US20070175103A1 - Method of making a tool component - Google Patents
Method of making a tool component Download PDFInfo
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- US20070175103A1 US20070175103A1 US10/558,239 US55823904A US2007175103A1 US 20070175103 A1 US20070175103 A1 US 20070175103A1 US 55823904 A US55823904 A US 55823904A US 2007175103 A1 US2007175103 A1 US 2007175103A1
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- abrasive
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- diamond
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- C—CHEMISTRY; METALLURGY
- C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
- C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
- C04B35/00—Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products
- C04B35/515—Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products based on non-oxide ceramics
- C04B35/56—Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products based on non-oxide ceramics based on carbides or oxycarbides
- C04B35/5607—Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products based on non-oxide ceramics based on carbides or oxycarbides based on refractory metal carbides
- C04B35/5626—Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products based on non-oxide ceramics based on carbides or oxycarbides based on refractory metal carbides based on tungsten carbides
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B22—CASTING; POWDER METALLURGY
- B22F—WORKING METALLIC POWDER; MANUFACTURE OF ARTICLES FROM METALLIC POWDER; MAKING METALLIC POWDER; APPARATUS OR DEVICES SPECIALLY ADAPTED FOR METALLIC POWDER
- B22F7/00—Manufacture of composite layers, workpieces, or articles, comprising metallic powder, by sintering the powder, with or without compacting wherein at least one part is obtained by sintering or compression
- B22F7/02—Manufacture of composite layers, workpieces, or articles, comprising metallic powder, by sintering the powder, with or without compacting wherein at least one part is obtained by sintering or compression of composite layers
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B24—GRINDING; POLISHING
- B24D—TOOLS FOR GRINDING, BUFFING OR SHARPENING
- B24D18/00—Manufacture of grinding tools or other grinding devices, e.g. wheels, not otherwise provided for
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B24—GRINDING; POLISHING
- B24D—TOOLS FOR GRINDING, BUFFING OR SHARPENING
- B24D3/00—Physical features of abrasive bodies, or sheets, e.g. abrasive surfaces of special nature; Abrasive bodies or sheets characterised by their constituents
- B24D3/02—Physical features of abrasive bodies, or sheets, e.g. abrasive surfaces of special nature; Abrasive bodies or sheets characterised by their constituents the constituent being used as bonding agent
- B24D3/04—Physical features of abrasive bodies, or sheets, e.g. abrasive surfaces of special nature; Abrasive bodies or sheets characterised by their constituents the constituent being used as bonding agent and being essentially inorganic
- B24D3/06—Physical features of abrasive bodies, or sheets, e.g. abrasive surfaces of special nature; Abrasive bodies or sheets characterised by their constituents the constituent being used as bonding agent and being essentially inorganic metallic or mixture of metals with ceramic materials, e.g. hard metals, "cermets", cements
- B24D3/10—Physical features of abrasive bodies, or sheets, e.g. abrasive surfaces of special nature; Abrasive bodies or sheets characterised by their constituents the constituent being used as bonding agent and being essentially inorganic metallic or mixture of metals with ceramic materials, e.g. hard metals, "cermets", cements for porous or cellular structure, e.g. for use with diamonds as abrasives
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- C04B35/00—Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products
- C04B35/515—Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products based on non-oxide ceramics
- C04B35/52—Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products based on non-oxide ceramics based on carbon, e.g. graphite
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- C—CHEMISTRY; METALLURGY
- C23—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
- C23C—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
- C23C24/00—Coating starting from inorganic powder
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- C—CHEMISTRY; METALLURGY
- C23—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
- C23C—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
- C23C24/00—Coating starting from inorganic powder
- C23C24/08—Coating starting from inorganic powder by application of heat or pressure and heat
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- C—CHEMISTRY; METALLURGY
- C23—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
- C23C—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
- C23C30/00—Coating with metallic material characterised only by the composition of the metallic material, i.e. not characterised by the coating process
- C23C30/005—Coating with metallic material characterised only by the composition of the metallic material, i.e. not characterised by the coating process on hard metal substrates
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- C—CHEMISTRY; METALLURGY
- C23—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
- C23C—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
- C23C4/00—Coating by spraying the coating material in the molten state, e.g. by flame, plasma or electric discharge
- C23C4/18—After-treatment
- C23C4/185—Separation of the coating from the substrate
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- C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
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- C04B2235/00—Aspects relating to ceramic starting mixtures or sintered ceramic products
- C04B2235/02—Composition of constituents of the starting material or of secondary phases of the final product
- C04B2235/30—Constituents and secondary phases not being of a fibrous nature
- C04B2235/38—Non-oxide ceramic constituents or additives
- C04B2235/3817—Carbides
- C04B2235/3839—Refractory metal carbides
- C04B2235/3847—Tungsten carbides
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- C—CHEMISTRY; METALLURGY
- C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
- C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
- C04B2235/00—Aspects relating to ceramic starting mixtures or sintered ceramic products
- C04B2235/02—Composition of constituents of the starting material or of secondary phases of the final product
- C04B2235/30—Constituents and secondary phases not being of a fibrous nature
- C04B2235/40—Metallic constituents or additives not added as binding phase
- C04B2235/405—Iron group metals
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- C—CHEMISTRY; METALLURGY
- C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
- C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
- C04B2235/00—Aspects relating to ceramic starting mixtures or sintered ceramic products
- C04B2235/02—Composition of constituents of the starting material or of secondary phases of the final product
- C04B2235/30—Constituents and secondary phases not being of a fibrous nature
- C04B2235/42—Non metallic elements added as constituents or additives, e.g. sulfur, phosphor, selenium or tellurium
- C04B2235/422—Carbon
- C04B2235/427—Diamond
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- C—CHEMISTRY; METALLURGY
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- C04B2235/00—Aspects relating to ceramic starting mixtures or sintered ceramic products
- C04B2235/02—Composition of constituents of the starting material or of secondary phases of the final product
- C04B2235/50—Constituents or additives of the starting mixture chosen for their shape or used because of their shape or their physical appearance
- C04B2235/54—Particle size related information
- C04B2235/5418—Particle size related information expressed by the size of the particles or aggregates thereof
- C04B2235/5436—Particle size related information expressed by the size of the particles or aggregates thereof micrometer sized, i.e. from 1 to 100 micron
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- C04B2235/00—Aspects relating to ceramic starting mixtures or sintered ceramic products
- C04B2235/65—Aspects relating to heat treatments of ceramic bodies such as green ceramics or pre-sintered ceramics, e.g. burning, sintering or melting processes
- C04B2235/658—Atmosphere during thermal treatment
- C04B2235/6582—Hydrogen containing atmosphere
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- C04B2235/00—Aspects relating to ceramic starting mixtures or sintered ceramic products
- C04B2235/70—Aspects relating to sintered or melt-casted ceramic products
- C04B2235/74—Physical characteristics
- C04B2235/75—Products with a concentration gradient
Definitions
- Abrasive compacts are used extensively in cutting, milling, grinding, drilling, boring and other abrasive operations.
- Abrasive compacts consist of a mass of diamond or cubic boron nitride particles bonded into a coherent, polycrystalline conglomerate.
- the abrasive particle content of abrasive compacts is high and there is generally an extensive amount of direct particle-to-particle bonding.
- Abrasive compacts are made under elevated temperature and pressure conditions at which the abrasive particle, be it diamond or cubic boron nitride, is crystallographically stable.
- Cemented carbide is used as a material for producing tool components which have an abrasiveness and hardness less than PCD or PCBN.
- Such tool components may consist of a homogeneous cemented carbide or a cemented carbide which varies in composition.
- the material of one source comprises a mass of discrete ultra-hard abrasive particles such as diamond or cubic boron nitride in a binder.
- the material of the other source comprises a mass of discrete abrasive particles different to those of the material of the first source, for example carbide particles, in a binder.
- the materials of the two sources contain the same abrasive particle, but in different particle sizes.
- the materials of the two sources contain the same abrasive particle, but in different particle sizes.
- the mixed materials are delivered from the mixing zone in the form of a spray.
- the surface to which the layer or layers of mixed material is applied may be the surface of a cemented carbide substrate producing, for example, a green state composite abrasive compact.
- This green state composite abrasive compact on sintering at temperature and pressure conditions at which the abrasive particle is crystallographically stable, results in a composite abrasive compact being produced.
- the surface to which the layer of mixed materials is applied may be the surface of a substrate which is sacrificed leaving a green state layer or layers of mixed materials which may be sintered.
- apparatus comprising containers 10 , 12 .
- the containers are suitable for holding a mass of abrasive particles in a suitable binder.
- suitable binders are organic binders such as methyl or ethyl cellulose or polyvinylpyrrolidone.
- the abrasive particles will generally be uniformly dispersed in the binder and will be flowable.
- the abrasive particles of container 10 will, for example, be ultra-hard abrasive particles such as diamond or cubic boron nitride.
- the abrasive particles of container 12 will be different to those of container 10 and will, for example, be carbide particles.
- Passage 14 from container 10 leads to a mixing zone 16 . Flow of material from the container 10 is controlled from valve 18 .
- Passage 20 from container 12 leads to the mixing zone 16 .
- Flow of material from container 12 is controlled by valve 22 .
- the method of the invention it is possible to produce layered structures having a wide range of compositions varying from each other. Further, the illustrated embodiment has the layers one on top of the other. The method can also be used to produce layers which are vertically or otherwise disposed relative to each other.
- the layered structure may be applied directly to a substrate to which it is desired to bond the layers on sintering.
- the layers may be applied to a surface, then removed from that surface and applied to a surface of a substrate to which bonding takes place.
- a cylindrical-shaped component was prepared with a WC/diamond gradient in the axial direction using the wet powder spraying (WPS) method of the invention.
- the starting layer of the cylinder was a 4 mm layer of WC/Co. This was not prepared using the wet powder spraying method, but was rather pressed from commercially available powder at 100 MPa to obtain a strong, porous support for the subsequent layer deposition.
- This base layer was then strengthened further by a pre-sintering treatment under hydrogen at 600° C. The porosity of this layer was chosen to achieve a similar shrinkage behaviour to the overlying layers.
- the WC/Co grain composition was the same as that used in the diamond graded layers.
- the green compact was then de-binded at a sufficiently high temperature to remove the binder and dispersant phases.
- a high pressure, high temperature treatment was then used to sinter the green compact to produce a sintered compact.
- the sintered compact exhibited a marked reduction in residual tensile stresses in the abrasive compact layer.
- a cylindrical-shaped component was prepared with a diamond grain size gradient in the axial direction using a wet powder spraying (WPS) method similar to that described in Example 1.
- the diamond layer immediately adjacent to the WC/Co base layer was chosen to have an average grain size of approximately 25 ⁇ m, whilst the diamond layer in the uppermost layer was chosen to have an average grain size of approximately 4 ⁇ m.
- 50 layers were deposited, each of approximately 100 ⁇ m in thickness. The ratio of the two diamond grain sizes was altered in monotonic manner in 2% compositional intervals, from 100% 25 ⁇ m diamond at the base surface to 100% 4 ⁇ m diamond at the uppermost surface.
- the mass composition of the WPS suspension did not alter signficantly from the base to the top layers, as the matrix material was consistently diamond throughout.
- the final compact was de-binded in a similar fashion to the compact generated in Example 1, and was then treated under high pressure and high temperature to achieve a fully sintered compact with diamond to diamond bonding.
- the sintered compact once again provided an abrasive compact layer with a significant reduction in residual tensile stresses.
- a cylindrical-shaped component was prepared with a gradient in diamond grain size and chemical composition in the axial direction using a wet powder spraying (WPS) method similar to that described in Example 1.
- WPS wet powder spraying
- the layer immediately adjacent to the WC/Co base layer contained diamond grains of 25 ⁇ m in size and WC/Co particles of 2.5 ⁇ m in size in a 75:25 (diamond:WC/Co) mass ratio.
- the uppermost layer contained 100% diamond material of an average of 4 ⁇ m in size. The ratio of these two source compositions was altered in monotonic manner in 2% compositional intervals, from 100% (25 ⁇ m diamond/(WC/Co) mix) at the base surface to 100% 4 ⁇ m diamond at the uppermost surface.
- the final compact was then de-binded in a similar fashion to the compact generated in Example 1, and was then treated under high pressure and high temperature to achieve a fully sintered compact with diamond to diamond bonding. Residual tensile stresses were once again significantly reduced in the abrasive compact layer.
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Abstract
A method of producing a tool component comprising a working portion of bonded abrasive particles including a non-homogeneous region. The method includes the step of providing at least two sources of a material comprising abrasive particles in a suitable binder, the materials of the sources differing from each other. The material of one source may comprise diamond or cubic boron nitride particles, whilst the material of the other source may comprise carbide particles. Alternatively, the materials of the two sources may contain the same abrasive particle, such as diamond or cubic boron nitride particles, but in different particle sizes. The materials are delivered to a zone where mixing occurs, and the mixture is applied to a surface to produce a layer of the mixed materials on the surface, typically by spraying. By controlling the quantity of material from each source which is delivered to the mixing zone, different mixtures of the two abrasives can be created. In this way, layers, e.g. one on top of the other, can be produced which differ from their neighbours in abrasive particle composition. These layers, on sintering, form non-homogeneous regions in the working portion of a tool component.
Description
- This invention relates to a method of making a tool component.
- Abrasive compacts are used extensively in cutting, milling, grinding, drilling, boring and other abrasive operations. Abrasive compacts consist of a mass of diamond or cubic boron nitride particles bonded into a coherent, polycrystalline conglomerate. The abrasive particle content of abrasive compacts is high and there is generally an extensive amount of direct particle-to-particle bonding. Abrasive compacts are made under elevated temperature and pressure conditions at which the abrasive particle, be it diamond or cubic boron nitride, is crystallographically stable.
- Diamond abrasive compacts are also known as polycrystalline diamond or PCD and cubic boron nitride abrasive compacts are also known as polycrystalline CBN or PCBN.
- Abrasive compacts tend to be brittle and in use they are frequently supported by being bonded to a cemented carbide substrate or support. Such supported abrasive compacts are known in the art as composite abrasive compacts. Composite abrasive compacts may be used as such in a working surface of an abrasive tool. Where the composite abrasive compact has a thick abrasive compact layer, particularly a thick diamond compact layer, residual tensile stresses in the abrasive compact layer develop giving rise to problems in use. These stresses contribute to delamination and fracture of the compact layer in use. To minimise these problems, the interface between the abrasive compact layer and carbide substrate may be profiled and/or the composition of the compact layer varied, for example by introducing some carbide particle content in a region or regions adjacent the substrate/compact layer interface.
- Cemented carbide is used as a material for producing tool components which have an abrasiveness and hardness less than PCD or PCBN. Such tool components may consist of a homogeneous cemented carbide or a cemented carbide which varies in composition.
- According to the present invention, a method of producing a tool component which comprises a working portion of bonded abrasive particles and which includes a non-homogeneous region includes the steps of providing at least two sources of a material comprising abrasive particles in a suitable binder, the materials of the sources differing from each other, delivering a quantity of the materials to a zone where mixing occurs and applying the mixed materials to a surface to produce a layer of the mixed materials on the surface. The layer of mixed materials will form at least a part of the non-homogeneous region of the working portion of the tool component. The non-homogeneous region can differ in size of abrasive particle, in the nature of the abrasive particle or in a combination thereof. The layer of the mixed materials is a green state form of the non-homogeneous region.
- In one form of the invention, the material of one source comprises a mass of discrete ultra-hard abrasive particles such as diamond or cubic boron nitride in a binder. The material of the other source comprises a mass of discrete abrasive particles different to those of the material of the first source, for example carbide particles, in a binder. By controlling the quantity of material from each source which is delivered to the mixing zone, different mixtures of the two abrasives can be created. In this way, layers, e.g. one on top of the other, can be produced which differ from their neighbours in abrasive particle composition. These layers, on sintering, form non-homogeneous regions in the working portion of a tool component.
- In another form of the invention, the materials of the two sources contain the same abrasive particle, but in different particle sizes. In a similar manner by controlling the quantity of material from each source which is. delivered to the mixing zone, layers which differ in particle size composition from each other can be produced.
- It is preferred that the mixed materials are delivered from the mixing zone in the form of a spray.
- The surface to which the layer or layers of mixed material is applied may be the surface of a cemented carbide substrate producing, for example, a green state composite abrasive compact. This green state composite abrasive compact, on sintering at temperature and pressure conditions at which the abrasive particle is crystallographically stable, results in a composite abrasive compact being produced. The surface to which the layer of mixed materials is applied may be the surface of a substrate which is sacrificed leaving a green state layer or layers of mixed materials which may be sintered.
- The invention will now be described in more detail, by way of example only, with reference to the accompanying drawing which is a diagrammatical representation of apparatus suitable for carrying out an embodiment of the invention.
- Embodiments of the invention will now be described with reference to the accompanying drawing. Referring to the drawing, there is shown
10, 12. The containers are suitable for holding a mass of abrasive particles in a suitable binder. Examples of suitable binders are organic binders such as methyl or ethyl cellulose or polyvinylpyrrolidone. The abrasive particles will generally be uniformly dispersed in the binder and will be flowable. The abrasive particles ofapparatus comprising containers container 10 will, for example, be ultra-hard abrasive particles such as diamond or cubic boron nitride. The abrasive particles ofcontainer 12 will be different to those ofcontainer 10 and will, for example, be carbide particles.Passage 14 fromcontainer 10 leads to a mixing zone 16. Flow of material from thecontainer 10 is controlled from valve 18.Passage 20 fromcontainer 12 leads to the mixing zone 16. Flow of material fromcontainer 12 is controlled byvalve 22. - In use, a
substrate 24, typically a cemented carbide substrate, is provided. The substrate is cylindrical in shape and has an upperflat surface 26 and a lowerflat surface 28. Afirst layer 30 of mixed materials is applied to thesurface 26. This is achieved byopening valves 18, 22 to a desired extent, thereby delivering material from each of the 10, 12 to the mixing zone 16. The materials are thoroughly mixed in zone 16 and thereafter sprayed throughcontainers nozzle 32 on to thesurface 26. Thereafter, asecond layer 34 is applied to thelayer 30. This layer will also be applied using this wet powder spraying (WPS) method, save that the proportions of material delivered from 10 and 12 will be varied by means of the amount delivered through thecontainers valves 18, 22. Additional layers are added to thelayer 34. The compositions of these additional layers will be tailored to meet specific requirements. - The layered product is a green state product. The layers on the
substrate 34 are all coherent and hold their shape. The green state product is then sintered to cause the various layers to sinter and bond to each other and thelayer 30 to bond to the substrate. For example, thecontainer 10 may contain diamond particles, in which event the container will generally contain finely particulate metal such as nickel, iron or cobalt as a mixture with the diamond particles. Thecontainer 12 may contain carbide particles. The 30 and 34 will generally contain a mixture of diamond particles and carbide particles in varying amounts. The outer layer or layers will generally contain only diamond particles. The green state product will be sintered under diamond synthesis conditions and the resulting product will be a composite diamond abrasive compact. A diamond compact layer will be formed from the green state layers. The diamond compact layer of such a product will be substantially stress-free.layers - In an alternative embodiment of the invention, the
container 10 may contain abrasive particles of a particular size and thecontainer 12 contain the same abrasive particles but of different size. The various layers in the green state product may thus all contain the same abrasive particles but the size composition of each layer may be varied to achieve a particular objective. - It will be appreciated that by use of the method of the invention, it is possible to produce layered structures having a wide range of compositions varying from each other. Further, the illustrated embodiment has the layers one on top of the other. The method can also be used to produce layers which are vertically or otherwise disposed relative to each other.
- The layered structure may be applied directly to a substrate to which it is desired to bond the layers on sintering. Alternatively, the layers may be applied to a surface, then removed from that surface and applied to a surface of a substrate to which bonding takes place.
- The method of the invention may be further understood with reference to the following non-limiting Examples.
- A cylindrical-shaped component was prepared with a WC/diamond gradient in the axial direction using the wet powder spraying (WPS) method of the invention. The starting layer of the cylinder was a 4 mm layer of WC/Co. This was not prepared using the wet powder spraying method, but was rather pressed from commercially available powder at 100 MPa to obtain a strong, porous support for the subsequent layer deposition. This base layer was then strengthened further by a pre-sintering treatment under hydrogen at 600° C. The porosity of this layer was chosen to achieve a similar shrinkage behaviour to the overlying layers. The WC/Co grain composition was the same as that used in the diamond graded layers.
- 49 gradient layers, each of approximately 100 μm thickness, with WC/diamond ratios varying in a monotonic manner were then deposited onto the WC/Co base by the WPS method. The diamond and WC particles were provided from separate containers, each in a suspension which included polyvinylpyrrolidone as binder, Lupasol P as dispersant and water. The composition ranged from 98% WC/2% diamond (by mass) in the layer immediately adjacent to the base layer to 100% diamond in the uppermost layer. The composition was altered in 2% steps by altering the flow of WC particles from one container and diamond particles from another container. In order to preserve a cylindrical shape in the component, a cylindrical mold was used for containing the sprayed layers.
- As the concentration of diamond particles, which had an average particle size of about 4 μm, in the suspension increased (according to the axial gradient), so the overall composition of the suspension altered. The decrease in matrix mass due to the density difference between diamond and WC/Co meant that the binder and dispersant masses had to decrease in a similar fashion. The overall water content therefore increased with respect to the dry powder weight. Each layer was dried before the subsequent layer was sprayed to prevent shrinkage problems.
- The green compact was then de-binded at a sufficiently high temperature to remove the binder and dispersant phases. A high pressure, high temperature treatment was then used to sinter the green compact to produce a sintered compact. The sintered compact exhibited a marked reduction in residual tensile stresses in the abrasive compact layer.
- A cylindrical-shaped component was prepared with a diamond grain size gradient in the axial direction using a wet powder spraying (WPS) method similar to that described in Example 1. The diamond layer immediately adjacent to the WC/Co base layer was chosen to have an average grain size of approximately 25 μm, whilst the diamond layer in the uppermost layer was chosen to have an average grain size of approximately 4 μm. 50 layers were deposited, each of approximately 100 μm in thickness. The ratio of the two diamond grain sizes was altered in monotonic manner in 2% compositional intervals, from 100% 25 μm diamond at the base surface to 100% 4 μm diamond at the uppermost surface.
- The mass composition of the WPS suspension did not alter signficantly from the base to the top layers, as the matrix material was consistently diamond throughout. The final compact was de-binded in a similar fashion to the compact generated in Example 1, and was then treated under high pressure and high temperature to achieve a fully sintered compact with diamond to diamond bonding. The sintered compact once again provided an abrasive compact layer with a significant reduction in residual tensile stresses.
- A cylindrical-shaped component was prepared with a gradient in diamond grain size and chemical composition in the axial direction using a wet powder spraying (WPS) method similar to that described in Example 1.
- The layer immediately adjacent to the WC/Co base layer contained diamond grains of 25 μm in size and WC/Co particles of 2.5 μm in size in a 75:25 (diamond:WC/Co) mass ratio. The uppermost layer contained 100% diamond material of an average of 4 μm in size. The ratio of these two source compositions was altered in monotonic manner in 2% compositional intervals, from 100% (25 μm diamond/(WC/Co) mix) at the base surface to 100% 4 μm diamond at the uppermost surface.
- The final compact was then de-binded in a similar fashion to the compact generated in Example 1, and was then treated under high pressure and high temperature to achieve a fully sintered compact with diamond to diamond bonding. Residual tensile stresses were once again significantly reduced in the abrasive compact layer.
Claims (11)
1. A method of producing a tool component comprising a working portion of bonded abrasive particles, which includes a non-homogeneous region, the method including the steps of providing at least two sources of a material comprising abrasive particles in a suitable binder, the materials of the sources differing from each other, delivering a quantity of the materials to a zone where mixing occurs and applying the mixed materials to a surface to produce a layer of the mixed materials on the surface.
2. A method according to claim 1 , wherein the layer of mixed materials forms at least a part of the non-homogeneous region of the working portion of the tool component.
3. A method according to claim 1 , wherein the non-homogeneous region differs in size of abrasive particle, in the nature of the abrasive particle or in a combination thereof.
4. A method according to claim 1 , wherein the layer of the mixed materials is a green state form of the non-homogeneous region.
5. A method according to claim 1 , comprising first and second sources of material, the first source comprising a mass of discrete ultra-hard abrasive particles in a binder and the second source comprising a mass of discrete abrasive particles, different to those of the material of the first source, in a binder.
6. A method according to claim 5 , wherein the first source of material comprises a mass of discrete diamond or cubic boron nitride particles in a binder and the second source of material comprises carbide particles in a binder.
7. A method according to claim 1 , comprising first and second sources of material, the materials of the two sources containing the same abrasive particle, but in different particle sizes.
8. A method according to claim 1 , wherein the mixed materials are delivered from the mixing zone in the form of a spray.
9. A method according to claim 1 , wherein the surface to which the layer or layers of mixed material is applied is the surface of a cemented carbide substrate producing a green state composite abrasive compact.
10. A method according to claim 1 , wherein the surface to which the layer or layers of mixed materials is applied is the surface of a substrate which is sacrificed leaving a green state layer or layers of mixed materials which may be sintered.
11-12. (canceled)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| ZA2003/3969 | 2003-05-22 | ||
| ZA200303969 | 2003-05-22 | ||
| PCT/IB2004/001630 WO2004103641A1 (en) | 2003-05-22 | 2004-05-20 | Method of making a tool component |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US20070175103A1 true US20070175103A1 (en) | 2007-08-02 |
Family
ID=33477334
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US10/558,239 Abandoned US20070175103A1 (en) | 2003-05-22 | 2004-05-20 | Method of making a tool component |
Country Status (7)
| Country | Link |
|---|---|
| US (1) | US20070175103A1 (en) |
| EP (1) | EP1635992B1 (en) |
| JP (1) | JP2007500288A (en) |
| AT (1) | ATE385214T1 (en) |
| DE (1) | DE602004011612T2 (en) |
| WO (1) | WO2004103641A1 (en) |
| ZA (1) | ZA200509347B (en) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP2529694A1 (en) * | 2011-05-31 | 2012-12-05 | Ivoclar Vivadent AG | Method for generative production of ceramic forms by means of 3D jet printing |
| WO2012166747A2 (en) | 2011-05-27 | 2012-12-06 | Nanomech Inc. | Multi-layer coating with cubic boron nitride particles |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US7497280B2 (en) * | 2005-01-27 | 2009-03-03 | Baker Hughes Incorporated | Abrasive-impregnated cutting structure having anisotropic wear resistance and drag bit including same |
| KR20150121728A (en) | 2007-01-26 | 2015-10-29 | 다이아몬드 이노베이션즈, 인크. | Graded drilling cutters |
Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US20040093989A1 (en) * | 2000-12-21 | 2004-05-20 | Robert Fries | Method of making a cutting tool |
Family Cites Families (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0111600A1 (en) * | 1982-12-13 | 1984-06-27 | Reed Rock Bit Company | Improvements in or relating to cutting tools |
| US6315065B1 (en) * | 1999-04-16 | 2001-11-13 | Smith International, Inc. | Drill bit inserts with interruption in gradient of properties |
-
2004
- 2004-05-20 AT AT04734060T patent/ATE385214T1/en not_active IP Right Cessation
- 2004-05-20 ZA ZA200509347A patent/ZA200509347B/en unknown
- 2004-05-20 WO PCT/IB2004/001630 patent/WO2004103641A1/en not_active Ceased
- 2004-05-20 DE DE602004011612T patent/DE602004011612T2/en not_active Expired - Fee Related
- 2004-05-20 EP EP04734060A patent/EP1635992B1/en not_active Expired - Lifetime
- 2004-05-20 JP JP2006530669A patent/JP2007500288A/en active Pending
- 2004-05-20 US US10/558,239 patent/US20070175103A1/en not_active Abandoned
Patent Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US20040093989A1 (en) * | 2000-12-21 | 2004-05-20 | Robert Fries | Method of making a cutting tool |
Cited By (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2012166747A2 (en) | 2011-05-27 | 2012-12-06 | Nanomech Inc. | Multi-layer coating with cubic boron nitride particles |
| WO2012166745A1 (en) * | 2011-05-27 | 2012-12-06 | Nanomech Inc. | Thick cubic boron nitride (cbn) layer and manufacturing process therefor |
| WO2012166747A3 (en) * | 2011-05-27 | 2014-05-08 | Nanomech Inc. | Multi-layer coating with cubic boron nitride particles |
| US20140215925A1 (en) * | 2011-05-27 | 2014-08-07 | Nanomech, Inc. | Thick Cubic Boron Nitride (cBN) Layer and Manufacturing Process Therefor |
| EP2714387A4 (en) * | 2011-05-27 | 2015-03-11 | Nanomech Inc | MULTILAYER COATING CONTAINING CUBIC BORON NITRIDE PARTICLES |
| US9821435B2 (en) * | 2011-05-27 | 2017-11-21 | Nanomech, Inc. | Thick cubic boron nitride (CBN) layer and manufacturing process therefor |
| US10639768B2 (en) | 2011-05-27 | 2020-05-05 | P&S Global Holdings Llc | Multi-layer coating with cubic boron nitride particles |
| EP2529694A1 (en) * | 2011-05-31 | 2012-12-05 | Ivoclar Vivadent AG | Method for generative production of ceramic forms by means of 3D jet printing |
Also Published As
| Publication number | Publication date |
|---|---|
| DE602004011612D1 (en) | 2008-03-20 |
| ZA200509347B (en) | 2007-03-28 |
| ATE385214T1 (en) | 2008-02-15 |
| EP1635992A1 (en) | 2006-03-22 |
| DE602004011612T2 (en) | 2009-02-19 |
| WO2004103641A1 (en) | 2004-12-02 |
| EP1635992B1 (en) | 2008-01-30 |
| JP2007500288A (en) | 2007-01-11 |
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