KR102063050B1 - Pressure sensitive adhesive composition - Google Patents

Abstract

The present application relates to an adhesive composition, a protective film, an optical element and a display device. The adhesive composition of this application is excellent in storage stability, shows a suitable low speed and high speed peeling force after a crosslinked structure is formed, and is excellent in the balance of both. In addition, the pressure-sensitive adhesive formed by the pressure-sensitive adhesive composition exhibits re-peelability and does not leave contaminants in the adherend after peeling. Accordingly, when the pressure-sensitive adhesive composition is applied to, for example, a protective film, it exhibits an excellent protective effect and is easily peeled off at the time of high-speed peeling, which is advantageous in terms of a high-speed process, and exhibits excellent antistatic properties in the process. Can be.

Description

Adhesive composition {PRESSURE SENSITIVE ADHESIVE COMPOSITION}

The present application relates to an adhesive composition, an optical element protective film, an optical element, and a display device.

A protective film may be used to prevent dirt, such as dust, or scratches from occurring on optical elements such as polarizing plates, other plastic products, home appliances, automobiles, and the like. Protective films require proper peel force and antistatic properties.

For example, when peeling a protective film at high speed for the use of a product or the assembly of another product, it is required that the peeling force (henceforth a "high speed peeling force") is relatively low. On the other hand, the peeling force (hereinafter referred to as "low speed peeling force") at the time of peeling at a slow speed should be relatively high to show an appropriate protective function.

In addition, foreign matters such as dust may be sucked due to static electricity mainly generated when the protective film is peeled off, or, in the case of electronic products, electrostatic destruction or malfunction of the device may be caused. In particular, in recent years, as the accessories are integrated due to the spread of computers and the multifunctionality of liquid crystal TVs and mobile telephones, the problems caused by static electricity have been highlighted.

Accordingly, efforts have been made to impart an antistatic function to the pressure-sensitive adhesive contained in the protective film.

For example, in patent document 1, there exists an attempt to mix | blend an ethylene oxide modified dioctyl plasticizer with an adhesive, and to suppress generation | occurrence | production of static electricity. In addition, in patent document 2, an organic salt is added to an adhesive, and in patent document 3, a metal salt and a chelating agent are mix | blended with an adhesive. However, according to the above methods, contamination by transfer of the pressure-sensitive adhesive component to the protected product occurs, or it is difficult to suppress static electricity generated at an early stage, and the low-speed peeling force, which is particularly important for the protective function, is too low.

Japanese Laid-Open Patent Publication 1993-140519 Korean Laid-Open Patent Publication No. 2004-0030919 Korean Laid-Open Patent Publication No. 2006-0128659

The present application provides an adhesive composition, an optical element protective film, an optical element, and a display device.

Exemplary pressure-sensitive adhesive composition may include a polymer, a compound of Formula 2 and a crosslinking agent. As a polymer, the polymer of the monomer mixture containing each monomer mentioned later can be used in order to express suitable adhesive performance, antistatic performance, peeling characteristic, etc., and to prevent contamination to a to-be-adhered body especially after peeling of an adhesive. As used herein, the term monomer refers to all kinds of compounds capable of forming a polymer through a polymerization reaction. In addition, the polymer may be a polymer of a monomer mixture including a certain monomer, which may mean that the polymer contained in the monomer mixture is included as a polymer unit in the polymer. In addition, the inclusion in the polymerization unit in the above may mean a state in which the monomer is polymerized and included in the skeleton such as the side chain or the main chain of the polymer.

The polymer of the present application may be a polymer of a monomer mixture comprising an alkyl (meth) acrylate and the first and second monomers described later.

As the alkyl (meth) acrylate in the above, in consideration of the cohesive force, glass transition temperature or adhesion of the pressure-sensitive adhesive, alkyl having an alkyl group having 1 to 14 carbon atoms, 1 to 12 carbon atoms, 4 to 12 carbon atoms or 6 to 12 carbon atoms (Meth) acrylate can be used. The alkyl (meth) acrylate may be included as a main component in the monomer mixture. As included as the main component in the above it may mean that the alkyl (meth) acrylate is contained in the monomer mixture by 55% or more or 60% or more by weight. The weight ratio in the monomer mixture of the alkyl (meth) acrylate may be 100% or less, 90% or less, or 80% or less. As said monomer, methyl (meth) acrylate, ethyl (meth) acrylate, n-propyl (meth) acrylate, isopropyl (meth) acrylate, n-butyl (meth) acrylate, t-butyl (meth) Acrylate, sec-butyl (meth) acrylate, pentyl (meth) acrylate, 2-ethylhexyl (meth) acrylate, 2-ethylbutyl (meth) acrylate, n-octyl (meth) acrylate, isooctyl (Meth) acrylate, isononyl (meth) acrylate, lauryl (meth) acrylate, tetradecyl (meth) acrylate, and the like can be exemplified, and one or two or more of the above can be included in the monomer mixture. have.

The monomer mixture may further include a hydroxy group-containing monomer. The monomer may provide a hydroxyl group to the polymer.

As a hydroxyl group containing monomer, the monomer represented by following formula (1) can be illustrated, for example.

[Formula 1]

In Formula 1, Q is hydrogen or an alkyl group, for example, an alkyl or methyl group having 1 to 4 carbon atoms, A and B are each independently an alkylene group, n is any number, for example, a number of 0 to 10 to be.

As used herein, unless otherwise specified, the term alkylene group or alkylidene group may be an alkylene group or an alkylidene group having 1 to 20 carbon atoms, 1 to 16 carbon atoms, 1 to 12 carbon atoms, 1 to 8 carbon atoms, or 1 to 4 carbon atoms. have. The alkylene group or alkylidene group may be linear, branched or cyclic. The alkylene group or alkylidene group may be substituted by one or more substituents if necessary.

When two or more [—O—B—] units are present in Formula 1, the carbon number of B in the unit may be the same or different.

In Formula 1, A and B may be each independently a linear alkylene group.

As a compound of Formula 1, 2-hydroxyethyl (meth) acrylate, 2-hydroxypropyl (meth) acrylate, 4-hydroxybutyl (meth) acrylate, 6-hydroxyhexyl (meth) acrylate , 8-hydroxyoctyl (meth) acrylate, 2-hydroxyethylene glycol (meth) acrylate or 2-hydroxypropylene glycol (meth) acrylate and the like can be exemplified, but is not limited thereto.

In one example, as the hydroxyl group-containing monomer, two kinds of monomers having different carbon numbers present in the side chain may be used.

For example, the monomer mixture is represented by Formula 1 and is present in A and B of Formula 1 while being represented by Formula 1 and the first monomer having the number of carbons of alkylene groups present in Formulas A and B in the range of 1 to 3. It may include a second monomer having 4 to 20, 4 to 16, 4 to 12, 4 to 8 or 4 to 6 carbon atoms of the alkylene group.

When calculating the number of carbons to distinguish the first and second monomers in the above, only the number of carbons of the alkylene group formed in the straight chain form is considered. That is, in the case of A of Formula 1, when the oxygen atom in the parenthesis is connected to the oxygen atom on the left side of A, or when n is 0, the carbon of the linear alkylene group connecting the oxygen atom on the left side of the A The number is considered, and in the case of B, the number of carbons in the linear alkylene group connecting the oxygen atom on the left side of B and the hydroxy group on the right side is considered. Therefore, for example, when the substituent containing carbon is substituted for A and B, carbon number of the substituent is not considered. Thus, through the polymerization unit of the two kinds of hydroxy monomers can be provided a pressure-sensitive adhesive excellent in particularly excellent peel force characteristics, that is, the balance of high-speed and low-speed peel force.

The ratio of the weights of the first and second monomers in the monomer mixture may be adjusted in order to ensure peeling properties, that is, excellent balance of low speed and high speed peeling force, while ensuring various physical properties such as adhesive performance.

In the monomer mixture, the first monomer may be included in a ratio of about 0.1 to 20 parts by weight or about 0.5 to 20 parts by weight with respect to 100 parts by weight of the alkyl (meth) acrylate. In addition, the second monomer in the monomer mixture is about 0.1 to 5 parts by weight, about 1 to 5 parts by weight, about 1.5 to 5 parts by weight or about 1.5 to 4 parts by weight based on 100 parts by weight of the alkyl (meth) acrylate. May be included as a percentage of wealth. In the present specification, the unit weight part may mean a ratio of weights between components, unless otherwise specified.

Meanwhile, the ratio (A / B) of the weight (A) of the first monomer and the weight (B) of the second monomer in the monomer mixture may be 0.1 or more. In another example, the ratio may be about 0.1-20, about 0.1-15 or about 0.1-10.

It is possible to provide a pressure-sensitive adhesive which exhibits an appropriate antistatic performance within the above ranges and exhibits an appropriate balance of high speed and low speed peeling force without leaving contaminants during peeling.

The monomer mixture is, for example, a known monomer used in the preparation of the polymer of the pressure-sensitive adhesive, for example, (meth) acrylic acid, 2- (meth) acryloyloxy, if necessary for controlling the glass transition temperature. Carboxyl group-containing monomers such as acetic acid, 3- (meth) acryloyloxy propyl acid, 4- (meth) acryloyloxy butyl acid, acrylic acid duplex, itaconic acid, maleic acid and maleic anhydride; A monomer having an isocyanate group, a monomer having a glycidyl group such as glycidyl (meth) acrylate or the like, or a radical polymerizable monomer such as styrene may be further included.

The polymer is prepared by applying the above-described monomer mixture to a polymerization mode such as solution polymerization, photo polymerization, bulk polymerization, suspension polymerization or emulsion polymerization. can do. After the polymerization, the monomers included in the monomer mixture may be polymerized to form the polymerized unit.

The pressure-sensitive adhesive composition may include the polymer described above as a main component. That is, the pressure-sensitive adhesive composition, based on the weight of the solid content of the polymer at least about 55%, at least about 60%, at least about 65%, at least about 70%, at least about 75%, at least about 80%, at least about 85%, At least about 90% or at least about 95%. The weight ratio (based on solids) of the polymer in the pressure-sensitive adhesive composition may be about 100% or less, about 100% or less, or about 99% or less.

The pressure-sensitive adhesive composition may further include a compound of Formula 2 in addition to the polymer. Since such a compound has a hydroxyl group at the terminal, it may be combined with a polymer during the crosslinking reaction of the pressure-sensitive adhesive composition. Therefore, the following compound can be made to prevent the contamination to a to-be-adhered body, while showing an excellent antistatic performance with an adhesive.

[Formula 2]

In formula (2), R is a hydrogen atom or an alkyl group having 1 to 4 carbon atoms, for example, a methyl group, n is a number in the range of 0 to 32, and m is a number in the range of 5 to 50.

In Chemical Formula 2, n may be about 5 to 30 in another example, and m may be about 10 to 40 in another example.

The compound of Formula 2 may be included in a ratio of 0.1 to 5 parts by weight or 0.3 to 5 parts by weight with respect to 100 parts by weight of the polymer. In this range, the pressure-sensitive adhesive exhibits a balance of excellent antistatic property and low speed and high speed peeling force, and contamination to the adherend during peeling can be prevented.

The pressure-sensitive adhesive composition may further include an isocyanate crosslinking agent as a crosslinking agent, which may react with the crosslinking point of the polymer to implement a crosslinking structure and at the same time induce bonding between the compound of Formula 2 and the polymer.

As a crosslinking agent, an aliphatic isocyanate crosslinking agent can be used, for example. When such a crosslinking agent implements a crosslinked structure with the polymer, ie, a polymer including two or more hydroxy group-containing monomers, an adhesive having a necessary antistatic property with suitable low speed and high speed peeling force may be realized. For example, as a crosslinking agent, the crosslinking agent containing an aliphatic cyclic isocyanate compound and / or an aliphatic acyclic isocyanate compound can be used. As used herein, the term aliphatic cyclic isocyanate compound means an isocyanate compound that includes a ring structure, but the structure does not correspond to an aromatic ring, and the aliphatic acyclic isocyanate compound is, for example, an aliphatic linear or It may mean a branched isocyanate compound. As the aliphatic cyclic isocyanate compound, for example, isocyanate compounds such as isophorone diisocyanate or methylene dicyclohexyl diisocyanate or cyclohexane diisocyanate, and the like Derivatives such as dimers or trimers, or reactants of any of the above with polyols (ex. Trimethylolpropane) may be exemplified. Examples of the aliphatic acyclic isocyanate compounds include carbon atoms such as hexamethylene diisocyanate and the like. Alkylene diisocyanate compounds having from 20 to 20, 1 to 16 carbon atoms, 1 to 12 carbon atoms, or 1 to 8 carbon atoms, derivatives thereof such as dimers or trimers, or any of the above and polyols (ex. Reactant with propane) Etc. may be exemplified, but is not limited thereto.

In the case where the aliphatic cyclic isocyanate compound and the aliphatic acyclic isocyanate compound are used together, the ratio is not particularly limited and may be appropriately selected as necessary. Typically, about 1 part by weight to about 500 parts by weight or about 20 parts by weight to about 300 parts by weight of the aliphatic acyclic isocyanate compound may be included in the crosslinking agent relative to 100 parts by weight of the aliphatic cyclic isocyanate compound. As such a crosslinking agent, that is, a crosslinking agent containing an aliphatic cyclic isocyanate compound and an aliphatic acyclic isocyanate compound may be used. Examples thereof include MHG-80B manufactured by Asahi and NZ-1 manufactured by Duranate P or BAYER. There is this.

As a crosslinking agent, if necessary further above, ethylene glycol diglycidyl ether, triglycidyl ether, trimethylolpropane triglycidyl ether, N, N, N ', N'- tetraglycidyl ethylenediamine or glycerin Epoxy crosslinking agents such as diglycidyl ether and the like; N, N'-toluene-2,4-bis (1-aziridinecarboxamide), N, N'-diphenylmethane-4,4'-bis (1-aziridinecarboxamide), triethylene melamine Aziridine crosslinkers such as bisisoprotaloyl-1- (2-methylaziridine) or tri-1-aziridinylphosphineoxide, or aluminum, iron, zinc, tin, titanium, antimony, magnesium and / or vanadium A well-known crosslinking agent, such as a metal chelate crosslinking agent which is a compound in which a polyvalent metal like this is coordinated with acetyl acetone, ethyl acetoacetate, etc., can be used together.

The pressure-sensitive adhesive composition may include 1 part by weight to 15 parts by weight, about 2 to 15 parts by weight, about 3 to 15 parts by weight, about 4 to 15 parts by weight, about 4 to 13 parts by weight, or about 4 to 12 parts by weight, based on 100 parts by weight of the polymer. A negative crosslinking agent may be included. An appropriate crosslinking structure can be realized in this range, and the low speed and high speed peeling force of the pressure-sensitive adhesive can be adjusted to a desired range, and contamination of the adherend after peeling off of the pressure-sensitive adhesive can also be prevented.

In particular, the crosslinking agent may be controlled in consideration of the implementation of the crosslinking structure suitable for the use of the pressure-sensitive adhesive composition of the above-described polymer and the introduction efficiency of the compound of Formula 2.

For example, the isocyanate crosslinking agent may be included such that the equivalent amount of isocyanate group included in the crosslinking agent is in the range of 1.0 to 2.2 or 1.0 to 2.0 per equivalent of hydroxy group included in the polymer. In addition, the equivalent of the isocyanate group included in the crosslinking agent of the isocyanate crosslinking agent may be included so as to fall within the range of 1 to 2 or 1.1 to 1.8 per 1 equivalent of the hydroxy group included in the polymer and the hydroxy group of the compound of Formula 2. Within this range, a crosslinked structure suitable for use may be realized and at the same time, the introduction of the compound of Formula 2 may be effectively performed to form an adhesive having a desired physical property.

The equivalent weight of the hydroxy group contained in the polymer is determined by multiplying the number of moles of the hydroxy group-containing monomer by calculating the number of moles of the hydroxy group-containing monomer from the weight (unit: g) of the hydroxy group-containing monomer present in the polymer. It is a shame. For example, when 99 g of butyl acrylate (BA) and 1 g of 4-hydroxybutyl acrylate (4-HBA) are polymerized to prepare a polymer, the molar mass of the monomer (4-HBA) is about 144. g / mol, the mole number of the monomer (4-HBA) (1/144) is about 0.00694 mole, and the mole number of the crosslinkable functional group (hydroxy group) included in the monomer (4-HBA) is 1, The equivalent (= 0.00694 × 1) of the hydroxyl groups of the polymer is about 0.00694. In addition, the equivalent of a hydroxyl group can also be calculated | required by measuring the hydroxyl value (OH value) of a polymer, and converting the content of the hydroxyl group in molar number.

In addition, the equivalent of the hydroxyl group of the compound of Formula 2 is the same as the number of moles of the compound, since the compound of Formula 2 includes one hydroxyl group.

In addition, the equivalent of the isocyanate group of a crosslinking agent is a numerical value calculated | required by multiplying the number of moles of the crosslinking functional group which this crosslinking agent contains after obtaining the number-of-moles of the said crosslinking agent from the weight (unit: g) of the crosslinking agent used. For example, when the crosslinking agent is trifunctional having three crosslinkable functional groups (isocyanate groups) and 0.4 g of a crosslinking agent having a molar mass of about 308 g / mol, the number of moles of the crosslinking agent per 100 g of the solid content (0.4 / 308 ) Is about 0.0012987 mol, and the number of moles of the crosslinkable functional group (isocyanate group) included in the crosslinking agent is 3, so that the equivalent (= 0.0012987 x 3) of the crosslinking agent is about 0.00390.

The pressure-sensitive adhesive composition may further include an antistatic agent. As the antistatic agent, for example, an ionic compound can be used. As an ionic compound, a metal salt or an organic salt can be used, for example.

Metal salts may include, for example, alkali metal cations or alkaline earth metal cations. As the cation, lithium ion (Li ⁺ ), sodium ion (Na ⁺ ), potassium ion (K ⁺ ), rubidium ion (Rb ⁺ ), cesium ion (Cs ⁺ ), beryllium ion (Be ²⁺ ), magnesium ion ( Mg ²⁺ ), calcium ions (Ca ²⁺ ), strontium ions (Sr ²⁺ ), and barium ions (Ba ²⁺ ) may be exemplified by one kind or two or more kinds thereof. For example, lithium ions, sodium ions, Lithium ions may be used in consideration of one or more kinds of potassium ions, magnesium ions, calcium ions and barium ions, or ionic stability and mobility.

As the anion contained in the ionic compound is _{^{PF 6 -, AsF -, NO}} 2 -, fluoride (F ^-), chloride (Cl ^-), bromide (Br ^-), iodide (I ^-), perchlorate (ClO ₄ ^-), hydroxide (OH ^-), carbonate (CO ₃ ^2-), nitrate (NO ₃ ^-), trifluoromethane sulfonate (CF ₃ SO ₃ ^-), sulfonate (SO ₄ ^-), hexafluorophosphate (PF ₆ ^-), methyl benzene sulfonate _{(CH 3 (C 6 H 4} ) SO 3 -), p- toluenesulfonate _{(CH 3 C 6 H 4 SO} 3 -), tetraborate (B ₄ O ₇ ^2- ), carboxybenzenesulfonate (COOH (C ₆ H ₄ ) SO ₃ ⁻ ), trichloromethanesulfonate (CF ₃ SO ₂ ⁻ ), benzoate (C ₆ H ₅ COO ⁻ ), acetate ( a), a triple acetate _{^{- CH 3 COO (CF 3 COO}} -), tetrafluoroborate (BF ₄ ^-), tetra-benzyl borate _{(B (C 6 H 5)} 4 -) or tris pentafluoroethyl trifluoromethyl phosphate _{(P (C 2 F 5)} 3 F 3 -) or the like can be illustrated.

In another example, an anion or bisfluorosulfonylimide represented by the following Chemical Formula 5 may be used as the anion.

[Formula 5]

[X (YO _m R _f ) _n ] ^-

In formula (5), X is a nitrogen atom or a carbon atom, Y is a carbon atom or a sulfur atom, R _f is a perfluoroalkyl group, m is 1 or 2, and n is 2 or 3.

In Formula 5, when Y is carbon, m is 1, when Y is sulfur, m is 2, n is 2 when X is nitrogen, and n may be 3 when X is carbon.

Anions or bis (fluorosulfonyl) imides of formula (5) exhibit high electronegativity due to perfluoroalkyl groups (R _f ) or fluorine groups, and also include unique resonance structures, forming weak bonds with cations At the same time, it has hydrophobicity. Therefore, while an ionic compound shows the outstanding compatibility with other components of compositions, such as a polymer, it can provide high antistatic property even with a small amount.

R _f of Formula 5 may be a perfluoroalkyl group having 1 to 20 carbon atoms, 1 to 12 carbon atoms, 1 to 8 carbon atoms or 1 to 4 carbon atoms, in which case the perfluoroalkyl group is linear, branched or It may have a cyclic structure. The anion of Formula 5 may be a sulfonyl metide, sulfonylimide, carbonyl metide, or carbonyl imide anion, and specifically, tristrifluoromethanesulfonylmethide and bistrifluoromethanesulfide Ponylimide, bisperfluorobutanesulfonylimide, bispentafluoroethanesulfonylimide, tristrifluoromethanecarbonylmide, bisperfluorobutanecarbonylimide or bispentafluoroethanecarbonyl It may be a kind of imide or the like or a mixture of two or more thereof.

As the ionic compound, for example, as a cation, N-ethyl-N, N-dimethyl-N-propylammonium, N, N, N-trimethyl-N-propylammonium, N-methyl-N, N, N -Tributylammonium, N-ethyl-N, N, N-tributylammonium, N-methyl-N, N, N-trihexylammonium, N-ethyl-N, N, N-trihexylammonium, N-methyl Quaternary ammonium such as -N, N, N-trioctylammonium or N-ethyl-N, N, N-trioctylammonium, phosphonium, pyridinium, imidazolium, blood An organic salt containing pyrolidinium, piperidinium, or the like together with the anion component may be used, or the metal salt and the organic salt may be used in combination if necessary.

The content of the ionic compound in the pressure-sensitive adhesive composition is not particularly limited, for example, may be present in a ratio of 0.1 parts by weight to 5 parts by weight with respect to 100 parts by weight of the polymer. The ratio of the ionic compound can be changed in consideration of the desired antistatic property or compatibility between the components.

The pressure-sensitive adhesive composition may include a light stabilizer, for example, a light stabilizer such as a hindered amine compound. Such light stabilizers do not aggregate even when the pressure-sensitive adhesive is left at high temperature, for example, so that the concentration of the antistatic agent described later in the aggregated cluster does not increase, and the compound of Formula 2 included in the polymer is included. It is possible to prevent the problem that the ether-bonding site of is decomposed by heat to generate radicals or the hydroxy group-containing monomer causes a condensation reaction, thereby greatly improving the storage stability of the pressure-sensitive adhesive composition.

As an optical stabilizer, the compound represented by following formula (3) can be illustrated, for example.

[Formula 3]

In Formula 3, M ₁ to M ₅ are each independently R ₁ -N, (R ₂ ) (R ₃ ) -C or (R ₄ ) (R ₅ ) -C, wherein R ₁ is a hydrogen atom, an alkyl group or An alkoxy group, R ₂ and R ₃ are each independently an alkyl group, R ₄ and R ₅ are each independently a hydrogen atom or an alkyl group, L is an alkylene group or an alkylidene group, P is an alkyl group or a substituent of the formula to be. In the above formula (3) at least one of M ₂ to M ₄ is wherein R ₁ -N, R ₁ -N of M _2, M ₃ or M _1, present immediately adjacent to M ₄ M _2, M _3, M ₄ Or M ₅ may be (R ₂ ) (R ₃ ) -C.

[Formula 4]

In Formula 4, M ₆ to M ₁₀ are each independently R ₁ -N, (R ₂ ) (R ₃ ) -C or (R ₄ ) (R ₅ ) -C, wherein R ₁ is a hydrogen atom, an alkyl group or An alkoxy group, R ₂ and R ₃ are each independently an alkyl group, and R ₄ and R ₅ are each independently a hydrogen atom or an alkyl group. In the above formula (4) at least one of M ₇ to M ₉ is the _{R 1 -N, M 7, M} 8 or _{M M 6, M 7, M} 8, M 9 or M ₁₀ immediately adjacent to the existing ₉ is the (R ₂ ) (R ₃ ) -C.

In Formulas 3 and 4, M ₁ to M ₁₀ are R ₁ -N, (R ₂ ) (R ₃ ) -C or (R ₄ ) (R ₅ ) -C, which is nitrogen at the position of M ₁ to M ₁₀ . An atom (N) or a carbon atom (C) is present, and may refer to a form in which a substituent such as R ₁ to R ₅ is bonded to the nitrogen atom or carbon atom.

는 상기 부호와 연결되어 있는 화학식 4의 탄소 원자가 화학식 3의 산소 원자에 결합되어 있는 것을 의미한다.In addition, in the formula (4)

Means that the carbon atom of formula (4) linked with the above sign is bonded to the oxygen atom of formula (3).

In Formula 3, L, which is an alkylene group or an alkylidene group, may be substituted or unsubstituted if necessary. For example, L may be substituted with an aryl group, and the aryl group may be exemplified by 3,5-bis (1,1-dimethylethyl) -4-hydroxyphenyl group, but is not limited thereto. It is not.

R ₁ in Formula 3 may be, for example, a hydrogen atom, an alkyl group having 1 to 8 carbon atoms or an alkyl group having 1 to 4 carbon atoms, an alkoxy group having 4 to 16 carbon atoms or 4 to 12 carbon atoms. The alkyl group or alkoxy group may be linear or branched, and may be substituted by one or more substituents.

In Formula 3, R ₂ , R ₃ and P may each independently be an alkyl group having 1 to 12 carbon atoms, 1 to 8 carbon atoms, or 1 to 4 carbon atoms. The alkyl group may be linear or branched, and may be substituted by one or more substituents.

In addition, in Formula 3, R ₄ and R ₅ may be a hydrogen atom.

In Formula 3, L may be, for example, an alkylene group having 4 to 12 carbon atoms or 6 to 10 carbon atoms, or an alkylidene group having 2 to 10 carbon atoms or 4 to 8 carbon atoms. The alkylene group or alkylidene group may be linear or branched, and may be substituted by one or more substituents.

As the compound of the formula (3), for example, bis (1,2,2,6,6-pentamethyl-4-piperidyl) sebacate (bis (1,2,2,6,6-pentamethyl-4) -piperidyl) sebacate), methyl 1,2,2,6,6-pentamethyl-4-piperidyl sebacate, propanedioic acid 2-[[3,5-bis (1,1-dimethylethyl) -4-hydroxyphenyl] methyl] -2-butyl-1,3-bis (1,2,2,6,6-pentamethyl- 4-piperidinyl) ester (propanedioic acid, 2-[[3,5-bis (1,1-dimethylethyl) -4-hydroxyphenyl] methyl] -2-butyl-1,3-bis (1,2,2 (6,6-pentamethyl-4-piperidinyl) ester), bis (2,2,6,6-tetramethyl-4-piperidyl) sebacate (bis (2,2,6,6-tetramethyl-4- piperidyl) sebacate) or bis (1-octyloxy-2,2,6,6-tetramethyl-4-piperidinyl) sebacate (bis- (1-octyloxy-2,2,6,6-tetramethyl-4 -piperidinyl) sebacate) and the like can be exemplified, but is not limited thereto.

The compound of Formula 3 may be included in the pressure-sensitive adhesive composition, for example, about 0.05 parts by weight to 5 parts by weight based on 100 parts by weight of the polymer. Under such a ratio, it is possible to effectively prevent generation of the radicals, condensation of hydroxy group-containing monomers, and the like, and to provide an adhesive composition having excellent storage stability.

The pressure-sensitive adhesive composition also includes a coordination compound, a photoinitiator, a polyfunctional acrylate, an epoxy resin, which can form a coordination bond with a silane coupling agent, a tackifier, the antistatic agent, and so on, without affecting the effect of the application. It may further comprise one or more additives selected from the group consisting of crosslinkers, ultraviolet stabilizers, antioxidants, colorants, reinforcing agents, fillers, defoamers, surfactants and plasticizers.

The pressure-sensitive adhesive composition has a low-speed peeling force of about 1 gf / 25 mm to 40 gf / 25mm, 1 gf / 25mm to 30 gf / 25mm, 1 for an adherend having a surface energy of 30 mN / m or less in a crosslinked structure. gf / 25mm to 20 gf / 25mm or 1 gf / 25mm to 10 gf / 25mm and have high speed peeling force of 10 gf / 25mm to 300 gf / 25mm, 10 gf / 25mm to 250 gf / 25mm, 10 gf / 25mm to 200 gf / 25mm, 10 gf / 25mm to 150 gf / 25mm, 10 gf / 25mm to 100 gf / 25mm, about 20 gf / 25mm to 100 gf / 25mm, about 30 gf / 25mm to 100 gf / 25mm, about 40 gf / 25mm to 100 gf / 25mm or about 50 gf / 25mm to 100 gf / 25mm.

As used herein, the term low speed peel force is a peel force measured at a peel angle of 180 degrees and a peel rate of 0.3 m / min, and a high speed peel force is measured at a peel angle of 180 degrees and a peel rate of 30 m / min. May be a peel force.

Specifically, each of the peeling force, the pressure-sensitive adhesive composition having a crosslinked structure is attached to the adherend having a surface energy of 30 mN / m or less, and maintained for 24 hours at a temperature of 23 ℃ and 65% relative humidity It may be measured at each peeling angle and peeling rate. The specific way of measuring each peel force is described in the following Examples.

The method of measuring the surface energy of the adherend is not particularly limited, and a known method of measuring the surface energy may be applied. For example, the contact angle of an adherend can be measured and surface energy can be calculated | required from this, or it can measure using a well-known surface energy measuring equipment. The surface energy of the adherend may be, for example, about 10 m / N / m to about 30 mN / m.

The pressure-sensitive adhesive composition also has a ratio (H / L) of the high speed peeling force (H) to the low speed peeling force (L) of 1 to 30, 1 to 25, 1 to 20, 5 to 20, about 10 to 20, About 13 to 17 degrees.

When the low-speed peeling force, high-speed peeling force and / or peeling voltage is secured as described above, it can be easily peeled off at high speed while minimizing the occurrence of static electricity and the like while exhibiting an appropriate protection function for the adherend.

The present application also relates to an adhesive sheet. The said adhesive sheet can be a protective film, specifically, the protective film for optical elements.

For example, the adhesive sheet can be used as a protective film for optical elements, such as a polarizing plate, a polarizer, a polarizer protective film, retardation film, a viewing angle compensation film, and a brightness enhancement film. As used herein, the terms polarizer and polarizer refer to objects that are distinguished from each other. That is, the polarizer refers to the film, sheet or device itself exhibiting a polarizing function, and the polarizing plate means an optical element including other elements together with the polarizer. As other elements that may be included in the optical device together with the polarizer, a polarizer protective film or a retardation layer may be exemplified, but is not limited thereto.

The pressure-sensitive adhesive sheet may include, for example, a base film for surface protection and an adhesive layer present on one side of the base film. The pressure-sensitive adhesive layer may include, for example, a crosslinked pressure-sensitive adhesive composition, that is, a pressure-sensitive adhesive composition having a crosslinked structure as the pressure-sensitive adhesive composition.

The pressure-sensitive adhesive composition exhibits a relatively high low-speed peeling force and a relatively low high-speed peeling force after the crosslinking structure is implemented, and is excellent in balance of both peeling forces, and has excellent durability, workability, transparency, and antistatic property. Accordingly, the protective film protects the surface of optical elements such as polarizing plates, retardation plates, optical compensation films, reflective sheets, and luminance enhancing films used in various optical devices or components or display devices or components, for example, LCDs. It can be effectively used as a surface protective film for, but the above use is not limited to the protective film.

As the surface protective base film, a general film or sheet known in the art may be used. For example, polyester films such as polyethylene terephthalate or polybutylene terephthalate, polytetrafluoroethylene film, polyethylene film, polypropylene film, polybutene film, polybutadiene film, poly (vinyl chloride) film or polyimide film Plastic films such as Such a film may consist of a single layer, or two or more layers may be laminated, and in some cases, may further include a functional layer such as an antifouling layer or an antistatic layer. In addition, from the viewpoint of improving the substrate adhesion, one or both surfaces of the substrate may be subjected to surface treatment such as primer treatment.

The thickness of the base film is not particularly limited to be appropriately selected depending on the use, and can be generally formed in a thickness of 5 μm to 500 μm or 10 μm to 100 μm.

The thickness of the pressure-sensitive adhesive layer included in the pressure-sensitive adhesive sheet is not particularly limited, and may be, for example, 2 μm to 100 μm or 5 μm to 50 μm.

The method for forming the pressure-sensitive adhesive layer is not particularly limited, and for example, the pressure-sensitive adhesive composition or a coating liquid prepared therefrom is applied to a base film or the like by a conventional means such as a bar coater, and cured, or the pressure-sensitive adhesive composition or coating liquid is once peelable. The method etc. which apply | coat to the surface of a base material, harden | cure, and transfer again to a base film can be used.

The formation process of the pressure-sensitive adhesive layer is preferably performed after sufficiently removing the bubble-inducing component such as volatile components or reaction residues in the pressure-sensitive adhesive composition or coating liquid. Accordingly, the crosslinking density or molecular weight of the pressure-sensitive adhesive is too low, the elastic modulus is lowered, the bubbles existing between the glass plate and the pressure-sensitive adhesive layer in the high temperature state is increased, it is possible to prevent the problem of forming a scattering body therein.

In addition, the method of curing the pressure-sensitive adhesive composition in the above process is not particularly limited, for example, the polymer and the cross-linking agent included in the composition may be subjected to an appropriate aging process, or to induce the activation of a photoinitiator therein. Light irradiation, for example, ultraviolet light irradiation can be carried out.

For example, the pressure-sensitive adhesive layer may have a gel content of about 80% to about 99%. The gel content can be calculated, for example, by the following formula (1).

[Equation 1]

Gel content = B / A × 100

In Equation 1, A represents the mass of the pressure-sensitive adhesive, B represents the dry mass of the insoluble fraction recovered after immersing the pressure-sensitive adhesive in ethyl acetate for 48 hours at room temperature.

The present application also relates to an optical device. An exemplary optical element may include an optical element and the adhesive sheet attached to a surface of the optical element. For example, the pressure-sensitive adhesive layer of the pressure-sensitive adhesive sheet is attached to the surface of the optical element, thereby the optical element can be protected by the surface protection base film.

As an optical element contained in an optical element, a polarizer, a polarizing plate, a polarizer protective film, a retardation layer, a viewing angle compensation layer, etc. can be illustrated, for example.

As the polarizer as described above, for example, a general kind known in the art, such as a polyvinyl alcohol polarizer, may be employed without limitation.

The polarizer is a functional film or sheet capable of extracting only light vibrating in one direction from incident light while vibrating in various directions. Such a polarizer may be, for example, a form in which a dichroic dye is adsorbed in a polyvinyl alcohol-based resin film. Polyvinyl alcohol-type resin which comprises a polarizer can be obtained by gelatinizing polyvinylacetate-type resin, for example. In this case, the polyvinylacetate resin which can be used may include not only a homopolymer of vinyl acetate but also a copolymer of vinyl acetate and other monomers copolymerizable with the above. Examples of the monomer copolymerizable with vinyl acetate include unsaturated carboxylic acids, olefins, vinyl ethers, unsaturated sulfonic acids, and a mixture of one or two or more kinds of acrylamides having an ammonium group, but are not limited thereto. no. The degree of gelation of the polyvinyl alcohol-based resin is usually 85 mol% to 100 mol%, preferably 98 mol% or more. The polyvinyl alcohol-based resin may be further modified, for example, polyvinyl formal or polyvinyl acetal modified with aldehydes may be used. In addition, the degree of polymerization of the polyvinyl alcohol-based resin may be about 1,000 to 10,000, preferably about 1,500 to 5,000.

Polyvinyl alcohol-type resin is formed into a film, and can be used as a raw film of a polarizer. The method of forming a polyvinyl alcohol-type resin into a film is not specifically limited, The general method known in this field can be used. The thickness of the raw film formed into a polyvinyl alcohol-based resin is not particularly limited, and may be appropriately controlled within, for example, 1 µm to 150 µm. In consideration of ease of stretching and the like, the thickness of the master film can be controlled to 10 ㎛ or more. The polarizer is a step of stretching (ex. Uniaxial stretching) the polyvinyl alcohol resin film as described above, a step of dyeing the polyvinyl alcohol resin film with a dichroic dye, adsorbing the dichroic dye, and a dichroic dye adsorbed. The polyvinyl alcohol-based resin film can be produced through a process of treating with a boric acid aqueous solution and a process of washing with water after treating with a boric acid aqueous solution. As the dichroic dye, iodine or a dichroic organic dye may be used.

The polarizing plate may include, for example, the polarizer; And it may include another optical film attached to one side or both sides of the polarizer. As another optical film, the above-described polarizer protective film, a retardation layer, a viewing angle compensation layer, an antiglare layer, and the like can be exemplified.

A polarizer protective film is a protective film with respect to a polarizer by the concept distinguished from the protective film containing the said adhesive layer in the above. As a polarizer protective film, For example, Cellulose-type films, such as triacetyl cellulose; Acrylic film; Polyester film such as polycarbonate film or polyethylene terephthalate film; Polyether sulfone-based film; And / or a protective film composed of a polyethylene film, a polypropylene film or a polyolefin film having a cyclo or norbornene structure, or a polyolefin film such as an ethylene propylene copolymer. The thickness of the protective film is also not particularly limited, and may be formed to a conventional thickness.

In the optical device, a surface treatment layer may exist on the surface of the optical device protected by the protective film. For example, the surface treatment layer may have a surface energy of 30 mN / m or less. That is, a surface treatment layer having a surface energy of 30 mN / m or less is formed on the surface of the optical element protected by the protective film in the optical element, and the pressure-sensitive adhesive layer of the protective film is attached to the surface treatment layer. Can be.

The surface treatment layer may include a high hardness layer, an anti-glare layer such as an AG (anti-glare) layer or a semi-glare (SG) layer, or a low reflection layer such as an anti reflection (AR) layer or a low reflection (LR) layer. May be exemplified.

The high hardness layer may be a layer having a pencil hardness of at least 1H or at least 2H under a load of 500 g. Pencil hardness can be measured according to the ASTM D 3363 standard, for example using the pencil lead defined in KS G2603.

The high hardness layer may be, for example, a high hardness resin layer. The resin layer may include, for example, a room temperature curing type, a moisture curing type, a thermosetting type, or an active energy ray curable resin composition in a cured state. In one example, the resin layer may include a thermosetting or active energy ray-curable resin composition, or an active energy ray-curable resin composition in a cured state. In the description of the high hardness layer, the "cured state" may mean a case where the components contained in the respective resin compositions are converted into a hard state through a crosslinking reaction or a polymerization reaction. Further, in the above-mentioned room temperature curing type, moisture curing type, thermosetting type or active energy ray-curable resin composition, the cured state may be induced at room temperature or may be induced by application of heat or irradiation of active energy ray in the presence of appropriate moisture. By composition may be meant.

In this field, various resin compositions are known which can satisfy the pencil hardness in the above-mentioned range in a cured state, and the average technician can easily select a suitable resin composition.

In one example, the resin composition may include an acrylic compound, an epoxy compound, a urethane compound, a phenol compound, a polyester compound, or the like as a main material. In the above, the "compound" may be a monomeric, oligomeric or polymeric compound.

In one example, as the resin composition, an acrylic resin composition excellent in optical properties such as transparency and excellent in resistance to yellowing, for example, an active energy ray-curable acrylic resin composition can be used.

The active energy ray-curable acrylic composition may include, for example, an active energy ray polymerizable polymer component and a monomer for reactive dilution.

The polymer component may include a component known in the art as a so-called active energy ray polymerizable oligomer such as urethane acrylate, epoxy acrylate, ether acrylate or ester acrylate, or a monomer such as a (meth) acrylic acid ester monomer or the like. Polymerizations of the mixture can be exemplified. As the (meth) acrylic acid ester monomer, alkyl (meth) acrylate, (meth) acrylate having an aromatic group, heterocyclic (meth) acrylate or alkoxy (meth) acrylate and the like can be exemplified. Various polymer components are known in the art for preparing active energy radiation curable compositions, and such compounds may be selected as needed.

As the monomer for reactive dilution, which may be included in the active energy ray-curable acrylic composition, a monomer having one or two or more active energy ray-curable functional groups, for example, acryloyl group or methacryloyl group, may be exemplified. . As the monomer for reactive dilution, for example, the (meth) acrylic acid ester monomer or polyfunctional acrylate may be used.

The selection of the above components or the blending ratio of the selected components for producing the active energy ray-curable acrylic composition is not particularly limited and may be adjusted in consideration of the hardness and other physical properties of the desired resin layer.

As an anti-glare layer such as an AG layer or an SG layer, for example, a resin layer having a refractive index different from that of the resin layer may be used as the resin layer including the resin layer or the particles having the uneven surface formed thereon. Can be.

As said resin layer, the resin layer used for formation of the said high hardness layer can be used, for example. When forming an anti-glare layer, although it is not necessary to adjust the component of a resin composition so that a resin layer may show high hardness, you may form a resin layer so that a high hardness may be shown.

The method of forming the uneven surface on the resin layer is not particularly limited. For example, the resin composition may be cured in a state in which the coating layer of the resin composition is brought into contact with a mold having a desired uneven structure, or a particle having an appropriate particle size may be blended, coated and cured in the resin composition to realize the uneven structure. have.

The anti-glare layer can also be implemented using particles having a refractive index different from that of the resin layer.

In one example, the particles, for example, the difference in refractive index with the resin layer may be 0.03 or less or 0.02 to 0.2. If the difference in the refractive index is too small, it is difficult to cause haze, and if the difference is too large, scattering in the resin layer may occur, increasing haze, but deterioration of light transmittance or contrast characteristics may be induced. Consideration can be given to selecting appropriate particles.

The shape of the particles contained in the resin layer is not particularly limited, and may be, for example, spherical, elliptical, polyhedral, amorphous or other shapes. The particles may have an average diameter of 50 nm to 5,000 nm. In one example, the particle | grains in which the unevenness | corrugation is formed in the surface can be used as said particle | grain. Such particles have, for example, an average surface roughness (Rz) of 10 nm to 50 nm or 20 nm to 40 nm, and / or a maximum height of irregularities formed on the surface of about 100 nm to 500 nm or 200 nm to 400 nm, and the width of the unevenness may be 400 nm to 1,200 nm or 600 nm to 1,000 nm. Such particles are excellent in compatibility with the resin layer or dispersibility therein.

As the particles, various inorganic or organic particles can be exemplified. Examples of the inorganic particles include silica, amorphous titania, amorphous zirconia, indium oxide, alumina, amorphous zinc oxide, amorphous cerium oxide, barium oxide, calcium carbonate, amorphous barium titanate or barium sulfate, and the like. Examples of the organic particles may include particles including a crosslinked or uncrosslinked material of an organic material such as an acrylic resin, a styrene resin, a urethane resin, a melamine resin, a benzoguanamine resin, an epoxy resin, or a silicone resin, but are not limited thereto. It is not.

The content of the uneven structure or the particles formed in the resin layer is not particularly limited. The shape of the uneven structure or the content of the particles, for example, in the case of the AG layer, so that the haze (haze) of the resin layer is about 5% to 15%, 7% to 13% or about 10% In the case of the SG layer, the haze may be adjusted to be about 1% to 3%. The haze can be measured according to the manufacturer's manual using a hazemeter such as, for example, HR-100 or HM-150 of Sepung.

The low reflection layer, such as an AR layer or an LR layer, may be formed by coating a low refractive material. There are a variety of low refractive materials that can form a low reflection layer, all of which may be appropriately selected and used in the optical element. The low reflection layer may be formed such that the reflectance is about 1% or less through the coating of the low refractive material.

In the formation of the surface treatment layer, Korean Unexamined Patent Publication Nos. 2007-0101001, 2011-0095464, 2011-0095004, 2011-0095820, 2000-0019116, 2000-0009647, and 2000 -0018983, 2003-0068335, 2002-0066505, 2002-0008267, 2001-0111362, 2004-0083916, 2004-0085484, 2008-0005722, 2008-0063107 The materials known from Japanese Patent Application No. 2008-0101801 or 2009-0049557 may also be used.

The surface treatment layer may be formed alone or in combination of two or more thereof. As an example of the combination, the case where a high hardness layer is formed first on the surface of a base material layer and a low reflection layer is formed again on the surface can be illustrated.

The present application also relates to a display device, such as a liquid crystal display (LCD). The exemplary display device may include a liquid crystal panel, and the optical element may be attached to one side or both sides of the liquid crystal panel. The film may be attached to the liquid crystal panel using, for example, an adhesive or an adhesive. In the above, an adhesive agent or an adhesive agent is an adhesive agent or adhesive other than the adhesive agent which exists in the above-mentioned protective film.

The kind of liquid crystal panel contained in a liquid crystal display device is not specifically limited. For example, F various passive matrix systems including, but not limited to, TN (Twisted Neumatic), STN (Super Twisted Neumatic), F (ferroelectric), PD (polymer dispersed LCD), and the like; Various active matrix schemes including two terminals and three terminals; Both known liquid crystal panels, including IPS mode panels and VA mode panels, can be applied. In addition, the type of the other components included in the liquid crystal display device and the manufacturing method thereof are not particularly limited, and the general configurations in this field can be employed without limitation.

The adhesive composition of this application is excellent in storage stability, shows a suitable low speed and high speed peeling force after a crosslinked structure is formed, and is excellent in the balance of both. In addition, the pressure-sensitive adhesive formed by the pressure-sensitive adhesive composition exhibits re-peelability and does not leave contaminants in the adherend after peeling. Accordingly, when the pressure-sensitive adhesive composition is applied to, for example, a protective film, it exhibits an excellent protective effect and is easily peeled off at the time of high-speed peeling, which is advantageous in terms of a high-speed process, and exhibits excellent antistatic properties in the process. Can be.

Hereinafter, the pressure-sensitive adhesive composition will be described in more detail with reference to Examples and Comparative Examples, but the scope of the pressure-sensitive adhesive composition is not limited to the following Examples.

1. Measurement of low speed peeling force

The pressure-sensitive adhesive sheets prepared in Examples and Comparative Examples were attached to the anti-glare film (trade name: AR1, LG Chemical) with a roller of 2 Kg according to JIS Z 0237. The anti-glare film to which the adhesive sheet was attached was cut to have a length of 25 mm and a length of 100 mm, and stored for 24 hours at a temperature of 23 ° C. and a relative humidity of 65%. Then, using a tensile tester (Texture Analyzer, Stable Microsystem) at room temperature, the peeling force was measured while peeling the adhesive sheet in the longitudinal direction at a peel angle of 180 degrees and peeling rate of 0.3 m / min in the anti-glare film. Peel force was measured on two identical specimens and then the average value was employed.

2. Measurement of high speed peeling force

The pressure-sensitive adhesive sheets prepared in Examples and Comparative Examples were attached to the anti-glare film (trade name: AR1, LG Chemical) with a roller of 2 Kg according to JIS Z 0237. The anti-glare film with the adhesive sheet was cut to have a length of 25 mm and a length of 100 mm, and stored for 24 hours at a temperature of 23 ° C. and a relative humidity of 65%. Then, using a tensile tester (Texture Analyzer, Stable Microsystem) at room temperature, the peeling force was measured while peeling the adhesive sheet in the longitudinal direction at a peel angle of 180 degrees and peeling rate of 30 m / min in the anti-glare film. Peel force was measured on two identical specimens and then the average value was employed.

3. Measurement of peeling electrification voltage (ESD)

Each pressure-sensitive adhesive sheet prepared in Examples or Comparative Examples was cut to have a length of 220 mm and a length of 250 mm. The cut adhesive sheet was attached to the anti-glare film (trade name: AR1, LG Chemical) with a roller of 2 Kg according to JIS Z 0237. Thereafter, the pressure sensitive adhesive sheet was peeled off at a peel angle of 180 degrees and a peel rate of 40 m / min in an antiglare film at a temperature of 23 ° C. and a relative humidity of 65%. The peeling electrification voltage was measured using the electrostatic potential meter (KSD-200) at a distance of 40 mm from the surface of the anti-glare film immediately after the peeling.

4. Pollution Assessment

Each pressure-sensitive adhesive sheet prepared in Examples or Comparative Examples was cut to have a length of 150 mm and a length of 250 mm. The cut adhesive sheet was attached to the anti-glare film (trade name: AR1, LG Chemical) with a roller of 2 Kg according to JIS Z 0237. Thereafter, a black adhesive film was attached to the surface of the anti-glare film to which the adhesive sheet was not attached, and stored at room temperature for 24 hours. Subsequently, the pressure-sensitive adhesive sheet was peeled off, and after being left to stand at a temperature of 60 ° C. and 90% relative humidity for 1 hour, the Xenon HID lamp (Polarion) was illuminated to confirm the presence or absence of contaminants formed on the anti-glare film and evaluated according to the following criteria.

<Evaluation Criteria>

A: No pollution

B: In case of contamination

Preparation Example 1 Preparation of Acrylic Polymer (A)

2-ethylhexyl acrylate (2-EHA), 4-hydroxybutyl acrylate (4-HBA) and 2-hydroxyethyl in a 1 L reactor with nitrogen gas refluxed and a chiller installed to facilitate temperature control Acrylate (2-HEA) was added in a weight ratio of 98: 1.5: 0.5 (2-EHA: 4-HBA: 2-HEA) and 100 parts by weight of ethyl acetate was added as a solvent. Nitrogen gas was then purged for 1 hour to remove oxygen and the temperature was maintained at 60 ° C. Thereafter, a reaction initiator (AIBN: azobisisobutyronitrile) was added thereto to react for about 8 hours, and then the reaction product was diluted with ethyl acetate to prepare an acrylic polymer (A) having a solid content of about 45 wt% and a viscosity of about 2800 cP. .

Preparation Examples 2 to 7 Preparation of Acrylic Polymers (B) to (G)

An acrylic polymer was prepared in the same manner as in Preparation Example 1, except that the weight ratio of the monomer was changed as in Table 1 in the preparation of the polymer.

As a result of preparing such a polymer, the polymers of Preparation Examples 1 to 6 were observed to be transparent in appearance, but in the case of Polymer (G) of Preparation Example 7, the appearance was opaque due to phase separation, and therefore, the application of the polymer was impossible. It was confirmed that.

Production Example One 2 3 4 5 6 7 polymer A B C D E F G 2-EHA 98 94 82.5 89.5 78 83.5 91 BA 10 2-HEA 0.5 3 6 9 0.5 15 3 4-HBA 1.5 3 1.5 1.5 1.5 1.5 3 EOEOEA 20 PME 3 Solid content 45 45 45 45 45 45 45 Viscosity 2800 3100 3500 3300 2600 3900 3900 Exterior Transparency Transparency Transparency Transparency Transparency Transparency opacity Content unit: parts by weight
2-EHA: 2-ethylhexyl acrylate
BA: Butyl Acrylate
4-HBA: 4-hydroxybutyl acrylate
2-HEA: 2-hydroxyethyl acrylate
EOEOEA: ethoxyethoxyethyl acrylate
PME (Blemmer PME-2000): methoxy polyethyleneglycol monomethacrylate (ethylene oxide added mole number: 23, Japanese oil and fat company)
Solids Unit: Weight%, Viscosity Unit: cP

Example 1.

Preparation of pressure-sensitive adhesive composition

4 parts by weight of a mixture of an isoborone diisocyanate-based crosslinking agent and a hexamethylene diisocyanate-based crosslinking agent (MHG-80B manufactured by Asahi) as a crosslinking agent with respect to 100 parts by weight of the acrylic polymer (A) of Preparation Example 1, the compound of Formula 2 ( PEL-20A, in Formula 2, R is an ethyl group, m is between about 14 and 15, n is between 9 and 10, 1.0 parts by weight of Japan Carlit, LiTFSi (lithium bis (trifluoromethanesulfonyl) imide) 1 weight Part and 5 parts by weight of acetylacetone were uniformly mixed, and diluted to an appropriate concentration in consideration of coating properties to prepare an adhesive composition.

Preparation of Adhesive Sheet

The pressure-sensitive adhesive composition was coated and dried on one surface of a poly (ethylene terephthalate) PET film (thickness: 38 μm) to form a uniform coating layer having a thickness of about 20 μm. Subsequently, maintained at about 90 ℃ for about 3 minutes to induce a cross-linking reaction to the coating layer, by attaching a release PET (poly (ethylene terephthalate)) film on the coating layer to prepare an adhesive sheet.

Examples 2-5 and Comparative Examples 1-5

An adhesive composition was prepared in the same manner as in Example 1 except that the composition of the adhesive composition was changed as in Table 2 below.

Example Comparative example One 2 3 4 5 One 2 3 4 5 polymer
Kinds A A B C D A A D E F ratio 100 100 100 100 100 100 100 100 100 100 Crosslinking agent ratio 4 4.5 7 8.5 15 3.5 6 6 5 15 PEL20A ratio One 0.5 0.3 5 PEL25 ratio 3 0.5 5 PEGEH ratio One LiTFSi ratio One 2 0.2 0.2 0.5 One One 0.5 One One AA ratio 5 5 5 5 5 5 5 5 5 5 Equivalence ratio 1 2 2.3 1.2 1.1 1.4 1.8 3.0 0.6 2.5 0.9 Equivalence ratio 2 1.7 1.5 1.1 1.0 1.3 1.8 1.5 0.5 2.5 0.9 Rate unit: parts by weight
Crosslinking agent: A mixture of an isoboron diisocyanate crosslinking agent and a hexamethylene diisocyanate crosslinking agent (MHG-80B, manufactured by Ashahi)
PEL20A: In the formula (2), R is an ethyl group, m is between about 14 to 15, and n is about 9 to 10 (manufacturer: Japan Carlit)
PEL25: Compound represented by Chemical Formula 2 wherein R is an ethyl group, m is between about 0 and 1 and n is about 28 to 29 (manufacturer: Japan Carlit)
PEGEH: polyethyleneglycol bis (2-ethylhexanoate) (Additional moles of ethylene oxide unit: 9)
LiTFSi: lithium bis (trifluoromethanesulfonyl) imide
AA: Acetyl Acetone
Equivalence ratio 1: ratio of the hydroxyl group equivalent (OH) of a polymer and the isocyanate group equivalent (NCO) of a crosslinking agent (NCO / OH)
Equivalence ratio 2: Ratio of the isocyanate group equivalent (NCO) of a crosslinking agent with respect to the sum total of the hydroxyl group equivalent (OH1) of a polymer, and the hydroxyl group equivalent (OH2) of a compound of General formula (NCO / (OH1 + OH2)).

The results of evaluating the physical properties of the pressure-sensitive adhesive compositions of the Examples and Comparative Examples prepared above are summarized in Table 3 below.

Example Comparative example One 2 3 4 5 One 2 3 4 5 L-peel 4.5 73/18 5.5 7 5 3.5 7.0 7.5 4.0 5.2 H-peel 95 73 85 100 75 80 95 120 110 160 H / L 21 18 15 14 15 23 14 16 28 31 Peeling voltage 0.2 0.15 0.3 0.25 0.45 0.2 0.3 0.3 > 1.0 > 1.0 Pollutant A A A A A B B B A B L-peel: Low Peel Force (Unit: gf / 25mm)
H-peel: high speed peeling force (unit: gf / 25mm)
H / L: ratio of low speed and high speed peeling force
Stripping voltage unit: kV

Claims (17)

Alkyl (meth) acrylate which has a C1-C14 alkyl group;
As a first monomer included in a ratio of 0.1 to 20 parts by weight relative to 100 parts by weight of the alkyl (meth) acrylate, represented by the following formula (1), the number of carbons included in the alkylene group of A and B of the formula (1) 1 to A first monomer in the range of 3; And
As a second monomer included in a ratio of 0.1 to 5 parts by weight relative to 100 parts by weight of the alkyl (meth) acrylate, represented by the following formula (1), the number of carbons including the alkylene groups of A and B of the formula (1) 4 to Polymers of monomer mixtures comprising a second monomer within the range of 8;
0.1 to 3 parts by weight of the compound represented by the following formula (2) relative to 100 parts by weight of the polymer; And
3 to 15 parts by weight of isocyanate crosslinking agent based on 100 parts by weight of the polymer,
The equivalent of the isocyanate group of the isocyanate crosslinking agent is in the range of 1 to 2.3 equivalents per 1 equivalent of the hydroxy group included in the polymer, or the equivalent of the isocyanate group of the isocyanate crosslinking agent is the sum of the hydroxyl group of the polymer and the hydroxy group of the compound of formula 2 Pressure-sensitive adhesive composition in the range of 1.0 to 2.0 equivalents per equivalent:
[Formula 1]

In Formula 1, Q is hydrogen or an alkyl group, A and B are each independently an alkylene group, and n is a number in the range of 0 to 10:
[Formula 2]

In formula (2), R is a hydrogen atom or an alkyl group having 1 to 4 carbon atoms, n is a number in the range of 0 to 32, and m is a number in the range of 5 to 50. The pressure-sensitive adhesive composition according to claim 1, wherein the ratio (A / B) of the weight (A) of the first monomer and the weight (B) of the second monomer is in the range of 0.1 to 20. The pressure-sensitive adhesive composition of claim 1, wherein n is a number in the range of 5 to 30, and m is a number in the range of 10 to 40. delete delete The pressure-sensitive adhesive composition of claim 1, wherein the crosslinking agent is an aliphatic isocyanate crosslinking agent. The pressure-sensitive adhesive composition of claim 6, wherein the crosslinking agent comprises at least one selected from the group consisting of aliphatic cyclic isocyanate compounds and aliphatic acyclic isocyanate compounds. The isocyanate compound according to claim 7, wherein the aliphatic cyclic isocyanate compound is isoborone diisocyanate, methylene dicyclohexyl diisocyanate or cyclohexane diisocyanate; Dimers or trimers of the isocyanate compounds; Or a pressure-sensitive adhesive composition which is a reactant of the isocyanate compound and a polyol. 8. The compound according to claim 7, wherein the aliphatic acyclic isocyanate compound is an alkylene diisocyanate compound having 1 to 20 carbon atoms; Dimers or trimers of the isocyanate compounds; Or a pressure-sensitive adhesive composition which is a reactant of the isocyanate compound and a polyol. The pressure-sensitive adhesive composition of claim 1, further comprising 0.1 to 5 parts by weight of the ionic compound relative to 100 parts by weight of the polymer. According to claim 1, wherein the pressure-sensitive adhesive composition further comprises 0.05 to 5 parts by weight of the compound of formula 3 relative to 100 parts by weight of the polymer:
[Formula 3]

In Formula 3, M ₁ to M ₅ are each independently R ₁ -N, (R ₂ ) (R ₃ ) -C or (R ₄ ) (R ₅ ) -C, wherein R ₁ is a hydrogen atom, an alkyl group or An alkoxy group, R ₂ and R ₃ are each independently an alkyl group, R ₄ and R ₅ are each independently a hydrogen atom or an alkyl group, L is an alkylene group or an alkylidene group, P is an alkyl group or a substituent of the formula Wherein at least one of M ₂ to M ₄ in Formula 3 is R ₁ -N and M ₁ , M ₂ , M _{3 which is} present immediately adjacent to M ₂ , M _3, or M ₄ , which is R ₁ -N. , M ₄ or M ₅ is (R ₂ ) (R ₃ ) -C.):
[Formula 4]

In Formula 4, M ₆ to M ₁₀ are each independently R ₁ -N, (R ₂ ) (R ₃ ) -C or (R ₄ ) (R ₅ ) -C, wherein R ₁ is a hydrogen atom, an alkyl group or An alkoxy group, R ₂ and R ₃ are each independently an alkyl group, and R ₄ and R ₅ are each independently a hydrogen atom or an alkyl group, provided that at least one of M ₇ to M ₉ in Formula 4 is R ₁ -N And M ₆ , M ₇ , M ₈ , M ₉ or M ₁₀ present immediately adjacent to M ₇ , M ₈ or M ₉ is (R ₂ ) (R ₃ ) -C.) 12. The compound of claim 11, wherein in formula (3), R ₁ is a hydrogen atom, an alkyl group having 1 to 8 carbon atoms, an alkoxy group having 4 to 16 carbon atoms, R ₂ and R ₃ are each independently an alkyl group having 1 to 12 carbon atoms, and L The adhesive composition which is silver a C4-C12 alkylene group or a C2-C10 alkylidene group. 12. The compound of claim 11, wherein the compound of formula 3 is bis (1,2,2,6,6-pentamethyl-4-piperidyl) sebacate, methyl 1,2,2,6,6-pentamethyl-4 -Piperidyl sebacate, propanedioic acid 2-[[3,5-bis (1,1-dimethylethyl) -4-hydroxyphenyl] methyl] -2-butyl-1,3-bis (1,2 , 2,6,6-pentamethyl-4-piperidinyl) ester, bis (2,2,6,6-tetramethyl-4-piperidyl) sebacate or bis (1-octyloxy-2,2 , 6,6-tetramethyl-4-piperidinyl) sebacate. Surface protective base layer; And a pressure-sensitive adhesive layer formed on one or both surfaces of the base material layer and comprising the pressure-sensitive adhesive composition according to claim 1 in a crosslinked state. The optical element with which the protective film of Claim 14 is attached so that peeling is possible on the surface. The optical element of Claim 15 whose surface energy of the surface with a protective film is 30 mN / m or less. A display device comprising the optical element of claim 15.