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JPH0711049B2 - Cemented carbide and manufacturing method - Google Patents
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JPH0711049B2 - Cemented carbide and manufacturing method - Google Patents

Cemented carbide and manufacturing method

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Publication number
JPH0711049B2
JPH0711049B2 JP1140685A JP14068589A JPH0711049B2 JP H0711049 B2 JPH0711049 B2 JP H0711049B2 JP 1140685 A JP1140685 A JP 1140685A JP 14068589 A JP14068589 A JP 14068589A JP H0711049 B2 JPH0711049 B2 JP H0711049B2
Authority
JP
Japan
Prior art keywords
phase
carbide
solid solution
type solid
grain size
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 - Fee Related
Application number
JP1140685A
Other languages
Japanese (ja)
Other versions
JPH036349A (en
Inventor
仁 堀江
裕介 井寄
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.)
Moldino Tool Engineering Ltd
Original Assignee
Hitachi Tool Engineering 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 Hitachi Tool Engineering Ltd filed Critical Hitachi Tool Engineering Ltd
Priority to JP1140685A priority Critical patent/JPH0711049B2/en
Publication of JPH036349A publication Critical patent/JPH036349A/en
Publication of JPH0711049B2 publication Critical patent/JPH0711049B2/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

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  • Powder Metallurgy (AREA)

Description

【発明の詳細な説明】 [産業上の利用分野] 本発明はP系超硬合金の改良に関する。詳細には、転削
工具の応用範囲の拡大に関する。
DETAILED DESCRIPTION OF THE INVENTION [Industrial field of application] The present invention relates to improvement of P-based cemented carbide. In particular, it relates to expanding the range of applications of rolling tools.

[従来の技術] 硬質相が炭化タングステンとB−1型固溶体からなる超
硬合金はそのすぐれた耐摩耗性と耐衝撃性から様々な用
途に実用化されている。特に、WC-TiC-Ta(Nb)C-Co系にT
iNを微量添加した合金は、その窒素の添加により、前記
の超硬合金よりB−1型固溶体相の微細化が計れ、より
強靱性が要求される用途に使用されている。従来、B−
1型固溶体には、2元系または4元系の固溶体(WTi)
C、(WTiTaNb)C、が使用され、WC-TiC−第3硬質物
質郡(TaC NbC)の擬3元系状態図で示される。FCC相中
へのHCP相の固溶限界に近似した組成で使用されてい
た。このことは、使用されているWCを固溶反応を生じさ
せずに、元の状態のまま、焼結体中に残存させ、粒度分
布の調整をより、しやすくしている効果もある。すなわ
ち、WC相には比較的粗い粒度のものを用いて、B−1型
固溶体の微細化に伴う機械的衝撃、耐塑性変形等の性能
をWCの粗粒化によりバランスをとっている。
[Prior Art] A cemented carbide having a hard phase composed of tungsten carbide and a B-1 type solid solution has been put to practical use in various applications because of its excellent wear resistance and impact resistance. Especially, in WC-TiC-Ta (Nb) C-Co system, T
The alloy to which a small amount of iN is added can be refined in the B-1 type solid solution phase as compared with the above cemented carbide by the addition of nitrogen, and is used for applications requiring higher toughness. Conventionally, B-
Type 1 solid solutions include binary or quaternary solid solutions (WTi)
C, (WTiTaNb) C, was used and is shown in the quasi-ternary phase diagram of WC-TiC-third hard material group (TaC NbC). It was used with a composition close to the solid solubility limit of the HCP phase in the FCC phase. This also has the effect of allowing the used WC to remain in the sintered body in its original state without causing a solid solution reaction, making it easier to adjust the particle size distribution. That is, the WC phase having a relatively coarse grain size is used to balance the performance such as mechanical impact and plastic deformation accompanying the refinement of the B-1 type solid solution by the coarse graining of WC.

[発明が解決しようとする問題点] 上記の様に従来のP系超硬合金は4〜8ミクロンの粗粒
WCと1〜2ミクロンの微粒B−1型固溶体をCoで結合し
たものであり、TiN添加した場合も概略同様であった。
しかし、最近の高速、高能率切削により本系列合金の欠
点として耐摩耗性が不十分切削面粗度が劣る微少
切削に対しチッピングを生じやすい等、問題点も指摘さ
れている。
[Problems to be Solved by the Invention] As described above, the conventional P-based cemented carbide has a coarse grain size of 4 to 8 microns.
WC and a fine B-1 type solid solution having a size of 1 to 2 μm were bonded with Co, and the same was true when TiN was added.
However, due to the recent high-speed, high-efficiency cutting, problems such as chipping are likely to occur as a drawback of this series of alloys in that the wear resistance is insufficient and the cutting surface roughness is inferior to minute cutting.

[問題点を解決する手段] 合金の組成が同じ場合、B−1型固溶体の組成により合
金の耐摩耗性がきまり、B−1型固溶体中のW含有率が
低いほど耐摩耗性は向上する。さらに切削面粗度は合金
の粒度と相関し、比較的粗粒を使用した場合はおとるの
が一般的であり、微少切削におけるチッピングにたいし
ても同様な傾向が確認されている。従って、B−1型固
溶体中のW含有率をさげ、WC、B−1型固溶体とも、あ
る程度まで微細化、均粒化する必要がある。
[Means for Solving Problems] When the composition of the alloy is the same, the wear resistance of the alloy is determined by the composition of the B-1 type solid solution, and the wear resistance improves as the W content in the B-1 type solid solution decreases. . Further, the roughness of the cutting surface correlates with the grain size of the alloy, and is generally taken when relatively coarse grains are used, and a similar tendency has been confirmed for chipping in fine cutting. Therefore, it is necessary to reduce the W content in the B-1 type solid solution so that both WC and the B-1 type solid solution are refined and grain-sized to a certain extent.

B−1型固溶体中のW含有率をさげ耐摩耗性の向上をは
かる方法を種々検討した結果、Tiの添加方法を変えても
焼結中の拡散により平衡状態となり一定となってしま
う。B−1型固溶体に窒化物を添加するとWの固溶を抑
制し、B−1型固溶体の組成を調整することができる。
特に、窒化物としては、TiN、TaNの効果が大きい。また
B−1型固溶体の微細化についても、上記窒化物は効果
が高い。
As a result of various studies on a method of reducing the W content in the B-1 type solid solution to improve wear resistance, even if the method of adding Ti is changed, it will be in an equilibrium state due to diffusion during sintering and will be constant. When a nitride is added to the B-1 type solid solution, the solid solution of W can be suppressed and the composition of the B-1 type solid solution can be adjusted.
Particularly, as a nitride, TiN and TaN have a great effect. Further, the above-mentioned nitride is also effective in miniaturizing the B-1 type solid solution.

WCに関しては出発原料の平均粒度で調整するが、粒度分
布が問題となり、均一化が困難である。そのため、その
粒度調整をB−1型固溶体中へのWC固溶化に伴う細かな
WC粒子の消滅により均粒化を行うことを見いだしたので
ある。
Although WC is adjusted by the average particle size of the starting material, the particle size distribution becomes a problem and it is difficult to make it uniform. Therefore, it is necessary to adjust the particle size finely with the solidification of WC in the B-1 type solid solution.
They found that the WC particles disappeared to make the particles uniform.

[作用] 以上のごとく、本発明は炭化チタン6〜11%、窒化チタ
ン1〜10%、炭化タンタル及び/または窒化タンタル及
び/または炭化ニオブ6〜12%、残り、炭化タングステ
ンからなる硬質相80〜95%、鉄族金属からなる結合相5
〜20%(以下重量パーセント)からなる超硬合金におい
て焼結体に於ける平均粒度が炭化タングステン相(α
相)1.5ミクロン以下、B−1型固溶体(β相)2ミク
ロン以下よりなり、またその粒度調整をB−1型固溶体
中へのWC固溶化により粒子の微細化、均粒化を行うこと
を特徴とする超硬合金の製造方法である。
[Operation] As described above, according to the present invention, the hard phase 80 is composed of titanium carbide 6 to 11%, titanium nitride 1 to 10%, tantalum carbide and / or tantalum nitride and / or niobium carbide 6 to 12%, and the balance is tungsten carbide. ~ 95%, binder phase consisting of iron group metal 5
The average grain size in the sintered body of the cemented carbide consisting of ~ 20% (hereinafter referred to as weight percent) is the tungsten carbide phase (α
Phase) 1.5 micron or less, B-1 type solid solution (β phase) 2 micron or less, and the particle size adjustment is to make the particles fine and uniform by WC solid solution in the B-1 type solid solution. It is a characteristic method for producing a cemented carbide.

本発明による超硬合金の組成は以下の理由により限定さ
れる。
The composition of the cemented carbide according to the present invention is limited for the following reasons.

1) TiC添加量は、6%未満では耐クレーター性への
効果が少なく、12%を越えると著しく靱性を阻害するた
めに、6〜12%とした。
1) If the TiC content is less than 6%, the effect on crater resistance is small, and if it exceeds 12%, the toughness is significantly impaired.

2) TiN添加量はB−1型固溶体中のTi/Wの比率を決
定する必須な添加物であり、1%未満では、その効果が
少なく、10%を越えると著しく靱性を阻害するために、
1〜10%とした。
2) The amount of TiN added is an essential additive that determines the Ti / W ratio in the B-1 type solid solution. If it is less than 1%, its effect is small, and if it exceeds 10%, the toughness is significantly impaired. ,
It was set to 1 to 10%.

3) TaC、TaN、NbCの添加量は、6%未満では、粒抑
制への効果が少なく、12%を越えて添加しても顕著な効
果がないため6〜12%とした。
3) The addition amount of TaC, TaN, and NbC is less than 6%, the effect of suppressing grain is small, and the addition amount of more than 12% has no significant effect.

4) 鉄族金属の添加量は、5%未満では十分な靱性が
得られず、20%をこえると耐塑性変形性、耐摩耗性を悪
くするため、5〜20%とした。
4) The addition amount of the iron group metal is less than 5%, sufficient toughness cannot be obtained, and if it exceeds 20%, plastic deformation resistance and wear resistance are deteriorated.

5) WC相の粒度は、焼結体での粒度が1.5ミクロンを
こえると、切削面粗度が悪くなるため、1.5ミクロン以
下とした。
5) The grain size of the WC phase was set to 1.5 microns or less because the cutting surface roughness deteriorates when the grain size of the sintered body exceeds 1.5 microns.

6)B−1型固溶体相の粒度は、焼結体での粒度が2ミ
クロンをこえると、WC相に比較し脆い相なため、強度が
劣化しチッピングしやすくなるため、2ミクロン以下と
したが、望ましくは1.5ミクロン以下が良い。
6) The grain size of the B-1 type solid solution phase is set to 2 μm or less because if the grain size in the sintered body exceeds 2 μm, it is a more brittle phase than the WC phase and the strength deteriorates and chipping easily occurs. However, 1.5 micron or less is desirable.

7) B−1型固溶体中へのWC固溶化は、WC-TiC-TaC系
では、TaCの量に依らずほぼWC/TiC=70/30の比率とな
る。しかし、この系の一部にTiNを添加すると、この比
率は図2.に示すように、Wの含有率が変化し、Tiに富む
組成となる。この組成は出発原料によらず、ほぼ一定と
なる。例えばWC/TiC固溶体を用いた場合には、平衡状態
より過飽和となるため、焼結中にWCが析出し、WC、TiC
を単独または飽和しない状態で用いた場合では、WCを吸
収する。この状態は、WCが粗粒の場合には、焼結時の安
定性を計るため、トリプルカーバイドまたはダブルカー
バイドと称する予め固溶体を作成し調整したほうがWC粒
度の管理も行い易い等の効果もあった。しかし、WCの微
粒化を計る場合には、混合等に依って生ずるWCの微粉を
焼結中にB−1型固溶体中に取り込み、均粒化をはかる
のに効果を発揮する。以下本発明を実施例に基づき詳細
に説明する。
7) In the WC-TiC-TaC system, the WC solid solution in the B-1 type solid solution is almost WC / TiC = 70/30 regardless of the amount of TaC. However, when TiN is added to a part of this system, this ratio changes the W content, as shown in Fig. 2, resulting in a Ti-rich composition. This composition is almost constant regardless of the starting material. For example, when a WC / TiC solid solution is used, it becomes oversaturated from the equilibrium state, so WC precipitates during sintering, and WC, TiC
Absorbs WC when used alone or in an unsaturated state. In this state, when WC is coarse-grained, in order to measure the stability during sintering, it is easier to control the WC particle size by preparing and adjusting a solid solution called triple carbide or double carbide beforehand. It was However, when pulverizing WC, fine powder of WC produced by mixing or the like is taken into the B-1 type solid solution during sintering, and it is effective for achieving uniform grain size. Hereinafter, the present invention will be described in detail based on examples.

[実施例] 71WC-10TiC-10TaC-9Coの組成になるよう配合した。配合
に使用した原料は市販のWC粉末(平均粒度1.0μm及び
5.0μm)、TiC粉末(同1.0μm)、TiN粉末(同1.0μ
m)、DC粉末(WC/TiC=70/30 同1.5μm)、DC粉末
(WC/TiC=50/50 同1.0μm)、及び、上記粉末を使用
してWC-TiC-TiNの固溶体を作成した。固溶体はWC/TiC
/TiN=6/3/1 WC/TiC/TiN=4/4/2 となるよう配合
し、乾燥後、1600℃2時間、N雰囲気中で固溶化処理
し、粒度調整を行い、平均粒度0.8μmの粉末を作成し
た。
[Example] 71WC-10TiC-10TaC-9Co was compounded to have a composition. The raw materials used for blending were commercially available WC powders (average particle size 1.0 μm and
5.0 μm), TiC powder (1.0 μm), TiN powder (1.0 μm)
m), DC powder (WC / TiC = 70/30 1.5 μm), DC powder (WC / TiC = 50/50 1.0 μm), and a solid solution of WC-TiC-TiN using the above powder. did. WC / TiC solid solution
/ TiN = 6/3/1 WC / TiC / TiN = 4/4/2 were blended, dried, and subjected to solution treatment at 1600 ° C for 2 hours in N atmosphere to adjust the particle size, and the average particle size 0.8 A μm powder was prepared.

これらの粉末を第1表に示す様に種々な方法で混合し
た。その混合終了後、乾燥した後、TEE433のスローアウ
ェイチップをプレス成形し、真空中1400℃ 1hr 焼結
したのち、所定の形状に加工した。
These powders were mixed in various ways as shown in Table 1. After the completion of the mixing, after drying, a throw away tip of TEE433 was press-molded, sintered at 1400 ° C. for 1 hr in vacuum, and then processed into a predetermined shape.

また、物性、ミクロ組織上の変化を確認するため、上記
チップを研磨、ラップした後、硬さ、破壊靱性値を測定
した。その結果も併せて併記する。また、粒度は電子顕
微鏡による組織観察を行い、その写真より測定した。本
発明1と比較例10の測定結果は、本発明1がWC相の平均
粒度は1.05μm、B−1型固溶体は0.91μmであり、比
較例10は、WC相の平均粒度は4.0μm、B−1型固溶体
は2.5μmと粗く成っていた。さらに、切削性能を確認
するため、下記の諸元でおこなった。
Further, in order to confirm changes in physical properties and microstructure, the chips were polished and wrapped, and then hardness and fracture toughness values were measured. The results are also shown together. The grain size was measured by observing the structure with an electron microscope and observing the photograph. The measurement results of Inventive Example 1 and Comparative Example 10 are that the invention 1 has an average particle size of the WC phase of 1.05 μm and the B-1 type solid solution is 0.91 μm, and Comparative Example 10 has an average particle size of the WC phase of 4.0 μm. The B-1 type solid solution was coarse, 2.5 μm. Furthermore, in order to confirm cutting performance, the following specifications were performed.

切削速度 150m/min 送り 0.08mm/刃 切込み 1.0mm 被削材 SUS304 チップ形状 TEE433 カッター形状 φ63 3枚刃 寿命基準 VB=0.2mmまでの切削時間(min) その結果も表1.に併せて併記する。Cutting speed 150m / min Feed 0.08mm / blade Depth of cut 1.0mm Work material SUS304 Tip shape TEE433 Cutter shape φ63 3 blades Life standard VB = 0.2mm Cutting time (min) The results are also shown in Table 1. .

第1表の結果より、硬さと破壊靱性値の関係がWC粒度の
違いにより、ある程度の差があるが、これらの切削試験
においては、粒度の影響が現れ、比較例は使用初期〜中
期にチッピングにより寿命に達したのに対し、本発明例
は正常摩耗により長寿命化が達成されている。また切削
面の粗さも良好である。
From the results shown in Table 1, the relationship between hardness and fracture toughness value varies to some extent depending on the difference in WC grain size, but in these cutting tests, the effect of grain size appears, and the comparative examples show chipping during the early to middle stages of use. However, in the example of the present invention, a longer life is achieved by normal wear. The roughness of the cutting surface is also good.

[発明の効果] P系超硬合金において、焼結体に於ける窒化物添加、及
び製法を調整することにより焼結体における平均粒度を
炭化タングステン相(α相)1.5ミクロン以下、B−1
型固溶体相(β相)1ミクロン以下と微細化を計ること
により微小切削等において、耐チッピング性、耐摩耗性
に優れた超硬合金を開発した。
[Effects of the Invention] In P-based cemented carbide, the average grain size in the sintered body is adjusted to be 1.5 μm or less in the tungsten carbide phase (α phase) by adjusting the addition of a nitride in the sintered body and the manufacturing method.
We have developed a cemented carbide with excellent chipping resistance and wear resistance in micro-cutting, etc. by making the mold solid solution phase (β phase) finer than 1 micron.

【図面の簡単な説明】[Brief description of drawings]

第1図は、WC-TiC-TaCの擬3元系状態図、第2図は、WC
-TiCN-TaCの擬3元系状態図を示す。
Figure 1 shows the quasi-ternary phase diagram of WC-TiC-TaC, and Figure 2 shows WC.
-TiCN-TaC quasi-ternary phase diagram is shown.

Claims (2)

【特許請求の範囲】[Claims] 【請求項1】炭化チタン6〜11%、窒化チタン1〜10
%、炭化タンタル及び/または窒化タンタル及び/また
は炭化ニオブ6〜12%残り、炭化タングステンからなる
硬質相80〜95%、鉄族金属からなる結合相5〜20%(以
下重量パーセント)からなる超硬合金において、焼結体
に於ける平均粒度が炭化タングステン相(α相)1.5ミ
クロン以下、B−1型固溶体(β相)2ミクロン以下よ
りなることを特徴とする超硬合金。
1. Titanium carbide 6 to 11%, titanium nitride 1 to 10
%, Tantalum carbide and / or tantalum nitride and / or niobium carbide 6-12% remaining, hard phase 80-95% made of tungsten carbide, binder phase 5-20% (hereinafter weight percent) made of iron group metal A cemented carbide, characterized in that, in a hard alloy, the average grain size in a sintered body is a tungsten carbide phase (α phase) of 1.5 microns or less and a B-1 type solid solution (β phase) of 2 microns or less.
【請求項2】炭化チタン6〜11%、窒化チタン1〜10
%、炭化タンタル及び/または窒化タンタル及び/また
は炭化ニオブ6〜12%残り、炭化タングステンからなる
硬質相80〜95%、鉄族金属からなる結合相5〜20%(以
上重量パーセント)からなる超硬合金において、その粒
度調整をB−1型固溶体中へのWC固溶化により行うこと
を特徴とする超硬合金の製造方法。
2. Titanium carbide 6 to 11%, titanium nitride 1 to 10
%, Tantalum carbide and / or tantalum nitride and / or niobium carbide 6 to 12% remaining, tungsten carbide hard phase 80 to 95%, iron group metal binder phase 5 to 20% (above weight percent) A method for producing a cemented carbide, characterized in that the grain size of the hard alloy is adjusted by WC solid solution in a B-1 type solid solution.
JP1140685A 1989-06-02 1989-06-02 Cemented carbide and manufacturing method Expired - Fee Related JPH0711049B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP1140685A JPH0711049B2 (en) 1989-06-02 1989-06-02 Cemented carbide and manufacturing method

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP1140685A JPH0711049B2 (en) 1989-06-02 1989-06-02 Cemented carbide and manufacturing method

Publications (2)

Publication Number Publication Date
JPH036349A JPH036349A (en) 1991-01-11
JPH0711049B2 true JPH0711049B2 (en) 1995-02-08

Family

ID=15274375

Family Applications (1)

Application Number Title Priority Date Filing Date
JP1140685A Expired - Fee Related JPH0711049B2 (en) 1989-06-02 1989-06-02 Cemented carbide and manufacturing method

Country Status (1)

Country Link
JP (1) JPH0711049B2 (en)

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5919176B2 (en) * 1978-12-29 1984-05-02 住友電気工業株式会社 cemented carbide
JPS602647A (en) * 1983-06-20 1985-01-08 Mitsubishi Metal Corp Tungsten carbide-base sintered hard alloy for cutting tool
JPH0657865B2 (en) * 1987-01-13 1994-08-03 日立ツ−ル株式会社 Superfine cemented carbide

Also Published As

Publication number Publication date
JPH036349A (en) 1991-01-11

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