JPH0525937B2 - - Google Patents
Info
- Publication number
- JPH0525937B2 JPH0525937B2 JP24582583A JP24582583A JPH0525937B2 JP H0525937 B2 JPH0525937 B2 JP H0525937B2 JP 24582583 A JP24582583 A JP 24582583A JP 24582583 A JP24582583 A JP 24582583A JP H0525937 B2 JPH0525937 B2 JP H0525937B2
- Authority
- JP
- Japan
- Prior art keywords
- toughness
- sintered body
- pores
- cermet
- pore
- 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
- 239000011148 porous material Substances 0.000 claims description 54
- 239000011195 cermet Substances 0.000 claims description 20
- 239000002344 surface layer Substances 0.000 claims description 17
- 239000000758 substrate Substances 0.000 claims description 3
- 239000003795 chemical substances by application Substances 0.000 description 11
- 239000000203 mixture Substances 0.000 description 9
- NRTOMJZYCJJWKI-UHFFFAOYSA-N Titanium nitride Chemical compound [Ti]#N NRTOMJZYCJJWKI-UHFFFAOYSA-N 0.000 description 6
- 239000011268 mixed slurry Substances 0.000 description 6
- 238000010304 firing Methods 0.000 description 5
- 239000002002 slurry Substances 0.000 description 5
- 239000010936 titanium Substances 0.000 description 5
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 4
- 230000000694 effects Effects 0.000 description 4
- 239000000463 material Substances 0.000 description 3
- 239000002904 solvent Substances 0.000 description 3
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 2
- 239000010410 layer Substances 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 229910052719 titanium Inorganic materials 0.000 description 2
- 239000004698 Polyethylene Substances 0.000 description 1
- 229910000831 Steel Inorganic materials 0.000 description 1
- 238000013459 approach Methods 0.000 description 1
- 239000012298 atmosphere Substances 0.000 description 1
- 230000004888 barrier function Effects 0.000 description 1
- 239000000155 melt Substances 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 238000000465 moulding Methods 0.000 description 1
- 230000001590 oxidative effect Effects 0.000 description 1
- 239000012188 paraffin wax Substances 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- -1 polyethylene Polymers 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 230000002250 progressing effect Effects 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 239000010959 steel Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 239000001993 wax Substances 0.000 description 1
Landscapes
- Cutting Tools, Boring Holders, And Turrets (AREA)
- Powder Metallurgy (AREA)
Description
本発明は例えばスローアウエイインサート等の
切削工具用サーメツトに関するものである。
従来、この種サーメツトは一般に超硬合金と比
べ靱性が劣ることが知られ、この靱性を向上させ
るために、TiC基サーメツトに窒化チタン
(TiN)若しくは炭窒化チタン{Ti(C,N)}を
添加することにより靱性を向上させることが試み
られた。しかしながら、斯様な方法によつてはあ
る程度の靱性の向上は見られるものの超硬合金に
匹敵する程度まで靱性を向上させることが出来
ず、未だこの種サーメツトの高靱性化は充分に果
し得ていないのが現状である。因みに、従来の
TiC基サーメツトに窒化チタン(TiN)若しくは
炭窒化チタン{Ti(C,N)}を添加したものを
断続切削試験により、欠損までの平均衝撃回数に
よつてその靱性を測定すると、大凡800〜880回程
度であるのに対し、超硬合金の一例を示すとその
回数は2400回と遥かに優れている。
そこで、本発明はサーメツト基体の構造自体に
改良を加えることにより、該サーメツト基体の靱
性を上記の超硬合金に匹敵する程度又はそれ以上
にまで顕著に向上させ得ることを知見した。
本発明はサーメツト基体の表層が表面より厚み
0.01〜2.00mmに亘つて緻密質で、内部が焼結体表
面積の10〜50%のポアの占有面積を有するポア質
となるように焼成することにより、緻密な表層に
衝撃によりクラツクが生じた場合、そのクラツク
の内方への進展をポア質で阻止してクラツクが内
方又は全体に及ばないように抑制し、全体への破
損を防止する様にしたものである。
前記ポアの占有面積が10%以下の場合、即ちポ
アの数が少ないとクラツクの発生位置に対向する
ポアの数が少ないので、前記クラツクの進展を阻
止する効果が少なくまた逆に50%を越えると極端
に焼結体全体としての靱性が劣化する。緻密な表
層の厚みが2.00mmを越えると緻密質の占有面積が
増加し全体が緻密質である従来のものに近づき前
記クラツクの進展を阻止する効果が少なく、0.01
mm未満の場合ポア質の占有面積が大きくなり過ぎ
焼結体全体としての靱性が劣化する。
以下、本発明を三角形のスローアウエイインサ
ートに応用したサーメツト焼結体構造及びクラツ
ク発生状態を図面に基づき説明する。
第1図は該インサート基体の焼結状態の基本構
造を示す横断面図、第2図は同様のインサート基
体の縦断面図である。インサート基体1はTiC
{若しくはTiN,Ti(C,N)}基焼結体からな
り、表層を一定厚みTに亘つて緻密質2で形成
し、内部を一定占有面積を有するポア質3で図示
の如く形成する。
インサートの焼結体を斯様な構造とすることに
より、第3図に示す如く、インサート基体1表層
の緻密質2にクラツク(ひび割れ)C1が生じた
場合、このクラツクC1の進展はその先端がポア
質3内の1個のポアに至り、このポアによりクラ
ツクC1の先端がそれ以上進展をしない様に抑制
することができる。これに比較して、第4図に示
す全体が緻密質4である従来のサーメツトの場合
は、その靱性は焼結体の製法又は組成そのものに
依存し、ある程度の靱性を有するものでも、もし
その表層にクラツクC2が発生すると、その先端
は何んらクラツク進展を抑制する構造上の障壁が
ないから、容易に焼結体5の内部及び全体へ進展
して焼結体全体の破損を来たす。
上記のことから本発明の場合、焼結体1の緻密
な表層の厚みTが薄過ぎるとポア質の占める容積
が大きくなり過ぎ全体の靱性が劣化する。一方、
緻密な表層の厚みTが厚過ぎると緻密質の占める
容積が大きくなり過ぎクラツクの進展範囲が長く
なり従来例の靱性の少ない特性に近ずく。また、
ポア質のポア占有面積が小さ過ぎるとクラツクの
発生位置に対応してポアが占める数が減少し、ク
ラツクの進展範囲が大きくなるかまたは内部への
進展を許すことになる。一方、ポア質のポア占有
面積が大き過ぎると全体の靱性が劣化する。さら
に、ポアの平均径は0.5μm〜5μmの範囲が適当で
あり、それより大き過ぎると全体の靱性が劣化
し、小さ過ぎるとクラツク進展に対する抑制効果
が小さくなる。
次に上記の焼結体を得る適当な製法の例を説明
する。
実施例 1
出発原料としてTiC,TiN,WC,Mo2C及び
Niを第1表に示す組成範囲となるように秤量し、
これにアセトン等の適当な溶剤を加え、振動ミル
により湿式混合を行ない混合スラリーを作成す
る。この混合スラリーにポリエチレン等のポア剤
を適量加えてサイド混合を行う。混合終了後乾燥
し溶剤を蒸発除去すると共にパラフインワツクス
を添加して40メツシユパスして製粒する。かくし
て得られた粉末を1000〜2000Kg/cm2の圧力で成形
し、その後300℃前後の温度で仮焼してワツクス
を除去した後、更に非酸化性雰囲気中で1500℃の
焼成温度にて焼成する。前記ポア剤は500〜1000
℃で溶け、成型体のポア剤の占めていた部分がポ
アとして残る。この際、焼結体は若干収縮するた
め、前記スラリ中には得ようとするポア径(後述
する)より少し大きめ(約1.2倍)の粒径を有す
るポア剤を用いる。
さらに、前記ポア剤を添加しない上記と同様の
混合スラリーを前記焼成体の全面に塗布する。塗
布するスラリーの厚みは焼成時の収縮率に応じて
適当な厚みとする。その後、塗布したスラリーが
充分乾燥した後1500℃の焼成温度で焼成して内部
にポア質を、表層に緻密質を有する焼結体とす
る。
斯様にして前記TiC,TiNの組成範囲を40:20
重量%又は20:40重量%を含む2組のサーメツト
組成について、前記ポア質の焼成体に塗布するス
ラリーの量を調整して緻密な表層の厚みを決定
し、また前記ポア剤の添加量を調整して焼結体内
のポアの占有面積を決定して、内接円直径9.5mm、
厚み4.8mmの各三角形状インサートとして第1表
に示す1〜8の試料とし、これら各試料について
断続切削試験による焼結体の欠損までの平均衝撃
回数を求めた。
The present invention relates to a cermet for cutting tools such as throw-away inserts. Conventionally, it is known that this type of cermet is generally inferior in toughness compared to cemented carbide, and in order to improve this toughness, titanium nitride (TiN) or titanium carbonitride {Ti(C,N)} has been added to TiC-based cermet. Attempts have been made to improve toughness by adding C. However, although such a method improves the toughness to a certain extent, it has not been possible to improve the toughness to a level comparable to that of cemented carbide, and it has not yet been possible to sufficiently improve the toughness of this type of cermet. The current situation is that this is not the case. By the way, the conventional
When titanium nitride (TiN) or titanium carbonitride {Ti(C,N)} is added to a TiC-based cermet, its toughness is measured by the average number of impacts until fracture in an intermittent cutting test, and the toughness is approximately 800 to 880. In contrast, an example of cemented carbide has a far superior number of times of 2,400 times. Accordingly, the present invention has found that by improving the structure of the cermet substrate itself, the toughness of the cermet substrate can be significantly improved to a level comparable to or even higher than that of the above-mentioned cemented carbide. In the present invention, the surface layer of the cermet base is thicker than the surface.
By firing the material so that it is dense with a diameter of 0.01 to 2.00 mm and has pores occupying an area of 10 to 50% of the surface area of the sintered body, cracks occur in the dense surface layer due to impact. In this case, the inward propagation of the crack is blocked by the porous material to prevent the crack from extending inward or to the whole body, thereby preventing damage to the whole body. When the occupied area of the pores is less than 10%, that is, when the number of pores is small, the number of pores facing the crack occurrence position is small, so the effect of preventing the crack from progressing is small, and conversely, when the area occupied by the pores is less than 50% The toughness of the sintered body as a whole deteriorates extremely. When the thickness of the dense surface layer exceeds 2.00 mm, the area occupied by the dense layer increases and approaches the conventional case where the entire surface layer is dense, and the effect of preventing the development of cracks is small, and the thickness is less than 0.01 mm.
If it is less than mm, the area occupied by the pores becomes too large and the toughness of the sintered body as a whole deteriorates. Hereinafter, the structure of a cermet sintered body in which the present invention is applied to a triangular throw-away insert and the state of occurrence of cracks will be explained based on the drawings. FIG. 1 is a cross-sectional view showing the basic structure of the insert base in a sintered state, and FIG. 2 is a longitudinal cross-sectional view of the same insert base. Insert base 1 is TiC
It is made of {or TiN, Ti(C,N)} based sintered body, the surface layer is formed of a dense material 2 over a certain thickness T, and the inside is formed of a porous material 3 having a certain occupied area as shown in the figure. By making the sintered body of the insert into such a structure, as shown in FIG . The tip reaches one pore in the porous substance 3, and this pore can prevent the tip of the crack C1 from advancing any further. In comparison, in the case of the conventional cermet shown in Fig. 4, which is entirely dense 4, its toughness depends on the manufacturing method or composition itself of the sintered body, and even if it has a certain degree of toughness, if When a crack C 2 occurs on the surface layer, since there is no structural barrier at the tip to suppress crack propagation, it easily propagates into the entire sintered body 5 and causes damage to the entire sintered body. . From the above, in the case of the present invention, if the thickness T of the dense surface layer of the sintered body 1 is too thin, the volume occupied by the pores becomes too large and the overall toughness deteriorates. on the other hand,
If the thickness T of the dense surface layer is too large, the volume occupied by the dense layer becomes too large, and the range of crack development becomes long, approaching the low toughness characteristics of the conventional example. Also,
If the area occupied by the pores of the porous material is too small, the number of pores occupied by the crack will decrease in proportion to the location where the crack occurs, and the range of crack development will become larger or the crack will be allowed to grow inward. On the other hand, if the area occupied by the pores of the porous material is too large, the overall toughness will deteriorate. Furthermore, the average diameter of the pores is suitably in the range of 0.5 μm to 5 μm; if it is too large, the overall toughness will deteriorate, and if it is too small, the effect of suppressing crack growth will be reduced. Next, an example of a suitable manufacturing method for obtaining the above sintered body will be explained. Example 1 TiC, TiN, WC, Mo 2 C and
Weigh Ni so that it has the composition range shown in Table 1,
A suitable solvent such as acetone is added to this, and wet mixing is performed using a vibrating mill to create a mixed slurry. An appropriate amount of a pore agent such as polyethylene is added to this mixed slurry and side mixing is performed. After the mixing is completed, the mixture is dried, the solvent is evaporated off, paraffin wax is added, and the mixture is granulated by 40 mesh passes. The powder thus obtained is molded at a pressure of 1000 to 2000 Kg/ cm2 , then calcined at a temperature of around 300°C to remove wax, and then fired at a firing temperature of 1500°C in a non-oxidizing atmosphere. do. The pore agent is 500~1000
It melts at ℃, leaving the part of the molded body occupied by the pore agent as pores. At this time, since the sintered body shrinks slightly, a pore agent having a particle size slightly larger (approximately 1.2 times) than the desired pore diameter (described later) is used in the slurry. Furthermore, a mixed slurry similar to the above without adding the pore agent is applied to the entire surface of the fired body. The thickness of the slurry to be applied is determined appropriately depending on the shrinkage rate during firing. Thereafter, after the applied slurry is sufficiently dried, it is fired at a firing temperature of 1500°C to form a sintered body having a porous interior and a dense surface layer. In this way, the composition range of TiC and TiN was adjusted to 40:20.
For two sets of cermet compositions containing 20:40% by weight or 20:40% by weight, the thickness of the dense surface layer was determined by adjusting the amount of slurry applied to the porous fired body, and the amount of the pore agent added was determined. Adjust the area occupied by the pore in the sintered body, and the inscribed circle diameter is 9.5 mm.
Samples 1 to 8 shown in Table 1 were used as triangular inserts having a thickness of 4.8 mm, and the average number of impacts until the sintered body broke was determined by an interrupted cutting test for each sample.
【表】【table】
【表】
第1表の試料番号1及び5はポア剤無添加でポ
ア占有面積が0%であり、従来のサーメツトに相
当するものである。該試料番号1及び5は欠損ま
での平均衝撃回数が800及び880程度であるのに対
し、試料番号2,3,4,6,7及び8は焼結体
内部のポア質のポアの占有面積が10〜50%で、そ
の欠損までの平均衝撃回数は1380以上とポアの占
有面積が0%の従来サーメツトより!?かに靱性が
向上していることが分り、特に試料番号3、及び
7のものは前記衝撃回数が2340及び2400と前述し
た超硬合金の靱性に匹敵する程度まで向上してい
ることが理解できる。
また、上記試料番号3及び4と同じポア占有面
積が30%である試料番号3a,3b,7a、及び7bの
場合でも表層の緻密質の厚みが0.01mm未満又は
2.00mmを超えるとその衝撃回数が900以下となり
靱性が劣化することが理解される。
実施例 2
出発原料としてNbC,TiC,WC,TiN,Mo2
C及びNiを第2表に示す組成範囲となるように
秤量し、これにアセトン等の適当な溶剤を加え、
振動ミルにより湿式混合を行い混合スラリーを作
成する。この混合スラリーに前記と同様ポア剤を
適量加えて成型・焼成し、ポア質を有する成型さ
れた焼成体を得る。この焼成体に前記と同様ポア
剤を添加しない同様の混合スラリーを全面に塗布
し、これを焼成することにより、内部にポア質
を、表層に緻密質を有する焼結体を得る。
斯様にして上記の組成を適当なサーメツトの組
成範囲とし、前記ポア質の焼成体に塗布するスラ
リーの量を調整して緻密な表層の厚みを決定し、
また前記ポア剤の添加量を調整して焼結体内のポ
アの占有面積を決定し、前記と同様内接円直径
9.5mm、厚み4.8mmの各三角形状インサートとして
第2表に示す9〜16の試料とし、これら各試料に
ついて同様の断続切削試験による焼結体の欠損ま
での平均衝撃回数を求めた。[Table] Sample numbers 1 and 5 in Table 1 have no pore agent added and the pore occupied area is 0%, and correspond to conventional cermets. Sample numbers 1 and 5 have an average number of impacts before breakage of about 800 and 880, while sample numbers 2, 3, 4, 6, 7, and 8 have an area occupied by porous pores inside the sintered body. cermet is 10 to 50%, and the average number of impacts before breakage is over 1380, which shows that the toughness is significantly improved compared to the conventional cermet with 0% pore occupation area, especially sample numbers 3 and 7. It can be seen that the toughness of the steels with the same number of impacts has been improved to 2340 and 2400, comparable to the toughness of the cemented carbide mentioned above. In addition, even in the case of sample numbers 3a, 3b, 7a, and 7b, which have the same pore occupation area of 30% as sample numbers 3 and 4 above, the thickness of the dense surface layer is less than 0.01 mm or
It is understood that if it exceeds 2.00 mm, the number of impacts will be less than 900 and the toughness will deteriorate. Example 2 NbC, TiC, WC, TiN, Mo 2 as starting materials
Weigh C and Ni so that they fall within the composition range shown in Table 2, add a suitable solvent such as acetone,
Wet mixing is performed using a vibrating mill to create a mixed slurry. A suitable amount of a pore agent is added to this mixed slurry in the same manner as described above, followed by molding and firing to obtain a molded fired body having pores. A similar mixed slurry without the addition of a pore agent as described above is applied to the entire surface of this sintered body, and this is fired to obtain a sintered body having pores inside and a dense surface layer. In this way, the above composition is set as an appropriate composition range of the cermet, and the amount of slurry applied to the porous fired body is adjusted to determine the thickness of the dense surface layer.
In addition, the area occupied by the pores in the sintered body was determined by adjusting the amount of the pore agent added, and the inscribed circle diameter was determined in the same manner as above.
Samples 9 to 16 shown in Table 2 were prepared as triangular inserts each having a diameter of 9.5 mm and a thickness of 4.8 mm, and the average number of impacts until the sintered body fractured was determined using the same interrupted cutting test for each of these samples.
【表】【table】
【表】
第2表の試料番号9及び13はポア剤無添加でポ
ア占有面積が0%であり、従来のサーメツトに相
当するものである。試料番号9及び13は欠損まで
の平均衝撃回数が930及び900程度の靱性であるの
に対し、試料番号10,11,12,14,15及び16は焼
結体内部のポア質のポアの占有面積が10〜50%
で、その欠損までの平均衝撃回数は1380以上とポ
アの占有面積が0%の従来サーメツトより遥かに
靱性が優れていることが分り、特に試料番号11及
び15のものは前記衝撃回数が2430及び2620と実施
例1の試料番号3、及び7のものより優れている
のみならず前述の超硬合金のそれ以上の靱性が得
られていることが理解される。
また、上記試料番号11及び15と同じポア占有面
積が30%である試料番号11a,11b,15a及び15b
の場合でも表層の緻密質の厚みが0.01mm未満又は
2.00%mmを超えると、その衝撃回数が900以下と
なり実施例1と同様に靱性が劣化することが理解
される。
実施例 3
上記実施例1,2の試例番号3,7,11及び15
のものについて焼結体内部のポア質のポア平均径
が0.5μm未満と5μmを超える場合とについて同様
に断続切削試険による焼結体の欠損までの平均衝
撃回数を求めたところ、ポアの平均径が0.5μm未
満の場合は800〜900回、5μmを超えると500回程
度と靱性が極度に劣化した。即ち、ポアの平均径
が小さ過ぎるとクラツクの先端はポアの存在に関
係なく進展してしまいクラツク進展の抑制効果が
なくなり、逆にポアの平均径が大き過ぎると焼結
体全体の靱性が劣化するためである。
上記実施例1,2及び3からTiC基サーメツト
及び他のNbCを含むサーメツトにおいても、そ
の基体の表層が表面から厚み0.01〜2.00mmに亘つ
て緻密質で、内部が焼結体表面積の10〜50%のポ
アの占有面積を有するポア質となる様にした焼結
体は、内部に上記のポア質を形成しない従来のサ
ーメツトに比べその靱性が遥かに優れ、かつ超硬
合金の靱性と略同等若しくはそれ以上に向上する
ことが分かつた。また、ポア質のポア平均径が
0.5μm〜5μmの範囲外であると極度に靱性が劣化
することも理解される。そして、この様な焼結体
をスローアウイインサート等の切削工具用サーメ
ツトとして使用した場合、高靱性な耐久性に優れ
た切削工具を提供することができるものである。[Table] Sample numbers 9 and 13 in Table 2 have no pore agent added and the pore occupied area is 0%, and correspond to conventional cermets. Sample numbers 9 and 13 have toughness with an average number of impacts before fracture of about 930 and 900, while sample numbers 10, 11, 12, 14, 15 and 16 have toughness due to the occupation of porous pores inside the sintered body. Area is 10-50%
The average number of impacts before breakage was 1380 or more, which shows that the toughness is far superior to that of conventional cermets with 0% pore occupation area.In particular, sample numbers 11 and 15 have an average number of impacts of 2430 and above. It is understood that toughness is not only superior to that of 2620 and Sample Nos. 3 and 7 of Example 1, but also greater than that of the cemented carbide described above. In addition, sample numbers 11a, 11b, 15a and 15b have the same pore occupation area of 30% as sample numbers 11 and 15 above.
Even if the thickness of the surface layer is less than 0.01mm or
It is understood that if it exceeds 2.00% mm, the number of impacts will be 900 or less, and the toughness will deteriorate as in Example 1. Example 3 Sample numbers 3, 7, 11 and 15 of Examples 1 and 2 above
When the average number of impacts until the sintered body breaks due to an interrupted cutting test was similarly calculated for cases where the average diameter of the pores inside the sintered body was less than 0.5 μm and more than 5 μm, the average number of impacts until the sintered body fractured was determined. When the diameter was less than 0.5 μm, it was repeated 800 to 900 times, and when it exceeded 5 μm, the toughness was extremely deteriorated. In other words, if the average diameter of the pores is too small, the tip of the crack will develop regardless of the presence of pores, and the effect of suppressing crack growth will be lost.On the other hand, if the average diameter of the pores is too large, the toughness of the entire sintered body will deteriorate. This is to do so. From the above Examples 1, 2, and 3, the TiC-based cermet and other NbC-containing cermets also have a dense surface layer from the surface to a thickness of 0.01 to 2.00 mm, and an inner surface area of 10 to 2.00 mm of the surface area of the sintered body. The sintered body, which has a porous structure with an area occupied by 50% pores, has far superior toughness compared to conventional cermets that do not have the above-mentioned pores inside, and has a toughness comparable to that of cemented carbide. It was found that the improvement was the same or even better. In addition, the average pore diameter of the pore quality is
It is also understood that outside the range of 0.5 μm to 5 μm, the toughness is extremely degraded. When such a sintered body is used as a cermet for a cutting tool such as a throw-eye insert, a cutting tool with high toughness and excellent durability can be provided.
第1図乃至第3図は本発明を三角形のスローア
ウエイインサートに応用したサーメツト焼結体構
造及びクラツク発生状態を示すもので、第1図は
インサートの横断面図、第2図は同様のインサー
トの縦断面図、第3図はクラツク発生状態を示す
拡大部分説明図であり、第4図は焼結体全体が緻
密質である従来のインサートのクラツク発生状態
を示す拡大部分説明図である。
1……インサート基体、2……緻密質、3……
ポア質、T……表層厚み。
Figures 1 to 3 show the structure of a cermet sintered body and the state of crack occurrence in which the present invention is applied to a triangular throw-away insert. Figure 1 is a cross-sectional view of the insert, and Figure 2 is a similar insert. FIG. 3 is an enlarged partial explanatory view showing a crack occurrence state, and FIG. 4 is an enlarged partial explanatory view showing a crack occurrence state of a conventional insert in which the entire sintered body is dense. 1...Insert base, 2...Dense material, 3...
Pore quality, T...surface layer thickness.
Claims (1)
2.00mmに亘つて緻密質で、内部が焼結体表面積の
10〜50%のボアの占有面積を有するポア質となる
ように焼成したことを特徴とする高靱性サーメツ
ト。 2 前記ポア質のポア平均径が0.5μm〜5μmであ
ることを特徴とする特許請求の範囲第1項記載の
高靱性サーメツト。[Claims] 1. The surface layer of the cermet substrate is 0.01 to 0.01 thicker than the surface.
It is dense over 2.00mm, and the inside has a sintered body surface area.
A high-toughness cermet characterized by being fired to form a porous material having an area occupied by 10 to 50% of the bore. 2. The high toughness cermet according to claim 1, wherein the pores have an average pore diameter of 0.5 μm to 5 μm.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP24582583A JPS60138042A (en) | 1983-12-27 | 1983-12-27 | High toughness cermet |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP24582583A JPS60138042A (en) | 1983-12-27 | 1983-12-27 | High toughness cermet |
Related Child Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2174062A Division JPH0663052B2 (en) | 1990-06-29 | 1990-06-29 | High toughness cermet tool |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS60138042A JPS60138042A (en) | 1985-07-22 |
| JPH0525937B2 true JPH0525937B2 (en) | 1993-04-14 |
Family
ID=17139411
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP24582583A Granted JPS60138042A (en) | 1983-12-27 | 1983-12-27 | High toughness cermet |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS60138042A (en) |
Families Citing this family (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| SE510284C2 (en) * | 1996-11-18 | 1999-05-10 | Sandvik Ab | Internally chilled cutter for chip separating machining |
| JP5276392B2 (en) * | 2007-09-21 | 2013-08-28 | 住友電気工業株式会社 | Cutting tool and method of manufacturing cutting tool |
| US9127335B2 (en) | 2009-04-27 | 2015-09-08 | Sandvik Intellectual Property Ab | Cemented carbide tools |
-
1983
- 1983-12-27 JP JP24582583A patent/JPS60138042A/en active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| JPS60138042A (en) | 1985-07-22 |
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