JPH0526599B2 - - Google Patents

Info

Publication number
JPH0526599B2
JPH0526599B2 JP1146086A JP1146086A JPH0526599B2 JP H0526599 B2 JPH0526599 B2 JP H0526599B2 JP 1146086 A JP1146086 A JP 1146086A JP 1146086 A JP1146086 A JP 1146086A JP H0526599 B2 JPH0526599 B2 JP H0526599B2
Authority
JP
Japan
Prior art keywords
solder
metal
intermediate material
active metal
alloy
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
JP1146086A
Other languages
Japanese (ja)
Other versions
JPS62168694A (en
Inventor
Kozo Kashiwagi
Hidekazu Yanagisawa
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.)
Tanaka Kikinzoku Kogyo KK
Original Assignee
Tanaka Kikinzoku Kogyo KK
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 Tanaka Kikinzoku Kogyo KK filed Critical Tanaka Kikinzoku Kogyo KK
Priority to JP1146086A priority Critical patent/JPS62168694A/en
Publication of JPS62168694A publication Critical patent/JPS62168694A/en
Publication of JPH0526599B2 publication Critical patent/JPH0526599B2/ja
Granted legal-status Critical Current

Links

Classifications

    • BPERFORMING OPERATIONS; TRANSPORTING
    • B23MACHINE TOOLS; METAL-WORKING NOT OTHERWISE PROVIDED FOR
    • B23KSOLDERING OR UNSOLDERING; WELDING; CLADDING OR PLATING BY SOLDERING OR WELDING; CUTTING BY APPLYING HEAT LOCALLY, e.g. FLAME CUTTING; WORKING BY LASER BEAM
    • B23K35/00Rods, electrodes, materials, or media, for use in soldering, welding, or cutting
    • B23K35/22Rods, electrodes, materials, or media, for use in soldering, welding, or cutting characterised by the composition or nature of the material
    • B23K35/24Selection of soldering or welding materials proper
    • B23K35/30Selection of soldering or welding materials proper with the principal constituent melting at less than 1550°C
    • B23K35/3006Ag as the principal constituent

Landscapes

  • Engineering & Computer Science (AREA)
  • Mechanical Engineering (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、セラミツクスと金属をろう付けする
ためのろうの改良に係り、詳しくはろう付けし室
温に下げてくる時にセラミツクスに圧縮応力が加
わつて損傷するのを防止するため、熱応力を緩和
するクラツドろうに関する。 (従来の技術) 近年、各種のセラミツクス材料が、優れた耐熱
性、耐摩耗性等金属に無い特性を示すので、多方
面に利用され始めている。セラミツクス単体で形
成されている部品もあるが、多くはセラミツクス
の特長と金属の特長を生かす必要がある。そのた
めセラミツクスと金属の接合が要求される。セラ
ミツクスと金属は、夫々異なつた原子結合を有
し、一般のろう材では直接接合できない。良好に
接合するろう材としては、活性金属を含むろう材
が知られている。活性金属としてはTi、Zrがセ
ラミツクスと金属の接合に有効であるが、Ti、
Zr単体では融点が高い(Ti1720℃、Zr1860℃)
ので、通常Cu、Ni等と合金させ、融点を下げて
使用している。 (発明が解決しようとする問題点) ところで、前記のTi、Zr等にCu、Ni等を合金
させたろう材で、セラミツクスと金属をろう付け
することはできるが、ろう付け温度が高いので、
セラミツクスは応力によりクラツクが発生する欠
点があつた。クラツクの発生原因は、セラミツク
と金属との熱膨張差に起因するものであり、とり
わけSiC、Si3N4のような非酸化物系セラミツク
スとステンレス鋼、Cu、Feのような金属とは極
めて熱膨張差が大きいので、これを前記のTi、
Zr等にCu、Ni等を合金させたろう材でろう付け
すると、ろう付け時にはセラミツクスの膨張に比
しステンレス鋼が大きく膨張した状態でろう付け
され、これを室温に下げてくるとセラミツクスの
収縮に比しステンレス鋼の収縮が大きく、この差
に起因する応力によりクラツクが入つてしまうも
のである。 そこで本発明は、セラミツクスと金属をろう付
けした後の応力の緩和と強固な接合を可能ならし
めることのできる活性金属を含んだクラツドろう
を提供しようとするものである。 (問題点を解決するための手段) 上記問題点を解決するための本発明のクラツド
ろうの1つは、熱膨張係数の小さい金属又は合金
を中間材として、一面に活性金属を0.5〜8wt%含
有したAgろうが、他面に前記Agろうの融点に近
いAgろうが張られ、液相線温度が850℃以下であ
ることを特徴とするものである。 本発明のクラツドろうの他の1つは、熱膨張係
数の小さい金属又は合金を中間材として3層以内
とし、その中間材同志の間に活性金属を0.5〜8wt
%含有したAgろうの融点に近いAgろうが挿入さ
れ、最外側の一面に活性金属を0.5〜8wt%含有し
たAgろうが、最外側の他面に活性金属を0.5〜
8wt%含有したAgろうの融点に近いAgろうが張
られていることを特徴とするものである。 本発明のクラツドろうのさらに他の1つは、中
間材を2層又は3層とし、その内の外側から1層
又は2層が熱膨張係数の小さい金属又は合金で、
残りの1層又は2層がCu、Cu合金、Ag、Ag合
金、Ni、Ni合金のいずれかで、これら2層又は
3層の中間材同志の間に活性金属を0.5〜8wt%含
有したAgろうの融点に近いAgろうが挿入され、
前記熱膨張係数の小さい金属又は合金の中間材側
の最外側の一面に活性金属を0.5〜8wt%含有した
Agろうが、最外側の他面に前記最外側の一面の
Agろうの融点に近いAgろうが張られていること
を特徴とするものである。 本発明のクラツドろうの1つに於いて、中間材
に熱膨張係数の小さい金属又は合金を用いている
理由は、セラミツクスのとの熱膨張差を小さくし
てろう付け後の応力を緩和し、セラミツクスと金
属の良好な接合をなし得るためである。 また中間材の一面に、活性金属を0.5〜8wt%含
有したAgろうを張る理由は、加工性を向上させ、
強度アツプを図る為で、活性金属0.5wt%未満の
Agろうではセラミツクスに対する濡れ性が劣り、
且つ強度が不足し、活性金属が8wt%を超える
Agろうでは、ろう材の加工性が劣り、且つCu−
Ti合金の偏析が生じ、その上ろうの融点が上昇
するものであり、しかもろう付けに於いてろうの
じん性が無くなり、セラミツクスのクラツク発生
の原因となるからである。 さらに中間材の他面は、前記活性金属を0.5〜
8wt%含有したAgろうの融点に近いAgろうを張
る理由は、活性金属を含有するAgろうよりも金
属に対して濡れ性が良く、且つ継手強度が向上す
るからである。 また液相線温度を850℃以下とした理由は、ろ
う付け後のセラミツクスに掛かる応力を極力少な
くするためである。 本発明のクラツドろうの他の1つに於いて、中
間材を2層或いは3層とする理由は、セラミツク
スと金属の接合を一層良好にできるからで4層以
上にしてそれ以上接合効果は上がらず、コストが
高くなるだけであるからである。また中間材同志
の間に、活性金属を0.5〜8wt%含有したAgろう
の融点に近いAgろうを挿入した理由は、中間材
が2層或いは3層でもセラミツクスとの応力を緩
和する為である。最外側の両面に張られた材料
は、前記のクラツドろうの場合と同じ理由により
限定したものである。 本発明のクラツドろうのさらに他の1つに於い
て、中間材を2層又は3層とし、活性金属を0.5
〜8wt%含有したAgろう側の1層又は2層を熱
膨張係数の小さい金属又は合金とした理由は、セ
ラミツクスと熱膨張差を小さくしてろう付け後の
セラミツクスに掛かる応力を緩和するためであ
る。また中間材の他の1層または2層をCu、Cu
合金、Ag、Ag合金、Ni、Ni合金のいずれかと
した理由は第1層の中間材により応力の緩和があ
る程度達成されるので、これらの金属でも十分間
に合うからである。 本発明の中間材としての熱膨張係数の小さい金
属又は合金は、コバール、Fe−Ni42wt%、Fe−
Ni42wt%−Cr6wt%、Ta、Nb、Mo等で好まし
くは熱膨張係数が900℃以下で10×10-6/℃以下
のものである。 本発明のクラツドろうで接合できるセラミツク
スは、酸化物系(Al2O3など)、炭化物系(SiCな
ど)、窒化物系(Si3N4など)の各種セラミツク
スがある。また金属としては、融点が850℃を超
える金属ならCu系、Fe系、ステンレス鋼等広範
囲の金属と接合できる。 (実施例) 本発明によるクラツドろうの実施例を従来例と
共に説明する下記の表−1に示す成分組成の活性
金属を含むAgろう、中間材、Agろう、中間材、
Agろうを夫々真空溶解し、活性金属を含むAgろ
うは圧延して厚さ3mmの板となし、Agろうも同
様に圧延して3mmの板となし、中間材は同様に圧
延して厚さ6mmの板となした。そして実施例1、
5は第1図のように活性金属を含むAgろうの板
1、中間材の板2、Agろうの板3を重ね合わせ、
実施例2、4、6は第2図のように活性金属を含
むAgろうの板1、中間材の板2、Agろうの板
3、中間材の板2、Agろうの板3を重ね合わせ、
実施例3、7、8は第3図のように活性金属を含
むAgろうの板1、中間材の板2、Agろうの板
3、中間材の板2、Agろうの板3、中間材の板
2、Agろうの板3を重ね合わせ、夫々熱間中で
加圧圧着した。さらにテープ材にて熱間ロール圧
着した。この圧着したクラツドろう材を厚さ0.1
mmに圧延した。 尚、従来例1、2の活性金属を含むAgろうの
板1は厚さ3mmから厚さ0.1mmまで圧延した。
(Industrial Application Field) The present invention relates to the improvement of a solder for brazing ceramics and metal, and more specifically, to prevent damage due to compressive stress being applied to ceramics during brazing and cooling to room temperature. Therefore, it is related to clad solder which relieves thermal stress. (Prior Art) In recent years, various ceramic materials have begun to be used in a wide variety of fields because they exhibit properties that metals do not have, such as excellent heat resistance and wear resistance. Although some parts are made from ceramic alone, many require the use of the characteristics of ceramics and metals. Therefore, bonding between ceramics and metal is required. Ceramics and metals have different atomic bonds, and cannot be directly bonded using general brazing filler metals. A brazing filler metal containing an active metal is known as a brazing filler metal that provides good bonding. As active metals, Ti and Zr are effective for joining ceramics and metals, but Ti,
Zr alone has a high melting point (Ti 1720℃, Zr 1860℃)
Therefore, it is usually used by alloying it with Cu, Ni, etc. to lower its melting point. (Problems to be Solved by the Invention) By the way, ceramics and metal can be brazed using a brazing filler metal made by alloying Ti, Zr, etc. with Cu, Ni, etc., but since the brazing temperature is high,
Ceramics had the disadvantage of cracking due to stress. The cause of cracks is due to the difference in thermal expansion between ceramics and metals. In particular, non-oxide ceramics such as SiC and Si 3 N 4 and metals such as stainless steel, Cu, and Fe are extremely Since the difference in thermal expansion is large, this is compared to the above-mentioned Ti,
When brazing with a brazing filler metal made by alloying Zr, etc. with Cu, Ni, etc., the stainless steel expands significantly compared to the expansion of the ceramics during brazing, and when this is cooled to room temperature, the ceramics shrink. In comparison, stainless steel shrinks more, and the stress caused by this difference can cause cracks. SUMMARY OF THE INVENTION Therefore, the present invention provides a clad solder containing an active metal that can relieve stress and ensure strong bonding after brazing ceramics and metals. (Means for Solving the Problems) One of the clad solders of the present invention for solving the above problems uses a metal or alloy with a small coefficient of thermal expansion as an intermediate material, and contains 0.5 to 8 wt% of active metal on one side. The Ag solder contained therein is characterized in that an Ag solder having a melting point close to that of the Ag solder is applied on the other side, and the liquidus temperature is 850° C. or less. Another method of the clad solder of the present invention is to have up to three layers of a metal or alloy with a small coefficient of thermal expansion as an intermediate material, and 0.5 to 8 wt of active metal between the intermediate materials.
Ag solder containing 0.5 to 8 wt % of active metal is inserted on one outermost surface, and Ag solder containing 0.5 to 8 wt % of active metal is inserted on the other outermost surface.
It is characterized by being covered with Ag wax that has a melting point close to that of Ag wax containing 8wt%. Still another one of the clad solders of the present invention has two or three layers of intermediate material, of which one or two layers from the outside are made of a metal or alloy with a small coefficient of thermal expansion,
The remaining one or two layers are either Cu, Cu alloy, Ag, Ag alloy, Ni, or Ni alloy, and the intermediate material between these two or three layers is Ag containing 0.5 to 8 wt% of active metal. Ag wax with a melting point close to the wax is inserted,
0.5 to 8 wt% of active metal is contained on the outermost surface of the intermediate material side of the metal or alloy with a small coefficient of thermal expansion.
Ag solder is placed on the other outermost surface of the outermost surface.
It is characterized by being covered with Ag wax, which has a melting point close to that of Ag wax. In one of the clad solders of the present invention, a metal or alloy with a small thermal expansion coefficient is used as an intermediate material because it reduces the difference in thermal expansion with ceramics and relieves stress after brazing. This is because good bonding between ceramics and metal can be achieved. In addition, the reason for applying Ag solder containing 0.5 to 8 wt% of active metals on one side of the intermediate material is to improve workability.
In order to increase strength, active metal content of less than 0.5wt%
Ag wax has poor wettability to ceramics,
In addition, the strength is insufficient and the active metal content exceeds 8wt%.
With Ag brazing, the workability of the brazing metal is poor, and Cu-
This is because segregation of the Ti alloy occurs, and in addition, the melting point of the solder increases, and the solder loses its toughness during brazing, causing cracks in ceramics. Furthermore, the other side of the intermediate material contains the active metal in a range of 0.5 to 0.
The reason why Ag solder having a melting point close to that of Ag solder containing 8 wt% is used is that it has better wettability to the metal and improves joint strength than Ag solder containing active metals. The reason why the liquidus temperature was set to 850°C or less was to minimize the stress applied to the ceramics after brazing. The reason why the intermediate material is made of two or three layers in another method of the clad solder of the present invention is that the bond between the ceramic and the metal can be made even better, and the bonding effect cannot be further improved by using four or more layers. This is because the cost will only increase. Furthermore, the reason why Ag solder containing 0.5 to 8 wt% of active metal and having a melting point close to that of Ag solder is inserted between the intermediate materials is to alleviate the stress between the intermediate materials and the ceramics even if the intermediate materials have two or three layers. . The material applied to the outermost surfaces is limited for the same reasons as in the case of the clad solder described above. In yet another Clad solder of the present invention, the intermediate material is two or three layers, and the active metal is 0.5
The reason why one or two layers on the brazing side of Ag containing ~8wt% is made of a metal or alloy with a small coefficient of thermal expansion is to reduce the difference in thermal expansion with ceramics and alleviate the stress applied to the ceramics after brazing. be. In addition, the other one or two layers of the intermediate material are Cu, Cu.
The reason for selecting Ag, Ag alloy, Ni, or Ni alloy is that stress relaxation can be achieved to some extent by the intermediate material of the first layer, so these metals can also suffice. Metals or alloys with a small coefficient of thermal expansion as intermediate materials of the present invention include Kovar, Fe-Ni42wt%, Fe-
Ni42wt%-Cr6wt%, Ta, Nb, Mo, etc., preferably have a thermal expansion coefficient of 900°C or less and 10×10 -6 /°C or less. Ceramics that can be bonded using the clad solder of the present invention include various types of oxide-based (such as Al 2 O 3 ), carbide-based (such as SiC), and nitride-based (such as Si 3 N 4 ) ceramics. In addition, it can be bonded to a wide range of metals with a melting point of over 850°C, such as Cu-based, Fe-based, and stainless steel. (Example) An example of a clad solder according to the present invention will be explained together with a conventional example. Ag solder, intermediate material, Ag solder, intermediate material, containing an active metal having the composition shown in Table 1 below.
The Ag solder is melted in vacuum, the Ag solder containing active metal is rolled into a 3 mm thick plate, the Ag solder is similarly rolled into a 3 mm thick plate, and the intermediate material is rolled in the same way to make a 3 mm thick plate. It was made into a 6mm plate. And Example 1,
As shown in Fig. 1, 5 is made by overlapping Ag solder plate 1 containing active metal, intermediate material plate 2, and Ag solder plate 3.
In Examples 2, 4, and 6, as shown in Fig. 2, Ag solder plate 1 containing active metal, intermediate material plate 2, Ag solder plate 3, intermediate material plate 2, and Ag solder plate 3 are stacked together. ,
Examples 3, 7, and 8 are as shown in Fig. 3, including an active metal-containing Ag solder plate 1, intermediate material plate 2, Ag solder plate 3, intermediate material plate 2, Ag solder plate 3, and intermediate material. Plate 2 and Ag solder plate 3 were stacked on top of each other and bonded under pressure in a hot environment. Furthermore, hot roll pressure bonding was performed using tape material. This crimped crud filler metal has a thickness of 0.1
Rolled to mm. The active metal-containing Ag brazing plate 1 of Conventional Examples 1 and 2 was rolled from a thickness of 3 mm to a thickness of 0.1 mm.

【表】 然して実施例1〜8及び従来例1、2のろう材
を夫々縦横5mm、15mm、40mmの各寸法に切断し
て、これらのろうを用いてセラミツクスと金属の
ろう付け、本例では共に厚さ5mmのAl2O3とCu及
びSUS304のろう付けをArガス雰囲気炉で行い、
ろう付け部のセラミツクス即ちAl2O3の割れを調
べた処、下記の表−2に示すような結果を得た。
尚、実施例の各クラツドろうは、活性金属を含む
Agろう側をセラミツクス側に配してろう付けを
行つた。
[Table] However, the brazing materials of Examples 1 to 8 and Conventional Examples 1 and 2 were cut into length and width dimensions of 5 mm, 15 mm, and 40 mm, respectively, and these solders were used to braze ceramics and metal, in this example. Brazing of Al 2 O 3 , Cu and SUS304 with a thickness of 5 mm was performed in an Ar gas atmosphere furnace.
When we investigated cracks in the ceramics, ie, Al 2 O 3 at the brazed part, we obtained the results shown in Table 2 below.
In addition, each of the clad solders in the examples contains an active metal.
Brazing was performed with the Ag solder side placed on the ceramic side.

【表】 ○…割れ無し、×…割れる。
上記の表−2で明らかなように本発明の実施例
のクラツドろうによれば、Al2O3とCuのろう付け
に於いてAl2O3は全く割れることが無く、Al2O3
とSUS304のろう付けに於いてもAl2O3が割れる
ことが少なく、僅かに中間材が1層及び2層で、
ろう付け寸法の大きいものに於いて割れが見られ
る程度で、中間材が3層の実施例3、7、8のク
ラツドろうによるろう付けの場合は全く割れるこ
とが無かつた。 (発明の効果) 以上詳細した通り本発明のクラツドろうは、セ
ラミツクスと金属のろう付けに於いて、セラミツ
クスに対する応力を緩和してセラミツクスが応力
によりクラツクが入つて損傷するのを防止でき、
しかもセラミツクスと金属を強固にろう付けして
接合できるので、従来のろうけとによつて代わる
ことのできる画期的なものと云える。
[Table] ○…No cracking, ×…Cracked.
As is clear from Table 2 above, according to the clad solder according to the embodiment of the present invention, Al 2 O 3 does not crack at all when Al 2 O 3 and Cu are brazed, and Al 2 O 3
Even when brazing SUS304, Al 2 O 3 rarely cracks, and only one and two layers of intermediate material are used.
Cracks were only observed when the brazing size was large, but there was no cracking at all in the case of brazing using clad brazing in Examples 3, 7, and 8, in which the intermediate material was three layers. (Effects of the Invention) As detailed above, the solder solder of the present invention can prevent the ceramic from cracking and being damaged due to stress by relieving the stress on the ceramic when brazing ceramics and metal.
Moreover, it can be said to be an epoch-making product that can replace conventional soldering because ceramics and metal can be firmly joined by brazing.

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

第1図乃至第3図は夫々本発明のクラツドろう
を作る際の素材の重ね合わせ状態を示す斜視図で
ある。
FIGS. 1 to 3 are perspective views showing the overlapping state of materials when making the clad solder of the present invention.

Claims (1)

【特許請求の範囲】 1 熱膨張係数の小さい金属又は合金を中間材と
して、一面に活性金属を0.5〜8wt%含有したAg
ろうが、他面に前記Agろうの融点に近いAgろう
が張られ、液相線温度が850℃以下であることを
特徴とするクラツドろう。 2 熱膨張係数の小さい金属又は合金を中間材と
して3層以内とし、その中間材同志の間に活性金
属を0.5〜8wt%含有したAgろうの融点に近いAg
ろうが挿入され、最外側の一面に活性金属を0.5
〜8wt%含有したAgろうが、最外側の他面に活
性金属を0.5〜8wt%含有したAgろうの融点に近
いAgろうが張られていることを特徴とするクラ
ツドろう。 3 中間材を2層又は3層とし、その内の外側か
ら1層又は2層が熱膨張係数の小さい金属又は合
金で残りの1層又は2層がCu、Cu合金、Ag、
Ag合金、Ni、Ni合金のいずれかで、これら2層
又は3層の中間材同志の間に活性金属を0.5〜8wt
%含有したAgろうの融点に近いAgろうが挿入さ
れ、前記熱膨張係数の小さい金属又は合金の中間
材側の最外側の一面に活性金属を0.5〜8wt%含有
したAgろうが、最外側の他面に前記最外側の一
面のAgろうの融点に近いAgろうが張られている
ことを特徴とするクラツドろう。
[Claims] 1. Ag containing 0.5 to 8 wt% of active metal on one side using a metal or alloy with a small coefficient of thermal expansion as an intermediate material.
A clad solder characterized in that the other side of the solder is coated with Ag solder having a melting point close to that of the Ag solder, and whose liquidus temperature is 850°C or less. 2 Up to three layers of metal or alloy with a small coefficient of thermal expansion are used as an intermediate material, and Ag close to the melting point of Ag solder containing 0.5 to 8 wt% of active metal between the intermediate materials.
The wax is inserted and the active metal is applied to the outermost side by 0.5
A cladding solder characterized in that an Ag solder containing ~8wt% is covered with an Ag solder having a melting point close to that of the Ag solder containing an active metal of 0.5~8wt% on the other outermost surface. 3 The intermediate material is made of two or three layers, of which one or two layers from the outside are metals or alloys with a small coefficient of thermal expansion, and the remaining one or two layers are made of Cu, Cu alloy, Ag,
Ag alloy, Ni, or Ni alloy, with 0.5 to 8wt of active metal between these two or three layers of intermediate material.
Ag solder containing 0.5 to 8 wt% of active metal is inserted into the outermost surface of the intermediate material side of the metal or alloy with a small thermal expansion coefficient, and the Ag solder containing 0.5 to 8 wt% of active metal A clad solder characterized in that the other surface is covered with Ag solder having a melting point close to that of the Ag solder on the outermost surface.
JP1146086A 1986-01-22 1986-01-22 Cladding solder Granted JPS62168694A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP1146086A JPS62168694A (en) 1986-01-22 1986-01-22 Cladding solder

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP1146086A JPS62168694A (en) 1986-01-22 1986-01-22 Cladding solder

Publications (2)

Publication Number Publication Date
JPS62168694A JPS62168694A (en) 1987-07-24
JPH0526599B2 true JPH0526599B2 (en) 1993-04-16

Family

ID=11778704

Family Applications (1)

Application Number Title Priority Date Filing Date
JP1146086A Granted JPS62168694A (en) 1986-01-22 1986-01-22 Cladding solder

Country Status (1)

Country Link
JP (1) JPS62168694A (en)

Families Citing this family (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS63248780A (en) * 1987-04-02 1988-10-17 株式会社東芝 Ceramic structure
JPH02217191A (en) * 1989-02-16 1990-08-29 Tanaka Kikinzoku Kogyo Kk Clad brazing material for ceramics
JP2594475B2 (en) * 1990-04-16 1997-03-26 電気化学工業株式会社 Ceramic circuit board
JPH09181423A (en) * 1990-04-16 1997-07-11 Denki Kagaku Kogyo Kk Ceramic circuit board
JPH07108474B2 (en) * 1992-01-16 1995-11-22 スカイアルミニウム株式会社 Brazing sheet and brazing method using the same

Also Published As

Publication number Publication date
JPS62168694A (en) 1987-07-24

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