JPH0446695A - Brazing filler metal for brazing to aluminum member - Google Patents
Brazing filler metal for brazing to aluminum memberInfo
- Publication number
- JPH0446695A JPH0446695A JP15612190A JP15612190A JPH0446695A JP H0446695 A JPH0446695 A JP H0446695A JP 15612190 A JP15612190 A JP 15612190A JP 15612190 A JP15612190 A JP 15612190A JP H0446695 A JPH0446695 A JP H0446695A
- Authority
- JP
- Japan
- Prior art keywords
- brazing
- aluminum
- filler metal
- brazing filler
- aluminum member
- 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
Links
- 238000005219 brazing Methods 0.000 title claims abstract description 96
- 229910052782 aluminium Inorganic materials 0.000 title claims abstract description 49
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 title claims abstract description 48
- 239000000945 filler Substances 0.000 title claims description 42
- 229910052751 metal Inorganic materials 0.000 title claims description 42
- 239000002184 metal Substances 0.000 title claims description 42
- 239000011701 zinc Substances 0.000 claims abstract description 24
- 229910052710 silicon Inorganic materials 0.000 claims abstract description 16
- 239000010703 silicon Substances 0.000 claims abstract description 16
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical group [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 claims abstract description 12
- 229910052725 zinc Inorganic materials 0.000 claims abstract description 12
- 239000012535 impurity Substances 0.000 claims abstract description 7
- 239000000463 material Substances 0.000 claims description 21
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 claims description 14
- 239000010949 copper Substances 0.000 claims description 13
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 claims description 11
- 229910052802 copper Inorganic materials 0.000 claims description 11
- AZDRQVAHHNSJOQ-UHFFFAOYSA-N alumane Chemical group [AlH3] AZDRQVAHHNSJOQ-UHFFFAOYSA-N 0.000 claims description 4
- 238000002844 melting Methods 0.000 abstract description 18
- 230000008018 melting Effects 0.000 abstract description 18
- 239000000203 mixture Substances 0.000 abstract description 7
- 229910000838 Al alloy Inorganic materials 0.000 abstract description 4
- 230000000052 comparative effect Effects 0.000 description 10
- 230000000694 effects Effects 0.000 description 7
- 239000000126 substance Substances 0.000 description 6
- 238000005260 corrosion Methods 0.000 description 5
- 230000007797 corrosion Effects 0.000 description 5
- 230000004907 flux Effects 0.000 description 4
- 150000002739 metals Chemical class 0.000 description 3
- 238000000034 method Methods 0.000 description 3
- 238000007747 plating Methods 0.000 description 3
- 238000011160 research Methods 0.000 description 2
- 125000006850 spacer group Chemical group 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
- KRHYYFGTRYWZRS-UHFFFAOYSA-M Fluoride anion Chemical compound [F-] KRHYYFGTRYWZRS-UHFFFAOYSA-M 0.000 description 1
- 241000102542 Kara Species 0.000 description 1
- 229910013470 LiC1 Inorganic materials 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 230000002950 deficient Effects 0.000 description 1
- 230000002542 deteriorative effect Effects 0.000 description 1
- 230000003628 erosive effect Effects 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 238000001192 hot extrusion Methods 0.000 description 1
- 239000011261 inert gas Substances 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 238000005096 rolling process Methods 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- JBQYATWDVHIOAR-UHFFFAOYSA-N tellanylidenegermanium Chemical compound [Te]=[Ge] JBQYATWDVHIOAR-UHFFFAOYSA-N 0.000 description 1
- 238000005491 wire drawing Methods 0.000 description 1
Landscapes
- Laminated Bodies (AREA)
- Ceramic Products (AREA)
Abstract
Description
【発明の詳細な説明】
〔産業上の利用分野〕
この発明は、アルミニウム部材またはアルミニウム合金
部材(以下、「アルミニウム部材」と総称する)をろう
付けするため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 brazing aluminum members or aluminum alloy members (hereinafter collectively referred to as "aluminum members").
近年、自動車用熱交換器、などに、アルミニウム部材が
広く使用されるようになってきた。このようなアルミニ
ウム部材の相互の接合は、一般に、Al1−3i系ろう
材を使用し、 次のようなろう付け法によって行なわれ
ている。In recent years, aluminum members have come to be widely used in automobile heat exchangers and the like. Such aluminum members are generally joined to each other by the following brazing method using an Al1-3i brazing filler metal.
a、真空炉内で行なうろう付け。a. Brazing performed in a vacuum furnace.
b、フッ化物系フラックスを使用し、不活性雰囲気下の
炉内で行なうろう付け、
C0塩化物系フラックスを使用し、大気下の炉内で行な
うろう付け。b. Brazing using fluoride-based flux in a furnace under an inert atmosphere; Brazing using CO chloride-based flux in a furnace under atmospheric air.
d、トーチを使用して行なうろう付け。d. Brazing performed using a torch.
上述した従来の方法によるろう付け温度は、何れも約6
00℃であって、アルミニウムの融点に近い、このため
に、ろう付け時に、アルミニウム部材が座屈しまたは溶
融するという問題が生ずる。The brazing temperature according to the conventional method described above is approximately 6
00° C., which is close to the melting point of aluminum, which causes the problem of buckling or melting of the aluminum parts during brazing.
一方、融点の低いろう材として、 Zn:100wt%
、または、Zn: 95wt、%とAll:5wt、%
とからなるZn系ろう材が知られている。 このような
Zn系ろう材を使用すれば、上述した問題は解決される
が、 その反面、Zn: 100wt、%のろう材は、
アルミニウム部材への侵食が大であり、そして、 Zn
:95wt、%とA II : 5wt、%とからなる
ろう材は、その表面に強固な酸化皮膜が生じて、ろう付
け性が低下し、接合部の品質が劣化する問題がある。On the other hand, as a brazing material with a low melting point, Zn: 100wt%
, or Zn: 95wt,% and All: 5wt,%
A Zn-based brazing filler metal consisting of the following is known. If such a Zn-based brazing filler metal is used, the above-mentioned problem will be solved, but on the other hand, a brazing filler metal with Zn: 100 wt.
The corrosion of aluminum parts is large, and Zn
A brazing filler metal consisting of A II : 95wt, % and A II : 5wt, % has the problem that a strong oxide film is formed on its surface, reducing brazing properties and deteriorating the quality of the joint.
上述した開運を解決するために、従来から種々研究が行
なわれており、例えば、次のろう材が提案されている。In order to solve the above-mentioned problem, various researches have been carried out in the past, and for example, the following brazing filler metals have been proposed.
(1)特公昭50−35018号公報に開示されている
、Zn:4〜10wt、%、Si:3〜6wt、%、残
り、アルミニウムおよび不可避的不純物、からなるろう
材(以下、「先行技術1)という)。(1) A brazing filler metal (hereinafter referred to as "prior art 1)).
(2)特開昭63−309391号公報に開示されてい
る、Zn:20〜80wt、%、si: 1〜11wt
、%、残り、アルミニウムおよび不可避的不純物、から
なるろう材、上述したろう材は、0.1〜Lowt、%
のCuを、更に付加的に含有゛していてもよい(以下、
「先行技術2」という)。(2) Zn: 20 to 80 wt, %, si: 1 to 11 wt, disclosed in Japanese Patent Application Laid-Open No. 63-309391
, %, remainder, aluminum and unavoidable impurities, the above-mentioned brazing filler metal has a content of 0.1 to Low, %
may additionally contain Cu (hereinafter referred to as
(referred to as "Prior Art 2").
先行技術lには1次に述べるような問題がある。 Prior art 1 has the following problems.
即ち、 Znの含有量が、4〜10wt、%の範囲内と
少ないので、このろう材のろう付け温度範囲は、アルミ
ニウム部材の固相線温度に近い。従って、アルミニウム
部材の固相線温度に近い高温度でろう付けする必要があ
り、アルミニウム部材が、溶融しまたは変形することが
ある。That is, since the Zn content is small within the range of 4 to 10 wt.%, the brazing temperature range of this brazing filler metal is close to the solidus temperature of the aluminum member. Therefore, it is necessary to braze at a high temperature close to the solidus temperature of the aluminum member, which may cause the aluminum member to melt or deform.
先行技術2には1次に述べるような問題がある。Prior art 2 has the following problems as described in the first section.
即ち、先行技術2のろう材は、20〜80%+1.%の
Zn、および、1〜111IIt0%のSiを含有して
いるので、約450〜570℃の温度でアルミニウム部
材をろう付けすることができる。しかしながら。That is, the brazing material of Prior Art 2 has a content of 20 to 80%+1. % of Zn and 1 to 111 IIt0% of Si, aluminum members can be brazed at a temperature of about 450 to 570°C. however.
近年多く使用されているJIS2000系のアルミニウ
ム部材の融点は、約520℃で低い、従って、先行技術
2のろう材によっても、このような低融点のアルミニウ
ム部材をろう付けするときには、ろう付け温度を厳しく
管理する必要がある。The melting point of JIS 2000 series aluminum members, which have been widely used in recent years, is as low as approximately 520°C. Therefore, even with the brazing filler metal of Prior Art 2, when brazing aluminum members with such a low melting point, the brazing temperature must be lowered. It needs to be strictly controlled.
このために、より低い温度でろう付けすることができ、
そして、ろう付け性に優れたろう材の開発が強く望まれ
ている。For this reason, it is possible to braze at lower temperatures,
There is a strong desire to develop a brazing filler metal with excellent brazing properties.
従って、この発明の目的は、低融点のアルミニウム部材
を、溶融や変形が生ずることなく、そして、能率的にろ
う付けすることができ、しかも、品質の優れた接合部が
得られる、ろう材を提供することにある。Therefore, an object of the present invention is to provide a brazing material that can efficiently braze low-melting-point aluminum members without melting or deforming them, and that can provide high-quality joints. It is about providing.
[課題を解決するための手段〕
本発明者等は、上述した問題を解決し、低融点のアルミ
ニウム部材を、溶融や変形が生ずることなく、そして、
能率的にろう付けすることができ、しかも、品質の優れ
た接合部が得られるろう材を開発すべく、鋭意研究を重
ねた。その結果、ろう付け温度が約380〜480℃の
ろう材は、上述した条件を満たすことができ、このよう
なろう材は、その成分組成を、85〜97wt、%の亜
鉛と。[Means for Solving the Problems] The present inventors have solved the above-mentioned problems, and have made an aluminum member with a low melting point without melting or deforming, and
We conducted extensive research in order to develop a brazing material that can be efficiently brazed and produce high-quality joints. As a result, a brazing filler metal whose brazing temperature is approximately 380 to 480°C can satisfy the above-mentioned conditions, and such a brazing filler metal has a component composition of 85 to 97 wt.% zinc.
0.3〜5wt、%のケイ素および/または2〜10w
t、%の銅と、残り、アルミニウムおよび不可避的不純
物に限定すれば得られることを知見した。0.3-5wt, % silicon and/or 2-10w
It has been found that it can be obtained by limiting the amount to t,% of copper and the rest to aluminum and unavoidable impurities.
この発明は、上記知見に基づいてなされたものであって
、この発明の、アルミニウム部材のろう付け用ろう材は
、
亜 鉛=85〜97wt、%。This invention has been made based on the above findings, and the brazing filler metal for brazing aluminum members according to the present invention has a zinc content of 85 to 97 wt%.
ケイ素二0.3〜5wt、嶌および銅: 2〜10wt
、%の少なくとも1つ、および、
残り、アルミニウムおよび不可避不純物からなることに
特徴を有するものである。Silicon 0.3-5wt, Shima and copper: 2-10wt
, %, and the remainder consists of aluminum and unavoidable impurities.
この発明のろう材の化学成分組成を、上述した範囲内に
限定した理由について、以下に述べる。The reason why the chemical composition of the brazing filler metal of this invention is limited to the above-mentioned range will be described below.
(1)亜鉛(Zn) 亜鉛には、ろう材の融点を下げる作用がある。(1) Zinc (Zn) Zinc has the effect of lowering the melting point of the brazing filler metal.
しかしながら、亜鉛含有量が85wt、%未満では、J
IS 2000系のアルミニウム合金製のような低融点
のアルミニウム部材を、溶融や変形が生ずることなくろ
う付けし得るように、 ろう付け温度を450℃以下に
下げることができない、一方、亜鉛含有量が97wt、
%を超えると、融解したろう材によってアルミニウム部
材が侵食される問題が生ずる。However, when the zinc content is less than 85 wt.%, J
The brazing temperature cannot be lowered below 450°C so that low melting point aluminum parts, such as those made of IS 2000 series aluminum alloys, can be brazed without melting or deformation. 97wt,
%, the problem arises that the aluminum member is eroded by the molten brazing filler metal.
従って、亜鉛含有量は、85から97wt、%の範囲内
に、そして、より好ましくは、90から95wt、%の
範囲内に限定すべきである。Therefore, the zinc content should be limited to within the range of 85 to 97 wt.%, and more preferably within the range of 90 to 95 wt.%.
(2)ケイ素(Si) 、銅(Cu)
ケイ素および銅には、ろう材の表面に生ずる酸化皮膜を
ポーラス状にすると共に、これを薄く保って破壊されや
すくなし、そして、ろう材の電気化学的性質を責となし
てその腐食を抑制し、更に、融解したろう材の流動性を
向上させる作用がある。(2) Silicon (Si), Copper (Cu) Silicon and copper are used to make the oxide film that forms on the surface of the brazing material porous, to keep it thin so that it is not easily destroyed, and to make the electrolytic film of the brazing material porous. It also has the effect of suppressing corrosion due to its chemical properties and improving the fluidity of the molten brazing filler metal.
しかしながら、ケイ素の含有量が0,3wt、%未満、
または、銅の含有量が2wt、%未満では、上述した作
用に所望の効果が得られない、一方、ケイ素の含有量が
5wt、%を超えても、より以上の効果は得られず、逆
に、ろう材の加工性が劣化する問題が生ずる。また、銅
の含有量がLout、%を超えると。However, if the silicon content is less than 0.3wt%,
Alternatively, if the copper content is less than 2 wt.%, the desired effects described above cannot be obtained, while even if the silicon content exceeds 5 wt.%, no further effect can be obtained; Another problem arises in that the workability of the brazing filler metal deteriorates. Moreover, when the copper content exceeds Lout,%.
ろう材の融点が上昇する問題が生ずる。A problem arises in that the melting point of the brazing filler metal increases.
従って、ケイ素の含有量は、0.3から5wt、%の範
囲内に、そして、銅の含有量は、2から10wt、%の
範囲内に限定すべきである。Therefore, the silicon content should be limited to within the range of 0.3 to 5 wt.%, and the copper content within the range of 2 to 10 wt.%.
(3)ケイ素含有量のアルミニウム含有量に対する比
ケイ素含有量のアルミニウム含有量に対する比即ちSi
/A円は、融解したろう材の流動性に影響を及ぼす、従
って、この発明においては、Si/AQ比を0.05か
ら0.12の範囲内にすることが望ましい、Si/AJ
比が0.05未満では、融解したろう材の流動性を十分
に向上させることができない、一方、Si/AΩ比が0
.12を超えると、逆に、融解したろう材の流動性が低
下する。(3) Ratio of silicon content to aluminum content Ratio of silicon content to aluminum content, that is, Si
/A circle affects the fluidity of the melted brazing filler metal. Therefore, in this invention, it is desirable to keep the Si/AQ ratio within the range of 0.05 to 0.12.
If the ratio is less than 0.05, the fluidity of the melted brazing filler metal cannot be sufficiently improved; on the other hand, if the Si/AΩ ratio is 0.
.. If it exceeds 12, on the contrary, the fluidity of the melted brazing filler metal decreases.
この発明のろう材を使用して行なうろう付けは、次のよ
うにして行なわれる。即ち、接合されるべきアルミニウ
ム部材相互を、適当な治具を用いて組み付ける。次いで
、この発明のろう材を、線状または粉末状となし、接合
部に供給する。または、この発明のろう材を、溶射のプ
レコート材またはプレージングシートとして、これらと
アルミニウム部材とを組み付ける0組み付けられたアル
ミニウム部材の接合部にフラックスを塗布する。このよ
うにして組付けられた組立て体を、不活性ガス雰囲気ま
たは大気下の炉内において、400〜500℃の温度で
加熱して、ろう材を溶融させる。かくして、接合部は、
溶融したろう材によって接合される。Brazing using the brazing material of the present invention is performed as follows. That is, the aluminum members to be joined are assembled using a suitable jig. Next, the brazing material of the present invention is formed into a wire or powder and is supplied to the joint. Alternatively, the brazing filler metal of the present invention may be used as a thermal spray precoat material or a plating sheet, and flux may be applied to the joint portion of the assembled aluminum member where the brazing material and the aluminum member are assembled. The thus assembled assembly is heated in a furnace under an inert gas atmosphere or air at a temperature of 400 to 500°C to melt the brazing filler metal. Thus, the joint is
Joined using molten brazing filler metal.
次に、この発明のろう材を、実施例により、この発明の
範囲外のろう材と対比しながら説明する。Next, the brazing filler metal of the present invention will be explained with reference to examples while comparing it with brazing filler metals that are outside the scope of the present invention.
第1表に示すように、この発明の範囲内の化学成分組成
を有する、この発明のろう材の供試体(以下、「本発明
供試体」という)Nclから9と、そして、少なくとも
その成分の1つがこの発明の範囲外の化学成分組成を有
する、比較のためのろう材の供試体(以下、「比較用供
試体」という)!!11から10とを、次に述べる方法
によって調製した6本発明供試体および比較用供試体を
調製するための、第1表に示す化学成分組成を有する円
柱状の鋳塊を1通常の溶解鋳造法によって鋳造した。鋳
造された鋳塊の各々を、所定温度に加熱し、加熱された
鋳塊の各々に対し、熱間押出し加工および温間伸線加工
を施して、直径2mの線状の本発明供試体&1から・8
および比較用供試体N11lから10を調製した0本発
明供試体&9は、第1表に示す化学成分組成を有する鋳
塊を圧延して薄板となし、この薄板を、 JIS 30
03材の上面にろう材として張り合わせ、プレージング
シートとした。As shown in Table 1, specimens of the brazing filler metal of the present invention (hereinafter referred to as "specimens of the present invention") having chemical component compositions within the scope of the present invention, and at least Ncl to 9 of the components. One is a brazing filler metal specimen for comparison (hereinafter referred to as a "comparative specimen"), one of which has a chemical composition outside the scope of this invention! ! 6 cylindrical ingots having the chemical composition shown in Table 1 were prepared by the method described below. It was cast according to the law. Each of the cast ingots was heated to a predetermined temperature, and each of the heated ingots was subjected to hot extrusion and warm wire drawing to form a linear specimen of the present invention with a diameter of 2 m &1. Kara・8
and Comparison specimen N111 to 10 were prepared. The present invention specimen &9 was made by rolling an ingot having the chemical composition shown in Table 1 into a thin plate, and this thin plate was made according to JIS 30.
This was pasted onto the top surface of the 03 material as a brazing material to form a plating sheet.
第1表に、上述した各供試体の融点、ろう材の形態およ
び加工性を併せて示す。Table 1 also shows the melting point, shape of the brazing filler metal, and workability of each of the above-mentioned specimens.
次いで、上述した各供試体の各々を使用してろう付けを
行なったときのろう付け性を、以下に述べる方法によっ
て調べた。即ち、添付図面に示すように、JIS 30
03材の、長さ(a):60m、輻:(b):40−の
平板状アルミニウム部材1の上面に、同じ< JIS
3003材の、長さ(c):50m、高さ(d) :
25■の平板状アルミニウム部材2を、その一端部に配
置した直径1■のSUS製の丸棒状スペーサ3を介して
、垂直に仮りに組付けて組立て体4を形成した。Next, the brazing properties of each of the above-mentioned specimens were examined by the method described below. That is, as shown in the attached drawing, JIS 30
The same < JIS
Length (c): 50m, height (d) of 3003 material:
An assembly 4 was formed by vertically temporarily assembling 25 square aluminum plate-shaped aluminum members 2 through a SUS round bar spacer 3 having a diameter of 1 square placed at one end thereof.
次いで、組立て体4の、平板状アルミニウム部材1と平
板状アルミニウム部材2との接合部に、本発明供試体N
QI〜8および比較用供試体Ncl〜10からなるろう
材5を、それぞれ配置した。Next, the specimen N of the present invention was applied to the joint between the flat aluminum member 1 and the flat aluminum member 2 of the assembly 4.
Brazing filler metals 5 consisting of QI~8 and comparative specimen Ncl~10 were placed, respectively.
また、平板状アルミニウム部材1の代りに、プレージン
グシートからなる本発明供試体&9を使用し、この上面
に平板状アルミニウム部材2を垂直に組付けて組立て体
4を形成した。In addition, instead of the flat aluminum member 1, a specimen &9 of the present invention made of a plating sheet was used, and the flat aluminum member 2 was vertically assembled on the upper surface of this specimen to form an assembly 4.
次いで、上述した組立て体4に、KCI −LiC1系
フラックスを塗布し、加熱炉内において、大気下で、ろ
う材の融点よりも30〜50℃高い温度に加熱して、ろ
う材を融解し、かくして、融解したろう材によって、組
立て体4の接合部をろう付けした。Next, a KCI-LiC1-based flux is applied to the above-described assembly 4, and heated in the atmosphere in a heating furnace to a temperature 30 to 50° C. higher than the melting point of the brazing material to melt the brazing material, Thus, the joints of the assembly 4 were brazed with the molten brazing filler metal.
このようにしてろう付けしたときの、各供試体のろう材
の流動長、ろう材によるアルミニウム部材1,2への侵
食深さ、および、ろう材の酸化皮膜の厚さを測定し、ろ
う付け温度とともに、第1表に併せて示した。When brazed in this way, the flow length of the brazing filler metal of each specimen, the depth of erosion of the aluminum members 1 and 2 by the brazing filler metal, and the thickness of the oxide film of the brazing filler metal were measured. It is also shown in Table 1 along with the temperature.
第1表から明らかなように、 Zn:99wt、%の比
較用供試体&1を使用してろう付けしたときは、アルミ
ニウム部材への侵食が大であった。 Zn:94wt、
%、残り:AΩの比較用供試体&2を使用してろう付け
したときは、酸化皮膜が厚くろう付け性が悪かったa
Z n : 59 wt−%、残り:AQの比較用供
試体&3を使用してろう付けしたときは、酸化皮膜が厚
くろう付け性が悪い上、ろう材の加工性も不良であった
。Si:10wt.%、残り:AΩの比較用供試体&4
を使用してろう付けしたときは、ろう付け温度が高く、
アルミニウム部材が、溶融または変形した。As is clear from Table 1, when the comparison specimen &1 containing Zn: 99wt% was used for brazing, the corrosion of the aluminum member was large. Zn: 94wt,
%, remaining: When brazing was performed using AΩ comparison specimen &2, the oxide film was thick and the brazing performance was poor a
When brazing was performed using comparative specimen &3 with Zn: 59 wt-% and remainder: AQ, the oxide film was thick and the brazing properties were poor, and the processability of the brazing material was also poor. Si: 10wt. %, remaining: AΩ comparative specimen &4
When brazing using
The aluminum member melted or deformed.
亜鉛の含有量が本発明の範囲を外れて少ない比較用供試
体N115を使用してろう付けしたときは、ろう付け温
度が高く、アルミニウム部材が溶融または変形した。亜
鉛の含有量が本発明の範囲を外れて多い比較用供試体&
6を使用してろう付けしたときは、アルミニウム部材の
侵食が大であった。When brazing was performed using comparative specimen N115 whose zinc content was outside the range of the present invention, the brazing temperature was high and the aluminum member melted or deformed. Comparative specimens with high zinc content outside the range of the present invention &
When brazing was performed using No. 6, corrosion of the aluminum member was significant.
ケイ素の含有量が本発明の範囲を外れて少ない比較用供
試体&7.および、銅の含有量が本発明の範囲を外れて
少ない比較用供試体&9を使用してろう付けしたときは
、酸化皮膜が厚く、ろう付け性が悪く、且つ、融解した
ろう材の流動性が不良であった。Comparative specimen with a low silicon content outside the range of the present invention &7. When brazing was performed using Comparative Specimen &9 with a low copper content outside the range of the present invention, the oxide film was thick, the brazing properties were poor, and the fluidity of the molten brazing filler metal was poor. was defective.
ケイ素の含有量が本発明の範囲を外れて多い比較用供試
体Nn8は、ろう材の加工性が悪かった。Comparative specimen Nn8, in which the silicon content was higher than the range of the present invention, had poor processability of the brazing filler metal.
銅の含有量が本発明の範囲を外れて多い比較用供試体N
n1Oは、融点が高過ぎるので、ろう付け性試験を行な
うことができなかった。Comparative specimen N whose copper content is higher than the range of the present invention
Since the melting point of n1O was too high, it was not possible to conduct a brazeability test.
これに対して、本発明供試体Nα1から9の各々を使用
してろう付けしたときは、何れも、ろう付け温度が低く
、従って、アルミニウム部材が、溶融または変形するこ
とがなく、融解したろう材の流動性も良好であり、アル
ミニウム部材への侵食は少なく、そして、酸化皮膜は薄
くて、ろう付け性が良好であった。On the other hand, when each of the present invention specimens Nα1 to Nα9 was used for brazing, the brazing temperature was low, so the aluminum member did not melt or deform, and the melted wax The fluidity of the material was good, there was little corrosion to the aluminum member, and the oxide film was thin, giving good brazing properties.
以上述べたように、この発明のろう材によれば、低融点
のアルミニウム部材を、溶融や変形が生ずることなく、
そして、能率的にろう付けすることができ、しかも、品
質の優れた接合部が得られる、工業上有用な効果がもた
らされる。As described above, according to the brazing material of the present invention, aluminum members having a low melting point can be heated without melting or deforming.
This provides an industrially useful effect in that brazing can be performed efficiently and a joint of excellent quality can be obtained.
図面は、ろう付け試験用アルミニウム部材の組立て体を
示す斜視図である。図面において、1.2・・・アルミ
ニウム部材、3・・・スペーサ、4・・・組立て体、
5・・・ろう材。
出願人 三菱アルミニウム株式会社
代理人 潮 谷 京 津 夫The drawing is a perspective view showing an assembly of aluminum members for brazing test. In the drawings, 1.2...aluminum member, 3...spacer, 4...assembly,
5... Brazing material. Applicant Mitsubishi Aluminum Co., Ltd. Agent Kyo Tsuo Shioya
Claims (4)
け用ろう材。1. Zinc: 85-97wt. %, silicon: 0.3-5wt. A brazing filler metal for brazing aluminum parts, the brazing filler metal comprising: % and the remainder: aluminum and unavoidable impurities.
け用ろう材。2. Zinc: 85-97wt. %, copper: 2-10wt. %, and the remainder consists of aluminum and unavoidable impurities.
け用ろう材。3. Zinc: 85-97wt. %, silicon: 0.3-5wt. %, copper: 2-10wt. %, and the remainder consists of aluminum and unavoidable impurities.
アルミニウムの含有量に対する比は、0.05から0.
12の範囲内である、請求項1または3記載のろう材。4. The ratio of the silicon content to the aluminum content in the brazing filler metal is between 0.05 and 0.05.
The brazing material according to claim 1 or 3, which is within the range of 12.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2156121A JP3020998B2 (en) | 1990-06-14 | 1990-06-14 | Brazing material for brazing aluminum members |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2156121A JP3020998B2 (en) | 1990-06-14 | 1990-06-14 | Brazing material for brazing aluminum members |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPH0446695A true JPH0446695A (en) | 1992-02-17 |
| JP3020998B2 JP3020998B2 (en) | 2000-03-15 |
Family
ID=15620781
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2156121A Expired - Fee Related JP3020998B2 (en) | 1990-06-14 | 1990-06-14 | Brazing material for brazing aluminum members |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JP3020998B2 (en) |
Cited By (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2012006071A (en) * | 2010-06-28 | 2012-01-12 | Nanojoin Kk | Zinc alloy and end face electrode material for metallized plastic film capacitor |
| JP2012180557A (en) * | 2011-03-01 | 2012-09-20 | Kobe Steel Ltd | Zinc alloy cast ingot having excellent workability and method for producing the zinc alloy cast ingot |
| JP2012179632A (en) * | 2011-03-01 | 2012-09-20 | Kobe Steel Ltd | Zn-Al-Cu ALLOY ROLLED MATERIAL AND METHOD FOR PRODUCING THE SAME |
| EP2478992A3 (en) * | 2008-04-21 | 2012-11-07 | Honda Motor Co., Ltd. | Method for joining metallic members and brazing filler metal |
| JP2012228729A (en) * | 2011-04-27 | 2012-11-22 | Sumitomo Metal Mining Co Ltd | Pb FREE SOLDER ALLOY MAKING Zn PRINCIPAL INGREDIENT AND METHOD OF MANUFACTURING THE SAME |
| WO2014021308A1 (en) * | 2012-07-31 | 2014-02-06 | 株式会社テリーサ研究所 | Solder alloy for bonding metal, and soldering method using same |
| US20160053347A1 (en) * | 2013-04-12 | 2016-02-25 | Homda Motor Co., Ltd. | Method for producing zinc alloy |
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1990
- 1990-06-14 JP JP2156121A patent/JP3020998B2/en not_active Expired - Fee Related
Cited By (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP2478992A3 (en) * | 2008-04-21 | 2012-11-07 | Honda Motor Co., Ltd. | Method for joining metallic members and brazing filler metal |
| EP2614916A1 (en) * | 2008-04-21 | 2013-07-17 | Honda Motor Co., Ltd. | Method for joining metallic members and brazing filler metal |
| JP2012006071A (en) * | 2010-06-28 | 2012-01-12 | Nanojoin Kk | Zinc alloy and end face electrode material for metallized plastic film capacitor |
| JP2012180557A (en) * | 2011-03-01 | 2012-09-20 | Kobe Steel Ltd | Zinc alloy cast ingot having excellent workability and method for producing the zinc alloy cast ingot |
| JP2012179632A (en) * | 2011-03-01 | 2012-09-20 | Kobe Steel Ltd | Zn-Al-Cu ALLOY ROLLED MATERIAL AND METHOD FOR PRODUCING THE SAME |
| JP2012228729A (en) * | 2011-04-27 | 2012-11-22 | Sumitomo Metal Mining Co Ltd | Pb FREE SOLDER ALLOY MAKING Zn PRINCIPAL INGREDIENT AND METHOD OF MANUFACTURING THE SAME |
| WO2014021308A1 (en) * | 2012-07-31 | 2014-02-06 | 株式会社テリーサ研究所 | Solder alloy for bonding metal, and soldering method using same |
| JP5937214B2 (en) * | 2012-07-31 | 2016-06-22 | 株式会社テリーサ研究所 | Solder alloy for metal bonding and soldering method using the same |
| US20160053347A1 (en) * | 2013-04-12 | 2016-02-25 | Homda Motor Co., Ltd. | Method for producing zinc alloy |
| US9376737B2 (en) * | 2013-04-12 | 2016-06-28 | Honda Motor Co., Ltd. | Method for producing zinc alloy |
| EP2985355A4 (en) * | 2013-04-12 | 2016-12-07 | Honda Motor Co Ltd | Method for producing zinc alloy |
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| Publication number | Publication date |
|---|---|
| JP3020998B2 (en) | 2000-03-15 |
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