JPH0369860B2 - - Google Patents
Info
- Publication number
- JPH0369860B2 JPH0369860B2 JP3234985A JP3234985A JPH0369860B2 JP H0369860 B2 JPH0369860 B2 JP H0369860B2 JP 3234985 A JP3234985 A JP 3234985A JP 3234985 A JP3234985 A JP 3234985A JP H0369860 B2 JPH0369860 B2 JP H0369860B2
- Authority
- JP
- Japan
- Prior art keywords
- diamond
- joining
- based sintered
- sintered material
- members
- 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.)
- Expired
Links
- 229910003460 diamond Inorganic materials 0.000 claims description 30
- 239000010432 diamond Substances 0.000 claims description 30
- 239000000463 material Substances 0.000 claims description 29
- 238000005304 joining Methods 0.000 claims description 25
- 238000005219 brazing Methods 0.000 claims description 21
- 229910052751 metal Inorganic materials 0.000 claims description 20
- 239000002184 metal Substances 0.000 claims description 20
- 239000000945 filler Substances 0.000 claims description 19
- 238000000034 method Methods 0.000 claims description 17
- 239000000203 mixture Substances 0.000 claims description 14
- 239000011230 binding agent Substances 0.000 claims description 9
- 238000010438 heat treatment Methods 0.000 claims description 7
- UONOETXJSWQNOL-UHFFFAOYSA-N tungsten carbide Chemical compound [W+]#[C-] UONOETXJSWQNOL-UHFFFAOYSA-N 0.000 claims description 6
- 229910052799 carbon Inorganic materials 0.000 claims description 4
- 239000000843 powder Substances 0.000 description 14
- 239000012071 phase Substances 0.000 description 8
- 230000000694 effects Effects 0.000 description 6
- 238000004519 manufacturing process Methods 0.000 description 6
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 5
- 229910052796 boron Inorganic materials 0.000 description 5
- 230000000052 comparative effect Effects 0.000 description 5
- 238000005520 cutting process Methods 0.000 description 5
- 238000005245 sintering Methods 0.000 description 3
- 229910020674 Co—B Inorganic materials 0.000 description 2
- 239000000853 adhesive Substances 0.000 description 2
- 230000001070 adhesive effect Effects 0.000 description 2
- 229910045601 alloy Inorganic materials 0.000 description 2
- 239000000956 alloy Substances 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 238000000576 coating method Methods 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 239000000470 constituent Substances 0.000 description 2
- 238000009792 diffusion process Methods 0.000 description 2
- 238000002844 melting Methods 0.000 description 2
- 230000008018 melting Effects 0.000 description 2
- 239000002245 particle Substances 0.000 description 2
- 229910000521 B alloy Inorganic materials 0.000 description 1
- ZOXJGFHDIHLPTG-UHFFFAOYSA-N Boron Chemical compound [B] ZOXJGFHDIHLPTG-UHFFFAOYSA-N 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- 229910002804 graphite Inorganic materials 0.000 description 1
- 239000010439 graphite Substances 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 239000007791 liquid phase Substances 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 229910052755 nonmetal Inorganic materials 0.000 description 1
- 150000002843 nonmetals Chemical class 0.000 description 1
- 230000001590 oxidative effect Effects 0.000 description 1
- 238000007747 plating Methods 0.000 description 1
- 238000003466 welding Methods 0.000 description 1
Landscapes
- Pressure Welding/Diffusion-Bonding (AREA)
- Ceramic Products (AREA)
Description
〔産業上の利用分野〕
この発明は、ダイヤモンド基焼結材料部材を高
い接合強度で炭化タングステン基超硬合金部材
(以下、単に超硬合金部材という)に接合する方
法に関するものである。
〔従来の技術〕
一般に、ダイヤモンド基焼結材料は、結合相形
成成分として少なくともCo粉末およびNi粉末の
いずれか、または両方を配合し、残りの主要部が
ダイヤモンド粉末からなる混合粉末を、5万気圧
以上の超高圧下で、約1400℃の高温に加熱して焼
結することによつて製造されるものであり、高硬
度とすぐれた耐摩耗性を有することから、主とし
て非金属や非鉄金属などの切削に切削工具として
用いられている。
この場合、上記のダイヤモンド基焼結材料部材
は、通常同じく結合相形成成分としてCoおよび
Niのいずれか、または両方を含有し、残りの主
要部が炭化タングステン(以下WCで示す)から
なる組成を有する超硬合金部材に接合させた状態
で実用に供されているが、これら両部材は、ろう
付けなどの通常の手段では接合することがきわめ
て困難であることから、前記のダイヤモンド基焼
結材料の焼結時に、前記の超硬合金部材をこれと
一緒に挿入して、焼結と同時に接合を行なつてい
るのが現状である。
〔発明が解決しようとする問題点〕
このようにダイヤモンド基焼結材料部材と超硬
合金部材の接合は、前記ダイヤモンド基焼結材料
の焼結と同時に行なわれるものであるため、前記
超硬合金部材の占める分だけダイヤモンド基焼結
材料の生産割合が少なくなり、これがコスト高の
原因となつている。
したがつて、ダイヤモンド基焼結材料の製造に
際して用いられているような超高圧を用いること
なく、かつダイヤモンド基焼結材料の焼結とは別
個に、ダイヤモンド基焼結材料部材を超硬合金部
材に接合することができれば、従来一緒に挿入さ
れていた超硬合金部材の分だけダイヤモンド基焼
結材料の生産割合が増すことになつて、その分だ
けコスト低減をはかることができるようになる。
さらに、上記のように通常の接合手段ではダイ
ヤモンド基焼結材料部材を超硬合金部材に接合す
ることは困難であるから、例えば超硬合金製切刃
の刃先に極小のダイヤモンド基焼結材料を接合し
た構造の切削工具を製造することは困難である
が、超高圧を用いないで、これら両部材を接合す
ることができれば、前記切削工具の製造もきわめ
て容易となる。
〔問題点を解決するための手段〕
そこで、本発明者等は、上述のような観点か
ら、超高圧を用いずに、上記のダイヤモンド基焼
結材料部材を超硬合金部材に結合すべく研究を行
なつた結果、前記両部材の接合面に、少なくとも
B(ほう素):3〜20原子%を含有し、さらに必要
に応じてC(炭素):1〜10原子%を含有し、残り
の主要部がCoおよびNiのいずれか、または両方
からなる配合組成あるいは成分組成を有するろう
材を介在させた状態で、これら両部材を、30Kg/
cm2以上、実用的には30〜300Kg/cm2の圧力を付加
しながら、750〜900℃の温度に加熱すると、この
ろう材中のB成分、あるいはB成分とC成分が前
記両部材の結合相内に拡散することから、前記両
部材の結合相と前記ろう材とが一体化するように
なり、この結果前記両部材はきわめて高い接合強
度、すなわち20Kg/mm2以上の高い剪断強度で接合
されるようになるという知見を得たのである。
この発明は、上記知見にもとづいてなされたも
のであつて、結合相形成成分としてCoおよびNi
のいずれか、または両方を含有するダイヤモンド
基焼結材料部材を、同じく結合相形成成分として
CoおよびNiのいずれか、または両方を含有する
超硬合金部材に接合するに際して、これら両部材
の接合面に、少なくともB:3〜20原子%を含有
し、さらに必要に応じてC:1〜10原子%を含有
し、残りの主要部がCoおよびNiのいずれか、ま
たは両方からなる配合組成あるいは成分組成を有
するろう材を介在させた状態で、これら両部材
を、30Kg/cm2以上、実用的には30〜300Kg/cm2の
圧力を付加しながら、750〜900℃の範囲内の所定
温度に加熱して、前記ろう材中のB成分、さらに
必要に応じてC成分を前記両部材内へ拡散させる
ことによつて前記両部材の強固な接合をはかつた
点に特徴を有するものである。
つぎに、この発明の接合方法において、その条
件を上記の通りに限定した理由を説明する。
(a) ろう材中のB含有量
B成分には、ろう材の融点を低下させて、接合
加熱温度である750〜900℃の温度で液相を形成
し、自身は加圧状態で、いずれも接合部材の結合
相の主要構成成分であるCoおよび/またはNi中
に拡散して、これら部材を一体化し、もつて強固
な接合をはかる作用があるが、その含有量が3原
子%未満では前記作用に所望の効果が得られず、
一方20原子%を越えて含有させると、両部材の接
合面にかなりの量のB成分が残留するようにな
り、このB成分は接合部材の結合相形成成分およ
びろう材構成成分と脆い化合物を形成し、この化
合物が多量に形成されると接合面の接合強度が著
しく低下するようになることから、その含有量を
3〜20原子%と定めた。
(b) ろう材中のC含有量
C成分は、B成分と共存した状態で、ろう材の
融点を一段と低下させ、ろう材を低温側で液相化
する作用をもつので、相対的に低い接合加熱温度
が要求される場合に必要に応じて配合あるいは含
有されるが、その含有量が1原子%未満では前記
作用に所望の効果が得られず、一方10原子%を越
えて含有させると、接合面に遊離炭素として残留
するようになつて、接合強度が低下するようにな
ることから、その含有量を1〜10原子%と定め
た。
(c) 接合加熱温度
750℃未満の接合加熱温度では、B成分の接合
部材への拡散速度が低く、この結果接合面に多量
のB成分が残留するようになつて、高い接合強度
を得ることができず、一方900℃を越えた接合加
熱温度にすると、特にダイヤモンド基焼結材料部
材に変質が起つて、高い接合強度は得られるもの
の、切削性能の劣化を招くようになることから、
その温度を750〜900℃と定めた。
(d) 付加圧力
接合に際して、接合部材の接合面に、接合強度
低下の原因となる空隙が形成されるのを防止する
ために圧力が付加されるが、付加圧力が30Kg/cm2
未満では完全に空隙発生を防止することができな
いので、30Kg/cm2以上の圧力を付加して空隙のな
い均一な接合面を得るようにする必要がある。な
お、付加圧力が高いほど接合強度は高くなるが、
実用的には30〜300Kg/cm2の付加圧力で十分満足
する接合強度を得ることができる。
なお、この発明の接合方法を実施するに当つ
て、ろう材は、それぞれ平滑に研削した接合面
に、メツキ法あるいは粉末塗布法などの方法によ
つて適用するのがよく、また、両部材の接合は、
雰囲気制御が可能なホツトプレス機を用い、非酸
化性ガス雰囲気中あるいは真空中で行なうのが好
ましく、密閉容器内での実施が可能ならば、雰囲
気は大気でもよい。
〔実施例〕
つぎに、この発明の接合方法を実施例により具
体的に説明する。
実施例 1
接合部材として、直径:7mmφ×厚さ:1mmの
寸法をもち、かつ第1表に示される成分組成をも
つたダイヤモンド基焼結材料部材と、直径:7mm
φ×厚さ:6mmの寸法をもち、かつ同じく第1表
に示される成分組成をもつた超硬合金部材を用意
した。
一方、ろう材形成粉末として、平均粒径:1.2μ
mを有するCo粉末、同1.8μmのCo−B合金
(B:30原子%含有)粉末、および同0.5μmの炭
素粉末を用意し、これら粉末をそれぞれ第1表に
示される配合組成に配合し、これに有機接着剤を
加えて混合してペースト状とし、これらのペース
トを、上記接合部材のそれぞれの接合面に、5μ
mの平均厚さで塗布した後、これらの両部材を接
合面で重ね合わせた状態で、ホツトプレ
[Industrial Application Field] The present invention relates to a method for joining a diamond-based sintered material member to a tungsten carbide-based cemented carbide member (hereinafter simply referred to as a cemented carbide member) with high bonding strength. [Prior Art] In general, diamond-based sintered materials are produced by blending at least one of Co powder and Ni powder, or both, as a binder phase forming component, with the remaining main portion being diamond powder. It is manufactured by heating and sintering at a high temperature of approximately 1400℃ under ultra-high pressure above atmospheric pressure, and because it has high hardness and excellent wear resistance, it is mainly used for nonmetals and nonferrous metals. It is used as a cutting tool for cutting etc. In this case, the above-mentioned diamond-based sintered material member usually contains Co and Co as binder phase forming components.
It is put into practical use in a state where it is joined to a cemented carbide member containing one or both of Ni and the remaining main part is tungsten carbide (hereinafter referred to as WC). Since it is extremely difficult to join by normal means such as brazing, the cemented carbide member is inserted together with the diamond-based sintered material when the diamond-based sintered material is sintered. Currently, bonding is performed at the same time. [Problems to be Solved by the Invention] As described above, since the joining of the diamond-based sintered material member and the cemented carbide member is performed simultaneously with the sintering of the diamond-based sintered material, the cemented carbide The production ratio of diamond-based sintered material decreases as the number of parts occupies, and this becomes a cause of high costs. Therefore, a diamond-based sintered material member can be processed into a cemented carbide member without using ultra-high pressure as is used in the production of diamond-based sintered material, and separately from sintering of the diamond-based sintered material. If it can be joined to the diamond-based sintered material, the production rate of diamond-based sintered material will increase by the amount of the cemented carbide component that was conventionally inserted together, and it will be possible to reduce costs by that amount. Furthermore, as mentioned above, it is difficult to join a diamond-based sintered material member to a cemented carbide member using normal joining means. It is difficult to manufacture a cutting tool with a joined structure, but if these two members can be joined without using ultra-high pressure, manufacturing the cutting tool will be extremely easy. [Means for solving the problem] Therefore, from the above-mentioned viewpoint, the present inventors conducted research to bond the above-mentioned diamond-based sintered material member to a cemented carbide member without using ultra-high pressure. As a result, the bonding surface of both members contained at least 3 to 20 atom % of B (boron), and further contained 1 to 10 atom % of C (carbon) as necessary, and the remaining Both parts were weighed at 30 kg/100 lbs. with a brazing filler metal having a composition or component composition mainly consisting of Co and/or Ni.
When heated to a temperature of 750 to 900°C while applying a pressure of 30 to 300 kg/cm 2 or more , the B component or B and C components in the brazing filler metal are As it diffuses into the binder phase, the binder phase of the two components and the brazing filler metal become integrated, and as a result, the two components have an extremely high bonding strength, that is, a high shear strength of 20 kg/mm 2 or more. They found that they can be bonded together. This invention was made based on the above knowledge, and it is based on the above findings that Co and Ni are used as bonding phase forming components.
A diamond-based sintered material member containing one or both of the following is also used as a binder phase forming component.
When bonding to a cemented carbide member containing either or both of Co and Ni, the bonding surfaces of these two members contain at least 3 to 20 atomic percent of B, and if necessary, 1 to 20 atomic percent of C. 30 Kg/cm 2 or more, with a brazing filler metal containing 10 atomic % and the remaining main part consisting of Co and/or Ni, Practically speaking, the B component in the brazing filler metal and, if necessary, the C component are heated to a predetermined temperature within the range of 750 to 900°C while applying a pressure of 30 to 300 Kg/cm 2 . The feature is that the two members are firmly bonded by diffusing into the members. Next, the reason for limiting the conditions as described above in the joining method of the present invention will be explained. (a) B content in the brazing filler metal The B component lowers the melting point of the brazing filler metal, forms a liquid phase at a temperature of 750 to 900°C, which is the bonding heating temperature, and is itself in a pressurized state. It also diffuses into Co and/or Ni, which are the main constituents of the binder phase of bonding components, and has the effect of integrating these components and ensuring a strong bond, but if the content is less than 3 at%, The desired effect is not obtained from the action,
On the other hand, if the content exceeds 20 atom%, a considerable amount of the B component will remain on the joint surfaces of both parts, and this B component will form a brittle compound with the binder phase forming components and brazing material components of the joint parts. If a large amount of this compound is formed, the bonding strength of the bonded surface will be significantly reduced, so its content was determined to be 3 to 20 atomic percent. (b) C content in the brazing filler metal The C content is relatively low as it coexists with the B component and has the effect of further lowering the melting point of the brazing filler metal and causing the brazing filler metal to become liquid at low temperatures. It is blended or included as necessary when a bonding heating temperature is required, but if the content is less than 1 atomic %, the desired effect cannot be obtained, whereas if it is contained in excess of 10 atomic %, The content was determined to be 1 to 10 atomic % because free carbon remains on the bonding surface and reduces the bonding strength. (c) Bonding heating temperature At a bonding heating temperature of less than 750°C, the diffusion rate of the B component into the bonding members is low, and as a result, a large amount of the B component remains on the bonding surface, making it difficult to obtain high bonding strength. On the other hand, if the welding heating temperature exceeds 900°C, deterioration occurs especially in the diamond-based sintered material parts, and although high joint strength can be obtained, cutting performance deteriorates.
The temperature was set at 750-900℃. (d) Additional pressure During joining, pressure is applied to the joining surfaces of the joining members to prevent the formation of voids that will cause a reduction in joint strength, but the added pressure is 30Kg/cm 2
Since it is not possible to completely prevent the generation of voids if the pressure is less than 30 kg/cm 2 , it is necessary to apply a pressure of 30 Kg/cm 2 or more to obtain a uniform joint surface without voids. Note that the higher the applied pressure, the higher the bonding strength;
Practically, sufficient bonding strength can be obtained with an additional pressure of 30 to 300 kg/cm 2 . In carrying out the joining method of the present invention, it is preferable that the brazing filler metal is applied to the joint surfaces that have been ground smooth by a plating method or a powder coating method. The joining is
It is preferable to use a hot press machine capable of controlling the atmosphere in a non-oxidizing gas atmosphere or in a vacuum, and the atmosphere may be air if it can be carried out in a closed container. [Example] Next, the joining method of the present invention will be specifically explained with reference to Examples. Example 1 As a joining member, a diamond-based sintered material member having dimensions of diameter: 7 mmφ x thickness: 1 mm and having the composition shown in Table 1, and a diamond-based sintered material member with a diameter of 7 mm.
A cemented carbide member having dimensions of φ×thickness: 6 mm and having the same composition as shown in Table 1 was prepared. On the other hand, as a brazing filler metal forming powder, average particle size: 1.2μ
A Co powder having a diameter of 1.8 μm, a Co-B alloy (containing 30 at% B) powder having a diameter of 1.8 μm, and a carbon powder having a diameter of 0.5 μm were prepared, and these powders were blended into the composition shown in Table 1. Add an organic adhesive to this and mix to form a paste, and apply this paste to each bonding surface of the above bonding member in a layer of 5 μm.
After applying the coating to an average thickness of
【表】【table】
【表】
ス機の内径:7mmφを有するモールド内に挿入
し、同じく第1表に示される条件で接合を行なう
ことによつて、本発明接合法1〜11および比較接
合法1〜4をそれぞれ実施した。
なお、比較接合法1〜4は、いずれもろう材の
配合組成および接合条件のうちのいずれかの条件
(※印を付したもの)がこの発明の範囲から外れ
た条件で行なつたものである。
つぎに、この結果得られた接合部材の接合面の
剪断強度を測定すると共に、接合面の状況を観察
した。これらの測定および観察結果を第1表に合
せて示した。
実施例 2
接合部材として、直径:6mmφ×厚さ:1.2mm
の寸法をもち、かつ第2表に示される成分組成を
有するダイヤモンド基焼結材料部材と、直径:6
mmφ×厚さ:4mmの寸法を有し、同じく第2表に
示される成分組成をもつた超硬合金部材を用意し
た。
一方、ろう材形成粉末として、平均粒径:1.5μ
mを有するNi−B合金(B:20原子%含有)粉
末、同1.8μmのCo−B合金(B:30原子%含有)
粉末、同1.2μmのCo粉末、同1.5μmのNi粉末、
および0.5μmの炭素粉末を用意し、これら粉末を
第2表に示される配合組成に配合し、これに有機
接着剤を加えて混合してペースト状とし、これら
のペーストを、前記ダイヤモンド基焼結材料部材
の接合面に8μmの平均厚さで塗布し、ついで、
このように調製したダイヤモンド基焼結部材を接
合面同志が接触した状態で上記超硬合金部材に重
ね合わせ、これを上下の黒鉛パンチで加圧する形
式のホツトプレス機の内径:6mmφを有するキヤ
ビテイ内に挿入し、同じく第2表に示される条件
で接合を行なうことによつて本発明接合法12〜22
および比較接合法5〜8をそれぞれ実施した。
なお、比較接合法5〜8は、いずれも実施例1
におけると同様に、いずれかの条件がこの発明の
範囲から外れた条件で行なつたものである。
これらについても、実施例1におけると同様に[Table] Invention joining methods 1 to 11 and comparative joining methods 1 to 4 were performed by inserting the mold into a mold having an inner diameter of 7 mmφ and performing joining under the same conditions shown in Table 1. carried out. Note that Comparative Bonding Methods 1 to 4 were all carried out under conditions in which the composition of the brazing filler metal and the bonding conditions (marked with *) were outside the scope of the present invention. be. Next, the shear strength of the bonded surfaces of the resulting bonded members was measured, and the condition of the bonded surfaces was observed. The results of these measurements and observations are shown in Table 1. Example 2 As a joining member, diameter: 6 mmφ x thickness: 1.2 mm
A diamond-based sintered material member having the dimensions and the composition shown in Table 2, and a diameter: 6
A cemented carbide member having dimensions of mmφ×thickness: 4 mm and having the same composition shown in Table 2 was prepared. On the other hand, as a brazing filler metal forming powder, average particle size: 1.5μ
Ni-B alloy (containing 20 at% B) powder with m, Co-B alloy (containing 30 at% B) with the same 1.8 μm
powder, 1.2 μm Co powder, 1.5 μm Ni powder,
and 0.5 μm carbon powder, these powders were blended into the composition shown in Table 2, an organic adhesive was added and mixed to form a paste, and these pastes were mixed with the diamond-based sintered Apply it to the joint surface of the material parts at an average thickness of 8 μm, and then
The diamond-based sintered member thus prepared was stacked on the cemented carbide member with their joint surfaces in contact with each other, and then placed in a cavity with an inner diameter of 6 mmφ in a hot press machine that pressurized it with upper and lower graphite punches. The bonding methods 12 to 22 of the present invention can be obtained by inserting and bonding under the conditions shown in Table 2.
and comparative joining methods 5 to 8 were carried out, respectively. In addition, comparative joining methods 5 to 8 are all based on Example 1.
As in , some of the conditions were outside the scope of the present invention. Regarding these, as in Example 1,
【表】
接合面の剪断強度を測定し、かつ接合面状況を観
察し、その結果を第2表に示した。
また、本発明接合法12,13、および14につい
て、得られた接合部材の接合面におけるBおよび
Niの最大拡散深さを、それぞれXMA(X線マイ
クロアナライザー)により測定したところ、第3
表に示される結果を示した。[Table] The shear strength of the bonded surfaces was measured and the condition of the bonded surfaces was observed, and the results are shown in Table 2. In addition, for the bonding methods 12, 13, and 14 of the present invention, B and
When the maximum diffusion depth of Ni was measured using an XMA (X-ray microanalyzer), the third
The results are shown in the table.
第1〜3表に示される結果から明らかなよう
に、本発明接合法によれば、ろう材構成成分の接
合部材への拡散が十分に行なわれ、接合面に空隙
などの発生なく、良好な接合状態で、しかも20
Kg/mm2以上の高い剪断強度で強固にダイヤモンド
基焼結材料部材を超硬合金部材に接合することが
できるのに対して、比較接合法1〜8に見られる
ように、ろう材の成分組成および接合条件のうち
のいずれかの条件でもこの発明の範囲から外れる
と、接合状態が悪く、かつ接合面の剪断強度も20
Kg/mm2以下と低く、高い接合強度での接合が不可
能であることがわかる。
上述のように、この発明の接合方法によれば、
ダイヤモンド基焼結材料部材を超硬合金部材に、
超高圧を用いることなく、強固に接合することが
できるので、ダイヤモンド基焼結材料の製造コス
トの低減や、その使用分野の著しい拡大をはかれ
るなど工業上有用な効果がもたらされるのであ
る。
As is clear from the results shown in Tables 1 to 3, according to the joining method of the present invention, the constituent components of the brazing filler metal are sufficiently diffused into the joining members, and there is no formation of voids on the joining surfaces, resulting in good results. In the bonded state, and 20
While diamond-based sintered material parts can be firmly joined to cemented carbide parts with high shear strength of Kg/ mm2 or more, as seen in comparative joining methods 1 to 8, the composition of the brazing filler metal If any of the composition and bonding conditions are outside the scope of this invention, the bonding condition will be poor and the shear strength of the bonded surface will be 20%.
It can be seen that the bonding strength is as low as Kg/mm 2 or less, making it impossible to bond with high bonding strength. As mentioned above, according to the joining method of the present invention,
Diamond-based sintered material parts to cemented carbide parts,
Since it is possible to bond firmly without using ultra-high pressure, it brings about industrially useful effects such as reducing the manufacturing cost of diamond-based sintered materials and significantly expanding the field of use thereof.
Claims (1)
か、または両方を含有するダイヤモンド基焼結材
料部材を、同じく結合相形成成分としてCoおよ
びNiのいずれか、または両方を含有する炭化タ
ングステン基超硬合金部材に接合するに際して、
これら両部材の接合面に、少なくともB:3〜20
原子%を含有し、残りの主要部がCoおよびNiの
いずれか、または両方からなる配合組成あるいは
成分組成を有するろう材を介在させた状態で、こ
れら両部材を、30Kg/cm2以上の圧力を付加しなが
ら、750〜900℃の範囲内の所定温度に加熱して、
前記ろう材中のB成分を前記両部材内へ拡散する
ことを特徴とするダイヤモンド基焼結材料部材を
炭化タングステン基超硬合金部材に接合する方
法。 2 結合相形成成分としてCoおよびNiのいずれ
か、または両方を含有するダイヤモンド基焼結材
料部材を、同じく結合相形成成分としてCoおよ
びNiのいずれか、または両方を含有する炭化タ
ングステン基超硬合金部材に接合するに際して、
これら両部材の接合面に、少なくともB:3〜20
原子%とC:1〜10原子%を含有し、残りの主要
部がCoおよびNiのいずれか、または両方からな
る配合組成あるいは成分組成を有するろう材を介
在させた状態で、これら両部材を、30Kg/cm2以上
の圧力を付加しながら、750〜900℃の範囲内の所
定温度に加熱して、前記ろう材中のBおよびC成
分を前記両部材内へ拡散させることを特徴とする
ダイヤモンド基焼結材料部材を炭化タングステン
基超硬合金部材に接合する方法。[Claims] 1. A diamond-based sintered material member containing either or both of Co and Ni as a bonding phase forming component, which also contains either or both of Co and Ni as a bonding phase forming component. When joining to tungsten carbide-based cemented carbide members,
At least B: 3 to 20 on the joint surfaces of these two members.
At a pressure of 30 Kg/cm 2 or more, these two members are interposed with a brazing filler metal having a composition or component composition in which Co and/or Ni are included and the remaining main portion is Co and/ or Ni. While adding
A method for joining a diamond-based sintered material member to a tungsten carbide-based cemented carbide member, characterized in that the B component in the brazing filler metal is diffused into both members. 2 A diamond-based sintered material member containing either or both of Co and Ni as a binder phase-forming component, and a tungsten carbide-based cemented carbide member that also contains either or both of Co and Ni as a binder phase-forming component. When joining parts,
At least B: 3 to 20 on the joint surfaces of these two members.
Atomic % and C: 1 to 10 at. , heating to a predetermined temperature within the range of 750 to 900°C while applying a pressure of 30 kg/cm 2 or more to diffuse the B and C components in the brazing filler metal into both members. A method of joining a diamond-based sintered material component to a tungsten carbide-based cemented carbide component.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP3234985A JPS61193770A (en) | 1985-02-20 | 1985-02-20 | Method for joining diamond-base sintered material member to tungsten carbide-base sintered hard alloy member |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP3234985A JPS61193770A (en) | 1985-02-20 | 1985-02-20 | Method for joining diamond-base sintered material member to tungsten carbide-base sintered hard alloy member |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS61193770A JPS61193770A (en) | 1986-08-28 |
| JPH0369860B2 true JPH0369860B2 (en) | 1991-11-05 |
Family
ID=12356481
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP3234985A Granted JPS61193770A (en) | 1985-02-20 | 1985-02-20 | Method for joining diamond-base sintered material member to tungsten carbide-base sintered hard alloy member |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS61193770A (en) |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN109514017B (en) * | 2018-11-28 | 2022-06-28 | 自贡中兴耐磨新材料有限公司 | A Vacuum Diffusion Welding Process of Cemented Carbide and Steel |
-
1985
- 1985-02-20 JP JP3234985A patent/JPS61193770A/en active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| JPS61193770A (en) | 1986-08-28 |
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