JPS6011265A - Cutting tool ceramics - Google Patents

Cutting tool ceramics

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Publication number
JPS6011265A
JPS6011265A JP58118479A JP11847983A JPS6011265A JP S6011265 A JPS6011265 A JP S6011265A JP 58118479 A JP58118479 A JP 58118479A JP 11847983 A JP11847983 A JP 11847983A JP S6011265 A JPS6011265 A JP S6011265A
Authority
JP
Japan
Prior art keywords
ceramics
weight
powder
cutting
tools
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
Application number
JP58118479A
Other languages
Japanese (ja)
Inventor
裕介 井寄
紀雄 高橋
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Proterial Ltd
Original Assignee
Hitachi Metals Ltd
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Hitachi Metals Ltd filed Critical Hitachi Metals Ltd
Priority to JP58118479A priority Critical patent/JPS6011265A/en
Publication of JPS6011265A publication Critical patent/JPS6011265A/en
Pending legal-status Critical Current

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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】 本発明はセラミック材料に関し、特に切削工具用セラミ
ックスに関するものである。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to ceramic materials, and in particular to ceramics for cutting tools.

切削工具用セラミックスの1つとして良く知られている
アルミナ切削工具は、耐摩耗性に優れている反面・チッ
ピングしやすい短所を有しているため、開発初期より現
在に至るまでセラミックス工具の靭性の改善が開発の大
ぎな目標の1つとされてぎた。これらの要求に対する解
決法の1つとして、A120aに約30重量%のTiC
を複合化し、結晶粒を微細化すると同時に、アルミナ固
有の性質である高温になるほど熱伝導率が低下する欠点
を補い、熱衝撃による耐欠損性を改善したA1゜Oa’
TIC系セラミックス工具が発明された。
Alumina cutting tools, which are well known as one of the ceramics for cutting tools, have excellent wear resistance but are prone to chipping. Improvement has been considered one of the major goals of development. One solution to these requirements is to add approximately 30% by weight TiC to A120a.
A1゜Oa' is a composite of A1゜Oa' that improves fracture resistance due to thermal shock by making the crystal grains finer and compensating for the inherent characteristic of alumina, which is that the thermal conductivity decreases as the temperature increases.
TIC ceramic tools were invented.

Al2O3TfC系セラミックス工具は、耗アルミナに
よるいわゆる白糸セラミックス工具と比較して、高靭性
でしかも熱衝撃による耐欠損性に優れているため、白系
セラミックス工具では使用が困難であった高硬度材料の
旋削加工、鋳鉄材料のフライス加工等の用途に特に威力
を発揮している。しかし、このAl2O3TiC系セラ
ミツクス工具においても、刃先温度が1200℃を越え
る切削条件下では、多量に含まれるTiCの高温硬度が
Al2−03の高温硬度より低下するため、耐摩耗性が
劣り、高硬度材の切削地に境界摩耗が生じ易い欠点があ
った。
Al2O3TfC ceramic tools have higher toughness and better fracture resistance due to thermal shock than so-called white thread ceramic tools made of worn alumina, so they are suitable for turning of high-hardness materials that are difficult to use with white ceramic tools. It is particularly effective in applications such as milling of cast iron materials. However, even in this Al2O3TiC ceramic tool, under cutting conditions where the cutting edge temperature exceeds 1200°C, the high-temperature hardness of the TiC contained in a large amount is lower than that of Al2-03, resulting in poor wear resistance and high hardness. There was a drawback that boundary wear was likely to occur on the cut surface of the material.

本発明は上記従来技術の欠点を改良し、熱伝導度が極め
て高く高靭性で耐チッピング特性の優れた切削工具用セ
ラミックスを提供することを目的とする。
An object of the present invention is to improve the above-mentioned drawbacks of the prior art and to provide ceramics for cutting tools that have extremely high thermal conductivity, high toughness, and excellent chipping resistance.

本発明はAl2O3粉末に5〜20重量%のTiB2粉
末および5〜20重量%のTiN粉末を混合し、さらに
1〜10重量%のZrO2を添加したことを特徴どする
ものである。
The present invention is characterized in that 5-20% by weight of TiB2 powder and 5-20% by weight of TiN powder are mixed with Al2O3 powder, and 1-10% by weight of ZrO2 is further added.

本発明において、Al2O3TiC系セラミックスにお
けるTiCと同様に、Ti B2 、 TiNおよびZ
rO2はAl2O3中に分散した組織になっており、良
く知られているように、アルミナの粒成長を阻止し靭性
を高めるとともに微小なりラックの成長を抑える役割を
果している。
In the present invention, similar to TiC in Al2O3TiC ceramics, TiB2, TiN and Z
rO2 has a structure dispersed in Al2O3, and as is well known, it plays the role of inhibiting grain growth of alumina, increasing toughness, and suppressing the growth of minute racks.

しかしながら、AI 20g Ti N中に、難焼結材
であるTf 82を多」に混合した場合、焼成温度が高
くなり粒径が10μm前後と大きくなる欠点がある。
However, when a large amount of Tf 82, which is a difficult-to-sinter material, is mixed into AI 20g TiN, there is a drawback that the firing temperature becomes high and the particle size increases to around 10 μm.

本発明におけるZr 02の添加はこの欠点を補うもの
で、Al2O37!B2の焼結性を向上させる効果があ
る。また、本発明においては、0.05〜2.5重囲%
のM(10およびAINを添加することにより、さらに
焼結性を向上し粒径の成長を抑えることが出来る。
The addition of Zr 02 in the present invention compensates for this drawback, and Al2O37! This has the effect of improving the sinterability of B2. In addition, in the present invention, 0.05 to 2.5 weight%
By adding M(10) and AIN, sinterability can be further improved and grain size growth can be suppressed.

本発明によるセラミックスは通常、上記組成範囲の混合
粉末を・・熱間加圧することにより得ることができるが
、熱間加圧後さらに熱間静水圧プレスを行なっても、あ
るいは常圧焼成の後熱間静水圧プレスを行なっても同様
の結果を得ることができる。また本発明において、Tl
B2粉末を5〜20重量%に限定した理由は、5以下で
は添加効果がなく、20%以上では粒径が逆に大きく成
長するためである。また、ZrO2に関しては1%未満
で ′はやはり添加効果がなく、10%を越えると耐熱
衝撃性が低下するため1〜10%に限定した。また、M
(10およびAIN粉末の合計量を0.05〜2.5重
量%に限定した理由は、0.05重量%以下ではAl2
011の結晶粒微細化の効果がなく、2.5重量%以上
になると結晶粒界にスピネル層が生じ、脆化するためで
ある。
Ceramics according to the present invention can usually be obtained by hot pressing a mixed powder having the above composition range, but it can also be obtained by hot isostatic pressing after hot pressing, or after normal pressure firing. Similar results can be obtained by hot isostatic pressing. Further, in the present invention, Tl
The reason why the amount of B2 powder is limited to 5 to 20% by weight is that if it is less than 5%, there is no effect of adding it, and if it is more than 20%, the particle size will conversely grow large. Regarding ZrO2, if it is less than 1%, there is no effect when added, and if it exceeds 10%, the thermal shock resistance decreases, so the content was limited to 1 to 10%. Also, M
(The reason why the total amount of 10 and AIN powder was limited to 0.05 to 2.5% by weight is that below 0.05% by weight, Al2
This is because there is no grain refining effect of 011, and when the amount exceeds 2.5% by weight, a spinel layer is formed at the grain boundaries, resulting in embrittlement.

また、Y203の添加量をZrO2に対しモル比で1.
0〜3.0モル%に限定したのは、Zr 02の結晶型
を正方晶(を相)主体とし破壊強度を向上させるためで
、1.0%未満では単斜晶(M相)が主体となり、3.
0%を越えると立方晶(C相)が主体となり共にY 2
0 a添加の効果がうすい。
In addition, the amount of Y203 added was 1.0 molar ratio to ZrO2.
The reason for limiting it to 0 to 3.0 mol% is to make Zr 02's crystal type mainly tetragonal (phase) to improve fracture strength, and when it is less than 1.0%, it is mainly monoclinic (M phase). So, 3.
When it exceeds 0%, the cubic crystal (C phase) becomes the main component and both Y2
0 The effect of adding a is weak.

実施例1 平均粒径1.2μmのTi 82粉末を15重量%。Example 1 15% by weight of Ti 82 powder with an average particle size of 1.2 μm.

平均粒径0.7μmのTiN粉末を10重量%、平均粒
径0.1μmのZrO2粉末を5重量%、平均粒径0.
1μmのAl2O3粉末を残部とし、さらにMa O0
,5重量%、AlN1.0重量%配合し、エチルアルコ
ールを使用してアルミナ製のボールミルで48時間混合
粉砕したのち真空中で乾燥したのち、2t/cm2で成
形し、真空中1500℃で圧力200kg/cII12
をかけながら10分間保持する加圧焼結を行ない焼結体
を得た。
10% by weight of TiN powder with an average particle size of 0.7 μm, 5% by weight of ZrO2 powder with an average particle size of 0.1 μm, and 0.5% by weight of ZrO2 powder with an average particle size of 0.1 μm.
The remainder is 1 μm Al2O3 powder, and further MaO0
, 5% by weight, and 1.0% by weight of AlN were mixed and ground in an alumina ball mill using ethyl alcohol for 48 hours, dried in vacuum, molded at 2t/cm2, and pressed at 1500°C in vacuum. 200kg/cII12
Pressure sintering was carried out by holding for 10 minutes while applying pressure to obtain a sintered body.

本焼結体より切削工具用チップ5NGN453を作製し
、従来より広範に使用されているAl2Q3−30%T
iCチップを比較材として用い、被削材DAC(H86
5)を用いて切削テストを行なった。
Cutting tool tip 5NGN453 was made from this sintered body, and Al2Q3-30%T, which has been widely used in the past, was made from this sintered body.
Using the iC chip as a comparison material, the workpiece material DAC (H86
A cutting test was conducted using 5).

切削速度は50 m/minおよび70 m/n+in
切り込みは各1.5a+n+、送りは0.4m1ll/
 reVとした。
Cutting speed is 50 m/min and 70 m/n+in
The depth of cut is 1.5a+n+ each, and the feed is 0.4ml/ll/
It was set as reV.

第1図に示す如く、本発明によるセラミックスはいずれ
の場合も従来のAl2O37IC系セラミツクスに比べ
て極めて境界摩耗損が少なく、良好な切削性能を示した
As shown in FIG. 1, the ceramics according to the present invention exhibited excellent cutting performance with significantly less boundary wear loss than the conventional Al2O37IC ceramics.

実施例2 Tf B2粉末を10重四%、 Ti N粉末を10重
量%、ZrO2粉末を5重量%、Y20a粉末を0.1
2重r%、残部Al2O3粉末を配合し、エチルアルコ
ールを使用してアルミナ製のボールミルで48時間混合
粉砕したのち真空中で乾燥したのち、2 t /cm’
で成形し、真空中1500℃、圧力200kg/’ca
n’で加圧焼結を行ない焼結体を得た。
Example 2 10% by weight of TfB2 powder, 10% by weight of TiN powder, 5% by weight of ZrO2 powder, 0.1% of Y20a powder
2% by weight, the balance being Al2O3 powder, mixed and pulverized for 48 hours in an alumina ball mill using ethyl alcohol, dried in vacuum, and then 2 t/cm'
molded in vacuum at 1500℃ and pressure 200kg/'ca.
Pressure sintering was performed at n' to obtain a sintered body.

本焼結体から8X 4X 25+11111の試験片を
切出し抗折試験を実施した。平均抗折強度は140kg
 /mm2で、市販のAI 203−30%TiCセラ
ミックスと比較して極めて高い強度を有することが証明
された。
A test piece of 8×4×25+11111 was cut out from this sintered body and subjected to a bending test. Average bending strength is 140kg
/mm2, which proved to have extremely high strength compared to commercially available AI 203-30% TiC ceramics.

次に、本焼結体より切削工具用チップ5NGN432を
作製し、市販(7)AI 203 30%Tf Cチッ
プを比較材として用い、被削材SCM440を用いてフ
ライス切削テストを行なった。切り込みは2n+mどし
た。
Next, a cutting tool tip 5NGN432 was prepared from this sintered body, and a milling test was conducted using a commercially available (7) AI 203 30% Tf C tip as a comparison material and a workpiece material SCM440. The incision was 2n+m.

第2図に示す如く、本発明によるセラミックスは従来の
Al2O3TiC系セラミックスに比べて広範な切削領
域を示した。
As shown in FIG. 2, the ceramic according to the present invention exhibited a wider cutting area than the conventional Al2O3TiC ceramic.

上記実施例から明らかな如く、本発明による切削工具用
セラミックスは境界摩耗門が少なく、かつ高靭性であり
、いわゆる熱系工具用セラミックスとして優れた特性を
示し、工業上極めて有用なものである。
As is clear from the above examples, the ceramics for cutting tools according to the present invention have fewer boundary wear gates and are highly tough, exhibiting excellent properties as so-called ceramics for thermal tools, and are extremely useful industrially.

【図面の簡単な説明】[Brief explanation of the drawing]

第1図は本発明によるセラミックスおよび従来のAI 
20.−Ti C系セラミックスによる切削テスト結果
を示す特性曲線、第2図は同じく本発明によるセラミッ
クスおよび従来のAl2O3〜TiCセラミツクスによ
るフライス加工テスト結果を示すものである。 送り 2 図 送り
Figure 1 shows ceramics according to the present invention and conventional AI
20. -Characteristic curves showing cutting test results for TiC ceramics; FIG. 2 also shows milling test results for ceramics according to the present invention and conventional Al2O3 - TiC ceramics. Feed 2 Figure feed

Claims (1)

【特許請求の範囲】 1、重量化で5〜20%TiB2.5〜20%Ti N
。 1〜10%Zr 02 、残部′tJ<A1゜03およ
び不可避不純物であることを特徴とする切611工具用
セラミックス。 2、特許請求の範囲第1項8己載のものにお(1て、A
I N、MU 0(7)一方又’ri 双方ヲ合it 
0.05〜2.5重量%添加したことを特徴とする切肖
11工具用セラミックス。 3、特許請求の範囲第1項8己載のものにおし1て、Z
rO2に対して1.0〜3.0%モル比のY 20 a
を含有することを特徴とする切m I具用セラミックス
。 4、特許請求の範囲第2項記載のものにお(1て、Zr
O2に対して 1.0〜3.0%モル比のY 203を
含有することを特徴とする切I!111工具用セラミッ
クス。
[Claims] 1. 5-20% TiB by weight 2.5-20% TiN
. A ceramic for a cutting 611 tool, characterized in that it contains 1 to 10% Zr 02 , the remainder 'tJ<A1°03 and unavoidable impurities. 2. Claims 1, 8.
I N, MU 0 (7) On the other hand, also 'ri, both together.
Ceramics for cut 11 tools, characterized in that 0.05 to 2.5% by weight is added. 3.Claim 1, paragraph 8.
1.0-3.0% molar ratio of Y20a to rO2
Ceramics for cutting tools, characterized by containing. 4. What is described in claim 2 (1) Zr
Cut I! characterized by containing Y203 in a molar ratio of 1.0 to 3.0% with respect to O2! 111 Ceramics for tools.
JP58118479A 1983-06-30 1983-06-30 Cutting tool ceramics Pending JPS6011265A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP58118479A JPS6011265A (en) 1983-06-30 1983-06-30 Cutting tool ceramics

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP58118479A JPS6011265A (en) 1983-06-30 1983-06-30 Cutting tool ceramics

Publications (1)

Publication Number Publication Date
JPS6011265A true JPS6011265A (en) 1985-01-21

Family

ID=14737688

Family Applications (1)

Application Number Title Priority Date Filing Date
JP58118479A Pending JPS6011265A (en) 1983-06-30 1983-06-30 Cutting tool ceramics

Country Status (1)

Country Link
JP (1) JPS6011265A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS6241776A (en) * 1985-08-15 1987-02-23 日本特殊陶業株式会社 Fiber reinforced composite material for tool
WO2023120468A1 (en) * 2021-12-21 2023-06-29 東ソー株式会社 Ceramic matrix composite material and method for manufacturing same

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS6241776A (en) * 1985-08-15 1987-02-23 日本特殊陶業株式会社 Fiber reinforced composite material for tool
JPH0520382B2 (en) * 1985-08-15 1993-03-19 Ngk Spark Plug Co
WO2023120468A1 (en) * 2021-12-21 2023-06-29 東ソー株式会社 Ceramic matrix composite material and method for manufacturing same

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