JP2686335B2 - Sintered materials for tools - Google Patents
Sintered materials for toolsInfo
- Publication number
- JP2686335B2 JP2686335B2 JP2000074A JP7490A JP2686335B2 JP 2686335 B2 JP2686335 B2 JP 2686335B2 JP 2000074 A JP2000074 A JP 2000074A JP 7490 A JP7490 A JP 7490A JP 2686335 B2 JP2686335 B2 JP 2686335B2
- Authority
- JP
- Japan
- Prior art keywords
- boron nitride
- cubic boron
- powder
- range
- sintered material
- 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
- 239000000463 material Substances 0.000 title claims description 25
- 239000000843 powder Substances 0.000 claims description 25
- 229910052582 BN Inorganic materials 0.000 claims description 22
- PZNSFCLAULLKQX-UHFFFAOYSA-N Boron nitride Chemical compound N#B PZNSFCLAULLKQX-UHFFFAOYSA-N 0.000 claims description 22
- 229910052751 metal Inorganic materials 0.000 claims description 13
- 239000002184 metal Substances 0.000 claims description 13
- TWNQGVIAIRXVLR-UHFFFAOYSA-N oxo(oxoalumanyloxy)alumane Chemical compound O=[Al]O[Al]=O TWNQGVIAIRXVLR-UHFFFAOYSA-N 0.000 claims description 10
- RVTZCBVAJQQJTK-UHFFFAOYSA-N oxygen(2-);zirconium(4+) Chemical compound [O-2].[O-2].[Zr+4] RVTZCBVAJQQJTK-UHFFFAOYSA-N 0.000 claims description 7
- 229910001928 zirconium oxide Inorganic materials 0.000 claims description 7
- 239000013078 crystal Substances 0.000 claims description 6
- 239000000203 mixture Substances 0.000 claims description 6
- 238000005245 sintering Methods 0.000 claims description 6
- HBMJWWWQQXIZIP-UHFFFAOYSA-N silicon carbide Chemical compound [Si+]#[C-] HBMJWWWQQXIZIP-UHFFFAOYSA-N 0.000 claims description 5
- 229910010271 silicon carbide Inorganic materials 0.000 claims description 4
- 238000010438 heat treatment Methods 0.000 claims description 3
- 239000011230 binding agent Substances 0.000 description 22
- 239000002245 particle Substances 0.000 description 13
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 8
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 6
- 238000012545 processing Methods 0.000 description 6
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 5
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 5
- 229910045601 alloy Inorganic materials 0.000 description 5
- 239000000956 alloy Substances 0.000 description 5
- 239000002994 raw material Substances 0.000 description 5
- 229910018072 Al 2 O 3 Inorganic materials 0.000 description 4
- 229910052782 aluminium Inorganic materials 0.000 description 4
- 239000011248 coating agent Substances 0.000 description 4
- 238000000576 coating method Methods 0.000 description 4
- 229910003460 diamond Inorganic materials 0.000 description 4
- 239000010432 diamond Substances 0.000 description 4
- 230000000694 effects Effects 0.000 description 4
- 239000011780 sodium chloride Substances 0.000 description 4
- 229910000760 Hardened steel Inorganic materials 0.000 description 3
- NRTOMJZYCJJWKI-UHFFFAOYSA-N Titanium nitride Chemical compound [Ti]#N NRTOMJZYCJJWKI-UHFFFAOYSA-N 0.000 description 3
- 239000010936 titanium Substances 0.000 description 3
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
- 229910000831 Steel Inorganic materials 0.000 description 2
- QCWXUUIWCKQGHC-UHFFFAOYSA-N Zirconium Chemical compound [Zr] QCWXUUIWCKQGHC-UHFFFAOYSA-N 0.000 description 2
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 2
- 229910052799 carbon Inorganic materials 0.000 description 2
- 239000010941 cobalt Substances 0.000 description 2
- 229910017052 cobalt Inorganic materials 0.000 description 2
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 description 2
- 230000006866 deterioration Effects 0.000 description 2
- 239000011261 inert gas Substances 0.000 description 2
- 229910000765 intermetallic Inorganic materials 0.000 description 2
- 229910052742 iron Inorganic materials 0.000 description 2
- 230000014759 maintenance of location Effects 0.000 description 2
- 150000002739 metals Chemical class 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- 229910052759 nickel Inorganic materials 0.000 description 2
- 238000011160 research Methods 0.000 description 2
- 239000010959 steel Substances 0.000 description 2
- 229910052719 titanium Inorganic materials 0.000 description 2
- UONOETXJSWQNOL-UHFFFAOYSA-N tungsten carbide Chemical compound [W+]#[C-] UONOETXJSWQNOL-UHFFFAOYSA-N 0.000 description 2
- -1 Further Inorganic materials 0.000 description 1
- QYEXBYZXHDUPRC-UHFFFAOYSA-N B#[Ti]#B Chemical compound B#[Ti]#B QYEXBYZXHDUPRC-UHFFFAOYSA-N 0.000 description 1
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 1
- 238000005299 abrasion Methods 0.000 description 1
- 239000000853 adhesive Substances 0.000 description 1
- 230000001070 adhesive effect Effects 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
- 239000000919 ceramic Substances 0.000 description 1
- 239000010730 cutting oil Substances 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 239000000835 fiber Substances 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 150000001247 metal acetylides Chemical class 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 150000004767 nitrides Chemical class 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 230000001737 promoting effect Effects 0.000 description 1
- 239000003870 refractory metal Substances 0.000 description 1
- 230000002787 reinforcement Effects 0.000 description 1
- VSZWPYCFIRKVQL-UHFFFAOYSA-N selanylidenegallium;selenium Chemical compound [Se].[Se]=[Ga].[Se]=[Ga] VSZWPYCFIRKVQL-UHFFFAOYSA-N 0.000 description 1
- 229910052710 silicon Inorganic materials 0.000 description 1
- 239000010703 silicon Substances 0.000 description 1
- 229910000679 solder Inorganic materials 0.000 description 1
- 230000007704 transition Effects 0.000 description 1
- 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 description 1
- WFKWXMTUELFFGS-UHFFFAOYSA-N tungsten Chemical compound [W] WFKWXMTUELFFGS-UHFFFAOYSA-N 0.000 description 1
- 229910052721 tungsten Inorganic materials 0.000 description 1
- 239000010937 tungsten Substances 0.000 description 1
- 238000001771 vacuum deposition Methods 0.000 description 1
- 229910052726 zirconium Inorganic materials 0.000 description 1
Landscapes
- Cutting Tools, Boring Holders, And Turrets (AREA)
- Ceramic Products (AREA)
Description
【発明の詳細な説明】 〈産業上の利用分野〉 本発明は、焼入鋼や超硬合金等の高硬度材料或いは耐
熱合金等の切削加工や塑性加工の際に用いられる工具用
焼結材料に関する。DETAILED DESCRIPTION OF THE INVENTION <Industrial field of application> The present invention relates to a sintered material for a tool used in cutting or plastic working a high hardness material such as hardened steel or cemented carbide or a heat resistant alloy. Regarding
〈従来の技術〉 焼入鋼或いはニッケル基耐熱合金やコバルト基耐熱合
金等の高硬度材料を加工する場合、一般にはタングステ
ン(W)等の高融点金属の炭化物粉末を鉄(Fe)やコバ
ルト(Co)やニッケル(Ni)等の鉄系金属で焼結結合さ
せた超硬合金が利用されてきている。<Prior Art> When processing hardened steel or high hardness materials such as nickel-base heat-resistant alloys and cobalt-base heat-resistant alloys, generally, carbide powder of refractory metal such as tungsten (W) is used for iron (Fe) or cobalt ( Cemented carbides that have been sintered and bonded with iron-based metals such as Co) and nickel (Ni) have been used.
近年、上述した超硬合金が工具としてではなく、加工
対象物として採用されつつあることに加え、加工条件に
対する厳しい要求に対応するため、より高性能な工具と
して焼結ダイヤモンドや立方晶窒化硼素(CBN)焼結体
等を用いたものが開発されている。焼結ダイヤモンドは
ダイヤモンドの粉粒を超硬合金を結合剤として高温高圧
下で焼結したものであるが、炭素(C)との親和力が強
い鋼等の加工には根本的に不向きである。この点、ダイ
ヤモンドに次ぐ硬度のCBN焼結体は鉄系金属との反応が
少ないことから、ダイヤモンド以外のあらゆる加工対象
物、特に焼入鋼や超硬合金等の高硬度材料の他にニッケ
ル基耐熱合金やコバルト基耐熱合金等の加工に有効であ
る。In recent years, the above-mentioned cemented carbide is being adopted not as a tool but as an object to be processed, and in order to meet strict requirements for processing conditions, sintered diamond and cubic boron nitride ( CBN) sintered products have been developed. Sintered diamond is obtained by sintering diamond powder particles at a high temperature and high pressure using a cemented carbide as a binder, but is fundamentally unsuitable for processing steel having a strong affinity for carbon (C). In this regard, the CBN sintered body, which has the second highest hardness after diamond, has little reaction with iron-based metals, and therefore, in addition to high-hardness materials such as hardened steel and cemented carbide, nickel-based It is effective for processing heat-resistant alloys and cobalt-based heat-resistant alloys.
従来のCBN焼結体は、CBNの粉粒に結合剤として炭化チ
タンや窒化チタン等のセラミックスを混ぜ、これらを高
温高圧下で焼結したものがほとんどである。結合剤とし
ては、上記の他に硅素やジルコニウム(Zr)の窒化物、
更にはアルミニウム(Al)とチタン(Ti)との金属間化
合物やAlとZrとの金属間化合物等が知られている。Most conventional CBN sintered bodies are obtained by mixing ceramics such as titanium carbide and titanium nitride as a binder with CBN powder and sintering them under high temperature and high pressure. As the binder, in addition to the above, nitrides of silicon and zirconium (Zr),
Further, intermetallic compounds of aluminum (Al) and titanium (Ti), intermetallic compounds of Al and Zr, etc. are known.
〈発明が解決しようとする課題〉 従来のCBN焼結体を用いた工具では、高温領域下で結
合相の硬度低下が発生するため、工具自体が高温となる
ような加工の際には、結合相からのCBNの粉粒の脱落が
起こり易く、耐摩耗性の低下を招来するものが多い。ま
た、このような工具を長時間の自動運転を行う加工機械
に組込む場合、突発的な工具欠損が発生することは、加
工機械等の損傷や設備稼動率の低下等の点で絶対に避け
るべきであるが、従来のこの種のCBN焼結体は高い硬度
を追求するあまり、靱性が充分なものとは云えなかっ
た。<Problems to be Solved by the Invention> In a tool using a conventional CBN sintered body, the hardness of the binder phase decreases in a high temperature region, so when the tool itself is processed at high temperature, CBN powder particles easily fall off from the phase, often leading to reduced wear resistance. In addition, when such a tool is installed in a processing machine that performs automatic operation for a long time, it is absolutely necessary to avoid sudden tool loss from damage to the processing machine, etc. However, the conventional CBN sintered body of this type pursues a high hardness, and cannot be said to have sufficient toughness.
本発明者らは、酸化アルミニウム(アルミナ:Al
2O3)が窒化チタンや硼化チタン等と同程度の常温硬度
を有し、しかも600から800℃の範囲の高温状態における
硬度がこれらよりも高い点に着目して、実験を進め、こ
のAl2O3がCBNの結合材として有効であることも見い出
した。The present inventors have found that aluminum oxide (alumina: Al
2 O 3 ) has the same room temperature hardness as titanium nitride, titanium boride, etc., and the hardness in the high temperature range of 600 to 800 ° C. is higher than these. It has also been found that Al 2 O 3 is effective as a binder for CBN.
この際、CBN粒と結合材の粒界のぬれ性を改善し、接
着性を向上することを目的としてAl及びTiのうち少なく
とも一方の粉粒を添加したが、結合材単味焼結体での金
属添加量の影響を調べた結果から上記粒界の特性向上の
ために添加した金属粉粒が、結合材相に対しては焼結性
を低めていることがわかった。この対策として、CBN粒
の表面に金属をコーティングすることによりCBN粒と結
合材相の粒界のみに金属を存在させるとの着想を得、実
験でその効果を確認した。At this time, in order to improve the wettability of the grain boundary between the CBN grains and the binder, and at least one of Al and Ti powder grains was added for the purpose of improving the adhesiveness. As a result of investigating the effect of the amount of added metal, it was found that the metal powder particles added to improve the properties of the grain boundary have low sinterability with respect to the binder phase. As a countermeasure against this, the idea of coating the surface of CBN grains with metal so that the metal is present only at the grain boundaries between the CBN grains and the binder phase was confirmed by experiments.
〈課題を解決するための手段〉 本発明はかかる実験結果を踏まえてなされたもので、
40〜90体積%の立方晶窒化硼素の粉粒と、5〜55体積%
の酸化ジルコニウムの粉粒及び酸化アルミニウムの粉粒
との混合物に炭化ケイ素の針状結晶を添加したものを超
高圧発生装置により40〜60キロバールの範囲で加圧しつ
つ1200℃〜1800℃の範囲で加熱し焼結してなる工具用焼
結材料において、立方晶窒化硼素の粉末に金属の被膜を
施したことを特徴とする。また、立方晶窒化硼素の粒径
が1乃至3マイクロメートルの範囲にあり、且つ金属の
被膜厚さが10乃至1000オングストロームの範囲にあるこ
とを特徴とする。<Means for Solving the Problems> The present invention has been made based on such experimental results,
40-90% by volume of cubic boron nitride powder particles, and 5-55% by volume
A mixture of zirconium oxide powder particles and aluminum oxide powder particles to which needle-like crystals of silicon carbide were added was pressurized in the range of 40 to 60 kbar with an ultra-high pressure generator, while the temperature was in the range of 1200 to 1800 ° C. A sintered material for a tool obtained by heating and sintering is characterized in that a powder of cubic boron nitride is coated with a metal film. The cubic boron nitride is characterized in that its grain size is in the range of 1 to 3 micrometers, and the film thickness of the metal is in the range of 10 to 1000 angstroms.
この場合、金属の破膜が施された立方晶窒化硼素の粉
粒と、酸化ジルコニウムの粉粒及び酸化アルミニウムの
粉粒の混合物に炭化ケイ素の針状結晶を添加したもの
を、均一に混合撹拌した後、これを高融点材料の容器に
装入してベルト型超高圧発生装置等の超高圧発生装置に
より40〜60キロバール(Kb)の範囲で加圧しつつ1200〜
1800℃の範囲で加熱し、この状態を0.5〜30分程度保持
することにより工具用焼結材料を得る。In this case, a mixture of cubic boron nitride powder particles coated with a metal film, zirconium oxide powder particles and aluminum oxide powder particles to which needle-like crystals of silicon carbide were added was uniformly mixed and stirred. Then, this is charged into a container of high melting point material, and while being pressurized in the range of 40 to 60 kilobar (Kb) by an ultrahigh pressure generator such as a belt type ultrahigh pressure generator, 1200 to
The sintered material for tools is obtained by heating in the range of 1800 ° C and maintaining this state for about 0.5 to 30 minutes.
〈作用〉 立方晶窒化硼素は工具用焼結材料としての主体をなす
ものであり、これが40体積%未満では立方晶窒化硼素自
体の硬度を反映させることが困難となり、充分な耐摩耗
性を得られない。逆に、この立方晶窒化硼素が90体積%
を超えると、焼結時にその一部が六方晶に相転位を起こ
して焼結性が悪化するため、靱性の低下により微小なチ
ッピングや欠損が発生する。<Action> Cubic boron nitride is the main material as a sintered material for tools, and if it is less than 40% by volume, it becomes difficult to reflect the hardness of cubic boron nitride itself, and sufficient abrasion resistance is obtained. I can't. On the contrary, this cubic boron nitride contains 90% by volume.
If it exceeds 1.0, part of the hexagonal crystals undergo phase transition during sintering to deteriorate the sinterability, so that minute chipping or chipping occurs due to deterioration in toughness.
一方、酸化ジルコニウムと酸化アルミニウムとの混合
物は立方晶窒化硼素の結合剤としての特性を発揮するた
め、これらが5体積%或いは4体積%未満では工具用焼
結材料中に占める立方晶窒化硼素の量が相対的に多くな
り過ぎ、焼結性が悪化して耐摩耗性や靱性の低下を招来
する。逆に、この混合物が55体積%或いは50体積%を超
えると、立方晶窒化硼素の量が相対的に少なくなり過ぎ
てしまい、立方晶窒化硼素自体の硬度を工具用焼結材料
に反映させることが困難となり、やはり耐摩耗性の低下
を招くこととなる。なお、一般的な傾向として酸化アル
ミニウムに対する酸化ジルコニウムの割合を多くするほ
ど靱性が向上し、逆に酸化アルミニウムの割合を多くす
るほど結合相の硬度が高くなる。以上の兼ね合いから、
酸化アルミニウムに対して酸化ジルコニウムを1から30
体積%の割合に収めることが望ましく、特に1から10体
積%の範囲が好適である。On the other hand, since a mixture of zirconium oxide and aluminum oxide exhibits the property as a binder of cubic boron nitride, if the content of these is less than 5% by volume or less than 4% by volume, the cubic boron nitride content in the sintered material for tools will be reduced. If the amount is too large, the sinterability deteriorates, leading to deterioration in wear resistance and toughness. On the other hand, if this mixture exceeds 55% by volume or 50% by volume, the amount of cubic boron nitride will be too small, and the hardness of cubic boron nitride itself should be reflected in the sintered material for tools. Becomes difficult, and the wear resistance is also deteriorated. As a general tendency, the toughness is improved as the ratio of zirconium oxide to aluminum oxide is increased, and conversely, the hardness of the binder phase is increased as the ratio of aluminum oxide is increased. From the above tradeoffs,
1 to 30 zirconium oxide to aluminum oxide
It is desirable that the content be within a volume% ratio, and a range of 1 to 10 volume% is particularly preferable.
また、立方晶窒化硼素粒表面にコーティングするAlの
厚みについては、10オングストローム以下では金属添加
による立方晶窒化硼素粒と結合相のぬれ性改善、接着力
向上等の効果が現れず、逆に100オングストロームより
厚くなると焼結後に立方晶窒化硼素粒と結合相の粒界に
残留し、粒界の強度を低下させるように働くため耐摩耗
性が悪化してしまう。Regarding the thickness of Al coated on the surface of the cubic boron nitride particles, if the thickness is 10 angstroms or less, the effect of improving the wettability of the cubic boron nitride particles and the binder phase by the addition of metal, improving the adhesive strength, etc. does not appear, and conversely 100 If the thickness is thicker than angstrom, the cubic boron nitride grains and the binder phase remain at the grain boundaries after sintering, and the strength of the grain boundaries is reduced, so that the wear resistance deteriorates.
〈実施例〉 無触媒法で合成された1から3マイクロメートル(μ
m)の範囲の粒径の立方晶窒化硼素(CBN)で、その表
面に真空蒸着法によりアルミニウム(Al)を10オングス
トローム(Å),100Å,1000Åの厚みでコーティングし
たCBN粒と、平均粒径がそれぞれ0.3μmの酸化ジルコニ
ウム(ZrO2)と酸化アルミニウム(Al2O3)とからなり
且つこれらの体積比を4:96(=ZrO2:Al2O3)に調整し
た混合物と、更に結合相の靱性を向上させるための炭化
ケイ素(SiC)の針状結晶とを炭化タングステン(WC)
基超硬合金で内張りした小形の遊星運動型ミル内に装入
し、更にこれらの混合を促進する目的でこれら粉粒の総
体積の35%に相当する量のメチルアルコールをミル内に
加え、蓋をしてこれらを3時間混練した。そして、不活
性ガス雰囲気にてミルの蓋を取り、ミルを120℃に加熱
してメチルアルコールを蒸発させ、混練された原料粉体
の乾燥を行った。<Example> 1 to 3 micrometers (μ
m) cubic boron nitride (CBN) with a grain size in the range of 10 angstrom (Å), 100 Å, 1000 Å with aluminum (Al) coated on its surface by vacuum deposition, and the average grain size. Is composed of zirconium oxide (ZrO 2 ) and aluminum oxide (Al 2 O 3 ) each having a volume ratio of 0.3 μm, and the volume ratio of these is adjusted to 4:96 (= ZrO 2 : Al 2 O 3 ). Silicon carbide (SiC) needle crystals to improve the toughness of the phase and tungsten carbide (WC)
It is charged into a small planetary motion type mill lined with a base cemented carbide, and the amount of methyl alcohol corresponding to 35% of the total volume of these powder particles is added to the mill for the purpose of promoting the mixing of these, With the lid on, these were kneaded for 3 hours. Then, the lid of the mill was removed in an inert gas atmosphere, and the mill was heated to 120 ° C. to evaporate the methyl alcohol, and the kneaded raw material powder was dried.
一方、塩化ナトリウム(NaCl)の粉粒を内径8ミリメ
ートル、長さ10ミリメートルの円筒状に加圧成形してい
るNaCl製の容器本体に、同様にして作成したNaCl製の下
蓋を一体的に取付け、これらの内面に厚さ20μmのジル
コニウム箔を張り付け、更にこの中に直径7.8ミリメー
トル、厚さ2ミリメートルのWC基超硬合金製の円板を載
置したものを用意しておく。On the other hand, a sodium chloride (NaCl) powder particle is pressure-molded into a cylindrical shape with an inner diameter of 8 mm and a length of 10 mm, and a NaCl lower lid made in the same manner is integrally formed on the container body. A zirconium foil having a thickness of 20 μm is attached to these inner surfaces, and a disk made of WC-based cemented carbide having a diameter of 7.8 mm and a thickness of 2 mm is placed therein.
そして、乾燥終了後の前記原料粉体を不活性ガス雰囲
気にてこの容器本体内の前記円板上に6ミリメートルの
厚みになるように装入して突棒で突き固め、更にこの上
に前述したのと同一なWC基超硬合金製の円板を載置し、
またこの上に厚さ20μmのジルコニウム箔を重ねたの
ち、前述と同様にして作成したNaCl製の上蓋を容器本体
に嵌め込み、これら容器本体と下蓋と上蓋とからなる容
器内に原料粉末を密封する。Then, the raw material powder after completion of the drying is charged in the inert gas atmosphere onto the disk in the container body so as to have a thickness of 6 mm, and is compacted with a protruding rod. Place the same WC-based cemented carbide disk as
Also, after stacking a 20 μm thick zirconium foil on this, insert the NaCl upper lid created in the same way as above into the container body, and seal the raw material powder in the container consisting of these container body, lower lid and upper lid. To do.
次に、超高圧発生装置に上述した容器を取付け、50Kb
の圧力と1650℃の温度とを30分間保持し、原料粉末を焼
結させて両端にWC基超硬合金が結合した円柱状の工具用
焼結材料を得た。そして、この工具用焼結材料を前記円
板が結合した状態のまま切り出してバイト用の切刃を仕
上げ、これを予め用意しておいた四角形のWC基超硬合金
製チップに銀ろうを介して固定しすくい角0度、逃げ角
5度、ノーズ曲率半径が1ミリメートルのバイトを作成
した。Next, the above-mentioned container was attached to the ultra-high pressure generator, and 50 Kb
The pressure was maintained at a temperature of 1650 ° C. for 30 minutes, and the raw material powder was sintered to obtain a cylindrical sintered material for a tool having a WC-based cemented carbide bonded to both ends. Then, this sintered material for tools is cut out in a state where the discs are bonded to finish the cutting edge for the bite, and this is prepared in advance with a rectangular WC-based cemented carbide tip through silver solder. A bite having a rake angle of 0 °, a clearance angle of 5 ° and a nose radius of curvature of 1 mm was prepared.
このバイトを用い、ロックウエル硬さ(Cスケール)
が62の丸棒状をなす高炭素軸受鋼(SUJ2)に対して切削
速度が毎分170メートル、切込み量が20μm、バイトの
送り速度が主軸一回転当り20μmとなるようにして100
メートルの長さに相当する距離で旋削した後、切刃の逃
げ面の摩耗量及びこの切刃を構成するCBN焼結材料のビ
ッカース硬さを、前記原料粉末を構成する各粉粒の比率
を変えて測定した。なおこの旋削加工中には切削油を噴
霧供給した。Rockwell hardness (C scale)
Is 62 round bar shaped high carbon bearing steel (SUJ2) with a cutting speed of 170 meters per minute, a depth of cut of 20 μm and a bite feed rate of 20 μm per revolution of the spindle.
After turning at a distance equivalent to the length of the meter, the wear amount of the flank of the cutting edge and the Vickers hardness of the CBN sintered material that constitutes this cutting edge, the ratio of each powder grain that constitutes the raw material powder. It changed and measured. The cutting oil was spray-supplied during the turning process.
これらの測定結果を第1表及び第2表に示すが、ちな
みに窒化チタンを結合剤として使用した市販のCBN焼結
材料を用いた場合のビッカース硬さは2500、切刃の逃げ
面摩耗幅は40μmであった。These measurement results are shown in Table 1 and Table 2. By the way, when using a commercially available CBN sintered material using titanium nitride as a binder, the Vickers hardness is 2500, and the flank wear width of the cutting edge is It was 40 μm.
尚、本実施例において、CBN粒にAlをコーティングし
たことにより、CBN粒と結合相の粒界の密着性が改善さ
れ、従来発明者らが製作したAl添加のCBN焼結材料に比
べ、耐摩耗性の改善が認められた。すなわちAl添加のCB
N焼結材料で第2表記載のNo.13と同一の組成のCBN焼結
材料は、逃げ面摩耗幅が34μmであったのに対し、本実
施例では逃げ面摩耗幅が28μmであり、CBN 粒へのAlコーティングの効果が表われている。Incidentally, in this example, by coating the CBN grains with Al, the adhesion between the CBN grains and the grain boundary of the binder phase was improved, and compared with the Al-added CBN sintered material produced by the conventional inventors, Improvement in wear resistance was observed. That is, CB with Al added
The CBN sintered material having the same composition as No. 13 in Table 2 as the N sintered material had a flank wear width of 34 μm, whereas the flank wear width was 28 μm in the present example. CBN The effect of Al coating on the grains is shown.
上述した工具用焼結材料は、高温時での硬度が高いAl
3O3を主体とする結合剤を用いたので、特に高温時での
耐摩耗性を改善することができさらに、CBN粒の表面にA
lコーティングを施こしたことにより、CBN粒と結合相の
密着性が向上しCBN粒の結合相による保持能力が従来の
ものよりも向上する。また、結合相にSiCの針状結晶を
添加したものでは、繊維強化による結合相の高靱化が可
能となり、耐摩耗性の向上と同時にチッピングや欠損の
少ない工具用焼結材料を提供できる。The above-mentioned sintered materials for tools have high hardness at high temperatures
Since a binder consisting mainly of 3 O 3 is used, wear resistance can be improved especially at high temperatures.
By applying the coating, the adhesion between CBN grains and the binder phase is improved, and the retention capacity of the CBN grains by the binder phase is improved compared to the conventional one. Further, in the case where SiC needle crystals are added to the binder phase, it is possible to increase the toughness of the binder phase by fiber reinforcement, and it is possible to provide a sintered material for tools with improved wear resistance and less chipping and chipping.
〈発明の効果〉 本発明の工具用焼結材料は、高温時での硬度が高い酸
化アルミニウムを主体とする結合剤を用いたので、高温
時での耐摩耗性を改善することができる。また、立方晶
窒化硼素の表面に金属の被膜を施したので、立方晶窒化
硼素粒と結合相の密着性が向上し、立方晶窒化硼素粒の
結合相による保持能力が向上した。<Effects of the Invention> Since the sintered material for a tool of the present invention uses a binder mainly composed of aluminum oxide, which has a high hardness at high temperatures, it is possible to improve wear resistance at high temperatures. Further, since the surface of the cubic boron nitride was coated with a metal, the adhesion between the cubic boron nitride grains and the binder phase was improved, and the retention capacity of the cubic boron nitride grains by the binder phase was improved.
───────────────────────────────────────────────────── フロントページの続き (72)発明者 深谷 保博 広島県広島市西区観音新町4丁目6番22 号 三菱重工業株式会社広島研究所内 (72)発明者 角田 英雄 長崎県長崎市飽の浦町1番1号 三菱重 工業株式会社長崎研究所内 (72)発明者 安田 福司 東京都千代田区丸の内2丁目5番1号 三菱重工業株式会社内 (56)参考文献 特開 平2−302371(JP,A) 特開 昭61−168569(JP,A) ─────────────────────────────────────────────────── ─── Continuation of the front page (72) Inventor Yasuhiro Fukaya 4-6-22 Kannon Shinmachi, Nishi-ku, Hiroshima City, Hiroshima Prefecture Mitsubishi Heavy Industries Ltd. Hiroshima Research Laboratory (72) Inventor Hideo Tsunoda 1-1, Atsunoura-cho, Nagasaki-shi, Nagasaki Prefecture No. Mitsubishi Heavy Industries Ltd. Nagasaki Research Institute (72) Inventor Fukushi Yasuda Marunouchi 2-5-1-5, Chiyoda-ku, Tokyo Mitsubishi Heavy Industries Ltd. (56) Reference JP-A-2-302371 (JP, A) Sho 61-168569 (JP, A)
Claims (2)
5〜55体積%の酸化ジルコニウムの粉末及び酸化アルミ
ニウムの粉末との混合物に炭化ケイ素の針状結晶を添加
したものを超高圧発生装置により40〜60キロバールの範
囲で加圧しつつ1200℃〜1800℃の範囲で加熱し焼結して
なる工具用焼結材料において、立方晶窒化硼素の粉末に
金属の被膜を施したことを特徴とする工具用焼結材料。1. A powder of 40 to 90% by volume of cubic boron nitride,
A mixture of 5 to 55% by volume of zirconium oxide powder and aluminum oxide powder, to which needle-like crystals of silicon carbide are added, is pressurized in the range of 40 to 60 kbar by an ultra-high pressure generator, while the temperature is 1200 to 1800 ° C. A sintered material for a tool, which is obtained by heating and sintering in the range of 1., wherein a powder of cubic boron nitride is coated with a metal film.
いて、立方晶窒化硼素の粒径が1乃至3マイクロメート
ルの範囲にあり、且つ金属の被膜厚さが10乃至1000オン
グストロームの範囲にあることを特徴とする工具用焼結
材料。2. The sintered material for a tool according to claim 1, wherein the cubic boron nitride has a grain size in the range of 1 to 3 μm, and the metal film thickness is 10 to 1000 angstroms. Sintered material for tools characterized by being in the range.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2000074A JP2686335B2 (en) | 1990-01-05 | 1990-01-05 | Sintered materials for tools |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2000074A JP2686335B2 (en) | 1990-01-05 | 1990-01-05 | Sintered materials for tools |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPH03205364A JPH03205364A (en) | 1991-09-06 |
| JP2686335B2 true JP2686335B2 (en) | 1997-12-08 |
Family
ID=11464026
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2000074A Expired - Lifetime JP2686335B2 (en) | 1990-01-05 | 1990-01-05 | Sintered materials for tools |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JP2686335B2 (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| KR101848941B1 (en) * | 2010-10-27 | 2018-04-13 | 스미또모 덴꼬오 하드메탈 가부시끼가이샤 | Sintered cubic boron nitride compact and sintered cubic boron nitride compact tool |
Families Citing this family (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP3742153B2 (en) | 1996-08-29 | 2006-02-01 | 日鉄鉱業株式会社 | Coated powder consolidated product and method for producing the same |
| KR100459518B1 (en) * | 1996-12-03 | 2005-05-18 | 스미토모덴키고교가부시키가이샤 | High Pressure Phase Boron Nitride Sintered Body |
| US8993132B2 (en) | 2010-09-01 | 2015-03-31 | Sumitomo Electric Hardmetal Corp. | Cubic boron nitride sintered body tool |
| WO2012177467A1 (en) * | 2011-06-21 | 2012-12-27 | Diamond Innovations, Inc. | Composite compacts formed of ceramics and low-volume cubic boron nitride and method of manufacture |
| JP6095162B2 (en) * | 2013-03-29 | 2017-03-15 | 住友電工ハードメタル株式会社 | Cubic boron nitride sintered body |
| JP6198142B2 (en) * | 2014-03-26 | 2017-09-20 | 三菱マテリアル株式会社 | Cutting tool made of cubic boron nitride super high pressure sintered material |
Family Cites Families (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2826585B2 (en) * | 1989-05-17 | 1998-11-18 | 工業技術院長 | Method for producing inorganic composite sintered body containing cubic boron nitride |
-
1990
- 1990-01-05 JP JP2000074A patent/JP2686335B2/en not_active Expired - Lifetime
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| KR101848941B1 (en) * | 2010-10-27 | 2018-04-13 | 스미또모 덴꼬오 하드메탈 가부시끼가이샤 | Sintered cubic boron nitride compact and sintered cubic boron nitride compact tool |
Also Published As
| Publication number | Publication date |
|---|---|
| JPH03205364A (en) | 1991-09-06 |
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