WO2018143539A1 - Composition de revêtement dur, et film de revêtement dur utilisant celle-ci - Google Patents

Composition de revêtement dur, et film de revêtement dur utilisant celle-ci Download PDF

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Publication number
WO2018143539A1
WO2018143539A1 PCT/KR2017/011966 KR2017011966W WO2018143539A1 WO 2018143539 A1 WO2018143539 A1 WO 2018143539A1 KR 2017011966 W KR2017011966 W KR 2017011966W WO 2018143539 A1 WO2018143539 A1 WO 2018143539A1
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hard coating
meth
coating composition
acrylate
group
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PCT/KR2017/011966
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English (en)
Korean (ko)
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이승우
안홍준
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동우화인켐 주식회사
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Publication of WO2018143539A1 publication Critical patent/WO2018143539A1/fr

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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
    • 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
    • C09D7/00—Features of coating compositions, not provided for in group C09D5/00; Processes for incorporating ingredients in coating compositions
    • C09D7/40—Additives
    • C09D7/47—Levelling agents
    • 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
    • C09D7/00—Features of coating compositions, not provided for in group C09D5/00; Processes for incorporating ingredients in coating compositions
    • C09D7/40—Additives
    • C09D7/48—Stabilisers against degradation by oxygen, light or heat
    • 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
    • C09D7/00—Features of coating compositions, not provided for in group C09D5/00; Processes for incorporating ingredients in coating compositions
    • C09D7/40—Additives
    • C09D7/60—Additives non-macromolecular
    • C09D7/61—Additives non-macromolecular inorganic
    • 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
    • C09D7/00—Features of coating compositions, not provided for in group C09D5/00; Processes for incorporating ingredients in coating compositions
    • C09D7/40—Additives
    • C09D7/60—Additives non-macromolecular
    • C09D7/63—Additives non-macromolecular organic
    • G—PHYSICS
    • G02—OPTICS
    • G02B—OPTICAL ELEMENTS, SYSTEMS OR APPARATUS
    • G02B1/00—Optical elements characterised by the material of which they are made; Optical coatings for optical elements
    • G02B1/10—Optical coatings produced by application to, or surface treatment of, optical elements

Definitions

  • the present invention relates to a hard coating composition capable of forming a hard coating film for protecting a display of an image display device and a hard coating film formed therefrom.
  • the foldable display is a display that can be folded in half like a book or a notebook, and various technologies and patents have been proposed by various companies.
  • the display When the display is designed to be foldable, it can be used as a tablet when it is unfolded and a smartphone can be used when it is folded, so that displays of different sizes can be used as one product, and larger sizes like tablets or TVs than smaller smartphones.
  • the device In the case of the device can be folded to carry and carry convenience can be doubled.
  • a cover window made of glass is provided at the outermost part of the display to protect the display.
  • glass is not applicable to the foldable display, and a high hardness hard coating film having high hardness and wear resistance is used to replace the glass.
  • the thickness of the hard coating layer in the hard coating film must be thickened. As the thickness of the hard coating layer increases, the surface hardness can be increased, but the wrinkles and curls increase due to hardening shrinkage of the hard coating layer. It is not easy to apply practically because cracks (or cracks) or peeling of the coating layer tend to occur.
  • a method for improving abrasion resistance and scratch resistance a method of adding a fine-powder inorganic filler or colloidal silica is usually known.
  • a method of adding an inorganic filler or silica stability problems due to precipitation and gel generation of colloidal silica particles whose silica surface has been modified with organic matter or silane have arisen, and the degree of curing of the film, optical transparency and adhesion
  • wear resistance, scratch resistance, and the like do not meet the requirements of the hard coating film for display device protection.
  • Republic of Korea Patent Publication No. 2011-0043234 relates to a UV-curable coating composition, UV-curable coating composition comprising at least six functional polyester acrylate oligomer, bifunctional urethane acrylate oligomer, at least one photocurable monomer and photoinitiator Disclosed information about.
  • the Republic of Korea Patent Publication No. 2016-0100121 relates to a hard coating composition and a hard coating film using the same, a polyfunctional urethane (meth) having a polyfunctional (meth) acrylate (A) having a ethylene glycol group and a cyclohexyl group
  • An acrylate monomer mixture comprising a acrylate (B), a photoinitiator and a solvent, wherein the acrylate monomer mixture discloses a content of a hard coating composition satisfying the formula (1).
  • Patent Document 1 Republic of Korea Patent Publication No. 2011-0043234 (2011.04.27.)
  • Patent Document 2 Republic of Korea Patent Publication 2016-0100121 (2016.08.23.)
  • An object of the present invention is to provide a hard coating composition capable of producing a hard coating film excellent in hardness, flexibility, wear resistance or scratch resistance.
  • an object of the present invention is to provide a hard coat film excellent in hardness, flexibility, wear resistance or scratch resistance.
  • Hard coating composition of the present invention for achieving the above object is a dendrimer comprising a (meth) acrylate end group; A fluorine-based polyfunctional (meth) acrylate compound including a urethane group represented by Formula 1 below; And inorganic nanoparticles.
  • n and m are each independently an integer of 1 to 10.
  • the present invention provides an image display device having a hard coat film described above.
  • the present invention provides a window of the display device provided with the hard coating film described above.
  • the hard coating composition according to the present invention includes a dendrimer having a specific structure, a fluorine-based polyfunctional (meth) acrylate-based compound including a urethane group, and inorganic nanoparticles, thereby providing excellent hardness and flexibility, and a hard coating film having excellent wear resistance and scratch resistance. Can be manufactured, and thus it is applicable to the window of the flexible display device as well as the image display device.
  • a member when a member is located "on" another member, this includes not only when one member is in contact with another member but also when another member exists between the two members.
  • One aspect of the present invention is a dendrimer comprising a (meth) acrylate end group; A fluorine-based polyfunctional (meth) acrylate compound including a urethane group represented by Formula 1 below; It relates to a hard coating composition comprising; and inorganic nanoparticles.
  • n and m are each independently an integer of 1 to 10.
  • the hard coating composition of the present invention is a polyfunctional (meth) acrylate containing an oxyethylene group, photoinitiator; solvent; And an additive selected from the group consisting of a leveling agent and a stabilizer.
  • the total solid content of the hard coating composition means the total content of the remaining components excluding the solvent from the hard coating composition.
  • inorganic nanoparticles when inorganic nanoparticles are dispersed, only inorganic nanoparticles are considered in the total solid content of the hard coating composition.
  • the hard coating composition of the present invention includes a dendrimer comprising a (meth) acrylate end group.
  • the dendrimer according to the present invention has a structure of two or more generations, and the branch end may be substituted with (meth) acrylate to be used for ultraviolet curing.
  • the branch end may be substituted with (meth) acrylate to be used for ultraviolet curing.
  • the general multifunctional acrylate monomer it has a structural feature that has more functional groups relative to the molecular weight according to the increase of generation, and may be due to the improvement of the bending property of the core part when the functional group is distributed at the end. Accordingly, when a dendrimer including a (meth) acrylate end group according to the present invention is included, there is an advantage in that the effect of a high hardness hard coat layer with improved curl and flexibility is obtained.
  • the dendrimer is represented by the following formula (2).
  • p is an integer from 2 to 4,
  • R1 is an alkyl group having 2 to 5 carbon atoms
  • R 3 is a moiety containing a hydrogen atom or a (meth) acrylate group, and at least one R 3 in the molecule is a moiety containing a (meth) acrylate group.
  • the dendrimer of Formula 2 is a second generation dendrimer.
  • the dendrimer including the (meth) acrylate end group according to the present invention preferably has a structure of two or more generations, and the branch end is substituted with (meth) acrylate. Because it can be used for ultraviolet curing, it can serve as a polymerizable compound in the hard coating composition.
  • Carbon number of the alkyl group in the present invention may be 1 to 10, preferably 1 to 6.
  • Specific examples include methyl, ethyl, propyl, n-propyl, isopropyl, butyl, n-butyl, isobutyl, tert-butyl, sec-butyl, 1-methyl-butyl, 1-ethyl-butyl, pentyl, n-pentyl , Isopentyl, neopentyl, tert-pentyl, hexyl, n-hexyl, 1-methylpentyl, 2-methylpentyl, 4-methyl-2-pentyl, 3,3-dimethylbutyl, 2-ethylbutyl, heptyl, n -Heptyl, 1-methylhexyl, cyclopentylmethyl, cyclohexylmethyl, octyl, n-octyl, tert-
  • R3 is a hydrogen atom or At least one R3 is And x is 2 or 3
  • R4 is a portion containing a hydrogen atom or a (meth) acrylate group, and at least one R4 in the molecule may be a portion containing a (meth) acrylate group.
  • the dendrimer of Formula 2 becomes a third generation dendrimer, and includes at least one (meth) acrylate group at a branch end, specifically, a (meth) acrylate group, thereby polymerizing in a hard coating composition.
  • a dendrimer compound is a compound in which a chain of molecules is regularly polymerized from the center to an outward direction according to a certain rule.
  • generation refers to a compound in which a polymerizable functional group undergoes a polymerization reaction based on the center to form a branch. Meaning, when the branched terminal of the first generation formed proceeds to the polymerization again, the second generation becomes, and the repeated polymerization proceeds.
  • p, q and x means the number of generations per generation, which means the number of polymerizable functional groups that the polymerization reaction can proceed in each generation, the total number of synthesized dendrimer multiplied by the number of generations per generation Means that.
  • the dendrimer represented by the formula (2) is a component for adjusting the molecular weight and the crosslinking density of the polymer in an appropriate range during the polymerization reaction of the polymerizable component of the hard coating composition, wherein the polymerizable component is the dendrimer, which will be described later And a photopolymerizable compound such as a polyfunctional (meth) acrylate containing an oxyethylene group which may be further included, and a fluorine-based polyfunctional (meth) acrylate-based compound including a urethane group represented by the formula (1).
  • the dendrimer of the formula (2) is polymerized so as to have a branch in the outward direction based on the center during the polymerization reaction, polymerizable functional groups are formed at each branch end. Accordingly, compared with the polymerization reaction of the polymerizable compound having a general structure, since the polymer has more functional groups compared to the molecular weight increase, it is possible to implement excellent hardness properties.
  • the dendrimer of the formula (2) since the dendrimer of the formula (2) includes a polymerizable functional group only at the terminal, the polymer core can secure appropriate flexibility, and thus, when included in the hard coating layer, it is possible to secure curl and improve curl characteristics and flexibility. .
  • a schematic polymerization scheme of the dendrimer is as follows.
  • the dendrimer according to one embodiment of the present invention forms a first generation dendrimer structure in which DMPA is condensed with TMP as the center. Thereafter, the generation of dendrimers is continuously increased by condensation polymerization of DMPA as a branched structure, and after the third generation, condensation polymerization of (meth) acrylic acid or the like at the terminal group forms a dendrimer having a polyfunctional (meth) acryl group at the terminal. It becomes possible.
  • the dendrimer represented by Chemical Formula 2 preferably has a second generation or third generation structure, and when the reaction proceeds for more than three generations, gelation may occur.
  • the dendrimer containing the (meth) acrylate end groups may be included in 10 to 60 parts by weight, preferably 15 to 55 parts by weight based on 100 parts by weight of the total hard coating composition. .
  • the dendrimer is included in less than the above range it may be somewhat difficult to impart the bending characteristics, if it exceeds the above range because the presence of unreacted functional groups due to the steric inhibition effect may be somewhat difficult to impart hardness characteristics to the hard coat layer, It is preferable to be included in the said range.
  • the hard coating composition according to the present invention includes a fluorine-based polyfunctional (meth) acrylate compound containing a urethane group represented by the following formula (1).
  • n and m are each independently an integer of 1 to 10.
  • the physical properties of the fluorine-based compound are mostly represented by the properties of the fluorine atom. Strong covalent bond between and carbon atoms. Covalent bonding force between the fluorine atom and the carbon atom is very strong compared to the bond between the carbon-carbon bonds and carbon-hydrogen bonds in general, thereby having excellent chemical resistance, durability and the like.
  • the three-dimensional structure between the carbon and fluorine has a slightly twisted spiral structure due to the repulsive force between the fluorine atoms, thereby protecting the carbon-carbon bond by the fluorine atom.
  • the fluorine-based compounds have properties such as low surface energy and low friction coefficient to the hard coating composition has the advantage that can contribute to the improvement of wear resistance.
  • the fluorine-based polyfunctional (meth) acrylate compound including the urethane group represented by Formula 1 is a monofunctional acrylate compound including an NCO group and a diol compound including a perfluoroether group formed through a urethane bond Can be.
  • the fluorine-based polyfunctional (meth) acrylate compound including the urethane group is a (meth) acrylate compound having an isocyanate group (Formula 3) and a diol compound having a perfluoroether group (Formula 4)
  • Butyl tin dilaurate (Dibutyltin dilaurate) in a 4-neck flask in a 2: 1 molar ratio can be obtained by stirring for 24 hours at 50 ° C conditions, but is not limited thereto.
  • the fluorine-based polyfunctional (meth) acrylate compound containing a urethane group represented by the formula (1) is 0.5 to 10 parts by weight, preferably 1 to 100 parts by weight of the total hard coating composition To 5 parts by weight.
  • the fluorine-based polyfunctional (meth) acrylate compound including the urethane group is included in the above range, there is an advantage in that the bending property is excellent while the wear resistance improving effect is excellent.
  • the fluorine-based polyfunctional (meth) acrylate compound including the urethane group is included in less than the above range may be ineffective wear resistance, if exceeding the above range because the bending characteristics of the coating film may be somewhat lowered, the above range It is preferable to use inside.
  • the fluorine-based polyfunctional (meth) acrylate compound according to the present invention includes a urethane group, it is advantageous in that it can be provided with excellent bending characteristics and wear resistance when it is included in a hard coating composition due to the structural characteristics caused by the urethane bond.
  • the hard coating composition according to the present invention includes inorganic nanoparticles.
  • the inorganic nanoparticles may further improve the mechanical properties of the hard coating composition.
  • the inorganic nanoparticles may be reactive inorganic nanoparticles.
  • the reactive inorganic nanoparticles may have a reactive functional group, and in this case, may participate in a photocuring reaction, thereby improving the mechanical properties.
  • the reactive functional group may be a vinyl group or a hydroxyl group such as acryloyl group, methacryloyl group or vinyl ether, but is not limited thereto.
  • the “reactive inorganic nanoparticles” may include at least a portion of the surface of the inorganic nanoparticles. It refers to a substituted with a functional group.
  • the inorganic nanoparticles having the reactive functional group may have a surface substituted with a (meth) acryl functional group, and in this case, the inorganic nanoparticles may have a characteristic of participating in a photocuring reaction.
  • the inorganic nanoparticles are uniformly formed in the coating film, thereby improving mechanical properties such as wear resistance, scratch resistance, and pencil hardness.
  • the material of the inorganic nanoparticles may be a metal oxide, for example, Al 2 O 3 , SiO 2 , ZnO, ZrO 2 , BaTiO 3 , TiO 2 , Ta 2 O 5 , Ti 3 O 5 , ITO, IZO, ATO,
  • a metal oxide for example, Al 2 O 3 , SiO 2 , ZnO, ZrO 2 , BaTiO 3 , TiO 2 , Ta 2 O 5 , Ti 3 O 5 , ITO, IZO, ATO
  • One kind selected from the group consisting of ZnO-Al, Nb 2 O 3 , SnO, MgO, and combinations thereof may be used, and preferably Al 2 O 3 , SiO 2 , ZrO 2, etc. may be used, but is not limited thereto. Does not.
  • the inorganic nanoparticles may have an average particle diameter of 1 to 100nm, preferably 5 to 50nm, in which case it is formed uniformly in the coating film to improve the mechanical properties such as wear resistance, scratch resistance, pencil hardness, etc. There is this. If the average particle diameter of the inorganic nanoparticles is less than the above range, aggregation may occur in the composition to form a uniform coating film, and if it exceeds the above range, the optical properties of the finally obtained coating film may be slightly reduced. Rather, since the problem may occur that the mechanical properties are lowered, it is preferable to use inorganic nanoparticles within the above range.
  • the inorganic nanoparticles may be purchased directly or manufactured and used, but is not limited thereto. Commercially available products can be used dispersed in a concentration of 10 to 80% by weight in an organic solvent, but is not limited thereto.
  • the inorganic nanoparticles are included in 5 to 40 parts by weight, preferably 10 to 35 parts by weight, more preferably 15 to 30 parts by weight based on 100 parts by weight of the total hard coating composition. Can be.
  • the inorganic nanoparticles are included in the above range, there is an advantage in that a hard coating film having excellent mechanical properties such as wear resistance, scratch resistance, and pencil hardness can be manufactured.
  • the mechanical properties such as wear resistance, scratch resistance, pencil hardness, etc. may not be sufficient, when the inorganic nanoparticles exceed the above range, the mechanical properties are lowered by hindering the curing properties, appearance This can lead to problems that can be bad.
  • the polyfunctional (meth) acrylate compound including the oxyethylene group may be included to give flexibility.
  • the polyfunctional (meth) acrylate-based compound including the oxyethylene group can be used without limitation, those generally used in the art.
  • the polyfunctional (meth) acrylate compound containing the oxyethylene group is trimethylolpropane (EO) 3 tri (meth) acrylate, trimethylol propane (EO) 6 tri (meth) acrylate, trimethylol propane (EO) 9 tri (meth) acrylate, glycerin (EO) 3 tri (meth) acrylate, glycerin (EO) 6 tri (meth) acrylate, glycerin (EO) 9 tri (meth) acrylate, pentaerythritol (EO) 4 Tetra (meth) acrylate, pentaerythritol (EO) 8 tetra (meth) acrylate, pentaerythritol (EO) 12 tetra (meth) acrylate, dipentaerythritol (EO) 6 hexa (
  • the polyfunctional (meth) acrylate-based compound including the oxyethylene group is obtained by addition reaction of ethylene oxide to a polyhydric alcohol to obtain a polyfunctional alcohol having an ethylene glycol group, and condensation of (meth) acrylic acid to the polyfunctional alcohol. It may be prepared by the reaction, but is not limited thereto.
  • the polyfunctional alcohol may be a polyhydric alcohol, and specifically, may be glycerol, trimethylolpropane, pentaerythritol, or dipentaerythritol, but is not limited thereto.
  • the multifunctional (meth) acrylate compound including the oxyethylene group may be represented by the following Formula 5.
  • the hard coating composition includes a polyfunctional (meth) acrylate-based compound including the oxyethylene group, it is possible to provide a hard coating composition capable of producing a hard coating layer having excellent durability and flexibility.
  • the polyfunctional (meth) acrylate compound including the oxyethylene group may be included in an amount of 3 to 10 parts by weight, preferably 5 to 8 parts by weight, based on 100 parts by weight of the total hard coating composition.
  • the mechanical properties, in particular, the hardness may be slightly reduced, and when the above range is exceeded, the shrinkage force is slightly increased, resulting in curling of the film. It is preferable to include within the above range because it may occur, breakage, cracks and the like.
  • the hard coating composition comprises a photoinitiator; solvent; And an additive selected from the group consisting of a leveling agent and a stabilizer; may further include one or more selected from the group consisting of.
  • the photoinitiator is used for photocuring the hard coating composition, and may be applied without limitation as long as it is generally used in the art.
  • the photoinitiator may use a hydrogen decyclic type 2 initiator by coexisting with a type 1 type initiator and a tertiary amine in which radicals are generated by the decomposition of molecules by a difference in chemical structure or molecular binding energy.
  • Type 1 type initiator examples include 4-phenoxydichloroacetphenone, 4-t-butyldichloroacetphenone, 4-t-butyltrichloroacetphenone, diethoxyacetphenone, 2-hydroxy-2-methyl- 1-phenylpropan-1-one, 1- (4-isopropylphenyl) -2-hydroxy-2-methylpropan-1-one, 1- (4-dodecylphenyl) -2-hydroxy-2- Acetphenones such as methylpropan-1-one, 4- (2-hydroxyethoxy) -phenyl (2-hydroxy-2-propyl) ketone, and 1-hydroxycyclohexylphenylketone, benzoin, benzoin Benzoin, such as methyl ether, benzoin ethyl ether, benzyl dimethyl ketal, an acyl phosphine oxide, a titanocene compound, etc. are mentioned.
  • Type 2 type photoinitiator examples include benzophenone, benzoylbenzoic acid, benzoylbenzoic acid methyl ether, 4-phenylbenzophenone, hydroxybenzophenone, 4-benzol-4'-methyldiphenyl sulfide, and 3,3 '.
  • Benzophenones such as -methyl-4-methoxybenzophenone, thioxanthone, 2-chlorothioxanthone, 2-methyl thioxanthone, 2,4-dimethyl thioxanthone and isopropyl thioxanthone Oxanthone etc. are mentioned.
  • the photoinitiator may be used in one kind or in combination of two or more kinds.
  • Type 1 and Type 2 may be used alone or in combination.
  • the photoinitiator is used in an amount capable of sufficiently proceeding photopolymerization, and may be included in an amount of 0.1 to 5 parts by weight, preferably 1 to 3 parts by weight, based on 100 parts by weight of the total hard coating composition, but is not limited thereto.
  • the photoinitiator when included in less than the above range hardening does not proceed sufficiently, it may be difficult to implement the mechanical properties or adhesion of the final obtained coating film, if it exceeds the above range, poor adhesion or cracking phenomenon due to curing shrinkage, Since curling may occur, it is preferable to use within the above range.
  • the solvent may be used without limitation so long as it is known as a solvent of the composition for forming a coating layer in the art that can dissolve or disperse the above-mentioned composition.
  • alcohol type methanol, ethanol, isopropanol, butanol, propylene glycol methoxy alcohol, etc.
  • ketone type methyl ethyl ketone, methyl butyl ketone, methyl isobutyl ketone, diethyl ketone, dipropyl ketone, etc.
  • acetate type Methyl acetate, ethyl acetate, butyl acetate, propylene glycol methoxy acetate, etc.
  • cellosolves methyl cellosolve, ethyl cellosolve, propyl cellosolve, etc.
  • hydrocarbons normal hexane, normal heptane, benzene, toluene, xylene Etc.
  • the said solvent can be used individually or in combination of 2 or more, respectively.
  • the solvent may be included in 5 to 90 parts by weight, preferably 7 to 85 parts by weight based on 100 parts by weight of the total hard coating composition.
  • the solvent is included in the range below the high viscosity may be slightly lower workability, if it exceeds the above range it is difficult to adjust the thickness of the coating film and dry stains may occur appearance defects may be included within the above range Do.
  • the hard coating composition according to the present invention may further include an additive, the additive may include one or more of the group consisting of a leveling agent and a stabilizer, but is not limited thereto, and further includes additives commonly used in the art. It may include.
  • the hard coating composition according to the present invention may further comprise a leveling agent.
  • the leveling agent may be added to give the smoothness and coatability of the coating film when coating the hard coating composition.
  • the leveling agent may be used by selecting a commercially available leveling agent in the form of silicon, a leveling agent in the form of fluorine, an acrylic polymer type, for example, BYK-323, BYK-331, BYK-333, BYK of BYK Chemical Co., Ltd.
  • TEGO Glide 410 TEGO Glide 411, TEGO Glide 415, TEGO Glide 420, TEGO Glide 432, TEGO Glide 435, TEGO Glide 440, TEGO Glide 450, TEGO Glide 455, TEGO Rad 2100, TEGO Rad 2200N, TEGO Rad 2250, TEGO Rad 2300, TEGO Rad 2500, 3M's FC-4430, FC-4432, Shin-Etsu's KY-1203, etc. may be used. Does not.
  • the leveling agent may be used in the range of 0.01 to 0.05 parts by weight based on 100 parts by weight of the total hard coating composition.
  • the leveling agent is included in the range with respect to the hard coating composition has the advantage of maintaining the hardness and flexibility while maximizing the smoothness and coating properties of the coating film.
  • the hard coating composition according to the present invention may further include a UV stabilizer, a heat stabilizer and the like.
  • the ultraviolet stabilizer refers to an additive added to protect the adhesive by blocking or absorbing ultraviolet rays because the surface of the cured coating film is discolored and brittle due to continuous ultraviolet exposure.
  • the UV stabilizers may be classified into absorbents, quenchers, and hindered amine light stabilizers (HALS) according to functional mechanisms, or phenyl salicylates (absorbers) according to chemical structure.
  • HALS hindered amine light stabilizers
  • phenyl salicylates phenyl salicylates
  • Benzophenone Benzophenone, absorbent
  • benzotriazole Benzotriazole, absorbent
  • nickel derivative quencher
  • radical scavenger Radical Scavenger
  • the UV stabilizer that does not significantly change the initial color of the adhesive in the present invention is not particularly limited, and UV stabilizers commonly used in the art can be used.
  • the heat stabilizer is a commercially applicable product, but may be used alone or in combination of polyphenol-based, secondary heat stabilizer, phosphite and lactone, respectively, but is not limited thereto.
  • the UV stabilizer and the heat stabilizer may be used by appropriately adjusting the content at a level that does not affect the UV curability.
  • Hard coating composition according to the present invention is a dendrimer comprising a (meth) acrylate end group; Fluorine-type polyfunctional (meth) acrylate compound containing the urethane group represented by the said Formula (1); And inorganic nanoparticles, and thus have superior flexibility and superior hardness, wear resistance, scratch resistance, and the like, when the above components are used alone.
  • the hard coating composition according to the present invention includes a polymer compound, a photostimulator, an antioxidant, a UV absorber, a thermal polymer inhibitor, and an interface which are commonly used in the art within the range that does not impair the effects of the present invention.
  • Active agents, lubricants, antifouling agents and the like may further be included. At this time, the selection and content control of each additive can be appropriately selected by those skilled in the art.
  • Another aspect of the present invention relates to a hard coat film comprising the cured product of the hard coat composition described above.
  • the hard coating film may be formed by applying the above-described hard coating composition on one side or both sides of the transparent base film and then curing.
  • the hard coat film produced using the hard coat composition according to the present invention exhibits excellent properties in hardness, flexibility, and wear resistance.
  • the base film is not limited as long as it is a transparent polymer film.
  • the "transparent" means that the visible light transmittance is 70% or more or 80% or more. In addition, it may also include the case where all the area is not transparent and opening ratio is 60% or more.
  • the polymer film may be prepared by a film forming method or an extrusion method according to the molecular weight and the film production method, and may be used without limitation as long as it is a commercially available transparent polymer film.
  • adhesion when applied to a crystalline polymer substrate, engineering plastic substrate, difficult to give adhesion after coating, polymer substrate whose surface is changed to hydrophilicity by hydrolysis or saponification, the adhesion can be increased without deterioration of mechanical properties.
  • adhesion when the corona treatment is performed to coat the hard coat layer of the present invention, adhesion may be further increased.
  • the thickness of the base film may be 8 ⁇ 1000 ⁇ m, specifically 40 ⁇ 100 ⁇ m.
  • the strength of the film is high, and thus the workability is excellent, and the phenomenon in which the transparency is lowered can be prevented, and the weight of the hard coat film is advantageous.
  • the coating layer may be prepared using the hard coating composition described above. Specifically, the coating layer may be in a suitable manner such as die coater, air knife, reverse roll, spray, blade, casting, gravure, micro gravure and spin coating.
  • the coating layer may have a thickness of 3 ⁇ m to 200 ⁇ m, specifically 5 ⁇ m to 100 ⁇ m, more specifically 8 ⁇ m to 30 ⁇ m, but is not limited thereto. However, when the thickness of the coating layer satisfies the above range, the hardness of the coating layer may be excellent and flexible, thin, and the hard coating film may hardly be produced.
  • the thickness of the coating layer may refer to the thickness after drying.
  • the hard coating composition After applying the hard coating composition is dried by evaporation of volatiles for 10 seconds to 1 hour, specifically 30 seconds to 10 minutes at a temperature of 30 ⁇ 150 °C. Thereafter, the hard coating composition is cured by irradiating UV light.
  • the irradiation amount of the UV light may be about 0.01 ⁇ 10J / cm 2 , specifically, may be 0.1 ⁇ 2J / cm 2 .
  • the hard coating film may be for a flexible display, and in particular, a display such as an LCD, OLED, LED, FED, or a cover glass such as a touch panel, an electronic paper, or the like of various mobile communication terminals, smartphones or tablet PCs using the same. Or as a functional layer.
  • Still another aspect of the present invention relates to an image display device including the hard coat film described above.
  • the image display device may include a liquid crystal display device, an OLED, a flexible display, and the like, but is not limited thereto.
  • Examples of the image display device may include all image display devices known in the art.
  • Another aspect of the present invention relates to a window of a flexible display device including the hard coat film described above.
  • the hard coating composition prepared according to Examples and Comparative Examples was dried on one surface of an optical polyimide film (Mitsubishi Chemical, 100 ⁇ m, L-3430), and then coated to have a thickness of 10 ⁇ m and dried in an 80 degree oven for 5 minutes. After curing with a light amount of 500mJ in a high pressure mercury lamp to prepare a hard coating film.
  • an optical polyimide film Mitsubishi Chemical, 100 ⁇ m, L-3430
  • Pencil hardness was measured using a pencil hardness tester (PHT, Korea Seokbo Science). Pencils were made using Mitsubishi products, and were carried out five times for each pencil hardness. If there were two or more gases, it was judged as bad and the maximum hardness determined as good was recorded.
  • Kis 0 Good
  • the steel wool tester (WT-LCM100, Korea Protec Co., Ltd.) was used to test wear resistance by reciprocating 10 times under 1 kg / (2 cm ⁇ 2 cm). Steel wool used # 0000.
  • the loads were evaluated by performing 10 reciprocating friction tests using steel wool having a contact area of 3 ⁇ 2.5 cm with a load of 3.75 kgf.
  • Friction coefficient after 10 round trips Value of horizontal and vertical loads during 10 round trips
  • n number of rectangles that do not peel out of the entire rectangle
  • ⁇ height average of four corners is 20 mm or less
  • ⁇ height average of the four corners is greater than 20 mm and less than 50 mm
  • the film After folding in half so that the space
  • the coated film samples cut to a size of 1cm ⁇ 10cm were placed on the iron bars of each diameter (2 ⁇ ⁇ 20 ⁇ ), and the coating layer was turned upward to bend the surface. The smallest diameter that does not occur is indicated.
  • Example 1 Example 2 Example 3 Comparative Example 1 Comparative Example 2 Pencil hardness 3H 3H 3H HB HB Scratch resistance A S S C C Coefficient of friction 0.29 0.26 0.26 0.53 0.51 Adhesion 100/100 100/100 100/100 80/100 70/100 curl ⁇ ⁇ ⁇ ⁇ ⁇ Room temperature flex resistance Good Good Good Bad Bad High temperature, high humidity flex resistance Good Good Good Good Bad Bad Mandorel 3 ⁇ 3 ⁇ 3 ⁇ 16 ⁇ 18 ⁇
  • the hard coating film prepared using the hard coating composition according to the embodiment is excellent in scratch resistance, abrasion resistance, and flex resistance, but hard prepared using the hard coating composition according to the comparative example It can be seen that the coated film is poor in scratch resistance, wear resistance, and flex resistance.

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Abstract

Une composition de revêtement dur selon la présente invention comprend: un dendrimère contenant un groupe terminal (méth)acrylate; un composé (méth)acrylate polyfonctionnel fluoré contenant un groupe uréthane représenté par la formule (1); et des nanoparticules inorganiques.
PCT/KR2017/011966 2017-02-06 2017-10-27 Composition de revêtement dur, et film de revêtement dur utilisant celle-ci WO2018143539A1 (fr)

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KR1020170016181A KR102008320B1 (ko) 2017-02-06 2017-02-06 하드코팅 조성물 및 이로부터 형성되는 하드코팅 필름

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KR102332887B1 (ko) 2019-10-01 2021-11-30 동우 화인켐 주식회사 하드코팅 필름 및 이를 포함하는 화상표시장치
KR102327415B1 (ko) * 2019-10-01 2021-11-17 동우 화인켐 주식회사 하드코팅 필름 및 이를 포함하는 화상표시장치

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JP2006137021A (ja) * 2004-11-10 2006-06-01 Asahi Glass Co Ltd 転写体の製造方法
JP2007290980A (ja) * 2006-04-21 2007-11-08 Shin Etsu Chem Co Ltd 含フッ素（メタ）アクリル酸エステル
WO2016125795A1 (fr) * 2015-02-05 2016-08-11 旭硝子株式会社 Composition de résine photosensible, procédé de production de film de résine, procédé de production d'élément semi-conducteur organique, et polymère contenant du fluor
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JP2007290980A (ja) * 2006-04-21 2007-11-08 Shin Etsu Chem Co Ltd 含フッ素（メタ）アクリル酸エステル
WO2016125795A1 (fr) * 2015-02-05 2016-08-11 旭硝子株式会社 Composition de résine photosensible, procédé de production de film de résine, procédé de production d'élément semi-conducteur organique, et polymère contenant du fluor
KR20170006515A (ko) * 2015-07-08 2017-01-18 동우 화인켐 주식회사 하드코팅 형성용 조성물, 이를 이용한 광학 필름 및 화상 표시 장치

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