KR101755101B1 - Surface protecting uv-curable coating composition - Google Patents
Surface protecting uv-curable coating composition Download PDFInfo
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- KR101755101B1 KR101755101B1 KR1020150088445A KR20150088445A KR101755101B1 KR 101755101 B1 KR101755101 B1 KR 101755101B1 KR 1020150088445 A KR1020150088445 A KR 1020150088445A KR 20150088445 A KR20150088445 A KR 20150088445A KR 101755101 B1 KR101755101 B1 KR 101755101B1
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Classifications
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- C—CHEMISTRY; METALLURGY
- 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
- C09D4/00—Coating compositions, e.g. paints, varnishes or lacquers, based on organic non-macromolecular compounds having at least one polymerisable carbon-to-carbon unsaturated bond ; Coating compositions, based on monomers of macromolecular compounds of groups C09D183/00 - C09D183/16
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- C—CHEMISTRY; METALLURGY
- 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
- C09D175/00—Coating compositions based on polyureas or polyurethanes; Coating compositions based on derivatives of such polymers
- C09D175/04—Polyurethanes
- C09D175/06—Polyurethanes from polyesters
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- C09D7/1233—
Abstract
The present invention relates to an ultraviolet ray curing type coating composition for protecting a plastic surface with enhanced abrasion resistance and scratch resistance. The ultraviolet ray curing type coating composition according to the present invention is excellent in adhesion and heat resistance to a plastic material, particularly a polycarbonate (PC) It has excellent abrasion resistance, scratch resistance, chipping resistance and chemical resistance, and has excellent weather resistance under ultraviolet light and visible light environment. Therefore, even when exposed to extreme outdoor conditions, there is no change in appearance such as discoloration or crack, It is very useful for surface coating of transparent materials such as plastic lenses, especially PC lenses of automobile headlamps.
Description
The present invention relates to an ultraviolet ray curing coating composition for surface protection, and more particularly to a ultraviolet ray curable coating composition for protecting a plastic surface having enhanced abrasion resistance and scratch resistance.
The conventional automotive headlamp market used glass as a headlamp cover. However, in order to improve the fuel efficiency of the automobile, the headlamp cover is made of plastic, especially polycarbonate, which is excellent in transparency and moldability.
Generally, polycarbonate applied to automobile headlamp lens is excellent in transparency and elasticity. However, scratch and abrasion against external impact is weaker than conventional glass, and appearance change due to acid rain and pollutants under external environment, Ultraviolet ray Visible light causes discoloration and cracking. Therefore, in order to compensate for the scratch resistance and weatherability, which is a weak point of the polycarbonate material, a hard coating coating process which is coated with a coating composition excellent in weatherability and scratch resistance is required.
The ultraviolet curable coating composition for plastic surface protection is applied to plastic materials to prevent discoloration and cracking after exposure to ultraviolet rays and visible light, and to protect the material from external impacts. Accordingly, the composition should be excellent in adhesion to a material, heat resistance, weather resistance, and especially abrasion resistance, chipping resistance and scratch resistance.
An example of using a polyfunctional urethane acrylate oligomer for improving scratch resistance is disclosed in Korean Patent Publication No. 10-0199908. However, when exposed to a long-term outdoor environment due to shrinkage stress between molecules in the coating film, cracks and yellowing of the coating film occur severely, resulting in deterioration of the appearance of the coating film, deterioration of adhesion and discoloration.
Korean Patent Laid-Open Publication No. 10-1999-0073009 discloses a coating composition using a urethane acrylate oligomer or an unreactive thermoplastic acrylic resin. However, in the case of this composition, since the scratch resistance and the heat resistance are lowered, There is a problem that can not be done.
Conventionally, hindered amine or benzotriazole light stabilizers have been used alone or in combination in coating compositions in order to achieve weatherability. In this case, when the composition is left for a long time under ultraviolet light and visible light, Migration and extraneous impact cause elution in the cracked coating film, and the weatherability is rapidly deteriorated.
Korean Patent Laid-Open Publication No. 10-2012-0097817 discloses a coating composition using a benzotriazole modified aliphatic urethane acrylate oligomer prepared by introducing benzotriazole into a urethane acrylate oligomer. However, this coating composition needs to be further improved in terms of abrasion resistance and scratch resistance.
The present invention relates to a plastic substrate, particularly a head lamp, which is excellent in adhesion to a plastic material, particularly a polycarbonate (PC) material, chipping resistance, heat resistance and weatherability, and particularly excellent in abrasion resistance and scratch resistance. The present invention provides an ultraviolet ray curable coating composition which can protect a material when applied to a plastic material for a glass substitute such as a PC lens.
(B) a benzotriazole modified acrylate or benzotriazole modified aliphatic urethane acrylate oligomer, (C) a polyfunctional aliphatic urethane acrylate oligomer having at least six polymerizable functional groups, (D) a nanosilane resin, (E) a photopolymerization initiator, (F) an ultraviolet absorber, and (G) a light stabilizer.
The ultraviolet ray curable coating composition according to the present invention is excellent in adhesion and heat resistance to a plastic material, particularly a polycarbonate (PC) material, and excellent in abrasion resistance, scratch resistance, chipping resistance and chemical resistance against external impact and environment , It is excellent in weatherability under ultraviolet rays and visible light environment. Therefore, it does not change appearance such as discoloration and cracks even under severe outdoor use conditions, and is very suitable for surface coating of transparent plastic lenses such as PC lenses of automobile head lamps useful.
Hereinafter, the present invention will be described in more detail.
Multifunctional Aliphatic urethane Acrylate Oligomer [Component (A)]
The polyfunctional aliphatic urethane acrylate oligomer contained in the ultraviolet curable coating composition of the present invention has 6 or more (for example, 6 to 15) polymerizable functional groups which are unsaturated groups capable of polymerization and is used for scratch resistance and hardness of the coating film Lt; / RTI >
The weight average molecular weight of the polyfunctional aliphatic urethane acrylate oligomer may be from 1000 to 2000.
If the number of the polymerizable functional groups in one molecule of the polyfunctional aliphatic urethane acrylate oligomer is less than 6, the hardness of the coating film becomes weak and it is difficult to obtain a coating film having a pencil hardness of 2H or more, and the scratch resistance property in the steel wool is deteriorated.
Examples of the polyfunctional aliphatic urethane acrylate oligomer include an unsaturated group capable of polymerization with a bifunctional aliphatic isocyanate compound (for example, hexamethylene diisocyanate, dicyclohexylmethane diisocyanate, isophorone diisocyanate, etc.) (For example, pentaerythritol triacrylate, dipentaerythritol triacrylate and the like) having 3 or more per molecule can be used. Specific examples thereof include PU610, SK- Ebecryl 1290 from Cytec, U400 from Bayer, DM 87A from Double Bond Chemical, and the like.
The ultraviolet ray curable coating composition of the present invention may contain the component (A) in an amount of 30 to 60% by weight or 35 to 55% by weight based on 100% by weight of the total composition components excluding the organic solvent. If the content of the component (A) in the composition is too small, the formation of a cured coating film is difficult and the curability and scratch resistance are poor. On the other hand, if the content is too high, excessive curing density may cause cracks in the coating film.
Benzotriazole denaturalization Acrylate or Benzotriazole Modified aliphatic urethane Acrylate Oligomer [Component (B)]
In the present invention, component (B) is a component used for weather resistance and oxidation resistance of a coating film.
As the benzotriazole-modified acrylate, those having a molecular weight in the range of 300 to 500 can be used when considering weatherability and oxidation resistance, particularly compatibility and transparency. When the benzotriazole modified acrylate deviating from the molecular weight range is used, transparency and compatibility may be lowered, and discoloration of the coating composition may be caused.
The benzotriazole modified aliphatic urethane acrylate oligomer is produced by the reaction of a benzotriazole having a hydroxy group with an isocyanate and an acrylate compound, and may have a weight average molecular weight of 800 to 1,500.
Examples of the benzotriazol-modified aliphatic urethane acrylate oligomer include unsaturated aliphatic urethane acrylate oligomers capable of being polymerized with a bifunctional aliphatic isocyanate compound (for example, hexamethylene diisocyanate, dicyclohexylmethane diisocyanate, isophorone diisocyanate, etc.) (E.g., hydroxyethyl acrylate, hydroxypropyl acrylate, hydroxyethyl methacrylate, hydroxybutyl acrylate, hydroxypentyl acrylate, hydroxypropyl acrylate, hydroxypropyl acrylate, , Hydroxybutyl methacrylate, etc.) with an aliphatic urethane acrylate oligomer and a benzotriazole modified acrylate having a hydroxy group can be used.
The ultraviolet ray curable coating composition of the present invention may contain the component (B) in an amount of 3 to 20% by weight or 5 to 15% by weight based on 100% by weight of the total composition components excluding the organic solvent. If the content of the component (B) in the composition is too small, the weather resistance and oxidation resistance of the coating film tends to be deteriorated. On the other hand, if the content is too high, discoloration of the coating film due to uncured coating film and characteristics of the resin itself may be caused.
Multifunctional Acrylate The monomer [Component (C)]
The multifunctional acrylate monomer contained in the ultraviolet curable coating composition of the present invention is an acrylate monomer containing two or more (for example, 2 to 6) polymerizable unsaturated groups per molecule, and the scratch resistance, hardness , A component used for adhesion, and for the purpose of assisting the curing properties by reacting with the resin composition.
Examples of the polyfunctional acrylate monomers include butanediol diacrylate, 1,6-hexanediol diacrylate, 1,6-hexanediol dimethacrylate, neopentyl glycol diacrylate, triethylene glycol diacrylate , Tetraethylene glycol diacrylate, tripropylene glycol diacrylate, trimethylolpropane triacrylate, pentaerythritol triacrylate, and glyceryl propoxy triacrylate. These may be used alone or in combination of two or more Can be used.
The ultraviolet ray curable coating composition of the present invention may contain the component (C) in an amount of 5 to 40% by weight or 25 to 35% by weight based on 100% by weight of the total composition components excluding the organic solvent. If the content of the component (C) in the composition is too small, the viscosity of the paint increases, the adhesion to the substrate becomes poor, and the abrasion resistance and scratch resistance may deteriorate. Conversely, if too large, the hardenability and scratch resistance , And ultraviolet curing may cause clouding of the film in the long term due to the presence of unreacted material.
Nano Silane Resin [Component (D)]
The nano-silane resin contained in the ultraviolet curable coating composition of the present invention is produced by the reaction of an organic compound having a polymerizable double bond (for example, acrylate or methacrylate or a derivative thereof) with nano-sized silica, Is a component used for improving abrasion resistance and scratch resistance.
The particle size of the silica in the nanosilane resin may be 10 to 100 nm or 10 to 50 nm. If the particle size of the silica is less than 10 nm, it is difficult to exhibit the abrasion resistance and scratch resistance to be realized. On the other hand, when the particle size exceeds 100 nm, the permeability of the coating film is lowered, and haze and surface smoothness of the coating film may be lowered.
The nanosilane resin may be, for example, acryloyl- or methacryloyl-modified nanosilica obtained by reacting acrylate or methacrylate with nano-sized silica. Specific examples thereof include TOCOSEI's MAC-SQ HDM But is not limited thereto.
The ultraviolet ray curable coating composition of the present invention may contain the component (D) in an amount of 5 to 25% by weight or 7 to 20% by weight based on 100% by weight of the total composition components excluding the organic solvent. If the content of the component (D) in the composition is less than 5% by weight, the abrasion resistance and scratch resistance of the coating film tends to be deteriorated. On the other hand, if it exceeds 25% by weight, ultraviolet rays are scattered by silica to cause poor coating film hardness, .
Light curing Initiator [Component (E)]
The photopolymerization initiator contained in the ultraviolet curing type coating composition of the present invention is used for curing the film forming component, and examples thereof include 2-hydroxy-2-methyl-1-phenylpropane-1-phenone, 1- hydroxycyclohexylphenyl Ketone, benzophenone, 1- (4-isopropylphenyl) 2-hydroxy 2-methyl 1-one, 1- [4- (2- hydroxyethoxy) phenyl] -2- (2,4,6-trimethylbenzoyl) -phenylphosphine oxide, and the like can be used singly or in combination of two or more kinds, such as 1-on, alpha, alpha -diethoxyacetophenone, 2,2- Can be used in combination.
The photopolymerization initiator preferably absorbs light having a wavelength of 230 to 280 nm and a wavelength of 300 to 380 nm. If the photopolymerization initiator does not absorb light having a wavelength of 230 to 280 nm, deterioration of the appearance and scratch may occur due to peeling of the coating film, difference in hardness between the surface and the inside of the coating film, and scattering by the inorganic material if the light of 300 to 380 nm wavelength is not absorbed The hardenability may be lowered.
The ultraviolet ray curable coating composition of the present invention may contain the component (E) in an amount of 1 to 10% by weight or 1 to 5% by weight based on 100% by weight of the total composition components excluding the organic solvent. If the content of the component (E) in the composition is too small, the curability may be deteriorated and the scratch resistance and adhesion may be deteriorated due to uncured. On the contrary, if the content is too high, contamination due to unreacted photopolymerization initiator, Yellowing may occur.
Ultraviolet absorber [Component (F)]
The ultraviolet absorbent contained in the ultraviolet curable coating composition of the present invention is used for improving the weather resistance of the cured coating film and the durability of the plastic material.
Examples of the ultraviolet absorber include triazine-based compounds such as, but not limited to, 6- [bis (2,4-dimethylphenyl) -1,3,5-triazine, tris - [2- {4- (octyl-2-methylethanoate) oxy-2-hydroxyphenyl}] - 1,3,5 triazine and the like can be used alone or in combination of two or more.
In the ultraviolet curable coating composition of the present invention, the component (F) may be contained in an amount of 0.5 to 10% by weight or 0.75 to 8% by weight based on 100% by weight of the total composition components excluding the organic solvent. When the content of the component (F) in the composition is too small, the weatherability is lowered, and deterioration of the coating film and yellowing, cracking, etc. may occur in a long-term outdoor environment. On the contrary, if it is too much, the photocuring reaction is deteriorated, And can cause cloudiness.
Light stabilizer [Ingredient (G)]
The light stabilizer (or antioxidant) contained in the ultraviolet curable coating composition of the present invention is used to improve the weatherability of the cured coating film and the durability of the plastic material.
As the light stabilizer, hindered amine light stabilizers (HALS) may be used singly or in combination of two or more. Examples thereof include, but are not limited to, bis (1-methoxy- 6,6-tetramethyl-4-piperidyl) sebacate can be used.
The ultraviolet ray curable coating composition of the present invention may contain the component (G) in an amount of 0.1 to 5% by weight or 0.2 to 2.5% by weight based on 100% by weight of the total composition components excluding the organic solvent. If the content of the component (G) in the composition is too small, the weatherability may deteriorate and deterioration of the coating film and yellowing or cracking may occur in a long-term outdoor environment. On the other hand, if it is too much, the photocuring reaction is deteriorated, And can cause cloudiness.
The ultraviolet ray curable coating composition of the present invention may further contain a solvent, a wetting agent, a leveling agent, an antifoaming agent, etc., which are usually added to the coating composition, in addition to the above components. These additional components can enhance the workability of the coating and the smoothness of the coating.
Examples of usable solvents in the present invention include ketones such as acetone, acetates such as ethyl acetate, and aromatic solvents such as toluene. When the solvent is used, the content thereof may be 30 to 80% by weight based on 100% by weight of the total amount of the coating composition. If the solvent content is too low, workability and leveling may be deteriorated, and if too large, the coating film formation tends to be deteriorated.
Examples of the wetting agent that can be used in the present invention include polyether-modified polydimethylsiloxane, dimethylpolysiloxane as a defoaming agent, and silicon diacrylate-based or silicone polyacrylate-based compounds as a leveling agent. It is preferable that the content is not more than 1% by weight based on 100% by weight.
There is no particular limitation on the method for producing the ultraviolet ray curable coating composition of the present invention. For example, the components (A) to (G) as described above may be mixed with a diluting agent, a surface modifying additive, , And then mixed at an appropriate temperature (for example, room temperature).
According to another aspect of the present invention, there is provided a molded article comprising a cured coating layer formed from the ultraviolet curable coating composition of the present invention as described above.
Plastics (for example, polycarbonate (PC)) are preferable as the material of the molded article to which the ultraviolet ray curable coating composition of the present invention can be applied. According to a preferred embodiment of the present invention, the UV curable coating composition of the present invention is coated on the surface of a molded article of this material, dried by solvent, and cured by ultraviolet irradiation to form a hard coating layer for protecting the surface of the molded article. The ultraviolet ray curable coating composition of the present invention is preferably applied to a molded article for an automobile, more preferably a PC lens for an automobile head lamp. It can also be used in building materials and exterior plastics to replace glass.
Hereinafter, the present invention will be described in more detail with reference to examples and comparative examples. However, the scope of the present invention is not limited thereto.
[ Example ]
Preparation of Coating Composition
UV-curable coating compositions of Examples and Comparative Examples were prepared in the compositions shown in Table 1 below.
A: A hexafunctional aliphatic urethane acrylate oligomer having a molecular weight of about 1800, which was obtained by reacting isophorone diisocyanate with pentaerythritol triacrylate
B: Benzotriazole modified acrylate monomer
C1: bifunctional acrylate monomer [1,6-hexanediol diacrylate]
C2: 6-functional acrylate monomer [dipentaerythritol hexaacrylate]
D1: Methacryloyl-modified silica (silica particle size: 20 nm)
D2: Methacryloyl-modified silica (silica particle size: 10 nm)
D3: Methacryloyl-modified silica (silica particle size: 100 nm)
D4: colloidal silica (particle size: 5 nm) [D4 is added to the above C1 (1,6-hexanediol diacrylate) after dispersing with a dispersant (BYK 103)
D5: colloidal silica (particle size: 120 nm)
D6: silica (particle size: 3-5 nm)
E: IRGACURE 184
F: Hydroxyphenyltriazine based UV absorber
G: Hindered amine light stabilizer (HALS)
Solvent: Methoxypropanol
Evaluation of Physical Properties of Coating Composition
The ultraviolet curable coating compositions prepared in the above Examples and Comparative Examples were air-spray coated on a transparent polycarbonate specimen (trade name: LS2-111, SABIC) at a thickness of about 10 microns (top layer, dry film thickness) , The solvent was removed, and the hard coated specimen was cured by irradiation with energy of 3500 mJ / cm 2 at a position of about 20 cm in air with a high pressure mercury lamp of 300 mW / cm 2 to evaluate the following items The results are shown in Table 2 below.
One) Attachment
A cross-cut tape test was conducted according to ASTM D3359
2) Pencil Hardness
According to ISO 15184 and JIS K 5600-5-4, it should be H or higher. [Passed both the example and the comparative example]
3) Scratch resistance
Steel wool # 0000 grade was used to check the film damage after rubbing 20 times with a force of 4.9 N [O: excellent, △: normal, X: poor]
4) Moisture resistance
The sample was allowed to stand for 240 hours under the conditions of a test temperature and a relative humidity of 98 ± 2%, and the sample was allowed to stand for 1 hour to observe a remarkable discoloration, fading, swelling, Evaluation of abnormality [O: excellent,?: Normal, X: poor]
5) Water resistance
The specimens were immersed in tap water (TAP WATER, test temperature: 40 ° C) for 240 hours, removed from the surface by air blow, and left for 1 hour at room temperature. The discoloration, fading, swelling, And evaluated whether there is no deterioration or adherence [O: excellent,?: Normal, X: poor]
6) Heat resistance
After leaving for 300 hours at the test temperature (80 ± 2 ° C), it was taken out and left at room temperature for 1 hour. Thereafter, it was evaluated whether there was no discoloration, discoloration, swelling, Good, △: fair, X: poor)
7) Chemical resistance
Glass cleaner and engine oil were separately used and then reciprocated 20 times with a force of 3N. Then, the surface of the coating was rubbed and the appearance was visually observed. After standing for 24 hours at room temperature, significant discoloration, fading, swelling, And evaluated whether there is no abnormality in adhesion [O: excellent,?: Normal, X: poor]
8) My cold heat Cycle Castle
The test piece was allowed to stand at 80 ± 2 ° C for 3 hours, left at room temperature for 1 hour, left at -40 ° C for 3 hours, left at room temperature for 1 hour, 7 ± 15 hours at 50 ± 2 ° C, 95% RH) Evaluation was made as to whether or not there was any discoloration, fading, swelling, cracking, gloss reduction, or the like in the coating film at the time of observation. [O: Excellent,?: Normal, X: Bad]
9) Promoting weatherability
Five test specimens were simultaneously irradiated under the following conditions of Xenon arc condition specified in SAE J 2527, and there was no discoloration (color difference (ΔE)), discoloration, swelling, cracking, (ΔE: more than 3.0, crack occurred) [Evaluation: O: excellent (ΔE: not more than 3.0, no crack occurred)
Xenon Acro set conditions:
4000 KJ / m < 2 > [340 nm]
BLACK PNL Temperature - (LIGHT) 38 ± 2 ℃ (DARK) 40 minutes irradiation (50 ± 5% RH)
Cycle - 60 minutes irradiation (50 ± 5% RH) 60 minutes irradiation (95 ± 5% RH, surface / back SPRAY)
Irradiation illuminance - 0.55 0.02 W / (m 2 nm m) [340 nm]
10) Chipping resistance
The test piece was subjected to a chipping resistance test under the following conditions by a non-stoker (GRAVELO METER: SAE J 400 standard product) for the test. Thereafter, evaluation was made as to whether there was any remarkable cracking, : Normal, X: Bad]
Chipping resistance test conditions:
Shooting Distance: 150mm
Shooting Angle: 45 °
Shooting Pressure: 3.0 Kgf / cm 2
Test Temperature: -40 ° C
Grain: 50 g (JIS Crushed gravel No. 7 stone, 2.5 to 5 mm, 350 to 400 pieces)
11) Abrasion resistance
The test specimens were evaluated by measuring the change in haze value (ΔH) between the beginning and after the test with a SPECTROPHOTOMETER (target mask 25.3 mm) under 500 g load and 500 cycles of abrasive wheels CS-10F on a Taber Abraser tester [O: Excellent : DELTA: normal (DELTA H: more than 15 to 25), X: defective (DELTA H: more than 25)
12) Appearance
The haze value of the test piece was measured with SPECTROPHOTOMETER (target mask 25.3 mm) [O: excellent appearance (initial haze: 0 to 0.5), C: appearance (Initial haze: more than 0.5 to 0.7), X: poor appearance (initial haze: more than 0.7)]
Claims (8)
(B) a benzotriazole modified acrylate or benzotriazole modified aliphatic urethane acrylate oligomer,
(C) a polyfunctional acrylate monomer,
(D) a nanosilane resin,
(E) a photopolymerization initiator,
(F) ultraviolet absorber and
(G) light stabilizer,
The nanosilane resin is a methacryloyl-modified nanosilica produced by reacting methacrylate with nano-sized silica,
A UV curable coating composition for automotive headlamp cover coating.
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| KR1020150088445A KR101755101B1 (en) | 2015-06-22 | 2015-06-22 | Surface protecting uv-curable coating composition |
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| KR101755101B1 true KR101755101B1 (en) | 2017-07-07 |
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| KR102166449B1 (en) * | 2018-12-31 | 2020-10-15 | 주식회사 케이씨씨 | Curable Coating Composition |
| KR102563668B1 (en) * | 2020-12-18 | 2023-08-04 | 홍익대학교 산학협력단 | Boundary stone attachment cover with excellent retro-reflective properties, and manufacturing method thereof |
Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| KR100856431B1 (en) * | 2007-05-28 | 2008-09-04 | (주)엔피케미칼 | Uv curable hard coating composition for blue-ray disc |
| KR101184448B1 (en) | 2008-12-29 | 2012-09-20 | 제일모직주식회사 | Uv curing hard coating composition, polarizing film having anti-smudge using the composition and method of manufacturing hard coating layer |
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| KR100856431B1 (en) * | 2007-05-28 | 2008-09-04 | (주)엔피케미칼 | Uv curable hard coating composition for blue-ray disc |
| KR101184448B1 (en) | 2008-12-29 | 2012-09-20 | 제일모직주식회사 | Uv curing hard coating composition, polarizing film having anti-smudge using the composition and method of manufacturing hard coating layer |
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