JP2016183351A - Adhesive composition and application thereof - Google Patents

Abstract

PROBLEM TO BE SOLVED: To provide an adhesive composition capable of exhibiting sufficient transparency and excellent adhesiveness to various adherends, especially glass, and an adhesive product using the same.SOLUTION: There is provided an adhesive composition containing a tackifier containing a vinyl polymer and an acrylic adhesive polymer, where the vinyl polymer contains a vinyl monomer having an amide group and/or an amino group in a range of over 10 mass% and 90 mass% or less in all constitutional units and having glass transition temperature (Tg) of 40 to 150°C and number average molecular weight of 500 to 10,000 and the acrylic adhesive polymer contains acrylic acid methoxyethyl as a constitutional monomer.SELECTED DRAWING: None

Description

  The present invention relates to a tackifier having a function of improving the adhesive strength by being blended with a pressure-sensitive adhesive, a pressure-sensitive adhesive composition containing the tackifier, and a pressure-sensitive adhesive product using the same.

The pressure-sensitive adhesive (also referred to as a pressure-sensitive adhesive) is processed into a form such as a tape or a label, and is used in a wide range of applications. Further, the adherend is also applied to various substances such as plastic, paper, metal, glass and ceramics.
On the other hand, due to the dramatic advancement of electronics technology in recent years, various flat panel displays (FPD) such as liquid crystal displays (LCD) and plasma display panels (PDP) have come to be used as display devices in various fields. It was.
These display devices generally have a laminated structure in which a transparent plastic material such as glass or polycarbonate is bonded with an adhesive. For this reason, pressure-sensitive adhesives are required to have sufficient adhesive strength for these materials and excellent transparency, and acrylic pressure-sensitive adhesives are generally used. Further improvement is desired in terms of adhesion and adhesion.

Various pressure-sensitive adhesive compositions have been proposed in response to the above requirements.
Patent Document 1 discloses a pressure-sensitive adhesive composition including an acrylic cross-linked polymer having an alkoxyalkyl acrylate as a main monomer, without a carboxyl group-containing monomer component, as a pressure-sensitive adhesive composition having excellent adhesiveness and transparency. ing. Patent Document 2 describes that an acrylic polymer compound containing a monomer containing an amide group as a constituent monomer is useful as a pressure-sensitive adhesive composition for a touch panel.

  A pressure-sensitive adhesive composition in which a tackifier is added to a pressure-sensitive adhesive base polymer is also widely known for the purpose of increasing the adhesive strength of the pressure-sensitive adhesive. As the tackifier, for example, rosin resin, terpene resin, petroleum resin, low molecular weight acrylic polymer, etc. are known, but tackifier made of rosin resin, terpene resin or petroleum resin. In some cases, the pressure-sensitive adhesive composition containing the dye causes problems such as coloring and discoloration. In order to prevent problems such as coloring, a hydrogenated resin or a hydrocarbon-based resin may be used, but the compatibility with the acrylic adhesive polymer as the adhesive base polymer is insufficient, Transparency may be impaired and adhesion may be reduced.

Low molecular weight acrylic polymers are excellent in terms of compatibility and transparency with acrylic adhesive polymers, and some low molecular weight acrylic polymers that have been used in the same manner as tackifiers have been used so far. It is shown.
For example, Patent Document 3 discloses a pressure-sensitive adhesive composition containing a main polymer having a carboxyl group and a low molecular acrylic polymer having an amino group. Patent Document 4 discloses a pressure-sensitive adhesive layer comprising a pressure-sensitive adhesive composition comprising a polymer having a highly hydrophilic alkoxyalkyl (meth) acrylate as a main component and a low molecular weight acrylic polymer having an amino group or an amide group. It is described that it is effective for ensuring transparency even under high temperature and high humidity.

JP 2009-79203 A JP 2012-41456 A JP-A-10-310754 JP 2002-327160 A

However, none of the pressure-sensitive adhesive compositions described in Patent Document 1 and Patent Document 2 has sufficient adhesive strength to various adherends such as glass and polycarbonate.
On the other hand, in the pressure-sensitive adhesive compositions described in Patent Document 3 and Patent Document 4, although the adhesive strength is improved, sufficient adhesive strength cannot be obtained depending on the adherend, for example, the adhesive strength to glass is low. Some things left room for improvement.

  An object of the present invention is to provide a tackifier that exhibits sufficient transparency and can exhibit excellent adhesion to various adherends, particularly glass, and a pressure-sensitive adhesive composition including the same, and further using the same. It is to provide an adhesive product.

  As a result of intensive studies in view of the above-mentioned problems, the present inventors are excellent in various adherends by using a pressure-sensitive adhesive composition containing a specific low molecular weight acrylic polymer having an amide group and / or an amino group as a constituent component. It was learned that it was possible to achieve both good adhesion and good transparency, and the present invention was completed.

The present invention is as follows.
[1] A pressure-sensitive adhesive composition containing a tackifier containing a vinyl polymer and an acrylic pressure-sensitive adhesive polymer,
The vinyl polymer contains a vinyl monomer having an amide group and / or an amino group in a range of more than 10% by mass and 90% by mass or less in all the structural units, and a glass transition temperature (Tg) of 40 to 40%. 150 ° C. and a number average molecular weight of 500 to 10,000,
The acrylic adhesive polymer contains methoxyethyl acrylate as a constituent monomer.
Adhesive composition.
[2] The pressure-sensitive adhesive composition according to [1], wherein the vinyl polymer excludes those containing cyclohexyl methacrylate as a constituent monomer.
[3] The vinyl monomer having an amide group and / or amino group is selected from the group consisting of (meth) acryloylmorpholine, (meth) acrylamide, dimethylaminomethyl (meth) acrylate and dimethylaminoethyl (meth) acrylate. The pressure-sensitive adhesive composition according to the above [1] or [2], wherein the pressure-sensitive adhesive composition is one or more selected vinyl monomers.
[4] The pressure-sensitive adhesive according to any one of [1] to [3], wherein 5 to 60 parts by weight of the tackifier is contained with respect to 100 parts by weight of the acrylic pressure-sensitive adhesive polymer. Composition.
[5] An adhesive processed article using the adhesive composition according to any one of [1] to [4].

  According to the pressure-sensitive adhesive composition containing the tackifier of the present invention, high adhesion strength can be obtained for various adherends while exhibiting sufficient transparency. In particular, excellent adhesion to glass can be exhibited.

The present invention relates to a tackifier containing a specific low molecular weight acrylic polymer having an amide group and / or an amino group as a constituent component, a pressure-sensitive adhesive composition containing the same, and a pressure-sensitive adhesive using the pressure-sensitive adhesive composition. Regarding products.
The present invention will be described in detail below. In the present specification, “(co) polymer” means a homopolymer and / or copolymer, and “(meth) acryl” means acryl and / or methacryl.

The tackifier and the pressure-sensitive adhesive composition of the present invention will be described in detail.
The tackifier of the present invention contains a vinyl polymer having a vinyl monomer having an amide group and / or an amino group as an essential structural unit.
Examples of the monomer having an amide group include heterocycle-containing compounds such as N-vinylpyrrolidone, N-vinylcaprolactam, and (meth) acryloylmorpholine; (meth) acrylamide, N-methyl (meth) acrylamide, N -Isopropyl (meth) acrylamide, N, N-dimethyl (meth) acrylamide, N, N-acetone (meth) acrylamide, N- (hydroxymethyl) (meth) acrylamide, N- (butoxymethyl) (meth) acrylamide, etc. (Meth) acrylamide compounds; N-vinylformamide, N-vinylacetamide, and the like are mentioned, but not limited thereto. These may be used alone or in combination of two or more.
Among these, it is preferable because the adhesive strength of the pressure-sensitive adhesive composition containing the tackifier for obtaining (meth) acryloylmorpholine and (meth) acrylamide tends to be high.

Examples of the monomer having an amino group include dimethylaminomethyl (meth) acrylate, diethylaminomethyl (meth) acrylate, dimethylaminoethyl (meth) acrylate, diethylaminoethyl (meth) acrylate, (meth) Di-n-propylaminoethyl acrylate, 2-dimethylaminopropyl (meth) acrylate, 2-diethylaminopropyl (meth) acrylate, 2- (di-n-propylamino) propyl (meth) acrylate, (meth ) 3-dimethylaminopropyl acrylate, 3-diethylaminopropyl (meth) acrylate, 3- (di-n-propylamino) propyl (meth) acrylate, and the like. These compounds may be used alone or in combination of two or more.
Among these, dimethylaminomethyl (meth) acrylate and dimethylaminoethyl (meth) acrylate are preferable because the adhesive strength of a pressure-sensitive adhesive composition containing a tackifier tends to increase.

The vinyl polymer in the present invention contains the above amide group and / or amino group-containing vinyl monomer in a range of more than 10% by mass and 90% by mass or less in the total constituent units, and 15 to 70% by mass. Is preferable, and 20-50 mass% is more preferable. When the ratio of the monomer having an amide group and / or amino group is less than 10% by mass, the interaction with the adherend is not sufficient, and the adhesion with the adherend becomes insufficient, and the adhesive strength is sufficient. May not improve. On the other hand, when it exceeds 90 mass%, compatibility with an acrylic adhesive polymer will worsen.
In the present invention, either one or both of the monomer having an amide group and the monomer having an amino group can be used. However, since higher adhesive strength may be obtained, the amide group is It is preferable to use the monomer which has.

In addition to the vinyl monomer having the amide group and / or amino group, the vinyl polymer can use other vinyl monomers copolymerizable with these as a constituent monomer. The vinyl monomer is not particularly limited. For example, methyl (meth) acrylate, ethyl (meth) acrylate, n-propyl (meth) acrylate, isopropyl (meth) acrylate, (meth ) N-butyl acrylate, isobutyl (meth) acrylate, tert-butyl (meth) acrylate, amyl (meth) acrylate, n-hexyl (meth) acrylate, n-octyl (meth) acrylate, (meth ) 2-ethylhexyl acrylate, n-nonyl (meth) acrylate, isononyl (meth) acrylate, n-decyl (meth) acrylate, n-dodecyl (meth) acrylate, n-octadecyl (meth) acrylate, etc. (Meth) acrylic acid alkyl esters of (meth) acrylic acid, itaconic acid, maleic acid, fumaric acid, etc. Tylene unsaturated carboxylic acid monomer; styrene, α-methyl styrene, o-methyl styrene, p-methyl styrene, vinyl toluene, β-methyl styrene, ethyl styrene, p-tert-butyl styrene, vinyl xylene, vinyl naphthalene Vinyl aromatic monomers such as cyclohexyl (meth) acrylate, methyl cyclohexyl (meth) acrylate, t-butylcyclohexyl (meth) acrylate, cyclododecyl (meth) acrylate, isobornyl (meth) acrylate, etc. An aliphatic cyclic vinyl monomer; phenyl (meth) acrylate, benzyl (meth) acrylate, and the like. These compounds may be used alone or in combination of two or more.
Among these, from the point that a tackifier excellent in adhesive strength is obtained, an alkyl group having 1 to 3 carbon atoms such as methyl (meth) acrylate, ethyl (meth) acrylate, n-propyl (meth) acrylate, etc. Preferred are alkyl acrylates having styrene; styrene, α-methylstyrene, cyclohexyl (meth) acrylate and isobornyl (meth) acrylate.

  The glass transition temperature (Tg) of the vinyl polymer needs to be 40 to 150 ° C, preferably 60 to 120 ° C. In the present invention, a value measured by DSC at a heating rate of 10 ° C./min is adopted as Tg. When Tg is less than 40 ° C., the adhesion strength to various adherends may be insufficient. Moreover, generally 150 degreeC is not exceeded from the restrictions of a raw material monomer, etc.

The number average molecular weight (Mn) of the vinyl polymer needs to be 500 to 10,000, preferably 500 to 7,000, and more preferably 1,000 to 5,000. When Mn exceeds 10,000, compatibility with an acrylic adhesive polymer will worsen. On the other hand, in order to produce a polymer having an Mn of less than 500, there are problems such as requiring a large amount of a polymerization initiator and a chain transfer agent, or causing a decrease in productivity.
Further, the ratio (Mw / Mn) between the weight average molecular weight (Mw) and the above (Mn) is preferably 3.0 or less, more preferably 2.2 or less, from the viewpoint that good adhesive strength is easily obtained. 1.8 or less is more preferable.
Here, the number average molecular weight Mn is a standard polystyrene conversion value obtained using gel permeation chromatography (GPC).

The vinyl polymer of the present invention is not particularly limited with respect to its production method, but can be easily obtained by polymerizing the above monomers by employing a known radical polymerization method such as a solution polymerization method, for example. .
In the case of the solution polymerization method, an organic solvent, a vinyl monomer having an amide group and / or an amino group, and other monomers are charged into a reactor, and a thermal polymerization initiator such as an organic peroxide or an azo compound is added. And the target vinyl polymer can be obtained by heating to 50-300 degreeC and copolymerizing. The vinyl polymer may be used as a solution dissolved in an organic solvent, or may be used by distilling off the solvent by heating and decompression treatment or the like.
The charging method of each raw material including the monomer may be batch initial batch charging in which all raw materials are charged at once, or semi-continuous charging in which at least one raw material is continuously fed into the reactor. A continuous polymerization method in which the raw materials are continuously supplied and the product resin is continuously withdrawn from the reactor may be used.

  As the organic solvent used in the solution polymerization method, organic hydrocarbon compounds are suitable, cyclic ethers such as tetrahydrofuran and dioxane, aromatic hydrocarbon compounds such as benzene, toluene and xylene, ethyl acetate and butyl acetate and the like. Examples include esters, ketones such as acetone, methyl ethyl ketone, and cyclohexanone, and alcohols such as methyl orthoformate, methyl orthoacetate, methanol, ethanol, and isopropanol. One or more of these can be used. Among these polymerization solvents, ethyl acetate, butyl acetate, acetone, and methyl ethyl ketone, which have a relatively low boiling point so as to dissolve the vinyl polymer well and facilitate purification, are preferable.

  The initiator used in the present invention may be an azo compound, an organic peroxide, an inorganic peroxide, or the like, but is not limited. A chain transfer agent can also be used in combination.

  Examples of the azo compound include 2,2′-azobis (isobutyronitrile), 1,1-azobis (cyclohexane-1-carbonitrile), azocumene, and 2,2′-azobis (2-methylbutyronitrile). 2,2′-azobisdimethylvaleronitrile, 4,4′-azobis (4-cyanovaleric acid), 2- (tert-butylazo) -2-cyanopropane, 2,2′-azobis (2,4,4) 4-trimethylpentane), 2,2′-azobis (2-methylpropane), dimethyl 2,2′-azobis (2-methylpropionate) and the like.

  Examples of the organic peroxide include cyclohexanone peroxide, 3,3,5-trimethylcyclohexanone peroxide, methylcyclohexanone peroxide, 1,1-bis (tert-butylperoxy) -3,3,5-trimethylcyclohexane, 1,1-bis (tert-butylperoxy) cyclohexane, n-butyl-4,4-bis (tert-butylperoxy) valerate, cumene hydroperoxide, 2,5-dimethylhexane-2,5-dihydro Peroxide, 1,3-bis (tert-butylperoxy) -m-isopropyl) benzene, 2,5-dimethyl-2,5-di (tert-butylperoxy) hexane, diisopropylbenzene peroxide, tert-butyl Cumyl peroxide, deca Ile peroxide, lauroyl peroxide, benzoyl peroxide, 2,4-dichlorobenzoyl peroxide, bis (tert-butylcyclohexyl) peroxydicarbonate, tert-butylperoxybenzoate, 2,5-dimethyl-2,5- Examples include di (benzoylperoxy) hexane.

Examples of the inorganic peroxide include potassium persulfate, sodium persulfate, and ammonium persulfate.
Redox polymerization initiators include sodium sulfite, sodium thiosulfate, sodium formaldehyde sulfoxylate, ascorbic acid, ferrous sulfate, etc. as reducing agents, potassium peroxodisulfate, hydrogen peroxide, tert-butyl hydroper What used an oxide etc. as an oxidizing agent can be used.

  The vinyl polymer of the present invention can also be obtained by continuous polymerization in a temperature range of 180 to 350 ° C. using a stirred tank reactor. In this polymerization method, since a relatively low molecular weight vinyl polymer can be obtained without substantially using a polymerization initiator or a chain transfer agent, a polymer having a high purity is obtained. However, it is preferable because it is advantageous. When the polymerization temperature is lower than 180 ° C., a polymerization initiator and a large amount of chain transfer agent are required for the polymerization reaction, and the obtained copolymer is easily colored and generates an unpleasant odor. On the other hand, when the polymerization temperature exceeds 350 ° C., a decomposition reaction is likely to occur during the polymerization reaction, and the resulting copolymer is colored, so that the transparency of the pressure-sensitive adhesive layer obtained from the pressure-sensitive adhesive composition containing this is lowered. Is concerned. Furthermore, according to such a polymerization method, a vinyl polymer having a small molecular weight distribution range can be obtained. The polymerization initiator may be optionally used, but it is preferably used at about 1% by weight or less based on the total monomers.

The pressure-sensitive adhesive composition according to the present invention includes the tackifier and the acrylic pressure-sensitive adhesive polymer described above. Here, the acrylic adhesive polymer is a polymer containing (meth) acrylic acid alkyl ester or methoxyethyl acrylate as a main constituent unit. Further, the glass transition temperature (Tg) is a polymer having adhesiveness in the range of −75 to −30 ° C., preferably in the range of −75 to −40 ° C. When Tg is less than −75 ° C., the cohesive strength of the resulting pressure-sensitive adhesive tends to be insufficient and curved surface adhesion tends to deteriorate, and when it exceeds −30 ° C., particularly when the adhesive strength at low temperatures is not sufficient. There is.
Further, the acrylic tacky polymer preferably has a weight average molecular weight (Mw) of 100,000 or more and 250,000 or more from the viewpoint of exhibiting sufficient cohesive force and good adhesiveness. More preferably, it is more preferably 400,000 or more.

  The monomer constituting the acrylic adhesive polymer is a (meth) acrylic acid alkyl ester having an alkyl group having 4 to 12 carbon atoms in that an acrylic copolymer having a low Tg and having an adhesive property is obtained. Use is preferred, for example, n-butyl (meth) acrylate, isobutyl (meth) acrylate, n-hexyl (meth) acrylate, n-octyl (meth) acrylate, isooctyl (meth) acrylate, (meth) acrylic 2-ethylhexyl acid, n-nonyl (meth) acrylate, isononyl (meth) acrylate, n-decyl (meth) acrylate, lauryl (meth) acrylate, and the like. Preferred monomers are (meth) N-butyl acrylate, 2-ethylhexyl (meth) acrylate, n-octyl (meth) acrylate, (meth) acrylic acid Sookuchiru, (meth) acrylic acid n- nonyl include isononyl (meth) acrylic acid.

  The amount of the (meth) acrylic acid alkyl ester having an alkyl group having 4 to 12 carbon atoms is preferably 30 to 100% by mass, and preferably 50 to 99% by mass based on all constituent monomers of the acrylic copolymer. Is more preferable. When the amount is less than 30% by mass, the resulting adhesive composition has insufficient adhesive strength, tackiness, low-temperature adhesiveness, and the like.

  As the acrylic adhesive polymer, in addition to the above (meth) acrylic acid alkyl ester, other monomers copolymerizable therewith can be used as long as the adhesive performance is not impaired. Examples of the copolymerizable monomer include α, β-ethylenically unsaturated carboxylic acid monomers such as (meth) acrylic acid, itaconic acid, maleic acid and fumaric acid; methyl (meth) acrylate, (meth ) (Meth) acrylic acid alkyl ester having an alkyl group having 1 to 3 carbon atoms such as ethyl acrylate, n-propyl (meth) acrylate, isopropyl (meth) acrylate, etc .; styrene, α-methylstyrene, vinyltoluene, etc. Vinyl aromatic monomers such as cyclohexyl (meth) acrylate, methyl cyclohexyl (meth) acrylate, t-butylcyclohexyl (meth) acrylate, cyclododecyl (meth) acrylate, isobornyl (meth) acrylate, etc. Aliphatic cyclic vinyl monomer; unsaturated dicarbonate such as itaconic acid monoethyl ester, fumaric acid monobutyl ester Monoalkyl ester of boric acid; 2-hydroxyethyl (meth) acrylate, 3-hydroxypropyl (meth) acrylate, 4-hydroxybutyl (meth) acrylate, polyethylene glycol (meth) acrylate, polypropylene glycol (meth) acrylate And hydroxyl group-containing monomers such as polyethylene-polypropylene glycol mono (meth) acrylate; ethylenically unsaturated carboxylic acid amides such as acrylamide, N-methylolacrylamide, N-methoxymethylacrylamide, N-methoxybutylacrylamide, and N-substituted compounds Unsaturated alcohols such as allyl alcohol; (meth) acrylonitrile, vinyl acetate, glycidyl (meth) acrylate, diacetone acrylamide, etc., and one of these It is possible to use more than seeds.

  The acrylic adhesive polymer can also be obtained by a known radical polymerization method such as a solution polymerization method, a suspension polymerization method, or an emulsion polymerization method.

The pressure-sensitive adhesive composition of the present invention is not particularly limited in its mixing method as long as it contains the tackifier containing the vinyl polymer and the acrylic tacky polymer. For example, the tackifier and acrylic A method of mixing an adhesive polymer may be used, or a method obtained by polymerizing an acrylic adhesive polymer in the presence of a tackifier.
The content of the tackifier in the pressure-sensitive adhesive composition is preferably 5 to 60 parts by mass, more preferably 5 to 40 parts by mass with respect to 100 parts by mass of the acrylic adhesive polymer. Yes, more preferably 5 to 30 parts by mass. Adhesive strength to various adherends tends to be sufficiently improved when the amount of tackifier used is 5 parts by mass or more, and good adhesion including initial adhesive strength (tack) is achieved by setting it to 60 parts by mass or less. Strength can be obtained.

  The pressure-sensitive adhesive composition of the present invention includes a crosslinking agent (curing agent), another tackifier, a plasticizer, an antioxidant, and an ultraviolet absorber as necessary in addition to the above-described tackifier and acrylic tacky polymer. Further, the composition may contain an additive such as an anti-aging agent, a flame retardant, a fungicide, a silane coupling agent, a filler, and a colorant.

  Examples of the crosslinking agent (curing agent) include a glycidyl compound having two or more glycidyl groups, an isocyanate compound having two or more isocyanate groups, an aziridine compound having two or more aziridinyl groups, an oxazoline compound having an oxazoline group, and a metal chelate compound. And butylated melamine compounds. Of these, aziridine compounds, glycidyl compounds and isocyanate compounds are preferred.

  Examples of the aziridine compound include 1,6-bis (1-aziridinylcarbonylamino) hexane, 1,1 ′-(methylene-di-p-phenylene) bis-3,3-aziridylurea, 1,1′-. (Hexamethylene) bis-3,3-aziridylurea, ethylenebis- (2-aziridinylpropionate), tris (1-aziridinyl) phosphine oxide, 2,4,6-triaziridinyl-1,3,5- And triazine, trimethylolpropane-tris- (2-aziridinylpropionate), and the like.

  Examples of the glycidyl compound include ethylene glycol diglycidyl ether, polyethylene glycol diglycidyl ether, propylene glycol diglycidyl ether, polypropylene glycol diglycidyl ether, glycerin diglycidyl ether, neopentyl glycol diglycidyl ether, and 1,6-hexanediol diglycidyl. Ether, tetraglycidylxylenediamine, 1,3-bis (N, N-diglycidylaminomethyl) cyclohexane, trimethylolpropane polyglycidyl ether, diglycerol polyglycidyl ether, polyglycerol polyglycidyl ether, sorbitol polyglycidyl ether A functional glycidyl compound is mentioned.

As the isocyanate compound, a compound having two or more isocyanate groups is preferably used.
As the isocyanate compound, aromatic, aliphatic and alicyclic isocyanate compounds, and modified products (such as prepolymers) of these isocyanate compounds can be used.

As aromatic isocyanate, diphenylmethane diisocyanate (MDI), crude diphenylmethane diisocyanate, tolylene diisocyanate, naphthalene diisocyanate (NDI), p-phenylene diisocyanate (PPDI), xylene diisocyanate (XDI), tetramethylxylylene diisocyanate (TMXDI), tolidine A diisocyanate (TODI) etc. are mentioned.
Examples of the aliphatic isocyanate include hexamethylene diisocyanate (HDI), lysine diisocyanate (LDI), and lysine triisocyanate (LTI).
Examples of the alicyclic isocyanate include isophorone diisocyanate (IPDI), cyclohexyl diisocyanate (CHDI), hydrogenated XDI (H6XDI), and hydrogenated MDI (H12MDI).
The modified isocyanate includes urethane modified products, dimers, trimers, carbodiimide modified products, allophanate modified products, burette modified products, urea modified products, isocyanurate modified products, oxazolidone modified products, isocyanates. Examples thereof include base end prepolymers.

  When the pressure-sensitive adhesive composition of the present invention contains a crosslinking agent (curing agent), the content thereof is preferably 0.01 to 10 parts by mass with respect to 100 parts by mass of the (meth) acrylic adhesive polymer. More preferably, it is 0.03-5 mass parts, More preferably, it is 0.05-2 mass parts.

  Examples of the other tackifiers include rosin derivatives such as rosin ester, gum rosin, tall oil rosin, hydrogenated rosin ester, maleated rosin, and disproportionated rosin ester; terpene phenol resin, α-pinene, β-pinene, Examples include terpene resins mainly composed of limonene and the like; (hydrogenated) petroleum resins; coumarone-indene resins; hydrogenated aromatic copolymers; styrene resins; phenol resins;

  Examples of the plasticizer include phthalic acid esters such as di-n-butyl phthalate, di-n-octyl phthalate, bis (2-ethylhexyl) phthalate, di-n-decyl phthalate, diisodecyl phthalate; bis (2-ethylhexyl) adipate, di Adipic acid esters such as n-octyl adipate; Sebacic acid esters such as bis (2-ethylhexyl) sebacate, di-n-butyl sebacate; Azelaic acid esters such as bis (2-ethylhexyl) azelate; Paraffin such as chlorinated paraffin Glycols such as polypropylene glycol; epoxy-modified vegetable oils such as epoxidized soybean oil and epoxidized linseed oil; phosphate esters such as trioctyl phosphate and triphenyl phosphate; phosphorous acid s such as triphenyl phosphite Ester compounds such as esterified products of adipic acid and 1,3-butylene glycol; low molecular weight polymers such as low molecular weight polybutene, low molecular weight polyisobutylene, and low molecular weight polyisoprene; process oils, naphthenic oils, etc. Examples thereof include oils.

  Examples of the antioxidant include 2,6-di-tert-butyl-p-cresol, butylated hydroxyanisole, 2,6-di-tert-butyl-4-ethylphenol, stearyl-β- (3,5- Di-tert-butyl-4-hydroxyphenyl) propionate, 2,2′-methylenebis (4-methyl-6-tert-butylphenol), 2,2′-methylenebis (4-ethyl-6-tert-butylphenol), 4 , 4′-thiobis (3-methyl-6-tert-butylphenol), 4,4′-butylidenebis (3-methyl-6-tert-butylphenol), 3,9-bis [1,1-dimethyl-2- [ β- (3-tert-butyl-4-hydroxy-5-methylphenyl) propionyloxy] ethyl] 2,4,8,10-te Traoxaspiro [5.5] undecane, 1,3-tris (2-methyl-4-hydroxy-5-tert-butylphenyl) butane, 1,3,5-trimethyl-2,4,6-tris (3 , 5-di-tert-butyl-4-hydroxybenzyl) benzene, tetrakis- [methylene-3- (3 ′, 5′-di-tert-butyl-4′-hydroxyphenyl) propionate] methane, bis [3, 3′-bis- (4′-hydroxy-3′-tert-butylphenyl) butyric acid] glycol ester, 1,3,5-tris (3 ′, 5′-di-tert-butyl-4′-hydroxy Benzyl) -S-triazine-2,4,6- (1H, 3H, 5H) trione, tocopherols and other phenolic antioxidants; dilauryl 3,3′-thiodi Sulfur antioxidants such as lopionate, dimyristyl 3,3′-thiodipropionate, stearyl 3,3′-thiodipropionate; triphenyl phosphite, diphenylisodecyl phosphite, 4,4′-butylidene-bis (3-methyl-6-tert-butylphenylditridecyl) phosphite, cyclic neopentanetetraylbis (octadecyl phosphite), tris (nonylphenyl) phosphite, tris (monononylphenyl) phosphite, tris (di Nonylphenyl) phosphite, diisodecylpentaerythritol diphosphite, 9,10-dihydro-9-oxa-10-phosphaphenanthrene-10-oxide, 10- (3,5-di-tert-butyl-4-hydroxybenzyl -9, 1 -Dihydro-9-oxa-10-phosphaphenanthrene-10-oxide, 10-decyloxy-9,10-dihydro-9-oxa-10-phosphaphenanthrene, tris (2,4-di-tert-butylphenyl) Phosphite, cyclic neopentanetetrayl bis (2,4-di-tert-butylphenyl) phosphite, cyclic neopentanetetrayl bis (2,6-di-tert-butyl-4-methylphenyl) phosphite And phosphorus antioxidants such as 2,2-methylenebis (4,6-di-tert-butylphenyl) octyl phosphite.

  Examples of the UV absorber include salicylic acid UV absorbers such as phenyl salicylate, p-tert-butylphenyl salicylate, and p-octylphenyl salicylate; 2,4-dihydroxybenzophenone, 2-hydroxy-4-methoxybenzophenone, 2-hydroxy -4-octoxybenzophenone, 2-hydroxy-4-dodecyloxybenzophenone, 2,2'-dihydroxy-4-methoxybenzophenone, 2,2'-dihydroxy-4,4'-dimethoxybenzophenone, 2-hydroxy-4- Benzophenone ultraviolet absorbers such as methoxy-5-sulfobenzophenone and bis (2-methoxy-4-hydroxy-5-benzoylphenyl) methane; 2- (2′-hydroxy-5′-methylphenyl) benzotriazole, 2- 2'-hydroxy-5'-tert-butylphenyl) benzotriazole, 2- (2'-hydroxy-3 ', 5'-di-tert-butylphenyl) benzotriazole, 2- (2'-hydroxy-3' -Tert-butyl-5'-methylphenyl) -5-chlorobenzotriazole, 2- (2'-hydroxy-3 ', 5'-di-tert-butylphenyl) -5-chlorobenzotriazole, 2- (2 '-Hydroxy-3', 5'-di-tert-amylphenyl) benzotriazole, 2- (2'-hydroxy-4'-octoxyphenyl) benzotriazole, 2- [2'-hydroxy-3 '-( 3 ", 4", 5 ", 6" -tetrahydrophthalimidomethyl) -5'-methylphenyl] benzotriazole, 2,2-methylenebis 4- (1,1,3,3-tetramethylbutyl) -6- (2H-benzotriazol-2-yl) phenol], 2- (2′-hydroxy-5′-methacryloxyphenyl) -2H-benzo Benzotriazole ultraviolet absorbers such as triazole and 2,2′-methylenebis [4- (1,1,3,3-tetramethylbutyl) -6- (2H-benzotriazol-2-yl) phenol]; Cyanoacrylate ultraviolet absorbers such as ethylhexyl-2-cyano-3,3′-diphenylacrylate, ethyl-2-cyano-3,3′-diphenylacrylate; nickel bis (octylphenyl) sulfide, [2,2′- Thiobis (4-tert-octylphenolate)]-n-butylamine nickel, nickel complex-3,5-di Examples thereof include nickel-based UV stabilizers such as -tert-butyl-4-hydroxybenzyl-phosphate monoethylate and nickel-dibutyldithiocarbamate.

  Examples of the anti-aging agent include poly (2,2,4-trimethyl-1,2-dihydroquinoline), 6-ethoxy-1,2-dihydro-2,2,4-trimethylquinoline, and 1- (N-phenyl). Amino) -naphthalene, styrenated diphenylamine, dialkyldiphenylamine, N, N′-diphenyl-p-phenylenediamine, N-phenyl-N′-isopropyl-p-phenylenediamine, N, N′-di-2-naphthyl-p -Phenylenediamine, 2,6-di-tert-butyl-4-methylphenol, mono (α-methylbenzyl) phenol, di (α-methylbenzyl) phenol, tri (α-methylbenzyl) phenol, 2,2 ′ -Methylenebis (4-methyl-6-tert-butylphenol), 2,2'-methylenebis (4-ethyl- -Tert-butylphenol), 4,4'-butylidenebis (6-tert-butyl-3-methylphenol), 4,4'-thiobis (6-tert-butyl-3-methylphenol), 1,1-bis ( 4-hydroxyphenyl) cyclohexane, 2,5-di-tert-butylhydroquinone, 2,5-di-tert-amylhydroquinone, 2-mercaptobenzimidazole, zinc salt of 2-mercaptobenzimidazole, 2-mercaptomethylbenzimidazole , Nickel dibutyldithiocarbamate, tris (nonylphenyl) phosphite, dilauryl thiodipropionate, distearyl thiodipropionate, and the like.

  Examples of the flame retardant include tetrabromobisphenol A, 2,2-bis (4-hydroxy-3,5-dibromophenyl) propane, hexabromobenzene, tris (2,3-dibromopropyl) isocyanurate, 2,2- Halogen flame retardants such as bis (4-hydroxyethoxy-3,5-dibromophenyl) propane, decabromodiphenyl oxide, halogen-containing polyphosphate; ammonium phosphate, tricresyl phosphate, triethyl phosphate, tris (β-chloroethyl) ) Phosphorus flame retardants such as phosphate, trischloroethyl phosphate, trisdichloropropyl phosphate, cresyl diphenyl phosphate, xylenyl diphenyl phosphate, acidic phosphate ester, nitrogen-containing phosphorus compounds; red phosphorus, tin oxide, trioxide Inorganic flame retardants such as Ntimmon, zirconium hydroxide, barium metaborate, aluminum hydroxide, magnesium hydroxide; poly (dimethoxysiloxane), poly (diethoxysiloxane), poly (diphenoxysiloxane), poly (methoxyphenoxysiloxane) Siloxane flame retardants such as methyl silicate, ethyl silicate, and phenyl silicate.

  Examples of the antifungal agent include benzimidazole, benzothiazole, trihaloallyl, triazole, and organic nitrogen sulfur compounds.

  Examples of the silane coupling agent include vinyltriethoxysilane, vinyltris (β-methoxyethoxy) silane, γ-methacryloxypropyltrimethoxysilane, vinyltriacetoxysilane, γ-glycidoxypropyltrimethoxysilane, and γ-glycid. Xylpropyltriethoxysilane, β- (3,4-epoxycyclohexyl) ethyltrimethoxysilane, γ-chloropropylmethoxysilane, vinyltrichlorosilane, γ-mercaptopropyltrimethoxysilane, γ-aminopropyltriethoxysilane, N- β (aminoethyl) -γ-aminopropyltrimethoxysilane and the like can be mentioned.

  Examples of the filler include inorganic powder fillers such as calcium carbonate, titanium oxide, mica and talc; fibrous fillers such as glass fibers and organic reinforcing fibers.

If the adhesive composition of this invention contains the said acrylic adhesive polymer and the said tackifier, there will be no restriction | limiting in particular in the form. For example, it may be used as a form of a solvent-type pressure-sensitive adhesive composition dissolved in an organic solvent such as ethyl acetate, or a form of an emulsion-type pressure-sensitive adhesive composition in which an acrylic pressure-sensitive adhesive polymer and a tackifier are dispersed in an aqueous medium. It may be used as
In the case of the solution-type pressure-sensitive adhesive composition and the emulsion-type pressure-sensitive adhesive composition, the medium such as an organic solvent or water used is usually 20 to 80 parts by mass with respect to 100 parts by mass of the pressure-sensitive adhesive composition.

  When used as an emulsion-type pressure-sensitive adhesive, a stabilizer can be blended. This stabilizer is used for vinyl chloride such as cadmium stearate, zinc stearate, barium stearate, calcium stearate, lead dibutyltin dilaurate, tris (nonylphenyl) phosphite, triphenylphosphite, diphenylisodecylphosphite, etc. Stabilizer; di-n-octyltin bis (isooctylthioglycolate) salt, di-n-octyltin maleate polymer, di-n-octyltin dilaurate, di-n-octyltin maleate Ester salt, di-n-butyltin bismaleic acid ester salt, di-n-butyltin maleate polymer, di-n-butyltin bisoctylthioglycol ester salt, di-n-butyltin β-mercaptopropionate polymer, di -N-Butyl tin dilaure Di-n-methyltin bis (isooctyl mercaptoacetate) salt, poly (thiobis-n-butyltin sulfide), monooctyltin tris (isooctylthioglycolate ester), dibutyltin maleate, di-n-butyltin maleate ester・ Carboxylate and di-n-butyltin malate ester ・ Organic tin stabilizers such as mercaptides; tribasic lead sulfate, dibasic lead phosphite, basic lead sulfite, dibasic lead phthalate, silica Lead stabilizers such as lead acid, dibasic lead stearate, lead stearate; metal soap stabilizers such as cadmium soap, zinc soap, barium soap, lead soap, composite metal soap, calcium stearate Etc.

In addition, the pressure-sensitive adhesive composition of the present invention includes a monofunctional and / or polyfunctional (meth) acrylic acid monomer, and a photopolymerization initiator in addition to the acrylic pressure-sensitive adhesive polymer and the tackifier. By using a composition containing the above, etc., it may be used in the form of a photocurable pressure-sensitive adhesive composition that is cured by active energy rays such as ultraviolet rays.
The tackifier of the present invention does not cause curing inhibition during UV curing, unlike general tackifier resins such as rosin resins and terpene resins. For this reason, when used for a photocurable pressure-sensitive adhesive composition such as UV curing, the adhesive properties such as adhesive strength can be improved without adversely affecting the curability.

  In the case of the photocurable pressure-sensitive adhesive composition, the composition may contain an organic solvent or the like, but is generally used as a solventless type containing no solvents.

  Examples of the monofunctional (meth) acrylic acid monomers include (meth) acrylic acid alkyl esters having an alkyl group having 1 to 12 carbon atoms; (meth) acrylic acid cyclohexyl, (meth) acrylic acid dicyclopentyl, ( (Meth) acrylic esters having a cyclic structure such as isobornyl (meth) acrylate; hydroxy (meth) acrylates such as hydroxyethyl (meth) acrylate, hydroxypropyl (meth) acrylate, hydroxybutyl (meth) acrylate Alkyl esters; (meth) acrylic acid and the like. These compounds may be used alone or in combination of two or more.

  Examples of the polyfunctional (meth) acrylic acid monomer include di (meth) acrylates of alkylene glycol such as butanediol di (meth) acrylate and hexanediol di (meth) acrylate; di (meth) triethylene glycol Di (meth) acrylates of polyalkylene glycols such as acrylates; trimethylolpropane tri (meth) acrylate and its ethylene oxide and / or propylene oxide modified products, pentaerythritol tri (meth) acrylate, pentaerythritol tetra (meth) acrylate, etc. Is mentioned. These compounds may be used alone or in combination of two or more.

  The content of the tackifier in the photocurable pressure-sensitive adhesive composition is preferably 5 to 100 parts by mass with respect to the acrylic pressure-sensitive adhesive polymer and the monofunctional and / or polyfunctional (meth) acrylic acid monomer. 60 mass parts, More preferably, it is 5-40 mass parts, More preferably, it is 5-30 mass parts.

Examples of the photopolymerization initiator include benzoin and its alkyl ethers, acetophenones, anthraquinones, thioxanthones, ketals, benzophenones, xanthones, acylphosphine oxides, α-diketones and the like.
Moreover, in order to improve the sensitivity by an active energy ray, a photosensitizer can also be used together.
Examples of the photosensitizer include benzoic acid and amine photosensitizers. These can also be used in combination of two or more.
As for the usage-amount of a photoinitiator and a photosensitizer, 0.01-10 mass parts is preferable with respect to 100 mass parts of monofunctional and / or polyfunctional (meth) acrylic-acid type monomers.

  As the photocurable resin composition containing the tackifier of the present invention, in addition to the photocurable adhesive composition described above, the tackifier, monofunctional and / or polyfunctional (meth) acrylic acid is used. It can also be used as a photocurable adhesive composition comprising a system monomer and a composition containing a photopolymerization initiator. The said acrylic adhesive polymer can be mixed with the said photocurable adhesive composition as needed.

  The pressure-sensitive adhesive composition of the present invention is suitably used for laminating applications when forming laminates such as various optical films in addition to various general pressure-sensitive processed products such as pressure-sensitive adhesive films, pressure-sensitive adhesive sheets, pressure-sensitive adhesive tapes, and labels. be able to.

  Further, when used as a photo-curing adhesive, it can be suitably used as an adhesive for producing a laminate constituting an optical disk and various optical displays.

When applied to the above general pressure-sensitive processed product, after applying the pressure-sensitive adhesive composition of the present invention to one or both surfaces of various substrates, a pressure-sensitive adhesive layer is formed by irradiating active energy rays such as drying or UV, It can be set as an adhesive product such as an adhesive sheet or an adhesive tape. Moreover, the product which has an adhesion layer can also be obtained by making a composition into a molten state, applying to a base material, and cooling.
As the substrate, papers, films, cloths, nonwoven fabrics, metal foils, and the like can be used. The pressure-sensitive adhesive composition may be applied directly to these substrates, or applied to a release paper or the like. After being worked and dried, it may be transferred to a substrate.
The thickness (thickness after drying) of the pressure-sensitive adhesive formed on the pressure-sensitive adhesive sheet is selected depending on the application, but is usually in the range of 1 to 300 μm, preferably in the range of 5 to 250 μm, and further in the range of 10 to 200 μm. preferable.

  Specific examples of the general adhesive processed product include an adhesive sheet, an adhesive film, an adhesive tape, a pressure sensitive tape, a surface protective film, a surface protective tape, a masking tape, an electrical insulating tape, and a laminate.

  Since the pressure-sensitive adhesive composition of the present invention is excellent in transparency and has high adhesive strength to various adherends including glass, such as touch panels, liquid crystal display devices, organic EL display devices, plasma display panels, etc. It is also suitable for bonding a display and various optical films used therefor. Moreover, it is useful also for the adhesive use in electronic components, such as a flexible printed circuit board.

Hereinafter, the present invention will be specifically described based on examples. In addition, this invention is not limited to the following Example. In the following description, “part” means part by mass, and “%” means mass%.
In addition, various analyzes of the polymer obtained in this example were performed by the methods described below.

<Solid content>
About 1 g of the measurement sample was weighed (a), then the residue after drying at 155 ° C. for 30 minutes in the ventilation dryer was measured (b) and calculated from the following formula. A weighing bottle was used for the measurement. Other operations were in accordance with JIS K 0067-1992 (chemical product weight loss and residue test method).
Solid content (%) = (b / a) × 100

<Molecular weight measurement>
The molecular weight was measured by GPC under the following conditions.
GPC: Tosoh (HLC-8120)
Column: Tosoh (TSKgel-Super MP-M x 4)
Sample concentration: 0.1%
Flow rate: 0.6 ml / min Eluent: Tetrahydrofuran Column temperature: 40 ° C
Detector: Suggested refractometer (RI)
Reference material: Polystyrene

<Glass transition point (Tg)>
Tg was measured by DSC under the following conditions.
DSC: manufactured by TA Instrument (Q-100)
Temperature rise: 10 ° C / min Measurement atmosphere: Nitrogen

<Polymer composition>
The polymer composition was calculated from the monomer charge and the monomer consumption by GC measurement.
GC: Made by Agilent Technologies (7820A GC System)
Detector: FID
Column: 100% dimethylsiloxane (CP-Sil 5CB) Length 30m, inner diameter 0.32mm
Calculation method: Internal standard method

1. Synthetic Synthesis Example 1 of Vinyl Polymer (Synthesis of Polymer A-1)
In a four-necked flask with an internal volume of 1 liter, 200 parts by mass of dimethylformamide (hereinafter referred to as “DMF”) and dimethyl 2,2′-azobis (2-methylpropionate) (made by Wako Pure Chemical Industries, Ltd., trade name “ V-601 ")) was mixed with 6.8 parts by mass, this mixture was sufficiently degassed by bubbling nitrogen gas, and the internal temperature of the mixture was increased to 90 ° C. Separately, a dropping funnel containing a mixture of 48 parts by weight of methyl methacrylate (hereinafter referred to as “MMA”), 194 parts by weight of acryloylmorpholine (hereinafter referred to as “ACMO”), 90 parts by weight of V-601 and 90 parts by weight of DMF is added. The polymerization was carried out by dropping into the flask over 5 hours. After completion of the dropping, the polymerization solution was dropped into a mixed solution consisting of 4200 parts by mass of hexane and 1800 parts by mass of ethyl acetate to isolate the vinyl polymer in the polymerization solution, thereby obtaining a polymer A-1. The obtained polymer A-1 consisted of the composition calculated from the charged amount and the monomer consumption by GC measurement, 70% by mass of ACMO and 30% by mass of MMA, and was Mw2390, Mn1570, Mw / Mn1.52. The Tg was 86 ° C.

Synthesis Example 2 (Synthesis of Polymer A-2)
A mixed solution consisting of 180 parts by mass of DMF and 4.4 parts by mass of V-601 was charged into a 4-liter flask having an internal volume of 1 liter, and this mixture was sufficiently degassed by bubbling with nitrogen gas. The internal temperature was raised to 90 ° C. Separately, polymerization was performed by dropping a mixed liquid consisting of 105 parts by mass of MMA, 144 parts by mass of ACMO, 84 parts by mass of V-601, and 90 parts by mass of DMF from the dropping funnel into the flask over 5 hours. After completion of the dropping, the polymerization solution was dropped into a mixed solution consisting of 4200 parts by mass of hexane and 1800 parts by mass of ethyl acetate to isolate the vinyl polymer in the polymerization solution, thereby obtaining a polymer A-2.
Table 1 shows the composition and analysis results of the polymer A-2.

Synthesis Example 3 (Synthesis of Polymer A-3)
A four-necked flask with an internal volume of 1 liter is charged with a mixed liquid consisting of 223 parts by mass of butyl acetate and 3.3 parts by mass of V-601, and the mixed liquid is sufficiently degassed by bubbling with nitrogen gas. The internal temperature was increased to 90 ° C. Separately, polymerization was performed by dropping a mixed liquid consisting of 162 parts by mass of MMA, 85 parts by mass of ACMO, 62 parts by mass of V-601, and 90 parts by mass of butyl acetate into the flask from a dropping funnel over 5 hours. After completion of the dropping, the polymerization solution was dropped into a mixed solution consisting of 4200 parts by mass of hexane and 1800 parts by mass of ethyl acetate to isolate the vinyl polymer in the polymerization solution, thereby obtaining a polymer A-3.
Table 1 shows the composition and analysis results of the polymer A-3.

Synthesis Example 4 (Synthesis of Polymer A-4)
A four-necked flask with an internal volume of 1 liter is charged with a mixed solution consisting of 255 parts by mass of butyl acetate and 1.5 parts by mass of V-601, and this mixture is sufficiently degassed by bubbling with nitrogen gas. The internal temperature was increased to 90 ° C. Separately, polymerization was carried out by dropping a mixed solution of 171 parts by mass of MMA, 79 parts by mass of ACMO, 29 parts by mass of V-601, and 90 parts by mass of butyl acetate into the flask from a dropping funnel over 5 hours. After completion of the dropwise addition, the polymerization solution was dropped into a mixed solution consisting of 4200 parts by mass of hexane and 1800 parts by mass of ethyl acetate, whereby the vinyl polymer in the polymerization solution was isolated to obtain a polymer A-4.
Table 1 shows the composition and analysis results of the polymer A-4.

Synthesis Example 5 (Synthesis of Polymer A-5)
A mixed solution consisting of 284 parts by mass of butyl acetate and 0.8 part by mass of V-601 is charged into a 4-liter flask having an internal volume of 1 liter, and this mixture is sufficiently degassed by bubbling with nitrogen gas. The internal temperature was increased to 90 ° C. Separately, polymerization was carried out by dropping a mixed liquid composed of 180 parts by mass of MMA, 80 parts by mass of ACMO, 15 parts by mass of V-601, and 90 parts by mass of butyl acetate into the flask from a dropping funnel over 5 hours. After completion of the dropwise addition, the polymerization solution was dropped into a mixed solution consisting of 4200 parts by mass of hexane and 1800 parts by mass of ethyl acetate, whereby the vinyl polymer in the polymerization solution was isolated to obtain a polymer A-5.
Table 1 shows the composition and analysis results of the polymer A-5.

Synthesis Example 6 (Synthesis of Polymer A-6)
A four-necked flask with an internal volume of 1 liter is charged with a mixed liquid consisting of 224 parts by mass of DMF and 3.1 parts by mass of V-601, and the mixed liquid is sufficiently degassed by bubbling with nitrogen gas. The internal temperature was raised to 90 ° C. Separately, by dropping a mixed liquid of 167 parts by mass of MMA, 83 parts by mass of acrylamide (hereinafter referred to as AAm), 3.1 parts by mass of V-601, and 90 parts by mass of DMF from the dropping funnel into the flask over 5 hours. Polymerization was performed. After completion of the dropwise addition, the polymerization solution was dropped into a mixed solution consisting of 4200 parts by mass of hexane and 1800 parts by mass of ethyl acetate, whereby the vinyl polymer in the polymerization solution was isolated to obtain a polymer A-6.
Table 1 shows the composition and analysis results of the polymer A-6.

Synthesis Example 7 (Synthesis of Polymer A-7)
A liquid mixture consisting of 236 parts by mass of butyl acetate and 2.5 parts by mass of V-601 is charged into a 4-liter flask having an internal volume of 1 liter, and the mixed liquid is sufficiently degassed by bubbling nitrogen gas. The internal temperature was increased to 90 ° C. Separately, a mixed liquid consisting of 170 parts by mass of MMA, 84 parts by mass of dimethylaminoethyl methacrylate (hereinafter referred to as DMA), 47 parts by mass of V-601 and 90 parts by mass of butyl acetate was dropped into the flask from the dropping funnel over 5 hours. Then, polymerization was performed. After completion of the dropwise addition, the polymerization solution was dropped into a mixed solution consisting of 4200 parts by mass of hexane and 1800 parts by mass of ethyl acetate, whereby the vinyl polymer in the polymerization solution was isolated to obtain a polymer A-7.
Table 1 shows the composition and analysis results of the polymer A-7.

Synthesis Example 8 (Synthesis of Polymer A-8)
A four-necked flask with an internal volume of 1 liter is charged with a mixed liquid consisting of 39 parts by mass of styrene (hereinafter referred to as “St”), 16 parts by mass of ACMO, 226 parts by mass of butyl acetate, and 7.1 parts by mass of V-601. The mixture was sufficiently deaerated by bubbling with nitrogen gas, and the internal temperature of the mixture was raised to 90 ° C. Separately, polymerization was performed by dropping a mixed solution of St 154 parts by mass, ACMO 44 parts by mass, V-601 52 parts by mass, and butyl acetate 90 parts by mass from the dropping funnel into the flask over 5 hours. After completion of the dropwise addition, the polymerization solution was dropped into a mixed solution consisting of 4200 parts by mass of methanol and 1800 parts by mass of water, whereby the vinyl polymer in the polymerization solution was isolated to obtain a polymer A-8.
Table 1 shows the composition and analysis results of the polymer A-8.

Synthesis Example 9 (Synthesis of Polymer A-9)
A mixed solution consisting of 220 parts by mass of butyl acetate and 3.4 parts by mass of V-601 is charged into a 4-liter flask having an internal volume of 1 liter, and this mixture is sufficiently degassed by bubbling nitrogen gas. The internal temperature was increased to 90 ° C. Separately, a mixed liquid consisting of 195 parts by mass of isobornyl methacrylate (hereinafter referred to as “IBXMA”), 56 parts by mass of ACMO, 64 parts by mass of V-601, and 90 parts by mass of butyl acetate is added from the dropping funnel into the flask over 5 hours. Polymerization was carried out by dropping. After completion of the dropping, the polymerization solution was dropped into a mixed solution consisting of 4200 parts by mass of methanol and 1800 parts by mass of water, whereby the vinyl polymer in the polymerization solution was isolated to obtain a polymer A-9.
The composition and analysis results of the polymer A-9 are shown in Table 1.

Synthesis Example 10 (Synthesis of Polymer A-10)
A four-necked flask with an internal volume of 1 liter is charged with a mixed solution consisting of 50 parts by mass of MMA, 227 parts by mass of butyl acetate and 15 parts by mass of V-601, and this mixture is sufficiently degassed by bubbling nitrogen gas. The internal temperature of the mixed solution was raised to 90 ° C. Separately, polymerization was carried out by dropping a mixed liquid consisting of 200 parts by mass of MMA, 46 parts by mass of V-601 and 90 parts by mass of butyl acetate into the flask from the dropping funnel over 5 hours. After completion of the dropping, the polymerization solution was added dropwise to 6000 parts by mass of hexane, whereby the vinyl polymer in the polymerization solution was isolated to obtain a polymer A-10.
Table 1 shows the composition and analysis results of the polymer A-10.

Synthesis Example 11 (Synthesis of Polymer A-11)
A four-necked flask with an internal volume of 1 liter was charged with a mixed liquid consisting of 19 parts by mass of MMA, 11 parts by mass of St, 220 parts by mass of butyl acetate and 9 parts by mass of V-601, and this mixed liquid was bubbled with nitrogen gas. The mixture was sufficiently deaerated, and the internal temperature of the mixed solution was raised to 90 ° C. Separately, polymerization was carried out by dropping a mixed liquid consisting of 108 parts by mass of MMA, 93 parts by mass of St, 78 parts by mass of V-601, and 90 parts by mass of butyl acetate from the dropping funnel into the flask over 5 hours. After completion of the dropwise addition, the polymerization solution was dropped into 4200 parts by mass of methanol and 1800 parts by mass of water, whereby the vinyl polymer in the polymerization solution was isolated to obtain a polymer A-11.
The composition and analysis results of the polymer A-11 are shown in Table 1.

Synthesis Example 12 (Synthesis of Polymer A-12)
A mixed liquid consisting of 180 parts by mass of DMF and 0.8 parts by mass of V-601 is charged into a 4-liter flask having an internal volume of 1 liter, and the mixed liquid is sufficiently degassed by bubbling nitrogen gas. The internal temperature was raised to 90 ° C. Separately, polymerization was carried out by dropping a mixed liquid consisting of 105 parts by mass of MMA, 144 parts by mass of ACMO, 14 parts by mass of V-601, and 90 parts by mass of DMF from the dropping funnel into the flask over 5 hours. After completion of the dropping, the polymerization solution was dropped into a mixed solution consisting of 4200 parts by mass of hexane and 1800 parts by mass of ethyl acetate to isolate the vinyl polymer in the polymerization solution, thereby obtaining a polymer A-12.
The composition and analysis results of the polymer A-12 are shown in Table 1.

Synthesis Example 13 (Synthesis of Polymer A-13)
A four-necked flask with an internal volume of 1 liter is charged with a mixed liquid consisting of 207 parts by mass of DMF and 3.1 parts by mass of V-601, and the mixed liquid is sufficiently degassed by bubbling with nitrogen gas. The internal temperature was raised to 90 ° C. Separately, a mixed liquid consisting of 131 parts by weight of butyl methacrylate (hereinafter referred to as BMA), 134 parts by weight of ACMO, 58 parts by weight of V-601, and 90 parts by weight of DMF is dropped from the dropping funnel into the flask over 5 hours. Polymerization was performed. After completion of the dropping, the polymerization solution was dropped into a mixed solution consisting of 4200 parts by mass of hexane and 1800 parts by mass of ethyl acetate, whereby the vinyl polymer in the polymerization solution was isolated to obtain a polymer A-13.
The composition and analysis results of the polymer A-13 are shown in Table 1.

Synthesis Example 14 (Synthesis of Polymer A-14)
A four-necked flask with an internal volume of 1 liter is charged with a mixed liquid consisting of 200 parts by mass of DMF and 3.8 parts by mass of V-601, and the mixed liquid is sufficiently degassed by bubbling nitrogen gas. The internal temperature was raised to 90 ° C. Separately, polymerization was carried out by dropping a mixed liquid consisting of 237 parts by mass of MMA, 15 parts by mass of ACMO, 67 parts by mass of V-601, and 90 parts by mass of DMF from the dropping funnel into the flask over 5 hours. After completion of the dropping, the polymerization solution was dropped into a mixed solution composed of 6000 parts by mass of hexane, whereby the vinyl polymer in the polymerization solution was isolated to obtain a polymer A-14.
The composition and analysis results of the polymer A-14 are shown in Table 1.

2. Synthesis Synthesis Example 15 of Acrylic Adhesive Polymer (Synthesis of Polymer B-1)
Into a four-necked flask with an internal volume of 1 liter, 230 parts by mass of ethyl acetate was charged, this mixed solution was sufficiently deaerated by bubbling with nitrogen gas, and the internal temperature of the mixed solution was raised to 70 ° C. Separately, 80 parts by mass of methoxyethyl acrylate (hereinafter referred to as “MEA”), 15 parts by mass of butyl acrylate (hereinafter referred to as “BA”), 5 parts by mass of 2-hydroxyethyl acrylate (hereinafter referred to as “HEA”) Polymerization was carried out by dropping a mixed solution consisting of 1 part by mass of azobisisobutyronitrile (hereinafter referred to as “AIBN”) from the dropping funnel into the flask over 4 hours. After completion of the dropwise addition, 0.3 part of AIBN was further added and aged at 70 ° C. for 3 hours, and the solid content concentration was adjusted to 30% by mass with ethyl acetate to obtain a polymer B-1 solution. Obtained polymer B-1 consisted of MEA 80 mass%, BA 15 mass%, HEA 5 mass%, and was Mw 500,000, Mn 50,000, and Mw / Mn 10.0.

Synthesis Example 16 (Synthesis of Polymer B-2)
Into a four-necked flask with an internal volume of 1 liter, 230 parts by mass of ethyl acetate was charged, this mixed solution was sufficiently deaerated by bubbling with nitrogen gas, and the internal temperature of the mixed solution was raised to 70 ° C. Separately, polymerization was performed by dropping a mixed liquid consisting of 95 parts by mass of BA, 5 parts by mass of HEA, and 1 part by mass of AIBN into the flask from a dropping funnel over 4 hours. After completion of the dropwise addition, 0.3 part of AIBN was further added and aged at 70 ° C. for 3 hours, and the solid content concentration was adjusted to 30% by mass with ethyl acetate to obtain a polymer B-2 solution. The obtained polymer B-2 was composed of 95% by mass of BA and 5% by mass of HEA, and had Mw of 500,000, Mn of 50,000, and Mw / Mn of 10.0.

3. Reference Example 1 for Production and Evaluation of Adhesive Composition
The polymer (A-1) obtained in Synthesis Example 1 was dissolved in ethyl acetate to prepare a polymer (A-1) solution having a solid content concentration of 30% by mass. 10 parts by mass of the polymer (A-1) solution, 100 parts by mass of the polymer B-1 solution, and 0.71 part by mass of Coronate L45 (manufactured by Nippon Polyurethane Industry Co., Ltd.) as a crosslinking agent are mixed to prepare a pressure-sensitive adhesive composition. did.

  This pressure-sensitive adhesive composition was coated on a polyethylene terephthalate (hereinafter referred to as PET) film having a thickness of 38 μm and subjected to heavy release treatment so that the thickness after drying was 50 μm. By drying the pressure-sensitive adhesive composition at 80 ° C. for 4 minutes, ethyl acetate was removed and a crosslinking reaction was performed, and a 38 μm-thick lightly-peeled PET film was bonded, and allowed to stand at 40 ° C. for 5 days. An adhesive sheet with a double-sided separator was obtained.

  About the obtained adhesive sheet, the gel fraction, the compatibility of the acrylic adhesive polymer and the tackifier, and the adhesive strength to polycarbonate and glass were measured by the following methods. The obtained results are shown in Table 2.

<Gel fraction> The 0.2g adhesive was peeled off from the adhesive sheet with a separator, and the initial weight of the adhesive was weighed. The adhesive is immersed in 50 g of ethyl acetate and allowed to stand at room temperature for 16 hours. Thereafter, the mixture was filtered through a 200 mesh wire mesh, and the residue remaining on the mesh was dried at 80 ° C. for 3 hours and weighed. The gel fraction was calculated from the initial weight and the remaining weight.

<Compatibility of acrylic tacky polymer and tackifier> Ten parts by mass and 1 part by mass of a tacky acrylic resin and a tackifier, each having a solid content adjusted to 30% by mass with ethyl acetate, were mixed into the release paper. The solution was dropped and allowed to stand at 80 ° C. for 15 hours to remove ethyl acetate. The dried mixture was sandwiched between glass plates in which 300 μm aluminum films were set at four corners, and allowed to stand at 23 ° C. and 50% RH for 1 day, and the compatibility was evaluated from haze measurement.

<Adhesive strength to polycarbonate and glass> A sample obtained by cutting a pressure-sensitive adhesive sheet into a width of 25 mm is attached to a polycarbonate plate or a glass plate, and JIS Z-0237 “pressure-sensitive adhesive tape / pressure-sensitive adhesive sheet under conditions of 23 ° C. and 50% RH. According to the “Test method”, the 180-degree peel strength of the pressure-sensitive adhesive sheet was measured and used as the adhesive strength. The tensile speed is 300 mm / min. Conditions.

Examples 2-9, Reference Examples 1-2, and Comparative Examples 1-7
In Example 1, the types and ratios of the acrylic pressure-sensitive adhesive polymer and tackifier were changed as shown in Tables 2 and 3 to obtain pressure-sensitive adhesive compositions, and the same measurements as in Example 1 were performed. The results are shown in Tables 2 and 3.

Details of the compounds used in Table 1 are shown below.
ACMO: acryloylmorpholine AAm: acrylamide DMA: dimethylaminoethyl methacrylate MMA: methyl methacrylate St: styrene IBXMA: isobornyl methacrylate BMA: butyl methacrylate

  Examples 1 to 9 using the pressure-sensitive adhesive composition containing the tackifier of the present invention showed high adhesion strength to various adherends together with good transparency. Especially the adhesive strength with respect to glass improved greatly with respect to the comparative example 1 which does not use the below-mentioned tackifier.

On the other hand, Comparative Examples 1 and 2 are examples using a pressure-sensitive adhesive composition that does not contain a tackifier, and the adhesion strength to various adherends, particularly glass, was insufficient. Comparative Examples 3 and 4 are examples in which a vinyl polymer containing no amide group and / or amino group was used as a tackifier, but similarly sufficient adhesive strength was not obtained.
Comparative Example 5 is an example where Mn of the tackifier is outside the range defined by the present invention, but the compatibility with the adhesive polymer is not sufficient, and the transparency of the obtained adhesive layer is insufficient. there were.
Comparative Example 6 and Comparative Example 7 are examples in which the Tg of the tackifier or the amount of the amide group-containing vinyl monomer as a structural unit is outside the range defined by the present invention. It did not give sufficient adhesive strength to the body.

The pressure-sensitive adhesive composition of the present invention can be suitably used for various general pressure-sensitive processed products such as pressure-sensitive adhesive films, pressure-sensitive adhesive sheets, pressure-sensitive adhesive tapes and labels. Specific examples of the adhesive processed product include an adhesive sheet, an adhesive film, an adhesive tape, a pressure sensitive tape, a surface protective film, a surface protective tape, a masking tape, an electrical insulating tape, and a laminate.
In addition to the above, the pressure-sensitive adhesive composition of the present invention is excellent in transparency and has high adhesive strength to various adherends including glass, so that a touch panel, a liquid crystal display device, and an organic EL display device are used. It is also suitable for bonding displays such as plasma display panels and various optical films used in these displays.

Claims (5)

A pressure-sensitive adhesive composition containing a tackifier containing a vinyl polymer and an acrylic pressure-sensitive adhesive polymer,
The vinyl polymer contains a vinyl monomer having an amide group and / or an amino group in a range of more than 10% by mass and 90% by mass or less in all the structural units, and a glass transition temperature (Tg) of 40 to 40%. 150 ° C. and a number average molecular weight of 500 to 10,000,
The acrylic adhesive polymer contains methoxyethyl acrylate as a constituent monomer.
Adhesive composition.   The pressure-sensitive adhesive composition according to claim 1, wherein the vinyl polymer excludes those containing cyclohexyl methacrylate as a constituent monomer.   The vinyl monomer having an amide group and / or amino group is selected from (meth) acryloylmorpholine, (meth) acrylamide, dimethylaminomethyl (meth) acrylate and dimethylaminoethyl (meth) acrylate. It is a seed | species or 2 or more types of vinyl monomers, The adhesive composition of Claim 1 or 2 characterized by the above-mentioned.   The pressure-sensitive adhesive composition according to claim 1, wherein 5 to 60 parts by weight of the tackifier is contained with respect to 100 parts by weight of the acrylic pressure-sensitive adhesive polymer.   A pressure-sensitive adhesive processed product using the pressure-sensitive adhesive composition according to claim 1.