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JPS6227032B2 - - Google Patents
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JPS6227032B2 - - Google Patents

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Publication number
JPS6227032B2
JPS6227032B2 JP58020460A JP2046083A JPS6227032B2 JP S6227032 B2 JPS6227032 B2 JP S6227032B2 JP 58020460 A JP58020460 A JP 58020460A JP 2046083 A JP2046083 A JP 2046083A JP S6227032 B2 JPS6227032 B2 JP S6227032B2
Authority
JP
Japan
Prior art keywords
powder
dispersed phase
sialon
cutting
whiskers
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
Application number
JP58020460A
Other languages
Japanese (ja)
Other versions
JPS59146982A (en
Inventor
Taijiro Sugisawa
Teruyoshi Tanase
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Mitsubishi Metal Corp
Original Assignee
Mitsubishi Metal Corp
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Mitsubishi Metal Corp filed Critical Mitsubishi Metal Corp
Priority to JP58020460A priority Critical patent/JPS59146982A/en
Publication of JPS59146982A publication Critical patent/JPS59146982A/en
Publication of JPS6227032B2 publication Critical patent/JPS6227032B2/ja
Granted legal-status Critical Current

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Description

【発明の詳細な説明】[Detailed description of the invention]

この発明は、高硬度および高靭性を有し、さら
に耐摩耗性および耐熱衝撃性にすぐれ、したがつ
てこれらの特性が要求される鋼や鋳鉄などの高速
切削、並びに高送り切削および深切込み切削など
の重切削に用いられる切削工具として、さらに軸
受や線引ダイスなどの耐摩耗工具として使用した
場合にすぐれた性能を発揮するサイアロン基焼結
材料に関するものである。 従来、母相が組成式:Si6−zAlzOzN8−z(た
だし0.1≦z≦5.0)を有するβ−サイアロンで構
成され、かつ分散相がTi,Zr,Hf,Ta,Mo,お
よびWの炭化物および窒化物、並びにこれらの2
種以上の固溶体(以下これらをを総称して金属の
炭・窒化物分散相という)のうちの1種または2
種以上で構成されたサイアロン基焼結材料が切削
工具として用いられていることはよく知られると
ころである。なお、上記のβ−サイアロンは、
Si3N4粉末、Al2O3粉末、およびAlN粉末の主要粉
末からなる混合粉末をN2雰囲気中で焼結するこ
とによつて容易に形成することができるものであ
る。 しかし、上記の従来サイアロン基焼結材料は、
高硬度およびすぐれた耐摩耗性をもつ反面、靭性
が不足し、耐熱衝撃性に劣るものであるため、こ
れを特に靭性や耐熱衝撃性が要求される鋼や鋳鉄
の重切削に用いた場合には刃先に欠損が発生し易
く、短かい使用寿命しか示さないのが現状であ
る。 そこで、本発明者等は、上記の高硬度およびす
ぐれた耐摩耗性を有する従来サイアロン基焼結材
料に、高靭性およびすぐれた耐熱衝撃性を付与す
べく研究を行つた結果、上記従来サイアロン基焼
結材料における金属の炭・窒化物分散相の一部、
または全部を針状結晶(ひげ結晶)、すなわちホ
イスカーで構成すると共に、β−サイアロンを組
成式:Si6−zAlzOzN8−zで現わした場合、前記
z値を0.2〜3.0の範囲内に限定すると、この結果
のサイアロン基焼結材料は、高硬度およびすぐれ
た耐摩耗性を保持した状態で、高靭性およびすぐ
れた耐熱衝撃性をもつようになるという知見を得
たのである。 したがつて、この発明は上記知見にもとづいて
なされたものであつて、 金属の炭・窒化物分散相:2〜30容量%、 を含有し、さらに必要に応じて、 同じく分散相形成成分としてのMg,Y,Al,
Si,Ti,Zr,およびHfの酸化物(以下これらを
総称して金属の酸化物分散相という)のうちの1
種または2種以上:1〜20容量%、 を含有し、残りが母相形成成分としての組成式:
Si6−zAlzOzN8−z(ただし0.2≦z≦3.0)を有
するβ−サイアロンと不可避不純物からなる組成
を有し、かつ上記金属の炭・窒化物分散相の30容
量%以上が針状結晶(ホイスカー)で構成された
サイアロン基焼結材料に特徴を有するものであ
る。 なお、この発明のサイアロン基焼結材料におけ
る金属の炭・窒化物分散相の針状結晶は、短かい
繊維状形状を有し、通常は相互が多数個所で接触
した状態で分布しているが、この針状結晶の方向
を調製することによつて、サイアロン基焼結材料
自体の強度に方向性を付与することができるもの
である。 つぎに、この発明のサイアロン基焼結材料にお
いて成分組成を上記の通りに限定した理由を説明
する。 (a) 金属の炭・窒化物分散相 これらの成分には、材料の硬さを向上させ、も
つて耐摩耗性を向上せしめる作用があるが、その
含有量が2容量%未満では所望の耐摩耗性改善効
果が得られず、一方30容量%を越えて含有させる
と、材料の靭性が劣化するようになることから、
その含有量を2〜30容量%と定めた。 (b) 金属の酸化物分散相 これらの成分には、母相中に均一に分散して焼
結性を向上せしめると共に、結晶粒の成長を抑制
し、もつて材料の靭性および耐熱衝撃性を一段と
向上せしめる作用があるので、必要に応じて含有
されるが、その含有量が1容量%未満では前記作
用に所望の向上効果が得られず、一方20容量%を
越えて含有させても前記作用に向上効果が得られ
ず、むしろ劣化傾向が現われるようになることか
ら、その含有量を1〜20容量%を定めた。 (c) 針状結晶 その含有量が、金属の炭・窒化物分散相に対す
る割合で30容量%未満では所望の高靭性およびす
ぐれた耐熱衝撃性を確保することができないの
で、その含有量が30容量%以上となるようにしな
ければならない。また、材料中における金属の
炭・窒化物分散相の含有量が相対的に少ない場合
には針状結晶の占める割合を多くし、逆に金属の
炭・窒化物分散相の含有量が相対的に多い場合に
は相対的にその割合を少なくするとよく、これに
よつて良好な焼結性が保持され、高靭性が確保さ
れるようになるのである。 (d) zの値 zの値が0.2未満の組成を有するβ−サイアロ
ンにおいては、焼結性が悪く、かつ所望の高い硬
さ(耐摩耗性)を確保することができず、一方z
の値が3を越えた組成を有するβ−サイアロンで
は材料の靭性低下が著しくなることから、組成
式:Si6−zAlzOzN8−zにおけるzの値を0.2〜
3と定めた。 つぎに、この発明のサイアロン基焼結材料を実
施例により具体的に説明する。 実施例 原料粉末として、β−サイアロン形成用として
の平均粒径:1μmを有するSi3N4粉末、同0.6μ
mのAl2O3粉末、および同1μmのAlN粉末、さ
らに0.8〜1.5μmの範囲内の平均粒径を有する
TiC粉末、ZrC粉末、HfC粉末、NbC粉末、TaC
粉末、Mo2C粉末、およびWC粉末、同じく0.8〜
1.5μmの範囲内の平均粒径を有するTiN粉末、
ZrN粉末、HfN粉末、NbN粉末、TaN粉末、
(Ti,Hf)C粉末、(Zr,Nb,W)C粉末、
(Hf,Nb)N粉末、および(Ti,W)CN粉末、
さらにいずれも針状結晶である直径:1〜4μ
m、長さ:5〜100μmの範囲内の寸法をもつた
TiCホイスカー、ZrCホイスカー、HfCホイスカ
ー、NbCホイスカー、TaCホイスカー、TiNホイ
スカー、ZrNホイスカー、HfNホイスカー、NbN
ホイスカー、TaNホイスカー、さらに0.5〜1.5μ
mの範囲内の平均粒径を有するMgO粉末、Y2O3
粉末、Al2O3粉末、SiO2粉末、TiO2粉末、ZrO2
末、およびHfO2粉末をそれぞれ用意し、これら
原料粉末をそれぞれ第1表に示される配合組成に
配合し、ボールミル中で2時間混合した後、
1ton/cm2の圧
This invention has high hardness and toughness, and has excellent wear resistance and thermal shock resistance, and is therefore suitable for high-speed cutting of materials such as steel and cast iron, which require these characteristics, as well as high-feed cutting and deep-cutting. The present invention relates to a sialon-based sintered material that exhibits excellent performance when used as a cutting tool for heavy cutting such as bearings, wire drawing dies, and other wear-resistant tools. Conventionally, the parent phase is composed of β-sialon having the composition formula: Si 6 −zAlzOzN 8 −z (0.1≦z≦5.0), and the dispersed phase is carbides of Ti, Zr, Hf, Ta, Mo, and W. and nitrides, and these two
One or two types of solid solutions (hereinafter collectively referred to as metal carbon/nitride dispersed phase)
It is well known that sialon-based sintered materials composed of more than one species are used as cutting tools. In addition, the above β-sialon is
It can be easily formed by sintering a mixed powder consisting of the main powders of Si 3 N 4 powder, Al 2 O 3 powder, and AlN powder in an N 2 atmosphere. However, the above conventional sialon-based sintered materials
Although it has high hardness and excellent wear resistance, it lacks toughness and has poor thermal shock resistance, so it cannot be used for heavy cutting of steel or cast iron, which particularly requires toughness and thermal shock resistance. Currently, the cutting edge is prone to breakage and has a short service life. Therefore, the present inventors conducted research to impart high toughness and excellent thermal shock resistance to the conventional sialon-based sintered material, which has the above-mentioned high hardness and excellent wear resistance. Part of the metal carbon/nitride dispersed phase in the sintered material,
Alternatively, if the entire structure is composed of needle-like crystals (beard crystals), that is, whiskers, and β-sialon is represented by the composition formula: Si 6 −zAlzOzN 8 −z, the z value is limited to within the range of 0.2 to 3.0. As a result, they found that the resulting sialon-based sintered material has high toughness and excellent thermal shock resistance while maintaining high hardness and excellent wear resistance. Therefore, this invention was made based on the above knowledge, and contains a metal carbon/nitride dispersed phase: 2 to 30% by volume, and further contains, if necessary, the same dispersed phase forming component. Mg, Y, Al,
One of the oxides of Si, Ti, Zr, and Hf (hereinafter collectively referred to as metal oxide dispersed phase)
A species or two or more species: 1 to 20% by volume, and the remainder is a composition formula as a matrix forming component:
Si 6 −zAlzOzN 8 −z (however, 0.2≦z≦3.0) has a composition consisting of β-SiAlON and inevitable impurities, and more than 30% by volume of the carbon/nitride dispersed phase of the above metal is acicular crystals ( It is characterized by a sialon-based sintered material composed of whiskers). The acicular crystals of the metal carbon/nitride dispersed phase in the sialon-based sintered material of the present invention have a short fibrous shape, and are usually distributed in contact with each other at many points. By adjusting the direction of the acicular crystals, it is possible to impart directionality to the strength of the sialon-based sintered material itself. Next, the reason why the component composition of the sialon-based sintered material of the present invention is limited as described above will be explained. (a) Metallic carbon/nitride dispersed phase These components have the effect of improving the hardness of the material and thus the wear resistance, but if their content is less than 2% by volume, the desired durability cannot be achieved. If the content exceeds 30% by volume, the toughness of the material will deteriorate.
Its content was determined to be 2 to 30% by volume. (b) Metal oxide dispersed phase These components are uniformly dispersed in the matrix to improve sinterability, suppress grain growth, and improve the toughness and thermal shock resistance of the material. Since it has the effect of further improving the effect, it is included as necessary, but if the content is less than 1% by volume, the desired effect of improving the above effect cannot be obtained, whereas if it is contained in excess of 20% by volume, the above effect will not be improved. The content was determined to be 1 to 20% by volume because no improvement effect was obtained in the action, but rather a tendency for deterioration appeared. (c) Acicular crystals If the content is less than 30% by volume relative to the carbon/nitride dispersed phase of the metal, the desired high toughness and excellent thermal shock resistance cannot be ensured. Must be at least % capacity. In addition, if the content of the metal carbon/nitride dispersed phase in the material is relatively small, the proportion of needle crystals should be increased; If the amount is large, the proportion should be relatively reduced, thereby maintaining good sinterability and ensuring high toughness. (d) Value of z β-sialon having a composition with a z value of less than 0.2 has poor sinterability and cannot secure the desired high hardness (wear resistance);
In β-SiAlON having a composition with a value exceeding 3, the toughness of the material decreases significantly.
It was set as 3. Next, the sialon-based sintered material of the present invention will be specifically explained using examples. Example As a raw material powder, Si 3 N 4 powder with an average particle size of 1 μm for forming β-sialon, and 0.6 μm
m of Al 2 O 3 powder, and the same 1 μm of AlN powder, further having an average particle size within the range of 0.8 to 1.5 μm.
TiC powder, ZrC powder, HfC powder, NbC powder, TaC
powder, Mo2C powder, and WC powder, also from 0.8
TiN powder with an average particle size within the range of 1.5μm,
ZrN powder, HfN powder, NbN powder, TaN powder,
(Ti, Hf)C powder, (Zr,Nb,W)C powder,
(Hf, Nb) N powder and (Ti, W) CN powder,
Furthermore, all of them are needle-shaped crystals with a diameter of 1 to 4μ.
m, length: with dimensions within the range of 5 to 100 μm
TiC whiskers, ZrC whiskers, HfC whiskers, NbC whiskers, TaC whiskers, TiN whiskers, ZrN whiskers, HfN whiskers, NbN
Whiskers, TaN whiskers, and even 0.5-1.5μ
MgO powder with average particle size in the range of m, Y 2 O 3
Powder, Al 2 O 3 powder, SiO 2 powder, TiO 2 powder, ZrO 2 powder, and HfO 2 powder were prepared, and these raw material powders were blended into the compositions shown in Table 1, and then mixed in a ball mill. After mixing for an hour,
1ton/ cm2 pressure

【表】【table】

【表】 力にて圧粉体を形成し、ついでこれらの圧粉体
を、N2雰囲気中、温度:1700℃に1時間保持の
条件で焼結することによつて、実質的に配合組成
と同一の成分組成をもつた本発明焼結材料1〜18
およびいずれも針状結晶を含有しない比較焼結材
料1〜5を製造した。 ついで、この結果得られた本発明焼結材料1〜
18および比較焼結材料1〜5について、ビツカー
ス硬さおよび抗折力を測定すると共に、SNP432
(0.1mm×25゜チヤンフアーホーニング)の形状を
もつた切削チツプを切出し、 被削材:FC−25(硬さ:HB200)、 切削速度:200m/mm、 送り:0.5mm/rev、 切込み:2.0mm、 切削時間:10mm、 の条件での高送り連続切削試験を行ない、試験後
の切刃の逃げ面摩耗幅およびすくい面摩耗深さを
測定し、さらに、 被削材:SNCM−8(硬さ:HB320)の角材、 切削速度:120m/mm、 切込み:3mm、 送り:変化、 切削時間:各送り1分間、 の条件で断続切削試験を行ない、切刃に欠損が発
生した時点の送りを測定した。これらの測定結果
を第1表に合せて示した。 第1表に示される結果から、本発明焼結材料1
〜18は、いずれも高硬度および高靭性を有し、か
つ耐摩耗性および耐熱衝撃性にもすぐれているの
で、高送りや切削や断続切削ですぐれた切削性能
を発揮するのに対して、針状結晶(ホイスカー)
を含有しない比較焼結材料1〜5は、いずれも特
に靭性が低く、かつ耐熱衝撃性に劣るものである
ため、いずれの切削においても十分満足する結果
を示さないことが明らかである。 上述のように、この発明のサイアロン基焼結材
料は、高硬度および高靭性を有し、かつ耐摩耗性
および耐熱衝撃性にもすぐれているので、これら
の特性が要求される鋼や鋳鉄などの高速切削や、
特に重切削に切削工具として用いた場合は勿論の
こと、軸受や線引ダイヤなどの耐摩耗工具として
用いた場合にも長期に亘つてすぐれた性能を発揮
するのである。
[Table] By forming compacts by force and then sintering these compacts under N2 atmosphere at a temperature of 1700°C for 1 hour, the composition can be substantially changed. Sintered materials 1 to 18 of the present invention having the same composition as
Comparative sintered materials 1 to 5, none of which contained needle-like crystals, were manufactured. Next, the resulting sintered materials of the present invention 1-
18 and comparative sintered materials 1 to 5, the Vickers hardness and transverse rupture strength were measured, and SNP432
Cutting chips with the shape of (0.1 mm x 25° chamfer honing), work material: FC-25 (hardness: H B 200), cutting speed: 200 m/mm, feed: 0.5 mm/rev, A high-feed continuous cutting test was conducted under the following conditions: depth of cut: 2.0 mm, cutting time: 10 mm, and the flank wear width and rake face wear depth of the cutting edge were measured after the test. 8 (Hardness: H B 320) square material, Cutting speed: 120m/mm, Depth of cut: 3mm, Feed: Variable, Cutting time: 1 minute for each feed, Intermittent cutting test was conducted under the following conditions, and no damage occurred on the cutting edge. The feed was measured at the point in time. These measurement results are also shown in Table 1. From the results shown in Table 1, the sintered material 1 of the present invention
-18 all have high hardness and toughness, as well as excellent wear resistance and thermal shock resistance, so they exhibit excellent cutting performance in high feed, cutting, and interrupted cutting. Needle crystals (whiskers)
Comparative sintered materials 1 to 5 that do not contain any of these materials have particularly low toughness and poor thermal shock resistance, so it is clear that they do not show sufficiently satisfactory results in any cutting. As mentioned above, the sialon-based sintered material of the present invention has high hardness and toughness, and also has excellent wear resistance and thermal shock resistance, so it can be used in steel, cast iron, etc. that require these properties. high-speed cutting,
In particular, it exhibits excellent performance over a long period of time, not only when used as a cutting tool for heavy cutting, but also when used as a wear-resistant tool for bearings, wire drawing diamonds, etc.

Claims (1)

【特許請求の範囲】 1 分散相形成成分としてのTi,Zr,Hf,Nb,
Ta,Mo,およびWの炭化物および窒化物、並び
にこれらの2種以上の固溶体(以下これらを総称
して金属の炭・窒化物分散相という)のうちの1
種または2種以上:2〜30容量%、 母相形成成分としての組成式:Si6−zAlzOzN8
−z(ただし0.2≦z≦3.0)を有するβ−サイア
ロンおよび不可避不純物:残り、 からなる組成を有し、かつ上記金属の炭・窒化物
分散相のうちの30容量%以上が針状結晶(ホイス
カー)で構成されたことを特徴とする高靭性サイ
アロン基焼結材料。 2 分散相形成成分としてのTi,Zr,Hf,Nb,
Ta,Mo,およびWの炭化物および窒化物、並び
にこれらの2種以上の固溶体(以下これらを総称
して金属の炭・窒化物分散相という)のうちの1
種または2種以上:2〜30容量%、 同じく分散相形成成分としてのMg,Y,Al,
Si,Ti,Zr,およびHfの酸化物のうちの1種ま
たは2種以上:1〜20容量%、 母相形成成分としての組成式:Si6−zAlzOzN8
−z(ただし0.2≦z≦3.0)を有するβ−サイア
ロンおよび不可避不純物:残り、 からなる組成を有し、かつ上記金属の炭・窒化物
分散相のうちの30容量%以上が針状結晶(ホイス
カー)で構成されたことを特徴とする高靭性サイ
アロン基焼結材料。
[Claims] 1. Ti, Zr, Hf, Nb as dispersed phase forming components,
One of carbides and nitrides of Ta, Mo, and W, and solid solutions of two or more of these (hereinafter collectively referred to as metal carbon/nitride dispersed phase)
Species or two or more species: 2 to 30% by volume, Compositional formula as matrix forming component: Si 6 -zAlzOzN 8
-z (however, 0.2≦z≦3.0) and unavoidable impurities; A high-toughness sialon-based sintered material characterized by being composed of whiskers. 2 Ti, Zr, Hf, Nb as dispersed phase forming components,
One of carbides and nitrides of Ta, Mo, and W, and solid solutions of two or more of these (hereinafter collectively referred to as metal carbon/nitride dispersed phase)
Species or two or more species: 2 to 30% by volume, Mg, Y, Al, also as dispersed phase forming components,
One or more oxides of Si, Ti, Zr, and Hf: 1 to 20% by volume, compositional formula as a matrix forming component: Si 6 -zAlzOzN 8
-z (however, 0.2≦z≦3.0) and unavoidable impurities; A high-toughness sialon-based sintered material characterized by being composed of whiskers.
JP58020460A 1983-02-09 1983-02-09 High tenacity sialon base sintering material Granted JPS59146982A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP58020460A JPS59146982A (en) 1983-02-09 1983-02-09 High tenacity sialon base sintering material

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP58020460A JPS59146982A (en) 1983-02-09 1983-02-09 High tenacity sialon base sintering material

Publications (2)

Publication Number Publication Date
JPS59146982A JPS59146982A (en) 1984-08-23
JPS6227032B2 true JPS6227032B2 (en) 1987-06-11

Family

ID=12027688

Family Applications (1)

Application Number Title Priority Date Filing Date
JP58020460A Granted JPS59146982A (en) 1983-02-09 1983-02-09 High tenacity sialon base sintering material

Country Status (1)

Country Link
JP (1) JPS59146982A (en)

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS61291464A (en) * 1985-06-20 1986-12-22 三菱マテリアル株式会社 Beta' sialon base ceramic for cutting tool and manufacture
JP2579322B2 (en) * 1987-09-01 1997-02-05 株式会社リケン Titanium carbide / silicon carbide whisker / zirconia composite sintered body and method for producing the same
JPH01115807A (en) * 1987-10-29 1989-05-09 Kurasawa Opt Ind Co Ltd Sialon

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JPS59146982A (en) 1984-08-23

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