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JP2007224374A - Coated member - Google Patents

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JP2007224374A
JP2007224374A JP2006047785A JP2006047785A JP2007224374A JP 2007224374 A JP2007224374 A JP 2007224374A JP 2006047785 A JP2006047785 A JP 2006047785A JP 2006047785 A JP2006047785 A JP 2006047785A JP 2007224374 A JP2007224374 A JP 2007224374A
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aluminum oxide
covering member
layer
outermost layer
coated
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Takashi Ishikawa
剛史 石川
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Moldino Tool Engineering Ltd
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Hitachi Tool Engineering Ltd
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  • Cutting Tools, Boring Holders, And Turrets (AREA)
  • Physical Vapour Deposition (AREA)
  • Drilling Tools (AREA)

Abstract

<P>PROBLEM TO BE SOLVED: To provide a coated member whose coagulation properties and affinity with a workpiece, and chipping resistance are improved, and having excellent wear resistance. <P>SOLUTION: The coated member coated with a hard coating film has the outermost surface layer film-deposited using physical vapor deposition, wherein the outermost surface layer contains aluminum oxide and Nb, and the hard coating film is composed of any of nitride, boride, carbide or oxide comprising two or more kinds selected from Ti, Al, Cr, Si and Nb as metal components of at least one layer different from the outermost surface layer, or their solid solution or mixture. <P>COPYRIGHT: (C)2007,JPO&INPIT

Description

本願発明は、最表層に酸化アルミニウムとNbを含有する被覆部材に関する。   The present invention relates to a covering member containing aluminum oxide and Nb in the outermost layer.

酸化アルミニウム皮膜を最表層とした被覆工具の技術が特許文献1に開示されている。また、物理蒸着法により酸化アルミニウムなどの酸化物皮膜を被覆する技術が特許文献2、3に開示されている。   Patent Document 1 discloses a technique of a coated tool having an aluminum oxide film as an outermost layer. Patent Documents 2 and 3 disclose techniques for coating an oxide film such as aluminum oxide by physical vapor deposition.

特開2005−262356号公報JP 2005-262356 A 特開平5−57507号公報JP-A-5-57507 特開2005−138210号公報JP 2005-138210 A

特許文献1は、耐熱性に優れ、靭性と耐摩耗性を有する被覆工具として、固体蒸着源を用いて成膜した酸化物層を用いる技術を開示している。酸化物層の面粗さRmax値は、0.3μm未満とし、また酸化物層は、Al、Zr、Si、Cr、Ti、Bから選択される元素を含有することが記載されている。しかし、酸化物層の面粗さRmax値は、最表面の値ではなく、被覆層断面から測定した値によって規定している。また被加工物との耐凝着性、耐溶着性についての改善は配慮されていない。特許文献2は、工具刃先部の耐溶着性を改善する目的で、最外層を酸化アルミニウム膜で構成し、面粗さRaが0.4μm以下、工具刃先部を研磨加工で処理する技術を開示している。特許文献3の被覆切削工具は、被覆層が内層、外層を有し、内層は硬質皮膜、外層は酸化アルミニウムで構成する技術を開示している。酸化アルミニウムの一部は非晶質で圧縮応力を有し、物理蒸着法により被覆された被覆切削工具である。しかし、特許文献2、3の物理蒸着法により被覆された酸化アルミニウムは、結晶粒子が粗大であり、且つ突起状の形状を有しているため、その優れた特性を発揮する前に、結晶粒子の脱落や突起状を有した結晶粒子に被加工物が付着することにより、剥離や異常摩耗が発生する等の問題がある。
そこで本願発明の目的は、被加工物との凝着性、親和性及び耐欠損性を改善し、優れた耐摩耗性を有する被覆部材を提供することである。
Patent Document 1 discloses a technique in which an oxide layer formed using a solid deposition source is used as a coated tool having excellent heat resistance and toughness and wear resistance. It is described that the surface roughness Rmax value of the oxide layer is less than 0.3 μm, and the oxide layer contains an element selected from Al, Zr, Si, Cr, Ti, and B. However, the surface roughness Rmax value of the oxide layer is defined not by the value of the outermost surface but by the value measured from the cross section of the coating layer. In addition, improvement in adhesion resistance and adhesion resistance with the workpiece is not considered. Patent Document 2 discloses a technique in which the outermost layer is made of an aluminum oxide film, the surface roughness Ra is 0.4 μm or less, and the tool edge part is processed by polishing for the purpose of improving the welding resistance of the tool edge part. is doing. The coated cutting tool of Patent Document 3 discloses a technique in which a coating layer has an inner layer and an outer layer, the inner layer is formed of a hard coating, and the outer layer is formed of aluminum oxide. A part of aluminum oxide is a coated cutting tool which is amorphous and has compressive stress and is coated by physical vapor deposition. However, the aluminum oxide coated by the physical vapor deposition method of Patent Documents 2 and 3 has coarse crystal grains and has a protruding shape. There is a problem that peeling or abnormal wear occurs due to the work piece adhering to the crystal grains having a drop-off or protruding shape.
SUMMARY OF THE INVENTION Accordingly, an object of the present invention is to provide a covering member that improves adhesion, affinity, and fracture resistance with a workpiece and has excellent wear resistance.

本願発明の被覆部材は、物理蒸着を用いて成膜された最表層を有し、該最表層は酸化アルミニウムとNbを含有することを特徴とする被覆部材である。上記の構成を採用することによって、被加工物との凝着性、親和性及び耐欠損性を改善し、優れた耐摩耗性を有する被覆部材を提供することが可能となる。   The covering member of the present invention is a covering member having an outermost layer formed by physical vapor deposition, and the outermost layer contains aluminum oxide and Nb. By adopting the above configuration, it is possible to improve the adhesion, affinity, and fracture resistance with the workpiece and to provide a covering member having excellent wear resistance.

本願発明の被覆部材の最表層は、Nbの1部をTi、Cr、Si、B、から選択される1種以上で置換することが好ましい。最表層とは異なる別の少なくとも1層が、金属成分として、Ti、Al、Cr、Si、Nbから選択される2種以上を含有する窒化物、ホウ化物、炭化物及び酸化物の何れか又はそれらの固溶体又は混合物からなる硬質皮膜を具えることが好ましい。また、本願発明の被覆部材は、該最表層の面粗さRa、Ryが(μm)で、Ra≦0.03、Ry≦0.5、であり、最表層を機械的処理により平滑にすることが有効である。   In the outermost layer of the covering member of the present invention, it is preferable to substitute one part of Nb with one or more selected from Ti, Cr, Si, and B. At least one layer different from the outermost layer is any one of nitride, boride, carbide and oxide containing two or more selected from Ti, Al, Cr, Si, and Nb as a metal component, or those It is preferable to provide a hard film comprising a solid solution or a mixture of the above. In the covering member of the present invention, the surface roughness Ra, Ry of the outermost layer is (μm), Ra ≦ 0.03, Ry ≦ 0.5, and the outermost layer is smoothed by mechanical treatment. It is effective.

本願発明により、被加工物との凝着性、親和性及び耐欠損性を改善し、優れた耐摩耗性を有する被覆部材を提供することができた。   According to the present invention, it was possible to provide a covering member having improved wear resistance, affinity and fracture resistance with a workpiece, and having excellent wear resistance.

本願発明の被覆部材の最表層に、酸化アルミニウムとNbを含有することによって、被加工物との凝着性、親和性及び耐欠損性を改善し、優れた耐摩耗性を有する。Nbの含有量は原子%で、0.1%から30%の範囲であることが好ましい。この理由として、酸化アルミニウムにNbが0.1%から30%の範囲で含有する場合、結晶粒径を微細化する効果のあることが考えられる。酸化アルミニウム皮膜表面の面粗さを小さい状態に制御することによって、被加工物の凝着を減少させることが可能となる。更に、摩耗特性を改善することができる。酸化アルミニウムの結晶粒径を微細化することで、表面を平滑にして、被加工物との凝着性、親和性及び耐欠損性を改善した。一方、Nbが0.1%未満では、結晶粒径を微細化の効果を得ることができない。また、30%を超えると酸化アルミニウム皮膜の耐摩耗性が劣るため、不都合である。本願発明の被覆は、物理蒸着(以下、PVDと記す。)であることが好ましい。この理由は、皮膜に圧縮残留応力を付与することができるからである。好ましいPVDは、スパッタリング、アーク放電式イオンプレーティング(以下、AIPと記す。)がある。各種元素の添加には、PVDによる場合、予め添加元素であるNbを含有した金属ターゲット材を準備しておくことによって、容易に酸化アルミニウム皮膜に添加することができる。即ち、酸化アルミニウムターゲットを装着した蒸着源1と、添加元素を含有した金属ターゲットを装着した蒸着源2とが真空装置内で同時に稼動することより、元素添加が可能である。酸化アルミニウム皮膜の結晶構造は、α型、γ型、κ型、非晶質相が挙げられる。これらの何れかまたは混在する場合においても本願発明の効果が得られる。好ましい結晶構造は、α型酸化アルミニウムである。   By containing aluminum oxide and Nb in the outermost layer of the covering member of the present invention, adhesion to the workpiece, affinity, and fracture resistance are improved, and excellent wear resistance is achieved. The Nb content is atomic%, preferably in the range of 0.1% to 30%. The reason is considered that when Nb is contained in the range of 0.1% to 30% in aluminum oxide, there is an effect of reducing the crystal grain size. By controlling the surface roughness of the aluminum oxide film surface to a small state, adhesion of the workpiece can be reduced. Furthermore, the wear characteristics can be improved. By miniaturizing the crystal grain size of aluminum oxide, the surface was smoothed, and the adhesion, affinity and fracture resistance with the workpiece were improved. On the other hand, if Nb is less than 0.1%, the effect of refining the crystal grain size cannot be obtained. On the other hand, if it exceeds 30%, the wear resistance of the aluminum oxide film is inferior, which is inconvenient. The coating of the present invention is preferably physical vapor deposition (hereinafter referred to as PVD). This is because compressive residual stress can be applied to the film. Preferable PVD includes sputtering and arc discharge ion plating (hereinafter referred to as AIP). When adding various elements, PVD can be easily added to the aluminum oxide film by preparing a metal target material containing Nb as an additive element in advance. That is, the element addition is possible by simultaneously operating the vapor deposition source 1 equipped with the aluminum oxide target and the vapor deposition source 2 equipped with the metal target containing the additive element in the vacuum apparatus. Examples of the crystal structure of the aluminum oxide film include α-type, γ-type, κ-type, and amorphous phase. The effect of the present invention can also be obtained in any of these cases or when they are mixed. A preferred crystal structure is α-type aluminum oxide.

本願発明の被覆部材の最表層は、Nbの1部をTi、Cr、Si、B、から選択される1種以上で置換することによって、硬質皮膜の凝着性、耐摩耗性について一層の改善効果を有する。置換量はは原子%で、0.1%から30%の範囲であることが好ましい。この理由は、Ti、Cr、Si、Bの置換が酸化アルミニウムの結晶粒径の微細化に効果を有するためであると考えられる。更に、Ti、Si元素は皮膜の高硬度化に効果的である。また、Cr、Bは凝着性の改善に効果的である。上記以外に、W、V元素の添加によっても結晶粒径の微細化に効果を有すると考えられる。一方、置換量が0.1%未満では、上記の効果を得ることができない。また、30%を超えると酸化アルミニウム皮膜の耐摩耗性が劣るため、不都合である。
最表層とは異なる別の少なくとも1層が、金属成分として、Ti、Al、Cr、Si、Nbから選択される2種以上を含有する窒化物、ホウ化物、炭化物及び酸化物の何れか又はそれらの固溶体又は混合物のから構成されることによって、被覆部材の基材と皮膜との密着性を確保し、耐摩耗性を改善するために有効であり好ましい。これらの硬質皮膜は、酸化アルミニウム皮膜の下層に用い、酸化アルミニウム皮膜との密着強度に優れ、酸化アルミニウム皮膜の結晶粒子を微細化することができるため、好ましい層構造である。硬質皮膜は、例えば、(AlTi)N、(TiSi)N、(AlSi)N、(AlTiSi)N、(AlCr)N、(AlCrSi)N、(TiSiB)N等が挙げられる。これらは酸化アルミニウム皮膜との密着強度に優れ、酸化アルミニウム層の結晶粒子を微細化することにとって好適である。
最表層のRa値、Ry値を、Ra≦0.03μm、Ry≦0.5μm、とすることが好ましい。この範囲に制御することによって、酸化アルミニウム皮膜表面の結晶粒子の凹凸が小さく、摩耗環境下において、被加工物の結晶粒子への付着を最小限に抑えることが可能となる。また剥離や結晶粒子の脱落を回避し、最表層に酸化アルミニウム皮膜を有する効果が十分に発揮される。一方、酸化アルミニウム層の面粗度が、Ra>0.03μm、Ry>0.5μmの範囲では、摩耗環境下において、酸化アルミニウム皮膜を被覆する効果が得られない。この理由は、摩耗環境下において、酸化アルミニウム皮膜表面の結晶粒子の凹凸により、被加工物が結晶粒子に付着し、剥離や結晶粒子の脱落を誘発させるためである。そこで本願発明は、酸化アルミニウム皮膜表面を、Ra≦0.03μm、Ry≦0.5μm、にすることが好ましい。Ra値、Ry値の測定方法は、JIS規格に準ずる。測定装置は、接触式の面粗度測定器、非接触の三次元粗さ測定器、原子間力顕微鏡等により測定することができる。本願発明の面粗さを測定する部位は、摩耗環境下において被加工物と接触する部位が好ましい。例えば切削工具では、刃先の逃げ面が好ましい。
最表層の面粗さを、本願発明の好ましい値にするための手段として、酸化アルミニウム皮膜を被覆後、機械的処理することが好ましい。機械的処理としては、研削加工、研摩加工が挙げられる。特にダイヤモンド粒子を含有した投射材による鏡面加工が好適である。被覆後に機械的処理を行うことにより、酸化アルミニウム皮膜内に炭素、酸素等の非金属元素がナノメートルオーダーで含有され、耐摩耗性を改善する。特に、酸化アルミニウム表層から膜厚方向に100nm以内の深さ領域で酸素及び/又は炭素濃度が最大となる場合、硬質皮膜表面への被加工物の凝着抑制に有効である。
The outermost layer of the covering member of the present invention is a further improvement in the adhesion and wear resistance of the hard coating by replacing one part of Nb with one or more selected from Ti, Cr, Si, B. Has an effect. The amount of substitution is atomic%, preferably in the range of 0.1% to 30%. The reason for this is considered that the substitution of Ti, Cr, Si, and B has an effect on the refinement of the crystal grain size of aluminum oxide. Furthermore, Ti and Si elements are effective in increasing the hardness of the film. Cr and B are effective in improving adhesion. In addition to the above, it is considered that the addition of W and V elements has an effect on the refinement of the crystal grain size. On the other hand, if the substitution amount is less than 0.1%, the above effect cannot be obtained. On the other hand, if it exceeds 30%, the wear resistance of the aluminum oxide film is inferior, which is inconvenient.
At least one layer different from the outermost layer is any one of nitride, boride, carbide and oxide containing two or more selected from Ti, Al, Cr, Si, and Nb as a metal component, or those It is effective and preferable in order to ensure the adhesiveness of the base material of a coating | coated member and a membrane | film | coat, and to improve abrasion resistance. These hard coatings are a preferred layer structure because they are used in the lower layer of the aluminum oxide coating, have excellent adhesion strength with the aluminum oxide coating, and can make the crystal grains of the aluminum oxide coating finer. Examples of the hard coating include (AlTi) N, (TiSi) N, (AlSi) N, (AlTiSi) N, (AlCr) N, (AlCrSi) N, and (TiSiB) N. These are excellent in adhesion strength with an aluminum oxide film, and are suitable for making crystal grains of an aluminum oxide layer fine.
The Ra value and Ry value of the outermost layer are preferably Ra ≦ 0.03 μm and Ry ≦ 0.5 μm. By controlling within this range, the unevenness of the crystal particles on the surface of the aluminum oxide film is small, and adhesion of the workpiece to the crystal particles can be minimized in a wear environment. In addition, the effect of having an aluminum oxide film on the outermost layer is sufficiently exhibited while avoiding peeling and falling off of crystal grains. On the other hand, when the surface roughness of the aluminum oxide layer is in the range of Ra> 0.03 μm and Ry> 0.5 μm, the effect of covering the aluminum oxide film cannot be obtained in a wear environment. The reason for this is that the workpiece adheres to the crystal particles due to the unevenness of the crystal particles on the surface of the aluminum oxide film in a wear environment, and induces peeling or dropping of the crystal particles. Therefore, in the present invention, the surface of the aluminum oxide film is preferably set to Ra ≦ 0.03 μm and Ry ≦ 0.5 μm. The measuring method of Ra value and Ry value is based on JIS standard. The measuring device can be measured by a contact-type surface roughness measuring device, a non-contact three-dimensional roughness measuring device, an atomic force microscope, or the like. The site | part which measures the surface roughness of this invention has a preferable site | part which contacts a workpiece in a wear environment. For example, in a cutting tool, the flank of the cutting edge is preferable.
As a means for setting the surface roughness of the outermost layer to a preferable value of the present invention, it is preferable to perform a mechanical treatment after coating the aluminum oxide film. Examples of the mechanical treatment include grinding and polishing. In particular, mirror finishing with a projection material containing diamond particles is suitable. By performing a mechanical treatment after coating, non-metallic elements such as carbon and oxygen are contained in the aluminum oxide film on the nanometer order, thereby improving the wear resistance. In particular, when the oxygen and / or carbon concentration becomes maximum in the depth region within 100 nm in the film thickness direction from the aluminum oxide surface layer, it is effective in suppressing adhesion of the workpiece to the hard coating surface.

本願発明の被覆部材の基材は、WC基超硬合金、サーメット、高速度鋼、セラミックス、立方晶型窒化硼素焼結体及びダイヤモンド焼結体のいずれかから構成される場合、優れた耐摩耗性を発揮するため好ましい。WC基超硬合金は、WCの平均粒度が0.2μm以上、0.6μm未満が好ましく、Co含有量としては、3から8重量%が本発明の効果を達成する上で好ましい。本願発明の被覆部材は、特に切削工具の摩耗抑制に対して有効であり、エンドミル、ドリル、タップ、インサート工具が挙げられる。本願発明を、例えば、切削工具に適用した場合、高速、ドライ加工など、温度が非常に高温、被加工物が凝着し易い環境下において優れた耐摩耗性を示し、長時間加工することができる。また、金型、軸受け、ダイス、ロールなど耐摩耗工具等へ適用した場合も、長寿命化が可能である。以下、実施例に基づいて説明する。   When the base material of the covering member of the present invention is composed of any of WC-based cemented carbide, cermet, high speed steel, ceramics, cubic boron nitride sintered body and diamond sintered body, excellent wear resistance It is preferable because it exhibits its properties. The WC-based cemented carbide preferably has an average particle size of WC of 0.2 μm or more and less than 0.6 μm, and the Co content is preferably 3 to 8% by weight for achieving the effects of the present invention. The covering member of the present invention is particularly effective for suppressing wear of a cutting tool, and examples thereof include an end mill, a drill, a tap, and an insert tool. When the present invention is applied to, for example, a cutting tool, it exhibits excellent wear resistance in an environment where the temperature is very high and the workpiece tends to adhere, such as high speed and dry processing, and can be processed for a long time. it can. Also, when applied to wear-resistant tools such as dies, bearings, dies, and rolls, it is possible to extend the life. Hereinafter, a description will be given based on examples.

本願発明の硬質皮膜等の被覆は、AIP法とアンバランスドマグネトロンスパッタ(以下、UBMSと記す。)法で行った。成膜装置内に複数のAIP蒸発源及びUBMS蒸発源を配置し、蒸発源の前面に回転可能な保持具に超硬合金の基材を装着した。基材は、WC基超硬合金製、WC粒度:0.6〜0.8μm、Co含有量:8重量%、Cr、Taを含有する直径10mmの2枚刃の刃先交換式ボールエンドミルとした。AIP蒸発源に所定の金属ターゲット材をセットし、UBMS蒸発源に酸化アルミニウムをセットした。そして、成膜装置内を真空度5×10−3Pa以下に真空引きした後、基材を500℃まで加熱して1時間保持した。ガス導入口よりArガスを導入して成膜装置内を2Paに保った状態で、基材に−300Vの電圧を印加した。Arガス中でグロー放電を発生させ、Arイオンにより基材表面をクリーニングした。基材に所定のバイアス電圧を印加した後、AIP蒸発源を真空アーク放電させて、ガス導入口より窒素ガス、又は必要に応じ、炭素又は酸素を含むガスを成膜装置内に導入して下層を形成した。ガス導入口よりAr及び酸素ガスを成膜装置内に導入して、別々のUBMS蒸発源からアルミニウム成分と他の金属成分とを同時放電することにより、酸化アルミニウム層にアルミニウム以外の金属元素を添加した。下層は層厚で約3μm被覆し、最表層の酸化アルミニウムとNbを含有する皮膜は約1μm被覆した。下層と最表層の酸化アルミニウム皮膜とが連続的に成長するように、下層の表面を十分に酸化させた後に酸化アルミニウム皮膜を形成した。なお、下層の被覆と酸化アルミニウム層の被覆は、必ずしも同一成膜装置で連続的に行う必要は無い。酸化アルミニウム皮膜の結晶の安定性を考慮すると、下層と酸化アルミニウム皮膜とを別々の成膜装置で処理することが好ましい場合もある。上記の方法によって、本発明例1から17を作成した。本発明例1から17の面粗さRa値、Ry値を接触式の面粗度測定器により測定した。必要に応じて被覆前の基材を鏡面加工し、Ra値が0.01μm以下とした。面粗さの調整には被覆後、機械的な手法により面粗さを調整した。採用した機械的手法は、ダイヤモンドを含有した投射材を硬質皮膜表面に投射した。表1に硬質皮膜組成、面粗さを示す。   The coating of the hard coating of the present invention was performed by the AIP method and the unbalanced magnetron sputtering (hereinafter referred to as UBMS) method. A plurality of AIP evaporation sources and UBMS evaporation sources were arranged in the film forming apparatus, and a cemented carbide base material was mounted on a rotatable holder on the front surface of the evaporation source. The base material was made of a WC-based cemented carbide alloy, WC particle size: 0.6 to 0.8 μm, Co content: 8 wt%, a two-blade 10 mm diameter blade-end replaceable ball end mill containing Cr and Ta. . A predetermined metal target material was set in the AIP evaporation source, and aluminum oxide was set in the UBMS evaporation source. And after evacuating the inside of the film-forming apparatus to 5 * 10 <-3> Pa or less, the base material was heated to 500 degreeC and hold | maintained for 1 hour. A voltage of −300 V was applied to the base material in a state where Ar gas was introduced from the gas inlet and the inside of the film forming apparatus was kept at 2 Pa. Glow discharge was generated in Ar gas, and the substrate surface was cleaned with Ar ions. After applying a predetermined bias voltage to the substrate, the AIP evaporation source is subjected to vacuum arc discharge, and nitrogen gas or, if necessary, gas containing carbon or oxygen is introduced into the film forming apparatus from the gas inlet, and the lower layer Formed. Add metal elements other than aluminum to the aluminum oxide layer by introducing Ar and oxygen gas from the gas inlet into the deposition system and simultaneously discharging the aluminum component and other metal components from separate UBMS evaporation sources did. The lower layer was coated with a thickness of about 3 μm, and the outermost film containing aluminum oxide and Nb was coated with about 1 μm. The aluminum oxide film was formed after sufficiently oxidizing the surface of the lower layer so that the lower layer and the outermost aluminum oxide film grew continuously. Note that the coating of the lower layer and the coating of the aluminum oxide layer are not necessarily performed continuously by the same film forming apparatus. In consideration of the crystal stability of the aluminum oxide film, it may be preferable to treat the lower layer and the aluminum oxide film with separate film forming apparatuses. Invention Examples 1 to 17 were prepared by the above method. The surface roughness Ra and Ry values of Invention Examples 1 to 17 were measured with a contact-type surface roughness measuring device. If necessary, the substrate before coating was mirror-finished so that the Ra value was 0.01 μm or less. To adjust the surface roughness, the surface roughness was adjusted by a mechanical method after coating. The adopted mechanical method was to project a projection material containing diamond onto the surface of the hard coating. Table 1 shows the hard coating composition and surface roughness.

本発明例1から17は、最表層の酸化アルミニウム皮膜を被覆する際に、表1に示す金属成分を添加して、酸化アルミニウム皮膜にアルミニウム以外の金属元素を添加した場合を示す。図1は、機械的処理を施した本発明例1の電子顕微鏡写真を示す。突起状を有した酸化アルミニウムの結晶粒子が明確に確認されなかった。また、凸形状を有した酸化アルミニウムの結晶粒子もほとんど確認されなかった。図2は、機械的処理を行っていない比較例18の電子顕微鏡写真を示す。突起状を有した酸化アルミニウムの結晶粒子が明瞭に確認された。   Invention Examples 1 to 17 show cases where the metal component shown in Table 1 was added and a metal element other than aluminum was added to the aluminum oxide film when the outermost aluminum oxide film was coated. FIG. 1 shows an electron micrograph of Example 1 of the present invention subjected to mechanical treatment. Protrusion-like aluminum oxide crystal particles were not clearly observed. Further, almost no aluminum oxide crystal particles having a convex shape were observed. FIG. 2 shows an electron micrograph of Comparative Example 18 in which no mechanical treatment was performed. Crystal grains of aluminum oxide having protrusions were clearly confirmed.

硬質皮膜を評価するために、切削工具に関して耐摩耗性の評価を行った。下記切削条件によって被加工物との凝着性、親和性、耐欠損性及び耐摩耗性の評価を実施した。寿命判定は、最大摩耗幅が0.1mmに達するまでの切削長とした。但し、10m未満を切り捨てて表1に併記した。
(切削条件)
加工方法:ドライ加工、底面直線加工、ダウンカット加工
被加工物:FCD450
切削速度:160m/分
一刃当たりの送り量:0.3mm/刃
切り込み深さ:軸方向0.25mm、ピックフィード0.5mm
本発明例は、比較例に比べ耐摩耗性に優れ、本願発明の効果が確認された。図3に、本発明例1、比較例18、20の耐摩耗性評価結果を示す。本発明例1は、酸化アルミニウム皮膜の剥離が無く、大幅な摩耗特性の改善が認められた。本発明例1から3より、面粗さの相違による耐摩耗性を比較した。Nb元素の添加に加え、Nbの1部を他の元素で置換した方が、Ra値、Ry値はより小さい値となり、耐摩耗性に優れる結果となった。本発明例1、本発明例4から6は、酸化アルミニウム皮膜の結晶構造が異なる場合を示す。何れの結晶構造においても優れた耐摩耗性を示した。本発明例7は、下層に(AlCr)Nを有する場合を示す。本発明例8は、(AlCrSi)N、本発明例9は、(AlTiSiN)、本発明例10は、(AlTi)Nと(SiTi)Nを被覆しその後、酸化アルミニウム皮膜を被覆した場合、本発明例11は、(AlTi)Nと(AlCrSi)Nを被覆しその後、酸化アルミニウム皮膜を被覆した場合を示す。何れの場合も、耐摩耗性の改善効果が確認された。本発明例12は、下層が(AlZr)Nの場合を示すが、下層にはTi、Al、Cr、Si、Nbから選択される2種以上を含有する皮膜がより好まし結果となった。本発明例13は、下層が(AlTiNb)Nを有する場合、本発明例14は(AlTi)Nを有する場合、本発明例15から本発明例17は、酸化アルミニウム皮膜にNbCr、NbV、NbTiBの各元素を添加した場合を示し、何れも耐摩耗性に優れていた。
In order to evaluate the hard coating, the wear resistance of the cutting tool was evaluated. Evaluation of adhesion, affinity, fracture resistance, and wear resistance with the workpiece was performed under the following cutting conditions. The life judgment was the cutting length until the maximum wear width reached 0.1 mm. However, less than 10 m was rounded down and shown in Table 1.
(Cutting conditions)
Processing method: Dry processing, bottom straight processing, down cut processing Workpiece: FCD450
Cutting speed: 160 m / min Feed amount per blade: 0.3 mm / blade Cutting depth: 0.25 mm in the axial direction, pick feed 0.5 mm
The inventive examples were superior in wear resistance compared to the comparative examples, and the effects of the present invention were confirmed. In FIG. 3, the abrasion resistance evaluation result of this invention example 1 and the comparative examples 18 and 20 is shown. In Invention Example 1, there was no peeling of the aluminum oxide film, and a significant improvement in wear characteristics was observed. From Inventive Examples 1 to 3, the wear resistance due to the difference in surface roughness was compared. In addition to the addition of the Nb element, the substitution of one part of Nb with another element resulted in smaller Ra and Ry values, which resulted in excellent wear resistance. Invention Example 1 and Invention Examples 4 to 6 show cases where the crystal structures of the aluminum oxide films are different. In any crystal structure, excellent wear resistance was exhibited. Invention Example 7 shows a case where (AlCr) N is present in the lower layer. Invention Example 8 is (AlCrSi) N, Invention Example 9 is (AlTiSiN), Invention Example 10 is coated with (AlTi) N and (SiTi) N, and then coated with an aluminum oxide film. Invention Example 11 shows a case where (AlTi) N and (AlCrSi) N are coated and then an aluminum oxide film is coated. In any case, the effect of improving the wear resistance was confirmed. Invention Example 12 shows a case in which the lower layer is (AlZr) N, but a film containing two or more selected from Ti, Al, Cr, Si, and Nb was more preferable in the lower layer. Inventive Example 13 includes (AlTiNb) N in the lower layer, Inventive Example 14 includes (AlTi) N, and Inventive Examples 15 to 17 are formed of NbCr, NbV, NbTiB on the aluminum oxide film. The case where each element was added was shown, and all were excellent in abrasion resistance.

図4に比較例18の切削初期における刃先近傍の電子顕微鏡写真を示す。比較例18は切削初期に酸化アルミニウム層の剥離が認められた。この理由は、切削開始直後に突起状を有した酸化アルミニウムの結晶粒子に多数の被加工物から構成される凝着物の付着があったために、これら凝着物の成長に伴って剥離が発生したためである。従って、最表層の酸化アルミニウム皮膜は多数の凝着物を有し、下層から大きく剥離が発生して、酸化アルミニウム層が機能しなかった。比較例18、19は、比較例20の酸化アルミニウム層が表面にない場合と同様に、耐摩耗性の改善が認められなかった。   FIG. 4 shows an electron micrograph of the vicinity of the cutting edge of Comparative Example 18 in the initial stage of cutting. In Comparative Example 18, peeling of the aluminum oxide layer was observed at the beginning of cutting. The reason for this is that, since there was adhesion of a large number of workpieces to the aluminum oxide crystal particles with protrusions immediately after the start of cutting, peeling occurred with the growth of these adhesions. is there. Therefore, the aluminum oxide film on the outermost layer had a large number of adherents, a large amount of peeling occurred from the lower layer, and the aluminum oxide layer did not function. In Comparative Examples 18 and 19, as in the case where the aluminum oxide layer of Comparative Example 20 was not on the surface, no improvement in wear resistance was observed.

図1は、本発明例1の表面電子顕微鏡写真を示す。FIG. 1 shows a surface electron micrograph of Example 1 of the present invention. 図2は、比較例18の表面電子顕微鏡写真を示す。FIG. 2 shows a surface electron micrograph of Comparative Example 18. 図3は、摩耗曲線を示す。FIG. 3 shows the wear curve. 図4は、比較例18の刃先近傍の電子顕微鏡写真を示す。FIG. 4 shows an electron micrograph of the vicinity of the cutting edge of Comparative Example 18.

Claims (5)

硬質皮膜を被覆した被覆部材において、該被覆部材は物理蒸着を用いて成膜された最表層を有し、該最表層は酸化アルミニウムとNbを含有することを特徴とする被覆部材。 A covering member coated with a hard film, wherein the covering member has an outermost layer formed by physical vapor deposition, and the outermost layer contains aluminum oxide and Nb. 請求項1記載の被覆部材において、該最表層は、Nbの1部をTi、Cr、Si、B、から選択される1種以上で置換したことを特徴とする被覆部材。 2. The covering member according to claim 1, wherein the outermost layer is formed by replacing one part of Nb with one or more selected from Ti, Cr, Si, and B. 3. 請求項1又は2記載の被覆部材において、該被覆部材は、最表層とは別の層が、金属成分として、Ti、Al、Cr、Si、Nbから選択される2種以上を含有する窒化物、硼化物、炭化物及び酸化物の何れか又はそれらの固溶体又は混合物からなる硬質皮膜を具えることを特徴とする被覆部材。 The covering member according to claim 1 or 2, wherein the covering member includes a layer different from the outermost layer, and contains two or more kinds selected from Ti, Al, Cr, Si, and Nb as metal components. A covering member comprising a hard film made of any one of boride, carbide and oxide, or a solid solution or a mixture thereof. 請求項1乃至3いずれかに記載の被覆部材において、該最表層の面粗さRa、Ryが(μm)で、Ra≦0.03、Ry≦0.5、であることを特徴とする被覆部材。 The covering member according to any one of claims 1 to 3, wherein the surface roughness Ra, Ry of the outermost layer is (µm), and Ra ≤ 0.03, Ry ≤ 0.5. Element. 請求項1乃至4いずれかに記載の被覆部材において、該最表層を機械的処理により平滑にしたことを特徴とする被覆部材。
5. The covering member according to claim 1, wherein the outermost layer is smoothed by a mechanical treatment.
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Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2010115704A (en) * 2008-10-15 2010-05-27 Hitachi Metals Ltd Coated metallic mold for plastic processing
JP2010201576A (en) * 2009-03-04 2010-09-16 Mitsubishi Materials Corp Surface coated cutting tool with hard coating layer exerting excellent chipping resistance and wear resistance
JP2010284710A (en) * 2009-06-15 2010-12-24 Hitachi Metals Ltd Coated mold for plastic working, and method for manufacturing the same
WO2014119212A1 (en) * 2013-01-29 2014-08-07 株式会社神戸製鋼所 Hard coating film having adhesion resistance to soft metal
JP2018030215A (en) * 2016-08-26 2018-03-01 三菱マテリアル株式会社 Surface coated cutting tool with excellent chipping resistance and wear resistance with hard coating layer

Cited By (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2010115704A (en) * 2008-10-15 2010-05-27 Hitachi Metals Ltd Coated metallic mold for plastic processing
JP2010201576A (en) * 2009-03-04 2010-09-16 Mitsubishi Materials Corp Surface coated cutting tool with hard coating layer exerting excellent chipping resistance and wear resistance
JP2010284710A (en) * 2009-06-15 2010-12-24 Hitachi Metals Ltd Coated mold for plastic working, and method for manufacturing the same
WO2014119212A1 (en) * 2013-01-29 2014-08-07 株式会社神戸製鋼所 Hard coating film having adhesion resistance to soft metal
JP2014145114A (en) * 2013-01-29 2014-08-14 Kobe Steel Ltd Hard film excellent in adhesion resistance to soft metal
CN104937130A (en) * 2013-01-29 2015-09-23 株式会社神户制钢所 Hard coating film having adhesion resistance to soft metal
US9410235B2 (en) 2013-01-29 2016-08-09 Kobe Steel, Ltd. Hard coating film having anti-adhesion property to soft metal
CN104937130B (en) * 2013-01-29 2017-07-28 株式会社神户制钢所 Hard film with adhesion resistance to soft metals
JP2018030215A (en) * 2016-08-26 2018-03-01 三菱マテリアル株式会社 Surface coated cutting tool with excellent chipping resistance and wear resistance with hard coating layer

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