SU963450A3 - Cutting tool - Google Patents

Cutting tool Download PDF

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SU963450A3
SU963450A3 SU721848420A SU1848420A SU963450A3 SU 963450 A3 SU963450 A3 SU 963450A3 SU 721848420 A SU721848420 A SU 721848420A SU 1848420 A SU1848420 A SU 1848420A SU 963450 A3 SU963450 A3 SU 963450A3
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USSR - Soviet Union
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layer
hard alloy
carbide
titanium carbide
substrate
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SU721848420A
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Russian (ru)
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Нильс Линдстрем Ян
Ионсон Бофолке
Иоган Олоф Вильям Олссон Фол
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Сондвик Актиеболаг (Фирма)
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    • C23COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
    • C23CCOATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
    • C23C16/00Chemical coating by decomposition of gaseous compounds, without leaving reaction products of surface material in the coating, i.e. chemical vapour deposition [CVD] processes
    • C23C16/22Chemical coating by decomposition of gaseous compounds, without leaving reaction products of surface material in the coating, i.e. chemical vapour deposition [CVD] processes characterised by the deposition of inorganic material, other than metallic material
    • C23C16/30Deposition of compounds, mixtures or solid solutions, e.g. borides, carbides, nitrides
    • C23C16/34Nitrides
    • CCHEMISTRY; METALLURGY
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    • C23CCOATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
    • C23C16/00Chemical coating by decomposition of gaseous compounds, without leaving reaction products of surface material in the coating, i.e. chemical vapour deposition [CVD] processes
    • C23C16/22Chemical coating by decomposition of gaseous compounds, without leaving reaction products of surface material in the coating, i.e. chemical vapour deposition [CVD] processes characterised by the deposition of inorganic material, other than metallic material
    • C23C16/30Deposition of compounds, mixtures or solid solutions, e.g. borides, carbides, nitrides
    • C23C16/32Carbides
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    • C23C16/00Chemical coating by decomposition of gaseous compounds, without leaving reaction products of surface material in the coating, i.e. chemical vapour deposition [CVD] processes
    • C23C16/22Chemical coating by decomposition of gaseous compounds, without leaving reaction products of surface material in the coating, i.e. chemical vapour deposition [CVD] processes characterised by the deposition of inorganic material, other than metallic material
    • C23C16/30Deposition of compounds, mixtures or solid solutions, e.g. borides, carbides, nitrides
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    • C23C16/00Chemical coating by decomposition of gaseous compounds, without leaving reaction products of surface material in the coating, i.e. chemical vapour deposition [CVD] processes
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    • C23C16/30Deposition of compounds, mixtures or solid solutions, e.g. borides, carbides, nitrides
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    • C23C16/342Boron nitride
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    • C23C16/00Chemical coating by decomposition of gaseous compounds, without leaving reaction products of surface material in the coating, i.e. chemical vapour deposition [CVD] processes
    • C23C16/22Chemical coating by decomposition of gaseous compounds, without leaving reaction products of surface material in the coating, i.e. chemical vapour deposition [CVD] processes characterised by the deposition of inorganic material, other than metallic material
    • C23C16/30Deposition of compounds, mixtures or solid solutions, e.g. borides, carbides, nitrides
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    • C23C16/00Chemical coating by decomposition of gaseous compounds, without leaving reaction products of surface material in the coating, i.e. chemical vapour deposition [CVD] processes
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    • C23C16/30Deposition of compounds, mixtures or solid solutions, e.g. borides, carbides, nitrides
    • C23C16/36Carbonitrides
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    • C23C16/00Chemical coating by decomposition of gaseous compounds, without leaving reaction products of surface material in the coating, i.e. chemical vapour deposition [CVD] processes
    • C23C16/22Chemical coating by decomposition of gaseous compounds, without leaving reaction products of surface material in the coating, i.e. chemical vapour deposition [CVD] processes characterised by the deposition of inorganic material, other than metallic material
    • C23C16/30Deposition of compounds, mixtures or solid solutions, e.g. borides, carbides, nitrides
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    • C23C16/403Oxides of aluminium, magnesium or beryllium
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    • C23C16/00Chemical coating by decomposition of gaseous compounds, without leaving reaction products of surface material in the coating, i.e. chemical vapour deposition [CVD] processes
    • C23C16/22Chemical coating by decomposition of gaseous compounds, without leaving reaction products of surface material in the coating, i.e. chemical vapour deposition [CVD] processes characterised by the deposition of inorganic material, other than metallic material
    • C23C16/30Deposition of compounds, mixtures or solid solutions, e.g. borides, carbides, nitrides
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    • C23C16/00Chemical coating by decomposition of gaseous compounds, without leaving reaction products of surface material in the coating, i.e. chemical vapour deposition [CVD] processes
    • C23C16/44Chemical coating by decomposition of gaseous compounds, without leaving reaction products of surface material in the coating, i.e. chemical vapour deposition [CVD] processes characterised by the method of coating
    • C23C16/448Chemical coating by decomposition of gaseous compounds, without leaving reaction products of surface material in the coating, i.e. chemical vapour deposition [CVD] processes characterised by the method of coating characterised by the method used for generating reactive gas streams, e.g. by evaporation or sublimation of precursor materials
    • C23C16/4488Chemical coating by decomposition of gaseous compounds, without leaving reaction products of surface material in the coating, i.e. chemical vapour deposition [CVD] processes characterised by the method of coating characterised by the method used for generating reactive gas streams, e.g. by evaporation or sublimation of precursor materials by in situ generation of reactive gas by chemical or electrochemical reaction
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    • C23COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
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    • C23C30/00Coating with metallic material characterised only by the composition of the metallic material, i.e. not characterised by the coating process
    • C23C30/005Coating with metallic material characterised only by the composition of the metallic material, i.e. not characterised by the coating process on hard metal substrates
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10STECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10S428/00Stock material or miscellaneous articles
    • Y10S428/922Static electricity metal bleed-off metallic stock
    • Y10S428/923Physical dimension
    • Y10S428/924Composite
    • Y10S428/926Thickness of individual layer specified
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
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    • Y10S428/00Stock material or miscellaneous articles
    • Y10S428/922Static electricity metal bleed-off metallic stock
    • Y10S428/9335Product by special process
    • Y10S428/938Vapor deposition or gas diffusion
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
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    • Y10TTECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00Stock material or miscellaneous articles
    • Y10T428/12All metal or with adjacent metals
    • Y10T428/12014All metal or with adjacent metals having metal particles
    • Y10T428/12028Composite; i.e., plural, adjacent, spatially distinct metal components [e.g., layers, etc.]
    • Y10T428/12049Nonmetal component
    • Y10T428/12056Entirely inorganic
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    • Y10TTECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
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    • Y10T428/12014All metal or with adjacent metals having metal particles
    • Y10T428/12028Composite; i.e., plural, adjacent, spatially distinct metal components [e.g., layers, etc.]
    • Y10T428/12063Nonparticulate metal component
    • Y10T428/12069Plural nonparticulate metal components
    • Y10T428/12076Next to each other
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
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    • Y10T428/12014All metal or with adjacent metals having metal particles
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    • Y10T428/12111Separated by nonmetal matrix or binder [e.g., welding electrode, etc.]
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    • Y10T428/26Web or sheet containing structurally defined element or component, the element or component having a specified physical dimension
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    • Y10T428/264Up to 3 mils
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  • Chemical & Material Sciences (AREA)
  • General Chemical & Material Sciences (AREA)
  • Mechanical Engineering (AREA)
  • Chemical Kinetics & Catalysis (AREA)
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  • Materials Engineering (AREA)
  • Metallurgy (AREA)
  • Organic Chemistry (AREA)
  • Inorganic Chemistry (AREA)
  • Electrochemistry (AREA)
  • Chemical Vapour Deposition (AREA)
  • Polishing Bodies And Polishing Tools (AREA)
  • Laminated Bodies (AREA)
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  • Cutting Tools, Boring Holders, And Turrets (AREA)

Abstract

A sintered hard metal body (e.g., a cutting insert) is provided as to wear resistance by depositing thereon an intermediate thin coating of a metallic carbide or metallic nitride free from binder metal and applying over this intermediate coating a thin ceramic coating free from binder metal.

Description

Изобретение относится к порошковой металлургии, в частности к ре-, жущим инструментам, выполненным из спеченных твердых сплавов.The invention relates to powder metallurgy, in particular to cutting tools made of sintered hard alloys.

Известен режущий инструмент, изготовленный из спеченного твердого сплава, содержащего карбид вольфрама и кобальт Г1]·Known cutting tool made of sintered hard alloy containing tungsten carbide and cobalt G1] ·

Наиболее близким к предлагаемому по технической сущности и достигаемому результату является режущий инструмент, содержащий подложку из спеченного твердого сплава на основе карбида вольфрама с кобальтом и поверхностный слой из карбида титана [2J.15 Недостатком известных режущих инструментов является их низкий срок службы.Closest to the proposed technical essence and the achieved result is a cutting tool containing a substrate of sintered hard alloy based on tungsten carbide with cobalt and a surface layer of titanium carbide [2J. 15 A disadvantage of the known cutting tools is their low life.

Цель изобретения - повышение срока„ службы.The purpose of the invention is to increase the service life.

Поставленная цель достигается тем, что режущий инструмент, содержащий подложку из спеченного твердого сплава на основе карбида вольфра- 2$ ма с кобальтом и слой карбида титана, дополнительно содержит наружный рлой из окиси алюминия толщиной 0,8 - 2 мкм,при атом толщина слоя карбида титана составляет 2 - 5 мкм.This goal is achieved in that the cutting tool containing a substrate of sintered tungsten carbide based on tungsten carbide- 2 $ ma with cobalt and a layer of titanium carbide additionally contains an outer core of aluminum oxide with a thickness of 0.8 - 2 microns, with an atom the thickness of the carbide layer titanium is 2 - 5 microns.

Нанесение слоев карбида титана~й окиси алюминия на спеченный твердый сплав осуществляют из газовой фазы.The application of layers of titanium carbide ~ th alumina on the sintered hard alloy is carried out from the gas phase.

Перед нанесением слоя карбида титана поверхность твердого сплава можно окислять или нитрировать. Возможно окисление слоя TiC перед нане’сением слоя окиси алюминия. Операция окисления проводится как самостоятель ная. jBefore applying a layer of titanium carbide, the surface of the hard alloy can be oxidized or nitrated. It is possible to oxidize the TiC layer before applying an alumina layer. The oxidation operation is carried out as an independent. j

Дпя повышения срока службы издения необходимо, чтобы слой карбида титана был однородным и имел хорошее сцепление с подложкой. Для обеспечения оптимальной структуры слоя карбида титана необходимо, чтобы скорость процесса осаждения была низкой.In order to increase the life of the publication, it is necessary that the titanium carbide layer be uniform and have good adhesion to the substrate. To ensure the optimal structure of the titanium carbide layer, it is necessary that the deposition process be low.

Пример 1. На подложку из спеченного твердого сплава на основе карбида вольфрама, содержащего, вес.% кобальт 9,5; карбид титана 12,0; карбид тантала 6,0; карбид ниобия ' 4,0; карбид вольфрама - остальное, при 1100°С наносят слой карбида титана из газовой фазы, содержащей,%: TiClfl 10; СНд 8; Нг82. Нанесение слоя окиси алюминия осуществляют -при той же .температуре (1100°C) из газовой фазы, содержащей, %: Н^70; 5;Example 1. On a substrate of sintered hard alloy based on tungsten carbide containing, wt.% Cobalt 9.5; titanium carbide 12.0; tantalum carbide 6.0; niobium carbide '4.0; tungsten carbide - the rest, at 1100 ° C a layer of titanium carbide is applied from the gas phase, containing,%: TiClfl 10; SND 8; N g 82. The alumina layer is applied at the same temperature (1100 ° C) from the gas phase, containing,%: Н ^ 70; 5;

СО 20; А1С13 5.СО 20; A1C1 3 5.

Испытания резания углеродистой ( стали с 1% С (твердость по Бринелю 300 кг/ммг) при скорости резания _Cutting Tests carbon (steel with 1% C (Brinell hardness of 300 kg / mm z) at a cutting speed _

160 м/мин, подаче 0,30 мм/об показы- 5 вают следующие значения срока службы + мкм160 m / min, feed 0.30 mm / rev show 5 the following values of the service life + microns

3,33.3

15,515,5

18,3 + мкм+18.3 + μm +

4,34.3

43,4 инструмента, мин Твердый сплав Твердый сплав + слой TiC, 4 '(прототип) Твердый сплав + слой Al^O-j, 4 мкм Твердый еллав + слой Al^Oj, 30 мкм Твердый сплав + слой TiC, 2 + слой АКО,, 2 мкм43.4 tools, min Hard alloy Hard alloy + TiC layer, 4 '(prototype) Hard alloy + Al ^ Oj layer, 4 μm Hard alloy + Al ^ Oj layer, 30 μm Hard alloy + TiC layer, 2 + AKO layer, 2 μm

Пример 2, На подложку из спеченного твердого сплава состава, Сб.%: кобальт 9,5; карбид титана 15,5; карбид вольфрама — -остальное, наносят сначалаExample 2, On a substrate of sintered hard alloy composition, Sat.%: cobalt 9.5; titanium carbide 15.5; tungsten carbide - the rest is applied first

TiC, затем фазы состава, приведенного 1, при 1100°С. При резаний слой слой А1^0 .>, из газовой в примере стали с твердостью, по Бринелю · 280 кг/мм^ при скорости резания 180 м/мин и подаче 0,3 мм/об установлен следующий срок службы инструмента, мин:TiC, then the phase composition shown in 1, at 1100 ° C. When cutting the layer layer A1 ^ 0.>, From gas in the example of steel with hardness, according to Brinell · 280 kg / mm ^ at a cutting speed of 180 m / min and a feed of 0.3 mm / rev, the following tool life is set, min:

Твердый сплав + слойHard alloy + layer

TiC, ,5 мкм (прототип) 14,4 Твердый сплав + слой.TiC,, 5 μm (prototype) 14.4 Carbide + layer.

TiC, 5 мкм + слойTiC, 5 μm + layer

А1^0э, 0,8 мкм 63,5 'Как следует из приведенных данных, нанесение наружного слоя из окиси алюминия толщиной 0,8-2 мкм на подложку из спеченного твердого сплава на основе карбида вольфрама со слоем карбида титана толщиной 2-5 мкм повышает срок службы режущего инструмента в 2,8-4,3 раза.A1 ^ 0 e , 0.8 μm 63.5 'As follows from the above data, the deposition of an outer layer of aluminum oxide with a thickness of 0.8-2 μm on a substrate of sintered tungsten carbide-based alloy with a layer of titanium carbide with a thickness of 2-5 microns increases the service life of the cutting tool in 2.8-4.3 times.

Claims (2)

Изобретение относитс  к порошковой металлургии, в частности к ре-. жущим инструментам, выполненным из спеченных твердых сплавов. Известен режущий инструмент, изготовленный из спеченного твердого сплава, содержащего карбид вольфрама и кобальт TI }Наиболее близким к предлагаемому по технической сущности и достигаемому результату  вл етс  режущий инструмент, содержащий подложку из спеченного твердого сплава на основ карбида вольфрама с кобальтом и поверхностный слой из карбида титана Недостатком известных режущих ин струментов  вл етс  их низкий срок службы. Цель изобретени  - повышение сро службы. Поставленна  цель достигаетс  тем, что режущий инструмент, содержащий подложку из спеченного твердо го сплава на основе карбида вольфра ма с кобальтом и слой карбида титана , дополнительно содержит наружный слой из окиси алюмини  толщиной 0,8 - 2 мкм,при атом толщина сло  к бида титана составл ет 2 -5мкм. Нанесение слоев карбида титана и окиси алюмини  на спеченный твердый сплав осуществл ют из газовой фазы. Перед нанесением сло  карбида титана поверхность твердого сплава можно окисл ть или нитрировать. Возможно окисление сло  TiC перед нанесением сло  окиси алюмини . Операци  окислени  проводитс  как самосто тельна  . ..: Дл  повышени  срока службы издени  необходимо, чтобы слой карбида титана был однородным и имел хорошее сцепление с подложкой. Дл  обеспечени  оптимальной структуры сло  карбида титана необходимо, чтобы скорость процесса осаждени  была низкой. Пример 1. На подложку из спеченного твердого сплава на основе карбида вольфрама, содержащецо, вес.%1 кобальт 9,5; карбид титана 12,0j карбид тантала 6,0; карбид ниоби  ;, 4,0; карбид вольфрама - остальное, при нанос т слой карбида титана из газовой фазы, содержащей,%: TiC 10; СНд 8; . Нанесение сло  окиси алюмини  осуществл ют При той же .температуре () из газовой фазы, содержащей, %: СО 5 СО 20; А1С15 5. Испытани  резани  углеродистой стали с 1% С (твердость по Бринел 300 кг/мм) при зкорости резани  1бО м/мин, подаче 0,30 мм/об пока вают следующие значени  срока слу инструмента, мин: Твердый сплав 3,3 Твердый сплав + + слой Tie, 4 мкм { прототип) 15,5 Твердый сплав + + слой , Твердый сплав + + слой 30 мкм Твердый сплав + + слой TiC, 2 МКМ+ + слой , 2 мкм Пример 2, На подложку из спеченного твердого сплава состава, Об.%: кобальт 9,5; кар .бид титана 15,5; карбид вольфрама . остальное, нанос т сначала слой TiC, затем - слойА1а. газово фазы состава, дтриведенного в прим 1, при . При резаний стали твердостью, по Бринелю 280 кг/мм при скорости резани  180 м/мин и подаче 0,3 мм/об установлен следу ррок службы инструменту, мин: Твердый сплав + слой TiC, .5 мкм (прототип) 14,4 Твердый сплав + слой. Tie, 5 мкм + слой , 0,8 мкм63,5 /Как следует из приведенных данных, нанесение наружного сло  из окиси алюмини  толщиной 0,8-2 мкм на подложку из спеченного твердого сплава на основе карбида вольфрама со слоем карбида титана толщиной 2-5 мкм повышает срок службы режущего инструмента в 2,8-4,3 раза. Формула изобретени  Режущий инструмент, содержащий подложку из спеченного твердого сплава на основе карбида вольфрама с кобальтом и слой из карбида титана, отличающийс  тем, что, с целью повышени  срока службы, он дополнительно содержит наружный слой из окиси алюмини  толщиной 0,8-2 мкм, при этом толщина сло  карбида титана составл ет 2-5 мкм. Источники информации, прин тые во внимание при экспертизе 1.Киффер Р., Шварцкопф п. Твергре сплавы. Металлургиздат. 1957, с. 503-505. The invention relates to powder metallurgy, in particular to re-. tools made of sintered hard alloys. A cutting tool made of sintered hard alloy containing tungsten carbide and cobalt TI is known. The closest to the proposed technical essence and the achieved result is a cutting tool containing a substrate of sintered hard alloy based on tungsten carbide with cobalt and a surface layer of titanium carbide A disadvantage of the known cutting tools is their low durability. The purpose of the invention is to increase the service life. The goal is achieved by the fact that the cutting tool, containing a substrate of sintered hard alloy based on tungsten carbide with cobalt and a layer of titanium carbide, further comprises an outer layer of aluminum oxide 0.8–2 µm thick, with an atom thickness of titanium double is 2-5 microns. The deposition of titanium carbide and alumina layers on the sintered hard alloy is carried out from the gas phase. Before applying a layer of titanium carbide, the surface of the hard alloy can be oxidized or nitrated. It is possible to oxidize the TiC layer before applying the alumina layer. The oxidation step is carried out independently. ..: In order to increase the service life of the publication, it is necessary that the titanium carbide layer be uniform and have good adhesion to the substrate. In order to ensure the optimal structure of the titanium carbide layer, it is necessary that the rate of the deposition process be low. Example 1. On a substrate of sintered hard alloy based on tungsten carbide, containing, wt.% 1 cobalt 9.5; titanium carbide 12,0j tantalum carbide 6.0; niobium carbide; 4.0; tungsten carbide - the rest, with deposited layer of titanium carbide from the gas phase, containing,%: TiC 10; SND 8; . The layer of alumina is applied at the same temperature () from the gas phase containing,%: CO 5 CO 20; A1C15 5. Cutting tests of carbon steel with 1% C (Brinell hardness 300 kg / mm) at cutting speeds of 1 bO m / min, feeding 0.30 mm / rev show the following values for tool life, min: Hard alloy 3.3 Hard alloy + + Tie layer, 4 microns {prototype) 15.5 Hard alloy + + layer, Hard alloy + + 30 micron layer Hard alloy + + TiC layer, 2 MKM + + layer, 2 microns Example 2, On a sintered substrate hard alloy composition, vol.%: cobalt 9.5; karbid titanium 15.5; Wolfram carbide . the rest is applied first with a layer of TiC, then with a layer of AA1a. the gas phase of the composition, given in ca 1, at. When steel was cut with hardness, Brinell 280 kg / mm at a cutting speed of 180 m / min and a feed of 0.3 mm / rev were installed after the service life of the tool, min: Hard alloy + TiC layer, .5 µm (prototype) 14.4 Solid alloy + layer. Tie, 5 μm + layer, 0.8 μm63.5 / As follows from the above data, the application of the outer layer of aluminum oxide with a thickness of 0.8-2 μm on a substrate of sintered hard tungsten carbide-based alloy with a layer of titanium carbide 2- thick 5 microns increases the service life of the cutting tool by 2.8-4.3 times. DETAILED DESCRIPTION OF THE INVENTION A cutting tool comprising a substrate of sintered hard tungsten carbide based on cobalt and a layer of titanium carbide, characterized in that, in order to increase the service life, it additionally contains an outer layer of alumina 0.8-2 microns thick, wherein the thickness of the titanium carbide layer is 2-5 µm. Sources of information taken into account in the examination 1.Kiffer R., Schwarzkopf P. Tvergre alloys. Metallurgizdat. 1957, p. 503-505. 2. Oberflache, 1970, 1, S. 19-20.2. Oberflache, 1970, 1, S. 19-20.
SU721848420A 1971-11-12 1972-11-10 Cutting tool SU963450A3 (en)

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