JP2016179494A - Aluminum material brazing method - Google Patents

Aluminum material brazing method Download PDF

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JP2016179494A
JP2016179494A JP2015062072A JP2015062072A JP2016179494A JP 2016179494 A JP2016179494 A JP 2016179494A JP 2015062072 A JP2015062072 A JP 2015062072A JP 2015062072 A JP2015062072 A JP 2015062072A JP 2016179494 A JP2016179494 A JP 2016179494A
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brazing
aluminum
organic resin
resin
aluminum alloy
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JP6470603B2 (en
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三宅 秀幸
Hideyuki Miyake
秀幸 三宅
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MA Aluminum Corp
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Mitsubishi Aluminum Co Ltd
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Abstract

PROBLEM TO BE SOLVED: To realize appropriate brazing using an Al-Si-Mg base brazing material during brazing.SOLUTION: A method of brazing aluminum materials with each other by using a cladding material obtained by bonding an Al-Si-Mg brazing material containing, by mass%, 0.2-3.0% of Mg and 3-12% of Si to an aluminum alloy core material, in which an organic resin consisting only of C, H, and O is interposed at least in a bonded portion between the Al-Si-Mg based brazing material and the aluminum bonded member before brazing, and a surface of the bonded portion is protected from the atmosphere with a carbide film obtained by the organic resin as a barrier during brazing heating.SELECTED DRAWING: Figure 1

Description

本発明は、Al−Si−Mg系ろう材を用いたアルミニウム材のろう付方法に関するものである。   The present invention relates to a method for brazing an aluminum material using an Al-Si-Mg brazing material.

自動車用熱交換器をはじめとしたろう付分野においては、現在、ノコロックフラックスを用いた工法が主流となっているが、薄肉高強度化に有効なMg添加アルミニウム合金がフラックスの不活性化反応(MgFの形成)により使用できないという問題がある。
これに対し、量産性に配慮した、大気圧下で行うフラックスレス(フラックスを使用しない)ろう付方法も提案されてきているが、特殊な表面処理や材料仕様、ろう付工法などが採用され、コスト、品質安定性に問題があり、本格的な実用化には至っていない。
これに対し、特許文献1においては、Al−Si−Mg合金ろう材を用いたフラックスレス工法が提案されている。
Currently, in the brazing field including automotive heat exchangers, the construction method using nocolok flux is the mainstream, but Mg-added aluminum alloys that are effective in increasing the thickness and strength of the flux are the flux deactivation reactions. There is a problem that it cannot be used due to (formation of MgF 2 ).
On the other hand, fluxless (no flux) brazing method has been proposed in consideration of mass productivity, but special surface treatment, material specifications, brazing method, etc. have been adopted. There are problems with cost and quality stability, and it has not yet been put into practical use.
On the other hand, in Patent Document 1, a fluxless method using an Al—Si—Mg alloy brazing material is proposed.

特許第4547032号公報Japanese Patent No. 4547032

しかし、特許文献1においても、接合部のフィレット形成能は、従来のノコロックフラックスに対し優位性を有するには至っておらず、安定した量産品質を得るには適用製品形状を限定する必要がある。このような背景により、薄肉高強度化に有効なMg添加アルミニウム合金が使用でき、かつ、従来ノコロックろう付法と同等あるいはそれ以上のフィレット形成能をもつろう付工法の開発が強く望まれている状況である。   However, even in Patent Document 1, the fillet forming ability of the joint does not have an advantage over the conventional nocolock flux, and it is necessary to limit the applied product shape in order to obtain stable mass production quality. . With such a background, it is strongly desired to develop a brazing method that can use an Mg-added aluminum alloy that is effective for increasing the thickness and strength, and that has a fillet forming ability equal to or higher than that of the conventional Nocolok brazing method. Is the situation.

本願発明は、上記事情を背景としてなされたものであり、Al−Si−Mg系ろう材を用いて良好なろう付を行うことができるアルミニウム材のろう付方法を提供することを目的とする。   The present invention has been made against the background of the above circumstances, and an object of the present invention is to provide a brazing method for an aluminum material that can be satisfactorily brazed using an Al—Si—Mg brazing material.

すなわち、本発明のアルミニウム材のろう付方法のうち、第1の形態は、質量%でMgを0.2〜3.0%、Siを3〜12%含有するAl−Si−Mg系ろう材をアルミニウム合金芯材に貼り合せたクラッド材を用いてアルミニウム材同士をろう付する方法であって、
少なくとも、前記Al−Si−Mg系ろう材とアルミニウム被接合部材との接合部において、ろう付前にC、H、Oのみからなる有機物樹脂を介在させ、ろう付加熱時に前記有機物樹脂により得られる炭化物膜で接合部表面を雰囲気からバリヤーし、酸化物を除去するためのフラックスを用いないことを特徴とする。
That is, in the brazing method for an aluminum material according to the present invention, the first embodiment is an Al—Si—Mg based brazing material containing 0.2 to 3.0% Mg and 3 to 12% Si in mass%. Is a method of brazing aluminum materials using a clad material bonded to an aluminum alloy core material,
At least at the joint between the Al—Si—Mg-based brazing material and the aluminum member to be joined, an organic resin consisting only of C, H, O is interposed before brazing, and is obtained by the organic resin at the time of brazing addition heat. It is characterized by using a carbide film to barrier the surface of the joint from the atmosphere and not using a flux for removing oxides.

他の形態のアルミニウム材のろう付方法の発明は、前記形態の本発明において、前記有機物樹脂を数平均分子量300〜60000として、0.1〜5g/mの量で前記接合部に介在させることを特徴とする。 In another aspect of the invention of the brazing method for an aluminum material, in the present invention of the above aspect, the organic resin is interposed in the joint in an amount of 0.1 to 5 g / m 2 with a number average molecular weight of 300 to 60,000. It is characterized by that.

他の形態のアルミニウム材のろう付方法の発明は、前記形態の本発明において、前記炭化物膜は、ろう付昇温過程でろう材融点に到達するまでに蒸散することを特徴とする。   Another form of the invention of the brazing method for an aluminum material is characterized in that, in the present invention of the above form, the carbide film evaporates before reaching the melting point of the brazing material in the brazing temperature rising process.

他の形態のアルミニウム材のろう付方法の発明は、前記形態の本発明において、前記有機物樹脂が、エポキシ樹脂、または、エポキシ樹脂と他の樹脂の混合物、または、エポキシ基またはエポキシ環が重合された樹脂であることを特徴とする。   In another aspect of the invention of the brazing method for an aluminum material, the organic resin is an epoxy resin, a mixture of an epoxy resin and another resin, or an epoxy group or an epoxy ring. It is characterized by being a resin.

他の形態のアルミニウム材のろう付方法の発明は、前記形態の本発明において、前記Al−Si−Mg系ろう材に、質量%で0.02〜0.3%のBiを含有することを特徴とする。   In another aspect of the invention of the brazing method for an aluminum material, in the present invention of the above form, the Al-Si-Mg-based brazing material contains 0.02 to 0.3% Bi in mass%. Features.

次に、本願発明で規定する内容について説明する。なお、成分量はいずれも質量%で示される。   Next, the contents defined in the present invention will be described. In addition, all component amounts are shown in mass%.

<ろう材>
Si:3〜12%
Siは、Alに含有することにより、その融点を低下させ、ろう付昇温時の共晶温度以上で、接合に必要な溶融ろう材を生成する。また、ろう材表面に存在するSi粒子上では、アルミニウムの緻密な酸化皮膜の成長が抑制され、酸化皮膜の欠陥部が生成する。Siの含有量が3%未満では、これらの作用が十分に得られず、12%を超えると、ろう材強度が高くなり過ぎて圧延性が悪化し、クラッド圧延材を作製することができなくなる。このため、Siの含有量は、3〜12%とすることが好ましい。なお、同様の理由により、Siの含有量は、下限を5.0%、上限を11.0%とすることがより好ましい。
<Brazing material>
Si: 3 to 12%
When Si is contained in Al, its melting point is lowered, and a molten brazing material necessary for joining is generated at a temperature equal to or higher than the eutectic temperature at the time of brazing temperature rise. Further, on the Si particles existing on the surface of the brazing material, the growth of a dense oxide film of aluminum is suppressed, and a defective portion of the oxide film is generated. If the Si content is less than 3%, these effects cannot be obtained sufficiently. If the Si content exceeds 12%, the brazing filler metal strength becomes too high and the rollability deteriorates, making it impossible to produce a clad rolled material. . For this reason, it is preferable that content of Si shall be 3 to 12%. For the same reason, the Si content is more preferably set to a lower limit of 5.0% and an upper limit of 11.0%.

Mg:0.2〜3.0%
Mgは、ろう付昇温過程において、材料表面に生成する緻密な酸化皮膜(A1膜)に作用して酸化皮膜を分解することで、ろうの濡れ性や流動性を向上させる。ただし、Mgの含有量が0.2%未満では、酸化皮膜の分解作用が十分に得られず、3.0%を超えると、ろう材強度が高くなり過ぎて圧延性が悪化し、クラッド圧延材を作製することが難しくなる。また、MgOが厚く成長し酸化皮膜の分解作用が低下するため、溶融ろうの濡れ性が低下し、十分な接合が得られ難くなる。このため、Mgの含有量は、0.2〜3.0%とすることが好ましい。なお、同様の理由により、Mgの含有量は、下限を0.25%、上限を2.0%とすることがより好ましい。
Mg: 0.2-3.0%
Mg acts on a dense oxide film (A1 2 O 3 film) generated on the surface of the material in the brazing temperature rising process to decompose the oxide film, thereby improving the wettability and fluidity of the brazing. However, if the Mg content is less than 0.2%, the oxide film cannot be sufficiently decomposed. If it exceeds 3.0%, the brazing filler metal strength becomes too high and the rollability deteriorates, and the clad rolling It becomes difficult to produce the material. Further, since MgO grows thick and the decomposition action of the oxide film is lowered, the wettability of the molten braze is lowered, and it becomes difficult to obtain sufficient bonding. For this reason, the content of Mg is preferably 0.2 to 3.0%. For the same reason, the Mg content is more preferably 0.25% for the lower limit and 2.0% for the upper limit.

Bi:0.02〜0.3%
Biは、Mgと共存することで融点が低下し、低い温度からろうの染み出しが発生し、この部位を起点に酸化皮膜の破壊や分断が進み、溶融ろうの濡れ性が向上し、より安定した接合状態を得ることが可能となるため所望により含有させる。上記作用を得るためには0.02%以上の含有が望ましく、0.02%未満の含有では効果が不十分となる。一方、0.3%を超えて含有すると、ろう材の圧延性低下を招く。これらのためBiの含有量は上記範囲が望ましい。なお、同様の理由で下限を0.05%、上限を0.2%とするのが一層望ましい。
Bi: 0.02-0.3%
Bi has a lower melting point due to coexistence with Mg, and exudation of wax occurs from a low temperature. Oxide film breaks up and breaks away from this site, improving the wettability of the molten wax and making it more stable. Since it becomes possible to obtain the joined state, it is contained if desired. In order to acquire the said effect | action, content of 0.02% or more is desirable, and an effect will become inadequate if it contains less than 0.02%. On the other hand, when it contains exceeding 0.3%, the rolling property of a brazing material will fall. For these reasons, the Bi content is preferably within the above range. For the same reason, it is more desirable to set the lower limit to 0.05% and the upper limit to 0.2%.

<有機物樹脂種別>
有機物樹脂は、C、H、Oのみからなり、ろう付け加熱に際し炭化物膜を形成し、アルミニウム材やろう材表面の酸化皮膜成長を阻害することができる。本発明としては、有機物樹脂の種別などが限定されるものではなく、目的を達成できるものであればよい。例えば、エポキシ樹脂、または、エポキシ樹脂と他の樹脂の混合物、または、エポキシ基またはエポキシ環が重合された樹脂が例示される。エポキシ系樹脂を使用することで塗装性や経済性に優れる。
<有機物樹脂分子量>
有機物分子量は本発明としては限定されるものではないが、数平均分子量が300〜60000とするのが望ましい。
数平均分子量が300未満では、ろう付昇温過程で早期に分解蒸発して酸化皮膜成長抑制作用が不十分となり、数平均分子量が60000超となると、ろう材溶融後に残渣が生じるため溶融ろうの濡れ拡がり性を阻害する。
下限を1000、上限を10000とするのが一層望ましい。
<有機物樹脂介在量>
有機物樹脂介在量は、本発明としては特に限定されるものではないが、0.1g/m〜5g/mの範囲が望ましい。介在量が0.1g/mであると、ろう付昇温過程で早期に分解消失して酸化皮膜成長抑制作用が不十分となり、5g/m以上ではろう材溶融後に残渣が生じるため溶融ろうの濡れ拡がり性を阻害する。
同様の理由で下限を0.2g/m、上限を3.0g/mとするのが一層望ましい。
<Organic resin type>
The organic resin is composed only of C, H, and O, can form a carbide film during brazing heating, and can inhibit the growth of an oxide film on the surface of the aluminum material or the brazing material. In the present invention, the type of the organic resin is not limited, and any organic resin may be used as long as the object can be achieved. For example, an epoxy resin, a mixture of an epoxy resin and another resin, or a resin in which an epoxy group or an epoxy ring is polymerized is exemplified. Excellent paintability and economy by using epoxy resin.
<Molecular resin molecular weight>
The organic molecular weight is not limited in the present invention, but the number average molecular weight is preferably 300 to 60000.
If the number average molecular weight is less than 300, it decomposes and evaporates early in the brazing temperature rising process and the oxide film growth inhibiting action becomes insufficient. If the number average molecular weight exceeds 60,000, a residue is generated after the brazing material is melted. Impairs wet spread.
More preferably, the lower limit is 1000 and the upper limit is 10,000.
<Organic resin content>
Organic resin interposed amount is not particularly restricted but the present invention, the range of 0.1g / m 2 ~5g / m 2 is desirable. If the intervening amount is 0.1 g / m 2 , it decomposes and disappears early in the brazing temperature rising process, and the oxide film growth inhibiting action is insufficient, and if it is 5 g / m 2 or more, a residue is generated after melting the brazing material. Impairs the wet spread of wax.
For the same reason, it is more desirable that the lower limit is 0.2 g / m 2 and the upper limit is 3.0 g / m 2 .

<雰囲気>
本発明は、大気中でもろう付できるが、接合状態をより安定させるには減圧をともなわない不活性ガス、或いは還元性ガス等の非酸化性雰囲気中でろう付けを行う方が望ましい。使用する置換ガスの種類としては、アルミニウム材の接合を得るにあたり特に限定されるものではないが、コストの観点より、不活性ガスとしては窒素、アルゴン、還元性ガスとしては水素、アンモニア、一酸化炭素を用いることが好適である。雰囲気中の酸素濃度管理範囲としては、50ppm以下が望ましい。50ppm超ではろう付対象部材の再酸化が進みやすくなる。
<Atmosphere>
Although the present invention can be brazed in the atmosphere, it is desirable to perform brazing in a non-oxidizing atmosphere such as an inert gas without reducing pressure or a reducing gas in order to further stabilize the joining state. The type of replacement gas to be used is not particularly limited in obtaining the joining of the aluminum material, but from the viewpoint of cost, the inert gas is nitrogen, argon, the reducing gas is hydrogen, ammonia, monoxide. It is preferred to use carbon. The oxygen concentration management range in the atmosphere is desirably 50 ppm or less. If it exceeds 50 ppm, the reoxidation of the brazing target member tends to proceed.

<ろう付対象部材の材質>
ろう材以外のろう付対象部材としては、一般的に用いられているアルミニウム材料であれば何れも問題なく使用可能である。
<Material of brazing target member>
As a brazing target member other than the brazing material, any commonly used aluminum material can be used without any problem.

本発明によれば、有機物樹脂が介在することで高温域まで材料表面をバリヤーして酸化皮膜の成長を抑制し、溶融ろうの流動を阻害することなく良好なろう付性が得られる効果がある。   According to the present invention, the presence of an organic resin barriers the material surface to a high temperature range, suppresses the growth of the oxide film, and has an effect of obtaining good brazing properties without inhibiting the flow of the molten solder. .

本発明の一実施形態におけるろう付前の状態を示す概略図である。It is the schematic which shows the state before brazing in one Embodiment of this invention. 本発明の実施例におけるろう付評価モデルを示す図であるIt is a figure which shows the brazing evaluation model in the Example of this invention.

以下に、本発明の一実施形態を説明する。
ろう材用アルミニウム合金として、質量%で、Mg:0.2〜3.0%、Si:3〜12%を含有し、所望により、Bi:0.02〜0.3%を含有し、残部がAlおよび不可避不純物からなる組成に調製する。また、芯材用アルミニウム合金として、例えば、質量%で、Mn:0.2〜2.5%、Cu:0.05〜1.0%、Si:0.1〜1.2%の内1種または2種以上を含有し、残部がAlと不可避不純物からなる組成に調製する。
Hereinafter, an embodiment of the present invention will be described.
As an aluminum alloy for brazing filler metal, it contains Mg: 0.2 to 3.0%, Si: 3 to 12% by mass, and optionally contains Bi: 0.02 to 0.3%, and the balance. Is prepared to a composition comprising Al and inevitable impurities. Moreover, as an aluminum alloy for core materials, it is 1 in mass%, Mn: 0.2-2.5%, Cu: 0.05-1.0%, Si: 0.1-1.2%, for example It contains seeds or two or more species, and the balance is prepared to be composed of Al and inevitable impurities.

熱間圧延、冷間圧延を行って芯材の一方または両方の面にろう材が重ね合わされて接合されたクラッド材を得る。
上記工程を経ることにより、アルミニウム合金芯材2の一方の面にアルミニウム合金ろう材3がクラッドされた熱交換器用のアルミニウム合金ブレージングシート1が得られる。
アルミニウム合金ブレージングシート1は、熱交換器のチューブ、ヘッダ、タンクなどとして用いることができる。
Hot rolling and cold rolling are performed to obtain a clad material in which a brazing material is superposed on one or both surfaces of the core material and joined.
By passing through the said process, the aluminum alloy brazing sheet 1 for heat exchangers in which the aluminum alloy brazing material 3 was clad on one surface of the aluminum alloy core material 2 is obtained.
The aluminum alloy brazing sheet 1 can be used as a heat exchanger tube, header, tank, or the like.

一方、ろう付け対象部材4として、例えば、質量%で、Mg:0.1〜0.8%、Si:0.1〜1.2%を含有し、残部がAlと不可避不純物からなるアルミニウム合金を調製し、適宜形状に加工される。   On the other hand, as the brazing object member 4, for example, an aluminum alloy containing Mg: 0.1 to 0.8% and Si: 0.1 to 1.2% by mass, with the balance being Al and inevitable impurities And processed into an appropriate shape.

上記アルミニウム合金ブレージングシート1は、上記アルミニウム合金ろう材3が最表面に位置しており、表面酸化皮膜の平均膜厚が15nm以下で、前記表面酸化皮膜中におけるMgO皮膜の平均膜厚が2nm以下に調整されている。
また、ろう付け対象部材5は、少なくとも接合面において表面酸化皮膜の平均膜厚が15nm以下かつ皮膜中のMgO皮膜厚さが2nm以下に調整されている。
上記表面酸化皮膜は、鋳造後の均質化、熱間圧延前の均熱、冷間圧延後の焼鈍等、各種
熱処理時の温度と時間によって調整することができる。
In the aluminum alloy brazing sheet 1, the aluminum alloy brazing material 3 is located on the outermost surface, the average film thickness of the surface oxide film is 15 nm or less, and the average film thickness of the MgO film in the surface oxide film is 2 nm or less. Has been adjusted.
Moreover, the brazing object member 5 is adjusted so that the average film thickness of the surface oxide film is 15 nm or less and the MgO film thickness in the film is 2 nm or less at least on the bonding surface.
The surface oxide film can be adjusted by temperature and time during various heat treatments such as homogenization after casting, soaking before hot rolling, and annealing after cold rolling.

上記アルミニウム合金ブレージングシート1とろう付け対象部材4とは、アルミニウム合金芯材2とろう付け対象部材4との間にアルミニウム合金ろう材3が介在するように配置し、さらに、アルミニウム合金ろう材3上に有機物樹脂による有機物樹脂層5を形成する。これらを組み付けてろう付け用アルミニウム合金組み付け体とする。これにより少なくとも接合部において有機物樹脂層5が介在している。有機物樹脂層5は、例えば塗布により形成することができる。塗布は、アルミニウム合金ろう材3表面に行ってもよく、ろう付け対象部材4表面に行ってもよく、両方に塗布を行うようにしてもよい。塗布方法としては、塗布方法は特に限定されるものではなく、スプレー法、シャワー法、フローコーター法、ロールコーター法、刷毛塗り法、浸漬法などを適宜採用することができる。   The aluminum alloy brazing sheet 1 and the brazing target member 4 are disposed such that the aluminum alloy brazing material 3 is interposed between the aluminum alloy core material 2 and the brazing target member 4. An organic resin layer 5 made of an organic resin is formed thereon. These are assembled into an aluminum alloy assembly for brazing. As a result, the organic resin layer 5 is interposed at least at the junction. The organic resin layer 5 can be formed by coating, for example. The application may be performed on the surface of the aluminum alloy brazing material 3, may be performed on the surface of the brazing target member 4, or may be performed on both. As a coating method, the coating method is not particularly limited, and a spray method, a shower method, a flow coater method, a roll coater method, a brush coating method, a dipping method, and the like can be appropriately employed.

上記組み付け体は、大気中、または、減圧を伴わない非酸化性雰囲気とされた加熱炉内に配置される。該非酸化性雰囲気は、窒素、アルゴンなどの不活性ガスまたは水素、アンモニア、一酸化炭素などの還元性ガス、あるいはこれらの混合ガスを用いて構成することができる。非酸化性雰囲気は、ろう付け加熱時には減圧を伴わず、通常は大気圧とされる。なお、非酸化性雰囲気を得る前に、置換などの目的で減圧工程を含むものであってもよい。加熱炉は密閉した空間を有することを必要とせず、ろう付け材の搬入口、搬出口を有するものであってもよい。このような加熱炉でも、不活性ガスを炉内に吹き出し続けることで非酸化性が維持される。該非酸化性雰囲気としては、酸素濃度として体積比で50ppm以下が望ましい。   The assembly is disposed in the heating furnace in the atmosphere or in a non-oxidizing atmosphere without decompression. The non-oxidizing atmosphere can be configured using an inert gas such as nitrogen or argon, or a reducing gas such as hydrogen, ammonia or carbon monoxide, or a mixed gas thereof. The non-oxidizing atmosphere is not at reduced pressure during brazing heating and is usually at atmospheric pressure. In addition, before obtaining a non-oxidizing atmosphere, you may include a pressure reduction process for the purpose of substitution. The heating furnace does not need to have a sealed space, and may have a brazing material carry-in port and a carry-out port. Even in such a heating furnace, the non-oxidizing property is maintained by continuously blowing the inert gas into the furnace. The non-oxidizing atmosphere preferably has an oxygen concentration of 50 ppm or less by volume.

上記雰囲気下で、例えば、昇温速度10〜200℃/minで加熱して、560〜620℃で加熱をしてろう付けを行う。
ろう付条件において、有機物塗膜の熱分解完了温度が400℃〜560℃となるため、高温域まで材料表面をバリヤーして酸化皮膜の成長を抑制するが、Al−Si−Mgろう材が溶融する時点では殆ど炭化物残渣が存在しないため、溶融ろうの流動を阻害することなく良好なろう付を行うことができる。
なお、上記実施形態では、アルミニウム合金芯材とアルミニウム合金ろう材とをクラッ
ドしてろう付け対象部材と接合するものとして説明したが、ろう付け対象部材間にアルミニウム合金ろう材を配置してろう付け接合することも可能である。
Under the above atmosphere, for example, heating is performed at a heating rate of 10 to 200 ° C./min, and heating is performed at 560 to 620 ° C. to perform brazing.
Under the brazing conditions, the thermal decomposition completion temperature of the organic coating becomes 400 ° C to 560 ° C, so that the material surface is barriered to a high temperature range to suppress the growth of the oxide film, but the Al-Si-Mg brazing material is melted. At this time, since there is almost no carbide residue, good brazing can be performed without hindering the flow of the molten solder.
In the above embodiment, the aluminum alloy core material and the aluminum alloy brazing material are clad and joined to the brazing target member. However, the brazing is performed by placing the aluminum alloy brazing material between the brazing target members. It is also possible to join.

以下に、本発明の実施例を説明する。
表1、2に示す組成(残部はAlと不可避不純物)のAl−Si−Mg系ろう材と、JIS A3003アルミニウム合金とをクラッドしたアルミニウム材を用意した。
アルミニウムクラッド材は、各種組成ろう材をクラッド率10%とし、H14相当調質の0.25mmに仕上げた。また、ろう付け対象部材としてJIS A 3005合金、H14のアルミニウムベア材(0.1mm厚)のフィン材を用意した。
前記アルミニウムクラッド材を用いて幅20mmのチューブ12を製作し、該チューブと前記コルゲートフィン11とを組み合わせ、ろう付評価モデルとして図2に示すようなチューブ15段、長さ300mmのコア10とした。その際、少なくともチューブ12とフィン11との接合部に、表2に示す組成物を表3に示す塗布量で塗布した。組成物を塗布した前記コアを、窒素雰囲気中(酸素含有量50ppm)のろう付炉にて、560〜600℃にまで加熱し、そのろう付状態を評価した。
Examples of the present invention will be described below.
The aluminum material which clad the Al-Si-Mg type | system | group brazing material of the composition shown in Table 1 and 2 (the remainder is Al and an unavoidable impurity) and the JIS A3003 aluminum alloy was prepared.
As the aluminum clad material, various composition brazing materials were made to have a clad rate of 10% and finished to a 0.25 mm tempered equivalent to H14. Further, a JIS A 3005 alloy, H14 aluminum bare material (0.1 mm thick) fin material was prepared as a brazing target member.
A tube 12 having a width of 20 mm is manufactured using the aluminum clad material, and the tube and the corrugated fin 11 are combined to form a core 10 having 15 stages of tubes and a length of 300 mm as shown in FIG. 2 as a brazing evaluation model. . At that time, the composition shown in Table 2 was applied at the application amount shown in Table 3 to at least the joint portion between the tube 12 and the fin 11. The said core which apply | coated the composition was heated to 560-600 degreeC in the brazing furnace in nitrogen atmosphere (oxygen content 50ppm), and the brazing state was evaluated.

○ろう付性
・ 接合率
以下式にて接合率を求め、各試料間の優劣を評価した。
フィン接合率=(フィンとチューブの総ろう付け長さ/フィンとチューブの総接触長さ)×100(%)
判定は以下の基準によって行い、その結果を表3に示した。
ろう付け後のフィン接合率 ◎:95%以上、○:90%以上、△:80%以上、×:80%未満
○ Brazing property / joining rate The joining rate was calculated by the following formula, and the superiority or inferiority of each sample was evaluated.
Fin joint ratio = (total brazing length of fin and tube / total contact length of fin and tube) x 100 (%)
The determination was made according to the following criteria, and the results are shown in Table 3.
Fin joint ratio after brazing ◎: 95% or more, ○: 90% or more, Δ: 80% or more, ×: less than 80%

・ろう付後の残渣
ろう付後の残渣を目視により以下の判断基準で評価した。
○:残渣がみられなかったもの
△:機微な残渣がみられたもの(数か所に点在)
×:明瞭に残渣が認められたもの(塗布部のほぼ全面に存在)
実施例の何れも良好なろう付性を示したのに対し、比較例では十分な接合が得られなかった。
-Residue after brazing The residue after brazing was visually evaluated according to the following criteria.
○: No residue was found △: Sensitive residue was found (dotted in several places)
X: The residue was clearly recognized (present on almost the entire coated area)
While all of the examples showed good brazing properties, the comparative example did not provide sufficient bonding.

Figure 2016179494
Figure 2016179494

Figure 2016179494
Figure 2016179494

Figure 2016179494
Figure 2016179494

1 アルミニウムクラッド材
2 芯材
3 Al−Mg−Si系ろう材
4 ろう付対象部材
5 有機樹脂層
10 コア
11 コルゲートフィン
12 チューブ
DESCRIPTION OF SYMBOLS 1 Aluminum clad material 2 Core material 3 Al-Mg-Si type brazing material 4 Brazing object member 5 Organic resin layer 10 Core 11 Corrugated fin 12 Tube

Claims (5)

質量%でMgを0.2〜3.0%、Siを3〜12%含有するAl−Si−Mg系ろう材をアルミニウム合金芯材に貼り合せたクラッド材を用いてアルミニウム材同士をろう付する方法であって、
少なくとも、前記Al−Si−Mg系ろう材とアルミニウム被接合部材との接合部において、ろう付前にC、H、Oのみからなる有機物樹脂を介在させ、ろう付加熱時に前記有機物樹脂により得られる炭化物膜で接合部表面を雰囲気からバリヤーし、酸化物を除去するためのフラックスを用いないことを特徴とするアルミニウム材のろう付方法。
Aluminum materials are brazed to each other using a clad material in which an Al-Si-Mg brazing material containing 0.2 to 3.0% Mg and 3 to 12% Si is bonded to an aluminum alloy core material. A way to
At least at the joint between the Al—Si—Mg-based brazing material and the aluminum member to be joined, an organic resin consisting only of C, H, O is interposed before brazing, and is obtained by the organic resin at the time of brazing addition heat. A method for brazing an aluminum material, characterized in that a carbide film is used to barrier the surface of the joint from the atmosphere and no flux is used to remove oxides.
前記有機物樹脂を数平均分子量300〜60000として、0.1〜5g/mの量で前記接合部に介在させることを特徴とする請求項1記載のアルミニウム材のろう付方法。 Wherein the organic resin as the number average molecular weight from 300 to 60,000, brazing method of the aluminum material according to claim 1, wherein the interposing said joint in an amount of 0.1-5 g / m 2. 前記炭化物膜は、ろう付昇温過程でろう材融点に到達するまでに蒸散することを特徴とする請求項1または2に記載のアルミニウム材のろう付方法。   3. The aluminum material brazing method according to claim 1, wherein the carbide film evaporates before reaching a melting point of the brazing material in a brazing temperature rising process. 前記有機物樹脂が、エポキシ樹脂、または、エポキシ樹脂と他の樹脂の混合物、または、エポキシ基またはエポキシ環が重合された樹脂であることを特徴とする請求項1〜3のいずれか1項に記載のアルミニウム材のろう付方法。   The organic resin is an epoxy resin, a mixture of an epoxy resin and another resin, or a resin in which an epoxy group or an epoxy ring is polymerized. Method of brazing aluminum material. 前記Al−Si−Mg系ろう材に、質量%で0.02〜0.3%のBiを含有することを特徴とする請求項1〜4のいずれか1項に記載のアルミニウム材のろう付方法。   The brazing of an aluminum material according to any one of claims 1 to 4, wherein the Al-Si-Mg-based brazing material contains 0.02 to 0.3% Bi by mass%. Method.
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Publication number Priority date Publication date Assignee Title
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JPH01240689A (en) * 1988-03-18 1989-09-26 Kobe Steel Ltd Surface treated aluminum fin material for heat exchanger and its manufacture
JP2000225461A (en) * 1999-02-04 2000-08-15 Sky Alum Co Ltd Drawn cup laminated type heat exchanger and brazing method
JP2010247209A (en) * 2009-04-17 2010-11-04 Mitsubishi Alum Co Ltd Fluxless brazing method for aluminum material and aluminum cladding material for fluxless brazing
JP2013204076A (en) * 2012-03-28 2013-10-07 Mitsubishi Alum Co Ltd Fin material for air-conditioning heat exchanger and air-conditioning heat exchanger
JP2014136235A (en) * 2013-01-16 2014-07-28 Mitsubishi Alum Co Ltd Brazing method of aluminum material, and aluminum material
US20140246483A1 (en) * 2011-11-11 2014-09-04 Aleris Rolled Products Germany Gmbh Aluminium alloy sheet product or extruded product for fluxless brazing

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* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS50126552A (en) * 1974-03-12 1975-10-04
JPH01240689A (en) * 1988-03-18 1989-09-26 Kobe Steel Ltd Surface treated aluminum fin material for heat exchanger and its manufacture
JP2000225461A (en) * 1999-02-04 2000-08-15 Sky Alum Co Ltd Drawn cup laminated type heat exchanger and brazing method
JP2010247209A (en) * 2009-04-17 2010-11-04 Mitsubishi Alum Co Ltd Fluxless brazing method for aluminum material and aluminum cladding material for fluxless brazing
US20140246483A1 (en) * 2011-11-11 2014-09-04 Aleris Rolled Products Germany Gmbh Aluminium alloy sheet product or extruded product for fluxless brazing
JP2013204076A (en) * 2012-03-28 2013-10-07 Mitsubishi Alum Co Ltd Fin material for air-conditioning heat exchanger and air-conditioning heat exchanger
JP2014136235A (en) * 2013-01-16 2014-07-28 Mitsubishi Alum Co Ltd Brazing method of aluminum material, and aluminum material

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