WO2018074275A1 - 複合焼結体 - Google Patents
複合焼結体 Download PDFInfo
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- WO2018074275A1 WO2018074275A1 PCT/JP2017/036588 JP2017036588W WO2018074275A1 WO 2018074275 A1 WO2018074275 A1 WO 2018074275A1 JP 2017036588 W JP2017036588 W JP 2017036588W WO 2018074275 A1 WO2018074275 A1 WO 2018074275A1
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- 239000002131 composite material Substances 0.000 title claims abstract description 112
- 239000000463 material Substances 0.000 title abstract description 7
- 239000002245 particle Substances 0.000 claims abstract description 173
- 229910003460 diamond Inorganic materials 0.000 claims abstract description 105
- 239000010432 diamond Substances 0.000 claims abstract description 105
- 239000011230 binding agent Substances 0.000 claims abstract description 78
- 229910052582 BN Inorganic materials 0.000 claims abstract description 32
- PZNSFCLAULLKQX-UHFFFAOYSA-N Boron nitride Chemical compound N#B PZNSFCLAULLKQX-UHFFFAOYSA-N 0.000 claims abstract description 32
- 229910017052 cobalt Inorganic materials 0.000 claims abstract description 31
- 239000010941 cobalt Substances 0.000 claims abstract description 31
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 claims abstract description 31
- 239000000126 substance Substances 0.000 claims description 37
- 239000010936 titanium Substances 0.000 claims description 29
- 229910052719 titanium Inorganic materials 0.000 claims description 28
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 claims description 19
- 239000011651 chromium Substances 0.000 claims description 17
- 239000010955 niobium Substances 0.000 claims description 17
- 229910052715 tantalum Inorganic materials 0.000 claims description 17
- 229910052804 chromium Inorganic materials 0.000 claims description 16
- 229910052735 hafnium Inorganic materials 0.000 claims description 16
- 229910052750 molybdenum Inorganic materials 0.000 claims description 16
- 229910052758 niobium Inorganic materials 0.000 claims description 16
- 229910052721 tungsten Inorganic materials 0.000 claims description 16
- 229910052782 aluminium Inorganic materials 0.000 claims description 15
- 229910052710 silicon Inorganic materials 0.000 claims description 15
- 229910052726 zirconium Inorganic materials 0.000 claims description 15
- 150000004767 nitrides Chemical class 0.000 claims description 9
- GUVRBAGPIYLISA-UHFFFAOYSA-N tantalum atom Chemical compound [Ta] GUVRBAGPIYLISA-UHFFFAOYSA-N 0.000 claims description 8
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 claims description 7
- ZOKXTWBITQBERF-UHFFFAOYSA-N Molybdenum Chemical compound [Mo] ZOKXTWBITQBERF-UHFFFAOYSA-N 0.000 claims description 7
- VBJZVLUMGGDVMO-UHFFFAOYSA-N hafnium atom Chemical compound [Hf] VBJZVLUMGGDVMO-UHFFFAOYSA-N 0.000 claims description 7
- 239000011733 molybdenum Substances 0.000 claims description 7
- GUCVJGMIXFAOAE-UHFFFAOYSA-N niobium atom Chemical compound [Nb] GUCVJGMIXFAOAE-UHFFFAOYSA-N 0.000 claims description 7
- WFKWXMTUELFFGS-UHFFFAOYSA-N tungsten Chemical compound [W] WFKWXMTUELFFGS-UHFFFAOYSA-N 0.000 claims description 7
- 239000010937 tungsten Substances 0.000 claims description 7
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 claims description 6
- QCWXUUIWCKQGHC-UHFFFAOYSA-N Zirconium Chemical compound [Zr] QCWXUUIWCKQGHC-UHFFFAOYSA-N 0.000 claims description 6
- 239000010703 silicon Substances 0.000 claims description 6
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 claims description 5
- 238000005520 cutting process Methods 0.000 description 36
- 229910045601 alloy Inorganic materials 0.000 description 28
- 239000000956 alloy Substances 0.000 description 28
- 239000000843 powder Substances 0.000 description 26
- XEEYBQQBJWHFJM-UHFFFAOYSA-N iron Substances [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 22
- 239000000203 mixture Substances 0.000 description 15
- 238000003754 machining Methods 0.000 description 13
- 238000002149 energy-dispersive X-ray emission spectroscopy Methods 0.000 description 12
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- 229910001026 inconel Inorganic materials 0.000 description 10
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- 150000001875 compounds Chemical class 0.000 description 6
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- 238000002441 X-ray diffraction Methods 0.000 description 5
- 239000011248 coating agent Substances 0.000 description 5
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- 230000007547 defect Effects 0.000 description 4
- 229910052751 metal Inorganic materials 0.000 description 4
- PXHVJJICTQNCMI-UHFFFAOYSA-N nickel Substances [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 4
- -1 TiC Chemical class 0.000 description 3
- 239000002826 coolant Substances 0.000 description 3
- 239000013078 crystal Substances 0.000 description 3
- 239000012895 dilution Substances 0.000 description 3
- 238000010790 dilution Methods 0.000 description 3
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- 229910052742 iron Inorganic materials 0.000 description 3
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- 238000007088 Archimedes method Methods 0.000 description 2
- XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 description 2
- 230000002159 abnormal effect Effects 0.000 description 2
- 239000011324 bead Substances 0.000 description 2
- 238000005452 bending Methods 0.000 description 2
- 230000003197 catalytic effect Effects 0.000 description 2
- 238000007772 electroless plating Methods 0.000 description 2
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- 239000011888 foil Substances 0.000 description 2
- 239000003966 growth inhibitor Substances 0.000 description 2
- 238000005259 measurement Methods 0.000 description 2
- 150000001247 metal acetylides Chemical class 0.000 description 2
- 229910052759 nickel Inorganic materials 0.000 description 2
- 230000000737 periodic effect Effects 0.000 description 2
- 230000000704 physical effect Effects 0.000 description 2
- 238000004445 quantitative analysis Methods 0.000 description 2
- 238000012360 testing method Methods 0.000 description 2
- 229910052720 vanadium Inorganic materials 0.000 description 2
- GPPXJZIENCGNKB-UHFFFAOYSA-N vanadium Chemical compound [V]#[V] GPPXJZIENCGNKB-UHFFFAOYSA-N 0.000 description 2
- 229910018072 Al 2 O 3 Inorganic materials 0.000 description 1
- ZOXJGFHDIHLPTG-UHFFFAOYSA-N Boron Chemical compound [B] ZOXJGFHDIHLPTG-UHFFFAOYSA-N 0.000 description 1
- PMVSDNDAUGGCCE-TYYBGVCCSA-L Ferrous fumarate Chemical group [Fe+2].[O-]C(=O)\C=C\C([O-])=O PMVSDNDAUGGCCE-TYYBGVCCSA-L 0.000 description 1
- 229910001111 Fine metal Inorganic materials 0.000 description 1
- 229910000883 Ti6Al4V Inorganic materials 0.000 description 1
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 1
- 238000005299 abrasion Methods 0.000 description 1
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- 229910052786 argon Inorganic materials 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 238000000498 ball milling Methods 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 229910052796 boron Inorganic materials 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 238000003763 carbonization Methods 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 238000000151 deposition Methods 0.000 description 1
- 230000008021 deposition Effects 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
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- 230000006872 improvement Effects 0.000 description 1
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- 229910000816 inconels 718 Inorganic materials 0.000 description 1
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- 238000010884 ion-beam technique Methods 0.000 description 1
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- 230000009257 reactivity Effects 0.000 description 1
- 230000001105 regulatory effect Effects 0.000 description 1
- VSZWPYCFIRKVQL-UHFFFAOYSA-N selanylidenegallium;selenium Chemical compound [Se].[Se]=[Ga].[Se]=[Ga] VSZWPYCFIRKVQL-UHFFFAOYSA-N 0.000 description 1
- 239000006104 solid solution Substances 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 238000004544 sputter deposition Methods 0.000 description 1
- 229910052723 transition metal Inorganic materials 0.000 description 1
- 150000003624 transition metals Chemical class 0.000 description 1
- 238000013519 translation Methods 0.000 description 1
Classifications
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- C04B2235/78—Grain sizes and shapes, product microstructures, e.g. acicular grains, equiaxed grains, platelet-structures
- C04B2235/785—Submicron sized grains, i.e. from 0,1 to 1 micron
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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
- C04B2235/78—Grain sizes and shapes, product microstructures, e.g. acicular grains, equiaxed grains, platelet-structures
- C04B2235/786—Micrometer sized grains, i.e. from 1 to 100 micron
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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
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- C04B2235/00—Aspects relating to ceramic starting mixtures or sintered ceramic products
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- C22C26/00—Alloys containing diamond or cubic or wurtzitic boron nitride, fullerenes or carbon nanotubes
- C22C2026/003—Cubic boron nitrides only
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- C22C—ALLOYS
- C22C26/00—Alloys containing diamond or cubic or wurtzitic boron nitride, fullerenes or carbon nanotubes
- C22C2026/005—Alloys containing diamond or cubic or wurtzitic boron nitride, fullerenes or carbon nanotubes with additional metal compounds being borides
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- C22C26/00—Alloys containing diamond or cubic or wurtzitic boron nitride, fullerenes or carbon nanotubes
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- C22C—ALLOYS
- C22C26/00—Alloys containing diamond or cubic or wurtzitic boron nitride, fullerenes or carbon nanotubes
- C22C2026/007—Alloys containing diamond or cubic or wurtzitic boron nitride, fullerenes or carbon nanotubes with additional metal compounds being nitrides
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- C22C26/00—Alloys containing diamond or cubic or wurtzitic boron nitride, fullerenes or carbon nanotubes
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- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C29/00—Alloys based on carbides, oxides, nitrides, borides, or silicides, e.g. cermets, or other metal compounds, e.g. oxynitrides, sulfides
- C22C29/02—Alloys based on carbides, oxides, nitrides, borides, or silicides, e.g. cermets, or other metal compounds, e.g. oxynitrides, sulfides based on carbides or carbonitrides
- C22C29/06—Alloys based on carbides, oxides, nitrides, borides, or silicides, e.g. cermets, or other metal compounds, e.g. oxynitrides, sulfides based on carbides or carbonitrides based on carbides, but not containing other metal compounds
- C22C29/067—Alloys based on carbides, oxides, nitrides, borides, or silicides, e.g. cermets, or other metal compounds, e.g. oxynitrides, sulfides based on carbides or carbonitrides based on carbides, but not containing other metal compounds comprising a particular metallic binder
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- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C29/00—Alloys based on carbides, oxides, nitrides, borides, or silicides, e.g. cermets, or other metal compounds, e.g. oxynitrides, sulfides
- C22C29/02—Alloys based on carbides, oxides, nitrides, borides, or silicides, e.g. cermets, or other metal compounds, e.g. oxynitrides, sulfides based on carbides or carbonitrides
- C22C29/06—Alloys based on carbides, oxides, nitrides, borides, or silicides, e.g. cermets, or other metal compounds, e.g. oxynitrides, sulfides based on carbides or carbonitrides based on carbides, but not containing other metal compounds
- C22C29/08—Alloys based on carbides, oxides, nitrides, borides, or silicides, e.g. cermets, or other metal compounds, e.g. oxynitrides, sulfides based on carbides or carbonitrides based on carbides, but not containing other metal compounds based on tungsten carbide
Definitions
- the present invention relates to a composite sintered body.
- This application claims priority based on Japanese Patent Application No. 2016-206903, which is a Japanese patent application filed on October 21, 2016. All the descriptions described in the Japanese patent application are incorporated herein by reference.
- JP-A-2005-239472 is a high-strength and high-abrasion resistant diamond sintered body comprising sintered diamond particles having an average particle diameter of 2 ⁇ m or less and the remaining binder phase.
- the content of sintered diamond particles in the diamond sintered body is 80% by volume or more and 98% by volume or less, and the content in the binder phase is 0.5% by mass or more and less than 50% by mass, titanium, zirconium, hafnium,
- the binder phase includes at least one element selected from the group consisting of vanadium, niobium, tantalum, chromium, and molybdenum and cobalt having a content in the binder phase of 50% by mass or more and less than 99.5% by mass.
- At least one element selected from the group consisting of titanium, zirconium, hafnium, vanadium, niobium, tantalum, chromium, and molybdenum all exist as carbide particles having an average particle size of 0.8 ⁇ m or less, the structure of the carbide particles is discontinuous, and adjacent sintered diamond particles are bonded to each other. High strength and high wear resistance diamond sintered Disclose the body.
- Patent Document 2 Japanese Patent Application Laid-Open No. 9-316587 includes sintered diamond particles and a binder as the balance, and the sintered diamond particles have a particle size in the range of 0.1 to 4 ⁇ m. Discloses a high-strength fine-grained diamond sintered body containing at least one iron group metal selected from the group consisting of Fe, Co and Ni and having an oxygen content in the range of 0.01 to 0.08% by weight. .
- Patent Document 3 discloses a diamond raw material powder uniformly coated with a transition metal, boron, or silicon of Group 4a, 5a or 6a of periodic table 6 to 0.1% by volume. Disclosed is a diamond sintered body composed of a sintered body obtained by sintering particles at an ultrahigh pressure and a high temperature, containing diamond in a volume of 94 to 99.8%, and the balance being a carbide of the coating material.
- Patent Document 4 discloses a polycrystalline diamond body including a plurality of diamond crystals joined together and a material microstructure including a gap region between the diamond crystals, A titanium-containing particle comprising: a substrate comprising tungsten and a catalytic metal; and a grain growth inhibitor layer comprising a plurality of titanium-containing particles interspersed with tungsten and the catalytic metal between the polycrystalline diamond body and the substrate.
- a size of less than 800 nm the grain growth inhibitor layer is bonded on both sides to the substrate and the polycrystalline diamond body, has a thickness of about 20-100 ⁇ m, and the diamond crystal grain is about 1 ⁇ m or less.
- Disclosed is a polycrystalline diamond compact having an average size.
- Patent Document 5 has a cBN (cubic boron nitride) component of 60% to 95% by volume and a thermal conductivity of 70 W ⁇ m ⁇ 1 ⁇ K ⁇ 1.
- the outermost surface of the above cBN sintered body has at least one element selected from 4a, 5a, 6a group elements and Al, and at least one element selected from C, N, O
- Patent Document 6 is a cubic boron nitride sintered body containing cBN particles and a binder for binding the cBN particles, and 70% by volume to 98% by volume of cBN.
- the particles and the remaining binder are made of a Co compound, an Al compound, WC, and a solid solution thereof.
- the cBN particles in the sintered body have a Mg content of 0.03% by weight or less and a Li content of 0.001% by weight or more and 0.05.
- Disclosed is a cubic boron nitride sintered body containing not more than% by weight.
- JP 2005-239472 A Japanese Patent Laid-Open No. 9-316587 JP-A-1-17836 Special table 2014-531967 gazette International Publication No. 2007/039955 International Publication No. 2005/066381
- a composite sintered body according to the present disclosure includes a plurality of diamond particles having an average particle diameter of 10 ⁇ m or less, a plurality of cubic boron nitride particles having an average particle diameter of 2 ⁇ m or less, and the remaining binder phase. Wherein at least some of the adjacent diamond particles are bonded to each other, the binder phase contains cobalt, and the composite sintered body has a diamond particle content of 30% by volume to 94% by volume, The content of cubic boron nitride particles is 3% by volume or more and 40% by volume or less, and the content of cobalt is 3% by volume or more and 30% by volume or less.
- the diamond sintered body disclosed in (1) is an iron group element (elements of Groups 8, 9, and 10 in the fourth period on the periodic table, that is, iron, cobalt, and nickel 3). The same is true for the following elements.
- the cubic boron nitride (cBN) sintered bodies disclosed in International Publication No. 2007/039955 (Patent Document 5) and International Publication No. 2005/066631 (Patent Document 6) have cBN as a main component thereof in an iron group. It has a low affinity with alloys containing elements and / or titanium, and exhibits high wear resistance even in high-speed machining of heat-resistant alloys formed of alloys containing iron group elements and / or titanium. However, since the cBN sintered body has low fracture resistance, chipping occurs early in high-speed machining of a heat-resistant alloy containing an iron group element and / or titanium, so that a practical life as a tool has not been obtained. .
- an object of the present invention is to provide a composite sintered body that can be applied to high-speed machining of a heat-resistant alloy containing an iron group element and / or titanium and that has both high wear resistance and high fracture resistance by solving the above problems.
- a composite sintered body that can be applied to high-speed processing of a heat-resistant alloy containing an iron group element and / or titanium and has both high wear resistance and high fracture resistance can be provided.
- a composite sintered body includes a plurality of diamond particles having an average particle size of 10 ⁇ m or less, a plurality of cubic boron nitride particles having an average particle size of 2 ⁇ m or less, and the remaining binder phase. And at least a part of adjacent diamond particles are bonded to each other, the binder phase contains cobalt, and the content of diamond particles in the composite sintered body is 30% by volume. It is 94 volume% or less, the content of cubic boron nitride particles is 3 volume% or more and 40 volume% or less, and the content of cobalt is 3 volume% or more and 30 volume% or less.
- the composite sintered body of the present embodiment has both high wear resistance and high fracture resistance.
- the average particle diameter of diamond particles is 2 ⁇ m or less
- the average particle diameter of cubic boron nitride particles is 1 ⁇ m or less
- the content of diamond particles in the composite sintered body Can be 50 volume% or more and 70 volume% or less
- the content rate of cubic boron nitride particles can be 10 volume% or more and 30 volume% or less
- the cobalt content can be 10 volume% or more and 20 volume% or less.
- Such a composite sintered body has high strength and high chipping resistance in addition to high wear resistance and high fracture resistance.
- the binder phase includes at least one element selected from the group consisting of tungsten, titanium, zirconium, hafnium, niobium, tantalum, chromium, aluminum, silicon, and molybdenum. It may further include a chemical component, and in the binder phase, the cobalt content may be 50% by mass or more and 99.5% by mass or less, and the chemical component content may be 0.5% by mass or more and 50% by mass or less. it can.
- Such a composite sintered body has high strength and high chipping resistance in addition to high wear resistance and high fracture resistance.
- At least a part of the chemical component contained in the binder phase is at least one of carbide, carbonitride, nitride, oxide, boride, and oxynitride. can do.
- Such a composite sintered body has both high wear resistance and high fracture resistance, and particularly high wear resistance.
- the thermal conductivity can be set to 100 W ⁇ m ⁇ 1 ⁇ K ⁇ 1 or more.
- Such a composite sintered body is suppressed in temperature rise even in high-speed machining, has both high wear resistance and high fracture resistance, and has a long tool life.
- the composite sintered body of the present embodiment includes a plurality of diamond particles having an average particle diameter of 2 ⁇ m or less, a plurality of cubic boron nitride particles having an average particle diameter of 1 ⁇ m or less, and the remaining binder phase.
- a composite sintered body in which at least part of adjacent diamond particles are bonded to each other, and the binder phase is selected from the group consisting of tungsten, titanium, zirconium, hafnium, niobium, tantalum, chromium, aluminum, silicon, and molybdenum.
- the content of diamond particles is 50 vol% or more and 70 vol% or less, and the inclusion of cubic boron nitride particles
- the rate is 10% by volume or more and 30% by volume or less
- the cobalt content is 10% by volume or more and 20% by volume or less.
- the content ratio of cobalt is 50% by mass or more and 99.5% by mass or less
- the content ratio of the chemical component is 0.5% by mass or more and 50% by mass or less
- at least a part of the chemical component contained in the binder phase is contained.
- Carbide, carbonitride, nitride, oxide, boride and oxynitride, and the thermal conductivity can be 100 W ⁇ m ⁇ 1 ⁇ K ⁇ 1 or more.
- Such a composite sintered body has high chipping resistance in addition to high wear resistance and high fracture resistance, and has a long tool life.
- the composite sintered body according to the present embodiment includes a plurality of diamond particles having an average particle size of 10 ⁇ m or less, a plurality of cubic boron nitride (cBN) particles having an average particle size of 2 ⁇ m or less, and the remaining binder phase.
- the composite sintered body includes at least part of adjacent diamond particles bonded to each other, the binder phase contains cobalt, and the content of the diamond particles in the composite sintered body is 30% by volume or more and 94% by volume. %,
- the content of cubic boron nitride particles is 3% by volume to 40% by volume, and the content of cobalt is 3% by volume to 30% by volume.
- the composite sintered body of the present embodiment has both high wear resistance and high fracture resistance due to the composite of diamond particles and cBN particles.
- the present inventors formed an end mill which is a kind of cutting tool with a cBN sintered body, and when a heat-resistant alloy containing an iron group element (for example, Inconel (registered trademark) 718) was processed, chipping occurred at the cutting edge.
- a heat-resistant alloy containing an iron group element for example, Inconel (registered trademark) 7128
- the cracks generated in the end mill with the cutting edge penetrating the cBN particles.
- the toughness and strength of the cBN particles themselves are insufficient, which is a significant extension on the extension of the conventional cBN sintered body. It turned out that performance improvement cannot be expected.
- the present inventors consider that the cutting distance per blade is short and the cutting edge temperature does not easily rise in high-speed machining of a heat-resistant alloy containing an iron group element and / or titanium by an end mill.
- An end mill was formed from the diamond sintered body, and a heat-resistant alloy containing an iron group element (for example, Inconel (registered trademark) 718) was processed.
- the end mill formed from the diamond sintered body did not generate chipping sporadically by the end mill formed from the cBN sintered body, but has a higher wear rate than the end mill formed from the cBN sintered body. A practical life could not be obtained.
- the present inventors examined the combination of cBN particles having high wear resistance and diamond particles having high fracture resistance.
- the diamond particles having a content suitable for estimating that at least a part of the diamond particles are bonded to each other to form a continuous skeleton structure, and the manufacturing process for forming the skeleton structure, the gap between the skeleton structures is determined.
- the composite sintered body having both high wear resistance and high fracture resistance was successfully obtained by compositing with cBN particles having a content suitable for presuming to be disposed on the surface.
- the average particle diameter of the diamond particles is 10 ⁇ m or less, preferably 2 ⁇ m or less, from the viewpoint of obtaining a high-strength composite sintered body having both high wear resistance and high fracture resistance.
- the average particle diameter of the diamond particles is determined by preparing a cross section arbitrarily specified by the composite sintered body by CP processing using a cross section polisher (CP) apparatus and the like. Dispersive X-ray analysis) is used to identify diamond particles, and assuming that the diamond particles are homogeneously dispersed in the composite sintered body, using image analysis software, the equivalent circle diameter and its average are calculated from the cross-sectional area of each particle. Is calculated as the average particle size.
- the content of the diamond particles in the composite sintered body is 30% by volume or more and 94% by volume or less, preferably from the viewpoint of being suitable for forming a continuous skeleton structure by bonding at least part of the diamond particles to each other. It is 50 volume% or more and 70 volume% or less.
- the content of diamond particles in the composite sintered body is determined by determining the diamond particles by EDX (energy dispersive X-ray analysis) in an arbitrarily specified cross section of the composite sintered body. It is calculated by regarding the area% of the cross-sectional area of the diamond particles as volume% with respect to the total area of the cross-section, assuming that it is uniformly dispersed in the body.
- the continuous skeleton structure formed by bonding at least part of adjacent diamond particles in the composite sintered body is observed with an SEM (scanning electron microscope).
- the average particle diameter of cBN (cubic boron nitride) particles is 2 ⁇ m or less, preferably 1 ⁇ m or less from the viewpoint of obtaining a high-strength composite sintered body having both high wear resistance and high fracture resistance.
- the average particle size of the cBN particles is calculated by the same method as that for diamond particles.
- the content of cBN particles in the composite sintered body is 3% by volume or more and 40% by volume or less, preferably 10% by volume or more, from the viewpoint of being suitable for disposing in the gaps of the skeleton structure formed by the diamond particles. 30% by volume or less.
- the content of the cBN particles in the composite sintered body is determined by determining the cBN particles by EDX (energy dispersive X-ray analysis) in an arbitrarily specified cross section of the composite sintered body. It is calculated by regarding the area% of the cross-sectional area of the cBN particles with respect to the total area of the cross section as volume%, assuming that it is uniformly dispersed in the aggregate.
- EDX energy dispersive X-ray analysis
- the binder phase contains cobalt (Co) from the viewpoint of bonding at least part of adjacent diamond particles to each other.
- the Co content in the composite sintered body is 3% by volume or more and 30% by volume or less, preferably 10% by volume or more and 20% by volume or less, from the viewpoint of bonding at least part of adjacent diamond particles to each other.
- the Co content in the composite sintered body is determined by EDX (energy dispersive X-ray analysis) in an arbitrarily specified cross section of the composite sintered body, and Co is contained in the composite sintered body. It is calculated by regarding the area% of the cross-sectional area discriminated as Co to the total area of the cross-section as volume%.
- the binder phase is tungsten (W), titanium (Ti), zirconium (Zr), hafnium (Hf), niobium (Nb), tantalum (Ta), chromium (Cr). It is preferable to further include a chemical component containing at least one element selected from the group consisting of aluminum (Al), silicon (Si) and molybdenum (Mo). From the viewpoint of increasing the strength of the composite sintered body by bonding at least part of adjacent diamond particles to each other, the Co content in the binder phase is preferably 50% by mass or more and 99.5% by mass or less, and 55% by mass. % To 70% by mass is more preferable.
- At least one selected from the group consisting of the above chemical components W, Ti, Zr, Hf, Nb, Ta, Cr, Al, Si and Mo in the binder phase
- the content of the chemical component containing the above elements is preferably 0.5% by mass or more and 50% by mass or less, and more preferably 30% by mass or more and 45% by mass or less.
- the content of Co and the above chemical components in the binder phase is determined by chemical treatment with Co measured by EDX (energy dispersive X-ray analysis) quantitative analysis by CP treatment of arbitrarily specified cross sections of the composite sintered body. Calculated by taking the mass ratio with the component.
- At least a part of the chemical component including one or more elements is preferably at least one of carbide, carbonitride, nitride, oxide, boride, and oxynitride.
- the chemical component including one or more elements includes carbides such as TiC, carbonitrides such as TiCN, nitrides such as TiN, oxides such as Al 2 O 3 , borides such as TiB 2, and oxynitrides such as sialon (SiAlON).
- the type of the chemical component is determined by a diffraction peak pattern of XRD (X-ray diffraction).
- Thermal conductivity From the viewpoint of suppressing the temperature rise of the composite sintered body so that the composite sintered body can be used for high-speed processing of heat-resistant alloys containing iron group elements and / or titanium with a long life,
- the rate is preferably 100 W ⁇ m ⁇ 1 ⁇ K ⁇ 1 or more, and more preferably 120 W ⁇ m ⁇ 1 ⁇ K ⁇ 1 or more.
- the thermal conductivity of the composite sintered body is calculated from the thermal diffusivity and specific heat measured by the laser flash method and the density measured by the Archimedes method.
- the composite sintered body of this embodiment includes a plurality of diamond particles having an average particle diameter of 2 ⁇ m or less, a plurality of cubic boron nitride particles having an average particle diameter of 1 ⁇ m or less, and the remaining binder phase. And at least some of the adjacent diamond particles are bonded to each other, and the bonding phase is at least selected from the group consisting of W, Ti, Zr, Hf, Nb, Ta, Cr, Al, Si, and Mo.
- the content of diamond particles is 50% by volume or more and 70% by volume or less
- the content of cubic boron nitride particles is a chemical component containing one or more elements and Co.
- the cobalt content is 10 to 20% by volume
- the cobalt content is 50 to 99.5% by mass.
- the chemical component content is 0.5% by mass or more and 50% by mass or less
- at least a part of the chemical component contained in the binder phase is carbide, carbonitride, nitride, oxide, boride. And / or oxynitride, and preferably has a thermal conductivity of 100 W ⁇ m ⁇ 1 ⁇ K ⁇ 1 or higher.
- Such a composite sintered body has high chipping resistance in addition to high wear resistance and high fracture resistance, and has a long tool life.
- the method for producing the composite sintered body according to this embodiment is not particularly limited, but from the viewpoint of efficiently producing the composite sintered body of this embodiment, Co is applied to at least a part of the surface of each particle of the diamond powder.
- a first step of forming a binder-coated diamond powder by coating with a binder a second step of forming a mixture by mixing the binder-coated diamond powder and the cBN powder, and sintering the mixture
- a third step of forming a composite sintered body is not particularly limited, but from the viewpoint of efficiently producing the composite sintered body of this embodiment, Co is applied to at least a part of the surface of each particle of the diamond powder.
- a binder-coated diamond powder is formed by coating at least a part of the surface of each particle of the diamond powder with a binder containing Co.
- the composite sintered body of the present embodiment is obtained by sintering the mixture of the binder-coated diamond powder and the cBN powder in a subsequent process.
- the average particle diameter of the diamond powder used in the first step is not particularly limited, but is 10 ⁇ m or less from the viewpoint of forming a composite sintered body having high strength and high wear resistance and high fracture resistance. Preferably it is 2 micrometers or less.
- the method of coating the binder containing Co on at least a part of the surface of each particle of the diamond powder is not particularly limited, but from the viewpoint of uniform coating with few impurities, electroless plating, arc deposition, powder sputtering The method is preferred. From the viewpoint of forming a composite sintered body having high strength and high wear resistance and high fracture resistance, the binder is W, Ti, Zr, Hf, Nb, Ta, Cr, Al, in addition to Co. It is preferable to include a chemical component containing at least one element selected from the group consisting of Si and Mo. The binder forms a binder phase in the composite sintered body by a subsequent process.
- the mixture is formed by mixing the binder-coated diamond powder and the cBN powder.
- the composite sintered body of the present embodiment is obtained by sintering the mixture in a subsequent process.
- a binder can be added in this step from the viewpoint of adjusting the amount of the binder in the sintered body.
- the first step can be omitted, but it is preferable that the first step is present.
- the average particle size of the cBN powder used in the second step is not particularly limited, but is 2 ⁇ m or less from the viewpoint of forming a composite sintered body having high strength and high wear resistance and high fracture resistance. Preferably it is 1 micrometer or less.
- the method for mixing the binder-coated diamond powder and the cBN powder is not particularly limited, but ball mill mixing, bead mill mixing, planetary mill mixing, jet mill mixing and the like are preferable from the viewpoint of efficient and homogeneous mixing. Further, as described above, the binder can also be mixed at this time.
- the amount of the binder-coated diamond powder that is, the amount of the diamond powder and the amount of the binder with respect to the diamond powder
- the amount of the cBN powder, the Co in the binder and the content of the above chemical components a composite sintered body
- the desired content of diamond particles, the desired content of cBN particles and the desired content of Co, and the desired content of Co and the desired content of the chemical components in the binder phase are obtained.
- a composite sintered body is formed by sintering the mixture.
- the conditions for sintering the mixture are not particularly limited, but from the viewpoint of efficiently obtaining the composite sintered body of the present embodiment, the sintering pressure is preferably 4 GPa or more and 10 GPa or less, more preferably 6 GPa or more and 8 GPa or less.
- the sintering temperature is preferably 1400 ° C. or higher and 2000 ° C. or lower, more preferably 1500 ° C. or higher and 1800 ° C. or lower.
- the sintering time is preferably longer, and preferably 15 minutes or longer and 60 minutes or shorter.
- Example I In this example, no. I-1 to No. As shown in I-12, composite sintered bodies with varying average particle diameters and content ratios of diamond particles and cBN particles and binder content ratios were prepared, and hardness, fracture toughness values and thermal conductivity were measured. did. Further, cutting tools were produced from these composite sintered bodies, and the flank wear width of the cutting edge when Inconel (registered trademark) 718 was cut at high speed was measured to evaluate the life.
- the composite sintered body was produced as follows. The surface of each particle of diamond powder having an average particle diameter of 1 ⁇ m was coated with 6% by mass of Co as a binder on the diamond particles by electroless plating. Thereafter, a diamond powder coated with Co and a cBN powder having an average particle diameter of 1 ⁇ m are wet mixed by a ball mill method to prepare a mixture, and vacuum heat treatment is performed at 1200 ° C. for 30 minutes in order to remove gas adhering to the particle surface. did. This mixture was filled in a Ta (tantalum) container in contact with a WC-6% Co cemented carbide disc and Co foil, and a 6 GPa pressure and 1650 ° C. using a belt type ultra high pressure high temperature generator. A composite sintered body was produced by holding and sintering at the temperature of 30 minutes.
- the eutectic melt of WC-6% Co and Co is infiltrated into the composite sintered body from the WC-6% Co cemented carbide disc and Co foil, and sintered. Therefore, the content of diamond particles and cBN particles in the composite sintered body and the composition of the binder phase are slightly different from the charged composition of the mixture. For this reason, the charge composition of the mixture was designed in anticipation of the infiltration of the eutectic melt.
- each particle is discriminated by EDX in the same manner as the content measurement, and the average is calculated by calculating the equivalent circle diameter from the cross-sectional area of each particle using image analysis software (WinROOF manufactured by Mitani Corporation). The particle size was calculated.
- strengths are measured by 50 kgf load using a Vickers hardness meter
- those fracture toughness values are calculated by IF method prescribed
- the thermal diffusivity and specific heat were measured by the laser flash method, the density was measured by the Archimedes method, and the thermal conductivity was calculated. The results are summarized in Table 1.
- a cutting tool composed of RSX12032ES type (milling diameter 32 mm) end mill type cutter and RDET1204M0 type chip was produced using the above-mentioned composite sintered body.
- a disk-shaped Inconel (registered trademark) 718 having a diameter of 95 mm manufactured by Daido Special Metal Co., Ltd., solution / age hardening material, Rockwell hardness HRC44, ASTM (American Society for Materials Testing) E112
- the upper surface of a workpiece having a grain size of 9 as defined in 1) was cut.
- Cutting conditions were a cutting speed Vc of 600 m / min, a feed amount f of 0.15 mm / tooth, a cutting ap of 0.5 mm, a radial cutting ae of 0.12 mm, and a coolant: WET (20-fold dilution of emulsion). .
- the results are summarized in Table 1.
- the “flank wear and / or chipping width” in Table 1 is the value when the workpiece cutting length is 0.45 m.
- the “life” in Table 1 is the cutting length of the workpiece when the wear of the flank and / or the chipping width exceeds 0.1 mm.
- the cutting tool made of the composite sintered body made of I-11 has no defect on the flank face in high-speed machining of Inconel (registered trademark) 718, which is a heat-resistant alloy formed of an alloy containing an iron group element.
- the width of the flank wear and / or chipping was small, and the life was long regardless of wear or chipping. That is, it comprises diamond particles having an average particle size of 10 ⁇ m or less, cubic boron nitride particles having an average particle size of 2 ⁇ m or less, and the remaining binder phase, and at least some of the adjacent diamond particles are bonded to each other.
- the binder phase contains cobalt, and in the composite sintered body, the content of diamond particles is 30% by volume to 94% by volume, the content of cubic boron nitride particles is 3% by volume to 40% by volume, A composite sintered body having a content of 3% by volume or more and 30% by volume or less has both high wear resistance and high fracture resistance, and a cutting tool formed of such a composite sintered body is formed of an alloy containing iron. Even in the high-speed machining of Inconel (registered trademark) 718, which is a heat-resistant alloy, it has a long life.
- “chipping” indicated by (c) means a minute chippable cut.
- the “defect” shown in Table 1 means a large chip that cannot be cut.
- Example II In this example, no. II-1 to No. As shown in II-12, the binder contains at least one element selected from the group consisting of W, Ti, Zr, Hf, Nb, Ta, Cr, Al, Si and Mo in addition to Co.
- a composite sintered body and a cutting tool were produced in the same manner as in Example I except that chemical components were used, and their physical properties were evaluated.
- the raw material of the chemical component a fine metal powder having an average particle diameter of 2 ⁇ m or less obtained by using an atomizing method was used. No. II-1 to No.
- the formation of these simple substances and compounds was confirmed by XRD of the composite sintered body. XRD was measured in the range of 20 ° to 80 ° using a Cu—K ⁇ ray X-ray light source at a scan step of 0.02 °.
- the composition ratio in the binder phase was calculated by taking the ratio of cobalt to other chemical components using EDX quantitative analysis.
- the cutting conditions were a cutting speed Vc of 300 m / min, a feed amount f of 0.15 mm / blade, a cutting ap of 0.5 mm, a radial cutting ae of 0.12 mm, and a coolant: WET (20 times emulsion dilution). there were.
- the results are summarized in Table 2.
- the “flank wear and / or chipping width” in Table 2 was a value when the workpiece cutting length was 0.45 m.
- “Life” in Table 2 is the cutting length of the workpiece when the flank wear and / or chipping width exceeds 0.1 m.
- TRS bending strength
- the bending strength (TRS) was measured with a span of 4 mm by using a test piece having a length of 6 mm, a width of 3 mm, and a thickness of 0.4 to 0.45 mm of the composite sintered body.
- the cutting tool made of the composite sintered body made of II-11 has no defect on the flank face during high-speed machining of Inconel (registered trademark) 718, which is a heat-resistant alloy formed of an alloy containing an iron group element.
- the width of the flank wear and / or chipping was small, and the life was long regardless of wear or chipping. That is, it comprises diamond particles having an average particle size of 10 ⁇ m or less, cubic boron nitride particles having an average particle size of 2 ⁇ m or less, and the remaining binder phase, and at least some of the adjacent diamond particles are bonded to each other.
- the binder phase contains cobalt, a chemical component containing at least one element selected from the group consisting of W, Ti, Zr, Hf, Nb, Ta, Cr, Al, Si, and Mo, and cobalt.
- the content of diamond particles is 30% by volume to 94% by volume
- the content of cubic boron nitride particles in the composite sintered body is 3% by volume to 40% by volume
- the content of cobalt in the composite sintered body is 3% by volume to 30% by volume
- the cobalt content in the binder phase is 50% by mass to 99.5% by mass
- the chemical component content in the binder phase is 0.5% by mass to 50% by mass.
- the composite sintered body has high wear resistance and high fracture resistance, and the cutting tool formed of such a composite sintered body is a heat-resistant alloy formed of an alloy containing an iron group element. Inconel (registered trademark) Even in high-speed machining of 718, it had a long life.
- Example III in this example, no. III-1 to No. As shown in III-7, a compound of at least one element selected from the group consisting of W, Ti, Zr, Hf, Nb, Ta, Cr, Al, Si, and Mo as a binder A composite sintered body and a cutting tool were prepared and their physical properties were evaluated in the same manner as in Example I except that a chemical component containing was used.
- a chemical component containing was used as the raw material of the above chemical component.
- a compound powder pulverized with beads to an average particle size of about 0.5 ⁇ m was used as the raw material of the above chemical component.
- the cutting conditions were a cutting speed Vc of 800 m / min, a feed amount f of 0.15 mm / tooth, a cutting ap of 0.5 mm, a radial cutting ae of 0.12 mm, and a coolant: WET (20 times emulsion dilution). there were.
- the results are summarized in Table 3.
- the “flank wear and / or chipping width” in Table 3 was a value when the workpiece cutting length was 0.45 m.
- “Life” in Table 3 is the cutting length of the workpiece when the wear of the flank and / or the chipping width exceeds 0.1 m.
- the cutting tool made of the composite sintered body made of III-7 has no defect on the flank surface in high-speed machining of Inconel (registered trademark) 718, which is a heat-resistant alloy formed of an alloy containing an iron group element.
- the width of the flank wear and / or chipping was small, and the life was long regardless of wear or chipping. That is, it comprises diamond particles having an average particle size of 10 ⁇ m or less, cubic boron nitride particles having an average particle size of 2 ⁇ m or less, and the remaining binder phase, and at least some of the adjacent diamond particles are bonded to each other.
- the binder phase is carbide, carbonitride, nitride, oxide, boride of at least one element selected from the group consisting of W, Ti, Zr, Hf, Nb, Ta, Cr, Al, Si and Mo.
- a chemical component containing at least one of oxynitride and cobalt, and the content of diamond particles in the composite sintered body is 30% by volume or more and 94% by volume or less, and the cubic boron nitride particles in the composite sintered body
- the content is 3% by volume to 40% by volume
- the content of cobalt in the composite sintered body is 3% by volume to 30% by volume
- the content of cobalt in the binder phase is 50% by mass to 99.5%.
- a composite sintered body having an amount of not more than% and a chemical component content in the binder phase of not less than 0.5 mass% and not more than 50 mass% has both high wear resistance and high fracture resistance.
- the cutting tool formed in (1) had a long life even in high-speed machining of Inconel (registered trademark) 718, which is a heat-resistant alloy formed of an alloy containing an iron group element.
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Abstract
Description
近年の航空機需要の高まりから、インコネル718(Ni基合金)やTi-6Al-4Vに代表される耐熱合金で構成されるジェットエンジンの主要部品であるタービンディスクやブリスクの高速加工が望まれているが、現状は、超硬工具で切削速度50m/min程度の低速での仕上げ加工がなされており、高速加工という市場の要求を満たす工具は現れていない。
[本開示の効果]
本開示によれば、鉄族元素および/またはチタンを含む耐熱合金の高速加工にも適用可能で、高耐摩耗性および高耐欠損性を兼ね備える複合焼結体を提供できる。
最初に本発明の実施態様を列記して説明する。
<複合焼結体>
本実施形態にかかる複合焼結体は、平均粒径が10μm以下の複数のダイヤモンド粒子と、平均粒径が2μm以下の複数の立方晶窒化ホウ素(cBN)粒子と、残部の結合相と、を備える複合焼結体であって、隣り合うダイヤモンド粒子の少なくとも一部は互いに結合しており、結合相はコバルトを含み、複合焼結体中において、ダイヤモンド粒子の含有率が30体積%以上94体積%以下であり、立方晶窒化ホウ素粒子の含有率が3体積%以上40体積%以下であり、上記コバルトの含有率が3体積%以上30体積%以下である。本実施形態の複合焼結体は、ダイヤモンド粒子とcBN粒子との複合化により、高耐摩耗性および高耐欠損性を兼ね備える。
ダイヤモンド粒子の平均粒径は、高耐摩耗性および高耐欠損性を兼ね備える高強度の複合焼結体を得る観点から、10μm以下であり、好ましくは2μm以下である。ここで、ダイヤモンド粒子の平均粒径は、クロスセクションポリッシャー(CP:Cross section Polisher)装置などを用いたCP加工により複合焼結体の任意に特定される断面を作製し、その断面においてEDX(エネルギー分散型X線分析)によりダイヤモンド粒子を判別し、ダイヤモンド粒子が複合焼結体中に均質に分散しているとして、画像解析ソフトを用いて粒子1個ごとの断面積から円相当径とその平均を算出し、平均粒径とする。
cBN(立方晶窒化ホウ素)粒子の平均粒径は、高耐摩耗性および高耐欠損性を兼ね備える高強度の複合焼結体を得る観点から、2μm以下であり、好ましくは1μm以下である。ここで、cBN粒子の平均粒径は、ダイヤモンド粒子と同様の方法で算出する。複合焼結体中におけるcBN粒子の含有率は、ダイヤモンド粒子により形成される上記スケルトン構造の隙間に配置するのに適する観点から、3体積%以上40体積%以下であり、好ましくは10体積%以上30体積%以下である。ここで、複合焼結体中におけるcBN粒子の含有率は、複合焼結体の任意に特定される断面において、EDX(エネルギー分散型X線分析)によりcBN粒子を判別し、cBN粒子が複合焼結体中に均質に分散しているとして、その断面の全面積に対するcBN粒子の断面積の面積%を体積%とみなすことにより算出する。
結合相は、隣り合うダイヤモンド粒子の少なくとも一部を互いに結合させる観点から、コバルト(Co)を含む。複合焼結体中におけるCoの含有率は、隣り合うダイヤモンド粒子の少なくとも一部を互いに結合させる観点から、3体積%以上30体積以下であり、好ましくは10体積%以上20体積%以下である。ここで、複合焼結体中におけるCoの含有率は、複合焼結体の任意に特定される断面において、EDX(エネルギー分散型X線分析)によりCoを判別し、Coが複合焼結体中に均質に分散しているとして、その断面の全面積に対するCoと判別される断面積の面積%を体積%とみなすことにより算出する。
鉄族元素および/またはチタンを含む耐熱合金の高速加工に複合焼結体を長寿命で用いることができるように、複合焼結体の温度上昇を抑制する観点から、複合焼結体の熱伝導率は、100W・m-1・K-1以上が好ましく、120W・m-1・K-1以上がより好ましい。ここで、複合焼結体の熱伝導率は、レーザフラッシュ法により測定される熱拡散率および比熱と、アルキメデス法により測定される密度と、により算出する。
本実施形態にかかる複合焼結体の製造方法は、特に制限がないが、本実施形態の複合焼結体を効率よく製造する観点から、ダイヤモンド粉末の各粒子の表面の少なくとも一部にCoを含む結合材を被覆することにより結合材被覆ダイヤモンド粉末を形成する第1工程と、結合材被覆ダイヤモンド粉末とcBN粉末とを混合することにより混合物を形成する第2工程と、混合物を焼結することにより複合焼結体を形成する第3工程と、を備えることが好ましい。
第1工程において、ダイヤモンド粉末の各粒子の表面の少なくとも一部にCoを含む結合材を被覆することにより結合材被覆ダイヤモンド粉末を形成する。結合材被覆ダイヤモンド粉末とcBN粉末との混合物を後工程で焼結することにより、本実施形態の複合焼結体が得られる。
第2工程において、結合材被覆ダイヤモンド粉末とcBN粉末とを混合することにより混合物を形成する。かかる混合物を後工程で焼結することにより、本実施形態の複合焼結体が得られる。また、焼結体中の結合材量を調整する観点から本工程で結合材を添加することもできる。第2工程で結合材を添加する場合は、第1工程を省略することもできるが、第1工程があることが好ましい。
第3工程において、混合物を焼結することにより複合焼結体を形成する。混合物を焼結する条件は、特に制限はないが、効率よく本実施形態の複合焼結体を得る観点から、焼結圧力が好ましくは4GPa以上10GPa以下であり、より好ましくは6GPa以上8GPa以下であり、焼結温度が好ましくは1400℃以上2000℃以下であり、より好ましくは1500℃以上1800℃以下である。ダイヤモンド粒子のスケルトン構造を形成するためには焼結時間は長いほうが好ましく、15分以上60分以下が好ましい。通常、微粒のダイヤモンド粒子を6GPa以上および1500℃以上の高圧高温で長時間焼結すると異常粒成長が生じるが、本実施形態ではcBN粒子をダイヤモンド格子間に配することで異常粒成長を抑制し、従来より長時間での焼結が可能となる。
本実施例は、表1のNo.I-1~No.I-12に示すように、ダイヤモンド粒子およびcBN粒子の平均粒径と含有率、ならびに結合材の含有率を変化させた複合焼結体を作製し、硬度、破壊靭性値および熱伝導率を測定した。さらに、それらの複合焼結体で切削工具を作製して、インコネル(登録商標)718を高速切削したときの刃先の逃げ面摩耗幅を測定し、寿命を評価した。
本実施例は、表2のNo.II-1~No.II-12に示すように、結合材として、Coに加えて、W、Ti、Zr、Hf、Nb、Ta、Cr、Al、SiおよびMoからなる群より選ばれる少なくとも1種以上の元素を含む化学成分を用いたこと以外は、実施例Iと同様にして、複合焼結体および切削工具を作製して、それらの物性を評価した。ここで、上記の化学成分の原料は、アトマイズ法を用いて得られた平均粒径が2μm以下の微粒金属粉末を用いた。No.II-1~No.II-12で作製した複合焼結体の結合相中には、W、Ti、Zr、Hf、Nb、Ta、Cr、Al、SiおよびMoからなる群より選ばれる少なくとも1種以上の元素の単体もしくはCoとの合金、それらの炭化物、ホウ化物、窒化物、炭窒化物、酸化物、および酸窒化物などが形成されていた。これらの単体および化合物の形成は、複合焼結体のXRDにより確認した。XRDは、Cu-Kα線のX線光源を用いて20°~80°の範囲で、スキャンステップ0.02°で測定した。結合相中の組成比率はEDXの定量分析を用いてコバルトとその他の化学成分との比をとることで算出した。
本実施例は、表3のNo.III-1~No.III-7に示すように、結合材として、Coに加えて、W、Ti、Zr、Hf、Nb、Ta、Cr、Al、SiおよびMoからなる群より選ばれる少なくとも1種以上の元素の化合物を含む化学成分を用いたこと以外は、実施例Iと同様にして、複合焼結体および切削工具を作製して、それらの物性を評価した。ここで、上記の化学成分の原料は、平均粒径が0.5μm程度までビーズミル粉砕した化合物粉末を用いた。
Claims (6)
- 平均粒径が10μm以下の複数のダイヤモンド粒子と、平均粒径が2μm以下の複数の立方晶窒化ホウ素粒子と、残部の結合相と、を備える複合焼結体であって、
隣り合う前記ダイヤモンド粒子の少なくとも一部は互いに結合しており、
前記結合相はコバルトを含み、
前記複合焼結体中において、前記ダイヤモンド粒子の含有率が30体積%以上94体積%以下であり、前記立方晶窒化ホウ素粒子の含有率が3体積%以上40体積%以下であり、前記コバルトの含有率が3体積%以上30体積%以下である複合焼結体。 - 前記ダイヤモンド粒子の平均粒径が2μm以下であり、前記立方晶窒化ホウ素粒子の平均粒径が1μm以下であり、
前記複合焼結体中において、前記ダイヤモンド粒子の含有率が50体積%以上70体積%以下であり、前記立方晶窒化ホウ素粒子の含有率が10体積%以上30体積%以下であり、前記コバルトの含有率が10体積%以上20体積%以下である請求項1に記載の複合焼結体。 - 前記結合相は、タングステン、チタン、ジルコニウム、ハフニウム、ニオブ、タンタル、クロム、アルミニウム、シリコンおよびモリブデンからなる群より選ばれる少なくとも1種以上の元素を含む化学成分をさらに含み、
前記結合相中において、前記コバルトの含有率が50質量%以上99.5質量%以下であり、前記化学成分の含有率が0.5質量%以上50質量%以下である請求項1または請求項2に記載の複合焼結体。 - 前記結合相中に含まれる前記化学成分の少なくとも一部は、炭化物、炭窒化物、窒化物、酸化物、ホウ化物および酸窒化物の少なくともいずれかである請求項1から請求項3のいずれか1項に記載の複合焼結体。
- 熱伝導率が100W・m-1・K-1以上である請求項1から請求項4のいずれか1項に記載の複合焼結体。
- 平均粒径が2μm以下の複数のダイヤモンド粒子と、平均粒径が1μm以下の複数の立方晶窒化ホウ素粒子と、残部の結合相と、を備える複合焼結体であって、
隣り合う前記ダイヤモンド粒子の少なくとも一部は互いに結合しており、
前記結合相は、タングステン、チタン、ジルコニウム、ハフニウム、ニオブ、タンタル、クロム、アルミニウム、シリコンおよびモリブデンからなる群より選ばれる少なくとも1種以上の元素を含む化学成分と、コバルトと、を含み、
前記複合焼結体中において、前記ダイヤモンド粒子の含有率が50体積%以上70体積%以下であり、前記立方晶窒化ホウ素粒子の含有率が10体積%以上30体積%以下であり、前記コバルトの含有率が10体積%以上20体積%以下であり、
前記結合相中において、前記コバルトの含有率が50質量%以上99.5質量%以下であり、前記化学成分の含有率が0.5質量%以上50質量%以下であり、
前記結合相中に含まれる前記化学成分の少なくとも一部は、炭化物、炭窒化物、窒化物、酸化物、ホウ化物および酸窒化物の少なくともいずれかであり、
熱伝導率が100W・m-1・K-1以上である複合焼結体。
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EP (1) | EP3530767A4 (ja) |
JP (1) | JPWO2018074275A1 (ja) |
KR (1) | KR20190073370A (ja) |
CN (1) | CN109890991A (ja) |
MX (1) | MX2019004560A (ja) |
WO (1) | WO2018074275A1 (ja) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
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WO2021161911A1 (ja) * | 2020-02-13 | 2021-08-19 | 株式会社ダイセル | 金属組成物 |
Families Citing this family (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP6775694B2 (ja) * | 2018-04-24 | 2020-10-28 | 住友電気工業株式会社 | 複合焼結体 |
CN114214552A (zh) * | 2021-12-02 | 2022-03-22 | 广东工业大学 | 一种金刚石制品及其制造方法 |
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JPS6240340A (ja) * | 1985-08-14 | 1987-02-21 | Mitsubishi Metal Corp | 切削工具用ダイヤモンド系焼結材料 |
JPS6415343A (en) * | 1987-07-07 | 1989-01-19 | Sumitomo Electric Industries | Heat-resistant composite sintered compact and its production |
JPH0421568A (ja) * | 1990-05-15 | 1992-01-24 | Kobe Steel Ltd | 高硬度微細結晶焼結体及びその製造方法 |
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JPH04300106A (ja) * | 1991-03-28 | 1992-10-23 | Mitsubishi Materials Corp | 硬質相密着性のすぐれた超高圧焼結材料製切削工具 |
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JPS5823353B2 (ja) * | 1978-05-17 | 1983-05-14 | 住友電気工業株式会社 | 切削工具用焼結体とその製造法 |
JPS5622676A (en) * | 1979-07-26 | 1981-03-03 | Kuratomi Tatsuro | Diamond cubic boron nitride composite solidifed body and its manufacture |
JPS5673668A (en) * | 1979-11-21 | 1981-06-18 | Kuratomi Tatsuro | Diamond cubic boron nitride composite solificated body and its manufacture |
JPH066769B2 (ja) | 1987-07-10 | 1994-01-26 | 工業技術院長 | ダイヤモンド焼結体及びその製造法 |
JPH05132704A (ja) * | 1991-11-11 | 1993-05-28 | Kobe Steel Ltd | 高硬度微細結晶焼結体およびその製造方法 |
JP4297987B2 (ja) | 1996-05-29 | 2009-07-15 | 住友電工ハードメタル株式会社 | 高強度微粒ダイヤモンド焼結体およびそれを用いた工具 |
US7524785B2 (en) | 2004-01-08 | 2009-04-28 | Sumitomo Electric Hardmetal Corp. | Cubic boron nitride sintered body |
JP4542799B2 (ja) * | 2004-02-25 | 2010-09-15 | 住友電工ハードメタル株式会社 | 高強度・高耐摩耗性ダイヤモンド焼結体およびその製造方法 |
CA2577615C (en) | 2005-10-04 | 2013-02-05 | Satoru Kukino | Cbn sintered body for high surface integrity machining and cbn sintered body cutting tool |
JP5658422B2 (ja) | 2011-08-23 | 2015-01-28 | エレメント シックス リミテッド | ダイヤモンドと基板との間に結晶粒成長阻止剤層を有する微細な多結晶質ダイヤモンドコンパクト |
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2017
- 2017-10-10 JP JP2018546260A patent/JPWO2018074275A1/ja active Pending
- 2017-10-10 KR KR1020197010835A patent/KR20190073370A/ko unknown
- 2017-10-10 EP EP17861577.9A patent/EP3530767A4/en not_active Withdrawn
- 2017-10-10 CN CN201780064627.5A patent/CN109890991A/zh active Pending
- 2017-10-10 MX MX2019004560A patent/MX2019004560A/es unknown
- 2017-10-10 WO PCT/JP2017/036588 patent/WO2018074275A1/ja active Application Filing
- 2017-10-10 US US16/343,695 patent/US20190271062A1/en not_active Abandoned
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JPS6415343A (en) * | 1987-07-07 | 1989-01-19 | Sumitomo Electric Industries | Heat-resistant composite sintered compact and its production |
JPH0421568A (ja) * | 1990-05-15 | 1992-01-24 | Kobe Steel Ltd | 高硬度微細結晶焼結体及びその製造方法 |
JPH04300105A (ja) * | 1991-03-28 | 1992-10-23 | Mitsubishi Materials Corp | 硬質相密着性のすぐれた超高圧焼結材料製切削工具 |
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WO2021161911A1 (ja) * | 2020-02-13 | 2021-08-19 | 株式会社ダイセル | 金属組成物 |
Also Published As
Publication number | Publication date |
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MX2019004560A (es) | 2019-08-05 |
CN109890991A (zh) | 2019-06-14 |
KR20190073370A (ko) | 2019-06-26 |
EP3530767A1 (en) | 2019-08-28 |
US20190271062A1 (en) | 2019-09-05 |
EP3530767A4 (en) | 2020-03-04 |
JPWO2018074275A1 (ja) | 2019-08-22 |
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