JP3016702B2 - Coated hard alloy - Google Patents

Coated hard alloy

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Publication number
JP3016702B2
JP3016702B2 JP7025917A JP2591795A JP3016702B2 JP 3016702 B2 JP3016702 B2 JP 3016702B2 JP 7025917 A JP7025917 A JP 7025917A JP 2591795 A JP2591795 A JP 2591795A JP 3016702 B2 JP3016702 B2 JP 3016702B2
Authority
JP
Japan
Prior art keywords
oxidation
film
carbonitride
nitride
hard alloy
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
JP7025917A
Other languages
Japanese (ja)
Other versions
JPH08199341A (en
Inventor
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 JP7025917A priority Critical patent/JP3016702B2/en
Publication of JPH08199341A publication Critical patent/JPH08199341A/en
Application granted granted Critical
Publication of JP3016702B2 publication Critical patent/JP3016702B2/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

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  • Cutting Tools, Boring Holders, And Turrets (AREA)
  • Physical Vapour Deposition (AREA)

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 chipping resistance, and a coated abrasive 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、(TiA
l)NはTiとAlの比率により異なるが、概略230
0〜2800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。
2. Description of the Related Art Conventionally, a hard film formed by a PVD method is TiN.
Was the mainstream, but recently, TiCN film or (TiA
l) New types of coatings such as N have been developed and attracted attention. TiCN has a Vickers hardness of nearly 3,000, and is much harder than Vickers hardness 2200 of TiN, and also has an effect of significantly increasing wear resistance. On the other hand, (TiA
l) N varies depending on the ratio of Ti to Al, but approximately 230
It has a Vickers hardness of 0 to 2800 and exhibits excellent characteristics under cutting conditions in which the cutting edge is at a high temperature because it has higher abrasion resistance and higher oxidation resistance than TiN.

【0003】また、(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。
In order to improve the film of the (TiAl) N film, Japanese Patent Publication No. Hei 5-67705, in which the ratio of Ti / Al is limited, and US Patents having a more multi-layer film such as (TiAlZr) N and (TiAlV) N No. 4871434 has been proposed and further improvements have been made. However, although these new coatings have the advantages described above, they are still not fully satisfactory in oxidation resistance.

【0004】[0004]

【発明が解決しようとする課題】耐酸化性が不十分な理
由は、上述のAlを含む皮膜は確かに酸化開始温度は、
TiN、TiCN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、T
iN、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、酸化の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 that the oxidation resistance is insufficient is that the above-mentioned film containing Al certainly has an oxidation onset temperature of:
Although it is higher than TiN and TiCN and has excellent oxidation resistance, the oxidation progress rate is almost the same as that of TiN and TiCN under the condition where oxidation proceeds continuously. That is, the oxide film formed by oxidation is T
As in the case of iN and TiCN, the Al-containing coating is a porous coating having a rutile structure. Therefore, the resistance to the progress of oxidation is extremely low due to 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 a coating having a longer life in high-speed cutting where oxidation continues continuously. Is what you do.

【0006】[0006]

【課題を解決するための手段】そのため、本願発明では
(TiAl)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、イットリウム(以後、Yと表記する。)
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(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120V、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3
μmのTiN、(Ti0.5Al0.5)N皮膜と比較した結
果を示す。
Therefore, in the present invention, as a result of studying the addition of various elements based on (TiAl) N, yttrium (hereinafter, referred to as Y) has been studied.
It was found that oxidation resistance was significantly improved by the addition of.
Table 1 shows the oxidation start temperature when Y was added when a 3 μm (TiAl) N film was formed by arc ion plating under the conditions of a bias voltage of 120 V and a nitrogen pressure of 10 −1 Pa, and 850 ° C. Oxidation rate in air is 3
The results are shown in comparison with a μm TiN, (Ti 0.5 Al 0.5 ) N film.

【0007】[0007]

【表1】 [Table 1]

【0008】表1より、(TiAl)N皮膜中にYを添
加することにより、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
Tiの1部をY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、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、0.0
01≦c<0.01、0≦x≦1より成る膜であり、ま
た、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T
iAlの固溶体の窒化物または炭窒化物から成る層を5
層以上の多層叉は積層にし、耐酸化性を高め、かつ高硬
度を達成したものである。
From Table 1, it can be seen that the addition of Y to the (TiAl) N film improves the oxidation resistance of the film. Therefore, in the present invention, a part of Ti of a hard coating having a thickness of 0.5 to 15 μm and composed of nitride, carbonitride, and carbide of Ti and Al and / or a solid solution thereof as a main component is represented by Y. in a molar ratio of said coating composition of substituted coated hard alloy, (Ti a Al b Y c ) when expressed C x N 1-x, a, a, b, c, x, respectively, a + b + C =
1, 0.3 ≦ a ≦ 0.7, 0.3 ≦ b ≦ 0.7, 0.0
A film composed of 01 ≦ c <0.01 and 0 ≦ x ≦ 1; a layer of (TiAlY) nitride, carbonitride, and carbide in which a part of the main component is substituted with Y; Nitride or carbonitride, or Ti nitride or carbonitride, or T
a layer of iAl solid solution nitride or carbonitride
It has a multi-layer structure or a multi-layer structure, which has high oxidation resistance and high hardness.

【0009】[0009]

【作用】(TiAl)化合物の皮膜中にYを添加させる
と、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。
When Y is added to a (TiAl) compound film, the oxidation resistance of the film can be improved. In particular, the reason why a remarkable improvement in the oxidation rate becomes possible is that Y
This is because the form of the formed oxide film shows an anatase structure instead of a rutile structure when is added. That is,
A very dense oxide film is formed by the addition of Y, and the progress of the oxidation is controlled by the diffusion of oxygen in the formed oxide film, whereby the progress of the oxidation is remarkably suppressed. Therefore, in high-speed cutting in which oxidation progresses continuously, oxidation of the film occurs only on the very surface, which acts as a protective film against oxidation, so that oxidation does not progress inside the film and a long life can be obtained. is there.

【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、0.001未満では耐酸化性を向上するの
に十分な効果がなく、0.01を越えると皮膜の硬さが
低下する傾向にあり耐摩耗性が、多少劣化する傾向にあ
るため、0.001≦c<0.01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 to the (TiAl) compound film is less than 0.001, there is no sufficient effect to improve the oxidation resistance, and if it exceeds 0.01, the hardness of the film tends to decrease. Therefore, the abrasion resistance tends to slightly deteriorate, so that the range of 0.001 ≦ c <0.01 is set. still,
Similar effects can be obtained by forming the above-mentioned elements into a solid solution as a target material, adjusting the components at the time of vapor deposition using each element as an individual target, and further combining a solid-solution target and an individual target.

【0011】また、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。
On the other hand, if the content of Ti exceeds 0.7, the content of Al decreases, and the oxidation resistance deteriorates. On the other hand, if it is less than 0.3, the hardness is significantly reduced. ≦ 0.
7 was set. The ratio of CN in the coating was 0 ≦ x ≦ 1, that is, the range of carbide, nitride and carbonitride was (Ti
Al) Oxidation resistance is improved by the effect of Y added as a solid solution / mixture in the film, so that carbides having lower oxidation resistance than nitrides can be used satisfactorily. The range of 0 ≦ x ≦ 1 was set because there is no extreme deterioration in wear resistance of carbonitrides. When the number of layers or the number of layers is not more than five, the size of the particles in each layer cannot be reduced and the hardness is not improved.

【0012】[0012]

【実施例1】以下、実施例により本願発明を詳細に説明
する。84WC−3TiC−1TiN−3TaC−9C
o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、1.2μmのTa
C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PV
D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。
Embodiment 1 Hereinafter, the present invention will be described in detail with reference to embodiments. 84WC-3TiC-1TiN-3TaC-9C
2. A commercially available 2.5 μm WC powder having a composition of
5 μm TiC powder, same TiN powder, 1.2 μm Ta
C 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. PV on the cemented carbide substrate
Films as shown in Table 2 were formed by Method D using various (TiAlY) alloy targets. For comparison, the film described in the conventional example was also formed.

【0013】[0013]

【表2】 [Table 2]

【0014】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。これらの結果を表2に併記した。
Next, the temperature of the throw-away insert coated with these films is gradually increased in the atmosphere,
The temperature at which increased oxidation was observed was measured. In addition, 90
At 0 ° C., the amount of increase in oxidation was measured over time, and the oxidation rate was calculated. These results are shown in Table 2.

【0015】また、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に達するまでの寿命時
間を求め、その結果を表3に示す。
Further, a cutting test was performed under the following high-speed cutting conditions, and a life time until the maximum wear reached 0.2 mm was determined. The results are shown in Table 3.

【0016】[0016]

【表3】 [Table 3]

【0017】表3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 3, it is apparent that the film to which Y is added has a remarkably low oxidation rate, which contributes to a remarkably long life in continuous high-speed cutting.

【0018】[0018]

【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4に示す皮膜成分系の多層
化・積層化を行った。この場合、皮膜の総厚は8μmに
統一して実施した。耐酸化性の試験を実施例1と同様に
行った結果を表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。その結
果も表4に併記する。
Example 2 Using the same cemented carbide indexable insert used in Example 1, the coating component system shown in Table 4 was multilayered and laminated. In this case, the total thickness of the coating was unified to 8 μm. Table 4 shows the results of the oxidation resistance test performed in the same manner as in Example 1. The hardness was measured by Ultra Micro Vickers (load: 10 g). The results are also shown in Table 4.

【0019】[0019]

【表4】 [Table 4]

【0020】表4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。
From Table 4, it is recognized that the hardness is improved by the multilayer or the lamination, and that the hardness is remarkably improved 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 made of a conventional Ti
By adding Y as compared with N and TiAlN, the oxidation resistance, especially the oxidation resistance speed, is improved, and a significantly longer tool life can be obtained. Although the present invention has mainly been described with respect to a cemented carbide, it is obvious that the present invention exhibits excellent effects when applied to a TiCN-based cermet and when applied to a high-speed steel.

Claims (2)

(57)【特許請求の範囲】(57) [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、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、0.0
01≦c<0.01、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 hard coating having a thickness of 0.5 to 15 μm and comprising a nitride, a carbonitride, and a carbide of Ti and Al and / or a solid solution thereof as a main component.
Part of the molar ratio of said coating composition coated hard alloy obtained by substituting yttrium, (Ti a Al b Y c ) when expressed C x N 1-x, a, a, b, c, x, respectively, a + b + C =
1, 0.3 ≦ a ≦ 0.7, 0.3 ≦ b ≦ 0.7, 0.0
A coated hard alloy, characterized in that it is a film comprising 01 ≦ c <0.01 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
以上の多層叉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 a (TiAlY) nitride, carbonitride, or carbide in which a part of the main component is substituted with Y, and a nitride or carbonitride of Al, or a nitride or carbonitride of Ti, or Ti
A coated hard alloy characterized by comprising five or more layers or laminations of a nitride or carbonitride of a solid solution of Al.
JP7025917A 1995-01-20 1995-01-20 Coated hard alloy Expired - Fee Related JP3016702B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP7025917A JP3016702B2 (en) 1995-01-20 1995-01-20 Coated hard alloy

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP7025917A JP3016702B2 (en) 1995-01-20 1995-01-20 Coated hard alloy

Publications (2)

Publication Number Publication Date
JPH08199341A JPH08199341A (en) 1996-08-06
JP3016702B2 true JP3016702B2 (en) 2000-03-06

Family

ID=12179137

Family Applications (1)

Application Number Title Priority Date Filing Date
JP7025917A Expired - Fee Related JP3016702B2 (en) 1995-01-20 1995-01-20 Coated hard alloy

Country Status (1)

Country Link
JP (1) JP3016702B2 (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6060560A (en) 1997-05-23 2000-05-09 Shell Oil Company Polyurethane compositions made from hydroxy-terminated polydiene polymers

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US7033682B1 (en) * 2001-12-28 2006-04-25 Ues, Inc. Coating solutions for titanium and titanium alloy machining
EP2255908A1 (en) 2002-06-25 2010-12-01 Mitsubishi Materials Corporation Coated cutting tool member
AT9999U1 (en) 2007-06-29 2008-07-15 Ceratizit Austria Gmbh AL-TI-RU-N-C HARD COAT LAYER

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6060560A (en) 1997-05-23 2000-05-09 Shell Oil Company Polyurethane compositions made from hydroxy-terminated polydiene polymers

Also Published As

Publication number Publication date
JPH08199341A (en) 1996-08-06

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