JP4521522B2 - Optical member and manufacturing method thereof - Google Patents

Description

  The present invention relates to an optical member that is highly durable even when used in a large-screen liquid crystal device, and that hardly leaks light, and a method of manufacturing the optical member.

  Conventionally, an optical member such as a polarizing plate or a retardation plate has been used in a liquid crystal display device or the like. Such an optical member is composed of a base film having desired optical characteristics and an adhesive layer provided on the surface of the base film, and the desired optical material is formed on the surface of the glass substrate of the liquid crystal element via the adhesive layer. A base film having optical properties is attached and used. The liquid crystal display devices as described above are used in a very wide range of fields, and there are very severe use conditions in such applications, and foaming, swelling or peeling is also caused under high temperature and high humidity conditions. In order not to occur, the adhesive layer of the optical member is required to have high durability.

  In order to improve the durability of the pressure-sensitive adhesive layer, conventionally, a method has been adopted in which a three-dimensional cross-linked structure is formed in the pressure-sensitive adhesive layer to develop strength in the pressure-sensitive adhesive layer itself. That is, for example, an acrylic adhesive having a functional group such as a hydroxyl group is mixed with an epoxy compound, a polyisocyanate compound, etc. as a crosslinking agent, and an adhesive layer is formed to connect acrylic adhesive molecules to each other. The structure is improved and the durability of the entire pressure-sensitive adhesive layer is improved. By forming the three-dimensional crosslinked structure in this way, the gel fraction of the component forming the pressure-sensitive adhesive layer is increased and the durability is increased. However, as the gel fraction increases, the light from the pressure-sensitive adhesive layer is increased. Leakage is likely to occur.

  Such light leakage is not so much a problem in a small-screen liquid crystal display device, but in a large-screen liquid crystal display device exceeding 20 inches, for example, a uniform luminance is required over the entire screen, and polarization The light leakage of an optical member such as a plate is a very big problem. In order to prevent such light leakage, the gel fraction of the component forming the pressure-sensitive adhesive layer may be lowered. However, in order to improve the durability of the pressure-sensitive adhesive layer of the conventional optical member, the pressure-sensitive adhesive layer is formed. It was necessary to increase the gel fraction of the component, and the durability and light leakage of the pressure-sensitive adhesive layer could not be satisfied at the same time.

For example, Patent Document 1 (Japanese Patent Application Laid-Open No. 07-082542) discloses an invention relating to an adhesive for a polarizing plate or a retardation plate employed in a liquid crystal display panel. This pressure-sensitive adhesive is a graft or block copolymer having a total molecular weight of 400,000 to 2 million, having two types of Tg peaks, and having a Tg difference of 50 ° C. or more, and exhibiting a high Tg. Is composed of any one of styrene, acrylonitrile, methyl methacrylate homopolymer or copolymer, polyester, and polyamide, the molecular weight of this segment is in the range of 500 to 1,000,000, and this segment is 5 to 40 wt. % Of the pressure-sensitive adhesive is disclosed. That is, in this Patent Document 1, butyl allylate is copolymerized with acrylic acid, 2-hydroxyethyl acrylate, and a styrene macromonomer having a vinyl group at the end (molecular weight of about 10,000), and 89 ° C. and −43 A pressure-sensitive adhesive composition is disclosed in which a copolymer having two glass transition temperatures of 0 ° C. is produced, and the polyisocyanate compound Coronate L is added to the copolymer. The high-temperature glass transition temperature of this copolymer corresponds to the glass-transition temperature of the segment composed of styrene macromonomer, and the low-temperature glass transition temperature is a segment formed from butyl allylate, acrylic acid, 2-hydroxyethyl acrylate. It almost corresponds to the glass transition point of.

However, since the polyisocyanate compound reacts with a hydroxyl group derived from 2-hydroxyethyl acrylate to form a three-dimensional cross-linked structure between the molecules in the pressure-sensitive adhesive described in this reference 1, this pressure-sensitive adhesive is used. The gel fraction of the agent is about 50% by weight. Thus, since the adhesive described in the cited document 1 has a high gel fraction, light leakage is likely to occur and it cannot be used as an adhesive for a polarizing plate used in a large-screen liquid crystal display device. .

Patent Document 2 (Japanese Patent Laid-Open No. 09-113724) discloses an acrylic copolymer (A) having no hydroxyl group and an acrylic copolymer (B) having a hydroxyl group from 20:80 to An invention of an adhesive polarizing plate is disclosed in which a composition containing 50:50 is attached with an acrylic adhesive that is crosslinked with 0.3 to 5 parts by weight of a polyfunctional isocyanate compound (C).

However, the pressure-sensitive adhesive described in Patent Document 2 has a crosslinked structure formed of the polyfunctional isocyanate compound (C), and the gel fraction thereof is about 70% by weight. Therefore, the polarizing plate having the pressure-sensitive adhesive layer in which the cross-linked structure is formed as the gel fraction becomes higher tends to cause light leakage and cannot be used for a large-screen liquid crystal display device.
Japanese Unexamined Patent Publication No. 07-082542 JP 09-113724 A

  An object of the present invention is to provide an optical member that has sufficient durability and is less likely to cause light leakage, and a method for manufacturing the optical member.

The optical member of the present invention is
(A) The glass transition temperature is −60 ° C. to −30 ° C., the weight average molecular weight is 1.2 million to 2 million, and the copolymerization amount of the monomer containing a functional group capable of reacting with the curing agent is 0 to 0. A low Tg (meth) acrylic polymer that is 5% by weight ;
(B) The glass transition temperature is 20 ° C. to 80 ° C., the weight average molecular weight is 500,000 to 2,000,000 , and the copolymerization amount of the monomer containing a functional group capable of reacting with the curing agent is 6% by weight to 20%. High Tg (meth) acrylic polymer in weight percent ; 1-15 parts by weight;
(C) at least one curing agent selected from the group consisting of epoxy curing agents, amine curing agents and metal chelate compound curing agents; 0.003 to 0.5 parts by weight;
(D) a polyisocyanate compound; a composition containing 0.5 to 3 parts by weight,
It is characterized in that a pressure-sensitive adhesive layer that has been aged so as to have a gel fraction of less than 30% by weight in an environment having humidity is formed on the surface of the substrate.

Furthermore, the manufacturing method of the optical member of the present invention includes:
(A) The glass transition temperature is −60 ° C. to −30 ° C., the weight average molecular weight is 1.2 million to 2 million, and the copolymerization amount of the monomer containing a functional group capable of reacting with the curing agent is 0 to 0. A low Tg (meth) acrylic polymer that is 5% by weight ;
(B) The glass transition temperature is 20 ° C. to 80 ° C., the weight average molecular weight is 500,000 to 2,000,000 , and the copolymerization amount of the monomer containing a functional group capable of reacting with the curing agent is 6% by weight to 20%. High Tg (meth) acrylic polymer in weight percent ; 1-15 parts by weight;
(C) a curing agent selected from the group consisting of epoxy curing agents, amine curing agents and metal chelate compound curing agents; 0.003 to 0.5 parts by weight;
(D) a polyisocyanate compound; a composition containing 0.5 to 3 parts by weight,
It is characterized by aging such that the gel fraction of the pressure-sensitive adhesive layer is less than 30% by weight in an environment having humidity.

In the present invention, the (C) curing agent mainly forms an intramolecular crosslinked structure with the functional group present in the (B) high Tg (meth) acrylic polymer. Therefore, the gel fraction after aging (adhesive after the formation of a crosslinked structure) is also less than 30% by weight, and in many cases, 10% by weight or less. Also these (
C) Compared with the reactivity of the curing agent, (D) the polyisocyanate compound has a low reactivity with the functional group in the (B) high Tg (meth) acrylic polymer, and in the presence of (C) the curing agent, The reaction with the curing agent (C) takes precedence over the reaction with the (D) polyisocyanate compound. In addition, polyisocyanate compounds are known to absorb water in the environment and to multimerize, and in the aging process having humidity as employed in the present invention, the water absorbs moisture contained in the air. Multimerize. For example, when the pressure-sensitive adhesive forming the pressure-sensitive adhesive layer of the optical member of the present invention after aging is measured by GPC, a peak (a molecular weight of, for example, about 1400) that a polyisocyanate compound is thought to be multimerized is observed, This substantially coincides with the molecular weight of the polyisocyanate compound that has been multimerized (for example, dimerized). Therefore, in the optical member of the present invention, (C) the curing agent forms an intramolecular crosslinked structure in (B) a high Tg (meth) acrylic polymer, and (D) the polyisocyanate compound is in an aging environment. It is considered that a certain amount of water is absorbed and multimerized to restrain the movement of the (A) low Tg (meth) acrylic polymer. Therefore, the pressure-sensitive adhesive layer formed on the optical member of the present invention is excellent even though the gel fraction is less than 30% by weight, and preferably the gel fraction is substantially close to 0% by weight. In addition to having a high durability, it has a characteristic that light leakage from the pressure-sensitive adhesive layer hardly occurs.

The optical member of the present invention comprises a substrate and a pressure-sensitive adhesive layer formed on the surface. The pressure-sensitive adhesive layer comprises a specific (A) low Tg (meth) acrylic polymer and a specific high glass transition point. Using a composition comprising a (meth) acrylic polymer, a crosslinking agent, and a polyisocyanate compound, a specific (
B) A cross-linked structure is selectively formed in the molecule of the high Tg (meth) acrylic polymer, and (A)
The entangled portion of the low Tg (meth) acrylic polymer molecule is a polymer of (D) polyisocyanate compound, and the gel fraction of the pressure-sensitive adhesive forming the pressure-sensitive adhesive layer by binding to each other is less than 30% by weight. Yes. That is, in the pressure-sensitive adhesive layer constituting the optical member of the present invention, a crosslinked structure is formed at a low crosslinking density in the molecule of (B) a high Tg (meth) acrylic polymer, but (A) a low Tg There is almost no crosslinked structure formed between the molecules of the (meth) acrylic polymer and between the molecules of the (B) high Tg (meth) acrylic polymer and the (A) low Tg (meth) acrylic polymer, In addition, the entangled portion of the (A) low Tg (meth) acrylic polymer is a polymer of a polyisocyanate compound (
It is thought that molecules are usually bound by a dimer or more). Therefore, when the gel fraction is measured about the adhesive which forms the adhesive layer of the optical member of this invention, the gel fraction of an adhesive layer formation component is less than 30 weight%.

  In general, a pressure-sensitive adhesive having a gel fraction of less than 30% by weight indicates that a three-dimensional cross-linking structure sufficient as a pressure-sensitive adhesive is not formed, and the movement of the pressure-sensitive adhesive cannot be controlled. As in the present invention, (B) a cross-linked structure is formed in the molecule of the high Tg (meth) acrylic polymer, and (A) the intermolecular molecules of the low Tg (meth) acrylic polymer are formed by a multimer of polyisocyanate compounds. By binding, movement of the pressure-sensitive adhesive component in the pressure-sensitive adhesive layer can be controlled.

  As a result, the optical member of the present invention has sufficient durability despite the low gel fraction of the pressure-sensitive adhesive layer, and whether a three-dimensional cross-linked structure is hardly formed between the molecules. Alternatively, even when intermolecular cross-linking is performed, a high molecular weight body that generates a gel fraction is hardly formed. Therefore, the followability (form followability) is excellent, and light leakage does not occur.

  Therefore, the optical member of the present invention can be used as a polarizing plate or a retardation plate of a liquid crystal display device having a large screen exceeding 20 inches, for example.

Next, the optical member of the present invention and the manufacturing method thereof will be specifically described.
The optical member of the present invention has a base material and an adhesive layer formed on the surface of the base material.
In the optical member of the present invention, the pressure-sensitive adhesive layer comprises a low Tg (meth) acrylate polymer (A), a high Tg (meth) acrylate polymer (B), a curing agent (C), and a polyisocyanate compound (D). Can be formed by aging in a humid environment.

The low Tg (meth) acrylate polymer (A) that can be used in the present invention is:
A (meth) acrylate polymer having a glass transition temperature of −30 ° C. or lower, preferably in the range of −30 ° C. to −60 ° C. When a polymer having a glass transition temperature (Tg) higher than −30 ° C. is used as the low Tg (meth) acrylate polymer (A), the light leakage resistance of the formed adhesive layer deteriorates and removability (rework) ) Is inferior.

Furthermore, the weight average molecular weight (Mw) of the low Tg (meth) acrylate polymer (A) is 12
It is 100,000 or more, preferably in the range of 1.2 million to 2 million. When the weight average molecular weight (Mw) of the low Tg (meth) acrylate polymer (A) is less than 1.2 million, the durability of the formed adhesive layer is inferior. In the present invention, the weight average molecular weight (Mw) of the polymer is a value measured by gel permeation chromatography (GPC).

  The low Tg (meth) acrylate polymer (A) as described above is an acrylic polymer formed by (co) polymerizing a (meth) acrylic compound so that the glass transition temperature is −30 ° C. or lower. In this low Tg (meth) acrylate polymer (A), the amount of the monomer containing a functional group capable of reacting with the curing agent (C) used in the present invention is 0.5% by weight or less, preferably 0 to 0%. It may be copolymerized in an amount within the range of 0.3% by weight. That is, the low Tg (meth) acrylate polymer (A) of the present invention has an alkyl (meth) acrylate (co-polymerized) in which the alkyl (meth) acrylate is (co) polymerized so that the glass transition temperature (Tg) is −30 ° C. or lower. ) A polymer, or a copolymer of an alkyl (meth) acrylate and a monomer containing a functional group capable of reacting with the curing agent (C).

  As a monomer for forming the low Tg (meth) acrylate polymer used in the present invention, a monomer having a glass transition temperature (Tg) of the (co) polymer of −30 ° C. or less is used alone or in combination. Can do. As an example of such a monomer, it is preferable to use a (meth) acrylate compound having an alkyl group having 1 to 18, preferably 3 to 18 carbon atoms in the alkyl group. This alkyl group is preferably linear. When the alkyl group has a branch, the alkyl group becomes sterically hindered, and the polyisocyanate compound multimer reduces the low Tg (meth) acrylate polymer (A). There is a risk of being restrained. In the present invention, the monomer composition is selected so that the glass transition temperature (Tg) of the (co) polymer forming the low Tg (meth) acrylate polymer is -30 ° C. or lower.

Preferable examples of the monomer forming the low Tg (meth) acrylate polymer (A) include n-butyl (meth) acrylate, n-pentyl (meth) acrylate, n-hexyl (meth) acrylate, n-octyl ( (Meth) having an alkyl group having 4 to 8 carbon atoms such as (meth) acrylate
Mention may be made of acrylates. Further, the low Tg (meth) acrylate polymer used in the present invention can react with the curing agent (C) in an amount of 0.5% by weight or less, preferably 0 to 0.3% by weight. Monomers having functional groups may be copolymerized, and examples of such functional group-containing monomers include carboxyl group-containing monomers such as (meth) acrylic acid, itaconic acid, crotonic acid, and maleic acid. it can. If the copolymerization amount of the functional group-containing monomer in the low Tg (meth) acrylate polymer is small as described above, the reaction between the curing agent (C) or the polyisocyanate compound (D) and this functional group hardly occurs. Therefore, a three-dimensional crosslinked structure that causes light leakage is not formed. When the copolymerization amount of the monomer having a functional group capable of reacting with the curing agent (C) in the low Tg (meth) acrylate polymer exceeds 0.5% by weight, light leakage of the formed adhesive layer is likely to occur. Become. This low Tg (
The meth) acrylate polymer is desirably one that does not react with the isocyanate compound, and therefore preferably does not contain a highly reactive functional group such as a hydroxyl group or an amino group that easily reacts with the isocyanate compound.

  The low Tg (meth) acrylate polymer (A) as described above has good adhesiveness, but if stress continues to be applied in the sticking state, a shift occurs between the molecules, and this is caused by the shift of the molecules. The cohesive strength should not be high. Moreover, since this low Tg (meth) acrylate polymer (A) has a gel fraction of substantially 0% by weight and cannot form a strong adhesive layer by itself, this low Tg (meth) acrylate polymer ( A) alone cannot exhibit the durability required for the pressure-sensitive adhesive layer of the optical member.

A high Tg (meth) acrylate polymer (B) is used as a component for forming the pressure-sensitive adhesive layer of the optical member of the present invention.
The high Tg (meth) acrylate polymer (B) forming the pressure-sensitive adhesive layer of the optical member of the present invention has a (meth) acrylic system so that the glass transition temperature (Tg) is 20 ° C. or higher, preferably 20 to 80 ° C. It is a polymer in which a monomer having a functional group capable of reacting with the compound and the curing agent (C) is copolymerized within a range of 6% by weight or more, preferably 10 to 20% by weight. Further, the high Tg (meth) acrylate polymer (B) has a weight average molecular weight of 500,000 or more, preferably in the range of 500,000 to 2,000,000.

The high Tg (meth) acrylate polymer (B) usually contains a (meth) acrylate having an alkyl group having 1 to 18 carbon atoms, preferably 1 to 12 carbon atoms, and a functional group capable of reacting with the curing agent (C). It is a copolymer with the monomer to be used. The (meth) acrylate used here is methyl (meth) acrylate, ethyl (meth) acrylate, n-propyl (meth) acrylate, iso-propyl (meth) acrylate, n-butyl (meth) acrylate, tert-butyl (Meth) acrylate, iso-butyl (meth) acrylate and the like can be mentioned.

  Examples of the monomer containing a functional group capable of reacting with the curing agent (C) forming the high Tg (meth) acrylate polymer (B) include carboxyl group-containing (meth) acrylic such as acrylic acid and methacrylic acid. -Based monomers, amino group-containing (meth) acrylic monomers such as N, N-dimethylaminoethyl (meth) acrylate, and amide group-containing (meth) acrylic monomers such as (meth) acrylamide and N-methylacrylamide be able to.

  In the high Tg (meth) acrylate polymer (B), the copolymerization amount of the monomer containing a functional group capable of reacting with the curing agent (C) is 6% by weight or more, preferably 10 to 20% by weight. %. When the copolymerization amount of the monomer containing a functional group capable of reacting with the curing agent (C) is less than 6% by weight, the durability of the pressure-sensitive adhesive layer in the optical member of the present invention is poor. However, the high Tg (meth) acrylate polymer (B) mainly forms an intramolecular cross-linked structure with the curing agent (C) described later, and hardly forms an intermolecular cross-linked structure or is inter-molecular cross-linked. However, since it hardly forms a three-dimensional cross-linking structure that generates a gel fraction, it is desirable that the polyisocyanate compound such as a hydroxyl group does not have a functional group having high activity.

In the present invention, the high Tg (meth) acrylate polymer (B) is in an amount within the range of 1 to 15 parts by weight, preferably 4 to 10 parts by weight with respect to 100 parts by weight of the low Tg (meth) acrylate polymer (A). Used in part quantities. When the amount of the high Tg (meth) acrylate polymer (B) used is less than 1 part by weight, the durability of the formed pressure-sensitive adhesive layer is inferior, and when it exceeds 15 parts by weight, the high Tg (meth) acrylate polymer is used. (B) A large amount of cross-linking between molecules occurs, and the followability (form followability) decreases, so that light leakage tends to occur in the formed pressure-sensitive adhesive layer.

  The curing agent (C) blended in the composition forming the pressure-sensitive adhesive layer of the optical member of the present invention reacts with the functional group introduced in the high Tg (meth) acrylate polymer (B) to cause intramolecular crosslinking. In the present invention, any one of an epoxy curing agent, an amine curing agent and a metal chelate compound curing agent is used as the curing agent (C).

Examples of the epoxy curing agent used as the curing agent (C) in the present invention include N, N, N ′, N′-tetraglycidyl-m-xylenediamine, bisphenol A, and polyethylene glycol glycidyl ether. Examples of amine curing agents include N, N, N ′, N′-tetramethylhexamethylenediamine, and examples of metal chelate compound curing agents include Al and Ni. And metal compounds such as Zn. These curing agents (C) can be used alone or in combination. In particular, in the present invention, it is preferable to use an epoxy curing agent.

  In the present invention, the curing agent (C) is in an amount within the range of 0.003 to 0.5 parts by weight, preferably 0.01 to 0.3 parts per 100 parts by weight of the low Tg (meth) acrylate polymer (A). Use in an amount within the range of parts by weight. This curing agent (C) must be in an amount sufficient to react with the functional group introduced into the high Tg (meth) acrylate polymer (B) to form an intramolecular crosslinked structure. If the amount is less than 0.003 parts by weight, an intramolecular crosslinked structure sufficient to impart sufficient durability to the pressure-sensitive adhesive layer cannot be formed, and if more than 0.5 parts by weight, An inter-crosslinked structure is formed, and the gel fraction of the formed pressure-sensitive adhesive layer cannot be controlled to be less than 30% by weight, so that the light leakage resistance becomes insufficient.

A polyisocyanate compound (D) is blended in the composition forming the pressure-sensitive adhesive layer of the optical member of the present invention.
Examples of the polyisocyanate compound (D) used in the present invention include tolylene diisocyanate, xylene diisocyanate, hexamethylene diisocyanate, and adducts thereof with polyols such as trimethylolpropane. These can be used alone or in combination. In the present invention, the polyisocyanate compound (D) is polymerized by absorbing moisture in the air by aging under conditions containing moisture. Among the polyisocyanate compounds described above, an adduct with a polyol is used. It is preferable to use the body.

  In the present invention, the polyisocyanate compound (D) is used in an amount in the range of 0.5 to 3 parts by weight, preferably 1.0 to 3.0 parts by weight, with respect to 100 parts by weight of the low Tg (meth) acrylic polymer. Used in quantities within the range of parts.

  This polyisocyanate compound (D) absorbs moisture in the air during aging and multimerizes to form a low Tg (meth) acrylate polymer (A) at the entangled portion of the low Tg (meth) acrylate polymer (A) molecule. It seems to restrain the migration of the low Tg (meth) acrylate polymer (A) molecule by restraining the molecule. If the polyisocyanate compound (D) is not used, the durability of the pressure-sensitive adhesive layer to be formed, particularly the high temperature durability, will be insufficient.

If necessary, the composition forming the pressure-sensitive adhesive layer of the optical member of the present invention may contain a silane coupling agent (E).
Examples of the silane coupling agent (E) used in the present invention include polymerizable unsaturated group-containing silicon compounds such as vinylmethoxysilane, epoxy group-containing silicon compounds such as 3-glycidoxypropylmethoxysilane, 3- Examples thereof include amino group-containing silicon compounds such as aminopropylmethoxysilane.

In the present invention, the silane coupling agent (E) is the low Tg (meth) acrylic polymer 10
It is usually used in an amount in the range of 0.05 to 5 parts by weight, preferably in an amount in the range of 0.1 to 3 parts by weight relative to 0 part by weight. By using the silane coupling agent (E) in such an amount, the durability of the formed pressure-sensitive adhesive layer is improved.

  In the present invention, the low Tg (meth) acrylate polymer (A) and the high Tg (meth) acrylate polymer (B) as described above are produced separately, and the low Tg (meth) acrylate polymer (A ) And a high Tg (meth) acrylate polymer (B) are mixed in a predetermined ratio, and then a predetermined amount of a curing agent (C), a polyisocyanate compound (D), and a silane coupling agent (E) if necessary are mixed. Then, a composition for coating is prepared. The low Tg (meth) acrylate polymer (A) and the high Tg (meth) acrylate polymer (B) can control the weight average molecular weight by appropriately adjusting the type of polymerization initiator, reaction solvent, reaction temperature, and the like. it can. For example, by using ethyl acetate as a reaction solvent and setting the reaction temperature relatively low, a polymer having a high weight average molecular weight can be produced. For example, a mixed reaction solvent of ethyl acetate and toluene is used. By doing so, the reaction temperature can be increased to produce a polymer having a low weight average molecular weight.

Further, the glass transition temperature (Tg) of the low Tg (meth) acrylate polymer (A) and the high Tg (meth) acrylate polymer (B) has a (meth) acrylate having an alkyl group and a functional group. By adjusting the copolymerization ratio with the monomer, the glass point transition temperature of the resulting polymer can be calculated based on the Fox equation.

An organic solvent solution containing a low Tg (meth) acrylate polymer (A) and an organic solvent solution containing a high Tg (meth) acrylate polymer (B), which are individually produced as described above, Are mixed so that the amount ratio is as described above. In this case, the organic solvent solution containing the low Tg (meth) acrylate polymer (A) and the organic solvent solution containing the high Tg (meth) acrylate polymer (B) may be used by separating the polymer from the reaction solvent. The reaction solution dissolved or dispersed in the reaction solvent may be used as it is. The mixture containing the low Tg (meth) acrylate polymer (A) and the high Tg (meth) acrylate polymer (B) as described above. A coating composition is prepared by adding the curing agent (C) and the polyisocyanate compound (D) to the silane coupling agent (E) as necessary. This coating composition is usually mixed at a temperature around room temperature. The viscosity of the coating composition at this time is usually in the range of 100 to 5000 cps, preferably 500 to 2500 cps at 25 ° C.

The coating composition thus prepared is applied to one surface of the substrate film, and the organic solvent contained in the coating layer is removed.
Thus, the polyisocyanate compound (D) contained in the coating layer is coated on the surface of the substrate and the coating layer from which the organic solvent has been removed is aged under humid conditions to absorb moisture into the coating layer. And water are reacted to form a multimer of the polyisocyanate compound (D). This polyisocyanate compound (D) reacts with moisture in the air during aging to proceed the multimerization reaction of the polyisocyanate compound (D), but this polyisocyanate compound (D) has a low Tg (
It hardly reacts with the (meth) acrylate polymer (A) or the high Tg (meth) acrylate polymer (B). It is considered that the low Tg (meth) acrylate polymer (A) is constrained by the multimerized polyisocyanate compound formed at the portion where the low Tg (meth) acrylate polymer (A) molecule is entangled. Furthermore, an intramolecular cross-linked structure is formed mainly in the molecule of the high Tg (meth) acrylate polymer (B), and an intermolecular cross-linked structure is hardly formed. Accordingly, when the gel fraction of the component forming the adhesive layer of the optical member of the present invention is measured, it is less than 30% by weight, preferably 10% by weight or less, and more preferably substantially 0% by weight. When the pressure-sensitive adhesive that forms the pressure-sensitive adhesive layer after aging is analyzed by gel permeation chromatography (GPC), a peak of a compound having a molecular weight approximately several times the molecular weight of the polyisocyanate compound (D) used is observed. Isocyanate compound (D) is polymerized by absorbing moisture in the air, and polyisocyanate compound (D) and low Tg (meth) acrylate polymer (A) or high Tg (meth) acrylate polymer (B) It can be confirmed that there is no direct reaction.

  On the other hand, the curing agent (C) contained in the composition reacts with the functional group in the high Tg (meth) acrylate polymer (B), but this curing agent (C) is mainly composed of high Tg (meta). ) The functional groups in the molecule of the acrylate polymer (B) are cross-linked with each other to form an intramolecular cross-linked structure. In this way, the flowability of the low Tg (meth) acrylate polymer (A) is controlled by forming a crosslinked structure in the molecule of the high Tg (meth) acrylate polymer (B) by the curing agent (C). The adhesive layer provided on the optical member of the present invention has a high holding power, and even if the stress is applied for a long time, the attached optical member does not shift its sticking position. As described above, a cross-linking structure is formed in the high Tg (meth) acrylate polymer by the curing agent (C), but this cross-linking structure hardly causes an intramolecular cross-linking structure or a gel fraction (three-dimensional). Since it has a crosslinked structure, the gel fraction of the pressure-sensitive adhesive forming the pressure-sensitive adhesive layer is less than 30% by weight, preferably 10% by weight or less, more preferably substantially 0% by weight. The molecular weight of the component forming the pressure-sensitive adhesive does not increase significantly.

  After applying the coating composition to the substrate surface, the polyisocyanate compound (D) and the curing agent (C) as described above are used in an environment having humidity, specifically, 10 to 100% humidity, preferably The reaction is carried out by aging under conditions of 60 to 95%, temperature of 10 to 80 ° C., preferably 20 to 50 ° C., for 24 hours to 14 days, preferably 3 days to 10 days. By aging in an environment having such humidity, the polyisocyanate compound (D) and the curing agent (C) react gently, and the gel fraction is less than 30% by weight, preferably substantially 0% by weight. An agent layer can be formed.

  In addition, as a base film which forms the optical member of this invention, the base film conventionally used like a polarizing plate or a phase difference plate can be used. In particular, when a polarizing plate having a large heat shrinkage is used, the effect of the optical member of the present invention is remarkable.

  The pressure-sensitive adhesive layer formed in this way has the fluidity of the low Tg (meth) acrylate polymer (A) by the high Tg (meth) acrylate polymer (B) having an intramolecular cross-linked structure formed by the curing agent (C). The polyisocyanate compound (D) absorbs moisture in the air and multimerizes, thereby causing molecular misalignment in the entangled portion of the molecule of the low Tg (meth) acrylate polymer (A). It is possible to improve the durability of the pressure-sensitive adhesive layer at high temperatures and the durability under high temperature and high humidity conditions.

In addition, since there is almost no three-dimensional cross-linking structure formed between the molecules, the optical member of the present invention hardly leaks light and can be used for a large screen display exceeding 20 inches, for example.
〔Example〕
Next, although an example is shown and explained about an optical member and its manufacturing method of the present invention, the present invention is not limited by these.
[Production Example 1]
<Production of low Tg (meth) acrylate polymer (A-1)>
n-Butyl acrylate (n-BA): 100 parts by weight, ethyl acetate: 100 parts by weight, azobisisobutyronitrile (AIBN): 0.2 parts by weight are put in a reaction vessel, and the air in the reaction vessel is nitrogen. After substituting with gas, this container was heated to 60 ° C. in a nitrogen atmosphere with stirring, and reacted for 6 hours.

After 6 hours, the reaction solution was diluted with a large excess of ethyl acetate to obtain a low Tg (meth) acrylate polymer (A-1). When the molecular weight of this low Tg (meth) acrylate polymer (A-1) was measured by gas permeation chromatography (GPC), the weight average molecular weight was 150.
It was ten thousand. In addition, the glass transition temperature (Tg) of this low Tg (meth) acrylate polymer (A-1)
) Was -54 ° C.
[Production Example 2]
<Production of low Tg (meth) acrylate polymer (A-2)>
n-butyl acrylate (n-BA): 99.9 parts by weight, acrylic acid (AA): 0.1 parts by weight, ethyl acetate: 100 parts by weight, azobisisobutyronitrile (AIBN): 0.2 parts by weight Was placed in a reaction vessel, and the air in the reaction vessel was replaced with nitrogen gas, and then the vessel was heated to 60 ° C. in a nitrogen atmosphere with stirring to carry out the reaction for 6 hours.

After 6 hours, the reaction solution was diluted with a large excess of ethyl acetate to obtain a low Tg (meth) acrylate polymer (A-2). When the molecular weight of this low Tg (meth) acrylate polymer (A-2) was measured by GPC in the same manner as in Production Example 1, the weight average molecular weight was 1,500,000. Moreover, the glass transition temperature (Tg) of this low Tg (meth) acrylate polymer (A-2) was -53.9 degreeC.
[Production Example 3]
<Production of low Tg (meth) acrylate polymer (A-3)>
n-butyl acrylate (n-BA): 99.7 parts by weight, acrylic acid (AA): 0.3 parts by weight, ethyl acetate: 100 parts by weight, azobisisobutyronitrile (AIBN): 0.2 parts by weight Was placed in a reaction vessel, and the air in the reaction vessel was replaced with nitrogen gas, and then the vessel was heated to 60 ° C. in a nitrogen atmosphere with stirring to carry out the reaction for 6 hours.

After 6 hours, the reaction solution was diluted with a large excess of ethyl acetate to obtain a low Tg (meth) acrylate polymer (A-3). When the molecular weight of this low Tg (meth) acrylate polymer (A-3) was measured by GPC in the same manner as in Production Example 1, the weight average molecular weight was 1,600,000. Moreover, the glass transition temperature (Tg) of this low Tg (meth) acrylate polymer (A-3) was -53.7 degreeC.
[Production Example 4]
<Production of low Tg (meth) acrylate polymer (A-4)>
n-butyl acrylate (n-BA): 99.9 parts by weight, acrylic acid (AA): 0.1 parts by weight, ethyl acetate: 100 parts by weight, toluene: 20 parts by weight, azobisisobutyronitrile (AIBN) : 0.2 part by weight was put into a reaction vessel, and the air in the reaction vessel was replaced with nitrogen gas, and then the vessel was heated to 70 ° C. in a nitrogen atmosphere with stirring, and the reaction was performed for 6 hours. went.

After 6 hours, the reaction solution was diluted with a large excess of ethyl acetate to obtain a low Tg (meth) acrylate polymer (A-4). When the molecular weight of this low Tg (meth) acrylate polymer (A-4) was measured by GPC in the same manner as in Production Example 1, the weight average molecular weight was 700,000. Moreover, the glass transition temperature (Tg) of this low Tg (meth) acrylate polymer (A-4) was -53.9 degreeC.
[Production Example 5]
<Production of low Tg (meth) acrylate polymer (A-5)>
n-butyl acrylate (n-BA): 95 parts by weight, acrylic acid (AA): 5 parts by weight, ethyl acetate: 100 parts by weight, azobisisobutyronitrile (AIBN): 0.2 parts by weight in a reaction vessel Then, after the air in the reaction vessel was replaced with nitrogen gas, the vessel was heated to 60 ° C. in a nitrogen atmosphere under stirring and reacted for 6 hours.

After 6 hours, the reaction solution was diluted with a large excess of ethyl acetate to obtain a low Tg (meth) acrylate polymer (A-5). When the molecular weight of this low Tg (meth) acrylate polymer (A-5) was measured by GPC in the same manner as in Production Example 1, the weight average molecular weight was 1,500,000. Moreover, the glass transition temperature (Tg) of this low Tg (meth) acrylate polymer (A-5) was -49.3 degreeC.
[Production Example 6]
<Production of low Tg (meth) acrylate polymer (A-6)>
Ethyl acrylate (EA): 65 parts by weight, n-butyl acrylate (BA) 30 parts by weight Acrylic acid (AA): 5 parts by weight, ethyl acetate: 120 parts by weight, azobisisobutyronitrile (AIBN): 0.2 Part by weight was placed in a reaction vessel, and the air in the reaction vessel was replaced with nitrogen gas, and then the vessel was heated to 60 ° C. in a nitrogen atmosphere with stirring, and reacted for 6 hours.

After 6 hours, the reaction solution was diluted with a large excess of ethyl acetate to obtain a low Tg (meth) acrylate polymer (A-6). When the molecular weight of this low Tg (meth) acrylate polymer (A-6) was measured by GPC in the same manner as in Production Example 1, the weight average molecular weight was 1,500,000. Moreover, the glass transition temperature (Tg) of this low Tg (meth) acrylate polymer (A-6) was -29.8 degreeC.
[Production Example 7]
<Production of high Tg (meth) acrylate polymer (B-1)>
tert-butyl acrylate (t-BA): 90 parts by weight, acrylic acid (AA): 10 parts by weight, ethyl acetate: 100 parts by weight, azobisisobutyronitrile (AIBN): 0.2 parts by weight in a reaction vessel Then, after the air in the reaction vessel was replaced with nitrogen gas, the vessel was heated to 60 ° C. in a nitrogen atmosphere under stirring and reacted for 6 hours.

After 6 hours, the reaction solution was diluted with a large excess of ethyl acetate to obtain a high Tg (meth) acrylate polymer (B-1). When the molecular weight of this high Tg (meth) acrylate polymer (B-1) was measured by GPC in the same manner as in Production Example 1, the weight average molecular weight was 1,200,000. Moreover, the glass transition temperature (Tg) of this high Tg (meth) acrylate polymer (B-1) was 46.5 degreeC.
[Production Example 8]
<Production of high Tg (meth) acrylate polymer (B-2)>
Tert-butyl acrylate (t-BA): 80 parts by weight, acrylic acid (AA): 20 parts by weight, ethyl acetate: 100 parts by weight, azobisisobutyronitrile (AIBN): 0.2 parts by weight in a reaction vessel Then, after the air in the reaction vessel was replaced with nitrogen gas, the vessel was heated to 60 ° C. in a nitrogen atmosphere under stirring and reacted for 6 hours.

After 6 hours, the reaction solution was diluted with a large excess of ethyl acetate to obtain a high Tg (meth) acrylate polymer (B-2). When the molecular weight of this high Tg (meth) acrylate polymer (B-2) was measured by GPC in the same manner as in Production Example 1, the weight average molecular weight was 1,050,000. Moreover, the glass transition temperature (Tg) of this high Tg (meth) acrylate polymer (B-2) was 52 degreeC.
[Production Example 9]
<Production of high Tg (meth) acrylate polymer (B-3)>
n-butyl methacrylate (n-BMA): 94 parts by weight, acrylic acid (AA): 6 parts by weight, ethyl acetate: 100 parts by weight, azobisisobutyronitrile (AIBN): 0.2 parts by weight in a reaction vessel Then, after the air in the reaction vessel was replaced with nitrogen gas, the vessel was heated to 70 ° C. in a nitrogen atmosphere under stirring and reacted for 6 hours.

After 6 hours, the reaction solution was diluted with a large excess of ethyl acetate to obtain a high Tg (meth) acrylate polymer (B-3). When the molecular weight of this high Tg (meth) acrylate polymer (B-3) was measured by GPC in the same manner as in Production Example 1, the weight average molecular weight was 800,000. Moreover, the glass transition temperature (Tg) of this high Tg (meth) acrylate polymer (B-3) was 24.0 degreeC.
[Production Example 10]
<Production of high Tg (meth) acrylate polymer (B-4)>
tert-butyl acrylate (t-BA): 90 parts by weight, acrylic acid (AA): 10 parts by weight, ethyl acetate: 35 parts by weight, toluene: 75 parts by weight, azobisisobutyronitrile (AIBN): 0.2 Part by weight was placed in a reaction vessel, and the air in the reaction vessel was replaced with nitrogen gas, and then the vessel was heated to 70 ° C. in a nitrogen atmosphere with stirring and reacted for 6 hours.

After 6 hours, the reaction solution was diluted with a large excess of ethyl acetate to obtain a high Tg (meth) acrylate polymer (B-4). When the molecular weight of this high Tg (meth) acrylate polymer (B-4) was measured by GPC in the same manner as in Production Example 1, the weight average molecular weight was 400,000. Moreover, the glass transition temperature (Tg) of this high Tg (meth) acrylate polymer (B-4) was 46.5 degreeC.
[Production Example 11]
<Production of high Tg (meth) acrylate polymer (B-5)>
tert-butyl acrylate (t-BA): 95 parts by weight, acrylic acid (AA): 5 parts by weight, ethyl acetate: 100 parts by weight, azobisisobutyronitrile (AIBN): 0.2 parts by weight in a reaction vessel Then, after the air in the reaction vessel was replaced with nitrogen gas, the vessel was heated to 60 ° C. in a nitrogen atmosphere under stirring and reacted for 6 hours.

After 6 hours, the reaction solution was diluted with a large excess of ethyl acetate to obtain a high Tg (meth) acrylate polymer (B-5). When the molecular weight of this high Tg (meth) acrylate polymer (B-5) was measured by GPC in the same manner as in Production Example 1, the weight average molecular weight was 1,200,000. Moreover, the glass transition temperature (Tg) of this high Tg (meth) acrylate polymer (B-5) was 43.7 degreeC.
[Production Example 12]
<Production of high Tg (meth) acrylate polymer (B-6)>
Iso-butyl acrylate (i-BA): 90 parts by weight, acrylic acid (AA): 10 parts by weight, ethyl acetate: 100 parts by weight, azobisisobutyronitrile (AIBN): 0.2 parts by weight in a reaction vessel Then, after the air in the reaction vessel was replaced with nitrogen gas, the vessel was heated to 60 ° C. in a nitrogen atmosphere under stirring and reacted for 6 hours.

After 6 hours, the reaction solution was diluted with a large excess of ethyl acetate to obtain a high Tg (meth) acrylate polymer (B-6). When the molecular weight of this high Tg (meth) acrylate polymer (B-6) was measured by GPC in the same manner as in Production Example 1, the weight average molecular weight was 1,200,000. Moreover, the glass transition temperature (Tg) of this high Tg (meth) acrylate polymer (B-6) was -15.2 degreeC.
[Production Example 13]
<Production of (meth) acrylate polymer (B-7)>
n-butyl acrylate (n-BA): 90 parts by weight, acrylic acid (AA): 4.8 parts by weight, 2-hydroxyethyl acrylate (2HEA): 0.2 parts by weight, styrene macromonomer (AS-6; Toa Synthetic Co., Ltd.): 5 parts by weight, ethyl acetate: 100 parts by weight, azobisisobutyronitrile (AIBN): 0.2 parts by weight are placed in a reaction vessel, and the air in the reaction vessel is replaced with nitrogen gas. Then, the temperature of the container was raised to 60 ° C. in a nitrogen atmosphere under stirring, and the reaction was performed for 6 hours.

  After 6 hours, the reaction solution was diluted with a large excess of ethyl acetate to obtain a (meth) acrylate polymer (B-7). When the molecular weight of this (meth) acrylate polymer (B-7) was measured by GPC in the same manner as in Production Example 1, the weight average molecular weight was 1.1 million. Moreover, the glass transition temperature (Tg) of this (meth) acrylate polymer (B-7) was -44.6 degreeC.

The low Tg (meth) acrylate polymer (A-1) produced in Production Example 1 was 100 parts by weight in solid content, and the high Tg (meth) acrylate polymer (B-8) produced in Production Example 7 was 6 in solid content. Parts by weight, 0.03 parts by weight of an epoxy curing agent (E-5XM, manufactured by Soken Chemical Co., Ltd.), 2 parts by weight of an isocyanate curing agent (L-45, manufactured by Soken Chemical Co., Ltd.), and a silane cup 0.2 parts by weight of a ring agent (A-50, manufactured by Soken Chemical Co., Ltd.) was mixed. The obtained mixture (viscosity at 25 ° C .: 1000 cps) was applied to a release-treated polyester film and dried to form an adhesive layer having a thickness of 25 μm. The pressure-sensitive adhesive layer thus obtained was transferred to one side of a polarizing film and aged for 7 days under conditions of a temperature of 23 ° C. and a humidity of 65% to produce a polarizing film with a pressure-sensitive adhesive layer.

After 7 days, a part of the pressure-sensitive adhesive layer was taken and its gel fraction was measured. The gel fraction was 0% by weight, and this pressure-sensitive adhesive layer had molecules that were measured as gel fractions. No intercrosslinking structure is formed. The pressure-sensitive adhesive forming this pressure-sensitive adhesive layer was analyzed using GPC.
As shown in FIG. 1, in addition to the peak A (weight average molecular weight = about 1,200,000) corresponding to the polymer substance forming the pressure-sensitive adhesive layer, a peak (peak B) is detected around the weight average molecular weight of about 1400. The peak B is presumed to be a polyisocyanate compound multimer (approximately equivalent to a dimer) from its molecular weight.

The obtained polarizing film with an adhesive layer was examined for light leakage at 85 ° C., durability at 85 ° C., and durability at 65 ° C. × 85%. The reworkability of this polarizing film with a pressure-sensitive adhesive layer was also examined. The results are shown in Table 1. The light leakage, the durability at 85 ° C., the durability at 60 ° C. × 95%, the reworkability measuring method and evaluation criteria in Table 1 are as follows.
Light leakage at 85 ° C. Measurement method Two obtained polarizing films with adhesive layer (140 mm × 240 mm) are placed on the front and back surfaces of an alkali-free glass plate (trade name: 1737, manufactured by Corning). A test piece was prepared by adhering using a laminator roll so as to be in a crossed Nicols position, and then holding in an autoclave adjusted to 50 ° C. and 5 atm for 20 minutes.

The prepared test piece was allowed to stand at 85 ° C. for 500 hours, and light leakage was visually observed and evaluated.
Evaluation criteria: No light leakage is observed.
X: Light leakage is clearly observed.
Durability (85 ℃, 65 ℃ × 95% RH)
Measurement method The obtained polarizing film with a pressure-sensitive adhesive layer (140 mm × 240 mm) is attached to one side of a non-alkali glass plate using a laminator roll, and then held in an autoclave adjusted to 50 ° C. and 5 atm for 20 minutes. A test piece was prepared.

Two test pieces were prepared from each of the pressure-sensitive adhesive compositions, and allowed to stand for 500 hours under conditions of 85 ° C. or 65 ° C. × RH 96%, and the occurrence of foaming, peeling and cracking was visually observed and evaluated.
Evaluation criteria: No appearance defects such as foaming, peeling and cracking.
X: Foaming, peeling, cracks, etc. are observed.
Reworkability Measuring method The obtained polarizing film with an adhesive layer (140 mm x 240 mm) was attached to one side of an alkali-free glass plate using a laminator roll, and then adjusted to 50C and 5 atm. A test piece was prepared by holding in an autoclave for 20 minutes.

The optical film was peeled off from the test piece thus prepared, and the contamination and peelability of the adherend were confirmed.
Evaluation criteria
Contamination ○: The adherend was not contaminated.

X: Contamination was confirmed on the adherend.
Peel strength ○: Peeled easily by hand.

    X: Peeling was heavy and did not peel easily.

In Example 1, instead of the low Tg (meth) acrylate polymer (A-1), the low Tg (meth) acrylate polymer (A-2) produced in Production Example 2 was used, and the high Tg (meth) acrylate polymer was used. High Tg (meth) acrylate polymer (B-1) produced in Production Example 7 instead of (B-8)
A polarizing film with an adhesive layer was produced in the same manner except that was used.

After 7 days, a part of the pressure-sensitive adhesive layer was taken and its gel fraction was measured. The gel fraction was 0% by weight, and this pressure-sensitive adhesive layer had molecules that were measured as gel fractions. No intercrosslinking structure is formed. The pressure-sensitive adhesive forming this pressure-sensitive adhesive layer was analyzed using GPC.
A peak considered to be a multimer of a polyisocyanate compound having absorbed water was observed in the vicinity of a molecular weight of 1400.

  About the obtained polarizing film with an adhesive layer, the characteristic was investigated like Example 1. FIG. The results are shown in Table 1.

In Example 1, instead of the low Tg (meth) acrylate polymer (A-1), the low Tg (meth) acrylate polymer (A-3) produced in Production Example 3 was used, and the high Tg (meth) acrylate polymer was used. (B-8): A polarizing film with an adhesive layer was prepared in the same manner except that 8 parts by weight of the high Tg (meth) acrylate polymer (B-1) produced in Production Example 7 was used instead of 6 parts by weight. Manufactured.

After 7 days, a part of the pressure-sensitive adhesive layer was taken and its gel fraction was measured. The gel fraction was 0% by weight, and this pressure-sensitive adhesive layer had molecules that were measured as gel fractions. No intercrosslinking structure is formed. The pressure-sensitive adhesive forming this pressure-sensitive adhesive layer was analyzed using GPC.
A peak considered to be a multimer of a polyisocyanate compound having absorbed water was observed in the vicinity of a molecular weight of 1400.

  About the obtained polarizing film with an adhesive layer, the characteristic was investigated like Example 1. FIG. The results are shown in Table 1.

In Example 1, instead of the low Tg (meth) acrylate polymer (A-1), the low Tg (meth) acrylate polymer (A-2) produced in Production Example 2 was used, and the high Tg (meth) acrylate polymer was used. (B-8): A polarizing film with an adhesive layer was prepared in the same manner except that 2 parts by weight of the high Tg (meth) acrylate polymer (B-1) produced in Production Example 8 was used instead of 6 parts by weight. Manufactured.

After 7 days, a part of the pressure-sensitive adhesive layer was taken and its gel fraction was measured. The gel fraction was 0% by weight, and this pressure-sensitive adhesive layer had molecules that were measured as gel fractions. No intercrosslinking structure is formed. The pressure-sensitive adhesive forming this pressure-sensitive adhesive layer was analyzed using GPC.
A peak considered to be a multimer of a polyisocyanate compound having absorbed water was observed in the vicinity of a molecular weight of 1400.

  About the obtained polarizing film with an adhesive layer, the characteristic was investigated like Example 1. FIG. The results are shown in Table 1.

In Example 1, instead of the low Tg (meth) acrylate polymer (A-1), the low Tg (meth) acrylate polymer (A-3) produced in Production Example 3 was used, and the high Tg (meth) acrylate polymer was used. (B-8): Instead of 6 parts by weight, the glass transition temperature (Tg) produced in Production Example 9 = 24.0 ° C. High Tg (meth) acrylate polymer (B-3): except that 4 parts by weight were used Similarly, a polarizing film with a pressure-sensitive adhesive layer was produced.

After 7 days, a part of the pressure-sensitive adhesive layer was taken and its gel fraction was measured. The gel fraction was 0% by weight, and this pressure-sensitive adhesive layer had molecules that were measured as gel fractions. No intercrosslinking structure is formed. The pressure-sensitive adhesive forming this pressure-sensitive adhesive layer was analyzed using GPC.
A peak considered to be a multimer of a polyisocyanate compound having absorbed water was observed in the vicinity of a molecular weight of 1700.

About the obtained polarizing film with an adhesive layer, the characteristic was investigated like Example 1. FIG. The results are shown in Table 1.
[Comparative Example 1]
In Example 1, instead of the low Tg (meth) acrylate polymer (A-1), the low Tg (meth) acrylate polymer (A-4) having a weight average molecular weight of 700,000 produced in Production Example 4 was used.
A polarizing film with an adhesive layer was produced in the same manner except that the high Tg (meth) acrylate polymer (B-1) produced in Production Example 7 was used instead of the high Tg (meth) acrylate polymer (B-8). did.

About the obtained polarizing film with an adhesive layer, the characteristic was investigated like Example 1. FIG. The results are shown in Table 1.
[Comparative Example 2]
In Example 1, instead of the low Tg (meth) acrylate polymer (A-1), the low Tg (meth) acrylate polymer (A-2) produced in Production Example 2 was used, and the high Tg (meth) acrylate polymer was used. A polarizing film with an adhesive layer was produced in the same manner except that the high Tg (meth) acrylate polymer (B-4) having a weight average molecular weight of 400,000 produced in Production Example 10 was used instead of (B-8). .

About the obtained polarizing film with an adhesive layer, the characteristic was investigated like Example 1. FIG. The results are shown in Table 1.
[Comparative Example 3]
In Example 1, instead of the low Tg (meth) acrylate polymer (A-1), the low Tg (meth) acrylate polymer (A-2) produced in Production Example 2 was used, and the high Tg (meth) acrylate polymer was used. (B-8): Instead of the hexagonal dragon part, the high Tg (meth) acrylate polymer produced in Production Example 7 (B-1): With the same adhesive layer except that 0.5 part by weight was used A polarizing film was produced.

About the obtained polarizing film with an adhesive layer, the characteristic was investigated like Example 1. FIG. The results are shown in Table 1.
[Comparative Example 4]
In Example 1, instead of the low Tg (meth) acrylate polymer (A-1), the low Tg (meth) acrylate polymer (A-2) produced in Production Example 2 was used, and the high Tg (meth) acrylate polymer was used. (B-8): A polarizing film with a pressure-sensitive adhesive layer was prepared in the same manner except that 40 parts by weight of the high Tg (meth) acrylate polymer (B-1) produced in Production Example 7 was used instead of 6 parts by weight. Manufactured. The gel fraction of the pressure-sensitive adhesive layer forming component of the produced polarizing film with a pressure-sensitive adhesive layer was 50% by weight, and an intermolecular cross-linked structure was formed in the pressure-sensitive adhesive forming component.

About the obtained polarizing film with an adhesive layer, the characteristic was investigated like Example 1. FIG. The results are shown in Table 1.
[Comparative Example 5]
In Example 1, instead of the low Tg (meth) acrylate polymer (A-1), the copolymerization of the functional group-containing monomer produced in Production Example 5 was 5% by weight of the low Tg (meth) acrylate polymer (A-5). ), And instead of the high Tg (meth) acrylate polymer (B-8), the adhesive layer was similarly used except that the high Tg (meth) acrylate polymer (B-1) produced in Production Example 7 was used. An attached polarizing film was produced. The gel fraction of the pressure-sensitive adhesive layer forming component of the produced polarizing film with a pressure-sensitive adhesive layer was 60% by weight, and an intermolecular cross-linked structure was formed in the pressure-sensitive adhesive forming component.

About the obtained polarizing film with an adhesive layer, the characteristic was investigated like Example 1. FIG. The results are shown in Table 1.
[Comparative Example 6]
In Example 1, instead of the low Tg (meth) acrylate polymer (A-1), the low Tg (meth) acrylate polymer (A-2) produced in Production Example 2 was used, and the high Tg (meth) acrylate polymer was used. In place of (B-8), the same procedure was performed except that a high Tg (meth) acrylate polymer (B-5) in which the copolymerization amount of the functional group-containing monomer produced in Production Example 11 was 5% by weight was used. A polarizing film with an agent layer was produced.

About the obtained polarizing film with an adhesive layer, the characteristic was investigated like Example 1. FIG. The results are shown in Table 1.
[Comparative Example 7]
In Example 1, instead of the low Tg (meth) acrylate polymer (A-1), the low Tg (meth) acrylate polymer (A-2) produced in Production Example 2 was used, and the high Tg (meth) acrylate polymer was used. Instead of (B-8), the glass transition temperature (Tg) produced in Production Example 12 was −15.2 ° C.
A polarizing film with an adhesive layer was produced in the same manner except that the high Tg (meth) acrylate polymer (B-6) was used.

About the obtained polarizing film with an adhesive layer, the characteristic was investigated like Example 1. FIG. The results are shown in Table 1.
[Comparative Example 8]
In Example 1, instead of the low Tg (meth) acrylate polymer (A-1), a low Tg (meth) acrylate polymer (A) having a glass transition temperature (Tg) of −23.9 ° C. produced in Production Example 6 was used. -2), and in the same manner except that the high Tg (meth) acrylate polymer (B-1) produced in Production Example 7 was used instead of the high Tg (meth) acrylate polymer (B-8). A polarizing film with an agent layer was produced.

About the obtained polarizing film with an adhesive layer, the characteristic was investigated like Example 1. FIG. The results are shown in Table 1.
[Comparative Example 9]
In Example 1, instead of the low Tg (meth) acrylate polymer (A-1), Production Example 13
N-Butyl acrylate (n-BA) prepared in the above: 90 parts by weight, acrylic acid (AA): 4.8 parts by weight, 2-hydroxyethyl acrylate (2HEA): 0.2 parts by weight, styrene macromonomer (AS
-6, manufactured by Toagosei Co., Ltd.): copolymer with 5 parts by weight (weight average molecular weight: 1.1 million, glass transition temperature (Tg) = -44.6 ° C, high Tg (meth) acrylate polymer In the same manner as in Example 1 except that 1.2 parts by weight of L-45, which is a commercially available polyisocyanate compound, was used as the polyisocyanate compound, and no epoxy curing agent and silane coupling agent were used. Thus, the pressure-sensitive adhesive layer-forming component has a gel fraction of 50% by weight, and the pressure-sensitive adhesive-forming component has an intermolecular cross-linked structure. It was.

  As a result of GPC measurement, no peak of molecular weight due to multimerization of L-45 was observed, but as a result of instrumental analysis, the peak due to the isocyanate group disappeared, and the isocyanate was intermolecularly crosslinked. It was suggested to be involved in the formation of the structure.

About the obtained polarizing film with an adhesive layer, the characteristic was investigated like Example 1. FIG. The results are shown in Table 1.
[Comparative Example 10]
In Example 1, the high Tg (meth) acrylate polymer (B-1) produced in Production Example 7 was used instead of the high Tg (meth) acrylate polymer (B-8), and no polyisocyanate compound was used. A polarizing film with an adhesive layer was produced in the same manner except that. In the production of the polarizing film with the pressure-sensitive adhesive layer, aging was carried out in a dry atmosphere, and therefore no GPC peak having a molecular weight that was attributed to an increase in the amount of polyisocyanate compound was observed.

About the obtained polarizing film with an adhesive layer, the characteristic was investigated like Example 1. FIG. The results are shown in Table 1.
[Comparative Example 11]
In Example 1, except that the low Tg (meth) acrylate polymer (A-1) and the high Tg (meth) acrylate polymer (B-8) were used and the aging conditions were aged in a dry atmosphere at 40 ° C. for 7 days. Produced a polarizing film with an adhesive layer in the same manner.

About the obtained polarizing film with an adhesive layer, the characteristic was investigated like Example 1. FIG. The results are shown in Table 1.
[Comparative Example 12]
In Example 1, a polarizing film with an adhesive layer was produced in the same manner except that E-5XM as a curing agent was not used.

About the obtained polarizing film with an adhesive layer, the characteristic was investigated like Example 1. FIG. The results are shown in Table 1.
[Comparative Example 13]
A polarizing film with a pressure-sensitive adhesive layer was produced in the same manner as in Example 2 except that the high Tg (meth) acrylate polymer (B) was not used.

  About the obtained polarizing film with an adhesive layer, the characteristic was investigated like Example 1. FIG. The results are shown in Table 1.

As is clear from the comparison between Example 2 and Comparative Example 6 shown in Table 1 (3) above, Example 2 and Comparative Example 6 are both low Tg (meth) acrylate polymers (A) in Production Example 2. In Example 2, 99.9 parts by weight of n-butyl acrylate and 0.1 part by weight of acrylic acid were copolymerized with a weight average molecular weight of 1.5 million and a glass transition temperature of −53.9 ° C. 9. 90.0 parts by weight of tert-butyl acrylate and 10% acrylic acid as high Tg (meth) acrylate polymer (B)
While a copolymer having a weight average molecular weight of 1,200,000 copolymerized with 0 part by weight and a glass transition temperature of 46.5 ° C. is used, in Comparative Example 6, 95.0 parts by weight of tert-butyl acrylate and acrylic acid are used. A copolymer having a weight average molecular weight of 1,200,000 and a glass transition temperature of 43.7 ° C. copolymerized by 5.0 parts by weight is used. In Example 2 and Comparative Example 6, the type and amount of the curing agent, the amount and amount of polyisocyanate compound (D) used, and the aging conditions were the same, and each adhesive had a gel fraction of 0% by weight. The intermolecular cross-linked structure is not formed, or it is considered that the molecular weight is not so high as to be gelled.

  When a high Tg (meth) acrylate polymer (B) having a small copolymerization amount of acrylic acid as shown in Comparative Example 6 is used, the intramolecular cross-linking structure is not sufficiently formed, and the pressure-sensitive adhesive flows. The holding power of the layer is reduced.

Further, when Example 1 (humidity 65%) and Comparative Example 11 (humidity 0%) having different aging conditions are compared, in Comparative Example 11, multimerization of the polyisocyanate compound (D) proceeds due to moisture absorption. Therefore, it is not restrained by the polyisocyanate compound (D) in which the low Tg (meth) acrylate polymer (A) is multimerized, and the holding power is poor. On the other hand, in Example 1, the polyisocyanate compound absorbs moisture and multimerizes, so that the movement of the low Tg (meth) acrylate polymer (A) is caused by the multimerized polyisocyanate compound (D). As a result, the holding force is increased. The carboxyl group in the high Tg (meth) acrylate polymer (B) and the polyisocyanate compound (D) are low in reactivity, and the gel fraction of the forming component of the formed pressure-sensitive adhesive layer is 0% by weight. Further, when the formation component of the formed pressure-sensitive adhesive layer is analyzed using gel permeation chromatography (GPC), a peak is observed at a position of a molecular weight of about 1400, and this peak corresponds to the polyisocyanate compound (D) used. Since it corresponds to the molecular weight of the dimer, no cross-linked structure is formed by the polyisocyanate compound (D).

  Further, when Comparative Example 12 that does not use the epoxy compound that is the curing agent (C) is compared with Example 1, Comparative Example 11 does not use the epoxy compound that is the curing agent, so the gel fraction is the same as that of Example 1. Similarly, although the content is 0% by weight, since the intramolecular cross-linked structure is not formed, the durability under high temperature and high humidity conditions is poor. Further, in Comparative Example 13 in which the high Tg (meth) acrylate polymer (B) is not used, durability is not sufficiently exhibited because an intramolecular crosslinked structure is not formed.

  From the above results, the pressure-sensitive adhesive layer formed on the optical member of the present invention has almost no three-dimensional cross-linked structure formed by intermolecular cross-linking so as to generate a gel fraction. The compound (D) is considered to exhibit durability by restraining the movement of the low Tg (meth) acrylate polymer (A) by absorbing water in the air and polymerizing it during aging. . And since the gel fraction of the component which forms the adhesive layer of the optical member of this invention is substantially 0 weight%, light leakage does not arise.

  The optical member of the present invention has sufficient strength despite the low gel fraction, and also has the property that light leakage hardly occurs from the pressure-sensitive adhesive layer of the optical member of the present invention. Therefore, the optical member of the present invention can be used as a polarizing plate or a retardation plate used in a large screen display.

  In particular, in the present invention, a polyisocyanate compound (D) is contained in the composition, and such polyisocyanate compound (D) undergoes a multimerization reaction selectively in the presence of moisture, The reaction of the polyisocyanate compound (D) with moisture absorbs moisture in the air and the like in a large amount when the content of the group having high reactivity with the polyisocyanate compound (D) is low. The reaction for forming a body proceeds selectively and hardly contributes to the reaction for forming an intermolecular cross-linked structure.

Further, in the low Tg acrylate polymer (A) blended in a relatively large amount in the pressure-sensitive adhesive layer forming the optical member of the present invention, since the copolymerization amount of the functional group-containing monomer is low, the curing agent (C) or It hardly binds to the polyisocyanate compound (D) to form an intermolecular cross-linked structure, and the high Tg (meth) acrylate polymer (B) is composed of the above-mentioned low Tg (meth) acrylate polymer (
The copolymerization amount of the functional group-containing monomer is higher than that of A), but the blending amount of the high Tg (meth) acrylate polymer (B) itself is small, and an effective intermolecular crosslinking structure can be formed with such a small amount. It is difficult to form an intramolecular cross-linked structure between adjacent functional groups in the same molecule, or a three-dimensional cross-linked structure is formed by intermolecular cross-linking that does not cause gel fraction. . Thus, even when a crosslinked structure is formed by the curing agent, the gel fraction hardly changes, but the high Tg (meth) acrylate polymer (B) thus formed has a molecular structure due to the crosslinked structure. The movement is restricted, and it is a deterrent to the movement of molecules even for the low Tg (meth) acrylate polymer (A). Furthermore, the polyisocyanate compound (D) that has absorbed and absorbed water in the aging step is formed in the entangled portion of the low Tg (meth) acrylate polymer (A), and the low Tg (meth) acrylate polymer (A ) Is controlled so that light leakage from the adhesive layer is small in the optical member of the present invention. Further, as described above, each component forming the pressure-sensitive adhesive has a relationship with each other and suppresses movement of other components, so that it is excellent in durability and light leakage resistance.

1 is a GPC chart measured for the pressure-sensitive adhesive layer of the optical member produced in Example 1. FIG.

Explanation of symbols

A: Peak with a weight average molecular weight of about 1.2 million
B: Peak with a weight average molecular weight of about 1400

Claims (14)

(A) The glass transition temperature is −60 ° C. to −30 ° C., the weight average molecular weight is 1.2 million to 2 million, and the copolymerization amount of the monomer containing a functional group capable of reacting with the curing agent is 0 to 0. A low Tg (meth) acrylic polymer that is 5% by weight ;
(B) The glass transition temperature is 20 ° C. to 80 ° C., the weight average molecular weight is 500,000 to 2,000,000 , and the copolymerization amount of the monomer containing a functional group capable of reacting with the curing agent is 6% by weight to 20%. High Tg (meth) acrylic polymer in weight percent ; 1-15 parts by weight;
(C) at least one curing agent selected from the group consisting of epoxy curing agents, amine curing agents and metal chelate compound curing agents; 0.003 to 0.5 parts by weight;
(D) a polyisocyanate compound; a composition containing 0.5 to 3 parts by weight,
An optical member, wherein a pressure-sensitive adhesive layer that is aged so as to have a gel fraction of less than 30% by weight in an environment having humidity is formed on a surface of a substrate.   The monomer containing a functional group capable of reacting with the crosslinking agent is selected from the group consisting of a carboxyl group-containing (meth) acrylic monomer, an amino group-containing (meth) acrylic monomer, and an amide group-containing (meth) acrylic monomer. 2. The optical member according to claim 1, wherein the optical member is at least one type of functional group-containing monomer. 2. The optical member according to claim 1, wherein the pressure-sensitive adhesive layer has a thickness in the range of 10 to 50 μm.   The environment having a humidity for aging the composition is a temperature of 10 to 80 ° C. and a humidity of 10 to 100%, and the coating layer made of the composition is aged for 24 hours to 14 days in the environment. 2. The optical member according to claim 1, wherein The copolymerization amount of the monomer containing a functional group capable of reacting with the curing agent in the (A) low Tg (meth) acrylic polymer is in the range of 0 to 0.3% by weight. Section 1
The optical member according to item.   2. The optical member according to claim 1, further comprising a silane coupling agent (E) in the composition. The optical member according to any one of claims 1 to 6 , wherein the optical member is a polarizing plate of a liquid crystal element. (A) The glass transition temperature is −60 ° C. to −30 ° C., the weight average molecular weight is 1.2 million to 2 million, and the copolymerization amount of the monomer containing a functional group capable of reacting with the curing agent is 0 to 0. A low Tg (meth) acrylic polymer that is 5% by weight ;
(B) The glass transition temperature is 20 ° C. to 80 ° C., the weight average molecular weight is 500,000 to 2,000,000 , and the copolymerization amount of the monomer containing a functional group capable of reacting with the curing agent is 6% by weight to 20%. High Tg (meth) acrylic polymer in weight percent ; 1-15 parts by weight;
(C) a curing agent selected from the group consisting of epoxy curing agents, amine curing agents and metal chelate compound curing agents; 0.003 to 0.5 parts by weight;
(D) a polyisocyanate compound; a composition containing 0.5 to 3 parts by weight,
A method for producing an optical member, wherein the composition is aged so that the gel fraction of the pressure-sensitive adhesive layer is less than 30% by weight in an environment having humidity. The monomer containing a functional group capable of reacting with the crosslinking agent is selected from the group consisting of a carboxyl group-containing (meth) acrylic monomer, an amino group-containing (meth) acrylic monomer, and an amide group-containing (meth) acrylic monomer. 9. The method for producing an optical member according to claim 8 , wherein the monomer is at least one functional group-containing monomer. The method for producing an optical member according to claim 8, wherein the pressure-sensitive adhesive layer in which the crosslinked structure is formed has a thickness in the range of 10 to 50 µm. The environment having a humidity for aging the composition is a temperature of 10 to 80 ° C. and a humidity of 10 to 100%, and the coating layer made of the composition is aged for 24 hours to 14 days in the environment. The method for producing an optical member according to claim 8 . The copolymerization amount of the monomer containing a functional group capable of reacting with the curing agent in the (A) low Tg (meth) acrylic polymer is in the range of 0 to 0.3% by weight. The manufacturing method of the optical member of claim | item 8 . The method for producing an optical member according to claim 8 , wherein the composition further contains a silane coupling agent (E). The method for producing an optical member according to any one of claims 8 to 13 , wherein the optical member is a polarizing plate of a liquid crystal element.