JP3291775B2 - Surface coated cutting tool - Google Patents
Surface coated cutting toolInfo
- Publication number
- JP3291775B2 JP3291775B2 JP20711092A JP20711092A JP3291775B2 JP 3291775 B2 JP3291775 B2 JP 3291775B2 JP 20711092 A JP20711092 A JP 20711092A JP 20711092 A JP20711092 A JP 20711092A JP 3291775 B2 JP3291775 B2 JP 3291775B2
- Authority
- JP
- Japan
- Prior art keywords
- layer
- cutting tool
- aluminum oxide
- coated cutting
- coated
- 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
Links
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- Cutting Tools, Boring Holders, And Turrets (AREA)
- Chemical Vapour Deposition (AREA)
- Other Surface Treatments For Metallic Materials (AREA)
Description
【0001】[0001]
【産業上の利用分野】この発明は、超硬合金基体または
サーメット基体の表面に化学蒸着法により形成された、
チタンの炭化物、窒化物、炭窒化物、炭酸化物および炭
窒酸化物のうち1種の単層または2種以上の複層(以
下、チタン化合物層と総称する)並びに少なくとも1層
の酸化アルミニウム層からなる複合硬質層を形成してな
る耐摩耗性および耐欠損性に優れた表面被覆切削工具に
関するものである。The present invention relates to a cemented carbide or cermet substrate formed by a chemical vapor deposition method on a surface of the substrate.
One kind or two or more kinds of titanium carbide, nitride, carbonitride, carbonate and carbonitride, and at least one aluminum oxide layer The present invention relates to a surface-coated cutting tool having excellent wear resistance and fracture resistance formed by forming a composite hard layer composed of:
【0002】[0002]
【従来の技術】従来、超硬合金基体またはサーメット基
体の表面に、化学蒸着法によりチタン化合物層および少
なくとも1層の酸化アルミニウム層からなる複合硬質層
を被覆してなる表面被覆切削工具は、鋼などの連続切削
や断続切削に用いられていることは良く知られている。2. Description of the Related Art Conventionally, a surface-coated cutting tool obtained by coating a surface of a cemented carbide substrate or a cermet substrate with a composite hard layer composed of a titanium compound layer and at least one aluminum oxide layer by a chemical vapor deposition method is known as steel. It is well known that it is used for continuous cutting and interrupted cutting.
【0003】前記酸化アルミニウム層は、前記チタン化
合物層よりも耐摩耗性に優れているが、密着性および靭
性に劣るために、超硬合金基体またはサーメット基体の
表面に化学蒸着法により先ずチタン化合物層を被覆し、
このチタン化合物層の上に化学蒸着法により酸化アルミ
ニウム層を被覆し、形成された複合硬質層の耐摩耗性お
よび靭性を付与して耐欠損性を向上させている。[0003] The aluminum oxide layer is superior in wear resistance to the titanium compound layer, but is inferior in adhesion and toughness. Therefore, a titanium compound layer is first formed on the surface of a cemented carbide substrate or a cermet substrate by a chemical vapor deposition method. Coating layers,
An aluminum oxide layer is coated on the titanium compound layer by a chemical vapor deposition method to impart abrasion resistance and toughness of the formed composite hard layer to improve fracture resistance.
【0004】前記複合硬質層における酸化アルミニウム
層を化学蒸着法により形成する方法として、通常の反応
ガスに0.01〜1.0Vol%の硫化水素ガスを含む
反応ガスを用いることにより酸化アルミニウム層の成長
速度を向上させる方法が知られている。この方法による
と、酸化アルミニウム層の成長速度が向上するところか
らその他の被覆層および基体を高温に長時間さらすこと
なく組織変化を防止することができ、したがって、従来
の被覆切削工具よりも優れた性能を有する表面被覆切削
工具が得られるといわれている(例えば、特公昭62−
3234号公報参照)。As a method of forming the aluminum oxide layer in the composite hard layer by a chemical vapor deposition method, a reaction gas containing 0.01 to 1.0% by volume of hydrogen sulfide gas is used as a normal reaction gas to form the aluminum oxide layer. Methods for improving the growth rate are known. According to this method, since the growth rate of the aluminum oxide layer is improved, the structure change can be prevented without exposing other coating layers and the substrate to high temperatures for a long time, and therefore, it is superior to the conventional coated cutting tools. It is said that a surface-coated cutting tool having high performance can be obtained (for example,
No. 3234).
【0005】[0005]
【発明が解決しようとする課題】しかし、近年、切削工
程の省力化および短縮化に対する要求は強く、これに伴
ない、より一段と苛酷な条件下での高送りおよび高切込
みなどの高速連続重切削や断続切削が強いられる傾向に
あるが、前記従来の硫化水素ガス:0.01〜0.3V
ol%を含む反応ガスを用い化学蒸着して得られた酸化
アルミニウム層を含む複合硬質層が被覆された切削工具
は、これら苛酷な条件下では、被覆層の耐摩耗性および
耐欠損性が不十分であり、比較的短時間の使用寿命しか
示さないのが現状である。However, in recent years, there has been a strong demand for labor saving and shortening of the cutting process, and accompanying this, high speed continuous heavy cutting such as high feed and high cutting under more severe conditions has been accompanied. However, the conventional hydrogen sulfide gas: 0.01 to 0.3 V
Under such severe conditions, a cutting tool coated with a composite hard layer containing an aluminum oxide layer obtained by chemical vapor deposition using a reactive gas containing ol% does not have abrasion resistance and fracture resistance of the coating layer. At present, it is sufficient and shows only a relatively short service life.
【0006】[0006]
【課題を解決するための手段】そこで本発明者らは、さ
らに一層耐摩耗性および耐欠損性に優れた酸化アルミニ
ウム層を含む複合硬質層が被覆された表面被覆切削工具
を開発すべく研究を行っていたところ、 (1) 前記従来のWC基超硬合金製切削工具またはT
iCN基サーメット製切削工具基体表面に硫化水素ガ
ス:0.01〜1.0Vol%を含む反応ガスを用い化
学蒸着法により形成された酸化アルミニウム層は、α型
結晶を有しかつX線回折における(104)面のピーク
強度:I(104)に対する(030)面のピーク強
度:I(030)の比が、I(030)/I(104)
≦1であるような酸化アルミニウムで構成されており、
かかる結晶構造の酸化アルミニウム層は、十分な耐摩耗
性および耐欠損性を示さない、Accordingly, the present inventors have conducted research to develop a surface-coated cutting tool coated with a composite hard layer including an aluminum oxide layer which is more excellent in wear resistance and fracture resistance. (1) The conventional WC-based cemented carbide cutting tool or T
An aluminum oxide layer formed on the surface of a cutting tool substrate made of an iCN-based cermet by a chemical vapor deposition method using a reaction gas containing hydrogen sulfide gas: 0.01 to 1.0% by volume has an α-type crystal and is subjected to X-ray diffraction. The ratio of the peak intensity of the (030) plane: I (030) to the peak intensity of the (104) plane: I (104) is I (030) / I (104).
≦ 1 made of aluminum oxide,
The aluminum oxide layer having such a crystal structure does not exhibit sufficient wear resistance and fracture resistance.
【0007】(2) その理由として、(104)面に
配向性を示すα型結晶酸化アルミニウムは(030)面
に配向性を示すα型結晶酸化アルミニウムに比べて結晶
学的に見て密度が低く、かかる密度の低い(104)面
に配向性を示すα型結晶酸化アルミニウムが(030)
面に配向性を示すα型結晶酸化アルミニウムよりも多く
含まれる従来のα型結晶酸化アルミニウム層は、十分な
耐摩耗性および耐欠損性を示さないものと考えられる、(2) The reason is that α-type crystal aluminum oxide having orientation on the (104) plane has a crystallographically higher density than α-type crystal aluminum oxide having orientation on the (030) plane. Low-density α-type crystal aluminum oxide exhibiting orientation on the (104) plane having a low density is (030)
The conventional α-type crystal aluminum oxide layer containing more than the α-type crystal aluminum oxide showing orientation on the surface is considered to not show sufficient wear resistance and chipping resistance,
【0008】(3) したがって、前記酸化アルミニウ
ム層を、X線回折における(030)面のピーク強度I
(030)をX線回折における(104)面のピーク強
度I(104)よりも大である、すなわち、I(03
0)>I(104)であるようなα型結晶の酸化アルミ
ニウムで構成すると、耐摩耗性および耐欠損性が一層向
上し、この酸化アルミニウム層を含む複合硬質層を被覆
した表面被覆切削工具は、使用寿命が一層向上する、 (4) 前記I(030)>I(104)であるような
α型結晶の酸化アルミニウム層は、通常の化学蒸着法に
おいて、通常の化学蒸着反応ガス中に硫化水素ガス:
0.01〜2.0Vol%および二酸化硫黄ガス:0.
01〜1.0Vol%を添加した反応ガスを用いること
により形成される、 などの知見を得たのである。(3) Therefore, the peak intensity I of the (030) plane in the X-ray diffraction is determined by
(030) is larger than the peak intensity I (104) of the (104) plane in X-ray diffraction, that is, I (03)
0)> I (104), when composed of aluminum oxide of α-type crystal, the wear resistance and fracture resistance are further improved, and the surface-coated cutting tool coated with the composite hard layer containing this aluminum oxide layer is (4) The aluminum oxide layer of the α-type crystal in which I (030)> I (104) is sulfided in a normal chemical vapor deposition reaction gas by a normal chemical vapor deposition method. Hydrogen gas:
0.01-2.0 Vol% and sulfur dioxide gas:
It was found that the reaction gas was formed by using a reaction gas to which 01 to 1.0% by volume was added.
【0009】この発明は、かかる知見にもとずいてなさ
れたものであって、基体表面に、チタン化合物層(Ti
C、TiN、TiCN、TiCO、TiCNOなどのう
ちの単層または2種以上の複層からなる硬質被覆層)お
よび少なくとも1層の酸化アルミニウム層からなる複合
硬質層を被覆してなる切削工具において、前記酸化アル
ミニウム層は、α型結晶を有し、かつX線回折における
(104)面のピーク強度:I(104)に対する(0
30)面のピーク強度:I(030)の比が、I(03
0)/I(104)>1であるような酸化アルミニウム
で構成されている表面被覆切削工具に特徴を有するもの
である。The present invention has been made on the basis of this finding, and a titanium compound layer (Ti
C, TiN, TiCN, TiCO, TiCNO, etc. in a cutting tool coated with a single hard layer or a hard coating layer formed of two or more layers and a composite hard layer formed of at least one aluminum oxide layer. The aluminum oxide layer has an α-type crystal and has a peak intensity of (104) plane in X-ray diffraction: (0) with respect to I (104).
30) The ratio of the plane peak intensity: I (030) is I (03).
0) / I (104)> 1 is characterized by a surface-coated cutting tool made of aluminum oxide.
【0010】この発明の表面被覆切削工具を製造するに
は、通常の表面を研削処理したサーメット製切削工具
(WC基超硬合金製切削工具なども含む)を基体とし、
この基体表面に、通常の化学蒸着法により少なくとも1
層のチタン化合物層を形成し、そのチタン化合物層の上
に、さらに少なくとも1層のこの発明の酸化アルミニウ
ム層を形成することにより作製される。前記酸化アルミ
ニウム層は、必ずしも最外層である必要はなく、酸化ア
ルミニウム層の上にさらに少なくとも1層のチタン化合
物層を被覆しても良い。In order to manufacture the surface-coated cutting tool of the present invention, a cermet cutting tool (including a WC-based cemented carbide cutting tool or the like) having a normal surface ground is used as a substrate.
The surface of the substrate is coated with at least one
It is produced by forming a titanium compound layer, and further forming at least one aluminum oxide layer of the present invention on the titanium compound layer. The aluminum oxide layer is not necessarily the outermost layer, and at least one titanium compound layer may be further coated on the aluminum oxide layer.
【0011】前記この発明のI(030)/I(10
4)>1であるような酸化アルミニウム層を形成するに
は、通常の酸化アルミニウム層を形成するための化学蒸
着反応ガス中にH2 Sガス:0.01〜2.0Vol%
およびSO2 ガス:0.01〜1.0Vol%を添加し
た反応ガスを用いることにより形成され、H2 Sガスお
よびSO2 ガスとは、 2H2 S+SO2 =3S+2H2 O となるように反応してSと水を生成し、さらに、生成し
た水は塩化アルミニウムと反応し、 H2 O+2AlCl=Al2 O3 +6HCl となり、このときI(030)/I(104)>1であ
るようなAl2 O3 が生成されるものと考えられる。In the present invention, I (030) / I (10
4) In order to form an aluminum oxide layer satisfying> 1, H 2 S gas: 0.01 to 2.0 Vol% in a chemical vapor deposition reaction gas for forming a normal aluminum oxide layer.
And SO 2 gas: formed by using a reaction gas to which 0.01 to 1.0 Vol% is added, and reacts with H 2 S gas and SO 2 gas so that 2H 2 S + SO 2 = 3S + 2H 2 O. To produce S and water, and the generated water reacts with aluminum chloride to form H 2 O + 2AlCl = Al 2 O 3 + 6HCl, where Al 2 is such that I (030) / I (104)> 1. It is believed that O 3 is produced.
【0012】[0012]
【実施例】つぎに、この発明の表面被覆切削工具の製造
法を実施例により具体的に説明する。通常の粉末冶金法
により製造した72%WC−8%TiC−10%TaC
−10%Coからなる成分組成(ISO規格P30相
当)を有しかつISO規格のSNMG432に定めた形
状の切削工具を用意した。Next, a method for manufacturing a surface-coated cutting tool according to the present invention will be specifically described with reference to examples. 72% WC-8% TiC-10% TaC manufactured by ordinary powder metallurgy
A cutting tool having a component composition of -10% Co (corresponding to ISO standard P30) and having a shape defined by ISO standard SNMG432 was prepared.
【0013】実施例1 この切削工具を通常の化学蒸着装置に装入し、温度:1
000℃、圧力:50torr、反応ガス組成:3%TiC
l4 −9%CH4 −88%H2 、の条件で厚さ:3μm
のTiC層を形成し、その上に、温度:1000℃、圧
力:100torr、反応ガス組成:4%TiCl4 −2%
CO−2%CH4 −22%N2 −70%H2 、の条件で
厚さ:0.5μmのTiCNO層を形成し、さらにその
上に、温度:1000℃、圧力:50torr、反応ガス組
成:6%AlCl3 −10%CO2 −6%HCl−2%
H2 S−1%SO2 −75%H2 、の条件で厚さ:4μ
mのAl2 O3 層を形成し、本発明被覆切削工具1を作
製した。Example 1 This cutting tool was charged into a conventional chemical vapor deposition apparatus, and the temperature was set at 1: 1.
000 ° C, pressure: 50 torr, reaction gas composition: 3% TiC
Thickness: 3 μm under the condition of l 4 -9% CH 4 -88% H 2 .
A TiC layer having a temperature of 1000 ° C., a pressure of 100 torr, and a reaction gas composition of 4% TiCl 4 -2%
A TiCNO layer having a thickness of 0.5 μm is formed under the conditions of CO-2% CH 4 -22% N 2 -70% H 2 , and further, a temperature: 1000 ° C., a pressure: 50 torr, and a reaction gas composition : 6% AlCl 3 -10% CO 2 -6% HCl-2%
H 2 S-1% SO 2 -75% H 2, conditions with a thickness of: 4 [mu]
An Al 2 O 3 layer of m was formed to produce a coated cutting tool 1 of the present invention.
【0014】従来例1 実施例1と同じ条件でTiC層およびTiCNO層を形
成した後、温度:1000℃、圧力:50torr、反応ガ
ス組成:6%AlCl3 −10%CO2 −6%HCl−
1.0%H2 S−77%H2 、の条件で厚さ:4μmの
Al2 O3 層を形成し、従来被覆切削工具1を作製し
た。Conventional Example 1 After forming a TiC layer and a TiCNO layer under the same conditions as in Example 1, temperature: 1000 ° C., pressure: 50 torr, reaction gas composition: 6% AlCl 3 -10% CO 2 -6% HCl—
An Al 2 O 3 layer having a thickness of 4 μm was formed under the conditions of 1.0% H 2 S-77% H 2 , and a conventional coated cutting tool 1 was produced.
【0015】実施例2 前記切削工具を通常の化学蒸着装置に装入し、温度:1
000℃、圧力:50torr、反応ガス組成:3%TiC
l4 −6%CH4 −26%N2 −65%H2 、の条件で
厚さ:4μmのTiCN層を形成し、その上に、温度:
1000℃、圧力:50torr、反応ガス組成:3%Ti
Cl4 −9%CH4 −88%H2 、の条件で厚さ:1μ
mのTiC層を形成し、その上に、温度:1000℃、
圧力:100torr、反応ガス組成:4%TiCl4 −2
%CO−2%CH4 −22%N2 −70%H2 、の条件
で厚さ:0.5μmのTiCNO層を形成し、さらにそ
の上に、温度:1000℃、圧力:50torr、反応ガス
組成:6%AlCl3 −10%CO2 −6%HCl−
0.6%H2 S−0.3%SO2 −77.1%H2 、の
条件で厚さ:3μmのAl2 O3 層を形成し、本発明被
覆切削工具2を作製した。Example 2 The above cutting tool was charged into a conventional chemical vapor deposition apparatus, and the temperature was 1: 1.
000 ° C, pressure: 50 torr, reaction gas composition: 3% TiC
A TiCN layer having a thickness of 4 μm is formed under the conditions of l 4 -6% CH 4 -26% N 2 -65% H 2 , and a temperature:
1000 ° C., pressure: 50 torr, reaction gas composition: 3% Ti
Cl 4 -9% CH 4 -88% H 2 , thickness: 1 μm
m of a TiC layer, and a temperature of 1000 ° C.
Pressure: 100 torr, reaction gas composition: 4% TiCl 4 -2
% CO-2% CH 4 -22% N 2 -70% H 2 , a TiCNO layer having a thickness of 0.5 μm is formed, and a temperature of 1000 ° C., a pressure of 50 torr and a reaction gas are further formed thereon. Composition: 6% AlCl 3 -10% CO 2 -6% HCl—
An Al 2 O 3 layer having a thickness of 3 μm was formed under the conditions of 0.6% H 2 S−0.3% SO 2 −77.1% H 2 , thereby producing a coated cutting tool 2 of the present invention.
【0016】従来例2 実施例2と同じ条件でTiCN層、TiC層およびTi
CNO層を形成した後、温度:1000℃、圧力:50
torr、反応ガス組成:6%AlCl3 −10%CO2 −
6%HCl−0.3%H2 S−77.7%H2 、の条件
で厚さ:3μmのAl2 O3 層を形成し、従来被覆切削
工具2を作製した。Conventional Example 2 A TiCN layer, a TiC layer and a Ti
After forming the CNO layer, temperature: 1000 ° C., pressure: 50
torr, reaction gas composition: 6% AlCl 3 -10% CO 2 −
An Al 2 O 3 layer having a thickness of 3 μm was formed under the conditions of 6% HCl-0.3% H 2 S-77.7% H 2 , and a conventional coated cutting tool 2 was produced.
【0017】実施例3 この切削工具を通常の化学蒸着装置に装入し、温度:1
000℃、圧力:50torr、反応ガス組成:3%TiC
l4 −9%CH4 −88%H2 、の条件で厚さ:1μm
のTiC層を形成し、その上に、温度:1000℃、圧
力:100torr、反応ガス組成:4%TiCl4 −6%
CO−90%H2 、の条件で厚さ:0.5μmのTiC
O層を形成し、さらにその上に、温度:1000℃、圧
力:50torr、反応ガス組成:6%AlCl3 −10%
CO2 −6%HCl−1%H2 S−0.5%SO2 −7
6.5%H2 、の条件で厚さ:3μmのAl2 O3 層を
形成し、本発明被覆切削工具3を作製した。Example 3 This cutting tool was charged in a conventional chemical vapor deposition apparatus, and the temperature was 1: 1.
000 ° C, pressure: 50 torr, reaction gas composition: 3% TiC
l 4 -9% CH 4 -88% H 2, conditions with a thickness of: 1 [mu] m
A TiC layer having a temperature of 1000 ° C., a pressure of 100 torr, and a reaction gas composition of 4% TiCl 4 -6%
0.5 μm TiC under the condition of CO-90% H 2 .
An O layer is formed, and a temperature: 1000 ° C., a pressure: 50 torr, and a reaction gas composition: 6% AlCl 3 -10%
CO 2 -6% HCl-1% H 2 S-0.5% SO 2 -7
An Al 2 O 3 layer having a thickness of 3 μm was formed under the condition of 6.5% H 2 , thereby producing a coated cutting tool 3 of the present invention.
【0018】実施例3と同じ条件でTiC層およびTi
CO層を形成した後、温度:1000℃、圧力:50to
rr、反応ガス組成:6%AlCl3 −10%CO2 −6
%HCl−0.5%H2 S−77.5%H2 、の条件で
厚さ:3μmのAl2 O3 層を形成し、従来被覆切削工
具3を作製した。Under the same conditions as in Example 3, the TiC layer and Ti
After forming the CO layer, temperature: 1000 ° C., pressure: 50 to
rr, reaction gas composition: 6% AlCl 3 -10% CO 2 -6
An Al 2 O 3 layer having a thickness of 3 μm was formed under the conditions of% HCl-0.5% H 2 S-77.5% H 2 , and a conventional coated cutting tool 3 was produced.
【0019】実施例4〜6 実施例1〜3で作製した本発明被覆切削工具1〜3のA
l2 O3 層の表面に、さらに温度:1000℃、圧力:
200torr、反応ガス組成:2%TiCl4 −38%N
2 −60%H2 、の条件で厚さ:1μmのTiN層を形
成し、本発明被覆切削工具4〜6を作製した。Examples 4-6 A of the coated cutting tools 1-3 of the present invention produced in Examples 1-3.
on the surface of the l 2 O 3 layer, further temperature: 1000 ° C., pressure:
200 torr, reaction gas composition: 2% TiCl 4 -38% N
A TiN layer having a thickness of 1 μm was formed under the conditions of 2 to 60% H 2 , thereby producing coated cutting tools 4 to 6 of the present invention.
【0020】従来例1〜3で作製した従来被覆切削工具
1〜3のAl2 O3 層の表面に、さらに温度:1000
℃、圧力:200torr、反応ガス組成:2%TiCl4
−38%N2 −60%H2 、の条件で厚さ:1μmのT
iN層を形成し、従来被覆切削工具4〜6を作製した。On the surface of the Al 2 O 3 layer of each of the conventional coated cutting tools 1 to 3 produced in Conventional Examples 1 to 3, a temperature of 1000 was further added.
° C, pressure: 200 torr, reaction gas composition: 2% TiCl 4
-38% N 2 -60% H 2 , thickness: 1 μm T
An iN layer was formed, and conventionally coated cutting tools 4 to 6 were produced.
【0021】これら本発明被覆切削工具1〜6および従
来被覆切削工具1〜6について、X線回折を行ない、
(104)面のピーク強度:I(104)に対する(0
30)面のピーク強度:I(030)の比=I(03
0)/I(104)を求め、それらの値を表1に示し
た。X-ray diffraction was performed on these coated cutting tools 1 to 6 of the present invention and conventional coated cutting tools 1 to 6,
(104) plane peak intensity: (0) with respect to I (104)
30) plane peak intensity: ratio of I (030) = I (03)
0) / I (104) was determined, and their values are shown in Table 1.
【0022】得られた本発明被覆切削工具1〜6および
従来被覆切削工具1〜6について、 被削材 :SNCM439(硬さ:HB 230) 切削速度:180m/min 送 り:0.3mm/rev 切込み :2.0mm 切削時間:30min 冷却油 :なし の条件で鋼の連続切削試験を行ない、切刃の逃げ面摩耗
幅を測定し、これらの結果も表1に示し、[0022] The present invention coated cutting tool 6 and the conventional coated cutting tools 1 to 6 were obtained, Workpiece: SNCM439 (Hardness: H B 230) Cutting speed: 180 m / min feed Ri: 0.3 mm / rev Depth of cut: 2.0 mm Cutting time: 30 min Cooling oil: None A continuous cutting test of steel was performed, and the flank wear width of the cutting edge was measured. These results are also shown in Table 1.
【0022】さらに、本発明被覆切削工具1〜6および
従来被覆切削工具1〜6について、 被削材 :SNCM439(硬さ:HB 230)角材 切削速度:100m/min 送 り:0.236mm/rev 切込み :3.0mm 切削時間:30min 冷却油 :なし の条件で鋼の断続切削試験を行ない、工具刃先が欠損に
至までの時間を測定し、これらの結果も表1に示した。Furthermore, the present invention coated cutting the tool 6 and the conventional coated cutting tools 1 to 6, Workpiece: SNCM439 (Hardness: H B 230) square bar Cutting speed: 100 m / min feed Ri: 0.236mm / rev Depth of cut: 3.0 mm Cutting time: 30 min Cooling oil: None An intermittent cutting test was performed on the steel, and the time until the cutting edge of the tool reached fracture was measured. The results are also shown in Table 1.
【0023】[0023]
【表1】 [Table 1]
【0024】[0024]
【発明の効果】表1に示された結果から明らかなよう
に、本発明被覆切削工具1〜6のAl2O3 層のI(0
30)/I(104)の値はいずれも1より大である
が、従来被覆切削工具1〜6のAl2 O3 層のI(03
0)/I(104)の値はいずれも1以下であり、基体
に被覆されるAl2 O3 層のI(030)/I(10
4)の値が1より大きな本発明被覆切削工具1〜6は従
来被覆切削工具1〜6に比べていずれも連続切削試験を
行なった際の逃げ面摩耗幅が小さくかつ断続切削試験に
よる欠損に至までの時間が長いことがわかる。As is evident from the results shown in Table 1, the I (0) of the Al 2 O 3 layer of the coated cutting tools 1 to 6 of the present invention.
The values of 30) / I (104) are all greater than 1, but I (03) of the Al 2 O 3 layer of the conventional coated cutting tools 1-6.
0) / I (104) is 1 or less, and I (030) / I (10) of the Al 2 O 3 layer coated on the substrate.
The coated cutting tools 1 to 6 of the present invention in which the value of 4) is larger than 1 have a smaller flank wear width when a continuous cutting test is performed than the conventional coated cutting tools 1 to 6 and are less likely to suffer defects caused by an intermittent cutting test. It can be seen that the time until the solstice is long.
【0025】したがって、この発明の表面被覆切削工具
は、従来の表面被覆切削工具よりも一層優れた切削性能
を有しており、この発明の表面被覆切削工具を用いるこ
とにより切削工具交換回数などを減らすことができ、産
業の発展に大いに貢献しうるものである。Therefore, the surface-coated cutting tool of the present invention has a cutting performance which is more excellent than that of the conventional surface-coated cutting tool. It can be reduced and can greatly contribute to the development of industry.
───────────────────────────────────────────────────── フロントページの続き (58)調査した分野(Int.Cl.7,DB名) B23B 27/14 B23P 15/28 C23C 16/30 - 16/40 C23C 28/04 ──────────────────────────────────────────────────の Continued on the front page (58) Field surveyed (Int. Cl. 7 , DB name) B23B 27/14 B23P 15/28 C23C 16/30-16/40 C23C 28/04
Claims (1)
炭窒化物、炭酸化物および炭窒酸化物のうち1種の単層
または2種以上の複層、並びに少なくとも1層の酸化ア
ルミニウム層からなる複合硬質層を被覆してなる切削工
具において、 前記酸化アルミニウム層は、α型結晶を有し、かつX線
回折による(104)面のピーク強度:I(104)に
対する(030)面のピーク強度:I(030)の比
が、I(030)/I(104)>1であるような酸化
アルミニウムで構成されていることを特徴とする表面被
覆切削工具。Claims: 1. A titanium carbide, nitride,
A cutting tool coated with a single hard layer of carbonitrides, carbon oxides and carbonitrides, or a composite hard layer comprising at least one aluminum oxide layer; The aluminum layer has an α-type crystal and the ratio of the peak intensity of the (030) plane: I (030) to the peak intensity of the (104) plane: I (104) by X-ray diffraction is I (030) / A surface-coated cutting tool comprising an aluminum oxide such that I (104)> 1.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP20711092A JP3291775B2 (en) | 1992-07-10 | 1992-07-10 | Surface coated cutting tool |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP20711092A JP3291775B2 (en) | 1992-07-10 | 1992-07-10 | Surface coated cutting tool |
Publications (2)
Publication Number | Publication Date |
---|---|
JPH0631503A JPH0631503A (en) | 1994-02-08 |
JP3291775B2 true JP3291775B2 (en) | 2002-06-10 |
Family
ID=16534367
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP20711092A Expired - Lifetime JP3291775B2 (en) | 1992-07-10 | 1992-07-10 | Surface coated cutting tool |
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JP (1) | JP3291775B2 (en) |
Cited By (1)
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---|---|---|---|---|
WO2013031952A1 (en) | 2011-08-31 | 2013-03-07 | 三菱マテリアル株式会社 | Surface-coated cutting tool |
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JP2004284003A (en) | 2003-02-28 | 2004-10-14 | Mitsubishi Materials Corp | Surface-coated cermet cutting tool exhibiting excellent chipping resistance in hard coated layer |
JP2005131730A (en) * | 2003-10-30 | 2005-05-26 | Mitsubishi Materials Corp | Surface-coated cermet cutting tool with hard coating layer having superior chipping resistance |
US7273665B2 (en) | 2003-12-22 | 2007-09-25 | Mitsubishi Materials Corporation | Surface-coated cermet cutting tool with hard coating layer having excellent chipping resistance |
JP4512989B2 (en) * | 2003-12-26 | 2010-07-28 | 三菱マテリアル株式会社 | Surface coated cermet cutting tool with excellent chipping resistance with hard coating layer |
JP4529578B2 (en) * | 2004-08-05 | 2010-08-25 | 三菱マテリアル株式会社 | Surface coated cermet cutting tool whose hard coating layer exhibits excellent chipping resistance in high speed heavy cutting |
JP4518260B2 (en) | 2005-01-21 | 2010-08-04 | 三菱マテリアル株式会社 | Surface-coated cermet cutting tool whose hard coating layer exhibits excellent chipping resistance in high-speed intermittent cutting |
JP4716251B2 (en) * | 2005-03-24 | 2011-07-06 | 三菱マテリアル株式会社 | A surface-coated cermet cutting tool that exhibits excellent chipping resistance with a hard coating layer in high-speed intermittent cutting of high-hardness steel |
JP4716252B2 (en) * | 2005-05-24 | 2011-07-06 | 三菱マテリアル株式会社 | Surface-coated cermet cutting tool with excellent chipping resistance thanks to thick α-type aluminum oxide layer |
JP4716253B2 (en) * | 2005-05-24 | 2011-07-06 | 三菱マテリアル株式会社 | Surface-coated cermet cutting tool with excellent chipping resistance thanks to thick α-type aluminum oxide layer |
EP1788124B1 (en) | 2005-11-18 | 2008-09-24 | Mitsubishi Materials Corporation | Surface coated cutting tool made of cermet having property-modified alpha type Al2O3 layer of hard coating layer |
-
1992
- 1992-07-10 JP JP20711092A patent/JP3291775B2/en not_active Expired - Lifetime
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2013031952A1 (en) | 2011-08-31 | 2013-03-07 | 三菱マテリアル株式会社 | Surface-coated cutting tool |
US9636748B2 (en) | 2011-08-31 | 2017-05-02 | Mitsubishi Materials Corporation | Surface-coated cutting tool |
Also Published As
Publication number | Publication date |
---|---|
JPH0631503A (en) | 1994-02-08 |
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