USPatent applicationPatented

Nanolaminated coated cutting tool

Granted 21 Oct 2014 · 1 office action

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Abstract

A cutting tool insert for machining by chip removal includes a body of polycrystalline cubic boron nitride compact (PCBN), either as a solid insert or attached to a backing body, onto which a hard and wear resistant PVD coating is deposited. The coating includes a polycrystalline nanolaminated structure of alternating A and B layers, where layer A is (Ti,Al,Me1)N and Me1 is one or more of the metal elements from group 3, 4, 5 or 6 in the periodic table, layer B is (Ti,Si,Me2)N and Me2 is one or more of the metal elements from group 3, 4, 5 or 6 in the periodic table including Al with a thickness between 0.5 and 10 μm. The insert is particularly useful in metal cutting applications generating high temperatures, e.g., high speed machining of steels, cast irons, super alloys and hardened steels.

Description

9 parts
›BACKGROUND OF THE INVENTION

The present invention relates to a cutting tool insert comprising a body of cubic boron nitride compact (PCBN) material and a hard and wear resistant coating comprising a nanolaminated structure based on (Ti,Al)N and (Ti,Si)N layers, respectively. This insert is particularly useful in metal cutting applications generating high temperatures, e.g., high speed machining of steels, cast irons, super alloys, stainless steels and hardened steels. The coating is grown by physical vapour deposition (PVD) and preferably by cathodic arc evaporation.

U.S. Pat. No. 7,056,602 discloses a cutting tool insert coated with a cubic structured (Ti y Al x Me 1-x-y )N based layer where Me is one of the elements: Zr, Hf, V, Nb, Ta, Cr, Mo, W or Si, and: x is between 0.50 and 0.80; the ratio, x/(x+y), is between 0.50 and 0.85; the sum of the Ti and Al subscripts, x+y, is between 0.7 and 1.0.

EP 1736565 discloses a cutting tool cubic boron nitride based insert coated with a cubic structured (Me,Si)X phase, where Me is one or more of the elements Ti, V, Cr, Zr, Nb, Mo, Hf, Ta and Al, and X is one or more of the elements N, C, O or B.

EP 0588350 discloses a hard layer of Ti—Si—N composite material on a body, the layer being deposited using a source of evaporation possessing a composition of Ti a Si b with a in the range of 75-85 at % and b 15-25 at %.

Coating optimization has also been obtained by applying different concepts of multilayers as; alternating Ti and Al containing layers (U.S. Pat. No. 6,309,738), oxygen and non-oxygen containing layers (U.S. Pat. No. 6,254,984), one of the layers stacked in the multilayer consists itself of a multilayer (U.S. Pat. No. 6,077,596), alternating nitrogen content (U.S. Pat. No. 5,330,853) or using one metastable compound (U.S. Pat. No. 5,503,912) or as aperiodic multilayer (U.S. Pat. No. 6,103,357).

Further improvements in thermal stability and hardness have been achieved by the introduction of Si into TiN- or TiAlN-based coatings. JP 2000-334607 discloses a coated tool with laminated layers comprising TiSi (layer a) and TiAl (layer b) compounds. The (a) layer is selected among nitride, carbonitride, oxynitride and oxycarbonitride containing 10%<Si<60% with a NaCl type crystalline structure. Layer (b) is selected among nitride, carbonitride, oxynitride and oxycarbonitride containing 40%<Al<75% with a NaCl type crystalline structure. The (a) layer and (b) layers are applied alternately by each one layer or more and the (b) layer is located just above the surface of the base material.

EP 1939327 discloses a cutting tool comprising a hard coating giving improved crater and flank wear resistance, said coating comprising an aperiodic multilayer X+Y+X+Y+ . . . with average layer thickness of X and Y layers of between 0.1 and 100 nm and with average chemical composition Al a Ti b Si c Cr d C e N 1-e , where 0<a<0.5, 0.1<b<0.9, 0.01<c<0.17, 0≦d<0.06, a+b+c+d=1, and 0≦e<1.

The trends towards dry-work processes for environmental protection, i.e., metal cutting operation without using cutting fluids (lubricants) and accelerated machining speed with improved process put even higher demands on the characteristics of the tool materials due to an increased tool cutting-edge temperature. In particular, coating stability at high temperatures, e.g., oxidation- and wear-resistance have become even more crucial.

›SUMMARY OF THE INVENTION

It is an object of the present invention to provide a coated cutting tool yielding improved performance in metal cutting applications at elevated temperatures.

It is a further object of the present invention to provide a coated cutting tool with improved edge integrity.

It has been found that combining layers based on (Ti,Si)N and (Ti,Al)N, respectively, in a nanolaminated coating structure onto a cubic boron nitride based cutting tool insert significantly improves the tool life due to increased crater wear resistance, flank wear resistance and edge integrity, especially in high speed machining operations generating high tool temperatures.

›BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1 ; Scanning electron microscopy (SEM) image showing a fractured cross section of a Ti 0.38 Al 0.62 N/Ti 0.86 Si 0.14 N nanolaminated structure.

FIG. 2 ; Scanning electron microscopy (SEM) images showing examples of the cutting edges after 24 minutes of turning in case hardened steel with (a) Ti 0.86 Si 0.14 N single layer and (b) Ti 0.38 Al 0.62 N/Ti 0.86 Si 0.14 N nanolaminated structure.

›DETAILED DESCRIPTION OF THE INVENTION

According to the present invention, there is provided a cutting tool for machining by chip removal comprising a body of polycrystalline cubic boron nitride compact (PCBN), either as a solid insert or attached to a backing body, onto which is deposited a hard and wear resistant coating comprising a polycrystalline nanolaminated structure of alternating A and B layers with a thickness between 0.5 and 10 μm, preferably between 0.5 and 5 μm, and with an overall columnar structure. The average column width is between 20 and 1000 nm, preferably between 20 and 500 nm, as determined by, e.g., cross section scanning electron microscopy of a middle region of the nanolaminated structure, i.e., in a region within 30 to 70% of the thickness in the growth direction, and said average columnar width is the average from measuring the width of at least ten adjacent columns.

Said layer A is (Ti 1-x-p Al x Me1 p )N a , where 0.3<x<0.95, preferably 0.45<x<0.75, and 0.90<a<1.10, preferably 0.96<a<1.04, 0≦p<0.15, and Me1 is one or more of the metal elements from group 3, 4, 5 or 6 in the periodic table, preferably one or more of Zr, Y, V, Nb, Mo and W, most preferably one or more of Zr, Y, V and Nb. Said layer B is (Ti 1-y-z Si y Me2 z )N b , where 0.05<y≦0.25 preferably 0.05<y<0.18, 0≦z<0.4, 0.9<b<1.1, preferably 0.96<b<1.04, and Me2 is one or more of the metal elements from group 3, 4, 5 or 6 in the periodic table including Al, preferably one or more of Y, V, Nb, Mo, W and Al, most preferably one or more of Y, V, Nb and Al. Layers A and B have an average individual layer thickness between 1 nm and 50 nm, as measured by, e.g., cross sectional transmission electron microscopy of a middle region of the nanolaminated structure, i.e., a region within 30 to 70% of the thickness in the growth direction, and said average layer thickness is the average from measuring the thickness of at least ten adjacent layers. Said nanolaminated structure comprises a phase mixture of cubic and hexagonal phases, preferably only cubic phases, as determined by X-ray diffraction.

In a first preferred embodiment z=p=0.

In a second preferred embodiment Me1 is one or more of Zr, Y, V and Nb with 0<p<0.05.

In a third preferred embodiment Me2 is Y, 0<z<0.15.

In a fourth preferred embodiment Me2 is one or both of V and Nb with 0<z<0.3.

In a fifth preferred embodiment Me2 is Al, 0.2<z<0.4.

The average composition of said nanolaminated structure is 45 at %<Ti+Al+Si+Y+V+Nb+Mo+W+Zr<55 at %, preferably 48 at %<Ti+Al+Si+Y+V+Nb+Mo+W+Zr<52 at % and rest N as determined by, e.g., EDS or WDS techniques.

Said coating may comprise an inner single- and/or multilayer coating of TiN, TiC, Ti(C,N) or (Ti,Al)N, preferably (Ti,Al)N, and/or an outer single- and/or multilayer coating of TiN, TiC, Ti(C,N), (Ti,Si)N or (Ti,Al)N, preferably (Ti,Si)N or (Ti,Al)N, according to known art, to a total coating thickness, including the thickness of the nanolaminated structure, of between 0.5 and 20 μm, preferably between 0.5 and 10 μm, and most preferably between 0.5 and 7 μm.

Said PCBN body contains at least 30 vol % of cubic phase boron nitride (cBN) in a binder. The binder contains at least one compound selected from a group consisting of nitrides, borides, oxides, carbides and carbonitrides of one or more of the elements belonging to the groups 4, 5 and 6 of the periodic table and Al, e.g., Ti(C,N) and AlN.

In a sixth preferred embodiment, said PCBN body contains 30 vol %<cBN<70 vol %, preferably 40 vol %<cBN<65 vol %, with an average cBN grain size between 0.5 μm and 4 μm. The binder contains 80 wt %<Ti(C,N)<95 wt % and rest containing mainly other compounds comprising two or more of the elements Ti, N, B, Ni, Cr, Mo, Nb, Fe, Al and/or O, e.g., TiB 2 and Al 2 O 3 .

In a seventh preferred embodiment, said PCBN body contains 45 vol %<cBN<70 vol %, preferably 55 vol %<cBN<65 vol %, with an average cBN grain size between 0.5 μm and 4 μm, preferably between 1 μm and 3 μm. The binder contains 80 wt %<Ti(C,N)<90 wt %, 1 wt. %<alloy containing one or more of the elements Ni, Co, Cr and/or Mo<10 wt %, and rest containing mainly TiB 2 and Al 2 O 3 .

In an eighth preferred embodiment, said PCBN body contains 70 vol %<cBN, preferably 80 vol %<cBN<95 vol %, with an average cBN grain size either between 0.5 μm and 10 μm, preferably between 1 μm and 6 μm, or between 10 μm and 25 μm, preferably between 15 μm and 25 μm. The binder contains compounds of two or more of the elements Al, B, N, W, Co, Ni, Fe, Al and/or O.

The deposition method for the coatings of the present invention is based on cathodic arc evaporation of an alloy or composite cathode under the following conditions; (Ti,Al,Me1)N and (Ti,Si,Me2)N layers are grown from cathodes yielding the desired layer composition. The evaporation current is between 50 A and 200 A. The layers are grown in an Ar+N 2 atmosphere, preferably in a pure N 2 atmosphere, at a total pressure of 0.5 Pa to 9.0 Pa, preferably 1.5 Pa to 5.0 Pa. The bias is −10 V to −300 V, preferably −20 V to −200 V. The deposition temperature is between 350° C. and 700° C., preferably between 400° C. and 650° C.

The invention also relates to the use of cutting tool inserts according to the above for machining of steels, cast irons, super alloys and hardened steels at cutting speeds of 50-2000 m/min, preferably 50-1500 m/min, with an average feed of 0.01-1.0 mm/rev, preferably 0.01-0.6 mm, depending on the cutting operation.

›Examples5
›Example 1

The coatings of Table 1 were deposited by cathodic arc evaporation onto the following PCBN inserts:

S1 with 60 vol % cBN, an average cBN grain size of about 2 μm and a binder containing 86 wt % Ti(C,N), 5 wt % ASTM F75 alloy (main composition: 62 wt % Co+28.5 wt % Cr+6 wt % Mo) and rest containing mainly TiB 2 and Al 2 O 3 . S2 with 60 vol % cBN, an average cBN grain size of about 2 μm and a binder containing 86 wt % Ti(C,N), 5 wt % Inconel 625 alloy (main composition: 28.5 wt % Cr+9 wt % Mo+3 wt. % Nb+balance Ni) and rest containing mainly TiB 2 and Al 2 O 3 . S3 with 50 vol % cBN, an average cBN grain size of about 1 μm and a binder containing 91 wt % Ti(C,N) and rest containing mainly TiB 2 and Al 2 O 3 . S4 with 90 vol % cBN, an average cBN grain size of about 4 μm and a binder containing mainly AlN and rest containing mainly AlB 2 .

S5 with 90 vol % cBN, an average cBN grain size of about 20 μm and a binder containing mainly AlN and rest containing mainly AlB 2 .

Before deposition, the inserts were cleaned in ultrasonic baths of an alkali solution and alcohol. The deposition chamber was evacuated to a base pressure of less than 2.0×10 −3 Pa, after which the inserts were sputter cleaned with Ar ions. The coatings were deposited from alloy or composite cathodes in 99.995% pure N 2 atmosphere at a total pressure of 2-6 Pa, using a bias of −20 to −60 V and an evaporation current of 60-200 A. The cathodes were selected to yield the composition of Layer A and Layer B, respectively, and mounted on opposing sides of the deposition chamber in order to obtain the nanolaminated structure by fixture rotation. The average individual layer thickness was varied by altering the cathode current (60-200 A) and the rotation speed of the fixture (1-5 rpm). The total coating thicknesses were about 2 μm for all inserts and the deposition temperature was 450° C.

FIG. 1 shows an example of a scanning electron microscopy (SEM) image of a Ti 0.38 Al 0.62 N/Ti 0.86 Si 0.14 N nanolaminated structure (coating 1) with a columnar microstructure that extends throughout the nanolaminated structure. The individual layers are clearly seen, indicating minimal intermixing between adjacent layers, and the individual layer thickness varies due to a 3-fold fixture rotation.

The total average composition of the coatings was measured by energy dispersive x-ray spectroscopy (EDS) analysis area using a LEO Ultra 55 scanning electron microscope with a Thermo Noran EDS detector operating at 10 kV. The data were evaluated using a Noran System Six (NSS ver 2) software.

›Example 2

Coatings 1, 3, 6, 40-45 on S1 and S2 inserts were tested under the following conditions:

Geometry: CNGA120408S

Application: Continuous turning

Work piece material: Case hardened steel (16MnCr5)

Cutting speed: 200 m/min

Feed: 0.1 mm/rev

Depth of cut: 0.15 mm

Tool life criteria: Edge failure

The results are shown in Table 2.

FIG. 2 shows SEM images of used edges of S1 inserts after 24 minutes turning with (a) comparative coating 41 and (b) inventive coating 1. It is clearly seen that the inventive coating show improved crater and edge wear characteristics.

›Example 3

Coatings 1-6, 35, 36, 38-42, 44-45 on S3 inserts were tested under the following conditions:

Geometry: RCGN0803MOS

Application: Continuous turning

Work piece material: Case hardened steel (16MnCr5)

Cutting speed: 200 m/min

Feed: 0.1 mm/rev

Depth of cut: 0.15 mm

Tool life criteria: Edge failure

The results are shown in Table 2.

›Example 4

Coatings 6, 37, 40, 41 on S4 inserts were tested under the following conditions:

Geometry: CNMN120412S

Application: Facing

Work piece material: AISI A48-40B

Cutting speed: 1100 m/min

Feed: 0.3 mm/rev

Depth of cut: 1 mm

Tool life criteria: Edge failure

The results are shown in Table 2.

›Example 5

Coatings 6, 40, 41 on S5 inserts were tested under the following conditions:

Geometry: CNMN120412S

Application: Continuous turning

Work piece material: AISI A48-45B

Cutting speed: 1100 m/min

Feed: 0.4 mm/rev

Depth of cut: 2 mm

Tool life criteria: Edge failure

The results are shown in Table 2.

It is obvious from the above examples that the inserts according to the invention show an increased tool performance with improved edge and crater wear characteristics.

›Tables in the description — 2
TABLE 1 — *Individual layer compostions are estimated from the corresponding single layers. **Constant individual layer thicknesses. ***Me2 content excluding Al, which has its own column. ****A bottom Ti 0.38 Al 0.62 N layer (0.3 μm thickness) and a top Ti 0.38 Al 0.62 N layer (0.3 μm) were applied to a total coating thickness of 2 μm.
Composition Layer AComposition Layer BAverage compositionLayer thickn.
(metal at.%)(metal at.%)(at.%)(nm)
CoatingDescriptionTiAlSiMe1TiAlSiMe2***TiAlSiMe1Me2***NAB
Inventive
1TiAlN/TiSiN*38620086014031.912.64.10.00.051.458
2TiAlN/TiSiN*38620086014039.15.75.60.00.049.6417
3TiAlN/TiSiN*38620086014026.121.22.20.00.050.4115
4TiAlN/TiSiN*38620086014034.311.84.50.00.049.435
5TiAlN/TiSiN*38620086014027.918.52.90.00.050.62417
6TiAlN/TiSiN* , ****38620086014032.912.74.30.00.050.158
7TiAlN/TiSiN* , **38620086014031.414.43.80.00.050.378
8TiAlN/TiSiN*50500086014033.113.13.40.00.050.5109
9TiAlN/TiSiN*3862009307035.313.61.90.00.049.168
10TiAlN/TiSiN*3862009307032.116.31.70.00.050.096
11TiAlN/TiSiN*5050009307038.710.42.00.00.048.956
12TiAlN/TiSiYN*38620084012429.516.72.80.01.050.11110
13TiAlN/TiSiYN*3862008309831.912.82.60.02.350.446
14TiAlN/TiSiYN*38620079071428.716.71.60.03.349.887
15TiAlN/TiSiVN*38620082011732.513.93.10.02.048.579
16TiAlN/TiSiVN*38620076091527.017.72.10.03.350.0108
17TiAlN/TiSiVN*50500070072332.49.52.10.07.148.858
18TiAlN/TiSiNbN*38620085010531.113.62.90.01.451.0912
19TiAlN/TiSiNbN*38620078081427.916.81.90.03.350.187
20TiAlN/TiSiNbN*38620069062526.114.31.60.06.651.356
21TiAlN/TiSiAlN*386200672112029.418.43.60.00.048.658
22TiAlN/TiSiAlN*38620055396022.325.91.60.00.050.356
23TiAlN/TiSiAlN*38620060328024.522.62.10.00.050.767
24TiAlYN/TiSiN*38610186014034.011.94.20.40.049.869
25TiAlYN/TiSiN*37590486014034.412.34.21.00.049.157
26TiAlVN/TiSiN*38610186014032.611.74.20.40.051.558
27TiAlVN/TiSiN*37590486014034.712.63.91.00.048.868
28TiAlNbN/TiSiN*38610186014034.412.54.30.40.048.969
29TiAlNbN/TiSiN*37590486014034.311.24.21.00.050.358
30TiAlZrN/TiSiN*38610186014031.714.43.90.50.050.167
31TiAlZrN/TiSiN*37590486014032.413.34.01.10.050.379
32TiAlZrN/TiSiVN*38610176091529.313.02.60.44.350.857
33TiAlZrN/TiSiYN*37590484012433.811.33.70.91.249.958
34TiAlVN/TiSiAlN*37590460328023.722.92.10.90.051.367
Comparative
35TiN/TiSiN*10000086014045.40.04.10.00.050.5912
36TiAlSiN/TiSiN*6132709307036.79.53.50.00.050.3107
37l8020009307044.05.01.80.00.049.299
38TiAlN/TiSiN* , **38620086014027.619.22.70.00.050.613080
39TiN/TiAlSiN* , **10000061327039.38.71.90.00.050.1110130
40TiAlN37.662.40.00.00.00.00.00.0—————50.4——
41TiSiN86.40.013.60.00.00.00.00.0—————49.5——
42TiSiN92.80.07.20.00.00.00.00.0—————49.6——
43TiAlSiN61.132.06.90.00.00.00.00.0—————50.0——
44TiSiN + TiAlN**85.90.014.10.038.062.00.00.0N (at. %): 51.1/49.510801250
45TiAlN + TiSiN**38.361.70.00.086.00.014.00.0N (at. %): 50.1/50.51140870
TABLE 2
Example 2Example 4Example 5
Life time (min)Example 3LifeLife
CoatingCraterEdgeS1 insertsS2 insertsCraterEdgeLife time (min)time (min)time (min)
Inventive
1GoodGood3633GoodGood27——
2————GoodMedium24——
3Good/MediumGood3331MediumGood27——
4————Good/MediumGood/Medium21——
5————Good/MediumMedium21——
6GoodGood3630GoodGood309060
Comparative
35————MediumMedium18——
36————GoodMedium/Poor21——
37———————70—
38————GoodPoor15——
39————GoodPoor18——
40PoorGood2121PoorGood156045
41GoodPoor2724Good/MediumPoor217050
42MediumMedium2424MediumMedium18——
43Good/MediumPoor2124—————
44MediumMedium1518Good/MediumMedium/Poor15——
45GoodMedium/Poor1818GoodMedium/Poor18——

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Classifications

14 codes
IPC · International Patent Classification
Section C — Chemistry; metallurgy
  • C23C14/00
  • C04B41/52
  • C23C14/06
  • C23C30/00
  • C04B41/00
  • C04B41/89
USPC · US Patent Classification
51/307428/472428/216428/336428/699428/697428/469204/192.1

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