JPH02236253A - High hardness sintered body for tool - Google Patents

High hardness sintered body for tool

Info

Publication number
JPH02236253A
JPH02236253A JP1056349A JP5634989A JPH02236253A JP H02236253 A JPH02236253 A JP H02236253A JP 1056349 A JP1056349 A JP 1056349A JP 5634989 A JP5634989 A JP 5634989A JP H02236253 A JPH02236253 A JP H02236253A
Authority
JP
Japan
Prior art keywords
sintered body
binder
group
cbn
cutting
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
JP1056349A
Other languages
Japanese (ja)
Other versions
JP2502364B2 (en
Inventor
Tomohiro Fukaya
朋弘 深谷
Tetsuo Nakai
哲男 中井
Mitsuhiro Goto
光宏 後藤
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.)
Sumitomo Electric Industries Ltd
Original Assignee
Sumitomo Electric Industries Ltd
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Filing date
Publication date
Application filed by Sumitomo Electric Industries Ltd filed Critical Sumitomo Electric Industries Ltd
Priority to JP1056349A priority Critical patent/JP2502364B2/en
Publication of JPH02236253A publication Critical patent/JPH02236253A/en
Application granted granted Critical
Publication of JP2502364B2 publication Critical patent/JP2502364B2/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

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  • Cutting Tools, Boring Holders, And Turrets (AREA)
  • Ceramic Products (AREA)
  • Powder Metallurgy (AREA)

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】 〔産業上の利用分野〕 本発明は立方晶窒化硼素(以下cBNという)を用いた
工具用高硬度焼結体の改良に関する。
DETAILED DESCRIPTION OF THE INVENTION [Industrial Application Field] The present invention relates to improvement of a high hardness sintered body for tools using cubic boron nitride (hereinafter referred to as cBN).

〔従来の技術〕[Conventional technology]

cBNはダイヤモンドに次ぐ高硬度物質であり、その焼
結体は種々の切削工具に使用されている。
cBN is a hard substance second only to diamond, and its sintered bodies are used in various cutting tools.

切削工具に適したこの種のcBN焼結体としては、例え
ば、体積%で70%以上のcBN粒子をAlとNi, 
Co, Mn. Fe,  V, Crからなる群から
選択した合金元素の少なくとも1種を含む金属相により
結合したもの(特開昭4 8−1 7 5 0 3号公
報)、体積%で80〜95%のcBN粒子をTiNまた
はZrNおよび^1−Tiまたは八l−Zrの金属間化
合物およびさらに八l, cBN, TiNまたはZr
Nとの反応により形成される耐熱性化合物よりなる結合
相により結合したもの(特開昭58−55111号公報
)、体積%で80〜95%のcBN粒子を周期律表第r
Va,Va族遷移金属の炭化物、窒化物、炭窒化物と^
1, cBN, Cuとの反応により形成される耐熱性
化合物よりなる結合相により結合したもの(特開昭62
−22840号公報)および体積%で80〜95%のc
BN粒子を周期律表第rVa族の炭化物、窒化物、炭窒
化物とAl, cBN, Cu ,鉄族金属との反応に
より形成される耐熱性化合物からなる結合相により結合
した焼結体(特開昭62−984号公報)等が提案され
ている。
This type of cBN sintered body suitable for cutting tools is, for example, made by combining cBN particles of 70% or more by volume with Al and Ni,
Co, Mn. Bonded by a metal phase containing at least one alloying element selected from the group consisting of Fe, V, and Cr (Japanese Unexamined Patent Publication No. 48-17503), cBN of 80 to 95% by volume The particles can be made of intermetallic compounds of TiN or ZrN and ^1-Ti or 81-Zr and also 81, cBN, TiN or Zr.
cBN particles of 80 to 95% by volume are bonded by a binder phase made of a heat-resistant compound formed by reaction with N (Japanese Patent Laid-Open No. 58-55111), and cBN particles of 80 to 95% by volume are
Va, Va group transition metal carbides, nitrides, carbonitrides and ^
1, bonded by a bonding phase made of a heat-resistant compound formed by reaction with cBN and Cu (Japanese Unexamined Patent Application Publication No. 1983-1999)
-22840) and 80 to 95% c by volume%.
A sintered body (particularly JP-A-62-984) and the like have been proposed.

〔発明が解決しようとする課題〕[Problem to be solved by the invention]

しかしながら、上記のような焼結体を切削工具として使
用した場合にも、例えば耐熱合金や鋳鉄を高速切削する
ように刃先が高温となる切削条件では耐摩耗性の低下に
より、その寿命が比較的短いという欠点があった。
However, even when the above-mentioned sintered body is used as a cutting tool, the wear resistance decreases under cutting conditions where the cutting edge becomes hot, such as when cutting heat-resistant alloys or cast iron at high speed, resulting in a relatively short life. It had the disadvantage of being short.

よって、この発明の目的は、上記した従来のcBN焼結
体よりも、刃先が高温となる切削条件での耐摩耗性に優
れ、高速切削を可能とする焼結体を提供することにある
Therefore, an object of the present invention is to provide a sintered body which has better wear resistance under cutting conditions where the cutting edge becomes hot than the conventional cBN sintered body described above, and which enables high-speed cutting.

〔課題を解決するための手段〕[Means to solve the problem]

本発明者らは上記の目的を達成するため鋭意研究した結
果、cBNを70〜95体積%含有し、残部が下記の結
合材よりなる混合粉末を超高圧焼結すれば、従来のcB
N焼結体よりも刃先が高温となる切削条件での耐摩耗性
に優れたcBN焼結体の得られることを見出し本発明に
到達した。
As a result of intensive research by the present inventors to achieve the above object, we found that if a mixed powder containing 70 to 95% by volume of cBN and the balance consisting of the following binder is sintered under ultra-high pressure, it is possible to achieve the conventional cBN.
The present invention was achieved by discovering that it is possible to obtain a cBN sintered body that has better wear resistance under cutting conditions where the cutting edge becomes hotter than a N sintered body.

すなわち、本発明はcBN粉末を70〜95体積%含有
し、残部が結合材粉末からなる混合粉末を超高圧、高温
下で焼結して得られる焼結体であって、前記結合材がA
1およびA1とTiとの化合物からなる群から選択され
る少なくとも1種2〜50重量%(Al換算)W,WC
およびWとTiとの化合物からなる群から選択される少
なくとも1種2〜50重量%(W換算)および残部がT
iNz, TiCz, Ti(C,N)z,  (Ti
,M)Nz,  (Ti,M)Czおよび(Ti, M
) (C, N) zからなる群から選択される少なく
とも1種のTi化合物(ただし、MはTiを除く周期律
表第IVa,Va,VIa族の遷移元素であり、Q<z
<0.45である)よりなり、含有されるTiと周期律
表第IVa,Va,VIa族の遷移金属元素Mとの割合
が原子比でTi:M=67:100〜97:100であ
る工具用高硬度焼結体に関するものである。
That is, the present invention provides a sintered body obtained by sintering a mixed powder containing 70 to 95% by volume of cBN powder and the remainder consisting of binder powder under ultra-high pressure and high temperature, wherein the binder is A.
2 to 50% by weight (in terms of Al) W, WC of at least one selected from the group consisting of compounds of 1 and A1 and Ti
and 2 to 50% by weight (in terms of W) of at least one selected from the group consisting of compounds of W and Ti, and the remainder is T.
iNz, TiCz, Ti(C,N)z, (Ti
, M)Nz, (Ti,M)Cz and (Ti,M
) (C, N) At least one Ti compound selected from the group consisting of z (where M is a transition element in groups IVa, Va, and VIa of the periodic table excluding Ti, and Q<z
<0.45), and the ratio of the contained Ti to the transition metal element M of groups IVa, Va, and VIa of the periodic table is Ti:M = 67:100 to 97:100 in atomic ratio This invention relates to a high hardness sintered body for tools.

本発明のcBN焼結体では、その生成された焼結体中に
cBNの他、TiN, Tic, Ti(C, N),
  (Ti,M)N,  <Ti,M)Cおよび(Ti
, M) (C, N)からなる群から選択した1種以
上のTi化合物、硼化チタン、前記Mの硼化物、硼化ア
ルミニウム、窒化アルミニウム、タングステン化合物な
らびにタングステンの1種以上を含んでいる。
In the cBN sintered body of the present invention, in addition to cBN, TiN, Tic, Ti(C, N),
(Ti,M)N, <Ti,M)C and (Ti
, M) Contains one or more Ti compounds selected from the group consisting of (C, N), titanium boride, the boride of M, aluminum boride, aluminum nitride, a tungsten compound, and tungsten. .

〔作 用〕[For production]

本発明の焼結体が、刃先が高温となる切削条件での耐摩
耗性に優れ高速切削が可能である理由は以下によるもの
と推測することができる。
The reason why the sintered body of the present invention has excellent wear resistance and is capable of high-speed cutting under cutting conditions where the cutting edge becomes high temperature can be presumed to be due to the following reasons.

一般に焼結体の摩耗は、結合相の摩耗およびcBN粒子
の接合部における破壊によりcBN粒子が脱落していく
ことによって進行する。したがって、刃先が高温となる
切削条件での焼結体の耐摩耗性を向上させるには高温下
でcBN粒子同士およびcBN粒子と結合材が強固に接
合していることおよび結合材自体の強度が高いことが必
要である。本発明の焼結体では、結合材中に^l化合物
を存在させることによって、WC−Co超硬合金の液相
焼結のような硬質粒子の結合相への溶解と再析出現象に
類似した現象が生じ、cBN粒子と結合材およびcBN
粒子同士が接合すると共に結合材中のTi化合物が含ま
れる遊離TiやTiを除く周期律表第IVa,Va,V
Ia族遷移金属MおよびTi−Al金属間化合物中のT
iとcBNが高温高圧下での焼結時に反応し、TI82
や前記Mの硼化物を生成し、それによってcBN粒子と
結合材が強固に接合するものと考えられる。すなわち、
本発明の焼結体の結合相中にはTiの炭化物、窒化物、
炭窒化物に加えてTI82、前記Mの硼化物等も含まれ
る。TiB2とか前記Mの硼化物は脆性であり、刃先の
温度が余り高くならない切削条件では有害となる場合も
あるが、刃先温度が高温となる場合は、TIの炭化物、
窒化物、炭窒化物よりも安定であると考えられ結合相の
高温下での強度および接合力が低下せず好ましい。
Generally, abrasion of a sintered body progresses as cBN particles fall off due to abrasion of the binder phase and fracture at the joints of cBN particles. Therefore, in order to improve the wear resistance of a sintered body under cutting conditions where the cutting edge becomes hot, it is necessary to ensure that the cBN particles are firmly bonded to each other and the cBN particles and the binder at high temperatures, and that the strength of the binder itself is It needs to be high. In the sintered body of the present invention, by making the ^l compound exist in the binder, the phenomenon of dissolution and reprecipitation of hard particles in the binder phase is similar to that in liquid phase sintering of WC-Co cemented carbide. phenomenon occurs, cBN particles, binder and cBN
Periodic table IVa, Va, and V excluding free Ti and Ti, where particles are bonded to each other and contain Ti compounds in the binder.
Group Ia transition metal M and T in Ti-Al intermetallic compound
i and cBN react during sintering under high temperature and pressure, resulting in TI82
It is thought that the cBN particles and the binding material are strongly bonded together by forming boride of the above-mentioned M. That is,
The binder phase of the sintered body of the present invention contains Ti carbides, nitrides,
In addition to carbonitride, TI82, the boride of M mentioned above, etc. are also included. Borides such as TiB2 and M mentioned above are brittle and may be harmful under cutting conditions where the temperature of the cutting edge does not become too high, but when the temperature of the cutting edge becomes high, carbides of TI,
It is considered to be more stable than nitrides and carbonitrides, and is preferable because the strength and bonding force of the binder phase at high temperatures do not decrease.

TiNz, TiCz, Ti(C,N)z,  (T
i,M)Nz,  (Ti,M)Czおよび(Ti, 
M) (C, N) zからなる群から選択した1種以
上のTi化合物(但し、MはTiを除く周期律表第IV
a,Va,VTa族の遷移金属元素であり、Q < z
 <0.45)中の遊離TiはcBN結晶と反応し安<
 TiB2を生成し好ましい。上記化学式におけるZ値
はO<Z<0.45が好ましい。0.45以上ではTi
B2の生成量が減少し結合力が低下する。他方、金属T
i(Z=O)では結合材粉末作成時に粉砕が十分にでき
ず焼結性が低下する。上記Tiの窒化物、炭窒化物に周
期律表第IVa,Va,Vla族遷移金属の窒化物、炭
窒化物を固溶または混合すれば、結合材の強度は大きく
なり、Ti化合物のみを結合材として用いた場合よりも
さらに特性が改善される。この結合材中のTi含有量は
、Tiと、周期律表第IVa,Va,VIa族金属元素
Mの割合が原子比でTi:M=6 7 + 10 0〜
97:100となることが必要である。Tiの含有量が
Ti:M=6 7 : 1 0 0未満では、結合材と
cBNとの結合材が低下して好ましくない。他方、上記
原子比がTi:M=9 7 : 1 0 0を越えると
結合材の耐摩耗性ならびに強度が低下する。
TiNz, TiCz, Ti(C,N)z, (T
i,M)Nz, (Ti,M)Cz and (Ti,
M) (C, N) One or more Ti compounds selected from the group consisting of
It is a transition metal element of the a, Va, VTa group, and Q < z
Free Ti in <0.45) reacts with cBN crystals and
It is preferable to produce TiB2. The Z value in the above chemical formula is preferably O<Z<0.45. Above 0.45, Ti
The amount of B2 produced decreases and the binding strength decreases. On the other hand, metal T
In the case of i (Z=O), sufficient pulverization is not possible during the preparation of the binder powder, resulting in a decrease in sinterability. If nitrides and carbonitrides of transition metals from groups IVa, Va, and Vla of the periodic table are dissolved or mixed with the Ti nitrides and carbonitrides mentioned above, the strength of the binder increases, and only Ti compounds are bonded. The properties are further improved than when used as a material. The Ti content in this bonding material is such that the atomic ratio of Ti and M, a metal element of groups IVa, Va, and VIa of the periodic table, is Ti:M=67+100~
It is necessary that the ratio be 97:100. If the Ti content is less than Ti:M=67:100, the bonding agent between the binder and cBN will deteriorate, which is not preferable. On the other hand, if the atomic ratio exceeds Ti:M=97:100, the wear resistance and strength of the binder will decrease.

A1もしくはAl−Ti金属間化合物の結合材中におけ
る含有量は、2〜50重量%(Al換算)とすることが
必要である。A1の含有量が2重量%未渦の場合にはそ
の添加による効果が不充分であり、50重量%を越える
と結合材の硬度が低下する。好ましくは10〜30重量
%がよい。
The content of A1 or Al-Ti intermetallic compound in the binder needs to be 2 to 50% by weight (in terms of Al). When the content of A1 is 2% by weight without swirling, the effect of its addition is insufficient, and when it exceeds 50% by weight, the hardness of the binder decreases. Preferably it is 10 to 30% by weight.

WCもしくはW化合物は特に耐摩耗性を改善するために
添加するものでその結合材中の含有壷は2〜50重量%
(W換算)とする。Wの含有量が2重量%未満では耐摩
耗性を改善することができず、他方50重量%を越える
と、Ti化合物の含脊量が低下し、cBNと結合材との
接合強度が低下し好ましくない。特に上記の化学式にお
けるMとしてWを用いた場合には、結合材の耐摩耗性お
よび強度が改善され良好な特性を示す。
WC or W compound is added especially to improve wear resistance, and its content in the binder is 2 to 50% by weight.
(converted to W). If the W content is less than 2% by weight, the wear resistance cannot be improved, while if it exceeds 50% by weight, the Ti compound content decreases and the bonding strength between cBN and the binder decreases. Undesirable. In particular, when W is used as M in the above chemical formula, the wear resistance and strength of the binder are improved and exhibits good properties.

本発明の焼結体では、上述した結合材よりなる結合相に
よってcBN粒子が結合している。
In the sintered body of the present invention, cBN particles are bonded by a binder phase made of the above-mentioned binder.

cBN粒子の含有量は70〜95体積%が好ましい。7
0体積%未満では焼結体の硬度、特に高温強度が低下す
るので好ましくなく、地方cBN含有量が95体積%を
越えると、焼結体の靭性が低下し好ましくない。
The content of cBN particles is preferably 70 to 95% by volume. 7
If the local cBN content is less than 0% by volume, the hardness of the sintered body, especially high-temperature strength, will decrease, which is undesirable, and if the local cBN content exceeds 95% by volume, the toughness of the sintered body will decrease, which is undesirable.

〔発明の効果〕〔Effect of the invention〕

この発明では、cBNにTi化合物、A1、WC等を含
む結合材を混合し超高圧高温下で焼結して得られ、cB
N粒子を70〜95体積%含有するほか残部の結合材中
には^1成分が2〜50重量%含有され、硼化アルミニ
ウム、窒化アルミニウム等を形成しており、また該結合
材中にはW成分が2〜50重量%含有され、これはWC
1W化合物等として存在し、さらにはTiの炭化物、窒
化物、炭窒化物等が含有されるので、結合材の強度が高
(、cBNと結合材または結合材自体の接合強度が優れ
ている高硬度工具用焼結体を得ることができる。特にこ
の発明の焼結体は高温下における強度に優れているので
耐熱合金や鋳鉄の高速切削等の用途に適する。
In this invention, cBN is obtained by mixing a binder containing a Ti compound, A1, WC, etc. and sintering it under ultra-high pressure and high temperature.
In addition to containing 70 to 95% by volume of N particles, the remaining binder contains 2 to 50% by weight of the ^1 component, forming aluminum boride, aluminum nitride, etc., and the binder also contains The W component is contained in an amount of 2 to 50% by weight, which is WC.
It exists as a 1W compound, etc., and also contains Ti carbides, nitrides, carbonitrides, etc., so the strength of the binder is high (i.e., the bonding strength between cBN and the binder or the binder itself is excellent). A sintered body for hard tools can be obtained. In particular, the sintered body of the present invention has excellent strength at high temperatures and is therefore suitable for applications such as high-speed cutting of heat-resistant alloys and cast iron.

実施例I Tiを含有する窒化物または炭窒化物粉末と、アルミニ
ウム粉末およびWC粉末とを混合し、これを超硬合金製
のポットおよびボールを用いて平均粒度1μm以下の第
1表に示す組成を有する結合材粉末を作成した。これら
の結合材粉末と、粒度3μm以下のcBN粉末とを体積
比で20対80となるように混合し、混合粉末を作成し
た。Mo製の容器にWC−10重量%Co組成の超硬合
金からなる円板を入れた後これらの混合粉末を充填した
。次に、該容器を超高圧、高温装置にいれ、圧力54k
b,1400℃で25分間焼結した。
Example I Ti-containing nitride or carbonitride powder, aluminum powder and WC powder are mixed and mixed using a cemented carbide pot and ball to form the composition shown in Table 1 with an average particle size of 1 μm or less. A binder powder having the following properties was prepared. These binder powders and cBN powder with a particle size of 3 μm or less were mixed at a volume ratio of 20:80 to create a mixed powder. A disk made of cemented carbide having a composition of WC-10 wt % Co was placed in a container made of Mo, and then the mixed powders were filled therein. Next, the container was placed in an ultra-high pressure, high temperature device, and the pressure was 54k.
b. Sintered at 1400°C for 25 minutes.

得られた焼結体のX線回折結果を第2表に示す。全ての
焼結体においてcBNとTiを含む窒化物、炭化物およ
び炭窒化物のピークが観察された。上記の物質以外に、
TiB2、Ti以外の周期律表第1’Va,Va,VI
a族遷移金属Mの硼化物、AlB2,AlNとWの硼化
物、炭化物もしくはWと思われるピークがS忍められた
Table 2 shows the X-ray diffraction results of the obtained sintered body. Peaks of nitrides, carbides, and carbonitrides containing cBN and Ti were observed in all the sintered bodies. In addition to the above substances,
Periodic table 1'Va, Va, VI other than TiB2 and Ti
Peaks that appeared to be borides of group a transition metals M, AlB2, AlN, and W borides, carbides, or W were observed in S.

また第3表にこれら焼結体のビツカース硬度測定結果を
示す。
Further, Table 3 shows the results of measuring the Vickers hardness of these sintered bodies.

次に、これら焼結体を加工し、切削加工用のチップとし
インコロイ90HIncoloy 901)を切削速度
240m/分、切込み0.15mm,送り0 .08 
mm/ revの切削条件で切削した。切削可能であっ
た時間を第3表に示す。なお第1表に示した原子比[T
i :M]はTiと周期律表第rVa.Va,VIa族
遷移金属元素との原子比を示す。
Next, these sintered bodies were processed to make cutting chips using Incoloy 90H Incoloy 901) at a cutting speed of 240 m/min, depth of cut of 0.15 mm, and feed of 0. 08
Cutting was performed under the cutting conditions of mm/rev. Table 3 shows the time during which cutting was possible. Note that the atomic ratio [T
i:M] is Ti and rVa. of the periodic table. The atomic ratio with Va and group VIa transition metal elements is shown.

第2表(続き) 第 表 得た。この結合材粉末の組成は、重量%で、76%(T
io.s Zro.+)(Co.s N0.5)0.3
 − 1 2%Al−12%WCである。なお、結合材
中のTiとWの原子比は88.5対14.5である。こ
の結合材粉末とcBN粉末とを第4表に示すように混合
し混合粉末を作成した。
Table 2 (continued) Table 2 obtained. The composition of this binder powder is 76% (T
io. sZro. +) (Co.s N0.5) 0.3
-12% Al-12% WC. Note that the atomic ratio of Ti and W in the binder is 88.5:14.5. This binder powder and cBN powder were mixed as shown in Table 4 to create a mixed powder.

得られた混合粉末を実施例1と同様にして超高圧焼結し
、焼結体を得た。得られた焼結体のビツカース硬度測定
結果を第4表に示す。
The obtained mixed powder was subjected to ultra-high pressure sintering in the same manner as in Example 1 to obtain a sintered body. Table 4 shows the results of the Vickers hardness measurement of the obtained sintered body.

次にこれらの焼結体を加工し、切削加工用のチップとし
、S K Dll (H.. 60)を切削した。切削
条件は切削速度190m/分、切り込み  / m m
 ,送り0.5mm/rev乾式である。切削可能であ
った時聞を第4表に示す。
Next, these sintered bodies were processed into chips for cutting, and S K Dll (H.. 60) was cut. Cutting conditions: cutting speed 190m/min, depth of cut/mm
, a dry type with a feed rate of 0.5 mm/rev. Table 4 shows the times during which cutting was possible.

実施例2 (T+o. s Wo. 1) (Co. 2 No.
a) O− 3、Al及びWC粉末を混合し、1μm以
下の粒度の結合材粉末を第 表 実施例3 (Tio. s Zro. +) (Co. s No
. s)zのZの値が異なるTi化合物とAl, WC
粉末を混合し、粒度1,im以下の結合材粉末を作製し
た。これらの結合材粉末の組成は重量%で75%(Ti
,. = 2r。. 1)(Co.s No.s)2 
 1 5%Al− 1 0%WCである。
Example 2 (T+os. Wo. 1) (Co. 2 No.
a) Mix O-3, Al and WC powder and add binder powder with a particle size of 1 μm or less as shown in Table Example 3 (Tio. s Zro. +) (Co. s No.
.. s) Ti compounds with different values of Z and Al, WC
The powders were mixed to produce a binder powder with a particle size of 1.im or less. The composition of these binder powders is 75% by weight (Ti
、. = 2r. .. 1) (Co.s No.s) 2
15% Al-10% WC.

第5表に、これら結合材のTi化合物のZの値と、Ti
と周期律表第IVa,Va,VIa族遷移金属元素との
原子比[Ti: MEを示す。
Table 5 shows the Z value of the Ti compound of these binders and the Ti
The atomic ratio [Ti:ME] of the transition metal elements of groups IVa, Va, and VIa of the periodic table is shown.

これらの結合材粉末と、粒度3Frn以下のcBN粉末
とを容最比25対75の割合で混合し混合粉末を得た。
These binder powders and cBN powder having a particle size of 3 Frn or less were mixed at a volume ratio of 25:75 to obtain a mixed powder.

これらの混合粉末をMo製の容器にいれ超高圧焼結した
。なお、焼結は、50Kbおよび1,350℃に30分
間維持することにより行った。
These mixed powders were placed in a container made of Mo and sintered under ultra-high pressure. Note that sintering was performed by maintaining the temperature at 50 Kb and 1,350° C. for 30 minutes.

これらの焼結体のビツカース硬度測定結果を第6表に示
す。
Table 6 shows the results of the Vickers hardness measurements of these sintered bodies.

次にこれらの焼結体を加工し、切削加工用のチップとし
、レーネ4 1 (Rene 41一商品名一ニッケル
基スーパーアロイ)を切削した。切削条件は、切削速度
:180m/分、切込み:0.12mm,送り: 0 
.1mm/ rev ,乾式である。
Next, these sintered bodies were processed into chips for cutting, and Rene 41 (trade name: nickel-based superalloy) was cut. The cutting conditions were: cutting speed: 180 m/min, depth of cut: 0.12 mm, feed: 0.
.. 1mm/rev, dry method.

切削可能であった時間を第6表に示す。Table 6 shows the time during which cutting was possible.

Claims (3)

【特許請求の範囲】[Claims] (1) 立方晶型窒化磯素粉末を70〜95体積%含有
し、残部が結合材粉末からなる混合粉末を超高圧、高温
下で焼結して得られる焼結体であつて、前記結合材がA
lおよびAlとTiとの化合物からなる群から選択され
る少なくとも1種2〜50重量%(Al換算)、W,W
CおよびWとTiとの化合物からなる群から選択される
少なくとも1種2〜50重量%(W換算)および残部が
TiNz,TiCz,Ti(C,N)Z,(Ti,M)
Nz,(Ti,M)Czおよび(Ti,M)(C,N)
zからなる群から選択される少なくとも1種のTi化合
物(ただし、MはTiを除く周期律表第IVa,Va,V
Ia族の遷移元素であり、0<z<0.45である)よ
りなり、含有されるTiと周期律表第IVa,Va,VIa
族の遷移金属元素Mとの割合が原子比でTi:M=67
:100〜97:100である工具用高硬度焼結体。
(1) A sintered body obtained by sintering a mixed powder containing 70 to 95% by volume of cubic silicon nitride powder and the remainder consisting of binder powder under ultra-high pressure and high temperature, wherein the Material is A
2 to 50% by weight (in terms of Al) of at least one selected from the group consisting of compounds of Al and Ti, W, W
2 to 50% by weight (in terms of W) of at least one selected from the group consisting of compounds of C and W and Ti, and the remainder is TiNz, TiCz, Ti(C,N)Z, (Ti,M)
Nz, (Ti,M)Cz and (Ti,M)(C,N)
At least one Ti compound selected from the group consisting of
It is a transition element of Group Ia, 0<z<0.45), and contains Ti and elements of the periodic table IVa, Va, and VIa.
The ratio of transition metal element M in the group is Ti:M=67 in atomic ratio
:100-97:100 High hardness sintered body for tools.
(2) 前記焼結体が、立方晶窒化硼素の他に、TiN
,TiC,Ti(C,N),(Ti,M)N,(Ti,
M)Cおよび(Ti,M)(C,N)からなる群から選
択される少なくとも1種のTi化合物、硼化チタン、前
記Mの硼化物、硼化アルミニウム、窒化アルミニウム、
W化合物およびWの少なくとも1種を含む請求項(1)
に記載の工具用高硬度焼結体。
(2) The sintered body contains TiN in addition to cubic boron nitride.
, TiC, Ti(C,N), (Ti,M)N, (Ti,
M) at least one Ti compound selected from the group consisting of C and (Ti,M)(C,N), titanium boride, the boride of M, aluminum boride, aluminum nitride,
Claim (1) containing at least one type of W compound and W
High hardness sintered body for tools described in .
(3) Mがタングステンである請求項(1)または(
2)に記載の工具用高硬度焼結体。
(3) Claim (1) or (
2) High hardness sintered body for tools.
JP1056349A 1989-03-10 1989-03-10 High hardness sintered body for tools Expired - Fee Related JP2502364B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP1056349A JP2502364B2 (en) 1989-03-10 1989-03-10 High hardness sintered body for tools

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP1056349A JP2502364B2 (en) 1989-03-10 1989-03-10 High hardness sintered body for tools

Publications (2)

Publication Number Publication Date
JPH02236253A true JPH02236253A (en) 1990-09-19
JP2502364B2 JP2502364B2 (en) 1996-05-29

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ID=13024754

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JP2007169107A (en) * 2005-12-22 2007-07-05 Tungaloy Corp Cubic bn ultra-high pressure sintered compact and its producing method
WO2016084929A1 (en) * 2014-11-27 2016-06-02 三菱マテリアル株式会社 Sintered object based on cubic boron nitride, and cutting tool constituted of sintered object based on cubic boron nitride
JP2016108232A (en) * 2014-11-27 2016-06-20 三菱マテリアル株式会社 Cubic boron nitride-based sintered body, and cutting tool made of cubic boron nitride-based sintered body
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Cited By (7)

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Publication number Priority date Publication date Assignee Title
JP2004160637A (en) * 2002-06-26 2004-06-10 General Electric Co <Ge> Sintered compact used for machining of chemically reactive materials
JP2007169107A (en) * 2005-12-22 2007-07-05 Tungaloy Corp Cubic bn ultra-high pressure sintered compact and its producing method
WO2016084929A1 (en) * 2014-11-27 2016-06-02 三菱マテリアル株式会社 Sintered object based on cubic boron nitride, and cutting tool constituted of sintered object based on cubic boron nitride
JP2016108232A (en) * 2014-11-27 2016-06-20 三菱マテリアル株式会社 Cubic boron nitride-based sintered body, and cutting tool made of cubic boron nitride-based sintered body
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