JPS63274771A - Surface-treated cemented carbide alloy member - Google Patents

Surface-treated cemented carbide alloy member

Info

Publication number
JPS63274771A
JPS63274771A JP10592587A JP10592587A JPS63274771A JP S63274771 A JPS63274771 A JP S63274771A JP 10592587 A JP10592587 A JP 10592587A JP 10592587 A JP10592587 A JP 10592587A JP S63274771 A JPS63274771 A JP S63274771A
Authority
JP
Japan
Prior art keywords
layer
cemented carbide
balance
softened
hardness
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Granted
Application number
JP10592587A
Other languages
Japanese (ja)
Other versions
JPH07122138B2 (en
Inventor
Tetsuo Komatsu
哲郎 小松
Noribumi Kikuchi
菊池 則文
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Mitsubishi Metal Corp
Original Assignee
Mitsubishi Metal Corp
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Filing date
Publication date
Application filed by Mitsubishi Metal Corp filed Critical Mitsubishi Metal Corp
Priority to JP10592587A priority Critical patent/JPH07122138B2/en
Publication of JPS63274771A publication Critical patent/JPS63274771A/en
Publication of JPH07122138B2 publication Critical patent/JPH07122138B2/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

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  • Powder Metallurgy (AREA)
  • Chemical Vapour Deposition (AREA)
  • Cutting Tools, Boring Holders, And Turrets (AREA)

Abstract

PURPOSE:To obtain a surface-treated cemented carbide alloy member free from peeling of coating layer and excellent in machinability, by successively forming an intermediate softened layer, a surface semihard layer, and a coating layer each having a specific composition on the surface of a base material for a cemented carbide alloy with a specific composition to respectively specified layer thicknesses. CONSTITUTION:A base material of cemented carbide alloy has a composition consisting of, by volume, 5-30% Co and the balance WC and further containing, if necessary, 5-30% of NaCl-type crystalline structure of the carbides (excluding WC), nitrides, and carbonitrides of the group-IVa, -Va, and -VIs metals of the periodic table. On the surface of the above, an intermediate softened layer which has a composition consisting of 15-30% Co and the balance WC and further containing, if necessary, 5-30% of the same NaCl-type crystalline structure as mentioned above is formed to 2-50mum layer thickness. On the surface of the above layer, a surface semihard layer consisting of 3-15% Co and the balance WC and further containing, if necessary, 5-30% of the same NaCl-type crystalline structure as mentioned above is formed to 0.1-30mum layer thickness. Further, a single or multiple coating layer consisting of the same carbides, etc., as mentioned above and Al2O3 is formed to 1-20mum layer thickness on the above-mentioned layer. Moreover, by constituting the above-mentioned layers of structures having respectively proper hardnesses, the surface-treated cemented carbide alloy member can be obtained.

Description

【発明の詳細な説明】 〔産業上の利用分野〕 この発明は、すぐれた耐摩耗性および耐塑性変形性を有
し、かつ靭性に富んだ、被覆層の密着性の強い、すぐれ
た切削性を示す表面被覆超硬合金部材に関するものであ
る。
[Detailed Description of the Invention] [Field of Industrial Application] The present invention has excellent wear resistance and plastic deformation resistance, is rich in toughness, has a strong adhesion of the coating layer, and has excellent machinability. The present invention relates to a surface-coated cemented carbide member showing the following.

〔従来の技術〕[Conventional technology]

従来、例えば炭化タングステン(以下weで示す)基超
硬合金基体の表面に1周期律表の4a、5a、および6
a族の金属の炭化物(但しWCを除く)、窒化物、炭窒
化物、炭酸化物、および炭酸窒化物、並びに酸化アルミ
ニウム、さらにこれらの2種以上の固溶体からなる群の
うちの1種の単層または2種以上の多重層からなる被覆
層を形成した表面被覆超硬合金部材は公知であシ、この
公知の表面被覆超硬合金部材の靭性をさらに改良するた
めに、超硬合金基体の表面[WC−Goからなる中間軟
化層、さらにその上にNaCl型結晶構造物−Coから
なる表面硬質層を設けて超硬合金基体を改質した上で最
終の被覆層を形成することにより、被覆層の密着性を改
善する方法が試みられ(特開昭55−134107号公
報)、すぐれた効果をあげている。
Conventionally, for example, 4a, 5a, and 6 of the periodic table are coated on the surface of a tungsten carbide (hereinafter referred to as we)-based cemented carbide substrate.
Group A metal carbides (excluding WC), nitrides, carbonitrides, carbonates, and carbonitrides, aluminum oxide, and solid solutions of two or more of these. A surface-coated cemented carbide member having a coating layer or a multilayer of two or more layers is known, and in order to further improve the toughness of this known surface-coated cemented carbide member, it is necessary to Surface [By modifying the cemented carbide base by providing an intermediate soft layer made of WC-Go and a hard surface layer made of NaCl-type crystal structure -Co on top of it, and then forming the final coating layer, A method of improving the adhesion of the coating layer has been attempted (Japanese Unexamined Patent Publication No. 55-134107), and has shown excellent results.

〔発明が解決しようとする問題点〕[Problem that the invention seeks to solve]

しかしながら、上記特開昭55−134107号公報記
載の方法によっても得られる被覆工具材は連続切削では
良好な特性を示すものの、断続切削では被覆層の剥離が
起るという問題点があった。
However, although the coated tool material obtained by the method described in JP-A-55-134107 exhibits good properties in continuous cutting, there is a problem in that the coating layer peels off in interrupted cutting.

〔問題点を解決するための手段〕[Means for solving problems]

そこで、本発明者等は、上記従来の表面被覆超硬合金部
材のもつ問題点を解決して、断続切削時においても耐塑
性変形性および靭性にすぐれ、かつ被覆層の密着性が高
く剥離の起らない表面被覆超硬合金部材な得べく研究を
行った結果。
Therefore, the present inventors solved the problems of the conventional surface-coated cemented carbide members, and achieved excellent plastic deformation resistance and toughness even during interrupted cutting, and high adhesion of the coating layer to prevent peeling. This is the result of research into surface-coated cemented carbide parts that prevent this from occurring.

上記超硬合金基体の表面と被覆層との間に、超硬合金基
体の内部よシも軟らかく、靭性に富んだ中間軟化層と上
記中間軟化層よシも硬質の表面準硬質層を形成すれば、
被覆層と超硬合金基体との変形に対する追従性が良好と
なシ剥離の発生が抑えられ、さらに被覆層よシのクラッ
クの伝播が抑制でき、靭性の大幅な向上がはかられ、断
続切削に対する良好な特性が得られるという知見を得た
のである。
Between the surface of the cemented carbide base and the coating layer, an intermediate softened layer is formed in which the interior of the cemented carbide base is soft and has high toughness, and a semi-hard surface layer is formed in which the interior of the cemented carbide base is also hard. Ba,
Good followability to deformation between the coating layer and the cemented carbide substrate suppresses the occurrence of peeling, further suppresses the propagation of cracks from the coating layer to the coating layer, significantly improves toughness, and facilitates interrupted cutting. They obtained the knowledge that good characteristics can be obtained for.

この発明は、かかる知見にもとづいてなされたものであ
って、 超硬合金基体の表面に形成した層厚:2〜50μmの中
間軟化層と、該中間軟化層の上に形成した層厚:0.1
〜30μmの表面準硬質層と、該表面準硬質層の上に形
成した層厚二1〜20μmの被覆層とからなる表面被覆
超硬合金部材であって、該超硬合金基体の内部を、 Co:5〜3o容量チ(以下、成分組成についてのチは
容量%)、WC:残部からなる組成、または、周期律表
の4a、5aおよび6a族の金属の炭化物(但しWCを
除く)、窒化物および炭窒化物のうち1種または2種以
上からなるNaCt型結晶構造物=5〜30%、Co:
5〜30%、we:残部からなる組成で構成し、 該中間軟化層は、 Co:15〜30%、WC:残部からなる組成、または
、周期律表の4a、5aおよび6a族の金属の炭化物(
但しWCを除く)、窒化物および炭窒化物のうち1種ま
たは2種以上からなるNaCt型結晶構造物:5〜30
%、Co: l 5〜30 %。
This invention was made based on this knowledge, and includes an intermediate softening layer with a layer thickness of 2 to 50 μm formed on the surface of a cemented carbide base, and a layer thickness of 0 μm formed on the intermediate softening layer. .1
A surface-coated cemented carbide member consisting of a semi-hard surface layer of ~30 μm and a coating layer of 21 to 20 μm in thickness formed on the semi-hard surface layer, the interior of the cemented carbide base being Co: 5 to 3o capacity CH (hereinafter, CH regarding component composition is volume %), WC: composition consisting of the remainder, or carbides of metals of groups 4a, 5a and 6a of the periodic table (excluding WC), NaCt type crystal structure consisting of one or more types of nitride and carbonitride = 5 to 30%, Co:
The intermediate softening layer has a composition consisting of Co: 15 to 30% and WC: the balance, or a composition of metals from groups 4a, 5a and 6a of the periodic table. carbide(
(excluding WC), NaCt type crystal structure consisting of one or more types of nitrides and carbonitrides: 5 to 30
%, Co: l 5-30%.

WC:残部からなる組成から構成され、該表面準硬質層
は。
WC: The surface semi-hard layer is composed of the remainder.

Co二3〜15%、WC:残部からなる組成、または2
周期律表の4a、5aおよび6a族の金属の炭化物(但
しWCを除く)、窒化物および炭窒化物のうち1種また
は2種以上からなるNaCt型結晶構造物:5〜30%
、Co:3〜15%、WC:残部からなる組成から構成
され、 該被覆層は。
Composition consisting of Co2 3-15%, WC: balance, or 2
NaCt-type crystal structure consisting of one or more types of carbides (excluding WC), nitrides, and carbonitrides of metals in groups 4a, 5a, and 6a of the periodic table: 5 to 30%
, Co: 3 to 15%, and WC: the balance.

、周期律表の4a、5aおよび6a族の金属の炭化物(
但しwCを除く)、窒化物および炭窒化物。
, carbides of metals of groups 4a, 5a and 6a of the periodic table (
(excluding wC), nitrides and carbonitrides.

炭酸化物および炭酸窒化物、並びに酸化ア”ルミニウム
、さらKこれらの2種以上の固溶体からなる群のうち1
種の単層または2種以上の多層からなる組成から構成さ
れ、 該表面率硬化層の硬さが、該中間軟化層の硬さよりもビ
ッカース硬さで5〜125%硬く、該中間軟化層は、該
超硬合金基体内部に比べて、ビッカース硬さで20〜6
0チ軟化している組織を有する表面被覆超硬合金部材に
特徴を有するものである。
One of the group consisting of solid solutions of two or more of carbonates, carbonate nitrides, aluminum oxide, and K.
The surface ratio hardened layer is 5 to 125% harder in terms of Vickers hardness than the intermediate softened layer, and the intermediate softened layer is , Vickers hardness is 20 to 6 compared to the inside of the cemented carbide base.
This is characterized by a surface-coated cemented carbide member having a zero-softened structure.

つぎに、この発明の表面被覆超硬合金部材における被覆
層、表面準硬質層、中間軟化層および超硬合金基体内部
の組成および硬さの限定理由について述べるが、上記被
覆層および超硬合金基体内部の組成は、公知のものであ
るから詳述せず、上記表面準硬質層および中間軟化層の
組成および硬さについて詳述する。
Next, the reasons for limiting the composition and hardness of the coating layer, semi-hard surface layer, intermediate softening layer, and cemented carbide base in the surface-coated cemented carbide member of the present invention will be described. Since the internal composition is well known, it will not be described in detail, but the composition and hardness of the surface semi-hard layer and the intermediate soft layer will be described in detail.

(a)表面準硬質層 被覆層の剥離は、切削時の塑性変形に対する被覆層と超
硬合金基体との靭性の不一致の程度の大きさによるとこ
ろが大きい。したがって、この発明においては、被覆層
と中間軟化層との間に、中間軟化層よりも硬い表面準硬
質層を形成し、被覆層と中間軟化層との硬さの違いを緩
和し、被覆層の強度不足を補うとともに変形に対する追
従性を改善し被覆層の密着性の向上をはかったものであ
る。
(a) Surface semi-hard layer Peeling of the coating layer largely depends on the degree of mismatch in toughness between the coating layer and the cemented carbide substrate against plastic deformation during cutting. Therefore, in this invention, a semi-hard surface layer harder than the intermediate softening layer is formed between the coating layer and the intermediate softening layer to alleviate the difference in hardness between the coating layer and the intermediate softening layer. The aim is to compensate for the lack of strength in the steel, improve the ability to follow deformation, and improve the adhesion of the coating layer.

この表面準硬質層の組成は、Co:3〜15%、WC:
残部、またはCo: 3〜15%、周期律表の4a、5
aおよび6a族の金属の炭化物(但しWCを除く)、窒
化物および炭窒化物のうち1種または2種以上からなる
NaCl型結晶構造物(以下、単にNaCl型化合物と
いう)’:5〜30%、WC:残部のいずれかから成p
、Co:3%未満では所望の靭性が得られず、15%を
越えて含有させると所望の硬さが得られず、耐摩耗性の
不足につながる。NaCL型化合物についても、5%未
満では耐摩耗性が不足し、30チを越えると靭性が不足
する。
The composition of this surface semi-hard layer is Co: 3 to 15%, WC:
The remainder, or Co: 3-15%, 4a, 5 of the periodic table
NaCl-type crystal structure (hereinafter simply referred to as NaCl-type compound) consisting of one or more types of carbides (excluding WC), nitrides, and carbonitrides of metals of group a and 6a groups (hereinafter simply referred to as NaCl-type compounds)': 5 to 30 %, WC: composed of any of the remaining parts
, Co: If the content is less than 3%, the desired toughness cannot be obtained, and if the content exceeds 15%, the desired hardness cannot be obtained, leading to insufficient wear resistance. Regarding the NaCL type compound, if it is less than 5%, the wear resistance is insufficient, and if it exceeds 30%, the toughness is insufficient.

なお、WCおよびNaCl型化合物の粒度については。Regarding the particle size of WC and NaCl type compounds.

一般に中間軟化層中のWCおよびNaCl型化合物の粒
度よりやや細い方が好ましい。
Generally, it is preferable that the particle size be slightly smaller than that of the WC and NaCl type compounds in the intermediate softening layer.

表面準硬質層の硬さは、中間軟化層の硬さよシビツカー
ス硬さで5〜125%硬いことが必要であり、5%未満
では所望の改善効果が得られず、一方125%を越えて
硬化させると、靭性低下が著しい。
The hardness of the surface semi-hard layer needs to be 5 to 125% harder in terms of hardness than the hardness of the intermediate softening layer; if it is less than 5%, the desired improvement effect cannot be obtained, while if it exceeds 125%, it is hard. When this happens, the toughness decreases significantly.

また、表面準硬質層の層厚が0.1μm未満では同様に
所望の改善効果がなく、30μmを越えると靭性の低下
をきたすという理由によシ、その層厚な0.1〜30μ
mと定めたのである。
In addition, if the thickness of the surface semi-hard layer is less than 0.1 μm, the desired improvement effect will not be obtained, and if it exceeds 30 μm, the toughness will decrease.
It was set as m.

(b)中間軟化層 表面液位超硬合金工具の欠損は、通常被覆層よりの超硬
合金基体内部へのクラック伝播により生じると考えられ
ておシ、シたがって、この発明では、上記表面準硬質層
と超硬合金基体表面部との間に、層厚:2〜50μmで
、超硬合金基体内部よシビツカース硬さで20〜60%
軟化した靭性に富んだ軟化層を形成することによって、
硬質被覆層よりのクラックの伝播を抑制すると共に、強
度および靭性の向上をはかったのである。中間軟化層の
硬さが、超硬合金基体内部に比してビッカース硬さで2
0%未満の軟化では、所望の靭性改善効果を確保するこ
とができず、一方60%を越えて軟化させると、耐塑性
変形性および被膜の耐剥離性の低下が著しいことから、
中間軟化層の硬さを基体内部硬さよりビッカース硬さで
20〜60チ軟化させた硬さとしたのである。
(b) Liquid level on the surface of the intermediate softened layer It is thought that fractures in cemented carbide tools are usually caused by crack propagation from the coating layer into the interior of the cemented carbide base. Between the semi-hard layer and the surface of the cemented carbide substrate, the layer thickness is 2 to 50 μm, and the hardness of the inside of the cemented carbide substrate is 20 to 60%.
By forming a softened layer rich in toughness,
The aim was to suppress the propagation of cracks from the hard coating layer and to improve strength and toughness. The hardness of the intermediate softened layer is 2 Vickers hardness compared to the inside of the cemented carbide base.
If the softening is less than 0%, the desired toughness improvement effect cannot be ensured, while if the softening exceeds 60%, the plastic deformation resistance and peeling resistance of the coating are significantly reduced.
The hardness of the intermediate softened layer is set to be 20 to 60 degrees softer in terms of Vickers hardness than the internal hardness of the base.

さらに、層厚が2μm未満では、同様に所望の靭性改善
効果が得られず、一方50μmを越えた層厚にすると、
著しい耐塑性変形性の低下をきたすことから、中間軟化
層の層厚を2〜50μmと定めたのである。
Furthermore, if the layer thickness is less than 2 μm, the desired toughness improvement effect cannot be obtained, whereas if the layer thickness exceeds 50 μm,
Since this results in a significant decrease in plastic deformation resistance, the thickness of the intermediate softened layer was set at 2 to 50 μm.

中間軟化層は、Co:15〜30%、WC:残部、また
は、Co:15〜30%、Na Cを型化合物:5〜3
0%、WC:残部からなる組成で構成され、その限定理
由も表面塾硬質層で述べた内容と同一である。但し、W
CおよびNaCt型化合物の粒度は。
The intermediate softening layer is composed of Co: 15-30%, WC: balance, or Co: 15-30%, Na C type compound: 5-3
0%, WC: the balance, and the reason for this limitation is the same as that described in the surface hard layer. However, W
The particle sizes of C and NaCt type compounds are.

表面準硬質層のWCおよびNaCl型化合物の粒度よシ
、やや粗い方が好ましい。
It is preferable that the particle size of the WC and NaCl type compounds in the semi-hard surface layer be slightly coarser.

なお、被覆層の層厚に関しては、その層厚が1μm未満
では所望の耐摩耗性改善効果が確保できず、一方20μ
mを越えた層厚にすると、靭性低下が著しいことから1
〜20μmと定めた。この被覆層は1通常の化学蒸着法
、イオンブレーティング法およびスパッタリング法など
の被覆層形成手段によって形成することができる。
Regarding the thickness of the coating layer, if the layer thickness is less than 1 μm, the desired effect of improving wear resistance cannot be secured;
If the layer thickness exceeds 1 m, the toughness will decrease significantly.
It was determined to be ~20 μm. This coating layer can be formed by conventional coating layer forming methods such as chemical vapor deposition, ion blasting, and sputtering.

〔実施例〕〔Example〕

つぎに、この発明を実施例にもとづいて具体的に説明す
る。
Next, the present invention will be specifically explained based on examples.

超硬合金基体の内部組成として、第1表に示すような最
終成分組成となるように市販の原料粉末を配合し、ボー
ルミルにて48時時間式混合し。
Commercially available raw material powders were blended so as to have the final component composition shown in Table 1 as the internal composition of the cemented carbide base, and mixed for 48 hours in a ball mill.

乾燥し、プレスすることによって圧粉体を成形し。Form a green compact by drying and pressing.

ついで、圧粉体の表面に、別途予め用意した第1表の中
間軟化層形成のための所定の配合粉末混合スラリーをN
2ガス雰囲気中で一様に噴霧して減圧下で乾燥し、引き
続いて表面準硬質層形成のための第1表に示した配合粉
混合スラリーを同様に所定の厚みになるようN2ガス雰
囲気中で一様に噴霧し、減圧下で乾燥し、ついで温度:
1400℃に1時間保持して焼結することによって、表
面準硬質層および中間軟化層を有するSNU 432型
スローアウエイチツプを製造し、表面準硬質層および中
間軟化層の層厚およびビッカース硬さを測定し、第1表
に示した。
Next, N
After uniformly spraying in a N2 gas atmosphere and drying under reduced pressure, the mixed powder mixture slurry shown in Table 1 for forming a semi-hard layer on the surface was similarly sprayed to a predetermined thickness in a N2 gas atmosphere. Spray uniformly at , dry under reduced pressure and then at temperature:
By holding and sintering at 1400°C for 1 hour, a SNU 432 type indexable chip with a semi-hard surface layer and an intermediate softening layer was manufactured, and the layer thickness and Vickers hardness of the semi-hard surface layer and the intermediate softening layer were determined. The results are shown in Table 1.

上記SNU 432型スローアウエイチツプの表面に、
0.0513+のプレホーニングを施し、化学蒸着用処
理炉内に装入し、大気圧下でTiCL4 : 4 % 
tCH4:4%およびN2二92%(容量%)からなる
ガスを導入しながら、温度:1050℃に5時間保持す
ることによって1層厚:5μmのTiCffflを被覆
し、つづいてAlCl3: 2%、Co□:6チおよび
N2:9296(容量%)からなるガスを導入しながら
、温度: 1000℃で2時間保持することによって層
厚:1μmの’yt2o3層を被覆し、計6μmの被覆
層を形成し、本発明スローアウエイチップを製造した。
On the surface of the above SNU 432 type throwaway tip,
It was prehoned to 0.0513+, charged into a chemical vapor processing furnace, and heated to 4% TiCL4 under atmospheric pressure.
While introducing a gas consisting of 4% tCH4 and 92% (volume %) N2, the temperature was kept at 1050°C for 5 hours to coat TiCfffl with a thickness of 5 μm, followed by 2% AlCl3, While introducing a gas consisting of Co□:6 and N2:9296 (volume %), a temperature of 1000°C was maintained for 2 hours to coat a 'yt2o3 layer with a layer thickness of 1 μm, resulting in a total coating layer of 6 μm. A throw-away tip of the present invention was manufactured.

上記本発明スローアウェイチップについて、(1)被削
材: SN0M439 (HB: 320)切削速度:
 150 m/mJL 送り: 0.6 NL/ rev。
Regarding the above indexable insert of the present invention, (1) Work material: SN0M439 (HB: 320) Cutting speed:
150 m/mJL Feed: 0.6 NL/rev.

切込み:3B の条件で連続切削試験を行ない、逃げ面摩耗およびクレ
ータ摩耗を測定した。
Continuous cutting tests were conducted under conditions of depth of cut: 3B, and flank wear and crater wear were measured.

(2)被削材: SN0M439(HB:270)溝付
き丸棒 切削速度:120m/醜 送シ:0,4顛/ rev。
(2) Work material: SN0M439 (HB: 270) Grooved round bar Cutting speed: 120m/Ugly feed: 0.4 pieces/rev.

切込み23M の条件で断続切削試験を行ない、切刃が欠損するまでの
時間を測定した。
An interrupted cutting test was conducted at a depth of cut of 23M, and the time until the cutting edge broke was measured.

上記(1)および〔2)の切削試験の結果についても第
1表に示した。
The results of the cutting tests in (1) and [2) above are also shown in Table 1.

ついで、従来例として、上記特開昭55−134107
号公報に示された、WCを含有しない表面硬化層を有す
る従来のスローアウェイチップを用いて、上記(1)お
よび(2)の条件と同一の条件で切削試験をした。その
結果も第2表に示した。
Next, as a conventional example, the above-mentioned Japanese Patent Application Laid-Open No. 55-134107
A cutting test was conducted under the same conditions as (1) and (2) above using the conventional throw-away tip shown in the above publication and having a hardened surface layer that does not contain WC. The results are also shown in Table 2.

〔発明の効果〕〔Effect of the invention〕

上記本発明スローアウェイチップを用いて切削試験をし
た結果(第1表)と従来のスローアウェイチップを用い
て切削試験をした結果(第2表)とを対比してみると、
連続切削試験においては両者ともほぼ同じ効果を奏する
が、断続切削試験に対しては、本発明スローアウェイチ
ップの方がはるかにすぐれていることが明らかである。
Comparing the results of cutting tests using the indexable insert of the present invention (Table 1) and the results of cutting tests using the conventional indexable insert (Table 2),
Although both have almost the same effect in continuous cutting tests, it is clear that the indexable insert of the present invention is far superior to interrupted cutting tests.

したがって、この発明を切削工具として用いて%表面に
凹凸があるような被切削材を切削しても、従来の切削工
具よシ欠損時間が長く、断続切削に対してすぐれた効果
を奏するものである。
Therefore, even if the present invention is used as a cutting tool to cut a workpiece that has an uneven surface, the chipping time is longer than that of conventional cutting tools, and it is effective against interrupted cutting. be.

Claims (1)

【特許請求の範囲】 超硬合金基体の表面に形成した層厚:2〜50μmの中
間軟化層と、該中間軟化層の上に形成した層厚:0.1
〜30μmの表面準硬質層と、該表面準硬質層の上に形
成した層厚:1〜20μmの被覆層とからなる表面被覆
超硬合金部材であつて、該超硬合金基体の内部を、 Co:5〜30%、WC:残部からなる組成、または、 周期律表の4a、5aおよび6a族の金属の炭化物(但
しWCを除く)、窒化物および炭窒化物のうち1種また
は2種以上からなるNaCl型結晶構造物:5〜30%
、Co:5〜30%、WC:残部からなる組成から構成
し、 該中間軟化層は、 Co:15〜30%、WC:残部からなる組成または、 周期律表の4a、5aおよび6a族の金属の炭化物(但
しWCを除く)、窒化物および炭窒化物のうち1種また
は2種以上からなるNaCl型結晶構造物:5〜30%
、Co:15〜30%、WC:残部からなる組成から構
成され、 該表面準硬質層は、 Co:3〜15%、WC:残部からなる組成または、 周期律表の4a、5aおよび6a族の金属の炭化物(但
しWCを除く)、窒化物および炭窒化物のうち1種また
は2種以上からなるNaCl型結晶構造物:5〜30%
、Co:3〜15%、WC:残部からなる組成から構成
され、 該被覆層は、 周期律表の4a、5aおよび6a族の金属の炭化物(但
しWCを除く)、窒化物および炭窒化物、炭酸化物およ
び炭酸窒化物、並びに酸化アルミニウム、さらにこれら
の2種以上の固溶体からなる群のうちの1種の単層また
は2種以上の多層からなる組成から構成され(以上、%
は容量%)、該表面準硬化層の硬さが、該中間軟化層の
硬さよりもビッカース硬さで5〜125%硬く、該中間
軟化層は、該超硬合金基体内部に比べて、ビッカース硬
さで20〜60%軟化している組織を有することを特徴
とする表面被覆超硬合金部材。
[Claims] An intermediate softened layer formed on the surface of the cemented carbide substrate with a layer thickness of 2 to 50 μm, and a layer thickness formed on the intermediate softened layer of 0.1 μm.
A surface coated cemented carbide member consisting of a semi-hard surface layer of ~30 μm and a coating layer formed on the semi-hard surface layer with a thickness of 1 to 20 μm, the interior of the cemented carbide base being A composition consisting of Co: 5 to 30%, WC: the balance, or one or two of carbides (excluding WC), nitrides, and carbonitrides of metals in groups 4a, 5a, and 6a of the periodic table. NaCl type crystal structure consisting of the above: 5 to 30%
, Co: 5-30%, WC: balance, the intermediate softening layer has a composition consisting of Co: 15-30%, WC: balance, or a composition of groups 4a, 5a and 6a of the periodic table. NaCl-type crystal structure consisting of one or more of metal carbides (excluding WC), nitrides, and carbonitrides: 5 to 30%
, Co: 15-30%, WC: balance, the surface semi-hard layer has a composition consisting of Co: 3-15%, WC: balance, or Groups 4a, 5a and 6a of the periodic table. NaCl-type crystal structure consisting of one or more of metal carbides (excluding WC), nitrides, and carbonitrides: 5 to 30%
, Co: 3 to 15%, and WC: the balance, and the coating layer includes carbides (excluding WC), nitrides, and carbonitrides of metals in groups 4a, 5a, and 6a of the periodic table. , carbonate, carbonate nitride, aluminum oxide, and a composition consisting of a single layer or a multilayer of two or more of the solid solutions of two or more of these (%
is % by volume), the hardness of the semi-hardened surface layer is 5 to 125% harder in Vickers hardness than the hardness of the intermediate softened layer, and the intermediate softened layer has a Vickers hardness of 5 to 125% harder than the hardness of the intermediate softened layer, and A surface-coated cemented carbide member characterized by having a structure whose hardness is softened by 20 to 60%.
JP10592587A 1987-04-28 1987-04-28 Surface coated cemented carbide member Expired - Lifetime JPH07122138B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP10592587A JPH07122138B2 (en) 1987-04-28 1987-04-28 Surface coated cemented carbide member

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP10592587A JPH07122138B2 (en) 1987-04-28 1987-04-28 Surface coated cemented carbide member

Publications (2)

Publication Number Publication Date
JPS63274771A true JPS63274771A (en) 1988-11-11
JPH07122138B2 JPH07122138B2 (en) 1995-12-25

Family

ID=14420435

Family Applications (1)

Application Number Title Priority Date Filing Date
JP10592587A Expired - Lifetime JPH07122138B2 (en) 1987-04-28 1987-04-28 Surface coated cemented carbide member

Country Status (1)

Country Link
JP (1) JPH07122138B2 (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5204167A (en) * 1989-02-23 1993-04-20 Toshiba Tungaloy Co., Ltd. Diamond-coated sintered body excellent in adhesion and process for preparing the same
JP2000218408A (en) * 1999-01-29 2000-08-08 Kyocera Corp Coated cemented carbide cutting tool
JP2019065330A (en) * 2017-09-29 2019-04-25 三菱マテリアル株式会社 Composite sintered body

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5204167A (en) * 1989-02-23 1993-04-20 Toshiba Tungaloy Co., Ltd. Diamond-coated sintered body excellent in adhesion and process for preparing the same
JP2000218408A (en) * 1999-01-29 2000-08-08 Kyocera Corp Coated cemented carbide cutting tool
JP2019065330A (en) * 2017-09-29 2019-04-25 三菱マテリアル株式会社 Composite sintered body

Also Published As

Publication number Publication date
JPH07122138B2 (en) 1995-12-25

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