JPH10168583A - Coated head alloy - Google Patents
Coated head alloyInfo
- Publication number
- JPH10168583A JPH10168583A JP34675396A JP34675396A JPH10168583A JP H10168583 A JPH10168583 A JP H10168583A JP 34675396 A JP34675396 A JP 34675396A JP 34675396 A JP34675396 A JP 34675396A JP H10168583 A JPH10168583 A JP H10168583A
- Authority
- JP
- Japan
- Prior art keywords
- layer
- hard
- film
- cutting
- coating
- 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
- 239000000956 alloy Substances 0.000 title claims abstract description 14
- 229910045601 alloy Inorganic materials 0.000 title claims abstract description 14
- 150000004767 nitrides Chemical class 0.000 claims abstract description 6
- 239000002184 metal Substances 0.000 claims description 9
- 229910052751 metal Inorganic materials 0.000 claims description 9
- 238000000576 coating method Methods 0.000 abstract description 17
- 239000011248 coating agent Substances 0.000 abstract description 14
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 abstract description 5
- 229910052799 carbon Inorganic materials 0.000 abstract description 3
- -1 carbon nitrides Chemical class 0.000 abstract description 3
- 239000010410 layer Substances 0.000 abstract 6
- CKUAXEQHGKSLHN-UHFFFAOYSA-N [C].[N] Chemical compound [C].[N] CKUAXEQHGKSLHN-UHFFFAOYSA-N 0.000 abstract 2
- 229910052757 nitrogen Inorganic materials 0.000 abstract 2
- 238000010008 shearing Methods 0.000 abstract 2
- 239000000758 substrate Substances 0.000 abstract 2
- PIZYHTQSHRQOBI-UHFFFAOYSA-N [C].O=[N] Chemical class [C].O=[N] PIZYHTQSHRQOBI-UHFFFAOYSA-N 0.000 abstract 1
- 239000011247 coating layer Substances 0.000 abstract 1
- 230000001105 regulatory effect Effects 0.000 abstract 1
- 101150013999 CRBN gene Proteins 0.000 description 3
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 3
- 230000000052 comparative effect Effects 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 101150016677 ohgt gene Proteins 0.000 description 3
- 230000003647 oxidation Effects 0.000 description 3
- 238000007254 oxidation reaction Methods 0.000 description 3
- 230000003746 surface roughness Effects 0.000 description 3
- ZOXJGFHDIHLPTG-UHFFFAOYSA-N Boron Chemical compound [B] ZOXJGFHDIHLPTG-UHFFFAOYSA-N 0.000 description 2
- 229910000831 Steel Inorganic materials 0.000 description 2
- 229910010037 TiAlN Inorganic materials 0.000 description 2
- 238000005299 abrasion Methods 0.000 description 2
- 229910052796 boron Inorganic materials 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 239000013078 crystal Substances 0.000 description 2
- 230000002349 favourable effect Effects 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 238000003801 milling Methods 0.000 description 2
- 230000002040 relaxant effect Effects 0.000 description 2
- 239000010959 steel Substances 0.000 description 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- HSFWRNGVRCDJHI-UHFFFAOYSA-N alpha-acetylene Natural products C#C HSFWRNGVRCDJHI-UHFFFAOYSA-N 0.000 description 1
- LFYJSSARVMHQJB-QIXNEVBVSA-N bakuchiol Chemical compound CC(C)=CCC[C@@](C)(C=C)\C=C\C1=CC=C(O)C=C1 LFYJSSARVMHQJB-QIXNEVBVSA-N 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- 229910001873 dinitrogen Inorganic materials 0.000 description 1
- 230000001814 effect on stress Effects 0.000 description 1
- 125000002534 ethynyl group Chemical group [H]C#C* 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 230000001771 impaired effect Effects 0.000 description 1
- 238000007733 ion plating Methods 0.000 description 1
Landscapes
- Cutting Tools, Boring Holders, And Turrets (AREA)
- Physical Vapour Deposition (AREA)
- Other Surface Treatments For Metallic Materials (AREA)
Abstract
Description
【0001】[0001]
【発明の属する技術分野】本発明は、優れた耐摩耗性を
有する被覆硬質合金に関する。[0001] The present invention relates to a coated hard alloy having excellent wear resistance.
【0002】[0002]
【従来の技術】従来はTiN,TiCN等の皮膜が汎用
的かつ一般的であったが、近年、Alを含有させ耐摩耗
性、耐酸化性を向上させる研究がなされ、特公平4−5
3642号、特公平5−67705号に代表されるよう
に、Alの添加効果を認める事例も種々存在する。しか
しながら、これらの事例は皮膜にAlを添加することに
より、皮膜の耐酸化性、耐摩耗性といった皮膜そのもの
の改善が行われたにすぎない。2. Description of the Related Art Conventionally, films such as TiN and TiCN have been widely and generally used. However, in recent years, studies have been made to improve wear resistance and oxidation resistance by adding Al, and Japanese Patent Publication No. 4-5
As represented by Japanese Patent No. 3642 and Japanese Patent Publication No. 5-67705, there are various cases in which the effect of adding Al is recognized. However, in these cases, the addition of Al to the film merely improves the film itself such as the oxidation resistance and abrasion resistance of the film.
【0003】[0003]
【発明が解決しようとする課題】最近では、切削を高能
率化する傾向が強く、切削速度ならびに切削送りは増加
する傾向にある。このような場合工具寿命を支配する因
子としては、皮膜の耐摩耗性、耐酸化性よりも皮膜の密
着性が極めて重要なものとなる。前記Alを添加した皮
膜は一般に残留圧縮応力が高くその結果、皮膜の密着性
が十分満足されるものでなく、この様な高能率な切削加
工においては、しばしば皮膜が剥離し工具の寿命、信頼
性を損なう結果となっている。従って、この様な高能率
切削においても、長寿命でかつ安定した切削を実現する
ためには、皮膜の密着性をさらに高める必要がある。一
方、密着性を向上させるために、密着性を劣化させる根
本原因である皮膜の残留圧縮応力そのものを低減させる
研究もなされてはいるが、いまだ十分な効果をみるに至
っていないのが現状である。Recently, there has been a strong tendency to increase the efficiency of cutting, and the cutting speed and the cutting feed tend to increase. In such a case, as a factor that governs the tool life, the adhesion of the film is more important than the wear resistance and oxidation resistance of the film. The film to which Al is added generally has a high residual compressive stress, and as a result, the adhesion of the film is not sufficiently satisfied. In such high-efficiency cutting, the film often peels and the life of the tool, reliability The result is a loss of performance. Therefore, even in such high-efficiency cutting, it is necessary to further increase the adhesion of the film in order to realize long-life and stable cutting. On the other hand, in order to improve the adhesion, there has been research on reducing the residual compressive stress itself of the film, which is the root cause of the deterioration of the adhesion, but at present it has not yet seen a sufficient effect. .
【0004】[0004]
【課題を解決するための手段】本発明者らは、皮膜の密
着性を改善すべく鋭意研究を重ねた結果、Alを含有す
る高い圧縮応力を有する皮膜、例えば、TiとAlの窒
化物、炭窒化物、炭窒酸化物、窒硼化物、炭窒硼化物の
一種以上からなる皮膜(「第一の硬質層」)の下に、比
較的に軟らかい皮膜(「第二の硬質層」)を介在させる
ことにより、Alを含有する皮膜の高い圧縮応力は吸収
緩和され結果、皮膜の密着性を著しく改善できる知見を
得るに至った。このことは、皮膜に高い圧縮応力が存在
する場合には、皮膜と基体硬質合金の界面にこの圧縮応
力に起因する高い剪断応力が作用し、この剪断応力が皮
膜の密着性を損なう要因であり、これを緩和、もしくは
除去することが皮膜の密着性を向上させることを示唆す
るものである。つまり、高い圧縮応力を有する皮膜と基
体硬質合金の間に比較的軟らかい層を介在させることに
より、この比較的軟らかい皮膜が高い圧縮応力に起因し
て界面に発生する剪断応力を吸収、緩和したものと考え
られる。Means for Solving the Problems The present inventors have conducted intensive studies to improve the adhesion of the film, and as a result, have found that a film having a high compressive stress containing Al, such as a nitride of Ti and Al, A relatively soft film ("second hard layer") under a film ("first hard layer") composed of one or more of carbonitride, carbonitride, boride and carbonitride By intervening, the high compressive stress of the Al-containing film is absorbed and relaxed, and as a result, it has been found that the adhesion of the film can be remarkably improved. This indicates that, when a high compressive stress is present in the coating, a high shear stress caused by the compressive stress acts on the interface between the coating and the base hard alloy, and this shear stress is a factor that impairs the adhesion of the coating. It is suggested that relaxing or removing this improves the adhesion of the film. In other words, by interposing a relatively soft layer between the film having a high compressive stress and the base hard alloy, the relatively soft film absorbs and relaxes the shear stress generated at the interface due to the high compressive stress. it is conceivable that.
【0005】さらに、本発明者らは研究を重ねた結果、
これらの皮膜の下により軟らかい金属層を介在させるこ
とにより剪断応力をよりいっそう緩和させることができ
る結果を得るに至った。このことはより吸収エネルギー
が高く、またヤング率も低く転位が移動しやすい金属層
が歪みエネルギーを吸収するのにより効果的であること
に基ずく。以上の結果一刃あたりの送り量が0.4mm
を越えるような重断続切削においても、皮膜の剥離は抑
制され、安定した切削加工の実現が可能となった。[0005] Further, as a result of repeated studies by the present inventors,
By interposing a softer metal layer under these coatings, a result was obtained in which the shear stress could be further reduced. This is based on the fact that a metal layer having a higher absorption energy, a lower Young's modulus and a higher dislocation mobility is more effective at absorbing strain energy. As a result, the feed amount per blade is 0.4mm
Even in heavy intermittent cutting, the peeling of the film is suppressed, and stable cutting can be realized.
【0006】また、本発明者らの研究によれば、介在さ
せる皮膜に要求される条件は軟らかいことだけではなく
結晶粒は比較的粗いほうがより応力緩和に好ましく、ま
た面粗さは良いほうが密着性そのものの向上に好ましい
結果となることが明らかとなった。これらの条件を満た
す最適な皮膜(「第二の硬質層」)の一つがCrN,C
rBN等であった。また、硼素(B)の添加により面粗
さが著しく改善され皮膜全体の密着性向上に対しより好
ましい結果をもたらすことが確認された。また、従来T
iN,TiCN,TiC等を介在させる例もみられる
が、本発明者らの研究によればTiN,TiCN,Ti
Cはまず形成される皮膜の面粗さが粗くかつ結晶粒も微
細で剪断応力の吸収、緩和にあまり効果的ではなく、C
rN,CrBN等に較べると皮膜の密着性の改善効果は
著しく低い結果であった。またTiNのようなTiの化
合物はCrNのようなCrの化合物に較べて硬さも硬い
ことも勿論原因の一つである。According to the study of the present inventors, the condition required for the film to be interposed is not only that the film is soft, but that the relatively coarse crystal grains are more preferable for stress relaxation, and the better the surface roughness, the better the adhesion. It has been found that the results are favorable for improving the properties themselves. One of the optimal coatings (“second hard layer”) that meets these conditions is CrN, C
rBN and the like. In addition, it was confirmed that the addition of boron (B) significantly improved the surface roughness and brought about a more favorable result in improving the adhesion of the entire film. Conventional T
In some cases, iN, TiCN, TiC, etc. are interposed, but according to the study of the present inventors, TiN, TiCN, TiC, etc.
C is not very effective in absorbing and relaxing shear stress because the surface roughness of the formed film is coarse and the crystal grains are fine.
As compared with rN, CrBN, etc., the effect of improving the adhesion of the film was remarkably low. Also, one of the reasons is that a Ti compound such as TiN is harder and harder than a Cr compound such as CrN.
【0007】次に数値を限定した理由を述べる。介在さ
せるCrの窒化物層、炭窒化物層、窒硼化物層、炭窒硼
化物層(「第二の硬質層」)の厚さは0.05μm以下
であると応力緩和つまり皮膜の密着性の改善に効果がな
く、5μmを越えるとAlを含む皮膜全体の耐摩耗性を
損なうため0.05μmから5μmとした。また介在さ
せるCr金属層の厚さは5nm以下では同様に応力緩和
つまり皮膜の密着性の改善に効果がなく、500nmを
越えると切削中にこの金属層内で塑性変形が発生し、反
対に皮膜の密着性を損なう結果となるため、5nmから
500nmとした。Next, the reasons for limiting the numerical values will be described. When the thickness of the interposed Cr nitride layer, carbonitride layer, boride layer, and carbonitride layer ("second hard layer") is 0.05 μm or less, stress relaxation, that is, film adhesion When the thickness exceeds 5 μm, the abrasion resistance of the entire film containing Al is impaired, so that the thickness is set to 0.05 μm to 5 μm. When the thickness of the Cr metal layer to be interposed is 5 nm or less, there is no effect on stress relaxation, that is, improvement of the adhesion of the film. When it exceeds 500 nm, plastic deformation occurs in this metal layer during cutting, and conversely, To 5 nm to 500 nm, since this results in a loss of adhesion.
【0008】[0008]
実施例1 小型アークイオンプレーティング装置を用い表1に示す
条件において本発明例、比較例のコーティングを行いコ
ーティッド超硬エンドミルを試作した。硼素はターゲッ
ト金属の中に添加して、この硼素を添加したターゲット
金属を皮膜に添加した。また炭素はアセチレンガスを用
い添加した。TiAlNの膜厚は2.0μmに統一し
た。Example 1 Using a small-sized arc ion plating apparatus, coating was performed on the examples of the present invention and comparative examples under the conditions shown in Table 1, and a coated carbide end mill was prototyped. Boron was added to the target metal, and the boron-added target metal was added to the coating. Carbon was added using acetylene gas. The film thickness of TiAlN was unified to 2.0 μm.
【0009】[0009]
【表1】 [Table 1]
【0010】得られたエンドミルで、以下の切削条件に
て切削テストを行った。 エンドミル φ8mm 6枚刃 被削材 SKD11 HRC60 切削速度 40m/min 送り 0.05mm/刃 切り込み 12mm x 0.8mm 切削 乾式(dry)切削 剥離が発生するまで切削を行った。逃げ面もしくはすく
い面に幅で0.05mm以上の皮膜剥離が発生した時点
の切削長を表1に併記した。A cutting test was performed on the obtained end mill under the following cutting conditions. End mill φ8 mm 6 blades Work material SKD11 HRC60 Cutting speed 40 m / min Feed 0.05 mm / tooth Cutting 12 mm x 0.8 mm Cutting Dry (dry) cutting Cutting was performed until peeling occurred. Table 1 also shows the cutting length at the time when the film flaking of 0.05 mm or more in width occurred on the flank or rake face.
【0011】表1より明らかなように、CrNもしくは
CrBN等を介在させたエンドミルは皮膜の密着性が良
好でHRC60の極めて硬い鋼の切削においても安定な
切削を実現するものである。As is clear from Table 1, the end mill in which CrN or CrBN is interposed has good adhesion of the film and realizes stable cutting even in cutting extremely hard steel of HRC60.
【0012】実施例2 表2に示すコーティング条件でJISP40相当の超硬
インサートに本発明例と比較例のコーティングを行い次
の切削条件にてフライス切削を行い皮膜が剥離するまで
の切削長を求め、表2に併記する。 インサート JIS P40相当 SEE42TN 被削材 SKD61 HRC42 切削速度 160m/min 送り 0.1mm/刃 切り込み 2mm 切削 乾式(dry)切削Example 2 Under the coating conditions shown in Table 2, a carbide insert equivalent to JISP40 was coated according to the present invention and the comparative example, milling was performed under the following cutting conditions, and the cutting length until the coating was peeled was determined. , And Table 2. Insert JIS P40 equivalent SEE42TN Work material SKD61 HRC42 Cutting speed 160m / min Feed 0.1mm / tooth Cutting depth 2mm Cutting Dry (dry) cutting
【0013】[0013]
【表2】 [Table 2]
【0014】表2より明らかなように、CrNもしくは
CrBN等を介在させたインサートは皮膜の密着性が良
好で、HRC42位の高硬度の鋼のミーリング加工にお
いても極めて安定した切削を実現するものである。この
切削例では、皮膜に剥離が発生すると、インサートはす
ぐに欠損に至るため、寿命差が極端に現れている。As is clear from Table 2, the insert with CrN or CrBN or the like has good adhesion of the coating, and realizes extremely stable cutting even in the milling of high hardness steel of HRC42. is there. In this cutting example, if peeling occurs in the coating, the insert immediately breaks, resulting in an extreme difference in service life.
【0015】実施例3 表3に示すコーティング条件にてJIS P40相当の
超硬合金に本発明例並びに比較例に示すコーティングを
行い、表2に示した切削評価を行った。本実施例におい
ても、TiAlNの膜厚は3.0μmとした。また、C
r金属のコーティングにおいては、窒素ガスの導入を止
めて行った。表3に皮膜に剥離が発生し、欠損に至る寿
命までの切削長を併記する。Example 3 Under the coating conditions shown in Table 3, a cemented carbide equivalent to JIS P40 was coated with the coatings shown in Examples of the present invention and Comparative Examples, and the cutting evaluation shown in Table 2 was performed. Also in this example, the thickness of TiAlN was set to 3.0 μm. Also, C
In the coating of r metal, the introduction of nitrogen gas was stopped. Table 3 also shows the cutting length up to the life until the film is peeled off and is broken.
【0016】[0016]
【表3】 [Table 3]
【0017】Cr金属を介在させることにより、いっそ
うの寿命の向上が認められることが明らかである。尚、
コーティング条件は実施例2と同じである。It is clear that the life can be further improved by interposing the Cr metal. still,
The coating conditions are the same as in Example 2.
【0018】[0018]
【発明の効果】本発明により、高能率切削においても、
長寿命でかつ安定した切削を実現することが可能となっ
た。特に、残留圧縮応力の低減により膜が剥離したり、
チッピングが減少したため、正常な摩耗が得られたこと
による。According to the present invention, even in high-efficiency cutting,
Long life and stable cutting can be realized. In particular, the peeling of the film due to the reduction of residual compressive stress,
Normal wear was obtained due to reduced chipping.
フロントページの続き (72)発明者 島 順彦 千葉県成田市新泉13番地の2 日立ツール 株式会社 成田工場内Continued on the front page (72) Inventor Norihiko Shima 13 Shinsen, Narita City, Chiba Prefecture 2 Hitachi Tool Co., Ltd. Narita Factory
Claims (3)
化物、窒硼化物、炭窒硼化物の一種以上からなる第一の
硬質層を基体硬質合金に被覆した被覆硬質合金におい
て、前記第一の硬質層と前記基体硬質合金との間に、C
rの窒化物、炭窒化物、窒硼化物、炭窒硼化物より選ば
れた少なくとも一種の第二の硬質層を介在させたことを
特徴とする被覆硬質合金。1. A coated hard alloy comprising a base hard alloy coated with a first hard layer comprising at least one of a nitride of Ti and Al, a carbonitride, a carbonitride, a boronitride, and a carbonitride. Between the first hard layer and the base hard alloy,
A coated hard alloy comprising at least one second hard layer selected from the group consisting of nitride, carbonitride, boride, and carbonitride.
前記第二の硬質層の層厚が0.05μmから5μmであ
ることを特徴とする被覆硬質合金。2. The coated hard alloy according to claim 1, wherein
The coated hard alloy, wherein the thickness of the second hard layer is 0.05 μm to 5 μm.
いて、前記基体硬質合金と前記第二の硬質層との間に、
層厚で5nmから500nmのCr金属層を介在させた
ことを特徴とする被覆硬質合金。3. The coated hard alloy according to claim 1, wherein between the base hard alloy and the second hard layer,
A coated hard alloy characterized by interposing a Cr metal layer having a thickness of 5 nm to 500 nm.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP34675396A JPH10168583A (en) | 1996-12-10 | 1996-12-10 | Coated head alloy |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP34675396A JPH10168583A (en) | 1996-12-10 | 1996-12-10 | Coated head alloy |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH10168583A true JPH10168583A (en) | 1998-06-23 |
Family
ID=18385586
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP34675396A Pending JPH10168583A (en) | 1996-12-10 | 1996-12-10 | Coated head alloy |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH10168583A (en) |
Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6492011B1 (en) | 1998-09-02 | 2002-12-10 | Unaxis Trading Ag | Wear-resistant workpiece and method for producing same |
JP2005042146A (en) * | 2003-07-25 | 2005-02-17 | Mitsubishi Heavy Ind Ltd | Coating with high abrasion resistance and high hardness |
US7008688B2 (en) | 2001-03-13 | 2006-03-07 | Osg Corporation | Hard multilayer coating, hard multilayer coated tool including the hard multilayer coating, and method of forming the hard multilayer coating |
JP2007063650A (en) * | 2005-09-01 | 2007-03-15 | Osg Corp | Hard stacked film, and hard stacked film-coated tool |
US7217466B2 (en) * | 2002-03-20 | 2007-05-15 | Joerg Guehring | Wear-resistant coating for metal-removing tools, particularly for rotary metal-cutting tools |
WO2020184352A1 (en) * | 2019-03-14 | 2020-09-17 | 三菱マテリアル株式会社 | Surface-coated cutting tool |
-
1996
- 1996-12-10 JP JP34675396A patent/JPH10168583A/en active Pending
Cited By (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6492011B1 (en) | 1998-09-02 | 2002-12-10 | Unaxis Trading Ag | Wear-resistant workpiece and method for producing same |
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JP2005042146A (en) * | 2003-07-25 | 2005-02-17 | Mitsubishi Heavy Ind Ltd | Coating with high abrasion resistance and high hardness |
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