HARD COATING FOR CUTTING TOOLS WITH EXCELLENT WEAR RESISTANCE

Information

  • Patent Application
  • 20240216999
  • Publication Number
    20240216999
  • Date Filed
    December 05, 2023
    a year ago
  • Date Published
    July 04, 2024
    7 months ago
Abstract
The purpose of the invention is to provide a hard coating for cutting tools, wherein the hard coating is excellent in wear resistance and oxidation resistance, as well as in hardness properties. In order to achieve the purpose, the invention may provide a cutting tool which includes a hard substrate and a hard coating formed on the hard substrate, wherein the hard coating has a structure in which a first sub-coating having a composition range represented by [Formula 1] below and having a cubic structure, and a second sub-coating having a composition range represented by [Formula 2] below and having a cubic structure are alternately stacked.
Description
BACKGROUND OF THE INVENTION
1. Field of the Invention

The present invention relates to a hard coating formed on a hard base material, such as cemented carbide, cermet, ceramic, and cubic boron nitride used in a cutting tool, and more specifically, to an AlMnN-based hard coating of a cubic structure formed on a hard substrate.


2. Description of the Related Art

In a cutting tool, oxidation and deterioration of continuously occur on a cutting blade due to heat generated during a cutting process. As a result, the cutting blade has reduced hardness and is embrittled, causing the tool to be easily damaged.


In order to address the limitation, a method of depositing a thin film of TiN, TiAlN, AlN, or Al2O3, which is a hard coating, on a hard substrate such as cemented carbide, cermet, ceramic, or cubic boron nitride, is used. There is a continuous demand for extending the lifespan of a tool by improving oxidation resistance and mechanical strength through such a hard coating.


In hard coatings, AlXN(wherein X is a transition metal)-based thin films are excellent in wear resistance and oxidation resistance, and thus, are most widely used as coatings for cutting tools. In such a hard coating, the greater the Al content, the more excellent are oxidation resistance and wear resistance. However, although there is a difference depending on an X element, when the content of an Al element is about 50% to 70% or greater, there is a problem in that the hardness is drastically reduced as the hard coating has a crystal structure of a B4 hexagonal crystal structure.


SUMMARY OF THE INVENTION

The purpose of the invention is to provide a hard coating for cutting tools, wherein the hard coating is excellent in wear resistance and oxidation resistance, as well as in hardness properties.


According to an aspect of the invention, there is provided a cutting tool which includes a hard substrate and a hard coating formed on the hard substrate, wherein the hard coating has a structure in which a first sub-coating having a composition range represented by [Formula 1] below and having a cubic structure, and a second sub-coating having a composition represented by [Formula 2] below and having a cubic structure are alternately stacked.




embedded image



MeN(Here, Me includes one or more selected among Ti, Cr, Zr, Hf, V, Nb, Ta, Mo, and Al)  [Formula 2]


In addition, in the cutting tool according to an embodiment of the invention, x in [Formula 1] above may be in the range of 0.005×0.05.


In addition, in the cutting tool according to an embodiment of the invention, the sum of the thickness of one first sub-coating and the thickness of one second sub-coating, which are successive coatings, may be in the rage of 1 nm to 40 nm.


In addition, in the cutting tool according to an embodiment of the invention, the thickness of the hard coating may be in the range of 0.5 μm to 20 μm.


In addition, in the cutting tool according to an embodiment of the invention, the hard coating may not show a B4 hexagonal structure in analysis through XRD.


In addition, in the cutting tool according to an embodiment of the invention, the difference between the lattice constant of the first sub-coating and the lattice constant of the second sub-coating may be 10% or less based on the lattice constant of the first sub-coating.


Advantageous Effects

According to the invention, it is possible to obtain a cutting tool having a hard coating, wherein the hard coating has high wear resistance and oxidation resistance, and at the same time, maintains high hardness.





BRIEF DESCRIPTION OF THE DRAWINGS


FIG. 1 is a graph showing hardness according to the content of Mn in an AlN-based hard coating;



FIG. 2 is a schematic diagram describing a cross-section of an embodiment of a cutting tool according to the invention;



FIG. 3 is a schematic diagram describing a cross-section of an embodiment of a cutting tool according to the invention; and



FIG. 4 is a schematic diagram describing a PVD sputtering coating system used to film a hard film according to the present invention.





DETAILED DESCRIPTION OF THE EXEMPLARY EMBODIMENTS

In the following description of the present invention, when it is determined that detailed descriptions of related known functions or configurations may unnecessarily obscure the gist of the present invention, the detailed descriptions will be omitted. In addition, when a portion is said to ‘include’ any component, it means that the portion may further include other components rather than excluding the other components unless otherwise stated.


The invention relates to a cutting tool including a hard substrate and a hard coating formed on the hard substrate, wherein the hard coating has a structure in which a first sub-coating having a composition range represented by [Formula 1] below and having a cubic structure, and a second sub-coating having a composition represented by [Formula 2] below and having a cubic structure are alternately stacked.





Al1-xMnxN(0.005≤x<0.1).  [Formula 1]





MeN(Here, Me includes one or more selected among Ti, Cr, Zr, Hf, V, Nb, Ta, Mo, and Al)  [Formula 2]


There are AlN-based coatings as hard coatings formed on hard substrates such as cemented carbide, cermet, ceramic, and cubic boron nitride to increase the cutting ability and durability of cutting tools while protecting the hard substrates. Among AlN-based hard coatings, AlTiN films generally have an Al content of 60% or less, and this is because when the Al content in an AlTiN-based coating is 70% or greater, the coating basically has a B4 hexagonal structure and has a hardness of about 16 GPa or less, which makes it less effective to use the coating as a coating for cutting tools.


From the graph of FIG. 1 derived through the First-principles calculation, the inventors of the invention have confirmed that an AlMnN-based coating may have more excellent mechanical properties when the coating has a cubic structure rather than a hexagonal structure, and particularly, AlN having a cubic structure and containing a small amount of Mn may have an increased hardness of about 38 GPa.


However, the stable phase of an AlN-based coatings is a hexagonal structure, and there is a difficulty in stably forming and maintaining a cubic structure only with an AlMnN coating containing a small amount of Mn. In order to address the limitation, in the invention, a first sub-coating, which is an AlMnN coating, and a second sub-coating, which is an MeN coating of another cubic structure may be alternately stacked to obtain a hard coating with excellent mechanical strength. By forming a nano-multilayer composed of the first sub-coating and the second sub-coating as described above, a superlattice is formed and a hard coating of a stable cubic structure may be formed and maintained.


The first sub-coating is an AlMnN coating and has the formula of Al1-xMnxN, wherein x is in the rage of 0.005 to 0.1.


When x is 0.005 or greater, it is possible to form a cubic AlMnN coating with higher hardness compared to AlN, and when greater than 0.1, the hardness may be degraded. This can be seen in FIG. 1, which predicts the hardness of an AlMnN hard coating according to an Mn content, and it can be seen that the hardness of an AlMnN hard coating having a cubic structure (B1) is higher than that of an AlMnN hard coating having a hexagonal structure (B4), and that the content of Mn in the cubic structure (B1) reaches the maximum value when the value of x in [Formula 1] is 0.03 and decreases thereafter. Therefore, the value of x in [Formula 1] is preferably 0.005 to 0.1, and more preferably 0.005 to 0.05.


The second sub-coating is a metal nitride layer represented by [Formula 2], wherein Me, which is a metal, may include one or more selected among Ti, Cr, Zr, Hf, V, Nb, Ta, Mo, and Al.


These metal nitrides are advantageous in maintaining a cubical structure and may form a hard coating with excellent mechanical strength.


Meanwhile, the first sub-coating and the second sub-coating are alternately stacked, and the first sub-coating or the second sub-coating, which is repeated, may be stacked with the same composition, or the first sub-coating or the second sub-coating with a slightly different composition may be stacked.



FIGS. 2 and 3 are drawings which describe a hard coating formed on a hard substrate. FIG. 2 shows that a first sub-coating 31-1 and a second sub-coating 32-1, which are repeated when a hard coating 30 is formed on a hard substrate 20, are repeatedly and alternately stacked in succession with the same composition. It shows that a group of sub-coatings 33, which is composed of the first sub-coating 31-1 and the second sub-coating 32-1, is repeatedly stacked.


In comparison, FIG. 3 is a drawing which describes that when repeated first sub-coatings 31-1 and 31-2 are alternately stacked with second sub-coatings 32-1 and 32-2, four sub-coatings with different compositions are alternately stacked. That is, the first sub-coating 31-1 and another first sub-coating 31-2 have different compositions, and the second sub-coating 32-1 and another second sub-coating 32-2 have different compositions. It shows that a group sub-coatings 34, which is composed of the first sub-coating 31-1, the second sub-coating 32-1, the first sub-coating 31-2, and the second sub-coating 32-2, is repeatedly stacked.


In the cutting tool according to the invention, the sum of the thickness of one first sub-coating and the thickness of one second sub-coating, which are successive coatings, may be in the rage of 1 nm to 40 nm.


Since the first sub-coating and the second sub-coating are continuous with each other and form a superlattice structure, an AlMnN coating of the first sub-coating may maintain a stable cubic structure. To this end, it is necessary that the sum of the thickness of one first sub-coating and the thickness of one second sub-coating, which are successive coatings, is 40 nm or less. If thicker than the above, it may be difficult to maintain the superlattice structure. In addition, if too thin, a multi-layered crystal lattice may not be exhibited, so it is necessary that the sum is 1 nm or greater.


In addition, in the cutting tool according to the invention, the thickness of the hard coating may be in the range of 0.5 μm to 20 μm. If the total thickness of the hard coating including the first sub-coating and the second sub-coating alternately stacked is less than 0.5 μm, which is too thin, sufficient wear resistance and oxidation resistance may not be achieved, and if greater than 20 μm, which is too thick, a peeling problem may occur due to internal stress.


In addition, in the cutting tool according to the invention, the hard coating may not show a B4 hexagonal structure in analysis through XRD.


As described above, the hard coating may exhibit better mechanical properties when having a cubic structure. Therefore, the hard coating according to the invention may be a hard coating of a cubic structure which does not include a hexagonal structure.


In addition, the difference between the lattice constant of the first sub-coating and the lattice constant of the second sub-coating may be 10% or less based on the lattice constant of the first sub-coating. If the difference in the lattice constant is too large, the bonding force between sub-coatings may decrease, and the internal stress may be increase, which is not preferable.


Hereinafter, in order to describe the invention in more detail, preferred embodiments according to the invention will be described in more detail. However, the invention is not limited to the embodiments described herein.


Example 1

In order to select a target material, the structure and mechanical properties of ternary nitrides (Ti1-xMx)N and (Al1-xMx)N were confirmed by performing the First-principles calculation based on an electron density theory based on the Vienna ab initio simulation package (VASP) code. The results are shown in [Table 1] below.


A target composition having a lattice constant difference of 10 or less was preferentially selected in order to form a superlattice during the formation of an Al1-xMnxN/MeNbased film.














TABLE 1








Lat-
Lattice






tice
constant




Metal

con-
differ-
Elastic


Thin
element
Struc-
stant
ence
modulus


film
ratio (at %)
ture
[A]
(%)
[GPa]





















AlMnN
Al:Mn =
97:3
B1
4.07
0  
506.67


TiN
Ti =
100
B1
4.23
4%
473.35


CrN
Cr =
100
B1
4.05
0%
158.28


ZrN
Zr =
100
B1
4.59
13% 
368.77


HfN
Hf =
100
B1
4.53
11% 
390.13


VN
V =
100
B1
4.12
1%
400.37


NbN
Nb =
100
B1
4.45
9%
320.09


TaN
Ta =
100
B1
4.25
4%
447.24


MoN
Mo =
100
B1
4.35
7%
302.09


TiAlN
Ti:Al =
50:50
B1
4.18
3%
452.18


CrAlN
Cr:Al =
50:50
B1
4.09
0%
380.69


ZrAlN
Zr:Al =
50:50
B1
4.38
8%
378.45


HfAlN
Hf:Al =
50:50
B1
4.35
7%
407.44


VAlN
V:Al =
50:50
B1
4.10
1%
458.90


NbAlN
Nb:Al =
50:50
B1
4.28
5%
416.82


TaAlN
Ta:Al =
50:50
B1
4.28
5%
429.73


MoAlN
Mo:Al =
50:50
B1
4.25
4%
368.28


CrTiN
Cr:Ti =
50:50
B1
4.16
2%
343.12


ZrTiN
Zr:Ti =
50:50
B1
4.44
9%
393.12


HfTiN
Hf:Ti =
50:50
B1
4.41
8%
418.24


VTiN
V:Ti =
50:50
B1
4.19
3%
411.58


NbTiN
Nb:Ti =
50:50
B1
4.36
7%
365.14


TaTiN
Ta:Ti =
50:50
B1
4.34
7%
371.02


MoTiN
Mo:Ti =
50:50
B1
4.30
6%
352.75









<Formation of Hard Coating>

An Al1-xMnxN/MeN-based nano-multilayer thin film was formed using a PVD sputtering coating system as shown in FIG. 4. The thin film was manufactured by controlling coating, after vacuum evacuation to 5×10−5 Torr, under the conditions of a film formation substrate temperature of 500° C., a process pressure of 7 m Torr, a gas flow rate ratio of Ar:N2=6:1, a target power of 700 W, a substrate bias of −100 V, and a table rotation speed of 3 RPM to 0.2 RPM depending on a deposition rate, and the film formation was performed with a coating thickness of about 2 μm.


The thickness of the thin film was measured using a scanning electron microscope (SEM) on a fractured surface of the manufactured sample, and the stacking cycle was calculated by dividing the measured thickness of the thin film by the number of rotations of the table during the coating. The hardness was measured using the HM2000 equipment by Helmut Fischer company. The crystal structure of the thin film was analyzed using an X-ray diffraction analyzer.


The cutting evaluation was conducted by measuring the total chip removal amount using a vertical machining center. A test sample was prepared by depositing a coating on a substrate with the model name of ADKT120408PDSR-ML and the grade name of PP5300.


A material to be cut was evaluated under the wet processing conditions of an Inconel of 718, a cutting speed of 35 m/min, a feed of 0.11 vmm/t, an axial direction cutting depth (ap) of 5 mm, a radial direction cutting depth (ae) of 3.1 mm, and a milling cutter diameter of 32 mm (4 blades). The termination point of time for horizontal determination was set to an uniform width of flank wear (VB) of 3.5 mm or greater or an uneven chipping amount of 1.2 mm or greater.


The results of evaluating physical properties in accordance therewith are shown in Table 2 below.











TABLE 2









Analysis









Cutting














Target composition
Stacking



process



(at %)
cycle
Thickness
Hardness
Crystal
amount














Classification
Target A
Target B
(nm)
[μm]
[GPa]
structure
(cm3)

















Comparative
Al97Mn3


2.5
14.3
B4
53


Example 1


Comparative

Ti

2.1
14.6
B1
37


Example 2


Example 1
Al97Mn3
Ti
9
1.8
24.5
B1
323


Comparative
Al97Mn3
Ti
82
1.7
19.4
B1, B4
77


Example 3


Comparative

Ti5Al5

2.6
18.7
B1
107


Example 4


Example 2
Al97Mn3
Ti5Al5
8
1.9
25.6
B1
431


Comparative
Al97Mn3
Ti5Al5
80
1.8
20.8
B1, B4
77


Example 5


Comparative

Cr

2.8
20.9
B1
107


Example 6


Example 3
Al97Mn3
Cr
9
2.6
24.1
B1
215


Comparative

Cr5Ti5

2.5
13.0
B1
53


Example 7


Example 4
Al97Mn3
Cr5Ti5
10
2.6
24.1
B2
323


Comparative

Cr5Al5

2.7
18.7
B1
107


Example 8


Example 5
Al97Mn3
Cr5Al5
9
2.3
24.1
B1
323


Comparative

Zr

1.8
16.7
B1
107


Example 9


Comparative
Al97Mn3
Zr
11
2.3
19.7
B1
77


Example 10


Comparative

Zr5Al5

2.3
20.3
B1
77


Example 11


Example 6
Al97Mn3
Zr5Al5
12
2.8
29.1
B1
323


Comparative

Zr5Ti5

3.0
19.7
B1
107


Example 12


Example 7
Al97Mn3
Zr5Ti5
8
1.9
27.5
B1
269


Comparative

Nb

1.7
24.8
B1
37


Example 13


Example 8
Al97Mn3
Nb
11
2.0
33.7
B1
161


Comparative

Nb5Al5

2.4
20.7
B1
107


Example 14


Example 9
Al97Mn3
Nb5Al5
10
2.2
29.8
B1
215


Comparative

Nb5Ti5

2.2
18.3
B1
77


Example 15


Example 10
Al97Mn3
Nb5Ti5
11
2.4
29.3
B1
215


Comparative

Hf

1.7
16.9
B1
37


Example 16


Comparative
Al97Mn3
Hf
12
2.5
22.4
B1
53


Example 17


Comparative

Hf5Al5

2.1
22.2
B1
77


Example 18


Example 11
Al97Mn3
Hf5Al5
10
2.0
31.1
B1
161


Comparative

Hf5Ti5

1.8
21.7
B1
53


Example 19


Example 12
Al97Mn3
Hf5Ti5
11
2.6
28.9
B1
215


Comparative

V

1.9
14.7
B1
37


Example 20


Example 13
Al97Mn3
V
9
2.1
27.8
B1
161


Comparative

V5A15

1.8
24.6
B1
77


Example 21


Example 14
Al97Mn3
V5A15
9
1.6
31.8
B1
269


Comparative

V5Ti5

1.7
16.0
B1
77


Example 22


Example 15
Al97Mn3
V5Ti5
10
1.8
26.6
B1
215


Comparative

Ta

1.9
9.6
B1
37


Example 23


Example 16
Al97Mn3
Ta
8
1.6
24.7
B1
161


Comparative

Ta5Al5

2.1
20.9
B1
107


Example 24


Example 17
Al97Mn3
Ta5Al5
10
2.3
26.7
B1
161


Comparative

Ta5Ti5

1.7
13.4
B1
77


Example 25


Example 18
Al97Mn3
Ta5Ti5
11
2.5
26.2
B1
215


Comparative

Mo

1.8
9.8
B1
53


Example 26


Example 19
Al97Mn3
Mo
9
1.8
23.5
B1
215


Comparative

Mo5Al5

2.1
16.5
B1
53


Example 27


Example 20
Al97Mn3
Mo5Al5
10
2.2
21.2
B1
161


Comparative

Mo5Ti5

2.1
12.9
B1
37


Example 28


Example 21
Al97Mn3
Mo5Ti5
10
2.0
22.1
B1
161








Claims
  • 1. A cutting tool comprising a hard substrate and a hard coating formed on the hard substrate, wherein the hard coating has a structure in which a first sub-coating having a composition range represented by [Formula 1] below and having a cubic structure and a second sub-coating having a composition represented by [Formula 2] below and having a cubic structure are alternately stacked: MeN(Here, Me includes one or more selected among Ti, Cr, Zr, Hf, V, Nb, Ta, Mo, and Al)  [Formula 2]
  • 2. The cutting tool according to claim 1, wherein in [Formula 1] above, x is in the range of 0.005≤x≤0.05.
  • 3. The cutting tool according to claim 1, wherein the sum of the thickness of one first sub-coating and the thickness of one second sub-coating, which are successive coatings, is in the rage of 1 nm to 40 nm.
  • 4. The cutting tool according to claim 1, wherein the thickness of the hard coating is in the range of 0.5 μm to 20 μm.
  • 5. The cutting tool of claim 1, Wherein the hard coating does not show a B4 hexagonal structure in analysis through XRD.
  • 6. The cutting tool of claim 1, Wherein the difference between the lattice constant of the first sub-coating and the lattice constant of the second sub-coating is 10% or less based on the lattice constant of the first sub-coating.
Priority Claims (1)
Number Date Country Kind
10-2022-0181851 Dec 2022 KR national