JPH10251832A - Cutting tool made of surface-coated cemented carbide excellent in wear resistance - Google Patents
Cutting tool made of surface-coated cemented carbide excellent in wear resistanceInfo
- Publication number
- JPH10251832A JPH10251832A JP5475897A JP5475897A JPH10251832A JP H10251832 A JPH10251832 A JP H10251832A JP 5475897 A JP5475897 A JP 5475897A JP 5475897 A JP5475897 A JP 5475897A JP H10251832 A JPH10251832 A JP H10251832A
- Authority
- JP
- Japan
- Prior art keywords
- layer
- oxide
- cemented carbide
- cutting tool
- wear resistance
- 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.)
- Granted
Links
Landscapes
- Cutting Tools, Boring Holders, And Turrets (AREA)
- Physical Vapour Deposition (AREA)
Abstract
Description
【0001】[0001]
【発明の属する技術分野】この発明は、すぐれた耐摩耗
性を有し、したがって例えば鋼の連続切削や断続切削で
長期に亘ってすぐれた切削性能を発揮する表面被覆超硬
合金製切削工具(以下、被覆超硬切削工具と云う)に関
するものである。BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a cutting tool made of a surface-coated cemented carbide which has excellent wear resistance and therefore exhibits excellent cutting performance over a long period of time, for example, in continuous cutting and interrupted cutting of steel. Hereinafter, referred to as a coated carbide cutting tool).
【0002】[0002]
【従来の技術】従来、一般に、例えば図1に概略説明図
で示される物理蒸着装置の1種であるアークイオンプレ
ーティング装置を用い、ヒータで装置内を例えば700
℃の温度に加熱した状態で、アノード電極と所定組成を
有するTi−Al合金がセットされたカソード電極(蒸
発源)との間にアーク放電を発生させ、同時に装置内に
反応ガスとして窒素ガス、または窒素ガスとメタンガス
を導入し、一方炭化タングステン(以下、WCで示す)
基超硬合金または炭窒化チタン(以下、TiCNで示
す)基サーメットからなる工具基体(以下、これらを総
称して超硬工具基体と云う)には、例えば−120Vの
バイアス電圧を印加した条件で、前記超硬工具基体の表
面に、例えば特開昭62−56565号公報に記載され
るように、TiとAlの複合窒化物[以下、(Ti,A
l)Nで示す]および複合炭窒化物[以下、(Ti,A
l)CNで示す]のうちの1種の単層または2種の複層
からなる蒸着硬質層で構成された硬質被覆層を0.5〜
15μmの平均層厚で形成することにより被覆超硬切削
工具を製造することが知られている。2. Description of the Related Art Conventionally, for example, an arc ion plating apparatus, which is a kind of physical vapor deposition apparatus schematically shown in FIG.
In the state heated to a temperature of ° C., an arc discharge is generated between the anode electrode and a cathode electrode (evaporation source) on which a Ti-Al alloy having a predetermined composition is set, and at the same time, a nitrogen gas as a reaction gas and Alternatively, nitrogen gas and methane gas are introduced, while tungsten carbide (hereinafter referred to as WC)
A tool base made of a base cemented carbide or a titanium cermet (hereinafter, referred to as TiCN) base cermet (hereinafter, these are collectively referred to as a cemented carbide tool base) are applied under a condition that a bias voltage of -120 V is applied, for example. On the surface of the cemented carbide tool substrate, a composite nitride of Ti and Al [hereinafter, referred to as (Ti, A), as described in, for example, JP-A-62-56565.
l) Indicated by N] and composite carbonitride [hereinafter, (Ti, A
l) Indicated by CN], a hard coating layer composed of a deposited hard layer composed of one kind of single layer or two kinds of multiple layers is 0.5 to
It is known to produce coated carbide cutting tools by forming with an average layer thickness of 15 μm.
【0003】[0003]
【発明が解決しようとする課題】一方、近年の切削加工
のFA化および高速化はめざましく、かつ切削加工の省
力化および省エネ化に対する要求もつよく、これに伴
い、切削工具には使用寿命の延命化が強く望まれている
が、上記の従来被覆超硬切削工具の場合、これを構成す
る硬質被覆層、すなわち(Ti,Al)Nおよび(T
i,Al)CNからなる蒸着硬質層は良好な耐チッピン
グ性(切刃に微小欠けが発生しにくい性質)を示すもの
の、耐摩耗性が十分でないために、比較的短時間で使用
寿命に至るのが現状である。On the other hand, in recent years, FA and speed of cutting have been remarkable, and there is also a demand for labor saving and energy saving of cutting. As a result, the life of cutting tools has been extended. However, in the case of the above-mentioned conventional coated carbide cutting tool, the hard coating layers constituting it, ie, (Ti, Al) N and (T
The deposited hard layer composed of (i, Al) CN shows good chipping resistance (a property that a micro chip is hardly generated in a cutting edge), but has a short wear life and thus has a short service life due to insufficient wear resistance. is the current situation.
【0004】[0004]
【課題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、上記の従来被覆超硬切削工具の
硬質被覆層を構成する(Ti,Al)Nおよび(Ti,
Al)CNからなる蒸着硬質層に着目し、これの耐摩耗
性向上を図るべく研究を行った結果、前記蒸着硬質層
を、 組成式:(Tia Alb Mc )N、 および組成式:(Tia Alb Mc )Cd N1-d 、 (ただし、原子比で、a:0.2〜0.6、b:0.1
〜0.79、c:0.01〜0.3、a+b+c=1、
d:0.01〜0.5を満足し、MはMg、Ca、S
r、およびSiのうちのいずれか1種を示す)、で表さ
れるTiとAlとMの複合窒化物および複合炭窒化物
[以下、それぞれ(Ti,Al,M)Nおよび(Ti,
Al,M)CNで示す]のうちの1種の単層または2種
の複層で構成した上で、これに、減圧下または加圧下の
酸化性雰囲気中、300〜1000℃の範囲内の所定温
度に所定時間保持後、冷却の加熱酸化処理を施すと、被
覆超硬切削工具における上記の(Ti,Al,M)Nお
よび(Ti,Al,M)CNからなる蒸着硬質層が、そ
れぞれTiとAlとMの複合窒酸化物[以下、(Ti,
Al,M)NOで示す]および複合炭窒酸化物[以下、
(Ti,Al,M)CNOで示す]からなる素地に微細
なTi酸化物とAl酸化物とM酸化物が分散分布した組
織を有する加熱酸化層となり、このように硬質被覆層が
前記の加熱酸化層からなる被覆超硬切削工具は、連続切
削および断続切削ですぐれた耐摩耗性を示し、長期に亘
ってすぐれた切削性能を発揮するという研究結果が得ら
れたのである。Means for Solving the Problems Accordingly, the present inventors have
From the above viewpoint, (Ti, Al) N and (Ti, Al) constituting the hard coating layer of the conventional coated carbide cutting tool described above.
Al) focused on deposition hard layer consisting of CN, results of research to achieve this improve wear resistance, the deposited hard layers, the composition formula: (Ti a Al b M c ) N, and the composition formula: (Ti a Al b M c) C d N 1-d, ( provided that an atomic ratio, a: 0.2~0.6, b: 0.1
~ 0.79, c: 0.01 ~ 0.3, a + b + c = 1,
d: 0.01 to 0.5, M is Mg, Ca, S
r, and any one of Si), and a composite nitride and a composite carbonitride of Ti, Al, and M [hereinafter, (Ti, Al, M) N and (Ti,
Al, M) CN], and a single layer or two or more layers of the same, and then, in an oxidizing atmosphere under reduced pressure or pressure, in the range of 300 to 1000 ° C. After holding at a predetermined temperature for a predetermined time and performing cooling heat oxidation treatment, the coated hard layer made of (Ti, Al, M) N and (Ti, Al, M) CN in the coated carbide cutting tool becomes Complex nitride oxide of Ti, Al and M [hereinafter, (Ti,
Al, M) NO] and complex carbonitrides [hereinafter, referred to as
(Shown by (Ti, Al, M) CNO]) on a substrate consisting of a heated oxide layer having a structure in which fine Ti oxide, Al oxide and M oxide are dispersed and distributed. Research results have shown that coated carbide cutting tools comprising an oxide layer exhibit excellent wear resistance in continuous and intermittent cutting and exhibit excellent cutting performance over a long period of time.
【0005】この発明は、上記の研究結果に基づいてな
されたものであって、超硬工具基体の表面に、 組成式:(Tia Alb Mc )N、 および組成式:(Tia Alb Mc )Cd N1-d 、 (ただし、原子比で、a:0.2〜0.6、b:0.1
〜0.79、c:0.01〜0.3、a+b+c=1、
d:0.01〜0.5を満足し、MはMg、Ca、S
r、およびSiのうちのいずれか1種を示す)、で表さ
れる(Ti,Al,M)Nおよび(Ti,Al,M)C
Nのうちの1種の単層または2種の複層からなる蒸着硬
質層の加熱酸化層で構成され、この加熱酸化層の構成層
が、(Ti,Al,M)NOまたは(Ti,Al,M)
CNOからなる素地に微細なTi酸化物とAl酸化物と
M酸化物が分散分布した組織を有する硬質被覆層を、
0.5〜15μmの平均層厚で形成してなる、耐摩耗性
のすぐれた被覆超硬切削工具に特徴を有するものであ
る。[0005] This invention was made based on the above findings, the surface of the cemented carbide tool substrate, the composition formula: (Ti a Al b M c ) N, and the composition formula: (Ti a Al b M c ) C d N 1-d , where a: 0.2 to 0.6, b: 0.1
~ 0.79, c: 0.01 ~ 0.3, a + b + c = 1,
d: 0.01 to 0.5, M is Mg, Ca, S
(Ti, Al, M) N and (Ti, Al, M) C represented by
N is composed of a heat-oxidized layer of a vapor-deposited hard layer composed of one kind of single layer or two or more kinds of N, and the constituent layer of this heat-oxidized layer is (Ti, Al, M) NO or (Ti, Al). , M)
A hard coating layer having a structure in which fine Ti oxide, Al oxide and M oxide are dispersed and distributed on a CNO substrate,
The present invention is characterized by a coated carbide cutting tool having excellent wear resistance and formed with an average layer thickness of 0.5 to 15 μm.
【0006】つぎに、この発明の被覆超硬切削工具の硬
質被覆層にかかる(Ti,Al,M)Nおよび(Ti,
Al,M)CNの組成比(原子比)を上記の通りに限定
した理由を説明する。すなわち、上記(Ti,Al,
M)Nおよび(Ti,Al,M)CNにおいて、構成成
分であるTiとAlは共存した状態で耐摩耗性の向上に
寄与する作用をもつが、TiおよびAlのいずれかでも
Ti:0.2未満およびAl:0.1未満になると所望
のすぐれた耐摩耗性を確保することができず、一方同じ
くTiおよびAlのいずれかでも、その割合がTi:
0.6およびAl:0.79を越えると靭性が低下し、
切刃にチッピングが発生し易くなることから、その割合
をTi:0.2〜0.6、望ましくは0.3〜0.5、
Al:0.1〜0.79、望ましくは0.3〜0.7と
定めた。また、同じく構成成分であるMは、靭性を向上
させ、もって切刃にチッピングが発生するのを防止する
作用をもつが、その割合が0.01未満では所望の靭性
向上効果が得られず、一方その割合が0.3を越えると
層自体の硬さが急激に低下し、TiおよびAlによって
もたらされるすぐれた耐摩耗性を確保することができな
くなることから、その割合を0.01〜0.3、望まし
くは0.05〜0.2と定めた。さらに、(Ti,A
l,M)CNにおけるC成分には、硬さを向上させる作
用があるので、(Ti,Al,M)CNは上記(Ti,
Al,M)Nに比して相対的に高い硬さをもつが、この
場合C成分の割合が0.01未満では所定の硬さ向上効
果が得られず、一方その割合が0.5を越えると靭性が
急激に低下するようになることから、C成分の割合を
0.01〜0.5、望ましくは0.1〜0.45と定め
た。Next, (Ti, Al, M) N and (Ti, M) applied to the hard coating layer of the coated carbide cutting tool of the present invention.
The reason why the composition ratio (atomic ratio) of (Al, M) CN is limited as described above will be described. That is, (Ti, Al,
In (M) N and (Ti, Al, M) CN, the constituent components Ti and Al coexist and have an effect of contributing to the improvement of the wear resistance. If the ratio is less than 2 and Al: less than 0.1, the desired excellent wear resistance cannot be ensured. On the other hand, in the case of either Ti or Al, the proportion is Ti:
When the ratio exceeds 0.6 and Al: 0.79, the toughness decreases,
Since chipping is likely to occur on the cutting edge, the ratio is Ti: 0.2 to 0.6, preferably 0.3 to 0.5,
Al: 0.1 to 0.79, preferably 0.3 to 0.7. Further, M, which is also a component, has an effect of improving toughness and preventing chipping from occurring on the cutting edge, but if the ratio is less than 0.01, a desired effect of improving toughness cannot be obtained. On the other hand, if the ratio exceeds 0.3, the hardness of the layer itself sharply decreases, and it becomes impossible to secure the excellent wear resistance provided by Ti and Al. 0.3, desirably 0.05 to 0.2. Further, (Ti, A
Since the C component in (1, M) CN has an effect of improving the hardness, (Ti, Al, M) CN has the function of (Ti,
Al, M) N has a relatively high hardness as compared with N. In this case, if the proportion of the C component is less than 0.01, a predetermined hardness improving effect cannot be obtained. If it exceeds, the toughness rapidly decreases, so the ratio of the C component is set to 0.01 to 0.5, preferably 0.1 to 0.45.
【0007】また、この発明の被覆超硬切削工具の硬質
被覆層を構成する加熱酸化層の平均層厚を0.5〜15
μmとしたのは、その層厚が0.5μm未満では所望の
耐摩耗性を確保することができず、一方その層厚が15
μmを越えると切刃にチッピングが発生し易くなるとい
う理由からである。さらに、この発明の被覆超硬切削工
具において、これの使用前および使用後の識別を容易に
するために、黄金色を有する窒化チタン(以下、TiN
で示す)層を0.1〜1μmの平均層厚で上記加熱酸化
層の表面に蒸着するとよい。これは、その層厚が0.1
μm未満では黄金色の明確な付与ができず、一方所望の
黄金色は1μmまでの層厚で十分であるという理由によ
るものである。The average thickness of the heat-oxidized layer constituting the hard coating layer of the coated carbide cutting tool of the present invention is 0.5 to 15 mm.
If the layer thickness is less than 0.5 μm, the desired wear resistance cannot be secured, while the layer thickness is 15 μm.
If the thickness exceeds μm, chipping easily occurs on the cutting edge. Further, in the coated carbide cutting tool of the present invention, in order to facilitate identification before and after use, titanium nitride having a golden color (hereinafter referred to as TiN) is used.
It is advisable to deposit a layer on the surface of the heat-oxidized layer with an average layer thickness of 0.1 to 1 μm. This is because the layer thickness is 0.1
If it is less than μm, a clear golden color cannot be imparted, whereas the desired golden color is due to the fact that a layer thickness of up to 1 μm is sufficient.
【0008】[0008]
【発明の実施の形態】ついで、この発明の被覆超硬切削
工具を実施例により具体的に説明する。原料粉末とし
て、いずれも1〜3μmの平均粒径を有するWC粉末、
TiC粉末、ZrC粉末、VC粉末、TaC粉末、Nb
C粉末、Cr3 C2 粉末、TiN粉末、TaN粉末、お
よびCo粉末を用意し、これら原料粉末を、表1に示さ
れる配合組成に配合し、ボールミルで72時間湿式混合
し、乾燥した後、1.5ton/cm2 の圧力で圧粉体
にプレス成形し、この圧粉体を真空中、温度:1400
℃に1時間保持の条件で焼結し、焼結後、切刃部分に
R:0.05のホーニング加工を施してISO規格・S
PGA120408のチップ形状をもったWC基超硬合
金製の超硬工具基体A1〜A8を形成した。また、原料
粉末として、いずれも0.5〜2μmの平均粒径を有す
るTiCN(重量比でTiC/TiN=50/50)粉
末、Mo2 C粉末、ZrC粉末、NbC粉末、TaC粉
末、WC粉末、Co粉末、およびNi粉末を用意し、こ
れら原料粉末を、表2に示される配合組成に配合し、ボ
ールミルで24時間湿式混合し、乾燥した後、1ton
/cm2 の圧力で圧粉体にプレス成形し、この圧粉体を
10torrの窒素雰囲気中、温度:1540℃に1時
間保持の条件で焼結し、焼結後、切刃部分にR:0.0
3のホーニング加工を施してISO規格・CNMG12
0406のチップ形状をもったTiCN基サーメット製
の超硬工具基体B1〜B6を形成した。DESCRIPTION OF THE PREFERRED EMBODIMENTS Next, the coated carbide cutting tool of the present invention will be specifically described with reference to examples. WC powder having an average particle diameter of 1 to 3 μm,
TiC powder, ZrC powder, VC powder, TaC powder, Nb
A C powder, a Cr 3 C 2 powder, a TiN powder, a TaN powder, and a Co powder were prepared, and these raw material powders were blended in the composition shown in Table 1, wet-mixed in a ball mill for 72 hours, and dried. It is pressed into a green compact at a pressure of 1.5 ton / cm 2 , and the green compact is heated in a vacuum at a temperature of 1400.
Sintering under the condition of holding at 1 ° C. for 1 hour.
Carbide tool bases A1 to A8 made of a WC-based cemented carbide having a chip shape of PGA120408 were formed. Further, as raw material powders, TiCN (TiC / TiN = 50/50 by weight ratio) powder, Mo 2 C powder, ZrC powder, NbC powder, TaC powder, WC powder each having an average particle diameter of 0.5 to 2 μm , Co powder, and Ni powder were prepared, and these raw material powders were blended in the blending composition shown in Table 2, wet-mixed in a ball mill for 24 hours, dried, and dried.
/ Cm 2 at a pressure of 1 cm / cm 2 , and sintering the compact in a nitrogen atmosphere of 10 torr for 1 hour at a temperature of 1540 ° C. After sintering, R: 0.0
3 Honing process, ISO standard, CNMG12
Carbide tool bases B1 to B6 made of TiCN-based cermet having a chip shape of No. 0406 were formed.
【0009】ついで、これら超硬工具基体A1〜A8お
よびB1〜B6を、アセトン中で超音波洗浄し、乾燥し
た状態で、それぞれ図1に示されるアークイオンプレー
ティング装置に装入し、一方カソード電極(蒸発源)と
して種々の成分組成をもったTi−Al−M合金を装着
し、装置内を排気して1×10-5torrの真空に保持
しながら、ヒーターで装置内を500℃に加熱した後、
Arガスを装置内に導入して1×10-3torrのAr
雰囲気とし、この状態で超硬工具基体に−800vのバ
イアス電圧を印加して超硬工具基体表面をArガスボン
バート洗浄し、ついで装置内に反応ガスとして窒素ガ
ス、または窒素ガスとメタンガスを導入して5×10-3
torrの反応雰囲気とすると共に、前記超硬工具基体
に印加するバイアス電圧を−200vに下げて、前記カ
ソード電極とアノード電極との間にアーク放電を発生さ
せ、もって前記超硬工具基体A1〜A8およびB1〜B
6のそれぞれの表面に、表3、4に示される組成および
平均層厚をもった蒸着硬質層を形成して被覆超硬工具基
体1〜22とし、さらに引き続いて前記蒸着硬質層形成
の被覆超硬工具基体1〜22のそれぞれに表5に示され
る条件で加熱酸化処理を施して、前記蒸着硬質層をそれ
ぞれ加熱酸化層とすることにより本発明被覆超硬切削工
具1〜22をそれぞれ製造した。また、比較の目的で、
アークイオンプレーティング装置に装着されるカソード
電極(蒸発源)を種々の成分組成をもったTi−Al合
金として、表6、7に示される通りの組成および平均層
厚をもった蒸着硬質層を形成し、この蒸着硬質層に対し
て加熱酸化処理を行わない以外は同一の条件で従来被覆
超硬切削工具1〜22をそれぞれ製造した。なお、この
結果得られた本発明被覆超硬切削工具1〜22のそれぞ
れについて、その加熱酸化層の組織を電子プローブX線
マイクロアナライザー装置およびX線回折装置により観
察したところ、(Ti,Al,M)NOまたは(Ti,
Al,M)CNOからなる素地に微細なTi酸化物とA
l酸化物とM酸化物が分散分布した組織をもつことが確
認された。[0009] Then, these carbide tool bases A1 to A8 and B1 to B6 are ultrasonically cleaned in acetone and dried, and each is charged into an arc ion plating apparatus shown in FIG. Ti-Al-M alloys having various component compositions were mounted as electrodes (evaporation sources), and the inside of the apparatus was evacuated and maintained at a vacuum of 1 × 10 -5 torr while the inside of the apparatus was heated to 500 ° C. After heating,
Ar gas was introduced into the apparatus and 1 × 10 −3 torr of Ar was introduced.
In this state, a bias voltage of -800 V was applied to the cemented carbide tool base to wash the surface of the cemented carbide tool base with Ar gas bombarding. Then, nitrogen gas or nitrogen gas and methane gas were introduced into the apparatus as a reaction gas. 5 × 10 -3
At the same time as the reaction atmosphere of torr, the bias voltage applied to the cemented carbide tool base was reduced to -200 V to generate an arc discharge between the cathode electrode and the anode electrode. And B1 to B
On each surface of No. 6, a deposited hard layer having a composition and an average layer thickness shown in Tables 3 and 4 was formed to obtain coated carbide tool bases 1 to 22, and subsequently, a coated super hard layer formed of the deposited hard layer was formed. Each of the hard tool substrates 1 to 22 was subjected to a heat oxidation treatment under the conditions shown in Table 5, and the coated hard layers were each formed as a heat oxidized layer, thereby producing coated carbide cutting tools 1 to 22 of the present invention. . Also, for comparison purposes,
As the cathode electrode (evaporation source) mounted on the arc ion plating apparatus, a Ti—Al alloy having various component compositions was used, and a deposited hard layer having a composition and an average layer thickness as shown in Tables 6 and 7 was used. The conventional coated carbide cutting tools 1 to 22 were manufactured under the same conditions except that the formed hard layer was not subjected to the heat oxidation treatment. The structure of the heated oxide layer of each of the coated carbide cutting tools 1 to 22 of the present invention obtained as a result was observed with an electron probe X-ray microanalyzer and an X-ray diffractometer. M) NO or (Ti,
Al, M) CNO with fine Ti oxide and A
It was confirmed that 1 oxide and M oxide had a structure in which they were dispersed and distributed.
【0010】この結果得られた各種の被覆超硬切削工具
のうち、本発明被覆超硬切削工具1〜18および従来被
覆超硬切削工具1〜16については、 被削材:JIS・S50Cの角材、 切削速度:300m/min、 送り:0.25mm/刃、 切り込み:2.5mm、 の条件で炭素鋼の乾式フライス切削試験を行ない、また
本発明被覆超硬切削工具17〜22および従来被覆超硬
切削工具17〜22については、 被削材:JIS・SCM440の丸棒、 切削速度:300m/min、 送り:0.2mm/rev、 切り込み:1.5mm、 の条件で合金鋼の乾式連続切削試験を行ない、いずれの
切削試験でも切刃の逃げ面摩耗幅が0.2mmに至るま
での切削時間を測定した。これらの測定結果を表8に示
した。[0010] Of the various coated carbide cutting tools obtained as a result, the coated carbide cutting tools 1 to 18 of the present invention and the conventional coated carbide cutting tools 1 to 16 are as follows: Work material: square material of JIS S50C , Cutting speed: 300 m / min, feed: 0.25 mm / tooth, cutting depth: 2.5 mm, dry milling test of carbon steel was performed, and the coated carbide cutting tools 17 to 22 of the present invention and the conventional coated super For hard cutting tools 17 to 22, Work material: JIS SCM440 round bar, Cutting speed: 300 m / min, Feed: 0.2 mm / rev, Cutting depth: 1.5 mm, Dry continuous cutting of alloy steel under the following conditions: Tests were performed, and in each cutting test, the cutting time until the flank wear width of the cutting edge reached 0.2 mm was measured. Table 8 shows the results of these measurements.
【0011】[0011]
【表1】 [Table 1]
【0012】[0012]
【表2】 [Table 2]
【0013】[0013]
【表3】 [Table 3]
【0014】[0014]
【表4】 [Table 4]
【0015】[0015]
【表5】 [Table 5]
【0016】[0016]
【表6】 [Table 6]
【0017】[0017]
【表7】 [Table 7]
【0018】[0018]
【表8】 [Table 8]
【0019】[0019]
【発明の効果】表1〜8に示される結果から、本発明被
覆超硬切削工具1〜22は、いずれも鋼の連続切削およ
び断続切削(フライス切削)で従来被覆超硬切削工具1
〜22に比してすぐれた耐摩耗性を示すことが明らかで
ある。上述のように、この発明の被覆超硬切削工具は、
硬質被覆層を上記の加熱酸化層で構成することによって
すぐれた耐摩耗性をもつようになり、これによって使用
寿命の著しい延命化が可能となるので、切削加工のFA
化および省力化に十分満足に対応することができるので
ある。From the results shown in Tables 1 to 8, all of the coated carbide cutting tools 1 to 22 according to the present invention are the conventional coated carbide cutting tools 1 in continuous cutting and intermittent cutting (milling) of steel.
It is evident that they show superior wear resistance as compared to # 22. As described above, the coated carbide cutting tool of the present invention
By constituting the hard coating layer with the above-mentioned heat-oxidized layer, it becomes possible to have excellent wear resistance, thereby significantly extending the service life.
It is possible to respond satisfactorily to energy saving and labor saving.
【図1】アークイオンプレーティング装置の概略説明図
である。FIG. 1 is a schematic explanatory view of an arc ion plating apparatus.
───────────────────────────────────────────────────── フロントページの続き (51)Int.Cl.6 識別記号 FI C23C 14/58 C23C 14/58 A ──────────────────────────────────────────────────続 き Continued on the front page (51) Int.Cl. 6 Identification symbol FI C23C 14/58 C23C 14/58 A
Claims (1)
化チタン基サーメットで構成された工具基体の表面に、
硬質被覆層を0.5〜15μmの平均層厚で形成してな
る表面被覆超硬合金製切削工具において、前記硬質被覆
層を、 組成式:(Tia Alb Mc )N、 および組成式:(Tia Alb Mc )Cd N1-d 、 (ただし、原子比で、a:0.2〜0.6、b:0.1
〜0.79、c:0.01〜0.3、a+b+c=1、
d:0.01〜0.5を満足し、MはMg、Ca、S
r、およびSiのうちのいずれか1種を示す)、で表さ
れるTiとAlとMの複合窒化物および複合炭窒化物の
うちの1種の単層または2種の複層からなる蒸着硬質層
の加熱酸化層で構成し、この加熱酸化層の構成層が、T
iとAlとMの複合酸窒化物または炭酸窒化物からなる
素地に微細なTi酸化物とAl酸化物とM酸化物が分散
分布した組織を有することを特徴とする耐摩耗性のすぐ
れた表面被覆超硬合金製切削工具。1. A tool base comprising a tungsten carbide based cemented carbide or a titanium carbonitride based cermet,
In the surface-coated cemented carbide cutting tool obtained by forming a hard coating layer with an average layer thickness of 0.5 to 15 m, the hard coating layer, the composition formula: (Ti a Al b M c ) N, and the composition formula : (Ti a Al b M c ) C d N 1-d, ( provided that an atomic ratio, a: 0.2~0.6, b: 0.1
~ 0.79, c: 0.01 ~ 0.3, a + b + c = 1,
d: 0.01 to 0.5, M is Mg, Ca, S
r, or any one of Si), a single-layer or a double-layer of one of the composite nitrides and carbonitrides of Ti, Al, and M represented by It is composed of a heating oxide layer of a hard layer.
A surface excellent in wear resistance, characterized by having a structure in which fine Ti oxide, Al oxide and M oxide are dispersed and distributed on a substrate made of a composite oxynitride or carbonitride of i, Al and M Coated cemented carbide cutting tool.
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JP05475897A JP3451878B2 (en) | 1997-03-10 | 1997-03-10 | Surface-coated cemented carbide cutting tool with excellent wear resistance |
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JP05475897A JP3451878B2 (en) | 1997-03-10 | 1997-03-10 | Surface-coated cemented carbide cutting tool with excellent wear resistance |
Publications (2)
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JP3451878B2 JP3451878B2 (en) | 2003-09-29 |
Family
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Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US7695829B2 (en) | 2006-09-21 | 2010-04-13 | Kobe Steel, Ltd. | Hard film and hard film-coated tool |
JP2015053357A (en) * | 2013-09-06 | 2015-03-19 | 三菱マテリアル株式会社 | Metal nitride material for thermistors, manufacturing method thereof, and thermistor sensor |
JP5713891B2 (en) * | 2009-05-11 | 2015-05-07 | 昭和電工株式会社 | Catalyst, method for producing the same and use thereof |
-
1997
- 1997-03-10 JP JP05475897A patent/JP3451878B2/en not_active Expired - Fee Related
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US7695829B2 (en) | 2006-09-21 | 2010-04-13 | Kobe Steel, Ltd. | Hard film and hard film-coated tool |
JP5713891B2 (en) * | 2009-05-11 | 2015-05-07 | 昭和電工株式会社 | Catalyst, method for producing the same and use thereof |
US9048499B2 (en) | 2009-05-11 | 2015-06-02 | Showa Denko K.K. | Catalyst, production process therefor and use thereof |
JP2015053357A (en) * | 2013-09-06 | 2015-03-19 | 三菱マテリアル株式会社 | Metal nitride material for thermistors, manufacturing method thereof, and thermistor sensor |
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Publication number | Publication date |
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JP3451878B2 (en) | 2003-09-29 |
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