JPWO2016080439A1 - Active energy ray-curable composition, active energy ray-curable pressure-sensitive adhesive composition, pressure-sensitive adhesive and pressure-sensitive adhesive sheet, and novel urethane (meth) acrylate - Google Patents

Abstract

An object of the present invention is to provide an active energy ray-curable composition containing urethane (meth) acrylate having a low dielectric constant and excellent compatibility. The present invention contains a urethane (meth) acrylate (A) which is a reaction product of a polyester-based polyol (a1), a polyisocyanate (a2), and a hydroxyl group-containing (meth) acrylate (a3). The present invention relates to an active energy ray-curable composition having a dielectric constant of A) of 7.0 or less.

Description

The present invention relates to an active energy ray-curable adhesive composition, an active energy ray-curable adhesive composition containing the same, and an adhesive and an adhesive sheet using the active energy ray-curable adhesive composition, More specifically, the active energy ray-curable composition contains urethane (meth) acrylate having a low dielectric constant and excellent compatibility.
The present invention also relates to a novel urethane (meth) acrylate.

  There are various types of adhesives, such as strong adhesives for the purpose of firmly bonding adherends for a long period of time, and peel-off type adhesives that are supposed to be peeled off from adherends after being attached. There are types, and the most suitable adhesive is designed and used for each field.

  Conventionally, as a pressure sensitive adhesive for display members, electronic members, and optical materials, for example, it contains urethane (meth) acrylate obtained by reacting polyol, polyisocyanate, and hydroxyl group-containing (meth) acrylate, and is irradiated with active energy rays. A pressure-sensitive adhesive cured by the above is known. As the polyol, a polyester polyol obtained by condensing a polyvalent carboxylic acid and a polyhydric alcohol, and among them, those using adipic acid as the carboxylic acid are well known (for example, see Patent Document 1).

  In recent years, especially in optical member applications, particularly in touch panel applications, in addition to adhesiveness and moisture and heat resistance, in order to suppress malfunction of the touch panel caused by noise generated from the display member and other peripheral members, the dielectric constant is reduced. There is a need for low adhesives.

  For example, an ultraviolet curable adhesive resin composition containing urethane (meth) acrylate obtained by reacting hydrogenated polybutadiene polyol, polyisocyanate, and hydroxyl group-containing (meth) acrylate as an adhesive having a low dielectric constant is disclosed. (For example, refer to Patent Document 2).

Japanese Unexamined Patent Publication No. 2011-162770 Japanese Unexamined Patent Publication No. 2002-309185

  However, the urethane (meth) acrylate obtained by reacting a polyester polyol using adipic acid, polyisocyanate, and a hydroxyl group-containing (meth) acrylate disclosed in Patent Document 1 has a dielectric constant of usually about 8.0. However, when applied to an optical member, the required performance was not satisfied in terms of suppressing malfunction of the touch panel.

  The urethane (meth) acrylate obtained by reacting the hydrogenated polybutadiene polyol, polyisocyanate, and hydroxyl group-containing (meth) acrylate described in Patent Document 2 has a low dielectric constant of about 3.0, but it is a hydrogenated polybutadiene polyol. Since urethane (meth) acrylate itself has low polarity and is not sufficiently compatible with other monomers and resins, there are problems such as low freedom of material selection and difficulty in handling.

  Therefore, in the present invention, an object of the present invention is to provide an active energy ray-curable composition containing urethane (meth) acrylate having a low dielectric constant and excellent compatibility under such a background. is there. Furthermore, it aims at providing the active energy ray curable adhesive composition containing this active energy ray curable composition, the adhesive using the same, an adhesive sheet, and a novel urethane (meth) acrylate.

  However, as a result of intensive studies in view of such circumstances, the present inventors have found that the urethane (meth) acrylate is an active energy ray-curable composition containing a urethane (meth) acrylate obtained by reacting a polyester polyol. The inventors found that an adhesive having a low dielectric constant and excellent compatibility can be obtained by setting the dielectric constant to a specific value or less, and the present invention has been completed.

That is, the gist of the present invention is as follows.
[1] A urethane (meth) acrylate (A) that is a reaction product of a polyester-based polyol (a1), a polyisocyanate (a2), and a hydroxyl group-containing (meth) acrylate (a3). An active energy ray-curable composition having a dielectric constant of A) of 7.0 or less.
[2] The active energy ray-curable composition according to [1], wherein the oxygen atom content X in the repeating structural unit of the polyester-based polyol (a1) is 0.35 or less. However, the content X is a value represented by the following formula (1).
X = 16c / (12a + b + 16c) (1)
a: Number of carbon atoms in the repeating structural unit of the polyester-based polyol (a1) b: Number of hydrogen atoms in the repeating structural unit of the polyester-based polyol (a1) c: In the repeating structural unit of the polyester-based polyol (a1) Number of oxygen atoms [3] The polyester polyol (a1) is a polycondensate of a polyvalent carboxylic acid component containing a polyvalent carboxylic acid having an alkylene group having 5 to 20 carbon atoms and a polyhydric alcohol component. The active energy ray-curable composition according to [1] or [2].
[4] The active energy ray-curable composition according to any one of [1] to [3], wherein the polyester-based polyol (a1) has a number average molecular weight of 500 to 12,000.
[5] The active energy ray-curable composition according to any one of [1] to [4], wherein the urethane (meth) acrylate (A) has a weight average molecular weight of 1,000 to 100,000.
[6] The active energy ray curing according to any one of [1] to [5], further including an ethylenically unsaturated monomer (B) (excluding the urethane (meth) acrylate (A)). Sex composition.
[7] An active energy ray-curable pressure-sensitive adhesive composition containing the active energy ray-curable composition according to any one of [1] to [6].
[8] A pressure-sensitive adhesive obtained by curing the active energy ray-curable pressure-sensitive adhesive composition according to [7].
[9] A pressure-sensitive adhesive sheet in which the pressure-sensitive adhesive according to [8] is laminated on a base material sheet.
[10] Polyester polyol (a1), polyisocyanate (a2) and hydroxyl group which are polycondensates of a polyhydric carboxylic acid component containing a polyhydric carboxylic acid having an alkylene group having 5 to 20 carbon atoms and a polyhydric alcohol component Urethane (meth) acrylate which is a reaction product of containing (meth) acrylate (a3).

  According to the active energy ray-curable composition of the present invention, a pressure-sensitive adhesive composition having a low dielectric constant and excellent compatibility can be obtained, and the pressure-sensitive adhesive cured is useful as a pressure-sensitive adhesive for optical members. Especially, it is suitably used for touch panel applications and the like.

Hereinafter, the present invention will be described in detail.
In the present invention, (meth) acrylic acid is acrylic acid and / or methacrylic acid, (meth) acryl is acrylic and / or methacrylic, (meth) acryloyl is acryloyl and / or methacryloyl, ) Acrylate means acrylate and / or methacrylate, respectively. The acrylic resin is a resin obtained by polymerizing at least one (meth) acrylate monomer alone, or a resin obtained by polymerizing a polymerization component containing at least one (meth) acrylate monomer. is there.
Further, in the present specification, “to” indicating a numerical range is used in a sense including numerical values described before and after the numerical value as a lower limit value and an upper limit value.

  The active energy ray-curable composition of the present invention comprises a urethane (meth) acrylate (a reaction product obtained by reacting a polyester polyol (a1), a polyisocyanate (a2), and a hydroxyl group-containing (meth) acrylate (a3) ( An active energy ray-curable composition containing A) and having a dielectric constant of the urethane (meth) acrylate (A) of 7.0 or less.

Here, the dielectric constant is a value representing the degree of polarization of a substance when an electric field is applied.
In the present invention, the dielectric constant of urethane (meth) acrylate is the active energy ray curability in which 4 parts by weight of 1-hydroxy-cyclohexyl-phenyl-ketone and a solvent are mixed with 100 parts by weight of urethane (meth) acrylate. This is a value obtained by measuring the dielectric constant of a cured film obtained by curing the composition, and is specifically measured by the following method.

(Measuring method)
A film thickness after curing an active energy ray-curable composition in which 4 parts by weight of 1-hydroxy-cyclohexyl-phenyl-ketone as a photopolymerization initiator and a solvent are blended with 100 parts by weight of urethane (meth) acrylate. Is applied to an untreated polyethylene terephthalate (PET) film (thickness 50 μm) using an applicator so that the thickness of the solvent becomes 150 μm, and the solvent is volatilized by placing it in a dryer at 60 ° C. for 10 minutes. Then, the active energy ray-curable composition surface is laminated from above with an untreated polyethylene terephthalate (PET) film (thickness 50 μm), and is applied to a tabletop UV irradiation device (“Conveyor type tabletop irradiation device” manufactured by Eye Graphics). 80W / cm (high pressure mercury lamp) × 18 cmH × 2.04 m / min × 3 Pass (integrated irradiation amount 2,400 mJ / cm ² ) Cut out to 7 cm × 7 cm to obtain a test piece for dielectric constant measurement.
Using the HP4284A Precision LCR meter (manufactured by Agilent), the dielectric constant measurement test piece is measured by placing an electric field at a frequency of 1 MHz by sandwiching the test piece between the electrodes and measuring the change in capacitance between the electrodes. The dielectric constant of the active energy ray curable composition is calculated.

  The urethane (meth) acrylate (A) used in the present invention is a reaction product obtained by reacting a polyester polyol (a1), a polyisocyanate (a2), and a hydroxyl group-containing (meth) acrylate (a3).

  Examples of the polyester-based polyol (a1) in the present invention include a condensation polymer (polycondensate) of a polyhydric alcohol component and a polyvalent carboxylic acid component, a ring-opening polymer of a cyclic ester (lactone) component, and a polyvalent polyol. The reaction material by three types of components, such as an alcohol component, a polyhydric carboxylic acid component, and a cyclic ester component, is mentioned.

Examples of the polyhydric alcohol component include ethylene glycol, diethylene glycol, propylene glycol, dipropylene glycol, trimethylene glycol, 1,4-tetramethylene diol, 1,3-tetramethylene diol, 2-methyl-1,3- Trimethylene diol, 1,5-pentamethylene diol, neopentyl glycol, 1,6-hexamethylene diol, 3-methyl-1,5-pentamethylene diol, 2,4-diethyl-1,5-pentamethylene diol, Dihydric alcohols such as 1,9-nonanediol, cyclohexanediols (such as 1,4-cyclohexanediol) and bisphenols (such as bisphenol A), trihydric alcohols such as glycerin, trimethylolpropane and trimethylolethane, sugars Like alcohol compound (such as xylitol or sorbitol). Among these, a dihydric alcohol is preferable in terms of excellent versatility, ethylene glycol, diethylene glycol, propylene glycol, dipropylene glycol, trimethylene glycol, 1,4-tetramethylene diol, 2-methyl-1,3-trimethylene. Diol and neopentyl glycol are particularly preferred.
These may be used alone or in combination of two or more.

Examples of the polyvalent carboxylic acid component include aliphatic dicarboxylic acids such as malonic acid, maleic acid, fumaric acid, succinic acid, glutaric acid, adipic acid, suberic acid, azelaic acid, sebacic acid, and dodecanedioic acid; Examples include alicyclic dicarboxylic acids such as 4-cyclohexanedicarboxylic acid; aromatic dicarboxylic acids such as terephthalic acid, isophthalic acid, orthophthalic acid, 2,6-naphthalenedicarboxylic acid, paraphenylenedicarboxylic acid, trimellitic acid, and the like. Among these, aliphatic dicarboxylic acids are preferable in terms of less yellowing, and succinic acid, adipic acid, and sebacic acid are particularly preferable.
These may be used alone or in combination of two or more.

  Examples of the cyclic ester component include propiolactone, β-methyl-δ-valerolactone, and ε-caprolactone.

In the present invention, from the viewpoint of low dielectric properties, the polyester polyol (a1) preferably has an oxygen atom content X in the repeating structural unit of the polyester polyol (a1) of 0.35 or less. However, the content X is a value represented by the following formula (1).
X = 16c / (12a + b + 16c) (1)
a: Number of carbon atoms in the repeating structural unit of the polyester-based polyol (a1) b: Number of hydrogen atoms in the repeating structural unit of the polyester-based polyol (a1) c: In the repeating structural unit of the polyester-based polyol (a1) Number of oxygen atoms

  For example, when the polyester polyol (a1) is a copolymer of ethylene glycol and adipic acid, the repeating structural unit is represented by the following structural formula. In the structural formula, n represents the number of repeating structural units.

  In this case, since a = 8, b = 12, and c = 4 in the above formula (1), the oxygen atom content X in the repeating structural unit represented by the above formula (1) is X = 0.37. .

From the viewpoint of low dielectric constant, the polyvalent carboxylic acid component constituting the polyester polyol (a1) may contain a polyvalent carboxylic acid having an alkylene group having 5 to 20 carbon atoms. Further, it is preferable to contain a polyvalent carboxylic acid having an alkylene group having 6 to 18 carbon atoms, particularly 7 to 16 carbon atoms. The polyester-based polyol (a1) is more preferably a polycondensate of a polyvalent carboxylic acid component containing a polyvalent carboxylic acid having an alkylene group having 5 to 20 carbon atoms and a polyhydric alcohol component.
When the number of carbon atoms of the alkylene group of the polyvalent carboxylic acid is too small, the dielectric constant tends to increase. When the number of carbon atoms is too large, the crystallinity increases and the handling tends to be difficult.
Specific examples of the polyvalent carboxylic acid having an alkylene group having 5 to 20 carbon atoms include pimelic acid, suberic acid, azelaic acid, sebacic acid, dodecanoic acid, eicosanoic acid, and isoeicosanoic acid.

In the case of using a polyvalent carboxylic acid having an alkylene group having 5 to 20 carbon atoms, it is preferably contained in an amount of 10 to 100 mol% based on the entire polyvalent carboxylic acid component, from the viewpoint of low dielectric constant, More preferably, it is 20-100 mol%, Most preferably, it is 25-100 mol%, Most preferably, it is 30-100 mol%.
If the content ratio of the polyvalent carboxylic acid having an alkylene group having 5 to 20 carbon atoms relative to the entire polyvalent carboxylic acid component is too small, the dielectric constant tends to increase.

  Further, the number of hydroxyl groups contained in the polyester polyol (a1) is preferably 2 to 5, particularly preferably 2 to 3, and more preferably 2 per molecule. If the number of hydroxyl groups is too large, gelation tends to occur during the reaction.

The number average molecular weight of the polyester polyol (a1) is preferably 500 to 12,000, more preferably 600 to 10,000, and particularly preferably 700 to 8,000.
If the number average molecular weight is too large, the viscosity tends to increase and the workability tends to decrease, and if it is too small, sufficient tackiness tends to be difficult to obtain.

  In addition, said number average molecular weight is the value calculated | required by the following formula.

  The number of functional groups (F) in the formula represents the number of hydroxyl groups contained in one molecule.

  As a hydroxyl value of the said polyester-type polyol (a1), it is preferable that it is 10-400 mgKOH / g, Most preferably, it is 20-300 mgKOH / g, More preferably, it is 30-250 mgKOH / g. If the hydroxyl value is too high, the urethane (meth) acrylate tends to have a low molecular weight and the adhesiveness tends to decrease, and if it is too low, the viscosity tends to increase and the workability tends to decrease.

  The hydroxyl value can be measured based on JIS K 0070-1992.

  Examples of the polyisocyanate (a2) include aromatic polyisocyanates such as tolylene diisocyanate, diphenylmethane diisocyanate, polyphenylmethane polyisocyanate, modified diphenylmethane diisocyanate, xylylene diisocyanate, tetramethylxylylene diisocyanate, phenylene diisocyanate, and naphthalene diisocyanate. , Pentamethylene diisocyanate, hexamethylene diisocyanate, trimethylhexamethylene diisocyanate, lysine diisocyanate, lysine triisocyanate and other aliphatic polyisocyanates, hydrogenated diphenylmethane diisocyanate, hydrogenated xylylene diisocyanate, isophorone diisocyanate, norbornene diisocyanate, 1,3 -Bi (Isocyanatomethyl) cyclohexane, alicyclic polyisocyanates, or trimers compound or multimeric compounds of these polyisocyanates, allophanate type polyisocyanate, buret type polyisocyanate, water dispersible polyisocyanate, and the like.

Of these, diisocyanates are preferred from the viewpoint of excellent reaction stability. In particular, aliphatic diisocyanates such as pentamethylene diisocyanate, hexamethylene diisocyanate, trimethylhexamethylene diisocyanate, and lysine diisocyanate, hydrogenated diphenylmethane diisocyanate, hydrogenated xylylene. Cycloaliphatic diisocyanates such as diisocyanate, isophorone diisocyanate, norbornene diisocyanate, 1,3-bis (isocyanatomethyl) cyclohexane are preferably used, and more preferably hydrogenated xylylene diisocyanate in terms of excellent reactivity and versatility. Isophorone diisocyanate is used.
Moreover, the said polyisocyanate can be used individually by 1 type, or can be used in combination of 2 or more type.

  Examples of the hydroxyl group-containing (meth) acrylate (a3) include 2-hydroxyethyl (meth) acrylate, 2-hydroxypropyl (meth) acrylate, 2-hydroxybutyl (meth) acrylate, and 4-hydroxybutyl (meth) acrylate. , Hydroxyalkyl (meth) acrylates such as 6-hydroxyhexyl (meth) acrylate having 2 to 20 carbon atoms (preferably 2 to 18), 2-hydroxyethylacryloyl phosphate, 2- (meth) acryloyl Roxyethyl-2-hydroxypropyl phthalate, caprolactone-modified 2-hydroxyethyl (meth) acrylate, dipropylene glycol (meth) acrylate, fatty acid-modified glycidyl (meth) acrylate, polyethylene glycol mono (me ) Acrylate, polypropylene glycol mono (meth) acrylate, 2-hydroxy-3- (meth) acryloyloxypropyl (meth) acrylate, and other (meth) acrylates containing one ethylenically unsaturated group; glycerin di (meta) ) (Meth) acrylates containing two ethylenically unsaturated groups such as acrylate, 2-hydroxy-3-acryloyl-oxypropyl methacrylate; pentaerythritol tri (meth) acrylate, caprolactone-modified pentaerythritol tri (meth) acrylate, ethylene Oxide-modified pentaerythritol tri (meth) acrylate, dipentaerythritol penta (meth) acrylate, caprolactone-modified dipentaerythritol penta (meth) acrylate, ethylene oxide The modified dipentaerythritol penta (meth) acrylate ethylenically unsaturated groups such as containing three or more (meth) acrylate. The said hydroxyl-containing (meth) acrylate (a3) can be used individually by 1 type, or can be used in combination of 2 or more type.

  Among these, a hydroxyl group-containing (meth) acrylate having one ethylenically unsaturated group is preferable in terms of excellent flexibility of the pressure-sensitive adhesive layer, and more preferably 2-hydroxyethyl (meth) acrylate and 2-hydroxypropyl. Hydroxyalkyl (meth) acrylates such as (meth) acrylate, 2-hydroxybutyl (meth) acrylate, 4-hydroxybutyl (meth) acrylate, 6-hydroxyhexyl (meth) acrylate, and in particular 2-hydroxyethyl (meta) ) Use of acrylate or 4-hydroxybutyl (meth) acrylate is preferable in terms of excellent reactivity and versatility.

In the present invention, the urethane (meth) acrylate (A) can be produced as follows.
For example, (1) polyester-based polyol (a1), polyisocyanate (a2), hydroxyl group-containing (meth) acrylate (a3) are charged into a reactor or reacted separately, (2) polyester-based polyol (a1) ) And polyisocyanate (a2) in advance, a reaction product obtained by reacting a hydroxyl group-containing (meth) acrylate (a3) with a reaction product obtained in advance, the stability of the reaction and reduction of by-products In view of the above, the method (2) is preferable.

  The urethane (meth) acrylate (A) is a polyester polyol (a1) which is a polycondensate of a polyhydric carboxylic acid component containing a polyhydric carboxylic acid having an alkylene group having 5 to 20 carbon atoms and a polyhydric alcohol component. ), A polyisocyanate (a2) and a reaction product of a hydroxyl group-containing (meth) acrylate (a3), and the reaction product urethane (meth) acrylate is a novel compound regardless of its dielectric constant. .

A method of reacting a hydroxyl group-containing (meth) acrylate (a3) with a reaction product obtained by reacting a polyester-based polyol (a1) and a polyisocyanate (a2) in advance in producing the urethane (meth) acrylate (A). Will be described.
A known reaction means can be used for the reaction of the polyester polyol (a1) and the polyisocyanate (a2). At that time, for example, the molar ratio of the isocyanate group in the polyisocyanate (a2) to the hydroxyl group in the polyester polyol (a1) is usually about 2n: (2n-2) (n is an integer of 2 or more). A terminal isocyanate group-containing urethane (meth) acrylate having an isocyanate group remaining can be obtained, and after obtaining the compound, an addition reaction with the hydroxyl group-containing (meth) acrylate (a3) is made possible.

  For the addition reaction of the reaction product obtained by reacting the polyester polyol (a1) and the polyisocyanate (a2) in advance with the hydroxyl group-containing (meth) acrylate (a3), a known reaction means may be used. it can.

  The reaction molar ratio of the reaction product to the hydroxyl group-containing (meth) acrylate (a3) is, for example, that the reaction product has two isocyanate groups and the hydroxyl group-containing (meth) acrylate (a3) has one hydroxyl group. In some cases, the reaction product: hydroxyl group-containing (meth) acrylate (a3) is about 1: 2, the reaction product has three isocyanate groups, and the hydroxyl group-containing (meth) acrylate (a3) has 1 hydroxyl group. In the case of individual, the reaction product: hydroxyl group-containing (meth) acrylate (a3) is about 1: 3.

  In the addition reaction between the reaction product and the hydroxyl group-containing (meth) acrylate (a3), the reaction is terminated when the residual isocyanate group content in the reaction system is 0.3% by weight or less. A (meth) acrylate (A) is obtained.

  In the reaction between the polyester-based polyol (a1) and the polyisocyanate (a2) and the reaction product with the hydroxyl group-containing (meth) acrylate (a3), it is also preferable to use a catalyst for the purpose of promoting the reaction. . Examples of such catalysts include dibutyltin dilaurate, dibutyltin diacetate, trimethyltin hydroxide, tetra-n-butyltin, bisacetylacetonate zinc, zirconium tris (acetylacetonate) ethylacetoacetate, zirconium tetraacetylacetonate. Organometallic compounds such as tin octenoate, zinc hexanoate, zinc octenoate, zinc stearate, zirconium 2-ethylhexanoate, cobalt naphthenate, stannous chloride, stannic chloride, potassium acetate and the like, Triethylamine, triethylenediamine, benzyldiethylamine, 1,4-diazabicyclo [2,2,2] octane, 1,8-diazabicyclo [5,4,0] undecene, N, N, N ′, N′-tetramethyl-1 , 3-butanediamine, N-me In addition to amine-based catalysts such as lumorpholine and N-ethylmorpholine, bismuth nitrate, bismuth bromide, bismuth iodide, bismuth sulfide, etc., organic bismuth compounds such as dibutyl bismuth dilaurate and dioctyl bismuth dilaurate, and bismuth 2-ethylhexanoate Bismuth naphthenate, bismuth isodecanoate, bismuth neodecanoate, bismuth laurate, bismuth maleate, bismuth stearate, bismuth oleate, bismuth linoleate, bismuth acetate, bismuth bisneodecano Bismuth-based catalysts such as organic acid bismuth salts such as bismuthate, bismuth disalicylate, and digallic acid bismuth, among others, dibutyltin dilaurate and 1,8-diazabicyclo [5,4,0] undecene are preferred. is there. These may be used alone or in combination of two or more.

  In the reaction between the polyester polyol (a1) and the polyisocyanate (a2), and further in the reaction between the reaction product and the hydroxyl group-containing (meth) acrylate (a3), it reacts with an isocyanate group as necessary. Organic solvents having no functional group, for example, esters such as ethyl acetate and butyl acetate, ketones such as methyl ethyl ketone and methyl isobutyl ketone, organic solvents such as aromatics such as toluene and xylene, and ethylenically unsaturated monomers ( For example, you may use the compound which is mentioned to the below-mentioned ethylenically unsaturated monomer (B).

  Moreover, reaction temperature is 30-90 degreeC normally, Preferably it is 40-80 degreeC, and reaction time is 2 to 10 hours normally, Preferably it is 3 to 8 hours.

The urethane (meth) acrylate (A) of the present invention thus obtained has a dielectric constant of 7.0 or less, and is preferably 6.5 or less, more preferably 6.0 or less, from the viewpoint of suppressing malfunction of the touch panel. is there. The lower limit of the dielectric constant is usually 1.0.
If the dielectric constant is too high, the capacitance between the electrodes mounted on the touch panel tends to increase, which tends to cause a malfunction. If the dielectric constant is too low, the capacitance decreases, and the detection sensitivity tends to decrease.

  The weight average molecular weight of the urethane (meth) acrylate (A) of the present invention is preferably 1,000 to 100,000, particularly preferably 5,000 to 90,000, and more preferably 10,000 to 80,000. 000. If the weight average molecular weight is too small, the adhesive strength tends to decrease, and if it is too large, the viscosity becomes too high and coating tends to be difficult.

In addition, said weight average molecular weight is a weight average molecular weight by standard polystyrene molecular weight conversion, column: Shodex GPC KF-806L (exclusion) in a high performance liquid chromatography (Showa Denko Co., Ltd. make, "Shodex GPC system-11 type | mold"). Limit molecular weight: 2 × 10 ⁷ , separation range: 100 to 2 × 10 ⁷ , theoretical plate number: 10,000 plate / piece, filler material: styrene-divinylbenzene copolymer, filler particle size: 10 μm) It is a value measured by using a series.

Moreover, about the viscosity of the urethane (meth) acrylate (A) of this invention, it is preferable that it is a viscosity in 60 degreeC, and is 1,000-1,000,000 mPa * s, Most preferably, it is 2,000-900, 000 mPa · s, more preferably 3,000 to 800,000 mPa · s. If the viscosity is too high, handling tends to be difficult, and if it is too low, control of the film thickness tends to be difficult during coating.
In addition, the measuring method of a viscosity is based on an E-type viscometer.

In addition to the urethane (meth) acrylate (A), the active energy ray-curable composition of the present invention further contains an ethylenically unsaturated monomer (B) (excluding the urethane (meth) acrylate (A)). It is preferable to contain.
Examples of the ethylenically unsaturated monomer (B) used in the present invention include a monofunctional monomer, a bifunctional monomer, and a trifunctional or higher monomer.

  Examples of such monofunctional monomers include styrene monomers such as styrene, vinyl toluene, chlorostyrene, α-methylstyrene, methyl (meth) acrylate, ethyl (meth) acrylate, acrylonitrile, 2-methoxyethyl (meth) acrylate, 2-hydroxyethyl (meth) acrylate, 2-hydroxypropyl (meth) acrylate, 2-hydroxybutyl (meth) acrylate, 4-hydroxybutyl (meth) acrylate, phenoxyethyl (meth) acrylate, 2-phenoxy-2-hydroxy Propyl (meth) acrylate, 2-hydroxy-3-phenoxypropyl (meth) acrylate, 3-chloro-2-hydroxypropyl (meth) acrylate, glycerin mono (meth) acrylate, glycidyl (Meth) acrylate, lauryl (meth) acrylate, cyclohexyl (meth) acrylate, isobornyl (meth) acrylate, tricyclodecanyl (meth) acrylate, dicyclopentenyl (meth) acrylate, dicyclopentenyloxyethyl (meth) acrylate, Dicyclopentanyl (meth) acrylate, (2-methyl-2-ethyl-1,3-dioxolan-4-yl) -methyl (meth) acrylate, cyclohexanespiro-2- (1,3-dioxolan-4-yl ) -Methyl (meth) acrylate, 3-ethyl-3-oxetanylmethyl (meth) acrylate, γ-butyrolactone (meth) acrylate, n-butyl (meth) acrylate, hexyl (meth) acrylate, heptyl (meth) acrylate, octi (Meth) acrylate, nonyl (meth) acrylate, decyl (meth) acrylate, isodecyl (meth) acrylate, dodecyl (meth) acrylate, n-stearyl (meth) acrylate, benzyl (meth) acrylate, phenol ethylene oxide modified (n = 2) Phthal such as (meth) acrylate, nonylphenol propylene oxide modified (n = 2.5) (meth) acrylate, 2- (meth) acryloyloxyethyl acid phosphate, 2- (meth) acryloyloxy-2-hydroxypropyl phthalate Acid derivatives half (meth) acrylate, furfuryl (meth) acrylate, tetrahydrofurfuryl (meth) acrylate, carbitol (meth) acrylate, benzyl (meth) acrylate, butoxy (Meth) acrylate monomers such as chill (meth) acrylate, allyl (meth) acrylate, (meth) acryloylmorpholine, polyoxyethylene secondary alkyl ether acrylate, 2-hydroxyethylacrylamide, N-methylol (meth) acrylamide N-vinylpyrrolidone, 2-vinylpyridine, vinyl acetate, and the like.

  Examples of such bifunctional monomers include ethylene glycol di (meth) acrylate, diethylene glycol di (meth) acrylate, tetraethylene glycol di (meth) acrylate, polyethylene glycol di (meth) acrylate, propylene glycol di (meth) acrylate, and di Propylene glycol di (meth) acrylate, polypropylene glycol di (meth) acrylate, butylene glycol di (meth) acrylate, neopentyl glycol di (meth) acrylate, ethylene oxide modified bisphenol A type di (meth) acrylate, propylene oxide modified bisphenol A Type di (meth) acrylate, cyclohexanedimethanol di (meth) acrylate, ethoxylated cyclohexanedimethanol di (me ) Acrylate, dimethylol dicyclopentane di (meth) acrylate, tricyclodecane dimethanol di (meth) acrylate, 1,6-hexanediol di (meth) acrylate, glycerin di (meth) acrylate, pentaerythritol di (meth) Acrylate, ethylene glycol diglycidyl ether di (meth) acrylate, diethylene glycol diglycidyl ether di (meth) acrylate, diglycidyl phthalate di (meth) acrylate, hydroxypivalic acid modified neopentyl glycol di (meth) acrylate, ethylene isocyanurate Examples thereof include oxide-modified diacrylate.

  Examples of the tri- or higher functional monomer include trimethylolpropane tri (meth) acrylate, pentaerythritol tri (meth) acrylate, pentaerythritol tetra (meth) acrylate, dipentaerythritol penta (meth) acrylate, dipentaerythritol hexa ( (Meth) acrylate, tri (meth) acryloyloxyethoxytrimethylolpropane, glycerin polyglycidyl ether poly (meth) acrylate, isocyanuric acid ethylene oxide modified triacrylate, caprolactone modified dipentaerythritol penta (meth) acrylate, caprolactone modified dipentaerythritol hexa (Meth) acrylate, caprolactone-modified pentaerythritol tri (meth) acrylate, capro Kuton modified pentaerythritol tetra (meth) acrylate, ethylene oxide modified dipentaerythritol penta (meth) acrylate, ethylene oxide modified dipentaerythritol hexa (meth) acrylate, ethylene oxide modified pentaerythritol tri (meth) acrylate, ethylene oxide modified pentaerythritol Examples include tetra (meth) acrylate and ethoxylated glycerin triacrylate.

Also, a Michael adduct of acrylic acid or 2-acryloyloxyethyl dicarboxylic acid monoester can be used in combination, and as such a Michael adduct of acrylic acid, acrylic acid dimer, methacrylic acid dimer, acrylic acid trimer, methacrylic acid trimer, An acrylic acid tetramer, a methacrylic acid tetramer, etc. are mentioned.
The 2-acryloyloxyethyl dicarboxylic acid monoester is a carboxylic acid having a specific substituent, such as 2-acryloyloxyethyl succinic acid monoester, 2-methacryloyloxyethyl succinic acid monoester, 2-acryloyloxyethyl. Examples include phthalic acid monoester, 2-methacryloyloxyethyl phthalic acid monoester, 2-acryloyloxyethyl hexahydrophthalic acid monoester, and 2-methacryloyloxyethyl hexahydrophthalic acid monoester. Furthermore, other oligoester acrylates can also be mentioned.

  The content of the ethylenically unsaturated monomer (B) is preferably 5 to 900 parts by weight, particularly preferably 10 to 600 parts by weight, more preferably 100 parts by weight of the urethane (meth) acrylate (A). Is 15 to 400 parts by weight. When the content is too large, the viscosity tends to be low and the adhesive strength tends to decrease. When the content is too small, the viscosity tends to be high and coating properties tend to decrease.

  In the present invention, the active energy ray-curable composition preferably further contains a photopolymerization initiator (C), and the photopolymerization initiator (C) generates radicals by the action of light. If there is no particular limitation. For example, diethoxyacetophenone, 2-hydroxy-2-methyl-1-phenylpropan-1-one, benzyldimethyl ketal, 4- (2-hydroxyethoxy) phenyl- (2-hydroxy-2-propyl) ketone, 1- Hydroxycyclohexyl phenyl ketone, 1- [4- (2-hydroxyethoxy) -phenyl] -2-hydroxy-2-methyl-1-propan-1-one, 2-methyl-2-morpholino (4-thiomethylphenyl) Propan-1-one, 2-benzyl-2-dimethylamino-1- (4-morpholinophenyl) butanone, 2-hydroxy-2-methyl-1- [4- (1-methylvinyl) phenyl] propanone oligomer, etc. Acetophenones; benzoin, benzoin methyl ether, benzoin ethyl ether, Benzoins such as benzoin isopropyl ether and benzoin isobutyl ether; benzophenone, methyl o-benzoylbenzoate, 4-phenylbenzophenone, 4-benzoyl-4'-methyl-diphenyl sulfide, 3,3 ', 4,4'- Tetra (t-butylperoxycarbonyl) benzophenone, 2,4,6-trimethylbenzophenone, 4-benzoyl-N, N-dimethyl-N- [2- (1-oxo-2-propenyloxy) ethyl] benzenemethanami Benzophenones such as nium bromide and (4-benzoylbenzyl) trimethylammonium chloride; 2-isopropylthioxanthone, 4-isopropylthioxanthone, 2,4-diethylthioxanthone, 2,4-dichlorothioxanthone, 1-chloro-4-pro Thioxanthones such as xylthioxanthone, 2- (3-dimethylamino-2-hydroxy) -3,4-dimethyl-9H-thioxanthone-9-one mesochloride; 2,4,6-trimethylbenzoyl-diphenylphosphine oxide, Acyl phosphine oxides such as bis (2,6-dimethoxybenzoyl) -2,4,4-trimethyl-pentylphosphine oxide, bis (2,4,6-trimethylbenzoyl) -phenylphosphine oxide; It is done. In addition, these photoinitiators (C) can be used individually by 1 type, or can use 2 or more types together.

  Further, as an auxiliary of these photopolymerization initiators (C), triethanolamine, triisopropanolamine, 4,4′-dimethylaminobenzophenone (Michler ketone), 4,4′-diethylaminobenzophenone, 2-dimethylaminoethylbenzoic acid Ethyl 4-dimethylaminobenzoate, ethyl 4-dimethylaminobenzoate (n-butoxy), isoamyl 4-dimethylaminobenzoate, 2-ethylhexyl 4-dimethylaminobenzoate, 2,4-diethylthioxanthone, 2 , 4-Diisopropylthioxanthone can also be used in combination. These auxiliaries can be used alone or in combination of two or more.

  About content of this photoinitiator (C), urethane (meth) acrylate (A) (when further containing ethylenically unsaturated monomer (B), urethane (meth) acrylate (A) and ethylenically unsaturated The amount is preferably 1 to 10 parts by weight, particularly preferably 2 to 5 parts by weight, based on 100 parts by weight of the total of the saturated monomers (B). If the content is too small, the curing rate tends to decrease. If the content is too large, the curability does not improve and the economy tends to decrease.

  In addition to urethane (meth) acrylate (A), ethylenically unsaturated monomer (B), photopolymerization initiator (C) and the like, the active energy ray-curable composition of the present invention includes an antioxidant, a flame retardant, Antistatic agents, fillers, leveling agents, stabilizers, reinforcing agents, matting agents and the like can also be blended. Furthermore, as the crosslinking agent, a compound having an action of causing crosslinking by heat, specifically, an epoxy compound, an aziricin compound, a melamine compound, an isocyanate compound, a chelate compound, and the like can be used. A carbodiimide compound can also be used as a hydrolysis inhibitor.

In addition, the active energy ray-curable composition of the present invention is prepared by using alcohol such as methanol, ethanol, propanol, n-butanol, i-butanol for dilution in order to adjust the viscosity at the time of coating, if necessary. , Ketones such as acetone, methyl isobutyl ketone, methyl ethyl ketone, cyclohexanone, cellosolves such as ethyl cellosolve, aromatics such as toluene and xylene, glycol ethers such as propylene glycol monomethyl ether, methyl acetate, ethyl acetate, butyl acetate Diluting solvents such as acetic acid esters, diacetone alcohol, etc. may be used, but since the solvent remains in the coating film and the curing component may volatilize during drying, it contains substantially no solvent. Preferably not.
Note that “substantially free of solvent” is usually 1% by weight or less, preferably 0.5% by weight or less, more preferably 0.1% by weight or less, based on the entire active energy ray-curable composition. Point to.

  The active energy ray-curable composition of the present invention can be used as a coating composition for various substrate films, and can be used as a pressure-sensitive adhesive composition such as bonding of various members and a surface protective sheet. It is particularly useful to use an energy ray-curable pressure-sensitive adhesive composition.

Furthermore, the active energy ray-curable pressure-sensitive adhesive composition of the present invention can also contain a tackifier such as a polythiol compound from the viewpoint of suppressing unreacted components and improving adhesive force.
As the polythiol compound, a compound having 2 to 6 mercapto groups in the molecule is preferable. For example, aliphatic polythiols such as alkanedithiol having about 2 to 20 carbon atoms, aromatic polythiols such as xylylene thiol, alcohols Polythiols in which the halogen atom of the halohydrin adduct is substituted with a mercapto group, polythiols comprising a hydrogen sulfide reaction product of a polyepoxide compound, polyhydric alcohols having 2 to 6 hydroxyl groups in the molecule, thioglycolic acid, β -The polythiols which consist of an esterified product with mercaptopropionic acid or (beta) -mercaptobutanoic acid etc. can be mentioned, Among these, 1 type or 2 types or more can be used.

  When the polythiol compound is contained, the content is urethane (meth) acrylate (A) (and further contains ethylenically unsaturated monomer (B), urethane (meth) acrylate (A) and ethylenically unsaturated monomer. The total of (B)) is preferably 10 parts by weight or less, particularly preferably 0.01 to 5 parts by weight with respect to 100 parts by weight.

The active energy ray-curable pressure-sensitive adhesive composition of the present invention is preferably a cured pressure-sensitive adhesive. Specifically, it is usually applied to a base sheet and the like and is often used as a pressure-sensitive adhesive sheet. After coating on a base sheet or the like, it is crosslinked by irradiation with active energy rays to become a pressure-sensitive adhesive. Is expressed.
The pressure-sensitive adhesive sheet is meant to include a pressure-sensitive adhesive film and a pressure-sensitive adhesive tape unless otherwise specified, and is characterized in that a pressure-sensitive adhesive obtained by curing the active energy ray-curable pressure-sensitive adhesive composition of the present invention is laminated. To do.

  Moreover, in this invention, a separator can be laminated | stacked on the surface of an adhesive for the purpose of protecting an adhesive from contamination until an adhesive sheet is bonded together to a to-be-adhered body (member).

  Examples of the base sheet include polyester resins such as polyethylene terephthalate and polybutylene terephthalate, polyolefin resins such as polyethylene, polypropylene, and ethylene-propylene copolymer, polycarbonate resins, polyurethane resins, acrylic resins, and polystyrene. Examples thereof include resin sheets such as resin, ethylene-vinyl acetate copolymer, polyvinyl chloride, polybutene, polyester, polymethylpentene, acrylonitrile butadiene styrene copolymer (ABS), and glass plates. Various substrate sheets may be subjected to surface treatment such as anchor layer, corona treatment, plasma treatment, and the like.

  As said separator, what carried out mold release processing of base materials, such as the resin sheet illustrated above as a base material sheet, paper, cloth, and a nonwoven fabric, can be used.

  In forming the pressure-sensitive adhesive layer on the substrate sheet, a direct coating method in which the active energy ray-curable pressure-sensitive adhesive composition is directly applied to the substrate sheet or an active energy ray-curable pressure-sensitive adhesive composition is applied to the separator. Examples thereof include a transfer coating method in which the substrate sheet is bonded to the substrate sheet after the processing.

  The active energy ray-curable pressure-sensitive adhesive composition is usually applied after adjusting to a viscosity suitable for coating with a solvent as required. The method for applying the active energy ray-curable pressure-sensitive adhesive composition to the base sheet or separator is not particularly limited. For example, spray, shower, dipping, roll, spin, curtain, flow, slit, die And wet coating methods such as gravure, comma, screen printing, ink jet printing, and print coating with a dispenser.

  When the coated active energy ray-curable composition contains a solvent, it is dried after coating. However, as a drying condition, the solvent in the coated active energy ray-curable composition is volatilized. A sufficient drying temperature and drying time may be set. The drying temperature is usually 40 to 100 ° C., particularly preferably 50 to 90 ° C., and the drying time is preferably 1 to 60 minutes in view of production suitability.

  In addition, when the active energy ray-curable pressure-sensitive adhesive composition is a solid or a high-viscosity liquid, the viscosity is not adjusted with a solvent, but the active energy ray-curable composition is heated to reduce the viscosity. A hot melt method of coating by a method can also be used.

  The active energy ray-curable pressure-sensitive adhesive composition of the present invention is applied to a substrate sheet, dried, and then crosslinked by irradiation with active energy rays to form a pressure-sensitive adhesive, and further a pressure-sensitive adhesive sheet.

  As for the active energy ray irradiation, in the direct coating method, the active energy ray-curable pressure-sensitive adhesive composition is applied to the base sheet and heated and dried, and then the active energy ray is irradiated, and then the separator is attached. Alternatively, the active energy ray-curable pressure-sensitive adhesive composition may be applied to the substrate sheet and heated and dried, and then a separator may be attached, and then active energy rays may be irradiated. On the other hand, in the transfer coating method, the active energy ray-curable pressure-sensitive adhesive composition is applied to the separator and heated and dried, and then irradiated with active energy rays, and then a substrate sheet may be bonded to the separator. After applying the active energy ray-curable pressure-sensitive adhesive composition and heating and drying, the base material sheet may be bonded, and then the active energy ray may be irradiated.

  As the above active energy rays, rays such as far ultraviolet rays, ultraviolet rays, near ultraviolet rays, infrared rays, electromagnetic waves such as X rays and γ rays, electron beams, proton rays, neutron rays, etc. can be used. Curing by ultraviolet irradiation is advantageous from the standpoint of availability of the device and price. In addition, when performing electron beam irradiation, it can harden | cure even without using a photoinitiator (C).

As a method of curing by ultraviolet irradiation, a high pressure mercury lamp that emits light in a wavelength range of 150 to 450 nm, an ultra high pressure mercury lamp, a carbon arc lamp, a metal halide lamp, a xenon lamp, a chemical lamp, an electrodeless discharge lamp, an LED lamp, or the like is used. 30 to 5,000 mJ / cm ² .
After the ultraviolet irradiation, heating can be performed as necessary to complete the curing.

  Moreover, although the thickness of the said adhesive layer formed on a base material sheet after active energy ray irradiation is set suitably according to a use, it is 5-300 micrometers normally, Preferably it is 10-250 micrometers. . If the thickness of the pressure-sensitive adhesive layer is too thin, the adhesive physical properties tend to be difficult to stabilize, and if it is too thick, adhesive residue tends to occur.

The pressure-sensitive adhesive of the present invention thus obtained has a dielectric constant of 7.0 or less, and is preferably 6.5 or less, more preferably 6.0 or less, from the viewpoint of suppressing malfunction of the touch panel. The lower limit of the dielectric constant is usually 1.0.
If the dielectric constant is too high, the capacitance between the electrodes mounted on the touch panel tends to increase and tends to cause a malfunction, and if it is too low, the capacitance tends to decrease and the detection sensitivity tends to decrease.

  Moreover, as adhesive force of the adhesive sheet of this invention, it is 0.1-100N / 25mm normally, More preferably, it is 0.5-75N / 25mm, More preferably, it is 1-50N / 25mm, Most preferably, it is 10-50N. / 25 mm, particularly preferably 17.5 to 50 N / 25 mm.

  Since the urethane (meth) acrylate of the present invention has a low dielectric constant, the dielectric constant of the active energy ray-curable composition of the present invention containing the urethane (meth) acrylate is also low, and the active energy ray-curable composition containing the active energy ray-curable composition is included. The pressure-sensitive adhesive composition and the pressure-sensitive adhesive obtained by curing the pressure-sensitive adhesive composition are useful as pressure-sensitive adhesives for optical members such as optical devices such as touch panels and optical recording media. It is suitably used for sealing applications.

  EXAMPLES Hereinafter, although an Example is given and this invention is demonstrated further more concretely, this invention is not limited to a following example, unless the summary is exceeded. In the examples, “parts” and “%” mean weight standards.

<Example 1>
[Synthesis of Urethane Acrylate (A-1)]
In a four-necked flask equipped with a thermometer, a stirrer, a water-cooled condenser, and a nitrogen gas blowing port, 12.6 g (0.057 mol) of isophorone diisocyanate, bifunctional polyester polyol (hydroxyl value 60.3 mg KOH / g, number average molecular weight) 2,000, oxygen atom content X in the repeating structural unit X = 0.26, polyvalent carboxylic acid component: 100% sebacic acid contained) 84.7 g (0.046 mol), dibutyltin dilaurate 0. After charging 02 g and reacting at 80 ° C. for 6 hours, 2.7 g (0.023 mol) of 2-hydroxyethyl acrylate and 0.04 g of 2,6-di-tert-butylcresol as a polymerization inhibitor were charged, The reaction was terminated at 0 ° C. for 3 hours, and the reaction was terminated when the residual isocyanate group reached 0.3%. Preparative (A-1) (weight average molecular weight (Mw); 30,000) was obtained.
The following evaluation was performed about the obtained urethane acrylate (A-1).

<Dielectric constant>
For 100 parts by weight of urethane acrylate (A-1), 43 parts by weight of ethyl acetate and 4 parts of 1-hydroxy-cyclohexyl-phenyl-ketone (BASF Japan Ltd .; “Irgacure 184”) as a photopolymerization initiator are uniformly added. Mixing was performed to obtain an active energy ray-curable composition.

(Preparation of test piece for dielectric constant measurement)
The active energy ray-curable composition obtained above was applied onto an untreated polyethylene terephthalate (PET) film (thickness 50 μm) using an applicator so that the film thickness after curing was 150 μm, The solvent was volatilized for 10 minutes in the dryer. Thereafter, the active energy ray-curable composition side is laminated from above with an untreated polyethylene terephthalate (PET) film (thickness 50 μm), and is applied to a tabletop UV irradiation device (“Conveyor type tabletop irradiation device” manufactured by iGraphics). A cured film cured by irradiating with ultraviolet rays from the laminate side under the conditions of 80 W / cm (high pressure mercury lamp) × 18 cmH × 2.04 m / min × 3 Pass (integrated irradiation amount 2,400 mJ / cm ² ) A test piece for measuring dielectric constant was obtained by cutting out to × 7 cm.

(Measuring method)
Using an HP4284A Precision LCR meter (manufactured by Agilent), the obtained test piece is sandwiched between electrodes, an electric field is applied at a frequency of 1 MHz, and the electric capacity is measured. The dielectric constant of the adhesive composition was calculated and evaluated as follows. The dielectric constant of the active energy ray-curable pressure-sensitive adhesive composition can be regarded as the dielectric constant of urethane (meth) acrylate contained in the active energy ray-curable pressure-sensitive adhesive composition.
(Evaluation criteria)
○: 7.0 or less ×; greater than 7.0

<Compatibility>
The urethane acrylate (A-1) and the following ethylenically unsaturated monomer were blended in a weight ratio of 1: 1, respectively, and mixed well, then the appearance of the blended liquid was observed and evaluated as follows.
(B-1) Aliphatic monomer: butyl acrylate (B-2) Aromatic monomer: Phenoxyethyl acrylate (B-3) Hydroxyl group-containing monomer: 4-hydroxybutyl acrylate (Evaluation criteria)
○: The blended liquid was uniform.
X: The compounding liquid was nonuniform.

  Subsequently, adhesiveness was evaluated about the active energy ray-curable adhesive composition containing urethane acrylate (A-1).

<Adhesiveness>
100 parts of urethane (meth) acrylate (A-1), 81 parts of phenoxyethyl acrylate as ethylenically unsaturated monomer (B), 1-hydroxy-cyclohexyl-phenyl-ketone as a photopolymerization initiator (manufactured by BASF Japan Ltd.) "Irgacure 184") 7.2 parts were mixed uniformly to obtain an active energy ray-curable pressure-sensitive adhesive composition.

(Preparation of adhesive sheet for measuring adhesive strength)
The obtained active energy ray-curable pressure-sensitive adhesive composition was applied to an easy-adhesion-treated polyethylene terephthalate (PET) film (thickness: 125 μm) using an applicator so that the film thickness after curing was 175 μm, and tabletop UV irradiation was performed. 80 W / cm (high pressure mercury lamp) × 18 cmH × 2.04 m / min × 3 Pass (accumulated irradiation amount 2,400 mJ / cm ² ) with an apparatus (“Graphic tabletop irradiation device” manufactured by Eye Graphics Co., Ltd.) The adhesive sheet for measuring adhesive force was obtained by irradiating with UV rays and curing.

(Test method)
The obtained pressure-sensitive adhesive sheet was cut to 25 mm × 100 mm, and then pressure-bonded to a glass plate as an adherend by reciprocating twice using a 2 kg rubber roller in an atmosphere of 23 ° C. and a relative humidity of 50%. Was made. After leaving this test piece for 30 minutes in the same atmosphere, a 180 degree peel test was performed at a peel rate of 0.3 m / min, and the adhesive strength (N / 25 mm) was measured and evaluated according to the following criteria.
(Evaluation criteria)
○: 17.5 N / 25 mm or more Δ; 10 N / 25 mm or more and less than 17.5 N / 25 mm ×: less than 10 N / 25 mm

<Example 2>
[Synthesis of Urethane Acrylate (A-2)]
In a four-necked flask equipped with a thermometer, a stirrer, a water-cooled condenser and a nitrogen gas inlet, 11.9 g (0.054 mol) of isophorone diisocyanate, a bifunctional polyester polyol (hydroxyl value 56.0 mgKOH / g, number average molecular weight) 2,000, oxygen atom content X in the repeating structural unit X = 0.34, polyvalent carboxylic acid component: containing 35 mol% sebacic acid) 85.6 g (0.043 mol), dibutyltin dilaurate as reaction catalyst After charging 02 g and reacting at 80 ° C. for 6 hours, 2.5 g (0.022 mol) of 2-hydroxyethyl acrylate and 0.04 g of 2,6-di-tert-butylcresol as a polymerization inhibitor were charged. The reaction was terminated at 3 ° C for 3 hours, and when the residual isocyanate group reached 0.3%, the reaction was terminated. (A-2) (weight average molecular weight (Mw); 38,000) was obtained.

  About the obtained urethane acrylate (A-2), it carried out similarly to Example 1, and evaluated dielectric property and compatibility. Moreover, also about the active energy ray-curable adhesive composition containing urethane acrylate (A-2), adhesiveness was evaluated like Example 1. FIG.

<Comparative Example 1>
[Synthesis of Urethane Acrylate (A′-1)]
In a four-necked flask equipped with a thermometer, a stirrer, a water-cooled condenser, and a nitrogen gas inlet, isophorone diisocyanate 11.8 g (0.053 mol), bifunctional polyester polyol (hydroxyl value 55.4 mg KOH / g, number average molecular weight) 2,000, oxygen atom content X in the repeating structural unit X = 0.37, polyvalent carboxylic acid component: containing 100 mol% adipic acid)) 85.7 g (0.042 mol), dibutyltin dilaurate 0 as reaction catalyst 0.02 g was charged and reacted at 80 ° C. for 6 hours. Then, 2.5 g (0.022 mol) of 2-hydroxyethyl acrylate and 0.04 g of 2,6-di-tert-butylcresol as a polymerization inhibitor were charged. The reaction was carried out at 60 ° C. for 3 hours. When the remaining isocyanate group reached 0.3%, the reaction was terminated, Over preparative (A'-1) (weight average molecular weight (Mw); 26,000) was obtained.

  About the obtained urethane acrylate (A'-1), it carried out similarly to Example 1, and evaluated dielectric property and compatibility. Further, the tackiness of the active energy ray-curable pressure-sensitive adhesive composition containing urethane acrylate (A′-1) was evaluated in the same manner as in Example 1.

<Comparative Example 2> [Synthesis of Urethane Acrylate (A'-2)]
Into a four-necked flask equipped with a thermometer, stirrer, water-cooled condenser and nitrogen gas inlet, 10.1 g (0.045 mol) of isophorone diisocyanate, bifunctional hydrogenated polybutadiene polyol (hydroxyl value 48.3 mgKOH / g, number (Average molecular weight 2,000) 87.7 g (0.038 mol), 0.02 g of dibutyltin dilaurate as a reaction catalyst was charged and reacted at 80 ° C. for 6 hours, and then 2.2 g (0.015 mol) of 4-hydroxybutyl acrylate ), 0.04 g of 2,6-di-tert-butylcresol was added as a polymerization inhibitor and reacted at 60 ° C. for 3 hours. The reaction was terminated when the residual isocyanate group reached 0.3%, and urethane acrylate (A′-2) (weight average molecular weight (Mw); 49,000) was obtained.

About the obtained urethane acrylate (A'-2), it carried out similarly to Example 1, and evaluated dielectric property and compatibility.
Next, 69 parts by weight of isodecyl acrylate as the ethylenically unsaturated monomer (B) and 1-hydroxy-cyclohexyl-phenyl-ketone (BASF Japan Stock) as the photopolymerization initiator with respect to 100 parts by weight of the urethane acrylate (A′-2) 6.8 parts of “Irgacure 184” manufactured by the company were uniformly mixed to obtain an active energy ray-curable pressure-sensitive adhesive composition, and the tackiness was evaluated in the same manner as in Example 1.

  The above evaluation results are shown in Table 1 below.

From the above evaluation results, it can be seen that the urethane acrylates of Examples 1 and 2 having a dielectric constant of 7.0 or less have a good blend liquid appearance with various ethylenically unsaturated monomers and are excellent in compatibility. Moreover, it turns out that the active energy ray hardening adhesive composition of Example 1 and 2 containing this urethane acrylate shows the outstanding adhesiveness.
On the other hand, the urethane (meth) acrylate of Comparative Example 1 having a dielectric constant exceeding 7.0 is excellent in compatibility, but has a high dielectric constant and is difficult to apply to an adhesive for optical members.
Moreover, although the urethane acrylate of Comparative Example 2 obtained by reacting a polybutadiene polyol instead of the polyester polyol has a dielectric constant of 7.0 or less, the urethane acrylate is inferior in compatibility to the examples. It can be seen that it is.

  Although the present invention has been described in detail and with reference to specific embodiments, it will be apparent to those skilled in the art that various changes and modifications can be made without departing from the spirit and scope of the invention. This application is based on a Japanese patent application filed on November 18, 2014 (Japanese Patent Application No. 2014-233837), the contents of which are incorporated herein by reference.

  Since the active energy ray-curable composition of the present invention has a low dielectric constant, the active energy ray-curable adhesive composition and the adhesive of the present invention containing the active energy ray-curable composition are, for example, an optical device such as a touch panel, an optical recording medium, and the like. It is useful as a pressure-sensitive adhesive for optical members, and is particularly suitably used for bonding touch panel structural members and for sealing organic EL displays.

Claims (10)

  It contains urethane (meth) acrylate (A), which is a reaction product of polyester-based polyol (a1), polyisocyanate (a2), and hydroxyl group-containing (meth) acrylate (a3), and the urethane (meth) acrylate (A). An active energy ray-curable composition having a dielectric constant of 7.0 or less. The active energy ray-curable composition according to claim 1, wherein the content X of the oxygen atom in the repeating structural unit of the polyester polyol (a1) is 0.35 or less. However, the content X is a value represented by the following formula (1).
X = 16c / (12a + b + 16c) (1)
a: Number of carbon atoms in the repeating structural unit of the polyester-based polyol (a1) b: Number of hydrogen atoms in the repeating structural unit of the polyester-based polyol (a1) c: In the repeating structural unit of the polyester-based polyol (a1) Number of oxygen atoms   The polyester-based polyol (a1) is a polycondensate of a polyvalent carboxylic acid component containing a polyvalent carboxylic acid having an alkylene group having 5 to 20 carbon atoms and a polyhydric alcohol component. An active energy ray-curable composition.   The active energy ray-curable composition according to any one of claims 1 to 3, wherein the polyester-based polyol (a1) has a number average molecular weight of 500 to 12,000.   The weight average molecular weight of the said urethane (meth) acrylate (A) is 1,000-100,000, The active energy ray-curable composition of any one of Claims 1-4.   The active energy ray-curable composition according to any one of claims 1 to 5, further comprising an ethylenically unsaturated monomer (B) (excluding the urethane (meth) acrylate (A)).   An active energy ray-curable pressure-sensitive adhesive composition containing the active energy ray-curable composition according to any one of claims 1 to 6.   A pressure-sensitive adhesive obtained by curing the active energy ray-curable pressure-sensitive adhesive composition according to claim 7.   The adhesive sheet by which the adhesive of Claim 8 was laminated | stacked on the base material sheet.   Polyester polyol (a1), polyisocyanate (a2), and hydroxyl group-containing (meta) which is a polycondensate of a polyhydric carboxylic acid component containing a polyhydric carboxylic acid having an alkylene group having 5 to 20 carbon atoms and a polyhydric alcohol component ) Urethane (meth) acrylate which is a reaction product of acrylate (a3).