JPS59102863A - Ceramic sintering body composition - Google Patents
Ceramic sintering body compositionInfo
- Publication number
- JPS59102863A JPS59102863A JP57210940A JP21094082A JPS59102863A JP S59102863 A JPS59102863 A JP S59102863A JP 57210940 A JP57210940 A JP 57210940A JP 21094082 A JP21094082 A JP 21094082A JP S59102863 A JPS59102863 A JP S59102863A
- Authority
- JP
- Japan
- Prior art keywords
- body composition
- sintered body
- oxides
- ceramic sintering
- sintering body
- 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.)
- Granted
Links
Landscapes
- Compositions Of Oxide Ceramics (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】
不発1y′Jは切削ハイトチツブ、軸受等高い硬度、耐
1r耗性を要求する各種物品に使用するセラミック焼結
体に関するものである。DETAILED DESCRIPTION OF THE INVENTION The non-explosion 1y'J relates to ceramic sintered bodies used in various articles requiring high hardness and 1R wear resistance, such as cutting height chips and bearings.
従来より、A1□0.又はMg 0等微量の粒成長抑制
剤を3むA1□03 焼結体は硬度、耐摩耗性がill
<各種の耐摩耗磁器として、特に切削用ハイドチップ
として高速切削やht ’M仕上げに広く利用されてい
るが、靭性に乏しいため使用領域が軽切削のみに限定さ
れている。このような欠点を除くためにTj Cを添加
した高靭性セラミックスが開発され、セラミックス具の
切削域を広めた。しかし、汎用材質として用いられるに
至ってはおらず、機械的振動、衝撃を伴う重切削には、
限られた領域のみ用いられているにすぎない。Conventionally, A1□0. Or the A1□03 sintered body containing a trace amount of grain growth inhibitor such as Mg 0 has illumination hardness and wear resistance.
<It is widely used as a variety of wear-resistant porcelain, especially as a cutting hide tip for high-speed cutting and ht'M finishing, but its use is limited to light cutting only due to its poor toughness. In order to eliminate these drawbacks, high-toughness ceramics added with Tj C were developed, and the cutting range of ceramic tools was expanded. However, it has not yet been used as a general-purpose material, and is not suitable for heavy cutting that involves mechanical vibration and impact.
It is only used in a limited area.
本発明は、このAl2O3Ti C系セラミック焼結体
におけるTi C強化を目的とし、重量基準でTiCl
3〜40%に第1添加物として、Nb、V。The purpose of the present invention is to strengthen TiC in this Al2O3TiC ceramic sintered body, and to strengthen TiC on a weight basis.
Nb, V as the first additive in 3-40%.
Ta、Zr及びHfのうち一種以上の金属又は酸化物1
〜10%、第2添加物としてCaO,Mg O。One or more metals or oxides of Ta, Zr and Hf 1
~10%, CaO, MgO as second additive.
Y 203 IS iOユ+ N iO+ DV 20
3及び希土類元素の酸化物のうち一種以上0.05〜3
.0%残部A 120.から成ることを特徴とするセラ
ミック焼結体組成物を提供するものである。Y 203 IS iO+ N iO+ DV 20
3 and one or more oxides of rare earth elements 0.05 to 3
.. 0% balance A 120. The present invention provides a ceramic sintered body composition characterized by comprising:
第1添加物としてNb、V、Zr、Ta及びHfのうち
一種以上の金属又は酸化物を添加する理由は、Ti C
が微細で均一に分散した組織を得ることができ、またこ
の結果、硬度が増し、耐摩耗性も向上して工具としての
性能を向上せしめるためである。この場合Nb、V、Z
r、Ta及びHfは金属添加のみならず、金属酸化物又
は有機化合物の形で添加してもよく、要するに焼結中、
金属又は酸化物に変化する上記の物質ならば同様の効果
が得られる。この場合、金属は1部又は大半が酸化物に
変化する。そしてこの効果は1%以下では効果が不十分
であり、10%を超えると却って靭性か乏しくなる。The reason for adding one or more metals or oxides among Nb, V, Zr, Ta, and Hf as the first additive is that TiC
This is because a fine and uniformly dispersed structure can be obtained, and as a result, hardness is increased and wear resistance is also improved, thereby improving performance as a tool. In this case Nb, V, Z
r, Ta and Hf are not only added as metals, but may also be added in the form of metal oxides or organic compounds; in short, during sintering,
Similar effects can be obtained if the above-mentioned substances change into metals or oxides. In this case, part or most of the metal is converted into an oxide. This effect is insufficient if it is less than 1%, and if it exceeds 10%, the toughness becomes poor.
又、第2添加物としてCa + M g + Y 、’
S i+ Z r +Ni 、Dy及び希土類元素の
酸化物のうち1種以上を添加する理由は、これらがアル
ミナ結晶粒子の成長を抑制し、同時に焼結を促進するた
めである。その効果は0.05%以下では効果が乏しく
3.0%を超えると高温又は室温の耐摩耗性、靭性が低
下する。Also, as a second additive Ca + M g + Y,'
The reason why one or more of S i + Z r +Ni, Dy, and an oxide of a rare earth element is added is that these suppress the growth of alumina crystal particles and promote sintering at the same time. If the content is less than 0.05%, the effect is poor, and if it exceeds 3.0%, the wear resistance and toughness at high temperature or room temperature decrease.
次にその製造法を述べると、周知の窯業組成物の製造法
が利用できるが、焼成雰囲気は特に非酸化性であること
が必要で、酸素を多く含む雰囲気・
中では、TiCが酸化し本来の特性を発揮しない。Next, regarding its production method, well-known production methods for ceramic compositions can be used, but the firing atmosphere must be particularly non-oxidizing.In an atmosphere containing a lot of oxygen, TiC will oxidize and does not exhibit its characteristics.
以下実施例により一層具体的に説明するが、本発明は実
施例の範囲に限定されるものではない。The present invention will be explained in more detail with reference to Examples below, but the present invention is not limited to the scope of the Examples.
実施例1
粒径1μm以下が70%のα−A1209.平均粒径1
.2.um全炭素量19.4%のTi C及び325メ
7シユを通過させた添加物を第1表に示す割合で配合し
、ステンレスボールミル中でアセトンと共に約30時間
湿式粉砕し、そのアセトンを乾燥機で揮散し、乳鉢で6
0メソシユ篩を全量通過するまで微粉砕して素地粉末(
A)(以下(A)と略称する)を調製する。(A)にパ
ラフィン5%を添加し、60メツシユ篩を全量通過させ
た後、圧力1 t / Cm′L で16X16X7.
5mmの直方体に加圧成形する。得られた成形体(B)
(以下(B)と略称する)を、減圧アルゴン雰囲気下第
2表に示す焼結温度で、1時間焼結(以下「普通焼結」
と称する)させる。得られた焼結体をダイヤモンド砥石
によっ一寸法5NGN432TN、表面3S以下に研磨
し、緒特性を測定した結果を第2表に示す。Example 1 α-A1209 with 70% particle size of 1 μm or less. Average particle size 1
.. 2. TiC with a total carbon content of 19.4% and additives passed through a 325 mesh were mixed in the proportions shown in Table 1, wet milled with acetone for about 30 hours in a stainless steel ball mill, and the acetone was dried. Volatilize with a machine and 6 in a mortar.
Finely grind the base powder (
A) (hereinafter abbreviated as (A)) is prepared. After adding 5% paraffin to (A) and passing the entire amount through a 60-mesh sieve, it was sieved at a pressure of 1 t/Cm'L to 16X16X7.
Pressure mold into a 5 mm rectangular parallelepiped. Obtained molded body (B)
(hereinafter referred to as (B)) was sintered for 1 hour at the sintering temperature shown in Table 2 under a reduced pressure argon atmosphere (hereinafter referred to as "normal sintering").
). The obtained sintered body was polished with a diamond grindstone to a dimension of 5NGN432TN and a surface of 3S or less, and its properties were measured. The results are shown in Table 2.
実施例2
実施例1と同様に調製して得られた(A)を第2表に示
す焼結温度で、圧力200 kg/crA、加圧焼成時
間15分の条件下で、加圧焼結法により黒鉛型内におい
て13X13X6mmの角板に焼結させる。実施例1と
同様にvr磨し、緒特性を測定した結果を第2表に示す
。Example 2 (A) prepared in the same manner as in Example 1 was subjected to pressure sintering at the sintering temperature shown in Table 2, under the conditions of a pressure of 200 kg/crA and a pressure firing time of 15 minutes. 13 x 13 x 6 mm square plates are sintered in a graphite mold by the method. It was subjected to VR polishing in the same manner as in Example 1, and its properties were measured. The results are shown in Table 2.
実施例3
実施例工と同様に成形した(B)を減圧アルゴン雰囲気
下第2表に示す一次焼結温度、1時間の条件で一次焼結
体を作成し、これを第2表に示す焼結温度、圧力150
0kg/CIIT、保持時間1時間の条件で等方加圧焼
結法により焼結させる。実施例1と同様にvr磨し、緒
特性を測定した結果を第2表に示す。Example 3 A primary sintered body was prepared from (B), which was molded in the same manner as in Example 1, under a reduced pressure argon atmosphere at the primary sintering temperature shown in Table 2 for 1 hour. Freezing temperature, pressure 150
Sintering is performed by isostatic pressure sintering under the conditions of 0 kg/CIIT and a holding time of 1 hour. It was subjected to VR polishing in the same manner as in Example 1, and its properties were measured. The results are shown in Table 2.
第2表に示すように本発明のセラミック焼結体はAl2
O3単独、A Iz 03− T i C系あるいは本
発明に規定する各組成物の配合量から外れたセラミック
焼結体に比し、硬度及び切削性能を著しく改善し、機械
的振動や衝撃を伴う重切削を可能とすることを確かやた
。As shown in Table 2, the ceramic sintered body of the present invention has Al2
Compared to O3 alone, A Iz 03-T i C system, or a ceramic sintered body that does not meet the blending amount of each composition specified in the present invention, the hardness and cutting performance are significantly improved, and the material is less susceptible to mechanical vibration and impact. It was confirmed that heavy cutting is possible.
本発明組成により得られたセラミ・ツク焼結体は鋳物、
高硬度材、高二・ノケル合金以外の金属例えばアルミニ
ウム、スチール等や非金属の切削工具として使用でき、
更には振動が激しくかかるあるいは高熱のかかる機械部
品にも使用することができる。The ceramic sintered body obtained by the composition of the present invention is a casting,
It can be used as a cutting tool for high hardness materials, metals other than high-density and Nokel alloys, such as aluminum, steel, etc., and non-metals.
Furthermore, it can be used for mechanical parts that are subject to intense vibration or high heat.
Claims (1)
b、 V、 Ta、 Zr、及びHfのうち一種以上の
金属又は酸化物1〜10%、第2添加物としてCa O
,ム4go、Yz03 、 SI Oz 、 Zr
Oz lNi O,Dy2O3、及び希土類元素の酸
化物のうら一種以上0.05〜3.0%残部A1□o3
がら成る耐摩耗性及び靭性のすくれたセラミック焼
結体組成物。Based on city fa standards, N is added as the first additive to TiCl3-40%.
b, 1 to 10% of one or more metals or oxides among V, Ta, Zr, and Hf, CaO as a second additive
, Mu4go, Yz03, SI Oz, Zr
Oz lNi O, Dy2O3, and one or more oxides of rare earth elements 0.05-3.0% balance A1□o3
A ceramic sintered body composition with excellent wear resistance and toughness.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP57210940A JPS59102863A (en) | 1982-12-01 | 1982-12-01 | Ceramic sintering body composition |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP57210940A JPS59102863A (en) | 1982-12-01 | 1982-12-01 | Ceramic sintering body composition |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS59102863A true JPS59102863A (en) | 1984-06-14 |
JPS6335587B2 JPS6335587B2 (en) | 1988-07-15 |
Family
ID=16597604
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP57210940A Granted JPS59102863A (en) | 1982-12-01 | 1982-12-01 | Ceramic sintering body composition |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS59102863A (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5196385A (en) * | 1985-08-06 | 1993-03-23 | Ngk Spark Plug Co., Ltd. | Process for the preparation of a heat-resistant and wear resistant ceramic material |
US20180170811A1 (en) * | 2015-06-17 | 2018-06-21 | National Institute For Materials Science | Oxidation-induced self-healing ceramic composition containing healing activator, method for producing same, use of same, and method for enhancing functionality of oxidation-induced self-healing ceramic composition |
Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5391922A (en) * | 1977-08-12 | 1978-08-12 | Nippon Tungsten | Method of making material for ceramic tools |
JPS5738369A (en) * | 1980-08-21 | 1982-03-03 | Mitsubishi Metal Corp | High strength and high hardness alumina ceramic |
-
1982
- 1982-12-01 JP JP57210940A patent/JPS59102863A/en active Granted
Patent Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5391922A (en) * | 1977-08-12 | 1978-08-12 | Nippon Tungsten | Method of making material for ceramic tools |
JPS5738369A (en) * | 1980-08-21 | 1982-03-03 | Mitsubishi Metal Corp | High strength and high hardness alumina ceramic |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5196385A (en) * | 1985-08-06 | 1993-03-23 | Ngk Spark Plug Co., Ltd. | Process for the preparation of a heat-resistant and wear resistant ceramic material |
US20180170811A1 (en) * | 2015-06-17 | 2018-06-21 | National Institute For Materials Science | Oxidation-induced self-healing ceramic composition containing healing activator, method for producing same, use of same, and method for enhancing functionality of oxidation-induced self-healing ceramic composition |
US10822277B2 (en) * | 2015-06-17 | 2020-11-03 | National Institute For Materials Science | Oxidation-induced self-healing ceramic composition containing healing activator, method for producing same, use of same, and method for enhancing functionality of oxidation-induced self-healing ceramic compositions |
Also Published As
Publication number | Publication date |
---|---|
JPS6335587B2 (en) | 1988-07-15 |
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