KR20170024377A - Ceramic hybrid coating film, ceramic hybrid multi-layer coating film, method for preparing the same, and head lamp for automobile including the same - Google Patents
Ceramic hybrid coating film, ceramic hybrid multi-layer coating film, method for preparing the same, and head lamp for automobile including the same Download PDFInfo
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- B—PERFORMING OPERATIONS; TRANSPORTING
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- B60Q—ARRANGEMENT OF SIGNALLING OR LIGHTING DEVICES, THE MOUNTING OR SUPPORTING THEREOF OR CIRCUITS THEREFOR, FOR VEHICLES IN GENERAL
- B60Q1/00—Arrangement of optical signalling or lighting devices, the mounting or supporting thereof or circuits therefor
- B60Q1/02—Arrangement of optical signalling or lighting devices, the mounting or supporting thereof or circuits therefor the devices being primarily intended to illuminate the way ahead or to illuminate other areas of way or environments
- B60Q1/04—Arrangement of optical signalling or lighting devices, the mounting or supporting thereof or circuits therefor the devices being primarily intended to illuminate the way ahead or to illuminate other areas of way or environments the devices being headlights
- B60Q1/06—Arrangement of optical signalling or lighting devices, the mounting or supporting thereof or circuits therefor the devices being primarily intended to illuminate the way ahead or to illuminate other areas of way or environments the devices being headlights adjustable, e.g. remotely-controlled from inside vehicle
- B60Q1/08—Arrangement of optical signalling or lighting devices, the mounting or supporting thereof or circuits therefor the devices being primarily intended to illuminate the way ahead or to illuminate other areas of way or environments the devices being headlights adjustable, e.g. remotely-controlled from inside vehicle automatically
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- C01B—NON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
- C01B33/00—Silicon; Compounds thereof
- C01B33/113—Silicon oxides; Hydrates thereof
- C01B33/12—Silica; Hydrates thereof, e.g. lepidoic silicic acid
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- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
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Abstract
0.0005 to 15% by weight of reduced graphene oxide (RGO); 0.001 wt% to 10 wt% of at least one hydrophilic hydrate represented by the formula (1) or at least one hydrophobic hydrate represented by the formula (2); 0.02% to 20% by weight of silica nanoparticles; And a graft-containing ceramic hybrid sol solution containing a residual amount of a hydrophilic solvent,
The ceramic hybrid coating film has a water droplet contact angle of 20 DEG or less, or 60 DEG or more, a ceramic hybrid multilayer coating film containing the same, and a method of manufacturing the same.
The description of the above Formulas 1 and 2 is as described in the present specification.
Description
The present invention relates to a ceramic hybrid coating film, a ceramic hybrid multilayer coating film, a manufacturing method thereof, and an automobile headlamp including the same.
Generally, the surface of a solid such as a metal, a ceramic, or a polymer has a surface energy inherent to the material, and when the liquid such as water or oil is buried on the surface, the contact angle between the solid surface and the liquid reflects the surface energy thereof . When the contact angle is 20 ° or less, the liquid exhibits hydrophilicity and excellent wettability that spreads on the surface thereof and makes the surface wet with the liquid. When the angle is 60 ° or more, spherical liquid droplets do not wet the solid surface, Water repellency.
Particularly, when the contact angle is 5 ° or less, the superhydrophilic property is obtained.
On the other hand, graphene oxide (graphite oxide, graphite oxide, hereinafter referred to as GO) is a plate-shaped carbon material produced by acid treatment of graphite, and has a large amount of hydrophilic functional group, carboxyl group (-COOH), hydroxyl group ). GO is prepared in the form of a hydrate form or a water-containing slurry in which the surface oxidation groups generated through an acid treatment process naturally form hydrogen bonds with H 2 O. Generally, the solid content concentration of such a slurry is about 2 to 8% by weight, unless subjected to special treatment.
The GO improves the strength and has appropriate thermal conductivity when contained in a film or a structure, but treatment of the contained GO is a great obstacle to the manifestation of physical properties.
Generally, the GO is manufactured in a graphene form through a chemical reduction process (hydrazine process, etc.) and a heat reduction process, and is used widely. At this time, the reduced graphene is called Reduced Graphene Oxide (RGO).
It has been proven that some of the oxidizing groups on the RGO surface can not be completely removed and the oxygen content by the surface oxidizing group is usually 5 wt% or less with respect to the carbon backbone, so that the graphene (RGO) Means that the oxygen content by the oxidizing agent is 5% by weight or less based on the carbon backbone.
Recently, the properties of GO and RGO have been attracting much attention because of the possibility of improving the physical properties through the synergy effect between the materials beyond the limit of existing materials. Typical examples of the high-strength composite material and the fuel cell include graphene-nanowire (semiconductor) hybrid structures (KR2011-0012479), which generate electron-hole pairs by absorbing light energy on the upper portion of the graphene conductive portion, pin sheet / CNT / method of manufacturing a hybrid composite including a polymeric nanoparticles (KR2010-0114646), yes by the addition of Fe precursor and PO 4 precursor to the pin method of producing a cathode material for a lithium secondary battery, the hybrid material (KR2010- (US Pat. No. 8,257,867), a method of producing a graphene composite sintered body having excellent charging / discharging rates by sintering graphene and metal oxide particles in air (US Pat. No. 8,257,867), graphene-TiO 2 2 hybrid material manufacturing method (US2011-986379), and a graphene ceramic composite manufacturing method (10-2012-0039799, 10-2013-0014327).
In addition, JP-A-2001-0039799 discloses a technique of chemically bonding a ceramic precursor directly to a carboxyl group (-COOH) at the edge of the GO to improve dispersibility, thereby improving the coating property of the graphene itself. Although the graphene itself is coated with a chemical bond at the edge of the GO, a high electrical conductivity can be induced, but there is no binder between the GO and the graphene layer to be coated. Open patent application KR10-2013-0014327 discloses a method of making a graphene complex by mixing a ceramic precursor in the form of a salt (SALT such as chloride) with graphene or graphene oxide and calcining at high temperature. However, when a direct chemical bond is formed between the ceramic and the graphene, the plate-like structure of the graphene itself is broken and the inherent physical properties of the graphene are lost.
This problem is particularly serious when the ceramic is an oxide because the carbon component of graphene bonds with the oxygen component of the ceramic and is released as a gas in the form of CO 2 and CO 2 , and the residues are fragmented like carbon waste. Similar problems arise when the oxide ceramic precursor, or oxide ceramic sol, is calcined with graphene.
Further, when the graphene is reacted at a low temperature at which the graphene does not react with oxygen in order to reduce the above problems, there is a problem that the interface between the oxide ceramics and the graphene is extremely poor and peeling occurs. That is, the hydrophobicity of graphene and the hydrophilicity of ceramic.
In general, when a ceramic film is prepared by coating a ceramic sol with gelation, there is a problem that the membrane is collapsed due to evaporation of the solvent and osmotic pressure during the drying process. In addition, when the graphene is introduced into the ceramic film, And the prevention of drying (the problem that the graphene layer is located on the surface, the movement of the solvent is prevented and diffusion is prevented and the drying becomes non-uniform), it is actually a difficult technique to produce a hybrid film containing graphene at an appropriate concentration.
From the practical commercialization point of view, graphene is uniformly dispersed in one layer so as not to bend in the solid phase matrix, and the problem of manifesting the physical properties of the graphene-containing composite is overlooked, and no concrete process examples are presented.
As a technique for solving the above problems, there have been proposed methods for producing a composite powder or a composite membrane by applying a method of reducing a metal precursor at room temperature to powder, a plating method, and a sputtering method to graphene. The use of the entire amount of polymer resin is the most common.
However, the dispersibility of the graphene composite materials is very poor, and the resin has a disadvantage of drastically lowering thermal conductivity and film durability of graphene.
In the present invention, there is a problem that graphene is highly dispersed in forming a graphene-containing coating film, a problem of interfacial bonding between highly dispersed graphene and solid matrix, heat treatment in the state of containing oxide ceramics, And to provide a coating film having physical properties such as a functional coating film in which the function of graphene is expressed, a coating film having excellent thermal conductivity, superhydrophilic property, and super water repellency.
One embodiment of the present invention is a coating composition comprising 0.0005 to 15% by weight of a reduced graphene oxide (RGO); 0.001 to 10% by weight of at least one hydrophilic silane hydrate represented by the following formula (1) or at least one hydrophobic silane hydrate represented by the following formula (2); 0.02 to 20% by weight of silica nanoparticles; And a graft-containing ceramic hybrid sol solution containing a residual amount of a hydrophilic solvent,
The ceramic hybrid coating film has a water droplet contact angle of 20 DEG or less, or 60 DEG or more.
[Chemical Formula 1]
X a n -M- (OH) 4-n
(2)
X b n -M- (OH) 4-n
In the above Formulas 1 and 2,
M is selected from Si, Ti, Ag, Sn, In, Zn, and combinations thereof,
X a represents an epoxy group, a glycidoxy group, a carboxyl group, an amino group, an azo group, an azo group, an ureido group, an isocyanate group, an oxyimino group, a morpholinyl group, a piperazinyl group, a fluoro group, a chloro group, , A C1 to C30 alkyl group substituted or unsubstituted with at least one functional group selected from a hydroxyl group, a C1 to C10 alkoxy group, a C1 to C10 ketone group, a C1 to C10 amine group, and a C1 to C10 ester group;
An amino group, an azine group, an azo group, an ureido group, an isocyanate group, an oxyimino group, a morpholinyl group, a piperazinyl group, a fluoro group, a chloro group, a bromo group, an iodo group, a hydroxy group, A C1 to C30 alkenyl group substituted or unsubstituted with at least one functional group selected from a C1 to C10 alkoxy group, a C1 to C10 ketone group, a C1 to C10 amine group, and a C1 to C10 ester group;
An amino group, an azine group, an azo group, an ureido group, an isocyanate group, an oxyimino group, a morpholinyl group, a piperazinyl group, a fluoro group, a chloro group, a bromo group, an iodo group, a hydroxy group, A C1 to C30 alkynyl group substituted or unsubstituted with at least one functional group selected from a C1 to C10 alkoxy group, a C1 to C10 ketone group, a C1 to C10 amine group, and a C1 to C10 ester group; or
An amino group, an azine group, an azo group, an ureido group, an isocyanate group, an oxyimino group, a morpholinyl group, a piperazinyl group, a fluoro group, a chloro group, a bromo group, an iodo group, a hydroxy group, A C3 to C10 cycloalkyl group which is unsubstituted or substituted with at least one functional group selected from a C1 to C10 alkoxy group, a C1 to C10 ketone group, a C1 to C10 amine group, and a C1 to C10 ester group,
X b is a C1 to C30 alkyl group substituted or unsubstituted with at least one functional group selected from a vinyl group, an acryl group, a methacryl group, a thiol group, a mercapto group, a C1 to C10 sulfur group, and a C6 to C20 aryl group ;
A C1 to C30 alkenyl group substituted or unsubstituted with at least one functional group selected from a vinyl group, an acryl group, a methacryl group, a thiol group, a mercapto group, a C1 to C10 sulfur group, and a C6 to C20 aryl group;
A C1 to C30 alkynyl group substituted or unsubstituted with at least one functional group selected from a vinyl group, an acrylic group, a methacrylic group, a thiol group, a mercapto group, a C1 to C10 sulfur group, and a C6 to C20 aryl group; or
A C3 to C10 cycloalkyl group which is substituted or unsubstituted with at least one functional group selected from a vinyl group, an acryl group, a methacryl group, a thiol group, a mercapto group, a C1 to C10 sulfur group, and a C6 to C20 aryl group,
n is an integer of 1 to 3;
0.001 to 10% by weight of the graphene oxide (RGO), and 0.001 to 10% by weight of the hydrophilic hydrate represented by the formula (1), wherein the ceramic hybrid coating film The water droplet contact angle may be 12 degrees or less.
0.001 to 10% by weight of the graphene oxide (RGO), and 0.001 to 10% by weight of the hydrophobic hydrate of the formula (2), wherein the ceramic hybrid coating film The contact angle of the water droplet may be 90 ° or more.
The average diameter of the silica nanoparticles may be between 5 nm and 30 nm.
The formula (1) is represented by any one of the following formulas (1-1) to (1-3)
The formula (2) may be represented by any one of the following formulas (2-1) to (2-3).
[Formula 1-1]
X 1 -M- (OH) 3
[Formula 1-2]
X 1 X 2 -M- (OH) 2
[Formula 1-3]
X 1 X 2 X 3 -M- (OH)
[Formula 2-1]
X 4 -M- (OH) 3
[Formula 2-2]
X 5 X 6 -M- (OH) 2
[Formula 2-3]
X 7 X 8 X 9 -M- (OH)
In Formulas 1-1 to 1-3, and 2-1 to 2-3,
M is selected from Si, Ti, Ag, Sn, In, Zn, and combinations thereof,
X 1 to X 3 each independently represent an epoxy group, a glycidoxy group, a carboxyl group, an amino group, an azo group, an azo group, an ureido group, an isocyanate group, an oxyimino group, a morpholinyl group, a piperazinyl group, Substituted with at least one functional group selected from the group consisting of a halogen atom, a cyano group, a bromo group, an iodine group, a hydroxy group, a C1 to C10 alkoxy group, a C1 to C10 ketone group, a C1 to C10 amine group, C30 alkyl group;
An amino group, an azine group, an azo group, an ureido group, an isocyanate group, an oxyimino group, a morpholinyl group, a piperazinyl group, a fluoro group, a chloro group, a bromo group, an iodo group, a hydroxy group, A C1 to C30 alkenyl group substituted or unsubstituted with at least one functional group selected from a C1 to C10 alkoxy group, a C1 to C10 ketone group, a C1 to C10 amine group, and a C1 to C10 ester group;
An amino group, an azine group, an azo group, an ureido group, an isocyanate group, an oxyimino group, a morpholinyl group, a piperazinyl group, a fluoro group, a chloro group, a bromo group, an iodo group, a hydroxy group, A C1 to C30 alkynyl group substituted or unsubstituted with at least one functional group selected from a C1 to C10 alkoxy group, a C1 to C10 ketone group, a C1 to C10 amine group, and a C1 to C10 ester group; or
An amino group, an azine group, an azo group, an ureido group, an isocyanate group, an oxyimino group, a morpholinyl group, a piperazinyl group, a fluoro group, a chloro group, a bromo group, an iodo group, a hydroxy group, A C3 to C10 cycloalkyl group which is unsubstituted or substituted with at least one functional group selected from a C1 to C10 alkoxy group, a C1 to C10 ketone group, a C1 to C10 amine group, and a C1 to C10 ester group,
X 4 to X 6 are each independently substituted or unsubstituted with at least one functional group selected from the group consisting of a vinyl group, an acryl group, a methacryl group, a thiol group, a mercapto group, a C1 to C10 sulfur group, and a C6 to C20 aryl group; An unsubstituted C1 to C30 alkyl group;
A C1 to C30 alkenyl group substituted or unsubstituted with at least one functional group selected from a vinyl group, an acryl group, a methacryl group, a thiol group, a mercapto group, a C1 to C10 sulfur group, and a C6 to C20 aryl group;
A C1 to C30 alkynyl group substituted or unsubstituted with at least one functional group selected from a vinyl group, an acrylic group, a methacrylic group, a thiol group, a mercapto group, a C1 to C10 sulfur group, and a C6 to C20 aryl group; or
Is a C3 to C10 cycloalkyl group substituted or unsubstituted with at least one functional group selected from a vinyl group, an acryl group, a methacryl group, a thiol group, a mercapto group, a C1 to C10 sulfur group, and a C6 to C20 aryl group.
The M may be Si, Ti, or a combination thereof.
The graphene-containing ceramic hybrid sol solution may further comprise a first additive selected from inorganic powders, organic additives, or combinations thereof.
The organic additive may be included in an amount of 0.01 to 10 parts by weight based on 100 parts by weight of the graphene-containing ceramic hybrid sol solution.
The organic additive may be selected from the group consisting of a curing agent, a resin binder, a monomer, a dispersant, a dispersion stabilizer, a surfactant, a polyimide precursor, an organic solvent, an amphoteric solvent, a hydrophilic solvent, A coupling agent, a thermoplastic resin, a conductive polymer, or a combination thereof.
Another embodiment of the present invention includes a first ceramic hybrid coating film and a second ceramic hybrid coating film disposed on at least one side of the first ceramic hybrid coating film,
Wherein the second ceramic hybrid coating film comprises graphene, a resin binder, an organic solvent, and an organosilane compound,
The content of graphene in the first ceramic hybrid coating film is different from the content of graphene in the second ceramic hybrid coating film.
The content of graphene in the second ceramic hybrid coating film may be 0.001 wt% to 10 wt% based on the total weight of the second ceramic hybrid coating film.
The second ceramic hybrid coating may be selected from organic additives, nanoparticles, ceramics, dispersants, nanowires, carbon nanotubes, quantum dots, metals, salts, semiconductors, semiconducting materials, binders, monomers, silanes, polymers, And may further comprise a second additive.
The second additive may be included in an amount of 0.01 to 10 parts by weight based on 100 parts by weight of the second ceramic hybrid coating layer.
Wherein the nanoparticles are selected from the group consisting of SiO 2 ; Dispersed silica sol; Dispersed silica solution; A surface-modulated SiO 2 and an oxide of Al 2 O 3 , Li 4 Ti 5 O 12 , TiO 2 , SnO 2 , CeO 2 , ZrO 2 , V 2 O 5 , B 2 O 3 , BaTiO 3 , Y 2 O 3 , WO 3, MgO, CuO, ZnO, AlPO 4, AlF, Si 3 N 4, AlN, TiN, WC, SiC, TiC, MoSi 2, Fe 2 O 3, GeO 2, Li 2 O, MnO, NiO, zeolites, hollow Ceramics, and mixed dispersion sols of these; A surface-modulated SiO 2 and an oxide of Al 2 O 3 , Li 4 Ti 5 O 12 , TiO 2 , SnO 2 , CeO 2 , ZrO 2 , V 2 O 5 , B 2 O 3 , BaTiO 3 , Y 2 O 3 , WO 3, MgO, CuO, ZnO, AlPO 4, AlF, Si 3 N 4, AlN, TiN, WC, SiC, TiC, MoSi 2, Fe 2 O 3, GeO 2, Li 2 O, MnO, NiO, zeolites, hollow Ceramic, ceramics, and mixed dispersions thereof, and combinations thereof.
In another embodiment of the present invention, there is provided a graphene dispersion comprising graphene dispersed, 0.001 to 15 wt% of the graphene dispersed, at least one precursor of the hydrophilic hydrate represented by the formula (1) 0.001 wt% to 10 wt% of at least one precursor of the hydrophobic hydrate represented by the following formula (1), 0.02 wt% to 20 wt% of silica nanoparticles, and a hydrophilic solvent, and hydrolysis and polycondensation reaction of the mixture, Containing ceramic sol solution, applying the ceramic hybrid sol solution to a substrate, drying the ceramic hybrid sol solution at a temperature of 25 ° C to 400 ° C, and heat treating the dried film at a temperature of 50 ° C to 900 ° C to form a coating film A method for producing a ceramic hybrid functional coating film,
Wherein the ceramic hybrid coating film has a water droplet contact angle of 20 DEG or less, or 60 DEG or more.
A ceramic hybrid coating film for mixing the dispersed graphene oxide (RGO) in an amount of 0.001 wt% to 10 wt% and mixing the precursor of the hydrophilic hydrate represented by the formula (1) in an amount of 0.001 wt% to 10 wt% As a manufacturing method, the water droplet contact angle of the ceramic hybrid coating film may be 12 DEG or less.
A process for producing a ceramic hybrid coating film in which 0.001 to 10% by weight of the reduced graphene oxide (RGO) is mixed and 0.001 to 10% by weight of a precursor of the hydrophobic hydrate represented by the formula (2) As a result,
The water droplet contact angle of the ceramic hybrid coating may be 90 DEG or more.
The dispersion treatment of the graphene can be carried out by a mechanical dispersion treatment or a solvent substitution method.
The solvent substitution method comprises the steps of: preparing a dispersion comprising a graphene powder, a first dispersant, and a first non-aqueous solvent to form a dispersion comprising a graphene-first dispersant and a first non-aqueous solvent; Adding a precursor of a second non-aqueous solvent and a hydrate to the dispersion to prepare a mixture; And mixing the mixture with a second dispersant and water to prepare a coating composition for forming graphene-containing organic-inorganic ceramic hybrid sol.
Another embodiment of the present invention is characterized in that the method further comprises the step of applying a second ceramic hybrid coating film on at least one side of the first ceramic hybrid coating film, wherein the content of graphene in the first ceramic hybrid coating film The present invention provides a method for producing a ceramic hybrid multilayer coating film which is different from the content of graphene in a ceramic hybrid coating film.
The content of graphene in the second ceramic hybrid coating film may be 0.001 wt% to 10 wt% based on the total weight of the second ceramic hybrid coating film.
Another embodiment of the present invention provides a car head lamp comprising a ceramic hybrid coating film or a ceramic hybrid multilayer coating film.
The present invention relates to a ceramic hybrid coating film having hydrophilicity or water repellency and improved thermal stability and transparency, a ceramic hybrid multilayer coating film containing the ceramic hybrid coating film and improved thermal conductivity, and a method of manufacturing the same, This makes it possible to realize an excellent automotive head lamp for preventing fogging.
1 is a schematic diagram showing an example of a ceramic hybrid multilayer coating film to be implemented in the present invention.
2 is a schematic view showing various forms of hydrates included in the coating composition for forming ceramic hybrid sol according to an embodiment of the present invention.
FIG. 3 is a schematic diagram showing a condensate of a hydrate precursor in a ceramic hybrid coating film according to an embodiment of the present invention. FIG.
4 is a photograph showing the dispersion stability and the storage stability of the coating composition for forming ceramic hybrid sol according to an embodiment of the present invention.
5 is a photograph showing uniformity and transparency of a ceramic hybrid coating film according to an embodiment of the present invention.
6 is a graph illustrating a measurement result of a contact angle of a water droplet of a ceramic hybrid coating film according to an embodiment of the present invention.
7 is a graph showing the thermal conductivity effect of the ceramic hybrid coating film according to an embodiment of the present invention.
FIG. 8 is a schematic view showing a water droplet contact angle of a ceramic hybrid coating film according to an embodiment of the present invention. FIG.
Hereinafter, embodiments of the present invention will be described in detail. However, it should be understood that the present invention is not limited thereto, and the present invention is only defined by the scope of the following claims.
The ceramic hybrid coating film according to an embodiment may include 0.0005 to 15% by weight of graphene oxide (RGO); 0.001 wt% to 10 wt% of at least one hydrophilic hydrate represented by the formula (1) or at least one hydrophobic hydrate represented by the formula (2); 0.02% to 20% by weight of silica nanoparticles; And a hydrophilic solvent balance,
The water droplet contact angle of the ceramic hybrid coating film is 20 DEG or less, or 60 DEG or more.
The dispersed graphene may be contained in an amount of 0.0005 to 15% by weight based on the total amount of the graphene-containing ceramic hybrid sol solution.
By including highly dispersed graphene in the ceramic hybrid sol solution, thermal conductivity and surface functionality can be improved.
For example, when the dispersed graphene is applied to a hydrophilic hydrate, the water droplet contact angle of the ceramic hybrid coating film may be less than 20 ° and thus exhibit hydrophilic properties.
When the graphene dispersion is applied to the hydrophobic hydrate, the water droplet contact angle of the ceramic hybrid coating film becomes 60 ° or more, and water repellency can be exhibited.
When the content of the graphene dispersed is increased to 0.001 wt% to 10 wt% and applied to the hydrate of the hydrophilic silane compound, the water droplet contact angle of the ceramic hybrid coating film becomes 12 ° or less, And when the content of the graphene dispersed is increased from 0.001 wt% to 10 wt% to the hydrate of the hydrophobic silane compound, the water droplet contact angle of the ceramic hybrid coating film becomes 90 DEG or more, The water repellency characteristics close to the characteristics can be expressed.
The graphene of the present invention means a plate-like material in which the thickness of the BASAL plane is in the order of atom / molecule to nano unit, and the planar base plane is graphene oxide (graphite oxide), reduced graphene oxide (rGO) Means a graphene nanoplate (in which expanded graphite is peeled off), and further means a graphene oxide modified form (a substituent is modified, a derivative, a combination with a third material, etc.), or a doped form.
The graphene of the present invention can be produced by preparing graphene oxide (GO, commonly referred to as graphite oxide), irradiating graphene oxide with energy (microwave, photon, IR, laser, etc.) . ≪ / RTI > At this time, the reduction method is largely divided into a thermal reduction method and a chemical reduction method.
The graphene may also be produced by immersing graphene in a solvent having excellent affinity with graphite, and then treating ultrasonic waves or the like to further remove the graphite. Representative examples of solvents having excellent affinity with graphite include GBL and NMP. The quality of graphene produced by this method is good, but it is difficult to mass-produce it.
Examples of the method include a chemical synthesis method, a bottom generation method, and a method of chemically cleaving carbon nanotubes. Examples of the method include a solvent removal method of graphite, a mechanical grinding method of graphite (ultrasonic wave, milling, An electrical peeling method, and a synthetic method.
On the other hand, oxidizing groups on the graphene surface can not be completely removed by any of the methods disclosed so far, and the oxygen content by the graphene surface oxidizing unit is usually 5 wt% or less with respect to the carbon backbone, except for GO . In the present invention, the term "graphene" is defined as a range of oxygen content by the surface oxidizing agent of 5 wt% or less based on the carbon backbone.
In the present invention, all of the above-mentioned forms are to be named as graphenes.
In the present invention, highly dispersed graphenes are used, and a method of highly dispersing graphenes will be described later in connection with a manufacturing method.
The hydrophilic hydrate of Formula 1 and the hydrophobic hydrate of Formula 2 may be expressed as follows.
[Chemical Formula 1]
X a n -M- (OH) 4-n
(2)
X b n -M- (OH) 4-n
In the above Formulas 1 and 2,
M is selected from Si, Ti, Ag, Sn, In, Zn, and combinations thereof,
X a represents an epoxy group, a glycidoxy group, a carboxyl group, an amino group, an azo group, an azo group, an ureido group, an isocyanate group, an oxyimino group, a morpholinyl group, a piperazinyl group, a fluoro group, a chloro group, , A C1 to C30 alkyl group substituted or unsubstituted with at least one functional group selected from a hydroxyl group, a C1 to C10 alkoxy group, a C1 to C10 ketone group, a C1 to C10 amine group, and a C1 to C10 ester group;
An amino group, an azine group, an azo group, an ureido group, an isocyanate group, an oxyimino group, a morpholinyl group, a piperazinyl group, a fluoro group, a chloro group, a bromo group, an iodo group, a hydroxy group, A C1 to C30 alkenyl group substituted or unsubstituted with at least one functional group selected from a C1 to C10 alkoxy group, a C1 to C10 ketone group, a C1 to C10 amine group, and a C1 to C10 ester group;
An amino group, an azine group, an azo group, an ureido group, an isocyanate group, an oxyimino group, a morpholinyl group, a piperazinyl group, a fluoro group, a chloro group, a bromo group, an iodo group, a hydroxy group, A C1 to C30 alkynyl group substituted or unsubstituted with at least one functional group selected from a C1 to C10 alkoxy group, a C1 to C10 ketone group, a C1 to C10 amine group, and a C1 to C10 ester group; or
An amino group, an azine group, an azo group, an ureido group, an isocyanate group, an oxyimino group, a morpholinyl group, a piperazinyl group, a fluoro group, a chloro group, a bromo group, an iodo group, a hydroxy group, A C3 to C10 cycloalkyl group which is unsubstituted or substituted with at least one functional group selected from a C1 to C10 alkoxy group, a C1 to C10 ketone group, a C1 to C10 amine group, and a C1 to C10 ester group,
X b is a C1 to C30 alkyl group substituted or unsubstituted with at least one functional group selected from a vinyl group, an acryl group, a methacryl group, a thiol group, a mercapto group, a C1 to C10 sulfur group, and a C6 to C20 aryl group ;
A C1 to C30 alkenyl group substituted or unsubstituted with at least one functional group selected from a vinyl group, an acryl group, a methacryl group, a thiol group, a mercapto group, a C1 to C10 sulfur group, and a C6 to C20 aryl group;
A C1 to C30 alkynyl group substituted or unsubstituted with at least one functional group selected from a vinyl group, an acrylic group, a methacrylic group, a thiol group, a mercapto group, a C1 to C10 sulfur group, and a C6 to C20 aryl group; or
A C3 to C10 cycloalkyl group which is substituted or unsubstituted with at least one functional group selected from a vinyl group, an acryl group, a methacryl group, a thiol group, a mercapto group, a C1 to C10 sulfur group, and a C6 to C20 aryl group,
n is an integer of 1 to 3;
Each of these may be contained in an amount of 0.001 wt% to 10 wt% based on the total amount of the graphene-containing ceramic hybrid sol solution.
By using a compound containing at least one of the organic functional groups X a or X b , the hydrophilic hydrate or the hydrophobic hydrate can be stably bonded at the interface with the organic component-ceramic component derived from the graphene-organic functional group, It is stable even in the heat treatment process, and a buffering effect is obtained even in an excessive inflow of the inorganic additive and the organic additive, so that a stable film can be formed.
The hydrophilic hydrate or hydrophobic hydrate may be individual polymers for each, or may be a copolymer of hydrophilic and hydrophobic components.
The term "hydrophilic" refers to a monomer, oligomer or polymer that exhibits greater affinity for water than other monomers, oligomers, or polymers, or monomeric repeating units of an oligomer or polymer, or a repeating monomeric ≪ / RTI > Examples of hydrophilic silane components include amino silanes, ureido silanes, isocyante silanes, oximino silanes, and chloro silanes. Particularly preferred examples of particularly preferred hydrophilic silane components are 3-aminopropyltriethoxysilane, 3-aminopropyltriethoxysilane, bis [(3-triethoxysilyl) propyl] Amines such as Bis [(3-Triethoxysilyl) Propyl] Amine, 3-Aminopropyltrimethoxysilane, 3-Aminopropylmethyldiethoxysilane, 3- Aminopropylmethyldimethoxysilane (3-aminopropylmethyldimethoxysilane), aminoethylaminopropyltrimethoxysilane, aminoethylaminopropyltriethoxysilane, aminoethylaminopropylmethyldimethoxysilane, aminoethylaminopropylmethyldimethoxysilane, aminoethylaminopropylmethyldimethoxysilane, (Aminoethylaminomethyldiethoxysilane), aminoethylaminomethyltriethoxysilane diethylenetriaminopropyltrimethoxysilane, diethylenetriaminopropyltrimethoxysilane, diethylenetriaminopropyltrimethoxysilane, diethylenetriaminopropyltrimethoxysilane, diethylenetriaminopropyltrimethoxysilane, diethylenetriaminopropyltrimethoxysilane, diethylenetriaminopropyltrimethoxysilane, But are not limited to, diethylenetriaminopropylmethyldimethoxysilane, diethylenetriaminopropylmethyldiethoxysilane, diethylenetriaminomethylmethyldiethoxysilane, diethylaminomethyltriethoxysilane, diethylaminomethyldiethoxysilane, (Diethylaminomethylmethyldiethoxysilane), diethylaminomethyltrimethoxysilane, diethylaminopropyltrimethoxysilane, diethylaminomethyltrimethoxysilane, Diethylaminopropylmethyldimethoxysilane, diethylaminopropylmethyldiethoxysilane, N- (N-butyl) -3-aminopropyltrimethoxysilane, N- , (N-phenylamino) methyltrimethoxysilane, (N-phenylamino) Methyltriethoxysilane, (N-phenylamino) methylmethyldimethyl (N-phenylamino) methylmethyldimethoxysilane, (N-phenylamino) methylmethyldiethoxysilane, 3- (N-phenylamino) propyltrimethoxysilane (3- Phenylamino) propyltrimethoxysilane, 3- (N-phenylamino) propyltriethoxysilane, 3- (N-phenylamino) propylmethyldimethoxysilane (3- Propylmethyldimethoxysilane), 3- (N-phenylamino) propylmethyldiethoxysilane (3- (N-Phenylamino) Propylmethy (Piperazinylpropylmethyldimethoxysilane), Piperazinylpropylmethyldiethoxysilane, Piperazinylmethylmethyldiethoxysilane, Morpholinylpropyltrimethoxysilane, and Pyridazinylpropyltrimethoxysilane. The term " , Morpholinylpropyltriethoxysilane, morpholinylpropylmethyldimethoxysilane, morpholinylpropylmethyldiethoxysilane, morpholinylmethyltrimethoxysilane, morpholinylmethyltrimethoxysilane, morpholinylmethyltrimethoxysilane, morpholinylmethyltrimethoxysilane, morpholinylmethyltrimethoxysilane, morpholinylmethyltrimethoxysilane, But are not limited to, morpholinylmethylmethyldiethoxysilane, aminohexylaminomethyltrimethoxysilane, hexanediaminomethyltriethoxysilane, aminohexylaminomethyltriethoxysilane, But are not limited to, aminosilanes such as methoxy silane, aminosilane silane, aminosilane silane, aminosilane silane, aminosilane silane, aminosilane silane, aminosilane silane, aminosilane silane silane, silane silane silane, But are not limited to, cyclohexylaminopropylmethyldimethoxysilane, cyclohexylaminopropylmethyldiethoxysilane, 3-ureidopropyltrimethoxysilane, 3-ureidopropyltriethoxysilane, 3-isocyanate But are not limited to, 3-isocyanatepropyltrimethoxysilane, 3-isocyanatepropyltriethoxysilane, trimethoxysilane, triethoxysilane, methyldimethoxysilane, dimethoxysilane, Methyldiethoxysilane, Methyltrimethoxysilane, Methyltriethoxysilane, Methyltripropoxysilane, Methyltributoxysilane, Methyltriethoxysilane, Methyltriethoxysilane, Methyltriethoxysilane, Methyltriethoxysilane, Dimethyl tris-butylperoxy silane, dimethylethoxysilane, dimethyldimethoxysilane, dimethyldiethoxysilane, ethyltrimethoxysilane, ethyltrimethoxysilane, ethyltrimethoxysilane, Propyltrimethoxysilane, propyltriethoxysilane, isobutyltriethoxysilane, N-butyltrimethoxysilane, N (trimethylsilyloxy) silane, N-methyltriethoxysilane, Butyltriethoxysilane, 1-butyltrimethoxysilane, 1-butyltriethoxysilane, 1-butyltriethoxysilane, and it is preferable to use one or more selected from the group consisting of hexylsilane, hexylsilane, hexylsilane, hexylsilane, hexylsilane, hexylsilane, hexylsilane, hoxysilane, allyltriethoxysilane, dodecyltrimethoxysilane, dodecylmethyldimethoxysilane, octodecyltrimethoxysilane, ), Octodecylmethyldimethoxysilane, N-octyltrimethoxysilane, N-octyltriethoxysilane, octylmethyldiethoxysilane, cyclohexyltriethoxysilane, octyltrimethoxysilane, But are not limited to, cyclohexyltriethoxysilane, tetraacetoxysilane, ethyltriacetoxysilane, methyltriacetoxysilane, dimethyldiacetoxysilane, di-tert-butoxy-diacetate Di-Tertbutoxy-Diacetoxysilane, Phenyltris (Methylethylketoxime) Silane, (Methylisobutylketoxime) silane, trimethyl (methylethylketoxime) silane, dimethyldi (methylethylketoxime) silane, methyl (methylethylketoxime) silane, Methyltris (Methylisobutylketoxime) Silane, Methyltris (Acetoxime) Silane, Methyltris (Methylethylketoxime) Silane, Vinyl But are not limited to, tris (methylisobutylketoxime) silane, methylvinyldi (cyclohexanoneoxime) silane, methylvinyldi (methylethylketoxime) silane, Silane, vinyltris (Methylethylketoxime) silane, 3-glycidoxypropyltrimethoxysilane, 3-glycidoxypropyltriethoxysilane, 3-glycidoxypropyltrimethoxysilane, oxysilane, 3-glycidoxypropylmethyldiethoxysilane, 3-glycidoxypropylmethyldimethoxysilane, and the like.
The term "hydrophobic" refers to monomeric, oligomeric, and polymeric compounds that contain moieties, oligomers, or polymers that have less affinity for water than other components to which they bind. Examples of relatively hydrophobic classes of silane components include vinyl silanes, methacrylate silanes, sulfur silanes, mercapto silanes, epoxy silanes, phenyl (meth) acrylates, And phenyl silanes. Particularly preferred examples of hydrophobic silane components include? -Methacryloxypropyltrimethoxy silane, cyclohexyltrimethoxysilane, phenyltrimethoxysilane, phenyltriethoxysilane (? -Methacryloxypropyltrimethoxysilane, Vinyltriethoxysilane, vinyltriethoxysilane, vinyltris (2-methoxyethoxy) silane, vinyltrisisopropoxysilane (Vinyltriethoxysilane), vinyltriethoxysilane ), Vinyltris (tert-butylperoxy) silane, vinyldimethylethoxysilane, vinylmethyldimethoxysilane, vinylmethyldiethoxysilane, allyl Allyltrimethoxysilane, Allyltriethoxysilane, Vinyltriacetoxysilane, Vinyltriacetoxysilane, Vinyltriacetoxysilane, Examples of the solvent include vinyltrichlorosilane, vinyldimethylchlorosilane, vinylmethyldichlorosilane, vinyltris (Methylisobutylketoxime) silane, methylvinyldi (cyclohexanoneoxime) silane (Methylvinyldi (Cyclohexanoneoxime) Silane), Methylvinyldi (Methylethylketoxime) Silane, Vinyltris (Methylethylketoxime) Silane, 3-methacryloxypropyl tri Methacryloxypropyltrimethoxysilane, 3-methacryloxypropyltrimethoxysilane, methacryloxypropyltris (trimethylsiloxy) silane, 3-methacryloxypropyltriethoxysilane, 3-methacryloxypropyltrimethoxysilane, (3-methacryloxypropylmethyldimethoxysilane), 3-methacryloxypropylmethyldiethoxysilane (3-methacryloxypropylmethyldimethoxysilane) 3-mercaptopropyltriethoxysilane, 3-mercaptopropyltriethoxysilane, 3-mercaptopropyltrimethoxysilane, 3-mercaptopropyltrimethoxysilane, 3-mercaptopropyltrimethoxysilane, (3-mercaptopropylmethyldimethoxysilane), bis (triethoxysilylpropyl) tetrasulfide, bis (triethoxysilylpropyl) disulfide, bis (triethoxysilylpropyl) Bis (triethoxysilylpropyl) polysulfide, thiocyanto silane: 3-thiocyanatopropyltriethoxysilane, vinyltriacetoxysilane, dimethyl dimethoxy silane, (N, N-dimethylaminopropyl) trimethoxysilane, (N, N-dimethylacetyl) silane, dimethyldiethoxysilane, diphenyldimethoxysilane, diphenyldiethoxysilane, N, N - {(2-aminoethyl) (3-aminopropyl)} trimethoxysilane, and the like.
The organic functional group may be, for example, an epoxy group, a ketone group, a carboxyl group, a hydroxyl group, an amino group, an amine group (which may be a primary, secondary or tertiary amine), a thiol group, S, P, N, Si, etc. may be contained in the backbone of the alkyl group, alkenyl group and alkynyl group, and some of them may be organic or inorganic ≪ / RTI >
Moreover, not particularly limited to the molecular weight, oligomers, when a macromolecular or polymeric form X a or X b 2, the third sol to the internal self-function of a hydrated form which can lead to gel reaction (-OH), -Si (OH) 2 , and -Si (OH) 3 , which bind to the surrounding molecules to diffuse the sol-gel reaction.
The formula (1) is represented by any one of the following formulas (1-1) to (1-3)
The formula (2) may be represented by any one of the following formulas (2-1) to (2-3).
[Formula 1-1]
X 1 -M- (OH) 3
[Formula 1-2]
X 1 X 2 -M- (OH) 2
[Formula 1-3]
X 1 X 2 X 3 -M- (OH)
[Formula 2-1]
X 4 -M- (OH) 3
[Formula 2-2]
X 5 X 6 -M- (OH) 2
[Formula 2-3]
X 7 X 8 X 9 -M- (OH)
In the above Formulas 1-1 to 1-3 and 2-1 to 2-3, the definitions of X 1 to X 3 are the same as those of X a described above, and the definitions of X 4 to X 6 are the same as those of X b Just as definition.
M may be selected from Si, Ti, Ag, Sn, In, Zn, and combinations thereof. Specifically, M may be Si or Ti.
As a most specific example according to one embodiment of the present invention, M may be Si.
When M is Si, examples of silane compounds used or commercially available in the present invention include trimethoxysilane, triethoxysilane, methyltrimethoxysilane, methyltriethoxysilane, ethyltrimethoxysilane, Ethyl triethoxysilane, propyltrimethoxysilane, propyltriethoxysilane, isobutyltriethoxysilane, glycidoxypropyltriethoxysilane, cyclohexyltrimethoxysilane, phenyltrimethoxysilane, phenyltriethoxy Silane, vinyltrimethoxysilane, vinyltriethoxysilane, allyltrimethoxysilane allyltriethoxysilane, dimethyldimethoxysilane, dimethyldiethoxysilane, diphenyldimethoxysilane and diphenyldiethoxysilane, (N, N'- Dimethylaminopropyl) trimethoxysilane, (N, N-dimethylaminopropyl) triethoxysilane and N, (2-aminoethyl) (3-aminopropyl) trimethoxysilane. But is not limited to.
In addition, precursors having M-OR bonds (alkoxy bonds) with other metals M, or M-OOR bonds (ester bonds) are also possible.
The hydrate represented by the above formula (1) or (2) is, for example, as shown in FIG. 2, such as X 1 -Si- (OH) 3 , X 1 X 2 -Si- (OH) 2 , X 1 X 2 X 3 -Si- ). ≪ / RTI > The organic components X 1, X 2, and when the Hydrolysis precursor reagent containing X 3 X 1, X 2, and X 3 is a modified form (chemical change, complex, salt formation, and so on) is contained there graphene And the organic material reacts before the carbon of the graphene during firing to protect the graphene.
X 1 , X 2 , and X 3 may be the same or different.
In addition, the hydrate may be polymerized (network formation is performed) as shown in Fig. 3 when forming a ceramic hybrid coating film. This results in the formation of a -Si-O-Si- bond as a condensed form and, in some cases, addition of -Si- and -O-Si- bonds to the substituent portions of X 1 , X 2 and X 3 . Particularly, when the X moiety contains an organic functional group such as an epoxy group, it can be cured by using a curing agent.
For example, in the case of glycidoxypropyltriethoxysilane, curing can be performed using a curing agent such as ethylenediamine for an epoxy group which is an organic functional group contained in the X portion.
The silica nanoparticles may be included in an amount of 0.02 wt% to 20 wt% based on the total amount of the graphene-containing ceramic hybrid sol solution.
The average diameter of the silica nanoparticles may be from 5 nm to 30 nm, more specifically from 10 to 30 nm, and most particularly, 25 nm.
The silica nanoparticles used in the present invention may be, for example, 7 nm, 15 nm, or 15 nm.
When the average diameter of the silica nanoparticles is in the above range, it is advantageous to exhibit the interface bonding property and the function of the coating film, that is, hydrophilicity or water repellency.
The hydrophilic solvent is the most important mediator for stability and reactivity of the sol. In order to easily fuse the hydrophilic ceramic sol with graphene, a precondition for dispersing the graphene in a hydrophilic solvent should be established.
The reason why hydrophilicity is required is that in the case of the main reaction of the present invention, water is necessarily required in the sol-gel reaction, and it has to be well fused with H 2 O as the reaction product, and silanol (-Si -OH) must be fused well with the surrounding solvent, a hydrophilic solvent having a single or biphasic system is required.
If the precondition for dispersing graphene in a hydrophilic solvent is not met, it is difficult to expect a uniform fusion of hydrophilic sol and graphene.
Herein, "precondition for dispersing graphene in a hydrophilic solvent" is, for example, three cases.
First, a dispersion of water-based graphene dispersed in water can be mentioned.
The water-based graphene dispersion can be prepared by applying electricity to graphite in a liquid phase, and grains formed in this manner are dispersed in water by substituting the water-based substituents (-OH, -COOH) for the end organo functional groups. By simply mixing this aqueous graphene dispersion with an aqueous ceramic sol, a homogeneous graphene-ceramic hybrid sol solution can be formed. That is, the aqueous graphene dispersion can be directly applied to the mixing process without the addition of a dispersant or an additional process.
Secondly, graphene containing a plurality of hydrophilic groups on the surface, that is, a case where aqueous graphene dispersed in water is used, may be mentioned.
According to one embodiment of the present invention, since the content of graphene mixed in the ceramic sol solution is as small as 0.01% by weight to 0.1% by weight, graphene containing a large amount of surface hydrophilic groups is dispersed in a hydrophilic solvent such as water or alcohol , Even when used in the preparation of a ceramic sol solution, a uniform hybrid sol solution can be prepared.
At this time, a binder, an inorganic powder, an organic additive, etc., which are added together, may serve as an auxiliary agent to prevent aggregation of graphene.
Third, graphenes are dispersed in a non-aqueous solvent so that the graphenes can be highly dispersed, and then the solvent is replaced with an aqueous solvent. In the present invention, this is referred to as a solvent substitution method, and specific solvent substitution methods will be described later.
Specific examples of the hydrophilic solvent include water; But are not limited to, alcohols such as methanol, ethanol, propanol, butanol, and isopropyl alcohol (IPA), glycols, or combinations thereof. For example, a mixed solvent of water and alcohol.
The hydrophilic solvent may be mixed in an amount of 10 to 500 parts by weight based on 100 parts by weight of water, and specifically, the mixing ratio by weight of water to alcohols is 100: 50, 100: : 100, 100: 150, 100: 200, 100: 300, 100: 400. 100: 500, and may be mixed at a weight ratio of usually 100: 100, or 100: 200.
The graphene-containing ceramic hybrid sol solution may further comprise a first additive selected from inorganic powders, organic additives, or combinations thereof.
By further including the inorganic powder, the stability of the coating film (composite effect) and the film functionality such as super hydrophilicity can be imparted.
There may be mentioned ceramic particles as the preferred embodiment of the inorganic powder, as a specific example of the ceramic particles, SiO 2, Al 2 O 3, Li 4 Ti 5 O 12, TiO 2, SnO 2, CeO 2, ZrO 2, V 2 O 5, B 2 O 3,
Examples of the method for obtaining the graphene-ceramic composite powder by applying the ceramic grains to the graphene include a graphen-metal precursor reduction method, a graphen-ceramic precursor heat treatment method, a plating method, a substitution method, and a sputtering method.
The diameter of the inorganic powder may be 5 nm to 50 nm.
Specifically, it may be from 5 nm to 30 nm, more specifically from 7 nm to 25 nm, for example from 10 nm to 20 nm.
If the diameter is out of the above range, physical properties of the film may be deteriorated.
The inorganic powder may be included in an amount of 5 to 30 parts by weight based on 100 parts by weight of the graphene-containing ceramic hybrid sol solution.
Specifically, it may be 5 parts by weight to 25 parts by weight, more specifically 7 parts by weight to 20 parts by weight, for example, 7 parts by weight to 10 parts by weight.
If the content of the inorganic powder is out of the above range, physical properties of the coating may be deteriorated.
By further including the organic additive, dispersibility, coating property, stability, adhesiveness, leveling property, viscosity property, coating film property, dry property and the like can be improved.
The organic additive may be selected from the group consisting of a curing agent, a resin binder, a monomer, a dispersant, a dispersion stabilizer, a surfactant, a polyimide precursor, an organic solvent, an amphoteric solvent, a hydrophilic solvent, A silane coupling agent, a thermoplastic resin, a conductive polymer, or a combination thereof, but is not limited thereto.
The organic additive may be included in an amount of 0.01 to 10 parts by weight based on 100 parts by weight of the graphene-containing ceramic hybrid sol solution.
Specifically, it may be contained in an amount of 1 part by weight to 10 parts by weight, more specifically 3 parts by weight to 10 parts by weight.
Specific examples of the resin binder include thermosetting resin (urethane resin, epoxy resin, melamine resin, polyimide, and mixtures thereof), photocurable resin (epoxy resin, polyethylene oxide, urethane resin and mixture thereof, Acrylate, a polyester acrylate, a urethane acrylate, a polyether acrylate, a thiolate, an organosilicon polymer, an organosilicon copolymer and a mixture thereof, a reactive monomer is a monofunctional monomer such as 2-ethylhexyl acrylate Acrylate, methacrylic acid, methacrylic acid, methacrylic acid, methacrylic acid, methacrylic acid, methacrylic acid, methacrylic acid, maleic anhydride, Ethyl acrylate, hydroxyethyl methacrylate, Butyl acrylate, hydroxypropyl methacrylate, hydroxybutyl acrylate, and hydroxybutyl methacrylate, and the like. Examples of the reactive monomers include 1,3-butanediol diacrylate, 1,4-butanediol diacrylate , 1,6-hexanediol diacrylate, diethylene glycol diacrylate, diethylene glycol dimethacrylate, neopentyl glycol diacrylate, ethylene glycol dimethacrylate, tetraethylene glycol methacrylate, polyethylene glycol di Methacrylate, tripropylene glycol diacrylate, 1,6-hexanediol diacrylate, and mixtures thereof, a reactive monomer is a trifunctional monomer such as trimethylolpropane triacrylate, trimethylolpropane trimethacrylate, penta Erythritol triacrylate, glycidyl penta triacrylate, glycidyl There may be mentioned other triacrylate and mixtures thereof, a photoinitiator, benzophenone, benzyl dimethyl Kane talgye, acetophenone, anthraquinone, and the polymer, and so on) a mixture thereof,
Specific examples of the monomers include thermosetting monomers, UV-curable monomers, and chemically curable monomers.
Specific examples of the dispersant and the dispersion stabilizer include Triton X-100, polyethylene oxide, polyethylene oxide-polypropylene oxide copolymer, polyvinylpyrrole, polyvinyl alcohol, Ganax, starch, polysaccharide, dodecyl benzene sulfate, sodium dodecyl benzene sulfonate (NaDDBS), sodium dodecylsulfonate (SDS), 4-vinylbenzoic acid Such as cetyltrimethylammounium 4-vinylbenzoate, pyrene derivatives, Gum Arabic, GA, nafion and mixtures thereof, and other surfactants such as LDS (Lithium Dodecyl Sulfate), CTAC (Cetyltrimethyl Ammonium Chloride), DTAB (Dodecyl-trimethyl Ammonium Bromide), nonionic C12E5 (Pentaoxoethylenedocyl ether), polysaccharide (Dextrin), PEO (Poly Ethylene Oxide), Gum Arabic ene cellulose, commercial BYK, block copolymer, BTK-Chemie, Germany), leveling agent,
The silane coupling agent is a compound capable of forming Si (OH) 4 by hydrolysis and condensation reaction, and examples thereof include tetramethoxysilane, tetraethoxysilane, tetra-n-propoxysilane, Tetraalkoxysilanes composed of tetraisopropoxysilane, tetra-n-butoxysilane, tetra-sec-butoxysilane, tetra-tert-butoxysilane and mixtures thereof; Methyltrimethoxysilane, ethyltrimethoxysilane, ethyltriethoxysilane, n-propyltrimethoxysilane, n-propyltriethoxysilane, i-propyltrimethoxysilane, i- Propyltriethoxysilane, n-butyltrimethoxysilane, n-butyltriethoxysilane, n-pentyltrimethoxysilane, n-hexyltrimethoxysilane, n-heptyltrimethoxysilane, n- Vinyltrimethoxysilane, trimethoxysilane, trimethoxysilane, vinyltrimethoxysilane, vinyltriethoxysilane, cyclohexyltrimethoxysilane, cyclohexyltriethoxysilane, phenyltrimethoxysilane, phenyltriethoxysilane, 3-chloropropyltrimethoxysilane , 3-chloropropyltriethoxysilane, 3,3,3-trifluoropropyltrimethoxysilane, 3,3,3-trifluoropropyltriethoxysilane, 3-aminopropyltrimethoxysilane, 3 -Aminopropyltriethoxysilane, 2-hydroxyethyltrimethoxysilane, 2-hydroxyethyltriethoxysilane, 2-hydroxypropyltrimethoxysilane, 2-hydroxypropyltriethoxysilane, 3-hydroxypropyltrimethoxysilane, 3-hydroxypropyltriethoxysilane, 3-mercaptopropyltrimethoxysilane, 3-mercaptopropyltriethoxysilane, 3-mercaptopropyltriethoxysilane, 3-isocyanatopropyltrimethoxysilane, 3-isocyanatopropyltriethoxysilane, 3-glycidoxypropyltrimethoxysilane, 3- (Meth) acryloxypropyltrimethoxysilane, 3- (3,4-epoxycyclohexyl) ethyltrimethoxysilane, 2- (3,4-epoxycyclohexyl) Methacryloxypropyltriethoxysilane, 3-ureidopropyltrimethoxysilane, 3-ureidopropyltriethoxysilane, and mixtures thereof; Dimethyldimethoxysilane, diethyldimethoxysilane, diethyldiethoxysilane, di-n-propyldimethoxysilane, di-n-propyldiethoxysilane, di-i-propyldimethoxysilane, di di-n-butyldimethoxysilane, di-n-butyldiethoxysilane, di-n-pentyldimethoxysilane, di-n-pentyldiethoxysilane, di- N-hexyldiethoxysilane, di-n-heptyldimethoxysilane, di-n-heptyldiethoxysilane, di-n-octyldimethoxysilane, di- n-cyclohexyldimethoxysilane, di-n-cyclohexyldiethoxysilane, diphenyldimethoxysilane, diphenyldiethoxysilane and dialkoxysilanes composed of a mixture thereof, and mixtures thereof . They can also act as dispersion stabilizers.
The thermoplastic resin may be selected from the group consisting of polystyrene and its derivatives, polystyrene butadiene copolymer, polycarbonate, polyvinyl chloride, polysulfone, polyethersulfone, polyetherimide, polyacrylate, polyester, polyimide, polyamic acid, cellulose acetate, , Polyolefin, polymethyl methacrylate, polyether ketone, polyoxyethylene, and mixtures thereof,
The conductive polymer may be selected from a polythiophene-based homopolymer, a polythiophene-based copolymer, polyacetylene, polyaniline, polypyrrole, poly (3,4-ethylenedioxythiophene), pentacene-based compounds, and mixtures thereof.
The organic additive may be included in an amount of 0.01 to 10 parts by weight based on 100 parts by weight of the coating composition for forming a ceramic-organic hybrid sol.
Specifically, it may be 0.01 to 5 parts by weight, more specifically 0.1 to 3 parts by weight, for example, 0.01 to 2 parts by weight.
If the content of the organic additive is out of the above range, the physical properties of the coating film may be deteriorated.
In addition to the above-mentioned inorganic powder and organic additives, if necessary, antioxidants, carbon nanotubes, metal nanowires (such as silver nanowires), metal flakes, nanoparticles, metal nanoparticles, fullerenes, semiconductor nanoparticles , Semiconductor nanowires, semiconductor nanowires, and quantum dots.
The curing agent is used for curing the curable resin, and the curing may be performed by reacting using a catalyst, or may be formed by crosslinking with a curing agent.
The curing agent is not particularly limited, and any compound that is commonly used as a curing agent for an ordinary epoxy resin can be used. Examples thereof include amine compounds, amide compounds, acid anhydride compounds, phenol compounds and the like. Specific examples of the amine compound include diaminodiphenylmethane, ethylenediamine, diethylenetriamine, triethylenetetramine, diaminodiphenylsulfone, isophoronediamine, imidazole, BF3-amine complexes and guanidine derivatives. Examples of the amide compound include dicyandiamide, a polyamide resin synthesized from dimer of linolenic acid and ethylenediamine, and examples of the acid anhydride compound include phthalic anhydride, trimellitic anhydride, pyromellitic anhydride, Examples of the phenol compound include phenol novolak resin, cresol novolak resin, cresol novolak resin, and the like. Examples of the phenol compound include phenol novolak resin, cresol novolak resin , Aromatic hydrocarbon formaldehyde resin-modified phenol resin, dicyclopentadiene phenol addition-type resin, phenol aralkyl resin Naphthol aralkyl resin, trimethylol methane resin, tetraphenylol ethane resin, naphthol novolac resin, naphthol novolak resin, naphthol novolak resin, naphthol novolak resin, naphthol novolak resin, Phenol-co-axial novolak resin, naphthol-cresol co-novolak resin, biphenyl-modified phenol resin (polyhydric phenol compound having a phenylene core linked to a bismethylene group), biphenyl-modified naphthol resin (bifunctional naphthol- Aminotriazine-modified phenol resins (polyhydric phenol compounds in which phenol nuclei are linked via melamine, benzoguanamine, etc.) or alkoxy group-containing aromatic ring-modified novolak resins (formaldehyde having phenolic core and alkoxy group- A polyhydric phenol compound). These curing agents may be used singly or in combination of two or more kinds.
The amount of the epoxy resin and the curing agent to be blended in the epoxy resin composition of the present invention is not particularly limited, but it is preferable that the active group in the curing agent is 0.7 to 1.5 equivalents relative to one equivalent of the total epoxy groups of the epoxy resin.
For example, in the case of glycidoxypropyltriethoxysilane, the epoxy group, which is a functional group contained in the X portion, can be cured using a curing agent such as ethylenediamine.
The ceramic hybrid multilayer coating film according to another embodiment includes a ceramic hybrid coating film (hereinafter referred to as "first ceramic hybrid coating film") and a second ceramic hybrid coating film disposed on at least one side of the first ceramic hybrid coating film Wherein the second ceramic hybrid coating film comprises graphene, a resin binder, an organic solvent, and an organosilane compound, which are dispersed, and the content of graphene and the content of the silane compound in the first ceramic hybrid coating film One of which differs from at least one of the content of graphene in the second ceramic hybrid coating film and the content of the silane compound.
According to an embodiment of the present invention, the ceramic hybrid multilayer coating film may be, for example, a structure in which a second ceramic hybrid coating film is disposed under the first ceramic hybrid coating film, but is not limited thereto.
Referring to FIG. 1, it can be seen that the stacked structure of the substrate-B layer-A layer and the substrate-A layer-B layer are stacked in this order.
The A layer may be a first ceramic hybrid coating film according to an embodiment of the present invention, and the B layer may be a second ceramic hybrid coating film.
The ceramic hybrid sol solution forming the layer A may further include additives selected from inorganic powders, organic additives, or a combination thereof, as described above, and may further include the above-mentioned other additives as required.
The ceramic hybrid sol solution forming the B layer may contain graphene, a resin binder, an organic solvent, and an organosilane compound that have been subjected to dispersion treatment.
The A layer and the B layer may be independently constituted by a plurality of grains having different graphene contents and the content of graphene dispersed in the A layer is different from the graphene content dispersed in the B layer can do.
The content of graphene that may be contained in the B layer may be, for example, 0.001 wt% to 10 wt%, more specifically 0.1 wt% to 10 wt%, more specifically, 1 wt% to 1 wt%, based on the total weight of the second ceramic hybrid sol solution. By weight to 5% by weight.
For example, it may be composed of a double layer film of AB, BA, or a multilayer film of ABAB, ABB ', BABA, BAB' or the like.
And B 'means another layer B having a different graphene content.
The graphene used in the B layer is selected from the group consisting of graphene oxide (GO), reduced graphene oxide (rGO), graphene nanoplate, doped graphene, doped graphene oxide, and surface modified graphene oxide At least one species.
The organic solvent is not limited as long as it can mix and disperse the dispersed graphene, resin binder, and organosilane compound.
Examples of the solvent include solvents that can be mixed with hydrophilic solvents such as toluene, higher alcohols, ester compounds, ethyl acetate, methyl acetate, and the like.
Specific details of the dispersed graphene and the resin binder contained in the second ceramic hybrid coating film are as described above.
The second ceramic hybrid coating may be selected from organic additives, nanoparticles, ceramics, dispersants, nanowires, carbon nanotubes, quantum dots, metals, salts, semiconductors, semiconducting materials, binders, monomers, silanes, polymers, And may further comprise a second additive.
Wherein the nanoparticles are selected from the group consisting of SiO 2 ; Dispersed silica sol; Dispersed silica solution; A surface-modulated SiO 2 and an oxide of Al 2 O 3 , Li 4 Ti 5 O 12 , TiO 2 , SnO 2 , CeO 2 , ZrO 2 , V 2 O 5 , B 2 O 3 , BaTiO 3 , Y 2 O 3 , WO 3, MgO, CuO, ZnO, AlPO 4, AlF, Si 3 N 4, AlN, TiN, WC, SiC, TiC, MoSi 2, Fe 2 O 3, GeO 2, Li 2 O, MnO, NiO, zeolites, hollow Ceramics, and mixed dispersion sols of these; A surface-modulated SiO 2 and an oxide of Al 2 O 3 , Li 4 Ti 5 O 12 , TiO 2 , SnO 2 , CeO 2 , ZrO 2 , V 2 O 5 , B 2 O 3 , BaTiO 3 , Y 2 O 3 , WO 3, MgO, CuO, ZnO, AlPO 4, AlF, Si 3 N 4, AlN, TiN, WC, SiC, TiC, MoSi 2, Fe 2 O 3, GeO 2, Li 2 O, MnO, NiO, zeolites, hollow Ceramic, ceramics, and mixed dispersions thereof, and combinations thereof.
When the second additive is included, hydrophilicity or water repellency can be more clearly expressed. In particular, since the -OH, -COOH, ester group, and ketone group are included as functional groups of the additive, have.
0.01 to 10 parts by weight based on 100 parts by weight of the second graphene-containing ceramic hybrid sol solution.
Specifically 1 part by weight to 10 parts by weight, more specifically 3 parts by weight to 10 parts by weight.
The first ceramic hybrid coating layer and the second ceramic hybrid coating layer may be formed by different kinds of additives added to each layer.
The content of graphene in the first ceramic hybrid coating film is 1 wt% to 50 wt% with respect to the total weight of the first ceramic hybrid coating film, and the content of graphene in the first ceramic hybrid coating film is 1 wt% May be higher than the content of graphene.
The substrate may be a substrate or a first ceramic hybrid coating film, and may be a heterogeneous second ceramic hybrid coating film having a different content of graphene.
The substrate is a support member for forming a coating film, and is a substrate made of inorganic material such as glass, quartz, or silicon substrate; (PET), polyethylene naphthalate (PEN), polycarbonate (PC), cycloolefin polymer (COP), polymethylmethacrylate (PMMA), polystyrene (PS), polyimide (PI), polyarylate Or the like can be used.
Further, the substrate in the present invention can be used regardless of the type and shape of the substrate such as a large-area substrate, a curved substrate, and the like.
Meanwhile, the content of graphene in the first ceramic hybrid coating film may be 1 wt% to 50 wt% with respect to the total weight of the first ceramic hybrid coating film.
Specifically 2% to 50% by weight, more specifically 2% to 20% by weight.
In the case where an additive such as a polymer is not contained in the graphene-containing ceramic hybrid sol solution, it may be 4 wt% to 20 wt%, more specifically 4 wt% to 15 wt%
When an additive such as a polymer is included, the content of graphene may increase from 1 wt% to 50 wt%, specifically from 2 wt% to 50 wt%.
The graphene contained in the graphene-containing ceramic hybrid coating film can improve the strength and thermal conductivity of the coating film. However, when graphene is contained above a certain level, the graphene- And it may cause a problem in the interface bonding property. Therefore, it is recognized that it is very difficult to manufacture a coating film having smooth surface and uniform shape.
Accordingly, in the present invention, a coating film having improved strength and thermal conductivity by incorporating graphene at a level that does not deteriorate the bonding property with ceramics is manufactured.
The graft-containing ceramic hybrid sol solution for preparing a coating film according to an embodiment of the present invention includes a silane hydrate containing at least one organic functional group, thereby increasing the content of graphene contained in the hybrid sol solution .
In the case of a coating film formed from a graphene-containing ceramic hybrid sol solution containing a silane hydrate containing no organic functional group, the content of graphene in the coating film, which can be contained in an even dispersion of graphene in the sol solution, And may be 0.001% by weight to 1.8% by weight based on the weight. At this time, if the silane hydrate contains at least one organic functional group, bonding property of the interface between the graphene and the ceramic is improved and dispersibility is improved. Therefore, graphene in the coating film, The content can be improved to 0.001 wt% to 15 wt% based on the total weight of the coating film.
Further, when the inorganic powder, the organic additive, or a combination thereof is further included, the dispersibility is further improved, so that the content of graphene in the coating film, which can be contained in a uniformly dispersed form in the sol solution, And can be improved to 0.001 wt% to 50 wt% with respect to the weight.
On the other hand, in order to increase the transparency of the coating film, the graphene content should be reduced. The graphene content in the coating film, which may be contained in the sol solution evenly dispersed in the sol solution, may be 3 wt% 5% by weight, so that it is also useful for the production of a transparent film having excellent thermal conductivity.
For example, when the transmittance of the coating film is 50% or more, the content of graphene in the coating film is 0.01 wt% to 5 wt% based on the total weight of the coating film,
When the transmittance of the coating film is 80% or more, the content of graphene in the coating film may be 0.01 wt% to 3 wt% with respect to the total weight of the coating film.
1 is a schematic diagram showing an example of a functional coating film to be implemented in the present invention.
According to still another embodiment of the present invention, there is provided a method for producing a ceramic hybrid coating film, comprising: graphening a graphene dispersion; coating the graphene with 0.001 wt% to 15 wt% of the graphene, and at least one precursor of the hydrophilic hydrate represented by the formula , Or 0.001% by weight to 10% by weight of at least one hydrophobic hydrate precursor represented by the formula (2), 0.02% by weight to 20% by weight of silica nano particles, and a hydrophilic solvent, And the ceramic hybrid sol solution is applied to a base material and then dried at a temperature of 25 to 400 DEG C. The dried film is heat-treated at a temperature of 50 to 900 DEG C to obtain a graft- And a water droplet contact angle of the ceramic hybrid coating film is 20 DEG or less, or 60 DEG or more.
When 0.001 to 10% by weight of the reduced graphene oxide (RGO) is mixed with 0.001 to 10% by weight of the precursor of the hydrophilic hydrate represented by the formula (1), the water-drop contact angle of the ceramic hybrid coating Can be 12 degrees or less.
When 0.001 to 10% by weight of the graphene oxide (RGO) is mixed with 0.001 to 10% by weight of the precursor of the hydrophobic hydrate represented by the formula (2), the droplet contact angle of the ceramic hybrid coating film Lt; RTI ID = 0.0 > 90.
For example, the precursor of the hydrate may be glycidoxypropyltrimethoxysilane and may be used in admixture with a silane coupling agent selected from tetramethoxysilane, tetraethoxysilane, diphenylethoxysilane, and combinations thereof .
The coating step may be performed by a conventional coating method, and specifically, a coating method such as dip coating, spin coating, spray coating, paint coating, bar coating Or may be carried out by a combination of these methods. More specifically, the coating may be performed by dip coating, spin coating, or spray coating ). ≪ / RTI >
The coating process according to one embodiment can be performed by spray coating without any restriction on the type and shape of the substrate such as a large area and a curved substrate. However, the present invention is not limited thereto.
The method of manufacturing a ceramic hybrid multilayer coating film according to another embodiment may further include the step of applying a second ceramic hybrid coating film on at least one side of the first ceramic hybrid coating film in addition to the steps described above.
Meanwhile, the grains dispersed in the first ceramic hybrid coating film and the second ceramic hybrid coating film may be prepared in a highly dispersed form.
The step of preparing the highly dispersed graphene may be performed by a mechanical dispersion process or a solvent substitution process, and commercially available water-dispersed graphene may be used as highly dispersed graphene without any additional process.
The mechanical dispersion treatment is a dispersion method performed on dried graphene powder. The dried graphene powder is obtained by heat treatment of graphene oxide (GO) or reduction of graphene oxide by a chemical reduction method, drying the obtained graphene Can be obtained by heat treatment. Such graphene powder is highly agglomerated and can be dispersed by physical, chemical and mechanical methods. Representative examples may be performed by ultrasonication, stirring, shear stress and shearing force, homogenizer, beads, or a combination thereof.
The solvent substitution method is a dispersion method applied to wet graphene. Graphene obtained by the same method as the hydrazine reduction method is wetted with water. Since this water strongly adsorbs to graphene, it can be removed through a strong heat treatment . However, since strong heat treatment causes serious problems such as aggregation of graphene, it is possible to use a method of removing moisture at room temperature and then dispersing it again in a solvent having a property similar to that of the solvent constituting the coating liquid.
The solvent substitution method can be carried out, for example, by the steps shown below.
That is, the solvent substitution method comprises mixing a graphene powder, a first dispersant, and a first non-aqueous solvent to prepare a dispersion liquid comprising a graphene-first dispersant and a first non-aqueous solvent; Adding a precursor of a second non-aqueous solvent and a hydrate to the dispersion to prepare a mixture; And mixing the mixture with a second dispersant and water to prepare a graphene-containing oil-in-inorganic ceramic hybrid sol solution.
The method may further include a mechanical dispersion treatment step after mixing the graphene powder, the first dispersant, and the first non-aqueous solvent, and may further include washing with the non-aqueous solvent before the mechanical dispersion treatment.
Washing with a nonaqueous solvent can further maximize suitability in the latter process. Particularly, when considering the latter process, it is preferable to wash with the same or similar solvent as the first non-aqueous solvent.
That is, the step of washing with the non-aqueous solvent is performed to completely remove the moisture (H 2 O) adsorbed on the graphene surface, and may be performed only in the simple washing step, or in parallel with the ultrasonic dispersion treatment, The washing step may be carried out afterwards. This process can be performed multiple times as needed.
By performing the step of washing with the non-aqueous solvent, the long-term stability of the sol solution may be greatly influenced by the degree of water removal on the surface of the graphene. Thus, it is possible to control the physical properties that may be exhibited by containing moisture depending on the method and / or degree of performing the washing step.
In the first step of the method for preparing a graphene-ceramic hybrid coating film according to an embodiment of the present invention, even if only a very small amount of water is added, moisture is added to the sol Removal of moisture in the initial stage is very important, as it is less stable. Even if a small amount of water adsorbed on the graphene shows a lethal interface-instability at the interface with the sol, the stability of the entire graphene-ceramic hybrid mixed sol can be extremely deteriorated.
The first dispersant and the second dispersant used in the solvent substitution method may be independently selected from the group consisting of polyethylene glycol (PEG), glycerol, hydrochloric acid (HCl), acetic acid, formic acid, citric acid, a binder, have.
The first non-aqueous solvent and the second non-aqueous solvent may each independently be an amphoteric solvent, a water-soluble solvent other than water, a non-aqueous solvent, a polar solvent, a non-polar solvent, or a combination thereof.
Specifically, the first non-aqueous solvent and the second non-aqueous solvent are each independently selected from the group consisting of iso-propyl alcohol, ethanol, acetone, methyl ethyl ketone, methyl alcohol, ethyl alcohol, isopropyl alcohol, , Butyl alcohol, ethylene glycol, polyethylene glycol, tetrahydrofuran, dimethylformamide, dimethylacetamide, N-methyl-2-pyrrolidone, hexane, cyclohexanone, toluene, chloroform, dichlorobenzene, dimethyl Benzene, trimethylbenzene, pyridine, methylnaphthalene, nitromethane, acrylonitrile, octadecylamine, aniline, dimethylsulfoxide, or combinations thereof.
Graphenes of uniform size can be obtained by performing a process of highly dispersing graphene, centrifuging to discard the supernatant, and centrifuging the precipitate again to obtain a precipitate at least twice.
The content of graphene in the first ceramic hybrid coating film is different from the content of graphene in the second ceramic hybrid coating film.
For example, the content of graphene in the second ceramic hybrid coating film may be 0.001 wt% to 5 wt% based on the total weight of the second ceramic hybrid coating film.
Another embodiment of the present invention provides an automotive headlamp including the above-described ceramic hybrid coating film.
In particular, due to the effect of the present invention as described above, for example, excellent thermal conductivity, it is expected that the anti-fogging function due to heat conduction by the lamp heat can be exerted.
As an application example of a specific industry, it can be applied to a lens (PC curved substrate) of an automobile headlamp in which the problem of fogging is improved.
Hereinafter, specific examples of the present invention will be described. However, the embodiments described below are only intended to illustrate or explain the present invention, and thus the present invention should not be limited thereto.
In addition, contents not described here can be inferred sufficiently technically if they are skilled in the art, and a description thereof will be omitted.
Production Example 1
(Production of graphene (graphite) oxide)
10 g of natural graphite and 7.5 g of sodium nitrate were added to the reactor, and 621 g of 96% sulfuric acid was added slowly while stirring. When the three substances are sufficiently mixed, 45 g of manganese peroxide is added. Manganese peroxide is explosive when it reacts with concentrated sulfuric acid and generates heat and gas. After adding manganese dioxide, the mixture is stirred at room temperature and allowed to react for about 4 to 6 days. Then, 1L of 5% sulfuric acid is added, so heat and gas are generated. Cool the reactor appropriately and slowly add over 1 hour, and stir at room temperature for one day. After one day, 30 g of 30% hydrogen peroxide is slowly added and reacted for 2 hours. Several washing and centrifugation steps were performed to remove excess sulfuric acid and hydrogen peroxide in the final product. In this final step, centrifuge first, discard the supernatant, add a mixture of 3% sulfuric acid and 0.5% hydrogen peroxide in a 1: 1 mixture to the remaining supernatant, shake thoroughly, and centrifuge to discard the supernatant. Add the mixed solution to the remaining precipitate and mix. After repeating this process 15 times, replacing the mixed solution with water and repeating it 5-6 times, finally a water-based graphene oxide (GO) slurry is obtained.
The GO slurry is usually obtained by acid treatment of graphite or may be obtained naturally during purification. Therefore, the GO slurry in the present invention is not limited to this and may be a plate-like graphene oxide or graphite oxide which is generally known. Typically, the water-based GO slurry has a solids content of 2 to 8% by weight based on the centrifuged slurry.
(Preparation of dispersed GO)
The graphene oxide powder (GO) was put into ethanol to ultrasonically disperse (ultrasonically ultrasonically) a tip, or discharged at a high pressure into a fine nozzle to impart a shearing stress. The dispersant used was BYK series.
Production Example 2
(Preparation of thermally reduced graphene)
The water-based graphene-oxide slurry of Preparation Example 1 was vacuum-dried at 100 ° C. for 24 hours and then heat-treated at 600 ° C. in an N 2 atmosphere for 30 minutes to produce reduced graphene oxide (RGO).
(Production of dispersed RGO)
The dispersion was prepared by subjecting the graphene powder (RGO) to ethanol ultrasonic dispersion (Tip type ultrasonic treatment) or discharging fine nozzles at a high pressure (applying shear stress). The dispersant used was BYK series.
Production Example 3
(Preparation of chemically reduced graphene)
Hydrazine was added to the water-based graphene-oxide slurry of Preparation Example 1 to react for 24 hours, and the precipitate was centrifuged / washed / dried to produce reduced oxidized graphene powder.
(Production of dispersed RGO)
The dispersion was prepared by subjecting the graphene powder (RGO) to ethanol ultrasonic dispersion (Tip type ultrasonic treatment) or discharging fine nozzles at a high pressure (applying shear stress). The dispersant used was BYK series.
Production Example 4
(Preparation of Grain-Containing Ceramic Hybrid Sol Solution of Si (OH) 3 X 1 Type)
The graphene prepared in Preparation Example 3 15 mg was added to 100 ml of IPA and ultrasonic dispersion was performed for 10 minutes. After 1 hour, 1 ml of the top layer solution which did not settle out was collected, 100 ml of ethanol was added thereto, 10 ml of Glycidoxypropyl Trimethoxysilane (hereinafter referred to as GT) was added, ) Was changed in the range of 0.02 to 20% by weight for 24 hours. At this time, the pH was maintained at about 3.3. After the reaction, after the reaction, an ethylene diamine curing agent was added as much as GT mole, and after 30 minutes sintering, a graft-containing ceramic hybrid sol solution of Si (OH) 3 X 1 type was prepared. The results are shown in Table 1.
(Preparation of Coating Film - Single Membrane)
Examples 1 to 7
(Preparation of Graphene-Containing Ceramic Hybrid Coating Film I)
The graft-containing ceramic hybrid sol solution of the Si (OH) 3 X 1 type was spin-coated on a plasma-treated glass substrate (rpm 800). The spin-coated film was vacuum-dried at room temperature and then heat-treated at 180 ° C for 1 hour by a heat treatment method using a heater to prepare a graft-containing ceramic hybrid coating film.
The coating film forming process may be spray coating, bar coating, knife coating, screen printing, dip coating, or the like.
(Preparation of graphene-ceramic hybrid coating film II)
The graphene-ceramic hybrid sol solution of the Si (OH) 3 X 1 type was spray coated onto a plasma-treated PC (Polycarbonate) substrate. The spray coating film was vacuum dried at 50 ° C., And the surface heat treatment was performed. The heat treatment temperature was 300 占 폚, and the film exposure time was 3 seconds. The heat treatment and film exposure process were repeated. The temperature of the backside of the substrate was maintained at 80 ° C. to 130 ° C. during the heat treatment. This process was shown to be a favorable process for the plastic substrate, and the temperature To cool down the bottom of the substrate can be cooled (air-cooling is also possible).
Depends on silica content
Examples 1 to 7 and Comparative Examples 1 to 4 show that the graphene-containing ceramic hybrid coating film of the Si (OH) 3 X 1 type having a silica content of 0.02 to 20 wt% has a graphene content of 0.0005 to 70 wt% (Having a hydrate content of 0.0001 to 10% by weight and a hydrophilic solvent content in the composition).
Referring to Table 1, the maximum content of graphene in relation to the thermal conductivity and stability of the membrane is 15 wt%, and the hydrophilic properties (water drop contact angle of 20 DEG or less) are shown in Examples 1 to 7 .
Furthermore, it can be confirmed that the thermal conductivity is improved to some extent and the superhydrophilic property (water contact angle of 12 DEG or less) appears in the regions of Examples 2 to 4.
Example 8
(Si (OH) 3 X One + Si (OH) 2 X One X 2 Type graphene-containing ceramic hybrid coating film)
50 mg of the graphene prepared in Production Example 3 was placed in 100 ml of IPA and subjected to ultrasonic dispersion for 10 minutes. After 1 hour, 1 ml of the uppermost layer liquid which did not settle was collected. 100 ml of ethanol was added thereto, and then glycidoxypropyl trimethoxysilane (GT) and diphenyldiethoxysilane (weight ratio of 1: 1) Was dissolved in a mixed solvent of water: ethanol = 1: 1 by weight and added with nitric acid to adjust the pH to 2 to 4 and the mixture was stirred for 24 hours. Si (OH) 3 X 1 + Si (OH) 2 X 1 (molar ratio) was added to the reaction mixture in an amount of 0.02 to 20% by weight of rudox (15 nm silica sol) X 2 type graphene-ceramic hybrid sol solution was prepared and coated on a substrate to prepare a graphene-containing ceramic hybrid coating film.
It was confirmed that the transmittance was improved by about 15% and the strength of the film was improved from
Example 9
(Preparation of Grain-Containing Ceramic Hybrid Coating Film of Si (OH) 3 X 1 + Si (OH) 4 Type and Curing Agent Type)
Manufacturing example Grain made from 3 50 mg was added to 100 ml of IPA and ultrasonic dispersion was performed for 10 minutes. 1 ml of the top layer solution which did not settle after one hour was collected, 100 ml of ethanol was added thereto, and 10 to 10 ml of a mixture of glycidoxypropyl trimethoxysilane (hereinafter referred to as GT) and TMOS (weight ratio of 1: 40% by weight was dissolved in a mixed solvent of water: ethanol = 1: 1 by weight and added with nitric acid to adjust the pH to 2 to 4, and the reaction was carried out for 24 hours. The reaction product Ludox followed by the addition of 0.02 to 20 wt% of (a 15nm silica sol), were added as number of moles of ethylene diamine curing agent GT by
The content of graphene contained in the graphene-containing ceramic hybrid coating film was at most 4.5 to 5 wt%.
It was confirmed that the transmittance was improved by about 11% and the film strength was improved from pencil strength 4 to 5 as compared with the case of using Si (OH) 3 X 1 alone. The superhydrophilic property and the thermal conductivity property were maintained.
(Polymer added)
Example 10
The same procedure as in Example 8 was carried out except that 10 parts by weight of PVA was added to 100 parts by weight of the precursor of the graphene-solvent-hydrate before addition of the curing agent in the preparation of the graphene-containing ceramic hybrid sol solution according to Example 8 , A graphene-containing ceramic hybrid sol solution and a coating film formed therefrom were prepared.
It was confirmed that the content of the PVA was increased to 2, 5, and 10 times the weight of the silica nanoparticles, and the content of graphene contained in the coating film was improved to about 30 wt%, 50 wt%, and 60 wt% .
This is the result of confirming that the dispersion stability of graphene increases with the increase of organic component at the interface of ceramic-graphene.
Example 11
In the preparation of the graft-containing ceramic hybrid sol solution of the Si (OH) 3 X 1 type according to Production Example 4, 30% by weight of an aqueous solution of Rudox (LUDOX, silica nanoparticles of about 20 nm) as the source of silica nanoparticles by Aldrich, 30 wt% of water, 30 wt% of water and 30 wt% of GT were adjusted to pH 3.0, and mixed and stirred to prepare a ceramic hybrid sol solution further containing silica nanoparticles and a coating film formed therefrom. Was prepared in the same manner as in Example 1.
6 is a graph illustrating a measurement result of a contact angle of a water droplet of a ceramic hybrid coating film according to an embodiment of the present invention.
Specifically, FIG. 6 is a result of measuring the contact angle of water droplets on each coating film when a coating film is formed using the coating solution according to Example 1. FIG.
Referring to FIG. 6, the water droplet contact angle with respect to the coating film according to an embodiment of the present invention is 12.5 °, which shows a surface favorable to hydrophilic properties.
Example 12
Before adding the curing agent in the preparation of the graphene-containing ceramic hybrid sol solution according to Example 8, 0.1 part by weight of silver nanowire and 0.1 part by weight of silver nanoparticles were added to 100 parts by weight of the precursor of graphene-solvent-hydrate in place of 10 parts by weight of PVA , A graphene-containing ceramic hybrid sol solution and a coating film formed therefrom were prepared in the same manner as in Example 8.
Evaluation of uniformity (stability) of graphene-containing ceramic hybrid sol solution
FIG. 4 is a graph showing the effect of the graphene-containing ceramic hybrid sol solution prepared in Example 1 and Comparative Example 1 on the sol solution prepared in Example 1 and Comparative Example 1 in that graphene was added so that the content of uniformly dispersed graphene in the coating film formed from the resulting graphene- This is a result. 4 shows that the dispersion stability is very excellent as a result of using Si (OH) 3 X 1 , and the right side of FIG. 4 shows that most of the precipitation occurred as a result of using only Si (OH) 4 have. In the right photograph of FIG. 4, the transparent brown portion of the supernatant means that the graphene amount is saturated, and the graphene content of the coating film obtained from the supernatant is 0.001 to 2% by weight.
In Examples 1 to 10, the same phenomenon as in the left photograph of FIG. 4 can be observed. The dispersion prepared according to the principle of the present invention exhibited a stability of about 1 month or more at a very high concentration (stability was maintained for 1 month or more even in a refrigerator and a 60 ° C thermal shock test) and exhibited improved stability not found in conventional graphene dispersions.
Evaluation of Stability of Graphene-Containing Ceramic Hybrid Coating Film
FIG. 5 shows the results of coating the coating solution obtained in Comparative Example 1 and Example 1 on a PC substrate and then drying it.
It can be seen that the film obtained in Comparative Example 1 was easily peeled off as it was wrinkled, and that the coating film of the present invention obtained in Example 1 exhibited a smooth and transparent surface, showing good coating properties.
Evaluation of Thermal Conductivity of Graphene-Containing Ceramic Hybrid Coating Films
The thermal conductivity of the graphene-containing ceramic hybrid coating film manufactured using the principle of the present invention was compared and evaluated using a home made thermal conductivity meter.
A device for evaluating the thermal conductivity of a graphene-containing ceramic hybrid coating film was prepared by heating a PC (poly carbonate) substrate (
The results of measuring the thermal conductivity using this apparatus are shown in Fig.
7 is a graph showing the thermal conductivity effect of the graphene-containing ceramic hybrid coating film according to an embodiment of the present invention.
In the case of using pure GT (ceramic sol) on a general PC substrate, the thermal conductivity had a temperature increase effect only by about 2.8 ° C. per hour, whereas in the case of the coating film according to Example 12, It has a temperature increasing effect and shows a large heat conduction effect. This shows that the graphenes are uniformly and well dispersed in the coating film according to the present invention, so that the physical properties of graphene are well expressed. If the graphene dispersion is unstable and interface delamination occurs, the thermal conductivity value can not be achieved, for example, when the ceramic sol contains only the ceramic sol at around 2.8 DEG C and below.
In the present invention, it can be seen that the improvement in thermal conductivity at a minimum graphene content of 0.001 wt% is about twice that before graphene addition.
In the case of the coating film according to Example 12, the thermal conductivity was as high as 12.5 ° C as shown in FIG.
Examples 13 to 15 and Comparative Example 5
(Example 13), 7% by weight (Example 14) and 15% by weight (Example 15) of graphene were added to the composition of the water-repellent product Modesta BC-05 (Comparative Example 5) And the data of the contact angle of the water droplet with respect to the coating film is shown in FIG. 8 as a schematic diagram.
FIG. 8 is a schematic view showing a water droplet contact angle of a ceramic hybrid coating film according to an embodiment of the present invention. FIG.
8, the water repellency before the graphene addition (Comparative Example 5) showed a contact angle of about 60 °, but the graphene content was 0.005% by weight (Example 13), 7% by weight (Example 14) , 15% by weight (Example 15), the contact angle of the water droplet gradually increases and becomes close to the super water repellent contact angle (65 ° → 95 ° → 110 °).
This shows that the addition of graphene increases the super water repellency as well as the principle of increasing super hydrophilic properties.
(Preparation of coating film - double membrane)
A commercially available hydrophilic or water-repellent ceramic coating solution (nanotol product) was coated on the lower part of the first coating layer and dried to form a second ceramic hybrid coating layer using the ceramic hybrid coating layer according to any one of Examples 1 to 7 as a first coating layer, To form a coating film.
The results of measuring the thermal conductivity and the contact angle of the water droplet of the second ceramic hybrid coating film having the same thickness are shown in Table 2 below.
(Upper layer film)
(Water contact angle °)
Water Drop Contact Angle (°)
Table 2 shows the results of measurement of the thermal conductivity and the contact angle of the water droplets of the upper layer film with respect to the double membrane formed with the ceramic hybrid coating film of Table 1 as the upper layer film and the second ceramic hybrid coating film as the lower layer. The second ceramic hybrid coating film is configured such that the graphene content, or the composition of the coating film, is different from that of the first ceramic hybrid coating film.
Referring to Table 2, as the graphene content of the first ceramic hybrid coating film increases regardless of the composition of the second ceramic hybrid coating film and the contact angle of the water droplet, the thermal conductivity increases as well as the water droplet contact angle of the first ceramic hybrid coating film It can be seen that it is kept unaffected by.
Therefore, even when the composition of the second ceramic hybrid coating film, the contact angle of the water droplet, the graphene content, and the composition of the additive are different, it is possible to realize a desired water droplet contact angle in the first ceramic hybrid coating film and to exhibit excellent physical properties .
Particularly, when the first ceramic hybrid coating film and the second ceramic hybrid coating film have different graphene contents, more excellent effects are obtained in terms of thermal conductivity.
The above results can be similarly applied to the case where the third ceramic hybrid coating film is formed under the second ceramic hybrid coating film. Accordingly, in order to realize a coating film having improved thermal conductivity as well as hydrophilic or water repellent characteristics, a multilayer coating film is more advantageous than a single film.
Claims (22)
0.001 wt% to 10 wt% of at least one hydrophilic hydrate represented by the following formula (1) or at least one hydrophobic hydrate represented by the following formula (2);
0.02% to 20% by weight of silica nanoparticles; And
Hydrophilic solvent balance
A ceramic hybrid coating film formed from a graphene-containing ceramic hybrid sol solution,
The ceramic hybrid coating film has a water droplet contact angle of 20 DEG or less, or 60 DEG or more.
[Chemical Formula 1]
X a n -M- (OH) 4-n
(2)
X b n -M- (OH) 4-n
In the above Formulas 1 and 2,
M is selected from Si, Ti, Ag, Sn, In, Zn, and combinations thereof,
X a represents an epoxy group, a glycidoxy group, a carboxyl group, an amino group, an azo group, an azo group, an ureido group, an isocyanate group, an oxyimino group, a morpholinyl group, a piperazinyl group, a fluoro group, a chloro group, , A C1 to C30 alkyl group substituted or unsubstituted with at least one functional group selected from a hydroxyl group, a C1 to C10 alkoxy group, a C1 to C10 ketone group, a C1 to C10 amine group, and a C1 to C10 ester group;
An amino group, an azine group, an azo group, an ureido group, an isocyanate group, an oxyimino group, a morpholinyl group, a piperazinyl group, a fluoro group, a chloro group, a bromo group, an iodo group, a hydroxy group, A C1 to C30 alkenyl group substituted or unsubstituted with at least one functional group selected from a C1 to C10 alkoxy group, a C1 to C10 ketone group, a C1 to C10 amine group, and a C1 to C10 ester group;
An amino group, an azine group, an azo group, an ureido group, an isocyanate group, an oxyimino group, a morpholinyl group, a piperazinyl group, a fluoro group, a chloro group, a bromo group, an iodo group, a hydroxy group, A C1 to C30 alkynyl group substituted or unsubstituted with at least one functional group selected from a C1 to C10 alkoxy group, a C1 to C10 ketone group, a C1 to C10 amine group, and a C1 to C10 ester group; or
An amino group, an azine group, an azo group, an ureido group, an isocyanate group, an oxyimino group, a morpholinyl group, a piperazinyl group, a fluoro group, a chloro group, a bromo group, an iodo group, a hydroxy group, A C3 to C10 cycloalkyl group which is unsubstituted or substituted with at least one functional group selected from a C1 to C10 alkoxy group, a C1 to C10 ketone group, a C1 to C10 amine group, and a C1 to C10 ester group,
X b is a C1 to C30 alkyl group substituted or unsubstituted with at least one functional group selected from a vinyl group, an acryl group, a methacryl group, a thiol group, a mercapto group, a C1 to C10 sulfur group, and a C6 to C20 aryl group ;
A C1 to C30 alkenyl group substituted or unsubstituted with at least one functional group selected from a vinyl group, an acryl group, a methacryl group, a thiol group, a mercapto group, a C1 to C10 sulfur group, and a C6 to C20 aryl group;
A C1 to C30 alkynyl group substituted or unsubstituted with at least one functional group selected from a vinyl group, an acrylic group, a methacrylic group, a thiol group, a mercapto group, a C1 to C10 sulfur group, and a C6 to C20 aryl group; or
A C3 to C10 cycloalkyl group which is substituted or unsubstituted with at least one functional group selected from a vinyl group, an acryl group, a methacryl group, a thiol group, a mercapto group, a C1 to C10 sulfur group, and a C6 to C20 aryl group,
n is an integer of 1 to 3;
0.001 wt% to 10 wt% of the graphene oxide (RGO) and 0.001 wt% to 10 wt% of the hydrophilic hydrate represented by the formula (1), the ceramic hybrid coating film comprising:
Wherein the ceramic hybrid coating film has a water droplet contact angle of 12 DEG or less.
0.001 wt% to 10 wt% of the graphene oxide (RGO) and 0.001 wt% to 10 wt% of the hydrophobic hydrate represented by the formula (2), the ceramic hybrid coating film comprising:
Wherein the ceramic hybrid coating film has a water droplet contact angle of 90 DEG or more.
Wherein the average diameter of the silica nanoparticles is 5 nm to 30 nm.
The formula (1) is represented by any one of the following formulas (1-1) to (1-3)
(2) is a ceramic hybrid coating film represented by any one of the following formulas (2-1) to (2-3):
[Formula 1-1]
X 1 -M- (OH) 3
[Formula 1-2]
X 1 X 2 -M- (OH) 2
[Formula 1-3]
X 1 X 2 X 3 -M- (OH)
[Formula 2-1]
X 4 -M- (OH) 3
[Formula 2-2]
X 5 X 6 -M- (OH) 2
[Formula 2-3]
X 7 X 8 X 9 -M- (OH)
In Formulas 1-1 to 1-3, and 2-1 to 2-3,
M is selected from Si, Ti, Ag, Sn, In, Zn, and combinations thereof,
X 1 to X 3 each independently represent an epoxy group, a glycidoxy group, a carboxyl group, an amino group, an azo group, an azo group, an ureido group, an isocyanate group, an oxyimino group, a morpholinyl group, a piperazinyl group, Substituted with at least one functional group selected from the group consisting of a halogen atom, a cyano group, a bromo group, an iodine group, a hydroxy group, a C1 to C10 alkoxy group, a C1 to C10 ketone group, a C1 to C10 amine group, C30 alkyl group;
An amino group, an azine group, an azo group, an ureido group, an isocyanate group, an oxyimino group, a morpholinyl group, a piperazinyl group, a fluoro group, a chloro group, a bromo group, an iodo group, a hydroxy group, A C1 to C30 alkenyl group substituted or unsubstituted with at least one functional group selected from a C1 to C10 alkoxy group, a C1 to C10 ketone group, a C1 to C10 amine group, and a C1 to C10 ester group;
An amino group, an azine group, an azo group, an ureido group, an isocyanate group, an oxyimino group, a morpholinyl group, a piperazinyl group, a fluoro group, a chloro group, a bromo group, an iodo group, a hydroxy group, A C1 to C30 alkynyl group substituted or unsubstituted with at least one functional group selected from a C1 to C10 alkoxy group, a C1 to C10 ketone group, a C1 to C10 amine group, and a C1 to C10 ester group; or
An amino group, an azine group, an azo group, an ureido group, an isocyanate group, an oxyimino group, a morpholinyl group, a piperazinyl group, a fluoro group, a chloro group, a bromo group, an iodo group, a hydroxy group, A C3 to C10 cycloalkyl group which is unsubstituted or substituted with at least one functional group selected from a C1 to C10 alkoxy group, a C1 to C10 ketone group, a C1 to C10 amine group, and a C1 to C10 ester group,
X 4 to X 6 are each independently substituted or unsubstituted with at least one functional group selected from the group consisting of a vinyl group, an acryl group, a methacryl group, a thiol group, a mercapto group, a C1 to C10 sulfur group, and a C6 to C20 aryl group; An unsubstituted C1 to C30 alkyl group;
A C1 to C30 alkenyl group substituted or unsubstituted with at least one functional group selected from a vinyl group, an acryl group, a methacryl group, a thiol group, a mercapto group, a C1 to C10 sulfur group, and a C6 to C20 aryl group;
A C1 to C30 alkynyl group substituted or unsubstituted with at least one functional group selected from a vinyl group, an acrylic group, a methacrylic group, a thiol group, a mercapto group, a C1 to C10 sulfur group, and a C6 to C20 aryl group; or
Is a C3 to C10 cycloalkyl group substituted or unsubstituted with at least one functional group selected from a vinyl group, an acryl group, a methacryl group, a thiol group, a mercapto group, a C1 to C10 sulfur group, and a C6 to C20 aryl group.
And M is Si, Ti, or a combination thereof.
Wherein the graphene-containing ceramic hybrid sol solution further comprises a first additive selected from an inorganic powder, an organic additive, or a combination thereof.
Wherein the organic additive is contained in an amount of 0.01 to 10 parts by weight based on 100 parts by weight of the graphene-containing ceramic hybrid sol solution.
The organic additive may be selected from the group consisting of a curing agent, a resin binder, a monomer, a dispersant, a dispersion stabilizer, a surfactant, a polyimide precursor, an organic solvent, an amphoteric solvent, a hydrophilic solvent, A coupling agent, a thermoplastic resin, a conductive polymer, or a combination thereof.
And a second ceramic hybrid coating film disposed on at least one side of the first ceramic hybrid coating film,
Wherein the second ceramic hybrid coating film comprises graphene, a resin binder, an organic solvent, and an organosilane compound,
Wherein the content of graphene in the first ceramic hybrid coating film is different from the content of graphene in the second ceramic hybrid coating film.
Wherein the content of graphene in the second ceramic hybrid coating film is 0.001 wt% to 10 wt% with respect to the total weight of the second ceramic hybrid coating film.
The second ceramic hybrid coating may be selected from organic additives, nanoparticles, ceramics, dispersants, nanowires, carbon nanotubes, quantum dots, metals, salts, semiconductors, semiconducting materials, binders, monomers, silanes, polymers, And a second additive.
Wherein the second additive is included in an amount of 0.01 to 10 parts by weight based on 100 parts by weight of the second ceramic hybrid coating.
Wherein the nanoparticles are selected from the group consisting of SiO 2 ; Dispersed silica sol; Dispersed silica solution; A surface-modulated SiO 2 and an oxide of Al 2 O 3 , Li 4 Ti 5 O 12 , TiO 2 , SnO 2 , CeO 2 , ZrO 2 , V 2 O 5 , B 2 O 3 , BaTiO 3 , Y 2 O 3 , WO 3, MgO, CuO, ZnO, AlPO 4, AlF, Si 3 N 4, AlN, TiN, WC, SiC, TiC, MoSi 2, Fe 2 O 3, GeO 2, Li 2 O, MnO, NiO, zeolites, hollow Ceramics, and mixed dispersion sols of these; A surface-modulated SiO 2 and an oxide of Al 2 O 3 , Li 4 Ti 5 O 12 , TiO 2 , SnO 2 , CeO 2 , ZrO 2 , V 2 O 5 , B 2 O 3 , BaTiO 3 , Y 2 O 3 , WO 3, MgO, CuO, ZnO, AlPO 4, AlF, Si 3 N 4, AlN, TiN, WC, SiC, TiC, MoSi 2, Fe 2 O 3, GeO 2, Li 2 O, MnO, NiO, zeolites, hollow A ceramic hybrid, a mixed dispersion thereof, and a combination thereof.
The mixture is subjected to hydrolysis and polycondensation reaction to prepare a graft-containing ceramic hybrid sol solution,
Coating the ceramic hybrid sol solution on a substrate, drying the ceramic hybrid sol solution at a temperature of 25 ° C to 400 ° C, and heat treating the dried film at a temperature of 50 ° C to 900 ° C to form a coating film. As a method,
Wherein the ceramic hybrid coating film has a water droplet contact angle of 20 DEG or less, or 60 DEG or more.
[Chemical Formula 1]
X a n -M- (OH) 4-n
(2)
X b n -M- (OH) 4-n
In the above Formulas 1 and 2,
M is selected from Si, Ti, Ag, Sn, In, Zn, and combinations thereof,
X a represents an epoxy group, a glycidoxy group, a carboxyl group, an amino group, an azo group, an azo group, an ureido group, an isocyanate group, an oxyimino group, a morpholinyl group, a piperazinyl group, a fluoro group, a chloro group, , A C1 to C30 alkyl group substituted or unsubstituted with at least one functional group selected from a hydroxyl group, a C1 to C10 alkoxy group, a C1 to C10 ketone group, a C1 to C10 amine group, and a C1 to C10 ester group;
An amino group, an azine group, an azo group, an ureido group, an isocyanate group, an oxyimino group, a morpholinyl group, a piperazinyl group, a fluoro group, a chloro group, a bromo group, an iodo group, a hydroxy group, A C1 to C30 alkenyl group substituted or unsubstituted with at least one functional group selected from a C1 to C10 alkoxy group, a C1 to C10 ketone group, a C1 to C10 amine group, and a C1 to C10 ester group;
An amino group, an azine group, an azo group, an ureido group, an isocyanate group, an oxyimino group, a morpholinyl group, a piperazinyl group, a fluoro group, a chloro group, a bromo group, an iodo group, a hydroxy group, A C1 to C30 alkynyl group substituted or unsubstituted with at least one functional group selected from a C1 to C10 alkoxy group, a C1 to C10 ketone group, a C1 to C10 amine group, and a C1 to C10 ester group; or
An amino group, an azine group, an azo group, an ureido group, an isocyanate group, an oxyimino group, a morpholinyl group, a piperazinyl group, a fluoro group, a chloro group, a bromo group, an iodo group, a hydroxy group, A C3 to C10 cycloalkyl group which is unsubstituted or substituted with at least one functional group selected from a C1 to C10 alkoxy group, a C1 to C10 ketone group, a C1 to C10 amine group, and a C1 to C10 ester group,
X b is a C1 to C30 alkyl group substituted or unsubstituted with at least one functional group selected from a vinyl group, an acryl group, a methacryl group, a thiol group, a mercapto group, a C1 to C10 sulfur group, and a C6 to C20 aryl group ;
A C1 to C30 alkenyl group substituted or unsubstituted with at least one functional group selected from a vinyl group, an acryl group, a methacryl group, a thiol group, a mercapto group, a C1 to C10 sulfur group, and a C6 to C20 aryl group;
A C1 to C30 alkynyl group substituted or unsubstituted with at least one functional group selected from a vinyl group, an acrylic group, a methacrylic group, a thiol group, a mercapto group, a C1 to C10 sulfur group, and a C6 to C20 aryl group; or
A C3 to C10 cycloalkyl group which is substituted or unsubstituted with at least one functional group selected from a vinyl group, an acryl group, a methacryl group, a thiol group, a mercapto group, a C1 to C10 sulfur group, and a C6 to C20 aryl group,
n is an integer of 1 to 3;
A ceramic hybrid coating film for mixing the dispersed graphene oxide (RGO) in an amount of 0.001 wt% to 10 wt% and mixing the precursor of the hydrophilic hydrate represented by the formula (1) in an amount of 0.001 wt% to 10 wt% As a production method,
Wherein the ceramic hybrid coating film has a water droplet contact angle of 12 DEG or less.
A process for producing a ceramic hybrid coating film in which 0.001 to 10% by weight of the reduced graphene oxide (RGO) is mixed and 0.001 to 10% by weight of a precursor of the hydrophobic hydrate represented by the formula (2) As a result,
Wherein the ceramic hybrid coating film has a water droplet contact angle of 90 DEG or more.
Wherein the graphene dispersion treatment is performed by a mechanical dispersion treatment or a solvent substitution method.
In the solvent substitution method,
Mixing a graphene powder, a first dispersant, and a first non-aqueous solvent to prepare a dispersion comprising a graphene-first dispersant and a first non-aqueous solvent;
Adding a precursor of a second non-aqueous solvent and a hydrate to the dispersion to prepare a mixture; And
Mixing the mixture with a second dispersant and water to prepare a coating composition for forming a graphene-containing organic-inorganic ceramic hybrid sol
Wherein the ceramic hybrid coating film is formed on the surface of the ceramic hybrid coating film.
Wherein the content of graphene in the first ceramic hybrid coating film is different from the content of graphene in the second ceramic hybrid coating film.
Wherein the content of graphene in the second ceramic hybrid coating film is 0.001 wt% to 10 wt% with respect to the total weight of the second ceramic hybrid coating film.
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