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JPS63293136A - Aluminum alloy and aluminum alloy clad material for heat exchanger member - Google Patents

Aluminum alloy and aluminum alloy clad material for heat exchanger member

Info

Publication number
JPS63293136A
JPS63293136A JP13077087A JP13077087A JPS63293136A JP S63293136 A JPS63293136 A JP S63293136A JP 13077087 A JP13077087 A JP 13077087A JP 13077087 A JP13077087 A JP 13077087A JP S63293136 A JPS63293136 A JP S63293136A
Authority
JP
Japan
Prior art keywords
alloy
aluminum alloy
brazing
core material
heat exchanger
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
JP13077087A
Other languages
Japanese (ja)
Inventor
Kunihiko Kishino
邦彦 岸野
Motoyoshi Yamaguchi
山口 元由
Katsutoshi Sasaki
佐々木 勝敏
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 JP13077087A priority Critical patent/JPS63293136A/en
Publication of JPS63293136A publication Critical patent/JPS63293136A/en
Pending legal-status Critical Current

Links

Abstract

PURPOSE:To obtain the titled Al alloy which shows high strength, excellent brazability and corrosion resistance by incorporating specific ratios of Mg, Si, Fe, Cu and Ni to the alloy and furthermore incorporating one or more kinds from either or both groups between the one of Mn, Cr, Zr, etc., and the other of Zn, In and Sn thereto. CONSTITUTION:The Al alloy for an exchanger member contg., by weight, 0.01-1% Mg, 0.01-1.5% Si, 0.01-1.0% Fe, 0.05-2% Cu and 0.6-5% Ni and furthermore contg. one or more kinds of elements from either or both groups between the one of 0.01-2% Mn, 0.001-0.5% Cr, 0.001-0.5% Zr, 0.001-1.5% Hf, 0.001-0.5% Ti and 0.0001-0.1% B and the other of 0.5-5% Zn, 0.005-0.5% In and 0.005-0.5% Sn is provided. Said Al alloy has good brazability and has excellent strength after brazing. The Al alloy clad material for a heat exchanger member in which said Al alloy is formed to the core and in which the Al alloy wax material contg. >=5wt.% Si and clad on either face or both faces thereof has the excellent characteristics as well equal to said Al alloy.

Description

【発明の詳細な説明】 〔産業上の利用分野〕 本発明はろう付により製造される熱交換器部材用アルミ
ニウム合金および該合金を芯材とした合わせ材に関する
ものであり、特に強度の優れたものである。
[Detailed Description of the Invention] [Field of Industrial Application] The present invention relates to an aluminum alloy for heat exchanger components manufactured by brazing and a composite material using the alloy as a core material, and particularly relates to an aluminum alloy with excellent strength. It is something.

〔従来の技術〕[Conventional technology]

従来熱交換器、特に自動車用熱交換器であるラジェータ
ー、ヒーター、オイルクーラーおよびエアコン用のエバ
ポレータ、コンデンサ等の多くはAl合金製であり、所
望の形状に成形後組み付け、ろう付により接合されてい
る。これら熱交換器用の材料としては第1表に示すAl
又はAl合金がある。
Conventional heat exchangers, especially automotive heat exchangers such as radiators, heaters, oil coolers, evaporators for air conditioners, condensers, etc., are mostly made of Al alloys, which are molded into the desired shape and then assembled and joined by brazing. There is. The materials for these heat exchangers include Al shown in Table 1.
Or there is an Al alloy.

これらのAl又はAl合金を単独で使用する場合として
はエアコン用熱交換器の押出多穴チューブ、積層タイプ
のエバポレータやオイルクーラーのフィンあるいはオー
ルAiタイプのラジェーターの配管等があり、さらにこ
れらのAl又はAl合金を合わせ材として使う場合は第
2表に示すようなアルミニウム合金ろう材を皮材とし第
1表のAl又はAl合金芯材の片面あるいは両面にクラ
ッドしたプレージングシートが用いられる。
Examples of when these Al or Al alloys are used alone include extruded multi-hole tubes for air conditioner heat exchangers, fins for laminated type evaporators and oil coolers, and piping for all-Ai type radiators. Alternatively, when an Al alloy is used as a laminating material, a plating sheet is used in which the aluminum alloy brazing material shown in Table 2 is used as the skin material and the Al or Al alloy core material shown in Table 1 is clad on one or both sides.

上記のプレージングシートの使用例としてはエアコン用
熱交換器のフィン材、積層タイプのエバポレータやオイ
ルクーラーのシート材及びラジェーターのチューブ、ヘ
ッダーあるいはタンク材等があり、さらにラジェーター
のチューブ、ヘッダー材では冷却水または冷却液の流れ
る部材内部の耐食性向上のために冷却水または冷却液と
接触するプレージングシートの面に芯材より電位の低い
犠牲陽極層を設けて貫通孔食の発生を防止している材料
も使用されている。
Examples of the use of the above plating sheets include fin materials for air conditioner heat exchangers, sheet materials for laminated type evaporators and oil coolers, radiator tubes, headers, and tank materials. In order to improve the corrosion resistance inside the parts through which the cooling water or cooling liquid flows, a sacrificial anode layer with a lower potential than the core material is provided on the surface of the plating sheet that comes into contact with the cooling water or cooling liquid to prevent the occurrence of through-pitting corrosion. Other materials are also used.

また家庭用や業務用エアコン等の熱交換器のフィン材に
もAl合金が使われている。
Al alloys are also used as fin materials for heat exchangers in home and commercial air conditioners.

[発明が解決しようとする問題点] このような熱交換器においては最近軽量化。[Problem to be solved by the invention] Recently, the weight of such heat exchangers has been reduced.

低コスト化の目的から各構成部材の薄肉化の要求が高ま
っており、これを実現するためより高強度な材料が求め
られ種々の合金開発が試みられている。しかし、熱交換
器用部材、特にろう付により製造される部材は約600
℃に加熱されるろう付時の強度及びろう付後の強度が共
に高く、かつろう付時に7ラツクスを使用する場合はフ
ラックスとの反応がないこと、さらにろう付後において
は耐食性をも要求される等、種々の性能を全て合わせも
つ必要があるためいまだ満足すべき材料が得られていな
い。
In order to reduce costs, there is an increasing demand for thinner components, and in order to achieve this, materials with higher strength are required, and various alloys are being developed. However, there are approximately 600 parts for heat exchangers, especially parts manufactured by brazing.
The strength during brazing heated to ℃ and the strength after brazing are both high, and if 7lux is used during brazing, there is no reaction with flux, and corrosion resistance is also required after brazing. Since it is necessary to have all of the various performances such as

〔問題点を解決するための手段〕[Means for solving problems]

本発明はこれに鑑み種々検討の結果、ろう付性が良好で
あり、かつろう付後の強度も優れた熱交換器部材用アル
ミニウム合金及びアルミニウム合金合わせ材を開発した
ものである。
In view of this, as a result of various studies, the present invention has developed aluminum alloys and aluminum alloy composite materials for heat exchanger members that have good brazing properties and excellent strength after brazing.

即ち本発明アルミニウム合金はM =j 0.01〜1
wt%、 3 i 0.01〜1.5 wt%、 Fe
0.01〜1.0wt%、 cuo、os 〜2wt%
、 N io、6〜5wt%を含み、さらにMn0.0
1〜2wt%、 cro、001〜0.5wt%、 Z
 ro、001〜0.5 Wj%、 Hf0.001〜
1.5 wt%、 T ! 0.001〜0.5 wt
%、 80.0001〜0.1 wt%とZn0.5〜
5wt%、  In0.005〜0.5wt%、 S 
n0.005〜0.5 wt%のいずれが一方または両
方の群よりそれぞれ1種もしくは2種以上の元素を含み
、残部Alと不可避的不純物からなることを特徴とする
ものである。
That is, the aluminum alloy of the present invention has M = j 0.01 to 1
wt%, 3i 0.01-1.5 wt%, Fe
0.01-1.0wt%, cuo, os ~2wt%
, Nio, 6 to 5 wt%, and further Mn0.0
1-2wt%, cro, 001-0.5wt%, Z
ro, 001~0.5 Wj%, Hf0.001~
1.5 wt%, T! 0.001~0.5wt
%, 80.0001~0.1 wt% and Zn0.5~
5wt%, In0.005~0.5wt%, S
It is characterized in that any of n0.005 to 0.5 wt% contains one or more elements from one or both groups, and the remainder consists of Al and inevitable impurities.

また本発明アルミニウム合金合わせ材の1つは上記アル
ミニウム合金を芯材とし、該芯材の片面または両面に3
15wt%以上含むアルミニウム合金ろう材をクラッド
することを特徴とするものである。
In addition, one of the aluminum alloy laminated materials of the present invention uses the above-mentioned aluminum alloy as a core material, and has three layers on one or both sides of the core material.
It is characterized by being clad with an aluminum alloy brazing filler metal containing 15 wt% or more.

さらに本発明アルミニウム合金合わせ材の他の1つは上
記アルミニウム合金を芯材とし該芯材の片面または両面
に芯材よりも50mV以上卑な電位を有するアルミニウ
ム合金をクラッドすることを特徴とするものである。
Furthermore, another one of the aluminum alloy laminated materials of the present invention is characterized in that the above-mentioned aluminum alloy is used as a core material, and one or both sides of the core material is clad with an aluminum alloy having a potential 50 mV or more more base than the core material. It is.

〔作 用〕[For production]

本発明においてAl合金の成分組成を上記の如く限定し
たのは以下の理由による。
The reason why the composition of the Al alloy is limited as described above in the present invention is as follows.

Mgの添加はマトリックスに固溶すると共にSiと共に
MgzSiの微細な析出物を生成し強度の向上に寄与す
るもので、Mg含有母を0、01〜1wt%と限定した
のは0.01wt%未満では十分な強度が1qられず、
1wt%を超えるとろう付性を著しく阻害し、甚だしい
場合はろう付不能になるからであり、より望ましくは0
.02〜0.6wt%の範囲が良好であり、フラックス
を使用するろう付の場合は0.02〜0.3wt%の範
囲での添加が望ましい。
The addition of Mg dissolves in the matrix and forms fine precipitates of MgzSi together with Si, contributing to the improvement of strength, and the Mg-containing matrix is limited to 0.01 to 1 wt% to less than 0.01 wt%. In this case, sufficient strength cannot be obtained by 1q,
This is because if it exceeds 1 wt%, brazing properties will be significantly inhibited, and in extreme cases, brazing will become impossible.More preferably, 0%
.. A range of 0.02 to 0.6 wt% is good, and in the case of brazing using flux, addition in a range of 0.02 to 0.3 wt% is desirable.

Slの添加はMgと共にMg2 S iの微細な析出物
を生成し、Mnが添加される場合はさらにAl−1vl
n−s i系の微細な析出物を生じ強度を向上させるも
ので、Si含有量を0.01〜1.5wt%と限定した
のは0.01wt%未満では十分な強度が得られず1.
5 wt%を超えるとろう付加熱時に溶融する危険性が
高くなるからである。
Addition of Sl produces fine precipitates of Mg2Si together with Mg, and when Mn is added, further Al-1vl
The Si content is limited to 0.01 to 1.5 wt% because sufficient strength cannot be obtained with less than 0.01 wt%. ..
This is because if it exceeds 5 wt%, there is a high risk of melting during brazing heating.

Feの添加は材料の強度、特に高温強度を向上させるも
ので、Fe含有mを0.01〜1.0 wt%と限定し
たのは0.01vt%未満では十分な強度が得られず1
.0wt%を超えると粗大なA!!−Fe−8i系また
はAi−Fe−xr系の金属間化合物を生じて強度を低
下させるからである。
The addition of Fe improves the strength of the material, especially the high-temperature strength, and the reason why the Fe content m is limited to 0.01 to 1.0 wt% is because sufficient strength cannot be obtained with less than 0.01 vt%.
.. If it exceeds 0wt%, it is a gross A! ! This is because -Fe-8i-based or Ai-Fe-xr-based intermetallic compounds are generated and the strength is reduced.

Cuの添加はAJ!−Cu系及びAl−Cu−Mg系の
0.P、ゾーンを析出し材料の強度、特に常温での強度
向上に寄与するもので、Cu含有Mを0.05〜2wt
%と限定したのは0.05wt%未満では上記効果が十
分ではなく、2wt%を超えるとろう付加熱時に溶融す
る危険が高くなり、かつ製品の耐食性が低下するからで
ある。
Addition of Cu is AJ! -Cu type and Al-Cu-Mg type 0. P, contributes to improving the strength of the material, especially at room temperature, by precipitating zones, and Cu-containing M is added in an amount of 0.05 to 2wt.
% because if it is less than 0.05 wt %, the above effect will not be sufficient, and if it exceeds 2 wt %, there will be a high risk of melting during brazing heating and the corrosion resistance of the product will be reduced.

Niの添加はA、esNiの微細な析出物を生じ、材料
の常温及び高温強度を向上させ、さらに耐食性や疲労強
度をも向上させるもので、Ni含有量を0.6〜5wt
%と限定したのは0.6wt%未満ではこれらの効果が
十分ではなく5wt%を超えると材料の延性を低下させ
るからである。
The addition of Ni produces fine precipitates of A, esNi, which improves the room temperature and high temperature strength of the material, and also improves the corrosion resistance and fatigue strength.
% because these effects are not sufficient if it is less than 0.6 wt%, and if it exceeds 5 wt%, the ductility of the material is reduced.

さらにMn0.01〜2wt%、 Cr0.001〜0
.5wt%、 Z r0.ool 〜0.5 wt%、
 Hf0.001〜1.5 wt%、 T i 0.0
01〜0.5 wt%、80.0001〜O5i wt
%とZn0.5〜5wt%、  In0.005〜0.
5wt%、 S no、005〜0.5 wt%のいず
れか一方または両方の群よりそれぞれ1種もしくは2杯
以上の元素を添加するのは、第1の群、即ちMn、Cr
、Zr、Hf、TiおよびBはいずれも微細かつ安定な
晶出物や析出物を生じ材料の組織を均一にする効果を有
し、その結果材料の強度特に高温強度及び延性の向上に
寄与するものでそれぞれの含有量を上記の如く限定した
のはその量を超えると材料の製造において鋳造時に粗大
な金属間化合物を生じて材料の延性及び靭性を低下させ
るからであり、下限未満では十分な効果を得られないか
らである。
Furthermore, Mn0.01~2wt%, Cr0.001~0
.. 5wt%, Zr0. ool ~0.5 wt%,
Hf0.001-1.5 wt%, T i 0.0
01~0.5 wt%, 80.0001~O5i wt
% and Zn0.5-5wt%, In0.005-0.
5 wt%, S no, 005 to 0.5 wt%, one or more elements from either or both groups are added to the first group, that is, Mn, Cr.
, Zr, Hf, Ti, and B all have the effect of producing fine and stable crystallized substances and precipitates and making the structure of the material uniform, and as a result, contribute to improving the strength of the material, especially the high-temperature strength and ductility. The reason why the content of each of these is limited as above is that if the content exceeds the above limit, coarse intermetallic compounds will be generated during casting during material production, reducing the ductility and toughness of the material. This is because no effect can be obtained.

なおこれら元素は単独で添加しても有効であるが複合添
加した場合はより一層良好な効果を有する場合が多い。
It should be noted that these elements are effective even when added alone, but often have even better effects when added in combination.

しかしこれらの元素は組織を均一化すると共に組織を微
細化するため、このような合金をフィン材等に使用する
場合、その組織が微細になり過ぎるとろう付時にろう材
と接触した部位でろう材中の3iが材料中に異常拡散し
その結果材料が座屈変形してしまう。
However, these elements make the structure uniform and make it finer, so when such an alloy is used for fin materials, etc., if the structure becomes too fine, it will cause problems in areas that come into contact with the filler metal during brazing. 3i in the material is abnormally diffused into the material, resulting in buckling deformation of the material.

従ってSiの拡散が問題となる部材に本発明材を使用す
る場合はこれらの元素の添加量は必要最小限に抑えるべ
きである。
Therefore, when the present invention material is used in a member in which Si diffusion is a problem, the amount of these elements added should be kept to the minimum necessary.

また上記の第2の群、即ちzn、Inおよびsnはいず
れも材料の電位を卑にする効果を有するため本発明材を
犠牲効果の必要な部位として使用する場合に耐孔食性を
向上させるものでそれぞれの含有量を上記の如く限定し
たのはその量を超えるとこの効果は飽和してしまい、さ
らに材料の延性を低下させる恐れを有するからであり、
下限未満ではその効果は十分ではないからである。なお
これらの元素は単独で添加しても2種以上を複合添加し
ても良い。
In addition, the second group, ie, zn, In, and sn, all have the effect of making the potential of the material base, so they improve the pitting corrosion resistance when the present invention material is used as a part that requires a sacrificial effect. The reason why the content of each is limited as above is because if the amount exceeds this amount, this effect will be saturated and there is a risk of further reducing the ductility of the material.
This is because the effect is not sufficient below the lower limit. Note that these elements may be added singly or in combination of two or more.

これら第1の元素群および第2の元素群については使用
される部位に応じていずれか、あるいは両方の元素群の
中より選ばれる1種もしくは2種以上の元素を添加すべ
きである。
For these first element group and second element group, one or more elements selected from either or both element groups should be added depending on the site used.

次に本発明に係るAl合金合わせ材の1つは上記Al合
金を芯材とし、その片面または両面に315wt%以上
含むろう材をクラッドするものであるが、ろう材の3i
含有量を5wt%以上と限定したのは5wt%未満では
液相線温度が高いためろう材が十分溶融せずろう付が困
難となるからである。このため通常のろう材は5〜15
wt%のSiを含有するものが使用されており、さらに
ろう付性改善の目的でBe,Si、Mg等を微量添加す
るのも良い。なおろう材は芯材の片面または両面に全肉
厚の3〜30%、より好ましくは5〜15%の範囲でク
ラッドするのが良い。またこのような合わせ材は必要に
応じて多層にクラッドする場合があるが、その場合に本
発明合金と該ろう材とは互いに接している必要はなくそ
れらの間に1層もしくは複数層の合金層を介してクラッ
ドしても良い。
Next, one of the Al alloy composite materials according to the present invention uses the above-mentioned Al alloy as a core material, and one or both sides of the core material is clad with a brazing material containing 315 wt% or more.
The reason why the content is limited to 5 wt% or more is because if it is less than 5 wt%, the liquidus temperature will be high and the brazing material will not melt sufficiently, making brazing difficult. For this reason, normal brazing filler metal is 5 to 15
Those containing wt% Si are used, and it is also good to add small amounts of Be, Si, Mg, etc. for the purpose of improving brazing properties. The brazing material is preferably clad on one or both sides of the core material in an amount of 3 to 30%, more preferably 5 to 15%, of the total thickness. In addition, such a composite material may be clad in multiple layers as necessary, but in that case, the alloy of the present invention and the brazing material do not need to be in contact with each other, and there may be one or more layers of the alloy between them. It may be clad through layers.

さらに本発明に係るAl合金合わせ材の伯の1つは上記
Al合金を芯材とし、その片面または両面に芯材より5
0mV以上卑な電位を有するA、1層合金をクラッドす
るものであるが該Al合金の電位を卑とするのはAl合
金が陰極防食における犠牲層として作用し芯材を保護す
るためであり、その電位を50m V以上としたのはこ
れ未満では十分な効果が得られないからである。
Furthermore, one of the features of the Al alloy laminated material according to the present invention is that the above-mentioned Al alloy is used as a core material, and one or both sides of the aluminum alloy have 50% of the core material.
A, which has a base potential of 0 mV or more, is used to clad a single-layer alloy, but the potential of the Al alloy is made base because the Al alloy acts as a sacrificial layer in cathodic protection and protects the core material, The reason why the potential is set to 50 mV or more is because a sufficient effect cannot be obtained if the potential is less than this.

なおこの犠牲層は全肉厚の1〜20%、より好ましくは
3〜20%の範囲でクラッドするのが良い。
Note that this sacrificial layer is preferably clad in a range of 1 to 20%, more preferably 3 to 20% of the total thickness.

またこのような合わせ材を多層にクラッドする場合は本
発明合金に係る芯材と犠牲層とは直接接している必要は
なく、犠牲層が直接接している他の芯材に対して50m
V以上卑な電位を有していれば良い。
In addition, when cladding such laminated materials in multiple layers, the core material of the alloy of the present invention and the sacrificial layer do not need to be in direct contact with each other, and the sacrificial layer is 50 m away from the other core material with which it is directly in contact.
It suffices if it has a potential that is more base than V.

以上の本発明合金および合わせ材はフラックスろう付、
不活性雰囲気ろう付および真空ろう付等いかなるろう何
丁法用材料としても使用できる。さらにこれら合金およ
び合わせ材は常法により製造することができる。
The above-mentioned alloys and composite materials of the present invention can be flux brazed,
It can be used as a material for any brazing method such as inert atmosphere brazing and vacuum brazing. Furthermore, these alloys and composite materials can be manufactured by conventional methods.

(実施例) 次に本発明を実施例により説明する。(Example) Next, the present invention will be explained by examples.

実施例(1) 第3表に示す組成のAl合金を溶解後、連続鋳造し該鋳
塊を熱間圧延した後冷間圧延と焼鈍を施して厚さ1!M
4の板材を製造した。該板材より引張り試験片を加工し
、ろう付を想定した条件として610℃の温度で5分間
加熱しその後引張り試験を行いその結果を第3表に併記
した。
Example (1) After melting an Al alloy having the composition shown in Table 3, it was continuously cast, and the ingot was hot rolled, then cold rolled and annealed to a thickness of 1! M
4 plates were manufactured. A tensile test piece was processed from the plate material, heated at a temperature of 610° C. for 5 minutes under conditions assuming brazing, and then subjected to a tensile test. The results are also listed in Table 3.

さらにろう付性の試験として第1図に示すように上記板
材の表面にプレージングシートとして第2表に示すB^
12PCを突き当てた逆Tll1手試験片を用い前処理
後フルオロアルミン酸カリウム塩からなるフラックスの
5%!!!濁液を塗布し乾燥後N2ガス雰囲気中でろう
付加熱をして突き当て部にフィレットを形成させ、その
結果を良好なフィレットが形成されたものには○印、フ
ィレットが形成されないものあるいは不均一なフィレッ
トのものにはX印として第3表に併記した。また従来合
金としてJIS 3003. JIS 3004及びJ
IS 6061について同様な試験を行ないその結果を
第3表に併記した。
Furthermore, as a brazeability test, as shown in Figure 1, a plating sheet was applied to the surface of the plate material as shown in Table 2.
5% of the flux consisting of potassium fluoroaluminate salt after pretreatment using an inverted Tll1 hand specimen against which 12 PCs were abutted! ! ! After applying the cloudy liquid and drying it, heat is added to the brazing in an N2 gas atmosphere to form a fillet at the abutting part.The results are marked with a circle if a good fillet is formed, and if a fillet is not formed or defective. Those with uniform fillets are also marked with an X in Table 3. Also, as a conventional alloy, JIS 3003. JIS 3004 and J
A similar test was conducted on IS 6061 and the results are also listed in Table 3.

第3表から明らかなように本発明合金はいずれも引張り
強さは20.4Ky f /−以上を有し従来合金より
も優れ、ろう付性も良好である。一方M9含有母が’t
wt%を超える比較合金Nα8は引張り強さは優れてい
るがろう付性が劣り、CUを含有しない比較合金Nα7
.N+を含有しない比較合金Nα9はいずれも引張り強
さが劣っている。また従来のJIS 3003合金はろ
う付性は良好であるが引張り強さが小さく、JIS 3
004合金及びJIS 6061合金はろう付性、引張
り強さともに劣っていることが判る。
As is clear from Table 3, all of the alloys of the present invention have a tensile strength of 20.4 Ky f /- or more, which is superior to conventional alloys, and also has good brazing properties. On the other hand, M9-containing mother is 't
Comparative alloy Nα8 containing more than CU has excellent tensile strength but poor brazing properties, whereas comparative alloy Nα7 containing no CU
.. All comparative alloys Nα9 containing no N+ have inferior tensile strength. In addition, conventional JIS 3003 alloy has good brazing properties but low tensile strength,
It can be seen that the 004 alloy and the JIS 6061 alloy are inferior in both brazeability and tensile strength.

実施例(2) 第3表に示す本発明合金Nα3の鋳塊を用い、この板材
を芯材とし第4表に示すようにその片面に第1表に示す
JIS 4045合金板材をろう材として全板厚の10
%の厚さでクラッドし、かつ他面にJIS 7072合
金を犠牲層の皮材として全板厚の10%の厚さでクラッ
ドした厚6i、o、の合わせ材を常法により製造した。
Example (2) Using an ingot of the alloy Nα3 of the present invention shown in Table 3, this plate was used as a core material, and as shown in Table 4, a JIS 4045 alloy plate shown in Table 1 was used as a brazing material on one side. 10 plate thickness
A laminated material having a thickness of 6i or 6o was manufactured by a conventional method, and the other side was clad with a JIS 7072 alloy to a thickness of 10% of the total plate thickness as a sacrificial layer skin material.

該合わせ材から32sX200mの板を切り出した後J
IS 5号引張り試験片に加工し、引張り試験を行ない
その結果を第4表に示した。また上記合わせ材から50
aX100#Imの板を切り出した後、JIS 404
5合金面をシールし、JIS 7072合金面からの耐
食性を評価するために500時間のCASS試験を実施
して孔食深さを測定し、その結果を第4表に示した。
After cutting out a board of 32s x 200m from the laminated material J
It was processed into an IS No. 5 tensile test piece and subjected to a tensile test, and the results are shown in Table 4. Also, from the above laminated material, 50
After cutting out the board of aX100#Im, JIS 404
5 alloy surface was sealed, and in order to evaluate the corrosion resistance from the JIS 7072 alloy surface, a 500 hour CASS test was conducted to measure the depth of pitting corrosion, and the results are shown in Table 4.

ざら(第2図に示すように上記合わせ材を第1表に示す
JIS 1050合金板材の表面に突き当てた逆T継手
試験片を用い前処理後フルオロアルミン酸カリウム塩か
らなるフラックスの懸濁液を塗布し乾燥後N2ガス雰囲
気中で600℃で5分間ろう付加熱を行ないフィレット
の形状にてろう付性を評価しその結果を第4表に示した
。また比較のため従来合金であるJIS 3003合金
を芯材とし片面にJIS 4045合金をろう材として
全板厚の10%の厚さでクラッドし、他面にJIS 7
072合金を犠牲層の皮材として全板厚の10%の厚さ
でクラッドした厚さ1.Ormの合わせ材を常法により
製造し、上記と同様な試験を行ないそれらの結果を第4
表に併記した。
After pretreatment using an inverted T-joint test piece in which the above-mentioned composite material was pressed against the surface of the JIS 1050 alloy plate material shown in Table 1 as shown in Figure 2, a suspension of flux consisting of potassium fluoroaluminate salt was applied. After coating and drying, brazing heat was applied at 600℃ for 5 minutes in an N2 gas atmosphere, and the brazing properties were evaluated based on the shape of the fillet.The results are shown in Table 4.For comparison, conventional alloy JIS 3003 alloy as a core material, one side is clad with JIS 4045 alloy as a brazing material with a thickness of 10% of the total plate thickness, and the other side is JIS 7
Thickness 1.072 alloy is used as a sacrificial skin material and is clad with a thickness of 10% of the total plate thickness. Orm laminated material was manufactured using a conventional method, and the same tests as above were conducted, and the results were summarized in the 4th section.
Also listed in the table.

なお第4表中の電位は上記合わせ材の芯材とJIS 7
072合金皮材について飽和カロメル電極を基準として
5%NaC1水溶液中で25℃の条件にて測定した値を
示す。
Note that the potentials in Table 4 are based on the core material of the above laminated material and JIS 7.
The values are shown for the 072 alloy skin material measured at 25° C. in a 5% NaCl aqueous solution using a saturated calomel electrode as a reference.

第4表から明らかなように本発明合わせ材は比較材に比
べて特に強度において優れ、かつ耐食性も勝っているこ
とが判る。
As is clear from Table 4, the laminated materials of the present invention are particularly superior in strength and corrosion resistance compared to the comparative materials.

(発明の効果〕 このように本発明によれば高い強度と優れたろう付性及
び耐食性を有する熱交換器部材を得ることができる。
(Effects of the Invention) As described above, according to the present invention, a heat exchanger member having high strength, excellent brazing properties, and corrosion resistance can be obtained.

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

第1図は本発明合金のろう付性試験を示す側面図、第2
図は本発明合わせ材のろう付性試験を示す側面図である
。 1・・・・・・・・JIS BAl2PCプレージング
シート2・・・・・・・・本発明合金 3・・・・・・・・本発明合わせ材 4・・・・・・・・JIS 1050合金板材第1図 
  第2図
Figure 1 is a side view showing the brazeability test of the alloy of the present invention, Figure 2
The figure is a side view showing a brazeability test of the laminated material of the present invention. 1...JIS BAl2PC plating sheet 2... Alloy of the present invention 3... Laminated material of the present invention 4...JIS 1050 Alloy plate material Figure 1
Figure 2

Claims (3)

【特許請求の範囲】[Claims] (1) Mg0.01〜1wt%,Si0.01〜1.
5wt%,Fe0.01〜1.0wt%,Cu0.05
〜2wt%,Ni0.6〜5wt%を含み、さらにMn
0.01〜2wt%,Cr0.001〜0.5wt%,
Zr0.001〜0.5wt%,Hf0.001〜1.
5wt%,Ti0.001〜0.5wt%,B0.00
01〜0.1wt%とZn0.5〜5wt%,In0.
005〜0.5wt%,Sn0.005〜0.5wt%
のいずれか一方または両方の群よりそれぞれ1種もしく
は2種以上の元素を含み、残部Alと不可避的不純物か
らなることを特徴とする熱交換器部材用アルミニウム合
金。
(1) Mg0.01-1wt%, Si0.01-1.
5wt%, Fe0.01-1.0wt%, Cu0.05
~2wt%, Ni0.6~5wt%, and further Mn
0.01-2wt%, Cr0.001-0.5wt%,
Zr0.001-0.5wt%, Hf0.001-1.
5wt%, Ti0.001-0.5wt%, B0.00
01-0.1wt%, Zn0.5-5wt%, In0.
005~0.5wt%, Sn0.005~0.5wt%
An aluminum alloy for heat exchanger members, characterized in that it contains one or more elements from either one or both groups, and the remainder consists of Al and unavoidable impurities.
(2) Mg0.01〜1wt%,Si0.01〜1.
5wt%,Fe0.01〜1.0wt%,Cu0.05
〜2wt%,Ni0.6〜5wt%を含み、さらにMn
0.01〜2wt%,Cr0.001〜0.5wt%,
Zr0.001〜0.5wt%,Hf0.001〜1.
5wt%,Ti0.001〜0.5wt%,B0.00
01〜0.1wt%とZn0.5〜5wt%,In0.
005〜0.5wt%,Sn0.005〜0.5wt%
のいずれか一方または両方の群よりそれぞれ1種もしく
は2種以上の元素を含み、残部Alと不可避的不純物か
らなるアルミニウム合金を芯材とし、該芯材の片面また
は両面にSi5wt%以上含むアルミニウム合金ろう材
をクラツドすることを特徴とする熱交換器部材用アルミ
ニウム合金合わせ材。
(2) Mg0.01-1wt%, Si0.01-1.
5wt%, Fe0.01-1.0wt%, Cu0.05
~2wt%, Ni0.6~5wt%, and further Mn
0.01-2wt%, Cr0.001-0.5wt%,
Zr0.001-0.5wt%, Hf0.001-1.
5wt%, Ti0.001-0.5wt%, B0.00
01-0.1wt%, Zn0.5-5wt%, In0.
005~0.5wt%, Sn0.005~0.5wt%
An aluminum alloy containing one or more elements from either or both groups, the remainder being Al and unavoidable impurities as a core material, and containing 5wt% or more of Si on one or both sides of the core material. An aluminum alloy laminated material for heat exchanger parts, characterized by cladding with brazing filler metal.
(3) Mg0.01〜1wt%,Si0.01〜1.
5wt%,Fe0.01〜1.0wt%,Cu0.05
〜2wt%,Ni0.6〜5wt%を含み、さらにMn
0.01〜2wt%,Cr0.001〜0.5wt%,
Zr0.001〜0.5wt%,Hf0.001〜1.
5wt%,Ti0.001〜0.5wt%,B0.00
01〜0.1wt%とZn0.5〜5wt%,In0.
005〜0.5wt%,Sn0.005〜0.5wt%
のいずれか一方または両方の群よりそれぞれ1種もしく
は2種以上の元素を含み、残部Alと不可避的不純物か
らなるアルミニウム合金を芯材とし、該芯材の片面また
は両面に芯材よりも50mV以上卑な電位を有するアル
ミニウム合金をクラツドすることを特徴とする熱交換器
部材用アルミニウム合金合わせ材。
(3) Mg0.01-1wt%, Si0.01-1.
5wt%, Fe0.01-1.0wt%, Cu0.05
~2wt%, Ni0.6~5wt%, and further Mn
0.01-2wt%, Cr0.001-0.5wt%,
Zr0.001-0.5wt%, Hf0.001-1.
5wt%, Ti0.001-0.5wt%, B0.00
01-0.1wt%, Zn0.5-5wt%, In0.
005~0.5wt%, Sn0.005~0.5wt%
The core material is an aluminum alloy containing one or more elements from either one or both groups, the remainder being Al and unavoidable impurities, and one or both sides of the core material has a voltage of 50 mV or more than the core material. An aluminum alloy laminated material for a heat exchanger member, characterized in that it is clad with an aluminum alloy having a base potential.
JP13077087A 1987-05-27 1987-05-27 Aluminum alloy and aluminum alloy clad material for heat exchanger member Pending JPS63293136A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP13077087A JPS63293136A (en) 1987-05-27 1987-05-27 Aluminum alloy and aluminum alloy clad material for heat exchanger member

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP13077087A JPS63293136A (en) 1987-05-27 1987-05-27 Aluminum alloy and aluminum alloy clad material for heat exchanger member

Publications (1)

Publication Number Publication Date
JPS63293136A true JPS63293136A (en) 1988-11-30

Family

ID=15042249

Family Applications (1)

Application Number Title Priority Date Filing Date
JP13077087A Pending JPS63293136A (en) 1987-05-27 1987-05-27 Aluminum alloy and aluminum alloy clad material for heat exchanger member

Country Status (1)

Country Link
JP (1) JPS63293136A (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH0394037A (en) * 1989-09-05 1991-04-18 Furukawa Alum Co Ltd Aluminum alloy fin material for vapor phase brazing
EP0793734A1 (en) * 1994-10-27 1997-09-10 Reynolds Metals Company Machineable aluminum alloys containing in and sn and process for producing the same
JP2010242112A (en) * 2009-03-31 2010-10-28 Kobe Steel Ltd High-strength aluminum alloy brazing sheet

Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS59100251A (en) * 1982-11-30 1984-06-09 Kobe Steel Ltd Corrosion resistant aluminum alloy with high strength for brazing

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS59100251A (en) * 1982-11-30 1984-06-09 Kobe Steel Ltd Corrosion resistant aluminum alloy with high strength for brazing

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH0394037A (en) * 1989-09-05 1991-04-18 Furukawa Alum Co Ltd Aluminum alloy fin material for vapor phase brazing
EP0793734A1 (en) * 1994-10-27 1997-09-10 Reynolds Metals Company Machineable aluminum alloys containing in and sn and process for producing the same
EP0793734A4 (en) * 1994-10-27 1998-02-25 Reynolds Metals Co Machineable aluminum alloys containing in and sn and process for producing the same
JP2010242112A (en) * 2009-03-31 2010-10-28 Kobe Steel Ltd High-strength aluminum alloy brazing sheet

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