JPS634896B2 - - Google Patents
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- Publication number
- JPS634896B2 JPS634896B2 JP5212085A JP5212085A JPS634896B2 JP S634896 B2 JPS634896 B2 JP S634896B2 JP 5212085 A JP5212085 A JP 5212085A JP 5212085 A JP5212085 A JP 5212085A JP S634896 B2 JPS634896 B2 JP S634896B2
- Authority
- JP
- Japan
- Prior art keywords
- cermet
- dispersed phase
- hard dispersed
- less
- cermets
- 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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- Cutting Tools, Boring Holders, And Turrets (AREA)
Description
〔産業上の利用分野〕
この発明は、高硬度と高靭性を有し、特に切削
工具として用いた場合に、すぐれた耐摩耗性と耐
欠損性を示し、長期に亘つてすぐれた切削性能を
発揮するサーメツトに関するものである。
〔従来の技術とその問題点〕
従来、切削工具用サーメツトとして、硬質分散
相の主要部が炭化チタン(以下TiCで示す)で構
成され、一方結合相の主要部がNiおよびCoのう
ちのいずれか、または両方で構成されたTiC基サ
ーメツトが知られているが、このTiC基サーメツ
トは高硬度をもつものの、靭性の劣るものである
ため、靭性が要求される切削条件下での使用では
欠損を起して実用に耐えないものである。
また、近年、高硬度および高靭性を有する切削
工具用サーメツトとして、硬質分散相の主要部が
炭窒化チタン(以下TiCNで示す)で構成され、
一方結合相の主要部が、同様にNiおよびCoのい
ずれか、または両方で構成されたTiCN基サーメ
ツトも提案されているが、このTiCN基サーメツ
トは焼結性の劣るものであるため、性質のバラツ
キが大きく、信頼性の劣るものである。
〔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、高硬度と高靭性を有し、かつ性質のバラツキ
がなく、しかも切削工具として用いた場合にすぐ
れた切削性能を発揮するサーメツトを開発すべく
研究を行なつた結果、
原料粉末として、TiC粉末、炭化タンタル(以
下TaCで示す)粉末、炭化ニオブ(以下NbCで
示す)粉末、並びにこれらの2種以上の固溶体粉
末、さらに窒化チタン(以下TiNで示す)粉末、
窒化タンタル(以下TaNで示す)粉末、窒化ニ
オブ(以下NbNで示す)粉末、Ni粉末、および
Co粉末を用意し、これら原料粉末を所定の配合
組成に配合し、通常の条件で混合し、圧粉体をプ
レス成形した後、この圧粉体を、液相が出現する
まで真空雰囲気とし、液相出現後は0.1〜10torr
の範囲内の圧力を有する窒素雰囲気とする条件で
焼結すると、
硬質分散相が、70〜90重量%の有芯構造を有す
る、
(a) Tiと、Taの複合炭窒化物、
(b) Tiと、TaおよびNb(ただしNbはTaの50原
子%以下)の複合炭窒化物、
以上(a)および(b)のいずれかからなり、
一方、残りの10〜30重量%の結合相が、重量%
で、
Ti:0.5〜5%、
Ta、またはTaとNb(ただしNbはTaの50%以
下):0.1〜3%、
を固溶含有し、残りがNiおよびCoのうちのいず
れか、または両方と不可避不純物からなる組成を
有する合金で構成され、かつ、
上記硬質分散相を、組成式:
{Ti〓(Ta、Nb)〓}(CxNy)z
で現わした場合、原子比で、
α+β=1、x+y=1、
0.6≦α≦0.9、0.50≦x≦0.90、
0.1≦β≦0.4、0.10≦y≦0.50、
0.85≦z≦1.00、
を満足すると共に、
上記硬質分散相の有芯構造を構成する芯部が、
原子%で、
Ti:45〜49.5%、
Ta、またはTaとNb(ただしNbはTaの50%以
下):0.5〜5%、
C:25〜45%、
N:5〜25%、
からなる組成を有し、一方同周辺部は、同じく原
子%で、
Ti:25〜45%、
Ta、またはTaとNb(ただしNbはTaの50%以
下):5〜25%、
C:35〜47.5%、
N:2.5〜15%、
からなる組成を有し、さらに、
Cの含有量は周辺部の方が芯部よりも高く、N
の含有量は芯部の方が周辺部よりも高い濃度分布
をもつたサーメツトが得られ、この結果のサーメ
ツトは、高硬度および高靭性を有し、かつ良好な
焼結性をもつので性質上のバラツキがなく、した
がつて、これを切削工具として用いた場合には、
すぐれた耐摩耗性と耐欠損性を安定して発揮する
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、以下にサーメツトにおける限定理由
を説明する。
(a) 硬質分散相および結合相の含有量
硬質分散相には、サーメツトの硬さを向上さ
せて、耐摩耗性を著しく改善する作用がある
が、その割合がサーメツトに占める割合で70重
量%未満では、相対的に結合相の割合が30重量
%を越えて多くなり過ぎ、サーメツトの耐摩耗
性が著しく低下するようになり、一方その割合
が同じくサーメツトに占める割合で90重量%を
越えると、相対的に結合相の割合が10重量%未
満となつて、サーメツトの耐欠損性が著しく低
下するようになることから、その割合をサーメ
ツト全体に占める割合で70〜90重量%と定め
た。
(b) 硬質分散相の組成式におけるαの値
Tiは硬質分散相の主体成分であると共に、
主にこれの芯部を形成してサーメツトの硬さを
向上させ、もつて耐摩耗性を向上させる作用を
もつが、その割合が硬質分散相の金属成分に占
める割合(原子比)で0.6未満では、所望の耐
摩耗性を確保することができず、一方その割合
が同0.9を越えると、サーメツトの靭性が低下
して耐欠損性の劣化を招くようになることか
ら、Tiの硬質分散相の金属成分(α+β=1)
に占める割合、すなわちαの値を、原子比で
0.6〜0.9と定めた。
(c) 硬質分散相の組成式におけるβの値
Taも硬質分散相を形成する成分で、Taの含
有によつてサーメツトの耐酸化性が向上するよ
うになるが、その割合が同じく硬質分散相の金
属成分に占める割合(原子比)で0.1未満では
所望の耐酸化性向上効果が得られず、一方その
割合が同0.4を越えると硬質分散相の軟化をも
たらし、サーメツトの耐摩耗性が低下するよう
になることから、Taの硬質分散相の金属成分
に占める割合、すなわちβの値を、原子比で
0.1〜0.4と定めた。
なお、Taの一部を50原子%以下の範囲でNb
で置換してもサーメツトの特性が損なわれるこ
とがないので、Taとの共存においてNbの含有
が許容される。
(d) 硬質分散相の組成式におけるxおよびyの値
C成分およびN成分は共に硬質分散相を構成
する成分であつて、C成分は、硬質分散相の硬
さを向上させ、もつてサーメツトの耐摩耗性を
向上させる作用をもつが、その割合がCおよび
Nの合計(x+y=1)に占める割合(原子
比)で0.50未満では所望のすぐれた耐摩耗性を
確保することができず、一方その割合が同0.90
を越えると、硬質分散相が硬くなりすぎ、サー
メツトの耐欠損性が低下するようになるもので
あり、またN成分は、硬質分散相の粒成長を抑
制して、サーメツトの靭性(耐欠損性)を向上
させる作用をもつが、その割合が同0.10未満で
は所望のすぐれた耐欠損性を確保することがで
きず、一方その割合が同0.50を越えると、サー
メツトの耐摩耗性が低下するようになることか
ら、CおよびN成分の割合、すなわちxおよび
yの値を、それぞれx:0.50〜0.90、y:0.10
〜0.50と定めた。
(e) 硬質分散相の組成式におけるzの値
zの値は、それぞれ硬質分散相を構成するC
およびN成分の合計に対する同金属成分の合計
の割合(原子比)を示すが、その値が0.85未満
では、サーメツトの耐欠損性の低下が著しいの
で、zの下限値を0.85と定めた。なお、zの上
限値が化学量論組成の1.0でもサーメツトの特
性が損なわれることがないので、その上限値を
1.0と定めた。
また、zの値は、主にサーメツト中のN量を
焼結雰囲気の窒素分圧によつて決り、サーメツ
ト中のN量が多く、焼結雰囲気の窒素分圧が低
いほどzの値は小さくなり、この結果サーメツ
トの耐摩耗性は向上するが、反面耐欠損性は低
下するようになるものである。
(f) 硬質分散相の芯部および周辺部の組成
硬質分散相の組成式におけるαおよびβ、並
びにx、y、およびzの値が、それぞれ上記の
条件を満足すると、必然的に芯部の組成が、原
子%で、
Ti:45〜49.5%、
Ta、またはTa+Nb:0.5〜5%、
C:25〜45%、
N:5〜25%、
となり同じく周辺部の組成が、
Ti:25〜45%、
Ta、またはTa+Nb:5〜25%、
C:25〜47.5%、
N:2.5〜15%、
となるものであり、したがつてα、β、x、
y、およびzの値のいずれかでも上記の範囲か
ら外れると、芯部および周辺部の組成は上記の
範囲から外れるようになつて、サーメツトの耐
摩耗性および耐欠損性の少なくともいずれかが
低下するようになるのである。
(g) 結合相の組成
(1) Ti
Ti成分は、結合相の素地に固溶して、サ
ーメツトの耐摩耗性(硬さ)を向上させる作
用をもつが、その含有量が、結合相に占める
割合で0.5%未満では所望の耐摩耗性を確保
することができず、一方その含有量が同割合
で5%を越えると結合相が脆化するようにな
つて、サーメツトの耐欠損性が低下するよう
になることから、その含有量を、結合相に占
める割合(以下同じ)で、0.5〜5%と定め
た。
(2) Ta
Ta成分も結合相に固溶して、サーメツト
の耐酸化性を向上させる作用をもつが、その
含有量が0.1%未満では所望の耐酸化性が得
られず、一方その含有量が3%を越えると、
Tiと同様に結合相に脆化が起り、サーメツ
トの耐欠損性が低下するようになることか
ら、その含有量を0.1〜3%と定めた。
なお、Taの一部が50%以下の範囲でNbで
置換されてもサーメツト特性に変化は現われ
ないので、NbのTaとの共存が許容される。
〔実施例〕
つぎに、この発明のサーメツトを実施例により
具体的に説明する。
原料粉末として、それぞれ第1表に示される組
成を有し、かつ平均粒径が1〜1.5μmの範囲内に
ある各種の炭窒化チタン粉末、同1.1μmのTaC粉
末、同1.0μmのNbC粉末、同2.2μmのNi粉末、お
よび同1.2μmのCo粉末を用意し、これら原料粉
末をそれぞれ第1表に示される配合組成に配合
し、ボールミルにて72時間湿式混合し、乾燥した
後、15Kg/mm2の圧力で圧粉体にプレス成形し、つ
いで、この圧粉体に、10-2torrの真空中で、1330
〜1430℃の範囲内の所定の液相出現温度まで加熱
した後、その雰囲気を3〜10torrの範囲内の所定
の窒素分圧を有する窒素
[Industrial Application Field] This invention has high hardness and high toughness, and exhibits excellent wear resistance and chipping resistance especially when used as a cutting tool, and provides excellent cutting performance over a long period of time. It is related to the performance of cermets. [Conventional technology and its problems] Conventionally, in cermets for cutting tools, the main part of the hard dispersed phase is composed of titanium carbide (hereinafter referred to as TiC), while the main part of the binder phase is composed of either Ni or Co. TiC-based cermets are known that are composed of two or both of these materials, but although these TiC-based cermets have high hardness, they have poor toughness, so they are prone to cracking when used under cutting conditions that require toughness. This makes it impractical for practical use. In addition, in recent years, cermets for cutting tools with high hardness and high toughness have been developed in which the main part of the hard dispersed phase is composed of titanium carbonitride (hereinafter referred to as TiCN).
On the other hand, a TiCN-based cermet in which the main part of the binder phase is similarly composed of either Ni and/or Co has been proposed, but this TiCN-based cermet has poor sinterability and therefore has poor properties. It has large variations and is unreliable. [Means for Solving the Problems] Therefore, from the above-mentioned viewpoints, the present inventors have developed a material that has high hardness and high toughness, has consistent properties, and is excellent when used as a cutting tool. As a result of our research to develop a cermet that exhibits excellent cutting performance, we found TiC powder, tantalum carbide (hereinafter referred to as TaC) powder, niobium carbide (hereinafter referred to as NbC) powder, and two types of these as raw material powders. In addition to the above solid solution powder, titanium nitride (hereinafter referred to as TiN) powder,
Tantalum nitride (hereinafter referred to as TaN) powder, niobium nitride (hereinafter referred to as NbN) powder, Ni powder, and
Co powder is prepared, these raw material powders are blended into a predetermined composition, mixed under normal conditions, and a green compact is press-molded, and then the green compact is placed in a vacuum atmosphere until a liquid phase appears. 0.1~10torr after liquid phase appearance
When sintered in a nitrogen atmosphere with a pressure within the range of , the hard dispersed phase has a cored structure of 70 to 90% by weight. (a) Ti and Ta composite carbonitride; (b) It consists of a composite carbonitride of Ti, Ta and Nb (however, Nb is 50 atomic% or less of Ta), and one of the above (a) and (b), while the remaining 10 to 30% by weight of the binder phase is ,weight%
Contains Ti: 0.5 to 5%, Ta or Ta and Nb (however, Nb is 50% or less of Ta): 0.1 to 3% as a solid solution, and the remainder is Ni and/or Co. When the hard dispersed phase is expressed by the composition formula: {Ti〓(Ta, Nb)〓}(C x N y ) z , the atomic ratio is: , α+β=1, x+y=1, 0.6≦α≦0.9, 0.50≦x≦0.90, 0.1≦β≦0.4, 0.10≦y≦0.50, 0.85≦z≦1.00, and the presence of the above-mentioned hard dispersed phase. The core part that makes up the core structure is
Composition consisting of Ti: 45-49.5%, Ta or Ta and Nb (however, Nb is 50% or less of Ta): 0.5-5%, C: 25-45%, N: 5-25% in atomic percent. On the other hand, the same periphery has the same atomic % Ti: 25-45%, Ta or Ta and Nb (however, Nb is 50% or less of Ta): 5-25%, C: 35-47.5% , N: 2.5-15%, furthermore, the C content is higher in the peripheral area than in the core area, and the N content is higher in the peripheral area than in the core area.
A cermet with a higher concentration distribution in the core than in the periphery can be obtained, and the resulting cermet has high hardness and toughness, as well as good sinterability, so it has good properties. There is no variation in , so when this is used as a cutting tool,
They found that it stably exhibits excellent wear resistance and chipping resistance. This invention has been made based on the above knowledge, and the reasons for the limitations on cermets will be explained below. (a) Content of hard dispersed phase and binder phase The hard dispersed phase has the effect of increasing the hardness of cermet and significantly improving its wear resistance, but its proportion in the cermet is 70% by weight. If the proportion of the binder phase is relatively too large, exceeding 30% by weight, the wear resistance of the cermet will decrease significantly, while if the proportion of the binder phase exceeds 90% by weight, If the proportion of the binder phase is relatively less than 10% by weight, the chipping resistance of the cermet will be significantly reduced, so the proportion thereof was set at 70 to 90% by weight relative to the entire cermet. (b) Value of α in the composition formula of the hard dispersed phase Ti is the main component of the hard dispersed phase, and
It mainly forms the core of the cermet and has the effect of improving the hardness and wear resistance of the cermet, but its proportion (atomic ratio) to the metal components of the hard dispersed phase is less than 0.6. However, if the ratio exceeds 0.9, the toughness of the cermet will decrease and the fracture resistance will deteriorate. Metal component (α+β=1)
In other words, the value of α is expressed as an atomic ratio.
It was set at 0.6 to 0.9. (c) Value of β in the composition formula of the hard dispersed phase Ta is also a component that forms the hard dispersed phase, and the oxidation resistance of cermets is improved by the inclusion of Ta, but the proportion is the same as that of the hard dispersed phase. If the ratio (atomic ratio) to the metal component is less than 0.1, the desired effect of improving oxidation resistance cannot be obtained, while if the ratio exceeds 0.4, the hard dispersed phase will soften and the wear resistance of the cermet will decrease. Therefore, the proportion of Ta in the metal component of the hard dispersed phase, that is, the value of β, can be determined in terms of atomic ratio.
It was set as 0.1 to 0.4. Note that a portion of Ta is replaced with Nb within a range of 50 atomic % or less.
Since the characteristics of the cermet are not impaired even when substituted with Nb, the inclusion of Nb is allowed in coexistence with Ta. (d) Values of x and y in the composition formula of the hard dispersed phase Both the C component and the N component constitute the hard dispersed phase, and the C component improves the hardness of the hard dispersed phase, thereby improving the hardness of the cermet. However, if the ratio (atomic ratio) to the total of C and N (x + y = 1) is less than 0.50, the desired excellent wear resistance cannot be achieved. , while the ratio is 0.90
If it exceeds 100%, the hard dispersed phase becomes too hard and the fracture resistance of the cermet decreases, and the N component suppresses the grain growth of the hard dispersed phase and improves the toughness (fracture resistance) of the cermet. ), but if the ratio is less than 0.10, the desired excellent fracture resistance cannot be secured, while if the ratio exceeds 0.50, the wear resistance of the cermet will decrease. Therefore, the proportions of C and N components, that is, the values of x and y, are x: 0.50 to 0.90, y: 0.10, respectively.
~0.50. (e) Value of z in the compositional formula of the hard dispersed phase The value of z is the C that constitutes the hard dispersed phase.
and the ratio (atomic ratio) of the total of the same metal components to the total of the N components. If the value is less than 0.85, the fracture resistance of the cermet is significantly reduced, so the lower limit of z was set at 0.85. Note that even if the upper limit of z is 1.0, which is the stoichiometric composition, the properties of the cermet will not be impaired.
It was set as 1.0. The value of z is mainly determined by the amount of N in the cermet and the partial pressure of nitrogen in the sintering atmosphere; the larger the amount of N in the cermet and the lower the partial pressure of nitrogen in the sintering atmosphere, the smaller the value of z. As a result, the wear resistance of the cermet is improved, but the chipping resistance is reduced. (f) Composition of the core and periphery of the hard dispersed phase When α and β and the values of x, y, and z in the compositional formula of the hard dispersed phase satisfy the above conditions, the composition of the core and the periphery will inevitably change. The composition is Ti: 45-49.5%, Ta or Ta+Nb: 0.5-5%, C: 25-45%, N: 5-25% in atomic %, and the composition of the peripheral part is Ti: 25-49.5%. 45%, Ta or Ta + Nb: 5 to 25%, C: 25 to 47.5%, N: 2.5 to 15%, and therefore α, β, x,
If any of the values of y and z deviate from the above range, the composition of the core and peripheral parts will deviate from the above range, and at least one of the wear resistance and chipping resistance of the cermet will decrease. They will come to do so. (g) Composition of the binder phase (1) Ti The Ti component is dissolved in the matrix of the binder phase and has the effect of improving the wear resistance (hardness) of cermets, but its content is If the proportion is less than 0.5%, the desired wear resistance cannot be achieved, while if the content exceeds 5%, the binder phase becomes brittle and the fracture resistance of the cermet deteriorates. Therefore, its content was determined to be 0.5 to 5% in proportion to the binder phase (the same applies hereinafter). (2) Ta The Ta component also dissolves in the binder phase and has the effect of improving the oxidation resistance of cermets, but if its content is less than 0.1%, the desired oxidation resistance cannot be obtained; exceeds 3%,
Similar to Ti, the binder phase becomes brittle and the fracture resistance of the cermet decreases, so its content was set at 0.1 to 3%. Note that even if a portion of Ta is replaced by Nb within a range of 50% or less, no change appears in the cermet properties, so the coexistence of Nb and Ta is allowed. [Example] Next, the cermet of the present invention will be specifically explained with reference to Examples. As raw material powders, various titanium carbonitride powders having the compositions shown in Table 1 and having an average particle size within the range of 1 to 1.5 μm, TaC powder with a diameter of 1.1 μm, and NbC powder with a diameter of 1.0 μm are used as raw material powders. , 2.2 μm Ni powder, and 1.2 μm Co powder were prepared, and these raw material powders were blended into the composition shown in Table 1, wet mixed in a ball mill for 72 hours, dried, and then weighed 15 kg. /mm 2 pressure into a green compact, and then this green compact is heated to 1330 mm in a vacuum of 10 -2 torr.
After heating to a predetermined liquid phase appearance temperature in the range of ~1430°C, the atmosphere is replaced with nitrogen having a predetermined nitrogen partial pressure in the range of 3 to 10 torr.
【表】【table】
【表】
雰囲気にかえ、この窒素雰囲気中にて1450〜1500
℃の範囲内の所定の最高温度まで加熱し、この最
高温度に1時間保持の条件で焼結を施すことによ
つて、本発明サーメツト1〜16および比較サーメ
ツト1〜7をそれぞれ製造した。
ついで、この結果得られた本発明サーメツト1
〜16および比較サーメツト1〜7について、通常
の分析方法、並びにE.P.M.A.(電子プローブマイ
クロアナライザー)を用いて、成分組成の分析を
行なつたところ、それぞれ第2表および第3表に
示される結果を示し、かついずれのサーメツトも
硬質分散相が有芯構造を有するものであつた。な
お、硬質分散相の芯部および周辺部の組成は5個
の硬質分散相を測定した結果の平均値で示した。
また、比較サーメツト1〜7は、いずれも組成
がこの発明の範囲から外れたものである。
つぎに、本発明サーメツト1〜16および比較サ
ーメツト1〜7について、耐摩耗性を評価する目
的でロツクウエル硬さ(Aスケール)を、また耐
欠損性(靭性)を評価する目的で抗折力をそれ[Table] 1450 to 1500 in this nitrogen atmosphere instead of the atmosphere
Cermets 1 to 16 of the present invention and Comparative cermets 1 to 7 were produced by heating to a predetermined maximum temperature within the range of 0.degree. C. and sintering under conditions of holding at this maximum temperature for 1 hour. Next, the resulting cermet 1 of the present invention
~16 and comparative cermets 1 to 7 were analyzed for their component compositions using conventional analysis methods and EPMA (electronic probe microanalyzer), and the results are shown in Tables 2 and 3, respectively. The hard dispersed phase of each cermet had a cored structure. In addition, the composition of the core part and the peripheral part of a hard dispersed phase was shown by the average value of the result of measuring five hard dispersed phases. Furthermore, the compositions of Comparative Cermets 1 to 7 are outside the scope of the present invention. Next, for the present invention cermets 1 to 16 and comparative cermets 1 to 7, Rockwell hardness (A scale) was measured for the purpose of evaluating wear resistance, and transverse rupture strength was measured for the purpose of evaluating fracture resistance (toughness). that
【表】
(*印:本発明範囲外)
[Table] (*mark: outside the scope of the present invention)
【表】
ぞれ測定し、さらに、これを切削工具として用
い、
被削材:SNCM439(硬さ:HB260)の丸棒、
切削速度:160m/min、
送り:0.3mm/rev.、
切込み:1.5mm、
切削時間:15mm、
の条件での鋼の連続切削試験、並びに、
被削材:SNCM439(硬さ:HB280)の角材、
切削速度:140m/min、
送り:0.26mm/rev.、
切込み:2mm、
切削時間:3min、
の条件での鋼の断続切削試験を行ない、鋼の連続
切削試験では切刃の逃げ面摩耗幅とすくい面摩耗
深さを測定し、また鋼の断続切削試験では、試験
切刃数:10個のうちの欠損発生切刃数を測定し
た。これらの測定結果を第4表に示した。また、
第4表には、比較の目的で、いずれも市販のTiC
基サーメツト(以下従来サーメツト1という)お
よびTiCN基サーメツト(以下従来サーメツト2[Table] Each was measured and then used as a cutting tool. Work material: SNCM439 (Hardness: H B 260) round bar, Cutting speed: 160m/min, Feed: 0.3mm/rev., Depth of cut. : 1.5mm, Cutting time: 15mm, Continuous cutting test of steel under the conditions, Work material: SNCM439 (hardness: H B 280) square material, Cutting speed: 140m/min, Feed: 0.26mm/rev An interrupted cutting test was conducted on steel under the conditions of ., depth of cut: 2 mm, cutting time: 3 min, and in the continuous cutting test on steel, the flank wear width and rake face wear depth of the cutting edge were measured. In the cutting test, the number of broken cutting edges out of 10 tested cutting edges was measured. The results of these measurements are shown in Table 4. Also,
Table 4 shows commercially available TiC for comparison purposes.
based cermet (hereinafter referred to as conventional cermet 1) and TiCN-based cermet (hereinafter referred to as conventional cermet 2).
第1〜4表に示される結果から明らかなよう
に、本発明サーメツト1〜16は、いずれも高硬度
および高靭性を有し、かつ切削試験では従来サー
メツトに比して一段とすぐれた耐摩耗性と耐欠損
性を示すのに対して、この発明の範囲から外れた
組成を有する比較サーメツト1〜7は、硬さおよ
び靭性のうちの少なくともいずれかが低く、これ
に伴つて切削試験でも劣つた切削結果しか示さな
いものである。
上述のように、この発明のサーメツトは、高硬
度および高靭性を有するので、特にこれらの特性
が要求される切削工具として用いた場合に、著し
く長期に亘つてすぐれた切削性能を発揮するので
ある。
As is clear from the results shown in Tables 1 to 4, the cermets 1 to 16 of the present invention all have high hardness and high toughness, and in the cutting test, they showed much better wear resistance than conventional cermets. On the other hand, comparative cermets 1 to 7 having compositions outside the scope of the present invention had low hardness and/or toughness, and were accordingly inferior in cutting tests. It only shows the cutting results. As mentioned above, the cermet of the present invention has high hardness and high toughness, so it exhibits excellent cutting performance over a long period of time, especially when used as a cutting tool that requires these characteristics. .
Claims (1)
する、TiとTaの複合炭窒化物、またはTiと、
TaおよびNb(ただしNbはTaの50原子%以下)
の複合炭窒化物からなり、 一方、残りの10〜30重量%の結合相が、重量%
で、 Ti:0.5〜5%、 Ta、またはTaとNb(ただしNbはTaの50%以
下):0.1〜3%、 を固溶含有し、残りがNiおよびCoのうちの1種
または2種と不可避不純物からなる組成を有する
合金で構成されたサーメツトにして、 上記硬質分散相を、組成式: {Ti〓(Ta、Nb)〓}(CxNy)z で現わした場合、原子比で、 α+β=1、x+y=1、 0.6≦α≦0.9、0.50≦x≦0.90、 0.1≦β≦0.4、0.10≦y≦0.50、 0.85≦z≦1.00、 を満足すると共に、 上記硬質分散相の有芯構造を構成する芯部は、
原子%で、 Ti:45〜49.5%、 Ta、またはTaとNb(ただしNbはTaの50%以
下):0.5〜5%、 C:25〜45%、 N:5〜25%、 からなる組成を有し、一方同周辺部は、同じく原
子%で、 Ti:25〜45%、 Ta、またはTaとNb(ただしNbはTaの50%以
下):5〜25%、 C:35〜47.5%、 N:2.5〜15%、 からなる組成を有することを特徴とする高硬度お
よび高靭性を有する切削工具用サーメツト。[Claims] 1. A composite carbonitride of Ti and Ta, in which the hard dispersed phase has a cored structure of 70 to 90% by weight, or Ti and
Ta and Nb (however, Nb is less than 50 atomic% of Ta)
of composite carbonitride, while the remaining 10-30% by weight of the binder phase is
Contains Ti: 0.5 to 5%, Ta or Ta and Nb (however, Nb is 50% or less of Ta): 0.1 to 3% as a solid solution, and the remainder is one or two of Ni and Co. When the hard dispersed phase is expressed by the composition formula: {Ti〓(Ta, Nb)〓}(C x N y ) z , atoms In terms of ratio, α+β=1, x+y=1, 0.6≦α≦0.9, 0.50≦x≦0.90, 0.1≦β≦0.4, 0.10≦y≦0.50, 0.85≦z≦1.00, and the above hard dispersed phase The core part that makes up the cored structure of
Composition consisting of Ti: 45-49.5%, Ta or Ta and Nb (however, Nb is 50% or less of Ta): 0.5-5%, C: 25-45%, N: 5-25% in atomic percent. On the other hand, the same periphery has the same atomic % Ti: 25-45%, Ta or Ta and Nb (however, Nb is 50% or less of Ta): 5-25%, C: 35-47.5% , N: 2.5-15%, A cermet for cutting tools having high hardness and high toughness.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP5212085A JPS61213339A (en) | 1985-03-15 | 1985-03-15 | High hardness and high toughness cermet for cutting tool |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP5212085A JPS61213339A (en) | 1985-03-15 | 1985-03-15 | High hardness and high toughness cermet for cutting tool |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS61213339A JPS61213339A (en) | 1986-09-22 |
| JPS634896B2 true JPS634896B2 (en) | 1988-02-01 |
Family
ID=12906013
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP5212085A Granted JPS61213339A (en) | 1985-03-15 | 1985-03-15 | High hardness and high toughness cermet for cutting tool |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS61213339A (en) |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH02131803A (en) * | 1988-11-11 | 1990-05-21 | Mitsubishi Metal Corp | Cutting tool made of abrasion resistant cermet excelling in chipping resistance |
| US5436071A (en) * | 1990-01-31 | 1995-07-25 | Mitsubishi Materials Corporation | Cermet cutting tool and process for producing the same |
-
1985
- 1985-03-15 JP JP5212085A patent/JPS61213339A/en active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| JPS61213339A (en) | 1986-09-22 |
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