JPS5952951B2 - cemented carbide - Google Patents
cemented carbideInfo
- Publication number
- JPS5952951B2 JPS5952951B2 JP12913781A JP12913781A JPS5952951B2 JP S5952951 B2 JPS5952951 B2 JP S5952951B2 JP 12913781 A JP12913781 A JP 12913781A JP 12913781 A JP12913781 A JP 12913781A JP S5952951 B2 JPS5952951 B2 JP S5952951B2
- Authority
- JP
- Japan
- Prior art keywords
- cemented carbide
- tin
- ratio
- tic
- tiw
- 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
Links
- 229910045601 alloy Inorganic materials 0.000 claims description 33
- 239000000956 alloy Substances 0.000 claims description 33
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 claims description 14
- 239000006104 solid solution Substances 0.000 claims description 14
- 239000011230 binding agent Substances 0.000 claims description 6
- 239000002184 metal Substances 0.000 claims description 5
- 229910052751 metal Inorganic materials 0.000 claims description 5
- 150000004767 nitrides Chemical class 0.000 claims description 4
- 150000001247 metal acetylides Chemical class 0.000 claims description 3
- 229910052742 iron Inorganic materials 0.000 claims description 2
- 229910052721 tungsten Inorganic materials 0.000 claims description 2
- 229910052758 niobium Inorganic materials 0.000 claims 2
- 229910052715 tantalum Inorganic materials 0.000 claims 2
- 238000005520 cutting process Methods 0.000 description 17
- 239000000463 material Substances 0.000 description 7
- 229910000831 Steel Inorganic materials 0.000 description 5
- 239000010959 steel Substances 0.000 description 5
- 230000000052 comparative effect Effects 0.000 description 4
- 239000000843 powder Substances 0.000 description 4
- 239000000047 product Substances 0.000 description 4
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 3
- 238000005336 cracking Methods 0.000 description 3
- 238000005245 sintering Methods 0.000 description 3
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 2
- 239000000919 ceramic Substances 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 238000003801 milling Methods 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 239000012188 paraffin wax Substances 0.000 description 2
- 239000002994 raw material Substances 0.000 description 2
- 229910000531 Co alloy Inorganic materials 0.000 description 1
- 229910009043 WC-Co Inorganic materials 0.000 description 1
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 238000005219 brazing Methods 0.000 description 1
- 238000005256 carbonitriding Methods 0.000 description 1
- 239000011195 cermet Substances 0.000 description 1
- 239000011247 coating layer Substances 0.000 description 1
- 239000013065 commercial product Substances 0.000 description 1
- 239000002131 composite material Substances 0.000 description 1
- 229910052593 corundum Inorganic materials 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- 239000010730 cutting oil Substances 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 239000010410 layer Substances 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 239000012299 nitrogen atmosphere Substances 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000010935 stainless steel Substances 0.000 description 1
- 229910001220 stainless steel Inorganic materials 0.000 description 1
- 238000004227 thermal cracking Methods 0.000 description 1
- 229910001845 yogo sapphire Inorganic materials 0.000 description 1
Description
【発明の詳細な説明】
本発明は、切削用、高靭性で耐亀裂損傷性、耐塑性変形
性に優れた大型サイドカッター、ホブ用途用の超硬合金
に関するものである。DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a cemented carbide for use in cutting, large side cutters, and hobs having high toughness, excellent crack damage resistance, and plastic deformation resistance.
WC基焼結合金は、TiC基焼結合金(以下サーメット
と記す)、A1□03基焼結合金(以下セラミックと記
す)、TiC,TiN、 T1CN、 AI□03等の
硬質被覆層をWC基焼結合金の表面に施した表面被覆合
金(以下コーテッド合金と記す)に比し、機械的強度、
耐熱疲労性等に優れるため、サーメット、セラミック、
コーテッド合金では使用に耐え得ない分野で広く使用さ
れている。WC-based sintered alloys are TiC-based sintered alloys (hereinafter referred to as cermets), A1□03-based sintered alloys (hereinafter referred to as ceramics), TiC, TiN, T1CN, AI□03, etc., with a hard coating layer on the WC base. Compared to surface-coated alloys applied to the surface of sintered alloys (hereinafter referred to as coated alloys), mechanical strength,
Cermet, ceramic,
It is widely used in fields where coated alloys cannot withstand use.
特に大型サイドカッター、ホブ等大きな衝撃力が働き、
かつ熱変動が工具刃先にががる鋼転削加工用分野では、
大いにその特徴を発揮している。In particular, large side cutters and hobs are subject to large impact forces,
In the field of steel milling where thermal fluctuations cause damage to the tool cutting edge,
It shows its characteristics to a great extent.
しかしながら、最近これらの分野においても、作業条件
の高能率化が進み、さらに工具寿命を改善させる要求が
高まりつ・ある。However, recently, even in these fields, working conditions have become more efficient, and there is an increasing demand for further improvement in tool life.
本発明は、これらの要求を満たすべく熱疲労性、衝撃靭
性を著しく改善した大型サイドカッター、ホブ、重切削
カッター等の鋼転削加工用に特に好適なWC基焼結合金
に関するものである。The present invention relates to a WC-based sintered alloy that has significantly improved thermal fatigue properties and impact toughness in order to meet these demands and is particularly suitable for steel milling such as large side cutters, hobs, and heavy cutting cutters.
本発明による超硬合金の特徴は、複合炭窒化物を含むB
l型固溶体とWC相からなる硬質相をFe族結合金属で
構成されたWC基焼結合金において、高速切削時の熱疲
労特性、衝撃靭性、耐摩耗性を最大限発揮できるべく、
これらの構成の組合わせの最適化を図ったことにある。The cemented carbide according to the present invention is characterized by B containing composite carbonitrides.
In order to maximize the thermal fatigue properties, impact toughness, and wear resistance during high-speed cutting in a WC-based sintered alloy in which the hard phase consisting of an L-type solid solution and a WC phase is composed of a Fe-group bonded metal,
The aim is to optimize the combination of these configurations.
硬質相中のWCは、機械的強度が大きく、熱伝導率が大
きい特徴を持っているが、高温下での鉄との反応に対す
る安定性や、耐酸化性等の特性が劣るため、これらの特
性にすぐれたTiCと組み合わせることにより、切削時
の耐摩耗特性を改善することは良く知られているところ
である。WC in the hard phase has the characteristics of high mechanical strength and high thermal conductivity, but these properties have poor stability against reactions with iron at high temperatures and oxidation resistance. It is well known that wear resistance during cutting can be improved by combining TiC with excellent properties.
一方、TiCは機械的強度が小さく、熱伝導率も低いた
め、添加量の増大により切削靭性を低下させる傾向にあ
ることも知られている。On the other hand, since TiC has low mechanical strength and low thermal conductivity, it is also known that increasing the amount added tends to reduce cutting toughness.
さらに、TiN/TiC比率で0.1〜0.60の範囲
にあるNを含有することにより、高靭性、高衝撃靭性の
超硬合金を得ることが出来るのも知られている。Furthermore, it is known that a cemented carbide with high toughness and high impact toughness can be obtained by containing N in a TiN/TiC ratio of 0.1 to 0.60.
発明者らは、さらにこれら焼結超硬合金について研究を
続けた結果、鋼の高速断続切削に特に優れた性能を示す
超硬合金を発明するに至った。The inventors further continued research on these sintered cemented carbide alloys, and as a result, they came up with a cemented carbide that exhibits particularly excellent performance in high-speed interrupted cutting of steel.
特に、被削材である鋼の硬度がブリネル硬さH8で20
0以上と硬くなった時、本発明合金は特開昭55−91
953で示された合金の性能を大幅に上回る。In particular, the hardness of the steel that is the work material is 20 on the Brinell hardness H8.
When the alloy becomes hard to 0 or more, the alloy of the present invention is
This significantly exceeds the performance of the alloy shown in No. 953.
すなわち、WCとBl型固溶体からなる硬質相とCoを
主体とするFe族金属からなる結合相で構成された超硬
合金において、硬質相の成分の内で、Ti、 wの炭化
物、窒化物、炭窒化物の部分が、TiC十TiN/Ti
C十TiN + WC比率に換算し、容積比率で0.4
0〜0.80の範囲にあり、Bl型固溶体がTiN/T
iC+ TiN比率、または(TiW) N/(TiW
) C十(TiW) N比率に換算し、重量比率で0.
1〜0.60の範囲にあるNを含有し、Coを主体とす
る結合相が最終合金全体の7〜20%の容積比率を占め
る超硬合金が、従来の超硬合金に比べ、高速切削時にお
ける耐摩耗性、靭性、耐熱亀裂性能で優れ、サイドカッ
ター、ホブ用途用等に最適であることがわかった。That is, in a cemented carbide composed of a hard phase consisting of WC and a Bl type solid solution and a binder phase consisting of an Fe group metal mainly composed of Co, among the components of the hard phase, Ti, w carbides, nitrides, The carbonitride part is TiC+TiN/Ti
Converting to C1TiN + WC ratio, the volume ratio is 0.4
It is in the range of 0 to 0.80, and the Bl type solid solution is TiN/T.
iC+ TiN ratio, or (TiW) N/(TiW
) C10 (TiW) Converted to N ratio, weight ratio is 0.
Cemented carbide containing N in the range of 1 to 0.60 and having a Co-based binder phase that accounts for 7 to 20% of the total volume of the final alloy has a higher cutting speed than conventional cemented carbide. It was found to have excellent wear resistance, toughness, and heat cracking resistance, making it ideal for side cutters, hobs, etc.
以下限定理由について述べる。The reasons for this limitation will be explained below.
硬質相の成分の内でTi、 Wの炭化物、窒化物、炭窒
化物の部分がTiC+ TiN/TiC+ TiN +
WC比率に換算し、容積比率で0.40以下では耐摩耗
特にHB200以上の高硬度鋼を切削する際の耐摩耗性
において不十分であり、0.8以上では強度不足による
チッピングが発生し易く、工具寿命が短い。Among the components of the hard phase, the carbides, nitrides, and carbonitrides of Ti and W are TiC+ TiN/TiC+ TiN +
In terms of WC ratio, if the volume ratio is less than 0.40, the wear resistance is insufficient, especially when cutting high hardness steel with HB200 or more, and if it is more than 0.8, chipping is likely to occur due to lack of strength. , short tool life.
次にBl型固溶体について述べる。Next, the Bl type solid solution will be described.
TiN/TiC+ TiN比率、または(TiW) N
/(TiW) C+ (TiW) N比率に換算し、重
量比率で0.1以下で耐熱亀裂性や靭性に劣る。TiN/TiC+ TiN ratio or (TiW) N
/(TiW) C+ (TiW) N When the weight ratio is 0.1 or less, the heat cracking resistance and toughness are poor.
すなわち、0.1以下では合金中のBl型固溶体結晶の
大きさが大きく成長してしまい、性能劣化の原因となる
。That is, if it is less than 0.1, the size of the Bl-type solid solution crystals in the alloy will grow large, causing performance deterioration.
逆に言えばNを加えることにより、Bl型固溶体の焼結
時における粒成長が大幅に抑制され、このことが本用途
において高性能を与える。Conversely, by adding N, grain growth during sintering of the Bl-type solid solution is significantly suppressed, which provides high performance in this application.
たパシ、0.6以上では焼結性を阻害し、耐摩耗性、靭
性とも不十分となる。If the hardness exceeds 0.6, sinterability will be inhibited and both wear resistance and toughness will be insufficient.
本発明の超硬合金中のB1型固溶体硬質相の平均粒径が
2μ以下で特に耐熱亀裂性に優れる。When the average grain size of the B1 type solid solution hard phase in the cemented carbide of the present invention is 2 μm or less, the heat cracking resistance is particularly excellent.
なお、本発明の超硬合金の強度を維持するためには、C
Oを主体とする結合金属が7容積%以下では靭性向で不
十分であり、20容積%以上では耐摩耗性が悪くなるの
で好ましくない。Note that in order to maintain the strength of the cemented carbide of the present invention, C
If the amount of the bonding metal mainly composed of O is less than 7% by volume, the toughness will be insufficient, and if it is more than 20% by volume, the wear resistance will deteriorate, which is not preferable.
なお、本発明の超硬合金部材中のB1型固溶体中に酸素
を含有していても本発明の効果は変らない。Note that even if oxygen is contained in the B1 type solid solution in the cemented carbide member of the present invention, the effects of the present invention do not change.
また、WCについては(MoW)Cに置換しても本発明
の効果は変らない。Further, even if WC is replaced with (MoW)C, the effects of the present invention do not change.
さらに、本発明合金の表面にTiC,T1CN。Furthermore, TiC and T1CN are added to the surface of the alloy of the present invention.
TiN、Al2O3,HfCなどの硬質相を1層もしく
は多層に被覆した被覆超硬工具の母材として有効なこと
は言うまでもない。Needless to say, it is effective as a base material for coated carbide tools coated with a hard phase such as TiN, Al2O3, HfC, etc. in one layer or in multiple layers.
以下実施例にて説明する。This will be explained below using examples.
〔実施例 1〕
第1表に示す組成で源料を配合し、さらにプレス助剤と
してのパラフィンを1.5重量%加え、18−8ステン
レス製の容器とWC−Co焼結合金製のボールを用い、
アセトン中で120時間のボールミル混合を行った。[Example 1] The raw materials were blended according to the composition shown in Table 1, 1.5% by weight of paraffin was added as a press aid, and a container made of 18-8 stainless steel and a ball made of WC-Co sintered alloy were mixed. using
Ball mill mixing was performed in acetone for 120 hours.
これを乾燥後1.5t/cm□の圧力にて切削用チップ
をプレス成型した後、真空中で420℃に保持し、パラ
フィンを除去した後、窒表分圧50Torrの減圧窒素
雰囲気下で焼結温度1425℃に1時間保持し焼結体を
得た。After drying, a cutting tip was press-molded at a pressure of 1.5 t/cm□, and then kept in a vacuum at 420°C to remove paraffin, and then baked in a reduced pressure nitrogen atmosphere with a nitrogen surface partial pressure of 50 Torr. A sintered body was obtained by maintaining the sintering temperature at 1425° C. for 1 hour.
表中に合金特性、切削試験の結果を併せ記した。Alloy properties and cutting test results are also listed in the table.
本発明品は比較合金に比べ優れていることがわかった。It was found that the product of the present invention is superior to comparative alloys.
〔実施例 2〕
TiO2粉末とWO3粉末を用いて、炭窒化反応により
(TiW) (CN)粉末を作った。[Example 2] (TiW) (CN) powder was produced by carbonitriding reaction using TiO2 powder and WO3 powder.
この粉末と残部は実施例1で使用した原料を用い、第3
表のとおりの配合組成の合金を作成した。For this powder and the remainder, the raw materials used in Example 1 were used, and the third
An alloy with the composition shown in the table was prepared.
ボールミル混合時間は100時間、焼結温度は1380
℃である。Ball mill mixing time is 100 hours, sintering temperature is 1380
It is ℃.
これらの合金特性を第3表に示す。The properties of these alloys are shown in Table 3.
これらの試作合金と市販t7)WC−TiC−TaC−
Co合金系のJIS分類PIO,P2O,P30相当材
質の合金を選択し第4表に示す結果が得られた。These prototype alloys and commercially available t7) WC-TiC-TaC-
The results shown in Table 4 were obtained by selecting Co alloy-based alloys with materials corresponding to JIS classifications PIO, P2O, and P30.
〔実施例 3〕
実施例1で作成した合金Fを用い、大型サイドカッター
によるテストを行った。[Example 3] Using alloy F prepared in Example 1, a test was conducted using a large side cutter.
比較材種としては市販被覆材種のP30相当品並びに比
較合金Bを用いた。As comparative materials, a commercially available coated material equivalent to P30 and comparative alloy B were used.
被削材: 550C(HB260)
使用工具:大型サイドカッタ−25インチ切削条件:切
削速度176m/分
切込み 2〜5mm
送り 0.316mm/刃
本発明品は6時間の寿命に対し、市販品P30は2時間
、比較合金Bは4時間の寿命であった。Work material: 550C (HB260) Tool used: Large side cutter - 25 inches Cutting conditions: Cutting speed 176 m/min Depth of cut 2-5 mm Feed 0.316 mm/blade The invented product has a lifespan of 6 hours, while the commercial product P30 has a lifespan of 6 hours. Comparative Alloy B had a life of 4 hours.
〔実施例 4〕
実施例2で作成した合金Kを用い、ロー付はホブ(モジ
ュール1.25、圧力角、切刃溝数14)を製作しテス
トした。[Example 4] Using alloy K prepared in Example 2, a brazing hob (module 1.25, pressure angle, number of cutting grooves 14) was manufactured and tested.
切削条件
被削材: 545C(HB280)
切削速度:280m/分
送り:5mm/回転
切削油:不水溶性油
本発明は120m切削可能に対し、市販超硬合金P20
は5m、P2Oは10mでいずれも熱亀裂によりチッピ
ングを生じた。Cutting conditions Workpiece material: 545C (HB280) Cutting speed: 280 m/min Feed: 5 mm/rotation Cutting oil: Water-insoluble oil The present invention can cut 120 m, whereas commercially available cemented carbide P20
Chipping occurred due to thermal cracking at 5 m and P2O at 10 m.
〔実施例 5〕
実施例4のホブを公告のCVD、並びにPVD法により
コーティングして切削テストしたところ、本発明品にの
コーテイング品は寿命150mと向上したが、市販P2
0のコーテイング品は1mも切削できなかった。[Example 5] When the hob of Example 4 was coated by the publicly announced CVD and PVD methods and a cutting test was conducted, the coated product of the present invention had an improved lifespan of 150 m, but the commercially available P2
0 coated product could not be cut even 1m.
Claims (1)
体からなる硬質相とCoを主体とするFe金属からなる
結合相で構成された超硬合金において、硬質相の成分を
Ti、 wの炭化物、窒化物として分解して(TiC+
TiN) / (TiC+WC十TiN)比率に換算し
、容積比率で0.40〜0.80の範囲にあり、Bl型
固溶体がTiN / (TiC十TiN )比率または
(TiW) N/ (TiW) C+ (TiW) N
比率に換算し、重量比率で0.1〜0.6の範囲にある
Nを含有し、WCは合金全体で20〜80重量%、CO
を主体とする結合相が最終合金体の7〜20容積%の比
率を占めることを特徴とする超硬合金。 2、特許請求の範囲第1項記載の超硬合金において、最
終焼結体に存在するBl型固溶体硬質相が平均粒径2μ
以下である超硬合金。 3 WCとTi、 wおよびTa、Nbから選ばれた
1種または2種からなる炭窒化物のBl型固溶体からな
る硬質相とCoを主体とするFe金属からなる結合相で
構成された超硬合金において、硬質相の成分をTi、
Wの炭化物、窒化物として分解して(TiC+TiN)
/ (TiC十WC+TiN)比率に換算し、容積比率
で0.40〜0.80の範囲にあり、Bl型固溶体がT
iN / (TiC+ TiN )比率または(TiW
) N/ (TiW) C十(TiW) N比率に換算
し、重量比率でO01〜0.6の範囲にあるNを含有し
、WCは合金全体で20〜80重量%、Ta、Nbより
選ばれた1種または2種を合金全体で2〜20重量%、
COを主体とする結合相が最終合金体の7〜20容積%
の比率を占めることを特徴とする超硬合金。 4 特許請求の範囲第3項記載の超硬合金において、最
終焼結体に存在するBl型固溶体硬質相が平均粒径2μ
以下である超硬合金。[Claims] I A cemented carbide composed of a hard phase consisting of a Bl-type solid solution of carbonitrides consisting of WC, Ti, and W, and a binder phase consisting of an Fe metal mainly composed of Co, in which the components of the hard phase are is decomposed into Ti, w carbides and nitrides (TiC+
Converted to TiN) / (TiC + WC + TiN) ratio, the volume ratio is in the range of 0.40 to 0.80, and the BL type solid solution has a TiN / (TiC + TiN) ratio or (TiW) N / (TiW) C + (TiW)N
Contains N in the range of 0.1 to 0.6 in terms of weight ratio, WC is 20 to 80% by weight in the entire alloy, and CO
A cemented carbide characterized in that a binder phase mainly composed of occupies 7 to 20% by volume of the final alloy body. 2. In the cemented carbide according to claim 1, the Bl type solid solution hard phase present in the final sintered body has an average grain size of 2 μm.
Cemented carbide which is below. 3 Carbide composed of a hard phase consisting of a Bl-type solid solution of carbonitride consisting of WC and one or two selected from Ti, w, Ta, and Nb, and a binder phase consisting of Fe metal mainly composed of Co. In the alloy, the components of the hard phase are Ti,
Decomposes W as carbide and nitride (TiC+TiN)
/ (TiC + WC + TiN) The volume ratio is in the range of 0.40 to 0.80, and the Bl type solid solution is T
iN/(TiC+TiN) ratio or (TiW
) N/ (TiW) C (TiW) Contains N in the weight ratio range of O01 to 0.6 in terms of N ratio, WC is 20 to 80% by weight in the entire alloy, selected from Ta and Nb. 2 to 20% by weight of one or two of the above in the entire alloy,
CO-based binder phase accounts for 7-20% by volume of the final alloy body
Cemented carbide is characterized by having a ratio of . 4 In the cemented carbide according to claim 3, the Bl type solid solution hard phase present in the final sintered body has an average grain size of 2 μm.
Cemented carbide which is below.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP12913781A JPS5952951B2 (en) | 1981-08-18 | 1981-08-18 | cemented carbide |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP12913781A JPS5952951B2 (en) | 1981-08-18 | 1981-08-18 | cemented carbide |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS5831057A JPS5831057A (en) | 1983-02-23 |
| JPS5952951B2 true JPS5952951B2 (en) | 1984-12-22 |
Family
ID=15002026
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP12913781A Expired JPS5952951B2 (en) | 1981-08-18 | 1981-08-18 | cemented carbide |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS5952951B2 (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US8859115B2 (en) | 2003-06-13 | 2014-10-14 | Mitsubishi Materials Corporation | Cemented carbide material for surface coated gear cutting tool and surface coated gear cutting tool |
Families Citing this family (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS60258446A (en) * | 1984-06-04 | 1985-12-20 | Toshiba Tungaloy Co Ltd | Sintered alloy |
| JPS6433589A (en) * | 1987-07-30 | 1989-02-03 | Kenwood Corp | Display device |
| JPH0711051B2 (en) * | 1988-09-07 | 1995-02-08 | 東芝タンガロイ株式会社 | Cemented carbide and coated cemented carbide formed by forming a coating on the surface of the alloy |
-
1981
- 1981-08-18 JP JP12913781A patent/JPS5952951B2/en not_active Expired
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US8859115B2 (en) | 2003-06-13 | 2014-10-14 | Mitsubishi Materials Corporation | Cemented carbide material for surface coated gear cutting tool and surface coated gear cutting tool |
Also Published As
| Publication number | Publication date |
|---|---|
| JPS5831057A (en) | 1983-02-23 |
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