JPS58145676A - Surface-clad silicon nitride base sintered member for high speed cutting tool - Google Patents

Surface-clad silicon nitride base sintered member for high speed cutting tool

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Publication number
JPS58145676A
JPS58145676A JP2696182A JP2696182A JPS58145676A JP S58145676 A JPS58145676 A JP S58145676A JP 2696182 A JP2696182 A JP 2696182A JP 2696182 A JP2696182 A JP 2696182A JP S58145676 A JPS58145676 A JP S58145676A
Authority
JP
Japan
Prior art keywords
cutting
silicon
silicon nitride
oxide
sintered member
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
Application number
JP2696182A
Other languages
Japanese (ja)
Other versions
JPS6240319B2 (en
Inventor
杉澤 泰次郎
照義 棚瀬
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 Metal Corp
Original Assignee
Mitsubishi Metal Corp
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 Metal Corp filed Critical Mitsubishi Metal Corp
Priority to JP2696182A priority Critical patent/JPS58145676A/en
Publication of JPS58145676A publication Critical patent/JPS58145676A/en
Publication of JPS6240319B2 publication Critical patent/JPS6240319B2/ja
Granted 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】 この発明は、すぐれた耐摩耗性、耐熱衝撃性。[Detailed description of the invention] This invention has excellent abrasion resistance and thermal shock resistance.

および高温強度を有し、特にこれらの特性が要求される
鋼および鋳鉄の高速切削に切削工具として使用した場合
にすぐれた切削性能を発揮する表面被覆窒化けい素基焼
結部材に関するものである。
The present invention also relates to a surface-coated silicon nitride-based sintered member that has high-temperature strength and exhibits excellent cutting performance when used as a cutting tool for high-speed cutting of steel and cast iron, which particularly require these properties.

近年、被剛材としての鋼および鋳鉄の高速切削を可能と
すべく種々の研究開発が試みられ、なかでも工作機械の
高剛性化と切削工具材料の改善の両面から、これら被剛
材の高速切削への移行は着々と達成されつつあり、現時
点では300〜600m/mjnの高い切削速度での安
定した切削が1つの目標とされている。
In recent years, various research and development efforts have been made to enable high-speed cutting of steel and cast iron as rigid materials. The transition to cutting is steadily being achieved, and at present one of the goals is stable cutting at a high cutting speed of 300 to 600 m/mjn.

なお、上記の高い切削速度は、高速切削時に発生する熱
に対してすぐれた耐酸化性を示すと共に、Feとの化学
的反応性が低く、かつ摩擦係数の小さな酸化アルミニウ
ム(以下A9□03で示す)を主成分として含有するA
e203基焼結材別を切削工具として使用するという前
提で、高速切削を可能とすべく工作機械に改良を加える
ことによって達成できるとして定められたものである。
The above-mentioned high cutting speed is achieved by using aluminum oxide (hereinafter referred to as A9□03), which has excellent oxidation resistance against the heat generated during high-speed cutting, has low chemical reactivity with Fe, and has a small friction coefficient. A containing as a main component
It was determined that this can be achieved by improving machine tools to enable high-speed cutting, on the premise that e203 sintered materials will be used as cutting tools.

しかしながら、上記のM2O3基焼結材料は、十分な耐
熱衝撃性および高温における機械的強度を備えていない
ために、これを切削工具として、特に鋼の切削に300
〜600m/mI7+の高い切削速度で使用した場合、
工作機械の改良も未だ不十分であることと相まって安定
した切削性能を発揮し得ないのが現状である。
However, the above M2O3-based sintered material does not have sufficient thermal shock resistance and mechanical strength at high temperatures, so it is used as a cutting tool, especially for cutting steel.
When used at high cutting speeds of ~600m/mI7+,
Coupled with the fact that machine tools have not yet been sufficiently improved, stable cutting performance cannot currently be achieved.

また、一方、熱膨張係数が小さく、すなわち耐熱衝撃性
にすぐれ、かつ高温における機械的強度にもすぐれた窒
化けい素(以下Si3N4で示す)や513N4にAQ
20.が固溶したものからなるザイアロン(以下5i3
N4(A北203)で示す)を主成分とし、かつ酸化イ
ツトリウム(以下¥203で示す)、酸化マグネシウム
(以下M g Oで示す)、酸化けい素(以下5102
で示す)、窒化アルミニウム(以下AQ Nで示す)、
酸化チタン(以下TlO2で示す)。
On the other hand, silicon nitride (hereinafter referred to as Si3N4) and 513N4, which have a small coefficient of thermal expansion, that is, excellent thermal shock resistance and excellent mechanical strength at high temperatures,
20. Xialon (hereinafter referred to as 5i3) consisting of a solid solution of
The main component is N4 (denoted as A Kita 203)), and also contains yttrium oxide (hereinafter referred to as ¥203), magnesium oxide (hereinafter referred to as MgO), and silicon oxide (hereinafter referred to as 5102).
), aluminum nitride (hereinafter referred to as AQN),
Titanium oxide (hereinafter referred to as TlO2).

酸化ジルコニウム(以下ZrO,,で示す)、および酸
化ハフニウム(以下HfO□で示す)のうちの1種また
は2種以上からなる結合相形成成分を1〜30重量係含
有する813N4基焼結材料を、鋼および鋳鉄の高速切
削に切削工具として使用する試みもなされているが、こ
のSi3N、基焼結材料は、Feとの反応性が高いため
に、特に鋼の高速切削に際しては、摩耗が激しく、切削
工具としては汎用性のきわめて低いものである。
An 813N 4-based sintered material containing 1 to 30 by weight of a binder phase forming component consisting of one or more of zirconium oxide (hereinafter referred to as ZrO) and hafnium oxide (hereinafter referred to as HfO□). Attempts have also been made to use this Si3N-based sintered material as a cutting tool for high-speed cutting of steel and cast iron, but this Si3N-based sintered material has high reactivity with Fe, so it wears severely, especially when cutting steel at high speed. , it has extremely low versatility as a cutting tool.

そこで、本発明者等は、上述のような観点から、すぐれ
た耐熱衝撃性および高温強度を有するが、特に鋼の高速
切削に切削工具として使用した場合、摩耗が激しく、実
用に供し得ない上記の従来813 N4基焼結材料に着
目し、これにすぐれた耐摩耗性を付与すべく研究を行な
った結果、前記従来Si3N4基焼結材料の基体表面に
、窒化けい素(以下、(Si)Nで示す)、酸窒化けい
素(以下(Si)ONで示す)、炭窒化けい素(以下(
Sj、)CNで示す)。
Therefore, from the above-mentioned viewpoints, the present inventors have discovered that although the tool has excellent thermal shock resistance and high-temperature strength, when used as a cutting tool especially for high-speed cutting of steel, it suffers from severe wear and cannot be put to practical use. Focusing on the conventional 813N4-based sintered material, we conducted research to give it excellent wear resistance.As a result, we found that silicon nitride (hereinafter referred to as (Si)) was added to the base surface of the conventional Si3N4-based sintered material. silicon oxynitride (hereinafter referred to as (Si)ON), silicon carbonitride (hereinafter referred to as (Si)ON), silicon oxynitride (hereinafter referred to as (Si)ON),
Sj,) denoted by CN).

炭酸窒化けい素(以下(Si )CONで示す)、At
!固溶の窒化けい素(以下(Si、 A+り Nで示す
)、AA固溶の酸窒化けい素(以下(Si、 AA)O
Nf示す)、AQ固溶の炭窒化けい素(以下(si、A
Q)c”Nで示す)、およびAQ、固溶の炭酸窒化けい
素(以下(Si、 AM)CONで示し、−以上の各成
分を総称して5i−N系化合物という)のうちの1種の
単層または2種以上の複層からなる化学蒸着皮膜を05
〜10.0μmの平均層厚で被覆すると、前記5i−N
系化合物の化学蒸着皮膜は、前記基体表面との密着性が
著しく高く、かつすぐれた耐摩耗性を有しているので、
この結果の表面被覆Si3N4基焼結部材は、これを鋼
および鋳鉄の切削に切削工具として使用した場合、30
0 m 1m1n以上の高速切削において著しくすぐれ
た切削性能を安定して発揮するようになシ、さらに必要
に応じて上記の5i−N系化合物の化学蓋 5 − 着皮膜の上に、外層としてAt203層層を05〜50
μmの平均層厚で被覆すると、このA2203層は前記
5i−N系化合物層との付着強度が高く、しかもAt2
03層は高速切削に際して、すぐれた耐酸化性および耐
摩耗性を示すことから、工具寿命の一段の延命がはかれ
るようになるという知見を得たのである。
Silicon carbonate nitride (hereinafter referred to as (Si)CON), At
! Solid solution silicon nitride (hereinafter referred to as (Si, A+N)), AA solid solution silicon oxynitride (hereinafter (Si, AA) O)
Nf), AQ solid solution silicon carbonitride (hereinafter (si, A
Q)c''N), and AQ, solid solution silicon carbonate nitride (hereinafter referred to as (Si, AM)CON, - the above components are collectively referred to as 5i-N compounds). A chemical vapor deposition film consisting of a single layer of seeds or a multilayer of two or more seeds is 05
When coated with an average layer thickness of ~10.0 μm, the 5i-N
The chemical vapor deposited film of the based compound has extremely high adhesion to the substrate surface and has excellent wear resistance.
The resultant surface-coated Si3N4-based sintered member can be used as a cutting tool for cutting steel and cast iron.
In order to stably exhibit outstanding cutting performance in high-speed cutting of 0 m 1 m 1 nm or more, a chemical cap of the above-mentioned 5i-N compound is added as necessary. Layer 05-50
When coated with an average layer thickness of μm, this A2203 layer has high adhesion strength with the 5i-N compound layer, and
Since the 03 layer exhibits excellent oxidation resistance and wear resistance during high-speed cutting, it was discovered that the tool life can be further extended.

この発明は、上記知見にもとづいてなされたものであっ
て、以下に基体の成分組成、並びに5i−N系化合物皮
膜およびAQ203皮膜の平均層厚を上記の通りに限定
した理由を説明する。
This invention was made based on the above findings, and the reason why the component composition of the substrate and the average layer thickness of the 5i-N compound film and the AQ203 film were limited as described above will be explained below.

(a)  基体の成分組成 Y2O3,MgO,5i02. AQN 、 TiO2
,ZrO2,およびHfO2の結合相形成成分には、基
体の焼結性と靭性を向上させる作用があるが、その含有
量が1重量φ未満では、前記作用に所望の効果が得られ
ず、一方30重量係を越えて含有させると、相対的に5
t3N4および5i3N4(A1203 )の含有量が
少なくなりすぎて基体の耐熱衝撃性および高温強度が低
下するようになることから、その含有量を1〜3〇 6
− 重量係と定めた。
(a) Component composition of the substrate Y2O3, MgO, 5i02. AQN, TiO2
, ZrO2, and HfO2 have the effect of improving the sinterability and toughness of the substrate, but if their content is less than 1 weight φ, the desired effect cannot be obtained; If the content exceeds 30% by weight, the relative
If the content of t3N4 and 5i3N4 (A1203) becomes too low, the thermal shock resistance and high temperature strength of the substrate will decrease, so the content should be reduced from 1 to 30 6
- Defined as weight department.

(b)Si−N系化合物の平均層厚 上記の通り、5i−N系化合物の化学蒸着皮膜は、Si
3N4基焼結材料の基体表面との結合力がきわめて強固
で、かつすぐれた耐摩耗性を有するものであるため、前
記5i−N系化合物の化学蒸着皮膜によって被覆された
Si3N4基焼結部材は鋳鉄切削は勿論のこと、鋼の高
速切削においてもすぐれた耐摩耗性を示すが、その平均
層厚が05μm未満では、所望の耐摩耗性を確保するこ
とができず、一方10.0μmを越えて厚くしてもより
一層の耐摩耗性向上効果は得られないことから、その平
均層厚を05〜10.0/Zmと定めた。
(b) Average layer thickness of Si-N compound As mentioned above, the chemical vapor deposition film of 5i-N compound is
Since the bonding force of the 3N4 base sintered material with the substrate surface is extremely strong and it has excellent wear resistance, the Si3N4 base sintered member coated with the chemical vapor deposition film of the 5i-N compound is It exhibits excellent wear resistance not only in cast iron cutting but also in high-speed cutting of steel. However, if the average layer thickness is less than 0.05 μm, the desired wear resistance cannot be secured; on the other hand, if it exceeds 10.0 μm, Even if the layer thickness is made thicker, the effect of further improving wear resistance cannot be obtained, so the average layer thickness is set at 05 to 10.0/Zm.

(CI  At!203  の平均層厚上記の通り、A
9203の化学蒸着皮膜は、上記のSi−N系化合物の
化学蒸着皮膜との結合力が非常に強く、かつ自身もすぐ
れた耐酸化性および耐摩耗性を有するものであるので、
AQ203皮膜を外層として形成することによって一層
の切削寿命の延命化がはかれるように々るが、その平均
層厚が05μ7n未満では所望の向上効果が得られず、
一方5.0μmを越えて厚くすると、部材自体の靭性が
低下するようになることから、その平均層厚を05〜5
0μmと定めた。
(Average layer thickness of CI At!203 As above, A
The chemical vapor deposited film of 9203 has a very strong bond with the chemical vapor deposited film of the Si-N compound mentioned above, and also has excellent oxidation resistance and wear resistance.
By forming an AQ203 film as an outer layer, the cutting life can be further extended, but if the average layer thickness is less than 0.5 μm, the desired improvement effect cannot be obtained.
On the other hand, if the thickness exceeds 5.0 μm, the toughness of the member itself will decrease, so the average layer thickness should be adjusted to 0.5 to 5 μm.
It was set as 0 μm.

さらに、この発明の表面被覆S1.N4基焼結部材にお
ける焼結基体は、原料粉末を所定の配合組成に配合し、
混合し、普通焼結あるいはホットプレスを適用すること
によって製造することができ、この場合前記基体は抗折
強度ニア0kg/−以上。
Furthermore, the surface coating S1 of this invention. The sintered base of the N4-based sintered member is made by blending raw material powder into a predetermined composition,
It can be manufactured by mixing and applying normal sintering or hot pressing, in which case the substrate has a transverse strength of near 0 kg/- or more.

ビッカース硬さ 1600kg/−以上をもつものとな
り、さらに前記基体表面に被覆される5i−N系化合物
およびAg、203の化学蒸着皮膜は、通常の化学蒸着
法(望ましくはプラズマ化学蒸着法がよい)にしたがい
、反応ガスとして、塩化シラン。
It has a Vickers hardness of 1,600 kg/- or more, and the chemical vapor deposition film of the 5i-N compound and Ag, 203 coated on the surface of the substrate is formed by a normal chemical vapor deposition method (preferably a plasma chemical vapor deposition method). According to the reaction gas, chlorosilane.

メチル塩化シラン、モノシラン、アンモニア、N2ガス
、3塩化アルミニウム、アセチレン、メタン。
Methyl chloride silane, monosilane, ammonia, N2 gas, aluminum trichloride, acetylene, methane.

COガス、C02ガス、およびH20々と、ギヤリヤー
ガスとしてN2ガスを用い、これら反応ガスを適宜選択
糾合せて使用することによって所定組成の]一層または
2層以上のものを形成することができる。
By using CO gas, CO2 gas, H20, and N2 gas as a gear gas, and by appropriately selecting and combining these reaction gases, one layer or two or more layers of a predetermined composition can be formed.

つぎに、この発明の表面被覆Si3N4基焼結部材を実
施例により具体的に説明する。
Next, the surface-coated Si3N4-based sintered member of the present invention will be specifically explained with reference to Examples.

実施例 原料粉末として、いずれも市販の平均粒径°]〜2μm
を有するY2O3粉末、  MgO粉末、 5in2粉
末。
All of the raw material powders used in the examples had commercially available average particle diameters of ~2 μm.
Y2O3 powder, MgO powder, 5in2 powder with.

AQN粉末、 TiO2粉末、 ZrO2粉末、 Hf
○2粉末+513N4粉末、および5i3N4(Al2
O3)粉末を用意し、これら原料粉末をそれぞれ第1表
に示される配合組成に配合し、湿式ボールミルにて十分
に混合し、乾燥した後、黒鉛型を用い、温度:1700
〜1900℃、圧カニ 100〜250 kg/ffl
 、保持時間。
AQN powder, TiO2 powder, ZrO2 powder, Hf
○2 powder + 513N4 powder, and 5i3N4 (Al2
O3) Prepare powder, mix these raw material powders to the composition shown in Table 1, mix thoroughly in a wet ball mill, dry, and then use a graphite mold at a temperature of 1700.
~1900℃, pressure crab 100~250 kg/ffl
, retention time.

30〜60分の条件でホットプレスすることによって、
実質的に配合組成と同一の最終成分組成を有するSi3
N4基焼結材料基体を製造し、ついで前記基体に研削を
施してISO規格5NO−N432型の切削チップとし
た後、所定のホーニングを刃先に施し、引続いて公知の
化学蒸着装置を用い、それぞれ第1表に示される材質お
よび平均層厚の81−N系化合物皮膜およびAM203
皮膜を形成することによって本発明表面被覆切削チップ
1〜23を 9− 製造した。なお、上記の表面被覆を施さない切削チップ
のうちの5種を比較切削チップ1〜5として用意した。
By hot pressing for 30 to 60 minutes,
Si3 having a final component composition substantially the same as the formulation composition
After manufacturing an N4-based sintered material base and then grinding the base to obtain a cutting tip of the ISO standard 5NO-N432 type, a prescribed honing is performed on the cutting edge, and subsequently using a known chemical vapor deposition device, 81-N compound film and AM203 having the materials and average layer thickness shown in Table 1, respectively.
Surface-coated cutting chips 1 to 23 of the present invention were manufactured by forming a film. Incidentally, five types of cutting chips without surface coating were prepared as comparison cutting chips 1 to 5.

ついで、この結果得られた本発明表面被覆切削チップ]
〜23および比較切削チップ1〜5について、被削材:
 SNCM−8(ブリネル硬さ:2’70)。
Then, the surface-coated cutting tip of the present invention obtained as a result]
~23 and comparative cutting tips 1 to 5, workpiece material:
SNCM-8 (Brinell hardness: 2'70).

切削速度: 300 m / mm 、切込み:]、5
mm+送り: 0.35 g/ rev、の条件での鋼
高速連続切削試験。
Cutting speed: 300 m/mm, depth of cut: ], 5
Steel high-speed continuous cutting test under the conditions of mm+feed: 0.35 g/rev.

および被削材:FC−25(ブリネル硬さ: 150)
And work material: FC-25 (Brinell hardness: 150)
.

切削速度:z5om7m=、送り: 0.25 m@/
rev、。
Cutting speed: z5om7m=, Feed: 0.25m@/
rev.

切込み:2mmの条件での鋳鉄高速連続切削試験を行な
い、それぞれフランク摩耗幅が0.3 m、に至るまで
の寿命時間を測定した。これらの測定結果を第1表に合
せて示した。
A cast iron high-speed continuous cutting test was conducted under the condition of cutting depth: 2 mm, and the life time until the flank wear width reached 0.3 m was measured. These measurement results are also shown in Table 1.

第1表に示される結果から明らかなように、本発明表面
被覆切削チップ1−23は、いずれもすぐれた耐摩耗性
、耐熱衝撃性、および高温強度をもつことから、鋼およ
び鋳鉄の高速切削においてきわめて長い切削寿命を示す
のに対して、化学蒸着皮膜の形成が々いために耐摩耗性
の劣ったものになっている比較切削チップ1〜5におい
ては、相対的に短かい切削寿命しか示さないのである。
As is clear from the results shown in Table 1, surface-coated cutting inserts 1-23 of the present invention have excellent wear resistance, thermal shock resistance, and high-temperature strength, so they can be used for high-speed cutting of steel and cast iron. In contrast, Comparative Cutting Tips 1 to 5, which have poor wear resistance due to extensive chemical vapor deposition film formation, only show relatively short cutting lives. There isn't.

上述のように、この発明の表面被覆Si3N4基焼結部
材によれば、その基体によってすぐれた耐熱衝撃性と高
温強度が確保され、かつ前記基体表面との結合力および
外層としてのAQ、03  皮膜との結合力が著しく強
固なSj、−N系化合物皮膜、並びに前記AQ203皮
膜によってすぐれた耐摩耗性が確保されるので、これを
これらの特性が要求される鋼および鋳鉄の高速切削に切
削工具として使用すれば、きわめてすぐれた切削性能を
長期に亘って安定して発揮するようになるなどの工業上
有用な効果がもたらされるのである。
As described above, according to the surface-coated Si3N4-based sintered member of the present invention, the base body ensures excellent thermal shock resistance and high-temperature strength, and the bonding strength with the base surface and the AQ, 03 coating as the outer layer are maintained. Excellent wear resistance is ensured by the Sj, -N-based compound film, which has an extremely strong bonding force with the AQ203 film, and it is suitable for cutting tools for high-speed cutting of steel and cast iron, which require these properties. When used as a cutting agent, industrially useful effects such as extremely excellent cutting performance can be achieved stably over a long period of time.

出願人  三菱金属株式会社 代理人  富  1) 和 夫Applicant: Mitsubishi Metals Corporation Agent Tomi 1) Kazuo

Claims (2)

【特許請求の範囲】[Claims] (1)  酸化イツトリウム、酸化マグネシウム、酸化
けい素、窒化アルミニウム、酸化チタン、酸化ジルコニ
ウム、および酸化ハフニウムのうちの1種または2種以
上:1〜30重量係重量布し、残シが窒化けい素および
サイアロンのうちの1種または2種と不可避不純物から
なる組成を有する窒化けい素基焼結基体の表面に、窒化
けい素、酸窒化けい素、炭窒化けい素、炭酸窒化けい素
、 AA固溶の窒化けい素、NV、固溶の酸窒化けい素
1M固溶の炭窒化けい素、およびM固溶の炭酸窒化けい
素のうちの1種の単層または2種以上の複層からなる化
学蒸着皮膜を05〜10.0μmの平均層厚で被覆して
なる高速切削工具用表面被覆窒化けい素基焼結部材。
(1) One or more of yttrium oxide, magnesium oxide, silicon oxide, aluminum nitride, titanium oxide, zirconium oxide, and hafnium oxide: 1 to 30 weight coefficients, with the remainder being silicon nitride. Silicon nitride, silicon oxynitride, silicon carbonitride, silicon carbonate nitride, AA solid Consisting of a single layer or a multilayer of two or more of the following: silicon nitride in solution, NV, silicon oxynitride in solid solution, silicon carbonitride in 1M solid solution, and silicon carbonitride in M solid solution A surface-coated silicon nitride-based sintered member for a high-speed cutting tool, which is coated with a chemical vapor deposition film with an average layer thickness of 05 to 10.0 μm.
(2)上記特許請求の範囲第(月項記載の表面被覆窒化
けい素基焼結部材において、上記化学蒸着皮膜の上に、
さらに外層として酸化アルミニウムからなる化学蒸着皮
膜を05〜50μmの平均層厚で被覆してなる高速切削
工具用表面被覆窒化けい素基焼結部材。
(2) In the surface-coated silicon nitride-based sintered member according to claim 1, on the chemical vapor deposition film,
A surface-coated silicon nitride-based sintered member for a high-speed cutting tool, further comprising a chemical vapor deposition film of aluminum oxide with an average layer thickness of 05 to 50 μm as an outer layer.
JP2696182A 1982-02-22 1982-02-22 Surface-clad silicon nitride base sintered member for high speed cutting tool Granted JPS58145676A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP2696182A JPS58145676A (en) 1982-02-22 1982-02-22 Surface-clad silicon nitride base sintered member for high speed cutting tool

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP2696182A JPS58145676A (en) 1982-02-22 1982-02-22 Surface-clad silicon nitride base sintered member for high speed cutting tool

Publications (2)

Publication Number Publication Date
JPS58145676A true JPS58145676A (en) 1983-08-30
JPS6240319B2 JPS6240319B2 (en) 1987-08-27

Family

ID=12207747

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2696182A Granted JPS58145676A (en) 1982-02-22 1982-02-22 Surface-clad silicon nitride base sintered member for high speed cutting tool

Country Status (1)

Country Link
JP (1) JPS58145676A (en)

Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0227471A2 (en) * 1985-12-25 1987-07-01 Kabushiki Kaisha Toshiba Sintered silicon nitride ceramic article
JPS62162683A (en) * 1986-01-14 1987-07-18 住友電気工業株式会社 Coated silicon nitride product
JPS6340786A (en) * 1986-08-01 1988-02-22 住友電気工業株式会社 Manufacture of coated ceramic tool
WO1988009315A1 (en) * 1987-05-19 1988-12-01 Kennametal Inc. Sialon cutting tool composition
US4880755A (en) * 1987-05-19 1989-11-14 Kennametal Inc. Sialon cutting tool composition
US4892848A (en) * 1985-07-30 1990-01-09 Kyocera Corporation Silicon nitride sintered body and process for preparation thereof
US4913936A (en) * 1987-05-19 1990-04-03 Kennametal Inc. Method of surface alloying sialon articles

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS56155080A (en) * 1980-04-30 1981-12-01 Sumitomo Electric Industries Coated cutting tool
JPS5716162A (en) * 1980-07-02 1982-01-27 Sumitomo Electric Ind Ltd Coated cutting tool

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS56155080A (en) * 1980-04-30 1981-12-01 Sumitomo Electric Industries Coated cutting tool
JPS5716162A (en) * 1980-07-02 1982-01-27 Sumitomo Electric Ind Ltd Coated cutting tool

Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4892848A (en) * 1985-07-30 1990-01-09 Kyocera Corporation Silicon nitride sintered body and process for preparation thereof
EP0227471A2 (en) * 1985-12-25 1987-07-01 Kabushiki Kaisha Toshiba Sintered silicon nitride ceramic article
JPS62162683A (en) * 1986-01-14 1987-07-18 住友電気工業株式会社 Coated silicon nitride product
JPS6340786A (en) * 1986-08-01 1988-02-22 住友電気工業株式会社 Manufacture of coated ceramic tool
WO1988009315A1 (en) * 1987-05-19 1988-12-01 Kennametal Inc. Sialon cutting tool composition
US4880755A (en) * 1987-05-19 1989-11-14 Kennametal Inc. Sialon cutting tool composition
US4913936A (en) * 1987-05-19 1990-04-03 Kennametal Inc. Method of surface alloying sialon articles

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