KR102316082B1 - Composition for making hard coating layer - Google Patents

Abstract

The present invention relates to a composition for forming a hard coating layer, and more particularly, to an epoxy siloxane resin having a weight average molecular weight of 500 to 30,000 and a polydispersity index (PDI) of 2.0 to 4.0; photoinitiators; And by including a thermosetting agent, it has remarkably improved hardness, it relates to a composition for forming a hard coat layer that can form a hard coat layer with minimized curl due to excellent flexibility.

Description

Composition for forming a hard coating layer {COMPOSITION FOR MAKING HARD COATING LAYER}

The present invention relates to a composition for forming a hard coat layer.

Recently, a thin display device using a flat panel display such as a liquid crystal display or an organic light emitting diode display has received great attention. In particular, these thin display devices are implemented in the form of a touch screen panel, and are characterized by portability to various wearable devices as well as smart phones and tablet PCs. It is widely used in various smart devices.

Such portable touch screen panel-based display devices have a window cover for display protection on the display panel to protect the display panel from scratches or external impact, and in most cases, tempered glass for display is used as the window cover. Tempered glass for display is thinner than general glass, but it has high strength and is strong against scratches.

However, tempered glass has the disadvantage that it is not suitable for reducing the weight of portable devices because it is heavy in weight, and it is difficult to implement unbreakable properties because it is vulnerable to external shocks, and it is not bent over a certain level and is bendable. It is not suitable as a flexible display material having a foldable function.

Recently, various studies have been conducted on optical plastic covers that have strength or scratch resistance corresponding to tempered glass while securing flexibility and impact resistance. In general, the optical transparent plastic cover material that has more flexibility than tempered glass is polyethylene terephthalate (PET), polyethersulfone (PES), polyethylene naphthalate (PEN), polyacrylate (PAR), polycarbonate (PC). , polyimide (PI), and polyaramid (PA). However, in the case of these polymer plastic substrates, compared to tempered glass used as a window cover for display protection, not only exhibit insufficient physical properties in terms of hardness and scratch resistance, but also insufficient impact resistance. Therefore, various attempts are being made to supplement the physical properties required by coating the composite resin composition on these plastic substrates.

In the case of a general hard coating, a composition consisting of a resin containing a photocurable functional group such as (metha)acrylate or epoxy, a curing agent or a curing catalyst and other additives is used, and in particular, In the case of a composite resin, it can be used as a display protection window with improved hardness and scratch resistance by coating it on an optical plastic base film.

However, in the case of general (meth)acrylate or epoxy high-functional group photocurable composite resin, it is difficult to realize high hardness corresponding to tempered glass, and curl phenomenon due to shrinkage occurs greatly during curing, and flexibility is also There is a disadvantage in that it is not sufficient as a protective window substrate for application to a flexible display.

Korean Patent Application Laid-Open No. 2013-74167 discloses a plastic substrate.

Korea Patent Publication No. 2013-74167

An object of the present invention is to provide a composition capable of forming a hard coating layer having significantly improved hardness.

An object of the present invention is to provide a composition capable of forming a hard coating layer having excellent flexibility.

An object of the present invention is to provide a hard coat film having the hard coat layer.

1. an epoxy siloxane resin having a weight average molecular weight of 500 to 30,000 and a polydispersity index (PDI) of 2.0 to 4.0; photoinitiators; And a composition for forming a hard coat layer comprising a thermosetting agent.

2. The composition of the above 1, wherein the siloxane resin has a weight average molecular weight of 1,000 to 20,000.

3. The composition of the above 1, wherein the siloxane resin has a weight average molecular weight of 5,000 to 15,000.

4. The composition of the above 1, wherein the siloxane resin has an epoxy group equivalent of 3.0 to 6.3 mmol/g.

5. The composition for forming a hard coating layer according to the above 1, wherein the siloxane resin is polymerized by including a monomer having an aryl group in an amount of 10% by weight or less based on the total weight of the monomer.

6. The composition for forming a hard coat layer according to the above 1, wherein the siloxane resin has a UV absorption spectrum peak having a maximum absorbance at a wavelength of 200 to 250 nm.

7. The composition for forming a hard coating layer according to 1 above, wherein the thermosetting agent is at least one selected from the group consisting of amine-based, imidazole-based, acid anhydride-based, and amide-based thermal curing agents.

8. The composition for forming a hard coat layer according to the above 1, wherein the thermosetting agent is at least one acid anhydride-based thermosetting agent selected from the group consisting of the following formulas (1) to (15).

(Wherein, n is an integer of 0 to 5, X is an oxygen atom or a methylene group, Ra, Rb, Rc and Rd are each independently a hydrogen atom or an alkyl group having 1 to 10 carbon atoms, and Rs is a carbon number 1 to 20 of an alkylene group, an alkenylene group having 2 to 20 carbon atoms, or an arylene group having 6 to 18 carbon atoms).

9. The composition of the above 1, wherein the thermosetting agent is included in an amount of 5 to 30 parts by weight based on 100 parts by weight of the siloxane resin.

10. A hard coating film comprising a substrate having a hard coating layer formed of the composition for forming a hard coating layer of any one of the above 1 to 9 on at least one surface.

11. The hard coating film of the above 10, wherein the rate of change of the chromaticity b value before and after standing for 1,000 hours at 85° C. and 90% relative humidity condition of the hard coating layer is within 5%.

12. An image display device having the hard coating film of 10 above.

The composition of the present invention can form a hard coating layer having significantly improved hardness.

The composition of the present invention can form a hard coating layer with minimized curl due to excellent flexibility. Accordingly, the hard coating film having a hard coating layer of the present invention can secure excellent flexibility without a separate curl suppression layer.

1 is a schematic cross-sectional view of a hard coat film having a hard coat layer formed of the composition for forming a hard coat layer of the present invention.
Figure 2 schematically shows one embodiment of performing a bending test on a hard coating film having a hard coating layer formed of the composition for forming a hard coating layer of the present invention.
Figure 3 schematically shows one embodiment of performing a bending test on a hard coating film having a hard coating layer formed of the composition for forming a hard coating layer of the present invention.

The present invention relates to an epoxy siloxane resin having a weight average molecular weight of 500 to 30,000 and a polydispersity index (PDI) of 2.0 to 4.0; photoinitiators; And by including a thermosetting agent, it has remarkably improved hardness, and relates to a composition for forming a hard coat layer that can form a hard coat layer with minimized curl due to excellent flexibility.

Hereinafter, the present invention will be described in detail.

<Composition for forming a hard coat layer>

The composition for forming a hard coat layer of the present invention includes an epoxy siloxane resin, a photoinitiator, and a thermosetting agent.

As used herein, the epoxy siloxane resin refers to a siloxane resin having an epoxy group, and the epoxy group may be an alicyclic epoxy group, an aliphatic epoxy group, an aromatic epoxy group, or a mixture thereof.

The epoxy siloxane resin according to the present invention has a weight average molecular weight of 500 to 30,000, preferably 1,000 to 20,000, and more preferably 5,000 to 15,000 in terms of securing high hardness and fairness at the same time.

The polydispersity index (PDI) of the epoxy siloxane resin is 2.0 to 4.0. If the polydispersity index is less than 2.0, it is difficult to simultaneously satisfy both the hardness and ductility of the hard coating layer, and if it exceeds 4.0, the physical properties related to ductility are overexpressed.

The composition for forming a hard coat layer of the present invention can significantly improve hardness by using an epoxy siloxane resin having a weight average molecular weight and a polydispersity index in the specific range. In addition, flexibility is remarkably improved, and bending deformation can be suppressed.

The epoxy group equivalent of the epoxy siloxane resin is not particularly limited, and may be, for example, 3.0 to 6.3 mmol/g. When the epoxy group equivalent is within the above range, it is possible to significantly improve hardness by forming dense crosslinking during polymerization, and also suppress yellowing, which will be described later.

The epoxy siloxane resin according to the present invention can be prepared through hydrolysis and condensation reaction between an alkoxy silane having an epoxy group alone or an alkoxy silane having an epoxy group and a heterogeneous alkoxy silane in the presence of water.

Schemes 1 to 3 below schematically show hydrolysis and condensation reactions of alkoxysilanes in the presence of water and a catalyst.

[Scheme 1]

[Scheme 2]

[Scheme 3]

In Schemes 1 to 3, R is a straight-chain or branched alkyl group having 1 to 7 carbon atoms, R' is a straight-chain or branched-chain alkyl group having 1 to 20 carbon atoms including an epoxy group, a cycloalkyl group having 3 to 8 carbon atoms, and carbon number 3-20 alkenyl group, C2-20 alkynyl group, C6-20 aryl group, acrylic group, methacryl group, halogen group, amino group, mercapto group, ether group, ester group, carbonyl group, carboxyl group, vinyl group, It may include at least one functional group selected from the group consisting of a nitro group, a sulfone group, and an alkyd group.

Scheme 1 above shows that the alkoxy group of the alkoxy silane as a starting material is hydrolyzed by water to form a hydroxyl group. As shown in Scheme 2 or Scheme 3, the hydroxyl group formed through this forms a siloxane bond through a condensation reaction between the hydroxyl groups or alkoxy groups of other silanes. Therefore, the weight average molecular weight and molecular weight distribution (PDI) of the finally formed siloxane compound can be controlled by controlling the reaction rate, and the reaction temperature, the amount, type, and solvent of the catalyst can be major factors.

A catalyst is used to prepare an epoxy siloxane resin having a weight average molecular weight of 500 to 30,000 and a polydispersity index of 2.0 to 4.0 using the above reaction formula. Examples of the usable catalyst include acid catalysts such as hydrochloric acid, acetic acid, hydrogen fluoride, nitric acid, sulfuric acid chlorosulfonic acid, iodic acid, and phyllophosphoric acid; base catalysts such as ammonia, potassium hydroxide, sodium hydroxide, barium hydroxide, imidazole, n-butylamine, di-n-butylamine, tri-n-butylamine, ammonium perchlorate, and tetramethyl-ammonium hydroxide; and ion exchange resins such as Amberite IRA-400 and IRA-67, and may also be selected from the group consisting of combinations thereof.

The amount of the catalyst is not particularly limited, but in the case of an acid catalyst and a base catalyst, about 0.0001 to about 0.01 parts by weight may be added based on about 100 parts by weight of the alkoxy silane, and in the case of an ion exchange resin, about 1 to about 100 parts by weight of the alkoxy silane to about 10 parts by weight may be added, but may not be limited thereto.

The hydrolysis and condensation reaction may be carried out by stirring at room temperature for about 12 hours to about 7 days, but in order to promote the reaction, stirring may be performed at about 60° C. to about 100° C. for about 2 hours to about 72 hours. , which may not be limited thereto.

As can be seen in Schemes 1 to 3, when the reaction occurs, alcohol and water, which are by-products, are generated. By removing these, a reverse reaction can be reduced and a forward reaction can be induced, thereby controlling the reaction rate. In addition, when the reaction is completed, alcohol and water remaining in the siloxane resin may be removed by applying a condition of about 60° C. to about 100° C. under reduced pressure for about 10 minutes to about 60 minutes, but may not be limited thereto.

An alkoxy silane having an epoxy group used in the preparation of an epoxy siloxane resin according to an embodiment of the present invention may be exemplified by the following Chemical Formula 1:

[Formula 1]

R ¹ _n Si(OR ² ) _4-n

(Wherein, R ¹ is a linear or branched alkyl group having 1 to 6 carbon atoms substituted with an epoxycycloalkyl group having 3 to 6 carbon atoms or an oxiranyl group, and may be interrupted by oxygen,

R ² is a straight-chain or branched alkyl group having 1 to 7 carbon atoms,

n is an integer from 1 to 3).

The alkoxysilane represented by Formula 1 is not particularly limited, and for example, 2-(3,4-epoxycyclohexyl)ethyltrimethoxysilane, 2-(3,4-epoxycyclohexyl)ethyltriethoxysilane , 3-glycidoxypropyl trimethoxysilane, and the like. These can be used individually or in mixture of 2 or more types.

In one embodiment of the present application, the epoxy siloxane resin may be prepared solely by an alkoxysilane having an epoxy group, but also may be prepared through hydrolysis and condensation reaction between an alkoxysilane having an epoxy group and a heterogeneous alkoxysilane. may not be limited.

The heterogeneous alkoxy silane may be used by selecting one or more types from the alkoxy silanes represented by the following formula (2):

[Formula 2]

R ³ _m Si(OR ⁴ ) _4-m ;

(wherein, R ³ is an alkyl group having 1 to 20 carbon atoms, a cycloalkyl group having 3 to 8 carbon atoms, an alkenyl group having 3 to 20 carbon atoms, an alkynyl group having 2 to 20 carbon atoms, an aryl group having 6 to 20 carbon atoms, acryl group, methacryl group It may include at least one functional group selected from the group consisting of a group, a halogen group, an amino group, a mercapto group, an ether group, an ester group, a carbonyl group, a carboxyl group, a vinyl group, a nitro group, a sulfone group and an alkyd group,

R ⁴ is a straight-chain or branched alkyl group having 1 to 7 carbon atoms, and m is an integer of 0 to 3).

The alkoxysilane represented by Formula 2 is not particularly limited, and for example, tetramethoxysilane, tetraethoxysilane, methyltrimethoxysilane, methyltriethoxysilane, methyltripropoxysilane, dimethyldimethoxy Silane, dimethyldiethoxysilane, phenyltrimethoxysilane, phenyltriethoxysilane, diphenyldimethoxysilane, diphenyldiethoxysilane, triphenylmethoxysilane, triphenylethoxysilane, ethyltrie Toxysilane, propylethyltrimethoxysilane, vinyltrimethoxysilane, vinyltriethoxysilane, vinyltripropoxysilane, N-(3-acryloxy-2-hydroxypropyl)-3-aminopropyltrimethoxy silane, N-(3-acryloxy-2-hydroxypropyl)-3-aminopropyltriethoxysilane, N-(3-acryloxy-2-hydroxypropyl)-3-aminopropyltripropoxysilane, 3-acryloxypropylmethylbis(trimethoxy)silane, 3-acryloxypropyltrimethoxysilane, 3-acryloxypropyltriethoxysilane, 3-acryloxypropyltripropoxysilane, 3-(meth)acryl Oxypropyltrimethoxysilane, 3-(meth)acryloxypropyltriethoxysilane, 3-(meth)acryloxypropyltripropoxysilane, N-(aminoethyl-3-aminopropyl)trimethoxysilane, N -(2-Aminoethyl-3-aminopropyl)triethoxysilane, 3-aminopropyltrimethoxysilane, 3-aminopropyltriethoxysilane, chloropropyltrimethoxysilane, chloropropyltriethoxysilane, hepta Decafluordecyltrimethoxysilane etc. are mentioned. These can be used individually or in mixture of 2 or more types.

Preferably, the epoxy siloxane resin according to the present invention may be polymerized by including a small amount of a monomer having an aryl group. For example, the monomer having an aryl group may be polymerized by including 10% by weight or less of the total weight of the monomer. If the content of the monomer having an aryl group is more than 10% by weight based on the total weight of the monomer, yellowing of the hard coating layer may occur.

The epoxy siloxane resin according to the present invention may be polymerized without including a monomer having an aryl group in a small amount, and most preferably, a monomer having an aryl group in order to suppress yellowing.

In addition, the epoxy siloxane resin may have a UV absorption spectrum peak exhibiting a maximum absorbance at a wavelength of 200 to 250 nm. When the maximum absorbance is shown at the above wavelength, yellowing of the hard coating layer prepared with the composition of the present invention can be minimized.

As the photoinitiator, a photocationic initiator capable of initiating polymerization of the epoxy siloxane resin and the epoxy-based monomer may be used.

The photocationic initiator may be, for example, an onium salt and/or an organometallic salt, but is not limited thereto. For example, diaryliodonium salts, triarylsulfonium salts, aryldiazonium salts, iron-arene complexes and the like can be used. These can be used individually or in mixture of 2 or more types.

The content of the photoinitiator is not particularly limited, and for example, may be included in an amount of 1 to 15 parts by weight based on 100 parts by weight of the epoxy siloxane resin. When the content of the photoinitiator is within the above range, it is possible to maintain excellent curing efficiency of the composition and prevent deterioration of physical properties due to residual components after curing.

The thermosetting agent is a component that allows the hard coating layer prepared from the composition of the present invention to have superior hardness and flexural properties.

The thermosetting agent may include an amine-based, imidazole-based, acid anhydride-based, amide-based thermal curing agent, and the like, and more preferably an acid anhydride-based thermal curing agent in terms of preventing discoloration and implementing high hardness. These can be used individually or in mixture of 2 or more types.

Specific examples of the amine-based thermosetting agent include piperidine, N,N-dimethylpiperazine, triethylenediamine, 2,4,6-tris(dimethylaminomethyl)phenol, benzyldimethylamine, and 2-(dimethylaminomethyl)phenol. , diethylenetriamine, triethylenetetramine, tetraethylenepentamine, diethylaminopropylamine, N-aminoethylpiperazine, di(1-methyl-2-aminocyclohexyl)methane, mensendiamine, isophoronediamine, and diaminodicyclohexylmethane, 1,3-diaminomethylcyclohexane, xylenediamine, metaphenylenediamine, diaminodiphenylmethane and diaminodiphenylsulfone.

Specific examples of the imidazole-based thermosetting agent include 2-methylimidazole, 2-ethyl-4-methylimidazole, ethylimidazole, isopropylimidazole, 2,4-dimethylimidazole, phenyl Midazole, undecylimidazole, heptadecylimidazole, 2-phenyl-4-methylimidazole, 1-cyanoethyl-2-undecylimidazolium trimellitate and epoxyimidazole adduct ) and the like.

Specific examples of the acid anhydride-based thermosetting agent include phthalic anhydride, trimellitic anhydride, pyromellitic anhydride, benzophenone tetracarboxylic acid anhydride, ethylene glycol bisrimellitate, glycerol tristrimellitate, maleic anhydride, tetrahydrophthalic anhydride , methyltetrahydrophthalic anhydride, endomethylenetetrahydrophthalic anhydride, methylendomethylenetetrahydrophthalic anhydride, methylbutenyltetrahydrophthalic anhydride, dodecenylsuccinic anhydride, hexahydrophthalic anhydride, methylhexahydrophthalic anhydride, succinic anhydride, methyl Cyclohexene dicarboxylic acid anhydride, chlorendic anhydride nadic anhydride, glutaric anhydride, methylnadic anhydride, dichlorosuccinic anhydride, benzophenone tetracarboxylic anhydride, etc. are mentioned.

Among the acid anhydride-based thermosetting agents, in particular, thermosetting agents represented by the following formulas (1) to (15) are preferable. These can be used individually or in mixture of 2 or more types.

(Wherein, n is an integer of 0 to 5, X is an oxygen atom or a methylene group, Ra, Rb, Rc and Rd are each independently a hydrogen atom or an alkyl group having 1 to 10 carbon atoms, and Rs is a carbon number 1 to 20 of an alkylene group, an alkenylene group having 2 to 20 carbon atoms, or an arylene group having 6 to 18 carbon atoms).

Specific examples of the amide-based thermosetting agent include sulfanylamide, dicyandiamide, and polyamide.

The content of the thermosetting agent is not particularly limited, and for example, may be included in an amount of 5 to 30 parts by weight based on 100 parts by weight of the epoxy siloxane resin. When the content of the thermosetting agent is within the above range, the curing efficiency of the composition may be further improved to form a hard coating layer having excellent hardness.

The composition for forming a hard coat layer of the present invention further comprises a solvent.

The solvent according to the present invention is not particularly limited, and solvents known in the art can be used, for example, alcohol-based (methanol, ethanol, isopropanol, butanol, methyl cellulose, ethyl sol-sorb, etc.), ketone-based (methyl Ethyl ketone, methyl butyl ketone, methyl isobutyl ketone, diethyl ketone, dipropyl ketone, cyclohexanone, etc.), hexane type (hexane, heptane, octane, etc.), benzene type (benzene, toluene, xylene, etc.) can be used These can be used individually or in mixture of 2 or more types.

The content of the solvent according to the present invention is not particularly limited, and for example, may be included in an amount of 10 to 80 parts by weight based on 100 parts by weight of the epoxy siloxane resin. If the content is less than 10 parts by weight, the viscosity is high and workability is lowered, and if it exceeds 80 parts by weight, it is difficult to control the thickness of the coating film during thick film coating operation. This can fall.

If necessary, the composition for forming a hard coat layer of the present invention may further include an inorganic filler to improve hardness.

The inorganic filler is not particularly limited, and examples thereof include metal oxides such as silica, alumina, and titanium oxide; hydroxides such as aluminum hydroxide, magnesium hydroxide, and potassium hydroxide; metal particles such as gold, silver, copper, nickel, and alloys thereof; Electroconductive particles, such as carbon, a carbon nanotube, and fullerene; glass; ceramic; and the like, and preferably silica. These can be used individually or in mixture of 2 or more types.

The particle diameter of the inorganic filler is not particularly limited, and for example, the average particle diameter may be 1 to 100 nm. If the average particle diameter is less than 1 nm, the effect of improving the hardness is insignificant, and if it exceeds 100 nm, it may act as a foreign material of the hard coating layer. Preferably, the average particle diameter may be 10 to 30 nm.

The content of the inorganic filler according to the present invention is not particularly limited, and for example, may be included in an amount of 0.1 to 5 parts by weight based on 100 parts by weight of the epoxy siloxane resin. If the content is less than 0.1 parts by weight, the effect of improving the hardness is insignificant, and if it is more than 5 parts by weight, the coating property may be lowered by increasing the viscosity.

If necessary, the composition for forming a hard coat layer of the present invention may further include a lubricant to improve winding efficiency, blocking resistance, abrasion resistance, and scratch resistance.

The type of lubricant according to the present invention is not particularly limited, and examples thereof include waxes such as polyethylene wax, paraffin wax, synthetic wax or montan wax; synthetic resins such as silicone-based resins and fluorine-based resins; and the like. These can be used individually or in mixture of 2 or more types.

The amount of the lubricant according to the present invention is not particularly limited, and for example, may be included in an amount of 0.1 to 5 parts by weight based on 100 parts by weight of the epoxy siloxane resin. When the content is within the above range, while imparting excellent blocking resistance, friction resistance and scratch resistance, the transparency can also be excellently maintained.

In addition, if necessary, additives such as antioxidants, UV absorbers, light stabilizers, thermal polymerization inhibitors, leveling agents, surfactants, lubricants, and antifouling agents may be further included.

<Hard coating film>

In addition, the present invention provides a hard coating film 100 comprising a substrate 110 having a hard coating layer 120 formed of the composition for forming a hard coating layer on at least one surface.

The substrate 110 according to the present invention preferably has excellent transparency, mechanical strength, thermal stability, moisture shielding property, isotropy, and the like, for example, a polyester-based resin such as polyethylene terephthalate, polyethylene isophthalate, and polybutylene terephthalate. ; Cellulose resins, such as a diacetyl cellulose and a triacetyl cellulose; polycarbonate-based resin; acrylic resins such as polymethyl (meth)acrylate and polyethyl (meth)acrylate; styrenic resins such as polystyrene acrylonitrile-styrene copolymer; polyolefin-based resins such as polyethylene, polypropylene, polyolefin-based resins having a cyclo-based or norbornene structure, and ethylenepropylene copolymers; polyimide-based resin; polyaramid-based resin; polyether sulfone-based resin; It may be a substrate made of a sulfone-based resin or the like. These resins can be used individually or in mixture of 2 or more types.

The thickness of the substrate 110 is not particularly limited, and may be, for example, 10 to 250 μm.

The hard coating layer 120 is formed by applying and curing the composition for forming the hard coating layer, and the application is performed by a known method such as a die coater, air knife, reverse roll, spray, blade, casting, gravure, spin coating, etc. can be

In the case of curing, the method is not particularly limited, and for example, photocuring or thermal curing may be performed alone, or thermal curing after photocuring, photocuring after thermal curing, or the like may be used.

The thickness of the hard coating layer 120 is not particularly limited, and may be, for example, 10 to 100 μm. When the thickness is within the above range, the curling phenomenon hardly occurs and the hard coating layer 120 having excellent hardness can be obtained.

The hard coating layer 120 according to the present invention is formed of the composition for forming the hard coating layer and has significantly improved hardness. The hardness may vary depending on the content, type, etc. of the individual composition, but the pencil hardness may be 5H or more, and may be 9H or more at the maximum when each of the above-described compositions is used in combination in a desired amount.

In addition, the flexibility is remarkably improved, and the bending deformation is very small.

In addition, even when exposed to high temperature, high humidity conditions for a long time, it is possible to minimize the occurrence of yellowing. For example, the rate of change of the chromaticity b value before and after standing for 1,000 hours in a moist heat resistant condition of 85° C. and 90% relative humidity may be within 5%.

The hard coating film 100 of the present invention has a very high surface hardness and at the same time has a hard coating layer 120 having excellent flexibility, and is lighter than tempered glass and has excellent impact resistance. It can be used preferably.

In addition, the present invention provides an image display device having the hard coating film (100).

The hard coating film 100 may be used as an outermost window substrate of an image display device, and the image display device is a conventional liquid crystal display device, an electroluminescence display device, a plasma display device, a field emission display device, etc. Various image display devices. can

Hereinafter, examples will be given to describe the present invention in detail.

manufacturing example One

2-(3,4-epoxycyclohexyl)ethyltrimethoxysilane (ECTMS, TCI) and water (H2O, Sigma-Aldrich) were mixed in a ratio of 24.64g: 2.70g (0.1mol: 0.15mol) It was placed in a 250 mL 2 neck flask. Then, 0.1 mL of tetramethylammonium hydroxide was added to the mixture and 100 mL of methyl ethyl ketone was added, followed by stirring at 60° C. for 36 hours. Then, it was filtered using a 0.45 μm Teflon filter to obtain an alicyclic epoxy siloxane resin. The molecular weight of the alicyclic epoxy siloxane resin was measured using gel permeation chromatography (GPC).

manufacturing example 2

2-(3,4-epoxycyclohexyl)ethyltrimethoxysilane (ECTMS, TCI) and water (H ₂ O, Sigma-Aldrich) in a ratio of 24.64g: 2.70g (0.1mol: 0.15mol) The mixture was put into a 250 mL 2 neck flask. Then, 0.1 mL of tetramethylammonium hydroxide, a catalyst and 50 mL of methyl ethyl ketone were added to the mixture, and the mixture was stirred at 70° C. for 24 hours. Then, it was filtered using a 0.45㎛ Teflon filter (Teflon filter) to obtain an alicyclic epoxy siloxane resin. The molecular weight of the alicyclic epoxy siloxane resin was measured using gel permeation chromatography (GPC).

manufacturing example 3

2-(3,4-epoxycyclohexyl)ethyltrimethoxysilane (ECTMS, TCI) and water (H2O, Sigma-Aldrich) were mixed in a ratio of 24.64g: 2.70g (0.1mol: 0.15mol) It was placed in a 100 mL 2 neck flask. Then, 0.1 mL of tetramethylammonium hydroxide was added to the mixture as a catalyst, and the mixture was stirred at 80° C. for 24 hours. Then, filtration using a 0.45㎛ Teflon filter (Teflon filter) to obtain an alicyclic epoxy siloxane resin. The molecular weight of the alicyclic epoxy siloxane resin was measured using gel permeation chromatography (GPC).

manufacturing example 4

2-(3,4-epoxycyclohexyl)ethyltrimethoxysilane (ECTMS, TCI) and water (H2O, Sigma-Aldrich) were mixed in a ratio of 24.64g: 2.70g (0.1mol: 0.15mol) It was placed in a 100 mL 2 neck flask. Then, 0.1 mL of tetramethylammonium hydroxide was added to the mixture and 100 mL of methyl ethyl ketone was added, followed by stirring at 60° C. for 36 hours. Then, filtration using a 0.45㎛ Teflon filter (Teflon filter) to obtain an alicyclic epoxy siloxane resin. The molecular weight of the alicyclic epoxy siloxane resin was measured using gel permeation chromatography (GPC).

manufacturing example 5

2-(3,4-epoxycyclohexyl)ethyltrimethoxysilane (ECTMS, TCI) and water (H2O, Sigma-Aldrich) were mixed in a ratio of 24.64g: 2.70g (0.1mol: 0.15mol) It was placed in a 100 mL 2 neck flask. Then, 1.0 mL of tetramethylammonium hydroxide was added to the mixture as a catalyst, and the mixture was stirred at 70° C. for 36 hours. Then, filtration using a 0.45㎛ Teflon filter (Teflon filter) to obtain an alicyclic epoxy siloxane resin. The molecular weight of the alicyclic epoxy siloxane resin was measured using gel permeation chromatography (GPC).

manufacturing example 6

2-(3,4-epoxycyclohexyl)ethyltrimethoxysilane (ECTMS, TCI) and water (H2O, Sigma-Aldrich) were mixed in a ratio of 24.64g: 2.70g (0.1mol: 0.15mol) It was placed in a 100 mL 2 neck flask. Then, 0.2 mL of tetramethylammonium hydroxide was added to the mixture, and 50 mL of methyl ethyl ketone was added, followed by stirring at 60° C. for 36 hours. Then, filtration using a 0.45㎛ Teflon filter (Teflon filter) to obtain an alicyclic epoxy siloxane resin. The molecular weight of the alicyclic epoxy siloxane resin was measured using gel permeation chromatography (GPC).

manufacturing example 7

2-(3,4-epoxycyclohexyl)ethyltrimethoxysilane (ECTMS, TCI), diphenylsilanediol (DPSD, TCI), and water (H ₂ O, Sigma-Aldrich) 24.64g: 2.164 g: 2.7 g (0.1 mol: 0.01 mol: 0.15 mol) was mixed in a ratio and put into a 100 mL 2 neck flask. Then, 0.2 mL of tetramethylammonium hydroxide was added to the mixture, and 50 mL of methyl ethyl ketone was added, followed by stirring at 60° C. for 36 hours. Then, filtration using a 0.45㎛ Teflon filter (Teflon filter) to obtain an alicyclic epoxy siloxane resin. The molecular weight of the alicyclic epoxy siloxane resin was measured using gel permeation chromatography (GPC).

manufacturing example 8

2-(3,4-epoxycyclohexyl)ethyltrimethoxysilane (ECTMS, TCI), diphenylsilanediol (DPSD, TCI), and water (H ₂ O, Sigma-Aldrich) 24.64g: 3.246 g: 2.7 g (0.1 mol: 0.015 mol: 0.15 mol) was mixed in a ratio and put into a 100 mL 2 neck flask. Then, 0.2 mL of tetramethylammonium hydroxide was added to the mixture, and 50 mL of methyl ethyl ketone was added, followed by stirring at 60° C. for 36 hours. Then, filtration using a 0.45㎛ Teflon filter (Teflon filter) to obtain an alicyclic epoxy siloxane resin. The molecular weight of the alicyclic epoxy siloxane resin was measured using gel permeation chromatography (GPC).

manufacturing example 9

2-(3,4-epoxycyclohexyl)ethyltrimethoxysilane (ECTMS, TCI): 24.64g of diphenylsilanediol (DPSD, TCI), water (H ₂ O, Sigma-Aldrich): 10.82 g: 2.7 g (0.1 mol: 0.05 mol: 0.15 mol) was mixed in a ratio and put in a 100 mL 2 neck flask. Then, 0.2 mL of tetramethylammonium hydroxide was added to the mixture, and 50 mL of methyl ethyl ketone was added, followed by stirring at 60° C. for 36 hours. Then, filtration using a 0.45㎛ Teflon filter (Teflon filter) to obtain an alicyclic epoxy siloxane resin. The molecular weight of the alicyclic epoxy siloxane resin was measured using gel permeation chromatography (GPC).

manufacturing example 10

2-(3,4-epoxycyclohexyl)ethyltrimethoxysilane (ECTMS, TCI) and water (H2O, Sigma-Aldrich) were mixed in a ratio of 24.64g: 2.70g (0.1mol: 0.15mol) It was placed in a 100 mL 2 neck flask. Then, 0.05 mL of tetramethylammonium hydroxide and 50 mL of methyl ethyl ketone were added to the mixture, followed by stirring at 70° C. for 36 hours. Then, filtration using a 0.45㎛ Teflon filter (Teflon filter) to obtain an alicyclic epoxy siloxane resin. The molecular weight of the alicyclic epoxy siloxane resin was measured using gel permeation chromatography (GPC).

manufacturing example 11

2-(3,4-epoxycyclohexyl)ethyltrimethoxysilane (ECTMS, TCI) and water (H2O, Sigma-Aldrich) were mixed in a ratio of 24.64g: 2.70g (0.1mol: 0.15mol) It was placed in a 100 mL 2 neck flask. Then, 0.5 mL of tetramethylammonium hydroxide, a catalyst and 50 mL of methyl ethyl ketone were added to the mixture, and the mixture was stirred at 70° C. for 24 hours. Then, filtration using a 0.45㎛ Teflon filter (Teflon filter) to obtain an alicyclic epoxy siloxane resin. The molecular weight of the alicyclic epoxy siloxane resin was measured using gel permeation chromatography (GPC).

manufacturing example 12

2-(3,4-epoxycyclohexyl)ethyltrimethoxysilane (ECTMS, TCI), phenyltrimethoxysilane (PTMS, Sigma-Aldrich), and water (H ₂ O, Sigma-Aldrich) were mixed with 11.09 g: 13.22 g: 2.70 g (0.045 mol: 0.055 mol: 0.15 mol) was mixed in the ratio of the mixture was put into a 250 mL 2 neck flask. Then, 0.1 mL of tetramethylammonium hydroxide was added to the mixture, and 50 mL of methyl ethyl ketone was added, followed by stirring at 80° C. for 24 hours. Then, it was filtered using a 0.45 μm Teflon filter to obtain an alicyclic epoxy siloxane resin. The molecular weight of the alicyclic epoxy siloxane resin was measured using gel permeation chromatography (GPC).

division Mn Mw PDI (Mw/Mn) Epoxy group equivalent (mmol/g) Maximum UV absorption wavelength (nm) Preparation Example 1 650 1980 3.05 6.3 220nm Preparation 2 2300 5500 2.39 6.3 217nm Preparation 3 3645 11745 3.22 6.3 220nm Preparation 4 972 2430 2.50 6.3 225nm Preparation 5 4210 8700 2.07 6.3 223nm Preparation 6 1740 6800 3.91 6.3 220nm Preparation 7 1771 5500 3.11 5.2 245nm Preparation 8 3560 8560 2.40 4.8 270nm Preparation 9 2590 10500 4.05 6.3 227nm Preparation 10 2804 5206 1.86 6.3 224nm Preparation 11 1210 5320 4.40 6.3 220nm Preparation 12 1700 5000 2.94 2.84 219nm

Example and comparative example

A composition for forming a hard coat layer having the composition and content shown in Table 2 was prepared.

division Siloxane resin photoinitiator thermosetting agent menstruum ingredient parts by weight ingredient parts by weight ingredient parts by weight ingredient parts by weight Example 1 Preparation Example 1 50 A 5 B-1 10 C 35 Example 2 Preparation 2 50 A 5 B-1 10 C 35 Example 3 Preparation 3 50 A 5 B-1 10 C 35 Example 4 Preparation 4 50 A 5 B-1 10 C 35 Example 5 Preparation 5 50 A 5 B-1 10 C 35 Example 6 Preparation 6 50 A 5 B-1 10 C 35 Example 7 Preparation 7 50 A 5 B-1 10 C 35 Example 8 Preparation 2 50 A 5 B-1 15 C 35 Example 9 Preparation 2 50 A 5 B-1 5 C 35 Example 10 Preparation 2 50 A 5 B-2 10 C 35 Example 11 Preparation 2 50 A 5 B-3 10 C 35 Example 12 Preparation 2 50 A 5 B-4 10 C 35 Example 13 Preparation 8 50 A 5 B-1 10 C 35 Example 14 Preparation 12 50 A 5 B-1 10 C 35 Comparative Example 1 Preparation 10 50 A 5 B-1 10 C 35 Comparative Example 2 Preparation 11 50 A 5 B-1 10 C 35 Comparative Example 3 Preparation 2 50 A 5 - - C 35 Comparative Example 4 Preparation 3 50 A 5 - - C 35 Comparative Example 5 Preparation 4 50 A 5 - - C 35 Comparative Example 6 Preparation 9 50 A 5 B-1 10 C 35 A: (4-methylphenyl) [4- (2-methylpropyl) phenyl] iodonium hexafluorophosphate
B-1: methyl-5-norbornene-2,3-dicarboxylic anhydride
B-2: tetraethylenetetramine
B-3: 2-ethylimidazole
B-4: dicyandiamide
C: methyl ethyl ketone

Experimental example

The composition for forming the hard coating layer of Examples and Comparative Examples was applied to a 125um PET film (SKC) using a Meyer bar, cured at 100°C for 10 minutes, and UV-irradiated at 1J/cm2 using a high-pressure mercury lamp, followed by UV irradiation at 150°C for 10 minutes. After curing for minutes, a hard coating layer having a thickness of 50 μm was obtained.

(1) Measurement of pencil hardness

The hardness of the hard coating layer was measured using a pencil hardness meter according to JIS K5600.

(2) flexibility evaluation

As shown in FIG. 2, the substrate prepared in Experimental Example (1) was wrapped around 180° so that the hard coating layer was outside on the inside of the cylinder of the _{bottom radius R 1 as shown in FIG. The minimum R 1 in} which no bending deformation was observed was recorded.

And, as shown in FIG. 3 , it was wound at 180° so that the hard coating layer came to the outside of the cylinder of the _{base radius R 2 , and then returned to the original position, and then the minimum R 2 in} which no bending deformation was observed was recorded.

(3) UV absorption peak

The absorbance of each UV wavelength band of the silsesquioxane resin prepared in Preparation Example was measured using a UV-Vis spectrometer (Shimadzu).

(4) yellowing Whether the phenomenon occurs

Samples prepared in Examples and Comparative Examples were sampled in a size of 10 mm * 10 mm and left for 1,000 hours in a high-temperature, high-humidity chamber at 85 ° C. and 90% relative humidity. was measured using

division pencil hardness Flexibility (mm) Chromaticity b value change rate (%) R ₁ R ₂ Example 1 9H 8 20 2.0 Example 2 9H 7 15 1.7 Example 3 9H 12 22 2.5 Example 4 9H 13 35 2.4 Example 5 8H 14 26 2.5 Example 6 9H 14 25 2.2 Example 7 9H 10 25 4.9 Example 8 9H 8 18 1.9 Example 9 8H 18 36 2.3 Example 10 9H 10 30 4.3 Example 11 9H 15 26 4.6 Example 12 9H 4 15 4.8 Example 13 7H 5 25 6.4 Example 14 7H 7 16 10.5 Comparative Example 1 5H 10 25 2.6 Comparative Example 2 5H 9 21 1.9 Comparative Example 3 4H 15 32 2.5 Comparative Example 4 4H 20 38 3.4 Comparative Example 5 4H 18 36 3.6 Comparative Example 6 5H 8 45 4.2

Referring to Table 3, the hard coating film having a hard coating layer prepared from the composition of Examples exhibited excellent hardness and flexibility. In addition, it was confirmed that the yellowing phenomenon was minimized because the change rate of the chromaticity b value was small even after heat-and-moisture treatment.

However, the hard coating film having a hard coating layer prepared from the composition of Comparative Example was significantly inferior in hardness or flexibility.

100: hard coating film 110: substrate
120: hard coating layer

Claims (12)

an epoxy siloxane resin having a weight average molecular weight of 500 to 30,000 and a polydispersity index (PDI) of 2.0 to 4.0; photoinitiators; And a composition for forming a hard coating layer comprising an acid anhydride-based thermosetting agent,
The thermosetting agent is included in an amount of 5 to 30 parts by weight based on 100 parts by weight of the siloxane resin,
After curing the composition for forming the hard coat layer, the hardness is 7H or more, the composition for forming a hard coat layer.
The composition of claim 1, wherein the siloxane resin has a weight average molecular weight of 1,000 to 20,000.
The composition of claim 1, wherein the siloxane resin has a weight average molecular weight of 5,000 to 15,000.
The composition of claim 1, wherein the siloxane resin has an epoxy group equivalent of 3.0 to 6.3 mmol/g.
The composition for forming a hard coat layer according to claim 1, wherein the siloxane resin is polymerized by including a monomer having an aryl group in an amount of 10% by weight or less based on the total weight of the monomer.
The composition for forming a hard coating layer according to claim 1, wherein the siloxane resin has a UV absorption spectrum peak having a maximum absorbance at a wavelength of 200 to 250 nm.
The composition for forming a hard coating layer according to claim 1, wherein the thermosetting agent is at least one acid anhydride-based thermosetting agent selected from the group consisting of the following formulas (1) to (15).

(Wherein, n is an integer of 0 to 5, X is an oxygen atom or a methylene group, Ra, Rb, Rc and Rd are each independently a hydrogen atom or an alkyl group having 1 to 10 carbon atoms, and Rs is a carbon number 1 to 20 of an alkylene group, an alkenylene group having 2 to 20 carbon atoms, or an arylene group having 6 to 18 carbon atoms).
The composition of claim 1, wherein the thermosetting agent is methyl-5-norbornene-2,3-dicarboxylic anhydride.
delete A hard coating film comprising a substrate having a hard coating layer formed of the composition for forming a hard coating layer of any one of claims 1 to 8 on at least one surface.
The method according to claim 10, wherein the hard coating layer is 85 ℃, 90% relative humidity conditions, the change rate of the chromaticity b value before and after 1,000 hours of standing within 5%, the hard coating film.
An image display device having the hard coating film of claim 10 .

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