Coated cutting tool

CROSS REFERENCE TO RELATED APPLICATION

[0001] This application claims priority under 35 U.S.C. §119 from Japanese Patent Application Nos. 2000-390 038, 390 039 and 390 040, all filed on Dec. 22, 2000, and 2001-054 097 and 054 098, both filed on Feb. 28, 2001, which are incorporated herein by reference in their entirety.

BACKGROUND OF THE INVENTION

[0002] 1. Field of the Invention

[0003] The present invention relates to a coated cutting tool in which a hard coating layer has excellent strength and hardness at high temperature. Therefore, it has high wear resistance even when it is applied to a high-speed cutting operation of ferrous materials such as steel and cast iron.

[0004] 2. Discussion of the Background

[0005] Many kinds of conventional cutting tools are known. Throw-away inserts are used in various cutting operations such as turning or milling of steels and cast irons by flexibly attaching on bite holders, face milling cutter bodies and end-milling cutter bodies. Twist drills that are used for a drilling of the above-mentioned work materials are also well known. Recently, micro drills are extensively used in a drilling process of printed circuit boards. Furthermore, solid end-milling cutters, used in various operations such as face milling, groove milling and shoulder milling, are also widely used, for example, in mold machining processes.

[0006] Furthermore, in general, as a material constituting the above-mentioned putting tools, a coated cutting tool which comprises a hard coating, such as titanium nitride (hereinafter referred to as TiN), and/or titanium carbonitride (hereinafter referred to as TiCN), having 0.5-10 μm for the average layer thickness, on the surface of a hard material substrate, such as tungsten carbide-based cemented carbide (hereinafter referred to as cemented carbide), titanium carbonitride-based cermet (hereinafter referred to as cermet) and a high speed steel, is well known, and it is also known that said coated cutting tool is used for continuous cutting and to interrupt cutting of steels and cast irons.

[0007] As one of the hard coating layers of the above-mentioned coated cutting tool, according to Japanese Patent Laid Open Application No. 62-56565, it is known that a titanium-aluminum nitride [(Ti, Al) N] layer is coated under the following conditions, that is, for example, at first, in a condition of about 3 Pa and 500° C. inside the chamber, an arc discharge is generated between an anode electrode and a cathode electrode (an evaporation source) in which an Ti-Al alloy having predetermined composition is set, by loading electrical potential of 35 V and electrical current of 90 A, and after that, nitrogen gas is introduced as a reaction gas into the chamber, and the bias potential of, for example 200 V, is applied to the substrate, by using an arc ion plating system which is one of the physical vapor deposition processes having equipment shown in FIG. 1.

[0008] Moreover, it is known that the residual compressive stress is given to the hard coating deposited by the physical vapor deposition process in this way, and the value of said compressive stress can be changed by selecting the coating conditions, such as the above-mentioned bias potential. It is also well known that the resistance against breakage, in other words, toughness, of said coated cutting tool can be raised by controlling this compressive stress suitably.

[0009] In addition, according to Japanese Patent Laid Open Application No. 1-240215, it is also known that other composite hard coatings, such as a composite nitride of titanium and zirconium [hereinafter referred to as (Ti, Zr)N] can be formed by utilizing another metal alloy target such as a Ti-Zr alloy as the evaporation source instead of above-mentioned Ti-Al alloy. These hard coatings can also raise the resistance against breakage of the coated cutting tool by suitably controlling the residual compressive stress of the coating like said (Ti, Al)N layer.

[0010] In recent years, there has been an increasing demand for labor-saving, less time-consuming cutting operations. Accordingly, there is a tendency that the condition of the cutting operation has changed to the severe side, such as high speed, along with the improvement of the performance of a cutting machine. With regard to various kinds of coated cutting tools conventionally proposed, as far as they are used in cutting operations of steel or cast iron using the usual cutting conditions, it has almost no problem. However, when they are used in high speed cutting operations, the hardness of these tools, especially at cutting edges, falls remarkably due to the extremely high heat generated. Therefore, thermal plastic deformation along the edge line occurs, and it promotes the severe wear of the cutting edge. As a result, the tool life becomes comparatively short.

SUMMARY OF THE INVENTION

[0011] Accordingly, the object of this invention provides for a coated cutting tool which has excellent strength and hardness at high temperatures and resists thermal plastic deformation at its cutting edge for a long period of time even when the machining process is performed under the severe conditions such as high speed cutting operations of, for example, steels and cast irons which conditions are accompanied by a high heat evolution.

[0012] The object of the present invention has been satisfied by the discovery of a coated cutting tool whose hard sintered substrate is coated with a hard coating layer preferably comprising an inner hard layer deposited by physical vapor deposition and has residual compressive stress, and an outer Al2O3 layer deposited by chemical vapor deposition at a middle temperature, for example, 700-850° C. This coated cutting tool gives excellent wear resistance even at the high speed cutting operations and enables the prolongation of tool life. Thus, they can respond sufficiently satisfactorily to the labor-saving and energy-saving of the cutting operations.

BRIEF DESCRIPTION OF THE DRAWINGS

[0013] A more complete appreciation of the invention and many of the attendant advantages thereof will be readily obtained as the same becomes better understood by reference to the following detailed description when considered in connection with the accompanying drawings, wherein:

[0014]
FIG. 1 shows an explanatory drawing of the arc ion plating equipment;

[0015]
FIG. 2 shows a perspective diagram of a coated insert (a), and a cross-sectional view of the coated insert (b);

[0016]
FIG. 3 shows a side view of a coated end mill (a), and a cross-sectional view of the coated end mill (b); and

[0017]
FIG. 4 shows a side view of a coated drill (a), and a cross-sectional view of the coated drill (b).

DESCRIPTION OF THE PREFERRED EMBODIMENTS

[0018] Reference is now made to the drawings, wherein like reference numerals designate identical or corresponding parts throughout the several views.

[0019] The present invention provides for a coated cutting tool having a cutting tool member that is coated with a hard coating layer. A “cutting tool member” refers to the part of the cutting tool that actually cuts the work piece. Cutting tool members include exchangeable cutting inserts to be mounted on bit holders of turning tools, face milling cutter bodies, and end-milling cutter bodies. They also include a cutting blade of drills and end mills. The cutting tool member is preferably made of a hard sintered substrate such as tungsten carbide-based cemented carbide.

[0020] A hard coating layer coats preferably a part of the surface, more preferably the entire surface of the cutting tool member. The hard coating layer is preferably made of an inner hard layer deposited by physical vapor deposition and has residual compressive stress, and an outer Al2O3 layer deposited by chemical vapor deposition at a middle temperature, for example, 700-850° C.

[0021] The preferred embodiments of the present invention were discovered after testing many different kinds of hard coating layers on hard sintered substrates such as cemented carbide, from the standpoint of developing a novel long lifetime coated cutting tool, which has high strength and high hardness even at high temperature. From these tests, the following results (A) to (C) were found:

[0022] (A) Although the hard coating layer such as a TiN layer or a (Ti, Al) N layer having a compressive stress deposited by physical vapor deposition has an excellent high temperature strength, it cannot maintain sufficient high temperature hardness if it is used at high speed cutting operations because the cutting edge is exposed to severe heat.

[0023] (B) A coated cutting tool with a hard coating layer has the above-mentioned hard inner layer having compressive stress deposited by physical vapor deposition, and an aluminum oxide (hereinafter referred to as Al2O3) outer layer deposited on said inner layer by chemical vapor deposition, and demonstrates high wear resistance and long tool life even when it is applied to a high speed cutting operation, because the above-mentioned Al2O3 has excellent high temperature hardness, then the hard coating layer consisting of a laminating layer could have both excellent high temperature strength and excellent high temperature hardness to inhibit excessive wear.

[0024] (C) When the Al2O3 layer which has mainly a κ-type crystal structure (hereinafter referred to as κ-Al2O3) is formed by chemical vapor deposition at a middle temperature such as 750-850° C., the produced κ-Al2O3 layer has extremely high hardness at high temperature, so the hard coating layer which has the above-mentioned κ-Al2O3 layer as an outer layer possesses further excellent high temperature strength and hardness. Therefore, the coated cutting tool having this structure has a superior cutting performance.

[0025] Based on these results, the present invention provides for a coated cutting tool which is formed by the hard coating layers consisting of the following features (a) and (b), and can demonstrate excellent wear resistance even in high-speed cutting:

[0026] (a) The hard coating layer, as the inner layer, having an average thickness of 0.5-10 μm and residual compressive stress; and

[0027] (b) the Al2O3 layer, as the outer layer, having an average thickness of 0.1-5 μm, and being formed by chemical vapor deposition at a middle temperature.

[0028] The reason for limiting the average thickness of the above-mentioned inner layer of the hard coating layer to 0.1-10 μm is the following: When the average thickness is less than desired, high wear resistance cannot be given to the hard coating layer, so that the wear progress on the cutting edge is severe. On the other hand, when the average thickness is more than 10 μm, it becomes easy to cause chipping at the cutting edge. However, in the tools with comparatively high strength for the cutting edge such as an insert, it is preferable to limit the average thickness to 0.5-10 μm; on the other hand, in the tools where the cutting edges receive especially severe impacts, like an end mill, it is preferable to limit the average thickness to 0.1-3 μm.

[0029] Moreover, the reason for limiting the average thickness of the Al2O3 layer composing the outer layer to 0.1-5 μm is following: When the thickness is less than 0.1 μm, the desired hardness at high temperature cannot be given to the hard coating layer, so that the desired enhancement effect to the wear resistance of the cutting edge is not obtained. On the other hand, when the thickness is more than 5 μm, it becomes easy to cause breaking or chipping at the cutting edge. However, in the tools where the cutting edges receive especially severe impacts, like an end mill, it is preferable to limit the average thickness to 0.1-3 μm.

EXAMPLES

[0030] Having generally described this invention, a further understanding can be obtained by reference to certain specific examples which are provided herein for purposes of illustration only and are not intended to be limiting unless otherwise specified.

Example 1

[0031] As a raw material powder, middle coarse grain WC powder having 5.5 μm for the average particle diameter, fine WC powder having 2.3 μm for the average particle diameter, TaC powder having 1.3 μm for the average particle diameter, TiC powder having 1.3 μm for the average particle diameter, TaC powder having 1.3 μm for the average particle diameter, NbC powder having 1.2 μm for the average particle diameter, (Ta, Nb)C (it is TaC/NbC=50/50 by mass ratio) powder having 1.0 μm for the average particle diameter, (Ti, W)C (it is TiC/WC=70/30 by mass ratio) powder having 1.0 μm for the average particle diameter, Ca powder having 1.8 μm for the average particle diameter, are prepared, and these raw material powders are blended with the formulation composition shown in Table 1 respectively.

[0032] Furthermore, a wax is added and mixed in acetone for 24 hours by ball milling, and after milling, the mixed powder was dried under a reduced pressure and pressed to the green compact of a predetermined configuration by 1 MPa. Further, these green compacts are heated up to the predetermined temperature in the range of 1370 to 1470° C. by a programming rate of 7° C./minute, under 6 Pa of vacuum, and kept for 1 hour to perform sintering. After that, they are cooled in the condition of a furnace cooling, and further, the honing of R:0.05 is given to the part of the cutting edge. Then the substrates made from the WC base cemented carbide A1˜A12 having CNMG120408 for the insert configuration of an ISO specification, were made respectively.

[0033] Next, these substrates A1-A12 are cleaned ultrasonically in acetone, and charged respectively into the conventional arc ion plating equipment shown in FIG. 1. On the other hand, the Ti-Al alloys having venous compositions are set as the cathode electrode (evaporation source), and the inside of the equipment is evacuated to keep 0.5 Pa and heated to 500° C. by the heater. Then, Ar is introduced in the equipment to 10 Pa. The bias potential of −800 V is applied to the substrate in this state, and the surface of the substrate is cleaned by Ar bombardment. Next, while introducing nitrogen gas as reaction gas in the system and setting to 6 Pa of reaction pressure, the bias potential applied to the above-mentioned substrate is lowered to −200 V, and the arc discharge is generated between the above-mentioned cathode electrode and the anode electrode. Then, the designated composition (X value) with the thickness of the (Ti, Al) N layer, which are shown in Table 2, is formed as the inner layer of the hard coating layer.

[0034] Furthermore, the κ-Al2O3 layer with the designated thickness shown in Table 2 similarly, is formed as the outer layer on the surface of the above-mentioned inner layer, by using the conventional chemical vapor deposition equipment in the following conditions.

[0035] The reaction gas composition is set to the conventional reaction gas composition, i.e.,

[0036] AlCl3 is 2% by volume,

[0037] CO2 is 3% by volume,

[0038] H2S is 0.3% by volume,

[0039] HCl is 1% by volume, and

[0040] H2 is residual.

[0041] The reaction pressure is also the same value as the conventional condition, i.e., 7 KPa, but the reaction temperature is set to the middle temperature for chemical vapor deposition conditions, i.e., the reaction temperature is 800° C., which is considerably lower in comparison with 1000-1050° C. for the conventional reaction temperature. Then, the coated and cemented carbide inserts 1 to 12 of this invention were made respectively, in which their structures are shown in FIG. 2(a) as the rough perspective view and in FIG. 2(b) as the rough cross sectional view.

[0042] Moreover, for the comparative objective, the conventional coated and cemented carbide inserts 1-12 were made, which consist only of the (Ti, Al)N-layer as the inner layer in the same conditions, excepting to form the κ-Al2O3 layer by the above-mentioned middle temperature chemical vapor deposition, as shown in Table 3.

[0043] In addition, for the hard coating layers of the coated and cemented carbide inserts 1-12 of this invention and the conventional coated and cemented carbide inserts 1-12, the compositions of the center area in the thickness direction of the inner layers were measured by using Auger Electron Spectral analysis equipment, and cross sectional measurements of the thickness were done by using a scanning electron microscope. Then, both of them were indicated with the same values substantially as the designated composition and thickness.

[0044] Next, for the above-mentioned coated and cemented carbide inserts of this invention 1-12 and the conventional coated and cemented carbide inserts 1-12, the cutting performance tests were done by screw setting these inserts at the top of the bite holder made of a tool steel.

[0045] (1-1) Cutting style: High-speed continuous turning of alloyed steel

[0046] Work material: Round bar of JIS-SCM440

[0047] Cutting speed: 375 m/min.

[0048] Depth of cut: 1.5 mm.

[0049] Feed rate: 0.2 mm/rev.

[0050] Cutting time: 5 min.

[0051] Coolant: Dry

[0052] (1-2) Cutting style: High-speed continuous turning of cast iron

[0053] Work material: Round bar of JIS-FC250

[0054] Cutting speed: 405 m/min.

[0055] Depth of cut: 1.5 mm.

[0056] Feed rate: 0.3 mm/rev.

[0057] Cutting time: 10 min.

[0058] Coolant: Dry

[0059] The flank wear of the cutting edge was measured in both tests. These measurement results are shown in Tables 2 and 3, respectively.

Example 2

[0060] As a raw material powder, middle grain WC powder having 3.0 μm for the average particle diameter, TiC powder having 1.5 μm for the average particle diameter, (Ti, W)C (TiC/WC=70/30 by mass ratio) powder having 1.0 μm for the average particle diameter, (Ta, Nb)C (TaC/NbC=50/50 by mass ratio) powder having 1.0 μm for the average particle diameter, Co powder having 1.8 μm for the average particle diameter, were prepared, and these raw material powders were blended with the composition shown in Table 4 respectively. Furthermore, the wax was added and mixed in acetone for 24 hours by ball milling, and after mixing, the mixed powder was dried under the reduced pressure and pressed to the green compact of the predetermined configuration by 1 MPa. After that, these green compacts were sintered and were heated up to a predetermined temperature in the range of 1370 to 1470° C. by a programming rate of 7° C./minute, under 6 Pa of vacuum, kept for 1 hour, and cooled in the furnace. After sintering, the honing of R:0.05 was given to the part of the cutting edge. Then the substrates made with WC-based cemented carbide A13˜A18 having CNMG120408 as the insert configuration of an ISO specification, were made respectively.

[0061] Moreover, TiCN (TiC/TiN=50/50 by weight ratio) powder, Mo2C powder, ZrC powder, NbC powder, TaC powder, WC powder, Co powder, and Ni powder, were used as the raw material powder, in which all of said powders have {fraction (0/5)}-2 μm for the average grain size, and these raw material powders were blended with the compositions shown in Table 5. Wet blending was done by ball milling for 24 hours, and after drying, press forming was done to the green compact by the pressure of 100 MPa. After that, this green compact was sintered for 1 hour by keeping it at the temperature of 1500° C. under 2 kPa of nitrogen atmosphere. Furthermore, after sintering, the honing of R0.05 was given to the part of the cutting edge. Then, the substrates B1-B6 made with TiCN base cermets having CNMG120408 as the insert configuration of an ISO specification were made respectively.

[0062] Next, these substrate A13-18 and B1-B6 were washed by ultrasonic waves in acetone, and were charged respectively in the conventional arc ion plating equipment shown in FIG. 1, after being dried. Then, the hard coatings, in which various residual compression stresses were given, were deposited as the inner layer on the surface of the substrates A13 to A18 and B1 to B6, to which bias potential was applied by generating the arc discharge between the evaporation source (cathode electrode) having the various compositions shown in Table 7 and the anode electrode, in the same method as Example 1. Furthermore, Al2O3 layers having the designated thickness shown in Table 7 were coated on the above-mentioned inner layers as the outer layers were under the conditions shown in Table 6 by using the conventional chemical vapor deposition equipment. Then, the coated and cemented carbide inserts of this invention were made, and the structures of these coated and cemented carbide inserts are shown in FIG. 2(a) which is the rough perspective view and in FIG. 2(b) which is the rough cross-sectional view. These views are the same as Example 1.

[0063] Moreover, for the comparative objective, the conventional coated and cemented carbide inserts 13-24, in which the hard coating layer comprised only the inner layer, were made respectively under the same conditions excepting the formation of Al2O3 layers by the above-mentioned middle temperature chemical-vapor-deposition process, as shown in Table 8.

[0064] In addition, for the hard coating layer of coated and cemented carbide inserts of this invention 13 to 24 and the conventional coated and cemented carbide inserts 13 to 24, the compositions of the center area in the thickness direction of the inner layers were measured by using Auger Electron Spectral analysis equipment, and cross-sectional measurements of the thickness were done by using the scanning electron microscope. Then, both of them were indicated as having the same values substantially as the designated composition and thickness.

[0065] Next, for the above-mentioned coated and cemented carbide inserts of this invention 13 to 24 and the conventional coated and cemented carbide inserts 13 to 24, the cutting performance tests were done under the following conditions by screw setting these inserts at the top of the bite holder made with a tool steel.

[0066] (2-1) Cutting style: High-speed continuous turning of alloyed steel

[0067] Work material: Round bar of JIS-SCM440

[0068] Cutting speed: 400 m/min.

[0069] Depth of cut: 1.5 mm.

[0070] Feed rate: 0.2 mm/rev.

[0071] Cutting time: 3 min.

[0072] Coolant: Dry

[0073] (2-2) Cutting style: High-speed continuous turning of cast iron

[0074] Work material: round bar of JIS-FC250

[0075] Cutting speed: 450 m/min.,

[0076] Depth of cut: 1.5 mm,

[0077] Feed rate: 0.3 mm/rev.,

[0078] Cutting time: 5 minutes.

[0079] These measurement results are shown in Tables 7 and 8, respectively.

Example 3

[0080] As the raw material powder, Coarse grain WC powder having 5.5 μm for the average particle diameter, Granular WC powder having 0.8 μm for the average particle diameter, Cr3C2 powder having 2.3 μm for the average particle diameter, VC powder having 1.2 μm for the average particle diameter, TIC powder having 1.5 μm for the average particle diameter, TaC powder having 1.3 μm for the average particle diameter, NbC powder having 1.2 μm for the average particle diameter, (Ta, Nb)C [TaC/NbC=50/50 by mass ratio] powder having 1.0 μm for the average particle diameter, (Ti, W)C [TiC/WC=70/30 by mass ratio] powder having 1.0 μm for the average particle diameter, and Co powder having 1.8 μm for the average particle diameter, were prepared and these raw material powders were blended with the composition shown in Table 9, respectively. Furthermore, wax was added and mixed in acetone for 24 hours by ball milling, and after mixing, the mixed powder was dried under the reduced pressure and pressed to the green compact of the predetermined configuration by 100 MPa. After that, these green compacts were sintered and heated up to the predetermined temperature in the range of 1370 to 1470° C. by a programming rate of 7° C./minute, under 6 Pa of vacuum, kept for 1 hour, and cooled in the furnace. Then, three sorts of round bar cemented carbide bodies were formed, in which the diameters were 8 mm, 13 mm, and 26 mm. Furthermore, the cemented-carbide end mills a to 1 were made respectively from the above-mentioned three sorts of round-bar bodies by the grinding process in which the dimensions of diameter×length of the cutting edge are φ6 mm×13 mm, φ10 mm×22 mm, and φ20 mm×45 mm shown in Table 9.

[0081] Next, honing was done to these cemented-carbide end mills a to 1, and these end mills were washed by ultrasonic waves in acetone, and were charged respectively in the conventional arc ion plating equipment shown in FIG. 1, after being dried. Moreover, (Ti, Al)N layers of the objective composition (X value) and the objective thickness shown in Table X, were deposited as the inner layer of the hard coating layer on each surface of the cemented-carbide end mill a to 1 to which bias potential was applied by generating the arc discharge between the cathode electrode (evaporation source) equipped with the Ti-Al alloy having the various compositions, and anode electrodes, in the same method as example 1. Furthermore, the κ-Al2O3 layer having the objective thickness shown in Table 9 was coated on the above-mentioned inner layer as the outer layer by using the conventional chemical vapor deposition equipment. Then, the coated end mills of this invention 1-12 were made respectively, and the structure of these end mills is shown in FIG. 3(a) as a side view and in FIG. 3(b) as a cross-sectional view.

[0082] Moreover, for the comparative objective, the conventional coated end mills 1 to 12, in which the hard coating layer comprised only a (Ti, Al) N layer which is the inner layer, were made respectively under the same conditions excepting the formation of the κ-Al2O3 layer by the above-mentioned middle temperature chemical vapor deposition process, as shown in Table 11. In addition, for the coating layer of the coated end mills 1 to 12 of this invention and the conventional coated end mills 1 to 12, the compositions of the center area in the thickness direction of the individual layers were measured by using Auger Electron Spectral analysis equipment, and cross-sectional measurements of the thickness were done by using the scanning electron microscope. Then, both of them were indicated with the same values substantially as the designated composition and thickness.

[0083] Next, for the coated end mills of this invention 1 to 4 and the conventional coated end mills 1 to 4, the cutting performance tests were done under the following conditions:

[0084] (3-1) Cutting style: High-speed groove milling on alloyed steel

[0085] Work material: 100 mm×250 mm, thickness: 50 mm, JIS-NAK

[0086] square plate

[0087] Rotational speed: 7000 r.p.m.

[0088] Depth of cut: 3 mm

[0089] Table feed rate: 500 mm/min.

[0090] Coolant: Water-soluble coolant.

[0091] For the coated end mills of this invention 5 to 8 and the conventional coated end mills 5 to 8, the cutting performance tests were done under the following conditions:

[0092] (3-2) Cutting style: High-speed groove milling on alloyed steel

[0093] Work material: 100 mm×250 mm, thickness: 50 mm, JIS-SCM 440

[0094] square plate

[0095] Rotational speed: 6000 r.p.m.

[0096] Depth of cut: 5 mm

[0097] Table feed rate: 700 mm/min.

[0098] Coolant: Water-soluble coolant.

[0099] For the coated end mills of this invention 9 to 12 and the coated end mills of the conventional 9 to 12, the cutting performance tests were done under the following conditions:

[0100] (3-3) Cutting style: High-speed groove milling on cast iron

[0101] Work material: 100 mm×250 mm, thickness: 50 mm, JIS-FC250

[0102] square plate

[0103] Rotational speed: 5000 r.p.m.

[0104] Depth of cut: 10 mm

[0105] Table feed rate: 3000 mm/min.

[0106] Coolant: Water-soluble coolant.

[0107] In all wet high-speed groove cutting tests, the cut length was measured; when the nose diameter of the cutting edge reduces by 0.2 mm, this is the end of the usual tool life. These measurement results are shown in Tables 10 and 11, respectively.

Example 4

[0108] As the raw material powder, Coarse grain WC powder having 5.5 μm for average particle diameter, granular WC powder having 0.5 mm for average particle diameter, Cr3C2 powder having 2.3 μm for average particle diameter, TiC powder having 1.5 μm for average particle diameter, TaC powder having 1.3 μm for average particle diameter, NbC powder having 10 μm for average particle diameter, (Ta, Nb)C [TaC/NbC=50/50 by mass ratio] powder having 1.0 μm for average particle diameter, (Ti, W) C[TiC/WC=70/30 by mass ratio] powder having 1.0 μm for average particle diameter, and Co powder having 1.8 μm for average particle diameter, were prepared and these raw material powders were blended with the composition shown in Table 12, respectively. Furthermore, wax was added and mixed in acetone for 24 hours by ball milling, and after mixing, the mixed powder was dried under the reduced pressure and pressed into the green compact of the predetermined configuration by 100 MPa. After that, these green compacts were sintered in a process in which they were heated up to the predetermined temperature in the range of 1370-1470° C. by a programming rate of 7° C./minute, under 6 Pa vacuum, kept for 1 hour, and cooled in the furnace. Then, three sorts of round bar sintered bodies were formed with the diameters being 8 mm, 13 mm, and 26 mm, respectively. Furthermore, cemented carbide drills a′ to 1′ were made respectively from three sorts of the above-mentioned round-bar bodies by the grinding process in which the diameter×length of the edge formation section is φ6 mm×13 mm, φ10 mm×22 mm, and φ20 mm×45 mm, respectively shown in Table 7.

[0109] Next, honing was done to these cemented carbide drills a′ to 1′. These drills were then washed by ultrasonic waves in acetone and were charged respectively in the conventional arc ion plating equipment shown in FIG. 1, after being dried. Moreover, (Ti, Al)N layers of the objective composition (X value) with the objective thickness were deposited as the inner layer on the surface of the cemented carbide drills a′ to 1′ to which bias voltage was applied by generating the arc discharge between the cathode electrode (evaporation source) equipped with the Ti-Al alloy having the various compositions and the anode electrode, in the same method as example 1. Furthermore, the κ-Al2O3 layer having the objective thickness shown in Table 12, was coated on the above-mentioned inner layer as the outer layer by using conventional chemical vapor deposition equipment. Then, the coated drills of this invention were made respectively. The structure of these drills is shown in FIG. 4(a) which is the side view and in FIG. 4(b) which is the cross-sectional view.

[0110] Moreover, for the comparative objective, the conventional coated drills 1-12, in which the hard coating layer comprised only the (Ti, Al)N layer which is the inner layer, were made respectively under the same conditions excepting the formation of the κ-Al2O3 layer, by the above-mentioned middle temperature chemical vapor deposition process, as shown in Table 14.

[0111] In addition, for the hard coating layer of the coated drills of this invention 1-12 and the coated drills of conventional 1-12, the compositions of the center area in the thickness direction of the individual layers were measured by using Auger Electron Spectral analysis equipment and cross-sectional measurements of the thickness were done by using the scanning electron microscope. Then, both of them were indicated with the same values substantially as the designated composition and thickness.

[0112] Next, for the coated drills of this invention 1 to 4 and the coated drills of conventional 1 to 4, the cutting performance tests were done under the following conditions:

[0113] (4- 1) Cutting style: Drilling on alloyed steel

[0114] Work material: 100 mm×250 mm, thickness: 50 mm, JIS-SCM440

[0115] square plate

[0116] Rotational speed: 1000 r.p.m.

[0117] Feed rate: 4.25 mm/rev.

[0118] Coolant: Water-soluble coolant.

[0119] For the coated drills of this invention 5 to 8 and the coated drills of conventional 5 to 8, the cutting performance tests were done under the following conditions:

[0120] (4-2) Cutting style: Drilling on cast iron

[0121] Work material: 100 mm×250 mm, thickness: 50 mm, JIS-FC200

[0122] square plate

[0123] Rotational speed: 7500 r.p.m.

[0124] Feed rate: 0.30 mm/rev.

[0125] Coolant: Water-soluble coolant.

[0126] For the coated drills of this invention 9 to 12 and the coated drills of conventional 9 to 12, the cutting performance tests were done under the following conditions:

[0127] (4-3) Cutting style: Drilling on alloyed steel

[0128] Work material: 100 mm×250 mm, thickness: 50 mm, JIS-SCM440

[0129] square plate

[0130] Rotational speed: 3500 r.p.m.

[0131] Feed rate: 0.35 mm/rev.

[0132] Coolant: Water-soluble coolant.

[0133] In all wet high-speed drilling tests, the numbers of drilled holes were measured when the flank wear width of the cutting edge came down to 0.3 mm. These measurement results are shown in Tables 13 and 14, respectively.

[0134] Obviously, numerous modifications and variations of the present invention are possible in light of the above teachings. It is therefore to be understood that, within the scope of the appended claims, the invention may be practiced otherwise than as specifically described herein.

1TABLE 1CarbideComposition (wt %)substrate(Ta,(Ti,for insertCoCr3C2TiCTaCNbCNb)CW)CWCA110 0.7—————Fine:BalanceA212 1—————Fine:BalanceA350.3—————Fine:BalanceA460.1———1—Fine:BalanceA580.7—1———Fine:BalanceA650.1444——Coarse:BalanceA760.25——55Coarse:BalanceA870.3691—3Coarse:BalanceA980.512 5—6—Coarse:Balance A1090.1———12 8Coarse:Balance A1110 15——510 Coarse:Balance A1212 27 4.5 4.518Coarse:Balance

[0135]

2

TABLE 2

Hard coating layer

Outer

layer
Flank wear at

Inner layer (Ti1−xAlx)N
(κ-Al203)
continuous

designed
designed
designed
turning (mm)

Sub-
X value
thickness
thickness
alloyed
cast

Insert
strate
(atomic ratio)
μm)
(μm)
steel
iron

This in-

vention

1
A1
0.2
5
2
0.24
0.18

2
A2
0.5
10
5
0.22
0.19

3
A3
0.4
3
4
0.23
0.20

4
A4
0.3
7
2
0.20
0.21

5
A5
0.4
7
3
0.26
0.22

6
A6
0.5
0.5
5
0.28
0.18

7
A7
0.5
10
0.1
0.21
0.28

8
A8
0.6
6
4
0.20
0.22

9
A9
0.4
3
2
0.21
0.24

10
A10
0.5
5
2
0.23
0.25

11
A11
0.2
4
5
0.25
0.19

12
A12
0.5
8
4
0.24
0.22

[0136]

3

TABLE 3

Hard coating layer

Inner layer

(Ti1−xAlx)N
Outer layer
Flank wear at

designed

(κ-Al203)
continuous

X value
designed
designed
turning (mm)

Sub-
(atomic
thickness
thickness
alloyed
cast

Insert
strate
ratio)
(μm)
(μm)
steel
iron

Con-

ventional

1
A1
0.2
5
—
0.75
0.72

2
A2
0.5
10
—
0.58
0.59

3
A3
0.4
3
—
0.84
0.84

4
A4
0.3
7
—
0.66
0.60

5
A5
0.4
7
—
0.65
0.61

6
A6
0.5
0.5
—
1.15
1.21

7
A7
0.5
10
—
0.55
0.57

8
A8
0.6
6
—
0.68
0.72

9
A9
0.4
3
—
0.83
0.89

10
A10
0.5
5
—
0.75
0.78

11
A11
0.2
4
—
0.80
0.84

12
A12
0.5
8
—
0.61
0.65

[0137]

4

TABLE 4

Carbide substrate for
Composition (wt %)

insert
Co
TiC
(Ti, W)C
(Ta, Nb)C
WC

A13
6
—
—
1.5
Balance

A14
6
—
8.5
3
Balance

A15
7
3.5
5.5
4
Balance

A16
8
4
4
5
Balance

A17
9
21
—
2
Balance

A18
10
—
—
2
Balance

[0138]

5

TABLE 5

Carbide

substrate
Composition (wt %)

for insert
Co
Ni
ZrC
TaC
NbC
Mo2C
WC
TiCN

B1
13
5
—
10
—
10
16
Balance

B2
8
1
—
5
—
7.5
—
Balance

B3
5
—
—
—
—
6
10
Balance

B4
10
5
—
11
2
—
—
Balance

B5
9
4
1
8
—
10
10
Balance

B6
12
5.5
—
10
—
9.5
14.5
Balance

[0139]

6

TABLE 6

Coating Condition

Ambience

Composition of reactive
Pressure
Temperature

Hard Coating Layer
gas (volume %)
K(Pa)
(° C.)

κ-Al2O3 {circle over (1)}
AlCl3: 2%, CO2: 3%,
7
800

HCl: 1%, H2S: 0.3%,

H2: Residue

κ-Al2O3 {circle over (2)}
AlCl3: 2%, CO2: 2%,
7
750

HCl: 1.5%, H2S: 0.4%,

H2: Residue

α-Al2O3 {circle over (1)}
AlCl3: 1%, CO2: 10%,
7
850

HCl: 1%, H2S: 0.1%,

H2: Residue

α-Al2O3 {circle over (2)}
AlCl3: 1%, CO2: 15%,
7
850

HCl: 1.5%, H2S: 0.1%,

H2: Residue

[0140]

7

TABLE 7

Hard coating layer

(Figure in parenthesis

means designed thickness: μm)
Flank wear at

Inner layer

continuous

Target
turning (mm)

Sub-
com-

alloyed
cast

Insert
strate
position
Layer
Outer layer
steel
iron

This in-

vention

1
A13
Ti
TiN
κ-Al2O3 {circle over (1)}
0.22
0. 32

100%
(3.5)
(1)

2
A14
Ti
TiCN
κ-Al2O3 {circle over (1)}
0.25
0.35

100%
(5)
(2)

3
A15
Cr
CrN
κ-Al2O3 {circle over (1)}
0.27
0.30

100%
(7)
(2)

4
A16
Ti 50%/
(TiAl)CN
κ-Al2O3 {circle over (1)}
0.28
0.32

Al 30%
(3)
(0.5)

5
A17
Ti 60%/
(TiAl)N
κ-Al2O3 {circle over (1)}
0.30
0.33

Al 40%
(5)
(5)

6
A18
Ti 50%/
(TiZr)N
κ-Al2O3 {circle over (1)}
0.28
0.38

Zr 50%
(5)
(1)

7
B1
Ti 50%/
(TiV)N
κ-Al2O3 {circle over (2)}
0.31
0.30

V 50%
(10)
(2)

8
B2
Ti 50%/
(TiCr)N
κ-Al2O3 {circle over (2)}
0.25
0.38

Cr 50%
(4)
(1.5)

9
B3
Ti 50%/
(TiSi)N
κ-Al2O3 {circle over (2)}
0.24
0. 3R

Si 50%
(4)
(3)

10
B4
Ti 40%/
(TiAlZr)N
α-Al2O3 {circle over (1)}
0.29
0.35

Al 40%/
(5)
(2)

Zr 20%

11
B5
Ti 40%/
(TiAlV)N
α-Al2O3 {circle over (2)}
0.30
0.35

Al 40%/
(6)
(1)

V 20%

12
B6
Ti 40%/
(TiAlCr)N
α-Al2O3 {circle over (1)}
0.29
0.33

Al 40%/
(3)
(3)

Cr 20%

13
A1
Ti 40%/
(TiAlSi)N
α-Al2O3 {circle over (2)}
0.29
0.34

Al 40%/
(2)
(0.5)

Si 20%

14
A2
Ti 40%/
(TiAlY)N
α-Al2O3 {circle over (1)}
0.33
0.31

Al 40%/
(5)
(0.5)

Y 20%

15
A3
Ti 40%/
(TiAIY)CN
α-Al2O3 {circle over (2)}
0.28
0.32

Al 40%/
(5)
(1)

Y 20%

[0141]

8

TABLE 8

Hard coating layer

(Figure in parenthesis

means designed thickness: μm
Flank wear at

Inner layer

continuous

Target

turning (mm)

Sub-
com-

Outer
alloyed
cast

Insert
strate
position
Layer
layer
steel
iron

Conven-

tional

1
A13
Ti 100%
TiN (3.5)
—
0.77
0.92

2
A14
Ti 100%
TICN (5)
—
0.65
0.91

3
A15
Cr 100%
CrN (7)
—
0.64
0.76

4
A16
Ti 50%/
(TiAl)CN (3)
—
0.81
0.90

Al 50%

5
A17
Ti 60%/
(TiAl)N (5)
—
0.59
0.85

Al 40%

6
A18
Ti 50%/
(TiZr)N (5)
—
0.70
0.81

Zr 50%

7
B1
Ti 50%/
(TiV)N (10)
—
0.69
0.80

V 50%

8
B2
Ti 50%/
(TiCr)N (4)
—
0.80
0.86

Cr 50%

9
B3
Ti 50%/
(TiSi)N (4)
—
0.82
1.08

Si 50%

10
B4
Ti 40%/
(TiAlZr)N (5)
—
0.73
0.82

Al 40%/

Zr 20%

11
B5
Ti 40%/
(TiAlV)N (6)
—
0.74
0.79

Al 40%/

V 20%

12
B6
Ti 40%/
(TiAlCr)N (3)
—
0.62
1.01

Al 40%/

Cr 20%

13
A1
Ti 40%/
(TIAlSi)N (2)
—
0.64
0.95

Al 40%/

Si 20%

14
A2
Ti 40%/
(TiAlY)N (5)
—
0.70
0.95

Al 40%/

Y 20%

15
A3
Ti 40%/
(TiAlY)CN (5)
—
0.63
0.93

Al 40%/

Y 20%

[0142]

9

TABLE 9

Carbide

Size

substrate for
Composition (wt %)
(diameter ×

End-mill
Ca
Cr3C2
VC
TiC
TaC
NbC
(Ta,Nb)C
(Ti,W)C
WC
length: mm)

a
15
0.5
2
—
—
—
—
—
Fine: Balance
φ6 × 13

b
8
0.4
0.3
—
—
—
—
—
Fine: Balance
φ6 × 13

c
9
0.1
0.1
9
—
—
12
—
Coarse: Balance
φ6 × 13

d
15
2
2
—
9
1
—
13
Coarse: Balance
φ6 × 13

e
10
0.5
0.4
—
—
—
—
—
Fine: Balance
φ10 × 22

f
10
0.7
0.5
—
—
—
—
—
Fine: Balance
φ10 × 22

g
12
0.6
0.4
—
2
—
2
2
Fine: Balance
φ10 × 22

h
13
0.1
0.1
—
—
—
10
10
Coarse: Balance
φ10 × 22

i
7
0.3
0.2
—
—
—
—
—
Fine: Balance
φ20 × 45

j
5
0.2
0.1
—
—
—
—
—
Fine: Balance
φ20 × 45

k
5
0.1
0.1
3
2
1
—
—
Coarse: Balance
φ20 × 45

l
8
0.4
0.3
7
4.5
0.5
5
1
Coarse: Balance
φ20 × 45

[0143]

10

TABLE 10

Hard coating layer

Inner layer

(Ti1−xAlx)N
Outer layer

designed

(κ-Al2O3)

X value
designed
designed
Cutting

Sub-
(atomic
thickness
thickness (μm)
length

End-mill
strate
ratio)
(μm)
(μm)
(m)

This in-

vention

1
a
0.2
3
0.1
352

2
b
0.5
2
0.5
500

3
c
0.6
1.5
1
422

4
d
0.4
1
1
404

5
e
0.6
0.1
3
206

6
f
0.5
1
2
478

7
g
0.3
2
1
452

8
h
0.6
3
0.5
480

9
1
0.6
2
0.5
512

10
j
0.5
1.5
1
497

11
k
0.5
1.5
1
500

12
1
0.6
2
1
515

[0144]

11

TABLE 11

Hard coating layer

Inner layer (Ti1-xAlx)N
Outer layer (κ-A1203)

designed X value
designed thickness

Cutting length

End-mill
Substrate
(atomic ratio)
(μm)
designed thickness (μm)
(m)

Conven-
1
a
0.2
3
—
82

tional
2
b
0.5
2
—
78

3
c
0.6
1.5
—
70

4
d
0.4
1
—
72

5
e
0.6
0.1
—
48

6
f
0.5
1
—
62

7
g
0.3
2
—
81

8
h
0.6
3
—
92

9
i
0.6
2
—
83

10
j
0.5
1.5
—
77

11
k
0.5
1.5
—
64

12
l
0.6
2
—
69

[0145]

12

TABLE 12

Carbide

Size

substrate far
Composition (wt %)
diameter ×

drill
Co
Cr3C2
TiC
TaC
NbC
(Ta,Nb)C
(Ti,W)C
WC
length: mm)

a′
15
2
—
—
—
—
—
Fine: Balance
φ6 × 13

b′
10
0.7
—
—
—
—
—
Fine: Balance
φ6 × 13

c′
9
0.1
8
—
—
12
—
Coarse: Balance
φ6 × 13

d′
15
1.5
—
9
1
—
15
Coarse: Balance
φ6 × 13

e′
12
1
—
—
—
—
—
Fine: Balance
φ10 × 22

f′
10.5
0.8
—
—
—
—
—
Fine: Balance
φ10 × 22

g′
14
1.5
—
3
—
2
—
Fine: Balance
φ10 × 22

h′
10
0.1
—
—
—
12
12
Coarse: Balance
φ20 × 22

i′
5
0.1
—
—
—
—
—
Fine: Balance
φ20 × 45

j′
7
0.5
—
—
—
—
—
Fine: Balance
φ20 × 45

k′
7
0.2
4
4
4
—
—
Coarse: Balance
φ20 × 45

l′
10
0.1
8
4.5
0.5
7
5
Coarse: Balance
φ20 × 45

[0146]

13

TABLE 13

Hard coating layer

Inner layer (Ti1-xAlx)N
Outer layer (κ-A1203)

designed X value
designed thickness
designed thickness

Drill
Substrate
(atomic ratio)
(μm)
(μm)
Number of holes

This
1
a′
0.2
0.5
4
2000

invention
2
b′
0.5
3
2
2550

3
c′
0.4
2
2
2400

4
d′
0.6
4
0.5
2100

5
e′
0.3
6
2
2350

6
f′
0.5
10
5
3000

7
g′
0.6
7
1
2400

8
h′
0.2
7
2
2550

9
i′
0.6
10
3
2950

10
j′
0.5
8
4
2800

11
k′
0.4
9
3
2800

12
l′
0.3
7
5
2400

[0147]

14

TABLE 14

Hard coating layer

Inner layer (Ti1-xAlx)N
Outer layer (κ-A1203)

designed X value
designed thickness
designed thickness

Drill
Substrate
(atomic ratio)
(μ)
(μ)
Number of holes

Conven-
1
a′
0.2
0.5
—
280

tional
2
b′
0.5
3
—
550

3
c′
0.4
2
—
450

4
d′
0.6
4
—
600

5
e′
0.3
6
—
400

6
f′
0.5
10
—
600

7
g′
0.6
7
—
550

8
h′
0.2
7
—
500

9
i′
0.6
10
—
500

10
j′
0.5
8
—
700

11
k′
0.4
9
—
650

12
l′
0.3
7
—
650

Number	Date	Country
2000-390038	Dec 2000	JP
2000-390039	Dec 2000	JP
2000-390040	Dec 2000	JP
2001-054097	Feb 2001	JP
2001-054098	Feb 2001	JP

Coated cutting tool

Information

Publication Number

Date Filed

Date Published

Inventors

Original Assignees

CPC

US Classifications

International Classifications

Abstract

Description

Claims

Priority Claims (5)