JPH08199338A - Coated hard alloy - Google Patents

Coated hard alloy

Info

Publication number
JPH08199338A
JPH08199338A JP7025918A JP2591895A JPH08199338A JP H08199338 A JPH08199338 A JP H08199338A JP 7025918 A JP7025918 A JP 7025918A JP 2591895 A JP2591895 A JP 2591895A JP H08199338 A JPH08199338 A JP H08199338A
Authority
JP
Japan
Prior art keywords
film
hard alloy
oxidation
coated hard
nitride
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
Application number
JP7025918A
Other languages
Japanese (ja)
Other versions
JP3712241B2 (en
Inventor
Hiroshi Ueda
広志 植田
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 JP02591895A priority Critical patent/JP3712241B2/en
Publication of JPH08199338A publication Critical patent/JPH08199338A/en
Application granted granted Critical
Publication of JP3712241B2 publication Critical patent/JP3712241B2/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

Links

Abstract

PURPOSE: To improve the oxidation resistance and oxidation-resisting rate of a coated hard alloy and to enable a long tool service life by specifying the molar ratio of the film compsn. of a coated hard alloy in which a part of a hard film having specified components is substituted with Y. CONSTITUTION: A hard film is formed of the one having 0.5 to 15μm film thickness composed, as the main components, of Ti and Al and/or the nitrides, carbonitrides and carbides of their solid solutions. In the film compsn. of the coated hard alloy in which a part of the same main components is substituted with yttrium is expressed by (Tia Alb Yc )Cx N1-x molar ratios, (a), (b), (c) and (x) respectively satisfy a+b+c=1, 0.3<=a<=0.7, 0.3<=b<=0.7, 0.01<c<=0.20 and 0<=x<=1. Thus, excellent effects can be shown even in the case it is applied to TiCN-base cermet and high speed steel.

Description

【発明の詳細な説明】Detailed Description of the Invention

【0001】[0001]

【産業上の利用分野】本願発明は、耐摩耗性、耐欠損性
に優れる切削工具として用いられる被覆切削工具及び耐
摩耗工具として用いられる被覆耐摩工具に関する。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a coated cutting tool used as a cutting tool having excellent wear resistance and fracture resistance and a coated wear resistant tool used as a wear resistant tool.

【0002】[0002]

【従来の技術】従来PVD法による硬質皮膜は、TiN
が主流であったが、最近TiCN膜あるいは(TiA
l)Nといった新しい種類の皮膜が開発され注目されて
きている。TiCNはビッカース硬さが3000近くあ
り、TiNのビッカース硬さ2200に比べ格段に硬く
耐摩耗性を著しく高める効果も持つ。一方(TiAl)
NはTiとAlの比率により異なるが、概略2300〜
2800のビッカース硬さを有し、TiNに比べ耐摩耗
性を高める一方耐酸化性が優れるため刃先が高温になる
切削条件下などで優れた特性を発揮するものである。
2. Description of the Related Art Conventional hard coatings made by PVD are made of TiN.
Was the mainstream, but recently TiCN film or (TiA
l) A new type of coating such as N has been developed and has been attracting attention. TiCN has a Vickers hardness of about 3000, which is significantly harder than the Vickers hardness of 2200 of TiN, and also has the effect of significantly increasing wear resistance. On the other hand (TiAl)
N varies depending on the ratio of Ti and Al, but is generally 2300
Since it has a Vickers hardness of 2800 and is higher in wear resistance than TiN while being excellent in oxidation resistance, it exhibits excellent characteristics under cutting conditions where the cutting edge has a high temperature.

【0003】又、(TiAl)N膜の皮膜の改善として
Ti/Alの比率を限定した特公平5−67705号
や、(TiAlZr)N、(TiAlV)Nといった更
に多元系の皮膜にした米国特許4871434号等が提
案され、更に改善が計られている。しかしながらこれら
の新しい皮膜は、上述の長所を有するものの耐酸化性に
おいてはまだ十分に満足されるものではない。
Further, in order to improve the film of the (TiAl) N film, Japanese Patent Publication No. 5-67705 in which the ratio of Ti / Al is limited, and further multi-component films such as (TiAlZr) N and (TiAlV) N are used in US patents. No. 4,871,434 has been proposed and further improvements are being made. However, although these new coatings have the above-mentioned advantages, they are not yet sufficiently satisfactory in oxidation resistance.

【0004】[0004]

【発明が解決しようとする課題】その理由は、上述のA
lを含む皮膜は確かに酸化開始温度は、TiN、TiC
Nに比べ高く、耐酸化性には優れるものの酸化が連続的
に進行する条件下においては酸化進行速度は、TiN、
TiCNと比べほとんど変わりのないものである。つま
り、酸化により生成する酸化皮膜は、TiN、TiCN
の場合と同様Alを含有する皮膜においても、ルチル構
造を有し、ポーラスな皮膜である。従って、酸化進行に
対する抵抗は、ルチル構造であるがために極めて低い結
果となるわけである。
The reason for this is the above-mentioned A.
The film containing 1 surely has oxidation start temperatures of TiN and TiC.
Although it is higher than N and has excellent oxidation resistance, the oxidation progress rate is TiN,
It is almost the same as TiCN. That is, the oxide film formed by oxidation is TiN or TiCN.
As in the case of (3), the Al-containing film also has a rutile structure and is a porous film. Therefore, the resistance to the progress of oxidation is extremely low because of the rutile structure.

【0005】[0005]

【本発明の目的】本発明は、TiとAlを含有する窒化
物、炭窒化物皮膜の耐酸化性をさらに改善し、酸化が連
続的に進む高速切削において、より長寿命を示す皮膜を
提供するものである。
The object of the present invention is to further improve the oxidation resistance of nitride and carbonitride coatings containing Ti and Al, and to provide coatings with a longer life in high speed cutting in which oxidation continues. To do.

【0006】[0006]

【課題を解決するための手段】そのため、本発明は(T
iAl)Nを基本にこれに各種元素を添加する検討を行
った結果、Yの添加により耐酸化性が著しく改善される
知見を得た。表1は、3μmの(TiAl)N皮膜をア
ークイオンプレーティング法により、バイアス電圧12
0V、窒素圧力10-1Paの条件下で成膜するときにY
を添加した場合の酸化開始温度、及び850℃大気中で
の酸化速度を、3μmのTiN、(Ti0.5Al0.5)N
皮膜と比較した結果を示す。
Therefore, the present invention provides (T
As a result of investigating addition of various elements to iAl) N based on iAl) N, it was found that the addition of Y significantly improved the oxidation resistance. Table 1 shows that a 3 μm (TiAl) N coating was applied with a bias voltage of 12 by arc ion plating.
Y when forming a film under the conditions of 0 V and a nitrogen pressure of 10 -1 Pa
The starting temperature of the oxidation in the case of adding Al and the oxidation rate in the air at 850 ° C. are 3 μm of TiN and (Ti 0.5 Al 0.5 ) N.
The result compared with the film is shown.

【0007】[0007]

【表1】 [Table 1]

【0008】表1より、(TiAl)N皮膜中にYを固
溶体化させることにより、皮膜の耐酸化性が向上するこ
とがわかる。よって、本願発明は、主成分としてTiと
Al及び/またはその固溶体の窒化物、炭窒化物、炭化
物より構成された0.5〜15μmの膜厚から成る硬質
皮膜の主成分の1部をイットリウムで置換した被覆硬質
合金の該皮膜組成をモル比において、(Tia Alb
c )Cx1-x と表した場合、a、b、c、xがそれぞ
れ、a+b+C=1、0.3≦a≦0.7、0.3≦b
≦0.7、0.01<c≦0.20、0≦x≦1、より
成る膜であり、更に、主成分の一部をYで置換された
(TiAlY)の窒化物、炭窒化物、炭化物の層と、A
lの窒化物または炭窒化物、またはTiの窒化物または
炭窒化物、またはTiAlの固溶体の窒化物または炭窒
化物から成る層を5層以上の多層または積層にして、耐
酸化性・高硬度を達成したものである。
From Table 1, it can be seen that the solid solution of Y in the (TiAl) N coating improves the oxidation resistance of the coating. Therefore, according to the present invention, a part of the main component of the hard coating having a film thickness of 0.5 to 15 μm, which is composed of nitride, carbonitride, and carbide of Ti and Al and / or a solid solution thereof as main components, is yttrium-containing. In the molar ratio, the coating composition of the coated hard alloy substituted with (Ti a Al b Y
c ) When expressed as C x N 1-x , a, b, c and x are respectively a + b + C = 1, 0.3 ≦ a ≦ 0.7, 0.3 ≦ b
≦ 0.7, 0.01 <c ≦ 0.20, 0 ≦ x ≦ 1, and (TiAlY) nitride or carbonitride in which a part of the main component is replaced with Y. , A layer of carbide, A
1 layer of nitride or carbonitride, Ti nitride or carbonitride, or solid solution nitride or carbonitride of TiAl is made into a multi-layer or laminated structure of 5 layers or more to have oxidation resistance and high hardness. Has been achieved.

【0009】[0009]

【作用】上記のように(TiAl)化合物の皮膜中にY
を添加することにより、皮膜の耐酸化性を向上させるこ
とが可能である。特に酸化速度において著しい改善が可
能になる理由は、Yを添加した場合、形成される酸化皮
膜の形態がルチル構造ではなくアナターゼ構造を示すた
めである。つまり、Y添加により非常に緻密な酸化膜が
形成され酸化の進行が形成された酸化膜中の酸素の拡散
に律速される形態をとることにより、酸化の進行が著し
く抑制されるわけである。従って、酸化が連続的に進行
する高速切削において、皮膜の酸化がごく表面のみで発
生し、これが酸化に対し保護膜として作用し、皮膜内部
にまで酸化が進行せず、長寿命が得られるわけである。
[Function] As described above, Y is contained in the (TiAl) compound film.
It is possible to improve the oxidation resistance of the film by adding. In particular, the reason why the oxidation rate can be remarkably improved is that when Y is added, the form of the oxide film formed shows an anatase structure rather than a rutile structure. In other words, the addition of Y forms a very dense oxide film, and the progress of oxidation is controlled by the diffusion of oxygen in the formed oxide film, whereby the progress of oxidation is significantly suppressed. Therefore, in high-speed cutting where oxidation progresses continuously, oxidation of the coating occurs only on the surface, which acts as a protective film against the oxidation and does not progress to the inside of the coating, resulting in long life. Is.

【0010】以下、数値限定した理由に付いて説明す
る。(TiAl)化合物膜中に固溶体/混合体として添
加するYは、0.01以下では耐酸化性を向上するのに
必ずしも十分な効果がなく、0.20を越えると皮膜の
硬さが著しく低下し、著しく劣化する傾向にあるため
0.01<c≦0.20の範囲とした。尚、上記の元素
はターゲット材として固溶体化しても、また各元素を個
別のターゲットとして蒸着時に成分を調整しても、さら
に固溶体ターゲットと個別ターゲットを組み合わせても
同様の効果が得られる。
The reason for limiting the numerical values will be described below. If Y added as a solid solution / mixture in the (TiAl) compound film is 0.01 or less, it is not always sufficient to improve the oxidation resistance, and if it exceeds 0.20, the hardness of the film is remarkably reduced. However, since there is a tendency for remarkable deterioration, the range of 0.01 <c ≦ 0.20 was set. The same effect can be obtained by solidifying the above elements as a target material, adjusting the components during vapor deposition using each element as an individual target, and further combining the solid solution target and the individual target.

【0012】次に、Tiの量は0.7を越えると反対に
Alの含有量が少なくなり、耐酸化性を劣化し0.3未
満であると著しく硬さが低下するため0.3≦a≦0.
7とした。皮膜中のCNの比率は、0≦x≦1、すなわ
ち炭化物、窒化物、炭窒化物の範囲としたのは、(Ti
Al)膜中に固溶体/混合体として添加したYの効果に
より耐酸化性が改善されるため、窒化物よりさらに耐酸
化性の悪い炭化物でも十分に使用でき、また硬さのやや
低い窒化物、炭窒化物においても極端な耐摩耗性の劣化
はないため0≦x≦1の範囲とした。また、多層叉は積
層化については5層以上にしないと個々の層の粒子の微
細化が実現されず、硬さの向上が認められないため5層
以上とした。以下、実施例により本願発明を詳細に説明
する。
Next, when the amount of Ti exceeds 0.7, the content of Al decreases on the contrary, the oxidation resistance deteriorates, and when it is less than 0.3, the hardness is remarkably lowered. a ≦ 0.
It was set to 7. The ratio of CN in the film is 0 ≦ x ≦ 1, that is, the range of carbides, nitrides, and carbonitrides is (Ti
(Al) Since the oxidation resistance is improved by the effect of Y added as a solid solution / mixture in the film, it is possible to sufficiently use a carbide having a poorer oxidation resistance than a nitride, and a nitride having a slightly low hardness, Even in carbonitrides, there is no extreme deterioration in wear resistance, so the range was 0 ≦ x ≦ 1. In addition, if the number of layers or the number of layers is 5 or more, the grain size of the individual layers cannot be reduced and the hardness cannot be improved. Hereinafter, the present invention will be described in detail with reference to Examples.

【0013】[0013]

【実施例1】84WC−3TiC−1TiN−3TaC
−9Coの組成になるよう市販の2.5μmのWC粉
末、1.5μmのTiC粉末、同TiN粉末、1.2μ
mのTaC粉末をボールミルにて96時間混合し、乾燥
造粒の後、SNMG432のTAインサートをプレス
し、焼結後、所定の形状に加工した。この超硬合金基体
上にPVD法により、各種(TiAlY)合金のターゲ
ットを用い、表2に示すような皮膜を形成した。尚、比
較のため従来例で記載した膜も形成した。
Example 1 84WC-3TiC-1TiN-3TaC
Commercially available 2.5 μm WC powder, 1.5 μm TiC powder, same TiN powder, 1.2 μm so as to have a composition of −9 Co.
m TaC powder was mixed in a ball mill for 96 hours, and after dry granulation, the TA insert of SNMG432 was pressed, sintered, and processed into a predetermined shape. The PVD method was used to form the coatings shown in Table 2 on the cemented carbide substrate by using targets of various (TiAlY) alloys. For comparison, the film described in the conventional example was also formed.

【0014】[0014]

【表2】 [Table 2]

【0015】次いで、これらの皮膜をコーティングされ
たスローアウェイインサートを大気中で徐々に昇温し、
酸化増が認められる温度を測定した。また、大気中90
0℃において、時間とともに酸化増量を測定し、酸化速
度を算出した。これらの結果も表2に併記する。更に、
下記に示す高速切削条件にて切削テストを行い最大摩耗
が0.2mmに達するまでの時間を求め、その結果も表
2に併記する。 被削材 S50C (Hs32) 切削速度 300m/min 送り 0.15mm/rev 切込み 1mm 切削油 なし
Then, the throw-away insert coated with these films is gradually heated in the atmosphere,
The temperature at which increased oxidation was observed was measured. In the atmosphere, 90
At 0 ° C., the amount of increased oxidation was measured over time, and the oxidation rate was calculated. These results are also shown in Table 2. Furthermore,
A cutting test was performed under the following high-speed cutting conditions to find the time until the maximum wear reaches 0.2 mm, and the results are also shown in Table 2. Work Material S50C (Hs32) Cutting Speed 300m / min Feed 0.15mm / rev Depth of Cut 1mm No Cutting Oil

【0016】表2より、Yを添加した皮膜は、格段に酸
化速度が遅く、また、そのことが連続高速切削において
著しい長寿命化に寄与している事が明らかである。
From Table 2, it is clear that the coating containing Y has a remarkably slow oxidation rate, and that this contributes to a significantly long life in continuous high-speed cutting.

【0017】[0017]

【実施例2】実施例1で用いた同一の超硬合金スローア
ウェイインサートを用い、表3に示す皮膜成分系の多層
叉は積層化を行った。この場合、皮膜の総厚さは8μm
に統一した。次いで、耐酸化性の評価を実施例1と同様
に行い、その結果を表4に示す。また、ウルトラマイク
ロビッカース(荷重10g)にて硬さの測定を行った結
果も表4に併記する。
Example 2 The same cemented carbide throw-away insert used in Example 1 was used to carry out multilayer or lamination of the coating component system shown in Table 3. In this case, the total thickness of the film is 8 μm
Unified. Next, the oxidation resistance was evaluated in the same manner as in Example 1, and the results are shown in Table 4. In addition, Table 4 also shows the results of measuring the hardness with an ultramicro Vickers (load: 10 g).

【0018】[0018]

【表3】 [Table 3]

【0019】[0019]

【表4】 [Table 4]

【0020】表3より、多層叉は積層化することによ
り、硬さの向上が認められるとともに1600層(1層
当たり5nm)の場合には著しい硬さの向上が認められ
ることが明かである。
From Table 3, it is clear that the improvement of hardness is recognized by the multi-layer or lamination, and the remarkable improvement of hardness is recognized in the case of 1600 layers (5 nm per layer).

【0021】[0021]

【発明の効果】本発明の被覆硬質合金は、従来のTi
N、TiAlNに比べ、Yを添加することにより、耐酸
化性、とりわけ耐酸化速度を向上させ、格段に長い工具
寿命が得られるものである。また、本発明は超硬合金を
主に説明してきたがTiCN基サーメットに適用した場
合、及び高速度鋼に適用した場合にも優れた効果を現す
ことは自明である。
The coated hard alloy of the present invention is the same as the conventional Ti alloy.
By adding Y as compared with N and TiAlN, the oxidation resistance, especially the oxidation resistance rate is improved, and a remarkably long tool life can be obtained. Further, although the present invention has been mainly described for cemented carbide, it is self-evident that it exerts an excellent effect when applied to a TiCN-based cermet and when applied to high speed steel.

Claims (2)

【特許請求の範囲】[Claims] 【請求項1】 主成分としてTiとAl及び/またはそ
の固溶体の窒化物、炭窒化物、炭化物より構成された
0.5〜15μmの膜厚から成る硬質皮膜の主成分の1
部をイットリウムで置換した被覆硬質合金の該皮膜組成
をモル比において、(Tia Albc )Cx1-x
表した場合、a、b、c、xがそれぞれ、a+b+C=
1、0.3≦a≦0.7、0.3≦b≦0.7、0.0
1<c≦0.20、0≦x≦1、より成る膜であること
を特徴とする被覆硬質合金。
1. A main component of a hard coating having a film thickness of 0.5 to 15 μm, which is composed of nitride, carbonitride, and carbide of Ti and Al and / or a solid solution thereof as a main component.
When the coating composition of the coated hard alloy in which the part is replaced by yttrium is expressed as (Ti a Al b Y c ) C x N 1-x in a molar ratio, a, b, c and x are respectively a + b + C =
1, 0.3 ≦ a ≦ 0.7, 0.3 ≦ b ≦ 0.7, 0.0
A coated hard alloy, which is a film consisting of 1 <c ≦ 0.20 and 0 ≦ x ≦ 1.
【請求項2】 請求項1記載の被覆硬質合金において、
主成分の一部をYで置換された(TiAlY)の窒化
物、炭窒化物、炭化物の層と、Alの窒化物または炭窒
化物、またはTiの窒化物または炭窒化物、またはTi
Alの固溶体の窒化物または炭窒化物から成る層を5層
以上の多層または積層にしたことを特徴とする被覆硬質
合金。
2. The coated hard alloy according to claim 1, wherein
A layer of (TiAlY) nitride, carbonitride, or carbide in which a part of the main component is replaced with Y, and a nitride or carbonitride of Al, or a nitride or carbonitride of Ti, or Ti.
A coated hard alloy, characterized in that a layer composed of a nitride or carbonitride of a solid solution of Al is formed into a multilayer or laminated structure of five or more layers.
JP02591895A 1995-01-20 1995-01-20 Coated cutting tool / Coated wear resistant tool Expired - Fee Related JP3712241B2 (en)

Priority Applications (1)

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Application Number Priority Date Filing Date Title
JP02591895A JP3712241B2 (en) 1995-01-20 1995-01-20 Coated cutting tool / Coated wear resistant tool

Publications (2)

Publication Number Publication Date
JPH08199338A true JPH08199338A (en) 1996-08-06
JP3712241B2 JP3712241B2 (en) 2005-11-02

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* Cited by examiner, † Cited by third party
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US7144639B2 (en) * 2002-01-31 2006-12-05 Mitsubishi Materials Corporation Surface-coated cutting tool member having hard coating layer and method for forming the hard coating layer on surface of cutting tool
US7258933B2 (en) 2002-06-25 2007-08-21 Mitsubishi Materials Corporation Coated cutting tool member
JP2007229919A (en) * 2007-04-10 2007-09-13 Oc Oerlikon Balzers Ag Tool having protection layer system
JP2012106299A (en) * 2010-11-16 2012-06-07 Mitsubishi Materials Corp Surface-coated cutting tool
JP2012106297A (en) * 2010-11-16 2012-06-07 Mitsubishi Materials Corp Surface-coated cutting tool
US20150336851A1 (en) * 2012-12-21 2015-11-26 Kabushiki Kaisha Kobe Seiko Sho (Kobe Steel, Ltd.) Hard coating having excellent adhesion resistance to soft metal

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JPH0726381A (en) * 1993-07-12 1995-01-27 Oriental Eng Kk Method for coating surface of substrate and coating member

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US7144639B2 (en) * 2002-01-31 2006-12-05 Mitsubishi Materials Corporation Surface-coated cutting tool member having hard coating layer and method for forming the hard coating layer on surface of cutting tool
CN1325212C (en) * 2002-01-31 2007-07-11 三菱麻铁里亚尔株式会社 Coated cutting tool member having hard coating layer and method for forming the hard coating layer on cutting tool
US7258933B2 (en) 2002-06-25 2007-08-21 Mitsubishi Materials Corporation Coated cutting tool member
JP2007229919A (en) * 2007-04-10 2007-09-13 Oc Oerlikon Balzers Ag Tool having protection layer system
JP2012106299A (en) * 2010-11-16 2012-06-07 Mitsubishi Materials Corp Surface-coated cutting tool
JP2012106297A (en) * 2010-11-16 2012-06-07 Mitsubishi Materials Corp Surface-coated cutting tool
US20150336851A1 (en) * 2012-12-21 2015-11-26 Kabushiki Kaisha Kobe Seiko Sho (Kobe Steel, Ltd.) Hard coating having excellent adhesion resistance to soft metal
US9751809B2 (en) * 2012-12-21 2017-09-05 Kobe Steel, Ltd. Hard coating having excellent adhesion resistance to soft metal

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