KR101914455B1 - Adhesive composition, adhesive and adhesive sheet - Google Patents

Abstract

A pressure-sensitive adhesive composition, a pressure-sensitive adhesive, and a pressure-sensitive adhesive sheet each having antistatic properties and excellent in all of stress relaxation and durability when applied to an optical member such as a polarizing plate.
The pressure-sensitive adhesive composition according to the present invention comprises a first (meth) acrylic acid ester polymer (A) having a weight average molecular weight of 500,000 to 3,000,000 and a second (meth) acrylic acid ester polymer (B) having a weight average molecular weight of 8,000 to 30,000, , The crosslinking agent (C) and the antistatic agent (D), and the ratio of the second (meth) acrylic acid ester polymer (B) to 100 parts by mass of the first (meth) acrylic acid ester polymer (A) (Meth) acrylic acid ester polymer (B) contains a monomer having a functional group (b1) which reacts with the crosslinking agent (C) as a constituent component, and the ratio of the monomer having the functional group (Meth) acrylic acid ester polymer (A) is more than 1% by mass and less than 50% by mass in the second (meth) acrylic acid ester polymer (B) (Meth) acrylic acid ester as a constituent component, It characterized in that it contains a monomer having a functional group (b1) than the cross-linking agent (C) with a low reactive functional groups (a1) of the polymer (B) as constituents.

Description

[0001] ADHESIVE COMPOSITION, ADHESIVE AND ADHESIVE SHEET [0002]

The present invention relates to a pressure-sensitive adhesive composition, a pressure-sensitive adhesive (a material obtained by crosslinking a pressure-sensitive adhesive composition), and a pressure-sensitive adhesive sheet, and more particularly to a pressure-sensitive adhesive composition, a pressure-sensitive adhesive and a pressure-sensitive adhesive sheet suitable for an optical member such as a polarizing plate.

Generally, in a liquid crystal panel, a pressure-sensitive adhesive layer formed of a pressure-sensitive adhesive composition is often used to adhere a polarizing plate or a retardation plate to a glass substrate of a liquid crystal cell or the like. However, since optical members such as a polarizing plate and a retarder are easily shrunk due to heat or the like, shrinkage occurs due to thermal history, and as a result, the pressure-sensitive adhesive layer laminated on the optical member can not follow shrinkage thereof, (So-called white peeling) due to the deviation of the optical axis of the optical member due to the stress at the time of shrinkage of the optical member.

As a method for preventing this, there are (1) a method of suppressing the shrinkage of the optical member by bonding a pressure-sensitive adhesive layer having a high adhesive force and an excellent shape stability to an optical member such as a polarizing plate, or (2) And a method of using a pressure-sensitive adhesive layer having a small stress at the time. As the method (1), it is effective to use a pressure-sensitive adhesive layer having a high storage elastic modulus as disclosed in Patent Document 1. [ On the other hand, in the method (2), it is effective to use a pressure-sensitive adhesive layer excellent in stress relaxation property capable of flexibly coping with deformation of the optical member. However, in the case of forming a pressure-sensitive adhesive layer excellent in stress relaxation property, conventionally, it has been necessary to design the crosslink density in the pressure-sensitive adhesive layer to be low. In this case, the strength of the pressure-sensitive adhesive layer itself is lowered and the durability is deteriorated.

Therefore, in Patent Documents 2 to 4, the pressure-sensitive adhesive property is imparted to the pressure-sensitive adhesive layer by appropriately softening the resulting pressure-sensitive adhesive composition by adding a plasticizer, a liquid paraffin, a urethane elastomer or the like to the acrylic pressure-sensitive adhesive instead of lowering the crosslinking density of the pressure- , Thereby trying to obtain a light leakage property and a durability.

However, the pressure-sensitive adhesive composition to which the plasticizer or liquid paraffin was added had a difficulty in breaching out the plasticizer or liquid paraffin over time as the pressure-sensitive adhesive layer to be formed over time. This has led to a fear of various problems such as lowered adhesion durability and contamination of the liquid crystal cell serving as an adherend. Further, in the pressure-sensitive adhesive composition to which the urethane elastomer is added, the upper limit of the amount of the urethane elastomer to be added is limited in order to maintain compatibility. Therefore, in the pressure-sensitive adhesive layer obtained from the pressure-sensitive adhesive composition, the improvement of the stress relaxation property tends to become insufficient. Furthermore, when the amount of the urethane elastomer to be added is increased in order to improve the stress relaxation property, the compatibility with the acrylic pressure-sensitive adhesive is lowered, and problems such as opacity have occurred. Thus, in the conventional art, it is difficult to fundamentally improve the light-leak resistance and durability of the pressure-sensitive adhesive layer formed of the pressure-sensitive adhesive composition for optical members.

However, the release sheet on which the pressure-sensitive adhesive layer is laminated, or the optical member such as the polarizing plate and the retardation plate is usually made of a plastic material. Therefore, the electrical insulation is high, and static electricity is liable to be generated when the release sheet is peeled off. When the polarizing plate and the retarder are attached to the liquid crystal cell in the state where the static electricity thus generated remains, scattering may occur in the alignment of the liquid crystal molecules. In addition, the presence of static electricity causes problems such as dust and waste .

Here, in order to obtain an effective antistatic property, it has been proposed to add an antistatic agent to the pressure-sensitive adhesive composition (for example, Patent Documents 5 to 8).

[Patent Document 1] JP-A-2006-235568 [Patent Document 2] JP-A-5-45517 [Patent Document 3] JP-A-9-137143 [Patent Document 4] JP-A-2005-194366 [Patent Document 5] JP-A-2005-194366 [Patent Document 6] JP-A 2007-316377 [Patent Document 7] JP-A-2008-95081 [Patent Document 8] JP-A-2009-155585

However, when an antistatic agent is added to the pressure-sensitive adhesive composition, there is a problem that the durability of the obtained pressure-sensitive adhesive is lower than usual. In this pressure sensitive adhesive, lowering the crosslinking density or adding a plasticizer or the like in order to impart stress relaxation property further reduces the durability as described above. Therefore, it becomes more difficult to impart stress relaxation property. Thus, even in the case of a pressure-sensitive adhesive having antistatic properties, both stress relaxation and durability in the relationship of contradiction were problems.

An object of the present invention is to provide a pressure-sensitive adhesive composition, a pressure-sensitive adhesive, and a pressure-sensitive adhesive sheet which are excellent in both stress relaxation and durability when they are applied to optical members such as polarizing plates having antistatic properties.

(Meth) acrylic acid ester polymer (A) having a weight average molecular weight of 500,000 to 3,000,000 and a second (meth) acrylic acid ester having a weight average molecular weight of 8,000 to 30,000 (B) relative to 100 parts by mass of the first (meth) acrylic acid ester polymer (A), wherein the second (meth) acrylic acid ester polymer (A) contains the polymer (B), the cross-linking agent (C), and the antistatic agent (B) comprises a monomer having a functional group (b1) capable of reacting with the crosslinking agent (C) as a constituent component, and the second (meth) acrylic acid ester polymer The proportion of the monomer having the functional group (b1) is more than 1% by mass and less than 50% by mass in the second (meth) acrylic acid ester polymer (B) ) Is a monomer having a functional group which reacts with the crosslinking agent (C) (A1) which is not contained in the second (meth) acrylic acid ester polymer (B) and is less reactive with the crosslinking agent (C) than the functional group (b1) (Invention 1).

The pressure-sensitive adhesive obtained by crosslinking the pressure-sensitive adhesive composition according to the invention (Invention 1) has antistatic properties and exhibits an appropriate cohesive force and excellent stress relaxation property. By using the pressure-sensitive adhesive having excellent stress relaxation property, a pressure-sensitive adhesive sheet excellent in both light leakage and durability can be obtained while exhibiting sufficient antistatic property when applied to an optical member such as a polarizing plate.

The first (meth) acrylic acid ester polymer (A) or the first (meth) acrylic acid ester polymer (A) and the second (meth) acrylic acid ester polymer (B) The monomer unit constituting the polymer preferably contains 5 to 50 mass% of an oxyalkylene group-containing monomer (Invention 2).

In the above inventions (inventions 1 and 2), the antistatic agent (D) is preferably an ionic compound (invention 3).

In the above invention (Invention 3), it is preferable that the ionic compound is at least one selected from the group consisting of a nitrogen-containing onium salt, a sulfur-containing onium salt, a phosphorus-containing onium salt, an alkali metal salt and an alkaline earth metal salt ).

In the invention (Invention 4), the alkali metal salt is preferably at least one selected from the group consisting of a lithium salt and a potassium salt (invention 5).

In the invention (inventions 1 to 5), the functional group (a1) in the first (meth) acrylic acid ester polymer (A) is a carboxyl group, and the functional group (b1) is a hydroxyl group, and the crosslinking agent (C) is an isocyanate crosslinking agent (invention 6).

In the above invention (inventions 1 to 5), the first (meth) acrylic acid ester polymer (A) preferably contains no carboxyl group-containing monomer as the monomer unit constituting the polymer or contains a carboxyl group-containing monomer (15% by mass or less) (invention 7).

In the invention (Invention 1 to 7), it is preferable that the second (meth) acrylic acid ester polymer (B) contains 3 to 40 mass% of a hydroxyl group-containing monomer as the functional group (b1).

In the above invention (Invention 6), the content of the isocyanate crosslinking agent is preferably from 0.1 to 3.5, based on the amount of the functional group (b1) in the second (meth) acrylic acid ester polymer (B) (Ninth aspect).

Secondly, the present invention provides a pressure-sensitive adhesive comprising the pressure-sensitive adhesive composition (Invention 1 to 9) cross-linked (Invention 10).

In the invention (Invention 10), the surface resistance value of the pressure-sensitive adhesive is preferably 3.0 x 10 ¹¹ ? / Sq or less (invention 11).

Thirdly, the present invention provides a pressure-sensitive adhesive sheet comprising a substrate and a pressure-sensitive adhesive layer, wherein the pressure-sensitive adhesive layer comprises the pressure-sensitive adhesive (Invention 10 and 11).

In the above invention (invention 12), it is preferable that the substrate is an optical member (invention 13).

Fourthly, the present invention relates to a pressure-sensitive adhesive sheet comprising two release sheets and a pressure-sensitive adhesive layer sandwiched between the release sheets so as to contact the release surfaces of the two release sheets, wherein the pressure- The present invention also provides a pressure-sensitive adhesive sheet comprising the pressure-sensitive adhesive sheet.

In the pressure-sensitive adhesive in which the pressure-sensitive adhesive composition according to the present invention is crosslinked, a three-dimensional network structure is formed by a chemical crosslinking structure in a low-molecular-weight polymer conventionally used as a plasticizer, and a plurality of high molecular weight By inserting the polymer, it is presumed that the high molecular weight polymers are constrained to each other and a pseudo crosslinked structure is formed between the high molecular weight polymers. As a result, the obtained pressure-sensitive adhesive exhibits antistatic properties and exhibits an appropriate cohesive force and excellent stress relaxation property. By using the pressure-sensitive adhesive having the excellent stress relaxation property, a pressure-sensitive adhesive sheet having both excellent leak resistance and durability can be obtained while exhibiting sufficient antistatic properties when applied to an optical member such as a polarizing plate.

1 is a cross-sectional view of a pressure-sensitive adhesive sheet according to a first embodiment of the present invention.
2 is a sectional view of a pressure-sensitive adhesive sheet according to a second embodiment of the present invention.
3 is a view showing a measurement area of a light leakage test in a polarizer with a pressure-sensitive adhesive layer.

Hereinafter, an embodiment of the present invention will be described.

[Adhesive composition]

The adhesive composition according to the present embodiment comprises a first (meth) acrylic acid ester polymer (A) having a weight average molecular weight (Mw) of 500,000 to 3,000,000 and a second (meth) acrylate polymer having a weight average molecular weight (Mw) (B), a cross-linking agent (C) and an antistatic agent (D), and preferably further contains a silane coupling agent (E). On the other hand, in the present specification, (meth) acrylic acid ester means both acrylic acid ester and methacrylic acid ester. Other similar terms are also the same. The term " polymer " also includes the concept of " copolymer ".

In the pressure-sensitive adhesive obtained by crosslinking the adhesive composition, the second (meth) acrylic acid ester polymer (B) (low molecular weight polymer) forms a three-dimensional network structure through the crosslinking agent (C) Two or more molecules of the (meth) acrylic acid ester polymer (A) (high molecular weight polymer) are inserted in the absence of direct chemical bonding or with very little chemical bonding, so that the polymers (A) It is presumed that it forms a constrained, pseudo-crosslinked structure (the structure thus estimated may hereinafter be referred to as " structure X "). The pressure-sensitive adhesive having the structure X has antistatic properties and exhibits an appropriate cohesive force and excellent stress relaxation property. Such a pressure-sensitive adhesive having excellent stress relaxation property is excellent in light-leak resistance when applied to an optical member such as a polarizing plate, and has excellent durability and can prevent lifting or peeling even under high-temperature conditions.

The (meth) acrylic acid ester polymer (A) or (B) may be obtained by copolymerizing a (meth) acrylic acid alkyl ester having 1 to 20 carbon atoms in the alkyl group, a monomer having an alkylene oxide moiety (oxyalkylene group-containing monomer) A copolymer of a monomer having a functional group (reactive functional group-containing monomer) that reacts with the monomer (C) and another monomer used by desirability is preferable. On the other hand, it is also preferable that the first (meth) acrylic acid ester polymer (A) does not contain the above-mentioned reactive functional group-containing monomer as a constitutional unit. It is also preferable that the second (meth) acrylic acid ester polymer (B) does not contain the above-mentioned oxyalkylene group-containing monomer as a constitutional unit.

Examples of the (meth) acrylic acid alkyl ester having 1 to 20 carbon atoms in the alkyl group include methyl (meth) acrylate, ethyl (meth) acrylate, propyl (meth) acrylate, n-butyl (meth) acrylate, n-pentyl (meth) acrylate, cyclohexyl (meth) acrylate, 2-ethylhexyl (meth) acrylate, isooctyl Silyl (meth) acrylate, palmityl (meth) acrylate, and stearyl (meth) acrylate. These may be used alone or in combination of two or more.

The first (meth) acrylic acid ester polymer (A) preferably contains 5 to 100 mass%, particularly preferably 30 to 90 mass% of a (meth) acrylic acid alkyl ester having 1 to 20 carbon atoms in the alkyl group By mass, more preferably from 40 to 80% by mass. When the content of the (meth) acrylic acid alkyl ester is in the range of 5 to 100 mass%, desired tackiness is obtained. Also, the content of the alkyl (meth) acrylate ester is within the range of 30 to 90 mass%, whereby the content of the oxyalkylene group-containing monomer and the reactive functional group-containing monomer in the polymer (A) can be secured.

The second (meth) acrylic acid ester polymer (B) preferably contains, as a constitutional unit, 5 to 99% by mass of a (meth) acrylic acid alkyl ester having 1 to 20 carbon atoms in the alkyl group, By mass, more preferably from 40 to 80% by mass. When the content of the (meth) acrylic acid alkyl ester is in the range of 5 to 99 mass%, desired tackiness can be obtained and the content of the reactive functional group-containing monomer in the polymer (B) can be ensured. Further, the content of the alkyl (meth) acrylate ester is within the range of 30 to 90 mass%, whereby the content of the oxyalkylene group-containing monomer in the polymer (B) can be secured.

Examples of the oxyalkylene group-containing monomer include 2-methoxyethyl (meth) acrylate, 2-ethoxyethyl (meth) acrylate, 2-methoxypropyl (meth) acrylate, 3-methoxypropyl (Meth) acrylate, 2-methoxybutyl (meth) acrylate, and 4-methoxybutyl (meth) acrylate. Further, a (meth) acrylic acid alkoxy ester having a polyalkylene glycol chain such as a polyethylene glycol chain of a terminal alkoxy group or a polypropylene glycol chain is also preferably used. Among them, 2-methoxyethyl (meth) acrylate is particularly preferable because it is excellent in compatibility with each monomer in the polymerization for obtaining the polymer (A) or (B). These may be used alone or in combination of two or more.

The oxyalkylene group-containing monomer is preferably a monomer containing only the first (meth) acrylic acid ester polymer (A) or the first (meth) acrylic acid ester polymer (A) and the second (meth) . When at least the first (meth) acrylic acid ester polymer (A) contains an oxyalkylene group-containing monomer as a constitutional unit, the antistatic property of the antistatic agent (D) is improved by the alkoxy moiety exhibiting hydrophilicity. Therefore, the content of the antistatic agent (D) in the adhesive composition according to the present embodiment can be reduced. On the other hand, when only the second (meth) acrylic acid ester polymer (B) has an oxyalkylene group-containing monomer as a constitutional unit, in the process of forming the three-dimensional network structure by the polymer (B) It is presumed that the polarity difference between the structural part and the polymer (A) is increased. Therefore, there is a fear that the optical characteristics are lowered by the phase separation of the two components, or the structure X is not sufficiently formed. Therefore, it is preferable to avoid this form.

The first (meth) acrylic acid ester polymer (A) preferably contains 5 to 50 mass%, particularly preferably 10 to 40 mass%, of the above-mentioned oxyalkylene group-containing monomer as a constituent unit, and more preferably 15 By mass to 35% by mass. The same applies when the second (meth) acrylic acid ester polymer (B) contains an oxyalkylene group-containing monomer as a constitutional unit. When the content of the oxyalkylene group-containing monomer is within the above range, the above-described excellent effect can be obtained and the content of the alkyl (meth) acrylate ester and the reactive functional group-containing monomer in the adhesive composition according to the present embodiment can be ensured .

On the other hand, examples of the reactive functional group-containing monomer include a monomer having a hydroxyl group in the molecule (a hydroxyl group-containing monomer), a monomer having a carboxyl group in the molecule (a carboxyl group-containing monomer), a monomer having an amino group in the molecule (an amino group-containing monomer) . On the other hand, examples of the monomer having a reactive functional group (a1) -containing monomer, the reactive functional group (b1) -containing monomer and the reactive functional group (b2) include the reactive functional group-containing monomer described herein. The selection of the kind is the same as described in the item of each monomer.

Examples of the hydroxyl group-containing monomer include 2-hydroxyethyl (meth) acrylate, 2-hydroxypropyl (meth) acrylate, 3-hydroxypropyl (meth) acrylate, 2-hydroxybutyl (Meth) acrylic acid hydroxyalkyl esters such as 3-hydroxybutyl (meth) acrylate and 4-hydroxybutyl (meth) acrylate. These may be used alone or in combination of two or more.

Examples of the carboxyl group-containing monomer include ethylenically unsaturated carboxylic acids such as acrylic acid, methacrylic acid, crotonic acid, maleic acid, itaconic acid and citraconic acid. These may be used alone or in combination of two or more.

Examples of the amino group-containing monomer include aminoethyl (meth) acrylate and n-butylaminoethyl (meth) acrylate. These may be used alone or in combination of two or more.

Examples of the other monomer include (meth) acrylic acid esters having an aliphatic ring such as cyclohexyl (meth) acrylate, (meth) acrylic acid esters having an aromatic ring such as phenyl (meth) acrylate, acrylamide, (Meth) acrylate having a non-cross-linkable tertiary amino group such as (meth) acrylic acid, N, N-dimethylaminoethyl (meth) acrylate, Acrylic ester, vinyl acetate, styrene, and the like. These may be used alone or in combination of two or more.

The second (meth) acrylic acid ester polymer (B) comprises a monomer (monomer containing a reactive functional group (b1)) having a functional group (b1) reacting with the crosslinking agent (C). The functional group contained in the polymer (B) and reacting with the crosslinking agent (C) is preferably substantially only the functional group (b1). On the other hand, " substantially the functional group (b1) only " allows the other functional group reacting with the crosslinking agent (C) to be contained to such an extent as not to interfere with the reactivity of the functional group (b1) and the crosslinking agent (C).

That is, the second (meth) acrylic acid ester polymer (B) comprises, as a constituent component, a monomer (monomer containing a reactive functional group (b2)) having a functional group (b2) having a lower reactivity with the crosslinking agent (C) than the functional group It is preferable that it is not contained. However, when the monomer containing the reactive functional group (b2) is contained as a constituent, it is preferable that the monomer contains an amount of 1/5 or less, particularly 1/10 or less, of the content of the monomer having a reactive functional group (b1) .

On the other hand, the reactive (meth) acrylic acid ester polymer (A) used in the second (meth) acrylic acid ester polymer (B) and the reactive monomers containing the reactive functional group (b1) The choice of the monomer containing the functional group (a1) is determined by the reactivity with the crosslinking agent (C) to be used. Details will be described later.

When the second (meth) acrylic acid ester polymer (B) contains the reactive functional group (b2) -containing monomer in an amount exceeding 1/5 of the content of the reactive functional group (b1) -containing monomer in the mass ratio, the durability There is a fear of lowering the temperature. When the number of reactive functional groups (b2) in the second (meth) acrylic acid ester polymer (B) is excessively large, a large amount of the reactive functional group (b2) remains in the three-dimensional network structure formed thereby, (Meth) acrylic acid ester polymer (A). As a result, the haze value may increase. It is also presumed that the three-dimensional network structure in which a large amount of the reactive functional group (b2) remains excessively restricts the mobility of the first (meth) acrylic acid ester polymer (A) inserted in the three-dimensional network structure. As a result, the stress relieving property of the obtained pressure sensitive adhesive is lowered, and the durability is sometimes deteriorated.

In addition, when the adhesive composition according to the present embodiment contains the silane coupling agent (E), the silane coupling agent (E) is a silane coupling agent having the reactive functional group (a1) of the first (meth) acrylic acid ester polymer Carboxyl group) and binds to the first (meth) acrylic acid ester polymer (A) having a high molecular weight. On the other hand, the binding referred to herein is not limited to the covalent bond but includes a hydrogen bond, a hydrophobic interaction, a van der Waals force, and the like. As a result, the alkoxysilyl group portion of the silane coupling agent (E) acts on the glass substrate, and thus it is presumed that the obtained pressure sensitive adhesive improves the adhesion with the glass substrate or the like to be adhered. If the second (meth) acrylic acid ester polymer (B) contains an excessive amount of the reactive functional group (b2) -containing monomer, the silane coupling agent (E) (meth) acrylic ester polymer (B) (particularly a carboxyl group) and binds to the second (meth) acrylic acid ester polymer (B) having a low molecular weight. As a result, the pressure-sensitive adhesive obtained is inferior in adhesion with the glass substrate or the like to which the pressure-sensitive adhesive is adhered, which may lower the durability of the pressure-sensitive adhesive layer.

The second (meth) acrylic acid ester polymer (B) contains 1% by mass or more of the monomer containing the reactive functional group (b1), and the upper limit thereof is less than 50% by mass. Preferably, the monomer containing the reactive functional group (b1) is contained in an amount of 5 to 40 mass%, particularly preferably 10 to 30 mass%, and more preferably 12 to 20 mass%. The degree of crosslinking of the second (meth) acrylic acid ester polymer (B) is preferred by containing the reactive functional group (b1) -containing monomer within the above range, and the degree of crosslinking of the second (meth) acrylic acid ester polymer (B) The stress relaxation property of the pressure-sensitive adhesive can be improved. As a result, a pressure-sensitive adhesive that combines durability and light-leak resistance can be obtained. When the content of the reactive functional group (b1) -containing monomer is 1% by mass or less, the crosslinking of the second (meth) acrylic acid ester polymer (B) is insufficient and the gel fraction is low, thereby lowering the durability . On the other hand, if the content of the reactive functional group (b1) -containing monomer is 50 mass% or more, the crosslinking of the second (meth) acrylic acid ester polymer (B) becomes excessive and the stress relaxation property may be deteriorated. On the other hand, when the upper limit of the content of the reactive functional group (b1) -containing monomer is 30 mass%, the obtained pressure-sensitive adhesive sheet has excellent resistance to light.

The polymerization forms of the second (meth) acrylic acid ester polymer (B) obtained by polymerizing a (meth) acrylic acid alkyl ester having 1 to 20 carbon atoms in the alkyl group and a monomer having a functional group reactive with the crosslinking agent (C) And may be a random copolymer or a block copolymer.

In the present embodiment, the second (meth) acrylic ester polymer (B) may be used singly or in combination of two or more kinds.

The weight average molecular weight of the second (meth) acrylic acid ester polymer (B) is 8,000 to 30,000, preferably 10,000 to 200,000, and particularly preferably 50,000 to 100,000. In other words, the second (meth) acrylic acid ester polymer (B) is a low molecular weight polymer component. In the present specification, the weight-average molecular weight is a polystyrene-reduced value measured by a gel permeation chromatography (GPC) method.

Since the weight average molecular weight of the second (meth) acrylic acid ester polymer (B) is within the above range, a three-dimensional network structure peculiar to the adhesive composition according to the present embodiment is formed, contributing to excellent stress relaxation property. That is, when the weight average molecular weight of the second (meth) acrylic acid ester polymer (B) is less than 8,000, a satisfactory three-dimensional network structure can not be obtained. On the other hand, when the weight average molecular weight of the second (meth) acrylic acid ester polymer (B) exceeds 30,000, the compatibility with the first (meth) acrylic acid ester polymer (A) decreases and the haze value of the pressure- , Etc., may be inferior in optical characteristics. Further, the insertion of the polymer (A) into the three-dimensional network structure formed by the polymer (B) becomes insufficient, and as a result, the resulting pressure-sensitive adhesive may be inferior in durability and reworkability.

The first (meth) acrylic acid ester polymer (A) preferably does not contain a monomer having a functional group which reacts with the crosslinking agent (C) as a constituent, or the functional group of the second (meth) acrylic acid ester polymer (a1) containing a functional group (a1) having a lower reactivity with the crosslinking agent (C) than the functional group (b1), and particularly preferably a crosslinking agent (C) ) As a constituent component.

The first (meth) acrylic acid ester polymer (A) may not contain a monomer having a functional group reactive with the crosslinking agent (C). However, it is preferable to contain the reactive functional group (a1) -containing monomer. In other words, when the polymer (A) contains the reactive functional group (a1), the reaction between the second (meth) acrylic acid ester polymer (B) and the crosslinking agent (C) may be promoted. Alternatively, when the silane coupling agent (E) is used, the reactive functional group (a1) of the first (meth) acrylic acid ester polymer (A) reacts with the silane coupling agent (E) The durability of adhesion to the glass surface can be made more suitable, which is preferable.

When the first (meth) acrylic acid ester polymer (A) contains the above-mentioned reactive functional group (a1) containing monomer, its content is usually 20 mass% or less, preferably 15 mass% or less, more preferably 10 mass% desirable. If the content of the reactive functional group (a1) -containing monomer exceeds 20 mass%, there is a fear that the glass transition temperature (Tg) of the first (meth) acrylic acid ester polymer (A) becomes excessively high and the stress relaxation property of the resulting pressure- have. On the other hand, from the viewpoint of imparting reworkability to the pressure-sensitive adhesive, the content of the reactive functional group (a1) -containing monomer is preferably 15 mass% or less.

In comparison with the monomer containing the reactive functional group (b1) contained in the second (meth) acrylic acid ester polymer (B), the content of the reactive functional group (a1) -containing monomer contained in the first (meth) acrylic acid ester polymer (A) The ratio of the second (meth) acrylic acid ester polymer (A) in the first (meth) acrylic acid ester polymer (A) to the second (meth) acrylic acid ester polymer (B) of the reactive functional group ) Is preferable. As a result, the reaction between the reactive functional group (a1) and the crosslinking agent (C) contained in the first (meth) acrylic acid ester polymer (A) (b1) and the crosslinking agent (C) can be surely reacted. As a result, the stress relaxation property of the resulting pressure-sensitive adhesive can be improved.

The first (meth) acrylic acid ester polymer (A) does not contain a monomer having a functional group having a reactivity with the crosslinking agent (C) equal to or higher than that of the reactive functional group (b1) of the second (meth) acrylic acid ester polymer . However, if contained, the content of the monomer having the functional group in the molecule is preferably 1% by mass or less, more preferably 0.5% by mass or less, in the polymer (A). If the content of the monomer is more than 1% by mass, there is a fear that the reaction of the second (meth) acrylic acid ester polymer (B) to be reacted with the crosslinking agent (C) may be inhibited. As a result, the desired stress relaxation property may not be obtained.

Here, the polymerization forms of the first (meth) acrylic acid ester polymer (A) obtained by polymerizing the (meth) acrylic acid alkyl ester having 1 to 20 carbon atoms in the alkyl group and the reactive functional group-containing monomer may be a random copolymer, It may be a copolymer.

In the present embodiment, the first (meth) acrylic acid ester polymer (A) may be used singly or in combination of two or more kinds.

The weight average molecular weight of the first (meth) acrylic acid ester polymer (A) is from 500,000 to 3,000,000, preferably from 700,000 to 250,000, and particularly preferably from 1 million to 2,000,000. In other words, the first (meth) acrylic acid ester polymer (A) is a high molecular weight polymer component.

It is presumed that the structure (X) is formed satisfactorily because the weight average molecular weight of the first (meth) acrylic acid ester polymer (A) is within the above range and the polymer (A) has a relatively large molecular weight.

Here, if the weight average molecular weight of the first (meth) acrylic acid ester polymer (A) is less than 500,000, the obtained pressure sensitive adhesive gel fraction may be low, and durability and reworkability may be poor. When the weight average molecular weight of the first (meth) acrylic acid ester polymer (A) exceeds 3,000,000, compatibility with the second (meth) acrylic acid ester polymer (B) is deteriorated and the stress relaxation property of the resultant pressure sensitive adhesive There is a concern.

The ratio of the second (meth) acrylic acid ester polymer (B) to 100 parts by mass of the first (meth) acrylic acid ester polymer (A) is 5 to 50 parts by mass, preferably 5 to 40 parts by mass, Particularly preferred is the part by mass.

The pressure sensitive adhesive obtained from the adhesive composition containing the first (meth) acrylic acid ester polymer (A) and the second (meth) acrylic acid ester polymer (B) in the above ratio is presumed to form the structure X well.

Examples of the crosslinking agent (C) include an isocyanate crosslinking agent, an epoxy crosslinking agent, an aziridine crosslinking agent, and a metal chelating crosslinking agent.

The isocyanate-based crosslinking agent includes at least a polyisocyanate compound. Examples of the polyisocyanate compound include aromatic polyisocyanates such as tolylene diisocyanate, diphenylmethane diisocyanate and xylylene diisocyanate, aliphatic polyisocyanates such as hexamethylene diisocyanate, isophorone diisocyanate, hydrogenated diphenylmethane di An alicyclic polyisocyanate such as isocyanate and the like and a reaction product thereof with a low molecular active hydrogen-containing compound such as a burette, isocyanurate, and further ethylene glycol, propylene glycol, neopentyl glycol, trimethylol propane, And duct bodies. Among them, a tolylene diisocyanate (TDI) adduct of trimethylolpropane is particularly preferable because it can impart appropriate rigidity and flexibility to the resulting crosslinked structure.

Examples of the epoxy crosslinking agent include 1,3-bis (N, N'-diglycidylaminomethyl) cyclohexane, N, N, N ', N'-tetraglycidyl-m- , Ethylene glycol diglycidyl ether, 1,6-hexanediol diglycidyl ether, trimethylol propane diglycidyl ether, diglycidyl aniline, and diglycidyl amine.

Examples of the aziridine crosslinking agent include diphenylmethane-4,4'-bis (1-aziridinecarboxamide), trimethylolpropane tri- beta -aziridinylpropionate, tetramethylol methanetri- aziridinyl propionate, toluene-2,4-bis (1-aziridinecarboxamide), triethylene melamine, bisisopthaloyl-1- (2-methyl aziridine), tris- -Methyl aziridine) phosphine, trimethylolpropane tri- beta - (2-methyl aziridine) propionate, and the like.

As the metal chelate-based crosslinking agent, chelate compounds such as aluminum, zirconium, titanium, zinc, iron and tin can be used as the metal atom, but aluminum chelate compounds are preferable from the viewpoint of performance. Examples of the aluminum chelate compound include diisopropoxy aluminum monooleate acetoacetate, monoisopropoxy aluminum bisoleyl acetoacetate, monoisopropoxy aluminum monooleate monoethylacetoacetate, diisopropoxy aluminum Mono lauryl acetoacetate, diisopropoxyaluminum monostearyl acetoacetate, diisopropoxyaluminum monoisostearyl acetoacetate, and the like.

The content of the crosslinking agent (C) is preferably such that the crosslinking group (for example, an isocyanate group) of the crosslinking agent (C) is the reactive functional group (b1) of the second (meth) acrylic acid ester polymer (B) The amount is usually 0.05 to 5 equivalents, preferably 0.1 to 3.5 equivalents, and particularly preferably 0.3 to 1.0 equivalents. When the amount of the crosslinkable group is less than 0.05 equivalents, the gel fraction of the obtained pressure sensitive adhesive is low, and there is a possibility that sufficient cohesive force can not be exerted. When the amount of the crosslinkable group is 0.1 equivalents or more, particularly 0.3 equivalents or more, the resulting pressure-sensitive adhesive can be more excellent in durability. On the other hand, when the amount of the crosslinkable group is 3.5 equivalents or less, the pressure-sensitive adhesive obtained can be excellent in reworkability. In addition, when the amount of the crosslinkable group is 1.0 equivalent or less, it is presumed that the crosslinking agent (C) contributes only to the formation of the three-dimensional network structure of the polymer (B), thereby effectively preventing crosslinking of the polymer (A). As a result, the obtained pressure sensitive adhesive exhibits excellent stress relaxation property.

In the present embodiment, the reactive functional group (b1) of the second (meth) acrylic acid ester polymer (B) and the reactive functional group (a1) of the first (meth) acrylic acid ester polymer A plurality of kinds of objects may be used in combination if the kind of the cross-linking agent is the same as the relationship of reactivity with all. From the viewpoint of facilitating control of the three-dimensional network structure formed by the second (meth) acrylic acid ester polymer (B), it is preferable to use only one kind of crosslinking agent as the functional group, for example, only an isocyanate crosslinking agent is used Further, it is particularly preferable to use only one crosslinking agent as a compound.

As the combination of the cross-linking agent (C) and the reactive functional group-containing monomer of each of the (meth) acrylic acid ester polymer (A) and the (meth) acrylic acid ester polymer (B), in the case of the isocyanate- Examples of the monomer containing a functional group (a1) include a carboxyl group-containing monomer, a reactive functional group (b1) -containing monomer (b1) containing a hydroxyl group-containing monomer or an amino group-containing monomer (particularly a hydroxyl group- A carboxyl group-containing monomer is preferably selected.

On the other hand, when the crosslinking agent (C) is an epoxy crosslinking agent, an aziridine crosslinking agent or a metal chelating crosslinking agent, the reactive functional group (b1) of the hydroxyl group-containing monomer, the polymer (B) As the monomer containing a carboxyl group and the monomer containing a reactive functional group (b2) of the polymer (B), a hydroxyl group-containing monomer is preferably selected.

The flexibility of the bond formed between the crosslinking agent (C) and the polymer (B) and the mildness of the crosslinking reaction, and furthermore, the reactive group of the polymer (A) reacts appropriately with the silane coupling agent (E) to improve the adhesion durability of the resulting pressure- , The crosslinking agent (C) is preferably an isocyanate crosslinking agent, a monomer containing a reactive functional group (a1) of the polymer (A) and a monomer containing a reactive functional group (b1) of the polymer (B) , And that the monomer containing a reactive functional group (b2) is not used.

The antistatic agent (D) is not particularly limited as long as the antistatic agent (D) can impart antistatic properties to the resulting pressure-sensitive adhesive without impairing the effects of the present invention. Examples thereof include ionic compounds and surfactants. Among them, Compounds are preferred. The ionic compound may be a liquid or a solid. Herein, the ionic compound in the present specification means a compound in which positive ions and negative ions are mainly bonded together by an electrostatic attracting force.

As the ionic compound, a nitrogen-containing onium salt, a sulfur-containing onium salt, a zinc onium salt, an alkali metal salt and an alkaline earth metal salt are preferable. On the other hand, as the alkali metal salt, a lithium salt and a potassium salt are preferable. Specific examples of such an antistatic agent (D) include N-butyl-4-methylpyridinium hexafluorophosphite, N-hexyl-4-methylpyridinium hexafluorophosphite, N-butyl- , Bis (fluorosulfonylimide) potassium (KFSI), bis (trifluoromethanesulfonylimide) potassium (KTFSI), bis (fluorosulfonylimide) lithium (LiFSi), bis (trifluoromethanesulfonyl) (LiTFSI), N-butyl-2-hexylpyridinium bis (trifluoromethanesulfonyl) imide, and the like. The above antistatic agent (D) may be used singly or in combination of two or more kinds.

The content of the antistatic agent (D) in the adhesive composition according to the present embodiment is preferably from 0.1 to 30 mass%, more preferably from 0.5 to 20 mass%, further preferably from 1.0 to 10.0 mass% . When the content of the antistatic agent (D) is within the above range, the antistatic property can be effectively exhibited and the content of the other components (A) to (C) in the adhesive composition according to the present embodiment can be ensured.

On the other hand, the antistatic agent (D) is preferably used alone, but it is also preferable to use a dispersant in combination. When the solubility of the antistatic agent (D) in the adhesive composition is insufficient, solubility can be improved by using a dispersant in combination.

As the dispersing agent, for example, alkylene glycol dialkyl ether and the like are preferably used. Specific examples of the alkylene glycol dialkyl ether include octaethylene glycol dibutyl ether, octaethylene glycol diethyl ether, octaethylene glycol dimethyl ether, hexaethylene glycol dibutyl ether, hexaethylene glycol diethyl ether, hexaethylene glycol dimethyl ether, Tetraethylene glycol diethyl ether, tetraethylene glycol dimethyl ether (hereinafter sometimes referred to as " tetraglyl "), triethylene glycol diethyl ether, triethylene glycol dimethyl ether, etc. have. These dispersants may be used singly or in combination of two or more kinds.

The blending amount of the dispersant is preferably 0.5 to 1.5, more preferably 0.7 to 1.2, and particularly preferably 0.9 to 1.1 in the molar ratio to the antistatic agent (D).

On the other hand, when the first (meth) acrylic acid ester polymer (A) or the first (meth) acrylic acid ester polymer (A) and the second (meth) acrylic acid ester polymer (B) When it is contained as a constitutional unit, the content of the antistatic agent (D) can be reduced. Concretely, the content in the adhesive composition according to the present embodiment may be in the range of preferably 0.1 to 10.0% by mass, particularly preferably 0.5 to 5.0% by mass, and more preferably 1.0 to 3.0% by mass .

The adhesive composition according to the present embodiment preferably further contains a silane coupling agent (E). When the first (meth) acrylic acid ester polymer (A) has a carboxyl group, the organic reactive group or the like of the silane coupling agent (E) and the first (meth) acrylic acid ester polymer ) On the other side, and the alkoxysilyl group of the silane coupling agent (E) on the other side acts on the surface of the adherend such as a glass substrate. For this reason, for example, when the polarizing plate is bonded to a liquid crystal glass cell or the like, adhesion between the pressure-sensitive adhesive and the liquid crystal glass cell becomes better. On the other hand, when the reactive functional group (a1) of the polymer (A) is other than a carboxyl group, a silane coupling agent (E) having an organic reactive group acting on the reactive functional group (a1) is appropriately selected.

The silane coupling agent (E) is preferably an organosilicon compound having at least one alkoxysilyl group in the molecule and having good compatibility with the pressure-sensitive adhesive component and having optical transparency, for example, substantially transparent. The amount of the silane coupling agent (E) to be added is preferably 0.01 to 1.0 part by mass, more preferably 0.05 to 0.5 part by mass with respect to 100 parts by mass of the first (meth) acrylic acid ester polymer (A).

Specific examples of the silane coupling agent (E) include polymerizable unsaturated group-containing silicon compounds such as vinyltrimethoxysilane, vinyltriethoxysilane and methacryloxypropyltrimethoxysilane, 3-glycidoxypropyltrimethoxysilane , Silicon compounds having an epoxy structure such as 2- (3,4-epoxycyclohexyl) ethyltrimethoxysilane, 3-aminopropyltrimethoxysilane, N- (2-aminoethyl) Silane, amino group-containing silicon compounds such as N- (2-aminoethyl) -3-aminopropylmethyldimethoxysilane, 3-chloropropyltrimethoxysilane, 3-isocyanatepropyltriethoxysilane and the like. These may be used singly or in combination of two or more kinds.

Various additives generally used in acrylic pressure sensitive adhesives such as a tackifier, an antioxidant, an ultraviolet absorber, a light stabilizer, a softening agent, a filler, a refractive index adjuster and the like may be added to the adhesive composition, if desired.

[Process for producing adhesive composition]

The adhesive composition is prepared by preparing each of the first (meth) acrylic acid ester polymer (A) and the second (meth) acrylic acid ester polymer (B) and mixing them, and at the same time, An antistatic agent (D) and, if desired, a silane coupling agent (E).

As specific preferred examples, the (meth) acrylic acid ester polymers (A) and (B) are separately prepared by a usual radical polymerization method. The polymerization of the (meth) acrylic acid ester polymers (A) and (B) can be carried out by a solution polymerization method or the like using a polymerization initiator if desired. Examples of the polymerization solvent include ethyl acetate, n-butyl acetate, isobutyl acetate, toluene, acetone, hexane, methyl ethyl ketone, and the like.

Examples of the polymerization initiator include an azo compound, an organic peroxide, and the like, and two or more types may be used in combination. Examples of the azo compound include azo compounds such as 2,2'-azobisisobutyronitrile, 2,2'-azobis (2-methylbutyronitrile), 1,1'-azobis (cyclohexane 1-carbo Nitrile, 2,2'-azobis (2,4-dimethylvaleronitrile), 2,2'-azobis (2,4-dimethyl-4-methoxy valeronitrile), dimethyl 2,2'-azo Azo compounds such as bis (2-methylpropionate), 4,4'-azobis (4-cyanovaleric acid), 2,2'-azobis (2-hydroxymethylpropionitrile) Bis [2- (2-imidazolin-2-yl) propane] and the like.

Examples of the organic peroxide include benzoyl peroxide, t-butyl perbenzoate, cumene hydroperoxide, diisopropyl peroxydicarbonate, di-n-propyl peroxydicarbonate, di (2-ethoxyethyl) peroxydicarbonate , t-butyl peroxyneodecanoate, t-butyl peroxybibarate, (3,5,5- (trimethylhexanoyl) peroxide, dipropionyl peroxide, and diacetyl peroxide.

On the other hand, in the above-mentioned polymerization step, the weight average molecular weight of the resulting polymer can be controlled by blending a chain transfer agent such as 2-mercaptoethanol.

Next, the solutions of the obtained polymers (A) and (B) are mixed and a diluting solvent is added. Thereafter, a crosslinking agent (C), an antistatic agent (D) and, if desired, a silane coupling agent (E) are added and thoroughly mixed to obtain a sticky composition (coating solution) diluted with a solvent.

Examples of the diluting solvent for diluting the adhesive composition into a coating solution include aliphatic hydrocarbons such as hexane, heptane and cyclohexane, aromatic hydrocarbons such as toluene and xylene, halogenated hydrocarbons such as methylene chloride and ethylene chloride, , Alcohols such as propanol, butanol and 1-methoxy-2-propanol, ketones such as acetone, methyl ethyl ketone, 2-pentanone, isophorone and cyclohexanone, esters such as ethyl acetate and butyl acetate, A cellosolve solvent such as Solv may be used.

The concentration and viscosity of the coating solution thus produced are not particularly limited and may be suitably selected in accordance with the circumstances as long as they are in a coating-capable range. For example, it is diluted so that the concentration of the adhesive composition is 10 to 40% by mass. On the other hand, when a coating solution is obtained, addition of a diluting solvent or the like is not a necessary condition, and it is not necessary to add a diluting solvent if the viscosity is such that the adhesive composition can be coated. In this case, the adhesive composition becomes a coating solution as it is.

〔adhesive〕

The pressure-sensitive adhesive according to the present embodiment is obtained by crosslinking the pressure-sensitive adhesive composition. The crosslinking of the adhesive composition can be carried out by heat treatment. On the other hand, the heat treatment may also serve as a drying treatment for volatilizing a diluting solvent or the like of the adhesive composition.

In the case of performing the heat treatment, the heating temperature is preferably 50 to 150 占 폚, particularly preferably 70 to 120 占 폚. The heating time is preferably 30 seconds to 3 minutes, and more preferably 50 seconds to 2 minutes. Furthermore, it is particularly preferable to set a curing period of about 1 to 2 weeks at room temperature (for example, 23 DEG C, 50% RH) after the heat treatment.

The second (meth) acrylic acid ester polymer (B) is crosslinked by the crosslinking agent (C) by the above heat treatment (and curing), and the first (meth) acrylic acid ester polymer (A) It is assumed that the structure X is formed. When the first (meth) acrylic acid ester polymer (A) has a carboxyl group, the first (meth) acrylic acid ester polymer (A) reacts with the silane coupling agent (E) to form a glass substrate It is possible to improve the durability of adhesion.

The surface resistivity of the pressure-sensitive adhesive according to the present embodiment is preferably 3.0 x 10 ¹¹ ? / Sq or less, more preferably 1.0 x 10 ¹¹ ? / Sq or less, and further preferably 8.0 x 10 ¹⁰ ? / Sq or less. When the surface resistance value is less than the above value, sufficient antistatic property can be exhibited. In this embodiment, even when the content of the antistatic agent (D) in the adhesive composition is 3% by mass or less, sufficient antistatic properties can be exhibited as described above.

The adhesive force of the pressure-sensitive adhesive according to the present embodiment is preferably 0.1 to 50 N / 25 mm, more preferably 0.5 to 30 N / 25 mm, and further preferably 3.0 to 20 N / 25 mm . On the other hand, the adhesive force referred to herein means a 180 ° pulling off adhesive force (peeling speed 300 mm / min) in accordance with JIS Z0237. The adhesive force is applied to an adherend, pressurized at 0.5 MPa at 50 캜 for 20 minutes, % RH for 24 hours. When the adhesive force is within the above range, it is possible to prevent lifting or peeling, etc., when applied to an optical member such as a polarizing plate.

In addition, the pressure sensitive adhesive according to the present embodiment preferably has a gel fraction of 30 to 90%, particularly preferably 40 to 80%, further preferably 45 to 75%. When the degree of crosslinking of the pressure-sensitive adhesive according to the present embodiment is in the above range, the three-dimensional network structure formed by the crosslinking of the second (meth) acrylic acid (meth) acrylic acid is satisfactorily formed, All of the durability can be excellent.

On the other hand, the adhesive gel fraction is a value at the time of pasting (past the curing period). Specifically, it means a gel fraction after the adhesive composition is applied to a release sheet, heat-treated, and then stored at 23 ° C and 50% RH for 7 days. This is because the value of the adhesive gel fraction fluctuates before the curing period elapses. From this point of view, when it is unclear whether the curing period has elapsed, it is preferable that the gel fraction is maintained within the above range after being stored for 7 days under the environment of 23 ° C and 50% RH.

The pressure-sensitive adhesive described above can be preferably used for an optical member. For example, the pressure-sensitive adhesive described above can be used preferably for optical members such as adhesion between optical members such as a polarizing plate (polarizing film) and a retardation film (retardation film), a polarizing plate Film) and a glass substrate. The pressure-sensitive adhesive according to the present embodiment has antistatic properties, so that static electricity is not generated, and defects due to static electricity can be effectively suppressed. Further, since the pressure-sensitive adhesive layer formed by the pressure-sensitive adhesive has excellent stress relaxation properties, even if the dimensional change of the adherend is great, the stress that can be generated by the dimensional change can be absorbed and alleviated by the pressure- Therefore, it is not peeled off from the adherend for a long term, and light leakage can be effectively prevented when the optical member is used as described above. In other words, the pressure-sensitive adhesive according to the present embodiment has both antireflection properties and durability while having antistatic properties.

[Adhesive sheet]

1, the pressure-sensitive adhesive sheet 1A according to the first embodiment comprises a release sheet 12, a pressure-sensitive adhesive layer 11 laminated on the release surface of the release sheet 12, And a substrate 13 laminated on the pressure-sensitive adhesive layer 11. [

2, the pressure-sensitive adhesive sheet 1B according to the second embodiment is provided so as to contact two release sheets 12a and 12b and the release faces of the two release sheets 12a and 12b And a pressure-sensitive adhesive layer 11 sandwiched between the two release sheets 12a and 12b. On the other hand, the release surface of the release sheet in the present specification means a surface having release properties in the release sheet, and includes both the surface subjected to the release treatment and the surface exhibiting the release property without performing the release treatment.

In any of the pressure-sensitive adhesive sheets 1A, 1B, the pressure-sensitive adhesive layer 11 is a pressure-sensitive adhesive obtained by crosslinking the above-mentioned pressure-sensitive adhesive composition.

The thickness of the pressure-sensitive adhesive layer 11 is appropriately determined depending on the purpose of use of the pressure-sensitive adhesive sheets 1A and 1B, but is usually in the range of 5 to 100 m, preferably 10 to 60 m. For example, When it is used as a pressure-sensitive adhesive layer, it is preferably 10 to 50 m, especially 10 to 30 m.

The base material (13) is not particularly limited, and any material used as a base sheet of a conventional adhesive sheet can be used. For example, woven or nonwoven fabric using fibers of rayon, acrylic, polyester or the like other than the desired optical member; Papers such as coated paper, glossy paper, impregnated paper, and coated paper; Metal foil such as aluminum and copper; Foams such as urethane foams and polyethylene foams; A polyethylene film, a polyethylene film, a polypropylene film, a cellulose film such as triacetylcellulose, a polyvinyl chloride film, a polyvinylidene chloride film, a polyvinylidene chloride film, a polyvinylidene chloride film, a polyethylene terephthalate film, A plastic film such as a vinyl alcohol film, an ethylene-vinyl acetate copolymer film, a polystyrene film, a polycarbonate film, an acrylic resin film, a norbornene resin film, and a cycloolefin resin film; And a laminate of two or more kinds. The plastic film may be one-axis extended or two-axis extended.

Examples of the optical member include a polarizing plate (polarizing film), a polarizer, a retardation film (phase difference film), a viewing angle compensating film, a luminance improving film, a contrast enhancing film and a liquid crystal polymer film. Among them, the polarizing plate (polarizing film) is easy to shrink and has a large dimensional change, so that it is suitable as an object for forming the pressure-sensitive adhesive (the pressure-sensitive adhesive layer 11) of the present embodiment from the viewpoint of resistance to light leakage.

The thickness of the base material 13 varies depending on the type thereof. For example, in the case of an optical member, it is usually 10 m to 500 m, preferably 50 m to 300 m.

Examples of the release sheets 12, 12a and 12b include a polyethylene film, a polypropylene film, a polybutene film, a polybutadiene film, a polymethylpentene film, a polyvinyl chloride film, a vinyl chloride copolymer film, a polyethylene terephthalate film (Meth) acrylate copolymer film, an ethylene / (meth) acrylic acid ester copolymer film, a polystyrene film, a polyethylene naphthalate film, a polybutylene terephthalate film, a polyurethane film, an ethylene vinyl acetate film, an ionomer resin film, , A polycarbonate film, a polyimide film, a fluororesin film, or the like can be used. Such a crosslinked film may also be used. Furthermore, such a laminated film may be used.

The peeling surface of the release sheet (particularly, the surface in contact with the pressure-sensitive adhesive layer 11) is preferably peeled. Examples of the releasing agent used in the peeling treatment include an alkyd type, a silicone type, a fluorine type, an unsaturated polyester type, a polyolefin type, and a wax type releasing agent.

The thickness of the release sheets 12, 12a, 12b is not particularly limited, but is usually about 20 to 150 mu m.

In order to produce the pressure-sensitive adhesive sheet 1A, a solution (coating solution) containing the pressure-sensitive adhesive composition is coated on the release surface of the release sheet 12, heat treatment is performed to form the pressure-sensitive adhesive layer 11, And the base material 13 is laminated on the pressure-sensitive adhesive layer 11. Then, it is preferable to set the curing period.

The conditions of the heat treatment and curing are as described above.

In order to produce the pressure-sensitive adhesive sheet 1B, a coating solution containing the pressure-sensitive adhesive composition is applied to the release surface of one release sheet 12a (or 12b) and heat treatment is performed to form a pressure- , The peeling surface of the other release sheet 12b (or 12a) is superimposed on the pressure-sensitive adhesive layer 11.

As a method of applying the coating solution, for example, a bar coating method, a knife coating method, a roll coating method, a braiding coating method, a die coating method, a gravure coating method and the like can be used.

For example, a polarizing plate is used as the base material 13 of the pressure-sensitive adhesive sheet 1A, and a release sheet 12 of the pressure-sensitive adhesive sheet 1A is used for manufacturing a liquid crystal display device composed of a liquid crystal cell and a polarizing plate, And the exposed pressure-sensitive adhesive layer 11 and the liquid crystal cell are laminated together.

For example, to manufacture a liquid crystal display device in which a retarder plate is disposed between a liquid crystal cell and a polarizing plate, one of the release sheets 12a (or 12b) of the pressure-sensitive adhesive sheet 1B is peeled , And the exposed pressure-sensitive adhesive layer 11 of the pressure-sensitive adhesive sheet 1B and the retarder are bonded. Next, the release sheet 12 of the pressure-sensitive adhesive sheet 1A using the polarizing plate as the base material 13 is peeled off, and the exposed pressure-sensitive adhesive layer 11 of the pressure-sensitive adhesive sheet 1A is bonded to the retarder. Further, the other release sheet 12b (or 12a) is peeled from the pressure-sensitive adhesive layer 11 of the pressure-sensitive adhesive sheet B, and the exposed pressure-sensitive adhesive layer 11 of the pressure-sensitive adhesive sheet B is bonded to the liquid- .

According to the above-mentioned pressure-sensitive adhesive sheets 1A, 1B, since the pressure-sensitive adhesive layer 11 has antistatic properties, no static electricity is generated and the defects caused by the static electricity can be effectively suppressed. Further, since the pressure-sensitive adhesive layer 11 has excellent stress relaxation properties, even if it is applied, for example, to adhesion of a polarizing plate, the pressure that can be generated by the deformation of the polarizing plate can be absorbed and alleviated by the pressure- Whereby it is estimated that an excellent resistance to light leakage and a high durability are exhibited.

The embodiments described above are described for the purpose of facilitating understanding of the present invention and are not described for limiting the present invention. Therefore, each element disclosed in the above embodiment is intended to include all design modifications and equivalents falling within the technical scope of the present invention.

For example, the release sheet 12 of the pressure-sensitive adhesive sheet 1A may be omitted, and either one of the release sheets 12a and 12b in the pressure-sensitive adhesive sheet 1B may be omitted.

[Examples]

Hereinafter, the present invention will be described in more detail with reference to Examples and the like, but the scope of the present invention is not limited to these Examples and the like.

[Example 1]

 1. Preparation of Polymer (A)

75.0 parts by mass of n-butyl acrylate, 20.0 parts by mass of 2-methoxyethyl acrylate, 5.0 parts by mass of acrylic acid, 200 parts by mass of ethyl acetate, and 2 parts by mass of 2-ethylhexyl acrylate were charged in a reaction vessel equipped with a stirrer, a thermometer, a reflux condenser, , And 0.08 parts by mass of 2 " -azobisisobutyronitrile were placed, and the air in the reaction vessel was replaced with nitrogen gas. While stirring in this nitrogen atmosphere, the reaction solution was heated to 60 占 폚, allowed to react for 16 hours, and then cooled to room temperature. Here, a part of the obtained solution was measured for molecular weight by the method described below, and the formation of the polymer (A) having a weight average molecular weight of 1,200,000 was confirmed.

2. Preparation of Polymer (B)

85.0 parts by mass of n-butyl acrylate, 15.0 parts by mass of 2-hydroxyethyl acrylate, 200 parts by mass of ethyl acetate, 2, 2 " -azo 0.16 parts by mass of bisisobutylonitrile and 0.3 parts by mass of 2-mercaptoethanol were placed, and the air in the reaction vessel was replaced with nitrogen gas. While stirring in this nitrogen atmosphere, the reaction solution was heated to 70 占 폚, allowed to react for 6 hours, and then cooled to room temperature. Here, a part of the obtained solution was subjected to measurement of the molecular weight by the method described later, and production of the polymer (B) having a weight average molecular weight of 60,000 was confirmed.

3. Preparation of adhesive composition

After mixing 100 parts by mass (solid content conversion value) of the polymer (A) obtained in the above step (1) and 15 parts by mass (solid content conversion value) of the polymer (B) obtained in the above step (2) , 2.21 parts by mass of a tolylene diisocyanate (TDI) adduct of trimethylol propane in an amount corresponding to 0.6 equivalent of the hydroxyl group of the polymer (B) (Nippon Polyurethane Co., trade name " Coronate L ") was added. Finally, 2.0 parts by mass of N-butyl-4-methylpyridinium hexafluorophosphite as the antistatic agent (D) and 3 parts by mass of 3-glycidoxypropylmethoxysilane (trade name, available from Shin- &Quot; KBM403 ") were added, and sufficiently stirred to obtain a diluted solution of the adhesive composition.

Table 1 shows the composition of the adhesive composition. The abbreviations listed in Table 1 are as follows.

[Polymers (A) and (B)]

BA: n-butyl acrylate

AA: Acrylic acid

MA: methacrylic acid

MEA: 2-methoxyethyl acrylate

HEA: Acrylic acid-hydroxyethyl

4HBA: Acrylic acid-hydroxybutyl

PhEA: phenoxyethyl acrylate

[Isocyanate crosslinking agent (C)]

Colonate L: Tolylene diisocyanate adduct of trimethylol propane (trade name " Colonate L ", trade name, manufactured by Nippon Polyurethane Industry Co., Ltd.)

Colonate HX: hexamethylene diisocyanate isocyanurate (trade name: Colonate HX, manufactured by Nippon Polyurethane Industry Co., Ltd.)

Dyuranate 24A-100: Hexamethylene diisocyanate-based buret (Dyuranate 24A-100, manufactured by Asahi Chemical Industry Co., Ltd.)

[Antistatic agent (D)]

Pyridinium: N-butyl-4-methylpyridinium hexafluorophosphite

KFSI: Mixed solution of bis (fluorosulfonylimide) potassium (KFSI): tetraglyme = 1: 1 (mass ratio) * The blending amount in the table is KFSI only

LiTFSI: Mixed solution of bis (trifluoromethanesulfonylimide) lithium (LiTFSI): tetraglyme = 1: 1 (ratio by mass) * The amounts in the table are values only for LiTFSI

AS-804: Daiichi Kyoei Co., Ltd., onium salt antistatic agent, trade name "AS-804"

[Silane coupling agent (E)]

KBM403: 3-glycidoxypropylmethoxysilane (trade name: KBM403, manufactured by Shin-Etsu Chemical Co., Ltd.)

KBE9007: 3-isocyanate propyltriethoxysilane (trade name: KBE9007, manufactured by Shin-Etsu Chemical Co., Ltd.)

X-41-1059A: An oligomer-based silane coupling agent (trade name "X-41-1059A", manufactured by Shinetsu Kagaku Co., Ltd.)

The diluted solution of the obtained sticky composition was applied to a release surface of a release sheet (SP-PET3811, thickness: 38 m, manufactured by LINTEC CO., LTD.) In which one surface of the polyethylene terephthalate film was peeled off with a silicone- , And then heat-treated at 90 DEG C for 1 minute to form a pressure-sensitive adhesive layer.

Then, a polarizing plate composed of a polarizing film with a discotic liquid crystal layer and an integrated polarizing film and a viewing angle enlarging film was laminated so that the exposed surface of the pressure sensitive adhesive layer and the surface of the discotic liquid crystal layer were in contact with each other, RH for 7 days to obtain a polarizing plate with a pressure-sensitive adhesive layer.

[Examples 2 to 26, Comparative Examples 1 to 3]

(A) and the polymer (B) were changed as shown in Table 1, in addition to changing the kind and proportion of each monomer constituting the adhesive composition, the kind and amount of the crosslinking agent, the antistatic agent and the silane coupling agent, 1, a polarizer with a pressure-sensitive adhesive layer was prepared.

Here, the weight average molecular weight (Mw) described above is a weight average molecular weight in terms of polystyrene measured by gel permeation chromatography (GPC) under the following conditions (GPC measurement).

<Measurement Conditions>

· GPC measuring apparatus: HLC-8020 manufactured by Tosoh Corporation

· GPC column (pass in the following order): TOSOH Corporation

  TSK guard column HXL-H

  TSK gel GMHXL (× 2)

  TSK gel G2000 HXL

Measurement solvent: tetrahydrofuran

· Measuring temperature: 40 ℃

Using a release sheet (SP-PET3801, manufactured by LINTEC Co., Ltd., thickness: 38 mu m) obtained by replacing the polarizing plate used in the production of the polarizing plate with a pressure-sensitive adhesive layer in Example or Comparative Example and peeling the one side of the polyethylene terephthalate film with a silicone- To prepare a pressure-sensitive adhesive sheet. Specifically, the peeling sheet was laminated on the pressure-sensitive adhesive layer on which the constitution made of the release sheet / pressure-sensitive adhesive layer (thickness: 25 m) obtained in the manufacturing process of the example or the comparative example was exposed. Thus, a pressure-sensitive adhesive sheet having a configuration of a release sheet / pressure-sensitive adhesive layer / release sheet was produced.

The obtained pressure-sensitive adhesive sheet was cured for 7 days under conditions of 23 캜 and 50% RH. Thereafter, the pressure-sensitive adhesive sheet was sampled at a size of 80 mm x 80 mm, the pressure-sensitive adhesive layer was surrounded by a mesh made of polyester (mesh size 200), and the mass of the pressure-sensitive adhesive alone was measured with a precision balance. The mass at this time is denoted by M1.

Next, the pressure sensitive adhesive surrounded by the polyester mesh was immersed in ethyl acetate at room temperature (23 DEG C) for 24 hours. Thereafter, the pressure-sensitive adhesive was taken out, ventilated and dried for 24 hours under an environment of a temperature of 23 ° C and a relative humidity of 50%, and further dried in an oven at 80 ° C for 12 hours. The mass of the adhesive after drying was measured with a precision scale. The mass at this time is M2. The gel fraction (%) is expressed by (M2 / M1) x100. The results are shown in Table 2.

[Test Example 2] (Light leakage test)

The polarizing plate with a pressure-sensitive adhesive layer obtained in Example or Comparative Example was adjusted to a size of 233 mm x 309 mm by using a cutting device (super cutter, manufactured by Oginosei Co., Ltd., PN1-600). The peeled sheet was peeled off and attached to a non-alkali glass (Eagle XG, made by Corning) through the exposed pressure-sensitive adhesive layer, followed by pressurization at 0.5 MPa and 50 deg. C for 20 minutes in an autoclave made by Kurihara Seisakusho. On the other hand, the above bonding was carried out so that the polarization axis of the polarizing plate with a pressure-sensitive adhesive layer was in the cross-Nicol state (polarizing axis: angle 45 deg., Angle 135 deg.) On the front and back of the alkali-free glass. In this state, the sample was allowed to stand in an 80 ° C. dry environment for 250 hours, and then left for 2 hours in an environment of 23 ° C. and 50% RH. Using this sample as a sample, the light leakage property was evaluated by the following method. The results are shown in Table 2.

<Evaluation of light leakage property:? L ^* >

Using the MCPD-2000 manufactured by Otsuka Chemical Co., Ltd., the lightness (L ^* ) of each area shown in Fig. 3 in the sample was measured, and the lightness difference? L ^*

? L ^* = [(b + c + d + e) / 4] -a

(Where a, b, c, d and e are brightness values at predetermined measurement points (one central portion of each region) of the A region, B region, C region, D region and E region) Light leakage. The smaller the value of? L ^*, the smaller the light leakage.

[Test Example 3] (Evaluation of durability)

The polarizing plate with a pressure-sensitive adhesive layer obtained in Example or Comparative Example was adjusted to a size of 233 mm x 309 mm by using a cutting device (super cutter, manufactured by Oginosei Co., Ltd., PN1-600). The peeled sheet was peeled off and attached to an alkali-free glass (Eagle XG, manufactured by Corning) through the exposed pressure-sensitive adhesive layer, followed by pressurization at 0.5 MPa and 50 캜 for 20 minutes in an autoclave made by Kurihara Seisakusho.

Thereafter, the cells were placed under the conditions of the following durability conditions, and observation was carried out using a 10-fold magnifier after 500 hours. The appearance change was based on the following. The results are shown in Table 2.

◎: On four sides, without defect

○: On four sides, there are no defects in the area of 0.6 mm or more from the peripheral edge

X: At least one side of four sides, at least 0.6 mm from the outer peripheral end, has appearance defects such as peeling, peeling, foaming, streaking or the like of a pressure-sensitive adhesive of 0.1 mm or more

 &Lt; Durability condition &

· 80 ° C dry

· 60 ℃, relative humidity 90% RH

[Test Example 4] (Measurement of adhesive force)

The polarizing plate with a pressure-sensitive adhesive layer obtained in Examples or Comparative Examples was cut to produce samples having a width of 25 mm and a length of 100 mm. The release sheet was peeled off from the sample, and the sample was stuck to a non-alkali glass (Eagle XG, made by Corning) through the exposed pressure-sensitive adhesive layer. Then, the sample was transferred to an autoclave of Kurihara Seisakusho Co., Lt; / RTI &gt; Thereafter, the film was allowed to stand under the conditions of 23 ° C. and 50% RH for 24 hours, and then the adhesive strength was measured using a tensile tester (Tensilon manufactured by Orientec Co., Ltd.) at a peeling speed of 300 mm / min and a peeling angle of 180 ° (N / 25 mm) was measured. The results are shown in Table 2.

[Test Example 5] (Measurement of surface resistance value)

The polarizing plate with a pressure-sensitive adhesive layer obtained in Example or Comparative Example was cut into a size of 50 mm x 50 mm, and the obtained sample was left for 24 hours at a temperature of 23 캜 and a humidity of 50% RH. Thereafter, the release sheet was peeled off and the surface resistance value (Ω / sq) was measured according to JIS K6911 using a resistivity meter (Hirestor UP MCP-HT450 type, manufactured by Mitsubishi Chemical Corp.) Respectively. The results are shown in Table 2.

As can be seen from Table 2, the polarizing plate with a pressure-sensitive adhesive layer obtained in the examples had sufficient adhesion and antistatic properties, exhibited excellent stress relaxation properties, and excellent both of light resistance leak resistance and durability.

The pressure-sensitive adhesive composition and pressure-sensitive adhesive of the present invention are suitable for bonding optical members such as a polarizing plate and a retardation plate, and the pressure-sensitive adhesive sheet of the present invention is suitable as a pressure-sensitive adhesive sheet for optical members such as a polarizing plate and a retardation plate.

1A, 1B ... Adhesive sheet
11 ... The pressure-
12, 12a, 12b ... Peeling sheet
13 ... materials

Claims (14)

A first (meth) acrylic acid ester polymer (A) having a weight average molecular weight of 500,000 to 3,000,000,
A second (meth) acrylic acid ester polymer (B) having a weight average molecular weight of 8000 to 300000,
A cross-linking agent (C)
An antistatic agent (D) is contained,
The ratio of the second (meth) acrylic acid ester polymer (B) to 100 parts by mass of the first (meth) acrylic acid ester polymer (A) is 5 to 50 parts by mass,
The second (meth) acrylic acid ester polymer (B) contains a monomer having a functional group (b1) reacting with the crosslinking agent (C) as a constituent component, and the ratio of the monomer having the functional group , And more than 1% by mass and less than 50% by mass in the second (meth) acrylic acid ester polymer (B)
Wherein the first (meth) acrylic acid ester polymer (A) contains no monomer having a functional group which reacts with the crosslinking agent (C) as a constituent, or the functional group of the second (meth) acrylic acid ester polymer (B) (a1) having a lower reactivity with the crosslinking agent (C) than the crosslinking agent (b1)
The first (meth) acrylic acid ester polymer (A) or the first (meth) acrylic acid ester polymer (A) and the second (meth) acrylic acid ester polymer (B) By mass of an oxyalkylene group-containing monomer in an amount of 5 to 50% by mass. delete A first (meth) acrylic acid ester polymer (A) having a weight average molecular weight of 500,000 to 3,000,000,
A second (meth) acrylic acid ester polymer (B) having a weight average molecular weight of 8000 to 300000,
A cross-linking agent (C)
An antistatic agent (D) is contained,
The ratio of the second (meth) acrylic acid ester polymer (B) to 100 parts by mass of the first (meth) acrylic acid ester polymer (A) is 5 to 50 parts by mass,
The second (meth) acrylic acid ester polymer (B) contains a monomer having a functional group (b1) reacting with the crosslinking agent (C) as a constituent component, and the ratio of the monomer having the functional group , And more than 1% by mass and less than 50% by mass in the second (meth) acrylic acid ester polymer (B)
Wherein the first (meth) acrylic acid ester polymer (A) contains no monomer having a functional group which reacts with the crosslinking agent (C) as a constituent, or the functional group of the second (meth) acrylic acid ester polymer (B) (a1) having a lower reactivity with the crosslinking agent (C) than the crosslinking agent (b1)
The antistatic agent (D) is an ionic compound. The method of claim 3,
Wherein the ionic compound is at least one member selected from the group consisting of a nitrogen-containing onium salt, a sulfur-containing onium salt, a phosphorus-containing onium salt, an alkali metal salt and an alkaline earth metal salt. The method of claim 4,
Wherein the alkali metal salt is at least one selected from the group consisting of a lithium salt and a potassium salt. The method according to claim 1 or 3,
The functional group (a1) in the first (meth) acrylic acid ester polymer (A) is a carboxyl group,
The functional group (b1) in the second (meth) acrylic acid ester polymer (B) is a hydroxyl group,
Wherein the cross-linking agent (C) is an isocyanate-based cross-linking agent. The method according to claim 1 or 3,
The first (meth) acrylic acid ester polymer (A) contains no carboxyl group-containing monomer as the monomer unit constituting the polymer, or contains a carboxyl group-containing monomer as the functional group (a1) in an amount of 15 mass% or less By weight. The method according to claim 1 or 3,
Wherein the second (meth) acrylic acid ester polymer (B) contains 3 to 40 mass% of a hydroxyl group-containing monomer as the functional group (b1). The method of claim 6,
The content of the isocyanate crosslinking agent is such that the isocyanate group of the isocyanate crosslinking agent is 0.1 to 3.5 equivalents based on the amount of the functional group (b1) in the second (meth) acrylic acid ester polymer (B). Composition. A pressure-sensitive adhesive comprising the pressure-sensitive adhesive composition according to claim 1 or 3 crosslinked. The method of claim 10,
Wherein a surface resistivity of the pressure-sensitive adhesive is 3.0 x 10 &lt; ¹¹ &gt; OMEGA / sq or less. A pressure-sensitive adhesive sheet comprising a substrate and a pressure-sensitive adhesive layer,
The pressure-sensitive adhesive sheet according to claim 10, wherein the pressure-sensitive adhesive layer comprises the pressure-sensitive adhesive according to claim 10. The method of claim 12,
Wherein the substrate is an optical member. Two release sheets,
And a pressure-sensitive adhesive layer sandwiched between the release sheets so as to come into contact with the release surfaces of the two release sheets,
The pressure-sensitive adhesive sheet according to claim 10, wherein the pressure-sensitive adhesive layer comprises the pressure-sensitive adhesive according to claim 10.

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