JPS6043457A - Sintered hard alloy for cutting - Google Patents

Sintered hard alloy for cutting

Info

Publication number
JPS6043457A
JPS6043457A JP15113083A JP15113083A JPS6043457A JP S6043457 A JPS6043457 A JP S6043457A JP 15113083 A JP15113083 A JP 15113083A JP 15113083 A JP15113083 A JP 15113083A JP S6043457 A JPS6043457 A JP S6043457A
Authority
JP
Japan
Prior art keywords
carbide
cutting
molybdenum
hard alloy
sintered hard
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.)
Pending
Application number
JP15113083A
Other languages
Japanese (ja)
Inventor
Yusuke Iyori
裕介 井寄
Norio Takahashi
紀雄 高橋
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.)
Proterial Ltd
Original Assignee
Hitachi Metals 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 Metals Ltd filed Critical Hitachi Metals Ltd
Priority to JP15113083A priority Critical patent/JPS6043457A/en
Publication of JPS6043457A publication Critical patent/JPS6043457A/en
Pending legal-status Critical Current

Links

Abstract

PURPOSE:To obtain a sintered hard alloy fit for dry and wet cutting conditions during cutting ranging from low speed to high speed by adding Nb carbide, Hf carbide, HfN, TaN, NbN, ZrN, Mo, Mo2C and an iron group metal to WC and TiC so as to provide a specified composition and a specified ratio of Nb carbide/Hf carbide. CONSTITUTION:This sintered hard alloy consists of, by weight, 10-60% WC, 5-40% TiC, 5-30% in total of Nb carbide and Hf carbide, 3-<20% in total of one or more among HfN, TaN, NbN and ZrN, 0.5-<5% Mo or Mo2C, and 5-20% iron group metal such as Co, Ni or Fe. In the alloy, the weight ratio of Nb carbide/Hf carbide is 1/10-10/3.

Description

【発明の詳細な説明】 本発明はフライス加工や旋削加工等に使用する切削用超
硬合金に関するものである。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a cutting cemented carbide used for milling, turning, etc.

従来、フライス切削等に使用されている超硬合金には炭
化タングステン基および炭化チタン基超硬合金がある。
Conventionally, cemented carbide used for milling and the like include tungsten carbide-based and titanium carbide-based cemented carbide.

前者の炭化タングステン基超硬合金においては、炭化チ
タン基超硬合金に比較してクレータ摩耗が大きい欠点が
ある。
The former tungsten carbide-based cemented carbide has the disadvantage of greater crater wear compared to titanium carbide-based cemented carbide.

他方、炭化チタン基超硬合金は炭化タングステン基超硬
合金よりも硬度が高く、耐熱性が優れているので、高速
切削用に広く用いられているが、炭化タングステン基超
硬合金よりも靭性に乏しく、機械的画状、熱衝撃に弱い
欠点がある。またこの炭化チタン基超硬合金は熱伝導性
が炭化タングステン基超硬合金より悪く、切削中に刃先
の部分が局部的に熱せられることによって、刃先にクラ
ックを生じ急冷させると破損することがある。
On the other hand, titanium carbide-based cemented carbide has higher hardness and better heat resistance than tungsten carbide-based cemented carbide, so it is widely used for high-speed cutting, but it has lower toughness than tungsten carbide-based cemented carbide. It has the drawbacks of poor mechanical patterning and poor thermal shock resistance. In addition, this titanium carbide-based cemented carbide has poorer thermal conductivity than tungsten carbide-based cemented carbide, and when the cutting edge is locally heated during cutting, the cutting edge may crack and break if rapidly cooled. .

このように炭化タングステン墨超硬合金および炭化チタ
ン基超硬合金はそれぞれの欠点により切削条件の適合範
囲がかなり制限されている。
As described above, the range of suitable cutting conditions for tungsten carbide black cemented carbide and titanium carbide based cemented carbide is considerably limited due to their respective drawbacks.

本発明は、上記従来のような炭化タングステン基および
炭化チタン基超硬合金の欠点を改良し、フライス切削等
において低速切削から高速切削まで適用でさ、また乾式
切削および湿式切削のいずれの切削条件にも適合でさ、
従来の切削用超硬合金よりもより使い易い切削用超硬合
金を得ることを目的とするものである。
The present invention improves the drawbacks of the conventional tungsten carbide-based and titanium carbide-based cemented carbide, and can be applied to milling, etc., from low-speed cutting to high-speed cutting, and can be applied under both dry cutting and wet cutting conditions. It is also suitable for
The object is to obtain a cemented carbide for cutting that is easier to use than conventional cemented carbide for cutting.

本発明は、重石比で、炭化タングスデン10〜60%、
炭炭化チタン5〜4亢 ニウムの合81m5〜30%,ハフニウム、タンタル。
The present invention has a weight ratio of tungden carbide of 10 to 60%,
81 m 5-30% titanium carbide, hafnium, tantalum.

二Aブ,ジルコニウムの窒化物のうちの1種又は2種以
」−の合計量が3%以上20%未満,モリブデンまたは
炭化モリブデン0.5%以上5%未満,コバルト、ニッ
ケル、鉄等の鉄族金fFja5〜20%の成分からなる
ことを特徴とする。
3% or more and less than 20% of one or more nitrides of aluminum, zirconium, molybdenum or molybdenum carbide, 0.5% or more and less than 5% of molybdenum or molybdenum carbide, cobalt, nickel, iron, etc. It is characterized by consisting of 5 to 20% iron group gold fFja.

この組成によって、従来の炭化チタン基超硬含金j;り
も耐熱性に優れ、抗折力の大幅な低下を起さずに硬度が
高められ、かつ広範囲な切削条件【こ適合づることがで
きる。
This composition has superior heat resistance compared to conventional titanium carbide-based cemented carbide alloys, increases hardness without significantly reducing transverse rupture strength, and can be adapted to a wide range of cutting conditions. can.

ところで、鋼或いは高級鋳鉄の切削では二番摩耗および
づ−くい面摩耗を軒減する要素として炭化チタンに及ぶ
ものはない。従ってできる限り炭化チタンの比率を大き
くする方が摩耗に関Jる限り右利であるが、他方炭化チ
タンの熱伝導率が非常に低いことに起因する種々の問題
が生ずる場合がある。炭化チタンを効率よく使用するた
めに炭化タングスデン,炭化タンタル、炭化ニオブ、炭
化ハフニウム等を固溶させて使用することが考えられる
が、この場合焼結時に固溶体同志が接触した部分から互
いに融合して大さな粒子に成長しゃすい。この粒子の大
きさは工具摩耗の大きな影響因子である。
By the way, when cutting steel or high-grade cast iron, there is nothing that can match titanium carbide as an element for reducing secondary wear and cutting face wear. Therefore, it is advantageous to increase the proportion of titanium carbide as much as possible as far as wear is concerned, but on the other hand, various problems may occur due to the extremely low thermal conductivity of titanium carbide. In order to use titanium carbide efficiently, it is possible to use tungsten carbide, tantalum carbide, niobium carbide, hafnium carbide, etc. as a solid solution. It grows into large particles. The size of these particles is a major influence factor on tool wear.

、 しかして窒化物を適m添加すると、この粒成長を妨
げることができる。即ら、窒化物は炭化チタン基超硬合
金に特有な炭化チタンを核に持つ有核組織を保ったまま
、その炭化チタンに多く見られる固溶体粒子の粒成長を
抑制し、結晶粒を微細にすることかで・きる。また窒化
物は概して炭化チタンに比べ熱衝撃抵抗も大きく、鋼と
の間の摩擦係数が小さいIこめ発熱M目体も小さくなり
、従来の炭化チタン基超硬合金よりも、耐熱衝撃性か改
善される。このように窒化チタンの添加にJこって粒の
微細化が行なわれるために硬度が高く、耐摩耗性が著し
く向上し、一般の乾式フライス切削等だけでなく、湿式
のフライス切削等においても、カケやヂップングを起づ
ことが少なく、また比較的低チタンで高い切削性0ヒを
示ず超硬合金が得られる。
However, by adding an appropriate amount of nitride, this grain growth can be inhibited. In other words, nitride suppresses the grain growth of solid solution particles often found in titanium carbide, making the crystal grains finer, while maintaining the nucleated structure with titanium carbide as the core, which is unique to titanium carbide-based cemented carbide. I can do it by doing something. In addition, nitrides generally have higher thermal shock resistance than titanium carbide, have a smaller coefficient of friction with steel, and have smaller heat generating bodies, resulting in improved thermal shock resistance than conventional titanium carbide-based cemented carbides. be done. In this way, the addition of titanium nitride makes the grains finer, resulting in higher hardness and significantly improved wear resistance, making it suitable for not only general dry milling but also wet milling. A cemented carbide can be obtained that rarely causes chipping or dipping, and has a relatively low titanium content and exhibits high machinability.

炭化チタンおよび硬質窒化物の含有ωはそれぞれ前述の
範囲が好ましく、それを越えると靭性が乏しくなり、ま
た上記範囲以下では充分な耐熱性耐摩耗性がi%られな
い。
The content ω of titanium carbide and hard nitride is preferably within the above-mentioned ranges; if it exceeds this range, the toughness will be poor, and if it is below the above-mentioned range, sufficient heat resistance and wear resistance will not be achieved i%.

ここで硬質窒化物としては、Hf N,Ta N。Here, the hard nitrides include HfN and TaN.

NbN,ZrNから選ばれることが特に必須条件である
。その理由は次に由る。
It is particularly essential that the material be selected from NbN and ZrN. The reason is as follows.

づなわら、本発明合金の主要B,)酸成分はTiCおよ
びWCであるが、WC中には一般には窒化物が161溶
せず、窒化物は主としてTiCと固溶体をつくることに
なる。この場合、Ti金属とは異なる1−1F 、 1
−a 、 Nb 、 Zr等の窒化物ト(7) 固rf
J 体を形成さけると、TiCとTiNの固溶体よりも
硬さが急激に向上し、切削性能上りrましい結果となる
The main acid components of the alloy of the present invention are TiC and WC, but nitrides generally do not dissolve in WC, and nitrides mainly form a solid solution with TiC. In this case, 1-1F, 1 which is different from Ti metal
-Nitrides such as a, Nb, Zr etc. (7) Hard rf
If the formation of a J-body is avoided, the hardness will be sharply improved compared to a solid solution of TiC and TiN, resulting in poor cutting performance.

炭化ハフニウムおよび炭化ニオブは前述のように炭化チ
タンを効率よく含有さゼるために用いられるものである
が、特にN11Cと1−1fcを共存して使用づること
により、合金の耐摩耗性,高温での耐変形性が著しく向
上することを発明者等は兄出しIC0 ここで、NbC/l−1fc重量比は1/10〜10/
′3の範囲が望ましく、この範囲外では、耐摩耗性。
As mentioned above, hafnium carbide and niobium carbide are used to efficiently contain titanium carbide, but by using N11C and 1-1fc together, the wear resistance and high temperature properties of the alloy can be improved. The inventors have found that the deformation resistance is significantly improved at IC0, where the NbC/l-1fc weight ratio is 1/10 to 10/
A range of '3 is desirable; outside this range, the wear resistance is poor.

耐変形性の著しい向上は望めない。No significant improvement in deformation resistance can be expected.

特に本発明において、注目すべき貞はモリブデンまたは
炭化モリブデンの添加量である。
Particularly in the present invention, what is noteworthy is the amount of molybdenum or molybdenum carbide added.

すなわら、モリブデンまたは炭化モリブデンは焼結性及
び高温での耐変形性の二点に著しい効果があることを発
明者らは見出した。
In other words, the inventors have discovered that molybdenum or molybdenum carbide has remarkable effects on two points: sinterability and deformation resistance at high temperatures.

TiC−Ni合金において、MOをNi量に対し約半分
程度添加すると焼結性が著しく向上することは既に周知
であるが、ざらにWCが加わった系においては、ごく微
量のMOを添加するだけでも焼結性改善効果が顕著であ
ることを種々検討を加えた結果、発明者らは見出した。
It is already well known that the sinterability of TiC-Ni alloys is significantly improved by adding about half the amount of MO to the amount of Ni, but in systems where WC is added, only a very small amount of MO is added. However, as a result of various studies, the inventors discovered that the effect of improving sinterability is significant.

さらに水系合金は硬質窒化物が加わっているために硬質
粒子が非常にm細となり、ぞの結果常温における靭性は
優れるものの、MOを添加しない場合には高)局におけ
る耐変形性く耐クリープ性)に劣ることが確められる。
Furthermore, since hard nitrides are added to water-based alloys, the hard particles become very thin.As a result, although they have excellent toughness at room temperature, they have high deformation resistance and creep resistance when MO is not added. ) is confirmed to be inferior to

MOはこの高温における耐変形性を激的に改善し、ひい
ては切削時の耐摩耗性を向上さけることを発明者らは見
出した。
The inventors have discovered that MO dramatically improves the deformation resistance at high temperatures and, in turn, improves the wear resistance during cutting.

ここで、モリブデンまたは炭化モリブデンの最適量は0
.5%以上5%未満で、0.5%未満では焼結性改善に
効果が少なく、5%を越えるとこすりに対する耐摩耗性
が減する。モリブデンまたは炭化モリブデンの最適添加
量をこの範囲に選ぶことが大きなポイントで、この点で
特公昭58−9137号と峻別せられるべきものである
Here, the optimal amount of molybdenum or molybdenum carbide is 0
.. If it is 5% or more and less than 5%, if it is less than 0.5%, it will have little effect on improving sinterability, and if it exceeds 5%, the wear resistance against rubbing will decrease. The important point is to select the optimum amount of molybdenum or molybdenum carbide to be added within this range, and in this respect it should be clearly distinguished from Japanese Patent Publication No. 58-9137.

以上)ホべた組成を選ぶことにより、連続切削断続切削
共に1Ωれた効果が得られる。
(above) By selecting the desired composition, it is possible to obtain the effect of lowering the resistance by 1Ω in both continuous cutting and interrupted cutting.

実施例 WC−10%TiC−5%Zr N −3,5%NbC
−3,5%ト」fC−3%MO2C−12%Niなる組
成に配合し、ボールミルにて72時間混合した後加圧成
形し、1400℃で焼結した。(試料A)また、比較材
としてMO2Cを添加しない試料Bも同時に作製し、両
者を比較した。試料Aの抗折力値は240kg 71m
2.試料Bのそれは180?l /mm2であり、MO
2Cを添加することにより焼結性が大幅に向上した。
Example WC-10%TiC-5%ZrN-3,5%NbC
-3.5% fC - 3% MO2C - 12% Ni, mixed in a ball mill for 72 hours, then pressure molded and sintered at 1400°C. (Sample A) In addition, as a comparison material, Sample B to which no MO2C was added was also produced at the same time, and the two were compared. The transverse rupture strength value of sample A is 240 kg 71 m
2. Is it 180 for sample B? l/mm2, and MO
Sinterability was significantly improved by adding 2C.

また、1000℃における72kg/mm2の応力下に
おける歪速度を測定したところ、A試料は0.0012
−4゜ ×107分、B試料は4,5x +o、l’分となり、
MO2C添加により耐変形性が著しく向上することが確
められた。
In addition, when the strain rate under a stress of 72 kg/mm2 at 1000°C was measured, the strain rate of sample A was 0.0012
-4° x 107 minutes, sample B becomes 4,5x +o, l' minutes,
It was confirmed that the addition of MO2C significantly improved deformation resistance.

次に旋盤を用いて切削7ス[・を実施した。Next, 7 steps of cutting were performed using a lathe.

切削緒元は、切削速度180m/分、切込み2mm 。The cutting specifications are a cutting speed of 180 m/min and a depth of cut of 2 mm.

送り0.3mm7’回転、被削U S CM 440で
あった。
The feed was 0.3 mm, 7' rotation, and the workpiece was US CM 440.

25分切削後、試料へのフランク摩耗幅はO、OG n
l Ill試料Bのフランク摩耗幅は0.33mn1で
あった。
After 25 minutes of cutting, the flank wear width on the specimen is O, OG n
The flank wear width of Sample B was 0.33 mn1.

以上説明したように、本発明によれば、常温に83ける
抗折強度の向上と共に高温にお(〕る耐変形性を改善で
さ、耐摩耗性、耐熱衝撃性に富む切削用超硬合金を得る
ことが−Cさる。
As explained above, according to the present invention, a cemented carbide for cutting has improved bending strength at room temperature and improved deformation resistance at high temperatures. It is possible to obtain −C.

Claims (1)

【特許請求の範囲】[Claims] 重量比で炭化タングスデン10〜60%、炭化チタン5
・〜40%、炭化ニオブと炭化ハフニウムの合計f55
〜30%、Hf N、Ta N、Nb N、Zr Nの
°うらの1種又は2種以上を合計量で、3%以上20%
未満、モリブデンまたは炭化モリブデン0.5%以上5
%未満、コバルト、ニッケル、鉄などの鉄71χ金属5
・〜20%の成分からなり、かつ炭化ニオブ/′炭化ハ
フニウム重量比が1/’10〜10/3の範囲にあるこ
とを特徴どする切削用超硬合金。
Tungsden carbide 10-60%, titanium carbide 5% by weight
・~40%, total of niobium carbide and hafnium carbide f55
~30%, total amount of one or more of HfN, TaN, NbN, ZrN, 3% or more 20%
Less than 0.5% of molybdenum or molybdenum carbide 5
Less than %, iron 71χ metals such as cobalt, nickel, iron, etc.5
- A cemented carbide for cutting, comprising ~20% of the component and having a weight ratio of niobium carbide/'hafnium carbide in the range of 1/'10 to 10/3.
JP15113083A 1983-08-19 1983-08-19 Sintered hard alloy for cutting Pending JPS6043457A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP15113083A JPS6043457A (en) 1983-08-19 1983-08-19 Sintered hard alloy for cutting

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP15113083A JPS6043457A (en) 1983-08-19 1983-08-19 Sintered hard alloy for cutting

Publications (1)

Publication Number Publication Date
JPS6043457A true JPS6043457A (en) 1985-03-08

Family

ID=15512018

Family Applications (1)

Application Number Title Priority Date Filing Date
JP15113083A Pending JPS6043457A (en) 1983-08-19 1983-08-19 Sintered hard alloy for cutting

Country Status (1)

Country Link
JP (1) JPS6043457A (en)

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