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JPH0240030B2 - SERAMITSUKUZAITOSAAMETSUTOZAITONOSETSUGOHOHO - Google Patents
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JPH0240030B2 - SERAMITSUKUZAITOSAAMETSUTOZAITONOSETSUGOHOHO - Google Patents

SERAMITSUKUZAITOSAAMETSUTOZAITONOSETSUGOHOHO

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Publication number
JPH0240030B2
JPH0240030B2 JP17066985A JP17066985A JPH0240030B2 JP H0240030 B2 JPH0240030 B2 JP H0240030B2 JP 17066985 A JP17066985 A JP 17066985A JP 17066985 A JP17066985 A JP 17066985A JP H0240030 B2 JPH0240030 B2 JP H0240030B2
Authority
JP
Japan
Prior art keywords
tic
cermet
weight
chromium carbide
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 - Lifetime
Application number
JP17066985A
Other languages
Japanese (ja)
Other versions
JPS6230674A (en
Inventor
Mitsuhiko Furukawa
Osamu Nakano
Tetsunori Kitada
Hisashi Hiraishi
Yoshiaki Yamagami
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.)
Kubota Corp
Original Assignee
Kubota 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 Kubota Corp filed Critical Kubota Corp
Priority to JP17066985A priority Critical patent/JPH0240030B2/en
Publication of JPS6230674A publication Critical patent/JPS6230674A/en
Publication of JPH0240030B2 publication Critical patent/JPH0240030B2/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

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  • Pressure Welding/Diffusion-Bonding (AREA)
  • Ceramic Products (AREA)

Description

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

<産業上の利用分野> 本発明は、耐熱、耐摩性等に優れた炭化クロム
セラミツクを各種用途に用いるに際し、その靭性
不足を補う為にサーメツトと組合わせて使用する
場合の両者の接合方法に関するものである。 <従来の技術> 従来からのセラミツク材とサーメツト材の接合
は主として次の如き方法である。即ち、 (a) 焼嵌め、圧入等により機械的に接合する方法 (b) ロー剤等接着剤を用いる方法 (c) 両者間に荷重又はガス圧をかけた状態で高温
加熱する方法 であつた。 <発明が解決しようとする問題点> 上記従来方法である(a)は、セラミツクとサーメ
ツトとの熱膨張率の差がある為に、使用可能な温
度領域が狭い範囲に限られるという問題があり、
又(b)の方法は適当な熱膨張率を有する接着剤の選
定の困難さ、及び高温域では使用不可能という問
題があり、更に(c)の方法では、加熱処理中に大き
な機械的荷重あるいは高いガス圧をかけなければ
ならない為に、作業が煩雑あるいは大規模な装置
を必要とする等の問題があつた。 <問題点を解決する為の手段> 本発明では上述の諸問題を解決し、簡単な方法
によりセラミツク材とサーメツト材とを強固に接
合する為に両者の組成をある範囲に限定したもの
であつて、その要旨は炭化クロムから成るセラミ
ツク材と、TiC0.5〜48重量%、Ni5〜40重量℃、
残部が炭化クロムより成り、しかもTiCとNiの
重量比TiC/Ni≦1.2である様なサーメツト材と
を当接状態下、即ち、面合わせ後何ら荷重をかけ
ることなく加熱することを特徴とするセラミツク
材とサーメツト材との接合方法である。 なお、上記本発明方法に於いて、加熱時の雰囲
気は、酸化を防止する為に10-2torr.以下の真空
中、水素ガス中あるいはアルゴンガス中等の非酸
化性雰囲気とする様にし、加熱は通常1250〜1350
℃の温度で60分間位行なうものとする。又セラミ
ツク材とサーメツト材との両接合面はRmax.3.0μ
m以下程度に仕上げておくものとする。 本発明方法での炭化ロム材は、Cr3C2、Cr7C3
Cr23C6等であり、それらのいずれか1種又は二種
以上の組合わせでもよい。又サーメツト材の一成
分としての炭化クロムも同様である。 <実施例及び作用> 以下本発明方法についての実施例並びに比較例
につきその諸性質を挙げ乍ら本発明方法を詳述す
る。 セラミツク材としては、純度99.9%以上、平均
粒径5μmの炭化クロム粉末100重量部に対し、パ
ラフイン3重量部を添加混合した原料を、成形圧
1.5トン/cm2で、20×20×5(mm)に成形し、780
℃、10分間真空中にて予備焼結をし、次いで真空
中で1450℃、60分間本焼結を行つて得た焼結体を
用いた。 又サーメツト材としては、純度99.9%以上、平
均粒径5μmの炭化クロム(Cr3C2)粒末と、同じ
く純度99.9%以上、平均粒径5μmの炭化チタン
(TiC)粉末及びNi粉末とを下表に示す割合で混
合した粉末100重量部に対し、パラフイン3重量
部を添加し、均一に混練した後、成形圧1.5ト
ン/cm2で、20×20×5(mm)に成形し、780℃、10
分間真空中にて予備焼結をし、次いで真空中で
1350℃、60分間本焼結を行つて得た焼結体を用い
た。 上述の如くして得たセラミツク材とサーメツト
材とのそれぞれの接合面をRmax.3.0μm以下とな
る様に面仕上げをなし、両者を無負荷の接合状態
で10-2torr.以下の真空中1250〜1350℃で60分間加
熱処理を行つた。 この様にして接合されたセラミツク材とサーメ
ツト材との接合強度と接合後のクラツクの有無を
下表に示す。クラツクの有無とは、接合後にセラ
ミツク材側に入る割れを観察したもので〇は割れ
なし、×は割れが入つた事を示す。 なお下表中にはサーメツト材の熱膨張係数αを
も併記した。下表についてはNi、TiC,Cr3C2
ついての単位は重量%、接合強度の単位はKg/
mm2、又αは1000℃に於ける熱膨張係数を示しその
単位は、℃-1×10-6である。
<Field of Industrial Application> The present invention relates to a method for joining chromium carbide ceramic, which has excellent heat resistance, wear resistance, etc., when used in combination with cermet to compensate for its lack of toughness when used for various purposes. It is something. <Prior Art> Conventional methods for joining ceramic materials and cermet materials are mainly as follows. That is, (a) a method of mechanically joining by shrink fitting, press-fitting, etc., (b) a method of using an adhesive such as a brazing agent, and (c) a method of heating at high temperature while applying a load or gas pressure between the two. . <Problems to be Solved by the Invention> The above conventional method (a) has the problem that the usable temperature range is limited to a narrow range due to the difference in thermal expansion coefficient between ceramic and cermet. ,
In addition, method (b) has problems in that it is difficult to select an adhesive with an appropriate coefficient of thermal expansion and cannot be used in a high temperature range.Furthermore, method (c) requires a large mechanical load during heat treatment. Alternatively, since high gas pressure must be applied, there are problems such as complicated work or the need for large-scale equipment. <Means for Solving the Problems> The present invention solves the above-mentioned problems and limits the composition of the ceramic material and cermet material to a certain range in order to firmly bond them together by a simple method. The gist of this is that a ceramic material consisting of chromium carbide, TiC 0.5 to 48% by weight, Ni 5 to 40% by weight,
It is characterized by heating a cermet material of which the remainder is chromium carbide and the weight ratio of TiC and Ni is TiC/Ni≦1.2 under abutting conditions, that is, without applying any load after face-to-face contact. This is a method of joining ceramic materials and cermet materials. In the above method of the present invention, the atmosphere during heating is a non-oxidizing atmosphere such as a vacuum of 10 -2 torr or less, hydrogen gas, or argon gas to prevent oxidation. is usually 1250-1350
The test shall be carried out for approximately 60 minutes at a temperature of ℃. Also, both bonding surfaces of ceramic material and cermet material have Rmax.3.0μ.
It shall be finished to a length of no more than m. The chromium carbide material used in the method of the present invention includes Cr 3 C 2 , Cr 7 C 3 ,
Cr 23 C 6, etc., and any one of them or a combination of two or more thereof may be used. The same applies to chromium carbide as a component of cermet materials. <Examples and Effects> The method of the present invention will be described in detail below while citing various properties of Examples and Comparative Examples of the method of the present invention. As a ceramic material, a raw material is prepared by adding 3 parts by weight of paraffin to 100 parts by weight of chromium carbide powder with a purity of 99.9% or more and an average particle size of 5 μm.
1.5 tons/ cm2 , molded to 20 x 20 x 5 (mm), 780
A sintered body obtained by preliminary sintering in a vacuum at 1450°C for 10 minutes and then main sintering in a vacuum at 1450°C for 60 minutes was used. The cermet materials used include chromium carbide (Cr 3 C 2 ) powder with a purity of 99.9% or higher and an average particle size of 5 μm, and titanium carbide (TiC) powder and Ni powder with a purity of 99.9% or higher and an average particle size of 5 μm. 3 parts by weight of paraffin was added to 100 parts by weight of the powder mixed in the proportions shown in the table below, and after kneading it uniformly, it was molded into a size of 20 x 20 x 5 (mm) at a molding pressure of 1.5 tons/ cm2 . 780℃, 10
Pre-sintering in vacuum for minutes, then in vacuum
A sintered body obtained by performing main sintering at 1350°C for 60 minutes was used. The bonded surfaces of the ceramic material and cermet material obtained as described above were finished so that the Rmax.3.0 μm or less was achieved, and both were bonded together under no load in a vacuum of 10 -2 torr. or less. Heat treatment was performed at 1250-1350°C for 60 minutes. The table below shows the bonding strength of the ceramic material and cermet material bonded in this manner and the presence or absence of cracks after bonding. The presence or absence of cracks refers to the observation of cracks entering the ceramic material side after joining. ○ indicates no cracks, and × indicates cracks. In addition, the thermal expansion coefficient α of the cermet material is also listed in the table below. In the table below, the unit for Ni, TiC, Cr3C2 is weight%, and the unit for joint strength is Kg/
mm 2 and α represent the coefficient of thermal expansion at 1000°C, and its unit is °C -1 ×10 -6 .

【表】【table】

【表】【table】

【表】【table】

【表】【table】

【表】【table】

【表】 上述の表に示す結果から次の事が判明する。即
ちサーメツト材の組成によりセラミツク材との接
合強度に大きな変化があり、炭化クロム100%か
ら成るセラミツク材に対しては次の様な組成のサ
ーメツトが望ましい。まずTiCの量については、
Ni量が同じであればTiCが0の場合と、TiCが10
重量%未満の場合でその接合強度は殆んど変わら
ない、しかしサーメツト材の抗折強度を維持する
為にはTiCは最少でも0.5重量%は添加する必要
がある。一方TiCそれ自体ではCr3C2との接合性
は良くはなくTiCを増せばバインダー的役割の
Niをも増加する必要があり、その様にTiCとNi
とをあまり増せばサーメツト中のCr3C2の量が少
なくなり相手材たるCr3C2との整合性が悪くなる
と共に、Ni増加に起因して液相の発生が増え、
界面に於けるCr3C2の粒成長を促進させるという
問題がある。 この様な理由からTiCの上限は48重量%(試料
No.71参照)とし、Niは十分な接合強度を発現す
るに要な液相を生ずる為に最少5重量%とし、逆
に40重量%を越えると液相の発生が多くなりすぎ
てCr3C2の粒成長に伴ないクラツクが発生し易く
なる(試料No.73〜76、78参照)と共に、熱膨張係
数αが相手材たるCr3C2の11.6×10-6-1から大
きく離れすぎるので40重量%以下とする。更に上
述した如くTiCの量とNiの量との間にはある一
定の関係を持たせるべきであり、上表で接合強度
が10Kg/mm2以上となる組合わせとしてTiC/Ni
≦1.2とした。 <発明の効果> 以上述べて来た如く、本発明方法によればセラ
ミツク材とサーメツト材とが、それらを無負荷で
単に当接させた状態で加熱するという簡単な操作
により、十分の接合強度を持つて接合される。従
つて炭化クロムが有する耐熱性、耐食性等にセラ
ミツクとしての利点を活かしつゝ、靭性に乏しい
という欠点にサーメツト材で補強し各種の幅広い
用途に用いる事が出来るものである。
[Table] From the results shown in the table above, the following is clear. That is, the bonding strength with the ceramic material varies greatly depending on the composition of the cermet material, and it is desirable to use a cermet with the following composition for a ceramic material made of 100% chromium carbide. First of all, regarding the amount of TiC,
If the amount of Ni is the same, TiC is 0 and TiC is 10.
If the TiC content is less than 0.5% by weight, the bonding strength will hardly change, but in order to maintain the bending strength of the cermet material, it is necessary to add at least 0.5% by weight of TiC. On the other hand, TiC itself does not have good bonding properties with Cr 3 C 2 , and increasing TiC reduces its role as a binder.
It is also necessary to increase Ni, and in the same way TiC and Ni
If the amount of Cr 3 C 2 is increased too much, the amount of Cr 3 C 2 in the cermet will decrease and the compatibility with the mating material Cr 3 C 2 will deteriorate, and the generation of liquid phase will increase due to the increase in Ni.
There is a problem of promoting grain growth of Cr 3 C 2 at the interface. For these reasons, the upper limit of TiC is 48% by weight (sample
(Refer to No. 71), and the Ni content should be at least 5% by weight in order to generate the liquid phase necessary to develop sufficient bonding strength.On the other hand, if it exceeds 40% by weight, too much liquid phase will occur and Cr 3 Cracks are more likely to occur due to the grain growth of C 2 (see sample Nos. 73 to 76, 78), and the thermal expansion coefficient α is larger than the 11.6×10 -6-1 of the mating material Cr 3 C 2. Since they are too far apart, it should be 40% by weight or less. Furthermore, as mentioned above, there should be a certain relationship between the amount of TiC and the amount of Ni.
≦1.2. <Effects of the Invention> As described above, according to the method of the present invention, sufficient bonding strength can be achieved by simply heating a ceramic material and a cermet material in a state in which they are brought into contact with each other without any load. It is joined by holding it. Therefore, while taking advantage of the heat resistance and corrosion resistance of chromium carbide as a ceramic, it can be used in a wide variety of applications by reinforcing the drawback of poor toughness with a cermet material.

Claims (1)

【特許請求の範囲】[Claims] 1 炭化クロムから成るセラミツク材と、
TiC0.5〜48重量%、Ni5〜40重量%、残部が炭化
クロムより成り、しかもTiCとNiの重量比TiC/
Ni≦1.2である様なサーメツト材とを当接状態下
で加熱することを特徴とするセラミツク材とサー
メツト材との接合方法。
1 Ceramic material made of chromium carbide,
It consists of 0.5 to 48% by weight of TiC, 5 to 40% by weight of Ni, and the balance is chromium carbide, and the weight ratio of TiC to Ni is TiC/
A method for joining a ceramic material and a cermet material, which is characterized by heating the cermet material such that Ni≦1.2 in contact with the material.
JP17066985A 1985-08-01 1985-08-01 SERAMITSUKUZAITOSAAMETSUTOZAITONOSETSUGOHOHO Expired - Lifetime JPH0240030B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP17066985A JPH0240030B2 (en) 1985-08-01 1985-08-01 SERAMITSUKUZAITOSAAMETSUTOZAITONOSETSUGOHOHO

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP17066985A JPH0240030B2 (en) 1985-08-01 1985-08-01 SERAMITSUKUZAITOSAAMETSUTOZAITONOSETSUGOHOHO

Publications (2)

Publication Number Publication Date
JPS6230674A JPS6230674A (en) 1987-02-09
JPH0240030B2 true JPH0240030B2 (en) 1990-09-10

Family

ID=15909179

Family Applications (1)

Application Number Title Priority Date Filing Date
JP17066985A Expired - Lifetime JPH0240030B2 (en) 1985-08-01 1985-08-01 SERAMITSUKUZAITOSAAMETSUTOZAITONOSETSUGOHOHO

Country Status (1)

Country Link
JP (1) JPH0240030B2 (en)

Also Published As

Publication number Publication date
JPS6230674A (en) 1987-02-09

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