AU2010255345A1 - Polycrystalline diamond - Google Patents

Polycrystalline diamond Download PDF

Info

Publication number
AU2010255345A1
AU2010255345A1 AU2010255345A AU2010255345A AU2010255345A1 AU 2010255345 A1 AU2010255345 A1 AU 2010255345A1 AU 2010255345 A AU2010255345 A AU 2010255345A AU 2010255345 A AU2010255345 A AU 2010255345A AU 2010255345 A1 AU2010255345 A1 AU 2010255345A1
Authority
AU
Australia
Prior art keywords
diamond
pcd
percent
grains
microns
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Abandoned
Application number
AU2010255345A
Inventor
Kaveshini Naidoo
Thembinkosi Shabalala
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Element Six Abrasives SA
Original Assignee
Element Six Abrasives SA
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Element Six Abrasives SA filed Critical Element Six Abrasives SA
Publication of AU2010255345A1 publication Critical patent/AU2010255345A1/en
Assigned to ELEMENT SIX ABRASIVES S.A. reassignment ELEMENT SIX ABRASIVES S.A. Request for Assignment Assignors: ELEMENT SIX (PRODUCTION) (PTY) LTD
Abandoned legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C01INORGANIC CHEMISTRY
    • C01BNON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
    • C01B32/00Carbon; Compounds thereof
    • C01B32/25Diamond
    • CCHEMISTRY; METALLURGY
    • C04CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04BLIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B35/00Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products
    • C04B35/515Shaped 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
    • C04B35/52Shaped 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
    • CCHEMISTRY; METALLURGY
    • C04CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04BLIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B35/00Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products
    • C04B35/622Forming processes; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products
    • C04B35/626Preparing or treating the powders individually or as batches ; preparing or treating macroscopic reinforcing agents for ceramic products, e.g. fibres; mechanical aspects section B
    • C04B35/628Coating the powders or the macroscopic reinforcing agents
    • C04B35/62802Powder coating materials
    • C04B35/62842Metals
    • CCHEMISTRY; METALLURGY
    • C04CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04BLIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B35/00Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products
    • C04B35/622Forming processes; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products
    • C04B35/626Preparing or treating the powders individually or as batches ; preparing or treating macroscopic reinforcing agents for ceramic products, e.g. fibres; mechanical aspects section B
    • C04B35/628Coating the powders or the macroscopic reinforcing agents
    • C04B35/62886Coating the powders or the macroscopic reinforcing agents by wet chemical techniques
    • CCHEMISTRY; METALLURGY
    • C04CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04BLIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B35/00Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products
    • C04B35/622Forming processes; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products
    • C04B35/64Burning or sintering processes
    • C04B35/645Pressure sintering
    • C04B35/6455Hot isostatic pressing
    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22CALLOYS
    • C22C26/00Alloys containing diamond or cubic or wurtzitic boron nitride, fullerenes or carbon nanotubes
    • EFIXED CONSTRUCTIONS
    • E21EARTH OR ROCK DRILLING; MINING
    • E21BEARTH OR ROCK DRILLING; OBTAINING OIL, GAS, WATER, SOLUBLE OR MELTABLE MATERIALS OR A SLURRY OF MINERALS FROM WELLS
    • E21B10/00Drill bits
    • E21B10/46Drill bits characterised by wear resisting parts, e.g. diamond inserts
    • CCHEMISTRY; METALLURGY
    • C01INORGANIC CHEMISTRY
    • C01PINDEXING SCHEME RELATING TO STRUCTURAL AND PHYSICAL ASPECTS OF SOLID INORGANIC COMPOUNDS
    • C01P2004/00Particle morphology
    • C01P2004/51Particles with a specific particle size distribution
    • CCHEMISTRY; METALLURGY
    • C04CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04BLIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B2235/00Aspects relating to ceramic starting mixtures or sintered ceramic products
    • C04B2235/02Composition of constituents of the starting material or of secondary phases of the final product
    • C04B2235/30Constituents and secondary phases not being of a fibrous nature
    • C04B2235/38Non-oxide ceramic constituents or additives
    • C04B2235/3817Carbides
    • CCHEMISTRY; METALLURGY
    • C04CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04BLIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B2235/00Aspects relating to ceramic starting mixtures or sintered ceramic products
    • C04B2235/02Composition of constituents of the starting material or of secondary phases of the final product
    • C04B2235/30Constituents and secondary phases not being of a fibrous nature
    • C04B2235/38Non-oxide ceramic constituents or additives
    • C04B2235/3817Carbides
    • C04B2235/3839Refractory metal carbides
    • CCHEMISTRY; METALLURGY
    • C04CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04BLIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B2235/00Aspects relating to ceramic starting mixtures or sintered ceramic products
    • C04B2235/02Composition of constituents of the starting material or of secondary phases of the final product
    • C04B2235/30Constituents and secondary phases not being of a fibrous nature
    • C04B2235/38Non-oxide ceramic constituents or additives
    • C04B2235/3817Carbides
    • C04B2235/3839Refractory metal carbides
    • C04B2235/3843Titanium carbides
    • CCHEMISTRY; METALLURGY
    • C04CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04BLIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B2235/00Aspects relating to ceramic starting mixtures or sintered ceramic products
    • C04B2235/02Composition of constituents of the starting material or of secondary phases of the final product
    • C04B2235/30Constituents and secondary phases not being of a fibrous nature
    • C04B2235/40Metallic constituents or additives not added as binding phase
    • CCHEMISTRY; METALLURGY
    • C04CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04BLIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B2235/00Aspects relating to ceramic starting mixtures or sintered ceramic products
    • C04B2235/02Composition of constituents of the starting material or of secondary phases of the final product
    • C04B2235/30Constituents and secondary phases not being of a fibrous nature
    • C04B2235/40Metallic constituents or additives not added as binding phase
    • C04B2235/402Aluminium
    • CCHEMISTRY; METALLURGY
    • C04CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04BLIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B2235/00Aspects relating to ceramic starting mixtures or sintered ceramic products
    • C04B2235/02Composition of constituents of the starting material or of secondary phases of the final product
    • C04B2235/30Constituents and secondary phases not being of a fibrous nature
    • C04B2235/40Metallic constituents or additives not added as binding phase
    • C04B2235/404Refractory metals
    • CCHEMISTRY; METALLURGY
    • C04CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04BLIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B2235/00Aspects relating to ceramic starting mixtures or sintered ceramic products
    • C04B2235/02Composition of constituents of the starting material or of secondary phases of the final product
    • C04B2235/30Constituents and secondary phases not being of a fibrous nature
    • C04B2235/40Metallic constituents or additives not added as binding phase
    • C04B2235/405Iron group metals
    • CCHEMISTRY; METALLURGY
    • C04CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04BLIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B2235/00Aspects relating to ceramic starting mixtures or sintered ceramic products
    • C04B2235/02Composition of constituents of the starting material or of secondary phases of the final product
    • C04B2235/30Constituents and secondary phases not being of a fibrous nature
    • C04B2235/42Non metallic elements added as constituents or additives, e.g. sulfur, phosphor, selenium or tellurium
    • CCHEMISTRY; METALLURGY
    • C04CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04BLIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B2235/00Aspects relating to ceramic starting mixtures or sintered ceramic products
    • C04B2235/02Composition of constituents of the starting material or of secondary phases of the final product
    • C04B2235/30Constituents and secondary phases not being of a fibrous nature
    • C04B2235/42Non metallic elements added as constituents or additives, e.g. sulfur, phosphor, selenium or tellurium
    • C04B2235/422Carbon
    • C04B2235/427Diamond
    • CCHEMISTRY; METALLURGY
    • C04CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04BLIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B2235/00Aspects relating to ceramic starting mixtures or sintered ceramic products
    • C04B2235/02Composition of constituents of the starting material or of secondary phases of the final product
    • C04B2235/50Constituents or additives of the starting mixture chosen for their shape or used because of their shape or their physical appearance
    • C04B2235/54Particle size related information
    • C04B2235/5418Particle size related information expressed by the size of the particles or aggregates thereof
    • C04B2235/5436Particle size related information expressed by the size of the particles or aggregates thereof micrometer sized, i.e. from 1 to 100 micron
    • CCHEMISTRY; METALLURGY
    • C04CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04BLIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B2235/00Aspects relating to ceramic starting mixtures or sintered ceramic products
    • C04B2235/02Composition of constituents of the starting material or of secondary phases of the final product
    • C04B2235/50Constituents or additives of the starting mixture chosen for their shape or used because of their shape or their physical appearance
    • C04B2235/54Particle size related information
    • C04B2235/5418Particle size related information expressed by the size of the particles or aggregates thereof
    • C04B2235/5445Particle size related information expressed by the size of the particles or aggregates thereof submicron sized, i.e. from 0,1 to 1 micron
    • CCHEMISTRY; METALLURGY
    • C04CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04BLIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B2235/00Aspects relating to ceramic starting mixtures or sintered ceramic products
    • C04B2235/02Composition of constituents of the starting material or of secondary phases of the final product
    • C04B2235/50Constituents or additives of the starting mixture chosen for their shape or used because of their shape or their physical appearance
    • C04B2235/54Particle size related information
    • C04B2235/5463Particle size distributions
    • C04B2235/5472Bimodal, multi-modal or multi-fraction
    • CCHEMISTRY; METALLURGY
    • C04CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04BLIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B2235/00Aspects relating to ceramic starting mixtures or sintered ceramic products
    • C04B2235/70Aspects relating to sintered or melt-casted ceramic products
    • C04B2235/74Physical characteristics
    • C04B2235/75Products with a concentration gradient
    • CCHEMISTRY; METALLURGY
    • C04CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04BLIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B2235/00Aspects relating to ceramic starting mixtures or sintered ceramic products
    • C04B2235/70Aspects relating to sintered or melt-casted ceramic products
    • C04B2235/80Phases present in the sintered or melt-cast ceramic products other than the main phase
    • CCHEMISTRY; METALLURGY
    • C04CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04BLIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B2235/00Aspects relating to ceramic starting mixtures or sintered ceramic products
    • C04B2235/70Aspects relating to sintered or melt-casted ceramic products
    • C04B2235/80Phases present in the sintered or melt-cast ceramic products other than the main phase
    • C04B2235/85Intergranular or grain boundary phases
    • CCHEMISTRY; METALLURGY
    • C04CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04BLIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B2235/00Aspects relating to ceramic starting mixtures or sintered ceramic products
    • C04B2235/70Aspects relating to sintered or melt-casted ceramic products
    • C04B2235/95Products characterised by their size, e.g. microceramics
    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22CALLOYS
    • C22C26/00Alloys containing diamond or cubic or wurtzitic boron nitride, fullerenes or carbon nanotubes
    • C22C2026/008Alloys containing diamond or cubic or wurtzitic boron nitride, fullerenes or carbon nanotubes with additional metal compounds other than carbides, borides or nitrides
    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22CALLOYS
    • C22C2204/00End product comprising different layers, coatings or parts of cermet

Landscapes

  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Ceramic Engineering (AREA)
  • Manufacturing & Machinery (AREA)
  • Organic Chemistry (AREA)
  • Materials Engineering (AREA)
  • Structural Engineering (AREA)
  • Inorganic Chemistry (AREA)
  • Geology (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Mechanical Engineering (AREA)
  • Mining & Mineral Resources (AREA)
  • General Life Sciences & Earth Sciences (AREA)
  • Metallurgy (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Physics & Mathematics (AREA)
  • Environmental & Geological Engineering (AREA)
  • Fluid Mechanics (AREA)
  • Geochemistry & Mineralogy (AREA)
  • Carbon And Carbon Compounds (AREA)
  • Earth Drilling (AREA)

Abstract

A polycrystalline diamond (PCD) material 10 comprising at least 88 volume percent and at most 99 volume percent diamond grains 12, the mean diamond grain contiguity being greater than 60.5 percent. The PCD material 10 is particularly but not exclusively for use in boring into the earth.

Description

WO 2010/140108 PCT/IB2010/052418 1 POLYCRYSTALLINE DIAMOND S Field The invention relates to polycrystalline diamond (PCD) material, a method for 10 making same and tools comprising same, particularly but not exclusively for use in boring into the earth. Background 15 Polycrystalline diamond (PCD) material comprises a mass of inter-grown diamond grains and interstices between the diamond grains. PCD may be made by subjecting an aggregated mass of diamond grains to a high pressure and temperature in the presence of a sintering aid such as cobalt, which may promote the inter-growth of diamond grains. The sintering aid may also be 20 referred to as a catalyst material for diamond. Interstices within the sintered PCD material may be wholly or partially filled with residual catalyst material. PCD may be formed on a cobalt-cemented tungsten carbide substrate, which may provide a source of cobalt catalyst material for the PCD. 25 PCD material may be used in a wide variety of tools for cutting, machining, drilling or degrading hard or abrasive materials such as rock, metal, ceramics, composites and wood-containing materials. For example, tool inserts comprising PCD material are widely used within drill bits used for boring into the earth in the oil and gas drilling industry. In many of these applications, the 30 temperature of the PCD material may become elevated as it engages rock or other workpiece or body with high energy. Unfortunately, mechanical properties of PCD material such as abrasion resistance, hardness and strength tend to deteriorate at elevated temperatures, which may be promoted by the residual catalyst material within it.
WO 2010/140108 PCT/IB2010/052418 2 Akaishi at a. disclose in the M1aterial Science and Engineering A (1988), volume 05/106, numbers i and 2, pages 517 to 523, a weli-sintered diamond wnni a Tine-graned homogleneous m!crostructure, wnicn was synthesised at 5 7.7 GPn and 9 00n rnces centigrade whepn diamond nowder witk 1 tn 5 volume percent Co or Ni additive was used as the starting material. European patent publication number EP 1 931 594 discloses a method for producing a polycrystalline diamond (PCD) body with an arithmetic mean as 10 sintered grain size less than 1 micron, wherein the catalyst metal comprises an iron group metal such as cobalt and the sintering pressure is between about 2.0 GPa and 7.0 GPa. United States patent application publication number 2005/0133277 discloses 15 PCD made using a sintering pressure and temperature at 65 kbar and 1,400 degrees centigrade. There is a need for polycrystalline diamond material having enhanced abrasion resistance. 20 Summary An aspect of the invention provides a polycrystalline diamond (PCD) material comprising diamond grains having a mean diamond grain contiguity of greater 25 than about 60 percent, greater than 60.5 percent, at least about 61.5 percent or even at least about 65 percent. In some embodiments of the invention, the diamond grains have a mean diamond grain contiguity of at most about 80 percent or at most about 77 percent. In one embodiment of the invention, the mean diamond grain contiguity may be in the range from 60.5 percent to 30 about 77 percent, and in one embodiment, the mean diamond grain contiguity may be in the range from 61.5 percent to about 77 percent.
WO 2010/140108 PCT/IB2010/052418 3 In some embodiments of the invention, the standard deviation of the diamond grain contiguity imay be at most aboUL 4t percent contiguity, at most about 3 percent contiguity or at most about 2 percent contiguity. 5 in some embodiments of the invention, the volume of the PCD matenra' may be at least about 0.5 mm 2 , at least about 75 mm 2 , at least about 150 mm 2 or at least about 300 mm 2 In one embodiment of the invention, the diamond grains may have the size 10 distribution characteristic that at least about 50 percent of the grains have an average size of greater than about 5 microns. In some embodiments, at least about 15 percent or at least about 20 percent of the grains have an average size in the range from about 10 microns to about 15 microns. 15 In one embodiment of the invention, the PCD material may comprise diamond grains having a multi-modal size distribution. In some embodiments of the invention, the diamond grains may have an average size of greater than 0.5 microns or greater than 1 micron, and at most 20 about 60 microns, at most about 30 microns, at most about 20 microns, at most about 15 microns or at most about 7 microns. In some embodiments of the invention, the PCD material may comprise diamond grains having a mean size of at most about 15 microns, less than about 10 microns or at most about 8 microns. In some embodiments of the invention, the diamond grains may 25 have an average size in the range from about 0.5 microns to about 20 microns, in the range from about 0.5 microns to about 10 microns, or in the range from about 1 micron to about 7 microns. In some embodiments of the invention, the content of the diamond in the PCD 30 material may be at least about 88 volume percent, at least about 90 volume percent or at least about 91 volume percent of the PCD material. In one embodiment, the content of the diamond may be at most about 99 volume percent of the PCD material. In some embodiments of the invention, the diamond content of the PCD material may be in the range from about 88 WO 2010/140108 PCT/IB2010/052418 4 volume percent to about 99 volume percent, or in the range from about 90 volume percent to about 96 volume percent of the PCD material. in one emhodimen the POD material may corise catalyst material for 5 di!mndl andA in 1ne 4modMent, thje content of th atlstmteilo diamond may be at most about 9 volume percent of the PCD material. In one embodiment, the content of the catalyst material for diamond may be at least about 1 volume percent of the PCD material. In some embodiments of the invention, the PCD material may comprise catalyst material for diamond in the 10 range from about 1 volume percent to about 10 volume percent, in the range from about 1 volume percent to about 8 volume percent, or in the range from about I to about 4 volume percent of the PCD material. In some embodiments of the invention, the PCD may have an average 15 interstitial mean free path of at most about 1.5 microns, at most about 1.3 microns or at most about 1 micron. In some embodiments of the invention, the PCD may have an average interstitial mean free path of at least about 0.05 microns, at least about 0.1 micron, at least about 0.2 microns or at least about 0.5 microns. In some embodiments, the PCD may have an average 20 interstitial mean free path in the range from 0.05 micron to about 1.3 micron, in the range from about 0.1 micron to about 1 micron or in the range from about 0.5 micron to about 1 micron. In some embodiments of the invention, the standard deviation of the mean 25 free path may be in the range from about 0.05 microns to about 1.5 micron, or in the range from about 0.2 micron to about 1 micron. In some embodiments of the invention, the PCD material may have a mean interstitial size of at least about 0.5 micron, at least about 1 micron or at least 30 about 1.5 microns. In some embodiments of the invention, the PCD material may have a mean interstitial size of at most about 3 microns or at most about 4 microns. In some embodiments, the standard deviation of the size distribution may be at most about 3 microns, at most about 2 microns or even at most about 1 micron.
WO 2010/140108 PCT/IB2010/052418 5 in one embodIent ofL the inventIon, the POD material may include a filler material comprising a ternary carbide of the formula Mx M'y Cz, M being at least one element selected from the group consisting of the transition metals 5 nd the rare earth metls; A' being nn elenmrnt sete from thIen gron consisting of Al, Ga, In, Ge, Sn, Pb, TI, Mg, Zn and Cd; x being in the range from 2.5 to 5.0; y being in the range from 0.5 to 3.0; and z being in the range from 0.1 to 1.2; and the PCD comprising diamond grains having average size in the range from 0.5 microns to 10 microns. In some embodiments, M may 10 be selected from the group consisting of Co, Fe, Ni, Mn, Cr, Pd, Pt, V, Nb, Ta, Ti, Zr, Ce, Y, La and Sc. In one embodiment, x may be 3. In one embodiment, y may be 1. In some embodiments, the filler material may comprise at least about 30 15 volume percent or at least about 40 volume percent of ternary carbide material. In one embodiment, the filler material may comprise only ternary carbide material and one or more other inter-metallic compounds, such that no free or unbound M is present in the filler material. In some embodiments, the filler material may further comprise free or unreacted catalyst material or 20 further carbide formed with Cr, V, Nb, Ta and / or Ti, or both the free or unreacted catalyst material and the further carbide. In one embodiment, the filler material may comprise at least about 40 volume percent or at least about 50 volume percent tin-based inter-metallic or teary carbide. 25 In some embodiments of the invention, the PCD material may have an oxidation onset temperature of at least about 800 degrees centigrade, at least about 900 degrees centigrade or at least about 950 degree centigrade. PCD material according to the invention may be made by a method including 30 forming a plurality of diamond grains into an aggregated mass and subjecting the aggregated mass of diamond grains to a pressure treatment at a pressure of greater than 6.0 GPa, at least about 6.2 GPa or at least about 6.5 GPa in the presence of a metallic catalyst material for diamond at a temperature sufficiently high for the catalyst material to melt, and sintering the diamond WO 2010/140108 PCT/IB2010/052418 6 grains to form PCD material; the diamond grains in the aggregated mass Ia vi ng the siz e di stri I ution caratI tat at least 50 percent I th LI g ra I i n nave an average size or greater than about 5 microns. in some emnoiments, east about 15 percent or at !east about percent of the grains have an average size i-n therangem abou 1 to a0 1t S. In some embodiments of the invention, the pressure is at most about 8 GPa, lower than 7.7 GPa, at most about 7.5 GPa, at most about 7.2 GPa or at most about 7.0 GPa. This method is an aspect of the invention. 10 In one embodiment of the invention, the method may include introducing an additive material into the aggregated mass, the additive material containing at least one element selected from V, Ti, Mo, Zr, W, Ta, Hf, Si, Sn or Al. In some embodiments, the additive material may comprise a compound or particles containing at least one element selected from V, Ti, Mo, Zr, W, Ta, 15 Hf, Si, Sn or Al. In one embodiment of the invention, the method may include introducing into pores or interstices within the aggregated mass a metal other than the catalyst material for diamond. In one embodiment, the metal may not be a catalyst for 20 diamond. In one embodiment, the catalyst material may comprise Co and the metal may be Sn. In one embodiment of the method, the catalyst material may be a metallic catalyst material. In some embodiments of the invention, the catalyst material 25 may comprise Co, Fe, Ni, and Mn, or alloys including any of these. In some embodiments of the method, the PCD material may be sintered for a period in the range from about 1 minute to about 30 minutes, in the range from about 2 minutes to about 15 minutes, or in the range from about 2 30 minutes to about 10 minutes. In some embodiments of the method, the temperature may be in the range from about 1,400 degrees centigrade to about 2,300 degrees centigrade, in the range from about 1,400 degrees centigrade to about 2,000 degrees WO 2010/140108 PCT/IB2010/052418 7 centigrade, in the range from about 1,450 degrees centigrade to about 1,700 degrees centigrade, or i the rangefom about 1,450 degrees centigrade about 1,650 degrees centigrade. 5 In come embodiments f the invention, the method may include subjering the PCD material to a heat treatment at a temperature of at least about 500 degrees centigrade, at least about 600 degrees centigrade or at least about 650 degrees centigrade for at least about 30 minutes. In some embodiments, the temperature may be at most about 850 degrees centigrade, at most about 10 800 degrees centigrade or at most about 750 degrees centigrade. In some embodiments, the PCD body may be subjected to the heat treatment for at most about 120 minutes or at most about 60 minutes. In one embodiment, the PCD body may be subjected to the heat treatment in a vacuum. 15 Embodiments of the method of the invention include subjecting the PCD material to a further pressure treatment at a pressure of at least about 2 GPa, at least about 5 GPa or even at Least about 6 GPa. In some embodiments, the further pressure treatment may be applied for a period of at least about 10 seconds or at least about 30 seconds. In one embodiment, the further 20 pressure treatment may be applied for a period of at most about 20 minutes. In one embodiment of the invention, the method may include removing metallic catalyst material for diamond from interstices between the diamond grains of the PCD material. 25 An embodiment of the invention provides a PCD structure for cutting, boring into or degrading a body, at least a part of the PCD structure comprising a volume of an embodiment of PCD material according to an aspect of the invention. In some embodiments, at least part of the volume of the PCD 30 material may have a thickness in the range from about 3.5 mm to about 12.5 mm or in the range from about 4 mm to about 7 mm. In one embodiment of the invention, the PCD structure may have a region adjacent a surface comprising at most about 2 volume percent of catalyst WO 2010/140108 PCT/IB2010/052418 8 material for diamond, and a region remote from the surface comprising greater than abUouLt 2 volume percent ofl catalyst material for diamond. I some embodiments, the region adjacent the surface may extend to a depth of at least about 20 microns, at east about 80 microns, at least anout 100 minronnr enven ptlt I abkuf An0 ro-rrns frnm thn surfae . In nne embodiment, at least a portion of the region adjacent the surface may be in the general form of a layer or stratum. An embodiment of the invention provides a tool or tool component for cutting, 10 boring into or degrading a body, comprising an embodiment of a PCD structure according to an aspect of the invention. In some embodiments, the tool or tool component may be for cutting, milling, grinding, drilling, earth boring, rock drilling or other abrasive applications, such as the cutting and machining of metal. In one embodiment, the tool component may be an insert 15 for a drill bit, such as a rotary shear-cutting bit, for boring into the earth, for use in the oil and gas drilling industry. In one embodiment, the tool may be a rotary drill bit for boring into the earth. In one embodiment, an insert comprises an embodiment of PCD material 20 according to the invention, the material bonded to a cemented carbide substrate and the insert being for a drill bit for boring into the earth. In one embodiment of the invention, the tool component may comprise an embodiment of a PCD structure bonded to a cemented carbide substrate at 25 an interface. In one embodiment, the PCD structure may be integrally formed with the cemented carbide substrate. In one embodiment, the interface may be substantially planar. In one embodiment, the interface may be substantially non-planar. 30 Drawings Non-limiting embodiments will now be described with reference to the drawings of which: WO 2010/140108 PCT/IB2010/052418 9 FIG 1 shows a schematic drawing of the microstructure of an embodiment of POD material. FiG 2 shows a processed image of a microQraphl. of a polished section of an 5 embodiment of POD material FIG 3 shows the frequency distribution of diamond grain contiguity of an embodiment of PCD material, with a fitted normal curve superimposed on the distribution. 10 FIG 4 shows a number frequency graph of equivalent circle diameter (ECD) grain size, shown on the horizontal axis, for an embodiment of PCD material. FIG 5 shows a schematic drawing of an embodiment of an insert a rotary drill 15 bit for boring into the earth. The same reference numbers refer to the same features in all drawings. Detailed description of embodiments 20 As used herein, polycrystallinee diamond" (PCD) material comprises a mass of diamond grains, a substantial portion of which are directly inter-bonded with each other and in which the content of diamond is at least about 80 volume percent of the material. In one embodiment of PCD material, interstices 25 between the diamond gains may be at least partly filled with a binder material comprising a catalyst for diamond. As used herein, "interstices" or "interstitial regions" are regions between the diamond grains of PCD material. In embodiments of PCD material, interstices or interstitial regions may be substantially or partially filled with a material other than diamond, or they may 30 be substantially empty. Embodiments of PCD material may comprise at least a region from which catalyst material has been removed from the interstices, leaving interstitial voids between the diamond grains WO 2010/140108 PCT/IB2010/052418 10 In the field of quantitative stereography, particularly as applied to cemented carbide material, "contiguity" is undestOod to ble a quantitative measure of inter-phase contact. It Is defined as the internal surface area of a phase snared w!tn grains of the same phase in a substantial twh a (I ~ ~ ~ ~ ~ nf IncrwojdEC flmnf~fna___ 5 micrnstrucre (Unerwod E.E "Qaniatv Stereorapnhy", Addison Wesley, Reading MA 1970; German, R.M. "The Contiguity of Liquid Phase Sintered Microstructures", Metallurgical Transactions A, Vol. 16A, July 1985, pp. 1247-1252). As used herein, "diamond grain contiguity" is a measure of diamond-to-diamond contact or bonding, or a combination of contact and 10 bonding within PCD material. As used herein, a "metallic" material is understood to comprise a metal in unalloyed or alloyed form and which has characteristic properties of a metal, such as high electrical conductivity. 15 As used herein, "catalyst material" for diamond, which may also be referred to as solvent / catalyst material for diamond, means a material that is capable of promoting the growth of diamond or the direct diamond-to-diamond inter growth between diamond grains at a pressure and temperature condition at 20 which diamond is thermodynamically stable. A filler material is understood to mean a material that wholly or partially fills pores, interstices or interstitial regions within a polycrystalline structure. 25 The size of grains may be expressed in terms of equivalent circle diameter (ECD). As used herein, the "equivalent circle diameter" (ECD) of a particle is the diameter of a circle having the same area as a cross section through the particle. The ECD size distribution and mean size of a plurality of particles may be measured for individual, unbonded particles or for particles bonded 30 together within a body, by means of image analysis of a cross-section through or a surface of the body. As used herein, the words "average" and "mean" have the same meaning and are interchangeable.
WO 2010/140108 PCT/IB2010/052418 11 With reference to FIG 1 and FIG 2, an embodirnient of PCD material 10 comprises diamond grains 12 having a mean diamond grain contiguity of greater man 60.5 percent. The diamond grains 12 form a skeletal mass 5 defining 6 ine ice orE; inerti.a rein 1 MI -P--: 4 bu'een them. h om ie lengths of lines passing through all points lying on all bond or contact interfaces 16 between diamond grains within a section of the PCD material are summed to determine the diamond perimeter, and the combined lengths of lines passing through all points lying on all interfaces 18 between diamond 10 and interstitial regions within a section of the PCD material are summed to determine the binder perimeter. As used herein, "diamond grain contiguity" K is calculated according to the following formula using data obtained from image analysis of a polished 15 section of PCD material: C = 100 * [2*(6 -P)]/[(2*(8 - P))+6], where 8 is the diamond perimeter, and p is the binder perimeter. 20 As used herein, the diamond perimeter is the fraction of diamond grain surface that is in contact with other diamond grains. It is measured for a given volume as the total diamond-to-diamond contact area divided by the total diamond grain surface area. The binder perimeter is the fraction of diamond grain surface that is not in contact with other diamond grains. In practice, 25 measurement of contiguity is carried out by means of image analysis of a polished section surface. The combined lengths of lines passing through all points lying on all diamond-to-diamond interfaces within the analysed section are summed to determine the diamond perimeter, and analogously for the binder perimeter. 30 Images used for the image analysis should be obtained by means of scanning electron micrographs (SEM) taken using a backscattered electron signal. Optical micrographs may not have sufficient depth of focus and may give WO 2010/140108 PCT/IB2010/052418 12 substantially different contrast. The method of measuring diamond grain contiguity requires that distinct Udiamond grains in contact with or bonded iu each other can be distinguished from single diamond grains. Adequate contrast between the diamond grains and the boundary regoo ns between them 5 may be imnnrtant fnr the measurement of configuity sine bun!rdar;es between grains may be identified on the basis of grey scale contrast. Boundary regions between diamond grains may contain included material, such as catalyst material, which may assist in identifying the boundaries between grains. 10 FIG 2 shows an example of a processed SEM image of a polished section of a PCD material 10, showing the boundaries 16 between diamond grains 12. These boundary lines 16 were provided by the image analysis software and were used to measure the diamond perimeter and subsequently for 15 calculating the diamond grain contiguity. The non-diamond regions 14 are indicated as dark areas and the binder perimeter was obtained from the cumulative length of the boundaries 18 between the diamond 12 and the non diamond or interstitial regions 14. 20 With reference to FIG 3, the measured mean diamond grain contiguity of the embodiment of PCD material, the processed image of which is shown in FIG 2, is about 62 percent. The measured data are shown fitted with a normal or Gaussian curve, from which the standard deviation of the diamond grain contiguity may be determined. 25 As used herein, the "interstitial mean free path" within a polycrystalline material comprising an internal structure including interstices or interstitial regions, such as PCD, is understood to mean the average distance across each interstitial between different points at the interstitial periphery. The 30 average mean free path is determined by averaging the lengths of many lines drawn on a micrograph of a polished sample cross section. The mean free path standard deviation is the standard deviation of these values. The diamond mean free path is defined and measured analogously.
WO 2010/140108 PCT/IB2010/052418 13 The homogeneity or uniformity of a PCD structure may be quantified by conducting a statistical evaluation using a large number of micrographs of polished sections. The distribution of the filler phase, which is easily distinguishable from that of the diamond pnase using electron microscopv. 5 can then be measured in method similar to that disclosed in EP 0 7 56 (see also W02007/110770). This method allows a statistical evaluation of the average thicknesses of the binder phase along several arbitrarily drawn lines through the microstructure. This binder thickness measurement is also referred to as the "mean free path" by those skilled in the art. For two 10 materials of similar overall composition or binder content and average diamond grain size, the material that has the smaller average thickness will tend to be more homogenous, as this implies a finer scale distribution of the binder in the diamond phase. In addition, the smaller the standard deviation of this measurement, the more homogenous is the structure. A large standard 15 deviation implies that the binder thickness varies widely over the microstructure, i.e. that the structure is not even, but contains widely dissimilar structure types. With reference to FIG 4, which shows one non-limiting example of a multi 20 modal grain size distribution for the purpose of illustration, a multimodal size distribution of a mass of grains is understood to mean that the grains have a size distribution with more than one peak 20, each peak 20 corresponding to a respective "mode". Multimodal polycrystalline bodies are typically made by providing more than one source of a plurality of grains, each source 25 comprising grains having a substantially different average size, and blending together the grains or grains from the sources. Measurement of the size distribution of the blended grains may reveal distinct peaks corresponding to distinct modes. When the grains are sintered together to form the polycrystalline body, their size distribution is further altered as the grains are 30 compacted against one another and fractured, resulting in the overall decrease in the sizes of the grains. Nevertheless, the multimodality of the grains may still be clearly evident from image analysis of the sintered article.
WO 2010/140108 PCT/IB2010/052418 14 Unless otherwise stated herein, dimensions of size, distance, perimeter, ECD, mean free path and so forth relating to grains and interstices within POD material, as well as the grain contiguity, refer to The dimensions as measured on a surface of, or a section fnrough a body comprising PCD materia and no 5 stereographic correction has hen nnipr!i For example, the size distributins of the diamond grains as shown in FIG 4 were measured by means of image analysis carried out on a polished surface, and a Saltykov correction was not applied. 10 In measuring the mean value and deviation of a quantity such as grain contiguity, or other statistical parameter measured by means of image analysis, several images of different parts of a surface or section are used to enhance the reliability and accuracy of the statistics. The number of images used to measure a given quantity or parameter may be at least about 9 or 15 even up to about 36. The number of images used may be about 16. The resolution of the images needs to be sufficiently high for the inter-grain and inter-phase boundaries to be clearly made out. In the statistical analysis, typically 16 images are taken of different areas on a surface of a body comprising the PCD material, and statistical analyses are carried out on each 20 image as well as across the images. Each image should contain at least about 30 diamond grains, although more grains may permit more reliable and accurate statistical image analysis. Catalyst material may be introduced to an aggregated mass of diamond 25 grains for sintering in any of the ways known in the art. One way includes depositing metal oxide onto the surfaces of a plurality of diamond grains by means of precipitation from an aqueous solution prior to forming their consolidation into an aggregated mass. Such methods are disclosed in PCT publications numbers W02006/032984 and also W02007/110770. Another 30 way includes preparing or providing metal alloy including a catalyst material for diamond, such as cobalt-tin alloy, in powder form and blending the powder with the plurality of diamond grains prior to their consolidation into an aggregated mass. The blending may be carried out by means of a ball mill. Other additives may be blended into the aggregated mass.
WO 2010/140108 PCT/IB2010/052418 15 in one embodiment, Lie aggregated mass of diamond grains, including any catalyst material particles or additive material particles that may have been introduced, may be formed into an unbonded or loosev bonded Structure, 5 whirh may be placed onto a cemented carbide substrate. The cemented carbide substrate may contain a source of catalyst material for diamond, such as cobalt. The assembly of aggregated mass and substrate may be encapsulated in a capsule suitable for an ultra-high pressure furnace apparatus capable of subjecting the capsule to greater than 6GPa. Various 10 kinds of ultra-high pressure apparatus are known and can be used, including belt, torroidal, cubic and tetragonal multi-anvil systems. The temperature of the capsule should be high enough for the source of catalyst material to melt and low enough to avoid substantial conversion of diamond to graphite. The time should be long enough for sintering to be completed but as short as 15 possible to maximise productivity and reduce costs. PCT publication number W02009/027948 describes polycrystalline diamond material comprising a diamond phase and a filler material, the filler material comprising ternary carbide, and PCT publication number W02009/027949 20 describes polycrystalline diamond material comprising inter-grown diamond grains and a filler material comprising a tin-based inter-metallic or ternary carbide compound formed with a metallic catalyst. PCD material according to the invention has the advantage of enhanced 25 abrasion resistance. It may also have the advantage of enhanced strength and enhanced thermal stability. Any or all of these advantages may result from the enhanced diamond contiguity of the PCD material. If the mean diamond grain contiguity is substantially less than about 60 percent, enhanced abrasion resistance, strength or thermal stability, or a combination of these 30 properties, may not be exhibited. In some embodiments of the invention, enhanced diamond grain contiguity may arise from the use of diamond grains having a multimodal size distribution in which the grain size distribution characteristics are selected according to an embodiment of the invention. If the standard deviation of the diamond grain contiguity is substantially greater WO 2010/140108 PCT/IB2010/052418 16 than about 4 percent contiguity, then the advantages arising from having high * k ,~al grain4 mean grain contiguity may De sUuLantially reduced. If the diamond grain contiguity is substantially greater than about 80 percent or even greater than anut 77 percent, then the fracture resistance oT ren PCD material may fle Tflfl 5 low. If the volume of the PD material is substanfially ls than about 0 5 mm 2 , then it may be too small for practical use in certain cutting or drilling operations. Embodiments of the invention have enhanced strength, abrasion resistance 10 and thermal stability. Enhanced contiguity and inter-grain bonding may result in increased strength, abrasion resistance and thermal stability. While wishing not to be bound by theory, increased thermal stability or resistance may be due to reduced interfacial area between catalyst material and diamond within the microstructure. 15 Embodiments of PCD material according to the invention exhibit enhanced diamond contiguity and enhanced inter-grain bonding, more homogeneous spatial distribution of the diamond grains, less porosity and lower overall catalyst content, all of which may generally be regarded as beneficial. 20 Improved homogeneity may result in less variability in the performance of the PCD in use. In some embodiments of the invention, the combination of high contiguity and / or high homogeneity and I or reduced content of metallic catalyst within the 25 PCD on the one hand, and a size distribution comprising at least two peaks or modes, or at least three peaks or modes, on the other may result in substantial improvement in wear resistance and other properties of the PCD, and consequently enhanced working life and cutting or penetration rate of the polycrystalline diamond element in rock drilling or earth boring applications, 30 and shear cutting rock drilling in particular. This combination of features may be synergistic. Metallic catalyst materials for diamond may result in excellent inter-grain diamond bonding and sintering, and consequently in PCD material having WO 2010/140108 PCT/IB2010/052418 17 high abrasion resistance and strength. However, residual metallic catalyst material may remain within the sintered PCD, located within interstices between the diamond grains, and may reduce the thermal stability of the PCD imateria. "Thermal stability" refers to the relative insensitivity nf keny i pr - matra such as sin rin an strength, as a function of temperature, particularly to temperatures up to about 700 degrees centigrade or even up to about 800 degrees centigrade. Sintering PCD material using pressures greater than 6.0 GPa may tend to enhance the thermal stability PCD comprising metallic filler material. 10 Reduced content of catalyst material in the sintered PCD may enhance thermal stability. This may be because catalyst material may promote the re conversion of diamond to graphite at the elevated temperatures and ambient pressure that typically prevail in use. Such re-conversion may significantly weaken the PCD material. In addition, metallic catalyst material generally has 15 much higher thermal coefficient of expansion than diamond and its presence may increase internal stresses within the PCD as the temperature increases or decreases, which may weaken the material. Metallic catalyst material is may also be vulnerable to oxidation, which may further increases internal stresses. 20 Embodiments of tools according to the invention have enhanced performance. In particular, earth boring drilling bits equipped with inserts comprising PCD with enhanced diamond grain contiguity and sintered using a pressure of greater than 6 GPa may exhibit superior performance in oil and gas drilling 25 applications. Similar benefits may also be derived where other catalyst materials are used. If the pressure used to sinter the PCD material is less than about 6 GPa, the diamond grain contiguity and may not be high enough, and certain 30 mechanical properties such as abrasion resistance, thermal stability and strength may not be substantially enhanced. In embodiments of the method of the invention, it may be desirable for the pressure to be as low as possible, but still greater than 6 GPa, in order to permit larger reaction volumes to be used and consequently larger articles to be sintered. Use of lower pressures WO 2010/140108 PCT/IB2010/052418 18 may reduce costs and engineering complexity. In some embodiments of the method of the invention where the diamond grains have an average size of 1I micron or less, a sintering pressure of greater than about 7.0 GPa may result nm proved sine sub-micron damnd rains Embodiments of the method of the invention have the advantage that higher temperatures can be used to form the PCD material by sintering, which may be beneficial for the properties of the material; especially where the filler material and / or catalyst material used has a relatively high melting point. 10 Embodiments of the method of the invention may be particularly beneficial where the polycrystalline diamond material includes a filler material comprising ternary carbide material, and the thermal stability of the PCD material in particular may be enhanced. This may arise because ternary 15 metal carbide may be relatively inert with respect to diamond. Embodiments of the method of the invention may be particularly beneficial for a type of PCD material that includes a filler material comprising a tin-based inter-metallic or ternary carbide compound formed with a metallic catalyst for diamond. Embodiments of the method of the invention may be particularly beneficial for 20 making PCD material having a filler material comprising cobalt and tin, particularly in which the average diamond grain size is less than about 10 micron, and in which at least some of the filler material is introduced by infiltration. Embodiments of the method of the invention have the advantage of substantially reducing the incidence of defects associated with poor 25 sintering, which tend to occur near the upper surface of a PCD structure. Consequently fewer PCD elements may be rejected, resulting in improved process economics. The PCD material may tend to have enhanced strength, abrasion resistance and thermal stability, including oxidation resistance. 30 The thermal stability of embodiments of PCD material according to the invention, particularly the oxidation onset temperature as measured by means of thermo-gravimetric analysis (TGA), may be substantially enhanced. Embodiments such as these may be thermally stable and exhibit superior performance in applications such as oil and gas drilling, wherein the WO 2010/140108 PCT/IB2010/052418 19 temperature of a PCD cutter element can reach above about 700 degrees centigrade. Oxidation onset temperature is measured by means of thermo gravimetric analysis (TGA) in the presence of oxygen, as is known in the art. advantageous for the cutting or machining of metal, owing to the enhanced thermal stability and resistance of the PCD material. Examples 10 Embodiments of the invention are described in more detail with reference to the examples below, which are not intended to limit the invention. Example 1 15 An aggregated mass of diamond grains having a mean size of about 8 microns was formed by blending diamond powder from two sources having respective mean grain sizes in the range from about 1 micron to about 4 microns and in the range from about 7 microns to about 15 microns. The 20 blended diamond grains were treated in acid to remove surface impurities that may have been present. Vanadium carbide (VC) powder and cobalt (Co) powder were introduced into the diamond powder by blending particles of VC and Co with the diamond powder using a planetary ball mill. The mean size of the VC particles was about 4 microns and the content of the VC in the 25 aggregated mass was about 3 weight percent. The aggregated mass was then formed into a layer on a substrate comprising Co-cemented tungsten carbide (WC) and encapsulated within a capsule for an ultra-high pressure furnace to form a pre-sinter assembly, which was then out-gassed in a vacuum to remove surface impurities from the diamond grains, as is known in 30 the art. The diameter of the substrate was a little greater than about 13mm and the height was about 10mm. The pre-sinter assembly was subjected to a pressure of about 6.8 GPa and a temperature of about 1,600 degrees centigrade in an ultra-high pressure WO 2010/140108 PCT/IB2010/052418 20 furnace to sinter the diamond grains and form a PCD compact comprising a layer of PCD material integrally formed with the carbide substrate. The POD layer was about 2mm thick. During the sintering process, molten cobalt from the substrate and containing disiCedinr I nr WC 5rbthi n iitrated d. or both in souo n -rae A section was cut from the PCD material and a section surface was polished. Sixteen digital images of microscopic areas were obtained at different respective positions on the section surface by means of scanning electron 10 micrography (SEM) using a backscattered electron signal. The resolution of the images was 0.04717 micrometers per pixel. Each of the images was subjected to image analysis to measure the mean diamond grain contiguity, the mean diamond grain ECD, the mean interstitial ECD, the diamond grain mean free path and the interstitial mean free path, as well as the standard 15 deviations of each of these quantities. These quantities were then averaged over those obtained for all the images. In the case of the diamond grain and interstitial ECD size measurement, the size distribution was characterised more fully, as described below. In performing the image analysis, the contrast between the diamond grains and the boundary regions between diamond 20 grains was adjusted to emphasise boundaries between grains on the basis of grey scale contrast. The image analysis was performed using software having the trade name analySIS Pro from Soft Imaging System@ GmbH (a trademark of Olympus 25 Soft Imaging Solutions GmbH) may be used. This software has a "Separate Grains" filter, which according to the operating manual provides satisfactory results if the structures to be separated are closed structures. Therefore, it is important to fill up any holes before applying this filter. The "Morph. Close" command, for example, may be used or help may be obtained from the 30 "Fillhole" module. In addition to this filter, the "Separator" is another powerful filter available for grain separation. This separator can also be applied to color- and gray-value images, according to the operating manual.
WO 2010/140108 PCT/IB2010/052418 21 Results of the image analysis are summarised in Tables 1 and 2. The content of diamond was measured to be about 90.8 volume percent, the diamond grain contiguity was about 68.4 percent and the mean size of the sintered diamond grains was bout 63 microns terms of eculvalent circrIe diameter. r The aveage intersitia m-n fre path othP mri was about fl=52 (±0.46) micron. The data relate to two dimensional measurements taken from image analysis of a scanning electron micrograph, and has not been corrected for three 10 dimensions. For example, the quoted mean diamond grain size is the mean size corresponding to the cross-sectional areas of diamond grains. The diamond and interstitial sizes are calculated as equivalent circle diameters (ECD), by determining the cross-sectional area and calculating the diameter of a circle having the area. The statistical parameters d10, d50, d75 and d90 15 refer to the sizes (ECD) for which 10 percent, 50 percent, 75 percent and 90 percent, respectively, of grains are less than. The maximum size is the size for which substantially no grains are greater. The parameters "Lower (95 percent)" and "Upper (95 percent)" refer to the size values for which 5 percent of grains are less than and greater than, respectively. 20 Mean, Standard d1O, d5O, d75, d9O, Maximum, deviation, microns d con microns microns microns microns micron Diamonds grand 6.30 2.52 2.77 6.17 8,06 9.10 12.40 Intestitial 1.75 0.90 0.63 1.63 2.26 2.94 3.98 ranMFP 4.51 4.96 0.33 2.74 6.65 11.04 49.25 IntersPtial 0.52 0.46 0.09 0.38 0.71 1.13 4.72 *MFP is mean free path Table 1 WO 2010/140108 PCT/IB2010/052418 22 (95 cemcent) (95 Dercent) inT tZ ~ a Mean, percent Standard deviation 95o- r nt29 e t Diamon rcnent, interstitial, percent area 9.25 0..56 8.95 9.55 Diamond contiguity, 68.0 1.15 67.4 68.6 percent Table 2 5 Example 2 An aggregated mass of diamond grains having a mean size of about 10 microns was formed by blending diamond powder from five sources having respective mean grain size in the range from about 0.5 micron to about 3 10 microns, in the range from about 2 microns to about 5 microns, in the range from about 4 microns to about 9 microns, in the range from about 7 microns to about 15 microns and in the range from about 10 microns to about 30 microns. The blended diamond grains were treated in acid to remove surface impurities that may have been present. Vanadium carbide (VC) powder and 15 cobalt (Co) powder were introduced into the diamond powder by blending particles of VC and Co with the diamond powder using a planetary ball mill. The mean size of the VC particles was about 4 microns and the content of the VC in the aggregated mass was about 3 weight percent. The aggregated mass was then formed into a layer on a substrate comprising Co-cemented 20 tungsten carbide (WC) and encapsulated within a capsule for ultra-high pressure furnace to form a pre-sinter assembly, which was then out-gassed in a vacuum to remove surface impurities from the diamond grains, as is known in the art. The diameter of the substrate was a little greater than about 13mm and the height was about 2mm. 25 The pre-sinter assembly was subjected to a pressure of about 8GPa and a temperature of about 1,700 degrees centigrade in an ultra-high pressure furnace to sinter the diamond grains and form a PCD compact comprising a WO 2010/140108 PCT/IB2010/052418 23 layer of PCD material integrally formed with the carbide substrate. The PCD layer was about 2mm thick. During the sintering process, molten cobalt from the substrate and containing dissolved W or WC, or both, in solution infiltrated into the aggregate mass of diamond crains SEM images of the PCD material were obtained as described in Example 1, except that the resolution of the images was 0.09434 micrometers per pixel. Results of image analysis of the images are shown in Table 3 and Table 4 below. The content of diamond was about 90.7 volume percent, the diamond 10 grain contiguity was about 70.3 percent and the mean size of the sintered diamond grains was about 7.4 microns in terms of equivalent circle diameter. Mean, Standard d10, d50, d75, d90, Maximum, microns dmicon microns. microns microns microns micron Diamond 7.4 3.4 2.8 6.9 9.9 12.0 142 grain size Intes tial 2.95 1.41 1.0 2.9 3.9 4.8 5 gaMoP 5.0 6.1 0.23 2.7 7.2 13.0 58.9 IntFtial 0.66 0.68 0.09 0.42 0.89 1.5 7.04 *MFP is mean free path 15 Table 3 Mean, percent Standard deviation Lower (95 percent) Upper (95 percent) Diamond content, 90.7 0.56 90.4 91.0 percent area Interstitial, percent area 9.2 0.56 8.9 9.55 Diamond contiguity, 70,3 1.9 69.2 71.3 percent Table 4 WO 2010/140108 PCT/IB2010/052418 24 The PCD compact was processed to form a test PCD cutter insert, which was subjected to a wear test. The wear test involved using the insert in a vertical turret milling apparatus to cut a length of a workpiece material comprising i -1 h---------- --. r1 h-, e.- cc P-vf-A indication of expected working life in use. The cutting distance achieved with the test insert was about 75 percent greater than that achieved using a control PCD cutter insert, which had been sintered at a pressure of about 5.5GPa and which contained no VC additive. The abrasion resistance of the test cutter 10 insert was observed to be substantially enhanced. Example 3 Test and control PCD material samples were prepared using sintering 15 pressures of 6.8 GPa and 5.5 GPa, respectively. In all other respects the test and control samples were made in the same way. Raw material diamond powder was prepared by blending diamond grains from three sources, each source having a different average grain size distribution. The size distribution of the grains within the resulting blended powder had the size distribution 20 characteristic that 9.8 weight percent of the grains had average grain size less than 5 microns, 7.6 weight percent of the grains had average size in the range from 5 microns to 10 microns, and 82.6 weight percent of the grains had average grain size greater than 10 microns. The blended diamond grains had an average size of approximately 20 micron. 25 Cobalt and tin were deposited onto the surfaces of the diamond grains by means of a method including depositing cobalt and tin oxides onto the surfaces from an aqueous solution. The cobalt-tin accounted for about 7.5 percent of the coated diamond mass, and was found to be dispersed over the 30 grain surfaces as nano-scale formations. The cobalt-tin coated diamond grains were formed into an aggregated mass on a surface of a cobalt-cemented tungsten carbide substrate, and this assembly was encapsulated within a refractory metal jacket to form a pre- WO 2010/140108 PCT/IB2010/052418 25 compact assembly, from which air was subsequently removed. The pre compact assembly was loaded into a capsule for a high-pressure high temperature furnace. * _k iit.~i; .c VJ~ll% V,-~ _d Z a C- -4 temperature of 1,550 degrees centigrade for about 9 minutes to form a compact comprising a sintered PCD mass bonded to a tungsten carbide substrate. 10 The control material was subjected to a conventionally used pressure of about 5.5 GPa and a temperature of about 1,450 degrees centigrade for about 9 minutes to form a compact comprising a sintered PCD mass bonded to a tungsten carbide substrate. 15 The compacts were substantially cylindrical in shape, having a diameter of about 16 mm. The compacts comprised a layer of PCD integrally bonded onto a cobalt-cemented tungsten carbide (WC) substrate, the PCD layers being 2.2 mm thick. The diamond content of the PCD layer was about 92 percent by volume, the balance being cobalt and minor precipitated phases 20 such as WC. The diamond grains within the PCD thus produced had a multimodal size distribution having the characteristic that 34.7 weight percent of the grains had average grain size less than 5 microns, 40.4 weight percent of the grains had average size in the range from 5 microns to 10 microns, and 24.9 weight percent of the grains had average grain size greater than 10 25 microns. The grain size distribution of the sintered PCD is different from that of the input grains due to mutual crushing of the grains at high pressure, in addition to the shift towards coarser grain sizes that normally occurs during the sintering process. 30 The control and test compacts were analysed. Both were found to comprise PCD with the following phases present in the interstices: Co 3 Sn 2 , Co 3 SnCo, CoSn, Co and WC. The major phase was Co 3 SnCO 7 , and it is believed that this phase plays a major role in improving the thermal stability of the PCD. The other phases were present in trace quantities.
WO 2010/140108 PCT/IB2010/052418 26 image analysis was used to analyse the inter-growth of the diamond grains as well as the homogeneity of their spatial distribution within the PCD. A higher degree of diamond grain nter-grnwth was observed ni1thin the PCD of the test !7 - --- -- -- -- f~ -r - intergrowth and contact can be expressed in terms of diamond grain contiguity, the average contiguity of the test PCD being 62.0 percent (±1.9 percent), compared to the control PCD average contiguity of being 59.2 percent (± 1.4 percent), the figure in brackets being the standard deviation). 10 Statistically, this absolute difference of 2.8 percent may be substantial, since an absolute difference in contiguity of 0.8 percent corresponds to a confidence interval of 95 percent. The average interstitial mean free path of the test PCD was about 0.74 15 (±0.62) micron, compared to the control PCD average of 1.50 (±2.53) micrometers. More cobalt was present in the test PCD than in the control PCD, the additional cobalt having infiltrated from the cobalt-containing substrate, it is 20 believed. This resulted in the test PCD having a higher content of Co 3 SnCo than the control PCD. Additionally, the content of WC was higher in the test PCD, which contained a greater quantity of re-crystallised WC "plume" formations near the interface with the substrate. 25 Results of image analysis of the test material are summarised in Tables 5 and 6. The data relate to two dimensional measurements taken from image analysis of a scanning electron micrograph, and has not been corrected for three dimensions. The parameters in the table have the same meaning as described in Example 1.
WO 2010/140108 PCT/IB2010/052418 27 Mean, Stadard d10, d5, d7d, J Maximum, microns microns m t t grain size 114 4.J I 5 A Io0 Ii19.23 Interstitial 2.19 1.08 0.80 2.01 3.42 3.5 5.48 size Diamond grn MFP* 5.94 7.09 0.38 3.11 8.3 15.47 67.92 Mn 0.68 0.60 0.19 0.47 0.94 1.42 6.51 *MFP is mean free path Table 5 5 Mean, percent Standard deviation Lower (95 percent) Upper (95 percent) Diamond content, 90.54 0.57 90.24 90.84 percent area Interstitial, percent area 9.46 0.57 9.16 9.76 Diamond contiguity, 62.05 1.86 61.06 63-04 percent Table 6 Both the control and test samples were processed to form inserts suitable for 10 rock boring, and subjecting the inserts to a wear test that involved using the inserts to machine a granite block mounted on a vertical turret milling apparatus. This test involved machining a granite block over a number of passes and measuring the size of the wear scar formed into the PCD as a result of abrasive wear against the granite. After 50 passes, wear scar of the 15 test PCD was about 30 percent smaller than that of the control PCD, and lasted at least another 100 passes in working condition. When several more samples of test and control PCD were manufactured, it was found that the quality of the test PCD was much more consistent than 20 that of the control PCD, and the reject rate was much lower.
WO 2010/140108 PCT/IB2010/052418 28 it has been found that the use of a method according to the first aspect of the invention permits thick PCD structures to be sintered. Thicker POD structures have greater strength. all else being enuai, than thinner P-D structures. Example 4 Several samples of Co-Sn-based PCD sintered onto a cemented carbide substrate were prepared. In each case, tin powder was pre-reacted with 10 cobalt metal powder to produce a CoSn alloy ! intermetallic of specific atomic ratio 1:1. This pre-reacted source was then introduced into an unsintered diamond powder mass by either pre-synthesis admixing or in situ infiltration. The 1:1 CoSn pre-reacted powder mixture was prepared by milling the Co and Sn powders together in a planetary ball mill. The powder mixture was then 15 heat- treated in a vacuum furnace (600 degrees centigrade to 800 degrees centigrade) to manufacture reacted CoSn material. This pre-reacted material was then further crushed I milled to break down agglomerates and reduce the grain size. The diamond powder size distribution had an average grain size of less than about 10 microns. A chosen amount of this CoSn material 20 (expressed as a weight percent of the diamond powder mass) was then brought into contact with the unsintered diamond powder within an ultra-high pressure furnace reaction volume. This was either as a discrete powder layer adjacent to the diamond powder mass (which would infiltrate the diamond during ultra-high pressure treatment after melting, i.e. in situ infiltration) or the 25 CoSn material was admixed directly into the diamond powder mixture before the canister was loaded. The diamond powder / CoSn assembly was then placed adjacent a cemented carbide substrate such that the binder metallurgy was then further augmented by the infiltration of additional cobalt from the cemented carbide substrate at the ultra-high pressure conditions. The 30 assembly was subjected to a pressure of about 6.8 GPa and a temperature above the melting point of cobalt. In this way, a range of Co : Sn ratio binder systems and resultant PCD materials was produced.
WO 2010/140108 PCT/IB2010/052418 29 Example 5 A mono-modai PCiD test material was prepared by blending cobalt powder witth damond grains by means of a planetary ball mill. and sintering the degrees centigrade for a period of about 60 seconds. The diamond grains had average size in the range from 3 micron to 6 micron. The weight ratio of cobalt to diamond in the blended powder mix was 18 : 82. Free-standing, unsupported sintered PCD samples having diameter of 13.7 mm and height of 10 4 mm were produced. A control PCD material was made similarly to the test material, except that i) the cobalt was introduced by infiltration from a cemented tungsten carbide substrate, as is conventional, resulting in a weight ratio of cobalt to diamond 15 was 26 : 74, and ii) a sintering pressure of 5.5 GPa and temperature of about 1,450 degrees centigrade was used. A scanning electron micrograph of a polished section of the sintered test PCD was obtained using backscattered electrons, and image analysis was carried 20 out on the micrograph. Results of image analysis of the test material are summarised in Tables 7 and 8, the parameters having the same meaning as defined in Example 1.
WO 2010/140108 PCT/IB2010/052418 30 Mean, Standard d10, d50, d75, d90, Maximum, microns o icrWoaS mcns icron s mkoz mK>cronS micron rDiamond 1 C .
1 1
.
1
.
1 t grain size 4.3 1.7 7.12 7.33 9.09 interstital 1.11 0.58 0.41 0.98 1.49 1.68 3.14 sizeI gaMFP 3.63 3.30 0.47 2.74 4.74 8.23 46.18 IntMtial 0.32 0.31 0.05 0.23 0.47 0.74 340 *MFP is mean free path Table 7 5 Mean, percent Standard deviation Lower (95 percent) Upper (95 percent) Diamond content, 9124 0.35 91.05 91.43 percent area Interstitial, percent area 8.76 0.35 8.57 8.95 Diamond contiguity, 73.54 0.67 73.19 73.90 percent Table 8 The test and control samples were formed into cutting inserts by conventional 10 processing and subjected to a wear test involving the milling of granite. A depth of cut of 1 mm depth was used. The output of the wear test is a cutting length, which is the distance of granite milled before the cutter is deemed to have failed. The cutting length of the test PCD was about 5,100 mm, which is significantly greater than the control PCD cutting length of about 1,200 mm. 15 This indicates that the abrasive wear resistance of the test PCD is several times greater than that of the control PCD.

Claims (20)

1. A poiycrystaiiine diamond (POD) material comprising at least 86 volume percent and at mo s t 90 volume percent diamond rains. the mean
2. A PCD material as claimed in claim 1, the diamond grain contiguity being at most 80 percent. 10
3. A PCD material as claimed in claim 1 or claim 2, the standard deviation of the diamond grain contiguity being at most 4 percent contiguity.
4. A PCD material as claimed in any one of the preceding claims, the 2 material having a volume of at least 0.5 mm 15
5. A PCD material as claimed in any one of the preceding claims, the diamond grains having the size distribution characteristic that at least 50 percent of the grains have average size greater than 5 microns. 20
6. A PCD material as claimed in any one of the preceding claims, comprising diamond grains having a multimodal size distribution.
7. A PCD material as claimed in any one of the preceding claims, comprising diamond grains having a mean size of at most 15 microns. 25
8. A PCD material as claimed in any one of the preceding claims, having an average interstitial mean free path of at most 1.5 microns.
9. A PCD material as claimed in any one of the preceding claims, in which 30 the standard deviation of the interstitial mean free path is in the range from 0.05 microns to 1.5 micron.
10.A PCD material as claimed in any one of the preceding claims, having a mean interstitial ECD size of at least 0.5 micron and at most 4 microns.
WO 2010/140108 PCT/IB2010/052418 32 I1.A PCD material as claimed in any one of the preceding claims, including a fifler material comprising a ternary carbide of the iormuia Mx M'y Cz, M beino at least one element selected from the group consisting ot the 5 transition metalsc andI_ the rare consmeai;sMtbing ane e t eete from the group consisting of Al, Ga, In, Ge, Sn, Pb, TI, Mg, Zn and Cd; x being in the range from 2.5 to 5.0; y being in the range from 0.5 to 3.0; and z being in the range from 0.1 to 1.2. 10
12.A PCD material as claimed in claim 11, in which M is selected from the group consisting of Co, Fe, Ni, Mn, Cr, Pd, Pt, V, Nb, Ta, Ti, Zr, Ce, Y, La and Sc.
13.A PCD material as claimed in any one of the preceding claims, having an 15 oxidation onset temperature of at least 800 degrees centigrade.
14.A PCD material as claimed in any one of the preceding claims, having a region adjacent a surface comprising at most 2 volume percent of catalyst material for diamond, and a region remote from the surface comprising 20 greater than 2 volume percent of catalyst material for diamond.
15.An insert comprising PCD material as claimed in any one of the preceding claims bonded to a cemented carbide substrate, the insert being for a drill bit for boring into the earth. 25
16.A method of making PCD material as claimed in any one of claims 1 to 14, the method including subjecting an aggregated mass of diamond grains to a pressure treatment at a pressure of greater than 6.0 GPa in the presence of a metallic catalyst material for diamond at a temperature 30 sufficiently high for the catalyst material to melt, and sintering the diamond grains to form PCD material; the diamond grains in the aggregated mass having the size distribution characteristic that at least 50 percent of the grains have an average size of greater than 5 microns, and at least 20 WO 2010/140108 PCT/IB2010/052418 33 percent of the grains have an average size in the range from 10 to 15 microns.
1 7.A Meho as daim.in^"m1. inc1-Ii~nqsbetn h C aeilt
18.A method as claimed in claim 16 or claim 17, including removing metallic catalyst material for diamond from interstices between the diamond grains of the PCD material. 10
19.A method as claimed in any one of claims 16 to claim 18, including subjecting the PCD material to a heat treatment at a temperature of at least 500 degrees centigrade for at least 5 minutes. 15
20.A method as claimed in any one of claims 16 to claim 19, including introducing an additive material into the aggregated mass, the additive material containing at least one element selected from V, Ti, Mo, Zr, W, Ta, Hf, Si, Sn or Al.
AU2010255345A 2009-06-01 2010-05-31 Polycrystalline diamond Abandoned AU2010255345A1 (en)

Applications Claiming Priority (5)

Application Number Priority Date Filing Date Title
GB0909350A GB0909350D0 (en) 2009-06-01 2009-06-01 Ploycrystalline diamond material and method of making same
GB0909350.1 2009-06-01
US18320809P 2009-06-02 2009-06-02
US61/183,208 2009-06-02
PCT/IB2010/052418 WO2010140108A1 (en) 2009-06-01 2010-05-31 Polycrystalline diamond

Publications (1)

Publication Number Publication Date
AU2010255345A1 true AU2010255345A1 (en) 2011-12-15

Family

ID=40902364

Family Applications (1)

Application Number Title Priority Date Filing Date
AU2010255345A Abandoned AU2010255345A1 (en) 2009-06-01 2010-05-31 Polycrystalline diamond

Country Status (8)

Country Link
EP (1) EP2438030A1 (en)
JP (1) JP2012528780A (en)
KR (1) KR20120058469A (en)
CN (1) CN102712544A (en)
AU (1) AU2010255345A1 (en)
CA (1) CA2762306A1 (en)
GB (1) GB0909350D0 (en)
WO (1) WO2010140108A1 (en)

Families Citing this family (16)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB201006821D0 (en) * 2010-04-23 2010-06-09 Element Six Production Pty Ltd Polycrystalline superhard material
GB201008093D0 (en) * 2010-05-14 2010-06-30 Element Six Production Pty Ltd Polycrystalline diamond
GB201113391D0 (en) 2011-08-03 2011-09-21 Element Six Abrasives Sa Super-hard construction and method for making same
US9193038B2 (en) 2011-12-09 2015-11-24 Smith International Inc. Method for forming a cutting element and downhole tools incorporating the same
GB201122365D0 (en) 2011-12-28 2012-02-01 Element Six Abrasives Sa Method of making polycrystalline diamond material
US9482056B2 (en) 2011-12-30 2016-11-01 Smith International, Inc. Solid PCD cutter
GB201205716D0 (en) 2012-03-30 2012-05-16 Element Six Abrasives Sa Polycrystalline diamond material and method of forming
CN102678057B (en) * 2012-05-22 2015-01-21 株洲西迪硬质合金科技有限公司 Diamond composite sheet and preparation method thereof
GB201210658D0 (en) * 2012-06-15 2012-08-01 Element Six Abrasives Sa Superhard constructions & methods of making same
GB201210653D0 (en) * 2012-06-15 2012-08-01 Element Six Abrasives Sa Superhard constructions & methods of making same
GB201210678D0 (en) * 2012-06-15 2012-08-01 Element Six Abrasives Sa Polycrystalline diamond structure
GB201215565D0 (en) * 2012-08-31 2012-10-17 Element Six Abrasives Sa Polycrystalline diamond construction and method for making same
GB2515580A (en) * 2013-06-30 2014-12-31 Element Six Abrasives Sa Superhard constructions & methods of making same
US10167675B2 (en) * 2015-05-08 2019-01-01 Diamond Innovations, Inc. Polycrystalline diamond cutting elements having lead or lead alloy additions
US20170066110A1 (en) * 2015-09-08 2017-03-09 Baker Hughes Incorporated Polycrystalline diamond, methods of forming same, cutting elements, and earth-boring tools
CN109161815B (en) * 2018-09-21 2020-11-10 中北大学 High-phosphorus IF steel and smelting method thereof

Family Cites Families (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
RU2220929C2 (en) 1998-07-22 2004-01-10 Сумитомо Электрик Индастриз, Лтд. Sintered blanc from boron nitride with cubic lattice (options)
EP1452614B1 (en) * 2001-11-09 2017-12-27 Sumitomo Electric Industries, Ltd. Sintered diamond having high thermal conductivity
US20050133277A1 (en) 2003-08-28 2005-06-23 Diamicron, Inc. Superhard mill cutters and related methods
RU2355865C2 (en) * 2003-12-11 2009-05-20 Элемент Сикс (Пти) Лтд. Polycrystalline diamond abrasive element
EP1794252B1 (en) 2004-09-23 2012-08-22 Element Six (Pty) Ltd Polycrystalline abrasive materials and method of manufacture
JP5013156B2 (en) * 2005-07-21 2012-08-29 住友電気工業株式会社 High hardness diamond polycrystal and method for producing the same
US20070056778A1 (en) 2005-09-15 2007-03-15 Steven Webb Sintered polycrystalline diamond material with extremely fine microstructures
KR101410154B1 (en) 2006-03-29 2014-06-19 엘리먼트 씩스 (프로덕션) (피티와이) 리미티드 Polycrystalline abrasive compacts
CN101605918B (en) * 2007-02-05 2012-03-21 六号元素(产品)(控股)公司 Polycrystalline diamond (pcd) materials
CA2692216A1 (en) 2007-08-31 2009-03-05 Element Six (Production) (Pty) Ltd Polycrystalline diamond composites
GB0810184D0 (en) * 2008-06-04 2008-07-09 Element Six Production Pty Ltd Method for producing a compact

Also Published As

Publication number Publication date
CA2762306A1 (en) 2010-12-09
GB0909350D0 (en) 2009-07-15
WO2010140108A1 (en) 2010-12-09
CN102712544A (en) 2012-10-03
EP2438030A1 (en) 2012-04-11
KR20120058469A (en) 2012-06-07
JP2012528780A (en) 2012-11-15

Similar Documents

Publication Publication Date Title
US8490721B2 (en) Polycrystalline diamond
AU2010255345A1 (en) Polycrystalline diamond
EP2132348B1 (en) Abrasive compacts
GB2528732A (en) Superhard Constructions & Methods of making same
US10221629B2 (en) Polycrystalline super hard construction and a method for making same
US20150298292A1 (en) A polycrystalline super hard construction and a method for making same
US20150284827A1 (en) Polycrystalline super hard construction and a method for making same
US20180029130A1 (en) Polycrystalline diamond construction and method for making same
US20190184524A1 (en) Polycrystalline diamond construction & method of making
US20190330118A1 (en) Super hard constructions & methods of making same
WO2015140230A1 (en) Superhard pcd constructions and methods of making same
GB2515580A (en) Superhard constructions & methods of making same
US20150259987A1 (en) Polycrystalline super hard construction and a method for making same
EP4021868B1 (en) Polycrystalline diamond with iron-containing binder
US20200361000A1 (en) A polycrystalline super hard construction and a method of making same

Legal Events

Date Code Title Description
PC1 Assignment before grant (sect. 113)

Owner name: ELEMENT SIX ABRASIVES S.A.

Free format text: FORMER APPLICANT(S): ELEMENT SIX (PRODUCTION) (PTY) LTD

MK1 Application lapsed section 142(2)(a) - no request for examination in relevant period