JP2771335B2 - Silicon nitride sintered body for cutting tools - Google Patents

Silicon nitride sintered body for cutting tools

Info

Publication number
JP2771335B2
JP2771335B2 JP2407340A JP40734090A JP2771335B2 JP 2771335 B2 JP2771335 B2 JP 2771335B2 JP 2407340 A JP2407340 A JP 2407340A JP 40734090 A JP40734090 A JP 40734090A JP 2771335 B2 JP2771335 B2 JP 2771335B2
Authority
JP
Japan
Prior art keywords
sintered body
silicon nitride
mol
oxide
rare earth
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 - Fee Related
Application number
JP2407340A
Other languages
Japanese (ja)
Other versions
JPH04209763A (en
Inventor
政宏 佐藤
祥二 高坂
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.)
Kyocera Corp
Original Assignee
Kyocera 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
Family has litigation
First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=18516948&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=JP2771335(B2) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Kyocera Corp filed Critical Kyocera Corp
Priority to JP2407340A priority Critical patent/JP2771335B2/en
Publication of JPH04209763A publication Critical patent/JPH04209763A/en
Application granted granted Critical
Publication of JP2771335B2 publication Critical patent/JP2771335B2/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

Links

Description

【発明の詳細な説明】DETAILED DESCRIPTION OF THE INVENTION

【0001】[0001]

【産業上の利用分野】本発明は、高硬度、高靭性で耐摩
耗性ならびに耐欠損性に優れ、特に鋳込み材の切削性能
に優れた切削工具用窒化珪素質焼結体に関する。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a silicon nitride sintered body for a cutting tool having high hardness, high toughness, excellent wear resistance and chipping resistance, and particularly excellent cutting performance of a cast material.

【0002】[0002]

【従来技術】従来から、窒化珪素質焼結体は、耐熱性、
耐熱衝撃性、および耐摩耗性に優れることから各種の熱
機関用構造材料の他に切削工具材料としての応用も進め
られている。
2. Description of the Related Art Conventionally, a silicon nitride sintered body has been known to have heat resistance,
Because of its excellent thermal shock resistance and abrasion resistance, application as a cutting tool material in addition to various structural materials for heat engines has been promoted.

【0003】近時、高密度の窒化珪素質焼結体を作成す
るために焼結助剤として酸化イットリウム(Y23
等の酸化物を添加しホットプレス焼成した切削工具用窒
化珪素質焼結体が特開昭55−32785号にて提案さ
れている。
Recently, yttrium oxide (Y 2 O 3 ) has been used as a sintering aid in order to produce a high-density silicon nitride sintered body.
Japanese Patent Application Laid-Open No. 55-32785 proposes a silicon nitride sintered body for a cutting tool which is obtained by adding an oxide such as above and firing by hot pressing.

【0004】また、別の方法として焼結助剤としてY2
3 および酸化アルミニウム(Al23 )を添加し、
窒素ガス中で常圧焼成することにより工具材料を得るこ
とが特開昭56−73670号にて提案されている。
As another method, Y 2 is used as a sintering aid.
O 3 and aluminum oxide (Al 2 O 3 ) are added,
Japanese Patent Application Laid-Open No. 56-73670 proposes obtaining a tool material by baking at normal pressure in nitrogen gas.

【0005】[0005]

【発明が解決しようとする問題点】しかしながら、焼結
助剤としてY23 を用いた場合には、室温から切削時
の高温までの強度が不十分であり、実用的なレベルに達
しておらず、さらに焼結体中にスポットと呼ばれるシミ
が発生し、耐欠損性に劣るとともに複雑形状の切削工具
を作成す場合、高価なホットプレス法を用いなければな
らないという問題がある。
THE INVENTION Problems to be Solved] However, in the case of using Y 2 O 3 as a sintering aid is insufficient strength to a high temperature during cutting from room reached a practical level In addition, spots called spots are generated in the sintered body, and there is a problem that when a cutting tool having poor fracture resistance and a complicated shape is produced, an expensive hot press method must be used.

【0006】また、特開昭56−73670号にて提案
された方法によれば、窒素ガス中で常圧焼成することか
ら複雑形状品も廉価に作成することができるが、焼結助
剤としてY23 およびAl23 を用いる系では焼結
体の破壊靭性が低下するためにやはり耐欠損性に劣ると
いう欠点を有している。
According to the method proposed in Japanese Patent Application Laid-Open No. 56-73670, complicated shaped articles can be produced at low cost by baking at normal pressure in nitrogen gas. A system using Y 2 O 3 and Al 2 O 3 also has a disadvantage that the fracture toughness of the sintered body is lowered, so that the fracture resistance is also poor.

【0007】[0007]

【問題点を解決するための手段】本発明者等は、上記の
問題点に対して検討を重ねた結果、窒化珪素に対する焼
結助剤としてY23 以外の特定の希土類元素酸化物を
添加するとともに焼結体中に含まれる過剰酸素分の量を
調整するとともに、これらの焼結助剤を特定に比率で含
有させることにより、常圧焼成による緻密化が可能であ
り、且つ硬度、強度、耐摩耗性ならびに耐欠損性に優れ
た切削工具用として適した焼結体が得られることを知見
した。
[Means for Solving the Problems] The present inventors have studied the above problems and found that a specific rare earth element oxide other than Y 2 O 3 was used as a sintering aid for silicon nitride. By adding and adjusting the amount of excess oxygen contained in the sintered body, and by including these sintering aids in a specific ratio, densification by normal pressure firing is possible, and hardness, It has been found that a sintered body suitable for a cutting tool having excellent strength, wear resistance and fracture resistance can be obtained.

【0008】即ち、本発明の切削工具用窒化珪素質焼結
体は、窒化珪素が85〜99モル%と、Er、Yb、S
c、DyおよびHoから選ばれる少なくとも1種の希土
類元素が酸化物換算で0.5〜5モル%と、過剰酸素が
SiO2 換算して10モル%以下の割合からなる焼結体
であって、前記過剰酸素の前記希土類元素の酸化物換算
量に対するモル比が0.5〜2.5であり、且つビッカ
ース硬度が14.5GPa以上であることを特徴とする
ものである。
That is, the silicon nitride sintered body for a cutting tool of the present invention contains 85 to 99 mol% of silicon nitride, Er, Yb, S
A sintered body comprising at least one rare earth element selected from c, Dy and Ho in a proportion of 0.5 to 5 mol% in terms of oxide and excess oxygen in a proportion of 10 mol% or less as SiO 2. The molar ratio of the excess oxygen to the amount of the rare earth element in terms of oxide is 0.5 to 2.5, and the Vickers hardness is 14.5 GPa or more.

【0009】本発明によれば、まず、焼結体の組成が、
窒化珪素が85〜99モル%、特に88〜97モル%、
希土類元素としてEr、Yb、Sc、DyおよびHoか
ら選ばれる少なくとも1種を選択し、この元素の酸化物
換算量(単にRE23 と称する場合もある)が0.5〜
5モル%、特に、2〜4モル%、また過剰酸素のSiO
2 換算量(単にSiO2 と称する場合もある)が10モ
ル%以下の割合からなることが重要である。
According to the present invention, first, the composition of the sintered body is
85-99 mol% of silicon nitride, especially 88-97 mol%,
At least one selected from Er, Yb, Sc, Dy and Ho is selected as the rare earth element, and the oxide equivalent amount of this element (sometimes simply referred to as RE 2 O 3 ) is 0.5 to 0.5.
5 mol%, especially 2-4 mol%, and excess oxygen of SiO
It is important that the 2 conversion amount (sometimes simply referred to as SiO 2 ) be 10 mol% or less.

【0010】なお、過剰酸素とは、焼結体全体に含まれ
る全酸素量からSiO2 を除く焼結助剤として窒化珪素
に添加された成分中に含まれる酸素を除いた残りの酸素
量で、具体的には窒化珪素粉末中に不可避的に含まれる
不純物酸素あるいはSiO2 として添加された酸素から
構成されるものである。
[0010] The excess oxygen is the amount of oxygen remaining after removing the oxygen contained in the component added to silicon nitride as a sintering aid excluding SiO 2 from the total oxygen content contained in the entire sintered body. Specifically, it is composed of impurity oxygen inevitably contained in the silicon nitride powder or oxygen added as SiO 2 .

【0011】ここで焼結体の組成を上記の範囲に設定し
たのは、窒化珪素が85モル%より少なく、あるいは希
土類元素の酸化物換算量が5モル%より多いと焼結体の
硬度が低下し工具としての耐摩耗性が劣化し、窒化珪素
が99モル%より多く、あるいは希土類元素の酸化物換
算量が0.5モル%より少ないと緻密体が得られずに焼結
体の強度自体が低下するからである。一方、過剰酸素量
が10モル%より多いと、靭性が低下し工具としての耐
欠損性が劣化する。
The reason why the composition of the sintered body is set in the above range is that the hardness of the sintered body is reduced when the content of silicon nitride is less than 85% by mole or the amount of rare earth element in terms of oxide is more than 5% by mole. If the wear resistance as a tool deteriorates, the content of silicon nitride is more than 99 mol%, or the amount of rare earth element as oxide is less than 0.5 mol%, a dense body cannot be obtained, and the strength of the sintered body is not obtained. This is because the material itself is reduced. On the other hand, if the excess oxygen amount is more than 10 mol%, the toughness is reduced and the fracture resistance as a tool is deteriorated.

【0012】また、本発明によれば、上記の組成におい
て過剰酸素と希土類元素との(SiO2 /RE23
で表されるモル比が0.5〜2.5、特に1〜1.8であるこ
とも重要である。これはこのモル比が0.5より小さいと
緻密な焼結体が得られず、2.5より大きいと靭性が低下
し耐欠損性が劣化するからである。
Further, according to the present invention, in the above-mentioned composition, (SiO 2 / RE 2 O 3 )
It is also important that the molar ratio represented by is 0.5 to 2.5, especially 1 to 1.8. This is because if the molar ratio is less than 0.5, a dense sintered body cannot be obtained, and if the molar ratio is more than 2.5, toughness is reduced and fracture resistance is deteriorated.

【0013】なお、本発明の焼結体は、切削工具として
の耐摩耗性、耐欠損性の点から考慮してAl23 やM
gO等の酸化物はできるだけ存在しないことが望まし
く、具体的には1重量%以下に制御することが望まし
い。
The sintered body of the present invention is made of Al 2 O 3 or M 2 in consideration of wear resistance and fracture resistance as a cutting tool.
It is desirable that oxides such as gO do not exist as much as possible. Specifically, it is desirable to control the content to 1% by weight or less.

【0014】次に、本発明の窒化珪素質焼結体を製造す
る方法について説明すると、まず、原料粉末として、窒
化珪素粉末およびEr23 、Yb23 、Sc2
3 、Dy23 およびHo23 から選ばれる少なくと
も1種の酸化物粉末、場合によってSiO2 粉末を準備
する。
Next, the method for producing the silicon nitride sintered body of the present invention will be described. First, silicon nitride powder and Er 2 O 3 , Yb 2 O 3 , Sc 2 O are used as raw material powders.
3, at least one oxide powders selected from Dy 2 O 3 and Ho 2 O 3, to prepare a SiO 2 powder as the case may be.

【0015】なお、窒化珪素粉末としてはα型、β型の
2種が知られているが、焼結性を促進するためにα−S
34 が90%以上であることが望ましく、また、不
純物酸素量0.8〜1.5重量%、BET比表面積が3〜2
0m2 であることがよい。
[0015] It should be noted that two types of silicon nitride powder, α-type and β-type, are known, but α-S
i 3 N 4 is desirably 90% or more, the impurity oxygen amount is 0.8 to 1.5% by weight, and the BET specific surface area is 3 to 2%.
It is preferably 0 m 2 .

【0016】次にこれらの原料粉末を前述した組成とな
るように秤量混合し、これに適宜バインダーを添加して
造粒後、公知の成形方法、例えばプレス成形法、押出成
形法、射出成形法あるいは鋳込み成形法等の成形法で所
望の形状に成形し、その後焼成する。
Next, these raw material powders are weighed and mixed so as to have the above-described composition, a binder is appropriately added thereto, and the mixture is granulated. Then, a known molding method such as a press molding method, an extrusion molding method, or an injection molding method is used. Alternatively, it is formed into a desired shape by a molding method such as a casting method, and then fired.

【0017】焼成手段としては公知の方法が採用される
が、本発明における1つの特徴としては、前述したよう
な組成にすることにより、機械的な圧力なしに窒素ガス
圧力1〜100気圧の雰囲気にて1700〜2000℃
の焼成温度で焼成することにより対理論密度比95%以
上の緻密な焼結体を得ることができる。それにより、こ
れまで一般に採用されていたホットプレス法に比較して
より安価に製造することができる。また、場合により上
記焼成後にさらに熱間静水圧焼成によりさらに緻密化す
ることもできる。
As the firing means, a known method is employed. One feature of the present invention is that the composition as described above allows the atmosphere having a nitrogen gas pressure of 1 to 100 atm without mechanical pressure. 1700-2000 ℃
By firing at the firing temperature described above, a dense sintered body having a theoretical density ratio of 95% or more can be obtained. Thereby, it can be manufactured at a lower cost as compared with the hot press method generally used until now. Further, in some cases, it is possible to further densify by hot isostatic pressing after the above-mentioned firing.

【0018】[0018]

【実施例】原料粉末として、窒化珪素粉末(BET比表
面積15m2 /g、α化率95%、不純物酸素量0.9
重量%)と、表1に示した各希土類元素酸化物粉末、酸
化珪素粉末を用いて最終焼結体組成が表1の組成になる
ようにバインダーとともに調合混合し、1t/cm2
圧力でプレス成形し、工具形状SNGN120412用
の成形体を得た。
EXAMPLE As a raw material powder, silicon nitride powder (BET specific surface area 15 m 2 / g, pregelatinization rate 95%, impurity oxygen amount 0.9
% By weight) and the respective rare earth oxide powders and silicon oxide powders shown in Table 1 were mixed and mixed with a binder so that the final sintered body composition became the composition shown in Table 1, and the pressure was 1 t / cm 2 . Press molding was performed to obtain a molded body for a tool shape SNGN120412.

【0019】この成形体を脱脂後、1900℃で3時
間、窒素ガス圧力30気圧下で焼成し、得られた焼結体
においてアルキメデス法により焼結体の密度を測定する
とともに、ビッカース硬度及びIF法により破壊靭性を
求めた。
After degreased, the compact was fired at 1900 ° C. for 3 hours under a nitrogen gas pressure of 30 atm. The density of the obtained sintered body was measured by Archimedes method, and the Vickers hardness and IF were measured. The fracture toughness was determined by the method.

【0020】さらに、工具形状に研磨後、下記の条件 被削材 FC−25 切削速度 400m/min 送り 0.2mm/rev 切り込み 2.0mm 切削試験を行い、刃先のフランク摩耗量が0.2mmにな
るまでの時間を測定し、結果を表1に示した。
Further, after polishing to a tool shape, the following conditions were applied. Work material FC-25 Cutting speed 400 m / min Feed 0.2 mm / rev Depth of cut 2.0 mm A cutting test was performed to reduce the flank wear of the cutting edge to 0.2 mm. The time until the time was reached was measured, and the results are shown in Table 1.

【0021】[0021]

【表1】 [Table 1]

【0022】表1によれば、本発明の試料はいずれも硬
度14.5GPa、靭性6.9MPa・m1/2 以上の優れた
特性を示し、切削テストにおいても優れた切削性能を示
した。
According to Table 1, all of the samples of the present invention exhibited excellent properties of hardness of 14.5 GPa and toughness of 6.9 MPa · m 1/2 or more, and also exhibited excellent cutting performance in a cutting test.

【0023】これに対して、Y23 を用いた試料No
10,11は、硬度、靭性値はある程度高い値を示した
が、切削テストにおいてチッピングによる異常摩耗を示
した。また、希土類元素酸化物量が5モル%を越える試
料No,12、過剰酸素量が10モル%を越える試料No,
13、希土類元素酸化物と過剰酸素との比率が0.5より
小さい試料No,14および比率が2.5を越える試料No,
15は、いずれも本発明品と比較して硬度、靭性が低
く、切削テストにおいても劣るものであった。
On the other hand, the sample No. using Y 2 O 3
Samples Nos. 10 and 11 showed high hardness and toughness values, but showed abnormal wear due to chipping in the cutting test. Further, Sample No. 12 in which the amount of rare earth element oxide exceeds 5 mol%, and Sample No. 12 in which the excess oxygen amount exceeds 10 mol%.
13. Samples No. 14 and 14 in which the ratio between the rare earth oxide and excess oxygen is smaller than 0.5 and samples No. and 14 in which the ratio exceeds 2.5.
No. 15 was lower in hardness and toughness as compared with the product of the present invention, and was inferior in the cutting test.

【0024】[0024]

【発明の効果】以上詳述した通り、本発明の切削工具用
窒化珪素質焼結体は、窒化珪素に対して特定の希土類元
素を過剰酸素と特定の割合からなるように含有させるこ
とにより、これまでにない優れた硬度と靭性を付与する
ことができることから、切削工具としても切削特性を向
上できるとともに工具の寿命を延ばすことができる。
As described above in detail, the silicon nitride sintered body for a cutting tool of the present invention contains a specific rare earth element with respect to silicon nitride so as to be composed of excess oxygen and a specific ratio. Since excellent hardness and toughness, which have never been achieved before, can be imparted, cutting characteristics can be improved as a cutting tool and the life of the tool can be extended.

フロントページの続き (58)調査した分野(Int.Cl.6,DB名) C04B 35/584 B23B 27/14Continuation of front page (58) Field surveyed (Int.Cl. 6 , DB name) C04B 35/584 B23B 27/14

Claims (1)

(57)【特許請求の範囲】(57) [Claims] 【請求項1】窒化珪素が85〜99モル%と、Er、Y
b、Sc、DyおよびHoから選ばれる少なくとも1種
の希土類元素が酸化物換算で0.5〜5モル%と、過剰
酸素がSiO2 換算して10モル%以下の割合からなる
焼結体であって、前記過剰酸素の前記希土類元素の酸化
物換算量に対するモル比が0.5〜2.5であり、且つ
ビッカース硬度が14.5GPa以上であることを特徴
とする切削工具用窒化珪素質焼結体。
1. The method according to claim 1, wherein 85 to 99 mol% of silicon nitride and Er, Y
A sintered body in which at least one rare earth element selected from b, Sc, Dy and Ho has a ratio of 0.5 to 5 mol% in terms of oxide and excess oxygen has a ratio of 10 mol% or less in terms of SiO 2. Wherein the molar ratio of the excess oxygen to the oxide equivalent of the rare earth element is 0.5 to 2.5, and the Vickers hardness is 14.5 GPa or more. Sintered body.
JP2407340A 1990-12-07 1990-12-07 Silicon nitride sintered body for cutting tools Expired - Fee Related JP2771335B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP2407340A JP2771335B2 (en) 1990-12-07 1990-12-07 Silicon nitride sintered body for cutting tools

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP2407340A JP2771335B2 (en) 1990-12-07 1990-12-07 Silicon nitride sintered body for cutting tools

Publications (2)

Publication Number Publication Date
JPH04209763A JPH04209763A (en) 1992-07-31
JP2771335B2 true JP2771335B2 (en) 1998-07-02

Family

ID=18516948

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2407340A Expired - Fee Related JP2771335B2 (en) 1990-12-07 1990-12-07 Silicon nitride sintered body for cutting tools

Country Status (1)

Country Link
JP (1) JP2771335B2 (en)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH08300205A (en) 1995-05-09 1996-11-19 Mitsubishi Materials Corp Cutting tool made of silicon nitride sintered material excellent in chipping resisting property

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS55116672A (en) * 1979-02-27 1980-09-08 Tokyo Shibaura Electric Co Manufacture of heat resisting high strength sintered body
JPS63112468A (en) * 1986-10-29 1988-05-17 日産自動車株式会社 Manufacture of silicon nitride base sintered body
JP2631108B2 (en) * 1987-09-30 1997-07-16 京セラ株式会社 Manufacturing method of silicon nitride sintered body
JP2742596B2 (en) * 1988-02-29 1998-04-22 京セラ株式会社 Silicon nitride sintered body and method for producing the same

Also Published As

Publication number Publication date
JPH04209763A (en) 1992-07-31

Similar Documents

Publication Publication Date Title
JP3588162B2 (en) Silicon nitride cutting tool and method of manufacturing the same
JP2771335B2 (en) Silicon nitride sintered body for cutting tools
JP2851721B2 (en) Silicon nitride sintered body for cutting tools
JP3426823B2 (en) Silicon nitride sintered body and method for producing the same
JP3454993B2 (en) Silicon nitride sintered body and method for producing the same
JP3034100B2 (en) Silicon nitride sintered body and method for producing the same
JP3124865B2 (en) Silicon nitride sintered body and method for producing the same
JP2980342B2 (en) Ceramic sintered body
JPH1029869A (en) Silicon nitride-silicon carbide composite sintered compact and its production
JPH09157028A (en) Silicon nitride sintered compact and its production
JPH07267738A (en) Wear resistant silicon nitride sintered compact and its production
JP2892186B2 (en) Method for producing silicon nitride-silicon carbide composite sintered body
JP2710865B2 (en) Manufacturing method of silicon nitride sintered body
JP2631108B2 (en) Manufacturing method of silicon nitride sintered body
JP3445345B2 (en) High heat-resistant water sialon-based sintered body
JP2631102B2 (en) Method for producing silicon nitride based sintered body
JPH10279360A (en) Silicon nitride structural parts and its production
JP3124864B2 (en) Silicon nitride sintered body and method for producing the same
JPH10212167A (en) Silicon nitride-base composite sintered compact and its production
JP2592267B2 (en) Sialon reinforced with silicon carbide whiskers
JP2708136B2 (en) Silicon nitride sintered body and method for producing the same
EP0317147B1 (en) Si3n4-al2o3 composite sintered bodies and method of producing the same
JP3124862B2 (en) Method for producing silicon nitride based sintered body
JP3591799B2 (en) High toughness silicon nitride based sintered body and method for producing the same
JP2801447B2 (en) Method for producing silicon nitride based sintered body

Legal Events

Date Code Title Description
FPAY Renewal fee payment (event date is renewal date of database)

Free format text: PAYMENT UNTIL: 20080417

Year of fee payment: 10

FPAY Renewal fee payment (event date is renewal date of database)

Free format text: PAYMENT UNTIL: 20090417

Year of fee payment: 11

FPAY Renewal fee payment (event date is renewal date of database)

Free format text: PAYMENT UNTIL: 20090417

Year of fee payment: 11

FPAY Renewal fee payment (event date is renewal date of database)

Free format text: PAYMENT UNTIL: 20100417

Year of fee payment: 12

LAPS Cancellation because of no payment of annual fees