USRE41646E1 - Cemented carbide body with increased wear resistance - Google Patents

Cemented carbide body with increased wear resistance Download PDF

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Publication number
USRE41646E1
USRE41646E1 US11/484,834 US48483497A USRE41646E US RE41646 E1 USRE41646 E1 US RE41646E1 US 48483497 A US48483497 A US 48483497A US RE41646 E USRE41646 E US RE41646E
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United States
Prior art keywords
grain size
grains
ratio
group
cemented carbide
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Expired - Lifetime
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US11/484,834
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English (en)
Inventor
Ake Ostlund
Mats Waldenstrom
Ove Alm
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Sandvik Intellectual Property AB
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Sandvik Intellectual Property AB
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Priority claimed from PCT/SE1997/001242 external-priority patent/WO1998003690A1/en
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Publication of USRE41646E1 publication Critical patent/USRE41646E1/en
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Classifications

    • GPHYSICS
    • G01MEASURING; TESTING
    • G01MTESTING STATIC OR DYNAMIC BALANCE OF MACHINES OR STRUCTURES; TESTING OF STRUCTURES OR APPARATUS, NOT OTHERWISE PROVIDED FOR
    • G01M11/00Testing of optical apparatus; Testing structures by optical methods not otherwise provided for
    • G01M11/30Testing of optical devices, constituted by fibre optics or optical waveguides
    • G01M11/37Testing of optical devices, constituted by fibre optics or optical waveguides in which light is projected perpendicularly to the axis of the fibre or waveguide for monitoring a section thereof
    • GPHYSICS
    • G02OPTICS
    • G02BOPTICAL ELEMENTS, SYSTEMS OR APPARATUS
    • G02B6/00Light guides; Structural details of arrangements comprising light guides and other optical elements, e.g. couplings
    • G02B6/24Coupling light guides
    • G02B6/255Splicing of light guides, e.g. by fusion or bonding
    • G02B6/2551Splicing of light guides, e.g. by fusion or bonding using thermal methods, e.g. fusion welding by arc discharge, laser beam, plasma torch

Definitions

  • the present invention relates to coated cemented carbide bodies particularly useful in tools for turning, milling and drilling of steels and stainless steels.
  • Cemented carbide bodies are manufactured according to powder metallurgical methods including milling, pressing and sintering.
  • the milling operation is an intensive mechanical milling in mills of different sizes and with the aid of milling bodies.
  • the milling time is of the order of several hours up to days. Such processing is believed to be necessary in order to obtain a uniform distribution of the binder phase in the milled mixture, but it results in a wide WC grain size distribution.
  • It is an aspect of this invention to provide a method of making a cemented carbide body comprising wet mixing without milling of at least two different WC-powders with deagglomerated powders of other carbides, binder metal and pressing agent such that the WC-powders are coated with the binder phase, said WC-grains being carefully deagglomerated before and after being coated with binder metal, the grains of the WC-powder being classified in at least two groups in which a group of smaller grains has a maximum grain size a max and a group of a larger grains has a minimum grain size b min , each group containing at least 10% of the total amount of WC grains wherein b min ⁇ a max >0.5 mm, the variation in grain size within each group being >1 ⁇ m, drying said mixture, pressing to a desired shape and sintering said pressed bodies.
  • the present invention relates generally to a cemented carbide body comprising WC with an average grain size of ⁇ 10 ⁇ m in a binder phase.
  • the WC grains are classified in at least two groups in which a group of smaller grains has a maximum grain size a max and a group of larger grains has a minimum grain size b min .
  • Each group contains at least 10% of the total amount of WC grains.
  • the cemented carbide body according to the invention is characterized in that b min ⁇ a max >0.5 ⁇ m and that the variation in grain size within each group is >1 ⁇ m.
  • the WC grains have a narrow bimodal grain size distribution with grain sizes in the ranges 0-1.5 ⁇ m and 2.5-6.0 ⁇ m respectively, and with a weight ratio of fine WC particles (0-1.5 ⁇ m) to coarse WC particles (2.5-6.0 ⁇ m) in the range of 0.25-4.0, preferably 0.5-2.0.
  • the amount of W dissolved in the binder phase is controlled by adjustment of the carbon content by small additions of carbon black or pure tungsten powder.
  • the CW-value in inserts according to the invention shall be 0.82-1.0, preferably 0.86-0.96.
  • a cemented carbide body comprising wet mixing without milling of at least two different WC-powders with deagglomerated powders of other carbides, generally TiC, TaC and/or NbC, binder metal and pressing agent, dried preferably by spray drying, pressed to inserts and sintered.
  • the grains of the WC-powder are classified in at least two groups in which a group of smaller grains has a maximum grain size a max and a group of larger grains has a minimum grain size b min each group containing at least 10% of the total amount of WC grains wherein b min ⁇ a max >0.5 ⁇ m and the variation in grain size within each group is >1 ⁇ m.
  • the WC grains are carefully deagglomerated before and after being coated with binder metal.
  • WC-powders with two narrow grain size distributions of 0-1.5 ⁇ m and 2.5-6.0 ⁇ m respectively and a weight ratio of fine WC particles (0-1.5 ⁇ m) to coarse WC particles (2.5-6.0 ⁇ m) in the range of 0.25-4.0, preferably 0.5-2.0 are wet mixed without milling with other carbides generally TiC, TaC and/or NbC, binder metal and pressing agent, dried preferably by spray drying, pressed to inserts and sintered.
  • Cemented carbide tool inserts of the type SEMN 1204 AZ, an insert for milling, with the composition in addition to WC of 8.4 wt % Co, 1.13 wt % TaC and 0.38 wt % NbC were produced according to the invention.
  • Cobalt coated WC, WC-6 wt-% Co, prepared in accordance with U.S. Pat. No. 5,505,902 was carefully deagglomerated in a laboratory jetmill equipment, mixed with additional amounts of Co and deagglomerated uncoated (Ta,Nb)C and TaC powders to obtain the desired material composition.
  • the coated WC-particles consisted of 50 wt % with an average grain size of 3.5 ⁇ m and 50 wt % with 1.2 ⁇ m average grain size, giving a bimodal grain size distribution.
  • the mixing was carried out in an ethanol and water solution (0.25 l fluid per kg cemented carbide powder) for 2 hours in a laboratory mixer and the batch size was 10 kg. Furthermore, 2 weight-% lubricant, was added to the slurry.
  • the carbon content was adjusted with carbon black to a binder phase alloyed with W corresponding to a CW-ratio of 0.89. After spray drying, the inserts were pressed and sintered according to standard practise and dense structures with no porosity were obtained.
  • the inserts were coated with a 0.5 ⁇ m equiaxed TiCN-layer (with a high nitrogen content corresponding to an estimated C/N-ratio of 0.05) followed by a 4 ⁇ m thick TiCN-layer with columnar grains by using the MTCVD-technique (temperature 885-850° C. and CH 3 CN as the carbon and nitrogen sources).
  • a 1.0 ⁇ m thick layer of Al 2 O 3 was deposited using a temperature 970° C. and a concentration of H 2 S dopant of 0.4% as disclosed in EP-A-523 021.
  • a thin (0.3 ⁇ m) layer of TiN was deposited on top according to known CVD-technique. XRD-measurement showed that the Al 2 O 3 -layer consisted of 100% ⁇ -phase.
  • the coated inserts were brushed by a nylon straw brush containing SiC grains. Examination of the brushed inserts in a light microscope showed that the thin TiN-layer had been brushed away only along the cutting edge leaving there a smooth Al 2 O 3 -layer surface.
  • Coating thickness measurements on cross sectioned brush samples showed no reduction of the coating along the edge line except for the outer TiN-layer that was removed.
  • Cemented carbide tool inserts of the type SEMN 1204 AZ, an insert for milling, with the composition 9.1 wt % Co, 1.23 wt % TaC and 0.30 wt % NbC and the rest WC with unimodal distribution and an average grain size of 1.2 ⁇ m were produced in the following way.
  • Cobalt coated WC, WC-6 weight-% Co, prepared in accordance with U.S. Pat. No. 5,505,902 was carefully deagglomerated in a laboratory jetmill equipment, mixed with additional amounts of Co and deagglomerated uncoated (Ta,Nb)C and TaC powders to obtain the desired material composition.
  • the mixing was carried out in an ethanol and water solution (0.25 l fluid per kg cemented carbide powder) for 2 hours in a laboratory mixer and the batch size was 10 kg. Furthermore, 2 weight-% lubricant, was added to the slurry. The carbon content was adjusted with carbon black to a binder phase highly alloyed with W corresponding to a CW-ratio of 0.89. After spray drying, the inserts were pressed and sintered according to standard practise and dense structures with no porosity were obtained.
  • the inserts were coated in the same coating batch as the inserts A above.
  • the coated inserts were brushed by a nylon straw brush containing SiC grains. Examination of the brushbed inserts in a light microscope showed that the thin TiN-layer had been brushed away only along the cutting edge leaving there a smooth Al 2 O 3 -layer surface.
  • Coating thickness measurements on cross sectioned brushed samples showed no reduction of the coating along the edge line except for the outer TiN-layer that was removed.
  • Two parallel bars each of a thickness of 35 mm were centrally positioned relative the cutter body (diameter 100 mm ), and the bars were placed with an air gap of 10 mm between them.
  • the cutting data were:

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  • Physics & Mathematics (AREA)
  • Optics & Photonics (AREA)
  • General Physics & Mathematics (AREA)
  • Engineering & Computer Science (AREA)
  • Plasma & Fusion (AREA)
  • Chemical & Material Sciences (AREA)
  • Analytical Chemistry (AREA)
  • Mechanical Coupling Of Light Guides (AREA)
  • Length Measuring Devices By Optical Means (AREA)
  • Cutting Tools, Boring Holders, And Turrets (AREA)
  • Powder Metallurgy (AREA)
US11/484,834 1996-07-19 1997-07-08 Cemented carbide body with increased wear resistance Expired - Lifetime USRE41646E1 (en)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
SE9602821A SE511817C2 (sv) 1996-07-19 1996-07-19 Förfarande och anordning för att bestämma vinkelläget för minst en axiell optisk asymmetri, samt användning av förfarandet respektive anordningen
SE9602821 1996-07-19
PCT/SE1997/001242 WO1998003690A1 (en) 1996-07-19 1997-07-08 Cemented carbide body with increased wear resistance

Related Parent Applications (1)

Application Number Title Priority Date Filing Date
US09/214,924 Reissue US6210632B1 (en) 1996-07-19 1997-07-08 Cemented carbide body with increased wear resistance

Publications (1)

Publication Number Publication Date
USRE41646E1 true USRE41646E1 (en) 2010-09-07

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Family Applications (2)

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US11/484,834 Expired - Lifetime USRE41646E1 (en) 1996-07-19 1997-07-08 Cemented carbide body with increased wear resistance
US08/895,573 Expired - Lifetime US5850283A (en) 1996-07-19 1997-07-16 Determination of angular position of weak axial asymmetries of optical fibers and alignment of and splicing fibers

Family Applications After (1)

Application Number Title Priority Date Filing Date
US08/895,573 Expired - Lifetime US5850283A (en) 1996-07-19 1997-07-16 Determination of angular position of weak axial asymmetries of optical fibers and alignment of and splicing fibers

Country Status (5)

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US (2) USRE41646E1 (de)
EP (1) EP0819958B1 (de)
JP (1) JPH10307227A (de)
DE (1) DE69738121T2 (de)
SE (1) SE511817C2 (de)

Families Citing this family (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
SE511805C2 (sv) * 1997-02-14 1999-11-29 Ericsson Telefon Ab L M Förfarande och anordning för bestämning av hopsmältningsström för hopsvetsning av optiska fibrer, samt användning av förfarandet respektive anordningen
US6721467B2 (en) 2001-06-07 2004-04-13 3M Innovative Properties Company Method and apparatus for aligning the polarization of a polarization maintaining optical fiber to the polarization of a light source
SE0200569L (sv) 2002-02-26 2003-10-23 Ericsson Telefon Ab L M Inriktning av PM-fibrer
WO2013003335A1 (en) 2011-06-27 2013-01-03 Vytran, Llc Apparatus and methods for the determination of a birefringence axis of a polarization-maintaining optical fiber
PL3596780T3 (pl) 2017-03-13 2022-01-31 Telefonaktiebolaget Lm Ericsson (Publ) Samokalibracja układu szyku antenowego
EP3857732A1 (de) * 2018-09-28 2021-08-04 Telefonaktiebolaget Lm Ericsson (Publ) Systeme und verfahren zur korrektur der strahlrichtung durch selbstkopplung

Citations (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5505751A (en) 1987-05-28 1996-04-09 Kennametal Inc. Cutting tool
US5505902A (en) 1994-03-29 1996-04-09 Sandvik Ab Method of making metal composite materials
US5529804A (en) 1994-03-31 1996-06-25 Sandvik Ab Method of making metal composite powders
US5593474A (en) 1988-08-04 1997-01-14 Smith International, Inc. Composite cemented carbide
US5624766A (en) 1993-08-16 1997-04-29 Sumitomo Electric Industries, Ltd. Cemented carbide and coated cemented carbide for cutting tool
US5674564A (en) 1991-06-25 1997-10-07 Sandvik Ab Alumina-coated sintered body
US5773735A (en) 1996-11-20 1998-06-30 The Dow Chemical Company Dense fine grained monotungsten carbide-transition metal cemented carbide body and preparation thereof

Family Cites Families (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5013345A (en) * 1987-12-04 1991-05-07 Fujikura Ltd. Method of fusion-splicing polarization maintaining optical fibers
US5323225A (en) * 1992-08-26 1994-06-21 Andrew Corporation Method of determining azimuthal position of transverse axes of optical fibers with elliptical cores
JP3737107B2 (ja) * 1993-11-29 2006-01-18 テレフオンアクチーボラゲツト エル エム エリクソン 光学的な軸非対称性を持つ光ファイバの間の角オフセットの決定とファイバの芯合わせおよび継ぎ合わせ
JP3168844B2 (ja) * 1994-10-13 2001-05-21 住友電気工業株式会社 定偏波光ファイバの融着接続方法
SE506956C2 (sv) * 1995-10-24 1998-03-09 Ericsson Telefon Ab L M Förfarande och anordning för att bestämma vinkelläget för en optisk axiell asymmetri, samt användning av förfarandet respektive anordningen

Patent Citations (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5505751A (en) 1987-05-28 1996-04-09 Kennametal Inc. Cutting tool
US5593474A (en) 1988-08-04 1997-01-14 Smith International, Inc. Composite cemented carbide
US5674564A (en) 1991-06-25 1997-10-07 Sandvik Ab Alumina-coated sintered body
US5624766A (en) 1993-08-16 1997-04-29 Sumitomo Electric Industries, Ltd. Cemented carbide and coated cemented carbide for cutting tool
US5505902A (en) 1994-03-29 1996-04-09 Sandvik Ab Method of making metal composite materials
US5529804A (en) 1994-03-31 1996-06-25 Sandvik Ab Method of making metal composite powders
US5773735A (en) 1996-11-20 1998-06-30 The Dow Chemical Company Dense fine grained monotungsten carbide-transition metal cemented carbide body and preparation thereof

Non-Patent Citations (6)

* Cited by examiner, † Cited by third party
Title
ASM Handbook, vol. 7, Powder Metallurgy, 9th ed., pp. 798801, 1984. *
Derwent WPI, Dialog Accession No. 003687589, WPI Accession No. 83-47567K/198320, (Sumitomo Electric Ind Co), "Impact resistant hard alloy-consists of hexagonal molybdenum tungsten carbide (mixed with tungsten carbide) in iron Gp. metal binder phase", & JP,A,58058245, 19830406, 198320 B. *
Derwent WPI, Dialog Accession No. 007185293, WPI Accession No. 87-182302/198726, (Mitsubishi Metal Corp) "Hot rolling roll of tungsten carbide-based cemented carbide-has excellent toughness and crackling resistance", & JP,A,62112750, 19870523, 198726 B.
Derwent WPI, Dialog Accession No. 008183518, WPI Accession No. 90-070519/199010, (Mitsubishi Metal Corp), "Tungsten carbide base hard alloy end mills-cont. cobalt, nickel, chromium, vanadium, titanium carbide, niobium carbide", & JP,A,2022438, 19900125, 199010 B.
Derwent WPPI, Dialog Accession No. 003687589, WPI Accession No. 83-47567K/198320, (Sumitomo Electric Ind Co), "Impact resistant hard alloy-consists of hexagonal molybdenum tungsten carbide (mixed with tungsten carbide) in iron Gp. metal binder phase", & JP,A,58058245, 19830406, 198320 B.
US 4,966,627, 10/1990, Keshavan et al. (withdrawn)

Also Published As

Publication number Publication date
US5850283A (en) 1998-12-15
SE9602821L (sv) 1998-01-20
EP0819958A1 (de) 1998-01-21
DE69738121D1 (de) 2007-10-25
JPH10307227A (ja) 1998-11-17
SE9602821D0 (sv) 1996-07-19
EP0819958B1 (de) 2007-09-12
SE511817C2 (sv) 1999-11-29
DE69738121T2 (de) 2008-06-12

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