JP6218719B2 - Aluminum fin material - Google Patents

Description

  The present invention relates to an aluminum fin material used for a heat exchanger or the like.

  With the recent emergence of global warming and the problem of soaring resource prices, there is an increasing demand for performance improvements such as higher efficiency and downsizing of air conditioners. Reflecting these demands, fins formed using aluminum plates (including aluminum alloy plates) with excellent thermal conductivity, workability, corrosion resistance, etc. are widely used in heat exchangers for air conditioners. . In addition, the heat exchanger of the air conditioner has a structure in which the fins are provided in parallel at a narrow interval in order to reduce the volume.

  If the temperature of the fin surface becomes below the dew point of air during the operation of the air conditioner, the condensed water will condense and adhere to the fin surface, and the heat exchange function of the heat exchanger will deteriorate. Also, at this time, if the fin surface has low hydrophilicity, the contact angle of water becomes large, so the attached condensed water becomes hemispherical water droplets, and the height to the top of the water droplets becomes high, so the fins are blocked with condensed water. It becomes easy to do. When condensation of the condensed water further proceeds and water droplets due to the condensed water increase, the condensed water on the adjacent fin surfaces is combined, and the adjacent fins and the fins are blocked by the condensed water. When the fins are blocked by the dew condensation water in this way, a problem that the heat exchange function of the heat exchanger is further deteriorated and a problem that the dew condensation water is scattered outside the air conditioner by the wind pressure of the blower fan are conventionally known. ing.

The invention which solves the problem of the dew condensation water is disclosed in Patent Documents 1 to 6, for example.
Specifically, Patent Document 1 discloses that 5 to 25 parts by mass of sodium salt and / or potassium salt of carboxymethyl cellulose, 25 to 50 parts by mass of ammonium salt of carboxymethyl cellulose, and N-methylolacrylamide 25 in terms of solid content. Hydrophilic surface treatment containing 1.5 to 15 parts by mass of polyacrylic acid and 0.6 to 9 parts by mass (as Zr) of a zirconium compound with respect to 100 parts by mass in total of components consisting of ~ 70 parts by mass Agents are disclosed.

  Patent Document 2 discloses a hydrophilized surface treatment agent for aluminum heat exchangers, which is (a) a polyvinyl alcohol having a saponification degree of 98% or more and a polymerization degree of 150 to 350 in terms of solid content of 40 to 60 mass. And (b) a polyvinyl pyrrolidone having a polymerization degree of 15 to 40 and a polyvinyl pyrrolidone having a polymerization degree of 100 to 300 at a mass ratio of 1: 1.5 to 1: 3.0, and a total of 20 A water-soluble resin containing ˜40 parts by mass, (c) 10-20 parts by mass of water-soluble nylon, (d) 2-12 parts by mass of water-soluble phenol resin, and (e) a nonionic surfactant. 1 to 10 parts by mass with respect to 100 parts by mass of the water-soluble resin, and 5 to 20 parts by mass of (f) bis (2-pyridylthio) -zinc-1,1-dioxide with respect to 100 parts by mass of the water-soluble resin. Hydrophilic table containing parts Processing agent is disclosed.

In Patent Document 3, at least one of a corrosion-resistant film and a hydrophilic film is provided on at least one surface of an aluminum plate or an aluminum alloy plate, and an organic crosslinking agent is added to a water-soluble polyether polyol compound. A hydrophilic surface-treated fin material having a slow-eluting lubricating film composed of an organic resin crosslinked by using the slow-eluting lubricating film, the coating amount of the slow-eluting lubricating film being 50 to 500 mg / m ^2. Heat having a friction coefficient of 0.15 or less when pure water is applied on the film and a contact angle θ of water droplets of 30 ° or less generated when pure water is dropped on the slow-eluting lubricating film A hydrophilic surface treatment fin material for an exchanger is disclosed.

  In Patent Document 4, a substrate made of aluminum or an aluminum alloy, a corrosion-resistant film made of an inorganic oxide or an organic-inorganic composite compound formed on the substrate, and a film thickness of 0 formed on the corrosion-resistant film are disclosed. In an aluminum fin material provided with a resin corrosion resistant film of 5 to 10 μm and a hydrophilic film of 0.1 to 10 μm thick made of a hydrophilic resin formed on the resin corrosion resistant film, the resin corrosion resistant film includes: It is a resin comprising at least one of a urethane resin, an epoxy resin, a polyester resin, and a vinyl chloride resin, and zinc pyrithione having an average particle diameter of 0.01 to 1.0 μm with respect to 100 parts by mass of the resin. An aluminum fin material containing 0.1 to 100 parts by mass is disclosed.

  Patent Document 5 discloses a substrate made of aluminum or an aluminum alloy, a base treatment layer made of an inorganic oxide or an organic-inorganic composite compound formed on the substrate, and a film formed on the base treatment layer. In an aluminum fin material for a heat exchanger comprising a hydrophobic coating layer having a thickness of 0.1 to 10 μm and a hydrophilic coating layer having a thickness of 0.1 to 10 μm formed on the hydrophobic coating layer, The hydrophobic coating layer is made of at least one hydrophobic resin of urethane resin, epoxy resin, polyester resin and polyacrylic acid resin, and the hydrophilic coating layer is a sulfonic acid group or It comprises a hydrophilic resin containing a sulfonic acid group derivative and containing at least one of a carboxyl group, a carboxyl group derivative, a hydroxyl group and a hydroxyl group derivative. -The abundance ratio of S measured in the film thickness direction by discharge emission spectroscopic analysis is 1 to 5 atomic% and the abundance ratio of O is 10 to 35 atomic%, and the hydrophobic coating layer and the hydrophilic coating layer An aluminum fin material for a heat exchanger is disclosed in which the total amount of at least one of alumina, silica, titania, zeolite and hydrates contained as impurities in the film layer is 1% by mass or less.

  Patent Document 6 discloses an aluminum fin material provided with a corrosion-resistant film layer and a hydrophilic film layer in this order on the surface of an aluminum plate or an aluminum alloy plate, and the corrosion-resistant film layer includes a polyester resin, a polyolefin-based material. One or more corrosion-resistant resins selected from the group consisting of resins, epoxy resins, acrylic resins, and urethane resins, water-soluble epoxy resins, water-soluble carbodiimide compounds, water-dispersible carbodiimide compounds, and water-soluble One or more first cross-linking agents selected from the group consisting of oxazoline group-containing resins, and the solid content ratio of the first cross-linking agent in the total solid content of the corrosion-resistant resin and the first cross-linking agent is Polymerization comprising a resin composition of 0.2% or more, wherein the hydrophilic film layer is composed only of a monomer having a carboxyl group As well as copolymers containing a monomer having a carboxyl group, or an aluminum fin material made of a resin composition including mixtures thereof is disclosed.

Japanese Patent No. 2520308 Japanese Patent No. 2574197 Japanese Patent No. 4164049 Japanese Patent No. 4456551 JP 2008-224204 A JP2013-190178A

  However, in any of the inventions disclosed in Patent Documents 1 to 5, when the hydrophilic resin film comes into contact with water, the hydrophilicity decreases with time, and it is difficult to maintain the hydrophilicity of the fin surface over a long period of time. Also in Patent Document 6, when various suspended substances adhere, deterioration of hydrophilicity with time and promotion of corrosion of the fin material and the copper tube occur.

  This invention is made | formed in view of the said problem, and makes it a subject to provide the fin material made from aluminum in which the hydrophilic property of the fin material surface lasts for a long period of time.

An aluminum fin material according to the present invention that has solved the above-mentioned problems is provided with a base treatment layer made of an inorganic oxide or an inorganic-organic composite compound on the surface of a plate made of aluminum or an aluminum alloy, and a corrosion-resistant coating layer (however, the corrosion-resistant coating) An aluminum fin material provided with a hydrophilic coating layer in this order, excluding those comprising a resin composition in which the solid content ratio of the crosslinking agent in the solid content of the layer is 0.2% by mass or more, The corrosion-resistant film layer is made of a resin composition containing a corrosion-resistant resin made of a resin having an acrylic resin structure, and the hydrophilic film layer is one or more functional groups selected from a sulfonic acid group and an alkali metal base of sulfonic acid. Resin composition comprising at least one of a monomer having a group, a polymer composed only of the monomer, and a copolymer containing the monomer Rannahli, and, the hydrophilic film layer formed to not more than 30 degrees contact angle with pure water immediately after returning to room temperature, and the structure surface area of not more than 5%.

  With such a configuration, the aluminum fin material according to the present invention is a corrosion-resistant film made of a sulfone-based hydrophilic resin that easily elutes with moisture such as condensed water while maintaining the corrosion resistance of the corrosion-resistant resin. It becomes possible to maintain hydrophilicity by tying the layers. For this reason, the aluminum fin material according to the present invention is less likely to have a good contact angle with water of 30 degrees or less at the initial stage (immediately after forming the hydrophilic coating layer). In addition, since the surface area ratio of the hydrophilic film layer is 5% or less, the aluminum fin material according to the present invention has few adsorption sites for suspended solids, and promotes corrosion reduction by adsorbing contaminants and reducing hydrophilicity due to adhering contaminants. Can be suppressed.

In the aluminum fin material according to the present invention, the corrosion-resistant coating layer contains a corrosion-resistant resin matrix and an antibacterial agent, and the adhesion amount of the corrosion-resistant resin matrix is 0.01 to 8.0 g / m ^2. Contains at least one of Zn and Ag, and satisfies at least one of 0.1 to 40% by mass of Zn and 0.001 to 1.0% by mass of Ag with respect to the corrosion-resistant resin matrix, and contains The total of the Zn content and the Ag content is preferably 41% by mass or less.
With such a configuration, the aluminum fin material according to the present invention is excellent in corrosion resistance and has a high residual ratio of the antibacterial agent, and can prevent the generation of unpleasant odor due to soot and bacteria.

The aluminum fin material according to the present invention further includes a lubricating coating layer on the hydrophilic coating layer, and the lubricating coating layer is made of polyethylene glycol, modified polyethylene glycol, carboxymethyl cellulose, and an alkali metal salt of carboxymethyl cellulose. It is preferable to consist of a resin composition containing one or more lubricating resins selected from the group.
With such a configuration, the aluminum fin material according to the present invention can obtain lubricity while maintaining the hydrophilicity of the hydrophilic coating layer.

The aluminum fin material according to the present invention preferably has an adhesion amount of the lubricating coating layer of 0.01 to 0.8 g / m ² .
With such a configuration, the aluminum fin material according to the present invention can obtain lubricity and suppress color unevenness due to discoloration at the time of elution of the lubricating film due to adhesion of moisture and press oil. Therefore, the designability of the aluminum fin material according to the present invention can be improved.

In the aluminum fin material according to the present invention, the total adhesion amount of each coating layer formed on the surface of the plate material is preferably 0.1 to 10.0 g / m ² per side.
If it is set as such a structure, the aluminum fin material which concerns on this invention can ensure reliably the effect anticipated for each membrane | film | coat layer.

  Since the aluminum fin material according to the present invention has the above-described configuration, the hydrophilicity of the fin material surface can be maintained for a long period of time.

It is a conceptual sectional view explaining composition of an aluminum fin material concerning one embodiment of the present invention. It is a conceptual sectional view explaining composition of an aluminum fin material concerning other embodiments of the present invention.

  Hereinafter, a form (embodiment) for carrying out an aluminum fin material according to the present invention will be described in detail with reference to the drawings as appropriate.

(One Embodiment of Aluminum Fin Material)
As shown in FIG. 1, an aluminum fin material 1 according to an embodiment of the present invention includes a base treatment layer 3 made of an inorganic oxide or an inorganic-organic composite compound, and a corrosion-resistant coating layer 4 on the surface of a plate material 2. The hydrophilic film layer 5 is provided in this order.

(Plate material)
The plate material 2 is made of aluminum or an aluminum alloy. Since the thermal conductivity and workability are excellent, 1000 series aluminum defined in JIS H 4000: 2006 can be suitably used. More specifically, aluminum with alloy numbers 1050, 1070, and 1200 can be suitably used. In addition, the above-described base treatment layer 3, the corrosion-resistant coating layer 4, and the hydrophilic coating layer 5 are formed without any problem on a plate material formed of a 2000-9000 series aluminum alloy defined in JIS H 4000: 2006. be able to. Therefore, the board | plate material 2 may be formed with the 2000 series-9000 series aluminum alloy.

  In addition, it is preferable that the board | plate material 2 shall be about 0.08-0.3 mm in thickness considering the intensity | strength, heat conductivity, workability, etc. as a fin material for heat exchangers, for example. In addition, the board | plate material 2 can be made into arbitrary board thickness by well-known methods, such as casting, hot rolling, cold rolling, and tempering.

(Undercoat layer)
The base treatment layer 3 is made of an inorganic oxide or an inorganic-organic composite compound. By forming the base treatment layer 3 on the surface of the plate material 2, the adhesion between the plate material 2 and the corrosion-resistant coating layer 4 can be improved. Moreover, the contact of the condensed water (condensation water) to the board | plate material 2 can be suppressed by forming the base-treatment layer 3 in the surface of the board | plate material 2. FIG. Therefore, when the ground treatment layer 3 is formed on the surface of the plate material 2, the corrosion resistance as the fin material can be improved.

  The inorganic oxide preferably contains Cr or Zr as a main component. Specific examples of such inorganic oxides include those formed by performing a phosphoric acid chromate treatment, a zirconium phosphate treatment, and a chromate chromate treatment. Needless to say, the inorganic oxide that can be used in the present invention is not limited to these as long as it exhibits corrosion resistance. As the inorganic oxide, in addition to those described above, for example, those formed by performing zinc phosphate treatment or phosphoric acid titanate treatment can also be used.

  Examples of the inorganic-organic composite compound include those formed by coating-type chromate treatment or coating-type zirconium treatment. Specific examples of such inorganic-organic composite compounds include acrylic-zirconium composites.

The formation of the ground treatment layer 3 can be performed, for example, by applying a chemical conversion treatment liquid to the surface of the plate material 2 by spraying or the like.
Surface treatment layer 3, for example, preferably contain Cr or Zr in the range of 1 to 100 mg / m ^2, and more preferably contains in the range of 5-80 mg / m ^2.
In addition, the thickness of the base treatment layer 3 is preferably 10 to 1000 mm, and more preferably 50 to 800 mm, but can be appropriately changed according to the purpose of use and the like.

(Corrosion-resistant coating layer)
The corrosion-resistant film layer 4 is formed between the base treatment layer 3 and a hydrophilic film layer 5 described later, thereby improving the corrosion resistance as a fin material. That is, the durability as a heat exchanger can be enhanced by forming the corrosion-resistant coating layer 4. Moreover, since the corrosion-resistant film layer 4 is hydrophobic, water can penetrate to the plate material 2 and odor caused by the occurrence of sub-film corrosion can be suppressed.

  The corrosion-resistant coating layer 4 is made of a resin composition (corrosion-resistant coating layer coating) containing a corrosion-resistant resin made of a resin having an acrylic resin structure. The resin having an acrylic resin structure refers to one or more resins selected from the group consisting of an acrylic resin having an acrylic structure and a cross-linked acrylic resin. The cross-linked acrylic resin refers to an acrylic resin having a cross-linkable functional group in the structure. Examples of the crosslinkable functional group include an isocyanate group, an epoxy group, an oxazoline group, a methylene group, a carbodiimide group, an aziridine group, and a melamine group.

The thickness (adhesion amount) of the corrosion-resistant coating layer 4 is preferably 0.01 to 8.0 g / m ² , for example. When the thickness of the corrosion-resistant coating layer 4 is within this range, the corrosion resistance as the fin material can be ensured more reliably and the adhesion with the hydrophilic coating layer 5 can be secured. Moreover, since the thickness is not so thick when the thickness of the corrosion-resistant film layer 4 is in this range, it is possible to prevent a situation where the corrosion-resistant film layer 4 becomes a heat insulating layer and deteriorates the efficiency of heat exchange. In addition, as for the thickness of the corrosion-resistant membrane | film | coat layer 4, it is more preferable to set it as 0.03-5.0 g / m < ² >, for example.

  In addition to the resin having the acrylic resin structure described above, the corrosion-resistant film layer 4 is obtained by adding various aqueous solvents and paint additives for improving the paintability, workability, and coating film properties to the resin composition. It may be formed. Examples of water-based solvents and paint additives include water-soluble organic solvents, crosslinking agents, surfactants, surface conditioners, wetting and dispersing agents, anti-settling agents, antioxidants, antifoaming agents, antirust agents, antibacterial agents, Various solvents and additives such as anti-fungal agents can be mentioned. One of these water-based solvents and paint additives can be selected from the above-described materials and blended in the resin composition, or a plurality of these can be selected and blended in the resin composition.

(Antimicrobial agent)
In the present invention, the corrosion-resistant coating layer 4 described above preferably contains an antibacterial agent. That is, the corrosion resistant coating layer 4 preferably contains a corrosion resistant resin matrix and an antibacterial agent. In this case, the adhesion amount of the corrosion-resistant coating layer 4 (corrosion-resistant resin matrix) is preferably 0.01 to 8.0 g / m ² . In this case, the antibacterial agent includes at least one of Zn and Ag, and at least 0.1 to 40% by mass of Zn and 0.001 to 1.0% by mass of Ag with respect to the corrosion-resistant resin matrix. It is preferable that the total content of Zn and Ag contained is 41% by mass or less.
By using such a corrosion-resistant coating layer 4, antibacterial properties can be imparted to the fin material, and it is possible to prevent the generation of unpleasant odor due to the propagation of soot and bacteria on the dust material or dust attached to the surface of the fin material. Can do. Moreover, the loss by the dew condensation water of an air conditioner can be avoided by containing zinc or a zinc compound, or silver or a silver compound in the hydrophobic corrosion-resistant film layer 4.

As described above, the adhesion amount of the corrosion-resistant coating layer 4 (corrosion-resistant resin matrix) when an antibacterial agent is contained is preferably 0.01 to 8.0 g / m ² . The reason why the adhesion amount of the corrosion-resistant resin matrix in this case is preferably in the above range is the same as in the case where no antibacterial agent is contained, and thus the description thereof is omitted.

  In addition, that the antibacterial agent contains one or more selected from Zn and Ag includes the case where the antibacterial agent consists of one or more selected from Zn and Ag.

  Examples of Zn include metallic zinc and zinc compounds (sometimes referred to as zinc antibacterial agents). Examples of Ag include silver metal and silver compounds (these may be referred to as silver antibacterial agents). Metal zinc or a zinc compound, or metal silver or a silver compound has a strong antibacterial action by generating zinc ions or silver ions. By containing it in the corrosion-resistant coating layer 4, the fin material is antibacterial. It is possible to prevent the generation of unpleasant odor due to the propagation of soot and bacteria on the dust or dust attached to the surface of the fin material. Moreover, the loss by the dew condensation water of an air conditioner can be avoided by containing zinc or a zinc compound, or silver or a silver compound in the hydrophobic corrosion-resistant film layer 4.

Examples of the zinc-based antibacterial agent include bis (2-pyridylthio-1-oxide) zinc, zinc-supporting zeolite, zinc-containing alloy, and the like, among these, bis (2-pyridylthio-1-oxide) Zinc is preferred.
The content of the zinc antibacterial agent in the corrosion-resistant coating layer 4 is preferably 0.1 to 40% by mass with respect to the solid content of the corrosion-resistant coating layer 4. When the content of the zinc-based antibacterial agent with respect to the solid content of the corrosion-resistant coating layer 4 is within this range, antibacterial properties can be reliably imparted to the fin material.

Examples of the silver-based antibacterial agent include silver carbonate, silver nitrate, silver oxide, silver chloride, and silver sulfate. Among these, for reasons of stability and antibacterial activity in the paint for the corrosion-resistant coating layer 4, Silver oxide is preferred.
The content of the silver antibacterial agent in the corrosion resistant coating layer 4 is preferably 0.001 to 1.0% by mass with respect to the solid content of the corrosion resistant coating layer 4. When the content of the silver-based antibacterial agent with respect to the solid content of the corrosion-resistant coating layer 4 is within this range, antibacterial properties can be reliably imparted to the fin material.

  When an antibacterial agent contains 1 or more types of Zn and Ag, as above-mentioned, it is preferable that the sum total of content of Zn to contain and content of Ag is 41 mass% or less. Thus, when the total content of Zn and Ag is 41% by mass or less, the antibacterial agent has a high residual rate and prevents the generation of unpleasant odors caused by sputum and bacteria. can do. In addition, the lower limit of the total amount of Zn content and Ag content is 0.001% by mass. When the total amount exceeds 40% by mass, both Zn and Ag are added.

(Hydrophilic film layer)
The hydrophilic coating layer 5 is composed of a monomer having one or more functional groups selected from a sulfonic acid group and an alkali metal base of sulfonic acid, a polymer composed only of the above-described monomer, and the above-described single monomer. It consists of a resin composition (coating for hydrophilic film layer) containing at least one of the copolymers containing a body. That is, the hydrophilic film layer 5 is not particularly limited as long as it contains at least a monomer having a sulfonic acid group or an alkali metal base of sulfonic acid in the side chain. The alkali metal base of sulfonic acid refers to a sulfonic acid group in which part or all of H of the molecule is an alkali metal salt (H is substituted with an alkali metal). Examples of the alkali metal salt include lithium salt, sodium salt, potassium salt and the like. The monomeric sulfonic acid group and the alkali metal base of the sulfonic acid contained in the hydrophilic coating layer 5 react with the functional groups on the surface of the corrosion-resistant coating layer 4 when the hydrophilic coating layer 5 is formed. Thereby, the adhesiveness of the corrosion-resistant film layer 4 and the hydrophilic film layer 5 is further improved, and the hydrophilic durability of the aluminum fin material according to the present invention can be improved.

The polymer composed only of the above-described monomer is obtained by polymerizing only the above-described monomer. An example of such a polymer is ATBS manufactured by Toagosei Co., Ltd.
Moreover, the copolymer containing the monomer which has an above described functional group is copolymerized using an above described monomer and a monomer different from this. Such different monomers include a monomer having a carboxyl group, a monomer having a sulfonic acid group derivative, a monomer having a carboxyl group derivative, a monomer having a hydroxyl group, and a monomer having a hydroxyl group derivative And monomers having a hydrophilic functional group such as a body. Examples of the copolymer containing a monomer having a functional group described above include AQUALIC GL manufactured by Nippon Shokubai Co., Ltd., which is a copolymer of acrylic acid and a monomer having a sulfonic acid group.

The hydrophilic coating layer 5 has a contact angle with water of 30 degrees or less immediately after forming the hydrophilic coating layer 5 (that is, at the initial stage of forming the hydrophilic coating layer 5). If the contact angle with water at the initial stage of forming the hydrophilic coating layer 5 is 30 degrees or less, even if there is a decrease in hydrophilicity over time after long-term use, sufficient hydrophilicity can be maintained. Is possible. On the other hand, if the contact angle with water in the initial stage of forming the hydrophilic coating layer 5 exceeds 30 degrees, sufficient hydrophilicity cannot be maintained when there is a decrease in hydrophilicity over time. The contact angle can be adjusted by, for example, increasing or decreasing the number of sulfonic acid groups.
The contact angle can be determined, for example, by dropping about 0.5 μL of pure water onto the surface and measuring it using a contact angle measuring instrument or the like.

Further, the surface area ratio of the hydrophilic film layer 5 is set to 5% or less. That is, the hydrophilic film layer 5 has a smooth surface with few irregularities. If the surface area ratio of the hydrophilic coating layer 5 is 5% or less, various suspended substances are difficult to adhere, and thus it is possible to prevent a decrease in hydrophilicity over time. On the other hand, when the surface area ratio of the hydrophilic coating layer 5 exceeds 5%, various suspended substances are likely to adhere, and thus the hydrophilicity deterioration with time becomes remarkable. In addition, the surface area ratio in this specification means the ratio of the surface area which has arisen with the area of the designated area | region, and the surface shape of a target object. The surface area ratio can be adjusted, for example, by not using a drug with a rough surface or by reducing the amount used.
The surface area ratio can be obtained, for example, by three-dimensionally measuring the surface of a dry sample using an atomic force microscope or a three-dimensional measuring instrument. Specifically, for example, the ratio between the surface area of the designated region (designated region surface area) and the surface area generated by the surface shape of the object (surface area of the object) may be obtained (see the following formula (1)). ).
[Formula (1)]
Surface area ratio (%) = {(surface area of target object−designated area surface area) / designated area surface area} × 100

The thickness (adhesion amount) of the hydrophilic film layer 5 is preferably 0.02 to 10 g / m ² , for example. When the thickness of the hydrophilic film layer 5 is within this range, it is possible to make it difficult to lower the hydrophilicity as the fin material. In addition, although it is more preferable that the thickness of the hydrophilic membrane | film layer 5 shall be 0.1-2 g / m < ² >, for example, it is not limited to these ranges.

  The resin composition of the hydrophilic film layer 5 is for improving paintability, workability, or coating film physical properties in addition to at least one of the aforementioned monomer, polymer, and copolymer. Various aqueous solvents and paint additives can be added. For example, various solvents such as water-soluble organic solvents, surfactants, surface conditioners, wetting and dispersing agents, crosslinking agents, anti-settling agents, antioxidants, antifoaming agents, rust inhibitors, antibacterial agents, and antifungal agents, Additives can be added alone or in combination.

  Further, the hydrophilic film layer 5 may contain a chemical for imparting other additional characteristics such as lubricity, paintability and appearance to the coating film. Examples of the agent (lubricating component) that imparts lubricity include inner waxes such as animal waxes such as lanolin, plant waxes such as carnauba, synthetic waxes such as polyethylene wax, and petroleum waxes. As the lubricating component, one or more of these can be selected and used. When a hydrophilic component is contained in the hydrophilic film layer 5, for example, the lubricity film layer 6 (see FIG. 2; the lubricity film layer 6 will be described later) is formed with good press workability without being formed. It becomes possible to do.

The total adhesion amount of the corrosion-resistant coating layer 4 and the hydrophilic coating layer 5 is preferably 0.1 to 10.0 g / m ² per side of the plate material 2, for example. If the total adhesion amount of the corrosion-resistant coating layer 4 and the hydrophilic coating layer 5 is within this range, the effects expected of each coating layer can be sufficiently expressed, and each coating layer can be formed uniformly. Easy. If the total adhesion amount of the corrosion-resistant coating layer 4 and the hydrophilic coating layer 5 is in this range, it is difficult for each coating layer to fall off during press molding, so that it is possible to improve workability. Furthermore, if the total adhesion amount of the corrosion-resistant coating layer 4 and the hydrophilic coating layer 5 is within this range, the coating layer becomes a heat insulating layer when using the air conditioner, and the heat exchange efficiency is not deteriorated. The thicknesses of the corrosion-resistant coating layer 4 and the hydrophilic coating layer 5 can be adjusted by appropriately adjusting the physical properties (viscosity) and concentration of the coating material and the coating speed with a coater.

  According to the aluminum fin material 1 according to the present embodiment described above, the predetermined base treatment layer 3, the corrosion-resistant coating layer 4, and the hydrophilic coating layer 5 are provided in this order. The hydrophilicity of the material surface can be maintained for a long time.

(Another embodiment of aluminum fin material)
Next, an aluminum fin material according to another embodiment of the present invention will be described with reference to FIG.
As shown in FIG. 2, an aluminum fin material 1 </ b> A according to another embodiment is different from the aluminum fin material 1 described with reference to FIG. 1 in that a lubricating coating layer 6 is provided. But the other elements are exactly the same. Below, the description about the same element is abbreviate | omitted and the lubricating film layer 6 which is a different element is demonstrated.

(Lubricating film layer)
The lubricating coating layer 6 is eluted in the dew condensation water adhering to the surface of the aluminum fin material 1A during operation of the heat exchanger, and the molding oil remaining on the surface of the fin material 1A is washed away with the dew condensation water. Therefore, the aluminum fin material 1A can suppress a decrease in hydrophilic sustainability caused by molding oil or the like. Further, by forming the lubricating coating layer 6 on the surface of the aluminum fin material 1A, it is possible to suppress adhesion with the mold that occurs when the fin material 1A is molded. Therefore, the aluminum fin material 1A can improve the workability.

The lubricating coating layer 6 is a resin composition containing one or more lubricating resins selected from the group consisting of resins eluting in water, for example, polyethylene glycol, modified polyethylene glycol, carboxymethyl cellulose, and alkali metal salts of carboxymethyl cellulose. Consists of.
The film thickness of the lubricating film layer 6 is preferably 0.01 to 0.8 g / m ² , for example, and more preferably 0.02 to 0.4 g / m ² . When the film thickness of the lubricating film layer 6 is within this range, the workability can be reliably improved. The formation of the lubricating coating layer 6 can be performed by applying an aqueous solution of a resin eluting into water onto the hydrophilic coating layer 5 and baking it.

Moreover, the total adhesion amount of the corrosion-resistant coating layer 4, the hydrophilic coating layer 5 and the lubricating coating layer 6 in the aluminum fin material 1A is, for example, 0.1 to 10.0 g / m ² per one side of the plate material 2. Is preferred. If the total adhesion amount of the corrosion-resistant coating layer 4, the hydrophilic coating layer 5 and the lubricating coating layer 6 is within this range, the effects expected of each coating layer can be sufficiently expressed, and each coating layer It is easy to form uniformly. Further, if the total adhesion amount of the corrosion-resistant coating layer 4, the hydrophilic coating layer 5 and the lubricating coating layer 6 is within this range, it is difficult for each coating layer to fall off during press molding, so that workability can be improved. Is possible. Furthermore, if the total adhesion amount of the corrosion-resistant coating layer 4, the hydrophilic coating layer 5 and the lubricating coating layer 6 is within this range, the coating layer becomes a heat insulating layer when using the air conditioner, and the heat exchange efficiency is deteriorated. There is no such thing. The thickness of the lubricating coating layer 6 can be adjusted by appropriately adjusting the physical properties (viscosity) and concentration of the coating for the lubricating coating layer and the coating speed by the coater.

(Method of manufacturing aluminum fin material)
Next, an example of the manufacturing method of the aluminum fin material 1 will be described. The aluminum fin material 1 can be manufactured by performing the following (1) to (3).

(1) The base treatment layer 3 made of an inorganic oxide or an inorganic-organic composite compound is formed by subjecting the surface of the plate 2 made of aluminum or an aluminum alloy to a phosphate chromate treatment, a zirconium phosphate treatment, or the like. Here, the phosphoric acid chromate treatment, the zirconium phosphate treatment, and the like are performed by applying a chemical conversion treatment liquid to the plate member 2 by spraying or the like. The coating amount is preferably 1 to 100 mg / m ^{2 in} terms of Cr or Zr, and the formed film thickness is preferably 10 to 1000 mm. Further, before forming the base treatment layer 3, it is preferable to degrease the surface of the plate material 2 in advance by spraying an alkaline aqueous solution on the surface of the plate material 2. The adhesion between the plate material 2 and the base treatment layer 3 is improved by degreasing.

(2) An aqueous solution of a corrosion-resistant resin (resin composition (coating) for the corrosion-resistant coating layer 4) is applied to the surface of the formed base treatment layer 3, and then baked to form the corrosion-resistant coating layer 4. The application method of the resin composition for the corrosion-resistant film layer 4 can be performed by a conventionally known application method such as a bar coater or a roll coater. The coating amount of the resin composition for the corrosion-resistant coating layer 4 is appropriately set (adjusted) so that the thickness (attachment amount) of the corrosion-resistant coating layer 4 is 0.01 to 8 g / m ² . Moreover, although the baking temperature (attainment temperature of the board | plate material 2) at the time of formation of the corrosion-resistant film layer 4 is suitably set with the corrosion-resistant resin to apply | coat, it is generally performed in the range of 100-300 degreeC. In addition, what is necessary is just to add an antibacterial agent to the resin composition for the corrosion-resistant film layer 4 so that it may become above-described conditions when an antibacterial agent is included in the corrosion-resistant film layer 4.

(3) On the surface of the formed corrosion-resistant coating layer 3, a polymer composed only of a monomer having one or more functional groups selected from sulfonic acid groups and alkali metal bases of sulfonic acid groups, and After applying an aqueous solution (resin composition for hydrophilic film layer 5 (paint)) containing at least one of the copolymers containing the monomers, baking is performed to form hydrophilic film layer 5. The fin material 1 is made of aluminum. The application method of the resin composition for the hydrophilic film layer 5 can be performed by a conventionally known application method such as a bar coater or a roll coater. The application amount of the resin composition for the hydrophilic film layer 5 is appropriately set (adjusted) so that the thickness (adhesion amount) of the hydrophilic film layer 5 is 0.02 to 10 g / m ² . Moreover, although the baking temperature (attainment temperature of the board | plate material 2) at the time of hydrophilic membrane layer 5 formation is suitably set with the resin composition for hydrophilic membrane layers 5 to apply | coat, it carries out in the range of 150-300 degreeC as above-mentioned. Is preferred.

Moreover, after performing said (1)-(3), 1A of aluminum fin materials can be manufactured by performing the following (4).
(4) An aqueous solution of a resin (water-soluble resin) that easily dissolves in water (resin composition (paint) for the lubricating film layer 6) is applied onto the formed hydrophilic film layer 5 and then baked. To form the lubricating coating layer 6. The application method of the resin composition for the lubricating coating layer 6 can be performed by a conventionally known application method such as a bar coater or a roll coater. The coating amount of the resin composition for the lubricating coating layer 6 is appropriately set (adjusted) so that the thickness (adhesion amount) of the lubricating coating layer 6 is 0.01 to 0.8 g / m ² . Further, the baking temperature at the time of forming the lubricating coating layer 6 (the temperature reached by the plate 2) is appropriately set depending on the resin composition for the lubricating coating layer 6 to be applied, but is generally performed in the range of 100 to 200 ° C. .

  When the aluminum fin material 1 (1A) manufactured by the manufacturing method described above is used as an aluminum fin for a heat exchanger, a through-hole through which a heat transfer tube made of a copper tube or the like passes is formed in the plate thickness direction of the fin material. Processed into fins. As a forming method for forming the fin, for example, drawless processing, draw processing, or the like is used.

Draw-less processing can form a collar part having a through-hole through which a heat transfer tube passes with fewer steps than draw processing, and is generally a piercing burring process, a first ironing process, a second ironing process, and a flaring process. A collar portion (not shown) is formed on the aluminum fin material 1 (1A) in the four steps.
The drawing process is the most common molding process that has been performed in the past. The first drawing process, the second drawing process, the third drawing process, the fourth drawing process, the piercing burring process, and the flaring process. Then, a collar portion (not shown) is formed on the aluminum fin material 1 (1A).

  Next, the aluminum fin material of the present invention will be specifically described by comparing an example satisfying the requirements of the present invention with a comparative example not satisfying the requirements of the present invention.

Alloy No. 1200 defined in JIS H 4000: 2006 was used as the plate material (plate thickness 0.1 mm).
A phosphoric acid chromate treatment for forming a base treatment layer was performed on one surface of the aluminum plate. As the chemical conversion treatment liquid, Alsurf (registered trademark) 401/45, phosphoric acid, and chromic acid manufactured by Nippon Paint Co., Ltd. were used. The film thickness of the base treatment layer at this time was 400 mm (Cr conversion value measured by fluorescent X-ray method was 20 mg / m ² ). And after applying and baking the coating material for corrosion-resistant film layers shown in Table 1 with a bar coater to the aluminum plate which gave this phosphoric acid chromate treatment, or the aluminum plate which does not receive phosphoric acid chromate treatment, the hydrophilicity shown in Table 2 The coating for the conductive film layer was applied with a bar coater and baked. Next, the coating material for the lubricating film layer shown in Table 3 was applied onto the surface of the hydrophilic film layer with a bar coater and baked. The thickness of each film depends on the paint concentration and bar coater No. It was adjusted by adjusting. Table 4 shows the thickness (attachment amount) of each coating layer.

  And No. manufactured in this way. For the test materials 1 to 37, the contact angle with water immediately after forming the hydrophilic film layer (described as “initial hydrophilicity” in Table 1) and the surface area ratio were measured. Further, the corrosion resistance, hydrophilic sustainability (described as “hydrophilic persistence” in Table 1), stain resistance, workability, and antibacterial properties of these test materials were evaluated. Measurement or evaluation of these items was performed as follows.

(Initial hydrophilicity)
The base material was formed or not formed on the surface of the test material, and after forming the corrosion-resistant film layer and the hydrophilic film layer, the test material was returned to room temperature. And about 0.5 microliters pure water was dripped at the surface of the hydrophilic membrane | film | coat layer, and the contact angle was measured using the contact angle measuring device (Kyowa Interface Science company make: CA-05 type | mold). A contact angle of 30 degrees or less was accepted (◯), and a contact angle of more than 30 degrees was rejected (x).

(Surface area ratio)
The base material was formed or not formed on the surface of the test material, and after forming the corrosion-resistant film layer and the hydrophilic film layer, the test material was returned to room temperature. Then, the surface of the hydrophilic coating layer in a dry state is measured by three-dimensional measurement using the InnovaAFM (Atomic Force Microscope) manufactured by BRUKER, and the surface area generated by the surface shape of the object (object) The surface area was determined by the following formula (1).
[Formula (1)]
Surface area ratio (%) = {(surface area of target object−designated area surface area) / designated area surface area} × 100

(Corrosion resistance)
Corrosion resistance is in accordance with JIS Z 2371: 2000, a salt spray test for 480 hours is performed, the degree of corrosion of the surface is confirmed, and the degree of corrosion is determined with a specified rating number (hereinafter referred to as “RN”). Evaluation was conducted. R. N. 9.8 or more is particularly good (◎). N. A value of 9.5 or more and less than 9.8 is good (◯). N. 9.3 or more and less than 9.5 is generally good (Δ). N. Less than 9.3 was judged as bad (x).

(Hydrophilic durability)
The hydrophilic durability was evaluated by conducting a hydrophilic cycle test described below. First, after immersing the test material in flowing water having a flow rate of 0.1 L / min for 8 hours, the process of drying the test material at 80 ° C. for 16 hours was performed as 5 cycles for 5 cycles. After carrying out this hydrophilic cycle test, the test material was returned to room temperature, about 0.5 μL of pure water was dropped on the surface, and a contact angle measuring device (Kyowa Interface Science Co., Ltd .: CA-05 type) was used. The contact angle was measured. The running water was performed as described above using tap water and pure water (ion exchange water).
A contact angle of less than 20 ° is particularly good (、), a contact angle of 20 ° to less than 40 ° is good (◯), a contact angle of 40 ° to less than 60 ° is generally good (Δ), and a contact angle of 60 ° or more is bad. (X).

(Contamination resistance (5 types))
After dipping the test material in tap water with a flow rate of 1 L / min for 16 hours, 0.5 g of paraffin, palmitic acid, stearic acid, dioctyl phthalate (DOP), and stearyl alcohol are placed in a glass desiccator with a capacity of 5 L, together with these. The process of encapsulating each test material and heating at 100 ° C. for 8 hours was performed as 5 cycles for 5 cycles. Then, the test material was returned to room temperature, about 0.5 μL of pure water was dropped on the surface, and the contact angle was measured using a contact angle measuring device (Kyowa Interface Science Co., Ltd .: CA-05 type).
A contact angle of less than 40 ° was judged good (◯), a contact angle of 40 ° or more, less than 60 ° was generally good (Δ), and 60 ° or more was judged bad (x).

(Processability)
The workability was evaluated by visually confirming the moldability of the collar portion of the fin after the test material was subjected to drawless processing and draw processing to produce fins, and continuous 10,000 shots were performed.
The case where molding defects such as seizure were not confirmed on the inner surface of the collar portion of the fin after molding was determined to be acceptable (◯), and the case where molding defects were confirmed was determined to be unacceptable (x). In addition, the case where it passed ((circle)) at least one of the drawless process and the draw process was set as the pass in workability.

(Antibacterial)
The antibacterial property was determined by conducting an antibacterial evaluation test against Escherichia coli and Staphylococcus aureus by the film adhesion method specified in JIS Z 2801: 2012 using the prepared test material, and measuring the number of control bacteria. The antibacterial activity value was calculated. The antibacterial activity value is calculated by the following formula. That is, if the number of viable bacteria is 1/100 relative to the number of bacteria in the control group, it is 2 if it is 1/1000.
The antibacterial activity value for each bacterial species was determined according to the following criteria. The case where the antibacterial activity value with respect to either one of the bacterial species was 2 or more was regarded as acceptable.
○: Antibacterial activity value is 2 or more Δ: Antibacterial activity value is 1 or more ×: Antibacterial activity value is less than 1

Table 4 shows the types of base treatment layers, types of anticorrosive coatings, antibacterial agents, hydrophilic coatings and lubricating coatings, initial hydrophilicity evaluation results, and surface area ratio measurement results. The thickness of each coating layer (adhesion amount (g / m ² )), the total adhesion amount of each coating layer (g / m ² ), the corrosion resistance evaluation results, and the hydrophilic sustainability (tap water and pure water) ) Evaluation results, contamination resistance evaluation results, processability evaluation results, and antibacterial evaluation results.

  As shown in Table 4, no. Since the test materials according to Nos. 1 to 6 satisfied the requirements of the present invention, the hydrophilic sustainability was acceptable, and the corrosion resistance, contamination resistance, and workability were also acceptable (all examples). In addition, since the lubricating film layer was not provided, the drawless workability was poor. However, no. Since the test material according to No. 5 contained the inner wax, the workability was extremely good.

No. Since the test materials according to 7 to 24 also satisfy the requirements of the present invention, the hydrophilic sustainability passed, and the corrosion resistance, stain resistance, and workability also passed (Example). In particular, since the lubricating coating layer was provided on the hydrophilic coating layer, the drawless processability was also improved.
In addition, No. In the test material according to No. 14, since the amount of the lubricating film layer was small, molding defects due to insufficient lubrication were confirmed.
No. Since the test material according to No. 15 had a large amount of the lubricating coating layer, color unevenness occurred, but the other performance was satisfactory, and therefore, it was accepted.

  In contrast, no. Since the test materials according to 25 to 37 did not satisfy any of the requirements of the present invention, they resulted in failure in at least one of the evaluation items of corrosion resistance, hydrophilic durability, and contamination resistance (both Comparative example).

No. Since the test material according to No. 25 did not include the base treatment layer, the corrosion resistance was unacceptable.
No. In the test material according to No. 26, since the resin of the corrosion-resistant coating layer was a polyethylene resin, the hydrophilic durability and the stain resistance were unacceptable.
No. In the test material according to No. 27, since the resin of the corrosion-resistant film layer was a vinyl chloride resin, the hydrophilic durability and the stain resistance were unacceptable.
No. In the test material according to No. 28, since the resin of the corrosion-resistant film layer was an ethylene-vinyl acetate resin, the hydrophilic sustainability and the stain resistance were unacceptable.
No. The test material according to No. 29 failed in hydrophilic durability and stain resistance because the resin of the corrosion-resistant film layer was an epoxy resin.
No. In the test material according to No. 30, since the hydrophilic coating layer resin was an acrylic resin, the hydrophilic durability and stain resistance were unacceptable.
No. In the test material according to No. 31, since the resin of the hydrophilic film layer was a polyvinyl alcohol resin, the hydrophilic durability and the stain resistance were unacceptable.
No. In the test material according to No. 32, since the resin of the hydrophilic film layer was polyacrylic acid, the initial hydrophilicity, the hydrophilic durability, and the stain resistance were unacceptable.
No. Since the test material according to No. 33 had an initial hydrophilicity of 30 ° or more, the hydrophilic sustainability and stain resistance were unacceptable.
No. In the test materials according to Nos. 34 and 35, the surface form of the hydrophilic film layer was uneven, and the surface area ratio exceeded 5%, and therefore the stain resistance was unacceptable.
No. Since the test material according to No. 36 did not include a corrosion-resistant film layer, the corrosion resistance, hydrophilic durability, and contamination resistance were unacceptable.
No. In the test material according to 37, since the resin of the hydrophilic film layer was CMC (carboxymethylcellulose sodium), the corrosion resistance, hydrophilic durability, and stain resistance were unacceptable.

DESCRIPTION OF SYMBOLS 1 Aluminum fin material 2 Board | plate material 3 Ground treatment layer 4 Corrosion-resistant film layer 5 Hydrophilic film layer 6 Lubricant film layer

Claims (5)

On the surface of a plate material made of aluminum or an aluminum alloy, a ground treatment layer made of an inorganic oxide or an inorganic-organic composite compound and a corrosion-resistant coating layer (provided that the solid content ratio of the crosslinking agent in the solid content of the corrosion-resistant coating layer is 0.00. An aluminum fin material provided with a hydrophilic film layer in this order, excluding those composed of a resin composition of 2% by mass or more,
The corrosion-resistant coating layer is made of a resin composition containing a corrosion-resistant resin made of a resin having an acrylic resin structure,
The hydrophilic coating layer comprises a monomer having one or more functional groups selected from a sulfonic acid group and an alkali metal base of sulfonic acid, a polymer composed of only the monomer, and the monomer. The contact angle with pure water immediately after forming the hydrophilic film layer and returning to room temperature is 30 degrees or less, comprising a resin composition containing at least one of the containing copolymers, and the surface area ratio The fin material made of aluminum, characterized in that is 5% or less. The corrosion-resistant coating layer contains a corrosion-resistant resin matrix and an antibacterial agent,
The adhesion amount of the corrosion-resistant resin matrix is 0.01 to 8.0 g / m ² ;
The antibacterial agent includes one or more of Zn and Ag, and satisfies at least one of Zn of 0.1 to 40% by mass and Ag of 0.001 to 1.0% by mass with respect to the corrosion-resistant resin matrix. and aluminum fin stock according to claim 1, wherein the total content of the content and the Ag of the Zn containing is less 41 mass%. On the hydrophilic coating layer, further comprising a lubricating coating layer,
The lubricating film layer is made of a resin composition containing at least one lubricating resin selected from the group consisting of polyethylene glycol, modified polyethylene glycol, carboxymethyl cellulose, and alkali metal salts of carboxymethyl cellulose. The aluminum fin material according to claim 1 or 2. A aluminum-made fin stock claimed in claim 3 in which the amount of deposition of the lubricating coat layer is characterized in that it is a 0.01~0.8g / m ^2. The total adhesion amount of each coating layer formed on the surface of the plate material is 0.1 to 10.0 g / m ² per side, 5. The aluminum fin material described in 1.

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