JPH03243742A - TiB↓2-Co based cemented carbide, cutting tools, and manufacturing method of cemented carbide - Google Patents

TiB↓2-Co based cemented carbide, cutting tools, and manufacturing method of cemented carbide

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Publication number
JPH03243742A
JPH03243742A JP2038728A JP3872890A JPH03243742A JP H03243742 A JPH03243742 A JP H03243742A JP 2038728 A JP2038728 A JP 2038728A JP 3872890 A JP3872890 A JP 3872890A JP H03243742 A JPH03243742 A JP H03243742A
Authority
JP
Japan
Prior art keywords
tib
particles
cemented carbide
sintering
grains
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.)
Pending
Application number
JP2038728A
Other languages
Japanese (ja)
Inventor
Shiko Matsuda
至康 松田
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.)
IHI Corp
Original Assignee
Ishikawajima Harima Heavy Industries Co 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 Ishikawajima Harima Heavy Industries Co Ltd filed Critical Ishikawajima Harima Heavy Industries Co Ltd
Priority to JP2038728A priority Critical patent/JPH03243742A/en
Publication of JPH03243742A publication Critical patent/JPH03243742A/en
Pending legal-status Critical Current

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

Abstract

PURPOSE:To manufacture a TiB2-Co series sintered hard alloy having high density and high deflective strength and having a structure with uniform grain size by bonding many TiB2 grains with a bonding layer contg. a Co simple substance or Co. CONSTITUTION:Grains contg. a Co simple substance or Co are mixed with TiB2 grains, and this mixed grains are subjected to pressure sintering in the temp. range of 1,200 to 1,800 deg.C. At this time, the content of Co is regulated to 2 to 30 vol. to the total volume of the TiB2 grains and the bonding layer. In this way, the TiB2-Co series sintered hard alloy excellent in wear resistance and thermal shock resistance can be obtd. by short time sintering and is useful as the material for cutting tools.

Description

【発明の詳細な説明】 「産業上の利用分野」 この発明は、TiBx粒子を主体とし、Co単体あるい
はCoを含有する結合層によって結合してなるT iB
 、−Co系超硬合金および切削工具と製造方法に関す
るものである。
DETAILED DESCRIPTION OF THE INVENTION "Field of Industrial Application" The present invention is directed to TiB, which is composed mainly of TiBx particles and bound by Co alone or a bonding layer containing Co.
, -Co-based cemented carbide, cutting tool, and manufacturing method.

「従来の技術」 TiB、セラミックは、耐熱性と耐摩耗性および耐酸化
性に優れたセラミックとして知られている。
"Prior Art" TiB and ceramics are known as ceramics with excellent heat resistance, wear resistance, and oxidation resistance.

ところがこのセラミックは、高融点であることから、焼
結性が悪く、高密度な焼結体を得ることが極めて困難な
材料であるといわれている。
However, since this ceramic has a high melting point, it is said to have poor sintering properties, making it extremely difficult to obtain a high-density sintered body.

そこで従来、TiB*セラミックの粒子に助剤および結
合剤とし゛てN i−Z rあるいはNiBの粒子を加
えて混合し、この混合粉末を2000℃で1時間程度常
圧焼結することでTiB*焼結体を製造できたという報
告が以下の文献でなされている。
Conventionally, TiB* ceramic particles were mixed with Ni-Zr or NiB particles as an auxiliary agent and binder, and this mixed powder was sintered under normal pressure at 2000°C for about an hour. The following literature reports that a sintered body could be produced.

“F abrication or T itaniu
m D 1borida Cosp−osites  
  K astuhiro  N ishiyama 
  (Coaposites’ 89  :  Roc
ant  advances  in  J apan
 and  TheU n1ted  S tates
”)。
“Fabrication or T itaniu
m D 1borida Cosp-osites
K astuhiro Nishiyama
(Coaposites' 89: Roc
ant advances in Japan
and TheU n1ted States
”).

「発明が解決しようとする課題」 ところで、前記の方法で製造されたTiB1焼結体の抗
折強度を測定した結果が、前記文献に記載され、その測
定結果は、第1O図に示すようになっている。
"Problem to be Solved by the Invention" By the way, the results of measuring the bending strength of the TiB1 sintered body produced by the above method are described in the above document, and the measurement results are as shown in Figure 1O. It has become.

前記文献によれば、TiBz焼結体の相対密度は100
%近くになっているものと思われるにもかかわらず、抗
折強度は第10図に示すようにバラツキが大きく、デー
タの信頼性に欠け、機械材料、構造材料としての信頼性
に欠けるとともに、抗折強度自体、機械材料あるいは構
造材料として不足している問題がある。
According to the above literature, the relative density of the TiBz sintered body is 100
%, as shown in Figure 10, the bending strength varies widely, and the data is unreliable, making it unreliable as a mechanical or structural material. There is a problem that the bending strength itself is insufficient as a mechanical or structural material.

また、前記T iB を焼結体を製造する際の焼結温度
は2000℃であって極めて高温であり、しかも焼結時
間が1時間と長いために、焼結中にTiB、の結晶粒が
異常粒成長を起こし、組織が不均一になって強度の低下
とバラツキの増加をもたらす問題がある。この異常粒成
長を抑制するjこは、焼結時間を短縮するか、焼結温度
を低くすれば良いのであるが、常圧焼結法の場合、前記
の条件で焼結しなくては、製造できないのが現状である
In addition, the sintering temperature when producing the TiB sintered body is 2000°C, which is an extremely high temperature, and the sintering time is as long as 1 hour. There is a problem in that abnormal grain growth occurs and the structure becomes non-uniform, resulting in a decrease in strength and an increase in variation. This abnormal grain growth can be suppressed by shortening the sintering time or lowering the sintering temperature, but in the case of pressureless sintering, sintering must be performed under the above conditions. The current situation is that it cannot be manufactured.

本発明は前記課題を解決するためになされたもので、高
密度で抗折強度が高く、粒径の均一な組織を有し、特性
のバラツキが少ないので機械材料、構造材料としての信
頼性が高いとともに、耐熱性および耐摩耗性に優れ、切
削材料としても好適なT iB 、−Co系超硬合金と
切削工具を提供すること、および超硬合金の製造方法を
提供することを目的とする。
The present invention was made to solve the above problems, and has a structure with high density, high bending strength, and uniform grain size, and has little variation in properties, so it is reliable as a mechanical material or a structural material. The purpose of the present invention is to provide a TiB, -Co-based cemented carbide and a cutting tool that have high heat resistance and wear resistance, and are suitable as cutting materials, and to provide a method for producing the cemented carbide. .

「課題を解決するための手段」 請求項1に記載した発明は前記課題を解決するために、
多数のT iB x粒子をCo単体あるいはCOを含有
する結合層で結合してなるものである。
"Means for solving the problem" In order to solve the problem, the invention stated in claim 1 has the following features:
It is formed by bonding a large number of T iB x particles with Co alone or with a bonding layer containing CO.

請求項2に記載した発明は前記課題を解決するために、
多数のT i B を粒子をCo単体あるいはCOを含
有する結合層で結合してなるTiBt−Co系超硬合金
で切削工具を形成したものである。
In order to solve the above problem, the invention described in claim 2 has the following features:
The cutting tool is made of a TiBt-Co based cemented carbide, which is made by bonding a large number of TiB particles with Co alone or with a bonding layer containing CO.

請求項3に記載した発明は前記課題を解決するために、
多数のTiB、粒子をCo単体あるいはCOを含有する
結合層で結合してなり、T iB 1粒子と結合層の全
体積に対し、Coの含有量を2〜30体積%にしてなる
ものである。
In order to solve the above problem, the invention described in claim 3 has the following features:
It is made by bonding a large number of TiB particles with Co alone or a bonding layer containing CO, and the Co content is 2 to 30% by volume based on the total volume of the TiB particles and the bonding layer. .

請求項4に記載した発明は前記課題を解決するために、
Co単体あるいはCoを含む粒子にT i B を粒子
を混合して得た混合粒子を1200−1800℃の温度
で加圧焼結するものである。
In order to solve the above problem, the invention described in claim 4 has the following features:
Mixed particles obtained by mixing Co alone or Co-containing particles with TiB particles are sintered under pressure at a temperature of 1200 to 1800°C.

「作用」 Co単体あるいはCoを含む結合層は’I’iB*粒子
間において約1200℃で液相になり、その際TiB、
に対して濡れ性に優れるので、従来より低温で焼結した
場合であっても、液層となった結合層がT i B を
粒子の周囲に十分に付き周り、液相焼結により一様な結
合層を形成してT i B を粒子を結合゛する。また
、加圧焼結時にCo単体あるいはCoを含む結合層が液
層となり、その液層にTiB*粒子が囲まれ、T i 
B 1粒子は液層によって静水圧的に等方加圧された場
合と同様な状態となるので、TiB*粒子は焼結中に粒
成長や粒径変化をしている間に液層中で再配列されて均
一に分散し、焼結後に均一な組織を有するT iB 、
−Co系の焼結体が生成される。
"Operation" Co alone or a bonding layer containing Co becomes a liquid phase at about 1200°C between 'I'iB* particles, and at that time, TiB,
Even when sintered at a lower temperature than conventional methods, the bonding layer that has become a liquid layer sufficiently surrounds the particles with T i B , and the liquid phase sintering allows for uniform sintering. A bonding layer is formed to bond the T i B particles. In addition, during pressure sintering, Co alone or a bond layer containing Co becomes a liquid layer, and the TiB* particles are surrounded by the liquid layer.
Since the B1 particles are in the same state as when they are isostatically pressurized by the liquid layer, the TiB* particles grow in the liquid layer during grain growth and change in particle size during sintering. T iB that is rearranged and uniformly distributed and has a uniform structure after sintering,
-Co-based sintered body is produced.

以下に本発明を更に詳細に説明する。The present invention will be explained in more detail below.

第1図は本発明のT iB 、−Co系焼結体の一実施
例の組織を拡大して示し、たちので、第1図において符
号AはTiB*粒子、符号Bは結合層を示し、多数のT
 i B を粒子Aはその周囲を結合層Bで覆われて相
互に結合された状態となっている。前記結合層Bとして
は、Co単体層、Co+Mo層、Co+WC層、Co+
Ni層、あるいは、これらの混合層などから適宜選択す
ることができるが、これらの層に限定されるものではな
く、Coを含む種々の結合層(粘結剤の層)を使用する
ことができる。
FIG. 1 shows an enlarged view of the structure of an example of the TiB, -Co-based sintered body of the present invention. Therefore, in FIG. 1, symbol A indicates TiB* particles, symbol B indicates a bonding layer, many T
i B The particles A are surrounded by a bonding layer B and are bonded to each other. The bonding layer B includes Co single layer, Co+Mo layer, Co+WC layer, Co+
It can be appropriately selected from a Ni layer or a mixed layer thereof, but is not limited to these layers, and various bonding layers (binder layers) containing Co can be used. .

次に前記TiB、−Co系の焼結体の製造方法の一例に
ついて説明する。
Next, an example of a method for manufacturing the TiB, -Co-based sintered body will be described.

前記構造のTiB、−Co系の焼結体を製造するには、
例えば、粒径を揃えたTiBx粉末などのTiB2粒子
とCo粉末などのCo粒子を用意し、次いでこれらを所
定の割合で混合する。これらめ粒子を混合する場合、T
iB、粒子とCo粒子を合わせた全体の体積に対し、C
o含有量が2〜30体積%の範囲になるように混合する
。ここでCo含有量を2体積%より少なくするか30体
積%よりも多くすると、得られるTiBt−Co焼結体
の強度が低下するので好ましくない。また、混合する各
粒子の粒径は、通常の超硬合金を粉末法で製造する場合
と同様にできる限り小さく、かつ、粒径を揃えることが
好ましい。
To produce a TiB, -Co-based sintered body with the above structure,
For example, TiB2 particles such as TiBx powder and Co particles such as Co powder having the same particle size are prepared, and then these are mixed at a predetermined ratio. When mixing these particles, T
iB, for the total volume of particles and Co particles, C
Mix so that the o content is in the range of 2 to 30% by volume. If the Co content is less than 2% by volume or more than 30% by volume, the strength of the TiBt-Co sintered body obtained will decrease, which is not preferable. Further, it is preferable that the particle size of each particle to be mixed is as small as possible and uniform in particle size, as in the case of manufacturing ordinary cemented carbide by a powder method.

次に、前記のように混合した混合粒子を加圧しながら加
熱して焼結する。
Next, the mixed particles mixed as described above are heated and sintered while being pressurized.

第2図は、前記混合粒子を加圧しながら加熱する装置の
一例を示すもので、この例の装置はホットプレス装置の
1種である。lはヒータを示し、このヒータlの内部側
には、押棒2と型材3とスペーサ4と下台5とからなる
プレス装置が設けられ、下台5の上に設置した試料6を
押棒2で加圧しつつヒータ1で所望の温度に加熱できる
ようになっている。なお、加圧加熱装置の全体は真空容
器に封入されていて、この真空容器内部の真空度を1.
3XlO′□’Pa程度に設定できるようになっている
FIG. 2 shows an example of an apparatus for heating the mixed particles while pressurizing them, and the apparatus in this example is a type of hot press apparatus. l indicates a heater, and a press device consisting of a push rod 2, a mold material 3, a spacer 4, and a lower stand 5 is provided inside the heater l, and a sample 6 placed on the lower stand 5 is pressurized with the push rod 2. At the same time, the heater 1 can be used to heat to a desired temperature. The entire pressurizing and heating device is enclosed in a vacuum container, and the degree of vacuum inside this vacuum container is set to 1.
It can be set to about 3XlO'□'Pa.

この例の装置を使用して前記混合粉末を焼結するには、
混合粒子を下台5の上に設置し、全体を真空排気すると
ともに、押棒2で混合粉末を60MPa程度の加圧力で
加圧し、1200〜1800℃に加熱して焼結する。焼
結時間は短い方が好ましいが、十分に焼結するために、
かつ、結晶粒の異常成長を避ける目的で30分程度とす
る。
To sinter the mixed powder using the apparatus of this example,
The mixed particles are placed on the lower stand 5, and the whole is evacuated, and the mixed powder is pressed with a pressure of about 60 MPa using the push rod 2, and heated to 1200 to 1800°C to sinter. It is preferable that the sintering time be short, but in order to achieve sufficient sintering,
In addition, the heating time is set to about 30 minutes in order to avoid abnormal growth of crystal grains.

以上のように焼結することで、T i B x粒子Aよ
りも融点の低い00層が選択的に液層となる。このCo
の液層はTiB*粒子Aに対して濡れ性に優れるので、
coの液層はT i B *粒子Aの周囲に十分に付き
周り、TiB、粒子Aの周囲に−様なC。
By sintering as described above, the 00 layer, which has a melting point lower than that of the T i B x particles A, selectively becomes a liquid layer. This Co
The liquid layer has excellent wettability for TiB* particles A, so
The liquid layer of co sufficiently surrounds TiB*particle A, TiB, and -like C around particle A.

の液層が形成される。そして、T iB 、粒子Aは、
Coの液層に完全に囲まれた状態となり、しかも、全体
が加圧されているので、TiB、粒子Aは外部から静水
圧的に等方加圧された場合と同様の効果を受ける。従っ
て、焼結中にT i B *粒子Aの粒成長や粒径の変
化がなされている間にTiB、粒子Aが再配列され、結
果的に組織が均一化されたTiBt−Co焼結体が得ら
れる。
A liquid layer is formed. And T iB , particle A is
Since they are completely surrounded by the Co liquid layer and are pressurized as a whole, the TiB and particles A receive the same effect as when they are isostatically pressurized from the outside using hydrostatic pressure. Therefore, during sintering, TiB and particles A are rearranged while the grain growth and grain size of TiB*particles A are changed, resulting in a TiBt-Co sintered body with a uniform structure. is obtained.

また、前記のT iB !−Co焼結体にあってはTi
B!粒子Aよりも破壊靭性の高いCoあるいはG。
Also, the aforementioned T iB! -Ti in the Co sintered body
B! Co or G has higher fracture toughness than particle A.

を含む結合層BでTiB、粒子Aを結合しているので、
TiB*単体を焼結したものよりも遥かにクラックの伝
播速度が遅くなり、結果的に破壊靭性が向上する。従っ
て本発明によって得られるTiB。
Since TiB and particles A are bonded in a bonding layer B containing
The crack propagation speed is much slower than when TiB* alone is sintered, resulting in improved fracture toughness. Therefore, TiB obtained according to the present invention.

CO系焼結体は従来のセラミック切削材料(PIOlT
 iN 、 T iC、A l*o s)よりも耐摩耗
性に優れる。
The CO-based sintered body is a conventional ceramic cutting material (PIOIT).
It has better wear resistance than iN, TiC, Al*os).

以上説明したように製造されたT iB 、−Co焼結
体は、抗折強度が約800〜1000MPa、硬度30
00〜3500Hvという優れた機械特性を有し、優れ
た耐摩耗性と耐熱衝撃性を有する。
The TiB, -Co sintered body manufactured as described above has a bending strength of about 800 to 1000 MPa and a hardness of 30
It has excellent mechanical properties of 00 to 3500 Hv, and has excellent abrasion resistance and thermal shock resistance.

従って本発明のT iB *−G o系焼結体を用いて
切削工具、ブレード、シャフトなどを製造することがで
きる。
Therefore, cutting tools, blades, shafts, etc. can be manufactured using the T iB *-G o based sintered body of the present invention.

更に、T jB x −G O系超硬合金の他の応用例
として、PVD法(物理蒸着法)、CVD法(化学気相
蒸着法)を実施することより製造されるNHとして応用
することもできる。この場合は、TiBxCo系の適当
な組成のターゲットを用い、前記の方法で成膜すること
で膜状のT iB !−Co焼結体を得ることができる
Furthermore, as another application example of TjB x -G O-based cemented carbide, it can also be applied as NH produced by carrying out PVD method (physical vapor deposition method) and CVD method (chemical vapor deposition method). can. In this case, by using a TiBxCo target with an appropriate composition and forming a film using the method described above, a film of TiB! -Co sintered body can be obtained.

更にまた、TiB4.sは超伝導性を示すことが知られ
ているので、本発明方法を応用してB量の制御によって
TiB+、sを生成し、超伝導材料を開発する技術にも
発展させることができる。
Furthermore, TiB4. Since s is known to exhibit superconductivity, the method of the present invention can be applied to generate TiB+, s by controlling the amount of B, and can also be developed into a technology for developing superconducting materials.

なお、前記の製造方法では、焼結温度を1200〜18
00℃にすることができるので、従来の方法よりも焼結
温度を下げることができるとともに、焼結時間も従来の
1時間よりも短縮できる。
In addition, in the above manufacturing method, the sintering temperature is 1200 to 18
Since the sintering temperature can be lowered to 00°C, the sintering temperature can be lower than that of conventional methods, and the sintering time can also be shorter than the conventional one hour.

従って得られる焼結体の結晶粒径を微細化することがで
きる。
Therefore, the crystal grain size of the obtained sintered body can be made finer.

ところで、前記の例では、焼結手段としてホットプレス
法を用いているが、焼結温度の低下と焼結時間の低下を
実現するためには、通電焼結法、HIPなどの焼結法を
適用しても良い。
By the way, in the above example, a hot press method is used as the sintering method, but in order to reduce the sintering temperature and sintering time, a sintering method such as electric sintering or HIP may be used. May be applied.

「実施例」 T i B x粉末とCO粉末を混合してなる混合粉末
を形成し、この混合粉末を第2図に示す加圧加熱装置に
挿入し、真空度をI 、3 X 10−’Pa、加圧力
を60MPa、焼結温度を1200〜1800℃、焼結
時間を30分、昇温速度を15℃/分にそれぞれ設定し
、Co含有量を以下に示す第1表に示すように設定して
ホットプレスを行いT iB 。
"Example" A mixed powder is formed by mixing T i B x powder and CO powder, and this mixed powder is inserted into the pressure heating device shown in FIG. 2, and the degree of vacuum is set to I, 3 x 10-'. The pressure was set at 60 MPa, the sintering temperature was set at 1200 to 1800°C, the sintering time was set at 30 minutes, and the temperature increase rate was set at 15°C/min, and the Co content was determined as shown in Table 1 below. Set and hot press T iB.

−Coo焼結体製造した。-Coo sintered body was manufactured.

以上のように製造されたTiB1Co焼結体と従来方法
によるT i B *焼結体についてビッカース硬さの
測定結果とCo含有量の関係を第3図に示し、同焼結体
の結晶粒径および抗折強度の測定結果とCo含有量との
関係を第4図に示した。
Figure 3 shows the relationship between the Vickers hardness measurement results and the Co content for the TiB1Co sintered body produced as described above and the TiB* sintered body produced by the conventional method. FIG. 4 shows the relationship between the measurement results of the bending strength and the Co content.

第3図と第4図に示す結果から、Co含有量の下限は2
体積%が好適であり、Co含有量の上限は30体積%が
好適であることが判明した。
From the results shown in Figures 3 and 4, the lower limit of Co content is 2.
It has been found that the upper limit of the Co content is preferably 30% by volume.

また、本発明構成のT iB 、−Coo焼結体、抗折
強度約800〜1000MPa、硬度3000〜350
0Hvという優れた機械特性を発揮することが明らかと
なった。
Moreover, the TiB, -Coo sintered body of the present invention has a bending strength of approximately 800 to 1000 MPa and a hardness of 3000 to 350 MPa.
It has become clear that it exhibits excellent mechanical properties of 0Hv.

更に、第5図ないし第7図に、本発明のTiBz−Co
o焼結体種々の温度のサーマルショックを与えた後の常
温強度を測定した結果を示し、第8図に従来方法で得ら
れたT i B !焼結体に種々の温度のサーマルショ
ックを与えた後に常温強度を測定した結果を示す。
Further, FIGS. 5 to 7 show the TiBz-Co of the present invention.
Figure 8 shows the results of measuring the room temperature strength of the sintered body after applying thermal shock at various temperatures. The results of measuring the room temperature strength after applying thermal shock at various temperatures to the sintered body are shown.

これらの結果から、TiBy−Coo焼結体、従来のT
 i B !焼結体に比較して高温強度も優れているこ
とが明らかになった。
From these results, TiBy-Coo sintered body, conventional T
iB! It has become clear that the high-temperature strength is also superior to that of sintered bodies.

第9図は、従来のT iB を焼結体と本発明のTiB
1Co焼結体およびその他各種材料から工具を形成し、
各工具によって切削加工を行った場合の切削試験結果を
記載したものである。第9図において○印とム印とΔ印
で示すデータが、本発明のTiBt−Co焼結体製の工
具の切削試験結果を示す。
FIG. 9 shows a conventional TiB sintered body and a TiB of the present invention.
Forming tools from 1Co sintered bodies and various other materials,
The cutting test results are shown when cutting is performed using each tool. In FIG. 9, the data indicated by ◯, square, and ∆ indicate the cutting test results of the tool made of the TiBt-Co sintered body of the present invention.

第9図に示す結果から、本発明のT iB x−G o
焼結体は優秀な耐摩耗性と耐熱衝撃性を有し、切削工具
用として優秀な性能を発揮することが明らかとなった。
From the results shown in FIG. 9, it can be seen that T iB x-G o of the present invention
It has been revealed that the sintered body has excellent wear resistance and thermal shock resistance, and exhibits excellent performance as a cutting tool.

「発明の効果」 以上説明したように請求項1に記載した発明によれば、
抗折強度と硬度が高く、優れた機械特性を有し、しかも
、耐摩耗性と耐熱衝撃性に優れたT iB *−Co系
超超硬合金提供することができる。
"Effect of the invention" As explained above, according to the invention stated in claim 1,
It is possible to provide a TiB*-Co-based cemented carbide having high transverse strength and hardness, excellent mechanical properties, and excellent wear resistance and thermal shock resistance.

請求項2に記載した発明によれば、抗折強度と硬度が高
く、優れた機械特性を有し、しかも、耐摩耗性と耐熱衝
撃性に優れた優秀な切削工具を提供することができる。
According to the invention described in claim 2, it is possible to provide an excellent cutting tool that has high bending strength and hardness, has excellent mechanical properties, and has excellent wear resistance and thermal shock resistance.

請求項3に記載した発明によれば、Co含有量を特別の
範囲に限定しているので、抗折強度と硬度が更に高く、
特別に優秀な耐摩耗性と耐熱衝撃性とを有するT iB
 、−G o系超硬合金を提供することができる。
According to the invention described in claim 3, since the Co content is limited to a specific range, the bending strength and hardness are even higher,
T iB with exceptional abrasion resistance and thermal shock resistance
, -G o-based cemented carbide can be provided.

請求項4に記載した発明によれば、焼結温度を従来より
低くすることができZとともに、焼結時間を従来よりも
短縮でき、焼結時の結晶粒の異常成長を抑制できるので
、微細かつ均一な結晶粒であって、高強度かつ優れた耐
摩耗性と耐熱衝撃性のT iB !−CO系超硬合金を
製造することができる。
According to the invention described in claim 4, the sintering temperature can be lowered than before, and the sintering time can be shortened than before, and abnormal growth of crystal grains during sintering can be suppressed, so that fine grains can be reduced. T iB has uniform crystal grains, high strength, and excellent wear resistance and thermal shock resistance! -CO based cemented carbide can be manufactured.

また、従来よりも焼結温度を低くできるので、焼結装置
に対する負担が少ないとともに、焼結時間を短縮できる
ので、製造時間も短縮することができる。
Further, since the sintering temperature can be lowered than in the past, there is less burden on the sintering equipment, and the sintering time can be shortened, so the manufacturing time can also be shortened.

【図面の簡単な説明】 第1図は本発明のT iB !合金の組織の拡大図、第
2図は本発明方法を実施する場合に用いる装置の一例を
示す断面図、第3図は本発明のT iB t−Co系超
超硬合金おけるCo含有量とビッカース硬さの関係を示
す線図、第4図は超硬合金における結晶粒径および抗折
強度とCo含有量の関係を示す線図、第5図はCoを2
%含有するT iB 、−C。 系超硬合金における加熱温度と常温強度の関係を示す線
図、第6図はCoを6%含有するT iB 、−C0系
超硬合金における加熱温度と常温強度の関係を示す線図
、第7図はCoを10%含有するTiBt−Co系超硬
合金における加熱温度と常温強度の関係を示す線図、第
8図は従来のT r B y焼結体における加熱温度と
常温強度の関係を示す線図、第9図は本発明合金および
その他各成分の合金およびセラミックスにおける切削試
験結果を示す線図、第10図は各種の粘結剤を添加した
従来のT iB 。 焼結体の強度を示す線図である。 A・・・TiBy粒子、B・・・結合層、■・・・ヒー
タ、2・・・押棒、3・・型材、4・・・スペーサ、5
・・・下台、6・・試料。
[Brief Description of the Drawings] Figure 1 shows the T iB! of the present invention. Figure 2 is an enlarged view of the structure of the alloy, Figure 2 is a cross-sectional view showing an example of the apparatus used to carry out the method of the present invention, and Figure 3 is a diagram showing the Co content and Figure 4 is a diagram showing the relationship between Vickers hardness, Figure 4 is a diagram showing the relationship between grain size and bending strength, and Co content in cemented carbide, and Figure 5 is a diagram showing the relationship between Co content in cemented carbide.
% containing T iB , -C. Figure 6 is a diagram showing the relationship between heating temperature and room temperature strength in T iB -C0 series cemented carbide containing 6% Co. Figure 7 is a diagram showing the relationship between heating temperature and room temperature strength in a TiBt-Co cemented carbide containing 10% Co, and Figure 8 is a diagram showing the relationship between heating temperature and room temperature strength in a conventional T r By sintered body. FIG. 9 is a diagram showing cutting test results for the alloy of the present invention and other alloys and ceramics, and FIG. 10 is a diagram showing conventional T iB to which various binders are added. FIG. 3 is a diagram showing the strength of a sintered body. A: TiBy particles, B: bonding layer, ■: heater, 2: push rod, 3: mold material, 4: spacer, 5
...lower stand, 6...sample.

Claims (4)

【特許請求の範囲】[Claims] (1)多数のTiB_2粒子をCo単体あるいはCoを
含有する結合層で結合してなることを特徴とするTiB
_2−Co系超硬合金。
(1) TiB characterized by being formed by bonding a large number of TiB_2 particles with Co alone or a bonding layer containing Co.
_2-Co-based cemented carbide.
(2)多数のTiB_2粒子をCo単体あるいはCoを
含有する結合層で結合してなるTiB_2−Co系超硬
合金からなる切削工具。
(2) A cutting tool made of TiB_2-Co based cemented carbide, which is made by bonding a large number of TiB_2 particles with Co alone or a bonding layer containing Co.
(3)多数のTiB_2粒子をCo単体あるいはCoを
含有する結合層で結合してなり、TiB_2粒子と結合
層の全体積に対し、Coの含有量を2〜30体積%にし
てなることを特徴とするTiB_2−Co系超硬合金。
(3) A large number of TiB_2 particles are bonded by Co alone or a bonding layer containing Co, and the Co content is 2 to 30% by volume based on the total volume of the TiB_2 particles and bonding layer. TiB_2-Co based cemented carbide.
(4)Co単体あるいはCoを含む粒子にTiB_2粒
子を混合して得た混合粒子を1200〜1800℃の温
度で加圧焼結することを特徴とするTiB_2−Co系
超硬合金の製造方法。
(4) A method for producing a TiB_2-Co cemented carbide, which comprises pressurizing and sintering mixed particles obtained by mixing TiB_2 particles with Co alone or particles containing Co at a temperature of 1200 to 1800°C.
JP2038728A 1990-02-20 1990-02-20 TiB↓2-Co based cemented carbide, cutting tools, and manufacturing method of cemented carbide Pending JPH03243742A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP2038728A JPH03243742A (en) 1990-02-20 1990-02-20 TiB↓2-Co based cemented carbide, cutting tools, and manufacturing method of cemented carbide

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP2038728A JPH03243742A (en) 1990-02-20 1990-02-20 TiB↓2-Co based cemented carbide, cutting tools, and manufacturing method of cemented carbide

Publications (1)

Publication Number Publication Date
JPH03243742A true JPH03243742A (en) 1991-10-30

Family

ID=12533390

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2038728A Pending JPH03243742A (en) 1990-02-20 1990-02-20 TiB↓2-Co based cemented carbide, cutting tools, and manufacturing method of cemented carbide

Country Status (1)

Country Link
JP (1) JPH03243742A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2016191116A (en) * 2015-03-31 2016-11-10 日本タングステン株式会社 Rigid composite material and cutting tool and wear resistant member using the same

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2016191116A (en) * 2015-03-31 2016-11-10 日本タングステン株式会社 Rigid composite material and cutting tool and wear resistant member using the same

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