JP2004181555A - Surface-coated cermet cutting tool with hard coating layer excellent in thermal shock resistance and surface lubricatability - Google Patents

Surface-coated cermet cutting tool with hard coating layer excellent in thermal shock resistance and surface lubricatability Download PDF

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JP2004181555A
JP2004181555A JP2002349646A JP2002349646A JP2004181555A JP 2004181555 A JP2004181555 A JP 2004181555A JP 2002349646 A JP2002349646 A JP 2002349646A JP 2002349646 A JP2002349646 A JP 2002349646A JP 2004181555 A JP2004181555 A JP 2004181555A
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layer
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hard coating
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thickness
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Toshiaki Ueda
稔晃 植田
Takatoshi Oshika
高歳 大鹿
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Mitsubishi Materials Corp
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Mitsubishi Materials Corp
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Abstract

<P>PROBLEM TO BE SOLVED: To provide a surface-coated cermet cutting tool with hard coating layer excellent in thermal shock resistance. <P>SOLUTION: This surface-coated cermet cutting tool has a hard coating layer constituted of (a) to (c) on a surface of a tool base body constituted of WC group cemented carbide and TiCN group cermet: (a) A lower layer having average layer thickness of 3 to 20 μm, and constituted of a Ti compound layer constituted of lamination layers of one layer or more than two layers among a TiC layer, a TiN layer, a TiCN layer, a TiCO layer and a TiCNO layer which are all evaporated and formed; (b) An upper layer having average layer thickness of 3 to 15 μm, constituted of an α type crystal structure of a crystal structure by applying heating transforming treatment to Al<SB>2</SB>O<SB>3</SB>having a κ type or θ type crystal structure in a state of being evaporated and formed, and also constituted of a heating transformed α type Al<SB>2</SB>O<SB>3</SB>layer having a structure of dispersing-distributing a heating transformed crack. (c) A surface layer having average layer thickness of 0.1 to 5 μm, and constituted of a Ti oxide layer for satisfying 1.2 to 1.9 in the atomic ratio of X to Ti by measuring a thickness directional central part by an Auger spectral analyzer when expressed by a composition formula : TiOx. <P>COPYRIGHT: (C)2004,JPO&NCIPI

Description

【0001】
【発明の属する技術分野】
この発明は、鋼や鋳鉄などの高速断続切削時に切刃部にきわめて短いピッチで繰り返し付加される熱衝撃に対して硬質被覆層がすぐれた耐熱衝撃性を示し、さらに特にステンレス鋼や軟鋼などのきわめて粘性が高く、かつ切粉が切刃表面に溶着し易い難削材の高速断続切削加工でも、硬質被覆層が切粉に対してすぐれた表面潤滑性を示すことから、通常の鋼や鋳鉄は勿論のこと、ステンレス鋼や軟鋼などの難削材の高速断続切削加工に用いた場合に、切刃にチッピング(微小欠け)などの発生なく、すぐれた切削性能を長期に亘って発揮する表面被覆サーメット製切削工具(以下、被覆サーメット工具という)に関するものである。
【0002】
【従来の技術】
従来、一般に、炭化タングステン(以下、WCで示す)基超硬合金または炭窒化チタン(以下、TiCNで示す)基サーメットで構成された基体(以下、これらを総称して工具基体という)の表面に、
(a)下部層として、3〜20μmの平均層厚を有し、いずれも化学蒸着形成および/または物理蒸着形成(以下、単に蒸着形成という)されたTiの炭化物(以下、TiCで示す)層、窒化物(以下、同じくTiNで示す)層、炭窒化物(以下、TiCNで示す)層、炭酸化物(以下、TiCOで示す)層、および炭窒酸化物(以下、TiCNOで示す)層のうちの1層または2層以上の積層からなるTi化合物層、
(b)上部層として、3〜15μmの平均層厚を有し、かつ結晶構造がα型および/またはκ型の蒸着形成された酸化アルミニウム(以下、Al23で示す)層、
以上(a)および(b)で構成された硬質被覆層を蒸着形成してなる被覆サーメット工具が知られており、この被覆サーメット工具が、例えば各種の鋼や鋳鉄などの連続切削や断続切削に用いられていることも知られている(例えば、特許文献1参照)。
【0003】
また、一般に、上記の被覆サーメット工具の硬質被覆層を構成するTi化合物層やAl23 層が粒状結晶組織を有し、さらに、前記Ti化合物層を構成するTiCN層を、層自身の強度向上を目的として、通常の化学蒸着装置にて、反応ガスとして有機炭窒化物を含む混合ガスを使用し、700〜950℃の中温温度域で化学蒸着することにより形成して縦長成長結晶組織をもつようにすることも知られている(例えば、特許文献2参照)。
【0004】
【特許文献1】
特開平6−31503号公報
【特許文献2】
特開平6−8010号公報
【0005】
【発明が解決しようとする課題】
近年の切削装置の高性能化はめざましく、一方で切削加工に対する省力化および省エネ化、さらに低コスト化の要求は強く、これに伴い、切削加工は一段と高速化の傾向にあるが、上記の従来被覆サーメット工具においては、これを鋼や鋳鉄などの通常の条件での連続切削や断続切削に用いた場合には問題はないが、特にこれを切削条件の最も厳しい高速断続切削、すなわち切刃部にきわめて短いピッチで繰り返し熱衝撃が付加される高速断続切削に用いた場合、硬質被覆層の上部層を構成するAl23層は、硬質で耐熱性にすぐれるものの、熱衝撃に脆いために、硬質被覆層にはチッピング(微小欠け)が発生し易く、さらにきわめて粘性の高いステンレス鋼や軟鋼などの被削材の高速断続切削では、これら被削材の切粉は、硬質被覆層を構成する特にAl23層に対する親和性が高いために、切刃表面に溶着し易く、この溶着現象が前記の繰り返し熱衝撃現象と相俟って、切刃には一段とチッピングが発生し易くなり、この結果比較的短時間で使用寿命に至るのが現状である。
【0006】
【課題を解決するための手段】
そこで、本発明者等は、上述のような観点から、上記のステンレス鋼や軟鋼などのきわめて粘性が高く、かつ切粉が切刃表面に溶着し易い難削材の高速断続切削加工でも、切刃がすぐれた耐チッピング性を発揮する被覆サーメット工具を開発すべく研究を行った結果、
工具基体の表面に、下部層として、通常の条件で、上記Ti化合物層を形成した後、同じく通常の条件で、結晶構造がκ型またはθ型のAl23層を蒸着形成し、この状態で加熱処理、望ましくはAr雰囲気中、温度:1000℃以上で所定時間保持の条件で加熱処理を施すと、前記κ型またはθ型の結晶構造はα型結晶構造に変態し、かつ加熱変態生成クラックが層中に分散分布した組織を有するようになるが、この結果の加熱変態α型Al23層を上部層とし、この上部層の表面に、
反応ガス組成を、体積%で、
TiCl4:0.2〜10%、
CO2:0.1〜10%、
Ar:5〜60%、
2:残り、
とし、かつ、
反応雰囲気温度:800〜1100℃、
反応雰囲気圧力:4〜70kPa(30〜525torr)、
とした条件で、0.1〜5μmの平均層厚を有し、かつ、厚さ方向中央部をオージェ分光分析装置で測定して、Tiに対する酸素の割合が原子比で1.2〜1.9、即ち、
組成式:TiOX
で表わした場合、
X:Tiに対する原子比で1.2〜1.9、
を満足するTi酸化物層を表面層として蒸着形成すると、このTi酸化物層は、前記加熱変態α型Al23層との界面でこれの加熱変態生成クラック中に十分に入り込んで前記加熱変態生成クラックを著しく安定化した状態に保持するばかりでなく、ステンレス鋼や軟鋼などの粘性の高い難削材に対する親和性がきわめて低く、これは高い発熱を伴う高速切削加工でも変わらない性質をもつことから、硬質被覆層の下部層が上記Ti化合物層で構成され、同上部層および表面層が上記の加熱変態α型Al23層およびTi酸化物層で構成された被覆サーメット工具においては、前記上部層を構成する加熱変態α型Al23層中に分散分布する加熱変態生成クラックが、特に高速断続切削時の激しい熱衝撃を吸収して、これを緩和し、さらに前記表面層のTi酸化物層は切粉が溶着し難い性質、すなわちすぐれた表面潤滑性を有することから、硬質被覆層におけるチッピング発生が著しく抑制されるようになるという研究結果を得たのである。
【0007】
この発明は、上記の研究結果に基づいてなされたものであって、WC基超硬合金またはTiCN基サーメットで構成された工具基体の表面に、
(a)下部層として、3〜20μmの平均層厚を有し、いずれも蒸着形成されたTiC層、TiN層、TiCN層、TiCO層、およびTiCNO層のうちの1層または2層以上の積層からなるTi化合物層、
(b)上部層として、3〜15μmの平均層厚を有し、蒸着形成した状態でκ型またはθ型の結晶構造を有するAl23に加熱変態処理を施して結晶構造をα型結晶構造とし、かつ加熱変態生成クラックが分散分布した組織を有する加熱変態α型Al23層、
(c)表面層として、0.1〜5μmの平均層厚を有し、かつ、
組成式:TiOX
で表わした場合、厚さ方向中央部をオージェ分光分析装置で測定して、
X:Tiに対する原子比で1.2〜1.9、
を満足するTi酸化物層、
以上(a)〜(c)で構成された硬質被覆層を形成してなる、硬質被覆層がすぐれた耐熱衝撃性および表面潤滑性を有する被覆サーメット工具に特徴を有するものである。
【0008】
つぎに、この発明の被覆サーメット工具の硬質被覆層の構成層の平均層厚を上記の通りに限定した理由を説明する。
(a)下部層(Ti化合物層)
Ti化合物層は、自体が強度を有し、これの存在によって硬質被覆層が強度を具備するようになるほか、工具基体と上部層である加熱変態α型Al23層のいずれにも強固に密着し、よって硬質被覆層の工具基体に対する密着性向上に寄与する作用をもつが、その平均層厚が3μm未満では、前記作用を十分に発揮させることができず、一方その平均層厚が20μmを越えると、特に高熱発生を伴なう高速断続切削で熱塑性変形を起し易くなり、これが偏摩耗の原因となることから、その平均層厚を3〜20μmと定めた。
【0009】
(b)上部層(加熱変態α型Al23層)
加熱変態α型Al23層には、Al23自体のもつ高硬度とすぐれた耐熱性によって硬質被覆層の耐摩耗性を向上させるとともに、上記の通り層中に分散分布する加熱変態生成クラックの作用で熱衝撃を吸収して、硬質被覆層にチッピングが発生するのを著しく抑制する作用があるが、その平均層厚が3μm未満では、前記作用を十分に発揮させることができず、一方その平均層厚が15μmを越えて厚くなりすぎると、前記加熱変態生成クラックがチッピング発生の原因となることから、その平均層厚を3〜15μmと定めた。
【0010】
(c)表面層(Ti酸化物層)
Ti酸化物層は、上記の通り加熱変態α型Al23層との界面でこれの加熱変態生成クラック中に十分に入り込んで前記加熱変態生成クラックを著しく安定化した状態に保持し、もって前記加熱変態α型Al23層によってもたらされる耐熱衝撃性の向上を十分に発揮させるようにする作用をもつほか、すぐれた表面潤滑性を有するが、その平均層厚が0.1μm未満では、前記加熱変態α型Al23層中の加熱変態生成クラックの安定化が不十分であるばかりでなく、所望の表面潤滑性を確保することができないことから、チッピングが発生し易くなり、一方前記Ti酸化物層による前記作用は5μmまでの平均層厚で十分であり、経済性を考慮して、その平均層厚を0.1〜5μmと定めた。
【0011】
また、この発明の被覆サーメット工具において、表面層を構成するTi酸化物層における酸素(O)のTiに対する原子比(X値)を1.2〜1.9としたのは、その値が1.2未満では所望のすぐれた表面潤滑性を確保することができず、一方その値が1.9を越えると、層中に気孔が形成され易くなり、健全な表面層の安定的形成が難しくなるという理由によるものである。
【0012】
さらに、この発明の被覆サーメット工具の硬質被覆層を構成するTi酸化物層をX線回折により観察したところ、組成式:TiOXのX値に対応して、Ti23、Ti35、Ti47、およびTi59などのうちの少なくともいずれかに主要ピークが現れる回折パターンを示し、これらの回折結果から前記Ti酸化物層はMagneli相と呼ばれるものからなり、一般的にTin2n-1で表わされるものであることが明らかである。
【0013】
【発明の実施の形態】
つぎに、この発明の被覆サーメット工具を実施例により具体的に説明する。
原料粉末として、いずれも1〜3μmの平均粒径を有するWC粉末、TiC粉末、ZrC粉末、VC粉末、TaC粉末、NbC粉末、Cr3 2 粉末、TiN粉末、TaN粉末、およびCo粉末を用意し、これら原料粉末を、表1に示される配合組成に配合し、さらにワックスを加えてアセトン中で24時間ボールミル混合し、減圧乾燥した後、98MPaの圧力で所定形状の圧粉体にプレス成形し、この圧粉体を5Paの真空中、1370〜1470℃の範囲内の所定の温度に1時間保持の条件で真空焼結し、焼結後、切刃部にR:0.07mmのホーニング加工を施すことによりISO・CNMG120408に規定するスローアウエイチップ形状をもったWC基超硬合金製の工具基体A〜Fをそれぞれ製造した。
【0014】
また、原料粉末として、いずれも0.5〜2μmの平均粒径を有するTiCN(質量比でTiC/TiN=50/50)粉末、Mo2 C粉末、ZrC粉末、NbC粉末、TaC粉末、WC粉末、Co粉末、およびNi粉末を用意し、これら原料粉末を、表2に示される配合組成に配合し、ボールミルで24時間湿式混合し、乾燥した後、98MPaの圧力で圧粉体にプレス成形し、この圧粉体を1.3kPaの窒素雰囲気中、温度:1540℃に1時間保持の条件で焼結し、焼結後、切刃部分にR:0.07mmのホーニング加工を施すことによりISO規格・CNMG120412のチップ形状をもったTiCN基サーメット製の工具基体a〜fを形成した。
【0015】
ついで、これらの工具基体A〜Fおよび工具基体a〜fの表面に、通常の化学蒸着装置を用い、表3(表3中のl−TiCNは特開平6−8010号公報に記載される縦長成長結晶組織をもつTiCN層の形成条件を示すものであり、これ以外は通常の粒状結晶組織の形成条件を示すものである)に示される条件にて、表4に示される目標層厚のTi化合物層を硬質被覆層の下部層として蒸着形成し、ついで同じく表3に示される条件で結晶構造がκ型またはθ型のAl23層を蒸着形成し、これにAr雰囲気中、温度:1050℃に2〜10時間の範囲内の所定時間保持の条件で加熱変態処理を施して、前記κ型またはθ型の結晶構造をα型に変態させて、加熱変態生成クラックが層中に分散分布した加熱変態α型Al23層を同じく表5に示される目標層厚で硬質被覆層の上部層として形成し、さらに同じく表4に示される条件で、かつ表5に示される目標層厚のTi酸化物層を同表面層として形成することにより本発明被覆サーメット工具1〜12をそれぞれ製造した。
また、比較の目的で、表6に示される通り、硬質被覆層の上部層を同じく表6に示される平均層厚の蒸着α型Al23層とし、かつ表面層の形成を行なわない以外は同一の条件で従来被覆サーメット工具1〜12をそれぞれ製造した。
【0016】
さらに、上記の本発明被覆サーメット工具と従来被覆サーメット工具の硬質被覆層を構成する加熱変態α型Al23層と蒸着α型Al23層の相違を観察する目的でX線回折を測定した。
これらのX線回折の測定は、X線回折チャート上で(001)面および(002)面にのみ回折ピークが現れる単結晶WCを基体試料として用い、この基体試料の表面に、本発明被覆サーメット工具3、7、および11の目標層厚が15μm、10μm、および5μmの加熱変態α型Al23層、並びに従来被覆サーメット工具3、7、および11の同じく目標層厚が15μm、10μm、および5μmの蒸着α型Al23層の形成条件と同一の条件で、それぞれ目標層厚が15μm、10μm、および5μmの加熱変態α型Al23層および蒸着α型Al23層を直接形成して本発明被覆試料A〜Cおよび従来被覆試料a〜cを製造し、これら被覆試料の前記加熱変態α型Al23層および蒸着α型Al23層のX線回折を測定することにより行なった。この測定結果を図1〜6に示した。
本発明被覆試料A〜Cの加熱変態α型Al23層のX線回折チャートを示す図1〜3と、従来被覆試料a〜cの蒸着α型Al23層のX線回折チャートを示す図4〜6の比較から、前記加熱変態α型Al23層では(006)面および(018)面に明確な回折ピークが現れているのに対して、前記蒸着α型Al23層ではこれら(006)面および(018)面に回折ピークは存在しないことが明かである。
さらに、上記の単結晶WCで構成された基体試料の表面に、それぞれ目標層厚が15μm、10μm、および5μmの加熱変態α型Al23層および蒸着α型Al23層を直接形成してなる本発明被覆試料A〜Cおよび従来被覆試料a〜cの前記加熱変態α型Al23層および蒸着α型Al23層のそれぞれについて、基体試料表面と平行な研磨表面における結晶面の電子線後方散乱回折(EBSD)を、熱電界放射型走査電子顕微鏡(日本電子(株)製)および方位回折装置(テクセム・ラボラトリース(株)製)を用いて行なったところ、前記加熱変態α型Al23層では、いずれも結晶方位マップが濃い赤色の色調を示し、これはAl23の結晶構造である六方晶の(0001)面(六角形の平行面)が前記Al23層表面(基体試料表面)に対して平行にきわめて強く配向していることを示し、一方前記蒸着α型Al23層では、いずれも結晶方位マップに緑色や青色、さらに黄色およびピンク色など様々な色調が現れ、これは六方晶を構成する結晶面に特定の配向性が存在しないことを示すものである。
【0017】
また、この結果得られた本発明被覆サーメット工具1〜12および従来被覆サーメット工具1〜12について、これの硬質被覆層の構成層を走査型電子顕微鏡を用いて観察(層の縦断面を観察)したところ、前者ではいずれもTi化合物層、加熱変態生成クラックが層中に分散分布した加熱変態α型Al23層、およびTi酸化物層からなり、後者では、いずれもTi化合物と蒸着α型Al23層からなることが確認された。
さらに、上記の本発明被覆サーメット工具1〜12の表面層について、その厚さ方向中央部の酸素含有割合(X値)をオージェ分光分析装置を用いて測定したところ、表4に示される目標値と実質的に同じ値を示した。
また、これらの被覆サーメット工具の硬質被覆層の構成層の厚さを、走査型電子顕微鏡を用いて測定(同じく縦断面測定)したところ、いずれも目標層厚と実質的に同じ平均層厚(5点測定の平均値)を示した。
【0018】
つぎに、上記の各種の被覆サーメット工具をいずれも工具鋼製バイトの先端部に固定治具にてネジ止めした状態で、本発明被覆サーメット工具1〜6および従来被覆サーメット工具1〜6については、
被削材:JIS・SUS304の長さ方向等間隔4本縦溝入り丸棒、
切削速度:400m/min、
切り込み:1.0mm、
送り:0.15mm/rev、
切削時間:3分、
の条件でのステンレス鋼の乾式高速断続切削試験、
被削材:JIS・S15Cの長さ方向等間隔4本縦溝入り丸棒、
切削速度:450m/min、
切り込み:1.5mm、
送り:0.2mm/rev、
切削時間:3分、
の条件での軟鋼の乾式高速断続切削試験を行った。
【0019】
さらに、本発明被覆サーメット工具7〜12および従来被覆サーメット工具7〜12については、
被削材:JIS・SUS304の長さ方向等間隔4本縦溝入り丸棒、
切削速度:400m/min、
切り込み:0.5mm、
送り:0.15mm/rev、
切削時間:3分、
の条件でのステンレス鋼の乾式高速断続切削試験、
被削材:JIS・S15Cの長さ方向等間隔4本縦溝入り丸棒、
切削速度:450m/min、
切り込み:1.0mm、
送り:0.15mm/rev、
切削時間:3分、
の条件での軟鋼の乾式高速断続切削試験を行い、いずれの切削試験でも切刃の逃げ面摩耗幅を測定した。この測定結果を表7に示した。
【0020】
【表1】

Figure 2004181555
【0021】
【表2】
Figure 2004181555
【0022】
【表3】
Figure 2004181555
【0023】
【表4】
Figure 2004181555
【0024】
【表5】
Figure 2004181555
【0025】
【表6】
Figure 2004181555
【0026】
【表7】
Figure 2004181555
【0027】
【発明の効果】
表5〜7に示される結果から、本発明被覆サーメット工具1〜12は、硬質被覆層の上部層を構成する加熱変態α型Al23層中に分散分布する加熱変態生成クラックによるすぐれた熱衝撃吸収性および表面層のTi酸化物層のもつ切粉に対するすぐれた表面潤滑性の作用で、熱衝撃がきわめて高く、かつ高い発熱を伴なうステンレス鋼や軟鋼の高速断続切削でも、切刃のチッピング発生が著しく抑制され、すぐれた耐摩耗性を発揮するのに対して、硬質被覆層の上部層が蒸着α型Al23層からなる従来被覆サーメット工具1〜12においては、高速断続切削では前記蒸着α型Al23層が激しい熱衝撃に耐えられず、かつ被削材がステンレス鋼や軟鋼などのきわめて粘性が高く、かつ切粉が切刃表面に溶着し易い難削材であることと相俟って、切刃にチッピングが発生し、比較的短時間で使用寿命に至ることが明らかである。
上述のように、この発明の被覆サーメット工具は、通常の条件での連続切削や断続切削は勿論のこと、特に熱衝撃がきわめて高く、かつ高い発熱を伴なう切削条件の最も厳しい難削材の高速断続切削でもすぐれた耐チッピング性を示し、長期に亘ってすぐれた切削性能を発揮するものであるから、切削装置の高性能化並びに切削加工の省力化および省エネ化、さらに低コスト化に十分満足に対応できるものである。
【図面の簡単な説明】
【図1】本発明被覆サーメット工具3の硬質被覆層を構成する加熱変態α型Al23層(目標層厚:15μm)のX線回折チャートを示す図である。
【図2】本発明被覆サーメット工具7の硬質被覆層を構成する加熱変態α型Al23層(目標層厚:10μm)のX線回折チャートを示す図である。
【図3】本発明被覆サーメット工具11の硬質被覆層を構成する加熱変態α型Al23層(目標層厚:5μm)のX線回折チャートを示す図である。
【図4】従来被覆サーメット工具3の硬質被覆層を構成する蒸着α型Al23層(目標層厚:15μm)のX線回折チャートを示す図である。
【図5】従来被覆サーメット工具7の硬質被覆層を構成する蒸着α型Al23層(目標層厚:10μm)のX線回折チャートを示す図である。
【図6】従来被覆サーメット工具11の硬質被覆層を構成する蒸着α型Al23層(目標層厚:5μm)のX線回折チャートを示す図である。[0001]
TECHNICAL FIELD OF THE INVENTION
The present invention provides a hard coating layer that exhibits excellent thermal shock resistance to thermal shock repeatedly applied to the cutting edge at an extremely short pitch during high-speed interrupted cutting of steel, cast iron, etc., and more particularly, for stainless steel and mild steel. Even in high-speed interrupted cutting of difficult-to-cut materials that are extremely viscous and chips easily adhere to the cutting edge surface, the hard coating layer shows excellent surface lubricity against chips, so ordinary steel and cast iron Needless to say, when used for high-speed intermittent cutting of difficult-to-cut materials such as stainless steel and mild steel, surfaces that exhibit excellent cutting performance over a long period of time without chipping (small chipping) on the cutting edge The present invention relates to a coated cermet cutting tool (hereinafter, referred to as a coated cermet tool).
[0002]
[Prior art]
2. Description of the Related Art Conventionally, generally, a substrate (hereinafter, these are collectively referred to as a tool substrate) formed of a tungsten carbide (hereinafter, referred to as WC) -based cemented carbide or a titanium cermet (hereinafter, referred to as TiCN) -based cermet is generally provided on a surface of the substrate. ,
(A) As a lower layer, a layer of Ti carbide (hereinafter referred to as TiC) having an average layer thickness of 3 to 20 μm, all of which are formed by chemical vapor deposition and / or physical vapor deposition (hereinafter simply referred to as vapor deposition). , A nitride (hereinafter also referred to as TiN) layer, a carbonitride (hereinafter referred to as TiCN) layer, a carbonate (hereinafter referred to as TiCO) layer, and a carbonitride (hereinafter referred to as TiCNO) layer A Ti compound layer composed of one or two or more layers,
(B) an aluminum oxide (hereinafter referred to as Al 2 O 3 ) layer having an average layer thickness of 3 to 15 μm and having an α-type and / or κ-type crystal structure as an upper layer;
A coated cermet tool formed by vapor-depositing a hard coating layer composed of (a) and (b) above is known, and this coated cermet tool can be used for continuous cutting or intermittent cutting of various types of steel or cast iron, for example. It is also known that it is used (for example, see Patent Document 1).
[0003]
In general, the Ti compound layer and the Al 2 O 3 layer constituting the hard coating layer of the above-mentioned coated cermet tool have a granular crystal structure, and further, the TiCN layer constituting the Ti compound layer is provided with the strength of the layer itself. For the purpose of improvement, using a mixed gas containing an organic carbonitride as a reaction gas in a normal chemical vapor deposition apparatus, a chemical vapor deposition is performed at a medium temperature range of 700 to 950 ° C. to form a vertically grown crystal structure. It is also known to have it (see, for example, Patent Document 2).
[0004]
[Patent Document 1]
JP-A-6-31503 [Patent Document 2]
JP-A-6-8010 [0005]
[Problems to be solved by the invention]
In recent years, the performance of cutting equipment has been remarkably improved, but on the other hand, there has been a strong demand for labor saving, energy saving, and further cost reduction for cutting work.Accordingly, cutting work has tended to be further accelerated. In the case of coated cermet tools, there is no problem if this is used for continuous cutting or interrupted cutting under ordinary conditions such as steel or cast iron. When used for high-speed interrupted cutting, in which thermal shock is repeatedly applied at a very short pitch, the upper layer of the hard coating layer, the Al 2 O 3 layer, is hard and has excellent heat resistance, but is brittle to thermal shock. In addition, chipping (small chipping) easily occurs in the hard coating layer, and in high-speed interrupted cutting of work materials such as stainless steel and mild steel having extremely high viscosity, the chips of these work materials are hard coated layer. Because of the high affinity for the particular the Al 2 O 3 layer constituting, easily welded to the cutting edge surface, I the welding behavior the repeated thermal shock phenomenon coupled with the liable further chipping occurs in the cutting edge As a result, at present, the service life is reached in a relatively short time.
[0006]
[Means for Solving the Problems]
In view of the above, the inventors of the present invention have proposed cutting, even in high-speed intermittent cutting of difficult-to-cut materials such as the above-mentioned stainless steel and mild steel, which are extremely viscous and in which cutting chips easily adhere to the cutting blade surface. As a result of conducting research to develop a coated cermet tool with excellent chipping resistance,
After forming the Ti compound layer as a lower layer on the surface of the tool base under ordinary conditions, an Al 2 O 3 layer having a κ-type or θ-type crystal structure is formed by vapor deposition under the same general conditions. When heat treatment is performed in this state, preferably in an Ar atmosphere at a temperature of 1000 ° C. or higher and maintained for a predetermined time, the κ-type or θ-type crystal structure is transformed into an α-type crystal structure, and the heat transformation is performed. The generated cracks have a structure dispersed and distributed in the layer, and the resulting heat-transformed α-type Al 2 O 3 layer is used as an upper layer, and the surface of this upper layer is
The reaction gas composition, by volume%,
TiCl 4: 0.2~10%,
CO 2 : 0.1 to 10%,
Ar: 5 to 60%,
H 2 : rest,
And
Reaction atmosphere temperature: 800 to 1100 ° C,
Reaction atmosphere pressure: 4 to 70 kPa (30 to 525 torr),
Under the conditions described above, the layer has an average layer thickness of 0.1 to 5 μm, and the center in the thickness direction is measured by an Auger spectroscopic analyzer, and the ratio of oxygen to Ti is 1.2 to 1. 9, that is,
Composition formula: TiO x ,
When represented by
X: 1.2 to 1.9 in atomic ratio to Ti;
Is formed as a surface layer by evaporation, the Ti oxide layer sufficiently penetrates into the heat transformation generation crack at the interface with the heat transformation α-type Al 2 O 3 layer, and In addition to maintaining the transformation-generated cracks in a significantly stabilized state, it has a very low affinity for highly viscous and difficult-to-cut materials such as stainless steel and mild steel, which has the same properties as high-speed cutting with high heat generation. Therefore, in the coated cermet tool in which the lower layer of the hard coating layer is composed of the Ti compound layer, and the upper layer and the surface layer are composed of the above-mentioned heat-transformed α-type Al 2 O 3 layer and the Ti oxide layer. , the heating transformation α-type Al 2 O 3 heat transformation product cracks disperse distribution in the layer constituting the upper layer, in particular absorb severe thermal shock during high-speed intermittent cutting, and alleviate this, further Since the Ti oxide layer of the surface layer has a property that chips are not easily welded, that is, it has excellent surface lubricating properties, a research result was obtained that the occurrence of chipping in the hard coating layer was significantly suppressed. .
[0007]
The present invention has been made on the basis of the above research results, and has a tool base formed of a WC-based cemented carbide or a TiCN-based cermet,
(A) The lower layer has an average layer thickness of 3 to 20 μm, and is a stack of one or more of a TiC layer, a TiN layer, a TiCN layer, a TiCO layer, and a TiCNO layer, all of which are formed by vapor deposition. A Ti compound layer comprising:
(B) As an upper layer, Al 2 O 3 having an average layer thickness of 3 to 15 μm and having a κ-type or θ-type crystal structure in a vapor-deposited state is subjected to a heat transformation treatment to change the crystal structure to an α-type crystal. A heating transformation α-type Al 2 O 3 layer having a structure and a structure in which heating transformation generation cracks are dispersed and distributed,
(C) the surface layer has an average layer thickness of 0.1 to 5 μm, and
Composition formula: TiO x ,
When represented by, the center in the thickness direction is measured with an Auger spectrometer,
X: 1.2 to 1.9 in atomic ratio to Ti;
A Ti oxide layer that satisfies
The present invention is characterized by a coated cermet tool having a hard coating layer formed of the above (a) to (c) and having excellent thermal shock resistance and surface lubricity.
[0008]
Next, the reason why the average thickness of the constituent layers of the hard coating layer of the coated cermet tool of the present invention is limited as described above will be described.
(A) Lower layer (Ti compound layer)
The Ti compound layer itself has strength, and the presence of the Ti compound layer allows the hard coating layer to have strength. In addition, the Ti compound layer is firmly attached to both the tool base and the heating-transformed α-type Al 2 O 3 layer as the upper layer. Has a function of contributing to the improvement of the adhesion of the hard coating layer to the tool base, but if the average layer thickness is less than 3 μm, the above effect cannot be sufficiently exerted. If it exceeds 20 μm, it becomes easy to cause thermoplastic deformation especially in high-speed interrupted cutting accompanied by high heat generation, which causes uneven wear. Therefore, the average layer thickness is set to 3 to 20 μm.
[0009]
(B) Upper layer (heat-transformed α-type Al 2 O 3 layer)
The heat-transformed α-type Al 2 O 3 layer enhances the wear resistance of the hard coating layer due to the high hardness and excellent heat resistance of the Al 2 O 3 itself, as well as the heat transformation dispersed and distributed in the layer as described above. The effect of the generated cracks absorbs the thermal shock and has the effect of significantly suppressing the occurrence of chipping in the hard coating layer. However, if the average layer thickness is less than 3 μm, the above effect cannot be sufficiently exerted. On the other hand, if the average layer thickness exceeds 15 μm and becomes too thick, the cracks generated by the heat transformation may cause chipping. Therefore, the average layer thickness is set to 3 to 15 μm.
[0010]
(C) Surface layer (Ti oxide layer)
As described above, the Ti oxide layer penetrates sufficiently into the heat transformation-generated cracks at the interface with the heat-transformed α-type Al 2 O 3 layer to maintain the heat-transformed cracks in a significantly stabilized state. In addition to having the effect of sufficiently exhibiting the improvement in thermal shock resistance brought about by the above-mentioned heat-transformed α-type Al 2 O 3 layer, it also has excellent surface lubricity, but if the average layer thickness is less than 0.1 μm, The stabilization of the heat transformation generation cracks in the heat transformation α-type Al 2 O 3 layer is not only insufficient, but the desired surface lubricity cannot be secured, so that chipping is likely to occur, On the other hand, the effect of the Ti oxide layer is sufficient when the average layer thickness is up to 5 μm, and the average layer thickness is determined to be 0.1 to 5 μm in consideration of economy.
[0011]
In the coated cermet tool of the present invention, the atomic ratio (X value) of oxygen (O) to Ti in the Ti oxide layer constituting the surface layer is set to 1.2 to 1.9, because the value is 1 to 1. If it is less than 0.2, the desired excellent surface lubricating property cannot be secured, while if it exceeds 1.9, pores are easily formed in the layer, and it is difficult to form a sound surface layer stably. It is because it becomes.
[0012]
Further, when the Ti oxide layer constituting the hard coating layer of the coated cermet tool of the present invention was observed by X-ray diffraction, Ti 2 O 3 and Ti 3 O 5 were obtained in accordance with the X value of the composition formula: TiO X. , Ti 4 O 7 , and Ti 5 O 9 show a diffraction pattern in which a main peak appears in at least one of them. From these diffraction results, the Ti oxide layer is composed of a material called a Magneli phase. it is clear that those represented by Ti n O 2n-1.
[0013]
BEST MODE FOR CARRYING OUT THE INVENTION
Next, the coated cermet tool of the present invention will be specifically described with reference to examples.
As raw material powders, WC powder, TiC powder both having an average particle size of 1 to 3 [mu] m, ZrC powder, VC powder, TaC powder, NbC powder, Cr 3 C 2 powder, TiN powder, prepared TaN powder and Co powder, Then, these raw material powders were blended into the blending composition shown in Table 1, further added with wax, ball-milled in acetone for 24 hours, dried under reduced pressure, and then pressed into a green compact of a predetermined shape at a pressure of 98 MPa. Then, this green compact is vacuum-sintered in a vacuum of 5 Pa at a predetermined temperature in the range of 1370 to 1470 ° C. for 1 hour, and after sintering, the cutting edge is honed with R: 0.07 mm. By processing, tool bases A to F made of a WC-based cemented carbide having a throw-away tip shape specified in ISO-CNMG120408 were manufactured, respectively.
[0014]
Further, as the raw material powder, both the average particle (TiC / TiN = 50/50 in mass ratio) TiCN having a diameter of 0.5~2μm powder, Mo 2 C powder, ZrC powder, NbC powder, TaC powder, WC powder , Co powder, and Ni powder are prepared, and these raw material powders are blended in the blending composition shown in Table 2, wet-mixed in a ball mill for 24 hours, dried, and pressed into a green compact at a pressure of 98 MPa. The green compact was sintered in a nitrogen atmosphere of 1.3 kPa at a temperature of 1540 ° C. for 1 hour, and after sintering, the cutting edge was subjected to a honing process of R: 0.07 mm to obtain an ISO. Tool bases a to f made of TiCN-based cermet having a chip shape of standard CNMG120412 were formed.
[0015]
Then, on the surfaces of the tool bases A to F and the tool bases a to f, a conventional chemical vapor deposition apparatus was used, and Table 3 (l-TiCN in Table 3 is a vertically long sheet described in JP-A-6-8010). It shows the conditions for forming a TiCN layer having a growth crystal structure, and the other conditions show the conditions for forming a normal granular crystal structure.) A compound layer is formed by vapor deposition as a lower layer of the hard coating layer, and then a κ-type or θ-type Al 2 O 3 layer is formed by vapor deposition under the same conditions as shown in Table 3, and the layer is formed in an Ar atmosphere at a temperature of: A heat transformation treatment is performed at a temperature of 1050 ° C. for a predetermined time within a range of 2 to 10 hours to transform the κ-type or θ-type crystal structure into an α-type. Table 5 also shows the distribution of the heated transformation α-type Al 2 O 3 layer. By forming the Ti oxide layer as the upper layer of the hard coating layer with the target layer thickness shown in FIG. Inventive coated cermet tools 1 to 12 were manufactured respectively.
For the purpose of comparison, as shown in Table 6, except that the upper layer of the hard coating layer was a vapor-deposited α-type Al 2 O 3 layer having an average layer thickness also shown in Table 6, and the surface layer was not formed. Manufactured the conventional coated cermet tools 1 to 12 under the same conditions.
[0016]
Further, X-ray diffraction was performed for the purpose of observing the difference between the heat-transformed α-type Al 2 O 3 layer and the vapor-deposited α-type Al 2 O 3 layer constituting the hard coating layer of the coated cermet tool of the present invention and the conventional coated cermet tool. It was measured.
In the measurement of these X-ray diffractions, a single crystal WC having diffraction peaks only on the (001) plane and the (002) plane on the X-ray diffraction chart was used as a substrate sample, and the surface of the substrate sample was coated with the coated cermet of the present invention. Heat-transformed α-type Al 2 O 3 layers having a target layer thickness of 15 μm, 10 μm, and 5 μm for tools 3, 7, and 11, and the same target layer thickness for conventional coated cermet tools 3, 7, and 11 also having a target layer thickness of 15 μm, 10 μm, Under the same conditions as the formation conditions of the deposited α-type Al 2 O 3 layer of 5 μm and 5 μm, respectively, and the heat-transformed α-type Al 2 O 3 layer and the deposited α-type Al 2 O 3 layer having the target layer thicknesses of 15 μm, 10 μm and 5 μm, respectively. Are directly formed to produce coating samples A to C of the present invention and conventional coating samples a to c. X-ray diffraction of the above-mentioned heat-transformed α-type Al 2 O 3 layer and vapor-deposited α-type Al 2 O 3 layer of these coated samples By measuring Carried out was. The measurement results are shown in FIGS.
FIGS. 1 to 3 show X-ray diffraction charts of the heat-transformed α-type Al 2 O 3 layers of coating samples A to C of the present invention, and X-ray diffraction charts of vapor-deposited α-type Al 2 O 3 layers of conventional coating samples a to c. 4 to 6, the heating-transformed α-type Al 2 O 3 layer shows clear diffraction peaks on the (006) plane and the (018) plane, whereas the vapor-deposited α-type Al 2 It is clear that the (006) plane and the (018) plane have no diffraction peak in the O 3 layer.
Further, a heat-transformed α-type Al 2 O 3 layer and a vapor-deposited α-type Al 2 O 3 layer having target layer thicknesses of 15 μm, 10 μm, and 5 μm, respectively, are directly formed on the surface of the substrate sample composed of the single crystal WC. For each of the heat-transformed α-type Al 2 O 3 layer and the vapor-deposited α-type Al 2 O 3 layer of the coated samples A to C of the present invention and the conventionally coated samples a to c, Electron beam backscatter diffraction (EBSD) of the crystal plane was performed using a thermal field emission scanning electron microscope (manufactured by JEOL Ltd.) and an azimuthal diffractometer (manufactured by Texem Laboratories, Inc.). In each of the heat-transformed α-type Al 2 O 3 layers, the crystal orientation map shows a dark red color tone, which is due to the hexagonal (0001) plane (hexagonal parallel plane), which is the crystal structure of Al 2 O 3. wherein the Al 2 O 3 layer surface (substrate trial It indicates that the oriented parallel to very strong relative to the surface), whereas said at deposition α-type Al 2 O 3 layer is either green or blue crystal orientation map, appear more yellow and pink and various shades This indicates that there is no specific orientation in the crystal plane constituting the hexagonal crystal.
[0017]
Further, with respect to the coated cermet tools 1 to 12 of the present invention and the conventional coated cermet tools 1 to 12 obtained as a result, the constituent layers of the hard coating layer were observed using a scanning electron microscope (observing the longitudinal section of the layers). As a result, the former consisted of a Ti compound layer, a heat-transformed α-type Al 2 O 3 layer in which cracks generated by heat transformation were dispersed and distributed in the layer, and a Ti oxide layer. It was confirmed that the layer consisted of a mold Al 2 O 3 layer.
Further, the surface layer of the coated cermet tools 1 to 12 of the present invention was measured for the oxygen content ratio (X value) at the center in the thickness direction using an Auger spectrometer, and the target values shown in Table 4 were obtained. And showed substantially the same value.
In addition, when the thicknesses of the constituent layers of the hard coating layer of these coated cermet tools were measured using a scanning electron microscope (also in the longitudinal section), the average layer thickness was substantially the same as the target layer thickness. (Average value of five-point measurements).
[0018]
Next, the above coated cermet tools 1 to 6 of the present invention and the conventional coated cermet tools 1 to 6 in a state where each of the above various coated cermet tools was screwed to the tip of a tool steel tool with a fixing jig, ,
Work material: Round bar with four vertical grooves at equal intervals in the length direction of JIS / SUS304,
Cutting speed: 400m / min,
Cut: 1.0 mm,
Feed: 0.15 mm / rev,
Cutting time: 3 minutes,
Dry high-speed intermittent cutting test of stainless steel under the conditions of
Work material: JIS S15C lengthwise round bar
Cutting speed: 450m / min,
Cut: 1.5 mm,
Feed: 0.2 mm / rev,
Cutting time: 3 minutes,
A dry high-speed interrupted cutting test of mild steel was performed under the following conditions.
[0019]
Further, for the coated cermet tools 7 to 12 of the present invention and the conventional coated cermet tools 7 to 12,
Work material: Round bar with four vertical grooves at equal intervals in the length direction of JIS / SUS304,
Cutting speed: 400m / min,
Cut: 0.5mm,
Feed: 0.15 mm / rev,
Cutting time: 3 minutes,
Dry high-speed intermittent cutting test of stainless steel under the conditions of
Work material: JIS S15C lengthwise round bar
Cutting speed: 450m / min,
Cut: 1.0 mm,
Feed: 0.15 mm / rev,
Cutting time: 3 minutes,
A dry high-speed intermittent cutting test was performed on mild steel under the following conditions, and the flank wear width of the cutting edge was measured in each cutting test. Table 7 shows the measurement results.
[0020]
[Table 1]
Figure 2004181555
[0021]
[Table 2]
Figure 2004181555
[0022]
[Table 3]
Figure 2004181555
[0023]
[Table 4]
Figure 2004181555
[0024]
[Table 5]
Figure 2004181555
[0025]
[Table 6]
Figure 2004181555
[0026]
[Table 7]
Figure 2004181555
[0027]
【The invention's effect】
From the results shown in Tables 5 to 7, the coated cermet tools 1 to 12 of the present invention were excellent due to the heat transformation generated cracks dispersed and distributed in the heat transformation α-type Al 2 O 3 layer constituting the upper layer of the hard coating layer. The effect of thermal shock absorption and excellent surface lubricity on the chips of the Ti oxide layer on the surface layer makes it possible to cut even high-speed interrupted cutting of stainless steel and mild steel with extremely high thermal shock and high heat generation. While the occurrence of chipping of the blade is remarkably suppressed and excellent wear resistance is exhibited, the conventional coated cermet tools 1 to 12 in which the upper layer of the hard coating layer is formed of a vapor-deposited α-type Al 2 O 3 layer have a high speed. In intermittent cutting, the vapor deposited α-type Al 2 O 3 layer cannot withstand severe thermal shock, the work material is extremely viscous, such as stainless steel or mild steel, and cutting chips are easily welded to the cutting surface. Phase with being wood I, chipping occurs in the cutting edge, it is clear that lead to a relatively short time service life.
As described above, the coated cermet tool of the present invention can be used not only for continuous cutting and interrupted cutting under normal conditions, but also for particularly difficult cutting materials with extremely high thermal shock and cutting conditions accompanied by high heat generation. It shows excellent chipping resistance even in high-speed interrupted cutting, and exhibits excellent cutting performance over a long period of time. It can be satisfied enough.
[Brief description of the drawings]
FIG. 1 is a diagram showing an X-ray diffraction chart of a heat-transformed α-type Al 2 O 3 layer (target layer thickness: 15 μm) constituting a hard coating layer of a coated cermet tool 3 of the present invention.
FIG. 2 is an X-ray diffraction chart of a heat-transformed α-type Al 2 O 3 layer (target layer thickness: 10 μm) constituting a hard coating layer of the coated cermet tool 7 of the present invention.
FIG. 3 is a view showing an X-ray diffraction chart of a heat-transformed α-type Al 2 O 3 layer (target layer thickness: 5 μm) constituting a hard coating layer of the coated cermet tool 11 of the present invention.
FIG. 4 is a diagram showing an X-ray diffraction chart of a vapor-deposited α-type Al 2 O 3 layer (target layer thickness: 15 μm) constituting a hard coating layer of the conventional coated cermet tool 3.
FIG. 5 is a diagram showing an X-ray diffraction chart of a vapor-deposited α-type Al 2 O 3 layer (target layer thickness: 10 μm) constituting a hard coating layer of the conventional coated cermet tool 7.
FIG. 6 is a diagram showing an X-ray diffraction chart of a vapor-deposited α-type Al 2 O 3 layer (target layer thickness: 5 μm) constituting a hard coating layer of the conventional coated cermet tool 11.

Claims (1)

炭化タングステン基超硬合金または炭窒化チタン基サーメットで構成された工具基体の表面に、
(a)下部層として、3〜20μmの平均層厚を有し、いずれも蒸着形成されたTiの炭化物層、窒化物層、炭窒化物層、炭酸化物層、および炭窒酸化物層のうちの1層または2層以上の積層からなるTi化合物層、
(b)上部層として、3〜15μmの平均層厚を有し、蒸着形成した状態でκ型またはθ型の結晶構造を有する酸化アルミニウムに加熱変態処理を施して結晶構造をα型結晶構造とし、かつ加熱変態生成クラックが分散分布した組織を有する加熱変態α型酸化アルミニウム層、
(c)表面層として、0.1〜5μmの平均層厚を有し、かつ、
組成式:TiOX
で表わした場合、厚さ方向中央部をオージェ分光分析装置で測定して、
X:Tiに対する原子比で1.2〜1.9、
を満足するTi酸化物層、
以上(a)〜(c)で構成された硬質被覆層を形成してなる、硬質被覆層がすぐれた耐熱衝撃性および表面潤滑性を有する表面被覆サーメット製切削工具。
On the surface of a tool substrate composed of tungsten carbide-based cemented carbide or titanium carbonitride-based cermet,
(A) As a lower layer, it has an average layer thickness of 3 to 20 μm, and is formed of a Ti carbide layer, a nitride layer, a carbonitride layer, a carbonate layer, and a carbonitride layer, all of which are formed by evaporation. A Ti compound layer composed of one or two or more layers of
(B) As an upper layer, aluminum oxide having an average layer thickness of 3 to 15 μm and having a κ-type or θ-type crystal structure in a vapor-deposited state is subjected to a heat transformation treatment to change the crystal structure to an α-type crystal structure. Heat transformation α-type aluminum oxide layer having a structure in which heat transformation generated cracks are dispersed and distributed,
(C) the surface layer has an average layer thickness of 0.1 to 5 μm, and
Composition formula: TiO x ,
When represented by, the center in the thickness direction is measured with an Auger spectrometer,
X: an atomic ratio to Ti of 1.2 to 1.9,
A Ti oxide layer that satisfies
A cutting tool made of a surface-coated cermet having a hard coating layer having excellent thermal shock resistance and surface lubricity, which is formed by forming the hard coating layer composed of (a) to (c) above.
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Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH03150364A (en) * 1989-06-16 1991-06-26 Sandvik Ab Coated article and coating thereof
JPH07112306A (en) * 1993-10-14 1995-05-02 Mitsubishi Materials Corp Surface coating cutting tool
JPH08277181A (en) * 1995-02-17 1996-10-22 Seco Tools Ab Insert of alumina-clad cemented carbide and its preparation
JPH10140353A (en) * 1996-11-14 1998-05-26 Mitsubishi Materials Corp Cutting, tool made of surface coated cemented carbide in which hard coating layer has excellent wear resistance
JP2001310203A (en) * 1999-08-12 2001-11-06 Mitsubishi Materials Corp Surface covered cemented carbide made cutting tool excellent in surface lubricity against chip

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH03150364A (en) * 1989-06-16 1991-06-26 Sandvik Ab Coated article and coating thereof
JPH07112306A (en) * 1993-10-14 1995-05-02 Mitsubishi Materials Corp Surface coating cutting tool
JPH08277181A (en) * 1995-02-17 1996-10-22 Seco Tools Ab Insert of alumina-clad cemented carbide and its preparation
JPH10140353A (en) * 1996-11-14 1998-05-26 Mitsubishi Materials Corp Cutting, tool made of surface coated cemented carbide in which hard coating layer has excellent wear resistance
JP2001310203A (en) * 1999-08-12 2001-11-06 Mitsubishi Materials Corp Surface covered cemented carbide made cutting tool excellent in surface lubricity against chip

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