JPH0483833A - Particle dispersed composite and its manufacture - Google Patents
Particle dispersed composite and its manufactureInfo
- Publication number
- JPH0483833A JPH0483833A JP20049890A JP20049890A JPH0483833A JP H0483833 A JPH0483833 A JP H0483833A JP 20049890 A JP20049890 A JP 20049890A JP 20049890 A JP20049890 A JP 20049890A JP H0483833 A JPH0483833 A JP H0483833A
- Authority
- JP
- Japan
- Prior art keywords
- composite
- ceramic particles
- molten metal
- preform
- composite material
- 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
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- Manufacture Of Alloys Or Alloy Compounds (AREA)
Abstract
Description
【発明の詳細な説明】
a、 産業上の利用分野
本発明は複合化率が部分的に異なる粒子分散型複合材料
とその製造方法に関する。DETAILED DESCRIPTION OF THE INVENTION a. Field of Industrial Application The present invention relates to a particle-dispersed composite material having partially different composite ratios and a method for producing the same.
b、 従来の技術 複合材料に関し、次のような従来技術が知られている。b. Conventional technology Regarding composite materials, the following conventional techniques are known.
たとえば、SiCやCなどの繊維やウィスカーでプリフ
ォームを製作し、これを金型内にセットしたあと、A1
合金などの溶湯を注いで、プリフォームに加圧含浸させ
ることで複合材料(FRM)とする方法である。For example, after making a preform using fibers such as SiC or C or whiskers and setting it in a mold,
This is a method of making a composite material (FRM) by pouring molten metal such as an alloy and impregnating it into a preform under pressure.
また、5iCJpCなどの粒子を、完全溶融または部分
溶融の溶湯に添加し、これに機械的撹拌を与えて複合材
料(MMC)とするコンポキャスト法がある。There is also a composite casting method in which particles such as 5iCJpC are added to a completely or partially melted molten metal and mechanically stirred to form a composite material (MMC).
さらにSiCやCなどの粒子とAI!合金等の粉末とを
混合し、静水圧々縮や熱間押出し、または焼結等によっ
て複合材料を製造する方法(粉末冶金法)が広くおこな
われている。Furthermore, particles such as SiC and C and AI! A widely used method (powder metallurgy method) is to mix powders such as alloys and produce composite materials by hydrostatic compression, hot extrusion, sintering, or the like.
また、SiCやCなどの粒子とAf金合金の粉末を混合
し、これに熱間で機械的撹拌を与えて、合金粉末中にS
iCやCなどの粒子を練込み、粒子分散複合材料とする
方法(メカニカルアロイング法)がある。In addition, by mixing particles such as SiC or C with powder of Af gold alloy and applying hot mechanical agitation, S
There is a method (mechanical alloying method) in which particles such as iC and C are kneaded into a particle-dispersed composite material.
C1発明が解決しようとする課題
SiCやCなどの繊維やウィスカーは高価であり、また
、これらを用いておこなうプリフォームの製作には手間
がかかり、製品コストが高くなるという欠点がある。C1 Problems to be Solved by the Invention Fibers and whiskers such as SiC and C are expensive, and manufacturing a preform using them is labor-intensive, resulting in high product costs.
また、前記コンポキャスト法においては、溶湯に添加す
る粒子に濡れ性の良いものを用いても、むらなく均一に
分散させるためには、溶湯に対する添加割合は20w
t%が上限であり、これ以上の添加は困難である。In addition, in the above-mentioned composite casting method, even if particles with good wettability are added to the molten metal, the addition ratio to the molten metal must be 20w in order to evenly and uniformly disperse the particles.
The upper limit is t%, and it is difficult to add more than this.
さらに粉末冶金に用いる合金粉末は製造が難しく、その
ため高価であり、また複合材料として完成するまでの工
程が多くかかるという欠点がある。Furthermore, the alloy powder used in powder metallurgy is difficult to manufacture and therefore expensive, and has the disadvantage that it takes many steps to complete it as a composite material.
そして押出しの方法で製造するため、単純形状に限られ
てしまうという問題がある。Since it is manufactured by extrusion, there is a problem in that it is limited to simple shapes.
また、メカニカルアロイング法に用いる合金粉末は、前
述のように高価であり、混合割合も50wt%程度が限
度であり、製品製造には押出し工程が必要で、前記粉末
冶金と同様な問題点がある。In addition, the alloy powder used in the mechanical alloying method is expensive as mentioned above, the mixing ratio is limited to about 50 wt%, and an extrusion process is required to manufacture the product, which has the same problems as the powder metallurgy. be.
一方、複合化率の異なる複合材料の製造に関しては未だ
提案されたものがほとんどない。On the other hand, there have been few proposals regarding the production of composite materials with different composite ratios.
本発明は、前記事情に鑑みてなされたもので前記問題点
を解消してなる複合化率の異なる粒子分散型複合材料と
、その製造方法を擾供することを目的とする。The present invention has been made in view of the above circumstances, and an object of the present invention is to provide a particle-dispersed composite material having different composite ratios, which solves the above problems, and a method for producing the same.
d、 illを解決するための手段
前記目的に添い、本発明は、AlまたはMg合金をマト
リックスとし、高率の複合化部分と、それより低率の複
合化部分と更に低率の複合化部分とを有する粒子分散型
複合材料とすることによって前記課題を解消した。Means for Solving Problems d and ill In accordance with the above object, the present invention uses Al or Mg alloy as a matrix, and provides a composite portion with a high ratio, a composite portion with a lower ratio, and a composite portion with an even lower ratio. The above problem was solved by creating a particle-dispersed composite material having the following.
さらに本発明はセラミックス粒子の予成形体に対し、セ
ラミックス粒子を均一に分散してなるマトリックス合金
の溶湯を注湯して加圧し、複合化率の相違する部分を形
成することによって前記課題を解消した。Furthermore, the present invention solves the above problem by pouring a molten metal of a matrix alloy in which ceramic particles are uniformly dispersed into a preformed body of ceramic particles and pressurizing it to form parts with different composite ratios. did.
以下、本発明について図面を参照しながら詳細に説明す
る。Hereinafter, the present invention will be explained in detail with reference to the drawings.
本発明においては複合用の添加材料として、セラミック
ス粒子を用いる。セラミック粒子としては、たとえばS
iC,A l toy、 5jJa+ TiC,WC+
Zr0z、 BN、 Cまたはこれらの混合粒子を用
いる。In the present invention, ceramic particles are used as the additive material for the composite. As ceramic particles, for example, S
iC, Al toy, 5jJa+ TiC, WC+
Zr0z, BN, C or a mixture of these particles is used.
このセラミックスの粒子径(平均粒子径)は0.01〜
30μ−の範囲のものを用いる。粒子径が0.01μ−
未満のものは製造が難しく高価であり、かつ均一な複合
化が困難である。また、粒子径が30tIIlを越える
と製造する複合材料の強度の改善が期待できない。The particle size (average particle size) of this ceramic is 0.01~
A material in the range of 30 μ- is used. Particle size is 0.01 μ-
Anything less than this is difficult and expensive to manufacture, and it is difficult to form a uniform composite. Furthermore, if the particle size exceeds 30tIII, no improvement in the strength of the composite material to be produced can be expected.
マトリックス合金としては、八2またはM、の合金を用
いる。たとえば、JIS AC4C,JIS MC7な
どである。As the matrix alloy, an alloy of 82 or M is used. For example, JIS AC4C, JIS MC7, etc.
まず、セラミックス粒子(たとえばSiC99wt%+
BN1wt%を用いる。これは高硬度のSiCと潤滑性
を備えたBNとによって耐摩耗性の優れた複合材料とな
る)を、水分の除去と、後に添加する合金溶湯が浸入し
易いように、300〜900℃の温度で予熱する。この
予熱温度が300°C未満の場合であると、接触した溶
湯がすぐ凝固してしまうためセラミックス粒子間へ十分
浸透しない、また、900℃を越えて予熱すると、接触
した溶湯が凝固するまでに時間がかかり、一部成分と反
応して化合物などをつくるため好ましくない。First, ceramic particles (for example, SiC99wt%+
BN1wt% is used. This is a composite material with excellent wear resistance due to the high hardness of SiC and BN with lubricating properties. Preheat to temperature. If the preheating temperature is less than 300°C, the molten metal in contact will solidify immediately and will not penetrate between the ceramic particles sufficiently.If the preheating temperature exceeds 900°C, the molten metal in contact will solidify quickly. It is undesirable because it takes time and reacts with some components to form compounds.
次に、第1図(a)に示すように温度100〜400°
Cに加熱しである金型2内に、セラミックス粒子1を収
容したあと、同図(b)に示すように上パンチ3と下バ
ンチ5とを用いて、1〜100100O0/ c4の圧
力P、で加圧し、セラミックス粒子の予成形体4を形成
する。ここで圧力P、が1kgf/cj未溝の場合は予
成形体に強度かえられず、後の工程で変形したり、壊れ
たりするおそれがある。一方、圧力Pがloo00kg
f/cdを越えると、粒子密度が高くなりすぎたり、後
の工程で添加する溶湯が浸透しにくくなり、また、金型
自体の強度上の問題も発生する。Next, as shown in Figure 1(a), the temperature is 100 to 400°.
After placing the ceramic particles 1 in the mold 2 heated to C, as shown in FIG. Pressure is applied to form a preformed body 4 of ceramic particles. If the pressure P is 1 kgf/cj without a groove, the strength of the preformed body will not be increased, and there is a risk that it will be deformed or broken in a later process. On the other hand, the pressure P is loo00kg
If f/cd is exceeded, the particle density becomes too high, the molten metal added in a later step becomes difficult to penetrate, and problems arise in terms of the strength of the mold itself.
一方、別途にマトリックスとする合金を用意する。この
マトリックス合金はA!金合金たはqg合金であって、
セラミックス粒子を均一に分散してなる複合材料を用い
る。On the other hand, an alloy to be used as a matrix is separately prepared. This matrix alloy is A! A gold alloy or a QG alloy,
A composite material made of uniformly dispersed ceramic particles is used.
用いるへ2合金としては、たとえばJIS AC8Aが
あり、Mg合金としては、たとえばJIS ?IC8が
ある。Examples of the alloy used include JIS AC8A, and examples of the Mg alloy include JIS AC8A. There is IC8.
また複合材料に分散しているセラミックス粒子としでは
、前記成形体を成形したものと同一素材、たとえばSi
C99wt%+BN 1 wt%の粒子、または其他の
、たとえばSiC,A l 203. si3+14.
TiC,WC。Furthermore, the ceramic particles dispersed in the composite material are made of the same material as that used to form the molded body, such as Si.
C99wt%+BN1 wt% particles, or others such as SiC, Al 203. si3+14.
TiC, W.C.
ZrO□、 BN、 C1あるいは、これらの混合粒
子を用いる。また、これらセラミックスの粒子径も前記
成形体に用いたものとほぼ同じ範囲のものを用いる。ZrO□, BN, C1 or a mixture of these particles is used. Furthermore, the particle diameter of these ceramics is also within approximately the same range as that used for the molded body.
このようなセラミックス粒子を均等に分散してなる複合
材料6を、650〜850°Cの温度で加熱溶解し、こ
の溶湯6を第1図(C)に示すように前記成形体4の上
部に給湯する。A composite material 6 made by uniformly dispersing such ceramic particles is heated and melted at a temperature of 650 to 850°C, and the molten metal 6 is poured onto the top of the molded body 4 as shown in FIG. 1(C). Supply hot water.
なお、この溶解温度は、凝固が早すぎたり、高温となり
すぎガス等の吸入がないように適度の温度範囲とする。The melting temperature is set within an appropriate temperature range so as not to cause solidification to occur too quickly or to a high temperature that may cause inhalation of gas, etc.
たとえば前記材料の場合では650゜未満では凝固が早
すぎ、850°Cを越えると11.、 N。For example, in the case of the above-mentioned materials, if the temperature is less than 650°C, solidification will be too rapid, and if the temperature exceeds 850°C, the temperature will be 11. ,N.
などのガスの吸入が多くなり好ましくない。This is undesirable as it causes a lot of inhalation of gases such as.
次に、同図(d)に示すように上バンチ7によって10
0〜100100O0/ c4の圧力P2で加圧し、溶
湯6を予成形体4に浸透させる。この場合、圧力P2が
100kgf / ci未溝の場合では溶湯の予成形体
内への浸透が充分ではなく 、100100O0/C4
を越える加圧は実質的に必要がない。Next, as shown in the same figure (d), 10
The molten metal 6 is permeated into the preform 4 by applying pressure P2 of 0 to 100100 O0/c4. In this case, when the pressure P2 is 100 kgf/ci and there is no groove, the penetration of the molten metal into the preformed body is insufficient, and 100100O0/C4
There is virtually no need to pressurize in excess of this amount.
前記加圧によって、セラミックス粒子を含む溶湯は成形
体4内に浸透し、得られた複合材料はA。By applying the pressure, the molten metal containing ceramic particles permeates into the molded body 4, and the resulting composite material is A.
B、Cの各部でそれぞれ異なった複合化率のものかえら
れる。すなわち、A部はセラミックス粒子を含む溶湯6
の組成のものがそのままに、0部は最も複合化率が高い
ものが(50〜90−t%)、B部はマトリックス合金
がC部内へ移動して結果的にセラミックス粒子が多くな
った部分で、0部に次いで複合化率が高くなる(10〜
70−t%)。すなわち複合化率は常にC>B>Aとな
った粒子分散型複合材料かえられる。Each part of B and C can be changed to a different compounding rate. That is, part A is the molten metal 6 containing ceramic particles.
The composition remains the same, part 0 is the one with the highest composite rate (50-90-t%), and part B is the part where the matrix alloy has moved into part C, resulting in an increase in ceramic particles. The compounding rate is the second highest after 0 parts (10~
70-t%). That is, the composite ratio is always changed to a particle-dispersed composite material in which C>B>A.
第2図は4サイクルエンジン用バルブリフターに適用し
た例を示し、SiC99wt%+BN l wt%から
なるセラミックス粒子101を800°Cに予熱し、こ
れを第2図(a) (b)に示すように300℃に加熱
した金型102内へ投入して上パンチ103 と下パン
チ105との間で、圧力PIを100100O/cjと
して加圧して成形体104を成形する。Fig. 2 shows an example of application to a valve lifter for a four-stroke engine. Ceramic particles 101 consisting of 99 wt% SiC + 1 wt% BN are preheated to 800°C, and the particles are heated as shown in Fig. 2 (a) and (b). The molded product 104 is then put into a mold 102 heated to 300° C. and pressed between an upper punch 103 and a lower punch 105 at a pressure PI of 100,100 O/cj to form a molded product 104.
次にJIS AC4Cをマトリックス合金とし、SiC
99wt%+BN l wt%を分散してなる複合材料
を用い、これを750°Cに加熱溶解してなる溶湯10
6を、同図(C)に示すように金型102内の成形体1
04上に給湯し、上パンチ107によって同図(ロ)に
示すように1000 kg f / c4の圧力P2で
加圧した。Next, using JIS AC4C as the matrix alloy, SiC
Molten metal 10 made by heating and melting this at 750°C using a composite material made by dispersing 99 wt% + BN l wt%
6 into the molded body 1 in the mold 102 as shown in the same figure (C).
04 and pressurized with the upper punch 107 at a pressure P2 of 1000 kgf/c4 as shown in FIG.
冷却後、脱型して得られた製品は頂部のカム摺動部に当
る0部は耐摩耗性と潤滑性に最も優れた性質を備え、側
面のB部はこれに次ぎ、A部は通常の粒子分散型の複合
材料のもつ性質のものが得られた。After cooling, the product obtained by demolding has the best properties in terms of wear resistance and lubricity, with part 0, which corresponds to the cam sliding part at the top, having the best properties in terms of wear resistance and lubricity. The properties of a particle-dispersed composite material were obtained.
第3図は本発明に係る複合材料の金属組織を示す写真で
、平均粒子径1μ讃のSiC粒子を、P、圧力1001
00O/cdで加圧成形した予成形体に、八C4Cに平
均粒子径13μ−のSiC粒子を10−t%複合してな
る溶湯を注いで加圧したものを示す、同図(a)はA、
B、Cの各部を含む全体の金属組織を、同図(b)はA
部を拡大したものを、同図(C)はB部と0部及びその
境界部分を拡大したものを、同図(ロ)は0部を拡大し
たものを夫々示す。これら写真から各部の複合状態が明
瞭に判る。Figure 3 is a photograph showing the metallographic structure of the composite material according to the present invention.
Figure (a) shows a preformed body pressure-formed at 000/cd, which was then pressurized with a molten metal made of a 10-t% composite of 8C4C and SiC particles with an average particle size of 13μ. A,
Figure (b) shows the entire metal structure including parts B and C.
The figure (C) shows an enlarged view of the B part, the 0 part and the boundary between them, and the figure (B) shows an enlarged view of the 0 part. These photos clearly show the composite condition of each part.
e、 発明の効果
以上のように本発明によれば、セラミックス粒子の複合
化率が同−材料内で異なっている粒子分散型複合材料が
比較的簡単な鋳造方法を用いて製造でき、また任意形状
の材料や製品かえられる。e. Effects of the Invention As described above, according to the present invention, a particle-dispersed composite material in which the composite ratio of ceramic particles is different within the same material can be manufactured using a relatively simple casting method, and can be made by any method. The material and product shape can be changed.
そして全体的に硬さ、耐熱性、耐摩耗性、剛性、疲労強
度に優れ、部分的に、かつ段階的にこれら性質のより優
れた部分を有する複合化率の高い複合材料かえられる。Then, a composite material with a high composite ratio, which has excellent hardness, heat resistance, abrasion resistance, rigidity, and fatigue strength as a whole, and which has parts that are superior in these properties in parts and in stages, can be used.
第1図(a)5らJ、 (C)、 (d)は本発明に係
る粒子分散型複合材料の製造要領を説明する図、第2図
は同じく他の実施例に係る製造要領を説明する図、第3
図(a) 、 (b) 、 (C) 、■は本発明に係
る複合材料の金属組織の写真で、同図(a)は全体を示
し、同図(b)はA部を、同図(C)はB部と0部を、
同図(d)は0部を夫々拡大したものを示す。
1.101 ・・・セラミックス粒子、2.102・・
・金型、 4.104・・・予成形体、6.106
・・・溶湯。
第:3
(a)
×5
(C)
(b)
(d)
X 4LJ(JFigures 1 (a), (C), and (d) are diagrams explaining the manufacturing procedure of the particle-dispersed composite material according to the present invention, and Figure 2 similarly explains the manufacturing procedure according to another example. figure, 3rd
Figures (a), (b), (C), and ■ are photographs of the metal structure of the composite material according to the present invention. Figure (a) shows the whole, Figure (b) shows part A, and (C) is part B and part 0,
The same figure (d) shows the enlarged version of the 0 part. 1.101... Ceramic particles, 2.102...
・Mold, 4.104... Preformed body, 6.106
...Molten metal. No. 3 (a) ×5 (C) (b) (d) X 4LJ (J
Claims (1)
合化部分と、それより低率の複合化部分と、更に低率の
複合化部分とを有する粒子分散型複合材料。 2)セラミックス粒子の予成形体に対し、セラミックス
粒子を均一に分散してなるマトリックス合金の溶湯を注
湯して加圧し、複合化率の相違する部分を形成すること
を特徴とする粒子分散型複合材料の製造方法。[Scope of Claims] 1) A particle-dispersed composite material that uses Al or Mg alloy as a matrix and has a composite portion with a high percentage, a composite portion with a lower percentage, and a composite portion with an even lower percentage. 2) A particle dispersion type characterized in that a molten metal of a matrix alloy made of ceramic particles uniformly dispersed is poured into a preformed body of ceramic particles and pressurized to form parts with different composite ratios. Method of manufacturing composite materials.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP20049890A JPH0483833A (en) | 1990-07-27 | 1990-07-27 | Particle dispersed composite and its manufacture |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP20049890A JPH0483833A (en) | 1990-07-27 | 1990-07-27 | Particle dispersed composite and its manufacture |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| JPH0483833A true JPH0483833A (en) | 1992-03-17 |
Family
ID=16425323
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP20049890A Pending JPH0483833A (en) | 1990-07-27 | 1990-07-27 | Particle dispersed composite and its manufacture |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPH0483833A (en) |
-
1990
- 1990-07-27 JP JP20049890A patent/JPH0483833A/en active Pending
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