JPH0390274A - Vapor brazing method for al or al alloy - Google Patents

Vapor brazing method for al or al alloy

Info

Publication number
JPH0390274A
JPH0390274A JP22117389A JP22117389A JPH0390274A JP H0390274 A JPH0390274 A JP H0390274A JP 22117389 A JP22117389 A JP 22117389A JP 22117389 A JP22117389 A JP 22117389A JP H0390274 A JPH0390274 A JP H0390274A
Authority
JP
Japan
Prior art keywords
brazing
alloy
flux
brazed
zncl2
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.)
Pending
Application number
JP22117389A
Other languages
Japanese (ja)
Inventor
Motoyoshi Yamaguchi
山口 元由
Hitoshi Koyama
小山 斉
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.)
Furukawa Aluminum Co Ltd
Original Assignee
Furukawa Aluminum Co Ltd
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 Furukawa Aluminum Co Ltd filed Critical Furukawa Aluminum Co Ltd
Priority to JP22117389A priority Critical patent/JPH0390274A/en
Publication of JPH0390274A publication Critical patent/JPH0390274A/en
Pending legal-status Critical Current

Links

Abstract

PURPOSE:To shorten the production process for the heat exchanger of automobiles, etc., by brazing Al members in a nonoxidative atmosphere where the vapor emitted from the reaction melt of ZnCl2 and Al exists. CONSTITUTION:A rolled plate 2 of Al or Al alloy is brazed to a brazing sheet 1 formed by using Al or Al alloy as a core material and cladding a Al brazing material thereto. The two sheets 1, 2 are brazed in the nonoxidative atmosphere where the vapor emitted from the reaction melt of the ZnCl2 and Al exists. The brazing is executed by heating for 5 minutes at 610 deg.C in an electric furnace contg. a mixture composed of 200g ZnCl2 and 200g Al powder per 1m<3> inside volume of the brazing furnace. The improved quality, such as improved corrosion resistance, is obtd. in this way.

Description

【発明の詳細な説明】 〔産業上の利用分野〕 本発明は、Al又はAl合金のろう付方法に関するもの
であり、例えば自動車の熱交換器の製造においてそのろ
う付された部材の性能を向上させるとともに製造コスト
を安価にするものである。
DETAILED DESCRIPTION OF THE INVENTION [Field of Industrial Application] The present invention relates to a method for brazing Al or Al alloy, and is used to improve the performance of brazed members, for example, in the manufacture of heat exchangers for automobiles. This also reduces the manufacturing cost.

〔従来の技術〕[Conventional technology]

通常AlまたはAl合金のろう付は、接合しようとする
AlまたはAl合金部材を、これらAl等よりも融点の
低いろう材を介して固定して組立物とし、このろう材の
融点よりも高く、接合しようとするAlまたはAl合金
部材の融点よりも低い温度に加熱することにより行なっ
ている。そしてろう材としては一般にAl−3i系合金
が使用され、その形状としては板状。
Normally, in brazing Al or Al alloy, the Al or Al alloy members to be joined are fixed together via a brazing filler metal whose melting point is lower than that of Al, etc., and the melting point is higher than that of the brazing filler metal. This is done by heating to a temperature lower than the melting point of the Al or Al alloy members to be joined. Generally, Al-3i alloy is used as the brazing material, and its shape is a plate.

線状、粉末状としたろう材あるいはAlまたはA4合金
からなる芯材にこのろう材を被覆した合わせ材(以下プ
レージングシートと記す)として用いられている。
It is used as a laminated material (hereinafter referred to as a plating sheet) in which a wire or powdered brazing material or a core material made of Al or A4 alloy is coated with this brazing material.

従来のろう付方法としては、ろう付をする部材表面の酸
化被膜を除去するためのフラックスを用いるフラックス
ろう付性と、これを用いない真空ろう付性が通常使用さ
れている。上記フラックスろう付性としては、組立物に
塩化物系フラックスを塗布してろう付加熱する炉中ろう
付性等がある。ところがこの塩化物系フラックスは、A
lに対しては腐食性であるのでろう付換洗浄して完全に
除去しなければならず、製造工程が非常に煩雑である。
As conventional brazing methods, flux brazing, which uses flux to remove an oxide film on the surfaces of parts to be brazed, and vacuum brazing, which does not use flux, are commonly used. The above-mentioned flux brazing properties include furnace brazing properties in which a chloride-based flux is applied to the assembly and heated for brazing. However, this chloride-based flux is
Since it is corrosive to L, it must be completely removed by cleaning after brazing, making the manufacturing process very complicated.

これに対し、真空中に接合しようとする組立物を置いて
ろう付加熱する真空ろう付性によれば、後工程として洗
浄も不要であり、またろう付後の部材表面も良好である
が、高真空が必要であることおよび材料的に制約がある
等の問題がある。
On the other hand, vacuum brazing, in which the assembly to be joined is placed in a vacuum and subjected to brazing and heating, does not require cleaning as a post-process, and the surface of the parts after brazing is also good. There are problems such as the need for high vacuum and material limitations.

更に、最近上記不具合を解消するろう付性として、弗化
物系フラックスを用いて炉中でろう付する方法が広く用
いられるようになってきた。
Furthermore, recently, a method of brazing in a furnace using a fluoride flux has been widely used as a method of brazing to solve the above-mentioned problems.

この方法は特公昭58−27037号公報に記載されて
いるようにフラックスとして非吸湿性でlに対して非腐
食性のKAlF4とに、At F6の混合物を用い、こ
れを水に懸濁させ、接合しようとする組立物表面に塗布
してろう付するものであり、その特徴としては非腐食性
フラックスを用いるためにフラックス除去の後処理が不
要なことが上げられる。
As described in Japanese Patent Publication No. 58-27037, this method uses a mixture of AtF6 and KAlF4, which is non-hygroscopic and non-corrosive to l, as a flux, and suspends this in water. It is applied to the surfaces of the assemblies to be joined and brazed, and its feature is that since it uses non-corrosive flux, no post-treatment to remove the flux is required.

〔発明が解決しようとする課題〕[Problem to be solved by the invention]

しかしながら上記特公昭58−27037号公報に記載
の方法においては、必然的にフラックスを組立物表面に
付着させるための塗布、乾燥工程が必要であり、さらに
塗布されてフラックスはその組立物を次工程へ運ぶ途中
で組立物から脱落するものが多く、このため有効に使用
されるフラックスの掛止りは低くなる。またろう付後の
接合部材の表面には不均一にフラックス残渣が残るので
、従来の真空ろう付性に比較して表面が汚れ商品価値が
劣ると共に、耐食性を向上させるために次工程で行うク
ロメート処理や黒色塗装処理等が不均一となってしまい
、その効果が十分に発揮されなくなる等の欠点があった
However, the method described in Japanese Patent Publication No. 58-27037 necessarily requires coating and drying steps to adhere the flux to the surface of the assembly. Many items fall off from the assembly during transport, and therefore the flux that can be used effectively is reduced. Furthermore, since flux residue remains unevenly on the surface of the joined parts after brazing, the surface becomes dirty compared to conventional vacuum brazing, and the commercial value is inferior. There were drawbacks such as the treatment, black coating, etc. becoming non-uniform and the effects not being fully exhibited.

さらにはフラックス残渣は非導電性であるため、例えば
熱交換器において犠牲フィンにより管体を保護する防食
法を採用する場合には、防食電流の流れが阻害されてし
まい防食効果が十分得られない場合がある。
Furthermore, since flux residue is non-conductive, for example, when adopting a corrosion prevention method that protects the pipe body with sacrificial fins in a heat exchanger, the flow of anticorrosion current is obstructed, making it impossible to obtain a sufficient corrosion protection effect. There are cases.

またMg含有Al合金を弗化物系フラックスを用いて炉
中ろう付する場合は、従来に比べてろう付性が劣ってい
るため、工業的に安定したろう付性を得るためにはMg
の含有量は0.6wt%(以下wt%を単に%と略記す
る)未満でなければならない。そしてこれ以上のMgを
含有するAl合金では、フラックス塗布量を多くしても
ろう付は難しくなってしまう。この原因はAl合金中の
Jとフラックス成分の弗素とがろう付加熱中に反応する
ためであり、その結果フラックスの組成が変化してフラ
ックスとしての効果が失われること、Al合金中のMg
が表面層に拡散して表面層のMg濃度が高くなること、
およびフラックスがAl合金の表面層に入り込む等の現
象が発生してろうの流れを阻害すること等が起こるから
である。このようにMg含有量の多いAl合金が熱交換
器用材料として使用できないことは、熱交換器の耐久性
や軽量化の面で大きな障害となっていた。
Furthermore, when brazing Mg-containing Al alloys in a furnace using fluoride flux, the brazing properties are inferior to conventional ones, so in order to obtain industrially stable brazing properties, it is necessary to
The content of must be less than 0.6 wt% (hereinafter wt% is simply abbreviated as %). If the Al alloy contains more Mg than this, brazing becomes difficult even if the amount of flux applied is increased. The cause of this is that J in the Al alloy and fluorine, which is a flux component, react with each other during brazing heat, and as a result, the composition of the flux changes and its effectiveness as a flux is lost.
diffuses into the surface layer, increasing the Mg concentration in the surface layer,
This is because phenomena such as flux entering the surface layer of the Al alloy occur and inhibiting the flow of the solder. The fact that Al alloys with such a high Mg content cannot be used as a material for heat exchangers has been a major obstacle in terms of durability and weight reduction of heat exchangers.

更に例えば第2図に示すコンデンサーを製造する場合に
は耐食性を向上させるために、ろう付前に予め管材(3
)の表面にZnを被覆する工程が必要であり、製造コス
トアップの要因となっている。
Furthermore, when manufacturing the capacitor shown in Fig. 2, for example, in order to improve corrosion resistance, the tube material (3
) is required, which is a factor in increasing manufacturing costs.

〔課題を解決するための手段〕[Means to solve the problem]

本発明は、これに鑑み種々検討の結果、接合しようとす
る組立物に直接フラックスを塗布する工程を必要としな
い気相ろう付性を開発したものでAlまたはAl合金を
ろう材を介してろう付する方法において、Al又はAl
合金部材をZnCl2とAlとの反応溶融物からでる蒸
気が存在する非酸化性雰囲気中でろう付することを特徴
とするものである。
In view of this, as a result of various studies, the present invention has developed vapor phase brazing properties that do not require the process of directly applying flux to the assemblies to be joined. In the method of attaching Al or Al
The method is characterized in that alloy parts are brazed in a non-oxidizing atmosphere in the presence of steam from a reaction melt of ZnCl2 and Al.

〔作 用〕[For production]

ZnC1zとAlとの反応溶融物からでる蒸気が存在す
る非酸化性雰囲気中に、接合しようとする部材としての
組立物をおくことにより、この蒸気は極微量かつ均一に
組立物に付着してその表面のAlの酸化皮膜を破壊する
のでろうの濡れを促進し、ろうが−様に流れ、組立物の
接合箇所に均一なフィレットが形成される特徴を有する
By placing the assembly, which is the member to be joined, in a non-oxidizing atmosphere in which steam from the reaction melt of ZnC1z and Al exists, a very small amount of this vapor will uniformly adhere to the assembly and cause its damage. Since it destroys the Al oxide film on the surface, it promotes wetting of the solder, and has the characteristic that the solder flows in a uniform manner and forms a uniform fillet at the joints of the assembly.

そしてこの蒸気を発生させるにはznC12とAl粉末
とを均一に混合し、あるいはAl製のトレー上にZnC
1,を置き、ろう付を実施する炉中に予め入れておき、
炉を昇温したときにその熱で同時に蒸発させても良いし
、またこの蒸気を炉外で発生させて窒素ガス等をキャリ
アーとして炉内に供給する等の方法も可能である。さら
に非酸化性雰囲気中にこの蒸気を存在させることにより
、組立物は完全に蒸気で覆うことができるので、蒸気密
度は少なくてすみフラックス消費量を低減することがで
きる。なお非酸化性雰囲気としては例えば窒素、アルゴ
ン、−酸化炭素その他いずれの雰囲気でも利用可能であ
る。
To generate this steam, ZnC12 and Al powder are mixed uniformly, or ZnC is placed on an Al tray.
1, placed in advance in the furnace where brazing is to be carried out,
When the temperature of the furnace is raised, the vapor may be simultaneously evaporated using the heat, or it is also possible to generate this steam outside the furnace and supply it into the furnace using nitrogen gas or the like as a carrier. Furthermore, by having this vapor in a non-oxidizing atmosphere, the assembly can be completely covered with vapor, so less vapor density is required and flux consumption is reduced. Note that as the non-oxidizing atmosphere, for example, nitrogen, argon, carbon oxide, or any other atmosphere can be used.

また本発明を実施するには密閉度の高い炉の使用が好ま
しいが、密閉度の劣る炉であっても接合しようとする組
立物をステンレス等からなる容器内にZnCA’2とA
l粉末の混合物と共に入れ、あるいはAl製の容器内に
ZnCl2と共に入れてろう付加熱すれば容易にろう付
することができる。
Furthermore, in order to carry out the present invention, it is preferable to use a highly airtight furnace, but even if a furnace with a poor airtightness is used, the assembly to be joined is placed in a container made of stainless steel or the like and ZnCA'2 and A
It can be easily brazed by placing it together with a mixture of ZnCl2 powder or in an Al container together with ZnCl2 and heating it for brazing.

さらに本発明によれば、Mgを0.6%を超えて含有す
るAl −Mg系合金であってもろう付が可能となる。
Furthermore, according to the present invention, even Al-Mg alloys containing more than 0.6% of Mg can be brazed.

これはZnCA’zの溶融物から出る蒸気と合金中のM
gとが反応しないためである。
This is due to the steam coming out of the ZnCA'z melt and the M in the alloy.
This is because it does not react with g.

更に蒸気中のZnはろう何時にろう付物表面に拡散し、
Zn濃度2%、深さ5(l1m程度のZn拡散層を形成
する。この層が未拡散層に対して電位的に卑であるので
未拡散層を保護し貫通孔食を防止するために耐食性が向
上する。従ってろう付の前工程でのZn被覆処理が不用
となる。
Furthermore, Zn in the steam diffuses onto the surface of the brazing object during the soldering process,
A Zn diffusion layer with a Zn concentration of 2% and a depth of about 5 (11 m) is formed. Since this layer has a lower potential than the undiffused layer, it is made with corrosion resistance to protect the undiffused layer and prevent through-hole corrosion. Therefore, Zn coating treatment in the pre-brazing process becomes unnecessary.

〔実施例〕〔Example〕

以下本発明を実施例について説明する。 The present invention will be described below with reference to Examples.

実施例1 第1図に示す逆T継手試験片を組立て本発明法によりろ
う付接合した。即ちIts^3003 CAl−Cu 
O,05〜0.20%−Mnt、[l〜l、5%)合金
を芯材とし、この片面にSi6,8〜8.2%を含むJ
IS 4343Al合金ろう材をクラッドしたItsB
^12PCのプレージングシート(1)からなる厚さ1
mnc7)圧延板トIts Al050. JIS A
3003. Al −0゜8%Mgの厚さ1開の圧延板
(2)とを組立て有機溶剤により脱脂した。
Example 1 The inverted T-joint test piece shown in FIG. 1 was assembled and brazed together by the method of the present invention. That is, Its^3003 CAl-Cu
J containing O,05~0.20%-Mnt,[l~l,5%) alloy as a core material and containing Si6,8~8.2% on one side.
ItsB clad with IS 4343 Al alloy brazing filler metal
^Thickness 1 consisting of 12pcs plating sheet (1)
mnc7) Rolled plate Its Al050. JIS A
3003. A 1-thick rolled plate (2) of Al-0°8%Mg was assembled and degreased with an organic solvent.

そして組立物をろう付炉の内容積1ボ当たり200gの
ZnCl2と200HのAl粉末との混合物を載置した
ステンレス製のトレー上に組立物を置き、露点−40℃
、酸素濃度1[lllppmの窒素ガス雰囲気で置換さ
れ、610℃に保持された電気炉内にこの組立物を挿入
し、組立物を610℃で5分間加熱してろう付を実施し
た。
Then, the assembly was placed on a stainless steel tray containing a mixture of 200 g of ZnCl2 and 200H Al powder per inner volume of the brazing furnace, and the dew point was -40°C.
This assembly was inserted into an electric furnace that was purged with a nitrogen gas atmosphere with an oxygen concentration of 1 ppm and maintained at 610°C, and was heated at 610°C for 5 minutes to perform brazing.

上記ろう付換の接合物を炉外に取り出しろう付状況を調
べ、ろう付状況が良好な物を○、不良なものを×として
これらの結果を第1表に示した。
The re-brazed joints were taken out of the furnace and their brazing conditions were examined, and the results are shown in Table 1, with good brazing conditions marked as ○ and poor brazing conditions marked as x.

また従来法として、上記脱脂後の組立物に10%濃度の
KA、gF4を塗布し乾燥後、露点−40℃、酸素濃度
1100ppの窒素ガス雰囲気で置換され、610℃に
保持された電気炉内にこの組立物を挿入し、組立物を6
10℃で5分間加熱してろう付を実施した。この結果を
まとめて第1表に示した。
In addition, as a conventional method, 10% concentration of KA and gF4 is applied to the above degreased assembly, and after drying, the air is replaced with a nitrogen gas atmosphere with a dew point of -40°C and an oxygen concentration of 1100pp, and the temperature is maintained at 610°C. Insert this assembly into the
Brazing was performed by heating at 10° C. for 5 minutes. The results are summarized in Table 1.

第1表より明らかなように、本発明例NO,l〜N0.
3では何れもろう付性は良好であり、特にMg含有材で
も良好なろう付が出来た。これに対し従来例No、6の
AJ−0,8%Mg材ではろう付は出来なかった。
As is clear from Table 1, invention examples No. 1 to No. 0.
In No. 3, the brazing properties were good in all cases, and particularly good brazing was achieved even with the Mg-containing material. On the other hand, brazing was not possible with the AJ-0.8% Mg material of Conventional Example No. 6.

実施例2 第2図に示すように、常法により管状に熱間押出し成形
したAl−0,5%Cu合金の管材(3)を蛇行状に曲
げ、この蛇行状管材(3)の間にJISA3003 C
Al−1%Mg)を芯材とし、その両面にJIS^43
43 CAl−7%Si)皮材を各々10%の割合でク
ラッドした厚さ0.Ibmのプレージングシートからな
るコルゲートフィン(4)を挟み、さらにAl−4,3
%Zn−1,3%Mg合金からなるコネクター(5)を
AlO?0の溶接棒を用いてTIG溶接し、サーペンタ
インタイプのコンデンサーを組立て有機溶剤で脱脂した
Example 2 As shown in Fig. 2, an Al-0.5% Cu alloy tube (3) hot-extruded into a tubular shape by a conventional method is bent into a serpentine shape, and between the serpentine tubes (3) JISA3003C
Al-1%Mg) as the core material, and JIS^43 on both sides.
43 CAl-7%Si) cladding material at a ratio of 10% to a thickness of 0. A corrugated fin (4) made of IBM plating sheet is sandwiched, and Al-4,3
%Zn-1.3%Mg alloy connector (5) with AlO? A serpentine type capacitor was assembled by TIG welding using a No. 0 welding rod and degreased with an organic solvent.

そしてこの組立物をろう付炉の内容積lTl1当たり 
350gのZnCl2を載置したAl製のトレー上に組
立物を置き、露点−40℃、酸素濃度10tlppmの
窒素ガス雰囲気で置換され、610℃に保持された電気
炉内にこの組立物を挿入し、組立物を610℃で5分間
加熱してろう付を実施、し、炉外へ取り出して冷却後微
量のCIを除去するために80℃で1分間湯洗し、乾燥
した。
Then, this assembly is
The assembly was placed on an Al tray on which 350 g of ZnCl2 was placed, and the assembly was inserted into an electric furnace maintained at 610 °C and purged with a nitrogen gas atmosphere with a dew point of -40 °C and an oxygen concentration of 10 tlppm. The assembly was heated at 610° C. for 5 minutes to perform brazing, taken out from the furnace, cooled, and then washed with hot water at 80° C. for 1 minute to remove traces of CI, and then dried.

上記ろう付換のコンデンサー表面の外観観察を行い、ま
たろう付状況を調べてこれらの結果を第2表に示した。
The appearance of the surface of the capacitor after brazing was observed, and the brazing condition was examined. The results are shown in Table 2.

その後常法によりクロメート処理、黒色塗装を行いこれ
らの付着性をクロメート性、塗装性として第2表に示し
た。
Thereafter, chromate treatment and black coating were carried out using conventional methods, and the adhesion properties thereof are shown in Table 2 as chromate properties and paint properties.

またこの塗装後のコンデンサーの耐食性を評価するため
、11588681に基づ<CASS試験を500時間
実施し、貫通孔食の有無を調べその結果を第2表に併記
した。
Furthermore, in order to evaluate the corrosion resistance of the capacitor after coating, a <CASS test was conducted for 500 hours based on 11588681, and the presence or absence of through pitting corrosion was examined and the results are also listed in Table 2.

従来例として比較のため上記第2図に示すコンデンサー
の組立物を従来法でろう付したものについて、その特性
を調査した。
As a conventional example, for comparison, the characteristics of the capacitor assembly shown in FIG. 2, which was brazed using a conventional method, were investigated.

即ち第2図に示す組立物を有機溶剤により脱脂したのち
、10%濃度のKAlFa懸濁液を塗布し200℃で1
0分間の乾燥を行った。その後露点−40℃、酸素濃度
1100ppの窒素ガス雰囲気で置換され、610℃に
保持された電気炉内にこの組立物を挿入してfilFで
5分間加熱してろう付を行った。
That is, after degreasing the assembly shown in Fig. 2 with an organic solvent, a 10% concentration KAlFa suspension was applied and the mixture was heated at 200°C.
Drying was performed for 0 minutes. Thereafter, this assembly was inserted into an electric furnace maintained at 610°C and purged with a nitrogen gas atmosphere with a dew point of -40°C and an oxygen concentration of 1100pp, and brazed by heating with filF for 5 minutes.

その後の工程は上記本発明例と同様に行い、かつこのろ
う付されたコンデンサーについて上記と同様な評価試験
を行ってそれらの結果について第2表に示した。
The subsequent steps were carried out in the same manner as in the above-mentioned examples of the present invention, and the brazed capacitors were subjected to the same evaluation tests as above, and the results are shown in Table 2.

第2表 注1) 注2) 接合率(%) =((フィン全山数−未接合山数)/フィンの全山数)
 X 1tlf)フィレット長さ(mm)は第3図に示
す管材(3)とフィン(4)のAで示す接合長さをいう
Table 2 Note 1) Note 2) Bonding rate (%) = ((Total number of fin ridges - Number of unbonded ridges)/Total number of fin ridges)
X 1tlf) Fillet length (mm) refers to the joining length shown by A between the tube material (3) and the fin (4) shown in FIG.

第2表より明らかなように本発明によるろう付換のコン
デンサーの表面はきれいであり、ろう付状況も良好であ
った。さらにクロメート性、塗装性も良好で、耐食性も
良好であった。
As is clear from Table 2, the surface of the re-brazed capacitor according to the present invention was clean and the brazing condition was good. Furthermore, the chromate property and paintability were also good, and the corrosion resistance was also good.

これに対し従来法によるコンデンサーは表面にフラッグ
ス残渣が全面に濃く不均一に付着しており、外観上好ま
しくない。またろう付状況は良好であったが、ろう付換
のクロメート処理および塗装は不均一であり、耐食性に
ついては管材で貫通孔食が発生した。
On the other hand, in the capacitor manufactured by the conventional method, the flag residue is thickly and non-uniformly adhered to the entire surface of the capacitor, which is unfavorable in terms of appearance. Furthermore, although the brazing condition was good, the chromate treatment and painting for brazing replacement were uneven, and as for corrosion resistance, through-pitting corrosion occurred in the pipe material.

[発明の効果] このように本発明によれば、従来のろう付性に比べて例
えば自動車等の熱交換器の製造工程が短縮できるので製
造コストが安価になり、またろう付換の表面がきれいで
あるためクロメート処理等の後処理での表面処理性が良
好で耐食性に優れる等の品質が向上し、さらにMgを多
く含有する合金のろう付も可能である等工業上顕著な効
果を奏するものである。
[Effects of the Invention] As described above, according to the present invention, the manufacturing process for heat exchangers for automobiles, etc., can be shortened compared to conventional brazing properties, resulting in lower manufacturing costs, and the surface of re-brazing can be reduced. Because it is clean, it has good surface treatment properties in post-treatments such as chromate treatment, improves quality such as excellent corrosion resistance, and has remarkable industrial effects such as being able to braze alloys containing a large amount of Mg. It is something.

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

第1図は逆T継手試験片を示す斜視図、第2図はエアコ
ン用熱交換器であるサーペンタイプコンデンサーの一例
を示す斜視図、第3図は第2図の管とフィンの接合部を
拡大して示す側面図である。 l・・・プレージングシ一ト 2・・・Al合金 3・・・管材 4・・・フィン 5・・・コネクター 第1図 第2図 第3図 L−a −J
Figure 1 is a perspective view of an inverted T-joint test piece, Figure 2 is a perspective view of an example of a serpentine condenser, which is a heat exchanger for air conditioners, and Figure 3 shows the joint between the tube and fin in Figure 2. It is an enlarged side view. l... Placing seat 2... Al alloy 3... Tube material 4... Fin 5... Connector Fig. 1 Fig. 2 Fig. 3 Fig. L-a -J

Claims (1)

【特許請求の範囲】[Claims] (1)Al又はAl合金をAl合金系ろう材を介してろ
う付する方法において、Al又はAl合金部材をZnC
l_2とAlとの反応溶融物からでる蒸気が存在する非
酸化性雰囲気中でろう付することを特徴とするAl又は
Al合金の気相ろう付方法。
(1) In a method of brazing Al or Al alloy through an Al alloy brazing material, the Al or Al alloy member is
1. A vapor phase brazing method for Al or Al alloy, characterized in that brazing is carried out in a non-oxidizing atmosphere in the presence of steam from a reaction melt of l_2 and Al.
JP22117389A 1989-08-28 1989-08-28 Vapor brazing method for al or al alloy Pending JPH0390274A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP22117389A JPH0390274A (en) 1989-08-28 1989-08-28 Vapor brazing method for al or al alloy

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP22117389A JPH0390274A (en) 1989-08-28 1989-08-28 Vapor brazing method for al or al alloy

Publications (1)

Publication Number Publication Date
JPH0390274A true JPH0390274A (en) 1991-04-16

Family

ID=16762621

Family Applications (1)

Application Number Title Priority Date Filing Date
JP22117389A Pending JPH0390274A (en) 1989-08-28 1989-08-28 Vapor brazing method for al or al alloy

Country Status (1)

Country Link
JP (1) JPH0390274A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4870074A (en) * 1986-04-30 1989-09-26 Dainippon Pharmaceutical Co., Ltd. Substituted benzamide derivatives, for enhancing gastrointestinal motility

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4870074A (en) * 1986-04-30 1989-09-26 Dainippon Pharmaceutical Co., Ltd. Substituted benzamide derivatives, for enhancing gastrointestinal motility

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