JPS58181845A - Tough cermet - Google Patents
Tough cermetInfo
- Publication number
- JPS58181845A JPS58181845A JP6457082A JP6457082A JPS58181845A JP S58181845 A JPS58181845 A JP S58181845A JP 6457082 A JP6457082 A JP 6457082A JP 6457082 A JP6457082 A JP 6457082A JP S58181845 A JPS58181845 A JP S58181845A
- Authority
- JP
- Japan
- Prior art keywords
- cermet
- metal
- carbide
- group
- cutting
- 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.)
- Granted
Links
- 239000011195 cermet Substances 0.000 title claims abstract description 24
- 229910052751 metal Inorganic materials 0.000 claims abstract description 40
- 239000002184 metal Substances 0.000 claims abstract description 40
- 150000004767 nitrides Chemical class 0.000 claims abstract description 16
- -1 TiN Chemical class 0.000 claims abstract description 6
- 229910052721 tungsten Inorganic materials 0.000 claims abstract description 5
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 claims abstract description 4
- 239000012535 impurity Substances 0.000 claims abstract description 4
- MTPVUVINMAGMJL-UHFFFAOYSA-N trimethyl(1,1,2,2,2-pentafluoroethyl)silane Chemical compound C[Si](C)(C)C(F)(F)C(F)(F)F MTPVUVINMAGMJL-UHFFFAOYSA-N 0.000 claims description 18
- CAVCGVPGBKGDTG-UHFFFAOYSA-N alumanylidynemethyl(alumanylidynemethylalumanylidenemethylidene)alumane Chemical compound [Al]#C[Al]=C=[Al]C#[Al] CAVCGVPGBKGDTG-UHFFFAOYSA-N 0.000 claims description 8
- 239000000126 substance Substances 0.000 claims description 8
- 150000002739 metals Chemical class 0.000 claims description 7
- 150000001247 metal acetylides Chemical class 0.000 claims description 6
- 230000000737 periodic effect Effects 0.000 claims description 3
- 238000005520 cutting process Methods 0.000 abstract description 34
- 238000005245 sintering Methods 0.000 abstract description 15
- 239000000203 mixture Substances 0.000 abstract description 11
- 239000004033 plastic Substances 0.000 abstract description 6
- 229910052759 nickel Inorganic materials 0.000 abstract description 5
- 229910052804 chromium Inorganic materials 0.000 abstract description 3
- 229910052750 molybdenum Inorganic materials 0.000 abstract description 3
- CWYNVVGOOAEACU-UHFFFAOYSA-N Fe2+ Chemical compound [Fe+2] CWYNVVGOOAEACU-UHFFFAOYSA-N 0.000 abstract 2
- 229910016384 Al4C3 Inorganic materials 0.000 abstract 1
- 229910003178 Mo2C Inorganic materials 0.000 abstract 1
- 238000013329 compounding Methods 0.000 abstract 1
- 230000000052 comparative effect Effects 0.000 description 16
- NRTOMJZYCJJWKI-UHFFFAOYSA-N Titanium nitride Chemical compound [Ti]#N NRTOMJZYCJJWKI-UHFFFAOYSA-N 0.000 description 11
- 238000000034 method Methods 0.000 description 11
- 239000011230 binding agent Substances 0.000 description 8
- 239000000919 ceramic Substances 0.000 description 8
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 7
- 239000000956 alloy Substances 0.000 description 7
- 229910045601 alloy Inorganic materials 0.000 description 7
- 230000007423 decrease Effects 0.000 description 7
- 230000000694 effects Effects 0.000 description 7
- 239000000843 powder Substances 0.000 description 6
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical group [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 5
- 239000002994 raw material Substances 0.000 description 5
- 238000004519 manufacturing process Methods 0.000 description 4
- PMHQVHHXPFUNSP-UHFFFAOYSA-M copper(1+);methylsulfanylmethane;bromide Chemical compound Br[Cu].CSC PMHQVHHXPFUNSP-UHFFFAOYSA-M 0.000 description 3
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- ZOKXTWBITQBERF-UHFFFAOYSA-N Molybdenum Chemical compound [Mo] ZOKXTWBITQBERF-UHFFFAOYSA-N 0.000 description 2
- 239000011651 chromium Substances 0.000 description 2
- 230000007547 defect Effects 0.000 description 2
- 238000001035 drying Methods 0.000 description 2
- 229910052742 iron Inorganic materials 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 238000003801 milling Methods 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- 239000011733 molybdenum Substances 0.000 description 2
- 229910052757 nitrogen Inorganic materials 0.000 description 2
- WFKWXMTUELFFGS-UHFFFAOYSA-N tungsten Chemical compound [W] WFKWXMTUELFFGS-UHFFFAOYSA-N 0.000 description 2
- 239000010937 tungsten Substances 0.000 description 2
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 description 1
- 208000006558 Dental Calculus Diseases 0.000 description 1
- 229910026551 ZrC Inorganic materials 0.000 description 1
- OTCHGXYCWNXDOA-UHFFFAOYSA-N [C].[Zr] Chemical compound [C].[Zr] OTCHGXYCWNXDOA-UHFFFAOYSA-N 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 238000005266 casting Methods 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 229910017052 cobalt Inorganic materials 0.000 description 1
- 239000010941 cobalt Substances 0.000 description 1
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 description 1
- 239000002131 composite material Substances 0.000 description 1
- 230000029142 excretion Effects 0.000 description 1
- 239000002783 friction material Substances 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 230000002496 gastric effect Effects 0.000 description 1
- 229910052735 hafnium Inorganic materials 0.000 description 1
- 230000008595 infiltration Effects 0.000 description 1
- 238000001764 infiltration Methods 0.000 description 1
- 230000002401 inhibitory effect Effects 0.000 description 1
- 238000002347 injection Methods 0.000 description 1
- 239000007924 injection Substances 0.000 description 1
- 238000001746 injection moulding Methods 0.000 description 1
- 239000000314 lubricant Substances 0.000 description 1
- UNASZPQZIFZUSI-UHFFFAOYSA-N methylidyneniobium Chemical compound [Nb]#C UNASZPQZIFZUSI-UHFFFAOYSA-N 0.000 description 1
- 238000000465 moulding Methods 0.000 description 1
- 229910052758 niobium Inorganic materials 0.000 description 1
- 239000010955 niobium Substances 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 239000011505 plaster Substances 0.000 description 1
- 239000002002 slurry Substances 0.000 description 1
- 239000006104 solid solution Substances 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 239000010935 stainless steel Substances 0.000 description 1
- 229910001220 stainless steel Inorganic materials 0.000 description 1
- 238000006467 substitution reaction Methods 0.000 description 1
- 229910052715 tantalum Inorganic materials 0.000 description 1
- 229910052720 vanadium Inorganic materials 0.000 description 1
- 229910052726 zirconium Inorganic materials 0.000 description 1
Abstract
Description
【発明の詳細な説明】
本発明は靭性及び耐熱耐摩耗性に優れた切削工具用サー
メットに関する。DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a cermet for cutting tools that has excellent toughness and heat and wear resistance.
サーメットはセラミックと金属とからなる複合材料であ
り、セラミックの耐熱性、^硬度と金属の強度、靭性と
を併有するとされ、各種切削工具、摩擦材料、自己潤滑
材料、is材料等に広く応用されているものである。Cermet is a composite material consisting of ceramic and metal, and is said to have both the heat resistance and hardness of ceramic and the strength and toughness of metal, and is widely used in various cutting tools, friction materials, self-lubricating materials, IS materials, etc. This is what is being done.
特に切削工具としては従来、炭化チタンと金属ニッケル
との組み合わせ、炭化チタン及び窒化チタンと金属ニッ
ケルとの組み合わせを主体とした工具が使用されてきて
いる。特にセラミック成分として炭化チタンと窒化チタ
ンとの組み合わせを採用した場合炭化チタンのみと比較
して高温硬さ熱伝導率が改善されたものである。In particular, as cutting tools, tools mainly made of a combination of titanium carbide and metal nickel, or a combination of titanium carbide or titanium nitride and metal nickel have been used. In particular, when a combination of titanium carbide and titanium nitride is used as the ceramic component, high-temperature hardness and thermal conductivity are improved compared to titanium carbide alone.
しかし、上記セラミック成分として炭化チタンと窒化チ
タンを組み合わせると、窒化チタンが金属成分とのぬれ
が思いため靭性あるいは耐摩耗性が満足できる程の改善
がなされなかった。この問題点を解決するものとして、
炭化ジルコニウム、炭化タルタル、炭化ニオブ、タング
ステン、モリブデン、窒化アルミニウム等を炭化チタン
及び窒化チタンと組み合わせてセラミック成分とし、鉄
族金属を金属成分としてサーメットを成形したもの(特
許出願公開昭和54年第30209号ンが開発され、優
れた切削特性、機械的特性等を有することが知られてい
る。However, when titanium carbide and titanium nitride are combined as the ceramic components, the titanium nitride tends to wet with the metal components, so that the toughness or wear resistance cannot be improved to a satisfactory extent. As a solution to this problem,
A cermet formed by combining zirconium carbide, tartar carbide, niobium carbide, tungsten, molybdenum, aluminum nitride, etc. with titanium carbide and titanium nitride as a ceramic component, and using an iron group metal as a metal component (Patent Application Publication No. 30209, 1972) No. 2 was developed and is known to have excellent cutting characteristics, mechanical properties, etc.
しかしながら、上記のようにサーメットに窒化アルミニ
ウム等を配合したことにより切削特性、機械的特性が白
土したとはいえ、合金の製造工程における真空焼結の際
、窒化チタンが窒素を分解発生してボアや栄等の合金欠
陥が発生し強度が低下するという現瘉が生じていた。更
にこの現象は、 窒化チタンの配合により焼結温度を
上昇させる必要があることからも促進される形となった
。その上窒化チタン自体、鉄族金属とのぬれが悪いため
ボアが多く従って強度低下の原因となっており、窒化ア
ルミニウム等の配合で強化しても十分な強度が得にり<
、特に重切削や衝撃の大きいフライス切削、断続切削に
はほとんど使用されていない状態であり、高速切削に用
いた場合にも耐摩耗性、耐塑性変形性にも麺があった。However, although the cutting properties and mechanical properties were improved by adding aluminum nitride, etc. to the cermet as described above, during vacuum sintering in the manufacturing process of the alloy, titanium nitride decomposes nitrogen and generates bore holes. There was a problem in which alloy defects such as Sakae and Sakae occurred, resulting in a decrease in strength. Furthermore, this phenomenon was accelerated by the need to increase the sintering temperature due to the addition of titanium nitride. Furthermore, titanium nitride itself has poor wettability with iron group metals, so it has many bores, which causes a decrease in strength, and even if it is strengthened with aluminum nitride, sufficient strength cannot be obtained.
In particular, it is hardly used for heavy cutting, milling cutting with large impact, or interrupted cutting, and even when used for high-speed cutting, it has poor wear resistance and plastic deformation resistance.
本発明者らは上記の問題点を解決すべく鋺意研究の結束
、窒化チタン等の窒化物を配合した炭化チタン系サーメ
ットに更に炭化アルミニウムを配合することにより、従
来の欠点を解消できることを見い出し、本発明を完成し
た。In order to solve the above-mentioned problems, the present inventors conducted extensive research and discovered that the conventional drawbacks could be overcome by adding aluminum carbide to a titanium carbide cermet containing nitrides such as titanium nitride. , completed the invention.
即ち、本発明の要旨とするところは、次の成分(a )
元素周期律表の■a及びVa族金属窒化物から選ば
れた1種又は2種以上:5〜30重鋤%
(b) Via族金属及び該金属炭化物から選ばれた
1種又は2種以上=3ぐ4011a1%(C) 鉄族
金属から選ばれた1種又は21以上:2.85〜30重
鏝%
(d)1512化アルミニウム:0.15〜8重量%(
e) 炭化チタン及び不可避不純物:残部から成るこ
とを特徴とする強靭サーメットにある。That is, the gist of the present invention is that the following component (a)
■One or more selected from a and Va group metal nitrides of the Periodic Table of the Elements: 5 to 30% (b) One or more selected from Via group metals and their metal carbides =3g4011a1% (C) One or more selected from iron group metals: 2.85 to 30% by weight (d) Aluminum 1512: 0.15 to 8% by weight (
e) Titanium carbide and unavoidable impurities: The tough cermet is characterized by consisting of the remainder.
ここにおいて元素周期律表のIVa族とは元素記号で表
わすとT1、Zr及びHfから成る族、Va族とはV、
Nb及びTaから成る族、■a族とはCr 、MO及び
Wから成る族及び鉄族金属とはFe 、Co及びNiか
らなる族を意味する。Here, the IVa group of the periodic table of elements is a group consisting of T1, Zr, and Hf, and the Va group is a group consisting of V,
The group consisting of Nb and Ta, the group ①a means the group consisting of Cr, MO and W, and the iron group metal means the group consisting of Fe, Co and Ni.
本発明に使用される成分の内、IV a族金属の窒化物
としては、化学式Ti N、Zr N、Hf Nで表さ
れるもの、Va族金属の窒化物としては化学式VN、N
b N、Ta Nで表わされるもの、■aa族金属して
はクロム、モリブデン、タングステン、Vl a族金属
炭化物としては化学式Cr5C2、Cr7Ca、MQz
C,MOC,W2C,WCr表わされるもの、鉄族金属
としては鉄、コバルト、ニッケル、炭化アルミニウムと
しては化学式A立aCSぐ表わされるもの及び炭化チタ
ンとしては化学式TiCで表わされるものが本発明のサ
ーメット組成成分として適用可能である。Among the components used in the present invention, nitrides of IV group a metals are represented by the chemical formulas TiN, ZrN, and HfN, and nitrides of group Va metals are represented by chemical formulas VN, N
b N, Ta N, ■ AA group metals include chromium, molybdenum, tungsten, Vla group a metal carbides include chemical formulas Cr5C2, Cr7Ca, MQz
The cermets of the present invention include those represented by C, MOC, W2C, and WCr, iron group metals such as iron, cobalt, and nickel, aluminum carbide represented by the chemical formula A and aCS, and titanium carbide represented by the chemical formula TiC. Applicable as a composition component.
上記成分の内、IVa及びVa族金属窒化物は合金の粒
成長抑−1作用の他に耐クレータ摩耗性の改善作用があ
り、その含有量は5〜30%が好ましく、5%未満では
上記作用効果が薄れ、30%を越えると耐摩耗性が低下
する。Among the above components, IVa and Va group metal nitrides have the effect of inhibiting the grain growth of the alloy as well as improving the crater wear resistance, and their content is preferably 5 to 30%, and if it is less than 5%, the above The effect is weakened, and if it exceeds 30%, the wear resistance decreases.
又、■aa族金属びこれらの炭化物はセラミックの硬質
相と金属の結合相とのぬれ性を改善する効果があり、そ
の含有量は3〜40%が好ましく、3%未満では上記作
用効果が薄れ、40%を越えると炭化チタンの周辺にで
きる複炭窒化物の相が脆くなり合金の強度や耐酸化性が
低下する。更に相対的に炭化チタンの鏝が減少し耐摩耗
性が低下する。In addition, ■ AA group metals and their carbides have the effect of improving the wettability between the hard phase of the ceramic and the binder phase of the metal, and their content is preferably 3 to 40%, and if it is less than 3%, the above effects will be weakened. If it exceeds 40%, the double carbonitride phase formed around titanium carbide becomes brittle, reducing the strength and oxidation resistance of the alloy. Furthermore, the amount of titanium carbide is relatively reduced, resulting in a decrease in wear resistance.
又、鉄族金属は結合相としての効果を果し、その含有−
は2.85%〜30%が好ましく、2゜85%未満では
合金の強度が低下し、30%を越えると合金の硬度が低
下し、耐摩耗性が悪化する。In addition, iron group metals act as a binder phase, and their content -
is preferably 2.85% to 30%; if it is less than 2.85%, the strength of the alloy will decrease, and if it exceeds 30%, the hardness of the alloy will decrease and its wear resistance will deteriorate.
又、炭化アルミニウムは硬質相と結合相とのぬれ性を大
幅に向上させ、又、焼結温度を下げる効果があり、その
含有量は0.15〜8%が好ましく、0.15%未満で
は上記効果が十分でなく、8%を越えると強度や切削特
性が低下する。In addition, aluminum carbide significantly improves the wettability between the hard phase and the binder phase, and also has the effect of lowering the sintering temperature, so its content is preferably 0.15 to 8%, and less than 0.15%. The above effects are not sufficient, and if it exceeds 8%, the strength and cutting characteristics will deteriorate.
更に上述した成分に加えて硬質相としての炭化チタン及
び不可避不純物が残部を占め、これらの成分を主体に本
発明のサーメットが構成されているが、炭化チタンの一
部をIva及びVa族金属炭化物で置換すると硬質相と
結合相とのぬれ性を向上させるばかりでなく耐熱性をも
向上させることが可能である。その含有量は元の炭化チ
タンの薇の40%以下が好ましく、置換−が40%を越
えると上記の効果が薄れると共に、相対的に炭化チタン
の量も減少するので、炭化チタンの特性である耐摩耗性
が低下する。Furthermore, in addition to the above-mentioned components, titanium carbide as a hard phase and unavoidable impurities account for the remainder, and the cermet of the present invention is mainly composed of these components. When substituted with , it is possible to improve not only the wettability between the hard phase and the binder phase but also the heat resistance. The content is preferably 40% or less of the original titanium carbide, and if the substitution exceeds 40%, the above effects will be weakened and the amount of titanium carbide will also be relatively reduced, which is a characteristic of titanium carbide. Wear resistance decreases.
次にサーメット製造にあたって使用される各成分は、混
合及び成形の容易さから粉末状のものが用いられ、一般
にその粒径は10μ以下のものが用いられる。又、各成
分は単一でなく、炭化物と炭化物、炭化物と窒化物ある
いは窒化物と窒化物の固溶体の形で用いてもよい。Next, each component used in cermet production is in powder form for ease of mixing and molding, and generally has a particle size of 10 μm or less. Moreover, each component may not be used alone, but in the form of a solid solution of carbide and carbide, carbide and nitride, or nitride and nitride.
上記の原料を用いて成形されたサーメットを製造する方
法は、通常サーメット製造に採用されているい(つかの
方法を用途に応じて、適宜選択できる。例えば、セラミ
ック粉末と金II粉末とを混合し、湿式で混合したもの
は乾燥後に、冷間で金型を用い加圧して賦形し、次いで
焼結する冷間成形焼結法、溶媒と共に泥漿を作り石膏型
のような多孔質型に鋳込んで成形乾燥し、次いで焼結す
る鋳込み成形焼結法、セラミック粉末を予めバインダ及
び潤滑剤と共に混合し成形及び1次焼結して多孔質焼結
体を1M3!it、これに金属を溶浸させる溶浸法、金
属及びセラミック粉末をプラスチックバインダと共に混
合し射出成形後バインダをとばし焼結する射出成形焼結
法、その他焼結時に圧力を加えるホットプレス法、HI
P法、CAP法等の方法が採用可能である。これらの焼
結は一般に不活性又は還元性ガス中で1250〜1 L
、00℃、0.1〜3時間でなされる。The method for manufacturing a molded cermet using the above-mentioned raw materials is one that is normally adopted for manufacturing cermets. After drying, the wet mixture is pressurized and shaped using a cold mold, and then sintered, which is the cold forming sintering method. A slurry is created with a solvent and cast into a porous mold such as a plaster mold. In the casting sintering method, ceramic powder is mixed with a binder and lubricant in advance, molded and primary sintered to form a porous sintered body of 1M3!it, which is then sintered. Infiltration method in which metal and ceramic powders are mixed with a plastic binder and injection molded, the binder is blown off and sintered after injection molding, hot press method in which pressure is applied during sintering, and HI
Methods such as the P method and the CAP method can be adopted. These sinterings are generally carried out in an inert or reducing gas at 1250 to 1 L.
, 00°C for 0.1 to 3 hours.
以上詳述した如く上記各成分を用い焼結製造された本発
明のサーメットは窒化チタンを初めとする■aあるいは
va族金属の窒化物を含有する炭化チタン系サーメット
に炭化アルミニウムを配合したことにより、窒化物を含
む硬質相と結合相金属とのぬれ性が大幅に改善され、焼
結温度も窒化チタンを数%〜数十%添加した従来のサー
メットに比べて大幅に低下する。そのためボアが少なく
微細組織のサーメット焼結体が得られる。更に、本発明
のサーメットは機械的特性、・切削特性に優れ従来のサ
ーメット■具では使用が限定されていた重切削や衝撃の
大きいフライス切削、断続切削、切削時に応用の大きさ
や方向の変化する倣い切削に優れた特性を示し、又、耐
摩耗性、耐塑性変形性の著しい向上により、高速切削に
も十分な性能を発揮するものである。As detailed above, the cermet of the present invention manufactured by sintering using each of the above components is obtained by blending aluminum carbide into a titanium carbide-based cermet containing nitrides of Group A or Va metals, including titanium nitride. , the wettability between the hard phase containing nitride and the binder phase metal is significantly improved, and the sintering temperature is also significantly lower than that of conventional cermets containing titanium nitride in an amount of several percent to several tens of percent. Therefore, a cermet sintered body with a small bore and a fine structure can be obtained. Furthermore, the cermet of the present invention has excellent mechanical properties and cutting properties, making it suitable for heavy cutting, high-impact milling, interrupted cutting, and cutting in which the size and direction change. It exhibits excellent characteristics in profile cutting, and has sufficient performance in high-speed cutting due to significantly improved wear resistance and plastic deformation resistance.
次に本発明の実施例により具体的に説明する。Next, the present invention will be specifically explained using examples.
実施例1
切削工具用焼結合金原料として市販されて0る第1表の
原料粉末を使用し、これらの原料粉末をを第2表に示す
各試料No、成分組成に配合し、この配合物をステンレ
ス製ボールミルと超硬ボールとを用い湿式混合した。次
いでこの混合物を乾燥後、プレス圧2t/−で成形し、
輿空中温1i1300〜1350℃で1時間焼結を行っ
て得た切削工具用チップについて抗折力(TR8)と硬
度を測定した。その後、5NP432の寸法に研磨して
第3表に示す切削条件で切削試験を行った。Example 1 Using the raw material powders shown in Table 1 that are commercially available as raw materials for sintered alloys for cutting tools, these raw material powders were blended with each sample number and component composition shown in Table 2, and this mixture was prepared. were wet mixed using a stainless steel ball mill and carbide balls. Next, after drying this mixture, it was molded at a press pressure of 2t/-,
The transverse rupture strength (TR8) and hardness of the cutting tool chips obtained by sintering for 1 hour at an air temperature of 1i1300 to 1350°C were measured. Thereafter, it was polished to the dimensions of 5NP432 and a cutting test was conducted under the cutting conditions shown in Table 3.
得られた結果を各実施例の組成と共に第2表に併記した
。尚、比較例のサーメットも同方法で作成し同様な測定
を行い第2表に併記した。但し比較例の試料No、1−
10については焼結温度1350℃以下では焼結不可能
であったので、別に1420℃で焼結を行った。The obtained results are listed in Table 2 together with the composition of each example. Incidentally, a cermet of a comparative example was also prepared by the same method and measured in the same manner, and is also listed in Table 2. However, sample No. 1- of comparative example
As for Sample No. 10, it was impossible to sinter at a sintering temperature of 1350°C or lower, so sintering was performed separately at 1420°C.
以上の結果から、■a族金属炭化物としてWC及びMO
2Cの合計量が45%と(b)成分が40%を越えて大
壷に配合された比較例の試料1−8は、硬度の点では本
発明のものとほとんど同じであるけれども抗折力(TR
8>が低く、切削試験における摩耗量が多く、チップ欠
損までの切削回数の少ないものであり不満足な性能であ
った。From the above results, ■WC and MO as group a metal carbides.
Sample 1-8 of the comparative example, in which the total amount of 2C exceeds 45% and component (b) exceeds 40%, has almost the same hardness as that of the present invention, but has a lower transverse rupture strength. (T.R.
8> was low, the amount of wear in the cutting test was large, and the number of cuttings until the chip broke was small, resulting in unsatisfactory performance.
又、逆に■a族金属炭化物としてMO2Cが1%と(b
)成分が3%未満の比較例の試料1−9はTR3及び硬
度が低く、切削試験においても摩耗量が多く、チップの
欠損までの切削回数も極端に少なかった。又、<d )
成分である炭化アルミニウムを全く含まない比較例の試
料1−10も同様に不満足な性能であり、特に、チップ
欠損までの切削回数が少なかった。又、(a )成分が
5%未満である比較例の試料1−11及び(C)成分が
2.85%未満である比較例の試料1−12は硬度及び
摩耗■は問題ないがチップ欠損までの切削回数が少なか
った。又、(C)成分が30%を越える比較例の試料1
−13、<d)成分が8%を越える比較例の試料1−1
4及び(e)成分の胃換量が40%を越える比較例の試
料1−15は硬度、摩耗量、チップ欠損までの切削回数
ともに不満足であり、特に試料1−13の切削試験にお
ける結果は極端に低い性能であった。Also, conversely, if MO2C is 1% and (b
) Comparative sample 1-9 with a component of less than 3% had low TR3 and hardness, had a large amount of wear in the cutting test, and had an extremely small number of cuttings until chipping. Also, <d)
Comparative sample 1-10, which did not contain any aluminum carbide as a component, had similarly unsatisfactory performance, and in particular, the number of cuttings until chip breakage was small. In addition, Comparative Example Sample 1-11, in which the (a) component is less than 5%, and Comparative Example Sample 1-12, in which the (C) component is less than 2.85%, have no problems with hardness and wear (■), but have chip defects. The number of cuts until then was small. In addition, sample 1 of a comparative example in which the component (C) exceeds 30%
-13, <d) Comparative example sample 1-1 with component exceeding 8%
Comparative sample 1-15, in which the amount of gastric excretion of components 4 and (e) exceeds 40%, was unsatisfactory in terms of hardness, wear amount, and number of cuts until chip breakage, and in particular, the results of the cutting test for sample 1-13 were unsatisfactory. The performance was extremely low.
実施例2
同様に第1表の原料粉末を使用し、第4表に示す各実施
例の成分組成に配合し、その後、前記実施例1〜7と同
じ方法で切削工具用チップを得、同様に抗折力<TR8
)と硬度を測定し、第5表に示す切削条件で切削試験を
行った。得られた結果を各実施例の組成と共に第4表に
併記した。尚、比較例のサーメットも同方法で作成し同
様な測定を行い第4表に併記した。但し、比較例6につ
いては焼結温度1350℃以下では焼結不可能であった
ので、別に1450℃で1時開焼結処理を行った。Example 2 Similarly, the raw material powders shown in Table 1 were used and blended into the component compositions of each example shown in Table 4. Thereafter, chips for cutting tools were obtained in the same manner as in Examples 1 to 7. Transverse rupture strength<TR8
) and hardness were measured, and a cutting test was conducted under the cutting conditions shown in Table 5. The obtained results are listed in Table 4 together with the composition of each example. Incidentally, a cermet of a comparative example was also prepared by the same method and measured in the same manner, and is also listed in Table 4. However, in Comparative Example 6, it was impossible to sinter at a sintering temperature of 1350°C or lower, so a separate 1-hour open sintering process was performed at 1450°C.
以上の結果から、IV aあるいはVa族金属窒化物と
してTiN及びNbNの合計が41%と大量に配合され
た比較例の試料2−6は丁R8では優れるが、硬度が低
く、切削試験の摩耗−及び塑性変形量が大きく、不満足
な性能であった。又、逆に■a及びVa族金属窒化物を
含まない比較例の試料2−7は硬度が低く、又TR3に
おいてはかなり低く、切削試験の摩耗層及び塑性変形量
は極端に大きく、不満足な性能であった。更に、炭化ア
ルミニウムを全く含まない比較例の試料2−8は、硬度
、切削試験は上記試料2−7より更に悪い性能であった
。From the above results, Comparative Example Sample 2-6, which contains a large amount of TiN and NbN as IV a or Va group metal nitrides, with a total of 41%, is excellent in R8, but has low hardness and wear in the cutting test. - and the amount of plastic deformation was large, resulting in unsatisfactory performance. On the other hand, sample 2-7 of the comparative example, which does not contain group (a) and Va group metal nitrides, has a low hardness and is considerably low in TR3, and the wear layer and plastic deformation amount in the cutting test are extremely large, which is unsatisfactory. It was performance. Furthermore, Comparative Sample 2-8, which did not contain any aluminum carbide, had even worse performance in hardness and cutting tests than Sample 2-7.
又、本発明の試料2−1と比較例の試料2−8とは、は
とんど同一の組成であるが炭化アルミニウムを配合した
試料2−1の方は1340℃で焼結でき、前記の如<1
450℃でなければ焼結しない試料2−8よりかなり低
温で焼結し、本発明は、省エネルギーにも貢献するもの
である。In addition, sample 2-1 of the present invention and sample 2-8 of the comparative example have almost the same composition, but sample 2-1 containing aluminum carbide can be sintered at 1340°C, and the above-mentioned sample 2-1 has the same composition. like <1
It was sintered at a much lower temperature than Sample 2-8, which was not sintered at 450°C, and the present invention also contributes to energy saving.
代理人 弁理士 定立 勉Agent: Patent Attorney Tsutomu Setatetsu
Claims (1)
)成分から成ることを特徴とする強靭サーメット。 <a > 元素周期律表のIV a及びva族金属窒
化物から選ばれた1種又は2種以上:5〜30重量% (b)Via族金属及び該金属炭化物から選ばれた1種
又は2種以上:3〜40重饅% (C) 鉄族金属から選ばれた1種又は2種以上:2
.85〜30重量% (d ) 炭化アルミニウム:0.15〜8重−%(
e ) 炭化チタン及び不可避不純物:残部2 〈e
)成分中、炭化チタンの40%以下がIV a及びVa
M金属炭化物から選ばれた1種又は2種以上によって置
換されたものである特許請求の範囲第1項記載の強靭サ
ーメット。 3 (a)成分が化学式Ti N、Zr N、HfN、
VN、Nb N及びTaNから選ばれた1種又は2種以
上、(b)成分が化学式Cr 、MO、W、MO2C及
びWCから選ばれた1種又は2種以上及び(C)成分が
化学式Ni1COから選ばれた1種又は2種以上である
特許請求の範囲第1項若しくは第2項記載の強靭サーメ
ット。[Claims] 1. The following (a), (b), (C), (d) and (e)
) A strong cermet characterized by consisting of the following components. <a> One or more selected from IV a and Va group metal nitrides of the Periodic Table of the Elements: 5 to 30% by weight (b) One or two selected from Via group metals and their metal carbides Species or more: 3-40% (C) One or more selected from iron group metals: 2
.. 85-30% by weight (d) Aluminum carbide: 0.15-8% by weight (
e) Titanium carbide and inevitable impurities: remainder 2 <e
), less than 40% of titanium carbide is IV a and Va
The tough cermet according to claim 1, which is substituted with one or more selected from M metal carbides. 3 (a) Component has the chemical formula TiN, ZrN, HfN,
One or more types selected from VN, Nb N, and TaN, (b) component has the chemical formula Cr, one or more types selected from MO, W, MO2C, and WC, and (C) component has the chemical formula Ni1CO. The tough cermet according to claim 1 or 2, which is one or more selected from.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP6457082A JPS58181845A (en) | 1982-04-16 | 1982-04-16 | Tough cermet |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP6457082A JPS58181845A (en) | 1982-04-16 | 1982-04-16 | Tough cermet |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS58181845A true JPS58181845A (en) | 1983-10-24 |
JPS6334217B2 JPS6334217B2 (en) | 1988-07-08 |
Family
ID=13262010
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP6457082A Granted JPS58181845A (en) | 1982-04-16 | 1982-04-16 | Tough cermet |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS58181845A (en) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS63168239A (en) * | 1986-12-27 | 1988-07-12 | Kyocera Corp | Tool for sealing metal case for electronic part |
WO2010050493A1 (en) * | 2008-10-29 | 2010-05-06 | 京セラ株式会社 | Ceramic for decorative parts and decorative parts |
JPWO2010087092A1 (en) * | 2009-01-28 | 2012-07-26 | 京セラ株式会社 | Ceramics and decorative parts for decorative parts |
-
1982
- 1982-04-16 JP JP6457082A patent/JPS58181845A/en active Granted
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS63168239A (en) * | 1986-12-27 | 1988-07-12 | Kyocera Corp | Tool for sealing metal case for electronic part |
WO2010050493A1 (en) * | 2008-10-29 | 2010-05-06 | 京セラ株式会社 | Ceramic for decorative parts and decorative parts |
JP5404643B2 (en) * | 2008-10-29 | 2014-02-05 | 京セラ株式会社 | Ceramics and decorative parts for decorative parts |
JPWO2010087092A1 (en) * | 2009-01-28 | 2012-07-26 | 京セラ株式会社 | Ceramics and decorative parts for decorative parts |
Also Published As
Publication number | Publication date |
---|---|
JPS6334217B2 (en) | 1988-07-08 |
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