JP2828511B2 - Surface coated TiCN based cermet - Google Patents

Surface coated TiCN based cermet

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Publication number
JP2828511B2
JP2828511B2 JP2416054A JP41605490A JP2828511B2 JP 2828511 B2 JP2828511 B2 JP 2828511B2 JP 2416054 A JP2416054 A JP 2416054A JP 41605490 A JP41605490 A JP 41605490A JP 2828511 B2 JP2828511 B2 JP 2828511B2
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JP
Japan
Prior art keywords
cermet
weight
film
hard
ticn
Prior art date
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Expired - Fee Related
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JP2416054A
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Japanese (ja)
Other versions
JPH04231468A (en
Inventor
裕久 小西
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Kyocera Corp
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Kyocera Corp
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Description

【発明の詳細な説明】DETAILED DESCRIPTION OF THE INVENTION

【0001】[0001]

【産業上の利用分野】本発明は、耐摩耗性、靱性に優
れ、切刃部における下地の硬度が高く、特に鋳鉄用切削
工具として有用で且つ被削材の加工面の平滑性に優れた
表面被覆TiCN基サーメットに関する。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention is excellent in abrasion resistance and toughness, and has a high hardness of a base material at a cutting edge, and is particularly useful as a cutting tool for cast iron and has excellent smoothness of a machined surface of a work material. The present invention relates to a surface-coated TiCN-based cermet.

【0002】[0002]

【従来技術】従来から、切削用焼結体としてはWC−C
oを主成分とする超硬合金が主として用いられていた
が、最近ではTiの炭化物、窒化物、炭窒化物を主成分
とするサーメット焼結体が用いられている。
2. Description of the Related Art Conventionally, WC-C has been used as a cutting sintered body.
A cemented carbide mainly containing o is mainly used, but recently, a cermet sintered body mainly containing carbides, nitrides, and carbonitrides of Ti has been used.

【0003】このようなサーメット系焼結体としてはT
iCを主成分とし、鉄族金属を結合相とし、さらに周期
律表第4a、5a、6a族金属の炭化物、窒化物、炭窒
化物を硬質相成分として加えたTiC基サーメットが主
流であった。しかし乍らこのようなTiC基サーメット
焼結体では耐熱性、強靱性に劣ることから、上記組成に
さらにTiN等の窒化物、炭窒化物を含有させることが
提案された。これは、TiN自体が靱性に富むことによ
り、焼結体に靱性を付与するとともに、熱伝導率が高い
ことにより、耐熱衝撃性、耐熱塑性変形性を向上させよ
うとするものである。
As such a cermet-based sintered body, T
The mainstream was a TiC-based cermet containing iC as a main component, an iron group metal as a binder phase, and carbides, nitrides, and carbonitrides of metals of groups 4a, 5a and 6a of the periodic table as hard phase components. . However, since such a TiC-based cermet sintered body is inferior in heat resistance and toughness, it has been proposed to further include a nitride such as TiN or a carbonitride in the above composition. This is intended to impart toughness to the sintered body due to the high toughness of TiN itself, and to improve thermal shock resistance and thermal plastic deformation due to high thermal conductivity.

【0004】そこで、従来よりTiNを含有するTiC
基サーメットに対し、さらに各種の改良がなされてい
る。例えば特公昭59−14534号では、液晶出現温
度以下で窒素を炉内に導入し、焼結体表面に靱性に富む
軟化層を形成させることが、また、特公昭59−171
76号ではCo還元雰囲気で焼成することにより、特定
の硬度を有する硬質層を形成させることが、さらに、特
公昭60−34618号によれば焼成後の降温時にCo
雰囲気と成すことにより表面内部とも均一な特性を有す
るサーメットを得ることが提案されている。
Accordingly, TiC containing TiN has been conventionally used.
Various improvements have been made to the base cermet. For example, Japanese Patent Publication No. Sho 59-14534 discloses that nitrogen is introduced into a furnace at a temperature lower than the liquid crystal appearance temperature to form a softened layer having a high toughness on the surface of a sintered body.
No. 76, it is possible to form a hard layer having a specific hardness by firing in a Co reducing atmosphere. Further, according to Japanese Patent Publication No. 60-34618, when the temperature is lowered after firing,
It has been proposed to obtain a cermet having uniform characteristics inside the surface by forming an atmosphere.

【0005】[0005]

【発明が解決しようとする問題点】しかし乍ら、鋳鉄用
切削工具として高速切削加工時の耐摩耗性の知見から
は、特公昭59−14534号および特公昭60−34
618号の記載の切削工具では表面硬度が低いために、
性能上不十分である。一方、特公昭59−17176号
には表面に硬質層を形成させる方法が開示されているも
ののその表面硬度はせいぜいビッカース硬度(Hv)で
1800までしか達成されておらず、それ以上の硬度を
有する硬質層を形成させる際には、硬質形成成分中にM
2 CおよびWCを多量に含有させなければ達成されな
いが、このようにMo、C、WCを多量に含む組成では
実質上、切削工具としての他の特性を劣化させる結果と
なってまう。
However, from the knowledge of wear resistance during high-speed cutting as a cutting tool for cast iron, JP-B-59-14534 and JP-B-60-34 are disclosed.
The cutting tool described in No. 618 has a low surface hardness,
Insufficient in performance. On the other hand, Japanese Patent Publication No. 59-17176 discloses a method of forming a hard layer on the surface, but the surface hardness is at most only Vickers hardness (Hv) up to 1800, and has a higher hardness. When forming the hard layer, M is contained in the hard forming component.
This cannot be achieved unless a large amount of o 2 C and WC is contained, but such a composition containing a large amount of Mo, C, and WC results in substantially deteriorating other properties as a cutting tool.

【0006】そこで、本出願人は、先にTiCN基サー
メットの作成時に、焼成中の雰囲気を高窒素ガス雰囲気
より急激に真空に戻すことにより、その表面部にビッカ
ース硬度が2000以上の高硬度の層を形成させること
により、鋳鉄用切削工具として優れた耐摩耗性耐欠損性
を有するサーメットが得られることを提案した。
[0006] Therefore, the applicant of the present invention, when preparing the TiCN-based cermet, first returned the atmosphere during firing to a vacuum more rapidly than the high nitrogen gas atmosphere, so that the surface portion of the cermet had a Vickers hardness of 2000 or more. It was proposed that by forming a layer, a cermet having excellent wear resistance and fracture resistance as a cutting tool for cast iron could be obtained.

【0007】しかしながら、かかるTiCN基サーメッ
トは、その表面部分のTiの含有比率が非常に少なくな
り、表面部にW量が多くなることに起因して、特に鉄系
材料を被削材として切削加工する場合に、W等と被削材
とが反応し、被削材の切削加工後の表面に荒れが生じる
という問題があることがわかった。
However, such a TiCN-based cermet has a very low Ti content ratio on its surface and a large amount of W on its surface. In such a case, it has been found that there is a problem in that W and the like react with the work material, and the surface of the work material after cutting is roughened.

【0008】[0008]

【問題点を解決するための手段】本発明者は上記問題点
に対し研究を重ねた結果、先に提案した表面部にビッカ
ース硬度2000以上の高硬度を有するTiCN基サー
メットの表面に、該サーメットの表面部のTi量より富
むTi含有硬質膜を形成することにより、該サーメット
の有する優れた特性を維持しつつ、被削材との反応性を
顕著に低減できるとともにさらに優れた切削特性が得ら
れることを見出した。
Means for Solving the Problems As a result of repeated studies on the above problems, the present inventors have found that the surface of a TiCN-based cermet having a high Vickers hardness of 2000 or more on the surface of the cermet is proposed. By forming a Ti-containing hard film that is richer than the amount of Ti in the surface portion of the cermet, the reactivity with the work material can be significantly reduced while maintaining the excellent characteristics of the cermet, and further excellent cutting characteristics can be obtained. Was found to be.

【0009】即ち、本発明の表面被覆TiCN基サーメ
ットは、Tiの炭化物、窒化物、あるいは炭窒化物を5
0乃至80重量%、周期律表第6a族元素の炭化物を1
0乃至40重量%の割合で含有するとともに、(窒素/
炭素+窒素)で表される原子比が0.4乃至0.6の範
囲にある硬質相成分60乃至95重量%と、鉄族金属を
主成分とする結合相成分5乃至40重量%とから成ると
ともに、表面から50μmの間にビッカース硬度200
0kg/mm2 以上の部分が存在するTiCN基サーメ
ットの表面に、該TiCN基サーメットよりも多くのT
iを含有し、平均粒径0.4μm以下、鉄族金属の含有
量が100ppm以下のTi含有硬質膜を被覆してなる
ことを特徴とするものである。
That is, the surface-coated TiCN-based cermet according to the present invention comprises Ti carbide, nitride or carbonitride of 5%.
0 to 80% by weight, 1% of a carbide of Group 6a element of the periodic table
0 to 40% by weight.
60 to 95% by weight of a hard phase component having an atomic ratio represented by (carbon + nitrogen) in a range of 0.4 to 0.6, and 5 to 40% by weight of a binder phase component mainly composed of an iron group metal. And a Vickers hardness of 200 between 50 μm from the surface
On the surface of the TiCN-based cermet where a portion of 0 kg / mm 2 or more exists, more T than the TiCN-based cermet.
It is characterized by being coated with a Ti-containing hard film containing i and having an average particle size of 0.4 μm or less and an iron group metal content of 100 ppm or less.

【0010】本発明において、母材として用いられるT
iCN基サーメットは、硬質相成分として、Tiの炭化
物、窒化物あるいは炭窒化物を50乃至80重量%、特
に55乃至65重量%と、W、Mo等の周期律表第6a
族元素の炭化物を10乃至40重量%、特に15乃至3
0重量%の割合で含有する。
[0010] In the present invention, T
The iCN-based cermet contains 50 to 80% by weight, particularly 55 to 65% by weight of a carbide, nitride or carbonitride of Ti as a hard phase component, and a periodic table 6a such as W or Mo.
10 to 40% by weight, especially 15 to 3%
It is contained at a ratio of 0% by weight.

【0011】このような硬質相成分において、Tiの量
が50重量%を下回ると耐摩耗性が低下し、80重量%
を越えると焼結性が低下し好ましくない。また、第6a
族元素は粒成長抑制、結合相とのぬれ性を向上させる効
果を有するが、10重量%を下回ると上記効果が得られ
ず、硬質相が粗大化し、硬度、強度が低下する。また4
0重量%を越えるとη相等の不健全相が生じると共に焼
結が困難となる。
In such a hard phase component, if the amount of Ti is less than 50% by weight, the abrasion resistance is reduced, and
If it exceeds sinterability, the sinterability is undesirably reduced. In addition, the 6a
Group elements have the effect of suppressing grain growth and improving the wettability with the binder phase. However, if the content is less than 10% by weight, the above effects cannot be obtained, the hard phase becomes coarse, and the hardness and strength decrease. Also 4
If it exceeds 0% by weight, an unhealthy phase such as an η phase is generated and sintering becomes difficult.

【0012】また、硬質相成分としては上記の他、耐ク
レータ摩耗性向上を目的としてTa、Nb、さらに耐塑
性変形向上を目的としてZr、V、Hf等の窒化物、炭
化物、炭窒化物を合量で0.1乃至40重量%の割合で
含むことも可能であるが、40重量%を超えると耐摩耗
性劣化、ポア、ボイドの発生が著しく増加する傾向にあ
り好ましくない。
In addition to the above, other hard phase components include Ta and Nb for the purpose of improving crater wear resistance, and nitrides, carbides and carbonitrides such as Zr, V and Hf for the purpose of improving plastic deformation resistance. Although it is possible to contain it in a ratio of 0.1 to 40% by weight in total, it is not preferable that the content exceeds 40% by weight because deterioration of abrasion resistance, generation of pores and voids tend to remarkably increase.

【0013】一方、結合相はFe、Co、Ni等の鉄族
金属を主体として成るもので、一部、硬質相形成成分が
含まれる場合がある。
On the other hand, the binder phase is mainly composed of an iron group metal such as Fe, Co, and Ni, and may partially include a hard phase forming component.

【0014】焼結体全体として硬質相成分は60乃至9
5重量%、結合相成分は5乃至40重量%の割合から成
る。
The hard phase component is 60 to 9 as a whole of the sintered body.
5% by weight, the binder phase component comprising 5 to 40% by weight.

【0015】本発明における組成上の特徴は、硬質相成
分中において(窒素/炭素+窒素)で表される原子比が
0.4乃至0.6、特に0.4乃至0.5の範囲に設定
される点にある。即ち、この原子比が0.4を下回ると
靱性、耐摩耗性の向上が望めず、本発明の目的が達成さ
れず、0.6を越えると焼結体中にポア、ボイドが発生
し工具としての信頼性が低下する。
The feature of the composition in the present invention is that the atomic ratio represented by (nitrogen / carbon + nitrogen) in the hard phase component is in the range of 0.4 to 0.6, particularly 0.4 to 0.5. The point that is set. That is, if this atomic ratio is less than 0.4, improvement in toughness and wear resistance cannot be expected, and the object of the present invention is not achieved. If it exceeds 0.6, pores and voids are generated in the sintered body, and As the reliability decreases.

【0016】さらに、本発明におけるサーメットは、図
1に示すように表面から50μmまでの表層部にビッカ
ース硬度が2000以上の高硬度な部分が存在するもの
である。かかる表層部の高硬度な部分は、後述する製法
からも、表面部の結合相が現象するとともに表層部の第
6a族元素量が増加することによる。このような硬質部
が存在することによって被覆サーメット用母材の耐塑性
変形性を大きく向上させることができる。
Further, as shown in FIG. 1, the cermet according to the present invention has a high hardness portion having a Vickers hardness of 2000 or more in a surface layer portion up to 50 μm from the surface. Such a high hardness portion of the surface layer portion is due to the fact that the bonding phase on the surface portion occurs and the amount of the Group 6a element in the surface layer portion increases, also from the manufacturing method described later. The presence of such a hard portion can greatly improve the plastic deformation resistance of the coated cermet base material.

【0017】通常、表面に高硬度部が存在する場合、靱
性低下により、チッピング、欠損等が発生し易くなる
が、本発明によれば、前述した特定の組成、特に窒素を
多量に含むことによって靱性が付与され、チッピング、
欠損等の発生のない優れた母材となる。
In general, when a high hardness portion is present on the surface, chipping, chipping and the like are likely to occur due to a decrease in toughness. However, according to the present invention, the above-mentioned specific composition, particularly containing a large amount of nitrogen, Toughness is imparted, chipping,
It is an excellent base material with no defects or the like.

【0018】本発明おけるTiCN基サーメットは、上
記構成により、窒素を多量に含むことによる靱性、耐摩
耗性の向上効果を長期に旦り維持することができ、しか
も表面に高硬度な部分が存在することから、表面被覆鋳
鉄切削工具用母材としての長寿命化、高信頼性を図るこ
とが可能性となる。
The TiCN-based cermet according to the present invention can maintain the effect of improving toughness and abrasion resistance by containing a large amount of nitrogen for a long period of time with the above structure, and has a high hardness portion on the surface. Therefore, it becomes possible to achieve a long life and high reliability as a base material for a surface-coated cast iron cutting tool.

【0019】上述したサーメットによれば、表層部にお
けるTi量が低いことに起因して、例えば構造用合金鋼
SCM435を被削材として切削を行うと、サーメット
中の鉄族金属や硬質相中のW等が被削材と反応し、仕上
げ面が荒れる場合がある。よって本発明によれば、かか
るTiCN基サーメットの表面にTiを含有する硬質膜
を被覆する。
According to the above-described cermet, when the cutting is performed using, for example, the structural alloy steel SCM435 as a work material due to the low Ti content in the surface layer, the iron group metal in the cermet or the hard phase in the hard phase is cut. W reacts with the work material and the finished surface may be roughened. Therefore, according to the present invention, the surface of the TiCN-based cermet is coated with a hard film containing Ti.

【0020】この硬質膜は、サーメット母材と被削材と
の反応性を抑制させるために、硬質膜のTi量が母材の
Ti量、特に表層部のTi量よりも多い膜とすることに
より前述したサーメットの被削材との反応性を抑制する
ことができる。また、サーメット表面に硬質膜を形成す
る際に、サーメット表面に富む鉄族金属が硬質膜中に拡
散し、これが硬質膜の硬度、被削材との低反応性等の被
膜本来の特性を劣化させてしまう。よって、この硬質膜
は、その膜中に含有される鉄族金属量を100ppm以
下、特に70ppm以下に制御することが必要である。
In order to suppress the reactivity between the cermet base material and the work material, the hard film should be a film in which the amount of Ti in the hard film is larger than the amount of Ti in the base material, particularly the amount of Ti in the surface layer. Thereby, the reactivity of the cermet with the work material can be suppressed. In addition, when forming a hard film on the cermet surface, the iron-group metal rich in the cermet surface diffuses into the hard film, which deteriorates the hardness of the hard film and the original properties of the film such as low reactivity with the work material. Let me do it. Therefore, in this hard film, it is necessary to control the amount of iron group metal contained in the film to 100 ppm or less, particularly 70 ppm or less.

【0021】さらに、硬質膜を構成する結晶の粒径は、
膜の硬度、強度を左右する要因となり、その結晶粒径が
小さいほど硬質且つ高強度、高靱性な被膜となる。よっ
て本発明によれば、この硬質膜の結晶粒径を0.4μm
以下、特に0.3μm 以下に制御することにより硬質膜
としての本来の機能を発揮するとともに、膜中破壊に起
因する粒脱落、しいては膜剥離を防止することができ
る。
Further, the grain size of the crystal constituting the hard film is:
This is a factor that affects the hardness and strength of the film. The smaller the crystal grain size, the harder the film, the higher the strength and the higher the toughness. Therefore, according to the present invention, the crystal grain size of this hard film is 0.4 μm
By controlling the thickness to 0.3 μm or less, the original function as a hard film can be exhibited, and at the same time, it is possible to prevent the falling off of the particles due to the breakage in the film and the peeling of the film.

【0022】なお、Ti量がサーメット母材中のTi量
よりも多いTi含有硬質膜としては、TiC、TiN、
TiCN等が好適であり、これらの膜中には場合により
酸素が含まれることもある。
Incidentally, as the Ti-containing hard film in which the amount of Ti is larger than the amount of Ti in the cermet base material, TiC, TiN,
TiCN and the like are preferable, and oxygen may be contained in these films in some cases.

【0023】この硬質膜は、サーメット表面に1〜10
μm の厚みで被覆するのが望ましく、膜厚が1μm より
小さいと、被削材との反応性抑制効果が小さく、被削材
の表面に荒れが生じ、10μm より厚いと母材と被覆層
との熱膨張差により使用時に剥離し易くなる。
This hard film has a thickness of 1 to 10 on the surface of the cermet.
It is desirable to coat with a thickness of μm. If the thickness is less than 1 μm, the effect of suppressing the reactivity with the work material is small, and the surface of the work material is roughened. Is easy to peel off during use due to the thermal expansion difference.

【0024】本発明の表面被覆TiCN基サーメットの
製造方法によれば、まず母材を製造するに際して組成と
して、Tiの炭化物、窒化物、あるいは炭窒化物を50
乃至80重量%、周期律表第6a族元素の炭化物を10
乃至40重量%の割合で含有するとともに、(窒素/炭
素+窒素)で表される原子比が0.4乃至0.6の範囲
にある硬質相成分60乃至95重量%と、結合相成分5
乃至40重量%とから成る成形体を作製する。
According to the method for producing a surface-coated TiCN-based cermet according to the present invention, first, when producing a base material, a composition of Ti carbide, nitride or carbonitride of 50% is used.
From 80% by weight to 10% of carbides of Group 6a elements of the periodic table.
A hard phase component having an atomic ratio of (nitrogen / carbon + nitrogen) in the range of 0.4 to 0.6 and a binder phase component of 5 to 40% by weight.
To 40% by weight.

【0025】具体的には原料粉末としてTiC、Ti
N、TiCN等を、また第6a族系としてはWC、Mo
2 C、MoC等を、あるいはこれらの複合炭化物、複合
炭窒化物を用い、上記の組成となるように調合した後、
公知の成形手段、例えばプレス成形、押出し成形、鋳込
み成形、射出成形、冷間静水圧成形等で成形する。
Specifically, TiC, Ti
N, TiCN, etc., and WC, Mo
After using 2 C, MoC, etc., or their composite carbides and composite carbonitrides to prepare the above composition,
Molding is performed by known molding means, for example, press molding, extrusion molding, casting molding, injection molding, cold isostatic molding, or the like.

【0026】この時、前述したようにTa、Nb、Z
r、V、Hf等の炭化物、窒化物、炭窒化物を組合わせ
て用いることも当然可能である。なお、Ti系としては
TiCを用いると焼結性が低下し、部分的粒成長を起こ
す場合がるため、Ti(CN)あるいはTiNとの組合
せがより好ましい。
At this time, as described above, Ta, Nb, Z
Naturally, it is also possible to use a combination of carbides, nitrides, and carbonitrides such as r, V, and Hf. When TiC is used as the Ti-based material, sinterability is reduced, and partial grain growth may occur. Therefore, a combination with Ti (CN) or TiN is more preferable.

【0027】次に、上記成形体を焼成する。焼成は、1
400〜1700℃の焼成温度で行われるが、本発明に
よれば、サーメット表面部分に高硬度の部分を形成させ
るために、まず、0.5Torr以下の真空炉内で加熱
し、所定の時間に70Torr以上、とくに100〜2
00Torrの圧力の窒素ガスを導入する。
Next, the compact is fired. Firing is 1
According to the present invention, in order to form a high hardness portion on the cermet surface portion, first, the material is heated in a vacuum furnace of 0.5 Torr or less, and is heated for a predetermined time. 70 Torr or more, especially 100-2
Nitrogen gas at a pressure of 00 Torr is introduced.

【0028】この窒素ガスの導入は、昇温過程におい
て、鉄族金属の液相出現温度以上で導入する。即ち、液
相出現温度以上で窒素ガスを導入することにより、成形
体中に含まれるTiN等の窒化物の熱分解による窒素ガ
スの発生を抑制し、結果的に焼結体中にポア、ボイドが
残留するのを防止することができる。しかし、窒素ガス
の導入の時期が焼結最高温度到達後では、窒化物の分解
抑制効果は得られず、焼結体表面に荒れが生じる。
This nitrogen gas is introduced at a temperature higher than the liquid phase appearance temperature of the iron group metal in the heating process. That is, by introducing nitrogen gas at a temperature higher than the liquid phase appearance temperature, generation of nitrogen gas due to thermal decomposition of nitrides such as TiN contained in the compact is suppressed, and as a result, pores and voids are introduced into the sintered compact. Can be prevented from remaining. However, when the introduction time of the nitrogen gas reaches the maximum sintering temperature, the effect of suppressing the decomposition of the nitride is not obtained, and the surface of the sintered body is roughened.

【0029】窒素ガスは、炉内の温度が最高焼結温度に
達した後は、所定時間保持後、ただちに真空に戻して焼
成を続ける。これは、最高焼結温度到達後にさらに圧力
を上げると、焼結体表面部に脆い窒化層が生成され、焼
肌面の荒れを生じるとともに、表面部の靱性を著しく低
下させてしまう。
After the temperature in the furnace reaches the maximum sintering temperature, the nitrogen gas is maintained for a predetermined time and then immediately returned to a vacuum to continue firing. If the pressure is further increased after reaching the maximum sintering temperature, a brittle nitride layer is formed on the surface of the sintered body, causing the surface of the burnt surface to be roughened and significantly reducing the toughness of the surface.

【0030】なお、導入させる窒素ガス圧力は、窒化物
の熱分解を十分に抑制し得る圧力であることが必要であ
るが、この窒素ガス圧力は焼結体表面部に形成される改
善層の硬度に大きく影響する。これは、窒素ガス導入
後、成形体内部と炉内雰囲気との間に圧力を生じてい
る。そこへ、急激に真空に戻すと表面付近は内部に対
し、結合相量が減少することにより、硬度が高くなる。
また、組織上、表面付近の結晶が球状化することおよび
第6a族元素が多量に含まれることにより靱性が向上す
るものと考えられる。なお、ビッカース硬度2000以
上の硬質部を形成させるためには窒素ガス圧力を70T
orr以上に設定することが必要である。
The pressure of the nitrogen gas to be introduced needs to be a pressure capable of sufficiently suppressing the thermal decomposition of the nitride, and the pressure of the nitrogen gas is set to a value for the improvement layer formed on the surface of the sintered body. It greatly affects hardness. This causes a pressure between the inside of the compact and the atmosphere in the furnace after the introduction of nitrogen gas. If the pressure is rapidly returned to vacuum, the hardness increases due to a decrease in the amount of the binder phase in the vicinity of the surface relative to the inside.
Further, it is considered that the toughness is improved by making the crystal near the surface spherical in the structure and by containing a large amount of the Group 6a element. In order to form a hard portion having a Vickers hardness of 2000 or more, the nitrogen gas pressure is set to 70T.
It is necessary to set it to orr or more.

【0031】このようにして作製したサーメットを母材
とし、特に切削工加工時の被削材仕上面品位を向上させ
る目的により、被削材との反応性の低いTi化合物を主
体とする被膜を形成する、実質的にはサーメット表層付
傍のTi含有量よりもさらに高いTi化合物被膜を形成
する。また、この被膜は鉄族金属は100ppm以下と
実質的に含まず、さらに被膜強度の維持より、被膜の平
均粒径は0.4μm以下とする必要がある。具体的に
は、熱CVD、プラズマCVD、レーザCVD等の化学
気相成長法(CVD法)、スパッタリング、イオンプレ
ーティング等の物理的蒸着法(PDV法)、あるいは気
相含浸法等が採用されるが、本発明に基づき硬質膜の粒
径を0.4μm 以下に制御するにはイオンプレーティン
グ、プラズマCVD法、スパッタリングが望ましい。
The cermet prepared as described above is used as a base material, and a coating mainly composed of a Ti compound having low reactivity with the work material is used for the purpose of improving the surface finish of the work material particularly during cutting. A Ti compound film is formed, which is substantially higher than the Ti content near the cermet surface layer. In addition, this coating contains substantially no iron group metal of 100 ppm or less, and the average particle size of the coating needs to be 0.4 μm or less in order to maintain the strength of the coating. Specifically, a chemical vapor deposition method (CVD method) such as thermal CVD, plasma CVD, or laser CVD, a physical vapor deposition method (PDV method) such as sputtering or ion plating, or a gas phase impregnation method is used. However, in order to control the particle size of the hard film to 0.4 μm or less based on the present invention, ion plating, plasma CVD, and sputtering are preferable.

【0032】また、鉄族金属の硬質膜中への混入量を1
00ppm以下に制限するとともに膜付着強度を考慮し
た場合、イオンプレーティング、プラズマCVD法が等
が望ましく、特にイオンプレーティング法によれば、成
膜温度が低いことに起因して膜の結晶粒の成長速度が小
さく、しかも母材からの鉄族金属の拡散が抑制されるた
めに膜中への混入を防止することができる。また、成膜
にあたっては、反応炉内の設備等において鉄族金属製の
部品を極力排除するように考慮することも必要である。
Further, the amount of the iron group metal mixed into the hard film is 1
When the concentration is limited to not more than 00 ppm and the film adhesion strength is taken into consideration, ion plating, plasma CVD and the like are desirable. In particular, according to the ion plating method, the crystal grain size of the film is low due to the low film formation temperature. Since the growth rate is low and the diffusion of the iron group metal from the base material is suppressed, the incorporation into the film can be prevented. Further, in film formation, it is necessary to consider that parts made of iron group metal should be eliminated as much as possible in facilities and the like in the reaction furnace.

【0033】[0033]

【実施例】原料粉末として平均粒径が1〜1.5μm の
Ti(CN)、TiN、TiC、WC、Mo2 C、Nb
C、NbN、VC、Ni、Coを用い、表1の組成に調
合後、振動ミルで粉砕を行い、バインダーを添加したも
のをTNGA332チップ用の形状にプレス成形し、3
00℃で脱バインダー後、表1の仕様で焼成を行った。
なお、表1における焼成条件において窒素ガスは導入
後、焼結最高温度には5分後保持し、ただちに真空に戻
した。
EXAMPLES As raw material powder, Ti (CN), TiN, TiC, WC, Mo 2 C, Nb having an average particle size of 1 to 1.5 μm
Using C, NbN, VC, Ni, and Co, the mixture was blended into the composition shown in Table 1, and then pulverized with a vibration mill. The binder-added product was press-formed into a shape for a TNGA332 chip.
After removing the binder at 00 ° C., firing was performed according to the specifications shown in Table 1.
After the nitrogen gas was introduced under the firing conditions in Table 1, the maximum sintering temperature was maintained after 5 minutes, and the vacuum was immediately returned.

【0034】得られた焼結体に対し、硬質相の炭素、窒
素を定量分析し、(N/C+N)原子比を求めた。な
お、各試料について試料を約5°の角度で研磨し、該研
磨面に対し垂直方向でビッカース硬度を表面からの距離
(深さ)を変えて測定し、その硬度分布を見た。
The obtained sintered body was quantitatively analyzed for carbon and nitrogen in the hard phase to determine the (N / C + N) atomic ratio. Each sample was polished at an angle of about 5 °, the Vickers hardness was measured in a direction perpendicular to the polished surface while changing the distance (depth) from the surface, and the hardness distribution was observed.

【0035】硬質膜は、イオンプレーティング法により
母材温度を300〜700℃に設定して3μm の膜厚に
なるようにTiN、TiCN、TiCNO膜を形成し
た。また、被膜における結晶の平均粒径をSEMによ
り、膜中の鉄族金属の含有量をICP分析により測定し
た。
As the hard film, a TiN, TiCN, TiCNO film was formed by ion plating at a base material temperature of 300 to 700 ° C. so as to have a thickness of 3 μm. The average grain size of the crystals in the film was measured by SEM, and the content of iron group metal in the film was measured by ICP analysis.

【0036】また、各試料に対し、下記の条件で耐摩耗
性試験を行い、フランク摩耗量(mm)を測定し、また
欠損性試験により非欠損コーナー数を調べた。結果は表
2に示した。
Each sample was subjected to an abrasion resistance test under the following conditions, the flank wear amount (mm) was measured, and the number of non-deleted corners was examined by a defect test. The results are shown in Table 2.

【0037】(摩耗試験条件) 被削材 SCM435 切削速度 250m/min 切り込み 2mm 送り 0.3mm/rev 切削時間 10min(Abrasion test conditions) Work material SCM435 Cutting speed 250 m / min Cutting depth 2 mm Feeding 0.3 mm / rev Cutting time 10 min

【0038】(欠損性試験) 被削材 SCM435(4ツ溝入り) 切削速度 100m/min 切り込み 2mm 送り 0.3mm/rev 切削時間 1min(Fracture test) Work material SCM435 (with 4 grooves) Cutting speed 100 m / min Cutting depth 2 mm Feeding 0.3 mm / rev Cutting time 1 min

【0039】また、仕上面の評価として表面粗さ計を用
いて、被削材仕上げ面状態をRmaxにて表現する手法
にて行い、この値が10s以上のものを×、10s未満
のものを○として評価した。
The evaluation of the finished surface is performed by a method of expressing the finished surface state of the work material by Rmax using a surface roughness meter. If the value is 10 s or more, x is less than 10 s. O was evaluated.

【0040】[0040]

【表1】 [Table 1]

【0041】[0041]

【表2】 [Table 2]

【0042】なお、表1中、試料番号1、2、6(比較
例)についてはその表面から0.2mmまでの硬度分布
を図1に示した。
In Table 1, for samples Nos. 1, 2, and 6 (Comparative Examples), the hardness distribution from the surface to 0.2 mm is shown in FIG.

【0043】表1の結果から明らかなように、(N/C
+N)比が0.4を下回るサーメットを母材として用い
た試料番号7は焼結体表面に粗れが生じており、耐摩耗
性も悪い。逆に比が0.6を越える試料番号11では良
好な焼結体を得られず、耐摩耗テストができなかった。
また導入するN2 圧が低く、ビッカース硬度2000以
上の硬質層が形成されていないサーメットの表面に硬質
膜を形成した試料番号6は、切削途中にて著しい異常摩
耗を生じて切削不能となった。
As is clear from the results in Table 1, (N / C
Sample No. 7 using a cermet having a (+ N) ratio of less than 0.4 as a base material has a rough surface on the sintered body and has poor wear resistance. Conversely, in sample No. 11 having a ratio exceeding 0.6, a good sintered body could not be obtained, and a wear resistance test could not be performed.
Sample No. 6, in which the N 2 pressure to be introduced was low and a hard film was formed on the surface of a cermet in which a hard layer having a Vickers hardness of 2,000 or more was not formed, was markedly abnormally worn in the middle of cutting, and could not be cut. .

【0044】これに対して本発明品に基づき、表面部に
2000以上のビッカース硬度を有する部分が形成され
たサーメットの表面に微細組織からなるTi含有硬質膜
を形成した本発明品はいずれも優れた耐摩耗性と耐欠損
性を示すとともに被削材の表面状態も非常に良好なもの
であった。
On the other hand, based on the product of the present invention, the product of the present invention in which a Ti-containing hard film composed of a microstructure is formed on the surface of a cermet having a portion having a Vickers hardness of 2000 or more on the surface portion is excellent. The surface condition of the work material was very good while exhibiting wear resistance and chipping resistance.

【0045】[0045]

【発明の効果】以上詳述した通り、本発明の表面被覆T
iCN基サーメットは、表面の耐摩耗性に極めて優れた
ものであり、特に鋳鉄用の切削工具として優れた切削特
性を示し、且つ被削材の切削加工後の表面の平滑性に優
れ、工具としての長寿命化を達成することができる。
As described in detail above, the surface coating T of the present invention
iCN-based cermets are extremely excellent in wear resistance of the surface, exhibit excellent cutting characteristics especially as cutting tools for cast iron, and have excellent surface smoothness after cutting of the work material. Life can be extended.

【図面の簡単な説明】[Brief description of the drawings]

【図1】サーメット母材の表面から、0.2mmまでの
硬度分布を示す図であり、図中、No,1、2は本発明
品、No,6は比較品を示す。
FIG. 1 is a diagram showing a hardness distribution from the surface of a cermet base material to 0.2 mm from the surface of the cermet base material.

Claims (1)

(57)【特許請求の範囲】(57) [Claims] 【請求項1】Tiの炭化物、窒化物、あるいは炭窒化物
を50乃至80重量%、周期律表第6a族元素の炭化物
を10乃至40重量%の割合で含有するとともに、(窒
素/炭素+窒素)で表される原子比が0.4乃至0.6
の範囲にある硬質相成分60乃至95重量%と、鉄族金
属を主成分とする結合相成分5乃至40重量%とから成
るとともに、表面から50μmの間にビッカース硬度2
000kg/mm2 以上の部分が存在するTiCN基サ
ーメットの表面に、該TiCN基サーメットよりも多く
のTiを含有し、平均粒径0.4μm以下、鉄族金属の
含有量が100ppm以下のTi含有硬質膜を被覆して
なることを特徴とする表面被覆TiCN基サーメット。
1. A titanium carbide, nitride or carbonitride of 50 to 80% by weight and a carbide of a Group 6a element of the periodic table in a ratio of 10 to 40% by weight, and (Nitrogen / carbon + The atomic ratio represented by nitrogen) is 0.4 to 0.6
And a binder phase component mainly composed of an iron group metal in an amount of 60 to 95% by weight, and a Vickers hardness of 2 to 50 μm from the surface.
The surface of the TiCN-based cermet where a portion of 000 kg / mm 2 or more is present contains more Ti than the TiCN-based cermet, the average particle diameter is 0.4 μm or less, and the content of iron group metal is 100 ppm or less. A surface-coated TiCN-based cermet characterized by being coated with a hard film.
JP2416054A 1990-12-27 1990-12-27 Surface coated TiCN based cermet Expired - Fee Related JP2828511B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP2416054A JP2828511B2 (en) 1990-12-27 1990-12-27 Surface coated TiCN based cermet

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP2416054A JP2828511B2 (en) 1990-12-27 1990-12-27 Surface coated TiCN based cermet

Publications (2)

Publication Number Publication Date
JPH04231468A JPH04231468A (en) 1992-08-20
JP2828511B2 true JP2828511B2 (en) 1998-11-25

Family

ID=18524307

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Country Status (1)

Country Link
JP (1) JP2828511B2 (en)

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* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP5004145B2 (en) * 2004-06-09 2012-08-22 株式会社タンガロイ Cermet and coated cermet and methods for producing them
JP5729777B2 (en) 2010-09-07 2015-06-03 住友電工ハードメタル株式会社 Surface coated cutting tool
JP5062541B2 (en) * 2011-03-15 2012-10-31 住友電工ハードメタル株式会社 Cutting edge replacement type cutting tool
CN109972014A (en) * 2017-12-28 2019-07-05 厦门钨业股份有限公司 A kind of TiCN based ceramic metal

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* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH0768623B2 (en) * 1985-10-25 1995-07-26 日立ツール株式会社 Surface coated cemented carbide
JPS6458402A (en) * 1987-08-25 1989-03-06 Dijet Ind Co Ltd Coated tip for cutting work
JPH01129971A (en) * 1987-11-13 1989-05-23 Sumitomo Electric Ind Ltd Manufacture of coated cutting tool
JP2769821B2 (en) * 1988-03-11 1998-06-25 京セラ株式会社 TiCN-based cermet and method for producing the same

Also Published As

Publication number Publication date
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