WO2016170875A1 - 紫外線硬化型粘着シート、及び、粘着シート - Google Patents
紫外線硬化型粘着シート、及び、粘着シート Download PDFInfo
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- WO2016170875A1 WO2016170875A1 PCT/JP2016/058104 JP2016058104W WO2016170875A1 WO 2016170875 A1 WO2016170875 A1 WO 2016170875A1 JP 2016058104 W JP2016058104 W JP 2016058104W WO 2016170875 A1 WO2016170875 A1 WO 2016170875A1
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- sensitive adhesive
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- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
- C09J133/00—Adhesives based on homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides, or nitriles thereof; Adhesives based on derivatives of such polymers
- C09J133/04—Homopolymers or copolymers of esters
- C09J133/06—Homopolymers or copolymers of esters of esters containing only carbon, hydrogen and oxygen, the oxygen atom being present only as part of the carboxyl radical
- C09J133/062—Copolymers with monomers not covered by C09J133/06
- C09J133/066—Copolymers with monomers not covered by C09J133/06 containing -OH groups
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- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
- C09J7/00—Adhesives in the form of films or foils
- C09J7/10—Adhesives in the form of films or foils without carriers
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
- C09J4/00—Adhesives based on organic non-macromolecular compounds having at least one polymerisable carbon-to-carbon unsaturated bond ; adhesives, based on monomers of macromolecular compounds of groups C09J183/00 - C09J183/16
- C09J4/06—Organic non-macromolecular compounds having at least one polymerisable carbon-to-carbon unsaturated bond in combination with a macromolecular compound other than an unsaturated polymer of groups C09J159/00 - C09J187/00
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- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
- C09J11/00—Features of adhesives not provided for in group C09J9/00, e.g. additives
- C09J11/02—Non-macromolecular additives
- C09J11/06—Non-macromolecular additives organic
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- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
- C09J133/00—Adhesives based on homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides, or nitriles thereof; Adhesives based on derivatives of such polymers
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
- C09J7/00—Adhesives in the form of films or foils
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
- C09J2301/00—Additional features of adhesives in the form of films or foils
- C09J2301/30—Additional features of adhesives in the form of films or foils characterized by the chemical, physicochemical or physical properties of the adhesive or the carrier
- C09J2301/312—Additional features of adhesives in the form of films or foils characterized by the chemical, physicochemical or physical properties of the adhesive or the carrier parameters being the characterizing feature
Definitions
- the present invention relates to an ultraviolet curable pressure-sensitive adhesive sheet that can be suitably used for production of IT-related products.
- a touch panel is installed in a mobile terminal such as a smartphone or a tablet.
- the touch panel includes a cover glass, an electrode glass / film, and a liquid crystal panel laminate.
- OCA Optical Clear Adhesive
- a smartphone a decorative layer is provided on a cover glass, and a step of about 20 ⁇ m is formed. Therefore, the OCA needs to adhere to the cover glass while following the step.
- the design of smartphones has increased and the decorative layer has become thicker to about 60 ⁇ m.
- the distortion is large, and the OCA is required to have a performance capable of following a thicker step or distortion.
- the ability to follow large steps without increasing the thickness of the OCA in order to enable both the thickness of the mobile terminal as a whole and the thickness of the decorative layer to be increased. Is required.
- UV curable pressure-sensitive adhesive composition examples include a pressure-sensitive adhesive obtained by using a solventless pressure-sensitive adhesive composition containing urethane acrylate, an acrylic monomer, and a photopolymerization initiator. (For example, see Patent Document 1).
- the step following property is good, but if the pressure-sensitive adhesive is excessively soft, it flows during heating and entrains bubbles. And sticking out of the adhesive and non-uniform film thickness.
- the problem to be solved by the present invention is to provide an ultraviolet curable pressure-sensitive adhesive sheet that is excellent in level-step following property, sheet holding property and moisture heat whitening resistance, and has no adhesive residue on the blade during cutting.
- the present invention includes an acrylic resin (A) having a hydroxyl group and / or a carboxyl group, a crosslinking agent (B), a (meth) acrylic compound (C) having two or more (meth) acryloyl groups, an organic solvent (D), And an ultraviolet curable pressure-sensitive adhesive sheet obtained by applying a pressure-sensitive adhesive composition containing a photopolymerization initiator (E) to release paper and drying the organic solvent (D), the ultraviolet curable pressure-sensitive adhesive sheet
- An ultraviolet curable pressure-sensitive adhesive sheet characterized by having a storage elastic modulus measured under conditions of a temperature of 20 ° C. and a frequency of 10 ⁇ 7 Hz is more than 5 ⁇ 10 3 Pa and not more than 1 ⁇ 10 5 Pa It is.
- the present invention also provides a pressure-sensitive adhesive sheet obtained by ultraviolet-curing the ultraviolet curable pressure-sensitive adhesive sheet.
- the UV curable pressure-sensitive adhesive sheet of the present invention is excellent in step followability, sheet retention and moisture and heat whitening resistance, and has no adhesive residue on the blade during punching (hereinafter abbreviated as “die cut property”). Therefore, the ultraviolet curable pressure-sensitive adhesive sheet of the present invention can be suitably used as an optical member, and particularly suitable for the manufacture of IT-related products such as touch panels, liquid crystal displays, plasma displays, organic EL, personal computers, and mobile phones. Can be used.
- the ultraviolet curable pressure-sensitive adhesive sheet of the present invention includes an acrylic resin (A) having a hydroxyl group and / or a carboxyl group, a crosslinking agent (B), a (meth) acrylic compound (C) having two or more (meth) acryloyl groups,
- the pressure-sensitive adhesive composition containing the organic solvent (D) and the photopolymerization initiator (E) is applied to release paper, and the organic solvent (D) is dried.
- the storage elastic modulus measured under the condition of 10 ⁇ 7 Hz is more than 5 ⁇ 10 3 Pa and not more than 1 ⁇ 10 5 Pa.
- the adhesive When the elastic modulus of the UV curable adhesive sheet measured at 20 ° C. and a frequency of 10 ⁇ 7 Hz is 5 ⁇ 10 3 Pa or less, the adhesive is very flexible and the initial tack is too high. For this reason, since the pressure-sensitive adhesive sheet cannot maintain its shape when the punching blade and the pressure-sensitive adhesive come into contact with each other during the punching process, the die-cutting property becomes poor, and when it exceeds 1 ⁇ 10 5 Pa, the adhesive strength is very weak. Therefore, the pressure-sensitive adhesive is slippery at the interface with the separator and the removal position cannot be fixed, resulting in poor die-cutting properties.
- the elastic modulus of the ultraviolet curable pressure-sensitive adhesive sheet is in the range of 6 ⁇ 10 3 to 5 ⁇ 10 4 Pa from the viewpoint that the die-cutting property can be further improved by imparting appropriate flexibility and adhesiveness to the pressure-sensitive adhesive. It is more preferable that
- the acrylic resin (A) having a hydroxyl group and / or a carboxyl group is an essential component for thermally cross-linking with a crosslinking agent (B) described later and exhibiting excellent sheet retention.
- the acrylic resin (A) include (meth) acrylic acid alkyl ester (a-1), (meth) acrylic compound (a-2) having a hydroxyl group and / or (meth) acrylic compound having a carboxyl group. Those obtained by polymerizing the (meth) acrylic compound (a) having (a-3) as an essential component can be used.
- the number of carbon atoms of the alkyl group of the (meth) acrylic acid alkyl ester (a-1) is in the range of 1 to 20 from the viewpoint of easy availability of raw materials and good adhesive strength.
- the range of 2 to 12 is more preferable, and the range of 4 to 8 is more preferable.
- (meth) acrylic acid alkyl ester (a-1) include, for example, methyl (meth) acrylate, ethyl (meth) acrylate, n-butyl (meth) acrylate, i-butyl (meth) acrylate, t -Butyl (meth) acrylate, n-propyl (meth) acrylate, n-hexyl (meth) acrylate, 2-ethylhexyl (meth) acrylate, n-octyl (meth) acrylate, isodecyl (meth) acrylate, lauryl (meth) acrylate , Tetradecyl (meth) acrylate, cetyl (meth) acrylate, stearyl (meth) acrylate, cyclohexyl (meth) acrylate, isobornyl (meth) acrylate, dicyclopentanyl (meth) acrylate
- These compounds may be used alone or in combination of two or more.
- the amount of the (meth) acrylic acid alkyl ester (a-1) used is in the range of 50 to 99.5% by mass in the (meth) acrylic compound (a) from the viewpoint of obtaining good adhesive strength.
- the range of 60 to 97% by mass is more preferable.
- Examples of the (meth) acrylic compound (a-2) having a hydroxyl group include 2-hydroxyethyl (meth) acrylate, 2-hydroxypropyl (meth) acrylate, 3-hydroxypropyl (meth) acrylate, and 2-hydroxybutyl.
- (Meth) acrylate 4-hydroxybutyl (meth) acrylate, 2-hydroxyhexyl (meth) acrylate, 6-hydroxyhexyl (meth) acryl, 8-hydroxyoctyl (meth) acrylate, 10-hydroxydecyl (meth) acrylate, 12-hydroxylauryl (meth) acrylate, polyoxyethylene (meth) acrylate, polyoxypropylene (meth) acrylate, glycerol (meth) acrylate, and the like can be used. These compounds may be used alone or in combination of two or more.
- the amount used in the case of using the (meth) acrylic compound (a-2) having a hydroxyl group is such that a good cross-linking reaction with the cross-linking agent (C) is formed, and good adhesive strength and sheet retention are obtained. Therefore, the content is preferably in the range of 0.001 to 20% by mass in the (meth) acrylic compound (a), and more preferably in the range of 0.01 to 5% by mass.
- Examples of the (meth) acrylic compound (a-3) having a carboxyl group include (meth) acrylic acid, carboxyethyl (meth) acrylate, carboxypentyl (meth) acrylate, and the like. These compounds may be used alone or in combination of two or more. Among these, when adjusting the glass transition temperature of acrylic resin (A), it is preferable to use (meth) acrylic acid from the point which has the outstanding cohesion force derived from a high glass transition temperature.
- the content is preferably in the range of 0.001 to 20% by mass and more preferably in the range of 0.01 to 5% by mass in the (meth) acrylic compound (a).
- acrylic resin (A) When obtaining the acrylic resin (A), other vinyl compounds may be used in combination with the (meth) acrylic compound (a) as necessary.
- Examples of the other vinyl compounds include vinyl acetate, vinyl propionate, vinyl laurate, styrene, chlorostyrene, chloromethylstyrene, ⁇ -methylstyrene, other substituted styrenes, methyl vinyl ether, ethyl vinyl ether, isobutyl vinyl ether, and the like. Can be used. These compounds may be used alone or in combination of two or more.
- Examples of the method for producing the acrylic resin (A) include a radical polymerization method resulting from the polymerizable double bond of the (meth) acrylic compound (a).
- the (meth) acrylic compound (a), if necessary, the other vinyl compound, and a radical polymerization initiator are preferably mixed and stirred at a temperature of 40 to 90 ° C. to perform radical polymerization. The method of advancing is mentioned.
- polymerization initiator examples include inorganic peroxides such as hydrogen peroxide, potassium persulfate, sodium persulfate, and ammonium persulfate; benzoyl peroxide, t-butylperoxy-2-ethylhexanoate, cumene hydroper Organic peroxides such as oxides; 2,2′-azobis- (2-aminodipropane) dihydrochloride, 2,2′-azobis- (N, N′-dimethyleneisobutylamidine) dihydrochloride, 2, 2′-azobis ⁇ 2-methyl-N- [1,1-bis (hydroxymethyl) -2-hydroxyethyl] propionamide ⁇ , azobisisobutyronitrile, 2,2′-azobis (2-methylbutyro An azo compound such as (nitrile) can be used.
- inorganic peroxides such as hydrogen peroxide, potassium persulfate, sodium persulfate, and ammonium persul
- the amount used in the case of using the polymerization initiator is preferably in the range of 0.001 to 5% by mass in the charged raw material of the acrylic resin (A) from the viewpoint of obtaining good polymerizability.
- the glass transition temperature of the acrylic resin (A) it is easy to adjust the storage elastic modulus measured under the conditions of the temperature of the ultraviolet curable pressure-sensitive adhesive sheet at 20 ° C. and the frequency of 10 ⁇ 7 Hz to the range specified in the present invention.
- the range is preferably ⁇ 50 to ⁇ 30 ° C., more preferably ⁇ 49 to ⁇ 40 ° C., and still more preferably ⁇ 48 to ⁇ 40 ° C. If the glass transition temperature of the acrylic resin (A) is within such a range, good die-cutting properties can be obtained while maintaining the flexibility and initial tack required when following a printing step.
- the glass transition temperature of the said acrylic resin (A) points out each glass transition temperature (the intermediate point glass transition temperature at the time of forming a homopolymer) of the (meth) acryl compound (a) which is a raw material, and another vinyl compound. )),
- the calculated value calculated by the Fox equation is shown.
- the weight average molecular weight of the acrylic resin (A) is preferably in the range of 200,000 to 2,000,000 from the viewpoint of imparting durability in practical use. From the viewpoint of coating suitability such as imparting properties, the range of 200,000 to 800,000 is more preferable, and the range of 200,000 to 500,000 is more preferable. In addition, the weight average molecular weight of the said acrylic resin (A) shows the value measured on condition of the following by the gel permeation chromatography (GPC) method.
- GPC gel permeation chromatography
- Measuring device High-speed GPC device (“HLC-8220GPC” manufactured by Tosoh Corporation) Column: The following columns manufactured by Tosoh Corporation were connected in series. "TSKgel G5000" (7.8 mm ID x 30 cm) x 1 "TSKgel G4000” (7.8 mm ID x 30 cm) x 1 "TSKgel G3000” (7.8 mm ID x 30 cm) x 1 “TSKgel G2000” (7.8 mm ID ⁇ 30 cm) ⁇ 1 detector: RI (differential refractometer) Column temperature: 40 ° C Eluent: Tetrahydrofuran (THF) Flow rate: 1.0 mL / min Injection amount: 100 ⁇ L (tetrahydrofuran solution with a sample concentration of 0.4 mass%) Standard sample: A calibration curve was prepared using the following standard polystyrene.
- the crosslinking agent (B) is thermally step-crosslinked with the hydroxyl group and carboxyl group of the acrylic resin (A) when the organic solvent (D) described later is dried, and has excellent step following property, sheet retention property, die cut property, and moisture resistance.
- a polyisocyanate crosslinking agent, an epoxy crosslinking agent, a chelate crosslinking agent, and a melamine crosslinking agent can be used. These crosslinking agents may be used alone or in combination of two or more.
- polyisocyanate crosslinking agent examples include polyisocyanates such as tolylene diisocyanate, chlorophenylene diisocyanate, hexamethylene diisocyanate, tetramethylene diisocyanate, xylylene diisocyanate, isophorone diisocyanate, diphenylmethane diisocyanate, hydrogenated diphenylmethane diisocyanate; and these trimethylolpropanes. Adducts; these isocyanurate bodies; these burette bodies and the like can be used. These crosslinking agents may be used alone or in combination of two or more.
- epoxy crosslinking agent examples include bisphenol A / epichlorohydrin type epoxy resin, ethylene glycol diglycidyl ether, polyethylene glycol diglycidyl ether, glycerin diglycidyl ether, glycerin triglycidyl ether, 1,6-hexanediol diglycidyl ether, Trimethylolpropane triglycidyl ether, sorbitol polyglycidyl ether, polyglycerol polyglycidyl ether, pentaerythritol polyglycidyl erythritol, diglycerol polyglycidyl ether, 1,3-bis (N, N-diglycidylaminomethyl) cyclohexane, N, N , N ′, N′-tetraglycidyl-m-xylenediamine or the like can be used. These crosslinking agents may be used alone or in combination of two or more.
- chelate crosslinking agent examples include acetylacetone coordination compounds of polyvalent metals such as aluminum, iron, copper, zinc, tin, titanium, nickel, antimony, magnesium, vanadium, chromium, zirconium; acetoacetate coordination compounds, etc. Can be used. These crosslinking agents may be used alone or in combination of two or more.
- melamine crosslinking agent examples include hexamethoxymethyl melamine, hexaethoxymethyl melamine, hexapropoxymethyl melamine, hexabutoxymethyl melamine, hexapentyloxymethyl melamine, hexahexyloxymethyl melamine, and the like. These crosslinking agents may be used alone or in combination of two or more.
- the amount of the crosslinking agent (B) used is 0.01 to 10 parts by mass with respect to 100 parts by mass of the acrylic resin (A) because the balance between the step following property and the sheet holding property can be further improved.
- the range is preferably 0.05 to 5 parts by mass.
- the (meth) acrylic compound (C) having two or more (meth) acryloyl groups forms a cross-linked structure with each other when the ultraviolet curable pressure-sensitive adhesive sheet is irradiated with ultraviolet rays. Since the cohesive force of the acrylic resin (A) by drawing is improved, excellent moisture and heat whitening resistance and other durability can be imparted.
- the (meth) acrylic compound (C) include ethylene glycol di (meth) acrylate, propylene glycol di (meth) acrylate, tetramethylene glycol di (meth) acrylate, trimethylolpropane di (meth) acrylate, and hexamethylene.
- (meth) acrylic compounds may be used alone or in combination of two or more.
- a (meth) acrylic compound having 2 to 6 (meth) acryloyl groups from the viewpoint of further improving wet heat and whitening resistance and die-cutting properties due to polymerizability.
- a (meth) acrylic compound having four (meth) acryloyl groups is more preferable to use a (meth) acrylic compound having four (meth) acryloyl groups.
- (meth) acrylic having an oxyalkylene group is highly polar and has improved compatibility with the acrylic resin (A) and / or cross-linking agent (B), resulting in more excellent moisture and heat whitening resistance.
- the average addition mole number of the oxyalkylene group is preferably in the range of 1 to 50 mol, more preferably in the range of 4 to 45 mol in the (meth) acrylic compound for the same reason.
- the content of the (meth) acrylic compound (C) is 0.5 to 60 parts by mass with respect to 100 parts by mass of the acrylic resin (A) from the viewpoint of further improving heat and heat whitening resistance and die cutting properties.
- the range is preferably 1 to 50 parts by mass.
- organic solvent (D) examples include toluene, ethyl acetate, butyl acetate, methyl ethyl ketone, hexane, acetone, cyclohexanone, 3-pentanone, acetonitrile, propionitrile, isobutyronitrile, valeronitrile, dimethyl sulfoxide, dimethylformamide. Etc. can be used. These organic solvents may be used alone or in combination of two or more.
- the amount of the organic solvent (D) used is preferably 80% by mass or less in the pressure-sensitive adhesive composition from the viewpoint of further improving the drying property and coating property, and more preferably in the range of 5 to 70% by mass. preferable.
- the photopolymerization initiator (E) generates radicals by light irradiation, heating, or the like, and initiates radical polymerization between the (meth) acrylic compounds (A).
- Examples of the photopolymerization initiator (E) include 4-phenoxydichloroacetophenone, diethoxyacetophenone, 2-hydroxy-2-methyl-1-phenylpropan-1-one, and 1- (4-isopropylphenyl) -2.
- Anthraquinone compounds such as 2,4,6-trimethylbenzoyldiphenylphosphine oxide and bis (2,4,6-trimethylbenzoyl) -phenylphosphine oxide; 3,3 ′, 4,4′- Tetra (tert-butylperoxycarbonyl) benzophenone, acrylated benzophenone, or the like can be used.
- These photopolymerization initiators may be used alone or in combination of two or more.
- photopolymerization initiator (E) 2-hydroxy-2-methyl-1-phenylpropan-1-one, 1-hydroxycyclohexyl phenyl ketone, 4,6-trimethylbenzoyldiphenylphosphine oxide and one or more photopolymerization initiators selected from the group consisting of bis (2,4,6-trimethylbenzoyl) -phenylphosphine oxide are preferably used. 6-trimethylbenzoyldiphenylphosphine oxide is more preferred.
- the amount of the photopolymerization initiator (E) used is preferably in the range of 0.01 to 5 parts by mass in the pressure-sensitive adhesive composition from the viewpoint of further improving the ultraviolet curability.
- the range of parts by mass is more preferable.
- the pressure-sensitive adhesive composition used in the present invention may contain other additives as necessary.
- additives examples include a silane coupling agent, an antioxidant, a light stabilizer, a rust inhibitor, a thixotropic agent, a sensitizer, a polymerization inhibitor, a leveling agent, a tackifier, and an antistatic agent.
- a flame retardant or the like can be used. These additives may be used alone or in combination of two or more.
- the viscosity of the pressure-sensitive adhesive composition used in the present invention is preferably in the range of 500 to 30,000 mPa ⁇ s and more preferably in the range of 1,000 to 20,000 mPa ⁇ s from the viewpoints of coatability and workability. More preferred.
- the said viscosity shows the value measured with the B-type viscometer at 25 degreeC.
- the ultraviolet curable pressure-sensitive adhesive sheet is obtained by coating the pressure-sensitive adhesive composition on release paper, drying the organic solvent (D), and then aging as necessary.
- the acrylic resin (A) and the cross-linking agent (B) are thermally cross-linked, so that excellent adhesiveness, step following ability, die-cutting property and sheet holding property are obtained.
- Examples of the method of applying the pressure-sensitive adhesive composition to release paper include a method of applying using an applicator, roll coater, knife coater, gravure coater, slot die coater, lip coater, and the like.
- Examples of the drying of the organic solvent (D) include a method of carrying out at a temperature of 60 to 120 ° C. for 1 minute to 1 hour.
- aging is performed at a temperature of 10 to 40 ° C. for 1 to 7 days. You may go.
- the thickness of the ultraviolet curable pressure-sensitive adhesive sheet is appropriately determined depending on the intended use, and is, for example, in the range of 10 to 500 ⁇ m.
- the storage elastic modulus of the ultraviolet curable pressure-sensitive adhesive sheet measured at 20 ° C. and a frequency of 1 Hz is preferably in the range of 5 ⁇ 10 3 to 5 ⁇ 10 5 Pa.
- the pressure is 5 ⁇ 10 3 Pa or more, the yield increases because the adhesive does not cause dimensional errors due to sheet holding during transportation and storage of the adhesive from the release film, and deformation of the sheet during bonding with the panel.
- difference in a release film can be suppressed.
- the sheet holding property is further improved, the range of 1 ⁇ 10 4 Pa to 5 ⁇ 10 5 Pa is preferable. Further, since it can secure an appropriate adhesion to the adherend, 5 ⁇ 10 4 to 5 ⁇ A range of 10 5 Pa is more preferable.
- the measuring method of the said storage elastic modulus of the said ultraviolet curable adhesive sheet is described in an Example.
- the storage elastic modulus of the ultraviolet curable pressure-sensitive adhesive sheet measured under the conditions of a temperature of 20 ° C. and a frequency of 10 ⁇ 6 Hz is in the range of 1 ⁇ 10 3 to 5 ⁇ 10 4 Pa.
- the range of 2 ⁇ 10 3 to 5 ⁇ 10 4 Pa is more preferable.
- the measuring method of the said storage elastic modulus of the said ultraviolet curable adhesive sheet is described in an Example.
- the tensile strength at an elongation of 60% in the tensile test measured under the conditions of a temperature of 25 ° C. and a tensile speed of 300 mm / min of the UV curable pressure-sensitive adhesive sheet is that it can be adhered at a low load by reducing the initial elastic modulus. From the viewpoint of further improving the printing step followability by increasing the agent deformation amount, it is preferably 7N or less, more preferably in the range of 2 to 7N.
- the pressure sensitive adhesive sheet is obtained by ultraviolet curing the ultraviolet curable pressure sensitive adhesive sheet.
- the ultraviolet irradiation is, for example, a method of irradiating the ultraviolet curable pressure-sensitive adhesive sheet with ultraviolet rays in a state having release paper; and bonding both surfaces of the ultraviolet curable pressure-sensitive adhesive sheet from which the release paper has been peeled, to at least two adherends; Next, a method of irradiating with ultraviolet rays; a method of attaching an ultraviolet curable pressure-sensitive adhesive sheet from which a release paper has been peeled off to one adherend, then irradiating with ultraviolet rays, and then attaching another adherend to the substrate.
- Examples of the adherend include, for example, a plastic substrate, a flexible printed substrate, a glass substrate, a substrate obtained by performing a release treatment on these substrates, a substrate on which ITO (indium tin oxide) is deposited, a touch panel, A liquid crystal module, a cover glass, a cover glass-touch panel integrated panel (OGS), or the like can be used. Etc. can be used. In addition, you may use the same to-be-adhered body for both surfaces of an ultraviolet curable adhesive sheet, or a separate to-be-adhered body, respectively.
- plastic substrate examples include acrylic resin, PC (polycarbonate), PBT (polybutylene terephthalate), PPS (polyphenylene sulfide), modified PPE (polyphenylene ether), PET (polyethylene terephthalate), COP (cycloolefin polymer),
- TAC triacetylcellulose
- an antireflection film, an antifouling film, a transparent conductive film constituting a touch panel, or the like can be used.
- the said adherend may have a level
- the step following property of the present invention is excellent, and the step having a thickness of 1 / 1.5 to 1/3, more preferably 1/2 to 1/3 of the thickness of the pressure-sensitive adhesive layer. It is also effective against Conventionally, the step following ability with respect to the thickness of about 1/5 to 1/10 with respect to the thickness of the pressure-sensitive adhesive layer has been discussed, so this effect is very excellent.
- the adhesive sheet of this invention is used for manufacture of IT related products, for example, liquid crystal module / adhesive sheet / touch panel, liquid crystal module / adhesive sheet / touch panel / adhesive sheet / cover glass, liquid crystal module / adhesive sheet / OGS and the like.
- Examples of the ultraviolet irradiation method include a method using a known ultraviolet light irradiation device such as a xenon lamp, a xenon-mercury lamp, a metal halide lamp, a high pressure mercury lamp, or a low pressure mercury lamp.
- a known ultraviolet light irradiation device such as a xenon lamp, a xenon-mercury lamp, a metal halide lamp, a high pressure mercury lamp, or a low pressure mercury lamp.
- the irradiation dose of the ultraviolet preferably be 0.05 ⁇ 5J / cm 2, more preferably 0.1 ⁇ 3J / cm 2, particularly preferably in the range of 0.3 ⁇ 1.5J / cm 2 Good.
- the irradiation amount of ultraviolet rays is based on a value measured in a wavelength range of 300 to 390 nm using a UV checker “UVR-N1” manufactured by GS Yuasa Corporation.
- the (meth) acrylic compound (C) is completely cured and the crosslink density is improved, so that excellent die-cutting properties and wet heat whitening resistance are exhibited.
- the storage elastic modulus of the pressure-sensitive adhesive sheet measured under the conditions of a temperature of 20 ° C. and a frequency of 1 Hz is in the range of 1 ⁇ 10 4 to 1 ⁇ 10 6 Pa, such as high temperature, high temperature and high humidity, and a cooling / heating cycle.
- Durability such as heat-and-moisture whitening resistance can be further improved by providing high cohesive strength that does not cause foaming or cloudiness of the adhesive layer, lowering of adhesive strength, or misalignment of the laminate even in actual use under high load environment. Therefore, the range of 5 ⁇ 10 4 to 1 ⁇ 10 6 Pa is more preferable, and the range of 1 ⁇ 10 5 to 6 ⁇ 10 5 Pa is particularly preferable.
- the measuring method of the said storage elastic modulus of the said adhesive sheet is described in an Example.
- the storage elastic modulus of the pressure-sensitive adhesive sheet measured under the conditions of a temperature of 20 ° C. and a frequency of 10 ⁇ 7 Hz is in the range of 1 ⁇ 10 4 to 1 ⁇ 10 6 Pa.
- Durability such as heat-and-moisture whitening resistance can be further improved by providing a high cohesive force that does not cause foaming or cloudiness of the adhesive layer or misalignment of the laminate even under high load environments such as high humidity and cold cycles.
- the range of 1 ⁇ 10 4 to 5 ⁇ 10 5 Pa is more preferable, and the range of 1 ⁇ 10 4 to 1 ⁇ 10 5 Pa is particularly preferable.
- the measuring method of the said storage elastic modulus of the said adhesive sheet is described in an Example.
- the pressure-sensitive adhesive floats under normal temperature or after-loading environment when the pressure-sensitive adhesive strength is increased. From the point that problems such as peeling and foaming can be further suppressed, the range is preferably 100 N or more, more preferably 110 to 250 N, and particularly preferably 120 to 200 N.
- the measuring method of the said breaking strength of the said adhesive sheet is described in an Example.
- the range is preferably from 200 to 1,000%, more preferably from 300 to 900%.
- the measuring method of the said breaking strength of the said adhesive sheet is described in an Example.
- the ultraviolet curable pressure-sensitive adhesive sheet of the present invention is excellent in level difference followability, sheet retention, moisture heat whitening resistance, and die cutability. Therefore, the ultraviolet curable pressure-sensitive adhesive sheet of the present invention can be suitably used as an optical member, and particularly suitable for the manufacture of IT-related products such as touch panels, liquid crystal displays, plasma displays, organic EL, personal computers, and mobile phones. Can be used.
- acrylic resin (A′-1) having a nonvolatile content of 48.9% by mass, a viscosity of 4,460 mPa ⁇ s, a weight average molecular weight of 250,000, a number average molecular weight of 63,000, and a glass transition temperature of ⁇ 56.5 ° C. )
- Example 1 In a container equipped with a stirrer, a reflux condenser, and a thermometer, 100 parts by mass of the acrylic resin (A-1) obtained in Synthesis Example 1, propoxylated pentaerythritol tetraacrylate (average added mole number of oxypropylene group; 6 mol) Hereinafter, it is abbreviated as “propoxylated PETA”.) 20 parts by mass and 1 part by mass of 1-hydroxycyclohexyl ruphenyl ketone (“Irgacure 184” manufactured by BASF) were added and stirred until uniform.
- Irgacure 184 1-hydroxycyclohexyl ruphenyl ketone
- the pressure-sensitive adhesive composition was applied to the surface of a release polyethylene terephthalate film (hereinafter abbreviated as “release PET 50”) having a thickness of 50 ⁇ m so that the film thickness after drying with an organic solvent would be 100 ⁇ m. It was dried in a dryer at 3 ° C. for 3 minutes to obtain an ultraviolet curable pressure sensitive adhesive sheet.
- release PET 50 a release polyethylene terephthalate film having a thickness of 50 ⁇ m so that the film thickness after drying with an organic solvent would be 100 ⁇ m. It was dried in a dryer at 3 ° C. for 3 minutes to obtain an ultraviolet curable pressure sensitive adhesive sheet.
- Examples 2 to 7, Comparative Examples 1 to 4 Implemented except that the types and / or amounts of the acrylic resin (A), crosslinking agent (B), (meth) acrylic compound (C), and photopolymerization initiator (E) used were changed as shown in Tables 1 to 3 In the same manner as in Example 1, an adhesive composition and an ultraviolet curable adhesive sheet were obtained, and the storage elastic modulus of the ultraviolet curable adhesive sheet was measured.
- the frame having a thickness of 50 ⁇ m was placed on a glass plate, and the test piece was pasted by reciprocating 2 kg roll ⁇ 2 from above, and pasted so that the 50 ⁇ m frame was sandwiched between PET100 and the test piece. This was autoclaved in a 50 ° C. atmosphere at a pressure of 0.5 MPa for 20 minutes. Thereafter, UV irradiation was performed from the glass plate side so that the integrated light quantity of the wavelength in the UV-A region after passing through the glass was 1 J / cm 2 to obtain a test piece. The obtained test piece was allowed to stand in an 80 ° C. atmosphere for 24 hours, the inside of a 50 ⁇ m thick frame was visually observed, and the followability with respect to the 50 ⁇ m thickness was evaluated as follows. “ ⁇ ”: no floating from the step, no air bubbles. “ ⁇ ”: There is no floating from the level difference, and there is a part of bubbles. “ ⁇ ”: Bubbles mixed
- Deformation rate of sheet (%) [area (mm 2 ) ⁇ 400 (mm 2 ) of ultraviolet curable pressure-sensitive adhesive sheet after heating / pressing) / 400 (mm 2 ) “ ⁇ ”: 0%, “ ⁇ ”; more than 0% and less than 3%, “ ⁇ ”: 3% or more
- the ultraviolet curable pressure-sensitive adhesive sheets obtained in Examples and Comparative Examples were cut into a width of 50 mm and a length of 40 mm, and a float glass having a thickness of 1 mm, a width of 76 mm, and a length of 52 mm through the ultraviolet curable pressure-sensitive adhesive sheet, and a thickness A laminate was prepared by bonding together a polycarbonate plate with a hard coat having a thickness of 0.6 mm, a width of 80 mm, and a length of 50 mm to obtain a test piece.
- a turbidimeter “NDH5000” manufactured by Nippon Denshoku Industries Co., Ltd. haze and light transmittance were measured according to JIS K7361-1-1997.
- the degree of yellowing (b *) was measured using a spectrocolorimeter “CM-5000d” manufactured by Konica Minolta Sensing Co., Ltd. according to JIS K7105-1981 under conditions of a light source C and a visual field of 2 °. Further, the test piece was allowed to stand for 500 hours in an atmosphere having a temperature of 85 ° C. and a humidity of 85%, and then taken out in an atmosphere having a temperature of 23 ° C. and a humidity of 50%.
- Examples 1 to 7 which are the ultraviolet curable pressure-sensitive adhesive sheets of the present invention, are excellent in step followability, sheet retention, moisture and heat whitening resistance, and die cutability.
- Comparative Examples 1 to 4 are modes in which the storage elastic modulus of the ultraviolet curable pressure-sensitive adhesive sheet measured under the conditions of a temperature of 20 ° C. and a frequency of 10 ⁇ 7 Hz is below the range defined in the present invention. In addition, all of sheet retention, moisture heat whitening resistance and die cutability could not be satisfied.
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Abstract
Description
カラム:東ソー株式会社製の下記のカラムを直列に接続して使用した。
「TSKgel G5000」(7.8mmI.D.×30cm)×1本
「TSKgel G4000」(7.8mmI.D.×30cm)×1本
「TSKgel G3000」(7.8mmI.D.×30cm)×1本
「TSKgel G2000」(7.8mmI.D.×30cm)×1本
検出器:RI(示差屈折計)
カラム温度:40℃
溶離液:テトラヒドロフラン(THF)
流速:1.0mL/分
注入量:100μL(試料濃度0.4質量%のテトラヒドロフラン溶液)
標準試料:下記の標準ポリスチレンを用いて検量線を作成した。
東ソー株式会社製「TSKgel 標準ポリスチレン A-500」
東ソー株式会社製「TSKgel 標準ポリスチレン A-1000」
東ソー株式会社製「TSKgel 標準ポリスチレン A-2500」
東ソー株式会社製「TSKgel 標準ポリスチレン A-5000」
東ソー株式会社製「TSKgel 標準ポリスチレン F-1」
東ソー株式会社製「TSKgel 標準ポリスチレン F-2」
東ソー株式会社製「TSKgel 標準ポリスチレン F-4」
東ソー株式会社製「TSKgel 標準ポリスチレン F-10」
東ソー株式会社製「TSKgel 標準ポリスチレン F-20」
東ソー株式会社製「TSKgel 標準ポリスチレン F-40」
東ソー株式会社製「TSKgel 標準ポリスチレン F-80」
東ソー株式会社製「TSKgel 標準ポリスチレン F-128」
東ソー株式会社製「TSKgel 標準ポリスチレン F-288」
東ソー株式会社製「TSKgel 標準ポリスチレン F-550」
<アクリル樹脂(A-1)の合成>
攪拌機、還流冷却管、窒素導入管、温度計を備えた反応容器に、2-エチルヘキシルアクリレート(以下、「2EHA」と略記する。)73質量部、ジシクロペンタニルアクリレート(日立化成株式会社製「FA-513AS」)20質量部、アクリル酸(以下、「AA」と略記する。)5質量部、2-ヒドロキシエチルアクリレート(以下、「HEA」と略記する。)2質量部、酢酸エチル50質量部、トルエン50質量部を仕込み、攪拌下、窒素を吹き込みながら70℃まで昇温した。1時間後に、予め酢酸エチルにて溶解したアゾビスイソブチロニトリル溶液0.04質量部を添加した。その後、攪拌下70℃にて3時間ホールドした後、75℃に昇温し、テトラメチルブチルパーオキシエチルヘキサノエート0.2質量部、t-へキシルパーオキシピバレート1質量部を添加し5時間ホールドし、不揮発分50質量%、粘度8,540mPa・s、重量平均分子量44万、数平均分子量7.6万、ガラス転移温度-41.8℃のアクリル樹脂(A-1)を得た。
<アクリル樹脂(A-2)の合成>
攪拌機、還流冷却管、窒素導入管、温度計を備えた反応容器に、2EHAを73質量部、FA-513ASを20質量部、AAを5質量部、HEAを2質量部、酢酸エチル100質量部を仕込み、攪拌下、窒素を吹き込みながら70℃まで昇温した。1時間後に、予め酢酸エチルにて溶解したアゾビスイソブチロニトリル溶液0.04質量部を添加した。その後、攪拌下70℃にて3時間ホールドした後、75℃に昇温し、5時間ホールドし、不揮発分50質量%、粘度49,900mPa・s、重量平均分子量74万、数平均分子量9.3万、ガラス転移温度-41.8℃のアクリル樹脂(A-2)を得た。
<アクリル樹脂(A-3)の合成>
攪拌機、還流冷却管、窒素導入管、温度計を備えた反応容器に、2EHAを63質量部、シクロヘキシルアクリレート(以下、「CHA」と略記する。)を35質量部、4HBAを2質量部、酢酸エチル50質量部、トルエン50質量部を仕込み、攪拌下、窒素を吹き込みながら70℃まで昇温した。1時間後に、予め酢酸エチルにて溶解したアゾビスイソブチロニトリル溶液0.04部を添加した。その後、攪拌下65℃にて3時間ホールドした後、75℃に昇温し、5時間ホールドし、不揮発分50質量%、粘度8,650mPa・s、重量平均分子量41万、数平均分子量7.2万、ガラス転移温度-44.4℃のアクリル樹脂(A-3)を得た。
<アクリル樹脂(A-4)の合成>
攪拌機、還流冷却管、窒素導入管、温度計を備えた反応容器に、2EHAを73質量部、イソボルニルアクリレート(以下、「IBXA」と略記する。)を20質量部、AAを5質量部、HEAを2質量部、酢酸エチル50質量部、トルエン50質量部を仕込み、攪拌下、窒素を吹き込みながら70℃まで昇温した。1時間後に、予め酢酸エチルにて溶解したアゾビスイソブチロニトリル溶液0.04質量部を添加した。その後、攪拌下70℃にて3時間ホールドした後、75℃に昇温し、5時間ホールドし、不揮発分50.1質量%、粘度9,030mPa・s、重量平均分子量44万、数平均分子量7.4万、ガラス転移温度-43.5℃のアクリル樹脂(A-4)を得た。
<アクリル樹脂(A-5)の合成>
攪拌機、還流冷却管、窒素導入管、温度計を備えた反応容器に、2-EHAを55質量部、n-ブチルアクリレート(以下、「BA」と略記する。)を23質量部、IBXAを20質量部、4HBAを2質量部、酢酸エチル50質量部、トルエン50質量部を仕込み、攪拌下、窒素を吹き込みながら70℃まで昇温した。1時間後に、予め酢酸エチルにて溶解したアゾビスイソブチロニトリル溶液0.04質量部を添加した。その後、攪拌下70℃にて3時間ホールドした後、75℃に昇温し、5時間ホールドし、不揮発分50.2質量%、粘度9,480mPa・s、重量平均分子量43万、数平均分子量7.4万、ガラス転移温度-45.5℃のアクリル樹脂(A-5)を得た。
<アクリル樹脂(A-6)の合成>
攪拌機、還流冷却管、窒素導入管、温度計を備えた反応容器に、2EHAを55質量部、BAを28質量部、メチルメタクリレート(以下、「MMA」と略記する。)を20質量部、4HBAを2質量部、酢酸エチル50質量部、トルエン50質量部を仕込み、攪拌下、窒素を吹き込みながら70℃まで昇温した。1時間後に、予め酢酸エチルにて溶解したアゾビスイソブチロニトリル溶液0.04質量部を添加した。その後、攪拌下70℃にて3時間ホールドした後、75℃に昇温し、5時間ホールドし、不揮発分51.5質量%、粘度11,790mPa・s、重量平均分子量46万、数平均分子量7.5万、ガラス転移温度-49℃のアクリル樹脂(A-6)を得た。
<アクリル樹脂(A-7)の合成>
攪拌機、還流冷却管、窒素導入管、温度計を備えた反応容器に、2EHAを55質量部、MMAを20質量部、HEAを2質量部、酢酸エチル50質量部、トルエン50質量部を仕込み、攪拌下、窒素を吹き込みながら70℃まで昇温した。1時間後に、予め酢酸エチルにて溶解したアゾビスイソブチロニトリル溶液0.04質量部を添加した。その後、攪拌下70℃にて3時間ホールドした後、75℃に昇温し、5時間ホールドし、不揮発分50.2質量%、粘度17,760mPa・s、重量平均分子量37万、数平均分子量6.7万、ガラス転移温度-41.6℃のアクリル樹脂(A-7)を得た。
<アクリル樹脂(A’-1)の合成>
攪拌機、還流冷却管、窒素導入管、温度計を備えた反応容器に、2EHAを78質量部、BAを20質量部、4HBAを2質量部、トルエン100質量部を仕込み、攪拌下、窒素を吹き込みながら65℃まで昇温した。1時間後に、予め酢酸エチルにて溶解したアゾビスイソブチロニトリル溶液0.04質量部を添加した。その後、攪拌下65℃にて3時間ホールドした後、75℃に昇温し、テトラメチルブチルパーオキシエチルヘキサノエート0.2質量部、t-へキシルパーオキシピバレート1質量部を添加し5時間ホールドし、不揮発分48.9質量%、粘度4,460mPa・s、重量平均分子量25万、数平均分子量6.3万、ガラス転移温度-56.5℃のアクリル樹脂(A’-1)を得た。
<アクリル樹脂(A’-2)の合成>
攪拌機、還流冷却管、窒素導入管、温度計を備えた反応容器に、2EHAを70質量部、酢酸ビニル(以下、「VAc」と略記する。)25質量部、AAを5質量部、酢酸エチル50質量部、トルエン50質量部を仕込み、攪拌下、窒素を吹き込みながら70℃まで昇温した。1時間後に、予め酢酸エチルにて溶解したアゾビスイソブチロニトリル溶液0.04質量部を添加した。その後、攪拌下70℃にて3時間ホールドした後、75℃に昇温し、5時間ホールドし、不揮発分51.6質量%、粘度47,900mPa・s、重量平均分子量59万、数平均分子量7.9万、ガラス転移温度-50.1℃のアクリル樹脂(A’-2)を得た。
<アクリル樹脂(A’-3)の合成>
攪拌機、還流冷却管、窒素導入管、温度計を備えた反応容器に、2EHAを75質量部、VAcを20質量部、AAを5質量部、酢酸エチル50質量部、トルエン50部を仕込み、攪拌下、窒素を吹き込みながら70℃まで昇温した。1時間後に、予め酢酸エチルにて溶解したアゾビスイソブチロニトリル溶液0.04質量部を添加した。その後、攪拌下70℃にて3時間ホールドした後、75℃に昇温し、5時間ホールドし、不揮発分51.5質量%、粘度14,550mPa・s、重量平均分子量47万、数平均分子量9.6万、ガラス転移温度-46.1℃のアクリル樹脂(A’-3) を得た。
攪拌機、還流冷却管、温度計を備えた容器に、合成例1で得られたアクリル樹脂(A-1)100質量部、プロポキシ化ペンタエリスリトールテトラアクリレート(オキシプロピレン基の平均付加モル数;6モル、以下、「プロポキシ化PETA」と略記する。)20質量部、1-ヒドロキシシクロヘキシルーフェニルーケトン(BASF社製「Irgacure184」)1質量部を添加し、均一になるまで攪拌した。その後、200メッシュ金網で濾過し、エポキシ架橋剤(三菱ガス化学株式会社製「TETERAD-X」、以下、「EPO-1」と略記する。)を0.1質量部加え、粘着剤組成物を得た。
厚さ50μmの離型ポリエチレンテレフタラートフィルム(以下、「離型PET50」と略記する。)の表面に有機溶剤乾燥後の膜厚が100μmとなるように前記粘着剤組成物を塗工し、80℃乾燥機中で3分間乾燥させ、紫外線硬化型粘着シートを得た。
前記紫外線硬化型粘着シートを遮光下にて、厚さ1mmになるまで重ね合せ、アントン・パール社製動的粘弾性測定装置「MCR-302」を使用して、下記条件にて貯蔵弾性率を測定した。
測定温度;20~150℃
パラレルプレート;25mmΦ
角振動数;ω=500~0.005rad/sec
歪み量;3%
得られた温度別周波数分散結果から、周波数fをf(Hz)=ω/2πより計算し、20℃における10-9~101Hzの主は数分散のマスターカーブを作成し、貯蔵弾性率を抽出した。
用いるアクリル樹脂(A)、架橋剤(B)、(メタ)アクリル化合物(C)、並びに、光重合開始剤(E)の種類及/又は量を表1~3に示す通り変更した以外は実施例1と同様に粘着剤組成物、紫外線硬化型粘着シートを得、紫外線硬化型粘着シートの貯蔵弾性率を測定した。
実施例及び比較例で得られた紫外線硬化型粘着シートの片面を、厚さ100μmのポリエチレンテレフタラートフィルム(PET100)に貼り合せ、片面にPET100が貼り合わされた紫外線硬化型粘着シートを得た。これを縦50mm、横40mmに裁断したものを試験片とした。次に、厚さ50μmのポリエチレンテレフタラートフィルムから縦40mm、横30mm、幅5mmの枠を切り出した。この厚さ50μmの枠をガラス板の上に載置し、その上から前記試験片を2kgロール×2往復で貼付け、PET100と試験片で50μmの枠を挟むように貼り付けた。これを、50℃雰囲気下、0.5MPaの圧力で20分間オートクレーブ処理した。その後、ガラス板側からガラス透過後のUV-A領域の波長の積算光量が1J/cm2となるようにUV照射し、試験片を得た。得られた試験片を80℃雰囲気下に24時間放置し、50μm厚の枠の内側を目視にて観察し、50μm厚に対する追従性を以下のように評価した。
「○」;段差からの浮きなし、気泡の混入無し。
「△」;段差からの浮きなし、気泡の混入一部あり。
「×」;気泡の混入あり
実施例及び比較例で得られた紫外線硬化型粘着シートを、20mm辺の正方形に裁断し、両面の離型フィルムを剥離し、50mm辺の正方形の離型PET50に貼り合せ、更に2mm厚のガラス板で挟んだ後、40℃環境下1kg/cm2の荷重をかけ、24時間放置した。荷重を除いた直後にシート面積を測定し、シートの変形率を下記計算式(1)にて算出し、以下のように評価した。
シートの変形率(%)=[加温・加圧後の紫外線硬化型粘着シートの面積(mm2)-400(mm2)]/400(mm2)
「○」;0%、「△」;0%を超えて3%未満、「×」;3%以上
実施例及び比較例で得られた紫外線硬化型粘着シートを幅50mm、長さ40mmに裁断し、該紫外線硬化型粘着シートを介して、1mm厚、幅76mm、長さ52mmのフロートガラスと、厚さ0.6mm、幅80mm、長さ50mmのハードコート付きのポリカーボネート板を貼り合せて積層体を作製し試験片とした。これを、日本電色工業株式会社製濁度計「NDH5000」を使用して、JISK7361-1-1997に準じてヘイズ及び光線透過率を測定した。黄変度(b*)は、コニカミノルタセンシング株式会社製分光測色計「CM-5000d」を使用して、JISK7105-1981に準じて、光源C、視野2°の条件にて測定した。更に、前記試験片を温度85℃、湿度85%の雰囲気下で500時間放置した後、温度23℃、湿度50%の雰囲気下で取出した。取出し後、室温で12時間放置した後に、気泡の発生有無を目視観察し、前述した方法と同様に、ヘイズ、光線透過率及び黄変度を測定し、以下のように評価した。
「○」;気泡の発生なく、ヘイズ、黄変度の上昇も無く、光線透過率の低下も無し。
「△」;気泡の発生はないが、ヘイズ及び黄変度の僅かな上昇が確認され、光線透過率も±0.2以内の変化が確認された。
「×」;気泡の発生が確認され、又は、ヘイズ及び黄変度の上昇が確認され、かつ、光線透過率が±0.2を超える変化が確認された。
実施例及び比較例で得られた紫外線硬化型粘着シートを長さ300mm、幅110mmの大きさに裁断し、長さ方向にダイカット刃で長さ100mm、幅10mmの大きさで5mm間隔で20枚ハーフカットし、抜き刃への粘着層の付着有無を目視確認した。続いて、離型PET側を固定し、周辺部分の紫外線硬化型粘着シートを1,000mm/分の速度で90°剥離し、打ち抜かれた部分の剥離の有無及び粘着層のハミ出しの有無を目視確認し、以下のように評価した。
「○」;抜き刃への粘着層の付着、打ち抜き部分の剥離及びハミ出しがない。
「△」;抜き刃への粘着層の付着、打ち抜き部分の剥離及びハミ出しが僅かに確認される。
「×」;抜き刃への粘着層の付着、打ち抜き部分の剥離及びハミ出しが明らかに確認される。
実施例及び比較例で得られた紫外線硬化型粘着シートを遮光下にて厚さ500μmになるまで重ね合せ、A&D社製テンシロン引張強度試験機「RTF-1210」を使用して、10mm幅、標線間隔20mmの試験片を温度25℃、引張速度300mm/分の条件で長さ方向に引張り、伸度60%での引張強度(N)を測定した。
実施例及び比較例で得られた紫外線硬化型粘着シートを、UV-A領域の波長の積算光量が1J/cm2となるようにUV照射し、紫外線硬化した粘着シートを得た。得られた粘着シートを厚さ500μmになるまで重ね合せ、アントン・パール社製動的粘弾性測定装置「MCR-302」を使用して、下記条件にて貯蔵弾性率を測定した。
測定温度;20~150℃
パラレルプレート;25mmΦ
角振動数;ω=500~0.005rad/sec
歪み量;3%
得られた温度別周波数分散結果から、周波数fをf(Hz)=ω/2πより計算し、20℃における10-9~101Hzの主は数分散のマスターカーブを作成し、貯蔵弾性率を抽出した。
実施例及び比較例で得られた紫外線硬化型粘着シートをUV-A領域の波長の積算光量が1J/cm2となるようにUV照射し、紫外線硬化した粘着シートを得た。得られた粘着シートを厚さ500μmになるまで重ね合せ、A&D社製テンシロン引張強度試験機「RTF-1210」を使用して、10mm幅、標線間隔20mmの試験片を温度25℃、引張速度300mm/分の条件で長さ方向に引張り、破断強度(N)及び破断伸度(%)を測定した。
「XDIアダクト体」;キシリレンジイソシアネートのアダクト体
「MOI」;2-イソシアナートエチルメタクリレート(昭和電工株式会社製「カレンズMOI」)
「EsacureTZT」;2,4,6-トリメチルベンゾフェノン及び4-メチルベンゾフェノンの混合物(ランベルティ社製光重合開始剤「EsacureTZT」)
Claims (6)
- 水酸基及び/又はカルボキシル基を有するアクリル樹脂(A)、架橋剤(B)、2個以上の(メタ)アクリロイル基を有する(メタ)アクリル化合物(C)、有機溶剤(D)、及び、光重合開始剤(E)を含有する粘着剤組成物を剥離紙に塗工し、有機溶剤(D)を乾燥させて得られる紫外線硬化型粘着シートであって、前記紫外線硬化型粘着シートの温度20℃、周波数10-7Hzの条件で測定した貯蔵弾性率が、5×103Paを超えて1×105Pa以下であることを特徴とする紫外線硬化型粘着シート。
- 前記アクリル樹脂(A)のガラス転移温度が、-50~-30℃の範囲である請求項1記載の紫外線硬化型粘着シート。
- 温度20℃、周波数1Hzの条件で測定した貯蔵弾性率が、5×103~5×105Paの範囲であり、
温度20℃、周波数10-6Hzの条件で測定した貯蔵弾性率が、1×103~5×104Paの範囲である請求項1記載の紫外線硬化型粘着シート。 - 温度25℃、引張速度300mm/分の条件で測定した引張試験において、伸度60%における引張強度が7N以下である請求項1記載の紫外線硬化型粘着シート。
- 請求項1~4のいずれか1項記載の紫外線硬化型粘着シートを紫外線硬化して得られることを特徴とする粘着シート。
- 温度20℃、周波数1Hzの条件で測定した貯蔵弾性率が、1×104~1×106Paの範囲であり、
温度20℃、周波数10-7Hzの条件で測定した貯蔵弾性率が、1×104~1×106Paの範囲である請求項5記載の粘着シート。
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