し、その
成形条件は加熱温度は800〜1000℃、圧力は100〜
1000Kg/cm2、時間は0.5〜6時間であることが好ま
しい。
本発明によれば、繊維と複合する金属との両者
が反応してその金属のカーバイド又はけい素化物
等を生成することなく、また、繊維表面のアルミ
ニウム皮膜と複合する金属とが複合時金属間化合
物(TixAl(1―x)、NiyAl(1―y)など)を
形成するので繊維/金属間は強固な結合となる。
得られる無機繊維強化金属複合材料は機械強度
が大となる。
つぎに本発明の実施態様を実施例について説明
するが本発明はこれらによつて限定されるもので
はない。
実施例 1
単繊維径10μのシリコンカーバイド繊維(商品
名:ニカロン、日本カーボン(株)製)の束(単繊
維500本の束)をオートクレーブ中にて720℃に溶
融したアルミニウムに浸漬し、70Kg/cm2の圧力を
加えて平均厚み8μのアルミニウム皮膜を単繊維
表面に形成したシリコンカーバイド繊維束を得
た。
これをチタン箔(厚み50μ)上に繊維体積率約
30%になるように引きそろえてならべさらにそれ
を10層積層して成形型中に充填し、850℃、800
Kg/cm2、1時間成形した。
得られた複合材の特性を第1表に示す。
実施例 2
実施例1で使用したと同一のアルミニウム皮膜
を形成したシリコンカーバイド繊維束をニツケル
箔(厚み50μ)上に繊維体積率約30%になるよう
に引きそろえてならべさらにそれを10層積層して
成形型中に充填し850℃、800Kg/cm2、1時間成形
した。
得られた複合材の特性を第1表に示す。
比較例 1〜2
実施例1に用いたシリコンカーバイド繊維束の
何らアルミニウム皮膜を形成させないもの、およ
び実施例1に用いたオートクレーブ中で平均厚み
12μのアルミニウム皮膜を形成させたもの各々を
チタン箔(厚み50μ)上に繊維体積率約30%にな
るように引きそろえてならべ実施例1の方法によ
り積層、成形したその結果を第1表に示す。
比較例 3〜4
比較例1〜2と使用したと同一のシリコンカー
バイド繊維束をニツケル箔(厚み50μ)上に繊維
体積率約30%になるよう引きそろえてならべ実施
例2と同一方法にて積層、成形したその結果を第
1表に示す。
The present invention relates to an inorganic fiber reinforced metal composite material. Recently, it is lightweight, has excellent heat resistance, and has high compressive strength.
Materials with high mechanical strength such as tensile strength are now required as materials for turbine blade aircraft components and the like. As this type of material, an inorganic fiber-reinforced composite material in which a metal such as titanium or nickel is reinforced with inorganic fibers such as carbon fiber, boron fiber, alumina fiber, or silicon carbide fiber has been proposed. Conventionally, this inorganic fiber-reinforced composite material has been obtained by arranging metal powders such as titanium, nickel, etc. together with inorganic fibers in a mold and heating them. However, the inorganic fiber-reinforced metal composite material obtained by this method cannot be obtained because, for example, when silicon carbide is used as the inorganic fiber and nickel is used as the metal, the nickel is converted into nickel carbide and nickel silicon in the sintering process. The disadvantage is that the strength of the product is reduced and it becomes brittle. Furthermore, when carbon fiber is used as the inorganic fiber and titanium is used as the metal, the titanium in the resulting product is carbonized, so the resulting product has the disadvantage of low strength and brittleness, similar to the above-mentioned composite materials. Furthermore, in the case of composites of boron fibers and alumina fibers, reactions occur at the interface between the fibers and the metal, resulting in insufficient composites. The present inventors conducted research to provide a method for manufacturing an inorganic fiber-reinforced metal composite material that eliminates such drawbacks, and found that inorganic fibers selected from boron fibers, alumina fibers, or silicon carbide fibers, titanium, and nickel. If an aluminum layer of a limited thickness is interposed between the aluminum layer and the alloy mainly composed of these, the time for the metal to be composited to react with the inorganic fibers will be drastically reduced, resulting in the formation of carbides or silicides of the composite metal. The present invention was completed based on the knowledge that an inorganic fiber-metal composite material obtained without the formation of such substances is highly strengthened. The gist of the present invention is to form an aluminum film with a thickness of 0.5 to 10 μm on the surface of inorganic fibers selected from boron fibers, alumina fibers, or silicon carbide fibers, and to combine the inorganic fibers with powdered or foil-like titanium, nickel, and these materials. An inorganic fiber-reinforced metal composite material is produced by arranging the alloys mainly consisting of Alumina fibers and silicon carbide fibers having a fiber diameter of about 5 to 140 μm are preferably used. Titanium, nickel, and alloys based on these are effective as composite metals. A film of aluminum can be formed on inorganic fibers by an ion plating method (vapor deposition method), an impregnation method, or a dipping method. The impregnation method is a method in which inorganic fibers are immersed in molten aluminum and pressurized; in this case, the temperature of the molten metal is
The standard temperature is 700-750℃ and the pressure is 50-100Kg/ cm2 .
When a thin film of low melting point metal is formed on the surface of inorganic fibers under reduced pressure in molten metal, the temperature of the molten metal should be 700 to 750℃.
Perform at 1 torr or less. The thickness of the aluminum film is preferably 0.5 to 10μ. Aluminum and fibers do not form carbide to the extent that a film is formed within this range. The thickness is adjusted by the temperature of the molten metal or, in the case of vapor deposition, the amount of vapor deposition. If the thickness is less than 0.5 μm, the metal and the inorganic fibers will react with each other, which is undesirable, and if the thickness is more than 10 μm, the amount of low melting point metal will increase, which will reduce the adhesive effect of the composite metals, which is undesirable. The composite metal is used in the form of foil (thickness: 50-100μ) or powder (particle size: 40μ or less), and the molding conditions are: heating temperature: 800-1000℃, pressure: 100-100℃.
It is preferable that the pressure is 1000Kg/cm 2 and the time is 0.5 to 6 hours. According to the present invention, the fibers and the metal to be composited do not react to form carbides or silicides of the metal, and the aluminum film on the surface of the fiber and the metal to be composited are bonded between the metals during the composite. Since compounds (TixAl (1-x), NiyAl (1-y), etc.) are formed, the fiber/metal bond becomes strong. The resulting inorganic fiber-reinforced metal composite material has high mechanical strength. Next, embodiments of the present invention will be described with reference to Examples, but the present invention is not limited thereto. Example 1 A bundle (bundle of 500 single fibers) of silicon carbide fibers (product name: Nicalon, manufactured by Nippon Carbon Co., Ltd.) with a single fiber diameter of 10 μm was immersed in aluminum melted at 720°C in an autoclave, and the resulting product was 70 kg. A silicon carbide fiber bundle was obtained by applying a pressure of /cm 2 to form an aluminum film with an average thickness of 8 μm on the surface of the single fibers. This is placed on titanium foil (thickness 50μ) with a fiber volume ratio of approximately
Arrange them so that they are 30%, stack them in 10 layers, fill them in a mold, and heat them at 850℃ and 800℃.
Kg/cm 2 and molded for 1 hour. Table 1 shows the properties of the composite material obtained. Example 2 Silicon carbide fiber bundles coated with the same aluminum film as used in Example 1 were arranged on a nickel foil (thickness 50μ) so that the fiber volume ratio was approximately 30%, and then 10 layers were stacked. The mixture was filled into a mold and molded at 850° C. and 800 kg/cm 2 for 1 hour. Table 1 shows the properties of the composite material obtained. Comparative Examples 1-2 Silicon carbide fiber bundles used in Example 1 that do not form any aluminum film, and average thickness in the autoclave used in Example 1
Each of the aluminum films on which a 12 μm thick aluminum film was formed was arranged on a titanium foil (thickness: 50 μm) so that the fiber volume ratio was approximately 30%, and then laminated and molded using the method of Example 1. The results are shown in Table 1. show. Comparative Examples 3-4 The same silicon carbide fiber bundles as those used in Comparative Examples 1-2 were arranged on a nickel foil (thickness 50μ) so that the fiber volume percentage was about 30%, and the same method as in Example 2 was used. The results of lamination and molding are shown in Table 1.
【表】【table】
【表】
実施例 3〜6
第2表に示すそれぞれの繊維に第2表に示す条
件で数々の厚みのアルミニウム皮膜を行つた。
これらの繊維をTi粉末(40μ以下)、Ni粉末
(40μ以下)とそれぞれ積層して第2表に示す特
性の複合材を得た。[Table] Examples 3 to 6 Aluminum coatings of various thicknesses were applied to each of the fibers shown in Table 2 under the conditions shown in Table 2. These fibers were laminated with Ti powder (40 μm or less) and Ni powder (40 μm or less) to obtain a composite material with the characteristics shown in Table 2.
【表】
実施例 7〜8
実施例1で使用したと同一のアルミニウム皮膜
を形成したシリコンカーバイド繊維束をTi―6Al
―4Vチタン合金箔(厚み100μ)およびNi―Cr合
金(Inconel×―550)箔(厚み100μ)上に繊維体
積率約35%になるよう各々引きそろえてならべこ
れを各々10層積層して850℃、1000Kg/cm2、1時間
成形して、チタン合金複合材およびニツケル合金
複合材を得た。
その引張り張度はチタン合金複合材150Kg/mm2、
ニツケル合金複合材155Kg/mm2であつた。[Table] Examples 7 to 8 Silicon carbide fiber bundles coated with the same aluminum film as used in Example 1 were treated with Ti-6Al.
-4V titanium alloy foil (thickness 100μ) and Ni-Cr alloy (Inconel x -550) foil (thickness 100μ) are each lined up so that the fiber volume percentage is approximately 35%, and 10 layers each are laminated to form 850. C. and 1000 Kg/cm 2 for 1 hour to obtain a titanium alloy composite material and a nickel alloy composite material. Its tensile strength is titanium alloy composite material 150Kg/mm 2 ,
The nickel alloy composite material was 155Kg/ mm2 .
Claims (1)
形成した、ボロン繊維、アルミナ繊維、又はシリ
コンカーバイド繊維から選ばれた無機繊維と厚み
50〜100μの箔状又は粒径40μ以下の粉末状のチタ
ン、ニツケル及びこれらを主体とした合金とを成
形型内に配列し、ついで加圧下で加熱成形するこ
とを特徴とする無機繊維強化金属複合材料の製造
法。1. Inorganic fibers selected from boron fibers, alumina fibers, or silicon carbide fibers with an aluminum coating of 0.5 to 10μ thick on the surface.
An inorganic fiber-reinforced metal characterized by arranging titanium, nickel, or an alloy mainly composed of these in a foil shape of 50 to 100 μm or in powder form with a particle size of 40 μm or less in a mold, and then heat-forming it under pressure. Method of manufacturing composite materials.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP19083381A JPS5893834A (en) | 1981-11-30 | 1981-11-30 | Manufacture of inorganic fiber reinforced metallic composite material |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP19083381A JPS5893834A (en) | 1981-11-30 | 1981-11-30 | Manufacture of inorganic fiber reinforced metallic composite material |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS5893834A JPS5893834A (en) | 1983-06-03 |
| JPH0122331B2 true JPH0122331B2 (en) | 1989-04-26 |
Family
ID=16264517
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP19083381A Granted JPS5893834A (en) | 1981-11-30 | 1981-11-30 | Manufacture of inorganic fiber reinforced metallic composite material |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS5893834A (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH02111427U (en) * | 1989-02-23 | 1990-09-06 |
Families Citing this family (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS609568A (en) * | 1983-06-29 | 1985-01-18 | Toray Ind Inc | Production of fiber-reinforced composite metallic material |
| JPH07818B2 (en) * | 1985-11-20 | 1995-01-11 | 株式会社日立製作所 | Method for producing metal matrix-fiber composite material |
| US5660923A (en) * | 1994-10-31 | 1997-08-26 | Board Of Trustees Operating Michigan State University | Method for the preparation of metal matrix fiber composites |
| US6086688A (en) * | 1997-07-28 | 2000-07-11 | Alcan International Ltd. | Cast metal-matrix composite material and its use |
Family Cites Families (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS5334083A (en) * | 1976-09-10 | 1978-03-30 | Matsushita Electric Works Ltd | Time-multi multiplex transmission system |
-
1981
- 1981-11-30 JP JP19083381A patent/JPS5893834A/en active Granted
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH02111427U (en) * | 1989-02-23 | 1990-09-06 |
Also Published As
| Publication number | Publication date |
|---|---|
| JPS5893834A (en) | 1983-06-03 |
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