Patent Application
20180340747
The present invention relates to precoated fins, each having a substrate composed of aluminum or an aluminum alloy, and a hydrophilic-coating film, which is formed on a surface thereof, and to a heat exchanger comprising such precoated fins.
Fin-tube heat exchangers are often used, e.g., in air conditioners. Such heat exchangers typically comprise tubing made of copper or aluminum, and numerous plate fins made of aluminum. The tubing passes through the plate fins. The plate fins are formed by casting aluminum or an aluminum alloy, and then hot rolling and cold rolling into a coil shape; a hydrophilic paint or a water-repellent paint is then precoated on both sides.
In recent years, there has been demand for improvement in the heat-exchanging performance of heat exchangers and improvement in the hydrophilicity of the fins with the aim of reducing noise during operation. There is also demand for contamination resistance and water-scattering resistance in the fins of indoor units in order to prevent water scatter and dew scatter and to prolong the hydrophilic performance. In addition, to conserve energy, there is continuing demand for improved defrosting properties in the fins of outdoor units, and the idea of increasing the number of fins by narrowing the fin pitch is being studied.
Air conditioners for home use and for business use comprise indoor units and outdoor units, which are connected by tubing, through which a coolant circulates. In the interiors of the indoor unit and the outdoor unit, there are heat exchangers having fins provided on a coolant-passageway tube; fans for delivering an air draft to the heat exchanger and motors for driving the fans are also respectively disposed in the interiors of the indoor unit and the outdoor unit. A compressor and an expansion valve are incorporated within a passage (conduit) that connects the indoor unit and the outdoor unit, and heat exchange is performed. During a cooling operation, the heat of the coolant, which became high temperature owing to being compressed by the compressor, is dissipated to the outdoor space by the outdoor unit. This cooled-down coolant is then evaporated by being passed through the expansion valve and the evaporated coolant, whose temperature has become low, passes through the indoor unit, so that a cold air draft is supplied to the indoor space. The cooling operation cycle is completed by compressing the coolant, which has absorbed heat from the indoor space, once again by the compressor.
In contrast, during a heating operation, the heat of the coolant, which became high temperature owing to being compressed by the compressor, is discharged to the indoor space by the indoor unit. This cooled-down coolant is then evaporated by being passed through the expansion valve and the evaporated coolant, whose temperature has become low, passes through the outdoor unit and absorbs heat from the outdoor space. The heating operation cycle is completed by compressing the coolant that has absorbed heat from the outdoor space once again by the compressor. Normally, when a heating operation is being performed and the outdoor temperature is low, it is necessary to ensure that the outdoor temperature of the coolant (i.e. the temperature of the coolant while it is in the outdoor unit) is lower than the outdoor temperature so that the coolant can absorb heat from the outdoor space. Consequently, the coolant temperature sometimes becomes 0° C. or lower. However, if the temperature of the coolant becomes 0° C. or lower, then the temperature of the fins that contact the tubing inevitably becomes 0° C. or lower, and therefore moisture in the air adheres to the fins and frost may form on the fins.
If frost adheres to the fins of the outdoor unit, the frost becomes a barrier (a quasi-insulator) between the coolant and the outdoor air, thereby impeding movement (transfer) of heat. In addition, the frost occupies space between the fins, thereby decreasing the amount of air that can flow between the fins decreases, whereby a much greater decrease in heat-exchanging performance results. If an excessively large amount of frost adheres and the heat-exchanging performance decreases, then it becomes necessary to temporarily stop the heating operation and perform a defrosting operation to remove that frost. In the defrosting operation, the coolant that passes through the outdoor unit is heated up to a temperature that will melt the frost on the fins, such that the frost is changed to water by the circulation of the coolant for a fixed time, and the water is subsequently discharged. However, a defrost operation is problematic in that energy is needed to heat the coolant and in that indoor comfort is impaired because the heating operation is temporarily stopped. Consequently, various techniques for reducing the adherence of frost have been proposed.
For example, in the below-identified Patent Document 1, a hydrophilic-coating film containing a hydrophilic resin and cross-linkable fine particles is proposed. Furthermore, as the hydrophilic resin, a hydrophilic-coating film is proposed, in which a metal surface is covered with a hydrophilic film using a hydrophilization treatment agent containing a specified (meth)acrylic resin, polyvinyl alcohol and at least one resin selected from polyethylene oxide and polyethylene glycol.
In the below-identified Patent Document 2, a water-sheeting coating agent is proposed that contains an organosilicon compound component, which is composed of a mixture of a partial hydrolysate of polyorganosiloxane and a partial hydrolysate of fluoroalkylsilane, and an organic solvent capable of dissolving the organosilicon compound component.
In the below-identified Patent Document 3, a water-repellent coating composition composed of an organic-resin solution and fine particles is proposed.
In the below-identified Patent Document 4, a frost-formation-prevention treatment composition is proposed in which a cross-linking agent, a fluorine-based polymer, and an antifoaming agent are admixed into a specified acrylic-modified epoxy resin.
Patent Document 1: Japanese Laid-open Patent Publication 2014-000534
Patent Document 2: Japanese Laid-open Patent Publication 2013-147573
Patent Document 3: Japanese Laid-open Patent Publication H5-117637
Patent Document 4: Japanese Laid-open Patent Publication 2011-102334
With respect to the hydrophilic-coating film of Patent Document 1, because condensed water wets and spreads on the fin surfaces, it is characterized in that the ventilation resistance can be maintained low and heat-exchanging performance is high. However, owing to the effects of that high hydrophilicity, a thin water film tends to be maintained on the fin surfaces. Furthermore, because the hydrophilic-coating film surfaces have a rough unevenness, hydrophilicity is caused to be exhibited, and consequently the water film tends not to flow off. As a result, the hydrophilic-coating film of Patent Document 1 is problematic because frost tends to adhere to the fins of the outdoor unit during a heating operation.
In addition, the water-sheeting coating agent of Patent Document 2 enables a coating film to be formed that excels in water sheeting and can be maintained for a long time. However, the water-sheeting coating agent is suited for postcoating; it is not suited for precoating. In addition, the water-sheeting durability of the coating film formed by the water-sheeting coating agent is insufficient.
Patent Document 3 proposes to lengthen the frost-formation time by making the fin surfaces ultra-water-repellent using a coating having the water-repellent coating composition described above. However, the contact-surface area between the fin surfaces, which have a high coefficient of heat transfer, and the condensed water becomes small. As a result, the surface area over which the fin surfaces contact the air, which has a low coefficient of heat transfer, becomes large, and consequently heat-exchanging performance becomes low. In addition, condensed water tends to turn into ice rather than frost. Consequently, during a defrosting operation (thawing operation), instead of frost melting, the ice tends to drop off, and there is a risk that an ice mass will build up inside the outdoor unit. As a result, a separate apparatus for removing the ice mass that has accumulated inside the outdoor unit becomes necessary.
In Patent Document 4, the frost-formation-prevention treating composition suppresses the formation of frost in the outdoor unit, and thereby a coating that excels in corrosion resistance can be formed. However, water-sheeting is insufficient and therefore there is a demand for further improvement.
In view of one or more of these circumstances, one aspect of the present teachings concerns a precoated aluminum sheet for a fin of a heat exchanger that excels in sheeting of condensed water while also exceling in hydrophilicity over a long time, can sufficiently prevent or inhibit the adherence of frost, and excels in frost removal properties. Heat exchangers are also disclosed.
In another aspect of the present teachings, a precoated aluminum plate for a fin of a heat exchanger preferably comprises:
a substrate composed of aluminum; and
a hydrophilic-coating film formed on at least one surface of the substrate; wherein:
a surface roughness RzL of the hydrophilic-coating film in a rolling-parallel direction of the substrate and a surface roughness RzLT of the hydrophilic-coating film in a rolling-perpendicular direction of the substrate satisfy the relationships RzL≤1.5 μm, 0.3 μm≤RZLT≤2.5 μm, and RzL/RzLT≤0.9; and
a contact angle of a water droplet with respect to the hydrophilic-coating film is 25° or less, and a sliding angle of a water droplet in the rolling-parallel direction of the substrate is 20° or less.
In another aspect of the present teachings, a heat exchanger comprises a fin composed of such a precoated aluminum sheet.
The above-described precoated aluminum sheet includes the hydrophilic-coating film in which the surface roughness RzL and the surface roughness RzLT satisfy the above-mentioned relationships. Furthermore, the contact angle of the water droplet with respect to the hydrophilic-coating film and the water droplet sliding angle are the above-mentioned prescribed values (angles) or less. Consequently, the precoated aluminum sheet excels in hydrophilicity and, even if cohered (condensed) water adheres to a surface, the cohered water tends to slide off. Furthermore, when sliding off, it is possible to prevent wetting and spreading of the cohered water on the surface of the hydrophilic-coating film. Furthermore, the precoated aluminum sheet can maintain such excellent hydrophilicity and sliding-off properties of the cohered water for a long time. Consequently, by using the precoated aluminum sheets in the fins of the heat exchanger, the adherence of frost can be sufficiently prevented or inhibited and the frost removal properties are also excellent.
Next, embodiments of a precoated aluminum sheet and a heat exchanger will be explained.
The precoated aluminum sheet has a hydrophilic-coating film formed on a substrate. The hydrophilic-coating film may be formed on one side of the substrate or on both sides. Preferably, the hydrophilic-coating film should be formed on both sides of the substrate. In this case, the fins for the heat exchanger composed of the precoated aluminum sheets can exhibit excellent hydrophilicity on both sides thereof and can exhibit excellent sheeting of condensed water. Consequently, the adherence of frost to the fins of the heat exchanger can be much better prevented and the frost removal properties can be much more improved.
With regard to the precoated aluminum sheet, the surface roughness RzL of the hydrophilic-coating film in the substrate rolling-parallel direction and the surface roughness RzLT of the hydrophilic-coating film in the substrate rolling-perpendicular direction preferably satisfy the relationships RzL≤1.5 μm, 0.3 μm≤RzLT≤2.5 μm, and RzL/RzLT≤0.9. The substrate rolling-parallel direction is the direction parallel to the rolling direction, and the rolling-perpendicular direction is the direction perpendicular to the rolling direction. It is noted that every surface roughness in the present specification indicates the maximum height roughness according to JIS B0601-2001.
If RzL>1.5 μm, then there is a risk that sheeting of condensed water will tend to decrease. In addition, there is a risk that frost will tend to adhere to the fins composed of precoated aluminum sheets and that removal of the adhered frost will become problematic. In addition, if RzLT<0.3 μm, then there is a risk that hydrophilicity will decrease. In addition, there is a risk that frost will tend to adhere to the fins. From the viewpoint of better preventing these, RzLT≥0.8 μm is more preferable, RzLT≥1 μm is yet more preferable, and RzLT≥1.5 μm is particularly preferable. In addition, if RzLT>2.5 μm, then there is a risk that frost will tend to adhere to the fins and removal of the adhered frost will become problematic. From the viewpoint of better preventing these, RzLT≤2.3 μm is more preferable, and RzLT≤1.8 μm is yet more preferable.
In addition, if RzL/RzLT>0.9, then there is a risk that hydrophilicity and/or sheeting of the cohered (condensed) water will tend to decrease. In addition, there is a risk that frost will tend to adhere to the fins and that removal of the adhered frost will become problematic. From the viewpoint of better preventing these, RzL/RzLT≤0.8 is more preferable, and RzL/RzLT≤0.7 is yet more preferable.
The contact angle of the water droplet with respect to the hydrophilic-coating film is preferably 25° or less. If the contact angle is greater than 25°, then there is a risk that hydrophilicity and sheeting of the cohered water will tend to decrease. In addition, there is a risk that frost will tend to adhere to the fins and removal of adhered frost will become problematic. From the viewpoint of better preventing these, the contact angle is more preferably 20° or less and yet more preferably 15° or less.
In addition, the sliding angle of the water droplet, in the rolling-parallel direction of the substrate, with respect to the hydrophilic-coating film is preferably 20° or less. If the sliding angle is greater than 20°, then there is a risk that hydrophilicity and sheeting of the cohered water will tend to decrease. In addition, there is a risk that frost will tend to adhere to the fins and removal of the adhered frost will become problematic. From the viewpoint of better preventing these, the sliding angle is more preferably 15° or less and yet more preferably 10° or less.
The average film thickness of the hydrophilic-coating film is preferably 0.3 μm or more and 1.5 μm or less. In this case, it is possible to much better prevent a decrease in sheeting of cohered water. In addition, the adherence of frost is better prevented and it becomes easier to better remove adhered frost. Furthermore, there is the possibility of increasing the film thickness beyond the above-mentioned range; however, even if the film thickness is increased excessively, virtually no improvement effect is obtained and the weight of the fins composed of the precoated aluminum sheets becomes large, which is not preferable. The average film thickness of the hydrophilic-coating film is more preferably 0.5 μm or more and yet more preferably 0.6 μm or more.
With regard to the hydrophilic-coating film, a hydrophilic polymer (A) is cross linked by a cross-linking agent (B). At least one type of polymer selected from the group consisting of acrylic-modified epoxy resin, acrylic-cellulose resin, cellulose-melamine resin, cellulose-acetate resin, and polyoxyalkylene resin can be used as the hydrophilic polymer (A). At least one selected from the group consisting of isocyanate, blocked polyisocyanate, and carbodiimide can be used as the cross-linking agent (B). By using a combination of these, the surface roughness RzL and the surface roughness RzLT satisfy the above-mentioned desired relationships, and it becomes easy to achieve a hydrophilic film in which the contact angle and the sliding angle are within the above-mentioned desired ranges.
The acrylic-modified epoxy resin is an epoxy resin that has been modified with an acrylic. The acrylic-modified epoxy resin can be obtained by, for example, the following methods (1)-(3). That is, (1) an acrylic-epoxy resin can be obtained by a method in which a polymerizable unsaturated monomer, such as an acrylic monomer, is polymerized with and grafted onto an epoxy resin by a hydrogen abstraction reaction. (2) The acrylic-modified epoxy resin can also be obtained by esterifying a carboxyl-group-containing polymerizable unsaturated monomer, such as a carboxyl-group-containing acrylic monomer, with the epoxy group of an epoxy resin and causing the acrylic monomer to polymerize at the double bond introduced in the epoxy resin. (3) An acrylic-modified epoxy resin can also be obtained by reacting an epoxy resin and a carboxyl-group-containing acrylic resin. The acrylic-modified epoxy resin manufactured by method (3) is preferable. In this case, the adherence of frost can be better prevented and the corrosion resistance of the hydrophilic-coating film is improved.
The hydrophilic polymerizing agent and the cross-linking agent are mixed, and are coated onto at least one surface of the substrate; a cross-linking reaction that creates amide groups can be initiated by heating. As a result, by making a deterioration in hydrophilicity less likely to happen, which deterioration is caused by the resin, which has functional groups that exhibit hydrophilicity, flowing out to the condensed water during use, a hydrophilic-coating film that better excels in durability of hydrophilicity and sheeting of cohered (condensed) water is obtained.
The substrate is composed of sheet-shaped aluminum. In the present specification, the term “aluminum” includes not only pure aluminum but also aluminum alloys. The surface roughness Rz of the substrate in the rolling-perpendicular direction is preferably 0.5 μm or more and 3 μm or less. In this case, it becomes easier for the surface roughness RzL and the surface roughness RzLT of the hydrophilic-coating film to better satisfy the above-mentioned desired relationships. From a similar viewpoint, the surface roughness Rz of the substrate in the rolling-perpendicular direction is preferably 1 μm or more and 2.5 μm or less and is yet more preferably 1.2 μm or more and 2 μm or less.
The precoated aluminum sheets are used in the fins of the heat exchanger. In at least part of each fin, the rolling-parallel direction of the substrate is preferably disposed in the vertical direction. In this case, the above-mentioned excellent features of the precoated aluminum sheet can manifest sufficiently. As a result, in the heat exchanger, the adherence of frost can be more sufficiently prevented and the frost can be more sufficiently removed. With regard to the phrase “the rolling-parallel direction is the vertical direction” mentioned above, it is noted that it is only necessary that the rolling-parallel direction and the vertical direction coincide with each other in external view; however, the rolling-parallel direction and the vertical direction do not necessarily have to coincide, and some tilt is allowed. The tilt angle can be set to any angle as long as the cohered water that is adhered to the fin flows down.
Normally, when the precoated aluminum sheet is being formed into the fins for the heat exchanger, the rolling-parallel direction of the substrate becomes the longitudinal direction of the sheet-shaped fins (hereinbelow, called plate fins), and the longitudinal direction of the plate fins is disposed perpendicularly (that is, vertically) in the heat exchanger. That is, the rolling-parallel direction of the precoated aluminum sheet becomes the perpendicular direction in the heat exchanger. Accordingly, by imparting satisfactory water sheeting properties in the rolling-parallel direction as in the above-mentioned precoated aluminum sheet, cohered water (also called, for example, condensed water droplets) in the heat exchanger is satisfactorily exhausted.
The precoated aluminum sheet can be manufactured as follows. First, a substrate composed of aluminum is manufactured as follows. Specifically, an ingot is manufactured by casting aluminum (i.e., a casting process). Subsequently, a coil (i.e., an aluminum sheet coiled into a roll shape) is manufactured by heating and rolling the ingot (i.e., a hot-rolling process). Next, the post-hot-rolled coil is cold rolled (i.e., a cold-rolling process). Thus, a substrate composed of aluminum can be obtained. Furthermore, the maximum roughness of the cold-rolled coil in the rolling-perpendicular direction is preferably set to 0.5 μm or more and 3.0 μm or less, as described above. To adjust the surface roughness Rz of the substrate in the rolling-perpendicular direction to the above-mentioned desired range, various rolling conditions, such as the maximum roughness of the cold-rolling rollers in the rolling-perpendicular direction, the rolling speed, the lubricating oil, etc., should be adjusted appropriately. To improve cold rollability, annealing (i.e., an annealing process) may be performed in the course of the cold-rolling process.
Contamination, such as rolling oil, can be removed from the surfaces of the post-cold-rolled coil using an alkaline degreaser, and the surfaces can be etched. Thereafter, a chemical-conversion coating can be formed on the coil surfaces using a chemical-conversion-treatment agent. Chromate treatment, zirconia treatment, and the like are examples of the chemical-conversion treatment. By forming the chemical-conversion coating, adhesion between the substrate and the hydrophilic-coating film and between the substrate and a primer layer, which is described below, can be improved. Subsequently, the coil surfaces can be coated, by roll coating, with a hydrophilic paint for forming a hydrophilic-coating film, thereby forming the hydrophilic-coating film. A paint containing, for example, the hydrophilic polymer (A) and the cross-linking agent (B) described above is used as the hydrophilic paint. The hydrophilic paint can further contain a solvent, various additives, etc.
The viscosity of the hydrophilic paint is preferably set to 5-15 s by taking a measurement using a Ford Cup No. 4 as stipulated in JIS K5400. In this case, it becomes easier to form the hydrophilic-coating film in which the surface roughness RzL and the surface roughness RzLT satisfy the above-mentioned desired relationships. After coating with the hydrophilic paint, the hydrophilic polymer (A) can be cross-linked by the cross-linking agent (B) by heating for several seconds at a temperature of approximately 200° C. By cross-linking the hydrophilic polymer (A), a resin having functional groups that exhibit hydrophilicity tends not to flow out to water. Consequently, the durability of hydrophilicity can be further improved.
In addition, before coating with the water-based paint, it is preferable to form a primer layer. In this case, the primer layer is formed between the substrate and the hydrophilic-coating film, and thereby adhesion between the substrate and the hydrophilic-coating film can be further improved. The primer layer can be formed of at least one selected from the group consisting of a urethane-based primer, an acrylic-based primer, and an epoxy-based primer. The thickness of the primer is preferably 0.3 μm or more and 3 μm or less.
Precoated aluminum sheets are used in the manufacture of the heat exchanger as, for example, described below. Specifically, first, precoated aluminum sheets are strip cut from the coil to obtain a plurality of fins. Subsequently, the fins are subject to slit (hole) formation, louver molding, and collar formation using a press. Subsequently, metal tubes disposed at prescribed locations are passed through the holes provided in the fins so as to stack the fins. After stacking, tube-expanding plugs are inserted into the metal tubes to enlarge the outer diameter of the metal tubes, and thereby the metal tube and the fins are caused to closely contact each other. Thus, the heat exchanger can be obtained.
In the present example, multiple precoated aluminum sheets (specifically, sample E1 to sample E21 and sample C1 to sample C9) pertaining to working examples and comparative examples were prepared, and their characteristics were compared and evaluated. As shown in
In the present example, multiple precoated aluminum sheets (i.e., sample E1 to sample E21 and sample C1 to sample C9) having differing surface roughnesses RzL, surface roughnesses RzLT, water droplet contact angles α, water droplet sliding angles β, and the like were manufactured by modifying the substrate surface roughness Rz, the type of chemical-conversion treatment, the presence and type of primer layer, the composition and the viscosity of the hydrophilic paint used in the manufacture of the hydrophilic-coating film, the film thickness of the hydrophilic-coating film, and the like as shown in Table 1 and Table 2. With regard to the hydrophilic paint, the hydrophilic polymer, the type of cross-linking agent, the mixing ratio, and the like were modified as shown in Table 1 and Table 2. The amount of the chemical-conversion coating formed was 20 mg/m2 in every case. In addition, in every precoated aluminum sheet, the hydrophilic-coating film was formed on both sides of the substrate. In addition, the precoated aluminum sheets 1 in sample E19 to sample E21 had a primer layer 4 between the substrate 2 and the hydrophilic-coating film 3, as shown in
(A) Measurement of Surface Roughnesses Rz, RzL, RzLT
The surface roughnesses were measured using a laser microscope LEXT® OLS-3000 manufactured by Olympus® Corporation. Specifically, first, the magnification of the objective lens of the microscope was set to 100 times, the scan pitch of the laser light was set to 0.05 μm, a surface of each sample was scanned, and thereby surface data was obtained. Subsequently, that surface data was analyzed in specified directions (specifically, in the rolling-parallel direction and the rolling-perpendicular direction), and the roughnesses were calculated. The direction was determined based on the rolling marks, which were recognized by magnification. The measurement length was 130 μm; in the rolling-parallel direction, measurements were performed at seven locations in one visual field; in the rolling-perpendicular direction, measurements were performed at seven locations in each of two visual fields (i.e., a total of 14 locations).
(B) Film Thicknesses of the Hydrophilic-Coating Film and the Primer Layer
Film thickness was measured, using an eddy-current-type coating thickness gauge, at ten arbitrary locations on the surface of the hydrophilic-coating film of each precoated aluminum sheet, and an average film thickness was derived from the arithmetic mean of these measurement values. In addition, in the case of a precoated aluminum sheet having the primer layer between the substrate and the hydrophilic-coating film, film thickness was measured, using the same eddy-current-type coating thickness gauge described above, for the coated aluminum sheet in which the primer layer alone was formed and for the precoated aluminum sheet in which the hydrophilic-coating film was further formed on the primer layer. Furthermore, the average film thickness of the primer layer could be obtained from the measurement results of the coated aluminum sheet, and the average film thickness of the hydrophilic-coating film was derived from the difference between the measurement results (the average value) of the precoated aluminum sheet and the measurement results (the average value) of the coated aluminum sheet.
(C) Contact Angle
A water droplet 19 having a volume of 2 μl was dropped onto the hydrophilic-coating film 3 of each of the precoated aluminum sheets 1 (refer to
(D) Sliding Angle
As shown in
Next, each precoated aluminum sheet was evaluated, as follows, for frost-formation preventability, defrosting properties, hydrophilicity durability, sheeting durability, corrosion resistance, and moisture resistance. In the evaluations of frost-formation preventability and defrosting properties, a heat exchanger for evaluation, which comprised fins composed of precoated aluminum sheets, was used.
As shown in
Each of the heat exchangers 5 was prepared as follows. First, assembly holes (not shown), each having a fin-collar part with a height of 1-4 mm for inserting metal tubes 7 therethrough and fixing such, were formed by press working the plate fins 6. Each plate fin 6 was composed of the above-described precoated aluminum sheets 1 having a thickness of 0.1 mm. After stacking the plate fins 6, separately prepared metal tubes 7 were inserted through the assembly holes. A copper tube having a groove formed on its inner surface by rolling or the like was cut to a standard length and hairpin bent, to form the metal tubes 7. Next, by inserting tube-expanding plugs into one end of the metal tubes 7 and widening the outer diameter of the metal tubes 7, the metal tubes 7 were secured to the plate fins 6. After the tube-expanding plugs were removed, U-bent tubes were joined, by braising, to the metal tubes 7, and thereby each of the heat exchangers 5 was obtained.
(E1) Frost-Formation Preventability
Frost-formation preventability was evaluated using the heat exchangers 5 prepared as described above (refer to
(E2) Defrosting Property
An evaluation similar to that of frost-formation preventability was performed; if the remaining ice after defrosting was 20% or less of the total frost amount, then it was evaluated as “□”; if the remaining ice after defrosting was more than 20% and 40% or less of the total frost amount, then it was evaluated as “◯”; if the remaining ice after defrosting was more than 40% and 80% or less of the total frost amount, then it was evaluated as “Δ”; and if the remaining ice after defrosting was more than 80% of the total frost amount, then it was evaluated as “×.”
(F) Hydrophilicity Durability
Hydrophilicity durability was evaluated by measuring the contact angle after a deterioration trial. First, a cycle in which the precoated aluminum sheet was immersed in ion-exchanged water for 2 min and then dried by air blowing for 6 min was performed 300 times (the deterioration (wear) trial). Subsequently, the contact angle of the water droplet after this deterioration (wear) trial was measured by the method described above. If the contact angle after the deterioration trial was 10° or lower, then it was evaluated as “□”; if it was above 10° and 25° or lower, then it was evaluated as “◯”; if it was above 25° and 30° or lower, then it was evaluated as “Δ”; and if it was above 30°, then it was evaluated as “×.”
(G) Sheeting Durability
Sheeting durability was evaluated by measuring the sliding angle after the deterioration (wear) trial. The deterioration trial is similar to that of the hydrophilicity durability described above, and the sliding angle measuring method is as described above. If the sliding angle after the deterioration trial was 10° or lower, then it was evaluated as “□”; if it was above 10° and 20° or lower, then it was evaluated as “◯”; if it was above 20° and 30° or lower, then it was evaluated as “Δ”; and if it was above 30°, it was evaluated as “×.”
(H) Corrosion Resistance
Using each precoated aluminum sheet, the salt spray test stipulated in JIS Z2371 was performed for 500 h, and post-test corrosion resistance was evaluated. After the test, if a brown discoloring did not appear on the surface of the hydrophilic-coating film, then it was evaluated as “◯”; and if a discoloring appeared, then it was evaluated as “×.”
(I) Moisture Resistance
Using each precoated aluminum sheet, the moisture-resistance test stipulated in JIS H4001 was performed for 960 h, and post-test moisture resistance was evaluated. After the test, if a brown discoloring did not appear on the surface of the hydrophilic-coating film, then it was evaluated as “◯”; and if a discoloring appeared, then it was evaluated as “×.”
| Number | Date | Country | Kind |
|---|---|---|---|
| 2015-228230 | Nov 2015 | JP | national |
This application is the US national stage of International Patent Application No. PCT/JP2016/083953 filed on Nov. 16, 2016, which claims priority to Japanese Patent Application 2015-228230 filed on Nov. 20, 2015.
| Filing Document | Filing Date | Country | Kind |
|---|---|---|---|
| PCT/JP2016/083953 | 11/16/2016 | WO | 00 |
