JPS6270041A - Manufacture of compounded ceramics - Google Patents
Manufacture of compounded ceramicsInfo
- Publication number
- JPS6270041A JPS6270041A JP21123585A JP21123585A JPS6270041A JP S6270041 A JPS6270041 A JP S6270041A JP 21123585 A JP21123585 A JP 21123585A JP 21123585 A JP21123585 A JP 21123585A JP S6270041 A JPS6270041 A JP S6270041A
- Authority
- JP
- Japan
- Prior art keywords
- ceramics
- zro2
- layer
- al2o3
- ceramic powder
- 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
Landscapes
- Laminated Bodies (AREA)
Abstract
(57)【要約】本公報は電子出願前の出願データであるた
め要約のデータは記録されません。(57) [Summary] This bulletin contains application data before electronic filing, so abstract data is not recorded.
Description
【発明の詳細な説明】
〔産業上の利用分野〕
本発明は、複数の性質ケもつセラミックス七複合化した
抗折強度の大きい複合化セラミックスの製造法に関する
。DETAILED DESCRIPTION OF THE INVENTION [Field of Industrial Application] The present invention relates to a method for producing a composite ceramic having a high flexural strength, which is a composite of seven ceramics having a plurality of properties.
セラミックスは、その耐熱性、高剛性、耐摩耗性あるい
は耐食性などの点で、在来の金属材料ケ超え几すぐれた
特性2有する几め、構造用材料としての使用が広い分野
で試みられるようになってきた。一般にセラミックスは
、金属に比して欠陥の存在に対する感受性が著しく高く
。Ceramics have superior properties2 to conventional metal materials in terms of heat resistance, high rigidity, wear resistance, and corrosion resistance, and their use as structural materials has begun to be attempted in a wide range of fields. It has become. In general, ceramics are significantly more sensitive to the presence of defects than metals.
圧縮応力に対しては強い抵抗?示すが、引張応力に対し
ては弱く、小さな力でも破壊する率が高い。その程度は
、セラミックスの材質によっても異る。例えば、 A
l2O,は、低応力で破壊し。Strong resistance to compressive stress? However, it is weak against tensile stress and has a high probability of breaking even with a small force. The degree also varies depending on the ceramic material. For example, A
l2O, breaks at low stress.
耐熱衝撃性も劣るが、同じ酸化物系でもZrO2゜特に
1部分安定化ジルコニア(以下PSZと略す)は、高応
力下でも使用可能で、セラミックスの中では靭性も大き
く、近年広範囲に使用されるようになってきた。 ゛
〔発明が解決しようとする問題点〕
しかし、ジルコニア系セラミックスは、非常に高価であ
るという欠点がある。また焼成したPSZと他の安価な
セラミックス焼成体r接合するにしても、その接合が難
しく、更にコストアツブに継がる傾向があった。また、
粉体プレス時に成形ダイス内で9両者ケ1層目2層目と
して充填し1 プレスする方法も考えられるが、収縮率
の違いにより、焼成時に剥離し、接合できなかった。Although the thermal shock resistance is inferior, ZrO2゜particularly partially stabilized zirconia (hereinafter abbreviated as PSZ) can be used even under high stress and has high toughness among ceramics, so it has been widely used in recent years. It's starting to look like this. [Problems to be Solved by the Invention] However, zirconia ceramics have the drawback of being extremely expensive. Furthermore, even if the fired PSZ and other inexpensive fired ceramic bodies were to be joined together, the joining would be difficult and would also tend to be costly. Also,
A method of filling the first and second layers of both layers in a molding die during powder pressing and pressing could be considered, but due to the difference in shrinkage rate, they peeled off during firing and could not be bonded.
本発明は、上記従来技術の不具合に鑑みてなされたもの
で1種々特性にすぐれるが価格の高いジルコニア系セラ
ミックスと価格の安いアルミナ系セラミックスとケ複合
化して両者の長所ケ兼ね備え、しかも両者の接合強度が
充分な複合化セラミックスの製造法勿提供することケ目
的とする。The present invention was made in view of the above-mentioned problems of the prior art, and combines zirconia ceramics, which have excellent properties but are expensive, and alumina ceramics, which are cheap, to combine the advantages of both. The object of the present invention is to provide a method for manufacturing composite ceramics with sufficient bonding strength.
そのため本発明は、成形ダイス内の一側に焼成助剤r添
加し几アルミナ系セラミックス粉末層ケ配し、他側に焼
成助剤ケ添加しtジルコニア系セラミックス粉末層を配
して、該2粉末層間にアルミナ系セラミックス粉末及び
ジルコニア系セラミックス粉末の混合層21層以上設け
て、プレス成形し、その後加熱して焼成することケ特徴
とする複合化セラミックスの製造法を要旨とする。Therefore, in the present invention, a firing aid R is added and a zirconia ceramic powder layer is arranged on one side of the forming die, and a firing aid R is added and a zirconia ceramic powder layer is arranged on the other side. The gist of this invention is a method for producing composite ceramics characterized by providing 21 or more mixed layers of alumina-based ceramic powder and zirconia-based ceramic powder between powder layers, press-molding, and then heating and firing.
次に0本発明の製造方法?第1図にもとづき説明する。 Next is the manufacturing method of the present invention? This will be explained based on FIG.
第1図は、プレス成形ダイス内での状態ケ示す縦断側面
図である。本発明は、Al2O3゜ZrO2及び1両者
?混合した属から成る。この内、混合1層?設けること
が本発明の最大のポイントとなる。Al2O3及びZr
O7は1それぞれ400〜1000kgf/d程度の圧
力で成形される。FIG. 1 is a longitudinal sectional side view showing the state inside the press molding die. The present invention relates to Al2O3゜ZrO2 and 1? Consists of mixed genera. One of these is a mixed layer? Providing this is the most important point of the present invention. Al2O3 and Zr
Each O7 is molded at a pressure of about 400 to 1000 kgf/d.
成形圧一定(成形圧600kg肩)の場合、 155
0°C焼成での収縮率は1. Ad20318%、Z
rO□25%程度である。従って前記従来法で説明した
様に。When molding pressure is constant (molding pressure 600kg shoulder), 155
The shrinkage rate when fired at 0°C is 1. Ad20318%, Z
The rO□ is about 25%. Therefore, as explained in the conventional method above.
A l 203及びZrO2に二層プレスし友のでは、
境界から剥離し、製品が得られない。混合層は。In case of double layer pressing on Al 203 and ZrO2,
It peels off from the border and no product is obtained. The mixed layer is.
この収縮率の違いによる剥離防止ケ目的としたもので、
この層によって収縮率の差?吸収する。The purpose is to prevent peeling due to this difference in shrinkage rate.
Is there a difference in shrinkage rate depending on this layer? Absorb.
第1図では、Al2O3:ZrO2ノ体積比t1:1と
した例を示しているが、製品、特に厚肉品では。FIG. 1 shows an example in which the volume ratio of Al2O3:ZrO2 is t1:1, but this is not the case for products, especially thick-walled products.
比率?除々に替えて行く、多層成形ケ行なう場合もある
。尚、 Al2O3は、焼成助剤としてM、yO’i
0.5重量%、 ZrO2はY20s k 3 mo
13%それぞれ添加したものが好適である。この状態
でプレス成形した後、望ましくは、 xsoO〜16
00℃の範囲で大気焼成ケ行なう。1500’C未満で
は。ratio? In some cases, multi-layer molding is performed, with gradual changes. In addition, Al2O3 is M, yO'i as a sintering aid.
0.5% by weight, ZrO2 is Y20s k 3 mo
It is preferable to add 13% of each. After press molding in this state, preferably xsoO~16
Calcination is carried out in the atmosphere at a temperature of 0.000C. Below 1500'C.
ZrO2は十分に緻密化するが、 Al2O3は殆んど
焼結されない。また、 1600℃ ?越えると。ZrO2 is sufficiently densified, but Al2O3 is hardly sintered. Also, 1600℃? If you cross it.
Al2O3は緻密化するが、’ZrO2は粒成長ケ起こ
しZrO2の最大の特徴である高強度、高靭性の利点が
損われがちである。Although Al2O3 is densified, ZrO2 tends to cause grain growth and the advantages of high strength and high toughness, which are the most important characteristics of ZrO2, tend to be lost.
〔第1実施例〕
原料粉末として、平均粒径0.5 a m k有するA
l2O3ニMJO0,5wt%添加の粉末と、 Zr
O2はY2O323mo1%添加したものケ用意し、こ
れらの原料上Al2O3系100voJ%、Al2O3
:ZrO2系50 : 50 VO1%、 ZrO2
系100vo1%に成形し、成形圧は400kgf/7
とした。その後成形体全乾燥し、大気中: 1550°
Cで5Hr保持し。[First Example] A having an average particle size of 0.5 a m k as a raw material powder
Powder added with l2O3niMJO0.5wt%, and Zr
O2 was prepared by adding 23 mo1% of Y2O3, and on these raw materials, 100 voJ% of Al2O3 system, Al2O3
:ZrO2-based 50: 50 VO1%, ZrO2
The system is molded to 100vo1%, and the molding pressure is 400kgf/7
And so. After that, the molded body is completely dried in the atmosphere: 1550°
Hold at C for 5 hours.
複合セラミックス會製造した。この結果得られた本実施
例の複合化セラミックスの密度は4.92El/cf、
抗折力は50ゆf/m%程度であった。Manufactured by composite ceramics company. The density of the composite ceramic of this example obtained as a result was 4.92 El/cf,
The transverse rupture strength was approximately 50 Yuf/m%.
〔第2実施例〕 原料粉末として、実施例1で用い友と同じ。[Second example] The raw material powder was the same as that used in Example 1.
平均粒径0.5μmk有するAl2O3に、 My○0
.5 W t%添加の粉末と、 ZrO2はY2O3
23mo71!%添加しtものケ用意し、これらの原料
ケAl2O3系100voj%、Al2O3: ZrO
2系75:25. 50:50.25ニア5vo6%、
ZrO2系100vo6%の多層に成形した。成形
圧は40okgf肩とした。My○0 in Al2O3 with an average particle size of 0.5μmk
.. 5 W t% added powder and ZrO2 is Y2O3
23mo71! % addition, prepare these raw materials Al2O3 system 100voj%, Al2O3: ZrO
2 series 75:25. 50: 50.25 near 5vo 6%,
It was molded into a multilayer of ZrO2-based 100vo6%. The molding pressure was set at 40 kgf.
その後乾燥し、大気中1550°Cで5Hr 保持し
。Thereafter, it was dried and kept at 1550°C for 5 hours in the atmosphere.
複合セラミックス?製造した。この結果得られた本実施
例の複合化セラミックスの密度は。Composite ceramics? Manufactured. The density of the composite ceramic of this example obtained as a result is as follows.
4.98.9/cn(抗折力は60 kg f/n+n
t程度であツタ。4.98.9/cn (transverse rupture strength is 60 kg f/n+n
Ivy at about t.
本発明の方法により製造しり複合化セラミックスは1両
部材の接合が良好であるから、A1203とZrO2の
もつ長所ケ有効に活用することができる。従ってZrO
2の高価な欠点2Ag、、o3の安価なセラミックスで
補う事により、きわめて広範囲の分野に適用することが
できる。Since the composite ceramic produced by the method of the present invention has good bonding between two parts, the advantages of A1203 and ZrO2 can be effectively utilized. Therefore, ZrO
By compensating for the expensive disadvantage of 2 with the inexpensive ceramics of 2Ag, .o3, it can be applied to an extremely wide range of fields.
第1図は本発明の一実施例としての複合セラミックスの
成形状況の説明図である。
1・・・成形ダイス、2・・・成形体、2a・・・Al
2O3系100voJ%の層、 2 b ・−a12
o3: ZrO2系50: 50 vod%の層、
3 c−ZrO,、系100vo/%の層FIG. 1 is an explanatory diagram of a molding situation of a composite ceramic as an example of the present invention. 1... Molding die, 2... Molded body, 2a... Al
2O3 system 100voJ% layer, 2 b ・-a12
o3: ZrO2-based 50: 50 vod% layer,
3 c-ZrO, system 100vo/% layer
Claims (1)
ラミックス粉末層を配し、他側に焼成助剤を添加したジ
ルコニア系セラミックス粉末層を配して、該2粉末層間
にアルミナ系セラミックス粉末及びジルコニア系セラミ
ックス粉末の混合層を設けて、プレス成形し、その後加
熱して焼成することを特徴とする複合化セラミックスの
製造法。An alumina ceramic powder layer to which a firing aid has been added is arranged on one side of the forming die, a zirconia ceramic powder layer to which a firing aid has been added to the other side, and the alumina ceramic powder is placed between the two powder layers. A method for producing composite ceramics, characterized in that a mixed layer of zirconia-based ceramic powder is provided, press-molded, and then heated and fired.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP21123585A JPS6270041A (en) | 1985-09-25 | 1985-09-25 | Manufacture of compounded ceramics |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP21123585A JPS6270041A (en) | 1985-09-25 | 1985-09-25 | Manufacture of compounded ceramics |
Publications (1)
Publication Number | Publication Date |
---|---|
JPS6270041A true JPS6270041A (en) | 1987-03-31 |
Family
ID=16602524
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP21123585A Pending JPS6270041A (en) | 1985-09-25 | 1985-09-25 | Manufacture of compounded ceramics |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS6270041A (en) |
Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH02217246A (en) * | 1989-02-20 | 1990-08-30 | Suzuki Motor Co Ltd | Preparation of inclined functional material |
CN1045946C (en) * | 1991-01-24 | 1999-10-27 | 合肥工业大学 | Ceramic drawing die with precise structure and its production process |
JP2010017565A (en) * | 2009-08-21 | 2010-01-28 | Yoko Oya | Human shape pad for comfortable driving |
CN105459516A (en) * | 2014-08-28 | 2016-04-06 | 比亚迪股份有限公司 | Ceramic substrate and preparation method thereof, and power module |
CN105459515A (en) * | 2014-08-28 | 2016-04-06 | 比亚迪股份有限公司 | Ceramic substrate and preparation method thereof, and power module |
US10710936B2 (en) | 2014-08-28 | 2020-07-14 | Byd Company Limited | Ceramic substrate and its manufacturing method, power module |
-
1985
- 1985-09-25 JP JP21123585A patent/JPS6270041A/en active Pending
Cited By (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH02217246A (en) * | 1989-02-20 | 1990-08-30 | Suzuki Motor Co Ltd | Preparation of inclined functional material |
CN1045946C (en) * | 1991-01-24 | 1999-10-27 | 合肥工业大学 | Ceramic drawing die with precise structure and its production process |
JP2010017565A (en) * | 2009-08-21 | 2010-01-28 | Yoko Oya | Human shape pad for comfortable driving |
CN105459516A (en) * | 2014-08-28 | 2016-04-06 | 比亚迪股份有限公司 | Ceramic substrate and preparation method thereof, and power module |
CN105459515A (en) * | 2014-08-28 | 2016-04-06 | 比亚迪股份有限公司 | Ceramic substrate and preparation method thereof, and power module |
CN105459515B (en) * | 2014-08-28 | 2017-09-29 | 比亚迪股份有限公司 | A kind of ceramic substrate and preparation method thereof and a kind of power model |
US10710936B2 (en) | 2014-08-28 | 2020-07-14 | Byd Company Limited | Ceramic substrate and its manufacturing method, power module |
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