JPS6033336A - Crystal boron nitride sintered body and preparation thereof - Google Patents

Crystal boron nitride sintered body and preparation thereof

Info

Publication number
JPS6033336A
JPS6033336A JP58142883A JP14288383A JPS6033336A JP S6033336 A JPS6033336 A JP S6033336A JP 58142883 A JP58142883 A JP 58142883A JP 14288383 A JP14288383 A JP 14288383A JP S6033336 A JPS6033336 A JP S6033336A
Authority
JP
Japan
Prior art keywords
sintered body
powder
cbn
liquid phase
binder
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
JP58142883A
Other languages
Japanese (ja)
Other versions
JPS6311414B2 (en
Inventor
Ayanori Okuzumi
奥住 文徳
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.)
Asahi Diamond Industrial Co Ltd
Original Assignee
Asahi Diamond Industrial 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 Asahi Diamond Industrial Co Ltd filed Critical Asahi Diamond Industrial Co Ltd
Priority to JP58142883A priority Critical patent/JPS6033336A/en
Publication of JPS6033336A publication Critical patent/JPS6033336A/en
Publication of JPS6311414B2 publication Critical patent/JPS6311414B2/ja
Granted legal-status Critical Current

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  • Powder Metallurgy (AREA)

Abstract

PURPOSE:To inexpensively prepare a CBN sintered body having an arbitrary dimension and configuration, by dispersing CBN fine particles having a specific volumetric ratio range in a bonding material obtained by alloying a hard heat resistant inorg. compound and a metal according to a liquid phase sintering process. CONSTITUTION:A fine powder comprising a hard heat resistant inorg. compound (e.g., TiN, WC or AlN), a powder comprising a metal alone (e.g., Ni, Co or Ti) and a CBN powder in a volumetric ratio of 60-40% are mixed. In the next step, this powdery mixture is charged in a mold and pressed to 0.3-3kb under vacuum or in an inert atmosohere and heated to 1,200- 1,600 deg.C to obtain a sintered body. The press heating equipment in this case is a so called hot press apparatus and the sintered body with an extremely large dimension can be obtained by small scale equipment as compared with an ultra-high pressure apparatus and operation is also simple. The above mentioned materials of the bonding material are used in forming a CBN sintered body satisfying requirements without necessitating ultra-high pressure but it is necessary to properly select a combination of various materials and a compounding ratio and a sintering treatment condition such as pressure or a temp. This fact shows possibility such that various CBN sintered bodies having different characteristics can be manufactured according to use purpose.

Description

【発明の詳細な説明】 立方晶窒化硼素はまたOBNとも称し、超高圧高温技術
により製造した粉末が供給される。砥粒として硬さはダ
イヤモンドに次ぎ、熱的安定性はダイヤモンドよシもす
ぐれ、また鉄と反応し難い特長によシ、ダイヤモンドで
は及ばない鋼の研削加工などに賞月される。
DETAILED DESCRIPTION OF THE INVENTION Cubic boron nitride, also referred to as OBN, is supplied as a powder produced by ultra-high pressure and high temperature technology. As an abrasive grain, it is second only to diamond in hardness, has better thermal stability than diamond, and because it does not easily react with iron, it is prized for applications such as grinding of steel, which diamond cannot match.

またOBN焼結体なるものが知られ、切削工具材料、耐
摩耗性側斜としての用途がある。一般に厚さ0.り〜1
3 tmのOBN焼結体に超硬合金の裏打を施して合計
厚さ数量の小板状の素材として供給される。焼結体は従
来はOBN粉末と結合材との混合粉末をグ0〜60 K
A (キロバール)の超高圧と/、2θO〜!100℃
の高温すなわちCBNの安定領域内で処理する方法で製
造されている。超高圧高温処理を要するため昆産が困難
で製造費が高く、また焼結晶の寸法形状にも制約が大き
い。
Also, OBN sintered bodies are known and are used as cutting tool materials and wear-resistant side slopes. Generally the thickness is 0. Ri~1
3 tm OBN sintered body with cemented carbide backing and supplied as platelet material in total thickness quantities. Conventionally, the sintered body is a mixed powder of OBN powder and a binder at a temperature of 0 to 60K.
Ultra-high pressure of A (kilobar) and /, 2θO~! 100℃
It is manufactured using a method of processing at high temperatures, that is, within the stability region of CBN. Because it requires ultra-high pressure and high temperature treatment, it is difficult to produce and expensive to produce, and there are also significant restrictions on the size and shape of the fired crystals.

本発明は任意の寸法形状のCBN焼結体を安価に製造す
ることを目的とするもので、本発明は超高圧を要せずθ
3〜J xbすなわち通常の粉体成形機の圧力範囲内で
実用に耐えるCBN焼結体を製造する方法を完成した。
The purpose of the present invention is to manufacture CBN sintered bodies of arbitrary dimensions and shapes at low cost.
3-J xb, that is, a method for producing a CBN sintered body that can be used in practical use within the pressure range of a normal powder compacting machine has been completed.

これを可能にした要点は結合材にある。結合材は容積比
でl/、0〜60%を配するが、材料は硬質で耐熱性の
無機化合物と単体金属との混合で、焼結過程の温度圧力
下で互に反応して比較的低融点の液相を発生すること、
および該液相がCBNをよく濡らす性質を有することを
特徴とする。
The key to making this possible is the binding material. The binder has a volume ratio of l/, 0 to 60%, and the material is a mixture of a hard, heat-resistant inorganic compound and a single metal, which react with each other under the temperature and pressure of the sintering process and are relatively stable. generating a low melting point liquid phase;
Also, the liquid phase has a property of wetting CBN well.

液相がCBNを個らすことはCBN粒の表面における一
種の化学反応を意味し、これにより CBN粒と結合材
特にその液相成分とは強く接着する。また液相は反応に
よシ発生したものであるから、結合拐の残留同相成分を
もよく溢らすので、結合材自体も液相焼結による合金化
によって強められる。
The presence of CBN in the liquid phase means a kind of chemical reaction on the surface of the CBN grains, which causes strong adhesion between the CBN grains and the binder, especially the liquid phase component. Furthermore, since the liquid phase is generated by a reaction, it easily overflows the remaining in-phase components of the bond, so that the bond material itself is strengthened by alloying by liquid phase sintering.

すなわちOBN粒子は強固な結合材を中介として互に強
く結合される。さらに液相は細粒間のを隙に浸透してこ
れを満すためOBNおよび結合材の各粒子はその全表面
で結合されて強靭な焼結体を形成し、気胞が残存して強
度を損ねるなどのおそれがない。
That is, the OBN particles are strongly bonded to each other with a strong binder interposed therebetween. Furthermore, since the liquid phase penetrates into the gaps between the fine particles and fills them, each particle of OBN and binder is bonded on its entire surface to form a strong sintered body, and the air cells remain to increase the strength. There is no risk of damage.

硬質耐熱性無機化合物は窒化チタニウムTiN 。The hard heat-resistant inorganic compound is titanium nitride (TiN).

炭化チタニウムTiO,窒炭化チタニウムTBh+、c
);硼化チタニウムTiB2、酸化チタニウムTio、
 、炭化タ:/ゲステンWc、窒化アルミニウムA7N
 、酸化アルミニウムA/、 O,などから選び、また
単体金属(・ヨ二゛ノクルIJ4.コバル) CO,チ
タニウムTi、シリコンSα などが有用である。
Titanium carbide TiO, titanium nitride carbide TBh+, c
); titanium boride TiB2, titanium oxide Tio,
, carbide ta:/gesten Wc, aluminum nitride A7N
, aluminum oxide A/, O, etc., and simple metals (IJ4, CO, titanium Ti, silicon Sα, etc.) are useful.

これ等無機化合物の1種またはコ種以上と、単体金篇の
1種または2種以上との、いずれも微粉末をOBN粉末
と混合して成形屋に装填し、真空または不活性雰囲気中
で03〜3 KAに加圧し、/:100〜ノ8θO℃に
加熱することによシ焼結を完了する。
A fine powder of one or more of these inorganic compounds and one or more of the single gold particles is mixed with OBN powder and loaded into a molding shop, and then placed in a vacuum or inert atmosphere. Sintering is completed by applying pressure to 03-3 KA and heating to 100-8θO°C.

加圧、加熱設備はいわゆるポットプレス装置で、超高圧
装置よシも小規模の設備ではるかに大寸法の焼結体を製
造することができ、操作も簡単であSc 焼結体は切削工具ないし耐摩耗部品の材料とするため、
摩耗に抗する硬さと、破壊を防ぐ靭性と、これ等の機械
的特性を高温まで保つ耐熱性とが要求される。上述の結
合材相打は超高圧を要することなくこの要求を充す(3
BN焼結体を作るが、各種側斜の組合せと配合比、およ
び圧力、温度などの焼結処理条件を適切に選ばなければ
ならないことはもちるんである。このことはまた、使用
目的にしたがって特性を異にする種々のOBN焼結体を
製作する可能性を示唆する。
The pressurizing and heating equipment is a so-called pot press equipment, which can produce sintered bodies of much larger size with small-scale equipment than ultra-high pressure equipment, and is easy to operate. or as a material for wear-resistant parts,
Hardness to resist wear, toughness to prevent fracture, and heat resistance to maintain these mechanical properties up to high temperatures are required. The above-mentioned mutual bonding of binders satisfies this requirement without requiring ultra-high pressure (3
In order to produce a BN sintered body, it is necessary to appropriately select the combination of various side slopes, the compounding ratio, and the sintering conditions such as pressure and temperature. This also suggests the possibility of producing various OBN sintered bodies with different properties depending on the purpose of use.

なお超硬合金の裏打を有するOBN焼結体を製造するに
は、上述の製法において成形型にCBNを含む混合粉体
の所定銀を装填した上に更に超hi合金材料のWCとC
Oとの混合粉体を装填してホットプレスすれば同時に1
体に焼結して2層の焼結体を得るのである。
In order to manufacture an OBN sintered body having a cemented carbide backing, in the above-mentioned manufacturing method, a predetermined amount of silver in a mixed powder containing CBN is loaded into the mold, and then WC and C of super-hi alloy materials are loaded.
If the mixed powder with O is loaded and hot pressed, 1
A two-layer sintered body is obtained by sintering it into a body.

実施例1 表7の組成の微粉末を混合し、黒鉛型に充填して真空ホ
ットプレス装置に装入し、/ KAの圧力を保って徐々
に昇温し13σθ℃の焼結温度に至って60分間保持、
加圧のまま室温まで降温した後除圧して試料を取出した
。得られた焼結体は結合材の基地中に容積比お%のCB
N粒子が分散する緻密な複合焼結合金組織を示し、抗折
力は大略to lr、g/cl、引掻き試験による硬さ
は1.20種超硬合金をはるかに凌烏する。このOBN
焼結体は耐摩耗材料として優れている。
Example 1 Fine powder having the composition shown in Table 7 was mixed, filled into a graphite mold, placed in a vacuum hot press device, and gradually heated while maintaining a pressure of /KA until a sintering temperature of 13σθ°C was reached at 60°C. Hold for minutes,
After cooling to room temperature while keeping the pressure applied, the pressure was removed and the sample was taken out. The obtained sintered body has a volume ratio of CB in the base of the binder.
It exhibits a dense composite sintered alloy structure in which N particles are dispersed, the transverse rupture strength is approximately tolr, g/cl, and the hardness by scratch test far exceeds that of the 1.20 class cemented carbide. This OBN
Sintered bodies are excellent as wear-resistant materials.

表 7 表 a 表 3 実施例コ 表コの租成の微粉末混合粉体を、実施例1と同方法で、
/ Kb1300℃で60分間焼結処理した。得られた
焼結体は、抗折力!;Okg/ad、引掻き硬さはに2
0種超硬合金よシはるかに大きい。このOBN焼結体は
切削工具材料として優れている。
Table 7 Table a Table 3 The fine powder mixture of Example C and Table C was prepared in the same manner as in Example 1.
/Kb Sintering treatment was performed at 1300°C for 60 minutes. The obtained sintered body has transverse rupture strength! ;Okg/ad, scratch hardness is 2
It is much larger than Type 0 cemented carbide. This OBN sintered body is excellent as a cutting tool material.

実施例3 表3の組成の微粉末混合粉体を、実施例1と同方法で、
/ Kb/7θθ℃で60分間焼結処理した。得られた
焼結体は抗折力、硬さともに前記実施例1よルも若干劣
るが、耐摩耗材料として超硬合金よシもすぐれている。
Example 3 A fine mixed powder having the composition shown in Table 3 was prepared in the same manner as in Example 1.
/Kb/7θθ°C for 60 minutes. Although the obtained sintered body is slightly inferior to those of Example 1 in terms of transverse rupture strength and hardness, it is also superior to cemented carbide as a wear-resistant material.

Claims (3)

【特許請求の範囲】[Claims] (1)硬質耐熱性無機化合物と、金屑とが、液相焼結に
より合金化した結合材中に、容積比60〜旬%のOBN
微粒を分散させた立方晶窒化硼系焼結体。
(1) A hard heat-resistant inorganic compound and gold scrap are mixed into a binder alloyed by liquid phase sintering, and OBN is added to the binder with a volume ratio of 60 to 10%.
Cubic boron nitride-based sintered body with dispersed fine particles.
(2)結合材の材料はTiN、 TiO、T((N、(
り、Ti馬。 Tioz、 wC,htx 、 h401+の何れか一
種又は二種以上の混合粉体であることを特徴とする特許
請求の範囲第1項記載の立方晶積化硼素焼結体。
(2) The materials of the binder are TiN, TiO, T((N, (
Ri, Ti horse. The cubic crystal laminated boron sintered body according to claim 1, which is a mixed powder of one or more of Tioz, wC, htx, and h401+.
(3)硬質耐熱性無機化合物粉体と、これと反応してO
BNを個らす液相を発生する金屑粉末と、容積比AO〜
Q%のqBN粉末との混合粉体を圧力03〜3Kb(キ
ロバール)、温夏lコθθ〜lざ00℃で焼結すること
を特徴とするCBN焼結体製造法。
(3) Hard heat-resistant inorganic compound powder and O
Gold scrap powder that generates a liquid phase containing BN and a volume ratio of AO~
A method for producing a CBN sintered body, characterized by sintering a mixed powder with Q% of qBN powder at a pressure of 03 to 3 Kb (kilobar) and at a temperature of θθ to 00°C in a warm summer.
JP58142883A 1983-08-04 1983-08-04 Crystal boron nitride sintered body and preparation thereof Granted JPS6033336A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP58142883A JPS6033336A (en) 1983-08-04 1983-08-04 Crystal boron nitride sintered body and preparation thereof

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP58142883A JPS6033336A (en) 1983-08-04 1983-08-04 Crystal boron nitride sintered body and preparation thereof

Publications (2)

Publication Number Publication Date
JPS6033336A true JPS6033336A (en) 1985-02-20
JPS6311414B2 JPS6311414B2 (en) 1988-03-14

Family

ID=15325807

Family Applications (1)

Application Number Title Priority Date Filing Date
JP58142883A Granted JPS6033336A (en) 1983-08-04 1983-08-04 Crystal boron nitride sintered body and preparation thereof

Country Status (1)

Country Link
JP (1) JPS6033336A (en)

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS6184303A (en) * 1984-09-28 1986-04-28 Ishizuka Kenkyusho:Kk Manufacture of composite sintered body
JPH0734157A (en) * 1993-07-15 1995-02-03 Agency Of Ind Science & Technol High strength diamond-metal composite sintered compact and its production
JPH0734156A (en) * 1993-07-15 1995-02-03 Agency Of Ind Science & Technol High strength, high pressure type boron nitride-metal composite sintered body and its production
GB2344358A (en) * 1998-11-20 2000-06-07 Takata Corp Airbag base fabric
CN111945050A (en) * 2020-08-19 2020-11-17 燕山大学 Composite material and preparation method thereof

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH0238870A (en) * 1988-07-28 1990-02-08 Fujitsu Ltd Handler and carrier case for semiconductor device

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5749621A (en) * 1980-09-09 1982-03-23 Hitachi Ltd Preparation of heat-resistant resin
JPS5864329A (en) * 1981-09-28 1983-04-16 ゼネラル・エレクトリツク・カンパニイ Composite body of metal-bonded cubic boron nitride and substrate and manufacture thereof

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5749621A (en) * 1980-09-09 1982-03-23 Hitachi Ltd Preparation of heat-resistant resin
JPS5864329A (en) * 1981-09-28 1983-04-16 ゼネラル・エレクトリツク・カンパニイ Composite body of metal-bonded cubic boron nitride and substrate and manufacture thereof

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS6184303A (en) * 1984-09-28 1986-04-28 Ishizuka Kenkyusho:Kk Manufacture of composite sintered body
JPH0734157A (en) * 1993-07-15 1995-02-03 Agency Of Ind Science & Technol High strength diamond-metal composite sintered compact and its production
JPH0734156A (en) * 1993-07-15 1995-02-03 Agency Of Ind Science & Technol High strength, high pressure type boron nitride-metal composite sintered body and its production
GB2344358A (en) * 1998-11-20 2000-06-07 Takata Corp Airbag base fabric
CN111945050A (en) * 2020-08-19 2020-11-17 燕山大学 Composite material and preparation method thereof

Also Published As

Publication number Publication date
JPS6311414B2 (en) 1988-03-14

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