JPS6032703B2 - Al material for brazing - Google Patents

Al material for brazing

Info

Publication number
JPS6032703B2
JPS6032703B2 JP53136119A JP13611978A JPS6032703B2 JP S6032703 B2 JPS6032703 B2 JP S6032703B2 JP 53136119 A JP53136119 A JP 53136119A JP 13611978 A JP13611978 A JP 13611978A JP S6032703 B2 JPS6032703 B2 JP S6032703B2
Authority
JP
Japan
Prior art keywords
brazing
corrosion
strength
amount
present
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.)
Expired
Application number
JP53136119A
Other languages
Japanese (ja)
Other versions
JPS5562140A (en
Inventor
弥五郎 広瀬
昌治 海部
純由 平井
日出男 藤本
淳 瀧川
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.)
Kobe Steel Ltd
Original Assignee
Kobe Steel 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 Kobe Steel Ltd filed Critical Kobe Steel Ltd
Priority to JP53136119A priority Critical patent/JPS6032703B2/en
Publication of JPS5562140A publication Critical patent/JPS5562140A/en
Publication of JPS6032703B2 publication Critical patent/JPS6032703B2/en
Expired legal-status Critical Current

Links

Classifications

    • BPERFORMING OPERATIONS; TRANSPORTING
    • B23MACHINE TOOLS; METAL-WORKING NOT OTHERWISE PROVIDED FOR
    • B23KSOLDERING OR UNSOLDERING; WELDING; CLADDING OR PLATING BY SOLDERING OR WELDING; CUTTING BY APPLYING HEAT LOCALLY, e.g. FLAME CUTTING; WORKING BY LASER BEAM
    • B23K35/00Rods, electrodes, materials, or media, for use in soldering, welding, or cutting
    • B23K35/22Rods, electrodes, materials, or media, for use in soldering, welding, or cutting characterised by the composition or nature of the material
    • B23K35/24Selection of soldering or welding materials proper
    • B23K35/28Selection of soldering or welding materials proper with the principal constituent melting at less than 950 degrees C
    • B23K35/286Al as the principal constituent

Description

【発明の詳細な説明】 本発明は高温強度を保持し且つ耐食性の改善されたろう
付用の山材料に関するものである。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a pile material for brazing that maintains high temperature strength and has improved corrosion resistance.

AIは一般に耐食性の良好な材料として知られているが
、例えば熱交換器の様なろう付構造体として使用する場
合は、ろう材中のSiが山母材中に拡散し、該Sjを核
として周囲の山母村との間の局部電池が形成される結果
、粒界腐食を起こすという危険がある。そこでこの様な
腐食を防止する方法として以下の如き方法が提案されて
いるけれども、いずれも現実的な方策とは言い難い面が
ある。以下公知方法を概説する。○} 陽極的に作用す
る元素(ZnやSn等)を利用する方法(1‐i)ろう
材や芯材に形成されるクラッドの表面に、ZnやSn等
の添加された材料を更にクラツドする方法(1‐U)ろ
う材中にZnやSn等を添加してろう材自体を陽極的に
作用する様に改資する方法(1‐並)熱交換器における
フィン材の如く、装置の.一部に、ZnやSn等の添加
された材料を使用し、その陽極的作用によって他の構成
部分を保護する方法‘21 Siに対するN母材の耐粒
界拡散性を改善強化する方法湖 母材中に第3成分を添
加して母材をろう材との対比において陰極的に作用する
様に改賞する方法。
AI is generally known as a material with good corrosion resistance, but when used as a brazed structure such as a heat exchanger, the Si in the brazing filler metal diffuses into the base metal, causing the Sj to become a core. There is a risk that intergranular corrosion may occur as a result of the formation of a local battery between the surrounding mountain village and the surrounding area. Therefore, although the following methods have been proposed as methods for preventing such corrosion, it is difficult to say that any of them are realistic measures. The known methods will be outlined below. ○} Method using elements that act as an anode (Zn, Sn, etc.) (1-i) Further cladding the surface of the cladding formed on the brazing material or core material with added materials such as Zn or Sn. Method (1-U) A method in which Zn, Sn, etc. are added to the brazing filler metal so that the brazing filler metal itself acts as an anode (1-Normal) A method for adding Zn, Sn, etc. to the brazing filler metal so that it acts as an anode (1-Normal) A method of using a material added with Zn, Sn, etc. in a part and protecting other components by its anodic action '21 A method of improving and strengthening the grain boundary diffusion resistance of the N base material against Si A method in which a third component is added to the material to modify the base material so that it acts cathodically in comparison to the brazing material.

ところが(1−i)の方法では製造条件が複雑になって
生産コストが高騰するという欠点がある。
However, method (1-i) has the disadvantage that manufacturing conditions become complicated and production costs rise.

又(1一U)のうちZnを利用する方法は、耐食性改善
効果が顕著であるにもかかわらず、Znの蒸気圧が高い
為にろう付時に蒸発飛散して炉の汚染を招くという問題
がある。そしてZnの代りにSnを利用する方法では、
蒸発飛散という問題を回避することができた代りに加工
性が低くなるという欠点があり、圧延の実施が困難であ
るから実用性がない。更に(1−餌)の方法では、例え
ばへツダータンクの様にフィン材と直接接触しない部材
については保護が及ばないため極めて不完全な方法と言
わなければならない。又■及び【3iの改善強化法とし
て、例えばプレージングシート芯材用材料として汎用さ
れているN材料(例えばJIS3003材)にCu、F
e、Cr、Z首等を添加したり、或はソーキング等の熱
処理条件を変更したりする試みがなされているが、未だ
満足すべき成果は得られていない。尚この3003材は
、Mhを主要成分の1つとするもので、周知の如く耐食
性自体は極めて良好であるが、ろう付条件下(即ち高温
加熱下)では粒界腐食の感受性が極めて高いものとなり
、なんらかの改質が望まれている。また他方では上記3
003材や3203材の如きAI−Nh系合金〔Mn:
1.0〜1.5%(以下%は重量%を意味する)〕が高
温強度において劣ることに着目し、Mnの含有量を特定
(0.5〜1.5%)しつつCr、Ti、Zrを配合す
ることによって加工性及び高温強度の両特性を満足する
ろう付け用アルミニウム合金を提供しようとする試みも
ある(特関昭50−118919)。
Furthermore, although the method of using Zn among (11U) has a remarkable effect of improving corrosion resistance, due to the high vapor pressure of Zn, it evaporates and scatters during brazing, causing contamination of the furnace. be. And in the method of using Sn instead of Zn,
Although the problem of evaporation and scattering can be avoided, it has the disadvantage that workability is reduced, and rolling is difficult, so it is not practical. Furthermore, the method (1-bait) cannot protect members that do not come into direct contact with the fin material, such as a hetuda tank, so it must be said that it is an extremely incomplete method. In addition, as an improvement and strengthening method for ■ and [3i, for example, Cu, F
Attempts have been made to add E, Cr, Z neck, etc., or to change heat treatment conditions such as soaking, but no satisfactory results have been obtained yet. This 3003 material has Mh as one of its main components, and as is well known, it has extremely good corrosion resistance, but under brazing conditions (i.e., under high temperature heating), it becomes extremely susceptible to intergranular corrosion. , some kind of modification is desired. On the other hand, the above 3
AI-Nh alloys such as 003 material and 3203 material [Mn:
1.0 to 1.5% (hereinafter % means weight %)] is inferior in high temperature strength, and while specifying the Mn content (0.5 to 1.5%), Cr, Ti There has also been an attempt to provide an aluminum alloy for brazing that satisfies both the properties of workability and high-temperature strength by blending Zr into the aluminum alloy (Tokukan Sho 50-118919).

但し同公報には、Mn量を少なくし過ぎると十分な強度
を与えることができないと述べられており、後述する如
くこの記載は本発明者等の知見と一致するものではなも
、。又同公報にはMn量を過大(1.5%以上)にする
と巨大なA1一Mn化合物が形成されて加工性が低下す
る旨も記載されているがMn過剰と粒界腐食感受性の関
係については述べられていない。本発明はこの様な情況
下になされたものであって、ろう材成分時にSiの母材
中での拡散性が抑制されると共に、高強度特性を犠牲に
しないでそれ自体の粒界腐食感受性が低いろう付用AI
材料を提供することを目的とする。
However, the publication states that if the amount of Mn is too small, sufficient strength cannot be provided, and as will be described later, this statement does not match the findings of the present inventors. The same publication also states that if the amount of Mn is excessive (1.5% or more), a huge A1-Mn compound is formed and the workability deteriorates, but regarding the relationship between excessive Mn and intergranular corrosion susceptibility is not mentioned. The present invention has been made under these circumstances, and it is possible to suppress the diffusivity of Si in the base metal when forming a brazing filler metal, and to reduce its own intergranular corrosion susceptibility without sacrificing high strength properties. AI for brazing with low
The purpose is to provide materials.

そして本発明に係る該材料とは、Mnを0.003〜0
.3%、Cuを0.003〜0.5%の範囲で必須的に
含むと共に、Zr、Cr及びTiのうち少なくとも1種
を0.05〜0.3%、残り2種を0.3%以下含み、
且つ残部がAI及び不可避的不純物からなるものである
点に要旨が存在する。即ちMnの配合量を高強度特性が
失なわれない範囲で低く押えることによって粒界腐食感
受性を低いものとし、且つZr、Cr、Tiの少なくと
も1種を所定範囲内の量加えることによって耐拡散性の
向上を画っている。次にこれら各成分配合量の限定理由
を述べる。
The material according to the present invention has Mn of 0.003 to 0.
.. 3%, Cu in the range of 0.003 to 0.5%, and at least one of Zr, Cr, and Ti at 0.05 to 0.3%, and the remaining two at 0.3%. Including the following,
The gist is that the remainder consists of AI and unavoidable impurities. In other words, susceptibility to intergranular corrosion is lowered by keeping the amount of Mn blended as low as possible without losing high strength properties, and diffusion resistance is achieved by adding at least one of Zr, Cr, and Ti in an amount within a predetermined range. It depicts sexual improvement. Next, the reason for limiting the blending amount of each of these components will be described.

まずNhであるが、Mn量が増大する母材としての強度
は向上するが、同時に粒界腐食感受性も高まってくるの
で、種々研究しこれら両性質を同時に満足できる最大量
は0.3%であることを見出した。但し0.003%以
上を確保しなければ高温強度を十分に発揮させることが
できなくなる。即ち0.3%以下のMn量であっても、
従来の知見と異なって高温強度の低下を招かないことが
見出された。次にCuは結晶粒の微細化及び強度向上の
両効果を有するが、0.5%を超えると却って耐食性の
劣化がみられるので、0.5%を上限と定めた。但し0
.003%禾満になると結晶粒の微細化並びに強度向上
の両効果が発揮されなくなる。最後にZr、Cr及びT
iの3元素であるが、これら1種でも耐拡散性の改良及
び強度の向上機能を発揮する。しかしこれらの配合量が
3種とも0.05%未満では前記効果は享受できず、少
なくとも1種は0.05%以上なければならない。逆に
3種とも0.3%を超えると加工性低下という問題が生
じる。次に本発明を実施例によって更に具体的に述べる
。尚下記の例はプレージングシート用芯材として利用す
る場合を述べるものであるが、フィン材、その他各種の
単体構成部品としても利用できることは言う迄もない。
下記組成の芯材を準備した。
First of all, regarding Nh, as the amount of Mn increases, the strength as a base material improves, but at the same time, the susceptibility to intergranular corrosion also increases, so after various researches, the maximum amount that can satisfy both of these properties at the same time is 0.3%. I discovered something. However, unless a content of 0.003% or more is ensured, high temperature strength cannot be fully exhibited. That is, even if the Mn content is 0.3% or less,
It was found that, unlike conventional knowledge, this did not cause a decrease in high temperature strength. Next, Cu has the effect of both refining crystal grains and improving strength, but if it exceeds 0.5%, corrosion resistance will deteriorate, so 0.5% is set as the upper limit. However, 0
.. When the grain density reaches 0.03%, both the effects of grain refinement and strength improvement are no longer exhibited. Finally, Zr, Cr and T
Although there are three elements i, even just one of these exhibits the function of improving diffusion resistance and strength. However, if the amount of these three types is less than 0.05%, the above effects cannot be obtained, and at least one of these types must be 0.05% or more. On the other hand, if the content of all three types exceeds 0.3%, there will be a problem of decreased workability. Next, the present invention will be described in more detail with reference to Examples. Although the following example describes a case where the material is used as a core material for a plating sheet, it goes without saying that it can also be used as a fin material and various other single component parts.
A core material having the following composition was prepared.

試料NO.1〜3は本発明芯材であり、試料No.4〜
6は比較芯材である。第 1 表 (注:残部はAI及び不可避的不純物:※)この芯材に
対し、第2表に示す組成のろう材を夫々15%ずつ両面
にクラッドし、板厚0.6帆のプレージングシートを作
成した。
Sample No. 1 to 3 are the core materials of the present invention, and sample No. 3 is the core material of the present invention. 4~
6 is a comparative core material. Table 1 (Note: The remainder is AI and unavoidable impurities: *) This core material was clad with 15% brazing filler metal of the composition shown in Table 2 on both sides, and plated with a board thickness of 0.6 sail. I created a sheet.

第2表 この板の中央部に、JIS・Z−2247(ヱーJクセ
ン試験法)に準じたェリクセン加工を施こし、深さ8側
の凹部を形成した。
Table 2 The central part of this plate was subjected to Eriksen processing in accordance with JIS Z-2247 (E-J Kusen Test Method) to form a recess on the depth 8 side.

これをN2ガス雰囲気(露点:−60oo以下)中で6
05q○、2分間の加熱を行なって試験片とし、この試
験片をアノード電解促進試験法によって腐食試験を行な
った。尚試験片裏側の凹部に対応する最突出先端部を電
極に向わせる様にセットした。腐食液:0.州aCI水
溶液 試験電流:0.2mA/の、16時間 前記凹部の縦断面をケーラー(Keller)氏液でエ
ッチングしたものについてその顕微鏡写真(Ion音)
を第1〜6図として示す。
6 in a N2 gas atmosphere (dew point: -60oo or less)
05q○ was heated for 2 minutes to obtain a test piece, and this test piece was subjected to a corrosion test using an accelerated anodic electrolysis test method. The test piece was set so that the most protruding tip corresponding to the recess on the back side faced the electrode. Corrosive liquid: 0. State aCI aqueous solution test current: 0.2 mA/, 16 hours Micrograph of the vertical cross section of the recess etched with Keller's solution (Ion sound)
are shown in Figures 1-6.

第1〜6図は前記試料片番号1〜6に対応するが、第4
〜6図では粒界に沿って相当の腐食が見られるのに対し
、第1〜3図ではほとんど腐食がみられず、耐粒界腐食
性の優れていることがわかる。尚第4,5図ではMnが
過剰量配合されているため比較的密な粒界に沿って分散
する様な腐食進行が見られるのに対し、第6図ではCu
が過剰量配合されているため粗な粒界に沿って腐食が進
行し、又進行深さも大きく、Cuが過剰量になると却っ
て耐食性が劣化することがわかる。一方本発明では前記
した様に高温強度の保持が重要な課題の1つとなってい
るので、第3表に示す如くMn含有量が本発明の条件を
満足するもの(試料No.7〜16)と従来の300針
材や3203材の様にMn含有量が多いもの(試料No
.17〜19)を比較し、次の様な実験を行なった。
1 to 6 correspond to the sample pieces numbers 1 to 6, but the fourth
Although considerable corrosion is seen along the grain boundaries in Figures 1 to 6, almost no corrosion is seen in Figures 1 to 3, indicating that the grain boundary corrosion resistance is excellent. In Figures 4 and 5, Mn is blended in an excessive amount, so corrosion progresses as if it is dispersed along relatively dense grain boundaries, whereas in Figure 6, Cu
Since Cu is blended in an excessive amount, corrosion progresses along coarse grain boundaries, and the depth of corrosion is also large, indicating that an excessive amount of Cu actually deteriorates corrosion resistance. On the other hand, in the present invention, as mentioned above, maintaining high temperature strength is one of the important issues, so as shown in Table 3, the Mn content satisfies the conditions of the present invention (Samples No. 7 to 16). and conventional 300 needle material and 3203 material with high Mn content (sample No.
.. 17 to 19) and conducted the following experiments.

即ち第3表に示す成分からなる芯材オに対し、第2表に
示した組成のろう材を夫々15%ずつ両面にクラッドし
、板厚0.6凧のプレージングシートを作成した。これ
をろう付温度直下の550℃で10分間加熱した後、室
温まで冷却し引張試験を行なったところ、第3表に併記
する様な結果が得られた。同表に示される様にMh量を
従来のJIS規格より少なくした試料(No.7〜16
)であっても、高温強度は犠牲にされておらず、高温強
度を保持しつつ耐食性を向上させるという本発明の目的
が十分に達成されたことを知ることができる。第3表 (洋:残部N及び不可避的不純物) 本発明は以上の如く構成されているので、ろう付用AI
母材としての強度を維持しつつ耐拡散性が改善され、し
かも粒界腐食感受性を十分に低く押えることに成功して
おり、ろう付釘構造体の耐腐食性が大幅に改善されるこ
とになった。
That is, a core material O consisting of the components shown in Table 3 was clad with 15% of each of the brazing filler metals having the composition shown in Table 2 on both sides to prepare a plating sheet having a thickness of 0.6. This was heated for 10 minutes at 550° C., just below the brazing temperature, and then cooled to room temperature and subjected to a tensile test, and the results shown in Table 3 were obtained. As shown in the same table, samples with a lower Mh content than the conventional JIS standard (No. 7 to 16)
), the high-temperature strength was not sacrificed, and it can be seen that the objective of the present invention of improving corrosion resistance while maintaining high-temperature strength was fully achieved. Table 3 (Western: remaining N and unavoidable impurities) Since the present invention is configured as described above, the brazing AI
Diffusion resistance has been improved while maintaining the strength of the base material, and the susceptibility to intergranular corrosion has been successfully suppressed to a sufficiently low level, resulting in a significant improvement in the corrosion resistance of brazed nail structures. became.

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

第1〜6図は図面代用顕微鏡写真(10針音)である。 灘磯鰹蝿擬灘鰯雲≦茎 麹議員鯵 灘灘藁蝿 鴎溝灘灘雪 繊麗磯 Figures 1 to 6 are microscopic photographs (10 stitches) in place of drawings. Nada bonito fly pseudo Nada sardine cloud ≦ stem Koji member horse mackerel Nada straw fly Kamomizo Nada Snow Shinreiso

Claims (1)

【特許請求の範囲】 1 Mn:0.003〜0.3%(重量%の意味、以下
同じ)Cu:0.003〜0.5% を必須成分として含む他、Cr、Zr、Tiよりなる群
から選択される少なくとも1種を0.05〜0.3%、
残り2種を0.3%以下含み、残部がAl及び不可避不
純物からなることを特徴とするろう付用Al材料。
[Claims] 1 Contains Mn: 0.003 to 0.3% (meaning by weight %, the same applies hereinafter) Cu: 0.003 to 0.5% as an essential component, and also consists of Cr, Zr, and Ti 0.05 to 0.3% of at least one selected from the group;
An Al material for brazing, characterized in that it contains 0.3% or less of the remaining two types, with the remainder consisting of Al and unavoidable impurities.
JP53136119A 1978-11-04 1978-11-04 Al material for brazing Expired JPS6032703B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP53136119A JPS6032703B2 (en) 1978-11-04 1978-11-04 Al material for brazing

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP53136119A JPS6032703B2 (en) 1978-11-04 1978-11-04 Al material for brazing

Publications (2)

Publication Number Publication Date
JPS5562140A JPS5562140A (en) 1980-05-10
JPS6032703B2 true JPS6032703B2 (en) 1985-07-30

Family

ID=15167739

Family Applications (1)

Application Number Title Priority Date Filing Date
JP53136119A Expired JPS6032703B2 (en) 1978-11-04 1978-11-04 Al material for brazing

Country Status (1)

Country Link
JP (1) JPS6032703B2 (en)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS58110653A (en) * 1981-12-23 1983-07-01 Kobe Steel Ltd Heat exchanger made of brazed aluminum
JPH0270397A (en) * 1988-09-06 1990-03-09 Kobe Steel Ltd Aluminum of aluminum alloy member for inert gaseous atmosphere brazing

Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS4842522A (en) * 1971-10-01 1973-06-20
JPS50118919A (en) * 1974-03-01 1975-09-18
US4093782A (en) * 1977-03-03 1978-06-06 Swiss Aluminium Ltd. Brazed aluminum composite
US4098957A (en) * 1977-11-25 1978-07-04 Aluminum Company Of America Aluminum brazing sheet

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS4842522A (en) * 1971-10-01 1973-06-20
JPS50118919A (en) * 1974-03-01 1975-09-18
US4093782A (en) * 1977-03-03 1978-06-06 Swiss Aluminium Ltd. Brazed aluminum composite
US4098957A (en) * 1977-11-25 1978-07-04 Aluminum Company Of America Aluminum brazing sheet

Also Published As

Publication number Publication date
JPS5562140A (en) 1980-05-10

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