JP2008093754A - Surface coated cutting tool with hard coated layer exhibiting excellent chipping resistance - Google Patents

Surface coated cutting tool with hard coated layer exhibiting excellent chipping resistance Download PDF

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JP2008093754A
JP2008093754A JP2006275697A JP2006275697A JP2008093754A JP 2008093754 A JP2008093754 A JP 2008093754A JP 2006275697 A JP2006275697 A JP 2006275697A JP 2006275697 A JP2006275697 A JP 2006275697A JP 2008093754 A JP2008093754 A JP 2008093754A
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titanium
chromium
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cutting tool
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Tetsuhiko Honma
哲彦 本間
Keiji Nakamura
惠滋 中村
Hisashi Honma
尚志 本間
Akira Osada
晃 長田
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Mitsubishi Materials Corp
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Abstract

<P>PROBLEM TO BE SOLVED: To provide a surface coated cutting tool with a hard coated layer exhibiting excellent chipping resistance in high speed heavy cutting machining. <P>SOLUTION: A lower part layer is constituted of (a) a titanium carbonitride layer, (b) a Ti-Cr composite carbonitride layer an inclusion ratio of chrome of which is 0.01-0.1 (atomic ratio) and a Ti system compound laminated layer constituted by alternately laminating the above (a), (b), an upper layer is constituted of (c) a composite oxide layer of aluminum and chrome an inclusion ratio of chrome of which is 0.01-0.1 (atomic ratio) and additionally, the Ti-Cr composite carbonitride layer of the above (b) is constituted of the Ti-Cr composite carbonitride layer in which the highest peak exists in Σ3 in a constitutive atom covalent lattice point distribution graph formed in accordance with a measuring result of an inclination made by a normal of a (001) face and a (011) face of a crystal grain existing in a measuring area of a surface polishing face and a normal of the surface polishing face and a distribution ratio of Σ3 occupying in the whole of ΣN+1 is more than 60%. <P>COPYRIGHT: (C)2008,JPO&INPIT

Description

この発明は、特に鋼、ステンレス鋼および鋳鉄などのミーリング加工を、高速で、かつ、高送り、高切り込みなどの高速重切削条件で行った場合に、硬質被覆層がすぐれた耐チッピング性を発揮する表面被覆切削工具(以下、被覆工具という)に関するものである。   This invention exhibits excellent chipping resistance with a hard coating layer, especially when milling of steel, stainless steel, cast iron, etc. is performed at high speed and under high speed heavy cutting conditions such as high feed and high cutting. The present invention relates to a surface-coated cutting tool (hereinafter referred to as a coated tool).

従来、一般に、炭化タングステン(以下、WCで示す)基超硬合金または炭窒化チタン(以下、TiCNで示す)基サーメットで構成された基体(以下、これらを総称して工具基体という)の表面に、
(a)下部層が、Tiの炭化物(以下、TiCで示す)層、窒化物(以下、同じくTiNで示す)層、炭窒化物(以下、TiCNで示す)層、炭酸化物(以下、TiCOで示す)層、および炭窒酸化物(以下、TiCNOで示す)層のうちの1層または2層以上からなり、かつ3〜20μmの全体平均層厚を有するTi化合物層、
(b)上部層が、1〜15μmの平均層厚、および化学蒸着した状態でα型の結晶構造を有し、さらに、
組成式:(Al1−QCr、(ただし、原子比で、Q:0.01〜0.1)、
を満足するAlとCrの複合酸化物[以下、(Al,Cr)23で示す)]層、
以上(a)および(b)で構成された硬質被覆層を蒸着形成してなる被覆工具が知られており、この被覆工具が、例えば各種の鋼や鋳鉄などの連続切削や断続切削に用いられることも良く知られるところである。
Conventionally, generally on the surface of a substrate (hereinafter collectively referred to as a tool substrate) composed of a tungsten carbide (hereinafter referred to as WC) -based cemented carbide or titanium carbonitride (hereinafter referred to as TiCN) -based cermet. ,
(A) The lower layer is a Ti carbide (hereinafter referred to as TiC) layer, a nitride (hereinafter also referred to as TiN) layer, a carbonitride (hereinafter referred to as TiCN) layer, a carbon oxide (hereinafter referred to as TiCO). A Ti compound layer consisting of one or two or more layers of carbonitride oxide (hereinafter referred to as TiCNO) layers and having an overall average layer thickness of 3 to 20 μm,
(B) the upper layer has an average layer thickness of 1 to 15 μm and an α-type crystal structure in the state of chemical vapor deposition;
Composition formula: (Al 1 -Q Cr Q ) 2 O 3 (however, in terms of atomic ratio, Q: 0.01 to 0.1),
A composite oxide of Al and Cr satisfying the following conditions (hereinafter referred to as (Al, Cr) 2 O 3 )] layer
A coated tool formed by vapor-depositing the hard coating layer constituted by (a) and (b) above is known, and this coated tool is used for continuous cutting and intermittent cutting of various steels and cast irons, for example. This is also well known.

また、上記の被覆工具において、これの硬質被覆層の構成層は、一般に粒状結晶組織を有し、さらに、下部層であるTi化合物層を構成するTiCN層を、層自身の強度向上を目的として、通常の化学蒸着装置にて、反応ガスとして有機炭窒化物を含む混合ガスを使用し、700〜950℃の中温温度域で化学蒸着することにより形成して縦長成長結晶組織をもつようにすることも知られている。
特開昭52−66508号公報 特開平6−8010号公報
Further, in the above-mentioned coated tool, the constituent layer of the hard coating layer generally has a granular crystal structure, and the TiCN layer constituting the Ti compound layer as the lower layer is used for the purpose of improving the strength of the layer itself. In a normal chemical vapor deposition apparatus, a gas mixture containing organic carbonitride is used as a reaction gas, and it is formed by chemical vapor deposition at an intermediate temperature range of 700 to 950 ° C. so as to have a vertically grown crystal structure. It is also known.
JP 52-66508 A Japanese Patent Laid-Open No. 6-8010

近年の切削装置の高性能化はめざましく、一方で切削加工の省力化および省エネ化に対する要求は強く、これに伴い、切削加工は一段と高速化、また、高送り高切込み化の傾向にあるが、上記の従来被覆工具においては、これを鋼、ステンレス鋼および鋳鉄などの通常の加工条件でのミーリング切削に用いた場合には問題はないが、これを高速高送り高切込み加工に用いた場合、硬質被覆層のTiCN層の高温強度が十分でないために、高速高送り高切り込みミーリング加工下における機械的・熱的な負荷に耐えることができず、早期にチッピング(微小欠け)が発生し、比較的短時間で使用寿命に至るのが現状である。   In recent years, the performance of cutting machines has been remarkable. On the other hand, there are strong demands for labor saving and energy saving of cutting work. In the above conventional coated tool, there is no problem when this is used for milling cutting under normal processing conditions such as steel, stainless steel and cast iron, but when this is used for high-speed high-feed high-cutting, Since the high temperature strength of the TiCN layer of the hard coating layer is not sufficient, it cannot withstand mechanical and thermal loads under high-speed, high-feed, high-cut milling processing, and chipping (small chipping) occurs early. At present, the service life is reached in a short time.

そこで、本発明者等は、上述のような観点から、上記のアルミニウムとクロムの複合酸化物層(Al−Cr複合酸化物層)が硬質被覆層の上部層を構成する被覆工具の耐チッピング性向上を図るべく、図1(a)に示される模式図のように、格子点にTi、炭素、および窒素からなる構成原子がそれぞれ存在するNaCl型面心立方晶の結晶構造(なお、図1(b)は(011)面で切断した状態を示す)を有し、かつ所定の高温硬さを示すTiCN層に着目し、研究を行った結果、
(a)従来被覆工具の硬質被覆層を構成するTiCN層は、例えば、通常の化学蒸着装置にて、
反応ガス組成:容量%で、TiCl:2〜10%、CHCN:1〜5%、N2:10〜30%、H2:残り、
反応雰囲気温度:800〜930℃、
反応雰囲気圧力:15〜25kPa、
の条件(通常条件という)で蒸着形成されるが、
これらの通常条件において、上記の反応ガスに、CrClを0.02〜1容量%の割合で添加し、これ以外は同一の条件で層の蒸着形成を行うと、この結果形成されたチタン(Ti)とクロム(Cr)の複合炭窒化物層(以下、「Ti−Cr複合炭窒化物層」で示す)は、CrをTiとの合量に占める割合で1〜10原子%の割合で含有し、上記の従来TiCN層と同じNaCl型面心立方晶の結晶構造(上記図1参照)、すなわち、Ti原子の一部がCr原子で置換されたNaCl型面心立方晶の結晶構造をもつものになると共に、置換含有したCrの作用で、高温強度が一段と向上したものになるため、切刃部にきわめて高い機械的・熱的負荷がかかる高速高送り、高切り込みミーリング切削において、前記硬質被覆層の耐チッピング性向上に寄与すること。
In view of the above, the present inventors have found that the above-described chipping resistance of the coated tool in which the composite oxide layer of aluminum and chromium (Al—Cr composite oxide layer) constitutes the upper layer of the hard coating layer. In order to improve, as shown in the schematic diagram shown in FIG. 1A, a crystal structure of a NaCl type face centered cubic crystal in which constituent atoms consisting of Ti, carbon, and nitrogen are present at lattice points (see FIG. 1). (B) shows a state cut at the (011) plane), and as a result of conducting research by paying attention to a TiCN layer showing a predetermined high-temperature hardness,
(A) The TiCN layer constituting the hard coating layer of the conventional coated tool is, for example, a normal chemical vapor deposition apparatus.
Reaction gas composition: by volume%, TiCl 4: 2~10%, CH 3 CN: 1~5%, N 2: 10~30%, H 2: remainder,
Reaction atmosphere temperature: 800-930 ° C.
Reaction atmosphere pressure: 15-25 kPa,
It is formed by vapor deposition under the conditions (called normal conditions)
Under these normal conditions, when CrCl 3 was added to the above reaction gas at a ratio of 0.02 to 1% by volume, and a layer was formed under the same conditions except for this, titanium (as a result) was formed. Ti) and chromium (Cr) composite carbonitride layer (hereinafter referred to as “Ti-Cr composite carbonitride layer”) is a ratio of 1 to 10 atomic% of Cr in the total amount with Ti. And the same NaCl-type face-centered cubic crystal structure as that of the conventional TiCN layer (see FIG. 1 above), that is, a NaCl-type face-centered cubic crystal structure in which some Ti atoms are replaced by Cr atoms. In addition, the high-temperature strength is further improved by the action of Cr containing substitution, so in the high-speed high-feed, high-cut milling cutting that requires extremely high mechanical and thermal load on the cutting edge, Chipping resistance of hard coating Contribute to improvement of performance.

(b)上記の従来被覆工具の硬質被覆層を構成するTiCN層(以下、従来TiCN層という)と、上記(a)のTi−Cr複合炭窒化物層について、
電界放出型走査電子顕微鏡を用い、図2(a),(b)に概略説明図で例示される通り、表面研磨面の測定範囲内に存在する結晶粒個々に電子線を照射して、前記表面研磨面の法線に対して、前記結晶粒の結晶面である(001)面および(011)面の法線がなす傾斜角(図2(a)には前記結晶面のうち(001)面の傾斜角が0度、(011)面の傾斜角が45度の場合、同(b)には(001)面の傾斜角が45度、(011)面の傾斜角が0度の場合を示しているが、これらの角度を含めて前記結晶粒個々のすべての傾斜角)を測定し、この場合前記結晶粒は、上記の通り格子点に、従来TiCN層であればTi、炭素、および窒素からなる構成原子が、さらにTi−Cr複合炭窒化物層であれば、Ti、Cr、炭素および窒素からなる構成原子がそれぞれ存在するNaCl型面心立方晶の結晶構造を有し、この結果得られた測定傾斜角に基づいて、相互に隣接する結晶粒の界面で、前記構成原子のそれぞれが前記結晶相互間で1つの構成原子を共有する格子点(構成原子共有格子点)の分布を算出し、前記構成原子共有格子点間に構成原子を共有しない格子点がN個(NはNaCl型面心立方晶の結晶構造上2以上の偶数となる)存在する構成原子共有格子点形態をΣN+1で表し、個々のΣN+1がΣN+1全体(ただし、頻度の関係でNの上限値を28とする)に占める分布割合を示す構成原子共有格子点分布グラフを作成した場合、前記従来TiCN層は、図4に例示される通り、Σ3の分布割合が30%以下の相対的に低い構成原子共有格子点分布グラフを示すのに対して、前記Ti−Cr複合炭窒化物層は、図3に例示される通り、Σ3に最高ピークが存在し、かつ、Σ3の分布割合が60%以上のきわめて高い構成原子共有格子点分布グラフを示し、しかも、前記Ti−Cr複合炭窒化物層のΣ3の分布割合は、層中のCr含有量によって変化し、さらに、層中のCr含有量は、反応ガス中のCrClの配合割合によって調整できること。
(B) About the TiCN layer (henceforth a conventional TiCN layer) which comprises the hard coating layer of said conventional coated tool, and the Ti-Cr compound carbonitride layer of said (a),
Using a field emission scanning electron microscope, as illustrated in the schematic explanatory diagrams in FIGS. 2A and 2B, each crystal grain existing within the measurement range of the surface polished surface is irradiated with an electron beam, The inclination angle formed by the normal lines of the (001) plane and the (011) plane, which are the crystal planes of the crystal grains, with respect to the normal line of the surface polished surface (FIG. 2A shows (001) of the crystal planes. When the tilt angle of the surface is 0 degree and the tilt angle of the (011) plane is 45 degrees, the tilt angle of the (001) plane is 45 degrees and the tilt angle of the (011) plane is 0 degree. In this case, all the tilt angles of the crystal grains including these angles are measured. In this case, the crystal grains are at lattice points as described above, and Ti, carbon, And if the constituent atoms consisting of nitrogen and Ti-Cr composite carbonitride layer are further Ti, Cr, carbon and nitrogen Each of the constituent atoms has the crystal structure at the interface between crystal grains adjacent to each other based on the measurement tilt angle obtained as a result. The distribution of lattice points (constituent atom shared lattice points) that share one constituent atom between each other is calculated, and N lattice points that do not share constituent atoms between the constituent atom shared lattice points (N is a NaCl type face center) The form of constituent atomic shared lattice points existing in the cubic crystal structure is represented by ΣN + 1, and each ΣN + 1 occupies the entire ΣN + 1 (however, the upper limit value of N is 28 due to frequency) When a constituent atomic shared lattice point distribution graph showing a distribution ratio is created, the conventional TiCN layer has a relatively low constituent atomic shared lattice point distribution graph with a Σ3 distribution ratio of 30% or less as illustrated in FIG. To show In the Ti—Cr composite carbonitride layer, as shown in FIG. 3, the highest peak exists in Σ3, and the distribution ratio of Σ3 is extremely high with a distribution ratio of Σ3 of 60% or more. In addition, the distribution ratio of Σ3 of the Ti—Cr composite carbonitride layer varies depending on the Cr content in the layer, and the Cr content in the layer is the blending ratio of CrCl 3 in the reaction gas. Can be adjusted by.

(c)上記のTi−Cr複合窒化物層の形成に際して、層中のCr含有割合を、Tiとの合量に占める割合で1〜10原子%とすることによって、構成原子共有格子点分布グラフでのΣ3の分布割合が60%以上のきわめて高いものになり、この結果、Ti−Cr複合炭窒化物層は上記従来TiCN層と比べ、一段と高温強度が向上したものとなるのであり、したがって、層中のCr含有割合が前記の範囲から低い方に外れても、あるいは高い方に外れても、構成原子共有格子点分布グラフでのΣ3の分布割合が60%未満になってしまい、所望の高温強度向上効果が得られなくなること。 (C) When forming the Ti—Cr composite nitride layer, the constituent atomic shared lattice point distribution graph is obtained by setting the Cr content ratio in the layer to 1 to 10 atomic% in the ratio to the total amount with Ti. As a result, the Ti—Cr composite carbonitride layer has a further improved high-temperature strength as compared with the conventional TiCN layer. Even if the Cr content ratio in the layer deviates from the above range to the lower side or to the higher side, the distribution ratio of Σ3 in the constituent atom shared lattice point distribution graph becomes less than 60%, and the desired content The effect of improving high-temperature strength cannot be obtained.

(d)上記のTi−Cr複合炭窒化物層は、従来TiCN層が具備する高温硬さと高温強度に加えて、上記従来TiCN層に比べて一段と高い高温強度を有するので、前記Ti−Cr複合炭窒化物層とTiCN層とを積層して蒸着形成してなる被覆工具は、極めて高い機械的・熱的負荷のかかる高速高送り高切り込みミーリング加工においても、前記硬質被覆層がすぐれた耐チッピング性を示し、長期に亘ってすぐれた性能を発揮するようになること。
以上(a)〜(d)に示される研究結果を得たのである。
(D) The Ti—Cr composite carbonitride layer has a higher high-temperature strength than the conventional TiCN layer in addition to the high-temperature hardness and high-temperature strength of the conventional TiCN layer. The coated tool formed by laminating and depositing a carbonitride layer and a TiCN layer is a chipping-resistant chipping that has an excellent hard coating layer even in high-speed, high-feed, high-cut milling processes that require extremely high mechanical and thermal loads. To show the performance and to show the excellent performance for a long time.
The research results shown in (a) to (d) above were obtained.

この発明は、上記の研究結果に基づいてなされたものであって、
「(1) 炭化タングステン基超硬合金または炭窒化チタン基サーメットで構成された工具基体の表面に、下部層と上部層からなる硬質被覆層を蒸着形成した表面被覆切削工具において、
上記下部層は、
(a)1〜5μmの平均層厚を有する炭窒化チタン層、
(b)1〜5μmの平均層厚を有し、かつ、チタンとクロムの合量に対するクロムの含有割合(Cr/(Ti+Cr))が、原子比で0.01〜0.1であるチタンとクロムの複合炭窒化物層、
上記(a)および(b)を少なくとも3層以上交互に積層し、合計平均層厚が5〜15μmとなるよう化学蒸着したチタン系化合物積層、
上記上部層は、
(c)0.5〜5μmの平均層厚を有し、かつ、アルミニウムとクロムの合量に対するクロムの含有割合(Cr/(Al+Cr))が、原子比で0.01〜0.1であるアルミニウムとクロムの複合酸化物層、
からなる硬質被覆層を設けたことを特徴とする硬質被覆層がすぐれた耐チッピング性を発揮する表面被覆切削工具。
(2)前記(1)記載の表面被覆切削工具において、
上記チタン系化合物積層からなる下部層と、上記アルミニウムとクロムの複合酸化物層からなる上部層との間に、炭酸化チタン層、窒酸化チタン層および炭窒酸化チタン層のうちの1種または2種以上からなる合計平均層厚0.2〜1μmの中間層を介在させたことを特徴とする前記(1)記載の表面被覆切削工具。
(3)前記(1)乃至(2)記載の表面被覆切削工具において、
上記(b)のチタンとクロムの複合炭窒化物層は、電界放出型走査電子顕微鏡を用い、表面研磨面の測定範囲内に存在する結晶粒個々に電子線を照射して、前記表面研磨面の法線に対して、前記結晶粒の結晶面である(001)面および(011)面の法線がなす傾斜角を測定し、この場合前記結晶粒は、格子点にチタンとクロムと炭素と窒素からなる構成原子がそれぞれ存在するNaCl型面心立方晶の結晶構造を有し、この結果得られた測定傾斜角に基づいて、相互に隣接する結晶粒の界面で、前記構成原子のそれぞれが前記結晶粒相互間で1つの構成原子を共有する格子点(構成原子共有格子点)の分布を算出し、前記構成原子共有格子点間に構成原子を共有しない格子点がN個(NはNaCl型面心立方晶の結晶構造上2以上の偶数となる)存在する構成原子共有格子点形態をΣN+1で表した場合、個々のΣN+1がΣN+1全体(ただし、頻度の関係で上限値を28とする)に占める分布割合を示す構成原子共有格子点分布グラフにおいて、いずれもΣ3に最高ピークが存在し、かつ前記Σ3のΣN+1全体に占める分布割合が60%以上である構成原子共有格子点分布グラフを示すチタンとクロムの複合炭窒化物層であることを特徴とする前記(1)乃至(2)のいずれかに記載の表面被覆切削工具(被覆工具)。」
に特徴を有するものである。
This invention was made based on the above research results,
“(1) In a surface-coated cutting tool in which a hard coating layer composed of a lower layer and an upper layer is vapor-deposited on the surface of a tool base made of tungsten carbide-based cemented carbide or titanium carbonitride-based cermet,
The lower layer is
(A) a titanium carbonitride layer having an average layer thickness of 1 to 5 μm,
(B) Titanium having an average layer thickness of 1 to 5 μm and a chromium content ratio (Cr / (Ti + Cr)) of 0.01 to 0.1 in terms of atomic ratio relative to the total amount of titanium and chromium Chromium composite carbonitride layer,
(A) and (b) at least three or more layers are alternately stacked, and a titanium-based compound layer is formed by chemical vapor deposition so that the total average layer thickness is 5 to 15 μm.
The upper layer is
(C) It has an average layer thickness of 0.5 to 5 μm, and the content ratio of chromium to the total amount of aluminum and chromium (Cr / (Al + Cr)) is 0.01 to 0.1 in atomic ratio. A complex oxide layer of aluminum and chromium,
A surface-coated cutting tool that exhibits excellent chipping resistance, wherein the hard coating layer is provided with a hard coating layer.
(2) In the surface-coated cutting tool according to (1),
One of a titanium carbonate layer, a titanium nitride oxide layer, and a titanium carbonitride oxide layer between the lower layer made of the titanium-based compound laminate and the upper layer made of the composite oxide layer of aluminum and chromium, or The surface-coated cutting tool according to (1) above, wherein an intermediate layer having a total average layer thickness of 0.2 to 1 μm composed of two or more kinds is interposed.
(3) In the surface-coated cutting tool according to the above (1) to (2),
The composite carbonitride layer of titanium and chromium of (b) is irradiated with an electron beam on each crystal grain existing within the measurement range of the surface polishing surface using a field emission scanning electron microscope, and the surface polishing surface The tilt angle formed by the normal lines of the (001) plane and (011) plane, which are crystal planes of the crystal grains, is measured. In this case, the crystal grains have titanium, chromium, and carbon at lattice points. Each of the constituent atoms has a crystal structure of NaCl type face centered cubic crystal in which constituent atoms composed of nitrogen and nitrogen are present, respectively, at the interface between adjacent crystal grains based on the measured tilt angle. Calculates the distribution of lattice points that share one constituent atom between the crystal grains (constituent atom shared lattice points), and N lattice points that do not share constituent atoms between the constituent atom shared lattice points (N is N An even number of 2 or more in the crystal structure of the NaCl type face centered cubic crystal When the configuration of existing constituent atomic shared lattice points is expressed by ΣN + 1, the constituent atomic shared lattice point distribution graph showing the distribution ratio of each ΣN + 1 to the entire ΣN + 1 (however, the upper limit is 28 due to the frequency) And Σ3 has a highest peak, and the distribution ratio of the Σ3 to the entire ΣN + 1 is 60% or more. The surface-coated cutting tool (coated tool) according to any one of (1) to (2), which is characterized in that "
It has the characteristics.

つぎに、この発明の被覆工具の硬質被覆層の構成層について、上記の通りに限定した理由を説明する。
(a)炭窒化チタン(TiCN)層
TiCN層は、それ自体で所定の高温硬さを有し、切削加工時の摩耗に対して耐摩耗性を示すが、その平均層厚が1μm未満では、十分な耐摩耗性を発揮することができず、また、その平均層厚が5μm以上の場合は、隣接するTi−Cr複合炭窒化物層との十分な付着強度を確保することができずチッピング発生の原因となるため、その平均層厚を1〜5μmとした。
なお、TiCN層としては、例えば、特開平6−8010号公報、特開平7−328808号公報に示されるように、層の高温強度向上を目的として、通常の化学蒸着装置にて、反応ガスとして有機炭窒化物を含む混合ガスを使用して、700〜950℃の中温度領域で化学蒸着することにより形成した縦長成長結晶組織を有するTiCN層(以下、「l−TiCN層」で示す)も知られているが、この発明でいうTiCN層には、上記l−TiCN層も当然に含まれる。
Next, the reason why the constituent layers of the hard coating layer of the coated tool of the present invention are limited as described above will be described.
(A) Titanium carbonitride (TiCN) layer The TiCN layer itself has a predetermined high-temperature hardness and exhibits wear resistance against wear during cutting, but if its average layer thickness is less than 1 μm, If sufficient wear resistance cannot be exhibited and the average layer thickness is 5 μm or more, sufficient adhesion strength with the adjacent Ti—Cr composite carbonitride layer cannot be ensured and chipping is performed. In order to cause generation, the average layer thickness is set to 1 to 5 μm.
As the TiCN layer, as shown in, for example, JP-A-6-8010 and JP-A-7-328808, as a reactive gas in a normal chemical vapor deposition apparatus for the purpose of improving the high-temperature strength of the layer. A TiCN layer having a vertically grown crystal structure (hereinafter referred to as “1-TiCN layer”) formed by chemical vapor deposition in a middle temperature region of 700 to 950 ° C. using a mixed gas containing organic carbonitrides. Although known, the TiCN layer referred to in the present invention naturally includes the 1-TiCN layer.

(b)Ti−Cr複合炭窒化物層
Ti−Cr複合炭窒化物層は、すぐれた高温硬さおよびすぐれた高温強度を有するが、この特性は、反応ガスにCrClを0.02〜1容量%の割合で添加して化学蒸着し、蒸着形成された層中のCr含有割合をTiとの合量に占める割合で1〜10原子%とした結果として、構成原子共有格子点分布グラフにおけるΣ3の分布割合が60%以上となることにより得られるものであって、一方、Σ3の分布割合が60%未満では、高温強度の向上効果が少なく、高速高送り高切り込みミーリング加工において、硬質被覆層にチッピングが発生することは避けられず、すぐれた耐摩耗性を発揮することはできないことから、TiとCrの合量に対するCrの含有割合(Cr/(Ti+Cr))を0.01〜0.1(但し,原子比)と定め、また、Σ3の分布割合を60%以上と定めた。
また、Ti−Cr複合炭窒化物層の平均層厚は、1μm未満ではすぐれた高温特性を発揮することができず、一方、平均層厚が5μmを超えると、隣接するTiCN層との十分な付着強度を確保することができなくなることから、その平均層厚を1〜5μmと定めた。
(B) Ti-Cr composite carbonitride layer Ti-Cr composite carbonitride layer has the excellent high-temperature hardness and excellent high-temperature strength, this property is a CrCl 3 to the reaction gas 0.02 In the constituent atomic shared lattice distribution graph, as a result of chemical vapor deposition by adding at a volume percentage, the Cr content in the deposited layer is 1 to 10 atomic% as a percentage of the total amount with Ti. It is obtained when the distribution ratio of Σ3 is 60% or more. On the other hand, when the distribution ratio of Σ3 is less than 60%, the effect of improving high-temperature strength is small, and in high-speed, high-feed, high-cut milling processing, It is inevitable that chipping occurs in the layer, and excellent wear resistance cannot be exhibited. Therefore, the Cr content ratio (Cr / (Ti + Cr)) to the total amount of Ti and Cr is 0.01 to 0. 1 (provided that the atomic ratio) defined as, also, was defined as 60% or more a distribution ratio of [sum] 3.
In addition, when the average layer thickness of the Ti—Cr composite carbonitride layer is less than 1 μm, excellent high temperature characteristics cannot be exhibited. On the other hand, when the average layer thickness exceeds 5 μm, the Ti—Cr composite carbonitride layer is sufficiently thick with the adjacent TiCN layer. Since the adhesion strength could not be ensured, the average layer thickness was determined to be 1 to 5 μm.

(c)Ti系化合物積層
上記TiCN層と上記Ti−Cr複合炭窒化物層を、少なくとも3層以上交互に積層し、合計平均層厚が5〜15μmとなるように化学蒸着でTi系化合物積層を形成するが、Ti系化合物積層の合計平均層厚が5μm未満では、高速高送り高切り込みミーリング加工において十分な耐摩耗性を発揮することができず、一方、合計平均層厚が15μmを超えると、チッピングや異常摩耗が発生し易くなるため、Ti系化合物積層の合計平均層厚を5〜15μmと定めた。
(C) Ti-based compound stacking At least three TiCN layers and Ti-Cr composite carbonitride layers are alternately stacked, and Ti-based compound stacking is performed by chemical vapor deposition so that the total average layer thickness is 5 to 15 μm. However, if the total average layer thickness of the Ti-based compound laminate is less than 5 μm, sufficient wear resistance cannot be exhibited in high-speed, high-feed, high-cut milling processing, while the total average layer thickness exceeds 15 μm. Then, since chipping and abnormal wear are likely to occur, the total average layer thickness of the Ti-based compound stack is set to 5 to 15 μm.

(d)Al−Cr複合酸化物層
アルミニウムとクロムの複合酸化物層からなる上部層は、そのAl成分によって、すぐれた高温硬さと耐熱性を、また、そのCr成分によって、すぐれた高温強度を備え、被覆工具の耐チッピング性、耐摩耗性向上に寄与するが、複合酸化物層(Al−Cr複合酸化物層)におけるCr成分の含有割合は、層中に含有するAlとCrの合量に占める割合(=Cr/(Al+Cr))で、0.01〜0.1(但し、原子比)の範囲内のものとする。Al−Cr複合酸化物層におけるクロム成分の含有割合を示すこの値が0.01未満であると、上部層の高温強度の向上の効果が少なく、一方、この値が0.1を超えると、上部層におけるアルミニウム成分量の相対的な減少により高温硬さ、耐熱性の低下が生じ、その結果として耐摩耗性劣化の傾向がみられるので、Al−Cr複合酸化物層におけるクロム成分の含有割合(原子比で換算したCr/(Al+Cr)の値)を、上記のとおり、0.01〜0.1の範囲内の値とする。
また、その平均層厚が0.5μm未満では、所望のすぐれた切削性能を長期に亘って発揮させることができず、一方その平均層厚が5μmを越えて厚くなりすぎると、チッピングが発生し易くなることから、その平均層厚を0.5〜5μmと定めた。
(D) Al—Cr composite oxide layer The upper layer made of a composite oxide layer of aluminum and chromium has excellent high-temperature hardness and heat resistance due to its Al component, and excellent high-temperature strength due to its Cr component. Although it contributes to chipping resistance and wear resistance improvement of the coated tool, the content ratio of Cr component in the composite oxide layer (Al-Cr composite oxide layer) is the total amount of Al and Cr contained in the layer The ratio (= Cr / (Al + Cr)) in the range of 0.01 to 0.1 (however, the atomic ratio). When this value indicating the content ratio of the chromium component in the Al—Cr composite oxide layer is less than 0.01, the effect of improving the high-temperature strength of the upper layer is small, whereas when this value exceeds 0.1, The relative decrease in the amount of aluminum component in the upper layer causes a decrease in high-temperature hardness and heat resistance. As a result, there is a tendency for wear resistance to deteriorate, so the content of chromium component in the Al-Cr composite oxide layer (Cr / (Al + Cr) value converted by atomic ratio) is set to a value within the range of 0.01 to 0.1 as described above.
If the average layer thickness is less than 0.5 μm, the desired excellent cutting performance cannot be exhibited over a long period of time. On the other hand, if the average layer thickness exceeds 5 μm, chipping occurs. Since it becomes easy, the average layer thickness was determined to be 0.5 to 5 μm.

(e)中間層
炭酸化チタン(TiCO)層、窒酸化チタン(TiNO)層および炭窒酸化チタン(TiCNO)層のうちの1種または2種以上からなる合計平均層厚0.2〜1μmの中間層を、TiCN層およびTi−Cr複合炭窒化物層からなる上記Ti系化合物積層と、上記Al−Cr複合酸化物層との間に介在形成する。上記中間層は、上記Ti系化合物積層と上記Al−Cr複合酸化物層のいずれに対しても密着性にすぐれ付着強度も大きいため、Ti系化合物積層とAl−Cr複合酸化物層間の接合強度を高め、その結果、硬質被覆層全体としての高温強度を高め耐チッピング性を向上させる効果があるが、その合計平均層厚が0.2μm未満では接合強度の向上がみられず、また、合計平均層厚が1μmを超えると、チッピングなどの異常損傷が生じやすくなることから、中間層の合計平均層厚を0.2〜1μmと定めた。
(E) Intermediate layer A total average layer thickness of 0.2 to 1 μm consisting of one or more of a titanium carbonate (TiCO) layer, a titanium nitride oxide (TiNO) layer and a titanium carbonitride oxide (TiCNO) layer An intermediate layer is interposed between the Ti-based compound stack composed of a TiCN layer and a Ti—Cr composite carbonitride layer and the Al—Cr composite oxide layer. Since the intermediate layer has excellent adhesion and high adhesion strength to both the Ti-based compound laminate and the Al—Cr composite oxide layer, the bonding strength between the Ti-based compound laminate and the Al—Cr composite oxide layer is high. As a result, there is an effect of increasing the high-temperature strength of the hard coating layer as a whole and improving the chipping resistance, but if the total average layer thickness is less than 0.2 μm, no improvement in bonding strength is observed, and the total When the average layer thickness exceeds 1 μm, abnormal damage such as chipping is likely to occur. Therefore, the total average layer thickness of the intermediate layer is set to 0.2 to 1 μm.

なお、被覆工具の切削後の使用コーナーの識別を容易にする目的で、硬質被覆層の上層に、金色を有するTiN層を被覆することが一般的に知られているが、本発明被覆工具においても、使用コーナー識別の目的で、Al−Cr複合酸化物層の上層に、TiN層を被覆してもよい。その際のTiN層の被覆層厚は0.2〜1μmで十分である。
また、近年、硬質被覆層を形成後、物理的な手法、具体的には砥石、ナイロン製等のブラシ、SiC、AlおよびZrO粒子等をメディアとして使用する乾式あるいは湿式ブラスト処理等により、硬質被覆層の表面を平滑化し、耐溶着性を向上させることが知られているが、本発明被覆工具に対してこれを適用することも勿論可能である。
It is generally known that a TiN layer having a gold color is coated on the hard coating layer for the purpose of facilitating identification of a use corner after cutting of the coated tool. Alternatively, a TiN layer may be coated on the upper layer of the Al—Cr composite oxide layer for the purpose of identifying the use corner. In this case, the thickness of the coating layer of the TiN layer is sufficient to be 0.2 to 1 μm.
Also, in recent years, after forming a hard coating layer, a physical method, specifically, a dry or wet blasting process using a grinding wheel, a brush made of nylon, etc., SiC, Al 2 O 3 and ZrO 2 particles as a medium, etc. Thus, it is known that the surface of the hard coating layer is smoothed and the welding resistance is improved, but it is of course possible to apply this to the coated tool of the present invention.

この発明の被覆工具は、硬質被覆層が、Ti−Cr複合炭窒化物層と炭窒化チタン層の交互積層構造からなるTi系化合物積層の下部層と、Al−Cr複合酸化物層からなる上部層とで構成され(請求項1)、あるいは、Ti系化合物積層とAl−Cr複合酸化物層との間に中間層を介在させたものとして構成され(請求項2)、さらに、前記Ti−Cr複合炭窒化物層が、Tiとの合量に占める割合で1〜10原子%のCrを含有し、構成原子共有格子点分布グラフでのΣ3の分布割合が60%以上のきわめて高いものとして構成されている(請求項3)ので、各種の鋼、ステンレス鋼および鋳鉄などの通常条件でのミーリング加工は勿論のこと、特に、機械的・熱的負荷が大きく、かつ高い発熱を伴う高速高送り、高切り込み切削でも、すぐれた耐チッピング性、耐摩耗性を示し、長期に亘ってすぐれた切削性能を発揮するものである。   In the coated tool of the present invention, the hard coating layer includes a lower layer of a Ti-based compound stack composed of an alternately stacked structure of a Ti—Cr composite carbonitride layer and a titanium carbonitride layer, and an upper portion composed of an Al—Cr composite oxide layer. (Claim 1), or an intermediate layer interposed between the Ti-based compound stack and the Al—Cr composite oxide layer (Claim 2), and the Ti— Assuming that the Cr composite carbonitride layer contains 1 to 10 atomic% of Cr in the ratio to the total amount of Ti, and the distribution ratio of Σ3 in the constituent atomic shared lattice distribution graph is extremely high of 60% or more. Since it is configured (Claim 3), not only milling under normal conditions such as various steels, stainless steels and cast irons, in particular, high speed and high mechanical load, high heat load and high heat generation. Even with feed and high cutting depth, Gres chipping resistance, shows the wear resistance, is to exhibit excellent cutting performance over a long period of time.

つぎに、この発明の被覆工具を実施例により具体的に説明する。   Next, the coated tool of the present invention will be specifically described with reference to examples.

原料粉末として、いずれも1〜3μmの平均粒径を有するWC粉末、TiC粉末、TaC粉末、NbC粉末、Cr32粉末、TiN粉末、TaN粉末、およびCo粉末を準備し、これら原料粉末を、表1に示される配合組成に配合し、さらにワックスを加えてアルコール中で10時間ボールミル混合し、減圧乾燥した後、98MPaの圧力で所定形状の圧粉体にプレス成形し、この圧粉体を5Paの真空中、1370〜1470℃の範囲内の所定の温度に1時間保持の条件で真空焼結し、焼結後、切刃部に幅0.15mm、角度20度のチャンフォーホーニング加工することによりISO・SEEN1203AFTN1に規定するスローアウェイチップ形状をもったWC基超硬合金製の工具基体A〜Fをそれぞれ製造した。 As raw material powders, WC powder, TiC powder, TaC powder, NbC powder, Cr 3 C 2 powder, TiN powder, TaN powder, and Co powder all having an average particle diameter of 1 to 3 μm are prepared. Then, blended into the composition shown in Table 1, added with wax, ball mill mixed in alcohol for 10 hours, dried under reduced pressure, and then press molded into a compact of a predetermined shape at a pressure of 98 MPa. Is vacuum-sintered at a predetermined temperature in the range of 1370 to 1470 ° C. for 1 hour in a vacuum of 5 Pa, and after sintering, the cutting edge portion has a width of 0.15 mm and an angle of 20 degrees Chamfor Honing As a result, tool bases A to F made of a WC-based cemented carbide having a throwaway tip shape specified in ISO · SEEN1203AFTN1 were produced.

ついで、これらの工具基体A〜F表面に、通常の化学蒸着装置を用いて、
反応ガス組成:容量%で、TiCl:2〜10%、CHCN:1〜5%、N2:10〜30%、H2:残り、の範囲内の所定組成、
反応雰囲気温度:800〜930℃、の範囲内の所定温度、
反応雰囲気圧力:15〜25kPa、の範囲内の所定圧力、
の条件(表3)で、表7に示される目標平均層厚のTiCN層を蒸着形成し、ついで、表2に示される条件かつ表7に示される目標平均層厚でTi−Cr複合炭窒化物層を蒸着形成し、TiCN層とTi−Cr複合炭窒化物層の交互積層からなるTi系化合物積層を下部層として蒸着形成し、つぎに、表4に示される条件でかつ表7に示される目標平均層厚でAl−Cr複合酸化物層を上部層として蒸着形成し、さらに、表5に示される条件かつ表7に示される目標層厚で中間層を蒸着形成することにより、本発明被覆工具1〜6を製造した。
なお、表2でいう「目標Cr含有割合」は、原子比で表したCr/(Ti+Cr)の値、また、表4でいう「目標Cr含有割合」は、原子比で表したCr/(Al+Cr)の値である。
Next, on the surface of these tool bases A to F, using a normal chemical vapor deposition apparatus,
Reaction gas composition: by volume%, TiCl 4: 2~10%, CH 3 CN: 1~5%, N 2: 10~30%, H 2: remainder, a predetermined composition within the range of,
Reaction atmosphere temperature: a predetermined temperature within a range of 800 to 930 ° C,
Reaction atmospheric pressure: a predetermined pressure within a range of 15 to 25 kPa,
Then, a TiCN layer having a target average layer thickness shown in Table 7 is formed by vapor deposition under the following conditions (Table 3), and then Ti—Cr composite carbonitriding is performed under the conditions shown in Table 2 and the target average layer thickness shown in Table 7. The material layer is formed by vapor deposition, and a Ti-based compound layer composed of alternating layers of TiCN layers and Ti—Cr composite carbonitride layers is deposited as a lower layer. Next, the conditions shown in Table 4 and Table 7 are shown. By depositing an Al—Cr composite oxide layer as an upper layer with a target average layer thickness to be formed and further forming an intermediate layer with the conditions shown in Table 5 and the target layer thickness shown in Table 7 by the present invention. Coated tools 1-6 were produced.
Note that “target Cr content ratio” in Table 2 is the value of Cr / (Ti + Cr) expressed in atomic ratio, and “target Cr content ratio” in Table 4 is Cr / (Al + Cr) expressed in atomic ratio. ) Value.

また、比較の目的で、Ti−Cr複合炭窒化物層の代わりにTiN層またはTiC層を、表6に示される条件かつ表8に示される目標平均層厚で形成し、さらに、TiCN層については上記本発明被覆工具のTiCN層と同一の条件(表3)かつ同一の目標平均層厚で形成し、さらに、表5に示される条件かつ表8に示される目標層厚で中間層を蒸着形成することにより、従来被覆工具1〜6をそれぞれ製造した。
(Al−Cr複合酸化物層、中間層については上記本発明被覆工具1〜6と同一の条件かつ同一の目標平均層厚で形成した)。
For the purpose of comparison, instead of the Ti—Cr composite carbonitride layer, a TiN layer or a TiC layer is formed under the conditions shown in Table 6 and the target average layer thickness shown in Table 8. Further, regarding the TiCN layer Is formed under the same conditions (Table 3) and the same target average layer thickness as the TiCN layer of the above-mentioned coated tool of the present invention, and the intermediate layer is deposited under the conditions shown in Table 5 and the target layer thickness shown in Table 8. By forming, conventionally coated tools 1 to 6 were respectively produced.
(The Al—Cr composite oxide layer and the intermediate layer were formed under the same conditions and the same target average layer thickness as those of the present invention coated tools 1 to 6).

ついで、上記の本発明被覆工具の硬質被覆層の下部層を構成するTi−Cr複合炭窒化物層、および、本発明被覆工具および従来被覆工具の硬質被覆層を構成するTiCN層について、電界放出型走査電子顕微鏡を用いて、構成原子共有格子点分布グラフを作成した。
すなわち、上記構成原子共有格子点分布グラフは、上記本発明Ti−Cr複合炭窒化物層、および、従来TiCN層の表面をそれぞれ研磨面とした状態で、電界放出型走査電子顕微鏡の鏡筒内にセットし、前記研磨面に70度の入射角度で15kVの加速電圧の電子線を1nAの照射電流で、前記表面研磨面の測定範囲内に存在する結晶粒個々に照射して、電子後方散乱回折像装置を用い、30×50μmの領域を0.1μm/stepの間隔で、前記表面研磨面の法線に対して、前記結晶粒の結晶面である(001)面および(011)面の法線がなす傾斜角を測定し、この結果得られた測定傾斜角に基づいて、相互に隣接する結晶粒の界面で、前記構成原子のそれぞれが前記結晶粒相互間で1つの構成原子を共有する格子点(構成原子共有格子点)の分布を算出し、前記構成原子共有格子点間に構成原子を共有しない格子点がN個(NはNaCl型面心立方晶の結晶構造上2以上の偶数となる)存在する構成原子共有格子点形態をΣN+1で表した場合、個々のΣN+1がΣN+1全体(ただし、頻度の関係で上限値を28とする)に占める分布割合を求めることにより作成した。
Next, the field emission of the Ti—Cr composite carbonitride layer constituting the lower layer of the hard coating layer of the above-described coated tool of the present invention and the TiCN layer constituting the hard coated layer of the coated tool of the present invention and the conventional coated tool is described. Using a scanning electron microscope, a constituent atom sharing lattice distribution graph was created.
In other words, the constituent atomic shared lattice point distribution graph is shown in the column of the field emission scanning electron microscope in a state where the surfaces of the Ti-Cr composite carbonitride layer of the present invention and the conventional TiCN layer are respectively polished surfaces. Electron backscattering is performed by irradiating the polishing surface with an electron beam having an acceleration voltage of 15 kV at an incident angle of 70 degrees with an irradiation current of 1 nA on each crystal grain within the measurement range of the surface polishing surface. Using a diffraction image apparatus, a region of 30 × 50 μm is spaced at a spacing of 0.1 μm / step and the (001) plane and (011) plane, which are crystal planes of the crystal grains, with respect to the normal line of the surface polishing plane Measure the tilt angle formed by the normal, and based on the measured tilt angle, each of the constituent atoms shares one constituent atom between the crystal grains at the interface between the adjacent crystal grains. Lattice points (constituent atom sharing (Distribution point) distribution, and there are N lattice points that do not share constituent atoms between the constituent atomic shared lattice points (N is an even number of 2 or more in the crystal structure of the NaCl-type face-centered cubic crystal) When the atomic shared lattice point form is represented by ΣN + 1, it was created by determining the distribution ratio of each ΣN + 1 to the entire ΣN + 1 (however, the upper limit value is 28 due to frequency).

この結果得られた本発明Ti−Cr複合炭窒化物層の構成原子共有格子点分布グラフにおいて、ΣN+1全体(Nは2〜28の範囲内のすべての偶数)に占めるΣ3の分布割合をそれぞれ表7に示した。
また、比較のために、本発明被覆工具および従来被覆工具のTiCN層の構成原子共有格子点分布グラフにおいて、ΣN+1全体(Nは2〜28の範囲内のすべての偶数)に占めるΣ3の分布割合をそれぞれ表8に示した。
In the constituent atomic shared lattice point distribution graph of the Ti—Cr composite carbonitride layer of the present invention obtained as a result, the distribution ratio of Σ3 occupying the entire ΣN + 1 (N is an even number within the range of 2 to 28) is shown. 7 shows.
For comparison, the distribution ratio of Σ3 occupying the entire ΣN + 1 (N is all even numbers in the range of 2 to 28) in the constituent atomic shared lattice point distribution graph of the TiCN layer of the present coated tool and the conventional coated tool. Is shown in Table 8.

上記の各種の構成原子共有格子点分布グラフにおいて、表7、8にそれぞれ示される通り、本発明被覆工具1〜6のTi−Cr複合炭窒化物層は、いずれもΣ3の占める分布割合が60%以上である構成原子共有格子点分布グラフを示すのに対して、従来被覆工具1〜6の従来TiCN層は、いずれもΣ3の分布割合が30%未満の構成原子共有格子点分布グラフを示すものであった。
なお、図3は、本発明被覆工具4のうちA−4の条件にて形成したTi−Cr複合炭窒化物層の構成原子共有格子点分布グラフ、図4は、従来被覆工具6のうち、a―5の条件にて形成した従来TiCN層の構成原子共有格子点分布グラフをそれぞれ示すものである。
In the above-mentioned various constituent atomic share lattice point distribution graphs, as shown in Tables 7 and 8, the Ti—Cr composite carbonitride layers of the present coated tools 1 to 6 each have a distribution ratio of Σ3 of 60. %, The conventional TiCN layer of the conventional coated tools 1 to 6 shows a constituent atom shared lattice point distribution graph in which the distribution ratio of Σ3 is less than 30%. It was a thing.
3 is a constituent atomic shared lattice distribution graph of the Ti—Cr composite carbonitride layer formed under the condition A-4 in the coated tool 4 of the present invention, and FIG. FIG. 5 shows a constituent atomic shared lattice point distribution graph of a conventional TiCN layer formed under the conditions of a-5.

さらに、上記の本発明被覆工具1〜6および従来被覆工具1〜6について、これらの硬質被覆層の構成層をオージェ分光分析装置を用いて観察(層の縦断面を観察)したところ、目標組成と実質的に同じ組成を有することが確認され、また、これらの被覆工具の硬質被覆層の構成層の厚さを、走査型電子顕微鏡を用いて測定(同じく縦断面測定)したところ、いずれも目標層厚と実質的に同じ平均層厚(5点測定の平均値)を示した。   Further, for the above-described coated tools 1 to 6 of the present invention and the conventional coated tools 1 to 6, the constituent layers of these hard coating layers were observed using an Auger spectroscopic analyzer (the longitudinal section of the layers was observed). And the thickness of the constituent layer of the hard coating layer of these coated tools was measured using a scanning electron microscope (same longitudinal section measurement). The average layer thickness (average value of 5-point measurement) substantially the same as the target layer thickness was shown.

まず、上記の本発明被覆工具1〜6および従来被覆工具1〜6については、次の切削条件A〜Cにより、単刃での正面フライス加工を実施した。
[切削条件A]
被削材: JIS・ SNCM439ブロック材、
切削速度: 350 m/min、
切り込み: 4 mm、
一刃送り量: 0.42 mm/刃、
切削時間: 5 分、
の条件での合金鋼の湿式高速高切り込み高送り切削試験(通常の切削速度、切り込み、送りは、それぞれ、180m/min、1.5mm、0.2mm/刃)、
[切削条件B]
被削材: JIS・SUS316ブロック材、
切削速度: 300 m/min、
切り込み: 3.5 mm、
一刃送り量: 0.4 mm/刃、
切削時間: 3 分、
の条件でのステンレス鋼の湿式高速高切り込み高送り切削試験(通常の切削速度、切り込み、送りは、それぞれ、150m/min、1.5mm、0.2mm/刃)、
[切削条件C]
被削材: JIS・FCD450ブロック、
切削速度: 380 m/min、
切り込み: 4 mm、
送り: 0.42 mm/刃、
切削時間: 5 分、
の条件でのダクタイル鋳鉄の乾式高速高切り込み高送り切削試験(通常の切削速度、切り込み、送りは、それぞれ、180m/min、1.5mm、0.2mm/刃)、
を行い、上記の各切削試験における切刃の逃げ面摩耗幅を測定し、この測定結果を表9に示した。
First, for the above-described inventive coated tools 1 to 6 and conventional coated tools 1 to 6, face milling with a single blade was performed under the following cutting conditions A to C.
[Cutting conditions A]
Work material: JIS / SNCM439 block material,
Cutting speed: 350 m / min,
Cutting depth: 4 mm,
Single blade feed amount: 0.42 mm / tooth,
Cutting time: 5 minutes,
Wet high-speed, high-cut, high-feed cutting test (normal cutting speed, cutting, feed are 180 m / min, 1.5 mm, 0.2 mm / blade, respectively)
[Cutting conditions B]
Work material: JIS / SUS316 block material,
Cutting speed: 300 m / min,
Cutting depth: 3.5 mm,
Single blade feed rate: 0.4 mm / tooth,
Cutting time: 3 minutes,
Stainless steel wet high-speed high-cut high-feed cutting test (normal cutting speed, cutting and feed are 150 m / min, 1.5 mm, and 0.2 mm / blade, respectively),
[Cutting conditions C]
Work material: JIS / FCD450 block,
Cutting speed: 380 m / min,
Cutting depth: 4 mm,
Feed: 0.42 mm / tooth,
Cutting time: 5 minutes,
Ductile cast iron dry high-speed high-cut high-feed cutting test (normal cutting speed, cutting and feed are 180 m / min, 1.5 mm, and 0.2 mm / blade, respectively),
The flank wear width of the cutting edge in each of the above cutting tests was measured, and the measurement results are shown in Table 9.

Figure 2008093754
Figure 2008093754

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Figure 2008093754
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Figure 2008093754
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Figure 2008093754
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Figure 2008093754
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Figure 2008093754
Figure 2008093754

Figure 2008093754
Figure 2008093754

表9に示される結果から、本発明被覆工具1〜6は、硬質被覆層の下部層が、Ti−Cr複合炭窒化物層と炭窒化チタン層の交互積層構造からなるTi系化合物積層で形成され、かつ、前記Ti−Cr複合炭窒化物層は、Tiとの合量に占める割合で1〜10原子%のCrを含有し、構成原子共有格子点分布グラフでのΣ3の分布割合が60%以上のきわめて高いものとして構成され、さらに、硬質被覆層の上部層が、すぐれた高温硬さ、耐熱性、高温強度を備えたAl−Cr複合酸化物層から構成され、しかも、前記Ti−Cr複合炭窒化物層と前記Al−Cr複合酸化物層は、中間層を介して接合強度の非常に高い硬質被覆層を構成しているので、機械的・熱的負荷が大きく、しかも、高い発熱を伴う各種の鋼、ステンレス鋼および鋳鉄などの高速高送り、高切り込みミーリング切削において、硬質被覆層がすぐれた耐チッピング性とすぐれた耐摩耗性を発揮するのに対して、硬質被覆層の下部層が従来TiCN層と窒化チタン層の交互積層構造あるいはTiCN層と炭化チタン層の交互積層構造として形成された従来被覆工具1〜6においては、高速高送り、高切り込みミーリング切削の激しい機械的・熱的負荷に耐えられず、硬質被覆層にはチッピングが発生し、また摩耗も促進され、これが原因となり比較的短時間で使用寿命に至ることが明らかである。   From the results shown in Table 9, the coated tools 1 to 6 of the present invention are formed of a Ti-based compound laminate in which the lower layer of the hard coating layer is composed of an alternately laminated structure of a Ti—Cr composite carbonitride layer and a titanium carbonitride layer. In addition, the Ti—Cr composite carbonitride layer contains 1 to 10 atomic% of Cr as a proportion of the total amount with Ti, and the distribution ratio of Σ3 in the constituent atomic shared lattice distribution graph is 60. %, And the upper layer of the hard coating layer is composed of an Al—Cr composite oxide layer having excellent high temperature hardness, heat resistance and high temperature strength, and the Ti— Since the Cr composite carbonitride layer and the Al—Cr composite oxide layer constitute a hard coating layer having a very high bonding strength through an intermediate layer, the mechanical and thermal load is large and high. Various steel, stainless steel and cast iron with heat generation In any high-speed, high-feed, high-cut milling cutting, the hard coating layer exhibits excellent chipping resistance and excellent wear resistance, whereas the lower layer of the hard coating layer has a conventional alternating TiCN layer and titanium nitride layer. The conventional coated tools 1 to 6 formed as a laminated structure or an alternately laminated structure of TiCN layers and titanium carbide layers cannot withstand the high mechanical and thermal loads of high-speed, high-feed, high-cut milling, and hard coating layers. It is clear that chipping occurs and wear is accelerated, which leads to a service life in a relatively short time.

上述のように、この発明の被覆工具は、各種の鋼、ステンレス鋼および鋳鉄などの通常の条件でのミーリング加工は勿論のこと、特に、機械的・熱的負荷が大きく、かつ高い発熱を伴う高速高送り高切り込みの高速重切削条件でも、すぐれた耐チッピング性、耐摩耗性を示し、長期に亘ってすぐれた切削性能を発揮するものであるから、切削装置の高性能化ならびに切削加工の省力化および省エネ化、さらに低コスト化に十分満足に対応できるものである。   As described above, the coated tool of the present invention is not only milled under normal conditions such as various types of steel, stainless steel, and cast iron, and particularly has a large mechanical and thermal load and is accompanied by high heat generation. Even under high-speed, high-feed, high-cut high-speed heavy cutting conditions, it exhibits excellent chipping resistance and wear resistance, and exhibits excellent cutting performance over a long period of time. It can be used satisfactorily for labor saving, energy saving, and cost reduction.

硬質被覆層の従来TiCN層が有するNaCl型面心立方晶の結晶構造を示す模式図である。It is a schematic diagram which shows the crystal structure of the NaCl type face centered cubic crystal which the conventional TiCN layer of a hard coating layer has. NaCl型面心立方晶の結晶構造を有する結晶粒の(001)面および(011)面の傾斜角の測定態様を示す概略説明図である。It is a schematic explanatory drawing which shows the measurement aspect of the inclination angle of the (001) plane and the (011) plane of the crystal grain which has a crystal structure of a NaCl type face centered cubic crystal. 本発明被覆工具4の形成条件A−4で形成したTi−Cr複合炭窒化物層の構成原子共有格子点分布グラフである。It is a constituent atom shared lattice point distribution graph of the Ti-Cr compound carbonitride layer formed on formation condition A-4 of the present invention covering tool 4. 従来被覆工具6の形成条件a−5で形成した従来TiCN層の構成原子共有格子点分布グラフである。It is a constituent atom shared lattice point distribution graph of the conventional TiCN layer formed on the formation condition a-5 of the conventional coated tool 6.

Claims (3)

炭化タングステン基超硬合金または炭窒化チタン基サーメットで構成された工具基体の表面に、下部層と上部層からなる硬質被覆層を蒸着形成した表面被覆切削工具において、
上記下部層は、
(a)1〜5μmの平均層厚を有する炭窒化チタン層、
(b)1〜5μmの平均層厚を有し、かつ、チタンとクロムの合量に対するクロムの含有割合(Cr/(Ti+Cr))が、原子比で0.01〜0.1であるチタンとクロムの複合炭窒化物層、
上記(a)および(b)を少なくとも3層以上交互に積層し、合計平均層厚が5〜15μmとなるよう化学蒸着したチタン系化合物積層、
上記上部層は、
(c)0.5〜5μmの平均層厚を有し、かつ、アルミニウムとクロムの合量に対するクロムの含有割合(Cr/(Al+Cr))が、原子比で0.01〜0.1であるアルミニウムとクロムの複合酸化物層、
からなる硬質被覆層を設けたことを特徴とする硬質被覆層がすぐれた耐チッピング性を発揮する表面被覆切削工具。
In a surface-coated cutting tool in which a hard coating layer composed of a lower layer and an upper layer is vapor-deposited on the surface of a tool base composed of a tungsten carbide-based cemented carbide or a titanium carbonitride-based cermet,
The lower layer is
(A) a titanium carbonitride layer having an average layer thickness of 1 to 5 μm,
(B) Titanium having an average layer thickness of 1 to 5 μm and a chromium content ratio (Cr / (Ti + Cr)) of 0.01 to 0.1 in terms of atomic ratio relative to the total amount of titanium and chromium Chromium composite carbonitride layer,
(A) and (b) at least three or more layers are alternately stacked, and a titanium-based compound layer is formed by chemical vapor deposition so that the total average layer thickness is 5 to 15 μm.
The upper layer is
(C) It has an average layer thickness of 0.5 to 5 μm, and the content ratio of chromium to the total amount of aluminum and chromium (Cr / (Al + Cr)) is 0.01 to 0.1 in atomic ratio. A complex oxide layer of aluminum and chromium,
A surface-coated cutting tool that exhibits excellent chipping resistance, wherein the hard coating layer is provided with a hard coating layer.
請求項2記載の表面被覆切削工具において、
上記チタン系化合物積層からなる下部層と、上記アルミニウムとクロムの複合酸化物層からなる上部層との間に、炭酸化チタン層、窒酸化チタン層および炭窒酸化チタン層のうちの1種または2種以上からなる合計平均層厚0.2〜1μmの中間層を介在させたことを特徴とする請求項1記載の表面被覆切削工具。
The surface-coated cutting tool according to claim 2,
One of a titanium carbonate layer, a titanium oxynitride layer and a titanium carbonitride oxide layer between the lower layer made of the titanium-based compound laminate and the upper layer made of the composite oxide layer of aluminum and chromium, or The surface-coated cutting tool according to claim 1, wherein an intermediate layer having a total average layer thickness of 0.2 to 1 µm is interposed.
請求項1乃至2記載の表面被覆切削工具において、
上記(b)のチタンとクロムの複合炭窒化物層は、電界放出型走査電子顕微鏡を用い、表面研磨面の測定範囲内に存在する結晶粒個々に電子線を照射して、前記表面研磨面の法線に対して、前記結晶粒の結晶面である(001)面および(011)面の法線がなす傾斜角を測定し、この場合前記結晶粒は、格子点にチタンとクロムと炭素と窒素からなる構成原子がそれぞれ存在するNaCl型面心立方晶の結晶構造を有し、この結果得られた測定傾斜角に基づいて、相互に隣接する結晶粒の界面で、前記構成原子のそれぞれが前記結晶粒相互間で1つの構成原子を共有する格子点(構成原子共有格子点)の分布を算出し、前記構成原子共有格子点間に構成原子を共有しない格子点がN個(NはNaCl型面心立方晶の結晶構造上2以上の偶数となる)存在する構成原子共有格子点形態をΣN+1で表した場合、個々のΣN+1がΣN+1全体(ただし、頻度の関係で上限値を28とする)に占める分布割合を示す構成原子共有格子点分布グラフにおいて、いずれもΣ3に最高ピークが存在し、かつ前記Σ3のΣN+1全体に占める分布割合が60%以上である構成原子共有格子点分布グラフを示すチタンとクロムの複合炭窒化物層であることを特徴とする請求項1乃至2のいずれか一項に記載の表面被覆切削工具。
The surface-coated cutting tool according to claim 1 or 2,
The composite carbonitride layer of titanium and chromium of (b) is irradiated with an electron beam on each crystal grain existing within the measurement range of the surface polishing surface using a field emission scanning electron microscope, and the surface polishing surface The tilt angle formed by the normal lines of the (001) plane and (011) plane, which are crystal planes of the crystal grains, is measured. In this case, the crystal grains have titanium, chromium, and carbon at lattice points. Each of the constituent atoms has a crystal structure of NaCl type face centered cubic crystal in which constituent atoms composed of nitrogen and nitrogen are present, respectively, at the interface between adjacent crystal grains based on the measured tilt angle. Calculates the distribution of lattice points that share one constituent atom between the crystal grains (constituent atom shared lattice points), and N lattice points that do not share constituent atoms between the constituent atom shared lattice points (N is N An even number of 2 or more in the crystal structure of the NaCl type face centered cubic crystal When the configuration of existing constituent atomic shared lattice points is represented by ΣN + 1, the constituent atomic shared lattice point distribution graph showing the distribution ratio of each ΣN + 1 in the entire ΣN + 1 (however, the upper limit is 28 in terms of frequency) In any of the above, it is a composite carbonitride layer of titanium and chromium that shows a constituent atomic shared lattice point distribution graph in which the highest peak exists in Σ3 and the distribution ratio of the Σ3 in the entire ΣN + 1 is 60% or more. The surface-coated cutting tool according to any one of claims 1 to 2, wherein the surface-coated cutting tool is characterized.
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