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JPS6141865B2 - - Google Patents
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JPS6141865B2 - - Google Patents

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Publication number
JPS6141865B2
JPS6141865B2 JP53133299A JP13329978A JPS6141865B2 JP S6141865 B2 JPS6141865 B2 JP S6141865B2 JP 53133299 A JP53133299 A JP 53133299A JP 13329978 A JP13329978 A JP 13329978A JP S6141865 B2 JPS6141865 B2 JP S6141865B2
Authority
JP
Japan
Prior art keywords
ultra
diamond
high pressure
cutting
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.)
Expired
Application number
JP53133299A
Other languages
Japanese (ja)
Other versions
JPS5562852A (en
Inventor
Fumihiro Ueda
Kenichi Nishigaki
Taijiro Oonishi
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 JP13329978A priority Critical patent/JPS5562852A/en
Publication of JPS5562852A publication Critical patent/JPS5562852A/en
Publication of JPS6141865B2 publication Critical patent/JPS6141865B2/ja
Granted legal-status Critical Current

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Description

【発明の詳細な説明】[Detailed description of the invention]

この発明は、すぐれた靭性および耐熱耐摩耗性
を有し、特に切削工具用材料として使用するのに
適した超高圧焼結材料に関するものである。 一般に、鋳鉄などの鉄系金属材料や、アルミニ
ウム、アルミニウム合金、銅、および銅合金など
の非鉄金属材料、さらにプラスチツク、ゴム、黒
鉛、セラミツクなどの非金属材料などの切削に使
用される切削工具には、高硬度、すぐれた耐摩耗
性、靭性、および熱的化学的安定性などの特性を
備えることが要求されている。 近年、かかる要求を満足すべく、主成分がダイ
ヤモンドからなる超高圧焼結材料が提案され、前
記超高圧焼結材料は常温は勿論のこと、比較的高
温においても高硬度を有し、すぐれた耐摩耗性を
示すことから、衝撃の加わるような苛酷な条件下
での仕上げ切削工具用材料として使用されてい
る。 確かに、上記超高圧焼結材料製切削工具によれ
ば、上記鉄系金属材料や非鉄金属材料の切削に際
して、高速切削が可能となるために、構成刃先が
つきにくく、すぐれた仕上げ面が得られるという
利点がもたらされる。 このように上記従来超高圧焼結材料は、主成分
が著しく高い硬さを有するダイヤモンドで構成さ
れているために、上記鉄系金属材料や非鉄金属材
料、および非金属材料の切削に切削工具として使
用した場合に、すぐれた耐摩耗性を示すものの、
十分な靭性を備えたものではないため、この靭性
不足が原因で切削時にチツピング摩耗を起し易
く、この結果本来具備しているすぐれた耐摩耗性
を十分発揮することができず、また十分な高温耐
酸化性を備えていないために、温度上昇を伴なう
切削には使用することができないのが現状であ
る。 本発明者等は、上述のような観点から、靭性、
鉄系金属材料に対する耐反応性、高温耐酸化性
(耐熱性)、および耐摩耗性を兼ね備えた切削工具
用材料を得べく、ダイヤモンドに着目して研究を
行なつた結果、ダイヤモンド粉末に、炭化けい素
(以下SiCで示す)および窒化けい素(以下Si3N4
で示す)のうちの1種または2種(以下これを総
称してSiの炭・窒化物という)からなる粉末と、
立方晶窒化ほう素(以下CBNで示す)粉末とを
配合したものを原料粉末として使用し、超高圧焼
結を行なうと、ダイヤモンド粒子同志、上記Siの
炭・窒化物粒子同志、および上記CBN粒子同志
の相互接触がなく、ダイヤモンド粒子、上記Siの
炭・窒化物粒子、および上記CBN粒子が相互に
隣接し合い、しかもその粒界では前記各粒子を構
成する成分の拡散が生じて強固な粒子間結合が形
成されている緻密な組織の焼結材料が得られ、こ
の結果得られた焼結材料は、ダイヤモンド粒子に
よつてもたらされるすぐれた耐摩耗性と、Siの
炭・窒化物粒子およびCBN粒子によつてもたら
されるすぐれた靫性および高温耐酸化性(耐熱
性)とを兼ね備えるという知見を得たのである。 この発明は、上記知見にもとづいてなされたも
のであつて、容量%で、 ダイヤモンド:50〜85%、 Siの炭・窒化物:5〜40%、 CBN:10〜45%、 からなる組成を有し、かつすぐれた靭性、耐熱
性、および耐摩耗性を有する切削工具用超高圧焼
結材料に特徴を有するものである。 ついで、この発明の超高圧焼結材料において、
成分組成範囲を上述のように限定した理由を説明
する。 (a) ダイヤモンド ダイヤモンド自体は、周知のようにモース硬
さ:10、ヌープ硬さ:8000Kg/mm2以上(荷重100
g)を有し、現存する物質中、最も高い硬さを
有する物質であるが、この含有量が50容量%未
満では、所望の耐摩耗性を確保することができ
ず、一方85容量%を超えて含有させると、ダイ
ヤモンド粒子相互間の接触度合が大きくなり、
特に靭性に富んだSiの炭・窒化物粒子および特
に高温耐酸化性(耐熱性)にすぐれたCBN粒
子と、ダイヤモンド粒子との強固な粒子間結合
が不十分となり、この結果靭性低下をきたして
切削時にチツピング摩耗が生じやすくなること
から、その含有量を50〜85容量%と定めた。 また、この発明の超高圧焼結材料の製造に際
して、原料粉末として使用されるダイヤモンド
粉末は、すぐれた焼結性を確保する目的で、平
均粒径50μm以下、一般には同10μm以下の粉
末粒径をもつものを使用するのが好ましく、さ
らに市販のメタルコートのダイヤモンド粉末を
原料粉末として使用してもよい。 (b) Siの炭・窒化物 例えば、SiCは融点:2827℃、微少ヌープ硬
さ:3000Kg/mm(荷重100g)を有するようにこ
れらSiの炭・窒化物はいずれも高融点高硬度を
有すると共に、ダイヤモンドに比して高温にお
ける耐酸化性にすぐれた物質であり、しかもSi
の炭・窒化物には、この発明の超高圧焼結材料
の製造における焼結時に、上述のようにダイヤ
モンド粒子、Siの炭・窒化物粒子、およびCBN
粒子の相互粒界での成分拡散に寄与して強固な
粒子間結合を形成せしめる作用があるほか、そ
れ自体が焼結性にすぐれたものであるため、ダ
イヤモンド粒子間をCBN粒子と共存した状態
で埋めた緻密な組織を形成する作用があるが、
その含有量が5容量%未満では、前記作用に所
望の効果を得ることができず、この結果靭性低
下をきたすようになり、一方40容量%を超えて
含有させると、相対的にダイヤモンドの含有量
が少なくなり過ぎて、ダイヤモンドのもつ高硬
度を焼結材料に充分反映することができず、こ
の結果耐摩耗性低下をきたすようになることか
ら、その含有量を5〜40容量%に定めた。 また、この発明の超高圧焼結材料の製造に際
して、原料粉末として使用されるSiの炭・窒化
物粉末は微粉のものが好ましく、平均粒径10μ
m以下の微細な粉末を使用するのが望ましい。 (c) CBN CBNは、温度1200℃以上、圧力40Kb以上、
望ましくは温度1800℃以上、圧力60Kb以上の
条件で合成されるもので、ダイヤモンドに次ぐ
硬さ、すなわちビツカース硬さで6000〜7000
Kg/mm2を有し、かつダイヤモンドより高温まで
安定した性質をもつと共に、鉄族金属に対して
反応しにくい性質をもつ成分であるが、その含
有量が10容量%未満では、所望の高温耐酸化性
および鉄系金属に対する耐反応性を確保するこ
とができず、一方45容量%を越えて含有させる
と、相対的にダイヤモンドの含有量が少なくな
り過ぎて、前記ダイヤモンドのもつ高硬度を焼
結材料に充分反映させることができず、この結
果、耐摩耗性の低下をもたらすようになること
からその含有量を10〜45容量%と定めた。 また、この発明の超高圧焼結材料の製造に際
して、原料粉末として使用されるCBN粉末は
微細なものが好ましく、平均粒径10μm以下の
微細粉末の使用が望ましい。 さらに、この発明の超高圧焼結材料は、通常の
粉末冶金法により、公知の超高圧超高温発生装置
を使用して製造することができる。 すなわち、原料粉末としてのダイヤモンド粉
末、Siの炭・窒化物粉末、およびCBN粉末を所定
割合に配合し、この配合粉末を鉄製ボールミルな
どの混合機において長時間混合して均質な混合粉
末とし、ついでこの混合粉末を、例えば特公昭36
−23463号公報に記載されるような超高圧高温発
生装置における鋼製あるいは高融点金属製の容器
内に封入し、圧力および温度を上げ、最高圧力:
54〜70Kb、最高温度:1400〜1800℃の範囲内の
圧力および温度に数分〜数10分保持した後、冷却
し、最終的に圧力を解放することからなる基本的
工程によつて製造することができる。 つぎに、この発明の超高圧焼結材料を実施例に
より説明する。 原料粉末として、それぞれ市販の平均粒径:3
μmを有するダイヤモンド粉末、同3μmのSiC
粉末、同2μmのSi3N4粉末、および同6μmの
CBN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、これに溶媒
としてアセトンを加え、炭化タングステン基超硬
合金製のボールミル中で4時間混合し、乾燥した
後、直径:10mm×高さ:10mmの寸法をもつたステ
ンレス鋼(JIS・SUS304)製管内に詰め、真空引
きしながらJIS・P20の炭化タングステン基超硬
合金等の蓋を前記管の両側端部に溶接して密封
し、ついで、これを公知の超高圧高温発生装置に
装着し、最高付加圧力:60Kb、最高加熱温度:
1450℃の条件で10分間保持して焼結した後、冷却
し、圧力解放を行なうことによつて実質的に配合
組成と同一の成分組成をもつた本発明超高圧焼結
材料1〜9、および比較超高圧焼結材料1〜6を
それぞれ製造した。 この結果得られた本発明超高圧焼結材料1〜9
は、いずれもダイヤモンド、Siの炭・窒化物、お
よびCBNが均一に分散した緻密な組織をもつも
のであつた。 なお、比較超高圧焼結材料1〜6は、いずれも
構成成分のうちの少なくともいずれかの成分含有
量(第1表に※印を付したもの)がこの発明の範
囲から外れた組成をもつものである。 つぎに、上記の本発明超高圧焼結材料1〜9、
および比較超高圧焼結材料1〜6、並びに従来公
知の主成分がダイヤモンドからなる第1表に示さ
れる組成をもつた市販の超高圧焼結材料から、切
断および研磨により切削用切刃を切出し、この切
刃を炭化タングステン基超硬合金製チツプに銀ろ
を用いてろう付けした状態で、
The present invention relates to an ultra-high pressure sintered material that has excellent toughness and heat and wear resistance, and is particularly suitable for use as a material for cutting tools. Generally used for cutting tools used to cut ferrous metal materials such as cast iron, non-ferrous metal materials such as aluminum, aluminum alloys, copper, and copper alloys, and non-metallic materials such as plastics, rubber, graphite, and ceramics. are required to have properties such as high hardness, excellent wear resistance, toughness, and thermal and chemical stability. In recent years, in order to satisfy such demands, ultra-high pressure sintered materials whose main component is diamond have been proposed, and the ultra-high pressure sintered materials have high hardness not only at room temperature but also at relatively high temperatures, and have excellent properties. Because it exhibits wear resistance, it is used as a material for finishing cutting tools under harsh conditions such as impact. It is true that the above-mentioned cutting tool made of ultra-high pressure sintered material enables high-speed cutting when cutting the above-mentioned ferrous metal materials and non-ferrous metal materials, making it difficult for built-up edges to stick and providing an excellent finished surface. This provides the advantage of being able to In this way, the conventional ultra-high pressure sintered materials mentioned above are mainly composed of diamond which has extremely high hardness, so they can be used as cutting tools for cutting the above-mentioned ferrous metal materials, non-ferrous metal materials, and non-metal materials. Although it shows excellent wear resistance when used,
Because it does not have sufficient toughness, chipping wear is likely to occur during cutting due to this lack of toughness, and as a result, the excellent wear resistance that it originally has cannot be fully demonstrated, and the Currently, it cannot be used for cutting that involves a rise in temperature because it does not have high-temperature oxidation resistance. From the above-mentioned viewpoint, the present inventors have determined that toughness,
In order to obtain a material for cutting tools that has resistance to reactions with ferrous metal materials, high-temperature oxidation resistance (heat resistance), and wear resistance, we conducted research focusing on diamond. Silicon (hereinafter referred to as SiC) and silicon nitride (hereinafter referred to as Si 3 N 4
) (hereinafter collectively referred to as Si carbon/nitride);
When a mixture of cubic boron nitride (hereinafter referred to as CBN) powder is used as a raw material powder and ultra-high pressure sintering is performed, diamond particles, Si carbon/nitride particles, and CBN particles are formed. There is no mutual contact between the particles, and the diamond particles, the Si carbon/nitride particles, and the CBN particles are adjacent to each other, and at the grain boundaries, the components that make up each particle diffuse, forming strong particles. A sintered material with a dense structure in which inter-bonds are formed is obtained, and the resulting sintered material has excellent wear resistance provided by diamond particles and Si carbon/nitride particles and They found that it combines the excellent shine and high-temperature oxidation resistance (heat resistance) provided by CBN particles. This invention was made based on the above knowledge, and has a composition consisting of diamond: 50 to 85%, Si carbon/nitride: 5 to 40%, and CBN: 10 to 45% in terms of volume percentage. The ultra-high-pressure sintered material for cutting tools is characterized by having excellent toughness, heat resistance, and wear resistance. Next, in the ultra-high pressure sintered material of this invention,
The reason why the component composition range is limited as described above will be explained. (a) Diamond As is well known, diamond itself has a Mohs hardness of 10 and a Knoop hardness of 8000 kg/mm2 or more (load of 100 kg/mm2).
g), which has the highest hardness among existing materials, but if the content is less than 50% by volume, the desired wear resistance cannot be secured; If the content exceeds the amount, the degree of contact between diamond particles increases,
The strong interparticle bonds between diamond particles and Si carbon/nitride particles, which have particularly high toughness, and CBN particles, which have particularly excellent high-temperature oxidation resistance (heat resistance), are insufficient, resulting in a decrease in toughness. Since chipping wear tends to occur during cutting, the content was set at 50 to 85% by volume. In addition, in the production of the ultra-high pressure sintered material of this invention, the diamond powder used as the raw material powder has an average particle size of 50 μm or less, generally 10 μm or less, in order to ensure excellent sinterability. It is preferable to use diamond powder with a metal coating, and commercially available metal-coated diamond powder may also be used as the raw material powder. (b) Si carbon/nitride For example, SiC has a melting point of 2827°C and a minute Knoop hardness of 3000 Kg/mm (load 100 g). All of these Si carbons and nitrides have high melting points and high hardness. In addition, it is a material with superior oxidation resistance at high temperatures compared to diamond, and it also contains Si.
As mentioned above, diamond particles, Si carbon/nitride particles, and CBN are added to the carbon/nitride particles during sintering in the production of the ultra-high pressure sintered material of the present invention.
In addition to contributing to the diffusion of components at the mutual grain boundaries of the particles and forming strong interparticle bonds, diamond itself has excellent sintering properties, so it can coexist with CBN particles between diamond particles. It has the effect of forming a dense tissue filled with
If the content is less than 5% by volume, the desired effect cannot be obtained, resulting in a decrease in toughness, while if the content exceeds 40% by volume, the diamond content will be relatively low. If the amount becomes too small, the high hardness of diamond cannot be fully reflected in the sintered material, resulting in a decrease in wear resistance. Therefore, the content is set at 5 to 40% by volume. Ta. Furthermore, in producing the ultra-high pressure sintered material of the present invention, the Si carbon/nitride powder used as the raw material powder is preferably fine powder, with an average particle size of 10 μm.
It is desirable to use fine powder of less than m. (c) CBN CBN has a temperature of 1200℃ or more, a pressure of 40Kb or more,
It is preferably synthesized at a temperature of 1,800℃ or higher and a pressure of 60Kb or higher, and has a hardness second only to diamond, i.e., 6,000 to 7,000 on the Vickers hardness.
Kg/mm 2 and has properties that are more stable at higher temperatures than diamond and less reactive to iron group metals. Oxidation resistance and reaction resistance to iron-based metals cannot be ensured, and on the other hand, if the diamond content exceeds 45% by volume, the diamond content becomes relatively too small and the high hardness of diamond is lost. The content was determined to be 10 to 45% by volume because it could not be sufficiently reflected in the sintered material, resulting in a decrease in wear resistance. Further, in producing the ultra-high pressure sintered material of the present invention, the CBN powder used as the raw material powder is preferably fine, and it is desirable to use fine powder with an average particle size of 10 μm or less. Further, the ultra-high pressure sintered material of the present invention can be manufactured by a conventional powder metallurgy method using a known ultra-high pressure and ultra-high temperature generator. That is, diamond powder, Si carbon/nitride powder, and CBN powder as raw material powders are blended in a predetermined ratio, and this blended powder is mixed for a long time in a mixer such as an iron ball mill to form a homogeneous mixed powder. This mixed powder, for example,
It is sealed in a container made of steel or high melting point metal in an ultra-high pressure and high temperature generator as described in Publication No. 23463, and the pressure and temperature are raised to achieve the maximum pressure:
54-70Kb, maximum temperature: 1400-1800℃ Produced by a basic process consisting of holding at a pressure and temperature in the range of several minutes to several tens of minutes, cooling, and finally releasing the pressure. be able to. Next, the ultra-high pressure sintered material of the present invention will be explained using examples. As raw material powder, each commercially available average particle size: 3
Diamond powder with μm, SiC with same 3μm
powder, 2μm Si 3 N 4 powder, and 6μm Si 3 N 4 powder.
Prepare CBN powder, blend these raw powders into the composition shown in Table 1, add acetone as a solvent, mix for 4 hours in a ball mill made of tungsten carbide-based cemented carbide, and then dry. , filled in a stainless steel (JIS/SUS304) tube with dimensions of diameter: 10 mm x height: 10 mm, and while vacuuming, cover both ends of the tube with covers such as JIS/P20 tungsten carbide-based cemented carbide. Welded and sealed, then attached to a known ultra-high pressure and high temperature generator, maximum applied pressure: 60Kb, maximum heating temperature:
The ultra-high pressure sintered materials 1 to 9 of the present invention, which have substantially the same composition as the blended composition, can be obtained by holding and sintering at 1450°C for 10 minutes, cooling, and releasing the pressure. and comparative ultra-high pressure sintered materials 1 to 6 were produced, respectively. The ultra-high pressure sintered materials 1 to 9 of the present invention obtained as a result
All had a dense structure in which diamond, Si carbon/nitride, and CBN were uniformly dispersed. Comparative ultra-high pressure sintered materials 1 to 6 all have compositions in which the content of at least one of the constituent components (marked with * in Table 1) is outside the scope of the present invention. It is something. Next, the above-mentioned ultra-high pressure sintered materials 1 to 9 of the present invention,
Cutting blades were cut by cutting and polishing from Comparative Ultra High Pressure Sintered Materials 1 to 6 and commercially available ultra high pressure sintered materials having the compositions shown in Table 1 whose main component is diamond. , this cutting edge is brazed to a tungsten carbide-based cemented carbide chip using a silver solder,

【表】 被削材:FC30、 切削速度:400m/min、 切込み:0.2mm、 切削油:水溶性油使用、 の条件での鋳鉄の仕上げ面加工切削試験、並びに 被削材:Al−Si合金(Si:30重量%含有)、 切削速度:200m/min、 送り:0.1mm/rev.、 切込み:0.2mm、 切削油:なし、 の条件でのAl合金の仕上げ面加工切削試験を行
ない、いずれの切削試験でも切刃の逃げ面摩耗幅
が0.2mmに達するまでの切削時間を測定した。こ
れらの測定結果を第1表に示した。 第1表に示される結果から、本発明超高圧焼結
材料1〜9は、いずれも市販の超高圧焼結材料に
比して、著しくすぐれた靭性および耐熱性を有
し、かつこれと同等のすぐれた靭性および耐熱性
を有し、かつこれと同等のすぐれた耐摩耗性を有
するので、きわめて長い切削時間を示すのに対し
て、市販の超高圧焼結材料は、靭性および耐熱性
不足が原因で比較的短かい切削時間しか示さない
ことが明らかである。 また、比較超高圧焼結材料1〜6に見られるよ
うに、構成成分のうちの少なくともいずれかの成
分含有量でもこの発明の範囲から外れると、靭
性、耐熱性、および耐摩耗性のうちの少なくとも
いずれかの性質が劣つたものになるので、所望の
切削性能を示さず、比較的短時間の切削時間しか
示さないものである。 上述のように、この発明の超透高圧焼結材料
は、すぐれた靭性、耐熱性(高温耐酸化性)、お
よび耐摩耗性を兼ね備えているので、特に切削工
具用材料として使用した場合にすぐれた切削性能
を発揮するのである。
[Table] Workpiece material: FC30, Cutting speed: 400m/min, Depth of cut: 0.2mm, Cutting oil: Use of water-soluble oil, Cast iron finishing surface machining cutting test under the following conditions, Workpiece material: Al-Si alloy (Contains 30% Si by weight), Cutting speed: 200m/min, Feed: 0.1mm/rev., Depth of cut: 0.2mm, Cutting oil: None. In the cutting test, the cutting time until the flank wear width of the cutting edge reached 0.2 mm was measured. The results of these measurements are shown in Table 1. From the results shown in Table 1, the ultra-high pressure sintered materials 1 to 9 of the present invention all have significantly superior toughness and heat resistance compared to commercially available ultra-high pressure sintered materials, and are equivalent to these. commercially available ultra-high pressure sintered materials lack toughness and heat resistance, and exhibit extremely long cutting times due to their excellent toughness and heat resistance and equally good wear resistance. It is clear that due to this, only a relatively short cutting time is exhibited. Furthermore, as seen in Comparative Ultra-High Pressure Sintered Materials 1 to 6, if the content of at least one of the constituent components falls outside the scope of the present invention, the toughness, heat resistance, and wear resistance may deteriorate. Since at least one of the properties is inferior, it does not exhibit the desired cutting performance and exhibits only a relatively short cutting time. As mentioned above, the ultra-transparent high-pressure sintered material of the present invention has excellent toughness, heat resistance (high-temperature oxidation resistance), and wear resistance, so it is particularly suitable for use as a material for cutting tools. This results in excellent cutting performance.

Claims (1)

【特許請求の範囲】 1 ダイヤモンド:50〜85%、 炭化けい素および窒化けい素のうちの1種また
は2種:5〜40%、 立方晶窒化ほう素および不可避不純物:10〜45
%、 からなる組成(以上容量%)を有することを特徴
とする靭性および耐熱耐摩耗性のすぐれた切削工
具用超高圧焼結材料。
[Claims] 1 Diamond: 50-85%, One or both of silicon carbide and silicon nitride: 5-40%, Cubic boron nitride and inevitable impurities: 10-45
%, an ultra-high pressure sintered material for cutting tools having excellent toughness and heat and wear resistance, characterized by having a composition (volume %) consisting of:
JP13329978A 1978-10-31 1978-10-31 Heattresisting and abrasionnresisting superpressure sintering material with tenacity Granted JPS5562852A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP13329978A JPS5562852A (en) 1978-10-31 1978-10-31 Heattresisting and abrasionnresisting superpressure sintering material with tenacity

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP13329978A JPS5562852A (en) 1978-10-31 1978-10-31 Heattresisting and abrasionnresisting superpressure sintering material with tenacity

Publications (2)

Publication Number Publication Date
JPS5562852A JPS5562852A (en) 1980-05-12
JPS6141865B2 true JPS6141865B2 (en) 1986-09-18

Family

ID=15101401

Family Applications (1)

Application Number Title Priority Date Filing Date
JP13329978A Granted JPS5562852A (en) 1978-10-31 1978-10-31 Heattresisting and abrasionnresisting superpressure sintering material with tenacity

Country Status (1)

Country Link
JP (1) JPS5562852A (en)

Also Published As

Publication number Publication date
JPS5562852A (en) 1980-05-12

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