KR20140142874A

KR20140142874A - Pressure sensitive adhesive composition

Info

Publication number: KR20140142874A
Application number: KR1020130064549A
Authority: KR
Inventors: 김기영; 윤성수; 배정식
Original assignee: 주식회사 엘지화학
Priority date: 2013-06-05
Filing date: 2013-06-05
Publication date: 2014-12-15

Abstract

The present application relates to a pressure-sensitive adhesive composition, a protective film, an optical element and a display device. The pressure-sensitive adhesive composition of the present application has excellent storage stability, exhibits a suitable low-speed and high-speed peeling force after the crosslinked structure is formed, and has excellent balance between the two. 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 high-speed peeling, is advantageous in terms of high-speed processing, and exhibits excellent antistatic properties in the process .

Description

[0001] PRESSURE SENSITIVE ADHESIVE COMPOSITION [0002]

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

A protective film may be used to prevent dust, dirt, or the like from adhering to the optical element such as a polarizing plate, other plastic products, household appliances, automobiles, or the like. The protective film is required to have an appropriate peeling force and antistatic property.

For example, when a protective film is peeled at a high speed for use of a product or for assembling another product, it is required that the peel force (hereinafter, referred to as "high peel force") be 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 rate may be relatively high to exhibit an appropriate protective function.

In addition, foreign matter such as dust may be sucked due to static electricity generated mainly at the time of peeling off the protective film, and in the case of electronic products, electrostatic destruction or malfunction of the device may be caused. Particularly, in recent years, due to the spread of computers and the multifunctionality of liquid crystal TVs and mobile phones, components are integrated, and problems caused by static electricity are becoming more and more evident.

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 is an attempt to suppress the generation of static electricity by blending an ethylene oxide-modified dioctyl phthalate plasticizer with a pressure-sensitive adhesive. In Patent Document 2, an organic salt is added to a pressure-sensitive adhesive, and in Patent Document 3, a metal salt and a chelating agent are mixed in a pressure-sensitive adhesive. However, according to the above methods, it is difficult to prevent the occurrence of contamination of the adhesive component by transfer to the protected product or to suppress the static electricity generated at the initial stage, and particularly, the low-speed peeling force which is important for the protective function is excessively low.

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

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

Exemplary pressure sensitive adhesive compositions may include polymers and light stabilizers. The polymer in the pressure-sensitive adhesive composition may be a polymer having a crosslinking point, and in such a case, the polymer may react with a crosslinking agent which may be further contained in the pressure-sensitive adhesive composition to realize a crosslinked structure.

As the polymer, various kinds known to be usable in the production of the pressure-sensitive adhesive can be used. The polymer may comprise, for example, polymerized units derived from monomers comprising alkylene oxide chains. As used herein, the term monomers means all kinds of compounds capable of forming a polymer through a polymerization reaction, and a polymer containing polymerized units derived from certain monomers may mean a polymer formed by polymerizing any of the above monomers .

As the monomer having an alkylene oxide chain, for example, a compound represented by the following formula (1) can be exemplified.

[Chemical Formula 1]

In Formula (1), Q is hydrogen or an alkyl group, U is an alkylene group or an alkylidene group, Z is an alkyl group or an aryl group, and m is an arbitrary number, for example, 1 to 20.

When two or more [-U-O-] units are present in the formula (1), the number of carbon atoms of the U in the unit may be the same or different.

In formula (1), m may be, for example, 1 to 16, 1 to 12, 4 to 16, 4 to 12, 4 to 10 or 4 to 8. Within this range, it is possible to maintain the polymerization efficiency and the crystallinity of the polymer in an appropriate range during production of the polymer, and to give the pressure-sensitive adhesive an appropriate conductivity.

As used herein, the term alkyl group may mean an alkyl 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, unless otherwise specified. The alkyl group may be straight-chain, branched or cyclic. The alkyl group may be substituted by one or more substituents, or may be unsubstituted.

As used herein, unless otherwise specified, the term "alkylene group" or "alkylidene group" means 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, have. The alkylene group or alkylidene group may be linear, branched or cyclic. The alkylene or alkylidene group may be optionally substituted by one or more substituents.

In another embodiment, Q in formula (1) may be an alkyl group, for example, an alkyl group having 1 to 8 carbon atoms or 1 to 4 carbon atoms. When Q is an alkyl group, for example, it may be advantageous that the protective film is easily removed without residue or unevenness on the adherend when the pressure-sensitive adhesive composition is applied to a protective film or the like.

As used herein, the term aryl group, unless otherwise specified, includes a benzene ring, or two or more benzene rings may be connected, or two or more benzene rings may share one or more carbon atoms, May refer to a monovalent residue derived from a compound or a derivative thereof having a structure represented by the following formula: The aryl group may be, for example, an aryl group having 6 to 25 carbon atoms, 6 to 22 carbon atoms, 6 to 16 carbon atoms, or 6 to 13 carbon atoms. Examples of the aryl group include a phenyl group, a phenylethyl group, a phenylpropyl group, a benzyl group, a tolyl group, a xylyl group and a naphthyl group.

Examples of the substituent which may be substituted in the specific functional group, for example, the alkyl group, the alkylidene group or the alkylene group in the present specification include an alkyl group, an alkoxy group, an alkenyl group, an epoxy group, a cyano group, a carboxyl group, An acryloyloxy group, a methacryloyloxy group or an aryl group, but the present invention is not limited thereto.

Examples of the compound represented by the formula (1) include alkoxy dialkylene glycol (meth) acrylic acid ester, alkoxy trialkylene glycol (meth) acrylic acid ester, alkoxy tetraalkylene glycol (meth) acrylic acid ester, aryloxy dialkylene glycol (Meth) acrylic acid esters, aryloxytetraalkylene glycol (meth) acrylic acid esters, and polyalkylene glycol monoalkyl ether (meth) acrylic acid esters. But is not limited to.

Examples of the alkoxy include alkoxy having 1 to 20 carbon atoms, 1 to 16 carbon atoms, 1 to 12 carbon atoms and 1 to 4 carbon atoms, and specifically, a methoxy group or an ethoxy group can be exemplified .

Examples of the alkylene glycol include alkylene glycols having 1 to 20 carbon atoms, 1 to 16 carbon atoms, 1 to 12 carbon atoms and 1 to 4 carbon atoms, and examples thereof include ethylene glycol and propylene glycol In the above, aryloxy is exemplified by aryloxy having 6 to 24 carbon atoms or 6 to 12 carbon atoms such as phenoxy.

The polymer may further comprise polymerized units derived from a monomer having a hydroxy group. The polymerized unit may provide a hydroxy group to the polymer.

As the monomer having a hydroxy group, for example, a monomer represented by the following formula (2) can be mentioned.

(2)

In formula (2), Q is hydrogen or an alkyl group, A and B are each independently an alkylene group or an alkylidene group, and n is an arbitrary number, for example, a number of 0 to 10.

When two or more [-O-B-] units are present in the general formula (2), the number of carbon atoms of B in the unit may be the same or different

In formula (2), A and B may be, for example, each independently an alkylene group which is linear.

Examples of the compound of formula (2) include 2-hydroxyethyl (meth) acrylate, 2-hydroxypropyl (meth) acrylate, 4-hydroxybutyl (meth) acrylate, 6-hydroxyhexyl (Meth) acrylate, 2-hydroxyethyleneglycol (meth) acrylate or 2-hydroxypropyleneglycol (meth) acrylate, but are not limited thereto.

The polymer may include polymerized units derived from 1 to 20 parts by weight of the monomer of formula (1) and 1 to 40 parts by weight of the monomer of formula (2). As used herein, the term " weight portion " means the ratio of the weight between the components unless otherwise specified. Accordingly, the polymerized units derived from 1 to 20 parts by weight of the monomer of formula (1) and the polymerized units derived from 1 to 40 parts by weight of the compound of formula (2) as described above include, for example, The monomers of the formula 1 and the monomers of the formula 2 are included so that the ratio (A: B) of the weight (A) of the monomers of formula (1) to the weight (B) of the monomers of formula Lt; RTI ID = 0.0 > of a < / RTI >

In another example, the polymerized units derived from the monomers of formula (1) contained in the polymer comprise from about 1 part by weight to 20 parts by weight, from about 1 part by weight to 18 parts by weight, or from about 2 parts by weight to 18 parts by weight, It may be derived. Also, the polymerized units derived from the monomer of Formula 2 contained in the polymer may be present in an amount of from about 2 parts by weight to about 40 parts by weight, from about 10 parts by weight to about 40 parts by weight, from about 10 parts by weight to 35 parts by weight, To 30 parts by weight or from about 10 parts by weight to 25 parts by weight of the monomer of formula (2). It is possible to provide a pressure-sensitive adhesive exhibiting an appropriate antistatic property under such a ratio and exhibiting a balance of appropriate high-speed and low-speed peeling force without leaving a contaminant at the time of peeling.

In one example, as the monomer having a hydroxy group, two types of monomers having different carbon numbers present in the side chain may be used.

For example, the polymer may be derived from a monomer (hereinafter referred to as a first monomer) satisfying the following condition 1 and a monomer represented by the above formula 2 and satisfying the following condition 2 (hereinafter referred to as a second monomer) Lt; RTI ID = 0.0 > polymerized < / RTI >

[Condition 1]

1 to 3 = a + bxn

[Condition 2]

4? A + b? N

In Conditions 1 and 2, a is the number of carbon atoms of the alkylene group or alkylidene group of A in Chemical Formula 2, b is the number of carbon atoms of the alkylene group or alkylidene group of B, and n is the number same.

In the case of the second monomer, the number calculated by the formula " a + b x n " is for example 4 to 20, 4 to 16, 4 to 12, 4 to 8 or 4 To six.

When the polymer contains the first and second monomers, the ratio of the monomers is not particularly limited. For example, the polymer may be used in an amount of 1 to 30 parts by weight of the first monomer and 1 to 10 parts by weight of the second monomer And may include polymerized units derived from the moiety. In another example, the polymer comprises polymerized units derived from about 1 to about 25 parts by weight or about 1 to about 20 parts by weight of the first monomer and about 1 to about 8 parts by weight or about 1 to about 8 parts by weight of the second monomer, To 5 parts by weight of the polymerized units. It is possible to provide a pressure-sensitive adhesive which exhibits an appropriate antistatic property within such a ratio and exhibits a balance of appropriate high-speed and low-speed peeling force without leaving a contaminant at the time of peeling.

The polymer may further comprise polymerized units derived from (meth) acrylic acid ester monomers, for example, alkyl (meth) acrylates.

As the alkyl (meth) acrylate, for example, an alkyl (meth) acrylate having an alkyl group having 1 to 14 carbon atoms may be used in consideration of the cohesive force of the pressure-sensitive adhesive, the glass transition temperature, or the tackiness. Examples of such monomers include methyl (meth) acrylate, ethyl (meth) acrylate, n-propyl (meth) acrylate, isopropyl (meth) acrylate, (Meth) acrylate, n-octyl (meth) acrylate, isooctyl (meth) acrylate, sec-butyl (Meth) acrylate, isononyl (meth) acrylate, lauryl (meth) acrylate and tetradecyl (meth) acrylate. Of these, .

The polymerized unit derived from the (meth) acrylic acid ester monomer may be derived from, for example, 67 parts by weight to 97 parts by weight of the (meth) acrylic acid ester monomer. For example, the ratio (A: B: C) of the weight (A) of the monomer of the formula (1), the weight of the monomer of the formula (2) and the weight of the (meth) ) Is " 1 to 20: 1 to 40:67 to 97 ", the polymer may be formed from a mixture of monomers containing the respective monomers. However, the weight ratio may be changed, for example, in consideration of the specific kind of each monomer and the like, if necessary.

The polymer can be a known monomer used in the production of a polymer of a pressure-sensitive adhesive, such as (meth) acrylic acid, 2- (meth) acryloyloxyacetic acid, 3- (meth) acryloyloxypropyl , Carboxyl group-containing monomers such as 4- (meth) acryloyloxybutyric acid, acrylic acid dimer, 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 a monomer having a nitrogen atom such as (meth) acrylamide, N-vinylpyrrolidone or N-vinylcaprolactam, And may further include a radically polymerizable monomer such as a monomer or styrene. These monomers may be polymerized and included in the polymer, and may be included in the polymer in a ratio of, for example, about 20 parts by weight or less.

The polymer may be obtained by selecting a desired monomer among the above-described monomers and then subjecting the mixture of the monomers having the desired proportions of the selected monomers to a solution polymerization, a photo polymerization, a bulk polymerization, suspension polymerization, or emulsion polymerization, for example.

The pressure-sensitive adhesive composition may include a light stabilizer, for example, a light stabilizer such as a hindered amine compound. Such a light stabilizer is not agglomerated even when the pressure-sensitive adhesive is left under high temperature conditions, for example, so that the concentration of the antistatic agent to be described later in the agglomerated cluster is not increased, and the alkylene oxide chain Can be decomposed by heat to generate radicals, or the monomer having a hydroxyl group can be prevented from causing a condensation reaction, and the storage stability of the pressure-sensitive adhesive composition can be greatly improved.

As the light stabilizer, for example, a compound represented by the following general formula (3) can be exemplified.

(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 , and, in said R ¹ is a hydrogen atom, an alkyl group or alkoxy group, R ² and R ³ are each and independently selected from 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 (4) 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 in the ^{(R 2) (R 3)} -C.

[Chemical 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, 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 the formulas (3) and 4 M ₁ to M ₁₀ is ^{R 1 -N, (R 2)} (R 3) -C or ^{(R 4) (R 5)} -C called it, the nitrogen of said M ₁ to M ₁₀ position ^May mean a form in which an atom (N) or a carbon atom (C) is present and a substituent such as R ¹ to R ⁵ is bonded to the nitrogen atom or the carbon atom.

In the formula (4)

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

L, which is an alkylene group or an alkylidene group in the general formula (3), may be substituted or unsubstituted, if necessary. For example, L may be substituted by an aryl group, and examples of the aryl group include 3,5-bis (1,1-dimethylethyl) -4-hydroxyphenyl group and the like, It is not.

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

Examples of the compound of Formula 3 include bis (1,2,2,6,6-pentamethyl-4 (2,2,2,6,6-pentamethyl-4-piperidyl) -piperidyl sebacate, methyl 1,2,2,6,6-pentamethyl-4-piperidyl sebacate, propanedioic acid, Methyl] -2-butyl-1,3-bis (1,2,2,6,6-pentamethyl-pyrimidin- Propanedioic acid, 2 - [[3,5-bis (1,1-dimethylethyl) -4-hydroxyphenyl] methyl] -2-butyl-1,3-bis , 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, and the like, but are not limited thereto.

The compound of Formula 3 may be used in an amount of, for example, 0.01 to 10 parts by weight, 0.05 to 10 parts by weight, 0.05 to 8 parts by weight, 0.05 to 6 parts by weight, or 0.05 to 5 parts by weight, To 5 parts by weight of the pressure-sensitive adhesive composition. It is possible to provide a pressure-sensitive adhesive composition which effectively prevents generation of radicals due to decomposition of the alkylene oxide chain and condensation of a hydroxyl group-containing monomer under such a ratio, and is excellent in storage stability.

The pressure-sensitive adhesive composition may further include a crosslinking agent, which may react with the crosslinking point of the polymer to realize a crosslinked structure.

As the crosslinking agent, for example, an aliphatic isocyanate crosslinking agent can be used. When such a crosslinking agent has a crosslinking structure with the polymer, that is, a polymer containing a monomer having two or more hydroxyl groups, a pressure-sensitive adhesive having necessary antistatic properties together with a suitable low-speed and high-speed peeling force can be realized. For example, as the crosslinking agent, a crosslinking agent comprising an aliphatic cyclic isocyanate compound and / or an aliphatic acyclic isocyanate compound can be used. The term aliphatic cyclic isocyanate compound as used herein means an isocyanate compound containing a cyclic structure and having a cyclic structure in which the structure does not correspond to an aromatic ring. The aliphatic acyclic isocyanate compound may be, for example, an aliphatic linear or branched May mean a branched isocyanate compound. Examples of the aliphatic cyclic isocyanate compound include isocyanate compounds such as isophorone diisocyanate or methylene dicyclohexyl diisocyanate or cyclohexane diisocyanate, A derivative such as a dimer or a trimer or a reaction product of any of the above with a polyol (ex. Trimethylol propane) can be exemplified. As the aliphatic acyclic isocyanate compound, there may be mentioned a compound having a carbon number of 1, such as hexamethylene diisocyanate An alkylene diisocyanate compound having from 1 to 20 carbon atoms, from 1 to 12 carbon atoms, or from 1 to 8 carbon atoms, a derivative thereof such as a dimer or a trimer thereof, or any one of the above and a polyol (e.g., trimethylol Propane) And the like, but the present invention is not limited thereto.

When 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 needed. Generally, from 1 part by weight to 500 parts by weight or from 20 parts by weight to 300 parts by weight of an 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, and examples thereof include MHG-80B and Duranate P manufactured by Asahi, or NZ-1 manufactured by BAYER .

As the crosslinking agent, ethylene glycol diglycidyl ether, triglycidyl ether, trimethylol propane triglycidyl ether, N, N, N ', N'-tetraglycidyl ethylenediamine or glycerin Epoxy cross-linking agents such as diglycidyl ether and the like; Bis (1-aziridine carboxamide), N, N'-diphenylmethane-4,4'-bis (1-aziridine carboxamide), triethylene melamine Iron, zinc, tin, titanium, antimony, magnesium, and / or vanadium, such as bis (isoproparyl) -1- (2-methyl aziridine), or tri-1-aziridinyl phosphine oxide, Can be used together with a known crosslinking agent such as a metal chelate crosslinking agent, which is a compound coordinated to acetyl acetone, acetyl acetate or the like.

The pressure-sensitive adhesive composition may include 0.01 to 10 parts by weight or 0.01 to 5 parts by weight of a crosslinking agent based on 100 parts by weight of the polymer. In such a range, an appropriate crosslinking structure is realized, and the low speed and high speed peeling force of the pressure sensitive adhesive can be adjusted to a desired range.

The pressure-sensitive adhesive composition may further comprise an antistatic agent. As the antistatic agent, for example, an ionic compound may be used.

As the ionic compound, for example, a metal salt may be used. The metal salt may include, for example, an alkali metal cation or an alkaline earth metal cation. Cations, the lithium ions (Li ^+), sodium ion (Na ^+), potassium ion (K ^+), rubidium ions (Rb ^+), cesium ion (Cs ^+), beryllium ion (Be ² ^+), magnesium ion ( Mg ² ^+), calcium ions (Ca ² ^+), strontium ion (Sr ² ⁺⁾ and barium ion (Ba ² ⁺⁾ there is iljong or two kinds or more of the like can be illustrated, for example, a lithium ion, a sodium ion, Potassium ion, magnesium ion, calcium ion and barium ion, or ion 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-), carboxymethyl sulfonate _{(COOH (C 6 H 4)} SO 3 -), sulfonate as a triple (CF ₃ SO ₂ ^-), benzo carbonate _{^{(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 ^- ), and the like.

In another example, the anion may be an anion or bifluorosulfonylimide represented by the following formula (5), or the like.

[Chemical Formula 5]

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

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, and when Y is sulfur, m is 2, n is 2 when X is nitrogen, and n is 3 when X is carbon.

The anion or bis (fluorosulfonyl) imide of formula (5) exhibits high electronegativity due to the perfluoroalkyl group (R _f ) or the fluorine group and also forms a weak bond with the cation, including a unique resonance structure And at the same time has hydrophobicity. Therefore, the ionic compound exhibits excellent compatibility with other components of the composition such as a polymer, and can give a high antistatic property even in a small amount.

R _f in 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, wherein the perfluoroalkyl group may be a straight chain, And may have a cyclic structure. The anion of formula (5) may be a sulfonylimide-based, sulfonylimide-based, carbonylimide-based or carbonylimide-based anion, and specifically includes tris trifluoromethanesulfonylmethide, bistrifluoromethanesulfonyl A perfluorobutanesulfonylimide, bispentafluoroethanesulfonylimide, tris trifluoromethanecarbonylmide, bis perfluorobutanecarbonylimide or bispentafluoroethanecarbonyl, bispentafluoroethanesulfonylimide, bis Imide, etc., or a mixture of two or more species.

Examples of the ionic compound include N, N-dimethyl N-propylammonium, N, N, N-trimethyl-N-propylammonium, N-methyl- N, N, N-trihexylammonium, N-methyl-N, N, N-trihexylammonium, N-ethyl- Quaternary ammonium such as N, N, N-trioctylammonium or N-ethyl-N, N, N-trioctylammonium, phosphonium, pyridinium, imidazolium, An organic salt containing pyrolidinium or piperidinium together with the anion component may be used and, if necessary, the metal salt and the organic salt may be used in combination.

The content of the ionic compound in the pressure-sensitive adhesive composition is not particularly limited and may be, for example, 0.01 to 5 parts by weight relative to 100 parts by weight of the polymer. The ratio of the ionic compound can be changed in consideration of the desired antistatic property and compatibility between the components.

The pressure-sensitive adhesive composition may further include a silane coupling agent. Examples of the coupling agent include gamma-glycidoxypropyltriethoxysilane, gamma-glycidoxypropyltrimethoxysilane, gamma-glycidoxypropylmethyldiethoxysilane, gamma-glycidoxypropyltriethoxysilane , 3-mercaptopropyltrimethoxysilane, vinyltrimethoxysilane, vinyltriethoxysilane, gamma-methacryloxypropyltrimethoxysilane, gamma-methacryloxypropyltriethoxysilane, gamma-aminopropyltri But are not limited to, methoxy silane, gamma-aminopropyl triethoxy silane, 3-isocyanatopropyl triethoxy silane, gamma-acetoacetate propyl trimethoxysilane, gamma-acetoacetate propyl triethoxy silane, Trimethoxysilane, beta-cyanoacetyltriethoxysilane, acetoxyacetotrimethoxysilane, and mixtures of one or more of the above can be used. . For example, as the silane coupling agent, it may be appropriate to use a silane coupling agent having an acetoacetate group or a beta-cyanoacetyl group. The silane coupling agent may be contained in the adhesive composition in an amount of 0.01 to 5 parts by weight, or 0.01 to 1 part by weight based on 100 parts by weight of the polymer. An appropriate adhesive force increasing effect and endurance reliability can be ensured within the above range.

The pressure-sensitive adhesive composition may further include a tackifier in view of control of the tack performance. Examples of the tackifier include a hydrocarbon resin or a hydrogenated product thereof, a rosin resin or a hydrogenated product thereof, a rosin ester resin or a hydrogenated product thereof, a terpene resin or a hydrogenated product thereof, a terpene phenol resin or a hydrogenated product thereof, Ester resins and the like, or mixtures of two or more thereof. The tackifier may be contained in the composition in an amount of 1 part by weight to 100 parts by weight based on 100 parts by weight of the copolymer. It is possible to secure a suitable addition effect and a commercial and cohesive force improving effect in the above content range.

The pressure-sensitive adhesive composition may also contain a coordinating compound capable of forming a coordination bond with the antistatic agent, a photoinitiator, a multifunctional acrylate, an epoxy resin, a crosslinking agent, a UV stabilizer, an antioxidant, A colorant, a reinforcing agent, a filler, a defoaming agent, a surfactant, and a plasticizer.

The pressure-sensitive adhesive composition has a low peel strength of about 1 gf / 25 mm to 40 gf / 25 mm, 1 gf / 25 mm to 30 gf / 25 mm for an adherend having a surface energy of 30 mN / m or less, 25 mm to 20 gf / 25 mm or 1 gf / 25 mm to 10 gf / 25 mm, and the high-speed peeling force may be about 10 gf / 25 mm to 150 gf / 25 mm or 10 gf / 25 mm to 100 gf / 25 mm.

The term low-speed peeling force is, for example, the peeling force measured at a peeling angle of 180 degrees and a peeling speed of 0.3 m / min. The high-speed peeling force was measured at a peeling angle of 180 degrees and a peeling speed of 30 m / min It can be peeling force.

Specifically, each of the peel strengths was measured by attaching a pressure-sensitive adhesive composition having a crosslinked structure to an adherend having a surface energy of 30 mN / m or less, holding the layer at 23 ° C and 65% relative humidity for 24 hours, And may be one measured at each peeling angle and peeling speed. A specific method of measuring each of the peeling forces 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 can be applied. For example, the contact angle of an adherend may be measured, the surface energy may be determined therefrom, or the surface energy may be measured using a known surface energy measuring device. The surface energy of the adherend may be, for example, about 10 m / N / m to 30 mN / m.

The pressure-sensitive adhesive composition may also have a ratio (H / L) of the high-speed peeling force (H) to the low-speed peeling force (L) of 1 to 20, 5 to 20, or 7 to 15.

The pressure-sensitive adhesive composition is also excellent in peeling electrification voltage, which is generated when the adherend, i.e., an adherend having a surface energy of 30 mN / m or less is peeled off at a peeling angle of 180 degrees and a peeling speed of 40 m / Can be 0.7 kV or less. The method of measuring the peeling electrification voltage is described in the following examples.

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

The present application is also directed to a pressure sensitive adhesive sheet. The adhesive sheet may be, for example, a protective film, specifically a protective film for an optical element.

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

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

The pressure-sensitive adhesive composition exhibits relatively high low-speed peeling force and relatively low high-speed peeling force after the crosslinked structure is implemented, and excellent balance between the peel strength and excellent durability reliability, workability, transparency and antistatic property. Thus, the protective film is used for protecting the surface of an optical element such as a polarizing plate, a retardation plate, an optical compensation film, a reflection sheet and a brightness enhancement film used for various optical devices or parts, display devices or parts such as LCD , But the use of the protective film is not limited to the use of the protective film.

As the surface protective base film, a general film or sheet known in this field can be used. For example, a polyester film such as polyethylene terephthalate or polybutylene terephthalate, a polytetrafluoroethylene film, a polyethylene film, a polypropylene film, a polybutene film, a polybutadiene film, a poly (vinyl chloride) film or a polyimide film And the like. Such a film may be composed of a single layer, or two or more layers may be laminated, and in some cases, a functional layer such as an antifouling layer or an antistatic layer may further be included. From the viewpoint of improving the adhesion of the substrate, a surface treatment such as a primer treatment may be performed on one surface or both surfaces of the substrate.

The thickness of the base film may be suitably selected depending on the application and is not particularly limited, and may be generally formed to a thickness of 5 to 500 탆 or 10 to 100 탆.

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 m to 100 m or 5 m to 50 m.

The method for forming the pressure-sensitive adhesive layer is not particularly limited, and for example, a pressure-sensitive adhesive composition or a coating solution prepared therefrom may be coated on a base film or the like by a conventional means such as a bar coater and cured, A method of coating on the surface of the base material and curing the base material, and transferring the base material film onto the base material film.

The process of forming the pressure-sensitive adhesive layer is preferably performed after sufficiently removing the bubble-inducing component such as the volatile component or the reaction residue in the pressure-sensitive adhesive composition or the coating liquid. Accordingly, the crosslinking density or the molecular weight of the pressure-sensitive adhesive is too low to lower the elastic modulus, and bubbles existing between the glass plate and the pressure-sensitive adhesive layer at high temperature are increased to form scattering bodies therein.

Also, the method of curing the pressure-sensitive adhesive composition in the above process is not particularly limited. For example, the polymer and the crosslinking agent contained in the composition may be subjected to an appropriate aging process to react them, or the activation of a photoinitiator For example, ultraviolet irradiation or the like.

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

[Equation 1]

Gel content = B / A x 100

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

The present application is also directed to optical elements. An exemplary optical element may include an optical element and the adhesive sheet attached to the 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, so that the optical element can be protected by the surface-protecting base film.

As the optical element included in the optical element, for example, a polarizer, a polarizing plate, a polarizer protective film, a retardation layer or a viewing angle compensation layer can be exemplified.

As the polarizer, for example, general types known in the art such as polyvinyl alcohol polarizers and the like can be employed without limitation.

A 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 and oriented on a polyvinyl alcohol-based resin film. The polyvinyl alcohol-based resin constituting the polarizer can be obtained by, for example, gelling a polyvinyl acetate-based resin. In this case, the polyvinyl acetate-based resin that can be used may include not only homopolymers of vinyl acetate but also copolymers of vinyl acetate and other monomers copolymerizable therewith. Examples of the monomer copolymerizable with vinyl acetate include monomers such as unsaturated carboxylic acids, olefins, vinyl ethers, unsaturated sulfonic acids, and acrylamides having an ammonium group, or a mixture of two or more thereof. no. The degree of gelation of the polyvinyl alcohol-based resin may be generally from 85 mol% to 100 mol%, preferably 98 mol% or more. The polyvinyl alcohol resin may be further modified. For example, polyvinyl formal or polyvinyl acetal modified with aldehydes may be used. 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.

A polyvinyl alcohol-based resin may be formed and used as the original film of the polarizer. The method of forming the polyvinyl alcohol-based resin is not particularly limited, and a general method known in this field can be used. The thickness of the original film formed of a polyvinyl alcohol-based resin is not particularly limited, and can be suitably controlled within a range of, for example, 1 m to 150 m. The thickness of the original film can be controlled to 10 mu m or more in consideration of easiness of drawing and the like. The polarizer is formed by a process of stretching a polyvinyl alcohol-based resin film as described above (e.g., uniaxial stretching), dyeing a polyvinyl alcohol-based resin film with a dichroic dye and adsorbing the dichroic dye, A process of treating a polyvinyl alcohol resin film with a boric acid aqueous solution and a process of washing with a boric acid aqueous solution after washing. As the dichroic dye, iodine or dichroic organic dyes may be used.

The polarizer may include, for example, the polarizer; And other optical films attached to one side or both sides of the polarizer. Examples of the other optical films include the above-described polarizer protective film, retardation layer, viewing angle compensation layer, antiglare layer, and the like.

The polarizer protective film is a protective film for a polarizer in a concept distinct from a protective film containing the pressure-sensitive adhesive layer. As the polarizer protective film, for example, a cellulose-based film such as triacetylcellulose; Acrylic film; Polyester-based films such as polycarbonate film or polyethylene terephthalate film; Polyethersulfone-based films; And a protective film composed of a polyethylene film, a polypropylene film, or a polyolefin film such as a polyolefin film having a cyclo or norbornene structure or an ethylene propylene copolymer, or the like. The thickness of the protective film is also not particularly limited, and can be formed in a usual thickness.

In the optical element, a surface treatment layer may be present on the surface of the optical element protected by the protective film. The surface treatment layer may have a surface energy of 30 mN / m or less, for example. That is, a surface treatment layer having a surface energy of 30 mN / m or less is formed on a surface of an 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 .

The surface treatment layer may be a low reflection layer such as an anti-glare layer or an anti-reflection (AR) layer or a low reflection (LR) layer such as a hard layer, an anti-glare layer or a semi- Can be illustrated.

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

The high hardness layer may be, for example, a resin layer having a high hardness. The resin layer may include, for example, a room temperature curing type, a moisture curing type, a thermosetting type, or an active energy ray curing type 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. The term " cured state " in the description of the hardened layer means a case where the components contained in each of the resin compositions are converted into a hard state through a cross-linking reaction or a polymerization reaction. The above-mentioned room temperature curing type, moisture curing type, thermosetting type or active energy ray curable type resin composition can be prepared by heating the cured state at room temperature or by heating in the presence of appropriate humidity or irradiation of active energy rays &Lt; / RTI > composition.

In this field, various resin compositions are known which can satisfy the pencil hardness in the above-mentioned range in a cured state, and an average person 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 or a polyester compound as a main component. In the above, the "compound" may be a monomeric, oligomeric or polymeric compound.

In one example, 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 as the resin composition.

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

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

Examples of the reactive diluting monomer which can be contained in the active energy ray-curable acrylic composition include monomers having one or more active energy ray-curable functional groups such as an acryloyl group or a methacryloyl group . As the reactive diluting monomer, for example, the above (meth) acrylic acid ester monomers, multifunctional acrylates, and the like can be used.

The selection of the above-mentioned components for forming the active energy ray-curable acrylic composition, the blending ratio of the selected components and the like are not particularly limited and can be adjusted in consideration of the hardness and other physical properties of the desired resin layer.

As the anti-glare layer such as the AG layer or the SG layer, for example, a resin layer in which an uneven surface is formed or a resin layer containing particles, wherein the resin is a particle layer having a refractive index different from that of the resin layer .

As the resin layer, for example, a resin layer used for forming the high hardness layer may be used. In the case of forming the anti-glare layer, it is not necessary to adjust the components of the resin composition so that the resin layer necessarily exhibits high hardness, but a resin layer may be formed so as to exhibit high hardness.

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 a coating layer of the resin composition is brought into contact with a metal mold having a desired concavo-convex structure, or particles having a particle diameter appropriate for the resin composition may be blended, have.

The anti-glare layer may also be formed using particles having different refractive indices from the resin layer.

In one example, the difference in refractive index between the particles and the resin layer may be 0.03 or less or 0.02 to 0.2, for example. If the difference in refractive index is too small, it is difficult to cause haze. On the contrary, if the refractive index difference is excessively large, scattering in the resin layer occurs a lot and haze increases, but deterioration of light transmittance or contrast characteristics may be induced. And appropriate particles can be selected.

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, as the particles, particles having irregularities on the surface can be used. Such particles may have a mean surface roughness (Rz) of, for example, 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 between the irregularities 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 and in 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, barium sulfate, Examples of the organic particles include crosslinked or non-crosslinked particles 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, It is not.

The concavo-convex structure or the content of the particles formed on the resin layer is not particularly limited. The shape of the concave-convex structure or the content of the particles may be controlled such that the haze of the AG layer is about 5% to 15%, 7% to 13%, or about 10% And in the case of the SG layer, the haze can be adjusted to be about 1% to 3%. The haze can be measured according to the manufacturer's manual using a hazemeter such as HR-100 or HM-150 of Sephiroth Co.,

A low reflection layer such as an AR layer or an LR layer can be formed by coating a low refractive material. A low refractive index material capable of forming a low reflection layer is variously known and can be suitably selected and used for the optical element. The low reflection layer can be formed to have a reflectance of about 1% or less through coating of a low refractive material.

The formation of the surface treatment layer may be carried out in the manner described in Korean Patent Publication Nos. 2007-0101001, 2011-0095464, 2011-0095004, 2011-0095820, 2000-0019116, 2000-0009647, 2000 -0018983, 2003-0068335, 2002-0066505, 2002-0008267, 2001-0111362, 2004-0083916, 2004-0085484, 2008-0005722, 2008-0063107 A material known in JP-A-2008-0101801 or JP-A-2009-0049557 can also be used.

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

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

The type of the liquid crystal panel included in the liquid crystal display device is not particularly limited. For example, the present invention is not limited to the type, but various passive matrix methods including TN (Twisted Neumatic) type, STN (Super Twisted Neumatic) type, F (ferroelectric) type and PD (polymer dispersed LCD) type; Various active matrix systems including two-terminal and three-terminal; Any known liquid crystal panel including a horizontal mode (IPS mode) panel and a vertical mode (VA mode) panel can be applied. The types of other structures included in the liquid crystal display device and the manufacturing method thereof are also not particularly limited, and general structures in this field can be employed without any limitations.

The pressure-sensitive adhesive composition of the present application has excellent storage stability, exhibits a suitable low-speed and high-speed peeling force after the crosslinked structure is formed, and has excellent balance between the two. 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 high-speed peeling, is advantageous in terms of high-speed processing, and exhibits excellent antistatic properties in the process .

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 copolymer solids

The solid content of the acrylic copolymer was measured by placing the prepared polymer solution in a disposable aluminum dish and measuring the weight, and then calculating the weight per unit weight before and after drying in a laboratory convection oven at a temperature of about 120 ° C for about 3 hours.

2. Measurement of viscosity

The polymerized acrylic copolymer was weighed into a 250-mL glass bottle at a weight of about 200 g and placed in a thermostatic chamber maintained at 23 DEG C for 30 minutes. When the temperature reached equilibrium, a Brookfield viscometer (DV- II +)) was used to measure the viscosity in the RPM section to maintain the confidence interval torque.

3. Low speed Exfoliation Measure

The pressure-sensitive adhesive sheets prepared in Examples and Comparative Examples were attached to the anti-glare layer of the polarizing plate on which the anti-glare layer was formed, using a roller of 2 Kg according to JIS Z 0237. Thereafter, the sample was stored at a temperature of 23 DEG C and a relative humidity of 65% for 24 hours, and then cut to a length of 25 mm and a length of 120 mm. Thereafter, the specimen was fixed to the glass substrate, and the peeling force was measured using a tensile tester while peeling the adhesive sheet from the antiglare layer in the transverse direction at a peeling angle of 180 degrees and a peeling rate of 0.3 m / min. The peeling force was measured for two identical specimens and the average value was adopted.

4. High speed Exfoliation Measure

The pressure-sensitive adhesive sheets prepared in Examples and Comparative Examples were attached to the anti-glare layer of the polarizing plate on which the anti-glare layer was formed, using a roller of 2 Kg according to JIS Z 0237. Thereafter, after being stored at a temperature of 23 DEG C and a relative humidity of 65% for 24 hours, the specimen was cut by cutting to a length of 25 mm and a length of 250 mm. Thereafter, the specimen was fixed to the glass substrate, and the peeling force was measured while peeling the adhesive sheet from the anti-glare layer in the transverse direction at a peeling angle of 180 degrees and a peeling speed of 30 m / min using a tensile tester. The peeling force was measured for two identical specimens and the average value was adopted.

5. Peeling Voltage ( ESD )

The specimens were the same as those used for low speed and high speed peel force measurements, with a length of about 22 cm and a length of about 25 cm. Subsequently, the specimen was fixed to the glass substrate, and the peeling electrification voltage was measured while peeling off the adhesive sheet of the specimen with a tensile tester at a peeling angle of about 180 degrees and a peeling speed of 40 m / min.

6. Whether stains occur after removing the adhesive sheet

After peeling off the pressure-sensitive adhesive sheet from the same specimen as that used in the measurement of the low-speed peeling force, it was observed whether or not the surface of the adhered object was contaminated by static electricity.

A: Unevenness on the surface of the adherend

B: When the surface of the adherend is stained

Manufacturing example 1. Preparation of acrylic copolymer (A)

80 parts by weight of 2-ethylhexyl acrylate (2-EHA) and 2 parts by weight of 4-hydroxybutyl acrylate (4-HBA) were added to a 1 L reactor equipped with a cooling device for nitrogen gas flow- , 8 parts by weight of 2-hydroxyethyl acrylate (2-HEA) and 10 parts by weight of polyethylene glycol monomethyl ether methacrylate (the number of moles of ethylene oxide unit: 9 moles), and 100 parts by weight of ethyl acetate as a solvent were added . Then, nitrogen gas was purged for 1 hour to remove oxygen, reacted for about 8 hours with addition of a reaction initiator (AIBN: azobisisobutyronitrile), and the reaction product was diluted with ethyl acetate to prepare an acrylic copolymer (A) . The viscosity of the copolymer (A) was about 2,500 cP and the solid content was about 45%.

Manufacturing example 2 to 10. Preparation of acrylic copolymers (B) to (J)

An acrylic copolymer was prepared in the same manner as in Production Example 1, except that the ratio of the monomers used in the preparation of the copolymer was changed as shown in Table 1 below.

Manufacturing example One 2 3 4 5 6 7 8 9 10 Copolymer A B C D E F G H I J EHA 80 69 70 75 80 71.5 71 50 60 78 BA 5 5 10 5 HBA 2 3 One 5 2 1.5 12 2 2 HEA 8 8 20 5 15 2 3 35 8 PEGMA 10 15 4 15 3 15 4 5 30 15 Solid content (%) 45 45 45 45 45 45 45 45 45 45 Viscosity (cP) 2500 2500 2900 2600 2450 2700 2500 4200 3000 2500 Content Unit: parts by weight
EHA: 2-ethylhexyl acrylate
BA: butyl acrylate
HBA: 4-hydroxybutyl acrylate
HEA: 2-hydroxyethyl acrylate
PEGMA: polyethylene glycol monomethyl ether methacrylate (number of moles of ethylene oxide added: 9 moles)

Example 1 to 6 and Comparative Example 1 to 4

Tinuvin-144, Tinuvin-765, Irganox 1010 or Irganox 2450 were blended in 100 parts by weight of each of the acrylic copolymers prepared in the above Preparation Example in the proportions shown in Table 2 below. After each combination was stored in a 45 ° C. dml oven for 28 days, the transparency, viscosity retention, and solids content of the copolymer were observed. The transparency of the copolymer was measured by visual observation of the copolymer after storage and when A was used as a transparent state and when haze was observed by a crystalline foreign matter or the like as B, .

Example Comparative Example One 2 3 4 5 6 One 2 3 4 Copolymer A A A C E F A A A F HA1 0.5 0.2 2.0 HA2 0.5 1.0 0.1 AO1 0.5 1.0 0.5 AO2 1.0 Content unit: 100 parts by weight of copolymer
HA1: Tinuvin-144 (manufactured by BASF)
HA2: Tinuvin-765 (manufactured by BASF)
AO1: Irganox 1010 (manufactured by BASF)
AO2: Irganox 2450 (manufactured by BASF)

Example Comparative Example One 2 3 4 5 6 One 2 3 4 transparency A A A A A A B B B B Maintain viscosity A A A A A A B A A A Maintain solid content A A A A A A A A A A Viscosity: A = initial viscosity change rate less than 15%, B = initial viscosity change rate more than 15%
Solids content: A = initial solid content less than 5%, B = solid content greater than 5%

Example 7

Preparation of pressure-sensitive adhesive composition

0.5 part by weight of Tinuvin-144 (manufactured by BASF) was added to 100 parts by weight of the acrylic polymer (A) of Production Example 1, and 100 parts by weight of the above polymer (A) was mixed with an isoboron diisocyanate crosslinking agent and hexamethylene di 5.0 parts by weight of a mixture of an isocyanate crosslinking agent (MHG-80B, manufactured by Asahi) and 0.5 part by weight of LiTFSi (lithium bis (trifluoromethanesulfonyl) imide) were uniformly blended and diluted to a proper concentration in consideration of coating properties to prepare a pressure-sensitive adhesive composition.

Production of pressure-sensitive adhesive sheet

The pressure-sensitive adhesive composition thus prepared was coated on one side of a PET (poly (ethylene terephthalate)) film (thickness: 38 占 퐉) and dried to form a uniform coating layer having a thickness of about 20 占 퐉. Subsequently, the adhesive layer was maintained at about 90 DEG C for about 3 minutes to induce a crosslinking reaction on the coating layer to produce a pressure-sensitive adhesive sheet.

Example 8 to 12 and Comparative Example 5 to 9

A pressure-sensitive adhesive composition was prepared in the same manner as in Example 7, except that the composition of the pressure-sensitive adhesive composition was changed as shown in Table 4, and the physical properties were also evaluated.

Example Comparative Example 7 8 9 10 11 12 5 6 7 8 9 Copolymer A B C D E F D G H I J Cross-linking agent 5.0 5.0 5.0 4.0 6.0 4.0 5.0 15.0 10.0 6.0 6.0 AS1 0.3 0.5 0.5 1.0 10.0 1.0 0.5 1.0 0.5 AS2 2.0 1.0 HA1 0.5 0.5 0.5 HA2 0.5 0.5 0.5 AO1 0.5 0.5 0.5 AO2 0.5 0.5 L 2.8 3.1 5.2 3.3 5.0 3.0 1.2 1.5 1.5 2.0 3.0 H 50 48 60 55 60 52 32 40 35 42 65 H / L 18 15 12 17 12 17 > 20 > 20 > 20 > 20 > 20 ESD 0.3 0.4 0.5 0.3 0.5 0.3 0.5 0.5 > 1.0 0.4 0.3 Stain occurrence A A A A A A B B A A A Component Ratio Unit: 100 parts by weight of copolymer
Crosslinking agent: MHG-80B, manufactured by Asahi
AS1: lithium bis (trifluoromethanesulfonyl) imide
AS2: N-methyl-N, N, N-tributylammonium bis (trifluoromethanesulfonyl) imide
HA1: Tinuvin-144 (manufactured by BASF)
HA2: Tinuvin-765 (manufactured by BASF)
AO1: Irganox 1010 (manufactured by BASF)
AO2: Irganox 2450 (manufactured by BASF)
L: Low-speed peel force (unit: gf / inch)
H: High-speed peel force (unit: gf / inch)
H / L: ratio of high-speed peeling force (H) to low-speed peeling force (L)
ESD: Peeling Voltage (Unit: kV)

Claims

A polymer comprising polymerized units derived from a monomer of formula 1; And a compound of formula (3): < EMI ID =
[Chemical Formula 1]

(3)

Q is hydrogen or an alkyl group, U is an alkylene group or an alkylidene group, Z is an alkyl group or an aryl group, m is a number of 1 to 20, and M ₁ to M ₅ are each independently an R ^{1 -N, (R 2) (} R 3) -C or ^{(R 4) (R 5)} -C , and, in said R ¹ is a hydrogen atom, alkyl group or alkoxy group, R ² and R ³ are each independently R ⁴ and R ⁵ are each independently a hydrogen atom or an alkyl group, L is an alkylene group or an alkylidene group, and P is an alkyl group or a substituent group of the following formula (4): wherein M ₂ to M ₄ at least one is a R ¹ -N, R ¹ -N of M _2, M ₃ or M ₄ M _1, immediately adjacent to the existing M _2, M _3, M ₄ or M ₅ is the (R ²⁾ ( R ³ ) -C):
[Chemical Formula 4]

In the 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, or alkoxy group, R ² and R ³ are an alkyl group independently, 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 the formula (4) is the 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).

The pressure-sensitive adhesive composition of claim 1, wherein the polymer further comprises a polymerized unit derived from a monomer of the formula:
(2)

In Formula 2, Q is hydrogen or an alkyl group, A and B are each independently an alkylene group or an alkylidene group, and n is a number of 0 to 10.

The pressure-sensitive adhesive composition according to claim 2, wherein the polymer comprises polymerized units derived from 1 to 20 parts by weight of the monomer of the formula (1) and 1 to 40 parts by weight of the monomer of the formula (2).

The pressure-sensitive adhesive composition according to claim 2, wherein the polymer comprises a polymerizable unit derived from a first monomer satisfying the following condition 1 and a second monomer represented by the following formula (2)
[Condition 1]
1 to 3 = a + bxn
[Condition 2]
4? A + b? N
B is the number of carbon atoms of the alkylene group or alkylidene group of B, and n is the number of carbon atoms of the alkylene group or alkylidene group defined in formula (2) Same as.

5. The pressure-sensitive adhesive composition according to claim 4, wherein the polymer comprises polymerized units derived from 1 to 30 parts by weight of the first monomer and 1 to 10 parts by weight of the second monomer.

2. The compound according to claim 1, wherein R ¹ in the general formula (3) is a hydrogen atom, an alkyl group having 1 to 8 carbon atoms or 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, Is, for example, an alkylene group having 4 to 12 carbon atoms or an alkylidene group having 2 to 10 carbon atoms.

The process according to claim 1, wherein the compound of formula (3) is bis (1,2,2,6,6-pentamethyl-4-piperidyl) sebacate, methyl 1,2,2,6,6- (1,1-dimethylethyl) -4-hydroxyphenyl] methyl] -2-butyl-1,3-bis (1,2, 3- dihydroxyphenyl) , 2,6,6-pentamethyl-4-piperidinyl) ester, bis (2,2,6,6-tetramethyl-4-piperidyl) sebacate or bis , 6,6-tetramethyl-4-piperidinyl) sebacate.

The pressure-sensitive adhesive composition according to claim 1, wherein the compound of Formula 3 is contained in an amount of 0.01 to 10 parts by weight based on 100 parts by weight of the polymer.

The pressure-sensitive adhesive composition according to claim 1, further comprising an aliphatic isocyanate crosslinking agent.

The pressure-sensitive adhesive composition according to claim 9, wherein the cross-linking agent comprises at least one selected from the group consisting of an aliphatic cyclic isocyanate compound and an aliphatic acyclic isocyanate compound.

11. The composition of claim 10, wherein the aliphatic cyclic isocyanate compound is isobornyl diisocyanate, methylenedicyclohexyl diisocyanate or cyclohexane diisocyanate; Dimers or trimers of the isocyanate compounds; Or a reaction product of the isocyanate compound and a polyol.

11. The composition of claim 10, 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 reaction product of the isocyanate compound and a polyol.

The pressure-sensitive adhesive composition according to claim 9, wherein the crosslinking agent is contained in an amount of 0.01 to 10 parts by weight based on 100 parts by weight of the polymer.

The pressure-sensitive adhesive composition according to claim 1, further comprising an ionic compound.

The method according to claim 1, wherein the adherend having a surface energy of 30 mN / m or less in a state in which the crosslinked structure is implemented has a peeling force measured at a peeling angle of 180 degrees and a peeling speed of 0.3 m / min from 1 gf / g / 25 mm.

The method according to claim 1, wherein the adherend having a surface energy of 30 mN / m or less in a state where the crosslinked structure is implemented has a peel force of 180 g / min and a peel rate of 30 m / 150 gf / 25 mm.

A surface protective base film; And a pressure-sensitive adhesive layer formed on one surface of the surface-protecting base film, wherein the pressure-sensitive adhesive layer comprises the pressure-sensitive adhesive composition according to any one of claims 1 to 16 crosslinked.

An optical element in which the protective film of claim 17 is attached to a surface.

The optical element according to claim 18, wherein the surface energy of the surface of the optical element is 30 mN / m or less and the pressure-sensitive adhesive layer of the protective film is attached to a surface of which surface energy is 30 mN / m or less.

A display device comprising the optical element of claim 18.