JP3317124B2 - Cermet cutting tool with excellent fracture resistance and method of manufacturing the same - Google Patents

Cermet cutting tool with excellent fracture resistance and method of manufacturing the same

Info

Publication number
JP3317124B2
JP3317124B2 JP01882996A JP1882996A JP3317124B2 JP 3317124 B2 JP3317124 B2 JP 3317124B2 JP 01882996 A JP01882996 A JP 01882996A JP 1882996 A JP1882996 A JP 1882996A JP 3317124 B2 JP3317124 B2 JP 3317124B2
Authority
JP
Japan
Prior art keywords
torr
cutting tool
concentration
powder
range
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.)
Expired - Lifetime
Application number
JP01882996A
Other languages
Japanese (ja)
Other versions
JPH09207005A (en
Inventor
隆史 藤澤
清弘 照内
勝尚 野中
清一郎 中村
久史 辻崎
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 Materials Corp
Original Assignee
Mitsubishi Materials Corp
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Mitsubishi Materials Corp filed Critical Mitsubishi Materials Corp
Priority to JP01882996A priority Critical patent/JP3317124B2/en
Publication of JPH09207005A publication Critical patent/JPH09207005A/en
Application granted granted Critical
Publication of JP3317124B2 publication Critical patent/JP3317124B2/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Description

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

【0001】[0001]

【発明の属する技術分野】この発明は、耐欠損性に優れ
た少なくとも逃げ面に焼き肌面を有するサーメット製切
削工具およびその製造方法に関するものである。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a cermet cutting tool excellent in fracture resistance and having at least a flank surface on a flank, and a method for producing the same.

【0002】[0002]

【従来の技術】近年、CoおよびNiの内の1種または
2種を主成分とする結合相:5〜25重量%を含有し、
残りがTiの炭窒化物を主成分とし、さらにTiおよび
Wの複炭窒化物を含む硬質分散相からなるTiCN基サ
ーメット製切削工具が用いられていることは広く知られ
ている。
2. Description of the Related Art Recently, a binder phase containing one or two of Co and Ni as main components: 5 to 25% by weight,
It is widely known that a cutting tool made of a TiCN-based cermet is used, the remainder being mainly composed of a carbonitride of Ti and a hard dispersed phase containing a double carbonitride of Ti and W.

【0003】これらTiCN基サーメット製切削工具
は、特開平4−2173号公報に示されている真空雰囲
気で焼結する方法または特開平2−93036号公報に
示されている液相温度以上で窒素ガスを導入し、指定温
度到達後再び真空に戻して焼結する方法により製造され
る。
[0003] These cutting tools made of TiCN-based cermet can be sintered by a method of sintering in a vacuum atmosphere disclosed in Japanese Patent Application Laid-Open No. 4-2173 or a liquid nitrogen temperature above the liquid phase temperature disclosed in Japanese Patent Application Laid-Open No. 2-93036. It is manufactured by a method in which a gas is introduced, and after reaching a specified temperature, the vacuum is returned again and sintering is performed.

【0004】また、これら従来法でTiCN基サーメッ
ト製切削工具を製造すると、焼結中に脱窒現象が起きる
と同時に表面近傍と内部の間でTi、Wなどの移動が起
こり、その結果、表面近傍は内部に比べてTiおよびN
が不足し、Wが富化するために、表面でTiおよびNの
含有量は最小となり、Wの含有量は最大となることも知
られている。
When a cutting tool made of a TiCN-based cermet is manufactured by these conventional methods, a denitrification phenomenon occurs during sintering, and at the same time, movement of Ti, W, etc. between the vicinity of the surface and the inside thereof occurs. The vicinity is Ti and N compared to the inside.
It is also known that the content of Ti and N on the surface is minimized and the content of W is maximized due to lack of carbon and enrichment of W.

【0005】[0005]

【発明が解決しようとする課題】この従来の表面でNお
よびTiの含有量が最小でかつWの含有量が最大である
焼き肌面を有するTiCN基サーメット製切削工具を用
いて鉄系材料を切削すると、鉄との親和性が低いNおよ
びTiの含有量が少なくかつ鉄との親和性が高いWの含
有量が多い焼き肌面は切削中に被削材との間に溶着現象
を起こし、この現象は特に切削工具の逃げ面に起きやす
い。切削時に切削工具の刃先に被削材との溶着現象が起
きると、溶着物は生成脱落を繰り返し、脱落時に溶着物
とともに工具の一部も共に脱落するいわゆる溶着チッピ
ングによる欠損を起こし、このため従来のTiCN基サ
ーメット製切削工具では耐欠損性が不足していた。
SUMMARY OF THE INVENTION An iron-based material is cut using a TiCN-based cermet cutting tool having a burnt surface with the minimum N and Ti contents and the highest W content on the conventional surface. When cutting, the burnt surface with a low content of N and Ti, which have low affinity for iron, and a high content of W, which has high affinity for iron, causes a welding phenomenon with the work material during cutting. This phenomenon is particularly likely to occur on the flank of the cutting tool. If a welding phenomenon occurs with the work material at the cutting edge of the cutting tool during cutting, the welded material repeatedly forms and falls off. With the cutting tool made of TiCN-based cermet, the fracture resistance was insufficient.

【0006】[0006]

【課題を解決するための手段】そこで、本発明者らは、
従来よりも耐欠損性に優れたTiCN基サーメット製切
削工具を得るべく研究を行った結果、N、TiおよびW
の濃度勾配の生成は焼結時の所定温度保持中の真空雰囲
気下で起こるので、まず、焼結炉内を10-1Torr以
下の真空に保持しながら加熱し、1200〜1350℃
の範囲内の所定温度に加熱された時点で1〜60Tor
rの窒素ガスを導入し、さらに加熱して1400〜15
50℃の範囲内の所定温度到達後ただちに焼結炉内を1
-1Torr以下の真空に戻し、引き続いて焼結炉内を
10-1Torr以下の真空雰囲気に保持しながら140
0〜1550℃の範囲内の所定温度に保持した後、再び
1〜20Torrの窒素ガスを導入すると、表面近傍と
内部の間でN、Ti、Wなどの移動および再移動が起こ
り、その結果、表面近傍は内部に比べてNおよびTiが
富化し、Wが不足するために、表面近傍でNおよびTi
の含有量は極小値をとり、Wの含有量は極大値をとるよ
うな濃度勾配となって、耐欠損性に優れたサーメット製
切削工具が得られる、という研究結果が得られたのであ
る。
Means for Solving the Problems Accordingly, the present inventors have:
As a result of studying to obtain a TiCN-based cermet cutting tool having higher fracture resistance than conventional, N, Ti and W
Is generated in a vacuum atmosphere while maintaining a predetermined temperature at the time of sintering. First, the inside of the sintering furnace is heated while being kept at a vacuum of 10 -1 Torr or less, at 1200 to 1350 ° C.
1 to 60 Torr when heated to a predetermined temperature within the range
r nitrogen gas is introduced and further heated to 1400-15
Immediately after reaching the predetermined temperature in the range of 50 ° C,
The pressure is returned to a vacuum of 0 -1 Torr or less, and subsequently, the pressure in the sintering furnace is maintained at a vacuum atmosphere of 10 -1 Torr or less.
After maintaining at a predetermined temperature within the range of 0 to 1550 ° C., when nitrogen gas of 1 to 20 Torr is introduced again, movement and re-movement of N, Ti, W, etc. occur between the vicinity of the surface and the inside, and as a result, N and Ti are enriched in the vicinity of the surface compared to the inside and W is insufficient.
Has a minimum value, and the content of W has a concentration gradient such that it has a maximum value, thereby obtaining a cermet cutting tool having excellent fracture resistance.

【0007】この発明は、かかる研究結果に基づいてな
されたものであって、 (1) CoおよびNiの内の1種または2種を主成分
とする結合相:5〜25重量%を含有し、残りがTiの
炭化物、窒化物および炭窒化物、並びにTiおよびWの
複炭窒化物を含む硬質分散相からなり、少なくとも逃げ
面に焼き肌面を有するサーメット製切削工具において、
前記焼き肌面の表面から内部に向かって組成分析を行っ
たときの窒素濃度分布の極小値が表面より1〜100μ
mの範囲内にあり、かつ焼き肌面の表面の窒素濃度が極
小値の1.1〜5.0倍の範囲にあり、前記焼き肌面の
表面から内部に向かって組成分析を行ったときのTi濃
度分布の極小値が表面より1〜100μmの範囲内にあ
り、かつ焼き肌面の表面のTi濃度が極小値の1.2〜
1.5倍の範囲にあり、前記焼き肌面の表面から内部に
向かって組成分析を行ったときのW濃度分布の極大値が
表面より1〜100μmの範囲内にあり、かつ焼き肌面
の表面のW濃度が極大値の0.5〜0.9倍の範囲にあ
る耐欠損性に優れたサーメット製切削工具、 (2) Co粉末およびNi粉末の内の1種または2
種:5〜25重量%を配合し、残りがTiの炭化物、窒
化物および炭窒化物粉末の内の1種または2種、WC粉
末、並びにMo、V、Nb、Ta、Zr、Crの炭化物
粉末の内の1種または2種以上を配合し、混合して得ら
れた混合粉末をプレス成形して成形体を作製し、この成
形体を焼結炉に装入し、焼結するサーメット製切削工具
の製造方法において、前記焼結は、焼結炉内を10-1
orr以下の真空に保持しながら加熱し、1200〜1
350℃の範囲内の所定温度に加熱された時点で1〜6
0Torrの窒素ガスを導入し、さらに加熱して140
0〜1550℃の範囲内の所定温度到達後ただちに焼結
炉内を10-1Torr以下の真空に戻し、引き続いて焼
結炉内を10-1Torr以下の真空雰囲気に保持しなが
ら1400〜1550℃の範囲内の所定温度に保持した
後、再び1〜20Torrの窒素ガスを導入して保持
し、ついで冷却開始と同時に焼結炉内雰囲気をを10-1
Torr以下の真空に戻すサーメット製切削工具の製造
方法、に特徴を有するものである。
The present invention has been made on the basis of the above research results, and (1) a binder phase containing one or two of Co and Ni as a main component: containing 5 to 25% by weight. A cermet cutting tool comprising a hard dispersed phase containing carbides, nitrides and carbonitrides of Ti, and double carbonitrides of Ti and W, and having at least a flank surface on a flank;
The minimum value of the nitrogen concentration distribution when performing composition analysis from the surface of the baked skin surface to the inside is 1 to 100 μm from the surface.
m, and the nitrogen concentration on the surface of the baked surface is in the range of 1.1 to 5.0 times the minimum value, and the composition analysis is performed from the surface of the baked surface to the inside. The minimum value of the Ti concentration distribution is within a range of 1 to 100 μm from the surface, and the Ti concentration on the surface of the baked surface is the minimum value of 1.2 to
1.5 times, the maximum value of the W concentration distribution when the composition analysis is performed from the surface to the inside of the burnt surface is within a range of 1 to 100 μm from the surface, and the burnt surface is A cermet-made cutting tool excellent in fracture resistance having a surface W concentration in the range of 0.5 to 0.9 times the maximum value; (2) one or two of Co powder and Ni powder
Species: 5 to 25% by weight is blended, and the balance is one or two of carbides, nitrides and carbonitride powders of Ti, WC powders, and carbides of Mo, V, Nb, Ta, Zr, and Cr. One or two or more of the powders are blended, and the mixed powder obtained by mixing is press-molded to produce a compact, and the compact is placed in a sintering furnace and sintered to produce a cermet. In the method for manufacturing a cutting tool, the sintering is performed in a sintering furnace at 10 -1 T.
heating while maintaining the vacuum at or
When heated to a predetermined temperature within the range of 350 ° C., 1 to 6
0 Torr of nitrogen gas was introduced and further heated to 140
Immediately after reaching a predetermined temperature within the range of 0 to 1550 ° C., the inside of the sintering furnace is returned to a vacuum of 10 −1 Torr or less, and subsequently, the inside of the sintering furnace is maintained at a vacuum atmosphere of 10 −1 Torr or less, 1400 to 1550. after holding at a predetermined temperature in the range of ° C., again held by introduction of nitrogen gas 1~20Torr, then cooled at the same time as the start of the sintering furnace atmosphere 10 -1
A method for manufacturing a cermet cutting tool that returns to a vacuum of Torr or less.

【0008】この発明のサーメット製切削工具と従来の
サーメット製切削工具との差を一層理解しやすくするた
めに、この発明のサーメット製切削工具の代表的な焼き
肌面の表層部のN濃度、Ti濃度、W濃度およびこれら
の濃度分布と従来のサーメット製切削工具の代表的な焼
き肌面の表層部のN濃度、Ti濃度、W濃度およびこれ
らの濃度分布を図1に示した。図1からこの発明のサー
メット製切削工具の代表的な焼き肌面の表層部のN濃
度、Ti濃度、W濃度およびこれらの濃度分布には極小
値および極大値があるが、従来のサーメット製切削工具
の代表的な焼き肌面の表層部のN濃度、Ti濃度、W濃
度およびこれらの濃度分布には極小値および極大値がな
く、この点でこの発明のサーメット製切削工具と従来の
サーメット製切削工具とは大きく異なることが分かる。
In order to make it easier to understand the difference between the cermet cutting tool of the present invention and the conventional cermet cutting tool, the typical N concentration of the surface layer of the burnt surface of the cermet cutting tool of the present invention is as follows. FIG. 1 shows the Ti concentration, the W concentration, the distribution of these concentrations, and the N concentration, the Ti concentration, the W concentration, and the distribution of these concentrations in the surface layer of a typical burnt surface of a conventional cermet cutting tool. From FIG. 1, there is a minimum value and a maximum value in the N concentration, the Ti concentration, the W concentration, and the concentration distribution of the surface layer portion of the typical burnt surface of the cermet cutting tool of the present invention. There is no minimum value or maximum value in the N concentration, Ti concentration, W concentration and these concentration distributions of the surface layer portion of the typical burnt surface of the tool. In this respect, the cermet cutting tool of the present invention and the conventional cermet It turns out that it is greatly different from a cutting tool.

【0009】次に、この発明のサーメット製切削工具の
結合相、焼き肌面の表面のN濃度、Ti濃度、W濃度お
よびこれらの濃度分布、並びにこの発明のサーメット製
切削工具の製造条件における限定理由を説明する。 A、サーメット製切削工具の限定理由 (a) 結合相 CoおよびNiのうち1種または2種を主成分とした焼
き肌面の結合相は、その含有量が5重量%未満では耐欠
損性が不足し、一方、25重量%を越えると耐摩耗性が
不足するところから5〜25重量%に定めた。
Next, the binding phase of the cermet cutting tool of the present invention, the N concentration, the Ti concentration, the W concentration of the surface of the burnt surface and the concentration distribution thereof, and the limitations on the manufacturing conditions of the cermet cutting tool of the present invention. Explain why. A, Reasons for limiting cermet cutting tools (a) Binder phase The binder phase of the baked surface mainly containing one or two of Co and Ni has a fracture resistance when its content is less than 5% by weight. In contrast, if it exceeds 25% by weight, the wear resistance is insufficient.

【0010】(b) N濃度 この発明のサーメット製切削工具において、焼き肌面の
表面から内部に向かって組成分析を行ったときのN濃度
分布の極小値が表面より1〜100μmの範囲内にあ
り、かつ表面でのN濃度が極小値の1.1〜5.0倍の
範囲にあることが好ましい。N濃度分布の極小値が表面
より1μm未満の所にあると溶着現象が改善されず、一
方、100μmを越えた深部にあると表面の硬度が不足
し、所望の耐摩耗性が得られないからである。N濃度分
布の極小値は表面より10〜50μmの範囲内にあり、
かつ表面でのN濃度は極小値の1.5〜3倍の範囲にあ
ることが一層好ましい。
(B) N Concentration In the cermet cutting tool of the present invention, the minimum value of the N concentration distribution when the composition analysis is performed from the surface of the burnt surface to the inside thereof is within a range of 1 to 100 μm from the surface. It is preferable that the N concentration on the surface is 1.1 to 5.0 times the minimum value. If the minimum value of the N concentration distribution is less than 1 μm from the surface, the welding phenomenon is not improved, while if it is deeper than 100 μm, the hardness of the surface is insufficient and the desired wear resistance cannot be obtained. It is. The minimum value of the N concentration distribution is within a range of 10 to 50 μm from the surface,
Further, the N concentration at the surface is more preferably in the range of 1.5 to 3 times the minimum value.

【0011】(c) Ti濃度 この発明のサーメット製切削工具において、焼き肌面の
表面から内部に向かって組成分析を行ったときのTi濃
度分布の極小値が表面より1〜100μmの範囲内にあ
り、かつ表面でのTi濃度が極小値の1.1〜2.0倍
の範囲にあることが好ましい。Ti濃度分布の極小値が
表面より1μm未満にあるようでは溶着現象が改善され
ず、一方、100μmを越えた深部に在ると表面の硬度
が不足し、所望の耐摩耗性が得られないからである。T
i濃度分布の極小値は表面より10〜50μmの範囲内
にあり、かつ表面でのTi濃度は極小値の1.2〜1.
5倍の範囲にあることが一層好ましい。
(C) Ti Concentration In the cermet cutting tool of the present invention, the minimum value of the Ti concentration distribution when the composition analysis is performed from the surface of the burnt surface to the inside thereof is within a range of 1 to 100 μm from the surface. In addition, it is preferable that the Ti concentration on the surface is in the range of 1.1 to 2.0 times the minimum value. If the minimum value of the Ti concentration distribution is less than 1 μm from the surface, the welding phenomenon is not improved, while if it is deeper than 100 μm, the hardness of the surface is insufficient and the desired wear resistance cannot be obtained. It is. T
The minimum value of the i concentration distribution is within the range of 10 to 50 μm from the surface, and the Ti concentration on the surface is the minimum value of 1.2 to 1.
More preferably, it is in the range of 5 times.

【0012】(d) W濃度 この発明のサーメット製切削工具において、焼き肌面の
表面から内部に向かって組成分析を行ったときのW濃度
分布の極大値が表面より1〜100μmの範囲内にあ
り、かつ表面でのW濃度が極大値の0.5〜0.9倍の
範囲にあることが好ましい。W濃度分布の極大値が表面
より1μm未満にあると溶着現象が改善されず、一方、
100μmを越えた深部に在ると表面の硬度が不足し、
所望の耐摩耗性が得られないからである。W濃度分布の
極大値は表面より10〜50μmの範囲内にあり、かつ
表面でのW濃度は極大値の0.6〜0.8倍の範囲にあ
ることが一層好ましい。
(D) W concentration In the cermet cutting tool of the present invention, the maximum value of the W concentration distribution when the composition is analyzed from the surface of the burnt surface to the inside thereof is within a range of 1 to 100 μm from the surface. In addition, it is preferable that the W concentration on the surface is in the range of 0.5 to 0.9 times the maximum value. When the maximum value of the W concentration distribution is less than 1 μm from the surface, the welding phenomenon is not improved.
If it is deeper than 100 μm, the surface hardness will be insufficient,
This is because desired abrasion resistance cannot be obtained. More preferably, the maximum value of the W concentration distribution is in the range of 10 to 50 μm from the surface, and the W concentration on the surface is in the range of 0.6 to 0.8 times the maximum value.

【0013】 B、サーメット製切削工具の製造方法の限定理由 この発明のサーメット製切削工具の製造方法は、Co粉
末およびNi粉末の内の1種または2種:5〜25重量
%を配合し、残りがTiの炭化物、窒化物および炭窒化
物粉末の内の1種または2種、WC粉末、並びにMo、
V、Nb、Ta、Zr、Crの炭化物粉末の内の1種ま
たは2種以上を配合し、混合して得られた混合粉末をプ
レス成形して成形体を作製し、この成形体を焼結炉に装
入し、焼結するもので、この発明のサーメット製切削工
具の製造方法は成形体製造までは従来の方法と同一であ
るが成形体を焼結するための焼結条件が従来法と相違
し、その相違点の限定理由を以下に説明する。
B, Reasons for Limiting the Method of Manufacturing a Cermet Cutting Tool The method of manufacturing a cermet cutting tool of the present invention is characterized in that one or two of Co powder and Ni powder: 5 to 25% by weight are blended. The balance is one or two of carbide, nitride and carbonitride powders of Ti, WC powder, and Mo,
One or two or more of carbide powders of V, Nb, Ta, Zr, and Cr are blended, and a mixed powder obtained by mixing is press-molded to produce a compact, and this compact is sintered. The method for manufacturing a cermet cutting tool of the present invention is the same as the conventional method until the compact is manufactured, but the sintering conditions for sintering the compact are the conventional methods. The reason for limiting the difference is described below.

【0014】(e) 真空度 焼結時の昇温時は焼結炉内を10-1Torr以下の真空
に保持しながら加熱する理由は、焼結炉内の真空度が1
-1Torrを越えると成形体の不純物成分の脱ガスが
不十分でとなるので好ましくなく、また昇温して140
0〜1550℃の範囲内の所定温度到達後の焼結炉内の
真空度および冷却時の焼結炉内の真空度を10-1Tor
r以下とした理由は、10-1Torrを越えると表面に
軟質な層が形成されて耐摩耗性が不十分でとなるので好
ましくないことによるものである。これら真空度の一層
好ましい範囲は、いずれも5×10-2Torr以下であ
る。
(E) Degree of vacuum The reason for heating while maintaining the inside of the sintering furnace at a vacuum of 10 -1 Torr or less at the time of raising the temperature during sintering is that the degree of vacuum in the sintering furnace is 1
If the pressure exceeds 0 -1 Torr, the degassing of the impurity component of the molded product becomes insufficient, which is not preferable.
The degree of vacuum in the sintering furnace after reaching a predetermined temperature in the range of 0 to 1550 ° C. and the degree of vacuum in the sintering furnace during cooling are set to 10 −1 Torr.
The reason for the lower limit of r is that when the pressure exceeds 10 -1 Torr, a soft layer is formed on the surface and the abrasion resistance becomes insufficient. The more preferable range of the degree of vacuum is 5 × 10 −2 Torr or less.

【0015】(f) 昇温時の窒素ガス導入条件 昇温時に1200〜1350℃の範囲内の所定温度に加
熱した時点で1〜60Torrの窒素ガスを導入するの
は、この時点で窒素ガスを1Torr未満導入しても脱
窒による内部ポアが生成し耐欠損性が不足するので好ま
しくないことによるものであり、一方、60Torrを
越えて窒素ガスを導入すると表面が激しく窒化し、耐摩
耗性が不足するので好ましくないことによるものであ
る。昇温時の窒素ガスを導入を1200〜1350℃の
範囲内の所定温度で行う理由は、1200℃未満では成
形体の不純物成分の脱ガスが不十分であるので好ましく
なく、一方、1350℃を越えると脱窒による内部ポア
が生成するので好ましくないことによるものである。昇
温時の窒素ガス導入の一層好ましい条件は、昇温時に1
250〜1300℃の範囲内の所定温度に加熱した時点
で10〜30Torrの窒素ガスを導入することであ
る。
(F) Nitrogen gas introduction condition at the time of temperature rise When heating to a predetermined temperature within the range of 1200 to 1350 ° C. at the time of temperature rise, the nitrogen gas of 1 to 60 Torr is introduced at this time. When introduced at less than 1 Torr, internal pores are formed due to denitrification and the fracture resistance is insufficient, which is not preferable. On the other hand, when nitrogen gas is introduced at more than 60 Torr, the surface is severely nitrided, resulting in poor wear resistance. This is because it is not desirable because it is insufficient. The reason why the nitrogen gas is introduced at a predetermined temperature within the range of 1200 to 1350 ° C. at the time of raising the temperature is less than 1200 ° C., because the degassing of the impurity component of the molded body is insufficient. If it exceeds, internal pores are generated due to denitrification, which is not preferable. More preferable conditions for introducing nitrogen gas at the time of temperature rise are as follows.
When heating to a predetermined temperature within the range of 250 to 1300 ° C., 10 to 30 Torr of nitrogen gas is introduced.

【0016】 (g) 加熱保持温度および窒素ガス再導入条件 1400〜1550℃の範囲内の所定温度に保持して焼
結炉内を10-1Torr以下の真空に戻し、引き続いて
焼結炉内を10-1Torr以下の真空雰囲気に保持しな
がら1400〜1550℃の範囲内の所定温度に保持し
た後、再び1〜20Torrの窒素ガスを導入して保持
するのは、1400℃未満では内部ポアが残存し、耐欠
損性が不足するので好ましくなく、一方、1550℃を
越えると硬質相が激しく成長し、耐欠損性が不足するの
で好ましくないことによるものである。1400〜15
50℃で再び1〜20Torrの窒素ガスを導入する理
由は、窒素ガスを1Torr未満の圧力で導入しても表
面を十分に窒化することができず、溶着現象が改善され
ないからであり、一方、20Torrを越えて窒素ガス
を導入すると、表面が激しく窒化し、耐摩耗性が不足す
るので好ましくないからである。加熱温度保持時の窒素
ガス導入条件の一層好ましい範囲は、1450〜150
0℃の範囲内の温度で5〜15Torrの窒素ガスを導
入することである。
(G) Heating holding temperature and nitrogen gas re-introduction condition The inside of the sintering furnace is returned to a vacuum of 10 -1 Torr or less by maintaining the temperature at a predetermined temperature in the range of 1400 to 1550 ° C. Is maintained at a predetermined temperature in the range of 1400 to 1550 ° C. while maintaining a vacuum atmosphere of 10 −1 Torr or less, and then nitrogen gas at 1 to 20 Torr is again introduced and maintained. This is not preferable because the residual hardening is insufficient because of the lack of fracture resistance. On the other hand, when the temperature exceeds 1550 ° C., the hard phase grows violently and the fracture resistance is insufficient. 1400-15
The reason why the nitrogen gas of 1 to 20 Torr is introduced again at 50 ° C. is that even if the nitrogen gas is introduced at a pressure of less than 1 Torr, the surface cannot be sufficiently nitrided and the welding phenomenon is not improved. If the nitrogen gas is introduced in excess of 20 Torr, the surface is severely nitrided and the wear resistance is insufficient, which is not preferable. The more preferable range of the nitrogen gas introduction condition at the time of holding the heating temperature is 1450 to 150
Introducing nitrogen gas at 5 to 15 Torr at a temperature in the range of 0 ° C.

【0017】[0017]

【発明の実施の形態】つぎに、この発明を実施例に基づ
いて具体的に説明する。原料粉末として、平均粒径:
1.4μmのTiCN(TiC/TiN=50/50)
粉末、平均粒径:1.5μmのTiC粉末、平均粒径:
1.0μmのTiN粉末、平均粒径:1.0μmのWC
粉末、平均粒径:1.5μmのMo2 C粉末、平均粒
径:2.0μmのVC粉末、平均粒径:1.3μmのN
bC粉末、平均粒径:1.2μmのTaC粉末、平均粒
径:1.5μmのZrC粉末、平均粒径:2.0μmの
Cr3 2 粉末、平均粒径:1.2μmのCo粉末、並
びに平均粒径:1.0μmのNi粉末を用意し、これら
原料粉末をそれぞれ表1に示される配合組成になるよう
に配合し、ボールミルにて72時間湿式混合し、乾燥し
た後、1.5ton/cm2 の圧力でCNMG12040
8形状にプレス成形することにより圧粉体A〜Fを作製
した。
Next, the present invention will be specifically described based on embodiments. As raw material powder, average particle size:
1.4 μm TiCN (TiC / TiN = 50/50)
Powder, average particle size: 1.5 μm TiC powder, average particle size:
1.0 μm TiN powder, average particle size: 1.0 μm WC
Powder, Mo 2 C powder with an average particle size of 1.5 μm, VC powder with an average particle size of 2.0 μm, N with an average particle size of 1.3 μm
bC powder, TaC powder having an average particle diameter of 1.2 μm, ZrC powder having an average particle diameter of 1.5 μm, Cr 3 C 2 powder having an average particle diameter of 2.0 μm, Co powder having an average particle diameter of 1.2 μm, In addition, Ni powder having an average particle diameter of 1.0 μm was prepared, and these raw material powders were blended so as to have a blending composition shown in Table 1, wet-mixed in a ball mill for 72 hours, dried, and then 1.5 ton. / Cm 2 at a pressure of CNMG12040
The green compacts A to F were prepared by press-forming into eight shapes.

【0018】[0018]

【表1】 [Table 1]

【0019】実施例1 これら表1に示される圧粉体A〜Fを焼結炉に装入し、
図2に示されるパターンの焼結条件で加熱した。図2に
おいて、aは昇温中の窒素導入温度、bは焼結温度、x
は昇温時の窒素ガス分圧、yは焼結温度に所定時間加熱
保持した後、再び窒素ガスを導入した時の窒素ガス分圧
を示し、図2におけるa、b、xおよびyの具体的数値
は表2に示した。
Example 1 The green compacts A to F shown in Table 1 were charged into a sintering furnace,
Heating was performed under the sintering conditions of the pattern shown in FIG. In FIG. 2, a is the nitrogen introduction temperature during heating, b is the sintering temperature, x
Represents the nitrogen gas partial pressure at the time of temperature rise, and y represents the nitrogen gas partial pressure when the nitrogen gas is introduced again after heating and holding at the sintering temperature for a predetermined time, and specific values of a, b, x and y in FIG. The target values are shown in Table 2.

【0020】[0020]

【表2】 [Table 2]

【0021】表1に示される圧粉体A〜Fを図2および
表2に示される条件で焼結し、ISO規格CNMG12
0408(無研磨級スローアウエイチップ)の形状を有
する本発明サーメット製切削工具(以下、本発明切削工
具という)1〜6を製造したのち、これら本発明切削工
具1〜6の逃げ面の垂直断面の焼き肌より内部へ2μm
(この点の濃度を最表面濃度と規定する)、5μm、
(以下、5μmおき)、・・・、200μm内部までE
PMAにより分析領域:2μm×200μmの定量分析
を行い、N、TiおよびW濃度の勾配極値深さ、Nおよ
びTiについては最表面濃度/極小値濃度値、並びにW
については最表面濃度/極大値濃度値を算出し、その結
果を表3に示した。なお、NおよびTiについてはNK
αとTiLlの重畳したX線スペクトルに波形分離法を
適用して分析を行った。
The green compacts A to F shown in Table 1 were sintered under the conditions shown in FIG.
After manufacturing cutting tools (hereinafter, referred to as the present invention cutting tools) 1 to 6 of the present invention having a shape of 0408 (non-polishing graded throwaway tip), a vertical section of a flank of the cutting tools 1 to 6 of the present invention is produced. 2μm inside from baked skin
(The density at this point is defined as the outermost surface density), 5 μm,
(Hereinafter, every 5 μm),..., Up to 200 μm
Quantitative analysis of analysis area: 2 μm × 200 μm was performed by PMA, and the extreme depth of the gradient of N, Ti and W concentrations, and the outermost surface concentration / minimum concentration value of N and Ti, and W
, The outermost surface concentration / maximum concentration value was calculated, and the results are shown in Table 3. For N and Ti, NK is used.
Analysis was performed by applying a waveform separation method to the X-ray spectrum in which α and TiLl were superimposed.

【0022】従来例1 一方、比較のために表1に示される圧粉体A〜Fを焼結
炉に装入し、この焼結炉内を表2に示される真空雰囲気
に保持しながら図2に示される温度パターンで表2に示
される温度で焼結したのち焼結炉の通電を切って、その
まま炉冷し、ISO規格CNMG120408(無研磨
級スローアウエイチップ)の形状を有する従来サーメッ
ト製切削工具(以下、従来切削工具という)1〜6を製
造し、得られた従来切削工具1〜6を実施例1と同様に
してEPMAにより分析領域:2μm×200μmの定
量分析を行い、N、TiおよびW濃度の勾配極値深さ、
NおよびTiについては最表面濃度/極小値濃度値、並
びにWについては最表面濃度/極大値濃度値を算出し、
その結果を表4に示した。
Conventional Example 1 On the other hand, for comparison, the green compacts A to F shown in Table 1 were charged into a sintering furnace, and the inside of the sintering furnace was maintained in a vacuum atmosphere shown in Table 2 while keeping the vacuum atmosphere. After sintering at the temperature shown in Table 2 according to the temperature pattern shown in Table 2, the sintering furnace was turned off, and the furnace was cooled as it was. Cutting tools (hereinafter, referred to as conventional cutting tools) 1 to 6 were manufactured, and the obtained conventional cutting tools 1 to 6 were subjected to quantitative analysis of an analysis area: 2 μm × 200 μm by EPMA in the same manner as in Example 1, and N, Gradient extreme depth of Ti and W concentration,
For N and Ti, the outermost surface concentration / minimum concentration value and for W, the outermost surface concentration / maximum concentration value are calculated,
Table 4 shows the results.

【0023】次に、本発明切削工具1〜6および従来切
削工具1〜6について、 被削材:SCM439、 切削速度:220m/min.、 送り:0.3mm/rev.、 切込み:2.5mm、 1パス:6秒切削−6秒休止、 の条件で50パスおよび100パスのインターバル切削
試験を行い、切刃の逃げ面摩耗量を測定し、それらの結
果を表3および表4に示し、溶着チッピングによる耐欠
損性を評価した。
Next, regarding the cutting tools 1 to 6 of the present invention and the conventional cutting tools 1 to 6, a work material: SCM439, a cutting speed: 220 m / min. Feed: 0.3 mm / rev. , Depth of cut: 2.5 mm, 1 pass: cutting for 6 seconds, pause for 6 seconds, an interval cutting test of 50 passes and 100 passes was performed, the flank wear of the cutting edge was measured, and the results are shown in Table 3. The results are shown in Table 4 and Table 4, and the chipping resistance due to welding chipping was evaluated.

【0024】[0024]

【表3】 [Table 3]

【0025】[0025]

【表4】 [Table 4]

【0026】表3〜表4に示された結果から、本発明切
削工具1〜6は、従来切削工具1〜6に比べて、耐摩耗
性を損なうこと無く、耐欠損性を向上させることができ
ることが分り、同一成分組成のサーメット製切削工具で
あっても、焼き肌表面部の相違によりサーメット製切削
工具の寿命が大いに改善されることが分かる。
From the results shown in Tables 3 and 4, the cutting tools 1 to 6 of the present invention can improve the chipping resistance without impairing the wear resistance as compared with the conventional cutting tools 1 to 6. It can be seen that even with cermet cutting tools having the same component composition, the life of the cermet cutting tool is greatly improved due to the difference in the burnt surface.

【0027】[0027]

【発明の効果】上述のように、この発明のサーメット製
切削工具は、従来よりも工具寿命を大幅に向上させるこ
とができ、産業上優れた効果を奏するものである。
As described above, the cutting tool made of cermet according to the present invention can greatly improve the tool life as compared with the conventional one, and has excellent industrial effects.

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

【図1】この発明のサーメット製切削工具および従来の
サーメット製切削工具の焼き肌表層部のN濃度、Ti濃
度、W濃度およびこれらの濃度分布を模擬的に示したグ
ラフである。
FIG. 1 is a graph schematically showing N concentration, Ti concentration, W concentration and distribution of these concentrations in the surface layer of a burnt surface of a cermet cutting tool of the present invention and a conventional cermet cutting tool.

【図2】この発明のサーメット製切削工具の焼結温度お
よび雰囲気条件を示すパターン図である。
FIG. 2 is a pattern diagram showing the sintering temperature and atmosphere conditions of the cermet cutting tool of the present invention.

───────────────────────────────────────────────────── フロントページの続き (72)発明者 野中 勝尚 茨城県結城郡石下町大字古間木1511番地 三菱マテリアル株式会社 筑波製作所 内 (72)発明者 中村 清一郎 茨城県結城郡石下町大字古間木1511番地 三菱マテリアル株式会社 筑波製作所 内 (72)発明者 辻崎 久史 茨城県結城郡石下町大字古間木1511番地 三菱マテリアル株式会社 筑波製作所 内 (56)参考文献 特開 平5−221725(JP,A) (58)調査した分野(Int.Cl.7,DB名) B23P 15/28 B23B 27/14 C22C 29/02 ──────────────────────────────────────────────────続 き Continuing on the front page (72) Inventor Katsuhisa Nonaka 1511 Komagi, Ishishita-cho, Yuki-gun, Ibaraki Prefecture Inside the Tsukuba Works, Mitsubishi Materials Corporation (72) Inventor Seiichiro Nakamura 1511 Furimagi, Ishishita-cho, Yuki-gun, Ibaraki Prefecture Mitsubishi Materials Corporation Tsukuba Works (72) Inventor Hisashi Tsujizaki 1511 Furamaki, Ishishita-cho, Yuki-gun, Ibaraki Prefecture Mitsubishi Materials Corporation Tsukuba Works (56) References JP-A-5-221725 58) Field surveyed (Int. Cl. 7 , DB name) B23P 15/28 B23B 27/14 C22C 29/02

Claims (1)

(57)【特許請求の範囲】(57) [Claims] 【請求項1】 Co粉末およびNi粉末の内の1種また
は2種:5〜25重量%を配合し、残りがTiの炭化
物、窒化物および炭窒化物粉末の内の1種または2種、
WC粉末、並びにMo、V、Nb、Ta、Zr、Crの
炭化物粉末の内の1種または2種以上を配合し、混合し
て得られた混合粉末をプレス成形して成形体を作製し、
この成形体を焼結するサーメット製切削工具の製造方法
において、 前記焼結は、焼結炉内の雰囲気を10-1Torr以下の
真空に保持しながら加熱し、1200〜1350℃の範
囲内の所定温度に加熱された時点で1〜60Torrの
窒素ガスを導入し、さらに加熱して1400〜1550
℃の範囲内の所定温度到達後ただちに焼結炉内の雰囲気
を10-1Torr以下の真空に戻し、引き続いて焼結炉
内を10-1Torr以下の真空雰囲気に保持しながら1
400〜1550℃の範囲内の所定温度に保持した後、
再び1〜20Torrの窒素ガスを導入して保持し、つ
いで冷却開始と同時に焼結炉内雰囲気を10-1Torr
以下の真空に戻すことを特徴とするサーメット製切削工
具の製造方法。
1. One or two of Co powder and Ni powder: 5 to 25% by weight, and the balance is one or two of Ti carbide, nitride and carbonitride powder,
WC powder, and one or more of carbide powders of Mo, V, Nb, Ta, Zr, and Cr are blended, and a mixed powder obtained by mixing is press-molded to form a molded body;
In the method of manufacturing a cermet cutting tool for sintering the formed body, the sintering is performed while heating the atmosphere in the sintering furnace while maintaining the atmosphere in a sintering furnace at a vacuum of 10 -1 Torr or less. When heated to a predetermined temperature, nitrogen gas at 1 to 60 Torr is introduced, and further heated to 1400 to 1550.
Immediately after reaching a predetermined temperature within the range of ° C., the atmosphere in the sintering furnace is returned to a vacuum of 10 -1 Torr or less, and subsequently, the atmosphere in the sintering furnace is maintained at a vacuum atmosphere of 10 -1 Torr or less.
After maintaining at a predetermined temperature in the range of 400 to 1550 ° C,
Nitrogen gas of 1 to 20 Torr is again introduced and maintained, and then, at the same time as cooling is started, the atmosphere in the sintering furnace is changed to 10 -1 Torr.
A method for manufacturing a cermet cutting tool, comprising returning the vacuum to the following:
JP01882996A 1996-02-05 1996-02-05 Cermet cutting tool with excellent fracture resistance and method of manufacturing the same Expired - Lifetime JP3317124B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP01882996A JP3317124B2 (en) 1996-02-05 1996-02-05 Cermet cutting tool with excellent fracture resistance and method of manufacturing the same

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP01882996A JP3317124B2 (en) 1996-02-05 1996-02-05 Cermet cutting tool with excellent fracture resistance and method of manufacturing the same

Publications (2)

Publication Number Publication Date
JPH09207005A JPH09207005A (en) 1997-08-12
JP3317124B2 true JP3317124B2 (en) 2002-08-26

Family

ID=11982465

Family Applications (1)

Application Number Title Priority Date Filing Date
JP01882996A Expired - Lifetime JP3317124B2 (en) 1996-02-05 1996-02-05 Cermet cutting tool with excellent fracture resistance and method of manufacturing the same

Country Status (1)

Country Link
JP (1) JP3317124B2 (en)

Also Published As

Publication number Publication date
JPH09207005A (en) 1997-08-12

Similar Documents

Publication Publication Date Title
EP1548136B1 (en) Cemented carbide insert and method of making the same
EP0368336A2 (en) Cermet blade member for cutting-tools and process for producing same
EP0515340A2 (en) Titanium based carbonitride alloy with binder phase enrichment
JP7272353B2 (en) Cemented Carbide, Cutting Tool and Cemented Carbide Manufacturing Method
EP1462534A1 (en) Compositionally graded sintered alloy and method of producing the same
JP5213326B2 (en) cermet
KR20060111103A (en) High toughness titanium carbonitride-based cermet and a manufacturing method thereof
JP5273987B2 (en) Cermet manufacturing method
JP2628200B2 (en) TiCN-based cermet and method for producing the same
JP4170402B2 (en) Titanium-based carbonitride alloy with nitrided surface region
JP3317124B2 (en) Cermet cutting tool with excellent fracture resistance and method of manufacturing the same
JP2775298B2 (en) Cermet tool
JPH0698540B2 (en) Method for manufacturing a cutting tool made of thermite with excellent wear resistance
JP3359221B2 (en) TiCN-based cermet tool and its manufacturing method
JPH0726172B2 (en) Toughness cermet and method for producing the same
JP2002292507A (en) Cutting tool made of cermet and its manufacturing method
JPH0530881B2 (en)
JP3103707B2 (en) Cermet for cutting tools
JP3366696B2 (en) Manufacturing method of high strength cermet
JP2503769B2 (en) A cutting tool made of cermet having excellent wear resistance and toughness, and a method for producing the same.
JP2814452B2 (en) Surface-finished sintered alloy, method for producing the same, and coated surface-finished sintered alloy obtained by coating the alloy with a hard film
JPH025811B2 (en)
JPH08246090A (en) Titanium carbon nitride base cermet excellent in toughness
JP3732866B2 (en) cermet
JP2004285421A (en) Cermet

Legal Events

Date Code Title Description
A02 Decision of refusal

Free format text: JAPANESE INTERMEDIATE CODE: A02

Effective date: 20020115

A01 Written decision to grant a patent or to grant a registration (utility model)

Free format text: JAPANESE INTERMEDIATE CODE: A01

Effective date: 20020514

FPAY Renewal fee payment (event date is renewal date of database)

Free format text: PAYMENT UNTIL: 20080614

Year of fee payment: 6

FPAY Renewal fee payment (event date is renewal date of database)

Free format text: PAYMENT UNTIL: 20090614

Year of fee payment: 7

FPAY Renewal fee payment (event date is renewal date of database)

Free format text: PAYMENT UNTIL: 20090614

Year of fee payment: 7

FPAY Renewal fee payment (event date is renewal date of database)

Free format text: PAYMENT UNTIL: 20100614

Year of fee payment: 8

FPAY Renewal fee payment (event date is renewal date of database)

Free format text: PAYMENT UNTIL: 20100614

Year of fee payment: 8

S531 Written request for registration of change of domicile

Free format text: JAPANESE INTERMEDIATE CODE: R313531

FPAY Renewal fee payment (event date is renewal date of database)

Free format text: PAYMENT UNTIL: 20100614

Year of fee payment: 8

R350 Written notification of registration of transfer

Free format text: JAPANESE INTERMEDIATE CODE: R350

FPAY Renewal fee payment (event date is renewal date of database)

Free format text: PAYMENT UNTIL: 20110614

Year of fee payment: 9

FPAY Renewal fee payment (event date is renewal date of database)

Free format text: PAYMENT UNTIL: 20120614

Year of fee payment: 10

FPAY Renewal fee payment (event date is renewal date of database)

Free format text: PAYMENT UNTIL: 20120614

Year of fee payment: 10

FPAY Renewal fee payment (event date is renewal date of database)

Free format text: PAYMENT UNTIL: 20130614

Year of fee payment: 11

EXPY Cancellation because of completion of term