JP5832348B2 - Aluminum alloy coated plate - Google Patents

Description

  The present invention relates to an aluminum alloy coated plate used in contact with a galvanized steel plate or a zinc-aluminum plated steel plate.

Members that combine steel and aluminum (alloy) materials are lightweight, high-strength, and also have resistance to collisions. In recent years, their needs have increased mainly in the field of transportation equipment such as automobiles and railway vehicles. Yes.
Usually, when steel and aluminum are used for automobiles, the steel plate and the aluminum plate are joined by resistance welding or mechanical joining. When the steel plate and the aluminum plate are joined in a butt shape, a gap is unlikely to occur because the joined portions are in close contact. On the other hand, when the steel plate and the aluminum plate are joined by the surface, the joining surface does not completely adhere to each other, and because of distortion of the member itself or spot welding, the gap between the steel plate and the aluminum plate. , Various gaps occur. When the size of the gap (distance between the steel plate and the aluminum plate) is about 0.1 mm, in the electrodeposition coating normally used in the undercoating process at the time of automobile manufacture, the paint does not enter the gap. Unpainted parts occur on the steel and aluminum surfaces.

  When a joining member in which a steel plate and an aluminum plate are joined to each other is used as, for example, a body panel of an automobile, moisture may enter into the above-described gap during use. As a result, different metal contact corrosion (galvanic corrosion) occurs between the unpainted portion of the steel plate and the unpainted portion of the aluminum plate, and the corrosion of aluminum that is lower than steel is promoted. Dissimilar metal contact corrosion means that when different metals such as steel and aluminum are brought into contact with each other, the base metal among the different metals is the anode through the electrolyte formed by the water that has entered the gap between the contact surfaces. This is a phenomenon in which a noble metal acts as a cathode to form a battery, and corrosion of the base metal is promoted. That is, in the dissimilar metal joint structure of steel plate / aluminum plate, if the gap exists, corrosion of aluminum is promoted during use, and the corrosion rate becomes much higher than that of aluminum alone, and damage such as perforation occurs early. Is caused. Therefore, it is necessary to prevent such different metal contact corrosion in members / parts formed by surface bonding of different metals.

Conventionally, the following methods have been proposed as a method for preventing contact corrosion of different metals.
For example, a technique for electrically insulating different kinds of metals via an insulator has been proposed (see Patent Document 1). In addition, a technique has been proposed in which a pre-coated steel plate and a pre-coated aluminum plate pre-coated with an organic resin are used, and these are joined by an adhesive after forming (see Patent Document 2). Moreover, the technique which interposes a Zn-Al-Mg alloy between aluminum material and steel material is proposed (refer patent document 3). In addition, a technique for coating a contact portion of a different metal with a composition containing a nitrite inhibitor or an oxyanion inhibitor has been proposed (see Patent Document 4). Moreover, when joining a steel plate and an aluminum plate, a resin film containing at least one resin selected from polyolefin resin, polyurethane resin, and epoxy resin and silica is formed on the surface of the steel plate side. The technique to do is proposed (refer patent document 5). A technique has been proposed in which a coating film composed of a water-based urethane resin, silica, and a lubricant is formed on the surface of an aluminum material, and the coating film surface is joined to a steel material. (See Patent Document 6).

JP 2008-80394 A Japanese Patent Laid-Open No. 5-50173 JP 2001-11665 A JP-A-4-160169 JP 2011-140067 A JP 2011-156825 A

However, for example, in the technique of electrically insulating between different kinds of metals via an insulator as in Patent Document 1, there are many cases where it is difficult to actually realize because there are structural and manufacturing restrictions. Even so, there is a problem that welding superior in terms of bonding strength cannot be applied. For example, Patent Document 1 describes a method of spot welding after applying an organic resin adhesive in advance to a contact portion of a different metal. However, in this method, the construction takes time and the application state is likely to be non-uniform, which may cause corrosion from the application defect portion.
In addition, in the method of joining with an adhesive after molding processing, for example, as in Patent Document 2, contact corrosion does not occur, but since an adhesive is used for joining, work is troublesome and the joining strength is increased. There is a problem in application to a structural member such as a body panel of an automobile, which is not reliable.

Further, as disclosed in Patent Document 3, in a method in which a Zn—Al—Mg alloy is interposed, a Zn—Al—Mg alloy layer must be formed by means such as plating, which makes the process complicated.
Further, as disclosed in Patent Document 4, the method of coating with a composition containing an inhibitor is effective for suppressing contact corrosion between stainless steel or titanium having a higher potential than steel materials and general steel materials. However, it cannot be applied to suppression of contact corrosion with a metal having a low potential (for example, aluminum).
Further, as in Patent Documents 5 and 6, the method of adding silica to the single layer film has a problem that the continuity of the anticorrosion effect is low and it is difficult to sufficiently suppress the corrosion of aluminum.

  In a state where the steel plate and the aluminum alloy plate are in contact, when water is present in the gap, the aluminum alloy, which is a base metal rather than iron, dissolves due to electrochemical properties, and pitting corrosion occurs on the aluminum alloy plate. . In particular, in a state where a galvanized steel plate or zinc-aluminum plated steel plate generally used for automobile materials and an aluminum alloy plate are in contact with each other, zinc, which is a lower metal than an aluminum alloy, is galvanized steel plate or aluminum-zinc plated. It is easy to melt from the steel plate. When the zinc layer is consumed from the galvanized steel sheet or the zinc-aluminum plated steel sheet, the iron is exposed, the aluminum alloy is melted, and there is a risk that pitting corrosion will eventually occur on the aluminum alloy sheet. As a method for preventing corrosion of aluminum, there is a method in which a sacrificial anode layer such as zinc is clad on the surface of an aluminum material. However, since the sacrificial anode layer has low strength, in order to maintain the strength as a structural material, it is necessary to increase the thickness of the aluminum material, resulting in a problem of high cost.

  The present invention has been made in view of such a background, and is intended to provide an aluminum alloy coated plate capable of sufficiently suppressing contact corrosion on a contact surface with a galvanized steel plate or a zinc-aluminum plated steel plate. is there.

One aspect of the present invention is an aluminum alloy coated plate used in contact with a galvanized steel plate or a zinc-aluminum plated steel plate,
The aluminum alloy coated plate has a substrate made of aluminum or an aluminum alloy, and a resin coating layer A containing a resin component and metal powder formed on at least the contact surface on the steel plate side of the substrate,
The resin coating layer A is an aluminum alloy coated plate characterized by containing zinc powder and / or zinc alloy powder as the metal powder and having a surface resistance of less than 300Ω (Claim 1).

In the aluminum alloy coated plate, the resin coating layer A contains zinc powder and / or zinc alloy powder as the metal powder, and the surface resistance of the resin coating layer A is less than 300Ω. Therefore, the contact potential between the zinc layer of the galvanized steel plate or the zinc-aluminum plated steel plate and the aluminum alloy coated plate can be made closer. Therefore, even if a coating film defect occurs in the resin coating layer A, it suppresses the consumption of the zinc layer of the galvanized steel sheet or zinc-aluminum plated steel sheet when exposed to water, and the iron is exposed to aluminum. Or it can suppress that a pitting corrosion arises in the said board | substrate which consists of aluminum alloys.
Therefore, the said aluminum alloy coating plate can fully suppress the contact corrosion in a contact surface with a galvanized steel plate or a zinc-aluminum plated steel plate.

Explanatory drawing which shows the cross-section of the aluminum alloy coating board which has the resin film layer A in an Example. Explanatory drawing which shows the cross-section of the structure which made the plated steel plate and the aluminum alloy coating plate contact in an Example. Explanatory drawing which shows the cross-section of the aluminum alloy coating board which has the resin film layer A and the resin film layer B in an Example. Explanatory drawing which shows the cross-section of the aluminum alloy coating board which contains the resin bead in the resin film layer B in an Example. Explanatory drawing which shows the measuring method of the surface resistance of the resin film layer A of the aluminum alloy coating board in an Example. Explanatory drawing which shows the state which formed the crosscut part in the coating surface of the resin film layer of the aluminum alloy coating board in an Example. Explanatory drawing which shows the test piece for a corrosion test in which the coating-film surface of the resin coating layer of an aluminum alloy coating plate in an Example and a steel plate are faced, and a water retention layer is arrange | positioned among these. Explanatory drawing which shows a mode that an aluminum alloy coating board is folded and processed in an Example by a cross-sectional structure. Explanatory drawing which shows a mode that a convex part is formed in an aluminum alloy coating board by press work in an Example by sectional structure.

Next, a preferred embodiment of the aluminum alloy coated plate will be described.
The aluminum alloy coated plate is used in contact with a galvanized steel plate or a zinc-aluminum plated steel plate. For example, the said aluminum alloy coating plate is used in order to join a galvanized steel plate or a zinc-aluminum plated steel plate, and to form a joining structure. The obtained bonded structure is used as, for example, a body panel such as an automobile door. In the present specification, the galvanized steel sheet or the zinc-aluminum plated steel sheet is hereinafter simply referred to as “plated steel sheet” as appropriate. A galvanized steel plate is a steel plate plated with zinc or an alloy containing zinc as a main component, and a zinc-aluminum plated steel plate contains at least zinc and aluminum, and is plated with an alloy containing either of these as main components. Steel plate.

  The said aluminum alloy coating plate and the said plated steel plate can be joined in the state which has electrical continuity. Preferably, the aluminum alloy coated plate is used after being mechanically or chemically bonded to an unpainted steel sheet (claim 12). In this case, the weight can be significantly reduced as compared with the case where the structure is assembled with the plated steel plate alone, and higher strength can be obtained as compared with the case where the structure is assembled with the aluminum alloy plate alone. In this case, the above-described excellent contact corrosion inhibiting effect of the aluminum alloy coated plate can be remarkably exhibited. The aluminum alloy coated plate and the plated steel plate can be joined by caulking, screwing, rivets, an adhesive, or the like, for example.

Moreover, the said aluminum alloy coating plate has the board | substrate which consists of aluminum or an aluminum alloy, and the resin film layer A formed in the contact surface at least on the said steel plate side of this board | substrate.
As the substrate, for example, various aluminum alloys such as pure aluminum and 6000 series aluminum can be used.
The resin coating layer A can be formed on one side or both sides of the substrate. Moreover, it is preferable that the chemical conversion film is formed in the formation surface of the said resin film layer A in the said board | substrate. The resin coating layer A can be formed on the chemical conversion coating.
The chemical conversion film is a film that improves the adhesion between the substrate and the resin coating layer A. For example, a chemical conversion film made of phosphate chromate, zirconium phosphate, zirconium oxide, chromate chromate, or the like can be formed.

The resin coating layer A preferably contains at least one resin selected from the group consisting of epoxy-phenolic resins, epoxy-urea resins, and polyester resins as the main component of the resin component.
In this case, the acid resistance, alkali resistance, water resistance, and processability of the resin coating layer A can be improved. Epoxy-phenol resins, epoxy-urea resins (epoxy-urea resins), and polyester resins are also easily available industrially.

The epoxy-phenol resin is preferably composed of an epoxy resin having an epoxy equivalent of 145 g / eq or more and less than 450 g / eq and a resol type phenol resin.
When the epoxy equivalent is less than 145 g / eq, the resin is soft and the resin coating layer A may be easily damaged during processing. On the other hand, when the epoxy equivalent is 450 g / eq or more, the resin is hard and workability may be reduced.
Further, as the phenol resin, for example, a novolac type phenol resin can be used, but the flexibility of the resin coating layer A is lost as compared with the resol type phenol resin, and the workability may be lowered. Therefore, a resol type phenol resin is preferable.

The epoxy-urea resin is preferably composed of an epoxy resin having an epoxy equivalent of 145 g / eq or more and less than 450 g / eq and a butylated urea resin.
When the epoxy equivalent is less than 145 g / eq, the resin is soft and the resin coating layer A may be easily damaged during processing. On the other hand, when the epoxy equivalent is 450 g / eq or more, the resin is hard and workability may be reduced.

The polyester resin preferably has a number average molecular weight of 5000 to 16000, an elongation at break of 120 to 295%, and a glass transition point of 10 ° C to 60 ° C.
When the number average molecular weight of the polyester resin is less than 5000, the flexibility of the resin film is lowered, and the processability may be reduced. The number average molecular weight of the polyester resin is more preferably 10,000 or more, and further preferably 13,000 or more. On the other hand, when the number average molecular weight exceeds 16000, the resin becomes soft, and there is a possibility that tacking occurs where the coated plates stick to each other.

Moreover, when the elongation at break of the polyester resin is less than 120%, for example, the resin coating layer A cannot follow during the drawing process, and the resin coating layer A may be peeled off from the substrate. On the other hand, when the elongation at break exceeds 295%, the resin is too soft and the above-described tacking may occur. The breaking elongation of the polyester resin is more preferably 120 to 206%.
The elongation (%) of the polyester resin can be measured by a tensile test of a resin film made of the polyester resin. The ratio of the length of the resin film at the time of fracture after the tensile test to the length of the resin film before the tensile test is expressed as a percentage. The tensile test can be performed at a temperature of 25 ° C., for example.

  Moreover, when the glass transition point of the said polyester resin is less than 10 degreeC, there exists a possibility that the tacking that aluminum alloy coating plates may stick may occur easily. On the other hand, when the glass transition point exceeds 60 ° C., the flexibility of the resin coating layer is lowered, and the workability may be reduced. More preferably, the glass transition point of the polyester resin is 10 to 55 ° C.

The resin coating layer A contains zinc powder and / or zinc alloy powder as the metal powder, and has a surface resistance of less than 300Ω.
When the surface resistance of the resin coating layer A is 300Ω or more, when a coating defect occurs in the resin coating layer A, the corrosion current concentrates on the defective portion, and the zinc layer of the plated steel sheet at the counter electrode is early. There is a possibility that pitting corrosion may occur in the aluminum alloy plate due to consumption and exposure of iron. When the resin coating layer A contains at least zinc powder and / or zinc alloy powder and the surface resistance is less than 300Ω, even if a coating film defect occurs in the resin coating A, the zinc layer as a counter electrode is corroded. Current does not concentrate, and consumption of the zinc layer can be suppressed. More preferably, the resin film layer A has a surface resistance of 200Ω or less, more preferably 50Ω or less, and even more preferably 10Ω or less. A method for measuring the surface resistance of the resin coating layer A will be described later in Examples.

The resin coating layer A preferably contains 1 to 300 parts by mass of the metal powder with respect to 100 parts by mass of the resin component.
When content of the said metal powder is less than 1 mass part, there exists a possibility that the inhibitory effect of contact corrosion may become small. As for content of the said metal powder, 10 mass parts or more are more preferable, and 20 mass parts or more are further more preferable. On the other hand, when the content of the metal powder exceeds 300 parts by mass, the ratio of the resin component in the resin coating layer A decreases, and the resin coating layer A becomes brittle, for example, workability and adhesion during hem processing. May decrease. As for content of the said metal powder, 200 mass parts or less are more preferable, and 100 mass parts or less are more preferable.
The resin coating layer A contains zinc powder and / or zinc alloy powder as metal powder, but may further contain other metal powder such as aluminum powder and aluminum alloy powder. Even in this case, the total amount of these metal powders is preferably 1 to 300 parts by mass as described above.

The resin coating layer A preferably contains the zinc powder as a main component of the metal powder.
The resin coating layer A preferably contains the zinc alloy powder as a main component of the metal powder.
When the zinc powder or the zinc alloy powder is the main component of the metal powder, contact corrosion with the galvanized steel sheet or the zinc-aluminum plated steel sheet can be more sufficiently suppressed.
The zinc powder is pure Zn powder, and the zinc alloy powder is an alloy powder containing 50 mass% or more of Zn or an alloy powder containing Zn as a main component. As the zinc alloy powder, in addition to Zn, an alloy powder containing at least one metal component other than Zn, such as Al and Sn, can be used.

Examples of the zinc powder include “R powder”, “F powder” and “UF powder” manufactured by Hakusuitec Co., Ltd., “F-3000” manufactured by Honjo Chemical Co., Ltd. Zinc powder "(200 mesh pass)" or the like can be used.
As the zinc alloy powder, for example, Zn-22.3Al, Zn-2Al, Zn-50Sn, etc. manufactured by Hikari Material Industries Co., Ltd. can be used.

The resin coating layer A preferably further contains an aluminum powder and / or an aluminum alloy powder as the metal powder.
In this case, the potential of the resin coating layer A can be made more noble, and the contact potential between the zinc layer of the galvanized steel plate or the zinc-aluminum plated steel plate and the aluminum alloy coated plate can be further increased. Can be approached. Aluminum powder and aluminum alloy powder can be used as a selective component of the metal powder, and the content thereof can be 0 parts by mass. Even if it is a case where it adds, it is preferable to make the total amount (mass part) of aluminum powder and aluminum alloy powder smaller than the total amount (mass part) of zinc powder and zinc alloy powder. When the ratio of the total amount of the aluminum powder and the aluminum alloy powder increases, the chance of contact between zinc and aluminum contained in the resin coating layer A increases, zinc is consumed at an early stage due to self-corrosion, and the corrosion resistance decreases. There is a fear. More preferably, in the resin coating layer A, 0 ≦ (aluminum powder content (part by mass) + aluminum alloy powder content (part by mass)) / (zinc powder content (part by mass) + zinc alloy. It is preferable that the content (parts by mass) of the powder) ≦ 0.99.

The aluminum powder is a pure Al powder, and the aluminum alloy powder is an alloy powder containing Al as a main component.
As the aluminum powder, for example, “# 500F”, “# 600F”, “# 700F”, “# 800F”, “# 900F”, “# 1000F” manufactured by Minalco Co., Ltd. can be used.
Examples of the aluminum alloy powder include “Al-25Si-30Zn”, “Al-30Si-5Zn”, “Al-12Si-2Mg”, “Al-5Si”, “Al-10. 5Si "," Al-20Si "," Al-25Si "," Al-12Si "," Al-15Si "," Al-8Si ", and the like can be used.

The resin coating layer A is selected from the group consisting of benzoate, glutamate, anisidine, glycine, quinolinol, phthalate, adipate, and acetate with respect to 100 parts by mass of the resin component. It is preferable to contain 25 parts by mass or less of the above corrosion inhibitor (claim 6).
In this case, the corrosion resistance of the aluminum alloy coated plate can be further improved.
That is, in this case, even when the resin film is defective due to contact with or handling of a mold during bending by a press or overhang molding, for example, the corrosion inhibitor is in the resin film layer A when exposed to water. Then, the corrosion inhibitor is concentrated in the course of drying, and a hydrophobic adsorption layer can be formed on the surface of the aluminum alloy coated plate. This adsorption layer contributes to the improvement of the corrosion resistance of the aluminum alloy coated plate, and can suppress the corrosion of the defect occurrence portion.

  As the corrosion inhibitor, as described above, one or more selected from the group consisting of benzoate, glutamate, anisidine, glycine, quinolinol, phthalate, adipate, and acetate can be used. . Among these, as a salt, alkali metal salts, such as a sodium salt and potassium salt, or ammonium salt can be used, for example. More specifically, for example, ammonium benzoate, sodium benzoate, sodium glutamate, ammonium phthalate, potassium phthalate, ammonium adipate, sodium acetate, ammonium acetate, potassium acetate and the like can be used.

The corrosion inhibitor has a hydrophobic organic chain portion and a functional group portion that is easily adsorbed on a metal surface. For this reason, the corrosion inhibitor dissolves into the water at the time of flooding, and the corrosion inhibitor is concentrated in the course of drying, and it is easy to form a hydrophobic adsorption layer on the surface of the aluminum alloy coated plate. This adsorption layer can improve the corrosion resistance. In particular, when hem processing is performed on the aluminum alloy coated plate, the joint portion of the metal plate has a bag-like structure in the processed portion, and a general electrodeposition paint does not precipitate, and the above-described penetration defects, etc. Although it is difficult to obtain an effective anticorrosion effect at the defect occurrence portion, since the resin coating layer A contains a corrosion inhibitor, the formation of the adsorption layer can improve the corrosion resistance.
Preferably, the resin coating layer A preferably contains at least a benzoate as a corrosion inhibitor. In this case, the corrosion inhibition effect can be further improved.

  When the content of the corrosion inhibitor in the resin coating layer A exceeds 25 parts by mass with respect to 100 parts by mass of the resin component, the corrosion inhibitor is formed when the resin coating layer A is formed by baking, for example. There is a risk of foaming. As a result, the adhesiveness of the resin coating layer A may be reduced, or the corrosion resistance may be reduced. Moreover, the said corrosion inhibitor can be selectively added and the content can also be made into 0 mass part. However, in order to sufficiently obtain the addition effect, the content of the corrosion inhibitor is preferably 5 parts by mass or more and more preferably 15 parts by mass or more with respect to 100 parts by mass of the resin component. .

Further, when the content of the metal powder in the resin coating layer A is a part by mass and the content of the corrosion inhibitor in the resin coating layer A is b part by mass, 0 ≦ b / a ≦ 25 is satisfied. It is preferable to satisfy (Claim 7).
In the case of b / a> 25, there is a possibility that workability at the time of hem processing and the like is lowered.

The thickness of the resin coating layer A is preferably 0.5 to 30 μm. When the thickness of the resin coating layer A is less than 0.5 μm, the corrosion inhibiting effect by the resin coating layer A may be reduced. More preferably, the resin coating layer has a thickness of 1 μm or more, and more preferably 6 μm or more. On the other hand, when it exceeds 30 μm, the adhesion between the resin coating layer A and the substrate is lowered, and there is a possibility that peeling occurs during processing. On the other hand, if the thickness of the resin coating layer A is too large, metal powder such as zinc powder is precipitated, and the resistance value of the surface of the resin coating layer A is increased, which may reduce the corrosion resistance. Further, even if the thickness is increased beyond 30 μm, the effect of inhibiting corrosion is no longer improved, and an effect commensurate with the cost cannot be obtained.

Metal powder such as zinc powder or zinc alloy powder contained in the resin coating layer A is easily dissolved in dilute acids such as hydrochloric acid and nitric acid, and is also easily dissolved in an alkaline solution. However, when the aluminum alloy coated plate having the resin coating layer A containing the metal powder is applied to, for example, a structural member, a step of degreasing with acid or alkali may be performed as a pretreatment. In this case, in the degreasing step, the metal powder contained in the resin coating layer A is eluted, and the zinc concentration of the resin coating layer A is lowered, so that a sufficient anticorrosion effect may not be obtained. Further, when zinc is completely eluted, the portion becomes a new coating film defect, which may reduce the corrosion resistance. Therefore, by providing the resin coating layer B having acid resistance and alkali resistance on the resin coating layer A, consumption of zinc in the degreasing process can be suppressed, and a desired corrosion life can be obtained. Further, the resin coating layer A formed on the surface of the substrate has coating irregularities at the time of formation and coating defects (pinholes) penetrating the resin coating layer A due to bubbles, and the resin coating layer A alone has pinholes. The effect to prevent is weak. Therefore, by further providing the resin coating layer B on the resin coating layer A, it is possible to suppress the generation of pinholes that completely penetrate the resin coating layer, and to suppress the consumption of zinc contained in the resin coating layer A. be able to.
Therefore, in the said aluminum alloy coating board, 1 or more types of resin selected from the group which consists of an epoxy-phenol resin, an epoxy- urea resin, and a polyester resin on the said resin film layer A as a main component of a resin component It is preferable that the total thickness of the resin coating layer A and the resin coating layer B is 7 to 30 μm.

  When the total thickness is less than 7 μm, the effect of preventing the formation of through holes due to multilayering may be reduced. More preferably, the total thickness of the resin coating layer A and the resin coating layer B is preferably 12 μm or more, and more preferably 15 μm or more. On the other hand, when the total thickness exceeds 30 μm, the adhesion between the resin coating layer A and the resin coating layer B and the substrate is lowered, and there is a possibility that peeling occurs during processing. Further, even if the thickness is increased beyond 30 μm, an effect commensurate with the cost cannot be obtained. More preferably, the total thickness of the resin coating layer A and the resin coating layer B is 25 μm or less.

  Further, the total thickness of the resin coating layer A and the resin coating layer B is preferably 7 to 30 μm as described above, but when the resin coating layer B is formed on the resin coating layer A, The thickness of the resin coating layer A is preferably 6 to 24 μm, and the thickness of the resin coating layer B is preferably 1 to 24 μm.

  As the epoxy-phenol resin, epoxy-urea resin, and polyester resin in the resin coating layer B, the same epoxy-phenol resin, epoxy-urea resin, and polyester resin as those in the resin coating layer A may be used. it can.

The resin coating layer B preferably contains 50 parts by mass or less of resin beads having an average particle diameter of 5 to 130 μm with respect to 100 parts by mass of the resin component in the first resin coating layer B.
In this case, for example, it is possible to prevent a flaw from being generated in the hem processing portion during hem processing.
As the resin beads, a hollow type or a solid (filled) type can be used. The hollow type is desirable from the viewpoint of high cushioning effect and high scratch prevention effect.

  If the average particle diameter of the resin beads is less than 5 μm, the above-mentioned flaw prevention effect may not be sufficiently obtained. On the other hand, when the average particle diameter exceeds 130 μm, the beads may come into contact with each other at the hem-processed portion, and the resin coating layer may be easily peeled off. The “average particle size” indicates the particle size at an integrated value of 50% in the particle size distribution obtained by the laser diffraction / scattering method.

Moreover, when content of the said resin bead exceeds 50 mass parts with respect to 100 mass parts of said resin components in the said resin coating layer B, the softness | flexibility of the said resin coating layer is lost and workability falls. There is a fear.
The resin beads are a selective component, and the content thereof may be zero. When the resin beads are added, the content is preferably 1 part by mass or more and more preferably 10 parts by mass or more in order to sufficiently obtain the effect of addition.

When the resin beads are used, the relationship between the resin beads and the thickness of the resin coating layer B is preferably 0.1 <average particle diameter of the resin beads / thickness of the resin coating layer B <12. It is preferable to be within the range.
If the ratio of the average particle diameter of the resin beads to the thickness of the resin coating layer B is 0.1 or less, the flaw prevention property of the hem-processed portion may be lowered. On the other hand, if the ratio of the average particle diameter of the resin beads to the thickness of the resin coating layer B is 12 or more, the resin beads may fall off from the resin coating layer B. More preferably, 0.1 <average particle diameter of resin beads / thickness of resin coating layer B <5 is preferable.

  Examples of the resin beads include “Matsumoto Microsphere F-36”, “Matsumoto Microsphere F-36LV”, “Matsumoto Microsphere F-48”, “Matsumoto Microsphere FN-80GS”, “Matsumoto Microsphere F-36LV”, "Matsumoto Microsphere F-50", "Matsumoto Microsphere F-65", "Matsumoto Microsphere FN-100SS", "Matsumoto Microsphere FN-100S", "Matsumoto Microsphere F-100M", "Matsumoto Microsphere FN-" 100M "," Matsumoto Microsphere FN-100 "," Matsumoto Microsphere FN-105 ", Matsumoto Microsphere FN-180SS," Matsumoto Microsphere FN-180S "," Matsumoto Microsphere FN- “80”, “Matsumoto Microsphere MFL-81GCA”, “Matsumoto Microsphere MFL-HD30CA”, “Matsumoto Microsphere MFL-HD60CA”, “Matsumoto Microsphere FN-80SDE”, “Matsumoto Microsphere F-80DE”, etc. be able to. In addition, “Gantz Pearl GM-0801”, “Gantz Pearl GM-1001”, “Gantz Pearl GM-2001”, “Gantz Pearl GM-2801”, “Gantz Pearl GM-4003”, “Gantz Pearl” of Gantz Kasei Co., Ltd. GM-5003, Gantz Pearl GB-05S, Gantz Pearl GB-08S, Gantz Pearl GB-10S, Gantz Pearl GB-15S, Gantz Pearl GB-22S, Gantz Pearl GB- 28 "," Ganz Pearl GB-55 ", etc. can also be used.

Further, the resin coating layer B per 100 parts by mass of the resin component in RESIN coating layer B, lanolin, carnauba, polyethylene, and one or more inner wax selected from microcrystalline 75 parts by weight It is preferable to contain (Claim 11).
In this case, it is possible to prevent the generation of scratches (scratches) due to contact with the mold during press working or contact during transportation. In addition, workability such as bending can be improved.

When the content of the inner wax exceeds 75 parts by mass, the amount of the inner wax deposited on the surface of the resin coating layer increases, and the wax may be easily deposited on a mold or the like during molding. More preferably, it is 50 parts by mass or less.
The inner wax is a selective component and the content thereof may be zero. In the case of adding the inner wax, the content is preferably 2 parts by mass or more, more preferably 20 parts by mass or more in order to sufficiently obtain the effect of addition. Further, two or more kinds of the above inner waxes such as carnauba and polyethylene may be mixed and used, and the mixing ratio (weight ratio) can be arbitrarily set. For example, when a mixture of carnauba and polyethylene is used, it is preferably 0: 100 to 75:25 (carnauba: polyethylene).

  When the resin coating layer B is not formed on the resin coating layer A, the resin coating layer A can contain the resin beads and / or the inner wax. In this case, the above-described preferred embodiments relating to the resin beads and the inner wax in the resin coating layer B can be similarly applied to the resin beads and the inner wax in the resin coating layer A.

  The resin coating layer A and the resin coating layer B can be formed by applying and baking a liquid paint containing the above-described blending components on the substrate.

In this example, a plurality of aluminum alloy coated plates (samples 1 to 62) according to examples and comparative examples are produced and evaluated.
As shown in FIG. 1, the aluminum alloy coated plate 1 according to the example includes a substrate 10 made of an aluminum alloy and a resin coating layer A12 mainly composed of a resin component formed on at least one surface 101 thereof. As shown in FIG. 2, the aluminum alloy coated plate 1 is used in contact with a zinc-plated or zinc-aluminum-plated steel plate 2. The resin coating layer A12 is formed on at least the contact surface 101 of the substrate 10 on the steel plate 2 side.

A chemical conversion film (not shown) is formed between the substrate 10 and the resin film layer A12.
The resin coating layer A12 contains a resin component as a main component and further contains at least zinc powder and / or zinc alloy powder as metal powder. The surface resistance (electric resistance) of the resin coating layer A12 is less than 300Ω.

  Moreover, in this example, as shown in FIG. 3, the aluminum which formed resin film layer B13 which has epoxy-phenol resin, epoxy-urea resin, or polyester resin as a main component of resin component on resin film layer A12 was further formed. An alloy coated plate 3 was produced. Further, the aluminum alloy coating plate 3 (see FIG. 4) containing the resin beads 135 in the resin coating layer B13 of the aluminum alloy coating plate 3 and the aluminum alloy coating plate (not shown) containing the inner wax in the resin coating layer B13. Also made.

Hereinafter, this example will be specifically described.
In this example, as shown in Tables 1 to 9 below, a resin coating layer A12 having various compositions is formed on a substrate 10 made of an aluminum alloy, and a resin coating layer B13 is further formed as necessary. Various types of aluminum alloy coated plates (Samples 1 to 62) were prepared.
Specifically, first, as the substrate 10, an aluminum alloy plate (material: 6083, quality: T4, plate thickness: 1.0 mm) was prepared. Next, after degreasing the substrate 10, a chemical conversion treatment was performed to form a chemical conversion film. In this example, a reactive chromate film (phosphate chromate film) was formed by phosphoric acid chromate treatment so that the chromium content was 20 mg / m ² . Specifically, the chemical conversion treatment was performed by immersing the sample in the chemical conversion treatment solution, and then dried in an atmosphere of about 100 ° C. The types of chemical conversion coatings formed on the substrate 10 are shown in Tables 1 to 6 described later.

  Next, the resin coating layer A was formed by applying and baking the coating material for the resin coating layer A including the composition shown in Tables 1 to 6 on the chemical conversion coating. The coating material for the resin coating layer A is mixed with additive components such as metal powder to the main component resin so as to have a blending ratio shown in Tables 1 to 6 below, and deionized water is used as a solvent. Made. In this example, the coating film for the resin coating layer A was applied on the chemical conversion coating formed on the substrate by the bar coating method, and was cured by heating at a temperature of 250 ° C. for 30 seconds to form the resin coating layer A. About the resin coating layer A, the kind of resin, the kind of each additive, its compounding ratio, and the thickness of the resin coating layer A are shown in Table 1-Table 6 mentioned later.

  Further, in some aluminum alloy coated plates, the resin coating layer B is formed by applying and baking the coating for the resin coating layer B including the compositions shown in Tables 7 to 9 on the resin coating layer A. did. The coating for the resin coating layer B is made by mixing additive components such as resin beads and inner wax with the main component resin so as to have the blending ratios shown in Tables 7 to 9 described later, and deionizing as a solvent. Made using water. In this example, the resin coating layer B was formed by applying a coating material for the resin coating layer B onto the resin coating layer A by a bar coating method and heating and curing at 250 ° C. for 30 seconds. For the resin coating layer B, the type of resin, the type of each additive, the blending ratio thereof, the thickness of the formed resin coating layer B, and the total thickness of the resin coating layer A and the resin coating layer B are shown in Table 7 below. To Table 9.

  In Tables 1 to 9 described later, “epoxy urea A” is an epoxy-urea resin of an epoxy resin and a butylated urea resin having an epoxy equivalent of 210 g / eq. “Epoxy urea B” is an epoxy-urea resin of an epoxy resin and a butylated urea resin having an epoxy equivalent of 135 g / eq. “Epoxy urea C” is an epoxy-urea resin having an epoxy equivalent of 145 g / eq and an epoxy resin and a butylated urea resin. “Epoxy urea D” is an epoxy-urea resin of an epoxy resin and a butylated urea resin having an epoxy equivalent of 430 g / eq. “Epoxy urea E” is an epoxy-urea resin of epoxy resin and butylated urea resin having an epoxy equivalent of 470 g / eq.

  "Epoxy-phenol A" is an epoxy-phenol resin having an epoxy equivalent of 210 g / eq and an epoxy resin and a resol type phenol resin. “Epoxy-phenol B” is an epoxy-phenol resin having an epoxy equivalent of 135 g / eq and an epoxy resin and a resol type phenol resin. “Epoxy-phenol C” is an epoxy-phenol resin having an epoxy equivalent of 145 g / eq and an epoxy resin and a resol type phenol resin. “Epoxy-phenol D” is an epoxy-phenol resin having an epoxy equivalent of 430 g / eq and an epoxy resin and a resol type phenol resin. "Epoxy-phenol E" is an epoxy-phenol resin having an epoxy equivalent of 470 g / eq and an epoxy resin and a resol type phenol resin.

  “Polyester A” is a polyester resin having a number average molecular weight of 15000, an elongation at break of 125%, and a glass transition point of 17 ° C. “Polyester B” is a polyester resin having a number average molecular weight of 3000, an elongation at break of 2%, and a glass transition point of 40 ° C. “Polyester C” is a polyester resin having a number average molecular weight of 5000, an elongation at break of 120%, and a glass transition point of 55 ° C. “Polyester D” is a polyester resin having a number average molecular weight of 16000, an elongation at break of 206%, and a glass transition point of 19 ° C. “Polyester E” is a polyester resin having a number average molecular weight of 17,000, an elongation at break of 1200%, and a glass transition point of 10 ° C.

Moreover, in this example, zinc powder, zinc alloy powder, aluminum powder, and aluminum alloy powder were used as the metal powder in the examples.
As the zinc powder, “R powder”, “F powder”, or “UF powder” manufactured by Hakusui Tech Co., Ltd. was used.
As the zinc alloy powder, “Zn-22.3Al”, “Zn-2Al”, or “Zn-50Sn” manufactured by Hikari Material Industries Co., Ltd. was used.
As aluminum powder, “# 1000F” manufactured by Minalco Co., Ltd. was used.
As the aluminum alloy powder, “Al-25Si-30Zn” manufactured by Hikari Materials Industry Co., Ltd. was used.
In the comparative examples, Sn powder, Mg powder, and Ni powder were used as the metal powder, but these were also commercially available.

Next, various performance evaluation tests were performed on the aluminum alloy coated plates of Sample 1 to Sample 62.
<Surface resistance>
As shown in FIG. 5, the aluminum alloy coated plate 1 of each sample was placed on the pedestal 8 with the painted surface on which the resin coating layer 12 was formed facing upward. Then, on the coated surface of the aluminum alloy coated plate 1, by arranging a copper plate electrode 81 formed in a length of 100 mm × width of 100 mm × thickness of 0.5 mm, and further placing a weight 82 having a mass of 1000 g on the copper plate electrode 81, The copper plate electrode 81 was brought into contact with the aluminum alloy plate 1 with a load of 1000 g. The lead wires 851 and 852 of the multimeter 85 were connected to the aluminum alloy coated plate 1 and the copper plate electrode 81, respectively, and the electrical resistance of the surface of the resin coating layer A12 of the aluminum alloy coated plate 1 was measured by the multimeter 85. The measurement was performed on arbitrary five points on the resin coating layer A12, and the average was obtained. The results are shown in Tables 10 and 11 below.
In measuring the surface resistance of the aluminum alloy coated plate 3 (see FIGS. 3 and 4) on which the resin coating layer B13 is formed on the resin coating layer A12, the resin coating layer A12 before the resin coating layer B13 is formed. The surface resistance of the resin coating layer A12 was measured in a state where only the film was formed (that is, the state shown in FIG. 1). For convenience of explanation, in FIG. 5, the aluminum alloy coated plate 3, the copper plate electrode, and the weight are shown in a sectional view, and the other configurations are shown in a side view.

<Corrosion test>
As shown in FIG. 6, a cross cut is performed on a part of the coated surface of the aluminum alloy coated plate 1 of each sample based on 7.8 (3) of JIS-K5400 (1979). Formed. The cross cut portion 4 is partially formed on the painted surface, and a region where the cross cut portion 4 is not formed is a smooth flat plate portion 5.
Next, as shown in FIG. 7, the coated surface of the resin coating layer 12 of the aluminum alloy coated plate 1 and the galvanic steel plate 2 (galvalume steel plate) are faced, and a gauze serving as a water retention layer 6 is sandwiched therebetween, and the aluminum alloy coating is performed. The plate 1 and a galvanic steel plate (galvalume steel plate) were fixed with a metal clip 65 to obtain a test piece.
About this test piece, the salt spray test based on 7.8 of JIS-K5400 (1979) was done. The temperature of the test tank was 35 ° C., the concentration of saline was 5% by mass, and the spraying time was 2 hours. Thereafter, a constant temperature and humidity test was performed. The constant temperature and humidity test was performed by leaving it in a constant temperature and humidity tester having a temperature of 50 ° C. and a humidity of 85% RH for 72 hours. A combination of the salt spray test and the constant temperature and humidity test was defined as one cycle, and each sample was repeated four cycles.
After visually observing the surface of the aluminum alloy coated plate 1 after the test, the depth of focus was measured at a magnification of 100 times with an optical microscope to obtain the corrosion depth. The corrosion depth was measured at three points in the crosscut portion 4 and at any five points in the portion where the crosscut was not made (flat plate portion 5), and the average value was obtained. The results are shown in Table 10 and Table 11.
6 and 7, the corrosion test method is illustrated for the aluminum alloy coated plate 1 on which the resin coating layer A12 is formed. However, the aluminum alloy coating on which the resin coating layer B13 is formed on the resin coating layer A12 is illustrated. The corrosion test was similarly performed on the plate 3 (see FIGS. 3 and 4).

<Coating film adhesion>
As shown in FIG. 8, the aluminum alloy coated plate 1 of each sample was folded 180 ° (0T bending) with the coated surface of the resin coating layer A12 inside, and folded 180 ° across a 1 mm thick plate ( (1T bending) and 180 ° bending (2T bending) with a plate having a thickness of 2 mm. That is, the aluminum alloy plate 1 was folded at 180 ° with the coating surface of the resin coating layer A12 on the inside so that the distance D in FIG. 8 was 0 mm, 1 mm, or 2 mm. Thereafter, the aluminum alloy coated plate 1 was filled with resin, and the state of the resin coating layer A12 was observed from the cross section. If there was no peeling of resin film A12, it was set as acceptable, and the case where peeling was observed was set as unacceptable. The results are shown in Table 10 and Table 11.
In FIG. 8, a coating adhesion test method is illustrated for the aluminum alloy coated plate 1 on which the resin coating layer A12 is formed. However, the aluminum alloy coating on which the resin coating layer B13 is formed on the resin coating layer A12 is illustrated. For the plate 3 (see FIGS. 3 and 4), the coating film adhesion test was conducted in the same manner.

<Moldability>
As shown in FIG. 9, the resin coating layer A <b> 12 is ruptured by pressing the aluminum alloy coating plate 1 of each sample partially to form a convex portion 18 protruding to the side opposite to the surface on which the resin coating layer A <b> 12 is formed. And measure the molding height at break.
Specifically, as shown in FIG. 9, the aluminum alloy coated plate 1 of each sample was held between a die 71 of the press machine 7 and a wrinkle presser 72 with a wrinkle presser load of 40 kN and restrained. The die 71 is provided with a hole 710 through which the punch 73 passes. Then, as shown in FIG. 9, the punch 73 is brought into contact with the surface of the aluminum alloy coated plate 1 on which the resin coating layer A12 is formed, and the punch 103 is pushed up into the hole 710 of the die 71, whereby the aluminum alloy coated plate 1 is made of resin. A protruding portion 18 that protrudes partially toward the coating layer forming side was formed on the aluminum alloy coated plate 1 by projecting in an inverted U shape on the side opposite to the side on which the coating layer 12 was formed. Then, the punch 73 was raised until the resin coating layer A12 of the aluminum alloy coated plate 1 was broken, and the rising height of the punch at the time of breaking was measured. The results are shown in Table 10 and Table 11. It preferably has a moldability of a molding height of 18 cm or more.
In the press working, a commercially available press working oil is applied as a lubricant to the surface on which the resin coating layer 12 is formed, and the wrinkle holding load: 40 kN, punch diameter φ50 mm, r: 25 mm, punch lifting speed: 120 mm / min. And temperature: 25 ° C.
FIG. 9 shows a formability test method for the aluminum alloy coated plate 1 on which the resin coating layer A12 is formed, but the aluminum alloy coated plate 3 on which the resin coating layer B13 is formed on the resin coating layer A12. (See FIGS. 3 and 4), a moldability test was conducted in the same manner.

<Wax accumulation>
The press work until the resin film layer in the moldability evaluation test was broken was repeated 20 times. Then, the tip of the punch 73 of the press machine 7 was observed with a magnifying glass (magnification 4 times) to check for the presence of wax accumulation. A case where no wax accumulation was observed was evaluated as acceptable, and a case where wax accumulation was observed was evaluated as unacceptable. The results are shown in Table 10 and Table 11.

<Pencil hardness>
According to the pencil scratch test specified in JIS-K5400 (1979), the pencil hardness of the resin coating layer of the aluminum alloy coated plate of each sample was measured. The results are shown in Table 10 and Table 11. The pencil hardness is preferably 2H or more.

  As is known from Tables 1 to 11, as the metal powder, aluminum containing at least zinc powder and / or zinc alloy powder and having a resin film layer A12 having a surface resistance of less than 300Ω formed on the substrate 10 made of an aluminum alloy. It can be seen that the alloy coated plate 1 (3) can sufficiently suppress the contact corrosion with the galvanized steel plate or the zinc-aluminum plated steel plate 2 (see FIGS. 1 to 4).

As shown in FIGS. 1-4, in the aluminum alloy coating board 1 (3) concerning the Example of this example, resin coating layer A12 contains zinc powder and / or zinc alloy powder as metal powder, and resin The surface resistance of the coating layer A is less than 300Ω. Therefore, the contact potential between the zinc layer (not shown) of the galvanized steel plate 2 or the zinc-aluminum plated steel plate 2 and the aluminum alloy coated plate 1 (3) can be made closer. Therefore, even if a coating film defect occurs in the resin coating layer A12, the consumption of the zinc layer of the galvanized steel sheet 2 or the zinc-aluminum plated steel sheet 2 during water exposure is suppressed, and iron is exposed. Thus, the occurrence of pitting corrosion on the substrate 10 made of aluminum or aluminum alloy can be suppressed.
Therefore, the aluminum alloy coated plate 1 (3) according to the example can sufficiently suppress the contact corrosion on the contact surface with the galvanized steel plate or the zinc-aluminum plated steel plate.

  In addition, in the aluminum alloy coated plate 3 in which the resin coating layer B13 is laminated on the resin coating layer A12, the through holes 120 and 130 (pinholes 120 and 130) that are likely to occur when the resin coating layers 12 and 13 are formed. It is possible to prevent the resin coating layers 12 and 13 from being completely penetrated (see FIGS. 3 and 4). That is, when the resin coating layers 12 and 13 are formed by, for example, a roll coater method that is widely used in industry, the coating film penetrates through the resin coating layers 12 and 13 by entrainment of bubbles in the paint or foaming when the solvent volatilizes. Defects are likely to occur. When the resin coating layer is formed by multilayering two or more coating layers of the resin coating layer A12 and the resin coating layer B13, the occurrence of penetration defects can be prevented.

  Thus, in the aluminum alloy coating board 1 (3) concerning an Example, the contact corrosion in a contact surface with the galvanized steel plate 2 or the zinc-aluminum plated steel plate 2 can fully be suppressed.

1 Aluminum alloy coated plate 10 Substrate 12 Resin coating layer A
13 Resin coating layer B

Claims (12)

An aluminum alloy coated plate used in contact with a galvanized steel plate or a zinc-aluminum plated steel plate,
The aluminum alloy coated plate has a substrate made of aluminum or an aluminum alloy, and a resin coating layer A containing a resin component and metal powder formed on at least the contact surface on the steel plate side of the substrate,
The resin coating layer A contains a zinc powder and / or a zinc alloy powder as the metal powder, and has a surface resistance of less than 300Ω.   2. The aluminum alloy coated plate according to claim 1, wherein the resin coating layer A contains 1 to 300 parts by mass of the metal powder with respect to 100 parts by mass of the resin component.   3. The aluminum alloy coated plate according to claim 1, wherein the resin coating layer A comprises the zinc powder as a main component of the metal powder.   3. The aluminum alloy coated plate according to claim 1, wherein the resin coating layer A comprises the zinc alloy powder as a main component of the metal powder.   The aluminum alloy coated plate according to any one of claims 1 to 4, wherein the resin coating layer A further contains an aluminum powder and / or an aluminum alloy powder as the metal powder. Painted board.   In the aluminum alloy coating plate as described in any one of Claims 1-5, the said resin coating layer A is a benzoate, glutamate, anisidine, glycine, quinolinol, phthalate with respect to 100 mass parts of said resin components. An aluminum alloy coated plate comprising 25 parts by mass or less of one or more kinds of corrosion inhibitors selected from the group consisting of acid salts, adipates, and acetates.   The aluminum alloy coated plate according to claim 6, wherein the content of the metal powder in the resin coating layer A is a part by mass, and the content of the corrosion inhibitor in the resin coating layer A is b part by mass. Then, the aluminum alloy coating plate characterized by satisfying 0 ≦ b / a ≦ 25.   The aluminum alloy coated plate according to any one of claims 1 to 7, wherein the resin coating layer A is one or more selected from the group consisting of an epoxy-phenol resin, an epoxy-urea resin, and a polyester resin. An aluminum alloy coated plate comprising a resin as a main component of the resin component.   The aluminum alloy coated plate according to any one of claims 1 to 8, wherein one or more selected from the group consisting of an epoxy-phenol resin, an epoxy-urea resin, and a polyester resin on the resin coating layer A. An aluminum alloy coated plate having a resin coating layer B containing the above resin as a main component of a resin component, wherein the total thickness of the resin coating layer A and the resin coating layer B is 7 to 30 μm.   10. The aluminum alloy coated plate according to claim 9, wherein the resin coating layer B contains 50 parts by mass of resin beads having an average particle diameter of 5 to 130 μm with respect to 100 parts by mass of the resin component in the first resin coating layer B. An aluminum alloy coated plate characterized by containing:   The aluminum alloy coated plate according to any one of claims 1 to 10, wherein the resin coating layer B is lanolin, carnauba, polyethylene, 100 parts by mass of the resin component in the first resin coating layer B. And 75 parts by mass or less of one or more types of inner wax selected from microcrystalline.   The aluminum alloy coated plate according to any one of claims 1 to 11 is used by being mechanically or chemically bonded to the unpainted galvanized steel plate or the zinc-aluminum plated steel plate. Aluminum alloy coated plate.

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