JP5210001B2 - Non-flux brazing base material, brazing method and brazed product - Google Patents

Description

  The present invention is a technique for producing a high-strength brazed product by brazing a non-flux brazing sheet with an aluminum alloy brazing sheet in an inert gas atmosphere using a base material made of a high-strength aluminum alloy containing Mg. It is about.

  In recent years, mainly from the viewpoint of weight reduction of automobiles and global environmental problems, there has been a strong demand for thinner and higher strength materials for heat exchangers of automobiles.

As this type of heat exchanger material, aluminum alloys are generally used. However, as an aluminum alloy for heat exchangers, the most simple and effective method for reducing the thickness and increasing the strength is as a solid solution. A method of adding Mg as a strengthening element is known. On the other hand, when assembling a heat exchanger, it is necessary to braze, but a dense and stable oxide film is usually formed on the surface of the aluminum alloy. It is known that the brazing property is remarkably inhibited even though the thickness is as thin as about 100 mm. Therefore, when brazing an aluminum alloy, it is necessary to destroy the oxide film on the surface, but as a method for brazing by destroying the oxide film,
A: A flux-free method in vacuum in which Mg is added to the brazing material and the coating is destroyed.
B: Non-corrosive flux method in an inert gas atmosphere,
C: Corrosive flux method in the atmosphere
The above three brazing methods are mainly used.

  Among these methods A to C, in the brazing of flux in an inert gas atmosphere of B, the brazing property is lowered due to the reaction between the flux and Mg, so that the strength of the base material (base plate) is improved. Mg, which is a solid solution strengthening element that contributes, can hardly be added, and this is a drawback in brazing in an inert gas atmosphere.

  For such a problem, for example, as shown in Non-Patent Document 1, a method of performing flux-free brazing in a nitrogen gas atmosphere using a brazing sheet of an Al—Si—Mg—Bi brazing material is proposed. Has been. However, this method has problems such as the need to control the oxide film of the base material thinly, and the need to increase the nitrogen gas flow rate during brazing to prevent oxidation.

  On the other hand, Patent Document 1 proposes a brazing sheet that improves these points and is suitable for brazing without flux in a non-oxidizing atmosphere. This proposed brazing sheet has a structure in which an aluminum thin skin material having a melting point higher than that of the brazing material is provided on the surface, and an Al-Si-Mg-Bi brazing material is sandwiched between the thin skin material and the core material. Thus, the surface thin skin material suppresses the oxidation of the surface until the time of melting the brazing, and when the brazing starts to melt, brazing is possible by leaching the liquid phase to the surface. Here, Mg in the brazing material is considered to play a role of effectively modifying the surface of the counterpart material, and a region where the Mg vapor is concentrated locally in the vicinity of the surface of the member to oxidize the brazing liquid. It is understood that it prevents the wax and ensures the spreading of the wax. In the case of this proposed technique, brazing using an Mg additive is possible, which is advantageous for improving the strength of the product.

  However, according to experiments by the present inventors, it was confirmed that even when the above-mentioned proposed brazing sheet was used, when the mating material (base material) was an alloy containing a large amount of Mg, the joint was unhealthy. Has been. This is considered to be because Mg oxide is formed in a large amount on the surface of the base material during the manufacturing of the base material or in the brazing heating process, and the wetting and spreading of the Al—Si brazing material is hindered. .

  Patent Document 2 discloses a technique that can be brazed without flux. In the proposed technique, an oxide film or a hydroxide film (specifically, more than 25 nm and less than 1000 nm) thicker than the natural oxide film is formed on the surface of the aluminum alloy. By controlling the thickness of such a film, its flexibility is reduced, and it is easily broken by thermal stress, resulting in cracks. Removal of the film occurs. In this proposal, boehmite treatment is shown as a specific film forming method, and an anodic oxidation method is also possible. However, in the case of this proposal, it is described that a lubricant containing halogen is applied to the surface while not using a flux, which may substantially play a role of flux. Here, the above proposal is difficult to reproduce because there is no specific description of the technology, but it is necessary to form a relatively thick film as described above on the brazing material. A relatively thick oxide film is also present on the surface, and the film remains after brazing, which is considered to cause a problem in bonding strength.

  Further, Patent Document 3 discloses a technique capable of brazing without flux. In the proposed technique, Mg and Bi are added to an Al—Si brazing material, and the thickness of the surface oxide film of the aluminum alloy is treated with an aqueous solution of an inorganic acid to reduce the Mg concentration near the surface. At the same time, the oxide film thickness is extremely reduced to 20 mm or less while the normal oxide film thickness is 100 to 200 mm. And by doing this, the Mg evaporation distance from the brazing material is shortened, and the getter action of Mg works more effectively, thereby making it possible to reduce the oxygen concentration in the furnace and enable flux-free brazing Yes. Further, in the proposed technique, volatile molding oil mainly composed of mineral oil is applied for the purpose of preventing the growth of the oxide film after the film is removed. In this case, the molding oil can be easily removed by heat treatment before brazing heating by thinning the oxide film, and therefore it is not necessary to perform degreasing or the like.

However, in the technique proposed in Patent Document 3, as described above, it is necessary to perform various treatments before brazing and heating after manufacturing the material, which greatly increases the manufacturing cost and is difficult to put into practical use. Seem. In addition, since the material is manufactured by hot rolling or tempering, the thickness of the oxide film may be unevenly formed. Therefore, the thickness of the oxide film is uniformly controlled during the treatment with an inorganic acid. This is not always easy.
Welding Journal, October 1983, P31-38 Japanese Patent Laid-Open No. 2001-300762 JP-T-2007-504954 Japanese Patent Laid-Open No. 10-180489

The present invention has been made against the background described above, and is based on the premise of using a brazing base material made of an aluminum alloy to which Mg is added for high strength. Provides a brazing base material that can be brazed to an aluminum alloy brazing sheet with excellent brazing properties in a non-flux, inert gas atmosphere, in a simpler, easier and less expensive manner. brazing method using the brazing sheet suitable therefor Te, it is an object of the present invention to provide a brazing product.

  In order to find a means for solving the above-mentioned problems, the present inventors have conducted various experiments and studies, and as a result, appropriately controlled the surface state of the brazing base material, particularly the state of the oxide film. The present inventors have found that the above-described problems can be solved, and have made the present invention.

  Specifically, the flux-free brazing base material of the invention of claim 1 contains Mg 0.1 to 3.0%, and the balance is made of an aluminum alloy consisting of Al and inevitable impurities. Among the surfaces, at least the surface following the surface to be brazed and joined is covered with an anodized film having a thickness of 1 to 5 μm, except for the surface to be brazed and brazed. The surface to be bonded is covered with a natural oxide film.

  The base material for flux-free brazing according to the invention of claim 2 is made of an aluminum alloy containing 0.1 to 3.0% Mg and 0.5 to 1.5% Mn, with the balance being Al and inevitable impurities. It is a base material for brazing, and at least the surface of the surface excluding the surface to be brazed and joined to the surface to be brazed is covered with an anodized film having a thickness of 1 to 5 μm. And the surface to be brazed is covered with a natural oxide film.

Further claims 3, of the invention of claim 4, Ru der those defined for brazing method for brazing the brazing preform as described above.
Brazing method of the invention of claim 3 of its, relative to the brazing preform according to claim 1 or claim 2, the surface of the core made of an aluminum alloy, Si5.0～15.0% A brazing sheet containing Mg, 0.05 to 2.0%, Bi 0.02 to 0.2%, the balance being Al and unavoidable impurities is clad, and an inert gas atmosphere without flux der those characterized by brazing at medium Ru.
Brazing method of the invention or the fourth aspect, with respect to the brazing preform according to claim 1 or claim 2, the surface of the core material made of an aluminum alloy, Si5.0～15.0% , Mg 0.05 to 2.0%, Bi 0.02 to 0.2%, with the balance being clad with a brazing material consisting of Al and inevitable impurities, and the brazing material surface has a melting point higher than that of the brazing material A brazing sheet having a coating layer made of an aluminum alloy having a high thickness and containing substantially no Mg is formed with a thickness of 0.05 to 10 μm, and is brazed in an inert gas atmosphere without flux. To do.

Furthermore the invention of claim 5, which has defined for filtration cormorants with product, brazed products in this fifth aspect, a feature that it has been obtained by the brazing method according to claim 3 or claim 4 To do.

According to the brazing base material of the present invention, the flux-free brazing in an inert gas atmosphere is applied as a high-strength brazing base material to which Mg is added. Brazing can be performed with good brazing and high bonding strength without causing problems such as instability and unstable operation. Also according to the brazing method of the octopus invention can be implemented with a really industrial stability brazing as described above. Moreover, the brazed product of the present invention can exhibit sufficient bonding strength and durability as a heat exchanger or the like.

  The brazing base material of the present invention is for brazing using a brazing sheet without flux in an inert gas atmosphere, and its basic alloy component composition is Mg to increase strength. In particular, Mg may be contained within a range of 0.1 to 3.0%, and the balance may be Al and inevitable impurities. In some cases, in addition to Mg as described later, What added Mn in 0.5 to 1.5% of range may be used.

  Furthermore, an important point in the base material for brazing of the present invention is that the state of the oxide film on the surface is divided into the surface to be brazed and the other surface (surface not to be brazed), It was decided to control appropriately. That is, as schematically shown in FIG. 1, among the surfaces of the base material 1, the surface to be brazed to the brazing sheet 2 (the lower surface of the base material 1 in FIG. 1) is forced to be anodized. The surface is not covered with an oxide film by an artificial oxidation treatment, that is, the surface is covered only with the natural oxide film 1A, and follows the other surface of the base material, particularly at least the surface to be brazed. The surface of the portion (the portion adjacent to the surface to be brazed) is covered with an anodized film 1B having a thickness of 1 to 5 μm. In FIG. 1, a brazing sheet 2 includes a brazing material 2B, 2B clad on the surface of a core material 2A made of an aluminum alloy, and a coating layer made of an aluminum alloy having a melting point higher than that of the brazing material, as will be described later. 2C and 2C are shown as being clad, but the covering layers 2C and 2C may be omitted depending on circumstances.

  By setting the coating state as described above on the outer surface of the base material, even a high strength base material containing a large amount of Mg can form a sufficient fillet and achieve a sound joint.

  That is, as shown in an enlarged view in FIG. 2, with the temperature increase in the brazing state, a very slight gap is generated in the portion following the joint surface due to the difference in thermal expansion between the anodized film and the base material. Then, the molten brazing due to the melting of the brazing material 2B of the brazing sheet 2 enters along the gap, and as a result, while the anodized film is pushed up, its deformation and destruction progress, and a sufficiently large fillet 5 is formed.

  Here, if Mg in the base material is exposed on the surface, even if brazing in an inert gas atmosphere, a large amount of Mg oxide is formed on the surface before the start of brazing, Therefore, even if the brazing material is melted, the wetting and spreading of the molten brazing is significantly hindered by the Mg oxide, but in the case of the brazing base material of the present invention, the portion of the base material following the brazing joint surface Since there is an anodized film on the surface, the formation of Mg oxide is prevented at that part, and the molten wax penetrates into the interface between the anodized film and the base material. The problem can be avoided.

  Furthermore, a natural oxide film (usually 100 to 200 angstroms thick) is formed on the brazing joint surface of the base material, and this surface is brazed and heated in a state of surface contact with the brazing sheet. Even during heating and heating, excessive surface oxidation does not occur, and the problem of impeding the spread of the molten wax does not occur. On the other hand, Mg evaporated from the base material containing Mg modifies the oxide film of the brazing material of the brazing sheet, so that the natural oxide film on the surface of the base material is quickly damaged at this part when the solder is melted. Will spread out. Therefore, there is no need to make the oxide film extremely thin as shown in Patent Document 3 described above. That is, in the case of the present invention, brazing is performed in an inert gas atmosphere, but there is usually a small amount of oxygen in the atmosphere, and in that case, a base material containing a large amount of Mg. When Mg evaporated from the inside is combined with oxygen in the atmosphere, it acts to lower the oxygen concentration in the nearby atmosphere (getter action), so that an extremely low oxygen state is maintained near the joint surface, and a healthy brazing flow This is one of the factors that can ensure bonding.

  As described above, by using a base material containing high Mg, by appropriately controlling the state of the oxide film on the brazed joint surface and other surfaces (particularly at least the surface of the portion following the brazed joint surface), It is possible to form a large fillet to obtain a sound joint and thereby to obtain a sufficient joint strength without incurring an inhibiting factor of the brazing joint such as the inhibition of the spreading of the brazing material.

  Further, the constituent requirements of the brazing base material of the present invention will be described in detail.

  As described above, the base metal alloy basically contains 0.1 to 3.0% of Mg, and the balance is made of Al and inevitable impurities.

  Here, if the Mg content is less than 0.1%, the high strengthening of the base material is insufficient, and the getter effect due to Mg cannot be obtained sufficiently, while if the Mg content exceeds 3.0%, Since the Mg vapor in the atmosphere during brazing heating becomes an excessive amount, adhesion of Mg oxide to the surface of the brazing sheet may occur, and brazing property may be lowered. It was made into the range of -3.0%. The Mg content of the base material is more preferably within the range of 0.3 to 0.8%.

  Furthermore, as a base material alloy, Mn may be contained in the range of 0.5 to 1.5% in addition to Mg.

  Mn is an element effective for improving the strength. However, if Mn is less than 0.5%, the effect cannot be sufficiently obtained. On the other hand, if the amount of Mn exceeds 1.5%, a giant intermetallic compound is crystallized, Since there is a possibility of inhibiting the manufacturability and formability, the amount of Mn when adding Mn to the base metal alloy is set in the range of 0.5 to 1.5%. Of course, even when Mn is not actively added (in the case of claim 1), a case where less than 0.5% of Mn is contained as an inevitable impurity is allowed.

  In addition to Mg and Mn, the base metal alloy is 0.7% or less Cu, 0.3% or less Cr, 0.3% or less Ni, 0.3% or less Zr, 0.3% or less. It is allowed to contain one or more of V, and these elements do not adversely affect the brazeability within the above range. Here, Cu contributes to strength improvement, and Cr, Ni, Zr, and V also contribute to strength improvement and refinement of the crystal structure, but if Cu exceeds 0.7%, after brazing heating The heat history of the heat exchange cycle during the cooling process and use as a heat exchanger may cause Al-Cu intermetallic compounds to precipitate at the grain boundaries, which may cause intergranular corrosion, If Cr, Ni, Zr, and V each exceed 0.3%, the effects of these additions are saturated, and the economy may be impaired.

  In general aluminum alloys, a small amount of Ti is often added alone or in combination with a small amount of B for refining the structure during casting. Ti 0.15% or less and B 0.03% or less may be added.

  In addition, as an inevitable impurity of an aluminum alloy, Fe and Si are typical, but in the case of the brazing base metal alloy of the present invention, Fe as an inevitable impurity is 0.8% or less, and Si is 0.8%. The following is preferable. In addition, Zn may be added to improve corrosion resistance in an aluminum alloy, but 3.0% or less of Zn is allowed in the brazing base material of the present invention.

  The component composition of the base alloy for brazing is as described above. In practice, however, considering the product strength and corrosion resistance necessary within the range satisfying the above conditions, JIS A 1070, 1050, 1100, 1200 Standard alloys such as 3203, 3004, 5005, 5N01, 6951, 6061, 6063, and 6N01, and alloys obtained by adding some alloy elements to them may be used.

  In the brazing base material of the present invention, it is necessary that an anodic oxide film be formed on at least the surface of the surface excluding the brazed joint surface that follows the brazed joint surface. The thickness of the film needs to be in the range of 1 to 5 μm. It has been confirmed by experiments by the present inventors that it is difficult to ensure excellent brazing properties when the thickness of the anodized film is less than 1 μm and when it exceeds 5 μm. The reason is not necessarily clear, but when the thickness is less than 1 μm, a gap is formed between the anodized film and the base material at an early stage. When the thickness exceeds 5 μm, the anodized film is too thick, and it is considered that Mg to be diffused does not reach the surface. The portion where the anodized film is to be formed may be at least the surface of the portion adjacent to the brazed joint surface and continuing to the brazed joint surface, and the surface of the portion far away from the brazed joint surface. The anodized film may not be formed, but in the actual mass production process, the anodized film is often formed on the entire surface other than the brazed joint surface.

  Further, as a specific method of anodizing treatment, various methods can be applied, and it is not particularly limited. However, from the viewpoint of cost, it is preferable to apply a general sulfuric acid bath anodizing treatment. .

  On the other hand, the brazing joint surface in the base material, that is, the surface in contact with the brazing sheet is not covered with the anodized film as described above, and only a natural oxide film with a normal thickness (100 to 200 angstroms) exists. It is necessary to be in a state. Here, if the brazed joint surface is covered with the anodic oxide film, the brazed joint is hindered or the oxide remains on the joint surface and the joint strength is lowered.

  Here, the specific method for bringing only the anodized film into the brazed joint surface as described above is not particularly limited. After forming the anodic oxide film on the entire surface of the material, the typical method is to remove the anodic oxide film only on the brazed joint surface by machining or etching. A natural oxide film will be formed during this period. Alternatively, when anodizing the base material, the brazed joint surface is masked with an appropriate material, or the electrode is in contact with the base material during the anodizing process (that is, the processing liquid is By utilizing a portion that does not contact, an anodized film may be prevented from being formed on a portion (a surface that should be a brazed joint surface). In these cases, the natural oxide film existing before the anodizing treatment remains on the brazed joint surface.

  As described above, the portion where the anodic oxide film is not formed (the brazed joint surface) is covered with the natural oxide film, but this natural oxide film not only has an adverse effect on the brazing property, but rather the present invention. In the case of a high Mg base material, it is advantageous for brazing. That is, as already described, Mg added in a large amount to the base material evaporates at the time of brazing heating and brings about an oxidation suppression and reforming effect during heating, which is advantageous for improving brazing properties.

The structure of the brazing sheet used in combination with the brazing base material of the present invention is not particularly limited, but in the case of the brazing method of the invention of claim 3, it is made of an aluminum alloy. One or both sides of the core material clad with a brazing alloy containing 5-15% Si, 0.05-2.0% Mg, 0.02-0.2% Bi, the balance being Al and inevitable impurities Is used.

  Here, regarding the brazing alloy of the above brazing sheet, if the Si content is less than 5%, the braze flowability becomes poor. On the other hand, if the Si content is more than 15%, coarse Si in the industrial casting process. Particles are formed, resulting in variations in performance as a brazing material. Mg is an element that promotes the wetting and spreading property of the molten wax in an inert gas atmosphere and contributes to improving the strength. If the amount of Mg is less than 0.05%, the effect of spreading and spreading the molten solder is sufficient. In addition, there is little contribution to strength improvement. On the other hand, if Mg exceeds 2.0%, the effect of addition of Mg is saturated to impair economic efficiency, and Mg oxide increases and brazing performance is lowered. Furthermore, Bi is effective in coexisting with Mg or alone, improving the wettability and spreadability in an inert gas atmosphere, and rapidly infiltrating the molten braze into the interface between the anodized film and the base material. Become. If the amount of Bi in the brazing material is less than 0.02%, the effect cannot be sufficiently obtained. On the other hand, if the amount of Bi exceeds 0.2%, the above effect is not improved any more, and the economic efficiency is impaired. It is.

  On the other hand, the aluminum alloy as the core material of the brazing sheet is not particularly limited as long as it is applied to a general brazing sheet, and may be any aluminum alloy having a melting point higher than the brazing temperature. The most preferable core material is an AA3000 alloy, but considering the required product strength, corrosion resistance, etc., JIS A 1070, 1050, 1100, 1200, 3203, 3004, 5005, 5N01, 6951, 6061. , 6063, 6N01, etc., or alloys obtained by adding various alloy elements to these alloys can be used.

The brazing sheet used in combination with the brazing base material of the present invention is already described on the surface (one side or both sides) of the core material made of an aluminum alloy, as defined in the brazing method of claim 4. Then, a brazing material having the same composition as the above is clad, and a coating layer made of an aluminum alloy having a melting point higher than that of the brazing material and substantially not containing Mg is formed on the brazing material surface with a thickness of 0.05 to 10 μm. Those made are also suitable.

  As described above, since the coating layer having a melting point higher than that of the brazing material and substantially not containing Mg exists on the surface of the brazing material, a brazing material containing Mg as described above may be used. Further, it is possible to suppress the generation of Mg oxide on the surface of the brazing material during the brazing heating, and it is possible to secure even better brazing properties.

  Here, the specific component composition of the aluminum alloy of the coating layer is not particularly limited, and the point is that the melting point is higher than that of the brazing material and substantially does not contain Mg (specifically, ordinary aluminum The amount of Mg in the alloy may be less than the amount of Mg, that is, the amount of Mg is about 0.01% or less. In practice, a pure aluminum alloy such as JIS A 1070, 1050, or 1100 may be used. .

  The brazing joining using the brazing base material and the brazing sheet as described above is performed by a flux-free brazing method characterized by heating in an inert gas atmosphere. As the inert gas, nitrogen is usually preferable from the viewpoint of cost, but a rare gas such as Ar may be used. The brazing furnace can be carried out in the same furnace as the industrially used Nokolok brazing furnace, and naturally the flux itself and the flux application work can be omitted. The brazing temperature is not particularly specified but is preferably 585 ° C. to 615 ° C.

  The product brazed and joined in this manner (brazed product) has at least a part of its surface having an anodic oxide film or an oxide layer crystallized by heating it. Here, a large number of cracks of about several μm are generated in the anodic oxide film on the surface of the brazing base material following the brazing joint surface during the temperature rise during brazing heating, but usually without falling off. It remains on almost the entire surface. On the other hand, the anodized film remains on the surface of the fillet portion formed by brazing heating, although it is in a state of being broken and divided. As described above, the anodic oxide film remains on the surface of the fillet portion, whereby the effect of improving the corrosion resistance and wear resistance of the portion is obtained.

  In the above, the manufacturing method of the brazing base material itself is not particularly limited, and may be manufactured according to a conventional method according to the use, shape, and required characteristics of the final brazing product.

  Moreover, the manufacturing method of the brazing sheet itself is not particularly limited, and may be manufactured in accordance with a normal brazing sheet manufacturing method or a clad material manufacturing method.

  Hereinafter, the present invention will be described in more detail based on examples. Of course, these examples do not limit the technical scope of the present invention.

  The base metal alloys (alloy codes A to O) shown in Table 1 were cast into a 40 mm-thick ingot according to a conventional method and faced, and then hot-rolled and cold-rolled, and the thickness was 0.5 mm. A plate-shaped base material was created. Regarding the tempering of the base material, annealing was performed at 400 ° C. for 2 hours to obtain a tempered O material. Although the O material is used here, the H 1n material may be used for the tempering, and it is needless to say that the material is not particularly limited.

  On the other hand, for the brazing alloy for brazing sheets shown in Table 2 (alloy codes P to W) and the coating layer alloy (alloy codes X), an ingot was produced in the same manner, and then chamfered to a thickness of 40 mm. Then, hot rolling and cold rolling were performed, and the plate thickness was adjusted so as to obtain a predetermined cladding rate. Next, the brazing material and the skin material were overlapped as shown in the section of the coating material-brazing material of the joint combination in Table 3 and the core material made of JIS 3000 series alloy separately prepared, and this was started at 480 ° C. Was rolled into a clad material having a thickness of 3 mm, cold-rolled to 0.5 mm, and then annealed at 400 ° C. for 2 hours to obtain a tempered O material brazing sheet. Although the O material is used here, it is needless to say that the tempering does not affect the brazing property even in the case of the H1n material.

In addition, the base material obtained as described above was anodized in a 15% sulfuric acid bath with a bath temperature of 18 ° C. with a current density of 1.5 A / dm ² to obtain a predetermined anodic oxide film thickness. . The base material after the anodizing treatment is cut and combined so that the cut surface where the anodized film does not exist (the surface to be the brazed joint surface) is in contact with the brazing sheet obtained as described above. A joint specimen and a cup specimen were assembled and evaluated for brazing.

  An outline of the inverted T-joint specimen is shown in FIG. 3, and an outline of the cup specimen is shown in FIG.

  In FIG. 3, an inverted T-shaped joint test piece 3 is formed by cladding brazing materials 2B and 2B on both surfaces of a core material 2A and further forming coating layers 2C and 2C on the surfaces of the brazing materials 2B and 2B as necessary. The brazing sheet 2 and the base material 1 on which the anodized film 1B is formed on the outer surface excluding the lower surface to be the brazing joint surface are arranged so that the base material 1 is located on the upper surface side. Is. Note that a natural oxide film is formed on the lower surface (the brazed joint surface) of the base material 1.

  The cup-shaped test piece 4 is formed by forming the base material 1 into a cup shape (cylindrical shape) having an outer diameter of 32 mm and anodizing it, and then trimming both ends (thus forming an anodized film on both ends). 4), a cup-shaped base material 1 is vertically arranged on the same brazing sheet 2 as shown in FIG. In both cases, the base material 1 and the brazing sheet 2 were fixed to each other with a jig (not shown).

  These test pieces were brazed and joined by heating at 600 ° C. for 3 minutes without flux in an inert gas atmosphere (nitrogen), and the formed fillet 5 was evaluated for brazeability. The oxygen concentration in the inert gas atmosphere was adjusted to be in the range of 50 to 100 ppm.

  On the other hand, as Comparative Examples (a) to (c), a combination using a base material on which no anodized film was formed on the surface, and as a Comparative Example (d), a mother having a surface anodized film as thick as 6 μm. Test pieces similar to the above were prepared by combinations using materials, and brazed without flux in an inert gas atmosphere as described above.

  Regarding the evaluation results of the brazing property, the reverse T joint test piece was evaluated by the fillet forming ability in appearance, and the cup joint test piece was similarly evaluated for the inner and outer fillets by cutting the cup. The results are shown in Table 4.

  Comparative Examples (a) to (c) were all examples in which an anodized film was not formed on the surface of the base material, but no fillet was formed in Comparative Example (a) among them. It has been confirmed that this tendency is the same even when the amount of Mg in the brazing material and the base material is increased. In Comparative Examples (b) and (c), there was no anodic oxide film, but the presence of a coating layer on the surface of the brazing material of the brazing sheet resulted in some fillets being formed, although insufficient. This is considered to be due to the antioxidant effect of the brazing material surface by the coating layer. On the other hand, Comparative Example (D) is an example in which the thickness of the anodized film on the surface of the base material is as thick as 6 μm, but no fillet was formed in this case. This is presumably because the anodized film was too thick, so that the deformation / destruction of the anodized film did not progress during brazing, and the penetration of the molten brazing did not proceed.

  On the other hand, among the examples (joints No. 1 to No. 29) in which the anodized film is formed on the base material, the brazing sheet has no coating layer and the base material and the brazing material do not contain Mg. In the comparative example 1, no fillet was formed, but the brazing sheet had no coating layer, but the base material and brazing material contained Mg. 2-No. In example 7, good fillets were formed. However, in the example (No. 7) in which the amount of the base material Mg is relatively large of 2.5% among these, the surface is slightly discolored and the fillet is slightly reduced. Further, the amount of Mg added to the base material was increased to 3.5% outside the scope of the present invention. In example 8, no fillet was formed.

  Of the examples in which the anodic oxide film is formed on the base material and the coating layer is present on the brazing sheet (joints No. 9 to No. 29), the comparative example in which the base material does not contain Mg (No. 9) In No. 13), Mg in the brazing material diffuses a little, but an extremely small fillet was formed.

  On the other hand, among the examples (No. 9 to No. 29) in which the anodic oxide film is formed on the base material and the coating layer is present on the brazing sheet, the base material component composition, the brazing sheet coating material, and the brazing material component composition In the case of any of the present invention examples (No. 10 to No. 12, No. 14 to No. 21, No. 24, No. 25, No. 27, No. 28) within the range defined by the present invention. In any case, a good fillet was formed.

  On the other hand, No. in which the amount of Mg added to the base material is excessive. In Comparative Example 22, no fillet was formed, and the surface discoloration was large.

  In addition, the Mn content in the base material is excessive. In Comparative Example 23, although a small fillet was formed, it was confirmed that the ear height and the like became unstable during cup molding. Accordingly, it is necessary to select the amount of Mn added from the viewpoint of moldability and the like.

  Furthermore, although the component composition of the base material is within the range specified in the present invention, the amount of Bi added to the brazing material was excessive. In the case of No. 26, discoloration of the surface considered to be segregated during annealing was observed.

  No. 18-No. From 20 examples, it has been confirmed that the addition of a small amount of Zn, Cr, Ti to the base material does not adversely affect the brazeability.

  Furthermore, brazing joint strength was evaluated as follows.

That is, as a base material, a plate material having a thickness of 0.5 mm with an alloy code C shown in Table 1 is formed into a strip shape having a width of 20 mm and a length of 110 mm, masking from one end to 10 mm, and then using a 15% sulfuric acid bath. The anodic oxidation treatment was carried out so that the portions other than the masking portion were covered with an anodic oxide film having a thickness of 2 μm or 4 μm. At this time, the bath temperature was 18 ° C. and the current density was 1.5 A / dm ² . On the other hand, a three-layer brazing sheet made of a core material made of 3003 alloy and a brazing material of alloy code R shown in Table 2 (both sides; each clad rate of 15%) was prepared by a conventional method. A strip shape having a length of 110 mm was used. Combining these base materials and brazing sheets, the base materials are fixed so that they both wrap at a portion where no anodized film exists, and brazing heat is applied at 600 ° C. for 3 minutes in a nitrogen atmosphere. No. 5 30, no. The joint shown in 31 was created.

  Further, as a comparative example, the above-mentioned strip made of the base material was anodized without masking, combined with the same brazing sheet as a wrap length of 10 mm, brazed and joined in the same manner as described above. 32, no. The joint shown in 33 was created.

  About these, while observing the state after joining, the tensile test was done in the longitudinal direction and the strength of joining was evaluated.

  FIG. 5 schematically shows the shape of the tensile test piece 6 and Table 5 shows the results of observation of the joining state and the tensile test results.

As is apparent from Table 5, it was confirmed that a sound fillet was formed at the joint in the present invention example. In addition, even when this was subjected to a tensile test, it was confirmed that the material was broken at the base material side, that is, the strength of the joint was high. In addition, by using an alloy containing Mg as a base material in this way, it was confirmed that the strength of the base material after joining was also improved by 60 to 70 N / mm ² from the normal 3003 alloy.

  On the other hand, in the case of the comparative example in which the anodized film on the brazed joint surface was not removed, the joining was poor. Among them, when the thickness of the anodic oxide film was 2 μm, some fillets were formed. However, when the tensile test was performed, it was broken from the joint portion, and the breaking load was varied and extremely low. This is presumably because the bonding strength was lowered due to the anodic oxide film remaining on the bonding surface.

2 is a longitudinal cross-sectional view schematically showing a part of a brazing base material of the present invention together with a brazing sheet. It is a longitudinal cross-sectional view which expands and shows typically the state after brazing joining of the base material for brazing shown in FIG. It is a schematic diagram which shows the outline | summary of the inverted T-shaped specimen for the brazing bondability test in the Example of this invention. It is a schematic diagram which shows the cup test piece for the brazing bondability test in the Example of this invention. It is a schematic diagram which shows the tensile test piece for the joint strength test in the Example of this invention.

Explanation of symbols

DESCRIPTION OF SYMBOLS 1 Base material 1A Natural oxide film 1B Anodized film 2 Brazing sheet 2A Core material 2B Brazing material 2C Coating layer 5 Fillet

Claims (5)

It is a base material for brazing made of an aluminum alloy containing Mg 0.1 to 3.0% (mass%, hereinafter the same), the balance being Al and inevitable impurities,
Of the surfaces except for the surface to be brazed, at least the surface following the surface to be brazed is covered with an anodized film having a thickness of 1 to 5 μm and brazed. A base material for flux-free brazing characterized in that the power surface is covered with a natural oxide film. It is a base material for brazing made of an aluminum alloy containing Mg 0.1 to 3.0%, Mn 0.5 to 1.5%, the balance being Al and inevitable impurities,
Of the surfaces except for the surface to be brazed, at least the surface following the surface to be brazed is covered with an anodized film having a thickness of 1 to 5 μm and brazed. A base material for flux-free brazing characterized in that the power surface is covered with a natural oxide film. For the brazing base material according to claim 1 or claim 2 ,
A brazing material containing Si 5.0 to 15.0%, Mg 0.05 to 2.0%, Bi 0.02 to 0.2% on the surface of the core material made of an aluminum alloy, the balance being Al and inevitable impurities A brazing method comprising brazing a brazing sheet clad with a no-flux in an inert gas atmosphere. For the brazing base material according to claim 1 or claim 2 ,
The surface of the core material made of an aluminum alloy contains Si 5.0 to 15.0%, Mg 0.05 to 2.0%, Bi 0.02 to 0.2%, and the balance will be made of Al and inevitable impurities. A brazing sheet in which a coating layer made of an aluminum alloy having a melting point higher than that of a brazing material and containing substantially no Mg is formed on the surface of the brazing material with a thickness of 0.05 to 10 μm. A brazing method characterized by brazing in an inert gas atmosphere without flux. A brazed product obtained by the brazing method according to claim 3 or 4.

Images