JPH05319935A - Sintered tib2 ceramic - Google Patents

Sintered tib2 ceramic

Info

Publication number
JPH05319935A
JPH05319935A JP3282730A JP28273091A JPH05319935A JP H05319935 A JPH05319935 A JP H05319935A JP 3282730 A JP3282730 A JP 3282730A JP 28273091 A JP28273091 A JP 28273091A JP H05319935 A JPH05319935 A JP H05319935A
Authority
JP
Japan
Prior art keywords
binder
tib2
tib
tin
sintered 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.)
Withdrawn
Application number
JP3282730A
Other languages
Japanese (ja)
Inventor
Hideo Tsunoda
英雄 角田
Yorimasa Takeda
頼正 竹田
Tsuneo Egawa
庸夫 江川
Tetsuo Ichikizaki
哲雄 市来崎
Jun Takashina
純 高階
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.)
Mitsubishi Heavy Industries Ltd
Original Assignee
Mitsubishi Heavy Industries 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 Mitsubishi Heavy Industries Ltd filed Critical Mitsubishi Heavy Industries Ltd
Priority to JP3282730A priority Critical patent/JPH05319935A/en
Publication of JPH05319935A publication Critical patent/JPH05319935A/en
Withdrawn legal-status Critical Current

Links

Abstract

PURPOSE:To obtain a sintered TiB2 ceramic having improved chipping resistance and cutting performance by mixing TiB2 with TiN or a binder consisting of TiN partly substituted with AIN, SiC, TiB2 or ZrO2 at a prescribed mixing ratio and sintering the powdery mixture. CONSTITUTION:The sintered TiB2 ceramic material is formed by sintering a powdery mixture of 30-70vol.% of TiB2 powder and a binder. The binder is composed mainly of TiN and a part of the binder may be replaced with one or more components selected from AlN, SiC, TiB2 and ZrO2. The sintered ceramic material is resistant to chipping caused by breakage of the part or falling-off of crystal particle and has excellent chipping resistance and cutting performance.

Description

【発明の詳細な説明】Detailed Description of the Invention

【0001】[0001]

【産業上の利用分野】本発明は、TiB2 セラミックス
焼結体に関し、特に例えば軸受鋼等の高硬度材料の高速
切削加工に用いて最適なものである。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a TiB 2 ceramics sintered body, and is most suitable for high speed cutting of a high hardness material such as bearing steel.

【0002】[0002]

【従来の技術】従来において、被削材の硬度がロック・
ウェル硬さ(HRC)で、60以上の高硬度材料の加工
は、切削加工が困難であるため、主としてダイヤモンド
砥粒等による研削加工を行っている。しかしながら該研
削加工は、加工速度が遅いため、工程短縮が思うように
ならない。
2. Description of the Related Art Conventionally, the hardness of the work material is locked.
Since it is difficult to cut a high hardness material having a well hardness (H RC ) of 60 or more, a grinding process is mainly performed by using diamond abrasive grains or the like. However, since the grinding process has a low processing speed, the process cannot be shortened.

【0003】この問題を解決するため、高硬度材料を切
削加工する工具として、WC−Coを主成分とする超
硬合金工具、TiC−TiNと−Ni−Mo系のサー
メット工具、Al2 3 を主成分とするセラミックス
工具、CBN粒子を高温高圧で焼結したCBN焼結工
具が種々開発されており、新しい機械加工の分野が展開
されつつある。そしてこの高硬度材料の切削加工用工具
としては、(イ)工具摩耗量が小さいこと、(ロ)切削
された被削材料の加工面粗さが良好なこと、等の性能が
必要とされている。
[0003] To solve this problem, a tool for cutting a high-hardness material, cemented carbide tools mainly composed of WC-Co, TiC-TiN and -Ni-Mo cermet tool, Al 2 O 3 Various ceramic tools containing C as a main component and CBN sintering tools obtained by sintering CBN particles at high temperature and high pressure have been developed, and a new field of machining is being developed. And as a cutting tool for this high hardness material, performance such as (a) small amount of tool wear, (b) good cut surface roughness of the cut work material, etc. is required. There is.

【0004】[0004]

【発明が解決しようとする課題】しかしながら上述した
高硬度材料用工具のうち、超硬合金工具やサーメット工
具は金属バインダが加工時の発熱により塑性変形を起こ
し、摩耗が短時間に進行するため適用できないという問
題がある。また、セラミックス工具は、超硬合金やサー
メットと比較して欠損しやすいこと、及びピッチング
(微小領域での剥離亀裂現象をいう)を起こしやすいこ
とから、加工面の粗さが悪く、適用できないという問題
がある。更に、CBN焼結工具は高硬度材料の切削加工
用の要求性能には合致しているものの、CBNを焼結す
るために1600℃以上の高温及び5万気圧以上の高圧
が必要であると共に製造設備が特殊なもので高価とな
り、該CBN焼結工具の製造は非常に高価になるという
問題がある。
However, among the above-mentioned tools for high hardness materials, cemented carbide tools and cermet tools are applied because the metal binder causes plastic deformation due to heat generated during processing and wear progresses in a short time. There is a problem that you can not. In addition, ceramic tools are more likely to be chipped than cemented carbide or cermet, and are more likely to cause pitting (which is a phenomenon of peeling cracks in a minute area), so that the roughness of the machined surface is poor and it cannot be applied. There's a problem. Further, although the CBN sintering tool meets the required performance for cutting hard materials, it requires a high temperature of 1600 ° C or higher and a high pressure of 50,000 atmospheres or more to sinter CBN. There is a problem that the equipment is special and expensive, and the manufacturing of the CBN sintering tool is very expensive.

【0005】本発明はこのような事情に鑑み、高硬度材
料の高速切削加工に用いて最適なTiB2 セラミックス
焼結体を提供することを目的とする。
In view of such circumstances, it is an object of the present invention to provide an optimal TiB 2 ceramics sintered body which is used for high speed cutting of a high hardness material.

【0006】[0006]

【課題を解決するための手段】前記目的を達成する本発
明に係るTiB2 セラミックス焼結体は、30〜70体
積%のTiB2 と、バインダの主成分としてのTiNと
混合粉末を焼結してなることを特徴とし、また、上記T
iB2 セラミックス焼結体バインダの一部をAlN,S
iC,Al2 3 及びZrO2 より選ばれた一種以上で
置換したことを特徴とする。
A TiB 2 ceramics sintered body according to the present invention, which achieves the above object, is obtained by sintering 30 to 70% by volume of TiB 2 and TiN as a main component of a binder and a mixed powder. In addition, the above T
Part of the iB 2 ceramics sintered body binder is AlN, S
It is characterized in that it is substituted with one or more selected from iC, Al 2 O 3 and ZrO 2 .

【0007】以下、本発明の内容を説明する。本発明T
iB2 セラミックス焼結体の模式断面図を図1に示す。
TiB2 セラミックス焼結体11は主成分のTiB2
子12と、バインダ13とで構成されてなるものであ
る。本発明に係るTiB2 セラミックス焼結体は、Ti
2 粒子12を30〜70体積%用いる。本発明でTi
2 を主成分とするのは、CBNやダイヤモンドに次ぐ
硬さを備えており、優れた耐摩耗性を示すためである。
またCBN等と異なり、特殊な圧力を必要とせず焼結で
き作業性が向上する。ここでTiB2 粒子12を30〜
70体積%とするのは、30体積%未満では、硬さが低
下し欠損しやすくなり、一方、70体積%を超えても、
TiB2 粒子の脱落をバインダが防止できず、被削材の
表面粗さを低下させるため、共に好ましくないからであ
る。また、図1に示したように本発明では、骨格層とし
てTiB2 粒子12を用いており、従って、サブミクロ
ン単位のものより、0.5μm以上、5μm以下程度の原
料が望ましい。これは微細な粒子を用いると、バインダ
部に混入しバインダの接着特性を大きく低下させ好まし
くないからである。
The contents of the present invention will be described below. Invention T
A schematic sectional view of the iB 2 ceramics sintered body is shown in FIG.
The TiB 2 ceramics sintered body 11 is composed of TiB 2 particles 12 as a main component and a binder 13. The TiB 2 ceramics sintered body according to the present invention is made of Ti
30 to 70% by volume of B 2 particles 12 are used. In the present invention Ti
The main component of B 2 is that it has hardness second only to CBN and diamond and exhibits excellent wear resistance.
Further, unlike CBN or the like, it can be sintered without requiring a special pressure and workability is improved. Here, the TiB 2 particles 12 are
When the content is 70% by volume, when the content is less than 30% by volume, the hardness is lowered and the chip tends to be lost.
This is because the binder cannot prevent the TiB 2 particles from coming off and the surface roughness of the work material is reduced, which is not preferable. Further, as shown in FIG. 1, in the present invention, the TiB 2 particles 12 are used as the skeleton layer. Therefore, it is preferable to use a raw material having a size of 0.5 μm or more and 5 μm or less rather than a submicron unit. This is because the use of fine particles is not preferable because it mixes in the binder portion and the adhesive property of the binder is greatly deteriorated.

【0008】バインダ13は、TiNを主成分とする。
TiNとセラミックスのなかでは特殊な室温でも塑性変
形する金属的な性質を持っている。また、TiB2 粒子
12との接合性も高いため、これ等により、焼結体を強
固で粘り強いものにする効果がある。但し、硬さが、他
のセラミックス材と比較して小さいため、これを改善す
るため、高硬度材加工等、高硬度が必要な場合にはその
一部をAlN,SiC,Al2 3 及びZrO2 等で置
換する。これらの置換材は、焼結体中でSialon化合物を
形成し高強度の焼結体にする。また、この反応により、
SiCのCが遊離するため、このCがTiNの硬さを上
げる効果が見られる。
The binder 13 has TiN as a main component.
Among TiN and ceramics, it has a metallic property of being plastically deformed even at a special room temperature. Further, since it has a high bondability with the TiB 2 particles 12, these have an effect of making the sintered body strong and tenacious. However, since the hardness is smaller than that of other ceramic materials, in order to improve this, when high hardness is required such as in processing of high hardness material, a part of AlN, SiC, Al 2 O 3 and Substitute with ZrO 2 . These substitution materials form a Sialon compound in the sintered body to make a high-strength sintered body. Also, due to this reaction,
Since C of SiC is released, this C has an effect of increasing the hardness of TiN.

【0009】以上のように構成された焼結体は、特に、
従来のセラミックス工具の課題であった高硬度被削材の
断続切削加工時の耐欠損性を著しく高める作用がある。
The sintered body constructed as above is
It has the effect of significantly increasing the fracture resistance during interrupted cutting of high hardness work materials, which has been a problem of conventional ceramics tools.

【0010】[0010]

【実施例】以下、本発明の好適な一実施例について詳細
に説明する。
DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS A preferred embodiment of the present invention will be described in detail below.

【0011】(焼結体の製造方法例)TiB2 粒子は、
平均径が1μmの市販の研磨材用を用いた。TiN,A
lN,SiC,Al2 3 ,ZrN2 のバインダ成分
は、気相合成法や、共沈法等、製法は異なるが、いずれ
も一次粒子の平均径が、0.5μm以下のサブミクロン粒
子を用いた。これらを原料として用い、下記「表1」に
記載の組成に配合し、更にエタノールを加えて湿式混合
し、次いで乾燥して原料粉を得た。この原料粉を所定の
温度で真空中でホットプレス(圧力400kgf /cm2
し、焼結した。その後、スローアウェイチップ(ISO
記号SNMN432(加工後寸法12.7mm×12.7mm×4.
76mm、コーナ半径0.8mm))の形状に加工して工具と
した。
(Example of method for producing sintered body) TiB 2 particles are
A commercially available abrasive having an average diameter of 1 μm was used. TiN, A
The binder components of 1N, SiC, Al 2 O 3 and ZrN 2 are different in the production method such as the vapor phase synthesis method and the coprecipitation method, but the average diameter of the primary particles is submicron particles of 0.5 μm or less. Using. Using these as raw materials, they were blended to the composition shown in the following "Table 1", ethanol was further added and wet mixed, and then dried to obtain raw material powder. This raw material powder is hot pressed in a vacuum at a predetermined temperature (pressure 400 kgf / cm 2 ).
And sintered. After that, throw away tip (ISO
Symbol SNMN432 (Dimensions after processing 12.7 mm x 12.7 mm x 4.
76 mm, corner radius 0.8 mm)) and processed into a tool.

【0012】得られた工具を用い、以下の条件で切削試
験を行ない、それぞれの評価を行った。 ・被削材:SUJ2(HRC62程度) ・切削速度:100m/min ・切り込み:0.1mm/rev ・送り:0.1mm/rev ・断続性能:欠損までの断続回数 この切削試験結果を表1に示す。尚、ここで比較材とし
たCBN焼結工具は、他社市販品である。
Using the obtained tools, a cutting test was carried out under the following conditions to evaluate each of them. -Work material: SUJ2 (H RC 62 or so) -Cutting speed: 100 m / min-Cutting depth: 0.1 mm / rev-Feeding: 0.1 mm / rev-Intermittent performance: Intermittent frequency until breakage This cutting test result is shown. Shown in 1. The CBN sintering tool used as a comparative material here is a commercial product of another company.

【0013】[0013]

【表1】 [Table 1]

【0014】表1の結果より、本発明焼結体は、従来の
セラミックス工具と比較して、優れた耐欠損性を備えて
おり、高価なCBN焼結工具並の切削性能を持つことが
わかる。
From the results shown in Table 1, it can be seen that the sintered body of the present invention has excellent fracture resistance as compared with the conventional ceramics tool and has cutting performance comparable to that of an expensive CBN sintered tool. ..

【0015】[0015]

【発明の効果】以上実施例と共に説明したように本発明
によれば、欠損や結晶粒の脱落によるチッピングが防止
されたTiB2 セラミックス焼結体を提供でき、例えば
特に軸受鋼等の高硬度材の切削加工等に使用した場合、
優れた性能を発揮できるという効果を奏する。
According to the present invention, as described above with reference to the embodiments, it is possible to provide a TiB 2 ceramics sintered body in which chipping due to defects and drop of crystal grains is prevented. For example, particularly high hardness materials such as bearing steels can be provided. When used for cutting, etc.,
It has the effect of exhibiting excellent performance.

【図面の簡単な説明】[Brief description of drawings]

【図1】TiB2 セラミックス焼結体の拡大断面模式図
である。
FIG. 1 is an enlarged schematic sectional view of a TiB 2 ceramics sintered body.

【符号の説明】[Explanation of symbols]

11 TiB2 セラミックス焼結体 12 TiB2 粒子 13 バインダ11 TiB 2 ceramics sintered body 12 TiB 2 particles 13 binder

───────────────────────────────────────────────────── フロントページの続き (72)発明者 市来崎 哲雄 広島県広島市西区観音新町四丁目6番22号 三菱重工業株式会社広島研究所内 (72)発明者 高階 純 東京都千代田区丸の内二丁目5番1号 三 菱重工業株式会社内 ─────────────────────────────────────────────────── ─── Continuation of front page (72) Inventor Tetsuo Ikuzaki 4-6-22 Kannon Shinmachi, Nishi-ku, Hiroshima City, Hiroshima Prefecture Mitsubishi Heavy Industries Ltd. Hiroshima Research Institute (72) Inventor Jun Takashina 2-5 Marunouchi, Chiyoda-ku, Tokyo No. 1 Sanryo Heavy Industries Co., Ltd.

Claims (2)

【特許請求の範囲】[Claims] 【請求項1】 30〜70体積%のTiB2 と、バイン
ダの主成分としてのTiNとの混合粉末を焼結してなる
ことを特徴とするTiB2 セラミックス焼結体。
1. A TiB 2 ceramics sintered body obtained by sintering a mixed powder of 30 to 70% by volume of TiB 2 and TiN as a main component of a binder.
【請求項2】 請求項1のTiB2 セラミックス焼結体
において、バインダの一部をAlN,SiC,TiB2
及びZrO2 より選ばれた一種以上で置換したことを特
徴とするTiB2 セラミックス焼結体。
2. The TiB 2 ceramics sintered body according to claim 1, wherein a part of the binder is AlN, SiC, TiB 2
And a TiB 2 ceramics sintered body characterized by being substituted with one or more selected from ZrO 2 .
JP3282730A 1991-10-29 1991-10-29 Sintered tib2 ceramic Withdrawn JPH05319935A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP3282730A JPH05319935A (en) 1991-10-29 1991-10-29 Sintered tib2 ceramic

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP3282730A JPH05319935A (en) 1991-10-29 1991-10-29 Sintered tib2 ceramic

Publications (1)

Publication Number Publication Date
JPH05319935A true JPH05319935A (en) 1993-12-03

Family

ID=17656301

Family Applications (1)

Application Number Title Priority Date Filing Date
JP3282730A Withdrawn JPH05319935A (en) 1991-10-29 1991-10-29 Sintered tib2 ceramic

Country Status (1)

Country Link
JP (1) JPH05319935A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2007110149A1 (en) * 2006-03-24 2007-10-04 Esk Ceramics Gmbh & Co. Kg Sintered wear-resistant boride material, sinterable powder mixture for producing said material, method for producing the material and use thereof

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2007110149A1 (en) * 2006-03-24 2007-10-04 Esk Ceramics Gmbh & Co. Kg Sintered wear-resistant boride material, sinterable powder mixture for producing said material, method for producing the material and use thereof

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Effective date: 19990107