JPH01154898A - Solder - Google Patents

Solder

Info

Publication number
JPH01154898A
JPH01154898A JP31562887A JP31562887A JPH01154898A JP H01154898 A JPH01154898 A JP H01154898A JP 31562887 A JP31562887 A JP 31562887A JP 31562887 A JP31562887 A JP 31562887A JP H01154898 A JPH01154898 A JP H01154898A
Authority
JP
Japan
Prior art keywords
brazing
hydride
metal
solder
powdery
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.)
Granted
Application number
JP31562887A
Other languages
Japanese (ja)
Other versions
JP2532114B2 (en
Inventor
Shigeo Shioda
重雄 塩田
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 JP62315628A priority Critical patent/JP2532114B2/en
Publication of JPH01154898A publication Critical patent/JPH01154898A/en
Application granted granted Critical
Publication of JP2532114B2 publication Critical patent/JP2532114B2/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

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Abstract

PURPOSE:To obtain the title solder having a low brazing temp. and capable of obtaining high brazed joint strength by kneading a mixture of powdery Ag and Cu and the powdery hydride of a specified metal with a binder. CONSTITUTION:A mixed powdery solder component consisting of 47.6-85.7wt.% powdery Ag, 4.8-19wt.% of at least one kind among Ti hydride, Zr hydride, and Hf hydride, and the balance Cu powder and an org. binder are mixed in 1/3-3/1 ratio to obtain the solder. By using the obtained solder, a ceramic is brazed to a ceramic, a ceramic to a metal, and a metal to a metal with high brazing strength.

Description

【発明の詳細な説明】 (産業上の利用分野) 本発明は、セラミックスとセラミックス、セラミックス
と金属、金属と金属を接合する為のろう材に関するもの
である。
DETAILED DESCRIPTION OF THE INVENTION (Field of Industrial Application) The present invention relates to a brazing material for joining ceramics to ceramics, ceramics to metals, and metals to metals.

(従来技術とその問題点) 従来よりセラミックスと金属の接合方法としては、一般
に酸化ソルダー法、テレフンケン法、活性金属法などが
ある。
(Prior Art and its Problems) Conventional methods for joining ceramics and metals include the oxidation solder method, the Telefunken method, and the active metal method.

活性金属法とは、非常に活性な金属、Ti、Zr等と、
これらと比較的低融点の合金を作るNi、Crとを共晶
組成になるようしたろう材をセラミックスと金属の間に
挿入して真空中又は不活性ガス中で接合する方法である
The active metal method refers to the use of very active metals such as Ti, Zr, etc.
In this method, a brazing filler metal having a eutectic composition of Ni and Cr, which form an alloy with a relatively low melting point, is inserted between the ceramic and the metal, and the bonding is performed in a vacuum or in an inert gas.

ところで、前記金属の共晶温度は、Cr、Ti34重量
%で880°C,T i −N i24.5重量%で9
55°Cであるので、高温で接合しなければならない。
Incidentally, the eutectic temperature of the metals is 880°C when Cr and Ti are 34% by weight, and 9°C when Ti-Ni is 24.5% by weight.
Since the temperature is 55°C, bonding must be performed at a high temperature.

また高温で接合するので、熱膨張も大きくなる。Furthermore, since bonding is carried out at high temperatures, thermal expansion also increases.

このように従来の活性金属法で用いるろう材のろう付温
度は、900°C以上の高温となるので、エネルギーの
損失、金属母材の軟化、熱膨張率が高い等の問題があっ
た。
As described above, the brazing temperature of the brazing material used in the conventional active metal method is a high temperature of 900° C. or higher, which causes problems such as energy loss, softening of the metal base material, and high coefficient of thermal expansion.

このような問題解決のためにAg−Cu−(Ti、Zr
、Hf)等の低温ろう材が開発された。継手形状が複雑
なものについては、板とか線状のろう材のかわりに粉末
ろうが多く利用されている。しかしAg−Cu−(Ti
、Zr、Hf)のアトマイズ粉を製造するには、活性金
属を酸化させないためにアトマイズ装置全体を高真空に
保たなければならず生産性に問題がある。この問題を解
決するためにAg粉とCu粉もしくはAg、Cu合金粉
にTi、Zr、Hfの粉末を混合する方法が行われてい
る。しかしこの方法であると、Ti、Zr、Hfの粉末
表面が酸化被膜で覆われておりろう付強度が十分でなく
、使用に供することができない。
To solve this problem, Ag-Cu-(Ti, Zr
, Hf) and other low-temperature brazing fillers have been developed. For joints with complex shapes, powdered solder is often used instead of plate or wire brazing material. However, Ag-Cu-(Ti
, Zr, Hf), the entire atomizing device must be kept in a high vacuum to prevent the active metal from oxidizing, which poses a problem in productivity. In order to solve this problem, a method of mixing Ti, Zr, and Hf powders with Ag powder and Cu powder or Ag and Cu alloy powder has been used. However, with this method, the surfaces of the Ti, Zr, and Hf powders are covered with an oxide film, and the brazing strength is insufficient, so that the powders cannot be used.

(発明の目的) 本発明は上記の問題を解決すべくなされたもので、ろう
付温度が低く且つろう付継手強度を高くできるろう材を
提供することを目的とするものである。
(Object of the Invention) The present invention was made to solve the above-mentioned problems, and an object of the present invention is to provide a brazing material that can be used at a low brazing temperature and that can increase the strength of a brazed joint.

(問題点を解決するための手段) 本発明のろう材は、Ag47.6〜85.7重量%、T
i水素化物、Zr水素化物、Hf水素化物の少なくとも
1種4.8〜19重量%、残部Cuから成る粉末状ろう
成分とバインダー成分から成るものである。
(Means for solving the problem) The brazing filler metal of the present invention contains 47.6 to 85.7% by weight of Ag, T
It consists of a powdery wax component consisting of 4.8 to 19% by weight of at least one of i hydride, Zr hydride, and Hf hydride, and the balance Cu, and a binder component.

本発明のろう材に於いて、Ti5Zr、Hfの水素化物
を利用した理由は、水素化物が600’C以下では非常
に安定であり、酸化皮膜を形成しないため、ろう伸直前
まで表面清浄であり、ろう付性に有効であるからである
The reason why hydrides of Ti5Zr and Hf are used in the brazing material of the present invention is that hydrides are very stable below 600'C and do not form an oxide film, so the surface can be kept clean until just before the solder is stretched. This is because it is effective for brazing properties.

ろう付温度においては、水素化物は分解し発生したH2
がろう付置囲気(通常は真空もしくは不活性)中の微量
の酸素と反応しろう付に最適な雰囲気となる。
At the brazing temperature, the hydride decomposes and the generated H2
This reacts with trace amounts of oxygen in the brazing atmosphere (usually vacuum or inert), creating the perfect atmosphere for brazing.

また水素化物は金属粉末製造の前工程で生産されるもの
で価格的にも安価である効果がある。
In addition, hydrides are produced in the pre-process of producing metal powder, and have the advantage of being inexpensive.

(実施例) 本発明のろう材の具体的な実施例を従来例と共に説明す
る。
(Example) Specific examples of the brazing filler metal of the present invention will be described together with conventional examples.

下記の表−1に示す成分組成の実施例1〜3のろう材は
、アトマイズ法により作成したAg粉およびCu粉と水
素化物を混合したものおよびアトマイズ法により作成し
たAg、Cu合金粉に水素化物を混合したものに有機バ
インダーを混練したものである。従来例1.2のろう材
は同じくアトマイズ法により作成したAg粉及びCu粉
もしくはAg、Cu合金粉に水素化物を分解して得たT
i粉もしくはZn粉を混合したものに有機バインダーを
混練したものである。
The brazing filler metals of Examples 1 to 3 with the component compositions shown in Table 1 below are mixtures of Ag powder and Cu powder created by the atomization method and hydrides, and Ag and Cu alloy powder created by the atomization method mixed with hydrogen. It is made by kneading an organic binder into a mixture of chemical compounds. The brazing filler metal of Conventional Example 1.2 is T obtained by decomposing a hydride into Ag powder and Cu powder or Ag and Cu alloy powder, which were also created by the atomization method.
An organic binder is kneaded into a mixture of I powder or Zn powder.

(以下余白) 各ろう材をセラミックスとセラミックス、セラミックス
とFe−Ni42重量%合金と継手部に塗布してろう付
を行った。そしてそれらのろう付継手の剪断試験とを行
った処、下記の表−2に示すような結果を得た。
(The following is a blank space) Each brazing filler metal was applied to ceramics and ceramics, and ceramics and Fe-Ni 42 weight% alloy, and joint parts, and brazing was performed. When these brazed joints were subjected to a shear test, the results shown in Table 2 below were obtained.

表−2 上記の表−2で明らかなように実施例1〜3のろう材は
、従来例1.2のろう材に比しろう付強度も著しく高い
ことが判る。
Table 2 As is clear from Table 2 above, the brazing strength of the brazing fillers of Examples 1 to 3 is significantly higher than that of the brazing fillers of Conventional Examples 1 and 2.

尚、上記実施例では、ろう材とバインダーの比が2=1
であるが、本願発明はこれに限るものではなく、ろう材
としての使い勝手の面からろう材とバインダーの比は1
:3〜3:1が好ましい範囲である。
In the above embodiment, the ratio of brazing material to binder is 2=1.
However, the present invention is not limited to this, and from the viewpoint of ease of use as a brazing material, the ratio of the brazing material to the binder is 1.
:3 to 3:1 is a preferable range.

(発明の効果) 以上の通り本発明のろう材は、ろう付強度を高くできま
た価格的にも従来のろう材よりも有利であるので、従来
のろう材にとって代わることのできる画期的なものと云
える。
(Effects of the Invention) As described above, the brazing filler metal of the present invention can increase brazing strength and is more cost-effective than conventional brazing filler metals, so it is a revolutionary material that can replace conventional brazing filler metals. It can be said that it is a thing.

出願人  田中貴金属工業株式会社Applicant: Tanaka Kikinzoku Kogyo Co., Ltd.

Claims (1)

【特許請求の範囲】[Claims] Ag47.6〜85.7重量%、Ti水素化物、Zr水
素化物、Hf水素化物の少なくとも1種4.8〜19重
量%、残部Cuから成る粉末状ろう成分とバインダー成
分から成るろう材。
A brazing material consisting of a powdery brazing component consisting of 47.6 to 85.7% by weight of Ag, 4.8 to 19% by weight of at least one of Ti hydride, Zr hydride, and Hf hydride, and the balance Cu, and a binder component.
JP62315628A 1987-12-14 1987-12-14 Brazing material Expired - Lifetime JP2532114B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP62315628A JP2532114B2 (en) 1987-12-14 1987-12-14 Brazing material

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP62315628A JP2532114B2 (en) 1987-12-14 1987-12-14 Brazing material

Publications (2)

Publication Number Publication Date
JPH01154898A true JPH01154898A (en) 1989-06-16
JP2532114B2 JP2532114B2 (en) 1996-09-11

Family

ID=18067653

Family Applications (1)

Application Number Title Priority Date Filing Date
JP62315628A Expired - Lifetime JP2532114B2 (en) 1987-12-14 1987-12-14 Brazing material

Country Status (1)

Country Link
JP (1) JP2532114B2 (en)

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH04168792A (en) * 1990-11-01 1992-06-16 Kawasaki Steel Corp Manufacture of high heat radiating ceramic circuit board with excellent thermal shock resistance
JPH07276076A (en) * 1994-04-08 1995-10-24 Matsushita Electric Ind Co Ltd Cream solder
CN107322187A (en) * 2017-09-05 2017-11-07 广州先艺电子科技有限公司 A kind of active soldering paste of silver-bearing copper titanium
CN113976877A (en) * 2021-12-29 2022-01-28 广州先艺电子科技有限公司 Metal composition for preparing AgCuTi soldering lug, soldering lug and preparation method of soldering lug

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS59141465A (en) * 1983-01-31 1984-08-14 三井造船株式会社 Solder
JPS59141393A (en) * 1983-01-31 1984-08-14 Mitsui Eng & Shipbuild Co Ltd Brazing filler material
JPS60130494A (en) * 1983-12-16 1985-07-11 Kitsudo:Kk Conductive paste for die bonding

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS59141465A (en) * 1983-01-31 1984-08-14 三井造船株式会社 Solder
JPS59141393A (en) * 1983-01-31 1984-08-14 Mitsui Eng & Shipbuild Co Ltd Brazing filler material
JPS60130494A (en) * 1983-12-16 1985-07-11 Kitsudo:Kk Conductive paste for die bonding

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH04168792A (en) * 1990-11-01 1992-06-16 Kawasaki Steel Corp Manufacture of high heat radiating ceramic circuit board with excellent thermal shock resistance
JPH07276076A (en) * 1994-04-08 1995-10-24 Matsushita Electric Ind Co Ltd Cream solder
CN107322187A (en) * 2017-09-05 2017-11-07 广州先艺电子科技有限公司 A kind of active soldering paste of silver-bearing copper titanium
CN113976877A (en) * 2021-12-29 2022-01-28 广州先艺电子科技有限公司 Metal composition for preparing AgCuTi soldering lug, soldering lug and preparation method of soldering lug

Also Published As

Publication number Publication date
JP2532114B2 (en) 1996-09-11

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