JPS5825452A - Al alloy for fin material of heat exchanger with superior dropping resistance and sacrificial anode effect - Google Patents

Al alloy for fin material of heat exchanger with superior dropping resistance and sacrificial anode effect

Info

Publication number
JPS5825452A
JPS5825452A JP12272081A JP12272081A JPS5825452A JP S5825452 A JPS5825452 A JP S5825452A JP 12272081 A JP12272081 A JP 12272081A JP 12272081 A JP12272081 A JP 12272081A JP S5825452 A JPS5825452 A JP S5825452A
Authority
JP
Japan
Prior art keywords
alloy
heat exchanger
brazing
superior
fin
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
JP12272081A
Other languages
Japanese (ja)
Other versions
JPH028018B2 (en
Inventor
Ken Toma
当摩 建
Isao Takeuchi
竹内 庸
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.)
MA Aluminum Corp
Original Assignee
Mitsubishi 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 Mitsubishi Aluminum Co Ltd filed Critical Mitsubishi Aluminum Co Ltd
Priority to JP12272081A priority Critical patent/JPS5825452A/en
Publication of JPS5825452A publication Critical patent/JPS5825452A/en
Publication of JPH028018B2 publication Critical patent/JPH028018B2/ja
Granted legal-status Critical Current

Links

Abstract

PURPOSE:To provide the titled alloy consisting of a prescribed percentage each of Zr and Si and the balance Al with inevitable impurities, showing superior dropping resistance during heating in a brazing stage, and preventing the corrosion of a tube material as the opposite member by the superior sacrificial anode effect. CONSTITUTION:This Al alloy for the fin material of a heat exchanger consists of, by weight 0.02-0.2% Zr, 0.2-1.0% Si and the balance Al with inevitable impurities or contains further 0.1-0.7% Mg. Since the Al alloy has superior dropping resistance and sacrificial anode effect, when it is used as the fin material of a heat exchanger made of Al alloy, the occurrence of fatigue and deformation during brazing is prevented. Accordingly, the heat exchanger can be manufactured in a high yield, and it shows superior corrosion resistance and can be used for over a long term.

Description

【発明の詳細な説明】 この発明は、特にAt合金製熱交換器のフィン材として
使用した場合、その製造に際して、真空ろう付けやフラ
ックスろう付けなどのろう付は工程の加熱に対してすぐ
れた耐垂下性(耐変形性)を示し、一方その実用に際し
ては、相手部材である管材をすぐれた犠牲陽極効果によ
りよく防食する特性を有するM合金に関するものである
[Detailed Description of the Invention] This invention particularly provides that when used as a fin material for an At alloy heat exchanger, brazing such as vacuum brazing and flux brazing is excellent against heating during the process. The present invention relates to an M alloy that exhibits sagging resistance (deformation resistance) and, when put into practical use, has the property of effectively preventing corrosion of a mating member, a tube material, due to its excellent sacrificial anode effect.

従来、一般にM合金製熱交換器は、フィン材として、例
えばAA−Mn合金の薄板、あるいはA1.−Mn合金
の芯材の片面あるいは両面にAN−8i系合金のろう材
をクラッドしたものからなるプレージングシートから成
形されたものを用意し、一方管材としては、例えば純A
AまたはAt−Mn系合金製のもの、あるいは純Mまた
はAe−Mn系合金の芯材の表面にAA−8i系合金の
ろう材をクラッドしたものからなるプレージングシート
で構成されたものを用意し、これら両部材を適宜組合せ
てろう付けすることによって製造されている。しかしな
がら、このように製造されている従来At合金製熱交換
器においては、その製造に際して、ろう付は時の高温加
熱によってフィン材の強度が著しく低下するようになる
ばかシでなく、ろう材中の81がフィン材中に拡散侵食
して耐垂下性を劣化させるようになるため、フィン材が
変形し、この結果管材にフィン材をうまくろり付けする
ことができなくなる問題がしばしば発生するものであり
、一方その実用に際しては、フィン材中のMnは、これ
を電気化学的に著しく責にする作用があるため、例えば
管材に純An系のものを使用した場合には、管材がフィ
ン材に比して卑になることから、管材の腐食が促進され
、この結果管材には貫通孔が形成されるようになシ、こ
の貫通孔に原因する事故の発生がしばしば見られるもの
であった。
Conventionally, M alloy heat exchangers have generally used a thin plate of AA-Mn alloy or A1. A plating sheet made of a Mn alloy core material clad with an AN-8i alloy brazing filler metal on one or both sides is prepared, while the tube material is made of, for example, pure A
Prepare a sheet made of A or At-Mn alloy, or a plating sheet made of pure M or Ae-Mn alloy core material clad with AA-8i alloy brazing material. However, it is manufactured by appropriately combining these two members and brazing them together. However, in manufacturing conventional At alloy heat exchangers manufactured in this way, brazing is not a process that significantly reduces the strength of the fin material due to high-temperature heating; 81 diffuses into the fin material and deteriorates its drooping resistance, which often causes the fin material to deform, making it impossible to properly braze the fin material to the pipe material. On the other hand, in practical use, Mn in the fin material has a significant electrochemical effect, so for example, if pure An-based pipe material is used, the pipe material may become attached to the fin material. In comparison, corrosion of the pipe material is accelerated because it is less noble, and as a result, through-holes are formed in the pipe material, and accidents often occur due to these through-holes.

そこで、フィン材にZnを含有させることによってフィ
ン材を管材に比して電気化学的に卑にし、この結果の犠
牲陽極効果によって管材を防食する試みもなされたが、
その製造に際して、真空ろう付けを適用した場合、この
真空ろう付は工程中にフィン材中のZnが蒸発し、ろう
付は後には管材に比して電気化学的に卑にするのに足る
Znがフィンいものであった。
Therefore, attempts have been made to make the fin material electrochemically less noble than the pipe material by incorporating Zn into the fin material, and to prevent corrosion of the pipe material using the resulting sacrificial anode effect.
When vacuum brazing is applied during the manufacturing process, the Zn in the fin material evaporates during the vacuum brazing process, and the brazing process later contains enough Zn to make it electrochemically base compared to the pipe material. It was a funny thing.

本発明者等は、−ヒ述のような観点から、ろう付けに際
しての加熱に対しても変形がなく、かつ管材に比して相
対的に電気化学的に卑な特性をもったAI!、合金製熱
交換器のフィン材を得べく研究を行々つた結果、前記フ
ィン材を、Zr:0.02〜0.2%、 Si: 0.
2〜1.0%を含有し、さらに必要に応じてMg :0
.1〜0.7%を含有し、残りがAlと不可避不純物か
らなる組成(以上重量%)を有するAt合金で構成する
と、前記フィン材は、Mnを含有しないために相対的に
電気化学的に責にならないことから、管材に対してすぐ
れた犠牲陽極効果を発揮し、かつ熱伝導性のすぐれた状
態に保持され、さらに合金成分たるZrとSiとの共存
によって、ろう付は時におけるろう材中の81のフィン
材中への拡散侵食が著しく抑制されるようになることが
ら、すぐれた耐垂下性をもつようになシ、また前記フィ
ン材がさらにMgを含有する場合には高強度を有したも
のになるという知見を得たのである。
From the viewpoints mentioned above, the present inventors have developed an AI that does not deform even when heated during brazing and has relatively less electrochemical properties than pipe materials! As a result of conducting research to obtain a fin material for an alloy heat exchanger, the fin material contained Zr: 0.02 to 0.2%, Si: 0.
Contains 2 to 1.0%, and further contains Mg: 0 as necessary.
.. When the fin material is composed of an At alloy having a composition (by weight %) containing 1 to 0.7% of Mn and the rest consisting of Al and unavoidable impurities, the fin material has a relatively low electrochemical performance because it does not contain Mn. It exhibits an excellent sacrificial anode effect on the pipe material and maintains excellent thermal conductivity, and due to the coexistence of Zr and Si, which are alloy components, brazing can be performed using a brazing material. Since the diffusion erosion into the fin material of 81 is significantly suppressed, it has excellent sagging resistance, and when the fin material further contains Mg, it has high strength. I gained the knowledge that it becomes what you have.

この発明は、上記知見にもとづいてなされたものであっ
て、以下に成分組成範囲を上記の通シに限定した理由を
説明する。
This invention was made based on the above knowledge, and the reason why the component composition range was limited to the above general range will be explained below.

(a)  Zr Zr成分は、フィン材のための薄板製造に際して、冷間
圧延と、300〜350℃付近の温度に加熱の中間焼鈍
との繰シ返し工程における前記中間焼鈍処理中に微細な
AP、−Zr化合物として析出し、とのAA−Zr化合
物は再結晶温度を著しく上昇させる作用があることから
、再結1碌の結晶粒は粗大化するようになり、この結果
管材とフィン材とのろう付は時にフィン材へのろう材中
のSiの拡散侵食が抑制されるようになシ、もって耐垂
下性をすぐれた状態に保持する作用をもつが、その含有
量が0.02%未満では所望のすぐれた耐垂下性を確保
することができず、一方0.2%を越えて含有させても
、よシ一層の向上効果が現われず、むしろ溶解鋳造時に
巨大晶を形成し易くなって加工性が損なわれるようにな
ることから5その含有量を0.02〜02%と定めた。
(a) Zr The Zr component forms fine AP particles during the intermediate annealing process in which cold rolling and intermediate annealing are heated to a temperature around 300 to 350°C. , -Zr compounds precipitate, and the AA-Zr compounds have the effect of significantly increasing the recrystallization temperature, so the crystal grains of the recrystallized grains become coarser, and as a result, the tube material and fin material Brazing sometimes suppresses the diffusion erosion of Si in the brazing filler metal to the fin material, thereby maintaining excellent sagging resistance, but its content is 0.02%. If the content is less than 0.2%, it will not be possible to secure the desired excellent sagging resistance, while if the content exceeds 0.2%, no further improvement will be achieved, and instead, giant crystals will be likely to form during melting and casting. Therefore, the content was set at 0.02 to 02%.

(b)   5i Si成分には、AP!−Zr化合物の形成を著しく促進
し、もって耐垂下性を向上させる作用があるが、その含
有量が0.2%未満では前記作用に所望の効果が得られ
ず、一方1.0 %を越えて含有させても、よシ一層の
向上効果が現われないばかりでなく、むしろ電気化学的
に責になる傾向が現われ、犠牲陽極効果を十分発揮でき
なくなることから、その含有量を0.2〜1.0%と定
めた。
(b) 5i Si component has AP! - It has the effect of significantly accelerating the formation of Zr compounds and thereby improving the sagging resistance, but if the content is less than 0.2%, the desired effect cannot be obtained, whereas if it exceeds 1.0%. Even if it is contained, not only will it not produce any further improvement effect, but it will also have a tendency to become electrochemically detrimental, making it impossible to fully demonstrate the sacrificial anode effect. It was set at 1.0%.

(c)  Mg Mg成分には、素地に固溶して、これを固溶強化し、か
つ薄板製造に際しての中間焼鈍後の冷間加工時にわずか
な加工率で、これを加工硬化させて強度を著しく向上さ
せる作用があるので、特に強度が要求される場合に必要
に応じて含有されるが、その含有量が0.1%未満では
所望の強度向上効果が得られず、一方0.7チを越えて
含有させると、再結晶粒粗大化作用が阻害されるように
なって耐垂下性が劣化することから、その含有量を0.
1〜0.7%と定めた。
(c) Mg The Mg component is solid-solved in the base material to strengthen it as a solid solution, and is work-hardened at a small processing rate during cold working after intermediate annealing during thin plate manufacturing to increase strength. Since it has the effect of significantly improving strength, it is included as necessary when particularly high strength is required, but if the content is less than 0.1%, the desired strength improvement effect cannot be obtained; If the content exceeds 0.05%, the recrystallized grain coarsening effect will be inhibited and the sagging resistance will deteriorate.
It was set at 1% to 0.7%.

つぎに、この発明のA2合金を実施例にょシ従来例と対
比しながら具体的に説明する。
Next, the A2 alloy of the present invention will be specifically explained by comparing it with an example and a conventional example.

実施例 通常の溶解法により、それぞれ第1表に示される最終成
分組成をもったフィン材用本発明A9合金1〜4.フィ
ン材用従来Ae合金1,2.管材用Ae金合金、b、お
よびろう材用A9合金を溶製し、鋳造して鋳塊とした。
Examples A9 alloys 1 to 4 of the present invention for fin materials having the final component compositions shown in Table 1 were prepared by a conventional melting method. Conventional Ae alloys for fin materials 1, 2. Ae gold alloy for pipe materials, b, and A9 alloy for brazing filler metal were melted and cast into ingots.

なお、第1表には表示を省略したが、これらの各種AP
、合金鋳塊は、いずれも不可避不純物として、Mn:0
.01%以下、Mg:0.01チ以下、 cu: o、
o 5 %以下、Zn:O,,02%以下。
Although not shown in Table 1, these various APs
, alloy ingots all contain Mn: 0 as inevitable impurities.
.. 01% or less, Mg: 0.01% or less, cu: o,
o 5% or less, Zn:O, 02% or less.

Fe: 0.40 %以下、およびCr: 0.01%
以下を含有するものであった。
Fe: 0.40% or less, and Cr: 0.01%
It contained the following:

ついで、この結果得られた各種の上記M合金鋳塊につい
て、本発明AQ合金1〜4.従来合金l。
Next, regarding the various above-mentioned M alloy ingots obtained as a result, AQ alloys 1 to 4 of the present invention. Conventional alloy l.

2、管材用A9合金a、bは熱間圧延にょシ板厚:S 
+Otの熱延板とし、またろう材用超合金は同様に熱間
圧延によシ板厚:5rtatの熱延板とし、さらに前記
ろう材用A2合金の熱延板には冷間圧延を施して板厚:
1朋の冷延板とした。
2. A9 alloys a and b for pipe materials are hot-rolled plate thickness: S
A hot-rolled plate of +Ot was used, and the superalloy for brazing metal was similarly hot-rolled and a hot-rolled plate with a thickness of 5rtat, and the hot-rolled plate of the A2 alloy for brazing metal was cold-rolled. Thickness:
It was made into a cold-rolled sheet of 1.

この状態で、本発明A1合金1−4.従来M合金1.2
.および管材用AR金合金、bの熱延板の両面に、それ
ぞれ上記ろう材用A9合金の冷延板を重ね合せ、熱間圧
延にて両面クラッドすると共に、本発明At合金1〜4
および従来A1合金1,2のクラツド材については、そ
の板厚−を0.5mmとし、一方管材用AA合金a、b
については、その板厚を1龍とし、さらに本発明ATL
合金1〜4および従来A1合金1,2のクラツド材の一
部には冷間圧延を施し、この工程中に中間焼鈍を施して
40%の冷延率を有する最終板厚:0.16gのプレー
ジングシートとした。
In this state, the present invention A1 alloy 1-4. Conventional M alloy 1.2
.. The cold-rolled plates of the A9 alloy for brazing filler metal are laminated on both sides of the hot-rolled plates of the AR gold alloy for pipe materials and b, and both sides are clad by hot rolling, and the At alloys 1 to 4 of the present invention
For the conventional A1 alloys 1 and 2 cladding materials, the plate thickness was set to 0.5 mm, while the AA alloys a and b for pipe materials were
, the plate thickness is 1 dragon, and the present invention ATL
A part of the clad material of Alloys 1 to 4 and conventional A1 Alloys 1 and 2 was cold rolled, and intermediate annealing was performed during this process to obtain a final plate thickness of 0.16 g with a cold rolling reduction of 40%. It was used as a praising sheet.

また、一方上記の板厚:8朋を有する本発明At合金1
〜4.従来超合金1,2.および管材用Aε合金a、b
の熱延板に冷間圧延を施し、本発明A1合金1〜4およ
び従来A2合金1.2の熱延板については、その板厚を
0.5Bとし、管材用A9合金abの熱延板については
、その板厚を1朋とし、さらに本実tag合金ト4およ
び従来超合金1,2の冷延板の一部には冷間圧延を続け
て施し、途中中間焼鈍を施して40%冷延率を有する最
終板厚:O,16Bの薄板とした。
Moreover, on the other hand, the present invention At alloy 1 having the above plate thickness: 8 mm
~4. Conventional superalloys 1, 2. and Aε alloys a, b for pipe materials
The hot-rolled sheets of the A1 alloys 1 to 4 of the present invention and the conventional A2 alloy 1.2 have a thickness of 0.5B, and the hot-rolled sheets of the A9 alloy ab for pipe materials are , the plate thickness was set to 1 mm, and a part of the cold rolled plates of real tag alloy 4 and conventional superalloys 1 and 2 were continuously cold rolled, and intermediate annealing was performed in the middle to reduce the thickness to 40%. A thin plate having a cold rolling rate and a final plate thickness of O, 16B was obtained.

このようにして調製された板厚:0.16m、および0
.5@Ilを有する本発明A1合金1〜4および従来超
合金1,2とろう材用超合金とのクラツド材であるフィ
ン材用プレージングシート(以下本発明フィン材用プレ
ージングシートト4および従来フィン材用プレージング
シート1,2という)、板厚:1間を有する管材用超合
金a、 bとろう材用A1合金とのクラツド材である管
材用ブレージングシー)a、−b、さらに上記の板厚:
0.16朋および0−511+1を有すb本発明フィン
材用薄板1〜4および従来フィン材用薄板1,2.そし
て上記の板厚:1關を有する管材用薄板a、 bのうち
、板厚:O,16,、、、の本発明フィン材用プレージ
ングシート1〜4および従来フィン材用プレージングシ
ート1,2.さらに同0.1611の本発明フィン材用
薄板1−4および従来フィン材用薄板について、これよ
シ切シ出した幅:3011X長さ:14oIHの寸法を
有する試験片を用い、この試験片の長さ方向−刃端部3
0朋を水平固定した状態で、温度二620℃に5分間保
持の条件で耐垂下性試験を行ない、加熱後の試験片の先
端部における垂下高さを測定した。この測定結果を第2
表に示した。
The plate thickness thus prepared: 0.16 m, and 0
.. 5@Il and conventional superalloys 1 and 2 and brazing superalloys (hereinafter referred to as plating sheets for fin materials of the present invention 4 and 4). Conventional brazing sheets for fin materials 1 and 2), brazing sheets for pipe materials which are clad materials of superalloys a and b for pipe materials having a plate thickness of 1 and A1 alloy for brazing filler metals) a, -b, and Above board thickness:
0.16 and 0-511+1 b The thin plates 1 to 4 for fin materials of the present invention and the thin plates 1, 2 for conventional fin materials. Among the thin plates a and b for pipe materials having a thickness of 1, the plating sheets 1 to 4 for fin materials of the present invention and the conventional plating sheet 1 for fin materials of the present invention have thicknesses of O, 16, ... ,2. Furthermore, using a test piece having dimensions of width: 3011 x length: 14 o IH cut out from the thin plate 1-4 for fin material of the present invention and the conventional thin plate for fin material of the same 0.1611, Length direction - blade end 3
A drooping resistance test was conducted under the condition that the specimen was held horizontally at 2,620° C. for 5 minutes, and the height of drooping at the tip of the test piece after heating was measured. This measurement result is
Shown in the table.

第2表に示されるように、本発明フィン材用プレージン
グシートト4および本発明フィン材用薄板1〜4は、い
ずれもすぐれた耐垂下性を示し、ろう付は時に”へたシ
”や変形の発生がほとんどなく、良好なろう付けが可能
であることを示すのに対して、従来フィン材用プレージ
ングシートl。
As shown in Table 2, the plating sheet 4 for fin materials of the present invention and the thin plates 1 to 4 for fin materials of the present invention both exhibit excellent droop resistance, and brazing sometimes causes "sagging". This shows that there is almost no occurrence of deformation or deformation, indicating that good brazing is possible, whereas conventional plating sheets for fin materials l.

2および従来フィン材用薄板1,2では耐垂下性の劣っ
たものになっている。
2 and the conventional thin plates 1 and 2 for fin materials have poor droop resistance.

ついで、上記の板厚0.5I+1mを有する本発明フィ
ン材用プレージングシート1〜4および従来Zイン材用
プレージングシート1,2.さらに板厚二〇・51mを
有する本発明フィン材用薄板1〜4および従来フィン材
用薄板1,2から幅:4o1RHX長さニア0朋のフィ
ン材用試験片を切シ出し、一方板厚:1朋を有する管材
用プレージングシートa。
Next, plating sheets 1 to 4 for fin materials of the present invention and conventional plating sheets 1, 2 for Z-in materials having the above-mentioned plate thickness of 0.5I+1m were prepared. Furthermore, test pieces for fin materials having a width of 4 o 1 RH x length of near 0 mm were cut out from the thin plates 1 to 4 for fin materials of the present invention having a plate thickness of 20.51 m and the thin plates 1 and 2 for conventional fin materials. :1 plating sheet for pipe material a.

b、および同I IINの管材用薄板a、bからは幅:
第   2   表 5011X長さニア0龍の寸法をもった管材用試験片を
切り出し、この管材用試験片の長さ方向中心部に、前記
フィン材用試験片をそれぞれ垂直に配置して組合せ(こ
の場合フィン材用試験片か管材用試験片のいずれか一方
にろう材をクラッドしたプレージングシートを組合わせ
る)、この状態で真空中、温度:620℃に5分間保持
の条件でろう付けを行ない、10 p、p、BのCu 
 イオンを添加した40℃の水道水中に30日間浸漬の
水道水浸漬試験と、30日間のCASS試験に供した。
b, and the width from the pipe material thin plates a and b of I IIN:
Table 2 A tube material test piece having dimensions of 5011 In this case, either the fin material test piece or the tube material test piece is combined with a brazing sheet clad with a brazing material), and in this state, brazing is performed in a vacuum at a temperature of 620°C for 5 minutes. , 10 p, p, B of Cu
It was subjected to a tap water immersion test in which it was immersed in tap water at 40°C to which ions had been added for 30 days, and a CASS test for 30 days.

これらの試験後、上記管材用試験片における孔食数およ
び最大孔食深さを測定し、この測定結果を第3表に示し
た。
After these tests, the number of pitting corrosion and the maximum pitting depth in the above tube material test pieces were measured, and the measurement results are shown in Table 3.

第3表に示されるように、本発明フィン材用プレージン
グシート1〜4および本発明フィン材用薄板1〜4は、
いずれも犠牲陽極効果を十分発揮することから、相手材
である管材用薄板al  blおよび管材用ブレージン
グシー)a、bの腐食が最小に抑えられているのに対し
て、従来フィン材プレージングシート1,2および従来
フィン材用薄板1,2では、これらが電飯化学的に責で
あることから、相手材の腐食がかえって促進されている
ことが明らかである。
As shown in Table 3, plating sheets 1 to 4 for fin materials of the present invention and thin plates 1 to 4 for fin materials of the present invention are as follows:
Both of them fully exhibit the sacrificial anode effect, so corrosion of the mating materials, thin plate for pipes (Al BL) and brazing seams for pipes (a) and b), is suppressed to a minimum, whereas conventional fin material plating sheets 1 and 2 and the conventional thin plates 1 and 2 for fin materials, it is clear that corrosion of the mating material is accelerated because these are chemically harmful to the metal.

上述のように、この発明のAffiff上、すぐれた耐
垂下性と犠牲陽極効果を、有しているので、これをAt
合金製熱交換器のフィン材として使用すれば、ろう付は
時に“へた!ll#や変形の発生なく、したカiつて歩
留りよく熱交換器を製造することができ、しかもこの結
果の熱交換器はすぐれた耐食性を有し、長期に亘る使用
が可能となるなど工業上有用な特性を有するのである。
As mentioned above, the Affiff of this invention has excellent droop resistance and sacrificial anode effect, so it can be used as At
When used as a fin material for an alloy heat exchanger, brazing can produce heat exchangers with a higher yield without causing "deformation" or deformation, and the resulting heat The exchanger has excellent corrosion resistance and has industrially useful properties such as being able to be used for a long period of time.

出願人  三菱アルミニウム株式会社 代理人  富  1) 和  夫Applicant: Mitsubishi Aluminum Corporation Agent Tomi 1) Kazuo

Claims (2)

【特許請求の範囲】[Claims] (1)  Zr: 0.02〜0.2%、 Si : 
0.2〜1.Oqbを含有し、残りがAtと不可避不純
物からなる組成(以上重量%)を有することを特徴とす
る耐垂下性および犠牲陽極効果にすぐれた熱交換器フィ
ン材用M合金。
(1) Zr: 0.02-0.2%, Si:
0.2-1. An M alloy for heat exchanger fin material having excellent sagging resistance and sacrificial anode effect, characterized by containing Oqb and the remainder consisting of At and unavoidable impurities (weight percent).
(2)  Zr: 0.02〜0.2 %、 Si: 
0.2〜1.0 %を含有し、さらにMg : O,l
 −0,7%を含有し、残シがAtと不可避不純物から
なる組成(以上重量%)を有することを特徴とする耐垂
下性および犠牲陽極効果にすぐれた熱交換器フィン材用
At合金。
(2) Zr: 0.02-0.2%, Si:
Contains 0.2 to 1.0%, and further contains Mg: O, l
An At alloy for heat exchanger fin material having excellent sagging resistance and sacrificial anode effect, characterized in that it contains -0.7% and the remainder consists of At and unavoidable impurities (weight percent).
JP12272081A 1981-08-05 1981-08-05 Al alloy for fin material of heat exchanger with superior dropping resistance and sacrificial anode effect Granted JPS5825452A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP12272081A JPS5825452A (en) 1981-08-05 1981-08-05 Al alloy for fin material of heat exchanger with superior dropping resistance and sacrificial anode effect

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP12272081A JPS5825452A (en) 1981-08-05 1981-08-05 Al alloy for fin material of heat exchanger with superior dropping resistance and sacrificial anode effect

Publications (2)

Publication Number Publication Date
JPS5825452A true JPS5825452A (en) 1983-02-15
JPH028018B2 JPH028018B2 (en) 1990-02-22

Family

ID=14842915

Family Applications (1)

Application Number Title Priority Date Filing Date
JP12272081A Granted JPS5825452A (en) 1981-08-05 1981-08-05 Al alloy for fin material of heat exchanger with superior dropping resistance and sacrificial anode effect

Country Status (1)

Country Link
JP (1) JPS5825452A (en)

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS55119148A (en) * 1979-03-09 1980-09-12 Furukawa Alum Co Ltd Alominum alloy with excellent strength and moldability
JPS5616646A (en) * 1979-07-23 1981-02-17 Sumitomo Light Metal Ind Ltd Aluminum alloy clad for heat exchanger
JPS5641347A (en) * 1979-09-13 1981-04-18 Furukawa Alum Co Ltd Aluminum alloy clad for vacuum brazing

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS55119148A (en) * 1979-03-09 1980-09-12 Furukawa Alum Co Ltd Alominum alloy with excellent strength and moldability
JPS5616646A (en) * 1979-07-23 1981-02-17 Sumitomo Light Metal Ind Ltd Aluminum alloy clad for heat exchanger
JPS5641347A (en) * 1979-09-13 1981-04-18 Furukawa Alum Co Ltd Aluminum alloy clad for vacuum brazing

Also Published As

Publication number Publication date
JPH028018B2 (en) 1990-02-22

Similar Documents

Publication Publication Date Title
JPS6248742B2 (en)
US20210394313A1 (en) Aluminum alloy brazing sheet and manufacturing method thereof
JP2010270387A (en) Aluminum alloy fin material for heat exchanger and method for producing the same
JPH0210212B2 (en)
JPS60138037A (en) Al alloy composite fin material for heat exchanger having excellent high-temperature strength and sacrificial anode effect
JPS59116353A (en) Composite al alloy sheet for fin material for heat exchanger
JPS5825452A (en) Al alloy for fin material of heat exchanger with superior dropping resistance and sacrificial anode effect
JPH01102297A (en) Aluminum alloy compound fin material for heat exchanger suitable for brazing and corrosion resistance
JPH07179973A (en) Al alloy brazing sheet for vacuum brazing for structural member for heat exchanger, excellent in corrosion resistance
JPS58164749A (en) Composite al alloy material with superior pitting corrosion resistance
JPH01159343A (en) Al alloy clad fin material for heat exchanger having superior brazability and corrosion resistance
JPH11140572A (en) High strength aluminum alloy brazing sheet for heat exchanger excellent in intergranular corrosion resistance
JPH06145862A (en) Heat exchanger made of al alloy constituted of high strength fin material
JPH0210216B2 (en)
JPH029100B2 (en)
JPS5985838A (en) Al alloy for fin material of heat exchanger having superior sag resistance and sacrificial anode effect
JPS6078188A (en) Composite pipe material for heat exchanger made of al alloy having excellent hole corrosion resistance
JPS6261661B2 (en)
JPH025569B2 (en)
JPH0352549B2 (en)
JPH0288740A (en) High strength al alloy clad material for structural member of heat exchanger having excellent pitting corrosion resistance with which working fluid is brought into contact
JPS60110835A (en) Al alloy brazing sheet having significant sacrificial anode effect
JPH0299325A (en) High strength al alloy clad material for working fluid contact structural member of heat exchanger excellent in pitting resistance
JPH03162543A (en) High strength brazing sheet for al heat exchanger structural member
JP2000087168A (en) Aluminum alloy clad material for automotive heat exchanger excellent in corrosion resistance in alkaline environment