KR20230029374A - Development of Extremely Super-oleophobic (Super-hyhobic) Aluminum 5000 Series Alloys - Google Patents

Abstract

The present invention relates to super-oleophobic (super-hydropic) aluminum 5000-series alloy surface development. In accordance with the present invention, in a method of manufacturing a super-oleophobic and super-hydropic film on a 5000-series aluminum alloy surface, as a cross-linked PDMS derivative represented in Chemical formula 1 and an organic solvent are used at a specific mixing ratio, superhydrophobicity and superoleophobicity can be imparted, and manufacturing costs can be low. Also, since a coating film can be adjusted in thickness to several to tens of nms and can be applied to the coating of a microstructure oxide film, the super-oleophobic and super-hydropic film can be useful for an oil mist collection system/facility, a pipe, a hood, a hood component, a nozzle, a pipeline or the like, requiring superhydrophobicity and superoleophobicity, and, moreover, the super-oleophobic and super-hydropic film can be useful as a machine learning database for super-oleophobic aluminum 5000-series surface treatment technology development.

Description

Development of Extremely Super-oleophobic (Super-hyhobic) Aluminum 5000 Series Alloys}

The present invention relates to the development of a super oil repellent (super water repellent) aluminum 5 thousand series alloy surface.

In general, water repellency and oil repellency mean properties that are difficult to get wet with water and oil, respectively. case is generally defined.

Recently, superhydrophobic surfaces with water contact angles greater than 150° have attracted considerable attention due to their importance in both basic research and practical applications. Superhydrophobicity and superoleophobicity refer to physical properties in which the surface of an object is extremely difficult to get wet with water and oil, respectively. For example, the leaves of plants, the wings of insects, or the wings of birds have characteristics that prevent any external contaminants from being removed without special removal or from becoming contaminated in the first place. This is because plant leaves, insect wings, and bird wings have super-water repellent properties.

Wettability is a key surface property of solid materials, and it is primarily governed by both the chemical composition and the geometrical micro/nanostructure. Wettable surfaces have attracted much attention due to their potential applications in various fields such as oil-water separation, anti-reflection, anti-bioadhesion, anti-adhesion, anti-fouling, self-cleaning and fluid turbulence suppression.

On the other hand, there have been some reports on the production of superhydrophobic aluminum, but superhydrophobicity/superoil repellency on metal substrates has not received relatively much attention.

As air pollution due to recent environmental pollution has become serious and the occurrence of yellow dust and fine dust has increased, there are many cases in which a ventilation device is operated to purify indoor air rather than opening a window to ventilate. In addition, living dust, food odors, cigarette odors, various harmful odors generated during work, and harmful substances such as carbon monoxide generated from residential facilities, business facilities, and commercial facilities such as homes, workplaces, industrial sites, restaurants, offices, toilets, and bathrooms, etc. In order to remove air, fine dust, oil vapor, etc., a ventilation device is also operated at all times.

These ventilation devices are generally implemented by complex facilities such as a ventilation system that is systematized and installed in a specific place and automatically operated according to the degree of indoor contamination, or is a window type ventilator that is installed on a wall adjacent to the outside and simply circulates inside and outside air. is implemented by

However, these ventilators have a problem that dust inevitably accumulates inside and outside the ventilator when used for a certain period of time, which is unsanitary and requires a cumbersome task of separating and washing the ventilator to remove dust.

In particular, there is no filtering device to primarily adsorb oil or fine dust in ventilators installed in restaurants or places where oil vapor is generated. Not only can it pose a serious concern to fire, but it can also be exposed to the risk of fire.

Publication No. 10-2014-0101193

An object of the present invention is to provide a method for producing an oil repellent and water repellent film on the surface of a 5000 series aluminum alloy.

Another object of the present invention is to provide a 5000 series aluminum alloy having an oil repellent and water repellent film produced by the above manufacturing method.

Another object of the present invention is to provide an oil vapor recovery device, a pipe, a hood, and a conduit including a 5000 series aluminum alloy having oil and water repellent films formed by a manufacturing method.

In order to achieve the above purpose,

The present invention is a pre-patterning step (step 1) of first anodizing a 5000 series aluminum alloy at 30-50V for 5-15 hours and then etching to remove the first anodized film. ;

Secondary anodic oxidation treatment of the 5000 series aluminum alloy for which pre-patterning has been completed in step 1 at 75-85V for 25-35 seconds (step 2);

pore widening by immersing the 5000 series aluminum alloy subjected to secondary anodization in step 2 in a 0.05-1.0M phosphoric acid (H ₃ PO ₄ ) solution for 55-65 minutes (step 3);

subjecting the 5000 series aluminum alloy to which the pore expansion is completed in step 3 at 75-85V for 25-35 seconds (step 4); and

Coating with a coating composition containing a cross-linked polydimethylsiloxane (PDMS) derivative represented by Formula 1 and an organic solvent (step 5); including,

Provided is a method for producing an oil repellent and water repellent film on the surface of a 5000 series aluminum alloy.

[Formula 1]

(In Formula 1, x and y are each an integer of 1-30.)

In the manufacturing method according to the present invention, steps 1 to 4 form an anodized film of a Pillar-On-Pore (POP) structure on the surface of the 5000 series aluminum alloy through anodization and pore expansion treatment. It is a manufacturing step to form. Here, the anodized film exhibits hydrophilicity, and the anodized film of the POP structure according to the present invention exhibits superhydrophilicity. Here, the coating composition according to step 5 is to impart oil repellency and water repellency, and as the thin coating is applied to the micronano surface of the POP structure to a monomolecular thickness level, the micronano surface structure of the anodized film is maintained, resulting in oil repellency and water repellency. It is a technical feature to maximize the effect.

In the manufacturing method according to the present invention, the second anodizing in step 2 and the third anodizing in step 4 use hard anodizing conditions of anodizing at 75-85V for 25-35 seconds, respectively. anodic oxidation treatment, and the pore expansion in step 3 may be immersing the aluminum alloy subjected to the secondary anodization treatment in step 2 in a 0.05-1.0M phosphoric acid (H ₃ PO ₄ ) solution for 55-65 minutes, , Preferably, the second anodizing in step 2 and the third anodizing in step 4 are anodized using hard anodizing conditions of anodizing at 78-82V for 28-32 seconds, respectively. And, the pore expansion in step 3 may be immersing the aluminum alloy subjected to the secondary anodization treatment in step 2 in a 0.05-0.5M phosphoric acid (H ₃ PO ₄ ) solution for 58-62 minutes.

In the manufacturing method according to the present invention, the electrolyte solution in which the first anodic oxidation in step 1, the second anodic oxidation in step 2, and the tertiary anodic oxidation in step 3 are performed are sulfuric acid (H ₂ SO ₄ ) and phosphoric acid, respectively. (phosphoric acid, H ₃ PO ₄ ), oxalic acid (C ₂ H2O ₄ ), chromic acid, hydrofluoric acid, or dipotassium phosphate (K ₂ HPO ₄ ) is used Or any one of these mixtures may be used, and the material on which the metal to be anodized is formed as a working electrode in the oxidation treatment reaction tank containing the electrolyte, and then an anode is applied, and then a platinum (Pt) or carbon electrode is applied. It may be formed by oxidation by applying a cathode as a counter electrode. Preferably, the electrolyte may be formed at a temperature of -5 to 10°C using 0.1-0.5M oxalic acid as an electrolyte, and more preferably at a temperature of 0.2-0.4M oxalic acid and -2 to 2°C. there is.

The 5000 series aluminum alloy is Al 5005, Al 5023, Al 5042, Al 5052, Al 5054, Al 5056, Al 5082, Al 5083, Al 5084, Al 5086, Al 5154, Al 5182, Al 5252, Al 5352, Al 5383 , Al 5454, Al 5456, Al 5457, Al 5657, Al 5754 and the like can be used.

In the manufacturing method according to the present invention, an anodized film having a Pillar-On-Pore structure is formed on the surface of the 5000 series aluminum alloy by the treatment of steps 1 to 4.

In the manufacturing method according to the present invention, the coating composition used in step 5 is 0.01-10 parts by weight of the cross-linked polydimethylsiloxane (PDMS) derivative represented by Formula 1, preferably 0.04-5 parts by weight, based on 10 parts by weight of the organic solvent. part, more preferably 0.04-3 parts by weight, more preferably 0.04-2 parts by weight, more preferably 0.04-1 parts by weight, particularly preferably 0.05-0.17 parts by weight.

If the content of the cross-linked PDMS derivative represented by Chemical Formula 1 is out of the above range, oil repellency and water repellency may decrease or the uniformity of the coating may be insufficient.

The coating composition according to the present invention is characterized in that it does not contain a PDMS (Polydimethylsiloxane) derivative represented by Formula 2 below.

[Formula 2]

(In Formula 2, m is an integer of 1-100, preferably an integer of 1-80, more preferably an integer of 1-60.)

The coating composition may be used by methods such as drop coating, dip coating, and spin coating, but is not limited thereto.

Among the organic solvents, hexane is used as an example in the present invention, but pentane, heptane, and octane may also be used.

In addition, the present invention provides a 5000 series aluminum alloy having an oil repellent and water repellent film produced by the above manufacturing method.

Furthermore, the present invention provides an oil vapor recovery device, a pipe, a hood, and a conduit including the 5000 series aluminum alloy on which the oil and water repellent films are formed.

In the method for producing an oil repellent and water repellent film on the surface of a 5000 series aluminum alloy according to the present invention, water repellency and oil repellency can be imparted by using the crosslinked PDMS derivative represented by Formula 1 and an organic solvent in a specific mixing ratio, and manufacturing The cost is low, and the thickness of the coating film can be adjusted from several to several tens of nm, so it can be applied to the coating of microstructured oxide films. Can be useful for conduits, etc.

1 is a scanning electron microscope photographing the three-dimensional structure of the top view and cross section of the aluminum alloy anodized film formed on the prepatterned aluminum alloy surface of Preparation Examples 1 to 4 according to the present invention ( SEM) images; At this time, MA was performed at 40V for 30 minutes, HA at 80V for 30 seconds, and PW at 30 ° C. for 30 minutes, and the scale bars of the surface and cross section are 200 nm and 1 μm, respectively.
Figure 2 is a scanning electron microscope (SEM) photographing the three-dimensional structure of the surface (top view) and cross section (cross view) of the aluminum alloy anodized film formed on the pre-patterned aluminum alloy surface of Production Examples 5 to 8 according to the present invention ( SEM) images; At this time, MA was performed at 40V for 30 minutes, HA at 80V for 30 seconds, and PW at 30 ° C. for 40 minutes, and the scale bars of the surface and cross section are 200 nm and 1 μm, respectively.
Figure 3 is a scanning electron microscope (SEM) photographing the three-dimensional structure of the surface (top view) and cross section (cross view) of the aluminum alloy anodized film formed on the surface of the pre-patterned aluminum alloy of Preparation Examples 9 to 12 according to the present invention ( SEM) images; At this time, MA was performed at 40V for 30 minutes, HA at 80V for 30 seconds, and PW at 30 ° C. for 50 minutes, and the scale bars of the surface and cross section are 200 nm and 1 μm, respectively.
Figure 4 is a scanning electron microscope (SEM) photographing the three-dimensional structure of the surface (top view) and cross section (cross view) of the aluminum alloy anodized film formed on the pre-patterned aluminum alloy surface of Production Examples 13 to 16 according to the present invention ( SEM) images; At this time, MA was performed at 40V for 30 minutes, HA at 80V for 30 seconds, and PW at 30 ° C. for 60 minutes, and the scale bars of the surface and cross section are 200 nm and 1 μm, respectively.
5 to 14 are results of measuring contact angles and contact hysteresis angles by coating the coating solutions of Examples 1 to 10 on aluminum 5052 alloy substrates not subjected to anodization treatment and then dropping water and oil.
15 is a result of measuring the contact angle and contact hysteresis angle by dropping water and oil on an aluminum 5052 alloy substrate (Comparative Example 1) without coating.
16 is a scanning electron microscope (SEM) image of a three-dimensional structure of a top view and a cross section of a POP type microstructured oxide film obtained by performing steps 1 to 4 in Preparation Example 16.
17 to 19 are coated with the coating solution of Examples 8 to 10 on an aluminum 5052 alloy substrate having a POP type microstructure oxide film formed by anodization, and then water and oil are dropped to measure the contact angle and contact hysteresis angle is a result
20 to 22 are samples prepared by coating the coating solutions of Examples 8 to 10 on an aluminum 5052 alloy substrate on which a POP type microstructured oxide film is formed obtained by anodization, and then scraping the sample surface with a tip. It is an image taken with a transmission electron microscope (TEM) and measuring the thickness of the coating film.

Hereinafter, the present invention will be described in more detail by the following examples. However, the following examples are merely illustrative of the present invention, and the contents of the present invention are not limited by the following examples.

<Manufacturing Example> Preparation of anodized film of Pillar-On-Pore (POP) structure through anodization of aluminum 5052 alloy

The following was carried out to find out the anodization treatment conditions in which a POP structure anodized film was formed on the surface of the aluminum 5052 alloy.

To prepare an aluminum alloy anodized film, pre-patterning, pore widening (PW), and voltage modulation were performed using an aluminum 5052 alloy. The component information of the aluminum 5052 alloy (Al 5052, size 20 × 30 mm) is as follows; Mg 2.2~2.8%, Si 0.25%, Fe 0.40%, Cu 0.10%, Mn 0.10%, Zn 1.0%, Cr 0.15~0.35% and Al Balance.

Step 1: Pre-patterning process through primary anodic oxidation and chemical etching

As a 5000 series aluminum (Al) alloy plate for producing anodized film, aluminum 5052 alloy (Alcoa INC, USA) was used, and ultrasonic treatment was performed in acetone and ethanol for 10 minutes to remove impurities on the surface of the aluminum 5052 alloy. and washed. In order to obtain surface roughness, the ultrasonically cleaned aluminum 5052 alloy was put into a mixed solution of ethanol and perchloric acid (Junsei, C ₂ H ₅ OH: HClO ₄ = 4: 1 (v / v)) at a voltage of 20 V at room temperature (20 ° C) was applied and electropolished for 1 minute. It was confirmed that the surface of the aluminum alloy after electropolishing was well reflected and the surface was flat.

The electropolished aluminum 5052 alloy (thickness 1 mm, size 20 × 30 mm) is used as a working electrode and a platinum (Pt) electrode is used as a cathode. Secondary anodization was performed. The primary anodic oxidation was performed using 0.3M oxalic acid as an electrolyte and maintaining a constant electrolyte temperature at 0° C. using a double beaker. It was stirred at a constant speed in order to suppress interference with stable oxide growth due to local temperature rise, and a voltage of 40V was applied using a constant voltage method to perform a primary anodization process for 6 hours to grow an alumina layer.

The alumina layer grown through the primary anodic oxidation treatment is immersed in a solution of chromic acid (1.8wt%) and phosphoric acid (6wt%) at 65° C. for 10 hours and then etched to remove the grown alumina layer. A pre-patterning process was performed.

Step 2-4: 2nd and 3rd anodic oxidation and pore expansion process

Specifically, in order to obtain a desired film structure on the surface of the aluminum 5052 alloy, after the pre-patterning was completed, secondary anodic oxidation, pore expansion, and tertiary anodic oxidation were performed.

Specifically, the second and third anodization processes of the embodiment were performed under the same acid electrolyte conditions as the first anodization process of step 1, and mild anodization (MA) using a relatively low voltage of 40V or 80V Anodization was performed by selectively adjusting the magnitude and order of voltages applied during secondary and tertiary anodization using two techniques of hard anodization (HA) using a high voltage of . At this time, soft anodization was performed at 40V for 30 minutes, and hard anodization was performed at 80V for 30 seconds. On the other hand, in the secondary and tertiary anodization processes of Preparation Examples 17 to 20, anodization was performed using super hard anodization (SA) conditions of voltage and time as shown in Table 1 below.

In addition, the alumina layer grown through the secondary anodic oxidation is immersed in a 0.1M phosphoric acid solution at 30 ° C. for 30 to 60 minutes before performing the tertiary anodic oxidation, followed by a pore widening (PW) process, A third anodic oxidation was performed to grow an aluminum anodic oxide film.

Secondary anodization (step 2), pore expansion (step 3), and third anodization (step 4) processes were performed under the conditions shown in Table 1 below to control the structural shape of the aluminum 5052 alloy surface. A coating was obtained.

process mode
(steps 2-4) 2nd anodic oxidation
(Step 2) stomatal expansion (step 3) 3rd anodic oxidation
(Step 4) Voltage (V) time (min) time (min) Voltage (V) time (min) Preparation Example 1 MA→PW→MA 40 30 30 40 30 Preparation Example 2 MA→PW→HA 40 30 30 80 0.5 Preparation Example 3 HA→PW→MA 80 0.5 30 40 30 Production Example 4 HA→PW→HA 80 0.5 30 80 0.5 Preparation Example 5 MA→PW→MA 40 30 40 40 30 Preparation Example 6 MA→PW→HA 40 30 40 80 0.5 Preparation Example 7 HA→PW→MA 80 0.5 40 40 30 Preparation Example 8 HA→PW→HA 80 0.5 40 80 0.5 Preparation Example 9 MA→PW→MA 40 30 50 40 30 Preparation Example 10 MA→PW→HA 40 30 50 80 0.5 Preparation Example 11 HA→PW→MA 80 0.5 50 40 30 Preparation Example 12 HA→PW→HA 80 0.5 50 80 0.5 Preparation Example 13 MA→PW→MA 40 30 60 40 30 Preparation Example 14 MA→PW→HA 40 30 60 80 0.5 Preparation Example 15 HA→PW→MA 80 0.5 60 40 30 Preparation Example 16 HA→PW→HA 80 0.5 60 80 0.5

<Experimental Example 1> Analysis of structural characteristics of aluminum alloy anodized film according to secondary and tertiary anodic oxidation conditions (voltage and time) and pore expansion time

As shown in Table 1, Preparation Examples 1 to 16 prepared by performing various modes of MA→PW→MA, MA→PW→HA, HA→PW→HA and HA→PW→MA and varying the pore expansion time The surface and cross-sectional morphology of the porous aluminum alloy anodized film were observed using a field emission scanning electron microscope (FE-SEM) system (AURIGA® small dual-bean FIB-SEM, Zeiss).

Each aluminum alloy anodized film specimen was cut into small pieces, fixed on a stage with carbon tape, coated with gold (Au) for 15 seconds by sputtering, and then imaged with a scanning electron microscope (SEM). At this time, the film specimen was bent at 90 ° to create parallel cracks, and the surface and cross-sectional structure of the aluminum alloy anodized film were observed and shown in FIGS. 1 to 4.

1 to 4 are top views and cross-sections of aluminum alloy anodized films formed on pre-patterned aluminum alloy surfaces of Preparation Examples 1 to 4, 5 to 8, 9 to 12, and 13 to 16 according to the present invention, respectively. This is a scanning electron microscope (SEM) image of a three-dimensional structure of (cross view); At this time, MA was performed at 40 V for 30 minutes, HA at 80 V for 30 seconds, and PW at 30 ° C. for 30 to 60 minutes, and the scale bars of the surface and cross section are 200 nm and 1 μm, respectively.

As shown in FIGS. 1 to 4, in most cases, the PW process resulted in an increase in the diameter of pores in the secondary anodization region of the aluminum alloy anodization film, but the structure of the third anodization region did not affect Therefore, since the size of the pores in the second and third anodization regions of Preparation Examples 1 to 16 is different, the second and third anodization regions can be classified according to the pore size transition.

In addition, it was found that the pore diameter and the distance between pores and pores were greater in the anodic oxide film containing HA as the voltage type than that of the anodic oxide film as the voltage type containing MA. From these results, it was confirmed that the size of the anodic oxidation voltage can affect the size of pores.

On the other hand, as shown in Figures 3 and 4, in the case of Preparation Examples 12 and 16 prepared by performing PW for 50 minutes or 60 minutes in the HA→PW→HA mode, the lower part in the cross-view image It was confirmed that aligned linear pores were formed in the tertiary anodic oxidation region and a tip-like structure was formed in the secondary anodic oxidation region on the linear pore. The top view image shows that white (light gray) anodic oxide is formed next to the black pores, and the corresponding portion is a tip-like structure portion formed in the secondary anodic oxidation region. Confirmed.

Therefore, in Preparation Examples 12 and 16, unlike other Preparation Examples, an anodized film having a Pillar-On-Pore structure in which bundle-shaped pillars are formed on the porous structure is manufactured. It was confirmed that it was, and in particular, when prepared under the conditions of Preparation Example 16, it was confirmed that it exhibited a much clearer pillar-on-pore form.

As a result, the size of the secondary and tertiary anodization voltages, which are parameters, have a direct effect on the size of pores, controlling the diameter of pores and the spacing between pores and pores, as well as the growth of three-dimensional aluminum anodized films. It was confirmed that the can be controlled, and in particular, the HA (80V, 30sec) → PW (60min) → HA (80V, 30sec) conditions of Preparation Example 16 are the conditions for producing an anodized film with the clearest POP structure. Confirmed.

<Example> Preparation of aluminum 5052 alloy imparting water and oil repellency

As an example of the metal substrate, aluminum 5052 alloy not treated with anodization was used as the substrate to be coated.

Step 1: Plasma treatment

The substrate was treated with plasma for 15 minutes under conditions of 200 W, 50 kHz, and O ₂ : 50 sccm. In Examples 1 to 6, the plasma treatment of step 1 was performed, and in Examples 7 to 10, the plasma treatment was not performed.

Step 2: Removal of impurities through heat treatment

The substrate subjected to plasma treatment in step 1 was heat treated in an oven at 150° C. for 10 minutes to remove impurities. On the other hand, this step 2 was also performed on the samples of Examples 7 to 10 that were not subjected to plasma treatment.

Step 3: Coating of the coating agent

SYLGARD 184 Silicon Elastomer Curing Agent (manufacturer: Dow chemical company), a cross-linked PDMS derivative represented by Formula 1, and SYLGARD 184 Silicon Elastomer Base, a PDMS derivative represented by Formula 2, as coating agents on the substrate from which impurities are removed in step 2. Manufacturer: Dow chemical company) and/or 60 μL of hexane per 2.5 cm × 3 cm area of the substrate, and then coated by spin coating (corresponding to Examples 2, 4 and 6-7). Spin coating was performed at 1000 rpm for 30 seconds. In addition, drop coating was performed by another coating method (corresponding to Examples 1, 3, 5 and 8-10). In the case of drop coating, an appropriate amount of the coating agent was dropped, and then the substrate was tilted from side to side several times for coating.

In Examples 1-4, hexane, a main agent (Formula 2) and a curing agent (Formula 1) were mixed and used as a coating agent,

In Examples 5-10, hexane and a curing agent (Formula 1) were mixed and used as a coating agent.

Step 4: Hardening through heat treatment

The substrate coated in step 3 was heat treated in an oven at 300° C. for 30 minutes to complete curing.

Example plasma
Processing Coating agent composition (weight ratio) coating
method coating liquid
usage
(μL/7.5 cm ² ) hexane coating agent
(Sylgard 184) Base
(subject) Curing agent
(curing agent) One ○ 10 One 0.1 drop 65 2 ○ 10 One 0.1 spin 65 3 ○ 10 2 0.2 drop 65 4 ○ 10 2 0.2 spin 65 5 ○ 10 0 One drop 65 6 ○ 10 0 One spin 65 7 × 10 0 One spin 65 8 × 10 0 One drop 85 9 × 10 0 0.5 drop 85 10 × 10 0 0.1 drop 85

[Formula 1: Curing agent]

In Formula 1, x and y are each an integer of 1-30.

[Formula 2: Base]

In Formula 2, m is an integer of 1-100.

For reference, examples in which coating was performed using an anodized aluminum 5052 alloy as a substrate are described in Experimental Examples 3 to 5 to be described later.

<Comparative Example 1> Preparation of anodized non-anodized aluminum 5052 alloy substrate

A sample without coating was prepared as Comparative Example 1 on a non-anodized aluminum 5052 alloy substrate.

<Comparative Example 2> Preparation of substrate coated with SAM on anodized aluminum 5052 alloy substrate

A sample obtained by applying SAM (Self-Assembled Monolayer) coating on an aluminum 5052 alloy substrate on which a POP (Pillar-On-Pore) microstructure oxide film was formed through anodization was prepared as Comparative Example 2.

Steps 1 to 4:

Steps 1 to 4 were performed in the same manner as in Preparation Example 16 to prepare an aluminum 5052 alloy substrate having a POP microstructure oxide film (see FIG. 16).

Step 5: Hydrophobic film formation through SAM coating

The aluminum 5052 alloy substrate on which the POP type microstructured oxide film obtained in step 4 was formed was coated with 1H, 1H, 2H, 2H-perfluorodecyltrichlorosilane (FDTS), a coating material with low surface energy, in a vacuum chamber for 24 hours. SAM (Self-Assembled Monolayer) By coating, a hydrophobic film was formed.

<Experimental Example 2> Evaluation of coating properties (uniformity and cracking)

In order to evaluate the coatability of the samples prepared in Examples 1 to 10, the uniformity of the coating and the cracking of the coating were evaluated.

coating uniformity
(4>3>2>1 point in uniform order) cracked coating
(4>3>2>1 point in order of no cracks) Example 1 2 points 1 point Example 2 2 points 1 point Example 3 1 point 1 point Example 4 1 point 1 point Example 5 4 points 4 points Example 6 4 points 4 points Example 7 4 points 4 points Example 8 4 points 4 points Example 9 4 points 4 points Example 10 4 points 4 points

As shown in Table 3, it can be seen that the samples of Examples 5 to 10 are excellent in that the coating properties of the samples having excellent coating uniformity (4 points) and no cracking (4 points) are the best. there was.

<Experimental Example 3> Evaluation of water repellency and oil repellency

(1) Substrates not treated with anodization (Examples 1 to 10)

With respect to the samples coated with the coating solutions of Examples 1 to 10 based on the aluminum 5052 alloy not subjected to anodization, water (purified water) and oil (edible oil) were dropped to evaluate the contact angle and contact hysteresis angle, respectively. , The results are shown in FIGS. 5 to 15, and the results of FIGS. 5 to 15 are summarized and shown in Table 4 below. Comparative Example 1 is a sample in which the aluminum 5052 alloy was not treated with a coating solution.

Here, the 'contact angle hysteresis' refers to placing a sample on a stage of a device whose inclination can be finely adjusted, dropping water or oil on the sample, and then gradually adding the inclination to the stage, and allowing the water or oil to flow. It measures the angle of inclination at which it begins to descend. That is, the lower the contact hysteresis angle, the better the water/oil repellency. For example, when the contact hysteresis angle is 1°, water or oil flows down even when the sample is tilted by only 1°, and when the contact hysteresis angle is 90°, water or oil does not flow down even when the sample is stood at 90°.

Table 4 below shows the results of evaluation of water repellency and oil repellency after coating the coating solution according to the example on a substrate on which a microstructured oxide film is not formed on the surface of an aluminum 5052 alloy substrate untreated by anodization.

Non -anodized substrate water oil Contact angle (0 sec) contact hysteresis angle Contact angle (60 seconds) contact hysteresis angle Example 1 107.59±1.31° 29.11±0.44° 60.56±0.43° 25.74±0.41° Example 2 104.57±0.35° 25.65±0.58° 61.05±0.67° 26.95±0.64° Example 3 99.57±0.22° 27.43±0.75° 57.05±1.05° 27.56±0.37° Example 4 100.28±1.24° 27.91±0.94° 54.87±1.44° 27.79±0.09° Example 5 102.66±0.80° 22.20±0.58° 60.79±1.38° 22.12±0.37° Example 6 100.87±3.00° 28.32±0.85° 58.44±6.00° 28.52±2.90° Example 7 103.96±2.83° 24.19±0.24° 59.62±1.43° 24.86±1.40° Example 8 114.13±2.53° 20.07±0.41° 58.84±3.10° 20.60±0.20° Example 9 113.22±1.47° 19.94±2.20° 54.55±8.12° 13.75±1.02° Example 10 114.63±0.18° 13.66±0.42° 55.01±2.48° 10.65±0.92° Comparative Example 1
(Uncoated) 77.72±4.64° 41.26±4.31° 31.67±6.02° 33.57±0.68°

As shown in Table 4, the contact hysteresis angles of Examples 8 to 10 were the lowest, confirming that the water repellency/oil repellency was excellent. On the other hand, no significant improvement in water repellency/oil repellency was observed with or without plasma pretreatment.

(2) Substrates having a microstructured oxide film formed through anodic oxidation treatment (Examples 8A to 10A)

Based on the aluminum 5052 alloy obtained by performing steps 1 to 4 in Preparation Example 16 and having an oxide film in the form of a POP microstructure by anodizing, the samples coated with the coating solutions of Examples 8 to 10 were treated with water (Purified water) and oil (edible oil) were dropped to evaluate the contact angle and contact hysteresis angle, and the results are shown in FIGS. 17 to 19, and the results of FIGS. 17 to 19 are summarized in Table 5 below.

Table 5 below is an anodized sample of an aluminum 5052 alloy substrate having a pillar on pore (POP) type microstructured oxide film formed on the surface thereof, coated with the coating solution according to Examples 8 to 10, and then evaluated for water repellency and oil repellency. This is the result. Here, when a metal substrate is anodized to form a POP-type microstructure on the surface, a super-hydrophilic oxide film is formed. When the microstructure is maintained by applying a hydrophobic coating with a thin thickness, superhydrophobicity can be realized.

Anodized substrate water oil Contact angle (0 sec) contact hysteresis angle Contact angle (60 seconds) contact hysteresis angle Example 8A 114.18±1.56° 16.71±0.74° 68.98±0.56° 3.72±0.09° Example 9A 116.22±1.15° 15.42±0.04° 69.44±0.03° 2.67±0.41° Example 10A 170.51±2.45° 3.82±0.67° 74.20±7.02° 1.08±0.16° Comparative Example 2
(FDTS coating) 170.40±0.05° 3.91±0.08° 45.56±2.36° 69.54±0.19°

As shown in Table 5, all of Examples 8A to 10A showed excellent water repellency and oil repellency. In particular, in the case of Example 10A, water repellency and oil repellency were surprisingly excellent. This is because the coating solution of Example 10 had a low content of the curing agent represented by Formula 1, so that the thickness of the formed coating film was similar to that of a monomolecular film, from several to several tens of nm. It is thought that this is an effect of maintaining the microstructure of the oxide film.

Here, in a substrate on which a POP type microstructured oxide film is formed through anodization, the diameter of pores in the POP microstructure is approximately 200 nm (see FIG. 12), and the thickness of the coating film must be as thin as several to several tens of nm to form an oxide film It is possible to maintain the form of the microstructure formed in, and when the thickness of the coating film exceeds the level of hundreds of nm, the shape of the microstructure disappears and the coating film is coated flatly, so that the effect according to the microstructure is lost.

From this point of view, Comparative Example 2 is a sample in which superhydrophobicity is formed by coating FDTS as a hydrophobic SAM (Self-Assembled Monolayer) coating agent sold at a high price on a POP type microstructured oxide film, and has excellent water repellency. The FDTS coating agent is too expensive and cannot be applied to a large-area metal substrate. In addition, in the case of the FDTS coating agent, oil repellency is hardly shown.

However, the coating solution according to the present invention not only uses the curing agent represented by Chemical Formula 1, which is significantly cheaper than the SAM coating agent, but also contains only 0.1 part by weight of the curing agent represented by Chemical Formula 1 based on 10 parts by weight of hexane solvent based on Example 10. It can be produced very cheaply, and it can produce a similar level of water repellency as the SAM coating agent, but also can produce a remarkable effect in oil repellency.

In the following Experimental Example 4, the thickness of the coating film formed when the substrate was coated using the coating solutions of Examples 8 to 10 was evaluated.

<Experimental Example 4> Coating film thickness evaluation

After preparing a sample coated with the coating solution according to Examples 8 to 10 on a substrate having a POP (pillar on pore) type microstructure oxide film formed on the surface as an anodized sample of an aluminum 5052 alloy substrate, the sample surface was scraped with a tip The obtained sample was measured by TEM to measure the thickness of the formed coating film, and the results are shown in FIGS. 20 to 22.

20 to 22 are samples prepared by coating the coating solutions of Examples 8 to 10 on an aluminum 5052 alloy substrate on which a POP type microstructured oxide film is formed obtained by anodization, and then scraping the sample surface with a tip. It is an image taken with a transmission electron microscope (TEM) and measuring the thickness of the coating film.

20 to 22, the lower the content of the curing agent represented by Formula 1, the thinner the coating thickness. The coating film thickness of Examples 8A to 9A was approximately 150-180 nm, and in particular, the coating film thickness of Example 10A was approximately 15 nm, confirming that the coating thickness was similar to that of the SAM coating agent.

<Experimental Example 5> Derivation of optimal blending ratio of crosslinked PDMS derivative of Formula 1 and hexane suitable for coating on a substrate having a microstructured oxide film

Through the results of Experimental Examples 2 to 4, it was confirmed that the sample of Example 10 had excellent coating properties, remarkably excellent water repellency and oil repellency, and formed a coating film thickness thin enough to maintain the microstructure.

Accordingly, in Experimental Example 5, a contact hysteresis angle experiment was conducted in the same manner as in Experimental Example 3 in order to derive an optimal mixing ratio of the crosslinked PDMS derivative of Chemical Formula 1 and hexane suitable for coating on a substrate having a microstructured oxide film.

In Table 6, the curing agent and hexane of the coating agent were measured and indicated by weight ratio, and the substrate was an aluminum 5052 alloy having a POP type microstructure oxide film obtained by performing steps 1 to 4 of Preparation Example 16, Example 10 and Similarly, the sample was prepared by drop coating without plasma treatment.

Example Coating agent mixing weight ratio Contact hysteresis angle (°) hexane curing agent
(Formula 1) water oil 10-1 10 0.01 18.22±0.59 4.62±0.66 10-2 10 0.03 17.66±0.88 4.25±0.57 10-3 10 0.05 4.03±0.55 1.13±0.23 10-4 10 0.07 3.98±0.47 1.09±0.28 10-5 10 0.1 3.82±0.67 1.08±0.16 10-6 10 0.13 3.91±0.54 1.11±0.22 10-7 10 0.15 3.89±0.12 1.10±0.41 10-8 10 0.17 3.95±0.26 1.12±0.58 10-9 10 0.20 14.87±0.59 2.53±0.87

As shown in Table 6, in Examples 10-3 to 10-8, the coating film thickness was formed thin enough to maintain the microstructure, and the coating film was formed uniformly over the entire substrate, showing significantly excellent water and oil repellency. I was able to confirm. On the other hand, in the case of Examples 10-1 and 10-2, the content of the curing agent is too low, so it is expected that the coating film is not formed on a part of the substrate, and in the case of Example 10-9, the content of the curing agent is too high, so it is too thick to maintain the microstructure. It is expected that a coating film is formed.

So far, the present invention has been looked at with respect to its preferred embodiments. Those skilled in the art to which the present invention pertains will be able to understand that the present invention can be implemented in a modified form without departing from the essential characteristics of the present invention. Therefore, the disclosed embodiments should be considered from an illustrative rather than a limiting point of view. The scope of the present invention is shown in particular in the claims rather than the foregoing description, and all differences within the equivalent range will be construed as being included in the present invention.

Claims (15)

A pre-patterning step (step 1) of first anodizing a 5000 series aluminum alloy at 30-50V for 5-15 hours and then etching to remove the first anodized film;
Secondary anodic oxidation treatment of the 5000 series aluminum alloy for which pre-patterning has been completed in step 1 at 75-85V for 25-35 seconds (step 2);
pore widening by immersing the 5000 series aluminum alloy subjected to secondary anodization in step 2 in a 0.05-1.0M phosphoric acid (H ₃ PO ₄ ) solution for 55-65 minutes (step 3);
subjecting the 5000 series aluminum alloy to which the pore expansion was completed in step 3 at 75-85V for 25-35 seconds (step 4); and
Coating with a coating composition containing a cross-linked polydimethylsiloxane (PDMS) derivative represented by Formula 1 and an organic solvent (step 5); including,
Manufacturing method of oil repellent and water repellent film on the surface of 5000 series aluminum alloy.
[Formula 1]

(In Formula 1, x and y are each an integer of 1-30.)
According to claim 1,
A manufacturing method characterized in that a 5000 series aluminum alloy anodized film having a surface of a Pillar-On-Pore structure is formed through the steps 1 to 4.
According to claim 1,
The 5000 series aluminum alloy is Al 5005, Al 5023, Al 5042, Al 5052, Al 5054, Al 5056, Al 5082, Al 5083, Al 5084, Al 5086, Al 5154, Al 5182, Al 5252, Al 5352, Al 5383 , A manufacturing method characterized in that at least one selected from the group consisting of Al 5454, Al 5456, Al 5457, Al 5657 and Al 5754.
According to claim 1,
The organic solvent in step 5 is a manufacturing method, characterized in that one of pentane, hexane, heptane and octane.
According to claim 1,
The coating composition used in step 5 is
Based on 10 parts by weight of organic solvent,
A manufacturing method characterized in that it comprises 0.01-10 parts by weight of the cross-linked PDMS (Polydimethylsiloxane) derivative represented by Formula 1.
According to claim 5,
The coating composition used in step 5 is
Based on 10 parts by weight of organic solvent,
A manufacturing method characterized in that it comprises 0.04-5 parts by weight of the cross-linked PDMS (Polydimethylsiloxane) derivative represented by Formula 1.
According to claim 6,
The coating composition used in step 5 is
Based on 10 parts by weight of organic solvent,
A manufacturing method comprising 0.04-2 parts by weight of a cross-linked PDMS (Polydimethylsiloxane) derivative represented by Formula 1.
According to claim 7,
The coating composition used in step 5 is
Based on 10 parts by weight of organic solvent,
A manufacturing method characterized in that it comprises 0.04-1 parts by weight of the cross-linked PDMS (Polydimethylsiloxane) derivative represented by Formula 1.
According to claim 8,
The coating composition used in step 5 is
Based on 10 parts by weight of organic solvent,
A manufacturing method characterized in that it comprises 0.05-0.17 parts by weight of the cross-linked PDMS (Polydimethylsiloxane) derivative represented by Formula 1.
According to claim 1,
A manufacturing method characterized in that the coating composition used in step 5 does not contain a polydimethylsiloxane (PDMS) derivative represented by the following formula (2).
[Formula 2]

(In Formula 2, m is an integer of 1-100.)
A 5000 series aluminum alloy having an oil repellent and water repellent film produced by the manufacturing method of claim 1.
An oil vapor recovery device comprising a 5000 series aluminum alloy having the oil and water repellent film of claim 11 formed thereon.
A pipe comprising a 5000 series aluminum alloy having the oil and water repellent film of claim 11 formed thereon.
A hood comprising a 5000 series aluminum alloy having the oil and water repellent film of claim 11 formed thereon.
A pipe line comprising a 5000 series aluminum alloy having the oil and water repellent film of claim 11 formed thereon.

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