JPS602379B2 - Cubic boron nitride-based ultra-high pressure sintered material for cutting and wear-resistant tools - Google Patents
Cubic boron nitride-based ultra-high pressure sintered material for cutting and wear-resistant toolsInfo
- Publication number
- JPS602379B2 JPS602379B2 JP56211466A JP21146681A JPS602379B2 JP S602379 B2 JPS602379 B2 JP S602379B2 JP 56211466 A JP56211466 A JP 56211466A JP 21146681 A JP21146681 A JP 21146681A JP S602379 B2 JPS602379 B2 JP S602379B2
- Authority
- JP
- Japan
- Prior art keywords
- cutting
- wear
- high pressure
- powder
- boron nitride
- 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
Links
- 239000000463 material Substances 0.000 title claims description 28
- 229910052582 BN Inorganic materials 0.000 title claims 3
- PZNSFCLAULLKQX-UHFFFAOYSA-N Boron nitride Chemical compound N#B PZNSFCLAULLKQX-UHFFFAOYSA-N 0.000 title claims 3
- 150000004767 nitrides Chemical class 0.000 claims description 7
- 229910052759 nickel Inorganic materials 0.000 claims description 5
- 238000005299 abrasion Methods 0.000 claims description 4
- 229910052763 palladium Inorganic materials 0.000 claims description 3
- 229910052715 tantalum Inorganic materials 0.000 claims description 3
- 229910052719 titanium Inorganic materials 0.000 claims description 3
- 229910052726 zirconium Inorganic materials 0.000 claims description 3
- 239000012535 impurity Substances 0.000 claims description 2
- 150000001247 metal acetylides Chemical class 0.000 claims description 2
- 239000006104 solid solution Substances 0.000 claims description 2
- 229910052721 tungsten Inorganic materials 0.000 claims description 2
- 239000000843 powder Substances 0.000 description 23
- 230000000694 effects Effects 0.000 description 7
- 239000011230 binding agent Substances 0.000 description 6
- 239000000203 mixture Substances 0.000 description 6
- 229910052751 metal Inorganic materials 0.000 description 5
- 239000002184 metal Substances 0.000 description 5
- 230000000052 comparative effect Effects 0.000 description 4
- 239000002245 particle Substances 0.000 description 4
- 230000001737 promoting effect Effects 0.000 description 4
- 229910045601 alloy Inorganic materials 0.000 description 3
- 239000000956 alloy Substances 0.000 description 3
- 229910000997 High-speed steel Inorganic materials 0.000 description 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical group [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- 239000000919 ceramic Substances 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 239000000470 constituent Substances 0.000 description 2
- 230000007423 decrease Effects 0.000 description 2
- 229910021404 metallic carbon Inorganic materials 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- 239000002994 raw material Substances 0.000 description 2
- 241000894007 species Species 0.000 description 2
- 239000010936 titanium Substances 0.000 description 2
- 238000003466 welding Methods 0.000 description 2
- ITWBWJFEJCHKSN-UHFFFAOYSA-N 1,4,7-triazonane Chemical compound C1CNCCNCCN1 ITWBWJFEJCHKSN-UHFFFAOYSA-N 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- 229910020630 Co Ni Inorganic materials 0.000 description 1
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 1
- 241000269821 Scombridae Species 0.000 description 1
- 229910000831 Steel Inorganic materials 0.000 description 1
- NRTOMJZYCJJWKI-UHFFFAOYSA-N Titanium nitride Chemical group [Ti]#N NRTOMJZYCJJWKI-UHFFFAOYSA-N 0.000 description 1
- 230000032683 aging Effects 0.000 description 1
- 238000000137 annealing Methods 0.000 description 1
- 210000004556 brain Anatomy 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 230000001112 coagulating effect Effects 0.000 description 1
- 230000002860 competitive effect Effects 0.000 description 1
- PMHQVHHXPFUNSP-UHFFFAOYSA-M copper(1+);methylsulfanylmethane;bromide Chemical compound Br[Cu].CSC PMHQVHHXPFUNSP-UHFFFAOYSA-M 0.000 description 1
- 239000010730 cutting oil Substances 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- 239000010419 fine particle Substances 0.000 description 1
- 230000020169 heat generation Effects 0.000 description 1
- 235000020640 mackerel Nutrition 0.000 description 1
- 238000003801 milling Methods 0.000 description 1
- 238000000465 moulding Methods 0.000 description 1
- 210000003205 muscle Anatomy 0.000 description 1
- 229910001235 nimonic Inorganic materials 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- TWNQGVIAIRXVLR-UHFFFAOYSA-N oxo(oxoalumanyloxy)alumane Chemical compound O=[Al]O[Al]=O TWNQGVIAIRXVLR-UHFFFAOYSA-N 0.000 description 1
- 239000011148 porous material Substances 0.000 description 1
- 238000005245 sintering Methods 0.000 description 1
- 239000010959 steel Substances 0.000 description 1
- 229910000601 superalloy Inorganic materials 0.000 description 1
- MTPVUVINMAGMJL-UHFFFAOYSA-N trimethyl(1,1,2,2,2-pentafluoroethyl)silane Chemical compound C[Si](C)(C)C(F)(F)C(F)(F)F MTPVUVINMAGMJL-UHFFFAOYSA-N 0.000 description 1
- UONOETXJSWQNOL-UHFFFAOYSA-N tungsten carbide Chemical compound [W+]#[C-] UONOETXJSWQNOL-UHFFFAOYSA-N 0.000 description 1
- 238000005491 wire drawing Methods 0.000 description 1
Description
【発明の詳細な説明】
この発明は、すぐれた靭‘性と耐摩耗性とを兼ね備え、
かつ高硬度と、すぐれた耐熱性および高温強度を備え、
特にこれらの特性が要求されるNi基あるいはCo基ス
ーパーアロィや高速度鋼などの被削村の切削工具用とし
て、さらに軸受や線引きダイスなどの耐摩耗工具用とし
て使用するのに通した立方晶窒化棚素基超高圧競鯖材料
に関するものである。[Detailed description of the invention] This invention combines excellent toughness and wear resistance,
It also has high hardness, excellent heat resistance and high temperature strength,
Especially for cutting tools that require these properties such as Ni-based or Co-based super alloys and high-speed steel, and for wear-resistant tools such as bearings and wire drawing dies. This paper relates to crystalline nitride shelbase-based ultra-high-pressure competitive mackerel materials.
近年、炭化タングステン基焼綾材料に比して、きわめて
すぐれた耐摩耗性を有する立方晶窒化棚秦基超高圧暁結
材料(以下CBN基凝結材料と略記する)が切削工具や
耐摩耗工具として使用される傾向にある。In recent years, cubic nitride terrace-based ultra-high-pressure agglomerated materials (hereinafter abbreviated as CBN-based agglomerated materials), which have extremely superior wear resistance compared to tungsten carbide-based sintered twill materials, have been used as cutting tools and wear-resistant tools. tend to be used.
このCBN基鱗縞材料は、分散相を形成するCBN粒子
の結合相によって2種類に大別することができ、その1
つが結合相を鉄族金属、あるいは鉄族金属とNなどを主
成分とする金属で構成したものであり、もう1つが窒化
チタン、炭化チタン、窒化アルミニウム、または酸化ア
ルミニウムなどを主成分として含有するセラミック系化
合物で結合相を構成したものである。This CBN-based scale-stripe material can be roughly divided into two types depending on the binder phase of CBN particles forming the dispersed phase.
One is one in which the binder phase is composed of an iron group metal, or a metal whose main component is an iron group metal and N, and the other one is one whose main component is titanium nitride, titanium carbide, aluminum nitride, or aluminum oxide. The bonding phase is made of a ceramic compound.
しかしながら、前者においては、上記のように結合相が
金属であるため高靭性をもつものの高温で軟化しやすく
、したがって、これを例えば切削工具として使用した場
合には多大な熱発生を伴う苛酷な切削条件下では耐摩耗
性および耐溶着性不足をきたして十分なる切削性能の発
揮は期待できず、熱発生の少ない条件、すなわち負荷の
少ない条件でしか使用することができないものである。
また、後者においては、上記のように結合相がセラミッ
ク系化合物で構成されているために、耐摩耗性および耐
溶着性のすぐれたものになっているが、反面轍性不足を
避けることができず、例えば高速度鋼のフライス切削な
どの刃先に大きな衝撃力の加わる切削条件下ではチツピ
ングや欠損を起し易いものである。そこで、本発明者等
は、上述のような観点から、靭性および耐摩耗性を兼ね
備えたCBN基競縞材料を得るべく研究を行なった結果
、CBN基焼続材料を、重量%で「Ti、Zr、Ta、
およびWの炭化物、窒化物、および炭窒化物、さらにこ
れらの2種以上の固溶体のうちの1種または2種以上(
以下これらを総称して金属炭・窒化物という):10〜
60%、Pd:1〜10%、NiおよびCoのうちの1
種または2種:1〜10%、N:0.5〜10%を含有
し、残りがCBNと不可避不純物からなり、しかもCB
Nが50〜90容量%を占める組成で構成すると、この
結果のCBN基暁結材料は、すぐれた靭性と耐摩耗性と
を兼ね備え、かつ、すぐれた耐熱性および高温強度を備
えたものとなるという知見を得たのである。However, in the former, as mentioned above, the binder phase is metal, so although it has high toughness, it is easily softened at high temperatures. Under such conditions, the abrasion resistance and adhesion resistance are insufficient, and sufficient cutting performance cannot be expected, and it can only be used under conditions where there is little heat generation, that is, where the load is low.
In addition, in the latter case, as the binder phase is composed of a ceramic compound as mentioned above, it has excellent wear resistance and welding resistance, but on the other hand, lack of rutting can be avoided. First, chipping and chipping are likely to occur under cutting conditions in which a large impact force is applied to the cutting edge, such as when milling high-speed steel. Therefore, from the above-mentioned viewpoint, the present inventors conducted research to obtain a CBN-based striation material that has both toughness and wear resistance. Zr, Ta,
and carbides, nitrides, and carbonitrides of W, and one or more solid solutions of two or more of these (
These are collectively referred to as metal carbon/nitrides): 10~
60%, Pd: 1-10%, one of Ni and Co
Contains 1 to 10% of species or 2 species, 0.5 to 10% of N, and the remainder consists of CBN and inevitable impurities.
When composed of a composition in which N accounts for 50 to 90% by volume, the resulting CBN-based deposited material has excellent toughness and wear resistance, as well as excellent heat resistance and high temperature strength. We obtained this knowledge.
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、以下に成分組成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 knowledge, and the reason why the component composition was limited as described above will be explained below.
【a} 金属炭・窒化物
これらの成分には、超高圧高温下で暁綾を促進し、かつ
材料の耐摩耗性および耐熱性を著しく向上させる均等的
作用があるが、その含有量が10%未満では所望の耐摩
耗性および耐熱性を確保することができず、一方60%
を越えて含有させると、材料の鞠性が低下するようにな
り、例えば切削用として使用した場合刃先に欠損が生じ
易くなることから、その含有量を10〜60%と定めた
。[a} Metallic carbon/nitride These components have the uniform effect of promoting aging under ultra-high pressure and high temperature and significantly improving the wear resistance and heat resistance of the material, but if the content is 10 If it is less than 60%, the desired wear resistance and heat resistance cannot be secured;
If the content exceeds 10%, the ballability of the material decreases and, for example, when used for cutting, the cutting edge tends to be damaged, so the content was set at 10% to 60%.
なお、好ましくは20〜40%の含有が望ましい。‘b
} Pd
Pb成分には、焼結促進作用があるほか、材料の靭性、
耐熱性(耐高温酸化性)、および耐溶着性を向上させ、
その結果耐摩耗性、特に耐クレータ摩耗性を向上させる
作用があるが、その含有量が1%未満では前記作用に所
望の効果が得られず「一方10%を越えて含有させると
材料の耐摩耗性、特に逃げ面摩耗性に劣化傾向が現われ
るようになることから、その含有量を1〜10%と定め
た。Note that the content is preferably 20 to 40%. 'b
} Pd In addition to promoting sintering, the Pb component also improves the toughness of the material.
Improves heat resistance (high temperature oxidation resistance) and welding resistance,
As a result, it has the effect of improving wear resistance, especially crater wear resistance, but if its content is less than 1%, the desired effect cannot be obtained; The content was determined to be 1 to 10% because the abrasion properties, especially the flank abrasion properties, tend to deteriorate.
{c’NiおよびCo
NiおよびCo成分にも暁結を促進させ、かつ材料の靭
‘性を向上させる作用があるが、その合有量が1%未満
では所望の籾性を確保することができず、一方10%を
越えて含有させると、材料の耐熱性および耐落着性が劣
化するようになることから、その含有量を1〜10%と
定めた。{c'Ni and Co Ni and Co components also have the effect of promoting grain set and improving the toughness of the material, but if their combined amount is less than 1%, it is difficult to secure the desired grain quality. On the other hand, if the content exceeds 10%, the heat resistance and settling resistance of the material will deteriorate, so the content was set at 1 to 10%.
{dー AIAI成分には、脱酸作用および焼給促進作
用があるほか、Pd、Ni、およびCoとの共存におい
て、結合相としてPd−(Ni、Co)一AI合金を形
成して材料の耐熱性を著しく向上させる作用があるが、
その含有量が0.5%未満では前記作用に所望の効果が
得られず、一方10%を越えて含有させると、耐摩耗性
および轍性が低下するようになることから、その含有量
を0.5〜10%と定めた。{d-AIAI component has a deoxidizing effect and annealing promoting effect, and when coexisting with Pd, Ni, and Co, forms a Pd-(Ni, Co)-AI alloy as a binder phase and improves the material. It has the effect of significantly improving heat resistance, but
If the content is less than 0.5%, the desired effect cannot be obtained, while if the content exceeds 10%, wear resistance and rutting resistance will decrease. It was set at 0.5-10%.
‘eー CBNの容量比
CBN成分は高硬度並びにすぐれた耐熱性を有する成分
であるが、その割合が5筋容量%未満では所望の耐摩耗
性および耐熱性を材料に付与することができず、一方そ
の割合が9筋容量%を越えると、CBN粒子同志の鞍触
割合が多くなりすぎて、材料が腕化するようになるばか
りでなく、暁絹性も劣化し、材料中に微細なポアーが残
存し易くなって耐摩耗性の劣化を招くようになることか
ら、その容積比を50〜9畔容量%と定めた。'e- CBN volume ratio The CBN component is a component that has high hardness and excellent heat resistance, but if its proportion is less than 5% by volume, the desired wear resistance and heat resistance cannot be imparted to the material. On the other hand, if the ratio exceeds 9 muscle volume%, the ratio of CBN particles in contact with each other becomes too high, which not only causes the material to form arms, but also deteriorates the silkiness and causes fine particles to form in the material. Since pores tend to remain and cause deterioration of wear resistance, the volume ratio was set at 50 to 9% by volume.
つぎに、この発明のCBN基焼結材料を実施例により具
体的に説明する。Next, the CBN-based sintered material of the present invention will be specifically explained using examples.
実施例
原料粉末として、平均粒蚤:6山肌を有するCBN粉末
、いずれも1仏のの平均粒径を有するTIC粉末、TI
N粉末、TICN粉末、ZrC粉末、Z州粉末、ZにN
粉末、TaC粉末、TaN粉末、TaCN粉末、WC粉
末、(Ti、W)C粉末、および(Ti、Zr、Ta)
CN粉末からなる金属炭・窒化物粉末、同様にいずれも
結合相形成成分としての0.5山肌の平均粒径を有する
Pd粉末、Ni粉末、Co粉末、および山粉末「 さら
に平均粒径:0.8仏のを有するPd−AI合金(AI
:20%含有)粉末およびNi−AI合金(AI:32
%含有)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、通常の条件でボールミ
ルにて混合した後、2ton′仇の圧力で直径:25側
め×厚さ:1仇舷の寸法を有する円板状圧粉体に成形し
、ついでこれらの圧粉体を超高圧高温発生装置の容器内
に挿入し、圧力:5仇on/の、温度:1200℃、保
持時間:1時間の条件で超高圧凝結することによって、
実質的に、配合組成と同一の成分組成をもった本発明超
高圧競結材料1〜15および比較超高圧健結材料1〜6
をそれぞれ製造した。Examples of raw material powders include CBN powder having an average grain size of 6 mounds, TIC powder having an average particle size of 1 flea, and TI powder.
N powder, TICN powder, ZrC powder, Z state powder, N in Z
powder, TaC powder, TaN powder, TaCN powder, WC powder, (Ti, W)C powder, and (Ti, Zr, Ta)
Metallic carbon/nitride powder consisting of CN powder, Pd powder, Ni powder, Co powder, and mountain powder each having an average particle size of 0.5 grain size as a binder phase forming component. Pd-AI alloy (AI
:20%) powder and Ni-AI alloy (AI:32
% containing) powder is prepared, and each of these raw material powders is
After blending with the composition shown in the table and mixing in a ball mill under normal conditions, it is pressed into a disc-shaped compact with dimensions of diameter: 25 mm x thickness: 1 mm under a pressure of 2 tons. By molding, then inserting these green compacts into a container of an ultra-high pressure and high temperature generator, and coagulating them under ultra-high pressure under the conditions of pressure: 5 on/, temperature: 1200°C, and holding time: 1 hour.
Ultra-high pressure binding materials 1 to 15 of the present invention and comparative ultra-high pressure binding materials 1 to 6 having substantially the same composition as the blended composition
were manufactured respectively.
なお、比較超高圧燐結材料1〜6は、いずれも構成成分
のうちのいずれかの成分(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
いで、この結果得られた本発明超高圧競結材料1〜15
および比較超高圧競結材料1〜6について、耐摩耗性を
評価する目的で、被削材:ナィモニック8帆、切込み:
0.3肋、送り:0.1肋/回、切削速度:50仇′m
inの条件での切削試験(以下切削試験Aという)、並
びに瓢性を評価する目的で、被削材:ダイス鋼(SKD
−11、硬さ:HRC60)、送り:0.1雌、切込み
:0.05、0.1、0.1ふ0.2、0.2ふ0.入
および0.4凧、切削速度:60仇/min、切削油
:なしの条件での断続切削試験(以下切削試験Bという
)を行ない、切削試験Aでは切刃の逃げ面摩耗が0.2
肋に到るまでの切削時間を測定し、また切削試験Bでは
刃先に欠け発生が見られた送りをチェックした。In addition, comparative ultra-high pressure phosphorized materials 1 to 6 all contain one of the constituent components (those marked with * in Table 1).
has a composition outside the scope of this invention. Next, the ultra-high pressure bonded materials 1 to 15 of the present invention obtained as a result
For the purpose of evaluating the wear resistance of Comparative Ultra High Pressure Bonded Materials 1 to 6, work material: Nimonic 8 sail, depth of cut:
0.3 ribs, feed: 0.1 ribs/time, cutting speed: 50'm
In order to conduct a cutting test under conditions of 100° C. (hereinafter referred to as cutting test A) and to evaluate the cutting properties, the workpiece material: die steel (SKD
-11, hardness: HRC60), feed: 0.1 female, depth of cut: 0.05, 0.1, 0.1 f0.2, 0.2 f0. An intermittent cutting test (hereinafter referred to as "cutting test B") was conducted under the conditions of on and 0.4 kites, cutting speed: 60 m/min, and no cutting oil. In cutting test A, flank wear of the cutting edge was 0.2
The cutting time until the ribs were reached was measured, and in cutting test B, the feed rate at which chipping was observed at the cutting edge was checked.
これらの試験結果をピツカース硬さと共に第1表に合せ
て示した。脳船
第1表に示される結果から、本発明超高圧孫結材料1〜
15は、いずれもすぐれた切削性能を有するのに対して
、比較超高圧燐績材料1〜6に見られるように、構成成
分のうちのいずれかの成分含有量がこの発明の範囲から
外れると切削性能が著しく劣化するようになることが明
らかである。These test results are shown in Table 1 along with the Pickers hardness. From the results shown in Table 1 of Brain Ship, it can be seen that the ultra-high-pressure solar cell materials 1 to 1 of the present invention
No. 15 all have excellent cutting performance, but as seen in comparative ultra-high pressure phosphor materials No. 1 to No. 6, when the content of any of the constituent components deviates from the scope of the present invention. It is clear that the cutting performance deteriorates significantly.
Claims (1)
よび炭窒化物、並びにこれらの2種以上の固溶体のうち
の1種または2種以上:10〜60%、Pd:1〜10
%、NiおよびCoのうちの1種または2種:1〜10
%、Al:0.5〜10%を含有し、残りが立方晶窒化
硼素(ただし50〜90容量%含有)および不可避不純
物からなる組成(以上重量%)を有することを特徴とす
る靭性および耐摩耗性を兼ね備えた切削および耐摩耗工
具用立方晶窒化硼素基超高圧焼結材料。1 Carbides, nitrides, and carbonitrides of Ti, Zr, Ta, and W, and one or more solid solutions of two or more of these: 10 to 60%, Pd: 1 to 10
%, one or two of Ni and Co: 1 to 10
%, Al: 0.5 to 10%, and the remainder consists of cubic boron nitride (containing 50 to 90 volume %) and unavoidable impurities (weight %). Cubic boron nitride-based ultra-high pressure sintered material for cutting and wear-resistant tools with abrasion resistance.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP56211466A JPS602379B2 (en) | 1981-12-25 | 1981-12-25 | Cubic boron nitride-based ultra-high pressure sintered material for cutting and wear-resistant tools |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP56211466A JPS602379B2 (en) | 1981-12-25 | 1981-12-25 | Cubic boron nitride-based ultra-high pressure sintered material for cutting and wear-resistant tools |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS58113349A JPS58113349A (en) | 1983-07-06 |
JPS602379B2 true JPS602379B2 (en) | 1985-01-21 |
Family
ID=16606399
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP56211466A Expired JPS602379B2 (en) | 1981-12-25 | 1981-12-25 | Cubic boron nitride-based ultra-high pressure sintered material for cutting and wear-resistant tools |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS602379B2 (en) |
Families Citing this family (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH0621314B2 (en) * | 1985-12-28 | 1994-03-23 | 住友電気工業株式会社 | Sintered body for high hardness tool and manufacturing method thereof |
US5603075A (en) * | 1995-03-03 | 1997-02-11 | Kennametal Inc. | Corrosion resistant cermet wear parts |
Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5377811A (en) * | 1976-12-21 | 1978-07-10 | Sumitomo Electric Ind Ltd | Sintered material for tools of high hardness and its preparation |
JPS5446109A (en) * | 1977-09-20 | 1979-04-11 | Sumitomo Electric Ind Ltd | Hard alloy and its preparation |
JPS568914A (en) * | 1979-07-04 | 1981-01-29 | Toshiba Corp | Low-frequency dispersed type delay line |
-
1981
- 1981-12-25 JP JP56211466A patent/JPS602379B2/en not_active Expired
Patent Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5377811A (en) * | 1976-12-21 | 1978-07-10 | Sumitomo Electric Ind Ltd | Sintered material for tools of high hardness and its preparation |
JPS5446109A (en) * | 1977-09-20 | 1979-04-11 | Sumitomo Electric Ind Ltd | Hard alloy and its preparation |
JPS568914A (en) * | 1979-07-04 | 1981-01-29 | Toshiba Corp | Low-frequency dispersed type delay line |
Also Published As
Publication number | Publication date |
---|---|
JPS58113349A (en) | 1983-07-06 |
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