Deprecated: The each() function is deprecated. This message will be suppressed on further calls in /home/zhenxiangba/zhenxiangba.com/public_html/phproxy-improved-master/index.php on line 456
JPS5927744B2 - High toughness ceramic cutting tools - Google Patents
[go: Go Back, main page]

JPS5927744B2 - High toughness ceramic cutting tools - Google Patents

High toughness ceramic cutting tools

Info

Publication number
JPS5927744B2
JPS5927744B2 JP54140352A JP14035279A JPS5927744B2 JP S5927744 B2 JPS5927744 B2 JP S5927744B2 JP 54140352 A JP54140352 A JP 54140352A JP 14035279 A JP14035279 A JP 14035279A JP S5927744 B2 JPS5927744 B2 JP S5927744B2
Authority
JP
Japan
Prior art keywords
volume
powder
ceramic cutting
alumina
toughness ceramic
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
JP54140352A
Other languages
Japanese (ja)
Other versions
JPS5663870A (en
Inventor
宏秀 山田
賢司 長谷川
久雄 原
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.)
Proterial Ltd
Original Assignee
Hitachi Metals Ltd
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 Hitachi Metals Ltd filed Critical Hitachi Metals Ltd
Priority to JP54140352A priority Critical patent/JPS5927744B2/en
Publication of JPS5663870A publication Critical patent/JPS5663870A/en
Publication of JPS5927744B2 publication Critical patent/JPS5927744B2/en
Expired legal-status Critical Current

Links

Landscapes

  • Compositions Of Oxide Ceramics (AREA)

Description

【発明の詳細な説明】 本発明は、特に靭性にすぐれ、しかも耐熱衝撃による耐
欠損性にすぐれた高硬度材料の旋削加工、鋳鉄材料のフ
ライス加工等の用途に適した切削工具用材料に関するも
のである。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a material for cutting tools that has particularly excellent toughness and excellent fracture resistance due to thermal shock resistance and is suitable for applications such as turning of high-hardness materials and milling of cast iron materials. It is.

現在市販されているセラミック切削工具を大別するとア
ルミナセラミックとアルミナ−炭化チタン系セラミック
の2種類がある。
Ceramic cutting tools currently on the market can be roughly divided into two types: alumina ceramics and alumina-titanium carbide ceramics.

アルミナセラミックは、アルミナ固有の特徴である高温
かつ酸化性雰囲気下での耐摩耗性のすぐれた点を利用し
て刃先温度が1200℃を越える切削条件になる、鋳鉄
材料の超高速仕上旋削加工にはなくてはならない存在で
ある。
Alumina ceramic is suitable for ultra-high-speed finishing turning of cast iron materials, where the cutting edge temperature exceeds 1200°C, by taking advantage of the unique characteristics of alumina, which is its excellent wear resistance under high temperatures and oxidizing atmospheres. It is an indispensable existence.

しかし、アルミナセラミックは靭性が不足であることと
、熱衝撃による耐欠損性に問題があるため高硬度材料の
旋削加工、鋳鉄材料のフライス加工および湿式旋削加工
に使用することは不適当である。一方、アルミナ−炭化
チタン系セラミックスは、アルミナに約30重量%のT
iOを複合化して、結晶粒を微細化すると同時にアルミ
ナ固有の性質である高温になる程熱伝導度が低下する欠
点を補つて、熱衝撃による耐欠損性を改善した材料であ
る。
However, alumina ceramics are unsuitable for use in turning high-hardness materials, milling cast iron materials, and wet turning because they lack toughness and have problems with fracture resistance due to thermal shock. On the other hand, alumina-titanium carbide ceramics contain approximately 30% by weight of T in alumina.
It is a material that improves fracture resistance due to thermal shock by compounding iO to make the crystal grains finer and at the same time compensate for the inherent characteristic of alumina, which is that the thermal conductivity decreases as the temperature increases.

この材料は難焼結性であるためホットプレス焼結法が採
用されていることもあり、微細な複合組織を有するとと
もに、高い硬度および靭性をもち、抗折力も80〜90
〜/mTn2とすぐれているため、アルミナセラミック
では不適当であつた鋳鉄材料のフライス加工および湿式
旋削加工にも使用されている。本発明者は、生産性の悪
いホットプレス法によらず熱間静水圧プレス(以下HI
Pと示す)法に適したAe2O3−(窒化物、硼化物)
系セラミツク工具の研究を行つた結果、TiCの高温で
の硬さ、熱伝導度に匹敵し、しかもTlCより耐酸化性
にすぐれたTiB2がAl2O3−TiC系よりも焼結
性が良いため、HIP法が適用でき、Al2O3−Ti
C系に匹適するセラミツク工具を開発することができた
Because this material is difficult to sinter, the hot press sintering method is used, and it has a fine composite structure, high hardness and toughness, and a transverse rupture strength of 80 to 90.
Because of its excellent value of ~/mTn2, it is also used for milling and wet turning of cast iron materials, for which alumina ceramics are unsuitable. The present inventor has developed a method using hot isostatic pressing (hereinafter referred to as HI) without using the hot pressing method, which has poor productivity.
Ae2O3- (nitride, boride) suitable for the method (denoted as P)
As a result of research on HIP-based ceramic tools, TiB2, which has comparable high-temperature hardness and thermal conductivity to TiC and has better oxidation resistance than TlC, has better sinterability than Al2O3-TiC. method can be applied, and Al2O3-Ti
We were able to develop a ceramic tool that is comparable to the C series.

しかしながら、Al2O3−TiB2系をHIP処理す
るためには予備焼結で相対密度9501,以上にする必
要があり、例えば真空焼結では1500℃以上で焼結す
る必要があるため、結晶粒の粗大化が避けられなかつた
。そこで、本発明者らはAl2O3−TiB2系の結晶
粒を微細にするための種々の添加物を検討した結果AI
Nが、焼結性を著しく阻害せずに、結晶粒を微細化する
効果のあることが判明した。
However, in order to HIP the Al2O3-TiB2 system, it is necessary to achieve a relative density of 9501 or higher through preliminary sintering, and for example, in vacuum sintering, it is necessary to sinter at a temperature of 1500°C or higher, resulting in coarse grains. was unavoidable. Therefore, the present inventors investigated various additives to make Al2O3-TiB2-based crystal grains fine and found that AI
It has been found that N has the effect of refining crystal grains without significantly inhibiting sinterability.

Al2O3一TiB2系にAINを配合したセラミツク
スの焼結体の結晶粒度はAINを配合しないセラミツク
スの焼結体の結晶粒度より著しく微細にできたため、靭
性が向上し、耐欠損性を改善することができる。本発明
は、上記知見に基づいてなされたものであり、αAl2
O3粉末を主成分としてTlB2粉末5〜15体積%A
IN粉末0.2〜2.0体積%からなることを特徴とす
る高靭性セラミツク切削工具である。また、本発明にお
いて体積%で0.05〜1.5%のMgOを含有しても
よく、さらに体積?で0.05〜1.5%のNlO,C
r2O3,TiO,TiO2,Y2O3を複合添加した
ものでも同様な効果が得られる。また本発明のセラミツ
クは上記組成範囲の混合粉末を、一担予備焼結を行つた
後、HIPすることによつて得ることができた。本発明
のセラミツタスにおいて、TiB2粉末を5〜15体積
%に限定した理由は、5体積%以下の場合、黒色セラミ
ツクとしての特徴がなくなるためであり、15体積%以
上になると、焼結性が著しく悪化するためTlB2粉末
は5〜15体積%に限定した。
The grain size of the ceramic sintered body in which AIN is blended with the Al2O3-TiB2 system is significantly finer than that of the ceramic sintered body that does not contain AIN, resulting in improved toughness and fracture resistance. can. The present invention was made based on the above findings, and αAl2
TlB2 powder 5-15% by volume A with O3 powder as the main component
This is a high toughness ceramic cutting tool characterized by comprising 0.2 to 2.0 volume % of IN powder. Further, in the present invention, MgO may be contained in an amount of 0.05 to 1.5% by volume, and further may contain MgO of 0.05 to 1.5% by volume. 0.05-1.5% NlO,C
A similar effect can be obtained by adding r2O3, TiO, TiO2, and Y2O3 in combination. The ceramic of the present invention could be obtained by pre-sintering a mixed powder having the above-mentioned composition range, followed by HIPing. The reason why TiB2 powder is limited to 5 to 15% by volume in the ceramics of the present invention is that if it is less than 5% by volume, it will lose its characteristics as a black ceramic, and if it is more than 15% by volume, the sinterability will be significantly reduced. TlB2 powder was limited to 5 to 15% by volume to avoid deterioration.

AIN末は0.2体積%以下になると結晶粒微細化の効
果がなくなり、2.0体積%以上になると焼結性が著し
く悪化するので、AIN粉末は0.2〜2.0体積%に
限定した。MgO粉末は0.05体積%以下では、アル
ミナ結晶粒微細化の効果がなく、1.5体積%以上にな
るとアルミナと反応して結晶粒界にスピネル層が生じて
脆化するため、MgO粉末は0.05〜1.5体積%と
した。また、本発明において、NiO,Cr2O3,T
iO,TlO2,Y2O3のうちの1種または2種以上
を添加した場合にも結晶粒微細化の効果が得られるが、
0.05体積%未満ではアルミナ結晶粒微細化の効果が
なく、一方、1.5体積%を越えると結晶粒界に異相が
生じて脆化するため、これら成分の添加量は総量で0,
05〜1.5体積%の範囲内とすることが望ましい。本
発明においては、TiB2の一部を2体積%以下の周期
律表1va,va,v1a族の窒化物、硼化物およびB
N,Si3N4で置換しても同様の効果が得られた。
When the amount of AIN powder is less than 0.2 volume%, the grain refining effect disappears, and when it is more than 2.0 volume%, the sinterability deteriorates significantly, so the amount of AIN powder is 0.2 to 2.0 volume%. Limited. If MgO powder is less than 0.05 volume%, it has no effect on refining alumina crystal grains, and if it is more than 1.5 volume%, it reacts with alumina and forms a spinel layer at the grain boundaries, resulting in embrittlement. was set at 0.05 to 1.5% by volume. Furthermore, in the present invention, NiO, Cr2O3, T
The effect of grain refinement can also be obtained when one or more of iO, TlO2, Y2O3 is added.
If it is less than 0.05 volume %, there is no effect on refining alumina crystal grains, while if it exceeds 1.5 volume %, different phases will occur at the grain boundaries and embrittlement will occur. Therefore, the total amount of these components added is 0.
It is desirable that the content be within the range of 0.05 to 1.5% by volume. In the present invention, a part of TiB2 is 2% by volume or less of nitrides, borides, and B of groups 1va, va, and v1a of the periodic table.
A similar effect was obtained by substituting N, Si3N4.

以下実施例に基づき詳細に説明する。A detailed explanation will be given below based on examples.

平均粒径0.1μ、純度99.9%のαAl2O3,T
iB2および結晶粒微細化の効果を検討するためにMg
Oおよびその他の酸化物を第1表に示すような割合で配
合しエチルアルコールを使用して、アルミナ製のボール
ミルで湿式混合を行つた。
αAl2O3,T with average particle size 0.1μ and purity 99.9%
Mg was used to examine the effects of iB2 and grain refinement.
O and other oxides were blended in the proportions shown in Table 1 and wet mixed using ethyl alcohol in an alumina ball mill.

混合後、真空乾燥し、造粒後2t/(:Tnで成形した
。成形体は1500−1550℃で2時間、10−2T
0rrの真空中で焼結した。焼結体は1450℃、10
00気圧で1時間HIP処理を行つた。
After mixing, vacuum drying, granulation and molding with 2T/(:Tn).
Sintering was carried out in a vacuum of 0 rr. The sintered body was heated at 1450℃, 10
HIP treatment was performed for 1 hour at 0.00 atm.

得られた焼結体の硬さ、抗折強度および相対密度を第1
表に示す。第1表より、Al2O3−TiB2系では、
AINを0.5〜2.0体積%添加した材料はいずれも
抗折強度が90K9/ml以上であり、第1表の他の材
料と比較して、著しく抗折強度が改善されている。
The hardness, bending strength and relative density of the obtained sintered body were
Shown in the table. From Table 1, in the Al2O3-TiB2 system,
All of the materials to which AIN was added in an amount of 0.5 to 2.0 volume % had a transverse strength of 90K9/ml or more, and the transverse strength was significantly improved compared to the other materials in Table 1.

なお、AIN5.O体積%配合の場合は、真空焼結で、
相対密度が95%以下であるため、HIP処理の効果が
現われなかつた。第1図及至第4図は、結晶組織に及ぼ
す、AIN添加の効果を示す走査型電子顕微鏡写真であ
る第1図は体積比で93.0A1203−5TiB2−
1.0AIN一1.0Mg0材の第2図は94.7A1
203−5TiB2一0.3Mg0材の、第3図は93
.9A1203−5TiB2一1.0B203−0.1
Mg0材の、第4図は93.8A1203−5TiB2
−1.0Ni0−0.2Mg0材の各組織を示す。
In addition, AIN5. In case of O volume% combination, vacuum sintering
Since the relative density was 95% or less, the effect of HIP treatment was not apparent. Figures 1 to 4 are scanning electron micrographs showing the effect of AIN addition on the crystal structure. Figure 1 shows a volume ratio of 93.0A1203-5TiB2-
The second figure for 1.0AIN-1.0Mg0 material is 94.7A1.
203-5TiB2-0.3Mg0 material, Figure 3 is 93
.. 9A1203-5TiB2-1.0B203-0.1
The Mg0 material in Figure 4 is 93.8A1203-5TiB2.
Each structure of the -1.0Ni0-0.2Mg0 material is shown.

図から他の添加物と比較AINの添加は、結晶粒微細化
に著しく効果のあることが明らかである。上述のように
、本発明のセラミツクは、結晶粒の微細化により、すぐ
れた靭性を有し、Al2O3−TiO系よりも耐酸化性
のすぐれたセラミツクであり、切削工具として使用した
場合、鋳鉄材料のフライス加工にすぐれた切削特性が期
待できる。
It is clear from the figure that the addition of AIN compared with other additives has a remarkable effect on grain refinement. As mentioned above, the ceramic of the present invention has excellent toughness due to the refinement of crystal grains, and is a ceramic that has better oxidation resistance than Al2O3-TiO type ceramics, and when used as a cutting tool, it can be used as a cutting tool for cast iron materials. Excellent cutting characteristics can be expected for milling.

【図面の簡単な説明】[Brief explanation of drawings]

第1図及至第4図はAl2O3−TiB2系の結晶粒微
細化にAINが効果あることを示すための破面の走査型
電子顕微鏡写真である。
FIGS. 1 to 4 are scanning electron micrographs of fractured surfaces showing that AIN is effective in refining Al2O3-TiB2-based crystal grains.

Claims (1)

【特許請求の範囲】 1 αAl_2O_3粉末を主成分として、TiB_2
粉末5〜15体積%、AlN粉末0.2〜2.0体積%
からなることを特徴とする高靭性セラミック切削工具。 2 特許請求の範囲第1項記載のものにおいて、副成分
として、0.05〜1.5体積%のMgOを添加含有し
たことを特徴とする高靭性セラミック切削工具。 3 αAl_2O_3粉末を主成分として、TiB_2
粉末5〜15体積%、AlN粉末0.2〜2.0体積%
、およびNiO、Cr_2O_3、B_2O_3、Ti
O、TiO_2、Y_2O_3のうちの1種または2種
以上0.05〜1.5体積%からなることを特徴とする
高靭性セラミック切削工具。 4 特許請求の範囲第3項記載のものにおいて、副成分
として、0.05〜1.5体積%のMgOを添加含有し
たことを特徴とする高靭性セラミック切削工具。
[Claims] 1 TiB_2 with αAl_2O_3 powder as the main component
Powder 5-15 volume%, AlN powder 0.2-2.0 volume%
A high-toughness ceramic cutting tool characterized by comprising: 2. A high-toughness ceramic cutting tool according to claim 1, characterized in that 0.05 to 1.5% by volume of MgO is added as a subcomponent. 3 With αAl_2O_3 powder as the main component, TiB_2
Powder 5-15 volume%, AlN powder 0.2-2.0 volume%
, and NiO, Cr_2O_3, B_2O_3, Ti
A high-toughness ceramic cutting tool comprising 0.05 to 1.5 volume % of one or more of O, TiO_2, and Y_2O_3. 4. A high-toughness ceramic cutting tool according to claim 3, characterized in that 0.05 to 1.5% by volume of MgO is added as a subcomponent.
JP54140352A 1979-10-30 1979-10-30 High toughness ceramic cutting tools Expired JPS5927744B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP54140352A JPS5927744B2 (en) 1979-10-30 1979-10-30 High toughness ceramic cutting tools

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP54140352A JPS5927744B2 (en) 1979-10-30 1979-10-30 High toughness ceramic cutting tools

Publications (2)

Publication Number Publication Date
JPS5663870A JPS5663870A (en) 1981-05-30
JPS5927744B2 true JPS5927744B2 (en) 1984-07-07

Family

ID=15266825

Family Applications (1)

Application Number Title Priority Date Filing Date
JP54140352A Expired JPS5927744B2 (en) 1979-10-30 1979-10-30 High toughness ceramic cutting tools

Country Status (1)

Country Link
JP (1) JPS5927744B2 (en)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS61232267A (en) * 1985-04-08 1986-10-16 ニツコ−株式会社 Manufacture of high strength alumina green

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5122002A (en) * 1974-08-20 1976-02-21 Takeshi Abiru BURASHIHORUDA
GB1498158A (en) * 1975-01-15 1978-01-18 Activite Atom Avance Insulating refractory products having high porosity and their method of preparation
DE2741295C2 (en) * 1977-09-14 1989-12-14 Fried. Krupp Gmbh, 4300 Essen Ceramic molded body

Also Published As

Publication number Publication date
JPS5663870A (en) 1981-05-30

Similar Documents

Publication Publication Date Title
US4543343A (en) Ceramics for cutting tools
EP0347920B1 (en) High strength high toughness TiB2 ceramics
EP0170889B1 (en) Zrb2 composite sintered material
US4396724A (en) Ceramic composition
JPS5927744B2 (en) High toughness ceramic cutting tools
JP3076682B2 (en) Alumina-based sintered body and method for producing the same
JPS61146762A (en) Antiabrasive silicon nitride base product
JP2808637B2 (en) Conductive zirconia sintered body
JPH069264A (en) Wc-al2o3 sintered composite compact
US4452906A (en) Ceramic composition
JP3051603B2 (en) Titanium compound sintered body
JPS6337069B2 (en)
JP2858965B2 (en) Aluminum oxide sintered body
JPH0122233B2 (en)
Kaiser et al. SI3N4/SIC composites using conventional and nanosized powders
JPS61270265A (en) High strength high tougness tib2 base composite sintered body
JPH0710747B2 (en) Boride-zirconium oxide-carbonitride ceramic materials
JP2001322009A (en) Alumina ceramic cutting tool and manufacturing method thereof
JPS6337068B2 (en)
JPS58130169A (en) Metal boride-zirconium oxide ceramic material
JPH02255561A (en) Al2o3-based composite sintered body and production thereof
JPS59232972A (en) Abrasion resistant sialon base ceramics
JPS63282166A (en) High-density metal boride-base sintered ceramics body
JPH0461828B2 (en)
JPH05124865A (en) Silicon nitride-based sintered compact