JPH1161380A - Wear resistant multi-layer type hard coating film - Google Patents
Wear resistant multi-layer type hard coating filmInfo
- Publication number
- JPH1161380A JPH1161380A JP22401397A JP22401397A JPH1161380A JP H1161380 A JPH1161380 A JP H1161380A JP 22401397 A JP22401397 A JP 22401397A JP 22401397 A JP22401397 A JP 22401397A JP H1161380 A JPH1161380 A JP H1161380A
- Authority
- JP
- Japan
- Prior art keywords
- layer
- hardness
- film
- hard coating
- tialn
- 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
Links
- 238000000576 coating method Methods 0.000 title claims abstract description 36
- 239000011248 coating agent Substances 0.000 title claims abstract description 33
- 229910010037 TiAlN Inorganic materials 0.000 claims abstract description 28
- 239000000203 mixture Substances 0.000 claims abstract description 20
- 239000000463 material Substances 0.000 claims abstract description 16
- 239000000126 substance Substances 0.000 claims abstract description 11
- 239000010410 layer Substances 0.000 claims description 53
- 238000000034 method Methods 0.000 claims description 14
- 238000005299 abrasion Methods 0.000 claims description 12
- 239000000758 substrate Substances 0.000 claims description 12
- 239000011247 coating layer Substances 0.000 claims description 2
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 15
- 238000005520 cutting process Methods 0.000 description 15
- 230000000052 comparative effect Effects 0.000 description 9
- 238000007733 ion plating Methods 0.000 description 6
- 230000007423 decrease Effects 0.000 description 4
- 238000005240 physical vapour deposition Methods 0.000 description 4
- 239000002356 single layer Substances 0.000 description 4
- 229910052799 carbon Inorganic materials 0.000 description 3
- 238000005229 chemical vapour deposition Methods 0.000 description 3
- 238000004140 cleaning Methods 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 238000010891 electric arc Methods 0.000 description 3
- 239000007789 gas Substances 0.000 description 3
- 238000004544 sputter deposition Methods 0.000 description 3
- 238000012360 testing method Methods 0.000 description 3
- 229910010038 TiAl Inorganic materials 0.000 description 2
- 229910001315 Tool steel Inorganic materials 0.000 description 2
- 238000013459 approach Methods 0.000 description 2
- 239000012298 atmosphere Substances 0.000 description 2
- 238000011156 evaluation Methods 0.000 description 2
- 229910052757 nitrogen Inorganic materials 0.000 description 2
- 230000003647 oxidation Effects 0.000 description 2
- 238000007254 oxidation reaction Methods 0.000 description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- 229910000997 High-speed steel Inorganic materials 0.000 description 1
- 229910010041 TiAlC Inorganic materials 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- 238000009792 diffusion process Methods 0.000 description 1
- 229910001873 dinitrogen Inorganic materials 0.000 description 1
- 238000005553 drilling Methods 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 150000002500 ions Chemical class 0.000 description 1
- 238000010030 laminating Methods 0.000 description 1
- 238000003754 machining Methods 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 238000003801 milling Methods 0.000 description 1
- 150000004767 nitrides Chemical class 0.000 description 1
- 239000012299 nitrogen atmosphere Substances 0.000 description 1
- 238000005268 plasma chemical vapour deposition Methods 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- 239000002344 surface layer Substances 0.000 description 1
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】本発明は、フライス加工、切
削加工、穿孔加工等の加工に使用される工作工具の表面
コーティング材として有用な耐磨耗性多層型硬質皮膜構
造に関するものである。BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to an abrasion-resistant multilayer hard film structure useful as a surface coating material for a tool used for machining such as milling, cutting and drilling.
【0002】[0002]
【従来の技術】高速度工具鋼や超硬合金工具鋼等を製作
する場合は、耐磨耗性等の性能をより優れたものとする
目的で、工具基材の表面にTi等の窒化物や炭化物より
なる耐磨耗性皮膜を形成することが行なわれている。母
材表面に耐磨耗性皮膜を形成する方法としては、従来よ
りCVD法(化学的蒸着法)およびPVD法(物理的蒸
着法)が知られている。しかし前者の方法では母材が高
温処理に曝される為母材特性が劣化するおそれがあり、
母材特性も重要視される工具の場合は後者の方法が好ま
れる傾向がある。そこで比較的低温条件でコーティング
処理することのできる高周波放電プラズマCVD法、反
応性イオンプレーティング法、スパッタリング法等が採
用されるに至っている。2. Description of the Related Art When manufacturing high-speed tool steel, cemented carbide tool steel, or the like, a nitride such as Ti is coated on the surface of a tool base material for the purpose of improving performance such as wear resistance. Formation of an abrasion resistant film made of carbon or carbide has been performed. As a method for forming a wear-resistant film on the surface of a base material, a CVD method (chemical vapor deposition method) and a PVD method (physical vapor deposition method) are conventionally known. However, in the former method, the base material may be deteriorated because the base material is exposed to the high-temperature treatment.
The latter method tends to be preferred for tools for which the properties of the base material are also important. Therefore, a high-frequency discharge plasma CVD method, a reactive ion plating method, a sputtering method, and the like, which can perform a coating treatment under a relatively low temperature condition, have been adopted.
【0003】工具等の耐磨耗性皮膜としてはイオンプレ
ーティング法によるTiNやTiCが汎用されており、
特に高温耐酸化性(耐熱性)の優れたTiN膜が広く実
用化されている。即ちTiNはTiCより耐熱性に優れ
ている為、切削時の加工熱や摩擦熱によって昇温する工
具すくい面をクレータ磨耗から保護する機能を発揮す
る。しかしTiNはTiCに比べて低硬度である為被削
材と接する逃げ面に発生するフランク磨耗に対してはむ
しろ脆弱であり、フランク磨耗に対してはTiCの方が
高い耐久性を示す。As a wear-resistant film for tools and the like, TiN and TiC by an ion plating method are widely used.
In particular, TiN films excellent in high-temperature oxidation resistance (heat resistance) have been widely put to practical use. That is, since TiN has better heat resistance than TiC, it has a function of protecting the tool rake face, which is heated by processing heat or frictional heat during cutting, from crater wear. However, since TiN has a lower hardness than TiC, it is rather vulnerable to flank wear generated on a flank in contact with a work material, and TiC shows higher durability against flank wear.
【0004】近年、切削速度の一層の高速化が要望され
ており、切削条件がより過酷化する傾向にある為、上記
した様な従来のTiN皮膜程度ではこの要請に応えきれ
なくなっている。そこで耐熱性や硬度が更に優れた皮膜
として、イオンプレーティング法やスパッタリング法に
よるTiAlN,TiAlC,或はTiAlCN等の皮
膜が提案された(特開昭62−56565)。[0004] In recent years, there has been a demand for a higher cutting speed, and cutting conditions tend to be more severe. Therefore, the conventional TiN film as described above cannot meet this demand. Therefore, as a film having even better heat resistance and hardness, a film made of TiAlN, TiAlC, or TiAlCN by an ion plating method or a sputtering method has been proposed (JP-A-62-56565).
【0005】上記のPVD法はイオンのエネルギーを利
用した低温皮膜法であるので、母材表面と皮膜間には、
CVD法において見られた様な熱による拡散層は存在し
ない。従ってPVD法によって形成された皮膜は、CV
D法によって形成された皮膜に比べて密着性が劣るのが
一般的である。一方最近では耐磨耗性を改善して寿命延
長を図るという観点から、皮膜を厚膜化する傾向が見ら
れるが、厚膜化するにつれて皮膜の内部応力が増大し、
皮膜にクラックが発生したり膜密着性が低下して皮膜剥
離の原因になる。尚TiN皮膜に代わり得る高耐磨耗性
皮膜として、(Al,Ti)(N,C)系皮膜が提案さ
れていることは上述した通りであるが、これらの皮膜は
TiN皮膜に比べて内部応力が2倍以上も高くなるの
で、TiN皮膜を形成する場合よりもできるだけ薄い膜
厚を形成して実用されている。こうしたことから、特に
(Al,Ti)(N,C)系皮膜等の優れた特性を十分
に発揮し得る様な、皮膜形成技術の改善が望まれてい
た。[0005] Since the above-mentioned PVD method is a low-temperature film method utilizing the energy of ions, there is a gap between the surface of the base material and the film.
There is no diffusion layer due to heat as seen in the CVD method. Therefore, the film formed by the PVD method is CV
Generally, the adhesion is inferior to the film formed by the method D. On the other hand, recently, from the viewpoint of improving the wear resistance and extending the life, there is a tendency to increase the thickness of the coating, but as the thickness increases, the internal stress of the coating increases,
Cracks occur in the film or film adhesion is reduced, which causes film peeling. As described above, (Al, Ti) (N, C) -based coatings have been proposed as high-abrasion-resistant coatings that can replace the TiN coating. However, these coatings are more internal than the TiN coating. Since the stress is more than twice as high, it is put to practical use by forming a film as thin as possible as compared with the case of forming a TiN film. In view of the above, there has been a demand for an improvement in a film forming technique that can sufficiently exhibit particularly excellent properties such as an (Al, Ti) (N, C) -based film.
【0006】そこで、こうした事情に着目して比較的低
温条件で製膜することができると共に、それにもかかわ
らず、密着性や膜強度に優れ、しかもクレータ磨耗やフ
ランク磨耗に対する抵抗力の優れた耐磨耗性多層型硬質
皮膜を提供した(特開平6−136514)。この皮膜
構成はTiCx N1-x (但し、0≦x≦0.6)で示さ
れる化学組成からなる皮膜層と、(Aly Ti1-y )
(Nz C1-z )(但し、0.56≦y≦0.75、0.
6≦z≦1)で示される化学組成からなる皮膜層が交互
に隣接して、4層以上積層され、かつ全皮膜層厚が0.
6〜12μmである、工具母材表面に形成されるという
ものである。In view of the above circumstances, it is possible to form a film under relatively low temperature conditions by focusing on such circumstances, and nevertheless, it is excellent in adhesion and film strength, and has excellent resistance to crater wear and flank wear. An abrasion-resistant multilayer hard coating was provided (JP-A-6-136514). This coating configuration TiC x N 1-x (where, 0 ≦ x ≦ 0.6) and the film layer made of a chemical composition represented by, (Al y Ti 1-y )
(N z C 1-z ) (provided that 0.56 ≦ y ≦ 0.75, 0.
6 ≦ z ≦ 1), four or more film layers alternately adjacent to each other and having a chemical composition represented by the formula:
It is formed on the surface of the tool base material of 6 to 12 μm.
【0007】上記の耐磨耗性硬質皮膜は、以下の理由に
より耐磨耗性が十分ではなかった。即ち、TiN(x=
0の場合)と(Aly Ti1-y )(Nz C1-z )との積
層ではTiN層部の硬度及び耐酸化性が不足し、TiC
x N1-x (0≦x≦0.6)と(Aly Ti1-y )(N
z C1-z )との積層ではどちらも硬度が高い為、基材と
の密着性や2種類の層間の密着性が不足することが原因
であることを知見した。The abrasion-resistant hard coating described above has not been sufficiently abrasion-resistant for the following reasons. That is, TiN (x =
0) and (Al y Ti 1-y ) (N z C 1-z ), the hardness and oxidation resistance of the TiN layer are insufficient, and TiC
x N 1-x (0 ≦ x ≦ 0.6) and (Al y Ti 1-y) (N
z C 1-z) and for higher even hardness better, stacking, and found that it is due to adhesion of the adhesion and the two layers of the base material is insufficient.
【0008】[0008]
【発明が解決しようとする課題】本発明は上記の問題点
を解決し、皮膜と基材の密着性に優れるとともに、さら
に耐磨耗性に優れた多層型硬質皮膜を提供することを目
的とするものである。SUMMARY OF THE INVENTION An object of the present invention is to solve the above-mentioned problems and to provide a multilayer hard film which is excellent in the adhesion between the film and the substrate and further excellent in abrasion resistance. Is what you do.
【0009】[0009]
【課題を解決するための手段】上記目的を達成し得た発
明とは、工具母材表面に形成される耐磨耗性多層型硬質
皮膜であって、低硬度及び高硬度の2種類のTiAlN
で示される化学組成からなる皮膜が交互に隣接して積層
されたものであり(請求項1)、前記低硬度のTiAl
N層がTi1-x Alx Nにて0.1≦x≦0.4で示さ
れる化学組成からなり、高硬度のTiAlN層がTi
1-x Alx Nにて0.4<x≦0.75で示される化学
組成からなるものであり(請求項2)、前記低硬度のT
iAlN層が、コーティング時の基板バイアス電圧−1
0〜−30Vの条件下で形成され、高硬度のTiAlN
層が基板バイアス電圧−50〜−150Vの条件下で形
成されてなるものであり(請求項3)、前記積層される
単位皮膜層数が10層以上であるものであり(請求項
4)、更に前記低硬度層と高硬度層の厚さ比が5:1〜
1:10である耐磨耗性多層型硬質皮膜である(請求項
5)。The invention which has achieved the above object is an abrasion-resistant multilayer hard coating formed on the surface of a tool base material, comprising two types of TiAlN of low hardness and high hardness.
Wherein the low-hardness TiAl is formed by alternately laminating films having the chemical composition represented by the following formula (1).
The N layer is made of Ti 1-x Al x N and has a chemical composition represented by 0.1 ≦ x ≦ 0.4.
1-x Al x N having a chemical composition represented by 0.4 <x ≦ 0.75 (Claim 2);
The substrate bias voltage at the time of coating-1
TiAlN of high hardness formed under the condition of 0-30V
The layer is formed under the condition of a substrate bias voltage of -50 to -150 V (Claim 3), and the number of the unit film layers to be laminated is 10 or more (Claim 4). Further, the thickness ratio between the low hardness layer and the high hardness layer is 5: 1 to 1
It is a wear-resistant multilayer hard coating having a ratio of 1:10 (claim 5).
【0010】本発明は、非常に高硬度を示すTiAlN
皮膜に、あえて低硬度、すなわち皮膜の内部応力の小さ
いTiAlNをはさみ、積層構造とすることで、皮膜全
体としての内部応力を緩和し、皮膜と基材の密着性が改
善される。また、積層構造とすることで、従来技術同様
に皮膜表層で発生したクラックが、隣接する皮膜層によ
って、その伝播が抑制されることによる耐磨耗性改善効
果が得られるが、特に積層する皮膜がTiAlNで示さ
れる同一の元素構成からなるため、積層皮膜間の密着性
にも非常に優れ、層間での皮膜剥離が減少する。The present invention relates to a TiAlN having a very high hardness.
By intentionally sandwiching TiAlN, which has low hardness, that is, small internal stress of the coating, into the coating to form a laminated structure, the internal stress of the entire coating is relaxed, and the adhesion between the coating and the substrate is improved. Further, by adopting the laminated structure, the cracks generated in the surface layer of the film can be improved by improving the wear resistance by suppressing the propagation of the cracks by the adjacent film layer as in the prior art. Is composed of the same element as TiAlN, so that the adhesion between the laminated films is very excellent, and the peeling of the film between the layers is reduced.
【0011】因みにTiAlNはTiNに比べて高硬度
を示し、一般にAl比率の増加に従って硬度が上昇す
る。そこで通常作成されるTiAlN層に比べ、低Al
組成とすることで低硬度のTiAlN層が形成される。
本発明の効果を発揮させるためには低硬度TiAlN層
のAl組成としてはTi1-x Alx Nにて0.1≦x≦
0.4であり、より好ましくは0.2≦x≦0.3とす
るのが望ましい。x<0.1ではAl添加の効果が得ら
れず、また、x>0.4では硬度が高くなりすぎ、低硬
度層として作用しなくなる。Incidentally, TiAlN has a higher hardness than TiN, and the hardness generally increases as the Al ratio increases. Therefore, compared to a TiAlN layer usually formed, a lower Al
By setting the composition, a low hardness TiAlN layer is formed.
In order to exhibit the effect of the present invention, the Al composition of the low hardness TiAlN layer should be 0.1 ≤ x ≤ Ti 1-x Al x N.
0.4, more preferably 0.2 ≦ x ≦ 0.3. If x <0.1, the effect of adding Al cannot be obtained, and if x> 0.4, the hardness becomes too high, and the layer does not function as a low hardness layer.
【0012】次に高硬度のTiAlN層は、Ti1-x A
lx Nにて0.4<x≦0.75で示されるものが必要
であり、より好ましくは0.6≦x≦0.65とするの
が望ましい。x≦0.4では高硬度層として作用せず、
また、x>0.75でも皮膜層組成がAlNに近似して
くる結果、十分な硬度が得られなくなる。また、一般に
イオンプレーティングやスパッタによって形成されるT
iAlN膜の硬度はコーティング時の基板バイアス電圧
によって大きく影響されることが知られており、バイア
ス電圧を制御することにより低硬度と高硬度のTiAl
N層の作り分けが可能である。Next, the TiAlN layer of high hardness is made of Ti 1-x A
It is necessary that l x N satisfy 0.4 <x ≦ 0.75, more preferably 0.6 ≦ x ≦ 0.65. When x ≦ 0.4, it does not act as a high hardness layer,
Further, even when x> 0.75, the composition of the coating layer approaches AlN, so that sufficient hardness cannot be obtained. In addition, T is generally formed by ion plating or sputtering.
It is known that the hardness of the iAlN film is greatly affected by the substrate bias voltage at the time of coating, and by controlling the bias voltage, low hardness and high hardness TiAl are obtained.
N layers can be separately formed.
【0013】低硬度TiAlN層の形成条件としてはバ
イアス電圧(Vb)が、−30V≦Vb≦−10Vが適
当であり、より好ましくは−20V≦Vb≦−10Vと
するのが望ましい。Vb<−30Vでは低硬度層として
作用しなくなり、またVb>−10Vの場合はアーク放
電プラズマのプラズマ電位に近づくために安定した電圧
印加が難しく、また、0Vバイアスではイオンプレーテ
ィングの効果が得られないため皮膜の特性が悪化する。As a condition for forming the low hardness TiAlN layer, the bias voltage (Vb) is suitably −30 V ≦ Vb ≦ −10 V, more preferably −20 V ≦ Vb ≦ −10 V. When Vb <−30 V, it does not act as a low hardness layer. When Vb> −10 V, it approaches the plasma potential of the arc discharge plasma, making it difficult to apply a stable voltage. Further, at 0 V bias, the effect of ion plating is obtained. The properties of the coating deteriorate.
【0014】また高硬度TiAlN層の形成条件として
は、バイアス電圧を−150V≦Vb≦−50Vの範囲
とするのが適当であり、より好ましくは−100V≦V
b≦−50が望ましい。Vb>−50Vでは高硬度層と
して作用しなくなり、またVb<−150Vでも再度硬
度低下が起こり、高硬度層として作用しなくなる。尚、
本実施例では積層する第1層(低硬度層)と第2層(高
硬度層)でバイアス電圧を不連続に変化させたが、第1
層と第2層の間でのバイアス電圧の変化を勾配を付けて
ある時間で徐々に変化させることも可能である。As a condition for forming the high hardness TiAlN layer, it is appropriate that the bias voltage is in a range of -150 V ≦ Vb ≦ −50 V, and more preferably, −100 V ≦ V
It is desirable that b ≦ −50. When Vb> −50 V, the layer no longer functions as a high hardness layer, and when Vb <−150 V, the hardness decreases again, and the layer does not function as a high hardness layer. still,
In this embodiment, the bias voltage is changed discontinuously between the first layer (low hardness layer) and the second layer (high hardness layer).
It is also possible to gradually change the change in the bias voltage between the layer and the second layer at a certain time with a gradient.
【0015】次に積層される単位皮膜層数が10層以上
であるが、より好ましくは20層以上であり、この際1
0層未満では良好な特性が得られない。本発明では低硬
度層と高硬度層の厚さ比(膜厚比)は5:1〜1:10
(より好ましくは2:1〜1:5)が望ましい。5:1
より外れて低硬度層の比率が高くなると全体の硬度が低
下して耐磨耗性が低下する。また、1:10を越えて高
硬度層の比率が高くなると、全体の硬度が高くなりすぎ
て皮膜の密着性が低下する。[0015] The number of unit film layers to be laminated next is 10 or more, more preferably 20 or more.
If the number is less than 0, good characteristics cannot be obtained. In the present invention, the thickness ratio (thickness ratio) between the low hardness layer and the high hardness layer is 5: 1 to 1:10.
(More preferably 2: 1 to 1: 5). 5: 1
When the ratio of the low hardness layer increases further, the overall hardness decreases and the wear resistance decreases. On the other hand, if the ratio of the high hardness layer exceeds 1:10, the overall hardness becomes too high, and the adhesion of the film decreases.
【0016】[0016]
<実施例1>陰極アーク方式イオンプレーティング装置
にて、自公転可能な基板テーブルを挟んで対向した位置
に取り付けられた少なくとも2つのアーク蒸発源に、T
i1- x Alx (0.1≦x≦0.4)の組成のターゲッ
トとTi0.5 Al0.5 の組成のターゲットを組み込み、
高速度鋼製エンドミル(φ10)へのコーティングを実
施した。<Embodiment 1> At least two arc evaporation sources mounted at positions opposed to each other across a revolving substrate table by a cathodic arc type ion plating apparatus are provided with T
A target having a composition of i 1- x Al x (0.1 ≦ x ≦ 0.4) and a target having a composition of Ti 0.5 Al 0.5 are incorporated,
Coating on a high speed steel end mill (φ10) was performed.
【0017】本発明の多層型硬質皮膜を形成するにあた
っては、まず、装置の真空チャンバを5×10-5Tor
r以下まで真空排気後、ヒータによって基板の加熱を行
う。その後、ガス無し雰囲気中またはArガス雰囲気中
にてアーク放電を発生させ、メタルイオンによる基板の
スパッタクリーニングを行う。クリーニング時はTi
1-x Alx (0.1≦x≦0.4)、Ti0.5 Al0.5
ターゲットのどちらか片方または両方同時に放電させて
良い。クリーニング終了後、チャンバ内を窒素雰囲気に
して、Ti1-x Alx (0.1≦x≦0.4)、Ti
0.5 Al0.5 の両ターゲットにて同時にアーク放電を開
始する。コーティング時の代表的な条件は下記の通りで
ある。In forming the multilayer hard film of the present invention,
First, the vacuum chamber of the device must be 5 × 10-FiveTor
After evacuation to below r, the substrate is heated by a heater.
U. Then, in an atmosphere without gas or in an Ar gas atmosphere
Generates an arc discharge at the
Perform sputter cleaning. Ti for cleaning
1-xAlx(0.1 ≦ x ≦ 0.4), Ti0.5Al0.5
Discharge one or both of the targets simultaneously
good. After cleaning is completed, the inside of the chamber is changed to a nitrogen atmosphere.
And Ti1-xAlx(0.1 ≦ x ≦ 0.4), Ti
0.5Al0.5Arc discharge is simultaneously opened at both targets
Start. Typical conditions for coating are as follows
is there.
【0018】 <コーティング条件> ・窒素ガス圧力:2〜4×10-2Torr(2×10-2Torr…実験条件) ・アーク電流 :80〜200A (100A …実験条件) ・バイアス電圧:−40〜−150V (−50V …実験条件) ・膜厚 :2.5〜3.0μm (実施例もこの範囲程度でばらつき有 り) 上記ガス圧条件下で、基板テーブルを回転させながら、
組成の異なるターゲットを同時に放電させると、各々の
ターゲット前方でターゲット組成に応じた組成のTiA
lN膜が形成され、結果的に組成の異なる2種類のTi
AlN膜が交互に積層された多層型硬質皮膜が形成され
る。回転基板ホルダーの回転数を変化させたり、ターゲ
ットに流すアーク電流を調整することにより、各層の膜
厚を調整することができる。また、ある程度以上各層の
厚みを増すためには、2種類のターゲットを交互に放電
させてもよい。<Coating conditions> Nitrogen gas pressure: 2 to 4 × 10 −2 Torr (2 × 10 −2 Torr: experimental conditions) Arc current: 80 to 200 A (100 A: experimental conditions) Bias voltage: −40 --150 V (-50 V ... experimental conditions)-Film thickness: 2.5-3.0 m (Examples also vary within this range) While rotating the substrate table under the above gas pressure conditions,
When targets having different compositions are simultaneously discharged, TiA having a composition corresponding to the target composition is provided in front of each target.
As a result, two types of Ti having different compositions are formed.
A multilayer hard film in which AlN films are alternately laminated is formed. The film thickness of each layer can be adjusted by changing the rotation speed of the rotating substrate holder or adjusting the arc current flowing through the target. Further, in order to increase the thickness of each layer to a certain extent or more, two types of targets may be alternately discharged.
【0019】上記方法によって各種TiAlN膜を形成
されたエンドミルについて、下記条件での切削試験を行
い、刃先部磨耗量を測定した。 <切削条件> ・被削材 :SKD61(HRC30) ・切削速度:30m/min ・送り :0.07mm/刃 ・切込み :1mm(半径方向),15mm(軸方向) ・切削方法:ダウンカット、エアブロー 切削試験の結果を各皮膜の層構成とともに表1に示す。
尚、表1には比較のためにTiAlN単層、及び従来技
術のTiNとTiAlN層を積層したものを示す。A cutting test was performed on the end mill on which various TiAlN films were formed by the above method under the following conditions, and the amount of wear of the cutting edge was measured. <Cutting conditions>-Work material: SKD61 (HRC30)-Cutting speed: 30 m / min-Feeding: 0.07 mm / blade-Cutting depth: 1 mm (radial direction), 15 mm (axial direction)-Cutting method: down cut, air blow Table 1 shows the results of the cutting test together with the layer structure of each film.
For comparison, Table 1 shows a TiAlN single layer and a laminate of a conventional TiN and TiAlN layer.
【0020】[0020]
【表1】 [Table 1]
【0021】(評価)表1の実施例(No.1〜11)
と比較例(No.12〜15)と比較すると、比較例N
o.12は層数が本発明の特定数より少なく、比較例N
o.13は膜厚比が本発明の特定比を外れており、比較
例No.14はTiAlN膜単層であり、比較例No.
15はTiNとTiAlN積層膜であり、これらの何れ
も実施例の刃先部磨耗量(mm)と比較すると、比較例
のものが劣っており、実施例のものは良好な特性が得ら
れていることが判明している。(Evaluation) Examples of Table 1 (Nos. 1 to 11)
And Comparative Example (Nos. 12 to 15), Comparative Example N
o. In Comparative Example N, the number of layers was smaller than the specific number of the present invention.
o. In Comparative Example No. 13, the film thickness ratio was out of the specific ratio of the present invention. Reference numeral 14 denotes a single layer of a TiAlN film.
Reference numeral 15 denotes a TiN and TiAlN laminated film. When compared with the wear amount (mm) of the cutting edge portion of the example, the comparative example is inferior, and the example has good characteristics. It turns out that.
【0022】<実施例2>低硬度と高硬度のTiAlN
膜の積層は、コーティング時のバイアス電圧を周期的に
変化させることによっても可能である。この場合、各層
の膜厚はバイアス電圧を一定に保持する時間やアーク電
流の増減によって調節可能である。ターゲットとしては
1種類のTi0.5 Al0.5 の組成からなるターゲットを
用いて、各種TiAlN膜を形成したエンドミルについ
て、実施例1と同じ条件での切削試験を行い、刃先部磨
耗量を測定した結果を表2に示す。比較例としてTiA
lN単層、及び従来技術のTiNとTiAlN層を積層
したものも示す。(実施例1と共通)。<Embodiment 2> TiAlN of low hardness and high hardness
Film stacking is also possible by periodically changing the bias voltage during coating. In this case, the thickness of each layer can be adjusted by adjusting the time during which the bias voltage is kept constant or by increasing or decreasing the arc current. Using a target composed of one kind of Ti 0.5 Al 0.5 as a target, a cutting test was performed on the end mill on which various TiAlN films were formed under the same conditions as in Example 1, and the result of measuring the amount of wear of the cutting edge was shown. It is shown in Table 2. TiA as a comparative example
Also shown are a 1N single layer and a stack of prior art TiN and TiAlN layers. (Common with Example 1).
【0023】[0023]
【表2】 [Table 2]
【0024】(評価)表2の実施例(No.1〜5)と
比較例(No.6〜9)と比較すると比較例No.6,
No.7,No.8を比較をする、いずれも第1層バイ
アス電圧は本発明特定外数値であり特に同No.8はT
iAlN膜単層のものであり、比較例No.9はTiN
とTiAlN積層膜のものであり、これらの比較例の何
れも実施例の刃先部磨耗量と比較すると、比較例のもの
が劣っており、実施例のものは良好な特性が得られてい
ることが判明している。(Evaluation) When the examples (Nos. 1 to 5) in Table 2 are compared with the comparative examples (Nos. 6 to 9), the comparative example Nos. 6,
No. 7, No. The first layer bias voltage is a value outside the range specified in the present invention, and particularly, the first layer bias voltage is the same as that of No. 1 in the present invention. 8 is T
It is a single layer of the iAlN film. 9 is TiN
In comparison with the wear amount of the cutting edge of the example, the comparative example is inferior, and that of the example has good characteristics. Is known.
【0025】[0025]
【発明の効果】以上のように本発明は基材の密着性に優
れるとともに耐磨耗性に非常に優れた多層型硬質皮膜が
得られた。As described above, according to the present invention, a multilayer hard film having excellent adhesion to the substrate and very excellent abrasion resistance was obtained.
Claims (5)
型硬質皮膜であって、低硬度及び高硬度の2種類のTi
AlNで示される化学組成からなる皮膜が交互に隣接し
て積層されたことを特徴とする耐磨耗性多層型硬質皮
膜。1. A wear-resistant multilayer hard coating formed on the surface of a tool base material, comprising two types of Ti of low hardness and high hardness.
An abrasion-resistant multilayer hard film, wherein films having a chemical composition represented by AlN are alternately stacked adjacent to each other.
Nにて0.1≦x≦0.4で示される化学組成からな
り、高硬度のTiAlN層がTi1-x Alx Nにて0.
4<x≦0.75で示される化学組成からなる、請求項
1記載の耐磨耗性多層型硬質皮膜。2. The method according to claim 1, wherein the low hardness TiAlN layer is Ti 1-x Al x
N has a chemical composition represented by 0.1 ≦ x ≦ 0.4, and a hard TiAlN layer is formed of Ti 1-x Al x N at 0.1.
The abrasion-resistant multilayer hard coating according to claim 1, comprising a chemical composition represented by the following formula: 4 <x≤0.75.
時の基板バイアス電圧−10〜−30Vの条件下で形成
され、高硬度のTiAlN層が基板バイアス電圧−50
〜−150Vの条件下で形成されてなる請求項1記載の
耐磨耗性多層型硬質皮膜。3. A low-hardness TiAlN layer is formed under a substrate bias voltage of -10 to -30 V during coating, and a high-hardness TiAlN layer is formed at a substrate bias voltage of -50 V.
The abrasion-resistant multilayer hard coating according to claim 1, which is formed under a condition of -150V.
ある、請求項1〜3のいずれかに記載の耐磨耗性多層型
硬質皮膜。4. The wear-resistant multilayer hard coating according to claim 1, wherein the number of unit coating layers to be laminated is 10 or more.
1:10である、請求項1〜3のいずれかに記載の耐磨
耗性多層型硬質皮膜。5. The low-hardness layer and the high-hardness layer have a thickness ratio of 5: 1 to 1.
The wear-resistant multilayer hard coating according to any one of claims 1 to 3, wherein the ratio is 1:10.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP22401397A JPH1161380A (en) | 1997-08-20 | 1997-08-20 | Wear resistant multi-layer type hard coating film |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP22401397A JPH1161380A (en) | 1997-08-20 | 1997-08-20 | Wear resistant multi-layer type hard coating film |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| JPH1161380A true JPH1161380A (en) | 1999-03-05 |
Family
ID=16807228
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP22401397A Pending JPH1161380A (en) | 1997-08-20 | 1997-08-20 | Wear resistant multi-layer type hard coating film |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPH1161380A (en) |
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