KR20220058691A - Post-treatment method of aluminum alloys in oxalic acid anodizing and Aluminum alloys manufactured by this method - Google Patents

Abstract

The present invention relates to a method for anodizing and post-treating an aluminum alloy in an electrolyte solution using an oxalic acid, and an aluminum alloy surface-treated by the corresponding method. According to the present invention, optimum conditions are derived when treating the surface of the aluminum alloy through an anodizing process and a post-treatment process. Accordingly, a lightweight material having excellent hardness, acid resistance and corrosion resistance can be provided. The method for post-treating the aluminum alloy in oxalic acid anodizing of the present invention comprises: a pretreatment process; an anodizing process; and a heat treatment process.

Description

Post-treatment method of aluminum alloys in oxalic acid anodizing and Aluminum alloys manufactured by this method

The present invention relates to an anodizing treatment and post-treatment method using an oxalic acid electrolyte capable of efficiently improving the withstand voltage, acid resistance and hardness of an aluminum alloy, and an aluminum alloy having an aluminum oxide film with high properties manufactured by this method.

In general, aluminum anodizing is one of the surface treatment methods for forming a film of aluminum oxide (aluminum oxide film) on the surface of aluminum. It takes advantage of the characteristic of being oxidized to form an aluminum oxide film.

And, when anodizing treatment is performed on the aluminum alloy material, an oxide film having a diameter of several nanometers is uniformly grown up to several tens of micrometers, and the oxide film has high hardness to improve abrasion resistance as well as to improve the aesthetics of the surface Corrosion prevention is possible, so it is very good in corrosion resistance.

Anodizing, ie, anodizing, is carried out in various electrolytes such as sulfuric acid, oxalic acid, phosphoric acid, boric acid, citric acid, and chromic acid, and the sulfuric acid method or oxalic acid method is mainly used.

As the electrolyte used in the anodizing, the sulfuric acid method is mainly used because of its low price and low power consumption as well as excellent wear resistance and corrosion resistance. It is 120V, and the sulfuric acid method has economic advantages with a low applied voltage, but exhibits lower hardness and corrosion resistance than the oxalic acid method.

Recently, various techniques for improving the performance and characteristics of the aluminum alloy material while variously changing the composition of the electrolyte have been proposed.

However, the oxide film formed by the anodizing is porous and has adsorption properties, so it is easy to get dirty and sticks to the hand. Because there is a risk of swelling or discoloration, sealing is performed as a post-processing process.

Sealing process refers to a process that seals the micropores of the anodized film and at the same time fills the inside of the micropores to convert physical properties such as corrosion resistance. An organic material sealing treatment in which an organic material such as treatment or oil is applied or deposited is known.

For example, in Korean Patent Laid-Open Publication No. 2006-120949, a sealing solution of pH 5-6 containing 2 to 6 g/L of nickel complex, 1 to 3 g/L of cobalt complex, and 2 to 6 g/L of boric acid is used. A sealing method of aluminum anodizing characterized in that it is carried out at ~ 100 ° C. for 5 to 20 minutes is disclosed.

However, when the nickel salt is used, there is a problem that skin allergies, contact dermatitis and diseases of the respiratory system occur, and moreover, after 2012, nickel and its compounds are water pollutants according to the Water Quality and Aquatic Ecosystem Conservation Act, etc. It is classified as a , and it is regulated to emit less than 5 ppm.

Korean Patent No. 10-1342340 (Announcement Date: 2013.12.16.) Korean Patent No. 10-1751377 (Announcement Date: 2017.06.27.)

Accordingly, the present invention establishes the optimum anodization treatment conditions through analysis of the electrolytic conditions according to the current density and the characteristics of the aluminum oxide film during anodization of an aluminum alloy by the oxalic acid method, and accordingly anodizing and sealing An object of the present invention is to provide an optimal anodizing treatment method of an aluminum alloy through post-processing such as treatment and/or post-heat treatment, and an aluminum alloy product with excellent physical properties manufactured by the method.

The present invention for achieving the above object relates to an anodizing treatment using an oxalic acid electrolyte of an aluminum alloy and a method for post-treatment thereof (hereinafter referred to as an aluminum alloy surface treatment method), and the present invention removes foreign substances from the surface of the aluminum alloy pretreatment process; and an anodizing process of forming an aluminum oxide film on the surface of the aluminum alloy that has undergone the pretreatment process; and a heat treatment process of heat-treating the aluminum alloy that has been subjected to the anodization process.

In addition, the method for treating an aluminum alloy surface according to the present invention may further include, before performing the heat treatment process, a sealing process in which the aluminum alloy that has been subjected to the anodization process is subjected to a boiling water sealing process.

In addition, the method for treating an aluminum alloy according to the present invention may provide an aluminum alloy having excellent withstand voltage, acid resistance and hardness.

By using the surface treatment method of the present invention, that is, anodizing treatment method and post-treatment method, it is possible to provide an aluminum alloy product having an aluminum oxide film layer that is stable and excellent in properties, and the aluminum alloy product has withstand voltage and acid resistance. And it is possible to provide a lightweight material having a very excellent surface hardness with high commerciality.

1a and 1b respectively show the Vickers hardness measurement results according to the current density of Al5052 and Al6061 aluminum alloy.
2a and 2b respectively show break voltage measurement results according to current density of Al5052 and Al6061 aluminum alloys.

Hereinafter, the present invention will be described in more detail.

Aluminum alloy is attracting attention as an alternative material for steel products as a lightweight material, but has a disadvantage in that properties such as hardness and abrasion resistance are lowered compared to steel products. to improve the insufficient physical properties.

The present invention is a surface treatment method (or anodizing treatment and post-treatment method) of the aluminum alloy is a pretreatment process of removing foreign substances on the surface of the aluminum alloy; and an anodizing process of forming an aluminum oxide film on the surface of the aluminum alloy that has undergone the pretreatment process; and a heat treatment step of performing heat treatment.

In addition, the present invention may perform the heat treatment process after performing the sealing treatment process of boiling water sealing treatment of the aluminum alloy that has been subjected to the anodization treatment process before performing the heat treatment process.

In the surface treatment method of the present invention, the pretreatment process is a process for removing various unnecessary foreign substances from the surface of the aluminum alloy, and a degreasing process, an etching process, and/or a neutralization process are sequentially performed.

For a preferred embodiment, in the degreasing process, the aluminum alloy is immersed in an aqueous solution of citric acid at a concentration of 5 to 15% by weight at 20 to 60° C. for 1 to 10 minutes, and then, preferably in an aqueous solution of citric acid at a concentration of 5 to 15% by weight. After immersion for 3 to 5 minutes at 40 ~ 50 ℃, it can be carried out by washing.

In addition, in the etching process, the aluminum alloy subjected to the degreasing process is immersed in an aqueous sodium hydroxide solution having a concentration of 5 to 10% by weight at 20 to 80° C. for 30 seconds to 5 minutes, and then preferably 5 to 10% by weight of hydroxide. After immersion in sodium aqueous solution at 40 ~ 50 ℃ 1 minute 30 seconds ~ 2 minutes 30 seconds, it can be carried out by washing.

In the neutralization process (or desmut process), the aluminum alloy subjected to the etching process is immersed in an aqueous nitric acid solution having a concentration of 10 to 50% by weight at 15 to 30° C. for 30 seconds to 5 minutes, preferably 20 to 30 After immersion in an aqueous nitric acid solution having a concentration of weight % at 15 to 30° C. for 1 to 2 minutes, washing may be performed.

In addition, the aluminum alloy of the pretreatment process may be a 5000 series aluminum alloy or a 6000 series aluminum alloy. As a specific example of the 5000 series aluminum alloy, it may be an Al5052 aluminum alloy or an Al5083 aluminum alloy. Preferably, Al5052 aluminum alloy can be used. In addition, for a specific example of the 6000 series aluminum alloy, it may be an Al6061 aluminum alloy, an Al6063 aluminum alloy, or a 6N01 aluminum alloy. Preferably, Al6061 aluminum alloy can be used.

Next, in the anodizing process, an aqueous solution of oxalic acid having a concentration of 1 to 5 wt%, preferably an aqueous solution of oxalic acid having a concentration of 1.5 to 4.5 wt%, more preferably 2.0 to 4.2 wt% of oxalic acid It can be carried out using an electrolyte containing an aqueous solution. At this time, if the concentration of the aqueous oxalic acid solution is less than 1% by weight, it takes too long to form an aluminum oxide film, which may cause a problem in that the oxide film properties are deteriorated, and when the concentration exceeds 5% by weight, rapidly Since the film properties may be rather deteriorated due to the increase of the applied voltage and the growth of the film, it is preferable to use an aqueous solution of oxalic acid having the above concentration range as the electrolyte solution.

The anodizing process may be performed at a temperature of 10 to 20° C. and a specific current density by immersing the aluminum alloy subjected to the pretreatment process in the electrolyte containing the electrolyte, and then applying a DC voltage.

At this time, if the anodization treatment temperature is less than 10 ℃, the production cost may increase due to the increase of the applied voltage, and there may be problems. It is preferable to carry out under the above temperature.

The anodizing process may be performed for 2,000 seconds to 5,000 seconds at a current density of 1 to 5 A/dm ² by applying a DC voltage.

More specifically, the anodizing process is a constant current method with a current density of 1.0 to 5.0 A/dm ² (eg, 1 A/dm ² , 1.5 A/dm ² , 2 A/dm ² , 2.5 A/ dm ² , 3 A/dm ² , 3.5 A/dm ² , 4 A/dm ² , 4.5 A/dm ² or 5 A/dm ² ) for 100 to 300 seconds, and then 2,000 seconds in the raised current density range to 5,000 seconds, preferably in the range of 1.2 to 4.5 A/dm ² , more preferably in the range of 1.3 to 3.5 A/dm ² , and still more preferably in the range of 1.5 to 3.0 A/dm ² in the range of 2,000 It can be performed in seconds to 4,500 seconds. At this time, if the current density is less than 1.0 A/dm ² , the aluminum oxide film layer does not grow uniformly, and there may be a problem that the film formation time is too long, and if the current density exceeds 5 A/dm ² , rather the film surface Since this non-uniformity and film properties may be deteriorated, it is preferable to perform the anodization process under the current density.

In addition, during the anodizing process, it may be performed while maintaining the current density constant within the above range, or may be performed while changing the current density in 3 to 4 steps within the above range.

As a preferred example of performing anodization while changing the current density, the current density is in the range of 0.5 to 2.0 A/dm ² , preferably in the range of 1.0 to 1.5 A/dm ² for 100 to 600 seconds (preferably 250 to Step 1 performed for 450 seconds); Current density 1.0 ~ 3.0 A / dm ² range, preferably 1.5 ~ 2.0 A / dm ² At 300 ~ 1,000 seconds (preferably 400 ~ 800 seconds) for a second step; And a current density of 2.0 to 5.0 A/dm ² in the range, preferably 2.0 to 3.0 A/dm ² at 1,000 to 3,000 seconds (preferably 1,700 to 2,300 seconds) in three steps; may be performed continuously. At this time, the current density of each stage is higher than the current density of the previous stage.

For another example, a current density of 0.5 to 2.0 A/dm ² in the range, preferably in the range of 1.0 to 1.5 A/dm ² , for 100 to 600 seconds (preferably 250 to 450 seconds); Current density 1.0 ~ 3.0 A / dm ² range, preferably 1.5 ~ 2.0 A / dm ² The second step is performed for 300 ~ 800 seconds (preferably 400 ~ 700 seconds) in the range; Current density 2.0 ~ 4.0 A / dm ² range, preferably 2.0 ~ 2.5 A / dm ² 3 steps performed for 500 ~ 1,000 seconds (preferably 550 ~ 850 seconds) in the range; and a current density of 2.5 to 5.0 A/dm ² in the range, preferably 2.5 to 3.0 A/dm ² in the range of 500 to 3,000 seconds (preferably 1,000 to 2,000 seconds). . At this time, the current density of each stage is higher than the current density of the previous stage.

When the anodizing process is performed under the above conditions, an aluminum oxide film layer having a thickness of 15 to 60 um, preferably 20 to 50 um, more preferably 20 to 40 um, can be formed on the surface of the aluminum alloy.

In the surface treatment method of the present invention, when describing the sealing process for sealing with boiling water, after washing the aluminum alloy that has been subjected to the anodizing process with water, micropores having a porous structure of an oxide film formed on the surface of the aluminum alloy In order to seal the , a sealing process of immersing the aluminum alloy in a bath containing boiling water sealing solution may be performed to perform a sealing process.

As the boiling water sealing solution, 1) a boiling water sealing solution containing only ultrapure water is used, or 2) a boiling water sealing solution containing ultrapure water and an additive is used, or 3) ultrapure water, an additive and a surfactant The boiling water sealing solution containing

The sealing process is 1) When performing with a boiling water sealing solution containing 100% by weight of ultrapure water, the aluminum alloy is immersed in the boiling water sealing solution at a temperature of 85 to 100 ° C. for 30 to 120 minutes. can,

In addition, 2) the sealing process may be performed using a boiling water sealing solution containing an additive and ultrapure water for pH control and stain prevention, and the additive may include at least one selected from acetic acid, formic acid and citric acid. The additive concentration may be 1 to 10 ml/L, preferably 2 to 8 ml/L, and more preferably 2 to 5 ml/L per 1 L of the sealing solution. At this time, if the concentration of the additive is less than 1 ml/L, stains frequently occur on the surface of the aluminum oxide film layer, which may lead to product defects. Therefore, it is recommended to use it within the above concentration range.

In addition, 3) as the boiling water sealing solution, a boiling water sealing solution containing an additive, a surfactant, and ultrapure water may be used. The additive may include at least one selected from acetic acid, formic acid, and citric acid, and the additive concentration is 1 to 10 ml/L, preferably 2 to 8 ml/L, more preferably 2 to 1 L of sealing solution. 5 ml/L. In addition, the surfactant serves to increase acid resistance, and may include a compound represented by the following formula (1).

[Formula 1]

In Formula 1, R ¹ is a C ₈ ~ C ₁₈ straight-chain alkyl group or a C ₁₀ ~ C ₂₀ pulverized alkyl group, preferably R ¹ is a C ₉ ~ C ₁₆ straight-chain alkyl group or C ₁₀ ~ C ₁₆ pulverized alkyl group, more preferably R ¹ is a C ₁₀ ~ C ₁₄ straight-chain alkyl group.

In addition, M ⁺ in Formula 1 is a monovalent cation, preferably Na ⁺ or K ⁺ , and more preferably Na ⁺ .

And, the concentration of the surfactant is 1 ~ 12 g / L, preferably 2 ~ 10 g / L, more preferably 4 ~ 10 g / L per 1 L of the sealing solution, in this case, the concentration of the surfactant is 1 When it is less than g/L, the effect of improving acid resistance may be insignificant, and when the concentration exceeds 10 g/L, it is preferable to use it within the above concentration range because a problem may occur to halve the effect of sealing the boiling water.

When the sealing process uses ultrapure water, a boiling water sealing solution containing an additive and a surfactant, it may be performed for 30 to 200 minutes at 85 to 100° C., preferably for 30 to 120 minutes at 90 to 100° C. At this time, if the sealing temperature is less than 90 ℃, the sealing efficiency is lowered, and a sufficient effect of improving acid resistance may not be seen. In addition, it is preferable to perform the sealing process under the above temperature due to cracks in the aluminum oxide film due to the sealing process at a high temperature.

After performing the sealing process described above, the aluminum alloy product with excellent withstand voltage, acid resistance and surface hardness can be manufactured by taking out the sealed aluminum alloy from the bath and drying it.

Hereinafter, the present invention will be described in more detail through examples. However, the following examples are examples for better understanding of the present invention, and the scope of the present invention should not be construed as being limited to the following examples.

[Example]

Example 1: Anodizing of aluminum alloy

(1) Pretreatment process

Al5052 aluminum alloy specimens (Al5052 specimens) and Al6061 aluminum alloy specimens (Al6061 specimens) were prepared, respectively.

Next, each of the specimens was added to an aqueous solution of citric acid having a concentration of 10 wt% and degreased at about 45° C. for 3 minutes and 30 seconds, followed by washing.

Next, each of the degreased specimens was put into an aqueous sodium hydroxide solution having a concentration of 10% by weight and etched at about 45° C. for 2 minutes, followed by washing.

Next, each of the etched specimens was added to a 35 wt% nitric acid aqueous solution and neutralized (dismut process) for 2 minutes at about 25°C, washed, and pretreated Al5052 specimens and Al6061 specimens were prepared, respectively.

(2) Anodizing process

After putting each of the Al5052 and Al6061 specimens subjected to the pretreatment process in the electrolytic cell containing 3 wt% oxalic acid aqueous solution (electrolyte), DC voltage is applied, and the current density is 1.5 A/dm ² in a constant current method 100 seconds to 300 seconds After raising for a while, the anodization process was performed under 15° C. while fixing and maintaining the current density at 1.5 A/dm ² . The anodization process time (total electrolysis time) was carried out until the aluminum oxide film layer was formed to about 30 μm, the Al5052 specimen was anodized for 3,900 seconds, and the Al6061 specimen was anodized for 4,400 seconds. carried out.

Examples 2 to 4

The Al5052 specimen and the Al6061 specimen were pre-treated and anodized in the same manner as in Example 1, but the anodization process conditions were changed to form an aluminum alloy with an aluminum oxide film layer of about 30 μm as shown in Table 1 below. Anodizing process was performed until

Example 5

An Al5052 specimen and an Al6061 specimen, which were subjected to a pretreatment process in the same manner as in Example 1, were prepared, respectively.

Next, after putting each of the Al5052 specimen and the Al6061 specimen in an electrolytic bath (15° C.) containing 3 wt% oxalic acid aqueous solution (electrolyte), a DC voltage is applied, and a current density of 1.5 A/dm ² is maintained in a constant current method, while maintaining about 300 After performing for about 500 seconds while maintaining the current density of 2.0 A/dm ² by increasing the output voltage, the output voltage is increased again and the current density is changed by performing for about 2,200 seconds while maintaining the current density of 2.5 A/dm ² Anodizing was performed until the aluminum oxide film layer was formed to about 30 μm. At this time, the total anodization treatment time was 2,500 seconds for the Al5052 specimen and 3,000 seconds for the Al6061 specimen.

Example 6

An Al5052 specimen and an Al6061 specimen, which were subjected to a pretreatment process in the same manner as in Example 1, were prepared, respectively.

Next, after putting each of the Al5052 specimen and the Al6061 specimen in an electrolytic bath (15° C.) containing 3 wt% oxalic acid aqueous solution (electrolyte), a DC voltage is applied, and a current density of 1.5 A/dm ² is maintained in a constant current method, while maintaining about 300 After performing for about 500 seconds by increasing the output voltage and maintaining the current density at 2.0 A/dm ² , then increasing the output voltage again and maintaining the current density at 2.5 A/dm ² After performing for about 700 seconds, then again By increasing the output voltage and maintaining the current density at 3.0 A/dm ² , it was carried out for about 1,500 seconds to change the current density and anodized until the aluminum oxide film layer was formed to about 30 μm. At this time, the total anodization treatment time was 2,300 seconds for the Al5052 specimen and 3,000 seconds for the Al6061 specimen.

division Example 1 Example 2 Example 3 Example 4 Example 5 Example 6 current density
(A/
dm ² ) 1.5 2.0 2.5 3.0 1.5~2.5 1.5~3.0 ascension step step 1 step 3 step 4 Specimen type Al
5052 Al
6061 Al
5052 Al
6061 Al
5052 Al
6061 Al
5052 Al
6061 Al
5052 Al
6061 Al
5052 Al
6061 gun
Electrolysis time (sec) 3900 4400 3000 3200 2600 2900 2100 2300 2500 3000 2300 3000

Comparing the total electrolysis time of Examples 1 to 4 in Table 1, the higher the current density value, the higher the output voltage increases, and the total electrolysis time tends to gradually decrease until the aluminum oxide film layer is formed to about 30 μm. was able to confirm This means that the output voltage is continuously increased in order to maintain the current density value, and the higher the current density, the faster the film formation speed and the electrolysis time is reduced.

And, looking at Examples 5 and 6 in which the current density was increased stepwise, it was confirmed that the electrolysis time and the output voltage were similar even though the final current density values were different. And, the output voltage was higher when proceeding stepwise than Examples 1 to 4 maintained at a constant current density, and the current density was 2.5 A/dm ² (Example 3). when applied and 1.5-2.5 A/dm ² (Example 5) and 1.5-3.0 A/dm ² (Example 6) showed similar electrolysis times.

In addition, the Al5052 specimen showed a relatively shorter total electrolysis time than the Al6061 specimen.

Preparation Example 1

An Al5052 specimen subjected to anodization treatment in the same manner as in Example 1 was prepared. Next, the Al5052 specimen subjected to the anodization treatment was put into a heating furnace at 350° C., and then a heat treatment (post-treatment) process was performed for 60 minutes to prepare a surface-treated aluminum alloy (Al5052).

Preparation 2

An Al6061 specimen subjected to anodization treatment in the same manner as in Example 1 was prepared. Next, the Al6061 specimen subjected to the anodization treatment was put into a heating furnace at 350° C., and then a heat treatment (post-treatment) process was performed for 60 minutes to prepare a surface-treated aluminum alloy (Al6061).

Production Examples 3 to 4

A boiling water sealing solution containing 2 ml/L of an additive containing acetic acid and formic acid in a 1:1 volume ratio with respect to 1 L of ultrapure water and ultrapure water was prepared.

Each of the Al5052 specimen and the Al6061 specimen subjected to the anodization treatment in the same manner as in Example 1 was immersed in the boiling water sealing treatment solution bath for 60 minutes at a temperature of 95° C., then taken out, washed and sealed aluminum alloy specimens prepared.

Next, each of the sealed aluminum specimens is placed in a heating furnace at 350° C., and then a heat treatment (post-treatment) process is performed for 60 minutes, anodizing and post-treatment (sealing treatment and heat treatment) are performed to surface-treated aluminum alloy was prepared, and Preparation Example 3 (Al5052) and Preparation Example 4 (Al6061) were carried out, respectively.

Comparative Preparation Examples 1-2

An Al5052 specimen subjected to anodization in the same manner as in Example 1 was prepared as Comparative Preparation Example 1, and an Al6061 specimen subjected to anodization in Example 1 was prepared as Comparative Preparation Example 2.

Comparative Preparation Example 3: Boiling Water Sealing Treatment

After washing the anodized Al5052 specimen in the same manner as in Example 1 with water, immersing it in a bath containing ultrapure water for 60 minutes at a temperature of 95 ° C. Al5052 specimen) was carried out.

Comparative Preparation Example 4: Boiling Water Sealing Treatment

A boiling water sealing solution containing 4 g/L of sodium lauryl sulfate as a surfactant and ultrapure water was prepared.

In the same manner as in Example 1, the anodized Al5052 specimen was immersed in a bath containing the boiling water sealing solution after washing with water for 60 minutes at a temperature of 95° C. Preparation Example 4 (Al5052 specimen) was carried out.

Comparative Preparation Example 5: Boiling Water Sealing Treatment

A boiling water sealing solution containing 2 ml/L of an additive containing acetic acid and formic acid in a 1:1 volume ratio with respect to 1 L of ultrapure water and ultrapure water was prepared.

In the same manner as in Example 1, the anodized Al5052 specimen was immersed in a bath containing the boiling water sealing solution after washing with water for 60 minutes at a temperature of 95° C. Preparation Example 5 (Al5052 specimen) was carried out.

Comparative Preparation Example 6: Boiling Water Sealing Treatment

After washing the Al6061 specimen anodized in the same manner as in Example 1 with water, immersing it in a bath containing ultrapure water at a temperature of 95° C. for 60 minutes, taking it out, washing and sealing an aluminum alloy specimen prepared in Comparative Preparation Example 6 ( Al6061 specimen) was carried out.

Comparative Preparation Example 7: Boiling Water Sealing Treatment

A boiling water sealing solution containing 4 g/L of sodium lauryl sulfate as a surfactant and ultrapure water was prepared.

In the same manner as in Example 1, the anodized Al6061 specimen was immersed in a bath containing the boiling water sealing solution after washing with water for 60 minutes at a temperature of 95° C. Preparation Example 7 (Al6061 specimen) was carried out.

Comparative Preparation Example 8: Boiling Water Sealing Treatment

A boiling water sealing solution containing 2 ml/L of an additive containing acetic acid and formic acid in a 1:1 volume ratio with respect to 1 L of ultrapure water and ultrapure water was prepared.

In the same manner as in Example 1, the anodized Al6061 specimen was immersed in a bath containing the boiling water sealing solution after washing with water for 60 minutes at a temperature of 95° C. Preparation Example 8 (Al6061 specimen) was carried out.

Experimental Example 1: Measurement of physical properties

The film layer thickness, hardness, acid resistance and corrosion resistance of the surface-treated aluminum alloys of Preparation Examples 1 to 4 and Comparative Preparation Examples 1 to 8 were measured, and the results are shown in Tables 2 to 3 below.

Regarding the measurement method, the thickness of the aluminum oxide film layer was measured using an eddy current type film thickness meter, and the hardness was measured under a load of 0.1 kg.f using a Vickers hardness meter.

And, in the case of acid resistance, after attaching an acrylic pipe with an inner diameter of 20 mm to the surface of the specimen, pouring a 5% by weight aqueous solution of HCl into the acrylic pipe, measuring the time for bubble stream generation was measured, and observed up to 8 hours did.

In addition, corrosion resistance was observed up to 400 hours using a salt spray tester.

division Comparative Preparation Example 1 Comparative Manufacturing 3 Comparative Preparation Example 4 Comparative Preparation Example
5 Comparative Preparation Example 2 Comparative Preparation Example 6 Comparative Preparation Example
7 Comparative Preparation Example 8 aluminum Al5052 Al6061 Film thickness (μm) 30±0.7 30±0.3 31±0.4 30±0.3 29±0.6 30±0.4 31±0.5 30±0.9 Hardness (HV) 414±6 430±10 432±8 465±2 350±7 358±12 360±7 386±8 acid resistance
(minute) 5 >180 >420 >420 8 >180 >420 >420 corrosion resistance
(hr) - >400 >400 >400 - >400 >400 >400

division Comparative Preparation Example 1 Preparation Example 1 Preparation 3 Comparative Preparation Example 2 Preparation 2 Preparation 4 aluminum Al5052 Al6061 Film thickness (μm) 30±0.7 31±0.6 30±0.8 30±0.6 30±0.9 31±0.2 Hardness (HV) 435±6 654±9 504±4 361±7 458±8 378±7

Referring to Tables 2 and 3, it was confirmed that the anodization treatment and sealing treatment had relatively superior hardness, acid resistance and corrosion resistance than the surface treatment performed only the anodization treatment.

In addition, after anodizing, the surface-treated specimens (Preparation Example 1, Preparation Example 2) by performing heat treatment have relatively superior hardness characteristics than the specimens subjected to sealing treatment without heat treatment (Comparative Preparation Examples 3 to 8). was able to confirm that it has

Through this, it can be confirmed that the high hardness characteristics are improved through the post-treatment process of heat treatment or sealing treatment and heat treatment according to the present invention.

The above description is only one embodiment of the present invention, and those of ordinary skill in the art to which the present invention pertains will be able to implement it in a modified form without departing from the essential characteristics of the present invention. Accordingly, the scope of the present invention should not be limited to the above-described embodiments, but should be construed to include various embodiments within the scope equivalent to the content described in the claims.

Claims (8)

A pretreatment process to remove foreign substances from the surface of the aluminum alloy; and
anodizing process of forming an aluminum oxide film on the surface of the aluminum alloy that has undergone the pretreatment process; and
Including;
The heat treatment is a post-treatment method of an aluminum alloy in oxalic acid anodizing, characterized in that performed at 100 ~ 400 ℃ 30 ~ 150 minutes.
The aluminum alloy in oxalic acid anodizing according to claim 1, further comprising a sealing process of boiling water sealing the aluminum alloy that has been subjected to the anodizing process between the anodizing process and the post-treatment process. Post-processing method.
The method according to claim 1, wherein the anodizing process is performed for 2,000 seconds to 5,000 seconds at a temperature of 10 to 20° C. and a current density of 1 to 5 A/dm ² by applying a DC voltage. Post-treatment method of aluminum alloy in oxalic acid anodizing.
According to claim 1, wherein the anodizing process is a post-treatment method of an aluminum alloy in oxalic acid anodizing, characterized in that it is performed in an electrolyte solution containing an aqueous solution of oxalic acid at a concentration of 1 to 5% by weight.
The method of claim 1, wherein the aluminum alloy in the pretreatment process comprises a 5000 series aluminum alloy or a 6000 series aluminum alloy.
The method according to claim 1, wherein the pretreatment process sequentially performs a degreasing process, an etching process, and a neutralization process,
The degreasing process is performed by immersing the aluminum alloy in an aqueous citric acid solution having a concentration of 5 to 15% by weight at 20 to 60° C. for 1 to 10 minutes, followed by washing,
The etching process is performed by immersing the aluminum alloy subjected to the degreasing process in an aqueous sodium hydroxide solution having a concentration of 5 to 10% by weight at 20 to 80° C. for 30 seconds to 5 minutes, followed by washing;
The neutralization process is performed by immersing the aluminum alloy subjected to the etching process in an aqueous nitric acid solution having a concentration of 10 to 50% by weight at 15 to 30° C. for 1 to 2 minutes, followed by washing. Post-processing method.
According to claim 2, wherein the boiling water sealing treatment is performed by immersing the aluminum alloy subjected to the anodizing process in a boiling water sealing treatment solution,
The boiling water sealing solution is
ultrapure water;
containing ultrapure water and additives; or
A post-treatment method of an aluminum alloy in oxalic acid anodizing, comprising: ultrapure water, additives and surfactants.
An aluminum alloy surface-treated by the method of any one of claims 1 to 7.

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