JP3146803B2 - Method for producing cubic boron nitride based ultra-high pressure sintered material with excellent wear resistance - Google Patents

Method for producing cubic boron nitride based ultra-high pressure sintered material with excellent wear resistance

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Publication number
JP3146803B2
JP3146803B2 JP27534793A JP27534793A JP3146803B2 JP 3146803 B2 JP3146803 B2 JP 3146803B2 JP 27534793 A JP27534793 A JP 27534793A JP 27534793 A JP27534793 A JP 27534793A JP 3146803 B2 JP3146803 B2 JP 3146803B2
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JP
Japan
Prior art keywords
powder
boron nitride
cylindrical container
cubic boron
ultra
Prior art date
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Expired - Fee Related
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JP27534793A
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Japanese (ja)
Other versions
JPH07133154A (en
Inventor
文洋 植田
竜一 丹下
逸郎 田嶋
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Mitsubishi Materials Corp
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Mitsubishi Materials Corp
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Publication of JP3146803B2 publication Critical patent/JP3146803B2/en
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Description

【発明の詳細な説明】DETAILED DESCRIPTION OF THE INVENTION

【0001】[0001]

【産業上の利用分野】この発明は、一段と優れた耐摩耗
性を有し、特にこれらの特性が要求される高速切削工具
として用いるのに適した立方晶窒化ほう素(以下CBN
という)基超高圧焼結材料に関するものである。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a cubic boron nitride (hereinafter referred to as "CBN") which has more excellent wear resistance and is particularly suitable for use as a high-speed cutting tool requiring these characteristics.
) Based ultra-high pressure sintering materials.

【0002】[0002]

【従来の技術】従来、例えば特公昭61−43312に
記載されている様に、容量%で(以下%は容量%を示す)
結合相形成成分としてTi、ZrおよびHfの炭化物、窒
化物および炭窒化物のうち1種または2種以上(以下金
属の炭窒化物と言う):10〜60%、同じく結合相形
成成分として酸化アルミニウム(以下Al23で示す)
および酸化ジルコニウムのうち1種または2種:0.1
〜18%を含有し、残りが分散相形成成分としてのCB
Nからなる配合組成を有するCBN基超高圧焼結材料が
知られており、また、これらCBN基超高圧焼結材料
は、表面硬化鋼などの高硬度鋼の切削に切削工具として
用いられる事も知られている。
2. Description of the Related Art Conventionally, as described in, for example, Japanese Patent Publication No. 61-43312, in terms of volume% (% indicates volume%).
One, two or more of carbides, nitrides and carbonitrides of Ti, Zr and Hf (hereinafter referred to as metal carbonitrides): 10 to 60% as a bonding phase forming component, and oxidation as a bonding phase forming component Aluminum (hereinafter indicated as Al 2 O 3 )
And one or two of zirconium oxide: 0.1
CB as a dispersed phase forming component
CBN-based ultra-high pressure sintering materials having a composition of N are known, and these CBN-based ultra-high pressure sintering materials may be used as cutting tools for cutting hardened steel such as surface hardened steel. Are known.

【0003】[0003]

【発明が解決しようとする課題】一方、近年の切削機械
の高性能化は目覚しく、かつ切削加工の省力化とも相ま
って、切削が高速化する傾向にあるが、上記の従来CB
N基超高圧焼結材料で構成された切削工具においては、
これを高速切削に使用すると、摩耗の進行が早く、比較
的短時間で使用寿命に至るのが現状である。
On the other hand, in recent years, the performance of cutting machines has been remarkably improved, and the cutting speed tends to be increased in conjunction with the labor saving of the cutting process.
In cutting tools composed of N-base ultra-high pressure sintered materials,
When this is used for high-speed cutting, wear progresses quickly, and at present, the service life is reached in a relatively short time.

【0004】[0004]

【課題を解決するための手段】 本発明者等は、上記問
題点を解決するために、上記従来CBN基焼結材料に着
目し、これのより一層の耐摩耗性向上を計るべく、研究
を行った結果、原料粉末として、1〜10μmの範囲内
の所定の平均粒径を有するCBN粉末、金属の炭窒化物
粉末およびAl 2 3 粉末、さらにAl(OH) 3 粉末を用
意し、まず前記CBN粉末と前記Al(OH) 3 粉末とを
NH 4 OH溶液の中で撹拌混合した後、乾燥することに
よりAl 2 3 で包まれたAl 2 3 包囲CBN粉末を調整
し、これら原料粉末を配合し、これらの配合粉末を、そ
れぞれWC基超硬合金で内張りされた粉砕ミル内に装入
し、さらに前記配合粉末に対してメチルアルコールを加
えて混合し、混合後、前記ミルの蓋をアルゴン雰囲気中
で開放し、加焼して前記メチルアルコールを蒸発させ、
乾燥し、ついで同じくアルゴン雰囲気内において、別途
用意したTi製円筒型容器の底部に、まず同じく別途用
意したWC基超硬合金製円板を装入し、この円板上に上
記混合粉末を装入し、押し棒で押えて充填し、この充填
混合粉末上にWC基超硬合金製円板を敷置し、つぎにア
ルゴン雰囲気から取りだした後、さらにTi製上蓋をか
ぶせてプレスして前記Ti製円筒型容器内の混合粉末の
厚みを圧縮し、引続いて前記円筒型容器に前記上蓋を溶
接して、これを密封し、このように上記混合粉末を充填
して密封した円筒型容器を超高圧超高温発生装置に装入
し、最高付加圧力:4〜5GPa、温度範囲:1300〜
1500℃の条件で保持した後、冷却についで圧力解放
を行うことで、CBN基焼結材料において結合相を形成
する金属の炭窒化物とCBN粒子との間にAl23層を
介在、すなわちCBN粒子の表面に連続的または断続的
にAl2O3包囲層を形成すると、前記Al23包囲層
は、CBN粒子および上記結合相のいずれに対しても優
れた密着性を持つことから、これを切削工具として用
い、高速切削を行ってもCBN粒子の脱落が著しく抑制
される様になることから、一段と優れた耐摩耗性を発揮
し、長期に亘って優れた切削性能を示すという研究結果
を得たのである。
Means for Solving the Problems In order to solve the above problems, the present inventors have paid attention to the above-mentioned conventional CBN-based sintered material, and have conducted research to further improve the wear resistance thereof. As a result, as a raw material powder, within the range of 1 to 10 μm
Powder having a predetermined average particle size, metal carbonitride
For powder, Al 2 O 3 powder, and Al (OH) 3 powder
First, the CBN powder and the Al (OH) 3 powder
After stirring and mixing in an NH 4 OH solution,
Adjusting the Al 2 O 3 enclosing CBN powder wrapped in more Al 2 O 3
Then, these raw material powders are blended, and these blended powders are
Each is charged into a grinding mill lined with WC-base cemented carbide
And adding methyl alcohol to the powder mixture.
And after mixing, place the mill lid in an argon atmosphere.
And fired to evaporate the methyl alcohol,
Dry and then separately in an argon atmosphere
At the bottom of the prepared cylindrical container made of Ti,
Insert a WC-based cemented carbide disk and place it on top of this disk.
The mixed powder is charged, pressed with a push rod and filled.
Place a WC-based cemented carbide disk on the mixed powder, and then
After taking it out of the atmosphere of Lugon, put on the top lid made of Ti
Press and press to mix the powder mixture in the Ti cylindrical container.
Compress the thickness and subsequently dissolve the top lid in the cylindrical container
Touch and seal it, thus filling the above mixed powder
And sealed the cylindrical container into the ultra-high pressure and ultra-high temperature generator
And maximum applied pressure: 4-5 GPa, temperature range: 1300-
After holding at 1500 ° C, release pressure after cooling
Is performed, an Al 2 O 3 layer is interposed between the carbon nitride of the metal forming the binder phase in the CBN-based sintered material and the CBN particles, that is, the surface of the CBN particles is continuously or intermittently surrounded by Al 2 O 3. When the layer is formed, the Al 2 O 3 surrounding layer has excellent adhesion to both the CBN particles and the binder phase. Therefore, even if high-speed cutting is performed using this as a cutting tool, Since the falling off of the steel is remarkably suppressed, the research results have shown that the steel exhibits more excellent wear resistance and shows excellent cutting performance over a long period of time.

【0005】この発明は、上記研究結果にもとづいてな
されたもので、原料粉末として、1〜10μmの範囲内
の所定の平均粒径を有するCBN粉末、金属の炭窒化物
粉末およびAl 2 3 粉末、さらにAl(OH) 3 粉末を用
意し、まず前記CBN粉末と前記Al(OH) 3 粉末とを
NH 4 OH溶液の中で撹拌混合した後、乾燥することに
よりAl 2 3 で包まれたAl 2 3 包囲CBN粉末を調整
し、これら原料粉末を配合し、これらの配合粉末を、そ
れぞれWC基超硬合金で内張りされた粉砕ミル内に装入
し、さらに前記配合粉末に対してメチルアルコールを加
えて混合し、混合後、前記ミルの蓋をアルゴン雰囲気中
で開放し、加焼して前記メチルアルコールを蒸発させ、
乾燥し、ついで同じくアルゴン雰囲気内において、別途
用意したTi製円筒型容器の底部に、まず同じく別途用
意したWC基超硬合金製円板を装入し、この円板上に上
記混合粉末を装入し、押し棒で押えて充填し、この充填
混合粉末上にWC基超硬合金製円板を敷置し、つぎにア
ルゴン雰囲気から取りだした後、さらにTi製上蓋をか
ぶせてプレスして前記Ti製円筒型容器内の混合粉末の
厚みを圧縮し、引続いて前記円筒型容器に前記上蓋を溶
接して、これを密封し、このように上記混合粉末を充填
して密封した円筒型容器を超高圧超高温発生装置に装入
し、最高付加圧力:4〜5GPa、温度範囲:1300〜
1500℃の条件で保持した後、冷却についで圧力解放
を行うことを特徴とする、結合相形成成分としてのT
i、ZrおよびHfの炭化物、窒化物および炭窒化物のう
ち1種または2種以上:20〜40vol%、酸化アルミニ
ウム:6〜40vol%、分散相形成成分としての立方晶窒
化ほう素:残り、からなる配合組成、並びに上記酸化ア
ルミニウムのうち全体に占める割合で1〜20vol%は、
立方晶窒化ほう素粒子の表面部に連続または断続包囲層
を形成し、残りの酸化アルミニウムは結合相中に分散し
て存在する組織を有し、実質的に配合組成と同一の成分
組成を有する耐摩耗性に優れた立方晶窒化ほう素基超高
圧焼結材料の製造方法に特徴を有するものである。
The present invention has been made on the basis of the above research results, and has a raw material powder within a range of 1 to 10 μm.
Powder having a predetermined average particle size, metal carbonitride
For powder, Al 2 O 3 powder, and Al (OH) 3 powder
First, the CBN powder and the Al (OH) 3 powder
After stirring and mixing in an NH 4 OH solution,
Adjusting the Al 2 O 3 enclosing CBN powder wrapped in more Al 2 O 3
Then, these raw material powders are blended, and these blended powders are
Each is charged into a grinding mill lined with WC-base cemented carbide
And adding methyl alcohol to the powder mixture.
And after mixing, place the mill lid in an argon atmosphere.
And fired to evaporate the methyl alcohol,
Dry and then separately in an argon atmosphere
At the bottom of the prepared cylindrical container made of Ti,
Insert a WC-based cemented carbide disk and place it on top of this disk.
The mixed powder is charged, pressed with a push rod and filled.
Place a WC-based cemented carbide disk on the mixed powder, and then
After taking it out of the atmosphere of Lugon, put on the top lid made of Ti
Press and press to mix the powder mixture in the Ti cylindrical container.
Compress the thickness and subsequently dissolve the top lid in the cylindrical container
Touch and seal it, thus filling the above mixed powder
And sealed the cylindrical container into the ultra-high pressure and ultra-high temperature generator
And maximum applied pressure: 4-5 GPa, temperature range: 1300-
After holding at 1500 ° C, release pressure after cooling
And performing, T as binder phase forming component
i, one or more of carbides, nitrides and carbonitrides of Zr and Hf: 20 to 40 vol%, aluminum oxide: 6 to 40 vol%, cubic boron nitride as a dispersed phase forming component: remaining, 1-20 vol% in the total composition of the above-mentioned aluminum oxide,
A continuous or intermittent envelope layer is formed on the surface of the cubic boron nitride particles, and the remaining aluminum oxide has a structure dispersed and present in the binder phase, and has substantially the same composition as the composition.
The present invention is characterized by a method for producing a cubic boron nitride-based ultrahigh-pressure sintered material having a composition and excellent wear resistance.

【0006】次に、この発明のCBN基超高圧焼結材料
の製造方法において、組成を上記の通り限定した理由を
説明する。 (a) 金属の炭窒化物 これらの成分は、耐熱性と焼結性を向上させる作用があ
るが、その割合が20%未満では、前記作用に所望の向
上効果が得られず、一方その割合が40%を越えると、
耐摩耗性が低下するようになることから、その割合を2
0〜40%と定めた。(b) Al23 Al23には強度を向上させる作用があるが、その割合
が6%未満では、所望の強度向上効果が得られず、一方
その割合が40%を越えると耐摩耗性が低下する様にな
ることから、その割合を6〜40%と定めた。 (c)Al23包囲層 Al23包囲層は、分散相形成成分であるCBN粒子と
結合相形成成分である金属の炭窒化物のいずれに対して
も優れた密着性を持つことから、Al23でCBN粒子
の包囲層を形成することにより、CBN粒子と金属の炭
窒化物との結合強度が一段と向上し、この結果CBN粒
子の脱落が著しく抑制され、耐摩耗性の顕著な向上がも
たらされるようになるが、その割合が全体に占める割合
で1%未満では、前記作用に所望の効果が得られず、一
方その割合が20%を越えると包囲層の厚さが大きくな
り過ぎて、耐摩耗性が低下するようになることから、そ
の割合を全体に占める割合で1〜20%と定めた。
Next, the CBN-based ultra-high pressure sintered material of the present invention
The reason why the composition is limited as described above in the production method described above will be described. (a) Metal carbonitrides : These components have the effect of improving heat resistance and sinterability, but if their proportion is less than 20%, the desired effect cannot be obtained in the above-mentioned effects. When the ratio exceeds 40%,
Since the wear resistance is reduced, the ratio is set to 2
It was set to 0 to 40%. (b) Al 2 O 3 : Al 2 O 3 has an effect of improving strength, but if its proportion is less than 6%, the desired effect of improving strength cannot be obtained, while if its proportion exceeds 40%, Since the abrasion resistance is reduced, the ratio is set to 6 to 40%. (c) Al 2 O 3 surrounding layer : The Al 2 O 3 surrounding layer has excellent adhesion to both CBN particles as a disperse phase forming component and metal carbonitride as a binder phase forming component. Therefore, by forming the envelope layer of the CBN particles with Al 2 O 3 , the bonding strength between the CBN particles and the carbonitride of the metal is further improved, and as a result, the falling off of the CBN particles is significantly suppressed, and the wear resistance is improved. However, if the ratio is less than 1% of the total, the desired effect cannot be obtained in the above-mentioned operation, while if the ratio exceeds 20%, the thickness of the surrounding layer is not increased. Becomes too large and the abrasion resistance is reduced, so that the ratio is set to 1 to 20% in the whole.

【0007】[0007]

【実施例】 ついで、この発明のCBN基超高圧焼結材
の製造方法を実施例により具体的に説明する。原料粉
末として、1〜10μmの範囲内の所定の平均粒径を有
するCBN粉末、各種の金属の炭窒化物粉末およびAl
23粉末、さらにAl(OH)3粉末を用意し、まず前記
CBN粉末と前記Al(OH)3粉末とをNH4OH溶液の
中で撹拌混合した後、130℃で乾燥することにより表
1に示される割合のAl23で包まれたAl23包囲C
BN粉末を調整し、これら原料粉末をそれぞれ表1に示
される配合組成に配合し、これらの配合粉末を、それぞ
れWC基超硬合金で内張りされた粉砕ミル内に装入し、
さらに前記配合粉末に対して40容量%のメチルアルコ
ールを加えて24時間混合し、混合後、前記ミルの蓋を
アルゴン雰囲気中で開放し、温度:130℃に加焼して
前記メチルアルコールを蒸発させ、乾燥し、ついで同じ
くアルゴン雰囲気内において、別途用意した内径:10
mφ×高さ:15mmの寸法をもったTi製円筒型容器の底
部に、まず同じく別途用意した直径:9.8mmφ×厚
さ:2mmの寸法をもったWC基超硬合金製円板を装入
し、この円板上に厚みが7mmとなるように上記混合粉末
を装入し、押し棒で軽く押えて充填し、この充填混合粉
末上に厚さ2mmのWC基超硬合金製円板を敷置し、つぎ
にアルゴン雰囲気から取りだした後、さらにTi製上蓋
をかぶせてプレスして前記Ti製円筒型容器内の混合粉
末の厚みを5.5mmに圧縮し、引続いて前記円筒型容器
に前記上蓋を溶接して、これを密封し、このように上記
混合粉末を充填して密封した円筒型容器を公知の超高圧
超高温発生装置に装入し、最高付加圧力:4〜5GPa、
温度範囲:1300〜1500℃の条件で30分間保持
した後、冷却についで圧力解放を行うことによって、実
質的に配合組成と同一の成分組成を有し、かつ上記WC
基超硬合金製の上下円板に拡散結合した状態の本発明
よるCBN基超高圧焼結材料1〜9をそれぞれ製造し
た。なお、表2に示させる通り、CBN粉末へのAl2
3包囲層の形成を行う以外は同一の条件で、従来CB
N基超高圧焼結材料1〜9を製造した。
EXAMPLES Next, the method for producing a CBN-based ultrahigh-pressure sintered material of the present invention will be specifically described with reference to Examples. CBN powder having a predetermined average particle size in the range of 1 to 10 μm, carbonitride powder of various metals, and Al
2 O 3 powder and further Al (OH) 3 powder are prepared, and the CBN powder and the Al (OH) 3 powder are first stirred and mixed in an NH 4 OH solution, and then dried at 130 ° C. Al 2 O 3 surrounding C wrapped with Al 2 O 3 in the proportions shown in FIG.
BN powder was prepared, these raw material powders were respectively blended into the blending composition shown in Table 1, and these blended powders were respectively charged into a grinding mill lined with a WC-based cemented carbide,
Further, 40% by volume of methyl alcohol was added to the blended powder and mixed for 24 hours. After mixing, the lid of the mill was opened in an argon atmosphere, and the mill was evaporated to a temperature of 130 ° C. to evaporate the methyl alcohol. And then dried, and then prepared in the same manner in an argon atmosphere by using a separately prepared inner diameter: 10
At the bottom of a cylindrical container made of Ti having a size of mφ × height: 15 mm, a disk made of a WC-based cemented carbide having a size of 9.8 mmφ × thickness: 2 mm prepared separately was first mounted on the bottom of a cylindrical cylindrical container made of Ti. Then, the mixed powder is charged into the disc so as to have a thickness of 7 mm, lightly pressed with a push rod and filled, and a 2 mm-thick WC-based cemented carbide disc is placed on the filled mixed powder. And then taken out of the argon atmosphere, further covered with a Ti top cover and pressed to compress the mixed powder in the Ti cylindrical container to a thickness of 5.5 mm. The upper lid is welded to the container, which is sealed, and the cylindrical container thus filled and sealed with the mixed powder is charged into a known ultra-high pressure and ultra-high temperature generator, and the maximum applied pressure is 4 to 5 GPa. ,
Temperature range: After holding at 1300 to 1500 ° C. for 30 minutes, the pressure is released after cooling, so that the WC has substantially the same composition as the compounded composition and the WC
The present invention in a state where diffusion bonded to the base cemented carbide of the upper and lower disc
The CBN group ultrahigh pressure sintered material 1-9 by manufactured respectively. In addition, as shown in Table 2, Al 2
Under the same conditions except that the O 3 envelope layer is formed, the conventional CB
N-based ultra-high pressure sintered materials 1 to 9 were produced.

【0008】つぎに、上記本発明によるCBN基超高圧
焼結材料1〜9と従来CBN基超高圧焼結材料1〜9を
別途用意した四角形状のWC基超硬合金製チップに銀ろ
うによって固定し、さらにノーズRを0.4mmに仕上げ
て切削工具とし、被削材:浸炭焼入鋼(ロックウェル硬
さ:60)、切削速度:200m/min、送り:0.08m
m/rev、切込み:0.1mm、の条件での高硬度鋼の連続
高速切削試験を行い、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
を表1、2に示した。)
[0008] Next, the silver solder in a square shape of WC-based cemented carbide tip with CBN based ultrahigh pressure sintered material 1-9 a conventional CBN based ultrahigh pressure sintered material 1-9 were separately prepared according to the aforementioned present invention Fixed, and finished the nose radius to 0.4 mm to make a cutting tool. Work material: carburized hardened steel (Rockwell hardness: 60), cutting speed: 200 m / min, feed: 0.08 m
A continuous high-speed cutting test was performed on high-hardness steel under the conditions of m / rev and a depth of cut of 0.1 mm, and 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 Tables 1 and 2.)

【0009】[0009]

【表1】 [Table 1]

【0010】[0010]

【表2】 [Table 2]

【0011】[0011]

【発明の効果】 表1、2に示される結果から本発明
よるCBN基超高圧焼結材料1〜9は、従来CBN基超
高圧焼結材料1〜9に比べ、これを切削工具として用
い、高硬度鋼の高速切削を行った場合、いずれも一段と
優れた対摩耗性を示し、長期に亘って優れた切削性能を
発揮することが明らかである。
According to the present invention , based on the results shown in Tables 1 and 2 ,
The CBN-based ultra-high pressure sintered materials 1 to 9 according to the present invention are much better than the conventional CBN-based ultra-high pressure sintered materials 1 to 9 when they are used as cutting tools and high-speed cutting of high hardness steel is performed. It is clear that it shows wear resistance and exhibits excellent cutting performance over a long period of time.

───────────────────────────────────────────────────── フロントページの続き (58)調査した分野(Int.Cl.7,DB名) C04B 35/583 - 35/5835 ──────────────────────────────────────────────────続 き Continued on front page (58) Field surveyed (Int.Cl. 7 , DB name) C04B 35/583-35/5835

Claims (1)

(57)【特許請求の範囲】(57) [Claims] 【請求項1】 原料粉末として、1〜10μmの範囲内
の所定の平均粒径を有するCBN粉末、金属の炭窒化物
粉末およびAl 2 3 粉末、さらにAl(OH) 3 粉末を用
意し、まず前記CBN粉末と前記Al(OH) 3 粉末とを
NH 4 OH溶液の中で撹拌混合した後、乾燥することに
よりAl 2 3 で包まれたAl 2 3 包囲CBN粉末を調整
し、これら原料粉末を配合し、これらの配合粉末を、そ
れぞれWC基超硬合金で内張りされた粉砕ミル内に装入
し、さらに前記配合粉末に対してメチルアルコールを加
えて混合し、混合後、前記ミルの蓋をアルゴン雰囲気中
で開放し、加焼して前記メチルアルコールを蒸発させ、
乾燥し、ついで同じくアルゴン雰囲気内において、別途
用意したTi製円筒型容器の底部に、まず同じく別途用
意したWC基超硬合金製円板を装入し、この円板上に上
記混合粉末を装入し、押し棒で押えて充填し、この充填
混合粉末上にWC基超硬合金製円板を敷置し、つぎにア
ルゴン雰囲気から取りだした後、さらにTi製上蓋をか
ぶせてプレスして前記Ti製円筒型容器内の混合粉末の
厚みを圧縮し、引続いて前記円筒型容器に前記上蓋を溶
接して、これを密封し、このように上記混合粉末を充填
して密封した円筒型容器を超高圧超高温発生装置に装入
し、最高付加圧力:4〜5GPa、温度範囲:1300〜
1500℃の条件で保持した後、冷却についで圧力解放
を行うことを特徴とする、結合相形成成分としてのT
i、ZrおよびHfの炭化物、窒化物および炭窒化物のう
ち1種または2種以上:20〜40vol%、酸化アルミニ
ウム:6〜40vol%、分散相形成成分としての立方晶窒
化ほう素:残り、からなる配合組成、並びに上記酸化ア
ルミニウムのうち全体に占める割合で1〜20vol%は、
立方晶窒化ほう素粒子の表面部に連続または断続包囲層
を形成し、残りの酸化アルミニウムは結合相中に分散し
て存在する組織を有し、実質的に配合組成と同一の成分
組成を有する耐摩耗性に優れた立方晶窒化ほう素基超高
圧焼結材料の製造方法
Claims: 1. A raw material powder within a range of 1 to 10 μm.
Powder having a predetermined average particle size, metal carbonitride
For powder, Al 2 O 3 powder, and Al (OH) 3 powder
First, the CBN powder and the Al (OH) 3 powder
After stirring and mixing in an NH 4 OH solution,
Adjusting the Al 2 O 3 enclosing CBN powder wrapped in more Al 2 O 3
Then, these raw material powders are blended, and these blended powders are
Each is charged into a grinding mill lined with WC-base cemented carbide
And adding methyl alcohol to the powder mixture.
And after mixing, place the mill lid in an argon atmosphere.
And fired to evaporate the methyl alcohol,
Dry and then separately in an argon atmosphere
At the bottom of the prepared cylindrical container made of Ti,
Insert a WC-based cemented carbide disk and place it on top of this disk.
The mixed powder is charged, pressed with a push rod and filled.
Place a WC-based cemented carbide disk on the mixed powder, and then
After taking it out of the atmosphere of Lugon, put on the top lid made of Ti
Press and press to mix the powder mixture in the Ti cylindrical container.
Compress the thickness and subsequently dissolve the top lid in the cylindrical container
Touch and seal it, thus filling the above mixed powder
And sealed the cylindrical container into the ultra-high pressure and ultra-high temperature generator
And maximum applied pressure: 4-5 GPa, temperature range: 1300-
After holding at 1500 ° C, release pressure after cooling
And performing, T as binder phase forming component
i, one or more of carbides, nitrides and carbonitrides of Zr and Hf: 20 to 40 vol%, aluminum oxide: 6 to 40 vol%, cubic boron nitride as a dispersed phase forming component: remaining, 1-20 vol% in the total composition of the above-mentioned aluminum oxide,
A continuous or intermittent envelope layer is formed on the surface of the cubic boron nitride particles, and the remaining aluminum oxide has a structure dispersed and present in the binder phase, and has substantially the same composition as the composition.
A method for producing a cubic boron nitride based ultra-high pressure sintered material having a composition and excellent wear resistance.
JP27534793A 1993-11-04 1993-11-04 Method for producing cubic boron nitride based ultra-high pressure sintered material with excellent wear resistance Expired - Fee Related JP3146803B2 (en)

Priority Applications (1)

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JP27534793A JP3146803B2 (en) 1993-11-04 1993-11-04 Method for producing cubic boron nitride based ultra-high pressure sintered material with excellent wear resistance

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP27534793A JP3146803B2 (en) 1993-11-04 1993-11-04 Method for producing cubic boron nitride based ultra-high pressure sintered material with excellent wear resistance

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JPH07133154A JPH07133154A (en) 1995-05-23
JP3146803B2 true JP3146803B2 (en) 2001-03-19

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* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US7932199B2 (en) 2004-02-20 2011-04-26 Diamond Innovations, Inc. Sintered compact
US8500834B2 (en) 2004-02-20 2013-08-06 Diamond Innovations, Inc. Sintered compact
WO2010032137A1 (en) 2008-09-17 2010-03-25 Diamond Innovations, Inc. Cubic boron nitride ceramic composites and methods of making thereof
JP6098882B2 (en) * 2013-05-30 2017-03-22 三菱マテリアル株式会社 Cubic boron nitride sintered body cutting tool with excellent fracture resistance

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