Gradient hardmetal with alternative binders

Abstract

The present invention relates to a cemented carbide comprising eta phase and a Ni-Al binder, the binder comprising intermetallic compound y'-Ni3Al- precipitates embedded in a substitutional solid solution matrix comprising Al and Ni, and further comprising a surface zone free of eta phase.

Description

[Technical field]

[0001] The present invention relates to a cutting tool comprising a cemented carbide substrate comprising tungsten carbide and a binder, the binder comprising y'-precipitates in a substitutional solid solution matrix, the cemented carbide comprising eta-phase, and further comprising a surface zone that is free of eta-phase and has less binder than an inner portion of the cemented carbide. [Background technology]

[0002] Cemented carbide based on tungsten carbide (WC) with cobalt binder has been known in the art since the 20's. Other metals known as binder metals in cemented carbide are iron and nickel, but cobalt is by far the most used.

[0003] Due to environmental and health impacts, efforts are ongoing to find alternative binders to cobalt. However, it is difficult to replace or limit the amount of cobalt without adversely affecting the material properties. For cutting tools, the substrate properties are critical to the overall performance of the tool, and even small changes in composition can have a detrimental effect on performance.

[0004] Nickel exhibits good wettability with WC, making it suitable for the production of hard alloys. Ni also performs better in oxidation and corrosion conditions compared to WC-Co hard alloys. The main drawback of Ni-based hard alloys is their reduced mechanical strength. One reason is that the stacking fault energy of Ni is higher compared to Co, making the work hardening of Ni moderate compared to Co.

[0005] To overcome the performance shortcomings of WC-Ni hardmetals, different methods have been proposed to increase the strength and / or hardness, such as producing sub-micrometer or near-nano WC-Ni hardmetals (Hall-Petch relationship) by inhibiting the growth of WC grains during sintering, or adding some elements to the matrix of WC-Ni hardmetals that promote high strength and / or hardness.

[0006] Such Ni-Al binders are known in hard metals. 3 Al is an intermetallic compound with high hardness and melting point. 3 Cemented carbides consisting of WC embedded in an Al binder have been reported to have high hardness and low toughness, making them less suitable for cutting tool substrates. Therefore, the NiAl binder needs to be optimized to achieve a binder with the desired properties (comparable to cobalt).

[0007] The eta phase can act as a reinforcement for the WC-binder composite to improve the hardness / toughness ratio of such hardmetals. However, for some applications it is necessary to optimize the hardness / toughness of the hardmetal near the surface. Summary of the Invention

[0008] It is an object of the present invention to provide a hardmetal with an alternative binder phase that has comparable or improved properties compared to a substrate with a Co binder.

[0009] It is also an object of the present invention to provide a method for producing y'-Ni in NiAl binder in a manufacturing process. 3 The present invention provides a hard metal having a NiAl binder that can control the formation of Al-precipitates.

[0010] It is also an object of the present invention to design a hard metal that can benefit from the advantages of eta phase while removing the eta phase from surface zones where it is not necessarily desired, producing a functionally graded (in microstructure and properties) hard metal. [Brief description of the drawings]

[0011] [Figure 1] 13 is a LOM image showing the gradient surface zone free of eta phase. [Diagram 2] 13 is a SEM image showing how the y'-Ni3Al-precipitates are embedded in the NiAl binder in the inner part. DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS

[0012] The present invention relates to a cutting tool comprising a cemented carbide substrate containing WC and 3-20% by weight of a binder, the binder being an intermetallic compound y'-Ni embedded in a substitutional solid solution matrix containing Al and Ni, with a weight ratio Al / Ni between 0.02 and 0.15, the total amount of Ni and Al being between 70 and 95% by weight of the binder. 3 The cemented carbide further comprises an inner portion and a surface zone having a depth between 5 and 400 μm, the inner portion comprising an amount of eta phase such that the volume fraction eta phase is between 1 and 30 volume percent, and the gradient surface zone is free of eta phase.

[0013] In the carburizing atmosphere, NiAl binder (Ni dispersed in the binder) 3 It has been discovered that by sintering a cemented carbide having eta phase (with Al precipitates) and eta phase, the eta phase can be dissolved at the surface of the cemented carbide to produce a graded composition within the sintered body with two distinct regions, one containing eta phase (inner portion) and one without eta phase (surface zone). This process also results in a redistribution of the binder phase, with less on the free surface of the eta phase compared to the inner portion.

[0014] According to the invention, the gradient surface zone is eta-phase free. The thickness of the gradient surface zone is suitably between 5 and 400 μm, preferably between 50 and 250 μm. The gradient surface zone is defined as the area between the surface of the tool and the point where eta phase begins to be present in the microstructure, i.e. the point where the inner part begins. The eta phase is most visible on cross-sectional polished surfaces of cemented carbide etched by LOM (10% Murakami solution, 1 sec).

[0015] The thickness is determined by measuring on SEM or LOM images of a cross section of the substrate. These measurements should be taken in areas where the substrate surface is reasonably flat, i.e. not close to an edge, at least 0.3 mm from the cutting edge, or nose, etc., to obtain a true value.

[0016] The gradient surface zone according to the present invention does not have eta-phase enrichment at the corners, i.e., the depth of the gradient surface is reasonably equal around the cutting tool indicating that the gradient formation is driven by carbon inter-diffusion.

[0017] In one embodiment of the present invention, the binder phase content in the gradient surface zone is lower than the binder phase content in the inner part of the cemented carbide. The binder phase content in the gradient surface zone is suitably 0.2-0.9 of the binder phase content in the bulk. The binder phase content in the gradient surface zone is preferably measured in the middle of the gradient surface zone, i.e. not close to the surface or boundary where eta phase starts to appear. One way to measure the binder phase content is by Microprobe Jeol JXA8530F equipped with an EDS / WDS detector. The boundary where the binder phase content no longer changes is not necessarily exactly the same depth as the depth of the gradient surface zone defined by where eta phase is present. This "binder phase surface gradient zone" defined by the binder phase content can have a smaller or larger depth than the gradient surface zone defined by eta phase, depending on the processing parameters.

[0018] Intermetallic compound y'-Ni 3 By Al-precipitates is meant herein semi-coherent precipitates having a cubic crystal structure (space group Pm-3m) that differs from the surrounding binder in that Al atoms preferentially occupy 1a sites and the solid solution binder exhibits random elemental occupancy at all sites.

[0019] Substitutional solid solutions are used herein to mean solid solutions in which the solvent and solute atoms are randomly located at lattice sites in the crystal structure of the phase. Elements such as C and N may also be present, but in interstitial sites.

[0020] Appropriately, y'-Ni 3 The average grain size of the Al precipitates is between 10 and 1000 nm, preferably between 10 and 500 nm. The precipitate grain size is suitably measured by image analysis on cross-sectional SEM images using the average linear intercept method.

[0021] y'-Ni 3 The Al precipitates are preferably present both in the gradient surface zone and in the inner part of the cemented carbide.

[0022] In one embodiment of the present invention, the y'-Ni 3 The average grain size of Al precipitates is 3 The average grain size of the y'-Ni Al precipitates is preferably smaller than that of the y'-Ni Al precipitates in the gradient surface zone. 3 The average grain size of Al precipitates is 3 This is less than 80% of the average grain size of the Al precipitates.

[0023] The amount of binder is preferably between 3 and 20% by weight of the hardmetal, preferably between 5 and 15%.

[0024] The weight ratio between Al / Ni is suitably between 0.02 and 0.15, preferably between 0.03 and 0.10, more preferably between 0.03 and 0.07.

[0025] The amount of Ni and Al is suitably 70-95% by weight of the binder, preferably 80-95% by weight, The remaining part of the binder is tungsten (W) which dissolves in the binder during sintering, possibly with the addition of other elements such as Cr.

[0026] The binder always contains a certain amount of W and C which dissolves during the sintering process from the WC. The exact amount depends on the overall composition of the cemented carbide.

[0027] The cemented carbide comprises an eta phase in an inner portion of the cemented carbide. As used herein, the eta phase is defined as Me, where Me is selected from W. 12 C and Me 6 C, and one or more of the binder phase metals.

[0028] The distribution of the eta phase in the cemented carbide should be as uniform as possible in that part of the cemented carbide where it is present, i.e. in the inner part.

[0029] In one embodiment of the present invention, the volume fraction of eta phase in the inner part of the cemented carbide is suitably between 1 and 30 vol%, preferably between 1.5 and 15 vol%, more preferably between 3 and 10 vol%, even more preferably between 3 and 6 vol%. Eta phase is most visible on cross-sectional polished surfaces of cemented carbide etched by LOM (10% Murakami solution, 1 sec). The amount of eta phase is preferably measured by image analysis. Measurements should also be avoided near the boundaries of gradient surface zones.

[0030] The average grain size of the eta phase precipitates is very difficult to measure because the eta phase particles are not round and in some cases look flower-like. The size of the eta phase precipitates depends on both the WC grain size and the amount of binder in the cemented carbide. The size of the eta phase precipitates in the inner part of the cemented carbide is preferably between 0.1 and 10 μm, more preferably between 0.1 and 3 μm, most preferably between 0.1 and 1 μm. It can be measured in various ways, for example by the average linear intercept on SEM / LOM images.

[0031] The eta phase in the inner portion of the cemented carbide is well distributed with the proper amount required to obtain improved properties. Well distributed eta phase is achieved by keeping the carbon content within certain limits. This is achieved by carefully controlling the carbon balance during manufacturing. Well distributed in this specification means that the cemented carbide does not contain large clusters of particles.

[0032] If the carbon content is too low, a large amount of eta phase will form. In practice, the maximum amount of eta phase desired in a cemented carbide depends on the particular application of the cutting tool. Too much eta phase can make the cemented carbide brittle. Thus, as a guideline, there should not be more than 30% by volume of eta phase in the cemented carbide, and preferably no more than 15% by volume.

[0033] If the carbon content is close to the limit where eta phase stops forming, there is a risk that the eta phase formed will be unevenly distributed, i.e. located in large clusters. This may be undesirable for certain applications. The difference in carbon content between achieving undesirable large clusters of eta phase and achieving the targeted finely distributed eta phase can be very small. Being close to that limit requires monitoring of the microstructure to ensure that undesirable large clusters are avoided. The limit at which finely distributed eta phase is achieved depends on the overall composition of the cemented carbide as known to those skilled in the art.

[0034] In one embodiment of the present invention, the cemented carbide is essentially free of Co, by which is meant herein that no Co is added as a raw material and any Co present in the cemented carbide is at impurity levels, preferably less than 1 wt%, more preferably less than 0.5 wt%. Small amounts of Co are typically found as some manufacturing equipment, such as grinding bodies, may contain cemented carbide and contribute little to the overall composition.

[0035] In one embodiment of the present invention, the cemented carbide is essentially free of Mo, by which is meant herein that Mo is not added as a raw material and that Mo is present in the cemented carbide at an impurity level, preferably less than 1% by weight relative to Mo.

[0036] Mo is undesirable in the materials herein since it can dissolve in the WC and either change its properties or form secondary carbides with a coarse structure similar to that of the binder, which severely embrittles it.

[0037] The term "hard metal" is intended herein to denote a material comprising a hard component in a metal binder phase, the hard component comprising at least 50% by weight of WC particles. The hard component may also comprise one or more carbides or carbonitrides of Ta, Ti, Nb, Cr, Hf, V and Zr, such as TiN, TiC and / or TiCN.

[0038] The average particle size of the WC is suitably between 0.2 and 10 μm, preferably between 0.4 and 5 μm, more preferably between 0.4 and 2 μm. The particle size can be measured, for example, by the mean linear intercept method.

[0039] In one embodiment of the present invention, the cemented carbide substrate is provided with a wear-resistant CVD (chemical vapor deposition) or PVD (physical vapor deposition) coating.

[0040] In one embodiment of the present invention, the cemented carbide substrate is provided with a wear resistant PVD coating, preferably one or more nitrides, oxides, carbides or mixtures thereof of elements selected from Al, Si and groups 4, 5 and 6 of the periodic table.

[0041] In yet another embodiment of the present invention, the cemented carbide substrate is provided with a wear-resistant CVD coating.

[0042] In yet another embodiment of the present invention, the cemented carbide substrate comprises several layers, suitably at least a carbonitride layer and an Al 2 O 3 The wear-resistant CVD coating includes a layer.

[0043] By cutting tool is meant herein an insert, an end mill or a drill.

[0044] The present invention also relates to a method for producing the above-mentioned cutting tool comprising a cemented carbide substrate as described above, the method comprising the steps of: - providing a powder forming a hard component comprising WC; - providing a powder containing Ni and Al forming a binder phase; - W and / or W, so that the eta phase is formed after sintering 2 Adding C to adjust the carbon content; - grinding the powder with a grinding liquid, drying the powder and pressing the powder into a green body; subjecting the green body to a sintering process; Including, The method further includes a carburizing step.

[0045] Here, the carburizing step means subjecting the green body or sintered cemented carbide to a high temperature carburizing atmosphere, which can be achieved by introducing any carbon-containing gas or gas mixture, such as CO, CH4, etc.

[0046] The carburizing step can be carried out either before, during or after the liquid phase sintering step, preferably at a temperature T liq and solidification temperature T sol It can be performed during the temperature interval between two temperatures T liq and T sol Both refer to the liquidus and solidus temperatures of the binder, i.e. not to the liquidus of WC. Preferably, the carburization step is carried out at a temperature between 1340 and 1430°C, more preferably between 1350 and 1420°C. The ... 4 (or mixtures thereof) to introduce a carbon-rich atmosphere. 2 Other protective gases that do not participate in the carburization process, such as Ar, can also be introduced along with the carbon gas source. Typical carburization (CO) partial pressures can range between 50 and 900 mbar depending on the desired gradient thickness. The duration of the carburization process is suitably between 15 minutes and 4 hours, preferably between 40 minutes and 3 hours. Duration, as used herein, refers to the period of time during which a carburizing environment is present and the temperature exceeds the solidification temperature T sol This means a time exceeding

[0047] Depending on the desired gradient thickness, the partial pressure of the carbon-containing gas and / or the duration of the carburization step may need to be adjusted.

[0048] In one embodiment of the present invention, the carburizing step is part of a sintering cycle, which means herein the sintering of the green body into a sintered hardmetal body, which is carried out by including a liquid sintering step.

[0049] In one embodiment of the present invention, the carburization step is performed after the liquidus step of the sintering process. A carbon-containing gas is then introduced during the cooling step. Within the desired temperature range (between the solidus and liquidus temperatures of the binder), the cooling rate is adjusted to control the diffusion and transport processes, and thus the eta-phase dissolution rate, binder transport and gradient thickness. The carbon activity, adjusted by the carbon partial pressure at the surface of the cemented carbide during the carburization process, also controls the rate of transformation and gradient formation.

[0050] In one embodiment of the present invention, the carburizing step is carried out in a separate sintering process, and then the already sintered hard-metal produced according to the process described above but without the carburizing step is introduced into a sintering furnace and subjected to a second sintering process including the carburizing step as described above.

[0051] For example, W or W 2 When adjusting the amount of eta phase, which is done by adjusting the carbon balance to a lower carbon content by adding C, it is left to the skilled person to determine the correct raw material composition to obtain the desired amount of eta phase after sintering. To a certain extent, the desired carbon content can be estimated or calculated from the phase diagram of the particular cemented carbide composition. However, it is also well known that a certain amount of carbon is lost during sintering due to the presence of oxygen, which reacts with carbon. Therefore, a certain excess of carbon must be present to compensate for this loss. How much carbon is lost during sintering depends on many things, for example, the type of furnace, the oxygen content in the raw material, etc.

[0052] The raw materials containing Ni and Al which form the binder phase can be added as pure metals, alloys of two or more metals, or their carbides, nitrides or carbonitrides. The raw materials should be added in amounts such that the binder phase after sintering has the above composition.

[0053] The powder forming the hard component contains WC and has an average particle size of preferably 0.2 to 10 μm, more preferably 0.4 to 5 μm.

[0054] Any liquid commonly used as a grinding liquid in conventional cemented carbide manufacturing can be used. The grinding liquid is preferably one or more of water, alcohol, or organic solvent. Other compounds commonly known in the art, such as dispersants, pH adjusters, etc., can also be added to the slurry. Organic binders, such as paraffin, polyethylene glycol (PEG), long chain fatty acids, etc., also function as pressurizing agents in some cases.

[0055] The raw powder and grinding liquid are then subjected to a grinding operation in a suitable mill, such as, for example, a ball mill or an attritor mill.

[0056] The milled slurry is then dried by spray drying to form agglomerated granules. In small scale experiments, other drying methods, such as pan drying, can also be used.

[0057] The dried powder / granules are then formed into a green body by pressing operations such as uniaxial pressing, multiaxial pressing, etc.

[0058] The green body formed from the powder / granules produced according to the present invention is then sintered according to any conventional sintering method, such as vacuum sintering, sinter-HIP, gas pressure sintering (GPS), and the like.

[0059] Sintering is preferably carried out at the liquidus temperature, the exact temperature depending on the exact composition of the binder.

[0060] In one embodiment of the present invention, the sintering temperature is between 1350 and 1550°C.

[0061] In one embodiment of the present invention, a coating is provided on a cemented carbide substrate.

[0062] In one embodiment of the present invention, the cemented carbide substrate manufactured as described above is provided with a wear resistant coating as described above using CVD or PVD techniques.

[0063] The coating may also be subjected to additional treatments such as brushing, blasting treatments, etc.

[0064] The present invention also discloses a cemented carbide cutting tool manufactured according to the above-mentioned method. EXAMPLES

[0065] Example 1 The cemented carbide is manufactured by providing the raw materials according to Table 1. The average particle size of the WC powder was 1.42 μm. The powder is mixed with a grinding liquid of ethanol / water and polyethylene glycol. The slurry is then ground, dried and subsequently pressed into a green body. The green body is then placed in a sintering furnace and sintered at 1500° C. for 1 hour (liquid phase sintering).

[0066] The sintered pieces were then subjected to a second sintering process in which a liquid phase sintering step was carried out at 1430 °C, during which a carburizing atmosphere was created using a CO partial pressure of 200 mBar. The duration of the carburizing step was 120 minutes. They were then cooled to room temperature in the furnace. TIFF0007689529000001.tif22170

[0067] The microstructure of the sintered cemented carbide was then investigated. First, a cross section was provided and the cemented carbide was etched for 1 second using 10% Murakami solution. The thickness of the gradient surface zone free of eta phase was measured on 500x LOM images (see Figure 1). The volume % eta phase in the inner part was also measured using image analysis of the LOM images with the software Image J.

[0068] The presence and size of γ' precipitates were measured on the SEM images. The precipitates were present in both the inner part (bulk) and the gradient surface zone. In Figure 2, the γ' precipitates in the binder can be seen in the inner part of the cemented carbide. It was also observed that the size of the precipitates in the gradient surface zone was smaller than that in the inner part of the cemented carbide. The size of the γ' precipitates was done manually using the average linear intercept method. TIFF0007689529000002.tif26170

Claims

1. A cutting tool comprising a cemented carbide substrate containing tungsten carbide and 3-20 wt. % of a binder, the binder being an intermetallic compound y'-Ni embedded in a substitutional solid solution matrix containing Al and Ni with a weight ratio Al / Ni between 0.02 and 0.

15. ３ %。 A cutting tool comprising: a binder having a total amount of Ni and Al-precipitates, the total amount of Ni and Al being between 70 and 95 weight % of the binder; the cemented carbide comprising an inner portion and a gradient surface zone having a depth between 5 and 400 μm, the inner portion comprising eta phase in an amount such that the volume fraction of eta phase is between 1 and 30 volume %, the gradient surface zone being eta phase free.

2. Intermetallic compound y'-Ni ３ 2. The cutting tool of claim 1, wherein the average grain size of the Al-precipitates is between 10 and 1000 nm.

3. Intermetallic compound y'-Ni ３ A cutting tool according to any of claims 1 or 2, wherein the average grain size of the Al-precipitates is between 10 and 500 nm.

4. Intermetallic compound y'-Ni ３ A cutting tool according to any of claims 1 to 3, wherein the average grain size of the Al-precipitates is smaller in the gradient surface zone than in the inner part of the cemented carbide.

5. A cutting tool according to any of the preceding claims, wherein the weight ratio between Al / Ni is suitably between 0.03 and 0.

07.

6. A cutting tool according to any of claims 1 to 5, wherein the total amount of Ni and Al is between 80 and 95% by weight of the bond.

7. 7. A cutting tool according to any of the preceding claims, wherein the amount of eta phase in the inner portion of the cemented carbide is between 3 and 10 volume %.

8. A cutting tool according to any of the preceding claims, wherein the binder content in the surface zone is lower than in the inner portion of the cemented carbide.

9. The cutting tool according to claim 1 , wherein the cemented carbide is essentially free of Co.

10. 10. The cutting tool according to claim 1, wherein the cemented carbide is essentially free of Mo.

11. - Providing a powder forming a hard component comprising WC; - providing a powder containing Ni and Al forming a binder phase; - W and / or W, so that the eta phase is formed after sintering ２ Adding C to adjust the carbon content; - grinding said powder with a grinding liquid, drying said powder and pressing said powder into a green body; - subjecting the green body to a sintering step; A method for manufacturing a cutting tool according to any one of claims 1 to 10, comprising: - The method further comprising a carburization step.

12. The temperature of the carburizing process is the temperature T ｌｉｑ and the solidification temperature T of the binder ｓｏｌ The method for producing a cutting tool according to claim 11, wherein

13. The gas during the carburizing process is CO or CH ４ The method for producing a cutting tool according to claim 11 or 12,

14. A method for manufacturing a cutting tool according to any of claims 11 to 13, wherein the temperature of the carburizing step is between 1340 and 1430°C and the duration of the carburizing step is between 15 minutes and 4 hours.

15. A method for manufacturing a cutting tool according to any of claims 11 to 14, wherein the cutting tool is provided with a wear resistant CVD or PVD coating.

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