JPS5997579A - Composite sintered body and manufacture - Google Patents
Composite sintered body and manufactureInfo
- Publication number
- JPS5997579A JPS5997579A JP20713982A JP20713982A JPS5997579A JP S5997579 A JPS5997579 A JP S5997579A JP 20713982 A JP20713982 A JP 20713982A JP 20713982 A JP20713982 A JP 20713982A JP S5997579 A JPS5997579 A JP S5997579A
- Authority
- JP
- Japan
- Prior art keywords
- sintered body
- solid solution
- cermet
- wbn
- carbide
- 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.)
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- Ceramic Products (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】
本発明は、高硬度、耐摩耗性、靭性、耐熱性及び耐食性
に優れ、一般の鋼及び鋳鉄から難削材である焼入れ合金
鋼、浸炭材、ステンレス鋼及び高ニッケル合金等の切削
工具並びに軸受、ワークレスト及び巌す1きダイス等の
耐摩粍工具に適した複合焼結体及びその製造方法に関す
る。DETAILED DESCRIPTION OF THE INVENTION The present invention applies to hardened alloy steels, carburized materials, stainless steels, and high nickel steels, which are difficult-to-cut materials that have high hardness, wear resistance, toughness, heat resistance, and corrosion resistance. The present invention relates to a composite sintered body suitable for cutting tools such as alloys, and wear-resistant tools such as bearings, work rests, and dies, and a method for manufacturing the same.
従来のCB1〜および/またrt、W B iN f含
有する嶋密度相窒化硼素焼結体と超硬合金又はサーメッ
トとが回漕結付した榎曾滋結体は、高冨度相窒化硼素焼
結体部分茫CBNおよび/またはWBNと結合相とから
成る焼結体として判断したとき、績@相によって大別す
ると第1に結合相が金属又は合金から成っているもの、
第2に結合相が単−化合物又rt、複合化合物から成っ
ているもの、第3に結合相が金属又は合金と単−化合物
又は複合化合物とから成っているものとの3樵鵠カ4る
。この内温1の結合相から成る焼結体は、結合相の硬度
が低く高温でe、i史に軟化し易いために離□り材等の
熱発生全件う破nt+材を切削するときには極端に耐摩
耗性が劣ると云う欠点がMり、第2の結合相から成る焼
結体は、結合相の硬度が高く高温での硬度低下も少ない
のに対し靭性が低く断続的切削条件で使用するとチッピ
ング又は欠損等を起し易いと云う欠点が有り、第3の結
合相から成る焼結体は、結合相中の金沃又は合金の量が
多くなると硬度が低く嶋渦では更に軟化し易く、結合相
中の単−化合物又は複合化合物の量が多くなると硬度が
篩く靭性が低下し、単に第1(/:)結合相と第2の結
合相の中間四特性に有ると云う+f−iJ題点がある。A conventional Enoji body in which a high-density phase boron nitride sintered body containing CB1~ and/or rt, W BiN f and a cemented carbide or cermet is circularly bonded is a high-density phase boron nitride sintered body. When judged as a sintered body consisting of CBN and/or WBN in the body part and a binder phase, it can be broadly classified by phase: first, those in which the binder phase is made of metal or alloy;
Second, the binder phase is composed of a single compound, rt, or composite compound; and third, the binder phase is composed of a metal or alloy and a single compound or a composite compound. . This sintered body consisting of a binder phase with an internal temperature of 1 has a low hardness and is easily softened at high temperatures. The disadvantage is that the wear resistance is extremely poor, and the sintered body made of the second binder phase has a high hardness of the binder phase and little decrease in hardness at high temperatures, but has low toughness and cannot be used under intermittent cutting conditions. It has the disadvantage that chipping or chipping is likely to occur when used, and the sintered body made of the third binder phase has a low hardness and becomes even softer in the Shima vortex when the amount of gold or alloy in the binder phase increases. It is easy to say that when the amount of a single compound or a composite compound in the binder phase increases, the hardness increases and the toughness decreases, and the properties are simply in the middle between the first (/:) binder phase and the second binder phase. -iJ There is a problem.
又、高密度相A化#め素焼結体と超硬台金又はサーメッ
トを回漕結付する場合、常圧で載祠を介在させて接合す
る方法とMi關圧薗温Fで回漕結付する方法がある。こ
の内脈材を介在させて接合し7″cものは、扁密度相屋
化硼素焼結体と超映合金又Cより−メットとの両方に(
需れ性の艮い鑞材がないために接・ケ頻度が低かったり
、鑞材が高温で軟化するために塑性変形が生じると太う
問題が有り、超商圧高温下で固着結合したものは、旨田
腿相窒化硼素焼結本と超硬台金又はサーメットとの反応
性等が悪く固着結合部に空孔が生じ同層強度が低下する
と云う問題がめる。In addition, when rotary bonding a high-density phase A #metallic sintered body and a cemented carbide base metal or cermet, there are two methods: bonding with an intervening abrasion at normal pressure, and rotary bonding at a Mi-related pressing temperature F. There is a way. A 7"c piece joined with this inner vein material is made of both the densified boron sintered body and the super-alloy or C-met (
There is a problem that the frequency of joining is low because there is no solder material that is in demand, or that the solder material softens at high temperatures and becomes thicker when plastic deformation occurs. This poses a problem in that the reactivity between the Umada phase boron nitride sintered base and the cemented carbide base metal or cermet is poor, resulting in the formation of pores in the bonded joint, resulting in a decrease in the strength of the same layer.
本発明は、上述のような従来の欠点及び問題点全除去し
、高硬度、耐熱性、耐食性及び高温強度に優れしかも耐
摩耗性及び靭性全高めた高密度相窒化(dl累焼績体と
超硬合金又はサーメットとの固着結合強度をも同時に高
めに仮台焼結体及びその製造方法である。fi’lJち
本発明の複合焼結体は、40〜80捧績チのCBNおよ
び/またはWBNと20〜60捧績チの結合相と不し:
If避不純物から成る焼結挿と)イ(硬a蛍又はサーメ
ットとが強固に固層+Iii¥汗し/こ叡ば体であって
、このCBNBよび/またはWi3へ伊含有した焼結体
の結合相がJj!8結体の141比C2〜40%の(’
l’ i、W、Ta)CN又は(’l’i、W、 ’I
” a、 N b ) CNのBl型固溶体と6〜40
%の′■゛1、’lr、 kif%Ta、 Nb、 V
の1棟以上の窒化物、炭窒化物もしくはこれらの相互固
溶体化@物と1〜20%のA4.、S i、 T i。The present invention completely eliminates the above-mentioned conventional drawbacks and problems, and provides a high-density phase nitrided (DL) composite material that has excellent hardness, heat resistance, corrosion resistance, and high-temperature strength, as well as improved wear resistance and toughness. The composite sintered body of the present invention is a temporary sintered body that has a high bonding strength with cemented carbide or cermet, and a method for manufacturing the same. Or with or without WBN and a bonding phase of 20-60 hours:
If the sintered insert consisting of avoided impurities and the sintered body of the CBNB and/or Wi3 are strongly solidified with hard alumina or cermet, The bonded phase is 141 ratio C2~40% of Jj!8 aggregate ('
l'i, W, Ta) CN or ('l'i, W, 'I
"a, Nb) Bl type solid solution of CN and 6 to 40
%'■゛1,'lr, kif%Ta, Nb, V
One or more nitrides, carbonitrides, or mutual solid solution of these and 1 to 20% of A4. , S i, T i.
Zr、 1−1f、 k”e、 N i、 Coの2独
以上から成る金属間化合物および/またはAt、Si、
Ti、Zr。Intermetallic compound consisting of two or more of Zr, 1-1f, k”e, Ni, Co and/or At, Si,
Ti, Zr.
Hf、 i”e、 Ni、 Coの13以上の硼化物、
硼窒化物もしくはこれらの相互固溶体化合物と0.1〜
20%の粒界析出したWC4−含有した焼結体で、この
焼結体が超硬合金又はサーメットと強固に固M結合して
なる複合焼結体である。このような複合9′h結体の尚
蜜度相家化イ1lIII累焼結体は、焼結過程において
粒界析出したWCがCBNおよび/ま友はWBNと結合
相中の他の化合物との各粒子表面に微、Nll W C
粒子として析出しているためにc 13 Nおよび/ま
たはWBNと結合相との結合強度を品め、結合相内の各
粒子間の結合う天産も高めたものと考えら九る。このよ
うに粒界析出した倣剛WC粒子が晶密匿相窒化硼素g!
8結体内の各粒子間の結合媒介的作用となっていること
から高¥fi度相窒化硼素焼結体の靭性及び強度が著し
く向上し、粒界析出したWCが倣細であるために硬さも
高く、結合相中のBl型固溶体と細化合物の高い硬裏と
共に耐At耗性に寄与し、WC粒子の析出反応に伴って
生じたAt、 S i、 ’1” i、Zr、 Mf、
Fe、 Ni。13 or more borides of Hf, i”e, Ni, Co,
0.1 to boronitride or their mutual solid solution compound
This is a composite sintered body containing 20% of WC4 precipitated at grain boundaries, and this sintered body is firmly M bonded to a cemented carbide or cermet. In such composite 9'h compacts, WC precipitated at grain boundaries during the sintering process is mixed with CBN and/or WBN and other compounds in the binder phase. On the surface of each particle, there is a fine amount of Nll W C
It is thought that because it is precipitated as particles, it improves the bonding strength between c 13 N and/or WBN and the binder phase, and also increases the bond strength between each particle in the binder phase. The imitatively rigid WC grains precipitated at the grain boundaries in this way form the crystal-dense phase boron nitride g!
The toughness and strength of the high-finess phase boron nitride sintered body are significantly improved due to the bond-mediated effect between each particle in the 8-crystal, and the WC precipitated at the grain boundary is fine and hard. The Bl-type solid solution in the binder phase and the high hardness of fine compounds contribute to the At wear resistance, and the At, Si, '1'' i, Zr, Mf,
Fe, Ni.
Coの2棟以上から成る金属間化合物および、/または
Az、 S i、 Ti、 Zr、 1−1f、 Fe
、 Ni、 C。Intermetallic compound consisting of two or more buildings of Co and/or Az, Si, Ti, Zr, 1-1f, Fe
, Ni, C.
の1種以上の+jl化物、硼窒化物もしくはこれらの相
互固溶体化合物が焼結体の緻密化を促進すると共に高温
における耐摩耗性を尚め、特に1゛11Zr、klf
の+/III化物が高温における耐摩耗性の同上に宥与
しくいる高密度相窒化軸素焼結体である。One or more +jl oxides, boronitrides, or mutual solid solution compounds thereof promote the densification of the sintered body and improve wear resistance at high temperatures.
This is a high-density phase nitrided axonal sintered body in which the +/III compound of +/III provides excellent wear resistance at high temperatures.
しかもこのような高密度相窒化硼素焼結体中に析出した
WC粒子は、超硬合金又はサーメットに含イ了している
鉄族金属との濡れ性が良好なこと及び超硬台金又はサー
メット中の戻化物金主体としfc他化合物との表面拡散
の容易性とによって尚@夏相屋化171素焼軸体と超硬
合金又はサーメットと金緻密で強国に固着結合した複合
焼結体である。Moreover, the WC particles precipitated in such a high-density phase boron nitride sintered body have good wettability with iron group metals contained in the cemented carbide or cermet, and Due to the fact that the recured compound is mainly gold inside and the surface diffusion of fc and other compounds is easy, it is a composite sintered body in which the unglazed shaft, cemented carbide or cermet, and gold are densely bonded and firmly bonded. .
本発明の複合焼結体の製造方法は、出発原料として40
〜80体槓チのCBNおよび/またはWBNと2〜40
体積−の第1図に表わすA、B、C,Dの線上及び各点
内にあるBll型化化物固溶体但し、T a Cに対し
て30%以下1dNbcで置換しても焼結体の特性が変
らないので良いンAは、40モル%TiC−50モル%
WC−10モル%TaC
Bは、55モル%TiC−35モIL/%we−toモ
ル%’1’ a C
Cは、40モルチ゛l’1c−20モル%WC−40モ
ル襲’ra C
Jハよ、25モル%TiC−35モ)し%WC−40モ
ル・%TaC
と6〜°40体O1j%の’1’ i、 Z r、 H
f、 T a、 tN b。The method for producing a composite sintered body of the present invention uses 40% as a starting material.
~80 units of CBN and/or WBN and 2-40
Bll type compound solid solution on the lines A, B, C, D and within each point shown in Figure 1 of the volume. A is good because it does not change 40 mol% TiC-50 mol%
WC-10 mol% TaC B is 55 mol% TiC-35 mol% IL/%we-to mol%'1' a C is 40 mol% 1c-20 mol% WC-40 mol% 'ra C J Ha, 25 mol % TiC-35 mo) and % WC-40 mol % TaC and 6 to 40 bodies O1j% '1' i, Z r, H
f, T a, tN b.
Vの1独以上の窒化物もしくはこれらの相互1ml溶体
窒化:勿と1〜20体$矛のAt、 8 i、 ’f
i、Zr、Hf の1橿以上の金鞠又は合金と金混合粉
砕後成形した粉末圧粉体を超硬合金又はサーメットから
成る’AAW塊体の腕体くとも一面に#0:触させて圧
力40〜60Kb、温度1200〜1500℃の萬密度
相窒化硼素の安定な領域で焼結することによって超硬合
金又はサーメットから成る焼結腕木に含有しているFe
、Ni、Coの1棟以上の金属又は合金を高密度相窒化
硼素焼結体中に滲透拡散させることもできる。又、筒密
度相窒化硼素焼結体内に滲透拡散させるに’e、 1’
Ji、 Co01棟以上の金属又は合金の量?多くする
ために出発原料として40〜80体績矛のCBNおよび
/またはWBNと2〜40体績襲の第1図に表わすA、
B。One or more nitrides of V or their mutual 1ml solution nitridation: Of course, 1 to 20 units of At, 8i, 'f
A powder compact formed by mixing and crushing one or more metal balls or alloys of i, Zr, and Hf with gold is brought into contact with one side of the arm body of an 'AAW lump made of cemented carbide or cermet. Fe contained in a sintered arm made of cemented carbide or cermet is produced by sintering in a stable region of tensic phase boron nitride at a pressure of 40 to 60 Kb and a temperature of 1200 to 1500°C.
, Ni, and Co can also be diffused into the dense phase boron nitride sintered body. In addition, 'e, 1' is used to permeate and diffuse into the cylindrical density phase boron nitride sintered body.
Ji, amount of metal or alloy of Co01 or more? In order to increase the starting material, 40 to 80 samples of CBN and/or WBN and 2 to 40 samples of A as shown in Figure 1,
B.
C,D線上及び′谷点内にめるBl型戻イヒ9勿j司Y
d体(但し、racにズうして30%以下ri Nb
Cで置換しでも艮い)と6〜40体績チのri、Zr、
)if、 ’l’a、 Nb、 Vの1徨以上の窒化物
もしくはこれらの相互回溶捧侑化物と?混合粉伜俊成形
しく五、ま
た粉末d体とこの粉末圧粉体の一田」にAj、Sl・・
1・1、Hl、V、i’e、 Ni、 Coの1棟以上
の全組又は付合から成る板状物体′k[触させ、この板
状物体の他面又ケ」粉末用粉本の他面に超硬台金又はサ
ーメットか(I蔵な腕体を接触設置して圧力40〜60
K b 、 77、、i1則1200〜1500℃の
超^圧編温下で焼結することによって板状物体から尚@
度相望化1jffll lA= m fE+’i (ト
内にA ts Sx % Hf % V%士l e 、
N 15Coの1 、I’ljf以−]二の金属又は
合金を滲透拡散させることも′r:きる。このように本
発明の複合焼結体の製造方法における高黄駄相窒化硼系
7に粘体の出発原料は、At、 S i、 T i、j
(f、 V、 Fe、Ni、 C。Place the Bl type back on the C and D lines and within the trough point.
d-form (however, less than 30% ri Nb compared to rac)
Even if it is replaced with C), 6-40 performance chi ri, Zr,
) if, 'l'a, Nb, nitride with one or more of V, or a mutually fused nitride of these? Aj, Sl...
1.1, A plate-shaped object consisting of a complete set or combination of one or more of Hl, V, i'e, Ni, Co [touch the other side of this plate-shaped object] Place a carbide base metal or cermet (I-shaped arm) in contact with the other side and apply a pressure of 40 to 60
K b , 77, , i1 rule 1200~1500℃ ultra-pressure knitting temperature to sinter the plate-like object to still @
Degree phase visualization 1jffll lA= m fE+'i (A ts Sx% Hf% V%shile in G,
It is also possible to permeate and diffuse the metals or alloys of N 15Co and I'ljf. As described above, the starting materials for the viscous material in the high-sodium-phase boron nitride system 7 in the method for producing a composite sintered body of the present invention are At, S i, T i, j
(f, V, Fe, Ni, C.
の1糧以上の金属又は合金全粉末状で添加する場合又は
板状物体によって滲透拡散させる場合史には粉末状の麻
加と板状物体からの滲透拡散とを組合せる場合でも良い
が金属又は台金の粉末は、微粉末になる佳は索及び水分
が膜層し易く、この吸着したポ素及び水分が密閉された
晶温尚圧ドでカス状になると焼結体の緻密化が直置され
るためtこ金!)う又は合金は板状物体からの滲透拡散
が服ましい。こ\で使用する板状物体は、各全編又は合
金の薄板でも良く、更にメッキ、−蒸着等の方法葡利用
することもできる。他の出発原料の内Bl型炭化吻固溶
体は、(’I’ i、 ’vV) CとT a Cとの
形態で冷加することも考えられるが焼結過程中昇温さn
るに従って各化合物元素の再配列とWCの析出が進行す
る段階でガス発生量が多くなシ、各粒子間の接触が減少
して相互拡散が匙りにく\なってWCの析出が困難にな
ることからBll型化化1+!l固溶(D 出%a3j
na、(4’ i、 W、 T a ) C又1ti(
T i、 W、 T a、 Nb ) Cの形態でぢ5
加する方法が望ましい。When one or more metals or alloys are added in whole powder form or permeated and diffused through a plate-like object, it is possible to combine powdered hemp and permeate-diffused from a plate-like object. The powder of the base metal becomes a fine powder, but it is easy to form a layer of carbon and moisture, and if this adsorbed porium and moisture become like a scum in a sealed crystal temperature and pressure chamber, the sintered body will become denser. I paid so much money to be done! ) or alloys are susceptible to seepage and diffusion from plate-like objects. The plate-shaped object used here may be a whole sheet or a thin plate of an alloy, and furthermore, methods such as plating and vapor deposition can also be used. Among the other starting materials, the Bl-type carbonized solid solution may be cooled in the form of ('I'i,'vV)C and T a C, but the temperature is raised during the sintering process.
As the rearrangement of each compound element progresses and the precipitation of WC progresses, a large amount of gas is generated, and the contact between each particle decreases, making it difficult for interdiffusion to occur, making it difficult to precipitate WC. Bll type 1+! l solid solution (D output %a3j
na, (4' i, W, T a ) C or 1ti (
Ti, W, Ta, Nb) Form of C5
It is preferable to add
本発明の複合焼結体の製造方法のように高密度相窒化硼
素焼結体の出発原料がCBNおよび/またはWBNとW
Cf析出する原料である(Ti。In the method for producing a composite sintered body of the present invention, the starting materials of the high-density phase boron nitride sintered body are CBN and/or WBN and WBN.
It is a raw material for Cf precipitation (Ti.
シV、Ta)C又は(’、I’ i、 W、 Ta、
Nb ) CのBl型炭化物固固溶体このBl型炭化物
固播体に侵入拡散してW(’の析出に寄与するT i、
Z r、 Hf。V, Ta) C or (', I' i, W, Ta,
Nb) Bl-type carbide solid solution of C penetrates and diffuses into this Bl-type carbide solid dispersion and contributes to the precipitation of W('Ti,
Zr, Hf.
′Pa51N+)、V の1種以上の窒化物もしくはこ
れらの相互固在f体嵯化゛吻と焼結過程で焼結助剤的作
用及びVVC,B1出促辿的作用k t 6 A t、
8 i 、 ’I” i 。'Pa51N+), one or more nitrides of V or their mutually solid f-body silting and sintering aid action in the sintering process and VVC, B1 promotion trace action k t 6 A t,
8 i, 'I''i.
Zr、Iff、 Fe、 Ni、Co の1種以上と
が尚温高圧下におかれると最初にAl、 S j、 ’
f i、Zr。When one or more of Zr, If, Fe, Ni, and Co are placed under high temperature and pressure, Al, S j, '
f i, Zr.
1(f、 i’e、 Ni、 Co (7)IIFJ以
上が塑性流動シテ他の各粒子の粒界に滲透しBl型炭化
物固溶体と’1” i、 Zr、 14f、 Ta、
Nb、 Vの1種以上の窒化物もしくはこれらの相互固
溶捧呈化物との各粒子の表面拡散音促進させることによ
り431型炭化吻固浴体の中のWとT i、 Zr、
Hf、 Ta、 Nb、 Vの1棟以上との拡散移動と
共に侵入型元素でめる屋素及び炭素の拡散移動が漱しく
なり、Bl型炭化物固溶体内に主として窒素元素が侵入
拡散することによってBl型炭化物中のWCが微細な粒
子として粒界析出してくると考えられる。又、焼結助剤
的作用とWC粒界析出の促進的作用金するAt、 8
i、 Ti、 Zr、 Hf、 F’e、 Ni、 C
oは、他の各粒子との濡れ性が良好なことから各粒子の
粒界に均一に滲透して各粒子の粒子成長を抑制すると共
に焼結が進行するに従ってCBNおよび/′iたdWf
3Nとも反応して焼結後は硼化物および/または+4窒
化吻として任在し、一部未反応又は過剰に存在したもの
が金lj4間化合物として存在するようになると考えら
れる。更に、尚密度相窒化イ/l累焼結体内に粒界析出
したWC粒子とAt。1 (f, i'e, Ni, Co (7) IIFJ or more permeates into the grain boundaries of each particle and forms a BL-type carbide solid solution and '1' i, Zr, 14f, Ta,
By promoting the surface diffusion sound of each particle with one or more nitrides of Nb, V or their mutual solid solution deposition, W, Ti, Zr,
Along with the diffusion movement with one or more of Hf, Ta, Nb, and V, the diffusion movement of nitrogen and carbon, which are interstitial elements, becomes stagnant, and the nitrogen element mainly enters and diffuses into the Bl type carbide solid solution, causing Bl It is thought that WC in the type carbide precipitates at grain boundaries as fine particles. In addition, At, which acts as a sintering aid and promotes WC grain boundary precipitation, 8
i, Ti, Zr, Hf, F'e, Ni, C
Since o has good wettability with other particles, it penetrates uniformly into the grain boundaries of each particle and suppresses the grain growth of each particle, and as sintering progresses, CBN and /'i dWf
It is thought that it also reacts with 3N and remains as a boride and/or +4 nitride after sintering, and that some unreacted or excessively present gold lj4 intercompounds exist. Furthermore, WC grains and At which precipitated at the grain boundaries within the dense phase nitrided I/l accumulated sintered body.
Sl、lpj、Zr、 Hf、 Fe、 Ni、 Co
(7)1棟以上特にFe、Ni、Co全含有してい
ると超硬合金又はサーメットとの複合焼結体となったと
きその接合面の固着結合強度が著しく痛くなる。Sl, lpj, Zr, Hf, Fe, Ni, Co
(7) If more than one structure contains all of Fe, Ni, and Co, the adhesion bond strength of the joint surface will be significantly impaired when a composite sintered body is formed with cemented carbide or cermet.
こ\で本発明の複合焼蛸体で数値限定した理由について
述べる。Here, we will discuss the reasons for limiting the numerical values for the composite baked octopus body of the present invention.
(a)CBNおよび/またはWBNの量CBNおよび/
またはWBNが40体積−未満では、高硬度なCBNお
よび/またはWBNの効果が弱くて耐摩耗性が低くなり
過ぎ、80体$係を越えて多くなると強度が低くなり過
ぎて離削材等の断続的切削条件で使用し難くなるために
茜密度相窒化備素y8結体内のCBNおよび/またはW
BN量は40〜80体槓楚とした。(a) Amount of CBN and/or WBN CBN and/or
If the WBN is less than 40 volume, the effect of high hardness CBN and/or WBN is weak and the wear resistance becomes too low, and if it exceeds 80 volume, the strength becomes too low and the wear resistance becomes too low. CBN and/or W in the madder density phase nitrided Y8 structure is difficult to use under intermittent cutting conditions.
The amount of BN was 40 to 80 bodies.
(b)Bl型固溶体の量
Bl型固浴体量が2体積−未満ではWCの粒界拍出が残
んど生じなく、40体積%を越えて多くなると相対的に
他の成分量が少なくなるが特にCBNおよび/またはW
BNiと′■゛1、Zr、Hf。(b) Amount of Bl-type solid solution If the amount of Bl-type solid solution is less than 2 volumes, grain boundary ejection of WC will not occur, but if it exceeds 40% by volume, the amount of other components will be relatively small. especially CBN and/or W
BNi and ′■゛1, Zr, Hf.
Ta、Nb、V の1棟以上の窒化物もしくは相互固
溶体窒化物の敏が少なくなることから耐摩れ性の低重が
生じる。このために16 密度相屋化#町素焼結体内の
Bl型固溶体量は、2〜40体桓チとした。The abrasion resistance is reduced because the nitrides or mutual solid solution nitrides of one or more of Ta, Nb, and V are less sensitive. For this purpose, the amount of Bl-type solid solution in the 16-density sintered body was set to 2 to 40 bodies.
又出発原料におけるBl型炭化物固浴体量を第1図のA
、B、C,Dの縁上及び各点を取り囲んだ所に限定した
理由は、A、D線を外れたWCの多い側ではWCの析出
量が多くなシ過ぎるのと出発原料として使用するときに
完全な固溶体が出来難いためであり、A、B線を外れた
TaCの少ない側では焼結体の耐熱性及び篩温での強度
低下となり5.B、C締金外れたTICの多い側ではW
Cが排出し藏くなり、C,i)巌を外れたTaCの多い
側では価格が高くなると共に焼結体の硬さが低F1唄回
になるために出発原料のBl型炭化吻固浴体Vユ、第1
図のA、B、c4 L)の線上及び谷点内とした。In addition, the amount of Bl type carbide solid bath in the starting material is indicated by A in Figure 1.
, B, C, and D and the areas surrounding each point are because the amount of WC precipitated is too large on the side with a lot of WC away from the A and D lines, and because it is used as a starting material. This is because sometimes it is difficult to form a complete solid solution, and on the side with less TaC outside the A and B lines, the heat resistance of the sintered body and the strength at the sieve temperature decrease.5. B, C On the side where there are many TICs that have come loose, W.
C is discharged and becomes black, and C, i) On the side where there is a large amount of TaC outside the peak, the price is high and the hardness of the sintered body becomes low F1, so the Bl type carbonization solid bath of the starting material is Body V Yu, 1st
It was placed on the lines A, B, c4 L) and within the trough points in the figure.
(c) T i、 Zr、 Hf、 Ta、 Nb、
Vの1独以上の窒化物、炭屋化物もしくはこれらの相
互同浴体化合力の重
上記量が6体積チ未満ではBl型固浴俸の中からWCケ
析出させる作用が弱く、40体積%全越えて多くなると
相対的に他の成分社が少なくなるが特にBl型固溶体と
焼結過程で焼結助剤的作用とW C41出の促進的作用
に薔与していると考えられるAt、 S i、 ’I’
j、 Zr、、Hf、 Fe%Ni、C。(c) Ti, Zr, Hf, Ta, Nb,
If the weight of one or more nitrides, charcoal compounds, or their mutual co-bath combination of V is less than 6 vol. If the amount exceeds that amount, other components will be relatively reduced, but At and S are thought to play a role as a sintering aid and a promoting effect on the production of WC41, especially in the Bl-type solid solution and sintering process. i, 'I'
j, Zr, , Hf, Fe%Ni, C.
01棟以上のjitが少なくなるために焼結体の緻密化
とWCの析出に支Kffi生じることから上記量は、6
〜40本積襲とした。Since the number of jits in buildings 01 and above decreases, the densification of the sintered body and the precipitation of WC are supported by Kffi, so the above amount is 6.
~40 pieces were accumulated.
(d) At、S i、 ’ri、 Zr、 Hf、
li’e、 Ni、 C。(d) At, S i, 'ri, Zr, Hf,
li'e, Ni, C.
の2独以上から成る金属間化@吻および/またはAty
Six Ti、 Z5 Hf、 Fe、 Ni、 C
oの1橿以上の棚化物又は硼窒化物の量
上記IWが1体積チ未イ両でtよ、焼結体の緻密化に支
降金生じ、20体槓%(f−超えて多くなると金椙同化
合向が多くなり過ぎて硬さが低下し耐M札・曲が劣る/
こめに上自己量は、1〜20体績矛とした。Intermetallicization consisting of two or more atoms @proboscis and/or Aty
Six Ti, Z5 Hf, Fe, Ni, C
The amount of shelving or boronitride of more than 1 volume of IW is less than 1 volume. The hardness decreases due to too much Kanasugi doubling, resulting in poor M tag resistance and bending.
In addition, the amount of self-sufficiency was set at 1 to 20.
(c) WCのべL界伯出量
wCの粒界排出量が0.1体積チ禾満では、0.1μi
n以ドの非常に機態なWCでありてもWC粒子の数が少
な過ぎて靭性及び強度低下−となり、20体積%r越え
て多くなるとWC粒子全析出させるのが困難をでなるた
めにWC粒界析出量は、0.1〜20体積チとした。(c) When the grain boundary discharge amount of WC is 0.1 volume, 0.1μi
Even if the WC is extremely mechanical, the number of WC particles is too small, resulting in a decrease in toughness and strength, and if the number exceeds 20% by volume, it becomes difficult to precipitate all the WC particles. The amount of WC grain boundary precipitation was 0.1 to 20 vol.
本発明は、ガードル型、ベルト型等の超高圧装置を使用
して焼結することができる。In the present invention, sintering can be performed using an ultra-high pressure device such as a girdle type or a belt type.
次に本発明の複合焼結体及びその製造方法全実施例に従
って評糺に説明する。Next, the composite sintered body of the present invention and its manufacturing method will be described in detail according to all embodiments.
実施例1
平均粒e3μmのCBNf60%と平均粒度3μmの(
40%’jl”1−40%W−15%’f’a=5%N
b)CD炭化物固溶体全20%と平均粒度1.5μmの
(T ’o、9−Tao、□)N ’ik 15%と9
00℃で熱処理した1 5 μm以下の79%kl 3
0%’l’1 m金粉末ff15%と全混合粉煙して外
径16i+i、高さ1.5gmに型押成形した。この粉
末圧粉体と同じく外径16Uの超硬合金の間に粉末圧粉
体の3%に相当するCO製薄板倉挾んでMo製容器内に
設置し、具空度1O−4關Hg、温度1000℃で脱ガ
スした後、ベルトm高圧装置に装入し圧力50Kb、温
度1450℃で20分間保持して破合焼結体金得た。こ
の複今焼結体全放電切断し、超硬合金の先端にロウ付け
して5NP432 テップに仕上けた。この本発明の複
合焼結体がロー付けされた5NP432 と市販のCB
N^圧焼結体がロー付けされた5NP432を比較にし
て下記の〜1続旋削条件によって切削し、欠損又はチッ
ピング迄の切削時間で4回比較測定した結果、本発明品
は、42分、45分、43分、47分であったのに対し
市販品は、13分、16分、20分、10分で、本発明
品が断続旋8υ試験における耐欠損性で後れており、し
かも繰υ返し同−試験全行った結果のバラツキ程度でも
本発明が優れている傾向にあることがa認できた。Example 1 CBNf60% with average grain e3μm and (with average grain size 3μm)
40%'jl''1-40%W-15%'f'a=5%N
b) (T'o, 9-Tao, □)N'ik 15% and 9 with a total of 20% CD carbide solid solution and an average particle size of 1.5 μm
79% kl 3 below 15 μm heat treated at 00℃
The entire mixture was mixed with 0%'l'1m gold powder ff15% and molded into an outer diameter of 16i+i and a height of 1.5gm. This powder compact was placed in a Mo container with a CO thin plate clamping the same amount as 3% of the powder compact between cemented carbide with an outer diameter of 16U, After degassing at a temperature of 1,000°C, it was charged into a belt m high-pressure device and maintained at a pressure of 50 Kb and a temperature of 1,450°C for 20 minutes to obtain a fractured sintered body. This composite sintered body was completely electrically discharged and soldered to the tip of the cemented carbide to give a 5NP432 tip. 5NP432 to which the composite sintered body of the present invention was brazed and commercially available CB
In comparison, 5NP432 to which the N^ pressure sintered body was brazed was cut under the following continuous turning conditions, and the cutting time until chipping or chipping was compared four times. The results were 45 minutes, 43 minutes, and 47 minutes, whereas the commercial products were 13 minutes, 16 minutes, 20 minutes, and 10 minutes, and the product of the present invention was behind in fracture resistance in the interrupted rotation 8υ test. It was confirmed that the present invention tends to be superior even in terms of variations in the results of all the repeated tests.
断続旋削条件
板r:J1j材 SCM−3(MRC58〜62ン
8mxrllのスロット金2本人れた50ψの断続旋削
切削jl裳 100m/min
切り込み 0.15XIl
送り速度 0.25111111/ rev本発明の複
合焼結体の内高纜度相菫化7/lit素焼結体の部分を
X線解析した結果、CBNと
(Ti、Ta)NCとTiB2と
(T i、 w、 T a、 Nb ) CNとAz3
TtCo と考えられるピークと析出したと考えられ
るWCのピークが確認できん、。又顕微鏡組織観察から
も析出しfcWCが確認できた。Intermittent turning condition plate r: J1j material SCM-3 (MRC58-62 inch 8mxrll 2 slotted 50ψ intermittent turning cutting JL 100m/min Depth of cut 0.15XIl Feed rate 0.25111111/rev Composite firing of the present invention As a result of X-ray analysis of the part of the high-strength phase violetized 7/lit elemental sintered body, CBN, (Ti, Ta) NC, TiB2, (Ti, w, Ta, Nb) CN, and Az3 were analyzed.
The peak thought to be TtCo and the peak of WC thought to be precipitated could not be confirmed. Furthermore, precipitated fcWC was confirmed by microscopic structure observation.
実施例2
平均粒度3μmのCBNi65%と平均粒度1.5μm
の(40%゛r i −50%W −10%Ta)Cの
炭化物固溶体を15%と平均粒度1.5μmの(’、I
’ t O,7Z r o、 3) N f 20%と
金混合粉伜して外径16朋、高さ1.5朋に型押成形し
た。この粉床圧粉体と同じく外径16朋の超硬合金の一
間にイオングレーティングによって圧粉体の3%に相当
する量のZr2蒸層し、この然層面に圧粉体の3%に相
当する量のN1製薄板を置き、このNi製薄板に圧粉体
を接触させてrA o製容器内に設置し、ベルト型高圧
装置に装入し圧力5oKb。Example 2 65% CBNi with an average particle size of 3 μm and an average particle size of 1.5 μm
A carbide solid solution of (40%゛r i -50%W -10%Ta)C with 15% and an average particle size of 1.5μm (',I
' t O,7Z r o, 3) 20% Nf and gold mixed powder were pressed and molded to have an outer diameter of 16 mm and a height of 1.5 mm. Like this powder bed compact, a Zr2 vapor layer with an amount equivalent to 3% of the compact is formed on the surface of this natural layer by ion grating on a piece of cemented carbide with an outer diameter of 16 mm. A corresponding amount of N1 thin plate was placed, a green compact was placed in contact with the Ni thin plate, and the compact was placed in a container made of rAo, which was then charged into a belt-type high-pressure device at a pressure of 5 kb.
温度1400 ’Cで20分間株持して仮台焼結体を得
た。これ全実施例1と同僚にして8NP 432 に仕
上は市販のC”BNN正圧焼結体ロー付けされた5NP
432 ’(r比較にして下記の旋削条件によって切削
し、平均逃げ面摩耗量を両足した結果本発明品は、平均
でV!l=0.13範に対し巾販品は平均でVB=0.
18題と不発ツJ品が耐摩耗性で浚れていることが確認
できた。しかも繰返し同−試験を行った結果のバラツキ
程匿でも本発明品がバラツキ範囲が狭く安>、ij、
していることが確認できた。A temporary sintered body was obtained by holding at a temperature of 1400'C for 20 minutes. This was all done with Example 1 and 8NP 432.The finish was 5NP with commercially available C"BNN positive pressure sintered body brazed.
432' (r Comparatively, cutting was performed under the following turning conditions, and the average flank wear amount was added up. The product of the present invention has an average of V!l = 0.13 range, whereas the product of the wide market has an average of VB = 0. ..
It was confirmed that 18 items and the unexploded J items were wear resistant and dredged. Moreover, even if the variation in the results of repeated identical tests is suppressed, the product of the present invention has a narrow variation range and is inexpensive.
I was able to confirm that it was.
旋削条件
被削材 5KI)−11HRC59〜62切削速度
9Qm/min
切り込み 0.5鵡
送 リ 0.1關/rev切削時間 2
0分
切削油 エマルカット &10
木兄ψ」の複@滉結体の内尚密度相屋化棚索焼結体の部
分全X線解析した結果、CBNと(Ti、Zr)NCと
Ni −Zrと
(Ti、W、 ’1” a ) CN と考えられるピ
ークと析出したと考えられるWCのピークが確認できた
。又、促〔1微鏡組織観察からも析出したvvCが確認
できた。Turning conditions Work material 5KI)-11HRC59~62 Cutting speed
9Qm/min Depth of cut 0.5mm Feed 0.1mm/rev Cutting time 2
0 minute cutting oil Emulcut (Ti, W, '1''a) A peak thought to be CN and a peak of WC thought to be precipitated were confirmed. Also, precipitated vvC was confirmed from microscopic structure observation.
実施例3
一′f−均粒度3μmのCBN全68%と平均粒度1.
5 μmの(55%’、1’1−35%W−10%Ta
)Cの炭化物固溶体10%と平均粒度145μmの(T
i o9−Nb、□)N ’c 15%と900℃で
熱処理しi15μm以下の70%Ti−30%8i 合
金粉末を7%とを混合粉砕して外径16mm、高さ1.
5朋に型理成形した。これをMO製容器内で外径16朋
、高さ3Bのwc−1ow量%colsi&合金の一面
に接触して設置献し、真空度10−4mmHg、温度1
000℃で脱カスした後、−ベルト型高圧装置に装入し
、昇温途中WC−Coの共晶点近辺で20分保持後更に
昇温して1400℃で20分医持して本発明の懐@戊給
体を得た。これ金夷酒輿」lと同僚にして5NP432
に仕上は市販のCB N高圧焼結体がロー付けされた8
NP432 を比較(−て下記の7ライス切削条件によ
って切削し、複合焼結体と#硬合金との固眉結合強夏も
含めた耐久傾注音調べた。試験の結果本発明の複合焼結
体は、5分切削後も正富摩耗であったのに対し、比較に
加えた市販の候合焼結体は3分切削後刃先欠損したもの
及びMi硬合金との固着結合部で欠損したものがあった
。Example 3 - Total 68% CBN with an average particle size of 3 μm and an average particle size of 1.
5 μm (55%', 1'1-35%W-10%Ta
) with a carbide solid solution of 10% and an average particle size of 145 μm (T
i o9-Nb, □) N'c 15% and 70% Ti-30%8i alloy powder heat-treated at 900°C and having an i of 15 μm or less were mixed and ground to form an outer diameter of 16 mm and a height of 1.
It was molded into 5 pieces. This was placed in contact with one surface of the wc-1ow% colsi & alloy with an outer diameter of 16mm and a height of 3B in an MO container, and the vacuum level was 10-4mmHg and the temperature was 1.
After removing the scum at 1,400°C, it was charged into a belt-type high-pressure device, held for 20 minutes near the eutectic point of WC-Co during heating, and then further heated to 1,400°C for 20 minutes to obtain the present invention. I got a bosom @ 戊supply body. This is 5NP432 as a co-worker with Kinyoshi Sakukoshi.
Finished with commercially available CBN high pressure sintered body 8
Comparing NP432 (-), the composite sintered body was cut under the following 7 rice cutting conditions, and the durability and tilting sound of the composite sintered body and # hard alloy, including the strength of the strong bond between them, were investigated.The test results showed that the composite sintered body of the present invention showed Masatomi wear even after 5 minutes of cutting, whereas the commercially available sintered compacts used for comparison showed chipping at the cutting edge after 3 minutes of cutting, and chipping at the bonded joint with the Mi hard alloy. there were.
フライス切削条件
被削材 5KDII HRC59〜6250X10
0の面を切削
切削速度 200m/mln
切り込み 1.0躇
送 リ 0.3朋/ rev切削切削試
験線X線マイクロアナライザーって調べた成木発明の複
@焼結体の商密度相屋イヒhm素焼紹捧部にはCOが滲
透拡散していること〃59認でき更にX腺解析と顕倣鏡
組織観際の結果析出した冑Cが確認できた〇
実施例4
平均粒度3μ■1のCf31〜と平均粒度5μmのWB
Nと第1表に示した平均粒度1〜3μmの炭化物固溶体
及び霊化物化合吻と全第1表に示した組成に配合し、実
施例2と同様の製造方法によって焼結した本発明の複合
焼結体の晶冨度相室イヒ硼素lj8結体部分=2X線解
析及びX紛マイクロアナライザーで調べた結果、各試料
共高折度相鼠イヒUIll素の他にBl型炭窒化物固溶
体とIll i、zr、i(f、Ta、Nb、Vの1種
以上の蟹化物又は窒炭化物もしくは相互同浴体化合物と
窒化アルミニウム、4a族遷移金属の硼化物又は硼屋化
物及び金属間化合物と判断出来るピークが確認でき、更
に各試料全てにVVCのピークが確認できた。各試料に
析出したWCについては顕微鏡組織観察からも再確認し
た。板状物体からの♂透拡散元素についてはX腺マイク
ロアナライザーによっても確認した。Milling cutting conditions Work material 5KDII HRC59~6250X10
Cutting 0 surface Cutting speed 200m/mln Depth of cut 1.0 feed Re 0.3/rev Cutting Cutting test line It was confirmed that CO permeated and diffused in the hm bisque fired part, and as a result of X-ray analysis and microscope microscopic examination, it was confirmed that precipitated C was present.Example 4 Average particle size of 3μ WB with Cf31 ~ and average particle size of 5 μm
The composite of the present invention was prepared by blending N, a carbide solid solution with an average particle size of 1 to 3 μm shown in Table 1, and a spirit compound compound in the composition shown in Table 1, and sintered by the same manufacturing method as in Example 2. As a result of examination using X-ray analysis and an X-powder microanalyzer, it was found that each sample contained a Bl-type carbonitride solid solution in addition to a high-order phase, a Bl-type carbonitride solid solution. i, zr, i (f, Ta, Nb, one or more nitrides or mutually homopolymer compounds, aluminum nitride, borides or borides of group 4a transition metals, and intermetallic compounds) In addition, the VVC peak was confirmed in all samples.The WC precipitated in each sample was also confirmed by microscopic structure observation.The male permeation diffusion elements from the plate-like object were confirmed using an X-gland microscopic microscope. This was also confirmed using an analyzer.
これら第1表に示した本発明の収容焼結体の内、試′4
+着号1.3.4.8.10と第2衣に示した本発明ケ
外れた被合焼結体の内、試料番号11.12をでれそれ
5NP432のチップに仕上けて更に市販のCBN糸焼
結体も比較に加えて実施例1と同様の切削粂往によって
切f9υ試験全行ない、その結果金弟3衣3Cボした。Among the contained sintered bodies of the present invention shown in Table 1, sample '4
+ Among the sintered bodies shown in No. 1.3.4.8.10 and No. 2, which were removed from the present invention, sample No. 11.12 was finished into a 5NP432 chip and further commercialized. In addition to comparison, the CBN yarn sintered body was also subjected to a cutting f9υ test in the same manner as in Example 1, and as a result, it was found to be 3C.
第3表
第3表の結果、本発明の複合焼結体は、断続旋削試験に
セける耐欠損性が従来の市販されている複合焼結体に比
較して著しく後れていることが確認できた。Table 3 The results shown in Table 3 confirm that the composite sintered body of the present invention is significantly inferior in fracture resistance in the interrupted turning test compared to conventional commercially available composite sintered bodies. did it.
実施例5
実施例4の第1表に示した試料番号5.6.70本発明
の複合焼結体と第2表に示した試料番号13.14の本
発明から外れた複合焼結体と市販のCBN糸焼結体全比
較に加えて下記の条件で大越式摩耗試験を行った。この
結果、本発明の複合焼結体である試料5,6.7の摩れ
量は、本発明から外れた複合焼結体である試料番号13
.14及び市販のCBN系焼結体に比較して約1/2で
あった。Example 5 Composite sintered body of the present invention with sample number 5.6.70 shown in Table 1 of Example 4 and composite sintered body of the present invention with sample number 13.14 shown in Table 2 In addition to comparing all commercially available CBN yarn sintered bodies, an Okoshi type abrasion test was conducted under the following conditions. As a result, the amount of wear of samples 5 and 6.7, which are composite sintered bodies of the present invention, is different from that of sample number 13, which is a composite sintered body of the present invention.
.. It was about 1/2 compared to No. 14 and commercially available CBN-based sintered bodies.
太總式摩耗試験粂件
ローター摩擦速度 195 m/mi n初期加圧
4縁
4史終力]1月二 19.5
Kf輩源時間 1時間Taisho type wear test Rotor friction speed 195 m/min Initial pressure 4 edges 4 history Final force] January 2 19.5
Kf haigen time 1 hour
第1図は、WCとIll i CとTaCの3X分糸状
態図を示す。FIG. 1 shows a 3X phase diagram of WC, Ill i C, and TaC.
Claims (1)
と20〜600〜60捧槓チと不可避不純物から成る焼
結体と超硬合金又はサーメットとが強固にfi!II層
した俵合体において、前記焼結体の結合相が焼結体の体
積比で2〜40%の(’1’ i、 W、 ’l” a
)CN又は(’l’ i 、 W、 T a、 N b
) CI’lJのBl型固溶体と6〜40%のT i、
Zr、 Hf、 ’i’a、 Nb、 Vの1棟以上
の窒化物、炭窒化物もしくはこれらの相互固溶体化合物
と1〜20%のAL、 Si、 T i、 ′l!r。 Hf、 k’e、 Ni、 Coの2a以上から成る金
属間化合物および/またはAt、 S i、 ’、I’
i、 Zr、 Hf。 l″e、Ni、Coの1種以上の硼化物、硼屋化物もし
くはこれらの相互固溶体化合物と0.1〜20%の粒界
析出したWC−f含有してiること全特徴とする複合焼
結体。 (2) 出発原料として40〜800〜80捧槓チ
および/またはWBN と2〜40捧槓チの第1図に
表わすA、B、C,Dの線上及び各点内にあるBl型炭
化物固固溶体但し、TaCに対して30%以下はNbC
で置換可ンと6〜40体積%のTi5Z r、 Hf、
T a、 Nb%V (7)1 檎以上02化物モ
しくはこれらの相互固溶体化合と1〜20坏槙%ノAz
、 S i、f1、Zr、Hfの1i以上ノ金属又は合
金とを混合粉砕後成形した粉末圧粉体音)”e、Nj、
Coの1榴以上の金属又は合金を含有し7′C,超硬台
金又はサーメットに@接接触させて超簡圧高温トで21
12i結し、CBNおよび/またはWBN負4!焼結体
内に前記BI型炭化物固浴体から0.1〜20捧槓チの
WC<粒界析出させると共に前記超硬合金又はサーメッ
トから上’e、Nj、Coの18i以上の金属又は合金
全滲透拡散させて超硬合金又はサーメットと強固に固着
M曾させたこと全特徴とする複合焼結体の製造方法。 (3)出発原料として40〜80体積−〇〇BNおよび
/またはWBNと2〜40捧槓チの第1図に表わすA、
B、C,Dの蔵上及び谷点内にめるB1型炭化物固溶体
(但し、TaCに対して30%以下はNbCで置換町)
と6〜40体積−〇″r!、Zr、 Hf、 Ta、
Nb、 V の1槙以上の窒化物もしくはこれらの相
互固溶体窒化物と全混合粉砕後成形した粉末圧粉体と該
粉末圧粉体の一面にAt、Sl、Tj、 Zr、、Hf
、 Fe、 Ni、 Co の1棟以上の金属又は合
金から成る板状物体全接触させ、成板状物体の他面又は
前記粉末圧粉体の他面に超硬合金又はサーメット全装p
!!i設置して超爾圧高温下で焼結し、CBNおよび/
またはWBN含M焼結体内に前記Bl型炭化物固溶体か
ら0.1〜20体積チのWC2粒界析出させると共に前
記板状物体から滲透拡敵させて1〜20#積チのA t
、 S s、’l’i、 Zr、 Hf、 Fe、 N
i、 Coの2種以上から成る金属間化合物および/ま
たはkt、 S i、 T i。 Zr、 Hf、 Fe、 Ni、 Co の1柚以上
の硼化物、#l輩化物もしくはこれらの相互固溶体化合
物全存在させて超硬合金又はサーメットと強固に回漕結
付させたことを特徴とする複合焼結体の製造方法。[Claims] (1140 to 80 volumes of CBN and/or WBN
The sintered body consisting of 20~600~60 molten metal and unavoidable impurities and the cemented carbide or cermet are strongly fi! In the II layered bale combination, the binder phase of the sintered body has a volume ratio of 2 to 40% ('1' i, W, 'l' a
) CN or ('l' i, W, T a, N b
) Bl-type solid solution of CI'lJ and 6-40% Ti,
One or more nitrides, carbonitrides, or mutual solid solution compounds of Zr, Hf, 'i'a, Nb, V and 1 to 20% of AL, Si, Ti, 'l! r. Intermetallic compound consisting of 2a or more of Hf, k'e, Ni, Co and/or At, Si, ', I'
i, Zr, Hf. A composite containing one or more borides, borides, or mutual solid solution compounds of 1''e, Ni, and Co, and 0.1 to 20% of WC-f precipitated at grain boundaries. Sintered body. (2) 40 to 800 to 80 pieces as starting material
and/or WBN and Bl-type carbide solid solution on the lines A, B, C, and D shown in Figure 1 and within each point of the 2 to 40 strips.However, 30% or less of TaC is NbC.
6 to 40 volume % of Ti5Z r, Hf,
Ta, Nb%V (7) 1 to 20 compounds or their mutual solid solution combination and 1 to 20% of NbAz
, S i, f1, Zr, Hf, 1i or more metals or alloys are mixed and pulverized and then compacted)"e, Nj,
Containing a metal or alloy of 1 or more Co, 7'C, in contact with a carbide base metal or cermet, and heated under ultra-simple pressure at high temperature to 21
12i, CBN and/or WBN negative 4! In the sintered body, 0.1 to 20 g of WC is precipitated from the BI type carbide solid bath at the grain boundaries, and all metals or alloys of 18i or more of upper 'e, Nj, and Co are precipitated from the cemented carbide or cermet. A method for manufacturing a composite sintered body, which is characterized in that it is firmly fixed to a cemented carbide or cermet by permeation diffusion. (3) A shown in Figure 1 with 40 to 80 volumes of BN and/or WBN and 2 to 40 volumes as starting materials,
B1 type carbide solid solution placed above and within the valleys of B, C, and D (however, 30% or less of TaC is replaced with NbC)
and 6~40 volume-〇″r!, Zr, Hf, Ta,
One or more nitrides of Nb, V or their mutual solid solution nitrides and a powder compact formed after pulverization, and At, Sl, Tj, Zr, , Hf on one side of the powder compact.
, Fe, Ni, Co, all of which are made of a plate-like object made of one or more metals or alloys, and the other surface of the plate-like object or the other surface of the powder compact is completely covered with cemented carbide or cermet.
! ! i and sintered under ultra-high pressure and high temperature to form CBN and/or
Alternatively, 0.1 to 20 volumes of WC2 grain boundaries are precipitated from the Bl type carbide solid solution in the WBN-containing M sintered body, and A t of 1 to 20 volumes is permeated from the plate-like object.
, S s, 'l'i, Zr, Hf, Fe, N
i, an intermetallic compound consisting of two or more of Co, and/or kt, S i, Ti. A composite characterized by the presence of one or more borides of Zr, Hf, Fe, Ni, Co, #l oxides, or mutual solid solution compounds thereof, which are strongly bonded to cemented carbide or cermet. A method for producing a sintered body.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP20713982A JPS5997579A (en) | 1982-11-26 | 1982-11-26 | Composite sintered body and manufacture |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP20713982A JPS5997579A (en) | 1982-11-26 | 1982-11-26 | Composite sintered body and manufacture |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS5997579A true JPS5997579A (en) | 1984-06-05 |
| JPH0254300B2 JPH0254300B2 (en) | 1990-11-21 |
Family
ID=16534841
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP20713982A Granted JPS5997579A (en) | 1982-11-26 | 1982-11-26 | Composite sintered body and manufacture |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS5997579A (en) |
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5041399A (en) * | 1989-03-07 | 1991-08-20 | Sumitomo Electric Industries, Ltd. | Hard sintered body for tools |
| US5092920A (en) * | 1988-12-14 | 1992-03-03 | Sumitomo Electric Industries, Ltd. | Sintered body for high-accuracy working tools |
| US20120114437A1 (en) * | 2009-06-01 | 2012-05-10 | Seco Tools Ab | Nanolaminated coated cutting tool |
-
1982
- 1982-11-26 JP JP20713982A patent/JPS5997579A/en active Granted
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5092920A (en) * | 1988-12-14 | 1992-03-03 | Sumitomo Electric Industries, Ltd. | Sintered body for high-accuracy working tools |
| US5041399A (en) * | 1989-03-07 | 1991-08-20 | Sumitomo Electric Industries, Ltd. | Hard sintered body for tools |
| US20120114437A1 (en) * | 2009-06-01 | 2012-05-10 | Seco Tools Ab | Nanolaminated coated cutting tool |
| US8864861B2 (en) * | 2009-06-01 | 2014-10-21 | Seco Tools Ab | Nanolaminated coated cutting tool |
Also Published As
| Publication number | Publication date |
|---|---|
| JPH0254300B2 (en) | 1990-11-21 |
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