JPH11189882A - Aluminum material for phosphating and its production - Google Patents

Abstract

PROBLEM TO BE SOLVED: To improve phosphating property by burying a particle having a specific particle diameter, which is one of a metallic inorganic compound particle hardly soluble in a specific pH range and a metallic particle hardly soluble in a specific pH range or in a coexisting state of both, in a specific ratio of the coated surface area on the surface of an aluminum material after grinding process and in a preceding step of an alkali defetting process. SOLUTION: The metallic inorganic compound particle is hardly soluble in the alkalinity of 9<pH<=14 and hardly soluble in water of 5<=pH<=9. The metallic particle is hardly soluble in the alkalinity of 9<pH<=14. The particle diameter is 0.0010-5 μm and the ratio of the coated surface area measured in optional 100 μm<2> is 20-80%. The treating method is by sticking a suspension containing 0.01-50 wt.% metallic inorganic compound particle and rubbing or allowing to contact with an aq. solution containing 0.1-50 wt.% inorganic compound of a metallic particle easily soluble in water of 5<=pH<=9 and having 1.0 <=pH<=4.5 and room temp. to 80 deg.C for >=3 sec and rubbing. The coating film adhesiveness after coating is improved.

Description

DETAILED DESCRIPTION OF THE INVENTION

[0001]

BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a phosphating aluminum material used for painting and used as a body of an automobile or a housing of a home electric appliance.
In this specification, aluminum includes both pure aluminum and aluminum alloy.

[0002]

2. Description of the Related Art Conventionally, a steel material is usually used for an automobile body. As this kind of steel material for an automobile body, a surface-treated steel material such as a galvanized steel material or an alloyed galvanized steel material is used in addition to a normal steel material and a high-tensile steel material. Among these, surface-treated steel materials such as galvanized steel materials and alloyed galvanized steel materials have excellent corrosion resistance, and are therefore recommended especially for parts or vehicles that require corrosion resistance.

[0003] In the assembly line of an automobile body using such a steel material, a steel material for the body is formed into a predetermined shape by pressing or the like to form each body part, and then each body part is assembled and spotted. After welding, the assembled body is degreased, and then subjected to a phosphate treatment, a type of chemical conversion treatment, for the purpose of improving the adhesion between the steel material and the coating film and improving the corrosion resistance. It is common to perform painting and normal spray painting. Generally, painted aluminum material is
Corrosion resistance is remarkably excellent if there are no defects such as scratches and pinholes in the coating film.However, if the coating film is damaged by flying stones while driving a car, corrosion of the base aluminum from the damaged part As the coating progresses, the coating bulges, resulting in poor appearance. The poor appearance due to the coating swelling is affected not only by the corrosion resistance of the base aluminum material itself, but also by the uniformity and denseness of the phosphating film as the base material of the coating.

On the other hand, recently, aluminum materials have been increasingly used for automobile bodies mainly for the purpose of weight reduction of the vehicle body for improving fuel efficiency of the automobile. In this case, the entire body of the automobile is rarely aluminized, and generally, a steel material and an aluminum material are used in combination. In order to assemble and manufacture an automobile body using such a steel material and an aluminum material together, it is required to use the same line as in the case of using only the above-described steel material. In other words, after assembling a body part made of molded steel and a body part made of molded aluminum, a body is created, and surface defects such as scratches generated during molding are repaired by grinding, and then the entire body is assembled. Is subjected to a degreasing treatment, followed by a phosphate treatment, followed by electrodeposition coating or spray coating. In this way, even when steel and aluminum are used together, it is not necessary to newly establish another assembly production line,
Moreover, the continuity of the process is maintained, which is advantageous in terms of manufacturing cost. However, in this case, since the aluminum material is subjected to the phosphate treatment simultaneously with the steel material, the following problem occurs.

[0005] That is, when a phosphate treatment is applied to an aluminum material, a phosphate film is not uniformly and densely formed on the aluminum material, and as a result, there is a problem that the corrosion resistance after coating is deteriorated. Furthermore, the aluminum material surface is dissolved during the phosphating treatment, and Al ions are eluted into the treatment bath. Therefore, as described above, the steel material and the aluminum material integrated as an automobile body are simultaneously phosphated. In this case, a passive film of aluminum is formed on the surface of the steel material by Al ions eluted from the aluminum material,
The formation of a phosphate treatment film on the surface of the steel material is also inhibited, and as a result, there is also a problem that sufficient corrosion resistance and sufficient adhesion of the coating film cannot be obtained even for the steel material portion.

[0006]

In a car body maker, the surface is usually adjusted using a colloid solution of a titanium compound (hereinafter referred to as titanium colloid) as a part of the phosphating step. The surface is adjusted by spraying and dipping, but under the conditions of the surface adjusting treatment of the steel sheet, the titanium colloid serving as a nucleus for forming a phosphate film does not sufficiently adhere to the surface of the aluminum material. As one solution to such a problem, the present inventors have disclosed in Japanese Patent Application No.
89199, formed in Japanese Patent Application No. 09/091740.
Prior to forming in the subsequent step of assembling-alkaline degreasing-phosphate treatment, the aluminum material surface is subjected to a treatment (a suspension or an aqueous solution is attached and rubbed) in which fine particles of a metal inorganic compound or fine particles of a metal precipitate are present on the surface of the aluminum material. Improving the phosphatability of the aluminum material side by promoting the adhesion of titanium colloid for surface adjustment or the fine particles themselves acting as nuclei for the formation of a phosphate film, resulting in rapid phosphating film formation and elution of aluminum. Has also applied for something to prevent. However, according to this technique, it has been found that, when grinding is performed after the forming process, fine particles of inorganic compound substances or metal precipitates are removed, and the phosphatability of that portion is reduced.

Also, the present inventors have disclosed in Japanese Patent Application No.
-319919, Japanese Patent Application No. 09-113664, in which fine particles of a metal inorganic compound or fine particles of a metal precipitate are present on the surface of an aluminum material during alkali degreasing and phosphate treatment (a suspension or an aqueous solution is attached and rubbed). Then, the adhesion of titanium colloid for surface adjustment or the fine particles themselves act as nuclei for the formation of a phosphate film, thereby improving the phosphatability of the aluminum material side, and as a result of the rapid formation of the phosphatized film, An application for preventing the elution of aluminum has been filed. Since the grinding is performed between the assembly and the alkaline degreasing, this technique does not reduce the phosphatability of the ground portion after grinding. However, in this technique, it is necessary to add equipment for performing this treatment (adhering and rubbing a suspension or an aqueous solution) between the conventional alkaline degreasing tank and the phosphating tank, and such a space is provided. Existing equipment that cannot be used, the cost of equipment investment increases, and the entire complex body shape after molding must be rubbed separately from the aluminum powder wiping after grinding. There is a problem such as this.

On the other hand, Japanese Patent Application Laid-Open No. 08-099256 proposes a method for preventing the formation of a zinc phosphate film in a grinding portion from decreasing with an Al-Mg alloy containing Cu. That is, it is a method of grinding in the presence of one or more of metals noble than aluminum and oxides of those metals. By doing so, it is difficult to generate an electrochemical difference between the non-ground portion and the non-ground portion of the material in which the Cu is concentrated on the surface by the pickling treatment, thereby preventing the non-uniform amount of the zinc phosphate film from being generated. Specifically, alumina abrasive paper coated with powder of copper, copper oxide, or zinc oxide is used. However, this technique is intended to prevent non-uniformity in the amount of phosphate film formed between the non-grinding portion and the ground portion, but does not increase the amount of phosphate film generation or the coverage of the entire material. Even in this method, even if the metal and the metal oxide adhere to each other, they are ground at the same time so that the metal and the metal oxide do not always adhere uniformly to the ground portion, so that the anode and the cathode are not removed. It does not work well and does not produce a conversion coating sufficient to improve surface properties after painting. Further, this technology is intended for an Al-Mg alloy containing Cu, and from the principle thereof, a material containing no Cu or an Al-Mg alloy.
It seems that it cannot be applied to aluminum alloys other than g alloy.

The present invention has been made in view of the above circumstances, and is intended to repair a surface defect generated at the time of molding, not a target of an alloy having a specific composition, without major equipment remodeling and without much trouble. It is an object of the present invention to provide a method for forming a good phosphate film on the surface of an aluminum material even after grinding.

[0010]

The inventors of the present invention have argued that the reason why the phosphatability of an aluminum material is inferior to that of a steel material is that a phosphate film used for "surface conditioning" after alkali degreasing in ordinary phosphating. It is thought that the titanium colloid, which is said to function as a nucleus for the formation, does not easily adhere to aluminum materials compared to steel materials. In order to improve the phosphatability of the aluminum material, a substance which promotes the adhesion of titanium colloid in the pre-forming stage or a method of directly forming a phosphate film as disclosed in Japanese Patent Application Nos. 08-289199 and 09-091740. Forcibly adhere the core material, and then mold-assemble-
By forcibly adhering a substance that promotes adhesion of titanium colloid or a substance that directly forms a nucleus of phosphate film to at least the ground portion after grinding in the grinding process,
Alternatively, after the assembly-grinding process and before the alkali degreasing step, the titanium surface is applied to all the aluminum surfaces in the ground portion and the non-ground portion without attaching a fine inorganic compound to the aluminum surface in the pre-forming stage. The present inventors have found that the formation of a phosphate film is improved by forcibly adhering a substance which promotes the adhesion of a colloid or a substance which directly serves as a nucleus for forming a phosphate film, and has reached the present invention.

More specifically, the invention according to claim 1 is an aluminum material which is processed in a process subsequent to a forming-assembly-grinding-alkali degreasing-phosphate treatment, and is provided after the grinding process and before the alkali degreasing process. The aluminum surface of the stage is as follows
An aluminum material for phosphate treatment, characterized in that either [A] or [B] or a mixture of [A] and [B] is present. [A] Partially embedded particles of a metal inorganic compound having a particle size of 0.0010 to 5 μm, which is poorly soluble in alkalinity of 9 <pH ≦ 14 and poorly soluble in water of 5 ≦ pH ≦ 9. in state, coating area ratio 2, measured at any 100 [mu] m ²
0 to 80% adhered. [B] A particle having a particle size of 0.0010 to 5 μm which is hardly soluble in alkali having a pH of 9 <pH ≦ 14 is measured at an arbitrary 100 μm ² in a partially embedded state, and the coating area ratio is 20 to
80% adhered.

The invention according to claim 2 is characterized in that the following [C] is added to the surface of the aluminum material at least between the grinding step and the alkali degreasing step, which is the subsequent step of forming, assembling, grinding, alkali degreasing and phosphate treatment. , [D], a method for producing an aluminum material for phosphate treatment. [C] A suspension containing 0.01 to 50 wt.% Of an inorganic compound of a metal which is poorly soluble in alkalinity of 9 <pH ≦ 14 and poorly soluble in water of 5 ≦ pH ≦ 9 is adhered. After that, rub them. [D] 9 <pH ≦ 14
An inorganic compound that is easily soluble in water having a pH of 5 ≦ pH ≦ 9
Room temperature to 80 at 1.0 ≦ pH ≦ 4.5 containing 50 wt.%
After contact with an aqueous solution of 3 ° C. for 3 seconds or more, rubbing is performed. As described above, any one of the processes [C] and [D] may be performed at least between the grinding step and the alkaline degreasing step. Must be given.

Therefore, when perfection is required or when rubbing at this stage is only required to be partially performed, any of [C] and [D] can be performed before the forming step. If such a process is performed, the process between the grinding process and the alkali degreasing process may be performed only on the ground portion, so that this problem is solved. Further, in this case, if the process of [C] is performed twice, the state of claim 1 is the state of claim 1 if the processing of [D] is performed twice, and either of the states of claim [B] is [C]. Either one
In the case of the process [D], a mixed state of [A] and [B] in claim 1 is obtained. The mixed state of [A] and [B] is defined as a particle size of an inorganic compound of a metal which is poorly soluble in alkalinity at 9 <pH ≦ 14 and poorly soluble in water at 5 ≦ pH ≦ 9. ~ 5 μm
And the total coating area ratio of particles having a particle diameter of 0.0010 to 5 μm, which is poorly soluble in alkali having a pH of 9 <pH ≦ 14, is 20 to 80% as measured at an arbitrary 100 μm ^2. Say.

In the fourth and fifth aspects, the inorganic compound of the metal [A] and the inorganic compound of the metal used in the treatment of [C] are titanium oxide, nickel oxide, magnesium oxide, tungsten oxide, niobium oxide, aluminum oxide, Zinc oxide, cuprous oxide, cupric oxide, ferric oxide, molybdenum oxide, magnesium hydroxide, nickel hydroxide, magnesium carbonate, calcium carbonate, zinc phosphate, magnesium oxalate, barium titanate, calcium silicate, hydrogen phosphate One or more selected from magnesium is specified.

Further, in claim 6, the metal particles of [B] are:
It is specified that the inorganic compound is at least one selected from iron, copper, magnesium, manganese, zinc, nickel and tungsten. According to claim 7, the inorganic compound of the metal used in the treatment of [D] is sulfated sulfuric acid. Ferrous iron, copper sulfate, magnesium sulfate,
Manganese sulfate, zinc sulfate, nickel sulfate, ferrous nitrate,
Ferric nitrate, copper nitrate, magnesium nitrate, zinc nitrate, nickel nitrate, ferrous chloride, ferric chloride, copper chloride, magnesium chloride, manganese chloride, nickel chloride, zinc acetate,
One or more selected from nickel acetate, manganese phosphate, and sodium phosphotungstate are specified.

[0016]

DESCRIPTION OF THE PREFERRED EMBODIMENTS An aluminum material for this purpose usually undergoes a process of forming, assembling, grinding, alkaline degreasing and phosphate treatment after being delivered from an aluminum material manufacturer to an automobile body manufacturer. As described above, an automobile body maker usually adjusts the surface with a titanium colloid as a part of the phosphating process. The surface is adjusted by spraying and dipping, but under the conditions of the surface adjustment of the steel sheet, the titanium colloid, which is the nucleus of phosphate film formation, does not sufficiently adhere to the surface of the aluminum material. At the same time, a phosphate film is only sparsely formed.

According to the second aspect of the present invention, it is essential that particles of a substance that promotes the adhesion of titanium colloid or a substance that directly forms a nucleus for forming a phosphate film be forcibly adhered to the surface of the aluminum material at the stage before molding. If this is not performed, the adhesion of the suspension containing the inorganic compound of the metal between the grinding step and the alkaline degreasing step, and the subsequent rubbing, must be performed on the entire surface. . However, this rubbing operation can also serve as a wiping operation of aluminum powder generated during grinding.

On the other hand, in the invention of claim 3, Japanese Patent Application No.
As in the method of 89199 and Japanese Patent Application No. 09-091740, even before molding, particles of a substance that promotes the adhesion of titanium colloid or a substance that directly forms a nucleus for forming a phosphate film are forcibly adhered to the aluminum material surface. in this case,
Since the above-mentioned substance is attached in advance to the grinding section, the attachment of the suspension containing the inorganic compound of the metal between the grinding step and the alkali degreasing step, and the subsequent rubbing, at a minimum, are modified, What is necessary is just to perform only to a grinding part. In addition, since the processing before molding can be performed in a coil state in the case of a plate material, work efficiency is high.

Further, [A] is used in the process [C] of the present invention.
The inorganic compound of the metal forming the state of the above is 9 <pH ≦ 14
Must be hardly soluble in alkali. 9 <pH ≦ 14
When dissolved in alkali, it dissolves in the subsequent alkali degreasing step, so it promotes the adhesion of titanium colloid, which is considered to be the nucleus of phosphate film formation, and also directly acts as the nucleus of phosphate film formation. I will not help.

Further, [A] is used in the process [C] of the present invention.
5 ≦ pH as the inorganic compound of the metal forming the state of
A substance which is hardly soluble in water of ≦ 9 and becomes a suspension is used.
That is, the treatment of [C] has the function of promoting the adhesion of titanium colloid, which is considered to be the nucleus of forming a phosphate film, or the function of directly forming the nucleus of forming a phosphate film, while keeping the metal inorganic compound. This is because it is a process for making it work. When the metal inorganic compound is dissolved and ionized in water of 5 ≦ pH ≦ 9, it is used for the treatment of [C] of the present invention described later, and forms the state of [B].

Examples of the inorganic compound of a metal exhibiting such characteristics include titanium oxide, nickel oxide, magnesium oxide, tungsten oxide, niobium oxide, aluminum oxide, zinc oxide, cuprous oxide, cupric oxide, and secondary oxide. iron,
Molybdenum oxide, magnesium hydroxide, nickel hydroxide, magnesium carbonate, calcium carbonate, zinc phosphate, magnesium oxalate, barium titanate, calcium silicate,
Magnesium hydrogen phosphate and the like may be mentioned, and one kind selected from these may be used, or two or more kinds may be mixed and used.

The particle size distribution of the inorganic compound of the metal suspended in the solution may extend over a wide range.
Since it is considered that particles having a size of from 10 to 5 μm exert the above-mentioned action, the particle size range of the inorganic compound of the metal adhered to the surface of the aluminum material is set to this range. Particle size 0.0010
If it is less than μm, through the promotion of adhesion of titanium colloid,
Or, it does not directly act as a nucleus for forming a phosphate film. If particles having a particle size of more than 5 μm adhere to the surface of the aluminum material, they do not directly function as nuclei for forming a phosphate film. However, when the surface is adjusted, titanium colloid adheres around large particles and phosphoric acid Since the phosphate film forms nuclei for forming the salt film, the phosphate film becomes granular, thereby deteriorating the adhesion of the phosphate film itself and deteriorating the adhesion of the coating film and the appearance (coating property) after coating. For the same reason as above, the particle size of the metal inorganic compound is preferably 0.0050 to 3 μm,
0100 to 1 μm is more preferable. The coverage of the particles of the metal inorganic compound is ²⁰ to 8 as measured at an arbitrary 100 μm ^2.
0%. If it is less than 20%, the particle coverage is low and the effect of accelerating the adhesion of titanium colloid or the effect as a direct nucleus for forming a phosphate film is small. Therefore, the number of nucleus sites for forming the phosphate film is too small, and the crystal size of the phosphate film is reduced. Also, it does not exhibit sufficient effects such as improvement of the film coverage. On the other hand, if the coverage of the particles of the metal inorganic compound exceeds 80%, the particles are continuously formed into large agglomerates, and the phosphate film is formed through the action of promoting the adhesion of the titanium colloid or directly. Since the number of nucleation sites becomes too small and the phosphate film is sparsely formed, not only the phosphate film coverage is reduced and the phosphate film crystal size is increased, but also aluminum in the phosphate bath is reduced. Does not act to suppress the dissolution of

The method of making the coating rate 20 to 80% by measuring the particle size of the metal inorganic compound in a state of being partially embedded in the surface of the aluminum material at an arbitrary 100 μm ² is as follows. First, 0.01 to 5 inorganic compounds of these metals are used.
A suspension containing 0 wt.% Is deposited on the metal surface. This is done by spraying the suspension on an aluminum material or immersing the aluminum material in the suspension. By attaching the suspension to the plate surface using the suspension, uniform attachment can be achieved. If the particles of the inorganic compound of the metal are rubbed on the surface of the aluminum material in powder form without using a suspension, the particles cannot be uniformly adhered but also damage the surface of the aluminum material. Particle size 0.00 as described above
It is considered that the particles of the metal inorganic compound of 10 to 5 μm exert the above-mentioned action. However, since the diameter of the particles is reduced by suspending in a liquid or rubbing operation described later, the particle size distribution before suspending in the liquid is as follows. It may cover a wide range. Thereafter, the inorganic compound particles are partially embedded by rubbing in a state where the inorganic compound particles are not completely dried. "Partially embedded" refers to a state where the particles are completely embedded in the aluminum material, not a state where the particles are not slightly embedded in the aluminum material, but a state where some of the particles are embedded in the aluminum material . By rubbing in a completely dry state, the surface of the plate is less likely to be scratched than in rubbing in a completely dry state, and is evenly and uniformly attached. In this specification, “rubbing” refers to an operation of mechanically rubbing to attach particles to the surface of an aluminum material. Specific examples include brushing using a brush roll, and a method under light pressure using a rubber roll, a sponge, a nylon brush, or the like. In the present invention, this rubbing work is
This can also serve as the work of wiping off aluminum powder generated during grinding, and this can prevent an unnecessary increase in labor.

The suspension used contains an inorganic compound of a metal in a concentration of 0.1.
It is contained at a concentration of 01% to 50%. When the concentration of the inorganic compound is less than 0.01%, the particle coverage is low, and the number of nucleation sites for phosphate film formation, which has little effect as a phosphate film formation nucleus through promotion of adhesion of titanium colloid or directly, is small. Is too small to exert sufficient effects such as the effect of suppressing elution of aluminum into the phosphate bath, the miniaturization of the phosphate film crystal size, and the improvement of the film coverage. If the concentration is more than 50%, not only the cost becomes high but also the particle coverage becomes too high and the particles are continuously formed, and the phosphate film is formed through the action of promoting the adhesion of titanium colloid or directly. The number of nucleation sites becomes too small, the crystal size of the phosphate film increases, and the phosphate film is formed only sparsely, which not only reduces the phosphate film coverage but also elutes aluminum into the phosphate bath. Does not act as a control.
Therefore, the concentration is set to 0.01% to 50%, but more preferably 0.1% to 10% for the same reason.

Further, the metal particles forming the state [B] of the present invention need to exhibit poor solubility in an alkali having a pH of 9 <pH ≦ 14. Metals exhibiting such properties include iron,
Examples thereof include copper, magnesium, manganese, zinc, nickel, and tungsten. In the present invention, one of these may be used, or two or more thereof may be used in combination.

The inorganic compound of the metal used in the treatment [D] for forming the state [B] of the present invention is 5 ≦ pH ≦
Use the one that is dissolved in water and ionized. It is [D]
The treatment is to promote the adhesion of titanium colloid, which is considered to be the nucleus of phosphate film formation in the form of precipitated metal particles, or to directly act as the nucleus of phosphate film formation. That's why. If the inorganic compound is not dissolved in water of 5 ≦ pH ≦ 9, it will be used in the treatment of [C] in order to form the state of [A] of the present invention described above.

Examples of the metal inorganic compound having such characteristics include a sulfuric acid compound, a nitric acid compound and a chlorine compound. Specifically, ferrous sulfate, copper sulfate, magnesium sulfate, manganese sulfate, zinc sulfate, nickel sulfate, ferrous nitrate, ferric nitrate, copper nitrate, magnesium nitrate, zinc nitrate,
Nickel nitrate, ferrous chloride, ferric chloride, copper chloride, magnesium chloride, manganese chloride nickel chloride, zinc acetate, nickel acetate, manganese phosphate, sodium phosphotungstate, and the like. One kind may be used, or two or more kinds may be mixed and used.

The particle size distribution of the metal particles used may extend over a wide range.
Since the particles of μm are considered to exert the above-mentioned action, the metal particles are present at least on the surface of the aluminum material as particles having a particle size of 0.0010 to 5 μm in a partially embedded state after precipitation and rubbing. There is a need to. When the particle size is less than 0.0010 μm, it does not function to form a nucleus for forming a phosphate film or to promote adhesion of titanium colloid. When particles having a particle size exceeding 5 μm are present in a state of being partially embedded in the surface of the aluminum material, the metal is not consumed during the phosphating treatment, and the metal exists under the phosphate film, and the adhesion of the phosphate film is increased. And the adhesion after painting and the corrosion resistance after painting are deteriorated.

The coverage of the metal particles is 20 to 80% as measured at an arbitrary 100 μm ² . If it is less than 20%, the nucleus for forming the phosphate film or the function of accelerating the adhesion of the titanium colloid is so small that no sufficient effect is exhibited. On the other hand, if the coverage of the metal particles exceeds 80%, the particles are partially continuous, and the metal is not consumed during the phosphating treatment and remains as a metal under the phosphate film, so that the adhesion after coating, Corrosion resistance is reduced.

The metal particles are deposited on the surface of the aluminum material.
A method of measuring at an arbitrary 100 μm ² in a partially embedded state and making it exist at a coverage of 20 to 80% is as follows. First, an aqueous solution of an inorganic compound of these metals is brought into contact with an aluminum material at room temperature or higher and 80 ° C. or lower for 3 seconds or longer to deposit a metal. To do this, an aqueous solution is sprayed on the aluminum material or the aluminum material is immersed in the aqueous solution. In addition, the cathode electrolytic treatment may be performed by immersion in an aqueous solution of an inorganic compound. By depositing the metal on the aluminum surface and then rubbing it forcibly, the deposited metal can be made finer and the metal particles can be uniformly attached to the plate surface in a partially embedded state. Rubbing of the deposited metal can be performed in the same manner as rubbing of the inorganic compound particles of [C].

After the step of the present invention, a phosphate treatment such as a zinc phosphate treatment may be performed according to a conventional method. The amount of the phosphate coating is preferably 1.0 to 5 g / m ² . Although it is preferable to perform normal surface conditioning as part of the phosphating treatment, the present invention can omit the surface conditioning. When the surface is adjusted, the coverage of the phosphate film is slightly improved as compared with the case where the surface adjustment is not performed. In particular, when the particle size of the metal inorganic compound is large, there is no nucleation action of the phosphate film itself, but when the surface is adjusted, the phosphate film is formed by using titanium colloid attached to the surface of the large particle as a nucleus. Generate. However, since the coating covers large particles, the coating properties and coating adhesion are not improved. Since the surface adjustment is performed as a part of the phosphate treatment, 20 to 80% of the metal inorganic compound particles having a particle diameter of 0.0010 to 5 [mu] m are adhered at a covering area ratio in the previous stage. The aluminum material according to the treatment method of the present invention has a phosphate coating crystal size of 6 μm because the number of nucleation points for the formation of the phosphate coating increases through promoting the adhesion of titanium colloid in the surface conditioner or directly. A uniform coating is formed below, and the coating is excellent in coating adhesion when applied afterwards and put to practical use.

According to the method for phosphating aluminum material of the present invention, the component composition of the aluminum material is not particularly limited as long as it is subjected to phosphating and used for coating purposes. In addition, various aluminum alloys can be used. In particular, in the case of the use of an automobile body, which is the main object of the present invention, Al-Mg based alloy (JIS 5000 series alloy), Al-Mg-Si
Series alloy (JIS No. 6000 series alloy) is most suitable. The method of manufacturing the aluminum base material itself is not particularly limited, and a rolled sheet having a necessary final thickness may be obtained through ordinary manufacturing steps such as casting, heating, hot rolling, cold rolling, and annealing. Further, the present invention can be applied to a cast material, an extruded material, a forged material, and the like.

[0033]

The chemical composition of the aluminum alloy used in the present invention is shown in Table 1.

[0034]

[Table 1]

5 commonly used for automobile bodies
5182 as a representative of 000 series alloy and 6000 series alloy
And 6101 were used. For both alloys, those having a particularly small Cu content within the specified range were used. This is because when the amount of Cu is large, the phosphatability is improved as a whole, and a difference in the phosphatability is difficult to occur.

The preparation of the test material was performed as follows.

Inventive Examples 1 to 20 corresponding to the twice treatment using the suspension of [C] in the method of claim 3, an aluminum plate having a composition of Table 1 having a thickness of 1.0 mm was prepared at room temperature. The particles of the inorganic compound of the metal shown in Table 2 were immersed in a liquid obtained by mixing and suspending the particles in pure water, and the surface was rubbed with a nylon brush. A high pitch paper (manufactured by Sankyo Rika Co., Ltd.) was mounted on a dual action sander (manufactured by Kuken Co., Ltd.) and ground, and the same inorganic compound particles as shown in Table 2 were mixed with pure water. After being immersed in the suspended liquid and rubbing the surface of the aluminum alloy having the above composition with a nylon brush, alkali degreasing (FC-L4460: manufactured by Nippon Parkerizing Co., Ltd., 43 ° C.)
× 2min pH = 10.5) → Washing → Surface adjustment (PL-
4040: manufactured by Nippon Parkerizing Co., Ltd. Room temperature x 30 seconds
c) → Zinc phosphate (PB-L3020: manufactured by Nippon Parkerizing Co., Ltd., 43 ° C. × 120 sec) → washing with water → drying, followed by phosphate treatment.

Inventive Examples 21 to 22 corresponding to a single treatment using the aqueous solution of [C] in the method of claim 2, and immersion of the inorganic compound in the particle suspension and grinding with a nylon brush. Some were performed only after grinding, but not before.

Inventive Examples 23 to 44 corresponding to the treatment twice using the aqueous solution of [D] in the method of Claim 3: The surface of a 1.0 mm thick aluminum plate having the composition shown in Table 1 Immersed in an aqueous solution of a metal inorganic compound at room temperature to 80 ° C. and contacted for a certain period of time, rubbed with a nylon brush, and supposed to be scratched at the time of molding, # 120 ground paper (high pitch paper: Sankyo Rika Co., Ltd.) is mounted on a dual action sander (Kuken Co., Ltd.) and ground.
Room temperature to 80 ° C. of the inorganic compound of the metal shown in Table 3 as above
Immersed in an aqueous solution of an aluminum alloy, and rubbed with a nylon brush on the surface of the aluminum alloy having the above component composition.
C-L4460: 43 ° C x 2 manufactured by Nippon Parkerizing Co., Ltd.
min pH = 10.5) → Washing → Surface adjustment (PL-40)
40: room temperature x 30 sec, manufactured by Nippon Parkerizing Co., Ltd.) →
Zinc phosphate (PB-L3020: manufactured by Nippon Parkerizing Co., Ltd., 43 ° C. × 120 sec) → washing with water → drying was subjected to a phosphate treatment. The pH of the aqueous solution of the inorganic compound is p
When H is high, an acid such as sulfuric acid, nitric acid or hydrochloric acid is added, and when the pH is low, sodium hydroxide is added so that 1.0 ≦ pH ≦
It adjusted so that it might be in the range of 4.5.

Inventive Examples 45 to 46 corresponding to the one-time treatment using the suspension of [D] in the method of claim 2, and immersed in an aqueous solution of an inorganic compound at room temperature to 80 ° C. Some rubbing was performed before grinding, but only after grinding.

Inventive examples 47 to 48 of the method according to claim 3, which correspond to a double treatment using an aqueous solution of [C] before molding and a suspension of [D] after grinding. Among the methods, invention examples 49 to 50 corresponding to the double treatment using the suspension of [D] before shaping and the use of the aqueous solution of [C] after grinding: Inventive examples changed by the combination of [C] and [D] were also prepared. Inventive Example 47 shows the treatment “before molding” in Table 3.
In the same aqueous solution as in Inventive Example 27, the "after grinding" treatment was performed under the conditions of Inventive Example 9 in Table 2, and in Inventive Example 48, the "before molding" treatment was the same as that of Inventive Example 24 in Table 3. The process "after grinding" was performed using an aqueous solution under the conditions of Invention Example 3 in Table 2. Invention Example 49 was obtained by performing the “before molding” treatment with the same suspension as that of Invention Example 9 in Table 2 and performing the “after grinding” treatment under the conditions of Invention Example 27 in Table 3; The process "before molding" was performed with the same suspension as in Invention Example 3 in Table 2, and the process "after grinding" was performed under the conditions of Invention Example 24 in Table 2.

A comparative example corresponding to the treatment twice using the suspension of [C] in the method of claim 2; for comparison, comparative example 1: the particle diameter of the inorganic compound, 3: A comparative example was prepared in which the concentration of the suspension and the particle coverage were outside the ranges of the present application.

A comparative example corresponding to the treatment twice using the aqueous solution of [D] in the method of claim 2: Further, for comparison, Comparative example 4: Metal particle coverage, Comparative examples 5 to 6: Metal A comparative example was prepared in which the particle size and the particle coverage of the particles were out of the range of the present application.

Conventional Example: Further, the following conventional example was prepared for comparison. Conventional example 1: A suspension treatment and a treatment for forcibly attaching metal inorganic compound particles, or an aqueous solution treatment and a treatment for forcibly attaching metal particles are never performed. . Conventional Examples 2-3: Grinding by attaching an inorganic compound of powder of magnesium oxide and tungsten oxide to # 120 ground paper corresponding to the invention of JP-A-08-099256. Those that do not perform the treatment for forcibly attaching the inorganic compound particles of the metal before grinding. Conventional Examples 4 to 6: After performing a suspension treatment and a treatment for attaching an inorganic compound before grinding corresponding to Japanese Patent Application No. 08-289199, grinding with # 120, and after the grinding, suspension treatment and an inorganic compound No treatment to adhere Conventional Examples 7 to 9: After performing an aqueous solution treatment and a treatment for attaching metal particles before grinding corresponding to Japanese Patent Application No. 9-113464, # 120 grinding was performed, and after grinding, a suspension treatment and an inorganic compound were adhered. Those that do not perform the processing to be performed.

EPMA was mainly used to measure the particle diameter and particle coverage of the inorganic compound and metal particles, and SIMS was used for particles smaller than 0.1 μm which could not be measured by this method.

With respect to the test pieces prepared by these methods,
Between the grinding step and the alkaline degreasing step, first, the particle coverage, the phosphate (zinc phosphate) film coverage, and the phosphate (zinc phosphate) film crystal size were measured. In addition, after the phosphate (zinc phosphate) treatment, the test pieces subjected to cationic electrodeposition coating (coating thickness: 20 μm) were examined for coating properties and coating adhesion.

The measuring method and evaluation method of each measurement item are shown below. Zinc phosphate coating coverage The higher the coating coverage, the better the finish of the coating without the occurrence of citron skin on the coating after electrodeposition coating. In the present invention, S
The film coverage was visually evaluated by EM (× 300) observation. If the coverage is 90% or more, the performance of the coating film surface after coating is satisfactory.で あ れ ば If the coverage is 80 to 89%, the performance of the coating film surface after coating is practically sufficient. ○ If the coverage is 60 to 79%, the performance of the coating film surface after coating can be used. Δ If the coverage is 59% or less, the performance of the coated film surface after coating cannot be used. × Zinc Phosphate Film Crystal Size The smaller the film crystal size, the higher the film coverage and the better the paintability and corrosion resistance. The larger the film crystal size, the lower the coverage and the lower the coatability and corrosion resistance.
In the present invention, the average particle size was measured by SEM (× 1500) observation. If it is 6 μm or less, it is satisfactory. A: 7 to 8 μm is practically sufficient. ○ If it is 9 to 12 μm, it can be used. Δ If it is 13 μm or more, it cannot be used. × Coating Film Properties In the present invention, the surface roughness of the electrodeposited coating film (the degree of yuzu skin) and the state of occurrence of granular bumps were visually determined. ◎ There is neither citron skin nor lumps. ○ Weak skin, no lumps. △ No bumps in citron skin. × There are lumps in citron skin. Coating Film Adhesion In the present invention, the number of remaining coating films was measured and evaluated by immersion in cross-cut tape after immersion in pure water at 40 ° C. for 240 hours. 100 (no peeling) is perfect. ９８ 98 to 99 is practically sufficient. ○ If it is 95-97, it can be used. If it is not more than 94, it cannot be used. ×

[0048]

[Table 2]

[0049]

[Table 3]

[0050]

[Table 4]

It should be noted that, in Japanese Patent Application Nos. 08-289199 and 09-091740, it is known that the non-ground portion has good results. The observation result is described at the center. In Table 2, the treatment of depositing the suspension of the metal inorganic compound and then rubbing is referred to as “metal-inorganic compound adhesion treatment”, and is a process subsequent to molding, assembly, grinding, alkali degreasing, and phosphate treatment. When the treatment was carried out before the forming step, ○ was given in the column “Before molding”, and when the treatment was carried out between the grinding step and the alkali degreasing step, ○ was given in the column “After grinding”. In Table 3, the treatment of depositing an aqueous solution of a metal inorganic compound and then rubbing is referred to as “metal deposition treatment”, and is a molding step of a step following molding-assembly-grinding-alkaline degreasing-phosphate treatment. "Before molding" if processed before
In the column of, when the treatment was performed between the grinding step and the alkaline degreasing step, ○ was given in the column of “after grinding”. Table 4
Within, the "suspension of the metal inorganic compound" and the "aqueous solution of the metal inorganic compound" are collectively referred to as "treatment liquid"
When the "metal-inorganic compound adhesion treatment" and the "metal adhesion treatment" are collectively called "particle adhesion treatment", and the treatment is performed before the molding step in the process following the molding, assembly, grinding, alkali degreasing, and phosphate treatment. In the column of “before molding”, a circle was given in the column of “Before molding”, and when the treatment was performed between the grinding step and the alkaline degreasing step, in the column of “After the grinding”. Although not described in detail in the table, the specific conditions of each process are the same as the corresponding processes in Tables 2 and 3. In addition, observation of the presence state of the particles was omitted.

Tables 2, 3 and 4 show the results of these measurements together with the above processing conditions.

In Examples 1 to 22, 23 to 46, and 47 to 50, the zinc phosphate coating coverage, zinc phosphate crystal size, and electrodeposition coating adhesion were all “perfect”. The evaluation was “sufficient for practical use”. From this result, it is clear from the results that the rubbing treatment of the inorganic compound or the metal particles before and after the grinding was carried out even in the ground portion even in the case of Japanese Patent Application No. 08-108,087.
It can be seen that the tendency is the same as that of Japanese Patent Application No. -289199 or Japanese Patent Application No. 09-091740. Inventive Examples 21 and 22 and Inventive Examples 45 and 46, in which the rubbing treatment of the inorganic compound or the metal particles was not performed before the grinding but only after the grinding, the rubbing treatment of the inorganic compound was performed both before and after the grinding. Almost comparable to the one.

In Comparative Example 1 in which the particle diameter of ferric oxide was as large as 20 μm, since the zinc phosphate film adhered to the surface of the large particles, the surface properties of the electrodeposition coating film and the adhesion of the coating film were inferior. In Comparative Example 2 in which the concentration of nickel oxide in the suspension was as high as 60%, the particle coverage was too high and the particles were continuously generated, and through the action of promoting adhesion of the titanium colloid, or Not only does the number of nucleation sites for direct zinc phosphate film formation become too small, the zinc phosphate film crystal size increases, and the zinc phosphate film is formed only sparsely, so that not only does the zinc phosphate film coverage decrease, but also Both the coating properties and coating adhesion are poor. In Comparative Example 3 in which the concentration of zinc phosphate in the suspension was less than 0.01%, the particle coverage was too low, and the zinc phosphate film-forming nucleus was formed directly or through the effect of promoting the adhesion of titanium colloid. The number of generated nucleus sites is too small, and sufficient effects such as miniaturization of zinc phosphate film crystal size and improvement of zinc phosphate film coverage are not exhibited. As a result, both the properties of the coating film and the adhesion of the coating film deteriorate.

In Comparative Example 4 in which the pH of the aqueous solution of copper sulfate was as high as 5.0, the coverage of metal particles was too low, and nucleation sites for the formation of a zinc phosphate film through the effect of promoting adhesion of titanium colloid or directly. If the number is too small, sufficient effects such as miniaturization of the zinc phosphate film crystal size and improvement of the zinc phosphate film coverage are not exhibited. As a result, both the properties of the coating film and the adhesion of the coating film deteriorate. Comparative Example 5 in which the concentration of an aqueous zinc nitrate solution was as high as 60%
In this case, the particle size of the metal particles was too large, the coverage of the metal particles was too high, and the adhesion of the coating film was deteriorated. In Comparative Example 6 in which the concentration of the aqueous ferrous sulfate solution was as low as 0.05% and the pH was as low as 0.8, the particle size of the metal particles was too large, the coverage of the metal particles was too low, and the adhesion of titanium colloid was observed. The number of nucleation sites for forming the phosphate film through the effect of acceleration or directly is too small, and does not exert sufficient effects such as miniaturization of the crystal size of the phosphate film and improvement of the film coverage. As a result, both the properties of the coating film and the adhesion of the coating film deteriorate.

In the conventional example 1 in which the treatment for forcibly adhering the metal inorganic compound particles or the metal particles is not performed at all, the coverage of the zinc phosphate film is low and the crystal size of the zinc phosphate film is large. As a result, the surface properties of the electrodeposition coating film and the adhesion of the electrodeposition coating film are poor. Magnesium oxide was added to # 120 ground paper without performing the treatment for forcing the metal inorganic compound particles before grinding, which corresponds to the invention of JP-A-08-099256 of Conventional Examples 2-3, to be performed. In the case where the inorganic compound of tungsten oxide powder is adhered and ground, the particle coverage is low, the zinc phosphate coating coverage is low, the zinc phosphate coating crystal size is large, and the electrodeposition coating properties,
Poor coating adhesion. Patent Application No. 08-28 of Conventional Examples 4 to 6
No. 9199, a process of attaching an inorganic compound (magnesium oxide, tungsten oxide, zinc phosphate) before molding, grinding with # 120 grinding paper, and attaching the inorganic compound particles or metal particles after grinding. If not, inorganic compound particles will be removed by grinding.
Zinc phosphate coverage, zinc phosphate film crystal size, coating properties,
The coating film adhesion is close to that of Conventional Example 1. Metallic particles (iron, manganese, zinc) are adhered before molding and are ground with # 120 grinding paper, which corresponds to Japanese Patent Application No. 09-091740 of Conventional Examples 7 to 9, and the inorganic compound particles after grinding Alternatively, in the case where the treatment for adhering the metal particles is not performed, the metal particles are removed by grinding, so that the zinc phosphate coverage, the zinc phosphate film crystal size, the coating properties, and the coating adhesion are close to those of the conventional example 1. turn into.

[0057]

According to the present invention, at least between the grinding step and the alkali degreasing step, which is a step following the forming, assembling, grinding, alkali degreasing, and phosphate treatment, a suspension of a specific metal inorganic compound or After the aqueous solution is applied, rubbing is performed to forcibly adhere the inorganic compound or metal particles of the specific particle size to the aluminum material surface before the alkali degreasing process after the grinding process at a constant coverage area ratio. Since the particles are present in a state where they have been formed, even in the grinding portion, the particles are improved in phosphatability through the action of promoting adhesion of titanium colloid for surface conditioning or directly acting as phosphate film forming nuclei. Let it. In addition, the rubbing work can also be performed by wiping the aluminum powder generated during grinding,
This effect can be exerted on aluminum materials of any composition without any major equipment modifications required when performing similar treatments between alkali degreasing and phosphate treatment. The improvement in phosphatability improves the coatability, thereby obtaining a good coating film and improving the adhesion of the coating film after coating. Therefore, it is also possible to obtain excellent corrosion resistance after painting.

Although not shown in the examples,
As a result of the rapid formation of the phosphate film by acting as a nucleus for the formation of the phosphate film, it also serves to suppress the elution of aluminum into the phosphate bath and prevent the deterioration of the phosphate bath. Therefore, the phosphating method of the present invention is most suitable for applications in which a coating is applied after grinding for repairing surface defects generated during molding of an automobile body or the like, followed by phosphating.

Claims (7)

[Claims] 1. An aluminum material to be processed in a process following a forming-assembling-grinding-alkali degreasing-phosphate treatment,
The surface of the aluminum material after the grinding process and before the alkali degreasing process is any one of the following [A], [B], or [A].
And [B] in a mixed state. [A] Partially embedded particles of a metal inorganic compound having a particle size of 0.0010 to 5 μm, which is poorly soluble in alkalinity of 9 <pH ≦ 14 and poorly soluble in water of 5 ≦ pH ≦ 9. in state, coating area ratio 2, measured at any 100 [mu] m ²
0 to 80% adhered. [B] A particle having a particle size of 0.0010 to 5 μm which is hardly soluble in alkali having a pH of 9 <pH ≦ 14 is measured at an arbitrary 100 μm ² in a partially embedded state, and the coating area ratio is 20 to
80% adhered. 2. The process of forming, assembling, grinding, alkaline degreasing, and phosphate treatment, which is followed by at least between the grinding step and the alkaline degreasing step, includes the following steps on the surface of the aluminum material.
A method for producing an aluminum material for phosphating, which comprises performing any one of the treatments [C] and [D]. [C] A suspension containing 0.01 to 50 wt.% Of an inorganic compound of a metal which is poorly soluble in alkalinity of 9 <pH ≦ 14 and poorly soluble in water of 5 ≦ pH ≦ 9 is adhered. After that, rub them. [D] 9 <pH ≦ 14
An inorganic compound that is easily soluble in water having a pH of 5 ≦ pH ≦ 9
Room temperature to 80 at 1.0 ≦ pH ≦ 4.5 containing 50 wt.%
After contact with an aqueous solution of 3 ° C. for 3 seconds or more, rubbing is performed. 3. The process of forming, assembling, grinding, alkali degreasing, and phosphate treatment, before the forming process, and between the grinding process and the alkali degreasing process, the following [C] And [D], a method for producing an aluminum material for phosphate treatment. [C] A suspension containing 0.01 to 50 wt.% Of an inorganic compound of a metal which is poorly soluble in alkalinity of 9 <pH ≦ 14 and poorly soluble in water of 5 ≦ pH ≦ 9 is adhered. After that, rub them. [D] 9 <pH ≦ 14
An inorganic compound that is easily soluble in water having a pH of 5 ≦ pH ≦ 9
Room temperature to 80 at 1.0 ≦ pH ≦ 4.5 containing 50 wt.%
After contact with an aqueous solution of 3 ° C. for 3 seconds or more, rubbing is performed. 4. The inorganic compound of the metal [A] is titanium oxide, nickel oxide, magnesium oxide, tungsten oxide, niobium oxide, aluminum oxide, zinc oxide, cuprous oxide, cupric oxide, or ferric oxide. , Molybdenum oxide, magnesium hydroxide, nickel hydroxide, magnesium carbonate,
2. The aluminum material for phosphating according to claim 1, which is one or more selected from calcium carbonate, zinc phosphate, magnesium oxalate, barium titanate, calcium silicate and magnesium hydrogen phosphate. 5. The inorganic compound of a metal used in the treatment of [C] is titanium oxide, nickel oxide, magnesium oxide, tungsten oxide, niobium oxide, aluminum oxide, zinc oxide, cuprous oxide, cupric oxide, or oxide. One or more selected from ferric oxide, molybdenum oxide, magnesium hydroxide, nickel hydroxide, magnesium carbonate, calcium carbonate, zinc phosphate, magnesium oxalate, barium titanate, calcium silicate, magnesium hydrogen phosphate The method for producing an aluminum material for phosphating according to claim 2 or 3, wherein: 6. The phosphate treatment according to claim 1, wherein the metal particles [B] are one or more selected from iron, copper, magnesium, manganese, zinc, nickel and tungsten. Aluminum material. 7. The inorganic compound of a metal used in the treatment of [D] is ferrous sulfate, copper sulfate, magnesium sulfate, manganese sulfate, zinc sulfate, nickel sulfate, ferrous nitrate, ferric nitrate, copper nitrate 1, selected from magnesium nitrate, zinc nitrate, nickel nitrate, ferrous chloride, ferric chloride, copper chloride, magnesium chloride, manganese chloride, nickel chloride, zinc acetate, nickel acetate, manganese phosphate, sodium phosphotungstate 4. The method for producing an aluminum material for phosphating according to claim 2, wherein the method is a kind or two or more kinds.